scholarly journals Транспортные процессы с участием атомов углерода между поверхностью и объемом родия при образовании и разрушении графена

2020 ◽  
Vol 54 (6) ◽  
pp. 552
Author(s):  
Е.В. Рутьков ◽  
Е.Ю. Афанасьева ◽  
Н.Р. Галль
Keyword(s):  
Phase Transition ◽  
Activation Energy ◽  
Temperature Dependence ◽  
Atomic Carbon ◽  
Graphene Growth ◽  
Carbon Dissolution ◽  
The Difference ◽  
Kinetics Of

Equilibrium transport of atomic carbon between Rh surface and bulk has been studied. This transport controls the kinetics of the phase transition resulting in graphene growth or destruction. The difference ΔE=0.7 eV has been measured between the activation energy of atomic carbon dissolution E1s and that of its segregation from the bulk to the surface E1s. The temperature dependence of chemisorbed carbon critical cover Neq = Neq(T) has been measured, that is the cover when 2D phase transition takes place and graphene islands start to grow. E.g., Neq = 7.7•1014 cm-2 at T = 1800 K, and Neq = 3.1•1014 cm-2 at T = 1000 K.

Study on the Melting Mechanism of Maleic Anhydride

2020 ◽  
Vol 10 (1) ◽  
pp. 65-78
Author(s):  
Bratati Das ◽  
Ashis Bhattacharjee
Keyword(s):  
Phase Transition ◽  
Activation Energy ◽  
Maleic Anhydride ◽  
Temperature Dependence ◽  
Growth Models ◽  
Melting Process ◽  
Nucleation And Growth ◽  
Crystalline Solid ◽  
Scanning Calorimetry ◽  
Melting Mechanism

Background: Melting of a pure crystalline material is generally treated thermodynamically which disregards the dynamic aspects of the melting process. According to the kinetic phenomenon, any process should be characterized by activation energy and preexponential factor where these kinetic parameters are derivable from the temperature dependence of the process rate. Study on such dependence in case of melting of a pure crystalline solid gives rise to a challenge as such melting occurs at a particular temperature only. The temperature region of melting of pure crystalline solid cannot be extended beyond this temperature making it difficult to explore the temperature dependence of the melting rate and consequently the derivation of the related kinetic parameters. Objective: The present study aims to explore the mechanism of the melting process of maleic anhydride in the framework of phase transition models. Taking this process as just another first-order phase transition, occurring through the formation of nuclei of new phase and their growth, particular focus is on the nucleation and growth models. Methods: Non-isothermal thermogravimetry, as well as differential scanning calorimetry studies, has been performed. Using isoconversional kinetic analysis, temperature dependence of the activation energy of melting has been obtained. Nucleation and growth models have been utilized to obtain the theoretical temperature dependencies for the activation energy of melting and these dependencies are then compared with the experimentally estimated ones. Conclusion: The thermogravimetry study indicates that melting is followed by concomitant evaporation, whereas the differential scanning calorimetry study shows that the two processes appear in two different temperature regions, and these differences observed may be due to the applied experimental conditions. From the statistical analysis, the growth model seems more suitable than the nucleation model for the interpretation of the melting mechanism of the maleic anhydride crystals.

scholarly journals Phase Transformation Kinetics of a FCC Al0.25CoCrFeNi High-Entropy Alloy during Isochronal Heating

Metals ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 1015
Author(s):  
Jun Wang ◽  
Chen Wei ◽  
Haoxue Yang ◽  
Tong Guo ◽  
Tingting Xu ◽  
...  
Keyword(s):  
Phase Transition ◽  
Activation Energy ◽  
Phase Transformation ◽  
High Entropy Alloy ◽  
Transformation Kinetics ◽  
High Entropy ◽  
Phase Transformation Kinetics ◽  
Diffusion Controlled ◽  
Thermal Dilation ◽  
Kinetics Of

The phase transformation kinetics of a face-centered-cubic (FCC) Al0.25CoCrFeNi high-entropy alloy during isochronal heating is investigated by thermal dilation experiment. The phase transformed volume fraction is determined from the thermal expansion curve, and results show that the phase transition is controlled by diffusion controlled nucleation-growth mechanism. The kinetic parameters, activation energy and kinetic exponent are determined based on Kissinger–Akahira–Sunose (KAS) and Johnson–Mehl–Avrami (JMA) method, respectively. The activation energy and kinetic exponent determined are almost constant, indicating a stable and slow speed of phase transition in the FCC Al0.25CoCrFeNi high-entropy alloy. During the main transformation process, the kinetic exponent shows that the phase transition is diffusion controlled process without nucleation during the transformation.

scholarly journals Activation Energies and Temperature Dependencies of the Rates of Crystallization and Melting of Polymers

