Single and competitive adsorptive removal of lead, cadmium, and mercury using zeolite adsorbent prepared from industrial aluminum waste

The removal of Pb2+, Cd2+, and Hg2+, which act as endocrine disruptors, from aqueous solutions was performed using a NaP1-type zeolite synthesized from a hazardous aluminum waste. The effects of parameters such as pH, contact time, adsorbent dose, initial cation concentration, and coexisting cations...

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Bibliographic Details
Published in:Desalination and water treatment 2018-09, Vol.126, p.181-195
Main Authors: Sánchez-Hernández, Ruth, Padilla, Isabel, López-Andrés, Sol, López-Delgado, Aurora
Format: Article
Language:English
Subjects:
Adsorption kinetic
Competitive adsorption
Endocrine disruptor
Equilibrium isotherm
Heavy metal
NaP1 zeolite
Water treatment
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Summary:The removal of Pb2+, Cd2+, and Hg2+, which act as endocrine disruptors, from aqueous solutions was performed using a NaP1-type zeolite synthesized from a hazardous aluminum waste. The effects of parameters such as pH, contact time, adsorbent dose, initial cation concentration, and coexisting cations on the adsorption efficiency and capacity of the adsorbent were evaluated. Single-cation adsorption was found to be a fast process well described by the pseudo-second-order kinetic model. Equilibrium was reached in the first 15 min achieving high removal efficiencies: 98.9%, 93.3%, and 99.3% for Pb2+, Cd2+, and Hg2+, respectively. The removal of the metal cations could occur via a homogeneous and physical adsorption process that was satisfactorily described by the Sips isotherm. The maximum adsorption capacities, obtained from the Sips isotherm model, were 245.75, 4.43, and 0.22 mg/g for Pb2+, Cd2+, and Hg2+, respectively. In multi-cation adsorption, the zeolite presented the greatest affinity for Pb2+ (due to its smallest cationic size) compared with Cd2+ and Hg2+. The Pb2+ removal efficiency remained practically constant in presence of Hg2+ and Cd2+, reaching efficiencies near 100% at very low contact times (
ISSN:1944-3986
DOI:10.5004/dwt.2018.22816