• Bulletin of the Korean Chemical Society
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• 제18권9호
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• pp.958-961
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• 1997

The compatibility and the surface structure of blends of poly(styrene-co-acrylonitrile) (SAN) with either poly(methyl methacrylate) (PMMA) or hydrolyzed PMMA (H-PMMA) were studied in terms of film thickness, interaction, and surface free energy difference on the basis of X-ray photoelectron spectroscopy (XPS), attenuated total reflection Fourier transform IR spectroscopy and atomic force microscopy. The XPS measurement showed that the surface enrichment of (PMMA/SAN) blends with different AN contents of SAN and with different carboxyl acid contents of PMMA was dependent on the molecular interaction, the surface free energy difference between components and the sample preparation history. It was found that the compatibility of H-PMMA and SAN was reduced with increasing carboxyl acid content of PMMA.

• 소성∙가공
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• 제13권8호
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• pp.716-722
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• 2004

Effects of sliding speed, applied load, 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 spin coating process with two different thicknesses, $1.5\mu\textrm{m}$ and $0.8\mu\textrm{m}$. 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 of the coatings were investigated by examining worn surfaces using an SEM. Friction coefficient of the coatings decreased with the increase of the applied load. Both adhesion and deformation of the coating determined the coefficient. The thicker PMMA layer with the thickness of $1.5mutextrm{m}$ showed lower friction coefficient than the thinner layer under most test conditions. Effects of sliding speed and applied load on the frictional behavior were varied depending on the thickness of the coating layer.

• Macromolecular Research
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• 제13권2호
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• pp.102-106
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• 2005

Poly(methyl methacrylate) (PMMA)/sodium montmorillonite (Na-MMT) nanocomposites were prepared with a novel method utilizing a macroazoinitiator (MAI). To induce the intergallery polymerization of methyl methacrylate (MMA), the MAI containing a po1y(ethylene glycol) (PEG) segment was intercalated between the lamellae of Na-MMT and swelled with water to enhance the diffusion of MMA into the gallery. The structure of the nanocomposite was examined using X-ray diffraction and transmission electron microscopy, and the thermal properties were examined using differential scanning calorimetry and thermogravimetry. The PMMA/Na-MMT nanocomposite prepared by intergallery polymerization showed a distinct enhancement of its thermal properties; an approximately $30^{\circ}C$ increase in its glass transition temperature and an $80\sim100^{\circ}C$ increase in its thermal decomposition temperature for a $10\%$ weight loss.

• 폴리머
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• 제37권2호
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• pp.177-183
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• 2013

본 연구에서는 poly(ethylene terephthalate)(PET) 필름을 기재로 하여 분산코팅에 의해 형성된 poly(vinylidene fluoride)(PVDF)와 poly(methyl methacrylate)(PMMA) 블렌드 코팅의 표면 특성을 관찰하였다. 분산코팅의 특성상 저온에서 형성된 블렌드 코팅은 PVDF 입자의 형태와 결정구조가 그대로 유지되었으나 $120^{\circ}C$ 이상의 코팅온도에서 형성된 코팅의 경우 블렌드에 포함되어 있는 PVDF의 양에 따라 다양한 표면 특성을 나타내었다. 블렌드 중 PVDF의 양이 80 wt% 이상인 경우 PVDF의 ${\alpha}$-결정구조에 의한 특성이 확실히 관찰되는 반면에 PMMA의 양이 증가하면 표면 형태와 결정구조의 변화가 변화하는 것을 관찰하였다. 또한 코팅층의 최외각 표면에 대한 XPS 분석결과는 분산코팅에서도 PVDF의 표면 이행성이 나타남을 보여준다.

• 한국자원리싸이클링학회:학술대회논문집
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• 한국자원리싸이클링학회 2005년도 추계정기총회 및 제26회 학술발표대회 고분자리싸이클링기술 특별심포지엄
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• pp.360-367
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• 2005

PMMA는 우수한 물성으로 인하여 각종 소재 및 건축자재로 널리 활용되고있다. PMMA는 열 분해시 모노머 단위가 일정하게 이탈하는 unzip reaction을 나타내어 모노머로의 회수가 용이한 특징을 가지고있다. PMMA를 열분해하여 MMA를 회수하기 위한 기초연구로써 본 연구에서 TGA를 이용한 열분해특성을 조사하였다.

