US2583013A - Condensation of sublimable material - Google Patents
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- US2583013A US2583013A US624767A US62476745A US2583013A US 2583013 A US2583013 A US 2583013A US 624767 A US624767 A US 624767A US 62476745 A US62476745 A US 62476745A US 2583013 A US2583013 A US 2583013A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D7/00—Sublimation
- B01D7/02—Crystallisation directly from the vapour phase
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/54—Preparation of carboxylic acid anhydrides
- C07C51/573—Separation; Purification; Stabilisation; Use of additives
Definitions
- the present invention is directed to a method for recovering from a vaporous product stream, a product which is normally solid and is capable of undergoing sublimation.
- a typical product of this type is phthalic anhydride, produced by the oxidation of naphthalene or ortho-xylene.
- a sublimable constituent is removed from a vaporous mixture by passing the mixture through a cooling zone in which is maintained a suspension of the sublimable material in solid form and in a state of turbulent motion; preferably the vaporous mixture is passed upwardly through the cooling zone-at 'a velocity sufficient to maintain the finely divided solid sublimable constituent in. the desired state of suspension.
- the velocity of flow of the vaporous mixture issuch as to carry the finely divided solid suspended init through the cooling zone at a lesser rate than the vaporous mixture itself. In this type of operation all of the solid material is carried out of the top of the cooling zone.
- the velocity of the vaporous mixture is such as to carry the solid sublimable material only partly through the cooling zone where itis concentrated in what may be termed a dense phase from which the solid material drops out by gravity and is withdrawn from the bottom of the zone while the residual vapors pass out overhead.
- the presence of the solid sublimable material in the cooling zones erves several purposes; first, it provides nuclei for the deposition of sublimable material from the vaporous state. Second, it serves to scour the cooling surfaces, keeping them clear of incrustations. Third, it improves the heat transfer between the cooling surfaces and the vapors.
- the solid sublimable material is p recooled. In its precooled state ithas the ability of taking up considerable quantities of heat from the vaporous mixture. It therefore contributes directly to the condensation of the sublimable constituent in the vaporous mixture.
- FIG. 1 is a front elevation partly in section, of one type of apparatus suitable for the practice of the present invention
- Figure 2 is a similar view of a modified form of apparatus
- Figure 3 is a similar view of a condensation chamber of the type shown in Figure 1;
- Figure 4 is a transverse section alongthe line AA of Figure 3.
- numeral I designates a vessel or shell enclosing the condensation zone. Inside this vessel is mounted a bundle of tubes 2 having their ends mounted in webs 3 having inclined surfaces. The webs 3 are welded or otherwise connected to the vessel I so as to form a fluid-tight zone around the tubes 2. An inlet 4 for cooling fluid into the zone is provided near the bottom thereof, while an oulet 5 for this fluid is provided near the top of said zone. At the bottom of the vessel is a line 6 for the introduction of a vaporous mixture containing a sublimable material. At the upper end of the vessel is an outlet I for vaporous residue carr ng the sublimable material in solid form.
- This line discharges into a separator 8 in the upper portion of which is mounted a cyclone separator 9.
- the residual vapors leave the settler '8 through the line H) while separated solids fall to theibottom of the settler, some entering the settler through the doWnp-ipe H of the cyclone sep-, arator.
- the lower portion of the settler is divided into two hoppers l2 and I3, between which there is a partition M which may be swung into any desired position to regulate the amount of solid material which falls into the respective hoppers.
- Hopper I3 discharges into a cooling zone l5 provided with a cooling coil I6. If desired, the vaporous outlet from line II) can be fed through this cooling coil.
- The-lower end of the hopper I2 is provided with a slide valve or other suitable valve I! for the withdrawal of solid product from the system.
- the solid sublimable material passes through the cooling zone l5 and collects at the bottom thereof, from which it is fed by means of a star Wheel [8 or other suitable feeding device into inlet line 6.
- a star Wheel [8 or other suitable feeding device into inlet line 6.
- suitable verticaland circumferentiallyspaced nozzles IS on this chamber through which may be injected a fluidizing gas.
- This expedient serves to maintain the solid in the cooling zone in 3 a fluidized condition in which it acts as a liquid having a head which exerts a propelling force in the system.
- the residual vapors leaving through line 10, or part thereof may be supplied to the injection nozzles l9 to serve as the fluidizing medium in zone l5.
