GB916551A - Continuous polymerization of n-vinyl heterocyclic monomers - Google Patents

Continuous polymerization of n-vinyl heterocyclic monomers

Info

Publication number
GB916551A
GB916551A GB889261A GB889261A GB916551A GB 916551 A GB916551 A GB 916551A GB 889261 A GB889261 A GB 889261A GB 889261 A GB889261 A GB 889261A GB 916551 A GB916551 A GB 916551A
Authority
GB
United Kingdom
Prior art keywords
vinyl
polymerization
isopropanol
aqueous
pyrrolidone
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.)
Expired
Application number
GB889261A
Inventor
John Forrest Voeks
Teddy Gene Traylor
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 to NL261943D priority Critical patent/NL261943A/xx
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Priority to DED35625A priority patent/DE1157397B/en
Priority to GB889261A priority patent/GB916551A/en
Priority to FR855457A priority patent/FR1291612A/en
Publication of GB916551A publication Critical patent/GB916551A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F26/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
    • C08F26/06Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

In a continuous process for the polymerization in aqueous media of N-vinyl heterocyclic monomers, cross linking and gelation are inhibited by the use of one or more polymerization modifiers chosen from isopropanol, thioglycolic acid, dimethyl formamide, ethanolamine, methyl ethyl ketone, trichloracetic acid and 2-mercapto ethanol. Heterocyclic monomers specified are N-vinyl lactam, N-vinyl caprolactam, N-vinyl-3-morpholinone, N-vinyl pyrrolidone, N-vinyl piperidone and N-vinyl-5-methyl pyrrolidone. These may be copolymerized with acrylic acid and its homologs, acrylic esters, methacrylonitrile, vinyl methyl ketone, vinyl chloride, styrene, or vinyl acetate. The polymerization may be initiated by azo catalysts such as azobisisobutyronitrile, peroxygen catalysts, such as hydrogen peroxide and potassium persulphate, or by use of high energy radiation. A polymerization vehicle may be prepared by mixing water with from 0,1 to 95% by weight of the polymerization modifier. To this vehicle may be added 5 to 50% by weight of the N-vinyl heterocyclic monomer according to the amount of any copolymerizable ethylenic monomer present. The polymerization mixture may be continuously passed through the reaction chamber, where it is mechanically stirred and maintained at a temperature of 25 DEG to 100 DEG C. The polymer may be recovered by spray drying or solvent stripping. In the examples N-vinyl pyrrolidone is polymerized in aqueous medium in the presence of (1) isopropanol, aqueous ammonium hydroxide and aqueous hydrogen peroxide; (2) isopropanol and azobisisobutyronitrile and (3) thioglycolic acid and X-rays.
GB889261A 1961-03-10 1961-03-10 Continuous polymerization of n-vinyl heterocyclic monomers Expired GB916551A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
NL261943D NL261943A (en) 1961-03-10
DED35625A DE1157397B (en) 1961-03-10 1961-03-10 Process for the polymerization of N-vinyl lactams
GB889261A GB916551A (en) 1961-03-10 1961-03-10 Continuous polymerization of n-vinyl heterocyclic monomers
FR855457A FR1291612A (en) 1961-03-10 1961-03-13 Continuous polymerization of heterocyclic n-vinyl monomers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB889261A GB916551A (en) 1961-03-10 1961-03-10 Continuous polymerization of n-vinyl heterocyclic monomers

Publications (1)

Publication Number Publication Date
GB916551A true GB916551A (en) 1963-01-23

Family

ID=9861307

Family Applications (1)

Application Number Title Priority Date Filing Date
GB889261A Expired GB916551A (en) 1961-03-10 1961-03-10 Continuous polymerization of n-vinyl heterocyclic monomers

Country Status (2)

Country Link
GB (1) GB916551A (en)
NL (1) NL261943A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020118780A1 (en) * 2018-12-14 2020-06-18 中国科学院广州能源研究所 Hydrate kinetics inhibitor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020118780A1 (en) * 2018-12-14 2020-06-18 中国科学院广州能源研究所 Hydrate kinetics inhibitor
US11919978B2 (en) 2018-12-14 2024-03-05 Guangzhou Institute Of Energy Conversion, Chinese Academy Of Sciences Hydrate kinetics inhibitor

Also Published As

Publication number Publication date
NL261943A (en)

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