CA2329475A1 - Fast cycle psa with adsorbents sensitive to atmospheric humidity - Google Patents

Fast cycle psa with adsorbents sensitive to atmospheric humidity Download PDF

Info

Publication number
CA2329475A1
CA2329475A1 CA002329475A CA2329475A CA2329475A1 CA 2329475 A1 CA2329475 A1 CA 2329475A1 CA 002329475 A CA002329475 A CA 002329475A CA 2329475 A CA2329475 A CA 2329475A CA 2329475 A1 CA2329475 A1 CA 2329475A1
Authority
CA
Canada
Prior art keywords
contaminant
gas
product
adsorbers
adsorbent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002329475A
Other languages
French (fr)
Inventor
Andrea Gibbs
Matthew Babicki
Surajit Roy
Bowie Keefer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
QuestAir Technologies Inc
Original Assignee
QuestAir Technologies Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by QuestAir Technologies Inc filed Critical QuestAir Technologies Inc
Priority to CA002329475A priority Critical patent/CA2329475A1/en
Priority to EP01991154A priority patent/EP1355717A4/en
Priority to AU2002230897A priority patent/AU2002230897A1/en
Priority to US10/021,751 priority patent/US7037358B2/en
Priority to CNB018204244A priority patent/CN100371051C/en
Priority to CA002430156A priority patent/CA2430156C/en
Priority to PCT/US2001/048569 priority patent/WO2002047797A1/en
Priority to JP2002549362A priority patent/JP2004515349A/en
Publication of CA2329475A1 publication Critical patent/CA2329475A1/en
Priority to US10/851,755 priority patent/US7160367B2/en
Abandoned legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047Pressure swing adsorption
    • B01D53/0476Vacuum pressure swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0407Constructional details of adsorbing systems
    • B01D53/0423Beds in columns
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0407Constructional details of adsorbing systems
    • B01D53/0446Means for feeding or distributing gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047Pressure swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/06Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with moving adsorbents, e.g. rotating beds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/02Preparation of oxygen
    • C01B13/0229Purification or separation processes
    • C01B13/0248Physical processing only
    • C01B13/0259Physical processing only by adsorption on solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/10Inorganic adsorbents
    • B01D2253/104Alumina
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/10Inorganic adsorbents
    • B01D2253/106Silica or silicates
    • B01D2253/108Zeolites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/25Coated, impregnated or composite adsorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/30Physical properties of adsorbents
    • B01D2253/34Specific shapes
    • B01D2253/342Monoliths
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2256/00Main component in the product gas stream after treatment
    • B01D2256/12Oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/10Single element gases other than halogens
    • B01D2257/102Nitrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/10Single element gases other than halogens
    • B01D2257/104Oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/80Water
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40003Methods relating to valve switching
    • B01D2259/40005Methods relating to valve switching using rotary valves
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40077Direction of flow
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40083Regeneration of adsorbents in processes other than pressure or temperature swing adsorption
    • B01D2259/40086Regeneration of adsorbents in processes other than pressure or temperature swing adsorption by using a purge gas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40083Regeneration of adsorbents in processes other than pressure or temperature swing adsorption
    • B01D2259/40088Regeneration of adsorbents in processes other than pressure or temperature swing adsorption by heating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/402Further details for adsorption processes and devices using two beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/403Further details for adsorption processes and devices using three beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/404Further details for adsorption processes and devices using four beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/414Further details for adsorption processes and devices using different types of adsorbents
    • B01D2259/4141Further details for adsorption processes and devices using different types of adsorbents within a single bed
    • B01D2259/4143Further details for adsorption processes and devices using different types of adsorbents within a single bed arranged as a mixture
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0407Constructional details of adsorbing systems
    • B01D53/0431Beds with radial gas flow
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0407Constructional details of adsorbing systems
    • B01D53/0438Cooling or heating systems
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0462Temperature swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047Pressure swing adsorption
    • B01D53/053Pressure swing adsorption with storage or buffer vessel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/26Drying gases or vapours
    • B01D53/261Drying gases or vapours by adsorption
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2210/00Purification or separation of specific gases
    • C01B2210/0043Impurity removed
    • C01B2210/0046Nitrogen
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2210/00Purification or separation of specific gases
    • C01B2210/0043Impurity removed
    • C01B2210/0062Water

Abstract

Disclosed embodiments address contaminant management, particularly water management, challenges that arise during production of desirably contaminant free product fluid in the operation of PSA equipment, particularly challenges that arise under intermittent operation of PSA equipment. One disclosed embodiment of a PSA apparatus includes a breather fluidly coupled to a feed end of an adsorber with a contaminant-sensitive adsorbent.
The breather can be coupled to the feed end through a shutoff valve closed during production and open during shutdown. Other disclosed embodiments of the PSA
apparatus used particular sealing strategies for additional sealing of the apparatus or components thereof. For example, one embodiment comprises a buffer seal for receiving a buffer gas having a contaminant vapor content substantially the same as or less than a product gas produced by a pressure swing adsorption process over the adsorbers. The buffer chamber may have flushing circulation provided by delivered product flow. As a second example of sealing strategy, a parking seal can be used that typically is engaged when the apparatus is parked. Various seals can be used alone, or in combination with other contaminant management features. Embodiments of a method for reducing adsorbent degradation by contaminant adsorption while producing a product gas also are described comprising providing described embodiments of the PSA apparatus or system, and operating such PSA
apparatus or system to produce a product gas. Various embodiments for operating a PSA
apparatus and system during normal product delivery, shutdown, park and start up modes also are described.

Description

Fast Cycle PSA with Adsorbents Sensitive to Atmospheric Humidity FIELD OF THE INVENTION
The invention relates to gas separation by pressure swing adsorption processes operating at high frequency with adsorbents which may be sensitive to deactivation by atmospheric humidity. A particular application is oxygen enrichment of air using nitrogen-selective adsorbents which are hydrophilic in their activated condition.
BACKGROUND OF THE INVENTION
Gas separation by pressure swing adsorption is achieved by coordinated pressure cycling and flow reversals over an adsorber that preferentially adsorbs a more readily adsorbed component relative to a less readily adsorbed component of the mixture. The total pressure is elevated during intervals of flow in a first direction through the adsorber from a first end to a second end of the adsorber, and is reduced during intervals of flow in the reverse direction. As the cycle is repeated, the less readily adsorbed component is concentrated in the first direction, while the more readily adsorbed component is concentrated in the reverse direction.
A "light" product, depleted in the more readily adsorbed component and enriched in the less readily adsorbed component, is then delivered from the second end of the adsorber. A "heavy" product enriched in the more strongly adsorbed component is exhausted from the first end of the adsorber. The light product is usually the desired product to be purified, and the heavy product often a waste product, as in the important examples of oxygen separation over nitrogen-selective zeolite adsorbents and hydrogen purification. The heavy product (enriched in nitrogen as the more readily adsorbed component) is a desired product in the example of nitrogen separation over nitrogen-selective zeolite adsorbents. Typically, the feed is admitted to the first end of a adsorber and the light product is delivered from the second end of the adsorber when the pressure in that adsorber is elevated to a higher working pressure. The heavy product is exhausted from the first end of the adsorber at a lower working pressure. In order to achieve high purity of the light product, a fraction of the light product or gas enriched in the less readily adsorbed component is recycled back to the adsorbers as "light reflux" gas after pressure letdown, e.g. to perform purge, pressure equalization or repressurization steps.
The conventional process for gas separation by pressure swing adsorption uses two or more adsorbers in parallel, with directional valuing at each end of each adsorber to connect the adsorbers in alternating sequence to pressure sources and sinks, thus establishing the changes of working pressure and flow direction.
The basic pressure swing adsorption process also makes inefficient use of applied energy, because of irreversible expansion over the valves while switching the adsorbers between higher and lower pressures. More sophisticated conventional pressure swing adsorption devices achieve some improvement in efficiency by use of multiple pressure equalization steps and other process refinements, but complexity of the valve logic based on conventional 2-way valves is greatly increased. Furthermore, the cycle frequency with conventional valves and granular adsorbent cannot be greatly increased, so the adsorbent inventory is large. Conventional PSA plants are accordingly bulky and heavy, and there is a need for much more compact PSA
technology.
By operating with high surface area laminated adsorbers, with the adsorbent supported in thin sheets separated by spacers to define flow channels between adjacent sheets, and with the adsorbers mounted in a rotor to provide the PSA process valve logic with only one moving part, a high frequency PSA cycle can be performed in an extremely compact apparatus as disclosed by Keefer et al (U.S. Patent No.
6,051,050), the disclosure of which is incorporated herein by reference.
The present invention addresses unexpectedly severe problems with adsorbent deactivation that have been encountered with pressure swing adsorption (PSA) or vacuum pressure swing adsorption (VPSA) gas separation processes using strongly hydrophilic adsorbents and operating at exceptionally high cycle frequency. Such deactivation problems are severe in PSA or VPSA processes working with atmospheric air feed of any normal humidity, and are particularly severe with the highest performance nitrogen-selective adsorbents widely used for oxygen enrichment. Hydrophilic adsorbents such as Li or Ca exchanged low silica X zeolites are extremely sensitive to deactivation by adsorbed water. This problem is most severe in applications with intermittent operation and/or extended shutdowns.
Conventional industrial PSA and VPSA systems operate at low cycle frequency with large inventories of adsorbent, and are relatively insensitive to minor contamination by atmospheric humidity because of ( 1 ) the relatively large dimension of the adsorbers across which humidity diffusion may take place, (2) the slow rate of any deterioration dependant on the cumulative number of cycles experienced, and (3) the relative insensitivity to deactivation of a small fraction of a large adsorbent inventory. Hence, a conventional system may operate for many years with no noticeable degradation.
The inventors have developed advanced PSA or VPSA systems whose operating frequency is some two orders of magnitude faster than conventional industrial PSA processes. Consequently the adsorbent inventory is smaller by approximately the same factor of two orders of magnitude, and the dimension of the adsorbers across which humidity diffusion may take place is also reduced by a large factor.
The inventors have found experimentally that a serious performance decline takes place owing to adsorbent deactivation by water adsorption, within about two months while operating continuously with water saturated air feed at cycle frequencies of the order of 60 cycles/minute, unless the inventive devices and procedures the present invention are applied to prevent such rapid decline.
The performance decline is indicated by a loss of productivity and product yield while operating to maintain delivered oxygen product purity at fixed cycle frequency and within a fixed working pressure range. The tests were conducted using a lithium exchanged low silica X zeolite adsorbent.
The inventors have determined solutions for water management challenges that arise in the operation of fast cycle PSA equipment in normal continuous operation, and have further addressed the more serious challenges that arise under intermittent operation of PSA equipment under diverse climatic conditions of ambient temperature and humidity. When a PSA unit is shutdown, any adsorbed water in any part of the adsorber may diffuse detrimentally into water-sensitive zones of activated adsorbent to cause deactivation. Furthermore, normal fluctuations of ambient temperature and barometric pressure may cause an idled PSA unit to take in humid air through any breather port or through leakage paths in imperfectly closed valves, seals, and compression machinery. Hence, the invention also addresses humidity-safe shutdown procedures, and supplementary devices for excluding or minimizing humidity ingress into a fast cycle PSA
unit when it is in a storage, idled or "parked" condition.
SUMMARY OF THE INVENTION
Aspects of the invention are discussed under the headings of normal operation, shutdown procedures, and parked condition of the PSA unit with water-sensitive adsorbent.
Normal Operation In normal operation of conventional PSA units, water transport from humid feed entering the feed end is prevented by any of the following measures: (1) using a feed air dryer upstream of the PSA unit, (2) using a desiccant layer at the feed end of the adsorbers, and (3) allowing a "sacrificial" layer of the water-sensitive adsorbent adjacent the feed end of the adsorbers to deactivate while functioning effectively as a desiccant.
In preferred embodiments of the present invention, the adsorbers are provided as high surface area laminated adsorbers, with the adsorbent supported in thin adsorbent sheets separated by spacers to define flow channels between adjacent sheets. A desiccant strip is provided at the feed end of the adsorbent sheets, by coating the leading edge of the sheets with a suitable desiccant such as alumina. Alternatively, a narrow ribbon coated with alumina may be placed on the feed side of an adsorbent sheet coated with the water -sensitive adsorbent.
Ideally, we want a desiccant which adsorbs water strongly (so that the strip is short) but with a water isotherm that is reasonably linear (easy regeneration, smallest possible adsorbed water inventory) over the working range. We may want to select an adsorbent with "best" properties for PSA operation, but also "good" properties for thermal swing regeneration to knock out the adsorbed water inventory as a shutdown procedure. The design must determine required width of strip, steady state accumulated adsorbed water profile, effective diffusion rate and ease of regeneration for alternative desiccants.
In order to prevent humidity bypass of the desiccant, it is important to minimize leakage past laminate packs, static seals, and any gross channeling.
Static seal configurations and compounds must be selected for low water permeation flux.
Water leakage into product valve and lines must stringently be avoided since humidity contaminating the product end of the adsorbers will work backwards under operation of the PSA process to degrade the entire adsorbent inventory eventually. The object is to prevent water ingress into the product end of the adsorbers from all pathways. Hence, careful precautions must be taken to minimize boundary layer back-diffusion and surface diffusion from downstream product lines, valves and receivers; and to have absolutely tight shut-off valves to close the product delivery line when the unit is shut down.
The directional control valves that execute the PSA cycle at the product ends of the adsorbers (here, preferably rotary multiport distributor valves) must be designed so that leakage of humid air into these valves and thence into the adsorbers is strictly avoided. Such leakage is more likely when the PSA beds are vacuum regenerated as in normal practice. Humidity leakage prevention is especially difficult for the circumferential seals of relatively large diameter rotary multiport distributor valves, although actuator packings of any type of directional valve will also provide potential leakage pathways for humidity ingress. The approach provided within the present invention is to provide a buffer space between the internal working zone of valves communicating to the product ends of the adsorbers. The buffer space is a positive pressured dry oxygen flushed zone, with flushing circulation conveniently by delivered product flow. For rotary multiport distributor valves, the buffer space is defined by a buffer seal, preferably of much smaller diameter than the circumferential seals or sealing face of the rotary valve.
The invention provides desiccant traps in all light reflux lines (and the buffer space of any directional valve) to capture any mobile water, particularly upon initial startup or upon startup after any maintenance intervention which may have introduced humid air into the PSA unit. The activity of such desiccant traps may be maintained by periodic regeneration or replacement. The desiccant traps in light reflux lines may serve usefully as surge absorber chambers or equalization buffer tanks. These desiccant traps may be static (with periodic replacement or reactivation if needed during scheduled maintenance). The chosen desiccant should be strong, e.g. perhaps used nitrogen-selective adsorbent.
If one of these desiccant traps is in the product line, its steady state humidity level corresponds to that of the dry delivered product. If a previously water loaded desiccant trap is valued into the product line, it will be gradually regenerated to a high degree by displacement purge of product gas. An auxiliary valuing arrangement may be used to rotate desiccant traps between the light reflux lines and the product line, for displacement purged regeneration by the product.
The dry product may also be used to regenerate any auxiliary beds used as (1) a humidity sink for regenerating desiccant at the front end of the adsorbers, or (2) isolation desiccant traps for air breather lines when the unit is in shutdown mode.

