Adhesive composition containing polyepoxide materials

An adhesive composition contains a glycidyl polyether of a dihydric phenol having a Durrans' mercury melting-point below 30 DEG C. and a 1,2-epoxy equivalency of 1.6-2.0 with 3-20 per cent of a second glycidyl polyether of a dihydric phenol with a melting-point above 75 DEG C. and an epoxy equi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
1. Verfasser: NAPS MARGUERITE
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator NAPS MARGUERITE
description An adhesive composition contains a glycidyl polyether of a dihydric phenol having a Durrans' mercury melting-point below 30 DEG C. and a 1,2-epoxy equivalency of 1.6-2.0 with 3-20 per cent of a second glycidyl polyether of a dihydric phenol with a melting-point above 75 DEG C. and an epoxy equivalence of 1.2-1.8. The first polyether contains 1-1.5 aromatic radicals and the second at least 4. A liquid aliphatic polyepoxide, e.g. bis-(2,3-epoxypropyl) ether or thioether; 1,2-bis-(2,3-epoxypropyloxy) ethane; glycidyl ethers of polyhydric alcohols such as glycerol, diethylene glycol, pentaerythritol or polyally alcohol; or epoxidized drying oils as described in U.S.A. Specification 2,485,160, may also be present. The polyethers are prepared by heating epichlorohydrin or glyceryl dichlorohydrin with resorcinol, 1,1-bis (4-hydroxyphenyl) ethane, propane, butane or 2-ethylhexane, 2,2-bis (4-hydroxyphenyl) propane or butane, 3,3-bis (4-hydroxyphenyl) pentane or the isomeric 2,41-and 2,21 dihydroxy phenyl compounds, and with sodium hydroxide. The two polyethers may be prepared from the same or different phenols. The higher molecular weight polyether may be made by reacting a lower molecular weight one with more polyhydric phenol. Preferably the powdered high-melting polyether is dissolved in the molten low-melting one, and the liquid aliphatic polyepoxide added if desired for thinning. Nitriles, e.g. aceto-, propio-, butyro-, capro-, lauro-, acrylo-, methacrylo-, croto-, oleo-, succino-, glutaro-, adipo-, or fumaro-, may also be added to reduce the viscosity of the mixture. Fillers which may be added are asbestos, aluminium oxide, iron oxide, silica, bauxite, zinc oxide, china clay, titanium oxide and silicon carbide. Suitable hardening agents are alkaline, e.g. sodium hydroxide or phenoxide, acids, e.g. formic, oxalic, phthalic, phosphoric or partial phosphates, e.g. diethyl orthophosphate, hexaethyl tetraphosphate, Friedel-Crafts' catalysts or complexes thereof, and amino compounds, e.g. triethylamine, ethylene diamine, pyridine, N,N-diethyl - 1,3 - propanediamine, dicyandiamide, melamine or others. The preparation of a number of specific polyethers is described, together with the preparation of compositions containing them and the use of those compositions as adhesives particularly for joining metals.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_US2682515A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>US2682515A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_US2682515A3</originalsourceid><addsrcrecordid>eNrjZDB1TMlILc4sS1VIzs8tyC_OLMnMzwOy80oSM_My89IVCvJzKlML8isyU1IVchNLUosyE3OKeRhY04BUKi-U5maQd3MNcfbQBaqMTy0uSExOzUstiQ8NNjKzMDI1NHU0JqwCACKtLXs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Adhesive composition containing polyepoxide materials</title><source>esp@cenet</source><creator>NAPS MARGUERITE</creator><creatorcontrib>NAPS MARGUERITE</creatorcontrib><description>An adhesive composition contains a glycidyl polyether of a dihydric phenol having a Durrans' mercury melting-point below 30 DEG C. and a 1,2-epoxy equivalency of 1.6-2.0 with 3-20 per cent of a second glycidyl polyether of a dihydric phenol with a melting-point above 75 DEG C. and an epoxy equivalence of 1.2-1.8. The first polyether contains 1-1.5 aromatic radicals and the second at least 4. A liquid aliphatic polyepoxide, e.g. bis-(2,3-epoxypropyl) ether or thioether; 1,2-bis-(2,3-epoxypropyloxy) ethane; glycidyl ethers of polyhydric alcohols such as glycerol, diethylene glycol, pentaerythritol or polyally alcohol; or epoxidized drying oils as described in U.S.A. Specification 2,485,160, may also be present. The polyethers are prepared by heating epichlorohydrin or glyceryl dichlorohydrin with resorcinol, 1,1-bis (4-hydroxyphenyl) ethane, propane, butane or 2-ethylhexane, 2,2-bis (4-hydroxyphenyl) propane or butane, 3,3-bis (4-hydroxyphenyl) pentane or the isomeric 2,41-and 2,21 dihydroxy phenyl compounds, and with sodium hydroxide. The two polyethers may be prepared from the same or different phenols. The higher