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1070 ◽  
Author(s):  
Sergey Vyazovkin
Keyword(s):  
Experimental Data ◽  
Phase Transition ◽  
Activation Energy ◽  
Temperature Dependence ◽  
Kinetic Analysis ◽  
Review Paper ◽  
Isoconversional Methods ◽  
Activation Energies ◽  
Phase Transition Kinetics ◽  
Kinetic Treatment

The objective of this review paper is to survey the phase transition kinetics with a focus on the temperature dependence of the rates of crystallization and melting, as well as on the activation energies of these processes obtained via the Arrhenius kinetic treatment, including the treatment by isoconversional methods. The literature is analyzed to track the development of the basic models and their underlying concepts. The review presents both theoretical and practical considerations regarding the kinetic analysis of crystallization and melting. Both processes are demonstrated to be kinetically complex, and this is revealed in the form of nonlinear Arrhenius plots and/or the variation of the activation energy with temperature. Principles which aid one to understand and interpret such results are discussed. An emphasis is also put on identifying proper computational methods and experimental data that can lead to meaningful kinetic interpretation.

Temperature dependence of photocatalytic CO2reduction by trans(Cl)–Ru(bpy)(CO)2Cl2: activation energy difference between CO and formate production

2017 ◽  
Vol 198 ◽  
pp. 263-277 ◽  
Author(s):  
Hitoshi Ishida ◽  
Akihiko Sakaba
Keyword(s):  
Activation Energy ◽  
Carbon Monoxide ◽  
Temperature Dependence ◽  
Catalytic System ◽  
Energy Difference ◽  
Catalytic Cycle ◽  
The Difference ◽  
A Minor ◽  
Increasing Temperature ◽  
Formate Production

The temperature dependence of photocatalytic CO2reduction bytrans(Cl)–Ru(bpy)(CO)2Cl2(bpy: 2,2′-bipyridine) has been researched in ethanol (EtOH)/N,N-dimethylacetamide (DMA) solutions containing [Ru(bpy)3]2+(a photosensitizer) and 1-benzyl-1,4-dihydronicotinamide (BNAH, an electron donor). The catalytic system efficiently reduces CO2to carbon monoxide (CO) with formate (HCOO−) as a minor product. The mechanism of the catalysis consists of the electron-relay cycle and the catalytic cycle: in the former cycle the photochemically generated reduced species of the photosensitizer injects an electron to the catalyst, and in the latter the catalyst reduces CO2. At a low concentration of the catalyst (5.0 μM), where the catalytic cycle is rate-determining, the temperature dependence of CO/HCOO−is also dependent on the EtOH contents: the selectivity of CO/HCOO−decreases in 20% and 40%-EtOH/DMA with increasing temperature, while it increases in 60%-EtOH/DMA. The temperature dependence of the CO/HCOO−selectivity indicates that the difference in activation energy (ΔΔG‡) between CO and HCOO−production is estimated asca.3.06 kJ mol−1in 40%-EtOH/DMA at 298 K.

Effect of Molecular Weight, Shape of the Molecule, and Presence of Polar Groups on the Autohesion of High Polymers. III

1957 ◽  
Vol 30 (2) ◽  
pp. 548-554 ◽  
Author(s):  
S. S. Voyutskiĭ ◽  
B. V. Shtarkh
Keyword(s):  
Activation Energy ◽  
Molecular Weight ◽  
Temperature Dependence ◽  
Structural Changes ◽  
Chain Molecule ◽  
Complete Disappearance ◽  
Short Side ◽  
Polar Groups ◽  
Kinetics Of ◽  
High Polymers

Abstract 1. It is shown for polyisobutylenes of different molecular weight that increase in the size of the chain molecule retards autohesion, but increases the limiting value to which the work of autohesion tends with increasing contact time. 2. Investigation of the temperature dependence of autohesion of polyisobutylenes showed that the activation energy does not depend on the molecular weight of the polyisobutylene. 3. It is shown for polybutadienes with varying contents of 1,4- and 1,2-structures that autohesion decreases with increase in the number of short side groups in the molecule, which apparently hinder diffusion by purely steric causes. 4. Investigation of the temperature dependence of autohesion of butadienenitrile copolymers with different contents of acrylonitrile in the molecule showed that the activation energy of autohesion increases with increase of polar nitrile groups in the polymer. 5. It is shown for the vulcanization of natural rubber that the formation of a spatial structure results in complete disappearance of autohesion in high polymers. It is shown that the kinetics of changes of autohesion during vulcanization can effectively characterize the structural changes which take place in the polymer during the process.

scholarly journals Co-combustion interactions between teak sawdust and sewage sludge with additives

