Impregnated silica nanoparticles for the reactive removal of sulphur mustard from solutions

High surface area (887.3m(2)/g) silica nanoparticles were synthesized using aerogel route and thereafter, characterized by N(2)-Brunauer-Emmet-Teller (BET), SEM and TEM techniques. The data indicated the formation of nanoparticles of silica in the size range of 24-75 nm with mesoporous characteristics. Later, these were impregnated with reactive chemicals such as N-chloro compounds, oxaziridines, polyoxometalates, etc., which have already been proven to be effective against sulphur mustard (HD). Thus, developed novel mesoporous reactive sorbents were tested for their self-decontaminating feature by conducting studies on kinetics of adsorptive removal of HD from solution. Trichloroisocyanuric acid impregnated silica nanoparticles (10%, w/w)-based system was found to be the best with least half-life value (t(1/2)=2.8 min) among prepared systems to remove and detoxify HD into nontoxic degradation products. Hydrolysis, dehydrohalogenation and oxidation reactions were found to be the route of degradation of HD over prepared sorbents. The study also inferred that 10% loading of impregnants over high surface area and low density silica nanoparticles enhances the rate of reaction kinetics and seems to be useful in the field of heterogeneous reaction kinetics.     

Ferroelastic Domain Switching in Polydomain Tetragonal Zirconia Single Crystals

As-received, yttria-doped (4.2 wt% Y₂O₃) single crystals of zirconia were heated to ≥2100°C in air. Cube-shaped samples with faces perpendicular to 〈100〉 axes on the basis of the pseudocubic symmetry were cut from the crystals. X-ray and electron diffraction indicated that the crystals are polydomain with [001] axes, on the basis of the tetragonal symmetry, in three mutually orthogonal directions (perpendicular to the cube faces). The cube-shaped crystals were tested in compression at temperatures as high as 1400°C. X-ray diffraction indicated that ferroelastic domains underwent reorientation (switching) in compression. Subsequently, notched samples with the long direction of the beams along 〈100〉 on the basis of the pseudocubic symmetry were fractured in three-point bending at temperatures as high as 1000°C. X-ray diffraction from fracture surfaces showed that domain reorientation had occurred and that no monoclinic phase was observed on fracture or ground surfaces. The fracture toughness at room temperature and at 1000°C was ∼12 and ∼8 MPa · m^1/2, respectively. Preliminary experiments on polycrystalline tetragonal zirconia samples containing 5.4 wt% Y₂O₃ and sintered at ≥2100°C also showed no evidence of the monoclinic phase on fracture or ground surfaces. The toughness of the polycrystalline samples was typically 7.7 MPa · m^1/2. These results indicate that ferroelastic domain switching can occur during fracture and may contribute to toughness.     

Physical Properties of Biodegradable Films of Soy Protein Concentrate/Gelling Agent Blends

Soy protein concentrate (SPC) is modified by blending with gelling agents such as agar, Agargel, and Phytagel and the properties of the blended films are characterized. Gelling agent addition significantly improves the mechanical properties, thermal stability, and moisture resistance. SPC blended with 30% PG show over 180% increase in the tensile stress and Young's modulus and the moisture regain decreases from 17.9 to 13.9%. The glass transition temperature of the SPC films increases from 132 to 148 °C after blending with Agargel and Phytagel. IPN‐like structure formation after adding gelling agents is responsible for the improvements. The results also suggest that the gelling agent chemistry determines the amount of gelling agent required to form IPN‐like structures.

     

Carbon nanotube/carbon nanofiber growth from industrial by-product gases on low- and high-alloy steels

The growth of carbon nanotubes (CNTs) on sheet metal surfaces (including low- and high-alloyed steel and Ni-plated steel) has been explored using a mixture of CO, CO₂, and H₂ as the precursor feedstock in a thermal chemical vapor deposition process. The influence of various experimental parameters such as the reactor temperature, reaction time, and precursor composition on the yield, purity, and dimensions of the CNTs has been elucidated. Addition of CO₂ during CNT growth leads to higher carbon deposition rates, especially for low- and high-alloyed steel. The diameters of the obtained CNTs range from 12 to 300 nm at carbon deposition rates of ～0.3 mg cm^?2 min^?1. The CNTs are observed to be uniformly distributed and adhered firmly to the substrates. The experimental conditions for CNT growth on sheet metal surfaces are very similar to concentrations and temperatures of a typical effluent stream of the steel industry. This process thus holds potential to harness waste gases to fabricate CNT-based coatings that impart added functionality to sheet metals, while further reducing the carbon footprint of steel plants.     

