• Membrane Journal
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• v.19 no.2
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• pp.122-128
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• 2009

We prepared monodispersed spherical silica microgels by controlling various conditions of emulsification procedure using a lab-scale membrane emulsification system equipped with SPG (Shirasu porous glass) porous membrane having pore size of $1.5{\mu}m$. We determined the effects of process parameters of membrane emulsification (ratio of dispersed phase to continuous phase, sodium silicate concentration, emulsifier concentration, dispersed phase pressure, stirring speed) on the mean size and size distribution of silica microgels. The increase of the ratio of dispersed phase to continuous phase, dispersed phase pressure and sodium silicate concentration led to the increase in the mean size of microgels. On the contrary, the increase in emulsifier concentration and stirring speed of the continuous phase caused the reduction of the mean size of microgels. Through controlling these parameters, monodisperse spherical silica microgels with about $6{\mu}m$ of the mean size were finally prepared.

• Journal of Energy Engineering
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• v.10 no.2
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• pp.83-89
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• 2001

This paper studies the possibility of applying the EIT(Electrical Impedance Tomography) technique for investigating the formation and movement of dispersed phase droplets as they stream through a Direct Contact Heat Exchanger(DCHX). In most direct contact liquid-liquid heat exchangers, oil or hydro-carbon with a density different (lighter or heavier) from water is normally used as dispersed working fluid. The main difficulty that arises with arrangement lies in the extraction of performance parameters and visualization of dispersed phase fluids if required. In order to delve into these problems, this paper introduces a number of cases regarding the operation and principle of DCHXs and investigates the possibility of applying the EIT technique whose results are given for several examples.

• Korea-Australia Rheology Journal
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• v.11 no.3
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• pp.241-246
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• 1999

In this study, we consider the effect of nonionic surfactants on the rheological responses of emulsion systems under the action of a uniform do electric field. The model emulsions consist of a less conducting dispersed phase and a more conducting continuous phase. When the shear flow is weak, the positive viscosity effect is produced due to the formation of chain-like morphology. The nonionic surfactants used here generate two distinctively different effects. Specifically, first, the steric hindrance induced by the surfactant molecules renders the structure unstable, and thereby reduces the degree of positive viscosity effect. Secondly, the presence of surfactant molecules also prevents the rotation of the dispersed droplets by anchoring across the interface or by decreasing the size of dispersed phase. The second effect suppresses the negative viscosity effect.

• Fibers and Polymers
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• v.5 no.2
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• pp.145-150
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• 2004

Blends of poly(phenylene sulfide) (PPS) and polyethylene, either linear low density polyethylene (LLDPE) or metallocene-catalyzed polyethylene (MPE), that were prepared by melt blending, were investigated. From the rheological properties as determined by capillary rheometry, the melt viscosity of both PPS/LLDPE and PPS/MPE blends was low when PE was in dispersed phase, but high melt viscosity was observed for both blends with PPS in dispersed phase. Significant differences depending on the composition were found in the mechanical properties such as percent elongation at break and notched Izod impact strength. In addition, dispersed phase morphology of the blends was analyzed by a scanning electron microscope (SEM), together with brief discussion about the difference between them.

• Korea-Australia Rheology Journal
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• v.11 no.4
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• pp.269-273
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• 1999

Immiscible polymer blends containing a liquid crystalline polymer dispersed phase can be described by existing blend theories when the dispersed-phase droplets are large relative to the orientation correlation length ("domain size") of the LCP. There does not appear to be an interfacial contribution to the linear viscoelastic properties of the blend from droplets smaller than the correlation length. Polyester blends, where interfacial interactions occur between the LCP and the matrix, exhibit a reduction in viscosity to below the viscosity of either component at low shear rates, where the droplet morphology is spherical. These anomalies cannot be explained in the context of existing theory.ng theory.

• Korean Chemical Engineering Research
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• v.53 no.6
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• pp.709-716
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• 2015

In this study, structural developments of polypropylene / ionomer / clay ternary composites were investigated depending on the dispersion and localization of clay. The changes in physical properties were observed adding organoclays 1~10wt% to 90% polypropylene and 10% ionomer blends. The organoclays were localized inside of the dispersed phase under the composition of 3wt%, however, over that composition, clay particles formed stiff network structure in the dispersed phase and additional clays were localized at the interface between two phases. According to the developments of microstructure, the interaction of ternary composites changed from polypropylene-ionomer to polypropylene-ionomer and ionomer-clay which affected rheological properties. The storage modulus (G') of the composites was similar to the blends when clays were localized inside of dispersed phase but increased when clays were localized at interface. Also, the fractured morphology of the composites showed phase boundary and growing radius of dispersed phase depending on addition of fillers when clays were found inside. However, when fillers found at the interface between blends, the radius of the dispersed phase decreased and compatibilized morphology were observed. The interfacial interaction of the ternary composite was quantified depending on the structural development of dispersed phase and localization of clay particles by the rheological properties. The interaction of composites at solid state which was measured through peel adhesion strength increased by growth of interfacial interaction of each component. Furthermore, the crystallinity of the composites was decreased when the clay particles were localized at the interface.

