Use of an Epoxide-Amine-Based Multicomponent Mortar Composition

US2016159690A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016159690-A1
Application numberUS-201414905664-A
CountryUS
Kind codeA1
Filing dateJul 18, 2014
Priority dateJul 18, 2013
Publication dateJun 9, 2016
Grant date

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Described is the use of a hardening composition for epoxide-amine-based, multicomponent mortar compositions, particularly the use of one of these epoxide-amine-based, multicomponent mortar compositions for chemical fastening purposes. The multicomponent mortar composition contains (A) a resin component, which comprises as a curable compound at least an epoxide resin and optionally at least one reactive diluent, and (B) a hardener component, which comprises a hybrid hardener, wherein the resin component (A) and/or the hardener component (B) optionally comprises other ingredients selected from among inorganic and/or organic compounds. The hybrid hardener is a mixture of (a) at least one amine, selected from among aliphatic, alicyclic, or aromatic amines, as a hardener, and (b) a novolac resin as catalyst, wherein the novolac resin is contained in a quantity of 30 to 45 percent by weight, relative to the total weight of the hybrid hardener. The use of the hybrid hardener results in a rapid curding of the multicomponent mortar composition, even at low temperatures, with a complete through-curing of the mortar composition. High load values of the cured mortar composition both at low temperatures (+5° C.) and at high temperatures (+50° C.) and improved creep resistance at high temperatures (+50° C.) are hereby achieved. In addition, one can entirely omit the use of free phenols.

First claim

Opening claim text (preview).

