کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
55442 | 47053 | 2012 | 7 صفحه PDF | دانلود رایگان |
In order to study the intrinsic particle size effect of Co catalysts in Fischer–Tropsch (FT) synthesis, a series of Co/SiO2 model catalysts with various metal coverages (0.25–6.0 ML), corresponding to sizes in the range of 1.4–10.5 nm were prepared in an ultrahigh vacuum chamber and tested at 513 K under atmospheric pressure in a batch reactor. The Co particle size distribution and the number of active sites were estimated from the TEM images. Kinetic data and post-reaction XPS spectra showed that for the small Co particles (1.4–2.5 nm), the Co surface was readily oxidized by water vapor, while for the relatively large Co particles (3.5–10.5 nm), such oxidation was not evident. The oxidation for the small Co particles leads to lower TOF and higher CH4 selectivity, while both reactivity and selectivity were relatively constant for the relatively large Co particles. The lack of intrinsic particle size effect for the metallic Co particles in the range of 3.5–10.5 nm is consistent with structure insensitivity in FT synthesis.
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► XPS study on the cobalt Fischer–Tropsch (F–T) synthesis catalysts.
► Co/SiO2 model catalysts with monodispersed Co particles in the range of 1.4–10.5 nm.
► The rather small Co particles (1.4–2.5 nm) were oxidized by water vapor product.
► No particle size effects in F–T for the relatively large Co particles (3.5–10.5 nm).
► The importance of exploring the particle size effect on the well-defined surface.
Journal: Catalysis Today - Volume 181, Issue 1, 12 February 2012, Pages 75–81