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a rapid colorimetric method for measuring arsenic
Analytica Chimica Acta 526 (2004) 203–209
A rapid colorimetric method for measuring arsenic
concentrations in groundwater
R.K. Dhara,b,c,∗, Y. Zhenga,b,c , J. Rubenstonec , A. van Geenc
a School of Earth and Environmental Sciences, NSB D-216, Queens College, City University of Ne wYork,
65-30 Kissena Building, Flushing, NY 11367, USA
b Graduate School and University Center, City University of Ne wYork, NY, USA
c Lamont-Doherty Earth Observatory of Columbia University, Palisades, NY 10964, USA
Received 5 May 2004; received in revised form 16 September 2004; accepted 16 September 2004
Abstract
The arsenic content of groundwater consumed by millions of people in the developing world has become a major health concern. We
report here an optimization of the colorimetric method of Johnson and Pilson (1972) to accurately measure As concentrations in the
0.03–5.3 mol L−1 (2–400 g L−1) range in groundwater containing 2–30 mol L−1 dissolved phosphate. The optimization includes in-
creases in the concentrations of potassium iodate, ascorbic acid, antimonyl tartrate used for sample pre-treatment and color development that
significantly lowered the detection limit and shortened the reaction time. Mean recovery obtained for a suite of groundwater samples from
Bangladesh spiked with As in the 0.13–13 mol L−1 (10–1000 g L−1) range, the linear range of the method, was 97 ± 5% (n = 10). The
colorimetric method agrees within 5 g L−1 for As concentrations up to 0.67 mol L−1 (50 g L−1) and within 4% in the 0.67–5.3 mol L−1
(50–400 g L−1) range with As analysis of the same Bangladesh groundwater samples
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