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用媒染蓝9螯合后对痕量铀进行吸附溶出伏安法测量。

Adsorptive stripping voltammetric measurements of trace levels of uranium following chelation with mordant blue 9.

作者信息

Wang J, Zadeii J M

机构信息

Department of Chemistry, New Mexico State University, Las Cruces, NM 88003, USA.

出版信息

Talanta. 1987 Feb;34(2):247-51. doi: 10.1016/0039-9140(87)80207-2.

Abstract

The chelate of uranium with the azo dye Mordant Blue 9 is shown to be adsorbed and then reduced on the hanging mercury drop electrode. These properties have been exploited in developing a highly sensitive stripping voltammetric procedure for trace determination of uranium. With controlled adsorptive accumulation for 5 min, a detection limit near 2 x 10(-10)M uranium is obtained. Cyclic voltammetry has been used to characterize the interfacial and redox behaviour. The effect of various operational parameters on the stripping response is discussed. Experimental conditions include use of 1 x 10(-6)M Mordant Blue 9 in 0.05M acetate buffer (pH 6.5), an accumulation potential of -0.43 V, and a linear potential scan. The response is linear up to 1.2 x 10(-7)M uranium, and the relative standard deviation at 4.2 x 10(-8)M is 3.2%. The effects of possible interferences from organic surfactants or metal ions have been investigated.

摘要

已表明铀与偶氮染料媒染蓝9的螯合物会被悬汞滴电极吸附,然后在该电极上被还原。这些特性已被用于开发一种用于痕量测定铀的高灵敏度溶出伏安法。通过控制吸附富集5分钟,可获得接近2×10⁻¹⁰M铀的检测限。循环伏安法已用于表征界面和氧化还原行为。讨论了各种操作参数对溶出响应的影响。实验条件包括在0.05M醋酸盐缓冲液(pH 6.5)中使用1×10⁻⁶M媒染蓝9、-0.43 V的富集电位以及线性电位扫描。铀浓度高达1.2×10⁻⁷M时响应呈线性,4.2×10⁻⁸M时的相对标准偏差为3.2%。已研究了有机表面活性剂或金属离子可能产生的干扰影响。

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