• Journal of the Korean Applied Science and Technology
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• v.26 no.1
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• pp.93-101
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• 2009

Antistatic acrylic resin is made from n-butyl methacrylate, methyl methacrylate, dimethyl amino ethyl methacrylate(DMAEMA), 2-ethyl hexyl methacrylate, hydroxy ethyl methacrylate, 2,2'-azobis iso-butyronitrile by synthesis. To achieve a lowest surface resistance of antistatic acrylic resin was applied to a variety of synthesis processes. The acrylic resin has been determined from the value of surface resistance and -then the antistatic acrylic resin including dimethyl amino ethyl methacrylate of the 10%, 20% and 30% is synthesized. Finally, dimethyl sulfate(DMS) on a variety of weight ratios is added to antistatic acrylic resin. When DMAEMA / DMS weight ratio is 1/1, antistatic acrylic resin isn't haze the lower the surface resistance. Compared to the traditional antistatic agent, all aspects of the physical properties is outstanding.

• Polymer(Korea)
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• v.24 no.6
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• pp.854-859
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• 2000

The synthesis of poly(N,N-dimethylamino ethyl methacrylate (DMAEMA)-block-poly(ethylene glycol) (PEG)) copolymer has been carried out and the block copolymer was characterized by FT-IR, DSC, and $^1$H-NMR. The formation of polymeric nanoaggregation was observed in the solution mixture of poly(DMAEMA) -block-PEG copolymer and poly (ethyl acrylamide) (EAAm) due to the intermolecular interaction via hydrogen bond between DMAEMA and poly(EAAm). The formation of polymeric nanoaggregation was observed above critical micelle concentration (CMC).

• Proceedings of the KAIS Fall Conference
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• 2000.10a
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• pp.245-250
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• 2000

고습도 또는 결로시 내수성을 지니는 저항형 습도센서를 제조하기 위하여 vinylbenzyl tributyl phosphonium chloride를 포함하는 4원 공중합체를 합성하여 저습도와 고습도 범위에서 측정이 가능한 습도센서용 감습막을 제작하였다. 1,5-dibrompentane과 4차 염화 가교 반응을 통하여 최종 저항형 습도센서를 제작하였다. 감습막은 알루미나 기판에 한 쌍의 금 paste가 인쇄된 전극을 사용하였으며, 감습막은 다양한 비율의 vinylbenzyl tributyl phosphonium chloride, 2-(dimethlamino)ethyl methacrylate, 2-ethylhexyl acrylate, 그리고 [2-(methacryloyloxy)ethyl]trimethyl ammonium chloride 등을 이용하여 제조하였다. 감습막은 micro-syringe를 이용하여 도포하였으며 건조 oven에서 50℃에서 6시간 동안 가교반응을 진행하였다. 습도센서의 임피던스 특성은 2-(dimethylamino)ethyl methacrylate 또는 [2-(methacryloyloxy)ethyl]trimethyl ammonium chloride의 함량이 증가할수록 감소하였다. vinylbenzyl tributyl phosphonium chloride / 2-(dimethylamino)ethyl methacrylate / 2-ethylhexyl acrylate / [2-(methacryloyloxy)ethyl]trimethyl ammonium chloride의 조성비가 4/4/1/1인 공중합체의 경우 30-90%RH 범위에서 2.64 ㏁ - 3.11 ㏀의 임피던스 특성을 보였으며 우수한 직선성과 낮은 히스테리시스 나타내었다.

• Polymer(Korea)
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• v.33 no.3
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• pp.230-236
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• 2009

Water soluble vinyl acetate/alkyl methacrylate copolymers were prepared by the emulsion copolymerization of vinyl acetate and various methacrylates such as methyl methacrylate (MMA) and ethyl methacrylate (EMA). Potassium persulfate (KPS) and ammonium persulfate (APS) were used as an initiator. Poly (vinyl alcohol) (PVA) was used as a protective colloid. The drying characteristics of the prepared poly(vinyl acetate-co-methyl methacrylate) (PVAc/PMMA), poly(vinyl acetate-co-ethyl methacrylate) (PVAc/PEMA) were studied using moisture meter at the temperature between 100 and $200^{\circ}C$. The significant results are described as follows. The activation energy of the isothermal drying process of the copolymers has the order of PVAc/PMMA> PVAc/PEMA> PVAc.