Shutdown Procedures Forward diffusion of water from previously adsorbed in the feed end desiccant strip of the adsorbers is a serious hazard for progressive deactivation of the water-sensitive adsorbent whenever the PSA unit is shut down. Alternative approaches within the invention include (1) isolation valves, (2) back purge with dry product, (3) back purge with auxiliary heating of the desiccant strip, and (4) recirculated back purge to transfer humidity from the desiccant strip to an auxiliary desiccant bed.
Isolation valves may be provided between desiccant and the water-sensitive adsorbent zones in each adsorber. These valves are open whenever the unit is operating, but are closed automatically whenever the unit stops. The isolation valves may be normally closed, and then opened either by admission of feed pressurized above ambient or by rotation of the rotary PSA module of preferred embodiments. The isolation valves must close tightly to withstand pressure fluctuations due to ambient temperature variations, to avoid forcing ambient humidity ingress into the adsorbers.
Particularly preferred strategies entail regeneration of the desiccant strip to eliminate most of the adsorbed water in the desiccant. With high concentrations of adsorbed water, water diffuses relatively rapidly because the slope of the water isotherm is less steep. When nearly all of the water has been removed by successful regeneration, water diffuses much more slowly because the slope of the water isotherm is extremely steep. Hence, the rate of deactivation of our water-sensitive adsorbent can be greatly reduced by nearly complete regeneration of the desiccant; and a substantial improvement can be obtained by only partial regeneration of the desiccant to remove the excess water which has greatest diffusive mobility.

Initial desiccant regeneration can be achieved by an automatic back purge with stored dry oxygen product upon shutdown. To ensure equal regeneration of the desiccant strip in all adsorbers, it is important to keep the rotor turning during purge. As a very large volume of stored dry product would be required to achieve substantially complete regeneration of the desiccant strip, the effectiveness of regeneration may be enhanced by back purging with the assistance of the operating vacuum pump.
A greater enhancement of desiccant regeneration may be achieved by auxiliary heating of the desiccant strip during the shutdown procedure and while back purging is underway with or without vaccum assist. Alternative heat sources auxiliary resistance heaters, inductive eddy current heating (e.g. of a metallic mesh or foil in the adsorbent sheets) or microwave radiation. Alternatively, heat may be provided to the desiccant strip by deliberately increased heating (or reduced normal cooling) by the vacuum pump and compressor operating with recirculating gas flows, or by rotary valve seal friction which may be increased by increasing valve face mechanical loading.
Even with vacuum assist and auxiliary heating of the desiccant strip, the volume of dry product required for back purging may be unreasonably large.
Hence, another aspect of the invention is to extend back purge by using the vacuum pump for recirculated purge by product gas through an auxiliary desiccant/adsorbent bed, which will be regenerated in normal operation by dry product flow through that adsorbent bed and/or by thermal swing heating.
Again, the shutdown procedure must be designed to place the PSA unit in a humidity-safe parked condition under which water leakage into the product end of the adsorbers is strictly prevented by appropriate tightly closed shut-off valves and/or non-return valves. Water ingress into the product ends of the adsorbers must be stopped from any and all pathways. Tight sealing of buffer seals around circumferential rotary valve seals or valve actuator stems may be augmented by automatically engaged parking seal(s). During normal operation of a rotary PSA

embodiment, the buffer seal should be designed for low friction and long life.
Its sealing tightness during operation may be non-critical since the buffer chamber is then positively pressurized above ambient pressure. Sealing tightness does become critical during shutdown, as any direct "breathing" of humid ambient air into the product ends of the adsorbers must be strictly prevented. The buffer seal may therefore be supplemented by a "parking seal" , which enters a tightly closed engagement automatically when either (1) rotation of a rotary PSA module is discontinued, or alternatively when (2) the PSA unit is unpressurized owing to discontinuation of compressed feed gas supply.
Parked Condition As described above, a proper shutdown procedure will have protected the water-sensitive adsorbent zones from deactivation, either by engaging isolation valves to isolate the water containing desiccant strip, or else by regenerating the desiccant strip.
When the PSA unit has been shutdown, it is externally exposed to humid air, and it is subjected to normal fluctuations of diurnal temperature and barometric pressure. As indicated above, it is mandatory that water transport from humid air breathing in and out of the product end of the PSA unit be substantially completely excluded. The invention next addresses the issue of preventing or managing humid air breathing in and out of the feed end of the PSA
unit.
In one aspect of the invention with several embodiments, the water-sensitive zone of the PSA unit is totally or at least partially sealed on shutdown.
In a completely sealed shutdown, the PSA unit (or its water-sensitive zone) is tightly sealed on all ports after shutdown. As the unit cools from its normal operating temperature (here assumed to be somewhat above normal ambient temperature), it pulls a strong vacuum which may be further enhanced while adsorbed nitrogen redistributes by diffusion. A relief valve is provided to vent any excess air if the pressure starts cycling up to higher pressures as a result of any slow leakage inward, or as a result of inadvertent heating of the unit.
Similarly, a relief valve may be provided to permit a modest inflow of air to the feed end of the PSA unit as may be required to relieve excessive differential pressure between external ambient pressure and the internal vacuum pressure.
In another aspect of the invention, the PSA unit is tightly sealed on all product end ports and seals, but is only partially sealed sealed on feed ports so as to allow restricted breathing in response to changes of ambient temperature and barometric pressure. Crossover relief valves with a low cracking pressure setting may be provided to permit limited feed end breathing only as required to prevent excessive over-pressure or vacuum differentials that would overload the unit structurally or cause some risk that breathing of humid air into the product end may take place despite all precautions. Any breathing of external air into the feed end of the PSA unit would be through the desiccant strip at the feed end of adsorbers. An extra air breather desiccant bed may be provided on an air breather port communicating to the feed end of the PSA unit.
A further refinement of the invention is thermal design of air breather and air breather desiccant bed in conjunction with the PSA module, so that ambient temperature swings penetrate the desiccant bed associated with the air breather very rapidly and penetrate the the PSA module more slowly. Hence a phase shift is established between temperature swings in the air breather desiccant bed and air flows through that desiccant bed, as those air flows will be in phase with the rate of delayed temperature change within the adsorbers of the PSA unit. Air flow into the PSA unit occurs as it is cooling down, after the air breather desiccant bed has already cooled down so as to adsorb humidity more strongly. Air flow out of the PSA unit occurs as it is warming up, after the air breather desiccant bed has already warmed up so as to release adsorbed water vapour.
Consequently a thermal swing adsorption (TSA) process is established in the air breather desiccant bed, operative to slowly expel water out of the PSA
unit on a 24 hour nominal cycle. This auxiliary TSA humidity expulsion process could have passive solar augmentation for extra thermal swing. The air breather desiccant bed may be designed with a large volume and a long flow path to minimize the rate of nitrogen mixing into oxygen within the adsorbers.
Another aspect of the invention more simply is to provide the air breather as a long tube (with or without desiccant) to retard bulk mixing of humid external air with dry oxygen in the adsorbers. Otherwise, air breathing will result in nitrogen uptake with a net inward flow of several bed volumes into the adsorbers, plus pumping of feed end humidity.
Tests of this embodiment have established that the rate of adsorbent deactivation under air breathing (as forced by cyclic ambient temperature variations) is greatly retarded by an air breather tube whose internal volume may be much less than the adsorber volume.
Yet another aspect of the invention is to provide an air breather as an inflated bag diaphragm approximately equilibriated with ambient pressure, to prevent bulk mixing of humid external air with dry oxygen within the adsorbers.
As mentioned above, water ingress during shutdown may be prevented by tight shut-off valves or non-return valves in downstream product lines, and by parking seals around circumferential dynamic seals of rotary valves and any valve actuator stems. Parking seals should be extremely tight, and on a small diameter by good mechanical design. Desiccant traps in light reflux lines and valve buffer spaces can capture any mobile water, with periodic regeneration or replacement of those desiccant traps being included in normal PSA unit maintenance procedures..
It is important to avoid non-uniform adsorber degradation owing to parked position of valve ports singling out particular adsorbers to get different shutdown circulation patterns and humidity exposure. This risk ma be addressed by any of the following measures:

(1) remove water very stringently upon shutdown, and then seal tightly, (2) periodically turn rotor during shutdown, or (3) lift valve faces) off seat during shutdown so that all adsorbers are vented together.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 shows an axial section of a rotary PSA module.
Figs. 2 through SB show transverse sections of the module of Fig. 1.
Figs. 6 through 15 show a simplified and generalized schematic of fast cycle PSA modules with devices for preventing or inhibiting deactivation of the water-sensitive adsorbent zone.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Figs. 1 - 5 Fig. 1 shows a rotary PSA module 1, particularly suitable for smaller scale oxygen generation. Module 1 includes a number "N" of adsorbers 3 in adsorber housing body 4.
Each adsorber has a first end 5 and a second end 6, with a flow path therebetween contacting a nitrogen-selective adsorbent. Each adsorber has a first zone 3A adjacent its first end, and a second zone 3B extending to the second end.
First zone 3A contains a desiccant such as activated alumina or a zeolite adsorbent, and second zone 3B contains a water-sensitive nitrogen-selective adsorbent as further described below. Typically, zone 3A extends over about 15 %
of the adsorber length between the first and second ends, and zone 3B (which may in turn be subdivided into a plurality of zones containing different adsorbents) is the remaining 85 % . The adsorbers are deployed in an axisymmetric array about axis 7 of the adsorber housing body. The housing body 4 is in relative rotary motion about axis 7 with first and second valve bodies 8 and 9, housing body 4 being engaged across a first valve face 10 with the first valve body 8 to which feed air is supplied and from which nitrogen-enriched air is withdrawn as the heavy product, and housing body 4 being engaged across a second valve face 11 with the second valve body 9 from which oxygen-enriched air is withdrawn as the light product.
In some embodiments (not shown), the adsorber housing body may be stationary, while the first and second valve bodies rotate. In those preferred embodiments as particularly depicted in Figs. 1 - 5, the adsorber housing 4 rotates and shall henceforth be referred to as the adsorber rotor 4, while the first and second valve bodies are stationary and together constitute a stator assembly 12 of the module. The first valve body shall henceforth be referred to as the first valve stator 8, and the second valve body shall henceforth be referred to as the second valve stator 9.
In the embodiment shown in Figs. 1 - 5, the flow path through the adsorbers is parallel to axis 7, so that the flow direction is axial, while the first and second valve faces are shown as flat annular discs normal to axis 7.
However, more generally the flow direction in the adsorbers may be axial or radial, and the first and second valve faces may be any figure of revolution centred on axis 7. The steps of the process and the functional compartments to be defined will be in the same angular relationship regardless of a radial or axial flow direction in the adsorbers.
Figs. 2 - 5 are cross sections of module 1 in the planes defined by arrows 12 - 13, 14 - 15, and 16 - 17. Arrow 20 in each section shows the direction of rotation of the rotor 4.
Fig. 2 shows section 12 - 13 across Fig. l , which crosses the adsorber rotor. Here, "N" = 72. The adsorbers 3 are mounted between outer wall 21 and inner wall 22 of adsorber wheel 208. Each adsorber comprises a rectangular flat pack 3 of adsorbent sheets 23, with spacers 24 between the sheets to define flow channels here in the axial direction. Separators 25 are provided between the adsorbers to fill void space and prevent leakage between the adsorbers.
The adsorbent sheets comprise a reinforcement material, in preferred embodiments glass fibre, metal foil or wire mesh, to which the adsorbent material is attached with a suitable binder. For air separation to produce enriched oxygen, typical adsorbents in second zone 3B are X, A or chabazite type zeolites, typically exchanged with lithium, calcium, strontium, magnesium and/or other canons, and with optimized silicon/aluminum ratios as well known in the art. The zeolite crystals are bound with silica, clay and other binders, or self-bound, within the adsorbent sheet matrix.
Satisfactory adsorbent sheets have been made by coating a slurry of zeolite crystals with binder constituents onto the reinforcement material, with successful examples including nonwoven fibreglass scrims, woven metal fabrics, and expanded aluminum foils. Spacers are provided by printing or embossing the adsorbent sheet with a raised pattern, or by placing a fabricated spacer between adjacent pairs of adsorbent sheets. Alternative satisfactory spacers have been provided as woven metal screens, non-woven fibreglass scrims, and metal foils with etched flow channels in a photolithographic pattern.
Typical experimental sheet thicknesses have been 150 microns, with spacer heights in the range of 100 to 150 microns, and adsorber flow channel length approximately 20 cm. Using X type zeolites, excellent performance has been achieved in oxygen separation from air at PSA cycle frequencies in the range of 30 to 150 cycles per minute.
Fig. 3 shows the porting of rotor 4 in the first and second valve faces respectively in the planes defined by arrows 14 - 15, and 16 - 17. An adsorber port 30 provides fluid communication directly from the first or second end of each adsorber to respectively the first or second valve face.

