Coating agent comprising oligocarbonate for scratch-resistant finishing lacquer
An oligocarbonate, composition technology, applied in the direction of polyurea/polyurethane coatings, coatings, etc., can solve the problem of not giving detailed quantitative composition or molecular weight and OH functionality of polycarbonate polyol, low crosslinking density, high viscosity problem
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[0062] The preparation of the resin of component b) is carried out by copolymerization of components b1) to b7) according to conventional methods familiar to those skilled in the art [Houben-Weyl (eds.): Methods of Organic Chemistry, 4th edition, E20 / 2. Thieme, Stuttgart 1987, p. 1156], preference is given to free-radical solution polymerization of components b1) to b7) in the presence of free-radical initiators at temperatures from 140°C to 240°C.
[0063] The monomers and / or oligomers b1) to b7) are generally incorporated into the copolymer in the same proportions in which they were used for the polymerization. The distribution of binding units is essentially random.
[0064] Suitable base polymers b1) for the copolymer b) essential to the invention include in principle all polybutylene moieties having a number-average molecular weight of 500-10,000 g / mol and having ethylene double At least 10 mole percent, preferably at least 20 mole percent, more preferably at least 40 mo...
Embodiment 1
[0105] Preparation of aliphatic oligocarbonate diols with a number average molecular weight of 1000 g / mol based on 1,6-hexanediol
[0106] 2943 g of 1,6-hexanediol containing 0.7 g of ytterbium(III) acetylacetonate and 1051 g of dimethyl carbonate were charged at 80°C into a 5-liter pressure reactor with a distillation apparatus installed on top, a stirrer and a receiver ester. The reaction mixture was then heated to 150° C. under nitrogen atmosphere within 2 hours and kept at this temperature under reflux and stirring for 2 hours, the pressure was increased to 3.9 bar (absolute). The elimination product methanol was subsequently removed by distillation as a mixture with dimethyl carbonate, during which the pressure continued to drop by a total of 2.2 bar over the course of 4 hours. The distillation step was then terminated and a further 1051 g of dimethyl carbonate were pumped into the reaction mixture at 150° C., the reaction mixture was maintained at this temperature for 2...
Embodiment 2
[0109] Preparation of an aliphatic oligocarbonate diol with a number average molecular weight of 650 g / mol, based on 3-methyl-1,5-pentanediol
[0110] According to the steps of Example 1, the difference is that instead of 1,6-hexanediol, 34092 grams of 3-methyl-1,5-pentanediol and 8.0 grams of acetylene were added to the 60-liter autoclave at the beginning Ytterbium(III) acetone, and dimethyl carbonate was added in three steps, twice at 10223 grams and once at 7147 grams.
[0111] This gives a colorless liquid oligocarbonate diol having the following properties:
[0112] m n = 675 g / mol; OH number = 166.0 mg KOH / g; viscosity: 4146 mPas at 23°C.
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Abstract
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