Henry A. Colorado

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.

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.

Epoxy resin nanosuspensions and reinforced nanocomposites from polyaniline stabilized multi-walled carbon nanotubes

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 (Tg) 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.

Mesoporous magnetic carbon nanocomposite fabrics for highly efficient Cr(VI) removal

We have demonstrated that magnetic carbon nanocomposite fabrics prepared by microwave assisted heating are advanced adsorbents in the removal of Cr(VI) with a much higher removal capacity of 3.74 mg g−1 compared to 0.32 mg g−1 for cotton fabrics and 0.46 mg g−1 for carbon fabrics. The enhanced Cr(VI) removal is attributed to the highly porous structure of the nanocomposites. The adsorption kinetics follow the pseudo-second-order model, which reveals a very large adsorption capacity and high adsorption rate. The removal process takes only 10 min, which is much faster than conventional adsorbents such as activated carbon and biomass that often requires hours of operation. The significantly reduced treatment time and the large adsorption capacity make these nanocomposite fabrics promising for the highly efficient removal of heavy metals from polluted water.

Magnetic field induced capacitance enhancement in graphene and magnetic graphene nanocomposites

Magnetic graphene nanocomposites (MGNCs) synthesized by a facile thermal decomposition method have been introduced. TEM observations reveal a uniform distribution of the Fe2O3 nanoparticle size and preferential nuclei growth along the edge defects. Both graphene and its Fe2O3 nanocomposites are prepared as electrochemical electrodes to evaluate their capacitor performances. Under normal conditions (without a magnetic field), the MGNCs show lower capacitance than graphene due to the large particle loading (52.5 wt%), which brings larger internal resistance and thus prevents efficient electron transportation within the electrodes. However, in the presence of an external magnetic field, both graphene and MGNC electrodes exhibit significantly enhanced capacitance as compared to the results obtained under normal conditions. Specifically, the capacitance of graphene is increased by 67.1 and 26.8% at the sweeping rates of 2 and 10 mV s−1, respectively. Even larger enhancements of 154.6 and 98.2% were observed in MGNCs at the same sweeping rates of 2 and 10 mV s−1, respectively. The energy density and power density of the electroactive materials are also dramatically enhanced in the presence of a magnetic field. Equivalent circuit modeling of impedance spectra revealed that the magnetic field played a critical role in restricting the interfacial relaxation process and thus enhanced the electrode capacitance. These findings present a potential revolution of traditional electrochemical capacitors by simply applying an external magnetic field to enhance the capacitance dramatically (even doubling it depending on the electroactive materials) without material replacement and structural modification.

Polypyrrole doped epoxy resin nanocomposites with enhanced mechanical properties and reduced flammability

For the liquid epoxy nanosuspensions with both fibril and spherical polypyrrole (PPy) nanostructures, a stronger PPy nanofibers/epoxy interaction and more temperature stable behavior with a lower flow activation energy of nanosuspensions with nanofibers (54.34 kJ mol−1) than that with nanospheres (71.15 kJ mol−1) were revealed by rheological studies. As well as the common enhancing mechanism of limiting crack propagation in the polymer matrix, the nanofibers further initiated the shear bands in the epoxy resin to give a higher tensile strength (90.36 MPa) than that of pure epoxy (70.03 MPa) and even that of the epoxy nanocomposites with nanospheres (84.53 MPa). With a larger specific surface area, the nanofibers rather than nanospheres were observed to reduce the flammability of epoxy more efficiently by assisting more char formation of the epoxy resin. The hydroxyl groups formed between the protons of the doped acid in the PPy nanofillers and the epoxy broke the conjugate structure of PPy, leading to a higher bandgap in the nanocomposites (Eg1 = 3.08 eV for 1.0 wt% PPy nanofibers) than that of pure nanofillers (1.8 eV for PPy nanofibers and 1.2 eV for PPy nanospheres). Due to the high aspect ratio, the PPy nanofibers could form the conductive path more easily than the PPy nanospheres to provide a lower percolation threshold value. The real permittivity was observed to increase with increasing the PPy nanofiller loading, and the enhanced permittivity was interpreted by the interfacial polarization.

