Suying Wei

One-Pot Synthesis of Magnetic Graphene Nanocomposites Decorated with Core@Double-shell Nanoparticles for Fast Chromium Removal

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.

Advanced titania nanostructures and composites for lithium ion battery

Owing to the increasing demand of energy and shifting to the renewable energy resources, lithium ion batteries (LIBs) have been considered as the most promising alternative and green technology for energy storage applied in hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and other electric utilities. Owing to its environmental benignity, availability, and stable structure, titanium dioxide (TiO2) is one of the most attractive anode materials of LIBs with high capability, long cycling life, high safety, and low cost. However, the poor electrical conductivity and low diffusion coefficient of Li-ions in TiO2 hamper the advancement of TiO2 as anode materials of LIBs. Therefore, intensive research study has been focused on designing the nanostructures of TiO2 and its composites to reduce the diffusion length of Li-ion insertion/extraction and improve the electrical conductivity of the electrode materials. In this article, the development of TiO2 and its composites in nano-scales including fabrication, characterization of TiO2 nanomaterials, TiO2/carbon composite, and TiO2/metal oxide composites to improve their properties (capacity, cycling performance, and energy density) for LIBs are reviewed. Meanwhile, the mechanisms for influences of the structure, surface morphology, and additives to TiO2 composites on the related properties of TiO2 and TiO2 composites to LIBs are discussed. The new directions of research on this field are proposed.

In situ stabilized carbon nanofiber (CNF) reinforced epoxy nanocomposites

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.

An overview of the engineered graphene nanostructures and nanocomposites

This critical review focuses on the property analysis of graphene and graphene nanocomposites (GNCs) and their demonstrated superior performances in energy storage and conversion, electrochemical- and bio-sensing, environmental remediation and flame retardant application and atomic thickness membrane separation. The performances of graphene and GNCs are strongly dependent on their chemical component, synthetic method, nanoscale morphology, and assembling structure of the hybrids. The current progress in supercapacitor energy storage density, solar cell power conversion efficiency, thermoelectric energy conversion efficiency, electrochemical sensing capability, biosensor sensitivity, heavy metal adsorption capacity and efficiency, photocatalytic degradation rate of organic dye, flame retardant polymer nanocomposites, graphene and porous graphene membranes is discussed with detailed examples through extensive analysis of the literature.

Magnetic polyaniline nanocomposites toward toxic hexavalent chromium removal

The removal of toxic hexavalent chromium (Cr(VI)) from polluted water by magnetic polyaniline (PANI) polymer nanocomposites (PNCs) was investigated. The PNCs were synthesized using a facile surface initiated polymerization (SIP) method and demonstrated unique capability to remove Cr(VI) from polluted solutions with a wide pH range. Complete Cr(VI) removal from a 20.0 mL neutral solution with an initial Cr(VI) concentration of 1.0–3.0 mg L−1 was observed after a 5 min treatment period with a PNC load of 10 mg. The PNC dose of 0.6 g L−1 was found to be sufficient for complete Cr(VI) removal from 20.0 mL of 9.0 mg L−1 Cr(VI) solution. The saturation magnetization was observed to have no obvious decrease after treatment with Cr(VI) solution, and these PNCs could be easily recovered using a permanent magnet and recycled. The Cr(VI) removal kinetics were determined to follow pseudo-first-order behavior with calculated room temperature pseudo-first-order rate constants of 0.185, 0.095 and 0.156 min−1 for the solutions with pH values of 1.0, 7.0 and 11.0, respectively. The Cr(VI) removal mechanism was investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and energy-filter transmission electron microscopy (EFTEM). The results showed that PANI was partially oxidized after treatment with Cr(VI) solution, with Cr(VI) being reduced to Cr(III). The EFTEM observation indicated that the adsorbed Cr(III) had penetrated into the interior of the PNCs instead of simply adsorbing on the PNC surface. This synthesized material was found to be easily regenerated by 1.0 mol L−1p-toluene sulfonic acid (PTSA) or 1.0 mol L−1 hydrochloric acid (HCl) and efficiently reused for further Cr(VI) removal.

Carbon nanostructure-derived polyaniline metacomposites: electrical, dielectric, and giant magnetoresistive properties.

Polyaniline (PANI) nanocomposites incorporating different loadings of graphene and various other carbon nanostructures including carbon nanotubes (CNTs) and carbon nanofibers (CNFs) have been synthesized using a surface-initiated polymerization (SIP) method. Transmission electron microscopy (TEM) results indicate that the graphene has been exfoliated into a few layers (typically one, two, and three layers) during polymerization and has been uniformly dispersed in the PANI matrix. The graphene layer dispersion degree is quantified by a free-path spacing measurement (FPSM) method based on the TEM microstructures. The SIP method also demonstrates its feasibility for coating PANI on one-dimensional (1D) CNFs and CNTs without introducing additional surface functional groups. The effects of graphene size, loading level, and surface functionality on the electrical conductivity and dielectric permittivity of their corresponding nanocomposites have been systematically studied. The temperature-dependent conductivity behavior revealed a quasi-3D variable range hopping (VRH) electron transport mechanism for all the nanocomposites. Giant magnetoresistance (GMR) at room temperature is observed in pure PANI, which can be enhanced by the incorporation of a high loading of graphene (5%) due to the π-π stacking-induced efficient electron transport at the PANI/graphene interface. More interestingly, negative permittivity is found in each composite which can be easily tuned by adjusting the filler loading, morphology, and surface functionality.

