• Fire Science and Engineering
• /
• v.18 no.4
• /
• pp.52-56
• /
• 2004

An experiment to examine the characteristics of pyrolysis of Methyl Ethyl Ketone Peroxide was conducted in an air-present environment, using TG-DTA. Decomposition starting temperature was decreased as the increase of 98% concentrated H₂SO₄ to the MEKPO and the maximum decomposition temperature of MEKPO was 116.8℃. The activated energy calculated from differential method of pure MEKPO, MEKPO with 1 wt%, 3wt%, and 5wt% of H₂SO₄ were 0.576㎉/mo1, 0.355㎉/㏖, 0.284㎉/㏖ and 0.258㎉/㏖ respectively.

• Elastomers and Composites
• /
• v.42 no.1
• /
• pp.47-54
• /
• 2007

Reaction kinetics of polyurethane elastomers (PU) were studied using dynamic DSC and TGA for three PU samples of general purpose (Sample A), high temperature cross-likable CASE purpose with MOCA (Sample B), and RT cross-likable CASE purpose grade (Sample C). From DSC results, sample with MOCA(Sample B) showed lower shift of peak temperature, while showing broader thermograms than those of general purpose grade (Sample A). On the other hand, RT cross-linkable PU grade (Sample C) showed an interesting double mode reaction patterns, i.e., a lower temperature reaction at about $70\;^{\circ}C$, and a higher temperature reaction in the range of $140{\sim}170\;^{\circ}C$, indicating that it requires 2-step reaction process in order to complete the reaction. Once the cross-linking reaction completed, however, TGA results showed that all the samples would be considered to have similar chemical structures, showing similar decomposition processes. Sample C, especially, had showed decomposition properties of both Sample A and Sample B. Formation activation energies calculated from Kissinger method showed 10.39, 65.85, 36.52(Low $T_p$) and 18.21(High $T_p$) kcal/mol, while decomposition activation energies were 31.94, 30.84, 24.16 kcal/mol, respectively.

• Journal of the Korean Society of Propulsion Engineers
• /
• v.3 no.4
• /
• pp.23-30
• /
• 1999

The thermal decomposition of phase stabilized ammonium nitrate(PSAN) was studied by means of thermogravimetric analysis(TGA). In this study, potassium nitrate and zinc oxide were used as the phase stabilizers in the range of contents from 0 wt.% to 8 wt.%. The kinetics and mechanism for the decomposition were evaluated using integral methods. It was found that the thermal kinetic parameters such as activation energy(I) and frequency factor(A) increase with the increase of the stabilizer contents, and the mechanism of decomposition also changes.

• Composites Research
• /
• v.35 no.2
• /
• pp.53-60
• /
• 2022

This study uses Diglycidyl ether of terephthalylidene-bis-(4-amino-3-methylphenol) (DGETAM), an amine hardener 4,4'-diaminodiphenylethane (DDE) and cationic catalyst N-benzylpyrazinium hexafluoroantimonate (BPH) to make epoxy film. For analysis, ¹H_NMR and FT-IR were used to verify proper synthesis, and the liquid crystallinity of DGETAM was checked using Differntial Scanning Calorimetry and Polarized Optical Microscopy. Thermal conductivity of the sample was measured using Laser Flash Apparatus. Thermal stability as well as thermal conductivity is important when used as a packaging material. Activated energy is the energy needed to generate a response, which can be used to estimate the energy required to maintain physical properties. It was obtained using the Arrhenius equation based on the data measured by isothermal decomposition using Thermogravimetric Analysis. Measurement of the thermal conductivity of epoxy films showed higher thermal conductivity when DDE was used, and it was found that thermal conductivity had an effect on thermal stability, given that it represented an activation energy similar to a film with BPH upon 5% decomposition.

• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.7 no.2
• /
• pp.324-333
• /
• 1997

Porous alumina specimens with 80~92% relative densities were prepared from ultrasonic spray pyrolyzed alumina Powders by sintering at $1600^{\circ}$~ $1700^{\circ}C$. The exaggerated grain growth appeared to high sintering temperature and long soaking time. The microstructural development during sintering was investigated using image analysis. In the study of grain growth kinetics for sintering for spray prolyzed alumina powder, the activation energy for normal grain growth was 386.77 kJ/mol.

