MX369164B - Procedimiento para producir ácido acético. - Google Patents

Procedimiento para producir ácido acético.

Info

Publication number
MX369164B
MX369164B MX2017015453A MX2017015453A MX369164B MX 369164 B MX369164 B MX 369164B MX 2017015453 A MX2017015453 A MX 2017015453A MX 2017015453 A MX2017015453 A MX 2017015453A MX 369164 B MX369164 B MX 369164B
Authority
MX
Mexico
Prior art keywords
prc
methyl iodide
mixture
acetic acid
stream
Prior art date
Application number
MX2017015453A
Other languages
English (en)
Other versions
MX2017015453A (es
Inventor
Masahiko Shimizu
Hiroyuki Miura
Mizutani Yoshihisa
Original Assignee
Daicel 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.)
Filing date
Publication date
Application filed by Daicel Corp filed Critical Daicel Corp
Publication of MX2017015453A publication Critical patent/MX2017015453A/es
Publication of MX369164B publication Critical patent/MX369164B/es

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/06—Flash distillation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/14—Fractional distillation or use of a fractionation or rectification column
    • B01D3/143—Fractional distillation or use of a fractionation or rectification column by two or more of a fractionation, separation or rectification step
    • B01D3/148—Fractional distillation or use of a fractionation or rectification column by two or more of a fractionation, separation or rectification step in combination with at least one evaporator
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/34—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
    • B01D3/40—Extractive distillation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
    • B01D5/0057—Condensation of vapours; Recovering volatile solvents by condensation in combination with other processes
    • B01D5/006—Condensation of vapours; Recovering volatile solvents by condensation in combination with other processes with evaporation or distillation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/38—Separation; Purification; Stabilisation; Use of additives
    • C07C17/383—Separation; Purification; Stabilisation; Use of additives by distillation
    • C07C17/386—Separation; Purification; Stabilisation; Use of additives by distillation with auxiliary compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C19/00—Acyclic saturated compounds containing halogen atoms
    • C07C19/07—Acyclic saturated compounds containing halogen atoms containing iodine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B61/00—Other general methods

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Se proporciona un procedimiento para producir ácido acético mientras se separan de modo eficaz los compuestos reductores de permanganato (PRC) y el yoduro de metilo; los PRC se separan o remueven de una composición mezclada (3A) que contiene los PRC y yoduro de metilo al destilar la composición mezclada en un paso de destilación (5) para formar una corriente de producto evaporado (5A), una corriente de extracción lateral (5B), y una corriente inferior (5C); en una columna de destilación del paso de destilación (5), se agrega un extractante (por ejemplo, agua) que extrae los PRC preferentemente al yoduro de metilo a una zona de concentración en la que se concentran los PRC y el yoduro de metilo, y se separa una mezcla de extracción que cae desde la zona de concentración como la corriente de extracción lateral (5B).
MX2017015453A 2015-06-01 2016-05-27 Procedimiento para producir ácido acético. MX369164B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2015111750 2015-06-01
PCT/JP2016/065822 WO2016194850A1 (ja) 2015-06-01 2016-05-27 酢酸の製造方法

Publications (2)

Publication Number Publication Date
MX2017015453A MX2017015453A (es) 2018-03-08
MX369164B true MX369164B (es) 2019-10-30

Family

ID=57442102

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017015453A MX369164B (es) 2015-06-01 2016-05-27 Procedimiento para producir ácido acético.

