• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1996년도 추계학술대회 논문집
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• pp.225-229
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• 1996

In this study, in order to develop outdoor insulating materials, SIN(simultaneous interpenetrating polymer network) was introduced to Epoxy resin and the environment resistance was investigated. The single network structure specimen(E series) formed of Epoxy resin alone and simultaneous interpenetrating polymer network specimen (EM series) in which epoxy resin was taken as the first network and methyl methacrylate resin as the second network were manufactured. Ten kinds of specimens were manufacture by filler (SiO$_2$) content. SEM were utilized in order to confirm their network structure changes, and AC voltage dielectric strength was measured. Also, UV-test and tracking test were carried out investigate the environment resistance characteristic. Therefore the variations of network structure were happened as a result of SEM test, and it was confirmed that simultaneous interpenetrating polymer network specimens were more excellent than single network structure specimens.

• Carbon letters
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• 제7권4호
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• pp.266-270
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• 2006

Multi-walled carbon nanotube-poly methyl methacrylate (MWNT/PMMA) nanocomposite has been prepared by in situ polymerization of MMA dispersed with MWNTs. The MWNTs were functionalized by nitric acid and sulfuric acid treatment, and this was confirmed by FTIR spectrometer. The solution mixture of MWNTs and MMA was partially polymerized at $80^{\circ}C$, followed by the addition of AIBN and polymerization at $50^{\circ}C$. The MWNT-PMMA composite was prepared by casting the pre-polymer on the glass plate, and the optical properties have been studied using UV-vis spectrometer. The acid treated MWNTs were well dispersed in MMA with fairly good dispersion stability, while flocculation and sedimentation was observed from raw MWNTs in MMA.

• Elastomers and Composites
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• 제55권4호
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• pp.314-320
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• 2020

This study focused on experiments with polyethylene glycol (PEG) and glycidyl methacrylate (GMA), which are functional additives for water-expandable rubber. Polychloroprene rubber (CR)/superabsorbent polymer (SAP) composites were prepared and their cure behaviors, mechanical properties, water absorption rates, and surface morphology were measured based on the functional additives applied. When PEG and GMA were applied to the composites, the water absorption rate increased-including the initial rate-compared to that measured when functional additives were not used. The results also show that PEG has a hydrophilic functional group, which allows it to absorb more water, and GMA acts as a coupling agent between CR and SAP. However, with the introduction of functional additives, the cure rate slowed down and the mechanical properties also decreased.

• 대한치과보철학회지
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• 제55권3호
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• pp.305-310
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• 2017

최근, CAD/CAM 기술이 발전하면서 하이브리드 보철물의 제작에 이용되고 있다. Double scanning technique은 시적용 납의치와 주모형을 스캔 후 중첩하여, 가상 디자인의 현실화와 보철 기공 과정의 간소화를 이루었다. 본 증례에서는 금속 혹은 지르코니아 대신 고성능 중합체인 Polyetherketoneketone (Pekkton, Cendres+$M{\acute{e}}taux$, Biel, Switzerland)를 framework의 재료로 사용했으며, 콤포짓이나 세라믹 혹은 의치용 치아 대신 Polymethyl methacrylate (PMMA) 비니어링 치아(Visio-lign, Bredent, Senden, Germany)를 최종 보철물로 사용하였다. Pekkton과 Visio-lign을 사용한 본 증례에서 만족할만한 치료 결과와 환자의 만족을 얻었으며, 추후 주기적인 유지관리 및 평가가 필요할 것으로 사료된다.

• Korean Chemical Engineering Research
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• 제47권4호
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• pp.476-480
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• 2009

본 연구는 리튬 이차전지용 고분자 전해질 복합재료에 관한 것으로, 고분자는 poly(ethylene oxide)(PEO)와 poly(methyl methacrylate) (PMMA) 블렌드를 사용하고, 용매로는 Ethylene carbonate(EC), 그리고 $LiClO_4$를 리튬염으로 하는 전해질 복합체 필름을 제조하였으며, PMMA의 함유량에 따른 고분자 전해질의 전기화학적 특성을 관찰하였다. 제조된 고분자 전해질의 결정화도와 이온전도도는 시차주사열량계(DSC)와 주파수반응분석기(FRA)로 분석하였다. 그 결과 PMMA의 함량을 증가시킴에 따라서, PEO의 결정 영역이 감소하고 이온전도도가 증가하였다. 또한, PMMA의 함량이 20 wt.% 이상인 경우, 고분자 블렌드필름에서 상분리되는 현상을 관찰하였다. 즉, SEM 분석결과에 의해서, PMMA 주성분 영역과 PEO 주성분 영역의 구분이 가능하였다. 고분자 전해질의 이온전도도는 20 wt.% 첨가한 경우 가장 큰 이온전도도를 가지며, 함유량이 20 wt.% 이상에서는 PMMA 상의 증가로 인해 다소 감소된 이온전도도 변화를 나타내었다.

