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首页> 外文期刊>International journal of environmental analytical chemistry >Dispersive liquid-liquid microextraction and microsample injection system coupled with inductively coupled plasma-mass spectrometry for inorganic arsenic speciation in natural waters
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Dispersive liquid-liquid microextraction and microsample injection system coupled with inductively coupled plasma-mass spectrometry for inorganic arsenic speciation in natural waters

机译:分散液液微萃取和微量进样系统与电感耦合等离子体质谱联用,用于天然水中的无机砷形态

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摘要

A method was developed for inorganic arsenic speciation analysis of water samples by a microsample injection system coupled with inductively coupled plasma mass spectrometry (MIS-ICP-MS) following a validated dispersive liquid-liquid microextraction (DLLME). Prior to DLLME speciation analysis, a simple robust microsample injection system was successfully adapted to ICP-MS. A sampling volume of 90 μL provided almost the same signals as the signals obtained by means of a conventional continuous nebulization sampling system for the ICP-MS instrument. After DLLME, the final solution was injected into nebulizer of ICP-MS using the microsample injection system. Under the optimized conditions, the analyte from only 5.0 mL water sample was concentrated by a factor of 48 with detection limits reaching 0.0031 μL~(-1) for arsenic. The calibration curve had a linear range of 0.0084-0.0800μg L~(-1) (r~2 = 0.999). The relative standard deviations (RSD, n = 6) were <4%. The proposed method was applied to the speciation of inorganic arsenic in various water samples with satisfactory results. The determination of arsenite and total As in river, pond, tap and bottled water samples was acheived by the standard addition method. The recoveries for spiked As(Ⅲ) and As(Ⅴ) from understudied water samples were in the range of 95-108%.
机译:经过验证的液-液微萃取(DLLME),开发了一种通过微量样品注射系统与电感耦合等离子体质谱法(MIS-ICP-MS)进行水样中无机砷形态分析的方法。在进行DLLME形态分析之前,简单的耐用型微量样品进样系统已成功应用于ICP-MS。 90μL的采样量提供的信号几乎与通过ICP-MS仪器的常规连续雾化采样系统获得的信号相同。 DLLME之后,使用微量样品注射系统将最终溶液注射到ICP-MS雾化器中。在优化的条件下,仅将5.0 mL水样品中的分析物浓缩至48倍,砷的检出限达到0.0031μL〜(-1)。校正曲线的线性范围为0.0084-0.0800μgL〜(-1)(r〜2 = 0.999)。相对标准偏差(RSD,n = 6)<4%。该方法用于各种水样中无机砷的形态鉴定,结果令人满意。采用标准添加法测定河流,池塘,自来水和瓶装水样品中的砷和总砷。从被研究水样中加标的砷(Ⅲ)和砷(Ⅴ)的回收率在95%至108%之间。

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