• Restorative Dentistry and Endodontics
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• 제28권3호
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• pp.209-221
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• 2003

The objectiveness of this study was to evaluate whether low-viscosity composite can bond effectively to dentin surface without bonding resin. The low-viscosity composites being 50wt% filler content were made by the inclusion of bonding resin of two self-etching systems(Cleafil SE Bond, Unifil Bond) varied with contents as 0, 10, 20, 30, 40, 50wt%. Exposed dentin surfaces of extracted 3rd molars are used. Dentin bond strengths were measured. The tests were carried out with a micro-shear device placed testing machine at a CHS of 1mm/min after a low-viscosity composite was filled into an iris cut from micro tygon tubing with internal diameter approximately 0.8mm and height of 1.0mm. 1 Flexural strength and modulus was increased with the addition of bonding resin. 2. Micro-shear bond strength to dentin was improved according to content of bonding resin irrespective of applying or not bonding resin in bonding procedure, and that of Clearfil SE Bond groups was higher than Unifil Bond. 3. There were no significant difference whether use of each bonding resin in bonding procedure for S-40, S-50, U-50(p＞0.05). 4. In SEM examination, resin was well infiltrated into dentin after primed with self-etching primer only for S-50 and U-50 in spite of the formation of thinner hybrid layer. Low viscosity composite including some functional monomer may be used as dentin bonding resin without an intermediary bonding agent. It makes a simplified bonding procedure and foresees the possibility of self-adhesive restorative material.

• Restorative Dentistry and Endodontics
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• 제20권1호
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• pp.97-112
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• 1995

The purpose of this study was to evaluate the effect of wetting condition made by drying time on bonding of resin cement to dentin. Freshly extracted bovine teeth were grinded to expose flat dentin surfaces. After the exposed dentin surfaces were treated with pretreatment agents and water rinse, each wetting condition of dentin surfaces was made according to drying times and methods including slight blow bry for I-second by air syringe, blow dry for 20-second by air syringe, and 12-hour dry in desiccator respectively. and then, previously made composite resin specimens were bonded onto each conditioned dentin surface of the specimen using Panavia-21(Kuraray Co.), Bistite(Tokuso Co.), and Choice(use with All bond-2, Bisco Inc.) resin cement according as manufacturer's instruction. Bonded specimens were stored in $37^{\circ}C$ distilled water for 24 hours, then the tensile bond strength was measured, cohesive failure rate was calculated, and fractured dentin surfaces and acrylic rod sides were examined under scanning electron microscope. The result were as follows ; In the group of bonding with Panavia-21 resin cement, higher tensile bond strength was seen in 12-hour dry group than in I-second and 20-second dry group(p<0.01). In the group of bonding with Bistite resin cement, higher tensile bond strength was seen in 1-second dry group than in 20-second and 12-hour dry group(p<0.01). In the group of bonding with Choice resin cement, no significant differences of bond strength under given drying time were seen. Cohesive failure rates derived from the groups of bonding with Panavia-21 and Choice resin cement were increased with the increase of tensile bond strength in each drying time. On SEM examination of fractured surface, adhesive failure mode with fractured resin tags was mostly seen in wet condition with I-second drying time in the group of bonding with Panavia-21 resin cement, mixed failure mode with shortened and fractured resin tag was seen in the group of bonding with Bistite resin cement, and regardless of drying time, and cohesive-adhesive mixed failure mode with fracture of 'Hollow' typed resin tags was mainly seen in the group of bonding with Choice resin cement.