• Nuclear Engineering and Technology
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• 제52권11호
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• pp.2613-2619
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• 2020

This work investigated the gamma-ray shielding performance, and the physical and mechanical properties of poly (methyl methacrylate) (PMMA) composites embedded with 0-44.0 wt% bismuth trioxide (Bi₂O₃) fabricated by the fast ultraviolet (UV) curing method. The results showed that the addition of Bi₂O₃ had significantly improved the gamma shielding ability of PMMA composites. Mass attenuation coefficient and half-value layer were examined using five gamma sources (Cs-137, Ba-133, Cd-109, Co-57, and Co-60). The high loading of Bi₂O₃ in the PMMA samples improved the micro-hardness to nearly seven times that of the pure PMMA. With these enhancements, it was demonstrated that PMMA/Bi₂O₃ composites are promising gamma shielding materials. Furthermore, the fast UV curing exerts its great potential in significantly shortening the production cycle of shielding material to enable rapid manufacturing.

• 유변학
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• 제10권4호
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• pp.247-255
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• 1998

이축 압출기에서 삼성분계 블렌드가 용융 혼련될 때 상구조의 형성과정에 대하여 연구하였다. 삼성분계 블렌드의 연속상은 polycarbonate(PC)로 고정하였고 나머지 분산상을 이루는 성분으로는 acrylonitrile-butadiene-styrene(ABS), methyl methacrylate-butadiene-ethyl acrylate(MBE), styrene-acrylonitrile(SAM) 공중합체, 그리고 poly(methyl methacrylate)(PMMA)를 사용하였다. 블렌드의 여러 가지 조성에 따라 최종 상구조는 현저한 차이를 보였고 특히 MBE와 PMMA의 경우는 각각 PC-SAN의 계면에 선택적으로 위치하였다. 삼성분계 고분자 블렌드의 상구조 형성과정은 성분간의 계면장력과 합체 현상의 상호 작용에 의하여 지배되었으며 합체의 정도는 계면에서의 점도에 의하여 민감하게 변화되었다.

• 대한화학회지
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• 제24권3호
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• pp.259-265
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• 1980

자유라디칼 telomerization 반응을 이용하여 스티렌-메타크릴산메틸 block 혼성중합체 (PS-b-PMMA)를 합성하였다. AIBN을 개시제로 사용하여 CCI$_4$로 스티렌을 telomerization시킨 다음 생성된 중합체의 $CCI_3$ 말단기를 macrotelogen으로 사용하여 AIBN 개시에 의해 메타크릴산 메틸을 다시 telomerization하여 스티렌-메타크릴산메틸 block 혼성중합체를 얻었다. Macrotelogen의 농도, 단위체의 농도, macrotelogen의 분자량, 반응온도 및 용매의 농도가 block 혼성중합체생성에 미치는 영향을 조사하였다. 반응조건을 조절하여, PMMA가 약 10무게%까지 포함된 block 혼성중합체를 얻었다.

• Elastomers and Composites
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• 제23권4호
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• pp.289-298
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• 1988

The thermal degradation of poly(methyl methacrylate)(PMMA) and poly($\alpha$-methylstyrene-co-acrylonitrile)(SAN) mixtures were carried out using the thermogravimetry(TG) and differential scanning calorimetry(DSC) in the stream of nitrogen and air with 50 ml/min at the various heating rate from 4 to $20^{\circ}C/min$ and temperature from 20 to $500^{\circ}C$. The value of activation energies of thermal degradation determined by TG and DSC in the various PMMA/SAN mixtures were 34-54 kcal/mol in the stream of nitrogen. The value of activation energy of SAN 60% mixture were appeared high in comparison with addition rule. PMMA/SAN mixtures by the analysis of infrared spectrophotometer were decomposed by main chain scission in the stream of nitrogen.

• Elastomers and Composites
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• 제24권1호
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• pp.11-18
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• 1989

The thermal degradation of Poly(methyl methacrylate) (PMMA) and poly(acrylonitrile butadiene styrene)(ABS) terpolymer as well as their mixtures were carried out using the thermogravimetry and differential scanning calorimetry(DSC) in the stream of nitrogen and air with 50 ml/min at the various heating rate from 4 to $20^{\circ}C/min$ and temperature from 200 to $300^{\circ}C$ The values of activation energies of thermal degradation determined by TG and DSC in the various PMMA/ABS mixtures were $34{\sim}58Kcal/mol,\;35{\sim}54Kcal/mol$ in the stream of nitrogen. The values of activation energy of ABS20% mixture was appeared high in camparison with addition rule. According to increasing the composition of ABS, the temperatures of glass transition and initial decomposition temperature were increased. PMMA/ABS mixtures by the analysis of infrared spectrophotometer were decomposed by main chain scission in the stream of nitrogen.