CN103554065B - 一种使用丁二酸发酵液制备四氢呋喃的方法 - Google Patents
一种使用丁二酸发酵液制备四氢呋喃的方法 Download PDFInfo
- Publication number
- CN103554065B CN103554065B CN201310483397.XA CN201310483397A CN103554065B CN 103554065 B CN103554065 B CN 103554065B CN 201310483397 A CN201310483397 A CN 201310483397A CN 103554065 B CN103554065 B CN 103554065B
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- CN
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- Prior art keywords
- succinic acid
- thf
- tetrahydrofuran
- liquid
- esterification
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- 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.)
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 title claims abstract description 144
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 title claims abstract description 83
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 title claims abstract description 72
- 238000000034 method Methods 0.000 title claims abstract description 50
- 239000001384 succinic acid Substances 0.000 title claims abstract description 39
- 238000000855 fermentation Methods 0.000 title claims abstract description 21
- 230000004151 fermentation Effects 0.000 title claims abstract description 21
- 239000007788 liquid Substances 0.000 claims abstract description 55
- 238000005886 esterification reaction Methods 0.000 claims abstract description 42
- 230000032050 esterification Effects 0.000 claims abstract description 41
- 239000012528 membrane Substances 0.000 claims abstract description 25
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 23
- 239000000049 pigment Substances 0.000 claims abstract description 16
- 238000006243 chemical reaction Methods 0.000 claims abstract description 12
- 238000000909 electrodialysis Methods 0.000 claims abstract description 11
- 229910001415 sodium ion Inorganic materials 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 9
- 238000000926 separation method Methods 0.000 claims abstract description 9
- 239000011734 sodium Substances 0.000 claims abstract description 8
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 8
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000002500 ions Chemical class 0.000 claims abstract description 5
- 238000001914 filtration Methods 0.000 claims abstract description 3
- 230000000694 effects Effects 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 238000001704 evaporation Methods 0.000 claims description 9
- 230000008020 evaporation Effects 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 8
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 claims description 7
- 125000002091 cationic group Chemical group 0.000 claims description 6
- 230000008676 import Effects 0.000 claims description 6
- FRXSZNDVFUDTIR-UHFFFAOYSA-N 6-methoxy-1,2,3,4-tetrahydroquinoline Chemical compound N1CCCC2=CC(OC)=CC=C21 FRXSZNDVFUDTIR-UHFFFAOYSA-N 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 claims description 5
- 238000007865 diluting Methods 0.000 claims description 4
- -1 hydrogen ester Chemical class 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
- 238000010533 azeotropic distillation Methods 0.000 claims description 3
- 238000005352 clarification Methods 0.000 claims description 3
- 238000001514 detection method Methods 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000000047 product Substances 0.000 claims description 3
- 238000010992 reflux Methods 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 238000001179 sorption measurement Methods 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 238000003889 chemical engineering Methods 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 238000007599 discharging Methods 0.000 claims description 2
- 238000010494 dissociation reaction Methods 0.000 claims description 2
- 230000005593 dissociations Effects 0.000 claims description 2
- 230000005684 electric field Effects 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 238000013508 migration Methods 0.000 claims description 2
- 230000005012 migration Effects 0.000 claims description 2
- 239000002808 molecular sieve Substances 0.000 claims description 2
- 238000012856 packing Methods 0.000 claims description 2
- 230000001737 promoting effect Effects 0.000 claims description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 2
- 238000003860 storage Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000008399 tap water Substances 0.000 claims description 2
- 235000020679 tap water Nutrition 0.000 claims description 2
- 230000009286 beneficial effect Effects 0.000 abstract description 3
