Cargando…

Magnetic Beads of Zero Valent Iron Doped Polyethersolfun Developed for Removal of Arsenic from Apatite-Soil Treated Water

The drop immerses calcium chloride aqueous solution was utilized to prepare the zero valent iron-doped polyethersulfone beads (PES/ZVI) for the efficient removal of arsenic from apatite-soil treated waters. The proposed beads can assist in promoting uptake efficiency by hindering ZVI agglomeration d...

Descripción completa

Detalles Bibliográficos
Autores principales: Noorbakhsh, Roya, Koohi, Mohammad Kazem, Hassan, Jalal, Rahmani, Anosheh, Rashidi Nodeh, Hamid, Rezania, Shahabaldin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9566726/
https://www.ncbi.nlm.nih.gov/pubmed/36231997
http://dx.doi.org/10.3390/ijerph191912697
Descripción
Sumario:The drop immerses calcium chloride aqueous solution was utilized to prepare the zero valent iron-doped polyethersulfone beads (PES/ZVI) for the efficient removal of arsenic from apatite-soil treated waters. The proposed beads can assist in promoting uptake efficiency by hindering ZVI agglomeration due to a high porosity and different active sites. The PES/ZVI beads were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and vibrating sample magnetism (VSM). The main objective of this study was to investigate the function of new PES/ZVI beads with an increased removal efficiency for the remediation of arsenic ions from the apatite-soil treated waters. A maximum adsorption removal of 82.39% was achieved when the experiment was performed with 80 mg of adsorbent for a contact time of 180 min. Based on the results, a removal efficiency >90% was obtained after 300 min of shaking time with an arsenic concentration of 20 mg·L(−1). The experimental process was fitted with the Langmuir model due to the high R(2) (0.99) value compared to the Freundlich model (0.91) with an adsorption capacity of 41.32 mg·g(−1). The adsorption process speed was limited by pseudo-second-order (R(2) = 0.999) and the adsorption mechanism nature was endothermic and physical.