Infra-red study of hydrogen chloride adsorption on rutile surfaces

G. D. Parfitt, J. Ramsbotham, C. H. Rochester
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引用次数: 27

Abstract

The adsorption of hydrogen chloride on outgassed, deuterated, and reduced rutile surfaces has been studied by infra-red spectroscopy. Surface Ti4+O2–Ti4+ groups react with hydrogen chloride to form hydroxide ions and chloride ions on adjacent titanium ion sites. The reaction of hydrogen chloride with surface hydroxide ions leads to water coordinately bound to Ti4+ and associated with a chloride ion. Rearrangement to Ti4+Cl– species occurs and leads to the formation of adsorbed water which can react with hydrogen chloride to form H3O+Cl– on the surface. The adsorption of hydrogen chloride leads to surface species which act as Bronsted acid sites in the presence of adsorbed ammonia or pyridine.
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金红石表面氯化氢吸附的红外研究
用红外光谱法研究了氯化氢在脱气、氘化和还原金红石表面的吸附。表面Ti4+ O2-Ti4 +基团与氯化氢反应,在相邻的钛离子位点上形成氢氧化物离子和氯离子。氯化氢与表面氢氧化物离子的反应使水与Ti4+配位结合,并与氯离子结合。发生Ti4+Cl -的重排,形成吸附水,吸附水可与氯化氢反应,在表面形成h30 +Cl -。氯化氢的吸附导致表面物质在吸附氨或吡啶的存在下充当Bronsted酸位点。
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