2种曝气生物滤池的启动比较分析

分别采用陶粒和沸石作为曝气生物滤池的填料,在相同运行参数下进行曝气生物滤池启动对比研究,分析挂膜过程中COD、NH4+-N和浊度的去除效果。试验结果表明,在平均气温为30℃的条件下,2种曝气生物滤池都能很快完成启动挂膜,陶粒曝气生物滤池所需时间为12d,沸石曝气生物滤池所需时间为15d;陶粒曝气生物滤池具有更好的COD去除效果,沸石曝气生物滤池具有更好的NH4+-N去除效果;2个滤池对浊度都能够达到95%左右的去除率。     

沸石曝气生物滤池去除氨氮性能及生物学特征分析

天然沸石具有较大的孔隙率和比表面积,对氨氮有较强的选择性离子交换能力.运用天然沸石曝气生物滤池处理城市污水厂二级生化出水,结果表明,曝气生物滤池有良好的去除效果.在气水比为3∶1,水力负荷为1 m/h,温度＞20℃情况下,沸石曝气生物滤池对城市污水厂二级生化出水COD去除率为12.7%,NH3-N去除率为96.6%;试验系统沿程微生物活性和微生物量呈现逐渐下降趋势,而单位生物量的生物活性沿程分布则与此相反;曝气生物滤池对水中污染物的去除主要集中在底部进水端部分,当水流达到距进水端上方105 cm时,曝气生物滤池对水中NH3-N的去除率已达86.8%(占氨氮总去除率的90%),COD的去除率为13.3%(占COD总去除率的67%).     

城市污水处理厂出水低浓度污染物的生物降解研究

由于城市污水处理厂出水中含有的低浓度污染物的性能稳定而不易被去除,为探索一种快速、直接的低浓度污染物的深度处理方法,通过采用富二价阳离子斜发沸石作载体的生物沸石曝气滤池对某城市污水厂二级处理出水中的低浓度污染物的去除进行了实验研究,研究结果表明,当污水厂二级处理出水水质年平均指标NH3-N、COD、BOD5、TP及浊度分别为27.4 mg/L、57.2 mg/L、20.4 mg/L、1.7 mg/L和16 NTU时,采用两级生物沸石曝气滤池串联工艺,在第一级生物沸石曝气滤池装填3 m生物沸石,水力停留时间1 h,气水比为2∶1;第二级生物沸石曝气滤池装填2 m生物沸石,水力停留时间为0.5 h,气水比为1∶1,最终出水年平均指标NH3-N 0.13 mg/L、COD 7.55 mg/L(CODMn)、BOD50.78 mg/L、TP0.6 mg/L、浊度为0.13 NTU,出水水质可满足热力发电厂循环冷却补充水的水质要求.此种方法为污水处理厂的出水提供了经济有效的回用途径。     

生物沸石滤池处理富营养化水体的挂膜实验

采用上向流生物沸石滤池处理富营养化水体,考察了挂膜阶段(前30 d)滤池对浊度、COD和TP等的去除效果,重点研究了系统中各形态氮素(NH4+-N、NO2--N、NO3--N和TN)的变化情况。结果表明,对于富营养化水体,生物沸石滤池对浊度、COD和TP的去除率分别约为80%、30%和24%;出水NH4+-N始终保持在0.5 mg/L以下,去除率在90%以上;NO2--N出现峰值(4.98 mg/L,第9 d),第13 d后即一直低于进水值;实验后期出水NO3--N与进水NH4+-N变化趋势基本一致,表明硝化生物膜已成熟,原位再生可行;生物沸石床内可能存在同步硝化反硝化现象。出水NO2-N浓度低于进水可作为生物沸石挂膜成功的一个标志。     

