Environmental Research Institute, North Highland College, University of the Highlands and Islands, Thurso, Caithness, Scotland, KW14 7JD, UK; University of Novi Sad, Faculty of Technical Sciences, Department of Environmental Engineering and Occupational Safety and Health, Trg Dositeja Obradovića 6, 21 000, Novi Sad, Serbia.
School of Chemistry, University of Edinburgh, David Brewster Rd, Edinburgh, EH9 3FJ, UK.
Water Res. 2020 Apr 15;173:115573. doi: 10.1016/j.watres.2020.115573. Epub 2020 Jan 31.
Phosphorous (P) recovery from wastewater will become increasingly vital in the future as terrestrial rock phosphate deposits are expended. Effective management of P as a critical resource will require new techniques to recover P from wastewater, ideally in a form that can be used in agriculture as fertiliser. In this study, batch and fixed-bed column conditions were tested using a novel KOH deacetylated calcite-chitosan based adsorbent (CCM) for P removal from aqueous solutions and wastewater effluents. The unique characteristics of this adsorbent as a phosphate adsorbent were the result of rich surface functionality (amine and sulphur functional groups of the chitosan and proteins) and the CaCO content (providing donor ligands; and additionally beneficial if the material were used as fertiliser, buffering soil acidification caused by nitrogen application). The maximum P adsorption capacity was determined to be 21.36 mgP/g (at 22 °C) and the endodermic process reached equilibrium after 120 min. The experimental data was best described using a Langmuir isotherm and a pseudo-second order kinetic model. The diffusion kinetic analysis highlighted the importance of both film and intraparticle mass-transport. Material characterisation suggested that the adsorption process involved interactions between P and functional groups (mostly -NH) due to electrostatic interaction on the chitosan chain or involved ligand exchange with CO. Analysis of materials using X-Ray Powder Diffraction (XRPD) and Thermogravimetric Analysis (TGA) indicated a microprecipitation-type mechanism may occur through the formation of hydroxylapatite (Ca(PO)(OH)). Desorption studies demonstrated that the P-laden CCM (derived from crab carapace) had the potential to be reused in soil amendment as a slow-release P fertiliser. The effects of different operating parameters were explored in a fixed-bed column, and the experimental data fitted well to the Clark model (R = 0.99). The CCM also showed excellent P adsorption potential from secondary and final wastewater effluent in dynamic conditions, even at low P concentrations. Finally, a scale-up approach with cost analysis was used to evaluate the price and parameters needed for a potential large-scale P recovery system using this adsorbent.
随着陆地磷矿储量的消耗,未来从废水中回收磷将变得越来越重要。有效管理磷作为一种关键资源,需要新技术从废水中回收磷,理想情况下是以可作为肥料施用于农业的形式。在这项研究中,使用一种新型的 KOH 去乙酰化方解石-壳聚糖基吸附剂(CCM),通过批处理和固定床柱条件测试了从水溶液和废水废水中去除磷的方法。这种吸附剂作为一种磷酸盐吸附剂的独特特性是由于其丰富的表面功能(壳聚糖和蛋白质的胺和硫官能团)和 CaCO3 含量(提供供体配体;如果该材料被用作肥料,还可以缓冲因施氮引起的土壤酸化)。确定最大磷吸附容量为 21.36 mgP/g(在 22°C 时),并且在 120 分钟后内扩散过程达到平衡。实验数据最适合使用 Langmuir 等温线和拟二级动力学模型进行描述。扩散动力学分析突出了膜和颗粒内传质的重要性。材料特性表明,吸附过程涉及 P 与功能基团(主要是-NH)之间的相互作用,这是由于壳聚糖链上的静电相互作用或与 CO 的配体交换。使用 X 射线粉末衍射(XRPD)和热重分析(TGA)对材料进行分析表明,可能通过形成羟基磷灰石(Ca(PO)(OH))发生微沉淀型机制。解吸研究表明,负载 P 的 CCM(源自蟹壳)具有作为土壤改良剂再利用作为缓释 P 肥料的潜力。在固定床柱中探索了不同操作参数的影响,实验数据很好地符合克拉克模型(R=0.99)。在动态条件下,即使在低磷浓度下,CCM 还表现出从二级和最终废水废水中去除磷的优异吸附潜力。最后,使用成本分析的规模化方法来评估使用这种吸附剂的潜在大规模磷回收系统的价格和所需参数。