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Phase transformations in xerogels of mullite compositionMonophasic and diphasic xerogels have been prepared as precursors for mullite (3Al2O3-2SiO2). Monophasic xerogel was synthesized from tetraethyl orthosilicate and aluminum nitrate nanohydrate and the diphasic xerogel from colloidal suspension of silica and boehmite. The chemical and structural evolutions, as a function of thermal treatment, in these two types of sol-gel derived mullite precursor powders have been characterized by DTA, TGA, X-ray diffraction, SEM and infrared spectroscopy. Monophasic xerogel transforms to an Al-Si spinel from an amorphous structure at approximately 980 C. The spinel then changes into mullite on further heating. Diphasic xerogel forms mullite at approximately 1360 C. The components of the diphasic powder react independently up to the point of mullite formation. The transformation in the monophasic powder occurs rapidly and yields strongly crystalline mullite with no other phases present. The diphasic powder, however, transforms rather slowly and contains remnants of the starting materials (alpha-Al2O3, cristobalite) even after heating at high temperatures for long times (1600 C, 6 hr). The diphasic powder could be sintered to high density but not the monophasic powder in spite of its molecular level homogeneity.
Document ID
19890001667
Acquisition Source
Legacy CDMS
Document Type
Technical Memorandum (TM)
Authors
Hyatt, Mark J.
(NASA Lewis Research Center Cleveland, OH., United States)
Bansal, Narottam P.
(Case Western Reserve Univ. Cleveland, Ohio., United States)
Date Acquired
September 5, 2013
Publication Date
January 1, 1988
Subject Category
Nonmetallic Materials
Report/Patent Number
NASA-TM-101349
NAS 1.15:101349
E-4332
Report Number: NASA-TM-101349
Report Number: NAS 1.15:101349
Report Number: E-4332
Accession Number
89N11038
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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