Please use this identifier to cite or link to this item: https://idr.nitk.ac.in/jspui/handle/123456789/9633
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPrabhu, K.B.
dc.contributor.authorSaidutta, M.B.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorKamath, G.
dc.date.accessioned2020-03-31T06:51:14Z-
dc.date.available2020-03-31T06:51:14Z-
dc.date.issued2017
dc.identifier.citationJurnal Teknologi, 2017, Vol.79, 6, pp.1-9en_US
dc.identifier.uri10.1111./jt.v79.10534
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/9633-
dc.description.abstractA new chitosan derivative was prepared by grafting a ligand [3-(4methoxyphenyl)-1H-pyrazole-4-carbaldehyde] to chitosan by a Schiff base reaction. The chitosan-ligand derivative (CTSL) was characterized by spectral studies (FT-IR,13C NMR, XRD) and scanning electronic microscope. The suitability of CTSL as an adsorbent for the removal of two metals viz. Cu (II) and Pb (II) was studied by conducting equilibrium, kinetic and thermodynamic studies. Experimental data obtained in equilibrium studies were analyzed for Langmuir, Freundlich, and Redlich-Peterson isotherms. The maximum monolayer adsorption capacity obtained for the two metals were CTSL-Cu (40.62 mg/g) and CTSL-Pb (71.99 mg/g). The data obtained from the kinetic study was analyzed with three models viz. pseudo-first order, pseudo-second order and intraparticle diffusion models. The pseudo-second-order rate equation fitted the experimental data very well. Thermodynamic parameters ?G, ?H and ?S were determined. The sorption operation was feasible, exothermic and accompanied with a positive increase in entropy. The metal interactions with the adsorbent were attributed to the hydroxyl, imine and the amine groups present in the synthesized derivative. 2017 Penerbit UTM Press. All rights reserved.en_US
dc.titleA new chitosan biopolymer derivative for the removal of copper (II) and lead (II) from aqueous solutions: Synthesis, characterization and adsorption studiesen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.