- star wheel or similar feeding mechanism may be dispensed with andsufiicient' head of fluidized solid maintained in the cooling zone is to cause the fluidized solid to feed into inlet line 6 at any desired rate adjusted with respect to the feed rate of the vapors in line 6 to maintain the desired density of solids in the condenser I.
- the vaporous product is preliminarily cooled by passage through cooling coils to a temperature of about 300 C. so that when the solid phthalic anhydride is introduced into the mixture it will not readily sublime.
- thecooling coil 56 may be dispensed with or may be used to circulate cold .water if desired. It is sufficient, however, that the solid phthalic anhydride be at about room temperature or even somewhathigher.
- the vaporous mixture containing the solid phthalic anhydride is fed into the bottom of the vessel i through the tube bundle 2 around which may be circulated water.
- the veolcity of the vapors is so maintained that it carries the. solid. phthalio anhydride through the vessel l at a lower rate than it travels itself, whereby the solid phthalie anhydride has a longer residence time in the tube. bundle than. the vaporous material.
- the amount of solid added to the condenser should be sufiicient with relation to the velocity of the vapors through the condenser to maintain at least about 5# per cubic foot of vapor space. This requires a fairly low velocity of vapors through the condenser, as for example, from 3 to 7 feet per second. With a velocity in this range, the solids are added to vapor stream or the condenser at a rate of from about 10 to 100# per minute per square foot of cross-section of vapor spaced oi condenser.
- FIG. 2 there is illustrated what may be referredto asthe downflow type of operation.
- the vessel It is provided with a cooling coil 28 and at its upper end with a cyclone separator 2
- the downpipe discharges into the open mouth of a funnel 24 arranged below the cooling coil, the spout of which is con neeted to a pipe 25 which enters through the lower end of the vessel and through which the vaporous mixture containing the sublimable mixture is introduced.
- a hopper .30 in which is arranged a worm .31
- the vaporous mixture carrying the solid sublimable material is fed into the vessel at a velocity such that the solid material is carried only about the top of the cooling coil, forming around the coila condition which may be referred. to as a densephase.
- a densephase which may be referred. to as a densephase.
- the effect is that of a fountain, with the solid material coming up the middle and descending along the outside. The bulk of the solid material will not get beyond the dense phase.
- Such lesser amounts as are carried upwardly into the cyclone separator are separated from the vaporousresidue and returned to the dense phase.
- the solid is added to the condenser at a rate so adjusted to the vapor flow as to maintain in the condenser at least about 10? per cu. ft. of vapor space.
- This requires a relatively low vapor velocity, as for example, from about .5 to about 5 feet per second through the condenser. With such velocities the solid is added to the condenser at a rate between about 104% and 500# per minute per square foot of cross-section of vapor space of condenser.
- In Figure3 is shown a type of .tube bundle that is particularly usul for the practice of 'the present invention.
- the shell is indicated by numeral I and the individual tubesby numeral 2;, while the web by which the tube bundle is connected to the shell is indicatedby numeral 3.
- each tube has both ends flared outwardly,,as at 4, with theouter edge having a a polygonal configuration 5, in this case, hexagonal.
- this construction eliminates all transverse surfaces at the ends of the tube bundle, presenting only sharp edges to, the material en-. tering the bundle.
- the entrance to theindividual tubes is streamlined so that a mini-v mum of resistance is offered to any fluid passing through the bundle.
- a method for recovering from a vapor stream a contained product which is, normally solid, and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable toeffectasolidification ofthe product in the presenceof .added solid particles of the product, separating the solid product from residual vapors and feeding back some of said solid product to the vapor stream entering the cooling zone, while maintaining a sufiicient velocity in said vapor stream to carry said recycled solid product along with such stream in a state of turbulent motion.
- a method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added particles of the solidified product, removing the residual vapor stream and solidified product from the cooling zone, separating the solidified product from the vapor stream and returning a portion of said solidified product to the cooling zone together with a fresh quantity of vapor stream.
- a method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added solid particles, simultaneously introducing into said cooling zone a finely divided solid, adjusting the rate of fiow of said vapors and the rate of introduction of said solid so as to maintain in said cooling zone a density of said solid at least about 5# per cubic foot of vapor space, continuously removing vapor stream carrying entrained solid from said cooling zone and separating said solid from said vapor stream.
