Patent Application
20150252138
The invention relates to polyisocyanate polyaddition products and to the use of specific catalysts for their preparation, and to their use, in particular for the coating sector.
Polyurethane coatings have been known for a long time and are used in many fields. They are generally prepared from a polyisocyanate component and a hydroxyl component by mixing immediately before application (2K technology). For light-fast coatings there are generally used polyisocyanate components based on aliphatic polyisocyanates which, in comparison with products having aromatically bonded isocyanate groups, enter significantly more slowly into reaction with the hydroxyl component. In most cases, the reaction must therefore be catalysed, in particular when it is not possible or desirable to use very high reaction temperatures, even if heating is carried out where possible to further accelerate the reaction. Organic tin compounds, in particular dibutyltin dilaurate (DBTL), have proved to be successful as catalysts. Organotin compounds by definition have at least one Sn—C bond in the molecule. They have the general disadvantage of an unfavourable ecological profile, which has already led inter alia to the substance class of the organotin compounds being banned completely from marine paints, to which they were added as a biocide.
Organotin-free catalysts for the preparation of polyurethanes were and are therefore the focus of new developments. Such developments frequently turn to elements whose toxicological profile per se is judged to be less critical compared with organotin compounds, for example bismuth, titanium or zinc. A disadvantage of all those catalysts is, however, that they are not as universally usable as organotin compounds. Many of the catalysts discussed as alternatives exhibit disadvantages through to the complete loss of catalytic activity in a number of fields of application. Examples are the rapid hydrolysis of bismuth compounds in aqueous media, which renders them of no interest for the field of water-based coating technologies, which is becoming increasingly important now and in the future, and the sometimes unsatisfactory colour effects of titanium compounds in some lacquer formulations.
WO 2011/051247 describes the use of specific inorganic. Sn(IV) catalysts for accelerating the NCO—OH reaction, but with the additional property of accelerating that reaction only at elevated temperature and being as inactive as possible at room temperature (thermolatency).
Very generally, however, there are also fields of application in polyurethane chemistry in which the use of higher temperatures is not suitable, for example the construction sector. Instead, it is of interest here to effect rapid crosslinking, sometimes even at temperatures significantly lower than 20-25° C. (“room temperature”).
The object was, therefore, to bring the advantages of the thermolatent catalysts mentioned in WO 2011/051247 to bear while purposively circumventing the thermolatency, that is to say to maintain them at a comparable level compared with the prior-known, conventional organotin-based systems at the reaction temperature in question without having to increase the catalyst concentration (based on the same polyurethane matrix and “active” central atom) appreciably compared with the prior-known organotin catalysts of the prior art.
Surprisingly, it has been possible to achieve that object by adding protonic acids to the reaction mixture.
Accordingly, the invention provides polyisocyanate polyaddition products obtainable from
Preferably, D is —N(R1)—.
Preferably, R1 is hydrogen or an alkyl, aralkyl, alkaryl or aryl radical having up to 20 carbon atoms or the radical
particularly preferably hydrogen or an alkyl, aralkyl, alkaryl or aryl radical having up to 12 carbon atoms or the radical
most particularly preferably hydrogen or a methyl, ethyl, propyl, butyl, hexyl or octyl radical, wherein propyl, butyl, hexyl and octyl represent all isomeric propyl, butyl, hexyl and octyl radicals, Ph-, CH3Ph- or the radical
Preferably, D* is —O—.
Preferably, X, Y and Z are the alkylene radicals —C(R2)(R3)—, —C(R2)(R3)—C(R4)(R5)— or the ortho-arylene radical
Preferably, R2 to R7 are hydrogen or alkyl, aralkyl, alkaryl or aryl radicals having up to 20 carbon atoms, particularly preferably hydrogen or alkyl, aralkyl, alkaryl or aryl radicals having up to 8 carbon atoms, most particularly preferably hydrogen or alkyl radicals having up to 8 carbon atoms, yet more preferably hydrogen or methyl.
Preferably, R8 to R11 are hydrogen or alkyl radicals having up to 8 carbon atoms, particularly preferably hydrogen or methyl,
Preferably, L1, L2 and L5 are —NR12—, —S—, —SC(═S)—, —SC(═O)—, —OC(═S)—, —O—, or —OC(═O)—, particularly preferably —O— or —OC(═O)—.
