High efficient removal of bisphenol A in a peroxymonosulfate/iron functionalized biochar system: Mechanistic elucidation and quantification of the contributors

被引:255
作者
Jiang, Shun-Feng [1 ]
Ling, Li-Li [1 ]
Chen, Wen-Jing [1 ]
Liu, Wu-Jun [1 ]
Li, De-Chang [1 ]
Jiang, Hong [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, CAS Key Lab Urban Pollutant Convers, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Peroxymonosulfate; Nonradical pathway; Bisphenol A; Fe biochar composite; Quantification; ACTIVATED PERSULFATE OXIDATION; METAL-ORGANIC FRAMEWORKS; PERSISTENT FREE-RADICALS; ZERO-VALENT IRON; PHOTOCATALYTIC DEGRADATION; HETEROGENEOUS CATALYSIS; MAGNETIC NANOPARTICLES; ENHANCED ACTIVATION; HYDROXYL RADICALS; HIGH ADSORPTION;
D O I
10.1016/j.cej.2018.11.124
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Activation of peroxymonosulfate (PMS) to degrade recalcitrant organic pollutants has attracted much attention, however, this process usually needs expensive or toxic catalysts. Herein, we prepared a Fe functionalized biochar composite that contain Fe-0, porous carbon with abundant functional groups and nanofibers (Fe-BC-700) to activate PMS and efficiently remove bisphenol A (BPA). The contribution of different participants in the complicated system involving Fe species, carbon composites, and radicals and nonradicals were quantitatively investigated. Under optimal conditions (0.2 g/L PMS and 0.15 g/L catalyst), 20 mg/L of BPA can be completely removed in 5 min by Fe-BC-700. The effects including the activation of PMS by Fe species to produce sulfate radicals (SO4 center dot-), the electron transfer by the nanofiber-mesoporous carbon structure, and the inherent persistent free radicals (PFR) in biochar, were demonstrated to contribute to the high performance. A series of contrast experiments showed that PMS activated by Fe contributed to about 36% of BPA degradation, while the carbon composites, especially carbon nanofibers contributed to 17%, and the other 47% was ascribed to the adsorption of carbon composites (may further undergoing degradation). Meanwhile, the degradation by SO4 center dot- accounted for about 23% (by quenching experiments), while the nonradical pathway contributed to 30%. This work suggests that the non-activation factors in PMS/porous catalyst/pollutant system cannot be neglected.
引用
收藏
页码:572 / 583
页数:12
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