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In situ investigation of solid-liquid catalytic interfaces by attenuated total reflection infrared spectroscopy

机译:衰减全反射红外光谱原位研究固液催化界面

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It is demonstrated that attenuated total reflection infrared (ATR-IR) spectroscopy can be effectively used for in situ investigation of supported catalyst-liquid interfaces. Thin (ca. 10 mum) films of a 5 wt % Pt/gamma-Al2O3 catalyst were deposited onto the surface of a germanium waveguide. The very small support particles (average size, 37 nm) form a stable film that does not peel from the waveguide when exposed to flowing liquid. The catalyst film is thick enough so that essentially all of the IR electric field is attenuated within the film thus decreasing bulk liquid signals. The applicability of this technique for studying adsorption and reaction of molecules on supported catalysts has been tested using several probe molecules (carbon monoxide, formaldehyde, ethanol, butyronitrile) and solvents (water, ethanol, hexane). Examination of adsorption of CO from aqueous and ethanolic solutions reveals that CO resides in both atop and bridged configurations on the catalyst surface in both solvents. A 10-fold decrease in the oxidation rate of adsorbed CO in ethanol was observed. This is attributed both to the lower solubility of O-2 in ethanol compared to water and the likely presence of trace ethanol dissociation products that may block O(2)2 adsorption. The dissociation of formaldehyde and ethanol in water was studied by following the formation of adsorbed CO. The extent of dissociation appeared considerably larger for formaldehyde than for ethanol as determined by comparing absorption intensities and peak frequencies. Finally, adsorption of butyronitrile from hexane was examined with a view toward extending this approach to the study of more complex systems. Butyronitrile was found to adsorb on the catalyst by sigma-bonding of the CN group with the platinum. The prospects of using this approach to examine solid-catalyzed liquid-phase reactions are discussed in light of these findings. [References: 45]
机译:结果表明,衰减全反射红外(ATR-IR)光谱可以有效地用于负载催化剂-液体界面的原位研究。将5 wt%Pt /γ-Al2O3催化剂的薄膜(约10微米)沉积在锗波导的表面上。非常小的支撑颗粒(平均尺寸为37 nm)形成稳定的膜,当暴露于流动的液体中时不会从波导上剥离。催化剂膜足够厚,以使膜内的所有IR电场都基本衰减,从而降低了整体液体信号。已经使用几种探针分子(一氧化碳,甲醛,乙醇,丁腈)和溶剂(水,乙醇,己烷)测试了该技术在研究负载型催化剂上分子的吸附和反应方面的适用性。从水溶液和乙醇溶液中吸附CO的研究表明,在两种溶剂中,CO均以顶部和桥接构型存在于催化剂表面。观察到乙醇中吸附的CO的氧化速率降低了10倍。这既归因于O-2在乙醇中的溶解度低于水,又归因于痕量乙醇解离产物的存在,可能会阻止O(2)2吸附。通过跟踪吸附的CO的形成来研究甲醛和乙醇在水中的离解。通过比较吸收强度和峰值频率,甲醛的离解程度似乎比乙醇大。最后,检查了丁腈从己烷中的吸附,以期将这种方法扩展到研究更复杂的系统。发现丁腈通过CN基团与铂的σ键结合而吸附在催化剂上。鉴于这些发现,讨论了使用这种方法检查固相催化液相反应的前景。 [参考:45]

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