Polyester Prepolymers
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example 1 (
According to the Invention)
[0065]In a 5 l sulfonating beaker with a lid, stirrer, thermometer and nitrogen flow, 0.6 g dibutyltin dilaurate (Desmorapid Z®, Bayer MaterialScience AG, Leverkusen, Del.) were added to 2197.92 g of the polyester diol A and the mixture was heated to 60° C. 814.3 g isocyanatopropyltrimethoxysilane (Geniosil® GF40, Wacker AG, Burghausen) were then added dropwise over three hours and stirring was continued until an NCO content could no longer be detected by titration. The alkoxysilyl end group-containing polyurethane prepolymer obtained had a viscosity of 6,450 mPas (23° C.).
example 2 (
According to the Invention)
[0066]In a 10 l reactor with a lid, stirrer, thermometer and nitrogen flow, 0.5 g dibutyltin dilaurate (Desmorapid Z®, Bayer MaterialScience AG, Leverkusen, Del.) were added to 4470.2 g of the polyester diol B and the mixture was heated to 60° C. 529.3 g isocyanatopropyltrimethoxysilane (Geniosil® GF40, Wacker AG, Burghausen) were then added dropwise over half an hour and stirring was continued until an NCO content could no longer be detected by titration. The alkoxysilyl end group-containing polyurethane prepolymer obtained had a viscosity of 90,500 mPas (23° C.).
example 3 (
According to the Invention)
[0067]In a 5 l sulfonating beaker with a lid, stirrer, thermometer and nitrogen flow, 0.2 g dibutyltin dilaurate (Desmorapid® Z, Bayer MaterialScience AG, Leverkusen, Del.) were added to 2387.2 g of the polyester diol A and the mixture was heated to 60° C. Next, 117.6 g hexamethylene diisocyanate (Desmodur H®, Bayer MaterialScience AG, Leverkusen, Del.) were added first over half an hour and 557.1 g isocyanatopropyltrimethoxysilane (Geniosil® GF40, Wacker AG, Burghausen) were then added dropwise over an hour and stirring was continued until an NCO content could no longer be detected by titration. The alkoxysilyl end group-containing polyurethane prepolymer obtained had a viscosity of 25,100 mPas (23° C.).
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