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Adsorptive-Oxidative Removal of Sulfides from Water by MnO(2)-Loaded Carboxylic Cation Exchangers

Hybrid ion exchangers (HIX) containing manganese(IV) oxide (MnO(2)) based on macroporous and gel-type carboxylic cation exchangers as supporting materials were obtained. The hybrid materials were characterized using scanning electron microscopy with energy dispersive spectrometry (SEM/EDS), Fourier...

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Detalles Bibliográficos
Autores principales: Wilk, Łukasz J., Ciechanowska, Agnieszka, Kociołek-Balawejder, Elżbieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696700/
https://www.ncbi.nlm.nih.gov/pubmed/33202896
http://dx.doi.org/10.3390/ma13225124
Descripción
Sumario:Hybrid ion exchangers (HIX) containing manganese(IV) oxide (MnO(2)) based on macroporous and gel-type carboxylic cation exchangers as supporting materials were obtained. The hybrid materials were characterized using scanning electron microscopy with energy dispersive spectrometry (SEM/EDS), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD) and nitrogen adsorption isotherms at 77 K and mercury porosimetry. HIX with introduced MnO(2) (20.0–32.8 wt% Mn) were tested for removal of dissolved sulfides from anoxic aqueous solutions with 100–500 mg S(2−)/dm(3) concentrations. The process proceeded effortlessly at pH 10–13 despite unfavorable electrostatic interactions of the reactants. The highest exhibited sorption capacity was 144.3 ± 7.1 mg S(2−)/g. Approximately 65% of dissolved sulfides were oxidized to S(2)O(3)(2−) ions and repelled from HIX structure. On average, 13% of sulfide removal products were adsorbed by the MnO(2) surface. The impact of MnO(2) load and the ionic form of HIX functional groups on removal of sulfides and resulting products was examined. The mechanism of the process is suggested.