Fig. 4 shows the first stator valve face 100 of the first stator 8 in the first valve face 10, in the plane defined by arrows 14 - 15. Fluid connections are shown to a feed compressor 101 inducting feed air from inlet filter 102, and to an exhauster 103 delivering nitrogen-enriched second product to a second product delivery conduit 104. Compressor 101 and exhauster 103 are shown coupled to a drive motor 105.
Arrow 20 indicates the direction of rotation by the adsorber rotor. In the annular valve face between circumferential seals 106 and 107, the open area of first stator valve face 100 ported to the feed and exhaust compartments is indicated by clear angular segments 111 - 116 corresponding to the first functional ports communicating directly to functional compartments identified by the same reference numerals 111 - 116. The substantially closed area of valve face 100 between functional compartments is indicated by hatched sectors 118 and 119 which are slippers with zero clearance, or preferably a narrow clearance to reduce friction and wear without excessive leakage. Typical closed sector 118 provides a transition for an adsorber, between being open to compartment 114 and open to compartment 115.
Gradual opening is provided by a tapering clearance channel between the slipper and the sealing face, so as to achieve gentle pressure equalization of an adsorber being opened to a new compartment. Much wider closed sectors (e.g. 119) are provided to substantially close flow to or from one end of the adsorbers when pressurization or blowdown is being performed from the other end.
The feed compressor provides feed air to feed pressurization compartments 111 and 112, and to feed production compartment 113. Compartments 111 and 112 have succcessively increasing working pressures, while compartment 113 is at the higher working pressure of the PSA cycle. Compressor 101 may thus be a multistage or split stream compressor system delivering the appropriate volume of feed flow to each compartment so as to achieve the pressurization of adsorbers through the intermediate pressure levels of compartments 111 and 112, and then the final pressurization and production through compartment 113. A split stream compressor system may be provided in series as a multistage compressor with interstage delivery ports; or as a plurality of compressors or compression cylinders in parallel, each delivering feed air to the working pressure of a compartment 111 to 113. Alternatively, compressor 101 may deliver all the feed air to the higher pressure, with throttling of some of that air to supply feed pressurization compartments 111 and 112 at their respective intermediate pressures.
Similar, exhauster 103 exhausts nitrogen-enriched heavy product gas from countercurrent blowdown compartments 114 and 115 at the successively decreasing working pressures of those compartments, and finally from exhaust compartment which is at the lower pressure of the cycle. Similarly to compressor 101, exhauster 103 may be provided as a multistage or split stream machine, with stages in series or in parallel to accept each flow at the appropriate intermediate pressure descending to the lower pressure.
In the example embodiment of Fig. 4A, the lower pressure is ambient pressure, so exhaust compartment 116 exhaust directly to heavy product delivery conduit 104. Exhauster 103 thus provides pressure letdown with energy recovery to assist motor 105 from the countercurrrent blowdown compartments 114 and 115.
For simplicity, exhauster 103 may be replaced by throttling orifices as countercurrent blowdown pressure letdown means from compartments 114 and 115.
In some preferred embodiments, the lower pressure of the PSA cycle is subatmospheric. Exhauster 103 is then provided as a vacuum pump, as shown in Fig.
4B. Again, the vacuum pump may be multistage or split stream, with separate stages in series or in parallel, to accept countercurrent blowdown streams exiting their compartments at working pressures greater than the lower pressure which is the deepest vacuum pressure. In Fig. 4B, the early countercurrent blowdown stream from compartment 114 is released at ambient pressure directly to heavy product delivery conduit 104. If for simplicity a single stage vacuum pump were used, the countercurrent blowdown stream from compartment 115 would be throttled down to the lower pressure over an orifice to join the stream from compartment 116 at the inlet of the vacuum pump.

Figs. 5A and SB shows the second stator valve face, at section 16 - 17 of Fig.
1. Open ports of the valve face are second valve function ports communicating directly to a light product delivery compartment 121; a number of light reflux exit compartments 122, 123, 124 and 125; and the same number of light reflux return compartments 126, 127, 128 and 129 within the second stator. The second valve function ports are in the annular ring defined by circumferential seals 131 and 132.
Each pair of light reflux exit and return compartments provides a stage of light reflux pressure letdown, respectively for the PSA process functions of supply to backfill, full or partial pressure equalization, and cocurrent blowdown to purge.
Illustrating the option of light reflux pressure letdown with energy recovery, a split stream light reflux expander 140 is provided to provide pressure let-down of four light reflux stages with energy recovery. The light reflux expander serves as pressure let-down means for each of four light reflux stages, each stage having a light reflux loop conduit 134 respectively between light reflux exit and return compartments 122 and 129, 123 and 128, 124 and 127, and 125 and 126 as illustrated. Desiccant traps (auxiliary desiccant beds) 135 and 136 are respectively installed within the light product delivery conduit 147 and each light reflux loop conduit 134.
Light reflux expander 140 is coupled to a light product pressure booster compressor 145 by drive shaft 146. Compressor 145 receives the light product from conduit 25, and delivers light product (compressed to a delivery pressure above the higher pressure of the PSA cycle) to delivery conduit 147. Since the light reflux and light product are both enriched oxygen streams of approximately the same purity, expander 140 and light product compressor 145 may be hermetically enclosed in a single housing which may conveniently be integrated with the second stator as shown in Fig. 1. This configuration of a "turbocompressor" oxygen booster without a separate drive motor is advantageous, as a useful pressure boost of the product oxygen can be achieved without an external motor and corresponding shaft seals, and can also be very compact when designed to operate at very high shaft speeds.

Fig. 5B shows the simpler alternative of using a throttle orifice 150 as the pressure letdown means for each of the light reflux stages.
Turning back to Fig. 1, compressed feed air is supplied to compartment 113 as indicated by arrow 125, while nitrogen enriched heavy product is exhausted from compartment 117 as indicated by arrow 126. The rotor is supported by bearing with shaft seal 161 on rotor drive shaft 162 in the first stator 8, which is integrally assembled with the first and second valve stators. The adsorber rotor is driven by motor 163 as rotor drive means.
As leakage across outer circumferential seal 131 on the second valve face 11 may compromise enriched oxygen purity, and more importantly may allow ingress of atmospheric humidity into the second ends of the adsorbers which could deactivate the nitrogen-selective adsorbent, a buffer seal 170 is provided to provide more positive sealing of a buffer chamber 171 between seals 131 and 171. Even though the working pressure in some zones of the second valve face may be subatmospheric (in the case that a vacuum pump is used as exhauster 103), buffer chamber is filled with dry enriched oxygen product at a buffer pressure positively above ambient pressure. Hence, minor leakage of dry oxygen outward may take place, but humid air may not leak into the buffer chamber. In order to further minimize leakage and to reduce seal frictional torque, buffer seal 171 seals on a sealing face 172 at a much smaller diameter than the diameter of circumferential seal 131. Buffer seal 170 seals between a rotor extension 175 of adsorber rotor 4 and the sealing face 172 on the second valve stator 9, with rotor extension 175 enveloping the rear portion of second valve stator 9 to form buffer chamber 171. The buffer seal may be designed to have relatively light engagement for low friction and wear while the PSA unit is under normal operating conditions of rotation and pressurization, and then to engage tightly on its sealing face as a "parking" seal when the PSA unit is shut down. The parking seal may also be provided as a separate sealing element cooperating with buffer seal 171, and engaged only during shut down.

Product oxygen from light product functional compartment 121 is delivered by channel 176 into buffer chamber 171, and after circulation through chamber is delivered by conduit 177 to product booster compressor 145 or else directly to product delivery conduit 147. A stator housing member 180 is provided as structural connection between first valve stator 8 and second valve stator 9.
Figs. 6 - 15 In the following figures of this disclosure, simplified schematics will represent the PSA apparatus as described above. These highly simplified drawings will indicate just a single feed conduit 181 to, and a single heavy product conduit 182 from, the first valve face 10; and the light product delivery conduit 147 and a single representative light reflux stage 184 with pressure let-down means communicating to the second valve face 11. Figures 6 - 15 may be taken to include PSA
embodiments with rotary adsorbers, PSA embodiments with rotary distributor valves and stationary adsorbers, and for greatest generality other PSA devices with any type of directional valve mechanism and any number of stationary or moving adsorbers.
The adsorbers 3 are contained within an adsorber compartment 200 (shown by dashed lines in Figs. 6 - 15) whose thermal regime is important in some of the embodiments disclosed hereunder. Adsorber compartment 200 may also enclose some or all of the PSA process valuing and process logic. Compartment 200 may be simply an area under a given thermal regime isolated from the external ambient to some extent, or it may be physically contained to provide isolation from the external humid atmosphere as a general approach to protect the PSA system against water vapour ingress by any pathway.
The following embodiments provide solutions for humidity management with water-sensitive adsorbents under normal operation, shutdown procedures and parked condition of the PSA unit. While the discussion will focus on the important application to oxygen enrichment over nitrogen-selective adsorbents which are especially water-sensitive, it will be appreciated that the features of the invention are broadly applicable to any PSA device and process for separating any gas mixture (or purifying any gas component) over adsorbent which may be deactivated or otherwise degraded by contact with atmospheric humidity for air either introduced within the PSA unit as part of its process duty, or else just externally contacting the PSA unit.
Fig 6 shows a non-return valve 201 and a shutoff valve 202 deployed in series in product delivery conduit 147, so as to positively prevent back-migration of water from the product receiver or consumer when the PSA unit is shut down.
Fig. 6 further shows a light product storage vessel or surge chamber 203, which communicates with conduit 147 and which provides a volume of dry light product gas as shutdown purge gas for partial regeneration of the desiccant adsorber zone 3A upon depressurization and shutdown of the PSA unit. It is most desirable to keep the rotor or rotary valve turning during purge, so all adsorbers are purged equally. Vacuum pump 103 may be operated so as to increase the degree of regeneration of desiccant zone 3A that can be achieved with a finite volume of purge gas from receiver 203.
Fig. 6 also shows a auxiliary heater device 210 which is used to heat the desiccant adsorber zone 3A for enhanced regeneration during shutdown purging from surge chamber 203. Heater device 210 may generally use any technique for localized heating. Alternative suitable heater devices may be based on electrical resistance heaters embedded on adsorber zone 3A, or on infrared heat lamp radiation ntios, or microwave radiation. As some preferred embodiments of the adsorbent laminate use wire mesh screens or metal foils as the adsorbent sheet support, inductive eddy current heating is also a viable heater device approach within the invention. Localized heating may also achieved by increasing the load on rotary valve seals, or by operating the vacuum pump and/or compressor in a recirculation mode so as to heat at least the feed end of the adsorbers.

Fig. 7 shows an embodiment for extended back purge of the desiccant, by using the vacuum pump 103 for recirculated purge (preferably by oxygen-enriched air) through an auxiliary desiccant/adsorbent bed 210, which will be regenerated in subsequent normal operation by dry product and/or thermal swing. The operating principle of this embodiment is to achieve substantially complete regeneration of desiccant zone 3A, by displacement purge to transfer the adsorbed water vapour form zone 3A to auxiliary desiccant bed 210. Desiccant bed 210 must be large enough in water vapour capacity to adsorb substantially all the water vapour desorbed from zone 3A, without any breakthrough of water vapour that would contaminate the water-sensitive adsorber zones 3B from the product end.
Auxiliary directional valves 211, 212 and 213 are provided to enable the shutdown regeneration procedure. During normal operation, valve 210 is open, and valves 211 and 212 are closed, so that the vacuum pump discharges to atmosphere, while the dry oxygen-enriched product gas passes countercurrently through auxiliary desiccant bed 210 to regenerate it. During the shutdown regeneration procedure, valve 210 is closed while valves 211 and 212 are open so that the vaccum pump recirculates purge gas via valve 211 cocurrently through auxiliary desiccant bed 210 and then through valve 212 back to purge adsorbers 3 countercurrently from the product end. A humidity sensor 215 may be provided as a safety device to warn of any water vapour breakthrough that could contaminate the water-sensitive adsorber zones 3B, and desirably to trigger an automatic shutdown by closing valve 212 and stopping vacuum pump 103.
Figs. 8 - 10 show isolation valves 220 between the desiccant and water-sensitive adsorber zones 3A and 3B. These valves along with light end parking seal must be absolutely tight and capable of withstanding maximum pressures due to temperature variations, otherwise we will be forcing ambient humidity ingress into adsorbers. Fig. 8 shows a two-way valve 220 between zones 3A and 3B of each adsorber, with valve 220 to be closed whenever the PSA unit is stopped.
Valve 220 may be normally closed, and opened by rotation of a rotary PSA
module or alternatively opened by generation of positive pressure from compressor 101. Fig. 9 shows each valve 220 as a check valve which prevents forward flow from zone 3A to zone 3B of each adsorber, except during normal intentional operation of the PSA module when check valve 220 is unseated by actuator 225, in turn energized by valve rotation or by compressor pressurization.
Fig. 10 shows the concept of isolation valves carrried to the extreme of separating the PSA module into two stages with isolation valves 220 between the stages to be closed during shutdown. Here, the second stage is a PSA module with first valves 10' and second valves 11 cooperating with adsorbers 3A which contain water-sensitive adsorbent.
The first stage is a pretreatment desiccant dryer module which may operate on a PSA cycle (at the same or a different cyclic frequency as the second stage PSA
module) or alternatively could operate on a thermal swing adsorption (TSA) cycle. The first stage module has first valves 10 and second valves 11' cooperating with desiccant adsorbers 3A.
It will be evident that the water-sensitive adsorber zones 3B in each of the embodiments in Figs. 8 - 10 must be isolated from the atmosphere during shutdown to prevent water vapour ingress. If the PSA module (or the portion thereof containing adsorber zones 3B) is tightly sealed on all ports after shutdown, it will typically go into a vacuum condition as it cools from operating temperature and as adsorbed nitrogen (or other adsorbate) redistributes by diffusion within the adsorbers. If the PSA module has been shutdown and sealed during cold weather, its internal pressure may however rise well above atmospheric during hot weather.
Unless the PSA module is fully or partially vented to atmosphere, its internal pressure will cycle in response to diurnal and seasonal temperature variations. An externally venting relief valve is preferably provided to vent any excess air and thus avoid excessive internal pressures if the pressure starts cycling up to higher pressures as a result of slow leakage inward. An internally venting relief valve may also be provided to relieve any excessively deep internal vacuum resulting from cool-down during cold weather.

