GB857087A - Process for the manufacture of vinyl chloride - Google Patents
Process for the manufacture of vinyl chlorideInfo
- Publication number
- GB857087A GB857087A GB27466/57A GB2746657A GB857087A GB 857087 A GB857087 A GB 857087A GB 27466/57 A GB27466/57 A GB 27466/57A GB 2746657 A GB2746657 A GB 2746657A GB 857087 A GB857087 A GB 857087A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloride
- mixture
- mixtures
- carbon tetrachloride
- acetylene
- 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
- 238000000034 method Methods 0.000 title abstract 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 abstract 11
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 8
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 5
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 abstract 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 229910052797 bismuth Inorganic materials 0.000 abstract 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 239000001294 propane Substances 0.000 abstract 2
- 229950011008 tetrachloroethylene Drugs 0.000 abstract 2
- XFNULPWIQORGFM-UHFFFAOYSA-N 1,1,2,2-tetrachloroethene;tetrachloromethane Chemical group ClC(Cl)(Cl)Cl.ClC(Cl)=C(Cl)Cl XFNULPWIQORGFM-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- UJOKUMXIAVXKPS-UHFFFAOYSA-N [Zn].[V].[Mg] Chemical compound [Zn].[V].[Mg] UJOKUMXIAVXKPS-UHFFFAOYSA-N 0.000 abstract 1
- LGWKODHZVOMBNJ-UHFFFAOYSA-N acetylene chloroethene Chemical group C(=C)Cl.C#C LGWKODHZVOMBNJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 abstract 1
- 229910052788 barium Inorganic materials 0.000 abstract 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 229910052793 cadmium Inorganic materials 0.000 abstract 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 1
- 238000005336 cracking Methods 0.000 abstract 1
- 229960003750 ethyl chloride Drugs 0.000 abstract 1
- 238000005194 fractionation Methods 0.000 abstract 1
- 239000008246 gaseous mixture Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 229940050176 methyl chloride Drugs 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052712 strontium Inorganic materials 0.000 abstract 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 abstract 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/08—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
In a process for the manufacture of vinyl chloride acetylene is reacted in the presence of a catalyst known to be suitable for the addition of hydrogen chloride to acetylene with a gaseous mixture consisting substantially of hydrogen chloride and chlorinated alkanes in the vapour state. Mixtures of hydrogen chloride and low boiling chloralkanes such as methyl or ethyl chloride or mixtures of tetra chlorethylene, carbon tetrachloride and hydrogen chloride obtained by chlorinating methane at high temperatures or similar mixtures obtained by simultaneously chlorinating and partially cracking ethane and propane may be employed in the process. Catalysts specified include mercury chloride or vanadate, compounds of bismuth, antimony, barium, strontium, calcium, magnesium vanadium zinc or iron such as the chlorides or mixtures thereof, e.g. mixtures of mercury chloride with alkali metal chlorides or activated carbon. Dissolved catalysts may be employed, e.g., cuprous or mercury chloride to which one or more compounds of metals of Group II-V or VII, e.g. compounds of zinc, cadmium, manganese, antimony or bismuth. An apparatus for carrying out the process is described with reference to a Figure (not shown). In examples: Vinyl chloride, carbon tetrachloride and some chloroform are obtained by reacting gaseous chlorine and methane, passing the reactor mixture with further methane through a reactor to eliminate traces of free chlorine and obtain a mixture of carbon tetrachloride and hydrogen chloride with some chloroform and methane and reacting such mixture with acetylene in the presence of active carbon impregnated with aqueous mercury chloride (1); and in a similar process a mixture of vinyl chloride, carbon tetrachloride tetrachlorethylene and hexachlorethane is obtained by heating a mixture of chlorine, propane, carbon tetrachloride and tetrachlorethylene, passing the products over heated active carbon, mixing the products with acetylene and reacting the mixture in the presence of active carbon impregnated with aqueous mercury chloride (2). The compounds of the reaction products may be obtained by fractionation. Specification 349,017 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE857087X | 1956-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB857087A true GB857087A (en) | 1960-12-29 |
Family
ID=6789476
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB27466/57A Expired GB857087A (en) | 1956-08-30 | 1957-08-30 | Process for the manufacture of vinyl chloride |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB857087A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102125830A (en) * | 2011-01-21 | 2011-07-20 | 李伟 | Mercury-free catalyst for use in production of chloroethylene by calcium carbide method |
| CN102675035A (en) * | 2012-06-11 | 2012-09-19 | 上海中科高等研究院 | Method for preparing vinyl chloride from acetylene and dichloroethane |
| CN104326866A (en) * | 2014-10-16 | 2015-02-04 | 中科易工(上海)化学科技有限公司 | Process for production of chloroethylene by acetylene and dichloroethane catalytic reforming |
| CN104326867A (en) * | 2014-10-16 | 2015-02-04 | 中科易工(上海)化学科技有限公司 | Separation and recovery method of chloroethylene in tail gas of process for production of chloroethylene by acetylene and dichloroethane mercury-free catalytic synthesis |
-
1957
- 1957-08-30 GB GB27466/57A patent/GB857087A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102125830A (en) * | 2011-01-21 | 2011-07-20 | 李伟 | Mercury-free catalyst for use in production of chloroethylene by calcium carbide method |
| CN102675035A (en) * | 2012-06-11 | 2012-09-19 | 上海中科高等研究院 | Method for preparing vinyl chloride from acetylene and dichloroethane |
| CN104326866A (en) * | 2014-10-16 | 2015-02-04 | 中科易工(上海)化学科技有限公司 | Process for production of chloroethylene by acetylene and dichloroethane catalytic reforming |
| CN104326867A (en) * | 2014-10-16 | 2015-02-04 | 中科易工(上海)化学科技有限公司 | Separation and recovery method of chloroethylene in tail gas of process for production of chloroethylene by acetylene and dichloroethane mercury-free catalytic synthesis |
| CN104326866B (en) * | 2014-10-16 | 2016-03-16 | 中科易工(上海)化学科技有限公司 | A kind of acetylene and ethylene dichloride catalytic reforming produce process for vinyl chloride |
| CN104326867B (en) * | 2014-10-16 | 2016-03-16 | 中科易工(上海)化学科技有限公司 | A kind of acetylene and ethylene dichloride catalyze and synthesize the separation and recovery method of vinylchlorid in process for vinyl chloride tail gas without mercury |
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