Preparation method of cellulose-based interpenetrating network polymer hydrogel
An interpenetrating network, cellulose-based technology, applied in the field of cellulose-based interpenetrating network polymer hydrogels, to achieve the effects of improving specific capacitance, high porosity, and improving flexibility
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Embodiment 1
[0029] This embodiment provides a preparation method of polyacrylic acid / cellulose grafted (N-(4-aminophenyl)acrylamide) grafted polyaniline interpenetrating network polymer hydrogel, which specifically includes the following steps:
[0030] 1) Synthesis of N-(4-aminophenyl)acrylamide
[0031] Add 2.5g of p-phenylenediamine and 0.5g of triethylamine into a three-necked flask containing 100g of dichloromethane, and dissolve them with magnetic stirring at room temperature under the condition of nitrogen protection. Add 0.7g of acryloyl chloride dropwise into the three-necked flask, and react at 1°C for 2h After the reaction, the precipitate was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure to obtain N-(4-aminophenyl)acrylamide.
[0032] 2) Preparation of cellulose porous nanofibers
[0033] Add 2g of tetrahydrofuran and 8g of N,N'-dimethylformamide into the serum bottle, then add 0.3g of cellulose acetate and 0.02g of nano-sil...
Embodiment 2
[0043] This embodiment provides a preparation method of polyacrylic acid / cellulose grafted (N-(4-aminophenyl)acrylamide) grafted polyaniline interpenetrating network polymer hydrogel, which specifically includes the following steps:
[0044] 1) Synthesis of N-(4-aminophenyl)acrylamide
[0045] Add 2.8g of p-phenylenediamine and 0.6g of triethylamine into a three-necked flask containing 100g of dichloromethane, and dissolve under nitrogen protection with magnetic stirring at room temperature. Add 0.6g of acryloyl chloride dropwise into the three-necked flask, and react at 2°C for 2h After the reaction, the precipitate was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure to obtain N-(4-aminophenyl)acrylamide.
[0046] 2) Preparation of cellulose porous nanofibers
[0047] Add 3g of tetrahydrofuran and 7g of N,N'-dimethylformamide into the serum bottle, then add 0.4g of cellulose acetate and 0.03g of nano-silicon dioxide, and stir...
Embodiment 3
[0057] This embodiment provides a preparation method of polyacrylic acid / cellulose grafted (N-(4-aminophenyl)acrylamide) grafted polyaniline interpenetrating network polymer hydrogel, which specifically includes the following steps:
[0058] 1) Synthesis of N-(4-aminophenyl)acrylamide
[0059] Add 2.2g of p-phenylenediamine and 0.4g of triethylamine into a three-necked flask containing 100g of dichloromethane, and dissolve under nitrogen protection with magnetic stirring at room temperature. Add 0.5g of acryloyl chloride dropwise into the three-necked flask, and react at 0°C for 2h After the reaction, the precipitate was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure to obtain N-(4-aminophenyl)acrylamide.
[0060] 2) Preparation of cellulose porous nanofibers
[0061] Add 4g of tetrahydrofuran and 6g of N,N'-dimethylformamide into the serum bottle, then add 0.35g of cellulose acetate and 0.025g of nano-silicon dioxide, and st...
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Abstract
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