首页> 外文期刊>International journal of environmental analytical chemistry >Overestimation of geogenic arsenic in landfill leachate: interference of humic and phosphinic acid in a commercial test kit
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Overestimation of geogenic arsenic in landfill leachate: interference of humic and phosphinic acid in a commercial test kit

机译:高估垃圾填埋场渗滤液中的地源砷:商业测试套件中的腐殖酸和次膦酸的干扰

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Large-scale groundwater contamination by arsenic (As) requires economical yet reliable analytical procedures to monitor the quality of well water and the effluent of As elimination processes. The silver diethyldithiocarbamate (AgDDTC) method provides the basis of a series of colourimetric tests used as a compromise between semi-quantitative field-test kits and expensive instrumental analytics. This study aimed at understanding the significant As overestimation by the AgDDTC method observed in landfill leachate samples. Results of the AgDDTC test were up to threefold the levels obtained by reference analyses. Overestimation broadly agreed with the time course of chemical oxygen demand and total phosphorus in the leachate. We hypothesised that the interference was caused by reduced P species or humic acid (HA), respectively. To test this, As-AgDDTC determinations from As standards were conducted with phosphonic (H3PO3) and phosphinic acid (H3PO2) as well as two commercial HA as matrix components. While H3PO3 showed no effect, H3PO2 in concentrations of 0.06 to 28mgPL(-1) yielded As recoveries of up to 130%. This was probably due to the evolution of phosphine (PH3) as suggested by the absorption spectra recorded after reacting pure PH3 with AgDDTC in pyridine. The HA in concentrations of 0.6-320mg dissolved organic carbon L-1 gave As recoveries of up to 600%, possibly due to a chromophoric reaction of volatile HA digestion products formed during the reduction step. Significant As overestimation in the presence of the above-named compounds may require pre-oxidation of the samples. To recognise interference effects, the acquisition of full absorbance spectra may be recommendable in lieu of fixed wavelength analyses.
机译:砷(As)引起的大规模地下水污染需要经济而可靠的分析程序来监控井水的质量和As消除工艺的废水。二乙基二硫代氨基甲酸银(AgDDTC)方法提供了一系列比色测试的基础,这些比色测试是半定量现场测试套件与昂贵的仪器分析之间的折衷方案。这项研究旨在了解在垃圾渗滤液样本中观察到的通过AgDDTC方法得出的显着的As高估。 AgDDTC测试的结果是参考分析获得的水平的三倍。高估大致上与渗滤液中化学需氧量和总磷的时间变化一致。我们假设干扰分别是由减少的P物种或腐殖酸(HA)引起的。为了测试这一点,使用膦酸(H3PO3)和次膦酸(H3PO2)以及两种市售HA作为基质组分,从As标准品中进行As-AgDDTC测定。虽然H3PO3没有作用,但是H3PO2的浓度为0.06至28mgPL(-1)时,As的回收率高达130%。这是由于纯净的PH3与AgDDTC在吡啶中反应后记录的吸收光谱表明,膦(PH3)的演化。浓度为0.6-320mg的溶解有机碳L-1中的HA回收的砷高达600%,这可能是由于还原步骤中形成的挥发性HA消化产物发生了发色反应。重要的是,在上述化合物存在下的高估可能需要样品的预氧化。为了识别干扰效应,建议使用全吸收光谱来代替固定波长分析。

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