Using magnetic susceptibility to evaluate pollution status of the sediment for a typical reservoir in northwestern China.

Intensive anthropogenic activities may add to pollution risks to lakes and rivers, which can be revealed by the magnetic characteristics of sediments. The present study aims to assess the pollution status of the sediment of a typical reservoir in northwestern China by application of magnetic susceptibility. The values of magnetic susceptibility exhibited significant positive correlations with trace metals (Co, Cu, Mn, Ni, and V) and natural radionuclides (232Th and 40K). Multivariate statistical analysis indicated common sources and similar deposition characteristics of magnetic particles and trace metals. It was conformed that magnetic susceptibility could be used as an indicator to identify industrial sources of trace metals, but was not suitable to indicate the traffic or natural sources. Linear regression equations between the low-frequency magnetic susceptibility and the integrated pollution index as well as annual effective dose rate indicated a potential for using magnetic susceptibility in semi-quantitative assessment of trace metal pollution and radiological hazard in sediments. A three-step procedure is proposed for the use of magnetic susceptibility in pollution monitoring, which provides a fast and effective method for estimating the pollution extent and tracing the major sources of trace metals in the sediment of lakes and rivers.

[Contamination Levels and Source Analysis of Heavy Metals in the Finer Particles of Urban Road Dust from Xi'an, China].

Road dust samples were collected from four different functional areas in Xi'an City, i.e., an educational area, a residential area, a park area, and a traffic area, to study the influence of intensive human activities on local urban environmental quality. The contents of Cu, Pb, Zn, Cr, Co, V, Mn, and Ni in the smaller than 63 µm road dust particles were determined by X-ray fluorescence spectrometry, and the pollution levels of these metals were assessed by a geoaccumulation index and a pollution loading index. The possible sources of heavy metals measured in the dusts were identified by multivariate statistical analysis methods, including correlation analysis, principal component analysis, and cluster analysis, and the contributions of each source to heavy metals in the dusts were apportioned by a principal component analysis-multiple linear regression receptor model. The results showed that the contents of Cu, Pb, Zn, Cr, Co, V, Mn, and Ni in the smaller than 63 µm road dust particles of urban road dust from Xi'an ranged 14.2-96.9, 23.5-206.1, 20.0-899.4, 122.7-262.8, 7.9-14.2, 48.7-71.5, 274.0-448.9, and 22.4-62.5 mg·kg-1, respectively, with averages of 46.6, 97.4, 169.2, 177.5, 9.8, 57.1, 337.6, and 29.3 mg·kg-1. Compared to the element background values of Shaanxi soil, the finer particles of road dust from Xi'an had elevated contents of Cu, Pb, Zn, and Cr. The finer particles of road dust from Xi'an were unpolluted by Co, V, Mn, and Ni; unpolluted to moderately polluted by Cr, Cu, and Zn; and moderately polluted by Pb. The assessment results of comprehensive pollution indicated that the pollution levels of the heavy metals in the dusts were mainly unpolluted to moderately polluted. The multivariate statistical analysis results displayed that Cr, Cu, Pb, and Zn had significant positive correlation. These metals belong to a principal component and a cluster, whereas Mn, Ni, V, and Co belong to another principal component and cluster and have significant positive correlation. Considering the content characteristics of heavy metals in the dusts, these results illustrated that two kinds of sources for the heavy metals studied existed for the finer particles of road dust from Xi'an, i.e., Cu, Pb, Zn, and Cr mainly originated from traffic sources, whereas V, Co, Mn, and Ni were mainly from natural sources. The contributions of traffic sources and natural sources to the heavy metals in the finer particles of the road dust from Xi'an were respectively 56.7% and 43.3%.

Accumulation degree and source apportionment of trace metals in smaller than 63 µm road dust from the areas with different land uses: A case study of Xi'an, China.

