Carboxymethyl-β-cyclodextrin conjugated magnetic nanoparticles as nano-adsorbents for removal of copper ions: Synthesis and adsorption studies

被引:455
作者
Badruddoza, A. Z. M. [1 ]
Tay, A. S. H. [1 ]
Tan, P. Y. [1 ]
Hidajat, K. [1 ]
Uddin, M. S. [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
关键词
Magnetic nanoparticles; Carboxymethyl-beta-cyclodextrin; Copper adsorption; Isotherms; Kinetic model; AQUEOUS-SOLUTION; HEAVY-METALS; ORGANIC-COMPOUNDS; CARBON NANOTUBES; CHITOSAN; FE3O4; WATER; ACID; CU(II); LEAD;
D O I
10.1016/j.jhazmat.2010.10.029
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel nano-adsorbent, carboxymethyl-beta-cyclodextrin modified Fe(3)O(4) nanoparticles (CMCD-MNPs) is fabricated for removal of copper ions from aqueous solution by grafting CM-beta-CD onto the magnetite surface via carbodiimide method. The characteristics results of FTIR, TEM, TGA and XPS show that CM-beta-CD is grafted onto Fe(3)O(4) nanoparticles. The grafted CM-beta-CD on the Fe(3)O(4) nanoparticles contributes to an enhancement of the adsorption capacity because of the strong abilities of the multiple hydroxyl and carboxyl groups in CM-beta-CD to adsorb metal ions. The adsorption of Cu(2+) onto CMCD-MNPs is found to be dependent on pH and temperature. Adsorption equilibrium is achieved in 30 min and the adsorption kinetics of Cu(2+) is found to follow a pseudo-second-order kinetic model. Equilibrium data for Cu(2+) adsorption are fitted well by Langmuir isotherm model. The maximum adsorption capacity for Cu(2+) ions is estimated to be 47.2 mg/g at 25 degrees C. Furthermore, thermodynamic parameters reveal the feasibility, spontaneity and exothermic nature of the adsorption process. FTIR and XPS reveal that Cu(2+) adsorption onto CMCD-MNPs mainly involves the oxygen atoms in CM-beta-CD to form surface-complexes. In addition, the copper ions can be desorbed from CMCD-MNPs by citric acid solution with 96.2% desorption efficiency and the CMCD-MNPs exhibit good recyclability. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1177 / 1186
页数:10
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