JPH0692596B2 - Purification method of fatty acid and triglyceride - Google Patents
Purification method of fatty acid and triglycerideInfo
- Publication number
- JPH0692596B2 JPH0692596B2 JP63023281A JP2328188A JPH0692596B2 JP H0692596 B2 JPH0692596 B2 JP H0692596B2 JP 63023281 A JP63023281 A JP 63023281A JP 2328188 A JP2328188 A JP 2328188A JP H0692596 B2 JPH0692596 B2 JP H0692596B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- triglyceride
- fatty acid
- alcohol ester
- bed
- 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
- 235000014113 dietary fatty acids Nutrition 0.000 title claims description 39
- 229930195729 fatty acid Natural products 0.000 title claims description 39
- 239000000194 fatty acid Substances 0.000 title claims description 39
- 150000004665 fatty acids Chemical class 0.000 title claims description 39
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 title claims description 32
- 238000000034 method Methods 0.000 title claims description 16
- 238000000746 purification Methods 0.000 title claims description 8
- 239000007788 liquid Substances 0.000 claims description 53
- -1 alcohol ester Chemical class 0.000 claims description 34
- 239000012530 fluid Substances 0.000 claims description 14
- 239000003463 adsorbent Substances 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 11
- 239000002994 raw material Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 238000001179 sorption measurement Methods 0.000 claims description 9
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- 239000012454 non-polar solvent Substances 0.000 claims description 5
- 239000002798 polar solvent Substances 0.000 claims description 5
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 150000003626 triacylglycerols Chemical class 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 19
- 239000002156 adsorbate Substances 0.000 description 9
- 238000000926 separation method Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000004006 olive oil Substances 0.000 description 6
- 235000008390 olive oil Nutrition 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- 239000005642 Oleic acid Substances 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
- 239000003925 fat Substances 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003795 desorption Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- CNVZJPUDSLNTQU-SEYXRHQNSA-N petroselinic acid Chemical compound CCCCCCCCCCC\C=C/CCCCC(O)=O CNVZJPUDSLNTQU-SEYXRHQNSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- OXEDXHIBHVMDST-UHFFFAOYSA-N 12Z-octadecenoic acid Natural products CCCCCC=CCCCCCCCCCCC(O)=O OXEDXHIBHVMDST-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- CNVZJPUDSLNTQU-UHFFFAOYSA-N Petroselaidic acid Natural products CCCCCCCCCCCC=CCCCCC(O)=O CNVZJPUDSLNTQU-UHFFFAOYSA-N 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 description 1
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 description 1
- 235000020664 gamma-linolenic acid Nutrition 0.000 description 1
- 229960002733 gamolenic acid Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 229960002969 oleic acid Drugs 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940098695 palmitic acid Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- AQWHMKSIVLSRNY-UHFFFAOYSA-N trans-Octadec-5-ensaeure Natural products CCCCCCCCCCCCC=CCCCC(O)=O AQWHMKSIVLSRNY-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明はトリグリセリドと共に脂肪酸またはそのアルコ
ールエステルを含有する、例えば油脂の加水分解反応
液、油脂のエステル交換反応液等に含まれる、トリグリ
セリドと脂肪酸および/またはアルコールエステルとを
分解する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention contains a triglyceride and a fatty acid or an alcohol ester thereof, for example, a triglyceride and a fatty acid contained in a hydrolysis reaction liquid of fats and oils, a transesterification reaction liquid of fats and oils, and the like. And / or an alcohol ester.
