Core-shell type fluorine-free waterproof finishing agent, and preparation method and application thereof
A fluorine-free waterproof, core-shell type technology, applied in fiber treatment, textiles and papermaking, liquid-repellent fibers, etc., can solve problems such as refractory and unsafe, and achieve good dynamic water repellency and excellent surface Performance, long-lasting and stable surface energy effect
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Embodiment 1
[0087] Synthesis of Large Size Particles (I):
[0088] 1) Mix 125.0g absolute ethanol and 50.0g ammonia water at room temperature;
[0089] 2) Add 50.0 g of silicon dioxide, titanium dioxide or zinc oxide particles with a particle diameter of 50-500 nm to the mixed solution in 1), and ultrasonicate for 30 minutes.
[0090] 3) Add 0.5 g of vinyltrimethoxysilane and / or γ-methacryloxypropyltrimethoxysilane to the mixture of 2), and ultrasonicate for 120 minutes;
[0091] 4) The suspension obtained in 3) was filtered with a Buchner funnel, the filter cake was washed three times with deionized water and absolute ethanol and then filtered, and the obtained filter cake was dried at 120° C. to obtain large-diameter particles (I).
Embodiment 2
[0093] Synthesis of large particle size particle dispersion (II):
[0094] 100ml H 2 O. Mix 0.3g emulsifier 1-allyloxy-3-(4-nonylphenol)-2-propanol polyoxyethylene (10) ether ammonium sulfate (DNS-86) and 0.10g NaOH into 100ml three Neck round bottom flask was stirred for 30min, then slowly added 15g KH-570 (3-(methacryloyloxy)propyltrimethoxysilane), and continued the reaction at room temperature for 24 hours, adjusted the temperature to 50°C and continued Stirring was carried out for 1 day to obtain a large-diameter particle dispersion (II).
Embodiment 3
[0096] Synthesis of Reactive Inorganic Silicon Monomer (I):
[0097] 1) Mix 125.0g absolute ethanol and 50.0g ammonia water at room temperature;
[0098] 2) Add 50.0 g of silicon dioxide nanoparticles with a particle size of 20 nm to the mixed solution of 1), and sonicate for 30 minutes;
[0099] 3) Add 0.1g of vinyltrimethoxysilane and 2.5g of dodecyltrimethoxysilane to the mixture of 2), and ultrasonicate for 120 minutes;
[0100] 4) Filter the suspension obtained in 3) with a Buchner funnel, wash the filter cake three times with deionized water and absolute ethanol and then filter, and dry the obtained filter cake at 120°C to obtain the reactive inorganic silicon monomer (I) .
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