JPH0377181B2 - - Google Patents
Info
- Publication number
- JPH0377181B2 JPH0377181B2 JP24968983A JP24968983A JPH0377181B2 JP H0377181 B2 JPH0377181 B2 JP H0377181B2 JP 24968983 A JP24968983 A JP 24968983A JP 24968983 A JP24968983 A JP 24968983A JP H0377181 B2 JPH0377181 B2 JP H0377181B2
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- lower alkyl
- acid ester
- saturated fatty
- acid lower
- 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
- -1 Alkylene glycol Chemical compound 0.000 claims description 33
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 24
- 238000000926 separation method Methods 0.000 claims description 19
- 125000005907 alkyl ester group Chemical group 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 9
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 5
- 230000003068 static effect Effects 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 230000003472 neutralizing effect Effects 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 238000006277 sulfonation reaction Methods 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000010409 thin film Substances 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
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000008054 sulfonate salts Chemical class 0.000 description 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000004665 fatty acids Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24968983A JPS60139662A (ja) | 1983-12-27 | 1983-12-27 | 不飽和脂肪酸低級アルキルエステルスルホン酸塩の製造法 |
EP84304246A EP0130753B1 (en) | 1983-07-01 | 1984-06-22 | Process for producing sulfonate of unsaturated fatty acid ester |
DE8484304246T DE3468020D1 (en) | 1983-07-01 | 1984-06-22 | Process for producing sulfonate of unsaturated fatty acid ester |
US06/626,081 US4545939A (en) | 1983-07-01 | 1984-06-29 | Process for producing sulfonate of unsaturated fatty acid ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24968983A JPS60139662A (ja) | 1983-12-27 | 1983-12-27 | 不飽和脂肪酸低級アルキルエステルスルホン酸塩の製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60139662A JPS60139662A (ja) | 1985-07-24 |
JPH0377181B2 true JPH0377181B2 (en, 2012) | 1991-12-09 |
Family
ID=17196735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24968983A Granted JPS60139662A (ja) | 1983-07-01 | 1983-12-27 | 不飽和脂肪酸低級アルキルエステルスルホン酸塩の製造法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60139662A (en, 2012) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6379865A (ja) * | 1986-09-25 | 1988-04-09 | Nippon Mining Co Ltd | パラフインの光スルホキシ化反応混合液からの硫酸塩の除去方法 |
-
1983
- 1983-12-27 JP JP24968983A patent/JPS60139662A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS60139662A (ja) | 1985-07-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2906298B2 (ja) | 第二アルキル硫酸塩含有界面活性剤組成物の製造方法 | |
EP0130753B1 (en) | Process for producing sulfonate of unsaturated fatty acid ester | |
US2457257A (en) | Separation of oxygeated compound with bisulfite adducts | |
US2383596A (en) | Method of treating fatty glycerides | |
GB2146638A (en) | Producing fatty acids from lower alkyl esters of fatty acids | |
JPH0443904B2 (en, 2012) | ||
US2525702A (en) | Purification of oil | |
JPH0377181B2 (en, 2012) | ||
JPS6126779B2 (en, 2012) | ||
JP2003507444A (ja) | 脂肪酸エステルの脂肪酸への非腐食性の接触加水分解 | |
US2572467A (en) | Concentration and recovery of carotenoid pigments from palm oil | |
JPH0776533A (ja) | α−メチルスチレン類の不飽和二量体の製造法 | |
US2885446A (en) | Process for improving color of oil-soluble alcohols | |
US5281366A (en) | Process for the preparation of secondary alkyl sulfate-containing surfactant compositions | |
US1954506A (en) | Manufacture of alcohols | |
US2078638A (en) | Purification of sulphonation products | |
KR100278752B1 (ko) | 이차 알킬 설페이트를 포함하는 계면활성제 조성물의 제조 방법 | |
US2108755A (en) | Process for purification of sulphonation products | |
US5290484A (en) | Process for the preparation of secondary alkyl sulfate-containing surfactant compositions | |
US2207385A (en) | Preparation of vitamin concentrate | |
US3872142A (en) | Method of purifying alkali metal soaps of synthetic fatty acids | |
US3578689A (en) | Ester purification process | |
US2499877A (en) | Extraction of unsaponifiables from wool grease | |
US3865861A (en) | Sulphation of secondary alcohols | |
US3505367A (en) | Process for purifying raw sulfonates |