Search results for "Carbonium ion"
showing 4 items of 4 documents
A kinetic study of the cracking, isomerization, and disproportionation of n-heptane on a chromium-exchanged Y zeolite
1982
The kinetic rate constants for the cracking, isomerization, and disproportionation of n-heptane over a CrHNaY (32% chromium exchanged) zeolite catalyst at 400, 450, and 470 °C have been calculated. The interaction of n-heptane with a model Lewis acid such as BF3 and progress along the reaction coordinate have been studied by means of molecular orbital calculations. From the kinetic results, i.e., activation energies and frequency factors, and the theoretical calculations, it can be concluded that the controlling step in these reactions is not the formation of the carbonium ion, but the subsequent transformation of this carbonium ion. In addition, the theoretical calculations show that the a…
Hydrocracking ofn-heptane. Study of NiO-MoO3catalysts supported on a HY ultrastable zeolite
1986
The hydrocracking of n-heptane in the temperature range of 573 to 623 K and at 2.45 × 106 Pa pressure has been employed as a test reaction for the study of Ni—Mo bifunctional catalysts supported on a HY ultrastable zeolite. Two groups of catalysts containing 8 and 12 wt% of MoO3 and different amounts of NiO have been studied. In both series a maximum in the activity has been obtained for catalysts with a Ni/Mo atomic ratio of 0.8-1.0. The order of the impregnation of the oxides can have little influence on the activity. The most active catalyst has been obtained when the zeolite is exchanged with NH+4 ions until the Na+ level is less than 2% of the original and calcined at 823 K to obtain a…
Complex Metabolic Activation Pathways of Polycyclic Aromatic Hydrocarbons: 3-Hydroxy-trans-7,8-Dihydroxy-7,8-Dihydrobenzo[a]Pyrene as a Proximate Mut…
1988
3-Hydroxybenzo[a]pyrene (3-OH-BP) is a major metabolite of benzo[a]pyrene (BP) in various systems. Metabolites of 3-OH-BP, formed by liver enzymes, bind to DNA1,2 and are mutagenic3,4. However, the active species have not yet been identified. Administration of 3-OH-BP to rats results in the excretion of sulfate and glucuronic acid conjugates of 3-hydroxy-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene (3-OH-BP-7,8-diol) (Fig. 1) as major metabolites in the bile5. The hydroxyl groups of this triol are structurally superimposable to those of 9-hydroxy-trans-1,2-dihydroxy-1,2-dihydrochrysene (9-hydroxychrysene-1,2-diol, Fig. 1), which is a metabolite of chrysene6,7 and a potent promutagen8,9. 9-…
On the potential carcinogenic and mutagenic character of benzobiphenylenes
1979
Abstract PMO estimations suggest certain partially saturated benzobiphenylene carbonium ions might exhibit carcinogenic and/or mutagenic activity.