• 구강회복응용과학지
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• 제30권2호
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• pp.102-111
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• 2014

목적: 본 연구의 목적은 air-blasting particle size를 달리하고 분사 압력과 시간을 통상보다 크게 증가시켜 표면에 큰 손상을 유발한 군을 상대적으로 작은 손상을 유발한 군과 비교하여 파절 저항과 접착 강도 차이를 보이는지 평가하는 데 있다. 연구 재료 및 방법: 지르코니아($LAVA^{TM}$) 디스크 표면에 각각 $30{\mu}m$- particle size (Cojet) 2.8 bar 15초, $110{\mu}m$- (Rocatec) 2.8 bar 15초, $110{\mu}m$- (Rocatec) 3.8 bar 30초로 조건을 달리하여 표면처리 후 각각 이축 굽힘하중 강도 실험과 접착 파절 하중 실험을 실행하였다. 접착은 상아질 유사 베이스에 $200{\mu}m$ 두께의 레진시멘트로 시행하여 인장력을 극대화하였으며 음향방출(AE) 센서로 실패하중을 검출하였다. 결과: 이축 굽힘하중 강도, 접착 파절하중은 세 군간 서로 유의성 있는 차이를 보이지 않았다(P > 0.05). 접착 시편의 균열은 대부분 radial crack이었다. 결론: 정하중 평가의 한계 내에서, air-blasting particle size와 압력에 의한 표면 손상은 크지 않았으며, 접착 파절하중 평가는 표면 손상과 접착 강도를 동시에 평가할 수 있는 방법이라 여겨진다.

• 대한소아치과학회지
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• 제33권3호
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• pp.377-387
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• 2006

본 연구는 자가산부식 접착시스템과 자가산부식 프라이머 접착시스템의 다층적용이 혼성층 및 adhesive layer의 형성 양상, 그리고 전단결합강도에 미치는 영향 등을 비교 평가하기 위하여 시행되었다. 영구 구치 140개의 치아를 근원심으로 분할하여 협면 혹은 설면의 상아질을 이용하였다. 각 접착시스템을 1회, 2회, 3회 도포, 그리고 1회 도포 후 광중합한 후 1회의 추가 도포한 군으로 분류하였다. 전단결합강도와 혼성층 및 adhesive layer 두께를 측정하여 분석한 결과 다음과 같은 결론을 얻었다. 1. 모든 접착제에서 도포횟수가 증가함에 따라 adhesive layer의 두께가 증가하였으며 (p<0.05), Adpor Prompt L-Pop과 Xeno III에서는 자가산부식 프라이머 시스템에서보다 작게 나타났다(p<0.05). 2. Adpor Prompt L-Pop에서 혼성층은 도포횟수에 따라 혼성층의 두께도 증가하였다(p<0.05). 3. Unifill Bond와 Clearfill SE Bond의 전단결합강도는 Scotchbond Multi-Purpose Plus와 Adpor Prompt L-Pop에서보다 높게 나타났으며 (p<0.05), Xeno III와는 유사하였다. 4. Adpor Prompt L-Pop은 접착제의 도포횟수가 증가함에 따라 전단결합강도는 유의하게 증가되었으며(p<0.05), AdheSE에서는 3회 도포한 경우 전단결합강도가 감소하는 경향을 보였다(p>0.05). 5. Adpor Prompt L-Pop과 Xeno III에서 첫 층을 중합한 후 두 번째 층을 추가 도포한 경우 전단결합강도는 감소하였다(p<0.05).

• 대한치과교정학회지
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• 제31권1호
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• pp.137-147
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• 2001