Structure–property correlation of polyurethane nanocomposites: Influence of loading and nature of nanosilica and microstructure of hyperbranched polyol

New generation polyurethane nanocomposites based on toluene diisocyanate, poly(propylene glycol), hyperbranched polymers (HBPs), and nanosilica were synthesized with the aim of determining the effect of the loading and nature of nanosilica and the functionality of HBP on the structure and properties of polyurethane nanocomposites. Good dispersion of nanosilica at 4 wt % loading in the polymer was confirmed from atomic force microscopy. The properties of the polyurethane nanocomposites were a function of content and nature of the nanosilica in the matrix. The optimum silica loading was 4 wt %. At this loading, tensile strength and storage modulus at 25°C of the nanocomposites increased by 52 and 40%, respectively over the pristine polyurethane. Organo‐treated nanosilica exhibited higher physico‐mechanical properties than the untreated one. With the increase of functionality in the hyperbranched polyol, the tensile strength, thermal stability, and dynamic mechanical properties of the nanocomposites improved. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Ethylene vinyl acetate/ethylene propylene diene terpolymer‐blend‐layered double hydroxide nanocomposites

Ethylene vinyl acetate (EVA‐45)/ethylene propylene diene terpolymer (EPDM) blend‐layered double hydroxide (LDH) nanocomposites have been prepared by solution blending of 1:1 weight ratio of EVA and EPDM with varying amounts of organo LDH (DS‐LDH). X‐ray diffraction and transmission electron microscopy analysis suggest the formation of partially exfoliated EVA/EPDM/DS‐LDH nanocomposites. Measurement of mechanical properties of the nanocomposites (3 wt% DS‐LDH content) show that the improvement in tensile strength and elongation at break are 35 and 12% higher than neat EVA/EPDM blends. Dynamic mechanical thermal analysis also shows that the storage modulus of the nanocomposites at glass transition temperature is higher compared to the pure blend. Such improvements in mechanical properties have been correlated in terms of fracture behavior of the nanocomposites using scanning electron microscopy analysis. Thermal stability of the prepared nanocomposites is substantially higher compared to neat EVA/EPDM blend, confirming the formation of high‐performance polymer nanocomposites. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers     

Highly transparent thermoplastic elastomer from isotactic polypropylene and styrene/ethylene‐butylene/styrene triblock copolymer: Structure‐property correlations

Polypropylene (PP) is one of the most useful general purpose plastics. However, the poor transparency and brittleness of PP restricts its applications in the field of medical and personal care where silicone and polyvinyl chloride (PVC) are presently used. This work concentrates on developing highly transparent elastomeric PP blends and also thermoplastic elastomer by blending isotactic polypropylene (I‐PP) with styrene/ethylene‐butylene/styrene (SEBS) triblock copolymer. PP/SEBS blend derived from high melt flow index (MFI) PP and high MFI SEBS exhibit remarkable transparency (haze value as low as 6%) along with good percentage of elongation and processability. The reduction in difference of refractive index (RI) between PP and SEBS has been observed by blending SEBS with PP. The wide angle X‐ray diffraction studies show that there is significant reduction in the percentage crystallinity of PP by the addition of SEBS block copolymer. Temperature‐dependent polarized light microscopy studies reveal the reduction in spherulites size by the addition of SEBS block copolymer. Transmission electron micrographs show that the SEBS polymer forms a fine lamellar structure throughout the PP matrix with phase inversion at higher SEBS concentration. Development of phase morphology, crystalline morphology, and crystallinity in different blends has been analyzed and microstructure‐haze correlations have been developed. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers     

SO2 resistant antimony promoted V2O5/TiO2 catalyst for NH3-SCR of NOx at low temperatures

