Aminotriazine derivatives containing glycol ether and their use in coating resins

BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to binders comprising
A) an aminotriazine derivative in which the primary amino groups of the triazine are methylolated on average with at least one mole of formaldehyde per mole of primary amino groups, and these methylol groups are etherified on average with at least 0.5 mol of primary alcohol per mole of methylol group and the primary alcohols are a mixture containing
a) 0.5-99.5 mol % of a C.sub.1 -C.sub.4 -alkanol and
b) 99.5-0.5 mol % of an alcohol of the formula
R.sup.1 --O--�R.sup.2 --O!.sub.n --R.sup.3 --OH I,
in which R.sup.1 is C.sub.1 -C.sub.24 -alkyl or C.sub.6 -C.sub.12 -aryl which may be unsubstituted or substituted by from one to three C.sub.1 -C.sub.8 -alkyl groups, and R.sup.2 and R.sup.3 independently of one another are C.sub.2 -C.sub.8 -alkylene and n is an integer from 1 to 100, or of a mixture of higher-boiling alcohols having a boiling point of above 120.degree. C. at 1 bar which contains at least 10 mol %, based on the higher-boiling alcohols, of alcohols of the formula I, and
B) a radical polymer, polycondensation product or polyadduct which is crosslinkable with the aminotriazine derivative.
The invention also relates to an aminotriazine derivative in which the primary amino groups of the triazine are methylolated on average with at least one mole of formaldehyde per mole of primary amino groups, and these methylol groups are etherified on average with at least 0.5 mol of primary alcohol per mole of methylol group, and the primary alcohol is a mixture containing
a) 50-99.5 mol % of a C.sub.1 -C.sub.4 -alkanol and
b) 0.5-50 mol % of an alcohol of the above formula I or of a mixture of higher-boiling alcohols having a boiling point above 120.degree. C. at 1 bar which contains at least 10 mol %, based on the higher-boiling alcohols, of alcohols of the formula I.
2. Discussion of the Background
Highly methylolated aminotriazines which are etherified to a large extent with short-chain alcohols melamine being a particular example of such aminotriazines, are used as crosslinking agents for hydroxyl-containing polymers in coating binders.
In comparison with aminotriazine derivatives having high proportions of free NH and OH groups a high degree of alkylation and etherification results in a lower solution viscosity, enabling the production of medium-solids and, in particular, high-solids coating materials. Coating compositions of this kind with a reduced content of volatile solvents are preferred on ecological grounds (lower emission of organic carbon) and offer the paint user cost advantages (lower expenditure on solvent reprocessing or incinerations. At the same time, however, a high degree of alkylation and etherification leads to a level of reactivity, in the crosslinking of OH-containing coating binders, which is reduced in relation to partially methylolated and partially etherified aminotriazine derivatives.
This lower reactivity can be compensated only by using higher baking temperatures, with the disadvantage of the higher consumption of energy and the yellowing of the coated surfaces, or by the increased addition of acidic catalysts, acids and/or their amine salts, with the disadvantage of a reduced weather resistance (hydrophilic acid remains in the coating).
DE-A 24 14 426 discloses methylolaminotriazines etherified with ethylene glycol monoethyl ether and their use as crosslinking agents for hydroxyl-containing polymers. However, the reactivity of these aminotriazine derivatives for crosslinking with hydroxyl groups remains inadequate.
DE-A-36 32 587 describes melamine-formaldehyde resins which are etherified with glycol ethers, one example being polyethylene glycol, or with other alcohols as well as the glycol ethers. Basically, however, glycol ethers are present in mixtures in a distinct excess. The resins are prepared by the simultaneous reaction of melamine, formaldehyde and glycol ethers in a substantially anhydrous process which entails the use of paraformaldehyde.
SUMMARY OF THE INVENTION
It is an object of the present invention to prepare aminotriazine derivatives whose low solution viscosity renders them suitable for the production of low-solvent coating materials and which have a markedly increased reactivity with OH-containing binders in comparison with the conventional resins such as, for example, hexamethoxymethylmelamine resins.
Other desirable properties are good elasticity, good compatibility of the aminotriazine derivatives with the other components of binders, for example for coating materials, and good performance properties of binders containing the aminotriazine derivatives.
We have found that this object is achieved by the binders defined at the outset, in which the aminotriazine derivatives A) are at least partially methylolated and etherified aminotriazines.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Examples of suitable aminotriazines are melamine, benzoguanamine, acetoguanamine and bisguanamine such as adipo-, glutaro- or methylglutarobisguanamine, and spiroguanamines. Other suitable compounds are those which contain two or more aminotriazine moieties which may, for example, be condensed.
