• 한국재료학회지
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• 제29권4호
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• pp.221-227
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• 2019

This study examines the role of the nano- and micro-particle ratio in dispersion stability and mechanical properties of composite resins for SLA(stereolithography) 3D printing technology. VTES(vinyltriethoxysilane)-coated $ZrO_2$ ceramic particles with different nano- and micro-particle ratios are prepared by a hydrolysis and condensation reaction and then dispersed in commercial photopolymer (High-temp) based on interpenetrating networks(IPNs). The coating characteristics of VTES-coated $ZrO_2$ particles are observed by FE-TEM and FT-IR. The rheological properties of VTES-coated $ZrO_2/High-temp$ composite solution with different particle ratios are investigated by rheometer, and the dispersion properties of the composite solution are confirmed by relaxation NMR and Turbiscan. The mechanical properties of 3D-printed objects are measured by a tensile test and nanoindenter. To investigate the aggregation and dispersion properties of VTES-coated $ZrO_2$ ceramic particles with different particle ratios, we observe the cross-sectional images of 3D printed objects using FE-SEM. The 3D printed objects of the composite solution with nano-particles of 80 % demonstrate improved mechanical characteristics.

• Restorative Dentistry and Endodontics
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• 제14권1호
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• pp.41-56
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• 1989

The purpose of this study was to examine the effect of temperature dependence of the behavior on the physical properties of posterior composite resins. Three light cure posterior composite resins (Heliomolar, Litefil-P, and P-50) and one chemical cure posterior composite resin (Bisfil-II) were used as experimental materials. Composite resin was placed in a cylindrical brass mold (2.5 mm high and 6.5 mm inside diameter) that was rested on a glass plate. Another flat glass was placed on top of the mold, and the plate was tightly clamped together. After the mold had been filled with the light cure composite material, the top surface was cured for 30 seconds with a light source. Chemical cure resin specimens were made in the same manner as above. Three hundreds and twenty composite resin specimens were constructed from the four composite materials. One hundred and sixty specimens of them were placed in a heater at $50^{\circ}C$, $75^{\circ}C$, $100^{\circ}C$, $125^{\circ}C$, $150^{\circ}C$, $175^{\circ}C$ and $200^{\circ}C$ for 5 minutes or 10 minutes respectively before compressive strengths were measured. Another one hundred and sixty specimens were tested for the diametral tensile strengths in the same way as above. They were randomly divided into eight groups according to the mode of heating methods as follows and stored in distilled water at $37^{\circ}C$ for 24 hours. Group $37^{\circ}C$ - specimens were stored at $37^{\circ}C$ in distilled water for 24 hours. Group $50^{\circ}C$ - specimens were heated at $50^{\circ}C$ after curing. Group $75^{\circ}C$ - specimens were heated at $75^{\circ}C$ after curing. Group $100^{\circ}C$ - specimens were heated at $100^{\circ}C$ after curing. Group $125^{\circ}C$ - specimens were heated at $125^{\circ}C$ after curing. Group $150^{\circ}C$ - specimens were heated at $150^{\circ}C$ after curing. Group $175^{\circ}C$ - specimens were heated at $175^{\circ}C$ after curing. Group $200^{\circ}C$ - specimens were heated at $200^{\circ}C$ after curing. Twenty specimens of each of four composite resins were respectively made by insertion of materials into same mold for examining the dimensional changes between before and after heating. The final eighty specimens were stored in distilled water at $37^{\circ}C$ for 24 hours before testing the dimensional changes. Compressive and diametral tensile strengths were measured crosshead speed 1mm/minute and 500Kg in full scale with a mechanical testing machine (DLC 500 Type, Shimadzu Co., Japan). Dimensional changes were determined by measuring the diametral changes of eighty specimens with micrometer (Mitutoyo Co., Japan). Results were as follows: 1. Diametral tensile strengths of specimens in all groups were increased with time heated compared with control group except for that in group $50^{\circ}C$ and the maximum diametral tensile strength was appeared in the specimen of Litefil-P heated for 10 minutes at $100^{\circ}C$. In heliomolar and P-50, it could be seen in the specimen heated for 10 minutes at $150^{\circ}C$, but in Bisfil-II, it could be found in the specimen heated for 5 minutes at $150^{\circ}C$. 2. Compressive strengths of specimens in all groups was tended to be also increased with time heated but that in group $50^{\circ}C$ and the maximum compressive strengths were showed in the same specimens conditioned as the diametral tensile strengths of four composite materials tested. 3. In Heliomolar, Litefil-P, and Bisfil-II, it was decreased in diameters of resin specimens between before heating and increased in diameters of resin specimens after storing in distilled water, but it was not in P-50. 4. There is little difference in diametral tensile strengths, compressive strengths, and dimensional changes followed by heating the resin specimens for 5 minutes and 10 minutes, but there is no statistical significances.

