GB1004679A - Recovery of hydrogen chloride and unreacted propylene from propylene chlorination reaction product mixture - Google Patents
Recovery of hydrogen chloride and unreacted propylene from propylene chlorination reaction product mixtureInfo
- Publication number
- GB1004679A GB1004679A GB2123762A GB2123762A GB1004679A GB 1004679 A GB1004679 A GB 1004679A GB 2123762 A GB2123762 A GB 2123762A GB 2123762 A GB2123762 A GB 2123762A GB 1004679 A GB1004679 A GB 1004679A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propylene
- hcl
- mol
- via line
- mixture
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B7/00—Halogens; Halogen acids
- C01B7/01—Chlorine; Hydrogen chloride
- C01B7/07—Purification ; Separation
- C01B7/0706—Purification ; Separation of hydrogen chloride
- C01B7/0731—Purification ; Separation of hydrogen chloride by extraction
- C01B7/0737—Purification ; Separation of hydrogen chloride by extraction hydrogen chloride being extracted
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/005—Processes comprising at least two steps in series
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/11—Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
<PICT:1004679/C4-C5/1> Propylene is recovered from the reaction mixture from the thermal chlorination of propylene by (A) separating the organic chlorides from the mixture, and (B) bringing the resulting mixture of HCl and propylene into contact with azeotropic aqueous HCl solution to absorb the HCl, with consequent separation of some of the propylene; (C) stripping residual propylene from the resulting aqueous solution and recycling to step (B); (D) separating anhydrous HCl from the rich aqueous solution leaving an azeotropic aqueous HCl solution which is fed back to step (B). In the Figure, the reaction product mixture, having the proportions 1 mol. allyl choloride, 1 to 6.7 mol. propylene, and 0.5 to 1.7 mol. HCl, passes from reactor 12 through cooler 14 via line 15 to fractionating column 16, whence crude allyl chloride leaves at 18. Propylene reflux, which may be added in the proportion of 100 to 400 mol. per 90 mol. allyl chloride, enters via line 17, and a mixture of propylene and HCl is passed via line 19 to absorber 20, which may operate adiabatically, where it meets water from line 21 and azeotropic aqueous HCl solution from line 29. Wet propylene vapour leaves at 22. Rich aqueous HCl solution containing some propylene passes via line 23 t propylene stripper 24 which is heated, and the stripped propylene vapour is returned via 25 to absorber 20. The rich HCl solution passes via 26 to HCl stripper 27. Anhydrous HCl leaves at 28, and the residual azeotropic HCl solution is recycled via line 29 to absorber 20. The wet propylene from 22 is caustic scrubbed, compressed and condensed, and is recycled via 11 to reactor 12 or introduced as reflux into column 16.ALSO:<FORM:1004679/C2/1> Alkyl chloride formed by the thermal chlorination of propylene is separated from HCl and propylene in the reaction product mixture. In the figure, the reaction product mixture having the proportions 1 mol. allyl chloride, 1 to 6-7 mol. propylene, and 0.5 to 1.7 mol. HCl, passes from reactor 12 through cooler 14 via line 15 to fractionating column 16, whence crude allyl chloride leaves at 18. Propylene reflux, which may be added in the proportion of 100 to 400 mol. per 90 mol. allyl chloride, enters via line 17. A mixture of propylene and HCl passes via line 19 to apparatus for recovery of the HCl and the propylene; recovered propylene may be recycled via 11 to reactor 12 or introduced as reflux into column 16.ALSO:<PICT:1004679/C1/1> Hydrogen chloride and propylene are recovered from the reaction mixture from the thermal chlorination of propylene by (A) separating the organic chlorides from the mixture, and (B) bringing the resulting mixture of HCl and propylene into contact with azeotropic aqueous HCl solution to absorb the HCl, with consequent separation of some of the propylene; (C) stripping residual propylene from the resulting aqueous solution and recycling to step (B); (D) separating