• 대한화장품학회지
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• 제23권2호
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• pp.71-96
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• 1997

We have used a novel liquid surface forces apparatus to determine the variation of disjoining pressure with film thickness for dodecane-water-dodecane emulsion films. The LSFA allows measurement of film thicknesses in the range 5-100 nm and disjoining pressure from 0-1500 Pa. Disjoining pressure isotherms are given for films stabilised by the nonionic surfactnat n-dodecyl pentaoxyethylene glycol ether$(C_{12}E_5)$ and n-decyl-$\beta$-D-glucopyranoside($C_{10}- $\beta$-Glu)$ and the anionic surfactant sodium bis(2-ethylhexyl) sulphosuccinate(AOT) in the presense of added electrolyte. For $C_{12}E_5$ and AOT, the emulsion films are indefinitely stable even for the highest concentration of NaCl tested (136.7 Nm) whereas the $C_{10}-{eta}-Glu$ film shows coalescence at this salt concentration. For film thicknesses greater than approximately 20 nm with all three surfactants, the disjoining pressure isotherms are reasonably well described in terms of electrostatic and van der Waals, forces. For the nonionic surfactant emulsion films, the charge properties of the monolayers are qualitatively similar to those seen for foam films. For AOT emulsion films, the monolayer surface potentials estimated by fitting the isotherms are similar to the values of the zeta potential measured for AOT stabilised emulsion droplets. For thin emulsion films certain systems showed isotherms which suggested the presence of an additional repulsive force with a range of approximately 20 nm.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2007년도 춘계학술대회B
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• pp.1912-1915
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• 2007

The disjoining pressure is critical in modeling the transport phenomena in small scales. They are very useful in characterizing the non-continuum effects that are not negligible in heat and mass transports in the film of less than submicro-scales. We present he disjoining pressure of thin film absorbed on solid substrate using Molecular Dynamics Simulation (MD). The disjoining pressure with respect to the film thickness is accurately calculated in the resolution of a molecular scale. The characteristics of the pressure are discussed regarding the molecular nature of the fluid system like molecular diameter and intermolecular interaction. Also, the MD results are compared with those based on the macroscopic approximation of the slab-like density profile. Significant discrepancy is observed when the effective film thickness is less than several molecular diameter

• 대한기계학회논문집B
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• 제33권2호
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• pp.101-106
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• 2009

The disjoining pressure is an important physical property in modeling the small-scale transport phenomena on thin film. It is a very useful definition in characterizing the non-continuum effects that are not negligible in heat and mass transport of the film thinner than submicro-scales. We present the calculated values of disjoining pressure of He, Kr and Xe thin films absorbed on graphite substrate using Molecular Dynamics Simulation (MD). The disjoining pressure is accurately calculated in the resolution of a molecular scale of the film thickness. The characteristics of the pressure are discussed regarding the molecular nature of the fluid system such as molecular diameter and intermolecular interaction parameters. The MD results are also compared with those based on the continuum approximation of the slab-like density profile and the results on other novel gases in the previous study. The discrepancies of the continuum model with MD results are shown in all three configurations and discussed in the view point of molecular features.

• 콘크리트학회논문집
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• 제18권2호
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• pp.213-218
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• 2006

시멘트페이스트 공극 내 확장 메니스커스 영역을 초승달 영역, 박막 영역, 흡착 영역으로 구분하고 공극 크기에 따른 액막 두께, 흡착층 두께, 모세관 압력, 분리 압력을 압력 평형 방정식을 이용하여 산정하였다. 그 결과 공극 크기와 흡착층 두께와의 연관식을 도출할 수 있었으며, 공극 크기 $1nm{\sim}1{\mu}m$에 따른 흡착층 두께는 $0.299{\sim}2.700nm$로 나타났고 특히 10nm이하의 공극에서 흡착층 두께 감소에 따른 분리압력의 증가효과가 크게 나타났다. 따라서 시멘트페이스트의 자기 수축은 10nm이하의 공극이 생성되면서 크게 증가하는 것으로 판단된다. 이러한 분리 압력과 모세관 압력을 수축 구동력으로 적용한 자기 수축 예측치는 실험값에 비하여 재령 $1{\sim}4$일까지는 작게 이후부터는 큰 결과를 나타내었다. 이는 초기재령에서의 공극측정시 공극 손상과 이에 따른 수축구동력 과소평가와 불포화 개별공극 가정에 따른 수축구동력 과대평가의 상호작용으로 판단되므로 추후 이에 대한 보완점으로 수화도등의 공극 대체 모델과 불포화공극에 대한 고려사항이 필요할 것으로 판단된다.

