Simultaneous adsorption of Ni(II) and Mn(II) ions from aqueous solution unto a Nigerian kaolinite clay

被引:168
作者
Dawodu, Folasegun Anthony [1 ]
Akpomie, Kovo Godfrey [1 ,2 ]
机构
[1] Univ Ibadan, Dept Chem Ind, Ibadan, Nigeria
[2] Projects Res & Dev Inst PRODA, Mat & Energy Technol Dept, Enugu, Nigeria
来源
JOURNAL OF MATERIALS RESEARCH AND TECHNOLOGY-JMR&T | 2014年 / 3卷 / 02期
关键词
Adsorption; Ni(II); Mn(II); Kaolinite; Kinetics; Isotherms; HEAVY-METAL IONS; ACTIVATED CARBON; REMOVAL; EQUILIBRIUM; BIOSORPTION; KINETICS; LEAD; COPPER; CADMIUM; SORPTION;
D O I
10.1016/j.jmrt.2014.03.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An unmodified Nigerian kaolinite clay (UAK) was utilized as a low-cost adsorbent for the removal of Ni(II) and Mn(II) ions from a binary solution of both metal ions. Batch adsorption methodology was used to evaluate the effect of solution pH, initial metal ion concentration, sorbent dose, particle size, contact time, temperature and ligand on adsorption. FTIR, XRD and SEM analysis were used to characterize the adsorbent. The equilibrium isotherm data were analyzed using the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich (D-R) isotherm model. The Freundlich isotherm model provided the best fit to the experimental data for both metal ions as indicated by the values of the regression coefficient. The Langmuir monolayer maximum adsorption capacities for Ni(II) and Mn(II) ions are 166.67 mg/g and 111.11 mg/g, respectively. The kinetic data were analyzed using the pseudo-first order, pseudo-second order equations, the Elovich equation and intraparticle diffusion rate equation. The Elovich equation gave the best fit to the experimental data for both metal ions. The presence of intraparticle diffusion mechanism was indicated, although it was not the sole rate determining step. Thermodynamic studies indicated an endothermic, spontaneous and a physisorption process between both metal ions and UAK. The results showed that the kaolinite can be utilized as a low-cost adsorbent for the removal of Ni(II) and Mn(II) ions from solution. (C) 2014 Brazilian Metallurgical, Materials and Mining Association. Published by Elsevier Editora Ltda.
引用
收藏
页码:129 / 141
页数:13
相关论文
共 74 条
  • [51] Adsorption equilibrium modeling and solution chemistry dependence of fluoride removal from water by trivalent-cation-exchanged zeolite F-9
    Onyango, MS
    Kojima, Y
    Aoyi, O
    Bernardo, EC
    Matsuda, H
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2004, 279 (02) : 341 - 350
  • [52] Rhoades J. D., 1982, METHODS SOIL ANAL 2
  • [53] Removal of Lead(II) from Aqueous Solutions using Pre-boiled and Formaldehyde-Treated Onion Skins as a New Adsorbent
    Saka, Cafer
    Sahin, Omer
    Demir, Halil
    Kahyaoglu, Mustafa
    [J]. SEPARATION SCIENCE AND TECHNOLOGY, 2011, 46 (03) : 507 - 517
  • [54] Specific surface: determination and relevance
    Santamarina, JC
    Klein, KA
    Wang, YH
    Prencke, E
    [J]. CANADIAN GEOTECHNICAL JOURNAL, 2002, 39 (01) : 233 - 241
  • [55] Biosorption of Cd(II), Cr(III), and Cr(VI) by saltbush (Atriplex canescens) biomass:: Thermodynamic and isotherm studies
    Sawalha, Maather F.
    Peralta-Videa, Jose R.
    Romero-Gonzalez, Jaime
    Gardea-Torresdey, Jorge L.
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2006, 300 (01) : 100 - 104
  • [56] Slejko F.L., 1985, ADSORPTION TECHNOLOG
  • [57] Study of the selection mechanism of heavy metal (Pb2+, Cu2+, Ni2+, and Cd2+) adsorption on clinoptilolite
    Sprynskyy, Myroslav
    Buszewski, Boguslaw
    Terzyk, Artur P.
    Namiesnik, Jacek
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2006, 304 (01) : 21 - 28
  • [58] Adsorption of cadmium and copper by modified kaolinite
    Suraj, G
    Iyer, CSP
    Lalithambika, M
    [J]. APPLIED CLAY SCIENCE, 1998, 13 (04) : 293 - 306
  • [59] On the removal of Mn2+ ions by adsorption onto natural and activated Chilean zeolites
    Taffarel, Silvio Roberto
    Rubio, Jorge
    [J]. MINERALS ENGINEERING, 2009, 22 (04) : 336 - 343
  • [60] Tempkin M.J., 1940, ACTA PHYSICOCHIM R S, V12, P217, DOI DOI 10.1016/J.JHAZMAT.2008.12.093