Preparation method of polysiloxane modified polyurethane water dispersion
A polyurethane water dispersion and polysiloxane technology, which is applied in the field of preparation of modified polyurethane materials, can solve the problems of lack of chemical crosslinking, poor mechanical properties of water-based polyurethane, water resistance, solvent resistance, heat resistance, and unsatisfactory gloss, etc. problem, to achieve the effect of good bending resistance and good water resistance
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Embodiment 1
[0023] Synthesis of prepolymer: In a three-necked flask equipped with a stirrer and a thermometer, 100 g of isophorone diisocyanate (IPDI) was added, and the temperature was raised until it melted. Then, add 1g of polyether 210 and polyether 220 that have been dehydrated, react at about 70°C for 30 minutes, add 3g of α-hydrogen-ω-hydroxyl-polydimethylsiloxane (M=1000), and react at the same temperature 30min. Then add 3.18g of dimethylolpropionic acid (dissolved in 10g N,N-dimethylformamide) into the reaction system, react at 70°C for 30min, then add 15g of ethylene glycol and react for 40min, take a sample, and use a standard The NCO content in the prepolymer was analyzed by di-n-butylamine back titration. When the isocyanate content reaches the set value (when the isocyanate content in the prepolymer reaches 40-80% of the initial value), the reaction is terminated to obtain an isocyanate group-terminated polyurethane prepolymer.
[0024] Preparation of aqueous dispersion: ...
Embodiment 2
[0030] Synthesis of prepolymer: In a three-necked flask equipped with a stirrer and a thermometer, 100 g of isophorone diisocyanate (IPDI) was added, and the temperature was raised until it melted. Then, add 3g of polyether 210 and polyether 220 that have been dehydrated, react at about 70°C for 30 minutes, add 5g of α-hydrogen-ω-hydroxyl-polydimethylsiloxane (M=2000), and react at the same temperature 30min. Then add 3.18g of dimethylolpropionic acid (dissolved in 10g N,N-dimethylformamide) into the reaction system, react at 70°C for 30min, then add 20g of ethylene glycol and react for 40min, take a sample, and use a standard The NCO content in the prepolymer was analyzed by di-n-butylamine back titration. When the isocyanate content reaches the set value (when the isocyanate content in the prepolymer reaches 40-80% of the initial value), the reaction is terminated to obtain an isocyanate group-terminated polyurethane prepolymer.
[0031] Preparation of aqueous dispersion: ...
Embodiment 3
[0036]The synthesis of prepolymer: in the there-necked flask that stirrer and thermometer are equipped with, add the isophorone diisocyanate (IPDI) of 100g, be heated to its fusing. Then, add 5g of polyether 210 and polyether 220 that have been dehydrated, react at about 70°C for 30 minutes, add 7g of α-hydrogen-ω-hydroxyl-polydimethylsiloxane (M=2000), and react at the same temperature 30min. Then add 3.18g of dimethylolpropionic acid (dissolved in 10g N,N-dimethylformamide) into the reaction system, react at 80°C for 25min, then add 25g of ethylene glycol and react for 40min, take a sample, and use a standard The NCO content in the prepolymer was analyzed by di-n-butylamine back titration. When the isocyanate content reaches the set value (when the isocyanate content in the prepolymer reaches 40-80% of the initial value), the reaction is terminated to obtain an isocyanate group-terminated polyurethane prepolymer.
[0037] Preparation of aqueous dispersion: cool the prepoly...
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