• Macromolecular Research
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• v.13 no.2
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• pp.102-106
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• 2005

Poly(methyl methacrylate) (PMMA)/sodium montmorillonite (Na-MMT) nanocomposites were prepared with a novel method utilizing a macroazoinitiator (MAI). To induce the intergallery polymerization of methyl methacrylate (MMA), the MAI containing a po1y(ethylene glycol) (PEG) segment was intercalated between the lamellae of Na-MMT and swelled with water to enhance the diffusion of MMA into the gallery. The structure of the nanocomposite was examined using X-ray diffraction and transmission electron microscopy, and the thermal properties were examined using differential scanning calorimetry and thermogravimetry. The PMMA/Na-MMT nanocomposite prepared by intergallery polymerization showed a distinct enhancement of its thermal properties; an approximately $30^{\circ}C$ increase in its glass transition temperature and an $80\sim100^{\circ}C$ increase in its thermal decomposition temperature for a $10\%$ weight loss.

• Polymer(Korea)
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• v.29 no.4
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• pp.380-384
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• 2005

Fluoroalkyl methacrylate and acrylic acid were bulk radical copolymerized in the presence of pure sodium montmorillonite or macromer intercalated sodium montmorilonite to get a fluorinated acrylic ionomer/sodium montmorillonite composite, and their physical properties, such as X-ray diffraction pattern, tensile properties, and water uptake, were examined. These composites were used to preparean ionic acrylic polymer-platinum composite (IPMC). The current and deformation responses of these IPMCs by external voltage applied across the platinum electrodes deposited on both sides of IPMC showed that the cation migration from anode to cathode was suppressed in the presence of sodium montmorillonite, causing reduced current and deformation.

• Applied Chemistry for Engineering
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• v.10 no.8
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• pp.1216-1220
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• 1999

Different amounts of zinc stearate were incorporated as a plasticizer into poly(styrene-co-sodium methacrylate) ionomers prepared by bulk-suspension plymerization and neutralization with sodium hydroxide and effects of the zinc stearate on the thermal and rheological properties were investigated. It was obseved that the crystallization of zinc stearate in the ionomers were partially suppressed depending on the content of ionic moieties. It is postulated that the ionic moieties dissolved zinc stearate and suppressed crystallization of the zinc stearates. We speculated that 0.4~0.6 mole of zinc stearate was dissolved by one mole of the ionic moiety. Poly(styrene-co-sodium methacrylate) containing only the dissolved zinc stearates showed typical rheological properties of homogeneous systems in Cox-Mertz plots. However, poly(styrene-co-sodium methacrylate) containing crystallizable zinc stearates as well as dissolved ones showed typical rheological properties of heterogeneous systems.

• Journal of the Korean Applied Science and Technology
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• v.20 no.4
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• pp.353-357
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• 2003

Sodium azide (SA) is commonly used as propellant for inflating automatic safety bags and other chemical manufacturing purposes. The investigation of potentially thermal hazard of sodium azide and its mixture with polymers are very important because it can occur an expected traffic accident so we took a experiment s using different scanning calorimeter (DSC) in nitrogen atmosphere. The decomposition temperature were about $350{\sim}450^{\circ}C$. We could find not only exothermic reaction was remarkably decreased in mixture s of acrylonitrile-butadiene-styrene (ABS) and polyvinyl chloride (PVC), but also increasing mixed rate of ABS, polyvinyl alcohol (PVA) and polymethyl methacrylate (PMMA) decreased thermal decomposition heat.

• Journal of the Korean Applied Science and Technology
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• v.25 no.1
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• pp.83-90
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• 2008

The core-shell latex particles were prepared by sequential emulsion polymerization using alkyl methacrylate as a shell monomer and potassium persulfate (KPS) as an initiator. We study the effects of core-shell structure of calcium carbonate/alkyl methacrlyate in the presence of an anionic surfactant sodium lauryl sulfate (SLS) and polyoxyethylene alkyl ether sulfate (EU-S133D)). The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of latex by transmission electron microscope (TEM).

• Journal of Adhesion and Interface
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• v.14 no.1
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• pp.1-12
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• 2013

Multi core-shell composite particles were prepared by the water-born emulsion polymerization of various core monomers such as methyl methacrylate (MMA), ethyl methacrylate (EMA) and shell monomers such as MMA, EMA, 2-hydroxyl ethyl methacrylate (2-HEMA), glycidyl methacrylate (GMA) and methacrylic acid (MAA) in the presence of different concentrations of sodium dodecyl benzene sulfonate (SDBS). The following conclusions are drawn from the conversion, particle size and distribution, average molecular weight, molecular structure, glass transition temperature with DSC, contact angle after plasma treatment, tensile strength and isothermal decomposition kinetics. In the case of the concentration of 0.02 wt% SDBS, the conversion of MMA core-(EMA/GMA) shell composite particles was excellent as 98.5%. In the case of the concentration of 0.03 wt% SDBS, the particle size of EMA core-(MMA/GMA) shell composite particles was high as $0.48{\mu}m$. We confirmed that 3 points of glass transition temperatures appear for multi core-shell composite particles compared to 1~2 points of glass transition temperatures appear for general copolymer particles. Overall, the adhesion strength of shell composite particles was in the order of EMA/MAA > EMA/2-HEMA > EMA/GMA.

