Heteroatom-Doped Carbon Nanomaterials as Metal-Free Catalysts for the Reduction of 4-Nitrophenol

被引:38
|
作者
Jarrais, Bruno [1 ]
Guedes, Alexandra [2 ,3 ]
Freire, Cristina [1 ]
机构
[1] Univ Porto, Fac Ciencias, Dept Quim & Bioquim, REQUIMTE LAQV, Rua Campo Alegre S-N, P-4169007 Oporto, Portugal
[2] Univ Porto, Fac Ciencias, Inst Cithornncias Terra, Polo FCUP, Rua Campo Alegre 687, P-4169007 Oporto, Portugal
[3] Univ Porto, Fac Ciencias, Dept Geociencias Ambiente & Ordenamento Terr, Rua Campo Alegre 687, P-4169007 Oporto, Portugal
来源
CHEMISTRYSELECT | 2018年 / 3卷 / 06期
关键词
Catalysis; Doping; Graphene flakes; Multi-walled carbon nanotubes; 4-Nitrophenol reduction; OXYGEN REDUCTION; CHEMICAL-REDUCTION; RECENT PROGRESS; GRAPHENE; NITROGEN; EFFICIENT; HYDROGENATION; BORON; ELECTROCATALYST; NITROBENZENE;
D O I
10.1002/slct.201702706
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work it is described the preparation and characterization of multi-walled carbon nanotubes and graphene flakes doped with heteroatoms, namely N, P, B, and S, through simple ball milling procedures with adequate precursors, followed by thermal treatments. Ball milling the carbon nanomaterials with melamine resulted in the introduction of pyrrolic, pyridinic and quaternary N atoms on the graphitic structure. Using triphenylphosphine as the phosphorous precursor induced the formation of R-O-PO(OH)(2) functionalities. Materials prepared with boric acid showed the presence of boronic groups (C-BO2) and B atoms in B2O3. S-doped materials presented tiophene-S type atoms. The catalytic studies showed that all the doped carbon materials were active catalysts in the reduction of 4-nitrophenol (4-NP), and that the modifications introduced by the doping procedures, overall yielded catalysts with superior activity in regard to their pristine counterparts. Reusability experiments revealed no loss of catalytic activity up to three catalytic cycles for the doped carbon nanotubes, whereas the graphene flake materials showed some deterioration of catalytic performance.
引用
收藏
页码:1737 / 1748
页数:12
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