surface treatment agent
A technology of surface treatment agent and surfactant, applied in fiber treatment, other chemical processes, fiber repelling to liquid, etc., can solve the problem of poor water repellency and oil repellency of water repellent, and achieve excellent strong water repellency and excellent water repellency. Water repellency and oil repellency, good stability
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[0228] Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples. However, these descriptions do not limit the present invention.
[0229] Hereinafter, unless otherwise specified, parts, %, or ratios represent parts by weight, % by weight, or ratio by weight.
[0230] The procedure of the test is described below.
[0231] Bundesmann water repellency test
[0232] According to the method described in JIS L1092 (C) (Bundesmann test), the water repellency was evaluated by raining under the conditions of 80 cc / min of rainfall, 20° C. of rainwater temperature, and 5 minutes or 10 minutes of raining time. The water repellency is represented by 6 grades (0, 50, 70, 80, 90 and 100) from 0 to 100. A higher score indicates better water repellency. Grades marked with + (-) indicate that they are slightly better (worse) in quality.
manufacture example 1
[0234] In a 500mL autoclave, add stearyl acrylate=45g, isobornyl methacrylate=5g, pure water=145g, tripropylene glycol=15g, sorbitan monooleate=1.5g, polyoxygen Ethylene (EO: 18) secondary alkyl (C12-14) ether = 2 g, di-octadecyl dimethyl ammonium chloride = 1.5 g, ultrasonic emulsification and dispersion at 60° C. for 15 minutes while stirring. After substituting nitrogen in the autoclave, 2,2-azobis(2-amidinopropane) 2 hydrochloride=0.5 g was added, and it was made to react at 60 degreeC for 3 hours, and the aqueous dispersion liquid of the polymer was obtained. Further, the solid content concentration was adjusted to 30% with pure water. The monomer composition of the resulting polymer is basically the same as that of the added monomer.
manufacture example 2
[0236] Add stearyl acrylate=40g, isobornyl methacrylate=10g, pure water=145g, tripropylene glycol=15g, acetylene glycol polyoxyethylene adduct=1g, Polyoxyethylene (EO: 18) isotridecyl ether = 2 g, dioctadecyl dimethyl ammonium chloride = 2 g, and was dispersed by ultrasonic emulsification at 60° C. for 15 minutes while stirring. After substituting nitrogen in the autoclave, 2,2-azobis(2-amidinopropane) 2 hydrochloride=0.5 g was added, and it was made to react at 60 degreeC for 3 hours, and the aqueous dispersion liquid of the polymer was obtained. Further, the solid content concentration was adjusted to 30% with pure water. The monomer composition of the resulting polymer is basically the same as that of the added monomer. Manufacturing example 3
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