SG11201405023VA - Catalyst and process for the production of acetic acid and dimetyhl ether - Google Patents

Catalyst and process for the production of acetic acid and dimetyhl ether

Info

Publication number
SG11201405023VA
SG11201405023VA SG11201405023VA SG11201405023VA SG11201405023VA SG 11201405023V A SG11201405023V A SG 11201405023VA SG 11201405023V A SG11201405023V A SG 11201405023VA SG 11201405023V A SG11201405023V A SG 11201405023VA SG 11201405023V A SG11201405023V A SG 11201405023VA
Authority
SG
Singapore
Prior art keywords
dimetyhl
ether
catalyst
production
acetic acid
Prior art date
Application number
SG11201405023VA
Other languages
English (en)
Inventor
Thomas Edward Clark
David John Law
Bruce Leo Williams
Original Assignee
Bp Chem Int Ltd
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.)
Filing date
Publication date
Application filed by Bp Chem Int Ltd filed Critical Bp Chem Int Ltd
Publication of SG11201405023VA publication Critical patent/SG11201405023VA/en

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/65—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the ferrierite type, e.g. types ZSM-21, ZSM-35 or ZSM-38, as exemplified by patent documents US4046859, US4016245 and US4046859, respectively
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
    • B01J29/7026—MFS-type, e.g. ZSM-57
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
    • B01J29/7038—MWW-type, e.g. MCM-22, ERB-1, ITQ-1, PSH-3 or SSZ-25
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B39/00—Compounds having molecular sieve and base-exchange properties, e.g. crystalline zeolites; Their preparation; After-treatment, e.g. ion-exchange or dealumination
    • C01B39/02—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof; Direct preparation thereof; Preparation thereof starting from a reaction mixture containing a crystalline zeolite of another type, or from preformed reactants; After-treatment thereof
    • C01B39/44—Ferrierite type, e.g. types ZSM-21, ZSM-35 or ZSM-38
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/095—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of organic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
    • C07C67/37—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates by reaction of ethers with carbon monoxide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
    • C07C43/04—Saturated ethers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/08—Acetic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Geology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
SG11201405023VA 2012-02-23 2013-02-22 Catalyst and process for the production of acetic acid and dimetyhl ether SG11201405023VA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12250049 2012-02-23
PCT/EP2013/053528 WO2013124404A1 (fr) 2012-02-23 2013-02-22 Catalyseur et procédé pour la production d'acide acétique et d'éther diméthylique

Publications (1)

Publication Number Publication Date
SG11201405023VA true SG11201405023VA (en) 2014-09-26

Family

ID=47747629

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201405023VA SG11201405023VA (en) 2012-02-23 2013-02-22 Catalyst and process for the production of acetic acid and dimetyhl ether

Country Status (13)

