• Korean Chemical Engineering Research
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• v.45 no.3
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• pp.209-214
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• 2007

Sr hexaaluminate($Sr_{1-x}La_xMnAl_{11}O_{19-\alpha}$) were prepared by sol-gel method of metal alkoxide with 1-butanol or ethylene glycol as a solvent. The physical properties of prepared hexaaluminates were examined by TG/DTA, XRD and $N_2$ adsorption. When ethylene glycol was used as a solvent, the decomposition reaction and dehydroxylation reaction was observed above $400^{\circ}C$ and the temperature of the formation of a crystal structure of hexaaluminate was also increased resulting in small specific surface area and low catalytic activity of methane compared to Sr-hexaaluminate with 1-butanol.

• Korean Journal of Environmental Agriculture
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• v.11 no.2
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• pp.146-154
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• 1992

DDVP, malathion and diazinon ECs which differ in chemical compositions and moisture contents were formulated with nine emulsifiers, three solvents(xylene, cyclohexanone and DMF) and epichlorohydrin. For the studies of decomposition characteristics, these technicals and ECs were subjected to the test under elevated temperature at $54^{\circ}C$ for 15 days and $38^{\circ}C$ for 90 days respectively. DDVP technical was rapidly decomposed in early stage of thermoaccelerated test at $54^{\circ}C$, but the decomposition rate slowed down with time. As for malathion and diazinon technicals, the longer they were incubated, the more decomposed. The decomposed AI in ECs increased with solvent polarity. The increment of moisture content in ECs accelerated the decomposition of AI, and that was remarkable especially in diazinon ECs. Addition of emulsifiers increased the moisture content to be accelerated the decomposition of AI, but the decomposition of AI was more affected by the kind of emulsifier than by the moisture content of emulsifier, Stabilizing effect by epichlorohydrin was distingished in malathion and diazinon ECs, but there was no effect in other solvent-based formulation except xylene.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.03a
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• pp.64-64
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• 2011

모발(human hair)은 양모섬유와 마찬가지로 시스틴을 많이 함유하고 있는 섬유상 케라틴 단백질로써, 두부(頭部)를 보호할 뿐만아니라 신체에 필요하지 않는 중금속을 체외로 방출하는 기능을 지닌 신체의 일부분이다. 또한 모발은 미(美)와 관련하여 가장 관심을 가지는 부분이며, 다양한 방법으로 모발에 변화를 주어 신분을 표시하거나 자신의 미적 표현을 하고 있다. 퍼머넌트 웨이브는 모발에 형태학적 변화를 주는 유효한 수단이며, 염색과 탈색 등은 색상 변화를 주는 중요한 수단이다. 본 연구 에서는 모발을 산성염료로 염색할 때 염색성을 향상시키기 위하여 염색보조제로써 벤질알콜 등을 첨가하여 염색할 때 염색된 모발의 염착량, 보습성, 단백질 유출성, 주사전자 현미경 관찰을 측정하여 다음과 같은 결과를 얻었다. 1) 염색시간이 길어지고, 염색온도가 높아질수록 모발에의 염착량은 증가하며, 특히 벤질 알콜을 첨가하여 염색하는 경우에는 빠른 시간내에 염착평형에 도달하고 비교적 낮은 염색온도에서도 높은 염착량을 나타내었다. 2) 이와같은 용매 첨가의 효과는 염액에 계면활성제와 함께 첨가하여 염색하면 나타나지 않았다. 3) 염색시간이 길어질수록 모발의 보습성은 열악해지지만, 벤질 알콜을 첨가하여 염색하는 경우에는 오히려 보습성이 증가하였다. 또한 염색시간이 길어지면 모발의 단백질 유출성은 증가하지만, 벤질 알콜을 첨가하여 염색하는 경우에는 오히려 단백질 유출성이 감소하였다. 이와같은 결과는 벤질 알콜을 첨가하여 염색하는 경우에 모발의 손상이 적다는 것을 의미한다. 4) 모발의 손상정도에 대한 주사전자현미경의 측정결과는 벤질 알콜의 첨가여부에 따라 큰 차이를 보이지 않았다.