Iron-core carbon-shell nanoparticles reinforced electrically conductive magnetic epoxy resin nanocomposites with reduced flammability

Carbon coated iron (Fe@C) nanoparticles successfully served as nanofillers for obtaining magnetic epoxy resin polymer nanocomposites (PNCs). The effects of nanofiller loading level on the rheological behaviors, thermal stability, flammability, dynamic mechanical, mechanical properties, electrical conductivity and magnetic properties were systematically studied. And the curing process of the PNCs was also studied by Fourier transform infrared spectroscopy test. A reduced viscosity was observed in the 1.0 wt% Fe@C/epoxy resin liquid suspension samples and the viscosity was increased with further increasing the Fe@C nanoparticle loading. In the TGA test, the introduction of the Fe@C nanofillers gave a lower onset decomposition temperature of the PNCs. However, a reduced flammability was observed in the PNCs due to the easier char formation from epoxy matrix induced by the Fe@C nanoparticles. The dynamic storage and loss modulii were studied together with the glass transition temperature (Tg) being obtained from the peak of tanδ. Enhanced storage modulus was observed in the PNCs with 20.0 wt% Fe@C nanoparticles. The percolation thresholds of the Fe@C nanoparticles were identified with the study of tensile strength and electrical conductivity. Due to the cavities initiated by the nanoparticles, the PNCs with 5.0 wt% Fe@C nanoparticles showed an increased tensile strength up to 60% compared with pure epoxy. The Fe@C nanofillers could efficiently increase the electrical conductivity of the epoxy matrix, and the particle chain observed in the SEM image of fracture surface indicated the formation of percolated Fe@C nanoparticles in the epoxy matrix. Finally, the Fe@C nanoparticles become magnetically harder after dispersing in epoxy due to the decreased interparticle dipolar interaction, which arises from the enlarged nanoparticle spacer distance for the single domain nanoparticles.

Magnetic graphene oxide nanocomposites: nanoparticles growth mechanism and property analysis

The growth mechanism of magnetic nanoparticles (NPs) in the presence of graphite oxide (GO) has been investigated by varying the iron precursor dosage and reaction time (product donated as MP/GO). The synthesized magnetic NPs were anchored on the GO sheets due to the abundant oxygen-containing functionalities on the GO sheets such as carboxyl, hydroxyl and epoxy functional groups. The introduced NPs changed the intrinsic functionalities and lattice structure of the basal GO as indicated by FT-IR, Raman and XRD analysis, and this effect was enhanced by increasing the amount of iron precursor. Uniform distribution of NPs within the basal GO sheets and an increased particle size from 19.5 to 25.4, 31.5 and 85.4 nm were observed using scanning electron microscope (SEM) and transmission electron microscope (TEM) when increasing the weight ratio of GO to iron precursor from 10:1, to 5:1, 1:1 and 1:5, respectively. An aggregation of NPs was observed when increasing the iron precursor dosage or prolonging the reaction time from 1 to 8 h. Most functionalities were removed and the magnetic NPs were partially converted to iron upon thermal treatment under a reducing condition. The GO and MP/GO nanocomposites reacted for one and two hours (denoted as MP/GO1-1 h and MP/GO1-2 h) were converted from insulator to semiconductor after the annealing treatment as annealed GO (A-GO, 8.86 S cm−1), annealed MP/GO1-1 h (A-MP/GO1-1 h, 7.48 × 10−2 S cm−1) and annealed MP/GO1-2 h (A-MP/GO1-2 h, 7.58 × 10−2 S cm−1). The saturation magnetization was also enhanced significantly after the annealing treatment, increased from almost 0 to 26.7 and 83.6 emu g−1 for A-MP/GO1-1 h and A-MP/GO1-2 h, respectively.

Pultruded glass fiber- and pultruded carbon fiber-reinforced chemically bonded phosphate ceramics

The main goal of this article is to present the pultrusion process for glass fiber- and carbon fiber-reinforced chemically bonded phosphate ceramics (CBPCs). Samples were fabricated with 15% of fibers by volume. An improvement (with respect to the matrix) of 29 times for the bending strength of CBPCs pultruded graphite fibers composites and 17 times for CBPCs pultruded glass fiber composites is shown. Bending strength was obtained with the three-point bending test. The CBPCs were fabricated by mixing special formulations of both wollastonite powder and phosphoric acid, through resonant acoustic mixing. The microstructure was analyzed with optical and scanning electron microscopes. X-ray compositional maps were obtained for the cross-section of pultruded samples with SEM-EDS. Pultruded sample response at high temperature and thermal shock were also analyzed. The structural characterization of samples was conducted by using X-ray micro tomography.