Arsenate adsorption by Mg/Al-NO3 layered double hydroxides with varying the Mg/Al ratio
Journal
Applied Clay Science
Journal Volume
43
Journal Issue
1
Pages
79-85
Date Issued
2009
Author(s)
Abstract
Arsenate is one of the main contaminants threatening water supplies all over the world. Layered double hydroxides (LDHs) have large surface areas and high anion exchange capacities, so they may be used to develop rapid and cost-effective methods for scavenging As from contaminated water. In order to enhance arsenate adsorption of layered double hydroxides, it is essential to have a fundamental understanding of the interactions between arsenate and LDHs. In this study, the effects of layer charge density and interlayer nitrate orientation of Mg/Al-NO3 LDHs on the preferential adsorption of arsenate were investigated. Mg/Al-NO3 LDHs with a Mg:Al ratio of 2:1, 3:1 and 4:1 were synthesized, using a constant-pH co-precipitation method. The adsorption maxima of As on 2:1, 3:1 and 4:1 LDHs were 1.56, 1.08 and 0.36 mmol g- 1, respectively, following the order of their layer charge densities. In addition, nitrate orientation in the LDHs plays a significant role in determining arsenate adsorption. The low arsenate adsorption of 4:1 LDH relative to its anion exchange capacity resulted from the low degree of access arsenate has to the interlayer space, so that arsenate adsorption largely occurred on the external surface of the material. The accessibility of the interlayer of 4:1 LDH to arsenate was restricted by the small basal spacing as a result of the parallel orientation of the interlayer nitrate with respect to the hydroxide sheets. Conversely, interlayer nitrate with an orientation perpendicular to the hydroxide sheets in 2:1 and 3:1 LDHs can be exchanged for arsenate more readily. Consequently, these two LDHs exhibit greater arsenate adsorption capacity, because arsenate can be adsorbed on both their external and interlayer surfaces. The arsenate adsorption of the LDHs also was highly dependent upon the type and concentration of competing anions. The negative effect of the competing anions on arsenate adsorption by various LDHs generally followed the order H2PO4- > HCO3- > SO42- > F- > Cl-. Due to the difference in adsorption mechanism, the arsenate adsorption of 4:1 LDH is subject to the negative impact of competing anions to a greater extent than those of 3:1 and 2:1 LDH. These results demonstrated that the preferential adsorption of arsenate by LDHs is dependent upon the nitrate orientation in these materials, as a consequence of changing layer charge density. The selective retention of arsenate for wastewater treatment can be maximized by controlling the orientation of interlayer nitrate in Mg/Al-NO3 LDHs. © 2008 Elsevier B.V. All rights reserved.
Subjects
Adsorption; Arsenate; Layer charge density; Layered double hydroxide
SDGs
Other Subjects
Arsenic; Charge density; Ion exchangers; Ions; Negative ions; Nitrates; Nitrogen removal; Oxides; Polyvinyl alcohols; Precipitation (chemical); Surfaces; Wastewater; Wastewater reclamation; Wastewater treatment; Water pollution; Water supply; Water treatment; Adsorption maximums; Adsorption mechanisms; All over the worlds; Anion exchanges; Arsenate; Arsenate adsorptions; Basal spacings; Contaminated waters; External surfaces; External-; Inter-layers; Interlayer spaces; Interlayer surfaces; Large surface areas; Layer charge density; Layered double hydroxide; Layered double hydroxides; Low degrees; Negative impacts; Parallel orientations; Precipitation methods; Preferential adsorptions; Selective retentions; Adsorption; adsorption; arsenate; cation exchange capacity; hydroxide; layered medium; nitrate (inorganic salt); pH; precipitation (chemistry)
Type
journal article