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Degradation of methyl orange by zero-valent tungsten without external oxidants
被引:0
|作者:
Xia, Tao
[1
]
Shi, Meng
[1
]
Liu, Zhongda
[1
,2
]
Yang, Miao
[1
]
机构:
[1] Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Peoples R China
[2] Univ Patras, Dept Chem Engn, Caratheodory 1St, Patras 26504, Greece
基金:
中国国家自然科学基金;
关键词:
Azo dye;
Degradation;
Methyl orange;
Tungsten;
zero-valent;
AQUEOUS-SOLUTION;
REDUCTIVE DEGRADATION;
ADVANCED OXIDATION;
IRON;
MECHANISM;
REMOVAL;
COPPER;
DECHLORINATION;
NANOPARTICLES;
TETRACYCLINE;
D O I:
10.1016/j.dwt.2024.100152
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Recently, zero-valent tungsten (W-0) has been applied as a new zero-valent metal to degrade pollutants by the activation of H2O2, peroxydisulfate and peroxymonosulfate to generate (OH)-O-center dot or SO4 center dot-. However, the direct pollutant degradation by W-0 without external oxidants has not been investigated yet. In this work, Methyl Orange was directly degraded by W-0 without any external oxidants, even dissolved oxygen. The degradation followed first-order kinetics, and k(obs) showed an approximately linear correlation with W-0 dosage. An acidic condition (pH 2) led to a higher degradation rate (0.162 min(-1)) and simultaneously a lower metal leaching (2.7 mg/L). SEM and XRD confirmed the unchanged morphology and crystalline structure of W-0 after reaction, while the oxide shell was found more stable in the acidic condition, supported by higher W6+ content observed by XPS. Both (OH)-O-center dot and O-2(center dot)- were detected by ESR, but radical scavenging experiments excluded (OH)-O-center dot as the main reactive species. By contrast, O-2(center dot)- and electrons had a higher contribution. The O-2(center dot)- was dependent on the dissolved oxygen while electrons were not, and thus the degradation occurred efficiently in the anaerobic condition. This work provides opportunities for a greener wastewater treatment process and supplementary understandings of the oxidant-involved processes.
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页数:7
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