Enhanced airborne polychlorinated biphenyl (PCB) concentrations and chlorination downwind of Lake Ontario

Air samples were collected simultaneously at three sites downwind of Lake Ontario and at a control site near Lake Erie from March to July of 1999. The Lake Erie site (Stockton, NY) had PCB concentrations similar to rural Integrated Atmospheric Deposition Network (IADN) sampling sites across the Great Lakes, exhibited limited seasonal variation, and approximates regional background. Samples taken along Lake Ontario's southeastern shore (Rice Creek and Sterling, NY) had elevated PCB concentrations averaging approximately 1 ng/m3 and were more chlorinated than air collected at IADN sites and at Stockton. Air samples from Potsdam (approximately 75 km inland) had similar concentrations but were less chlorinated. Clausius-Clapeyron plots revealed a strong correlation between PCB fugacity and temperature near Lake Ontario; however, the extent of chlorination of the air samples rules out volatilization from the lake as a major source. It is hypothesized that volatilization from local surfaces, enriched in higher chlorinated congeners by meteorological or geographic factors, drives both the concentration and composition of airborne PCBs along Lake Ontario's southeastern shore.     

Yam affects the antioxidative and gel‐forming properties of surimi gels

The antioxidative activities and textural properties of pollock surimi gels containing four different yams were determined to evaluate the potential of using yam as a health ingredient and an alternative source for starch in surimi‐based seafoods. Surimi gels containing 20% fresh yam showed higher α,α‐diphenyl‐β‐pricryl‐hydrazyl (DPPH) radicals scavenging activities and total phenolic contents than the gels without yam. Two tested cultivars, 70W34 and 70W35, did not show significant reductions in antioxidative activities when used in surimi gel while three other cultivars revealed species‐dependant declines in both the DPPH scavenging activities and total phenolic contents. The surimi gel containing the cultivar 70R20 showed the highest breaking forces and deformations. In general, 20% fresh yam could be used to form a yam‐containing surimi gel having similar textural properties with a potato starch containing pollock surimi gel. The dried yam powders might be used at the amount of 30% fresh yam equivalent without causing significant losses of the textural properties of pollock surimi gels. Copyright © 2005 Society of Chemical Industry     

Solid oxide fuel cells with YSZ-BNO Bi-layer electrolyte film deposited by magnetron sputtering

Bi-layer electrolyte films of Zr_0.84Y_0.16O_1.92 (YSZ)- 0.79Bi₂O₃-0.21Nb₂O₅ (BNO) were deposited by RF magnetron sputtering on NiO-SDC anode substrates. The stoichiometry of the BNO electrolyte film was found strongly dependent on the ratio of Ar and O₂ during sputtering, and the BNO film deposited at a mixture of 31 sccm Ar and 7 sccm O₂ appeared to be the closest to the target composition. When deposited at 300 °C and subsequently annealed at 700 °C, the BNO electrolyte emerged to be crack free and dense with some scattering closed pores. The XRD patterns of the film are indexed to the cubic Fm m structure of Bi₃NbO₇. The as-deposited film was well-crystalline and consisted of fine grains and random orientation microstructures. For electrolyte thicknesses of approximately 4.0 μm YSZ and 1.5 μm BNO layers, the open circuit voltage (OCV) and the maximum power density of the single cell with Ag cathode read respectively 0.94 V and 10 mW/cm² at 600 °C. These OCV values are lower than the expected theoretical value due to the high partial electronic conductivity.     

How to manipulate the electrospinning jet with controlled properties to obtain uniform fibers with the smallest diameter?—a brief discussion of solution electrospinning process

Solutions of five different polymers, namely, polystyrene (PS), polyacrylonitrile (PAN), polyhydroxybutrate (PHB), poly(D-L-lactic acid) (PLA), and Nylon6, were used to investigate their rheological properties on the electrospinnability. In order to effectively reduce the diameter of electrospun fibers, polymers with higher molecular weights (MW) were needed to develop entangled solutions at much lower concentrations and with viscosities as low as that of a pure solvent. A minimum polymer concentration 1.0–2.0 times larger than the entanglement concentration was required to prepare the bead-free fibers. Using this strategy, uniform PS fibers with the lowest ever diameter of ∼15 nm were successfully obtained using an MW of 3 × 10⁷ g/mol at a concentration of 0.1 vol.%. For a given electrospinning solution, processing variables of low flow-rate (Q) and high voltage (V) were desirable in obtaining fibers with small diameters. However, Q and V were correlated by a power law relation: V∼Q ^a, wherein the exponent a had a value of 0.1–0.4, which was relevant with the solution types. Based on the finite element analysis (FEA), a significant measure of electric field (E) occurred around the needle tip used in the experiment, and its magnitude decayed with increasing distance from the needle end (z): E∼z ⁻ⁿ. The exponent n was 1.0–2.0, depending on the needle–plate geometry, i.e., needle length, needle diameter (D _o ), plate diameter, and tip-to-plate distance (H). According to FEA results, H exhibited negligible effects on the electric field in the region of interest, i.e., z/D _o ∼1 to 10. Due to the presence of high measures of E at the needle end, approaches to render a shorter and thinner straight jet issuing from the Taylor cone to yield thinner fibers were sought because a more significant jet stretching in the “jet whipping region” can take place. A feasible route to predict the as-spun fiber diameter produced by the manipulation of the electrified jet is provided by experimentally measuring the jet diameter and numerically calculating the electric field for the jet whipping process.     

