• Bulletin of the Korean Chemical Society
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• 제6권1호
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• pp.33-36
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• 1985

The luminescence intensity of $Tb^{3+}$ bound to picolinic acid, squaric acid, and 2,3-pyrazinedicarboxylic acid has been studied in water and water-ethanol mixtures. It has been found that the emission intensity of $Tb^{3+}$ in the complexes is enhanced with the increase of ethanol content in water-ethanol mixtures. Several factors affecting on the emission intensity of $Tb^{3+}$ in waterethanol mixtures are discussed.

• Korean Chemical Engineering Research
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• 제43권2호
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• pp.243-248
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• 2005

분리막 투과증발은 증류에 비하여 낮은 에너지를 요구하기 때문에 물/유기물 혼합물의 분리에 이용될 수 있으며 공비 혼합물이나 이성질체의 분리에 선호되는 방법이다. 제올라이트 분리막은 고분자 분리막에 비하여 열적, 기계적, 화학적 안정성이 우수하며 NaA 제올라이트 분리막은 큰 친수성을 나타내므로 물/유기물 혼합물로부터 효율적인 물 분리에 적합하다. 본 연구에서는 NaA 제올라이트 분리막을 이용한 투과증발 막분리 공정을 이용하여 물/에탄올 혼합물에서 선택적으로 물을 분리하고자 하였다. 에탄올의 공급 농도가 증가함에 따라 총투과플럭스는 감소하였으며 선택도는 증가한 후 높은 에탄올 농도에서 감소하는 것을 관찰할 수 있었다. 실험 온도의 증가에 따라 총투과플럭스는 증가하였으며 선택도 또한 증가하였지만 높은 에탄올 농도에서는 감소하였다. 160시간 이상의 장기간 실험을 통하여 총투과플럭스와 선택도가 안정적으로 일정함을 확인할 수 있었다. 또한, 본 연구를 통하여 얻어진 NaA 제올라이트 분리막은 증류 및 PVA 계열 고분자 분리막보다 우수한 성능을 나타냄을 알 수 있었다.

• 한국농공학회지
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• 제39권2호
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• pp.26-31
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• 1997

Abstract A series of permeability tests was performed on the mixtures with specific mixing rates of sand and bentonite using modified rigid-wall permeameter. Sand-bentonite mixtures were permeated by organics, ethanol and TCE. Permeability of bentonite with several mixing rates had a tendency to decrease up to initial one pore volume and permeability was thereafter converged to a constant value. When sand-bentonite mixtures was permeated by water, permeability was decreased at the beginning but it was thereafter converged to a constant. Among several mixing rates, permeability was greatly decreased at 15% of mixing rate. When sand-bentonite mixtures with 15% mixing rate was permeated by ethanol, permeability was about 10 times larger value than permeability of water. Peameability was shown greater values when permeated by TCE (TrichloroEthylene) followed by ethanol. Suitable mixing rate of sand-bentonite for a liner of waste landfills was detected.

• 한국농공학회지
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• 제39권2호
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• pp.32-43
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• 1997

Abstract A series of permeability tests was performed on the mixtures with specific mixing rates of sand and bentonite using modified rigid-wall permeameter. Sand-bentonite mixtures were permeated by organics, ethanol and TCE. Permeability of bentonite with several mixing rates had a tendency to decrease up to initial one pore volume and permeability was thereafter converged to a constant value. When sand-bentonite mixtures was permeated by water, permeability was decreased at the beginning but it was thereafter converged to a constant. Among several mixing rates, permeability was greatly decreased at 15% of mixing rate. When sand-bentonite mixtures with 15% mixing rate was permeated by ethanol, permeability was about 10 times larger value than permeability of water. Peameability was shown greater values when permeated by TCE (TrichloroEthylene) followed by ethanol. Suitable mixing rate of sand-bentonite for a liner of waste landfills was detected.

• 한국화재소방학회논문지
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• 제29권2호
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• pp.39-43
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• 2015

인화점은 액체 혼합물의 화재와 폭발의 위험성을 특징짓는 주된 성질이다. 인화점은 가연성 액체에 불꽃이 가해졌을 때 점화가 발생하는 가장 낮은 온도로 정의된다. Seta flash 밀폐식 장치를 이용하여 이성분계 수용성 혼합물인 water-methanol계와 water-ethanol계의 인화점을 측정하였다. Wilson 식과 UNIQUAC 식과 같은 활동도 모델식을 활용한 방법을 이용하여 인화점을 계산하였다. 이 계산치와 라울의 법칙에 의한 계산치를 비교하였다. 그 결과, 활동도 계수 모델식에 의한 계산치가 라울의 법칙에 의한 계산치 보다 측정값에 보다 근접하였다.

• Bulletin of the Korean Chemical Society
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• 제18권9호
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• pp.1017-1021
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• 1997

Solvolyses of p-methoxyphenyl chloroformate in water, D2O, CH3OD, 50% D2O-CH3OD, and in aqueous binary mixtures of acetone, ethanol and methanol are investigated at 25.0 ℃. Product selectivities are reported at 25 ℃ for a wide range of ethanol-water and methanol-water solvent compositions. The Grunwald-Winstein plots of first-order rate constants for p-methoxyphenyl chloroformate with YCl (based on 1-adamantyl chloride) show marked dispersions into three separate curves for the three aqueous mixtures with a small m value and a rate maximum for aqueous alcohol solvents. Third-order rate constants, kww, kaw, kwa and kaa were calculated from the observed kww and kaa values together with kaw and kwa calculated from the intercept and slope of the plot of 1/S vs. [alcohol]/[water]. The calculated rate constants, kcalc and mol % of ester agree satisfactorily with those of the observed rate constants, kobs and mol % of ester, supporting the stoichiometric solvation effect analysis. The kinetic solvent isotope effects determined in water and methanol are consistent with the proposed mechanism of the general base catalyzed carbonyl addition-elimination.