臭氧曝气沸石生物滤池处理硝基苯废水

利用臭氧曝气沸石生物滤池处理硝基苯废水,了解了该方法对废水中的硝基苯、氮和磷的去除效果,考察了水力停留时间的变化对污染物去除效果的影响。臭氧曝气沸石生物滤池与空气曝气沸石生物滤池相比,臭氧曝气生物滤池对硝基苯、COD、氨氮的去除效果优于空气曝气沸石生物滤池,对总磷的去除效果与空气曝气沸石生物滤池差别不大。当臭氧曝气沸石生物滤池的HRT=4 h、臭氧浓度为126 mg/L时,对初始浓度为100 mg/L的硝基苯污水去除率接近99%。在相同条件下,空气曝气沸石生物滤池对硝基苯的去除率仅为59%。在HRT=4 h、臭氧浓度为126 mg/L时,臭氧曝气沸石生物滤池与空气曝气沸石生物滤池对COD的去除率为94%和83%,对NH+4-N的去除率为64%和59%,对TP的去除率为42%和45%。     

沸石曝气生物滤池去除氨氮性能及生物学特征分析

天然沸石具有较大的孔隙率和比表面积，对氨氮有较强的选择性离子交换能力。运用天然沸石曝气生物滤池处理城市污水厂二级生化出水，结果表明，曝气生物滤池有良好的去除效果。在气水比为3：1，水力负荷为1m／h，温度＞20℃情况下，沸石曝气生物滤池对城市污水厂二级生化出水COD去除率为12．7％，NH3-N去除率为96．6％；试验系统沿程微生物活性和微生物量呈现逐渐下降趋势，而单位生物量的生物活性沿程分布则与此相反；曝气生物滤池对水中污染物的去除主要集中在底部进水端部分，当水流达到距进水端上方105cm时，曝气生物滤池对水中NH3-N的去除率已达86．8％（占氨氮总去除率的90％），COD的去除率为13．3％（占COD总去除率的67％）。     

上向流好气滤池冬季挂膜启动及运行参数探讨

好气滤池同时具有普通滤池和曝气生物滤池的优点，能对二级出水中的COD、氨氮和浊度等指标进一步去除，提高再生水水质。试验探讨了冬季好气滤池的挂膜启动方法和运行参数，提出采用逐渐增加流量到设计流量的自然挂膜法，同时提出运行采用上向流；滤速1 m/h；气水比采用（1～3）∶1；填料填充高度与滤料直径有关；出水水头损失增加到1 m作为过滤周期的终点；适宜的冲洗强度冲洗滤池后，4 h内能恢复到滤池反冲洗前的处理状态。冬季低温条件延长了好气滤池的挂膜启动时间，但不影响挂膜质量；为保证出水质量，对好气滤池的运行滤速要通过试验确定。     

2种曝气生物滤池深度处理含CMC模拟退浆废水

采用陶粒滤料和活性炭滤料的2组曝气生物滤池(BAF)处理含CMC模拟退浆废水,在水力负荷0.071 m3·(m2·h)-1、水力停留时间24 h条件下,分析曝气生物滤池对COD、CMC和浊度去除效果和曝气强度对滤池运行的影响,研究滤柱高度方向污染物去除规律以及和微生物量、微生物活性间的关系。研究结果表明,随着气水比的增大,生物滤池对COD、CMC的去除效率增大,强烈的曝气作用会引起出水浊度增大。在气水比为4∶1的条件下,2组生物滤池对COD和CMC的平均去除率分别约为72%和65%、67%和62%。曝气生物滤池对COD、CMC、浊度的主要去除区域分别位于滤柱1.5、1.3和1.1 m高度以下区域。陶粒滤柱相对活性炭滤柱微生物量略高,两组滤池单位滤料微生物量和微生物脱氢酶活性沿滤柱高度方向变化趋势相似。两组滤池对CMC的去除主要依靠吸附作用,生物降解部分仅占CMC总去除率的34.7%和26.1%。     

