On controlled solidification studies of some TiO2 binary alloys

1992 ◽  
Vol 7 (4) ◽  
pp. 980-991 ◽  
Author(s):  
C.T. Yen ◽  
D.O. Nason ◽  
W.A. Tiller

TiO2 single crystal fibers in the 1 mm diameter range were pulled from different alloy melts using the laser heated pedestal melting technique. The alloying elements studied were CaO, MnO, MgO, SiO2, FeO, and Al2O3. Phase diagram solute partition coefficient, k0, maximum solid solubility limit, CS(max), eutectic concentration, CE, and eutectic temperature, TE, were determined for each of these alloys. Solute redistribution effects in the solid, controlled precipitation in the solid, smooth solid-liquid interfaces in the presence of high melt concentrations and substantial crystal broadening by fluid migration up the solid from the melt all indicated the existence of a very strong thermodynamic field and a large solid diffusion coefficient operating in the solid behind the solid/liquid interface.

Author(s):  
Vasile Bratu ◽  
Ileana Nicoleta Popescu

Abstract In order to determine the optimum geometry of the ingot mold format (the format of ingot mold with a diameter per height ratio H / D <3 and the conicity of minimum 7%) was analyzed by mathematical modeling of solidification and segregation of the carbon and sulfur in it.It was considered 205Cr115 steel type (according with , STAS 3611 - Romanian stardandization) and known also as X210Cr12 steel type (according with European standard). It has been considered an element of volume of coordinates x, y, z in the solidifying ingot and have made the following assumptions: (i) the equilibrium distribution ratio K, is applied to the solid-liquid interface; (ii) solid diffusion is negligible during solidification; and (iii) the solid density is constant during solidification. In carrying out the simulation of segregation mechanisms are resolved heat transfer equation, that simulating the solidification process and are are solved the interdendritic fluid equation of motion.


1990 ◽  
Vol 43 (5S) ◽  
pp. S56-S58 ◽  
Author(s):  
K. Brattkus

We adapt the recent derivation of a long-wave evolution equation for a solid-liquid interface undergoing directional solidification near the limit of absolute stability to the case of a symmetric model that includes solid diffusion. The stability of steady and spatially periodic solutions are investigated and it is found that these cellular solutions are subject to an oscillatory instability with twice the wavenumber of the underlying pattern. We discuss this instability in the context of experiments on the directional solidification of nematic liquid crystals.


Author(s):  
J.A. Panitz

The first few atomic layers of a solid can form a barrier between its interior and an often hostile environment. Although adsorption at the vacuum-solid interface has been studied in great detail, little is known about adsorption at the liquid-solid interface. Adsorption at a liquid-solid interface is of intrinsic interest, and is of technological importance because it provides a way to coat a surface with monolayer or multilayer structures. A pinhole free monolayer (with a reasonable dielectric constant) could lead to the development of nanoscale capacitors with unique characteristics and lithographic resists that surpass the resolution of their conventional counterparts. Chemically selective adsorption is of particular interest because it can be used to passivate a surface from external modification or change the wear and the lubrication properties of a surface to reflect new and useful properties. Immunochemical adsorption could be used to fabricate novel molecular electronic devices or to construct small, “smart”, unobtrusive sensors with the potential to detect a wide variety of preselected species at the molecular level. These might include a particular carcinogen in the environment, a specific type of explosive, a chemical agent, a virus, or even a tumor in the human body.


1999 ◽  
Vol 39 (7) ◽  
pp. 91-98 ◽  
Author(s):  
Ryan N. Jordan ◽  
Eric P. Nichols ◽  
Alfred B. Cunningham

Bioavailability is herein defined as the accessibility of a substrate by a microorganism. Further, bioavailability is governed by (1) the substrate concentration that the cell membrane “sees,” (i.e., the “directly bioavailable” pool) as well as (2) the rate of mass transfer from potentially bioavailable (e.g., nonaqueous) phases to the directly bioavailable (e.g., aqueous) phase. Mechanisms by which sorbed (bio)surfactants influence these two processes are discussed. We propose the hypothesis that the sorption of (bio)surfactants at the solid-liquid interface is partially responsible for the increased bioavailability of surface-bound nutrients, and offer this as a basis for suggesting the development of engineered in-situ bioremediation technologies that take advantage of low (bio)surfactant concentrations. In addition, other industrial systems where bioavailability phenomena should be considered are addressed.


2020 ◽  
Vol 124 (5) ◽  
pp. 2987-2993
Author(s):  
Chi-Kuang Sun ◽  
Yi-Ting Yao ◽  
Chih-Chiang Shen ◽  
Mu-Han Ho ◽  
Tien-Chang Lu ◽  
...  

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