Aldimines and ketimines as initiators in hardener systems and corresponding resin compositions inter alia for fixing technology

US10544235B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10544235-B2
Application numberUS-201615738092-A
CountryUS
Kind codeB2
Filing dateJun 3, 2016
Priority dateJun 26, 2015
Publication dateJan 28, 2020
Grant dateJan 28, 2020

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A hardener system for a synthetic resin composition having free-radical-polymerisable compounds, which includes the following constituents: a) at least one activator in the form of a metal salt, and as free-radical starter b1) (i) at least one aldehyde and/or ketone and at least one primary amine, and/or b2) (ii) at least one aldimine or (iii) at least one ketimine, or a mixture of two or more of constituents (i) to (iii). In addition, synthetic resin compositions having such a hardener system for application especially in fixing technology, and subject matters related thereto.

First claim

Opening claim text (preview).

The invention claimed is: 1. A hardener system for a synthetic resin composition which includes free-radical-polymerisable compounds, comprising: at least one activator in the form of a metal salt; and, with no addition of other initiators, as initiator a free-radical starter comprising one or both of: (b1) at least one aldehyde and/or ketone which has at least one or more primary and/or secondary hydrogen atoms at the carbon atom in the α-position to the carbonyl group and at least one primary amine; and (b2) an imine obtained by reaction of at least one aldehyde and/or ketone which has at least one or more primary and/or secondary hydrogen atoms at the carbon atom in the α-position to the carbonyl group with at least one primary amine, which imine includes one or more imine structural increments of the formula (I): wherein independently of one another: the wavy line represents an organic radical of an amine, or hydrogen; and R 2 and R 3 each independently of the other denotes hydrogen or an unsubstituted or substituted organic radical which includes at least one aliphatic, heteroaliphatic, alicyclic or heterocyclic molecular structure, or a salt thereof. 2. The hardener system according to claim 1 , wherein: the at least one activator in the form of a metal salt comprises one or more salts of organic and/or inorganic acid with one or more metals, the one or more metals comprising one or more of copper, iron, vanadium, manganese, cerium, cobalt, zirconium, and bismuth; the inorganic acid comprising one or more of a sulfate radical and a carbonate radical; and the organic acid comprising a carboxylate radical; and the free-radical starter comprises (b2) the imine which includes one or more imine structural increments of the formula (I), the imine comprising at least one aldimine or ketimine, obtained by condensation, with removal of water, of a mono-, di- or poly-amine with one or more aldehydes or ketones, wherein: the mono-, di- or poly-amine comprises one or more of aminol; alkyl/alkylene(mono- or di-)amine; cycloalkyl/cycloalkylene(mono- or di-)amine; heterocycloalkyl/heterocycloalkylene(mono- or di-)amine; a compound of the formula H 2 N—(CH 2 ) i —NH—[(CH 2 ) j —NH] k —(CH 2 ) l —NH 2 , wherein i, j and l each independently of the others denotes from 2 to 4 and k denotes 0, 1, 2, 3 or 4; aminoamide; polyaminoamide; Mannich base; amine adduct; and aminoalkylsilane that includes at least one hydrolysable group; and the one or more aldehydes or ketones are of the formula (II), wherein: R 2 , R 3 each independently of the other denotes hydrogen or an unsubstituted or substituted organic radical which includes at least one aliphatic, heteroaliphatic, alicyclic, or heterocyclic molecular structure; and the one or more aldehydes and/or ketones are compounds which have at least one or more primary and/or secondary hydrogen atoms at the carbon atom in the α-position to the carbonyl group. 3. The hardener system according to claim 1 , wherein (b2) the imine which includes one or more imine structural increments of the formula (I) includes one or more aldimines and no ketimine. 