• Journal of Adhesion and Interface
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• v.17 no.2
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• pp.49-55
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• 2016

In this study, we designed an environment friendly, water-based adhesive using the acrylic emulsion method as a replacement for solvent-based adhesives, which are most commonly used in layered laminates for flexible food packaging. We designed adhesives with different combinations of anionic, non-ionic, and phosphoric ester surfactants, and with different concentrations of chain transfer agent (CTA). We also examined the effect of the degree of cross-linking by synthesizing and comparing 8 test group adhesives with different types of functional monomers. Additionally, we synthesized 2 other test group pressure-sensitive adhesives (PSA) using styrene/alpha-methyl styrene/acrylic acid (SAA) semipolymer dispersing agents (with molecular weights of 13,000 g/mol and 8,600 g/mol, respectively) to replace the conventional surfactants. We evaluated whether the 10 test group pressure-sensitive adhesives met the basic physical property criteria required for flexible food packaging by carrying out a physical analysis of their glass transition temperature (Tg), particle size, adhesion, and molecular weight. In our test, 2 test group adhesives manufactured with the combination of anionic and non-ionic surfactants, CTA concentration of 0.2%, and functional monomers of hydroxyethyl acrylate (HEA) and glycidyl methacrylate (GMA) demonstrated molecular weight and flexibility suitable for flexible packaging, with low adhesiveness and small particle size.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.334-334
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• 2006

Helical polymers like polyisocyanates with single screw sense are essential to exhibit sophisticated functions like molecular recognition, self-replication, chirality memory and catalytic activity. One approach that has not been explored is the effect on handedness of the polyisocyanates through end-capping with a chiral residue. Induction of chirality in poly(n-hexyl isocyanate) was studied by end-capping with chiral (R and S) 2-bromo-3-methylbutyryl chloride(R-BMBC and S-BMBC). We have shown that a control over living anionic polymerization of HIC by using a suitable initiator affords an opportunity to introduce chiral end-groups with 100% yield and in high purity. This has resulted in helicity induction through extended lengths several orders of magnitude.

• Macromolecular Research
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• v.17 no.12
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• pp.1010-1014
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• 2009

Monodispersed microparticles with a poly(D,L-lactide-co-glycolide) (PLGA) core and a poly(ethyl 2-cyanoacrylate) (PE2CA) shell were prepared by Shirasu porous glass (SPG) membrane emulsification to reduce the initial burst release of doxorubicin (DOX). Solution mixtures with different weight ratios of PLGA polymer and E2CA monomer were permeated under pressure through an SPG membrane with $1.9\;{\mu}m$ pore size into a continuous water phase with sodium lauryl sulfate as a surfactant. Core-shell structured microparticles were formed by the mechanism of anionic interfacial polymerization of E2CA and precipitation of both polymers. The average diameter of the resulting microparticles with various PLGA:E2CA ratios ranged from 1.42 to $2.73\;{\mu}m$. The morphology and core-shell structure of the microparticles were observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The DOX release profiles revealed that the microparticles with an equivalent PLGA:E2CA weight ratio of 1:1 exhibited the optimal condition to reduce the initial burst of DOX. The initial release rate of DOX was dependent on the PLGA:E2CA ratio, and was minimized at a 1:1 ratio.

• Macromolecular Research
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• v.11 no.3
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• pp.163-171
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• 2003

For the pervaporation of water-ethanol mixtures, new composite membranes having poly(acrylic acid)-poly (butyl methacrylate-co-methyl methacrylate) interpenetrati ng polymer network [PAA-P(BMA-co-MMA) IPN] skin layer supported on porous and crosslinked poly(BMA-co-MMA) were prepared. The morphology of the sub-layer of the composite membrane prepared in the presence of 60 wt% solvent showed cellular structure, on the other hand that of sublayer prepared in the presence of 70 wt% solvent presented very porous interconnected pore structure with macrovoids. Permeation rates of the composite membranes were largely influenced by the morphology of the sublayer. Separation factors increased with the increase of the degree of crosslinking of the PAA network. It was found that permeation rates could be increased by introducing anionic charges on carboxyl groups of the PAA. The permeation rate changes of the PAA-P(BMA-co-MMA) IPN composite membranes according to the feed compositions showed quite similar pattern with the swelling behavior in water-ethanol mixtures.