Finer urban dusts have more serious environmental detriment and health risk than coarser urban dusts. The trace metals Pb, Cu, Zn, Cr, Co, Ba, Mn, Ni, V, Y, Rb, Ga, Hf, and Zr were analyzed using X-ray fluorescence spectrometry in smaller than 63 µm road dust collected from the areas with different land use types and human activities in Xi'an city. The purposes of this study were to reveal the impact of human activities on the environment through element enrichment factor, and to determine the sources of trace metals measured by multivariate statistical analysis and multiple liner regression of absolute principal component scores. The results indicated that the smaller than 63 µm road dust in Xi'an, in comparison to the element background value of local soil, had higher Cu, Pb, Zn, Cr, Y, Hf and Zr concentrations. Trace metals had different variations in the dusts, while the anthropogenic trace metals had no significant difference in the four areas owing to the wide existing of human activities. The accumulation level of Pb was the highest, followed by Cr, Cu and Zn, and then was Hf and Zr, while the other trace metals were deficient or deficient to minimal enrichment in the finer road dust. Source analysis results indicated that Co, Ga, Mn, Ni, V, Rb and Y mainly originated from natural source, which accounted about 57%-87% for these metals' concentration. Ba, Cr, Pb, Cu and Zn primarily derived from traffic source, which contributed approximately 59%-79% to these metals' content. Hf and Zr were mainly from construction source, which contributed 74.6% to Hf concentration and 78.2% to Zr concentration. The study indicated that traffic and construction activities had a predominant influence on local environment.

Core-Shell Co/CoO Integrated on 3D Nitrogen Doped Reduced Graphene Oxide Aerogel as an Enhanced Electrocatalyst for the Oxygen Reduction Reaction.

Here, we demonstrate that Cobalt/cobalt oxide core-shell nanoparticles integrated on nitrogen-doped (N-doped) three-dimensional reduced graphene oxide aerogel-based architecture (Co/CoO-NGA) were synthesized through a facile hydrothermal method followed by annealing treatment. The unique endurable porous structure could provide sufficient mass transfer channels and ample active sites on Co/CoO-NGA to facilitate the catalytic reaction. The synthesized Co/CoO-NGA was explored as an electrocatalyst for the oxygen reduction reaction, showing comparable oxygen reduction performance with excellent methanol resistance and better durability compared with Pt/C.

Binder-Free and Carbon-Free 3D Porous Air Electrode for Li-O2 Batteries with High Efficiency, High Capacity, and Long Life.

Pt-Gd alloy polycrystalline thin film is deposited on 3D nickel foam by pulsed laser deposition method serving as a whole binder/carbon-free air electrode, showing great catalytic activity enhancement as an efficient bifunctional catalyst for the oxygen reduction and evolution reactions in lithium oxygen batteries. The porous structure can facilitate rapid O2 and electrolyte diffusion, as well as forming a continuous conductive network throughout the whole energy conversion process. It shows a favorable cycle performance in the full discharge/charge model, owing to the high catalytic activity of the Pt-Gd alloy composite and 3D porous nickel foam structure. Specially, excellent cycling performance under capacity limited mode is also demonstrated, in which the terminal discharge voltage is higher than 2.5 V and the terminal charge voltage is lower than 3.7 V after 100 cycles at a current density of 0.1 mA cm(-2) . Therefore, this electrocatalyst is a promising bifunctional electrocatalyst for lithium oxygen batteries and this depositing high-efficient electrocatalyst on porous substrate with polycrystalline thin film by pulsed laser deposition is also a promising technique in the future lithium oxygen batteries research.

Synthesis-Dependent Surface Defects and Morphology of Hematite Nanoparticles and Their Effect on Cytotoxicity in Vitro.

In this study, we investigate the toxicity of hematite (α-Fe2O3) nanoparticles on the Madin-Darby Canine Kidney (MDCK) cell line. The oxide particles have been synthesized through two different methods and annealing conditions. These two methods, spray precipitation and precipitation, resulted in particles with rod-like and spherical morphology and feature different particle sizes, surface features, and magnetic properties. Through flow cytometry it was found that particle morphology heavily influences the degree to which the nanomaterials are internalized into the cells. It was also found that the ability of the nanoparticles to generate free radicals species is hindered by the formation of tetrahedrally coordinated maghemite-like (γ-Fe2O3) spinel defects on the surfaces of the particles. The combination of these two factors resulted in variable cytotoxic effects of the hematite nanoparticles synthesized with different conditions. This article highlights the importance on the fabrication method, materials properties, and surface characteristics on the cytotoxicity of hematite nanomaterials.

N-doped crumpled graphene derived from vapor phase deposition of PPy on graphene aerogel as an efficient oxygen reduction reaction electrocatalyst.

