Adsorption of Zn2+ and Cd2+ Ions on Vermiculite in Buffered and Unbuffered Aqueous Solutions

被引:9
作者
Wu, Xiaofu [1 ]
Zhou, Hailan [2 ]
Zhao, Fang [1 ]
Zhao, Chong [3 ]
机构
[1] Cent S Univ Forestry & Technol, Inst Environm Sci & Engn, Changsha 410004, Hunan, Peoples R China
[2] Hunan Acad Environm Protect, Changsha 410004, Hunan, Peoples R China
[3] Shandong Water Polytechn, Rizhao, Shandong, Peoples R China
关键词
METAL-IONS; GAMMA-AL2O3; SURFACE; ACTIVATED CARBON; DESORPTION; SORPTION; REMOVAL; BEHAVIOR; WATER; EQUILIBRIUM; BENTONITE;
D O I
10.1260/0263-6174.27.10.907
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Studies of Zn2+ and Cd2+ ion adsorption onto vermiculite from buffered and unbuffered aqueous solutions were conducted in order to compare their ion adsorption behaviours in different systems. The use of buffer reagents had a strong and negative effect on the adsorption of the metal ions under study. The experimental data obtained from both the buffered and unbuffered solutions could not be described by a single traditional adsorption isotherm due to the effect of the adsorbent concentration (W). The equilibrium ion concentration in bulk solution (Z) and the equilibrium ion adsorption density (X/W ratio) decreased with increasing W in both buffered and unbuffered systems, indicating that the use of a buffer solution is not an effective measure for eliminating the effect of the adsorbent concentration. The addition of competitive ions (H+, Cd2+ and Zn2+) greatly reduced the adsorption of the target metal ion. Within the pH range tested (initial pH < 7), the competitive effect of H+ ions was equivalent to that of Zn2+ and Cd2+ ions. In unitary, binary and ternary systems, highly significant linear correlations were obtained between the change in the ionic strength (Delta I) and the quantity of ion adsorption. The results obtained suggest that it is not necessary to control the ionic strength in ion adsorption experiments because Delta I is a function of ion adsorption, and the use of buffer reagents has a negative effect on ion adsorption.
引用
收藏
页码:907 / 919
页数:13
相关论文
共 37 条
[1]   Surface speciation modeling of heavy metals in kaolin: Implications for electrokinetic soil remediation processes [J].
Al-Hamdan, AZ ;
Reddy, KR .
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY, 2005, 11 (5-6) :529-546
[2]   Continuous cephalosporin C purification: dynamic modelling and parameter validation [J].
Barboza, M ;
Hokka, CO ;
Maugeri, F .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2002, 25 (03) :193-203
[3]   Chromium uptake from tricomponent solution in zeolite fixed bed [J].
Barros, M. A. S. D. ;
Zola, A. S. ;
Arroyo, P. A. ;
Tavares, C. R. G. ;
Sousa-Aguiar, E. F. .
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY, 2006, 12 (04) :239-248
[4]   Competitive binding of Cu2+ and Zn2+ to live cells of Shewanella putrefaciens [J].
Claessens, Jacqueline ;
Van Cappellen, Philippe .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (03) :909-914
[5]   Analysis of application of Langmuir isotherm to heterogeneous systems: High-pressure conditions [J].
Cordeiro, CN ;
da Rocha, MS ;
Faleiros, AC ;
Iha, K .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 286 (02) :459-461
[6]   The adsorption of phloretin to lipid monolayers and bilayers cannot be explained by Langmuir adsorption isotherms alone [J].
Cseh, R ;
Benz, R .
BIOPHYSICAL JOURNAL, 1998, 74 (03) :1399-1408
[7]   SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .2. SURFACE PROPERTIES OF AMORPHOUS IRON OXYHYDROXIDE AND ADSORPTION OF METAL-IONS [J].
DAVIS, JA ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 67 (01) :90-107
[8]  
de Vicente MES, 2004, J CHEM EDUC, V81, P750
[9]   A comparative study on determination of the equilibrium, kinetic and thermodynamic parameters of biosorption of copper(II) and lead(II) ions onto pretreated Aspergillus niger [J].
Dursun, AY .
BIOCHEMICAL ENGINEERING JOURNAL, 2006, 28 (02) :187-195
[10]   Removal of endosulfan and methoxychlor from water on carbon slurry [J].
Gupta, Vinod K. ;
Ali, Imran .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (03) :766-770