• 마이크로전자및패키징학회지
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• 제24권1호
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• pp.67-73
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• 2017

열중량 분석(Thermogravimetry)을 이용하여 열화시간 경과에 따른 접착 소재의 열에 대한 열화 특성을 분석하였다. 실험에는 여섯 가지의 온도 승온률에서 측정된 데이터를 이용하여 열화에 따른 동적 반응을 분석하였다. 이 데이터를 바탕으로 아레니우스 방정식을 이용하여 활성 에너지와 비례 상수 등 모델에 필요한 계수를 계산하였다. 또한 열화거동을 예측하는 방정식으로는 무게 감소에 따른 간단한 n차 방정식을 이용하였다. 구해진 예측 모델은 실험 데이터와 비교하여 검증하였다. 계산 결과 각 승온률에 따라 활성화 에너지의 크기가 다름에 따라 평균값을 사용하여 계산한 결과는 낮은 승온률인 경우에는 잘 예측하였지만 높은 승온률인 경우에는 측정값과 차이를 보였다. 이와 같은 문제를 해결하기 위해 지수함수 급수를 이용한 새로운 모델링 방법이 처음 시도되었으며 예측된 결과는 승온률에 관계없이 실험 데이터와 잘 일치하였다.

• 폴리머
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• 제24권6호
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• pp.777-786
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• 2000

본 연구에서는 범용 열가소성 수지인 폴리프로필렌 (virgin polypropylene, VPP)과 폴리프로필렌을 주성분으로 하는 재생플라스틱의 난연성을 향상시키기 위하여, 난연제 decabromodiphenyl oxide (DBDPO)와 chlorinated paraffin wax (CPW)를 혼합하여 이것들의 난연 특성을 정량적으로 비교 분석 연구하였다. 난연성 평가 측정으로 콘 칼로리미터 (cone calorimeter, ASTM E1354, ISO 5660), 한계산소지수 측정 (LOI, ASTM D2863, ISO 4589) 등을 사용하였고, 콘 칼로리미터를 이용하여 DBDPO와 CPW의 난연효율을 정량적으로 측정하였다. 콘 칼로리미터의 결과로 난연제의 난연효율을 측정한 결과, DBDPO가 CPW보다는 약 2배의 난연효율을 가지고 있다는 것을 확인하였고, 한계산소지수 측정 결과와 유사한 난연효율을 보임을 확인하였다. 열중량 분석 (TGA) 측정결과 난연제 DBDPO를 첨가하였을 때 약 30~5$0^{\circ}C$의 열분해 온도의 상승을 확인할 수 있었다.

• Current Research on Agriculture and Life Sciences
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• 제31권1호
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• pp.18-24
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• 2013

This work attempted to fabricate organic/inorganic nanocomposite by combining organic cellulose nanofibrils (CNFs), isolated by 2,2,6,6-tetramethylpiperidine-1-oxy radical (TEMPO)-mediated oxidation of native cellulose with inorganic nanoclay. The morphology and dimension of CNFs, and tensile properties and thermal stability of CNF/clay nanocomposites were characterized by transmission electron microscope (TEM), tensile test, and thermogravimetry (TG), respectively. TEM observation showed that CNFs were fibrillated structure with a diameter of about $4.86{\pm}1.341nm$. Tensile strength and modulus of the hybrid nanocomposite decreased as the clay content of the nanocomposite increased, indicating a poor dispersion of CNFs or inefficient stress transfer between the CNFs and clay. The elongation at break increased at 1% clay level and then continuously decreased as the clay content increased, suggesting increased brittleness. Analysis of TG and derivative thermogravimetry (DTG) curves of the nanocomposites identified two thermal degradation peak temperatures ($T_{p1}$ and $T_{p2}$), which suggested thermal decomposition of the nanocomposites to be a two steps-process. We think that $T_{p1}$ values from $219.6^{\circ}C$ to $235^{\circ}C$ resulted from the sodium carboxylate groups in the CNFs, and that $T_{p2}$ values from $267^{\circ}C$ to $273.5^{\circ}C$ were mainly responsible for the thermal decomposition of crystalline cellulose in the nanocomposite. An increase in the clay level of the CNF/clay nanocomposite predominately affected $T_{p2}$ values, which continuously increased as the clay content increased. These results indicate that the addition of clay improved thermal stability of the CNF/clay nanocomposite but at the expense of nanocomposite's tensile properties.

• 자원리싸이클링
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• 제9권5호
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• pp.11-15
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• 2000

The sample made of $Mn_3O_4$ indicated an excellent frequency dependency for intial permeability and core loss. Moreover the homogeneity of cation configuration in he spinel structure was confirmed by X-ray diffraction analysis. The result of homogeneity of the spinel structural coincided with the analytical results of temperature dependence of magnetization. Furthermore, the influence of manganese oxide as starting material, on homogeneity of spinel structure was examined by using thermogravimetry-differential thermal analysis. It may be concluded that the reaction between $Mn_3O_4$ and Fe-Zn oxide mixture proceeds at fist in all combination of manganese oxide and oxie mixture, and then Mn-Zn-Fe spinel was formed.