硝化型曝气生物滤池的挂膜与启动

近年来,曝气生物滤池广泛应用于污水硝化过程中,硝化型曝气生物滤池应运而生。采用快速排泥挂膜法和自然挂膜法相结合的复合挂膜法,考察了进水是否含有机物对硝化型曝气生物滤池挂膜的影响。在19℃、HRT=55 min、出水DO=8 mg/L、进水NH4+-N约为50 mg/L的条件下,两滤池挂膜启动时间差异较大,进水不含有机物的1#滤池挂膜成功仅需18 d,当其运行稳定时NH4+-N的去除率达到100%;而进水含有机物的2#滤池挂膜成功需24 d,当其运行稳定时,COD和NH4+-N去除率分别为84.6%和91.2%。此结果表明,与含有机物的实际生活污水相比,采用不含有机物的模拟生活污水启动硝化型曝气生物滤池挂膜启动时间可缩短6 d,这主要是由于异氧菌产率系数比硝化菌大。     

叠式曝气生物滤池在给水预处理中的挂膜启动

针对低污染原水进行叠式曝气生物滤池的自然挂膜启动实验。在HRT为20～30 min,温度为28～33℃,气水比为0.5,滤速为12.5 m/h的条件下,研究分析叠式曝气生物滤池在自然挂膜启动过程中各项水质指标的变化情况与生物膜生长之间的相互关系,判断挂膜启动的进程。结果表明,在南方夏季,叠式曝气生物滤池能够进行快速启动,经过7 d左右自然挂膜启动完成,对CODMn的平均去除率为33%,对氨氮的平均去除率达到85.5%,对亚硝酸盐氮的去除率为82.9%。     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

Radionuclides in deer and elk from Los Alamos national laboratory and the doses to humans from the ingestion of muscle and bone

Abstract

This paper summarizes radionuclide concentrations (³H, ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu, ²⁴¹Am, and ^totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y^‐1 (2.2 μSv y^‐1), deer bone = 3.8 mrem y^‐1 (38 μSv y^‐1), elk muscle = 0.12 mrem y^‐1 (1.2 μSv y^‐1), and elk bone = 1.7 mrem y^‐1 (17 μSv y^‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y^‐1 (1000 μSv y^‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.     

Leaching of seven pesticides currently used in cotton crop in Mato Grosso State—Brazil

This study aimed to evaluate the leaching of pesticides and the applicability of the Attenuation Factor (AF) Model to predict their leaching. The leaching of carbofuran, carbendazim, diuron, metolachlor, α and β endosulfan and chlorpyrifos was studied in an Oxisol using a field experiment lysimeter located in Dom Aquino – Mato Grosso. The samples of percolated water were collected by rain event and analyzed. Chemical and physical soil attributes were determined before pesticide application to the plots. The results showed that carbofuran was the pesticide that presented a higher leaching rate in the studied soil, so was the one representing the highest contamination potential. From the total carbofuran applied in the soil surface, around 6 % leached below 50 cm. The other pesticides showed lower mobility in the studied soil. The calculated values to AF were 7.06E-12 (carbendazim), 5.08E-03 (carbofuran), 3.12E-17 (diuron), 6.66E-345 (α-endosulfan), 1.47E-162 (β-endosulfan), 1.50E-06 (metolachlor), 3.51E-155 (chlorpyrifos). AF Model was useful to classify the pesticides' potential for contamination; however, that model underestimated pesticide leaching.     

