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Mechanical, thermal, and viscoelastic response of novel in situ CTBN/POSS/epoxy hybrid composite system

机译:新型原位CTBN / POSS /环氧树脂混合复合体系的机械,热和粘弹性响应

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The present study focuses on the preparation of a novel hybrid epoxy nanocomposite with glycidyl polyhedral oligomeric silsesquioxane (POSS) as nanofiller, carboxyl terminated poly(acrylonitrile-co-butadiene) (CTBN) as modifying agent and diglycidyl ether of bisphenol A (DGEBA) as matrix polymer. The reaction between DGEBA, CTBN, and glycidyl POSS was carefully monitored and interpreted by using Fourier transform infrared (FTIR) and differential scanning calorimetry (DSC). An exclusive mechanism of the reaction between the modifier, nanofiller, and the matrix is proposed herein, which attempts to explains the chemistry behind the formation of an intricate network between POSS, CTBN, and DGEBA. The mechanical properties, such as tensile strength, and fracture toughness, were also carefully examined. The fracture toughness increases for epoxy/CTBN, epoxy/POSS, and epoxy/CTBN/POSS hybrid systems with respect to neat epoxy, but for hybrid composites toughening capability of soft rubber particles is lost by the presence of POSS. Field emission scanning electron micrographs (FESEM) of fractured surfaces were examined to understand the toughening mechanism. The viscoelastic properties of epoxy/CTBN, epoxy/POSS, and epoxy/CTBN/POSS hybrid systems were analyzed using dynamic mechanical thermal analysis (DMTA). The storage modulus shows a complex behavior for the epoxy/POSS composites due to the existence of lower and higher crosslink density sites. However, the storage modulus of the epoxy phase decreases with the addition of soft CTBN phase. The T-g corresponding to epoxy-rich phase was evident from the dynamic mechanical spectrum. For hybrid systems, the T-g is intermediate between the epoxy/rubber and epoxy/POSS systems. Finally, TGA (thermo gravimetric analysis) studies were employed to evaluate the thermal stability of prepared blends and composites. POLYM. COMPOS., 37:2109-2120, 2016. (c) 2015 Society of Plastics Engineers
机译:本研究致力于制备一种新型的混合环氧纳米复合材料,以缩水甘油基多面体低聚倍半硅氧烷(POSS)为纳米填料,以羧基封端的聚(丙烯腈-共-丁二烯)(CTBN)为改性剂,以双酚A(DGEBA)为二缩水甘油醚基质聚合物。使用傅里叶变换红外(FTIR)和差示扫描量热法(DSC)仔细监控和解释DGEBA,CTBN和缩水甘油基POSS之间的反应。本文提出了改性剂,纳米填料和基质之间反应的排他性机理,试图解释在POSS,CTBN和DGEBA之间形成复杂网络的背后的化学反应。还仔细检查了机械性能,例如拉伸强度和断裂韧性。相对于纯环氧树脂,环氧/ CTBN,环氧/ POSS和环氧/ CTBN / POSS混合体系的断裂韧性增加,但对于混合复合材料,由于存在POSS而使软橡胶颗粒的增韧能力丧失。检查断裂表面的场发射扫描电子显微照片(FESEM)以了解增韧机理。使用动态机械热分析(DMTA)分析了环氧/ CTBN,环氧/ POSS和环氧/ CTBN / POSS混合体系的粘弹性。由于存在较低和较高的交联密度位点,因此储能模量对于环氧/ POSS复合材料表现出复杂的行为。然而,随着软CTBN相的加入,环氧相的储能模量降低。从动态机械光谱可以明显看出对应于富环氧相的T-g。对于混合系统,T-g在环氧/橡胶和环氧/ POSS系统之间。最后,采用TGA(热重分析)研究来评估所制备的共混物和复合材料的热稳定性。 POLYM。 COMPOS。,37:2109-2120,2016.(c)2015年塑料工程师学会

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