• Journal of the Korean Society of Tobacco Science
• /
• v.5 no.2
• /
• pp.55-62
• /
• 1983

Four of non- isothermal methods evaluating kinetics have been studied by using differential scanning calorimetry (DSC) and thermogravimetry (TG) and applied for kinetics of the thermal decomposition of cellulose. It is concluded that the heating evolution methods with DSC and approximative methods with TC can lead to satisfactory kinetic analysis. Results calculating the reacting order and the activation energy of cellulose decomposition were 1/2 order and 42kcaB/mol, respectively.

• Journal of the Korean Chemical Society
• /
• v.31 no.6
• /
• pp.590-600
• /
• 1987

Silicone-containing polyamide-imides were prepared from bis(p-chlorocarbonylphenyl)diphenylsilane (BCCDPS), pyromellitic dianhydride(PMDA) and diamines. The thermal characteristics of the above polymers had been carefully studied using a thermogravimetric analyzer. The thermal stability of polymer was decreased with increasing contents of bis(p-carbonylphenyl)diphenylsilane units(BCDPS). The effect of diamine on thermal stability of polymer led benzidine > m-phenylenediamine> 4,4'-diaminodiphenyl ether > 4,4'-diaminodiphenyl sulfone. The activation energy of degradation of polymer obtained by Friedman method increased as the contents of BCDPS in the polymer decreased. The degradation temperature of polymers generally increased as the activation energy increased. The solubility of polymer increased as the content of BCDPS increased except polymers prepared with benzidine.

• Elastomers and Composites
• /
• v.48 no.2
• /
• pp.161-166
• /
• 2013

Thermal degradation behavior of chlorine cure-site ACM and carboxylic cure-site ACM rubbers was studied by non-isothermal TGA thermal analysis. Carboxylic cure-site ACM rubber exhibited comparatively more thermally stable than chlorine cure-site ACM, showing higher peak temperature, at which maximum reaction rate occurred. Activation energies from Kissinger method were calculated as 118.6 kJ/mol for the chlorine cure-site ACM and 105.5 kJ/mol for the carboxylic cure-site ACM, showing similar values from Flynn-Wall-Ozawa analysis over the conversion range of 0.1~0.2. From the analysis of the reaction order change, both samples seemed thermally decomposed through the multiple reaction mechanism as is the common rubber materials.

• Proceedings of the Korean Environmental Sciences Society Conference
• /
• 2008.11a
• /
• pp.488-490
• /
• 2008

등온 및 비등온 TGA 열분석을 이용하여 TTSP를 이용하여 실험적으로 Shift factor(Acceleration factor) ${\alpha}_T$를 구하고 이로부터 마스터 커브 (master curve)를 도출할 수 있었고, 실험에 사용된 개질된 NR고무재료는 Arrhenius식을 잘 따르는 것이 확인되었으며, 이로부터 TTSP에 의한 촉진시험 결과의 신빙성을 확인할 수 있었다. 한편, 등온 TGA 실험으로부터 얻은 활성화에너지는 37.70 kJ/mol인 반면, 비등온 TGA로부터 Kissinger plot에 의해 얻은 활성화에너지는 166.20 kJ/mol이었는데, 이는 저온과 고온에서 서로 다른 분해기구에 의해 중량 감소가 일어나기 때문인 것으로 생각 되었다.

• Korean Journal of Food Science and Technology
• /
• v.11 no.3
• /
• pp.171-175
• /
• 1979

Thermal properties of crude papain and crude peroxidase from domestic papaya were investigated. The crude extract of papaya was inactivated at the temperature range of $60^{\circ}{\sim}90^{\circ}C$ at pH 7.0 and the rest of the activities of papain and peroxidase were determined, respectively. The heat inactivation of papain and papaya peroxidase was biphasic at low temperature. For the thermal inactivation of papain extract, the enthalpy of activation was 91.4 kJ/mol, the entropy of activation, -49.6 J/mol K, and the free energy of activation, 108.5 kJ/mol. The activation energy for the inactivation of papaya peroxidase was 168.5 kJ/mol, the entropy of activation, $200.4\;J/mol{\cdot}K$ and the free energy of activation, 99.7 kJ/mol. The thermal stability of papain showed that it has a possibility for use as a meat tenderizer. It was also discussed that papaya peroxidase could be more suitable as a biochemical criteria for heat treatment than papaya catalase.