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首页> 外文期刊>Science >CATALYTIC CLEAVAGE OF THE C-H AND C-C BONDS OF ALKANES BY SURFACE ORGANOMETALLIC CHEMISTRY - AN EXAFS AND IR CHARACTERIZATION OF A ZR-H CATALYST
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CATALYTIC CLEAVAGE OF THE C-H AND C-C BONDS OF ALKANES BY SURFACE ORGANOMETALLIC CHEMISTRY - AN EXAFS AND IR CHARACTERIZATION OF A ZR-H CATALYST

机译:表面有机金属化学催化裂解炔烃的C-H和C-C键-ZR-H催化剂的透水和红外表征

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摘要

The catalytic cleavage under hydrogen of the C-H and C-C bonds of alkanes with conventional catalysts requires high temperatures. Room-temperature hydrogenolysis of simple alkanes is possible on a well-defined and well-characterized zirconium hydride supported on silica obtained by surface organometallic chemistry. The surface structure resulting from hydrogenolysis of (=SiO)Zr(Np)(3) (Np, neopentyl) was determined from the extended x-ray absorption fine structure (EXAFS) and H-1 and Si-29 solid-state nuclear magnetic resonance and infrared (IR) spectra. A mechanism for the formation of (=SiO)(3)Zr-H and (=SiO)(2)SiH2 and the resulting low-temperature hydrogenolysis of alkanes is proposed. The mechanism may have implications for the catalytic formation of methane, ethane, and lower alkanes in natural gas.
机译:用常规催化剂在氢的催化下烷烃的C-H和C-C键的裂解需要高温。在由表面有机金属化学方法制得的二氧化硅上负载的定义明确且特征明确的氢化锆上,可以进行简单烷烃的室温氢解。由扩展X射线吸收精细结构(EXAFS)以及H-1和Si-29固态核磁确定了由(= SiO)Zr(Np)(3)(Np,新戊基)氢解产生的表面结构共振和红外(IR)光谱。提出了形成(= SiO)(3)Zr-H和(= SiO)(2)SiH2以及由此产生的烷烃低温氢解反应的机理。该机制可能对天然气中甲烷,乙烷和低级烷烃的催化形成有影响。

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