Luo J, Lannutti J J, Seghi R R
Department of Materials Science and Engineering, Ohio State University, Columbus 43210-1241, USA.
Dent Mater. 1998 Jan;14(1):29-36. doi: 10.1016/s0109-5641(98)00006-2.
This laboratory study was designed to investigate the effect of controlled nanoporosity on the wear resistance of polymeric composites reinforced with silica gel powders and to determine the mechanisms controlling the abrasive wear properties of these unique nanostructured materials.
Silica gels were prepared by hydrolysis and condensation of tetraethylorthosilicate (TEOS) using four different catalysts to modify the porous structure of the resulting polysilicate silanation, an organic monomer (TEGDMA) containing various initiators was introduced into the gel powders to form a paste. The various pastes were then polymerized inside a glass mold. A pin-on-disk apparatus was then used to record the specimen length and number of revolutions. Abrasive wear rates were determined by regression analysis and statistical differences were determined by analysis of variance and multiple comparisons. BET was used to characterize the filler pore structure and scanning electron microscopy was used used to visually examine the abraded surfaces.
Significant differences (p < 0.05) in the wear rates of the experimental composites were noted. Within the range of filler porosities examined, wear resistance was found to be linearly dependent (R2 = 0.983) on filler pore volume. The wear rates decreased with increasing filler porosity. HCl-catalyzed gels having low porosity produced composites having relatively limited abrasion resistance. In contrast, high porosity HF-catalyzed gels produced more wear-resistant composites. The abrasive wear resistance of these nanocomposites was not significantly affected by the level of silane coupling used in these experiments. SEM evaluation suggested that better wear resistance was associated with fine-scale plastic deformation of the wear surface and the absence of filler particle pullout.
Porous particles prepared via sol-gel show some promise as fillers that improve the wear resistance of photopolymerized resins. The wear resistance of the fillers appears to be directly related to nanoporous structure of the gel particles. Unlike conventional dental composites, these materials rely primarily on nanomechanical coupling for improved wear resistance. This new principle should benefit subsequent investigations.
本实验室研究旨在探讨可控纳米孔隙率对硅胶粉末增强聚合物复合材料耐磨性的影响,并确定控制这些独特纳米结构材料磨料磨损性能的机制。
通过正硅酸乙酯(TEOS)的水解和缩合反应,使用四种不同的催化剂制备硅胶,以改变所得聚硅酸盐硅烷化的多孔结构,将含有各种引发剂的有机单体(TEGDMA)引入凝胶粉末中形成糊状物。然后将各种糊状物在玻璃模具内聚合。接着使用销盘式磨损试验机记录试样长度和转数。通过回归分析确定磨料磨损率,并通过方差分析和多重比较确定统计差异。使用BET表征填料孔结构,并使用扫描电子显微镜直观检查磨损表面。
注意到实验复合材料的磨损率存在显著差异(p < 0.05)。在所研究的填料孔隙率范围内,发现耐磨性与填料孔体积呈线性相关(R2 = 0.983)。磨损率随填料孔隙率的增加而降低。低孔隙率的HCl催化凝胶制备的复合材料耐磨性相对有限。相比之下,高孔隙率的HF催化凝胶制备的复合材料更耐磨。这些纳米复合材料的磨料磨损抗性不受这些实验中使用的硅烷偶联水平的显著影响。扫描电子显微镜评估表明,更好的耐磨性与磨损表面的精细尺度塑性变形以及填料颗粒未拔出有关。
通过溶胶 - 凝胶法制备多孔颗粒作为填料,在提高光聚合树脂耐磨性方面显示出一定的前景。填料的耐磨性似乎与凝胶颗粒的纳米多孔结构直接相关。与传统牙科复合材料不同,这些材料主要依靠纳米机械耦合来提高耐磨性。这一新原理应有助于后续研究。