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

被引:267
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
相关论文
共 64 条
[11]   Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons [J].
Duan, Xiaoguang ;
Sun, Hongqi ;
Kang, Jian ;
Wang, Yuxian ;
Indrawirawan, Stacey ;
Wang, Shaobin .
ACS CATALYSIS, 2015, 5 (08) :4629-4636
[12]   Degradation of 4-chlorophenol using catalyzed peroxymonosulfate with nano-MnO2/UV irradiation: Toxicity assessment and evaluation for industrial wastewater treatment [J].
Eslami, Akbar ;
Hashemi, Marjan ;
Ghanbari, Farshid .
JOURNAL OF CLEANER PRODUCTION, 2018, 195 :1389-1397
[13]   Manipulation of Persistent Free Radicals in Biochar To Activate Persulfate for Contaminant Degradation [J].
Fang, Guodong ;
Liu, Cun ;
Gao, Juan ;
Dionysiou, Dionysios D. ;
Zhou, Dongmei .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2015, 49 (09) :5645-5653
[14]   Key Role of Persistent Free Radicals in Hydrogen Peroxide Activation by Biochar: Implications to Organic Contaminant Degradation [J].
Fang, Guodong ;
Gao, Juan ;
Liu, Cun ;
Dionysiou, Dionysios D. ;
Wang, Yu ;
Zhou, Dongmei .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2014, 48 (03) :1902-1910
[15]   Mechanism of Base Activation of Persulfate [J].
Furman, Olha S. ;
Teel, Amy L. ;
Watts, Richard J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (16) :6423-6428
[16]   Application of peroxymonosulfate and its activation methods for degradation of environmental organic pollutants: Review [J].
Ghanbari, Farshid ;
Moradi, Mahsa .
CHEMICAL ENGINEERING JOURNAL, 2017, 310 :41-62
[17]   An effective heterogeneous iron-based catalyst to activate peroxymonosulfate for organic contaminants removal [J].
Gong, Fei ;
Wang, Lie ;
Li, Daiwen ;
Zhou, Fengya ;
Yao, Yuyuan ;
Lu, Wangyang ;
Huang, Sanqing ;
Chen, Wenxing .
CHEMICAL ENGINEERING JOURNAL, 2015, 267 :102-110
[18]   Direct reduction of iron oxides based on steam reforming of bio-oil: a highly efficient approach for production of DRI from bio-oil and iron ores [J].
Gong, Feiyan ;
Ye, Tongqi ;
Yuan, Lixia ;
Kan, Tao ;
Torimoto, Youshifumi ;
Yamamoto, Mitsuo ;
Li, Quanxin .
GREEN CHEMISTRY, 2009, 11 (12) :2001-2012
[19]   Oxidation of bromophenols by carbon nanotube activated peroxymonosulfate (PMS) and formation of brominated products: Comparison to peroxydisulfate (PDS) [J].
Guan, Chaoting ;
Jiang, Jin ;
Luo, Congwei ;
Pang, Suyan ;
Yang, Yi ;
Wang, Zhen ;
Ma, Jun ;
Yu, Jing ;
Zhao, Xi .
CHEMICAL ENGINEERING JOURNAL, 2018, 337 :40-50
[20]   Influence of pH on the Formation of Sulfate and Hydroxyl Radicals in the UV/Peroxymonosulfate System [J].
Guan, Ying-Hong ;
Ma, Jun ;
Li, Xu-Chun ;
Fang, Jing-Yun ;
Chen, Li-Wei .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2011, 45 (21) :9308-9314