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Precipitation polymerization of 1:1 copolymerizates of maleic acid anhydride and allyl acetate

Assignee: Consortium fuer Elektrochemische Industrie GmbH
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Filing: 1973-06-11
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Granted: 1975-06-03
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Expires: 1993-06-11
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Abstract

Abstract This invention relates to a method of precipitation polymerization of 1:1 copolymerizates of maleic acid anhydride and allyl acetate consisting of polymerizing a solution of a monomer mixture of maleic acid anhydride and allyl acetate in an organic diluent in which said monomer mixture is soluble but the copolymer produced is substantially insoluble in the presence of at least one suspension aid and a free-radical-former selected from the group consisting of dialkyl peroxydicarbonates, dicycloalkyl peroxydicarbonates and lower alkyl esters of peracids at a temperature and time sufficient to effect polymerization, and recovering a 1:1 copolymerizate of maleic acid anhydride and allyl acetate.

Inventors

  • 👤 Karlheinz Lottes
  • 👤 Hans Katzer

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 15:58
CPC Classifications
C; C08; C08F; C08F18/00; C08F18/02; C08F18/12; C08F22/00; C08F22/04

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 98 words
A METHOD OF PRECIPITATION POLYMERIZATION OF 1:1 COPOLYMERIZATES OF MALEIC ACID ANHYDRIDE AND ALKYL ACETATE CONSISTING OF POLYMERIZING A SOLUTION OF A MONOMER MIXTURE OF MALEIC ACID ANHYDRIDE AND ALKYL ACETATE IN AN ORGANIC DILUENT IN WHICH SAID MONOMER MIXTURE IS SOLUBLE BUT THE COPOLYMER PRODUCED IS SUBSTANTIALLY INSOLUBLE IN THE PRESENCE OF AT LEAST ONE SUSPENSION AID AND A FREE-RADICAL-FORMER SELECTED FROM THE GROUP CONSISTING OF DIALKYL PEROXYDICARBONATES, DICYCLOALKYL PEROXYDICARBONATES AND LOWER ALKYL ESTERS OF PERACIDS AT A TEMPERATURE AND TIME SUFFICIENT TO EFFECT POLYMERIZATION, AND RECOVERING A 1:1 COPOLYMERIZATE OF MALEIC ACID ANHYDRIDE AND ALLYL ACETATE.
Claim 2
Independent Claim 98 words
A METHOD OF PRECIPITATION POLYMERIZATION OF 1:1 COPOLYMERIZATES OF MALEIC ACID ANHYDRIDE AND ALKYL ACETATE CONSISTING OF POLYMERIZING A SOLUTION OF A MONOMER MIXTURE OF MALEIC ACID ANHYDRIDE AND ALKYL ACETATE IN AN ORGANIC DILUENT IN WHICH SAID MONOMER MIXTURE IS SOLUBLE BUT THE COPOLYMER PRODUCED IS SUBSTANTIALLY INSOLUBLE IN THE PRESENCE OF AT LEAST ONE SUSPENSION AID AND A FREE-RADICAL-FORMER SELECTED FROM THE GROUP CONSISTING OF DIALKYL PEROXYDICARBONATES, DICYCLOALKYL PEROXYDICARBONATES AND LOWER ALKYL ESTERS OF PERACIDS AT A TEMPERATURE AND TIME SUFFICIENT TO EFFECT POLYMERIZATION, AND RECOVERING A 1:1 COPOLYMERIZATE OF MALEIC ACID ANHYDRIDE AND ALLYL ACETATE.
Claim 3
Independent Claim 98 words
A method of precipitation polymerization of 1:1 copolymerizates of maleic acid anhydride and allyl acetate consisting of polymerizing a solution of a monomer mixture of maleic acid anhydride and allyl acetate in an organic diluent in which said monomer mixture is soluble but the copolymer produced is substantially insoluble in the presence of at least one suspension aid and a free-radical-former selected from the group consisting of dialkyl peroxydicarbonates, dicycloalkyl peroxydicarbonates and lower alkyl esters of peracids at a temperature and time sufficient to effect polymerization, and recovering a 1:1 copolymerizate of maleic acid anhydride and allyl acetate.
Claim 4
Independent Claim 98 words
A method of precipitation polymerization of 1:1 copolymerizates of maleic acid anhydride and allyl acetate consisting of polymerizing a solution of a monomer mixture of maleic acid anhydride and allyl acetate in an organic diluent in which said monomer mixture is soluble but the copolymer produced is substantially insoluble in the presence of at least one suspension aid and a free-radical-former selected from the group consisting of dialkyl peroxydicarbonates, dicycloalkyl peroxydicarbonates and lower alkyl esters of peracids at a temperature and time sufficient to effect polymerization, and recovering a 1:1 copolymerizate of maleic acid anhydride and allyl acetate.
Claim 5
Dependent Claim 16 words
The method of claim 1 wherein said monomer mixture is employed in a substantially equimolar ratio.
Claim 6
Dependent Claim 25 words
The method of claim 1 wherein said organic diluent is employed in a weight ratio of diluent to monomer mixture of from 0.5:1 to 4:1.
Claim 7
Dependent Claim 16 words
The method of claim 3, wherein said weight ratio of diluent to monomer mixture is 2:1.
Claim 8
Dependent Claim 37 words
The method of claim 1 wherein said at least one suspension aid is soluble in said organic diluent and is employed in amounts of from 0.01 to 1% by weight, based on the weight of the monomers.
Claim 9
Dependent Claim 24 words
The method of claim 5 wherein said suspension aid is a member selected from the group consisting of polyvinyl lower alkyl ethers and polystyrene.
Claim 10
Dependent Claim 33 words
The method of claim 5 wherein said suspension aid is a polyvinyl lower alkyl ether employed in an amount of from 0.25 to 0.25% by weight, based on the weight of the monomers.
Claim 11
Dependent Claim 15 words
The method of claim 7 wherein said polyvinyl lower alkyl ether is polyvinyl ethyl ether.
Claim 12
Dependent Claim 29 words
The method of claim 5 wherein said suspension aid is polystyrene employed in an amount of from 0.1 to 0.5% by weight, based on the weight of the monomers.
Claim 13
Dependent Claim 27 words
The method of claim 9 wherein said polystyrene is employed in an amount of from 0.15 to 0.25% by weight, based on the weight of the monomers.
Claim 14
Dependent Claim 27 words
The method of claim 1 wherein said free-radical-formers are employed in an amount of from 0.01 to 5% by weight, based on the weight of the monomers.
Claim 15
Dependent Claim 27 words
The method of claim 11 wherein said free-radical-formers are employed in an amount of from 0.5 to 2% by weight, based on the weight of the monomers.
Claim 16
Dependent Claim 14 words
The method of claim 1 wherein said temperature is maintained between 5* and 140*C.

References Cited (Backward Citations)

US2464062A Cited
US2562852A Cited
US2522775A Cited
US3218302A Cited
US3553183A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-06-02 1978-12-02 1979-06-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-06-02 1982-12-02 1983-06-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-06-02 1986-12-02 1987-06-03 $7700.00 Window Closed / Lapsed

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