RU2710598C2 - Конверсия с1-3 оксигенатных соединений до с4-оксигенатных соединений, опосредованная кристаллическим микропористым материалом - Google Patents

Конверсия с1-3 оксигенатных соединений до с4-оксигенатных соединений, опосредованная кристаллическим микропористым материалом Download PDF

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RU2710598C2
RU2710598C2 RU2017101582A RU2017101582A RU2710598C2 RU 2710598 C2 RU2710598 C2 RU 2710598C2 RU 2017101582 A RU2017101582 A RU 2017101582A RU 2017101582 A RU2017101582 A RU 2017101582A RU 2710598 C2 RU2710598 C2 RU 2710598C2
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oxygenate compounds
group
compounds
oxygenate
crystalline microporous
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RU2017101582A
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RU2017101582A3 (enExample
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Сараванамуруган ШУНМУГАВЕЛЬ
ЦУБИРИ Иранцу ЗАДАБА
Эсбен ТААРНИНГ
Мартин Спангсберг ХОЛЬМ
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Хальдор Топсеэ А/С
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    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
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    • A23L27/33—Artificial sweetening agents containing sugars or derivatives
    • A23L27/34—Sugar alcohols
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
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    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/041—Mesoporous materials having base exchange properties, e.g. Si/Al-MCM-41
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    • B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
    • B01J29/405—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively containing rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead
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    • B01J29/7049—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead
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    • C01B39/06—Preparation of isomorphous zeolites characterised by measures to replace the aluminium or silicon atoms in the lattice framework by atoms of other elements, i.e. by direct or secondary synthesis
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  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
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RU2017101582A 2014-06-19 2015-06-18 Конверсия с1-3 оксигенатных соединений до с4-оксигенатных соединений, опосредованная кристаллическим микропористым материалом RU2710598C2 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14173148.9 2014-06-19
EP14173148 2014-06-19
PCT/EP2015/063774 WO2015193461A2 (en) 2014-06-19 2015-06-18 Crystalline microporous material mediated conversion of c1-3 oxygenate compounds to c4- oxygenate compounds

Publications (3)

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RU2017101582A RU2017101582A (ru) 2018-07-20
RU2017101582A3 RU2017101582A3 (enExample) 2018-12-19
RU2710598C2 true RU2710598C2 (ru) 2019-12-30

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US (1) US11034713B2 (enExample)
EP (1) EP3157939B8 (enExample)
JP (1) JP6882895B2 (enExample)
KR (1) KR20170018308A (enExample)
CN (1) CN106457230B (enExample)
BR (1) BR112016024659B8 (enExample)
CA (1) CA2949596A1 (enExample)
MX (1) MX380488B (enExample)
MY (1) MY181768A (enExample)
RU (1) RU2710598C2 (enExample)
SG (1) SG11201610525PA (enExample)
TW (1) TWI680798B (enExample)
WO (1) WO2015193461A2 (enExample)
ZA (1) ZA201606992B (enExample)

Cited By (1)

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Publication number Priority date Publication date Assignee Title
RU2741007C1 (ru) * 2020-04-16 2021-01-22 Федеральное государственное бюджетное учреждение науки "Федеральный исследовательский центр "Институт катализа им. Г.К. Борескова Сибирского отделения Российской академии наук" (ИК СО РАН, Институт катализа СО РАН) Способ получения эритрулозы из дигидроксиацетона и формальдегида

Families Citing this family (5)

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Publication number Priority date Publication date Assignee Title
EP3544947B1 (en) * 2016-11-24 2023-09-13 Topsoe A/S A method for producing glycolic acid and/or glycolate
ES2732747B2 (es) * 2018-05-25 2020-07-02 Consejo Superior Investigacion Proceso catalitico para la produccion de hidrocarburos y compuestos aromaticos a partir de compuestos oxigenados presentes en mezclas acuosas
US11292806B2 (en) * 2019-02-11 2022-04-05 Purdue Research Foundation Processes for preparing sorbose from glucose
WO2021231111A1 (en) * 2020-05-12 2021-11-18 Archer Daniels Midland Company Processes for preparing c-4 sugars and ketose sugars
CN122228219A (zh) * 2023-11-21 2026-06-16 东曹株式会社 沸石