- a method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added solid particles, simultaneously introducing into said cooling zone a finely divided solid, adjusting the velocity of said vapor stream to said cooling zone to a value between about .5 and 5 feet per second and simultaneously adjusting the rate of feed of finely divided solid of at least per cubic foot of vapor space, removing vapor stream carrying entrained solid from said cooling zone, and separating the solid from the vapor stream.
- a method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing said vapor stream through a line and 6 thence into a cooling zone, establishing in a vertical column, in direct communication with said line, a head of fluidized finely divided solid whereby said fluidized solid is continuously fed into said vapor line and thence into the cooling zone wherein the sublimable material is solidified on said fluidized solid, recovering from said cooling zone a vapor stream carrying entrained solid and separating said solid from said stream.
- a method for recovering solidified phthalic anhydride from a vapor stream formed by catalytic oxidation of an aromatic hydrocarbon which comprises passing said vapor stream through a cooling zone, adding cooler preformed phthalic anhydride particles to said vapor. stream being passed into said cooling zone, cooling the vapor stream containing phthalic anhydride vapor by heat transfer to the added solid particles and to cooling surfaces in said cooling zone without diluting the vapor by extraneous gas, solidifying phthalic anhydride from its vapor in said stream on to said added solid particles, concentrating and separating the resulting solid particle product into a dense fluidized phase from the remaining vapor stream leaving the cooling zone, and withdrawing a product stream of the resulting solid particles from said dense phase.
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Description
Jan. 22, 1952 J. A. PATTERSON 2,533,013
CONDENSATION 0F SUBLIMABLE MATERIAL Filed Oct. 26, 1945 3 Sheets-Sheet 2 VE$$L FIG-2 Jam. 22, 1952 l J. A. PATTERSON 2,583,0
CONDENSATION OF SUBLIMABLE MATERIAL Filed Oct. 26, 1945 I s Sheets-Sheet 3 Patented Jan. 22, 1 952 2,583,013 CONDENSATION OF SUBLIMABLE MATE RIAL
John A. Patterson, Westfield, N. J., assignor to Standard Oil Development Company, a. corporation of Delaware Application October 26, 1945, Serial No. 624,767
Claims. I l
- The present invention is directed to a method for recovering from a vaporous product stream, a product which is normally solid and is capable of undergoing sublimation. A typical product of this type is phthalic anhydride, produced by the oxidation of naphthalene or ortho-xylene.
According to the present invention, a sublimable constituent is removed from a vaporous mixture by passing the mixture through a cooling zone in which is maintained a suspension of the sublimable material in solid form and in a state of turbulent motion; preferably the vaporous mixture is passed upwardly through the cooling zone-at 'a velocity sufficient to maintain the finely divided solid sublimable constituent in. the desired state of suspension. In one type of operation the velocity of flow of the vaporous mixture issuch as to carry the finely divided solid suspended init through the cooling zone at a lesser rate than the vaporous mixture itself. In this type of operation all of the solid material is carried out of the top of the cooling zone. In another type of operation the velocity of the vaporous mixture is such as to carry the solid sublimable material only partly through the cooling zone where itis concentrated in what may be termed a dense phase from which the solid material drops out by gravity and is withdrawn from the bottom of the zone while the residual vapors pass out overhead.
The presence of the solid sublimable material in the cooling zoneserves several purposes; first, it provides nuclei for the deposition of sublimable material from the vaporous state. Second, it serves to scour the cooling surfaces, keeping them clear of incrustations. Third, it improves the heat transfer between the cooling surfaces and the vapors. In this connection in the preferred mode of operation, according to the present invention, the solid sublimable material is p recooled. In its precooled state ithas the ability of taking up considerable quantities of heat from the vaporous mixture. It therefore contributes directly to the condensation of the sublimable constituent in the vaporous mixture.
- In the condensation of a sublimable substance from a vapor mixture, there is frequently formed a fog due to overcooling of the vapor. This fog contains the solid in a form which separates from the vapor with considerable diificulty. The formation of such fogs is inhibited or repressed bythe presence of the suspended particles in a state of turbulent flow in accordance with the present invention.
The nature and objects of the present inven- 2 tion may be more clearly understood from the following detailed description of the accompanying drawing, in which:
- Figure 1 is a front elevation partly in section, of one type of apparatus suitable for the practice of the present invention;
Figure 2 is a similar view of a modified form of apparatus;
Figure 3 is a similar view of a condensation chamber of the type shown in Figure 1; and
Figure 4 is a transverse section alongthe line AA of Figure 3.
