A kind of durable fabric waterproofing agent and preparation method thereof
A waterproofing agent and long-lasting technology, which is applied in the direction of plant fibers, textiles and papermaking, and liquid-repellent fibers, etc. It can solve the problems of poor waterproof effect, rearrangement of molecular conformation, poor waterproof effect, etc., and achieve durable waterproof effect , low surface energy, suitable for industrial production and popularization and application
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Embodiment 1
[0044] 1. Preparation of trifluorooctyl p-acryloyloxybenzoate functional monomer
[0045] In a three-necked flask equipped with magnetic stirring, water separation device, reflux condenser and thermometer, add 4.15 grams of p-hydroxybenzoic acid, 11.01 grams of tridecafluorooctyl alcohol, 0.8 grams of p-toluenesulfonic acid and 100 grams of xylene in sequence, and heat to 130° C., and reacted in a nitrogen atmosphere for 12 hours. After the reaction, the reaction solution was cooled to room temperature (20°C), filtered with suction, washed with hot water at 70°C, and dried (placed in a vacuum drying oven at a temperature of 50°C) to obtain a white solid The intermediate product of trifluorooctyl p-hydroxybenzoate.
[0046] In a three-necked flask equipped with a magnetic stirrer, a thermometer, a constant pressure dropping funnel, and a reflux condenser, add 20 grams of dichloromethane, 1.21 grams of triethylamine, and 4.84 grams of trifluorooctyl p-hydroxybenzoate in sequence,...
Embodiment 2
[0060] 1. Preparation of trifluorooctyl p-acryloyloxybenzoate functional monomer
[0061] In a three-necked flask equipped with magnetic stirring, water separation device, reflux condenser and thermometer, add 4.0 grams of p-hydroxybenzoic acid, 11.0 grams of tridecafluorooctyl alcohol, 0.7 grams of p-toluenesulfonic acid and 98 grams of xylene in sequence, and heat to 130° C., and reacted in a nitrogen atmosphere for 12 hours. After the reaction, the reaction solution was cooled to room temperature (20°C), filtered with suction, washed with hot water at 70°C, and dried (placed in a vacuum drying oven at a temperature of 50°C) to obtain a white solid The intermediate product of trifluorooctyl p-hydroxybenzoate.
[0062] In a three-necked flask equipped with magnetic stirring, a thermometer, a constant pressure dropping funnel, and a reflux condenser, add 18 grams of dichloromethane, 1.21 grams of triethylamine, and 4.84 grams of tridefluorooctyl p-hydroxybenzoate in sequence,...
Embodiment 3
[0070] 1. Preparation of trifluorooctyl p-acryloyloxybenzoate functional monomer
[0071] In a three-necked flask equipped with magnetic stirring, water separation device, reflux condenser and thermometer, add 4.2 grams of p-hydroxybenzoic acid, 11.3 grams of tridecafluorooctyl alcohol, 0.9 grams of p-toluenesulfonic acid and 102 grams of xylene in sequence, and heat to 150° C., and reacted in a nitrogen atmosphere for 24 hours. After the reaction, the reaction solution was cooled to room temperature (20°C), filtered with suction, washed with hot water at 70°C, and dried (placed in a vacuum drying oven at a temperature of 50°C) to obtain a white solid The intermediate product of trifluorooctyl p-hydroxybenzoate.
[0072] In a three-necked flask equipped with a magnetic stirrer, a thermometer, a constant pressure dropping funnel, and a reflux condenser, add 22 grams of dichloromethane, 1.24 grams of triethylamine, and 4.88 grams of tridefluorooctyl p-hydroxybenzoate in sequenc...
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