GB951260A - Method for regenerating a molecular sieve adsorbent - Google Patents
Method for regenerating a molecular sieve adsorbentInfo
- Publication number
- GB951260A GB951260A GB3812160A GB3812160A GB951260A GB 951260 A GB951260 A GB 951260A GB 3812160 A GB3812160 A GB 3812160A GB 3812160 A GB3812160 A GB 3812160A GB 951260 A GB951260 A GB 951260A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pressure
- column
- desorbing agent
- vapour
- molecular sieve
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G25/00—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents
- C10G25/02—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents with ion-exchange material
- C10G25/03—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents with ion-exchange material with crystalline alumino-silicates, e.g. molecular sieves
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/34—Regenerating or reactivating
- B01J20/3408—Regenerating or reactivating of aluminosilicate molecular sieves
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Analytical Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A molecular sieve adsorbent that contains adsorbed material is regenerated by contacting the adsorbent with a condensable desorbing agent vapour, increasing the partial pressure of said desorbing agent in contact with the molecular sieve within the range of 0.01 to 0.98 times the vapour pressure of the desorbing agent at the particular temperature employed to cause condensation of the desorbing agent substantially only within the molecular seive channels under the influence of the capillary condensation effect, and thereafter imposing conditions of temperature and pressure on the molecular sieves to cause revaporization and removal of such condensed desorbing agent. This method can be used in molecular sieve separation of many types of organic mixtures e.g. 2-butene from isoprene. The 2-butene/isoprene mixture is passed in the liquid or vapour phase into a column of molecular sieves e.g. as pellets, usually at atmospheric pressure and ambient temperature. Unadsorbed percolate is collected as one product of the separation until or just before the preferentially adsorbed material begins to appear in the percolate. The occluded material remaining in the column is withdrawn from the bottom and is recycled to the next separation phase. Regeneration of the column is then effected by contacting the sieve with the desorbent vapour n-butane until the pressure in the column is just below the pressure at which the desorbent vapour will condense. After a sufficient quantity has condensed the pressure on the column is reduced causing vaporization of the desorbing agent and removal of adsorbed impurities. The procedure of condensing the desorbing agent and revaporization should be repeated, preferably at least 3 times. The column is then purged with an inert gas, preferably at sub-atmospheric pressure and/or elevated temperature. The preferred desorbing agents are straight chain paraffins; they should be inert, should not polymerize, isomerize or decompose under the conditions used and it should be miscible with the material to be adsorbed. Specification 548,905 is referred to.ALSO:A molecular sieve adsorbent that contains adsorbed material is regenerated by contacting the adsorbent with a condensable desorbing agent vapour, increasing the partial pressure of said desorbing agent in contact with the molecular sieve within the range of 0,01-0,98 times the vapour pressure of the desorbing agent at the particular temperature employed to cause condensation of the desorbing agent substantially only within the molecular sieve channels under the influence of the capillary condensation effect, and thereafter imposing conditions of temperature and pressure on the molecular sieves to cause revaporization and removal of such condensed desorbing agent. This method can be used in molecular sieve separation of many types of organic mixtures, e.g. 2-butene from isoprene. The 2-butene/isoprene mixture is passed in the liquid or vapour phase into a column of molecular sieves, e.g. as pellets, usually at atmospheric pressure and ambient temperature. Unadsorbed percolate is collected as one product of the separation until or just before the preferentially adsorbed material begins to appear in the percolate. The occluded material remaining in the column is withdrawn from the bottom and is recycled to the next separation phase. Regeneration of the column is then effected by contacting the sieve with the desorbent vapour n-butane until the pressure in the column is just below the pressure at which the desorbent vapour will condense. After a sufficient quantity has condensed the pressure on the column is reduced causing vaporization of the desorbing agent and removal of adsorbed impurities. The procedure of condensing the desorbing agent and revaporization should be repeated, preferably at least three times. The column is then purged with an inert gas, preferably at sub-atmospheric pressure and/or elevated temperature. The preferred desorbing agents are straight chain paraffins which should be inert, should not polymerize, isomerize or decompose under the conditions used and should be miscible with the material to be adsorbed. Specification 548,905 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85203459A | 1959-11-10 | 1959-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB951260A true GB951260A (en) | 1964-03-04 |
Family
ID=25312346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3812160A Expired GB951260A (en) | 1959-11-10 | 1960-11-07 | Method for regenerating a molecular sieve adsorbent |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB951260A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108745276A (en) * | 2018-04-18 | 2018-11-06 | 南京工业大学 | Preparation method of mixed forming lithium ion adsorbent |
-
1960
- 1960-11-07 GB GB3812160A patent/GB951260A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108745276A (en) * | 2018-04-18 | 2018-11-06 | 南京工业大学 | Preparation method of mixed forming lithium ion adsorbent |
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