• Proceedings of the Korean Printing Society Conference
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• 1995.11a
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• pp.13-17
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• 1995

헤테로원자(X=O, S, Se)의 변환에 따라 용액상에서 Merocyanine색소 및 Cyanine색소의 헤테로원자X는 p궤도의 원자보다 d궤도의 원자가 공명에 관여하여 공역계확장에 기여하였고, 유전률이 큰 용매 일수륵 Merocyanine색소는 장파장으로 흡수극대치가 이동하였다. 또 Cyanine색소의 기저상태는 $I^-$이온과 정전하 발색단을 가진 이온성 화합물로 되어 있으므로 극성용매에서 $I^-$ 이온의 전하가 색소본체로 전하 이동전이가 발생하여 단파장화 하였다. 고상에서 색소의 농도가 높을 수록 색소분자간의 거리가 가까워져 색소 상호작용이 변화하여 흡수스펙트럼에서는 전체적으로 폭이 넓은 형태로 나타났으며 이것은 농도가 높을 수록 색소분자간의 거리가 가까워져 색소 상호작용이 변화한 때문이라고 생각된다. 또한 3차원 형광의 저농도에서 보이지 않는 새로운 스펙트럼이 Cyanine색소에서 나타났으며 이 스펙트럼은 색소고유의 흡수에 기인한 것으로 Eximer형광으로 생각된다. 광전특성에 있어서는 Merocyanine색소가 Cyanine색소보다 활성화에너지가 낮아 전하이동도가 커짐에 따라 높은 광전특성을 나타내었다. 그리고 Merocyanine색소 헤테로원자(X)의 비교에서 광전특성은 O

• Proceeding of EDISON Challenge
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• 2015.03a
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• pp.117-123
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• 2015

본 연구에서는 DFT를 이용하여 Nucleophilicity와 Basicity의 연관성에 대한 계산화학적 분석을 수행하였다. Basicity는 선정된 모델 분자의 protonation 반응에서 생성물과 반응물의 enthalpy 변화량인 양성자 친화도(Proton affinity, PA) 값을 구하여 분석하였다. 계산한 결과는 실험을 통해 얻은 PA 결과와 경향성이 거의 일치함을 확인하였다. Nucleophilicity는 모델 분자들과 $CH_3Br$ (electrophile)의 $SN_2$반응에서 gibbs free energy of activation(${\Delta}G^{\ddag}$) 값으로 그 경향성을 분석하였다. 또한 용매의 종류를 다르게 하여 용매에 따른 ${\Delta}G^{\ddag}$ 값의 경향성도 확인하였다. 각 용매에 따라 구한 ${\Delta}G^{\ddag}$와 PA의 상관관계를 비교하였으나, 큰 연관성은 보이지 않았다. 이에 ${\Delta}G^{\ddag}$와 PA의 상관관계를 보여줄 수 있는 parameter를 찾기 위하여 각 모델 분자의 Electronegativity와 Polarizability를 계산하여 연관성을 비교해보았다. Polarizability를 적용했을 때 Nucleophilicity와 Basicity사이의 연관성을 나타낼 수 없었던 반면, Electronegativity를 적용하여 Basicity와 Nucleophilicity의 연관성 보일 수 있음을 이론적으로 규명하였다.

• Proceedings of the Membrane Society of Korea Conference
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• 1994.10a
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• pp.42-45
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• 1994

정밀화학, 제약산업 등에 필요한 에탄올, IPA 등과 같은 유기용매를 고순도로 농축하는 공정은 유기용매와 물과의 혼합물이 일정 농도에서 공비점을 형성하여 일반 증류로는 분리하기 힘들어 Benzene, Cycloheaxane 드의 Entrainer를 첨가하여 상대휘발도를 변화시켜 분리하는 공비증류가 이용되고 있다. 그러나 공비증류는 에너지 사용량이 많고 유독한 물질을 사용하므로 투과증발법과 같은 저에너지 소비형, 환경 친화적인 공정에 대한 관심이 높아지고 있다. 투과증발법에 의한 유기용매 농축공정은 물과의 친화성이 높은 비다공성 막을 이용하여 선택적으로 물을 투과하여 유기용매를 탈수하는 방법으로 투과를 위한 Driving force는 Feed side와 Permeate side사이의 Chemical potential gradient로 이는 물에 대한 Partial vapor pressure differnece로 다음과 같이 표시된다. $\Delta \mu_{F/P.W} = RT ln\frac{y_WP_P}{x_W\gamma_WP_{o.W}}$ 따라서 투과속도를 높이기 위해서 Permeate side를 진공상태로 하여 투과하는 물질을 기화시키고 이를 다시 응축하여 Permeate side의 압력을 낮게 유지시켜야 한다.

