• Journal of Magnetics
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• 제6권1호
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• pp.23-26
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• 2001

Nano-crystalline hexaferrite $BaFe_{12}O_{19}$(BaM) thin films have been prepared by the sol-gel method. A solution of Ba-nitrate and Fe-nitrates was dissolved in solvent with the stoichiometric ratio Ba/Fe=1/10. Films were spin-coated onto $SiO_2$Si substrates, dried and then heated in air at various temperatures. In films prepared at a drying temperature $T_d=250^{\circ}C$ and a crystallizing temperature 650${\circ}C$, single-phase BaM was obtained. High coercivities were obtained in these nano-crystalline thin films, 4~5.5 kOe for hexaferrite. Polycrystalline BaM/$SiO_2$/Si(100) thin films were characterized by Rutherford backscattering (RBS), thermogravimetry (TGA), differential thermal analysis (DTA), x-ray diffraction (XRD), and vibrating sample magnetometry (VSM), as well as Fourier transform infrared spectroscopy (FTIR). The perpendicular coercivity $H_{C\bot}$ and in-plane coercivity $H_{CII}$ after annealing at 650${\circ}C$ for 2 hours were 4766 Oe and 4480 Oe, respectively, at room temperature, under a maximum applied field of 10 kOe.

• 한국응용과학기술학회지
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• 제16권3호
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• pp.255-262
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• 1999

The new copolymers which contain flexible spacers in main chain were prepared and their properties were studied. the copolymers were synthesized in the melt polymerization melted from diacetoxynaphthalene isomers, ${\alpha},{\omega}bis(4-carboxyphenoxy)$ alkanes and p-acetoxy benzoic acid in the molar ratio of 1:1:2 and characterized for the effects of structure of naphthalenediol isomer moieties and the spacers on thermal crystalline and liquid crystalline properties of the resulting polymers. Diacetoxy naphthalene isomers were used 1. 5-,1. 6-,2. 6-and 2. 7-disubstituted ones and the spacers was either tetramethylene or decamethylene. The polymer was characterized by elemental and spectropic analysis, differential scanning calorimetry (DSC) on a polaring microscope, wide-angle X-ray diffractometry and thermogravimetry (TGA). There glass transition temperatures (Tg) and melting temperature (Tm) on the structure of the naphthalenediol isomer moieties and the length of the spacers. The presence of spacers was found to the helpful in crystallization of 1. 6-naphthalenediol copolyesters. The presence of amide group in the backbone chain of polymer was found to increase transition temperature, crystallization, thermal stability of polymers but to decreas solubility.

• 대한화학회지
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• 제27권3호
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• pp.224-232
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• 1983

$Fe_2O_3$와 $BaCO_3$ 분체를 철제 ball-mill로 각각 5, 15, 30, 80, 200시간 혼합분쇄하여 얻어진 $BaCO_3-Fe_2O_3$계에서 고체반응 및 생성 Ba-ferrite의 자기적 성질에 미치는 분쇄시간의 영향을 조사하였다. 열천칭, X-선 회절기, 주사형전자현미경 및 B-H 이력곡선기 등을 사용하여 조사한 결과 일정시간 이상 분쇄시켰을 때 입자의 응집현상과 함께 초상자성을 띄는 미립자가 생기게 되어 Ba-ferrite의 생성 및 자기적 성질에 중요한 영향을 미친다는 사실을 확인했다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.471.1-471.1
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• 2014