Polyaniline-tungsten oxide metacomposites with tunable electronic properties†

Polyaniline (PANI) nanocomposites reinforced with tungsten oxide (WO3) nanoparticles (NPs) and nanorods (NRs) are fabricated via a facile surface-initiated-polymerization (SIP) method. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) characterizations reveal the uniform coating of polymer on the filler surface and a good dispersion of the nanofillers within the polymer matrix. Unique negative permittivity is observed in pure PANI and its nanocomposites. The switching frequency (frequency where real permittivity switches from negative to positive) can be easily tuned by changing the particle loading and filler morphology. Conductivity measurements are performed from 50∼290 K, and results show that the electron transportation in the nanocomposites follows a quasi 3-d variable range hopping (VRH) conduction mechanism. The extent of charge carrier delocalization calculated from VRH well explains the dielectric response of the metacomposites. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) reveal an enhanced thermal stability of the nanocomposites with the addition of nanofillers as compared to that of pure PANI.

Advanced micro/nanocapsules for self-healing smart anticorrosion coatings

Smart self-healing coatings for corrosion protection of metallic substrates (steel, magnesium, and aluminium, and their alloys) have attracted tremendous interest due to their capability to prevent crack propagation in the protective coatings by releasing active agents from micro/nanocapsules, that is, micro/nano particles consisting of a coating layer or a shell (micro/nanocontainers) and core material (solids, droplets of liquids or gases), in a controllable manner. This paper aims to give a concise review on the most recent advances in preparing micro/nanocapsules based on different types of micro/nanocontainers, i.e., organic polymer coatings, inorganic clays, mesoporous silica nanoparticles, polyelectrolyte multilayers, etc. for smart coatings with self-healing properties. The state-of-the-art design and preparation of micro/nanocapsules are highlighted with detailed examples.

Flame-Retardant Electrical Conductive Nanopolymers Based on Bisphenol F Epoxy Resin Reinforced with Nano Polyanilines

Both fibril and spherical polyaniline (PANI) nanostructures have successfully served as nanofillers for obtaining epoxy resin polymer nanocomposites (PNCs). The effects of nanofiller morphology and loading level on the mechanical properties, rheological behaviors, thermal stability, flame retardancy, electrical conductivity, and dielectric properties were systematically studied. The introduction of the PANI nanofillers was found to reduce the heat-release rate and to increase the char residue of epoxy resin. A reduced viscosity was observed in both types of PANI-epoxy resin liquid nanosuspension samples at lower loadings (1.0 wt % for PANI nanospheres; 1.0 and 3.0 wt % for PANI nanofibers), the viscosity was increased with further increases in the PANI loading for both morphologies. The dynamic storage and loss modulii were studied, together with the glass-transition temperature (T(g)) being obtained from the peak of tan δ. The critical PANI nanofiller loading for the modulus and T(g) was different, i.e., 1.0 wt % for the nanofibers and 5.0 wt % for the nanospheres. The percolation thresholds of the PANI nanostructures were identified with the dynamic mechanical property and electrical conductivity, and, because of the higher aspect ratio, nanofibers reached the percolation threshold at a lower loading (3.0 wt %) than the PANI nanospheres (5.0 wt %). The PANI nanofillers could increase the electrical conductivity, and, at the same loading, the epoxy nanocomposites with the PANI nanofibers showed lower volume resistivity than the nanocomposites with the PANI nanospheres, which were discussed with the contact resistance and percolation threshold. The tensile test indicated an improved tensile strength of the epoxy matrix with the introduction of the PANI nanospheres at a lower loading (1.0 wt %). Compared with pure epoxy, the elasticity modulus was increased for all the PNC samples. Moreover, further studies on the fracture surface revealed an enhanced toughness. Finally, the real permittivity was observed to increase with increasing the PANI loading, and the enhanced permittivity was analyzed by the interfacial polarization.

Polyaniline Stabilized Magnetite Nanoparticle Reinforced Epoxy Nanocomposites

Magnetic epoxy polymer nanocomposites (PNCs) reinforced with magnetite (Fe(3)O(4)) nanoparticles (NPs) have been prepared at different particle loading levels. The particle surface functionality tuned by conductive polyaniline (PANI) is achieved via a surface initiated polymerization (SIP) approach. The effects of nanoparticle loading, surface functionality, and temperature on both the viscosity and storage/loss modulus of liquid epoxy resin suspensions and the physicochemical properties of the cured solid PNCs are systematically investigated. The glass transition temperature (T(g)) of the cured epoxy filled with the functionalized NPs has shifted to the higher temperature in the dynamic mechanical analysis (DMA) compared with that of the cured pure epoxy. Enhanced mechanical properties of the cured epoxy PNCs filled with the functionalized NPs are observed in the tensile test compared with that of the cured pure epoxy and cured epoxy PNCs filled with as-received NPs. The uniform NP distribution in the cured epoxy PNCs filled with functionalized NPs is observed by scanning electron microscope (SEM). These magnetic epoxy PNCs show the good magnetic properties and can be attached by a permanent magnet. Enhanced interfacial interaction between NPs and epoxy is revealed in the fracture surface analysis. The PNCs formation mechanism is also interpreted from the comprehensive analysis based on the TGA, DSC, and FTIR in this work.