• Title/Summary/Keyword: 열분해 활성화 에너지

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Thermal Decomposition Energy of Liquid Crystalline Epoxy (열경화성 액정 에폭시 수지의 열분해 활성화에너지)

  • Seung Hyun Cho
    • Composites Research
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    • v.37 no.1
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    • pp.1-6
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    • 2024
  • A liquid crystalline thermosetting epoxy was synthesizes with DGE-DHMS and 1-Methyl Imidazole. To investigate thermal stability, activation energies for thermal decomposition were calculated via Flynn-Wall-Ozawa method and Kissinger method with the data obtained from TGA analysis. The result showed that there were no differences in thermal decomposition behavior between liquid crystalline phases and isotropic phase and also the same thermal decomposition mechanism was applied to the entire process.

Thermal Decomposition Activation Energy of Liquid Crystalline Epoxy using Cationic Initiator (양이온 개시제를 이용한 열경화성 액정 에폭시의 열분해 활성화에너지)

  • Jung, Ye Ji;Hyun, Ha Nuel;Cho, Seung Hyun
    • Composites Research
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    • v.34 no.3
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    • pp.180-185
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    • 2021
  • Due to the formation of random three dimensional network structure, which cause a lot of scattering of phonons, the thermal conductivity is low when the liquid crystalline epoxy is cured with amine-based curing agent. This problem is solved by using a cationic initiator that can make mesogen groups to be stacked structure. In this experiment, the thermal stability is compared by investigating the activation energy of isothermal decomposition through TGA of an epoxy using an amine-based curing agent and a cationic initiator. As a result, the energy of the activation of the epoxy using a cationic initiator is high. Compared with the previous experiments, the thermal stability is similar to the thermal conductivity.

Thermal Degrndation of High Molecular Components obtained from Kiln Pyrolysis Reactor (킬른 열분해 반응기로부터 생성된 고분자량 성분의 열적분해)

  • Oh, Sea-Cheon;Ryu, Jae-Hun;Kwak, Hyun;Bae, Seong-Youl;Lee, Kyung-Hwan;Liu, Daivd
    • 한국신재생에너지학회:학술대회논문집
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    • 2007.11a
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    • pp.623-626
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    • 2007
  • 킬른형 열분해 반응기를 이용하여 혼합폐플라스틱의 열분해로부터 얻어진 고분자성분의 열적분해 특성에 관한 연구를 TGA와 GC-MS를 이용하여 수행하였다. 열적분해의 속도론적 연구는 $10{\sim}50^{\circ}C/min$ 사이의 여러 가열속도에서 비등온 질량감소 기술을 이용하여 수행하였으며 활성화 에너지 및 반응 차수와 같은 속도 상수들에 대한 정보를 얻기 위하여 문헌에 제시된 여러 가지의 속도론 해석방법을 이용하여 질량감소곡선 및 그 미분 값을 해석하였다. 또한 회분식 열분해 반응기를 이용하여 반응온도에 따른 액상 생성물의 수율변화를 고찰하였으며 GC-MS를 이용하여 액상 생성물의 반응온도 증가에 따른 특성연구를 수행하였다.

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Investigation of the Adsorption Properties of Activated Carbon Made by Chemical Activation of Mixed Waste Plastic Pyrolysis Residues (혼합 폐플라스틱 열분해 잔류물의 화학적 활성화를 통해 제조한 활성탄의 흡착 특성 조사)