1 . Use of a hybrid hardener which contains a mixture of (a) at least one amine, selected from among aliphatic, alicyclic and aromatic amines, wherein the amine on average has at least two reactive hydrogen atoms, bonded to a nitrogen atom, per molecule, as a hardener and (b) a novolac resin of the general formula (I): in which R 1 , R 2 , R 3 and R 4 , each independent of each other, are hydrogen or an unbranched or branched C 1 -C 15 alkyl radical and n is 1 to 12, wherein the novolac resin is contained in a quantity of 30 to 45 percent by weight, relative to the total weight of the hybrid hardener (a) and (b), as a catalyst, as a hardener in an epoxide-based, multicomponent mortar composition. 2 . Use according to claim 1 , wherein in formula (I), R 1 to R 4 are hydrogen, or one or two of the radicals R 1 to R 4 are CH 3 radicals, or one of the radicals R 1 to R 4 is a tert-butyl radical or an unbranched or branched C 8 -C 15 alkyl radical. 3 . Use according to claim 1 , wherein the hardener contains a mixture of at least two amines, selected from among aliphatic, alicyclic and aromatic amines. 4 . Use according to claim 3 , wherein the mixture contains (i) alkyl diamine and aromatic amines or (ii) alkyl diamines, polyalkylene-polyamine and aromatic amines. 5 . Use according to claim 4 , wherein the mixture contains (i) 2-methyl-1,5 -pentanediamine and 1,3-benzenedimethanamine or (ii) trimethylhexamethylenediamine, 2-methyl-pentanediamine, triethylenetetramine and 1,3-benzenedimethanamine. 6 . Use according to claim 5 , wherein the mixture contains (i) 28 to 34 percent by weight 2-methyl-1,5-pentanediamine and 4 to 7 percent by weight 1,3-benzenedimethanamine, or (ii) 20 to 28 percent by weight trimethylhexamethylenediamine, 20 to 28 percent by weight 2-methyl-pentanediamine, 10 to 18 percent by weight triethylenetetramine and 4 to 10 percent by weight 1,3-benzenedimethanamine, each relative to the hybrid hardener (a) and (b). 7 . Use according to claim 1 , wherein the hybrid hardener further contains (c) at least one compound of the general formula (II): in which R 1 is hydrogen or an unbranched or branched C 1 -C 15 alkyl radical; R 2 is a (CH 2 ) n NR 5 R 6 radical or a NH(CH 2 ) n NR 5 R 6 radical, in which R 5 , R 6 are, each independent of each other, an unbranched or C 1 -C 15 alkyl radical and n is 0 or 1; R 3 and R 4 are, each independent of each other, hydrogen or a (CH) n NR 7 R 8 radical or a NH(CH) n NR 7 R 8 radical, in which R 7 and R 8 are, each independent of each other, hydrogen or an unbranched or branched C 1 -C 15 alkyl radical and n is 0 or 1, as a co-catalyst. 8 . Use according to claim 7 , wherein in formula (II), R 1 is hydrogen, R 2 , R 3 and R 4 are each a (CH 2 ) n NR 7 R 8 radical with n=0 or 1, and R 7 and R 8 are methyl or ethyl. 9 . Use according to claim 8 , wherein the compound of the formula (II) is tris-2,4,6-(dimethyl aminomethyl)phenol. 10 . Use of a multicomponent mortar composition produced using the hybrid hardener according to claim 1 with (A) a resin component, which comprises as a curable compound at least one epoxide resin, which on average contains more than one epoxide group per molecule and optionally at least one reactive diluent; and (B) a hardener component, which comprises a hybrid hardener, wherein the resin component (A) and/or the hardener component (B) optionally contains additional ingredients, selected from among inorganic and organic compounds, for construction purposes, except coatings. 11 . Use according to claim 10 , in which the hybrid hardener is contained in a quantity of 54 to 84 percent by weight, relative to the hardener component (B). 12 . Use according to claim 10 , wherein the hardener component (B) further contains an adhesive agent. 13 . Use according to one of claim 10 , wherein the curable compound is selected from among diglycidyl ether of bisphenol A, diglycidyl ether of bisphenol F or mixtures thereof. 14 . Use according to claim 10 , wherein the resin component (A) further contains at least one reactive diluent. 15 . Use according to claim 14 , wherein the at least one reactive diluent is selected from among glycidyl ethers of aliphatic, alicyclic or aromatic mono- or polyalcohols, glycidyl ethers with an epoxide functionality of at least 2, tri or higher glycidyl ethers or mixtures of two or more thereof. 16 . Use according to claim 14 , wherein the reactive diluent is contained in a quantity of up to 60 percent by weight. 17 . Use according to claim 10 , wherein the resin component (A) and/or the hardener component (B) further contains at least one inorganic additive. 18 . Use according to claim 17 , wherein the at least one inorganic additive is selected from among mineral or mineral-like fillers, reinforcing agents, rheology auxiliary agents, phlegmatising agents, thixotropic agents, stabilizers, dispersing agents, agents for controlling the rate of reaction, and wetting agents. 19 . Use according to claim 17 , wherein the at least one inorganic additive is contained in a quantity of up to 70 percent by weight. 20 . Use according to claim 10 , for the structural adhesion of concrete/concrete, steel/concrete, or steel/steel or one of the mentioned material to other mineral materials, for the structural reinforcement of building components, masonry, and other mineral materials, for reinforcement applications with fiber-reinforced polymers for buildings, for the chemical fastening on surfaces of concrete, steel, or other mineral materials.

Assignees

Inventors

Classifications

  • Amines, polyamines · CPC title

  • C04B26/14Primary

    Polyepoxides · CPC title

  • C04B24/302Primary

    Phenol-formaldehyde condensation polymers · CPC title

  • Phenols · CPC title

  • C08G59/56Primary

    together with other curing agents · CPC title

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What does patent US2016159690A1 cover?
Described is the use of a hardening composition for epoxide-amine-based, multicomponent mortar compositions, particularly the use of one of these epoxide-amine-based, multicomponent mortar compositions for chemical fastening purposes. The multicomponent mortar composition contains (A) a resin component, which comprises as a curable compound at least an epoxide resin and optionally at least one …
Who is the assignee on this patent?
Hilti Ag
What technology area does this patent fall under?
Primary CPC classification C04B26/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jun 09 2016 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).