[従来技術] 一般に油脂工業において、原料油脂中に不純物として含
まれる少量の脂肪酸またはそのアルコールエステルを分
離除去すること、あるいは油脂の加水分解反応やエステ
ル交換反応において反応液中に含まれるトリグリセリド
と脂肪酸またはそのアルコールエステルとを効率よく分
離することは工業上不可欠である。そのために従来は、
主に晶析法、蒸留法、あるいはアルカリを作用させる方
法等が用いられてきた。しかし、晶析法では、トリグリ
セリドと脂肪酸またはそのアルコールエステルを効率よ
く分離することは困難であり、しかも工業的規模では大
型の冷凍機を要するため経済的に不利である。一方、蒸
留法では、高温高圧を必要とするため、大きなエネルギ
ーを要し、しかも処理するトリグリセリドや脂肪酸また
はそのアルコールエステルが熱変成或いは熱分解を受け
るといった欠点を有している。又、アルカリを用いる方
法では分離効率が不十分で、しかも脂肪酸を分離後に脱
アルカリするプロセスが必要である等の欠点を有してい
る。[Prior Art] Generally, in the oil and fat industry, a small amount of a fatty acid or its alcohol ester contained as an impurity in a raw material oil and fat is separated and removed, or a triglyceride and a fatty acid contained in a reaction solution in a hydrolysis reaction or a transesterification reaction of the oil and fat. Alternatively, it is industrially essential to efficiently separate the alcohol ester. Therefore, conventionally,
A crystallization method, a distillation method, a method of allowing an alkali to act, etc. have been mainly used. However, in the crystallization method, it is difficult to efficiently separate triglyceride from fatty acid or its alcohol ester, and a large-scale refrigerator is required on an industrial scale, which is economically disadvantageous. On the other hand, the distillation method requires high temperature and high pressure and thus requires a large amount of energy, and has a drawback that the triglyceride, fatty acid or alcohol ester thereof to be processed is thermally modified or thermally decomposed. Further, the method using an alkali has drawbacks that the separation efficiency is insufficient and that a process for dealkalizing the fatty acid after separation is required.
従って、トリグリセリドと脂肪酸および/またはそのア
ルコールエステルとを低温低圧で精密にしかも経済的に
分離できる技術の開発が望まれていた。Therefore, it has been desired to develop a technique capable of accurately and economically separating triglyceride from fatty acid and / or its alcohol ester at low temperature and low pressure.
[発明の構成] 本発明者らは、脂肪酸および/またはそのアルコールエ
ステルとトリグリセリドとを精密且つ安価に分離する方
法について種々研究を重ねた結果、擬似移動床を用いれ
ば、吸着剤として疎水性の合成吸着樹脂を用い、脱離剤
として有機溶媒を用いることにより、トリグリセリドと
脂肪酸および/またはそのアルコールエステルとの連続
分離が可能であることを見出し本発明を完成するに至っ
た。[Structure of the Invention] The present inventors have conducted various studies on a method for separating a fatty acid and / or its alcohol ester from a triglyceride precisely and inexpensively. As a result, if a simulated moving bed is used, a hydrophobic adsorbent can be used. The inventors have found that continuous separation of triglyceride and fatty acid and / or its alcohol ester is possible by using a synthetic adsorption resin and an organic solvent as a desorbing agent, and have completed the present invention.
本発明で言う「脂肪酸」とは、カプリン酸、ウンデカン
酸、ラウリン酸、ミリスチン酸、アラキン酸、ステアリ
ン酸、パルミチン酸等の飽和脂肪酸、アラキドン酸、エ
イコサペンタエン酸、ミリストレイン酸、ペトロセリン
酸、エライジン酸、リノール酸、リノレン酸、γ−リノ
レン酸、ドコサヘキサエン酸、オレイン酸、パルミトレ
イン酸等の不飽和脂肪酸を全て含むものであり、「アル
コールエステル」とは、これら脂肪酸の、メチルエステ
ル、エチルエステル、プロピルエステル等の低級アルコ
ールエステルをすべて含むものである。The term "fatty acid" as used in the present invention means saturated fatty acids such as capric acid, undecanoic acid, lauric acid, myristic acid, arachidic acid, stearic acid, palmitic acid, arachidonic acid, eicosapentaenoic acid, myristoleic acid, petroselinic acid, elaidin. Acid, linoleic acid, linolenic acid, γ-linolenic acid, docosahexaenoic acid, oleic acid, those containing all unsaturated fatty acids such as palmitoleic acid, "alcohol ester", these fatty acids, methyl ester, ethyl ester, It includes all lower alcohol esters such as propyl ester.
又、本発明で言う「トリグリセリド」とは、上記の脂肪
酸をエステルとして持つトリグリセリド、ジグリセリ
ド、モノグリセリドを全て含むものである。The "triglyceride" referred to in the present invention includes all triglycerides, diglycerides and monoglycerides having the above fatty acids as esters.
