Transport-limited kinetics of phosphate retention on iron-coated sand and practical implications

• Published in: Journal of contaminant hydrology 2023-04, Vol.255, p.104160-104160, Article 104160
• Main Authors: Barcala, Victoria, Zech, Alraune, Osté, Leonard, Behrends, Thilo
• Format: Article
• Language: English
• Subjects: Adsorption; Iron; Kinetics; Mitigation measures; Phosphates; Phosphorous; Phosphorus sorbing materials; Reactive transport model; Recycled iron oxides; Sand; Water Pollutants, Chemical - analysis; Water treatment residuals
• ISSN: 0169-7722; 1873-6009
• DOI: 10.1016/j.jconhyd.2023.104160

Iron-coated sand (ICS) is a by-product from drinking water treatment made of sand coated with ferric iron (hydr)oxides. It is considered a suitable material for large-scale measures for phosphate removal from natural and agricultural waters to prevent eutrophication. Previous studies demonstrated that the residence time of water must be very long to reach equilibrium partitioning between phosphate and ICS but specifics for application are missing. First, SEM-EDX images were used to support the conceptual assumption that P adsorption inside the coating is a transport-limited process. Second, a conceptual model of phosphate adsorption was proposed considering two types of sites: one type with fast adsorption kinetics and reaching equilibrium with the percolating solution, and another type for which adsorption is also reversible but described by pseudo-first-order kinetics. The latter is conceived to account for transport-limited adsorption in the interior of the coating while the former fraction of sites is assumed to be easily accessible and located close to the grain surface. Third, the kinetics of phosphate adsorption on ICS were quantitatively determined to describe and predict phosphate retention in filters under various flow conditions. The model was calibrated and validated with long-term column experiments, which lasted for 3500 h to approach equilibrium on the slowly reacting sites. The model reproduced the outflowing phosphate concentrations: the pronounced increase after a few pore volumes and the slow increase over the remaining part of the experiment. The parameterized model was also able to predict the time evolution of phosphate concentrations in the outflow of column experiments with different flow velocities, flow interruption, and in desorption experiments. The equilibrium partition coefficient for the experimental conditions was identified as 28.1 L/g-Fe at pH 6.8 and a phosphate concentration of 1.7 mg-P / L. The optimized first-order mass transfer coefficient for the slow adsorption process was 1.56 10−4 h−1, implying that the slow adsorption process has a time scale of several months. However, based on the parameterized model, the slow adsorption process accounted for 95.5% of the equilibrium adsorption capacity, emphasizing the potential relevance of this process for practical applications. The implications for the design, operation, and lifespan of ICS filters are exemplarily illustrated for different scenarios. [Display omitted] •The