Preference is given to melamine and to compounds which contain two or more melamine moieties, for example from 2 to 5 melamines bridged via methylol groups, or mixtures thereof. Such mixtures of melamines and melamine resins with higher levels of condensation preferably contain at least 40 mol % of melamine. Melamine itself is particularly preferred.
The aminotriazines are methylolated with on average at least 1 mol, preferably at least 1.4 mol and particularly preferably with at least 1.7 mol of formaldehyde per mole of primary amino groups, and these methylol groups are etherified on average with at least 0.5 mol, preferably at least 0.6 mol and particularly preferably at least 0.7 mol of a mixture of primary alcohols per mole of methylol group.
This mixture contains
a) from 0.5 to 99.5 mol %, preferably from 50 to 99.5 mol %, particularly preferably from 85 to 99.5 mol % and very especially from 90 to 99 mol %, based on the mixture, of a C.sub.1 -C.sub.4 -alkanol and
b) from 99.5 to 0.5 mol %, preferably from 50 to 0.5 mol %, particularly preferably from 15 to 0.5 mol % and very especially from 10 to 1 mol %, based on the mixture, of an alcohol of the above formula I or of a mixture of higher-boiling alcohols having a boiling point of above 120.degree. C. at 1 bar which contains at least 10 mol %, preferably at least 30 mol % and particularly preferably at least 60 mol % of an alcohol of the formula I.
Suitable C.sub.1 -C.sub.4 -alkanols are all those having a boiling point of below 120.degree. C. at 1 bar, preference being given to methanol, isobutanol or n-butanol and mixtures of such alkanols.
Preferred alcohols of the formula I are those in which R.sup.1 is C.sub.1 -C.sub.24 alkyl, preferably C.sub.1 -C.sub.6 -alkyl, R.sup.2 and R.sup.3 independently of one another are C.sub.2 -C.sub.8 -alkylene, preferably C.sub.2 -C.sub.4 -alkylene and particularly preferably are both ethylene, and n is an integer from 1 to 20, preferably from 1 to 5.
Examples of alkanols of the formula I are di-, tri- or tetraethylene glycol monomethyl ether and the corresponding monobutyl ethers.
Higher-boiling alcohols having a boiling point >120.degree. C. at 1 bar, which can be employed as a mixture with the alcohols of the formula I, are preferably those having up to 20 carbon atoms and no further hetero atoms. Examples are n-pentanol, 2-pentanol, cyclopentanol, 2-methylbutanol, 3-methyl-1-butanol, cyclohexanol, 4-methyl-2-pentanol, methylcyclohexanol, hexahydrobenzyl alcohol, 2,4-di-methyl-3-pentanol, 2-ethylhexanol, nonanol, decanol, oxo alcohols and fatty alcohols where the chain is from 12 to 20 carbon atoms long, such as lauryl alcohol, tridecanol, myristyl alcohol, cetyl alcohol, stearyl alcohol or oleyl alcohol, and aryl-containing alcohols such as benzyl alcohol, o-, m- or p-methylbenzyl alcohol, 1-phenylethanol, 2-phenylethanol, .alpha.-ethylbenzyl alcohol, .alpha.-isopropylbenzyl alcohol, hydroxymethylnaphthalene and 1-(.alpha.-hydroxyethyl)naphthalene.
The aminotriazine derivatives A) are preferably prepared by transacetalization of aminotriazines which are methylolated in accordance with the abovementioned degree of methylolation and/or are etherified in accordance with the abovementioned degree of etherification and exclusively with the C.sub.1 -C.sub.4 -alkanols a). For transetherification the alcohols b) are added to these aminotriazine derivatives. The alcohols b) may be employed in only a slight excess based on the desired content of these alcohols in the aminotriazine derivative.
The transacetalization is generally carried out without the addition of solvents. The addition of solvents is possible in principle, in which case they are preferably either the alcohol a) present in the starting product and therefore, for example, methanol, ethanol, n-butanol or isobutanol, or are aprotic solvents which are unable to react with the substances employed under the reaction conditions. Examples of such solvents include ethers such as diethyl ether, diisopropyl ether, methyl tertbutyl ether, tetrahydrofuran, dioxane and 1,2-dimethoxyethane, aromatic solvents such as benzene, toluene, xylene and isopropylbenzene, or halogenated hydrocarbons such as di-, tri- and tetrachloromethane, di-, tri- and tetrachloroethane and chlorobenzene.
The reaction is preferably carried out with acid catalysis using organic and/or inorganic acids which in water at 25.degree. C. have a pK <4, examples being citric acid, tartaric acid, lactic acid, chloroacetic acid, trichloroacetic acid, formic acid, oxalic acid, malonic acid, maleic acid, fumaric acid, phthalic acid, o-nitrobenzoic acid, o-chlorobenzoic acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, naphthalenesulfonic acid, hydrochloric acid, nitric acid, sulfuric acid and phosphoric acid. Also suitable are Lewis acids such as, for example, boron trifluoride or aluminum chloride.
