Controllable synthesis of oxygenated carbon supported palladium nanodendrites for highly efficient nitroaromatics reduction

被引:5
|
作者
Zhao, Wen [1 ]
Wang, Tianlong [1 ]
Wang, Baoan [1 ]
Wang, Ran [1 ]
Xia, Yu [1 ]
Liu, Mengping [1 ]
Tian, Lihong [1 ]
机构
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organochem Mat, Key Lab Synth & Applicat Organ Funct Mol, Minist Educ, Wuhan 430062, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dots; Palladium nanodendrites; Nitroaromatics; Hydrogenation; MESOPOROUS CARBON; QUANTUM DOTS; CATALYTIC-ACTIVITY; AROMATIC NITRO; PHOTOCATALYTIC PERFORMANCE; SELECTIVE HYDROGENATION; SILVER NANOPARTICLES; ACTIVATED CARBONS; PD NANOPARTICLES; GRAPHENE;
D O I
10.1016/j.colsurfa.2022.130677
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
Palladium nanodendrites supported on oxygenated carbon layer (Pd/ O-carbon) have been prepared herein through modulating the mass ratio of Pd (II) precursor and carbon dots derived from sucrose without additional reducing agent. Characterizations of FT-IR, XPS spectra and TEM graphs reveal that oxygen-bearing groups on carbon dots play important role in reducing Pd(II) into Pd(0), controlling nanoparticle growth and stabilizing Pd nanodendrites. The as-prepared Pd/ O-carbon presents size-dependent activity on catalytic p-nitrophenol (4-NP) reduction using NaBH4 as hydrogen donor. The reaction rate constant of 4-NP on Pd/ O-carbon with Pd particle size of 4-7 nm almost triples that on catalyst with Pd nanoparticles of 6-10 nm. Pd / O-carbon can be reused for 10 times without obvious decreased activity, showing a long-term chemical stability in 4-NP reduction reaction. In addition, Pd / O-carbon achieves similar to 100% selectivity on nitrobenzene conversion and > 95% selectivity for the hydrogenation of substituted nitrobenzene compounds with methyl-, chloro- and amino- groups to corresponding aniline through tandem reaction with NH3BH3 as hydrogen donor in methanol/ water solvent (volume ratio of 1:3).
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页数:9
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