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Development of a method for speciation of inorganic arsenic in waters using solid phase extraction and electrothermal atomic absorption spectrometry

机译:固相萃取和电热原子吸收光谱法测定水中无机砷的方法

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A solid phase extraction (SPE) procedure based on Amberlite IRA 900 resin was developed for speciation and separation of inorganic arsenic species (III, V) and total As in water samples. The As species and total As in eluent solutions were determined by electrothermal atomic absorption spectrometry (ETAAS) using Ni chemical modifier with 1200 degrees C pyrolysis temperature. Experimental parameters such as pH value, sample volume, flow rate, volume and concentration of eluent solution for As(V) were optimised and 98.0 +/- 1.9% recovery was found at pH 4.0. Experimental adsorption capacity of the resin for As(V) was investigated and 229.9 mg g(-1) was found. Under optimised experimental conditions, instrumental parameters such as limit of detection (LOD) and limit of quantification (LOQ) found were 0.126 and 0.420 mu g L-1, respectively. Interference effects of coexisting ions in the sample matrix on the recovery of As(V) were investigated. Concentration of As(III) was obtained by subtracting As(V) concentration found at pH 4.0 from total As(III + V) found at pH 8.0. The accuracy of the method proposed by using the resin was tested for analysing As species in a waste water standard reference material (SRM, CWW-TM-D) and spiked real water samples with recovery above 95%. The method proposed was also applied to the determinations of As species and total As in underground hot waters and tap water with relative error below 3%.
机译:开发了一种基于Amberlite IRA 900树脂的固相萃取(SPE)程序,用于形态和分离水中样品中的无机砷物质(III,V)和总砷。通过电热原子吸收光谱法(ETAAS)使用Ni化学改性剂在1200℃的热解温度下确定洗脱液中的As种类和总As。优化了As(V)的pH值,样品量,流速,洗脱液体积和浓度等实验参数,在pH 4.0时回收率为98.0 +/- 1.9%。研究了该树脂对As(V)的实验吸附能力,发现229.9 mg g(-1)。在优化的实验条件下,仪器的检测限(LOD)和定量限(LOQ)分别为0.126和0.420μg L-1。研究了样品基质中共存离子对As(V)回收的干扰作用。从pH 8.0的总As(III + V)减去pH 4.0的As(V)浓度获得As(III)的浓度。测试了使用该树脂提出的方法的准确性,以分析废水标准参考材料(SRM,CWW-TM-D)和加标真实水中样品中的砷形态,回收率超过95%。该方法还用于测定地下热水和自来水中的砷形态和总砷,相对误差在3%以下。

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