The reaction is generally carried out at from 40.degree. to 150.degree. C., preferably at from 60.degree. to 120.degree. C., and at atmospheric or reduced pressure. Carrying out the reaction at a reduced pressure of, for example, from 1.5 to 500 mbar, preferably from 10 to 200 mbar, enables volatile constituents of the reaction mixture, predominantly the alcohol a) present in the starting product, to be removed by distillation during the reaction, thereby enabling the reaction equilibrium to be shifted in the direction of the products and high conversions of the alcohols b) to be achieved.
When the desired degree of conversion has been reached, which is at least 60% and preferably 80% based on the alcohols b) employed and is measured by the decrease in the alcohols b) or by the increase in the liberated alcohol a), the reaction is ended. This is achieved just by lowering the temperature or by also neutralizing the acid catalyst with bases such as, for example, aqueous or alcoholic sodium hydroxide or potassium hydroxide solution, or with alkylamines such as triethylamine, tri-n-propylamine, tributylamine, tri-2-ethylhexylamine, dimethylethylamine or alkanolamines such as diethanolamine, triethanolamine, triisopropanolamine, dimethylethanolamine, diethylethanolamine, dibutylethanolamine, methyldiethanolamine or butyldiethanolamine.
The transacetalization may be carried out in one or more steps. In the case of alcohol mixtures b) the reaction can, for example, be carried out first with an alcohol, up to a degree of conversion of at least 60%, after which further acid catalyst and the remaining alcohol(s) may be added and the reaction continued.
The reaction may be followed by a further distillation under reduced pressure of from 5 to 200 mbar and at the prevailing temperature or an increased temperature of from 40.degree. to 140.degree. C., in order substantially to remove residual volatile components. The resins obtained are clear with little or no color and have a viscosity of preferably from 0.5 to 20 Pa.s (at 23.degree. C.) and a content of unreacted alcohol b) of preferably below 20% by weight, in particular below 10% by weight and especially below 5% by weight.
If desired the resin can also be diluted with solvent.
In addition to the aminotriazine derivative A) the binder of the invention comprises a radical polymer, polycondensation product or polyadduct B), which can be crosslinked with the aminotriazine derivative owing, for example, to its content of active hydrogen atoms (OH, NH and/or SH groups).
Suitable examples of component B) are alkyd resins, polyester resins, epoxy resins, polyurethane resins, and radical polymers based on acrylates, vinyl esters, dienes and aromatic vinyl compounds, or mixtures thereof.
Preference is given to radical polymers, polycondensation products or polyadducts containing OH groups, preferably having a hydroxyl number of from 20 to 200 mg of KOH/g of solids (in accordance with DIN 53240).
The binders according to the invention may for example contain from 1 to 99% by weight, preferably from 1 to 40% by weight and particularly preferably from 5 to 30% by weight of the aminotriazine derivatives A) and from 1 to 99% by weight, preferably from 60 to 99% by weight and particularly preferably from 70 to 95% by weight of component B), based on the sum of A) and B).
Examples of the form in which the binders may be present are solutions in water or organic solvents, or aqueous dispersions.
Additives which are conventional for the particular use intended may be added to the binders, examples of such additives being Theological auxiliaries, leveling agents, antifoams, pigments, dyes, etc.
The binders are particularly suitable for coating materials, especially as coating binders.
In this context they are suitable for a wide variety of substrates, such as glass, plastics, metal or wood.
The coating materials may be applied by the conventional methods, for example by brushing, dipping, rolling, knifecoating or spraying.
The binders according to the invention are distinguished by a high crosslinking reactivity which permits markedly shorter reaction times both on thermal curing (stoving enamels) and in the case of acid catalysis (acid-curing coating materials) in comparison with known, fully alkylated amino resins as have been employed, for example, as the starting material for the transetherification.
Suitable catalysts for the acid catalysis are, for example, strong acids such as sulfonic acids (e.g. para-toluenesulfonic acid, naphthalenesulfonic acid, etc.), phosphoric acid or derivatives of phosphoric acid, hydrochloric acid or other mineral acids. Metal salts such as zinc nitrate can also be employed, as can amine salts of the abovementioned acids, for example of p-toluenesulfonic acid with triethanolamine; it is also possible to add the components individually or to use commercial amine salts such as Nacure.RTM. grades.
The aminotriazine derivatives of the invention are particularly suitable in addition as sole binders for the coating, for example, of veneer finishing strips on furniture. For this purpose they may contain the abovementioned additives, but especially plasticizers and catalysts, for example polyalkylene glycols and arylsulfonic acids, for the curing operation, which is conventionally carried out at high temperatures.
