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Effects of silane-modified fillers on properties of dental composite resin

机译:硅烷改性填料对牙科复合树脂性能的影响

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The effect of silanization on the mechanical, chemical, and physical properties of dental composites was investigated. Silica fillers were obtained from colloidal silica solution, Ludox (R) HS40 and they were silanized by using 3methacryloxypropyl trimethoxysilane (MPTMS) in an acidic media. Mineralogical and chemical structures of unsilanized and silanized fillers were determined by using XRD and FTIR analyses. The modification of unsilanized/silanized fillers were investigated by performing XPS and TGA analyses. The morphological evaluations, surface area, and particle size measurements were performed by using SEM, BET, and ZetaSizer, respectively. Eventually, pure and amorphous silica fillers were obtained. Furthermore, the weight percentage of the silane in silica/silane structure was compatible with theoretical values. SEM images, surface area, and particle size measurements showed that agglomeration tendencies of silanized fillers were lower compared to silanized fillers because of the MPTMS addition. Experimental composites (5/10/10/5BisGMA/HEMA/UDMA/TEGDMA resin reinforced with 70 wt% silanized/unsilanized SiO2) were fabricated into 4 mm diameter x 6 mm thick discs for compressive strength (CS), angular flexural strength (AFS), curing depth (CD), and polymerization shrinkage (PS) on a 25 x 2 x 2mm rectangular Teflon mold for flexural strength (FS) and modulus of elasticity (E) tests. The curing depth (CD) and degree of polymerization percentage (DP) of composites were determined. Consequently, results showed that mechanical properties and DP of composite resins can be greatly influenced by silanization as a result of the organic matrix inorganic filler interface bonding formed by silane structures. Despite of these findings, silanization of the SiO2 was not effected DC and PS values. (C) 2017 Elsevier B.V. All rights reserved.
机译:研究了硅烷化对牙科复合材料的机械,化学和物理性质的影响。从胶体二氧化硅溶液中获得二氧化硅填料,通过在酸性介质中使用3甲基丙烯酰氧基丙基三甲氧基硅烷(MPTMS)硅烷化。通过使用XRD和FTIR分析测定未泛化和硅烷化填料的矿物学和化学结构。通过进行XPS和TGA分析研究了不泛化/硅化填料的改变。通过使用SEM,BET和Zetasizer来进行形态学评估,表面积和粒度测量。最终获得纯和无定形二氧化硅填料。此外,二氧化硅/硅烷结构中硅烷的重量百分比与理论值相容。 SEM图像,表面积和粒度测量表明,由于硅烷化填料,硅烷化填料的聚集趋势由于硅烷化填料而添加,因此加入。实验复合材料(用70wt%硅烷化/不粉状的SiO 2增强5 / 10/10 / 5bisgma / hema / udma / tegdma树脂)制成4mm直径×6mm厚的盘,用于压缩强度(Cs),角弯曲强度(AFS ),固化深度(CD),以及25×2×2mm矩形Teflon模具上的聚合收缩(PS),用于弯曲强度(FS)和弹性模量(E)测试。确定了复合材料的固化深度(CD)和聚合百分比(DP)。因此,结果表明,由于通过硅烷结构形成的有机基质无机填充界面粘合,可以通过硅烷化大大影响复合树脂的机械性能和DP。尽管有这些发现,但是SiO2的硅烷化未进行DC和PS值。 (c)2017 Elsevier B.v.保留所有权利。

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