Michael-addition-hardening hybrid system for chemical fixing technology

US2023002653A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2023002653-A1
Application numberUS-202017780985-A
CountryUS
Kind codeA1
Filing dateDec 1, 2020
Priority dateDec 4, 2019
Publication dateJan 5, 2023
Grant date

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  5. First independent claim

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Abstract

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A hybrid system for use as an adhesive, coating or paint, wherein the hybrid system includes a) a reaction resin based on α,β-unsaturated compounds, b) a reaction resin based on compounds that include CH-acidic methylene groups, and c) a primary amine, and to related subject matter.

First claim

Opening claim text (preview).

1 . A hybrid system for use as an adhesive, coating or paint, characterised in that the hybrid system includes a) a reaction resin based on α,β-unsaturated compounds, b) a reaction resin based on compounds that include CH-acidic methylene groups, and c) a primary amine. 2 . The hybrid system according to claim 1 as an adhesive for chemical fixing technology, especially for fixing anchoring means in drilled holes, which system includes a reaction resin based on α,β-unsaturated compounds, a reaction resin based on compounds that include CH-acidic methylene groups, and a primary amine. 3 . The hybrid system according to claim 1 in the form of a multi-component system, especially a two-component system. 4 . The hybrid system according to claim 1 in the form of a two-component kit. 5 . The hybrid system according to claim 1 , further including a catalyst. 6 . The hybrid system according to claim 1 in the form of a multi-component kit, wherein (i) constituents a) and b) are present in one component, while constituent c) is present together with a catalyst in a different component which is not capable of mixing in the stored state, it being optionally possible in each case for one or more further ingredients to be present; or (ii) constituents a), b) and the epoxy moiety of an epoxy/tert-amine catalyst are present in one component, and constituent c) is present together with the tert-amine moiety of an epoxy/tert-amine catalyst in a different component, it being optionally possible in each case for one or more further additional ingredients to be present. 7 . The hybrid system according to claim 1 , wherein the reaction resin based on α,β-unsaturated compounds is a reaction resin which comprises or consists of an α,β-unsaturated compound that carries at least one fumarate, maleate, itaconate or acrylate group or preferably two or more thereof, such as an acrylic acid ester or acrylamide, for example a mono- or especially di-, tri-, tetra- or higher polyacrylate, especially selected from hydroxy-C 2 -C 10 alkyl-acrylate, such as hydroxyethyl, hydroxypropyl or hydroxybutyl acrylate, ethanediol diacrylate, 1,3-propanediol diacrylate, 1,4-butanediol acrylate, poly(butanediol) diacrylate, polybutadiene diacrylate, 3-methyl-1,5-pentanediol -diacrylate, 1,6-hexanediol diacrylate, diethyleneglycol diacrylate, tetraethyleneglycol diacrylate, tripropyleneglycol diacrylate, triethyleneglycol diacrylate, triisopropyleneglycol diacrylate, dipropyleneglycol diacrylate, neopentylglycol diacrylate, ethoxylated or propoxylated neopentylglycol diacrylate, tripropyleneglycol diacrylate, bisphenol-A-, bisphenol-F-, bisphenol-AF- or bisphenol-S-diglycidyl ether diacrylate, bisphenol-A-polyethoxydiacrylates, bisphenol-F-polyethoxydiacrylates, polyethyleneglycol diacrylates, polypropyleneglycol diacrylates, trimethylolpropane triacrylate, di-trimethylolpropane tetraacrylate, trimethylolpropane polyethoxy-triacrylate, ethoxylated or propoxylated trimethylolpropane triacrylate, glycerol triacrylate, ethoxylated or propoxylated glycerol triacrylate, tris(2-acryloxyethyl) isocyanurate, pentaerythritol triacrylate, pentaerythritol monohydroxytriacrylate, pentaerythritol triethoxytriacrylate, pentaerythritol tetraacrylate, ethoxylated or propoxylated pentaerythritol tetraacrylate, ditrimethylolpropane tetraacrylate, dipentaerythritol pentaacrylate, dipentaerythritol polyhexanolide hexaacrylate, dipentaerythritol hexaacrylate, tris(hydroxyethyl)isocyanuratopolyhexanolide triacrylate, tris(2-hydroxyethyl)isocyanuratotriacrylate, tricyclodecanedimethylol diacrylate, esterdiol diacrylate, 2-(2-acryloyloxy-1,1-dimethyl)-5-ethyl-5-acryloyloxymethyl-1,3-dioxane, tetrabromobisphenol-A-diethoxydiacrylate, 4,4-dimercaptodiphenylsulfide diacrylate, polytetraethyleneglycol diacrylate, 1,9-nonanediol diacrylate, 1,10-decanediol diacrylate, dimethylolpropane tetraacrylate, cresol epoxyacrylates, novolak “poly”acrylate, acrylate-group-containing oligomers or polymers from the reaction of polyepoxides with acrylic acid or reactive derivatives thereof, such as acid halides