Ko Eun-Yong, Park Eun Duck, Seo Kyung Won, Lee Hyun Chul, Lee Doohwan, Kim Soonho
Department of Chemical Engineering, Division of Chemical Engineering and Materials Engineering, Ajou University, Wonchun-Dong Yeongtong-Gu Suwon, 443-749, Republic of Korea.
J Nanosci Nanotechnol. 2006 Nov;6(11):3567-71.
The preferential CO oxidation in the presence of excess hydrogen was studied over Pt-Co/gamma-Al2O3. CO chemisorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectrometer (EDX) and temperature programmed reduction (TPR) were conducted to characterize active catalysts. The catalytic activity for CO oxidation and methanation at low temperatures increased with the amounts of cobalt in Pt-Co/gamma-Al2O3. This accompanied the TPR peak shift to lower temperatures. The optimum molar ratio between Co and Pt was determined to be 10. The co-impregnated Pt-Co/gamma-Al2O3 appeared to be superior to Pt/Co/gamma-Al2O3 and Co/Pt/gamma-Al2O3. The reductive pretreatment at high temperature such as 773 K increased the CO2 selectivity over a wide reaction temperature. The bimetallic phase of Pt-Co seems to give rise to high catalytic activity in selective oxidation of CO in H2-rich stream.
研究了在过量氢气存在下,Pt-Co/γ-Al₂O₃ 上的优先 CO 氧化反应。进行了 CO 化学吸附、X 射线衍射(XRD)、透射电子显微镜(TEM)、能量色散 X 射线光谱仪(EDX)和程序升温还原(TPR)来表征活性催化剂。Pt-Co/γ-Al₂O₃ 中 CO 氧化和低温甲烷化的催化活性随钴含量的增加而提高。这伴随着 TPR 峰向低温移动。Co 与 Pt 的最佳摩尔比确定为 10。共浸渍的 Pt-Co/γ-Al₂O₃ 似乎优于 Pt/Co/γ-Al₂O₃ 和 Co/Pt/γ-Al₂O₃。在 773 K 等高温下进行的还原预处理在较宽的反应温度范围内提高了 CO₂ 选择性。Pt-Co 的双金属相似乎在富氢气流中 CO 的选择性氧化中产生了高催化活性。