The kinetic analysis of formation behavior for the MgB2 phase

2007 ◽  
Vol 443 (1-2) ◽  
pp. 161-165 ◽  
Author(s):  
Shicheng Yan ◽  
Yafeng Lu ◽  
Guoqing Liu ◽  
Guo Yan ◽  
Lian Zhou
ChemInform ◽  
2007 ◽  
Vol 38 (38) ◽  
Author(s):  
Shicheng Yan ◽  
Yafeng Lu ◽  
Guoqing Liu ◽  
Guo Yan ◽  
Lian Zhou

2007 ◽  
Vol 546-549 ◽  
pp. 2035-2039 ◽  
Author(s):  
S.C. Yan ◽  
G. Yan ◽  
Ya Feng Lu ◽  
Y. Feng ◽  
Lian Zhou

Bulk samples with the stoichiometry of Mg:B=1:2 and 1:4 were prepared by solid state reaction method. The microstructure and constituent of the samples were investigated by using the scanning electron microscope (SEM) and the x-ray diffraction (XRD). XRD results showed that the MgB2 phase was first formed in all the samples with different stoichiometry of Mg and B, which indicated that the MgB2 was the most thermodynamically stable phase in the Mg-B binary system. For the samples of Mg:B=1:2, the MgB2 single phase was formed very well when these samples were sintered at 650°C~700°C. For the samples with later added Mg reaching to the stoichiometry of Mg:B=1:2, a longer reaction time or higher reaction temperature was required for the formation of the MgB2 single phase. The SEM results showed that the samples with later added Mg had dense microstructures, suggesting that the later addition of Mg could reduce the porosity of the sample. A small increase of the superconducting transition temperature, Tc, in the Mg addition sample resulted from the dense microstructures.


1965 ◽  
Vol 13 (01) ◽  
pp. 155-175 ◽  
Author(s):  
H. C Hemker ◽  
P.W Hemker ◽  
E. A Loeliger

SummaryApplication of the methods of enzyme-kinetic analysis to the results of clotting tests is feasible and can yield useful results. However, the standard methods of enzyme kinetics are not applicable without modifications imposed by the peculiarities of the blood-clotting enzyme system. The influence of the following complicating circumstances is calculated :1. Substrate is not present in excess.2. Only relative measures exist for concentrations of substrate or enzymes.3. Enzymes and substrates are often added together.4. Reagents are not pure.5. Clotting-time is our only measure for clotting-velocity.Formulas are deduced, which makes it possible to recognize the effect of these complications.


2013 ◽  
Vol 51 (11) ◽  
pp. 807-812
Author(s):  
EunHye Jung ◽  
Bong-Yong Jeong
Keyword(s):  

1995 ◽  
Vol 32 (4) ◽  
pp. 225-231 ◽  
Author(s):  
Toru HARIGAI ◽  
Shinya KIMURA ◽  
Shuichi KAKURAI
Keyword(s):  

2018 ◽  
Author(s):  
yongson hong ◽  
Kye-Ryong Sin ◽  
Jong-Su Pak ◽  
Chol-Min Pak

<p><b>In this paper, the deficiencies and cause of previous adsorption kinetic models were revealed, new adsorption rate equation has been proposed and its validities were verified by kinetic analysis of various experimental data.</b> <b>This work is a new view on the adsorption kinetics rather than a comment on the previous adsorption papers.</b></p>


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