即ち、本発明は、内部に吸着剤が収容されており、かつ
前端と後端とが液体通路で結合されて無端状になってい
て液体が一方向に循環している充填床に、原料液である
脂肪酸および/またはそのアルコールエステルとトリグ
リセリドの含有液および脱離液である有機溶媒を導入
し、同時に充填床からトリグリセリド精製液並びに脂肪
酸および/またはそのアルコールエステル精製液を抜出
すことからなり、充填床には、(1)原料液である脂肪
酸および/またはそのアルコールエステルとトリグリセ
リドの含有液導入口、(2)脂肪酸またはそのアルコー
ルエステル精製液抜出し口、(3)脱離液である有機溶
媒導入口および(4)トリグリセリド精製液抜出し口が
流体の流れの方向に添ってこの順序で配置され、かつこ
れらを床内の流体の流れの方向にそれらの位置を間欠的
に逐次移動させることよりなる擬似移動床を用いること
を特徴とする油脂の精製方法を提供するものである。That is, according to the present invention, the adsorbent is housed inside, and the front end and the rear end are connected by the liquid passage to form an endless shape, and the liquid is circulated in one direction. A liquid containing a fatty acid and / or an alcohol ester thereof and a triglyceride and an organic solvent that is a desorbing liquid are introduced, and at the same time, a triglyceride purified liquid and a fatty acid and / or an alcohol ester purified liquid thereof are extracted from a packed bed, In the packed bed, (1) an inlet for a liquid containing a fatty acid and / or its alcohol ester and triglyceride as a raw material liquid, (2) an outlet for a purified liquid of a fatty acid or its alcohol ester, and (3) an organic solvent as a desorbed liquid. The inlet port and the (4) triglyceride purified liquid outlet port are arranged in this order along the direction of fluid flow, and these are connected to the fluid in the bed. There is provided a method of purifying oils and fats, which comprises using a simulated moving bed consisting of moving intermittently sequentially their position in the direction of the les.
いわゆる疑似移動床、すなわち固体吸着剤が収容されて
おり、かつ前端と後端の間が流体通路で結合されてい
て、床内を流体が循環し得るようになっている充填床
に、床内の流体の流れに添って脱離液流体導入口、吸着
質流体抜出し口、原料流体導入口、非吸着質流体抜出し
口を設け、各導入口および抜出し口からそれぞれの流体
を連続的に導入または抜出し、一定時間毎に各導入口お
よび抜出し口を順次下流のそれと切り替えることによ
り、原料流体を固体吸着剤に相対的に吸着されやすい成
分(吸着質成分)および相対的に吸着されがたい成分
(非吸着成分)に分離する技術は公知であり(特公昭42
−15681号公報参照)、このような技術を利用した例と
しては、果糖の製造法(特開昭53−88335号公報参照)
やマルトースの分離法(特開昭60−67000公報参照)等
があげられる。しかしながら、擬似移動床を用いてトリ
グリセリドと脂肪酸および/またはそのアルコールエス
テルとを精密に分離する方法に関する応用例は未だ全く
報告されておらず、適用が困難とされていた。A so-called simulated moving bed, that is, a packed bed that contains a solid adsorbent and has a front end and a rear end connected by a fluid passage so that fluid can circulate in the bed, The desorbed fluid inlet, adsorbate fluid outlet, raw material fluid inlet, and non-adsorbate fluid outlet are provided along with the fluid flow of the above, and each fluid is continuously introduced from each inlet or outlet. By withdrawing and switching each inlet and outlet with the downstream one at regular time intervals, the raw material fluid is relatively easily adsorbed by the solid adsorbent (adsorbate component) and the component relatively hard to be adsorbed ( Techniques for separating into non-adsorbed components are known (Japanese Patent Publication No.
-15681), as an example of using such a technique, as a method for producing fructose (see JP-A-53-88335).
And maltose separation method (see Japanese Patent Laid-Open No. 67000/1985). However, an application example of a method for precisely separating triglyceride from fatty acid and / or its alcohol ester using a simulated moving bed has not been reported at all, and its application has been difficult.