Preferably, R12 is hydrogen or an alkyl, aralkyl, alkaryl or aryl radical having up to 20 carbon atoms, particularly preferably hydrogen or an alkyl, aralkyl, alkaryl or aryl radical having up to 12 carbon atoms, most particularly preferably hydrogen or a methyl, ethyl, propyl, butyl, hexyl or octyl radical, wherein propyl, butyl, hexyl and octyl represent all isomeric propyl, butyl, hexyl and octyl radicals.
Preferably, L3 and L4 are -Hal, —OH, —SH, —OR13, —OC(═O)R14, wherein the radicals R13 and R14 contain up to 20 carbon atoms, preferably up to 12 carbon atoms.
Particularly preferably, L3 and L4 are Cl—, MeO—, EtO—, BuO—, HexO—, OctO—, PhO—, formate, acetate, propanoate, butanoate, pentanoate, hexanoate, octanoate, laurate, lactate or benzoate, wherein Pr, Bu, Hex and Oct represent all isomeric propyl, butyl, hexyl and octyl radicals, yet more preferably Cl—, EtO—, BuO—, HexO—, OctO—, PhO—, hexanoate, laurate or benzoate, wherein Pr, Bu, Hex and Oct represent all isomeric propyl, butyl, hexyl and octyl radicals, Preferably, R15 to R20 are hydrogen or alkyl, aralkyl, alkaryl or aryl radicals having up to 20 carbon atoms, particularly preferably hydrogen or alkyl, aralkyl, alkaryl or aryl radicals having up to 12 carbon atoms, most particularly preferably hydrogen, methyl, ethyl, propyl, butyl, hexyl or octyl radicals, wherein propyl, butyl, hexyl and octyl represent all isomeric propyl, butyl, hexyl and octyl radicals.
The units L1-X, L2-Y and L5-Z preferably represent —CH2CH2O—, —CH2CH(Me)O—, —CH(Me)CH2O—, —CH2C(Me)2O—, —C(Me)2 CH2O— or —CH2C(═O)O—.
The unit L1-X-D-Y-L2 preferably represents: HN[CH2CH2O—]2, HN[CH2CH(Me)O—]2, HN[CH2CH(Me)O—][CH(Me)CH2O—], HN[CH2C(Me)2O—]2, HN[CH2C(Me)2O—][C(Me)2CH2O—], HN[CH2C(═O)O—]2, MeN[CH2CH2O—]2, MeN[CH2CH(Me)O—]2, MeN[CH2CH(Me)O—][CH(Me)CH2O—], MeN[CH2C(Me)2O—]2, MeN[CH2C(Me)2O—][C(Me)2CH2O—], MeN[CH2C(═O)O—]2, EtN[CH2CH2O—]2, EtN[CH2CH(Me)O—]2, EtN[CH2CH(Me)O—][CH(Me)CH2O—], EtN[CH2C(Me)2O—]2, EtN[CH2C(Me)2O—][C(Me)2CH2O—], EtN[CH2C(═O)O—]2, PrN[CH2CH2O—]2, PrN[CH2CH(Me)O—]2, PrN[CH2CH(Me)O—][CH(Me)CH2O—], PrN[CH2C(Me)2O—]2, PrN[CH2C(Me)2O—][C(Me)2CH2O—], PrN[CH2C(═O)O—]2, BuN[CH2CH2O—]2, BuN[CH2CH(Me)O—]2, BuN[CH2CH(Me)O—][CH(Me)CH2O—], BuN[CH2C(Me)2O—]2, BuN[CH2C(Me)2O—][C(Me)2CH2O—], BuN[CH2C(═O)O—]2, HexN[CH2CH2O—]2, HexN[CH2CH(Me)O—]2, HexN[CH2CH(Me)O—][(CH(Me)CH2O—], HexN[CH2C(Me)2O—]2, HexN[CH2C(Me)2O—][C(Me)2CH2O—], HexN[CH2C(═O)O—]2, OctN[CH2CH2O—]2, OctN[CH2CH(Me)O—]2, OctN[CH2CH(Me)O—][CH(Me)CH2O—], OctN[CH2C(Me)2O—]2, OctN[CH2C(Me)2O—][C(Me)2CH2O—], OctN[CH2C(═O)O—]2, wherein Pr, Bu, Hex and Oct can represent all isomeric propyl, butyl, hexyl and octyl radicals, PhN[CH2CH2O—]2, PhN[CH2CH(Me)O—]2, PhN[CH2CH(Me)O—][CH(Me)CH2O—], PhN[CH2C(Me)2O—]2, PhN[CH2C(Me)2O—][C(Me)2CH2O—], PhN[CH2C(═O)O—]2,
The tin compounds—as is known to the person skilled in the art—have a tendency to oligomerisation, so that polynuclear tin compounds or mixtures of mono- and poly-nuclear tin compounds are frequently present. In the polynuclear tin compounds, the tin atoms are preferably bonded with one another via oxygen atoms (“oxygen bridges”, vide infra). Typical oligomeric complexes (polynuclear tin compounds) form, for example, by condensation of the tin atoms via oxygen or sulfur, for example
where n>1 (see formula II). There are frequently found at low degrees of oligomerisation cyclic and at higher degrees of oligomerisation linear oligomers having OH or SH end groups (see formula III).
