Ionic liquid-modified mesoporous material and preparation method
A technology of ionic liquids and mesoporous materials, applied in the field of nanomaterials, can solve the problems of unreported synthesis, and achieve the effect of simple synthesis method and regular structure
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Embodiment 1
[0020] Embodiment 1 organosilane A preparation
[0021] Take 4.19g of 3-chloropropyltrimethoxysilane and 10.36g of organosilane precursor 1,2-diimidazolane dissolved in 50mL of anhydrous toluene. After 4-5 times of nitrogen replacement, under the protection of nitrogen, react in the dark at 110oC for 36 hours to obtain a milky yellow oily product. The product is washed with toluene 5-6 times, and the residual toluene is removed by rotary evaporation. Finally, the bridge-shaped bis-imidazole ionic liquid organic silane.
Embodiment 2
[0022] The preparation of embodiment 2 organosilane B-D
[0023] The preparation method of organosilane B—D is the same as that of A in Example 1, except that the precursors of B—D organosilane are 1,3-diimidazolane, 1,4-diimidazolidine, 1, 5-diimidazole pentane.
Embodiment 3
[0024] Example 3 Preparation of Ionic Liquid Modified Mesoporous Material AP
[0025] Dissolve 4.16g of P123, 22g of KCl in 100mL of 2M dilute hydrochloric acid and 30g of water, and stir at 40°C for 2h until the solution is uniform and stable to form solution 1. Dissolve 1.15g of organosilane A and 7.5g of 3-chloropropyltrimethoxysilane in 1ml methanol, and quickly added to solution 1, aged at 40°C for 24h, then transferred to a stuffy tank, crystallized at 100°C for 72h, and the white solid obtained was repeatedly washed with ethanol and centrifuged to obtain a crude product. The crude product was Soxhlet extracted with ethanol for 48 hours, and the obtained solid was dried to obtain the organically modified mesoporous material AP.
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