TY - JOUR
T1 - Cobalt-doped g-C 3 N 4 as a heterogeneous catalyst for photo-assisted activation of peroxymonosulfate for the degradation of organic contaminants
AU - Wang, Lingli
AU - Guo, Xu
AU - Chen, Yingying
AU - Ai, Shasha
AU - Ding, Hanming
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/2/15
Y1 - 2019/2/15
N2 - Cobalt-mediated peroxymonosulfate (PMS) activation is an effective way to generate sulfate radicals for the degradation of pollutants. Herein, a heterogeneous Co-based catalyst was prepared by integrating the cobalt species to the cavities of g-C 3 N 4 via the Co–N bonds through the methods of impregnation and calcination, which was applied to activate PMS for the degradation of organic contaminates under visible light. The cobalt species were atomically dispersed on g-C 3 N 4 , which could provide more reactive sites for PMS activation. The catalytic efficiency of cobalt-doped g-C 3 N 4 was greater than that of pure g-C 3 N 4 or even slightly higher than that of the homogeneous cobalt ions during the photo-assisted PMS activation catalytic processes. The optimum Co loading is 1.0% in weight. In 25 min, the dye of rhodamine B was almost completely degraded with a 70.5% of total organic carbon (TOC) removal under its natural pH value in the presence of such catalytic system. The enhanced catalytic activity of Co-doped g-C 3 N 4 was due to the effective separation of the photo-generated charges as well as the sufficient accessible reactive sites for PMS activation. And the synergistic interaction between the photocatalytic and PMS activation processes facilitated the generation of active species for the removal of pollutants.
AB - Cobalt-mediated peroxymonosulfate (PMS) activation is an effective way to generate sulfate radicals for the degradation of pollutants. Herein, a heterogeneous Co-based catalyst was prepared by integrating the cobalt species to the cavities of g-C 3 N 4 via the Co–N bonds through the methods of impregnation and calcination, which was applied to activate PMS for the degradation of organic contaminates under visible light. The cobalt species were atomically dispersed on g-C 3 N 4 , which could provide more reactive sites for PMS activation. The catalytic efficiency of cobalt-doped g-C 3 N 4 was greater than that of pure g-C 3 N 4 or even slightly higher than that of the homogeneous cobalt ions during the photo-assisted PMS activation catalytic processes. The optimum Co loading is 1.0% in weight. In 25 min, the dye of rhodamine B was almost completely degraded with a 70.5% of total organic carbon (TOC) removal under its natural pH value in the presence of such catalytic system. The enhanced catalytic activity of Co-doped g-C 3 N 4 was due to the effective separation of the photo-generated charges as well as the sufficient accessible reactive sites for PMS activation. And the synergistic interaction between the photocatalytic and PMS activation processes facilitated the generation of active species for the removal of pollutants.
KW - Atomically dispersion
KW - Chemical coordination
KW - Cobalt
KW - Degradation mechanism
KW - Photo-assisted peroxymonosulfate activation
UR - https://www.scopus.com/pages/publications/85055916148
U2 - 10.1016/j.apsusc.2018.10.262
DO - 10.1016/j.apsusc.2018.10.262
M3 - 文章
AN - SCOPUS:85055916148
SN - 0169-4332
VL - 467-468
SP - 954
EP - 962
JO - Applied Surface Science
JF - Applied Surface Science
ER -