• The Journal of Advanced Prosthodontics
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• 제6권5호
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• pp.333-345
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• 2014

PURPOSE. Bonding agents (BA) are the crucial weak link of composite restorations. Since the commercial materials' compositions are not disclosed, studies to formulize the optimum ratios of different components are of value. The aim of this study was to find a proper formula of BAs. MATERIALS AND METHODS. This explorative experimental in vitro study was composed of 4 different sets of extensive experiments. A commercial BA and 7 experimental formulas were compared in terms of degree of conversion (5 experimental formulas), shear bond strength, mode of failure, and microleakage (3 experimental formulas). Statistical analyses were performed (${\alpha}$=.05). The DC of selected formula was tested one year later. RESULTS. The two-way ANOVA indicated a significant difference between the shear bond strength (SBS) of two tissues (dentin vs. enamel, P=.0001) in a way that dentinal bonds were weaker. However, there was no difference between the four materials (P=.283). The adhesive mode of failure was predominant in all groups. No differences between the microleakage of the four materials at occlusal (P=.788) or gingival (P=.508) sites were detected (Kruskal-Wallis). The Mann-Whitney U test showed a significant difference between the microleakage of all materials (3 experimental formulas and a commercial material) together at the occlusal site versus the gingival site (P=.041). CONCLUSION. A formula with 62% bisphenol A-glycidyl methacrylate (Bis-GMA), 37% hydroxy ethyl methacrylate (HEMA), 0.3% camphorquinone (CQ), and 0.7% dimethyl-para-toluidine (DMPT) seems a proper formula for mass production. The microleakage and SBS might be respectively higher and lower on dentin compared to enamel.

• Elastomers and Composites
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• 제40권1호
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• pp.59-65
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• 2005

메타크릴산의 아연염인 ZMA를 EPDM고무와 직접 블렌딩하거나 또는 ZnO와 MAA의 형태로 첨가한 후 이들간의 중화반응을 유도하여 고무에 in-situ로 형성시키는 방법을 이용하여 EPDM/ZMA 복합체를 제조하였다. 인장시험, 인열시험, 열노화시험 결과 ZMA의 첨가는 EPDM의 기계적 물성 및 열노화에 대한 안정성을 현저히 향상시킬 수 있음을 알 수 있었다. 또한 ZMA의 첨가는 EPDM고무와 금속과의 접착력을 크게 향상시킬 수 있음을 알 수 있었다. 이러한 기계적물성 및 접착물성의 향상효과는 과량의 ZnO를 사용한 중화반응에 의해 ZMA를 형성시킨 복합체에서 더욱 크게 나타났다. 이는 ZMA의 도입에 의한 이온가교결합의 형성 및 고무매트리스에서의 ZMA 도메인의 분산도와 연관되는 것으로 판단되었다.

• 대한치과보철학회지
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• 제41권4호
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• pp.476-492
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• 2003

Purpose : The purpose of this study was to compare HEMA and TEGDMA as diluents for the composite resin. Material and methods : Eight kinds of experimental light curable composite resins were prepared and used. Concentrations of monomer and filler were same for all experimental composites, except, the diluent's ratios to the monomer. The ratio of diluents to Bis-GMA were 15%, 20%, 25%, and 30%, and two kinds of diluents were used, so total experimental groups were eight including one control group of 25% TEGDMA. Results : Depth of cure, flexural strength, shear bond strength to bovine enamel, shear bond strength to bovine dentin, water absorption and solubility of composites in water were measured. Sample size for each groups were 10. Arithmetic means were used as each groups representative values, and regression test for two diluents and low concentrations, Duncan's multiple range test, and Two-way ANOVA test were done for kinds of diluents and its concentrations at level of 0.05. Conclusion : Following results were obtained ; 1. There were not significant differences in effects of HEMA and TEGDMA to depth of cure, flexural strength of composites and shear bond strength to bovine enamel (p>0.05). 2. Increase of the concentrations of the diluents made the depth of cure (p<0.001) and flexural strength (p<0.05) a little higher. 3. Shear bond strength to dentin was higher on HEMA containing composites than TEGDMA containing composites (p<0.001). 4. Water absorption was higher on HEMA containing composites than TEGDMA containing composites (p<0.01).

• 한국세라믹학회지
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• 제52권5호
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• pp.320-324
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• 2015

Optimization of the fabrication process of NiO-yttrium doped barium zirconate (BZY) composite anode substrates using tape-casting for high performance thin-film protonic ceramic fuel cells (PCFCs) is investigated. The anode substrate is composed of a tens of microns-thick anode functional layer laminated over a porous anode substrate. The macro-pore structure of the anode support is induced by micron-scale polymethyl methacrylate (PMMA) pore formers. Thermal gravity analysis (TGA) and a dilatometer are used to determine the polymeric additive burn-out and sintering temperatures. Crystallinity and microstructure of the tape-cast NiO-BZY anode are analyzed after the sintering.

• Restorative Dentistry and Endodontics
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• 제45권3호
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• pp.32.1-32.12
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• 2020

Objectives: To evaluate the polymerization efficiency of a matrix-modified bulk-fill composite, and compare it to a conventional composite which has a similar filler system. The degree of conversion (DC%) and monomer elution were measured over different storage periods. Additionally, fillers' content was examined. Materials and Methods: Cylindrical specimens were prepared, in bulk and incrementally, from Filtek Bulk Fill (B) and Filtek Supreme XTE (S) composites using a Teflon mold, for each test (n = 6). Using attenuated total reflection method of Fourier transformation infrared spectroscopy, DC% was measured after 24 hours, 7 days, and 30 days. Using high-performance liquid chromatography, elution of hydroxyethyl methacrylate, triethylene glycol dimethacrylate, urethane dimethacrylate, and bisphenol-A glycidyl dimethacrylate was measured after 24 hours, 7 days and 30 days. Filler content was examined by scanning electron microscopy (SEM). Data were analyzed using 2-way mixed-model analysis of variance (α = 0.05). Results: There was no significant difference in DC% over different storage periods between B-bulk and S-incremental. Higher monomer elution was detected significantly from S than B. The elution quantity and rate varied significantly over storage periods and between different monomers. SEM images showed differences in fillers' sizes and agglomeration between both materials. Conclusions: Matrix-modified bulk-fill composites could be packed and cured in bulk with polymerization efficiency similar to conventional composites.