两种煤化工废水的产甲烷抑制性

通过间歇式产甲烷抑制实验,评价了两种煤化工废水#x02014;#x02014;焦化废水和鲁奇煤气化废水的产甲烷抑制性,并初步探讨了废水对产甲烷菌的抑制机理。实验结果表明：两种废水的产甲烷抑制性随废水加入量的增加逐渐增大;当废水加入量为400mL时,焦化废水的产甲烷抑制率达100%,鲁奇煤气化废水的产甲烷抑制率为50%;焦化废水对产甲烷菌的抑制性明显大于鲁奇煤气化废水。     

Possible alkylation of inorganic Hg(II) by photochemical processes in the environment

Contamination of surface waters by pesticides continues to be the focus of concern for water authorities due to the growing evidence of their deleterious effects on aquatic life. In this context, the present work investigates the occurrence of 16 selected pesticides belonging to the classes of triazines, phenylureas, organophosphates, chloroacetanilides and thiocarbamates in surface waters from the Llobregat River (NE Spain) and some of its tributaries (Anoia and Rubí) and assesses their potential impact on the aquatic organisms by applying a recently developed index, the Short-term Pesticide Risk Index for the Surface Water System (PRISW-1), which takes into account the pesticides concentrations and their overall toxicity against three aquatic organisms (algae, Daphnia, and fish). Chemical analysis, performed by means of a fully automated method based on isotope dilution on-line solid phase extraction-liquid chromatography-electrospray-tandem mass spectrometry (on-line SPE-LC-ESI-MS/MS), revealed diuron and diazinon as the most ubiquitous and abundant compounds with levels up to 818 and 132 ng L⁻¹, respectively. Total pesticide concentrations, which in only 1 out of 66 samples surpassed 500 ng L⁻¹, were higher in the tributaries than in the river but their contribution in terms of mass-loads to the overall pesticide pollution of the Llobregat River was relatively small. Contamination increased downstream of the river and was clearly influenced by rainfall and hence river flow. Application of the PRISW-1 index indicated that, although pesticides levels fulfilled the European Union Environmental Quality Standards (EQS) for surface waters, the existing pesticide contamination poses a low to high ecotoxicological risk for aquatic organisms, that algae and macro-invertebrates are at higher risk than fish, and that the organophosphates diazinon and malathion and the phenylurea diuron are the major contributors to the overall toxicity and therefore the most problematic compounds.     

Determination of organochlorine pesticide residue in sediment and water from the Densu river basin, Ghana

The distribution of organochlorine pesticides in the aquatic ecosystem from the Densu river revealed varying levels of concentration in water and the sediment samples. Three locations were sampled along the river to evaluate the levels of organochlorine pesticide residue in the river. Sediment and surface water samples were extracted by soxhlet and liquid-liquid extraction respectively and analyzed using Gas Chromatograph coupled with electron capture detector. The detectable organochlorine pesticides were gamma-hexachlorocyclohexane (HCH), delta-hexachlorocyclohexane, heptachlor, aldrin and dieldrin. The other pesticides that were investigated are gamma-chlordane, alpha endosulfan, endosulfan sulfate, p,p′-DDT and its metabolite p,p′-DDE, methoxychlor, endrin and its metabolite endrin aldehyde and endrin ketone. The order of increasing frequency of detection of samples was higher in sediment than water. In sediment, the mean concentration ranged from 0.030 μg kg⁻¹ dry weight (endrin) to 10.98 μg kg⁻¹ dry weight (aldrin). The highest detected concentration of organochlorine in water was endosulfan sulfate with mean concentration of 0.185 μg L⁻¹. Analysis of variance indicated significant differences for most organochlorine pesticide residue in the sediment sampled from the various locations. Some of the levels of organochlorine pesticides detected in water were relatively high compared to guideline values set by World Health Organization and Australia and thus could be harmful if the trend is not checked.     

China’s air pollution reduction efforts may result in an increase in surface ozone levels in highly polluted areas

China, as a fast growing fossil-fuel-based economy, experiences increasing levels of air pollution. To tackle air pollution, China has taken the first steps by setting emission–reduction targets for nitrogen oxides (NO_x) and sulphur dioxide (SO₂) in the 11th and 12th Five Year Plans. This paper uses two models—the Energy–Environment–Economy Model at the Global level (E3MG) and the global Chemistry Transport Model pTOMCAT—to test the effects of these policies. If the policy targets are met, then the maximum values of 32 % and 45 % reductions below ‘business as usual’ in the monthly mean NO_x and SO₂ concentrations, respectively, will be achieved in 2015. However, a decrease in NO_x concentrations in some highly polluted areas of East, North-East and South-East China can lead to up to a 10% increase in the monthly mean concentrations in surface ozone in 2015. Our study demonstrates an urgent need for the more detailed analysis of the impacts and designs of air pollution reduction guidelines for China.     

