Preparation of high surface area-activated carbon from lignin of papermaking black liquor by KOH activation for Ni(II) adsorption

被引:192
作者
Gao, Yuan [1 ]
Yue, Qinyan [1 ]
Gao, Baoyu [1 ]
Sun, Yuanyuan [1 ]
Wang, Wenyu [1 ]
Li, Qian [1 ]
Wang, Yan [1 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Shandong Prov Key Lab Water Pollut Control & Reso, Jinan 250100, Peoples R China
关键词
Black liquor lignin-activated carbon; High specific area; Nickle; Adsorption; HEAVY-METAL IONS; AQUEOUS-SOLUTIONS; CHEMICAL ACTIVATION; PEANUT HULL; REMOVAL; EQUILIBRIUM; KINETICS; MICROWAVE; MECHANISM; ADSORBENT;
D O I
10.1016/j.cej.2012.09.038
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Low-cost activated carbon with high surface area was prepared from lignin of papermaking black liquor (BL) by KOH activation with pre-carbonization method. The effects of lignin/KOH ratio, activation temperature and activation time on the BET surface area were investigated. In addition, the adsorption capacity of Ni(II) on BLAC was also studied. Through BET surface area, scanning electron microscopy, Fourier transformed infrared spectroscopy and thermo gravimetric analysis, the BL-activated carbon (BLAC) was discovered to have porous structure with a high surface area up to 2943 m(2)/g. The results showed that the lignin/KOH ratio was the main factor influencing the surface area and the maximum surface area activated carbon was obtained at lignin/KOH ratio of 3:1, the activation temperature of 750 degrees C and the activation time of 1 h. The sorption experiments indicated that the pseudo-second-order model was well fitted the kinetic data and the adsorption equilibrium data were better simulated by Langmuir model. The adsorption ability of Ni(II) increased with increasing pH, indicating the electrostatic attraction mechanism. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:345 / 353
页数:9
相关论文
共 33 条
[1]   Adsorptive removal of heavy metal ions from industrial effluents using activated carbon derived from waste coconut buttons [J].
Anirudhan, T. S. ;
Sreekumari, S. S. .
JOURNAL OF ENVIRONMENTAL SCIENCES, 2011, 23 (12) :1989-1998
[2]  
[Anonymous], 2212005 CJT
[3]   Activated carbons developed from a rapidly renewable biosource for removal of cadmium(II) and nickel(II) ions from dilute aqueous solutions [J].
Basso, MC ;
Cerrella, EG ;
Cukierman, AL .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (02) :180-189
[4]   Water vapour adsorption on lignin-based activated carbons [J].
Bedia, Jorge ;
Rodriguez-Mirasol, Jose ;
Cordero, Tomas .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2007, 82 (06) :548-557
[5]   Adsorptive removal of copper(II) from aqueous solutions on activated carbon prepared from Tunisian date stones: Equilibrium, kinetics and thermodynamics [J].
Bouhamed, F. ;
Elouear, Z. ;
Bouzid, J. .
JOURNAL OF THE TAIWAN INSTITUTE OF CHEMICAL ENGINEERS, 2012, 43 (05) :741-749
[6]   Adsorbent ability of lignin-based activated carbons for the removal of p-nitrophenol from aqueous solutions [J].
Cotoruelo, Luis M. ;
Marques, Maria D. ;
Diaz, Francisco J. ;
Rodriguez-Mirasol, Jose ;
Rodriguez, Juan J. ;
Cordero, Tomas .
CHEMICAL ENGINEERING JOURNAL, 2012, 184 :176-183
[7]   Removal of Ni(II) from aqueous solution by adsorption onto hazelnut shell activated carbon:: equilibrium studies [J].
Demirbas, E ;
Kobya, M ;
Öncel, S ;
Sencan, S .
BIORESOURCE TECHNOLOGY, 2002, 84 (03) :291-293
[8]   Thermal stability and pyrolysis kinetics of organosolv lignins obtained from Eucalyptus globulus [J].
Dominguez, J. C. ;
Oliet, M. ;
Alonso, M. V. ;
Gilarranz, M. A. ;
Rodriguez, F. .
INDUSTRIAL CROPS AND PRODUCTS, 2008, 27 (02) :150-156
[9]   A comparison study of peach stone and acrylonitrile-divinylbenzene copolymer based activated carbons as chromium(VI) sorbents [J].
Duranoglu, Dilek ;
Trochimczuk, Andrzej W. ;
Beker, Ulker .
CHEMICAL ENGINEERING JOURNAL, 2010, 165 (01) :56-63
[10]   Methodical study of the chemical activation of Kraft lignin with KOH and NaOH [J].
Fierro, V. ;
Torne-Fernandez, V. ;
Celzard, A. .
MICROPOROUS AND MESOPOROUS MATERIALS, 2007, 101 (03) :419-431