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首页> 外文期刊>Analytical Letters >Determination of ultra trace amounts of uranium (VI) by adsorptive stripping voltammetry using L-3-(3, 4-dihydroxy phenyl) alanine as a selective complexing agent
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Determination of ultra trace amounts of uranium (VI) by adsorptive stripping voltammetry using L-3-(3, 4-dihydroxy phenyl) alanine as a selective complexing agent

机译:使用L-3-(3,4-二羟基苯基)丙氨酸作为选择性络合剂的吸附溶出伏安法测定超痕量铀(VI)

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摘要

The spectrophotometric behavior of uranium (VI) with L-3-(3, 4-dihydroxy phenyl) alanine (LDOPA) reagent revealed that the uranium can form a ML2 complex with LDOPA in solution. Thus a highly sensitive adsorptive stripping voltammetric protocol for measuring of trace uranium, in which the preconcentration was achieved by adsorption of the uranium-LDOPA complex at hanging mercury drop electrode (HMDE), is described. Optimal conditions were found to be a 0.02 M ammonium buffer (pH 9.5) containing 2.0 x 10(-5) M (LDOPA), an accumulation potential of -0.1V (versus Ag/AgCl) and an accumulation time of 120sec. The peak current and concentration of uranium accorded with linear relationship in the range of 0.5-300 ng ml(-1). The relative standard deviation (at 10 ng ml(-1)) is 3.6% and the detection limit is 0.27 ng ml(-1). The interference of some common ions was studied. Applicability to different real samples is illustrated. The attractive behavior of this reagent holds great promise for routine environmental and industrial monitoring of uranium.
机译:铀(VI)与L-3-(3,4-二羟基苯基)丙氨酸(LDOPA)试剂的分光光度行为表明,铀可以在溶液中与LDOPA形成ML2络合物。因此,描述了一种用于测量痕量铀的高灵敏吸附溶出伏安法,其中预浓缩是通过悬挂式汞滴电极(HMDE)吸附铀-LDOPA络合物而实现的。发现最佳条件是含有2.0 x 10(-5)M(LDOPA)的0.02 M铵缓冲液(pH 9.5),-0.1V的累积电位(相对于Ag / AgCl)和120秒的累积时间。铀的峰值电流和浓度在0.5-300 ng ml(-1)范围内符合线性关系。相对标准偏差(在10 ng ml(-1)时)为3.6%,检出限为0.27 ng ml(-1)。研究了一些常见离子的干扰。说明了对不同真实样品的适用性。该试剂的诱人性能为铀的常规环境和工业监测提供了广阔前景。

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