以下、本発明についてさらに詳細に説明する。Hereinafter, the present invention will be described in more detail.
本発明において使用される疎水性の合成吸着樹脂として
はスチレンとジビニルベンゼンの共重合体を骨格とする
もので、例えばローム・アンド・ハース製アンバーライ
トXAD4、住友化学工業株式会社製デュオライトS861、三
菱化成株式会社製ダイヤイオンHP−10およびHP−20等が
挙げられるが、これらに限定されない。又、吸着樹脂の
粒径は特に限定されないが、床内の偏流を防止するため
には300〜600μmのものが望ましい。更に吸着樹脂の細
孔径についても50〜150Åのものが物質移動の点から望
ましいが、特にこれに限定されない。The hydrophobic synthetic adsorption resin used in the present invention has a skeleton of a copolymer of styrene and divinylbenzene, for example, Amberlite XAD4 manufactured by Rohm and Haas, Sumitomo Chemical Co., Ltd. Duolite S861, Examples thereof include DIAION HP-10 and HP-20 manufactured by Mitsubishi Kasei Co., Ltd., but are not limited thereto. The particle size of the adsorbent resin is not particularly limited, but is preferably 300 to 600 μm in order to prevent uneven flow in the bed. Further, the pore size of the adsorbent resin is preferably 50 to 150 Å from the viewpoint of mass transfer, but is not particularly limited thereto.
通液時の温度は高いほど高い分離能が得られるが、油脂
の安定性の面から10〜60℃が望ましい。The higher the temperature at which the solution is passed, the higher the separation ability is obtained.
本発明で脱離剤として用いる有機溶媒としては、極性溶
媒と非極性溶媒の混合溶媒が使用できる。極性溶媒とし
ては、メタノール、エタノール、プロパノール、イソプ
ロパノール、ブタノール等のアルコール類、アセトン、
メチルエチルケトン、ジエチルケトン等のケトン類、ジ
エチルエーテル、テトラヒドロフラン等のエーテル類、
並びに塩化メチレン、クロロホルム、DMF、DMSO等の物
質が、非極性溶媒としては、n−ヘキサン、n−ヘプタ
ン、n−オクタン、iso−オクタン、n−デカン等の飽
和脂肪族炭化水素、シクロヘキサン、デカリン等の環状
脂肪族炭化水素、ベンゼン、p−キシレン等の芳香族炭
化水素が挙げられるが、これらに限定されない。これら
の極性溶媒と非極性溶媒の混合比率は、トリグリセリド
並びに脂肪酸および/またはそのアルコールエステルと
吸着剤との親和力にしたがって適切に設定することが出
来る。例えば、極性溶媒としてエタノールを、非極性溶
媒としてn−ヘキサンを用いる場合、両者の混合比率を
エタノール/ヘキサン=1/9〜3/7にすれば良好な分離が
達成される。原料であるトリグリセリドと脂肪酸および
/またはそのアルコールエステルは上記の有機溶媒に溶
解させて供給することが出来るが、これは不可欠ではな
い。As the organic solvent used as the releasing agent in the present invention, a mixed solvent of a polar solvent and a nonpolar solvent can be used. As the polar solvent, alcohols such as methanol, ethanol, propanol, isopropanol, butanol, acetone,
Ketones such as methyl ethyl ketone and diethyl ketone, ethers such as diethyl ether and tetrahydrofuran,
In addition, substances such as methylene chloride, chloroform, DMF, and DMSO are used as the nonpolar solvent, saturated aliphatic hydrocarbons such as n-hexane, n-heptane, n-octane, iso-octane, and n-decane, cyclohexane, decalin. Examples thereof include cycloaliphatic hydrocarbons such as benzene, aromatic hydrocarbons such as benzene and p-xylene, but are not limited thereto. The mixing ratio of the polar solvent and the non-polar solvent can be appropriately set according to the affinity of the triglyceride and the fatty acid and / or the alcohol ester thereof and the adsorbent. For example, when ethanol is used as the polar solvent and n-hexane is used as the non-polar solvent, good separation can be achieved by setting the mixing ratio of both to ethanol / hexane = 1/9 to 3/7. The raw material triglyceride and fatty acid and / or alcohol ester thereof can be dissolved in the above-mentioned organic solvent and supplied, but this is not essential.
