• 한국안광학회지
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• 제13권3호
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• pp.29-34
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• 2008

목적: 본 연구에서는 HEMA(2-Hydroxyethyl methacrylate)/Silicone 기본 조합에 각각 BMA(Butyl methacrylate)와 MMA(Methyl methacrylate)를 혼합하여 콘택트렌즈의 재료로 사용한 후, 각각의 물리적 특성을 비교하였다. 방법: 캐스트 몰드 법을 이용하여 각각의 렌즈를 제조 하였으며, 각 시료의 물리적 특성에 대한 평균값을 사용하여 분석하였다. 결과: HEMA/silicone/BMA 조합의 경우, 함수율은 24.69%에서 29.26%, 인장강도는 0.109 kgf에서 0.263 kgf의 분포를 나타내었다. HEMA/silicone/MMA 조합의 경우, 팽윤율은 13.56%에서 14.83%, 함수율은 25.61%에서 29.33%, 인장강도는 0.107 kgf에서 0.286 kgf의 분포를 나타내었다. 결론: 두 조합은 HEMA/silicone(0.20%~11.50%)의 기본 조합에서 BMA(5.15%)와 MMA(5.15%)를 일정량 첨가한 것으로 두 경우 모두에서 BMA의 양과 MMA의 양이 상대적으로 감소할수록 팽윤율과 함수율이 증가하는 경향을 보였다. HEMA/silicone/MMA 조합의 경우, 인장강도는 silicone의 비율이 증가할수록 4-MMA 시료까지는 다소 증가하는 경향을, HEMA/silicone/BMA 조합의 경우, 인장강도는 silicone의 비율이 증가할수록 감소하는 경향을 나타내었다.

• Elastomers and Composites
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• 제24권4호
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• pp.265-275
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• 1989

The graft copolymerizations of acrylonitrile (AN) and methyl methacrylate (MMA) onto chloroprene rubber (CR) were carried out with benzoyl peroxide(BPO) as an initiator. The effect of solvent, mole ratio of AN to MMA, reaction time and temperature, and initiator concentration on graft copolymerization were examined. It was observed that the grafting efficiency increased as increasing mole ratio of AN to MMA. the graft copolymer, acrylonitrile- CR-methyl methacrylate (ACM), was identified by infrared spectroscopy and morphology. Thermal stability of ACM was found to be improved when compared with those of CR.

• Journal of Electrical Engineering and Technology
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• 제6권6호
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• pp.836-841
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• 2011

Plasma polymerized methyl methacrylate (ppMMA) thin films were deposited by plasma polymerization technique with different plasma powers and subsequently thermally treated at temperatures of 60 to $150^{\circ}C$. To find a better ppMMA preparation technique for application to organic thin film transistor (OTFT) as dielectric layer, the chemical composition, surface morphology, and electrical properties of ppMMA were investigated. The effect of ppMMA thin-film preparation conditions on the resulting thin film properties were discussed, specifically O-H site content in the pMMA, dielectric constant, leakage current density, and hysteresis.

• Macromolecular Research
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• 제15권4호
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• pp.302-307
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• 2007

The living radical polymerization of methyl methacrylate (MMA) by atom transfer radical polymerization, (ATRP) employing a $Fe(II)X_2/diphenyl-2-pyridyl$ phosphine (PyP) catalytic system (X=Cl, Br), was investigated using several initiators and solvents at various temperatures. Most of the polymerizations with the PyP ligand were well controlled, with a linear increase in the number average molecular weights ($M_n$) vs. conversion, with relatively low molecular weight distributions ($M_w/M_n=1.2-1.4$) throughout the reactions. The measured weights matched those of the predicted values. The ethyl-2-bromoisobutyrate (EBriB) initiated ATRP of MMA, with the $Fe(II)X_2/diphenyl-2-pyridyl$ phosphine catalytic system (X=Cl, Br), was better controlled in p-xylene at $80^{\circ}C$ than the other solvents used in this study.

• 한국소성가공학회:학술대회논문집
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• 한국소성가공학회 2004년도 춘계학술대회 논문집
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• pp.152-155
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• 2004

Effects of sliding speed, applied load, counterpart radius and thickness of PMMA (Poly Methyl Methacrylate) coating layers on their dry sliding frictional and wear behavior were investigated. Sliding wear tests were carried out using a pin-on-disk wear tester. The PMMA layer was coated on Si wafer by a sol-gel technique with two different thicknesses, $1.5{\mu}m\;and\;0.8{\mu}m$. AISI 52100 bearing steel balls were used as a counterpart of the PMMA coating during the wear. Normal applied load and sliding speed were varied. Wear mechanisms were investigated by examining worn surfaces by an SEM. Under most of sliding test conditions, the thicker layer with the thickness of $1.5{\mu}m$ showed lower fiction coefficient than the thinner layer. Effects of sliding speed and counterpart's radius on the frictional behavior were varied depending on the thickness of the coating layer.

