Aydınoğlu Aysu, Yoruç Afife Binnaz Hazar
Department of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Yildiz Technical University, Davutpaşa Cad. No.127, 34210, Esenler, Istanbul, Turkey.
Department of Metallurgical and Materials Engineering, Faculty of Chemical and Metallurgical Engineering, Yildiz Technical University, Davutpaşa Cad. No.127, 34210, Esenler, Istanbul, Turkey.
Mater Sci Eng C Mater Biol Appl. 2017 Oct 1;79:382-389. doi: 10.1016/j.msec.2017.04.151. Epub 2017 Apr 27.
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® HS-40 and they were silanized by using 3-methacryloxypropyl trimethoxysilane (MPTMS) in an acidic media. Mineralogical and chemical structures of unsilanized and silanized fillers were determined by using XRD and FT-IR 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 Zeta-Sizer, 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 70wt% silanized/unsilanized SiO) were fabricated into 4mm diameter×6mm thick discs for compressive strength (CS), angular flexural strength (AFS), curing depth (CD), and polymerization shrinkage (PS) on a 25×2×2mm 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 SiO was not effected DC and PS values.
研究了硅烷化对牙科复合材料力学、化学和物理性能的影响。二氧化硅填料由胶体二氧化硅溶液Ludox® HS - 40制得,并在酸性介质中使用3 - 甲基丙烯酰氧基丙基三甲氧基硅烷(MPTMS)进行硅烷化处理。通过XRD和FT - IR分析确定未硅烷化和硅烷化填料的矿物学和化学结构。通过XPS和TGA分析研究未硅烷化/硅烷化填料的改性情况。分别使用SEM、BET和Zeta粒度分析仪进行形态学评估、表面积和粒度测量。最终,获得了纯净的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符。SEM图像、表面积和粒度测量结果表明,由于添加了MPTMS,硅烷化填料的团聚倾向比未硅烷化填料低。将实验复合材料(由70wt%硅烷化/未硅烷化的SiO增强的5/10/10/5双酚A甘油醚甲基丙烯酸酯/甲基丙烯酸羟乙酯/二甲基丙烯酸脲烷酯/三乙二醇二甲基丙烯酸酯树脂)在25×2×2mm的矩形聚四氟乙烯模具中制成直径4mm×厚度6mm的圆盘,用于抗压强度(CS)、角弯曲强度(AFS)、固化深度(CD)和聚合收缩率(PS)测试,以及在25×2×2mm的矩形聚四氟乙烯模具中制成用于弯曲强度(FS)和弹性模量(E)测试的样品。测定了复合材料的固化深度(CD)和聚合度百分比(DP)。结果表明,由于硅烷结构形成的有机基体 - 无机填料界面结合,硅烷化可极大地影响复合树脂的力学性能和DP。尽管有这些发现,但SiO的硅烷化对DC和PS值没有影响。