Design and development of an automated flow injection instrument for the determination of arsenic species in natural waters

被引:7
作者
Hanrahan, Grady [1 ]
Fan, Tina K. [2 ]
Kantor, Melanie [3 ]
Clark, Keith [4 ]
Cardenas, Steven [4 ]
Guillaume, Darrell W. [5 ]
Khachikian, Crist S. [6 ]
机构
[1] Calif Lutheran Univ, Dept Chem, Thousand Oaks, CA 91360 USA
[2] Univ Calif Berkeley, Dept Civil & Environm Engn, Berkeley, CA 94720 USA
[3] Stanford Univ, Sch Humanities & Sci, Stanford, CA 94305 USA
[4] Calif State Univ Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90032 USA
[5] Calif State Univ Los Angeles, Dept Mech Engn, Los Angeles, CA 90032 USA
[6] Calif State Univ Los Angeles, Dept Civil Engn, Los Angeles, CA 90032 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ENVIRONMENTAL WATER; SPECIATION ANALYSIS; COLORIMETRIC METHOD; AQUEOUS SAMPLES; RAPID OXIDATION; POTABLE WATER; BLUE METHOD; FIELD; REDUCTION; MOBILITY;
D O I
10.1063/1.3202083
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The design and development of an automated flow injection instrument for the determination of arsenite [As(III)] and arsenate [As(V)] in natural waters is described. The instrument incorporates solenoid activated self-priming micropumps and electronic switching valves for controlling the fluidics of the system and a miniature charge-coupled device spectrometer operating in a graphical programming environment. The limits of detection were found to be 0.79 and 0.98 mu M for As(III) and As(V), respectively, with linear range of 1-50 mu M. Spiked ultrapure water samples were analyzed and recoveries were found to be 97%-101% for As(III) and 95%-99% for As(V), respectively. Future directions in terms of automation, optimization, and field deployment are discussed. (C) 2009 American Institute of Physics. [doi:10.1063/1.3202083]
引用
收藏
页数:5
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