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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Arsenic speciation in environmental waters by a new specific phosphine modified polymer microsphere preconcentration and HPLC-ICP-MS determination
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Arsenic speciation in environmental waters by a new specific phosphine modified polymer microsphere preconcentration and HPLC-ICP-MS determination

机译:通过新的特定膦改性的聚合物微球预富集和HPLC-ICP-MS测定环境水中的砷形态

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A new specific phosphine modified polymer microsphere (PPMs) was designed and used as the core adsorbent to comprehensively enrich both inorganic and organic arsenic species in environmental waters by on line solid-phase extraction (SPE). Avoiding any redox reagent, all the four arsenic species have been quantitatively retained on the home made mini-column with large number of positively charged adsorption groups, and then eluted rapidly (within seconds) with a mixed solution of ammonium nitrate and ammonium dihydrogen phosphate. The trace separation and determination of As(III), DMA, MMA and As(V) species have been simultaneously achieved by high performance liquid chromatography hyphenated to inductively coupled plasma spectrometry (HPLC-ICP-MS) technique. This work has developed a versatile tri-n-butylphosphine functionalized polymer microsphere for an efficient and reliable on-line of simultaneous preconcentration and detection of inorganic and organic arsenic speciation. Under the optimized experimental conditions, the enrichment factors obtained for As(III) and DMA with 25 mL sample solution were 28, while for MMA and As(V) reached 30. The low detection limits of 1.2 ng L-1, 0.96 ng L-1, 0.82 ng L-1 and 0.91 ng L-1, with the relative standard deviations (RSDs) of 3.9%, 5.6%, 3.2% and 4.5% were obtained for As(III), DMA, MMA and As(V), respectively. The developed method was validated by analyzing Certified Reference Materials GSBZ 07-3171-2014, promising for routine monitoring of arsenic species in lake water, river water and seawater samples. (C) 2016 Elsevier B.V. All rights reserved.
机译:设计了一种新的特定的膦改性聚合物微球(PPM),并将其用作核心吸附剂,通过在线固相萃取(SPE)来全面富集环境水中的无机和有机砷物质。避免使用任何氧化还原试剂,所有四种砷物质均已定量保留在带有大量带正电荷的吸附基团的微型小柱中,然后用硝酸铵和磷酸二氢铵的混合溶液快速洗脱(数秒内)。痕量分离和测定As(III),DMA,MMA和As(V)种类已通过连接到电感耦合等离子体光谱法(HPLC-ICP-MS)的高效液相色谱同时实现。这项工作已经开发了一种通用的三正丁基膦官能化聚合物微球,可高效,可靠地在线同时进行无机和有机砷形态的预浓缩和检测。在优化的实验条件下,使用25 mL样品溶液获得的As(III)和DMA的富集因子为28,而MMA和As(V)的富集因子达到30。低检测限为1.2 ng L-1、0.96 ng L -1、0.82 ng L-1和0.91 ng L-1的As(III),DMA,MMA和As(V)的相对标准偏差(RSD)为3.9%,5.6%,3.2%和4.5% ), 分别。通过分析认证参考材料GSBZ 07-3171-2014对开发的方法进行了验证,有望用于常规监测湖水,河水和海水样品中的砷物种。 (C)2016 Elsevier B.V.保留所有权利。

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