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Beta-zeolite structural properties and activity and selectivity for catalytic cracking

Conference · · American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA)
OSTI ID:5283647
; ; ;  [1]
  1. Instituto de Catalisis y Petroleoquimica, Madrid (Spain)
A series of beta-zeolites has been synthesized in the presence of tetraethylammonium hydroxide (TEAOH). Samples with Si/A1 ratio in the 8-106 range have been characterized by X-ray powder diffraction, i.r. spectroscopy and pyridine adsorption. It has been found that a fraction of the tetraethylammonium (TEA) ion is compensating the charge of the framework aluminium atoms, and it is removed at temperature higher than a second fraction of TEA which is occluded in the structure. Calcination of the samples at temperatures > 550{degree}C causes the formation of structural defects or the breaking of crystallites, with the corresponding increase in the number of silanol groups (3740 cm{sup {minus}1}, i.r. band). Hydroxyl bands at 3615 and 3680 cm{sup {minus}1} are observed, the first being much more intense and directly proportional to the number of framework aluminiums. Pyridine interacts strongly with the 3615 cm{sup {minus}1} band, hydroxyls, and weakly with the 3680 cm{sup {minus}1} ones. Deepbed calcination of the samples produces a decrease in the intensity of the 3615 cm{sup {minus}1} band, probably due to partial dealumination; the presence of pyridine bonded to Lewis acid sites is an agreement with this assumption. Comparison of the catalytic properties of H-beta and HY zeolites for cracking n-heptane and gas oil show that beta-zeolite should have more than one type of channel, with different dimensions. For gas-oil cracking, beta-zeolite is less active and produces more coke and less gasoline than HY zeolite.
OSTI ID:
5283647
Report Number(s):
CONF-8708311--
Conference Information:
Journal Name: American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA) Journal Volume: 32:3
Country of Publication:
United States
Language:
English