EXAMPLES
All percentages are by weight unless specified otherwise.
The commercially available hexamethoxymethylmelamine (HMMM) resins, which are generally employed as precursors, constitute mixtures of different compounds, some of them including two or more melamine moieties. For this reason they are liquid at below 46.degree. C., which is the melting point of HMMM. Of course it is also possible to use pure crystalline HMMM as starting material, and the transacetalization generally leads to liquid products. In calculating the reaction mixtures an average molar mass of 390 g/mol--the molar mass of HMMM--was assumed for the HMMM resins used.
The glycol ethers are also subject to molecular weight distributions, especially when the number of ethylene oxide units is relatively high. Here too the molecular weight is calculated from the average number of ethylene oxide units incorporated.
The catalyst, p-toluenesulfonic acid, is always employed in the form of the monohydrate having a molar mass of 190.22 g/mol.
1. Methods of testing and analysis
Free formaldehyde
Determined by the titrimetric sulfite method according to DIN 16746-A.
Total formaldehyde
Determined titrimetrically after acid digestion.
Alcohol and glycol ether, free
Determined by gas chromatography.
Alcohol, bonded
Determined from the difference between the total alcohol content found by gas chromatography after acid digestion, and the content of free alcohol.
Nonvolatile components/solids content
In a method based on DIN 53216 2 g of resin and 2 g of butanol are weighed on a metal sheet intended for determining the content of dry matter and are baked in a convection oven at 125.degree. C. for two hours and then weighed again to calculate the nonvolatile fraction in % by weight (baking residue).
Viscosity
The viscosity of the resins is determined using a plate/cone viscometer: VISKO-PLOT from Epprecht Instruments and Controls AG, CH5606 Dottikon.
2 Transacetalization products
General preparation procedure for Examples 1 to 16
In an apparatus which is suitable for vacuum distillation and fitted with stirrer, condenser and distillation receiver, the quantity of glycol ether indicated in the examples of Table 1, with or without further high-boiling alcohols and with the stated amount of ptoluenesulfonic acid (pTSA) as catalyst are added to 1.5 mol of a hexamethoxymethylmelamine resin, and the mixture is heated to the temperature indicated. After it has reached this temperature distillation is carried out for one hour at the pressure indicated, and the batch is neutralized with a quantity of tributylamine which is equivalent to the quantity of acid employed. After the neutralization the batch is heated to 110.degree. C. and then distilled for 15 minutes at reduced pressure, diluted if appropriate with the quantity of 1-methoxy-2-propanol indicated, and cooled to room temperature. After filtration the resins obtained are clear and colorless or pale yellow, and are stable for at least 6 months: that is, they exhibit no phase separation and remain able to be processed. The analytical data are compiled in Table 2.
TABLE 1__________________________________________________________________________ Reaction Quantity conditions 1-Methoxy-2- pTSA rel. toEx. employed Temp. Pressure propanol initial charge YieldNo. Glycol ether �g! �mol! �.degree.C.! �mbar! �g! �mol %! �g! �%!__________________________________________________________________________1 Diethylene glycol monomethyl ether 18 0.15 82 30 30 1.36 598 1002 Diethylene glycol monomethyl ether 90 0.75 86 25 -- 1.36 631 973 Diethylene glycol monomethyl ether 180 1.50 83 40 -- 1.39 692 974 Triethylene glycol monomethyl ether 123 0.75 87 48 -- 1.37 663 975 Triethylene glycol monomethyl ether 247 1.50 88 50 -- 1.42 765 986 Tetraethylene glycol monomethyl ether 156 0.75 91 20 -- 1.36 698 977 Tetraethylene glycol monomethyl ether 312 1.59 88 27 -- 1.35 837 999 Diethylene glycol monobutyl ether 24 0.15 83 32 35 1.36 605 1009 Diethylene glycol monobutyl ether 61 0.38 83 35 -- 1.36 607 9610 Diethylene glycol monobutyl ether 122 0.75 86 26 -- 1.36 659 9611 Triethylene glycol monobutyl ether 155 0.75 90 23 -- 1.39 696 9512 Methylpolyglycol*) 78 0.15 88 35 -- 1.40 625 9513 Methylpolyglycol 390 0.75 81 42 -- 1.74 919 9714 Methylpolyglycol 780 1.51 93 40 -- 1.45 1283 9715 Lutensol .RTM. AO 3**) 780 2.25 91 53 -- 1.36 1258 9716 Lutensol AO 7**) 1176 2.25 91 62 -- 2.61 1656 98__________________________________________________________________________ *) R.sup.1 = CH.sub.3, n = 11 **) Oxo alcohol with 3 or 7 ether qroups
