Krause W R, Park S H, Straup R A
Division of Biomedical Engineering, Virginia Commonwealth University, Richmond 23298.
J Biomed Mater Res. 1989 Oct;23(10):1195-211. doi: 10.1002/jbm.820231008.
The use of short glass fibers as a filler for dental restorations or cement resins have not been examined extensively. The mechanical properties and untreated glass fibers (5 microns dia x 25 microns) in Bis-phenol A glycidyl methacrylate (BIS-GMA) diluted with triethylene-glycol dimethacrylate (TEGDMA) resin were investigated for possible use as a restorative dental composite or bone cement. Compression, uniaxial tension and fracture toughness tests were conducted for each filler composite mixtures of 40, 50, 60 and 70%. Set time and maximum temperature of polymerization were determined. The results show that the elastic modulus, tensile strength and compressive strength are dependent on the percent of filler content. Elastic modulus and compressive yield (0.2%) strength of silane treated glass fibers filled composite increased from 2.26 to 4.59 GPa and 43.3 to 66.6 MPa, respectively, wtih increasing the filler content while the tensile strength decreased from 26.7 to 18.6 MPa. The elastic modulus of the untreated composite was less than that of the silane treated fiber composite. The tensile strength and compressive strengths were 20 to 50% lower than those of silane treated composites. The fracture toughness of the silane treated glass fiber additions were not significantly different from the untreated additions. The highest fracture toughness was obtained at 50% filler content with 1.65 MPa m.5. Set time increased from 3.5 to 7.7 minutes with increased filler content and peak temperature dropped from 68.3 to 34 degrees C. The results of this study indicate that the addition of silane coated glass fiber to BIS-GMA resin increased the elastic modulus, tensile and compressive strengths compared with non-treated fibers. The addition of either treated or non-treated fibers increased the set time of the material and decreased the maximum temperature.
短玻璃纤维作为牙科修复材料或粘结树脂的填充剂尚未得到广泛研究。研究了用二缩三乙二醇二甲基丙烯酸酯(TEGDMA)稀释的双酚A甲基丙烯酸缩水甘油酯(BIS-GMA)树脂中未处理的玻璃纤维(直径5微米×长25微米)作为牙科修复复合材料或骨水泥的潜在用途。对40%、50%、60%和70%的每种填充复合材料混合物进行了压缩、单轴拉伸和断裂韧性测试。测定了固化时间和聚合最高温度。结果表明,弹性模量、拉伸强度和抗压强度取决于填料含量的百分比。随着填料含量的增加,硅烷处理的玻璃纤维填充复合材料的弹性模量和抗压屈服(0.2%)强度分别从2.26 GPa增加到4.59 GPa和从43.3 MPa增加到66.6 MPa,而拉伸强度从26.7 MPa降低到18.6 MPa。未处理复合材料的弹性模量小于硅烷处理纤维复合材料的弹性模量。其拉伸强度和抗压强度比硅烷处理的复合材料低20%至50%。硅烷处理的玻璃纤维添加物的断裂韧性与未处理的添加物没有显著差异。在填料含量为50%时,断裂韧性最高,为1.65 MPa·m0.5。随着填料含量的增加,固化时间从3.5分钟增加到7.7分钟,峰值温度从68.3℃降至34℃。本研究结果表明,与未处理的纤维相比,向BIS-GMA树脂中添加硅烷涂层玻璃纤维可提高弹性模量、拉伸强度和抗压强度。添加处理过的或未处理的纤维都会增加材料的固化时间并降低最高温度。