Thermal analysis of selected illite and smectite clay minerals. Part I. Illite clay specimens

Author(s):  
C. M. Earnest
Author(s):  
J. Laurence Kulp ◽  
Jose N. Perfetti

In the past decade, differential thermal analysis has developed into a very useful mineralogical technique. The theoretical background for this method has been treated by Speil, Berkelhamer, Pask, and Da vies (1945) and has been modified by Kerr and Kulp (1948, 1949). The application of the method to the clay minerals has been carried out with considerable success by a number of workers in Europe and America. In particular, Grim and co-workers (1942, 1947, 1948) have produced a number of significant papers dealing with the thermal analysis of clays. The method has been extended to other mineral groups such as the carbonates (Faust, 1949; Beck, 1946; Kerr and Kulp, 1947; Cuthbert and Rowland, 1947; Kulp, Kent, and Kerr, 1950), phosphates (Manly, 1950), sulphates (Kulp and Adler, 1950), quartz (Faust, 1948), and the hydrous iron oxides (Kulp and Trites, 1950).


Clay Minerals ◽  
1994 ◽  
Vol 29 (1) ◽  
pp. 63-68 ◽  
Author(s):  
T. J. Primmer

AbstractMuch emphasis has been placed recently on the role of Ostwald-type processes (both ripening and the step rule) in the formation of interstratified illite-smectite clay minerals during diagenesis. Closer investigation of the relationships between illite particle thickness (as defined in terms of the fundamental particle theory) and particle chemistry show that simple Ostwald ripening is too simplistic a mechanism to describe observed changes in illite thickness and composition. In addition, available thermodynamic data on clay minerals suggest that the conventional notion of metastability associated with Ostwald's step rule is an inaccurate description of the relationship between illitic clay minerals and their macroscopic 2 : 1 phyllosilicate analogues.


2012 ◽  
Vol 11 (06) ◽  
pp. 1240034 ◽  
Author(s):  
KAZUOMI NUMATA ◽  
KIMINORI SATO ◽  
KOICHIRO FUJIMOTO

Adsorption behavior of cesium (Cs) into angstrom-scale open spaces for the saponite clay mineral is investigated by making use of positronium (Ps) annihilation spectroscopy together with thermogravimetry and differential thermal analysis (TG–DTA). Ps annihilation spectroscopy reveals two kinds of open spaces with their sizes of ~ 3 Å and ~ 10 Å, respectively, after baking at 423 K for 8 h under the vacuum condition at ~ 10-5 Torr. The large open space is found to survive for the Cs -type saponite due to less hydration of the Cs cations even after the exposure to the air for 200 h. It is thus inferred that Cs is locally adsorbed in the angstrom-scale open spaces in the saponite clay minerals.


2018 ◽  
Vol 3 (1) ◽  
pp. 54-59
Author(s):  
Is Fatimah

Clay minerals are promising modifiable material for catalysis application. Fit to green chemistry issue, green catalysis based on clay minerals modification has been designed in our research group. Metal oxide and metal complexes modification onto natural and synthetic smectite clay via pillarization and intercalation processes and its application as green catalyst have been investigated.  This paper presents the study on preparation of Ni, Zr and Pt  insertion on smectite clay structure for green conversion of citronellal to menthol via catalytic hydrogen transfer mechanism and Ru-complex modified smectite clay as novel photocatalysis application.  Effect of clay structure modification was also studied in order to investigate the  relationship between physicochemical characteristic change of material modifications and its catalytic/photo-catalytic activity. Some interesting phenomena related to the interaction of metal-clay support for their performance toward reaction kinetics and mechanism are reviewed, with emphasis on the evolution of surface properties and some factors affecting catalytic/photo-catalytic activity


Author(s):  
Anke Neumann ◽  
Michael Sander ◽  
Thomas B. Hofstetter

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