Calorimetric Studies of Dissolution Kinetics of Ni2(Cr,Mo) Phase in Ni-Cr-Mo Alloys Using Non-Isothermal Approach

2008 ◽  
Vol 279 ◽  
pp. 111-116 ◽  
Author(s):  
H.C. Pai ◽  
Bikas C. Maji ◽  
A. Biswas ◽  
Madangopal Krishnan ◽  
M. Sundararaman
Keyword(s):  
Activation Energy ◽  
Dissolution Kinetics ◽  
Scanning Calorimetry ◽  
Alloy Matrix ◽  
Nickel Chromium ◽  
Chromium Alloys ◽  
Kinetics Of Dissolution ◽  
Calorimetric Studies ◽  
Kinetics Of ◽  
Complex Nickel

The kinetics of dissolution of ordered phase with Pt2Mo structure has been studied in two nickel chromium alloys – one without molybdenum and another with molybdenum - using differential scanning calorimetry. The activation energy for dissolution, determined using three nonisothermal approaches was found to be ~ 418 kJ /mole for both the alloys. This value agreed very well with the activation energy for coarsening of g″ precipitates in Ni-Cr-Mo matrix and is close to activation energy for mobility of chromium and molybdenum in complex nickel alloy matrix.

scholarly journals Non-Isothermal Sublimation Kinetics of 2,4,6-Trinitrotoluene (TNT) Nanofilms

Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1163 ◽  
Author(s):  
Walid Hikal ◽  
Brandon Weeks
Keyword(s):  
Activation Energy ◽  
Analytical Techniques ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Absorbance Spectroscopy ◽  
Calculated Activation Energy ◽  
Sublimation Kinetics ◽  
Sublimation Rates ◽  
First Time ◽  
Kinetics Of

Non-isothermal sublimation kinetics of low-volatile materials is more favorable over isothermal data when time is a crucial factor to be considered, especially in the subject of detecting explosives. In this article, we report on the in-situ measurements of the sublimation activation energy for 2,4,6-trinitrotoluene (TNT) continuous nanofilms in air using rising-temperature UV-Vis absorbance spectroscopy at different heating rates. The TNT films were prepared by the spin coating deposition technique. For the first time, the most widely used procedure to determine sublimation rates using thermogravimetry analysis (TGA) and differential scanning calorimetry (DSC) was followed in this work using UV-Vis absorbance spectroscopy. The sublimation kinetics were analyzed using three well-established calculating techniques. The non-isothermal based activation energy values using the Ozawa, Flynn–Wall, and Kissinger models were 105.9 ± 1.4 kJ mol−1, 102.1 ± 2.7 kJ mol−1, and 105.8 ± 1.6 kJ mol−1, respectively. The calculated activation energy agreed well with our previously reported isothermally-measured value for TNT nanofilms using UV-Vis absorbance spectroscopy. The results show that the well-established non-isothermal analytical techniques can be successfully applied at a nanoscale to determine sublimation kinetics using absorbance spectroscopy.

Thermodynamics kinetics of boron carbide under gamma irradiation dose

2019 ◽  
Vol 33 (09) ◽  
pp. 1950073 ◽  
Author(s):  
Matlab Mirzayev ◽  
Ertugrul Demir ◽  
Khagani Mammadov ◽  
Ravan Mehdiyeva ◽  
Sakin Jabarov ◽  
...  
Keyword(s):  
Activation Energy ◽  
Boron Carbide ◽  
Gamma Irradiation ◽  
Irradiation Time ◽  
Energy Levels ◽  
Initial State ◽  
Scanning Calorimetry ◽  
Gas Atmosphere ◽  
Quantitative Changes ◽  
Kinetics Of

In this paper, high purity boron carbide samples were irradiated by [Formula: see text]Co gamma radioisotope source (0.27 Gy/s dose rate) with 50, 100, 150 and 200 irradiation hours at room-temperature. The unirradiated and irradiated boron carbide samples were heated from 30[Formula: see text]C to 1000[Formula: see text]C at a heating rate of 5[Formula: see text]C/min under the argon gas atmosphere of flow rate 20 ml/min. Thermogravimetric (TG) and Differential Scanning Calorimetry (DSC) were carried out in order to understand the thermodynamic kinetics of boron carbide samples. The weight kinetics, activation energy and specific heat capacity of the unirradiated and irradiated boron carbide samples were examined in two parts, T [Formula: see text] 650[Formula: see text]C and T [Formula: see text] 650[Formula: see text]C, according to the temperature. The dynamic of quantitative changes in both ranges is different depending on the irradiation time. While the phase transition of unirradiated boron carbide samples occurs at 902[Formula: see text]C, this value shifts upto 940[Formula: see text]C in irradiated samples depending on the irradiation time. The activation energy of the unirradiated boron carbide samples decreased from 214 to 46 J/mol in the result of 200[Formula: see text]h gamma irradiation. The reduction of the activation energy after the irradiation compared to the initial state shows that the dielectric properties of the irradiated boron carbide samples have been improved. After the gamma irradiation, two energy barrier states depending on the absorption dose of samples were formed in the irradiated samples. The first and second energy barriers occurred in 0.56–0.80 and 0.23–0.36 eV energy intervals, respectively. The existence of two energy levels in the irradiated boron carbide indicates that the point defects are at deep levels, close to the valence band.

