挥发性有机污染物与恶臭的生物处理技术及其工艺选择

本文介绍了生物滤池、生物洗涤塔和生物滴滤池处理挥发性有机污染物及恶臭的特性、近期发展状况及其应用。阐述了亨利系在选择生物处理技术中的应用,以及生物反应器内填料、微生物的选择。     

三相生物流化床处理生活废水

对三相生物流化床处理生活废水进行了实验研究，探讨了生物载体种类、溶解氧、水力停留时间及供气量对处理效果的影响。在选择的实验条件下，对进水CODcr值为600～1700mg／L的选定废水样，CODCr的平均去除率为85．8％。     

pH对生物滤池处理含H_2S和NH_3混合恶臭气体的影响

研究了pH对生物滤池处理含H2S和NH3混合恶臭气体的影响,以及不同pH下的物质转化情况和去除机制。结果表明,不同pH下,生物滤池对H2S和NH3的去除率是不同的。在强酸性(pH为2左右)和中性(pH为7左右)条件下,H2S均有较好的去除效果,这分别归于嗜酸性硫细菌和非嗜酸性硫细菌的生物降解作用。低pH下,NH3的去除归于化学中和作用;中性(pH为7左右)条件下,NH3有较高的去除率,主要依靠生物硝化作用。通过考察pH对生物滤池处理效果的影响,确定了生物滤池处理含H2S和NH3混合恶臭气体的pH控制条件和去除机制,为恶臭气体生物处理工艺的选择提供依据。     

控制挥发性有机污染物的革新方法—生物滴滤池法

欧洲及日本从７０年代开始研究用生物法降解挥发性有机气体。结果表明,生物法降解挥发性有机气体具有投资少,运行费用低,处理效果好,无二次污染等特点。在介绍生物法降解挥发性有机气体基本原理的基础上,主要讨论生物滴滤池填料的选择,菌种的驯化方法,运行条件的选择及运行工况的调节等,并指出存在问题和今后的技术发展方向。     

生物技术在有机废气处理中的研究进展

生物法净化有机废气主要有生物吸收法、生物滤池和生物滴滤池等几种形式。与传统的有机废气处理方法相比,生物技术具有费用低、处理效率高、安全性好及无二次污染等特点,在德国、荷兰、日本及北美等国得到广泛应用。     

微藻在生物减排CO2中的应用

微藻是一类单细胞或简单多细胞的微生物,其生长快速,并能够高效地固定各种来源的CO2,包括大气和工厂排放废气中所含的CO2及溶解性的碳酸盐.CO2的固定、生物能源的制备及污水的处理相结合为目前CO2的减排提供了一种前景非常好的技术选择.论述了热化学转化法(湿式碳化、热解及直接液化)等微藻生物质制备生物能源方法的研究状况,并分析了利用微藻生物减排CO2与污水处理相结合的可能性及目前的研究进展.     

生物法处理挥发性有机废气的研究

生物法处理被污染的空气这一技术已经被德国和荷兰成功地运用了 2 0年之久 ,但是在国内还属于一种较新的空气污染治理技术。本文主要概述了有机废气生物处理的 3种主要形式 :生物滤池、生物滴滤塔和生物洗涤器的原理、流程和几种影响反应器性能的因素 ,并比较了以上 3种反应器及其不同支撑材料的优缺点。目前 ,气态生物反应器主要以通用的指导方针、试验性的研究和来自类似应用的经验为基础进行设计的。     

生物法处理挥发性有机废气的研究

生物法处理被污染的空气这一技术已经被德国和荷兰成功地运用了20年之久，但是在国内还属于一种较新的空气污染治理技术。本文主要概述了有机废气生物处理的3种主要形式：生物滤池、生物滴滤塔和生物洗涤器的原理、流程和几种影响反应器性能的因素，并比较了以上3种反应器及其不同支撑材料的优缺点。目前，气态生物反应器主要以通用的指导方针、试验性的研究和来自类似应用的经验为基础进行设计的。     

