Institut für Kernchemie, Fritz-Strassmann-Weg 2, Johannes Gutenberg-Universität, Mainz, Germany.
Electrophoresis. 2018 Dec;39(23):3013-3021. doi: 10.1002/elps.201800318. Epub 2018 Sep 17.
The rate constants k of the reduction of 5 × 10 M Np(V) to Np(IV) by hydroxylamine hydrochloride (HAHCl) in 1 M HCl have been determined by CE-ICP-MS in the temperature range of ϑ = 30-70°C and with varying concentrations of HAHCl from 1 to 7.2 M. The reaction was found to have (pseudo)first order kinetics with respect to HAHCl. The experimental results for k ranged from 0.0029(1) min (ϑ = 40°C, c(HAHCl) = 3 M) to 0.039(7) min (ϑ = 60°C, c(HAHCl) = 7.2 M). The activation energy of the reaction was determined as E = (72 ± 10) kJ/mol. These results and a comparison with literature data show that the coupling of CE to ICP-MS provides a powerful analytical tool for the investigation of the kinetic aspects of redox reactions of actinides at low concentrations. On the basis of this proof-of-principle study, the method presented here can be extended to the investigation of the kinetic parameters of other redox systems containing different actinides (or transition metals) and oxidants/reductants.
在 1 M HCl 中,通过 CE-ICP-MS 测定了 5×10^-5 M Np(V)与盐酸羟胺(HAHCl)还原为 Np(IV)的速率常数 k,温度范围为θ=30-70°C,HAHCl 的浓度从 1 到 7.2 M 不等。该反应对 HAHCl 表现出(准)一级动力学。k 的实验结果范围从 0.0029(1) min(θ=40°C,c(HAHCl) = 3 M)到 0.039(7) min(θ=60°C,c(HAHCl) = 7.2 M)。反应的活化能确定为 E = (72 ± 10) kJ/mol。这些结果以及与文献数据的比较表明,CE 与 ICP-MS 的结合为研究低浓度下锕系元素氧化还原反应的动力学方面提供了一种强大的分析工具。基于这一原理验证研究,本文提出的方法可以扩展到其他含有不同锕系元素(或过渡金属)和氧化剂/还原剂的氧化还原体系动力学参数的研究。