• Korea-Australia Rheology Journal
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• 제14권3호
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• pp.129-138
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• 2002

A cationic surfactant, cetyltrimethylammonium $\rho$-toluenesufonate (CTA$\rho$TS), forms long threadlike micelles in aqueous solution. The threadlike micelles make concentrated entanglement networks, so that the solution shows pronounced viscoelastic behavior as concentrated polymer systems do. However, a mechanism for a process responsible for the longest relaxation time of the threadlike micellar system is different from that of semi-dilute to concentrated polymer systems. The threadlike micellar system exhibits unique viscoelasticity described by a Maxwell model. The longest relaxation time of the threadlike micellar system is not a function of the concentration of CTA$\rho$TS, but changes with that of $\rho$-toluenesufonate ($\rho$$TS^{-}$) ions in the bulk aqueous phase supplied by adding sodium $\rho$-toluenesulfonate (NapTS). The rates of molecular motions in the threadlike micelles are not influenced by the concentration of $\rho$$TS^{-}$ anions, therefore, molecular motions in the threadlike micelles (micro-dynamics) are independent of the longest relaxation mechanism (macro-dynamics). A nonionic surfactant, oleyldimethylamineoxide (ODAO), forms long threadlike micelles in aqueous solution without any additives. The aqueous threadlike micellar system of ODAO also shows Maxwell type viscoelastic behavior. However, the relaxation mechanism for the longest relaxation process in the system should be different from that in the threadlike micellar systems of CTA$\rho$TS, since the system of ODAO does not contain additive anions. Because increase in the average degree of protonation of head groups of ODAO molecules in micelles due to adding hydrogen bromide causes the relaxation time remarkably longer, changes in micro-structure and micro-dynamics in the threadlike micelle are closely related to macro-dynamics in contrast with the threadlike micellar system of CTA$\rho$TS.

• 상하수도학회지
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• 제25권3호
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• pp.359-366
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• 2011

The feasibility of using volcanic ash for lead ion removal from wastewater was evaluated. The adsorption experiments were carried out in batch tests using volcanic ash that was treated with either NaOH or HCl prior to the use. Volcanic ash dose, temperature and initial Pb(II) concentration were chosen as 3 operational variables for a $2^3$ factorial design. Ash dose and concentration were found to be significant factors affecting Pb(II) adsorption. The removal of Pb(II) was enhanced with increasing volcanic ash dose and with decreasing the initial Pb(II) concentration. Pb(II) adsorption on the volcanic ash surface was spontaneous reaction and favored at high temperatures. Calculation of Gibb's free energy indicated that the adsorption was endothermic reaction. The equilibrium parameters were determined by fitting the Langmuir and Freundlich isotherms, and Langmuir model better fitted to the data than Freundlich model. BTV(base-treated volcanic ash) showed the maximum adsorption capacity($Q_{max}$) of 47.39mg/g. A pseudo second-order kinetic model was fitted to the data and the calculated $q_e$ values from the kinetic model were found close to the values obtained from the equilibrium experiments. The results of this study provided useful information about the adsorption characteristics of volcanic ash for Pb(II) removal from aqueous solution.

• 한국환경과학회지
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• 제27권6호
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• pp.401-410
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• 2018

Waste citrus peel-based activated carbon (WCAC) was prepared from waste citrus peels by activation with KOH. The removal of Cu and Pb ions from aqueous solution by the prepared WCAC was investigated in batch experiments. The solution pH significantly influenced Cu and Pb adsorption capacity and the optimum pH was 4 to 6. The adsorption of Cu and Pb ions by WCAC followed pseudo-second-order kinetics and the Langmuir isotherm model. The maximum adsorption capacity calculated by Langmuir isotherm model was 31.91 mg/g for Cu and 92.22 mg/g for Pb. As the temperature was increased from 303 K to 323 K, the ${\Delta}G^{\circ}$ value decreased from -7.01 to -8.57 kJ/mol for Cu ions and from -0.87 to -2.06 kJ/mol for Pb ions. These results indicated that the adsorption of Cu and Pb by WCAC is a spontaneous process.

• 한국전산유체공학회:학술대회논문집
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• 한국전산유체공학회 2008년도 학술대회
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• pp.208-214
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• 2008

The equilibrium molecular-dynamic simulations have been performed to estimate the properties of the three kinds of fluids (the Lennard-Jones fluid, water and aqueous sodium-chloride solution) confined between two plates that are separated by 1.086 nm; included in the equilibrium properties are the density distribution and the static structure, and the diffusivity in the dynamic property. Three kinds of fluids considered in this study are. The water molecules are modeled by using the SPC/E model and the ions by the charged Lennard-Jones particle model. To treat the water molecules, we combined the quaternion coordinates with Euler angles. We also proposed a plausible algorithm to assign the initial position and direction of molecules. The influence of polarization of water molecules as well as the presence of ions in the solution on the properties will be addressed in this study. In addition, we performed the non-equilibrium molecular-dynamic simulation to compute the flow velocity for the case with the gravitational force acting on molecules.

• 한국전산유체공학회:학술대회논문집
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• 한국전산유체공학회 2008년 추계학술대회논문집
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• pp.208-214
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• 2008

The equilibrium molecular-dynamic simulations have been performed to estimate the properties of the three kinds of fluids (the Lennard-Jones fluid, water and aqueous sodium-chloride solution) confined between two plates that are separated by 1.086 nm; included in the equilibrium properties are the density distribution and the static structure, and the diffusivity in the dynamic property. Three kinds of fluids considered in this study are. The water molecules are modeled by using the SPC/E model and the ions by the charged Lennard-Jones particle model. To treat the water molecules, we combined the quaternion coordinates with Euler angles. We also proposed a plausible algorithm to assign the initial position and direction of molecules. The influence of polarization of water molecules as well as the presence of ions in the solution on the properties will be addressed in this study. In addition, we performed the non-equilibrium molecular-dynamic simulation to compute the flow velocity for the case with the gravitational force acting on molecules.

