4.7 Article

Insight into the roles of endogenous minerals in the activation of persulfate by graphitized biochar for tetracycline removal

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 768, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.144281

Keywords

Biochar; Deashing; Mineral; Co-pyrolysis; Persulfate; Tetracycline degradation

Funding

  1. Major Science and Technology Program for Water Pollution Control and Treatment [2017ZX07301006004]
  2. Natural Science Foundation of Guangdong Province [2017A030313239]
  3. Research Project of Sino-Singapore international joint research institute [202-A018001]
  4. Ministry of Science and Technology of China for State Key Research and Development Project [2016YFC04007082]
  5. Student Research Project of South China University of Technology [7387]
  6. State Key Laboratory of Pollution Control and Resource Reuse [PCRRF14006, PCRRF17018]
  7. National Key Research and Development Program of China [2019YFA0210400]

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The study showed that the natural endogenous minerals in biochar can promote the formation of porous and defective structures, increase carbonization and graphitization degree, and exhibit higher catalytic efficiency in the activation of persulfate for tetracycline degradation.
Owing to its environmental-friendliness, low-cost, and outstanding characteristics, biochar has been widely used for the catalytic degradation of various organic pollutants. In this study, a pre- and post-deashing graphitized biochar (DBC800 and PBC800-A) was prepared and compared with the pristine biochar (PBC800) to activate persulfate (PS) for tetracycline (TC) degradation. The influence of the natural endogenous mineral on the catalytic ability of biochar was investigated. Characterization results show that the inherent endogenous mineral in biochar not only acted as a natural pore-forming agent to promote the formation of the porous structure, but also facilitated the formation of edge defective structures, and altered the surface functional groups, as well as increased the carbonization and graphitization degree of biochar. The PBC800-A exhibited a much higher catalytic efficiency on PS activation and TC oxidative degradation with the reaction rate of 0.06055 min(-1), 7.14 times as that of DBC800 (0.00861 min(-1)) and 4.63 times as that of PBC800 (0.00158 min(-1)). The endogenous minerals were conducive to the generation of free radicals and promoted the oxidative degradation of TC. which was mainly attributed to the improved carbon configuration. The post-deashing treatment was also found to significantly improve the electron transport efficiency of biochar by removing the residual ash, thereby promoting the generation of singlet oxygen. This study demonstrated that the natural minerals in biochar was beneficial for the degradation of TC, and more alternative natural minerals can be applied to co-pyrolysis with biochar for the re- mediation of refractory organic pollutants. (C) 2020 Elsevier B.V. All rights reserved.

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