GB2015509A - Recovery of methacrylic acid and alcohol in methacrylate production process - Google Patents

Recovery of methacrylic acid and alcohol in methacrylate production process

Info

Publication number
GB2015509A
GB2015509A GB7906677A GB7906677A GB2015509A GB 2015509 A GB2015509 A GB 2015509A GB 7906677 A GB7906677 A GB 7906677A GB 7906677 A GB7906677 A GB 7906677A GB 2015509 A GB2015509 A GB 2015509A
Authority
GB
United Kingdom
Prior art keywords
zone
methacrylic acid
separating
solution
alcohol
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
GB7906677A
Other versions
GB2015509B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co 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
Priority claimed from JP2302978A external-priority patent/JPS54115318A/en
Priority claimed from JP3034178A external-priority patent/JPS54122209A/en
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of GB2015509A publication Critical patent/GB2015509A/en
Application granted granted Critical
Publication of GB2015509B publication Critical patent/GB2015509B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/48Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/08Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds

Landscapes

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

Abstract

Methacrylic acid esters are effectively obtained from a feedstock dilute aqueous solution of methacrylic acid containing by-produced acetic acid and others, obtained by gas phase catalytic oxidation of isobutylene, tert.butyl alcohol or methacrolein, by (1) subjecting said feedstock to extraction in a methacrylic acid extracting zone (a), (2) separating the resulting extract solution into two fractions by distillation in an extracting solvent- separating zone (b), (3) esterifying the resulting methacrylic acid solution with a low-boiling alcohol in the presence of an acid catalyst in an esterification zone (c), while removing water by azeotropic distillation, (4) separating the solution discharged from the bottom of the esterification zone (c) into a product containing layer and an aqueous catalyst containing layer in a decanting zone (d), (5) recycling the aqueous layer to the esterification zone (c) after separating by-produced polymerization products therefrom, (6) joining the product layer with the distillate from step (3), (7) recovering unreacted alcohol from the resulting mixture by extraction in an extraction zone (e), (8) recycling the alcohol to the esterification zone (c), (9) distilling low boiling materials from a raffinate phase leaving the top of the extraction zones (e), (10) separating the raffinate phase into a high purity methacrylic acid ester product and an unreacted methacrylic acid solution, and (11) recycling this solution to zone (a) in step (1) or to step (2).
GB7906677A 1978-02-28 1979-02-26 Recovery of methacrylic acid and alcohol in methacrylate production process Expired GB2015509B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2302978A JPS54115318A (en) 1978-02-28 1978-02-28 Recovery of methacrylic acid
JP3034178A JPS54122209A (en) 1978-03-15 1978-03-15 Recovery of unsaturated aliphatic acid and alcohol

Publications (2)

Publication Number Publication Date
GB2015509A true GB2015509A (en) 1979-09-12
GB2015509B GB2015509B (en) 1982-08-25

Family

ID=26360319

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7906677A Expired GB2015509B (en) 1978-02-28 1979-02-26 Recovery of methacrylic acid and alcohol in methacrylate production process

Country Status (6)

Country Link
CA (1) CA1131657A (en)
DE (1) DE2907602A1 (en)
FR (1) FR2418216B1 (en)
GB (1) GB2015509B (en)
IT (1) IT1114704B (en)
NL (1) NL7901502A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4474981A (en) * 1981-08-11 1984-10-02 Sumitomo Chemical Company, Limited Process for preparing an acrylic or methacrylic acid ester
US7777085B2 (en) 2008-10-01 2010-08-17 Inventure Chemical, Inc. Method for conversion of oil-containing algae to 1,3-propanediol
CN111807960A (en) * 2020-08-01 2020-10-23 浙江亦龙新材料有限公司 Preparation process of isooctyl acrylate

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7943792B2 (en) 2007-04-02 2011-05-17 Inventure Chemical Inc. Production of biodiesel, cellulosic sugars, and peptides from the simultaneous esterification and alcoholysis/hydrolysis of materials with oil-containing substituents including phospholipids and peptidic content
WO2008122029A1 (en) 2007-04-02 2008-10-09 Inventure Chemical, Inc. Simultaneous esterification and alcohol ysis/hydrolysis of oil-containing materials with cellulosic and peptidic content

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1393173A (en) * 1963-05-16 1965-03-19 Distillers Co Yeast Ltd Ethyl acrylate production process
GB1257399A (en) * 1970-07-04 1971-12-15

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4474981A (en) * 1981-08-11 1984-10-02 Sumitomo Chemical Company, Limited Process for preparing an acrylic or methacrylic acid ester
US7777085B2 (en) 2008-10-01 2010-08-17 Inventure Chemical, Inc. Method for conversion of oil-containing algae to 1,3-propanediol
CN111807960A (en) * 2020-08-01 2020-10-23 浙江亦龙新材料有限公司 Preparation process of isooctyl acrylate
CN111807960B (en) * 2020-08-01 2022-04-22 浙江亦龙新材料有限公司 Preparation process of isooctyl acrylate

Also Published As

Publication number Publication date
FR2418216B1 (en) 1986-02-14
CA1131657A (en) 1982-09-14
GB2015509B (en) 1982-08-25
FR2418216A1 (en) 1979-09-21
DE2907602A1 (en) 1979-09-06
NL7901502A (en) 1979-08-30
IT7948149A0 (en) 1979-02-27
IT1114704B (en) 1986-01-27

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Legal Events

Date Code Title Description
PE20 Patent expired after termination of 20 years

Effective date: 19990225