Preparation, characterization, adsorption kinetics and thermodynamics of novel magnetic chitosan enwrapping nanosized γ-Fe2O3 and multi-walled carbon nanotubes with enhanced adsorption properties for methyl orange

被引:355
作者
Zhu, H. Y. [1 ,2 ]
Jiang, R. [2 ,3 ]
Xiao, L. [1 ]
Zeng, G. M. [3 ]
机构
[1] Wuhan Univ, Coll Resource & Environm Sci, Key Lab Biomass Resource Chem & Environm Biotech, Wuhan 430072, Peoples R China
[2] Taizhou Univ, Coll Life Sci, Taizhou 317000, Peoples R China
[3] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Chitosan; Multi-walled carbon nanotubes; Magnetic gamma-Fe2O3; Methyl orange; Adsorption; AQUEOUS-SOLUTION; DYES; COMPLEX; WATER; IONS; IMMOBILIZATION; NANOPARTICLES; RECOVERY; REMOVAL; TIO2;
D O I
10.1016/j.biortech.2010.01.107
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
A novel magnetic composite bioadsorbent composed of chitosan wrapping magnetic nanosized gamma-Fe2O3 and multi-walled carbon nanotubes (m-CS/gamma-Fe2O3/MWCNTs) was prepared under relative mild conditions and was characterized. Adsorption of methyl orange (MO) onto m-CS/gamma-Fe2O3/MWCNTs was investigated with respect to pH, initial MO concentration, coexisting anions and temperature. Results of characterizations indicated that magnetic nanosized gamma-Fe2O3 and MWCNTs have been wrapped by crosslinked chitosan. Introduction of MWCNTs could obviously increase the adsorption capacity (q(e)) of MO onto bioadsorbent by 2.2 times. Kinetics data and adsorption isotherm were better fitted by pseudo-second-order kinetic model and by Langmuir isotherm, respectively. Values of activation parameters such as free energy (Delta G degrees), enthalpy (Delta H degrees) and entropy (Delta S degrees) were determined as 3.15-3.78 kJ mol(-1), -9.94 kJ mol(-1) and 20.65 J mol(-1) k(-1), respectively, indicating that the adsorption was feasible, spontaneous and exothermic process in nature. After adsorption, m-CS/gamma-Fe2O3/MWCNTs could be effectively and fleetly separated by applying a magnetic field. (C) 2010 Published by Elsevier Ltd.
引用
收藏
页码:5063 / 5069
页数:7
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