Dependence of activation energy and pre-exponential factor on electric field in bulk Se90Sb10−xAgx glassy alloys

2014 ◽  
Vol 386 ◽  
pp. 51-55 ◽  
Author(s):  
Anjani Kumar ◽  
A. Kumar
1978 ◽  
Vol 21 (85) ◽  
pp. 259-276 ◽  
Author(s):  
G. P. Johari ◽  
S. J. Jones

AbstractThe relative permittivity and loss of zone-refined single crystals of hexagonal ice have been measured in the temperature range 200–271 K and frequency range 0.5 HZ–0.2 MHz, using brass, stainless steel, and gold-foil electrodes. The c-axis of the crystal was oriented parallel to the electric field in 14 samples and perpendicular to the field in 8 samples. The equilibrium relative permittivity of orientation polarization ϵ0, parallel and perpendicular to the c-axis, is 96.5±1 and the average relaxation time τay is 36 μs at 265±0.5K; ϵ0 = 124±1.5 and τav = 30 ms, at 210 K. The magnitude of the orientation polarization obeys the Curie-Weiss equation with T0= 15±2 K for both the orientations. These values are in contrast with the c. 17% difference in ϵo for the two orientations reported in the literature. The extrapolated limiting high-frequency relative permittivity ϵ∞, measured for both the orientations, is indistinguishable within 0.5%.The logarithmic plot of the product of τav and temperature against the reciprocal temperature is linear in the range 210–271 K and gives an activation energy and a pre-exponential factor of 51±2 kJ mol–1 and 0.93±0.22 ps K respectively, for both the orientations of the c-axis with respect to the electric field. The decrease in activation energy which has been reported to occur in polycrystalline ice and in single crystal ice near 230 K is not found until a temperature of 210 K. Single crystals of ice stored in the dielectric cell, after the completion of measurements, for periods ranging from 1–11 weeks at 253±2 K showed no change in their ϵ0, τav, ϵ∞ that could be attributed to the effect of ageing on the orientation polarization.


1978 ◽  
Vol 21 (85) ◽  
pp. 259-276 ◽  
Author(s):  
G. P. Johari ◽  
S. J. Jones

Abstract The relative permittivity and loss of zone-refined single crystals of hexagonal ice have been measured in the temperature range 200–271 K and frequency range 0.5 HZ–0.2 MHz, using brass, stainless steel, and gold-foil electrodes. The c-axis of the crystal was oriented parallel to the electric field in 14 samples and perpendicular to the field in 8 samples. The equilibrium relative permittivity of orientation polarization ϵ0, parallel and perpendicular to the c-axis, is 96.5±1 and the average relaxation time τay is 36 μs at 265±0.5K; ϵ0 = 124±1.5 and τav = 30 ms, at 210 K. The magnitude of the orientation polarization obeys the Curie-Weiss equation with T 0 = 15±2 K for both the orientations. These values are in contrast with the c. 17% difference in ϵo for the two orientations reported in the literature. The extrapolated limiting high-frequency relative permittivity ϵ∞, measured for both the orientations, is indistinguishable within 0.5%. The logarithmic plot of the product of τav and temperature against the reciprocal temperature is linear in the range 210–271 K and gives an activation energy and a pre-exponential factor of 51±2 kJ mol–1 and 0.93±0.22 ps K respectively, for both the orientations of the c-axis with respect to the electric field. The decrease in activation energy which has been reported to occur in polycrystalline ice and in single crystal ice near 230 K is not found until a temperature of 210 K. Single crystals of ice stored in the dielectric cell, after the completion of measurements, for periods ranging from 1–11 weeks at 253±2 K showed no change in their ϵ0, τav, ϵ∞ that could be attributed to the effect of ageing on the orientation polarization.


2006 ◽  
Vol 319 ◽  
pp. 139-144 ◽  
Author(s):  
Masuyuki Hasegawa ◽  
M. Takeuchi ◽  
D. Nagata ◽  
T. Wada ◽  
Hidemi Kato ◽  
...  

The hydrogen-induced internal friction and mechanical strength of the Ti-rich Ti34Zr11Cu47Ni8 and (Ti34Zr11Cu47Ni8)98Si2 hydrogenated glassy alloys have been investigated. It is found that the tensile strength is more than 0.8 GPa at room temperature when the hydrogen content is below about 20 at% for both alloys. The frequency dependence of peak temperature of the hydrogen-induced internal friction of (Ti34Zr11Cu47Ni8)98Si2-17.3 at%H hydrogenated glassy alloys has been clarified. Activation energy and pre-exponential factor are estimated to be 0.35 eV and 1.3x10-12, respectively. Compared with these values with those of Zr40Cu49Al10Si1 hydrogenated glassy alloys which show an internal friction peak around 300 K at about 300 Hz, it is found that the activation energy is much smaller than that of the latter although the pre-exponential factor is almost the same. Considering their similar composition and different component (Al), it is suggested that the component Al of the latter glassy alloys is effective for the higher activation energy which results in the increase of the peak temperature.


