JPS61176553A - 脂肪酸の抽出方法 - Google Patents
脂肪酸の抽出方法Info
- Publication number
- JPS61176553A JPS61176553A JP1451085A JP1451085A JPS61176553A JP S61176553 A JPS61176553 A JP S61176553A JP 1451085 A JP1451085 A JP 1451085A JP 1451085 A JP1451085 A JP 1451085A JP S61176553 A JPS61176553 A JP S61176553A
- Authority
- JP
- Japan
- Prior art keywords
- lower fatty
- fatty acid
- fatty acids
- acid
- 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.)
- Granted
Links
- 235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 49
- 229930195729 fatty acid Natural products 0.000 title claims abstract description 49
- 239000000194 fatty acid Substances 0.000 title claims abstract description 49
- 150000004665 fatty acids Chemical class 0.000 title claims abstract description 49
- 238000000034 method Methods 0.000 title claims abstract description 13
- 239000007864 aqueous solution Substances 0.000 claims abstract description 16
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 14
- 238000009835 boiling Methods 0.000 claims abstract description 12
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000012046 mixed solvent Substances 0.000 claims abstract description 10
- 150000003138 primary alcohols Chemical class 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 39
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract description 12
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract description 12
- 238000000605 extraction Methods 0.000 abstract description 11
- 239000008346 aqueous phase Substances 0.000 abstract description 9
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 abstract description 9
- 238000005192 partition Methods 0.000 abstract description 9
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract description 6
- 238000000855 fermentation Methods 0.000 abstract description 6
- 230000004151 fermentation Effects 0.000 abstract description 6
- 235000019253 formic acid Nutrition 0.000 abstract description 6
- 235000019260 propionic acid Nutrition 0.000 abstract description 6
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 4
- 239000000839 emulsion Substances 0.000 abstract description 3
- 238000000746 purification Methods 0.000 abstract description 3
- 238000000926 separation method Methods 0.000 abstract description 3
- 235000011054 acetic acid Nutrition 0.000 abstract description 2
- 238000010276 construction Methods 0.000 abstract description 2
- -1 n-hexanol Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000002904 solvent Substances 0.000 description 9
- 239000003085 diluting agent Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- VBCJJAZGEJSVTL-UHFFFAOYSA-N (Z)-18-methylnonadec-9-en-1-amine Chemical compound CC(CCCCCCCC=C/CCCCCCCCN)C VBCJJAZGEJSVTL-UHFFFAOYSA-N 0.000 description 1
- HXQPUEQDBSPXTE-UHFFFAOYSA-N Diisobutylcarbinol Chemical compound CC(C)CC(O)CC(C)C HXQPUEQDBSPXTE-UHFFFAOYSA-N 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000061 acid fraction Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 244000240602 cacao Species 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- ZAYNEGYLQMBZHR-UHFFFAOYSA-N n-butyl-5,5,7,7-tetramethyl-n-(5,5,7,7-tetramethyloct-2-enyl)oct-2-en-1-amine Chemical compound CC(C)(C)CC(C)(C)CC=CCN(CCCC)CC=CCC(C)(C)CC(C)(C)C ZAYNEGYLQMBZHR-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1451085A JPS61176553A (ja) | 1985-01-30 | 1985-01-30 | 脂肪酸の抽出方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1451085A JPS61176553A (ja) | 1985-01-30 | 1985-01-30 | 脂肪酸の抽出方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61176553A true JPS61176553A (ja) | 1986-08-08 |
| JPH0219811B2 JPH0219811B2 (enrdf_load_stackoverflow) | 1990-05-07 |
Family
ID=11863069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1451085A Granted JPS61176553A (ja) | 1985-01-30 | 1985-01-30 | 脂肪酸の抽出方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61176553A (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007522136A (ja) * | 2004-01-29 | 2007-08-09 | ズィーケム インコーポレイテッド | 有機酸の回収 |
| JP2011517445A (ja) * | 2008-03-20 | 2011-06-09 | テート アンド ライル テクノロジー リミテッド | 第三級アミド溶媒からの酸の除去 |
| WO2022239847A1 (ja) | 2021-05-14 | 2022-11-17 | リファインホールディングス株式会社 | カルボン酸の回収方法 |
| WO2024106470A1 (ja) | 2022-11-16 | 2024-05-23 | Ｓｐｉｂｅｒ株式会社 | タンパク質を含む成形体を製造する方法、及びカルボン酸を回収する方法 |
-
1985
- 1985-01-30 JP JP1451085A patent/JPS61176553A/ja active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007522136A (ja) * | 2004-01-29 | 2007-08-09 | ズィーケム インコーポレイテッド | 有機酸の回収 |
| JP2011517445A (ja) * | 2008-03-20 | 2011-06-09 | テート アンド ライル テクノロジー リミテッド | 第三級アミド溶媒からの酸の除去 |
| WO2022239847A1 (ja) | 2021-05-14 | 2022-11-17 | リファインホールディングス株式会社 | カルボン酸の回収方法 |
| WO2024106470A1 (ja) | 2022-11-16 | 2024-05-23 | Ｓｐｉｂｅｒ株式会社 | タンパク質を含む成形体を製造する方法、及びカルボン酸を回収する方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0219811B2 (enrdf_load_stackoverflow) | 1990-05-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |