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Journal ArticleDOI

Energy Changes in Dehydroxylation of Silicate Minerals

TLDR
In this article, the dehydroxylation reactions of three 2: 1 layer type clay minerals, illite, vermiculite and chlorite, and the measurement of relative thermal energies involved in the process have been reported.
Abstract
The dehydroxylation reactions of three 2: 1 layer type clay minerals, illite, vermiculite and chlorite and the measurement of relative thermal energies involved in the process have been reported.

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Journal ArticleDOI

Physico-Chemical Properties of Clay Minerals from Alluvial Soil Sediment of West Bengal

TL;DR: The results indicated the presence of illite (2: mical type) as the dominant clay mineral with traces of kaolinite in alluvial soil clays (pond sediments) as mentioned in this paper.
Journal ArticleDOI

Thermal Decomposition of Vermiculites: Kinetics of Dehydration and Dehydroxylation Processes

TL;DR: In this article, the thermal decomposition reactions of homoionic clay minerals, viz. vermiculite, in air in the temperature range 30°-1000°C by thermo-analytical methods are reported.
References
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Book

Textbook of quantitative inorganic analysis

TL;DR: Textbook of quantitative inorganic analysis as discussed by the authors, Textbook of qualitative and quantitative analysis of inorganic properties, textbook of quantitatively analytically-inorganic analysis, as discussed by the authors.
Journal ArticleDOI

Homogeneous and Inhomogeneous Mechanisms in the Dehydroxylation of Minerals

H. F. W. Taylor
- 01 Jan 1962 - 
TL;DR: In this paper, a new approach to the dehydroxylation of clay minerals is suggested, based on the concept of inhomogeneous mechanisms, and it is shown that certain calcium minerals undergo dehydroxymethylation in this way.
Journal ArticleDOI

Kinetics of Clay Dehydration

P. Murray
- 01 Jan 1955 - 
TL;DR: In this paper, the first order nature of the dehydration reaction is shown to be the underlying basis of the type of curve obtained in differential thermal analysis, and the effect of heating at a constant rate on the progress of a reaction for which the isothermal velocity constants are known.
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