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首页> 外文期刊>Analytical and bioanalytical chemistry >Oxidized single-walled carbon nanohorns as sorbent for porous hollow fiber direct immersion solid-phase microextraction for the determination of triazines in waters
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Oxidized single-walled carbon nanohorns as sorbent for porous hollow fiber direct immersion solid-phase microextraction for the determination of triazines in waters

机译:氧化单壁碳纳米角作为多孔中空纤维直接浸没固相微萃取的吸附剂,用于测定水中的三嗪

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摘要

This paper evaluates the potential of oxidized single-walled carbon nanohorns (o-SWNHs) immobilized on the pores of a hollow fiber (HF) for the direct immersion solid-phase microextraction of triazines from waters. The fabrication of the device requires the oxidation of the nanoparticles by means of microwave irradiation in order to obtain a homogeneous dispersion in methanol. Then, a porous hollow fiber is immersed in the methanolic dispersion of the o-SWNHs under ultrasound stirring. This procedure permits the immobilization of the o-SWNHs in the pores of the hollow fiber. For the extraction, a stainless steel wire was introduced inside the fiber to allow the vertical immersion of the o-SWNHs-HF in the aqueous standard/water sample. The triazines were preconcentrated on the immobilized o-SWNHs and further eluted using 150 μL of methanol. The solvent was evaporated and the residue reconstituted in 10 μL of methanol for sensitivity enhancement. Gas chromatography-mass spectrometry was selected as instrumental technique. The limits of detection were between 0.05 and 0.1 μg L~(-1) with an excellent precision (expressed as relative standard deviation) between runs (below 10.2 %) and between fibers (below 12.8 %). Finally, the method was applied to the determination of the triazines in fortified waters, an average recovery value of 90 % being obtained.
机译:本文评估了固定在中空纤维(HF)孔上的氧化单壁碳纳米角(o-SWNHs)对三嗪类从水中直接浸入固相微萃取的潜力。为了获得在甲醇中的均匀分散体,装置的制造需要通过微波辐射氧化纳米颗粒。然后,在超声搅拌下将多孔中空纤维浸入到o-SWNH的甲醇分散体中。该程序允许将o-SWNH固定在中空纤维的孔中。为了进行萃取,将不锈钢丝引入纤维内部,以使o-SWNHs-HF垂直浸入水标准液/水样品中。将三嗪预浓缩在固定的o-SWNHs上,并进一步用150μL甲醇洗脱。蒸发溶剂,将残留物重新溶于10μL甲醇中,以提高灵敏度。选择气相色谱-质谱法作为仪器技术。检出限在0.05和0.1μgL〜(-1)之间,并且运行之间(低于10.2%)和纤维之间(低于12.8%)具有极好的精度(表示为相对标准偏差)。最终,该方法用于强化水中三嗪的测定,平均回收率达到90%。

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