Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From phenol – phenol ether – or inorganic phenolate
Reexamination Certificate
1999-10-06
2002-03-05
Lovering, Richard D. (Department: 1712)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From phenol, phenol ether, or inorganic phenolate
C521S135000, C521S178000, C525S484000, C528S109000
Reexamination Certificate
active
06353081
ABSTRACT:
STATE OF THE ART
Curing of epoxy resins with metal complexes is known from the literature: Examples are U.S. Pat. Nos. 3,553,166, 3,638,007, 3,792,016, 4,101,514 and DE-A 2300489 which disclose differing metal complexes which are used as curing agents for epoxy resins. They all have the disadvantage that they only develop their curing function at a speed sufficient for technical requirements above 160-220° C. At these high temperatures, cleavage products are formed which lead to poor network structures and thus cause negative polymer properties such as shrinkage, water absorption or the like.
Through the combined use of these curing agents with auxiliary bases, the cure temperatures can be slightly decreased and the acceleration effect can be controlled. Such systems, on the one hand, are cost-intensive and have the further disadvantage that the auxiliary bases react with epoxide groups leading to degradation of the polymer properties.
WO 91/13925 discloses metal complexes which can be used as latent curing agents for epoxy resins which have a significantly lower cure temperature. However, epoxy resin systems comprising these curing agents are stable in storage only up to 80° C. However, with processing techniques, such as, for example, the RIM (Reaction Injection Molding) or RTM (Resin Transfer Molding) technique, epoxy resin curing agent systems are required which are stable for several hours at temperatures up to 100° C., but which, at temperatures in the range of 120 to 160° C., cure very rapidly and as completely as possible.
OBJECTS OF THE INVENTION
It is an object of the invention to provide curing agents for epoxy compounds which can be used as the sole curing agents, which thus yield homogeneous polymer mixtures whose mixtures with epoxy resins are stable in storage for several hours up to temperatures of 100° C. and which, in the temperature range of 120 to 160° C., preferably in the temperature range of 120 to 140° C., cure rapidly and as completely as possible and which thus make possible the production of formed parts in fixed-cycle operation and of good quality by means of RIM, RTM and comparable processing techniques.
These and other objects and advantages of the invention will become obvious from the following detailed description.
THE INVENTION
The curing agents of the invention are comprised of a compound selected from the group consisting of
M(X)
n
and M(X)
n
(L)
o
wherein M is a bivalent or trivalent cation of a complexing metal, X is a pseudohalogen anion, L is a nitrogen-containing ligand, n is 2 or 3 and o is 1 or 2.
The curing agents of the invention are useful in curing mixtures containing epoxy resin molding materials for use in RIM and RTM techniques and comparable molding and shaping processes. They are also useful as curing agents for adhesive compositions containing epoxy resins and prepregs. When used with acid anhydrides, the curing agents may be used in the production of epoxy resin foams.
CH-A 484 867, CH-A 496 749 and EP-A 0 682 053 teach the use of pseudohalogen metal compounds or complexes of pseudohalogenide metal compounds with nitrogen bases in systems comprising epoxy resins. However, the compounds in these systems do not function as curing agents, but only as accelerators for the curing agents proper. Through side reactions of the accelerators during the curing, non-homogeneous polymer mixtures are formed in such systems.
It has been found that mixtures of epoxy resins and compounds of the formula:
M(X)
n
or M(X)
n
(L)
o
wherein M is a bi- or trivalent cation of a complexing metal, X is a pseudohalogen anion, L is a nitrogen-containing ligand, n is 2 or 3, and o is 1 or 2 are processible up to several hours in the temperature range up to 100° C. and cure rapidly and as completely as possible in the temperature range from 120 to 160° C., so that postcuring of shaped parts produced and cured accordingly becomes substantially superfluous. Consequently, these compounds can be used as sole epoxy resin curing agents which, additionally, surprisingly correspond in their curing properties to the property profile required for some applications.
It has, furthermore, been found that epoxy resins cured with compounds of the formula
M(X)
n
or M(X)
n
(L)
o
wherein M, X, L, n and o have the above indicated definitions, exhibit improved behavior in fire. To exhibit defined responses indicating flame retardance, corresponding mixtures require approximately 30% less of additional flame-resistant agents than is necessary with epoxy resin mixtures cured by the prior art.
It was, moreover, found that mixtures comprising epoxy resins and compounds of the formulae
M(X)
n
or M(X)
n
(L)
o
wherein M, X, L, n and o have the above indicated definitions, form highly homogeneous foams if they are subjected, together with acid anhydrides as additional curing agents, to the anhydride curing process known per se.
The curing agents of the invention are compounds of complexing, bi- or trivalent metal ions with pseudohalogenides as well as complexes of such compounds with nitrogen-containing ligands in very low coordination number. Metal ions for these compounds are ions of bi- or trivalent principal group metals such as Mg, Ca or Al ions, as well as bi- or trivalent ions of transition group metals, particularly Mn, Fe, Co, Ni, Cu or Zn ions.
Pseudohalogenides are ions which comprise at least two electronegative elements. Examples thereof are cyanate, cyanide, thiocyanate, selenocyanate, azide or cyanamide ions. Preferred pseudohalogenides are cyanates and thiocyanates.
The nitrogen-containing ligands are mono- or polydentate nitrogen donors which can occupy at least one coordination site on the metal atom. Examples of these ligands are imidazoles, primary, secondary and tertiary aliphatic, cycloaliphatic or aromatic amines, pyrazoles, quinolines or pyridines. Preferred nitrogen-containing ligands are N-alkylimidazoles, tertiary amines and pyridines.
The production of the compounds of formula M(X)
n
takes place in a manner known per se by stoichiometric conversion of the alkali or ammonium salts of the pseudohalogenides with salts of the corresponding complexing metals in aqueous solution. The anions of these salts can be selected in any desired way as long as the salts are water-soluble. Preferred are cost-effective salts such as halides, sulfates, nitrates, perchlorates or acetates.
For the production of the complexes of formula M(X)
n
(L)
o
, the prior art taught to dissolve metal salts, salts of the pseudohalogenides and nitrogen-containing ligands in a polar organic solvent, preferably ethanol, and to mix these solutions in stoichiometric proportions of the reactants. To accelerate the crystallization of the complexes, a further, less polar solvent was added to the reaction mixture (J. Inorg. Nucl. Chem. 39 (1977), 216-217).
In contrast, it was found that the complexes M(X)
n
(L)
o
can be produced in a simple manner wherein the water-soluble metal salts, alkali or ammonium salts of the pseudohalogenides and ligands in aqueous solutions are mixed in approximately stoichiometric proportions of the reactants. Only in the case of ligands which are sparingly soluble in water is it recommended to add to these solutions additionally an organic solvent functioning as a solubilizing agent. Solvents such as ethanol, propanol, dimethylformamide or dimethylsulfoxide can be used in quantities of 0.1 to 25 percent by weight relative to the total reaction mixture. After a short reaction time, the complexes produced according to the invention precipitate in high yields either as solid substances in the form of fine-particle crystals or they separate out at high temperatures as liquid products and can be separated, purified and dried in a manner known per se. As a function of the selected isolation method (separation as liquid phase or as finely dispersed powder), the conversion temperature is selected in the range from 20 to 100° C.
Surprisingly, the complexes are precipitated in pure form without the use of an auxiliary base, i.e. neither in the form of mixed complexes with
Dey Holger
Doring Manfred
Palinsky Andreas
Wuckelt Jorg
Bakelite AG
Bierman, Muserlian and Lucas
Lovering Richard D.
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