Referring to the drawing in detail, numeral I designates a vessel or shell enclosing the condensation zone. Inside this vessel is mounted a bundle of tubes 2 having their ends mounted in webs 3 having inclined surfaces. The webs 3 are welded or otherwise connected to the vessel I so as to form a fluid-tight zone around the tubes 2. An inlet 4 for cooling fluid into the zone is provided near the bottom thereof, while an oulet 5 for this fluid is provided near the top of said zone. At the bottom of the vessel is a line 6 for the introduction of a vaporous mixture containing a sublimable material. At the upper end of the vessel is an outlet I for vaporous residue carr ng the sublimable material in solid form. This line discharges into a separator 8 in the upper portion of which is mounted a cyclone separator 9. The residual vapors leave the settler '8 through the line H) while separated solids fall to theibottom of the settler, some entering the settler through the doWnp-ipe H of the cyclone sep-, arator. The lower portion of the settler is divided into two hoppers l2 and I3, between which there is a partition M which may be swung into any desired position to regulate the amount of solid material which falls into the respective hoppers. Hopper I3 discharges into a cooling zone l5 provided with a cooling coil I6. If desired, the vaporous outlet from line II) can be fed through this cooling coil. The-lower end of the hopper I2 is provided with a slide valve or other suitable valve I! for the withdrawal of solid product from the system.
The solid sublimable material passes through the cooling zone l5 and collects at the bottom thereof, from which it is fed by means of a star Wheel [8 or other suitable feeding device into inlet line 6. In order to avoid packing of the solids in the cooling zone I5, it is preferred to provide suitable verticaland circumferentiallyspaced nozzles IS on this chamber through which may be injected a fluidizing gas. This expedient serves to maintain the solid in the cooling zone in 3 a fluidized condition in which it acts as a liquid having a head which exerts a propelling force in the system. For this purpose the residual vapors leaving through line 10, or part thereof, may be supplied to the injection nozzles l9 to serve as the fluidizing medium in zone l5. Also the star wheel or similar feeding mechanismmay be dispensed with andsufiicient' head of fluidized solid maintained in the cooling zone is to cause the fluidized solid to feed into inlet line 6 at any desired rate adjusted with respect to the feed rate of the vapors in line 6 to maintain the desired density of solids in the condenser I.
In the case of the recovery of. phthalic anhy-' dride, for example, from a vaporous reaction mixture containing it, as for example, the reaction mixture resulting from the vapor phase oxidation of naphthalene, the vaporous product is preliminarily cooled by passage through cooling coils to a temperature of about 300 C. so that when the solid phthalic anhydride is introduced into the mixture it will not readily sublime. In this operation thecooling coil 56 may be dispensed with or may be used to circulate cold .water if desired. It is sufficient, however, that the solid phthalic anhydride be at about room temperature or even somewhathigher. The vaporous mixture containing the solid phthalic anhydrideis fed into the bottom of the vessel i through the tube bundle 2 around which may be circulated water. The veolcity of the vapors is so maintained that it carries the. solid. phthalio anhydride through the vessel l at a lower rate than it travels itself, whereby the solid phthalie anhydride has a longer residence time in the tube. bundle than. the vaporous material. The mixturedischarges into settler. 8 where the solid phthalic anhydride falls to .the bottom, part going into discharge hopper l2 and the remainder going into the return hopper l3. It will be understood that instead of feeding the solid phthalic anhydride to the line B it may be blown directly into the bottom of vessel 1 near the inlet to the tube bundle to eliminate the possibility of any sublimation of the recycled phthalic anhydride.
When the system is in operation, the amount of solid added to the condenser should be sufiicient with relation to the velocity of the vapors through the condenser to maintain at least about 5# per cubic foot of vapor space. This requires a fairly low velocity of vapors through the condenser, as for example, from 3 to 7 feet per second. With a velocity in this range, the solids are added to vapor stream or the condenser at a rate of from about 10 to 100# per minute per square foot of cross-section of vapor spaced oi condenser.
