• 제목/요약/키워드: poly-methyl methacrylate

검색결과 339건 처리시간 0.032초

PEG를 포함한 실리콘 수화젤 렌즈의 제조 및 특성 (Preparation and Characterization of Silicone Hydrogel Lens Containing Poly(ethylene glycol))

  • 장하나;정연복;김승수
    • 폴리머
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    • 제33권2호
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    • pp.169-174
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    • 2009
  • Poly(ethylene glycol)(PEG)이 콘택트렌즈에 미치는 영향을 조사하기 위하여 PEG가 도입된 실리콘 수화젤 렌즈를 제조하고 특성을 평가하였다. 실리콘 수화젤 렌즈는 methacryloxypropyl tris(trimethylsiloxy) silane(TRIS), methyl methacrylate(MMA), N,N'-dimethyl acrylamide(DMA) 등과 PEG 함유 단량체인 poly(ethylene glycol) methyl ether methacrylate(PEG-MEM)를 공중합하여 제조하였다. 특성평가는 Fourier transform infrared spectroscopy(FT-IR), electron spectroscopy of chemical analysis(ESCA), scanning electron microscopy(SEM) 등과 물 흡수도, 물 접촉각, 광투과도, 인장강도 등을 평가하였고 단백질 흡착 실험을 행하였다. FT-IR 및 ESCA 분석결과 C-O 결합피크의 증가를 보여 PEG 도입을 확인하였고 SEM 분석결과 상분리 현상은 나타나지 않았다. 물흡수도는 PEG-MEM의 도입에 따라 1차적으로 증가하였고 물 접촉각 및 광투과도는 감소하는 현상을 나타내었다. 단백질흡착 실험결과, PEG의 도입에 따라 눈물 속에 있는 단백질인 albumin, lysozyme, $\gamma$-globulin 등의 흡착이 감소하는 현상을 나타내었다. 또한 PEG 분자량의 증가에 따라 흡착되는 단백질의 양이 감소하는 것을 확인할 수 있었다. 인공눈물을 사용한 단백질 흡착실험에서도 PEG의 도입에 따라 단백질 흡착이 감소하는 현상을 나타내었다.

고분자 필름이 코팅된 QCM 시스템에 의한 방향족 화합물의 흡착 (Adsorption of Aromatic Compounds on a QCM System Coated with Polymer Films)

  • 황민진;심왕근;문희
    • Korean Chemical Engineering Research
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    • 제51권2호
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    • pp.233-239
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    • 2013
  • Poly(isobutylene), polystyrene 및 poly(methyl methacrylate)로 코팅된 quartz crystal microbalance(QCM) 시스템을 구성하여, 매우 낮은 압력에서 benzene, toluene, p-xylene의 흡착량을 측정하였다. 모든 흡착실험에서 QCM 시스템의 공진 주파수 변화는 압력의 증가에 비례하였다. 실험결과로부터 각각의 고분자 필름에 대한 흡착물질의 Henry 상수를 구하였으며 고분자 필름과 흡착물질 사이의 최소 흡착 포텐셜 에너지와 비교하였다. 전체적으로 흡착량과 최소 흡착 포텐셜 에너지는 명백한 상관관계가 있었다.

Thermally Robust Highly Crosslinked Poly(methyl methacrylate-co-divinyl benzene) Microspheres by Precipitation Polymerization

  • Shim, Sang-Eun;Sunhye Yang;Hyejeon Jung;Soonja Choe
    • Macromolecular Research
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    • 제12권2호
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    • pp.233-239
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    • 2004
  • We prepared thermally robust fully crosslinked poly(methyl methacrylate-co-divinyl benzene) [poly(MMA-co-DVB)]microspheres successfully by precipitation polymerization in the absence of a stabilizing agent. The DVB concentration plays a pivotal role not only in the formation of the individually stable microspheres but also in the polymerization characteristics, including the particle size, the uniformity of size, the polymerization yield, and the thermal properties. The number-average diameter of the microspheres increased linearly, from 0.72 to 2.15 $\mu\textrm{m}$, and the particle size distribution became narrower, by elevating the uniformity from 1.35 to 1.12, as the DVB concentration increased from 20 to 75 mol%. In addition, the yield of the polymerization increased, from 73.4 to 98.6%, as the DVB concentration increased. Since the prepared particles possess fully crosslinked microstructures, no glass transition temperatures were observed, but all the samples prepared with DVB concentrations ranging from 20 to 75 mol% possess enhanced thermal properties. Based on the DSC and TGA data, the thermal stability of the mesospheres prepared by the precipitation polymerization is significantly improved as a result of crosslinking with DVB.

