Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Product | HCID 22714748 | HCID 22714748 | — |
Reaction Steps
10 mass % of chloromethyl styrene and 20 mass % of triethyl amine. were reacted in acetone solvent at 40° C. for 40 hours to obtain N,N,N-triethyl(vinylphenyl)methyl ammonium chloride. This was cooled to −5° C., recrystallized and isolated, followed by dissolving the same in toluene at a concentration of 10 mass %, and 0.005 mass % of 2,2-azobis(2-methyl butyronitrile) was further dissolved therein. After nitrogen bubbling, this solution was subjected to polymerization at 50° C. for 72 hours. The solution after polymerization was reprecipitated by pouring the same in excessive amounts of methanol followed by drying to obtain a solid matter. This solid matter was dissolved in tetrahydrofuran at a concentration of 40 mass %, and the solvent was dried after impregnation of porous membrane (polyethylene-based, having weight average molecular weight of 250,000, membrane thickness of 25 μm, average pore diameter of 0.03 μm and porosity of 37%). This operation was repeated several times to produce an anion-exchange membrane 5 including a quaternary ammonium group having a halogeno ion as its counterion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399154B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1ec26f840a064d2c8984cf584cba6f4a |
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| Source note | uspto-grants-2013_03 |
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