NO136457B - - Google Patents
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- Publication number
- NO136457B NO136457B NO4469/71A NO446971A NO136457B NO 136457 B NO136457 B NO 136457B NO 4469/71 A NO4469/71 A NO 4469/71A NO 446971 A NO446971 A NO 446971A NO 136457 B NO136457 B NO 136457B
- Authority
- NO
- Norway
- Prior art keywords
- reaction
- interesterification
- carried out
- oil
- ketone
- Prior art date
Links
- 238000006243 chemical reaction Methods 0.000 claims description 56
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 50
- 238000009884 interesterification Methods 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 28
- 125000005456 glyceride group Chemical group 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 24
- 150000002576 ketones Chemical class 0.000 claims description 10
- 150000003626 triacylglycerols Chemical class 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 4
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 3
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 3
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 description 29
- 239000003921 oil Substances 0.000 description 29
- 235000019198 oils Nutrition 0.000 description 29
- 239000002253 acid Substances 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 10
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- 239000003925 fat Substances 0.000 description 9
- 235000019197 fats Nutrition 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 239000002574 poison Substances 0.000 description 8
- 231100000614 poison Toxicity 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 7
- 239000003240 coconut oil Substances 0.000 description 6
- 235000019864 coconut oil Nutrition 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 230000010339 dilation Effects 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- 235000019482 Palm oil Nutrition 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000002540 palm oil Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KLTVSWGXIAYTHO-UHFFFAOYSA-N 1-Octen-3-one Chemical compound CCCCCC(=O)C=C KLTVSWGXIAYTHO-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 239000005662 Paraffin oil Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000007071 enzymatic hydrolysis Effects 0.000 description 2
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 2
- WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002600 sunflower oil Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- CJPNOLIZCWDHJK-UHFFFAOYSA-N 2-Pentadecanone Chemical compound CCCCCCCCCCCCCC(C)=O CJPNOLIZCWDHJK-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 229910000799 K alloy Inorganic materials 0.000 description 1
- 239000006001 Methyl nonyl ketone Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229910000528 Na alloy Inorganic materials 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 1
- KMPQYAYAQWNLME-UHFFFAOYSA-N Undecanal Natural products CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000021149 fatty food Nutrition 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019488 nut oil Nutrition 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/10—Ester interchange
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5764870A GB1359470A (en) | 1970-12-04 | 1970-12-04 | Interesterification process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO136457B true NO136457B (xx) | 1977-05-31 |
| NO136457C NO136457C (no) | 1977-09-07 |
Family
ID=10479685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO4469/71A NO136457C (no) | 1970-12-04 | 1971-12-03 | Fremgangsm}te for katalytisk interforestring av glycerider. |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US3809709A (xx) |
| JP (1) | JPS5249003B1 (xx) |
| AT (1) | AT319022B (xx) |
| AU (1) | AU470161B2 (xx) |
| BE (1) | BE776260A (xx) |
| CA (1) | CA928719A (xx) |
| CH (1) | CH568377A5 (xx) |
| DE (1) | DE2159614C3 (xx) |
| DK (1) | DK129787B (xx) |
| ES (1) | ES397668A1 (xx) |
| FR (1) | FR2117380A5 (xx) |
| GB (1) | GB1359470A (xx) |
| IE (1) | IE35861B1 (xx) |
| NL (1) | NL146208B (xx) |
| NO (1) | NO136457C (xx) |
| SE (1) | SE374352B (xx) |
| ZA (1) | ZA718054B (xx) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54155778U (xx) * | 1978-04-21 | 1979-10-30 | ||
| JPS5780429U (xx) * | 1980-11-05 | 1982-05-18 | ||
| JPS57162133U (xx) * | 1981-04-03 | 1982-10-12 | ||
| US5133902A (en) * | 1989-08-22 | 1992-07-28 | Viswanatha Sankaran | Transesterification of triglycerides |
| US4966876A (en) * | 1989-08-22 | 1990-10-30 | Viswanatha Sankaran | Transesterification of triglycerides |
| EP2344616A1 (en) * | 2008-10-07 | 2011-07-20 | Dow Global Technologies LLC | Nonionic surfactant blends using seed oils |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2442532A (en) * | 1945-11-13 | 1948-06-01 | Procter & Gamble | Treatment of glycerides for use in edible fats |
-
1970
- 1970-12-04 GB GB5764870A patent/GB1359470A/en not_active Expired
-
1971
- 1971-11-30 CA CA128935A patent/CA928719A/en not_active Expired
- 1971-12-01 DE DE2159614A patent/DE2159614C3/de not_active Expired
- 1971-12-01 ZA ZA718054A patent/ZA718054B/xx unknown
- 1971-12-01 AU AU36367/71A patent/AU470161B2/en not_active Expired
- 1971-12-02 IE IE1525/71A patent/IE35861B1/xx unknown
- 1971-12-02 AT AT1037371A patent/AT319022B/de not_active IP Right Cessation
- 1971-12-02 US US00204302A patent/US3809709A/en not_active Expired - Lifetime
- 1971-12-02 SE SE7115499A patent/SE374352B/xx unknown
- 1971-12-03 BE BE776260A patent/BE776260A/xx not_active IP Right Cessation
- 1971-12-03 NL NL717116621A patent/NL146208B/xx not_active IP Right Cessation
- 1971-12-03 ES ES397668A patent/ES397668A1/es not_active Expired
- 1971-12-03 CH CH1766071A patent/CH568377A5/xx not_active IP Right Cessation
- 1971-12-03 DK DK594971AA patent/DK129787B/da unknown
- 1971-12-03 FR FR7143531A patent/FR2117380A5/fr not_active Expired
- 1971-12-03 NO NO4469/71A patent/NO136457C/no unknown
- 1971-12-04 JP JP46098223A patent/JPS5249003B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BE776260A (fr) | 1972-06-05 |
| DK129787B (da) | 1974-11-18 |
| GB1359470A (en) | 1974-07-10 |
| US3809709A (en) | 1974-05-07 |
| FR2117380A5 (xx) | 1972-07-21 |
| DK129787C (xx) | 1975-04-28 |
| ZA718054B (en) | 1973-09-26 |
| AU470161B2 (en) | 1976-03-04 |
| NL7116621A (xx) | 1972-06-06 |
| CA928719A (en) | 1973-06-19 |
| AT319022B (de) | 1974-11-25 |
| SE374352B (xx) | 1975-03-03 |
| ES397668A1 (es) | 1975-03-16 |
| NL146208B (nl) | 1975-06-16 |
| IE35861L (en) | 1972-06-04 |
| NO136457C (no) | 1977-09-07 |
| AU3636771A (en) | 1973-06-07 |
| IE35861B1 (en) | 1976-06-09 |
| DE2159614C3 (de) | 1980-02-21 |
| CH568377A5 (xx) | 1975-10-31 |
| JPS5249003B1 (xx) | 1977-12-14 |
| DE2159614A1 (xx) | 1972-06-15 |
| DE2159614B2 (de) | 1979-06-21 |
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