RU96109707A - METHOD FOR PRODUCING ACETIC ACID BY CARBONILING - Google Patents

METHOD FOR PRODUCING ACETIC ACID BY CARBONILING

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Publication number
RU96109707A
RU96109707A RU96109707/04A RU96109707A RU96109707A RU 96109707 A RU96109707 A RU 96109707A RU 96109707/04 A RU96109707/04 A RU 96109707/04A RU 96109707 A RU96109707 A RU 96109707A RU 96109707 A RU96109707 A RU 96109707A
Authority
RU
Russia
Prior art keywords
concentration
reaction mixture
liquid reaction
during
interaction
Prior art date
Application number
RU96109707/04A
Other languages
Russian (ru)
Other versions
RU2160248C2 (en
Inventor
Джеймс Бейкер Майкл
Шермэн Гарлэнд Карл
Фрэнсис Гайлс Мартин
Джеймс Маскетт Майкл
Рафелетос Георгиос
Джеймс СМИТ Стивен
Гленн Санли Джон
Джон Уатт Роберт
Лео Вилльямс Брюс
Original Assignee
Бп Кемикэлз Лимитед
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
Priority claimed from GBGB9512606.6A external-priority patent/GB9512606D0/en
Priority claimed from GBGB9514745.0A external-priority patent/GB9514745D0/en
Priority claimed from GBGB9520441.8A external-priority patent/GB9520441D0/en
Priority claimed from GBGB9524037.0A external-priority patent/GB9524037D0/en
Application filed by Бп Кемикэлз Лимитед filed Critical Бп Кемикэлз Лимитед
Publication of RU96109707A publication Critical patent/RU96109707A/en
Application granted granted Critical
Publication of RU2160248C2 publication Critical patent/RU2160248C2/en

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Claims (10)

