Entropy of mixing as a stabilization factor of the cubic phase of Scandium doped zirconia

2019 ◽  
Vol 333 ◽  
pp. 16-17
Author(s):  
Gene Whyman ◽  
Alexander Kalashnikov ◽  
Michael Zinigrad
Author(s):  
Steven D. Toteda

Zirconia oxygen sensors, in such applications as power plants and automobiles, generally utilize platinum electrodes for the catalytic reaction of dissociating O2 at the surface. The microstructure of the platinum electrode defines the resulting electrical response. The electrode must be porous enough to allow the oxygen to reach the zirconia surface while still remaining electrically continuous. At low sintering temperatures, the platinum is highly porous and fine grained. The platinum particles sinter together as the firing temperatures are increased. As the sintering temperatures are raised even further, the surface of the platinum begins to facet with lower energy surfaces. These microstructural changes can be seen in Figures 1 and 2, but the goal of the work is to characterize the microstructure by its fractal dimension and then relate the fractal dimension to the electrical response. The sensors were fabricated from zirconia powder stabilized in the cubic phase with 8 mol% percent yttria. Each substrate was sintered for 14 hours at 1200°C. The resulting zirconia pellets, 13mm in diameter and 2mm in thickness, were roughly 97 to 98 percent of theoretical density. The Engelhard #6082 platinum paste was applied to the zirconia disks after they were mechanically polished ( diamond). The electrodes were then sintered at temperatures ranging from 600°C to 1000°C. Each sensor was tested to determine the impedance response from 1Hz to 5,000Hz. These frequencies correspond to the electrode at the test temperature of 600°C.


Author(s):  
David M. Anderson ◽  
Tomas Landh

First discovered in surfactant-water liquid crystalline systems, so-called ‘bicontinuous cubic phases’ have the property that hydropnilic and lipophilic microdomains form interpenetrating networks conforming to cubic lattices on the scale of nanometers. Later these same structures were found in star diblock copolymers, where the simultaneous continuity of elastomeric and glassy domains gives rise to unique physical properties. Today it is well-established that the symmetry and topology of such a morphology are accurately described by one of several triply-periodic minimal surfaces, and that the interface between hydrophilic and hydrophobic, or immiscible polymer, domains is described by a triply-periodic surface of constant, nonzero mean curvature. One example of such a dividing surface is shown in figure 5.The study of these structures has become of increasing importance in the past five years for two reasons:1)Bicontinuous cubic phase liquid crystals are now being polymerized to create microporous materials with monodispersed pores and readily functionalizable porewalls; figure 3 shows a TEM from a polymerized surfactant / methylmethacrylate / water cubic phase; and2)Compelling evidence has been found that these same morphologies describe biomembrane systems in a wide range of cells.


Author(s):  
E.K. Goo ◽  
R.K. Mishra

Ferroelectric domains are twins that are formed when PZT undergoes a phase transformation from a non-ferroelectric cubic phase to a ferroelectric tetragonal phase upon cooling below ∼375°C.,1 The tetragonal phase is spontaneously polarized in the direction of c-axis, making each twin a ferroelectric domain. Thin foils of polycrystalline Pb (Zr.52Ti.48)03 were made by ion milling and observed in the Philips EM301 with a double tilt stage.


1983 ◽  
Vol 50 (02) ◽  
pp. 563-566 ◽  
Author(s):  
P Hellstern ◽  
K Schilz ◽  
G von Blohn ◽  
E Wenzel

SummaryAn assay for rapid factor XIII activity measurement has been developed based on the determination of the ammonium released during fibrin stabilization. Factor XIII was activated by thrombin and calcium. Ammonium was measured by an ammonium-sensitive electrode. It was demonstrated that the assay procedure yields accurate and precise results and that factor XIII-catalyzed fibrin stabilization can be measured kinetically. The amount of ammonium released during the first 90 min of fibrin stabilization was found to be 7.8 ± 0.5 moles per mole fibrinogen, which is in agreement with the findings of other authors. In 15 normal subjects and in 15 patients suffering from diseases with suspected factor XIII deficiency there was a satisfactory correlation between the results obtained by the “ammonium-release-method”, Bohn’s method, and the immunological assay (r1 = 0.65; r2= 0.70; p<0.01). In 3 of 5 patients with paraproteinemias the values of factor XIII activity determined by the ammonium-release method were markedly lower than those estimated by the other methods. It could be shown that inhibitor mechanisms were responsible for these discrepancies.


