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Adsorption kinetics and environmental impact mechanisms of schwertmannite on phosphorus
Received:July 25, 2024  
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KeyWord:schwertmannite;phosphorus;dynamic representation;adsorption mechanism;influencing factor
Author NameAffiliationE-mail
Dudagula Inner Mongolia Ecological Environment Inspection Technical Support Center, Hohhot 010011, China  
SONG Wenjie Pioneer College, Inner Mongolia University, Hohhot 010000, China  
XIE Zhilei Inner Mongolia Environmental Monitoring Station, Hohhot 010011, China  
LI Hao School of Ecology and Environment, Inner Mongolia University, Hohhot 010021, China  
LI Zhichao School of Ecology and Environment, Inner Mongolia University, Hohhot 010021, China  
HE Jiang School of Ecology and Environment, Inner Mongolia University, Hohhot 010021, China ndjhe@imu.edu.cn 
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Abstract:
      To explore the adsorption mechanism of schwertmannite(SCH)for PO43- and the possibility of its application as a PO43- adsorbent, this study focuses on the adsorption behavior of SCH towards PO43-, employing continuous characterization of SCH throughout the process as a means to investigate its adsorption kinetics for PO43-. The study also discusses the impact of pH and the competitive adsorption of As(Ⅲ) and Cr(Ⅵ)ions on SCH′s ability to adsorb PO43-, thereby revealing the underlying mechanism governing SCH′s affinity for PO43-. The findings indicate that the adsorption of PO43- by SCH follows quasi-second-order kinetics and a three-stage intraparticle diffusion model, with chemical adsorption being the primary mechanism within a non-homogeneous diffusion process. The equilibrium adsorption capacity within 24 hours can reach 17.38 mg·g-1. We observed that PO43- can interact with SCH through ligand exchange and ion exchange processes. Specifically, OH groups on the surface of SCH are preferentially involved in ligand exchange with PO43-, followed by ion exchange with SO42- within SCH, both mechanisms contributing to enhanced stability. Continuous characterization results further revealed the generation of secondary minerals such as water iron during the process of PO43- adsorption by SCH. Furthermore, we found that As(Ⅲ)competes for adsorption sites with PO43-, thus inhibiting its uptake by SCH; conversely, Cr(Ⅵ)promotes the adsorption of PO43- by providing additional binding sites, and alkaline conditions were shown to be more conducive to effective PO43- adsorbing performance by SCH.