博碩士論文 993204034 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楊銘彥zh_TW
DC.creatorMing-Yen Yungen_US
dc.date.accessioned2012-6-22T07:39:07Z
dc.date.available2012-6-22T07:39:07Z
dc.date.issued2012
dc.identifier.urihttp://ir.lib.ncu.edu.tw:444/thesis/view_etd.asp?URN=993204034
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氧化錳-氧化鈰觸媒對揮發性有機廢氣焚化有良好活性,奈米鈀/氧化鈰觸媒對於甲苯完全氧化反應有很高的活性。因此,吾人製備鈀/氧化錳-氧化鈰觸媒以期達到更佳的反應活性。在本研究中,製備一系列不同錳/(錳+鈰)比例的鈀/氧化錳-氧化鈰觸媒。先以共沉澱法及氧化還原沉澱法製備氧化錳-氧化鈰,再以初濕含浸法製備0.5 wt. %之鈀觸媒。觸媒鑑定方面,主要是以X光繞射儀(XRD),穿透式電子顯微鏡(TEM),高解析度穿透式電子顯微鏡(HRTEM),X光電子能譜儀(XPS)與程溫還原系統(TPR),進行鑑定與分析。並使用甲苯作為本研究觸媒焚化之指標物。反應物甲苯之進料濃度為8.564 g/m3 (2085 ppm),空間流速為10,000 h-1。TEM與HRTEM圖中顯示鈀的顆粒大小約為3到5奈米,且均勻分布於擔體上,其結果與XRD結果一致。由XPS中可發現在適當的錳/(錳+鈰)比例下,有助於鈀元素態與高價錳的比例增加,同時也增進其反應活性。由氧化還原沉澱法製備之氧化錳-氧化鈰擔體較共沉澱法製備之擔體有更大的體積、孔洞體積、表面積、更高的表面錳含量及錳價態,且有特殊的棒狀型顆粒,故擁有更好的反應活性。從活性測試中,鈀/氧化錳-氧化鈰觸媒之反應活性優於鈀/氧化錳、鈀/氧化鈰混合觸媒,證明鈰與錳之間有好的交互作用。實驗結果顯示鈀/氧化錳-氧化鈰觸媒之反應活性優於單一擔體之觸媒,是因為氧化錳與鈀與氧化鈰間有協同作用使得反應活性佳。對於甲苯完全氧化反應,鈀/氧化錳-氧化鈰觸媒是非常好的。 zh_TW
dc.description.abstractMnOx-CeO2 was reported to be active for VOCs combustion and Pd/CeO2 were reported to be very active to destruct toluene from this lab. Therefore, combination of MnOx-CeO2 and palladium is a potential candidate to achieve a catalyst with high activity. In this study, a series of Pd/MnOx-CeO2 catalysts with various ratios of Mn/(Mn + Ce) were prepared. MnOx-CeO2 supports were prepared by co-precipitation method and redox-precipitation method, Pd was loaded by incipient-wetness impregnation method. The Pd loadings in all samples were fixed at 0.5 wt.%. The catalysts were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and temperature-programmed reduction (TPR). The catalysts were tested for total oxidation of toluene. The feed concentration of toluene was 8.564 g/m3 (2085 ppm), with GHSV= 10,000 h-1. The TEM and HRTEM images showed that Pd particle sizes were 3–5 nm and well-dispersed on the support. This result is consistent with the XRD studies. XPS study indicated that the suitable ratio of Mn/(Mn + Ce) able increased the proportion of metallic palladium, the content of high valance state manganese and the catalytic activity. Redox-precipitation prepared MnOx-CeO2 supports have a larger pore volume, surface area, higher manganese valance state, and higher surface manganese amount compare with MnOx-CeO2 prepared by CP method. Moreover MnOx-CeO2 prepared by RP method had a special tube-like shape, so that Pd/MnOx-CeO2 RP had a higher activity. Pd/MnOx-CeO2 catalyst was better than the physically-mixed Pd/MnOx and Pd/CeO2 catalyst, which indicates that there is a strong interaction between ceria and manganese. In conclusion, Pd/MnOx-CeO2 catalysts were superior to Pd/MnOx and Pd/CeO2 catalysts due to the synergetic effect between Ce and Mn. Pd/MnOx-CeO2 catalysts are very promising for toluene destruction. en_US
DC.subject甲苯zh_TW
DC.subject氧化錳-氧化鈰zh_TW
DC.subject氧化鈰zh_TW
DC.subject氧化錳zh_TW
DC.subjectzh_TW
DC.subject觸媒焚化zh_TW
DC.subjectCeO2en_US
DC.subjectMnOxen_US
DC.subjectMnOx-CeO2en_US
DC.subjecttolueneen_US
DC.subjectPalladiumen_US
DC.subjectCatalytic combustionen_US
DC.title奈米鈀觸媒擔載於氧化錳-氧化鈰於甲苯完全氧化反應之應用zh_TW
dc.language.isozh-TWzh-TW
DC.titleThe Catalytic Properties of Pd/MnOx-CeO2 on Destruction of Tolueneen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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