Process for preparing composite modified aqueous polyurethane emulsion
A water-based polyurethane and composite modification technology, which is applied in the field of preparation of composite modified water-based polyurethane emulsion, can solve the problem that the hardness and application performance requirements are not suitable, the water-based polyurethane is not strong in water resistance, and the substrate adhesion is not strong enough. and other problems, to achieve the effect of suitable application performance requirements, good water resistance and convenient operation.
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Embodiment 1
[0031] Synthesis method:
[0032] 100g of diisocyanate (HDI) and 165g of polyoxypropylene diol (N 210 , Mw=1000±10) was added to the reaction tank with nitrogen gas, 2.5g of γ-aminopropyltriisooxysilane (KH-550) was added to the above reaction tank, and finally 25g of dimethylolpropane Acid (DMPA) was added to the reaction tank. After stirring the reaction at 70° C. for 5 h, 300 g of prepolymer were obtained.
[0033] 5g of triethylamine was dissolved in 168g of deionized water at 5°C. Add 100 g of the above-mentioned prepolymer to the triethylamine solution under stirring, and emulsify for 25 minutes with a high-speed shear emulsifier. .
[0034] Take this polyurethane emulsion 100g, add 2g of K 2 SiO 3 , reacted at 10°C for 4 hours to obtain an emulsion with a solid content of 36.7%, and the emulsion was formed into a film. The dry film was a high-gloss transparent film with a tensile strength of 19.3Mpa, an elongation at break of 485%, and a water absorption of 12.6%....
Embodiment 2
[0036] Synthesis method:
[0037] Mix 100g diisocyanate (TDI) with 250g polyoxypropylene diol (N 220 , Mw=2000±100) was added to the reaction tank with nitrogen gas, 18g aminoethylaminopropyl polydimethylsiloxane was added to the above reaction tank, and finally 5g of dimethylolpropionic acid ( DMPA) was added to the reaction tank. After stirring the reaction at 90° C. for 4.5 h, 373 g of prepolymer were obtained.
[0038] 2g of triethylamine was dissolved in 200g of deionized water at 2°C. Add 100 g of the above-mentioned prepolymer to the triethylamine solution under stirring, and emulsify for 25 minutes with a high-speed shear emulsifier.
[0039] Take this polyurethane emulsion 100g, add 0.8g K 2 SiO 3 , and reacted at 20°C for 3 hours to obtain a polyurethane emulsion with a solid content of 22.2%. The emulsion was formed into a film, and the dry film was a high-gloss transparent film with a tensile strength of 17.3Mpa, elongation at break of 460%, and water absorpti...
Embodiment 3
[0041] Synthesis method:
[0042] 100g of diisocyanate (MDI) and 300g of polyoxypropylene triol (N 330 , Mw=3000±100) was added to the reaction tank with nitrogen gas, 6.5gr-aminopropyltriisooxysilane (KH-550) was added to the above reaction tank, and finally 20g of dimethylolpropionic acid (DMPA) was added to the above reaction tank. The reaction was stirred at 100° C. for 3.0 h to obtain 426.5 g of prepolymer.
[0043] 4 g of triethylamine was dissolved in 162 g of deionized water at 10°C. Add 100 g of the above-mentioned prepolymer to the triethylamine solution under stirring, and emulsify for 25 minutes with a high-speed shear emulsifier.
[0044] Get this polyurethane emulsion 100g, add the colloidal aqueous solution (K 2 O content 7.0~9.0wt%, SiO 2 Content 19~29wt%), stirred and reacted at 18°C for 4h to obtain a polyurethane emulsion with a solid content of 45.6%. After film formation, the dry film was a high-gloss transparent film with a tensile strength of 19.3...
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