WO2001096013A1 - Method and reactivating solid catalysts used in alkylation reactions - Google Patents
Method and reactivating solid catalysts used in alkylation reactions Download PDFInfo
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- WO2001096013A1 WO2001096013A1 PCT/US2001/019096 US0119096W WO0196013A1 WO 2001096013 A1 WO2001096013 A1 WO 2001096013A1 US 0119096 W US0119096 W US 0119096W WO 0196013 A1 WO0196013 A1 WO 0196013A1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J38/48—Liquid treating or treating in liquid phase, e.g. dissolved or suspended
- B01J38/50—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using organic liquids
- B01J38/56—Hydrocarbons
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J2038/005—Regeneration or reactivation of catalysts, in general involving supercritical treatment
Definitions
- This invention relates to catalyst reactivation methods. More particularly, this invention relates to methods for reactivating totally or partially deactivated alkylation catalysts with a reactive near-critical, critical or supercritical fluid reactivating agent.
- alkanes As conventionally accepted in the literature on alkylation, terms such as alkanes, paraffins and paraffinic hydrocarbons will hereinafter refer to open-chain saturated hydrocarbons.
- the suffix -ene is adopted for straight-chain monounsaturated hydrocarbons, so that a term such as butene refers to at least one ofthe compounds 1 - butene and 2-butene.
- the suffix -ylene is hereinafter employed to refer to a monounsaturated hydrocarbon that consists of the same number of carbon atoms as expressed by the name.
- the term butylene refers to at least one of the compounds 1 -butene, 2-butene, and isobutylene, the latter compound also is known as 2-methylpropene.
- alkenes, olefins and olefinic hydrocarbons generically refer to monounsaturated hydrocarbons.
- the prefix iso- is generically used to refer to branched alkanes or alkenes that have one or more methyl groups only as side chains.
- Aromatic hydrocarbons refer to hydrocarbons that have at least one aromatic ring and to hydrocarbons which, although strictly not aromatic, contain conjugation to the extent such that they undergo alkylation reactions like aromatic compounds.
- C n describes a hydrocarbon with n carbon atoms, whether the hydrocarbon is linear, branched, paraffinic, olefmic or aromatic.
- the notation C n - C m describes at least one hydrocarbon in the set of hydrocarbons such that the number of carbon atoms ranges from n to m for any individual hydrocarbon in the set.
- the notation C n ⁇ p or C p+ refers to at, least one hydrocarbon with at least p carbon atoms, and it often refers to a mixture of hydrocarbons such that the number of carbon atoms is at least p for any individual hydrocarbon in the mixture.
- alkylation generically refers to the addition of an alkyl group to a molecule that is to be alkylated.
- Alkylation of alkenes to produce alkylation products, or alkylate is an addition of a saturated hydrocarbon (R-H) to an alkene to yield a saturated hydrocarbon of higher molar mass.
- R-H saturated hydrocarbon
- Alkyl ation is extensively used in the petroleum industry to produce medium- or large- mass hydrocarbons from smaller molecules.
- One ofthe more important alkylation reactions is the addition of isobutane to 2 : butene to produce 2,2,4-trimethylpentane according to the following equation:
- Equation (1) is an alkane, paraffin or paraffinic hydrocarbon
- the second reactant in the same equation is an alkene, olefin, or olefinic hydrocarbon that can also correspond in that equation with an alkylene.
- the paraffin which is listed as the first reactant in equation (2) is isobutane
- the alkylene which is listed as the second reactant in the same equation is 2-butene.
- equations (1) and (2) describe with varying degrees of generality paraffin alkylation, or the addition reaction of a paraffin and an olefin. Equation (2), in particular, describes the addition reaction of an isoparaffin and an olefin where the alkylate is an isoalkane.
- Equation (1) describes a reaction that includes, for example, the reaction of a C 4 - C 8 paraffinic hydrocarbon with a C 2 - Cj 2 olefinic hydrocarbon to produce a branched paraffinic hydrocarbon.
- a C 4 isoparaffin reacts with a C 4 olefin to produce a C 8 isoparaffin.
- aromatic hydrocarbons can also be alkylated.
- benzene can be alkylated with ethylene to produce ethylbenzene, a precursor of styrene, according to the zeolite catalyzed reaction that is described by equation (3):
- Ethylbenzene yields, upon dehydrogenation, styrene, which is the simplest and most important member of a series of unsaturated aromatic compounds.
- the zeolite-catalyzed alkylation of benzene by ethylene has been described in a number of sources. See, for example, Kirk-Othmer Encyclopedia of Chemical Technology, Nol.21 , pp .770- 800, 3rd ed. (1983).
- the olefins in equations (l)-(3) are the respective alkylating agents.
- the amount ofthe reactant to be alkylated exceeds the amount of the alkylating agent.
- the paraffin-to-olefin molar ratio exceeds 3:1. However, ratios as high as 100: 1 can be employed.
- the use of a large-pore zeolite with a Lewis acid reportedly increases the activity and selectivity of the zeolite, thus permitting effective alkylation at high olefin weight hour space velocity (OWHSN) and low isoparaffin/olefin ratio.
- OWHSN is defined as the amount of olefin fed to the reactor per unit catalyst per hour (i.e., g olefin (g catalyst) "1 h "1 ).
- the principal industrial application of paraffin alkylation is in the production of premium-quality fuels for internal combustion engines. More specifically, alkylation is mainly used to provide a high octane blending alkylate for automotive fuels that also increases the fuel sensitivity to octane-enhancing agents. Alkylate components are typically characterized by clean, low emission burning. Because of these properties, alkylate production capacity is expected to increase as specifications for gasoline become more stringent.
- Catalysts used in industrial alkylations have typically been strong liquid acids, such as sulfuric acid and hydrofluoric acid.
- Other strong acids have been used in laboratory or industrial alkylations. These acids include aluminum trichloride, and super acids such as trifluoromethanesulfonic acid.
- liquid acid alkylation requires the use of a fairly concentrated acid and the replacement of consumed acid.
- sulfuric acid concentration is controlled above 90% to provide optimum activity and selectivity, and hydrofluoric acid concentration is maintained in the range of 85-95%.
- These acids are recognized hazardous materials, whose use requires the adoption of periodic hazard reviews of the operating units and the implementation of safety procedures and measures to minimize the probability of accidental releases.
- Other typically costly measures that must be adopted include control operations to mitigate the detrimental effects of such possible accidents.
- Red oil is another product derived form liquid acid catalysis that presents disposal and recycling problems.
- Red oil is predominantly the conjugation product of an acid and alkylate that has to be disposed of, or recycled. Disposal presents a problem that is inherent in the storage, handling and deposit of hazardous substances. Further, recycling is also an expensive operation because it requires the implementation of additional processes that significantly increase the cost of producing the desired alkylate.
- liquid acid alkylation catalysts cause technological developments in alkylations to be greatly influenced by environmental considerations.
- One, reason is that modern low emission gasoline formulations rely heavily on alkylate.
- liquid acid alkylation catalysts requires a constant improvement of process safety, the reduction of waste disposal, and the limitation ofthe environmental consequences of any process emissions.
