Modification of a continuous flow method for analysis of trace amounts of nitrate in iron-rich sediment pore-waters of mine pit lakes

被引:17
作者
Herzsprung, P
Duffek, A
Friese, K
de Rechter, M
Schultze, M
Von Tumpling, W
机构
[1] UFZ Helmholtz Ctr Environm Res, Ctr Environm Res Leipzig Halle, Dept Inland Water Res, D-39114 Magdeburg, Germany
[2] SKALAR Analyt GmbH, D-41812 Erkelenz, Germany
关键词
continuous flow analysis; nitrate; iron; mine pits; pore-water;
D O I
10.1016/j.watres.2005.02.017
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
Nitrate was analysed in pore-waters with high ionic strength. Extremely high concentrations of dissolved ferrous iron interfere common analytical methods. The automatic photometrical procedure based on the cadmium reduction method is often used for analysis of nitrate in water samples (continuous flow analysis CFA). An integrated dialysis usually serves for sample dilution and (or) sample purification (from particles). Iron was precipitated as iron hydroxide due to the imidazole buffer system (pH 7.5). The dialysis membrane is an effective barrier for iron hydroxide particles to prevent interferences within the cadmium column or the flow-cell. However, dialysis membrane is blocked successively after analysis of several iron-rich pore-water samples by agglomeration of precipitated iron. The blocking of nitrate diffusion through the dialysis membrane is tantamount to a decrease of analytical sensitivity to recognise by decreasing photometrical extinction. Minimising the iron deposition within the dialyser solved the problem. A simple modification of the CFA apparatus was found to keep the analytical sensitivity nearly constant: The mixing coil for the imidazole buffer was considerably elongated. Nearly all iron hydroxide was deposited at the glass coil surface installed before the dialyser. At least SO iron-rich samples could be analysed within one sample queue with a loss of sensitivity < 10%. The recovery of nitrate was about 95%, demonstrated by spiking experiments. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1887 / 1895
页数:9
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