Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol
The invention relates to thermotropic liquid crystalline polymer compositions of the general formula: -(CO-C6H4O)m-(CO-C6H4-CO)n -(O-C6H4-X)p-(O-C6H4-C(CH3)2-C6H4-O)q-(O-C6H4-S-C6H4-O)t- where substantially all aromatic substituents are para to one another, where -X- can be either -O- or -NH-, and m...
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creator | BLAIR EDGAR A GRAHAM SUE H WILSON DONALD R |
description | The invention relates to thermotropic liquid crystalline polymer compositions of the general formula: -(CO-C6H4O)m-(CO-C6H4-CO)n -(O-C6H4-X)p-(O-C6H4-C(CH3)2-C6H4-O)q-(O-C6H4-S-C6H4-O)t- where substantially all aromatic substituents are para to one another, where -X- can be either -O- or -NH-, and m, n, p, q and t are mole fractions totaling 1.0, where m is 0 to 0.75, m plus 2p is 0.5 to 0.75, n is 0.125 to 0.5, p is 0 to 0.375, q is 0.125 to 0.25, n equals p plus q plus t, and t is greater than 0.0125, but equal to no greater than 90% of q plus t. Preferably X is -O-, m is from 0.5 to 0.75 and p is less than 0.05. Alternatively, m is less than 0.1 and p is from 0.25 to 0.375. The thermotropic liquid crystalline polymer composition is the reaction product of the copolymerization of: a) p-Hydroxybenzoic acid, b) a member selected from the group consisting of hydroquinone and p-aminophenol, c) Bisphenol A, d) 4,4'-thiodiphenol, and e) terephthalic acid, wherein the thiodiphenol is present in an amount at least equal to 1.25 mole % of the total composition, the Bisphenol A is present in an amount at least equal to 12.5 mole %, and the concentration of the thiodiphenol plus Bisphenol A is up to about 25 mole %. |
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Preferably X is -O-, m is from 0.5 to 0.75 and p is less than 0.05. Alternatively, m is less than 0.1 and p is from 0.25 to 0.375. The thermotropic liquid crystalline polymer composition is the reaction product of the copolymerization of: a) p-Hydroxybenzoic acid, b) a member selected from the group consisting of hydroquinone and p-aminophenol, c) Bisphenol A, d) 4,4'-thiodiphenol, and e) terephthalic acid, wherein the thiodiphenol is present in an amount at least equal to 1.25 mole % of the total composition, the Bisphenol A is present in an amount at least equal to 12.5 mole %, and the concentration of the thiodiphenol plus Bisphenol A is up to about 25 mole %.</description><language>eng</language><subject>ADHESIVES ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; DYES ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC MACROMOLECULAR COMPOUNDS ; PAINTS ; POLISHES ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1992</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=19921222&DB=EPODOC&CC=US&NR=5173562A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19921222&DB=EPODOC&CC=US&NR=5173562A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BLAIR; EDGAR A</creatorcontrib><creatorcontrib>GRAHAM; SUE H</creatorcontrib><creatorcontrib>WILSON; DONALD R</creatorcontrib><title>Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol</title><description>The invention relates to thermotropic liquid crystalline polymer compositions of the general formula: -(CO-C6H4O)m-(CO-C6H4-CO)n -(O-C6H4-X)p-(O-C6H4-C(CH3)2-C6H4-O)q-(O-C6H4-S-C6H4-O)t- where substantially all aromatic substituents are para to one another, where -X- can be either -O- or -NH-, and m, n, p, q and t are mole fractions totaling 1.0, where m is 0 to 0.75, m plus 2p is 0.5 to 0.75, n is 0.125 to 0.5, p is 0 to 0.375, q is 0.125 to 0.25, n equals p plus q plus t, and t is greater than 0.0125, but equal to no greater than 90% of q plus t. Preferably X is -O-, m is from 0.5 to 0.75 and p is less than 0.05. Alternatively, m is less than 0.1 and p is from 0.25 to 0.375. The thermotropic liquid crystalline polymer composition is the reaction product of the copolymerization of: a) p-Hydroxybenzoic acid, b) a member selected from the group consisting of hydroquinone and p-aminophenol, c) Bisphenol A, d) 4,4'-thiodiphenol, and e) terephthalic acid, wherein the thiodiphenol is present in an amount at least equal to 1.25 mole % of the total composition, the Bisphenol A is present in an amount at least equal to 12.5 mole %, and the concentration of the thiodiphenol plus Bisphenol A is up to about 25 mole %.</description><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>DYES</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>NATURAL RESINS</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>PAINTS</subject><subject>POLISHES</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1992</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFyrsOwjAMheEuDAh4Bryx0AHawlwhEAMbMEdpaoilxA5NEOrbc92Zzi-db5ipA93u1ILp-pi0gyCu99iBER8kUiLhV3PSxMRXaCgGiywOaqD34xti_VEPShbKeTnLkyVp6evG2eCiXcTJb0fZdLc9bfY5BlEYgzbImNT5WC3WRbVa1sV_8QS8TTxU</recordid><startdate>19921222</startdate><enddate>19921222</enddate><creator>BLAIR; EDGAR A</creator><creator>GRAHAM; SUE H</creator><creator>WILSON; DONALD R</creator><scope>EVB</scope></search><sort><creationdate>19921222</creationdate><title>Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol</title><author>BLAIR; EDGAR A ; GRAHAM; SUE H ; WILSON; DONALD R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US5173562A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1992</creationdate><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>DYES</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>NATURAL RESINS</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>PAINTS</topic><topic>POLISHES</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>BLAIR; EDGAR A</creatorcontrib><creatorcontrib>GRAHAM; SUE H</creatorcontrib><creatorcontrib>WILSON; DONALD R</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BLAIR; EDGAR A</au><au>GRAHAM; SUE H</au><au>WILSON; DONALD R</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol</title><date>1992-12-22</date><risdate>1992</risdate><abstract>The invention relates to thermotropic liquid crystalline polymer compositions of the general formula: -(CO-C6H4O)m-(CO-C6H4-CO)n -(O-C6H4-X)p-(O-C6H4-C(CH3)2-C6H4-O)q-(O-C6H4-S-C6H4-O)t- where substantially all aromatic substituents are para to one another, where -X- can be either -O- or -NH-, and m, n, p, q and t are mole fractions totaling 1.0, where m is 0 to 0.75, m plus 2p is 0.5 to 0.75, n is 0.125 to 0.5, p is 0 to 0.375, q is 0.125 to 0.25, n equals p plus q plus t, and t is greater than 0.0125, but equal to no greater than 90% of q plus t. Preferably X is -O-, m is from 0.5 to 0.75 and p is less than 0.05. Alternatively, m is less than 0.1 and p is from 0.25 to 0.375. The thermotropic liquid crystalline polymer composition is the reaction product of the copolymerization of: a) p-Hydroxybenzoic acid, b) a member selected from the group consisting of hydroquinone and p-aminophenol, c) Bisphenol A, d) 4,4'-thiodiphenol, and e) terephthalic acid, wherein the thiodiphenol is present in an amount at least equal to 1.25 mole % of the total composition, the Bisphenol A is present in an amount at least equal to 12.5 mole %, and the concentration of the thiodiphenol plus Bisphenol A is up to about 25 mole %.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ADHESIVES CHEMISTRY COMPOSITIONS BASED THEREON DYES MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NATURAL RESINS ORGANIC MACROMOLECULAR COMPOUNDS PAINTS POLISHES THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol |
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