Monitoring of trace amounts of lead on an adsorbent by X-ray absorption spectroscopy combined with a fluorescence spectrometer

被引:16
|
作者
Izumi, Y
Kiyotaki, F
Seida, Y
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Environm Chem & Engn, Midori Ku, Yokohama, Kanagawa 2268502, Japan
[2] Inst Res & Innovat, Kashiwa, Chiba 2770861, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2002年 / 106卷 / 07期
关键词
D O I
10.1021/jp015539d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A trace amount of lead on adsorbent Mg6Fe2(OH)(16)(CO3)(.)3H(2)O was selectively monitored by XAS combined with a fluorescence spectrometer. In the presence of dominant scattered and emitted X-rays derived from heavy elements (Fe and Mg), large quantities of heavy elements predominantly absorb the incident photons and the X-ray fluorescence derived from trace amounts of elements is very weak compared to scattered + emitted X-rays derived from heavy elements. Pb Lalpha(1) emission was counted during XAS measurements with a fluorescence spectrometer of energy resolution of 1.1 eV. The obtained spectrum was compared to the spectra for standard Pb2+ compounds. The ion exchange mechanism FeO(OH) + Pb2+ --> FeO-OPb+ + H+ was rejected, but a eutectic mixture of PbCO3 and Pb(OH)(2) may be coagulated on the basic surface of adsorbent.
引用
收藏
页码:1518 / 1520
页数:3
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