JPH0227979B2 - - Google Patents
Info
- Publication number
- JPH0227979B2 JPH0227979B2 JP57155738A JP15573882A JPH0227979B2 JP H0227979 B2 JPH0227979 B2 JP H0227979B2 JP 57155738 A JP57155738 A JP 57155738A JP 15573882 A JP15573882 A JP 15573882A JP H0227979 B2 JPH0227979 B2 JP H0227979B2
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- amine
- tertiary amines
- carbon atoms
- produced
- 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
- 150000003512 tertiary amines Chemical class 0.000 claims description 36
- 239000003054 catalyst Substances 0.000 claims description 34
- 150000001412 amines Chemical class 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 14
- 238000004821 distillation Methods 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 150000001336 alkenes Chemical class 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
- 239000010948 rhodium Substances 0.000 claims description 9
- 150000001298 alcohols Chemical class 0.000 claims description 8
- 229910052703 rhodium Inorganic materials 0.000 claims description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 6
- 229910052707 ruthenium Inorganic materials 0.000 claims description 6
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 229920000223 polyglycerol Polymers 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 150000003335 secondary amines Chemical class 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 230000018044 dehydration Effects 0.000 claims description 2
- 238000006297 dehydration reaction Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 238000004064 recycling Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 26
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 12
- 229940069096 dodecene Drugs 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- GFKYEYVYVGMLQL-UHFFFAOYSA-N n,n-diethyltridecan-1-amine Chemical compound CCCCCCCCCCCCCN(CC)CC GFKYEYVYVGMLQL-UHFFFAOYSA-N 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 230000006866 deterioration Effects 0.000 description 6
- 238000011084 recovery Methods 0.000 description 6
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 5
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229940105990 diglycerin Drugs 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005674 electromagnetic induction Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000000622 liquid--liquid extraction Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- DXFFQWDOIJVGNR-UHFFFAOYSA-N n,n-diethylundecan-1-amine Chemical compound CCCCCCCCCCCN(CC)CC DXFFQWDOIJVGNR-UHFFFAOYSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- Y02P20/584—Recycling of 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 |
---|---|---|---|
JP57155738A JPS5944344A (ja) | 1982-09-07 | 1982-09-07 | 第三級アミン類の製造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57155738A JPS5944344A (ja) | 1982-09-07 | 1982-09-07 | 第三級アミン類の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5944344A JPS5944344A (ja) | 1984-03-12 |
JPH0227979B2 true JPH0227979B2 (pl) | 1990-06-20 |
Family
ID=15612359
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57155738A Granted JPS5944344A (ja) | 1982-09-07 | 1982-09-07 | 第三級アミン類の製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5944344A (pl) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60258145A (ja) * | 1984-06-02 | 1985-12-20 | Mitsubishi Petrochem Co Ltd | 第三級アミンの製造方法 |
KR910004884B1 (ko) * | 1989-02-01 | 1991-07-15 | 한국식품개발연구원 | 유지류의 산화억제방법 |
DE4334809A1 (de) * | 1993-10-13 | 1995-04-20 | Hoechst Ag | Verfahren zur Herstellung sekundärer oder tertiärer Amine |
-
1982
- 1982-09-07 JP JP57155738A patent/JPS5944344A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5944344A (ja) | 1984-03-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2595096A (en) | Synthesis of alcohol from olefins, carbon monoxide, and hydrogen | |
US4302298A (en) | Process for isolating methyl tert-butyl ether from the reaction products of methanol with a C4 hydrocarbon cut containing isobutene | |
US2526676A (en) | Process for producing acrylonitrile | |
JP4061023B2 (ja) | n−プロパノールを製造する方法 | |
US5292917A (en) | Process for purifying dimethyl carbonate | |
US3470252A (en) | Production of secondary alkyl primary amines from normal paraffins | |
CA2014152C (en) | Process for the preparation of an alkyl methacrylate | |
KR100317920B1 (ko) | 올리고머생성물에서촉매제를제거하는방법 | |
JPH0227979B2 (pl) | ||
CN101415669B (zh) | 甲基丙烯酸甲酯的制造方法 | |
JPS6051451B2 (ja) | 第3級ブチルアルコ−ルの製造法 | |
EP0501374B1 (en) | Process for purifying dimethyl carbonate | |
US4284837A (en) | Process for recovery of an aliphatic diol oligomerization solvent | |
US4094916A (en) | Process for the production of endo-endo hexacyclic dimer of norbornadiene | |
JP2005501807A5 (pl) | ||
US2542488A (en) | Production of olefins | |
US3651165A (en) | Method for recovery and purification of isobutylene | |
US5081286A (en) | Process for the preparation of an alkyl methacrylate | |
CA1077066A (en) | Process for the direct separation of isobutylene from mixtures of hydrocarbons | |
JPH0149134B2 (pl) | ||
US4094917A (en) | Process for the production of exo-exo hexacyclic dimer of norbornadiene | |
US4258223A (en) | Process for the preparation of tertiary butyl alcohol | |
KR0186001B1 (ko) | 2급-부틸벤젠의 제조방법 | |
JPH07258210A (ja) | イソブタンの酸化方法 | |
JPS6412263B2 (pl) |