TABLE 2__________________________________________________________________________ Baking residue Viscosity at 23.degree. C. Methanol, free Glycol ether, freeExample No. �% by wt.! �Pa*s! �% by wt.! �% by wt.!__________________________________________________________________________1 88.8 5.3 2.2 0.12 88.9 5.6 0.8 0.33 87.9 3.2 0.5 0.64 90.3 5.7 0.6 0.35 87.8 2.2 0.7 0.46 89.6 3.8 0.4 0.27 86.2 1.3 0.7 0.58 87.0 5.4 1.4 <0.19 90.5 10.2 0.5 <0.110 90.7 3.5 0.5 0.311 92.9 5.4 0.5 <0.112 92.6 15.0 0.7 --13 90.2 2.0 0.2 --14 90.3 0.7 <0.1 --15 93.0 0.6 0.2 --16 91.3 0.3 <0.1 --__________________________________________________________________________
General Preparation Procedure for Examples 17 to 20 and for Comparison Example 1
1.5 mol of a hexamethoxymethylmelamine resin are placed in an apparatus which is suitable for vacuum distillation and is provided with stirrer, condenser and distillation receiver, and 0.25 mol of diethylene glycol monomethyl ether is added per mole of melamine in the starting material. The quantity of the acid catalyst stated in the Examples is added and the mixture is heated to 85.degree. C. . After reduction of the pressure to 15 mbar, volatile constituents are distilled off for one hour and the batch is then neutralized with a quantity of triethanolamine which is equivalent to the quantity of acid employed. Distillation is repeated for 15 minutes at 110.degree. C. and 15 mbar, the stated quantity of butyl glycol is added as diluent if appropriate, and the batch is cooled to room temperature. The resins obtained after filtration are clear and colorless or pale yellow, and have the analytical characteristics indicated in Table 3.
TABLE 3__________________________________________________________________________ Glycol Quantity monoether, �mol % in Methanol, free rel. to Butyl Baking Viscosity free �% ofExample initial glycol Yield residue at 23.degree. C. �% by quantityNo. Acid catalyst �g! charge! �g! �g! �% by wt.! �Pa .multidot. s! wt.! employed!__________________________________________________________________________17 Oxalic acid 0.59 0.31 -- 512 94.2 4.0 0.3 6.6 dihydrate18 Boron 0.92 0.21 -- 510 94.7 7.7 0.3 2.6 trifluoride etherate, 48%19 p-Toluene- 1.75 0.62 30 530 87.4 4.3 0.8 1.4 sulfonic acid20 Nitric acid 30% 1.96 0.62 30 530 93.5 5.1 0.1 1.4Comparison Acetic acid 0.56 0.62 -- 527 88 1.0 <0.1 93.2Example 1__________________________________________________________________________
Example 21
In a reactor with stirrer, condenser and distillation receiver, 460 g of the hexamethoxymethylmelamine resin Cymel 303 are mixed with 36 g of diethylene glycol monomethyl ether and 2.80 g of p-toluenesulfonic acid and the mixture is heated to 85.degree. C. Volatile components are removed by distillation for one hour at this temperature and at a pressure of 25 mbar. Following neutralization with tributylamine the distillation is continued for a further 15 minutes at 100.degree. C. and 25 mbar. After dilution with 35 ml of methoxypropanol and filtration 490 g of a clear, colorless resin are obtained which gives a baking residue of 89.8% and has a viscosity of 4.3 Pa.s at 23.degree. C.
The resin contains 0.3% of free methanol, and the conversion of diethylene glycol monomethyl ether is 96%.
Example 22
514 g of hexabutoxymethylmelamine are mixed with 0.5 mol of tetraethylene glycol monomethyl ether per dole of melamine and with 0.5% by weight of p-toluenesulfonic acid and the mixture is heated to 90.degree. C. Volatile components and reaction products are distilled off for 60 minutes at 30 mbar and 90.degree. C. Following neutralization with triethanolamine distillation is continued for a further 15 minutes at reduced pressure and 110.degree. C. After cooling and filtration a clear colorless resin is obtained in a yield of 95% which has a viscosity of 4.5 Pa.s at 23.degree. C.
Example 23
The volatile components and reaction products are distilled off over 60 minutes at 30 mbar and 90.degree. C. from a mixture of 1.6 mol (based on melamine) of a hexabutoxymethylmelamine resin with 164 g of diethylene glycol monobutyl ether and 0.5% by weight of p-toluenesulfonic acid. Distillation is continued at 25 mbar and 110.degree. C., after neutralization with methyldiethanolamine, for 15 minutes. After cooling and filtration the viscosity of the clear colorless resin is 4.0 Pa.s.
