| Project/Area Number |
09651005
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
高分子構造・物性(含繊維)
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| Research Institution | Kansai University |
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Principal Investigator |
URAGAMI Tadashi Kansai University, Faculty of Engineering, Professor, 工学部, 教授 (80067701)
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| Co-Investigator(Kenkyū-buntansha) |
MIYATA Takashi Kansai University, Faculty of Engineering, Associate Professor, 工学部, 助教授 (50239414)
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| Project Period (FY) |
1997 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1997: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | Polymer / Membrane / Chemical Structure / Physical Structure / Benzene / Cyclohexane / Aqueous Alcohol Solution / Removal of Hydrocarbons / Permselectivity / ベンゼン / 透過分離機構 |
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| Research Abstract |
Characteristics of permeation and separation for benzene/cyclohexane mixtures in pervaporation through polymer membranes were studied from the viewpoint of chemical and physical structure of the membranes, and mechanism of permeation and separation is also discussed.
Liquid crystalline polymer membranes from poly(dimethyl siloxane)(PDMS) with mesogen group and methylmethacrylate-methacrylic acid copolymer membranes cross-linked with metal ions showed benzene-permselectivity. This permselectivity is significantly related to the chemical and physical structure of the membranes. Because depression of swelling of the membrane due to feed mixtures is remarkably improved permselectivity, chitosan and cellulose were benzoylated. These benzoylated chitosan and cellulose membranes were very high benzene-permselective. It made that hydrophilic-hydrophobic balance of the membrane was very important clear.
Effect of factor of the membrane structure on the permselectivity for aqueous alcohol solutions was investigated from the viewpoints of chemical modification of hydrophilic polymers and construction of physical structure of the membrane. Optimum in degrees of hydrophilicity and cross-link of quaternized chitosan membranes gave high water-permselective. Poly [1-(trimethylsilyl)-1-propyne] membranes surface-modified with a PDMS-g-poly(fluoroacrylate) showed high ethanol-permselectivity for aqueous ethanol solutions.
Graft copolymer membranes prepared from DMS macromonomer and alkylmethacrylates showed high volatile organic compound(VOC)-permselectivity for an aqueous dilute VOS solution. This permselectivity was significantly influenced by composition of graft copolymer, and furthermore was deeply related to morphology in microphase separated structure of the graft copolymer membranes.
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