• Journal of the Korean Applied Science and Technology
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• v.38 no.1
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• pp.292-299
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• 2021

In this study, a study was attempted to confirm the yield of the solvent fraction for extracting physiologically active substances of polyphenols and flavonoids in sea cucumber. In the previously reported cases, the 50% ethanol extraction solvent fraction was confirmed as a result of high yield of sea cucumber antioxidants. The determination of the amount of antioxidants extracted from sea cucumber was confirmed as a result of the extraction solvent fraction applied to the extraction. In addition, the necessity of extraction of the solvent fraction was obtained through a previous study that 'there is a significant difference in the content of sea cucumber physiologically active antioxidants extracted depending on the extraction solvent.' The results of extracting high antioxidants from the phenolic substances contained in the sea cucumber extract of the 50% ethanol extraction solvent fraction were demonstrated. In the study case of extraction solvent fraction, the ethyl acetate solvent fraction, which yielded the lowest, yielded a higher phenol content than other solvent fractions, and the antioxidant effect was confirmed. Accordingly, it was confirmed that the effect on the high yield of the antioxidant extract through the yield change according to the application of the extraction solvent fraction was performed. Therefore, it was verified as an optimized sea cucumber physiologically active substance extraction solvent fraction of 50% ethanol solvent.

• Polymer(Korea)
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• v.26 no.3
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• pp.307-315
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• 2002

Major factors affecting the impact resistance of high impact polystyrene (HIPS), the rubber-toughened grade of polystyrene, are rubber-phase particle size and size distribution, molecular weight, morphology, and degree of grafting. Accordingly, it is important to control or investigate these factors. In this study, the effect of solvent content was analyzed by the morphology and particle size distribution of rubber phase, and final properties in bulk-solution polymerization of HIPS. The prepolymerization time was, first, determined by measuring the evolution of particle size distribution of dispersed phase to explain the phase inversion with time. As the solvent content increased, the size of rubber particle increased and then gradually decreased. Rubber-phase morphology was likely to have higher degree of grafting as the solvent content increased. Rheological and mechanical properties decreased as the solvent content increased because of the decrease of matrix molecular weight due to the chain transfer reaction to solvent and the existence of residual solvent. Nevertheless, the impact resistance seemed to increase when the rubber particle size increased.

• Applied Chemistry for Engineering
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• v.8 no.6
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• pp.967-972
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• 1997

Recovery of aromatics in extract phase which was obtained by batch equilibrium extraction between light cycle oil(LCO) and dimethylsulfoxide(DMSO) solution as solvent was investigated by re-extraction. To select the most suitable re-extraction solvent for recovery of aromatics in extract phase, distribution equilibrium was measured between extract phase and solvents. The solvents used were benzene(B), toluene(T), m-Xylene(mX), n-hexane(Hx) and n-hexane(Hx) and n-Octane(Ot). From the distribution coefficients and yields of aromatics, Hx seemed to be the most suitable. Furthermore, effects of operation parameters for re-extraction of aromatics in the extract phase were studied by batch equilibrium re-extracion with Hx as solvent. Yields of aromatics were found to increase with increasing solvent/feed (extract phase) mass ratio(S/F), while distribution coefficients of aromatics were fixed irrespective of S/F used. Operating temperature did not affect distribution coefficients and yields of aromatics. Distibution coefficients and yields of naphthalene group(carbon numer : 10~12) increased with increasing cabon number. Mass transfer rates of aromatics were also measured with a batch stirred vessel.

• Journal of the Korean Chemical Society
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• v.34 no.6
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• pp.509-516
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• 1990

1H-nmr chemical shifts and lineshapes of amino-protons of acetamide (AA) in n-alcohols were determined. The chemical shifts are discussed by the Reichardt's solvent polarity parameter, E$_{T}$(30). The following relationship between $\delta$obs and E$_{T}$(30) was obtained. ${\delta}_{obs}$ = ${\delta}_{o}$ ＋ aE$_{T}$ (30) ＋ b[E$_{T}$(30)]$^2$ where ${\delta}_{o}$ is the chemical shift of the solute in gaseous state or at $E_{T}$(30) = 0, a is a characteristic constant for the protons of AA in n-alcohol solutions and b is a constant for the solute (AA)-solvent (n-alcohols) interaction. The barrier of the hindered rotation about the N-C(O) bond in AA was obtained by analysis of the lineshapes of the amino-protons in AA. The behavior of the internal rotation as well as chemical shifts of the amino-protons in AA has been found to be closely related to the $E_{T}$(30) of n-alcohols.