In this study, four geopolymer sorbents GP0, GP10, GP30 and GP50 were synthesized using volcanic ash (VA) and metakaolin (MK) blends as precursors with 0, 10, 30 and 50% MK content by mass, respectively. The materials were characterized by X-ray fuorescence (XRF), X-ray difraction (XRD), Raman spectroscopy, and Brunauer–Emmett–Teller (BET) surface area analyses, revealing successful geopolymerization of the precursors and increasing surface area with increasing MK content. The sorption performance of the VA, MK and VA-MK geopolymers was then evaluated for the removal of cationic methylene blue (MB) dye from aqueous media. Sorption capacity was independent of composition, providing fexibility in sorbent synthesis. Sorption rate, on the other hand, was 3–8 times greater for the VA-MK geopolymers than the precursor materials. The equilibrium adsorption data were suitably explained by the Freundlich model, denoting multilayer adsorption onto a heterogeneous adsorption surface with higher Freundlich afnity constant (KF) for geopolymers than VA. The adsorption kinetics obeyed the pseudo-second-order (PSO) kinetic law with an average of 98% removal efciency in 30 min. MB uptake was pH-dependent and driven by electrostatic chemisorption interactions. These results motivate further studies on the use of locally sourced geopolymers for water purifcation applications.
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Modeling performance of rhamnolipid-coated engineered magnetite nanoparticles for U( vi ) sorption and separation
Based on tunable properties, engineered nanoparticles (NPs) hold significant promise for water treatment technologies. Motivated by concerns regarding toxicity and non-biodegradability of some nanoparticles, we explored engineered magnetite (Fe 3 O 4 ) nanoparticles with a biocompatible coating. These were prepared with a coating of rhamnolipid, a biosurfactant primarily obtained from Pseudomonas aeruginosa . By optimizing synthesis and phase transfer conditions, particles were observed to be monodispersed and stable in water under environmentally relevant pH and ionic strength values. These materials were evaluated for U( vi ) removal from water at varying dissolved inorganic carbon and pH conditions. The rhamnolipid-coated iron oxide nanoparticles (IONPs) showed high sorption capacities at pH 6 and pH 8 in both carbonate-free systems and systems in equilibrium with atmospheric CO 2 . Equilibrium sorption behavior was interpreted using surface complexation modeling (SCM). Two models (diffuse double layer and non-electrostatic) were evaluated for their ability to account for U( vi ) binding to the carboxyl groups of the rhamnolipid coating as a function of the pH, total U( vi ) loading, and dissolved inorganic carbon concentration. The diffuse double layer model provided the best simulation of the adsorption data and was sensitive to U( vi ) loadings as it accounted for the change in the surface charge associated with U( vi ) adsorption.
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- Award ID(s):
- 1704326
- PAR ID:
- 10223456
- Date Published:
- Journal Name:
- Environmental Science: Nano
- Volume:
- 7
- Issue:
- 7
- ISSN:
- 2051-8153
- Page Range / eLocation ID:
- 2010 to 2020
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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