The diffusion behavior of phenol, toluene and benzoic acid in aqueous SDS solution was examined. It showed a similar experimental results for phenol and toluene. The diffusion coefficients of the solutes were characterized by the presence of two distinct regions: below the cmc and above the cmc. For phenol and toluene, it remained approximately unchanged when the SDS concentration was below the cmc. Above the cmc there was an apparent decrease in the diffusion coefficients of the two solutes with increasing SDS concentration. However, for benzoic acid the diffusion behavior was different from that of phenol and toluene. The diffusion coefficient of benzoic acid decreased slightly with increasing SDS concentration, however the diffusion coefficient was almost constant above the cmc. For benzoic acid the diffusion behavior was dependent on the joint contribution of benzoic acid molecules as well as the benzoate ions.

The interaction between anion and zwitterionic surfactants was investigated by means of surface tension, NMR spectroscopy, and fluorescence studies. These systems are N-tetradecyloxymethyl-N,N-dimethyl betaine (C14, TDB), N-octadecyloxymethyl-N,Ndimethyl betaine (C18, ODB), and sodium dodecylethoxy sulfate (SDE). These systems show a composition dependency in micellar properties. When the molar fraction of TDB and ODB was about 0.6, the cmc values of these systems showed minima, whereas the solubilized amount of a water insoluble dye, NMR line width showed maxima. These changes comes from the intramolecular complexes formed in the mixed micelles. The complexes are due to the electrostatic interaction of oppositely charged head groups of betaine and sodium dodecylethoxy sulfate. A comparison of betaine and SDE alkyl methylene group line widths to those of n-methyl group indicates that the interior of the micelle in the restricted region is more immobile than the head group.

Density, viscosity, conductance, dye solubility and carbon-13 nmr studies were performed in aqueous solution of three disodium 4-n-alkyl-3-sulfonatosuccinate anionic surfactant at 20℃. The cmc values were 0.14 mol/l for the disodium-4-n-octyl-3-sulfonatosuccinate(R8)S), 0.041mol/l for the disodium-4-n-decyl-3-sulfonatosuccinate(R10S), and 0.018mol/l for the disodium-n-dodecyl-3-sulfonatosuccinate 〈R12S). The aggregation numbers determined viscometrically and conductimetrically were 28 for R8S, 48 for R10S, and 67 for R12S. The volume changes upon micellization were 8.9cm3/mol for R8S, 9.5cm3/mol for R10S, and 10.1cm3/mol for R12S. Binding constants for the dye pada to the micelles and the fractions of unbound counter-ion were also obtained. The two polar heads with their carbon linkage were likely in an aqueous environment in the R8S micelles with the micelles themselves being spherical.

Sophorolipids were biosynthesized using a strain of yeast, Torulopsis bombicola ATCC22214. It has been reported that this yeast gives the highest yields for the production of biosurfactant sophorolipids. Hence, this yeast was used in this study. One of the objectives of this study is to increase the yield of the sophorolipid synthesis. To meet this end, basic culture medium was formulated on the basis of literature research to-date. When this medium was used, the increase in yield from 15% to 150% was observed compared to using the media in the literature. To examine how the interfacial characteristics of sophorolipids change with substrate, glucose (the first carbon source) was maintained in the media and after being cultured for three days, the second carbon sources such as alkanes, vegetable oils, alcohols or organic acids were added. The whole broth was extracted twice with ethyl acetate and the extract was analyzed by thin layer chromatograhy(TLC). After qualitative analyses by TLC, surface tensions of sophorolipids were measured by the Wilhelmy plate method and critical micelle concentration(CMC) was determined using these surface tension data. Also, interfacial tensions were measured by the spinning drop method and emulsions of the three-component water/decane/sophorolipid system were tested. Sophorolipids were effective and efficient in terms of surface tension reduction and CMC, but they were ineffective as emulsifiers because emulsions were separated within 30 minutes.

Metal-Ferroelectric-Metal(MFM) 구조의 개퍼시터에서 Pb(Zr,Ti)O3(PZT)-전극 계면층이 PZT 박막 특성에 기여하는 영향을 알아보기 위하여 Pt/PZT/계면층/Pt/TiO2/SiO2/Si 구조의 캐퍼시터를 제작하였다. 계면층으로 사용될 물질들 중에서 PbTiO3(PT) 층을 sol-gel 방법으로 형성하였으며, PbO, ZrO2, TiO2 층들을 reactive sputtering 방법으로 형성하였다. PZT박막을 구성하는 원소들로 이루어진 단순 산화물들의 특성을 평가하기 위하여 PbO, ZrO2, TiO2를 계면층으로 사용하여 600˚C에서 열처리를 실시하였고, 이 경우에는 TiO2가 가장 우수하게 PZT의 결정립 크기를 미세하게 하는 효과를 보였으나, 두께가 증가함에 따라 표면 거칠기가 증가하고 anatase 상으로 남기 때문에 강유전특성이 열화되었다. 반면에 PT 박막을 계면층으로 사용한 경우에는 결정립 크기의 감소와 더불어 전기적인 특성도 향상되었다. 또한 PZT의 핵생성 위치를 판단하기 위하여 PT 삽입층의 위치를 변화하며, 실험한 결과, 하부전극과 PZT 박막의 계면에 PT 삽입층을 형성하였을 경우에 가장 효과적인 seed로서의 역할을 하였다.

