4.7 Article

Arsenic removal in aqueous solutions using FeS2

期刊

JOURNAL OF ENVIRONMENTAL MANAGEMENT
卷 286, 期 -, 页码 -

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jenvman.2021.112246

关键词

Arsenic contamination; Low-cost adsorbents; Natural minerals; Persulfate; Pyrite

资金

  1. Doctoral Scientific Research Foundation of the Suzhou University [2019jb14]
  2. University students' innovation and entrepreneurship program of Anhui Province [201910379169]
  3. TWAS-UNESCO [3240314536]
  4. University students' innovation and entrepreneurship program of China [202010379015]

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The study demonstrated the technical feasibility of pyrite and/or persulfate oxidation system for effective arsenic removal from aqueous solutions. Persulfate addition promoted complete removal of arsenic at optimized conditions, meeting WHO's arsenic maximum contaminant limit. The redox mechanisms involved electron transfer from pyrite to Fe3+ for persulfate decomposition, oxidizing As(III) to As(V).
This study tested the technical feasibility of pyrite and/or persulfate oxidation system for arsenic (As) removal from aqueous solutions. The effects of persulfate on As removal by the pyrite in the integrated treatment were also investigated. Prior to the persulfate addition into the reaction system, the physico-chemical interactions between As and the pyrite alone in aqueous solutions were explored in batch studies. The adsorption mechanisms of As by the adsorbent were also presented. At the same As concentration of 5 mg/L, it was found that As(III) attained a longer equilibrium time (8 h) than As(V) (2 h), while the pyrite worked effectively at pH ranging from 6 to 11. At optimum conditions (0.25 g/L of pyrite, pH 8.0 and 5 mg/L of As(III) concentration), the addition of persulfate (0.5 mM) into the reaction promoted a complete removal of arsenic from the solutions. Consequently, this enabled the treated effluents to meet the arsenic maximum contaminant limit (MCL) of <10 ?g/L according to the World Health Organization (WHO)?s requirements. The redox mechanisms, which involved electron transfer from the S22- of the pyrite to Fe3+, supply Fe2+ for persulfate decomposition, oxidizing As(III) to As(V). The sulfur species played roles in the redox cycle of the Fe3+/Fe2+ of the pyrite by giving its electrons, while the As(III) oxidation to As(V) was attributed to the pyrite. Overall, this work reveals the applicability of the pyrite as an adsorbent for water treatment and the importance of persulfate addition to promote a complete As removal from aqueous solutions.

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