• 한국가구학회지
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• 제14권1호
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• pp.11-20
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• 2003

Wood cell-wall modification with acetic anhydride, lumen filled with styren monomer and methyl methacrylate, and a combination of these two treatments were studied for their effectiveness for dimensional stability. Compared to those of untreated Pinus densiflora Sieb. et Zucc and sole acetylated red pine, The combination of acetylation and impregnation with methy methacrylate greatly reduced water absorption, increased ASE to the best and gave better bending strength and compression strength.

• Bulletin of the Korean Chemical Society
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• 제35권10호
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• pp.2929-2934
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• 2014

The reaction between $[CdBr_2{\cdot}4H_2O]$ and anhydrous $[ZnCl_2]$ with N,N'-bidentate N-(pyridin-2-ylmethylene)-cyclopentanamine (impy) in ethanol yields dimeric $[(impy)Cd({\mu}-Br)Br]_2$ and monomeric $[(impy)ZnCl_2]$ complexes, respectively. The X-ray crystal structure of Cd(II) and Zn(II) complexes revealed that the cadmium atom in $[(impy)Cd({\mu}-Br)Br]_2$ and zinc in $[(impy)ZnCl_2]$ formed a distorted trigonal-bipyramidal and tetrahedral geometry, respectively. Both complexes showed moderate catalytic activity for the polymerisation of methyl methacrylate (MMA) in the presence of modified methylaluminoxane (MMAO), with polymethylmethacrylate (PMMA) syndiotacticity of about 0.70.

• 한국응용과학기술학회지
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• 제2권2호
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• pp.31-38
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• 1985

The transesterification reaction between ethanolamine and methyl-methacrylate was kinetically investigated in the presence of various metal acetate catalysts at $110^{\circ}C$. The transesterification was found to obey first-order kinetice with respect to the concentration of ethanolamine and methyl-methacrylate, respectively. By the Arrhenius plot, the activation energy has been calculated as 11.9 Kcal with lead acetate catalyst, 14.7 Kcal without catalyst. The reactivities has highest value where the electronegativity and instability constant (Kij) values for the metal acetate catalysts are about 1.6.

• Elastomers and Composites
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• 제28권3호
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• pp.191-197
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• 1993

The graft copolymerization of methyl methacrylate(MMA) onto natural rubber latex(NRL) initiated by t-butyl hydroperoxide(t-BHPO) was investigated in aquous medium. The grafting percentage, grafting efficiency and total conversion were observed in various reaction conditions such as monomer, initiator and emulsifier concentration, reaction temperature, reaction time and agitation speed. The optimum conditions for the graft copolymerization onto natural rubber latex were as follows ; At given monomer concentration of $3{\times}10^{-2}mole/l$, the maximum grafting percentage was appeared in the case of grading in initiator concentration of $4{\times}10^{-2}mo1e/l$ and emulsifier concentration of 0.2wt.% at $40^{\circ}C$ for 5hrs.

• Bulletin of the Korean Chemical Society
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• 제19권6호
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• pp.625-628
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• 1998

The dynamic mechanical properties of the unclustered cesium neutralized poly(methyl methacrylate-co-methacrylic acid) ionomers plasticized with three different plasticizers of low molecular weight were investigated. It was found that the effectiveness of the plasticization followed the order: glycerol (Gly) 4-decylaniline (4DA) >dioctyl phthalate (DOP). For the ionomer plasticized with Gly, the only effect was a significant decrease in the Tg. Thus it is concluded that the polar plasticizer not only increases the mobility of the ionomer but also dissolves the ionic groups. In the case of the 4DA-plasticized ionomer, both a drastic decrease in the Tg and the appearance of a second glass transition were observed. Therefore, it is suggested that the nonpolar 4DA molecules partition evenly in the poly(methyl methacrylate) matrix and cluster phases via hydrogen bonding between the aniline group of the plasticizer and the carbonyl groups of the ionomer. As a result, the Tg is lowered, multiplets can form, and the material behaves like a clustered ionomer.