Cobalt supported on morphologically tailored SBA-15 mesostructures: The impact of pore length on metal dispersion and catalytic activity in the Fischer–Tropsch synthesis
1%Ru–20%Co catalysts supported on wide-pore SBA-15 mesostructures having shortened pore lengths (≤1.2 μm) show enhanced metal dispersion and superior Fischer–Tropsch activity and C 5+ selectivity than the counterpart catalysts prepared on SBA-15 silicas displaying conventional morphologies with curv...
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Veröffentlicht in: | Applied catalysis. A, General General, 2009-10, Vol.367 (1), p.146-156 |
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Zusammenfassung: | 1%Ru–20%Co catalysts supported on wide-pore SBA-15 mesostructures having shortened pore lengths (≤1.2
μm) show enhanced metal dispersion and superior Fischer–Tropsch activity and C
5+ selectivity than the counterpart catalysts prepared on SBA-15 silicas displaying conventional morphologies with curved and long (>5
μm) pores.
A series of wide-pore (11
nm) SBA-15 mesostructures displaying markedly different morphologies and pore lengths (0.3–5.7
μm) have been applied as support for 1
wt%Ru–20
wt%Co catalysts. Additionally, a reference catalyst supported on conventional narrow (7
nm)-pore SBA-15 displaying high pore length (6.9
μm) has also been synthesized. The catalytic supports and metal-loaded catalysts have been characterized by ICP-OES, N
2-physisorption, SEM, TEM, XRD, H
2-chemisorption, H
2-TPR and TPO-MS, and evaluated for the Fischer–Tropsch synthesis (FTS) under realistic conditions (
T
=
493
K,
P
=
2.0
MPa,
X
CO
=
55%). During calcination of catalyst precursors, the deleterious effect of the
endo-generated nitrate-derived gaseous oxidants (NO
2, N
2O) on metal dispersion is diminished in short-pore catalysts due to a shorter pore-residence time, as suggested by TPO-MS. Besides, during H
2 reduction, not only the
d(Co
3O
4) but also the porous structure affects the H
2-TPR profile for the catalysts, suggesting a higher pore-residence time for the formed water leading to a significant metal sintering for long-pore catalysts. Pore length is shown to be more influent than pore diameter (PD
=
7–11
nm) on the attained metal dispersion. Due to its effect on metal dispersion, at constant PD
=
11
nm, shortening the SBA-15 pores to ≤1.2
μm leads to 50–67% higher initial FTS Co-time-yields than for catalysts with conventional morphology (pore length >5
μm). As a result of these higher initial rates, due to a
d(Co
0) around the optimal 10
nm, and a lower rate loss during the transitory state (TOS
=
0–6
h), short-pore SBA-15 catalysts display very high steady cobalt-time-yields of >250
×
10
−3
mol
CO/g
Co
h. Besides, enhanced selectivity toward the desired C
5+ hydrocarbons is obtained with short-pore RuCo/SBA-15 catalysts likely due to a lower diffusional barrier for CO to the active sites. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2009.08.003 |