• Bulletin of the Korean Chemical Society
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• 제24권9호
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• pp.1293-1302
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• 2003

Rate constants at various temperatures and activation parameters are reported for solvolyses of acyl chlorides (RCOCl), with R = Me, Et, i-Pr, t-Bu, cyclopentylmethyl, benzyl, thiophenylmethyl, 2-phenylethyl, diphenylmethyl, and phenylthiomethyl in 100% ethanol, 100% 2,2,2-trifluoroethanol (TFE), 80% v/v ethanol/ water and 97% w/w TFE/water. Additional rate constants for solvolyses with R = Me, t-Bu, and $PhCH_2$ are reported for TFE/water and TFE/ethanol mixtures, and for solvolyses with R = t-Bu, and PhCH2 are reported for 1,1,1,3,3,3-hexafluoropropan-2-ol/water mixtures, as well as selected kinetic solvent isotope effects (MeOH/MeOD and TFE). Taft plots show that electron withdrawing groups (EWG) decrease reactivity significantly in TFE, but increase reactivity slightly in ethanol. Correlation of solvent effects using the extended Grunwald-Winstein (GW) equation shows an increasing sensitivity to solvent nucleophilicity for EWG. The effect of solvent stoichiometry in assumed third order reactions is evaluated for TFE/ethanol mixtures, which do not fit well in GW plots for R = Me, and t-Bu, and it is proposed that one molecule of TFE may have a specific role as electrophile; in contrast, reactions of substrates containing an EWG can be explained by third order reactions in which one molecule of solvent (ethanol or TFE) acts as a nucleophile, and a molecule of ethanol acts as a general base catalyst. Isokinetic relationships are also investigated.

• Bulletin of the Korean Chemical Society
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• 제6권5호
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• pp.259-263
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• 1985

Rate Constants for the solvolysis of p-methylbenzyl chloride in various ethanol-water mixtures were studied at 30 and $40^{\circ}C$ under various pressures up to 1600 bar. The rates of reaction were increased with increasing temperature and pressure, and decreased with increasing solvent composition of ethanol mole fraction. From the rate constants, the values of the activation parameters (${\Delta}V^{\neq},{\Delta}{\beta}^{\neq},{\Delta}H^{\neq}\;and\;{\Delta}S^{\neq}$) were evaluated. The values of ${\Delta}V^{\neq}\;and\;{\Delta}{\beta}^{\neq}$ exhibit the extremum behavior at about 0.30 mole fraction of ethanol. This behavior is discussed in terms of solvent structure variation (electrostriction). From the relation between the reaction rate and the dielectric constant of solvent or the number of water molecule participated in the transition state, it could be postulated that the reaction proceeds through $S_N1$ mechanism.

• 공업화학
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• 제7권6호
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• pp.1087-1095
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• 1996

Poly(dimethyl siloxane)막을 이용하여 $45^{\circ}C$에서 에탄올/이소프로판올/물의 삼성분 혼합물에 대한 투과증발실험을 행하고, 에탄올과 이소프로판올의 존재가 상호의 투과특성에 미치는 영향을 연구하였다. 에탄올과 이소프로판올은 각각 상호의 투과속도를 감소시키는 경향을 나타내었으며, 이소프로판올이 에탄올의 투과에 미치는 영향보다는 에탄올이 이소프로판올의 투과에 미치는 영향이 더 현저하였다. 투과속도의 감소는 고분자막에 대한 에탄올이나 이소프로판올의 가소화 영향보다는 투과성분 사이의 상호작용에 의한 영향이 더 크기 때문으로 생각되었다. 삼성분 혼합물에서 투과성분 사이의 강한 상호작용은 에탄올과 이소프로판올의 투과에 대한 추진력을 감소시키는 결과를 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2377-2381
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• 2007

Solvolyses of 3,4-dimethoxybenzenesulfonyl chloride (DSC) in water, D2O, CH3OD, and in aqueous binary mixtures of acetone, acetonitrile, 1,4-dioxane, ethanol, methanol, and 2,2,2-trifluoroethanol (TFE) have been investigated at 25.0 oC. Kinetic solvent isotope effects (KSIE) in water and in methanol and product selectivities in alcohol-water mixtures are also reported. The Grunwald-Winstein plot of first-order rate constants for the solvolyic reaction of DSC with YCl shows marked dispersions into separated lines for various aqueous mixtures. With use of the extended Grunwald-Winstein equation, the l and m values obtained are 1.12 and 0.58 respectively for the solvolyses of DSC. The relatively large magnitude of l is consistent with substantial nucleophilic solvent assistance. From Grunwald-Winstein plots the rate data are dissected approximately into contributions from two competing reaction channels. This interpretation is supported for alcohol-water mixtures by the trends of product selectivities, which show a maximum for ethanol-water mixtures. From the KSIE of 1.45 in methanol, it is proposed that the reaction channel favored in methanolwater mixtures and in all less polar media is general-base catalysed and/or is possibly (but less likely) an addition-elimination pathway. Also, the KISE value of 1.35 for DSC in water is expected for SN2-SN1 processes, with minimal general base catalysis, and this mechanism is proposed for solvolyses in the most polar media.