• The Korean Journal of Rheology
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• v.5 no.2
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• pp.149-160
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• 1993

표면성장법을 이용한 고강력, 고탄성률 섬유의 제조시, 결정화 온도에 따른 섬유 미 세구조와 물리적 성질의 상관 관계를 미세구조적, 열역학적 관점에서 규명하고자 초고분자 량 폴리에틸렌으로 섬유를 제조하고 결정화 온도에 따른 구조와 인장 성질의 변화를 용융 거동을 중심으로 관찰하였다, 일정길이하에서의 섬유의 용융인 제한 용융에서는 고분자 사 슬배좌의 구속으로 인해 사방정계-육방정계 전이가 일어났다 제한 용융 거동으로부터 라멜 라 구조와 펼쳐진 사슬 결정 부분을 분리할 수 있었으며 결정화 온도가 증가할수록 펼쳐진 사슬 결정의 양이 증가하였다. 결정화 온도가 증가할수록 쉬시-케밥구조에서 펼쳐진 사슬 구조로의 변화가 일어났으며 결정내의 결점도 줄어들었다. 결정화 온도가 증가할수록 구조 의 변화로 인해 인장 성질이 향상되었다. 인장 성질은 펼쳐진 사슬 결정의 양에 큰 영향을 받았다. 인장 강도는 펼쳐진 사릉의 양과 사슬내의 결점들에 의해 큰 영향을 받았으며 인장 탄성계수와 절단 신도는 인장 강도보다 펼쳐진 사슬의 양에 더 크게 영향 받았다.

• Clean Technology
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• v.12 no.2
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• pp.95-100
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• 2006

Fractionation and hydrodealkylation (HDA) units, subparts of BTX plant, were thermodynamically analyzed using the notion of exergy. Exergy values were calculated as the sum of physical and chemical exergies due to the existence of chemical reactions. The analysis was based on the simulation results with the aid of real operating data. Driving and material exergy losses were separately defined and quantified. Locations and the reason of major exergy losses were identified and improvement strategies were suggested. It was noted that the exergy analysis could provide a sound base for adopting the concept of industrial ecology and developing loss prevention schemes.

• Journal of the Korean Chemical Society
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• v.50 no.3
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• pp.190-195
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• 2006

The critical micelle concentrations (CMC) and the counter ion binding constants (B) in a micellar state of the mixed surfactant systems of sodium dodecylbenzenesulfonate (DBS) with polyoxyethylene(4) lauryl ether (Brij 30) in water were determined as a function of 1 (the overall mole fraction of DBS) by the use of electric conductivity method and surface tensiometer method from 288 K to 308 K. Various thermodynamic parameters (Smo, Hmo, and Gmo) for the micellization of DBS/Brij 30 mixtures were calculated and analyzed from the temperature dependence of CMC values. The measured values of Gomare all negative but the values of Smo are positive in the whole measured temperature region. On the other hand, the values of Hmo are positive or negative, depending on the measured temperature and 1.

• Journal of the Korean Applied Science and Technology
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• v.36 no.2
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• pp.407-416
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• 2019

The criticical micelle concentration (CMC) was measured by using the UV-Vis method for the micellization of the ammonium type cationic surfactants (DTAB, TTAB, and CTAB) in the aqueous aniline solution. The enthalpy change (${\Delta}H^0$) and entropy change (${\Delta}S^0$) were calculated from the dependence of Gibbs free energy change (${\Delta}G^0$) on the temperature for micellization of the cationic surfactants between 290K and 314K. The effects of n-butanol and sodium chloride on the micellization of cationic surfactants were measured and compared with the other thermodynamic functions. All the free energy changes (${\Delta}G^0$) of the micellization were negative, all the enthalpy change (${\Delta}H^0$) were negative, and all the entropy change (${\Delta}S^0$) were positive values, respectively. The micelle formation of cationic surfactant in aniline solution is a spontaneous exothermic reaction, and the iso-structural temperature calculated from the thermodynamic values show that enthalpy and entropy contribution to the micellization are almost the same for the micellization of cationic surfactants

• Proceeding of EDISON Challenge
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• 2014.03a
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• pp.39-51
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• 2014

산성비의 주요 원인인 이산화황($SO_2$)을 배기가스로부터 효과적으로 제거하기 위한 용매 중 이온성 액체(ionic liquid, IL)의 $SO_2$ 흡수능 (absorption capacity)을 양자화학적 방법을 이용하여 평가했다. 이를 위해 hydroxyl ammonium 계열의 양이온 monoethanolammonium, diethanolammonium 2종과 carboxylate 계열의 음이온 acetate, formate 2종을 조합하여 총 4종의 IL을 연구에 적용했다. $SO_2$가 IL의 pair, 양이온 또는 음이온과 complex를 형성할 때로 구분하여 계산 모델을 세웠으며, 열역학적 상태 변화와 오비탈 상호작용 분석을 통해 흡수능을 평가하였다. 계산 결과, 음이온-$SO_2$ complex를 적용했을 때 formate에 비해 acetate가 $SO_2$ 흡수에 유리할 것으로 분석되었으며, 이는 이전의 실험 연구에서 얻어진 흡수능 경향성과도 잘 맞는다.

