Curing synthetic elastomers
Copolymers of butadiene and an alkyl acrylate or an alkyl acrylate having an electrophilic substituent in the alkyl group are cured by heating in the presence of a basic oxide or hydroxide of a polyvalent metal and a neutral or basic organic hydroxy compound. The copolymers may contain 5-60% by weig...
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creator | DAVEY WALTER CECIL BIRD THEODORE BASSETT COOPER WILFRID |
description | Copolymers of butadiene and an alkyl acrylate or an alkyl acrylate having an electrophilic substituent in the alkyl group are cured by heating in the presence of a basic oxide or hydroxide of a polyvalent metal and a neutral or basic organic hydroxy compound. The copolymers may contain 5-60% by weight of monomers of alkyl acrylate which preferably contains up to 4 carbon atoms in the alkyl group. Suitable negative substituents in the alkyl group are chlorine, bromine, cyano, nitro-, or sulphonic groups. The copolymer may contain up to 30% of a third monomer containing a vinylidene group such as methyl methacrylate, vinylidene chloride, methyl isopropenyl ketone, methyl vinyl ketone, acrylonitrile and styrene. The copolymers are prepared by emulsion polymerization using a persulphate or redox catalyst. The preferred organic hydroxy compounds are those which will dissolve at least 0,1% of the basic oxide or hydroxide used and are preferably aliphatic or have a predominantly aliphatic nature, preferably have a boiling point above the curing temperature, and include starches, glucose, sorbitol, mannitol, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, glycerol, tetramethylol cyclohexanol, transquinitol, 1,5-bis(2-hydroxyethyl) naphthalene cyclohexanol, benzyl alcohol and lauryl alcohol. It is used in an amount of 1-15% by weight of the copolymer. The basic oxide or hydroxide is preferably one of a divalent metal such as an alkaline earth metal and is used in an amount of 5-10% by weight of the copolymer. Curing times are 30 minutes to 4 hours at about 150 DEG C. Carbon black or titanium dioxide fillers may be added but acidic ingredients should be avoided. Specification 808,913 is referred to. |
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The copolymers may contain 5-60% by weight of monomers of alkyl acrylate which preferably contains up to 4 carbon atoms in the alkyl group. Suitable negative substituents in the alkyl group are chlorine, bromine, cyano, nitro-, or sulphonic groups. The copolymer may contain up to 30% of a third monomer containing a vinylidene group such as methyl methacrylate, vinylidene chloride, methyl isopropenyl ketone, methyl vinyl ketone, acrylonitrile and styrene. The copolymers are prepared by emulsion polymerization using a persulphate or redox catalyst. The preferred organic hydroxy compounds are those which will dissolve at least 0,1% of the basic oxide or hydroxide used and are preferably aliphatic or have a predominantly aliphatic nature, preferably have a boiling point above the curing temperature, and include starches, glucose, sorbitol, mannitol, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, glycerol, tetramethylol cyclohexanol, transquinitol, 1,5-bis(2-hydroxyethyl) naphthalene cyclohexanol, benzyl alcohol and lauryl alcohol. It is used in an amount of 1-15% by weight of the copolymer. The basic oxide or hydroxide is preferably one of a divalent metal such as an alkaline earth metal and is used in an amount of 5-10% by weight of the copolymer. Curing times are 30 minutes to 4 hours at about 150 DEG C. Carbon black or titanium dioxide fillers may be added but acidic ingredients should be avoided. Specification 808,913 is referred to.</description><language>eng</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; COMPOSITIONS OF MACROMOLECULAR COMPOUNDS ; METALLURGY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</subject><creationdate>1960</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19601012&DB=EPODOC&CC=GB&NR=851045A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19601012&DB=EPODOC&CC=GB&NR=851045A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>DAVEY WALTER CECIL</creatorcontrib><creatorcontrib>BIRD THEODORE BASSETT</creatorcontrib><creatorcontrib>COOPER WILFRID</creatorcontrib><title>Curing synthetic elastomers</title><description>Copolymers of butadiene and an alkyl acrylate or an alkyl acrylate having an electrophilic substituent in the alkyl group are cured by heating in the presence of a basic oxide or hydroxide of a polyvalent metal and a neutral or basic organic hydroxy compound. The copolymers may contain 5-60% by weight of monomers of alkyl acrylate which preferably contains up to 4 carbon atoms in the alkyl group. Suitable negative substituents in the alkyl group are chlorine, bromine, cyano, nitro-, or sulphonic groups. The copolymer may contain up to 30% of a third monomer containing a vinylidene group such as methyl methacrylate, vinylidene chloride, methyl isopropenyl ketone, methyl vinyl ketone, acrylonitrile and styrene. The copolymers are prepared by emulsion polymerization using a persulphate or redox catalyst. The preferred organic hydroxy compounds are those which will dissolve at least 0,1% of the basic oxide or hydroxide used and are preferably aliphatic or have a predominantly aliphatic nature, preferably have a boiling point above the curing temperature, and include starches, glucose, sorbitol, mannitol, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, glycerol, tetramethylol cyclohexanol, transquinitol, 1,5-bis(2-hydroxyethyl) naphthalene cyclohexanol, benzyl alcohol and lauryl alcohol. It is used in an amount of 1-15% by weight of the copolymer. The basic oxide or hydroxide is preferably one of a divalent metal such as an alkaline earth metal and is used in an amount of 5-10% by weight of the copolymer. Curing times are 30 minutes to 4 hours at about 150 DEG C. Carbon black or titanium dioxide fillers may be added but acidic ingredients should be avoided. 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The copolymers may contain 5-60% by weight of monomers of alkyl acrylate which preferably contains up to 4 carbon atoms in the alkyl group. Suitable negative substituents in the alkyl group are chlorine, bromine, cyano, nitro-, or sulphonic groups. The copolymer may contain up to 30% of a third monomer containing a vinylidene group such as methyl methacrylate, vinylidene chloride, methyl isopropenyl ketone, methyl vinyl ketone, acrylonitrile and styrene. The copolymers are prepared by emulsion polymerization using a persulphate or redox catalyst. The preferred organic hydroxy compounds are those which will dissolve at least 0,1% of the basic oxide or hydroxide used and are preferably aliphatic or have a predominantly aliphatic nature, preferably have a boiling point above the curing temperature, and include starches, glucose, sorbitol, mannitol, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, glycerol, tetramethylol cyclohexanol, transquinitol, 1,5-bis(2-hydroxyethyl) naphthalene cyclohexanol, benzyl alcohol and lauryl alcohol. It is used in an amount of 1-15% by weight of the copolymer. The basic oxide or hydroxide is preferably one of a divalent metal such as an alkaline earth metal and is used in an amount of 5-10% by weight of the copolymer. Curing times are 30 minutes to 4 hours at about 150 DEG C. Carbon black or titanium dioxide fillers may be added but acidic ingredients should be avoided. Specification 808,913 is referred to.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON COMPOSITIONS OF MACROMOLECULAR COMPOUNDS METALLURGY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS |
title | Curing synthetic elastomers |
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