Hydrogen production by the steam reforming of ethanol over cobalt catalysts supported on different carbon nanostructures

被引:28
|
作者
Augusto, Bruno Lobato [1 ,6 ]
Ribeiro, Mauro Celso [2 ]
Aires, Francisco J. Cadete Santos [3 ,4 ]
da Silva, Victor Teixeira [1 ]
Noronha, Fabio Bellot [5 ]
机构
[1] Univ Fed Rio de Janeiro, Chem Engn Program COPPE, BR-21941972 Rio De Janeiro, Brazil
[2] Fluminense Fed Univ, Chem Dept, Rua Des Hermydio Ellis Figueira 78, BR-27213145 Volta Redonda, Brazil
[3] Univ Lyon 1, CNRS, UMR 5256, Inst Rech Catalyse & Environm Lyon, 2 Ave Albert Einstein, F-69626 Villeurbanne, France
[4] Natl Res Tomsk State Univ, Inst Smart Mat & Technol, Lab Catalyt Res, 36 Lenin Ave, Tomsk 634050, Russia
[5] Natl Inst Technol, Catalysis Div, Av Venezuela 82, BR-20081312 Rio De Janeiro, Brazil
[6] Rural Fed Univ Rio De Janeiro, Chem Engn Dept, BR-465,Km 7, BR-23897000 Seropedica, Brazil
关键词
Hydrogen production; Steam reforming of ethanol; Carbon nanotubes; Carbon nanofibers; Cobalt catalysts; IN-SITU TEMPERATURE; NANOTUBES; CO;
D O I
10.1016/j.cattod.2018.10.029
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, we studied the performance of Co catalysts supported on different carbonaceous structures (activated carbon, carbon nanofibers and carbon nanotubes) for the steam reforming of ethanol at 773 K. Co supported on activated carbon and carbon nanofiber exhibited the smallest Co particle size and the highest activity. All catalysts deactivated but the loss of activity depended on the carbon structure. Co/C and Co/CNT catalysts significantly deactivated, while only a slight decrease in activity was observed for Co/CNF. TG analysis did not detect the formation of carbon deposits. In situ XANES and EXAFS showed that Co was partially oxidized after reduction at 623 K and the catalyst was further reduced during reaction, which rules out the oxidation of the metallic particles as the reason for catalyst deactivation. TEM of the fresh and spent catalyst showed a significant growth of the particles for Co/C and Co/CNT, indicating that sintering is the main cause of catalyst deactivation. Co/CNF only slightly deactivated because Co sintering extent was low.
引用
收藏
页码:66 / 74
页数:9
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