2020 ◽  
Vol 10 ◽  
Author(s):  
Manish Dwivedi ◽  
Vijay Tripathi ◽  
Dhruv Kumar ◽  
Dwijendra K. Gupta

Aims: CdS nanoparticles are an attractive material having application in various field like as pigment in paints, biotag for bioimaging and many more optoelectronic as well as biological applications. Present study aims to synthesize and characterize the CdS nanoparticles to make it applicable in different areas Objectives: Preparation CdS nanoparticles by using simple and facile chemical methods and further physical and structural characterization using various physical tools Methods: In present work CdS nanoparticles has been synthesized by using rationally simple chemical precipitation method with some modi-fication on temperature and incubation time in existed methods. Characterizations were done by employing XRD, SEM, TEM, AFM tech-niques Results: Simple chemical method produces the CdS nanoparticles with the size about 100-200 nm in length and 5-10 nm in diameter. The SEM studies show that the CdS nanoparticles can agglomerate and form a continuous network like structure. The X-ray diffraction (XRD) measurements show the single-phase formation of CdS nanoparticles with the structure of cubic phase, and the broadening of XRD patterns indicates that the prepared samples are nanostructured. Our analysis on CdS nanoparticles by using transmission electron microscope and atomic force microscope (AFM) revealed that the nanoparticles form both spherical and nearly rod shaped with the average size applicable for biotagging. UV-Vis spectroscopic analysis reveals blue shift in the absorption peak probably caused by quantum confinement Conclusion: The observed CdS nanoparticles were appeared yellow in color. The XRD pattern of the CdS nanoparticles showed that the materials were of nanometric sized regime with a predominantly cubic phase along with the rod and round morphology. The study and char-acterization of CdS nanoparticles will bring us a new approach to understand biological problem by tagging nanoparticles with biomolecules and further suggests that the CdS nanoparticles formulate it more suitable biocompatible nanomaterial for biotagging and bioimaging


Author(s):  
A. M. Savchenko ◽  
Yu. V. Konovalov ◽  
A. V. Laushkin

The relationship of the first and second laws of thermodynamics based on their energy nature is considered. It is noted that the processes described by the second law of thermodynamics often take place hidden within the system, which makes it difficult to detect them. Nevertheless, even with ideal mixing, an increase in the internal energy of the system occurs, numerically equal to an increase in free energy. The largest contribution to the change in the value of free energy is made by the entropy of mixing, which has energy significance. The entropy of mixing can do the job, which is confirmed in particular by osmotic processes.


1996 ◽  
Vol 61 (6) ◽  
pp. 837-843
Author(s):  
Ladislav Kosa ◽  
Ivan Nerád ◽  
Katarína Adamkovičová ◽  
Jozef Strečko ◽  
Ivo Proks

Activities of the components, the Gibbs energy of mixing, and the excess entropy of mixing have been calculated for the Ca2MgSi2O7-CaSiO3 system. The mole fractions of the components were calculated assuming that in the point of the formal component Ca2MgSi2O7, the molar mass of the quasi-real particle in the melt corresponds to its formula molar mass, whereas in the point of the formal component CaSiO3 the molar mass of the quasi-real particle in the melt is 8.5 times higher than as corresponds to its formula. The fact that the enthalpy of mixing is zero whereas the excess entropy of mixing is non-zero suggests that Ca2MgSi2O7-CaSiO3 melts behave as athermal solutions.


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