以下、図面に基づいて、本発明の方法をより詳細に説明
する。Hereinafter, the method of the present invention will be described in more detail with reference to the drawings.
第1図は本発明で使用する擬似移動床の一例の模式図で
ある。第1図においては、擬似移動床の主要部である充
填床の内部は16個の単位充填床に区分されているが、そ
の数は、トリグリセリドと脂肪酸および/またはそのア
ルコールエステルの組成、濃度および装置の大きさ等の
要因に従って適切に決定できる。第1図において、各単
位充填床には、疎水性の合成吸着樹脂が充填されてお
り、各単位充填床間には空間部が設けられている。各空
間部には充填床へのトリグリセリドと脂肪酸あるいはそ
のアルコールエステルの混合液の導入口および脱離液で
ある有機溶媒の導入口ならびに充填床からのトリグリセ
リド精製液抜出し口並びに脂肪酸および/またはそのア
ルコールエステル精製液抜出し口の4種類が開口してい
る(ただし、第1図ではその大部分は省略されてい
る。)。この空間部の設置は不可欠ではないが、充填床
に導入されるトリグリセリドと脂肪酸および/またはそ
のアルコールエステルの混合液および脱離液をこの空間
部に導入すると、床内を流下循環している流体中に速や
かに拡散混合させることができるので好ましい。FIG. 1 is a schematic view of an example of a simulated moving bed used in the present invention. In FIG. 1, the inside of the packed bed, which is the main part of the simulated moving bed, is divided into 16 unit packed beds, the number of which is the composition, concentration and concentration of triglyceride and fatty acid and / or its alcohol ester. It can be appropriately determined according to factors such as the size of the device. In FIG. 1, each unit packed bed is filled with a hydrophobic synthetic adsorption resin, and a space is provided between each unit packed bed. In each space, an inlet for a mixed solution of triglyceride and a fatty acid or its alcohol ester to the packed bed, an inlet for an organic solvent that is a desorbed liquid, an outlet for a purified triglyceride solution from the packed bed, and a fatty acid and / or its alcohol Four types of ester refined liquid outlets are open (however, most of them are omitted in FIG. 1). The installation of this space is not essential, but when the mixture of triglyceride and fatty acid and / or its alcohol ester and the desorbed liquid which are introduced into the packed bed are introduced into this space, the fluid flowing down in the bed is circulated. It is preferable because it can be rapidly diffused and mixed into the inside.
第1図では、空間部19にトリグリセリドと脂肪酸および
/またはそのアルコールエステルの混合液が導入され、
空間部11に脱離液として有機溶媒が導入されている。ま
た、空間部15からトリグリセリド精製液が抜出され、空
間部23から脂肪酸あるいはそのアルコールエステル精製
液が抜出されている。従って、充填床は、4個の単位充
填床109〜112からなる吸着帯域、4個の単位充填床113
〜116からなる一次精製帯域、4個の単位充填床101〜10
4からなる脱離帯域および4個の単位充填床105〜108の
4種の帯域よりなっている。各帯域の作用は、トリグリ
セリドを吸着質成分とし、脂肪酸および/またはそのア
ルコールエステルを非吸着質成分とした場合の公知の擬
似移動床のそれに等しい。In FIG. 1, a mixed solution of triglyceride and fatty acid and / or its alcohol ester is introduced into the space 19,
An organic solvent is introduced into the space 11 as a desorbed liquid. Further, the purified liquid of triglyceride is extracted from the space 15, and the purified liquid of fatty acid or its alcohol ester is extracted from the space 23. Therefore, the packed bed is an adsorption zone composed of four unit packed beds 109 to 112, and four unit packed beds 113.
~ 116 primary purification zone, 4 unit packed beds 101-10
It consists of 4 desorption zones and 4 zones of 4 unit packed beds 105-108. The action of each zone is equal to that of a known simulated moving bed in which triglyceride is the adsorbate component and fatty acid and / or its alcohol ester is the non-adsorbate component.