The invention further provides a process or the preparation of the polyisocyanate polyaddition products according to the invention, wherein
wherein the definitions given above apply for D, D*, Y, X and L1 to L4.
In cases where the tin compounds contain ligands having free OH and/or NH radicals, the catalyst can be incorporated into the product in the polyisocyanate polyaddition reaction. The particular advantage of such incorporable catalysts is their greatly reduced fogging behaviour, which is important especially when polyurethane coatings are used in automotive interiors.
The various preparation methods for the tin (IV) compounds to be used according to the invention or their tin (II) precursors are described inter alfa in: WO 2011/113926, J Organomet. Chem. 2009 694 3184-3189, Chem. Heterocycl. Comp. 2007 43 813-834, Indian J. Chem 1967 5 643-645 and in literature cited therein.
A number of cyclic tin compounds have already also been proposed for use as a catalyst for the isocyanate polyaddition process, see DD-A 242 617, U.S. Pat. No. 3,164,557, DE-A 1 111 377, U.S. Pat. No. 4,430,456, GB-A 899 948, US-A 2008/0277137. However, it is a common feature of all those prior-described systems of the prior art that the compounds in question are without exception Sn(II) or organotin (IV) compounds.
The catalysts can be combined with further catalysts/activators known from the prior art; for example, titanium, zirconium, bismuth, tin (II) and/or iron-comprising catalysts, such as are described, for example, in WO 2005/058996. The addition of amines or anticlines is also possible.
The catalyst according to the invention, optionally predissolved in a suitable solvent, can be added to the reaction mixture together with the NCO-reactive compound (polyol) or the polyisocyanate.
The same is true of the protonic acid to be used according to the invention. It can be used together with the catalyst, for example predissolved in one of the above-mentioned components, but optionally also separately, predissolved in the component that does not comprise the catalyst. A further advantage of the latter procedure is that catalysts which in themselves, that is to say in the absence of protonic acids, are comparatively inactive (which is disadvantageous) but which are generally also less active as regards the undesired reaction of the isocyanate groups with one another (which is advantageous) can be used in solution in the isocyanate component and it is nevertheless possible to obtain comparatively storage-stable preparations which develop the advantages according to the invention only after mixing with the reactant, generally an OH-functional polyether-, polyester-, polyacrylate- and/or polycarbonate-based polyol, which comprises the protonic acid, in the curing reaction.
The polyisocyanates (a) suitable for the preparation of polyisocyanate polyaddition products, in particular polyurethanes, are the organic aliphatic, cycloaliphatic, araliphatic and/or aromatic polyisocyanates having at least two isocyanate groups per molecule which are known per se to the person skilled in the art, and mixtures thereof. Examples of such polyisocyanates are di- or tri-isocyanates, such as, for example, butane diisocyanate, pentane diisocyanate, hexane diisocyanate (hexamethylene diisocyanate, HDI), 4-isocyanatomethyl-1,8-octane diisocyanate (triisocyanatononane, TIN), 4,4′-methylenebis(cyclohexyl isocyanate) 3,5,5-trimethyl-1-isocyanato-3-isocyanatomethylcyclohexane (isophorone di isocyanate, 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane (H6XDI), 1,5-naphthalene diisocyanate, diisocyanatodiphenylmethane (2,2′-, and 4,4′-MDI or mixtures thereof), diisocyanatomethylbenzene (2,4- and 2,6-toluene diisocyanate, TDI) and commercial mixtures of the two isomers, as well as 1,3-bis-(isocyanatomethyl)benzene (XDI), 3,3′-dimethyl-4,4′-biphenyl diisocyanate (TODD, 1,4-para-phenylene diisocyanate (PPDI) as well as cyclohexyl diisocyanate (CHDI) and the higher molecular weight oligomers with biuret, uretdione, isocyanurate, iminooxadiazinedione, allophanate, urethane and carbodiimideluretonimine structural units obtainable individually or in a mixture from the above. Preference is given to the use of polyisocyanates based on aliphatic and cycloaliphatic diisocyanates.