Comparison Example 2
In analogy to Example 1 in DE-C 24 14 426, 700 g of a hexamethoxymethylmelamine were dissolved in 1520 g of ethylene glycol monomethyl ether in a reactor with stirrer, condenser and distillation receiver. 28 g of 65% strength nitric acid were added and the mixture was stirred at 35.degree. C. for 35 minutes. After neutralization with 25 g of 50% strength sodium hydroxide solution a pH of 8.5 was established. The solution was concentrated at a temperature of 85.degree. C. and a pressure of from 90 to 130 mbar over the course of 2.5 hours. The pressure was reduced to 30 mbar and the distillation was continued for a further 30 minutes. After removal of the precipitated sodium nitrate by filtration, 940 g of a colorless, clear resin were obtained which had a viscosity of 650 means at 23.degree. C. It was impossible to detect free methanol, and the content of free ethylene glycol monomethyl ether was 15.5%.
General Preparation Procedure for Examples 24 to 28
468 g of a hexamethoxymethylmelamine resin were mixed with one mole of tetraethylene glycol monomethyl ether per mole of melamine in the HMMM resin and 1.5 mol % of p-toluenesulfonic acid. The alcohol listed in Table 4, in the quantity given there, is added and the mixture is heated to 85.degree. C. After reaching this temperature the pressure is reduced to 20 mbar and then volatile components are distilled off for 80 minutes. The mixture is cooled to 60.degree. C., neutralized with tributylamine, heated to 110.degree. C. and distilled under reduced pressure for a further 20 minutes. After cooling and filtration clear, colorless resins are obtained in yields of more than 95%, which resins have the analytical data indicated in Table
TABLE 4__________________________________________________________________________ Quantity Baking ViscosityEx. employed residue at 23.degree. C. Methanol, free TGMM.sup.a), freeNo. Alcohol �g! �% by wt.! �mPa .multidot. s! �% by wt.! �%! Alcohol.sup.b),__________________________________________________________________________ free24 Cyclohexanol 249.9 84 2.080 1.0 0.6 0.125 2-Ethythexanol 78.1 66 1.240 0.9 0.3 0.926 Lauryl alcohol 111.8 88 960 0.5 0.6 <1.427 Benzyl alcohol 259.5 83 2.000 0.8 1.0 1.028 1,4-Butanediolmono- 195.5 91 1.760 0.3 1.6 0.8 acrylate__________________________________________________________________________ .sup.a) Percentage of tetraethylene glycol monomethyl ether in the end product based on quantity of TGMM employed. .sup.b) Percentage of the alcohol of column 2 in the end product based on the quantity employed (column 3).
3. Coating formulations
General Preparation Procedure for an Acid-curing Coating Material
70 g of Alftalat AR (alkyd resin) 300 (60 percent), 20 g of the melamine-formaldehyde (MF) resin specified in the Examples (95% by weight) and 52 g of ethanol/1-methoxy-2-propanol (2:1) are stirred together with a spatula. Eased on the MF resin, 12% by weight of p-toluenesulfonic acid (20% strength solution in ethanol) are added to the coating material as curing agent. The coating material prepared in this way has a solids content of about 40% by weight. Alftalat AR 300 and melamine resin are present in the binder mixture in a ratio of 7:3.
General Preparation Procedure for the Solvent-containing White-pigmented Stoving Enamel
Pigment Paste
1200 g of the titanium dioxide pigment Kronos RN 57, 1000 g of the alkyd resin binder Alkydal R 40 (60 percent in xylene) and 200 g of methoxypropanol are dispersed twice on a hopper mill to give a uniform paste.
Paint Formulation
30 g of the above-described pigment paste, 22.5 g of the alkyd resin Alkydal R40, and a quantity of the MF resin listed in the Examples which corresponds to 9.0 g of solid resin, are stirred together with a spatula. Alkydal R40 and MP resin are present in the binder mixture in a ratio of 7:3, and there is twice as much binder as pigment (solvent:binder:pigment 2:2:1).
General Preparation Procedure for a Solvent-containing Clearcoat
A clearcoat is prepared by stirring together 50 g of an OH-containing polyacrylate (Luprenal.RTM. 240 S) having an OH number of 65 and a solids content of 60% by weight and 20 g of melamine resin, based on the solids content of the melamine resins specified in the Examples, and a quantity of a hydrocarbon (Solvesso.RTM. 100) which is sufficient for a solids content of 50% by weight. 0.5% by weight of p-toluenesulfonic acid may be added to the coating material to accelerate curing.
4. Testing of coatings
In order to emphasize the performance advantage of the binders or amino resins according to the invention, each coatings test employed as comparison material a commercially available hexamethoxymethylmelamine resin (HMMM comp.) as was employed as starting material in some of the preceding Examples, which resin has the following analytical characteristics:
______________________________________Solids content 93-96%Viscosity (23.degree. C.) 2000-6000 mPa .multidot. sFree formaldehyde <0.5%Methanol, attached >5 mol/mol of melamineFormaldehyde, attached >5.5 mol/mol of melamine______________________________________
In order to provide comparability, within each series resins according to the invention and the standard resin were processed and tested under comparable conditions.
