• Macromolecular Research
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• 제16권2호
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• pp.120-127
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• 2008

Glycidyl methacrylate linked poly(dimethylsiloxane) (GMA-PDMS) was synthesized and used as a stabilizer for the dispersion polymerization of methyl methacrylate (MMA) in supercritical $CO_2$. This study examined the effect of the concentrations of the stabilizer, 2,2'-azobisisobutyronitrile (AIBN) initiator, and MMA on the yield, molecular weight, and morphology of the poly(methyl methacrylate) (PMMA) product. PMMA was obtained in 94,6% yield using only 0,87 wt% GMA-PDMS, When the AIBN concentration was increased from 025 to 1.06 wt%, the molecular weight and particle size of the PMMA decreased from 56,600 to 21,600 and from 4.1 to $2.7{\mu}m$, whereas the particle size distribution increased from 1.3 to 1.9. The $M_n$ of the PMMA product ranged from 41,600 and 55,800 under typical polymerization conditions. The PMMA particle diameter ranged from 1.8 to $11.0{\mu}m$ and the particle size distribution ranged from 1.4 to 1.8.

• 한국정밀공학회지
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• 제31권5호
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• pp.441-449
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• 2014

Thermoplastic fusion bonding is widely used to seal polymer microfluidic devices and optimal bonding protocol is required to obtain a successful bonding, strong bonding force without channel deformation. Besides, UV modification of the PMMA (poly-methyl methacrylate) is commonly used for chemical or biological application before the bonding process. However, study of thermal bonding for the UV modified PMMA was not reported yet. Unlike pristine PMMA, the optimal bonding parameters of the UV modified PMMA were $103^{\circ}C$, 71 kPa, and 35 minutes. A very low aspect ratio micro channel (AR=1:100, $20{\mu}m$ depth and $2000{\mu}m$ width) was successfully bonded (over 95%, n>100). Moreover, thermal bonding of multi stack PMMA chips was successfully demonstrated in this study. The results may applicable to fabricate a complex 3 dimensional microchannel networks.

• 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.

• 한국복합재료학회:학술대회논문집
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• 한국복합재료학회 2003년도 추계학술발표대회 논문집
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• pp.29-32
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• 2003

Multi -walled carbon nanotube(MWNT)/poly(methyl methacrylate) composites were fabricate d through film casting. Manufacturing process was established using a ultrasonic cleaner and a homogenizer. Acetone was used as a solvent to melt PMMA and mix with MWNT. The ultrasonic cleaner performed an important role in producing MWNT/MMA nanocomposites. Ultrasonic energy was utilized to disperse MWNT in acetone. Also, melting PMMA in acetone and mixing MWNT and PMMA were achieved using the homogenizer. It was confirmed that the nanohlbes were well dispersed in PMMA according to SEM images.

• 폴리머
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• 제30권1호
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• pp.90-94
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• 2006

다중벽 탄소 나노튜브(multi-walled carbon nanotubes, MWNTs)를 포함하고 있는 poly(methyl methacrylate)(PMMA) 나노섬유를 전기 방사법에 의해 제작하였다. 주사 전자 현미경을 통하여 용매의 종류(dimethyl formamide, chloroform and toluene)와 탄소 나노튜브의 함량(0.5 and $3.0\;wt\%$)에 의해 나노섬유 표면의 형상과 탄소 나노튜브와 나노섬유의 구조가 영향을 받았다. 집적판의 전극 모양을 조절함으로써 나노섬유의 정렬이 가능하였다. 고분자 사슬의 회전 반경과 탄소 나노튜브의 크기의 비교를 통하여 PMMA 나노섬유와 탄소 나노튜브의 관계를 정리하였다. 탄소 나노튜브 투입량이 증가함에 따라 고분자 비드가 증가하였다.

• Macromolecular Research
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• 제8권6호
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• pp.292-297
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• 2000

The theoretical synthesis of the isotactic and syndiotactic poly(methyl methacrylate) were carried out as a model for real polymerization reactions following the normal chain reaction processes by repeating the uniform localization of wave functions with inclusion of the interaction between the end group of the cluster and an attaching molecule by the elongation method, and then, the calculated value was compared with the usual PM$_3$ calculation. The results revealed that a reaction of cluster with monomer molecules has made it possible to calculate the electronic structure and total energy of polymer with nearly infinite length and a matrix of constant dimension. The isotactic poly(methyl methacrylate) is more stable than syndiotactic one. The same tendency have been found between the experimentally measured properties and a calculated total energy to explain the chain motion in isotatic and syndiotactic poly(methyl methacrylate).

