Michael-addition-hardening hybrid system for chemical fixing technology

US12180394B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12180394-B2
Application numberUS-202017780985-A
CountryUS
Kind codeB2
Filing dateDec 1, 2020
Priority dateDec 4, 2019
Publication dateDec 31, 2024
Grant dateDec 31, 2024

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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).

The invention claimed is: 1. A method for mortar-bonded fixing of anchoring elements in a hole or a crevice in a substrate, comprising introducing a hybrid system adhesive and an anchoring means one after the other or simultaneously or in a mixed form with partial introduction in each case, into a hole or crevice in a substrate, wherein the hybrid system includes as constituents 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 allowing the parallel reaction of constituents a), b) and c) to harden. 2. The method for mortar-bonded fixing of anchoring elements in holes or crevices according to claim 1 , comprising using a-introducing the hybrid system and an anchoring means one after the other or simultaneously into a hole or crevice in a substrate. 3. The method according to claim 2 , wherein the hybrid system is in the form of a two-component system. 4. The method according to claim 2 , wherein the hybrid system further includes a catalyst. 5. The method according to claim 2 wherein the hybrid system is used in the form of a two-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. 6. The method according to claim 2 , wherein, in the hybrid system, the reaction resin based on α,β-unsaturated compounds is a reaction resin-selected from the group consisting of hydroxy-C 2 -C 10 alkyl-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 polyethoxytriacrylate, 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 which are acid halides or active esters or from the reaction of polyester polyols with acrylic acid or reactive derivatives thereof as just mentioned, urethane acrylates obtainable by reaction of isocyanates with an OH-group-containing acrylate selected from the group consisting of hydroxyethyl-, hydroxypropyl-, hydroxybutyl-or pentaerythritol-tri-acrylate, and tetrafunctional polyester acrylates); an acrylic-functional alkoxysilane or organopolysiloxane selected from the group consisting of acrylatomethyl-trim ethoxysilane,-methyldimethoxysilane,-dimethylmethoxysilane,-triethoxysilane or -methyldiethoxysilane, acrylamidomethyl-trimethoxysilane,-methyldimethoxysilane,-dimethylmethoxysilane, -triethoxysilane, or-methyldiethoxysilane,-methyl-dimethylethoxysilane; a polyester resin based on maleic, fumaric or itaconic acid or a respective anhydride thereof; a polyester, polyurethane, polyether and/or alkyd resin that carries activated, ethylenically unsaturated groups; and an α,β-unsaturated compound having biogenic content having biogenic acrylate content of hydroxy-group-containing vegetable oils, selected from the group consisting of castor oil or soybean oil, a wholly or at least partly biogenic C1-C10) alkan (mono-, di-, tri-, tetra-, penta-or hexa-or poly-) ol acrylate, a partly or wholly biogenic polyglycerol acrylate, a wholly or partly biogenic acrylate of one or more sugar alcohols selected from the group consisting of mannitol, xylitol and sorbitol, a wholly or partly biogenic acrylated fusel oil, a wholly or partly biogenic 5-or 6-membered-ring heterocyclyl acrylate having one or two hetero atoms selected from O, N and S in the ring, or a partly or wholly biogenic glycerol or polyglycerol acrylate, and 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; the reaction resin based on compounds that include one or more CH-acidic methylene groups is one comprising malonic acid or a malonic acid ester, cyanoacetic acid esters, an acetoacetate, an acetoacetate-group-carrying oligomer or polymer which is obtainable, by transesterification of acetoacetic acid esters, an acetoacetate-group-carrying oligomer or polymer which is obtainable by copolymerisation of acetoacetoxyethyl methacrylate, an oligomer or polymer which is obtainable from dialkyl malonates and diols, or an acetoacetylated novolak, or a mixture of two or more thereof; the primary amine is selected from the group consisting of 1,2-diaminoethane, 2-methylpentanediamine, 2,2-dimethyl-1,3-propanediamine, 2,2,4-or 2,4,4-trimethylhexamethylenediamine, 1,13-diamino-4, 7, 10-trioxatridecane, commercially available amine-functionalised polyoxyalkylenes, triethylenetetramine, isophoronediamine, 1,3-and/or 1,4-bisaminomethylcyclohexane, TCD-diamine, 1,2-or 1,4-diaminocyclohexane, bis (4-aminocyclohexyl) methane, bis (4-amino-3-methylcyclohexyl) methane, norbornanediamine, diaminodicyclohexylmethane, 2,2-bis (4-aminocyclohexyl)propane, aminoethylpiperazine, 1,3-or 1,4-benzenedimethanamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, 1,3-benzenedimethanamine, 1,4-benzenedimethanamine, 1,6-diamino-2,2,4-trimethylhexane, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, N-aminoethylpiperazine, 1,3-bis (aminomethyl) cyclohexane, TCD-diamine, Jeffamines, dipropylenetriamine, N,N′-dicyclohexyl-1,6-hexanediamine, N,N′-dimethyl-1,3-diaminopropane, N,N′-diethyl-1,3-diaminopropane, N,N-dimethyl-1,3-diaminopropane, secondary polyoxypropylene-di-and-tri-amines, 2,5-diamino-2,5-dimethylhexane, bis (aminomethyl) tricyclopentadiene, 1,8-diamino-p-menthane and bis (4-amino-3, 5-dimethylcyclohexyl)methane, an aminoalkylsilane that includes at least one hydrolysable alkoxy group selected from the group consisting of one or more of the following compo

Assignees

Inventors

Classifications

  • characterised by the composition of the setting material or mixture (F16B13/143 takes precedence) · CPC title

  • C09D179/02Primary

    Polyamines · CPC title

  • 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

  • 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

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What does patent US12180394B2 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 Tue Dec 31 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).