Country Link
US (1) US9302253B2 (fr)
EP (1) EP2817282A1 (fr)
JP (1) JP6082034B2 (fr)
KR (1) KR20140127263A (fr)
CN (1) CN104245650B (fr)
CA (1) CA2864632A1 (fr)
IN (1) IN2014DN06923A (fr)
MY (1) MY167587A (fr)
RU (1) RU2630675C2 (fr)
SG (1) SG11201405023VA (fr)
TW (1) TWI571457B (fr)
UA (1) UA113197C2 (fr)
WO (1) WO2013124404A1 (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101525943B1 (ko) * 2014-03-19 2015-06-09 한국화학연구원 디메틸에테르와 아세트산의 동시 제조용 불균일계 구리촉매
CN106687435B (zh) * 2014-06-20 2020-09-01 英国石油化学品有限公司 用于提纯乙酸甲酯混合物的方法
JP2017522272A (ja) * 2014-06-20 2017-08-10 ビーピー ケミカルズ リミテッドＢｐ Ｃｈｅｍｉｃａｌｓ Ｌｉｍｉｔｅｄ 酢酸およびジメチルエーテルの同時生産のためのプロセス
US9771312B2 (en) 2014-06-20 2017-09-26 Bp Chemicals Limited Process for the co-production of acetic acid and dimethyl ether
JP2017521379A (ja) * 2014-06-20 2017-08-03 ビーピー ケミカルズ リミテッドＢｐ Ｃｈｅｍｉｃａｌｓ Ｌｉｍｉｔｅｄ 酢酸およびジメチルエーテルの併産用プロセス
EP3131873A1 (fr) * 2014-06-20 2017-02-22 BP Chemicals Limited Performance catalytique améliorée dans des procédés de préparation d'acide acétique
DK3509745T3 (da) * 2016-09-09 2020-08-10 Total Res & Technology Feluy Katalysatorsammensætning omfattende modificeret krystallinsk aluminosilikat til dehydrering af alkoholer
CN111356672B (zh) 2017-08-24 2023-06-09 英国石油有限公司 甲醇脱水方法
EP3672931A4 (fr) 2017-08-24 2021-05-12 Bp P.L.C. Procédé
WO2019037769A1 (fr) * 2017-08-24 2019-02-28 Bp P.L.C. Procédé
WO2019037764A1 (fr) 2017-08-24 2019-02-28 Bp P.L.C. Procédé
EP3672929A4 (fr) 2017-08-24 2021-05-19 Bp P.L.C. Procédé
US11130118B2 (en) * 2017-11-02 2021-09-28 Tubitak Preparation of natural zeolite catalyst and the method of producing dimethyl ether from methyl alcohol using this catalyst

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4612387A (en) * 1982-01-04 1986-09-16 Air Products And Chemicals, Inc. Production of carboxylic acids and esters
US5648585A (en) * 1993-12-29 1997-07-15 Murray; Brendan Dermot Process for isomerizing linear olefins to isoolefins
US6521783B1 (en) 1998-01-29 2003-02-18 Union Carbide Chemicals & Plastics Technology Corporation Processes for preparing oxygenates
TWI465424B (zh) * 2006-03-21 2014-12-21 Bp Chem Int Ltd 製造醋酸的方法
KR100926800B1 (ko) * 2008-03-28 2009-11-12 한국화학연구원 메탄올의 탈수반응에 의한 디메틸에테르 합성용 촉매, 이의제조방법 및 디메틸에테르의 제조방법
KR100966706B1 (ko) 2008-06-18 2010-06-29 아주대학교산학협력단 메탄올로부터 디메틸에테르를 제조하는 방법
BRPI0803764A2 (pt) 2008-06-30 2010-03-09 Petroleo Brasileiro Sa sistema catalìtico e processo de sìntese direta do éter dimetìlico a partir do gás de sìntese
EP2251082A1 (fr) * 2009-05-14 2010-11-17 BP Chemicals Limited Catalyseur et procédé de carbonylation
EP2292578A1 (fr) * 2009-09-03 2011-03-09 BP Chemicals Limited Procédé de production d'acide acétique et d'éther diméthylique en présence de catalyseurs zéolites.

Also Published As

Publication number Publication date
UA113197C2 (xx) 2016-12-26
KR20140127263A (ko) 2014-11-03
RU2014138169A (ru) 2016-04-10
JP6082034B2 (ja) 2017-02-15
CN104245650A (zh) 2014-12-24
WO2013124404A1 (fr) 2013-08-29
TWI571457B (zh) 2017-02-21
CN104245650B (zh) 2019-03-12
MY167587A (en) 2018-09-20
TW201341350A (zh) 2013-10-16
IN2014DN06923A (fr) 2015-04-10
JP2015513536A (ja) 2015-05-14
US9302253B2 (en) 2016-04-05
RU2630675C2 (ru) 2017-09-12
US20150352535A1 (en) 2015-12-10
EP2817282A1 (fr) 2014-12-31
CA2864632A1 (fr) 2013-08-29

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