4. The hardener system according to claim 1 , wherein: the activator in the form of a metal salt comprises one or more salts of organic and/or inorganic acids with metals, the one or more metals comprising one or more of copper, iron, vanadium, manganese, cerium, cobalt, zirconium, and bismuth; the inorganic acid comprising one or more of a sulfate radical and a carbonate radical; and the organic acid comprising a carboxylate radical; and the free-radical starter comprises (b2) the imine which includes one or more imine structural increments of the formula (I), the imine comprising at least one aldimine or ketimine, obtained by condensation, with removal of water, of a mono-, di- or poly-amine with one or more aldehydes or ketones, wherein: the mono-, di- or poly-amine comprises one or more of aminol; alkyl/alkylene(mono- or di-)amine; cycloalkyl/cycloalkylene(mono- or di-)amine; heterocycloalkyl/heterocycloalkylene(mono- or di-)amine; a compound of the formula H 2 N—(CH 2 ) i —NH—[(CH 2 ) j —NH] k —(CH 2 ) l —NH 2 , wherein i, j and l each independently of the others denotes from 2 to 4 and k denotes 0, 1, 2, 3 or 4; aminoamide, polyaminoamide, Mannich base, amine adduct; and aminoalkylsilane that includes at least one hydrolysable group; and the one or more aldehydes or ketones are of the formula (II), wherein: R 2 , R 3 each independently of the other denotes hydrogen or an unsubstituted or substituted organic radical which includes at least one aliphatic, heteroaliphatic, alicyclic, or heterocyclic molecular structure; and the one or more aldehydes and/or ketones are compounds which have at least one or more primary and/or secondary hydrogen atoms at the carbon atom in the α-position to the carbonyl group; and the free-radical starter further comprises at least one aldehyde and/or ketone and as primary amine and one or more aminosilanised fillers that carry primary amino groups. 5. The hardener system according to claim 1 , wherein (b2) the imine which includes one or more imine structural increments of the formula (I) includes one or more aldimines as a reaction product of isobutyraldehyde and 3-aminopropyl-trimethoxysilane; of isobutyraldehyde and m-xylylenediamine; of isobutyraldehyde and 1,3-bis(aminomethyl)-cyclohexane; of isobutyraldehyde and amine-functionalised polyoxyalkylene; isophoronediamine; of isobutyraldehyde and; of isobutyraldehyde and diethyltoluenediamine; and of isobutyraldehyde and cyclohexane-1,2-diamine; or mixtures of two or more of those reaction products. 6. The hardener system according to claim 1 , wherein: the activator in the form of a metal salt comprises one or more salts of organic and/or inorganic acid with one or more metals, the one or more metals comprising one or more of copper, iron, vanadium, manganese, cerium, cobalt, zirconium, and bismuth; the inorganic acid comprising one or more of a sulfate radical and a carbonate radical; and the organic acid comprising a carboxylate radical; and the free-radical starter comprises (b1) the at least one aldehyde and/or ketone and the at least one primary amine, the at least one aldehyde or ketone being of the formula (II), wherein: R 2 , R 3 each independently of the other denotes hydrogen or an unsubstituted or substituted organic radical which includes at least one aliphatic, heteroaliphatic, alicyclic or heterocyclic molecular structure; and the one or more aldehydes and/or ketones are compounds which have at least one or more primary and/or secondary hydrogen atoms at the carbon atom in the α-position to the carbonyl group; the at least one primary amine comprising one or more of mono-, di- and poly-amines, heteroalkyl- or heteroalkylene-(mono- or di-)amines, amine-functionalised polyoxyalkylenes, cycloalkyl- or cycloalkylene-(mono- or di)amines, heterocycloalkyl- or heterocycloalkylene-(mono- or di-)amines, arylalkyl- or arylalkylene-(mono- or di-)amines, aminosilanised fillers, aminoamides, polyaminoamides, Mannich bases or amine adducts and aminoalkylsilanes; wherein the constituents aldehyde and/or ketone on the one hand and the constituent primary amine on the other hand are divided separately between two components for mixing when the h

Assignees

Inventors

Classifications

  • of aromatic dialcohols · CPC title

  • in the form of urethane links · CPC title

  • C08F4/26Primary

    of manganese, iron group metals or platinum group metals · CPC title

  • in the substrate · CPC title

  • Presence of (meth)acrylic polymer · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10544235B2 cover?
A hardener system for a synthetic resin composition having free-radical-polymerisable compounds, which includes the following constituents: a) at least one activator in the form of a metal salt, and as free-radical starter b1) (i) at least one aldehyde and/or ketone and at least one primary amine, and/or b2) (ii) at least one aldimine or (iii) at least one ketimine, or a mixture of two or more …
Who is the assignee on this patent?
Fischerwerke Gmbh & Co Kg
What technology area does this patent fall under?
Primary CPC classification C08F4/26. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 28 2020 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 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).