共 61 条
Peroxymonosulfate activation by tin(IV) phosphate supported cobalt composite for acetaminophen degradation: Performance and mechanism
被引:4
作者:

Deng, Shisi
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Shan, Zezhong
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h-index: 0
机构:
Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Zhang, Haojie
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h-index: 0
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Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Guo, Jing
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h-index: 0
机构:
Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Chen, Cheng
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h-index: 0
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Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Li, Ying
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h-index: 0
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Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China

Lan, Yeqing
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China
机构:
[1] Nanjing Agr Univ, Coll Sci, Nanjing 210095, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Tin(IV) phosphate supported cobalt composite;
Peroxymonosulfate activation;
Acetaminophen;
Catalytic degradation;
Advanced oxidation processes;
HYDROGEN PHOSPHATE;
ADVANCED OXIDATION;
WASTE-WATER;
REMOVAL;
SULFATE;
PARACETAMOL;
CATALYSTS;
EXCHANGE;
METALS;
D O I:
10.1016/j.jwpe.2024.105343
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Tin(IV) phosphate -supported cobalt composite (Co-SnP) was prepared and employed as a heterogeneous activator of peroxymonosulfate (PMS) for acetaminophen (APAP) degradation. The results indicated that almost all APAP (5 mg L -1 ) was eliminated by PMS (0.5 mM) assisted with Co-SnP (0.2 g L -1 ) in an initial pH range of 7 - 9 within 15 min, mainly owing to the role of center dot OH and SO 4- center dot , with contributions of 59.7 % and 39.6 %, respectively. The rate constant ( k ) value increased gradually with the increase in catalyst dosage and PMS concentration. APAP degradation was suppressed by Cl - , HCO 3 - and humic acid but promoted by NO 3 - . The Co-SnP/PMS system exhibited strong oxidation ability toward APAP in real water matrices and toward other organic pollutants (rhodamine B, phenacetin, bisphenol A, and sulfisoxazole), indicating the outstanding catalytic performance of Co-SnP for PMS activation. Furthermore, the superior stability and reusability of the Co-SnP catalyst were confirmed through four consecutive uses. Finally, the intermediates of APAP degradation were identified and the APAP degradation pathways were proposed. This work demonstrates the potential application of the Co-SnP/ PMS system in the elimination of organic pollutants from water and provides a novel avenue for the recovery and utilization of phosphorus and cobalt ions in wastewater.
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