GB1093472A - Anionic polymerisation process - Google Patents

Anionic polymerisation process

Info

Publication number
GB1093472A
GB1093472A GB15565A GB15565A GB1093472A GB 1093472 A GB1093472 A GB 1093472A GB 15565 A GB15565 A GB 15565A GB 15565 A GB15565 A GB 15565A GB 1093472 A GB1093472 A GB 1093472A
Authority
GB
United Kingdom
Prior art keywords
ethylenically unsaturated
conjugated
halogen atom
compounds
polyolefines
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
GB15565A
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.)
Monsanto Co
Original Assignee
Monsanto 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 Monsanto Co filed Critical Monsanto Co
Publication of GB1093472A publication Critical patent/GB1093472A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C19/00Chemical modification of rubber
    • C08C19/30Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
    • C08C19/42Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
    • C08C19/44Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
    • 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
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/02Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
    • C08F297/023Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type using a coupling agent

Abstract

Polymers of ethylenically unsaturated monomers are produced by (a) polymerizing said monomer in the presence of an anionic polymerization catalyst and an inert liquid medium to a predetermined average molecular weight and then (b) adding to the resulting polymerization system an organic compound containing at least one halogen atom and at least one ethylenically unsaturated group or a plurality of non-conjugated ethylenically unsaturated groups. In stage (b) the organic compounds containing at least one halogen atom and at least one ethylenically unsaturated group may have the general formula (Y)n-R-(X)m, in which R is a hydrocarbon group having 1 to 20 carbon atoms, X is a halogen atom, Y is an ethylenically unsaturated group in which the ethylenically unsaturated linkage is in the terminal position and "m" and "n" are each integers of at least 1. Examples given are the nuclear substituted halostyrenes, the nuclear substituted haloalkyl styrenes, halogenated poly-ethylenically unsaturated compounds such as 1-chloro-3,5-divinyl benzene, halogenated a -olefines and polyolefines such as 3-chloropropene-1 and chloroprene, and vinyl benzyl halides. The organic compounds containing a plurality of non - conjugated ethylenically unsaturated groups may have the general formula R-(X)n in which R and X are as above and "n" is an integer which is at least 2. Examples given are aromatic polyvinyl compounds such as the divinyl and trivinyl benzenes and the diallyl and triallyl benzenes, aliphatic non-conjugated polyolefines such as pentadiene-1,4 and polyethylenically unsaturated esters such as ethylene glycol dimethacrylate. The ethylenically unsaturated monomers, the anionic initiators and the liquid solvents may be styrene or alkyl or alkoxy substituted styrenes, conjugated diolefines, or acrylic or methacrylic esters; alkali metals and alkyl and aryl compounds thereof; and hydrocarbons, ethers and amides. In the examples stage (a) is carried out by polymerizing separately butadiene, styrene and methyl methacrylate using butyl lithium or sodium naphthalene as catalyst.
GB15565A 1964-01-02 1965-01-01 Anionic polymerisation process Expired GB1093472A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US33540564A 1964-01-02 1964-01-02
US33535864A 1964-01-02 1964-01-02

Publications (1)

Publication Number Publication Date
GB1093472A true GB1093472A (en) 1967-12-06

Family

ID=26989658

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15565A Expired GB1093472A (en) 1964-01-02 1965-01-01 Anionic polymerisation process

Country Status (3)

Country Link
DE (1) DE1570937A1 (en)
FR (1) FR1447176A (en)
GB (1) GB1093472A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2201301A1 (en) * 1972-10-02 1974-04-26 Goodyear Tire & Rubber

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1432782A (en) * 1972-04-14 1976-04-22 Cpc International Inc Polymers and processes therefor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2201301A1 (en) * 1972-10-02 1974-04-26 Goodyear Tire & Rubber

Also Published As

Publication number Publication date
FR1447176A (en) 1966-07-29
DE1570937A1 (en) 1969-12-11

Similar Documents

Publication Publication Date Title
GB1241891A (en) Organic peroxy compounds
GB1096912A (en) Synthetic polymers
GB816510A (en) Boron-removing resin and process for removing boron compounds from fluids
KR910020056A (en) Star block polymer and preparation method thereof
GB1093472A (en) Anionic polymerisation process
Mizote et al. Cationic polymerization α, β‐disubstituted olefins. Part I. Cationic copolymerization of β‐methylstyrenes
EP0610515A4 (en) Process for producing polymer.
GB948693A (en) Novel tertiary phosphine and process of preparation
Miller et al. Polymerization of tert‐butyl crotonate
GB1023890A (en) Process for preparing high impact resinous composition
GB1336468A (en) Polymerizable compositions
GB987353A (en) Process for the production of graft polymers
US3170899A (en) Copolymers of olefinic compounds with p-tertiary alkyl phenyl acrylates and isomers thereof
GB1005407A (en) Production of reactive free radicals and novel dibenzyl compounds
ES295430A1 (en) Process for preparing polymers using a catalyst system comprising arylethylene oxide, polymeric vinyl aromatic peroxide and monocarboxylic acid
Mizote et al. Cationic polymerization of the geometrical isomers of β‐methylstyrene and anethole
ITMI962203A1 (en) PROCESS FOR THE PRODUCTION OF VINYLAROMATIC POLYMERS WITH A HIGH DEGREE OF SYNDIOTAXY
GB1094557A (en) Polymers of unsaturated tertiary amines
Imoto et al. Polymerization of methyl methacrylate initiated with vanillin
Sato et al. Macromonomer synthesis using α‐(2‐methyl‐2‐phenylpropyl) acrylates as addition–fragmentation chain‐transfer agents expelling the cumyl radical
US3127383A (en) x xocor
JPS55145712A (en) Novel high-molecular compound having phase transfer catalytic effect and preparation thereof
JPS52151383A (en) Preparation of styrene polymers
Butler et al. Linear polymers from diene monomers by the cyclic polymerization mechanism. XI. Polyphosphonium salts via cyclopolymerization
Kobayashi et al. Preparation of styrene derivatives containing sulfide group: addition reactions of thiophenol and its derivatives to 1, 4-divinylbenzene