The oxidative decomposition of arsenopyrite is an important source of As in surface environment. This study investigated the oxidative dissolution of arsenopyrite by O and aqueous arsenic transformation at different pHs, dissolved oxygen (DO) contents, and temperatures in the absence and presence of EDTA. The oxidative dissolution was greatly inhibited at neutral and alkaline pH in the absence of EDTA. However, in the presence of EDTA, the oxidative dissolution rate increased linearly from pH 4 to 7. The highest dissolution rate was 3-4 times higher than that at pH 4 and 1-2 orders of magnitude higher than that at pH 7 in the absence of EDTA. This is possibly due to the lack of Fe oxyhydroxides on the surface of arsenopyrite. In the pH range of 7-10, the oxidative dissolution rate decreased linearly, possibly due to the formation of goethite and/or hematite coating. The oxidation of released arsenite (As) to arsenate (As) took place simultaneously during the oxidative dissolution of arsenopyrite in the presence of dissolved Fe without EDTA, while no obvious aqueous As oxidation was observed in the presence of EDTA, indicating that aqueous Fe species play an important role in As oxidation.
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http://dx.doi.org/10.1016/j.jhazmat.2017.12.038 | DOI Listing |
ACS Appl Mater Interfaces
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Key Laboratory of Low Carbon Energy and Chemical Engineering of Gansu Province, Lanzhou 730050, China.
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Department of Earth Sciences, Utrecht University, 3584 CB Utrecht, The Netherlands.
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View Article and Find Full Text PDFAdv Sci (Weinh)
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School of Materials Science and Engineering, Harbin Institute of Technology, Harbin, 150001, China.
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Department of Pharmaceutics, College of Pharmacy, University of Hail, Hail 81442, Saudi Arabia. Electronic address:
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View Article and Find Full Text PDFInt J Pharm
January 2025
Universidade de Coimbra, Faculdade de Farmácia, Coimbra 3000-148 Portugal; i3S, IBMC, Rua Alfredo Allen, Porto 4200-135, Portugal. Electronic address:
The pharmaceutical industry is striving to develop innovative and promising tools, increasingly embracing new data-driven approaches, to understand, improve and accelerate the drug product development process. While extended release (ER) oral formulations offer a number of advantages, including maintenance of therapeutic drug levels, a reduction in dosing frequency, and minimization of side effects, achieving consistent drug release profiles remains a significant challenge. As a critical attribute for drug absorption into systemic circulation, in vitro dissolution testing represents a time-consuming and complex method for the evaluation of such formulations.
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