• 접착 및 계면
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• 제15권3호
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• pp.100-108
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• 2014

본 연구에서는 비스페놀 A 에폭시 수지/경화제(YD-128/DDM) 조성물의 비율을 조절하여 $170^{\circ}C$의 경화온도에서 접착성능 최적화 조성비를 얻기 위한 실험을 진행하였다. DSC, TGA, DMA, TMA 열분석 장비를 사용하여 YD-128/DDM 혼합물의 당량비 변화가 경화물의 열적 특성에 미치는 영향에 대하여 조사하였으며, 조성물의 경화시간은 YD-128/DDM (1 : 1.1) 조성물을 동적 DSC를 이용하여 측정된 시간당 누적 발열량을 총 발열량으로 나누어 계산한 전환율을 토대로 결정하였다. TGA를 이용한 분해 활성화 에너지 분석에서는 경화물의 DDM 당량비가 증가할수록 열안정성과 열분해 활성화 에너지가 높게 나타났고, DMA와 TMA를 이용한 경화물의 열적 특성 조사 결과에서는 당량비 1 : 1에서 다른 당량비 조건에 비해 우수한 탄성률 및 열팽창성이 관찰되었다. 또한 각기 다른 당량비의 조성물을 $170^{\circ}C$에서 경화하여 중첩 전단 강도를 측정하였다.

• 접착 및 계면
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• 제12권3호
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• pp.88-93
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• 2011

페놀수지에 함침된 탄소나노튜브 (CNT)의 최적 분산제조공정은 전기저항 측정으로 구해졌으며, 플라즈마 처리된 탄소섬유와 CNT-페놀수지 나노복합재료간의 계면특성이 전기-미세역학시험법에 의해 연구되었다. 탄소섬유의 젖음성은 플라즈마 처리 후에 현격하게 증가되었다. 탄소섬유와 CNT-페놀수지 나노복합재료의 표면에너지는 Wilhelmy 플레이트 시험법으로 측정되었다. 탄소섬유 표면의 활성화로 인하여 플라즈마 처리 후 전진 접촉각은 $65^{\circ}$에서 $28^{\circ}$로 감소되었다. 이는 정적 접촉각과 상호 일치함을 보여 주었다. 플라즈마 처리된 탄소섬유와 CNT-페놀수지 나노복합재료간의 접착일은 플라즈마 처리전보다 증가하였다. 또한, 계면전단강도와 겉보기 강성도 탄소섬유에 대한 플라즈마 처리로 증가하였다.

• 대한소아치과학회지
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• 제36권3호
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• pp.427-432
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• 2009

본 연구의 목적은 시중에 유통되고 있는 밴드 시멘트들을 종류별로 이용하여 교정용 밴드의 결합강도를 비교하고, 각 시멘트의 파절 양상을 비교하여 교정용 밴드에 대한 사용지침을 마련하는데 도움이 되고자 하였다. 100개의 발거된 인간의 제 3대구치를 이용해 실험군은 총 5개의 군으로 하였으며, 각 군당 시편수가 20개가 되도록 임의적으로 분류하였다. 실험에 사용한 밴드 시멘트는 다음과 같다; Ormco gold, Ultra $Band-Lok^{TM}$, Fuji $Ortho^{TM}$ LC, 3M $Unitek^{TM}$ Multi-Cure Glass Ionomer, $Ketac-Cem^{TM}$. Universal testing machine(Instron Corp., Canton, MA, USA)를 사용하여 최대하중값을 측정하였고, 전단결합강도 값을 계산하였다. 밴드가 탈락한 후, 탈락 부위를 평가하여 법랑질과 시멘트, 시멘트와 밴드 사이로 구분하였다. 밴드의 전단강도는 One-way ANOVA를 이용하여 통계처리 하였으며 Tukey test를 이용하여 검정하였다. 또한 탈락 부위는 Chi-squre analysis를 이용하여 통계 처리하였고, Fisher's exact test로 군간 유의성을 검정하였다. 실험 결과 평균 파절 강도는 Ormco군이 가장 높았고(2.44${\pm}$0.57), Fuji $Ortho^{TM}$군(2.24${\pm}$0.50), $Ketac-Cem^{TM}$군(2.10${\pm}$0.57), 3M $Unitek^{TM}$군(1.82${\pm}$0.43), $Band-Lok^{TM}$군(1.73${\pm}$0.28) 순이었으며, Ormco군은 $Band-Lok^{TM}$군과 3M $Unitek^{TM}$군, Fuji $Ortho^{TM}$군은 $Band-Lok^{TM}$군과만 통계적으로 유의할만한 차이를 보였다(p<0.05). 파절 양상에서 Ormco군과 $Band-Lok^{TM}$군은 서로뿐만 아니라 다른 군과 유의할만한 차이를 보였으며, Fuji $Ortho^{TM}$, 3M $Unitek^{TM}$, $Ketac-Cem^{TM}$ 군 간에는 유의한 차이가 없었다.