Study on Curing Kinetics of MEP-15/593/660 System

2014 ◽  
Vol 988 ◽  
pp. 31-35
Author(s):  
Jia Le Song ◽  
Chan Chan Li ◽  
Zhi Mi Zhou ◽  
Chao Qiang Ye ◽  
Wei Guang Li
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Kinetic Parameters ◽  
Curing Kinetics ◽  
Conversion Ratio ◽  
Scanning Calorimetry ◽  
Degree Of Cure ◽  
Curing Kinetic ◽  
The Relationship ◽  
Kinetics Of

Curing kinetics of MEP-15/593 system and MEP-15/593/660 system is studied by means of differential scanning calorimetry (DSC). Curing kinetic parameters are evaluated and the relationship between diluent 660 and the curing properties is investigated. The results show that the diluent 660 can not only reduce viscosity and activation energy, but also improve the degree of cure and conversion ratio.

scholarly journals Thermal Analysis On The Kinetics Of Magnesium-Aluminum Layered Double Hydroxides In Different Heating Rates

2015 ◽  
Vol 60 (2) ◽  
pp. 1357-1359 ◽  
Author(s):  
Y. Hongbo ◽  
C. Meiling ◽  
W. Xu ◽  
G. Hong
Keyword(s):  
Activation Energy ◽  
Thermal Analysis ◽  
Layered Double Hydroxides ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Exponential Factor ◽  
Thermal Kinetic Parameters ◽  
Double Hydroxides ◽  
Kinetics Of ◽  
Dsc Curves

Abstract The thermal decomposition of magnesium-aluminum layered double hydroxides (LDHs) was investigated by thermogravimetry analysis and differential scanning calorimetry (DSC) methods in argon environment. The influence of heating rates (including 2.5, 5, 10, 15 and 20K/min) on the thermal behavior of LDHs was revealed. By the methods of Kissinger and Flynn-Wall-Ozawa, the thermal kinetic parameters of activation energy and pre-exponential factor for the exothermic processes under non-isothermal conditions were calculated using the analysis of corresponding DSC curves.

Study on the β1→α+β2 Transformation Kinetics of Ti-6Al-4V Alloy by DSC

2014 ◽  
Vol 508 ◽  
pp. 110-113
Author(s):  
Rong Hua Zhang ◽  
Biao Wu ◽  
Xiao Ping Zheng
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Phase Transformation ◽  
Cooling Rate ◽  
Volume Fraction ◽  
Avrami Exponent ◽  
Transformation Kinetics ◽  
Cooling Process ◽  
Scanning Calorimetry ◽  
Kinetics Of

The temperature and duration of β1→α+β2 transformation of Ti-6Al-4V alloy in cooling process were measured by differential scanning calorimetry, and transformation activation energy and Avrami exponent of β1→α+β2 were also calculated. The results show that the cooling rate is in the range of 在5～20°C/min, the transformation temperature and the transformation duration β1→α+β2 transformation of Ti-6Al-4V alloy decreased with the increasing cooling rate, its transformation activation energy decreased with the increasing phase transformation volume fraction, and Avrami exponent was between 1 and 2 at 660°C.

Non—Isothermal Differential Scanning Calorimetry Studies on Nanocrystallization Kinetics of Fe81Si3.5B13.5C2 Amorphous Alloy

2011 ◽  
Vol 688 ◽  
pp. 180-185
Author(s):  
Yu Zhang ◽  
Wei Lu ◽  
Biao Yan ◽  
Yu Xin Wang ◽  
Ying Yang
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Amorphous Alloy ◽  
Three Dimensional ◽  
Crystallization Mechanism ◽  
Scanning Calorimetry ◽  
Average Value ◽  
Initial Stage ◽  
Friedman Method ◽  
Kinetics Of

The nanocrystallization kinetics of the Fe81Si3.5B13.5C2amorphous alloy was investigated by differential scanning calorimetry (DSC). The apparent activation energy Ea, as well as the nucleation and growth kinetic parameters has been calculated by Kissinger and Ozawa methods. The changeable activation energy Eawith crystalline fraction α was obtained by the expended Friedman method without assuming the kinetic model function, and the average value of Eawas 364±20 kJ/mol. It was shown that the crystallization mechanism of initial stage (0<α<0.7) of the transformation was bulk crystallization with two and three dimensional nucleation graining growth which was controlled by diffusion. For the middle stage (0.7<α<0.9), the crystallization mechanism is surface crystallization with one dimensional nucleation graining growth at a near-zero nucleation rate. In the final stage(α>0.9)，the local Avrami exponents rose anomalously from 1.4 to about 2.0.

scholarly journals Application of the Shrinking-Core Models for Determination of Dissolution Kinetics of Mn and Zn from Spent Zinc–Carbon Battery Powder in Organic Acid Solution