Sputter Cu(1-4.5at.%Mg) alloy를 100mTorr이하의 산소압력에서 온도를 증가시키며 열처리하였을 때 표연과 계면에서 형성된 MgO의 확산방지막 특성을 살펴보았다 먼저, Cu(Mg)/SiO2/Si 구조의 샘플을 열처리했을 때 계면에서는 2Mg+SiO2→2MgO+Si의 화학반응에 의해 MgO가 형성되는데 이 MgO충에 의해 Cu가 SiO2로 확산되는 것이 현저하게 감소하였다. TiN/Si 기판 위에서도 Cu(Mg)과 TiN 계면에 MgO가 형성되어 Cu(4.5at.%Mg)의 경우 800˚C까지 Cu와 Si의 확산을 방지할 수 있었다. 표면에 형성된 MgO위에 Si을 증착하여 Si/MgO(150 Å)/Cu(Mg)/SiO2/Si구조로 만든 후 열처리했을 때 150 Å의 MgO는 700˚C까지 Si과 Cu의 확산을 방지할 수 있었다. 표면에 형성된 MgO(150 Å)의 누설전류특성은 break down 5V, 누설전류 10-7A/cm2의 값을 나타냈다. 또한 Si3N4/MgO 이중구조에서는 매우 낮은 누설전류밀도를 나타냈으며 MgO에 의해 Si3N4 증착시 안정적인 계면이 형성됨을 확인하였다.

Sn-3.5Ag, Sn-3.5Ag-lZn Eoa납과 Cu기판과의 계면반응 및 접합특성에 관하여 검토하였다. Eoa납과 Cu기판이 접합된 시편은 100˚C와 160˚C에서 60일간 열처리하였으며, 전단하중을 가하여 강도를 측정하였다. 150˚C에서 열처리에 따른 계면반응층의 두게는 Sn-3.5Ag/Cu계면이 Sn-3.5A9-IZn/Cu계면보다 빠르게 성장하였으며, 반응생성물 성장은 t1/2에 비례하여 체적 확산 경향을 나타냈다. 계면 반응생성물은 Sn-3.5Ag/Cu계면의 경우 Cu6Sn5상이 형성되었고, Ag3Sn상은 반응층 내부 및 반응층과 땜납의 계면에 석출하였으며, Zn을 첨가한 경우에는 계면에 Cu6Sn5 상과 함께 Cu5Zn8상이 형성되었다. 땜납/기판의 전단강도는 Sn-3.5Ag합금에 Zn을 1% 첨가하면 증가하였으며, 열처리를 한 경우에는 감소하였다.

Sn-Bi-X(X:2Cu, 2Sb, 5In) 계 땜납과 Cu 기판과의 계면반응 및 기계적성질에 대하여 고찰하였다. Cu판과 땜납의 접합부는 100˚C에서 60일까지 열처리하여 광학현미경, SEM, EDS,분석을 통하여 시효처리에 따른 미세조직과 계면반응을 분석하였으며, 인장강도 및 연신율은 제조된 시편을 30일까지 열처리 한 후 0.3mm min-1로 인장하여 시험하였다. 미세조직 분석결과 Cu의 첨가로 미세조직이 미세화 됨을 알 수 있으며, 계면에 형성된 화합물은 첨가원소에 따라 다르게 나타났다. 인장시험 결과 열처리 초기에는 땜납쪽에서의 파괴가 발생하였으나 열처리 시간이 증가하면서 계면반응층고 땜납의 계면에서 파괴가 발생하였다. 열처리에 따른 인장강도는 Cu를 첨가한 경우에 가장 높은 값을 나타냈다.