• Macromolecular Research
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• v.17 no.12
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• pp.943-949
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• 2009

A highly dispersed W/O emulsion of silicone oil (cyclomethicone)/water system was prepared with a nonionic surfactant. The surface and interfacial tension between the oil and water were characterized in terms of the droplet size distribution and viscosity change of the emulsion. When the dispersed phase concentration was relatively high, the viscosity of the emulsion was rapidly increased and the droplet size of the emulsion was decreased. The rheological behavior of the emulsion system showed non-Newtonian and shear thinning phenomena depending upon the content of the dispersed phase. The droplet size of the emulsion was decreased with increasing surfactant content and water concentration. The relative viscosity of the emulsion was better predicted with the Choi-Schowalter model than with the Taylor model. The value of the complex modulus increased with increasing surfactant concentration. The linear viscoelastic region was expanded with a dispersed phase concentration. According to the change in the viscosity, the behavior was classified into three distinct regions: [I] linear viscoelastic, [II] partially viscoelastic, and [III] viscous. The creep/recovery behaviors in each region were characterized.

• Transactions of the Korean Society of Mechanical Engineers
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• v.18 no.12
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• pp.3276-3286
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• 1994

In most direct contact liquid-liquid heat exchangers, oil or hydrocarbon with a density less than water is normally used as dispersed working fluid. The main difficulty that arises with this arrangement lies in the control of the interface at the top of the column. When it is connected with a solar collector which uses water as its working fluid, the main difficulties arise from the fact that the water can be frozen during winter time. In order to solve these problems and to demonstrate the technical feasibility of a direct contact liquid-liquid heat exchanger, liquids heavier than water with low freezing temperature has been utilized as dispersed phase liquids in a small laboratory scale model made of pyrex glass. In the present investigation, dimethyl phthalate(C/sub 6/H/sub 4/)COOCH/sub 3/)/sub 2/) and diethyl phthalate (C/sub 6/H/sub 4/(CO/sub 2/C/sub 2/H/sub 5/)/sub 2/) are utilized as heavy dispersed phase working fluids. The results of the present investigation the technical in the utilization of heavier dispersed working liquid in the spray-column liquid-liquid heat exchanger for a solar system. The overall average temperature difference along the column is found to be almost half of the initial temperature difference between the dispersed and the continuous phase. Despite the fact that the two phthalates tested in the experiment differ significantly in some of their physical properties, the volumetric heat transfer coefficients in terms of dispersed fluid superficial velocities were found to be similar for both phthalates tested.

• Transactions of the Korean Society of Mechanical Engineers B
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• v.24 no.6
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• pp.886-893
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• 2000

The Characteristics of dividing the dispersed bubble, plug, and slug steam-water flow in the horizontal junctions with horizontal branches have been experimentally investigated. The experimental investigation of the separation phenomena in a $45^{\circ}$ horizontal wye with equal pipe inner diameter of 25 mm is presented to provide a data base for the development and verification of the analytical models. The phase separation and pressure distribution in the three legs of each test section are obtained through the set of measurements made in the present work. And the dependence of phase separation on different parameters, such as inlet quality and mass flux, is discussed.

• Applied Chemistry for Engineering
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• v.10 no.2
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• pp.231-236
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• 1999

Several series of morphologically controlled $MoO_3$/$SiO_2$ catalysts were prepared, characterized, and tested for hydrodesulfurization (HDS) of dibenzothiophene (DBT) activity. Molybdenum surface loaded with 4.0 atoms $Mo/nm^2$ was prepared as sintered hexagonal and sintered orthorhombic, as well as a novel "well dispersed hexagonal" phase. Characterization by XRD, Raman, and $O_2$ chemisorption results reveals that the dispersion of $MoO_3$ over silica depends on the final $MoO_3$ phase in the order of; sintered hexagonal < sintered orthorhombic < dispersed hexagonal phase. Temperature programmed reduction (TPR) results show that both bulk and dispersed microcrystalline of $MoO_3$ reduce to $MoO_2$ at $650^{\circ}C$ and to Mo metal at $1000^{\circ}C$. HDS of DBT was performed in a differential reactor at 30 atm over the temperature range $350{\sim}500^{\circ}C$. Activity of $MoO_3$/$SiO_2$ toward HDS of DBT is proportional to dispersion.