폴리(메틸 메타크릴레이트)-폴리스티렌 이종 블록 공중합체/폴리(비닐리덴 플루오라이드) 블렌드의 미세 상분리와 결정화 (Microphase Separation and Crystallization in Binary Blends Consisting of Poly (methyl methacrylate)-block-Polystyrene Copolymer and Poly (vinylidene fluoride))

  • 김지선;이광희;조성무;류두열;김진곤
    • 폴리머
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    • 제28권6호
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    • pp.509-518
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    • 2004
  • 비대칭 블록 공중합체와 단일고분자로 구성된 블렌드의 미세 도메인 구조와 결정화 거동을 소각 X-선 산란, 광학 현미경 및 DSC를 사용하여 조사하였다. 본 연구에서는 폴리(메틸 메타크릴레이트) 블록의 무게 분률이 0.53인 폴리(메틸 메타크릴레이트)-폴리스티렌 이종 블록 공중합체 (PMMA-b-PS)를 저분자량 폴리(비닐리덴 플루오라이드) (PVDF)와 혼합하였다. PVDF 함량 증가에 따라 블렌드 미세구조가 라멜라에서 실린더 구조로 전이하였으며, PVDF의 결정화는 결정화 이전에 형성된 미세구조의 배열을 교란시켜 질서도가 낮은 형태를 야기시켰다. 또한, PVDF 결정화 거동은 PMMA 블록과의 혼화성 및 미세 도메인에 의해 부가되는 공간적 제한에 큰 영향을 받았다.

Size and Uniformity Variation of Poly(MMA-co-DVB) Particles upon Precipitation Polymerization

  • Yang, Sun-Hye;Shim, Sang-Eun;Lee, Hui-Je;Kim, Gil-Pyo;Choe, Soon-Ja
    • Macromolecular Research
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    • 제12권5호
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    • pp.519-527
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    • 2004
  • Stable poly(methyl methacrylate-co-divinylbenzene) (poly(MMA-co-DVB)) microspheres were prepared by precipitation polymerization using acetonitrile as the main medium under various polymerization conditions, including modifications of the agitation speed, monomer and initiator concentrations, DVB content in the monomer mixture, and the use of various cosolvents. Gentle agitation was required to obtain smooth spherical particles. The individually stable microspheres were obtained at monomer concentrations of up to 15 vol% in an acetonitrile medium. The number-average diameter increased linearly with respect to increases in the monomer and initiator concentrations. We found, however, that the uniformity of the microspheres was independent of the variation of the polymerization ingredients because nuclei formation was solely influenced by the crosslinking reaction of the monomers. We obtained higher yields for the polymerization at higher concentrations of monomer and initiator. The concentration of DVB in the monomer mixture composition played an important role in determining not only the size of the microspheres but also the yield of the polymerization. In addition, although we employed various cosolvents as the polymerization medium, we found that acetonitrile/2-methoxyethanol was the only system that provided spherical particles without coagulation. This finding indicates that the precipitation polymerization is strongly dependent on the solvent used as the medium.

