Structural Analysis of Aluminum Oxyhydroxide Aerogel by Small Angle X-Ray Scattering
- Authors: Khodan A.N.1, Kopitsa G.P.2,3, Yorov K.E.4, Baranchikov A.E.5, Ivanov V.K.5,6, Feoktystov A.7, Pipich V.7
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Affiliations:
- Frumkin Institute of Physical Chemistry and Electrochemistry
- Konstantinov Petersburg Nuclear Physics Institute
- Grebenshchikov Institute of Silicate Chemistry
- Moscow State University
- Kurnakov Institute of General and Inorganic Chemistry
- National Research Tomsk State University
- Jülich Centre for Neutron Science,
- Issue: Vol 12, No 2 (2018)
- Pages: 296-305
- Section: Article
- URL: https://journal-vniispk.ru/1027-4510/article/view/195140
- DOI: https://doi.org/10.1134/S102745101802026X
- ID: 195140
Cite item
Abstract
The work presents studies on the microstructure and mesostructure of nanostructured aluminum oxyhydroxide formed as a high porous monolithic material through the surface oxidation of aluminum liquidmetal solution in mercury in a temperature- and humidity-controlled air atmosphere. The methods of X-ray diffraction analysis, thermal analysis, the low temperature adsorption of nitrogen vapors, transmission electron microscopy, small-angle and very small-angle neutron scattering, and small-angle X-ray scattering are used for comprehensive investigation of the samples synthesized at 25°С as well as that annealed at temperatures up to 1150°C. It is found that the structure of the monolithic samples can be described within the framework of a three-level model involving primary heterogeneities (typical length scale of rc ≈ 9–19 Å), forming fibrils (cross-sectional radius R ≈ 36–43 Å and length L ≈ 3200–3300 Å) or lamellae (thickness T ≈ 110 Å and width W ≈ 3050 Å) which, in turn, are integrated into large-scale aggregates (typical size Rc ≈ 1.25–1.4 μm) with an insignificant surface roughness. It is shown that a high specific surface (~200 m2/g) typical for the initial sample is maintained upon its thermal annealing up to 900°С, and it decreases to 100 m2/g after heat treatment at 1150°С due to fibrillary agglomeration.
About the authors
A. N. Khodan
Frumkin Institute of Physical Chemistry and Electrochemistry
Author for correspondence.
Email: anatole.khodan@gmail.com
Russian Federation, Moscow, 119071
G. P. Kopitsa
Konstantinov Petersburg Nuclear Physics Institute; Grebenshchikov Institute of Silicate Chemistry
Email: anatole.khodan@gmail.com
Russian Federation, Gatchina, 188300; St.-Petersburg, 199034
Kh. E. Yorov
Moscow State University
Email: anatole.khodan@gmail.com
Russian Federation, Moscow, 119991
A. E. Baranchikov
Kurnakov Institute of General and Inorganic Chemistry
Email: anatole.khodan@gmail.com
Russian Federation, Moscow, 119071
V. K. Ivanov
Kurnakov Institute of General and Inorganic Chemistry; National Research Tomsk State University
Email: anatole.khodan@gmail.com
Russian Federation, Moscow, 119071; Tomsk, 634050
A. Feoktystov
Jülich Centre for Neutron Science,
Email: anatole.khodan@gmail.com
Germany, Garching
V. Pipich
Jülich Centre for Neutron Science,
Email: anatole.khodan@gmail.com
Germany, Garching
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