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RU98108500A - METHOD FOR PRODUCING ISOPHTHALIC ACID - Google Patents

METHOD FOR PRODUCING ISOPHTHALIC ACID

Info

Publication number
RU98108500A
RU98108500A RU98108500/04A RU98108500A RU98108500A RU 98108500 A RU98108500 A RU 98108500A RU 98108500/04 A RU98108500/04 A RU 98108500/04A RU 98108500 A RU98108500 A RU 98108500A RU 98108500 A RU98108500 A RU 98108500A
Authority
RU
Russia
Prior art keywords
acetic acid
oxidation
stage
cooling
water
Prior art date
Application number
RU98108500/04A
Other languages
Russian (ru)
Other versions
RU2163592C2 (en
Inventor
В.Ф. Назимок
В.Н. Александров
Н.Н. Гончарова
В.П. Юрьев
А.А. Кудашов
А.В. Гончаров
Original Assignee
Открытое акционерное общество "Научно-исследовательский и проектный институт мономеров с опытным заводом"
Filing date
Publication date
Application filed by Открытое акционерное общество "Научно-исследовательский и проектный институт мономеров с опытным заводом" filed Critical Открытое акционерное общество "Научно-исследовательский и проектный институт мономеров с опытным заводом"
Priority to RU98108500A priority Critical patent/RU2163592C2/en
Priority claimed from RU98108500A external-priority patent/RU2163592C2/en
Publication of RU98108500A publication Critical patent/RU98108500A/en
Application granted granted Critical
Publication of RU2163592C2 publication Critical patent/RU2163592C2/en

Links

Claims (2)

1. Способ получения изофталевой кислоты (ИФК) путем жидкофазного окисления м-ксилола кислородсодержащим газом в уксуснокислой среде при повышенной температуре и давлении в присутствии катализаторов, состоящих из солей кобальта, марганца и бромидных соединений, регулирования содержания воды в зоне окисления с последующим доокислением примесей и обработкой уксусной кислотой с использованием рецикла маточных растворов после выделения ИФК из уксуснокислых растворов на I-ю или II стадию, отличающийся тем, что катализатор дополнительно содержит соли цинка, никеля или смесь указанных солей металлов [MT] при соотношении [Cо + Мп] : [MT] = 1:0,01oC0,2, а содержание воды в зоне окисления регулируют путем трехступенчатого охлаждения парогазовой смеси выходящей из реактора в условиях прямотока газа и сконденсировавшихся паров СН3СООН - Н2O - на первой и третьей ступенях и противотока на второй ступени в сочетании с процессом ректификации с последующим возвратом обезвоженного потока жидкой уксусной кислоты суммарно с первой и второй ступеней охлаждения в зону окисления, выводом из процесса обводненной уксусной кислоты с третьей ступени охлаждения в соотношении, обеспечивающем концентрацию воды в зоне реакции 4-10%.1. A method of producing isophthalic acid (IFC) by liquid-phase oxidation of m-xylene with an oxygen-containing gas in an acetic acid medium at elevated temperature and pressure in the presence of catalysts consisting of cobalt, manganese and bromide salts, regulating the water content in the oxidation zone, followed by further oxidation of impurities and treatment with acetic acid using recycle of the mother liquor after the separation of IFC from acetic acid solutions to the I or II stage, characterized in that the catalyst additionally contains neighs zinc, nickel salts or a mixture of the indicated metal salts [MT] with the ratio [Co + Mn]: [MT] = 1: 0.01 o C0.2, and the water content in the oxidation zone is controlled by three-stage cooling of the vapor-gas mixture leaving the reactor under the conditions of the direct flow of gas and condensed vapors CH 3 COOH - Н 2 O - at the first and third stages and counterflow at the second stage in combination with a rectification process with the subsequent return of the dehydrated stream of liquid acetic acid in total from the first and second stages of cooling to the oxidation zone, from the process watered acetic acid from the third stage of cooling in a ratio providing a concentration of water in the reaction zone of 4-10%. 2. Способ по п. 1, отличающийся тем, что обработку изофталевой кислоты после доокисления примесей проводят уксусной кислотой или уксусной кислотой и водой при температуре 170-230oС.2. The method according to p. 1, characterized in that the processing of isophthalic acid after the oxidation of impurities is carried out with acetic acid or acetic acid and water at a temperature of 170-230 o C.
RU98108500A 1998-04-30 1998-04-30 Method of preparing isophthalic acid RU2163592C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU98108500A RU2163592C2 (en) 1998-04-30 1998-04-30 Method of preparing isophthalic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU98108500A RU2163592C2 (en) 1998-04-30 1998-04-30 Method of preparing isophthalic acid

Publications (2)

Publication Number Publication Date
RU98108500A true RU98108500A (en) 2000-02-20
RU2163592C2 RU2163592C2 (en) 2001-02-27

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
RU98108500A RU2163592C2 (en) 1998-04-30 1998-04-30 Method of preparing isophthalic acid

Country Status (1)

Country Link
RU (1) RU2163592C2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9045408B2 (en) * 2011-12-29 2015-06-02 Uop Llc Process for oxidizing alkyl-aromatic compounds

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