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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Nanostructured molybdenum oxide in a 3D metal organic framework and in a 2D polyoxometalate network for extraction of chlorinated benzenes prior to their quantification by GC-MS
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Nanostructured molybdenum oxide in a 3D metal organic framework and in a 2D polyoxometalate network for extraction of chlorinated benzenes prior to their quantification by GC-MS

机译:3D金属有机框架中的纳米结构氧化钼和在2D多氧化术网络中,用于通过GC-MS定量提取氯化苯

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摘要

A three-dimensional metal organic framework (3D-MOF) and a two-dimensional polyoxometalate (2D-POM), both incorporating nanostructured molybdenum (VI) oxide, were synthesized and implemented for headspace needle trap extraction of traces of chlorobenzenes (CBs). The 3D-MOF of type {(Mo2O6)(4,4-bpy)}(n) and the 2D-POM of type [4,4-bpy][Mo7O22] were synthesized by a solvothermal process and characterized by FT-IR, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermogravimetry, energy dispersive X-ray, elemental mapping and Brunner-Emmet-Teller adsorption analyses. The 3D-MOF proved to be superior. Following thermal desorption, the CBs (monochlorobenzene, 1,4-dichlorobenzene, 1,2-dichlorobenzene, 1,2,4-trichlorobenzene and 1,2,3,4-tetrachlorobenzene) were quantified by GC-MS. Under optimized conditions, the calibration plots are linear in the 1-1000ng.L-1 concentration range, and the limits of detection range from 0.2 to 2ng.L-1. The intra- and inter-day relative standard deviations for three replicates at levels of 10 and 200ng.L-1 are in the range of 5-12% and 10-15%, respectively. The needle-to-needle reproducibility was also found to be in the range of 6-13%. The application of the method to the analysis of various spiked real water samples resulted in recoveries between 84 and 114%.
机译:三维金属有机框架(3D-MOF)和二维多氧化酯酸盐(2D-POM)掺入纳米结构钼(VI)氧化物,并用于氯苯痕量的顶空针捕集捕获萃取。通过溶剂热法合成{(MO2O6)(4,4-BPY)(4,4-BPY)(4,4-BPY)}(N)和2D-POM的3D-MOF和[4,4-BPY] [MO7O22]的2D-POM,并通过FT-IR表征,粉末X射线衍射,扫描电子显微镜,透射电子显微镜,热重度,能量分散X射线,元素映射和Brunner-Emmet-exers吸附分析。 3D-MOF被证明是优越的。通过GC-MS量化热解吸后,CBS(二氯苯,1,4-二氯苯,1,2-二氯苯,1,2,3,4-四氯苯和1,2,3,4-四氯苯)。在优化条件下,校准图在1-1000ng.L-1浓度范围内是线性的,并且检测范围为0.2至2ng.l-1。在10和200ng.L-1水平的三种重复的日内相对标准偏差分别为5-12%和10-15%。针对针头再现性也被发现在6-13%的范围内。该方法在分析各种尖刺实水样中的应用导致回收率为84至114%。

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