• 한국응용과학기술학회지
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• 제17권2호
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• pp.132-138
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• 2000

Excess enthalpies ($H^{E}$) were measured by isothermal flow calorimetry for the nonionic amphiphile 2-butoxyethanol/water mixtures at 10 different temperatures (48.5 to $70^{\circ}C$) around and above the lower consolute solution temperature, $T_{lc}$. $H^{E}$ exhibits U-shape for the binary mixtures, and is large and negative which reflects substantial interaction between two chemical species. When the commonly used, semi-empirical Redlich-Kister (RK) polynomials were fitted to the measured $H^{E}$, plots of $H^{E}$ vs. weight fraction provided more accurate fitting with fewer parameters than conventionally drawn $H^{E}$ vs. mole fraction plots. This was due to the enhanced symmetry of $H^{E}$ vs. weight fraction plots. Using the fitted Redlich-Kister polynomials and the Gibbs-Helmholtz relation, temperature dependence of the activity coefficients were found and compared to the values determined from vapor-liquid equilibria. The activity coefficients were in the range of one to three, indicating that the binary system deviates from ideality but not substantially. They slightly depended on temperature and the temperature effect was equivalent to 10 % change in the activity coefficients.

• 수산해양교육연구
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• 제14권2호
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• pp.177-190
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• 2002

An experimental study was carried out to make clear heat transfer characteristics in flow boiling of binary mixtures of refrigerants R134a and R123 in a uniformly heated horizontal tube. Experiments were run at a pressure of 0.6 MPa both for pure fluids and mixtures in the ranges of heat flux $10{\sim}50{kW/m}^2$, vapor quality 0~100% and mass flux 150-600 $kg/m^2s$. Heat transfer coefficients of mixtures were reduced compared to the interpolated values between pure fluids both in the low quality region where the nucleate boiling is dominant and in the high quality region where the convective evaporation is dominant. Total pressure drop during two-phase flow boiling in a horizontal tube consists of the sum of two components, that is, the frictional pressure drop and pressure drop due to acceleration. The frictional pressure drop is the most difficult component to predict, and makes the most important contribution to the total pressure drop. On the other hand, the acceleration pressure drop resulting from the variation of the momentum flux caused by phase change is generally small as compared to the frictional pressure drop. There is no significant difference in measured pressure drop between mixtures and pure fluids. The correlation of Martinelli and Nelson predicted most of the present data both for pure and mixed refrigerants within 30%.

• 대한화학회지
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• 제29권5호
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• pp.465-471
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• 1985

메탄올-아세토니트릴, 메탄올-아세톤, 에탄올-아세토니트릴 및 에탄올-아세톤의 이성분 혼합용매에서 2-염화 안트라퀴논 카르보닐의 가용매분해반응 속도상수를 전기전도도법으로 측정하였다. 메탄올-아세토니트릴 이성분 혼합용매계에서는 메탄올의 몰분율 $X_{MeOH}$ = 0.73∼0.81에서, 메탄올-아세톤 이성분 혼합용매계에서는 메탄올의 몰분율 $X_{MeOH}$ = 0.83에서 각각 최대 반응속도 현상이 나타났다. Kivinen 관계식과 Grunwald-Winstein 관계식등의 적용으로 부터 본 반응이 $S_N2$형태의 반응메카니즘으로 진행함을 알 수 있었다. Taft의 분광용매화 관계식의 적용으로 부터 메탄올-아세토니트릴 및 메탄올-아세톤 혼합용매계에서는 용매의 수소결합주게효과(${\alpha}$)와 극성-편극성 효과가 중요하게 작용함을 알 수 있었으며, 에탄올의 이성분 혼합용매계에서는 용매의 수소결합주게 효과만 이 반응에 크게 기여함을 알 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제12권6호
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• pp.909-915
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• 2002