2016 ◽  
Vol 10 (3) ◽  
pp. 137-142
Author(s):  
Karishma Singh ◽  
Neeraj Mehta ◽  
Sudhir Sharma ◽  
Ashok Kumar

Glassy alloys of Se90In10-xAgx were prepared using melt quenching technique. Non-isothermal differential scanning calorimetric (DSC) studies were done on Se90In10-xAgx (x = 0, 2, 4, 6, 8 at.%) glassy alloys at four different heating rates (? = 5, 10, 15, 20?C/min). Well defined endothermic and exothermic peaks were obtained at glass transition (Tg) and crystallization temperature (Tc), respectively. Augis and Bennett?s method was used to obtain the composition dependent crystallization activation energy (Ec) and the pre-exponential factor (?0) of the Arrhenius expression. A linear dependence between ln ?0 and Ec was observed showing the existence of compensation effects of the Meyer-Neldel type. These compensation effects confirm the applicability of Meyer-Neldel (MN) rule for the non-isothermal crystallization in the present case.


Author(s):  
Niels Engholm Henriksen ◽  
Flemming Yssing Hansen

This chapter reviews the microscopic interpretation of the pre-exponential factor and the activation energy in rate constant expressions of the Arrhenius form. The pre-exponential factor of apparent unimolecular reactions is, roughly, expected to be of the order of a vibrational frequency, whereas the pre-exponential factor of bimolecular reactions, roughly, is related to the number of collisions per unit time and per unit volume. The activation energy of an elementary reaction can be interpreted as the average energy of the molecules that react minus the average energy of the reactants. Specializing to conventional transition-state theory, the activation energy is related to the classical barrier height of the potential energy surface plus the difference in zero-point energies and average internal energies between the activated complex and the reactants. When quantum tunnelling is included in transition-state theory, the activation energy is reduced, compared to the interpretation given in conventional transition-state theory.


2016 ◽  
Vol 138 (5) ◽  
Author(s):  
Anil Kumar Varma ◽  
Prasenjit Mondal

The present study was conducted to investigate the physicochemical properties and pyrolysis kinetics of sugarcane bagasse (SB). The physiochemical properties of SB were determined to examine its potential for pyrolysis. The physiochemical properties such as proximate analysis, ultimate analysis, heating values, lignocellulosic composition, X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) of SB were investigated. The pyrolysis experiments were conducted in a nonisothermal thermogravimetric analyzer (TGA) to understand the thermal degradation behavior of SB. The activation energy (Ea) of SB pyrolysis was calculated by model-free Kissinger–Akahira–Sunose (KAS) and Ozawa–Flynn–Wall (OFW) methods. Average values of activation energy determined through KAS and OFW methods are found as 91.64 kJ/mol and 104.43 kJ/mol, respectively. Variation in the activation energy with degree of conversion was observed, which shows that pyrolysis is a complex process composed of several reactions. Coats–Redfern method was used to calculate the pre-exponential factor and reaction order. Conversion of SB due to heat treatment computed by using the kinetic parameters is found to be in good agreement with the experimental conversion data, and the maximum error limit between the experimental and predicted conversions is 8.5% for 5 °C/min, 6.0% for 10 °C/min, and 11.6% for 20 °C/min. The current investigation proves the suitability of SB as a potential feedstock for pyrolysis.


2010 ◽  
Vol 297-301 ◽  
pp. 1301-1305
Author(s):  
Anatoly Yakovlevich Fishman ◽  
Tatiana Eugenievna Kurennykh ◽  
Vladimir Borisovich Vykhodets ◽  
V.B. Vykhodets

Isotope exchange of oxygen 18О2 with the boundary of nanograins of oxide LaMnO3+ obtained by the method of shock-wave loading was investigated in the temperature range of 400 – 500 °C. It was established that the temperature dependence of the isotope exchange rate is described by the Arrhenius expression, the activation energy and the pre-exponential factor being 1.67 eV and 1.8∙102 cm/s, respectively. Comparison with literature data has shown that for oxide LaMnO3+, a significant difference in activation energies and pre-exponential factors is observed for the isotope exchange rate with a ‘defect-free’ surface and the nanograin boundary. In case of the boundary, these parameters were higher: the activation energy about two times, and the pre-exponential factor, by almost 7 orders of magnitude.


2019 ◽  
Vol 97 (11) ◽  
pp. 795-804 ◽  
Author(s):  
Dong Xiang ◽  
Weihua Zhu

The density functional tight-binding molecular dynamics approach was used to study the mechanisms and kinetics of initial pyrolysis and combustion reactions of isolated and multi-molecular FOX-7. Based on the thermal cleavage of bridge bonds, the pyrolysis process of FOX-7 can be divided into three stages. However, the combustion process can be divided into five decomposition stages, which is much more complex than the pyrolysis reactions. The vibrations in the mean temperature contain nodes signifying the formation of new products and thereby the transitions between the various stages in the pyrolysis and combustion processes. Activation energy and pre-exponential factor for the pyrolysis and combustion reactions of FOX-7 were obtained from the kinetic analysis. It is found that the activation energy of its pyrolysis and combustion reactions are very low, making both take place fast. Our simulations provide the first atomic-level look at the full dynamics of the complicated pyrolysis and combustion process of FOX-7.


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