博碩士論文 992203047 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator王偉豪zh_TW
DC.creatorWei-Hau Wangen_US
dc.date.accessioned2012-7-24T07:39:07Z
dc.date.available2012-7-24T07:39:07Z
dc.date.issued2012
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=992203047
dc.contributor.department化學學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract本研究引入團聯共聚物 (block copolymer) 的概念,將高分子以原子轉移自由基聚合反應 (ATRP, Atom Transfer Radical Polymerization) 分兩階段聚合:第一段是聚合 styrene而得到poly(styrene)-Br,第二段則是聚合帶有咪唑鹽 (imidazolium group) 的 [VBMI][BF4] (1-(4-vinylbenzyl)-3-methyl-imidazolium tetrafluoroborate) 而得到團聯共聚物 poly(styrene-b-[VBMI][BF4])。藉由調控第二段 [VBMI][BF4] 的聚合時間而得到不同長度的親水端。此系列高分子薄膜在常溫去離子水中導電度最高有 0.074 S/cm,在 1M KOH 水溶液中導電度最高則有 0.107 S/cm 的表現,有望可應用在固態鹼性燃料電池當中。 zh_TW
dc.description.abstractThe hydroxide-conducting block copolymer membranes were synthesized by two steps. Firstly, atom transfer radical polymerization (ATRP) of styrene gave poly(styrene)-Br as a macroinitiator. Secondly, poly(styrene-b-[VBMI][BF4]) were synthesized by ATRP using the above macroinitiator with [VBMI][BF4], 1-(4-vinylbenzyl)-3-methyl- imidazolium tetrafluoroborate. Via controling the reaction time and temperature of the second ATRP, different ratio (hydrophobic block and hydrophilic block) of block copolymers were synthesized. At room temperature, the highest conductivity of the membranes can reach up to 0.074 S/cm (under DI H2O) and 0.107 S/cm (under 1M KOH solution). The results exhibit these block ionomeric membranes are potential new type anion exchange membranes in SAFCs (solid alkline fuel cells). en_US
DC.subject陰離子傳導膜zh_TW
DC.subject咪唑鹽zh_TW
DC.subject團聯高分子zh_TW
DC.subjectBlock Copolymeren_US
DC.subjectImidazolium-Functionalizeden_US
DC.subjectAnion Exchange Membraneen_US
DC.title具咪唑鹽團聯高分子之陰離子傳導膜的開發與製備zh_TW
dc.language.isozh-TWzh-TW
DC.titleSynthesis and Characterization of Novel Anion Exchange Membrane Based on Imidazolium-Functionalized Block Copolymer for Solid Alkaline Fuel Cellsen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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