Figs. 11 - 13 show air breather devices to allow approximate pressure equilibriation between the external environment and the internal working spaces of the PSA unit. By avoiding large pressure differentials, the risk of humidity ingress into the product ends of the adsorbers is reduced. Therefore, the air breather device preferably communicates to the feed end of the adsorbers.
Successful air breather devices will inhibit penetration of atmospheric water vapour into the adsorbers. The object is to reduce or eliminate water transport from humid air breathing in and out of the feed end due to fluctuations of diurnal temperature and barometric pressure.
Fig. 11 shows an air breather provided as a long tube 230 without desiccant to retard bulk mixing of humid external air with dry oxygen in the adsorbers. Air breather 230 may be connected via shutoff valve 231 to adjacent the feed end of all the adsorbers in parallel. Valve 231 is closed during normal operation, but open during shutdown. If desired, valve 231 may be intentionally be undersized to severely restrict gas flows through breather 230. Tests of this embodiment have established that the rate of adsorbent deactivation under air breathing (as forced by cyclic ambient temperature variations) is greatly retarded by an air breather tube whose internal volume may be much less than the adsorber volume.
Fig. 12 shows an air breather provided as an inflated bag diaphragm 235 again communicating to the feed end of the adsorbers through shutoff valve 231.
Diaphragm 235 enables approximate equilibration of the internal working space of the adsorbers with ambient pressure, but substantially prevents bulk mixing of humid external air with dry oxygen within the adsorbers.
Fig. 12 also shows a partly sealed shutdown. The PSA module is tightly sealed on oxygen ports, and fairly tightly sealed on feed ports. Crossover relief valves with a low cracking pressure setting are provided to permit limited feed end breathing only as required to prevent excessive pressure or vacuum build-up.
Relief valve 240 enables external venting to relief over-pressure, and relief valve 241 enables internal venting to prevent excessive internal vacuum that could exceed structural limitations or at least increase the risk of water vapour ingress through minor leakage pathways into the product end of the adsorbers.
Fig. 13 shows an air breather with an auxiliary desiccant bed 250 deployed in air breather 230 and externally to the PSA module which itself is in a zone or compartment 200 having relatively less thermal contact to the external environment (or much greater thermal inertia) than the auxiliary desiccant bed, so that ambient temperature swings penetrate the desiccant bed 250 associated with the air breather very rapidly and penetrate the PSA module more slowly. Desiccant bed 250 may be wrapped around a portion of compartment 200, or may even be arranged to be heated by ambient solar radiation that will then cause a fast temperature rise of desiccant bed 250 and much slower temperature rise within compartment 200, following by faster cooling of bed 250 compared to compartment 200.
Hence a phase shift is established between temperature swings in the air breather desiccant bed and air flows through that desiccant bed, as those air flows will be in phase with the rate of delayed temperature change within the adsorbers of the PSA unit. Air flow into the PSA unit occurs as it is cooling down, after the air breather desiccant bed has already cooled down so as to adsorb humidity more strongly. Air flow out of the PSA unit occurs as it is warming up, after the air breather desiccant bed has already warmed up so as to release adsorbed water vapour.
Consequently a thermal swing adsorption (TSA) process is established in the air breather desiccant bed, operative to slowly expel water out of the PSA
unit on a 24 hour nominal cycle. This auxiliary TSA humidity expulsion process could have passive solar augmentation for extra thermal swing of bed 250. The air breather desiccant bed may be designed with a large volume and a long flow path to minimize the rate of nitrogen mixing into oxygen within the adsorbers.

Similar to Figs. 5A and SB, Fig. 14 shows an auxiliary desiccant bed 135 in product line 147 and another auxiliary desiccant bed 136 in the light reflux loop 184. Fig. 15 also shows auxiliary desiccant beds 135 and 136 deployed as humidity traps in product line 147 and light reflux loop 184, with the further feature of directional valve logic to allow periodic rotation of the desiccant beds between the light reflux lines where water may accumulate or else be returned eventually back into the product ends of the adsorbers, and into the product line where continuous regeneration by dry product takes place once initial dehumidification has taken place after startup.
As shown in Fig. 15, an auxiliary directional valuing arrangement may be used to rotate desiccant traps between the light reflux lines and the product line, for displacement purged regeneration by the product. A plurality of desiccant beds (e.g. 135 and 136) are mounted within a rotary adsorption module 160 having a first rotary valve 161 and a second rotary valve 162 with rotary axis 163.
Rotary adsorption module 160 may rotated continuously at very low rotary speed, or preferably may be rotated through discrete fractional rotations at discrete intervals to switch the desiccant beds from humidity adsorption from each of several light reflux loops to the regeneration position when connected into the product line 147. Regeneration of a desiccant bed connected into product line may be assisted by an auxiliary heater (e.g. a heat lamp) in that position, as water displaced during regeneration will be removed by the product gas and will then not be recirculated into the product ends of the water-sensitive adsorber zones 3B.
The normally extremely dry product gas (optionally assisted by auxiliary heaters) may also be used to regenerate any auxiliary desiccant beds used as (1) a humidity sink for regenerating desiccant at the front end of the adsorbers, or (2) isolation desiccant traps for air breather lines when the unit is in shutdown mode.
The product may also be used to regenerate any auxiliary beds used as ( 1 ) a humidity sink for regenerating desiccant at the front end of the adsorbers, or (2) isolation desiccant traps for air breather lines when the unit is in shutdown mode.

Claims (119)

1. A PSA apparatus, comprising adsorbers with contaminant-sensitive adsorbents having a feed end fluidly coupled to a breather through a shutoff valve closed during production and open during shutdown.
2. The apparatus according to claim 1 where the PSA apparatus is a fast cycle apparatus.
3. The apparatus according to claim 2 where the PSA apparatus operates at a cycle frequency of at least 30 cycles per minute.
4. The apparatus according to claim 3 further comprising a buffer chamber.
5. The PSA apparatus according to claim 1 where the contaminant is water.
6. The apparatus according to claim 1 where the breather includes a contaminant adsorbent material.
7. The apparatus according to claim 6 where the breather includes a desiccant material.
8. The apparatus according to claim 1 where the adsorbers comprise a first material for adsorbing the contaminant and a second adsorbent material for product purification.
9. The apparatus according to claim 8 where the contaminant is water and the first material comprises a desiccant.
10. The apparatus according to claim 9 where the first material comprises a mixture of materials.
11. The apparatus according to claim 1 where the adsorber is a laminate.
12. The apparatus according to claim 8 where the desiccant is in a first zone and the second adsorbent material is in a second zone along a feed direction.
13. The apparatus according to claim 12 the first zone being isolated on shutdown from an adsorbent zone having an adsorbent sensitive to water by a shut off valve in line between the first zone and the adsorbent zone.
14. The apparatus according to claim 13 where the desiccant is housed in a first module separate from but fluidly coupled to a second module housing the adsorbent through a shut off valve in a fluid conduit coupling the first module and the second module.
15. The apparatus according to claim 1 further having a product delivery compartment that receives a buffer gas having a water vapor content substantially the same as or less than the product.
16. The apparatus according to claim 15 where the buffer gas is a product gas produced by pressure swing adsorption over the adsorbers.
17. The apparatus according to claim 1 comprising a rotary PSA apparatus.
18. A PSA apparatus comprising adsorbers having contaminant-sensitive adsorbents with a product end fluidly coupled to a buffer chamber that receives a flowing buffer gas having a contaminant content substantially the same as or less than a product gas purified by a pressure swing adsorption process over the adsorbers.
19. The apparatus of claim 18 where the adsorbers comprise water-sensitive adsorbents and the buffer gas has a water content substantially the same as or less than the product gas.
20. The apparatus according to claim 18 where the buffer gas pressurizes the product delivery compartment to a pressure above ambient.
21. The apparatus according to claim 18 operating at a cycle frequency of at least 30 cycles per minute.
22. The apparatus according to claim 18 where the buffer gas is the product gas.
23. The apparatus according to claim 18 further comprising at least a buffer chamber seal to substantially fluidly seal the buffer chamber.
24. The apparatus according to claim 18 where a feed end of the adsorbers is fluidly coupled to a breather.
25. The apparatus according to claim 24 where the breather includes a contaminant-adsorbent material.
26. The apparatus according to claim 25 where the contaminant adsorbent material includes a desiccant material.
27. The apparatus according to claim 24 and further including an isolation valve in a feed gas path between the breather and the adsorbers.
28. The apparatus according to claim 18 where the adsorbers comprise laminates having a first material for adsorbing contaminant and a second material for separating a product gas from a gas mixture.
29. The apparatus according to claim 28 where the first material is a mixture of materials, the second material is a mixture of materials, or both.
30. The apparatus according to claim 28 where the contaminant is water adsorbed by the first material in a first contaminant adsorbent layer along a fluid feed direction.
31. The apparatus according to claim 28 where the first material and the second material are separated.
32. The apparatus according to claim 28 where the first material can be fluidly isolated from the second material upon shutdown.
33. The apparatus according to claim 33 having a shut off valve in a fluid path between the first zone and the second zone.
34 The apparatus according to claim 32 where the first material is housed in a first module separate from a second module housing the second material, the apparatus further having an isolation valve in a fluid path between the first module and the second module.
35. The apparatus according to claim 18 further comprising a parking seal.
36. The apparatus according to claim 18 where the PSA apparatus is a fast cycle, rotary PSA apparatus.
37. The apparatus according to claim 36 where the rotary PSA apparatus operates at a cycle frequency of at least 30 cycles per minute.
38. The apparatus according to claim 18 comprising check valves to prevent forward flow from a zone having the first material to a zone having the second material except during normal operation of the PSA module, the check valve being actuated by an actuator.
39. The apparatus according to claim 38 where the contaminant is water, the adsorber includes a first material acting as a desiccant to adsorb the water in a first zone, the adsorber including a second material in a second zone along a feed direction.
40. A fast cycle, rotary PSA apparatus, comprising:
a breather fluidly coupled to a feed end;
a rotor for housing adsorbers and rotating the adsorbers to receive feed gas from the plenum at normal process rotary speeds at least as high as 30 cycles per minute;
plural adsorbers housed in the rotor and having a first end which receives feed gas and a second end positioned to deliver product gas purified by a pressure swing adsorption process to a product delivery compartment, the adsorbers comprising at least a first material for removing a contaminant and a second material for purifying a product gas;

