Abstract

Ce Al and La Al pillared bentonites were prepared by cation-exchange of different bentonites with hydrothermally treated (130–160°C for 16–136 h) solutions containing mixtures of aluminiumchlorohydrate (ACH) and REE (Ce and La)-salts. After calcination at 500°C the pillared clays are characterised by basal spacings of 24.8–25.7 Å, and have BET surface areas of approximately 430 m 2/g. The pillared products are hydrothermally stable to at least 500°C. The large basal spacings and surface areas are due to the formation of large REE/Al containing polyoxycations. The formation of this cation is favoured by high initial Al concentrations (≥3.7 M) and an OH Al molar ratio of approximately 2.5. Ce Al or La Al ratios can be as low as 1 30 . Hydroconversion of n-heptane indicated that the activity of these materials is higher than that of a conventional Pt loaded amorphous silica alumina (ASA) reference catalyst. The selectivity is strongly dependant on the type of starting clay. In industrial hydrocracking of normal feedstock, a Ni W loaded REE/Al pillared clay catalyst showed slightly higher initial activity than the ASA reference catalyst. However, the pillared clay catalyst showed rapid deactivation due to coke-formation, which reduced the surface area and pore volume. Additionally coke formation may be facilitated by the relatively high iron content of the pillared bentonite (3.43 wt%).

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