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Efficient transformation in characteristics of cations supported-reduced graphene oxide nanocomposites for the destruction of trichloroethane

机译:阳离子负载还原氧化石墨烯纳米复合材料特性的高效转化以破坏三氯乙烷

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摘要

Experiments were conducted to investigate the use of graphene-oxide supported metallic nanocomposites for improving the degradation of trichloroethane (TCA) by sodium percarbonate (SPC). Two methods of production, chemical reduction (CR) and solvo-thermal (ST), were tested for preparation of single (Fe) and binary (Fe-Cu) nanocomposites supported by reduced graphene oxide (rGO). A variety of analytical techniques including N2 adsorption Brunauer-Emmett-Teller (BET), x-ray diffraction (XRD), fourier-transfrom infrared spectroscopy (FTIR), and transmisison electron microscopy (TEM) were applied to characterize the physicochemical and microstructural properties of the synthesized nanocomposites. The characterization indicated that the CR method produced nanocomposites that comprised only mesoporous structure. Conversely, both micro and mesoporous structures were present for samples produced with the ST method. The synthesized single and bimetallic composites produced from the ST method showed higher surface areas, i.e. 93.6 m2/g and 119.2 m2/g as compared to the ones synthesized via the CR method, i.e. 13.8 m2/g and 38.0 m2/g respectively. The results of FTIR and XRD analyses confirmed that the ST method produced highly crystalline nanocomposites. SEM and TEM analysis validated that metallic particles with definite morphology well distributed on the surface of rGO. X-ray photoelectron spectroscopy (XPS) analysis confirmed the homogeneity nanocomposites and occurrence of variation in copper oxidation states during degradation process. EDS mapping validate the homogeneous distribution of Cu and Fe at reduced graphene oxide surface. The Fe-Cu/rGO (ST) activated SPC system effectively degraded TCA (92%) in 2.5 h at low nanocomposite dose compared to the Fe-Cu/rGO (CR) and only Fe, for which the maximum degradation efficiencies achieved were 81% and 34%. In conclusion, excellent catalytic characteristics were observed for the ST-synthesized single and bimetallic (Fe/rGO, Fe-Cu/rGO) catalysts. These catalysts were successful in improving the degradation of TCA via activated SPC.
机译:进行实验以研究使用氧化石墨烯负载的金属纳米复合材料改善过碳酸钠(SPC)对三氯乙烷(TCA)的降解。测试了两种生产方法:化学还原(CR)和溶剂热(ST),以制备由还原氧化石墨烯(rGO)支撑的单一(Fe)和二元(Fe-Cu)纳米复合材料。包括N2吸附Brunauer-Emmett-Teller(BET),X射线衍射(XRD),傅立叶变换红外光谱(FTIR)和透射电子显微镜(TEM)在内的多种分析技术用于表征理化和微观结构性质合成的纳米复合材料。表征表明,CR法产生仅包含中孔结构的纳米复合材料。相反,通过ST方法生产的样品同时存在微孔结构和中孔结构。用ST法制得的合成的单金属和双金属复合材料的表面积比通过水合物合成的表面积高,分别为93.6 m 2 / g和119.2 m 2 / g。 CR方法,分别为13.8 m 2 / g和38.0 m 2 / g。 FTIR和XRD分析的结果证实了ST方法产生了高度结晶的纳米复合材料。 SEM和TEM分析证实,具有一定形态的金属颗粒在rGO表面上分布良好。 X射线光电子能谱(XPS)分析证实了降解过程中纳米复合材料的均一性和铜氧化态的变化。 EDS映射验证了还原的氧化石墨烯表面上Cu和Fe的均匀分布。 Fe-Cu / rGO(ST)活化的SPC系统与Fe-Cu / rGO(CR)和仅铁相比,在低纳米复合剂量下可在2.5小时内有效降解三氯乙酸(92%),而实现最大降解效率为81 %和34%。总之,对于ST合成的单金属和双金属(Fe / rGO,Fe-Cu / rGO)催化剂,观察到了优异的催化特性。这些催化剂通过活化的SPC成功地改善了TCA的降解。

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