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dc.contributorChun-Hsiung Hungen_US
dc.contributor.authorLu, Yu-Wenen_US
dc.identifier.citation中文參考文獻 圖書 方良吉、王漢英、曲新生、朱時梁、朱義仁、江秋桂、李宏台、李清庭、李勝隆、辛華煜、何無忌、何建輝、林法正、林秋裕、林炳明、林振源、林國安、吳英秦、吳建勳、吳煌、邱錦松、胡耀祖、徐恆文、桂人傑、曹芳海、黃正忠、黃明熙、黃秉鈞、陳清山、陳錫銓、陳輝俊、張翼、楊秉純、楊建裕、詹益亮、蔡松雨、鄭名山、賴炎生、劉志放、盧俊鼎、顏文治、顏志偉、蕭弘清、藍崇文與羅仕明 (2010) 2010年能源產業技術白皮書。經濟部能源局。 期刊論文 林秋裕與張逢源 (2008) 生物氫能面面觀。物理雙月刊 3:389-394。 張逢源與林秋裕 (2008) 淺談台灣生質能發展。能源報導 12:5-7。 張維欽、莊順興、羅時斌與陳建衡 (2008) 生物處理系統之溶解性微生物產物探討。工業污染防治 105:39-56。 張嘉修 (2009) 生質氫能。科學發展 433:32-35。 張福傳、張美琴與蘇郁雅 (2011) 台灣有機廢棄物厭氧醱酵產製生質能之期待與展望。化工技術 19:124-137。 吳珮瑛、林宗昱與劉哲良 (2010) 由 APEC 區域組織邁入國際社會參與碳排放交易之結果——對台灣的啟示。台灣國際研究季刊 6:143-184。 黃啟裕 (2008) 纖維素產氫技術在生質能源之發展。農業生技產業季刊 13:54-60。 張佩雯 (2011) 探討微生物電解電池於不同操作條件下之產氫效能與菌群結構。碩士論文。國立中興大學,台中。 英文參考文獻 Books Logan, B.E. (1999) Environmental transport processes. Wiley. Logan, B.E. (2008) Microbial fuel cells. John Wiley & Sons. Hallenbeck, P.C. (2012) Microbial Production of Fatty-Acid-Based Biofuels. Microbial Technologies in Advanced Biofuels Production, in: Hallenbeck, P.C. (Ed.). Springer US, pp. 213-230. 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dc.description.abstract近年來生質氫能逐漸備受重視,原因為氫氣除了具有可儲存、運輸等優點外,其燃燒後產生之熱值約為汽油的三倍,且燃燒產物只有水與熱,為一潔淨無污染之能源載體。微生物電解電池(Microbial electrolysis cells, MECs)為一新穎產氫技術,藉由輸入外部能量的方式,可克服熱力學屏障,將厭氧暗醱酵程序所生成之液態代謝物藉由微生物催化電解的方式轉換成氫氣,進而提升整體氫氣產量。由於暗醱酵程序之液態代謝物多為丁酸、乙酸等有機物質,因此本研究以丁酸作為基質,探討其應用於微生物電解電池上之可行性與效能表現程度。 實驗以綠川底泥作為植種來源並以連續批次操作方式進行。研究結果顯示丁酸可於每批次結束後完全降解,僅少量乳酸累積,sCOD去除率平均可達95 %;庫侖氫氣回收率(rCE)平均約為15 %;菌相分析結果顯示系統中存在丁酸氧化菌Syntrophomonas sp.及胞外產電菌Geobacter metallireducens;在氣相組成方面,陽極槽氣體多為甲烷與二氧化碳,陰極槽則為甲烷與氫氣。藉由甲烷菌功能性基因分析確認系統中存在嗜氫甲烷菌,故實驗後期以縮短批次循環時間作為甲烷控制策略,結果顯示此操作策略確實可提升陰極槽氫氣產量,但對減少甲烷氣體無顯著影響。 由於植種來源內存在對MEC產氫表現有負面影響的甲烷菌群,故後續實驗中以BES(2-溴乙烷磺酸鈉)作為甲烷抑制劑,探討不同添加策略對MEC系統效能及微生物族群結構變化之影響。實驗結果顯示MEC在陰極槽添加BES 0.5 mM時可維持較佳效能,此操作時期的液相組成、COD去除率等皆可達到一定處理效果;菌相分析結果則顯示BES-added MEC陽極槽主要微生物為Pseudomonas sp.,系統中缺少可利用丁酸的Geobacter metallireducens與Syntrophomonas sp.可能是造成丁酸降解效率不佳的原因之一;陰極槽中所發現的Serratia marcescens、Stappia sp.、Neisseria animaloris等微生物可能會有與質子競爭電子之現象發生;兩電極上生物膜則皆存在可分泌EPS的Serratia marcescens。有文獻指出與BES長時間接觸下可能會改變包含產電菌在內的菌群結構,故推測添加50 mM BES於陽極槽中會對微生物族群的正常代謝作用造成間接影響,可能因此造成MEC中丁酸降解效果不佳。zh_TW
dc.description.abstractHydrogen productions via biological methods draw a lot of attentions in recent years. Hydrogen is one of the clean energy carriers due to its advantages on storage, transport and high heating value (three times of what gasoline has). Furthermore, it produces only water and heat after combustion. Microbial electrolysis cells (MECs), a novel hydrogen production technology, use microbial catalyzing electrolysis form to convert soluble organic metabolites into hydrogen by inputting external voltage to overcome the thermodynamics barrier. As butyrate and acetate are the main soluble metabolites of dark fermentation process, this study use butyrate as substrate to investigate the possibility for using effluent from anaerobic dark fermentation processes on MECs. In this study, sediment collected from Luchuan River was selected as the MEC inoculums and the reactor was operated in sequencing batch mode. Results showed that butyrate was utilized completely after each batch with small amounts of lactate remained. Average sCOD removal