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Grafting poly (methyl methacrylate) from azo-functionalized graphene nanolayers via reverse atom transfer radical polymerization

机译:通过反向原子转移自由基聚合从偶氮官能化的石墨烯纳米层接枝聚甲基丙烯酸甲酯

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摘要

Graphene oxide (GO) was functionalized with (3-aminopropyl)triethoxysilane (APTES) from hydroxyl groups. Subsequently, 4,4'-azobis(4-cyanopentanoic acid) (ACPA) was attached to the APTES-functionalized GO to yield azo-anchored graphene (GOAzo). Then, grafting from reverse atom transfer radical polymerization of methyl methacrylate in the presence of GOAzo in different weight percents was carried out. The grafting ratio of APTES and ACPA was calculated to be 41 and 26 % via the data of N content from elemental analysis. Successful functionalization of GO with APTES, ACPA, and poly(methyl methacrylate) (PMMA) was also proved by XPS and FTIR. SEC results show that molecular weight and PDI values of the attached chains are higher. Expansion of graphene interlayer spacing and crystal structure of carbon in different graphenes were evaluated by XRD and Raman spectroscopy, respectively. Graft density of modifier and PMMA in various graphenes was evaluated by TGA. Finally, morphology of graphene nanolayers was studied by scanning and transmission electron microscopies.
机译:用(3-氨基丙基)三乙氧基硅烷(APTES)从羟基官能化氧化石墨烯(GO)。随后,将4,4'-偶氮双(4-氰基戊酸)(ACPA)连接到APTES官能化的GO上,生成偶氮固定的石墨烯(GOAzo)。然后,在不同重量百分比的GOAzo存在下,进行甲基丙烯酸甲酯的反向原子转移自由基聚合的接枝。根据元素分析的N含量数据,APTES和ACPA的接枝率分别为41%和26%。 XPS和FTIR也证明了可以用APTES,ACPA和聚甲基丙烯酸甲酯(PMMA)成功完成GO功能化。 SEC结果表明,连接链的分子量和PDI值较高。分别通过XRD和拉曼光谱法评估了不同石墨烯中石墨烯层间距的扩展和碳的晶体结构。通过TGA评估改性剂和PMMA在各种石墨烯中的接枝密度。最后,通过扫描和透射电子显微镜研究了石墨烯纳米层的形态。

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