• Korean Journal of Food Science and Technology
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• v.24 no.5
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• pp.504-510
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• 1992

Several single or mixed water-miscible organic solvent systems were investigated to develop the most effective solvent system for enzymatic synthesis of N-benzoylaspartame(BzAPM). The BzAPM was prepared by immobilized thermolysin with using N-benzoyl-L-aspartic acid(Bz-Asp) and L-phenylalanine methyl ester(PheOMe). The solubilities of BzAPM and L-phenylalanine were highest in 4.5% methanol(1.89 and 1.79%, respectively) among the solvents system investigated while a mixed solvent system of 25% dimethyl sulfoxide(DMSO) and 20% polyethylene glycol(PEG) 200 showed relatively high values. The synthetic activity of BzAPM as well as initial reaction rate were found to be high in 45% methanol, 45% DMSO and a mixed solvent of 25% DMSO and 20% PEM 200. The imobilized thermolysin was most stable in 25% DMSO and 20% PEG 200 during storage at $40^{\circ}C$ for 42 days. PheOMe in the same solvent system was also found fairly stable against non-enzymatic decomposition at $40^{\circ}C$. Based on the synthetic efficiency and stability, the solvent system containing 25% DMSO and 20% PEG 200 was selected to be appropriate for the enzymatic synthesis of BzAPM.

• Journal of Adhesion and Interface
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• v.2 no.4
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• pp.10-23
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• 2001

In order to increase the lower values of % grafting and monomer conversion in the emulsion graft polymerization of methylmethacrylate(MMA) onto sodium alginate (SA; a polymer electrolyte) with alginic acid-g-PMMA, the graft polymerization with water soluble (methanol and acetone) and insoluble solvents was carried out using a varity of solvent amounts and agitating rates. And some physical properties of the graft polymer were also investigated. In the polymerizations with water insoluble solvent, there were pronounced improvements in both % grafting and MMA conversion by the promotion of MMA diffusion from the core to the SA adsorpted on the outer layer of particle and that of MMA complex formation with SA. And the effect was larger for the solvents (cyclohexane, decalin) which do not dissolve PMMA. On the other hand, in the polymerization with water soluble solvent, there was an significant increase in MMA conversion and a considerable increase in the % grafting by the destruction of electrical double layer around the SA chains, abstracting the hydrated water in the layer and the effect was more potential in the case of methanol which is a precipitant of PMMA.

• Proceedings of the Korea Association of Crystal Growth Conference
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• 1997.10a
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• pp.105-109
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• 1997

요소결정성장에 용매와 불순물이 주는 영향을 Monte Carlo법과 분자동역학법을 통해 분석하였으며 이를 통해 불순물인 Biuret이 결정의 Morphology에 대한 영향뿐만 아니라 내부격자에 용매인 물을 흡착시킨다는 것을 확인하였다. 또한 계면의 용매, 용질 그리고 격자층의 확산계수를 분석한 결과 용매인 물이 "Roughening Transition" 메커니즘으로 결정성장에 영향을 준다는 것을 밝혔다.다는 것을 밝혔다.

• Applied Chemistry for Engineering
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• v.28 no.4
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• pp.420-426
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• 2017

Recently, solvent-resistant nanofiltration membranes have been studied for the separation of solvents or solutes using a molecular weight cut-off system of the polymer which is resistant to a specific solvent. Required conditions for these membranes must have are excellent physical properties and solvent resistance. Polybenzimidazole, which is known to be one of the most heat-resistant commercially available polymers, has an excellent inherent solvent resistance and it is even insoluble in stronger organic solvents when cross-linked. Therefore, in this study, the applicability of polybenzimidazole as a solvent resistant nanofiltration membrane was discussed. The membrane was fabricated using the non-solvent induced phase separation method and showed a suitable morphology as a nanofiltration membrane confirmed by field emission scanning electron microscopy. In addition, the permeance of the solvent in the presence or absence of cross-linking was investigated and the stability was also confirmed through long operation. The permeance test was carried out with five different solvents: water, ethanol, benzene, N, N-dimethylacetamide (DMAc) and n-methyl-2-pyrrolidone (NMP); each of the initial flux was $6500L/m^2h$ (water, 2 bar), $720L/m^2h$ (DMAc, 5 bar), $185L/m^2h$ (benzene, 5 bar), $132L/m^2h$ (NMP, 5 bar), $65L/m^2h$ (ethanol, 5 bar) and the pressure between 2 and 5 bar was applied depending on the type of membrane.

