SU194088A1 - - Google Patents
Info
- Publication number
- SU194088A1 SU194088A1 SU1074163A SU1074163A SU194088A1 SU 194088 A1 SU194088 A1 SU 194088A1 SU 1074163 A SU1074163 A SU 1074163A SU 1074163 A SU1074163 A SU 1074163A SU 194088 A1 SU194088 A1 SU 194088A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dicyanbuten
- product
- acrylonitrile
- adiponitrile
- electrolysis
- Prior art date
Links
- 239000000047 product Substances 0.000 description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 8
- 238000005868 electrolysis reaction Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- -1 2-cyanoethyl adiponitrile Chemical compound 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- ZQOHAQBXINVHHC-HNQUOIGGSA-N (e)-hex-2-enedinitrile Chemical compound N#CCC\C=C\C#N ZQOHAQBXINVHHC-HNQUOIGGSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GIBPRDXIXACLKK-UHFFFAOYSA-N butane-1,1,4-tricarbonitrile Chemical compound N#CCCCC(C#N)C#N GIBPRDXIXACLKK-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007862 dimeric product Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- LNLFLMCWDHZINJ-UHFFFAOYSA-N hexane-1,3,6-tricarbonitrile Chemical compound N#CCCCC(C#N)CCC#N LNLFLMCWDHZINJ-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU194088A1 true SU194088A1 (enrdf_load_stackoverflow) |
Family
ID=
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118920018A (zh) * | 2024-10-11 | 2024-11-08 | 中国科学院大连化学物理研究所 | 一种锂离子电池隔膜的制备方法及其制备的隔膜和应用 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118920018A (zh) * | 2024-10-11 | 2024-11-08 | 中国科学院大连化学物理研究所 | 一种锂离子电池隔膜的制备方法及其制备的隔膜和应用 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US10370767B2 (en) | Process for preparing alcohols by electrochemical reductive coupling | |
| US3344046A (en) | Electrolytic preparation of organic carbonates | |
| CN110073036A (zh) | 过硫酸铵的制造方法 | |
| SU194088A1 (enrdf_load_stackoverflow) | ||
| US3941666A (en) | Process for the preparation of N-(α-alkoxyethyl)-carboxylic acid amides | |
| US3692643A (en) | Electrofluorination process using thioesters | |
| US3193574A (en) | Process for the preparation of adiponitrile by dimerization of acrylonitrile | |
| US3822306A (en) | Production of alpha-n-formylamino acid compounds | |
| US3413202A (en) | Electrolysis of di-olefinic compounds | |
| EP0018473B1 (de) | Verfahren zur Herstellung von beta-Alkoxy-acrylnitrilen, 3-Amino-acrylnitrilen und 2-Cyano-vinylestern | |
| SU415271A1 (ru) | Способ получения висмуторганических соединений | |
| US1163498A (en) | Manufacture of metallic amids, cyanamids, and cyanids. | |
| US4024033A (en) | Process for preparing cyanogen halides | |
| US3455986A (en) | Process for the reductive dimerization of alpha,beta-olefinic compounds | |
| US20080228009A1 (en) | Process for Preparing 1,1,4,4-Tetraalkoxybut-2-Ene Derivatives | |
| US3658667A (en) | Electrolyte reduction of ozonolysis products | |
| EP0228181B1 (en) | Process for producing m-hydroxybenzyl alcohol | |
| RU2803889C1 (ru) | Способ получения 4-хлор-2-аминофенола | |
| US3411997A (en) | Electrolytic process for preparing nlower acyloxymethyl-n-hydrocabyl lower acylamides and certain derivatives thereof | |
| US3477923A (en) | Electrochemical hydrodimerization of acrylonitrile | |
| SU178807A1 (enrdf_load_stackoverflow) | ||
| SU379086A1 (ru) | Способ получения адипонитрила | |
| SU186398A1 (enrdf_load_stackoverflow) | ||
| DE2842760A1 (de) | Verfahren zur herstellung von n-(alpha- methoxy-alkyl)-urethanen und n-(alpha- methoxy-alkyl)-urethane | |
| WO1990014448A1 (en) | Electrolytic reductive coupling of quaternary ammonium compounds |