Issue 99, 2015

Simultaneous removal of nickel and phosphorus from spent electroless nickel plating wastewater via calcined Mg–Al–CO3 hydroxides

Abstract

For electroless nickel plating wastewater, a novel approach for the simultaneous removal of nickel and phosphorus on calcined Mg–Al–CO3 hydroxides (CLDHs) is proposed. The dependence of the adsorption efficiency on several parameters, including initial ions' concentration, temperature, contact time and pH, has been investigated with batch experiments. The adsorption kinetics data of nickel and phosphorus could be well depicted by a pseudo-second-order model. Adsorption isotherms studies showed that the uptake of nickel and phosphorus on CLDHs followed Langmuir and Freundlich models, respectively, and that the maximum removal of nickel or phosphorus was up to 22.87 or 761.5 mg g−1. Thermodynamic analyses implied that the adsorption process of nickel or phosphorus on CLDHs was spontaneous and endothermic. Further, the possible mechanisms were explored in: low concentration solutions, CLDHs took part in reconstitution involving the isomorphous substitution of nickel at the magnesium sites in sheets and by the concomitant utilization of phosphorus by the generated superficial sheets; and in high concentration solutions, the CLDHs rebuilding hydrotalcite structures were influenced and formed mixed metal salts of phosphites, hydroxides, and hypophosphites, which were attributed to the presence of plentiful phosphorus and brought about the reduced uptake of nickel.

Graphical abstract: Simultaneous removal of nickel and phosphorus from spent electroless nickel plating wastewater via calcined Mg–Al–CO3 hydroxides

Article information

Article type
Paper
Submitted
29 Jun 2015
Accepted
09 Sep 2015
First published
09 Sep 2015

RSC Adv., 2015,5, 80978-80989

Author version available

Simultaneous removal of nickel and phosphorus from spent electroless nickel plating wastewater via calcined Mg–Al–CO3 hydroxides

M. Sun, J. Su, S. Liu, D. Wang, W. Yan, L. Zhang, Y. Xiao and X. Gao, RSC Adv., 2015, 5, 80978 DOI: 10.1039/C5RA12570G

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