Cellulose acetate-based ultrafiltration membrane for separating anionic dye from heavy metal and preparation method of cellulose acetate-based ultrafiltration membrane
A cellulose acetate, anionic dye technology, applied in chemical instruments and methods, ultrafiltration, semi-permeable membrane separation, etc., can solve the problems of pollution, reduction, inability to clean for a long time, etc., to improve the retention rate, high efficiency, Good market application prospects and the effect of industrialized production value
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Embodiment 1
[0034] Take 10.00g of HNTs and add 40.00g of HNTs with a mass fraction of 10% hydrochloric acid, stir magnetically for 6 hours at 25°C, wash the acid-washed HNTs with a large amount of deionized water, and centrifuge until the supernatant is neutral, then Place the washed HNTs in a vacuum drying oven at 110°C for 24 hours to obtain dried HNTs; weigh 3.0 g of dried HNTs and add 6.0 ml of N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane and 100ml of toluene mixed solution, refluxed at 110°C for 24h, after the reaction, the modified HNTs was washed with a large amount of deionized water and ethanol by centrifugation repeatedly to wash off the unreacted N-β-(aminoethyl)- γ-Aminopropyltrimethoxysilane, after washing with water, place the solid in a vacuum oven at 80°C for 12 hours to obtain N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane modified HNTs, denoted as KHNTs.
[0035] Weigh 0.04g of the obtained KHNTs and dissolve in 16.0g of dimethylacetamide, ultrasonically treat for 30m...
Embodiment 2
[0039] Take 10.00g of HNTs and add 40.00g of HNTs with a mass fraction of 10% hydrochloric acid, stir magnetically for 6 hours at 25°C, wash the acid-washed HNTs with a large amount of deionized water, and centrifuge until the supernatant is neutral, then Place the washed HNTs in a vacuum drying oven at 110°C for 24 hours to obtain dried HNTs; weigh 3.00 g of dried HNTs and add 6.00 ml of N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane and 100ml of toluene mixed solution, refluxed at 110°C for 24h, after the reaction, the modified HNTs was washed with a large amount of deionized water and ethanol by centrifugation repeatedly to wash off the unreacted N-β-(aminoethyl)- γ-Aminopropyltrimethoxysilane, after washing with water, place the solid in a vacuum oven at 80°C for 12 hours to obtain N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane modified HNTs, denoted as KHNTs.
[0040] Weigh 0.08g of the obtained KHNTs and dissolve in 16.00g of dimethylacetamide, ultrasonically treat for ...
Embodiment 3
[0044] Take 10.00g of HNTs and add 40.00g of HNTs with a mass fraction of 10% hydrochloric acid, stir magnetically for 6 hours at 25°C, wash the acid-washed HNTs with a large amount of deionized water, and centrifuge until the supernatant is neutral, then Place the washed HNTs in a vacuum drying oven at 110°C for 24 hours to obtain dried HNTs; weigh 3.00 g of dried HNTs and add 6.00 ml of N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane and 100ml of toluene mixed solution, refluxed at 110°C for 24h, after the reaction, the modified HNTs was washed with a large amount of deionized water and ethanol by centrifugation repeatedly to wash off the unreacted N-β-(aminoethyl)- γ-Aminopropyltrimethoxysilane, after washing with water, place the solid in a vacuum oven at 80°C for 12 hours to obtain N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane modified HNTs, denoted as KHNTs.
[0045] Weigh 0.12g of the prepared KHNTs and dissolve in 16.00g of dimethylacetamide, ultrasonically treat for ...
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