Method for preparing good-stability super-hydrophobic fabrics
A super-hydrophobic and stable technology, applied in physical treatment, textiles and papermaking, fiber treatment, etc., can solve the problems of limiting the practical application of super-hydrophobic fabrics, poor stability of super-hydrophobic surfaces, and insufficient bonding of compounds and fabric fibers. , to achieve the effect of being convenient for mass production, maintaining mechanical properties and gloss, and low cost
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Embodiment 1
[0036] Measure 96 μL of tetraethoxysilane and 392 μL of methyltriethoxysilane into a round-bottomed flask filled with 20 mL of saturated ethanol-ammonia solution, and stir magnetically for 10 minutes to obtain a uniform alcohol-ammonia solution of organosilane; add 1.5 mL of water, heated up to 50°C within 0.5h, and kept at this temperature for 48h; cooled to room temperature, and obtained the crude product by suction filtration; washed with 10mL of methanol and filtered three times, then vacuum dried at 50°C for 3h to obtain organosilane polymerization things. Weigh 60mg organosilane polymer, dissolve in 10mL toluene, stir magnetically for 5min, disperse ultrasonically for 5min, and then put 2×2cm 2 The polyester fabric was immersed in it, and after standing for 5 minutes, it was ultrasonically treated for 20 minutes. The fabrics were taken out to dry and evaluated for performance.
[0037] The evaluation results of the sample superhydrophobicity and stability are shown in ...
Embodiment 2
[0039]Measure 538 μL of tetraethoxysilane, 122 μL of aminopropyltrimethoxysilane and 264 μL of octyltriethoxysilane into a round bottom flask filled with 40 mL of saturated ethanol-ammonia solution, and stir magnetically for 10 minutes to obtain a uniform organic Alcohol-ammonia solution of silane; add 6.5mL of water, raise the temperature to 50°C within 0.5h, and keep the temperature for 24h; cool to room temperature, and obtain the crude product by suction filtration; °C for 3 hours in vacuum to obtain an organosilane polymer. Weigh 40 mg of the polymer, dissolve it in 5 mL of toluene, stir it magnetically for 5 min, and disperse it ultrasonically for 5 min, then place 2×2 cm 2 The cotton fabric was immersed in it, and after standing for 5 minutes, it was ultrasonically treated for 30 minutes. The fabrics were taken out to dry and evaluated for performance.
[0040] The evaluation results are shown in Table 1. For photos of samples see figure 2 , the photo after 200 fri...
Embodiment 3
[0042] Measure 282 μL of tetraethoxysilane, 118 μL of 3-(2,3-glycidoxy)propyltrimethoxysilane and 418 μL of hexadecyltriethoxysilane, and add them to 20 mL of saturated ethanol-ammonia In a round-bottomed flask of the solution, stir magnetically for 10 minutes to obtain a homogeneous alcohol-ammonia solution of organosilane; add 2.8mL of water, raise the temperature to 40°C within 0.5h, and keep the temperature for 48h; cool to room temperature, and obtain crude The product was washed with 10 mL of methanol-suction filtered three times, then dried in vacuum at 50° C. for 3 h to obtain an organosilane polymer. Weigh 40 mg of the polymer, dissolve it in 5 mL of toluene, stir it magnetically for 5 min, disperse it ultrasonically for 5 min, and then spray the solution onto 2×2 cm 2 on silk fabric. After ultrasonic treatment for 10 min, the fabric was treated at 80 °C for 1 h, and its performance was evaluated.
[0043] The evaluation results are shown in Table 1. For photos of ...
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