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In the present study, carbon nanotubes (CNTs) were grown up on nickel‐coated carbon textiles utilizing acetylene gas as a carbon precursor in an isothermal CVD reactor. The effects of CNT coating time (0 to 25 min) in the carbon textile‐phenolic composites (CPCs) prepared via conventional hand‐layup technique followed by compression molding were assessed using microstructures, static and dynamic mechanical thermal analysis, density and electrical properties. Significant improvement was observed in static as well as dynamic mechanical properties and electrical properties for all the CNT coated samples. Though, 15 min coating time gives the optimum results. The results showed ~71, 74, 62, 67, 38, and 45% increment in storage modulus, loss modulus, flexural strength, flexural modulus, tensile strength, Young's modulus, respectively. Furthermore, huge improvement (707%) in electrical conductivity and significant enrichment in thermal stability mark CNTs coated carbon textile as the efficient alternative reinforcement for high‐performance thermo‐structural applications such as aerospace and automotive fields. [ABSTRACT FROM AUTHOR]

Polymer matrix composites reinforced with carbonous fillers are of significant commercial importance thanks to their vast application base. As the performance of such composites largely depends on matrix–filler interaction, the present study is focused on the impact of surface chemical states of polymer matrix and carbonous filler on the viscoelastic performance of the composites. Here we report investigation of the filler–matrix interface through spectroscopic techniques such as X‐ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Viscoelastic properties of various polymer matrix composites prepared by varying the filler volume fraction and/or the matrix/filler type have been studied through dynamic mechanical thermal analysis. Further, to understand the matrix–filler interaction, correlations between viscoelastic parameters and various structural parameters such as the surface area of filler and the surface chemical states of filler/matrix obtained through XPS have been studied. Strong correlations between the viscoelastic parameters and the matrix/filler surface chemical states have been observed, suggesting the XPS as an important tool to study the role of the surface functionalities present on the matrix/filler surface to define the matrix–filler interaction. The filler surface functionalities such as C bound O have been found more compatible with the polymers having aromatic ring in the repeat unit. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 137, 48660. [ABSTRACT FROM AUTHOR]

ABSTRACT This study explores the synergistic effect of aluminium phosphate (ALP) nanoparticles and tungstophosphoric acid (TPA) on the physicochemical properties of sulfonated poly ether ether ketone (SPEEK) nanocomposite membranes. SPEEK/TPA/ALP nanocomposite containing optimum TPA (10 wt %) and varying ALP content (3-10 wt %) are fabricated to investigate the effect of ALP nanoparticles on membrane properties. Experimental results reveal that nanocomposite membrane containing 3 wt % ALP nanoparticles and 10 wt % TPA exhibits 3.3 and 18.8 times higher proton conductivity compared to 10 wt % TPA filled SPEEK composite membrane and reference SPEEK membrane. ALP nanoparticles help in retaining water within the membranes and thus 59.4% reduction in water desorption rate is achieved compared to SPEEK/TPA membrane. The leaching of TPA is reduced by 34.5% which helps in retaining membrane properties. Membranes are thermally stable up to 200°C. Microstructure of the composite films is investigated by scanning electron microscope. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 42952. [ABSTRACT FROM AUTHOR]

Poly(ether ether ketone), PEEK, was functionalized by addition of pendant functional groups, that is, acetyl, carboxylic, acyl chloride, amide, and amine groups in the benzene ring of polymer backbone without substituting the parent (ether or ketonic) functional groups of polymer to improve the mechanical and surface adhesivity with acellular inorganic biomaterials. The functional groups of virgin PEEK and functionalized PEEK were identified by Fourier transform infrared spectroscopy and 13C nuclear magnetic resonance. The crystallinity was studied by X-ray diffraction and further supported by differential scanning calorimetry (DSC) analysis. Similarly, the change in glass transition temperature was confirmed by the DSC and dynamic mechanical analysis (DMA). The improved mechanical property was also evaluated by DMA. The excellent surface adhesivity and bioactivity were revealed by acellular in vitro test using simulated body fluid. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 [ABSTRACT FROM AUTHOR]