首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Three-dimensional Pd/Pt bimetallic nanodendrites on a highly porous copper foam fiber for headspace solid-phase microextraction of BTEX prior to their quantification by GC-FID
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Three-dimensional Pd/Pt bimetallic nanodendrites on a highly porous copper foam fiber for headspace solid-phase microextraction of BTEX prior to their quantification by GC-FID

机译:高孔铜泡沫纤维上的三维Pd / Pt双金属纳米纤维,用于通过GC-FID定量的BTEX前空间固相微萃取

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摘要

The preparation of bimetallic Pd/Pt nanofoam for use in fiber based solid-phase microextraction (SPME) is described. First, a highly porous copper foam was prepared on the surface of an unbreakable copper wire by an electrochemical method. Then, the substrate was covered with metallic Pd and Pt using galvanic replacement of the Cu nanofoam substrate by applying a mixture of Pd(II) and Pt(IV) ions. The procedure provided an efficient route to modify Pd/Pt nanofoams with large specific surface and low loading with expensive noble metals. The fiber was applied to headspace SPME of benzene, toluene, ethylbenzene and xylene (BTEX) (as the model compounds) in various spiked water and wastewater samples. It was followed by gas chromatography-flame ionization detection (GC-FID). A Plackett-Burman design was performed for screening the experimental factors prior to Box-Behnken design. Compared with the commercial PDMS SPME fiber (100m), it had higher extraction efficiency for BTEX. Under the optimum conditions, the method has low limits of detection (0.16-0.35gL(-1)), a wide linear range (1-200gL(-1)), relative standard deviations between 5.8 and 10.5%, and good recoveries (85% from spiked samples).
机译:描述了用于纤维基固相微萃取(SPME)的双金属Pd / Pt纳米泡沫的制备。首先,通过电化学方法在不可用铜线的表面上制备高度多孔的铜泡沫。然后,通过施加Pd(II)和Pt(IV)离子的混合物,用金属pd和Pt覆盖金属Pd和Pt。该方法提供了一种有效的途径,用于改变具有大的比表面积和低负载的Pd / Pt纳米泡沫,昂贵的贵金属。将纤维施用于各种尖刺水和废水样品中的苯,甲苯,乙苯和二甲苯(BTEX)(作为模型化合物)的顶空SPME。其次是气相色谱 - 火焰电离检测(GC-FID)。在Box-Behnken设计之前进行Plackett-Burman设计,用于筛选实验因素。与商业PDMS SPME纤维(100M)相比,对BTEX具有更高的提取效率。在最佳条件下,该方法具有低的检测限(0.16-0.35gL(-1)),宽线性范围(1-200gL(-1)),相对标准偏差在5.8%和10.5%之间,良好的回收率( & 85%来自尖刺样品)。

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