• Title/Summary/Keyword: Thermogravimetric Analysis

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탄소섬유 산화 현상을 고려한 탄소복합재료의 섬유체적비 측정법 (Method for Determining Fiber Volume Fraction in Carbon/Epoxy Composites Considering Oxidation of Carbon Fiber)

  • 김윤호;;최충현;김천곤;김선원;임재혁
    • Composites Research
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    • 제28권5호
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    • pp.311-315
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    • 2015
  • 섬유체적비에 따라 복합재료의 기계적 열적 특성이 크게 달라지기 때문에, 복합재료 설계시 섬유체적비를 올바르게 측정하는 것이 매우 중요하다. 일반적으로 섬유체적비를 측정하는 여러 방법은 산화되지 않는 유리섬유나 세라믹섬유를 사용한 복합재료의 경우에는 적합하고 효율적이다. 하지만 산화현상이 있는 탄소섬유의 경우에는 산화 방법과 조건에 따라서 다른 결과를 가져오게 되며 그러므로 올바른 섬유체적비를 측정이 어렵다. 본 연구에서는 Thermogravimetric analysis를 수행하여 산화되는 탄소섬유의 질량 감소량을 보정하여 탄소섬유 복합재료의 섬유체적비를 측정하였고 현미경 단면 이미지를 이용하여 그 결과를 검증하였다.

혼합폐플라스틱의 열분해로부터 생성된 고분자성분의 열적분해 (Thermal Degradation of High Molecular Components Obtained from Pyrolysis of Mixed Waste Plastics)

  • 오세천;류재훈;곽현;배성열;이경환
    • 공업화학
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    • 제19권2호
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    • pp.191-198
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    • 2008
  • 혼합폐플라스틱의 열분해로부터 얻어진 고분자성분의 열적분해 특성에 대한 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 반응차수 등과 같은 속도 상수들에 대한 정보를 얻기 위하여 문헌에 제시된 여러 가지의 속도론 해석 방법을 이용하여 질량감소 곡선 및 그 미분 값을 해석하였다. 또한 회분식 열분해 반응기를 이용하여 반응온도 및 반응시간에 따른 액상 생성물의 수율변화를 고찰하였으며 GC-MS를 이용하여 반응온도의 증가에 따른 액상 생성물의 특성연구를 수행하였다.

삭마용 내열 복합재료의 열분해 반응인자 결정 (Determination of Thermal Decomposition Parameters for Ablative Composite Materials)

  • 김연철
    • 한국추진공학회:학술대회논문집
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    • 한국추진공학회 2005년도 제25회 추계학술대회논문집
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    • pp.22-25
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    • 2005
  • 열용량분석기(TGA)를 사용하여 고온에서의 탄소/페놀릭 복합재료의 열분해를 연구하였다. 온도상승 속도는 5, 10, 15, 30 그리고 $50^{\circ}C/min$ 이었으며 온도 상승속도가 증가할수록 최대 열분해 반응의 온도도 상승하였다. 열분해반응에서 얻어진 자료를 근간으로 물리-수학적인 모델을 제시하였으며 모델의 실효성을 판단하기 위하여 고체 추진기관 노즐의 연소시험을 통하여 내부 온도 분포 및 밀도 분포 자료를 해석 모델과 비교하였다. 향후 연구를 통하여 이러한 열분해 인자는 고체 추진기관의 열 및 구조 해석의 입력 자료로 활용이 될 것이다.

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Thermal Behavior of Hwangto and Wood Flour Reinforced High Density Polyethylene (HDPE) Composites

  • Lee, Sun-Young;Doh, Geum-Hyun;Kang, In-Aeh
    • Journal of the Korean Wood Science and Technology
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    • 제34권5호
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    • pp.59-66
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    • 2006
  • The thermal properties of wood flour, Hwangto, and maleated polyethylene (MAPE) reinforced HDPE composites were investigated in this study. The thermal behavior of reinforced wood polymer composites was characterized by means of thermogravimetric (TGA) and differential scanning calorimetric (DSC) analyses. Hwangto and MAPE were used as an inorganic filler and a coupling agent, respectively. According to TGA analysis, the increase of wood flour level increased the thermal degradation of composites in the early stage, but decreased in the late stage. On the other hand, Hwangto reinforced composites showed the higher thermal stability than virgin HDPE, from the determination of differential peak temperature ($DT_p$). Decomposition temperature of wood flour and/or Hwangto reinforced composites increased with increase of heating rate. From DSC analysis, melting temperature of reinforced composites little bit increased with the addition of wood flour or Hwangto. As the loading of wood flour or Hwangto to HDPE increased, overall enthalpy decreased. It showed that wood flour and Hwangto absorbed more heat energy for melting the reinforced composites. Hwangto reinforced composites required more heat energy than wood flour reinforced composites and virgin HDPE. Coupling agent gave no significant effect on the thermal properties of composites. Thermal analyses indicate that composites with Hwangto are more thermally stable than those without Hwangto.

