• Polymer(Korea)
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• v.26 no.5
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• pp.582-588
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• 2002

The block copolymers were prepared by the ring opening polymerizati on of DL-lactide by poly(ethylene oxide) (PEO) with diethylzinc (ZnE$_2$) as a catalyst. When the feed ratio of PEO was over 30% relative to DL-lactide, the polymerization of DL-lactide took place from the PEO hydroxyl terminals to provide the desired A -B-A or A-B block copolymer. The block copolymers were made of films by cast method and the films obtained was drawn to 2.5 times at 60 $\^{C}$. At the same draw ratio, the tensile modulus of the films was decreased with increasing PEO content in the block copolymers. It was therefore suggested that the block copolymers comprising of PDLLA and PEO, had high potentials as the biomaterials with improved flexibility.

• Textile Coloration and Finishing
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• v.10 no.5
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• pp.13-18
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• 1998

Polypropylene-ethylene/vinyl acetate copolymer (PP-EVA) blends were prepared by mechanical blending using relatively semi-crystaline ethylene-vinyl acetate copolymer and polypropylene. In order to obtain dyeable PP fiber, PP-EVA blends were prepared using below 10wt.％ of EVA and formed a filament by the melt spinning method. The resultant fibers had tensile strengh of 2∼3g/d, elongation of 330∼600%, initial modulus of 22∼46g/d, and exhibited markedly improved dyeing property.

• Bulletin of the Korean Chemical Society
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• v.24 no.1
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• pp.123-125
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• 2003

• Textile Coloration and Finishing
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• v.15 no.4
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• pp.57-64
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• 2003

Poly(ethylene-co-vinyl acetate)(EVA) microspheres were prepared by a thermally induced phase separation. The microsphere formation occurred by the nucleation and growth mechanism in the metastable region. The diluent used was toluene. The microsphere formation and growth was followed by the cloud point of the optical microscope measurement. The microsphere size distribution, which was obtained by SEM observation and particle size analyzer, became broader when the polymer concentration was higher, the content of vinyl acetate in EVA copolymer was higher, and the cooling rate of EVA copolymer solution was lower.

• Bulletin of the Korean Chemical Society
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• v.22 no.3
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• pp.261-262
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• 2001

• Polymer(Korea)
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• v.35 no.2
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• pp.146-151
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• 2011

The physical properties of poly (ethylene 2,6-naphthalate) (PEN) copolymers were studied. PEN copolymers were synthesized successfully from the mixtures of ethylene glycol(EG), 1,3-propanediol (PD) and l,4-butanediol (BD) with 2,6-dimethyl naphthalene dicarboxylate. The results indicated that PEN copolymers showed an amorphous state when the content of BD(PD) in applied EG/BD(EG/PD) mixtures was less than 40% during the polycondensation. As a result, the lowering of thermal properties, orientation, and mechanical properties was found, however, the dimensional stability was improved. This is a promising result to apply the synthesized PEN copolymers as flexibles substrates.

• Polymer(Korea)
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• v.36 no.1
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• pp.104-110
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• 2012

The dispersion of pigment particles is important because it is capable of increasing the color strength, contrast, and transmittance of color-LCD products. Pigment dispersion properties are very important factors for the quality of LCD color filters. The chemical structure of polymeric dispersants for pigment is important to improve dispersion stability and prevent aggregation or flocculation of pigment in organic or aqueous systems. Polymeric dispersants should contain both anchoring group that interacts with pigment surface and stabilizing group that provides steric stabilization. Moreover, the molecular weight and composition of block copolymer have the an effect on pigment dispersion. In this study, adequate dispersants, block copolymers containing (2-dimethylamino)ethyl methacrylate as anchoring group and oligo(ethylene oxide)methyl ether methacrylate as a stabilizing group were designed and synthesized by atom transfer radical polymerization in order to prepare well-defined structure, molecular weight and composition.

• Bulletin of the Korean Chemical Society
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• v.28 no.5
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• pp.795-799
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• 2007

The bulk properties of poly(γ-benzyl-L-glutamate)-poly(ethylene glycol), PBLG-PEO, diblock copolymer were investigated. The helical transition from 7/2 to 13/5 for pure PBLG was at 120 oC while those of GE-1 and GE-2, which contain flexible PEO block 40 wt% and 60 wt% respectively, were shown at 135℃ on DSC experiments. FT-IR and XRD experiments were shown that the diblock copolymers maintained their α-helical structure in the temperature range between 25℃ and 175℃. Increasing relative size of coil part resulted in the increase of intermolecular packing distances. Due to well-maintained helical structure, lyotropic LC phases were observed for the PBLG-PEO block copolymer by the polarized optical microscope (POM). Especially, GE-3 copolymer, which has 12.5 wt% PEO contents, showed the smectic C phase. The competition of favorable aggregation energy between rod-rod and coil-coil, and unfavorable aggregation energy of rod-coil give rise to change the supramolecular structure in mixed solvent.

• Macromolecular Research
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• v.16 no.3
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• pp.231-237
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• 2008

Biodegradable poly($\varepsilon$-caprolactone-co-L-lactide)-b-poly(ethylene glycol) (PCLA-b-PEG) copolymers were synthesized via solution polymerization by varying the feed composition of $\varepsilon$-caprolactone ($\varepsilon$-CL) and L-lactide (LLA) ($\varepsilon$-CL: LLA= 10:0, 7:3, 5:5, 3:7, 0: 10). The feed ratio based on weight is in accordance with the copolymer composition except for the case of $\varepsilon$-CL: LLA=3:7 (C3L7), which was verified by $^1H$-NMR. Two different approaches were used for the exceptional case, which is an extension of the reaction time or the sequential introduction of the monomer. A copolymer composition of $\varepsilon$-CL: LLA=3:7 could be obtained in either case. The chemical microstructure of PCLA-b-PEG was determined using the $^{13}C$-NMR spectra and the effect of the sequential structure on the thermal properties and crystallinity were examined. Despite the same composition ratio of the copolymer, the microstructure can differ according to the reaction conditions.

• Polymer(Korea)
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• v.29 no.2
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• pp.127-134
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• 2005

The relationships among mechanical properties, rheological properties, and morphology by reactive extrusion based on commingled pckaging film wastes contains polypropylene (PP) pckaging film system [PP/polyethylene (PE)/aluminum (Al)/poly(ethylene terephthalate) (PET)] and Nylon packaging film system[Nylon/PE/linear-low density polyethylene (LLDPE)] were investigated to improve the compatibility and toughness of these wastes using various compatibilizers such as ethylene vinylacetate (EVA), styrene-ethylene/butylene-styrene triblock copolymer (SEBS), styrene-ethylene/butylene-styrene-graft-maleic anhydride copolymer (SEBS-g-MA), polyethylene-graft-maleic anhydride (PE-g-MA), polypropylene-graft-maleic anhydride (PP-g-MA) , polyethylene-graft-acrylic acid (PE-g-AA) and polypropylene-graft-acrylic acid (PP-g-AA). Compared with simple melt blend system, the blends showed improvement of about $50\%$ increase in physical properties when SEBS and EVA were added. However, SEBS-g-MA thermoplastic elastomer which is highly reactive with amine terminal group of nylon, resulted in about $200\%$ increase in impact strength. This compatibilization effect resulted from the increase of interfacial adhesion and the reduction of domain size of dispersed phase in PP/Nylon blend system.