.In Figure 2 there is illustrated what may be referredto asthe downflow type of operation. In this operation the vessel It is provided with a cooling coil 28 and at its upper end with a cyclone separator 2| having a vapor exhaust line 22 anda downpipe 23. The downpipe discharges into the open mouth of a funnel 24 arranged below the cooling coil, the spout of which is con neeted to a pipe 25 which enters through the lower end of the vessel and through which the vaporous mixture containing the sublimable mixture is introduced. At its lowermost portion the I of a hopper .30 in which is arranged a worm .31
4 for feeding the solid material from the vessel 29 into the inlet tube 25.
In this type of operation the vaporous mixture carrying the solid sublimable material is fed into the vessel at a velocity such that the solid material is carried only about the top of the cooling coil, forming around the coila condition which may be referred. to as a densephase. Actually the effect is that of a fountain, with the solid material coming up the middle and descending along the outside. The bulk of the solid material will not get beyond the dense phase. Such lesser amounts as are carried upwardly into the cyclone separator are separated from the vaporousresidue and returned to the dense phase.
In this-modification the solid is added to the condenser at a rate so adjusted to the vapor flow as to maintain in the condenser at least about 10? per cu. ft. of vapor space. This requires a relatively low vapor velocity, as for example, from about .5 to about 5 feet per second through the condenser. With such velocities the solid is added to the condenser at a rate between about 104% and 500# per minute per square foot of cross-section of vapor space of condenser.
InFigure3 is shown a type of .tube bundle that is particularly uselul for the practice of 'the present invention. Here again, the shell is indicated by numeral I and the individual tubesby numeral 2;, while the web by which the tube bundle is connected to the shell is indicatedby numeral 3.
As willbe seen, each tube has both ends flared outwardly,,as at 4, with theouter edge having a a polygonal configuration 5, in this case, hexagonal.
These outer edges of the tubes arev connected together by welding or brazing.
As can be seen, this construction eliminates all transverse surfaces at the ends of the tube bundle, presenting only sharp edges to, the material en-. tering the bundle. In addition, the entrance to theindividual tubes is streamlined so that a mini-v mum of resistance is offered to any fluid passing through the bundle.
In the foregoing discussion emphasis has been laced on the inclusion, in a vaporous product containing a sublimable constituent being fed. to a condensing zone, of some of the sublimable constituent in solid form. This is to be preferred where the sublimable constituent is desired as the final product. Where, however, the purpose is primarily to remove the sublimable constituent from the vaporus mixture in which it may occur as anundesirable impurity, substantially all of the advantages of the technique hereinbefore describedcan be realized by adding to the vaporous mixture any finely divided solid material which is inertto themixture. Thus finely divided clay or quartz vorvarious synthetic gels may be utilized, to. improve heat transfer and to provide nuclei for the deposition of the Sublimated material in accordance with the procedure herein described. Moreover, this technique can be utilized in the condensation of normally liquid materials from vaporous mixtures.
The nature and objects of; the present. invention having been thusv described and illustrated, what is claimed as new and useful and is desire to be secured by Letters Patent is:
l. A method for recovering from a vapor stream a contained product which is, normally solid, and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable toeffectasolidification ofthe product in the presenceof .added solid particles of the product, separating the solid product from residual vapors and feeding back some of said solid product to the vapor stream entering the cooling zone, while maintaining a sufiicient velocity in said vapor stream to carry said recycled solid product along with such stream in a state of turbulent motion.
2. A method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added particles of the solidified product, removing the residual vapor stream and solidified product from the cooling zone, separating the solidified product from the vapor stream and returning a portion of said solidified product to the cooling zone together with a fresh quantity of vapor stream.
3. A method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added solid particles, simultaneously introducing into said cooling zone a finely divided solid, adjusting the rate of fiow of said vapors and the rate of introduction of said solid so as to maintain in said cooling zone a density of said solid at least about 5# per cubic foot of vapor space, continuously removing vapor stream carrying entrained solid from said cooling zone and separating said solid from said vapor stream.
4. A method according to claim 3 in which the solid introduced into the cooling zone is the desired solid product capable of subliming.
5. A method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing the vapor stream through a cooling zone maintained at a temperature suitable to effect solidification of the product onto added solid particles, simultaneously introducing into said cooling zone a finely divided solid, adjusting the velocity of said vapor stream to said cooling zone to a value between about .5 and 5 feet per second and simultaneously adjusting the rate of feed of finely divided solid of at least per cubic foot of vapor space, removing vapor stream carrying entrained solid from said cooling zone, and separating the solid from the vapor stream.
