个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:吉林大学
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理
办公地点:西部校区化工实验楼A207
联系方式:13052731242
电子邮箱:zyb1104@dlut.edu.cn
In situ Formation of Mildly Oxidized Graphene Oxide/Polydicyclopentadiene Composite and Reinforced Mechanical and Thermal Performances
点击次数:
论文类型:期刊论文
发表时间:2014-06-03
发表刊物:JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY
收录刊物:SCIE、EI、Scopus
卷号:51
期号:6
页面范围:514-521
ISSN号:1060-1325
关键字:MOGO; polydicyclopentadiene; ROMP; in situ; crosslinking; mechanical properties; thermal stability
摘要:A series of mildly oxidized graphene oxide (MOGO) reinforced polydicyclopentadiene composites (MOGO/polyDCPD) were prepared via the in situ polymerization of DCPD in the presence of MOGO using ring-opening metathesis polymerization (ROMP). The inter-crosslinking networks between MOGO and polyDCPD backbones formed the reinforced composite structures, examined qualitatively by swelling tests. Bending tests, DMA and TGA measurements were employed to study the optimal loading content of MOGO for achieving the best mechanical and thermal properties of MOGO/polyDCPD composites. The results showed that the maximum mechanical performance was achieved with 0.1wt% of MOGO loading. Excess MOGO led to decreased mechanical properties due to the poor solubility and uneven distribution of MOGO in the polymer matrix, which was confirmed by SEM. Meanwhile, the thermal stability of MOGO/polyDCPD composites showed a similar trend. The decomposition temperature at 10wt% weight loss was significantly increased compared with the unfilled polyDCPD, but decreased with composition of MOGO above 0.1wt%. The addition of MOGO may not only inhibit the back-biting from the catalyst and the formation of low molecular weight oligomers in the polymer, but also covalently immobilize them on its flake.