ADHESIVE COMPOSITIONS CONTAINING BLOCKED POLYURETHANE PREPOLYMERS

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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Hauptverfasser: MATTHIAS WINTERMANTEL, WALTER MECKEL, MICHAEL SCHELHAAS, CHRISTOPH GUERTLER, RAINER TRINKS
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creator MATTHIAS WINTERMANTEL
WALTER MECKEL
MICHAEL SCHELHAAS
CHRISTOPH GUERTLER
RAINER TRINKS
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&gt;, R 2&gt;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&gt;, R 2&gt;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. 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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&gt;, R 2&gt;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
COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
DYES
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 ADHESIVE COMPOSITIONS CONTAINING BLOCKED POLYURETHANE PREPOLYMERS
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