Determination of inorganic and organic anionic arsenic species in water by ion chromatography coupled to hydride generation-inductively coupled plasma atomic emission spectrometry

被引:53
作者
Gettar, RT [1 ]
Garavaglia, RN [1 ]
Gautier, EA [1 ]
Batistoni, DA [1 ]
机构
[1] Comis Nacl Energia Atom, Gerencia Ctr Atom Constituyentes, Unidad Actividad Quim, RA-1429 Buenos Aires, DF, Argentina
关键词
water analysis; environmental analysis; detection; LC; inorganic cations; inorganic anions; organoarsenical compounds; arsenic;
D O I
10.1016/S0021-9673(00)00279-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of an analytical methodology for the specific determination of arsenite, arsenate and the organic species monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA), is described. The method is based on an ion chromatographic separation, coupled on-line to post-column generation of the gaseous hydrides by reaction with sodium tetrahydroborate in acidic medium. Detection and measurement were performed by inductively coupled plasma spectrometry operated in the atomic emission mode. Arsenic emission was monitored at 193.7 nm. Different types and sizes of anion-exchange columns, silica and polymeric, were tested using EDTA as eluent. Composition, acidity and flow-rate of the mobile phase were optimized in order to obtain the required resolution. Complete elution and resolution of the four species was achieved in about 6 min. Linear calibration curves were obtained in the 0.05-2 mu g ml(-1) range for As(III), As(V) and MMA, and between 0.1 and 2.0 mu g ml(-1) for DMA. The absolute limits of detection for 200-mu l sample injections were in the ng range, with DMA the compound measured with less sensitivity. Results of the analyses of natural samples, such as river and ground waters spiked with the studied species, suggested that analyte recoveries might be dependent on the sample composition. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:211 / 221
页数:11
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