On-site determination of arsenic in soil extract by anodic stripping voltammetry with gold film electrode after solid phase pretreatment

被引:2
作者
Furusho, Yoshiaki [1 ]
Makita, Nobuaki [1 ]
Ono, Masato [1 ]
Ishiyama, Takashi [2 ]
Takahashi, Motoyuki [2 ]
Motomizu, Shoji [3 ]
机构
[1] GL Sci Inc, Shinjuku Ku, Tokyo 1631130, Japan
[2] Ctr Environm Sci Saitama, Kisai, Saitama 3470115, Japan
[3] Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan
关键词
solid phase extraction; anodic stripping voltammetry; soil extract; arsenic;
D O I
10.2116/bunsekikagaku.56.1165
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method for the on-site estimation of arsenic (As) contamination in soil by solid-phase extraction with a resin based on molecular recognition technology (SPE-MRT) and anodic stripping voltammetry (ASV) using a gold film microelectrode was developed. Optimized pretreatments were carried out as follows: I g of soil sample was taken and put into polypropylene test tube containing 33 mL 1 M hydrochloric acid solution, which was heated at 70 degree Celsius for 5 min using graphite block hot plate. As in the sample was extracted by shaking for I min using an automatic mini-shaker system. The extract was finally filtered through a 0.45 mu m disk PTFE membrane filter. The extracted arsenic was electrodeposited on the gold film carbon microelectrode at -400 mV vs. Ag/AgCl for 1 min and the deposits were stripped at a rate of 5 mV/s to 580 mV vs. Ag/AgCl by using AnaLigo (R) TE-3, Cu in soil extract was removed with 1 M hydrochloric acid for the determination of As. The method can eliminate Cu interference. The detection limit was 0.5 mu g/L in soil extract. The results of voltammograms for As in the extracts from real soil samples were the same level as these obtained by a cross-check method using inductively coupled plasma mass spectroscopy (ICP-MS).
引用
收藏
页码:1165 / 1169
页数:5
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