Determination of polychlorinated dibenzo-p-dioxins and dibenzo-furans in solid residues from wood combustion by HRGC/HRMS

PCDD/PCDF were determined in solid samples from wood combustion. The samples included grate ashes, bottom ashes, furnace ashes as well as fly and cyclone ashes. The solid waste samples were classified into bottom and fly ash from native wood and bottom and fly ash from waste wood. For each of the four classes concentration distribution patterns from individual congeners, the sums of PCDD/PCDF and the international toxicity equivalents (I-TEQ) values are given. The I-TEQ levels of fly ash from waste wood burning can be approximately up to two thousand times higher than the values from fly ashes of natural wood. The I-TEQ levels in bottom ashes from waste wood combustion systems are as low as the corresponding ashes from the combustion of native wood. Grate ash samples from waste wood combustion systems with low carbon burnout show high levels of PCDD/PCDF.     

High performance of catalytic sheet filters of V2O5-WO3/TiO2 for NOx reduction

Environmental Science and Pollution Research - Nitrogen oxide (NOx) emissions in fuel from the stationary as well as from mobile sources primarily from power stations, industrial heaters,...     

The use of Pb isotopes to differentiate between contemporary and ancient sources of pollution in Greece

Stable lead isotopes are used to illustrate the relation source–receptor and to differentiate between sources of pollution in Greece. Air filters collected in the Kozani–Ptolemais lignite mining area, West Macedonia, point to an impact from gasoline lead as well as lead from the combustion of lignite. This is supported by lead isotope data of wheat grown on reclaimed land. Lead isotope analyses of contemporary teeth from the Lavrio sulphide mining area, southeast of Greece, show the imprint of previous mining activities as well as traffic emissions. Moreover, the Lavrio teeth can be distinguished from one tooth from Athens; the Athens tooth show a stronger impact of gasoline lead. Lead data also imply that the Greek top soil is contaminated by air pollution from earlier sulphide mining and smelting since Hellenic and Roman times.     

湿地甲烷排放研究进展

本文综述了湿地甲烷排放的研究进展,包括湿地甲烷排放的研究方法、时空变化、排放机制、影响因素以及主要湿地类型排放通量,并指出了今后研究方向及应注意的问题。     

Some Recent Experience with Fabric Filters for Paniculate Collection

EPA's “Third Symposium on Fabric Filters for Particle Collection,” held in Tucson December 5 and 6, 1977, emphasized the results obtained from both laboratory and field experience. Data from selected new and/or continuing research programs as well as from new pilot and field applications are reviewed.     

Electron donor capacity of reducing dissolved organic matter from crop residue decomposition as probed by chronoamperometry

Reducing dissolved organic matters (RDOMs) from the anaerobic decomposition of crop residue can greatly affect the physicochemical and biological properties of soils. Electrochemical methods that can effectively protect them from oxidation and rapidly obtain results, such as differential pulse voltammetry (DPV), have been applied to qualitatively analyzing properties of RDOMs. However, the donated amount of electrons from RDOMs as a capacity factor may be more crucial for evaluating their important roles. For the first time, matured chronoamperometry (CA) was applied to quantitatively determining the electron donor capacities of RDOMs in crop residue management. The electron donor capacities of RDOMs from green manure were much higher than those from rice straw, which indicated that the former had greater effect on the redox status and reactions of soil. Chronoamperometry was proposed as a practical and effective method to quantitatively characterize RDOMs from residue decomposition.     

苏州污水处理厂污泥干化工艺方案的比选

污泥处理及其处置所面临的重要问题之一，就是如何对城市污水处理厂产生的污泥进行有效减容，尽量降低对外部能源的需求。文中在掌握国内外污泥干化主要工艺技术的基础上，针对某城市污水处理厂的污泥干化工程，拟对采用燃煤烟气干燥、污泥消化一干化一体化、太阳能热泵干燥等三种不同污泥干化工艺进行物料、能量工艺核算。并在此基础上，计算初期投资与15年的运行费用总和。通过对燃料价格、环保和安全等影响因素的研究，分析比较了五种供热系统，以太阳能热泵供热系统为最优，值得大力推广和应用。     

Morphological,compositional and ultrastructural changes in the Scrobicularia plana shell in response to environmental mercury – An indelible fingerprint of metal exposure?