  • Eun-Jin Moon;Yunsuk Kang;Byoungsun Park
    • Journal of the Korean Recycled Construction Resources Institute
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    • v.11 no.4
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    • pp.391-399
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    • 2023
  • Recently, low-temperature pyrolysis technology has been studied as a recycling method for waste plastic. Low-temperature pyrolysis technology for waste plastic produces pyrolysis oil that can be used as an energy resource, but solid residue remains. Waste plastic pyrolysis residues are mostly landfilled due to their limited use. In this study, it is investigated that mixed waste plastic pyrolysis residues could be recycled into activated carbon. It was confirmed that the fixed carbon content of the residue was 33.69 % from proximate Analysis. Chemical activation was used to manufacture activated carbon. KOH was used as an activator. To investigate the effect of the mixing ratio of KOH and residue, samples were mixed at ratios of 0.5, 1.0, and 2.0. The mixed sample was chemically activated at an activation temperature of 800 ℃ for 1 hour. As a result of analyzing the characteristics of activated carbon through BET, it was confirmed that the specific surface area increased as the mixing ratio of KOH increased.

A Study on Thermal Stability of Chlorinated Polyethylene (함염소 폴리에틸렌의 열안정성에 관한 연구)

  • Seul S. D.;Lee N. W.
    • Journal of the Korean Institute of Gas
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    • v.1 no.1
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    • pp.120-126
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    • 1997
  • The thermal decomposition of low density polyethylene(LDPE) and $25\%{\~}48\%$ chlorinated polyethylene(CPE) were studied using a dynamic thermogravimetry in the stream of nitrogen gas with 20ml/min. The mathematic method, differential (Friedman) and Integral (Ozawa) method were used to obtain value of activation energy of decomposition energy on the reaction. The activation energies evaluated by the above methods agree with each other very well. The maximum average activation energy calculated was 71.71kcal/mol. The thermal decomposition of LDPE and CPE were considered to be carried out by main chain scission and the thermogravimetric trace curve agree with the theoretical equation.

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The distribution of activation energy and frequency factor for coal pyrolysis and char-air reaction (열분해 및 촤 - 공기 반응시의 활성화 에너지 및 빈도계수 분포)

  • Park, Ho-Young;Kim, Young-Joo
    • Journal of Energy Engineering
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    • v.18 no.1
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    • pp.9-16
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    • 2009
  • The experimental work has been carried out for the study of pyrolysis and char-air reaction of five coals used in Y power station in Korea. For five coals, the characteristics of pyrolyis and char reaction have been investigated with TGA, and their kinetic parameters were obtained and compared each other. The order of pyrolysis rate for five coals were as follows : Peabody, Flame, MIP, Indominco, Elk valley. The behavior of char - air reaction for five coal chars have been successfully described by the grain model. The rate of char-air reaction gave the maximum value for Flame coal char, on the while Elk valley coal char had the minimum value. For the reaction temperature over 1,000K, Flame coal char - air reaction was very fast compared with other coal chars.

Characteristics of low temperature pyrolysis of LDPE, PS, ABS plastics (저온열분해조건에서 LDPE, PS, ABS의 열분해생성물 생성특성)

  • Cha, Wang-Seog;Jang, Hyun-Tae
    • 한국신재생에너지학회:학술대회논문집
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    • 2008.05a
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    • pp.468-470
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    • 2008
  • 열중량반응기와 미분반응기를 이용하여 ABS의 열분해 및 생성물분포 특성을 연구하였으며 미분반응기를 이용한 실험의 열분해온도는 $410{\sim}450^{\circ}C$이었다. 각 상의 열분해생성물의 수율은 무게측정을 통해 얻었으며 액상생성물의 탄소수분포는 GC-SIMDIS 방법을 통해 측정하였다. 열중량 분석실험에서는 측정할 수 없었던 다량의 고상잔류물의 생성을 회분식 미분반응기실험을 통해 확인할 수 있었다. 반응온도와 시간이 증가할수록 액상생성물의 수율과 평균분자량은 감소하였으나 액상생성물 중의 스티렌모노머의 생성은 두드러지게 증가하였다. ABS 열분해 반응에서 말단절단의 속도계수인 활성화에너지 값은 54.1kcal/mole이었다.

