Competitive biosorption of lead, cadmium, copper, and arsenic ions using algae

The present study aims to evaluate the competitive biosorption of lead, cadmium, copper, and arsenic ions by using native algae. A series of experiments were carried out in a batch reactor to obtain equilibrium data for adsorption of single, binary, ternary, and quaternary metal solutions. The bioso...

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Published inEnvironmental science and pollution research international Vol. 20; no. 5; pp. 3011 - 3023
Main Authors Sulaymon, Abbas H., Mohammed, Ahmed A., Al-Musawi, Tariq J.
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 01.05.2013
Springer Nature B.V
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Summary:The present study aims to evaluate the competitive biosorption of lead, cadmium, copper, and arsenic ions by using native algae. A series of experiments were carried out in a batch reactor to obtain equilibrium data for adsorption of single, binary, ternary, and quaternary metal solutions. The biosorption of these metals is based on ion exchange mechanism accompanied by the release of light metals such as calcium, magnesium, and sodium. Experimental parameters such as pH, initial metal concentrations, and temperature were studied. The optimum pH found for removal were 5 for Cd 2+ and As 3+ and 3 and 4 for Pb 2+ and Cu 2+ , respectively. Fourier transformation infrared spectroscopy analysis was used to find the effects of functional groups of algae in biosorption process. The results showed that Pb 2+ made a greater change in the functional groups of algal biomass due to high affinity to this metal. An ion exchange model was found suitable for describing the biosorption process. The affinity constants sequence calculated for single system was K Pb > K Cu > K Cd > K As ; these values reduced in binary, ternary, and quaternary systems. In addition, the experimental data showed that the biosorption of the four metals fitted well the pseudo-second-order kinetics model.
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Responsible editor: Elena Maestri
ISSN:0944-1344
1614-7499
DOI:10.1007/s11356-012-1208-2