The enhanced effect of oxalic acid on the electroreduction of Cr(VI) via formation of intermediate Cr(VI)-oxalate complex
被引:11
作者:
Liu, Yijie
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CNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Shandong, Peoples R ChinaCNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
Liu, Yijie
[1
,2
]
Xin, Shuaishuai
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机构:
Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Shandong, Peoples R ChinaCNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
Xin, Shuaishuai
[2
]
Jiang, Bo
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CNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Shandong, Peoples R ChinaCNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
Jiang, Bo
[1
,2
]
机构:
[1] CNPC Res Inst Safety & Environm Technol, State Key Lab Petr Pollut Control, Beijing 102206, Peoples R China
[2] Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Shandong, Peoples R China
In this study, the enhanced effect of oxalic acid (Ox) on Cr(VI) electroreduction was evaluated. It was found that for Cr(VI)-contaminated solution ([Cr(VI)](0) = 1.0 mM, pH = 3.0), addition of 5.0 mM Ox can significantly increase Cr(VI) reduction from 0.36 to 1.0 mM within 90 min electrolysis reaction, accompanying with the increase of current efficiency from 19% to 53%. Increasing initial Ox concentration (0-10 mM) and electric current (10-40 mA) facilitated Cr(VI) reduction, whereas it was inhibited with decreasing solution pH value (2.0-3.5) and elevating Cr(VI) concentration (0.1-2.0 mM), respectively. Results show that reactive electron was the primary reductant for the heterogeneous reduction of Cr(VI) on the cathode. In addition, Ox can also serve as an electron donor for the homogeneous reduction of Cr(VI). During this process, the formation of Cr(VI)-oxalate complex is indispensable for the enhanced Cr(VI) reduction. The coordination of Ox with Cr(VI) did not only make the structure of Cr(VI) more distorted but also improved the reactivity of Cr(VI) in Cr(VI)-oxalate complex toward reduction reaction. In general, this study provides an energy-efficient and environmentally benign strategy for the treatment of Ox and Cr(VI) co-contaminated wastewater.