充填床内の液中には、トリグリセリド並びに脂肪酸およ
び/またはそのアルコールエステルの濃度分布が形成さ
れており、この濃度分布はその形状を保持しつつ下流方
向に移動する。この移動に追随するように充填床へのト
リグリセリドと脂肪酸および/またはそのアルコールエ
ステルの混合液あるいは有機溶媒の導入口並びに充填床
からのトリグリセリド精製液並びに脂肪酸および/また
はそのアルコールエステル精製液の抜出し口が順次下方
のそれに切り替えられる。切替えは4種類の開口につい
て同時に行っても良く、また各開口毎に時間的にずらし
て行ってもよい。同一の開口からの液の導入または抜出
しを継続する時間は、単位充填床の大きさ、床内を流下
する流速等により異なるが、通常、数分ないし数十分で
ある。この切替えにより、上述の4種の帯域は逐次その
充填床に占める位置を移動する。しかし、各帯域の長さ
は常にほぼ一定であり、その大きさおよび相対的位置を
保持したまま充填床を循環する。A concentration distribution of triglyceride and fatty acid and / or its alcohol ester is formed in the liquid in the packed bed, and this concentration distribution moves downstream while maintaining its shape. In order to follow this movement, a mixed liquid of triglyceride and fatty acid and / or its alcohol ester to the packed bed or an inlet for an organic solvent, and a triglyceride purified liquid and a fatty acid and / or its alcohol ester purified liquid are taken out from the packed bed. Is sequentially switched to that below. The switching may be performed for four types of openings at the same time, or may be shifted for each opening in time. The time for continuing the introduction or withdrawal of the liquid from the same opening varies depending on the size of the unit packed bed, the flow rate of the liquid flowing through the bed, etc., but is usually several minutes to several tens of minutes. By this switching, the above-mentioned four zones are successively moved to the positions occupied by the packed bed. However, the length of each zone is always almost constant and circulates through the packed bed while maintaining its size and relative position.
疎水性の吸着樹脂を吸着剤とする擬似移動床におけるト
リグリセリドと脂肪酸および/またはそのアルコールエ
ステルの分離の程度は、種々の要因により影響される
が、特に大きな要因は床内の液の流下速度、同一の開口
からの液の導入または抜出しを継続する時間である。こ
のことは、液の導入口および抜出し口の下流の開口への
切替えは、見方を替えれば導入口および抜出し口の位置
を一定にして疎水性の吸着樹脂を上流方向に移動させる
ことに等しいものであり、床内の各成分の濃度分布は、
この上流方向に移動する液との相互作用により形成され
ることからも推測される。また、この移動速度は各単位
充填床の長さ(l)を同一の開口から液の導入または抜
出しを継続する時間(T)で除したもの(l/T)に相当
する。周知のように2成分以上の成分を擬似移動床によ
り分離するには、非吸着質成分の充填床内の移動速度V1
を吸着帯域においてはV1>l/T、1次精製帯域において
はv1<l/T、脱離帯域においてはv1>l/T、2次精製帯域
においてはv1>l/Tとし、吸着質成分の充填床内の移動
速度v2を吸着帯域においてはv2<l/T、1次精製帯域に
おいてはv2<l/T、脱離帯域においてはv2>l/T、2次精
製帯域においてはv2<l/T、とすればよい。従って、液
の流下速度および同一の開口から液の導入または抜出し
を継続する時間は、これらの関係から必然的に定められ
る。一方、非吸着質成分の移動速度v1および吸着質成分
の充填床内の移動速度v2は、充填床内の液流速により決
定されるが、これらは回分式の充填床を用いて容易に実
測できるのはいうまでもない。The degree of separation of triglyceride and fatty acid and / or its alcohol ester in a simulated moving bed using a hydrophobic adsorption resin as an adsorbent is affected by various factors, and the most significant factor is the flow rate of the liquid in the bed, It is the time for continuing the introduction or withdrawal of the liquid from the same opening. This means that switching the liquid inlet and outlet to the downstream opening is equivalent to moving the hydrophobic adsorbent resin in the upstream direction with the inlet and outlet positions fixed if the viewpoint is changed. And the concentration distribution of each component in the floor is
It is inferred from the fact that it is formed by the interaction with the liquid moving in the upstream direction. This moving speed corresponds to the length (l) of each unit packed bed divided by the time (T) during which the introduction or withdrawal of the liquid is continued from the same opening (l / T). As is well known, in order to separate two or more components by a simulated moving bed, the moving speed V 1 of the non-adsorbate component in the packed bed is
