JPS63230068A - 醗酵ガスよりエステル類を回収する方法 - Google Patents

醗酵ガスよりエステル類を回収する方法

Info

Publication number: JPS63230068A
Authority: JP; Japan
Prior art keywords: esters; zeolite; recovery; adsorption; fermentation process
Prior art date: 1987-03-20
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

Application number

JP62064286A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0329384B2 (cs

Inventor

Akio Furuta

昭男古田

Sakae Inagaki

稲垣　栄

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

JGC Corp

Original Assignee

JGC Corp

Priority date (The priority date 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 date listed.)

1987-03-20

Filing date

1987-03-20

Publication date

1988-09-26

1987-03-20 Application filed by JGC Corp filed Critical JGC Corp

1987-03-20 Priority to JP62064286A priority Critical patent/JPS63230068A/ja

1988-09-26 Publication of JPS63230068A publication Critical patent/JPS63230068A/ja

1991-04-24 Publication of JPH0329384B2 publication Critical patent/JPH0329384B2/ja

Status Granted legal-status Critical Current

Links

150000002148 esters Chemical class 0.000 title claims abstract description 27
238000000855 fermentation Methods 0.000 title claims abstract description 17
230000004151 fermentation Effects 0.000 title claims abstract description 17
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 38
229910021536 Zeolite Inorganic materials 0.000 claims abstract description 26
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 26
239000010457 zeolite Substances 0.000 claims abstract description 26
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 24
239000000377 silicon dioxide Substances 0.000 claims abstract description 15
-1 organosilane compound Chemical class 0.000 claims abstract description 6
238000000034 method Methods 0.000 claims description 17
229910000077 silane Inorganic materials 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
239000003463 adsorbent Substances 0.000 abstract description 8
229910052681 coesite Inorganic materials 0.000 abstract description 7
229910052906 cristobalite Inorganic materials 0.000 abstract description 7
229910052682 stishovite Inorganic materials 0.000 abstract description 7
229910052905 tridymite Inorganic materials 0.000 abstract description 7
125000003118 aryl group Chemical group 0.000 abstract description 6
235000012239 silicon dioxide Nutrition 0.000 abstract description 4
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
229910052593 corundum Inorganic materials 0.000 abstract description 2
239000003960 organic solvent Substances 0.000 abstract description 2
229910001845 yogo sapphire Inorganic materials 0.000 abstract description 2
230000001476 alcoholic effect Effects 0.000 abstract 2
238000003795 desorption Methods 0.000 abstract 1
238000011084 recovery Methods 0.000 description 20
238000001179 sorption measurement Methods 0.000 description 19
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 15
239000007789 gas Substances 0.000 description 12
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 6
239000007788 liquid Substances 0.000 description 6
239000000706 filtrate Substances 0.000 description 5
239000001760 fusel oil Substances 0.000 description 5
RGXWDWUGBIJHDO-UHFFFAOYSA-N ethyl decanoate Chemical compound CCCCCCCCCC(=O)OCC RGXWDWUGBIJHDO-UHFFFAOYSA-N 0.000 description 4
SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000001816 cooling Methods 0.000 description 3
239000000796 flavoring agent Substances 0.000 description 3
235000013355 food flavoring agent Nutrition 0.000 description 3
229940117955 isoamyl acetate Drugs 0.000 description 3
PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 3
229910052680 mordenite Inorganic materials 0.000 description 3
WJTCHBVEUFDSIK-NWDGAFQWSA-N (2r,5s)-1-benzyl-2,5-dimethylpiperazine Chemical compound C[C@@H]1CN[C@@H](C)CN1CC1=CC=CC=C1 WJTCHBVEUFDSIK-NWDGAFQWSA-N 0.000 description 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
150000001733 carboxylic acid esters Chemical class 0.000 description 2
238000001914 filtration Methods 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000002808 molecular sieve Substances 0.000 description 2
YYZUSRORWSJGET-UHFFFAOYSA-N octanoic acid ethyl ester Natural products CCCCCCCC(=O)OCC YYZUSRORWSJGET-UHFFFAOYSA-N 0.000 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 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
229920000049 Carbon (fiber) Polymers 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
235000013334 alcoholic beverage Nutrition 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
235000019568 aromas Nutrition 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000010276 construction Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229910001657 ferrierite group Inorganic materials 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
229940035429 isobutyl alcohol Drugs 0.000 description 1
FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
239000000203 mixture Substances 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
FPLYNRPOIZEADP-UHFFFAOYSA-N octylsilane Chemical group CCCCCCCC[SiH3] FPLYNRPOIZEADP-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1