污染物的原位生物处理—生物清消技术

生物清消技术是一种迅速发展的污染物处理的生物技术,用于处理分散在土壤、地下水、海洋和湖泊中的污染物。生物清消技术通过向环境供给营养物、共作基质和供氧,并依靠有机污染物自身的碳源促进天然微生物群体的生长繁殖,也可进一步向污染环境中补充在实验中筛选和增殖的微生物(强化技术)稳定和加速生物降解过程。本文介绍了生物清消的几种方法:生物促进法、生物耕作法、固相清消法、土壤堆制法、生物泥浆法,还介绍了强化技术应用的几个方面。     

电-生物耦合技术对偶氮染料的去除研究

酸性大红GR是一种较难生物降解的偶氮染料，采用一种电场和生物耦合的新型技术处理酸性大红GR模拟废水，并与单纯电化学法和好氧生物法进行试验对照。结果表明：反应6 h后，电化学法、好氧生物法、电-生物耦合技术对酸性大红GR的去除率分别达到15.7%、25.8%和71.2%，电-生物耦合技术能明显提高酸性大红GR的去除效果，起到强化生物处理的作用。在15 mA微电流条件下电-生物技术能克服50 mg/L酸性大红GR对好氧生物处理的抑制作用，为高浓度难降解染料废水的生物强化处理提供了可能。     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Effects of compositional heterogeneity and nanoporosity of raw and treated biomass-generated soot on adsorption and absorption of organic contaminants

A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N₂ surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

城市污水厂水质相关性及分布状态的研究和应用

采用统计学及质量控制的一些基本理论及方法对污水处理厂的运行数据进行分析,得出城市污水处理厂BOD5、COD、SS、TN、TP等主要出水指标呈正态分布的规律;城市污水BOD5、COD、TN、TP等指标间存在显著线性相关性的结论.研究结论可用于污水处理厂制定经济合理的出水监测方案以及对污水处理厂运行可靠性等进行评估.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

Quantification of carbamazepine and atrazine and screening of suspect organic contaminants in surface and drinking waters

A new approach for the identification of suspect trace organic contaminants in drinking and surface waters is presented. Samples were initially analyzed using a target determination method for two contamination tracers, carbamazepine (CBZ) and atrazine (ATZ). This method used offline solid-phase extraction and online solid-phase extraction techniques coupled to liquid chromatography-triple quadrupole mass spectrometry to accelerate the sample preparation process and improve method performance. CBZ and ATZ were found respectively in 31% and 56% of the samples, and concentrations were usually <20 ng L⁻¹. These samples were re-analyzed with a similar method on a quadrupole time-of-flight mass spectrometer to identify suspect contaminants by means of exact mass measurements and isotope patterns. A database of 264 common organic contaminants was built and used in conjunction with a Molecular Feature algorithm to identify the presence of these substances in drinking and surface water collected from different sources at various locations across Canada. Several organic contaminants were identified in the samples, but only the presence of caffeine, desethylatrazine, simazine and venlafaxine could be verified by comparison to pure standards. The presence of desethylatrazine was also confirmed by MS/MS experiments. These results suggest that target analysis for tracers of organic contamination may be a helpful tool to prioritize samples which should be further screened for suspect contaminants. This study also shows that the combination of separation techniques (offline and online SPE, LC) contribute to advance the applicability of high-resolution mass spectrometry for the identification of trace organic contaminants by accelerating the preparation step, reducing complexity and increasing analyte concentrations for optimal detection.     

Patterns and sources of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in surficial sediments of Lakes Erie and Ontario

This study determines spatial trends and congener patterns of 2378-substituted polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) in surficial sediments of Lakes Erie and Ontario. Sediments are enriched in 2378-PCDFs in Lake Ontario, and the PCDD/F concentrations increased from shallow near-shore sediments towards deep-water depositional zone sediments. In Lake Erie, sediments were dominated by octachlorodibenzo-p-dioxin, and the highest PCDD/F concentrations were observed in the western basin and the southern shoreline of the central basin with a decrease towards the eastern basin and the northern shoreline of the central basin. Principal components analysis revealed that chemical manufacture and disposal of chemical waste along the Niagara River has been a major PCDD/F source to Lake Ontario; while PCDD/Fs in Lake Erie are from multiple sources including industrial sources along the Detroit River, major tributaries along the southern shoreline of the lake, and atmospherically-derived material from the upper lakes and connecting channels.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.