To get the low temperature sulfur resistant V₂O₅/TiO₂ catalysts quantum chemical calculation study was carried out. After selecting suitable promoters (Se, Sb, Cu, S, B, Bi, Pb and P), respective metal promoted V₂O₅/TiO₂ catalysts were prepared by impregnation method and characterized by X-ray diffraction (XRD) and Brunner Emmett Teller surface area (BET-SA). Se, Sb, Cu, S promoted V₂O₅/TiO₂ catalysts showed high catalytic activity for NH₃ selective catalytic reduction (NH₃-SCR) of NO_x carried at temperatures between 150 and 400 °C. The conversion efficiency followed in the order of Se > Sb > S > V₂O₅/TiO₂ > Cu but Se was excluded because of its high vapor pressure. An optimal 2 wt% ‘Sb’ loading was found over V₂O₅/TiO₂ for maximum NO_x conversion, which also showed high resistance to SO₂ in presence of water when compared to other metal promoters. In situ electrical conductivity measurement was carried out for Sb(2%)/V₂O₅/TiO₂ and compared with commercial W(10%)V₂O₅/TiO₂ catalyst. High electrical conductivity difference (ΔG) for Sb(2%)/V₂O₅/TiO₂ catalyst with temperature was observed. SO₂ deactivation experiments were carried out for Sb(2%)/V₂O₅/TiO₂ and W(10%)/V₂O₅/TiO₂ at a temperature of 230 °C for 90 h, resulted Sb(2%)/V₂O₅/TiO₂ was efficient catalyst. BET-SA, X-ray photoelectron spectroscopy (XPS) and carbon, hydrogen, nitrogen and sulfur (CHNS) elemental analysis of spent catalysts well proved the presence of high ammonium sulfate salts over W(10%)/V₂O₅/TiO₂ than Sb(2%)/V₂O₅/TiO₂ catalyst.     

Fabrication and Properties of Ethylene Vinyl Acetate-Carbon Nanofiber Nanocomposites

Carbon nanofiber (CNF) is one of the stiffest materials produced commercially, having excellent mechanical, electrical, and thermal properties. The reinforcement of rubbery matrices by CNFs was studied in the case of ethylene vinyl acetate (EVA). The tensile strength was greatly (61%) increased, even for very low fiber content (i.e., 1.0 wt.%). The surface modification of the fiber by high energy electron beam and gamma irradiation led to better dispersion in the rubber matrix. This in turn gave rise to further improvements in mechanical and dynamic mechanical properties of EVA. The thermal conductivity also exhibited improvements from that of the neat elastomer, although thermal stability of the nanocomposites was not significantly altered by the functionalization of CNFs. Various results were well supported by the morphological analysis of the nanocomposites.     

Characterization of Soot Deposition and Particle Nucleation in Exhaust Gas Recirculation Coolers

Cooled exhaust gas recirculation (EGR) is used to control engine out NO_x (oxides of nitrogen) emissions from modern diesel engines by re-circulating a portion of the exhaust gases into the intake manifold of an engine after cooling it through a heat exchanger commonly referred to as an EGR cooler. However, EGR cooler fouling due to presence of soot particles and hydrocarbons (HC) in engine exhaust leads to a decrease in cooler efficiency and increased pressure drop across the cooler. This can adversely affect the combustion process, engine durability, and emissions. In this study, a multicylinder diesel engine was used to produce a range of engine out HC and soot concentrations to investigate soot deposition and particle nucleation in an EGR cooler. A portion of the engine exhaust was passed through an EGR cooler, while particle size and HC concentration measurements were made at the cooler inlet and outlet. Tests were conducted over a range of EGR cooler coolant temperatures and engine out soot and HC concentrations to determine the impact on the nucleation and accumulation modes of the exhaust particle size distributions. A reduction in the accumulation mode particle concentration at the EGR cooler outlet was observed for high soot concentrations indicating soot deposition within the EGR cooler. As the EGR coolant temperature was reduced, the outlet accumulation mode particle concentration was reduced further, indicating increased soot deposition in the cooler due to increased thermophoresis. There were no signs of diffusiophoresis due to HC diffusion within the cooler over the range of conditions used in the study. A significant increase in outlet nucleation mode particle concentration was observed for the low soot concentrations. This mode increased with either increasing HC concentration or decreasing coolant temperature, indicating the saturation ratio (SR) dependence of the nucleation mode formation. However, as the soot concentration was increased, the nucleation mode disappeared because of HC adsorption onto the increased soot surface area.

Copyright 2012 American Association for Aerosol Research