JPH0225893B2 - - Google Patents
Info
- Publication number
- JPH0225893B2 JPH0225893B2 JP57182624A JP18262482A JPH0225893B2 JP H0225893 B2 JPH0225893 B2 JP H0225893B2 JP 57182624 A JP57182624 A JP 57182624A JP 18262482 A JP18262482 A JP 18262482A JP H0225893 B2 JPH0225893 B2 JP H0225893B2
- Authority
- JP
- Japan
- Prior art keywords
- alkali metal
- chloroprene
- dichlorobutene
- reaction
- aqueous solution
- 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 - Lifetime
Links
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims description 46
- 238000006243 chemical reaction Methods 0.000 claims description 30
- XVEASTGLHPVZNA-UHFFFAOYSA-N 3,4-dichlorobut-1-ene Chemical compound ClCC(Cl)C=C XVEASTGLHPVZNA-UHFFFAOYSA-N 0.000 claims description 26
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- 239000008346 aqueous phase Substances 0.000 claims description 20
- 239000007864 aqueous solution Substances 0.000 claims description 18
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 16
- 239000012074 organic phase Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 11
- 239000012071 phase Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 9
- 238000001704 evaporation Methods 0.000 claims description 7
- 238000007033 dehydrochlorination reaction Methods 0.000 claims description 6
- 230000008020 evaporation Effects 0.000 claims description 5
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 claims description 2
- 239000007809 chemical reaction catalyst Substances 0.000 claims 1
- 238000000034 method Methods 0.000 description 23
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 16
- 229920000642 polymer Polymers 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 238000004821 distillation Methods 0.000 description 11
- 239000006227 byproduct Substances 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical compound CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- AQZSPJRLCJSOED-UHFFFAOYSA-M trimethyl(octyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(C)C AQZSPJRLCJSOED-UHFFFAOYSA-M 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57182624A JPS5970626A (ja) | 1982-10-18 | 1982-10-18 | クロロプレンの製造法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57182624A JPS5970626A (ja) | 1982-10-18 | 1982-10-18 | クロロプレンの製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5970626A JPS5970626A (ja) | 1984-04-21 |
JPH0225893B2 true JPH0225893B2 (enrdf_load_stackoverflow) | 1990-06-06 |
Family
ID=16121538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57182624A Granted JPS5970626A (ja) | 1982-10-18 | 1982-10-18 | クロロプレンの製造法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5970626A (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5978128A (ja) * | 1982-10-26 | 1984-05-04 | Denki Kagaku Kogyo Kk | クロロプレンを製造する方法 |
FR2710056B1 (fr) * | 1993-09-17 | 1995-12-01 | Enichem Elastomeres France | Procédé de déshydrochloration du 3,4-dichloro-1-butène en chloroprène. |
-
1982
- 1982-10-18 JP JP57182624A patent/JPS5970626A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5970626A (ja) | 1984-04-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4907835B2 (ja) | フッ素化アルカン酸の精製方法 | |
CA1269995A (en) | Process for the preparation of liquid 2-hydroxy- methylthiobutyric acid | |
JPH051776B2 (enrdf_load_stackoverflow) | ||
JPH0225893B2 (enrdf_load_stackoverflow) | ||
JP2017518998A5 (enrdf_load_stackoverflow) | ||
JPH10182593A (ja) | メチオニンの製造方法 | |
US6392084B1 (en) | Method for production of organic fluorine compound | |
US4400325A (en) | Process for the preparation of pure, saturated perfluoroalkane-1-carboxylic acids from 1-iodoperfluoroalkanes | |
JPH11100375A (ja) | (メタ)アクリロイルモルホリンの製法 | |
JPH0354649B2 (enrdf_load_stackoverflow) | ||
JP2845745B2 (ja) | 高純度メタンスルホニルフロライドの製造法 | |
JPH0542460B2 (enrdf_load_stackoverflow) | ||
JP3013451B2 (ja) | ショ糖脂肪酸エステルの製造方法 | |
US5091057A (en) | Stripping process for water removal from alcohol | |
JPH0662482B2 (ja) | 1,1’―パーオキシジシクロヘキシルアミンの熱分解反応混合液からシクロヘキサノンを回収する方法 | |
US5043492A (en) | Method for producing hexabromocyclododecane | |
CN1196526C (zh) | 从水溶液中回收强酸的方法 | |
JPH0150213B2 (enrdf_load_stackoverflow) | ||
JPH07233104A (ja) | テトラフルオロエチレンの製造方法 | |
JP2756373B2 (ja) | 1,1,1−トリフルオロ−3−ニトロ−2−プロペンの製造方法 | |
CA1284153C (en) | Preparation of alkyl trifluroacetoacetate | |
JP4221782B2 (ja) | ジハロトリフルオロアセトンの精製方法 | |
JPH09143175A (ja) | プロピレンオキシドの回収方法 | |
JP2946944B2 (ja) | アルキルアミノフェノール類の製造方法 | |
JP3866872B2 (ja) | テレフタル酸ジメチルの回収方法 |