MTBE in California's Drinking Water: A Comparison of Groundwater Versus Surface Water Sources

During the last decade, the fuel oxygenate methyl tertiary butyl ether (MTBE) has received widespread attention as a potential threat to water quality, primarily due to leaking underground gasoline storage tanks and watercraft with two-stroke engines. In this article, we examine the annual detection frequency, number of new source detections, and concentration of MTBE detected in California's public drinking water groundwater and surface water sources from 1995 to 2002. This work builds on our previous evaluations of California's water quality monitoring database. However, it is unique in that it includes separate evaluations for groundwater and surface water sources that are of greatest concern to regulators, and which are likely being used for current public consumption. Our evaluations also include full-year data for 2002 (which have not been published previously) and an analysis of how the sampling and reported detections of MTBE vary by geographic location. We find that MTBE was generally detected (at any level) in approximately 0.5-0.9% and 0.2-0.4% of all groundwater sources assuming a one-detection and two-detection criterion, respectively. The overall detection frequency for MTBE in surface water sources is significantly higher than for groundwater sources, although these surface water detections appear to have substantially declined since 1996 (e.g., 7-9% for all surface water sources during 1996 to 1999 and 4% for all surface water sources during 2000 to 2002, assuming a one-detection criterion). The detection frequency of MTBE concentrations at or above the state drinking water standards in all drinking water sources (both groundwater and surface water sources) and the subset of drinking water sources that are likely to currently be delivered to consumers is markedly lower (and often zero). Despite the significant increase in water sampling over time, the number of new drinking water sources found to contain MTBE in California has not increased at the same rate and appears to have remained relatively stable or to have decreased since 1998. The data also show that nearly all of the 58 counties in California have routinely sampled at least some of their groundwater and surface water sources for MTBE over the last 8 years. Geographical evaluations show that MTBE has been detected (at least once) in groundwater sources in 34 counties and in surface water sources in 18 counties but has only been detected routinely (i.e., for 3 or more years) in 16 and 7 counties, respectively. Detected concentrations of MTBE are also generally below state drinking water standards, particularly for surface water sources. In short: (1) MTBE is rarely found in California groundwater or surface water sources that are of greatest concern to regulators or the public, and (2) drinking water detections of MTBE are expected to decline in the future due to the pending phase-out of MTBE and recent regulatory programs aimed at controlling gasoline releases from underground storage tanks and two-stroke-engine watercraft.     

Delineating landfill leachate discharge to an arsenic contaminated waterway

Discharge of contaminated ground water may serve as a primary and on-going source of contamination to surface water. A field investigation was conducted at a Superfund site in Massachusetts, USA to define the locus of contaminant flux and support source identification for arsenic contamination in a pond abutting a closed landfill. Subsurface hydrology and ground-water chemistry were evaluated in the aquifer between the landfill and the pond during the period 2005-2009 employing a network of wells to delineate the spatial and temporal variability in subsurface conditions. These observations were compared with concurrent measures of ground-water seepage and surface water chemistry within a shallow cove that had a historical visual record of hydrous ferric oxide precipitation along with elevated arsenic concentrations in shallow sediments. Barium, presumably derived from materials disposed in the landfill, served as an indicator of leachate-impacted ground water discharging into the cove. Evaluation of the spatial distributions of seepage flux and the concentrations of barium, calcium, and ammonium-nitrogen indicated that the identified plume primarily discharged into the central portion of the cove. Comparison of the spatial distribution of chemical signatures at depth within the water column demonstrated that direct discharge of leachate-impacted ground water was the source of highest arsenic concentrations observed within the cove. These observations demonstrate that restoration of the impacted surface water body will necessitate control of leachate-impacted ground water that continues to discharge into the cove.     

Photo-induced surface frustrated Lewis pairs for promoted photocatalytic decomposition of perfluorooctanoic acid

● Terminal carboxylate group activation is PFOA degradation’s rate-limiting step. ● Bi₃O(OH)(PO₄)₂ with surface frustrated Lewis pairs (SFLPs) efficiently degrade PFOA. ● Photo-induced Lewis acidic sites and proximal surface hydroxyls constitute SFLPs. ● SFLPs act as collection centers to effectively adsorb PFOA. ● SFLPs endow accessible pathways for photogenerated holes rapid transfer to PFOA. Heterogeneous photocatalysis has gained substantial research interest in treating per- and polyfluoroalkyl substances (PFAS)-contaminated water. However, sluggish degradation kinetics and low defluorination efficiency compromise their practical applications. Here, we report a superior photocatalyst, defected Bi₃O(OH)(PO₄)₂, which could effectively degrade typical PFAS, perfluorooctanoic acid (PFOA), with high defluorination efficiency. The UV light irradiation could in situ generate oxygen vacancies on Bi₃O(OH)(PO₄)₂ through oxidation of the lattice hydroxyls, which further promotes the formation of Lewis acidic coordinately unsaturated bismuth sites. Then, the Lewis acidic sites couple with the proximal surface hydroxyls to constitute the surface frustrated Lewis pairs (SFLPs). With the in-depth spectroscopic analysis, we revealed that the photo-induced SFLPs act as collection centers to effectively adsorb PFOA and endow accessible pathways to transfer photogenerated holes to PFOA rapidly. Consequently, activation of the terminal carboxyl, a rate-limiting step for PFOA decomposition, could be easily achieved over the defected Bi₃O(OH)(PO₄)₂ photocatalyst. These results suggest that SFLPs exhibit great potential in developing highly efficient photocatalysts to degrade persistent organic pollutants.     

天然淡水表面微层中某些重金属富集现象研究

自制成玻璃板表面微层水采样器,采集厚度可达30至55μｍ,表面微层水中颗粒物采集率为45.3％±2.2％,性能合乎要求。应用于天津水上公园表面微层湖水,以AAS和ICP法测定其中铜、铁、锰、锌的含量,与相应采样点下层湖水相比,4种重金属在表面微层水中的富集倍数为2至88,富集显著,并与采样站位等有关。     

Effect of atmospheric precipitation on the dissolved loads of the Dongjiang River, China

IntroductionTheatmosphericprecipitationhaslongbeenrecognizedasprovidinganinputofsubstancetothesurfacewaterandasourceofelementscarriedbyrivers (Stallard ,1981;Meybeck ,1983) .Itisestimatedthatapproximately 3 0 %ofsoluteloadsofworldriversarederivedfromthera…