• Journal of the Korean Society of Marine Environment & Safety
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• v.13 no.4
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• pp.51-54
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• 2007

Surfactants can be used as a cosmetics and chemical dispersants. The variation of critical micelle concentration(CMC) with temperature for hexadecyl pyridinium bromide over the range $40^{\circ}C$ to $60^{\circ}C$ has been measured by drop methods. Thermodynamic quantities for micellization of hexadecyl pyridinium bromide in water have been calculated by polynominal equation.

• Journal of the Korean Chemical Society
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• v.37 no.6
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• pp.562-569
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• 1993

The pseudophase separation model is used to describe the effects of pH and n-propanol on the mixed micellar formation of protonated and unprotonated dimethyldodecylamine oxides. Dimethyl-dodecylamine oxide surfactant molecules may exist in aqueous solution in either nonionic (unprotonated) or cationic (protonated) form, and they can be modeled thermodynamically as a binary mixture of cationic and nonionic surfactants. The composition of the binary mixture is varied by adjusting the solution pH. And activities, micellar compositions, and monomeric compositions of two surfactant species can be calculated directly from the experimental titration data by applying pseudophase separation model to the micellar system of DDAO in water/n-propanol. The critical micellar concentrations and the p$K_a$ values of the binary mixture systems are dependent on the micellar composition of the protonated cationic surfactant (X); especially they show the minimum phenomena when they are plotted against the micellar composition of the protonated cationic surfactant (X). The critical micellar concentration of the binary mixed DDAO system is generally decreased when n-propanol is added to the binary mixture system, and the degree of decrease is dependent on the concentration of n-propanol.

• Journal of the Korean Society of Marine Environment & Safety
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• v.14 no.2
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• pp.145-148
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• 2008

Cationic surfactant can be used as cosmetics and chemical dispersants. The variation of critical micelle concentration (CMC) with temperature over the range $40^{\circ}C$ to $60^{\circ}C$ for N-octadecyl pyridinium bromide was measured by drop methods. Thermodynamic quantities such as free energy, enthalpy, entropy and heat capacity for micellization of N-octadecyl pyridinium bromide in water were calculated by fourth-degree polynominal equation In the result, free energy change was decreased generally by the increment of temperature.

• Journal of the Korean Chemical Society
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• v.59 no.4
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• pp.271-279
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• 2015

The critical micelle concentration (CMC), the counter ion binding constant (B) and the aggregation number (N^* ) for the mixed micellization of sodium dodecanoate and sodium n-octanoate as two anionic surfactants have been investigated by means of electric conductivity and light scattering. As its experimental results are found to be deviated from ideal mixed model, thus two different kinds of regular solution models such as Rubingh and Motomura are used for interpreting our experimental data. The stability of the mixed micelles has been confirmed from the negative values of the standard Gibbs energy of mixed micellization ΔG^micel,0 over all compositions and the measured values of ΔG^micel,0 agreed with the theoretical ones within the experimental error.

• Journal of the Korean Chemical Society
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• v.55 no.2
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• pp.163-168
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• 2011

The variations of molar conductivity of various surfactants such as sodium caprylate, sodium laurate, sodium palmitate, sodium stearate, sodium oleate, sodium dodecyl sulphate, and lithium dodecyl sulphate with concentrations of the surfactants for each of the solutions consisting of mixtures of varying concentrations of N-methyl acetamide in water at constant temperature of $30{\pm}0.2^{\circ}C$ were studied. The critical micelle concentration (CMC) for each surfactant is measured. It is found that the CMC values in mixtures of N-methyl acetamide and water solutions of various surfactants are lower than the CMC values in water, and the driving force for micelle formation correlates with solvophobicity. The surfactant-solvent interactions that drive amphiphilic self-organization in N-methyl acetamide in water are discussed. Thermodynamic parameters were evaluated for micellar system to explain the results.

• Journal of the Korean Chemical Society
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• v.36 no.1
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• pp.28-32
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• 1992

The critical micelle concentration(CMC) values of Dodecylpyridinium bromide(DoPB) were determined by an electric conductivity method at 1${\sim}$2000 bars and $25^{\circ}C$. The CMC of DoPB increases with the addition of urea in the whole pressure region studied, and the CMC increases with an increase of the pressure in the low-pressure region, while in the high-pressure region the CMC decreases. The partial molar volume change $({\Delta}V^m_o)$ on micellization was also investigated in some urea aqueous solutions. The change $({\Delta}V^m_o)$ was reduced by the addition of urea. The results suggest that the "iceberg" structure of water around the hydrocarbon chain of the monomeric surfactant is effectively broken down by urea.