• Elastomers and Composites
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• 제45권3호
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• pp.199-205
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• 2010

실내 건축내장재로 medium density fiberboard (MDF)는 널리 사용되는 재료이지만, MDF 합판과 표면재의 바인더로 사용되는 포름알데히드 수지의 유리 포름알데히드와 휘발성 유기화합물의 방산 문제점이 있다. 이를 해결하기위해 본 연구에서는 포름알데히드 흡착성능이 있는 축합형 탄닌을 활용하여 표면재에 적용 하였다. 표면재에 사용되는 수지는 멜라민-포름알데히드 수지와 축합형 탄닌을 사용하여 합성하였으며 반응여부는 FT-IR 스펙트럼으로 확인하였다. 또한 전단응력, 충격강도, 테이프에 의한 접착력 실험, 연필경도, 광택도 그리고 접촉각 등과 같은 표면물성을 측정하였고 미반응 포름알데히드를 분석하기 위하여 유리 포름알데히드 분석법과 소형챔버법이 이용되었다. 결과에 따르면 전단응력과 충격강도는 축합형 탄닌의 함유량이 10 wt.% 일 때 가장 우수한 접착물성을 나타내었지만, 연필경도와 광택도의 경우에는 축합형 탄닌의 함유량이 20 wt.% 일 때 최적의 물성을 발현하였다. 또한 포름알데히드 방산량은 59 ${\mu}g/m^2{\cdot}h$ 로 축합형 탄닌의 첨가에 의해 포름알데히드 방산량을 약 3배 정도 감소 시킬 수 있었다.

• Restorative Dentistry and Endodontics
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• 제24권2호
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• pp.381-391
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• 1999

A new 5th generation adhesive system(ONE-STEP) has been supplied which operators can apply to conditioned tooth surfaces by one simplified step. The purpose of this study was to determine whether different methods of adhesive application and various air drying duration after applying adhesive affect the shear bond strength of composite resin to dentin, and to evaluate the adhesive pattern of composite resin and dentin under SEM. Seventy-seven extracted human molar teeth were cleaned and mounted in palstic test tubes. The occlusal dentin surfaces were exposed with Diamond Wheel Saw and smoothed with Lapping and Polishing Machine (South Bay Technology Co., U.S.A.). Teeth were randomly divided into 7 groups (n=11), In experimental A group, adhesive was applied to dentin with agitation for 20 sec. In experimental N-A group, adhesive were continuously applied to dentin for 20 sec. Also control and experimental 1, 2, 3, 4 groups were dried for 10, 0, 5, 20, 30 seconds after applying adhesive, respectively, Adhesives were light cured for 10 sec. A gelatin capsule 5mm in diameter was filled with Aelitefil$^{TM}$ composite resin, placed on the treated dentin surface and light cured for 40 see, from three sides, All specimens were stored in distilled water at room temperature for 24 hours. The shear bond strengths were measured using a universal testing machine(AGS-1000 4D, Japan) at a crosshead speed of 5mm/min. An one-way ANOVA and LSD test were used for statistical analysis of the data. For SEM evaluation, seven specimens were made and sectioned. Representive postfracture and seven specimens were mounted on brass stubs, sputter-coated with gold and observed under SEM. The results were as follows : 1. The shear bond strength of experimental A group which adhesive were applied to dentin with agitation was higher than that of experimental N-A group (continuous application), and there was significant difference between two groups (p<0.01). 2. The interface between composite and dentin according to different application methods showed close adaptation in experimental A group and showed tinny gap in experimental N-A group. 3. The shear bond strength accoding to various air drying duration was the lowest value(7.57${\pm}$2.60 MPa) in experimental 1 group, so there was significant difference between experimental 1 group and other four groups (p<0.05). But there was no significant difference of shear bond strength between four groups (p>0.05). 4. The interface between composite and dentin according to various air drying duration showed close adaptation in control group and tinny gap in experimental 3 and 4 groups. But experimental 1 and 2 groups showed $30{\mu}$ and 6 - $10{\mu}m$ thick gaps, respectively.