• Proceedings of the Membrane Society of Korea Conference
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• 1995.04a
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• pp.56-57
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• 1995

막반응기는 반응물이나 생성물을 선택적으로 분리함으로써 반응과 분리를 동시에 수행한다. 이러한 막반응기는 주로 열역학적인 평형에 의해 전화율이 제약되는 반응의 전화율을 높이기 위해서 연구되어 왔다. 수소의 저장 방법의 하나인 액상 하이드라이드법에서 저장된 수소를 다시 분리해 내기 위해 사용되는 사이클로헥산의 탈수소화 반응에 대해 많은 연구가 이루어졌다. 그러나 앞선 연구자들의 결과는 막의 투과도가 낮아서 반응기의 performance가 투과율에 의해 결정된다고 보고하였다. 본 연구에서는 막의 투과도와 촉매 양의 변화에 따른 사이클로헥산 탈수소화 반응의 전화율 변화를 전산모사함으로써, 최적 혹은 최대의 전화율을 나타내는 투과도 및 촉매 양을 결정하는 방법을 제시한다.

• Journal of the Korean Applied Science and Technology
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• v.36 no.4
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• pp.1143-1152
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• 2019

In order to study the solubilization of aniline by cationic surfactants (DTAB, TTAB and CTAB), the solubilization constant (K_s) and thermodynamic functions were measured and calculated by using the UV-Vis method. The solubilization constants of aniline with the change of temperature were measured, and the effects of addition of ionic salts and organics on the solubilization constants were investigated. These effects of additives and temperature changes were compared and analyzed for each type of surfactant, and the solubilization of aniline was analyzed microscopically by comparing and evaluating the thermodynamic functions obtained from the solubilization constants. As a result, the Gibbs free energy and enthalpy changes were both negative and the entropy changes were positive within the measured range for the solubilization of aniline by cationic surfactants. The solubilization constant value decreased with increasing temperature and increased with increasing carbon chain length of the surfactant. As the concentration of ionic salts increased, the Gibbs free energy change increased at first and then decreased. In n-butanol solution, the Gibbs free energy change tended to increase continuously with increasing the concentration of n-butanol.

• Membrane Journal
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• v.18 no.4
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• pp.317-324
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• 2008

Polysulfone membranes were prepared via the phase inversion process. With propionic acid as a nonsolvent additive, polysulfone casting solutions were solidified in an isopropanol bath. Propionic acid (PA) worked as a thermodynamic enhancer for phase separation and as a rheological suppressor for kinetic hindrance. Morphology of the prepared membranes significantly varied with propionic acid content in the casting solution. The dense skin layer, which was identified in the membrane prepared without PA, almost disappeared in the membrane prepared trom PA 10wt%. With 30wt% PA, the membrane revealed the morphological gradient from a nodular skin structure to a sponge-like substructure, including the finger-like cavity. Water permeability increased with PA content, and polyethylene glycol rejection decreased with the nonsolvent content.

• Journal of the Korean Chemical Society
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• v.26 no.5
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• pp.274-281
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• 1982

Ultraviolet spectrophotometric investigation have been carried out on the systems of pentamethylbenzene and hexamethylbenzene with iodine and iodine monochloride in carbon tetrachloride. The results reveal the formation of the one to one molecular complexes. The equilibrium constants were obtained in consideration of that absorption maxima due to the formation of the charge transfer complexes shift to blue with the increasing temperature. Thermodynamic parameters for the formation of the charge transfer complexes were calculated from these values. These results indicate that the complex formed between polymethylbenzene and iodine monochloride is more stable than that in the case of iodine. This may be a measure of their relative acidities toward polymethylbenzene, which is explained in terms of the relative electronegativities of halogen atoms. These results combined with previous studies of this series indicated that ${\lambda}_{max}$ shift to red with the increasing number of methyl groups on benezene ring and that the relative stabilities of these complexes increase in the order, Benzene < Toluene < Xylene < Durene < Mesitylene < Pentamethylbenzene < Hexamethylbenzene. The reason for the order found is thus additionally discussed.

• Polymer(Korea)
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• v.26 no.2
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• pp.245-252
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• 2002

Thermodynamics and gas transport properties of polymethylmethacrylate (PMMA) blends with polyvinylmethylether (PVME) containing various amount of poly (styrene-b-methylmethacrylate) copolymer (P(S-b-MMA)) as a compatibilizer were studied. To extract interaction energies of binary pairs involved in the blends from the phase separation temperatures using an equation-of-state theory, PVME blends with methylmethacrylate copolymers containing various amount of styrene (SMMA) were prepared. PVME formed miscible blends with methylmethacrylate copolymers containing more than 70 wt% styrene and these miscible blonds showed a LCST-type phase separation behavior. Based on the interaction information obtained here, P(S-b-MMA) copolymer was added to the PMMA/PVME blends to enhance their compatibility. The average diameter of the dispersed rubber particles was gradually decreased for the blends of containing P(S-b-MMA) from 0 to 5 phr and then leveled off at a fixed size. At a fixed bland composition, the gas permeation was also increased as the P(S-b-MMA) content increased from 0 to 5 phr and then leveled off when the P(S-b-MMA) content was higher than 5 phr.