General Procedure for Testing the Baking Reactivity
6 Glass plates (90.times.150.times.2 mm) are coated using a 150 .mu.m film-drawing frame with the solvent-containing white-pigmented coating material prepared by the above procedure and containing the amino resin specified in the Examples which follow, while 6 glass plates were coated with an identical coating material containing the commercial comparison resin instead of the amino resin of the invention, and the coatings were cured alongside one another in a drying cabinet at constant temperature. One glass plate each of the comparison and of the sample are removed after 10, 20, 30, 40, 50 and 60 min and, after being allowed to cool for at least ten minutes, the pendulum hardness is determined in accordance with DIN 53157.
General Procedure for Testing the Acid Curing (Kempf Test)
A 100 .mu.m film-drawing frame is used to coat a 380.times.67.times.3 mm glass plate with the acid-curing coating material prepared by the above procedure. After storage for five minutes in a convection oven at 40.degree. C. followed by storage for five minutes at room temperature the progress of the curing reaction is determined on the basis of the decrease in tack of the surface, using a Kempf chalking rate tester (supplier: Erichsen GmbH & Co. KG, S870 Hemer-Sundwig/Westphalia). In this test the tack is assessed by comparison with a scale (rating 5=highly tacky, rating 0=tack-free). The curing and testing cycle is carried out a total of six times.
General Procedure for the Gradient Oven Test
The stoving enamel is coated using a 200 .mu.m film-drawing frame onto a 567.times.90.times.0.75 mm deep-drawn metal panel, flushed off for 10 minutes and baked in a gradient oven, Byk type 2612, for 30 minutes over a temperature range from 80.degree. C. to 180.degree. C. After storage for 24 hours at 50% relative atmospheric humidity and 23.degree. C. the following tests are carried out in succession in the individual temperature zones:
The coating thickness is determined using a Deltascope coating thickness meter from Fischer, 7032 Sindelfingen.
The pendulum hardness is determined in accordance with DIN 53157 using a Byk instrument type 5840.
The crosshatch test is carried out in accordance with DIN 53151 using a crosshatching blade and adhesive tape.
The Erichsen indentation is determined in accordance with DIN 53156 using a Byk instrument type 5313.
The xylene resistance is determined by storage of one side of the panel, standing on its long side, to a depth of about 3 cm in a xylene bath for 10 minutes, and is then assessed: 1=no change in the coating film, 0.5=slight damage by scratching with the fingernail, 0=the coating film can be detached by rubbing with a cloth.
Test Results
White-pigmented solvent-containing stoving enamels and acid-curing coating materials were prepared by the general preparation procedure, using the MP resins listed in Tables 5 and 6. The pendulum hardnesses after baking at 150.degree. C. are indicated in Table 5. The results of acid curing (Kempf tests) are compiled in Table 6.
TABLE 5__________________________________________________________________________Pendulum hardness (seconds) after after after after after afterMF resins from Ex. No. 10 min 20 min 30 min 40 min 50 min 60 min__________________________________________________________________________3 36 97 133 154 167 1725 35 83 126 153 162 1717 35 85 118 134 158 1618 57 91 122 143 158 16812 56 116 129 148 158 16520 14 44 71 78 83 9121 63 94 110 116 130 137Comparison Example 1 8 23 37 43 53 58Comparison Example 2 7 10 27 30 36 40HMMM Comp. 10 30 44 58 71 82__________________________________________________________________________
The high values for the pendulum hardness where MF resins from the Examples are used rather than those from the Comparison Examples or HMMM emphasize the high reactivity. The increased reactivity in acid curing is documented by the rapid attainment of a tack-free film.