6. A method according to claim 5 in which the finely divided solid added to the cooling zone is the desired product capable of subliming.
7. A method for recovering from a vapor stream a contained product which is normally solid and capable of subliming which comprises passing said vapor stream through a line and 6 thence into a cooling zone, establishing in a vertical column, in direct communication with said line, a head of fluidized finely divided solid whereby said fluidized solid is continuously fed into said vapor line and thence into the cooling zone wherein the sublimable material is solidified on said fluidized solid, recovering from said cooling zone a vapor stream carrying entrained solid and separating said solid from said stream.
8. A method according to claim 7 in which the solid in the head of fluidized solid is the desired sublimable product.
9. A method for recovering solidified phthalic anhydride from a vapor stream formed by catalytic oxidation of an aromatic hydrocarbon, which comprises passing said vapor stream through a cooling zone, adding cooler preformed phthalic anhydride particles to said vapor. stream being passed into said cooling zone, cooling the vapor stream containing phthalic anhydride vapor by heat transfer to the added solid particles and to cooling surfaces in said cooling zone without diluting the vapor by extraneous gas, solidifying phthalic anhydride from its vapor in said stream on to said added solid particles, concentrating and separating the resulting solid particle product into a dense fluidized phase from the remaining vapor stream leaving the cooling zone, and withdrawing a product stream of the resulting solid particles from said dense phase.
10. In the method of claim 9, the step of withdrawing a portion of the resulting solid particle product, further cooling this portion of the solid particle product, and supplying the thus cooled portion of the solid particle product as the preformed phthalic anhydride particles added to the vapor stream. JOHN A. PATTERSON.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,489,707 McKee Apr. 8, 1924 2,064,468 Foster Dec. 15, 1936 2,302,888 Porter Nov. 24, 1942 2,303,047 Hemminger Nov. 24, 1942 2,376,190 Roetheli et al. May 15, 1945 2,399,717 Arveson May 7, 1946 2,446,076 Campbell et al July 27, 1948 2,455,314 Pietzsch Nov. 30, 1948 2,475,255 Rollman July 5, 1949 FOREIGN PATENTS Number Country Date 212,671 Great Britain Mar. 20, 1944
Claims (1)
1. A METHOD FOR RECOVERING FROM A VAPOR STREAM A CONTAINED PRODUCT WHICH IS NORMALLY SOLID AND CAPABLE OF SUBLIMING WHICH COMPRISES PASSING THE VAPOR STREAM THROUGH A COOLING ZONE MAINTAINED AT A TEMPERATURE SUITABLE TO EFFECT SOLIDIFICATION OF THE PRODUCT IN THE PRESENCE OF ADDED SOLID PARTICLES OF THE PRODUCT, SEPARATING THE SOLID PRODUCT FROM RESIDUAL VAPORS AND FEEDING BACK SOME OF SAID SOLID PRODUCT TO THE VAPOR STREAM ENTERING THE COOLING ZONE, WHILE MAINTAINING A SUFFICIENT VELOCITY IN SAID VAPOR STREAM TO CARRY
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US624767A US2583013A (en) | 1945-10-26 | 1945-10-26 | Condensation of sublimable material |
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Cited By (21)
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US2702091A (en) * | 1950-05-02 | 1955-02-15 | California Research Corp | Recovery of molten phthalic anhydride |
US2721626A (en) * | 1951-12-15 | 1955-10-25 | Du Pont | Cooling and separating by condensation of hot gaseous suspensions |
US2755887A (en) * | 1956-07-24 | Melamine purification | ||
US2803311A (en) * | 1955-04-20 | 1957-08-20 | Montedison Spa | Process for separating pure, crystalline maleic anhydride directly from gaseous mixtures containing same |
US2817416A (en) * | 1954-01-28 | 1957-12-24 | California Research Corp | Liquid phthalic anhydride recovery |
US2955807A (en) * | 1954-08-02 | 1960-10-11 | United Coke And Chemicals Comp | Heat-exchange apparatus |
US3705617A (en) * | 1970-11-05 | 1972-12-12 | Badger Co | Sublimation apparatus and method |
JPS5061393A (en) * | 1973-10-02 | 1975-05-26 | ||
