Yuwen Ni

Porous nanosheet-based ZnO microspheres for the construction of direct electrochemical biosensors.

Nanosheet-based ZnO microsphere with porous nanostructures was synthesized by a facile chemical bath deposition method followed by thermal treatment, which was explored for the construction of electrochemical biosensors. Spectroscopic and electrochemical researches revealed the ZnO-based composite was a biocompatible immobilization matrix for enzymes with good enzymatic stability and bioactivity. With advantages of nanostructured inorganic-organic hybrid materials, a pair of stable and well-defined quasi-reversible redox peaks of hemoglobin was obtained with a formal potential of -0.345 V (vs. Ag/AgCl) in pH 7.0 buffer. Facilitated direct electron transfer of the metalloenzymes with an apparent heterogeneous electron transfer rate constant (k(s)) of 3.2s(-1) was achieved on the ZnO-based enzyme electrode. Comparative studies demonstrated the nanosheet-based ZnO microspheres were more effective in facilitating the electron transfer of immobilized enzyme than solid ZnO microspheres, which may result from the unique nanostructures and larger surface area of the porous ZnO. The prepared biosensor displayed good performance for the detection of H(2)O(2) and NaNO(2) with a wide linear range of 1-410 and 10-2700 microM, respectively. The entrapped hemoglobin exhibits high peroxidase-like activity for the catalytic reduction of H(2)O(2) with an apparent Michaelis-Menten constant (K(M)(app)) of 143 microM. The nanosheet-based ZnO could be a promising matrix for the fabrication of direct electrochemical biosensors, and may find wide potential applications in biomedical detection and environmental analysis.

Emissions of PCDD/Fs from municipal solid waste incinerators in China

Gas emission of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) from 19 commercial municipal solid waste (MSW) incinerators in China are investigated. The emission concentrations of PCDD/Fs were 0.042-2.461 ng TEQ Nm(-3) with an average value of 0.423 ng TEQ Nm(-3). The emissions of PCDD/Fs from 16 MSW incinerators were below the MEP regulation level (1.0 ng I-TEQ Nm(-3)), while only six systems have the dioxin emission levels below the limit established by the European Union Directive of 0.1 ng I-TEQ Nm(-3). The emission factors of PCDD/Fs from 19 MSW incinerators were calculated to be 0.169-10.72 microg TEQ ton(-1) MSW with an average value of 1.728 microg I-TEQ ton(-1) MSW. The total amount of PCDD/Fs emitted from MSW incinerators to the atmosphere in China was estimated to 19.64 g TEQ year(-1) in 2006.

Polybrominated diphenyl ethers in sediments of the Daliao River Estuary, China: levels, distribution and their influencing factors.

The concentrations, compositional profiles, possible sources of polybrominated diphenyl ethers (PBDEs) in sediments of the Daliao River Estuary as well as the factors influencing the distribution of PBDEs were investigated. The total concentrations of PBDEs ranged from 0.13 to 1.98 ng g(-1)d.w. BDE209 was the dominating congener in all sediment samples, indicating the pollution of PBDEs in the Daliao River Estuary mainly came from the use of deca-BDE commercial mixtures. The intrusion of sea waters promoted the deposition of the colloid-associated PBDEs in the estuary. There were significantly negative correlations between PBDE concentration in sediment with pH value and salinity in the bottom water. The higher river flow in the flood season (summer) obviously accelerated the transport of PBDEs, and thereby increased the risk of PBDE contamination to the deep ocean. Moreover, a positive correlation between TOC and PBDE distributions was observed, suggesting that TOC regulated the distributions of PBDEs in sediments of Daliao River Estuary.

The responses of Arabidopsis thaliana to cadmium exposure explored via metabolite profiling.