In acid-catalyzed acetal cyclization of long aliphatic aldehydes(R=n-C7H15 ; n-C9H19 ; n-C11H23) with 1,1,1-tris(hydroxymethyl)propane, 2-alkyl-5-hydroxymethyl-5-ethyl-1,3-dioxanes were obtained. The final products, sodium 2-alkyl-5-(sulfonatedpropylethermethyl)-5-ethyl-1,3-propanesultion in the presence of sodium hydride. These compounds were a new group of destructible surfactants which were readily hydrolyzed and oxidized in natural water reservoirs. Physical properties of these new compounds involved some surface properties such as Krafft point(Kp), critical micelle concentration(cmc), surface tension of aqueous solutions near cmc(γmin), foaming power, emulsion power and hydrolysis properties were determined. The destructible surfactants containing 1,3-dioxane ring were synthesized to about 85±5.5% yield. The cmc values of the compounds by ring method were assumed to 0.5~5.0×10-3mol/L range and surface tensions at cmc were 29.5~33.0dyne/cm respectively at 25℃. The foaming power and foam stability were 170~230mm and 52~135mm respectively at 1×10-2mol/L, foam was occurred rarely below 1×10-3mol/L. The emulsion property of liquid paraffin was better than that of soybean oil. For hydrolysis property with ph and time, these compounds were decomposed within about 200minutes at ph1~2. Hopefully these compounds are expected to be a good O/W emulsifier that have decomposability in acid and may be used in the process which do not need foaming.

Surfactants are the surface-active molecules that display amphiphilicity, Because of this surface activity and amphiphilicity, surfactants have been used in wide industrial applications such as foods, detergents, cosmetics, medicine, polymers, paints, flotation, textiles. These days, their applications extend to high-technology industries such as microelectronics, magnetic recording material, advanced batteries, novel separations, etc. As new applications of surfactants are found and the demand of the surfactants increases, surfactant industry has been more pressed to face a formidable challenge, which is to develop surfactants that are envirionmentally friendly. In this regard biosurfactants may be alternatives to chemical surfactants, since biosurfactants are biologically compatible, more biodegradable, less toxic, and highly specific. Because of these excellent advantages over those of chemical surfactants, much efforts have been made in biosurfactant research. This article reviews biosurfactants in several aspects, that is, their definition, structures, properties, applications, and prospects.

In relation to the preparation of Langmuir-Blodgett thin film, four kinds of N-alkylpyridiniurn bromide were synthesized. The values of surface tensions of these materials, measured with a Traube stalagmometer, gave the relationship between the critical micells hydrophobic radical and between CMC and temperature. Values of thermodynamic properties(δH0m, δS0m, δG0m,) for the formatoin of micelle were also obtained. Experiments gave the following results; at the temperature range between 40 and 60℃, CMC of Hexadecyl-, Octadecyl-, Eicosyl-, and Docosyl-Pyridinium Bromide were 7.64×10-4~9.13×10-4, 3.85×10-4~4.60×10-4, 2.00×10-4~2.39×10-4, and 1.07×10-4~1.28×10-4 mol/l, respectively. Surface tension, γCMC, of those were 33.49~36.00, 34.78~37.61, 35.49~37.61 and 38.76~55.80 dyne/cm, respectively, The relationship between CMC and the mumber of carbon atoms in the hydrophobic radical, N was expressed as follows : Log(CMC)=A-BN where A and B are constants. At the temperature range between 40 and 60℃, the change of Gibbs evergy (δGm) for one methylene group (-CH2-) were -0.65RT, respectively, The minus values of enthalpy change (δHm) suggest that the formation of micelle is exothermic. Additionally, the overall increase in the entropy change (δSm) with respect to the temperature increase suggests that the formation of micelle is attained by a exothermic enthalpy directed process.

본 연구는 건조된 코아세르베이트 필름의 물리적 특성이 샴푸 건조 후 모발 사용감에 미치는 상관관계를 조사하기 위하여 실시하였다. 단순 샴푸 조성물은 동일한 조성의 계면활성제에 양이온 전하 밀도가 서로 다른 두 종류의 양이온 폴리머를 사용하여 제조하였다. 이 단순 조성물을 물에 희석하여 코아세르베이트(Coacervate)를 형성되도록 하였고,3000 rpm, 30 min 조건으로 원심 분리하여 형성된 코아세르베이트를 얻었다. 얻어진 코아세르베이트를 유리판 위에 균일한 두께로 도포하고 50 ℃ 건조기에서 1 h 건조하여 코아세르베이트 필름을 얻었다. 이렇게 얻어진 코아세르베이트 필름의 접촉각과 코아세르베이트의 SEM 이미지 조사를 수행하였고, 코아세르베이트의 수분 보유량과 수분 유지력을 동시에 조사하였다. 샴푸 후 건조된 모발의 부드러움과 보습감은 모발타래를 이용하여 전문 미용 패널이 평가를 수행하였다. 본 실험결과 건조된 코아세르베이트 필름의 특성이 샴푸 후 건조된 모발의 부드러움 및 보습감에 영향을 주는 것으로 확인되었다.