• Journal of the Korean Chemical Society
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• v.36 no.6
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• pp.796-801
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• 1992

An empirical Lewis basicity, DN, for eight mixed methanol solvents has been measured by the solvatochromic behavior of the [Cu(tmen)(acac)]$CIO_4$. The change of DN in mixed methanol solvents is not correlated with composition of the mixtures and divided into three groups: (1) dipolar aprotic solvents contribute mainly to the solvation of solute (MeOH-DMSO, MeOH-PY, MeOH-DMF), (2) two components of mixture contribute equally to the solvation of solute (MeOH-MeCN, MeOH-dioxane, MeOH-AC) and (3) methanol contributes entirely to the solvation of solute (MeOH-DCE, MeOH-TCE). The relationship between DN and Kamlet-Taft's $B_{KT}$ for mixed methanol solvents was found to agree well. These DN values also were a useful factor to analysis of reactivity for mixed methanol solvents.

• The Korean Journal of Rheology
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• v.6 no.1
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• pp.20-29
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• 1994

본 논문에서는 실리콘 오일을 용매로 사용하여 조성된 전기유동유체의 전기장 부하 변화에 따른 역학적 특성을 고찰하였으며 그응용성에 대하여 연구하였다. 유체에 가해지는 전기장은 0~0.25kV/mm까지 변화시켰고 외부에서 가해지는 회전력은 0∼500rpm까지의 범위로 설정하였으며 용매의 점성계수 및 각각의 용매에 대한 입자 중량비를 달리하여 자체 조성한 4종류의 전기유동유체에 대하여 특성을 고찰하였고, 전기유동유체의 항복응력도 부 하되는 전기장의 함수로 증가함을 알수 있었다. 또한 부하되는 전기장의 크기 뿐만이 아니 라 입자의 중량비 용매의 점성계수도 전기유동유체의 거동에 많은 영향을 미침을 알수 있었 다. 또한, 전기유동유체를 이용한 응용예로서 지능구조물을 제작하여 전기장에 따른 진동특 성변화를 고찰하였다. 실험결과 부하되는 전기장의 강도가 증가함에 따라 구조물의 고유진 동수가 점차적으로 증가하였으며 입자의 중량비가 증가할수록 증가폭이 커 넓은 범위의 제 어영역을 가짐을 알수 있었다. 전기유동유체의 진동제어 이용가능성을 입증하기 위하여 시 간영역에서 구조물의 전기장에 대한 과도 진동제어 응답과 강제진동제어 응답을 실험하였다.

• KSBB Journal
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• v.16 no.1
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• pp.95-98
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• 2001

Various factors affecting the supercritical carbon dioxide extraction of daidzein from soybean were studied. Daidzein was not extracted with pure supercritical carbon dioxide. The ethanol was an efficient modifier for supercritical carbon dioxide to extract daidzein. The extraction efficiency increased as the pressure increased up to 300 bar. At $35^{\circ}C$ and 300 bar, 93% of daidzein was extracted with supercritical carbon dioxide modified with 15% of ethanol.

• Journal of the Korean Chemical Society
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• v.24 no.6
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• pp.444-451
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• 1980

In order to further elucidate the process of electron solvation in liquids, the medium effect, as the difference between the free energy of $H^+$ in aqueous and non-aqueous states (${\Delta}{\Delta}G_0$), of THF-water mixtures has been investigated. (${\Delta}{\Delta}G_0$) were determined by electromotive force masurements of the cell Pt$H_2Q$, Q, HCI, THF, $H_2O$|KC1 | $Hg_2Cl_2$|Hg(Pt), where $H_2Q$ and Q are hydroquinone and quinone respectively. The effect of dielectric constant on the difference of free energy and the absorption energy of solvated electrons have been studied. For the consideration of these effect the polymerization of water in THF has been studied. Near infrared spectrum of O-H stetching energy has been used to measure the extent of water aggregates. The expermental results indicate that at least in some composition of binary mixtures the electrons or other ions are solvated preferentially with one component of solvents.

• Analytical Science and Technology
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• v.22 no.2
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• pp.159-165
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• 2009

The thermochromism of fluoran has been examined. The DCF exists as a colorless lactone in aprotic solvents. However, the DCF exists in the form of an equilibrium mixture of a colored zwitter-ion and a colorless lactone in protic solvents. When an acid is added to the solution, the DCF exists an equilibrium mixture as a colorless lactone and a colored cation even in aprotic solvents. In order to understand the interaction between the DCF and the solvent, absorption spectra of the DCF in various solvents were measured. The thermodynamic parameters of the DCF have also been investigated. From the variation of absorbance with temperature, the standard enthalpy changes ${\Delta}H^0$ of the equilibrium between the lactone and the zwitter-ion in various solvents have been determined. The standard enthalpy change ${\Delta}H^0$ is approximately -2.0 kJ/mol in protic solvents. In acidic solution, the standard enthalpy change is measured to be to zero in protic solvents within the experimental error. When the carboxylic group is protonated in acidic solution, a poor interaction between the dye and the solvent is expected.

