A hierarchical hybrid of ZnCo2O4 and rGO as a significant electrocatalyst for methanol oxidation reaction: Synthesis,characterization, and electrocatalytic performance

Hierarchical porous ZnCo₂O₄ nanosheets and ZnCo₂O₄-coated reduced graphene oxide (ZnCo₂O₄/rGO) were synthesized by the hydrothermal method followed by the annealing process. The composition of materials was proved by X-ray electron spectroscopy and X-ray photoelectron spectroscopy. The size and morphology of the as-prepared samples were evaluated by scanning electron microscopy and transmission electron microscopy. The result showed ZnCo₂O₄ nanosheets with porous morphology and a sheet thickness of about 5 nm was well synthesized. The electrochemical tests used to prove the catalytic performance of the prepared catalysts were cyclic voltammetry and impedance spectroscopy, and the analysis was performed in alkaline environments. The electrochemical investigations on ZnCo₂O₄ and ZnCo₂O₄/rGO showed the rGO has an effective role in electrooxidation of methanol in alkaline media. In addition to the synergic effect between Zn and Co, the synergistic effect between ZnCo₂O₄ (make active sites for adsorption of methanol) and rGO (provide more conductivity and make more sites by preventing from the agglomeration of ZnCo₂O₄) has an important role for this excellent performance. The polarization curves of ZnCo₂O₄/rGO showed a maximum power density of 24.3 mW cm⁻², which proved its potential capability for the direct methanol fuel cell.     

Grafting of water‐soluble sulfonated monomers onto functionalized fumed silica nanoparticles via surface‐initiated redox polymerization in aqueous medium

Sulfonated polymer/fumed silica hybrid nanoparticles were prepared via surface‐initiated free radical polymerization of 2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid (PAMPS‐g‐FSN), styrene sulfonic acid sodium salt (PSSA‐g‐FSN) and vinyl sulfonic acid sodium salt (PVSA‐g‐FSN) from the surface of aminopropyl‐functionalized fumed silica nanoparticles (AFSNs) dispersed in aqueous medium. Cerium(IV) ammonium nitrate/nitric acid and sodium dodecyl sulfate were used as redox initiator and stabilizer respectively. AFSNs were prepared by covalently attaching 3‐aminopropyltriethoxysilane onto the surface of fumed silica nanoparticles. Sulfonated monomers (AMPS, SSA or VSA) were then grafted onto the AFSNs ultrasonically dispersed in water via redox initiation at 40 °C. Structure, thermal properties, particle size and morphology of the AFSNs and PAMPS‐g‐FSN, PSSA‐g‐FSN and PVSA‐g‐FSN hybrid nanoparticles were characterized by Fourier transform infrared spectroscopy, TGA, SEM, transmission electron microscopy (TEM) and dynamic light scattering (DLS). The results indicated that the sulfonated monomers were successfully grafted onto the fumed silica nanoparticles. Grafting amounts of the sulfonated polymers onto the fumed silica nanoparticle surface were estimated from TGA thermograms to be 59%, 13% and 29% for the PAMPS, PSSA and PVSA, respectively. From SEM, TEM and DLS analysis, polymer‐grafted fumed silica nanoparticles with an average diameter smaller than 70 nm and a (semi‐) spherical shape were observed. A significant bimodal particle size distribution was observed only for the PAMPS‐g‐FSN with average diameters of 39.6 nm (84.1% per number) and 106 nm (15.9% per number). The hydrophilic sulfonated polymer/grafted fumed silica obtained from the redox graft polymerization gave a stable colloidal dispersion in acidic aqueous medium. Copyright © 2012 Society of Chemical Industry     

Novel design of a RF-MEMS tuneable capacitor based on electrostatically induced torsion

Micro-Electro-Mechanical System (MEMS) RF switches have been one of the most interesting areas for research and development in the last years. It has been shown that they have an excellent performance in the RF and microwave frequency range and a great effort has been dedicated in designing suitable geometries and structures best suited for switching application. In parallel other devices useful for the construction of complex RF circuits have been proposed and studied. Among these tuneable capacitors are of high interest for a variety of applications. In this paper we present a new electromechanical design for a tuneable capacitor with a totally different shape from usual designs. In particular we try to exploit the effect of the small in-plane force that develops during the polarization of a parallel plate capacitor with partially overlapping plates. First prototype realizations aiming at the development of the electromechanic aspects of the concept are discussed and analyzed and as the first realization showed some problems an improved design is presented.     

