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首页> 外文期刊>The Journal of Adhesion >Comparison of Physicochemical Surface Conditioning Methods for Adhesion of bis-GMA Resin Cement to Particulate Filler Composite and Surface Characterization
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Comparison of Physicochemical Surface Conditioning Methods for Adhesion of bis-GMA Resin Cement to Particulate Filler Composite and Surface Characterization

机译:bis-GMA树脂与颗粒填料复合物粘合的理化表面调节方法的比较和表面表征

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This study compared the effect of physicochemical surface conditioning methods on the adhesion of bis-GMA-based resin cement to particulate filler composite (PFC) used for indirect dental restorations. PFC blocks (N (block)=54, n (block)=9 per group) were polymerized and randomly subjected to one of the following surface conditioning methods: a) No conditioning (Control-C), b) Hydrofluoric acid (HF)etching for 60s (AE60), c) HF for 90s (AE90), d) HF for 120s (AE120), e) HF for 180s (AE180), and f) air-abrasion with 30 mu m silica-coated alumina particles (AB). The conditioned surfaces were silanized with an MPS silane, and an adhesive resin was applied. Resin composite blocks were bonded to PFC using resin cement and photo-polymerized. PFC-cement-resin composite blocks were cut under coolant water to obtain bar specimens (1mmx0.8mm). Microtensile bond strength test (mu TBS)was performed in a universal testing machine (1mm/min). After debonding, failure modes were classified using stereomicroscopy. Surface characterization was performed on a set of separate specimen surfaces using Scanning Electron Microscopy (SEM), X-Ray Dispersive Spectroscopy (XDS), X-Ray Photoelectron Spectroscopy (XPS), and Fourier Transform-Raman Spectroscopy (FT-RS). Mean mu TBS (MPa) of C (35.6 +/- 4.9) was significantly lower than those of other groups (40.2 +/- 5.6-47.4 +/- 6.1) (p<0.05). The highest mu TBS was obtained in Group AB (47.4 +/- 6.1). Prolonged duration of HF etching increased the results (AE180: 41.9 +/- 7), but was not significantly different than that of AB (p>0.05). Failure types were predominantly cohesive in PFC (34 out of 54) followed by cohesive failure in the cement (16 out of 54). Degree of conversion (DC) of the PFC was 63 +/- 10%. SEM analysis showed increased irregularities on PFC surfaces with the increased etching time. Chemical surface analyses with XPS and FT-RS indicated 11-70% silane on the PFC surfaces that contributed to improved bond strength compared to Group C that presented 5% silane, which seemed to be a threshold. Group AB displayed 83% SiO2 and 17% silane on the surfaces.
机译:这项研究比较了理化表面调节方法对bis-GMA基树脂胶粘剂与用于间接牙齿修复的颗粒填料复合物(PFC)的粘附力的影响。聚合PFC嵌段(每组N(嵌段)= 54,n(嵌段)= 9)并随机进行以下一种表面调节方法:a)无调节(对照C),b)氢氟酸(HF)蚀刻60秒(AE60),c)HF持续90s(AE90),d)HF持续120s(AE120),e)HF持续180s(AE180),以及f)用30μm二氧化硅涂覆的氧化铝颗粒进行空气磨蚀( AB)。用MPS硅烷对经调理的表面进行硅烷化,并施加粘合剂树脂。使用树脂水泥将树脂复合块粘结到PFC上并进行光聚合。将PFC-水泥-树脂复合块在冷却水下切割,以获得条形试样(1mmx0.8mm)。在万能试验机(1mm / min)中进行了微拉伸粘合强度试验(μTBS)。脱胶后,使用立体显微镜对失效模式进行分类。使用扫描电子显微镜(SEM),X射线色散光谱(XDS),X射线光电子光谱(XPS)和傅里叶变换拉曼光谱(FT-RS)在一组单独的样品表面上进行表面表征。 C的平均mu TBS(MPa)(35.6 +/- 4.9)显着低于其他组(40.2 +/- 5.6-47.4 +/- 6.1)(p <0.05)。在AB组中获得最高的mu TBS(47.4 +/- 6.1)。延长HF蚀刻的持续时间可提高结果(AE180:41.9 +/- 7),但与AB的差异无统计学意义(p> 0.05)。在PFC中,破坏类型主要为内聚性(54个中的34个),接着在水泥中发生内聚性破坏(54个中的16个)。 PFC的转化度(DC)为63 +/- 10%。 SEM分析显示,随着蚀刻时间的增加,PFC表面的不规则性增加。用XPS和FT-RS进行的化学表面分析表明,与提供5%硅烷(看来是一个阈值)的C组相比,PFC表面上的11-70%硅烷有助于提高粘结强度。 AB组在表面上显示83%的SiO2和17%的硅烷。

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