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Evaluation of resin adhesion to zirconia ceramic using some organosilanes

机译:使用某些有机硅烷评估树脂对氧化锆陶瓷的附着力

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Objectives. This study evaluated and compared the effect of three trialkoxysilane coupling agents on the bond strength of a Bis-GMA-based unfilled resin and a dimethacrylate-based resin composite luting cement to a zirconia ceramics (Procera~® AllZircon, Nobel Biocare, Goeteborg, Sweden). Methods. Six square-shaped zirconia specimens were used for each test group, a total of 72 specimens. The specimens in each group were all assigned to air-borne alumina particle abrasion followed by tribochemical silica-coating and silanization with 1 vol% solutions of 3-methacryloyloxypropyltrimethoxysilane, 3-acryloyloxypropyltrimethoxysilane, or 3-isocyanatopropyltriethoxysilane in an ethanol-water mixture. The sample stubs were made of a Bis-GMA/MMA/DMAEMA resin or a commercial resin composite luting cement (RelyX™ ARC, 3M ESPE, Seefeld, Germany). They were bonded to the conditioned and silanized silica-coated zirconia specimens using polyethylene molds. All specimens were tested at dry and thermo-cycled (6000, 5-55 ℃, 30 s) conditions. The shear bond strength of resin stubs to zirconia was measured in a universal testing machine (cross-head speed 1 mm/min). Results. In dry conditions, the highest shear bond strength was 9.7 MPa (S.D. 3.3MPa), and for thermo-cycled samples 7.4MPa (S.D. 2.4MPa) was obtained with RelyX™ ARC cement with 3-methacryloyloxypropyltrimethoxysilane. In general, thermo-cycling decreased the bond strengths significantly for the Bis-GMA resin (ANOVA, p < 0.005). The resin, cement and silanes differed significantly silanes (ANOVA, p < 0.005). All samples silanized with 3-isocyanatopropyltriethoxysilane de-bonded during thermo-cycling. De-bondingwas dom-inantly due to adhesive failure. Significance. Bonding of the experimental resin and commercial cement to silica-coated zirconia is effective with 3-methacryloyloxypropyltrimethoxysilane or 3-methacryloyloxypropyltrimethoxysilane, but not with 3-isocyanatopropyltriethoxysilane.
机译:目标。这项研究评估并比较了三种三烷氧基硅烷偶联剂对Bis-GMA基未填充树脂和二甲基丙烯酸酯基树脂复合胶泥与氧化锆陶瓷的粘结强度的影响(Procera〜AllZircon,Nobel Biocare,Goeteborg,Sweden )。方法。每个测试组使用六个方形氧化锆样品,总共72个样品。每组中的样品都被分配到空气传播的氧化铝颗粒上,然后进行摩擦化学二氧化硅涂层和硅烷化,并在乙醇-水混合物中用1体积%的3-甲基丙烯酰氧基丙基三甲氧基硅烷,3-丙烯酰氧基丙基三甲氧基硅烷或3-异氰基丙基丙基三乙氧基硅烷进行溶液硅烷化。样品桩由Bis-GMA / MMA / DMAEMA树脂或商用树脂复合型胶结水泥(RelyX™ARC,3M ESPE,Seefeld,德国)制成。使用聚乙烯模具将它们粘结到经过条件处理和硅烷化的二氧化硅涂层氧化锆样品上。所有样品均在干燥和热循环(6000、5-55℃,30 s)条件下进行测试。用万能试验机(十字头速度1mm / min)测量树脂桩对氧化锆的剪切粘合强度。结果。在干燥条件下,最高剪切粘结强度为9.7 MPa(S.D. 3.3MPa),对于热循环样品,使用具有3-甲基丙烯酰氧基丙基三甲氧基硅烷的RelyX™ARC水泥可获得7.4 MPa(S.D. 2.4MPa)。通常,热循环显着降低了Bis-GMA树脂的粘结强度(方差分析,p <0.005)。树脂,水泥和硅烷与硅烷明显不同(ANOVA,p <0.005)。在热循环过程中,所有被3-异氰酸根合丙基三乙氧基硅烷硅烷化的样品均会脱键。脱胶主要是由于粘合失败。意义。用3-甲基丙烯酰氧基丙基三甲氧基硅烷或3-甲基丙烯酰氧基丙基三甲氧基硅烷将实验树脂和市售水泥粘结到二氧化硅涂覆的氧化锆上是有效的,但是对于3-异氰酸根合丙基三乙氧基硅烷则无效。

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