Thermodynamics and kinetics of room-temperature microstructural evolution in copper films

2003 ◽  
Vol 94 (5) ◽  
pp. 2874-2881 ◽  
Author(s):  
C. Detavernier ◽  
S. Rossnagel ◽  
C. Noyan ◽  
S. Guha ◽  
C. Cabral ◽  
...  
Keyword(s):  
Microstructural Evolution ◽  
Room Temperature ◽  
Copper Films ◽  
Thermodynamics And Kinetics ◽  
Kinetics Of

scholarly journals Microstructural Evolution, Thermodynamics and Kinetics of Mo-Tm2O3 Powder Mixtures during Ball Milling

2016 ◽  
Author(s):  
Yong Luo ◽  
Guang Ran ◽  
Nanjun Chen ◽  
Qiang Shen ◽  
Yaoli Zhang
Keyword(s):  
Solid Solution ◽  
Ball Milling ◽  
Microstructural Evolution ◽  
Driving Force ◽  
Phase Evolution ◽  
Heat Of Mixing ◽  
Powder Mixtures ◽  
Thermodynamics And Kinetics ◽  
Transmission Electron ◽  
Kinetics Of

The microstructural evolution, thermodynamics and kinetics of Mo-21%Tm2O3 (mass fraction, %) powder mixtures during ball milling were investigated using X-ray diffraction and transmission electron microscopy. Ball milling induced Tm2O3 to be decomposed and then dissolved into Mo crystal. The supersaturated nanocrystalline solid solution of Mo (Tm, O) was obtained after 96 h of ball milling. The elements of Mo, Tm and O were distributed uniformly in the ball-milled particles. Based on the semi-experimental theory of Miedema, a thermodynamic model was developed to calculate the driving force of phase evolution. There was no chemical driving force to form a crystal solid solution of Tm atoms in Mo crystal or an amorphous phase because the Gibbs free energy for both processes was higher than zero. For Mo-21%Tm2O3, it was mechanical work, not negative heat of mixing, that provided the driving force to form supersaturated nanocrystalline Mo (Tm, O) solid solution.

scholarly journals Microstructural Evolution, Thermodynamics, and Kinetics of Mo-Tm2O3 Powder Mixtures during Ball Milling

Materials ◽  
2016 ◽  
Vol 9 (10) ◽  
pp. 834 ◽  
Author(s):  
Yong Luo ◽  
Guang Ran ◽  
Nanjun Chen ◽  
Qiang Shen ◽  
Yaoli Zhang
Keyword(s):  
Ball Milling ◽  
Microstructural Evolution ◽  
Powder Mixtures ◽  
Thermodynamics And Kinetics ◽  
Kinetics Of

scholarly journals Facile Preparation of Granular Copper Films as Cathode for Enhanced Electrochemical Degradation of Methyl Orange

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2697
Author(s):  
Jiajie Xing ◽  
Min Song ◽  
Mengyao Yang ◽  
Xu Tan ◽  
Fenglin Li ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Room Temperature ◽  
Ph Value ◽  
Copper Films ◽  
Electrochemical Degradation ◽  
Degradation Reaction ◽  
Facile Preparation ◽  
Neutral Conditions ◽  
Kinetics Of ◽  
Degradation Of Methyl Orange

In this paper, granular copper films (GCFs) were prepared through electrodeposition in CuSO4 solution containing triethanolamine, and the films were used as electro-Fenton-like cathodes for degradation of methyl orange (MO). The effects of triethanolamine concentration, pH value, current intensity and temperature on the morphology of the films, as well as the MO decolorization ratio (DR), were investigated in detail. Results show that when the concentration of triethanolamine is 0.2 wt%, the prepared GCF exhibits the best performance. Under room temperature and neutral conditions, no external O2 or catalyst, MO is completely decolorized after 240 min. Compared with the commonly used carbon cathode, the GCF cathode can increase the MO decolorization rate by approximately 70.9%. The kinetics of the electrochemical degradation reaction is also discussed.

Irradiation behavior of pyrolytic silicon carbide

1983 ◽  
Vol 41 ◽  
pp. 72-73
Author(s):  
R. J. Lauf
Keyword(s):  
Silicon Carbide ◽  
Fission Products ◽  
Thermodynamics And Kinetics ◽  
Neutron Fluences ◽  
Fuel Particles ◽  
Sic Coatings ◽  
Irradiation Behavior ◽  
Kinetics Of ◽  
Htgr Fuel

Fuel particles for the High-Temperature Gas-Cooled Reactor (HTGR) contain a layer of pyrolytic silicon carbide to act as a miniature pressure vessel and primary fission product barrier. Optimization of the SiC with respect to fuel performance involves four areas of study: (a) characterization of as-deposited SiC coatings; (b) thermodynamics and kinetics of chemical reactions between SiC and fission products; (c) irradiation behavior of SiC in the absence of fission products; and (d) combined effects of irradiation and fission products. This paper reports the behavior of SiC deposited on inert microspheres and irradiated to fast neutron fluences typical of HTGR fuel at end-of-life.

