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Efficient activation of intercalated persulfate via a composite of reduced graphene oxide and layered double hydroxide
被引:32
作者:

Huang, Xin
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Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China

Su, Qingqing
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Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China

Han, Shaohong
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Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China

Zhou, Jizhi
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h-index: 0
机构:
Shanghai Univ, Sch Econ, Shanghai 200444, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China

Qian, Guangren
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Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China

Gao, Naiyun
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h-index: 0
机构:
Tongji Univ, State Key Lab Pollut Control & Resource Reuse, Shanghai 200092, Peoples R China Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
机构:
[1] Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
[2] Shanghai Univ, Sch Econ, Shanghai 200444, Peoples R China
[3] Tongji Univ, State Key Lab Pollut Control & Resource Reuse, Shanghai 200092, Peoples R China
基金:
美国国家科学基金会;
关键词:
Peroxydisulfate;
Graphene;
Layered double hydroxide;
Sulfate radical;
HETEROGENEOUSLY CATALYZED PERSULFATE;
INDUCED DEGRADATION;
ADVANCED OXIDATION;
BENZOIC-ACID;
AZO-DYE;
PEROXYMONOSULFATE;
HEAT;
SULFATE;
WATER;
RADICALS;
D O I:
10.1016/j.jhazmat.2020.122051
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Efficient activation of peroxydisulfate (PDS, S2O82-) was achieved in this study by a hybrid of reduced graphene oxide (rGO) and layered double hydroxide (LDH). The peroxydisulfate was intercalated into the interlayers of LDH that was combined with rGO. This sample contributed to 92.4 % of phenol (PhOH) removal at 25 degrees C with a PDS loading amount of 0.4 mmol/g, which is better than its LDH-PDS counterpart. A high activation of PDS in rGO/LDH-PDS was also observed during the oxidation of 4-bromophenol (4-BrPhOH), 2,4-dibromophenol (2, 4-BrPhOH), 2,6-dibromophenol (2, 6-BrPhOH) and bisphenol A (BPA). As a redox reaction of PDS in LDH, this result determined that the composite of rGO/LDH caused more PDS to be activated than LDH. As the defective rGO sites activated the PDS on the surface or edges of LDH layers, the breaking of the O-O bond in PDS generated SO4 center dot- radicals from intercalated peroxydisulfate. This result was supported by the radical scavenger experiment, electron paramagnetic resonance measurements, and the increased number of oxygen functional groups in the reacted rGO. Our work thus provided a novel strategy for PDS activation to use in environmental remediation.
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