GB989073A - Adsorption separation process - Google Patents
Adsorption separation processInfo
- Publication number
- GB989073A GB989073A GB32933/61A GB3293361A GB989073A GB 989073 A GB989073 A GB 989073A GB 32933/61 A GB32933/61 A GB 32933/61A GB 3293361 A GB3293361 A GB 3293361A GB 989073 A GB989073 A GB 989073A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bed
- adsorption
- pressure
- impurity
- stream
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- C07C7/00—Purification; Separation; Use of additives
- C07C7/12—Purification; Separation; Use of additives by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers
- C07C7/13—Purification; Separation; Use of additives by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers by molecular-sieve technique
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
- B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
- B01D53/047—Pressure swing adsorption
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- C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
- C01B13/02—Preparation of oxygen
- C01B13/0229—Purification or separation processes
- C01B13/0248—Physical processing only
- C01B13/0259—Physical processing only by adsorption on solids
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- C01B3/50—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification
- C01B3/56—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification by contacting with solids; Regeneration of used solids
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- B01D2253/102—Carbon
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- Inorganic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
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- Separation Of Gases By Adsorption (AREA)
Abstract
989,073. Molecular sieve separation process. UNION CARBIDE CORPORATION. Sept. 14, 1961 [Sept. 16, 1960; Oct. 5, 1960], No.32933/61. Heading B1L. A feed fluid gaseous or liquid stream containing an admixture of impurity and product fluid is purified by introducing the stream into the inlet end of an adsorption zone, which contains a bed of particulate zeolitic molecular sieve, at an increased pressure, thereby adsorbing impurity in the sieve and trapping a part of the feed fluid stream in the voids of the sieve. An impurity adsorption front is established during this adsorption step, which advances to a predetermined location within the adsorption zone, whereupon the introduction of the feed fluid stream is terminated. The product fluid trapped in the voids is removed by a cocurrent depressurizing step during which time the pressure in the adsorption zone decreases and the impurity adsorption front moves to the discharge end of the adsorption zone. The impurity is then removed from the adsorbent by any known desorption method. The desorbed adsorption zone is then repressurized to the initial higher pressure. When the repressurization stream has an impurity partial pressure not higher than that permissible in the product, repressurization is countercurrent to the adsorption flow direction. When the impurity partial pressure of the repressurization stream is greater than this, the repressurization flow direction should be cocurrent to the adsorption flow direction. Up to four adsorption zones may be used in the process, the successive-adsorption, cocurrent depressurizing, desorption and repressurizing steps being carried out consecutively in each zone. The adsorption zones may comprise one or two beds of molecular sieve. Referring now to Fig. 3, the feed gas stream at a first higher pressure is directed through heat exchanger 11, and passed into bed A. The effluent which is purified prdouct gas is passed through conduit 17 to storage. Adsorption is continued in bed A until breakthrough point is reached, when the flow to bed A is shut off and redirected to bed B. Valves 18 and 28 are opened cocurrently depressurizing bed A, the effluent from bed A is passed, via conduit 26, to bed D which thus functions as an unused portion of bed A into which the impurity adsorption front now moves. The effluent from adsorption bed D is a purified product at a lower pressure than the adsorption step pressure and is directed through conduits 30 and 31 to repressurize adsorption bed C, which had previously completed a desorption step. When the pressure between beds C and D equalizes, passaeg of gas between them is terminated and bed C is further repressurized by passing feed gas together with the effluent from bed D (via reservoir 34) through thermocompressor 40 to bed C. The pressure in bed A which is still connected to bed D is also decreased by this method, thus completing the cocurrent depressurizing step for bed A. At this point, bed D is vented via conduit 44 to atmospheric pressure. When the pressure in bed D approaches atmospheric, bed A is desorbed at a yet lower pressure through conduit 41, eductor 48 and conduit 49. The eductor 48 at the same time evacuates and desorbs bed D to a subatmospheric pressure through conduit 29 and 49. When adsorbent beds A and D are finally desorbed, the feed gas stream is directed to bed C. Meanwhile adsorbent bed A is being repressurized and adsorbent bed B is being cocurrently depressurized and desorbed. In this method the adsorbent bed D is used to provide the unused molecular sieve capacity required during the cocurrent depressurization stroke for each of the adsorbent beds A, B and C thereby completing for each bed the adsorption zone.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US56514A US3176445A (en) | 1960-09-16 | 1960-09-16 | Method of separating gas mixtures by adsorption |
US6070960A | 1960-10-05 | 1960-10-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB989073A true GB989073A (en) | 1965-04-14 |
Family
ID=26735395
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32933/61A Expired GB989073A (en) | 1960-09-16 | 1961-09-14 | Adsorption separation process |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB989073A (en) |
NL (2) | NL145769B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0022315A1 (en) * | 1979-06-08 | 1981-01-14 | John Zink Company | Process and apparatus for recovering hydrocarbons from air-hydrocarbon vapor mixtures |
FR2520250A1 (en) * | 1982-01-26 | 1983-07-29 | Taiyo Sanso Co Ltd | PROCESS AND APPARATUS FOR THE PURIFICATION OF GAS OR EXTRACTION THEREOF FROM A MIXTURE COMPRISING THE SAME |
-
0
- NL NL266306D patent/NL266306A/xx unknown
-
1961
- 1961-06-23 NL NL61266306A patent/NL145769B/en not_active IP Right Cessation
- 1961-09-14 GB GB32933/61A patent/GB989073A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0022315A1 (en) * | 1979-06-08 | 1981-01-14 | John Zink Company | Process and apparatus for recovering hydrocarbons from air-hydrocarbon vapor mixtures |
FR2520250A1 (en) * | 1982-01-26 | 1983-07-29 | Taiyo Sanso Co Ltd | PROCESS AND APPARATUS FOR THE PURIFICATION OF GAS OR EXTRACTION THEREOF FROM A MIXTURE COMPRISING THE SAME |
Also Published As
Publication number | Publication date |
---|---|
NL145769B (en) | 1975-05-15 |
NL266306A (en) | 1900-01-01 |
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