Abstract
Modification of a H-mordenite (HM) has been achieved by the controlled reaction of bulky organometallic complexes such as dineopentylmagnesium and tetrabutyltin with the external surface. For both complexes, the first observed reaction is a reaction of solvolysis leading to the formation of a grafted alkyl complex, i.e.→ SI-O-MgNP and →Si-O-SnBu, respectively, and to the liberation of one mole of alkane per atom M (M=Sn, Mg). Full characterization of these surface alkyl complexes has been achieved by IR, 13C MAS NMR, analysis of the evolved gases, elemental analysis. Thermal decomposition at 350°C under vacuum leads to surface oxidized (Sn(II) or Sn(IV) well dispersed on the external surface of the mordenite. These grafted mordenites mixed with a 0.5% Pt/Al2O3, exhibit higher performance in the C8 (orthoxylene+ethylbenzene) cut isomerization compared with non-modified mordenites. The activity is found to be higher and the dismutation yields have been strongly reduced, regeneration of grafted tetrabutyltin mordenite leads to additional reduction of dismutation.
Original language | English (US) |
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Journal | American Chemical Society, Division of Petroleum Chemistry, Preprints |
Volume | 36 |
Issue number | 4 |
State | Published - Aug 1991 |
Externally published | Yes |
Event | Symposium on Alkylation, Aromatization, Oligomerization and Isomerization of Short Chain Hydrocarbons over Heterogeneous Catalysts - New York, NY, USA Duration: Aug 25 1991 → Aug 30 1991 |
ASJC Scopus subject areas
- Fuel Technology