4.7 Article

Modification of chitosan macromolecule and its mechanism for the removal of Pb(II) ions from aqueous environment

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 136, Issue -, Pages 177-188

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2019.06.016

Keywords

ACSSB@ZnO; Pb(II); Kinetics; Isotherms; Thermodynamics

Funding

  1. National Natural Science Foundation of China [U1501231]
  2. Project of Guangdong Provincial Key Laboratory of Radioactive Contamination Control and Resources [2017B030314182]
  3. Science and Technology Program of Guangzhou, China [201804020072]

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It is well-known that heavy metals are non-biodegradable and have been showing remarkable impacts on the environment, public health and economics. Because of high toxic tendency, lead (Pb), is one of the foremost considerable hazardous metal with high environmental impacts. Chitosan is a polysaccharide, and can be utilized in wastewater treatment because of its good sorption ability. Amino and hydroxyl groups (C-3 position) on chitosan can serve as electrostatic interaction and complexation sites for metal cations. Chemical crosslinking can effectively enhance the stability of chitosan in acidic media. Hence a novel, cost-effective and eco-friendly ZnO incorporated into aminated chitosan Schiffs base (ACSSB@ZnO) has been synthesized, characterized (BET, XRD, FTIR, SEM, TEM and H-1 NMR), and utilized as an adsorbent for the removal of Pb(II) ions from the aqueous environment. The various operating parameters, such as pH (2-8), agitation speed (30-180), adsorbent dose (0.1-0.8 g), contact time (0-140 min), metal ion concentration and temperature (303-323 K) were investigated. The maximum sorption capacity of Pb(II) onto ACSSB@ZnO was found to be 55.55 mg/g. The equilibrium, and kinetic studies suggested that the adsorption process followed the Langmuir isotherm and Pseudo-Second-Order model. Thermodynamic data showed that the sorption process was feasible, spontaneous, and endothermic. (C) 2019 Published by Elsevier B.V.

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