The polyisocyanate component (a) can be present in a suitable solvent. Suitable solvents are those which exhibit sufficient solubility of the polyisocyanate component and are free of isocyanate-reactive groups. Examples of such solvents are acetone, methyl ethyl ketone, cyclohexanone, methyl isobutyl ketone, methyl isoamyl ketone, diisobutyl ketone, ethyl acetate, n-butyl acetate, ethylene glycol diacetate, butyrolactone, diethyl carbonate, propylene carbonate, ethylene carbonate, N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, methylal, ethylal, butylal, 1,3-dioxolane, glycerol formal, benzene, toluene, n-hexane, cyclohexane, solvent naphtha, 2-methoxypropyl acetate (MPA).
The isocyanate component can additionally comprise conventional auxiliary substances and added ingredients, such as, for example, rheology improvers (for example ethylene carbonate, propylene carbonate, dibasic esters, citric acid esters), UV stabilisers (for example 2,6-dibutyl-4-methylphenol), hydrolytic stabilisers (for example sterically hindered carbodiimides), emulsifiers and catalysts (for example trialkylamines, diazabicyclooctane, tin dioctoate, dibutyltin dilaurate. N-alkylmorpholine, lead, zinc, tin, calcium, magnesium octoate, the corresponding naphthenates and p-nitrophenolate and/or also inercuryphenyl neodecanoate) and fillers (for example chalk), colourants which can optionally be incorporated into the polyurethane/polyurea to be formed later (which accordingly have Zerewitinoff-active hydrogen atoms) and/or colouring pigments.
As NCO-reactive compounds (b) there can be used all compounds known to the person skilled in the art which have a mean OH or NH functionality of at least 1.5. They can be, for example, low molecular weight diols (e.g. 1,2-ethanediol, 1,3- and 1,2-propanediol, 1,4-butanediol), triols (e.g. glycerol, trimethylolpropane) and tetraols (e.g. pentaerythritol), short-chained polyamines but also higher molecular weight polyhydroxy compounds such as polyether polyols, polyester polyols, polycarbonate polyols, polysiloxane polyols, polyamines and polyether polyamines as well as polybutadiene polyols. Polyether polyols are obtainable in a manner known per se by alkoxylation of suitable starter molecules with base catalysis or using double metal cyanide compounds (DMC compounds). Suitable starter molecules for the preparation of polyether polyols are, for example, simple, low molecular weight polyols, water, organic polyamines having at least two N—H bonds or arbitrary mixtures of such starter molecules. Preferred starter molecules for the preparation of polyether polyols by alkoxylation, in particular by the DMC process, are in particular simple polyols such as ethylene glycol, 1,3-propylene glycol and 1,4-butanediol, 1,6-hexanediol, neopentyl glycol, 2-ethyl-1,3-hexanediol, glycerol, trimethylolpropane, pentaerythritol as well as low molecular weight, hydroxyl-group-comprising esters of such polyols with dicarboxylic acids of the type mentioned by way of example below, or low molecular weight ethoxylation or propoxylation products of such simple polyols, or arbitrary mixtures of such modified or unmodified alcohols. Alkylene oxides suitable for the alkoxylation are in particular ethylene oxide and/or propylene oxide, which can be used in the alkoxylation in any desired sequence or also in admixture. Polyester polyols can be prepared in known manner by polycondensation of low molecular weight polycarboxylic acid derivatives, such as, for example, succinic acid, adipic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, tetrachlorophthalic anhydride, endomethylenetetrahydrophthalic anhydride, glutaric anhydride, maleic acid, maleic anhydride, fumaric acid, dimer fatty acid, trimer fatty acid, phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, citric acid or trimellitic acid, with low molecular weight polyols, such as, for example, ethylene glycol, diethylene glycol, neopentyl glycol, hexanediol, butanediol, propylene glycol, glycerol, trimethylolpropane, 1,4-hydroxymethylcyclohexane, 2-methyl-1,3-propanediol, 