采用元素分析、红外光谱(FTIR)、X射线光电子能谱(XPS)、拉曼光谱、X射线衍射(XRD)、固体13C核磁共振波谱(13C MAS NMR)、热失重分析(TGA)、导电率测试以及原子力显微镜(AFM)等手段对正丁基氯化镁还原的氧化石墨烯进行了系统的表征.结果表明,正丁基氯化镁可以有效还原氧化石墨烯,随着其用量的增加,氧化石墨烯还原程度增加,碳/氧摩尔比升高,片层间距减小,热稳定性增强,导电率增大(可达3.6!102S/m).还原后部分氧化石墨烯片层发生聚集.
In this paper, we review our recent progress in the synthesis and application of styryl-capped polypropylene （PP-t- St）, an excellent reactive polyolefin that is both convenient and efficient in synthesis and facile and versatile in application for preparing advanced polypropylene materials via macromolecular engineering. The synthesis of PP-t-St is made possible by a unique chain transfer reaction coordinated by a bis-styrenic molecule, such as 1,4-divinylbenzene （DVB） and 1,2-bis（4- vinylphenyl）ethane （BVPE）, and hydrogen in typical C2-symmetric metallocene （e.g. rac-Me2Si（2-Me-4-Ph-Ind）2ZrC12, in association with methylaluminocene, MAO） catalyzed propylene polymerization. The regio-selective 2,1- insertion of the styrenic double bond in DVB or BVPE into the overwhelmingly 1,2-fashioned Zr-PP propagating chain enables substantial dormancy of the catalyst active site, which triggers selective hydrogen chain transfer that, with the formed Zr-H species ultimately saturated by the insertion of propylene monomer, results in an exclusive capping of the afforded PP chains by styryl group at the termination end. With a highly reactive styryl group at chain end, PP-t-St has been used as a facile building block in PP macromolecular engineering together with the employment of state-of-the-art synthetic polymer chemistry to fabricate broad types of new polypropylene architectures.
