Separation and preconcentration of some heavy-metal ions using new chelating polymeric hydrogels

Two new chelating polymeric hydrogels, crosslinked polyacrylamide/triethylenetetraamine/CS₂Na (hydrogel I) and crosslinked polyacrylamide/diethylenetriamine/CS₂Na (hydrogel II), were prepared by the transamidation and dithiocarbamylation of crosslinked polyacrylamide. The products were characterized...

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Published inJournal of applied polymer science Vol. 113; no. 2; pp. 1335 - 1344
Main Authors Sharaf, Mohamed A, Arida, Hassan A, Sayed, S.A, Younis, Ahmed A, Farag, A.B
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.07.2009
Wiley
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Summary:Two new chelating polymeric hydrogels, crosslinked polyacrylamide/triethylenetetraamine/CS₂Na (hydrogel I) and crosslinked polyacrylamide/diethylenetriamine/CS₂Na (hydrogel II), were prepared by the transamidation and dithiocarbamylation of crosslinked polyacrylamide. The products were characterized with elemental analysis and IR spectroscopy. In both polymeric hydrogels, the optimum pH for the removal of Cd(II), Pb(II), and Zn(II) ions ranged from 7 to 8, from 6 to 7, and from 7 to 8, respectively. The sorption isotherms of the investigated metal ions on the prepared hydrogels were developed, and the equilibrium data fitted the Langmuir and Freundlich isotherm models well. At the optimum pH for each metal ion, the maximum sorption capacities of hydrogel I toward Cd(II), Pb(II), and Zn(II) ions, estimated from the Langmuir model, were 5.3, 0.63, and 1.27 mmol/g, respectively, and those of hydrogel II were 4.1, 0.59, and 0.89 mmol/g, respectively. The experimental sorption capacities of hydrogel I toward Cd(II), Pb(II), and Zn(II) ions were 4.5, 0.6, and 1.2 mmol/g, respectively. In the case of hydrogel II, the capacities were 3.7, 0.52, and 0.88 mmol/g in the same prescribed order. The thermodynamic parameters (the free energy of sorption, enthalpy change, and entropy change) for cadmium, lead, and zinc sorption on the prepared polymers were also determined from the temperature dependence.
Bibliography:http://dx.doi.org/10.1002/app.30137
ArticleID:APP30137
U.S.-Egypt Science and Technology (Joint Fund) - No. MA7-001-002
istex:EEA93CAC7B4369D0EB0D075058AB0C455CB5552D
National Science Foundation - No. INT-9605191; No. INT-01-11334
ark:/67375/WNG-Z98N2X9T-X
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0021-8995
1097-4628
1097-4628
DOI:10.1002/app.30137