Abstract

Layered double hydroxide composites for water treatment have been widely studied for their advantages of high adsorption capacity, stability, and reusability. However, little is known about the co-adsorption potential and mechanism of these composites for ammonium and nitrate. In this study, based on the Box-Behnken response surface optimization design, the MgAl-layered double hydroxide@zeolite (MgAl-LDH@zeolite) composite that can rapidly co-adsorption ammonium and nitrate was synthesized via a two-step modification method. The co-adsorption process quickly reached equilibrium within 10–30 min and achieved over 80% efficiency in the initial 3 min. Besides, the MgAl-LDH@zeolite showed a low pH dependence in a wide pH range (4–8). The physico-chemical structure of MgAl-LDH@zeolite was characterized, and on this basis, the effects of pH, dosage, and coexisting ions on co-adsorption were investigated. Ion exchange, electrostatic attraction, hydrophobic sorption, and metal-bonded bridges contributed substantially to the immobilization. The ions competition simulation experiments and five regenerative cycle experiments adequately demonstrated the high selective adsorption ability and recyclability of the MgAl-LDH@zeolite. In addition, the adsorption efficiency of ammonium and nitrate in natural river water were both above 97.62%, which further confirming the application potential of the MgAl-LDH@zeolite. Overall, this work presents a new multifunctional adsorbent for nitrogen removal in the micro-polluted source water.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.