Electromagnetic interference (EMI) performance materials are urgently needed to relieve the increasing stress over electromagnetic pollution problems arising from the growing demand for electronic and electrical devices. In this work, a novel ultralight (0.15 g/cm(3)) carbon foam was prepared by direct carbonization of phthalonitrile (PN)-based polymer foam aiming to simultaneously achieve high EMI shielding effectiveness (SE) and deliver effective weight reduction without detrimental reduction of the mechanical properties. The carbon foam prepared by this method had specific compressive strength of ∼6.0 MPa·cm(3)/g. High EMI SE of ∼51.2 dB was achieved, contributed by its intrinsic nitrogen-containing structure (3.3 wt% of nitrogen atoms). The primary EMI shielding mechanism of such carbon foam was determined to be absorption. Moreover, the carbon foams showed excellent specific EMI SE of 341.1 dB·cm(3)/g, which was at least 2 times higher than most of the reported material. The remarkable EMI shielding performance combined with high specific compressive strength indicated that the carbon foam could be considered as a low-density and high-performance EMI shielding material for use in areas where mechanical integrity is desired.

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Development of advanced graphene based polymer composites is still confronted with severe challenges due to its poor dispersion caused by restacking, weak interface bonding, and incompatibility with polymer matrices which suppress exertion of the actual potential of graphene sheets in composites. Here, we have demonstrated an efficient chemical modification process with polyethylenimine (PEI) to functionalize graphene oxide which can overcome the above-mentioned drawbacks and also can remarkably increase the overall strength of the nylon 12 composites even at very low graphene loading. Chemical modification was analyzed by various surface characterizations including X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction. Addition of only 0.25 and 0.35 wt % modified GO showed 37% and 54% improvement in tensile strength and 65% and 74% in Young's modulus, respectively, compared with that of the neat polymer. The dynamic mechanical analysis showed ∼39% and 63% increment in storage modulus of the nanocomposites. Moreover, the nanocomposites exhibited significantly high thermal stability (∼15 °C increment by only 0.35 wt %) as compared to neat polymer. Furthermore, the composites rendered outstanding resistance against various chemicals.

Control of surface properties is very important in high performance microfluidic devices because appropriate functionalization of the surface of the microchannel helps to minimize adsorption of certain analytes thus improving its performance. In this regard, both the argon and oxygen plasma techniques have been used to improve the adaption of polymer surfaces to biological environments. However, the less common nitrogen plasma technique has not been used for surface modification of cyclic olefin copolymer (COC) in microfluidic applications. This paper presents a comparative study between the argon, oxygen, and nitrogen plasma treatments with the aim to identify the most suitable process for the development of a smart, disposable chip for the Bio‐MEMS application. The chemical and morphological changes of the plasma modified COC surfaces were characterized using X‐ray photoelectron spectroscopy, atomic force microscopy, and water contact angle measurements. The effect of plasma treatment on the strength of thermally bonded lap‐shear specimens was studied. The influence of plasma treatment on the integrity of thermally sealed microdevices was assessed using burst pressure tests. The plasma treatments had a significant impact on the electroosmosis flow mobility in the microchannels. The hemocompatibility of the various plasma‐modified COC surfaces was determined using the static platelets adhesion experiment. It was shown that the nitrogen plasma treatment was more effective than the argon and oxygen treatments for the modification of COC based microfluidic devices.

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