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997043242A1 (en) * 1996-05-14 1997-11-20 Kvaerner Process Technology Limited Process for the production of 1,4-butanediol, gamma-butyrolactone and tetrahydrofuran
WO2003042200A1 (en) * 2001-11-13 2003-05-22 E.I. Du Pont De Nemours And Company Conversion of tetrahydroxybutane to tetrahydrofuran
RU2334437C2 (ru) * 2001-04-27 2008-09-27 Пепсико, Инк. Применение эритрита и d-тагатозы в диетических напитках и пищевых продуктах или в напитках и пищевых продуктах пониженной калорийности
US20090053781A1 (en) * 2004-10-14 2009-02-26 Sumitomo Chemical Company, Limited Method for Producing 2-hydroxy-4-(methylthio)butyric Acid

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ293360A (en) * 1995-05-24 1997-11-24 Kubota Kk Process for preparing crystalline microporous silicates
FR2753451B1 (fr) * 1996-09-16 1998-11-27 Roquette Freres Procede de fabrication de d-erythrose
US8227006B2 (en) 2001-04-27 2012-07-24 Pepsico, Inc. Use of erythritol and D-tagatose in diet or reduced-calorie beverages and food products
US7518026B2 (en) * 2004-10-01 2009-04-14 Exxonmobil Chemical Patents Inc. Catalyst and process for the conversion of oxygenates to olefins
CN1810753A (zh) 2006-02-28 2006-08-02 上海华谊丙烯酸有限公司 一种酸性沸石催化合成缩醛(酮)的方法
CN101024195A (zh) 2007-03-23 2007-08-29 福建师范大学 一种以hzsm-5为载体的分子筛复合氧化物催化剂的制备方法及其应用
KR102673087B1 (ko) * 2015-04-30 2024-06-10 토프쉐 에이/에스 당으로부터 메티오닌 알파-하이드록시 유사체 및 이들의 유도체의 제조를 위한 방법

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997043242A1 (en) * 1996-05-14 1997-11-20 Kvaerner Process Technology Limited Process for the production of 1,4-butanediol, gamma-butyrolactone and tetrahydrofuran
RU2334437C2 (ru) * 2001-04-27 2008-09-27 Пепсико, Инк. Применение эритрита и d-тагатозы в диетических напитках и пищевых продуктах или в напитках и пищевых продуктах пониженной калорийности
WO2003042200A1 (en) * 2001-11-13 2003-05-22 E.I. Du Pont De Nemours And Company Conversion of tetrahydroxybutane to tetrahydrofuran
US20090053781A1 (en) * 2004-10-14 2009-02-26 Sumitomo Chemical Company, Limited Method for Producing 2-hydroxy-4-(methylthio)butyric Acid

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
A. Corma, Chem. Rev. 1995, 95, 559-614 (стр. 570, таб. 6). *
Emil Dumitriu et al, Microporous and mesoporous materials, 2001, 341-359 (стр. 343, 350, 351, 355, 356, фиг. 8-9, схемы 3, 5). *
Emil Dumitriu et al, Microporous and mesoporous materials, 2001, 341-359 (стр. 343, 350, 351, 355, 356, фиг. 8-9, схемы 3, 5). СанПиН 2.3.2.2364-08 "Гигиенические требования по применению пищевых добавок" Дополнения и изменения N 1 к СанПиН 2.3.2.1293-03 (утв. постановлением Главного государственного санитарного врача РФ от 26 мая 2008 г. N 32). *
I. V. Delidovich et al, Kinetics and Catalisis, 2009, vol. 30, N 2, 297-303. *
I. V. Delidovich et al, Kinetics and Catalisis, 2009, vol. 30, N 2, 297-303. Irina V Delidovich et al, New J. Chem., 2012, 36, 2201-2204. Junhui Li et al, Catalysis Today, 2006, 116, 226-233. A. Corma, Chem. Rev. 1995, 95, 559-614 (стр. 570, таб. 6). *
Irina V Delidovich et al, New J. Chem., 2012, 36, 2201-2204. Junhui Li et al, Catalysis Today, 2006, 116, 226-233. *
Martin S. Holm et al, Green Chemistry, 2012, 14, 702-706. *
СанПиН 2.3.2.2364-08 "Гигиенические требования по применению пищевых добавок" Дополнения и изменения N 1 к СанПиН 2.3.2.1293-03 (утв. постановлением Главного государственного санитарного врача РФ от 26 мая 2008 г. N 32). *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2741007C1 (ru) * 2020-04-16 2021-01-22 Федеральное государственное бюджетное учреждение науки "Федеральный исследовательский центр "Институт катализа им. Г.К. Борескова Сибирского отделения Российской академии наук" (ИК СО РАН, Институт катализа СО РАН) Способ получения эритрулозы из дигидроксиацетона и формальдегида

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