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Promotion Effect of Ga-Co Spinel Derived from Layered Double Hydroxides for Toluene Oxidation

机译:Ga-Co尖晶石衍生自层双氢氧化硅氧烷的促进作用,用于甲苯氧化

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摘要

Considering the radius similarity of Al3+ (0.50 angstrom) and Ga3+ (0.62 angstrom), Al-Co and Ga-Co layered double hydroxides (LDH) was prepared as precursor to improve the synergetic interaction of the transition metals. The Al-Co and Ga-Co spinel catalysts were obtained by the following calcination for the toluene oxidation. The Ga-Co (E-a=79.5 kJ mol(-1)) showed higher activity than the Al-Co (E-a=95.4 kJ mol(-1)), and it exhibited excellent stability and resistance to carbon deposition during a 50 h reaction period at 300 degrees C. Characterization results indicated that the improved activity of Ga-Co spinel could be attributed to the higher reducibility (H-2-TPR), more surface Co3+ and adsorbed oxygen in quantity (XPS) and adsorbed toluene (Toluene-TPD) than Al-Co spinel. Compared with traditional Ga-Co binary catalyst, the spinel structure possessed more B-sites cations outermost of the surface and surface oxygen vacancies for the toluene adsorption and ring-open reaction.
机译:考虑到Al3 +(0.50埃)和Ga3 +(0.62埃),Al-Co和Ga-Co层层双氢氧化物(LDH)的半径相似度被制备为前体,以改善过渡金属的协同相互作用。 通过以下煅烧得到甲苯氧化的Al-Co和Ga-Co尖晶石催化剂。 GA-CO(EA = 79.5kJMol(-1))显示比Al-Co更高的活性(EA = 95.4 kJ摩尔(-1)),并且在50h反应期间表现出优异的稳定性和对碳沉积的耐碳沉积 在300℃下的时间。表征结果表明,Ga-Co尖晶石的改善活性可归因于较高的再还原性(H-2-TPR),更多的表面CO3 +和量的量(XPS)和吸附的甲苯(甲苯 - TPD)比Al-Co Spinel。 与传统的GA-CO二元催化剂相比,尖晶石结构具有更多的B场阳离子的表面和表面氧空位,用于甲苯吸附和环开反应。

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