Sulfate saturated biosorbent-derived Co-S@NC nanoarchitecture as an efficient catalyst for peroxymonosulfate activation

被引:366
作者
Du, Weiyan [1 ,2 ]
Zhang, Qingzhu [2 ]
Shang, Yanan [1 ]
Wang, Wei [2 ]
Li, Qian [1 ]
Yue, Qinyan [1 ]
Gao, Baoyu [1 ]
Xu, Xing [1 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Shandong Key Lab Water Pollut Control & Resource, 27 Shanda South Rd, Jinan 250100, Shandong, Peoples R China
[2] Shandong Univ, Environm Res Inst, 27 Shanda South Rd, Jinan 250100, Shandong, Peoples R China
关键词
Nitrogen doped carbon martix; S doped Co3O4; Peroxymonosulfate; Dinotefuran; Density functional theory; DOPED CARBON NANOTUBES; BISPHENOL-A; ORGANIC POLLUTANTS; POROUS CARBON; HETEROGENEOUS ACTIVATION; OXIDATIVE-DEGRADATION; REMOVAL; WATER; PERSULFATE; GRAPHENE;
D O I
10.1016/j.apcatb.2019.118302
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using sulfate saturated bio-sorbent and cobalt(II) acetate as precursors, the homogeneous assembly of S-Co3O4 in nitrogen doped carbon martix (Co-S@NC) was obtained for the first time in an one-step pyrolysis. The reactions between peroxymonosulfate (PMS) and Co-S@NC for dinotefuran (DIN) decomposition were investigated. Co3O4 in Co@NC were primarily coordinated with the pyridinic N as catalytic sites. The adsorbed sulfate as S dopant was incorporated into the Co3O4 in carbon matrix due to the role of N as anchors, and the DIN decomposition of S-doped samples increased by 1.71 times as compared to the S-free sample (Co@NC). S incorporation can promote the formation of non-radical O-1(2) and various radicals. In addition, DFT calculations indicated the enhanced electronic conductivity after S incorporation, which would facilitate the DIN decomposition in Co-S@NC/PMS system. This work enables the first insight into the role of adsorbed sulfate as effective S dopant for PMS activation.
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页数:14
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