Nitrogen-doped crumpled graphene (NCG) is successfully synthesized via vapor phase deposition of polypyrrole onto graphene aerogel followed by thermal treatment. The NCG was explored as an electrocatalyst for the oxygen reduction reaction, showing comparable electrocatalytic performance with the commercial Pt/C in alkaline membrane exchange fuel cells because of the well-regulated nitrogen doping and the robust micro-3D crumpled porous nanostructure.

Percolation Diffusion into Self-Assembled Mesoporous Silica Microfibres.

Percolation diffusion into long (11.5 cm) self-assembled, ordered mesoporous microfibres is studied using optical transmission and laser ablation inductive coupled mass spectrometry (LA-ICP-MS). Optical transmission based diffusion studies reveal rapid penetration (<5 s, D > 80 µm²âˆ™s-¹) of Rhodamine B with very little percolation of larger molecules such as zinc tetraphenylporphyrin (ZnTPP) observed under similar loading conditions. The failure of ZnTPP to enter the microfibre was confirmed, in higher resolution, using LA-ICP-MS. In the latter case, LA-ICP-MS was used to determine the diffusion of zinc acetate dihydrate, D~3 × 10-4 nm²âˆ™s-1. The large differences between the molecules are accounted for by proposing ordered solvent and structure assisted accelerated diffusion of the Rhodamine B based on its hydrophilicity relative to the zinc compounds. The broader implications and applications for filtration, molecular sieves and a range of devices and uses are described.

PdNi hollow nanoparticles for improved electrocatalytic oxygen reduction in alkaline environments.

Palladium-nickel (PdNi) hollow nanoparticles were synthesized via a modified galvanic replacement method using Ni nanoparticles as sacrificial templates in an aqueous medium. X-ray diffraction and transmission electron microscopy show that the as-synthesized nanoparticles are alloyed nanostructures and have hollow interiors with an average particle size of 30 nm and shell thickness of 5 nm. Compared with the commercially available Pt/C or Pd/C catalysts, the synthesized PdNi/C has superior electrocatalytic performance towards the oxygen reduction reaction, which makes it a promising electrocatalyst for alkaline anion exchange membrane fuel cells and alkali-based air-batteries. The electrocatalyst is finally examined in a H2/O2 alkaline anion exchange membrane fuel cell; the results show that such electrocatalysts could work in a real fuel cell application as a more efficient catalyst than state-of-the-art commercially available Pt/C.

Structurally and electronically designed TiO2Nx nanofibers for lithium rechargeable batteries.

The morphology and electronic structure of metal oxides, including TiO(2) on the nanoscale, definitely determine their electronic or electrochemical properties, especially those relevant to application in energy devices. For this purpose, a concept for controlling the morphology and electrical conductivity in TiO(2), based on tuning by electrospinning, is proposed. We found that the 1D TiO(2) nanofibers surprisingly gave higher cyclic retention than 0D nanopowder, and nitrogen doping in the form of TiO(2)N(x) also caused further improvement. This is due to higher conductivity and faster Li(+) diffusion, as confirmed by electrochemical impedance spectra. Our findings provide an effective and scalable solution for energy storage efficiency.

Synthesis and characterization of self-assembled c-axis oriented Bi2Sr3Co2O(y) thin films by the sol-gel method.

Bi(2)Sr(3)Co(2)O(y) thin films are prepared on SrTiO(3) (100), (110) and (111) single crystal substrates using the sol-gel method. All the thin films are c-axis oriented regardless of the orientation of the substrate suggesting self-assembled c-axis orientation, and X-ray photoelectron spectroscopy results give evidence of coexistence of Co(3+) and Co(2+) ions in the derived films. Transmission electronic microscopy observations reveal that all samples are c-axis oriented with no obvious differences for different samples, and the c-axis lattice constant is determined as ~15 Å suggesting the misfit structure. A phenomenological thermodynamic phase diagram for self-assembled c-axis orientation is established for misfit cobaltate-based films using chemical solution deposition. All samples behave like semiconductors due to the coexistence of Co(3+)/Co(2+) ions, and the resistivity at 350 K is ~47, 39 and 17 mΩ cm for the thin films on SrTiO(3) (100), (110) and (111), respectively, whereas the Seebeck coefficient at 300 K is 97, 89 and 77 µV K(-1). The successful attainment of Bi(2)Sr(3)Co(2)O(y) thin films with self-assembled c-axis orientation will provide an effective prototype for investigation of growth mechanisms in complex oxide thin films with a misfit structure.