BioResources ◽  
2019 ◽  
Vol 14 (1) ◽  
pp. 1466-1481
Author(s):  
Haobin Peng ◽  
Yuesheng Li ◽  
Guohua Chen ◽  
Yunquan Li
Keyword(s):  
Activation Energy ◽  
Sewage Sludge ◽  
Loss Rate ◽  
Thermal Characteristics ◽  
Ignition Point ◽  
Exponential Factor ◽  
Characteristic Values ◽  
The Difference ◽  
Combustion Behaviors ◽  
Kinetics Of

The thermal characteristics and kinetics of teak sawdust (TS), sewage sludge (SS), and their blends were evaluated during combustion by thermogravimetric analysis (TGA). The samples were prepared as pure fuel, TS and SS; blends, where TS was mixed with SS at the ratios of 75:25, 50:50, and 25:75; and as fuels with additives, where the fuels above were mixed with activated carbon (AC), CaO, MgO, and ZnO individually at a proportion of 5 wt%. Some characteristic values of combustion were evaluated, such as Ti, Tb, and Mf, and the combustion behaviors of the fuels were compared. The difference between measurement and weighted calculation of the weight left proportion (∆M), weight loss rate (∆DTG), and activation energy (∆E) were introduced for analysis. Blending with teak sawdust improved the combustion performance of sewage sludge. As the content of the sewage sludge increased, the pre-exponential factor varied from 1.76 x 105 s-1(100T) to 1.01 x 101 s-1(100S), while the global activation energy decreased from 74 kJ/mol (100T) to 38 kJ/mol (100S). Sewage sludge burned more completely when blended with teak sawdust at ratios of greater than 50 wt%. All four additives inhibited the oxidation of the blends around the ignition point.

The Temperature Dependence of the Atoms Co Diffusion Coefficient in Pt80Co20(111) Alloy

2007 ◽  
Vol 265 ◽  
pp. 19-23
Author(s):  
M. Vasylyev ◽  
Vitaliy A. Tinkov ◽  
Sergey I. Sidorenko ◽  
S.M. Voloshko
Keyword(s):  
Activation Energy ◽  
Diffusion Coefficient ◽  
Temperature Dependence ◽  
Surface Segregation ◽  
Surface Region ◽  
Near Surface ◽  
Kinetics Of

The method of Ionization Spectroscopy is used to study the thermo-induced kinetics of surface segregation of the Pt80Co20(111) alloy components. The temperature dependence of the Co diffusion coefficient in this alloy is determined. It is found that the value of the activation energy for the segregation of Co atoms in the near-surface region is close to the heat of sublimation of pure Co.

Generalised kinetics of overall phase transition useful for glass crystallisation when assuming non-isothermal conditions

2020 ◽  
Vol 61 (6) ◽  
pp. 209-212 ◽  
Author(s):  
Isak Avramov ◽  
◽  
Jaroslav Šesták ◽  
Keyword(s):  
Experimental Data ◽  
Phase Transition ◽  
Activation Energy ◽  
Heating Rate ◽  
Characteristic Temperature ◽  
Isothermal Conditions ◽  
Constant Rate ◽  
Avrami Parameter ◽  
Kinetics Of ◽  
Glass Crystallisation

The modelling of reaction kinetics is a fashionable subject of publications. We developed an analogue of the KJMA equation under non-isothermal conditions α(T)=1−exp(−(T/θ)N) that describes the dependence of degree of transformation α(T) at a constant rate, q, of heating with characteristic temperature θ(q) and power N, proportional to the Avrami parameter, n. This equation is valid even when the activation energy of the process is not constant. We demonstrate that reliable information about the activation energy is obtained when the experimental data are plotted in coordinates: logq (heating rate) against logTp (peak temperature).

Temperature Dependence of the Photoinduced Degradation and Annealing in a-Si:H

2000 ◽  
Vol 609 ◽  
Author(s):  
Niko Schultz ◽  
P. Craig Taylor
Keyword(s):  
Temperature Dependence ◽  
Room Temperature ◽  
Dangling Bond ◽  
Defect States ◽  
Slow Increase ◽  
Spin Resonance ◽  
The Difference ◽  
Kinetics Of ◽  
Defect Densities ◽  
Spin Densities

ABSTRACTWe investigated the temperature dependence of the production and annealing kinetics of the light induced defect states in a:Si:H by electron spin resonance (ESR). At low temperatures (T ∼ 25 K) the silicon dangling bond production is about half as efficient as it is at 300 K. Defects, which are created below about 100 K, almost entirely anneal at room temperature. A sample of a-Si:H, which is subjected to several photo-excitation and annealing cycles, shows a very slow increase of both the degraded and annealed defect densities. The difference in the spin densities between the annealed and degraded states decreases with an increasing number of degradation/annealing cycles.

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