کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
610619 880654 2009 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Prediction of iodide adsorption on oxides by surface complexation modeling with spectroscopic confirmation
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Prediction of iodide adsorption on oxides by surface complexation modeling with spectroscopic confirmation
چکیده انگلیسی

A deficiency in environmental iodine can cause a number of health problems. Understanding how iodine is sequestered by materials is helpful for evaluating and developing methods for minimizing human health effects related to iodine. In addition, 129I is considered to be strategically important for safety assessment of underground radioactive waste disposal. To assess the long-term stability of disposed radioactive waste, an understanding of 129I adsorption on geologic materials is essential. Therefore, the adsorption of I− on naturally occurring oxides is of environmental concern. The surface charges of hydrous ferric oxide (HFO) in NaI electrolyte solutions were measured by potentiometric acid–base titration. The surface charge data were analyzed by means of an extended triple-layer model (ETLM) for surface complexation modeling to obtain the I− adsorption reaction and its equilibrium constant. The adsorption of I− was determined to be an outer-sphere process from ETLM analysis, which was consistent with independent X-ray absorption near-edge structure (XANES) observation of I− adsorbed on HFO. The adsorption equilibrium constants for I− on β-TiO2 and γ-Al2O3 were also evaluated by analyzing the surface charge data of these oxides in NaI solution as reported in the literature. Comparison of these adsorption equilibrium constants for HFO, β-TiO2, and γ-Al2O3 based on site-occupancy standard states permitted prediction of I− adsorption equilibrium constants for all oxides by means of the Born solvation theory. The batch adsorption data for I− on HFO and amorphous aluminum oxide were reasonably reproduced by ETLM with the predicted equilibrium constants, confirming the validity of the present approach. Using the predicted adsorption equilibrium constants, we calculated distribution coefficient (KdKd) values for I− adsorption on common soil minerals as a function of pH and ionic strength.

The adsorption of I− was determined to be an outer-sphere process from ETLM analysis, which was consistent with independent XANES observation of I− adsorbed on HFO.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Colloid and Interface Science - Volume 332, Issue 2, 15 April 2009, Pages 309–316
نویسندگان
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