- liquid acid catalysis employing sulfuric acid or hydrofluoric acid is not an effective means for catalyzing certain alkylations, such as the alkylation of benzene with ethylene.
- alkylation catalysts which can be used in the production of low emission fuels, which are noncorrosive and easy to handle, and which can be effectively reactivated to avoid disposal problems.
- solid acid catalysts are easier to handle and less hazardous than liquid acid catalysts, they are good candidates to replace liquid acid alkylation catalysts.
- solid catalysts are known to deactivate relatively rapidly as a consequence of fouling of the active sites by heavy reaction intermediate products and byproducts. This is considered a major hurdle for the effective.use of solid acid alkylation catalysis. See Kirk-Othmer, Encyclopedia of Chemical Technology, Nol.2, ⁇ .92, 4th ed. (1991). Rapid deactivation of solid acid catalysts leads to relatively large volumes of material that must be discarded.
- catalysf'as used herein includes any solid catalyst with sufficient strength to carry out alkylations.
- alkylation catalysts including molecular sieves, and in particular zeolites, silicates, aluminophosphates, and silicoaluminqphosphates.
- Alkylation catalysts can be chosen from among a variety of substances, with the specific catalyst often determined by the character of the processes carried out in the plant where the alkylation takes place.
- Zeolites which can be natural, synthetic or mixtures thereof used as catalysts in alkylations include ZSM-4, ZSM-3, ZSM-5, ZSM-20, ZSM-18, ZSM-12, ZSM- 35, ZSM-48, ZSM-50, MCM-22, PSH-3, TMA offretite, TEA mordenite, REY, faujasites comprising zeolite Y and mordenite, ultrastable Y zeolites (USY), and a number of zeolites such as zeolite beta, zeolite Omega, zeolite L, and clinoptilolite, and rare-earth metal containing forms of zeolites.
- catalysts include at least one among a variety of inorganic oxides such as alumina, and in particular ⁇ or ⁇ alumina, silica, boria, phosphorous oxides, titanium dioxide, zirconium dioxide, chromia, zinc oxide, magnesia, calcium oxide, silica-alumina, silica-magnesia, silica- alumina-magnesia, silica-alumina-zirconia, sulfated mixed-metal oxides, and more generally a variety of refractory inorganic oxides and natural substances such as bauxite, clay, including kaolin andbentonite, and diatomaceous earth.
- inorganic oxides such as alumina, and in particular ⁇ or ⁇ alumina, silica, boria, phosphorous oxides, titanium dioxide, zirconium dioxide, chromia, zinc oxide, magnesia, calcium oxide, silica-alumina, silica-magnesi
- Molecular sieves that also catalyze alkylations include pillared silicates and/or clays, aluminophosphates such as ALPO-5 and NPI-5; silicoaluminophosphates such as SAPO-5, SAPO-37, SAPO-3 1, SAPO-40, and SAPO-41, other metal aluminophosphates, and layered materials such as MCM-36. These catalysts, alone or in combination among themselves or with other substances are known to be used in alkylations of olefins and aromatic hydrocarbons.
- one ofthe non- zeolitic substances that can be combined with zeolites in the preparation of alkylation.catalysts is at least one Lewis acid, such as boron trifluoride, antimony pentafluoride, and aluminum trichloride.
- Refractory oxides can be used in combination with other catalytic substances to provide temperature resistance.
- diluent materials such as various oxides and clays can be incorporated to control the conversion rate, to improve the catalyst's mechanical properties, to provide a matrix material, and/or to act as catalyst binders.
- Other active substances for example platinum and/or palladium, can also be incorporated into alkylation catalysts to provide a metal hydrogenation function.
- Other catalysts capable of catalyzing alkylation can be produced by the deposition of agents covalently bound to, or entrained in, polymers on a solid surface not generally capable or poorly capable of catalyzing alkylation.
- an alkylation catalyst does not effectively modify alkylation kinetics when the catalyst is under conditions such that not all ofthe alkylation reactants are available. Conditions in which not all ofthe alkylation reactants are present for the alkylation to take place will hereinafter be referred to as "the absence of alkylation.”
- Reactants, intermediate reaction species, and alkylates of a variety of sizes and shapes can participate in a variety of alkylations.
- the shape and size selectivity ofthe zeolite is directly related to the shape and size ofthe channels in the zeolite. Accordingly, selection of the appropriate zeolite for any given alkylation will be determined by its structural characteristics. Structure, dimensions and pore characteristics of zeolites are provided in numerous sources, such as J.A. Martens, et al., Estimation of the void structure and pore dimensions of molecular sieve zeolites using the hydroconversion of n-decane, Zeolites 4, 98 (1984); W.
- zeolite A, erionite, and chabazite are classified as small-pore zeolites; medium-pore zeolites include zeolites ZSM-5, ZSM-1 1, ZSM-22, ZSM-23, ZSM-48, NU-10, Theta 1, TS-1, and sihealite; and large-pore zeolites comprise faujasite, X-zeolite, Y-zeolite, mordenite, offretite, zeolite L, zeolite Omega, zeolites ZSM-4, ZSM-12, and zeolite Z.
- U.S. Patent Nos. 4,605,811 (hereinafter the '"811 patent”) and 4,721,826 (hereinafter the '"826 patent”) disclose a process for restoring or maintaining the activity of heterogeneous catalysts for reactions at normal and low pressures. Catalyst activity is restored or maintained by using a pressure greater than the critical pressure of the fluid phase and a temperature higher than or equal to the critical temperature of the fluid phase.
- the process disclosed in these patents includes the reactivation ofthe catalyst at a pressure and temperature that are in the supercritical region ofthe reaction medium phase diagram.
- the alkylation conversion conditions of this process include temperature and pressure that are, respectively, at least equal to the critical temperature and critical pressure of the component of highest concentration in the feed stock. These conditions are maintained over the entire course of the reaction until the catalyst is completely deactivated.
- the '698 patent does not disclose how to regenerate a completely deactivated catalyst.
- the isoparaffin containing feed is not to be contacted with the catalyst according. to + the process disclosed in the '698 patent underpressure and temperature conditions below the critical temperature and critical pressure ofthe isoparaffin component of highest concentration in the feed.
- U.S. Patent No. 5,310,713 discloses a process for regeneration of an alkylation catalyst with hydrogen. This process requires reactivation with hydrogen gas that can be mixed with liquid isobutane as a solvent.
- U.S. Patent No . 5 ,491 ,277 (hereinafter the '"277 patent") discloses a mixed-phase solid bed hydrocarbon alkylation process where "the exact manner of regeneration does not form ...
- U.S. Patent No. 5,489,732 discloses a fluidized solid bed motor fuel alkylation process in which the solid acid catalyst is continuously regenerated by removing it from the reactor and contacting it with hydrogen.
- the hydrogen is dissolved in feed hydrocarbon and the catalyst is mildly regenerated.
- the catalyst is separated from the liquid phase and regenerated with gaseous hydrogen at a temperature in the range 80-500°C (preferably 100-250°C). The regenerated catalyst is then fluidized with 38°C isobutane and reintroduced to the bottom ofthe reactor.
- the average residence time ofthe regenerating catalyst in the liquid-phase hydrocarbon zone is 0.5-15 min, and the temperature and pressure in this zone are very near the reaction conditions for the alkylation.
