Verfahren zur Herstellung von härtbaren, modifizierten Harzen auf der Grundlage von aromatischen Di- und/oder Polycarbonsäuren und Aminen
A process for making heat-hardenable polyesterimides comprises reacting 10 equivalents of an aromatic polycarboxylic acid with at least one pair of carboxyl groups in ortho position to each other with from 5 to 16 equivalents of di- and/or trihydric alcohols and from 5.5 0.5 equivalents of di-primar...
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creator | KOCH,GERHARD BORNHAUPT,BERND,V RATING,WILHELM,DR |
description | A process for making heat-hardenable polyesterimides comprises reacting 10 equivalents of an aromatic polycarboxylic acid with at least one pair of carboxyl groups in ortho position to each other with from 5 to 16 equivalents of di- and/or trihydric alcohols and from 5.5 0.5 equivalents of di-primary amines, amino acids and/or hydroxyamines, where for every 10 equivalents of difunctional compounds there are from 4 to 20, preferably from 6 to 15 equivalents of polyfunctional compounds, at temperatures of up to 250 DEG C., if desired in the presence of solvents and/or carriers, the reaction being continued until the product becomes clear. Dicarboxylic acids may be present in the reaction mixture. An ester of zirconic or titanic acid in an amount to provide 0.1 to 0.2 gram of titanium or zirconium for every 100 gram of the polyesterimide may be present in the reactants or may be reacted with the polyesterimide. The carboxylic acids may be wholly or partially replaced by their anhydrides or lower alkyl esters thereof. Specified carboxylic acids are trimellitic, pyromellitic and terephthalic acid. Specified polyols are ethylene glycol, diethylene glycol, 1: 2-propanediol, 2: 2-dimethyl-1: 3-propane diol, 4: 41-bis(hydroxyethoxy) diphenyl dimethyl methane, glycerine, trimethylol propane, trimethylol ethane and mixtures thereof. Specified amino compounds are phenylene diamine, 4: 41-diamino diphenyl, 4: 41-diamino diphenyl-methane, 4: 41-diamino dicyclohexyl-methane, 4: 41-diamino diphenyl ethers, diamino diphenyl sulphones, aminobenzoic acids, aminoethanol and amino phenols. |
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Dicarboxylic acids may be present in the reaction mixture. An ester of zirconic or titanic acid in an amount to provide 0.1 to 0.2 gram of titanium or zirconium for every 100 gram of the polyesterimide may be present in the reactants or may be reacted with the polyesterimide. The carboxylic acids may be wholly or partially replaced by their anhydrides or lower alkyl esters thereof. Specified carboxylic acids are trimellitic, pyromellitic and terephthalic acid. Specified polyols are ethylene glycol, diethylene glycol, 1: 2-propanediol, 2: 2-dimethyl-1: 3-propane diol, 4: 41-bis(hydroxyethoxy) diphenyl dimethyl methane, glycerine, trimethylol propane, trimethylol ethane and mixtures thereof. Specified amino compounds are phenylene diamine, 4: 41-diamino diphenyl, 4: 41-diamino diphenyl-methane, 4: 41-diamino dicyclohexyl-methane, 4: 41-diamino diphenyl ethers, diamino diphenyl sulphones, aminobenzoic acids, aminoethanol and amino phenols.</description><edition>1</edition><language>ger</language><subject>ADHESIVES ; BASIC ELECTRIC ELEMENTS ; CABLES ; CHEMICAL PAINT OR INK REMOVERS ; CHEMISTRY ; COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS ; COMPOSITIONS BASED THEREON ; CONDUCTORS ; CORRECTING FLUIDS ; DYES ; ELECTRICITY ; FILLING PASTES ; INKS ; INSULATORS ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC MACROMOLECULAR COMPOUNDS ; PAINTS ; PASTES OR SOLIDS FOR COLOURING OR PRINTING ; POLISHES ; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING ORDIELECTRIC PROPERTIES ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF MATERIALS THEREFOR ; WOODSTAINS</subject><creationdate>1968</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=19680131&DB=EPODOC&CC=CH&NR=450718A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19680131&DB=EPODOC&CC=CH&NR=450718A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KOCH,GERHARD</creatorcontrib><creatorcontrib>BORNHAUPT,BERND,V</creatorcontrib><creatorcontrib>RATING,WILHELM,DR</creatorcontrib><title>Verfahren zur Herstellung von härtbaren, modifizierten Harzen auf der Grundlage von aromatischen Di- und/oder Polycarbonsäuren und Aminen</title><description>A process for making heat-hardenable polyesterimides comprises reacting 10 equivalents of an aromatic polycarboxylic acid with at least one pair of carboxyl groups in ortho position to each other with from 5 to 16 equivalents of di- and/or trihydric alcohols and from 5.5 0.5 equivalents of di-primary amines, amino acids and/or hydroxyamines, where for every 10 equivalents of difunctional compounds there are from 4 to 20, preferably from 6 to 15 equivalents of polyfunctional compounds, at temperatures of up to 250 DEG C., if desired in the presence of solvents and/or carriers, the reaction being continued until the product becomes clear. Dicarboxylic acids may be present in the reaction mixture. An ester of zirconic or titanic acid in an amount to provide 0.1 to 0.2 gram of titanium or zirconium for every 100 gram of the polyesterimide may be present in the reactants or may be reacted with the polyesterimide. The carboxylic acids may be wholly or partially replaced by their anhydrides or lower alkyl esters thereof. Specified carboxylic acids are trimellitic, pyromellitic and terephthalic acid. Specified polyols are ethylene glycol, diethylene glycol, 1: 2-propanediol, 2: 2-dimethyl-1: 3-propane diol, 4: 41-bis(hydroxyethoxy) diphenyl dimethyl methane, glycerine, trimethylol propane, trimethylol ethane and mixtures thereof. Specified amino compounds are phenylene diamine, 4: 41-diamino diphenyl, 4: 41-diamino diphenyl-methane, 4: 41-diamino dicyclohexyl-methane, 4: 41-diamino diphenyl ethers, diamino diphenyl sulphones, aminobenzoic acids, aminoethanol and amino phenols.</description><subject>ADHESIVES</subject><subject>BASIC ELECTRIC ELEMENTS</subject><subject>CABLES</subject><subject>CHEMICAL PAINT OR INK REMOVERS</subject><subject>CHEMISTRY</subject><subject>COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>CONDUCTORS</subject><subject>CORRECTING FLUIDS</subject><subject>DYES</subject><subject>ELECTRICITY</subject><subject>FILLING PASTES</subject><subject>INKS</subject><subject>INSULATORS</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</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>PASTES OR SOLIDS FOR COLOURING OR PRINTING</subject><subject>POLISHES</subject><subject>SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING ORDIELECTRIC PROPERTIES</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><subject>USE OF MATERIALS THEREFOR</subject><subject>WOODSTAINS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1968</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFjT0OgkAQRmksjHoFMweQqFGjLcEfSgtjS0YYYJNll8zumsgVvAY34WIuxt7qFe99-cbB-05cYMWkoHUMCbGxJKVTJTy1gqrv2D7Q6wXUOheFaAWx9XWC3HqgKyAnhgs7lUss6TtD1jVaYbLKJ0cRgpdLPXRXLV8Z8kMr03duuPUKolooUtNgVKA0NPtxEszPp1uchNTolEyDGSmyaZxsd6v9-hBt_gYf7g5NhQ</recordid><startdate>19680131</startdate><enddate>19680131</enddate><creator>KOCH,GERHARD</creator><creator>BORNHAUPT,BERND,V</creator><creator>RATING,WILHELM,DR</creator><scope>EVB</scope></search><sort><creationdate>19680131</creationdate><title>Verfahren zur Herstellung von härtbaren, modifizierten Harzen auf der Grundlage von aromatischen Di- und/oder Polycarbonsäuren und Aminen</title><author>KOCH,GERHARD ; BORNHAUPT,BERND,V ; RATING,WILHELM,DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CH450718A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1968</creationdate><topic>ADHESIVES</topic><topic>BASIC ELECTRIC ELEMENTS</topic><topic>CABLES</topic><topic>CHEMICAL PAINT OR INK REMOVERS</topic><topic>CHEMISTRY</topic><topic>COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>CONDUCTORS</topic><topic>CORRECTING FLUIDS</topic><topic>DYES</topic><topic>ELECTRICITY</topic><topic>FILLING PASTES</topic><topic>INKS</topic><topic>INSULATORS</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</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>PASTES OR SOLIDS FOR COLOURING OR PRINTING</topic><topic>POLISHES</topic><topic>SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING ORDIELECTRIC PROPERTIES</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><topic>USE OF MATERIALS THEREFOR</topic><topic>WOODSTAINS</topic><toplevel>online_resources</toplevel><creatorcontrib>KOCH,GERHARD</creatorcontrib><creatorcontrib>BORNHAUPT,BERND,V</creatorcontrib><creatorcontrib>RATING,WILHELM,DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KOCH,GERHARD</au><au>BORNHAUPT,BERND,V</au><au>RATING,WILHELM,DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung von härtbaren, modifizierten Harzen auf der Grundlage von aromatischen Di- und/oder Polycarbonsäuren und Aminen</title><date>1968-01-31</date><risdate>1968</risdate><abstract>A process for making heat-hardenable polyesterimides comprises reacting 10 equivalents of an aromatic polycarboxylic acid with at least one pair of carboxyl groups in ortho position to each other with from 5 to 16 equivalents of di- and/or trihydric alcohols and from 5.5 0.5 equivalents of di-primary amines, amino acids and/or hydroxyamines, where for every 10 equivalents of difunctional compounds there are from 4 to 20, preferably from 6 to 15 equivalents of polyfunctional compounds, at temperatures of up to 250 DEG C., if desired in the presence of solvents and/or carriers, the reaction being continued until the product becomes clear. Dicarboxylic acids may be present in the reaction mixture. An ester of zirconic or titanic acid in an amount to provide 0.1 to 0.2 gram of titanium or zirconium for every 100 gram of the polyesterimide may be present in the reactants or may be reacted with the polyesterimide. The carboxylic acids may be wholly or partially replaced by their anhydrides or lower alkyl esters thereof. Specified carboxylic acids are trimellitic, pyromellitic and terephthalic acid. Specified polyols are ethylene glycol, diethylene glycol, 1: 2-propanediol, 2: 2-dimethyl-1: 3-propane diol, 4: 41-bis(hydroxyethoxy) diphenyl dimethyl methane, glycerine, trimethylol propane, trimethylol ethane and mixtures thereof. Specified amino compounds are phenylene diamine, 4: 41-diamino diphenyl, 4: 41-diamino diphenyl-methane, 4: 41-diamino dicyclohexyl-methane, 4: 41-diamino diphenyl ethers, diamino diphenyl sulphones, aminobenzoic acids, aminoethanol and amino phenols.</abstract><edition>1</edition><oa>free_for_read</oa></addata></record> |
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subjects | ADHESIVES BASIC ELECTRIC ELEMENTS CABLES CHEMICAL PAINT OR INK REMOVERS CHEMISTRY COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS COMPOSITIONS BASED THEREON CONDUCTORS CORRECTING FLUIDS DYES ELECTRICITY FILLING PASTES INKS INSULATORS MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NATURAL RESINS ORGANIC MACROMOLECULAR COMPOUNDS PAINTS PASTES OR SOLIDS FOR COLOURING OR PRINTING POLISHES SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING ORDIELECTRIC PROPERTIES THEIR PREPARATION OR CHEMICAL WORKING-UP USE OF MATERIALS THEREFOR WOODSTAINS |
title | Verfahren zur Herstellung von härtbaren, modifizierten Harzen auf der Grundlage von aromatischen Di- und/oder Polycarbonsäuren und Aminen |
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