1,2,4-butanetriol, triethylene glycol, tetraethylene glycol, polyethylene glycol, dipropylene glycol, polypropylene glycol, dibutylene glycol and polybutylene glycol, or by ring-opening polymerisation of cyclic carboxylic acid esters, such as ε-caprolactone. In addition, hydroxycarboxylic acid derivatives, such as, for example, lactic acid, cinnamic acid or ω-hydroxycaproic acid, can be polycondensed to polyester polyols. However, polyester polyols of oleochemical origin can also be used. Such polyester polyols can be prepared, for example, by complete ring opening of epoxidised triglycerides of an at least partially olefinically unsaturated fatty-acid-comprising mixture with one or more alcohols having from 1 to 12 carbon atoms and by subsequent partial transesterification of the triglyceride derivatives to alkylester polyols having from 1 to 12 carbon atoms in the alkyl moiety. The preparation of suitable polyacrylate polyols is known per se to the person skilled in the art. They are obtained by radical polymerisation of hydroxyl-group-comprising, olefinically unsaturated monomers or by radical copolymerisation of hydroxyl-group-comprising, olefinically unsaturated monomers with optionally other olefinically unsaturated monomers, such as, for example, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, isobornyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, isobornyl methacrylate, styrene, acrylonitrile and/or methacrylonitrile. Suitable hydroxyl-group-comprising, olefinically unsaturated monomers are in particular 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, the hydroxypropyl acrylate isomer mixture obtainable by addition of propylene oxide to acrylic acid, and the hydroxypropyl methacrylate isomer mixture obtainable by addition of propylene oxide to methacrylic acid. Suitable radical initiators are those from the group of the azo compounds, such as, for example, azoisobutyronitrile (AIBN), or from the group of the peroxides, such as, for example, di-tert-butyl peroxide.
Preferably, b) is higher molecular weight polyhydroxy compounds.
Component (b) can be present in a suitable solvent. Suitable solvents are those which exhibit sufficient solubility of the component. Examples of such solvents are acetone, methyl ethyl ketone, cyclohexanone, methyl isobutyl ketone, methyl isoamyl ketone, diisobutyl ketone, ethyl acetate, n-butyl acetate, ethylene glycol diacetate, butyrolactone, diethyl carbonate, propylene carbonate, ethylene carbonate, N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, methylal, ethylal, butylal, 1,3-dioxolane, glycerol formal, benzene, toluene, n-hexane, cyclohexane, solvent naphtha, 2-methoxypropyl acetate (MPA). In addition, the solvents can also carry isocyanate-reactive groups, Examples of such reactive solvents are those which have a mean functionality of isocyanate-reactive groups of at least 1.8, They can be, for example, low molecular weight diols (e.g. 1,2-ethanediol, 1,3- and 1,2-propanediol, 1,4-butanediol), triols (e.g. glycerol, trimethylolpropane), but also low molecular weight diamines, such as, for example, polyaspartic acid esters.
The process for the preparation of the polyisocyanate polyaddition products can be carried out in the presence of conventional rheology improvers, stabilisers, UV stabilisers, catalysts, hydrolytic stabilisers, emulsifiers, fillers, optionally incorporable colourings (which accordingly have Zerewitinoff-active hydrogen atoms) and/or colouring pigments. The addition of zeolites is also possible.
Preferred auxiliary substances and added ingredients are blowing agents, fillers, chalk, carbon black or zeolites, flame retardants, colouring pastes, water, antimicrobial agents, flow improvers, thixotropic agents, surface-modifying agents and retarders in the preparation of the polyisocyanate polyaddition products. Further auxiliary substances and added ingredients include antifoams, emulsifiers, foam stabilisers and cell regulators. An overview is given in G. Oertel, Polyurethane Handbook, 2nd Edition, Carl Hanser Verlag, Munich, 1994, Chap. 3.4.