1. Способ получения уксусной кислоты, включающий (1) непрерывную подачу метанола и/или его реакционноспособного производного и моноокиси углерода в реактор для карбонилирования, который содержит жидкую реакционную смесь, включающую иридиевый катализатор карбонилирования, метилиодидный сокатализатор, воду в ограниченной концентрации, уксусную кислоту, метилацетат и по меньшей мере один промотор; (2) введение метанола и/или его реакционноспособного производного в контакт с моноокисью углерода в жидкой реакционной смеси с получением уксусной кислоты и (3) выделение уксусной кислоты из жидкой реакционной смеси, отличающийся тем, что в ходе проведения взаимодействия в жидкой реакционной смеси постоянно поддерживают (а) концентрацию воды не свыше 6,5 вес.%, (б) концентрацию метилацетата в пределах 1-35 вес.% и (в) концентрацию метилиодида в пределах 4-20 вес.%.1. A method for producing acetic acid, comprising (1) continuously supplying methanol and / or a reactive derivative thereof and carbon monoxide to a carbonylation reactor, which contains a liquid reaction mixture including an iridium carbonylation catalyst, methyl iodide cocatalyst, water in a limited concentration, acetic acid, methyl acetate and at least one promoter; (2) introducing methanol and / or its reactive derivative into contact with carbon monoxide in a liquid reaction mixture to obtain acetic acid; and (3) separating acetic acid from the liquid reaction mixture, characterized in that during the course of the reaction, the liquid reaction mixture is constantly maintained (a) the concentration of water is not more than 6.5 wt.%, (b) the concentration of methyl acetate in the range of 1-35 wt.% and (c) the concentration of methyl iodide in the range of 4-20 wt.%. 2. Способ по п. 1, в котором в ходе проведения взаимодействия в жидкой реакционной смеси постоянно поддерживают концентрацию воды не более 6 вес.%. 2. The method according to p. 1, in which during the interaction in the liquid reaction mixture constantly maintain a water concentration of not more than 6 wt.%. 3. Способ по п. 1 или 2, в котором в ходе проведения взаимодействия в жидкой реакционной смеси постоянно поддерживают концентрацию воды по меньшей мере 0,1 вес.%. 3. The method according to p. 1 or 2, in which during the interaction in the liquid reaction mixture constantly maintain a water concentration of at least 0.1 wt.%. 4. Способ по п. 3, в котором в ходе проведения взаимодействия в жидкой реакционной смеси постоянно поддерживают концентрацию воды по меньшей мере 1 вес.%. 4. The method according to p. 3, in which during the interaction in the liquid reaction mixture constantly maintain a water concentration of at least 1 wt.%. 5. Способ по любому из предыдущих пунктов, в котором в ходе проведения взаимодействия концентрацию метилацетата в жидкой реакционной смеси постоянно поддерживают в пределах 1-30 вес.%. 5. The method according to any one of the preceding paragraphs, in which during the interaction the concentration of methyl acetate in the liquid reaction mixture is constantly maintained within the range of 1-30 wt.%. 6. Способ по п. 5, в котором в ходе проведения взаимодействия концентрацию метилацетата в жидкой реакционной смеси постоянно поддерживают в пределах 5-25 вес.%. 6. The method according to p. 5, in which during the interaction the concentration of methyl acetate in the liquid reaction mixture is constantly maintained in the range of 5-25 wt.%. 7. Способ по любому из предыдущих пунктов, в котором в ходе проведения взаимодействия концентрацию метилиодида в жидкой реакционной смеси постоянно поддерживают в пределах 5-16 вес.%. 7. The method according to any one of the preceding paragraphs, in which during the interaction the concentration of methyl iodide in the liquid reaction mixture is constantly maintained in the range of 5-16 wt.%. 8. Способ по любому из предыдущих пунктов, в котором по меньшей мере один промотор выбирают из группы, состоящей из рутения, осмия, рения, кадмия, ртути, цинка, галлия, индия и вольфрама, предпочтительно из группы, состоящей из рутения и осмия. 8. The method according to any one of the preceding paragraphs, in which at least one promoter is selected from the group consisting of ruthenium, osmium, rhenium, cadmium, mercury, zinc, gallium, indium and tungsten, preferably from the group consisting of ruthenium and osmium. 9. Способ по п. 8, в котором молярное соотношение промотор: иридий составляет (0,5-15):1. 9. The method according to p. 8, in which the molar ratio of promoter: iridium is (0.5-15): 1. 10. Способ по п. 1, в котором в ходе проведения взаимодействия в жидкой реакционной смеси постоянно поддерживают содержание приблизительно 5 вес. % воды, примерно 7 вес. % метилиодида, около 15% метилацетата, концентрацию иридиевого катализатора в пределах 400-3000 частей/млн и концентрацию рутениевого промотора в пределах 400-4000 частей/млн. 10. The method according to p. 1, in which during the interaction in the liquid reaction mixture constantly maintain a content of approximately 5 weight. % water, about 7 weight. % methyl iodide, about 15% methyl acetate, the concentration of the iridium catalyst in the range of 400-3000 ppm and the concentration of the ruthenium promoter in the range of 400-4000 ppm.
RU96109707/04A 1995-06-21 1996-05-13 Method of preparing acetic acid by carbonylation RU2160248C2 (en)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
GB9512606.6 1995-06-21
GBGB9512606.6A GB9512606D0 (en) 1995-06-21 1995-06-21 Process
GB9514745.0 1995-07-19
GBGB9514745.0A GB9514745D0 (en) 1995-07-19 1995-07-19 Process
GB9520441.8 1995-10-06
GBGB9520441.8A GB9520441D0 (en) 1995-10-06 1995-10-06 Process
GB9524037.0 1995-11-23
GBGB9524037.0A GB9524037D0 (en) 1995-11-23 1995-11-23 Process

Publications (2)

Publication Number Publication Date
RU96109707A true RU96109707A (en) 1998-08-20
RU2160248C2 RU2160248C2 (en) 2000-12-10

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RU96109707/04A RU2160248C2 (en) 1995-06-21 1996-05-13 Method of preparing acetic acid by carbonylation
RU96109188/04A RU2167850C2 (en) 1995-06-21 1996-05-13 Method of carbonylation of alkyl-aliphatic alcohols and/or reactive derivatives thereof

Family Applications After (1)

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RU96109188/04A RU2167850C2 (en) 1995-06-21 1996-05-13 Method of carbonylation of alkyl-aliphatic alcohols and/or reactive derivatives thereof

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US (1) US5696284A (en)
EP (2) EP0749948B1 (en)
JP (2) JP3884504B2 (en)
KR (2) KR970001296A (en)
CN (2) CN1068576C (en)
AR (2) AR002559A1 (en)
AT (2) ATE194825T1 (en)
CA (2) CA2175028C (en)
DE (2) DE69609381T2 (en)
MX (2) MX9602083A (en)
MY (2) MY113453A (en)
NO (2) NO961723L (en)
NZ (2) NZ286473A (en)
RU (2) RU2160248C2 (en)
TW (2) TW396150B (en)
UA (2) UA50713C2 (en)

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FR2725443B1 (en) * 1994-10-05 1996-12-20 Rhone Poulenc Chimie PREPARATION OF CARBOXYLIC ACIDS OR CORRESPONDING ESTERS BY CARBONYLATION IN THE PRESENCE OF IRIDIUM
US5510524A (en) * 1995-02-21 1996-04-23 Bp Chemicals Limited Process for the production of a carboxylic acid

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