Endosulfan in China 2—emissions and residues

Background, aim, and scope  Endosulfan is one of the organochlorine pesticides (OCPs) and also a candidate to be included in a group of new persistent organic pollutants (UNEP 2007). The first national endosulfan usage inventories in China with 1/4° longitude by 1/6° latitude resolution has been reported in an accompanying paper. In the second part of the paper, we compiled the gridded historical emissions and soil residues of endosulfan in China from the usage inventories. Based on the residue/emission data, gridded concentrations of endosulfan in Chinese soil and air have been calculated. These inventories will provide valuable data for the further study of endosulfan. Methods  Emission and residue of endosulfan were calculated from endosulfan usage by using a simplified gridded pesticide emission and residue model—SGPERM, which is an integrated modeling system combining mathematical model, database management system, and geographic information system. By using the emission and residue inventories, annual air and soil concentrations of endosulfan in each cell were determined. Results and discussion  Historical gridded emission and residue inventories of α- and β-endosulfan in agricultural soil in China with 1/4° longitude by 1/6° latitude resolution have been created. Total emissions were around 10,800 t, with α-endosulfan at 7,400 t and β-endosulfan at 3,400 t from 1994 to 2004. The highest residues were 140 t for α-endosulfan and 390 t for β-endosulfan, and the lowest residues were 0.7 t for α-endosulfan and 170 t for β-endosulfan in 2004 in Chinese agricultural soil where endosulfan was applied. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell. We have estimated annual averaged air concentrations and the annual minimum and maximum soil concentrations across China. The real concentrations will be different from season to season. Although our model does not consider the transport of the insecticide in the atmosphere, which could be very important in some areas during some special time, the estimated concentrations of endosulfan in Chinese air and soil derived from the endosulfan emission and residue inventories are in general consistent with the published monitoring data. Conclusions  To our knowledge, this work is the first inventory of this kind for endosulfan published on a national scale. Concentrations of the chemical in Chinese air and agricultural surface soil were calculated for each grid cell. Results show that the estimated concentrations of endosulfan in Chinese air and soil agree reasonably well with the monitoring data in general. Recommendations and perspectives  The gridded endosulfan emission/residue inventories and also the air and soil concentration inventories created in this study will be updated upon availability of new information, including usage and monitoring data. The establishment of these inventories for the OCP is important for both scientific communities and policy makers.     

Impact of spiked concentrations of Cd,Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress)

This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment.     

Butyltin compounds in sediment and fish from the Polish Coast of the Baltic Sea

Concentrations of mono- (MBT), di- (DBT), and tri-(TBT) butyltin compounds were measured in eggs, liver, and muscle of nine species of fish from four regions of the Baltic Sea - the Firth of Vistula, the Gulf of Gdańsk, Puck Bay, and the mouth of the Vistula River. The overall concentration ranges among all the fish sampled from the four sites were: < 7 to 79 ng/g for MBT, 6 to 1100 ng/g for DBT, 7 to 3600 ng/g for TBT, and 16 to 4800 ng/g for total BTs, on a wet wt basis. The highest concentration of total BTs was found in herring liver from the Firth of Vistula (4800 ng/g, wet wt) and in roach muscle from Puck Bay (3300 ng/g, wet wt), while the least concentration was found in burbot eggs and liver from the Vistula River (39 and 32 ng/g, wet wt, respectively). TBT was the major form of BTs present in most samples analyzed. Sediment samples collected from shipyards in the Gulf of Gdańsk contained butyltin concentrations ranging from 1.2 to 46 μg/g (dry wt) for MBT, 2.0 to 42 μg/g for DBT, and 2.6 to 40 μg/g for TBT. As with the fish, the majority of the BTs in sediment were present as TBT, which suggested recent exposure of the aquatic environment of the region to TBT.     

Malathion-induced sublethal toxicity on the hematology of cricket frog (Fejervarya limnocharis)

The effect of malathion [diethyl(dimethoxythiophosphorylthio)succinate] at sublethal concentration (0.006 ppm) on hematological parameters of the cricket frog (Fejervarya limnocharis) was studied for 24 hrs to 240 hrs of exposure and remarkable hematological alterations were observed. The study on hematological parameters revealed a highly significant decrease (P < 0.01) in the total erythrocytes count in malathion-exposed animals from 24 hours to 96 hrs of exposure as compared to control. Significant decreases (P < 0.01) of hemoglobin and packed cell volume were also observed from 48 hrs to 240 hrs. A significant increase (P < 0.01) in leucocytes count was noted throughout the exposure period. Elevated numbers of lymphocytes and eosinophils as found in the present study revealed lymphocytosis as well as eosinophilia, suggesting that this was a result of direct stimulation of the immunological defense due to the presence of a toxic substance or may be associated with tissue damage. The cytomorphological and cytopathological study of erythrocytes and leucocytes in malathion-exposed frogs at 0.006 ppm concentration revealed various cytotoxic effects at different exposure times. It was noted that the size and the shape of the erythrocytes were subjected to variation in different blood disorders.     