molecular weight polyether may be made by reacting a lower molecular weight one with more polyhydric phenol. Preferably the powdered high-melting polyether is dissolved in the molten low-melting one, and the liquid aliphatic polyepoxide added if desired for thinning. Nitriles, e.g. aceto-, propio-, butyro-, capro-, lauro-, acrylo-, methacrylo-, croto-, oleo-, succino-, glutaro-, adipo-, or fumaro-, may also be added to reduce the viscosity of the mixture. Fillers which may be added are asbestos, aluminium oxide, iron oxide, silica, bauxite, zinc oxide, china clay, titanium oxide and silicon carbide. Suitable hardening agents are alkaline, e.g. sodium hydroxide or phenoxide, acids, e.g. formic, oxalic, phthalic, phosphoric or partial phosphates, e.g. diethyl orthophosphate, hexaethyl tetraphosphate, Friedel-Crafts' catalysts or complexes thereof, and amino compounds, e.g. triethylamine, ethylene diamine, pyridine, N,N-diethyl - 1,3 - propanediamine, dicyandiamide, melamine or others. The preparation of a number of specific polyethers is described, together with the preparation of compositions containing them and the use of those compositions as adhesives particularly for joining metals.</description><language>eng</language><subject>ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE ; ADHESIVES ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; DYES ; HETEROCYCLIC COMPOUNDS ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; PAINTS ; POLISHES ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF MATERIALS AS ADHESIVES</subject><creationdate>1954</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&amp;date=19540629&amp;DB=EPODOC&amp;CC=US&amp;NR=2682515A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19540629&amp;DB=EPODOC&amp;CC=US&amp;NR=2682515A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAPS MARGUERITE</creatorcontrib><title>Adhesive composition containing polyepoxide materials</title><description>An adhesive composition contains a glycidyl polyether of a dihydric phenol having a Durrans' mercury melting-point below 30 DEG C. and a 1,2-epoxy equivalency of 1.6-2.0 with 3-20 per cent of a second glycidyl polyether of a dihydric phenol with a melting-point above 75 DEG C. and an epoxy equivalence of 1.2-1.8. The first polyether contains 1-1.5 aromatic radicals and the second at least 4. A liquid aliphatic polyepoxide, e.g. bis-(2,3-epoxypropyl) ether or thioether; 1,2-bis-(2,3-epoxypropyloxy) ethane; glycidyl ethers of polyhydric alcohols such as glycerol, diethylene glycol, pentaerythritol or polyally alcohol; or epoxidized drying oils as described in U.S.A. Specification 2,485,160, may also be present. The polyethers are prepared by heating epichlorohydrin or glyceryl dichlorohydrin with resorcinol, 1,1-bis (4-hydroxyphenyl) ethane, propane, butane or 2-ethylhexane, 2,2-bis (4-hydroxyphenyl) propane or butane, 3,3-bis (4-hydroxyphenyl) pentane or the isomeric 2,41-and 2,21 dihydroxy phenyl compounds, and with sodium hydroxide. The two polyethers may be prepared from the same or different phenols. The higher molecular weight polyether may be made by reacting a lower molecular weight one with more polyhydric phenol. Preferably the powdered high-melting polyether is dissolved in the molten low-melting one, and the liquid aliphatic polyepoxide added if desired for thinning. Nitriles, e.g. aceto-, propio-, butyro-, capro-, lauro-, acrylo-, methacrylo-, croto-, oleo-, succino-, glutaro-, adipo-, or fumaro-, may also be added to reduce the viscosity of the mixture. Fillers which may be added are asbestos, aluminium oxide, iron oxide, silica, bauxite, zinc oxide, china clay, titanium oxide and silicon carbide. Suitable hardening agents are alkaline, e.g. sodium hydroxide or phenoxide, acids, e.g. formic, oxalic, phthalic, phosphoric or partial phosphates, e.g. diethyl orthophosphate, hexaethyl tetraphosphate, Friedel-Crafts' catalysts or complexes thereof, and amino compounds, e.g. triethylamine, ethylene diamine, pyridine, N,N-diethyl - 1,3 - propanediamine, dicyandiamide, melamine or others. The preparation of a number of specific polyethers is described, together with the preparation of compositions containing them and the use of those compositions as adhesives particularly for joining metals.