Large pore REE/Al pillared bentonites: Preparation, structural aspects and catalytic properties

被引:38
作者
Booij, E
Kloprogge, JT
vanVeen, JAR
机构
[1] TNO,INST PHYS APPL,DEPT INORGAN MAT CHEM,NL-5600 AN EINDHOVEN,NETHERLANDS
[2] SHELL RES & TECHNOL CTR AMSTERDAM,NL-1030 BN AMSTERDAM,NETHERLANDS
[3] FREE UNIV AMSTERDAM,FAC EARTH SCI,NL-1081 HV AMSTERDAM,NETHERLANDS
关键词
aluminium; bentonite; catalysis; preparation; properties; rare earths;
D O I
10.1016/S0169-1317(96)00019-1
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ce/Al and La/Al pillared bentonites were prepared by cation-exchange of different bentonites with hydrothermally treated (130-160 degrees C for 16-136 h) solutions containing mixtures of aluminiumchlorohydrate (AGH) and REE (Ce and La)-salts. After calcination at 500 degrees C the pillared clays are characterised by basal spacings of 24.8-25.7 Angstrom, and have BET surface areas of approximately 430 m(2)/g, The pillared products are hydrothermally stable to at least 500 degrees 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 (greater than or equal to 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%).
引用
收藏
页码:155 / 162
页数:8
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