Longun Jimmy, Iroh Jude O
Department of Mechanical and Materials Engineering, University of Cincinnati, Cincinnati, OH 45221, USA.
Polymers (Basel). 2023 Nov 16;15(22):4427. doi: 10.3390/polym15224427.
Neat polyimide films are known to be dense and rigid. They are therefore not suitable for use in membranes, sensors and sustainable energy storage applications. In this study, a novel technique has been used to simultaneously improve the porosity, rigidity, damping ability and impact resistance of polyimide membranes. It is demonstrated that dispersion of a small amount of polyaniline copolymer-modified clay of about 0.25-0.5 wt.% into the polyimide matrix resulted in an enhanced storage modulus while maintaining high damping ability and glass transition temperature, T. Novel polyimide/substituted polyaniline-copolymer-clay nanocomposite membranes containing poly(-ethyl-aniline-co-aniline-2-sulfonic-acid)-modified-clay (SPNEAC) was successfully prepared and incorporated into the polyimide matrix to form modified clay/polyimide nanocomposites. UV-Vis analysis of the nanocomposite films shows that the optical transparency of the SPNEAC-PI nanocomposite membranes decreased with increasing SPNEAC concentration due to the high UV-Vis absorption of SPNEAC. Transmittance of about 3% was observed in the nanocomposite membrane containing 5 wt.% modified clay at 500 nm wavelength, which is significantly lower than that for the neat PI membrane of about 36%. The dispersion of SPNEAC containing a high concentration of clay (≥40 wt.% clay), in polyimide matrix, resulted in the attainment of a higher degree of imidization than was possible for the organoclay/polyimide nanocomposite. This behavior is believed to be due to the synergistic interaction between PI and SPNEAC. A correlation of the morphology and elastic modulus of the SPNEAC2/PI nanocomposites shows that at low loading of SPNEAC 2 ≤ 0.5 wt.%, the cross-sectional morphology of the composite is an open, spiky, weblike structure with a storage modulus of about 1 GPa, but it progressively evolves into densely packed microspheroids with storage moduli of ≥2 GPa at 10 wt.% SPNEAC2. The impact energy of SPNEAC/PI composites, calculated from the α-transition peak area, increased with increasing SPNEAC loading and were about 4 times that of neat PI at 10 wt.% SPNEAC.
纯聚酰亚胺薄膜质地致密且坚硬。因此,它们不适用于膜、传感器和可持续储能应用。在本研究中,一种新技术被用于同时提高聚酰亚胺膜的孔隙率、硬度、阻尼能力和抗冲击性。结果表明,将少量约0.25 - 0.5 wt.%的聚苯胺共聚物改性粘土分散到聚酰亚胺基体中,可提高储能模量,同时保持高阻尼能力和玻璃化转变温度T。成功制备了含有聚(-乙基苯胺-共-苯胺-2-磺酸)改性粘土(SPNEAC)的新型聚酰亚胺/取代聚苯胺-共聚物-粘土纳米复合膜,并将其掺入聚酰亚胺基体中形成改性粘土/聚酰亚胺纳米复合材料。纳米复合膜的紫外-可见分析表明,由于SPNEAC的高紫外-可见吸收,SPNEAC-PI纳米复合膜的光学透明度随SPNEAC浓度的增加而降低。在500 nm波长下,含5 wt.%改性粘土的纳米复合膜的透光率约为3%,显著低于纯聚酰亚胺膜的约36%。在聚酰亚胺基体中分散高浓度粘土(≥40 wt.%粘土)的SPNEAC,导致比有机粘土/聚酰亚胺纳米复合材料更高程度的亚胺化。这种行为被认为是由于PI和SPNEAC之间的协同相互作用。SPNEAC2/PI纳米复合材料的形态与弹性模量的相关性表明,在低负载量SPNEAC 2≤0.5 wt.%时,复合材料的横截面形态为开放、尖刺状、网状结构,储能模量约为1 GPa,但在10 wt.% SPNEAC2时逐渐演变为紧密堆积的微球体,储能模量≥2 GPa。由α-转变峰面积计算得出的SPNEAC/PI复合材料的冲击能量随SPNEAC负载量的增加而增加,在10 wt.% SPNEAC时约为纯PI的4倍。