Effects of copper and palladium on the reduction of bromate by Fe(0)

Bromate reduction by Fe(0) with incorporation of copper or palladium was investigated in batch tests. The incorporation of copper led to an increase in the rate of bromate reduction, while incorporation of palladium did not show any effect on bromate reduction by Fe(0), regardless of the bimetal application techniques (either simultaneous addition of Cu(II) or Pd(IV) into the Fe-BrO3- reaction system or using copper or palladium amended iron for bromate removal). Surface analyses by X-ray photoelectron spectroscopy (XPS) and X-ray powder diffraction (XRD) techniques indicated that aqueous Cu(II) was reduced and incorporated into the iron surface to form Cu2O and Cu(0). Among these two species, pure Cu(0) is not an active electron donor to the bromate reduction reaction, as shown by there being no reduction from using Cu(0) powders alone and no enhancement by Fe(0) when physically mixed with Cu(0). Although it has been proposed in the literature that the enhancement of adsorption also contributes to the enhancement of chemical reduction, this is not the case here because adsorption decreased when Cu increased. The enhanced bromate reduction rate in the presence of copper observed here is most likely the result of the newly formed active Cu(I). The presence of PdO was evidenced by XPS but yielded no enhancement in bromate reduction. Finally, the Cu2O present on the iron surface because of copper impurities in commercially available iron was found to be involved in the bromate reduction and to accelerate the reduction rate.     

Atmospheric concentrations and air-sea exchanges of nonylphenol, tertiary octylphenol and nonylphenol monoethoxylate in the North Sea

Concentrations of nonylphenol isomers (NP), tertiary octylphenol (t-OP) and nonylphenol monoethoxylate isomers (NP1EO) have been simultaneously determined in the sea water and atmosphere of the North Sea. A decreasing concentration profile appeared following the distance increasing from the coast to the central part of the North Sea. Air-sea exchanges of t-OP and NP were estimated using the two-film resistance model based upon relative air-water concentrations and experimentally derived Henry's law constant. The average of air-sea exchange fluxes was -12+/-6 ng m(-2)day(-1) for t-OP and -39+/-19 ng m(-2)day(-1) for NP, which indicates a net deposition is occurring. These results suggest that the air-sea vapour exchange is an important process that intervenes in the mass balance of alkylphenols in the North Sea.     

Macro analysis of spatiotemporal variations in ecosystems from 1996 to 2016 in Xishuangbanna in Southwest China

Environmental Science and Pollution Research - This study used remote sensing images from 1996 to 2016 as the main data source, and selected the average annual ecosystem type net change rate,...     

石油行业环境标准化现状分析

环境标准是环境管理的基础依据,中国石油行业在环境标准化方面做了大量工作,但是还存在许多问题。文章分析了石油企业环境保护标准化工作的进展和存在的问题,简述了国际、国内环境标准化工作面临的形势,提出了石油行业对环境标准化工作的需求。     

电除尘器的设计与探讨

介绍了电除尘器的工作原理、结构特性、基本参数和总体设计计算。这种电除尘器可广泛使用于冶金、化工、轻工 ,水泥和矿山等工业部门 ,随着人们对生态环境质量要求的不断提高 ,电除尘器将成为环保的重要设备     

Spatial spillover effects of urbanization on carbon emissions in the Yangtze River Delta urban agglomeration,China

Environmental Science and Pollution Research - To achieve a win–win situation for both urbanization and carbon emissions reduction from a spatiotemporal perspective, we need to identify the...     

Seasonal variations, temperature dependence, and sources of size-resolved PM components in Nanjing, east China