The study aimed to assess morphological, structural and compositional alterations in Scrobicularia plana nacre environmentally exposed to mercury in order to seek out the possibility of the assessed alterations as a monitoring tool to handle complexity and interactions of metals in the environment involving a non-invasive methodology. Bivalves were collected from a mercury contaminated site (Laranjo basin – Ria de Aveiro, Portugal) and a reference site in the same aquatic system. The combination of scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS) technique depicted a sheet like morphology of bivalve nacre collected from the reference site. Moreover, EDS plot exhibited the presence of potassium, oxygen, calcium, and carbon elements. Shells collected from the contaminated area depicted lamellar patches like structures with particle like morphology composition. SEM images corresponding to the elemental analysis by EDS plot clearly denoted the presence of mercury. SEM images from the other locations of the contaminated shells depicted large surface area, a broken or ruptured symmetry of organic matrix as well as crack-like gaps. The influence of environmental mercury affecting the surface morphology of S. plana nacre showed dimple like morphology (as proved by transmission electron microscopy, TEM). The possible explanation may be the replacement of calcium elements with other elements or alloys from the nacre composite collected from contaminated region. Therefore, the nacre fingerprint may be useful as innovative knowledge and applicable tool aiming at risk reduction from noxious mercury present in the environment. Overall results suggested the use of shell as an indelible fingerprint of metal exposure.     

Identification and Quantitative Analysis of Particulate Air Contaminants by X-Ray Diffraction Spectrometry

Because of the synergistic effects which take place from the mixing of gases and particulates in ambient air, it is important that the determination of air contaminants be carried out on the sample in its native state without imposing any further chemical recombination during the analysis. Since x-ray diffraction provides a chemically passive method of analysis and yields molecular rather than elemental information, we have undertaken the siudy of, and have successfully employed crystal diffraction lines as a qualitative and quantitative means for determining such materials as lime, calcium carbonate, road salt, coke dust, and aerosol from sinter emissions as well as several other less common industrial particulates in samples obtained from dustfall as dispersed in a matrix of powdered amorphous glass. Correlative to the above investigation this method was also extended to the study of such gases as sulfur dioxide which may be selectively fixed to an active surface.     

Investigation of the solvent extracts of humic organic matter (HOM) isolated from the Ravenna Lagoon to study environmental pollution and microbial communities

Solvent extracts of HOM isolated from highly polluted sediments from the Ravenna Lagoon were studied. Diagnostic indicators included polycyclic aromatic hydrocarbons (PAHs) and nonylphenols as hazardous organic pollutants to characterize anthropogenic pollution, as well as fatty acids (FA, analysed as methyl esters, FAME) to characterize microbial communities responsible for natural attenuation processes. The distribution of PAHs including cyclopentafused surrogates pointed to a significant pyrogenic origin, characteristic for methane combustion. The PAH distribution was characterized by high concentrations of highly carcinogenic analytes with molecular weights of 276Da (benzo[ghi]perylene prevailing) and 300Da (coronene prevailing). The PAH pattern as obtained by solvent extraction was very different from that obtained from pyrolysis/thermochemolysis of the HOM polymeric matrix. The FA pattern indicated strong bacterial input, with a significant contribution from methanotrophic bacteria as revealed by monounsaturated members with n:1omega8 and n:1omega5 double bonds in the alkyl chain. Terrestrial inputs as revealed by FAME analysis beyond C(20) with pronounced even-over-odd discrimination were of minor significance. This was confirmed by the pattern of nC(24)-nC(30) alcohols in strong even-over-odd prevalence occurring in relatively low concentrations. The hopane hydrocarbon distribution reflected a distinctive impact from industrial processes utilizing heavy fractions of petroleum as feedstock. Hopanols along with the 17beta(H),21beta(H)-bishomohopanoic acid pointed to hopane producers, including methanotrophic and sulfate-reducing bacteria. Nonylphenols, which could not be detected in the pyrograms of solvent-extracted HOM matrix, had a total concentration of about 70microg g(-1) referred to the HOM in the solvent extract. In addition to common phytosterols including beta-sitosterol, coprostanol could be detected in the solvent extracts pointing to human fecal matter contamination. Concentration of resin acids turned out to be very low, thus no harmful environmental effects are to be expected from these compounds.     

