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In situ FTIR study on the formation and adsorption of CO on alumina-supported noble metal catalysts from H2 and CO2 in the presence of water vapor at high pressures

机译:在高压水蒸气存在下,H2和CO2在氧化铝负载的贵金属催化剂上形成和吸附CO的原位FTIR研究

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摘要

The formation and adsorption of CO from CO2 and H2 at high pressures were studied over alumina-supported noble metal catalysts (Pt, Pd, Rh, Ru) by in situ FTIR measurements. To examine the effects of surface structure of supported metal particles and water vapor on the CO adsorption, FTIR spectra were collected at 323 K with untreated and heat (673 K) treated catalysts in the absence and presence of water (H2O, D2O). It was observed that the adsorption of CO occurred on all the metal catalysts at high pressures, some CO species still remained adsorbed under ambient conditions after the high pressure FTIR measurements, and the frequencies of the adsorbed CO species were lower either for the heat treated samples or in the presence of water vapor. It is assumed that the CO absorption bands on atomically smoother surfaces appear at lower frequencies and that water molecules are adsorbed more preferentially on atomically rough surfaces rather than CO species.
机译:通过原位FTIR测量研究了在氧化铝负载的贵金属催化剂(Pt,Pd,Rh,Ru)上,高压下CO2和H2中CO的形成和吸附。为了检查负载的金属颗粒和水蒸气的表面结构对CO吸附的影响,在不存在和存在水(H2O,D2O)的情况下,未经处理和热处理(673 K)的催化剂在323 K下收集FTIR光谱。观察到在高压下所有金属催化剂上都发生了CO的吸附,在高压FTIR测量之后,一些CO物种在环境条件下仍然保持吸附,并且对于热处理的样品,吸附的CO物种的频率均较低。或在水蒸气存在下。假定在原子较光滑的表面上的CO吸收带以较低的频率出现,并且水分子更优先地吸附在原子粗糙的表面而不是CO物种上。

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