• Polymer(Korea)
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• v.36 no.4
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• pp.542-548
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• 2012

Morphological characteristics and formation of symmetric polystyrene-block-poly(1,4-butadiene) copolymer (PS-b-PBD) in thin films upon solvent-annealing were investigated by using atomic force microscopy (AFM). The thin films solvent-annealed in cyclohexane revealed the perforated lamellae of poly(1,4-butadiene) in the matrix of polystyrene while those solvent-annealed in n-hexane exhibited highly disordered patterns. Interestingly, when the thin films of PS-b-PBD were solvent-annealed with binary mixtures of cyclohexane and n-hexane, the morphological transition from the perforated lameallae to the perpendicularly-oriented lamellae of poly(1,4-butadiene) could be induced by changing the mixing ratio of both solvents. We also demonstrated that after microdomians of poly(1,4-butadiene) were successfully degraded by UV-$O_3$, linear poly(dimethyl siloxane) chains were back-filled into the etched regions of the thin film and then converted to silica nano-objects by oxygen plasma treatments.

• Korean Journal of Food Science and Technology
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• v.29 no.6
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• pp.1222-1227
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• 1997

Effects of the physical properties of solvent system such as pH and polarity change by salt addition in solvent system were investigated by using high speed countercurrent chromatography apparatus (Model CCC-1000, Pharm-Tech Research Corp. USA). The changes of pH and interfacial tension in solvent system of high speed countercurrent chromatography did not significantly affect on retention of stationary phase, but induced remarkable changes in the partition coefficient of ginkgo flavonoids, kaempferol, quercetin and isorhamnetin. The partition coefficients of ginkgo flavonoid standard increase with an increased pH of solvent system and quercetin sharply increased at pH 10.0. Retention of stationary phase decreases with an increased concentration of KCl in butanol of solvent system. Interfacial tension between two phase in solvent system of hexane increases with an increased concentration of KCl. The polarity of solvent system significantly changes the partition coefficients of ginkgo flavonoid.

• Resources Recycling
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• v.23 no.1
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• pp.48-57
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• 2014

In this study, we have investigated the influence of the nature of solvent on the grafting reaction of maleic anhydride onto polyethylene wax obtained as a by-product in a high density polyethylene plant. The results show that the grafting ratio in xylene as a solvent was higher than toluene. This is because xylene has excellent monomer solubility, swelling property and miscibility. It has been also observed that grafting degree shows an initial jump in percentage of grafting with increasing amount of solvent, from 0% v/w to 200% v/w giving maximum grafting in 200% v/w and then slightly decreases on further increase in the amount of solvent and becomes almost constant. It can be also seen that gel content was not formed under the use of solvent. It means that solvent prevented cross-linking reaction due to chain transfer reactions to solvent molecules. Studies of melt viscosity at $140^{\circ}C$ showed that viscosity increased after grafting of maleic anhydride onto polyethylene wax.

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.250.2-250.2
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• 2010

