Deciphering highly resistant characteristics to different pHs of oxygen vacancy-rich Fe2Co1-LDH/PS system for bisphenol A degradation
[Display omitted] •Novel oxygen vacancy-rich Fe2Co1-LDH was fabricated.•SO4− and OH were the main active radicals in acid and alkaline pHs, respectively.•Oxygen vacancies, transition metals, and surface hydroxyl group showed interactive function for PS activation. This first-attempt study explored i...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-04, Vol.385, p.123620, Article 123620 |
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Sprache: | eng |
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•Novel oxygen vacancy-rich Fe2Co1-LDH was fabricated.•SO4− and OH were the main active radicals in acid and alkaline pHs, respectively.•Oxygen vacancies, transition metals, and surface hydroxyl group showed interactive function for PS activation.
This first-attempt study explored interactive function of oxygen vacancies, transition metals, and surface hydroxyl groups for persulfate (PS) activation, at different pH conditions. Oxygen vacancy-rich Fe2Co1-LDHs was fabricated via calcination in hydrogen atmosphere. The Fe2Co1-LDH possessed the maximal concentration of oxygen vacancies and abundant hydroxyl groups for effective functioning according to the characterization through X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR). The BPA-degrading efficiency in the LDHs/PS system indicated that Fe2Co1-LDH exhibited the most promising activated performance since oxygen vacancies could improve the catalytic efficiency to enhance electron transport phenomena between the Fe and Co. N2 experiments proved that the presence of oxygen vacancies could promote the production of 1O2 and O2−. Phosphate and pH effect experiments showed the Fe2Co1-LDH/PS system stably maintained operation performance over a wide pH range for bisphenol A (BPA) removal with the effect of surface hydroxyl groups. Practical samples had little effect on the removal of BPA. According to the quenching experiments and EPR technology, SO4− was the main active radicals in acid and neutral conditions and apparently the OH played the crucial role at alkaline pHs. Two different major reaction routes at different pH levels in the Fe2Co1-LDH/PS system for mechanisms of BPA degradation were proposed herein. The Chemical intermediates of BPA degradation were identified by gas chromatography-mass spectrophotometry (GC–MS) analysis, and degradation pathways were proposed for system optimization. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2019.123620 |