2019 ◽  
Vol 27 (1) ◽  
pp. 99-109 ◽  
Author(s):  
Tevfik Agacayak ◽  
Hasan Ali Taner
Keyword(s):  
Acetic Acid ◽  
Acid Solution ◽  
Acetic Acid Solution ◽  
Dissolution Kinetics ◽  
Kinetic Studies ◽  
Product Layer ◽  
Different Temperatures ◽  
Shrinking Core ◽  
Kinetics Of Dissolution ◽  
Kinetics Of

Abstract In this study, dissolution kinetics of manganese and zinc from spent zinc–carbon batteries in acetic acid solution was investigated. To determine the kinetics of dissolution of manganese and zinc, shrinking core model was applied to dissolution recoveries obtained at different temperatures. As a result of kinetic studies, it was determined that manganese and zinc were dissolved in acetic acid solution by diffusion from product layer and then activation energies (Ea) were calculated.

scholarly journals Kissinger Method in Kinetics of Materials: Things to Beware and Be Aware of

Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2813 ◽  
Author(s):  
Sergey Vyazovkin
Keyword(s):  
Activation Energy ◽  
Isoconversional Methods ◽  
Single Step ◽  
Order Reaction ◽  
Kissinger Method ◽  
Scanning Calorimetry ◽  
First Order ◽  
Kinetics Of ◽  
Final Equation ◽  
Derivative Thermogravimetry

The Kissinger method is an overwhelmingly popular way of estimating the activation energy of thermally stimulated processes studied by differential scanning calorimetry (DSC), differential thermal analysis (DTA), and derivative thermogravimetry (DTG). The simplicity of its use is offset considerably by the number of problems that result from underlying assumptions. The assumption of a first-order reaction introduces a certain evaluation error that may become very large when applying temperature programs other than linear heating. The assumption of heating is embedded in the final equation that makes the method inapplicable to any data obtained on cooling. The method yields a single activation energy in agreement with the assumption of single-step kinetics that creates a problem with the majority of applications. This is illustrated by applying the Kissinger method to some chemical reactions, crystallization, glass transition, and melting. In the cases when the isoconversional activation energy varies significantly, the Kissinger plots tend to be almost perfectly linear that means the method fails to detect the inherent complexity of the processes. It is stressed that the Kissinger method is never the best choice when one is looking for insights into the processes kinetics. Comparably simple isoconversional methods offer an insightful alternative.

Thermal Reaction Kinetics of Fly Ash Cement Paste at the Age of 28 Days

2014 ◽  
Vol 668-669 ◽  
pp. 91-94 ◽  
Author(s):  
Xiao Fang He ◽  
Chang Wen Miao ◽  
Yong Hao Wu ◽  
Xin Xin Cao ◽  
Dan Liu
Keyword(s):  
Activation Energy ◽  
Fly Ash ◽  
Apparent Activation Energy ◽  
Reaction Kinetics ◽  
Thermal Reaction ◽  
Physical Parameters ◽  
Scanning Calorimetry ◽  
Kinetics Parameters ◽  
Cement Pastes ◽  
Kinetics Of

The thermal reaction kinetics of fly ash cement pastes were studied by Differential Scanning Calorimetry (DSC) and Thermal Gravity Analysis-Differential Thermal Gravity (TG-DTG) method, the kinetics parameters such as apparent activation energy was calculated by the Kissinger method, and the physical parameters were obtained. The result show that the fly ash cement pastes performance three endothermic reaction stages at different heating rates, peak temperatures of each stage at the range of 91.85~121.08°C, 453.93~496.48°C, and 680.21~751.62°C. TG-DTG show there were three thermal decomposition stages, thermal dehydration reaction apparent activation energy of fly ash cement pastes in each stage were 47.23kJ/mol, 128.84kJ/mol, and 134.07kJ/mol.

Dissolution kinetics of Amazonian metakaolin in hydrochloric acid

Clay Minerals ◽  
2017 ◽  
Vol 52 (1) ◽  
pp. 75-82 ◽  
Author(s):  
Paula E.A. Lima ◽  
Rômulo S. Angélica ◽  
Roberto F. Neves
Keyword(s):  
Hydrochloric Acid ◽  
Dissolution Kinetics ◽  
Regression Coefficients ◽  
Shrinking Core Model ◽  
First Order ◽  
Constant Size ◽  
Shrinking Core ◽  
Kinetics Of Dissolution ◽  
Leaching Reaction ◽  
Kinetics Of

AbstractThe kinetics of dissolution of Amazonian metakaolin in hydrochloric acid (HCl) was studied using the ‘Shrinking Core Model’ for spherical and ‘flat plate’ particles of constant size. The Amazonian kaolin was calcined at 700°C for 2 h. The calcined samples (metakaolins) were leached in an HCl solution with 5% excess at 70, 80 and 95 ± 3°C for 3 h. Samples were collected every 15 min and subjected to Al analysis by the EDTA titrimetric method. Experimental data showed that the spherical morphology produced a better fit with respect to the regression coefficients. The activation energy of the reaction was 90.6 kJ/mol. The chemical process is a first-order leaching reaction. The results of the present study are consistent with those from previous research on this topic, which used HCl with an excess of >90%.

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