Size-segregated ambient particulate matter (PM) samples were collected seasonally in suburban Nanjing of east China from 2016 to 2017 and chemically speciated. In both fine (< 2.1 µm, PM_2.1) and coarse (> 2.1 µm, PM_>2.1) PM, organic carbon (OC) accounted for the highest fractions (26.9% ± 10.9% and 23.1% ± 9.35%) of all measured species, and NO₃⁻ lead in average concentrations of water-soluble inorganic ions (WSIIs). The size distributions of measured components were parameterized using geometric mean diameter (GMD). GMD values of NO₃⁻, Cl⁻, OC, and PM for the whole size range varied from < 2.1 µm in winter to > 2.1 μm in warm seasons, which was due to the fact that the size distributions of semi-volatile components (e.g., NH₄NO₃, NH₄Cl, and OC) had a dependency on the ambient temperature. Unlike OC, elemental carbon (EC), and elements, NH₄⁺, NO₃⁻, and SO₄²⁻ exhibited an increase trend in GMD values with relative humidity, indicating that the hygroscopic growth might also play a role in driving seasonal changes of PM size distributions. Positive matrix factorization was performed using compositional data of fine and coarse particles, respectively. The secondary formation of inorganic salts contributing to the majority (> 70%) of fine PM and 20.2% ± 19.9% of speciated coarse PM. The remaining coarse PM content was attributed to a variety of dust sources. Considering that coarse and fine PM had comparable mass concentrations, more attention should be paid to local dust emissions in future air quality plans.     

A review of neurotoxicity of microcystins

Cyanobacterial blooms-produced microcystins are secondary metabolites which can accumulate in the food chain and contaminate water, thus posing a potential threat to the health of aquatic animals and even humans. Microcystin toxicity affects not only the liver but also the other organs, i.e., the brain. The serious neurotoxicity effects caused by microcystins then lead to various symptoms. This review focuses on the neurotoxicity of microcystins. Microcystins can cross blood-brain barrier with the transport of Oatps/OATPs, causing neurostructural, functional, and behavioral changes. In this review, potential uptake mechanisms and neurotoxicity mechanisms are summarized, including neurotransmissions, neurochannels, signal transduction, oxidative stress, and cytoskeleton disruption. However, further researches are needed for detailed studies on signaling pathways and the downstream pathways of neurotoxicity of microcystins.     

Water quality of a tributary of the Pearl River, the Beijiang, Southern China: implications from multivariate statistical analyses

Water quality information of Beijiang River, a tributary of Pearl River in Guangdong, China, was analyzed to provide an overview of the hydrochemical functioning of a major agricultural/rural area and an industrial/urban area. Eighteen water quality parameters were surveyed at 13 sites from 2005 to 2006 on a monthly basis. A bivariate correlation analysis was carried out to evaluate the regional correlations of the water quality parameters, while the principal component analysis (PCA) technique was used to extract the most influential variables for regional variations of river water quality. Six principal components were extracted in PCA which explained more than 78% and 84% of the total variance for agricultural/rural and industrial/urban areas, respectively. Physicochemical factor, organic pollution, sewage pollution, geogenic factor, agricultural nonpoint source pollution, and accumulated pesticide usage were identified as potential pollution sources for agricultural/rural area, whereas industrial wastewaters pollution, mineral pollution, geogenic factor, urban sewage pollution, chemical industrial pollution, and water traffic pollution were the latent pollution sources for industrial/urban area. A multivariate linear regression of absolute principal component scores (MLR-APCS) technique was used to estimate contributions of all identified pollution sources to each water quality parameter. High coefficients of determination of the regression equations suggested that the MLR-APCS model was applicable for estimation of sources of most water quality parameters in the Beijiang River Basin.     

Coexisting sediments and suspended particles change the sorption of lindane and ciprofloxacin in waters

The real behavior of water organic contaminants such as pesticides and pharmaceuticals is not well known because research experiments usually simplify the conditions by studying the sorption of a pure compound on a single solid. However, in natural waters, biofilms, suspended particles, and sediments are solid substances that coexist, and thus may change the contaminant fate. Therefore, we studied here the sorption of lindane and ciprofloxacin by three single-solid and three double-solid sorbents using batch experiments. We also compared the effect of dissolved organic matter (DOM) between single- and double-solid sorption systems. Results show that the sorption quantity of lindane to the double-solid system of suspended particles and sediments is lower, of 0.99 L/g, than the sum of sorption quantity in the single-solid system, of 1.39 L/g. The sorption quantity of ciprofloxacin is higher, of 2.70 L/g, than the sum of sorption quantity in the single-solid system, of 1.90 L/g. These findings are explained by changes in DOM that suppress or promote sorption. To our best knowledge, this is the first study to present evidence that coexisting river solids modify lindane and ciprofloxacin sorption.