• 한국복합재료학회:학술대회논문집
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• 한국복합재료학회 2003년도 추계학술발표대회 논문집
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• pp.103-106
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• 2003

In this work the novel potential epoxy resins, were synthesized and acrylated. Their structures were confirmed by means of FTIR, $^1H NMR, and^{13}/C NMR$ spectroscopies. Also, we were to note the effect of W curing on functional group changes of VE/UP blend system after UV curing.

• Restorative Dentistry and Endodontics
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• 제21권1호
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• pp.360-365
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• 1996

The purpose of this study was to evaluate the changes in the degree of conversion on a composite resin surface following heat treatment and mylar strip finishing. The effects of the time interval between the light-curing and heat-curing process were also evaluated. The composite resin surface which had been covered with a coverglass showed a lower conversion rate than the surface from which a layer of $500{\mu}m$ was ground away. The composite resin surface was definitely affected by oxygen during the heat curing process when it had not been insulated. When the composite resins were heat cured after 3 days of storage following the light curing process, the increased in the degree of conversion through heatcuring was limited.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1988년도 전기.전자공학 학술대회 논문집
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• pp.343-345
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• 1988

In this paper the fabrication and application of Composite-Thermistor were studied. Composite-Thermistor specimens were made by conventional process. Some compounds of vanadium oxides and semiconductor oxides as a fillers were used to fabricate Composite-Thermistor, and Epoxy Resins are used as a polymer matrix. The results of resistivity-temperature characteristics were measured in the range from -100 ($^{\circ}C$) to 200($^{\circ}C$). The harder polymer, Eccogel series #1365-80 and Spurr Epoxy are more preferable compared to the Eccogel (1365-45) with some fillers.

• Restorative Dentistry and Endodontics
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• 제13권2호
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• pp.207-220
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• 1988

The purpose of this study was to measure roughness on the polished surfaces of composite resin, and was to observe the polished surfaces under Scanning Electron Microscope. The surface roughness tester (Surfcom 700A Semitsu Profilometer Tokyo. Japan) was used to measure roughness of polished surfaces. In this study, 4 brands of composite resin were examined, Pyrofil bond anterior Bell-Feel anterior Clearfil F II and Microrest A.P. White point, Silicone point, Super snap, and Sof-Lex medium disc as cutting instrument, and celluloid matrix were used. The results obtained were as follows. 1) The celluloid matrix produced the smoothest surfaces. 2) Microrest composite resin had smoother surface than any other composite resins after polishing. 3) The values of surface roughness made by White point, Silicon point and Super snap were similar. 4) The surfaces made by Sof-Lex medium disc was smoother than the surfaces made by any other polishing instruments.

