Loofah-derived activated carbon supported on nickel foam (AC/Ni) electrodes for the electro-sorption of ammonium ion from aqueous solutions

被引:30
作者
Shih, Yu-Jen [1 ]
Dong, Cheng-Di [2 ]
Huang, Yao-Hui [3 ]
Huang, C. P. [4 ]
机构
[1] Natl Sun Yat Sen Univ, Inst Environm Engn, Kaohsiung 804, Taiwan
[2] Natl Kaohsiung Univ Sci & Technol, Dept Marine Environm Engn, Kaohsiung 811, Taiwan
[3] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 701, Taiwan
[4] Univ Delaware, Dept Civil & Environm Engn, Newark, DE 19716 USA
关键词
loofah sponge; Specific capacitance; Activated carbons; Electrosorption; Ammonium; CAPACITIVE DEIONIZATION; DOUBLE-LAYER; GRAPHITE-ELECTRODES; POROUS CARBON; ORGANIC-ACIDS; WASTE-WATER; FUEL-CELLS; REMOVAL; ADSORPTION; OXIDATION;
D O I
10.1016/j.chemosphere.2019.125259
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Activated carbon (AC), prepared from dried loofah sponge, was supported on nickel foam to fabricate AC/Ni electrodes. The characteristics of ammonium electrosorption on AC/Ni electrodes was studied. Results showed that AC prepared in one-step activation (without pre-pyrolysis), i.e., OAC, had relatively low crystallinity, high mesoporosity, and high specific capacitance compared to those made in two-step carbonation followed by activation. Adsorption and desorption density of NH4+ were measured at constant potential of -1.0 V (vs. Hg/HgO) and +0.1 V (vs. Hg/HgO), respectively. Non-faradaic charging contributed to the electrochemical storage and adsorption of ammonium ions on the AC surface with a maximal charge efficiency of 80%, at an applied potential of -1.0 V (vs. Hg/HgO). Multiple-layer adsorption isotherm better described the electrosorption of ammonium ion on OAC/Ni electrodes yielding a maximum adsorption capacity of 6 mg-N g(-1), which was comparable with other similar systems. Overall, results clearly demonstrated the effect of synthesis strategy on the capacitive charging behaviors of AC/Ni electrodes and its relationship to NH4+ electrosorption. (C) 2019 Elsevier Ltd. All rights reserved.
引用
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页数:10
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