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americanyk

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ccshiyu(½ð±Ò+3):¸Ðл°æÖ÷µÄÏêϸ»Ø¸´ 2010-06-02 22:37:36
liconglin970410(½ð±Ò+1):¶àлָµã£¬»¶Ó­³£À´½»Á÷ 2010-06-08 13:50:33
tangjy(½ð±Ò+1):лл»ØÌû½»Á÷ 2010-10-19 14:13:32
[quote]Originally posted by ccshiyu at 2010-06-02 08:26:06:

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Depend on the conditions. The bond is noramlly weak.
4Â¥2010-06-02 18:40:27
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ccshiyu

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3Â¥2010-06-02 15:55:51
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yingguang

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herl24

Òø³æ (ÕýʽдÊÖ)

ÒýÓûØÌû:
Originally posted by americanyk at 2010-06-02 18:40:27:
[quote]Originally posted by ccshiyu at 2010-06-02 08:26:06:

1.½ðÊôÑõ»¯Îï±íÃæµÄôÇ»ùÊǽðÊôÇâÑõ»¯Îï¸ßαºÉÕÍÑË®Ðγɵģ¿»¹ÊǽðÊôÑõ»¯ÎïÎü¸½¿ÕÆøÖеÄË®·Ö×ÓÐγɵģ¿»¹ÊÇÁ½Õß¶¼ÓУ¿
Answer: ½ðÊôÑõ»¯ ...

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8Â¥2010-10-19 10:57:24
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jinkai838

ľ³æ (ÖøÃûдÊÖ)

Surface Oxide¡ªSupport Interactions in the Molecular Design of Supported Metal Oxide Selective Oxidation Catalysts
A series of metal oxides were deposited on the surface of different oxide supports to study the surface oxide - support interactions. The dehydrated Raman spectra of the supported metal oxide catalysts reveal the presence and structure of the supported metal oxide phases. The same surface metal oxide species were found on the different oxide supports for each of the supported metal oxide systems. The reactivity of the surface metal oxide species, however, depends on the specific oxide support (TiO2~ZrO2>Nb2O5>Al2O3~SiO2). For a given oxide support, the reactivity depends on the specific surface metal oxide species (e.g. V0x > MoOy). The redox activation energy for all the surface metal oxide phases lie in the range of 18-22 kcal/mole. The similar activation energies suggests that the number of active sites and/or the activity per site is responsible for the difference in reactivity. The redox TON for the methanol oxidation reaction correlates with the reduction temperature during TPR experiments, which suggests that the bridging M-O-Support bond controls the activity during redox reactions.
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9Â¥2010-10-19 14:45:07
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jinkai838

ľ³æ (ÖøÃûдÊÖ)

Israel Wachs

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G. Whitney Snyder Professor and Professor of Chemical Engineering
Director, Operando Molecular Spectroscopy and Catalysis Research Lab

Ph.D. Stanford University, 1977
M.S. Stanford University, 1974
B.E. City College of New York, 1973

Our research focuses on surface oxides and has demonstrated that, for many two-component metal oxide systems, one metal oxide may be present as an atomically dispersed phase over a second metal oxide substrate. The state of the atomically dispersed metal oxide, the surface oxide, has a different structure from that of its bulk unsupported oxide counterpart. This structural difference usually results in very different chemical properties. Our studies have shown that a relationship exists between the metal oxide structure and its surface reactivity (reduction properties and catalytic activity or selectivity).

The complex structures of the atomically dispersed surface oxides are poorly understood. The focus of our program is therefore to examine systematically the various structures of these atomically dispersed surface oxides on oxide substrates and to determine the factors that control the metal oxide structure. Much of the structural information about surface oxides can be provided with modern laser Raman spectroscopy because of the dependence of the Raman spectrum on the structure of the scattering material.

Another of our goals is to define the relationship between surface oxide structures and their various physical and chemical properties. A better understanding of the synthesis and materials science/solid-state chemistry of the surface oxides is also emerging from this research program. The insight generated from this research has implications for metal oxide catalysts, ceramic materials, pigment materials, and electronic devices which find wide application in the pollution control industry, chemical industry, petroleum industry and the advanced materials industries
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10Â¥2010-10-19 14:49:45
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