CuO/g-C3N4 nanocomposite for elemental mercury capture at low temperature

被引:47
作者
Liu, Dongjing [1 ]
Lu, Cheng [2 ]
Wu, Jiang [2 ]
机构
[1] Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Peoples R China
[2] Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai 200090, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Graphitic carbon nitride; Elemental mercury; Copper oxide; Nanocomposite; Environmental remediation; CARBON NITRIDE NANOSHEETS; CATALYTIC-OXIDATION; IN-SITU; REMOVAL; REDUCTION; G-C3N4; CHARS; ADSORPTION; NO; PHOTOCATALYSIS;
D O I
10.1007/s11051-018-4374-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphitic carbon nitride (g-C3N4) with unique and versatile properties has gained increasing research concerns. Here, CuO/g-C3N4 nanocomposite is fabricated and employed for gas-phase mercury (Hg-0) removal at low temperature. Pure g-C3N4 performs well toward Hg-0 adsorption at 40-200 degrees C with the optimal Hg-0 removal efficiency of similar to 54.5% at 120 degrees C. CuO-modification can significantly promote the Hg-0 capture ability of g-C3N4, probably due to the intimate interface contact of CuO and g-C3N4. The Hg-0 removal efficiency of g-C3N4 first increases and then decreases with rising temperature, while temperature shows a promotional effect on Hg-0 removal efficiency of CuO/g-C3N4. Hg-0 is oxidized into HgO by the chemisorbed oxygen originated from the O-C-N structure of g-C3N4 and the lattice oxygen of CuO. g-C3N4 can be efficiently activated by modifying with CuO toward enhanced Hg-0 oxidation ability, presumably attributed to the electron transfer at the interface of CuO and g-C3N4.
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页数:11
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