• Journal of Biomedical Engineering Research
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• v.8 no.2
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• pp.123-134
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• 1987

The transport phenomena of alkali metal chlorides through poly(2 hydroxyethyl methacrylate) hydrogel membrane have been studied using electrodialysis. The hydrogel membranes were prepared by the polymerization of 2-hydroxvethyl methacrylate in the presence of 45%(V/V) H2O and ethyleneglycodimethacrylate. The initiator used in the polymerization was azobismethylisobutyrate (AMIB) prepared from azobisiobtyronitrile (AIBN) using Mortimer method. The permeability of alkali metal chlorides such LiCl, NaCl and KCI at 50 voltage was obtained. The permeability of NaCl was also observed at 30, 40, 50, and 60 voltages respectively. The concentration of solutes permeated through the membrane was measurer by flame photometry. The experimental results have been discussed with the comparison of apparent solute molecular size, the self-diffusion coefficient of solutes, the transport number of cations in aqueous solution. These indic aloes that poly(2 hydroxyethyl methacrylate) hydrogel membrane shows a specific selectivity for sodium ion.

• Polymer(Korea)
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• v.26 no.5
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• pp.653-660
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• 2002

The volume phase transition of poly(N-isopropylacrylamide) (PNIPAAm) and poly (N-isopropylacrylamide-co-sodium methacrylate) (P (NIPAAm-co-SMA)) hydrogels crosslinked with poly (ethylene glycol) diacrylate (PEGDA) was investigated in consideration of water content and surface area. The volume phase transition temperature of hydrogel was not affected by the concentration of crosslinking agent, which increased over 40$\^{C}$ by incorporating a small amount of SMA. Higher volume phase transition temperature was obtained when PEGAD was used as a crosslinking agent, suggesting that the chain length of crosslinking agent had a significant effect on the volume phase transition temperature. The surface area of PNIPAAm and P (NIPAAm-co-SMA) gels fell off around the volume phase transition temperature, resulting from the fact that the size of pores reduced remarkably in the course of the volume phase transition. Hence, the surface area and the pore size were considered to be important factors indicating the volume phase transition.

• Polymer(Korea)
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• v.28 no.1
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• pp.86-91
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• 2004

Hydrogels with enhanced biocompatibility and biostability were prepared by copolymerization of 2-hydroxyethyl methacrylate (HEMA) and sodium methacrylate (SMA) at high monomer concentration to replace a sponge which has limited applications as an implant material. It was found that incorporation of SMA moiety suppressed cytotoxicity. P(HEMA-co-SMA) hydrogel prepared at SMA feed ratio of 0.05 showed minimal cytotoxicity as compared with a normal cell culture plate. The adhesion and the spreading of cells were preferred on the surface of the hydrogel prepared with SMA feed ratio of 0.01. On the other hand, the hydrogel prepared with SMA feed ratio of 0.05 showed lower cell adhesion. Histological findings revealed no evidence of significant foreign body reaction in the tissues around the copolymer hydrogels. Conclusively, it is suggested that the hydrogels prepared by copolymerization of HEMA and SMA at high monomer concentration are strong candidates for an implant material with excellent biocompatibility and biostability.

• Journal of the Korean Applied Science and Technology
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• v.22 no.2
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• pp.96-105
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• 2005

Core-shell polymers of methyl methacrylate-styrene system were prepared by sequential emulsion polymerization in the presence of sodium dodecyl benzene sulfonate(SDBS) as an emulsifier using ammonium persulfate(APS) in an initiator and the characteristics of these core-shell polymers were evaluated. Core-shell composite latex has the both properties of core and shell components in a particle, whereas polymer blends or copolymers show a combined physical properties of two homopolymers. This unique behavior of core-shell composite latex can be used in various industrial fields. However, in preparation of core-shell composite latex, several unexpected matters are observed, for examples, particle coagulation, low degree of polymerization, and formation of new particles during shell polymerization. To solve this matters, we study the effects of surfactant concentrations, initiator concentrations, and reaction temperature on the core-shell structure of PMMA-PSt and PSt-PMMA. Particle size and particles distribution were measured by using particle size analyzer, and the morphology of the core-shell composite latex was observed by using transmission electron microscope. Glass temperature was also measured by using differential scanning calorimeter. To identify the core-shell structure, pH of the composite latex solutions was measured.