Xu Shiai, Song Xiaoxue, Cai Yangben
School of Chemical Engineering, Qinghai University, Xining 810016, China.
School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Materials (Basel). 2016 Jul 29;9(8):640. doi: 10.3390/ma9080640.
In order to enhance the compatibilization and interfacial adhesion between epoxy and liquid carboxyl-terminated butadiene acrylonitrile (CTBN) rubber, an initiator was introduced into the mixture and heated to initiate the cross-linking reaction of CTBN. After the addition of curing agents, the CTBN/epoxy blends with a localized interpenetrating network structure were prepared. The mechanical properties and morphologies of pre-crosslinked and non-crosslinked CTBN/epoxy blends were investigated. The results show that the tensile strength, elongation at break and impact strength of pre-crosslinked CTBN/epoxy blends are significantly higher than those of non-crosslinked CTBN/epoxy blends, which is primarily due to the enhanced interfacial strength caused by the chemical bond between the two phases and the localized interpenetrating network structure. Both pre-crosslinked and non-crosslinked CTBN/epoxy blends show a bimodal distribution of micron- and nano-sized rubber particles. However, pre-crosslinked CTBN/epoxy blends have smaller micron-sized rubber particles and larger nano-sized rubber particles than non-crosslinked CTBN/epoxy blends. The dynamic mechanical analysis shows that the storage modulus of pre-crosslinked CTBN/epoxy blends is higher than that of non-crosslinked CTBN/epoxy blends. The glass transition temperature of the CTBN phase in pre-crosslinked CTBN/epoxy blends increases slightly compared with the CTBN/epoxy system. The pre-crosslinking of rubber is a promising method for compatibilization and controlling the morphology of rubber-modified epoxy materials.
为了增强环氧树脂与端羧基丁腈橡胶(CTBN)之间的相容性和界面黏附力,将一种引发剂引入混合物中并加热以引发CTBN的交联反应。加入固化剂后,制备出具有局部互穿网络结构的CTBN/环氧树脂共混物。研究了预交联和未交联的CTBN/环氧树脂共混物的力学性能和形态。结果表明,预交联的CTBN/环氧树脂共混物的拉伸强度、断裂伸长率和冲击强度显著高于未交联的CTBN/环氧树脂共混物,这主要归因于两相之间的化学键和局部互穿网络结构导致的界面强度增强。预交联和未交联的CTBN/环氧树脂共混物均呈现微米级和纳米级橡胶颗粒的双峰分布。然而,预交联的CTBN/环氧树脂共混物比未交联的CTBN/环氧树脂共混物具有更小的微米级橡胶颗粒和更大的纳米级橡胶颗粒。动态力学分析表明,预交联的CTBN/环氧树脂共混物的储能模量高于未交联的CTBN/环氧树脂共混物。与CTBN/环氧树脂体系相比,预交联的CTBN/环氧树脂共混物中CTBN相的玻璃化转变温度略有升高。橡胶的预交联是一种很有前景的使橡胶增韧环氧树脂材料相容并控制其形态的方法。