Water and oil repellent using α-chloroacrylate
A water-repellent, oil-repellent, and water-based medium technology, applied in the field of water-repellent and oil-repellent agents, can solve problems such as uneven treatment, reduced performance of treated objects, and reduced washing durability, achieving the effect of maintaining performance and excellent water repellency
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[0076] The present invention will be described more specifically with reference to Examples (Examples 1 to 10) and Comparative Examples (Comparative Examples 1 to 5), but the present invention is not limited to these.
[0077] Hereinafter, % is % by weight unless otherwise specified.
Synthetic example 1
[0079] Synthesis of Siloxane A:
[0080] Into a three-necked round-bottomed flask equipped with a cooler, upper stirrer and thermocouple were added silanol-terminated polydimethylsiloxane (743g, Mn about 300), mercaptopropylmethyldiethoxysilane (230g) , aminopropylmethyldiethoxysilane (27g), trimethylethoxysilane (39g), barium hydroxide (0.62g) and sodium orthophosphate (0.25g). The reaction mixture was heated to 75°C, maintained at this temperature for 3 hours, and then volatiles were removed for 4 hours at 75°C and a reduced pressure of 200 mbar.
[0081] The physical and structural properties of aminomercaptosiloxane are described below:
[0082]
Embodiment 1
[0084] Add 153.4g CF to a 1L autoclave 3 CF 2 -(CF 2 CF 2 ) n -CH 2 CH 2 OCOC(Cl)=CH 2 (n=2.0), 35.2g octadecyl acrylate, 4.8g glycerol monomethacrylate, 460g pure water, 78.2g tripropylene glycol, 9.8g polyoxyethylene lauryl ether (EO: 20 EO represents the number of vinyl oxide units), 3.9 g of polyoxyethylene isotridecyl ether (EO: 3), 2.0 g of polyoxyethylene oleyl ether (EO: 50), under stirring, at a temperature of 60 °C It was emulsified and dispersed by ultrasonic waves for 15 minutes. After the inside of the autoclave was replaced with nitrogen, 58.8 g of vinyl chloride was press-filled. A solution of 2.4 g of dodecyl mercaptan, 3.3 g of 2,2-azobis(2-amidinopropane) dihydrochloride (hereinafter referred to as V-50) and 20 g of water was added, and the reaction was carried out at 60°C. After 5 hours, an aqueous dispersion of the polymer was obtained. The polymer composition was approximately the same as that of the added monomers.
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