Is V 1 > l / T in the adsorption zone, v 1 <l / T in the primary purification zone, v 1 > l / T in the desorption zone, and v 1 > l / T in the secondary purification zone. , the moving velocity v in 2 adsorption zone v 2 <in l / T, 1 primary purification band v 2 <l / T of the packed bed of adsorbate component in the desorption zone v 2> l / T, In the secondary purification zone, v 2 <l / T may be set. Therefore, the flow rate of the liquid and the time during which the liquid is continuously introduced or withdrawn from the same opening are inevitably determined from these relationships. On the other hand, the moving velocity v 2 of the non-adsorbates in the packed bed moving speed v 1 and adsorbate component ingredients, is determined by the liquid flow rate in the packed bed, easily using a packed bed of these batch It goes without saying that you can actually measure.
次に、実施例を用いて本発明を具体的に説明するが、本
発明はこれに限定されない。Next, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto.
実施例 内径1cm、長さ20cmのカラム16本からなる擬似移動床を
用いてオリーブオイルとオレイン酸の分離を行った。原
料液中のオリーブオイルとオレイン酸の濃度は共に20g/
であり、エタノールとヘキサンの混合溶媒(エタノー
ル/ヘキサン=2/8)に溶解した。吸着剤としては疎水
性の吸着樹脂(ローム・アンド・ハース製XAD4)を用
い、脱離液としてはエタノールとヘキサンの混合溶媒
(エタノール/ヘキサン=2/8)を使用した。原料液供
給速度は1.38ml/分、脱離液供給速度は4.27ml/分、さら
にオリーブオイル精製液の抜出しは2.83ml/分、脂肪酸
精製液の抜出しは2.83ml/分の流量で行い、原料液およ
び脱離液供給口ならびにオリーブオイル精製液およびオ
レイン酸精製液抜出し口の移動は5分毎に行った。Example Olive oil and oleic acid were separated using a simulated moving bed consisting of 16 columns having an inner diameter of 1 cm and a length of 20 cm. The concentration of both olive oil and oleic acid in the raw material liquid is 20 g /
And was dissolved in a mixed solvent of ethanol and hexane (ethanol / hexane = 2/8). A hydrophobic adsorption resin (XAD4 manufactured by Rohm and Haas) was used as the adsorbent, and a mixed solvent of ethanol and hexane (ethanol / hexane = 2/8) was used as the desorption liquid. The raw material liquid supply rate is 1.38 ml / min, the desorbed liquid supply rate is 4.27 ml / min, the olive oil refined liquid is withdrawn at 2.83 ml / min, and the fatty acid refined liquid is withdrawn at a flow rate of 2.83 ml / min. The liquid and desorbed liquid supply ports and the olive oil purified liquid and oleic acid purified liquid withdrawal ports were moved every 5 minutes.
その結果、オリーブオイル精製液中にはオレイン酸は全
く含まれず、約60分で定常状態になり、定常状態では原
料液中に含まれるオリーブオイルの97%が回収された。As a result, oleic acid was not contained at all in the purified olive oil solution, and the steady state was reached in about 60 minutes, and 97% of the olive oil contained in the raw material solution was recovered in the steady state.
[発明の効果] 本発明によれば、低温低圧の温和な条件化で、トリグリ
セリドと脂肪酸を精密に分離することができる。又、本
発明の方法は連続操作であるので、自動化を容易に行う
ことが可能であり、さらに擬似移動床の利点として吸着
剤および脱離液である有機溶媒の量を節約できることが
本発明の効果として挙げられる。[Effects of the Invention] According to the present invention, triglycerides and fatty acids can be precisely separated under mild conditions of low temperature and low pressure. In addition, since the method of the present invention is a continuous operation, it is possible to easily perform automation, and as an advantage of the simulated moving bed, it is possible to save the amounts of the adsorbent and the organic solvent that is the desorbed liquid. It can be mentioned as an effect.