• Carbon letters
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• 제9권1호
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• pp.8-16
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• 2008

Oxidized activated carbons were prepared by reacting steam-activated carbon developed from pecan shells with nitric acid of varying strength (15, 30, 45 and 60%). The textural properties and the chemistry of the surface of the non-oxidized and of the oxidized carbons were determined from nitrogen adsorption and base neutralization capacities. The uptake of Pb(II) and Cd(II) from aqueous solution by these carbons was determined by kinetic and equilibrium experiments as well as by the column method. Treatment with nitric acid brought about drastic decrease in surface area and remarkable increase in the pore size of the carbon with these changes depending on the strength of nitric acid. Nitric acid increased the surface acidity by developing new surface oxygen functional groups of acidic nature. $HNO_3$-oxidized carbons exhibited high adsorption capacities for Pb(II) and Cd(II). The adsorption of these ions increased with the decrease of the surface pH of the carbon and with the increase of the solution pH from 2.5 to 6 and 7. The amount adsorbed from lead and cadmium was also related to the amount of surface acidity, the pH of the point of zero charge and on some metal ion parameters. Cadmium and lead uptake by the investigated carbons followed pseudo-second order model and the equilibrium sorption data fitted Langmuir adsorption model.

• 한국물환경학회지
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• 제32권2호
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• pp.216-221
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• 2016

The adsorption characteristics of mixed heavy metals (Cr(III), As(VI)) in aqueous solution were investigated using a sediment amendment composite. Sediment amendment composite was composed of clean sediment (40%), zeolite (20%), recycled aggregate (10%), steel slag (10%), oyster shell (10%), and cement (10%). The experimental results showed that the adsorption equilibrium was attained after 180 mins. Heavy metal adsorption was characterized using Freundlich and Langmuir equations. The equilibrium adsorption data for the sediment amendment composite better fitted with the Langmuir model than the Freundlich model. The maximum adsorption capacity of Cr(VI) (36.07 mg/g) was higher than As(III) (25.54 mg/g); and the adsorption efficiency of the Cr(VI) and As(III) ions solution decreased with decreasing pH from 2 to 10. The collective results suggested that the sediment amendment composite is a promising material for a reactive cap that controls the release of Cr(VI) and As(III) from contaminated sediments.

• 산업기술연구
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• 제22권A호
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• pp.241-248
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• 2002

In this work, we calculated the vapor-liquid equilibrium of aqueous polymer solutions by using PRSV equation of state combined with $G^{ex}$ mixing rules(HVO, MHVL, MHV2, LCVM). From the comparison of calculated results with experimental data obtained from literature, we found that calculation results by using MHV1 mixing rule have showed small range of error than HVO, MHV2 and LCVM mixing rules. Calculation results by using the combination of MHV1 mixing rule and UNIFAC-FV model have showed the best result for selected aqueous polymer solutions.

• 설비공학논문집
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• 제9권2호
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• pp.144-152
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• 1997

Film absorption involves simultaneous heat and mass transfer in the vapor-liquid system. In the present work, the absorption process of water vapor by an aqueous soluton of LiBr flowing inside of the vertical tube was investigated. The continuity, momentum, energy and diffusion equations for the solution film and vapor were formulated in integral forms and solved numerically. The model could predict the film thickness, the pressure gradient, and the heat and mass transfer rate. Particularly the effects of vapor flow conditions on the absorption process were investigated in terms of the vapor Reynolds number. As the vapor Reynolds number increased, the shear stress at the vapor-solution interface also increased. Consequently solution film became thinner at higher vapor flowrate under the co-currentflow condition. Thinner film was capable of higher heat transfer to the wall and leaded to higher absorption rate of the water vapor into the solution film.

• 한국환경농학회지
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• 제38권2호
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• pp.83-88
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• 2019

본 연구는 미세플라스틱 주요물질 중의 하나인 PP와 담수상태에서 중금속 사이의 상관관계를 평가하기 위해 등온흡착모델과 다양한 흡착조건하에서 microplastic인 PP에 의한 Cd의 흡착특성을 평가하였다. Microplastic인 PP에 의한 Cd의 흡착경향은 Freundlich 흡착식에 적합하였으며, 주요한 흡착메카니즘은 물리적인 흡착으로 판단된다. 특히, PP에 의한 Cd의 흡착량은 반응시간과 반응온도에 지배적인 영향을 받았으며, 반응시간과 반응온도가 증가할수록 흡착량은 증가하였다. 초기 pH에 따른 흡착결과 PP에 의한 Cd의 흡착은 표면전하와 큰 상관관계가 없었고, FTIR분석을 통한 Cd 흡착 전과 후의 PP작용기에 별 다른 차이가 없어 PP에 의한 Cd의 흡착은 대부분 물리적 흡착으로 판단되었다. 결론적으로 담수상태에서 미세플라스틱인 PP는 Cd과 같은 중금속을 흡착한 후 생물체내로 이동시킬 수 있는 가능성을 확인할 수 있었고, 향후 미세플라스틱에 의한 중금속과 같은 독성물질이동과 전이매개체의 역할과 메커니즘을 규명하기 위한 체계적인 후속연구가 수행되어야 할 것으로 판단된다.