首页> 外文期刊>The Journal of Prosthetic Dentistry >Light-polymerized compomers: coefficient of thermal expansion and microhardness.
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Light-polymerized compomers: coefficient of thermal expansion and microhardness.

机译:轻聚体:热膨胀系数和显微硬度。

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STATEMENT OF PROBLEM: The relationship between the filler content, coefficient of thermal expansion, and microhardness of commercial light-polymerized compomers has not been fully investigated. PURPOSE: This study evaluated the effect of filler content on the coefficient of thermal expansion and microhardness of 3 commercially available light-polymerized compomers. MATERIAL AND METHODS: Five specimens each from 3 commercially available compomers (Compoglass F, Elan and F2000) were evaluated. Linear thermal expansion (microm/ degrees C) was measured with a thermomechanical analyzer in the temperature range 20 degrees to 80 degrees C with increments of 10 degrees C. Standardized specimens were prepared in a metal die (1.5 x 2 x 12 mm) and polymerized for 40 seconds at 700 mW/cm(2) light intensity. The microhardness of 5 specimens from each of 3 compomers were measured with a Vickers hardness tester under a 15-second dwell time and 200-g load conditions. The specimens were polymerized at 700 mW/cm(2) intensity for 40 seconds after placing the compomers into a round aluminum mold. Differences in thermal expansion and microhardness among the compomers evaluated were statistically analyzed by use of one-way analysis of variance at P<.01 significance level, with differences assessed by use of Duncan's multiple range post hoc test. RESULTS: The coefficients of thermal expansion of Compoglass F (54.17 +/- 0.54 microm/ degrees C), Elan (40.94 +/- 0.78 microm/ degrees C) and F2000 (24.43 +/- 89 microm/ degrees C) were almost linear in the temperature range 25 degrees to 80 degrees C for all 3 compomers (r >.99). Inverse correlations between the %wt of filler and the coefficient of thermal expansion (r = -0.98, P<.0001), as well as between the microhardness and the coefficient of thermal expansion (r = -0.98, P<.0001) were observed. On the other hand, a linear correlation between the %wt of filler and microhardness of compomers was exhibited (r = -0.96, P<.0001). The microhardness values for Compoglass F, Elan, and F2000 were 43.82 +/- 1.62, 58.16 +/- 1.90, and 72.94 +/- 3.29, respectively. CONCLUSION: Within the limitations of this study, an inverse correlation between percent weight of filler and coefficient of thermal expansion, and a linear correlation between percent weight of filler and microhardness was observed for the evaluated compomers.
机译:问题陈述:尚未完全研究商品轻聚合复合体的填料含量,热膨胀系数和显微硬度之间的关系。目的:本研究评估了填料含量对3种市售轻聚合复合体的热膨胀系数和显微硬度的影响。材料与方法:分别从3种市售复合体(Compoglass F,Elan和F2000)中评估了5个样品。使用热机械分析仪在20到80摄氏度的温度范围内以10摄氏度的增量测量线性热膨胀(微米/摄氏度)。在金属模具(1.5 x 2 x 12毫米)中制备标准化样品并聚合在700 mW / cm(2)的光强度下持续40秒。在15秒的停留时间和200 g的负载条件下,用维氏硬度计测量来自3种复合物的5种样品的显微硬度。将复合材料放入圆形铝模中后,将样品以700 mW / cm(2)的强度聚合40秒。通过单因素方差分析在P <.01显着性水平上对统计评估的复合物之间的热膨胀和显微硬度差异进行统计分析,并使用Duncan多范围事后检验评估差异。结果:Compoglass F(54.17 +/- 0.54 microm /摄氏度),Elan(40.94 +/- 0.78微米/摄氏度)和F2000(24.43 +/- 89微米/摄氏度)的热膨胀系数几乎是线性的所有3种复合物的温度范围为25到80摄氏度(r> .99)。填料的%wt与热膨胀系数(r = -0.98,P <.0001),显微硬度与热膨胀系数(r = -0.98,P <.0001)之间呈负相关。观测到的。另一方面,显示出填料的%wt与复合体的显微硬度之间的线性相关性(r = -0.96,P <.0001)。 Compoglass F,Elan和F2000的显微硬度值分别为43.82 +/- 1.62、58.16 +/- 1.90和72.94 +/- 3.29。结论:在本研究的范围内,观察到的复合物的填充物重量百分数与热膨胀系数成反比,并且填充物重量百分数与显微硬度成线性关系。

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