博碩士論文 91324043 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學工程與材料工程學系zh_TW
DC.creator廖建達zh_TW
DC.creatorChien-Ta Liaoen_US
dc.date.accessioned2004-7-9T07:39:07Z
dc.date.available2004-7-9T07:39:07Z
dc.date.issued2004
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=91324043
dc.contributor.department化學工程與材料工程學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract本研究以氧化鋁為擔體,利用沈澱固著法製備成奈米氧化鋁擔體金觸媒(簡稱為Au/γ- Al2O3觸媒),同時利用感應耦合電漿原子放射光譜儀(ICP-AES)、氮吸附法、熱重分析(TGA)、X射線繞射分析儀(XRD)、掃描式電子顯微鏡(SEM)、穿透式電子顯微鏡(TEM)、X-射線光電子分析儀(XPS)等各項儀器與分析技術,分別對擔體及觸媒進行鑑定,並利用甲醇部份氧化反應為為催化活性的測試,藉以評估奈米氧化鋁擔體金觸媒應用於質子交換膜燃料電池(PEMFC)的可行性。由ICP-AES 分析結果,顯示Au/γ- Al2O3觸媒的金載量取決於pH值及製備時氯化金溶液的濃度,在低於等電位點金可達到60 %;氮吸附分析指出,以沈澱固著法製備的Au/γ- Al2O3觸媒,BET比表面積幾乎不會受煅燒溫度及載量的影響。從XRD圖譜中,可發現不同沈澱劑所形成不同大小的金晶粒。從TEM分析結果,發現Au/γ- Al2O3觸媒製備時pH值若超過等電位點時,可形成金晶粒大小約4 nm,且均勻分散在擔體表面上。而XPS分析結果可發現,以沈澱固著法所製備的Au/γ- Al2O3觸媒,表面會形成氫氧化金沈澱,且隨著煅燒溫度的增加,會逐漸熱解成金屬態的金。經過反應活性的測試,我們找出最佳的操作變數為金載量需小於1 wt%、製備pH值為9、沈澱劑為Na2CO3、煅燒溫度為573 K。若以此條件所製備出的觸媒,於523 K下進行甲醇部份氧化反應,能得到最佳的甲醇轉化率與氫氣選擇率。與文獻上銅觸媒、鈀觸媒的催化結果做比較,Au/γ- Al2O3觸媒不僅催化活性高,且幾乎沒有CO氣體的產生。由此結果可看出奈米金觸媒對於催化甲醇部份氧化反應,能夠選擇性的抑制CO的產生,相信可應用在燃料電池的氫氣源供應。zh_TW
dc.description.abstractIn this work, γ-Al2O3 was used as a catalyst support. Nanosized Au/γ-Al2O3 catalysts were prepared by the deposition-precipitation method. The supported Au catalysts were characterized by inductively coupled plasma-atomic emission spectrometer (ICP-AES), X-ray diffraction (XRD), thermogravimetric analyzer(TGA), nitrogen adsorption method , scanning electron microcopy (SEM), transmission elecron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The ICP-AES analysis indicates that gold loading is significantly affected by the preparation pH value. When the pH value is below isoelectric point of support precipitates reach 60% loading. The nitrogen adsorption analysis shows that the catalyst preparation procedure does not affect the surface area of the support. Furthermore , the TEM analysis demonstrates that the mean size of gold crystallites decreases with increasing pH value. Au/γ-Al2O3 catalysts was tested by the partial oxidation of methanol at 503-563K. The results indicate that the optimal preparations and operating conditions for best methanol conversion and hydrogen selectivity are 0.15 wt% in gold loading, 673 K in calcinations temperature, Na2CO3 in precipitation reagent, pH value 9 in prepared condition and 563K in reaction temperature. Moreover, compare to copper and palladium catalysts in POM reaction, Au/γ-Al2O3catalysts display good activity and highly CO selectivity. Nanosized Au/γ-Al2O3 catalysts may have an opportunity to apply in proton exchange membrane fuel cell.en_US
DC.subject甲醇部份氧化zh_TW
DC.subject氧化鋁zh_TW
DC.subject金觸媒zh_TW
DC.subjectpartial oxidation of methanolen_US
DC.subjecthydrogenen_US
DC.subjectaluminaen_US
DC.subjectparticle size effecten_US
DC.subjectgold catalysten_US
DC.title氧化鋁擔載奈米金觸媒之製備與應用研究zh_TW
dc.language.isozh-TWzh-TW
DC.titlePreparation and application of alumina-supported gold catalystsen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明