Microcalorimetric studies of S/L interfacial layers: thermodynamic parameters of the adsorption of butanol-water on hydrophobized clay minerals

Microstructure, thermal expansion, hardness and thermodynamic parameters of cordierite materials synthesized from Algerian natural clay minerals and magnesia

Boletín de la Sociedad Española de Cerámica y Vidrio ◽

10.1016/j.bsecv.2020.03.008 ◽

2020 ◽

Cited By ~ 1

Author(s):

Smail Lamara ◽

Djaida Redaoui ◽

Foudil Sahnoune ◽

Menad Heraiz ◽

Nouari Saheb

Keyword(s):

Thermal Expansion ◽

Thermodynamic Parameters ◽

Clay Minerals ◽

Natural Clay

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Models of Thermodynamic Properties of Prominences

International Astronomical Union Colloquium ◽

10.1017/s0252921100065799 ◽

1979 ◽

Vol 44 ◽

pp. 349-355

Author(s):

R.W. Milkey

Keyword(s):

Thermodynamic Properties ◽

Mass Transport ◽

Emission Spectrum ◽

Thermodynamic Parameters ◽

Working Group ◽

Physical Processes ◽

Theoretical Concepts ◽

Group 3 ◽

Observational Techniques

The focus of discussion in Working Group 3 was on the Thermodynamic Properties as determined spectroscopically, including the observational techniques and the theoretical modeling of physical processes responsible for the emission spectrum. Recent advances in observational techniques and theoretical concepts make this discussion particularly timely. It is wise to remember that the determination of thermodynamic parameters is not an end in itself and that these are interesting chiefly for what they can tell us about the energetics and mass transport in prominences.

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Hydrated form of some clay minerals observed using a film sealed environmental cell

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100107502 ◽

1978 ◽

Vol 36 (1) ◽

pp. 72-73

Author(s):

N. Kohyama ◽

K. Fukushima ◽

A. Fukami

Keyword(s):

Clay Minerals ◽

Morphological Changes ◽

Carbon Film ◽

Electron Microscopic Observation ◽

Adsorbed Water ◽

Electron Microscopic ◽

Hydrated Form ◽

Thin Carbon ◽

Environmental Cell ◽

Thin Carbon Film

Since the interlayer or adsorbed water of some clay minerals are quite easily dehydrated in dried air, in vacuum, or at moderate temperatures even in the atmosphere, the hydrated forms have not been observed by a conventional electron microscope(TEM). Recently, specific specimen chambers, “environmental cells(E.C.),” have been developed and confirmed to be effective for electron microscopic observation of wet specimen without dehydration. we observed hydrated forms of some clay minerals and their morphological changes by dehydration using a TEM equipped with an E.C..The E.C., equipped with a single hole copper-microgrid sealed by thin carbon-film, attaches to a TEM(JEM 7A) with an accelerating voltage 100KV and both gas pressure (from 760 Torr to vacuum) and relative humidity can be controlled. The samples collected from various localities in Japan were; tubular halloysite (l0Å) from Gumma Prefecture, sperical halloysite (l0Å) from Tochigi Pref., and intermediate halloysite containing both tubular and spherical types from Fukushima Pref..

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The morphologies and electrical properties of indium contacts on (100) cadmium telluride surfaces

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100131747 ◽

1992 ◽

Vol 50 (2) ◽

pp. 1422-1423

Author(s):

A.M. Letsoalo ◽

M.E. Lee ◽

E.O. de Neijs

Keyword(s):

Electrical Properties ◽

Cadmium Telluride ◽

Methanol Solution ◽

Electrical Characteristics ◽

Metal Contacts ◽

Deposition Technique ◽

Interfacial Layers ◽

Semiconductor Contacts ◽

Grown Single Crystal ◽

Diamond Abrasive

Semiconductor devices require metal contacts for efficient collection of electrical charge. The physics of these metal/semiconductor contacts assumes perfect, abrupt and continuous interfaces between the layers. However, in practice these layers are neither continuous nor abrupt due to poor nucleation conditions and the formation of interfacial layers. The effects of layer thickness, deposition rate and substrate stoichiometry have been previously reported. In this work we will compare the effects of a single deposition technique and multiple depositions on the morphology of indium layers grown on (100) CdTe substrates. The electrical characteristics and specific resistivities of the indium contacts were measured, and their relationships with indium layer morphologies were established.Semi-insulating (100) CdTe samples were cut from Bridgman grown single crystal ingots. The surface of the as-cut slices were mechanically polished using 5μm, 3μm, 1μm and 0,25μm diamond abrasive respectively. This was followed by two minutes immersion in a 5% bromine-methanol solution.

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Colloidal systems in soils

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100168050 ◽

1994 ◽

Vol 52 ◽

pp. 64-65

Author(s):

J. Thieme ◽

J. Niemeyer ◽

P. Guttman

Keyword(s):

Clay Minerals ◽

Polymeric Materials ◽

Spatial Arrangement ◽

High Specific Surface Area ◽

Turnover Rates ◽

Colloidal Systems ◽

Chemical Conditions ◽

Aggregation Phenomena ◽

Iron And Manganese ◽

Soil Colloids

In soil science the fraction of colloids in soils is understood as particles with diameters smaller than 2μm. Clay minerals, aquoxides of iron and manganese, humic substances, and other polymeric materials are found in this fraction. The spatial arrangement (microstructure) is controlled by the substantial structure of the colloids, by the chemical composition of the soil solution, and by thesoil biota. This microstructure determines among other things the diffusive mass flow within the soils and as a result the availability of substances for chemical and microbiological reactions. The turnover of nutrients, the adsorption of toxicants and the weathering of soil clay minerals are examples of these surface mediated reactions. Due to their high specific surface area, the soil colloids are the most reactive species in this respect. Under the chemical conditions in soils, these minerals are associated in larger aggregates. The accessibility of reactive sites for these reactions on the surface of the colloids is reduced by this aggregation. To determine the turnover rates of chemicals within these aggregates it is highly desirable to visualize directly these aggregation phenomena.

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