Saeb Mohammad Reza, Bakhshandeh Ehsan, Khonakdar Hossein Ali, Mäder Edith, Scheffler Christina, Heinrich Gert
Department of Resin and Additives, Institute for Color Science and Technology, P.O. Box 16765-654, Tehran, Iran.
Department of Polymer Processing, Iran Polymer and Petrochemical Institute, Tehran 14965-115, Iran ; Leibniz-Institute of Polymer Research Dresden, 01069 Dresden, Germany.
ScientificWorldJournal. 2013 Nov 19;2013:703708. doi: 10.1155/2013/703708.
The current paper provides an overview to emphasize the role of functionalization of multiwalled carbon nanotubes (MWCNTs) in manipulating cure kinetics of epoxy nanocomposites, which itself determines ultimate properties of the resulting compound. In this regard, the most commonly used functionalization schemes, that is, carboxylation and amidation, are thoroughly surveyed to highlight the role of functionalized nanotubes in controlling the rate of autocatalytic and vitrification kinetics. The current literature elucidates that the mechanism of curing in epoxy/MWCNTs nanocomposites remains almost unaffected by the functionalization of carbon nanotubes. On the other hand, early stage facilitation of autocatalytic reactions in the presence of MWCNTs bearing amine groups has been addressed by several researchers. When carboxylated nanotubes were used to modify MWCNTs, the rate of such reactions diminished as a consequence of heterogeneous dispersion within the epoxy matrix. At later stages of curing, however, the prolonged vitrification was seen to be dominant. Thus, the type of functional groups covalently located on the surface of MWCNTs directly affects the degree of polymer-nanotube interaction followed by enhancement of curing reaction. Our survey demonstrated that most widespread efforts ever made to represent multifarious surface-treated MWCNTs have not been directed towards preparation of epoxy nanocomposites, but they could result in property synergism.
本文提供了一个概述,以强调多壁碳纳米管(MWCNTs)功能化在控制环氧纳米复合材料固化动力学方面的作用,而固化动力学本身决定了所得化合物的最终性能。在这方面,对最常用的功能化方案,即羧基化和酰胺化,进行了全面研究,以突出功能化纳米管在控制自催化和玻璃化动力学速率方面的作用。现有文献表明,环氧/MWCNTs纳米复合材料的固化机理几乎不受碳纳米管功能化的影响。另一方面,几位研究人员探讨了在存在含胺基MWCNTs的情况下自催化反应的早期促进作用。当使用羧基化纳米管对MWCNTs进行改性时,由于在环氧基质中的不均匀分散,此类反应的速率降低。然而,在固化后期,延长的玻璃化现象占主导。因此,共价连接在MWCNTs表面的官能团类型直接影响聚合物-纳米管相互作用的程度,进而增强固化反应。我们的研究表明,以往大多数用于表征各种表面处理过的MWCNTs的工作并非针对环氧纳米复合材料的制备,但它们可能会产生性能协同效应。