• 구강회복응용과학지
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• 제39권4호
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• pp.195-203
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• 2023

목적: 본 연구는 서로 다른 필러를 가지는 복합레진에서 표면 연마 정도에 따라 수종의 레진 표면 강화제(Surface sealant)를 도포했을 때 복합레진의 거칠기에 미치는 영향에 대해 연구해 보고자 한다. 연구 재료 및 방법: 미세입자형 복합레진(Metafil CX, Sun Medical Co.)과 혼합형 복합레진(Aelite^TM LS posterior, Bisco)을 사용하여 직경 8 mm, 높이 4 mm의 시편을 레진당 60개씩 제작하고, 3개 군으로 나누어 주수 하에 600, 1000, 2000 grit 사포(Tamiya finishing abrasives, Tamiya Inc.)로 연마하였다. 연마된 표면의 표면 조도(Ra)값은 Surface Roughness Tester (SJ-301, Mytutoyo)를 이용해 측정하였으며 연마된 각 시편에 레진 표면 강화제인 BisCover^TM LV (Bisco), Optiguard^® (Kerr), and Seal-n-Shine^TM (Pulpdent)를 각각 제조사의 지시에 따라 도포하였다. 레진 표면 강화제 처리 전과 후에 시편의 표면 조도를 측정하였으며 주사전자현미경(JSM-7500, JEOL)과 원자현미경(MultiMode IV, Veeco Instruments)으로 관찰하였다. 결과: 600 grit 사포로 연마한 후 레진 표면 강화제를 처리한 군은 도포 전보다 더 낮은 표면 조도(Ra)값을 보였으나(P < 0.05), 1000, 2000 grit으로 연마한 군에서는 도포 전 후 간에 통계적으로 유의한 차이를 보이지 않았다. 레진 표면 강화제 제품 간 뚜렷한 거칠기 차이는 나타나지 않았다. SEM과 AFM으로 시편을 관찰 시 마무리와 연마 후 레진 표면에 형성된 미세한 결함이 레진 표면 강화제를 처리한 후 현저히 줄어드는 양상을 보였다. 결론: 본 연구 결과, 마무리와 연마 후 복합레진 표면이 거친 경우에는 레진 표면 강화제의 도포가 미세한 결함을 채워서 거칠기에 영향을 줄 수 있지만 복합레진 표면의 연마 상태가 우수한 경우 레진 표면 강화제의 도포가 거칠기에 크게 영향을 주지 않음을 보여준다.

• Journal of the Korean Wood Science and Technology
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• 제41권1호
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• pp.64-76
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• 2013

이 연구에서는 녹차-목재섬유 복합보드의 강도성능과 기능성을 보강한 건축내장재를 개발하기 위하여, 목재섬유에 녹차와 흑탄, 백탄, 활성탄 등 3종류의 숯을 혼합한 녹차-숯-목재섬유 복합보드를 제작하였고, 구성원료의 종류 및 그 배합비율이 복합보드의 정역학적 성능에 미치는 영향을 조사하였다. 녹차-숯-목재섬유 복합보드의 휨 강도성능은 백탄함유 복합보드에서 평균적으로 가장 높은 값을 나타내었으나, 숯의 종류에 따른 휨 강도성능의 차이는 크지 않았다. 그러나 그 값은 선행연구의 녹차-목재섬유 복합보드보다 현저한 휨 강도성능의 향상을 나타내었고, 녹차와 숯의 배합비율이 증가할수록 휨 강도성능의 감소가 확인되었다. 바인더로 사용된 요소수지의 종류에 따른 차이는 $E_1$급 요소수지를 사용한 복합보드가 $E_0$급 요소수지를 사용한 그것보다 높은 휨 강도성능을 나타냈지만, 양 수지간의 차이는 선행연구의 녹차-목재섬유 복합보드에 비해 현저히 감소하였다. 복합보드의 박리강도는 백탄 $$\geq_-$$ 활성탄 > 흑탄함유 복합보드의 순이었고, 백탄함유 복합보드에서는 목재섬유로만 구성된 대조보드와 거의 비슷한 값을 나타내는 것이 확인되었다.

• 대한치과보존학회:학술대회논문집
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• 대한치과보존학회 2002년도 추계학술대회
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• pp.671-671
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• 2002

No Abstract, See Full Text

• 대한치과의사협회지
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• 제15권12호
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• pp.1009-1012
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• 1977