GB883850A - Process for controlling the molecular weight of vinylidene chloride polymers - Google Patents

Process for controlling the molecular weight of vinylidene chloride polymers

Info

Publication number
GB883850A
GB883850A GB3280760A GB3280760A GB883850A GB 883850 A GB883850 A GB 883850A GB 3280760 A GB3280760 A GB 3280760A GB 3280760 A GB3280760 A GB 3280760A GB 883850 A GB883850 A GB 883850A
Authority
GB
United Kingdom
Prior art keywords
per cent
vinylidene chloride
carbon
perhalomethane
methane
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
GB3280760A
Inventor
Marion Ross Rector
William Elray Cohrs
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
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Priority to GB3280760A priority Critical patent/GB883850A/en
Publication of GB883850A publication Critical patent/GB883850A/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
    • C08F214/00Copolymers 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 halogen
    • C08F214/02Monomers containing chlorine
    • C08F214/04Monomers containing two carbon atoms
    • C08F214/08Vinylidene chloride

Landscapes

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

Abstract

A process for producing relatively low molecular weight copolymers of vinylidene and vinyl chlorides, containing at least 70 weight per cent of vinylidene chloride, comprises polymerizing the monomers in the presence of from 5,0 to 0,05 weight per cent of a perhalomethane chain-stopper having the general formula Y-C-X3 wherein Y is bromine or iodine and X is any halogen atom. Specified perhalomethanes are carbon tetrabromide, bromotrichloromethane, dibrodichloromethane, chlorotribromomethane, bromotrifluoromethane, dibromodifluoromethane, fluorotribromomethane, bromochlorodifluoromethane, carbon tetraiodide, bromotriiodomethane, dibromodiiodomethane, iodotribromomethane, chlorotriiodomethane, dichlorodiiodomethane, iodotrichloromethane, fluorotriiodomethane, difluorodiiodomethane and iodotrifluoromethane. Any known polymerization technique may be employed, but aqueous suspension using a water-dispersible granulating agent, such as a water-soluble cellulose ether, is preferred. The perhalomethane is preferably added to the monomer charge before dispersion in the aqueous phase. In examples, 68 parts of vinylidene chloride and 12 parts of vinyl chloride are copolymerized, using methyl cellulose as suspending agent and lauroyl peroxide as catalyst, in the presence of various chain-transfer agents. The effect of several of the above specified perhalomethanes on the per cent conversion and solution viscosity is compared with that of the following previously known chain-transfer agents: lauryl mercaptan, carbon tetrachloride, chlorodibromo methane, bromochloro methane and bromoform. Another example shows the effect of different amounts of carbon tetrabromide on the solution viscosity obtained in the above polymerization at 80% conversion.ALSO:A process for producing relatively low molecular weight copolymers of vinylidene and vinyl chlorides, containing at least 70 weight per cent of vinylidene chloride, comprises polymerising the monomers in the presence of from 5.0 to 0.05 weight per cent of a perhalomethane chainstopper having the general formula Y-C-X3 wherein Y is bromine or iodine and X is any halogen atom. Specified perhalo methanes are carbon tetrabromide, bromotrichloromethane, dibrodichloromethane, chlorotribromomethane, bromotrifluoromethane, dibromodifluoromethane, fluorotribromomethane, bromochlorodifluoromethane, carbon tetraiodide, bromotriiodomethane, dibromodiiodomethane, iodotribromomethane, chlorotriiodomethane, dichlorodiiodomethane, iodotrichloromethane, fluorotriiodomethane, difluorodiiodomethane and iodotrifluoromethane. Any known polymerisation technique may be employed but aqueous suspension using a water-dispersible granulating agent such as a water-soluble cellulose ether is preferred. The perhalomethane is preferably added to the monomer charge before dispersion in the aqueous phase. In examples 68 parts of vinylidene chloride and 12 parts of vinyl chloride are copolymerised, using methyl cellulose as suspendihg agent and lauroyl peroxide as catalyst, in the presence of various chain-transfer agents. The effect of several of the above specified perhalomethanes on the per cent conversion and solution viscosity is compared with that of the following previously known chain-transfer agents: lauryl mercaptan, carbon tetrachloride, chlorodibromo methane, bromochloro methane and bromoform. Another example shows the effect of different amounts of carbon tetrabromide on the solution viscosity obtained in the above polymerisation at 80% conversion.
GB3280760A 1960-09-23 1960-09-23 Process for controlling the molecular weight of vinylidene chloride polymers Expired GB883850A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3280760A GB883850A (en) 1960-09-23 1960-09-23 Process for controlling the molecular weight of vinylidene chloride polymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3280760A GB883850A (en) 1960-09-23 1960-09-23 Process for controlling the molecular weight of vinylidene chloride polymers

Publications (1)

Publication Number Publication Date
GB883850A true GB883850A (en) 1961-12-06

Family

ID=10344279

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3280760A Expired GB883850A (en) 1960-09-23 1960-09-23 Process for controlling the molecular weight of vinylidene chloride polymers

Country Status (1)

Country Link
GB (1) GB883850A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3937690A (en) * 1972-06-19 1976-02-10 Dynamit Nobel Aktiengesellschaft Process for the preparation of thermoplastically workable fluoro-olefin polymers
US4000356A (en) * 1972-06-19 1976-12-28 Dynamit Nobel Aktiengesellschaft Process for the preparation of thermoplastically workable fluoro-olefin polymers
US5003014A (en) * 1990-05-21 1991-03-26 Gaf Chemicals Corporation Process for making copolymers of maleic anhydride and a C1 -C4 alkyl vinyl ether having a predetermined specific viscosity

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3937690A (en) * 1972-06-19 1976-02-10 Dynamit Nobel Aktiengesellschaft Process for the preparation of thermoplastically workable fluoro-olefin polymers
US4000356A (en) * 1972-06-19 1976-12-28 Dynamit Nobel Aktiengesellschaft Process for the preparation of thermoplastically workable fluoro-olefin polymers
US5003014A (en) * 1990-05-21 1991-03-26 Gaf Chemicals Corporation Process for making copolymers of maleic anhydride and a C1 -C4 alkyl vinyl ether having a predetermined specific viscosity

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