염료감응형 태양전지(DSSC)는 다양한 태양전지 중, 가장 환경친화적이고, 생산단가도 낮을 뿐만 아니라 다양한 색상과 투광성을 확보할 수 있어 많은 연구가 진행되어왔다. 하지만 액체전해질을 사용하는 기존 염료감응형 태양전지는 높은 휘발성과 열 팽창 수축에 따른 전해질 누액의 문제점으로 인하여 최근에는 고체전해질을 이용한 염료감응형 태양전지의 개발이 활발히 이루어지고 있다. 또한 기존 염료보다 높은 흡광계수와 넓은 흡수스펙트럼을 지닌 페로브스카이트가 개발되어 현재 많은 관심이 주목되고 있다. 본 연구에서는 $TiO_2$ 제조상의 중간생성물인 Metatitanic acid (MTA)를 이용하여 광전극을 형성하고 열처리 온도에 따른 나노입자의 소성거동평가을 평가하였고 시차열중량 분석, 결정상 확인을 하고 염료감응 태양전지에 적용하였다. MTA 나노입자를 Field Emission Transmission Electron Microscopy (FE-TEM), Barrett-Joyner-Halenda (BJH pore size distribution)과 Brunauer-Emmet-Teller (BET) 분석을 통해 소성거동을 평가하고, Thermogravimetry and differential thermal analysis (TG-DTA)를 통해 열중량 측정을 하였으며, X-ray Diffraction (XRD) 분석을 통해 결정상을 확인하였다. 또한 Fourier-transform infrared (FT-IR) spectroscopy를 통해 MTA 나노입자의 표면분석을 하였다. 형성된 MTA 광전극을 페로브스카이트 염료에 적용하여 5%의 효율을 달성하였다.

• 대한의용생체공학회:의공학회지
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• 제8권1호
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• pp.29-40
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• 1987

2-Hydroxyethyl methacrylate(HEMA) was copolymerized with allyltrimethylsilane- (ATMS) and allylt.imethoxysilane(ATMOS) at 70。C in N, N'dimethylformamide- (DMV) using $\alpha$ , $\alpha$'-azobisisobutyronitrile(AIBN). The compositions of unreacted monomers were determined by gas chromatographic analysis. The monomer reactivity ratios were determined by Fireman-Ross, Helen-Tiidus and intersection methods. The average values are as follows : $$r_1(HEMA) : 6.62 $\pm$ 0.07, r_2(ATMS) : 0.07 $\pm$ 0.01 for HEMA-ATMS system.$$ $$r_l(HEMA) : 4.09 $\pm$ 0.14, r_2(ATMOS) : 0.06 $\pm$ 0.01 for HEMA-ATMOS toys tem.$$ The lower rl(HEMA) In the HEMA-ATMOS system as compared to HEMA ATMS system may be contributed to higher relative reactivity of ATMOS toward the poly(HEMA) radical. The compositions of synthesized copolymers were determined from silicon con tents estimated gravimetrically. The thermal stabilities of the copolymers were investigated by thermogravimetry(TG). The enthalpic changes associated with the endothermic transition were evaluated by differential scanning calorimetry(DSC). The swelling properties of the copolymers in water were also investigated.

• Journal of the Korean Wood Science and Technology
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• 제42권6호
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• pp.675-681
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• 2014

최근 친환경 재료에 대한 국민들의 관심이 높아지면서 실내사용목재의 이용도 증가하고 있다. 본 연구는 실내사용 목재의 내화성 부여를 위한 기초자료로 활용될 수 있는 열특성 분석에 그 목적이 있다. 열방출률과 열방출량, 가스발생량, 중량감소 등의 연소성질을 열중량 분석(TGA) 및 콘칼로리미터(KS F ISO 5660-1)의 방법으로 분석하였다. 분석결과 목재의 재질적 특성은 연소적 특성으로 발현되었으며, 열적성질과 연소가스 발생량과의 관계는 상관관계가 높게 나타났다. 탄화층 형성에 의한 연소억제 효과도 수종에 따라 현저한 차이를 보였다. 총열방출량과 중량감소량은 상관관계가 높게 나타났다. 점화시간과 총열방출량 등의 자료는 목재의 내화성능부여 등의 기초 자료로서 매우 중요하리라 판단되었다.

