Sorption of Ni(II) by Fe(II) and EDTA-modified activated carbon derived from pyrophosphoric acid activation

被引:3
|
作者
Wang, Jing [1 ,2 ]
Wang, Yan [2 ,3 ]
Liu, Hai [2 ]
Zhang, Jian [2 ]
Zhang, Chenglu [2 ]
Wang, Jinhe [1 ]
机构
[1] Shandong Jianzhu Univ, Sch Municipal & Environm Engn, Jinan, Peoples R China
[2] Shandong Univ, Sch Environm Sci & Engn, Shandong Key Lab Water Pollut Control & Resource, Jinan 250100, Peoples R China
[3] Lanzhou Univ, Coll Earth & Environm Sci, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Activated carbon; Modification; Ni(II); Sorption; HEAVY-METAL IONS; AQUEOUS-SOLUTION; SURFACE-CHEMISTRY; LOTUS STALK; PHOSPHATE ACTIVATION; ADSORPTION BEHAVIOR; REMOVAL; NICKEL; COMPOSITE; WATER;
D O I
10.1080/19443994.2014.989917
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Activated carbon (LSAC) was obtained from lotus stalk by pyrophosphoric acid activation. The LSAC was modified by FeCl2 and Na(2)EDTA (Fe-EDTA/LSAC) to enhance its ability for Ni(II) sorption from aqueous solutions. The activated carbons were characterized by N-2 adsorption and desorption isotherms, Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction. The sorption of Ni(II) from aqueous solution onto the LSAC and Fe-EDTA/LSAC under various conditions of dosage, contact time, initial solution pH, initial Ni(II) concentration, and ionic strength was investigated to illustrate the mechanism and to quantify the sorption parameters. LSAC and Fe-EDTA/LSAC were mainly microporous with pores almost less than 4nm. Although the surface area of LSAC (824m(2)g(-1)) was much higher than that of Fe-EDTA/LSAC (445m(2)/g), the Ni(II) sorption capacity of Fe-EDTA/LSAC was larger than that of LSAC. The pH and ionic strength studies indicated that the main Ni(II) sorption mechanisms by the carbons were electrostatic attraction and cation exchange. The kinetics and equilibrium data agreed well with the pseudo-second-order kinetics model and Langmuir isotherm model.
引用
收藏
页码:3700 / 3707
页数:8
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