Side group-modified oxygen-free polymer anion exchange membrane and preparation method thereof
An anion-exchange membrane and polymer technology, which is applied in the field of side group-modified oxygen-free polymer anion-exchange membrane and its preparation, can solve the problem that the ion conductivity and stability of the alkaline ion-exchange membrane cannot be taken into account, and achieve solvent selection Wide range, simple and fast response operation, and performance-enhancing effect
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Embodiment 1
[0041] Synthesis of amine-containing oxygen-free polymer: under ice-water bath conditions, 2.7516g (12mmol) of m-terphenyl, 1.7652g (15.6mmol) of N-methyl-4-piperidone, 12.75mL (144mmol) of triphenyl Add fluoromethanesulfonic acid into a 50mL three-necked flask, and then add 18mL of dichloromethane to make a mixed solution. After mechanical stirring for 30min, gradually raise the temperature to room temperature, and keep it at room temperature for 30h. After the reaction, the product was completely dissolved in DMSO solution with tweezers, and then precipitated with 0.5M NaOH solution to obtain a white powdery polymer. The product was repeatedly washed and soaked with deionized water and then dried to obtain a polymer for use.
[0042] Synthesis of 1-(4-bromobutyl)-1-methyl-4-piperidinium bromide salt ionic liquid: Dissolve 5mL 1,4-dibromobutane in 20mL ethyl acetate with a 50mL one-necked flask, add 2.82g of N-methylpiperidine was reacted at 60°C for 48h to obtain a precipita...
Embodiment 2
[0048] Synthesis of amino-containing oxygen-free polymer: under ice-water bath conditions, 2.7516g (12mmol) m-terphenyl, 1.7652g (15.6mmol) of N-methyl-4-piperidone, 12.75mL (144mmol) of trifluoro Add methanesulfonic acid into a 50mL three-necked flask, and then add 18mL of dichloromethane to make a mixed solution. After mechanical stirring for 30min, the temperature is gradually raised to room temperature and kept at room temperature for 30h. After the reaction, the product was completely dissolved in DMSO solution with tweezers, and then precipitated with 0.5M NaOH solution to obtain a white powdery polymer. The product was repeatedly washed and soaked with deionized water and then dried to obtain a polymer for use.
[0049] Synthesis of 1-(6-bromohexyl)-1-methyl-4-piperidinium bromide salt ionic liquid: Dissolve 5mL 1,6-dibromohexane in 20mL ethyl acetate with a 50mL one-necked flask, add 2.82 g N-methylpiperidine, reacted at 60°C for 48h, and obtained the precipitated prod...
Embodiment 3
[0055] Synthesis of amino-containing oxygen-free polymer: same as Example 2
[0056] Synthesis of 1-bromohexyl-1-methylpyrrolidine bromide salt ionic liquid: Dissolve 5mL of 1,6-dibromohexane in 15mL of ethyl acetate in a 50mL one-necked flask, add 1.754g of N-methylpyrrolidine, After reacting at 60°C for 24h, a precipitated product in the form of milky white powder was obtained. The product was repeatedly washed with ethyl acetate for 3 to 5 times, and vacuum-dried at 60° C. for 12 hours to obtain a milky white powdery ionic liquid.
[0057] Preparation of hexane-branched pyrrolidine functionalized polymer anion-exchange membrane without ether oxygen bond: under nitrogen protection, weigh 0.5 g of amino-substituted polymer without ether oxygen bond and add it to a 50 mL three-necked flask, dissolve it with 10 mL DMSO, and wait for polymerization After the substance was fully dissolved, 0.7592g of 1-bromohexyl-1-methylpyrrolidine bromide in DMSO solution was added, and the re...
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