TY - JOUR
T1 - Effect of pH and Calcium on the Adsorptive Removal of Cadmium and Copper by Iron Oxide–Coated Sand and Granular Ferric Hydroxide
AU - Uwamariya, V.
AU - Petrusevski, B.
AU - Lens, P. N. L.
AU - Amy, Gary L.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors thank the Netherlands Government for providing financial assistance through the Netherlands Fellowship Program for the financial support under Grant No. 32000022.
PY - 2015/8/17
Y1 - 2015/8/17
N2 - Iron oxide-coated sand (IOCS) and granular ferric hydroxide (GFH) were used to study the effect of Ca2+ and pH on the adsorptive removal of Cu2+ and Cd2+ from groundwater using batch adsorption experiments and kinetic modeling. It was observed that Cu2+ and Cd2+ were not stable in synthetic waters. The extent of precipitation increased with increasing pH. Removal of Cu2+ and Cd2+ was achieved through both precipitation and adsorption, with IOCS showing higher adsorption efficiency. Increase of pH (from 6 to 8) resulted in a higher overall removal efficiency of both Cu2+ and Cd2+, with precipitation as predominant removal mechanisms at higher pH values, especially for Cu2+. An increase in Ca2+ concentration increased the precipitation of Cu2+ [as Cu2(OH)2CO3 and Cu3(OH)2(CO3)2] and Cd2+ [as Cd(OH)2 and CdCO3]. In addition, Ca2+ competes with Cu2+ and Cd2+ for surface adsorption sites on IOCS and GFH, and reduces their adsorption capacity. The kinetic modeling revealed that the adsorption of Cd2+ onto IOCS is a complex process, with limited contribution of chemisorption that increases in the presence of Ca2+. © 2015 American Society of Civil Engineers.
AB - Iron oxide-coated sand (IOCS) and granular ferric hydroxide (GFH) were used to study the effect of Ca2+ and pH on the adsorptive removal of Cu2+ and Cd2+ from groundwater using batch adsorption experiments and kinetic modeling. It was observed that Cu2+ and Cd2+ were not stable in synthetic waters. The extent of precipitation increased with increasing pH. Removal of Cu2+ and Cd2+ was achieved through both precipitation and adsorption, with IOCS showing higher adsorption efficiency. Increase of pH (from 6 to 8) resulted in a higher overall removal efficiency of both Cu2+ and Cd2+, with precipitation as predominant removal mechanisms at higher pH values, especially for Cu2+. An increase in Ca2+ concentration increased the precipitation of Cu2+ [as Cu2(OH)2CO3 and Cu3(OH)2(CO3)2] and Cd2+ [as Cd(OH)2 and CdCO3]. In addition, Ca2+ competes with Cu2+ and Cd2+ for surface adsorption sites on IOCS and GFH, and reduces their adsorption capacity. The kinetic modeling revealed that the adsorption of Cd2+ onto IOCS is a complex process, with limited contribution of chemisorption that increases in the presence of Ca2+. © 2015 American Society of Civil Engineers.
UR - http://hdl.handle.net/10754/621796
UR - http://ascelibrary.org/doi/10.1061/%28ASCE%29EE.1943-7870.0001009
UR - http://www.scopus.com/inward/record.url?scp=84983042479&partnerID=8YFLogxK
U2 - 10.1061/(asce)ee.1943-7870.0001009
DO - 10.1061/(asce)ee.1943-7870.0001009
M3 - Article
SN - 0733-9372
VL - 142
JO - Journal of Environmental Engineering
JF - Journal of Environmental Engineering
IS - 9
ER -