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EVOLUTION OF THE Cu/ZnO METHANOL SYNTHESIS CATALYST DURING ITS REDUCTION AND RE-OXIDATION

机译:还原/再氧化过程中Cu / ZnO甲醇合成催化剂的演变

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Cu K EXAFS studies of the structure of Cu-Zn oxide catalyst were performed for the as prepared samples,those after its activation by hydrogen and after its subsequent re-oxidation.It was found that during the primary formation of the CuZnO solid solution,the copper ions are dissolved in the extended stacking faults of the ZnO lattice as ultra-small oxide clusters.Activation by hydrogen at 473 K leads to the reduction of most copper cations to Cu~0 with the formation of nanoparticles with the characteristic size of ca.1.6 nm.The copper metal particles were re-oxidized to Cu~(2+) at 523 K in a helium flow containing 0.05 vol.% oxygen.The re-oxidized cations do not form a CuO phase.Instead,they return to the extended stacking faults of ZnO.However,this time they form stripe-like clusters of square-planar coordinated copper cations.
机译:对Cu-Zn氧化物催化剂的结构进行了Cu K EXAFS研究,制备的样品经氢活化后再进行再氧化。发现在CuZnO固溶体的初步形成过程中,铜离子以超小氧化物簇的形式溶解在ZnO晶格的扩展堆垛层错中。氢在473 K下的活化导致大多数铜阳离子还原为Cu〜0,并形成了特征尺寸约为ca. 1.6 nm。在523 K的氦气中,铜金属颗粒在含0.05 vol。%氧气的氦气流中重新氧化为Cu〜(2+)。重新氧化的阳离子不形成CuO相,而是返回到延长了ZnO的堆垛层错。但是,这一次它们形成了正方形平面配位铜阳离子的条状簇。

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