Evaluation of mutagenic potential of contaminated atmosphere at Ibirapuera Park, São Paulo - SP, Brazil, using the Tradescantia stamen-hair assay

We report seasonal variation in CH(4) and N(2)O emission rate from solid storage of bovine manure in Delhi as well as emission factors and emission inventory from manure management systems in India. Emission flux observed in the year 2002-2003 was 4.29+/-1, 4.84+/-2.44 and 12.92+/-4.25 mg CH(4)kg(-1)dung day(-1), as well as 31.29+/-4.93, 72.11+/-16.22 and 6.39+/-1.76 microgN(2)O kg(-1)dung day(-1) in winter, summer and rainy seasons, respectively. CH(4) emission factors varied from 0.8 to 3.3 kg hd(-1)year(-1) for bovines and were lower than IPCC-1996 default values. N(2)O emission factors varied from 3 to 11.7 mg hd(-1)year(-1) from solid storage of manure. Inventory estimates were found to about 698+/-27 Gg CH(4) from all manure management systems and 2.3+/-0.46 tons of N(2)O from solid storage of manure for the year 2000.     

Methoxyphenols from burning of Scandinavian forest plant materials

Semivolatile compounds in smoke from gram-scale incomplete burning of plant materials were assessed by gas chromatography and mass spectrometry. Gas syringe sampling was shown to be adequate by comparison with adsorbent sampling. Methoxyphenols as well as 1,6-anhydroglucose were released in amounts as large as 10 mg kg(-1) of dry biomass at 90% combustion efficiency. Wood, twigs, bark and needles from the conifers Norway spruce and Scots pine emitted 12 reported 2-methoxyphenols in similar proportions. Grass, heather and birchwood released the same 2-methoxyphenols but also the corresponding 2,6-dimethoxyphenols which are characteristic of angiosperms. The methoxyphenols are formed from lignin and differ in structure by the group in para position relative to the phenolic OH group. Prominent phenols were those with trans-1-propenyl and ethenyl groups in that position. Vanillin, 4-hydroxy-3-methoxybenzaldehyde, was a prominent carbonyl compound from the conifer materials.     

Contribution of Burning of Agricultural Wastes to Photochemical Air Pollution

Agricultural wastes from orchards, grain fields, and range lands are burned each year in California as the most practical means of ridding the land of these wastes. In order to determine the relative contribution of the burning of such material to photochemical air pollution, the effluent from 1 23 fires of known weights of range brush, both dry and green, barley and rice stubble, and prunings from various fruit and nut trees were monitored in a special tower which provided an open burning situation. Analyses were made for total hydrocarbon, expressed as C, by flame ionization detection, and for 24 individual hydrocarbons by gas chromatography, as well as for CO and CO₂ by infrared spectroscopy. A few analyses were made for oxides of nitrogen. These data, coupled with temperature and airflow measurements, allowed calculations to be made on pounds of effluent per ton of material burned and demonstrated that the emissions from agricultural burning are much less than those from the automobile, a principal source of such emissions.     