Anti-UVC Irradiation and Metal Chelation Properties of 6-Benzoyl-5,7-dihydroxy-4-phenyl-chromen-2-one: An Implications for Anti-Cataract Agent

Coumarin derivative 1, 5,7-dihydroxy-6-(3-methyl-1-butyryl)-4-phenyl-chromen- 2-one, has been reported to possess radical scavenging activity and DNA protection. We have synthesized a series of coumarins with structural modifications at positions C4, C5, C6 and C7 and evaluated them for their anti-UVC properties. Coumarin 7, 6-benzoyl-5,6-dihydroxy-4-phenyl-chromen-2-one, was found to have the most potent activity in protecting porcine γ-crystallin against UVC insults. Results of fluorescence assays indicated that compound 7 was capable of decreasing the loss of intensity while lens crystallins and DNA PUC19 were irradiated with UVC. Presence of compound 7 decreased hydroxyl radical levels determined by probe 1b and the free iron concentrations determined by Ferrozine reagent. The chelation assay showed that compound 7 was chelated to metal via 6-CO and 5-OH on the benzopyrone ring. The observed protective effects of compound 7 towards crystallins from insults of UVC and free radicals may be due to its iron-chelating activity and its peak absorption at 254 nm.     

P–N junction mechanism on improved NiO/TiO2 photocatalyst

The composite photocatalyst comprising p-type NiO and n-type TiO₂ showed improved photoactivity due to the inhibition of electron–hole recombination. A series of P–N junction photocatalysts, NiO/TiO₂, were prepared by incipient wetness impregnation. The photocatalysts were characterized by UV–vis spectroscopy, XRD and XPS. The photoactivity of photocatalysts was tested by the degradation of methylene blue. The results showed that 0.5 wt.% NiO/TiO₂ had the highest activity as compared with TiO₂. A P–N junction mechanism was proposed and verified that the photocurrent could be enhanced under forward bias in the NiO/TiO₂ film. The photoactivity enhancement is attributed to P–N junction and co-catalyst effects.     

Electrophoretic deposition of TiO2 film on titanium foil for a flexible dye-sensitized solar cell

Electrophoretic deposition (EPD) method is employed to obtain mesoporous TiO₂ film on a titanium (Ti) foil; the film is then mechanically compressed and sintered at 350 °C before being subjected to dyeing. A comprehensive study was made on the mechanistic aspects of the EPD process. The dye-sensitized solar cell (DSSC) using the thus formed TiO₂ film rendered a power conversion efficiency (Eff.) of 6.5%. Effects of various compression pressures on the photovoltaic parameters and on other characteristic parameters of the pertinent DSSCs are studied. Electrochemical impedance spectroscopy (EIS) is applied for the first time, using a novel equivalent model, to study the impedance behavior of the DSSC with this type of TiO₂ film. We also obtain characteristic parameters of the TiO₂ photoanode by using EIS. The coordination number of the TiO₂ film, and the ratio of charge transfer resistances of electron recombination and electron transport are also obtained and analyzed. Moreover, we employ a multilayer approach and increase the film thickness to prepare TiO₂ films with the same coordination number and porosity; DSSCs using such TiO₂ films obtained from P90 and P25 rendered efficiencies of 6.5% and 5.24%, respectively. Scanning electron microscopy (SEM) micrographs are obtained to characterize the TiO₂ films formed by the EPD technique and laser-induced transient technique is used to estimate the electron lifetime in the TiO₂ films.     

Enhanced high-temperature polymer electrolyte membrane for fuel cells based on polybenzimidazole and ionic liquids

Polybenzimidazole (PBI)/ionic liquid (IL) composite membranes were prepared from an organosoluble, fluorine-containing PBI with ionic liquid, 1-hexyl-3-methylimidazolium tri?uoromethanesulfonate (HMI-Tf). PBI/HMI-Tf composite membranes with different HMI-Tf concentrations have been prepared. The ionic conductivity of the PBI/HMI-Tf composite membranes increased with both the temperature and the HMI-Tf content. The composite membranes achieve high ionic conductivity (1.6 × 10⁻² S/cm) at 250 °C under anhydrous conditions. Although the addition of HMI-Tf resulted in a slight decrease in the methanol barrier ability and mechanical properties of the PBI membranes, the PBI/HMI-Tf composite membranes have demonstrated high thermal stability up to 300 °C, which is attractive for high-temperature (>200 °C) polymer electrolyte membrane fuel cells.     

Effect of silanes on the morphology,hydrophobicity, and dynamical mechanical properties of polyimide/silica hybrid membranes

Polyimide (PI)/silica hybrid membranes with high contact angles were prepared through the in situ sol–gel process. The precursor, poly(amic acid) with controlled block chain length, was synthesized using 4,4′‐diaminodiphenyl ether (ODA), 3,3′,4,4′‐benzophenone‐tetracarboxylic dianhydride (BTDA) and 3‐aminopropyl‐trimethoxysilane (APrTMOS) or 3‐aminopropyldimethylethoxysilane (APDiMOS). And then, phenyltrimethoxysilane (PTS) or tetramethoxysilane (TMOS) or methyltrimethoxysilane (MTrMOS) was respectively, added to the above polyamic acid and mixed thoroughly. Following curing reaction, the PI/silica hybrid membranes with different cross‐linkages, silica content, and hydrophobic properties were prepared. The effect on the formation of PI imide ring during imidization reaction is increased as the increase of silanes content and characterized by frequency shiftment and absorbance ratio of Fourier transform infrared (FTIR) measurements. All the hybrid membranes show high transparency though with high silica contents. The storage modulus, tan δ, and damping intensity by DMA measurements are all correlated with silane content or block chain length. And all these membranes with silane content possess high contact angle as compared to pure PI without any silanes added and the contact angles increase with increasing the silane content. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011