Enhanced visible-light-assisted peroxymonosulfate activation over MnFe2O4 modified g-C3N4/diatomite composite for bisphenol A degradation

双酚A 降级(电信) 复合数 化学 可见光谱 化学工程 核化学 材料科学 复合材料 有机化学 计算机科学 光电子学 电信 工程类 环氧树脂
作者
Xiangwei Zhang,Chunquan Li,Ting Chen,Ye Tan,Xiaorui Liu,Fang Yuan,Shuilin Zheng,Zhiming Sun
出处
期刊:International journal of mining science and technology [Elsevier BV]
卷期号:31 (6): 1169-1179 被引量:62
标识
DOI:10.1016/j.ijmst.2021.11.008
摘要

The MnFe2O4/g-C3N4/diatomite composites (Mn/G/D) were prepared via a facile precipitation-calcination method in this study. The Mn/G/D possessed higher specific surface area, lower electron-hole pairs' recombination rate, as well as wider and stronger visible light absorption capacity. Since the synergistic effect between g-C3N4 and MnFe2O4, the photogenerated electron could transfer from g-C3N4 to MnFe2O4, which could promote the migration of electrons as well as enhance the photocatalytic activity and peroxymonosulfate (PMS) activation efficiency. Mn/G/D-5% composite displayed the excellent degradation performance of bisphenol A (BPA) with the removal efficiency of 99.9% under PMS/Vis system, which was approximately 2.47 and 63.8 times as high as that of the Mn/G/D-5%/PMS and Mn/G/D-5%/Vis system, respectively. Moreover, negative electricity derived from diatomite surface also promoted the photogenerated carriers' migration, and the degradation rate constant was around 2.4 times higher than that of MnFe2O4/g-C3N4 (Mn/G). In addition, quenching experiments showed that both radical pathway (h+, ·OH, ·O2− and SO4·−) and non-radical pathway (1O2) were responsible for the degradation of BPA.
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