Fourier-Transform Infrared and Calorimetric Studies about the Influence of Tacticity of Poly(methyl methacrylate) on the Compatibility with Poly(ethylene oxide)

  • John, Eun-Sook;Jeon, Seung-Ho;Ree, Taik-Yue
    • Bulletin of the Korean Chemical Society
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    • 제10권2호
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    • pp.123-128
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    • 1989
  • Calorimetric study in conjunction with Fourier-transform infrared (FTIR) spectroscopic study was carried out on the blends of poly(ethylene oxide) (PEO) with isotactic, atactic and syndiotactic poly(methyl methacrylate) (i-, a-, and s-PMMA). From the differential scanning calorimetric (DSC) measurements, the three types of blends show a depression of the melting temperatures. This indicates that PEO is compatible with i-, a-, and s-PMMA. But the largest melting point depressions of PEO are always found in the blends with s-PMMA. For PEO/a-PMMA and PEO/s-PMMA, the degree of crystallinity as a function of composition deviates substantially from that of the ideal blend in which no interaction between the components exists. The FTIR spectra of all three types of blends are recorded. In order to observe the microstructural changes of PEO in blends, we analyzed the spectra using digital weighted subtraction and addition techniques. It was concluded that the microstructures of PEO are strongly perturbed by the PMMA's. Among these blends PEO microstructure in PEO/s-PMMA blends is most greatly influenced. It indicates that the blending is most preferred with s-PMMA than a- and i-PMMA. It can be explained on the basis of the molecular structure of PMMA's.

4차 암모늄염 촉매를 이용한 Poly(GMA)에의 이산화탄소 직접 고정화 (Direct Incorporation of Carbon Dioxide to Poly(GMA) Using Quaternary Ammonium Salt Catalysts)

  • 성충기;김경훈;문정열;천승우;나석은;박대원
    • 공업화학
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    • 제10권1호
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    • pp.129-134
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    • 1999
  • 4차 암모늄염 촉매 존재하에서 poly(glycidyl methacrylate)[poly(GMA)]에 이산화탄소를 직접 부가시켜 poly[(1,3-dioxolane-2-oxo-4-yl)methyl methacrylate][poly(DOMA)]를 합성하였다. 4차 암모늄염 촉매는 높은 이산화탄소 고정화 효율을 나타내었으며, 양이온의 크기가 클수록, 짝음이온의 친핵성이 강할수록 높은 촉매 활성을 나타내었다. 또한 반응온도가 높을수록 높은 이산화탄소 부가율을 나타내었다. 한편 고압 회분 반응기에서 이산화탄소의 압력변화를 관찰함으로써 실시한 속도론적 고찰 결과 반응속도는 poly(GMA)와 이산화탄소의 농도에 대하여 각각 1차 반응이었고, 이때 반응속도상수 k는 $0.69L/mol{\cdot}h$이었다. DMSO를 용매로 사용한 경우 $80^{\circ}C$에서의 $CO_2$의 Henry 상수 H'는 $6.8{\times}10^{-4}mol/L{\cdot}KPa$로 나타났다.

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Polymer blending에 따른 TIPS-Pentacene의 특성 변화 (The electrical properties change of TIPS-Pentacene due to polymer blending)

  • 임창윤;김영훈;한정인
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2011년도 제42회 하계학술대회
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    • pp.1499-1500
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    • 2011
  • In this paper, we investigated the electrical properties change of 6,13-bis(triisopropyl-silylethynyl) pentacene (TIPS-pentacene) depending on polymer blend. We fabricated organic thin film transistor (OTFT) using blending solution of small molecule and polymer. In this study poly(2-methoxy-5-(2-ethyl-hexyloxy)-1,4-phenylene-vinylene) (MEH-PPV), poly (9-vinylcarbazole) (PVK), poly [N,N'-bis(4-butylphenyl)-N,N'-bis(phenyl)benzidine] (poly-TPD), poly(${\alpha}$-methyl styrene), Poly(methyl methacrylate) (PMMA) are used as a polymer. Fabricated OTFT with blending solution of TIPS-pentacene and PVK shows best performance in this experiment. OTFT fabricated by blending solution of TIPS-pentacene and PVK shows field effect mobility of 0.0189 $cm^2/V{\cdot}s$, on/off ratio of 1.9E-5 and threshold voltage of 7.4 V.

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