• Polymer(Korea)
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• v.24 no.1
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• pp.23-28
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• 2000

Autoadhesion strength of PS/PS Interfaces in solvent welding was determined as a function of processing conditions by butt joint test. It was verified that the chain mobility and surface roughness at PS/PS interface were enhanced by the applied solvent having a similar solubility parameter as PS and resulted in the dramatic improvement of autoadhesion strength at PS/PS interface. It was found that the mechanism of solvent welding is dependent upon the chain mobility due to the diffusion of solvent to PS interface and the contact area at interface. When the welding temperature is lower than the boiling point of applied solvent, the effect of chain mobility on autoadhesion strength was dominated, while contact area took more important role when welding temperature is above the boiling point of solvent. Autoadhesion strength increased with increasing contact time and contact temperature but :he effect of solvent on autoadhesion strength became smaller.

• Korean Chemical Engineering Research
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• v.58 no.1
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• pp.92-97
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• 2020

In this study, the solubilities of a pharmaceutical compound, nifedipine, in three mixed solvents were determined. In addition, the nifedipine, that was dissolved in solvents (acetone, DMF, methylene chloride), was recrystallized using antisolvents (water, hexane, carbon dioxide) The external shape, size, and melting point of the crystallized nifedipine were measured. As the mixed solvents, acetone+water, DMF+water, and methylene chloride+hexane were used, and the solubility of nifedipine decreased with increasing antisolvent concentrations in the mixtures. In case of acetone+water, the solubility maximum was observed due to the density anomaly of the mixture, and this phenomenon was not observed in other systems. The crystallized nifedipine particles exhibited the bladed, equant, and prismatic habits, and the particles size was significantly reduced compared to the raw material. The average particle size of raw nifedipine was 337 ㎛, and the size of crystallized particles was in the range of 11.6~69.8 ㎛. All the crystallized nifedipine particles had the same thermal behavior and this result was not influenced by the change of solvent and antisolvent.

• Proceedings of the Membrane Society of Korea Conference
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• 1996.10a
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• pp.53-54
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• 1996

비대칭 분리막의 제조에 있어서는 용매와 비용매의 교환에 의한 상분리 현상을 이용하기 때문에 용매와 비용매의 성질이 막 제조 공정에 중요한 변수가 된다. 고분자 용액에 공용매를 첨가할 경우 용액의 점도, 용매와 비용매의 상호 작용 정도 등의 용액의 성질을 변화시킬 수 있다. 따라서 이들의 변화에 따른 분리막의 구조 변화를 관찰하여 그 상관 관계를 규명하면 분리막의 미세 구조 조절 및 제어가 가능할 것이다. 본 실험에서는 폴리이미드(PI)를 고분자로 사용하였고, 용매로는 NMP, 공용매로는 $\gamma$-butyrolactone($\gamma$-BL)을 사용하여 고분자의 농도가 15 wt%인 용액을 제조하였다. 제조한 용액을 유리판에 균일한 두께로 casting 한 후 물을 비용매로 사용하여 immersion precipitation 방법으로 막을 제조하였다. 제조한 막은 24시간 동안 물 속에 방치하여 용매를 충분히 제거한 후 상온에서 24시간 이상 건조시켰다. 투과도 측정은 soap bubble flow 방법으로 시행하였으며 단면 구조는 주사전자 현미경을 사용하여 관찰하였다.

• Journal of the Korean Chemical Society
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• v.28 no.4
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• pp.210-216
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• 1984

Solvatochromic comparison methods were applied to determine Taft's solvent parameters, ${\pi}^{\ast}$(solvent polarity-polarizability), ${\alpha}$(solvent hydrogen bond donor acidity) and ${\beta}$ (solvent hydrogen bond acceptor basicity) for MeOH-MeCN solvent mixtures. Swain's solvent parameters A(anion solvation scale) and B(cation solvation scale) were also determined by least square fitting of kinetic data in the same binary solvent mixtures. It was found that: (i)${\beta}$ depends on the basicity of the solvent and increases with the MeOH content owing to the increase in polymeric structure of methanol; (ii) ${\pi}^{\ast}$depends on the dipole moment of the solvent and increases with the MeCN content of the solvent; (iii) ${\alpha}$ increases rapidly with the MeOH content as the hydrogen bond donor acidity of the solvent mixtures increases. Taft's reaction constants a and s and Swain's reaction constants a and b were determined for the reactions reported from our laboratory previously using solvent parameters determined in this work. No meaningful inter-relationship was found between the two set of reaction parameters, but a good linear correlation was found between the ratios a/s and a/b. Solvent effect on the reaction mechanism, substituent effect and leaving group ability were examined in the light of these reaction constants ratios.

• Journal of the Korean Chemical Society
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• v.31 no.1
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• pp.25-30
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• 1987

Solvolysis of tert-butyl halides and 1-adamantyl tosylate in methanol-acetone mixtures and solvolysis of tert-butyl bromide in methanol-chloroform mixtures have been studied. Solvent ionizing power of methanol-acetone mixtures were calculated by the Grunwald-Winstein equation and discussed the Y value variation caused by substrate changes. Y values based on 1-adamantyl tosylate is superion to others since it varies in wide range for methanol-acetone mixtures. It was found that the order of electrophilic assistance to leaving group is OTs > Cl > Br > I.