or active esters or from the reaction of polyester polyols with acrylic acid or reactive derivatives thereof, especially as just mentioned, or urethane acrylates (obtainable, for example, by reaction of isocyanates with an OH-group-containing acrylate, such as hydroxyethyl-, hydroxypropyl-, hydroxybutyl- or pentaerythritol-tri-acrylate, and polyester acrylate resins, for example tetrafunctional polyester acrylates); an acrylic-functional alkoxysilane or organopolysiloxane, such as acrylatomethyl-trimethoxysilane, -methyldimethoxy-silane, -dimethylmethoxysilane, -triethoxysilane or -methyldiethoxysilane, acrylamido-methyl-trimethoxysilane, -methyldimethoxysilane, -dimethylmethoxysilane, -triethoxy-silane, or -methyldiethoxysilane, -methyl-dimethylethoxysilane; or a polyester resin based on maleic, fumaric or itaconic acid or a respective anhydride thereof; or a polyester, polyurethane, polyether and/or alkyd resin that carries activated, ethylenically unsaturated groups; or an α,β-unsaturated compound having biogenic content, especially an acrylate, preferably having biogenic acrylate content of hydroxy-group-containing vegetable oils, such as of castor oil or soybean oil, a wholly or at least partly biogenic (for example C 1 -C 10 )alkan(mono-, preferably di-, tri-, tetra-, penta- or hexa- or poly-)ol acrylate, a partly or preferably wholly biogenic polyglycerol acrylate, a wholly or partly biogenic acrylate of one or more sugar alcohols, such as mannitol, xylitol or sorbitol, a wholly or partly biogenic acrylated fusel oil, a wholly or partly biogenic 5- or 6-membered-ring heterocyclyl acrylate (especially having one or two hetero atoms selected from O, N and S in the ring), or a partly or preferably wholly biogenic glycerol or polyglycerol acrylate, or a wholly or partly biogenic saccharide acrylate; or the corresponding methacrylates; or a mixture of two or more of the mentioned α,β-unsaturated compounds. 8 . The hybrid system according to claim 1 , wherein the reaction resin that carries one or more CH-acidic methylene groups is one comprising malonic acid or a malonic acid ester, such as malonic acid dimethyl ester, malonic acid diethyl ester, malonic acid di-n-propyl ester, malonic acid diisopropyl ester, malonic acid dibutyl ester, malonic acid di-(2-ethylhexyl) ester or malonic acid dilauryl ester, cyanoacetic acid esters, such as 2-ethylhexyl cyanoacetate, butyl cyanoacetate, octyl cyanoacetate, 2-methoxyethyl cyanoacetate, a dione, such as pentane-2,4-dione, hexane-2,4-dione, heptane-2,4-dione, 1-methoxy-2,4-pentanedione, 1-phenyl-1,3-butanedione, 1,3-diphenyl-1,3-propanedione, 4,6-dioxoheptanoic acid methyl ester, 5,7-dioxooctanoic acid methyl ester, an acetoacetate, such as benzoylacetoacetic acid methyl, ethyl or butyl ester, propionylacetic acid methyl, ethyl or butyl ester, butyroylacetic acid methyl ester, acetoacetic acid methyl, ethyl, isopropyl, n-butyl, isobutyl or tert-butyl ester, acetoacetic acid (2-methoxyethyl) ester, acetoacetic acid (2-ethylhexyl) ester, acetoacetic acid lauryl ester, 2-acetoacetatoethyl acrylate, acetoacetic acid benzyl ester, 1,4-butanediol diacetoacetate, 1,6-hexanediol diacetoacetate, neopentyl glycol diacetoacetate, 2-ethyl-2-butyl-1, 3-propanediol diacetoacetate, cyclohexanedimethanol diacetoacetate, free or ethoxylated bisphenol-A-, -F-, -AF- or -S-diacetoacetate, trimethylolpropane triacetoacetate, pentaerythritol tri- or tetra-acetoacetate, ditrimethylolpropane tetraacetoacetate, di pentaerythritol hexaacetoacetate, an acetoacetate-group-carrying oligomer or polymer which is obtainable, for example, by transesterification of acetoacetic acid (for example ethyl) esters, an acetoacetate-group-carrying olig

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Inventors

Classifications

  • Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain (C08L7/00 - C08L57/00, C08L61/00 take precedence); Compositions of derivatives of such polymers · CPC title

  • Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes · CPC title

  • C09D179/02Primary

    Polyamines · CPC title

  • Adhesives based on macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain (C09J107/00 - C09J157/00, C09J161/00 take precedence); Adhesives based on derivatives of such polymers · CPC title

  • Polyalkylene(poly)amines · CPC title

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What does patent US2023002653A1 cover?
A hybrid system for use as an adhesive, coating or paint, wherein the hybrid system includes a) a reaction resin based on α,β-unsaturated compounds, b) a reaction resin based on compounds that include CH-acidic methylene groups, and c) a primary amine, and to related subject matter.
Who is the assignee on this patent?
Fischerwerke Gmbh & Co Kg
What technology area does this patent fall under?
Primary CPC classification C09D179/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).