anhydrous HCl from the rich aqueous solution leaving an azeotropic aqueous HCl solution which is fed back to step (B). In the Figure, the reaction product mixture, having the proportions 1 mol. allyl chloride, 1 to 6.7 mol. propylene, and 0.5 to 1.7 mol. allyl chloride, 1 to 6.7 mol. propylene, and 0.5 to 1.7 mol. HCl, passes from reactor 12 through cooler 14 via line 15 to fractionating column 16, whence crude allyl chloride leaves at 18. Propylene reflux, which may be added in the proportion of 100 to 400 mol. per 90 mol. allyl chloride, enters via line 17, and a mixture of propylene and HCl is passed via line 19 to absorber 20, which may operate adiabatically, where it meets water from line 21 and azeotropic aqueous HCl solution from line 29. Wet propylene vapour leaves at 22. Rich aqueous HCl solution containing some propylene passes via line 23 to propylene stripper 24 which is heated, and the stripped propylene vapour is returned via 25 to absorber 20. The rich HCl solution passes via 26 to HCl stripper 27. Anhydrous HCl leaves at 28, and the residual azeotropic HCl solution is recycled via line 29 to absorber 20. The wet propylene from 22 is caustic scrubbed, compressed and condensed, and is recycled via 11 to reactor 12 or introduced as refluxed into column 16.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11441661A | 1961-06-02 | 1961-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1004679A true GB1004679A (en) | 1965-09-15 |
Family
ID=22355046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2123762A Expired GB1004679A (en) | 1961-06-02 | 1962-06-01 | Recovery of hydrogen chloride and unreacted propylene from propylene chlorination reaction product mixture |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE618179A (en) |
CH (1) | CH413816A (en) |
DE (1) | DE1200286B (en) |
GB (1) | GB1004679A (en) |
LU (1) | LU41796A1 (en) |
NL (1) | NL279181A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011105637A (en) * | 2009-11-17 | 2011-06-02 | Sumitomo Chemical Co Ltd | Method for producing allyl chloride and dichlorohydrin |
EP2368842A1 (en) * | 2008-12-03 | 2011-09-28 | Sumitomo Chemical Company, Limited | Hydrochloric acid purifying method |
EP2371763A1 (en) * | 2008-12-03 | 2011-10-05 | Sumitomo Chemical Company, Limited | Hydrochloric acid purifying method |
EP2949622A1 (en) * | 2014-05-27 | 2015-12-02 | Covestro Deutschland AG | Method for processing hydrogen chloride from isocyanate production |
-
0
- BE BE618179D patent/BE618179A/xx unknown
- NL NL279181D patent/NL279181A/xx unknown
-
1962
- 1962-05-29 LU LU41796D patent/LU41796A1/xx unknown
- 1962-06-01 GB GB2123762A patent/GB1004679A/en not_active Expired
- 1962-06-02 DE DES79755A patent/DE1200286B/en active Pending
- 1962-06-02 CH CH669262A patent/CH413816A/en unknown
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2368842A1 (en) * | 2008-12-03 | 2011-09-28 | Sumitomo Chemical Company, Limited | Hydrochloric acid purifying method |
EP2371763A1 (en) * | 2008-12-03 | 2011-10-05 | Sumitomo Chemical Company, Limited | Hydrochloric acid purifying method |
EP2368842A4 (en) * | 2008-12-03 | 2012-08-01 | Sumitomo Chemical Co | Hydrochloric acid purifying method |
EP2371763A4 (en) * | 2008-12-03 | 2012-08-01 | Sumitomo Chemical Co | Hydrochloric acid purifying method |
JP2011105637A (en) * | 2009-11-17 | 2011-06-02 | Sumitomo Chemical Co Ltd | Method for producing allyl chloride and dichlorohydrin |
EP2501665A1 (en) * | 2009-11-17 | 2012-09-26 | Sumitomo Chemical Company, Limited | Methods for producing allyl chloride and dichlorohydrin |
EP2501665A4 (en) * | 2009-11-17 | 2013-04-24 | Sumitomo Chemical Co | Methods for producing allyl chloride and dichlorohydrin |
EP2949622A1 (en) * | 2014-05-27 | 2015-12-02 | Covestro Deutschland AG | Method for processing hydrogen chloride from isocyanate production |
Also Published As
Publication number | Publication date |
---|---|
LU41796A1 (en) | 1963-11-29 |
CH413816A (en) | 1966-05-31 |
DE1200286B (en) | 1965-09-09 |
BE618179A (en) | 1962-11-28 |
NL279181A (en) |
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