Freiburg Materials Research Center and Institute for Macromolecular Chemistry of the University of Freiburg, Stefan-Meier-Strasse 31, D-79117 Freiburg, Germany.
Macromol Rapid Commun. 2013 Aug;34(15):1249-55. doi: 10.1002/marc.201300363. Epub 2013 Jul 9.
Graphene functionalization by hydroxyalkylation and grafting with polyether polyols enables polyurethane (PU) nanocomposites formation by in situ polymerization with isocyanates combined with effective covalent interfacial coupling. Functionalized graphene (FG) hydroxylation is achieved either by alkylation, transesterification, or grafting of thermally reduced graphite oxide. In the presence of K2 CO3 as catalyst the reaction of FG-OH with ethylene carbonate at 180 °C affords hydroxyethylated FG, whereas transesterification with castor oil produces riconoleiate-modified FG polyols. In the "grafting-from" process, FG-alkoholate macro initiators initiate the graft polymerization of propylene oxide to produce hybrid FG polyols containing 38 and 59 wt% oligopropylene oxide. In the "grafting-to" process 3-ethyl-3-hydroxymethyl-oxetane is cationically polymerized onto FG-OH, producing novel hyperbranched FG-based polyether polyols. Whereas hydroxylation and grafting of FG greatly improve FG dispersion in organic solvents, polyols and even PU, as confirmed by transmission electron microscopy, matrix reinforcement of FG/PU is impaired by increasing alkyl chain length and polyol graft copolymer content.
通过羟烷基化和与聚醚多元醇接枝对石墨烯进行功能化,使原位聚合与异氰酸酯结合,并通过有效的共价界面偶联,能够形成聚氨酯(PU)纳米复合材料。功能化石墨烯(FG)的羟化可以通过烷基化、酯交换或热还原氧化石墨的接枝来实现。在 K2CO3 作为催化剂的存在下,FG-OH 与碳酸亚乙酯在 180°C 反应得到羟乙基化的 FG,而与蓖麻油的酯交换则产生 ricinoleate 改性的 FG 多元醇。在“从枝接”过程中,FG-醇盐大分子引发剂引发氧化丙烯的接枝聚合,得到含有 38 和 59wt%低聚氧化丙烯的杂化 FG 多元醇。在“接枝到”过程中,3-乙基-3-羟甲基-氧杂环丁烷阳离子聚合到 FG-OH 上,生成新型超支化 FG 基聚醚多元醇。尽管 FG 的羟化和接枝大大改善了 FG 在有机溶剂、多元醇甚至 PU 中的分散性,但正如透射电子显微镜所证实的那样,FG/PU 的基质增强因烷基链长度和多元醇接枝共聚物含量的增加而受到损害。