- 238000007670 refining Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229910017053 inorganic salt Inorganic materials 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 241000606750 Actinobacillus Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- 241000948980 Actinobacillus succinogenes Species 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 241000370738 Chlorion Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- ZBTUYCUNQBRXOR-UHFFFAOYSA-L sodium succinate hexahydrate Chemical compound O.O.O.O.O.O.[Na+].[Na+].[O-]C(=O)CCC([O-])=O ZBTUYCUNQBRXOR-UHFFFAOYSA-L 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/06—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D307/08—Preparation of tetrahydrofuran
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Description
Claims (2)
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CN201310483397.XA CN103554065B (zh) | 2013-10-16 | 2013-10-16 | 一种使用丁二酸发酵液制备四氢呋喃的方法 |
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CN201310483397.XA CN103554065B (zh) | 2013-10-16 | 2013-10-16 | 一种使用丁二酸发酵液制备四氢呋喃的方法 |
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CN103554065A CN103554065A (zh) | 2014-02-05 |
CN103554065B true CN103554065B (zh) | 2015-08-26 |
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CN110141969A (zh) * | 2019-05-27 | 2019-08-20 | 常茂生物化学工程股份有限公司 | 一种双极膜阳膜二隔室法电解分离连续制备l-酒石酸方法 |
CN112679318A (zh) * | 2020-12-28 | 2021-04-20 | 胜帮科技股份有限公司 | 一种环氧丙烷生产过程中循环溶剂的净化回收装置及方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4656297A (en) * | 1985-03-11 | 1987-04-07 | Amoco Corporation | Coproduction of butanediol and tetrahydrofuran and their subsequent separation from the reaction product mixture |
US5072009A (en) * | 1987-12-23 | 1991-12-10 | The Standard Oil Company | Vapor-phase hydrogenation of maleic anhydride to tetrahydrofuran and gamma-butyrolactone |
CN101195608A (zh) * | 2006-12-06 | 2008-06-11 | 上海焦化有限公司 | 一种分离四氢呋喃和1,4-丁二醇的方法和装置 |
CN101486637A (zh) * | 2009-02-09 | 2009-07-22 | 常茂生物化学工程股份有限公司 | 从发酵液中提取丁二酸的方法 |
CN102918011A (zh) * | 2010-04-01 | 2013-02-06 | 生物琥珀酸国际责任有限公司 | 从琥珀酸盐制备四氢呋喃、γ-丁内酯和/或丁二醇的方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3168548B2 (ja) * | 1992-11-19 | 2001-05-21 | 東ソー株式会社 | テトラヒドロフランの製造法 |
JPH0782188A (ja) * | 1993-09-14 | 1995-03-28 | Tosoh Corp | 1,4−ブタンジオールの製造方法 |
-
2013
- 2013-10-16 CN CN201310483397.XA patent/CN103554065B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4656297A (en) * | 1985-03-11 | 1987-04-07 | Amoco Corporation | Coproduction of butanediol and tetrahydrofuran and their subsequent separation from the reaction product mixture |
US5072009A (en) * | 1987-12-23 | 1991-12-10 | The Standard Oil Company | Vapor-phase hydrogenation of maleic anhydride to tetrahydrofuran and gamma-butyrolactone |
CN101195608A (zh) * | 2006-12-06 | 2008-06-11 | 上海焦化有限公司 | 一种分离四氢呋喃和1,4-丁二醇的方法和装置 |
CN101486637A (zh) * | 2009-02-09 | 2009-07-22 | 常茂生物化学工程股份有限公司 | 从发酵液中提取丁二酸的方法 |
CN102918011A (zh) * | 2010-04-01 | 2013-02-06 | 生物琥珀酸国际责任有限公司 | 从琥珀酸盐制备四氢呋喃、γ-丁内酯和/或丁二醇的方法 |
Non-Patent Citations (2)
Title |
---|
付丽丽,等.双极膜电渗析提取琥珀酸.《水处理技术》.2013,第39卷(第3期),摘要,第35-37页. * |
李青山,等.五效蒸发器的工作原理.《腈纶生产工学》.中国纺织出版社,2000,(第1版),第133-134页第二节. * |
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CN103554065A (zh) | 2014-02-05 |
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Effective date of registration: 20161206 Address after: 072150 Hebei city of Baoding province Mancheng District in Pang village Jia Zhuang Xiang Patentee after: BLRH BIOTECH Co. Address before: 214407 Jiangsu city of Wuxi province Jiangyin Xu Xiake Zhen Huang Tang Industrial Park Fu Industry Road No. 7 Patentee before: JIANGYIN AORUINUO BIOTECHNOLOGY Co.,Ltd. |
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Effective date of registration: 20220705 Address after: 443000 room 1018, No. 57-5, development avenue, Yichang District, China (Hubei) free trade zone, Yichang City, Hubei Province Patentee after: Hubei Guoxin Juzhi New Material Technology Co.,Ltd. Address before: 201512 Shanghai city Jinshan District Qiushi Road No. 688 Patentee before: Shanghai Mayers biochemical technology center |
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Effective date of registration: 20230110 Address after: Room 518-20, No. 28, Songyang Yili, Fengxiang Street, Xiang'an District, Xiamen, Fujian, 361102 Patentee after: Shien (Xiamen) Biotechnology Co.,Ltd. Address before: 443000 room 1018, No. 57-5, development avenue, Yichang District, China (Hubei) free trade zone, Yichang City, Hubei Province Patentee before: Hubei Guoxin Juzhi New Material Technology Co.,Ltd. |
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