• Carbon letters
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• 제8권1호
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• pp.17-24
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• 2007

Microporous carbons with narrow pore size distribution have been successfully synthesized by using hydrolyzed and calcined silica as templates and phenol formaldehyde (pf) resin as carbon precursor. Phenol formaldehyde-silica micro composites were prepared by solution route. Subsesequently, silica templates were removed by HF leaching. Resulting carbons were steam activated. The porous carbons were characterized by nitrogen adsorption-desorption isotherm, SEM, FTIR analysis, iodine adsorption, thermogravimetry analysis, etc. Adsorption isotherms show that the porous carbon prepared from calcined silica as templates are microporous with 88% pores of size <2 nm porosity and are of type I isotherm, while porous carbon prepared by using hydrolyzed silica are microporous with 89% microporosity, shows hysteresis loop at high relative pressure indicating the presence of some mesoporosity in samples. The microporosity in porous carbon materials has a bearing on the nature of silica templates used for pore formation.

• 분석과학
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• 제16권2호
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• pp.117-124
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• 2003

고온 건식공정의 사용후핵연료 산화분말 ($U_3O_8$)과 경 중수로 연계 핵연료 제조공정의 $UO_2$ 소결체 물성 이해에 필요한 Oxygen/Metal 비를 습식 및 건식 분석방법으로 측정하였다. $UO_2$ 분말에 핵분열생성물 원소의 산화물을 일정량 첨가하고 $1,700^{\circ}C$의 수소분위기에서 소결시켜 20,000~60,000 MWd/MtU 연소도 범위의 사용후핵연료와 화학조성이 유사한 모의 사용후핵연료를 제조하였다. 습식법에 의한 O/M 비 측정을 위하여 혼합산 (10 M HCl : 8 M $HNO_3$, 2.5:1 V/V)에 의한 가압산분해법으로 모의 사용후핵연료를 용해하고 우라늄과 핵분열생성물 원소를 추출 크로마토그래피로 분리한 후 금속원소의 총량을 유도결합플라스마 원자방출분광분석법으로 결정하였다. 또한 $UO_2$가 산화될 때의 무게변화를 열중량 무게분석법 (thermogravimetric)으로 측정하여 O/M비를 계산하고 습식법으로 얻은 결과와 비교하였다. $Mo_{0.4}-Ru_{0.4}-Rh_{0.1}-Pd_{0.1}$ 합금이 O/M비 측정에 미치는 영향을 조사하였다.

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2008년도 제38차 학술발표대회
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• pp.114-116
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• 2008

Poly(${\varepsilon}$-caprolactone) nanocapsules(nanoPCL) containing phytoncide oil were synthesized by emulsion diffusion method using ethyl acetate as organic solvent. The influence of the degree of hydrolyzation of poly(vinyl acohol) used as an emulsion stabilizer, and the different weight ratio of core material to wall material on the particle size, morphology, and emulsion stability was investigated to design nanocapsules. The encapsulated nanoPCL were characterized by FT-IR spetrometry, Scanning electron microscope, Differential scanning calorimetry, and Thermogravimetry analysis, respectively.

• 한국전기화학회:학술대회논문집
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• 한국전기화학회 2005년도 수소연료전지공동심포지움 2005논문집
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• pp.373-378
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• 2005

[ $Zn(BH_4)_2$ ] ($8.4\;wt\%$ theoretical hydrogen storage capacity) powders have been successfully synthesized by mechanochemical reaction from mixtures of $ZnCl_2$ and $NaBH_4$ powders in a 1:2 molar ratio in different times. $$ZnCl_2\;+\;2NaBH_4\rightarrow\;Zn(BH_4)_2\;+\;2NaCl\;(1)$$ $Zn(BH_4)_2$ powders were characterized by X-ray diffractometry(XRD), and Furier Transform Infrared spectrometry(FT-IR). The thermal stabilities of $Zn(BH_4)_2$ powders were studied by Differential scanning calorimetry(DSC), Thermogravimetry analysis(TGA), and Mass spectrometry(MS). $Zn(BH_4)_2$ can be tested for hydrogen evolution without further purification. The reaction to yield hydrogen is irreversible, the other products being compounds of Zn, and borane. $Zn(BH_4)_2$ thermally decomposes to release borane and hydrogen gas between about 85 and $150^{\circ}C$.

• 한국산업융합학회 논문집
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• 제9권1호
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• pp.45-50
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• 2006

In order to analyse the properties of the fiber-adhesive that was used as Flocking process we synthesized quaterpolymer with the variation of the types of monomer ratio by emulsion polymerization. We characterized the properties of this adhesive: Differential Scanning Calorimeter(DSC), Thermogravimetry Analysis(TGA), Raman spectroscopy. The polymer was synthesized by changing the using amount of 2-EHAM, and then we investigated the characteristics of glass transition temperature(Tg), melting temperature(Tm), thermal stability and hydroxyl group respectively. The optimum monomer composition was 36.84% EAM, 15.79% MAM, 42.1% 2-EHAM and 5.26% AAc.

• 한국세라믹학회지
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• 제27권3호
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• pp.383-388
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• 1990

Hydraulic properties of CA2-based clinker synthesized by Hydration-Burning Method was studied by calorimetry, analysis of suspension, thermogravimetry, scanning electron microscopy and X-ray diffractometry. Hydraulic properties of the clinker was so activated that heat of hydration of the clinker evolved faster than that of CA synthesized by conventional method. In suspension of W/C=33, dissolution of the clinker began at nearly same time as that of CA, but precipitation of AH3 and rise of [OH-] occurred fairly faster in the suspension of the clinker than that of CA. From the beginning of hydration, AH3 was produced and became a main phase of the hydrate with minor phase of CAH10 and C2AH8, but C3AH6 was not produced at ambient temperature.