不同深度处理工艺去除污水处理厂出水中氮磷的比较研究

城市污水厂出水直接进入天然水体、或经过深度处理后回用于灌溉、补充景观水体和回灌地下水,均需要进行安全性评价.针对北京市北小河污水处理厂出水经过深度处理后回用于奥运公园的安全性,比较了不同深度处理工艺对营养盐(氮、磷)总量和不同形态的去除效果.研究表明,二级处理本身对氮磷的去除效果十分有限,回用水需经过深度处理.在所研究的生物活性炭吸附、微滤、超滤、反渗透以及上述技术的组合工艺中,使用超滤和反渗透联用的工艺路线对脱氮除磷的效果较为理想,其他工艺对去除氮磷的效果十分有限.     

不同深度处理工艺去除污水处理厂出水中氮磷的比较研究

城市污水厂出水直接进入天然水体、或经过深度处理后回用于灌溉、补充景观水体和回灌地下水,均需要进行安全性评价.针对北京市北小河污水处理厂出水经过深度处理后回用于奥运公园的安全性,比较了不同深度处理工艺对营养盐（氮、磷）总量和不同形态的去除效果.研究表明,二级处理本身对氮磷的去除效果十分有限,回用水需经过深度处理.在所研究的生物活性炭吸附、微滤、超滤、反渗透以及上述技术的组合工艺中,使用超滤和反渗透联用的工艺路线对脱氮除磷的效果较为理想,其他工艺对去除氮磷的效果十分有限.     

Adsorption of phenolic compounds from aqueous solutions by a water-compatible hypercrosslinked polymeric adsorbent

A water-compatible hypercrosslinked polymeric adsorbent (NJ-8) for adsorbing and removing phenolic compounds from their aqueous solutions was prepared. This product can be used directly without a wetting process. Its adsorption property toward four phenolic compounds, phenol, p-cresol, p-chlorophenol, and p-nitrophenol was tested using the commercial Amberlite XAD-4 as a reference. The capacities of equilibrium adsorption for all four phenolic compounds on the NJ-8 from their aqueous solutions are around two times as high as that of Amberlite XAD4 within the temperature range 283-323 K, which may contribute to their micropore structure and the partial polarity on the network. Freundlich isotherm equations, as well as relative adsorption capacities and isosteric adsorption enthalpies for the four phenolic compounds, indicate that the adsorption of phenolic compounds on the NJ-8 resin is a physical adsorption process. Mini-column adsorption studies for phenol on Amberlite XAD4 and NJ-8 resins show that the breakthrough adsorption capacities are 0.54 and 0.99 mmol/ml, and the total capacities are 0.62 and 1.37 mmol/ml, while no extra acetone was needed to remove the adsorbed phenol from NJ-8 as from Amberlite XAD4.     

Polycyclic aromatic hydrocarbons in wastewater, WWTPs effluents and in the recipient waters of Beijing, China

In this study, surface water samples from the Wenyu River and the North Canal, effluent from major wastewater treatment plants (WWTPs) in Beijing, and wastewater from open sewers that discharge directly into the river system were collected and analyzed for 16 priority USEPA polycyclic aromatic hydrocarbons (PAHs). Concentrations of these 16 PAHs ranged from 193 to 1790 ng/L in river surface waters, 245 to 404 ng/L in WWTP effluents, and 431 to 2860 ng/L in the wastewater from the small sewers. The WWTP effluent was the main contributor of dissolved PAHs to the river, while wastewater from the small sewers contributed both dissolved and suspended particulate matter-associated PAH to the river as indicated by the high dissolved organic carbon and suspended particulate matter contents in the wastewater. Although the flow from each open sewer was small, a PAH discharge as high as 44 kg/year could occur into the river from these types of sewers. This amount was equivalent to about 22 % of the PAH loads discharged into the North Canal downstream from Beijing, whereas the remainder was mainly released by the major WWTPs in Beijing.     

