A facile thermodecomposition process to synthesize magnetic graphene nanocomposites (MGNCs) is reported. High-resolution transmission electron microscopy and energy filtered elemental mapping revealed a core@double-shell structure of the nanoparticles with crystalline iron as the core, iron oxide as the inner shell and amorphous Si-S-O compound as the outer shell. The MGNCs demonstrate an extremely fast Cr(VI) removal from the wastewater with a high removal efficiency and with an almost complete removal of Cr(VI) within 5 min. The adsorption kinetics follows the pseudo-second-order model and the novel MGNC adsorbent exhibits better Cr(VI) removal efficiency in solutions with low pH. The large saturation magnetization (96.3 emu/g) of the synthesized nanoparticles allows fast separation of the MGNCs from liquid suspension. By using a permanent magnet, the recycling process of both the MGNC adsorbents and the adsorbed Cr(VI) is more energetically and economically sustainable. The significantly reduced treatment time required to remove the Cr(VI) and the applicability in treating the solutions with low pH make MGNCs promising for the efficient removal of heavy metals from the wastewater.

Carbon nanofibers (CNFs) suspended epoxy resin nanocomposites and the corresponding polymer nanocomposites are fabricated. The surface of CNFs is introduced a functional amine terminated groups via silanization, which in situ react with epoxy monomers. This in situ reaction favors the CNFs dispersion and improves the interfacial interaction between CNFs and monomers. Effects of particle loading, surface treatment and operating temperatures of rheological tests on the complex viscosity, storage modulus and loss modulus are systematically studied. Unique rheological phenomena ''a decreased viscosity with a better dispersion'' are observed and explained in terms of the improved filler dispersion quality. Meanwhile, significant increase in the tensile property and storage modulus is observed and related to the better dispersion and the introduced strong interfacial interaction as revealed by SEM imaging. Finally, electrical conductivity is investigated and an unusual deficiency of surface treatment to improve the electrical conductivity is explained by an insulating coating layer.

In this review paper, the state-of-the-art knowledge of the core-shell multifunctional nanoparticles (MNPs), especially with unique physiochemical properties, is presented. The synthesis methods were summarized from the aspects of both the advantages and the demerits. The core includes the inexpensive and easily oxidized metals and the noble shells include the relatively noble metals, carbon, silica, other oxides, and polymers. The properties including magnetic, optical, anti-corrosion and the surface chemistry of the NPs are thoroughly reviewed. The current status of the applications is reviewed with the detailed examples including the catalysis, giant magnetoresistance (GMR) sensing, electromagnetic interface shielding or microwave absorption, biomedical drug delivery, and the environmental remediation.

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Polyaniline (PANI)/tungsten oxide (WO 3 ) nanocomposite films were fabricated by electropolymerization of aniline monomers onto WO 3 coated indium tin oxide (ITO) glass slides, which were prepared by spin coating technique and followed by annealing at 500 °C for 2 h. The morphology and crystalline structure of the composite films were studied using Fourier transform infrared (FT-IR) spectroscopy, atomic force microscopy (AFM), X-ray diffraction (XRD), and transmission electron microscopy (TEM). The results confirm chemical interactions between the polymer matrix and the WO 3 particles and reveal a well crystallized PANI/WO 3 nanocomposite structure. The optical properties and electrochemical capacitive behaviors of the composite films for electrochromic (EC) and energy storage devices applications were investigated using spectroelectrochemistry (SEC), cyclic voltammetry (CV) and galvanostatic charge−discharge measurements. The composite films show dual electrochromism at both positive and negative potentials arising from PANI and WO 3 , respectively. A coloration efficiency of 98.4 cm 2 C −1 was obtained for the composite film, which was much higher than that of WO 3 (36.3 cm 2 C −1 ) and PANI (50.0 cm 2 C −1 ) thin film. An areal capacitance of 0.025 F cm −2 that is comparable to that of pure PANI (0.075 F cm −2 ) is derived from CV at a scan rate of 5 mV/s with a broader working potential window of 1.3 V. The cyclic stability studies reveal that the composite films exhibit much more enhanced durability and retain significant charge storage or discharge capacity after 1000 charge−discharge cycles. However, pure PANI loses most of the charge storage or discharge capacity after 350 cycles. The chemical bonding between PANI matrix and WO 3 particles is believed to play an important role in enhancing the stability of the nanocomposite film.

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The high performance multi-walled carbon nanotubes (MWNTs) reinforced epoxy polymer nanocomposites (PNCs) have been synthesized at different MWNT loading levels. The surface functionalization of MWNTs with conductive PANI was achieved by using a facile surface initiated polymerization method with the aid of the oxidations of CNTs and subsequent anilines by hexavalent chromium (Cr(VI)) oxidant. The effects of MWNT loading, surface functionalization and temperature on the rheological behaviors of liquid epoxy resin nanosuspensions and on the physicochemical properties of cured solid PNCs were systematically investigated. The glass transition temperature (T g ) of the cured epoxy PNCs filled with functionalized MWNTs obtained from the dynamic mechanical analysis (DMA)test was increased about 6-25 C than that of cured pure epoxy. The PNCs reinforced with functionalized MWNTs demonstrated an enhanced tensile strength than either cured pure epoxy or its PNCs filled with the as-received MWNTs. The electrical conductivity of cured epoxy PNCs with functionalized MWNTs was improved by 5.5 orders of magnitude compared with cured pure epoxy.Thermogravimetric analysis (TGA) revealed an enhanced thermo-stability in the cured epoxy PNCs filled with functionalized MWNTs than that of cured pure epoxy and its PNCs filled with the as-received MWNTs. The observed strong interfacial interaction between MWNTs and the epoxy resin matrix was responsible for the enhanced mechanical tensile strength. The nanocomposite formation mechanism is proposed based on the analysis from Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman and differential scanning calorimetry (DSC) tests.