The protonic acids to be used according to the invention can be selected as desired from a large number of substances which appear to the person skilled in the art to be suitable for this purpose. It is important only that they do not enter into negative interactions with the polyurethane matrix or lead to incompatibilities, which can be achieved almost arbitrarily by a suitable choice of the molecular structure of the radical X— in the protonic acid HX. It is also possible for the protonic acid to be bonded via the radical X in the polymer matrix of the reactant b), which generally carries OH groups, for the isocyanate component a). Thus, many polyacrylates of the prior art comprise acidic protons from the incorporation of (meth)acrylic acid units during their preparation. The resulting acid number is sometimes even so high that the thermolatency of the catalyst system according to the invention suffers, which can readily be adjusted to the desired extent by means of simple preliminary tests with purposive variation of the acid number, buffering with suitable bases, etc.
Finally, it is also possible for the protonic acid to be used according to the invention not to be generated until the curing reaction from suitable precursors such as acid anhydrides, halides, etc., for example by the action of (atmospheric) moisture.
The systems according to the invention can be applied to the object to be coated in solution or from the melt as well as, in the case of powder coatings, in solid form by methods such as brushing, rolling, pouring, spraying, dipping, fluidised bed processes or by electrostatic spraying processes. Suitable substrates are, for example, materials such as metals, wood, plastics materials or ceramics.
Accordingly, the invention further provides coating compositions comprising the polyisocyanate polyaddition products according to the invention, and coatings obtainable therefrom, and substrates coated with those coatings.
The invention is to be explained in greater detail by means of the following examples. In the examples, all percentages are to be understood as being percentages by weight, unless indicated otherwise. All reactions were carried out under a dry nitrogen atmosphere. The catalysts from Table 1 were obtained by standard literature procedures (see Chem. Heterocycl. Comp. 2007 43 813-834 and literature cited therein), DBTL was obtained from Kever Technologic, Ratingen, D.
For better comparability of the activity of the tests carried out by the procedure according to the invention with the comparative examples, the amount of catalyst was given as mg of Sn per kg of (solvent-free) polyisocyanate curing agent (ppm), wherein the commercial product Desmodur®N 3300 from Bayer MaterialScience AG, Leverkusen, DE was used as the polyisocyanate curing agent, and exactly one equivalent (based on the free isocyanate groups of the polyisocyanate curing agent) of triethylene glycol monomethyl ether, TEGMME (product of Aldrich, Taufkirchen, D) was used as the model compound for the isocyanate-reactive component (‘poly’ol). By adding 10% (based on Desmodur® N 3300) n-butyl acetate, it was ensured that samples having a sufficiently low viscosity could be taken throughout the course of the reaction, which permit precise determination of the NCO content by means of titration according to DIN 53 185. The NCO content calculated at the start of the reaction without any NCO—OH reaction is 10.9+/−0.1%, tests in which the NCO content had fallen to 0.1% or in which the NCO content was still more than 6% after 4 hours reaction time were terminated.
Comparative test 1 at a constant 30° C. shows the extremely slow fall in the NCO content of the mixture in the uncatalysed case (Table 2, test 1). Comparative test 2 represents the “standard case” carried out according to the prior art with dibutyltin dilaurate. Comparative tests 3 to 6 demonstrate the low or non-existent activity, known from WO 2011/051247, of the inorganic stannacycles, here cat. 1-4, for the acceleration of the NCO—OH reaction at 30° C. (“room temperature”). Examples 7-15 according to the invention show that it is only by adding the indicated amount of acid that the thermolatency can purposively be broken and a rapid NCO—OH reaction can be effected even at 30° C. As is apparent from a comparison of Examples 7 and 8 according to the invention, on the one hand, and 9-15, on the other hand, the same amount of acid can have effects in respect of the acceleration of the reaction at 30° C. which differ greatly in extent with different catalysts. The optimum desired for a particular use is therefore always to be determined by preliminary tests.
1) Sn [ppm] on polyisocyanate curing agent, solvent-free;
2)[%] acetic acid on TEGMME,
3)after 97 h at 30° C.: 8.9% NCO
Solutions, saturated by stirring for 3 days at 50° C. with excess catalyst 1 or 2 (solid) and then filtered, of
After being stored for 6 months, the mixture from Example 16a) had gelled completely. The mixture from Example 16b), on the other hand, had changed only slightly and had the following data: 21.9% NCO content, 1860 mPas at 23° C.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12185930.0 | Sep 2012 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/069615 | 9/20/2013 | WO | 00 |