- Catalyst reactivation will hereinafter be used to encompass catalyst regeneration and also catalyst reactivation. Catalyst reactivation refers to the treatment of a catalyst that renders it into a form in which it is suitable for its efficient use or re-use as a catalyst. "Reactivating agent” will hereinafter refer to a substance or mixture of substances that is used in catalyst reactivation.
- Fouling substances that are generated in the alkylation process or that are introduced with the feed in the alkylation process fairly quickly reduce the number ofthe catalyst's active sites. Catalytic site reduction leads in turn to a reduction of the alkylation efficiency to a point such that the alkylation no longer takes place to any significant extent.
- Deactivated catalyst disposal would impose heavy burdens, such as those associated with waste disposal regulation compliance and the costs of resupplying the spent catalyst.
- Methods employing supercritical fluids that are directed to the extension of the useful life of catalysts have not addressed the need to reactivate catalysts that have become deactivated.
- proposed methods for prolonging the longevity of alkylation catalysts rely on the maintenance of supercritical temperature and pressure conditions throughout the alkylation.
- the temperature and pressure of alkylation conditions must be within narrow limits to procure the optimal thermodynamic and kinetic conditions and to avoid undesired byproducts and additional fouling agents.
- the choices for the reactivating agent are typically very limited.
- only a very reduced number of substances that do not actually participate in the alkylation itself may have a critical pressure and a critical temperature that fall within the optimal pressure and temperature reaction conditions.
- the alkylation is run at a temperature and pressure high enough that they are within the supercritical conditions of at least one of the reactants.
- This reactant is then assigned the function of removing fouling agents and thus prolonging the longevity ofthe catalyst as an effective alkylation catalyst.
- the required critical pressure and critical temperature might be so high that they are detrimental to the alkylate quality.
- such temperature and/or pressure conditions may favor undesirable side reactions, such as isomerizations, product cracking, olefin oligomerization, and coking, which might predominate over the desired alkylation.
- Product quality and high octane product yield are then significantly reduced.
- some of the undesired side reactions might contribute to the additional build up of fouling agents, thus aggravating the problem that was to be solved.
- the alkylation catalyst is transferred out ofthe reactor for its total or partial reactivation. Reactivation is then accomplished by processes such as calcination, treatment with solvents, and elution with substances that dissolve and/or react with the fouling agents.
- the implementation of this strategy requires the substantial modification of reactor equipment or the complete removal and replacement of catalyst batches.
- An obj ect ofthe invention is to provide methods and systems for reactivating solid alkylation catalysts.
- a further obj ect ofthe invention is to provide methods and systems in which solid alkylation catalyst reactivation occurs whether the catalyst is partially or completely deactivated.
- a method for solid alkylation catalyst reactivation that comprises contacting a catalyst that is partially or even completely deactivated with a fluid reactivating agent.
- This contacting is performed under pressure and temperature conditions such that the fluid reactivating agent is in the form of a dense fluid under any one of a variety of conditions, including near- critical, critical and supercritical conditions.
- Solvent properties facilitate the surface removal of fouling agents and the products of any reaction between the reactivating agent and the fouling agents, which in turn leads to an efficient and fast reactivation process.
- Transport properties facilitate the diffusion of fouling compounds out of the catalyst, thus improving the rate and extent of regeneration.
- One ofthe features ofthe fluid reactivating agent used in the methods of this invention is that it can react with the fouling agents and dissolve some fouling agents as well as the products ofthe reaction between the fluid reactivating agent and fouling agents.
- An advantage of this feature is that it permits faster and more complete catalyst reactivation because of the more intense removal of catalyst fouling agents.
- the methods of this invention are effectively implemented to reactivate a solid catalyst, whether the catalyst is within or outside the alkylation reactor.
- This feature advantageously enhances the versatility of the methods of the present invention because they can be implemented in a great variety of alkylation reactors.
- the ability to reactivate a solid catalyst inside the alkylation reactor advantageously diminishes the duration and complexity of catalyst reactivation.
- Solid catalysts can be reactivated according to this invention under a variety of conditions, which may or may not be close to the alkylation conditions. This feature further enhances the versatility of the methods of the present invention because solid catalyst reactivation can be accomplished without imposing constraints that could be detrimental to the optimal thermodynamic and/or kinetic alkylation conditions.
- the fluid reactivating agent can be chosen to be one ofthe alkylation reactants. This feature advantageously renders solid catalyst reactivation according to this invention relatively simple and cost effective. The simplicity is derived from the fact that a minimal number of chemical species are required for alkylation and catalyst reactivation. Cost effectiveness derives from the reduced physical conditions and technical demands of a catalyst reactivation process which does not require chemical species in addition to those used in the alkylation process.
- the fluid reactivating agent can be , optionally recovered and recycled after catalyst regeneration so as to be incorporated into the alkylation reactant feed and/or into the fresh reactivating agent flow.
- the recovered fluid reactivating agent can be used directly with olefin addition in the alkylation feed stream, or recycled back to the inlet stream ofthe reactivating catalyst reactor, in each case reducing the amount of reactivating agent needed.
- This feature advantageously increases the cost effectiveness of catalyst reactivation according to the invention because of the derived savings in materials.
- the catalyst reactivation methods ofthe invention provide the advantage that deactivated catalysts do not have to be immediately disposed of, but can instead be used in a plurality of catalytic cycles.
- Figure lA schematically shows an embodiment of a two-column system in which the catalyst in reactor 2 is reactivated whereas alkylation takes place in reactor 1.
- Figure IB schematically shows an embodiment of a two-column system in which the catalyst in reactor 1 is reactivated whereas alkylation takes place in reactor 2.
- Figure 2 schematically shows relevant features of a one-component system P-T phase diagram.
- Figure 3 shows a production rate vs. time diagram for an example reactivation run with isobutane as the regenerant, at 150 °C, 1600 psig, 2 hours, and 33 g isobutane (g catalyst) "1 h "1 .
- Figure 4 shows a diagram of process conditions over the course ofthe run for an example reactivation run with isobutane as the regenerant, at 180 °C, 1600 psig, 2 hours, and 33 g isobutane (g catalyst)" 1 h "1 .
- FIG. 5 shows a diagram of feed composition data as a function of time for the example reactivation run with isobutane as the regenerant, at 180 °C, 1600 psig, 2 hours, & 33 g isobutane (g catalyst) "1 h "1 .
- Figure 6 diagrammatically shows the effect of the temperature on the percentage of recoverable trimethylpentane (TMP) production with isobutane as the regenerant, at 1600 psig, 2 hours, and 33 g isobutane (g catalyst)" 1 h" 1 .
- TMP trimethylpentane
- FIG. 7 shows the effect ofthe pressure on the percentage of recoverable trimethylpentane (TMP) production with isobutane as the regenerant, at 150 °C, 2 hours, and 33 g isobutane (g catalyst) "1 h "1 .
- Figure 8 shows the effect of temperature on the percentage of recoverable trimethylpentane (TMP) production with isobutane as the regenerant, at a constant isobutane density of 0.41 g/mL, 2 hours, and 33 g isobutane (g catalyst) "1 h" 1 .
