吉林大学学报(医学版) ›› 2018, Vol. 44 ›› Issue (05): 968-973.doi: 10.13481/j.1671-587x.20180514

• 基础研究 • 上一篇    下一篇

α-Si3N4与SP1SiO2熔附条件和填料比例对复合树脂性能的影响

李保泉, 刘璐瑶, 张雯雯, 刘可可, 姜婷, 布文奂, 李波, 孙宏晨   

  1. 吉林大学口腔医院实验教学中心, 吉林 长春 130021
  • 收稿日期:2017-10-31 出版日期:2018-09-28 发布日期:2018-11-20
  • 通讯作者: 孙宏晨,教授,博士研究生导师(Tel:0431-88796012,E-mail:hcsun@jlu.edu.cn);李波,副教授,硕士研究生导师(Tel:0431-85579563,E-mail:lbo@jlu.edu.cn) E-mail:hcsun@jlu.edu.cn;lbo@jlu.edu.cn
  • 作者简介:李保泉(1965-),男,吉林省长春市人,教授,医学博士,主要从事口腔材料学方面的研究。
  • 基金资助:
    吉林省科技厅自然科学基金项目资助课题(20170101093JC);吉林省科技厅国际科技合作项目资助课题(20170414053GH);吉林省教育厅"十三五"科学技术研究规划项目资助课题(JJKH20170839KJ);吉林省卫计委青年科技骨干培养计划项目资助课题(2016Q020)

Influence of α-Si3N4 and SP1SiO2 fusing conditions and filler ratios in properities of dental resin composites

LI Baoquan, LIU Luyao, ZHANG Wenwen, LIU Keke, JIANG Ting, BU Wenhuan, LI Bo, SUN Hongchen   

  1. Experimental Teaching Center, Stomatology Hospital, Jilin University, Changchun 130021, China
  • Received:2017-10-31 Online:2018-09-28 Published:2018-11-20

摘要: 目的:检测α-氮化硅(α-Si3N4)与多微孔纳米二氧化硅(SP1SiO2)的最佳熔附温度、熔附时间和最佳填料比例,阐明其对复合树脂性能的影响。方法:将α-Si3N4晶须和SP1SiO2颗粒按质量比5:1混合,以250℃·h-1的升温速度分别升至500℃、650℃、800℃、950℃和1 100℃,并分别保持10 min、30 min和3 h,即为α-Si3N4-SP1SiO2熔附体复合树脂组,同时设立SP1SiO2颗粒组、α-Si3N4晶须组和α-Si3N4与SP1SiO2混合未熔附组(混合组),选择2种市售复合树脂作为对照组。环己烷溶液处理后与树脂基质按质量分数60%充分混合、聚合制作试样,测试挠曲强度并分析其断面扫描电子显微镜(SEM)形貌。再将配比为2:1的α-Si3N4与SP1SiO2混合,最佳熔附条件熔附,环己烷溶液处理后与树脂基质按20%、40%、60%、70%和75%质量分数充分混合、聚合,选择2种市售复合树脂作为对照组,测试挠曲强度并分析其断面SEM形貌。结果:α-Si3N4-SP1SiO2熔附体复合树脂组800℃、30 min时挠曲强度值最大,挠曲强度值均明显高于SP1SiO2颗粒组、α-Si3N4晶须组、混合组和2个对照组(P<0.05),断面SEM形貌与力学性能相符。α-Si3N4-SP1SiO2熔附体复合树脂挠曲强度随着α-Si3N4与SP1SiO2熔附体填料比例从20%增加至60%逐渐增大(P<0.05),填料比例为60%~70%时挠曲强度值增加不明显,填料比例为70%~75%时挠曲强度值减小,填料比例为60%和70%时复合树脂的挠曲强度值均明显高于填料比例为20%、40%和75%时复合树脂及对照组,断面SEM形貌与力学性能相符。结论:α-Si3N4与SP1SiO2最佳熔附条件是800℃处理30 min;α-Si3N4与SP1SiO2熔附体填料最佳比例为70%。

关键词: α-氮化硅, 多微孔纳米二氧化硅, 熔附温度, 熔附时间, 填料比例, 复合树脂

Abstract: Objective:To detect the optimal fusing temperature, the fusing time and the best filler ratio of α-Si3N4 and SP1SiO2, and to clarify their influence in the properities of dental resin composites. Methods:The α-Si3N4 crystalline were mixed with SP1SiO2 particle at the ratio of 5:1(Wt%), and then were sintered under 500℃, 650℃, 800℃, 950℃ and 1 100℃ at a rise rate of 250·h-1 and maintained for 10 min, 30 min and 3 h, respectively(used as α-Si3N4-SP1SiO2 groups).SP1SiO2 particle, α-Si3N4 crystalline, mixed and non-fused α-Si3N4 and SP1SiO2(mixed) groups were set up, and two commercially available resin composites were selected and used as control groups. And they were fully mixed with the resin matrix in 60%(Wt%) after the treatment of cyclohexane solution to make the samples. The flexural strength of specimen was tested and the morphology of section under SEM was analyzed. Then α-Si3N4 was mixed with SP1SiO2 in a ratio of 2:1. It was fused under the optimal fusing conditions. After the treatment of cyclohexane solution, it was mixed and polymerized with the resin matrix in the proportions of 20%, 40%, 60%, 70% and 75%(Wt%), and two kinds of commercially available resin composites were selected and used as control groups. The flexural strength of specimens was tested and the morphology of section under SEM was analyzed. Results:The maximum flexural strength value in α-Si3N4-SP1SiO2 groups was at 800℃ and 30 min(P>0.05);the flexural strength value was significantly higher than those in SP1SiO2 group, α-Si3N4 crystalline group, mixed group and two control groups(P<0.05), and the morphology of section SEM was consistent with the mechanical properties. The flexural strengths of resin composites were increased gradually with the increasing of filler ratios of α-Si3N4 and SP1SiO2 fusion from 20% to 60%(P<0.05); the flexural strength values of resin composites with the proportion of 60%-70% were not increased significantly, the flexural strength values of resin composites with the proportion of 70%-75% were decreased, and the flexural strength values of the resin composites with the proportion of 60% and 70% were significantly higher than those of resin composites with the proportions of 20%, 40%, 75% and control groups; the morphology of section under SEM was consistent with the mechanical properties. Conclusion:The optimum fusing condition for α-Si3N4 and SP1SiO2 is 800℃ for 30 min,and the best filler ratio of α-Si3N4 and SP1SiO2 is 70%.

Key words: α-silicon nitride, more micropore nanometer SiO2, fusing temperature, fusing time, filler ratio, resin composites

中图分类号: 

  • R783.1