• 마이크로전자및패키징학회지
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• 제22권1호
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• pp.69-74
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• 2015

첨단 전자기기에 사용되는 전자부품의 크기와 접속피치가 감소하면서 리플로우 공정 후 플럭스 잔사의 세정이 어려워짐에 따라 무세정 솔더 페이스트에 대한 요구가 증가하고 있다. 본 연구에서는 SAC305 솔더분말과 에폭시 레진을 주성분으로 하는 경화성 플럭스를 혼합하여 제조한 에폭시 경화형 솔더 페이스트에 대하여 리플로우 공정성, 플럭스 잔사의 부식성, 솔더볼 및 보드레벨 BGA 패키지 솔더 접합부의 기계적 거동을 기존 로진계 솔더 페이스트와 비교하여 평가하였다. 에폭시 경화형 솔더 페이스트는 솔더 접합부 주변에 경화물 필렛을 형성한 것으로 보아 플럭싱 작용에 의해 솔더 접합부가 형성된 이후에 경화반응이 진행되는 것을 확인할 수 있었으며, 동판에 대한 젖음성 시험을 통해 기존상용 솔더 페이스트 정도의 납퍼짐성을 갖는 것을 알 수 있었다. 리플로우 후 동판에 대한 고온 고습 시험을 통해 에폭시 경화형 솔더 페이스트는 동판 부식을 전혀 발생시키지 않는 것으로 나타났는데, 이는 FT-IR 분석결과 에폭시 경화반응을 통해 단단히 고정된 결과로 생각되었다. 볼전단, 볼당김 및 다이전단 시험 결과, 솔더 접합부 주변에 형성된 경화물 필렛은 솔더 표면과 접착본딩을 형성하며, 다이전단강도를 15~40% 정도 향상시키는 것으로 보아 에폭시 경화형 솔더 페이스트는 플럭스 잔사 세정공정의 생략과 함께 솔더 접합부 보강효과를 통해 패키지 신뢰성 향상에도 기여할 수 있을 것으로 생각되었다.

• 대한치과교정학회지
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• 제22권2호
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• pp.449-474
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• 1992

The purpose of this study was to evaluate the in vitro shear bond strengths to enamel and the failure sites of three ceramic brackets and one metal bracket in combination with light cured orthodontic adhesive. The brackets were divided into four groups. Each ceramic bracket group had different bonding mechanisms with adhesive. Group A; metal bracket with foil-mesh base (control group) Group B; ceramic bracket with micromechanical retention Group C; ceramic bracket with chemical bonding Group D; ceramic bracket with mechanical retention and chemical bonding. Forty extracted human lower first premolars were prepared for bonding and 10 brackets for each group were bonded to prepared enamel surfaces with $Transbond^{\circledR}$ light cured ortho dontic adhesive. Twenty four hours after bonding, the Instron universal testing machine was used to test the shear bond strength of brackets to enamel. After debonding, brackets and enamel surfaces were examined under stereoscopic microscope to determine the failure sites, Statistical analysis of the data was carried out with ANOVA test and $Scheff\acute{e}$ test using SPSS PC+. The results were as follows. 1 . There were statistically significant differences in mean shear bond strengths of three ceramic bracket groups (p < 0.05). Shear bond strengths of group C and D were significantly higher than that of group B and shear bond strength of group C was significantly higher than that of group D. 2. Group C and D both had significantly higher shear bond strengths than metal bracket (group A), but there were no significant differences in shear bond strengths between group A and B (p < 0.05). 3. The failure sites of four bracket groups were also different. Group C and D failed primarily at enamel-adhesive interface, but group A and B failed primarily at bracket base-adhesive interface. 4. Among all ceramic bracket groups, group B was very similar to metal bracket in the aspect of shear bond strength and failure site.

• Restorative Dentistry and Endodontics
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• 제24권1호
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• pp.26-39
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• 1999

