Levelling agent for surface paint
A technology of surface coating and leveling agent, applied in the field of leveling agent, can solve the problems of high viscosity of leveling agent, inappropriate solution, difficult handling by users, etc.
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Embodiment 1
[0045] In a glass flask equipped with a stirrer, thermometer, distillation unit, dropping funnel and nitrogen gas inlet tube, 3.9 g of macromonomer (macromonomer 12, see Example, which is composed of a Acryloyl, poly(2-ethylhexyl acrylate-ethyl acrylate) with a molecular weight of 5500) and 86.7 g of toluene. Nitrogen was passed through the mixture throughout the reaction. After the reaction temperature had been raised to 90 °C, a mixture of 0.92 g of AIBN, 119.6 g of 2-ethylhexyl acrylate and 6.5 g of benzyl methacrylate was added at a uniform rate over the course of 150 minutes , metered into it. After the addition step was complete, the reaction mixture was maintained at 90°C for 120 minutes. After this period of time has elapsed, the nitrogen feed is stopped and the reaction temperature is raised to 150° C. while applying vacuum (<25 mbar). Solvents, initiator decomposition products and monomer residues are distilled off until the non-volatile content is greater than 99...
Embodiment 24
[0082] 30 g of the polymer described in Example 9 (hydroxyl number approximately 65) was charged together with 4.6 g of acetic anhydride into a four necked flask equipped with a stirrer, thermometer, reflux condenser and nitrogen inlet. Nitrogen was passed through the mixture throughout the reaction. Under stirring, the reaction temperature was increased to 75° C., and stirring was continued for 2 hours. After this time, free hydroxyl groups are no longer detectable in the IR spectrum. The nitrogen supply was stopped and the reaction temperature was raised to 150°C while applying vacuum (<25 mbar). Free acetic acid and excess acetic anhydride are distilled off until the non-volatile content is greater than 99%. A polymer having a pale yellow color was obtained. Example 25: Reaction of the inventive polymer of Example 9 with an isocyanate to form a secondary carbamate
Embodiment 25
[0083] 30 g of the polymer described in Example 9 (the number of hydroxyl groups is about 65) and 30 g of butyl acetate together with 0.03 g of DBTL solution (concentration in xylene is 10%) are charged into a Thermometer, reflux condenser, dropping funnel and nitrogen inlet tube in a four-necked flask. Nitrogen was passed through the mixture throughout the reaction. With stirring, the reaction temperature was raised to 60° C. and 4.4 g of hexyl isocyanate were metered in dropwise over the course of 10 minutes. An exothermic reaction ensues. After 90 minutes, the isocyanate groups were no longer detectable in the IR spectrum. The nitrogen supply was stopped and the reaction temperature was raised to 150°C while applying vacuum (<25 mbar). Butyl acetate is distilled off until the non-volatile content is greater than 99%. A polymer having a pale yellow color was obtained. Example 26: Reaction of the inventive polymer of Example 9 with maleic anhydride to form a maleic acid ...
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