Blokerede polyurethanpræpolymerer som klæbestoffer
Reactive systems (A) comprises one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate (B1), a polyol component (B2) and CH azide cyclic ketone (I)); one or more OH-functionalized compounds (A2); and optionally catalysts (A3) an...
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creator | GUERTLER, CHRISTOPH SCHELHAAS, MICHAEL WINTERMANTEL, MATTHIAS TRINKS, RAINER MECKEL, WALTER |
description | Reactive systems (A) comprises one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate (B1), a polyol component (B2) and CH azide cyclic ketone (I)); one or more OH-functionalized compounds (A2); and optionally catalysts (A3) and further additives (A4). Reactive systems (A) comprises: one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate with a free isocyanate (NCO) groups of 5-60 wt.%) (B1), a polyol component (B2) (containing at least a polyester polyol, a polyetherpolyol and/or a polycarbonate polyol) and CH azide cyclic ketone of formula (I) (where n is a blocking agent), where the isocyanate group containing blocked NCO groups of 0.1-20 wt.%; one or more OH-functionalized compounds (A2) (where the OH component is activated by beta -end amine component); and optionally catalysts (A3) and further additives (A4). X : electron with drawing group; R 1>, R 2>H, 1-20C (cyclo)alkyl, 6-24C aryl, 1-20C (cyclo)alkyl ester, 6-24C arylester or amide, mixed 1-24C aliphatic/aromatic residues (which can be also part 4-8 linear ring); and n : 0-5. Independent claims are also included for: (1) the preparation of (A); (2) preparation of composite systems, comprises coating either one- or both sides of the joining parts with (A); and (3) composite systems obtained by the method. [Image]. |
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Reactive systems (A) comprises: one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate with a free isocyanate (NCO) groups of 5-60 wt.%) (B1), a polyol component (B2) (containing at least a polyester polyol, a polyetherpolyol and/or a polycarbonate polyol) and CH azide cyclic ketone of formula (I) (where n is a blocking agent), where the isocyanate group containing blocked NCO groups of 0.1-20 wt.%; one or more OH-functionalized compounds (A2) (where the OH component is activated by beta -end amine component); and optionally catalysts (A3) and further additives (A4). X : electron with drawing group; R 1>, R 2>H, 1-20C (cyclo)alkyl, 6-24C aryl, 1-20C (cyclo)alkyl ester, 6-24C arylester or amide, mixed 1-24C aliphatic/aromatic residues (which can be also part 4-8 linear ring); and n : 0-5. Independent claims are also included for: (1) the preparation of (A); (2) preparation of composite systems, comprises coating either one- or both sides of the joining parts with (A); and (3) composite systems obtained by the method. [Image].</description><language>dan</language><subject>ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE ; ADHESIVES ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; DYES ; 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 MACROMOLECULAR COMPOUNDS ; PAINTS ; POLISHES ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF MATERIALS AS ADHESIVES</subject><creationdate>2007</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=20070827&DB=EPODOC&CC=DK&NR=1634904T3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25551,76302</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20070827&DB=EPODOC&CC=DK&NR=1634904T3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>GUERTLER, CHRISTOPH</creatorcontrib><creatorcontrib>SCHELHAAS, MICHAEL</creatorcontrib><creatorcontrib>WINTERMANTEL, MATTHIAS</creatorcontrib><creatorcontrib>TRINKS, RAINER</creatorcontrib><creatorcontrib>MECKEL, WALTER</creatorcontrib><title>Blokerede polyurethanpræpolymerer som klæbestoffer</title><description>Reactive systems (A) comprises one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate (B1), a polyol component (B2) and CH azide cyclic ketone (I)); one or more OH-functionalized compounds (A2); and optionally catalysts (A3) and further additives (A4). Reactive systems (A) comprises: one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate with a free isocyanate (NCO) groups of 5-60 wt.%) (B1), a polyol component (B2) (containing at least a polyester polyol, a polyetherpolyol and/or a polycarbonate polyol) and CH azide cyclic ketone of formula (I) (where n is a blocking agent), where the isocyanate group containing blocked NCO groups of 0.1-20 wt.%; one or more OH-functionalized compounds (A2) (where the OH component is activated by beta -end amine component); and optionally catalysts (A3) and further additives (A4). X : electron with drawing group; R 1>, R 2>H, 1-20C (cyclo)alkyl, 6-24C aryl, 1-20C (cyclo)alkyl ester, 6-24C arylester or amide, mixed 1-24C aliphatic/aromatic residues (which can be also part 4-8 linear ring); and n : 0-5. Independent claims are also included for: (1) the preparation of (A); (2) preparation of composite systems, comprises coating either one- or both sides of the joining parts with (A); and (3) composite systems obtained by the method. 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Reactive systems (A) comprises: one or more blocked polyurethane prepolymer (A1) (based on aromatic, aliphatic, araliphatic and/or cyclo-aliphatic diisocyanate with a free isocyanate (NCO) groups of 5-60 wt.%) (B1), a polyol component (B2) (containing at least a polyester polyol, a polyetherpolyol and/or a polycarbonate polyol) and CH azide cyclic ketone of formula (I) (where n is a blocking agent), where the isocyanate group containing blocked NCO groups of 0.1-20 wt.%; one or more OH-functionalized compounds (A2) (where the OH component is activated by beta -end amine component); and optionally catalysts (A3) and further additives (A4). X : electron with drawing group; R 1>, R 2>H, 1-20C (cyclo)alkyl, 6-24C aryl, 1-20C (cyclo)alkyl ester, 6-24C arylester or amide, mixed 1-24C aliphatic/aromatic residues (which can be also part 4-8 linear ring); and n : 0-5. Independent claims are also included for: (1) the preparation of (A); (2) preparation of composite systems, comprises coating either one- or both sides of the joining parts with (A); and (3) composite systems obtained by the method. [Image].</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE ADHESIVES CHEMISTRY COMPOSITIONS BASED THEREON DYES 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 MACROMOLECULAR COMPOUNDS PAINTS POLISHES THEIR PREPARATION OR CHEMICAL WORKING-UP USE OF MATERIALS AS ADHESIVES |
title | Blokerede polyurethanpræpolymerer som klæbestoffer |
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