skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Mesoporous aluminosilicate ropes with improved stability from protozeolitic nanoclusters

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [1];  [1];  [2]
  1. Shanghai Research Institute of Petrochemical Technology, SINOPEC, Shanghai 201208 (China)
  2. State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China)

Mesoporous aluminosilicate ropes with improved hydrothermal stability have been prepared through S{sup +}X{sup -}I{sup +} route via self-assembly of protozeolitic nanoclusters with cetyltrimethylammonium bromides (CTAB) template micelles in HNO{sub 3} solution. SEM observation confirmed that high-yield aluminosilicate ropes could be produced under proper HNO{sub 3} concentration. NO{sub 3} {sup -} ions had strong binding strength to the CTA{sup +} ions and tended to form more elongated surfactant micelles, thus fibrous products were fabricated under the direction of these long rod micelles in shearing flow. At the same time, the NO{sub 3} {sup -} ions combining with CTA{sup +} ions generated more active (CTA{sup +}NO{sub 3} {sup -}) assembly, which effectively catalysed the polymerization of protozeolitic nanoclusters with large volume into highly ordered mesostructures. Compared with normal MCM-41 silica synthesized through S{sup +}X{sup -}I{sup +} route in acidic media, the hydrothermal stability was improved considerably. These protozeolitic nanoclusters survived strongly acidic media and entered into mesostructured framework, which contributed to the improvement of hydrothermal stability. - Graphical abstract: Mesoporous aluminosilicate ropes with enhanced hydrothermal stability were fabricated from protozeolitic nanoclusters through S{sup +}X{sup -}I{sup +} route in HNO{sub 3} solution under the direction of CTAB templates.

OSTI ID:
21015684
Journal Information:
Journal of Solid State Chemistry, Vol. 180, Issue 2; Other Information: DOI: 10.1016/j.jssc.2006.11.017; PII: S0022-4596(06)00598-6; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0022-4596
Country of Publication:
United States
Language:
English