Investigation of irradiation-induced nucleation processes in silicon and germanium

1995 ◽  
Vol 53 ◽  
pp. 224-225
Author(s):  
Harry A. Atwater ◽  
C.M. Yang ◽  
K.V. Shcheglov
Keyword(s):  
Room Temperature ◽  
Crystal Size ◽  
Initial Distribution ◽  
Engineering Control ◽  
Size Evolution ◽  
Silicon And Germanium ◽  
Ge Quantum Dot ◽  
And Control ◽  
Germanium Quantum Dots ◽  
Kinetics Of

Studies of the initial stages of nucleation of silicon and germanium have yielded insights that point the way to achievement of engineering control over crystal size evolution at the nanometer scale. In addition to their importance in understanding fundamental issues in nucleation, these studies are relevant to efforts to (i) control the size distributions of silicon and germanium “quantum dots𠇍, which will in turn enable control of the optical properties of these materials, (ii) and control the kinetics of crystallization of amorphous silicon and germanium films on amorphous insulating substrates so as to, e.g., produce crystalline grains of essentially arbitrary size.Ge quantum dot nanocrystals with average sizes between 2 nm and 9 nm were formed by room temperature ion implantation into SiO2, followed by precipitation during thermal anneals at temperatures between 30°C and 1200°C[1]. Surprisingly, it was found that Ge nanocrystal nucleation occurs at room temperature as shown in Fig. 1, and that subsequent microstructural evolution occurred via coarsening of the initial distribution.

Comparative Labelling and Biokinetic Studies of 99mTc-EDTA(Sn) and 99mTc-DTPA(Sn)

1977 ◽  
Vol 16 (01) ◽  
pp. 30-35 ◽  
Author(s):  
N. Agha ◽  
R. B. R. Persson
Keyword(s):  
Complex Formation ◽  
Significant Influence ◽  
Room Temperature ◽  
Ph Value ◽  
Maximum Activity ◽  
Reduction Step ◽  
Labelling Yield ◽  
Different Temperatures ◽  
Kinetics Of

SummaryGelchromatography column scanning has been used to study the fractions of 99mTc-pertechnetate, 99mTcchelate and reduced hydrolyzed 99mTc in preparations of 99mTc-EDTA(Sn) and 99mTc-DTPA(Sn). The labelling yield of 99mTc-EDTA(Sn) chelate was as high as 90—95% when 100 μmol EDTA · H4 and 0.5 (Amol SnCl2 was incubated with 10 ml 99mTceluate for 30—60 min at room temperature. The study of the influence of the pH-value on the fraction of 99mTc-EDTA shows that pH 2.8—2.9 gave the best labelling yield. In a comparative study of the labelling kinetics of 99mTc-EDTA(Sn) and 99mTc- DTPA(Sn) at different temperatures (7, 22 and 37°C), no significant influence on the reduction step was found. The rate constant for complex formation, however, increased more rapidly with increased temperature for 99mTc-DTPA(Sn). At room temperature only a few minutes was required to achieve a high labelling yield with 99mTc-DTPA(Sn) whereas about 60 min was required for 99mTc-EDTA(Sn). Comparative biokinetic studies in rabbits showed that the maximum activity in kidneys is achieved after 12 min with 99mTc-EDTA(Sn) but already after 6 min with 99mTc-DTPA(Sn). The long-term disappearance of 99mTc-DTPA(Sn) from the kidneys is about five times faster than that for 99mTc-EDTA(Sn).

Thermodynamics and kinetics of hydriding of the Zr(Ni0.75V0.25)2 laves phase

2004 ◽  
Vol 29 (2) ◽  
pp. 1-9
Author(s):  
Mustapha Boulghallat ◽  
Ahmed Jouaiti ◽  
Norbert Gérard
Keyword(s):  
Laves Phase ◽  
Thermodynamics And Kinetics ◽  
Kinetics Of

Kinetics of the Thermal Disappearance of Radicals Formed During the Radiolysis of Aspartic Acid

2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihai Contineanu ◽  
iulia Contineanu ◽  
Ana Neacsu ◽  
Stefan Perisanu
Keyword(s):  
Thermal Resistance ◽  
Aspartic Acid ◽  
Room Temperature ◽  
Esr Spectra ◽  
Complex Mechanism ◽  
Radical Species ◽  
Mechanisms Of Formation ◽  
Kinetics Of

The radiolysis of the isomers L-, D- and DL- of the aspartic acid, in solid polycrystalline state, was investigated at room temperature. The analysis of their ESR spectra indicated the formation of at least two radicalic entities. The radical, identified as R3, resulting from the deamination of the acid, exhibits the highest concentration and thermal resistance. Possible mechanisms of formation of three radical species are suggested, based also on literature data. The kinetics of the disappearance of radical R3 indicated a complex mechanism. Three possible variants were suggested for this mechanism.

Sign in / Sign up

Export Citation Format

Share Document