Landscapes

Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP62064286A 1987-03-20 1987-03-20 醗酵ガスよりエステル類を回収する方法 Granted JPS63230068A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP62064286A JPS63230068A (ja)	1987-03-20	1987-03-20	醗酵ガスよりエステル類を回収する方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP62064286A JPS63230068A (ja)	1987-03-20	1987-03-20	醗酵ガスよりエステル類を回収する方法

Publications (2)

Publication Number	Publication Date
JPS63230068A true JPS63230068A (ja)	1988-09-26
JPH0329384B2 JPH0329384B2 (cs)	1991-04-24

Family

ID=13253838

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62064286A Granted JPS63230068A (ja)	1987-03-20	1987-03-20	醗酵ガスよりエステル類を回収する方法

Country Status (1)

Country	Link
JP (1)	JPS63230068A (cs)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN102742815A (zh) *	2011-04-19	2012-10-24	丰益(上海)生物技术研发中心有限公司	一种获得奶酪风味物质的新方法

1987
- 1987-03-20 JP JP62064286A patent/JPS63230068A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN102742815A (zh) *	2011-04-19	2012-10-24	丰益(上海)生物技术研发中心有限公司	一种获得奶酪风味物质的新方法

Also Published As

Publication number	Publication date
JPH0329384B2 (cs)	1991-04-24

Publication	Publication Date	Title
US4465875A (en)	1984-08-14	Process for dehydrating ethanol
JPH0761964B2 (ja)	1995-07-05	１，１，１，２―テトラフルオロエタンの精製方法
JP7317969B2 (ja)	2023-07-31	改善された風味を有する非アルコール性発酵ビール
JP4800955B2 (ja)	2011-10-26	ターシャリーブチルアルコールの精製
HUP0104714A2 (hu)	2002-03-28	Eljárás szerves folyadékok víztelenítésére
JPH0329385B2 (cs)	1991-04-24
JPH0329386B2 (cs)	1991-04-24
DE4339500A1 (de)	1995-05-24	Simultane Sorption von Wasser und organischen Verbindungen
JPH0329384B2 (cs)	1991-04-24
CN1073547C (zh)	2001-10-24	从酯产物中除去溶解的金属催化剂的方法
JPH0335910B2 (cs)	1991-05-29
EP0278792A2 (en)	1988-08-17	Method for simultaneous removal of aromatics and wax from lube distillate by an adsorption process
JPH05201893A (ja)	1993-08-10	１，１，１，２−テトラフルオロエタンの精製法
JPH0899919A (ja)	1996-04-16	ジフルオロメタンの精製法
JPH0462714B2 (cs)	1992-10-07
JPS63304973A (ja)	1988-12-13	醗酵ガスよりエステル類を回収する方法
JPH09227550A (ja)	1997-09-02	エチレンカーボネートの精製方法
JPH0560825B2 (cs)	1993-09-03
US5942458A (en)	1999-08-24	Regeneration of spent As-poisoned lead catalysts
US4424120A (en)	1984-01-03	Process for removal of alkyl lead impurities from liquid hydrocarbons
RU2196127C1 (ru)	2003-01-10	Способ очистки этилового спирта
CN109456162B (zh)	2021-11-26	一种色谱纯4-甲基-2-戊酮的纯化方法
CA1096779A (en)	1981-03-03	Process for the separation of unsaturated compounds from liquid hydrocarbon mixtures
JPS63290845A (ja)	1988-11-28	高度不飽和脂肪酸エステルの濃縮分離方法
CA1221985A (en)	1987-05-19	Process for dehydrating ethanol

JPS63230068A - 醗酵ガスよりエステル類を回収する方法 - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=13253838

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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