Abstrakti
Isomerization of n-butane over Pt ion-exchanged H-MCM-41 catalyst was studied with varying weight hour space velocities and reactant flow dilutions by using hydrogen or nitrogen as carrier gases. As a comparison, H-MCM-41 was evaluated in n-butane transformations, but it did not exhibit any activity. The main products over Pt-H-MCM-41 were methane, ethane, propane, butenes, isobutane and negligible amounts of other products, indicating that hydrogenolysis was taking place to large extent. The absence of pentanes and a low selectivity to propane as products suggests that dimerization-cracking pathway did not occur. Rather high amounts of isobutane are probably formed parallel to hydrogenolysis via a monomolecular pathway following a bifunctional mechanism. This involves butane dehydrogenation to linear butene, isomerization of linear butene to isobutene followed by hydrogenation of isobutene to isobutane.
| Alkuperäiskieli | Englanti |
|---|---|
| Sivut | 15-19 |
| Sivumäärä | 5 |
| Julkaisu | Catalysis Communications |
| Vuosikerta | 5 |
| Numero | 1 |
| DOI - pysyväislinkit | |
| Tila | Julkaistu - tammik. 2004 |
| OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |
Rahoitus
This work is part of the activities at the Åbo Akademi Process Chemistry Centre within the Finnish Centre of Excellence Programme (2000–2005) by the Academy of Finland. Financial support from Fortum Foundation to V.N. is gratefully acknowledged.
Sormenjälki
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