کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1338441 1500284 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Studies of aqueous U(VI)–thiosalicylate complex formation via UV–Vis absorption spectrophotometry, TRLFS and potentiometry
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Studies of aqueous U(VI)–thiosalicylate complex formation via UV–Vis absorption spectrophotometry, TRLFS and potentiometry
چکیده انگلیسی

The formation of U(VI)–thiosalicylate (TSal) complexes in aqueous solutions (I = 0.1 M) was investigated over a wide range of pH values (from 3 to 9) using UV–Vis absorption and time-resolved luminescence spectroscopy, as well as by a potentiometric technique. It is demonstrated that the formation of U(VI)–TSal complexes, including monodentate, bidentate and ternary complexes, is responsible for the enhanced solubility of U(VI) and the strong U(VI)-luminescence quenching effects by TSal. In this study the stability constants of the complexes as well as two pKa values of TSal (pKa1 = 3.76 ± 0.05; pKa2 = 8.33 ± 0.07) are provided. The spectrophotometric analysis confirms the presence of both 1:1 and 1:2 (U(VI):TSal) charge-transfer complexes (log β101 = 7.59 ± 0.04 and log β102 = 13.67 ± 0.09). In luminescence quenching studies, mixed (dynamic and static) quenching processes are observed. The dynamic quenching for UO22+ is attributed to bimolecular excited-state processes by both the acidic and monobasic forms of TSal, i.e., H2TSal and HTSal−. The static quenching processes are explained by the formation of non-radiative ground-state complexes: UO2(HTSal)+ (log β111 = 12.11 ± 0.09) at pH 3.0; UO2(OH)(TSal)− and UO2(OH)2(TSal)2− (log β1–11 = 3.9 ± 0.1 and logβ 1–21 = −3.8 ± 0.1, respectively) at a higher pH. In particular, the formation of the latter ternary species is found to be responsible for the strong static quenching of hydroxo-uranyl species, i.e. (UO2)2(OH)22+ and (UO2)3(OH)5+.

Monodentate, bidentate and ternary uranium(VI)–thiosalicylate(TSal) complexes are identified. The uranium solubility increases in the presence of TSal. The charge-transfer band absorption by UO2(TSal)0 and UO2(TSal)22− is analyzed using UV–Vis spectrophotometry. The U(VI)-luminescence quenching effects are analyzed using TRLFS. The static quenching processes are also induced by UO2(HTSal)+, UO2(OH)(TSal)− and UO2(OH)2(TSal)2−.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Polyhedron - Volume 55, 17 May 2013, Pages 201–208
نویسندگان
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