4.7 Article

Green synthesis of zeolites from a natural aluminosilicate mineral rectorite: Effects of thermal treatment temperature

Journal

APPLIED CLAY SCIENCE
Volume 90, Issue -, Pages 53-60

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.clay.2014.01.006

Keywords

Rectorite; Thermal treatment; Zeolite P; In-situ synthesis

Funding

  1. Ministry of Science and Technology of China [2010CB226905]
  2. National Natural Science Foundation of China [21276270, 20825621]
  3. Science Foundation of China University of Petroleum, Beijing [KUJJ2012-03-06]

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This article reports the effects of thermal treatment temperature on the physicochemical properties of a rectorite mineral and the chemical reactivity and crystallization behavior of the activated rectorite products for zeolite synthesis purposes. The raw rectorite mineral and its thermal activation products were systematically characterized by XRF, XRD, FTIR and Si-29 and Al-27 MAS NMR techniques and the resultant zeolites were characterized by XRD technique. The results showed that after being thermally treated in the temperature range of 25-1300 degrees C, the rectorite experienced the following four stages: dehydration at 150-300 degrees C, dehydroxylation at 600-700 degrees C, structure collapse at 1000 degrees C, and new phase formation at above 1100 degrees C. Moreover, it was found that after being thermally treated at ca. 1000 degrees C, the SiO4 tetrahedral units in the rectorite mineral are distorted, while the AlO6 octahedral units are decomposed and thus the maximum contents of active SiO2 and Al2O3 can be simultaneously achieved, and as a result, zeolite P is obtained when using the rectorite calcined at 1000 degrees C as the starting material for fabricating zeolites. Our results further revealed that like kaolin rectorite after thermal activation at a suitable temperature can be used for zeolite synthesis and thus demonstrates itself a promising feedstock for the green synthesis of zeolites directly from natural aluminosilicates without experiencing intermediate chemicals. (C) 2014 Elsevier B.V. All rights reserved.

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