UA113197C2 - Спосіб одержання оцтової кислоти і диметилового ефіру - Google Patents

Спосіб одержання оцтової кислоти і диметилового ефіру

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Publication number
UA113197C2
UA113197C2 UAA201410281A UAA201410281A UA113197C2 UA 113197 C2 UA113197 C2 UA 113197C2 UA A201410281 A UAA201410281 A UA A201410281A UA A201410281 A UAA201410281 A UA A201410281A UA 113197 C2 UA113197 C2 UA 113197C2
Authority
UA
Ukraine
Prior art keywords
acetic acid
dimethyl ether
preparation
methanol
mixture
Prior art date
Application number
UAA201410281A
Other languages
English (en)
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 filed Critical
Publication of UA113197C2 publication Critical patent/UA113197C2/uk

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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)

Abstract

Винахід стосується способу спільного одержання оцтової кислоти і диметилового ефіру з суміші метанолу і метилацетату при температурі, що дорівнює від 200 до 260 °С із каталітичною композицією, що включає цеоліт, що містить 2-мірну канальну систему, яка містить щонайменше один канал, утворений 10-членними кільцями, і має молярне відношення діоксид кремнію:оксид алюмінію, становить щонайменше 22:1.
UAA201410281A 2012-02-23 2013-02-22 Спосіб одержання оцтової кислоти і диметилового ефіру UA113197C2 (xx)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12250049 2012-02-23
PCT/EP2013/053528 WO2013124404A1 (en) 2012-02-23 2013-02-22 Catalyst and process for the production of acetic acid and dimetyhl ether

Publications (1)

Publication Number Publication Date
UA113197C2 true UA113197C2 (xx) 2016-12-26

Family

ID=47747629

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA201410281A UA113197C2 (xx) 2012-02-23 2013-02-22 Спосіб одержання оцтової кислоти і диметилового ефіру

Country Status (13)

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

Families Citing this family (15)

* 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
EP3131873A1 (en) 2014-06-20 2017-02-22 BP Chemicals Limited Improved catalytic performance in processes for preparing acetic acid
WO2015193188A1 (en) * 2014-06-20 2015-12-23 Bp Chemicals Limited Process for the co-production of acetic acid and dimethyl ether
CN106687436A (zh) * 2014-06-20 2017-05-17 英国石油化学品有限公司 联合生产乙酸和二甲醚的方法
SG11201609785YA (en) * 2014-06-20 2017-01-27 Bp Chem Int Ltd Process for purifying methyl acetate mixtures
EP3131867A1 (en) * 2014-06-20 2017-02-22 BP Chemicals Limited Process for the co-production of acetic acid and dimethyl ether
US10851028B2 (en) * 2016-09-09 2020-12-01 Total Research & Technology Feluy Process for dehydration of mono-alcohol(s) using a modified crystalline aluminosilicate
EP3672931A4 (en) 2017-08-24 2021-05-12 Bp P.L.C. PROCESS
CN111511709B (zh) * 2017-08-24 2023-05-30 英国石油有限公司 甲醇脱水方法
WO2019037769A1 (en) * 2017-08-24 2019-02-28 Bp P.L.C. PROCESS
WO2019037764A1 (en) 2017-08-24 2019-02-28 Bp P.L.C. PROCESS
CN111356672B (zh) 2017-08-24 2023-06-09 英国石油有限公司 甲醇脱水方法
WO2019087139A2 (en) * 2017-11-02 2019-05-09 Tubitak The preparation of natural zeolite catalyst and the method of producing dimethyl ether from methyl alcohol using this catalyst
CN113677655B (zh) 2019-02-22 2024-03-19 英国石油有限公司 一种二甲醚的生产方法
WO2020168539A1 (en) 2019-02-22 2020-08-27 Bp P.L.C. Process

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 (en) * 2009-05-14 2010-11-17 BP Chemicals Limited Carbonylation catalyst and process
EP2292578A1 (en) * 2009-09-03 2011-03-09 BP Chemicals Limited Process for producing acetic acid and dimethyl ether using a zeolite catalyst

Also Published As

Publication number Publication date
CN104245650A (zh) 2014-12-24
JP2015513536A (ja) 2015-05-14
US20150352535A1 (en) 2015-12-10
RU2630675C2 (ru) 2017-09-12
CN104245650B (zh) 2019-03-12
KR20140127263A (ko) 2014-11-03
TWI571457B (zh) 2017-02-21
JP6082034B2 (ja) 2017-02-15
CA2864632A1 (en) 2013-08-29
SG11201405023VA (en) 2014-09-26
TW201341350A (zh) 2013-10-16
EP2817282A1 (en) 2014-12-31
WO2013124404A1 (en) 2013-08-29
MY167587A (en) 2018-09-20
RU2014138169A (ru) 2016-04-10
IN2014DN06923A (uk) 2015-04-10
US9302253B2 (en) 2016-04-05

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