- Figure 9 shows total alkylate (C5+) and trimethylpentanes (TMP) product yields for a multiple reactivation experiment with reaction at 60 °C, 1600 psig, an
- Figure 10 shows the variation of run time (time to drop to 95% butene conversion) with each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 !- '1 .
- Figure 11 shows the change in percentage of recovered alkylate (C5+) and trimethylpentane (TMP) production with each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an
- Figure 12 shows total alkylate (C5+) and trimethylpentane (TMP) yields in each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h "1 .
- Figure 13 shows the variation of cumulative alkylate (C5+) and trimethylpentane (TMP) yields with run number for the complete multiple reactivation experiment in the reactor at an OWHSV of 0.2 g trans-2 -butene (g catalyst)" 1 h” 1 .
- Figure 14 shows the cumulative run time with run number for the complete multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans- 2-butene (g catalyst) "1 h "1 .
- Figure 15 shows total alkylate (C5+) and trimethylpentanes (TMP) product yields for a multiple reactivation experiment with reaction at 60 °C, 1600 psig, an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h “1 , inlet isobutane: trans-2-butene molar ratio of 20:1, in the plug flow reactor with recycle.
- the recycle ratio was 12:1.
- Reactivation was at 180 °C, 1600 psig, for 2 hours, with 33 g isobutane (g catalyst) "1 h "1 .
- the reactivation criterion was alkylation run time of exactly 3 hours.
- Figure 16 shows the run times (exactly 3 h per alkylation run) with each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst)" 1 h" 1 .
- Figure 17 shows the change in percentage of recovered alkylate (C5+) and trimethylpentane (TMP) production with each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h "1 , with 3 h of alkylation as the reactivation criterion. Values are compared with the initial run (100%).
- Figure 18 shows total alkylate (C5+) and trimethylpentane (TMP) yields in each successive run (after being reactivated) for the multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst)" 1 h" 1 , with 3 h of alkylation as the reactivation criterion.
- Figure 19 shows the variation of cumulative alkylate (C5+) and trimethylpentane (TMP) yields with run number for the complete multiple reactivation experiment in the reactor at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h "1 , with 3 h of alkylation as the reactivation criterion.
- Figure 20 shows the cumulative run time with run number for the complete multiple reactivation experiment in the recycle reactor at an OWHSV of 0.2 g trans- 2-butene (g catalyst) "1 h "1 , with 3 h of alkylation as the reactivation criterion.
- the present invention is directed to methods and systems for reactivating a partially or totally deactivated solid alkylation catalyst in such a way that the optimal pressure and temperature of alkylation conditions do not have to be altered to accommodate the reactivation process.
- the catalyst may be kept within the alkylation reactor during both the alkylation and reactivation processes, or may be removed for the reactivation, depending on the particular piping and mechanical configuration employed.
- Catalyst reactivation according to this invention is accomplished by contacting the partially or totally deactivated catalyst with a fluid reactivating agent that can dissolve the fouling agents that deactivate the catalyst.
- the reactivating ability ofthe fluid reactivating agent of this invention is enhanced because the fluid reactivating agent is chosen so that it reacts with the fouling agents that deactivate the catalyst in a way that enhances desorption ofthe fouling agent from the catalyst surface, at or away from the reactive site. Removal of the reactivating fluid with the fouling agents and products ofthe reaction ofthe fluid reactivating agent with the fouling agents leads to a reactivated catalyst that can effectively be reused in subsequent alkylations.
- reactivation methods according to the present invention do not interfere with the alkylation itself.
- reactivation is performed while no alkylation takes place in the reactor that contains at least a partially deactivated catalyst.
- the reactivation is performed while the catalyst is outside the reactor compartment in which alkylation takes place. Reactivation of the catalyst outside the alkylation reactor is performed analogously as reactivation is carried out when the catalyst is within the alkylation reactor. However, reactivation of the catalyst outside the reactor involves the additional operations of removing the catalyst from and reinserting it into the reactor.
- Reactivation of the catalyst in the reactor while no alkylation takes place is preferably accomplished according to this invention with a swing column system that permits the controlled and independent direction of the flow of alkylation reactants and the flow of fluid reactivating agent.
- a schematic depiction of a swing column system 10 is shown in Figures lA-lB.
- FIGs in Figures 1A-1B show reactors 1 and 2 which are embodied by any model of suitable alkylation reactors.
- the reactors ⁇ and 2 are an example of means for holding at least one solid alkylation catalyst. It will be understood by those skilled in the art that a variety of reactor configurations may be utilized to accomplish this function.
- Active flow lines in the embodiments sketched in Figures 1A-1B are represented by the thicker arrows . These active flow lines comprise lines 12, 14, 16, 18, and 20 in Figure 1A, and lines 32, 34, 36, 38, and 20 in Figure IB. Closed lines through which no flow is intended to circulate are represented in Figures 1A-1B by thinner lines. These closed lines comprise lines 11, 13, 15, and 17 in Figure lA, and lines 33, 35, 37, and 39 in Figure IB.
- Feed mix 25 comprises the alkylation reactants. This feed mix is supplied in the embodiment shown in Figure 1A ,to one reactor whereas fluid reactivating agent 27 is supplied to another reactor, which contains at least partially deactivated alkylation catalyst.
- feed mix 25 is supplied to reactor 1 whereas fluid reactivating agent 27 is supplied to reactor 2.
- Catalyst in reactor 1 is active enough as to be able to effectively catalyze alkylation with feed mix 25 supplied through active flow 12. The alkylate obtained thereby is transported by active flow 16 to downstream processing 29.
- Fluid reactivating agent 27 is supplied through active flow line 14 in the embodiment shown in Figure 1A to reactor 2 which contains at least partially deactivated alkylation catalyst.
- the active flow line 14 with associated pumping devices is an example of means for directing a fluid reactivating agent toward the catalyst. It will be understood by those skilled in the art that a variety of configurations and devices may be utilized to accomplish this function.
- the catalyst is reactivated by the fluid reactivating agent which dissolves the fouling agents deposited in the catalyst and also reacts with some fouling agents to enhance the reactivation.
- a means for generating pressure and temperature conditions while the catalyst is in contact .with the fluid reactivating agent in the absence of alkylation is provided such that the fluid reactivating agent is dense enough to dissolve impurities and is a near-critical gas or near-critical liquid, or is at or above the critical point. It will be understood by those skilled in the art that a variety of pressure and temperature control devices can be utilized to generate the optimum pressure and temperature conditions during catalyst regeneration.
- the fluid reactivating agent, along with dissolved fouling agents and the products of the reaction of the fluid reactivating agent with fouling agents, are transported through line 18 to fluid reactivating agent recovery processing with the option of recirculating such flow through line 20 back into reactor 2.
- the reactivating conditions in reactor 2 can be chosen to optimize the reactivation process without interfering with the actual alkylation that takes place in reactor 1 and in any other additional reactor (not shown in Figure lA).
- Catalyst reactivation according to this embodiment can be performed at any desired stage in any cycle of the catalyst's performance. For example, alkylation can be run in reactor 2 until the catalyst contained therein is completely deactivated, or it can be run only up to the stage where the catalyst is deactivated to a determined extent.