빛과 공기 중의 이산화탄소를 고정화하여 생성되는 바이오매스(biomass)로부터 다양한 에너지 및 물질을 생산하는 연구는 석유고갈과 환경문제 해결의 한 방안으로서 활발히 진행되어 왔으며, 앞으로도 그 지속 가능성과 환경 친화성에 의해 바이오에너지 이용 및 보급은 꾸준한 증가세를 보일 것으로 전망된다. 바이오디젤, 바이오에탄올의 경우는 미국, 브라질, EU, 한국 등에서 상용화되어 사용되고 있으며 그 생산량이 계속적으로 증가하고 있다. 하지만, 바이오연료의 보급 증가는 식량 자원과의 충돌과 열대우림 파괴 등의 부작용을 일으키고 있다. 이러한 문제 해결의 일환으로 단위면적당 생산성이 대두, 유채보다 월등한 것으로 보고되는 미세조류에 대한 관심이 증가하고 있으며 우수 미세조류종 개발, 미세조류 고속배양 및 수확, 미세조류로부터 에너지 및 유용물질, 소재 생산에 대한 연구가 활발히 진행되고 있다. 본 연구에서는 미세조류로부터 바이오디젤 원료유를 생산하기 위해 Soxhlet을 이용한 추출 방법을 이용하였다. 추출되는 오일은 사용 용매의 극성에 따라 물성과 추출 효율에 차이가 큰 것으로 나타났다. 강한 극성의 용매일 경우, 엽록소와 단백질이 같이 추출되는 문제가 있으며 약한 극성 용매는 세포벽의 방해로 용매가 세포내부로 흡수되지 못하는 문제가 있다. 추출 효율이 높은 극성용매의 경우 불순물을 제거해야 고순도의 바이오디젤의 생산이 가능하고 비극성 용매는 추출 오일의 물성은 좋으나 수율이 매우 낮게 측정되었다. 이러한 동시추출을 방지함과 동시에 추출 효율을 높이기 위해 본 연구에서는 세포벽 파괴 후 용매추출하는 방법으로서 미세조류를 Microwave에 노출시켜 오일 추출율을 증가시키는 전처리 연구를 수행하였다. 전처리시, Microwave에 의한 열 발생은 미세조류를 탄화시키기 때문에 열매체로서 물을 혼합하여 탄화를 방지하고 세포벽 내외부의 가열효과로 세포벽을 파괴하고자 하였다. Microwave에 의한 에너지 손실을 줄이며 세포벽 파괴에 효과적인 수분혼합비를 조사하였으며 Microwave에 노출 후 잔류수분을 건조하고 효율적으로 용매를 접촉시키기 위해 분쇄를 수행하였다. 모든 전처리 반응을 거친 미세조류에서 약 2배 증가된 추출수율을 얻을 수 있었으며, SEM을 통해 전처리 미세조류와 미전처리 미세조류를 분석해본 결과 전처리 미세조류의 다공성이 증가함을 확인하였다. 또한, 90%의 메탄올에 미세조류를 녹여 엽록소 함유량을 측정한 결과, 전처리 미세조류의 엽록소가 미전처리 미세조류보다 약 7배가량 감소함을 확인할 수 있었다.

• Analytical Science and Technology
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• v.6 no.5
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• pp.453-462
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• 1993

The retention behaviors of polystyrenes influenced by mixed solvents are examined in thermal field-flow fractionation(ThFFF). Experimental data are obtained with polystyrene samples of molecular weights of 35,000, 110,000, 200,000 and 470,000 dissolved in organic solvents. The pure and mixed solvents are tetrahydrofuran(THF), chloroform(CHL), cyclohexane(CH), and benzene(BZ), respectively. The values of retention ratio(R) and thermal diffusion coefficient($D_T$) are measured with change of molecular weight and composition of mixed solvents. Atempts are then made to correlate the measured values with various physicochemical parameters of polymers and solvents. Studies suggest that R is significantly increased with the density of solvent and a good correlation is found between them. $D_T$ values decreases in the mixed solvent having has a higher concentration of poor solvent.

• Journal of the Korean Chemical Society
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• v.38 no.3
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• pp.221-223
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• 1994

We tried to apply the linear solvation energy comparison method to solute retention in normal phase liquid chromatography. Correlation coefficients of regression of lnk' collected in a fixed eluent against solute polarity indices have proven to be lower than those obtained from reversed phase liquid chromatography data. This event can be attributed to complexity of solute retention process in normal phase liquid chromatography. We concluded from the regression results that each specific polarity of the stationary phase is greater than that of the mobile phase and that the difference in each polarity between the stationary phase and the mobile phase decreases as the volume fraction(${\phi}$) of the more polar solvent in the mobile phase increases. Correlations of lnk' of a single solute against solvent polarity indices have proven to be meaningless owing to covariance among the solvent polarity indices. Instead, a good linear relationship between lnk' and solvent ${\pi}^*$ was observed, and its linearity is better than that between lnk' and ${\phi}$.