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采用新型特异性膦改性聚合物微球预富集和高效液相色谱-电感耦合等离子体质谱法测定环境水体中的砷形态

Arsenic speciation in environmental waters by a new specific phosphine modified polymer microsphere preconcentration and HPLC-ICP-MS determination.

作者信息

Jia Xiaoyu, Gong Dirong, Wang Jiani, Huang Fuyi, Duan Taicheng, Zhang Xian

机构信息

Key Lab of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, PR China; Ningbo Key Laboratory of Urban Environmental Processes and Pollution Control, Ningbo Urban Environment Observation and Research Station, Chinese Academy of Sciences, Ningbo, 315830, PR China.

Department of Polymer Science and Engineering, Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo, 315211, PR China.

出版信息

Talanta. 2016 Nov 1;160:437-443. doi: 10.1016/j.talanta.2016.07.050. Epub 2016 Jul 25.

Abstract

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 25mL sample solution were 28, while for MMA and As(V) reached 30. The low detection limits of 1.2ngL(-1), 0.96ngL(-1), 0.82ngL(-1) and 0.91ngL(-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.

摘要

设计了一种新型的特定膦改性聚合物微球(PPMs),并将其用作核心吸附剂,通过在线固相萃取(SPE)全面富集环境水体中的无机和有机砷物种。避免使用任何氧化还原试剂,所有四种砷物种都被定量保留在具有大量带正电荷吸附基团的自制微型柱上,然后用硝酸铵和磷酸二氢铵的混合溶液快速洗脱(在数秒内)。通过高效液相色谱与电感耦合等离子体质谱联用(HPLC-ICP-MS)技术同时实现了As(III)、二甲基砷(DMA)、一甲基砷(MMA)和As(V)物种的痕量分离和测定。这项工作开发了一种通用的三正丁基膦功能化聚合物微球,用于高效可靠地在线同时预富集和检测无机和有机砷形态。在优化的实验条件下,用25mL样品溶液对As(III)和DMA的富集因子为28,而对MMA和As(V)则达到30。As(III)、DMA、MMA和As(V)的检测限分别低至1.2ngL⁻¹、0.96ngL⁻¹、0.82ngL⁻¹和0.91ngL⁻¹,相对标准偏差(RSD)分别为3.9%、5.6%、3.2%和4.5%。通过分析有证标准物质GSBZ 07-3171-2014对所开发的方法进行了验证,该方法有望用于湖水、河水和海水样品中砷物种的常规监测。

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