- the number of reactors in the swing column system is chosen according to the relative duration of each of the alkylation and reactivation processes in the different reactors. For example, when catalyst reactivation is completed before the alkylation catalyst has become deactivated to an unacceptable extent, a plurality of alkylation reactors can be maintained in the swing column system while the catalyst in only a single reactor is being reactivated.
- the alkylation reaction and reactivation process ofthe present invention can take place at the same pressure.
- Alkylation can take place at lower temperatures where the highly branched trimethylpentane products are favored.
- the temperature can be increased to optimize the removal of catalyst fouling agents. Reducing pressure swings simplifies flow processes, improves reliability, and reduces operating costs of a commercial unit.
- the methods of this invention can be used to reactivate an alkylation catalyst regardless of the reactor type that is used for the actual alkylation process.
- the methods of this invention can effectively be used to reactivate alkylation catalysts in conjunction with a variety of other reactor types as well.
- reactor types include, but are not necessarily limited to, packed bed systems, and systems where the catalyst is physically moved through alkylation and reactivation zones within a single reactor or among several separate reactors, such as in continuous stirred tank reactors (CSTR).
- CSTR continuous stirred tank reactors
- one reactor can provide a reactivation zone for catalyst regeneration and another reactor can provide an alkylation zone for performing alkylation reactions, with the catalyst physically moved therebetween.
- the methods of this invention could be implemented in conjunction with partial or total recycle of the reactivating reactor effluent to the reactor inlet.
- catalyst fouling agents include long chain hydrocarbons which have low volatility and high molar mass. Because of their low volatility, these fouling agents do not evaporate easily. Furthermore, these fouling agents diffuse poorly through the catalyst's pores because of their high molar mass.
- the mechanism whereby the fluid reactivating agent of this invention effectively removes fouling agents from the catalyst is most likely complex.
- the fluid reactivating agent may remove fouling agents according to this invention by a process that includes the reactive release of the fouling agents from the catalyst. It is believed that fouling agents are deposited at the catalyst's active sites in the form of carbocations that interact with the catalyst's active sites.
- a fluid reactivating agent such as isobutane may lead to hydride transfer to the high molecular weight carbocation and its subsequent release from the catalyst active sites.
- the isobutane in turn forms a C 4 -carbocation with the catalyst active site, activating the catalyst active site for subsequent alkylation once olefin is reintroduced to the reactor.
- This activation of the active site eliminates the induction period commonly seen with fresh alkylation catalyst, thus increasing the initial rate of the alkylation reactions.
- the reactive aspect ofthe reactivating function performed by embodiments ofthe fluid reactivating agent of this invention is consistent with the results obtained from reactivation with He, and independently with n-pentane. Less than 35% ofthe completely deactivated catalyst's activity is recovered in these reactivation processes. These percentages of recovery of less than 35% are believed to be due to high temperature cracking and volatilization or solubilization ofthe fouling agents by the fluid reactivating agent, such as He or n-pentane. In contrast, up to 83% of the completely deactivated catalyst's activity can be recovered with a fluid reactivating agent according to this invention, such as supercritical isobutane. These results indicate that mere cracking and subsequent volatilization or dissolution ofthe fouling agents do not lead to the high reactivation effects achieved by embodiments ofthe present invention.
- Some conventional processes for treating catalysts rely on an initial washing of the deactivated catalyst with liquid isobutane, and subsequently these processes rely on a gas such as hydrogen, typically in the presence of at least one metal such as Pt, Pd, and Ni, to reactivate the catalyst.
- Isobutane is an embodiment of a fluid reactivating agent according to the present invention, and it is relied on for the primary reactivating function.
- a fluid reactivating agent according to this invention can optionally be mixed with at least one gas, such as hydrogen or oxygen, because the fluid reactivating agent under supercritical conditions dissolves such gas. The added gas or a mixture thereof supplements then the reactivating effects of the fluid reactivating agent of this invention.
- Embodiments of this invention that include a gas dissolved in the fluid reactivating agent are preferably used in the presence of at least a metal such as Pt, Pd, and Ni.
- FIG. 2 schematically shows a one-component system phase diagram that is used hereinbelow to describe the pressure and temperature conditions for the catalyst reactivation methods according to this invention. It is understood that the phase diagram shown in Figure 2 is merely a sketch representing qualitatively basic features of a phase diagram of a one- component system. This diagram is merely used for the purpose of introducing the terminology that will be adopted hereinbelow to characterize the pressure and temperature conditions at which the catalyst reactivation is performed according to the present invention.
- Lines 3, 4 and 5 in the pressure (P) - temperature (T) diagram sketched in Figure 2 represent respectively the solid-liquid, solid-gas and liquid-gas equilibrium lines.
- Point 7 is called the triple point and point 6 is called the critical point, which is defined by a critical pressure (P c ) and by a critical temperature (T c ).
- the region to the right ofthe solid-liquid equilibrium line 3 and above the liquid-gas equilibrium line 5 for temperatures less than T c represents states ofthe fluid system which is in the liquid phase (l).
- the region to the right ofthe solid-gas equilibrium line 4 and below the liquid-gas equilibrium line 5 for temperatures below T c represents states ofthe fluid system which is in the gas phase (g).
- the region to the left ofthe solid-gas equilibrium line 4 and to the left ofthe sohd-liquid equilibrium line 3 represents states of the. system which is in a solid phase (s).
- the region for temperatures greater than T c and pressures greater than P c represents states ofthe fluid system that are supercritical.
- NC liquid is used herein to refer to all pressures corresponding to a liquid phase in the temperature range of about 0.9 - 1 T c , where T c is referred to on an absolute temperature scale such as degrees Kelvin (K) or degrees Rankine (°R).
- K degrees Kelvin
- °R degrees Rankine
- critical is used herein to characterize a pressure and a temperature that are equal to P c and T c , respectively.
- supercritical is used herein to refer to a pressure and a temperature which are greater than P c and T c , respectively, and "SCF" is used as an acronym for "supercritical fluid".
- SCF supercritical fluid
- Characteristics of a supercritical fluid include transport properties that are more similar to those of a gas and density that is more similar to that of a liquid.
- a supercritical fluid typically has a viscosity that is closer to that of a gas than to the liquid viscosity. High density is a desirable property when the fluid is utilized for dissolving other substances.
- the near-critical (NC) gas region ofthe phase diagram that is of interest in the context of this invention is the range of pressures and temperatures for a fluid which is dense enough as to effectively dissolve and/or transport catalyst fouling agents and the products of any reaction of the fluid reactivating agent with catalyst fouling agents, where an NC gas is defined as the fluid existing in its gas phase in the range of about 0.1 - 1 P c , where P c is referred to on an absolute pressure scale, for temperatures at least about 0.9 T c .
- solid alkylation catalyst reactivation can be achieved by contacting the at least partially deactivated catalyst with a fluid reactivation agent at certain temperatures and pressures. These pressures and temperatures are such that the fluid reactivating agent is maintained fluid and dense enough so that the catalyst fouling agents and products of any reaction of fouling agents with the fluid reactivating agent can be dissolved in the fluid reactivating agent.
