Equilibrium Phase Diagrams for Analysis of the Oxidation of III-V Compound Semiconductors

1989 ◽  
Vol 148 ◽  
Author(s):  
G. P. Schwartz

ABSTRACTThe phases which result from the oxidation of III-V compound semiconductors can be predicted from a knowledge of the condensed phase portion of their equilibrium phase diagrams. Examples will be shown for arsenides, antimonides, and phosphides. Use of these diagrams explicitly presumes equilibrium growth conditions, and that assumption often fails. In such cases kinetic rather than thermodynamic factors dominate the determination of the observed phases. Examples of this phenomenon for anodic oxidation will be presented. Recent interest in high pressure oxidation conditions as a means of alleviating kinetic limitations will be discussed for InP. The phase diagrams can also be used to predict interfacial reactions under certain conditions and data for GaAs will serve to illustrate this point.

1980 ◽  
Vol 102 (3) ◽  
pp. 633-640
Author(s):  
K. C. Rolle ◽  
J. N. Crisp ◽  
A. N. Palazotto

In the determination of equilibrium phase diagrams, i.e., pressure volume-temperature relations for lubricants at pressures up to 2800 MPa and temperatures of 378K, one must carry out a highly sophisticated design of a high pressure apparatus. In 1935 Bridgman designed a piston-displacement device and measured the compressibility of numerous materials at high pressures. However, in order to obtain accurate equilibrium phase diagrams for lubricants, Bridgman’s relatively crude analysis must be considerably refined. The authors have extended this original design using finite element techniques to accurately correct pertinent measurements which are in turn incorporated into the expressions used in determining the pressure-volume temperature relations of lubricants.


1980 ◽  
Vol 35 (4) ◽  
pp. 381-388 ◽  
Author(s):  
W. Weppner ◽  
Chen Li-chuan ◽  
W. Piekarczyk

Abstract The coulometric titration technique is extended to treat general cases of systems of any number of components. Complete equilibrium phase diagrams and thermodynamic properties are obtained from readily and precisely measurable electrical quantities, employing only a small number of samples. General equations are derived which directly relate the cell voltage to the standard Gibbs energies, enthalpies and entropies of formation of all phases involved without the necessity of considering specific cell reactions. The application of the technique to the ternary system Cu-Ge-O is demonstrated.


AIChE Journal ◽  
2007 ◽  
Vol 53 (6) ◽  
pp. 1608-1619 ◽  
Author(s):  
Sau M. Lai ◽  
Mai Y. Yuen ◽  
Leo K. S. Siu ◽  
Ka M. Ng ◽  
Christianto Wibowo

1992 ◽  
Vol 187 (1) ◽  
pp. 137-143 ◽  
Author(s):  
Lizhu Song ◽  
Hua Yang ◽  
Muyu Zhao ◽  
Zhongyi Shen ◽  
Yong Liu

2019 ◽  
Vol 64 (8) ◽  
pp. 848-858
Author(s):  
K. D. Litasov ◽  
D. D. Badyukov

In the paper we present results of studies of thick shock melt veins in NWA 5011 L6 chondrite. The veins contain a wide variety of high-pressure phases that correspond to contrast values of pressure-temperature parameters on equilibrium phase diagrams. Olivine was transformed to ringwoodite and wadsleyte, orthopyroxene to majorite, akimotoite, and bridgmanite glass, maskelenite is converted to jadeite (+SiO2) and lingunite, apatite to tuite, and chromite to the phase with the calcium ferrite (mCF-FeCr2O4) structure. ) The peak PT shock parameters for NWA 5011 seem highest among the ones for other shocked chondrites according to wide occurrence of lingunite and bridgmanite glass and are considerable higher than 25 GPa and 2500 K. Akimotoite crystals in a quenched matrix of shock melt veins were found for the first time. Probably, they initially crystallized as bridgmanite, since akimotoite is not a liquidus phase in related systems. Plagioclase-chromite aggregates have been established, which characterize the late stages of the shock process and are formed during successive crystallization from isolated pockets of the impact melt.


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