1. Systematic study on the reduction efficiency of ascorbic acid and thiourea on selenate and selenite at high and trace concentrations.
- Author
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Zhang G, Gomez MA, Yao S, Ma X, Li S, Cao X, Zang S, and Jia Y
- Subjects
- Ascorbic Acid analysis, Mining, Oxidation-Reduction, Selenic Acid analysis, Selenious Acid analysis, Selenium analysis, Selenium Compounds, Sulfur, Thiourea analysis, Ascorbic Acid chemistry, Models, Chemical, Selenic Acid chemistry, Selenious Acid chemistry, Thiourea chemistry
- Abstract
Selenate (Se(VI)) and selenite (Se(IV)) are common soluble wastewater pollutants in natural and anthropogenic systems. We evaluated the reduction efficiency and removal of low (0.02 and 2 mg/L) and high (20 and 200 mg/L) Se(IV)
(aq) and Se(VI)(aq) concentrations to elemental (Se0 ) via the use of ascorbic acid (AA), thiourea (TH), and a 50-50% mixture. The reduction efficiency of AA with Se(IV)(aq) to nano- and micro-crystalline Se0 was ≥ 95%, but ≤ 5% of Se(VI)(aq) was reduced to Se(IV)(aq) with no Se0 . Thiourea was able to reduce ≤ 75% of Se(IV)(aq) to bulk Se0 at lower concentrations but was more effective (≥ 90%) at higher concentrations. Reduction of Se(VI)(aq) →Se (IV)(aq) with TH was ≤ 75% at trace concentrations which steadily declined as the concentrations increased, and the products formed were elemental sulfur (S0 ) and Sn Se8-n phases. The reduction efficiency of Se(IV)(aq) to bulk Se0 upon the addition of AA+TH was ≤ 81% at low concentrations and ≥ 90% at higher concentrations. An inverse relation to what was observed with Se(IV)(aq) was found upon the addition of AA+TH with Se(VI)(aq) . At low Se(VI)(aq) concentrations, AA+TH was able to reduce more effectively (≤ 61%) Se(VI)(aq) →Se(IV)(aq) →Se0 , while at higher concentrations, it was ineffective (≤ 11%) and Se0 , S0 , and Sn Se8-n formed. This work helps to guide the removal, reduction effectiveness, and products formed from AA, TH, and a 50-50% mixture on Se(IV)(aq) and Se(VI)(aq) to Se0 under acidic conditions and environmentally relevant concentrations possibly found in acidic natural waters, hydrometallurgical chloride processing operations, and acid mine drainage/acid rock drainage tailings. Graphical Abstract ᅟ.- Published
- 2019
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