文章摘要
都达古拉,宋文杰,谢志磊,李浩,李智超,何江.施氏矿物对磷的吸附特性[J].农业环境科学学报,2025,44(7):1848-1859.
施氏矿物对磷的吸附特性
Adsorption kinetics and environmental impact mechanisms of schwertmannite on phosphorus
投稿时间:2024-07-25  
DOI:10.11654/jaes.2024-0634
中文关键词: 施氏矿物    连续表征  吸附机理  影响机制
英文关键词: schwertmannite  phosphorus  dynamic representation  adsorption mechanism  influencing factor
基金项目:国家自然科学基金项目(32160299,42167028)
作者单位E-mail
都达古拉 内蒙古自治区生态环境督察技术支持中心, 呼和浩特 010011  
宋文杰 内蒙古大学创业学院, 呼和浩特 010000  
谢志磊 内蒙古自治区环境监测总站, 呼和浩特 010011  
李浩 内蒙古大学生态与环境学院, 呼和浩特 010021  
李智超 内蒙古大学生态与环境学院, 呼和浩特 010021  
何江 内蒙古大学生态与环境学院, 呼和浩特 010021 ndjhe@imu.edu.cn 
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中文摘要:
      为探究施氏矿物(Schwertmannite,SCH)对PO43-的吸附机理及其作为PO43-吸附剂的可能性,本研究以SCH对PO43-的吸附性能为研究主线,以全过程SCH的连续表征为手段,开展了SCH对PO43-的吸附动力学研究,讨论了pH及As(Ⅲ)和Cr (Ⅵ)等共存离子竞争吸附对SCH吸附PO43-的影响,揭示了SCH对PO43-的吸附机理及机制。研究表明:SCH对PO43-的吸附符合准二级动力学及3段式颗粒内扩散模型,以化学吸附为主且属于非均相扩散过程,24 h内的平衡吸附量可达17.38mg·g-1。PO43-可通过配体交换作用和离子交换作用与SCH结合,且PO43-优先与SCH表面的OH发生配体交换,而后再与SCH中的SO42-发生离子交换,两种吸附机制均可增强SCH的稳定性。连续表征结果表明,SCH吸附PO43-的过程中伴随有水铁矿次生矿物的生成。As(Ⅲ)通过与PO43-竞争吸附位点抑制了SCH对PO43-的吸附,而Cr (Ⅵ)则通过为PO43-开拓吸附位点的方式促进了SCH对PO43-的吸附,且碱性条件更有利于SCH对PO43-的吸附。
英文摘要:
      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.
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