GB1314096A - Elastomers - Google Patents
ElastomersInfo
- Publication number
- GB1314096A GB1314096A GB2484370A GB2484370A GB1314096A GB 1314096 A GB1314096 A GB 1314096A GB 2484370 A GB2484370 A GB 2484370A GB 2484370 A GB2484370 A GB 2484370A GB 1314096 A GB1314096 A GB 1314096A
- Authority
- GB
- United Kingdom
- Prior art keywords
- monomer
- acrylate
- weight
- acrylates
- stage
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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)
- Paints Or Removers (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
1314096 Acrylic block polymers ROHM & HAASCO 22 May 1970 [26 May 1969] 24843/70 Heading C3P A process for the production of vulcanizable acrylic elastomers comprises, in a first stage, polymerizing, in suspension or emulsion in a liquid medium, an initial monomer charge containing (i) at least 45% by weight, based on the weight of the charge, of an alkyl acrylate monomer, the homopolymer of which has a glass transition temperature below - 35‹ C., or a mixture of alkyl acrylate monomers, the copolymer of which has a glass transition temperature below - 35‹ C., (ii) from 0-5% by weight of a polyethylenically unsaturated monomer, (iii) from 0-10% by weight of a curing site-containing monomer, and (iv) from 0-50% by weight of at least one monomer selected from alkoxyalkyl acrylates, alkylthioalkyl acrylates, cyanoalkoxyalkyl acrylates and nitrile-substituted alkyl acrylates; and, in a subsequent and final stage, polymerizing in contact with the suspended polymer product of the preceding stage a final monomer charge containing (i) at least 60% by weight, based on the weight of the final monomer charge, of ethyl and/or methyl acrylate, (ii) 0-40% by weight of one or more other alkyl acrylates or substituted alkyl acrylates, (iii) 0- 40% by weight of a nitrile-containing monomer, and (iv) 0-10% by weight of curing sitecontaining monomer. The preferred alkyl acrylates are butyl, hexyl and/or 2-ethylhexyl acrylate; the polyethylenically unsaturated monomer may be butylene diacrylate, butylene dimethacrylate or divinyl benzene; other monomers may be 2-methoxyethyl acrylate, 2- ethoxyethyl acrylate, 2-ethyl-thioethyl acrylate, 4-cyanobutyl acrylate and/or 2-cyanoethyl acrylate, and the curing site-containing monomer may be 2-chloroethyl-vinyl ether, vinyl chloroacetate, beta-(chloroacetoxy)-ethyl-methacrylate and/or 4-chloro-2-buten-1-yl acrylate. Between the first and final polymerization stages may be interposed at least one intermediate polymerization stage in which an intermediate monomer charge is polymerized in contact with the suspended polymer product of the first stage and before polymerization of the final stage, the intermediate monomer charge containing (i) ethyl acrylate and (ii) an alkyl acrylate monomer, the homopolymer of which has a glass transition temperature below - 35‹ C., and, optionally, (iii) a polyfunctional crosslinking monomer, a curing site-containing monomer or an oil-resistance improving monomer.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US82794569A | 1969-05-26 | 1969-05-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1314096A true GB1314096A (en) | 1973-04-18 |
Family
ID=25250541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2484370A Expired GB1314096A (en) | 1969-05-26 | 1970-05-22 | Elastomers |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE2025342A1 (en) |
FR (1) | FR2048789A5 (en) |
GB (1) | GB1314096A (en) |
-
1970
- 1970-05-22 GB GB2484370A patent/GB1314096A/en not_active Expired
- 1970-05-23 DE DE19702025342 patent/DE2025342A1/en active Pending
- 1970-05-25 FR FR7019013A patent/FR2048789A5/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE2025342A1 (en) | 1970-12-03 |
FR2048789A5 (en) | 1971-03-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |