Highly Efficient AuPd/Carbon Nanotube Nanocatalysts for the Electro-Fenton Process

被引:32
作者
Sun, Meng [1 ,3 ]
Zhang, Gong [1 ,3 ]
Liu, Yang [2 ]
Liu, Huijuan [1 ]
Qu, Jiuhui [1 ]
Li, Jinghong [2 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Drinking Water Sci & Technol, Beijing 100085, Peoples R China
[2] Tsinghua Univ, Beijing Key Lab Microanalyt Methods & Instrumenta, Dept Chem, Beijing 100084, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
electro-Fenton process; gold; nanotubes; palladium; supported catalysts; BORON-DOPED DIAMOND; MANUFACTURING WASTE-WATER; OXYGEN REDUCTION REACTION; AU-PD NANOALLOYS; CARBON NANOTUBES; H2O2; OXIDATION; DEGRADATION; KINETICS; REMOVAL;
D O I
10.1002/chem.201406676
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of novel nanocatalysts for the highly efficient in situ synthesis of H2O2 from H-2 and O-2 in the electro-Fenton (EF) process has potential for the remediation of water pollution. In this work, AuPd/carbon nanotube (CNT) nanocatalysts were successfully synthesized by the facile aggregation of AuPd bimetals on CNTs. Characterization by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy indicated that pure AuPd bimetallic heterogeneous nanospheres (approximate to 20 nm) were well dispersed outside the CNTs, which resulted in better catalytic performance than Pd/CNTs alone: 0.36 M H2O2 was synthesized; 0.05 M Fe2+ optimally initiated the EF process due to the superior in situ Fe2+ regeneration; and the organic pollutant removal reached 100% at 37 min, with a pseudo-firstorder kinetic constant k(1)=0.051 min(-1). Moreover, structural insights before/after catalysis revealed that Au strengthened the construction of the nanocrystals, avoided negative deactivation caused by AuPd agglomeration, and immobilized the active Pd(111). The catalytic stability of AuPd/CNTs over ten cycles implied long durability and promising applications of this material.
引用
收藏
页码:7611 / 7620
页数:10
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