• Proceedings of the Membrane Society of Korea Conference
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• 1995.10a
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• pp.29-30
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• 1995

산업폐수는 종종 희석용액 내에 많은 유독성 물질을 함유하고 있다. 산업폐수를 처리하는 분리공정으로 역삼투막과 한외여과와 같은 막분리 기술은 분리 공정이 간단하고 상변화없이 폐수용량을 크게 감소시킬 수 있고 에너지 소모가 작은 장점을 가지고 있어 그 적용이 확산되고 있다. 계면활성제의 흡착성을 이용한 한외여과 막분리는 높은 막투과속도와 계면활성제의 높은 선택성이 결합된 것인데, Sodium Dodecyl Sulfate(SDS)와 같은 계면활성제를 이용하여 폐수로부터 불용성 중금속 이온과 독성의 유기물질을 분리하는 데에 적용할 수 있다. 임계미셀농도(CMC) 이상에서의 농도에서, 60~200 계면활성제 분자들이 거대분자나 미셀을 형성하면서 서로 응집된다. 그러므로 음으로 하전된 미셀과 결합된 금속 음이온은 2,000에서 10,000 범위의 분자량을 가지는데 역삼투막(RO)보다 작은 압력에서 상당히 큰 막투과속도를 가진 한외여과막에 의해 선택적으로 제거될 수 있다 본 연구의 목적은 중공사 한외여과막의 막투과속도에 미치는 인자들의 영향과, 계면활성제의 흡착성을 이용한 중공사 한외여과 막분리계 성능에 미치는 금속의 형태, S/M 몰비등의 효과를 결정하는데 있다.

• Applied Chemistry for Engineering
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• v.7 no.1
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• pp.109-117
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• 1996

Removal of metal ions on the ultrafiltration membrane with micellar-enhanced with anion surfactants is a recently developed technique which can remove heavy metals and small molecular weight ions from wastewater with simple separation process and without a phase change. Above a certain concentration, so called the critical micelle con binding cationic cobalt ions and anionic surfactants, were removed by ultrafiltration membrane. The transmembrane pressure difference had a relatively small effect on the rejection coefficient of metal ions on the ultrafiltration membrane whereas the level of anionic surfactant-to-metal ratio (S/M) had a substantial effect.

• Polymer(Korea)
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• v.33 no.2
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• pp.137-143
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• 2009

We prepared norfloxacin (NFX)-incorporated polymeric micelle using poly ($\varepsilon$-caprolactone)/poly(ethylene glycol) (PCL/PEG, CE) diblock copolymers. Particle size was from 60 to 200 nm according to the PCL block length. Their critical association concentration (CAC) was decreased according to the increase of PCL block length. $^1H$-NMR study showed core-shell type micelle structures of CE diblock copolymers in the aqueous environment. Drug release from polymeric micelle was continued over 2 days. Duration of drug release was varied according to the PCL block length and drug contents. At antimicrobial activity test, polymeric micelle showed almost similar cytotoxicity compared to NFX itself.

• Polymer(Korea)
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• v.30 no.6
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• pp.512-518
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• 2006

A biodegradable polymer poly((R) -3-hydroxybutyric acid) (PHB) was conjugated with a hydrophilic polymer poly(ethylene glycol) (PEG) by the ttansesterification reaction to form the amphiphilic block copolymer. PHB with low molecular weight ($3000{\sim}30000$) was appropriated for the drug delivery materials. High molecular weight PHB was hydrolyzed by an acid-catalyst to produce the low molecular weight one. Amphiphilic block copolymer was formed the self-assembled polymeric micelle system in the aqueous solution that the hydrophillic PEG was wraped the hydrophobic PHB. Generally, polymeric micelle forms the small particle between $10{\sim}200nm$. These polymeric micelle systems have been widely used for the drug delivery systems because they were biodegradable, biocompatible, non-toxic and patient compliant. The hydroxyl group of PEG was substituted with carboxyl group which has the reactivity to the ester group of PHB. Amphiphilic block copolymer was conjugated between PHB, and modified PEG at $176^{\circ}C$ which was higher than the melting point of PHB. Transesterification reaction was verified with DSC, FTIR, $^1H-NMR$. In the aqueous solution, critical micelle concentration (CMC) of the mPEG-co-PHB copolymer measured by the fluororescence scanning spectrometer was $5{\times}10^{-5}g/L$. The shape and size of the nanoparticle was taken by dynamic light scattering and atomic force microscopy. The size of the nanoparticle was about 130 nm and the shape was spherical. Our polymeric micelle system can be used as the passive targeting drug delivery system.