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Synthesis and characterization of supported polysugar-stabilized palladium nanoparticle catalysts for enhanced hydrodechlorination of trichloroethylene

机译:负载型糖稳定钯纳米颗粒催化剂的增强三氯乙烯加氢脱氯反应

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摘要

Palladium (Pd) nanoparticle catalysts were successfully synthesized within an aqueous phase using sodium carboxymethyl cellulose (CMC) as a capping ligand which offers a green alternative to conventional nanoparticle synthesis techniques. The CMC-stabilized Pd nanoparticles were subsequently dispersed within support materials using the incipient wetness impregnation technique for utilization in heterogeneous catalyst systems. The unsupported and supported (both calcined and uncalcined) Pd nanoparticle catalysts were characterized using transmission electron microscopy, energy dispersive x-ray spectrometry, x-ray diffraction, and Brunauer-Emmett-Teller surface area measurement and their catalytic activity toward the hydrodechlorination of trichloroethylene (TCE) in aqueous media was examined using homogeneous and heterogeneous catalyst systems, respectively. The unsupported Pd nanoparticles showed considerable activity toward the degradation of TCE, as demonstrated by the reaction kinetics. Although the supported Pd nanoparticle catalysts had a lower catalytic activity than the unsupported particles that were homogeneously dispersed in the aqueous solutions, the supported catalysts retained sufficient activity toward the degradation of TCE. In addition, the use of the hydrophilic Al _2O _3 support material induced a mass transfer resistance to TCE that affected the initial hydrodechlorination rate. This paper demonstrates that supported Pd catalysts can be applied to the heterogeneous catalytic hydrodechlorination of TCE.
机译:使用羧甲基纤维素钠(CMC)作为封端配体,成功地在水相中合成了钯(Pd)纳米颗粒催化剂,这为常规纳米颗粒合成技术提供了绿色替代方案。随后使用初期湿润浸渍技术将CMC稳定的Pd纳米颗粒分散在载体材料中,以用于非均相催化剂体系。使用透射电子显微镜,能量色散X射线光谱法,X射线衍射和Brunauer-Emmett-Teller表面积测量来表征未负载和负载的(煅烧和未煅烧的)Pd纳米颗粒催化剂及其对三氯乙烯加氢脱氯的催化活性。分别使用均相和非均相催化剂体系检查了水性介质中的三氯乙烷(TCE)。如反应动力学所证明,未负载的Pd纳米颗粒对TCE的降解表现出相当大的活​​性。尽管负载的Pd纳米颗粒催化剂的催化活性比均匀分散在水溶液中的未负载的颗粒低,但负载的催化剂对TCE的降解保持了足够的活性。另外,使用亲水性Al _2O _3载体材料引起了对TCE的传质阻力,从而影响了初始加氢脱氯速率。本文证明了负载型钯催化剂可用于三氯乙烯的多相催化加氢脱氯。

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