Detergent composition
A technology of composition and cleaning agent, which is applied in the direction of detergent composition, surface active detergent composition, bleaching agent of washing composition, etc., which can solve the problems of reduced cleaning power, device failure, foam overflow, etc., and achieve high cleaning power Effect
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manufacture example 1
[0178] (Manufacture example 1) Manufacture of (A-1)
[0179] As a nonionic surfactant, a polyoxyalkylene alkyl ether having 1 to 400 oxyalkylene groups and having a hydroxyl group at the end of the oxyalkylene group (manufactured by ADEKA Corporation, ADEKANOLB722) (140 g) 20 g of dihydropyran (DHP) and 1 mol% p-toluenesulfonic acid as a catalyst were added to a dichloromethane solution (50 ml) of , and stirred overnight (10 hours) at room temperature. Sodium bicarbonate was added to complete the reaction, and after filtration, the solvent was distilled off to obtain the target product.
[0180] The obtained product is the nonionic surfactant (A-1) which the terminal hydroxyl group of the said nonionic surfactant reacted with DHP, and which has an acetal structure at the terminal.
manufacture example 2
[0181] (Manufacture example 2) Manufacture of (A-2)
[0182] As a nonionic surfactant, polyoxyalkylene alkyl ethers (manufactured by ADEKA Co., Ltd., ADEKANOLBO-922) ( 110 g) of dichloromethane solution (50 ml) were added with 18 g of ethyl vinyl ether and 1 mol% p-toluenesulfonic acid as a catalyst, and stirred at room temperature overnight (10 hours). Sodium bicarbonate was added to complete the reaction, and after filtration, the solvent was distilled off to obtain the target product.
[0183] The obtained product is the nonionic surfactant (A-2) which the terminal hydroxyl group of the said nonionic surfactant reacted with ethyl vinyl ether, and which has an acetal structure at the terminal.
manufacture example 3
[0184] (Manufacture example 3) Manufacture of (A-3)
[0185] As a nonionic surfactant, a polyoxyalkylene alkyl ether (manufactured by ADEKA Corporation, ADEKANOLB-2020) having an oxyalkylene group in the range of 1 to 400 and having a hydroxyl group at the end of the oxyalkylene group ( 17 g of 2,3-dihydrofuran and 1 mol% p-toluenesulfonic acid as a catalyst were added to a dichloromethane solution (50 ml) of 300 g) and stirred at room temperature overnight (10 hours). Sodium bicarbonate was added to complete the reaction, and after filtration, the solvent was distilled off to obtain the target product.
[0186] The obtained product is the nonionic surfactant (A-3) which reacted the terminal hydroxyl group of the said nonionic surfactant, and 2, 3- dihydrofuran, and has an acetal structure in the terminal.
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