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Facile preparation of cuprous oxide decorated mesoporous carbon by one-step reductive decomposition for deep desulfurization

机译:一步还原还原深度脱硫轻松制备氧化亚铜修饰的介孔碳

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摘要

Deep desulfurization of fossil fuels has always been an urgent demand for environmental protection in fossil energy utilization. So, developing simple preparation method for adsorbents with high activity and low cost is always the goal of adsorption desulfurization. Cu-based materials are attractive pi-complexation adsorbents owing to their high-cost performance. Here we report the fabrication of cuprous oxide-modified mesoporous carbon by a one-step thermal treatment at relatively low temperatures. In this method, the mesoporous carbon not only provides a stable platform but also acts as a reducing agent to promote the reaction of the Cu precursor. The impregnated Cu(NO3)(2) precursor was transformed to the cuprous oxide by carbon-assisted reduction and decomposition at a much lower temperature (below 300 degrees C) without the requirement for an additional reducing agent. The resulting Cu2O-functionalized mesoporous carbon exhibited high surface area with 567 m(2) g(-1) and the benzothiophene capture ability reach 0.47 mmol g(-1), which is significantly greater than those reported for Cu2O-modified mesoporous silicas. Furthermore, the majority of the adsorptive desulfurization of this material could be recovered over 90% after five recycling trials. This strategy has three advantages: one-step preparation at low temperatures, a high desulfurization capacity, and good reusability.
机译:化石燃料的深度脱硫一直是化石能源利用中环境保护的迫切需求。因此,开发一种高活性,低成本的吸附剂的简单制备方法一直是吸附脱硫的目标。铜基材料由于其高性价比而成为有吸引力的pi络合吸附剂。在这里,我们报告了在相对较低的温度下通过一步热处理制备氧化亚铜改性的介孔碳的方法。在这种方法中,中孔碳不仅提供了稳定的平台,而且还充当了促进铜前体反应的还原剂。浸渍的Cu(NO3)(2)前驱物通过碳辅助还原和分解,在更低的温度(低于300摄氏度)下转化为氧化亚铜,而无需使用其他还原剂。所得的Cu2O官能化的介孔碳表现出高表面积,为567 m(2)g(-1),苯并噻吩的捕获能力达到0.47 mmol g(-1),明显大于报告的Cu2O改性的介孔二氧化硅。此外,经过五次循环试验,该材料的大部分吸附脱硫可回收90%以上。该策略具有三个优点:在低温下一步制备,高脱硫能力和良好的可重复使用性。

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