- the pressure should be such that the fluid reactivating agent is a dense fluid, such as a dense supercritical fluid, a dense critical fluid, a near-critical liquid, or a dense near-critical gas.
- the temperature should be such that the fluid reactivating agent's density has not decreased so much that the fluid reactivating agent can no longer effectively dissolve the catalyst fouling agents and products of any reaction of fouling agents with the fluid reactivating agent.
- T c and critical pressure P c of the fluid reactivating agent this is achieved within a temperature range that encompasses near-critical and critical temperatures, sucft as temperatures of at least about 0.9 T c and within a pressure range that encompasses near-critical and critical pressures, such as pressures that are at least about 0.1 P c .
- the pressure should be sufficiently high within practical limits so that the fluid is dense enough to have the desired solvent properties at a given temperature.
- the fluid reactivating agent is preferably at a pressure in the range of about 0.1 P c to about 10 P c more preferably about 0.9 P c to about 10 P c , andmost preferably about 1 P c to about 6 P c ; and at a temperature preferably in the range of about 0.9 T c to about 1.3 T c , and more preferably about 0.95 T c to about 1.2 T c .
- a pressure sufficient to maintain the fluid reactivating agent in a liquid phase is, utilized, with a temperature of at least about 0.9 T c , and preferably a temperature in the range of about 0.9 T c to about 1 T c .
- the fluid reactivating agent is preferably at a pressure in the range of about 0.1 P c to about 1 P c .
- the fluid reactivating agent is at a pressure equal to P c and at a temperature equal to T c .
- the fluid reactivating agent When the pressure and temperature conditions are such that the fluid reactivating agent is a supercritical fluid, the fluid reactivating agent is at a pressure greater than P c and at a temperature greater than T c . At supercritical conditions, the fluid reactivating agent is preferably at a pressure in the range of about 1 P c to about 8 P c , and at a temperature preferably in the range of about 1 T c to about 1.3 T c .
- Wavy lines 8 and 9 in Figure 2 indicate that the pressure and temperature conditions for the reactivating process according to the present invention do not necessarily have to be confined to the supercritical fluid region ofthe phase diagram.
- the pressure and temperature conditions extend, as noted above, outside the supercritical fluid region for the reactivating agent.
- a reactivating agent in the context of this invention is understood to be a compound capable of dissolving some or all of the fouling agents in a catalyst.
- the reactivating agent also reacts with some or all ofthe fouling agents.
- a preferred fluid reactivating agent in the context of this invention is a branched paraffin containing at least one tertiary carbon (a carbon atom single-bonded to three other carbon atoms).
- isobutane has effectively been used in the context of this invention as a good fluid reactivating agent.
- Another fluid reactivating agent in the context of this invention is isopentane.
- Still another embodiment ofthe fluid reactivating agent within the scope of this invention is a mixture of isobutane and isopentane.
- Yet another embodiment is the use as fluid reactivating agent of additional compounds that contain at least one tertiary carbon, such as 2,3- dimethylbutane; 2- and 3-methylpentanes; 2,3- and 2,4-dimethypentanes; 2- and 3- methylhexanes; 2,3-, 2,4-, 2,5-, and 3,4-dimethylhexanes; 2,3,4-trimethylhexane; and the like.
- these compounds may contain more than one tertiary carbon atom.
- Compounds such as straight-chain hydrocarbons that can be isomerized over the catalyst to compounds containing tertiary carbon atoms are also included as embodiments ofthe present invention.
- isomerizable compounds examples include n-butane which isomerizes to a small degree to isobutane, and n-pentane which can isomerize to isopentane.
- Other useful compounds include reactive or isomerizable/non- reactive fluid reactivating agent compounds that do not contain tertiary carbons, but are capable of hydride transfer reactions, such as toluene, benzene, ethylbenzene, or other aromatic compounds.
- Further useful compounds for the fluid reactivating agent include fluid solvent compounds which can react with fouling agents in manners different than hydride transfer.
- branched paraffin refer herein to at least one branched paraffin.
- these terms encompass embodiments such as one single branched paraffin, a mixture of branched paraffins, and mixtures containing at least one branched paraffin which perform as the fluid reactivating agent of this invention that is embodied by at least one branched paraffin.
- Other embodiments of the fluid reactivating agent of this invention include mixtures of isoparaffins and hydrocarbons.
- Still other embodiments of the fluid reactivating agent of this invention include mixtures of a hydrocarbon with at least one gas such as hydrogen and oxygen.
- Examples of these embodiments include a mixture of isobutane and hydrogen, a mixture of isopentane and hydrogen, a mixture of isobutane, isopentane and hydrogen, and mixtures of any ofthe above example compounds or similar compounds with hydrogen.
- the choice of the specific fluid reactivating agent depends in part on the pressure and temperature conditions at which the catalyst reactivation is to be performed. Known correlations between the number of carbon atoms of isoparaffins, easily derivable from tables of critical constants, can be readily employed to choose a specific hydrocarbon or hydrocarbon mixture as the fluid reactivating agent.
- the critical pressure decreases as the number of carbon atoms increases in the series including isobutane, isopentane, and 2,3-dimethylbutane or 2-methylpentane.
- the critical temperature increases as the number of carbon atoms for the same compounds increases.
- the temperature and pressure conditions ofthe fluid reactivating agent such as isobutane employed in a method for reactivating a solid alkylation catalyst according to the invention are such that the temperature is preferably in the range of about 94°C to about 250°C, and more preferably about 150°C to about 210°C, and the pressure is preferably in the range of about 200 psig to about 5000 psig.
- the catalyst to be reactivated by the methods of this invention can be any of the catalysts that are known to be effective in alkylation reactions.
- the fluid reactivating agent is such that it can penetrate into the channels or other voids or regions where the catalyst's deactivated sites are located. This is determined by the size and shape ofthe channels, voids or; other spaces defined by the structure ofthe catalyst. As discussed above, the size and dimensions of species that are to effectively interact with the fouling agents that occupy the active sites of catalysts of varying structures are known, and thus the appropriate fluid reactivating agent can be chosen for each alkylation catalyst.
- the present invention further proyides the benefit of reducing or eliminating the need for oxidative regeneration of catalysts, thereby maintaining catalyst activity for longer periods of time which reduces the frequency of catalyst replacement and the accompanying cost.
- Example 1 The experiments performed with flows and reaction conditions within the ranges given in this set of examples were performed with a two-column swing system such as the system schematically shown in Figures 1A and IB.
- Reactor 1 was fed with a mixture of isobutane and trans-2-butene in a molar ratio that ranged from 1:1 to 100:1 referring to the isobutane:olefm molar ratio.
- Alkylation temperatures ranged from about 5°C to about 90°C, and pressures ranging from ambient pressure to about 2100 psig.
- Isobutane or other reactivating agents were fed to reactor 2 to reactivate the alkylation catalyst contained therein. Temperature in reactor 2 ranged from about 130°C to about 250°C, and the pressure in, the same reactor ranged from about 500 psig to about 4000 psig. Pressure and temperature were combined so that the isobutane or other reactivating agents were maintained in some trials in supercritical conditions whereas, in some other trials, slightly outside the supercritical region.