• Elastomers and Composites
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• 제23권4호
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• pp.289-298
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• 1988

The thermal degradation of poly(methyl methacrylate)(PMMA) and poly($\alpha$-methylstyrene-co-acrylonitrile)(SAN) mixtures were carried out using the thermogravimetry(TG) and differential scanning calorimetry(DSC) in the stream of nitrogen and air with 50 ml/min at the various heating rate from 4 to $20^{\circ}C/min$ and temperature from 20 to $500^{\circ}C$. The value of activation energies of thermal degradation determined by TG and DSC in the various PMMA/SAN mixtures were 34-54 kcal/mol in the stream of nitrogen. The value of activation energy of SAN 60% mixture were appeared high in comparison with addition rule. PMMA/SAN mixtures by the analysis of infrared spectrophotometer were decomposed by main chain scission in the stream of nitrogen.

• Elastomers and Composites
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• 제24권1호
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• pp.11-18
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• 1989

The thermal degradation of Poly(methyl methacrylate) (PMMA) and poly(acrylonitrile butadiene styrene)(ABS) terpolymer as well as their mixtures were carried out using the thermogravimetry and differential scanning calorimetry(DSC) in the stream of nitrogen and air with 50 ml/min at the various heating rate from 4 to $20^{\circ}C/min$ and temperature from 200 to $300^{\circ}C$ The values of activation energies of thermal degradation determined by TG and DSC in the various PMMA/ABS mixtures were $34{\sim}58Kcal/mol,\;35{\sim}54Kcal/mol$ in the stream of nitrogen. The values of activation energy of ABS20% mixture was appeared high in camparison with addition rule. According to increasing the composition of ABS, the temperatures of glass transition and initial decomposition temperature were increased. PMMA/ABS mixtures by the analysis of infrared spectrophotometer were decomposed by main chain scission in the stream of nitrogen.

• 대한금속재료학회지
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• 제48권4호
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• pp.315-319
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• 2010

In this study, the hydrogen reduction behavior of ball-milled NiO nanopowder was investigated depending on the partial pressure of water vapor. The hydrogen reduction behavior was analyzed by thermogravimetry and hygrometry under heating to 873 K in hydrogen. In order to change the partial pressure of the water vapor, the dew point of hydrogen was controlled in the range of 248 K~293 K by passing high-purity hydrogen through a saturator that contained water. Interestingly, with the increase in the dew point of the hydrogen atmosphere, the first step of the hydrogen reduction process decreased and the second step gradually increased. After the first step, a pore volume analysis revealed that the pore size distribution in the condition with a higher water vapor pressure shifted to a larger size, whereas the opposite appearedat a lower pressure. Thus, it was found that the decrease in the pore volume during the chemical reaction controlled process at a dew point of 248 K caused a reduction in retardation in the diffusion controlled process.

• 한국재료학회지
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• 제22권4호
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• pp.207-210
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• 2012

The preparation of $Sm_2O_3$ doped $CeO_2$ in Igepal CO-520/cyclohexane reverse micelle solutions has been studied. In the present work, we synthesized nanosized $Sm_2O_3$ doped $CeO_2$ powders by reverse micelle process using aqueous ammonia as the precipitant; hydroxide precursor was obtained from nitrate solutions dispersed in the nanosized aqueous domains of a micro emulsion consisting of cyclohexane as the oil phase, and poly (xoyethylene) nonylphenylether (Igepal CO-520) as the non-ionic surfactant. The synthesized and calcined powders were characterized by Thermogravimetry-differential thermal analysis (TGA-DTA), X-ray diffraction analysis (XRD), and Transmission electron microscopy (TEM). The crystallite size was found to increase with increase in water to surfactant (R) molar ratio. Average particle size and distribution of the synthesized $Sm_2O_3$ doped $CeO_2$ were below 10 nm and narrow, respectively. TG-DTA analysis shows that phase of $Sm_2O_3$ doped $CeO_2$ nanoparticles changed from monoclinic to tetragonal at approximately $560^{\circ}C$. The phase of the synthesized $Sm_2O_3$ doped $CeO_2$ with heating to $600^{\circ}C$ for 30 min was tetragonal $CeO_2$. This study revealed that the particle formation process in reverse micelles is based on a two step model. The rapid first step is the complete reduction of the metal to the zero valence state. The second step is growth, via reagent exchanges between micelles through the inter-micellar exchange.