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    题名: CuO/CeO2/MnOx/Al2O3觸媒於富氫環境下對CO選擇性氧化反應研究;Selective oxidation of CO in excess hydrogen over CuO/CeO2/MnOx/Al2O3 catalysts
    作者: 賴星魁;Shin-Quei Lai
    贡献者: 化學工程與材料工程研究所
    关键词: 一氧化碳選擇性氧化;氧化錳;銅鈰觸媒;MnOx;CeO2.PROX;CuO
    日期: 2009-06-15
    上传时间: 2009-09-21 12:31:33 (UTC+8)
    出版者: 國立中央大學圖書館
    摘要: 本研究以共沉澱法製得Ce1-xMnxO2擔體,再以含浸法製備10% CuO/Ce1-xMnxO2觸媒,藉以了解Mnn+引入CeO2對PROX反應的影響。另採工業觸媒常用的共沉澱法製備CuO/CeO2/MnOx/Al2O3觸媒,探討各成分比例對PROX反應的影響與作用。PROX反應於進料氣體比CO/O/H2/He = 1/1/50/48及質流比F/W = 10,000 mlh-1gcat-1下進行,並採用BET、TPR、Raman、XPS、Auger與脈衝式CO吸附等分析方法探討觸媒之物理特性與表面性質。 10% CuO/Ce1-xMnxO2觸媒中,Mnn+引入可進入CeO2晶格中形成Ce-Mn-O固溶物,增加擔體redox特性,引入量可達到x = 0.3而不使觸媒活性降低。共沉澱法可製得高CuO負載量且分散良好的CuO/CeO2/ MnOx/Al2O3觸媒,最適的煅燒溫度為650°C 。CuO/CeO2觸媒之CuO負載量可高達30%,而不影響T100 (90~95°C)。MnOx引入CuO/CeO2中,亦可形成固溶物,MnOx的引入不僅可協助CeO2的redox特性,MnOx本身亦扮演與CuO交互作用的協同角色,引入量可高達30%,而T100略升為95~100°C。Al2O3的引入雖可增強觸媒物理性質,但引入量不宜超過10%。CuO/CeO2/MnOx/Al2O3觸媒活性取決於CuO與CeO2是否良好接觸,各成分的引入量過多會發生聚集分離,降低CuO與CeO2接觸機會,而不利於反應,最理想的組成比例為30/40/20/10。CuO/CeO2/MnOx/Al2O3 (30/40/20/10)觸媒具有媲美CuO/CeO2與CuO/Ce1-xMnxO2觸媒的活性與選擇性,且可處理高容量的反應氣體,進料中引入CO2 與H2O雖會使觸媒活性與選擇率下降,但觸媒仍具有相當良好的穩定性,是具實用性的理想PROX反應之觸媒。 In order to realize the effect of PROX reaction when Mnn+ was incorporated into CeO2, Ce1-xMnxO2 mixed oxides were prepared as supports of 10% CuO/Ce1-xMnxO2 catalysts which prepared by impregnation method. Then CuO/CeO2/MnOx/Al2O3 catalysts were prepared by co-precipitation method for use in the PROX reaction. The effects of CuO/CeO2, MnOx/CeO2, and MnOx/Al2O3 on the selective oxidation of CO were examined and the roles of CeO2, MnOx and Al2O3 were discussed. The feed H2/CO/O2/He (50/1/1/48) were diverted to the reactor at the flow rate of 30 ml/min (F/W = 10,000 mlh-1gcat-1). The physical and surface properties of catalysts were determined by BET, XRD, TPR, XPS and pulsing adsorption of CO. For Ce1-xMnxO2, Mnn+ incorporated into the CeO2 lattice to form Ce-Mn-O solid solution and enhanced redox properties of supports for CuO/Ce1-xMnxO2 catalysts. The incorporated amount of Mnn+ could be achieved x = 0.3 without weakened activity. It could obtain high CuO loading and fine dispersion CuO/CeO2/MnOx/Al2O3 catalysts by co-precipitation method when the optimum calcinations temperature was 650°C. CuO loading amount could be as high as 30%, and the temperature (T100) for complete conversion was about 90~95oC. Introducing MnOx into CuO/CeO2 could also form Ce-Mn-O solid solution. MnOx would not only increase the mobility of lattice oxygen but also played a synergistic role interacting with CuO. Therefore, The selective oxidation of CO was not weakened as part of CeO2 replaced by MnOx less than 30%, while slightly increased T100 for 95~100°C. Incorporating Al2O3 weakened the activity. Nevertheless, an appropriate amount of Al2O3 (10%) was needed for the physical properties of the catalysts. CuO/CeO2/MnOx/Al2O3 (30/40/20/10) catalyst exhibited a good activity and a good selectivity that was comparable with CuO/CeO2 and 10% CuO/Ce1-xMnxO2, and can handle high-capacity gas. The activity and selectivity of catalysts decrease in the presence of CO2 and H2O, but it still showed good stability. It is a practical and ideal catalyst for PROX reaction.
    显示于类别:[化學工程與材料工程研究所] 博碩士論文

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