US3930800A (en) * | 1971-09-07 | 1976-01-06 | Aluminum Company Of America | Fluidized bed desubliming apparatus for recovery of aluminum chloride |
US3952022A (en) * | 1973-01-16 | 1976-04-20 | Rhone-Progil | Method of condensing phthalic anhydride |
FR2379481A1 (en) * | 1977-02-03 | 1978-09-01 | Aluminum Co Of America | HIGH PURITY ALUMINUM CHLORIDE PRODUCTION PROCESS |
US4478600A (en) * | 1971-09-14 | 1984-10-23 | Aluminum Company Of America | Process for recovery of aluminum chloride |
US4502871A (en) * | 1983-02-01 | 1985-03-05 | Gca Corporation | Apparatus and method for separating wax from an entrainer gas |
US4941895A (en) * | 1989-08-23 | 1990-07-17 | Amoco Corporation | Process for the continuous separation of maleic anhydride from process gases |
US5019137A (en) * | 1984-09-14 | 1991-05-28 | A. Ahlstrom Corporation | Method for cleaning gases containing condensable components |
US5032143A (en) * | 1987-05-08 | 1991-07-16 | A. Ahlstrom Corporation | Method and apparatus for treating process gases |
EP0537473A1 (en) * | 1991-10-17 | 1993-04-21 | Messer Griesheim Gmbh | Process for the recovery of solvants from waste air or gas |
FR2836059A1 (en) * | 2002-02-19 | 2003-08-22 | Ensmse | Continuous recovery process, e.g. for volatile organics, involves condensing or solidifying fraction from gaseous flow |
US20070224109A1 (en) * | 2006-03-23 | 2007-09-27 | Keystone Metals Recovery Inc. | Metal chlorides and metals obtained from metal oxide containing materials |
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US2721626A (en) * | 1951-12-15 | 1955-10-25 | Du Pont | Cooling and separating by condensation of hot gaseous suspensions |
US2817416A (en) * | 1954-01-28 | 1957-12-24 | California Research Corp | Liquid phthalic anhydride recovery |
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US2803311A (en) * | 1955-04-20 | 1957-08-20 | Montedison Spa | Process for separating pure, crystalline maleic anhydride directly from gaseous mixtures containing same |
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US3930800A (en) * | 1971-09-07 | 1976-01-06 | Aluminum Company Of America | Fluidized bed desubliming apparatus for recovery of aluminum chloride |
US4478600A (en) * | 1971-09-14 | 1984-10-23 | Aluminum Company Of America | Process for recovery of aluminum chloride |
US3952022A (en) * | 1973-01-16 | 1976-04-20 | Rhone-Progil | Method of condensing phthalic anhydride |
JPS5339877B2 (en) * | 1973-10-02 | 1978-10-24 | ||
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US4502871A (en) * | 1983-02-01 | 1985-03-05 | Gca Corporation | Apparatus and method for separating wax from an entrainer gas |
US5019137A (en) * | 1984-09-14 | 1991-05-28 | A. Ahlstrom Corporation | Method for cleaning gases containing condensable components |
US5032143A (en) * | 1987-05-08 | 1991-07-16 | A. Ahlstrom Corporation | Method and apparatus for treating process gases |
US4941895A (en) * | 1989-08-23 | 1990-07-17 | Amoco Corporation | Process for the continuous separation of maleic anhydride from process gases |
EP0537473A1 (en) * | 1991-10-17 | 1993-04-21 | Messer Griesheim Gmbh | Process for the recovery of solvants from waste air or gas |
FR2836059A1 (en) * | 2002-02-19 | 2003-08-22 | Ensmse | Continuous recovery process, e.g. for volatile organics, involves condensing or solidifying fraction from gaseous flow |
US20070224109A1 (en) * | 2006-03-23 | 2007-09-27 | Keystone Metals Recovery Inc. | Metal chlorides and metals obtained from metal oxide containing materials |
US9315382B2 (en) | 2006-03-23 | 2016-04-19 | Keystone Metals Recovery Inc. | Metal chlorides and metals obtained from metal oxide containing materials |
RU2477643C2 (en) * | 2007-12-23 | 2013-03-20 | Юниверсити Оф Дзе Уитвотерсранд, Йоханнесбург | Gas cleaning |
EP2408540A2 (en) * | 2009-03-16 | 2012-01-25 | Brigham Young University | Methods and systems for separating condensable vapors from gases |
EP2408540A4 (en) * | 2009-03-16 | 2014-11-26 | Sustainable Energy Solutions Llc | Methods and systems for separating condensable vapors from gases |
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