Relation between forest vegetation, atmospheric deposition and site conditions at regional and European scales

Several monitoring programs have been set up to assess effects of atmospheric deposition on forest ecosystems. The aim of the present study was to evaluate effects on the understorey vegetation, based on the first round of a regional (the Netherlands) and a European forest monitoring program. A multivariate statistical analysis showed surprisingly similar results for both data sets; the vegetation appeared to be largely determined by the ‘traditional’ factors soil, climate, and tree species, but there was a small but statistically significant effect of atmospheric deposition. The effects of deposition include a slight shift towards nitrophytic species at high N deposition in the European network, and towards acidophytic species at high S-deposition in the Dutch network. The relatively small effect of atmospheric deposition is understandable in view of the very large natural variation in environmental conditions. Time series of both vegetation and environment are needed to assess deposition effects in detail.     

Influence of crop residues on trifluralin mineralization in a silty clay loam soil

Trifluralin is typically applied onto crop residues (trash, stubble) at the soil surface, or onto the bare soil surface after the incorporation of crop residues into the soil. The objective of this study was to quantify the effect of the type and amount of crop residues in soil on trifluralin mineralization in a Wellwood silty clay loam soil. Leaves and stubble of Potato (Solanum tuberosum) (P); Canola (Brassica napus) (C), Wheat (Triticum aestivum) (W), Oats (Avena sativa), (O), and Alfalfa (Medicago sativa) (A) were added to soil microcosms at rates of 2%, 4%, 8% and 16% of the total soil weight (25 g). The type and amount of crop residues in soil had little influence on the trifluralin first-order mineralization rate constant, which ranged from 3.57E-03 day^?1 in soil with 16% A to 2.89E-02 day^?1 in soil with 8% W. The cumulative trifluralin mineralization at 113 days ranged from 1.15% in soil with 16% P to 3.21% in soil with 4% C, again demonstrating that the observed differences across the treatments are not of agronomic or environmental importance.     

Concurrent nitrate and Fe(III) reduction during anaerobic biodegradation of phenols in a sandstone aquifer

The biodegradation of phenols (5, 60, 600 mg l⁻¹) under anaerobic conditions (nitrate enriched and unamended) was studied in laboratory microcosms with sandstone material and groundwater from within an anaerobic ammonium plume in an aquifer. The aqueous phase was sampled and analyzed for phenols and selected redox sensitive parameters on a regular basis. An experiment with sandstone material from specific depth intervals from a vertical profile across the ammonium plume was also conducted. The miniature microcosms used in this experiment were sacrificed for sampling for phenols and selected redox sensitive parameters at the end of the experiment. The sandstone material was characterized with respect to oxidation and reduction potential and Fe(II) and Fe(III) speciation prior to use for all microcosms and at the end of the experiments for selected microcosms.The redox conditions in the anaerobic microcosms were mixed nitrate and Fe(III) reducing. Nitrate and Fe(III) were apparently the dominant electron acceptors at high and low nitrate concentrations, respectively. When biomass growth is taken into account, nitrate and Fe(III) reduction constituted sufficient electron acceptor capacity for the mineralization of the phenols observed to be degraded even at an initial phenols concentration of 60 mg l⁻¹ (high) in an unamended microcosm, whereas nitrate reduction alone is unlikely to have provided sufficient electron acceptor capacity for the observed degradation of the phenols in the unamended microcosm.For microcosm systems, with solid aquifer materials, dissolution of organic substances from the solid material may occur. A quantitative determination of the speciation (mineral types and quantity) of electron acceptors associated with the solids, at levels relevant for degradation of specific organic compounds in aquifers, cannot always be obtained. Hence, complete mass balances of electron acceptor consumption for specific organic compounds degradation are difficult to confine. For aquifer materials with low initial Fe(II) content, Fe(II) determinations on solids and in aqueous phase samples may provide valuable information on Fe(III) reduction. However, in microcosms with natural sediments and where electron acceptors are associated with the sediments, complete mass-balances for substrates and electron acceptors are not likely to be obtained.