seals for sealing a buffer chamber about the product delivery compartment, the buffer chamber receiving a gas having a contaminant content substantially the same as or less than the product gas; and at least one contaminant-adsorbent material in a product delivery conduit or a light reflux conduit.
41. The apparatus according to claim 40 where the contaminant is water.
42. The apparatus according to claim 40 where the breather includes at least a desiccant material to remove water.
43. The apparatus according to claim 40 comprising a first compartment for housing the first material and a second compartment for housing the second material with an isolation valve in a fluid path therebetween for fluidly isolating the first compartment from the second compartment.
44. The apparatus according to claim 40 and further comprising desiccant compartments for placing desiccant adjacent at least one valve or at least one port.
45. The apparatus according to claim 40 where the product delivery conduit includes an isolation valve to reduce back diffusion or mixing of a second gas having a higher contaminant content than the product gas into the product delivery conduit.
46. The apparatus according to claim to claim 40 and further comprising an auxiliary contaminant-adsorbent material that is regenerated during normal operation by product gas.
47. The apparatus according to claim 48 where the contaminant-adsorbent material having adsorbed contaminant is regenerated by a gas having a contaminant concentration sufficiently low to result in desorption of contaminant from the contaminant-adsorbent material, a thermal swing, or a combination thereof.
48. The apparatus according to claim 40 further comprising an auxiliary contaminant adsorbent bed, whereby substantially complete regeneration of the contaminant-adsorbent material is achieved by a displacement purge to transfer adsorbed contaminant vapor from a contaminant-adsorbent layer to an auxiliary contaminant-adsorbent bed.
49. The apparatus according to claim 40 where the contaminant is water, the apparatus further having an auxiliary desiccant bed with a water vapor capacity sufficient to adsorb substantially all the water vapor desorbed from the first material.
50. The apparatus according to claim 40 having an exhaust purge valve open during normal operation to discharge exhaust gas, an isolation valve for isolating an auxiliary contaminant-adsorbent bed for countercurrent regeneration flow of a gas having a contaminant concentration sufficiently low to result in desorption of contaminant from the contaminant-adsorbent material, and a gas reflex valve for isolating gas reflex during countercurrent regeneration flow through the auxiliary contaminant-adsorbent bed.
51. The apparatus according to claim 49 where further including a humidity sensor for sensing water vapor from the auxiliary desiccant bed.
52. The apparatus according to claim 40 further comprising heating means for heating the first material.
53. The apparatus according to claim 40 where the adsorbers have plural contaminant adsorbent zones, plural adsorbent zones for purifying gas product, or both.
54. The apparatus according to claim 40 further comprising a parking seal.
55. The apparatus according to claim 40 including an isolation valve in a fluid path between the breather conduit and the adsorbers to prevent flow to the feed ends of the adsorbers.
56. The apparatus according to claim 40 where the breather is an inflated bag diaphragm.
57. The apparatus according to claim 40 where the breather is fluidly coupled to an auxiliary desiccant bed external to the PSA module.
58. The apparatus according to claim 57 where the auxiliary desiccant bed further comprises hearing means.
59. The apparatus according to claim 40 further comprising a desiccant fluidly coupled to or positioned around or about the product delivery conduit.
60. The apparatus according to claim 40 further comprising a desiccant in at least one product reflux delivery conduit.
61. The apparatus according to claim 62 further comprising desiccant traps inline and means for rotating desiccant traps between the product reflux lines and the product line, for displacement purged regeneration by the product.
62. The apparatus according to claim 63 where the means for rotating comprises a rotary adsorption module that rotates through discrete fractional rotations at discrete intervals to switch desiccant beds from humidity adsorption from each of several product reflux loops to regeneration when fluidly coupled to the product.
63. A PSA apparatus, comprising:
at least one adsorber having at least one contaminant-sensitive adsorbent with a feed end and a product end for delivering a product gas enriched in a desired product produced by pressure swing adsorption over the adsorbent;
at least one circumferential seal adjacent the product end for maintaining separation of a first gas on a first side of the circumferential seal from a second gas on a second side of the circumferential seal, with intermittent or continuous relative movement between the circumferential seal and a second component of the apparatus; and at least one buffer seal intended to maintain separation of a first contaminant-comprising gas on a first side of the buffer seal from a second gas desirably isolated from the contaminant where there is intermittent or continuous relative movement between the buffer seal and a second component of the apparatus, the circumferential seal and the buffer seal defining a buffer space comprising at least one buffer chamber having an entry aperture and an exit aperture that provides for flow of a buffer gas in a direction from the circumferential seal to the buffer seal.
64. The apparatus according to claim 63 where the second component of the apparatus is a mating component of the circumferential seal or the buffer seal.
65. The apparatus according to claim 63 where the contaminant is water.
66. A PSA apparatus operating at a PSA cycle frequency of 30 cycles per minute or greater, comprising:
at least one adsorber having at least one contaminant-sensitive adsorbent with a feed end and a product end for delivering a product gas enriched in a desired product produced by pressure swing adsorption over the adsorbent;
at least one circumferential seal adjacent the product end for maintaining separation of a first gas on a first side of the circumferential seal from a second gas on a second side of the circumferential seal, with intermittent or continuous relative movement between the circumferential seal and a second component of the apparatus;
at least one buffer seal intended to maintain separation of a first contaminant-comprising gas on a first side of the buffer seal from a second gas desirably isolated from the contaminant where there is intermittent or continuous relative movement between the seal and a second component of the apparatus, the circumferential seal and the buffer seal defining a buffer space comprising at least one buffer chamber.
67. The apparatus according to claim 66 where the contaminant is water.
68. The apparatus according to claim 66 where the circumferential seal and the buffer seal define a buffer space comprising plural buffer chambers defined by plural dynamic seals for minimizing contaminant flow therebetween, where a buffer chamber other than the buffer chamber immediately adjacent the circumferential seal has a first aperture and a second aperture that allow gas flow through the buffer chambers.
69. The apparatus according to claim 68 where plural buffer chambers other than the buffer chamber immediately adjacent the circumferential seal have a first aperture and a second aperture that allow gas flow through the buffer chambers.
70. The apparatus according to claim 68 where the circumferential seal and the buffer seal define a buffer space comprising at least one buffer chamber defined by plural dynamic seals for partitioning two gases therebetween, the buffer chamber being at a lower pressure than the contaminant-comprising gas.
71. The apparatus according to claim 70 further comprising reducing the pressure of the buffer chamber relative to the contaminant-comprising gas using a vacuum pump.
72. The apparatus according to claim 70 further comprising a conduit from the buffer chamber to an exhaust.
73. The apparatus according to claim 70 further comprising a conduit from the buffer chamber to atmosphere.
74. The apparatus according to claim 66 where the buffer chamber comprises a contaminant-adsorbent material.
75. The apparatus according to claim 66 where the apparatus is a rotary PSA
apparatus.
76. The apparatus according to claim 66 further comprising at least one parking seal.
77. The apparatus according to claim 66 further comprising at least one contaminant-adsorbent material in a product delivery conduit, a reflux line, or both.
78. A PSA apparatus, comprising at least one adsorber having at least one contaminant-adsorbent layer and at least one contaminant-sensitive adsorbent with a feed end and a product end for delivering a product gas enriched in a desired product purified by pressure swing adsorption over the contaminant-sensitive adsorbent, the contaminant-adsorbent layer being effective to ensure that a contaminant concentration of the gas from the contaminant-adsorbent layer is no greater than that of the contaminant concentration in gas from the contaminant-sensitive adsorbent.
79. A method for reducing adsorbent degradation by contaminant adsorption while purifying a product gas in a pressure swing adsorption process, comprising:

providing a PSA apparatus comprising adsorbers with contaminant-sensitive adsorbents having a feed end fluidly coupled to a breather through an isolation valve; and using the PSA apparatus to purify a product gas.
80. The method according to claim 79 where the contaminant is water.
81. The method according to claim 79 where the PSA apparatus is a fast cycle apparatus.
82. The method according to claim 79 where the PSA apparatus is a rotary apparatus operating at a cycle frequency of at least 30 cycles per minute.
83. The method according to claim 79 where the adsorbers comprise a first desiccant material and a second material for purifying a product gas by a pressure swing.
84. The method according to claim 83 having a first zone with the first material, the first zone being isolated on shutdown from an adsorbent zone having the second material sensitive to water by an isolation valve in a fluid path between the desiccant zone and the adsorbent zone.
85. The method according to claim 79 further comprising introducing to a product delivery compartment a product gas produced by pressure swing adsorption over the adsorbers.
86. A method for reducing adsorbent degradation while purifying a product gas in a pressure swing adsorption process, comprising:
providing a fast cycle PSA apparatus comprising adsorbers having contaminant-sensitive adsorbents with a product end fluidly coupled to a product delivery compartment that receives a buffer gas having a contaminant content substantially the same as or less than a product gas produced by a pressure swing adsorption process over the adsorbers; and using the PSA apparatus to purify a product gas.
87. The method according to claim 86 where the PSA apparatus further comprises a breather fluidly coupled to a feed end through an isolation valve in a fluid path between the breather and the adsorbers.
88. The method according to claim 86 where the PSA apparatus further comprises a breather fluidly coupled to a feed plenum, a rotor for housing adsorbers and rotating the adsorbers to receive feed gas from the plenum at normal process rotary speeds at least as high as 30 cycles per minute, plural adsorbers housed in the rotor and having a first end which receives feed gas from the feed plenum and a second end positioned to deliver product gas produced by a pressure swing adsorption process to a product delivery compartment, the adsorbers comprising at least a first desiccant zone and a second adsorbent zone, seals for sealing a buffer chamber about the light product delivery compartment, the buffer chamber receiving a gas having a water vapor content the same as or less than the product gas, and a product delivery conduit for delivering a desired product gas.
89. A method for shutting down a PSA apparatus according to a shutdown sequence, comprising:
operating a rotary PSA apparatus having a feed end fluidly coupled to a first end of adsorbers that include a first material for adsorbing a contaminant and at least one contaminant-sensitive adsorbent for purifying a product gas by pressure swing adsorption, the PSA apparatus further including a product end coupled to a second end of the adsorbers for delivering a product gas;
discontinuing product gas delivery;
exhausting feed gas;
introducing a blanket gas into a feed end of the PSA apparatus;
discontinuing delivery of gas feed mixture to the feed end; and purging the adsorbers with a purge gas.
90. The method according to claim 89 and further comprising preparing the apparatus for elevated pressure parking, the method comprising closing an exhaust port and introducing a blanket gas into the feed end to pressurize the apparatus to a pressure above ambient.
91. The method according to claim 89 further comprising discontinuing rotor rotation and engaging any parking seal.
92. The method according to claim 89 and further comprising heating the first material to facilitate desorption of adsorbed contaminant.
93. The method according to claim 89 where the contaminant is water.
94. The method according to claim 93 where the first material is a desiccant and further comprising cooling the desiccant after purge.
95. The method according to claim 94 where a target water vapor pressure at the product end is substantially that of the selected adsorbent material at the product end.
95. The method according to claim 89 where the adsorbers are purged using a purge gas having a water vapor content substantially equal to a water vapor content of the product gas produced by a PSA process over the adsorbers
96. A method for shutting down a PSA apparatus according to a shutdown sequence, comprising:
operating a rotary PSA apparatus having a feed end fluidly coupled to a first end of adsorbers that include an adsorbent desiccant material to adsorb water and at least one water-sensitive adsorbent and a product end coupled to a second end of the adsorbers for delivering a product gas;
discontinuing delivery of product gas;
exhausting feed gas;
introducing a blanket gas into a feed end of the PSA apparatus;
heating the desiccant to facilitate desorption of adsorbed water;
discontinuing delivery of gas feed mixture to the feed end;
purging the adsorbers with a purge gas having a water vapor content substantially equal to water vapor content of the product gas produced by a PSA process over the adsorbers;
stopping all purge operations;

closing an exhaust port and introducing a second blanket gas into the feed end to pressurize the apparatus to a pressure above ambient;
discontinuing rotor rotation; and engaging any parking seal.
97. The method according to claim 96 comprising placing a desiccant in at least one light reflux line of the PSA apparatus.
98. The method according to claim 96 where desiccant activity is maintained by periodic regeneration or replacement.
99. The method according to claim 96 and further comprising placing a desiccant trap in the product line.
100. The method according to claim 96 where the purge gas is at a temperature higher than the adsorbers and purging the adsorbers with the adsorber purge gas heats the adsorbers.
101. The method according to claim 96 where the adsorber purge gas is the product gas.
102. The method according to claim 96 and further comprising heating the desiccant with heating means.
103. The method according to claim 102 where the heating means comprises using microwave or infrared radiation generating means.
104. The method according to claim 96 where the product gas is recirculated through an auxiliary desiccant bed prior to purging the adsorbers.
105. A method for increasing operation time before shutdown is required of a rotary fast cycle PSA apparatus, comprising:
providing a PSA unit having a feed air dryer upstream of a feed end of the PSA
unit, and adsorbers having a desiccant layer at the feed end of the adsorbers; and operating the PSA unit under normal operating conditions useful for purifying a product gas.
106. The method according to claim 105 where the adsorbers are provided as high surface area laminated adsorbers, with the adsorbent supported in thin adsorbent sheets separated by spacers to define flow channels between adjacent sheets.
107. The method according to claim 106 where the laminated adsorbers include a desiccant layer for adsorbing water at the feed end of the sheets.
108. The method according to claim 105 and further comprising providing a buffer space between the internal working zone of valves communicating to the product ends of the adsorbers, the buffer space being a positive pressured, dry gas flushed zone.
109. The method according to claim 108 further comprising flushing the buffer spacer with flushing circulation provided by delivered product flow.
110. A method for producing a positive pressure park mode in a fast cycle, rotary PSA apparatus, comprising:
shutting down a rotating PSA system to reduce desiccant water loading;
introducing a gas into a feed end of the apparatus to provide a park pressure above ambient;
closing all ports and discontinuing rotor rotation; and engaging a parking seal.
111. A method for shutting down a PSA apparatus according to a shutdown sequence, comprising:
operating a PSA apparatus having a feed end fluidly coupled to a first end of adsorbers that include a contaminant adsorbent layer comprising a contaminant adsorbent material and at least one contaminant-sensitive adsorbent, the PSA apparatus further including a product end coupled to a second end of the adsorbers for delivering a product gas;
stopping delivery of product gas;
purging adsorbers with product flow; and heating the contaminant adsorbent layer.
112. The method according to claim 111 and further comprising cooling the adsorbers.
113. The method according to claim 112 comprising directly heating the contaminant adsorbent layer using heating means.
114. The method according to claim 113 where the heating means comprise resistance heating, microwave heating, infra red heating, seal friction, reducing cooling load, or combinations thereof.
115. The method according to claim 137 where the contaminant adsorbent layer is a desiccant layer.
116. The method according to claim 115 where the desiccant layer is heated by gas flow.
117. A method for reducing adsorbent degradation by moisture adsorption while purifying a product gas in a pressure swing adsorption process, comprising:
providing a PSA apparatus comprising adsorbers with a second water-sensitive adsorber material receiving a feed gas, the feed gas contacting a first water vapor removal layer, which has been designed so that the adsorber material, which performs the main separation, suffers a limited, controlled level of deactivation when the contaminant has broken through second material product gas and has reached equilibrium; and using the PSA apparatus to produce a gas.
118. The method according to claim 117 where the PSA apparatus is a fast cycle apparatus.
119. The method according to claim 117 where the adsorbers comprise a first material that acts as a desiccant to adsorb water and a second material to purify a product gas by a pressure swing.
CA002329475A 2000-12-11 2000-12-11 Fast cycle psa with adsorbents sensitive to atmospheric humidity Abandoned CA2329475A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
CA002329475A CA2329475A1 (en) 2000-12-11 2000-12-11 Fast cycle psa with adsorbents sensitive to atmospheric humidity
EP01991154A EP1355717A4 (en) 2000-12-11 2001-12-11 Psa with adsorbents sensitive to contaminants
AU2002230897A AU2002230897A1 (en) 2000-12-11 2001-12-11 Psa with adsorbents sensitive to contaminants
US10/021,751 US7037358B2 (en) 2000-12-11 2001-12-11 PSA with adsorbents sensitive to contaminants
CNB018204244A CN100371051C (en) 2000-12-11 2001-12-11 PSA with adsorbents sensitive to contaminants
CA002430156A CA2430156C (en) 2000-12-11 2001-12-11 Psa with adsorbents sensitive to contaminants
PCT/US2001/048569 WO2002047797A1 (en) 2000-12-11 2001-12-11 Psa with adsorbents sensitive to contaminants
JP2002549362A JP2004515349A (en) 2000-12-11 2001-12-11 Pressure swing adsorption using contaminant-sensitive adsorbents
US10/851,755 US7160367B2 (en) 2000-12-11 2004-05-20 PSA with adsorbents sensitive to contaminants

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA002329475A CA2329475A1 (en) 2000-12-11 2000-12-11 Fast cycle psa with adsorbents sensitive to atmospheric humidity

Publications (1)

