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Journal ArticleDOI

Reference Chlorite Characterization for Chlorite Identification in Soil Clays

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TLDR
In this article, the effect of particle size on DTA, X-ray diffraction, glycol retention, and cation exchange capacity for eleven chlorite samples of clinochlore, prochlorite, thuringite, corundophilite, and leuchtenbergite are given.
Abstract
Literature pertaining to differential thermal and X-ray diffraction of chlorite minerals is reviewed. Optical, DTA, and X-ray data for eleven chlorite samples of clinochlore, prochlorite, thuringite, corundophilite, and leuchtenbergite are given. The effect of particle size (105 to −1 μ) on DTA, X-ray diffraction, glycol retention, and cation exchange capacity are given for two thuringites, one clinochlore, and one prochlorite. Identification of chlorite by DTA in a soil clay containing a mixture of minerals is improbable at the present time except under very favorable circumstances. However, for relatively pure chlorite samples, variations in chemical composition are reflected in the differential thermal curves. The largest change in the thermogram is produced by ferric iron which lowers the peak temperature from 720° C to 610° C. Differences in thermal behavior between low and high ferric iron chlorite species are maintained for any given particle size. Chlorite thermograms obtained by different investigators show much greater variation than the differences in thermograms for other clay minerals determined on different equipment. X-ray diffraction can be used to positively identify chlorite in a soil clay, (a) by careful analysis of reflections at least as great as 14 A, and (b) by the influence heat treatment (550° C for 30 minutes) has on the X-ray pattern. Heat treatment produces marked changes in the X-ray pattern of the finer particle size samples and the magnitude of the change effected is greater for high iron chlorites (thuringite) than for low iron chlorites (clinochlore and prochlorite). Olivine is not the recrystallization product for thuringite. The smallest size fractions show no tendency toward vermiculite or montmorillonoid. Cation exchange capacity for silt size chlorites varies from 4 to 32 m.e./100gm., and for −2 μ chlorite particles from 30 to 47 m.e./100gm. Cation exchange capacities for −2 μ and −1 μ chlorites are essentially the same. Ethylene glycol retention increases with decreasing particle size. Glycol retention for −2 μ chlorite samples varies from 25 to 40 mg, glycol/gm, clay. For −1 μ chlorite material, glycol retention is 2 to 4 times greater than for −2 μ material.

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Citations
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Journal ArticleDOI

Differential Settling Tendencies of Clay Minerals in Saline Waters1

TL;DR: In this article, the authors used pipette analysis, Oden balance techniques, Kelley-Wiegner manometer methods, and spectrophotometric methods, using artificial sea-water and filtered Gulf of Mexico water.
Journal ArticleDOI

Experimental investigation of the thermal and mechanical stability of rocks for high-temperature thermal-energy storage

TL;DR: In this paper, six types of rocks of Alpine origin were investigated for their suitability for high-temperature packed-bed thermal energy storage, and they were thermally cycled in laboratory furnaces between about 100 °C and 600 °C with a heating rate of 2.6 °C /min and assessed in terms of their specific heat capacity and porosity as well as the degree of cracking, fracturing, and disintegration.
Journal ArticleDOI

Characterization of pulverized granitoids in a shallow core along the San Andreas Fault, Littlerock, CA

TL;DR: In this paper, the authors present results on the composition, structure and particle size distribution (PSD) of pulverized and damaged granitic rocks in a 42m-deep core adjacent to the San Andreas Fault near Littlerock, CA.
Journal ArticleDOI

The chlorite series of flagstaff hill area, california: a preliminary investigation

TL;DR: The results of X-ray diffraction, DTA, and chemical tests are presented for some chlorites typical of the Flagstaff Hill area as mentioned in this paper, which is notable for the large variety of chlorite types occurring in considerable quantities.
References
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Journal ArticleDOI

Differential Thermal Analysis

M. J. Vold
- 01 Jun 1949 - 
Journal ArticleDOI

A new review of the chlorites

Max H. Hey
TL;DR: The chlorites form an extensive isostructural series with a high degree of isomorphous substitution, within which it has always been difficult to define or delimit species; until recently, owing to the lack of adequate X-ray studies, several structurally distinct species were included with the group, further complicating the problem as mentioned in this paper.
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