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Sulfated Zirconia with Ordered Mesopores as an Active Catalyst for n-Butane Isomerization

MPG-Autoren
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Yang,  Xiaobo
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Jentoft,  Friederike C.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Jentoft,  Rolf E.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Ressler,  Thorsten
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Zitation

Yang, X., Jentoft, F. C., Jentoft, R. E., Girgsdies, F., & Ressler, T. (2002). Sulfated Zirconia with Ordered Mesopores as an Active Catalyst for n-Butane Isomerization. Catalysis Letters, 81(1-2), 25-31. doi:10.1023/A:1016095603350.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0011-1475-F
Zusammenfassung
Zirconia/surfactant composites were hydrothermally synthesized in aqueous sulfuric acid at 373 K using Zr(O-nPr)4 as oxide precursor and hexadecyl-trimethyl-ammonium bromide (CTAB) as template. Mesostructural features similar to those of MCM-41 were detected by X-ray diffractometry, with d = 4.6 nm. A sample obtained from a starting mixture with Zr:S:CTAB = 2:2:1 was stable enough for removal of occluded organics. After calcination at 813 K, the d-value was 3.6 nm, the surface area 200 m2/g, and the mean pore diameter estimated by the BJH method 2.2 nm. Extended X-ray absorption fine structure analysis suggests Zr to be in a short-range structure (< 4 Å) similar to that of Zr in monoclinic ZrO2. Scanning electron microscopy including energy dispersive X-ray analysis showed 1-5 µm sulfur-containing ZrO2 spheres. The material catalyzes the isomerization of n-butane to i-butane at 378 K with a steady activity in the order of magnitude of commercial sulfated ZrO2.