Nanorod carbon nitride as a carbo catalyst for selective oxidation of hydrogen sulfide to sulfur

被引:44
作者
Kamali, Farnoush [1 ]
Eskandari, Mohammad Mehdi [2 ]
Rashidi, Alimorad [2 ]
Baghalha, Morteza [1 ]
Hassanisadi, Mostafa [2 ]
Hamzehlouyan, Tayebeh [1 ]
机构
[1] Sharif Univ Technol, Chem & Petr Engn Dept, POB 11365-11155, Tehran, Iran
[2] Res Inst Petr Ind, Nanotechnol Res Ctr, West Side Azadi Complex,POB 148573111, Tehran, Iran
关键词
Hydrogen sulfide; Selective catalytic oxidation; Carbo catalyst; Carbon nitride nanorod; Silica template; ACTIVATED CARBON; HIGHLY EFFICIENT; PORE STRUCTURE; SURFACE-AREA; NITROGEN; H2S; NANOTUBES; SOFT; ADSORPTION/OXIDATION; TEMPERATURE;
D O I
10.1016/j.jhazmat.2018.09.095
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Two-dimensional mesoporous carbon nitride and its highly efficient nanorod framework were prepared via hard-templating method. The obtained materials were fully characterized. The results showed that the samples structural ordering and morphology were similar to those of the parent silica templates; they had large pore volumes as well as high surface area structures. Carbon nitride carbocatalysts were used for H2S selective oxidation. The catalytic tests were carried out at 190, 210 and 230 degrees C in a fixed bed reactor. The obtained selectivity values for mesoporous carbon nitride rod and mesoporous carbon nitride toward elemental sulfur at 190 degrees C were 88.8% and 83%, respectively. Both samples were highly active due to their alkaline surface, appropriate pore size distribution and structure. In comparison with other carbon-based materials used for this process, mesoporous carbon nitride rod is the first carbonaceous material reported so far that could yield high levels of both conversion and selectivity at 190 degrees C. This superiority could be caused by the narrow pore size distribution (< 3 nm), incorporation of nitrogen into the carbon matrix and its appropriate morphology. Nitrogen species act as electron donors in H2S oxidation. Rod-like particles might have acted as nanoreactors that facilitated the reaction progress.
引用
收藏
页码:218 / 226
页数:9
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