• Macromolecular Research
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• 제15권7호
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• pp.617-622
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• 2007

A simple and economic antistatic agent, (2-methacryloyloxyethyl)acid phosphate (acryl phosphate), was synthesized via the reaction of 2-hydroxyethyl methacrylate with phosphorus pentoxide. The acryl phosphate antistatic agent, synthesized in this study, was introduced into poly(methyl methacrylate) (PMMA) resin via copolymerization with MMA. This antistatic agent provides the PMMA matrix with excellent antistatic properties, including surface resistance and electric charge. A comparison of the present antistatic agent with other commercial agents demonstrated the excellence of not only its electrical, but also its thermal and mechanical properties.

• 멤브레인
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• 제20권3호
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• pp.203-209
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• 2010

원자전달 라디칼 중합을 이용하여 poly(epichlorohydrine) (PECH)를 주사슬로 한 양친성 가지형 공중합체를 합성하였다. PECH로부터 poly(methyl methacrylate)(PMMA) 및 poly(butyl methacrylate)(PBMA)의 가지형 중합이 성공적임을 $^1H$ NMR과 FT-IR분석을 통해 확인하였다. 합성한 가지형 공중합체에 KI나 LiI 염을 도입하였을 때, ether 신축진동 피크가 낮은 wavenumber영역으로 이동하였으며, 이는 배위결합 상호작용 때문이다. PECH-g-PBMA 복합체의 이온 전도도는 PECH-g-PMMA 복합체에 비해 항상 높게 나타났는데, 이는 고무상인 PBMA 사슬의 높은 이동성으로부터 기인한 것으로 확인되었다. 최고 이온전도도 값은 질량비 10 wt%의 KI가 도입된 PECH-g-PBMA 전해질체에서 $2.7{\times}10^{-5}\;S/cm$로 나타났다.

• Advances in materials Research
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• 제2권2호
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• pp.99-109
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• 2013

In the present investigation, nanocomposite films with poly(methyl methacrylate) (PMMA) as a polymer matrix and barium titanate as a filler were prepared by solution casting method. Barium titanate nano particles were prepared using Ti(IV) triethanolaminato isopropoxide and hydrated barium hydroxide as precursors and tetra methyl ammonium hydroxide (TMAH) as a base. The nanocomposite films were characterized using XRD, FTIR, SEM and dielectric spectroscopy techniques. Dielectric measurements were performed in the frequency range 100 Hz-10 MHz. Dielectric constant of nanocomposites were found to depend on the frequency, the temperature and the filler fraction. Dissipation factors were also influenced by the frequency and the temperature but not much influenced by the filler fractions. The 10 wt% of BT-PMMA nanocomposite had the lowest dielectric constant of 3.58 and dielectric loss tangent of 0.024 at 1MHz and $25^{\circ}C$. The dielectric mixing model of Modified Lichtenecker showed the close fit to the experimental data.

• 접착 및 계면
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• 제2권1호
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• pp.18-22
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• 2001

Poly(vinylidene fluoride)(PVDF)를 포함하는 고분자 블렌드 필름의 표면층의 모폴로지를 원자력간 현미경과 시차주사열량계 측정을 토대로 연구하였다. ${\alpha}$ 및 ${\gamma}$형 결정상을 가진 PVDF는 Poly(methyl methacrylate)(PMMA) 및 가수분해된 PMMA(carboxyl content:14wt%)와의 블렌딩에서 표면층은 PVDF의 결정상만으로 이루어져 있음을 확인하였다. 그러나 PMMA의 결정상이 가수분해율이 증가함에 따라 표면 자유에너지의 차이도 증가함에도 불구하고 가수분해된 PMMA의 존재를 확인하였다. 이러한 결과는 표면층에서의 낮은 표면 자유에너지 성분인 PVDF의 농축 정도는 자유에너지 차보다 상호작용력의 크기에 밀접히 관련되어 있음을 알 수 있었다. 한편, carboxyl group의 도입은 PVDF와 PMMA의 상용성을 저해하는 것으로 밝혀졌다.