The biodegradation of BTEX components (benzene, toluene, ethylbenzene, o-xylene, m-xylene, and p-xylene) individually and in mixtures was investigated using the o-xylene-degrading thermo-tolerant bacterium Ralsronia sp. strain PHS1 , which utilizes benzene, toluene, ethylbenzene, or o-xylene as its sole carbon source. The results showed that as a single substrate for growth, benzene was superior to both toluene and ethylbenzene. While growth inhibition was severe at higher o-xylene concentrations, no inhibition was observed (up to 100 mg $l^-1$) with ethylbenzene. In mixtures of BTEX compounds, the PHS1 culture was shown to degrade all six BTEX components and the degradation rates were in the order of benzene, toluene, o-xylene, ethylbenzene, and m- and p-xylene. m-Xylene and p-xylene were found to be co-metabolized by this microorganism in the presence of the growth-supporting BTEX compounds. In binary mixtures containing the growth substrates (benzene, toluene, ethylbenzene. and o-xylene), PHS1 degraded each BTEX compound faster when it was alone than when it was a component of a BTEX mixture, although the degree of inhibition varied according to the substrates in the mixtures. p-Xylene was shown to be the most potent inhibitor of BTEX biodegradation in binary mixtures. On the other hand, the degradation rates of the non-growth substrates (m-xylene and p-xylene) were significantly enhanced by the addition of growth substrates. The substrate utilization patterns between PHS1 and other microorganisms were also examined.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2004년도 International Symposium on Powder Materials and Processing
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• pp.114-114
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• 2004

• 한국고분자학회지:고분자과학과기술
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• 제5권4호
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• pp.328-335
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• 1994

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2003년도 춘계학술강연 및 발표대회
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• pp.22-22
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• 2003

• 에너지공학
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• 제24권4호
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• pp.18-23
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• 2015

인화점은 인화성에 따라 가연성 액체들을 분류하기 위해 사용된다. 인화점은 인화성 액체를 안전하게 저장, 취급 수송하기 위한 중요한 정보이다. Tag 개방식 장치를 이용하여 두 개의 이성분계 혼합물($CCl_4+o-xylene$ and $CCl_4+p-xylene$)의 인화점을 측정하였다. 또한 라울의 법칙, UNIQUAC 식, 경험식을 이용하여 인화점을 계산하여 그 값을 측정치와 비교하였다. 이 중 경험식에 의한 인화점 계산치가 가장 측정치를 잘 모사하였다.

• International Journal of Air-Conditioning and Refrigeration
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• 제9권3호
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• pp.1-9
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• 2001

In this study, condensation heat transfer coefficients (HTCs) of nonazeotropic refrigerant mixtures of HFC32/HFC 134a and HCFC123 at various compositions were measured on a horizontal smooth tube. All data were taken at the vapor temperature of 39$^{\circ}C$ with a wall subcooling of 3~8K. Test results showed that HTCs of tested mixtures were 11.0~85.0% lowed than the ideal values calculated by the mass fraction weighting of the HTCs of the pure components. Thermal resistance due to the diffusion vapor film was partly responsible for the significant reduction of HTCs with these nonazeotropic mixtures. The measured data were compared against thc predicted ones by Colburn and Drew's film model and a good agreement was observed within a deviation of 15%.

• Bulletin of the Korean Chemical Society
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• 제25권9호
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• pp.1403-1407
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• 2004

Dielectric relaxation measurements on 3-nitrotoluene (3-NT) mixture of dimethylacetamide (DMA), dimethylformamide (DMF) and dimethysulphoxide (DMSO) have been carried out across the entire concentration range using Time domain reflectometry technique at 15, 25, 35 and $45^{\circ}C$ over the frequency range from 10 MHz to 20 GHz. For all the mixtures, only one dielectric loss peak was observed in this frequency range and the relaxation in these mixtures can be well described by a single relaxation time using Debye model. Bilinear calibration method is used to obtain complex permittivity ${\varepsilon}^{*}({\omega})$ from complex reflection coefficient ${\rho}^{*}({\omega})$ over frequency range 10 MHz to 20 GHz. The excess permittivity, excess inverse relaxation time, Kirkwood correlation factor, molar energy of activation are also calculated for these mixtures to study the solute-solvent interaction.