The metabolic responses of Arabidopsis thaliana to cadmium exposure was characterized in this study. A. thaliana was cultivated in medium contaminated with different cadmium concentrations (0, 5 and 50microM, respectively) for 2weeks. Metabolite analyses were performed using gas chromatography-mass spectrometry. More than 80 metabolites characterized by retention time indices and specific mass fragments were identified. The levels of carbohydrates, organic acids, amino acids, and other stress-responsive metabolites changed under cadmium stress. Treated plants showed increased levels of Ala, beta-ala, Pro, Ser, putrescine, Suc and other metabolites with compatible solute-like properties, notably 4-aminobutyric acid, glycerol, raffinose and trehalose, compared to control (untreated) plants. Studies indicated that concentrations of antioxidants (alfa-tocopherol, campesterol, beta-sitosterol and isoflavone) also increased significantly. These results confirm the important role of antioxidant defences in the mechanisms of plant-resistance to cadmium stress. Our results suggested that metabolic profiling is a powerful tool that can rapidly classify environmentally modified plants and simplify the process of cadmium-stress responses. These data will be helpful for better understanding of mechanisms of plant adaptation to cadmium stress at the metabolite level.

Stack gas emissions of PCDD/Fs from hospital waste incinerators in China.

Stack gas samples from 14 domestic-made hospital waste incinerators (HWIs) in China were collected and analyzed for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). The waste burning capacities of the investigated HWIs ranged from 5 to 25 ton d(-1). The stack gas emissions of PCDD/Fs from HWIs exhibited a large variation (0.08-31.60 ng I-TEQNm(-3)). Nine incinerators had the emission levels below the current emission standard in China (0.5 ng I-TEQN m(-3)), while only two facilities exhibited emission levels below the European Union directive emission limit (0.1 ng I-TEQN m(-3)). For two plants, concentrations of PCDD/Fs in stack gas were above 10.0 ng I-TEQN m(-3). The emission factors of PCDD/Fs from the investigated HWIs were in the range of 0.78-473.97 microg I-TEQ ton(-1) medical wastes. It was estimated that 4.87 g I-TEQ of PCDD/Fs was annually released from HWIs to the atmosphere in China in 2006. Principal component analysis and hierarchical cluster analysis were applied to analyze the congener profiles of PCDD/Fs from HWIs in China.

A promising electrochemical biosensing platform based on graphitized ordered mesoporous carbon

Three dimensional ordered graphitized mesoporous carbon GMC-6 (pore diameter ∼6 nm) and GMC-13 (pore diameter ∼13 nm), prepared by a nickel-catalyzed template-assisted method, were explored systematically for the construction of enzyme-based electrochemical biosensors. Comparative studies revealed that GMC-6 offer significant advantages over GMC-13 and graphitized multiwalled carbon nanotubes (CNTs) in facilitating the direct electron transfer of entrapped hemoglobin and improving the performance of fabricated biosensors. The possible factors that affect the biosensing performance of these carbon materials were evaluated comprehensively and comparatively based on the characterization of their physical parameters. The biosensor based on GMC-6 displayed excellent analytical performance over a wide linear range along with good stability and selectivity for the detection of hydrogen peroxide. The “entrapment” immobilization mode and “interspace confinement effect” (by restraining the unfolding or conformational change of enzyme molecules from inactivation) provided by GMC can result in pore-size-dependent enzymatic stability and bioactivity, which might be a crucial factor for the superior biosensing performance of GMC-6 to that of CNTs and GMC-13. Graphitized ordered mesoporous carbons with good pore size matching for enzymes proved to be a promising electrochemical biosensing platform.

Polychlorinated dibenzo-p-dioxins and dibenzofurans in soils and sediments from Daliao River Basin, China

Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/F) were analyzed in surface sediments and top soils collected from 30 sites in Daliao River Basin. The concentrations of PCDD/F ranged from 0.28 to 29.01 ng TEQ kg(-1) dw (mean value, 7.45 ng TEQ kg(-1)dw) in sediments, and from 0.31 to 53.05 ng TEQ kg(-1)dw (mean value, 7.00 ng TEQ kg(-1)dw) in soils. PCDD/F pollution in sediments from the mid- and downstream sections of Hun River was found to be relatively heavy, and the levels of PCDD/F contamination in paddy soils were generally higher than those of upland soils. Using multivariate statistical analysis, the PCDD/F homologue and congener profiles of all soil and sediment samples were compared with those of suspected PCDD/F sources. The results showed that, PCDD/F contamination in most sediments of Hun River should mainly originated from the production of organochlorine chemicals, while metal smelting was the important potential source of PCDD/F in the drainage area of Taizi River. PCDD/F contamination in paddy soils should be simultaneously attributed to the polluted water irrigation and the organochlorine pesticide application.