Green Biomass Materials in Polyurethane Foams

Flexible polyurethane foams were prepared using naturally derived materials as alternatives to conventional auxiliary blowing agents. This research was based on the concept held by some that natural chemicals are better as a part of industrial ecology. The authors have attempted to define the foam manufacturing suitability of natural chemicals, but have not defined or defended the policy implications of such choices. Natural chemicals are often less suitable than those refined from petroleum and may then need some environmental credit related to greater discharge to be viable substitutes. Modest decreases in density (relative to foams without any auxiliary blowing agent) were obtained with the addition of solid CO₂ but other physical properties were not measured. It is unclear whether the reduction in density is a result of the phase change of CO, from solid to liquid within the polyurethane cell matrix or simply a bubbling effect of C02 in solution causing voids within the final product. Although it was anticipated that the high boiling point of limonene, from citrus peeis, would negate effectiveness as an auxiliary blowing agent, there were analogous decreases in foam density. The observed effect might be rationalized by the significant vapor pressure of limonene at temperatures lower than the boiling point. The limonene may be sweptf rom the foam system coincident with the loss of in situ generated CO₂ isoprene, naturally emitted from deciduous vegetation as well as from the combustion of carbonaceous fuels, provides a useful, if not complete, range of foam densities and may then be a partial substitute for halogenated auxiliary blowing agents. Switching from methyiene chloride to isoprene as the auxiliary blowing agent of choice would immediately decrease organic emissions from polyurethane foam plants by 20 percent (molecular weight effect). Regulation as a VOC and the residual acrid odor may be potential drawbacks to commercial utilization of isoprene.     

Characterization of the organic matter of sludge: determination of lipids, hydrocarbons and PAHs from road retention/infiltration ponds in France

This paper presents the results of the organic matter characterization of sludge from two ponds (retention and infiltration) located in France. Special focus was placed on studying hydrocarbons and PAHs. This investigation is part of a global project on road and urban sludge with the aim of identifying a better means for managing these materials. Gas chromatographic and GC/MS analyses indicate that the main component of the organic fraction stems from petroleum-derived products like diesel fuel and motor oil. This finding was confirmed by the presence of biomarkers from the hopane series, as well as by pyrolytic and alkylated PAHs. Results from this study clearly show that the contaminants are mainly generated from anthropogenic petroleum sources. Due to their levels of hydrocarbon contamination, these sludge deposits must be considered as waste and cannot therefore be disposed anywhere, especially within the current context of sustainable development.     

Occurrence of residues of the veterinary drug malachite green in eels caught downstream from municipal sewage treatment plants

Residues of malachite green (MG), a veterinary drug illegally used for the treatment of aquacultured fish, have been found in wild eels caught from surface waters downstream from the sewers of different municipal sewage treatment plants (STPs). MG and its metabolite leucomalachite green (LMG) were detected with total concentrations up to 0.765 microg kg(-1) fresh weight in the tissues of 25 out of 45 eels caught from different lakes, a river and a canal in Berlin, Germany. In all cases, the occurrence of the residues could directly be linked to the presence of discharges by municipal STPs into the receiving surface waters. MG is a multiple-use compound that is also used to color materials. Thus, it appears to be reasonable that the residues of MG found in the eel samples originate from such uses, e.g. by wash off from clothes or paper towels colored with MG. Additional loads from legal uses of MG as veterinary drug for the treatment of ornamental fish (private aquaria) are possible. The results obtained from this study are the first proof of background contaminations of a veterinary drug found in samples of fish not intentionally treated with such agents. MG and LMG are regarded as potential genotoxic carcinogens making it impossible to establish a tolerable daily intake. A margin of exposure (MOE) approach was applied to evaluate the human health risk associated with the consumption of the eels investigated in this study. With a MOE of 3.4 million the chronic risk was classified as being very low. Nevertheless, due to their potential to act as genotoxic carcinogens, any oral exposure to residues of MG and LMG should be avoided. According to European Union law, zero tolerance applies to all residues of MG and LMG found in food for human consumption as MG is not registered for use as veterinary drug.