Country Status (14)

Country Link
US (1) US10562836B2 (es)
EP (1) EP3257833B1 (es)
JP (1) JP6359769B2 (es)
KR (1) KR102675319B1 (es)
CN (1) CN107709279B (es)
AR (1) AR106823A1 (es)
BR (1) BR112017020974B1 (es)
ES (1) ES2757562T3 (es)
MX (1) MX369164B (es)
MY (1) MY179732A (es)
SA (1) SA517390402B1 (es)
SG (1) SG11201707009TA (es)
TW (1) TWI659014B (es)
WO (1) WO2016194850A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10265639B2 (en) 2016-07-07 2019-04-23 Daicel Corporation Process for producing acetic acid
CN109415291B (zh) * 2016-07-07 2022-01-04 株式会社大赛璐 乙酸制造工艺
US10428004B2 (en) 2017-01-18 2019-10-01 Daicel Corporation Method for producing acetic acid
CN110049963B (zh) * 2017-01-18 2022-02-18 株式会社大赛璐 乙酸的制备方法
US10207977B2 (en) 2017-01-18 2019-02-19 Daicel Corporation Method for producing acetic acid
WO2018135016A1 (ja) * 2017-01-18 2018-07-26 株式会社ダイセル 酢酸の製造方法
CN110191874A (zh) * 2017-03-28 2019-08-30 株式会社大赛璐 乙酸的制备方法
US10308581B2 (en) 2017-03-28 2019-06-04 Daicel Corporation Method for producing acetic acid
WO2021202270A1 (en) 2020-04-01 2021-10-07 Celanese International Corporation Processes for removing and/or reducing permanganate reducing compounds and alkyl iodides
TW202212311A (zh) * 2020-06-03 2022-04-01 美商瑟蘭斯國際股份有限公司 製程流之縮醛移除
JP2023528451A (ja) * 2020-06-03 2023-07-04 セラニーズ・インターナショナル・コーポレーション 酢酸の製造及び精製
MX2022015384A (es) 2020-06-03 2023-01-16 Celanese Int Corp Proceso para la produccion de acido acetico mediante la eliminacion de compuestos reductores de permanganato.

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4241219A (en) * 1979-07-30 1980-12-23 Halcon Research And Development Corp. Treatment of carbonylation effluent
JP3244385B2 (ja) 1994-06-15 2002-01-07 ダイセル化学工業株式会社 高純度酢酸の製造方法
US5625095A (en) * 1994-06-15 1997-04-29 Daicel Chemical Industries, Ltd. Process for producing high purity acetic acid
JP2001096102A (ja) * 1999-09-29 2001-04-10 Nippon Shokubai Co Ltd 精製塔の液抜き出し用トレイ、精製塔および精製方法
CN1411432A (zh) * 1999-12-22 2003-04-16 伊斯曼化学公司 增强的从羰基化工艺中除去丙酮的方法
WO2012046593A1 (ja) * 2010-10-06 2012-04-12 ダイセル化学工業株式会社 酢酸の製造方法
US8859810B2 (en) 2012-08-21 2014-10-14 Celanese International Corporation Process for recovering permanganate reducing compounds from an acetic acid production process
US9512056B2 (en) * 2015-02-04 2016-12-06 Celanese International Corporation Process to control HI concentration in residuum stream

Also Published As

Publication number Publication date
MY179732A (en) 2020-11-12
CN107709279B (zh) 2021-10-08
KR20180013888A (ko) 2018-02-07
AR106823A1 (es) 2018-02-21
WO2016194850A1 (ja) 2016-12-08
JP6359769B2 (ja) 2018-07-18
BR112017020974A2 (pt) 2018-07-10
JPWO2016194850A1 (ja) 2017-12-14
SA517390402B1 (ar) 2021-03-30
KR102675319B1 (ko) 2024-06-17
US20180118651A1 (en) 2018-05-03
TW201708176A (zh) 2017-03-01
EP3257833B1 (en) 2019-10-16
ES2757562T3 (es) 2020-04-29
MX2017015453A (es) 2018-03-08
EP3257833A1 (en) 2017-12-20
EP3257833A4 (en) 2018-03-28
SG11201707009TA (en) 2017-09-28
US10562836B2 (en) 2020-02-18
BR112017020974B1 (pt) 2020-11-24
CN107709279A (zh) 2018-02-16
TWI659014B (zh) 2019-05-11

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