• Textile Coloration and Finishing
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• v.14 no.2
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• pp.94-94
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• 2002

A number of studies have been introduced on the use of quaternary cationic agents having various reactive groups, which can improve the substantivity of anionic dyes, specially direct dyes, towards cotton. In the case of direct dyes, it is well known that they are widely used due to their convenience to apply and low cost, whilst they display poor levels of fastness properties to washing. Thus many applications using direct dyes in the textile fields have been still enjoyed in the areas where a higher level of wet fastness is specially not required. This work herein comprises that in order to improve the substantivity of direct dyes towards cotton, cellulose-reactive allylamine polymer namely, triazinyl N,N′-dimethyl-N,N′-diallyl ammonium chloride was prepared and treated onto cotton to provide cationic properties within substrates. This application showed that even low concentration of electrolytes being present, the direct dyes were exhausted well on the cationized cotton and that the rate of dye uptake by treated cotton was faster than that of untreated sample. Furthermore the antimicrobial properties were observed from the cationized samples.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.5 no.2
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• pp.103-107
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• 2004

This paper was studied the properties of materials for treatment of anionic chromate$(CrO4^{-2})$ in industrial wastewater. Ion exchange fiber, poly(acryloamidino diethylene diamine) with ion exchange and adsorption was prepared PAN fiber and diethylenetriamine under $AlC1_3$ catalyst at $120^\circ{C}$ and was analyzed $^{{13}/C-NMR$}$ and FT-IR spectroscopy. The maximum adsorption and the coordination of chromate on chelating fiber were analyzed FT-IR spectra. We proposed the coordination structure with inter/intramolecular bond.

• Polymer(Korea)
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• v.26 no.4
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• pp.516-522
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• 2002

The ion exchange characteristic of quaternary ammonium as functional group containing aminated acrylic fibrous ion exchanger were studied for the adsorption of linear alkylbenzene sulfonate (LAS) in a continuous ion exchange process. The adsorption capacities of aminated acrylic for LAS as the adsorption temperature were increased with increasing adsorption temperature and were equilibrated at $40^{\circ}C$. The maximum adsorption capacities as column packing ratio (L/D) were obtained at L/D>2. The adsorption capacity for LAS was increased with increasing pH and the maximum adsorption capacity as pH was obtained at pH 7. The effects of temperature and pH were similar to those of flow rate and concentration of LAS tin the breakthrough curves, the breakthrough time and slope of breakthrough corves decreased with increasing flow rate and concentration of LAS in adsorption process.

• Journal of Korean Society of Water and Wastewater
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• v.24 no.5
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• pp.485-493
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• 2010

Chemical coagulation destabilizes colloidal particles so that particles grow to larger flocs. Solid particles are then removed by solid-liquid separation after typical precipitation. Rapid precipitation enhances the separation by reducing the precipitation time with larger and denser particles. Conventionally, polyelectolyte compounds (polymers) function as a flocculant aid by introducing a interparticle binding, which increases the particle size and density. And more recent ballasted flocculation adds a ballasting agent (microsand) to form denser particles with its high-density(sp gr=2.65). The current research was to evaluate the manner in which ballasted flocs are formed under different injection timings of microsand and to recognize the effects on floc formation. $FeCl_3$ as a coagulant, anionic polymer for a flocculation aid and microsand were used for the floc formation. Floc size (diameter) was widely ranged with the highest mean value when microsand was injected between $FeCl_3$ and polymer. Mean floc density was larger when the floc formed smaller. Settling velocity increased with larger floc size, whilst not significantly affected by the timing of microsand injection. The additional slow mixing on floc formation increased floc size to some extent.

• Polymer(Korea)
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• v.26 no.5
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• pp.575-581
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• 2002

Heterogeneous ion exchange membranes were prepared by mixing polyethylene as matrix with bead and fibrous anionic ion exchangers at different mixing ratio. Generally, ion exchange capacities were increased with increasing the ratio of the fibrous ion exchanger content. The highest ion exchange capacity of the membrane was 1.86 meq/g at 30wt% IXF (ion exchange fiber) in the membrane. The water uptake, fixed ion concentration, and ion transport number of the membrane increased with increasing the content of the fibrous ion exchanger. However, the electrical resistivity of the membrane was decreased with increasing the content of the fibrous ion exchanger. The lowest electrical resistivity of 5$\Omega$/$\textrm{cm}^2$ was observed at 30 wt%of IXF.

• Journal of Korean Society of Water and Wastewater
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• v.30 no.6
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• pp.663-671
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• 2016

Coagulation/precipitation process has been widely used for the removal of phosphate within domestic wastewater. Although Fe and Al are typical coagulants used for phosphate removal, these have some shortages such as color problem and low sedimentation velocity. In this study, both Fe and Al were used to overcome the shortages caused by using single one, and anionic polymer coagulant was additionally used to enhance sedimentation velocity of the precipitate formed. Batch experiments using a jar test were conducted with real wastewater, which was an effluent of the second sedimentation tank in domestic wastewater treatment plant. Response Surface Methodology was used to examine the responsibility of each parameter on phosphate removal as well as to optimize the dosage of the three coagulants. Economic analysis was also done on the basis of selling prices of the coagulants in the field. Phosphate removal efficiency of Fe(III) was 30% higher than those of Fe(II). Considering chemical price, optimum dosage for achieving residual phosphate concentration below 0.2 mg/L were determined to be 18.14 mg/L of Fe(III), 2.60 mg/L of Al, and 1.64 mg/L of polymer coagulant.