Influence of Sample Preparation on Thermogravimetric Analysis of Poly(Ethylene-co-Vinyl Acetate)

  • Lee, Sang-jin;Choi, Sung-Seen
    • Elastomers and Composites
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    • 제51권3호
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    • pp.206-211
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    • 2016
  • Experimental error sources for thermogravimetric analysis (TGA) of poly(ethylene-co-vinyl acetate) (EVA) were investigated and sample preparation method to reduce the experimental error was suggested. Maximum dissociation temperatures of EVA for the first and second dissociation reactions ($T_{m1}$ and $T_{m2}$, respectively) were measured. By decreasing the weight of raw EVA, the $T_{m1}$ increased but the the $T_{m2}$ decreased. When weight of the raw EVA was over 10 mg, the TGA curve showed abnormal behaviors. The abnormal TG behaviors were explained by gathering and instantaneous evaporation of acetic acid formed by deacetylation of the VA unit. When TGA analysis of EVA was performed using untreated (raw) EVA, the experimental errors were about 1%. In order to eliminate the abnormal TG behaviors and to reduce the experimental errors, EVA film made by solvent casting was used. For the treated EVA (EVA film), the abnormal TG behaviors did not appear, the $T_{m1}$ decreased by about $2^{\circ}C$ but the $T_{m2}$ increased by about $6^{\circ}C$, and the experimental errors were reduced by 0.5%.

Mechanical and Thermal Properties of Polypropylene/Wax/MAPP Composites Reinforced with High Loading of Wood Flour

  • Lee, Sun-Young;Kang, In-Aeh;Doh, Geum-Hyun;Mohan, D. Jagan
    • 한국응용과학기술학회지
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    • 제24권4호
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    • pp.416-426
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    • 2007
  • Polypropylene (PP) composites with wood flour/wax/coupling agent were manufactured by melt compounding and injection molding. The influence of wood flour(WF), wax, and coupling agent on the mechanical and thermal properties of the composites was investigated. The addition of wood flour to neat PP has the higher tensile modulus and strength compared with neat PP. The presence of wax also improved the tensile modulus. At the same loading of PP and WF, the addition of coupling agent highly decreased the tensile modulus, and increased the tensile strength. From thermogravimetric analysis (TGA), the addition of wax improved the thermal stability of the composites in the later stages of degradation. The presence of MAPP and wood flour in turn decreased thermal stabilities of composites. From differential scanning calorimetry analysis (DSC), neither the loading of wax. nor the presence of MAPP has shown significant effect on the thermal transition of composites.

Thermal Degradation Kinetics of Antimicrobial Agent, Poly(hexamethylene guanidine) Phosphate

  • Lee, Sang-Mook;Jin, Byung-Suk;Lee, Jae-Wook
    • Macromolecular Research
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    • 제14권5호
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    • pp.491-498
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    • 2006
  • The thermal degradation of poly(hexamethylene guanidine) phosphate (PHMG) was studied by dynamic thermogravimetric analysis (TGA) and pyrolysis-GC/MS (p-GC). Thermal degradation of PHMG occurs in three different processes, such as dephosphorylation, sublimation/vaporization of amine compounds and decomposition/ recombination of hydrocarbon residues. The kinetic parameters of each stage were calculated from the Kissinger, Friedman and Flynn-Wall-Ozawa methods. The Chang method was also used for comparison study. To investigate the degradation mechanisms of the three different stages, the Coats-Redfern and the Phadnis-Deshpande methods were employed. The probable degradation mechanism for the first stage was a nucleation and growth mechanism, $A_n$ type. However, a power law and a diffusion mechanism, $D_n$ type, were operated for the second degradation stage, whereas a nucleation and growth mechanism, $A_n$ type, were operated again for the third degradation stage of PHMG. The theoretical weight loss against temperature curves, calculated by the estimated kinetic parameters, well fit the experimental data, thereby confirming the validity of the analysis method used in this work. The life-time predicted from the kinetic equation is a valuable guide for the thermal processing of PHMG.