Destruction of Polychlorinated Aromatic Compounds by Spinel-Type Complex Oxides

Destruction of polychlorinated aromatic compounds was carried out over spinel-type catalysts XY2O4 (where X = Mg, Ca, Cu, Ni, Zn, and Y = Al, Fe). The catalysts were characterized by XRD, nitrogen adsorption-desorption isotherms and FTIR. The performance of these catalysts toward the decomposition of hexachlorobenzene (HCB) and octachlorodibenzo-p-dioxin (OCDD) was evaluated in a closed system. The spinel-type catalyst with mesoporous structure demonstrated high catalytic activity for the hydrodechlorination of polychlorinated aromatic compounds. Among them, the copper-aluminum spinel (CuAl2O4), specifically calcined at 600 degrees C, exhibited the best activity. More than 85% dechlorination efficiency of HCB and 99% decomposition of polychlorinated dibenzodioxin (PCDD) were achieved at 250 degrees C for 30 min over the above catalyst which was more effective than the corresponding metallic copper and copper oxide catalysts during the thermal degradation of polychlorinated aromatic compounds. The correlation of catalytic performance to structural characteristics is discussed based on the detailed characterization. The simple preparation procedure and reasonable cost of the spinel-type catalysts present a good potential for the thermal treatment of polychlorinated aromatic pollutants at lower temperatures.

Uptake by roots and translocation to shoots of polychlorinated dibenzo-p-dioxins and dibenzofurans in typical crop plants.

Root uptake and subsequent translocation of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in 12 agricultural crops were comparatively investigated. All crop plants were exposed hydroponically to a mixture of three kinds of dioxin congeners over 4d. The root concentration factor (RCF) of dioxin showed a logarithmic correlation with extractable lipid content in plant root. On the assumption that the dioxin escaping via gas phase from nutrient solution in the closed container can evenly diffuse in the air and equally absorb onto the shoot tissues of the dioxin-exposed plant and their nearby blank control plant, the amount of translocated dioxin was estimated by subtracting dioxin content in the shoot tissues of the blank control plant from that of the dioxin-exposed plant, and then the transpiration stream concentration factor (TSCF) of dioxin was calculated. The TSCF values of PCDD/Fs largely varied according to the plant species, and the TSCF values of 2,4,8-TrCDF were a little higher than those for 1,3,6,8-TeCDD expect for zucchini. For 1,3,6,8-TeCDD, zucchini had the highest TSCF value of 0.0089, followed by pumpkin (0.0064) towel gourd (0.0027), and cucumber (0.0010), verifying plants of the genus Cucurbita have the higher abilities of dioxin translocation. The TSCF values of 1,3,6,8-TeCDD for wheat and sorghum were 0.0013 and 0.0012, respectively. For maize, soybean, rice, Chinese cabbage, tomato and garland chrysanthemum, translocation was an insignificant mechanism of dioxin contamination in shoot tissues.

Dioxin-like compounds in sediments from the Daliao River Estuary of Bohai Sea: Distribution and their influencing factors

The concentrations, compositional profiles, and potential ecological risk of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in sediments of the Daliao River Estuary were investigated. Total concentrations of PCDD/Fs, PCBs, and PCNs were in the range of 11.3-133.2 ng/kg dry weight (dw), 1 971-37 632 ng/kg dw and 33.1-284.4ng/kg dw, respectively. The total TEQ values varied from 0.37 to 4.08ng/kg dw, with the dominant contributions by PCDD/Fs, then by PCBs and PCNs. The spatial distributions of PCDD/Fs, PCBs and PCNs in the river estuary were much related to hydrodynamic conditions. The risk of contamination to the deeper sea was increased in the flood seasons. Moreover, our data confirmed that both organic matter in sediments and molecular properties of dioxin-like compounds were the factors which strongly influenced the partition behavior of these dioxin-like compounds between sediments and water phase in the estuarine zone.