Effect of MWNTs and SiC-Coated MWNTs on Properties of PEEK/LCP Blend

Multiwall carbon nanotubes (MWNTs) were modified with polycarbosilane-derived silicon carbide (SiC) to improve its dispersion in the polymer matrix. PEEK/LCP/MWNTs nanocomposites were prepared by melt blending. TEM images show the improved dispersion of SiC-coated MWNTs against agglomerated structure of pure MWNTs in the blend. FESEM images shows better fibrillation of LCP in presence of SiC-coated MWNTs. TGA reveals that nanocomposites with SiC-coated MWNTs shows higher thermal stability than MWNTs filled blend system. Based on enhanced dispersion, storage modulus, tensile modulus and tensile strength were increased drastically with the incorporation of SiC-coated MWNTs. Glass transition temperature of the nanocomposites shows significant improvement with the incorporation of MWNTs

Recent Advances in Graphene Based Polymer Composites

This paper reviews recent advances in the modification of graphene and the fabrication of graphene-based polymer nanocomposites. Recently, graphene has attracted both academic and industrial interest because it can produce a dramatic improvement in properties at very low filler content. The modification of graphene/graphene oxide and the utilization of these materials in the fabrication of nanocomposites with different polymer matrixes have been explored. Different organic polymers have been used to fabricate graphene filled polymer nanocomposites by a range of methods. In the case of modified graphene-based polymer nanocomposites, the percolation threshold can be achieved at a very lower filler loading. Herein, the structure, preparation and properties of polymer/graphene nanocomposites are discussed in general along with detailed examples drawn from the scientific literature. (C) 2010 Elsevier Ltd. All rights reserved

In-situ synthesis and characterization of electrically conductive polypyrrole/graphene nanocomposites

Polypyrrole (PPy)/graphene (GR) nanocomposites were successfully prepared via in-situ polymerization of graphite oxide (GO) and pyrrole monomer followed by chemical reduction using hydrazine monohydrate. The large surface area and high aspect ratio of the in-situ generated graphene played an important role in justifying the noticeable improvements in electrical conductivity of the prepared composites via chemical reduction. X-ray photoelectron spectroscopy (XPS) analysis revealed the removal of oxygen functionality from the GO surface after reduction and the bonding structure of the reduced composites were further determined from FTIR and Raman spectroscopic analysis. For PPy/GR composite, intensity ratio between D band and G band was high (w1.17), indicating an increased number of c-sp2 domains that were formed during the reduction process. A reasonable improvement in thermal stability of the reduced composite was also observed. Transmission electron microscopy (TEM) observations indicated the dispersion of the graphene nanosheets within the PPy matrix

Polymer membranes for high temperature proton exchange membrane fuel cell: recent advances and challenge

Proton-exchange membrane fuel cells (PEMFCs) are considered to be a promising technology for efficient power generation in the 21st century. Currently, high temperature proton exchange membrane fuel cells (HT-PEMFC) offer several advantages, such as high proton conductivity, low permeability to fuel, low electro-osmotic drag coefficient, good chemical/thermal stability, good mechanical properties and low cost. Owing to the aforementioned features, high temperature proton exchange membrane fuel cells have been utilized more widely compared to low temperature proton exchange membrane fuel cells, which contain certain limitations, such as carbon monoxide poisoning, heat management, water leaching, etc. This review examines the inspiration for HT-PEMFC development, the technological constraints, and recent advances. Various classes of polymers, such as sulfonated hydrocarbon polymers, acid–base polymers and blend polymers, have been analyzed to fulfill the key requirements of high temperature operation of proton exchange membrane fuel cells (PEMFC). The effect of inorganic additives on the performance of HT-PEMFC has been scrutinized. A detailed discussion of the synthesis of polymer, membrane fabrication and physicochemical characterizations is provided. The proton conductivity and cell performance of the polymeric membranes can be improved by high temperature treatment. The mechanical and water retention properties have shown significant improvement., However, there is scope for further research from the perspective of achieving improvements in certain areas, such as optimizing the thermal and chemical stability of the polymer, acid management, and the integral interface between the electrode and membrane