Oxidation of S at Fe metal and oxide surfaces and interfaces

被引:19
作者
Cabibil, H [1 ]
Kelber, JA [1 ]
机构
[1] UNIV N TEXAS,DEPT CHEM,DENTON,TX 76203
关键词
auger electron spectroscopy; iron; oxidation; sulphides; thermal desorption spectroscopy;
D O I
10.1016/S0039-6028(96)01169-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Temperature-programmed desorption (TPD) and Auger electron spectroscopy (AES) were used to study the interactions of H2S and S adsorbed on oxidized Fe and metallic Fe surfaces, in the presence of H2O or O-2 vapor. Our results reveal contrasting chemical behavior between adsorbed S on a clean Fe(poly) metal surface and adsorbed S on an Fe oxide surface. SO2 formation occurs at the Fe oxide surface due to a reaction between adsorbed S and H2O or O-2 vapor. On the Fe(poly) metal surface, no such SO2 formation was observed. The chemical behavior of S located at the metal-oxide interface was also investigated. Our results demonstrate the deleterious effect of S when present at the metal-oxide interface. S located at the metal-oxide interface reacts with the oxide to form SO2. This SO2 formation results in destruction of metal-oxide bonds at the interface and causes oxide destabilization with consequent detachment of the oxide from the metal In contrast to the interfacial S, S adsorbed on the oxide surface does not form SO2 under UHV conditions. SO2 formation on the oxide surface occurs only in the presence of H2O or O-2 vapor. In addition, some degradation of an oxide was observed due to S deposited on top of the oxide surface. Our results indicate that the initial adsorption site of the S atom (metal versus oxide) exerts a critical influence on subsequent oxidation chemistry. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:257 / 274
页数:18
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