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Preparation of Quaternary Energetic Composites by Crystallization and Their Thermal Decomposition Characteristics (결정화에 의한 4성분계 에너지 복합체 제조 및 열분해 특성)

  • Kim, Byoung-Soo;Kim, Jae-Kyeong;Ahn, Ik-Sung;Kim, Hyoun-Soo;Koo, Kee-Kahb
    • Applied Chemistry for Engineering
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    • v.30 no.2
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    • pp.178-185
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    • 2019
  • Three spherical quaternary composites composed of metal/metal oxide/high explosive/oxidizer were prepared by a crystallization/agglomeration process. From the characteristics of composites by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), the shortening of the decomposition zone of high explosives in the quaternary composite was observed, which may be attributed to the autocatalytic reaction caused by $ClO_2$ or HCl which are ammonium perchlorate (AP) degradation products. The activation energy analysis showed that the activation energy abruptly decreases at the end of the decomposition zone of high explosives, and it was considered to be caused by $HNO_2$ which is common in decomposition products of high explosives. The activation energy predicted from complex pyrolysis results by the distributed activation energy model (DAEM) showed much better in accuracy than those by model-fitting methods such as Kissinger-Akahira-Sunose and Flynn-Wall-Ozawa models.

Non-isothermal TGA Analysis on Thermal Degradation Kinetics of Modified-NR Rubber Composites (비등온 TGA에 의한 개질NR고무복합재료지 열분해 Kinetics에 관한 해석)

  • Oh, Jeong-Seok;Lee, Joon-Mann;Ahn, Won-Sool
    • Polymer(Korea)
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    • v.33 no.5
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    • pp.435-440
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    • 2009
  • Thermal degradation behavior of CR (chloroprene) -modified NR (natural rubber) compounds, having different sulfur/accelerator compositions, was studied by non-isothermal TGA method. Data were analyzed using both Kissinger and Flynn-Wall-Ozawa analysis to assess the activation energies. Activation energy obtained from Kissinger analysis was $147.0{\pm}2.0$ kJ/mol for all samples, showing little effect of sulfur/accelerator composition changes in the samples. On the other hand, activation energy from Flynn-Wall-Ozawa analysis exhibited much variations with conversion, showing average value of $211.6{\pm}19.0$ kJ/mol. From the results, it was considered that whole thermal degradation processes of the samples were composed of complex multiple step processes, of which reaction mechanisms were different from each other.

Study on the Pyrolysis Kinetics of Deasphalted Oil Using Thermogravimetric Analysis (열중량 분석법을 이용한 Deasphalted Oil의 열분해 특성 분석)

  • Shin, Sang Cheol;Lee, Jung Moo;Lee, Ki Bong;Jeon, Sang Goo;Na, Jeong Geol;Nho, Nam Sun
    • Korean Chemical Engineering Research
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    • v.50 no.3
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    • pp.391-397
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    • 2012
  • The depletion of conventional oil reserves and the increasing energy need in developing countries such as China and India result in exceeding oil demand over supply. As a solution of the problem, the efficient utilization of heavy oil has been receiving more and more interest. In order to utilize heavy oil, upgrading processes are required. Among the upgrading processes, thermal decomposition is thought to be relatively simple and economical. In this study, to understand basic characteristics of thermal decomposition of heavy oil, we conducted pyrolysis experiments of deasphalted oil (DAO) produced by a solvent deasphalting process. DAO is a mixture of many components and consists mainly of materials of carbon number 20~40. For the comparison with results of DAO pyrolysis, additional pyrolysis experiments with single materials of carbon number 30 ($C_{30}H_{62}$, $C_{30}H_{58}O_4S$, $C_{30}H_{63}O_3P$) were conducted. Pyrolysis experiments were carried out non-isothermally with variation of heating rate (10, 50, $100^{\circ}C$/min) in a thermogravimetric analyzer. Average pyrolysis activation energy determined by using Arrhenius method, Ingraham and Marrier method, and Coats and Redfern method was 72~99 kJ/mol. In the activation energy calculated by Ozawa-Flynn-Wall method, DAO had wider variation than other single materials.