Thermal Decomposition Behavior and Durability Evaluation of Thermotropic Liquid Crystalline Polymers

  • Shin, Sang-Mi;Kim, Seong-Hun;Song, Jun-Kwang
    • Macromolecular Research
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    • 제17권3호
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    • pp.149-155
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    • 2009
  • The thermal decomposition behavior and degradation characteristics off our different thermotropic liquid crystalline polymers (TLCPs) were studied. The thermal decomposition behavior was determined by means of thermogravimetric analysis (TGA) at different heating rates in nitrogen and air. The order of the thermal stability was as follows: multi-aromatic polyester > hydroxybenzoic acid (HBA)/hydroxynaphthoic acid (HNA) copolyester > HNA/hydroxyl acetaniline (HAA)/terephthalic acid (TA) copolyester > HBA/Poly(ethylene terephthalate) (PET) copolyester. The activation energies of the thermal degradation were calculated by four multiple heating rate methods: Flynn-Wall, Friedman, Kissinger, and Kim-Park. The Flynn-Wall and Kim-Park methods were the most suitable methods to calculate the activation energy. Samples were exposed to an accelerated degradation test (ADT), under fixed conditions of heat ($63{\pm}3^{\circ}C$), humidity ($30{\pm}4%$) and Xenon arc radiation ($1.10\;W/m^2$), and the changes in surface morphology and color difference with time were determined. The TLCPs decomposed, discolored and cracked upon exposure to ultraviolet radiation.

Bio-oil production using residual sewage sludge after lipid and carbohydrate extraction

  • Supaporn, Pansuwan;Ly, Hoang Vu;Kim, Seung-Soo;Yeom, Sung Ho
    • Environmental Engineering Research
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    • 제24권2호
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    • pp.202-210
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    • 2019
  • In order to maximize the utilization of sewage sludge, a waste from wastewater treatment facility, the residual sewage sludge generated after lipid and carbohydrate extraction for biodiesel and bioethanol production was used to produce bio-oil by pyrolysis. Thermogravimetric analysis showed that sludge pyrolysis mainly occurred between 200 and $550^{\circ}C$ (with peaks formed around 337.0 and $379.3^{\circ}C$) with the decomposition of the main components (carbohydrate, lipid, and protein). Bio-oil was produced using a micro-tubing reactor, and its yield (wt%, g-bio-oil/g-residual sewage sludge) increased with an increase in the reaction temperature and time. The maximum bio-oil yield of 33.3% was obtained after pyrolysis at $390^{\circ}C$ for 5 min, where the largest amount of energy was introduced into the reactor to break the bonds of organic compounds in the sludge. The main components of bio-oil were found to be trans-2-pentenoic acid and 2-methyl-2-pentenoic acid with the highest selectivity of 28.4% and 12.3%, respectively. The kinetic rate constants indicated that the predominant reaction pathway was sewage sludge to bio-oil ($0.1054min^{-1}$), and subsequently to gas ($0.0541min^{-1}$), rather than the direct conversion of sewage sludge to gas ($0.0318min^{-1}$).

TGA를 이용한 Chlorinated Poly Vinyl Chloride(CPVC)의 활성화 에너지 평가 (Evaluation of the Activation Energy of Chlorinated Poly Vinyl Chloride (CPVC) Using Thermogravimetric Analysis)

  • 박형주
    • 한국화재소방학회논문지
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    • 제33권1호
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    • pp.1-6
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    • 2019
  • 열중량 분석법(TGA)을 이용하여 소방용 합성수지 배관으로 사용되는 CPVC의 활성화 에너지를 측정하였다. 열중량 분석법을 이용한 활성화 에너지는 Kissinger method와 Flynn-Wall-Ozawa method를 이용하여 계산하였다. 활성화 에너지를 계산한 결과 Kissinger method에 의해 128.07 kJ/mol, Flynn-Wall-Ozawa method에 의해 145.60 kJ/mol로 나타났다. Kissinger method와 Flynn-Wall-Ozawa method에 의해 계산된 활성화 에너지의 차이는 해석 방법이 다르다는 점을 감안했을 때 큰 차이가 없다고 판단된다. 향후 가속열화을 이용한 열적 열화평가 및 공기오븐노화시험을 통한 CPVC의 연소특성을 시험하고, 수명을 예측하고자 한다.