• 대한기계학회논문집B
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• 제27권1호
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• pp.17-24
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• 2003

A mathematical model of the hydrodynamic and heat transfer performances of two-phase flow (gas-liquid) in thin film region of micro channel is proposed. For the formulation of modeling, the flow of the vapor phase and the shear stress at the liquid-vapor interface are considered. In this work, disjoining pressure and capillary force which drive the liquid flow at the liquid-vapor interface in thin film region are adopted also. Using the model, the effects of the variations of channel height and heat flux on the flow and heat transfer characteristics are investigated. Results show that the influence of variation of vapor pressure on the liquid film flow is not negligible. The heat flux in thin-film region is the most important operation factor of micro cooler system.

• Korean Chemical Engineering Research
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• 제51권4호
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• pp.527-530
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• 2013

이 논문은 콜로이드 입자가 기름-물 사이의 계면으로 흡착될 때 필수적으로 존재하는 정전기적 반발력에 대한 실험적, 이론적 연구이다. 광집게(optical laser tweezers)와 피에조(piezo controller)를 사용하여, 개별 입자를 트랩(trap)한 후, 계면으로 강제 전이시킨다. 이때 수용액이 전해질을 포함한 경우에만, 입자가 계면으로 전이되며, 포함하지 않을 경우에는 흡착이 일어나지 않는다. 이러한 현상을 근본적으로 이해하기 위해, 광학 트랩핑 힘(optical trapping force)과 입자와 계면 사이에 존재하는 정전기적 분리압력(electrostatic disjoining pressure)를 정량적으로 계산하였다. 이를 바탕으로, 입자가 계면으로 흡착될 때, 그들 사이에는 필연적으로 문턱 에너지(threshold energy)가 존재함을 밝혀냈다. 콜로이드 입자가 에멀젼(emulsions)이나 거품(foams)등 두 개 이상의 섞이지 않는 유체계면을 안정화 시키는 "콜로이드 계면 활성제(colloid surfactants)" 역할을 한다는 사실을 고려했을 때, 본 연구는 이러한 입자의 흡착 현상을 근본적으로 이해하는데 있어서 중요한 지식을 제공한다.

• Interaction and multiscale mechanics
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• 제3권2호
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• pp.157-171
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• 2010

In this paper, a theoretical method has been developed for the electric double layer interaction under condition of the variable dielectric permittivity of water. Using Poisson-Boltzmann equation (PBE), for one plate and two plates having similar or dissimilar constant charge or constant potential, we have investigated the electric double layer potential, its gradient and the disjoining pressure as well as the effect of variation of dielectric permittivity on these parameters. It has been assumed that plates are separated by a specific distance and contain a liquid solution in between. It is shown that reduction of the dielectric permittivity near the interfaces results in compression of electric double layers and affects the potential and its gradient which leads to a decreased electrostatic repulsion. In addition, it is shown that variation of dielectric permittivity in the case of higher electrolyte concentration, leads to a greater change in potential distribution between two plates.

• 한국자기학회지
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• 제5권5호
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• pp.645-649
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• 1995

The depletion of thin liquid films due to the combined effect of centrifugation, surface roughness, and air-shear has recently been studied. While surface roughness of a rotating solid disk can be represented by deterministic cures, it has been argued that spatial random processes provide a more realistic description. Chiefly because of surface roughness, there is an asymptotic limit of retention of a thin film flowing on the rotating disk. The aim of this article is to model the depletion of thin-film flow and analyze the interplay of centrifugation, surface tension, viscosity, air-shear, disjoining pressure, and surface roughness that affect the depletion of the film. Also, the robustness of stochastic description of surface roughness is examined.

• International Journal of Concrete Structures and Materials
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• 제10권1호
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• pp.113-124
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• 2016

This paper presents the effect of silica fume and nano silica, used individually and in combination with the set accelerator and/or hydrated lime, on the properties of class F high volume ultra fine fly ash (HV-UFFA) cement composites, replacing 80 % of cement (OPC). Compressive strength test along with thermogravimetric analysis, X-ray diffraction and scanning electron microscopy were undertaken to study the effect of various elements on the physico-chemical behaviour of the blended composites. The results show that silica fume when used in combination with the set accelerator and hydrated lime in HV-UFFA cement mortar, improves its 7 and 28 day strength by 273 and 413 %, respectively, compared to the binary blended cement fly ash mortar. On the contrary, when nano silica is used in combination with set accelerator and hydrated lime in HV-UFFA cement mortar, the disjoining pressure in conjunction with the self-desiccation effect induces high early age micro cracking, resulting in hindering the development of compressive strength. However, when nano silica is used without the additives, it improves the 7 and 28 day strengths of HV-UFFA cement mortar by 918 and 567 %, respectively and the compressive strengths are comparable to that of OPC.