Ion-exchange is an alternative process for uptake of heavy metals from aqueous solutions. In the present study, the sorption of nickel(II) ions from aqueous solution was investigated by using Lewatit MonoPlus SP 112 (strongly acidic, macroporous cation-exchange resin) in a batch adsorption system as a function of pH (2.0-8.0), initial nickel concentration (50-200 mg/L), resin dosage (0.5-2.0 g/L), contact time (0.5-3h), and temperatures (298-318K). The data were analyzed on the basis of Lagergren pseudo-first order, pseudo-second order (Types 1-5), Elovich and external, Weber-Morris intraparticle, pore-surface mass diffusion models. The experimental data showed that the maximum pH for efficient sorption of nickel(II) was 6.0. At the optimal conditions, nickel(II) ions sorption on the resin was decreased when the initial metal concentration increased. The results indicated that the resin dosage strongly affected the amount of nickel(II) ions removed from aqueous solution. The adsorption process was very fast due to 80% of nickel(II) sorption was occurred within 30 min and equilibrium was reached at about 90 min. Freundlich and Langmuir adsorption isotherm models were used for sorption equilibrium data and the maximum adsorption capacity (171 mg/g) of Lewatit MonoPlus SP 112 was obtained from Langmuir isotherm. The thermodynamic parameters (DeltaG degrees, free energy change; DeltaS degrees, enthalpy change; and DeltaH degrees, entropy change) for sorption of nickel(II) ions were evaluated. The rise in temperature caused a partly increase in the value of the equilibrium constant (K(c)) for the sorption of nickel(II) ions. Moreover, column flow adsorption study was also studied. Breakthrough curves were obtained from column flow studies by using both synthetic solution and rinsing bath water of filter industry. The column regeneration was carried out for two sorption-desorption cycles. The eluant used for regeneration of the cation-exchange resin was 7% (w/w) HCl. The experimental results demonstrated that Lewatit MonoPlus SP 112 cation-exchange resin could be used effectively for the removal of nickel(II) ions from aqueous medium.
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http://dx.doi.org/10.1016/j.jhazmat.2009.01.073 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Institut für Chemie, Humboldt-Universität zu Berlin, Brook-Taylor-Straße 2, 12489, Berlin, Germany.
Anal Methods
November 2024
Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore - 632 014, Tamil Nadu, India.
In this study, we present three different approaches for the colorimetric detection of Ni ions using a specifically designed benzothiazole-quinoline dyad (L) synthesized the Knoevenagel condensation reaction in high yield. The unique properties of L enable a rapid and selective response to Ni ions, making it an ideal probe for practical applications. The probe L shows a pale yellow color under normal conditions.
View Article and Find Full Text PDFJ Hazard Mater
November 2024
Zhejiang Key Laboratory of Petrochemical Environmental Pollution Control, Zhejiang Ocean University, Zhoushan 316022, China; National & Local Joint Engineering Research Center of Harbor Oil & Gas Storage and Transportation Technology, Zhejiang Ocean University, Zhoushan 316022, China. Electronic address:
Membrane-based electro-deposition (MED) is an original process promising for reversible removal and recovery of toxic heavy metal ions from wastewater. The removal efficiency of heavy metal ions, however, was limited by the poor membrane surface HO splitting in the conventional ion exchange membrane (IEM). Inspired by the amphoteric interface-triggered ion exchange resin regeneration phenomenon in electro-deionization, herein we subtly introduced the amphoteric group into IEM as a proof of concept to solve the above bottleneck.
View Article and Find Full Text PDFParamagnetic complexes of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate (DOTA) derivatives have shown potential for molecular imaging with magnetic resonance. DOTA-tetraglycinate (DOTA-4AmC) coordinated with lanthanide metal ions (Ln) demonstrates pH/temperature sensing with Biosensor Imaging of Redundant Deviation in Shifts (BIRDS) and Chemical Exchange Saturation Transfer (CEST), respectively, detecting nonexchangeable (e.g.
View Article and Find Full Text PDFInorg Chem
November 2024
Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, New York14260, United States.
Herein, we report the reaction between four 1,2-dibromoxylenes and two tetra-3-pyridylporphyrins for the formation of a cofacial porphyrin core spanned by dipyridinium xylene moieties. The metal-free organic nanocage (oNC) was synthesized in one twenty-four h step at a gram-scale with a 91.5% yield.
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