Acidic primer는 하나의 용액으로 conditioning과 priming을 동시에 시행하는 새로운 접착 시스템으로 치질의 손상이 적고 처리 과정이 간단한 특징을 지닌다. 본 실험은 acidic primer를 이용하여 치면처리를 시행한 후 기존의 접착제로 브라켓을 접착할 때 적절한 결합강도를 지니는지 평가하기 위하여 고안되었다. 50개의 사람 소구치를 5개군으로 나누어 4개군은 acidic primer로 법랑질을 처리한 후 Clearfil Liner bond $2^{\circledR}$(1군), Transbond $XT^{\circledR}$(2군), Panavla $21^{\circledR}$(3군), Fuji Ortho $LC^{\circledR}$(4군)로 브라켓을 접착하였고 1개군은 TransHond $XT^{\circledR}$를 통상적인 산부식 방법을 이용하여 접착(5군)한 후 전단 결합 강도를 측정하고 접착파절의 양상을 평가하여 다음과 같은 결론을 얻었다. 1 Acidic primer로 처리한 4개의 군 가운데 광중합형 글래스 아이오노머를 사용한 군(4군)의 전단결합강도($9.72{\pm}3.16MPa$)와 Panavia $21^{\circledR}$을 사용한 군(3군)의 전단 결합 강도($8.69{\pm}2.72MPa$)는 37$\%$ 인산으로 처리한 후 광중합형 레진 (Transbond $XT^{\circledR}$)을 사용한 군(5군)의 전단결합강도($10.48{\pm}2.60MPa$)와 유의성있는 차이를 보이지 않았다 (P>0.05). 2. Acidic primer로 처리한 4개의 군 가운데 광중합형 글래스 아이오노머를 사용한 군(4군)과 Panavia $21^{\circledR}$을 사용한 군(3군)의 전단 결합 강도는 Clearfil Liner bond $2^{\circledR}$를 사용한 군(1군)의 전단 결합 강도($1.09{\pm}0.53MPa$)와 광중합형 레진(Transbond $XT^{\circledR}$)을 사용한 군(2군)의 전단 결합 강도($2.70{\pm}1.46MPa$)에 비해 유의하게 큰 강도를 보였다 (p<0.05). 3. 접착제 잔류지수 측정 결과 4군($2.1{\pm}1.1$)과 5군($2.9{\pm}0.3$)의 경우 1군($0.2{\pm}0.4$), 2군($0.3{\pm}0.9$), 3군($0.2{\pm}0.4$)에 비해 접착제 잔류지수가 유의하게 높았다 (p<0.05). 4. 4군과 5군의 접착제 잔류 지수간에는 유의한 차이가 없었다 (p>0.05). 따라서 acidic primer로 치면을 처리하는 방법은 시용되는 접착제에 따라 기존의 산부식 접 착법과 유사한 결합강도를 얻을 수 있어 교정용 브라켓 접착시 산부식 단계를 생략할 수 있는 가능성을 보여준다.

• Restorative Dentistry and Endodontics
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• 제18권2호
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• pp.423-430
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• 1993

The purpose of this study was to investigate the effect of ferric and ferric ions contained in phosphoric acid solution as a pretreatment solution on bonding of MMA/TBBO resin to dentin. Each of 1 % and 3 % ferric chloride. cupric chloride. cupric sulfate. and cupric nitrate was mixed into 10% phosphoric acid solution and pretreated dentin surface of bovine anterior teeth for 30 seconds followed- by water rinse and dry. Tensile bond strength was determined after bonding of pretreated dentin with MMA/TBBO resin by use of brush-on ;technique and storing for 24 hours in 3it distilled water. The amount of cupric ions adsorbed on pretreated dentin surface was detected by Wave-Dispersion X-ray microanalyzer for different groups of each pretreatment solution containing cupric salts. The pretreatment with cupric ions contained in 10% phosphoric acid solution was effective to increase bonding strength of MMA/TBBO resin to dentin but not in case of ferric ions. The pretreatment with 3 % cupric chloride and cupric nitrate both enhanced significant increase in bonding strength compared to the control group of 10% phosphoric acid solution(p<0.05). Cupric ions measured in pretreated dentin surface was higher in 3 % cupric chloride group than in 1% cupric chloride group, but couldn't find distinct relationship from the results of this experiment between the amount of adsorbed cupric ions according to the kind of cupric salts and the bonding strength value.

• 대한치과기공학회지
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• 제39권3호
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• pp.153-159
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• 2017

Purpose: In this study, a corresponding porcelain coating material was applied to dental Co-Cr metal among PFM. Methods: The bonding strength of the fired specimens was measured by a three-point flexural rigidity test. SEM/EDS was used to observe the surface component of specimens. Results: First, All groups were higher than the minimum bonding strength of 25 MPa specified in ISO 9693 for dental metal-ceramics specimens. Second, The bonding strength of control group(WO) is 44.64 MPa. Experimental group DM was 35.45 MPa and DP was 31.82 MPa(P<0.05). Tukey's HSD tests results have shown that the bonding strength in control group(WO) is higher than that of experimental group(DM, DP). Third, In the case of metal - porcelain bonding strength, the application of opaque porcelain and firing were higher than those of the group treated with degassing process. Conclusion: The bonding strength was higher when the powder opaque porcelain was applied than the paste opaque porcelain.

