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Design of catalysts with artificially controllablefuntions using surface acoustic waves and resonance oscillations generated on ferroelectric materials

机译:使用表面声波和铁电材料产生的谐振振荡催化剂设计催化剂的设计

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A poled ferroelectric material of a LiNbO_3 single crystal and a polycrystalline lead strontium zirconium titanate(PSZT) disc were employed as a catalyst substrate, on which various metals such as Pd, Ag, Ni and Pt and a WO_3 oxide were deposited as a thin film catalyst. The effects of acoustic waves generated by rf power upon catalyst activation and reaction selectivity have been examined. The activity for Co oxidation of a Pt/PSZT catalyst increased by a factor of 3.9 with a radial-extensional (RE) mode. The activation energy of the reaction was larger for the TE mode(38 kJmol~(-1)) than that for the RE mode(24 kJmol~(-1)). The polarization axis-dependent changes in surface potential occurred with the TE mode, but not with the RE mode. With the TE mode, the activation energy of ethanol oxidation over a Ni/LiNbO_3 and a Ag/LiNbO_3 catalyst decreased from 36 to 19 kJmol~(-1) and from 76 to 30 kJmol~(-1), respectively, and the TE mode had a larger effect on the reaction with a higher activation energy. In ethanol dehydrogenation and dehydration on a WO_3 / LiNbO_3 catalyst, the TE mode increased remarkably the selectivity for ethylene production without giving a significant change to acetaldehyde production. The effects of acoustic wave excitations on the catalysts are discussed.
机译:甲极化的铌酸锂单晶的铁电体材料和钛酸多晶铅锶锆(PSZT)盘被用作催化剂基质,在其上的各种金属,如钯,银,Ni和Pt和一个WO_3氧化物沉积为薄膜催化剂。已经检验通过在催化剂的活化和反应选择性的射频功率产生的声波的影响。对于在Pt / PSZT催化剂的CO氧化活性与径向伸展(RE)模式增加了3.9倍。该反应的活化能是为TE模式(38 kJmol〜(-1))比用于RE模式的情况下(24 kJmol〜(-1))。表面电位的偏振轴依赖性变化发生与TE模,但不与RE模式。与TE模式,乙醇氧化的在镍/铌酸锂和银/铌酸锂催化剂的活化能降低36至19 kJmol〜(-1),并从76至30 kJmol〜(-1)分别和TE模式对具有更高活化能的反应的更大的效果。在乙醇脱氢和脱水在WO_3 /铌酸锂催化剂,TE模式显着地增加用于乙烯生产的选择性而不给予乙醛生产显著变化。讨论的催化剂声波激励的效果。

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