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Modification of high-performance polymer composite through high-energy radiation and low-pressure plasma for aerospace and space applications

机译:通过高能辐射和低压等离子体改性高性能聚合物复合材料,用于航空航天

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In this investigation, attempts are made to modify a high-performance polymer such as polybenzimidazole (PBI) (service temperature ranges from -260 degrees C to +400 degrees C) through high-energy radiation and low-pressure plasma to prepare composite with the same polymer. The PBI composites are prepared using an ultrahigh temperature resistant epoxy adhesive to join the two polymer sheets. The service temperature of this adhesive ranges from -260 degrees C to +370 degrees C, and in addition, this adhesive has excellent resistance to most acids, alkalis, solvents, corrosive agents, radiation, and fire, making it extremely useful for aerospace and space applications. Prior to preparing the composite, the surface of the PBI is ultrasonically cleaned by acetone followed by its modification through high-energy radiation for 6 h in the pool of a SLOWPOKE-2 (safe low power critical experiment) nuclear reactor, which produces a mixed field of thermal and epithermal neutrons, energetic electrons, and protons, and gamma-rays, with a dose rate of 37 kGy/h and low-pressure plasma through 13.56 MHz RF glow discharge for 120 s at 100 W of power using nitrogen as process gas, to essentially increase the surface energy of the polymer, leading to substantial improvement of its adhesion characteristics. Prior to joining, the polymer surfaces are characterized by estimating surface energy and electron spectroscopy for chemical analysis (ESCA). To determine the joint strength, tensile lap shear tests are performed according to ASTM D 5868-95 standard. Another set of experiments is carried out by exposing the low-pressure plasma-modified polymer joint under the SLOWPOKE-2 nuclear for 6 h. Considerable increase in the joint strength is observed, when the polymer surface is modified by either high-energy radiation or low-pressure plasma. There is further significant increase in joint strength, when the polymer surface is first modified by low-pressure plasma followed by exposing the joint under high-energy radiation. To simulate with spatial conditions, the joints are exposed to cryogenic (-196 degrees C) and high temperatures (+300 degrees C) for 100 h. Then, tensile lap shear tests are carried out to determine the effects of these environments on the joint strength. It is observed that when these polymeric joints are exposed to these climatic conditions, the joints could retain their strength of about 95% of that of joints tested under ambient conditions. Finally, to understand the behavior of ultrahigh temperature resistant epoxy adhesive bonding of PBI, the fractured surfaces of the joints are examined by scanning electron microscope. It is observed that there is considerable interfacial failure in the case of unmodified polymer-to-polymer joint whereas surface-modified polymer essentially fails cohesively within the adhesive. Therefore, this high-performance polymer composite could be highly useful for structural applications in space and aerospace. (c) 2006 Wiley Periodicals, Inc.
机译:在这项研究中,尝试通过高能辐射和低压等离子体改性高性能聚合物,例如聚苯并咪唑(PBI)(使用温度范围为-260℃至+400℃),以制备具有相同的聚合物。 PBI复合材料是使用耐超高温环氧粘合剂将两个聚合物片材连接在一起而制备的。该胶粘剂的使用温度范围为-260℃至+370℃,此外,该胶粘剂对大多数酸,碱,溶剂,腐蚀剂,辐射和火都具有出色的耐受性,使其非常适用于航空航天和空间应用。在制备复合材料之前,先用丙酮对PBI的表面进行超声波清洗,然后在SLOWPOKE-2(安全的低功率关键实验)核反应堆中通过高能辐射对其进行改性6小时,从而产生混合气体。使用氮作为工艺,以13.kMHz RF辉光放电通过120 s的13.56 MHz RF辉光放电,以37 kGy / h的剂量率,在热和超热中子,高能电子,质子和伽玛射线的范围内以120 k s的剂量率气体,从而实质上增加了聚合物的表面能,从而导致其粘合特性的显着改善。在连接之前,聚合物表面的特征是通过估计表面能和电子光谱进行化学分析(ESCA)。为了确定接头强度,根据ASTM D 5868-95标准进行了拉伸搭接剪切试验。另一组实验是通过将低压等离子改性的聚合物接头在SLOWPOKE-2核下暴露6小时来进行的。当通过高能辐射或低压等离子体对聚合物表面进行改性时,可观察到接头强度的显着提高。当首先通过低压等离子体对聚合物表面进行改性,然后将接头暴露于高能辐射下时,接头强度会进一步显着提高。为了模拟空间条件,将关节暴露于低温(-196摄氏度)和高温(+300摄氏度)下100小时。然后,进行拉伸搭接剪切试验,以确定这些环境对接头强度的影响。观察到,当这些聚合物接头暴露于这些气候条件下时,该接头可以保持其强度为在环境条件下测试的接头强度的约95%。最后,为了了解PBI的超高温环氧胶粘接性能,通过扫描电子显微镜检查了接头的断裂表面。观察到,在未改性的聚合物-聚合物接合的情况下,存在相当大的界面破坏,而表面改性的聚合物在粘合剂内本质上内聚地破坏。因此,这种高性能的聚合物复合材料对于空间和航空航天领域的结构应用可能非常有用。 (c)2006年Wiley Periodicals,Inc.

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