Bis-GMA, the representative monomer of bonding resin, contributes to the rigidity of bonding layer. Hydrophilic monomer contributes to the permeability into dentin substrates while weaken the bonding layer due to its small molecular weight. The degree of conversion also contributes to the ultimate strength of the bonding layer. This study was performed for the correlation analysis of monomer ratio and dentin bonding strength via degree of conversion. 7 experimental bonding resins were prepared with Bis-GMA, ratio from 20% to 80% by 10% increment, and hydrophilic HEMA monomer. Their degree of conversion and shear bond strength to dentin were compared with Scotchbond Multi-Purpose adhesive, and the fractured surfaces were examined microscopically. The results were as follows; 1. The degree of conversion increased when, the ratio of Bis-GMA increased from 20% to 70%, whereas it decreased when the ratio of Bis-GMA was 80%. 2. Shear bond strengths of the experimental bonding resins of 80%, 70%, 60% ratio of Bis-GMA were significantly higher than those of the experimental bonding resin of 50% ratio of Bis-GMA and Scotchbond Multi-Purpose adhesive. Lower shear bond strengths were obtained with the experimental bonding resins of 40%, 30%, 20% ratio of Bis-GMA (p<0.05). 3. Adhesive fractures were associated with the bonding resins of the lower bond strength, while cohesive fractures within the bonding resin layer were associated with the bonding resins of higher bond strength. Bonding resins with shear bond strength higher than 18MPa showed some cohesive fractures within the composite resin or within the dentin. 4. Correlations between Bis-GMA ratio and the degree of conversion (r=0.826), between Bis-GMA ratio and shear bond strength (r=0.853), and between the degree of conversion and shear bond strength (r=0.786) were significant (p<0.05).

• 대한치과교정학회지
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• 제24권4호
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• pp.957-967
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• 1994

The purpose of this study was to evaluate the effects of different bases of ceramic brackets on shear bond strength and to observe failure patterns of bracket bondings. Lower bicuspid brackets whose bases designed for the macromechanical and silane treated chemical bonding those for silane treated chemical bonding, those for micromechanical bonding, and those for macromechanical bonding were tested as experimental groups, and foil mesh-backed metal brackets as a control group. All the brackets were bonded with $Mono-Lok\;2^{(TM)}$ on the labial surface of extracted human lower bicuspids after etching the enamel with $38\%$ phosphoric acid solution for 60 seconds. The shear bond strengths were measured on the universal test machine after 24 hours passed in the $37^{\circ}C$ water bath. The gathered data were evaluated and tested by ANOVA and Duncan's multiple range test, and those results were as follows. The shear bond strengths of brackets for macromechanical and chemical bonding, those for chemical bonding, and those for micromechanical bonding were not different (p>0.05), but showed statistically higher than those of metal bracket and those of ceramic bracket for micromechanical bonding(p<0.05). The shear bond strengths of ceramic bracket for micromechanical bonding showed statistically lower than those of metal bracket(p<0.05). The enamel fractures and/or ceramic bracket fractures were observed in the cases of higher bond strength than that of metal bracket. These results supported that silane treated base of ceramic bracket show higher shear bond strength than that of metal bracket, and suggested that micromechanical form of ceramic bracket bases show higher shear bond strength than that of macromechanical form.

• 대한치과보철학회지
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• 제33권4호
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• pp.662-684
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• 1995

The purpose of this study was to evaluate the shear bond strength between various resin-bonded retainers and enamel according to the adhesive resins and retention types and observe the bond filure modes with scanning electron microscope(SEM). For this purpose, the followin eight sub-groups were tested in shear bond strength : 1) electrochemically etched group(Verabond) using Panavia EX and Superbond C&B 2) tin-plated group(PG-S) using Panavia EX and Superbond C&B 3) salt-treated group(Verabond) using Panavia EX and Superbond C&B 4) meshtreated group(Verabond) using Panavia EX and Superbond C&B. Thermocycling test was conducted on the condition of 15 second dwell time each in $5^{\circ}C$ and $55^{\circ}C$bath. Shear bond strength was measured by Instron Universal Testing Machine(medel 1125). The obtained results were as follows : 1. After thermocycling, the shear bond strengths of tin-plated group and electrochemically etched group were significantly greater than those of salt-treated group and mesh-treated group. And the shear bond strength of Panavia EX was greater than that of Superbond C&B with salt-treated group and tin-plated group(p<0.05). 2. Before thermocycling, electrochemically etched group using Superbond C&B produced the greatest shear bond strength(p<0.01). 3. The shear bond strength of electrochemically etched group using Superbond C&B was significantly decreased after thermocycling(p<0.01). 4. In observation of bond failure modes before thermocycling, Panavia EX highly exhibited enamel fracture. Tin-plated group using Superbond C&B adhesive failure between metal and resin and electrochemically etched group using Superbond C&B exhibited adhesive failure between enamel and rdsin. 5. In observation of failure modes after thermocycling, Panavia EX exhibited cohesive failure and Superbond C&B exhibited adhesive failure between resin and metal.