- the OWHSV was 0.2 g olefin (g catalyst) "1 h "1 and the IWHSV was 4.14 g isobutane (g catalyst) "1 h” 1 in the same reactor.
- the RWHSV in reactor 2 ranged from about 24 to about 48 g reactivating agent (g catalyst) "1 h "1 .
- the alkylation catalyst in reactor 2 was reactivated in about 2 h at reactivation conditions.
- Example 2 Experiments were conducted in a plug-flow reactor system using 1 gram of catalyst packed into a stainless steel tubular reactor.
- the catalyst utilized for the experiments was a USY Zeolite catalyst.
- the isoparaffin to olefin ratio was 20: 1 on a molar basis, while the olefin weight-h ⁇ r-space velocity (OWHSV) was set at 0.2 g trans-2-butene (g catalyst) "1 h '1 .
- Reaction conditions were 60°C and 1600 psig, set so that the reaction occurred in the liquid phase.
- the reactivation was done using 99.5% isobutane (or other control reactivating agents), at various throughputs.
- the reactivation temperatures were varied from 130 to 210°C and the pressures from 1000 to 3180 psig.
- Reactivation time (at conditions) was varied from 0.5 to 3 hours.
- the run and reactivation procedures were as follows: The system was started initially with isobutane, at 60°C and 1600 psig, throughout. At time zero, flow of reaction mixture (isobutane and trans-2-butene, as described above) was started.
- reaction mixture flow was stopped, and the desired flow rate of fluid reactivating agent (control reactivating agents or isobutane), at
- Reactivation conditions were held at the desired values for the desired period of time, after which the conditions were adjusted back to 60°C and 1600 psig over 20-
- Yields of product from the reaction were calculated by integrating the production rate versus time data.
- the production rate (g product (g catalyst)" 1 h” 1 ) data were calculated from the feed input rate (g feed (g catalyst)" 1 h "1 ) and the product weight fraction (wt%) and plotted versus time.
- An example plot ofthe data for total alkylate (C5+) and for trimethylpentanes (TMP) is shown in Figure 3.
- the initial reaction and reactivated catalyst reaction peaks were integrated, and the percentage of activity recovered was calculated by dividing the second peak area by the first peak area and multiplying by 100%.
- Reactivation conditions for the example shown were 150°C, 1600 psig, 33 g isobutane fed (g catalyst)" 1 h" 1 , for two hours (at reactivation conditions).
- TMP Trimethylpentanes
- Reactivating agents that are in the supercritical phase test the additional effect of supercritical fluid extraction (SFE) on reactivation. Adjusting reactivation conditions to give a constant density reactivating agent (set to the density of isobutane at 180°C, 1600 psig) tests the effectiveness of each supercritical fluid at the same density (p) on recovery of activity. Finally, the use of reactivating agents that contain at least one tertiary carbon atom tests the effect on activity recovery of using a reactive reactivating agent (R).
- the reaction phase in each experiment in summarized Table 3 was run as in the examples above, at 60°C, 1600 psig, a molar isobutane:trans-2-butene ratio of 20: 1 , and an OWHSV of 0.2.
- n-butane 140 1600 NC liq. / / 30 n-butane 180 1600 SCF / / / 51 n-butane 180 1310 SCF / / / 46 n-pentane 180 1600 NC liq. / / 22 n-pentane 210 1600 SCF / / / 40 n-pentane 210 915 SCF / / / / 42
- Reactive Reactivating Agents isobutane 60 1600 Liquid / / 0.4 isobutane 90 1600 Liquid s* / / 3
- the reactivating agents n-pentane and n-butane isomerize to a small degree ( ⁇ 1%) over acid catalysts to form isopentane and isobutane, respectively, which contain a tertiary carbon atom and can therefore take place in the hydride transfer reaction during reactivation.
- a small but undetermined amount of the recovered activity may be due to reactivity of the isomerized reactivating agent.
- the data provided hereinabove show that simple thermal cracking and volatilization using helium can recover about 33% ofthe initial activity.
- the data also show that a liquid phase reactive reactivating agent cannot reactivate the catalyst to a significant degree once it has been completely deactivated.
- the amount of activity recoverable decreases with decreasing reactivation temperature (i.e., activity recovery using isobutane: 180°C > 130° C> 90°C > 60 °C; see also Figure 6), indicating that thermal cracking plays an important role in the reactivation of completely deactivated catalyst.
- decreasing to a liquid phase from near- critical liquid conditions by lowering the temperature eliminates the regenerative nature ofthe reactivation procedure.
- a non-reactive reactivating agent that cannot isomerize to a reactive reactivating agent recovers less activity than a non-reactive reactivating agent that can isomerize to a reactive reactivating agent (i.e., SCFs: propane (24%) ⁇ n-butane (51%) or n-pentane (40%); Constant density SCFs: propane (28%) ⁇ n-butane (46%) or n-pentane (42%)).
- SCFs propane (24%) ⁇ n-butane (51%) or n-pentane (40%)
- Constant density SCFs propane (28%) ⁇ n-butane (46%) or n-pentane (42%)
- NC liquid, SCF non-reactive reactivating agents
- reactivation using non-reactive reactivating agents generally decreases with increasing molecular weight (i.e., NC liquids: n-butane (30%o) > n-pentane (22%); SCFs: n-butane (51%) > n-pentane (40%); Constant density SCFs: n-butane (46%) > n-pentane (42%)).
- reactivations run in the SCF phase when conditions were maintained at the same pressure and at similar temperatures as in the NC liquid phase, were generally more effective than those run in the NC liquid phase with the same reactivating agent, whether the reactivating agent was reactive or non-reactive (i.e., Changing fromNC liquid to SCF results in: n-butane (30% to 51%); n-pentane (22% to 40%); isobutane (50% to 82%); isopentane (59% to 65%)).
- the data show that supercritical phase is preferred over Liquid phase and NC liquid conditions.
- the data also show that thermal cracking is an important part ofthe regenerative nature ofthe reactivation procedure.
- reactive reactivating agents are generally preferred over non-reactive reactivating agents, although even isomerizable non-reactive reactivating agents such as n-butane and n-pentane in the supercritical phase can be useful in the methods of the invention.
- isobutane (reactive) is generally preferable over n-butane (non- reactive)
- isopentane (reactive) is generally preferable over n-pentane (non- reactive).
- n-butane is preferred over n-pentane when they are maintained at similar thermodynamic conditions.
- isobutane is generally preferable over isopentane.
- the compound that can isomerize to a reactive compound is preferred over the one that cannot isomerize.
- n- butane and n-pentane are generally preferred over propane.
- a preferred feature ofthe reactive fluid reactivating agent is a tertiary carbon atom, which is believed to allow the fluid reactivating agent molecule to participate in hydride transfer during reactivation.
- the recovery enhancement was seen in both NC liquid (isopentane versus n-pentane) and SCF (isobutane versus n-butane and propane) phases, but not in the liquid phase.
- Example 3 A series of experiments were performed to determine the effect of reactivation conditions on activity recoyery with isobutane for a completely deactivated catalyst under near-critical to supercritical conditions, since it was shown that there is no significant reactivation of completely deactivated catalyst in the liquid phase. Variables included reactivation temperature, pressure, time, and isobutane throughput. In addition, experiments using the temperature, time, and isobutane throughput values and varied pressure to obtain a constant isobutane density were performed. Reaction conditions were as in Example Set 2, at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h "1 .