rate was around 95%, and the average Coulombic hydrogen recovery was about 15%. Microbial communities analysis showed the dominant bacteria were butyrate-utilizing bacteria Syntrophomonas sp. and exoelectrogens Geobacter metallireducens. For gas composition, CH4 and CO2 were the main gases in anode chamber and CH4 and H2 were detected in the headspace of cathode chamber. Since hydrogenotrophic methanogen was found to exist in the MEC using methanogenic functional gene analyzing technique, operation time for each batch cycle was shorten as the strategy of methane control. Results showed that this strategy could promote hydrogen production, but had no significant benefit on inhibiting methane production. Furthermore, Sodium 2-bromoethanesulfonate (BES) was selected as the methanogen-specific inhibitor to investigate the effects of MEC system efficiency and microbial community structure under different BES-added strategies. Better efficiencies were observed when adding 0.5 mM BES in the cathode chamber as showing in the liquid composition and COD removal rate. Microbial community results revealed that Geobacter metallireducens and Syntrophomonas sp. did not exist in the MES system after BES addition. This might be one of the reasons for the lower butyrate-degrading efficiency. Serratia marcescens, Stappia sp. and Neisseria animaloris which might compete for protons existed in the cathode. Moreover, Serratia marcescens which could secrete extracellular polymeric substances (EPS) was found on the anode and cathode biofilms. Since long-term exposure to BES might alter the anode microbial community including methanogens and exoelectrogens was reported in the reference, we speculate that adding 50 mM BES to the anode chamber could indirectly affect the metabolisms of microorganisms, and thus decreased the butyrate-degrading efficiency.en_US
dc.description.tableofcontents中文摘要 i 目錄 iv 圖目錄 vi 表目錄 viii 第一章 前言 1 第一節 研究緣起 1 第二節 研究目的 2 第二章 文獻回顧 3 第一節 氫能源概述 3 一、能源發展 3 二、再生能源 5 三、氫能源 7 第二節 生物電化學系統概述 15 一、微生物燃料電池(Microbial fuel cells, MFCs) 16 二、微生物電解電池(Microbial electrolysis cells, MECs) 18 第三節 微生物電解電池之作用機制 20 第四節 微生物電解電池效能之影響因素─微生物 26 一、電化學活性微生物 26 二、抑制系統效能之微生物 33 第五節 微生物電解電池表現效能之評估參數 37 一、電流密度(Current density, CD) 37 二、氫氣產率(Hydrogen yield) 38 三、氫氣回收率(Hydrogen recovery) 39 四、氫氣體積產率(Volumetric hydrogen production rate, Qmax) 41 五、氫氣損失(Hydrogen losses) 41 六、能量回收(Energy recovery) 43 第六節 文獻閱讀心得與研究方向擬定 48 第三章 實驗材料與方法 49 第一節 實驗架構 49 第二節 實驗設備 51 第三節 實驗方法 52 一、微生物植種來源 52 二、藥品試劑─培養基、緩衝溶液與甲烷抑制劑 52 三、微生物電解電池之連續批次實驗 54 第四節 分析儀器與方法 55 一、分子生物技術分析 55 二、水質項目分析 59 三、氣相組成分析 59 四、液相組成分析 60 第五節 實驗內容 61 第四章 結果與討論 63 第一節 以丁酸為基質之微生物電解電池試驗 63 一、MEC連續批次操作實驗 63 二、MEC系統效能探討 65 三、MEC系統之微生物族群結構分析 76 四、初步結論 87 第二節 MEC系統之甲烷抑制操作策略探討 88 一、有無添加甲烷抑制劑之連續批次實驗 89 二、甲烷抑制操作實驗組MEC之系統效能探討 91 三、甲烷抑制操作實驗組MEC之微生物族群結構分析 103 四、初步結論 117 第三節 綜合討論 119 第五章 結論與建議 123 第一節 結論 123 第二節 建議 126 參考文獻 127zh_TW
dc.subjectMicrobial electrolysis cellsen_US
dc.subjectMethane inhibitionen_US
dc.titleSystem efficiency and microbial community analysis of microbial electrolysis cells using butyrate as the substrateen_US
dc.typeThesis and Dissertationzh_TW
item.openairetypeThesis and Dissertation-
item.fulltextno fulltext-
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