Effect of pore size distribution and particle size of porous metal oxides on phosphate adsorption capacity and kinetics
AuthorsKumar, Prashanth Suresh
Keesman, Karel J.
van Loosdrecht, Mark C. M.
Witkamp, Geert Jan
KAUST DepartmentBiological and Environmental Science and Engineering (BESE) Division
Environmental Science and Engineering Program
Water Desalination and Reuse Research Center (WDRC)
Permanent link to this recordhttp://hdl.handle.net/10754/670050
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AbstractPhosphate is a vital nutrient but its presence in surface waters even at very low concentrations can lead to eutrophication. Adsorption is often suggested as a step for reducing phosphate down to very low concentrations. Porous metal oxides can be used as granular adsorbents that have a high surface area and hence a high adsorption capacity. But from a practical point of view, these adsorbents also need to have good adsorption kinetics. The surface area of such adsorbents comes from pores of varying pore size and the pore size distribution (PSD) of the adsorbents can affect the phosphate adsorption kinetics. In this study, the PSD of 4 different adsorbents was correlated with their phosphate adsorption kinetics. The adsorbents based on iron and aluminium (hydr)oxide were grinded and the adsorption performance was studied as a function of their particle size. This was done to identify diffusion limitations due to the PSD of the adsorbents. The phosphate adsorption kinetics were similar for small particles of all the adsorbents. For larger particles, the adsorbents having pores larger than 10 nm (FSP and DD6) showed faster adsorption than adsorbents with smaller pores (GEH and CFH). Even though micropores (pores < 2 nm) contributed to a higher portion of the adsorbent surface area, pores bigger than 10 nm were needed to increase the rate of adsorption.
CitationSuresh Kumar, P., Korving, L., Keesman, K. J., van Loosdrecht, M. C. M., & Witkamp, G.-J. (2019). Effect of pore size distribution and particle size of porous metal oxides on phosphate adsorption capacity and kinetics. Chemical Engineering Journal, 358, 160–169. doi:10.1016/j.cej.2018.09.202
SponsorsThis work was performed in the TTIW-cooperation framework of Wetsus, European Centre Of Excellence For Sustainable Water Technology (www.wetsus.nl). Wetsus is funded by the Dutch Ministryof Economic Affairs, the European Union Regional Development Fund,the Province of Fryslân, the City of Leeuwarden and the EZ/Kompasprogram of the“Samenwerkingsverband Noord-Nederland”. We thankthe participants of the research theme“Phosphate Recovery”for theirfinancial support and helpful discussions.
JournalCHEMICAL ENGINEERING JOURNAL