Modification of silica nanoparticles with hydrophilic sulfonated polymers by using surface-initiated redox polymerization

Sulfonated polymer/silica hybrid nanoparticles were prepared by free radical polymerization of 2-acrylamido-2-methyl-1-propane sulfonic acid (PAMPS-g-SN) and styrene sulfonic acid sodium salt (PSSA-g-SN), initiated on the surfaces of aminopropyl-functionalized silica nanoparticles (ASN). Ce(IV) ammonium nitrate/nitric acid and sodium dodecyl sulfate were used as redox initiator and stabilizer, respectively. ASN Nanoparticles were synthesized by a covalently attached 3-aminopropyltriethoxysilane onto the surface of silica nanoparticles. Sulfonated monomers (AMPS or SSA) were then grafted onto the ASN nanoparticles, ultrasonically dispersed in water, using redox initiator system at 40?°C. ASN, PAMPS-g-SN and PSSA-g-SN nanoparticles were characterized by Fourier transform infrared (FTIR), thermogravimetry, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. FTIR and TGA results indicated that both AMPS and SSA monomers were successfully grafted onto the silica nanoparticles. The grafted amounts of sulfonated polymers onto the silica nanoparticles were estimated from TGA thermograms to be 46 and 22?% for PAMPS and PSSA, respectively. From SEM and TEM micrographs, the average-diameters of the polymer-grafted silica nanoparticles were measured to be <50?nm with a (semi)spherical morphology, in which several silica nanoparticles were able to form a core with PAMPS or PSSA existing around the silica nanoparticles.     

Dye Adsorption on Cubic Polyhedral Oligomeric Silsesquioxane-Based Poly(acrylamide-<Emphasis Type="Italic">co</Emphasis>-itaconic acid) Hybrid Nanocomposites: Kinetic,Thermodynamic and Isotherms Studies

In the present study, poly(acrylamide-co-itaconic acid) hybrid nanocomposites were synthesized via free radical copolymerization method. Octavinyl polyhedral oligomeric silsesquioxane (OV-POSS) with different weight ratio (0, 4, 8, 12 and 14 wt%) was utilized as a cross-linker. Dye adsorption properties of the as-prepared hybrid nanocomposites were investigated for crystal violet (CV) elimination from aqueous solution. The effect of various parameters, such as OV-POSS content, adsorbent amount, pH, temperature, contact time and initial dye concentration, on the adsorption of CV was studied. Moreover, adsorption kinetic, isotherm and the thermodynamic of the CV adsorption on the so-called hybrid nanocomposites were studied.     

Preparation of hydrophilic dimethyl 5‐sodium sulfoisophthalate/poly(ethylene terephthalate) nanofiber composite membranes for improving antifouling properties

In this study, the effect of dimethyl 5‐sodium sulfoisophthalate (SSI) nanoparticles (NPs) on the antifouling properties of poly(ethylene terephthalate) (PET) electrospun nanofiber membranes (ENMs) was investigated through the ultrafiltration of C. I. Basic Blue 3. 3 dye. To reveal the tortuous effect of this additive on the antifouling properties, scanning electron microscopy was used for the characterization of the ENM structure and the optimization of the SSI NP content. Then, some selected physical and structural properties of the membrane, such as the porosity, moisture regain, contact angle, hydraulic permeability (L _p ), and mechanical properties, in the optimized range of SSI NP contents were investigated. Finally, the influence of this additive on the rejection and flux recovery ratio of the prepared membranes was considered. Consequently, the antifouling properties were assessed with consideration of all of the aforementioned parameters. The SSI/PET2 membrane (that with 0.02% w/w SSI NPs with respect to the total amount of PET polymer and SSI NPs), with an average nanofiber diameter of 450 nm, a porosity of 78.44%, a moisture regain of 9.34%, a contact angle of 86.48°, an L _p of 42,167 L h^?1 m^?2 bar^?1, a tensile strength of 4.66 ± 0.04 MPa, a flux recovery ratio of 15.3%, and a final rejection of 95%, showed a significant enhancement in the antifouling properties compared with pristine PET ENMs. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44522.