Abstract
Chronic exposure to Pb2+ above the 15-μg/L US Environmental Protection Agency action level for drinking water has been shown to cause a host of health problems in humans. Thus, it is important to study new methods available for the treatment and removal of Pb2+ from drinking water and wastewater, where elevated levels of heavy metals are found. Alginate-based beads represent one such possible method for heavy metal removal. The impact of alginate density on the equilibrium and kinetics of Pb2+ sorption onto hydrogel beads was investigated using Ca-alginate beads ranging from 1% to 8% (w/v) and exposed to Pb2+ concentrations ranging from 100 to 1,000 mg/L. When Ca-alginate beads were characterized using Fourier transform infrared analysis, the carboxylic acid groups of the mannuronate and guluronate residues in alginate were the primary functional groups that interacted with Pb2+. Hydration of Ca-alginate beads was also examined and found to decrease as Ca-alginate density increased. A positive correlation was observed between Ca-alginate hydration and Pb2+ sorption. Sorption of Pb2+ was fast, reaching equilibrium after approximately 4 h, and is well described by the Langmuir adsorption isotherm. Maximum sorption capacities for 1%, 4%, and 8% beads were 500 ± 100, 360 ± 30, and 240 ± 20 mg/g (dry weight), respectively. The kinetics of sorption were best described by the pseudo-second-order Lagergren model, with rate constants determined as 3.2 ± 0.1 × 10−4, 1.0 ± 0.1 × 10−4, and 1.6 ± 0.1 × 10−4 g mg−1 min−1 for 1%, 4%, and 8% beads, respectively.
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Acknowledgement
This research was funded by the Jerome A. Schiff Fellowship (Wellesley College) and the Merck/AAAS Undergraduate Science Research Program awarded to Wellesley College. The authors thank Ms. Lauren F. Allison for help with some measurements on the hydrogel beads.
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Stewart, T.J., Yau, JH., Allen, M.M. et al. Impacts of calcium-alginate density on equilibrium and kinetics of lead(II) sorption onto hydrogel beads. Colloid Polym Sci 287, 1033–1040 (2009). https://doi.org/10.1007/s00396-009-2058-4
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DOI: https://doi.org/10.1007/s00396-009-2058-4