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The x-ray identification and crystal structures of clay minerals
01 Jan 1961-
About: The article was published on 1961-01-01 and is currently open access. It has received 966 citations till now. The article focuses on the topics: Clay minerals.
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TL;DR: In this paper, the infrared spectra of synthetic kaolinites, with various degrees of substitution of hydroxyls by OD groups, were used to identify the stretching bands due to inner surface hydroxys of kaolinite.
Abstract: Examination of the infrared spectra of synthetic kaolinites, with various degrees of substitution of hydroxyls by OD groups, allows a more detailed attribution of the stretching bands due to inner-surface hydroxyls of kaolinite. Among the three innersurface OH groups of the unit cell, two are nearly perpendicular to the sheet and give coupled vibrations which are responsible for the bands around 3695 and 3670 cm−1; the band near 3655 cm−1 is due to the other hydroxyl, which is lying close to the sheet.
87 citations
TL;DR: In this article, an expert system was proposed to accurately describe the defect structure of kaolinites based on a few measurements taken from a normal powder diffraction profile, which was verified for nine kaolinite samples for which the defect structures was previously determined by comparison of calculated and observed diffraction profiles.
Abstract: Until recently, the determination of the defect structures (previously referred to incorrectly as “crystallinity”) of kaolinites has been obtained in one of two ways: (1) measurement of the Hinckley index, or (2) by comparing calculated X-ray diffraction patterns based on a model of the defect structure (including types of defects and abundances) with experimental diffraction profiles. The Hinckley method is simple and easy to perform but contains no real information about the defect structure. Calculated XRD patterns are based on real defects but these calculations are time consuming and require some skill in application. Another approach is proposed: an expert system which will accurately describe the defect structure of kaolinites based on a few measurements taken from a normal powder diffraction profile. This system has been verified for nine kaolinite samples for which the defect structure was previously determined by comparison of calculated and observed diffraction profiles. The expert system reproduced the correct defect structure for each of the samples.
85 citations
TL;DR: In this article, the structural transformation of dioctahedral 2:1 layer silicates (illite, montmorillonite, glauconite and celadonite) during a dehydoxylation-rehydroxylation process has been studied by X-ray diffraction, thermal analysis, and infrared spectroscopy.
Abstract: The structural transformation of dioctahedral 2:1 layer silicates (illite, montmorillonite, glauconite, and celadonite) during a dehydoxylation-rehydroxylation process has been studied by X-ray diffraction, thermal analysis, and infrared spectroscopy. The layers of the samples differ in the distribution of the octahedral cations over the cis- and trans-sites as determined by the analysis of the positions and intensities of the 11l, 02l reflections, and that of the relative displacements of adjacent layers along the a axis (c cos s/a), as well as by dehydroxylation-temperature values. One illite, glauconite, and celadonite consist of trans-vacant (tv) layers; Wyoming montmorillonite is composed of cis-vacant (cv) layers, whereas in the other illite sample tv and cv layers are interstratified. The results obtained show that the rehydroxylated Al-rich minerals (montmorillonite, illites) consist of tv layers whatever the distribution of octahedral cations over cis- and trans-sites in the original structure. The reason for this is that in the dehydroxylated state, both tv and cv layers are transformed into the same layer structure where the former trans-sites are vacant. The dehydroxylation of glauconite and celadonite is accompanied by a migration of the octahedral cations from former cis-octahedra to empty trans-sites. The structural transformation of these minerals during rehydroxylation depends probably on their cation composition. The rehydroxylation of celadonite preserves the octahedral-cation distribution formed after dehydroxylation. Therefore, most 2:1 layers of celadonite that rehydroxylate (~75%) have cis-vacant octahedra and, only in a minor part of the layers, a reverse cation migration from former trans-sites to empty octahedra occurred. In contrast, for a glauconite sample with a high content in IVAl and VIAl the rehydroxylation is accompanied by the reverse cation migration and most of the 2:1 layers are transformed into tv layers.
85 citations
TL;DR: Colloidal dispersions produced from the swollen crystals of vermiculite minerals are morphologically unique and show strong filmforming characteristics.
Abstract: Chemical treatments involving ion exchange cause gross onedimensional swelling in water of single crystals of vermiculite minerals. A delicate balance of forces holds the individual silicate layers (10 angstroms thick) parallel to one another although separated by several hundred angstroms. Colloidal dispersions produced from the swollen crystals are morphologically unique and show strong filmforming characteristics.
84 citations
TL;DR: In the course of the studies on soil allophane, it was noticed that certain Ando soils contained two different mineral colloids together, in addition to crystalline clay minerals and free sesquioxides as mentioned in this paper.
Abstract: Allophane has been known to occur widely in volcanic ash soils in Japan and New Zealand. However, exact knowledge of its nature has not been well established, mainly because of extreme difficulty to separate it in pure state and of its x-amorphous nature. In the course of the studies on soil allophane, it was noticed that certain Ando soils contained two different mineral colloids together, in addition to crystalline clay minerals and free sesquioxides. X-ray examination revealed that one was x-amorphous colloid which would be called allophane, and the other an unknown colloid of low crystallinity. Imogolite*** was proposed as the name of the latter colloid by the present authors after imogo in which imogolite was first found. Imogo is a brownish yellow, volcanic ash soil. in the Kuma basin in the Kumamoto Prefecture3). When deferration treatment is applied to the soils, allophane disperses both in an acid and alkaline media, whereas imogolite disperses in an acid medium and flocculates in an alk...
84 citations