• Bulletin of the Korean Chemical Society
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• 제24권3호
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• pp.325-333
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• 2003

An analysis of the electronic structure and bonding in the ternary silicide YNiSi₃is made, using extended Huckel tight-binding calculations. The YNiSi₃structure consists of Ni-capped Si₂dimer layers and Si zigzag chains. Significant bonding interactions are present between the silicon atoms in the structure. The oxidation state formalism of $(Y^{3+})(Ni^0)(Si^3)^{3-}$ for YNiSi₃constitutes a good starting point to describe its electronic structure. Si atoms receive electrons from the most electropositive Y in YNiSi₃, and Ni 3d and Si 3p states dominate below the Fermi level. There is an interesting electron balance between the two Si and Ni sublattices. Since the ${\pi}^*$ orbitals in the Si chain and the Ni d and s block levels are almost completely occupied, the charge balance for YNiSi₃can be rewritten as $(Y^{3+})(Ni^{2-})(Si^{2-})(Si-Si)^+$, making the Si₂layers oxidized. These results suggest that the Si zigzag chain contains single bonds and the Si₂double layer possesses single bonds within a dimer with a partial double bond character. Strong Si-Si and Ni-Si bonding interactions are important for giving stability to the structure, while essentially no metal-metal bonding exists at all. The 2D metallic behavior of this compound is due to the Si-Si interaction leading to dispersion of the several Si₂π bands crossing the Fermi level in the plane perpendicular to the crystallographic b axis.

• Restorative Dentistry and Endodontics
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• 제19권1호
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• pp.180-193
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• 1994

The purpose of this study was to observe the sealing ability and durability of All-Bond 2, Gluma Bonding System, Scotch bond 2 and Superbond D-liner which are dentin bonding agents used as desensitizing agents. The durability of the sealing ability of the materials were compared after 0, 140, 420, 840 tooth brushing strokes. 120 extracted teeth were divided into 5 groups and the agents were applied to the exposed dentin. No agents was applied on group I, the control group. Each specimen went through thermocycling from $5^{\circ}$ to $55^{\circ}C$, 200 times. Each group was devide into 4 subgroups and artificial tooth brushing strokes were done for 0, 140, 420, 840 times. Finally the specimens were stored in 0.5 % methylene blue solution for 24 hours in a incubator set at $37^{\circ}C$. The tooth were sectioned perpendicular to the long axis and the dye penetration ratio to the pulp was measured. The following results were obtained. 1. All four dentin bonding agents initially showed excellent sealing ability. 2. All-bond 2, Gluma Bonding System and Superbond D-liner showed durability of dentinal tubule sealing effect after 840 strokes(6-week) artificial tooth brushing. 3. Scotchbond 2 showed a significant decrease in sealing ability after 420 strokes(3-week) artificial tooth brushing. (P<0.05).

• 한국세라믹학회지
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• 제31권10호
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• pp.1231-1239
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• 1994

In this study, gel powder which had relatively high hydration reactivity in CaO and P2O5 rich composition of CaO-P2O5-SiO2-H2O system was prepared by sol-gel process and its hydrated specimen was manufactured. The it was investigated to appropriate calcination temperature in sol-gel process which hydrated specimen of gel powder have proven to strength and the effect of factors influenced strength in hydration process. The major product of before and after hydration reaction was hydroxyapatite, and crystalline phase of C-S-H was already formed during gelation process. After hydration reaction of pressed specimen, crystalline phase of C-S-P-H was formed. It was hydrated product of silicocarnotite (5CaO.P2O5.SiO2). Gel phases of C-S-H and C-S-P-H occured as a result of partial substitution of amorphous silica by P2O5 was formed. The strength of hydrated hardened body is developed by strong bonding and bridging between the gel phases of C-S-H or C-S-P-H and the crystalline products such as hydroxyapatite, Ca(OH)2 C-S-H and C-S-P-H. In addition, the ultrafine gel powder have an great effect on increase of hydration reaction.