• Journal of Adhesion and Interface
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• v.11 no.2
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• pp.63-69
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• 2010

In this study, acryl resin PSA containing hydroxyl group based on 2-EHA (2-ethyl hexyl acrylate), 2-EHMA (2-ethyl hexyl methacrylate), 2-HEA (2-Hydroxy ethyl acrylate), acrylic acid was synthesized and then, isocyanate modified acryl resin PSA prepared with adduct reaction according to the amount of MOI (Methacryloyloxyethyl isocyanate) or 2-isocyanatoethyl methacrylate that can improve the curing property. This research shows that the initial PSA and peel adhesion are decreased according to the increase of the amount of the MOI and isocyanate curing agent. After UV irradiating, the peel adhesion is decreased with increasing the amount of the MOI (Methacryloyloxyethyl isocyanate) and isocyanate curing agent, because of the high curing property.

• 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.

• Elastomers and Composites
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• v.45 no.4
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• pp.256-262
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• 2010

Dispersion polymerization of methyl acrylate, ethyl acrylate, butyl acrylate, and glycidyl methacrylate were performed in supercritical $CO_2$ at $80\;^{\circ}C$ and 346 bar. Glycidyl methacrylate linked poly(dimethylsiloxane) (GMS-PDMS) surfactant, which was prepared by linking glycidyl methacrylate to monoglycidyl ether terminated PDMS with amino-propyltriethoxysilane, was used as surfactant for the dispersion polymerization in $CO_2$. The yield of the poly(alkyl acrylate) polymers, synthesized in $CO_2$ medium, decreased as the alkyl tail of the acrylate monomers increased. Poly(glycidyl methacrylate) and poly(methyl acrylate) were produced in bead form whereas poly(ethyl acrylate) and poly(butyl acrylate) were viscous liquid. The poly(glycidyl methacrylate) particles had a number average diameter of 2.45 ${\mu}m$ and monodisperse distribution. The poly(methyl acrylate) had a number average diameter of 0.52 ${\mu}m$ and the particle size distribution was bimodal. The glass transition temperatures ($T_g$) of the poly(glycidyl methacrylate) and the poly(alkyl acrylate) products were 4~9 K higher than the $T_g$ of the corresponding acrylate polymers synthesized in conventional processes.

• Polymer(Korea)
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• v.34 no.1
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• pp.79-83
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• 2010

Alginate beads were prepared using poly(N-isopropylacrylamide-co-dimethylamino ethyl methacrylate)(P(NIPAM-co-DMAEMA)). First, P(NIPAM-co-DMAEMA) was immobilized on the surface of alginate beads by taking advantage of electrostatic interaction between alginate and P(NIPAM-co-DMAEMA). Second, P(NIPAM-co-DMAEMA) was contained in the matrix of alginate beads. P(NIPAM-co-DMAEMA) were prepared by a free radical polymerization at $74^{\circ}C$ for 12 h. The weight ratio of NIPAM to DMAEMA monomer was 95/5. The copolymer was identified by $^1H$-NMR. Releases from the alginate beads were observed at 30, 37, and $45^{\circ}C$ using blue dextran or FITC-dextran(fluorescein isothiocyanate-dextran) as a model drug. The effect of temperature on the degree of release from the beads was insignificant. FITC-dextran was released more than blue dextran possibly due to its smaller molecular weight.

• Journal of the Microelectronics and Packaging Society
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• v.10 no.4
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• pp.21-27
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• 2003

The copolymers with various composition of methyl methacrylate (MMA), ethyl methacrylate (EMA), methacrylic acid (MA) and hydroxyethyl methacrylate (HEMA) were synthesized for capacitive humidity sensitive materials. The capacitive humidity sensor consisted of a polymethacrylate film coated on both sides with gold electrode. Capacitance versus relative humidity increased with HEMA content in the copolymer. In the case of self-crosslinkable MMA/MA/HEHA= 40/10/10, the average capacitance at 30%RH, 60%RH and 90%RH are 102, 134 and 166 pF, respectively. And also, the hysteresis, temperature cycle and long-term stability were evaluated as a capacitance humidity sensor.

• Polymer(Korea)
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• v.30 no.2
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• pp.108-111
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• 2006

In this work, the effect of the hydrophobicity of acrylic polymers on the membrane morphology was investigated. The membranes were prepared with poly(methyl methacrylate) (PMMA), poly(ethyl methacrylate) (PEMA), poly (butyl methacrylate) (PBMA), poly(isobutyl methacrylate), and their blends using the wet phase inversion method. PMMA and PEMA having a relatively less hydrophobicity formed the channel-like structure, whereas PBMA and PIBMA having more hydrophobic units formed the finger-like structure. These morphological changes were attributed to differences in the solidification process of the polymer-rich phase determine d by the polymer/solvent/nonsolvent ternary phase diagram. The membrane structures of the blends were controlled by the main component of their blends.