Chitosan modified diatom-based As (V) ion imprinting material and preparation and application methods thereof
A technology of ion imprinting and chitosan, applied in chemical instruments and methods, other chemical processes, water/sludge/sewage treatment, etc., can solve problems such as poor selective adsorption effect
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[0050] The present invention provides a kind of preparation method based on chitosan modified diatom As(V) ion imprinting material, comprising the following steps:
[0051] After mixing diatomite and methanesulfonic acid solution, activate it to obtain activated diatomite;
[0052] Chitosan, As(V) solution and HAc solution are mixed to obtain chitosan sol;
[0053] Mixing the activated diatomite, chitosan sol and γ-glycidyl etheroxypropyltrimethoxysilane for polymerization reaction to obtain a diatom-based cross-linked polymer;
[0054] The template ions in the diatom-based cross-linked polymer are eluted with hydrochloric acid solution to obtain an ion imprinted material based on chitosan-modified diatom As(V).
[0055] The invention mixes the diatomite (Dt) and methanesulfonic acid solution to activate to obtain the activated diatomite (At-Dt). In the present invention, the dosage ratio of diatomaceous earth and methanesulfonic acid solution is preferably 30g:100mL, and th...
Embodiment 1
[0082] (1) Preparation of activated diatomite (At-Dt)
[0083] Weigh 30g of diatomaceous earth (Dt) into a 500mL flask, add 100mL of 33% methanesulfonic acid solution, and heat to reflux at 50°C for 8h. After cooling, filter with suction, wash with ultrapure water until neutral, and dry the solid at 80°C to obtain activated diatomite.
[0084] (2) Preparation of IIP
[0085] 1.5g of chitosan (CS) was dispersed in 5mL of 2g / L As(V) solution (pH=5), and then 20mL of 2% HAc solution was added until the chitosan was dissolved, and then 5g of activated diatomaceous earth was added for 25 Stir magnetically at ℃ for 2 hours, add 5mL DGTMS, and stir until gelatinous under the same conditions; dry at 50℃, grind through a 100-mesh sieve, add 100mL of 0.5mol / L hydrochloric acid, stir at 25℃ for 2h, and filter with suction; Wash with ultrapure water until the supernatant is neutral and free of As, filter with suction, and dry at 50°C to obtain IIP.
[0086] (3) Preparation of NIP
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