酸性溶液中的铀酰荧光:四甲基铵(TMA+)的猝灭效应

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Thomas D. Persinger, Michael C. Heaven, Richard E. Wilson
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引用次数: 0

摘要

在低ph的水溶液中,研究了不同阳离子对铀酰发光的猝灭作用。在硝酸、硝酸和离子浓度恒定的条件下,研究了不同硝酸盐溶液中不同阳离子对铀酰发光的猝灭作用。研究了碱金属(Li+、Na+、Rb+)和季铵离子(NH4+)、(CH3)4N+ (TMA+)、(C2H5)4N+ (TEA+)。含有TMA+的溶液比其他阳离子更明显地降低了铀酰荧光的寿命。铀酰发射光谱也显示TMA+增加了铀酰与硝酸盐离子之间络合物的形成。在20℃下,大多数溶液的荧光衰减寿命在1.4 ~ 1.9 μs之间,而1.8 M TMA+使铀酰荧光衰减寿命降至0.6 μs。衰减率与浓度的关系(Stern-Volmer图)表明,Li+、TMA+和TEA+在较高阳离子浓度下的荧光衰减率增加是一个动态猝灭过程。研究了D2O中衰变速率和动力学的温度依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Uranyl fluorescence in acidic solution: quenching effects by tetramethylammonium (TMA+)

Uranyl fluorescence in acidic solution: quenching effects by tetramethylammonium (TMA+)
The quenching of uranyl luminescence by various cation species was studied in aqueous media at low pH. Solutions with different nitrate salts, held at constant uranyl nitrate, nitric acid, and ion concentration, were tested to examine the quenching effects of the cations from the nitrate salts. Alkali metal (Li+, Na+, Rb+) and quaternary ammonium cations (NH4+), (CH3)4N+ (TMA+), (C2H5)4N+ (TEA+) were investigated. Solutions containing TMA+ reduced the lifetime of uranyl fluorescence significantly more than the other cations. Uranyl emission spectra also showed that TMA+ increased the complex formation between uranyl and nitrate ions. Fluorescence decay lifetime measurements for most solutions yielded values between 1.4–1.9 μs at 20 °C, while 1.8 M TMA+ reduced the lifetime of uranyl fluorescence to 0.6 μs. Decay rate versus concentration data (Stern–Volmer plots) indicated a dynamic quenching process with increasing fluorescence decay rates at higher cation concentrations for Li+, TMA+, and TEA+. The temperature dependencies of the decay rates and the kinetics in D2O were also examined.
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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