第1図は、本発明の精製方法に用いる疑似移動床の模式
図である。FIG. 1 is a schematic diagram of a simulated moving bed used in the purification method of the present invention.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C07C 57/03 67/56 69/30 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location C07C 57/03 67/56 69/30
Claims (1)
が収容されており、かつ前端と後端とが液体通路で結合
されて無端状となっていて液体が一方向に循環している
充填床に、原料液である脂肪酸および/またはそのアル
コールエステルとトリグリセリドの含有液並びに脱離剤
として極性溶媒と非極性溶媒との混合溶媒である有機溶
媒を導入し、同時に充填床からトリグリセリド精製液並
びに脂肪酸および/またはそのアルコールエステル精製
液を抜出すことからなり、充填床には、(1)原料液で
ある脂肪酸および/またはそのアルコールエステルとト
リグリセリドの含有液導入口、(2)脂肪酸またはその
アルコールエステル精製液抜出し口、(3)脱離液であ
る有機溶媒導入口および(4)トリグリセリド精製液抜
出し口が流体の流れの方向に添ってこの順序で配置さ
れ、かつこれらを床内の流体の流れの方向にそれらの位
置を間欠的に逐次移動させることよりなる擬似移動床を
用いることを特徴とする脂肪酸とトリグリセリドの精製
方法。1. A hydrophobic synthetic adsorption resin as an adsorbent is housed inside, and a front end and a rear end are joined by a liquid passage to form an endless form, and a liquid circulates in one direction. A liquid containing a raw material liquid of fatty acid and / or its alcohol ester and triglyceride and an organic solvent which is a mixed solvent of a polar solvent and a non-polar solvent as a desorbing agent are introduced into the packed bed, and at the same time, a purified liquid of triglyceride from the packed bed. And a fatty acid and / or an alcohol ester purified liquid thereof are withdrawn, and in the packed bed, (1) a liquid feed port containing a fatty acid and / or its alcohol ester and triglyceride as a raw material liquid, (2) a fatty acid or its The fluid flow of the alcohol ester purified liquid outlet, (3) the organic solvent inlet which is the desorbed liquid, and (4) the triglyceride purified liquid outlet. Of fatty acids and triglycerides characterized by using a simulated moving bed which is arranged in this order along the direction of and which moves them intermittently in the direction of fluid flow in the bed. Purification method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63023281A JPH0692596B2 (en) | 1988-02-01 | 1988-02-01 | Purification method of fatty acid and triglyceride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63023281A JPH0692596B2 (en) | 1988-02-01 | 1988-02-01 | Purification method of fatty acid and triglyceride |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01197597A JPH01197597A (en) | 1989-08-09 |
JPH0692596B2 true JPH0692596B2 (en) | 1994-11-16 |
Family
ID=12106220
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63023281A Expired - Lifetime JPH0692596B2 (en) | 1988-02-01 | 1988-02-01 | Purification method of fatty acid and triglyceride |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0692596B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160193546A1 (en) * | 2013-07-31 | 2016-07-07 | Bizen Chemical Co., Ltd. | Method for separating fat-soluble substance by simulated moving bed chromatography - and device for same |
JP2015031538A (en) * | 2013-07-31 | 2015-02-16 | 備前化成株式会社 | Separation method of fat-soluble material by pseudo-moving bed chromatography using normal phase column, and device therefor |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5925600B2 (en) * | 1977-01-13 | 1984-06-19 | 三菱化学株式会社 | Fructose manufacturing method |
JPS6067000A (en) * | 1983-09-19 | 1985-04-17 | 三菱化学株式会社 | Maltose separating method |
JPS6291205A (en) * | 1985-10-16 | 1987-04-25 | Japan Organo Co Ltd | Separation of specific component in pseudo-moving bed |
-
1988
- 1988-02-01 JP JP63023281A patent/JPH0692596B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH01197597A (en) | 1989-08-09 |
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