Publication Number Publication Date
CA2329475A1 true CA2329475A1 (en) 2002-06-11

Family

ID=4167983

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002329475A Abandoned CA2329475A1 (en) 2000-12-11 2000-12-11 Fast cycle psa with adsorbents sensitive to atmospheric humidity

Country Status (7)

Country Link
US (2) US7037358B2 (en)
EP (1) EP1355717A4 (en)
JP (1) JP2004515349A (en)
CN (1) CN100371051C (en)
AU (1) AU2002230897A1 (en)
CA (1) CA2329475A1 (en)
WO (1) WO2002047797A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008089563A1 (en) * 2007-01-24 2008-07-31 Xebec Adsorption Inc. Guard layers for rapid cycle pressure swing adsorption devices
CN114931845A (en) * 2021-12-31 2022-08-23 安徽华塑股份有限公司 Industrial hydrous hydrogen chloride gas dehydration equipment

Families Citing this family (146)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094275B2 (en) * 1997-12-01 2006-08-22 Questair Technologies, Inc. Modular pressure swing adsorption apparatus
WO2002035623A2 (en) 2000-10-27 2002-05-02 Questair Technologies Inc. Systems and processes for providing hydrogen to fuel cells
US7300905B2 (en) * 2001-01-05 2007-11-27 Questair Technologies Inc. Methods for their manufacture of adsorbent
US7838708B2 (en) 2001-06-20 2010-11-23 Grt, Inc. Hydrocarbon conversion process improvements
WO2003076048A1 (en) * 2002-03-14 2003-09-18 Questair Technologies Inc. Gas separation by combined pressure swing and displacement purge
EP1486143B1 (en) * 2002-03-19 2014-12-24 Panasonic Corporation Air conditioning seat device
WO2004067684A2 (en) * 2003-01-30 2004-08-12 Questair Technologies, Inc. Compact synthesis gas generation system
US20050171393A1 (en) 2003-07-15 2005-08-04 Lorkovic Ivan M. Hydrocarbon synthesis
RU2366642C2 (en) 2003-07-15 2009-09-10 Джи Ар Ти, Инк. Hydrocarbons synthesis
US7674941B2 (en) 2004-04-16 2010-03-09 Marathon Gtf Technology, Ltd. Processes for converting gaseous alkanes to liquid hydrocarbons
US8642822B2 (en) 2004-04-16 2014-02-04 Marathon Gtf Technology, Ltd. Processes for converting gaseous alkanes to liquid hydrocarbons using microchannel reactor
US7244867B2 (en) 2004-04-16 2007-07-17 Marathon Oil Company Process for converting gaseous alkanes to liquid hydrocarbons
US20080275284A1 (en) 2004-04-16 2008-11-06 Marathon Oil Company Process for converting gaseous alkanes to liquid hydrocarbons
US20060100469A1 (en) 2004-04-16 2006-05-11 Waycuilis John J Process for converting gaseous alkanes to olefins and liquid hydrocarbons
US8173851B2 (en) 2004-04-16 2012-05-08 Marathon Gtf Technology, Ltd. Processes for converting gaseous alkanes to liquid hydrocarbons
US7101414B2 (en) * 2004-04-27 2006-09-05 Munters Corporation Rotary bed sorption system including at least one recycled isolation loop, and methods of designing and operating such a system
US20060048648A1 (en) * 2004-08-20 2006-03-09 Questair Technologies Inc. Parallel passage contactor structure
US20060090646A1 (en) * 2004-11-04 2006-05-04 Questair Technologies Inc. Adsorbent material for selective adsorption of carbon monoxide and unsaturated hydrocarbons
JP2008526494A (en) * 2005-01-07 2008-07-24 クエストエアー テクノロジーズ インコーポレイテッド Engineering adsorption structure for velocity separation
CN101146592B (en) * 2005-03-24 2010-10-06 恩必安有限公司 The system of treating odor and hazardrous gas with rotary regenerative heat exchanger and its apparatus
JP3879762B2 (en) * 2005-03-29 2007-02-14 ダイキン工業株式会社 Humidity control device
US7763098B2 (en) * 2005-11-18 2010-07-27 Xebec Adsorption Inc. Rapid cycle syngas pressure swing adsorption system
CA2641348C (en) 2006-02-03 2014-12-23 Grt, Inc. Continuous process for converting natural gas to liquid hydrocarbons
KR101335397B1 (en) 2006-02-03 2013-12-02 지알티, 인코포레이티드 Separation of light gases from halogens
US7854793B2 (en) * 2006-06-30 2010-12-21 David Lester Rarig Pressure swing adsorption system with indexed rotatable multi-port valves
FR2906160B1 (en) 2006-09-25 2009-06-05 Air Liquide PSA METHOD WITH COMPOSITE ADSORPTION BED FORMED OF ADSORBENT AND AGGLOMERATS OF MCP
US8016918B2 (en) 2006-10-04 2011-09-13 Air Products And Chemicals, Inc. Performance stability in rapid cycle pressure swing adsorption systems
US7717981B2 (en) 2006-10-04 2010-05-18 Air Products And Chemicals, Inc. Performance stability in shallow beds in pressure swing adsorption systems
US20090071333A1 (en) * 2006-10-04 2009-03-19 Air Products And Chemicals, Inc. Performance Stability in Shallow Beds in Pressure Swing Adsorption Systems
JP2008149296A (en) * 2006-12-20 2008-07-03 Teijin Pharma Ltd Oxygen concentrator
EP2114555B1 (en) * 2007-01-24 2017-10-04 Air Products and Chemicals, Inc. Seal assembly for gas separation device
US8529663B2 (en) * 2007-05-18 2013-09-10 Exxonmobil Research And Engineering Company Process for removing a target gas from a mixture of gases by swing adsorption
US8444750B2 (en) * 2007-05-18 2013-05-21 Exxonmobil Research And Engineering Company Removal of CO2, N2, or H2S from gas mixtures by swing adsorption with low mesoporosity adsorbent contactors
US7959720B2 (en) 2007-05-18 2011-06-14 Exxonmobil Research And Engineering Company Low mesopore adsorbent contactors for use in swing adsorption processes
JP5401447B2 (en) * 2007-05-18 2014-01-29 エクソンモービル リサーチ アンド エンジニアリング カンパニー Removal of target gas from gas mixture by swing adsorption with turbo expander
US8529662B2 (en) 2007-05-18 2013-09-10 Exxonmobil Research And Engineering Company Removal of heavy hydrocarbons from gas mixtures containing heavy hydrocarbons and methane
US8545602B2 (en) 2007-05-18 2013-10-01 Exxonmobil Research And Engineering Company Removal of CO2, N2, and H2S from gas mixtures containing same
CA2688551C (en) * 2007-05-18 2013-09-10 Exxonmobil Research And Engineering Company Process for removing a target gas from a mixture of gases by thermal swing adsorption
JP2010528054A (en) 2007-05-24 2010-08-19 ジーアールティー インコーポレイテッド Zone reactor incorporating reversible hydrogen halide capture and release
JP4798076B2 (en) * 2007-06-27 2011-10-19 株式会社Ihi Oxygen concentrator
US20090065007A1 (en) 2007-09-06 2009-03-12 Wilkinson William R Oxygen concentrator apparatus and method
US20090084363A1 (en) * 2007-09-27 2009-04-02 Gm Global Technology Operations, Inc. Regeneration of Evaporative Emision Control System for Plug-in Hybrid Vehicle
JP2009089831A (en) * 2007-10-05 2009-04-30 Ngk Spark Plug Co Ltd Oxygen concentrator
WO2009064569A1 (en) * 2007-11-12 2009-05-22 Exxonmobil Upstream Research Company Methods of generating and utilizing utility gas
JP5577324B2 (en) * 2008-04-30 2014-08-20 エクソンモービル アップストリーム リサーチ カンパニー Method and apparatus for removing oil from a utility gas stream
US8413655B2 (en) * 2008-06-10 2013-04-09 Micropore, Inc. Adsorbents and inhalation devices
US8282810B2 (en) * 2008-06-13 2012-10-09 Marathon Gtf Technology, Ltd. Bromine-based method and system for converting gaseous alkanes to liquid hydrocarbons using electrolysis for bromine recovery
US20090320928A1 (en) * 2008-06-30 2009-12-31 Uop Llc Multi-track rotary valve in combination with a pressure reducer and method for operating the combination
KR101740419B1 (en) 2008-07-18 2017-05-26 지알티, 인코포레이티드 Continuous process for converting natural gas to liquid hydrocarbons
US8602087B2 (en) * 2008-11-19 2013-12-10 Tai-Her Yang Double flow-circuit heat exchange device for periodic positive and reverse directional pumping
JP2010051877A (en) * 2008-07-30 2010-03-11 Jfe Steel Corp Apparatus and method for manufacturing oxygen enriched air
US8211312B2 (en) * 2009-03-27 2012-07-03 Uop Llc Separation system and method
US8551230B2 (en) * 2009-06-08 2013-10-08 7142871 Canada Inc. PH2OCP—portable water and climatic production system
US8545609B2 (en) * 2009-06-08 2013-10-01 7142871 Canada Inc. Microwave reactivation system for standard and explosion-proof dehumidification system
EP2528677B1 (en) * 2010-01-26 2017-08-23 Micropore, Inc. Adsorbent system for removal of gaseous contaminants
CN101745245B (en) * 2010-02-05 2012-05-23 北京化工大学 Multi-level countercurrent rotating bed reaction and rectification device and application thereof
US8198495B2 (en) 2010-03-02 2012-06-12 Marathon Gtf Technology, Ltd. Processes and systems for the staged synthesis of alkyl bromides
US8367884B2 (en) 2010-03-02 2013-02-05 Marathon Gtf Technology, Ltd. Processes and systems for the staged synthesis of alkyl bromides
US8343259B2 (en) * 2010-03-29 2013-01-01 Wearair Oxygen, Inc. Moisture mitigation in PSA air fractionation
US8920996B2 (en) 2010-05-11 2014-12-30 Dcns Systems and methods for regulating fuel cell air flow during low loads or cold temperature operation
US8449649B2 (en) 2010-05-11 2013-05-28 Idatech, Llc Systems and methods for starting up pressure swing adsorption assemblies and hydrogen-producing fuel processing systems including the same
WO2011149640A1 (en) 2010-05-28 2011-12-01 Exxonmobil Upstream Research Company Integrated adsorber head and valve design and swing adsorption methods related thereto
US20110296858A1 (en) * 2010-06-02 2011-12-08 7291345 Canada Inc. Ph2ocp portable water and climatic production system
US20120055474A1 (en) 2010-09-07 2012-03-08 Wilkinson William R Methods and systems for providing oxygen enriched gas
US20120055483A1 (en) * 2010-09-07 2012-03-08 Wilkinson William R Shutdown system and method for an oxygen concentrator
US8616207B2 (en) 2010-09-07 2013-12-31 Inova Labs, Inc. Oxygen concentrator heat management system and method
US8695633B2 (en) 2010-09-09 2014-04-15 Uop Llc Control of rotary valve operation for reducing wear
US8821619B2 (en) 2010-10-14 2014-09-02 Micropore, Inc. Adsorbent cartridge assembly with end cap
TWI495501B (en) 2010-11-15 2015-08-11 Exxonmobil Upstream Res Co Kinetic fractionators, and cycling processes for fractionation of gas mixtures
US8920732B2 (en) 2011-02-15 2014-12-30 Dcns Systems and methods for actively controlling steam-to-carbon ratio in hydrogen-producing fuel processing systems
WO2012118755A1 (en) 2011-03-01 2012-09-07 Exxonmobil Upstream Research Company Apparatus and systems having an encased adsorbent contractor and swing adsorption processes related thereto
MX2013008387A (en) 2011-03-01 2013-08-12 Exxonmobil Upstream Res Co Methods of removing contaminants from a hydrocarbon stream by swing adsorption and related apparatus and systems.
CA2824162A1 (en) 2011-03-01 2012-09-07 Exxonmobil Upstream Research Company Apparatus and systems having a rotary valve assembly and swing adsorption processes related thereto
EP2680954B1 (en) 2011-03-01 2018-09-12 Exxonmobil Upstream Research Company Methods of removing contaminants from a hydrocarbon stream by pressure swing adsorption and related apparatus and systems
US9017457B2 (en) 2011-03-01 2015-04-28 Exxonmobil Upstream Research Company Apparatus and systems having a reciprocating valve head assembly and swing adsorption processes related thereto
US9352269B2 (en) 2011-03-01 2016-05-31 Exxonmobil Upstream Research Company Apparatus and systems having a rotary valve assembly and swing adsorption processes related thereto
EP2680947A4 (en) 2011-03-01 2015-04-29 Exxonmobil Upstream Res Co Apparatus and systems having compact configuration multiple swing adsorption beds and methods related thereto
US8815050B2 (en) 2011-03-22 2014-08-26 Marathon Gtf Technology, Ltd. Processes and systems for drying liquid bromine
US8753430B2 (en) 2011-05-10 2014-06-17 Uop Llc Affixing a seal sheet to a rotor of a rotary valve
US8436220B2 (en) 2011-06-10 2013-05-07 Marathon Gtf Technology, Ltd. Processes and systems for demethanization of brominated hydrocarbons
US8829256B2 (en) 2011-06-30 2014-09-09 Gtc Technology Us, Llc Processes and systems for fractionation of brominated hydrocarbons in the conversion of natural gas to liquid hydrocarbons
US8802908B2 (en) 2011-10-21 2014-08-12 Marathon Gtf Technology, Ltd. Processes and systems for separate, parallel methane and higher alkanes' bromination
US9193641B2 (en) 2011-12-16 2015-11-24 Gtc Technology Us, Llc Processes and systems for conversion of alkyl bromides to higher molecular weight hydrocarbons in circulating catalyst reactor-regenerator systems
WO2013108172A1 (en) * 2012-01-16 2013-07-25 Koninklijke Philips N.V. Arrangement and method for generating oxygen
KR20150014466A (en) 2012-04-24 2015-02-06 마이크로포어, 인코포레이티드 Durable adsorbent material and adsorbent packs
WO2013171628A1 (en) 2012-05-16 2013-11-21 Koninklijke Philips N.V. Oxygen separator and method of generating oxygen
CN102755810A (en) * 2012-08-02 2012-10-31 南京圣火水泥新技术工程有限公司 Rotor type pressure swing adsorption gas separation device
US9034078B2 (en) 2012-09-05 2015-05-19 Exxonmobil Upstream Research Company Apparatus and systems having an adsorbent contactor and swing adsorption processes related thereto
NZ707159A (en) 2012-10-12 2018-06-29 Inova Labs Inc Dual oxygen concentrator systems and methods
AU2013328916A1 (en) * 2012-10-12 2015-05-14 Inova Labs, Inc. Oxygen concentrator systems and methods
WO2014059405A1 (en) 2012-10-12 2014-04-17 Inova Labs, Inc. Method and systems for the delivery of oxygen enriched gas
EP2845638B1 (en) 2013-09-09 2018-08-22 Kaeser Kompressoren Se Method for operating an adsorbing device, and control device
EP3094560A1 (en) * 2013-12-18 2016-11-23 Carleton Life Support Systems, Inc. Air drying system for obogs
US9440179B2 (en) 2014-02-14 2016-09-13 InovaLabs, LLC Oxygen concentrator pump systems and methods
CN105013291A (en) * 2014-05-01 2015-11-04 刘海 Carrying type molecule capture and separation device
WO2016014232A1 (en) 2014-07-25 2016-01-28 Exxonmobil Upstream Research Company Apparatus and system having a valve assembly and swing adsorption processes related thereto
EP3218326B1 (en) 2014-11-11 2020-03-04 ExxonMobil Upstream Research Company High capacity structures and monoliths via paste imprinting
US9713787B2 (en) 2014-12-10 2017-07-25 Exxonmobil Upstream Research Company Adsorbent-incorporated polymer fibers in packed bed and fabric contactors, and methods and devices using same
CA2970307C (en) 2014-12-23 2019-10-22 Exxonmobil Upstream Research Company Structured adsorbent beds, methods of producing the same and uses thereof
WO2016186725A1 (en) 2015-05-15 2016-11-24 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto comprising mid-bed purge systems
US9751041B2 (en) 2015-05-15 2017-09-05 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto
US9458013B1 (en) 2015-05-27 2016-10-04 Air Products And Chemicals, Inc. Process for the production of hydrogen
WO2017039991A1 (en) 2015-09-02 2017-03-09 Exxonmobil Upstream Research Company Process and system for swing adsorption using an overhead stream of a demethanizer as purge gas
US10293298B2 (en) 2015-09-02 2019-05-21 Exxonmobil Upstream Research Company Apparatus and system for combined temperature and pressure swing adsorption processes related thereto
EP3368189A1 (en) 2015-10-27 2018-09-05 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto having a plurality of valves
WO2017074655A1 (en) 2015-10-27 2017-05-04 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto having a plurality of valves
WO2017074657A1 (en) 2015-10-27 2017-05-04 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto having actively-controlled feed poppet valves and passively controlled product valves
KR20180083911A (en) 2015-11-16 2018-07-23 엑손모빌 업스트림 리서치 캄파니 Adsorption method of adsorbent and carbon dioxide
JP2019508245A (en) 2016-03-18 2019-03-28 エクソンモービル アップストリーム リサーチ カンパニー Apparatus and system for swing adsorption process
JP6980686B2 (en) * 2016-03-31 2021-12-15 スヴァンテ インコーポレイテッド Low thermal conductivity adsorption gas separator
WO2017192660A1 (en) 2016-05-03 2017-11-09 Inova Labs, Inc. Method and systems for the delivery of oxygen enriched gas
FR3051374B1 (en) 2016-05-18 2018-05-18 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude PROCESS FOR PRODUCING VSA-TYPE OXYGEN WITH PERIODIC REGENERATION
US10863638B2 (en) * 2016-05-24 2020-12-08 Eaton Intelligent Power Limited Moisture control systems for enclosures
CN109219476A (en) 2016-05-31 2019-01-15 埃克森美孚上游研究公司 For becoming the device and system of adsorption method
WO2017209861A1 (en) 2016-05-31 2017-12-07 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes
US10434458B2 (en) 2016-08-31 2019-10-08 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes related thereto
AU2017320837B2 (en) 2016-09-01 2020-07-23 Exxonmobil Upstream Research Company Swing adsorption processes for removing water using 3A zeolite structures
US10328382B2 (en) 2016-09-29 2019-06-25 Exxonmobil Upstream Research Company Apparatus and system for testing swing adsorption processes
KR102260066B1 (en) 2016-12-21 2021-06-04 엑손모빌 업스트림 리서치 캄파니 Self-supporting structure with foamed geometry and active material
AU2017379684B2 (en) 2016-12-21 2020-03-12 Exxonmobil Upstream Research Company Self-supporting structures having active materials
DE102017000518A1 (en) * 2017-01-23 2018-07-26 Donaldson Filtration Deutschland Gmbh Reprocessing tank, cartridge and device for treating a fluid with two treatment tanks
WO2019002075A1 (en) 2017-06-27 2019-01-03 Koninklijke Philips N.V. Portable oxygen concentrator sieve bed
US10765991B2 (en) 2017-08-10 2020-09-08 Air Products And Chemicals, Inc. Rapid cycle pressure swing adsorption process and adsorbent laminates for use therein
CN107715645A (en) * 2017-09-30 2018-02-23 广州市鑫衡运科技有限公司 A kind of waste gas recovering device and gas recovery method
WO2019147516A1 (en) 2018-01-24 2019-08-01 Exxonmobil Upstream Research Company Apparatus and system for temperature swing adsorption
WO2019168628A1 (en) 2018-02-28 2019-09-06 Exxonmobil Upstream Research Company Apparatus and system for swing adsorption processes
US11177494B2 (en) 2018-03-05 2021-11-16 H2 Powertech, Llc Systems and methods for forming a liquid mixture having a predetermined mix ratio and reforming systems, reforming methods, fuel cell systems, and fuel cell methods that utilize the liquid mixture
CN108404601B (en) * 2018-03-30 2024-02-06 中北大学 Gas adsorption equipment of super-gravity movable adsorption bed
CN111054179B (en) * 2018-10-17 2022-02-11 上海深城环保设备工程有限公司 Scanning desorption adsorption concentration device
CN110538620B (en) * 2018-11-14 2021-10-15 北京北方华创微电子装备有限公司 Pressure control system and pressure control method of reaction chamber
US11318410B2 (en) 2018-12-21 2022-05-03 Exxonmobil Upstream Research Company Flow modulation systems, apparatus, and methods for cyclical swing adsorption
CN109876593B (en) * 2019-03-08 2024-01-26 北京科技大学 Radial tube type adsorber and adsorption and desorption method thereof
US11376545B2 (en) 2019-04-30 2022-07-05 Exxonmobil Upstream Research Company Rapid cycle adsorbent bed
BE1027367B1 (en) * 2019-06-13 2021-01-21 Atlas Copco Airpower Nv Static dryer
US20220241720A1 (en) * 2019-08-16 2022-08-04 Atlas Copco Airpower, Naamloze Vennootschap Dryer for compressed gas, compressor installation provided with a dryer and a method for drying compressed gas
BE1027511B1 (en) * 2019-08-16 2021-03-17 Atlas Copco Airpower Nv Dryer for compressed gas, compressor installation equipped with dryer and method for drying compressed gas
US11655910B2 (en) 2019-10-07 2023-05-23 ExxonMobil Technology and Engineering Company Adsorption processes and systems utilizing step lift control of hydraulically actuated poppet valves
US11433346B2 (en) 2019-10-16 2022-09-06 Exxonmobil Upstream Research Company Dehydration processes utilizing cationic zeolite RHO
CN111537643B (en) * 2020-05-22 2022-09-09 无锡工艺职业技术学院 Method for detecting content of heavy metal organic compounds in water in plastic pipeline
CN111530232B (en) * 2020-05-28 2021-08-10 陈孝通 Gas separation device and gas separation method
CN112076617A (en) * 2020-09-10 2020-12-15 奚欢 Energy-saving recovery processing device for nitrogen oxides in industrial production waste gas
CN112456445B (en) * 2020-11-16 2022-05-31 河北金利康科技集团有限公司 Efficient medical oxygen generator and oxygen generation method
CN112629782B (en) * 2020-12-30 2022-09-06 中国工程物理研究院激光聚变研究中心 Self-sealing type vacuum detection system and vacuumizing leak detection method
CA3217072A1 (en) * 2021-05-04 2022-11-10 Tyson Lee Lanigan-Atkins Systems and processes for removal of carbon dioxide (co2) from co2-containing gases using alkali metal adsorbents
CN115215455B (en) * 2022-05-26 2023-09-26 无锡工源环境科技股份有限公司 Efficient antimony removal process for printing and dyeing wastewater and treatment equipment thereof
CN116574543B (en) * 2023-05-29 2023-09-29 南京宇创石化设备有限公司 Liquefied gas desulfurizing tower

