Fast curing alkoxysilane spray foam
An alkoxysilane, multi-component technology, which is used in drug combinations, bandages, transportation and packaging, etc., can solve the problems of citric acid caustic or corrosive application range limitations, foam difficulties, etc.
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Embodiment 1
[0146] Example 1: Preparation of silane-terminated prepolymer STP1
[0147] The mixture of 1000g HDI and 1g benzoyl chloride was added dropwise and mixed with 1000g of polyalkylene oxide with a molar mass of 4680 g / mol at 80°C within 3 hours, and stirred for 12 hours after the dropwise addition, wherein the polyalkylene oxide was composed of Glycerol was initially prepared with 71% by weight ethylene oxide and 26% by weight propylene oxide, pre-dried at 0.1 mabr pressure and 100°C for 6 hours. Excess HDI was removed by thin-film distillation at 130° C. and 0.1 mbar. This gave a prepolymer having an NCO content of 2.42% and a viscosity of 3500 mPas.
[0148] Then 200 g of the prepolymer obtained were mixed with 31.7 g of Geniosil XL 926 within 10 minutes at 30-40°C. After further stirring at 30 °C for 60 min, complete conversion of the NCO prepolymer to STP was detected by IR spectroscopy. This gave a viscous, colorless liquid.
Embodiment 2
[0149] Example 2: Preparation of silane-terminated prepolymer STP2
[0150] 390 g of Desmodur N 3300 were dropwise mixed with 1125 g of a polyalkylene oxide having a molar mass of 2250 g / mol at 80° C. and stirred at 80° C. until an NCO content of 3.67% was reached, wherein the polyalkylene oxide consisted of Butyl diglycol was initially prepared, and the weight fraction of ethylene oxide was 79% and the weight fraction of propylene oxide was 14%, and it was pre-dried at 100° C. for 2 hours under a pressure of 0.1 mabr.
[0151] Then 5.0 g of the prepolymer obtained were mixed with 1.2 g of Geniosil XL 926 within 10 minutes at room temperature. After a further 30 min of stirring, complete conversion of the NCO prepolymer to STP was detected by IR spectroscopy. This gave a viscous, colorless liquid.
Embodiment 3
[0152] Example 3: Preparation of silane-terminated prepolymer STP3
[0153] 490 g of Desmodur XP 2599 was mixed dropwise at 80° C. with 394 g of a polyalkylene oxide having a molar mass of 2250 g / mol, and after the dropwise addition was stirred at 80° C. until an NCO content of 2.22% was reached, wherein the polyalkylene oxide consisted of Butyl diglycol was initially prepared, and the weight fraction of ethylene oxide was 79% and the weight fraction of propylene oxide was 14%, and it was pre-dried at 100° C. for 2 hours under a pressure of 0.1 mabr.
[0154]A solution of 51.8 g of the prepolymer obtained in 70 g of dry diethyl ether was then mixed with 7.5 g of Geniosil XL 926 within 10 minutes at room temperature. After a further 30 min of stirring, complete conversion of the NCO prepolymer to STP was detected by IR spectroscopy. This gave a viscous, colorless liquid.
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Abstract
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Application Information
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