TY - JOUR
T1 - Porous N-doped carbon nanospheres with encapsulated cobalt nanocrystals for persulfate activation to degrade tetracycline
AU - Wang, Min
AU - Mei, Yu
AU - Chen, Silu
AU - Komarneni, Sridhar
AU - Ma, Jianfeng
N1 - Funding Information:
This work was supported by “Qing Lan Project” of Jiangsu Province , “333 Project” of Jiangsu Province, Postgraduate Research & Practice Innovation Program of Jiangsu Province ( SJCX22_1394 ), the Natural Science Foundation of Zhejiang Province (No. LGF20E020002 ), One of us (SK) was supported by the College of Agricultural Sciences under Station Research Project No. PEN04705.
Funding Information:
This work was supported by “Qing Lan Project” of Jiangsu Province, “333 Project” of Jiangsu Province, Postgraduate Research & Practice Innovation Program of Jiangsu Province (SJCX22_1394), the Natural Science Foundation of Zhejiang Province (No. LGF20E020002), One of us (SK) was supported by the College of Agricultural Sciences under Station Research Project No. PEN04705.
Publisher Copyright:
© 2022 Elsevier Ltd and Techna Group S.r.l.
PY - 2022/10/1
Y1 - 2022/10/1
N2 - Metal-based nitrogen-doped carbon (M-N-C) materials have attracted wide attention owing to their effectiveness in activating persulfate (PS) for remediation of organic pollutants. Herein, we report a simple method of pyrolysis and simultaneous self-reduction for preparing porous N-doped carbon nanospheres encapsulated with cobalt nanocrystals (Co/p-CN) as a composite catalyst for PS activation. Co/p-CN composite was characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The composite exhibits a high surface area and rich mesoporous structure, which is conducive to exposing more active sites and facilitating mass transport of the matrix. N-doped carbon nanospheres were used to protect the cobalt nanocrystals and N doping helped to fix the Co metal through coordination for manipulating its catalytic activity. After systematic study on the preparation conditions of Co/p-CN composite, it was found that the best Co/p–CN–900 (pyrolyzed at 900 °C) could efficiently degrade tetracycline (TC) in 40 min. The quenching experiments showed that Co species in porous N-doped carbon nanospheres caused the oxidation through radicals and nonradicals (SO4•−, •OH, O2•− and 1O2) in the presence of PS. PS activation of Co/p–CN–900 composite involved the mediated electron-transfer for disintegration of refractory organic TC.
AB - Metal-based nitrogen-doped carbon (M-N-C) materials have attracted wide attention owing to their effectiveness in activating persulfate (PS) for remediation of organic pollutants. Herein, we report a simple method of pyrolysis and simultaneous self-reduction for preparing porous N-doped carbon nanospheres encapsulated with cobalt nanocrystals (Co/p-CN) as a composite catalyst for PS activation. Co/p-CN composite was characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The composite exhibits a high surface area and rich mesoporous structure, which is conducive to exposing more active sites and facilitating mass transport of the matrix. N-doped carbon nanospheres were used to protect the cobalt nanocrystals and N doping helped to fix the Co metal through coordination for manipulating its catalytic activity. After systematic study on the preparation conditions of Co/p-CN composite, it was found that the best Co/p–CN–900 (pyrolyzed at 900 °C) could efficiently degrade tetracycline (TC) in 40 min. The quenching experiments showed that Co species in porous N-doped carbon nanospheres caused the oxidation through radicals and nonradicals (SO4•−, •OH, O2•− and 1O2) in the presence of PS. PS activation of Co/p–CN–900 composite involved the mediated electron-transfer for disintegration of refractory organic TC.
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U2 - 10.1016/j.ceramint.2022.06.058
DO - 10.1016/j.ceramint.2022.06.058
M3 - Article
AN - SCOPUS:85132717130
SN - 0272-8842
VL - 48
SP - 27622
EP - 27630
JO - Ceramics International
JF - Ceramics International
IS - 19
ER -