</description><subject>ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE</subject><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>DYES</subject><subject>HETEROCYCLIC COMPOUNDS</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>NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>PAINTS</subject><subject>POLISHES</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><subject>USE OF MATERIALS AS ADHESIVES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1954</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDB1TMlILc4sS1VIzs8tyC_OLMnMzwOy80oSM_My89IVCvJzKlML8isyU1IVchNLUosyE3OKeRhY04BUKi-U5maQd3MNcfbQBaqMTy0uSExOzUstiQ8NNjKzMDI1NHU0JqwCACKtLXs</recordid><startdate>19540629</startdate><enddate>19540629</enddate><creator>NAPS MARGUERITE</creator><scope>EVB</scope></search><sort><creationdate>19540629</creationdate><title>Adhesive composition containing polyepoxide materials</title><author>NAPS MARGUERITE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US2682515A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1954</creationdate><topic>ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE</topic><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>DYES</topic><topic>HETEROCYCLIC COMPOUNDS</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>NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>PAINTS</topic><topic>POLISHES</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><topic>USE OF MATERIALS AS ADHESIVES</topic><toplevel>online_resources</toplevel><creatorcontrib>NAPS MARGUERITE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAPS MARGUERITE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Adhesive composition containing polyepoxide materials</title><date>1954-06-29</date><risdate>1954</risdate><abstract>An adhesive composition contains a glycidyl polyether of a dihydric phenol having a Durrans' mercury melting-point below 30 DEG C. and a 1,2-epoxy equivalency of 1.6-2.0 with 3-20 per cent of a second glycidyl polyether of a dihydric phenol with a melting-point above 75 DEG C. and an epoxy equivalence of 1.2-1.8. The first polyether contains 1-1.5 aromatic radicals and the second at least 4. A liquid aliphatic polyepoxide, e.g. bis-(2,3-epoxypropyl) ether or thioether; 1,2-bis-(2,3-epoxypropyloxy) ethane; glycidyl ethers of polyhydric alcohols such as glycerol, diethylene glycol, pentaerythritol or polyally alcohol; or epoxidized drying oils as described in U.S.A. Specification 2,485,160, may also be present. The polyethers are prepared by heating epichlorohydrin or glyceryl dichlorohydrin with resorcinol, 1,1-bis (4-hydroxyphenyl) ethane, propane, butane or 2-ethylhexane, 2,2-bis (4-hydroxyphenyl) propane or butane, 3,3-bis (4-hydroxyphenyl) pentane or the isomeric 2,41-and 2,21 dihydroxy phenyl compounds, and with sodium hydroxide. The two polyethers may be prepared from the same or different phenols. The higher molecular weight polyether may be made by reacting a lower molecular weight one with more polyhydric phenol. Preferably the powdered high-melting polyether is dissolved in the molten low-melting one, and the liquid aliphatic polyepoxide added if desired for thinning. Nitriles, e.g. aceto-, propio-, butyro-, capro-, lauro-, acrylo-, methacrylo-, croto-, oleo-, succino-, glutaro-, adipo-, or fumaro-, may also be added to reduce the viscosity of the mixture. Fillers which may be added are asbestos, aluminium oxide, iron oxide, silica, bauxite, zinc oxide, china clay, titanium oxide and silicon carbide. Suitable hardening agents are alkaline, e.g. sodium hydroxide or phenoxide, acids, e.g. formic, oxalic, phthalic, phosphoric or partial phosphates, e.g. diethyl orthophosphate, hexaethyl tetraphosphate, Friedel-Crafts' catalysts or complexes thereof, and amino compounds, e.g. triethylamine, ethylene diamine, pyridine, N,N-diethyl - 1,3 - propanediamine, dicyandiamide, melamine or others. The preparation of a number of specific polyethers is described, together with the preparation of compositions containing them and the use of those compositions as adhesives particularly for joining metals.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_US2682515A
source esp@cenet
subjects ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE
ADHESIVES
CHEMISTRY
COMPOSITIONS BASED THEREON
DYES
HETEROCYCLIC COMPOUNDS
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
NATURAL RESINS
NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
PAINTS
POLISHES
THEIR PREPARATION OR CHEMICAL WORKING-UP
USE OF MATERIALS AS ADHESIVES
title Adhesive composition containing polyepoxide materials
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T11%3A59%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=NAPS%20MARGUERITE&rft.date=1954-06-29&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EUS2682515A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true