کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1282969 | 1497616 | 2010 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Hydrogen production by steam reforming of acetic acid: Comparison of conventional supported metal catalysts and metal-incorporated mesoporous smectite-like catalysts Hydrogen production by steam reforming of acetic acid: Comparison of conventional supported metal catalysts and metal-incorporated mesoporous smectite-like catalysts](/preview/png/1282969.png)
The activities of various metal catalysts were tested in steam reforming of acetic acid for the production of H2, using conventional metal oxides and transition metal-incorporated mesoporous smectite-like materials as supports. It has been found that Pt is superior to Ni, Co, and Fe among Al2O3 supported catalysts, Al2O3 is more effective than ZrO2 and SiO2 as support for Pt, Ni incorporated smectite (SM(Ni)) support is more effective than Fe and Co incorporated ones for Pt, and SM(Ni) is also active in the absence of Pt. The total activity for the conversion of acetic acid is in the order of Pt/Al2O3 > Pt/SM(Ni) > SM(Ni) but the ability of H2 production is comparable among these catalysts. These catalysts (and the other ones) were observed to lose their activities during the reforming reactions. The activity of Pt/Al2O3 decreased during the whole course of reaction up to 10 h. In contrast, the activity of SM(Ni) also decreased within 2 h but it showed a stable activity in the following stage of reaction. The initial activity of the used Pt/SM(Ni) and SM(Ni) was able to be almost completely restored by thermal treatment with H2 but less effectively for the used Pt/Al2O3. The catalyst deactivation was shown to occur by the formation and deposition of carbon materials on the catalysts (XRD, TEM, thermal analysis). The properties of carbon deposits formed on Pt/Al2O3 and SM(Ni) catalysts should be different and this may be responsible for the differences in the extent of deactivation and in the regeneration behavior between the two catalysts.
Journal: International Journal of Hydrogen Energy - Volume 35, Issue 1, January 2010, Pages 110–117