- Reactivation protocols were also as described in Example Set 2, but using isobutane always as the fluid reactivating agent. It was found that about 33 g isobutane (g catalyst) "1 h "1 is a preferred isobutane throughput with a reactivation time (at reactivation temperature and pressure) of 2 hours. Temperatures from 130-210°C (0.99-1.19 T c ) were tested, ranging from near-critical liquid to supercritical. Pressures were varied from 1000- 3180 psig (1.86- 5.87 P c ). The results for temperature, pressure, and temperature at constant density are presented in Figures 6, 7, and 8, respectively.
- the molar isoparaffin to olefin ratio was 20:1, while the OWHSV ranged from 0.2-0.4 g trans-2-butene (g catalyst) "1 h “1 .
- Reaction conditions were again 60°C and 1600 psig.
- the reactivation was done as above, at 33 g isobutane (g catalyst) "1 h “1 , for 2 hours (at conditions).
- the reactivation temperature and pressure were 180°C and- 1600 psig, respectively.
- the run and reactivation procedures were as before, with the following modifications.
- the system was started with the recycle pump "ON.” The reaction was allowed to proceed until a desired level of activity (that served as a criterion for starting the reactivation) was reached.
- reaction mixture flow was stopped, and flow of 33 g isobutane (g catalyst) "1 h "1 , at 60°C and 1600 psig,. was started.
- the recycle pump was left “ON” to clear the recycle line of products and trans-2-butene. These conditions were maintained for 10 minutes or long enough to sweep the reactants from the catalyst bed.
- the recycle pump was then shut off and the temperature was adjusted to 180°C over 20-30 minutes. Reactivation conditions were held at 180°C and 1600 psig for 2 h, after which the conditions were adjusted back to 60°C and 1600 psig over 20-30 minutes. Once back at the reaction conditions, the recycle pump was turned “ON.” After 5 minutes, the reaction mixture flow was restarted and the reaction was allowed to proceed until the desired criterion was again reached. Yields of product from the reaction were calculated as above.
- Table 4 summarizes the results of plug flow experiments with recycle reactivation run at 0.2 and 0.4 WHSV, using as reactivation criteria both a specified butene conversion (before and after reactivation) and identical times for each run (before and after reactivation).
- Reaction was done at 60°C, 1600 psig, OWHSVs of 0.2 or 0.4 g trans-2-butene (g catalyst): 1 h " ,!, .and an isoparaffin: olefin ratio of 20: 1. Note for the rightmost columns that the butene conversion reached the stop criterion for the second run (after reactivation) in a shorter period of time than in the first run, and therefore recovery values were less than 100% of the initial activity.
- the recoveries were generally greater than 100% ofthe initial activity. This is because the reactive reactivation method activates the catalyst active sites, thus reducing the catalyst induction period and increasing the initial rate of product formation. This results in higher yields after reactivation versus fresh catalyst, in equal time periods.
- Example 5 Recycle plug flow experiments utilizing multiple reactivation runs (more than one reactivation) were conducted to determine a preferred upper bound for the number of reactivations possible under the conditions at which these experiments were conducted. The experiments were done using reaction conditions as reported in Example Set 4, ranging in OWHSV from 0.2-0.4 g trans-2-butene (g catalyst)" 1 h" 1 . Reactivation was with isobutane as above; the reactivation criteria were that butene conversion dropped to 95% or 90% for 0.2 and 0.4 OWHSV, respectively.
- Figures 9-14 show the C5+ and TMP production results and run times for a complete multiple reactivation experiment at an OWHSV of 0.2.
- Figure 9 shows the C5+ and TMP yields (per unit butene fed to the alkylation reactor) versus total experimental run time.
- Figures 10-12 show the variations in reaction run time, % recovered catalyst activity, and product yields (per gram of catalyst) with each successive reactivation. Cumulative product yields and catalyst life are shown in Figures 13 and 14.
- product yields and run times decreased slowly over time because the net OWHSV in the reactor slowly increased due to increasing deactivation with each successive run.
- activity leveled off after a time approaching a steady state between deactivation and reactivation.
- Activity could be maintained at reduced levels over at least 8 reactivations without requiring oxidation at an OWHSV of 0.2, using 95% butene conversion as the reactivation criterion.
- the reactivation procedure provided a net catalyst life of about 42 h through eight reactivations.
- Example 6 Recycle plug flow experiments utilizing multiple reactivation runs (more than one reactivation) were conducted as described in Example Set 5 above, at an OWHSV of 0.2 g trans-2-butene (g catalyst) "1 h "1 . Reactivation was again with isobutane as above; the reactivation criteria were that the alkylation had proceeded to exactly 3 h of alkylation.
- Figures 15-20 show the C5+ and TMP production results and run times for a complete multiple reactivation experiment at an OWHSV of 0.2.
- Figure 15 shows the C5+ and TMP yields (per unit butene fed to the alkylation reactor) versus total experimental run time.
- Figures 16-18 show the variations in reaction run time, % recovered catalyst activity, and product yields (per gram of catalyst) with each successive reactivation. Cumulative product yields and catalyst life are shown in Figures 19 and 20.
- Example 7 Overall yields were less per alkylation run than those observed in Example Set 5 because the alkylation run time was lower (and thus the catalyst deactivation proceeded further before reactivation with isobutane). However, the net effect of reactivation at lower levels of catalyst deactivation was to increase the overall catalyst lifetime to sustainable or near-sustainable catalyst activity. This allowed higher overall amounts of product formation from the same batch of catalyst. In Figure 16, the alkylation run times are shown to indicate a constant alkylation time of 3 hours. Example 7
- the catalyst is removed from the reactor by gravity or forced flow, separated from the reaction mixture, mixed with a stream of fluid reactivating agent, and passed through a region with the temperature and pressure set for reactivation as described in the foregoing examples. This procedure permits the continuous reactivation ofthe alkylation catalyst before its complete deactivation.
- Catalyst movement is not restricted to a CSTR.
- the regeneration process is adaptable to any type moving bed reagtor system.
- a variety of reactor configurations can be utilized to transport catalyst from the alkylation reactor zone to the regeneration zone.
- the continuous reactivation process ofthe present invention can be adapted to maintain high catalytic activity.
Abstract
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US8395006B2 (en) | 2009-03-13 | 2013-03-12 | Exxonmobil Research And Engineering Company | Process for making high octane gasoline with reduced benzene content by benzene alkylation at high benzene conversion |
Also Published As
Publication number | Publication date |
---|---|
US6887813B2 (en) | 2005-05-03 |
AU2001268423A1 (en) | 2001-12-24 |
US20080267835A1 (en) | 2008-10-30 |
EP1301270A4 (en) | 2004-10-13 |
EP1301270A1 (en) | 2003-04-16 |
US6579821B1 (en) | 2003-06-17 |
CA2411091A1 (en) | 2001-12-20 |
US7670568B2 (en) | 2010-03-02 |
US20030207751A1 (en) | 2003-11-06 |
CA2411091C (en) | 2005-06-14 |
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