• Journal of the Korean Electrochemical Society
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• v.1 no.1
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• pp.28-32
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• 1998

The electrochemical behavior of film and charge-discharge capacity of Li-ion cell in 1 M $LiPF_6/EC:DME$ (1 : 1, by volume ratio) electrolyte solution was studied using chronopotentiometry, cyclic voltammetry, chronoamperometry, and impedance spectroscopy. The first irreversible capacity was higher than the second irrversible capacity because of solvent decomposition. Especially, passivation film that is electron insulating and ionic conducting were formed on the MPCF by solvent decomposition during the first charge. The solvated Li is co-intercalated with solvent into MPCF electrode. Part of the MPCF is expoliated during co-intercalation of solvent-Li. The MPCF ends up nonuniformly covered by a relatively thick layer of exfoliated particles embedded in a matrix of product by solvent decomposition.

• Journal of the Korean Chemical Society
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• v.53 no.3
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• pp.325-334
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• 2009

Many bacteria that are capable to tolerate and degrade organic solvents have been isolated from seawater. However, their roles in the biodegradation of organic solvents in the marine environment have remained unknown. Aeromonas hydrophila IB$B_{ct4}$, isolated from Constanta seawater, was able to tolerate and degrade different organic solvents. Toluene, styrene, xylene isomers, ethylbenzene, with the logarithm of the partition coefficient in octanol-water mixture (log $P_{ow}$) between 2.64 and 3.17, were more toxic for bacterial cells, compared with propylbenzene, n-hexane, n-heptane, with log $P_{ow}$ between 3.69 and 4.39. There were revealed cellular and molecular modifications induced by organic solvents to Aeromonas hydrophila IB$B_{ct4}$. The study of cellular and molecular modifications induced by different organic solvents showed a complex response of bacterial cells to the presence of organic solvents in the culture media.

• Journal of the Korean Chemical Society
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• v.30 no.4
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• pp.352-358
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• 1986

An extensive experimental survey on the retention behaviors of phenols in the binary solvent system such as methanol-water, acetonitrile-water and tetrahydrofuran-water as well as the ternary solvent system such as methanol-acetonitrile-water and methanol-tetrahydrofuran-water is presented. A linear equation, which describes the capacity factor as a function of the solvent composition in the mobile phase and is able to predict the retention behaviors of phenols, was obtained. The iso-eluotropic lines for the binary and ternary solvent system are based on the equal strength of the methanol-water solvent which shows an optimum separation of the phenols used. The specific effect of each solute in the binary solvent system appeared to be larger than those in the ternary system.

• Journal of the Korean Chemical Society
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• v.28 no.6
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• pp.349-354
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• 1984

The relative viscosities and the osmotic coefficients of alkaline metal iodides (NaI, KI, RbI, CsI) in methanol, ethanol, dimethylsulfoxide (DMSO), and sulfolane (TMS) have been measured by Ubbelohde viscometer and vapor pressure osmometry at 45 ∼ $120^{\circ}C.$ The order of A and B coefficients in viscosity for alkaline metal iodides are MeOH > EtOH > TMS > DMSO, and TMS > EtOH > DMSO > MeOH. dB/dT values for the alkaline metal iodides are in the order of NaI > KI > RbI > CsI in the protic solvents, while those for the aprotic solvents are in the reverse order. The order of the osmotic coefficients for the alkaline metal iodides is EtOH > DMSO > MeOH > TMS.

• KSBB Journal
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• v.5 no.1
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• pp.9-17
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• 1990

The growth and fermentation profiles of Clostridium acetobutylicum KCTC 1037 were examined in batch and continuous modes with pH variation and phosphate limitation. Clostridium acetobutylicum KCTC 10 37 grew better at pH 4.5 than at pH 5.5 or 6.5. Acetate and butyrate were produced at pH 5.5, whereas culture at pH 4.5 produced acetone and butanol. Solvent production was increased by the phosphate limitation in a batch culture, but in a phosphate-limited continuous culture for 400 hours steady-state solventogenesis was not observed. The induction and maintenance of solventogenesis presumably require not only acidic condition or phosphate limitation but also favourable bioenergetic condition.

• Polymer(Korea)
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• v.32 no.5
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• pp.483-488
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• 2008

The effect of methylene chloride/1,3-dioxolane co-solvent on the crystallization in the optical polycarbonate film was investigated. Increasing 1,3-dioxolane content in co-solvent resulted in the crystallization due to the lowering of solvent evaporation rate during film drying process. The crystallization in PC film could be minimized by either controlling of solvent composition and increasing solvent drying temperature. It was found that the surface roughness of solution casting PC film was affected by both crystallization and solvent evaporation rate. This morphological effect by alternative solvent is ascribed to a large decrease in light transmissivity on the optical PC film.

• Proceedings of the KAIS Fall Conference
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• 2002.11a
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• pp.283-286
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• 2002

막-용매 추출을 이용하여 모사폐수로부터 페놀을 분리하였으며, 이때 미세기공 비친수성 중공사형 모듈을 사용하였다. 전체적인 시스템은 향류, 및 병류로 운영되었으며, 유기오염물은 tube 안쪽으로, 용매는 shell쪽으로 흐르게 하였다. MIBK를 추출용매로 사용하였으며, 페놀의 분리효율은 향류 흐름이 병류흐름보다 더 우수함을 알 수 있었다.

• Proceedings of the Membrane Society of Korea Conference
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• 1993.10a
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• pp.31-31
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• 1993

지금까지 내유기용매성 분리막의 소재로는 Polysulfone이 많이 사용되었으나 내유기용매성이 고도로 요구되는 분야에는 적합하지 않았다. 이의 해결을 위해서 Polyimide를 소재로한 분리막의 개발에 대한 연구가 많이 진행되고 있다. 그러나 Polyimide는 내열성, 내유기용매성 등이 우수한 반면 T$_g$가 높고 용해되지 않아서 가공하는데 많은 제약이 있는 단점을 가지고 있다. 또한 기존에 널리 사용되었던 2단계 합성방법, 즉 Polyimide 전구체인 Polyamic acid를 합성하고 이를 casting하여 film을 얻은 뒤 다시 고온으로 열처리하여 Polyimide를 제조하는 방법은 공정이 번거롭고 부분적으로 불용성을 나타내기도 하였다. 본 연구에서는 1단계 용액 증합법으로 용융성 Polyimide를 합성하여 이를 소재로 내유기용매성 분리막을 제조하였다. 1단계 중합벙는 Polyamic acid를 합성하고 이를 film으로 만드는 공정이 필요치 않으며, 공정이 비교적 간단하고 경제적으로 유리한 잇점이 있다.

• 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.22 no.1
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• pp.7-11
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• 1978

The reactions of 2,4-dinitroiodobenzene with para subtituted anilines in acetonitrile-methanol binary solvent mixtures have been studied. Rate constants for reactions in methanol rich solvents are greater than for reactions in acetonitrile rich solvents. Kinetic results show that the bond formation step is rate determining in the solvent system studied. The solvent effect can be explained by stabilization of the transition state by formation of hydrogen bond between oxygen atom of methanol and hydrogen atom of aniline.