TABLE 6__________________________________________________________________________Kempf test (rating)Amino resin from 1 2 3 4 5 6Example No. Cycle Cycles Cycles Cycles Cycles Cycles__________________________________________________________________________3 0-1 0 -- -- -- --5 1-2 1 0-1 0-1 0 --7 1-2 0-1 0-1 0 -- --9 1 0-1 0 -- -- --12 1 0-1 0 -- -- --20 0-1 0-1 0 -- -- --21 1 0-1 0-1 0 -- --Comparison Example 1 5 5 4 4 3-4 3-4Ccmparison Example 2 3-4 2 1-2 0 -- --HMMM Comp. 5 3-4 2-3 1-2 1 0-1__________________________________________________________________________
Using the amino resins of the invention from Examples 24, 27 and 28, and the comparison HMMM resin, acid-curing clearcoats and solvent-containing white-pigmented coating materials are prepared for testing the baking reactivity, and are processed and tested in accordance with the general procedures for plotting the curing curve and for testing the acid curing. The results of the thermal curing and of the acid curing are compiled in Tables 7 and
TABLE 7__________________________________________________________________________Pendulum hardness (seconds) after after after after after afterMF resin from Example No. 10 min 20 min 30 min 40 min 50 min 60 min__________________________________________________________________________24 25 67 73 99 122 13627 12 43 88 99 130 14428 15 97 139 157 162 171HMMM comp. 0 23 35 58 74 92__________________________________________________________________________
TABLE 8______________________________________Kempf test (rating)MF resin from 1 2 3 4 5 6Example No. Cycle Cycles Cycles Cycles Cycles Cycles______________________________________24 3 1 0-1 0 -- --27 2 1-2 1 0-1 0 --28 4 1-2 0-1 0 -- --HMMM comp. 4-5 3-4 2 1-2 0-1 0______________________________________
White-pigmented solvent-containing stoving enamels were prepared in accordance with the general procedure given above using the MF resins from Examples 2, 6 and 9 and using a HMMM comparison.
The coating materials prepared in this way were knife-coated onto deep-drawn metal panels and, in accordance with the general procedure, were baked in a gradient oven and tested. The test results are compiled in Tables 9 and 10.
The high values for the pendulum hardness at relatively low baking temperatures (Table 9) emphasize the high reactivity, as does the attainment of a xylene-resistant film at below 180.degree. C. (Table 10).
TABLE 9__________________________________________________________________________ Temerature �.degree.C.!MF resin from Example No. Parameter 100 110 120 130 140 150 160 170 180__________________________________________________________________________ Coating thickness2 �.mu.m! 44 48 47 46 50 51 51 52 476 46 46 48 47 52 49 48 50 529 47 50 48 51 50 48 48 46 48HMMM Comp. 42 44 40 44 46 47 45 45 48 Pendulum hardneas2 (Number of swings) 8 19 48 88 105 116 124 132 1416 8 19 42 78 94 108 124 129 1109 8 16 41 76 101 111 124 136 110HMMM Comp. 8 8 11 16 27 42 76 109 106 Erichsen indentation2 �mm! 9.0 9.0 9.0 7.9 6.6 7.0 5.8 2.5 4.76 9.0 9.0 9.0 8.2 7.7 5.4 3.7 2.5 1.59 9.0 9.0 9.0 8.2 7.5 6.8 4.4 4.3 4.7HMMM Comp. 9.0 9.0 9.0 9.0 9.0 9.0 9.0 8.0 9.0__________________________________________________________________________
TABLE 10______________________________________ Xylene-resistantExample No. �.degree.C.!______________________________________2 1506 1509 150HMMM Comp. 7 >180______________________________________ The coating is resistant to xylene above the indicated temperature.
The amino resin of Example 19 according to the invention and a HMMM comparison resin were used to prepare solvent-containing clearcoats and an acid-catalyzed solvent-containing clearcoat in accordance with the general procedure. The coating materials prepared in this way were knife-coated onto deep-drawn metal panels, baked in a gradient oven in accordance with the general procedure and tested. The test results are compiled in Tables 11 and 12 and indicate, via the rapid rise in pendulum hardness and the low-temperature attainment of resistance to water and xylene, the high reactivity of the melamine-formaldehyde resins according to the invention, which can be increased further by acid catalysis.
TABLE 11__________________________________________________________________________MF resin Temperaturefrom Ex. �.degree.C.!No. Parameter 100 110 120 130 140 150 160 170 180__________________________________________________________________________ Coating thickness19 �.mu.m! 28 34 36 37 37 39 36 35 34withoutpTSA19 with 35 37 38 39 38 36 36 35 34pTSAHMMM --.sup.a) -- 28 29 33 33 30 31 32comp. Pendulum attenuation19 �Number of 4 11 19 29 41 63 81 97 102without swings!pTSA19 with 40 56 68 80 87 95 96 102 103pTSAHMMM -- -- -- -- -- -- 12 44 82comp.__________________________________________________________________________
TABLE 12______________________________________ The coating is The coating isMF resin from Ex. resistant to xylene resistant to waterNo. above above______________________________________19 without pTSA 180.degree. C. 120.degree. C.19 with pTSA 160.degree. C. 120.degree. C.HMMM comp. >190.degree. C. 170.degree. C.______________________________________
a) impossible to determine owing to insufficient curing of coating

Number	Date	Country
A 0 062 179	Oct 1982	EPX
A 0 262 518	Apr 1988	EPX
A 2 307 806	Nov 1976	FRX
A-24 14 426	Oct 1975	DEX
36 32 587	Apr 1988	DEX

Aminotriazine derivatives containing glycol ether and their use in coating resins

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