The synthesis of large crystals of zeolite Y re-visited

The major synthesis routes described in the literature so far for zeolite Y (FAU) with an elevated n(si)/n(Al)-ratio and larger crystallite sizes were systematically re-investigated. Syntheses in the presence of triethanolamine with or without added bis(2-hydroxyethyl)dimethylammonium chloride yielded large crystals (10-100 mu m) of faujasite-type zeolites. However, only products with low n(si)/n(Al)-ratios below 1.8 were obtained, and zeolite P was an inevitable side product or even the main product. Furthermore, the outcome of these syntheses was poorly reproducible. Following another known literature procedure, phase-pure zeolite Y could be obtained with the cyclic polyether 15-crown-5 as a structure-directing agent. The influence of ageing, homogenization and seeding of the synthesis gel, the crystallization time and temperature, different Si- and Al-sources and the addition of NaF as a mineralizer or of co-templates such as triethanolamine, ethylene glycol or 1,3,5-trioxane on the resulting product was investigated. A carefully optimized procedure led to large crystals of highly phase-pure zeolite Y with well defined octahedral morphology and a narrow crystal size distribution in the range of 4-5 mu m. Such crystals can be reproducibly synthesized in high yields with an nsi/nAl-ratio of 3.4-4.0. Neither crystallization seeds nor an ageing of the synthesis gel before hydrothermal crystallization are required. (c) 2005 Elsevier Inc. All rights reserved.