Family Cites Families (119)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3094569A (en) * 1958-10-20 1963-06-18 Union Carbide Corp Adsorptive separation process
US3204388A (en) * 1960-02-01 1965-09-07 Atlantic Res Corp Buffer bed dehumidification
GB1144692A (en) * 1965-03-12 1969-03-05 Pall Corp Gas drier with automatic cycle control and process
US3430418A (en) 1967-08-09 1969-03-04 Union Carbide Corp Selective adsorption process
GB1298818A (en) * 1968-12-20 1972-12-06 Kobe Steel Ltd Separation of oxygen from air
US3847672A (en) 1971-08-18 1974-11-12 United Aircraft Corp Fuel cell with gas separator
JPS4856593A (en) * 1971-11-22 1973-08-08
US4019879A (en) 1975-09-26 1977-04-26 Union Carbide Corporation Selective adsorption of carbon monoxide from gas streams
GB1559325A (en) 1976-02-27 1980-01-16 Boc Ltd Gas separation
US4153434A (en) * 1976-04-07 1979-05-08 General Cable Corporation Emergency standby air drying back-up system
US4127395A (en) * 1976-10-18 1978-11-28 Pall Corporation Adsorbent fractionator with fail-safe automatic cycle control and process
US4322394A (en) 1977-10-31 1982-03-30 Battelle Memorial Institute Adsorbent regeneration and gas separation utilizing microwave heating
US4200682A (en) 1979-03-16 1980-04-29 United Technologies Corporation Integrated fuel cell and fuel conversion apparatus
JPS55149620A (en) * 1979-05-11 1980-11-21 Noboru Sato Oxygen-enriching system having good rise-up characteristic
US4272265A (en) 1979-06-22 1981-06-09 Essex Cryogenics Of Missouri, Inc. Apparatus for pressure swing generation of oxygen
US4354859A (en) 1981-08-06 1982-10-19 Union Carbide Corporation Enhanced gas separation by selective adsorption
US4555453A (en) 1981-10-01 1985-11-26 Electric Power Research, Inc. Method for forming molten carbonate fuel cell component and structure
US4406675A (en) * 1981-12-10 1983-09-27 Union Carbide Corporation RPSA Process
GB2117265B (en) 1982-03-13 1986-05-21 Hidefumi Hirai Carbon monoxide adsorbent and method of producing the same
JPS598605A (en) * 1982-07-07 1984-01-17 Osaka Oxgen Ind Ltd Concentration of nitrogen
US4452612A (en) * 1982-09-22 1984-06-05 Cubemco, Inc. Separation and purification of gases and vapors by continuous pressure-swing adsorption
US4539019A (en) * 1983-09-29 1985-09-03 Air Products & Chemicals, Inc. Control system for air fractionation by selective adsorption
US4801308A (en) 1983-10-03 1989-01-31 Keefer Bowie Apparatus and process for pressure swing adsorption separation
US4702903A (en) 1983-10-03 1987-10-27 Keefer Bowie Method and apparatus for gas separation and synthesis
EP0143537B1 (en) 1983-10-03 1990-03-21 Bowie Gordon Keefer Method and apparatus for gas separation and synthesis
US4816121A (en) 1983-10-03 1989-03-28 Keefer Bowie Gas phase chemical reactor
US4726816A (en) 1983-11-08 1988-02-23 Union Carbide Corporation Reformer-pressure swing adsorption process for the production of carbon monoxide
US4578214A (en) 1984-02-06 1986-03-25 C F Braun & Co. Process for ammonia syngas manufacture
US4530705A (en) 1984-04-16 1985-07-23 Firey Joseph C Cyclic gas separator
EP0170884B1 (en) 1984-07-04 1989-01-18 Nippon Kokan Kabushiki Kaisha Method of separating carbon monoxide
JPS6171561A (en) 1984-09-14 1986-04-12 Mitsubishi Heavy Ind Ltd Composite plant of fuel cell
US4783433A (en) 1985-11-19 1988-11-08 Nippon Kokan Kabushiki Kaisha Selective adsorbent for CO and method of manufacturing the same
JPH06103631B2 (en) 1986-01-23 1994-12-14 株式会社日立製作所 Air supply system device for fuel cell system
EP0252596B1 (en) 1986-06-12 1993-10-13 Imperial Chemical Industries Plc Adsorption process
JPS63166702A (en) 1986-12-26 1988-07-09 Osaka Oxygen Ind Ltd Concentration of oxygen gas
US4756723A (en) * 1987-03-04 1988-07-12 Air Products And Chemicals, Inc. Preparation of high purity oxygen
US4968329A (en) 1987-10-26 1990-11-06 Keefer Bowie Pressure swing adsorption for concentration of a gas component
US4917711A (en) 1987-12-01 1990-04-17 Peking University Adsorbents for use in the separation of carbon monoxide and/or unsaturated hydrocarbons from mixed gases
JPH01155945A (en) 1987-12-12 1989-06-19 Kansai Coke & Chem Co Ltd Production of adsorbent for separating and recovering co
US4790858A (en) 1988-01-29 1988-12-13 Air Products And Chemicals, Inc. Fractionation of multicomponent gas mixtures by pressure swing adsorption
US4950311A (en) * 1988-03-07 1990-08-21 White Jr Donald H Heaterless adsorption system for combined purification and fractionation of air
US4963339A (en) 1988-05-04 1990-10-16 The Boc Group, Inc. Hydrogen and carbon dioxide coproduction
JPH01307425A (en) * 1988-06-06 1989-12-12 Kobe Steel Ltd Pressure-swinging adsorber
FR2633847B1 (en) 1988-07-08 1991-04-19 Air Liquide PROCESS FOR TREATING A GAS MIXTURE BY ADSORPTION
JPH02117072A (en) 1988-10-26 1990-05-01 Toyo Eng Corp Fuel cell power generation system
DE3932217A1 (en) 1989-04-25 1990-10-31 Linde Ag METHOD FOR OPERATING HIGH-TEMPERATURE FUEL CELLS
DE3913581A1 (en) 1989-04-25 1990-10-31 Linde Ag METHOD FOR OPERATING FUEL CELLS
CA2044242A1 (en) * 1989-10-27 1991-04-28 Leonard A. Jonas Sorbing apparatus with guard bed
CA2016045C (en) 1990-05-04 1994-08-16 Quest Air Gases Inc. Gas separation by pressure swing adsorption
US5096469A (en) 1990-07-23 1992-03-17 Keefer Bowie Adsorptive gas separator with inertial energy exchange
US5082473A (en) 1990-07-23 1992-01-21 Keefer Bowie Extraction and concentration of a gas component
US5258571A (en) 1990-08-23 1993-11-02 Air Products And Chemicals, Inc. Separations using highly dispersed cuprous compositions
US5126310A (en) 1990-08-23 1992-06-30 Air Products And Chemicals, Inc. Highly dispersed cuprous compositions
FR2667801B1 (en) 1990-10-11 1992-12-04 Air Liquide PROCESS AND EQUIPMENT FOR SEPARATION BY ADSORPTION OF AT LEAST ONE CONSTITUENT OF A GASEOUS MIXTURE.
US5096470A (en) 1990-12-05 1992-03-17 The Boc Group, Inc. Hydrogen and carbon monoxide production by hydrocarbon steam reforming and pressure swing adsorption purification
US5366818A (en) 1991-01-15 1994-11-22 Ballard Power Systems Inc. Solid polymer fuel cell systems incorporating water removal at the anode
FR2672818B1 (en) 1991-02-20 1993-04-23 Air Liquide PROCESS FOR THE PRODUCTION OF OXYGEN BY ADSORPTION.
AU647617B2 (en) 1991-05-09 1994-03-24 Mitsubishi Jukogyo Kabushiki Kaisha Gas separation system and gas recovery system
US5271916A (en) 1991-07-08 1993-12-21 General Motors Corporation Device for staged carbon monoxide oxidation
EP0525521A1 (en) 1991-08-01 1993-02-03 Mitsubishi Jukogyo Kabushiki Kaisha Gas separator system
JPH0779946B2 (en) 1991-09-13 1995-08-30 工業技術院長 Gas adsorption / desorption control method
US5177300A (en) 1991-11-12 1993-01-05 Uop Process for separating naphthalene from substituted benzene hydrocarbons
FR2684023B1 (en) 1991-11-26 1994-01-14 Air Liquide PROCESS FOR PRODUCING A GAS WITH A SUBSTANTIAL OXYGEN CONTENT.
US5227598A (en) 1991-12-23 1993-07-13 General Electric Company In place regeneration of adsorbents using microwaves
GB9207298D0 (en) * 1992-03-31 1992-05-13 Boc Group Plc Treating materials with ozone
FR2689785B1 (en) 1992-04-13 1994-05-20 Air Liquide ROTARY DEVICE FOR SEPARATING BY ADSORPTION OF AT LEAST ONE CONSTITUENT OF A GASEOUS MIXTURE.
US5256172A (en) 1992-04-17 1993-10-26 Keefer Bowie Thermally coupled pressure swing adsorption
WO1994003937A1 (en) 1992-08-10 1994-02-17 Siemens Aktiengesellschaft Fuel cell and electrolyte moistening process
DE4233062A1 (en) * 1992-10-01 1994-04-07 Electrolux Leisure Appliances Sorption apparatus for use in a cooling system
US5330561A (en) 1992-11-16 1994-07-19 Air Products And Chemicals, Inc. Extended vacuum swing adsorption process
DE4318818C2 (en) 1993-06-07 1995-05-04 Daimler Benz Ag Method and device for providing conditioned process air for air-breathing fuel cell systems
US5429665A (en) 1993-10-27 1995-07-04 Botich; Leon A. Apparatus for introducing microwave energy to desiccant for regenerating the same and method for using the same
US5415748A (en) 1994-02-23 1995-05-16 United Technologies Corporation Process for the electrophoretic deposition of defect-free metallic oxide coatings
US5487775A (en) 1994-05-09 1996-01-30 The Boc Group, Inc. Continuous pressure difference driven adsorption process
US5411578A (en) 1994-05-10 1995-05-02 Air Products And Chemicals, Inc. Vacuum swing adsorption process with mixed repressurization and provide product depressurization
US5509956A (en) 1994-07-08 1996-04-23 Horizon Holdings, Inc. Regenerative apparatus for recovery of volatiles
FR2722426B1 (en) 1994-07-18 1996-08-23 Air Liquide PROCESS FOR THE SEPARATION OF NITROGEN FROM A GAS MIXTURE BY ADSORPTION
DE4425913A1 (en) * 1994-07-21 1996-01-25 Hoechst Ag Methods and filters for removing organic matter and ozone from gases
US5531809A (en) 1994-09-14 1996-07-02 Air Products And Chemicals, Inc. Pretreatment layer for CO-VSA
US5593478A (en) 1994-09-28 1997-01-14 Sequal Technologies, Inc. Fluid fractionator
US5900329A (en) 1994-10-19 1999-05-04 Siemens Aktiengesellschaft Fuel-cell system and method for operating a fuel-cell system
US5523326A (en) 1994-10-28 1996-06-04 Uop PSA process with reaction for reversible reactions
GB9422833D0 (en) 1994-11-11 1995-01-04 Secr Defence Pressure and temperature swing absorbtion
US5604047A (en) 1995-06-23 1997-02-18 Exxon Research And Engineering Company Carbon monoxide removal method based on adsorption/steam desorption cycle
US5989314A (en) 1995-09-26 1999-11-23 Praxair Technology, Inc. Pressure swing adsorption air prepurifier
US5656064A (en) 1995-10-04 1997-08-12 Air Products And Chemicals, Inc. Base treated alumina in pressure swing adsorption
JP3554092B2 (en) 1995-10-11 2004-08-11 本田技研工業株式会社 Fuel cell fuel gas supply method
US6045933A (en) 1995-10-11 2000-04-04 Honda Giken Kogyo Kabushiki Kaisha Method of supplying fuel gas to a fuel cell
US5925322A (en) * 1995-10-26 1999-07-20 H Power Corporation Fuel cell or a partial oxidation reactor or a heat engine and an oxygen-enriching device and method therefor
US5656067A (en) 1996-02-23 1997-08-12 Air Products And Chemicals, Inc. VSA adsorption process with energy recovery
US6063161A (en) 1996-04-24 2000-05-16 Sofinoy Societte Financiere D'innovation Inc. Flow regulated pressure swing adsorption system
US5711926A (en) 1996-05-14 1998-01-27 Knaebel; Kent S. Pressure swing adsorption system for ammonia synthesis
US5766311A (en) 1996-07-03 1998-06-16 Praxair Technology, Inc. Multi-thermal pulse PSA system
US5811201A (en) 1996-08-16 1998-09-22 Southern California Edison Company Power generation system utilizing turbine and fuel cell
DE59708082D1 (en) * 1996-10-31 2002-10-02 Ultrafilter Internat Ag ADSORPTION DRYER SYSTEM AND METHOD FOR ITS FUNCTIONAL CHECK
US5827358A (en) 1996-11-08 1998-10-27 Impact Mst, Incorporation Rapid cycle pressure swing adsorption oxygen concentration method and apparatus
US5955039A (en) 1996-12-19 1999-09-21 Siemens Westinghouse Power Corporation Coal gasification and hydrogen production system and method
EP0952883A1 (en) 1996-12-31 1999-11-03 Bowie Gordon Keefer High frequency pressure swing adsorption
DE19701560C2 (en) 1997-01-17 1998-12-24 Dbb Fuel Cell Engines Gmbh Fuel cell system
US6283723B1 (en) 1997-01-27 2001-09-04 Vairex Corporation Integrated compressor expander apparatus
DE19727376C2 (en) 1997-06-27 2002-07-18 Daimler Chrysler Ag Process for the adsorption of organic substances in the air
US6056804A (en) 1997-06-30 2000-05-02 Questor Industries Inc. High frequency rotary pressure swing adsorption apparatus
DE19730292C1 (en) 1997-07-15 1999-03-11 Daimler Benz Ag Plant for the removal of gaseous organic substances from the air
AU752114B2 (en) * 1997-12-01 2002-09-05 Air Products And Chemicals, Inc. Modular pressure swing adsorption apparatus
DE19755116C1 (en) 1997-12-11 1999-03-04 Dbb Fuel Cell Engines Gmbh Method of operating a Proton Exchange Membrane fuel cell system
US6051050A (en) 1997-12-22 2000-04-18 Questor Industries Inc. Modular pressure swing adsorption with energy recovery
US6060032A (en) 1998-07-27 2000-05-09 Air Products And Chemicals, Inc. Layered adsorbent bed for carbon monoxide production
US6921597B2 (en) 1998-09-14 2005-07-26 Questair Technologies Inc. Electrical current generation system
JP3473436B2 (en) 1998-09-16 2003-12-02 株式会社豊田自動織機 Fuel cell device
US6293998B1 (en) * 1998-12-11 2001-09-25 Uop Llc Apparatus for use in pressure and temperature swing adsorption processes
US6398853B1 (en) 1998-12-16 2002-06-04 Quest Air Gases Inc. Gas separation with split stream centrifugal turbomachinery
US6143057A (en) 1999-04-23 2000-11-07 The Boc Group, Inc. Adsorbents and adsorptive separation process
AU5381200A (en) 1999-06-09 2001-01-02 Questair Technologies, Inc. Rotary pressure swing adsorption apparatus
US6190623B1 (en) 1999-06-18 2001-02-20 Uop Llc Apparatus for providing a pure hydrogen stream for use with fuel cells
US6231644B1 (en) 1999-07-23 2001-05-15 The Boc Group, Inc. Air separation using monolith adsorbent bed
US6514319B2 (en) * 1999-12-09 2003-02-04 Questair Technologies Inc. Life support oxygen concentrator
BE1013441A3 (en) * 2000-05-17 2002-01-15 Atlas Copco Airpower Nv COMPRESSOR INSTALLATION WITH A heatless and ADSORPTION DRYER therefor.
WO2002035623A2 (en) 2000-10-27 2002-05-02 Questair Technologies Inc. Systems and processes for providing hydrogen to fuel cells
US6770390B2 (en) * 2000-11-13 2004-08-03 Air Products And Chemicals, Inc. Carbon monoxide/water removal from fuel cell feed gas

