POSS/PNIPAM nanocomposite with reversible sol-gel transition as well as preparation method and application thereof
A nano-composite material and gel technology, which is applied in non-active ingredients medical preparations, pharmaceutical formulations, medical science and other directions, can solve the problems of limited application and low mechanical strength of PNIPAM gel, and achieves improved mechanical properties and preparation methods. and the effect of simple craftsmanship
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Embodiment 1
[0024] Synthesis of OCAPS: Add 150 mL of 3-aminopropyltriethoxysilane (silane coupling agent KH550) into 1000 mL of anhydrous methanol under magnetic stirring conditions, and after mixing well, slowly add 135 mL of concentrated hydrochloric acid to the mixture , the acid hydrolysis reaction was continued at room temperature for about two weeks, and after the reaction was completed, a white solid product was obtained by suction filtration. After vacuum drying at 40°C for 24 hours, the product OCAPS was obtained with a yield of 15%.
Embodiment 2
[0026] Preparation of 1% OCAPS / PNIPAM (the molar ratio of the two is 1%) nanocomposite: Weigh 0.05g (4.28×10 -5 mol) OCAPS and 0.4822g (4.26×10 -3 mol) NIPAM was dissolved in a container of 4mL (0.22mol) deionized water, and after complete dissolution, 0.0106g initiator potassium peroxodisulfate (KPS) and 0.0021g catalyst N,N,N',N'-tetramethylethane were added Diamine (TEMED), through nitrogen deoxygenation, put it into 37 o C reacted in a constant temperature water bath for 24 hours, then took out the material and put it in 37 o Soak C in deionized water for 5 minutes to remove unreacted monomers, initiators and catalysts to obtain the product.
Embodiment 3
[0028] Preparation of 3% OCAPS / PNIPAM (the molar ratio of the two is 3%) nanocomposite: Weigh 0.15g (1.28×10 -4 mol) OCAPS and 0.4822g NIPAM (4.26×10 -3 mol) dissolved in 4mL (0.22mol) of deionized water container, after complete dissolution, add 0.0095g initiator potassium peroxodisulfate (KPS) and 0.0019g catalyst N,N,N',N'-tetramethylethylenedi Amine (TEMED), through nitrogen deoxygenation, put the reaction vessel into 37 o C reacted in a constant temperature water bath for 24 hours, then took out the material and put it in 37 o Soak C in deionized water for 5 minutes to remove unreacted monomers, initiators and catalysts to obtain the product.
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