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008089563A1 (en) * 2007-01-24 2008-07-31 Xebec Adsorption Inc. Guard layers for rapid cycle pressure swing adsorption devices
US8303683B2 (en) 2007-01-24 2012-11-06 Air Products And Chemicals, Inc. Guard layers for rapid cycle pressure swing adsorption devices
CN114931845A (en) * 2021-12-31 2022-08-23 安徽华塑股份有限公司 Industrial hydrous hydrogen chloride gas dehydration equipment

Also Published As

Publication number Publication date
US20020134246A1 (en) 2002-09-26
WO2002047797A1 (en) 2002-06-20
EP1355717A1 (en) 2003-10-29
JP2004515349A (en) 2004-05-27
US20040261618A1 (en) 2004-12-30
EP1355717A4 (en) 2006-10-25
US7160367B2 (en) 2007-01-09
CN1479646A (en) 2004-03-03
AU2002230897A1 (en) 2002-06-24
CN100371051C (en) 2008-02-27
US7037358B2 (en) 2006-05-02

Similar Documents

Publication Publication Date Title
CA2329475A1 (en) Fast cycle psa with adsorbents sensitive to atmospheric humidity
US6488747B1 (en) Pressure swing adsorption with axial or centrifugal compression machinery
US6514318B2 (en) Multistage system for separating gas by adsorption
US4452612A (en) Separation and purification of gases and vapors by continuous pressure-swing adsorption
US6406523B1 (en) Rotary pressure swing adsorption apparatus
KR100346487B1 (en) Pressure swing adsorption gas flow control method and system
US6231644B1 (en) Air separation using monolith adsorbent bed
KR100346488B1 (en) Single bed pressure swing adsorption process and system
JP4708562B2 (en) Module pressure swing absorber
US6051050A (en) Modular pressure swing adsorption with energy recovery
JP5497251B2 (en) Layer manifold pressure swing adsorption device and adsorption method
US5766311A (en) Multi-thermal pulse PSA system
US5948142A (en) Pressure and temperature swing adsorption and temperature swing adsorption
CA2366266A1 (en) Argon purification process
US20230211276A1 (en) Method for capture of carbon dioxide from ambient air and corresponding adsorber structures with a plurality of parallel surfaces
WO2011123210A1 (en) Contaminant mitigation in psa air fractionation
CA2430156C (en) Psa with adsorbents sensitive to contaminants
KR102473002B1 (en) Method and apparatus for compressing and drying a gas
EP0880903B2 (en) Method for treating the atmosphere contained in enclosed spaces
CA2274286A1 (en) Rotary pressure swing adsorption apparatus
CA2374536C (en) Multistage system for separating gas by adsorption
CA2374292A1 (en) Rotary pressure swing adsorption apparatus
WO2002030547A2 (en) Multiple plate sorption assembly and method for using same

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued