本期推荐

正本期"水污染防治"栏目刊发了《低温等离子体技术改性填料前后Anammox工艺运行及微生物群落变化》(王淑雅,刘灵婕,王芬,季民)一文。近年来,厌氧氨氧化(anaerobic ammonium oxidation,Anammox)技术已日益成为废水生物脱氮领域的关键技术。Anammox生物膜工艺是常用的Anammox工艺类型,填料性能对Anammox     

光能自养生物膜形成机制及脱氮影响因素的研究进展

光能自养生物膜是一个由复杂微生物群落构成的相对稳定的微生态系统,微生物细胞及非生物物质镶嵌在微生物分泌的有机聚合物基质上,其显著特征是膜表面寄居着光能自养生长的微生物,并能在碳源缺乏条件下完成生物脱氮.总结了光能自养生物膜的形成机制,概述了光照、温度、微生物种类、营养物浓度对光能自养生物膜脱氮的影响,指出光能自养生物膜...     

电极改性对电极生物膜反硝化反应器硝酸盐氮去除性能的影响

探究在碳纤维毡电极上利用恒电压电化学聚合聚吡咯(PPy)的聚合效果,并利用傅里叶变换红外线(FTIR)及扫描电镜(SEM)对其进行表征;将聚吡咯覆膜改性后的碳纤维毡电极应用到自养反硝化的电极生物膜反应器(BER)中,考察电极改性对自养反硝化电极生物膜反应器的硝酸盐氮去除性能影响,并研究电极改性对生物膜附着量及生物膜微生物群落的影响。结果表明,恒电压电化学聚合能够在碳纤维电极表面形成均匀稳定的聚吡咯膜,从而实现聚吡咯在炭纤维毡电极上的覆膜改性。改性后的电极应用到自养反硝化电极生物膜反应器中,可使反应器对NO_3~--N的去除效率由对照反应器的67.3%增加到83.9%,处理效果提高了24.7%。对反应器内电极生物膜进行生物量测定和扫描电镜分析,可以看到R2反应器中改性电极生物膜附着量明显多于R1反应器中未改性电极生物膜的附着量,说明电极改性有利于生物膜的附着。电极生物膜微生物16S rDNA分析中R1反应器电极生物膜菌落组成中优势菌属为Dechloromonas sp.,而R2反应器电极生物膜的优势菌为Hydrogenophaga sp.(噬氢菌属)和Thauera sp.(陶厄氏菌属),两者有明显差别,并且R2反应器比R1反应器生物膜的菌落组成更多样化,这说明电极材料的改性对电极生物膜微生物群落的组成产生了影响。     

运行方式对低基质厌氧氨氧化系统脱氮及菌群结构的影响

为了考察运行方式对厌氧氨氧化系统脱氮性能及菌群结构的影响,建立一套厌氧移动床生物膜反应器,在(25±1)℃恒温、低基质(TN≤60 mg·L~(-1))条件下,分别以连续式和间歇式方式运行,采用高通量测序,基于直系同源蛋白簇基因(COGs),对16S rRNA扩增子测序结果进行功能预测,来表征微生物菌群结构和微生物功能的变化。结果表明:系统总氮负荷为(227±13) mg·(L·d)~(-1)时,间歇式运行脱氮效率(90.6%)优于连续式运行效率(74.6%),生物膜厌氧氨氧化细菌的相对丰度高于悬浮污泥;反应器由连续式变为间歇式运行后,主要功能菌属Ca. Brocadia丰度降低,同时,具有部分反硝化作用的Pseudomonas菌丰度出现明显升高。进一步分析可知,在适量的有机物条件下,间歇式运行能够获得更好的厌氧氨氧化与反硝化协同处理效果。本研究结果可为污水处理厂的实际运行提供参考。     

改性HDPE填料的制备及对MBBR脱氮除磷效果的强化

为解决传统填料亲水性差、挂膜速度慢等问题,对高密度聚乙烯(HDPE)填料进行亲水改性并改善填料的挂膜性能及在移动床生物膜反应器(MBBR)中的应用效果,用浸涂的方式将纳米SiO2、聚乙烯醇(PVA)、聚多巴胺(PDA)等材料涂覆在HDPE填料表面,对改性后填料进行接触角、 SEM、 FT-IR和XPS表征以及MBBR挂膜启动实验,研究化学需氧量(COD)、氨氮(NH3-N)、总氮(TN)、总磷(TP)的去除效果以及对填料挂膜时间、生物膜量、蛋白质和多糖含量的影响。结果表明：改性后,填料接触角由94.82°降至60.1°,填料亲水性明显增强;填料表面出现褶皱,粗糙度增加;上述材料成功负载在填料表面并引入了亲水基团且未改变填料基本结构;填料挂膜时间由25 d提前至16 d,挂膜时间提前了9 d, COD、 NH₃-N、 TN、 TP去除率分别达到94.9%、95.4%、83.5%、71.6%,与改性前比分别提高了9.3%、6.7%、13.7%、11.5%;填料的生物膜量是改性前的1.57倍,从27.35 mg·g^-1提高到42.87 mg·g     

KMnO4改性活性炭对臭气中甲硫醇的吸附特性

针对普通活性炭对污水厂臭气中甲硫醇吸附量低的问题,采用KMnO4浸渍改性以获得高甲硫醇吸附量的改性活性炭,通过低温氮吸附仪、扫描电子显微镜和Boehm滴定等表征揭示改性后活性炭吸附量提高的原因,并进行改性活性炭吸附甲硫醇的动力学和热力学研究。结果表明:在KMnO_4浓度为1%、温度为25℃、活性炭与浸渍液质量比为8∶100的条件下浸渍6 h,改性活性炭对甲硫醇的静态吸附量最高,达到344.22 mg·g~(-1),是未改性前的4.04倍:改性活性炭对甲硫醇吸附量提高的原因主要是表面碱性基团的增加(是原来的2.53倍),以及微孔容积和比表面积的增加。改性活性炭对甲硫醇的吸附符合准二级动力学模型,同时粒子内扩散模型显示吸附过程由气相扩散和内扩散共同作用;符合Freundlich吸附等温方程,具有多层吸附特征,且吸附容易进行,属于优惠吸附,是一个自发、放热和熵减的过程,升温不利于对甲硫醇的吸附。     

生物基质对SWIS脱氮效果及微生物的影响

为考察不同地下渗滤系统装置沿程脱氮效果的差异和脱氮微生物群落结构的分布状况,构建了2套改良装置(煤渣-生物基质的1~#、煤渣的2~#),对沿程出水的COD、氨氮、TN浓度和填料内的脱氮微生物丰度进行了测定分析。结果表明:系统在水力负荷为15 cm·d~(-1)下,1~#和2~#装置对氨氮平均去除率分别为75.59%、80.00%,对TN平均去除率分别为60.63%、57.96%,1~#的脱氮效果略优于2~#装置;由沿程氮污染物浓度变化可知,2套装置的TN去除范围主要在层高60～80 cm处。与2~#装置相比,添加生物基质的1~#装置TN去除率提高了9.60%,且其装置内的Bradyrhizobium、Pseudolabrys、 Dongia、 Rhodanobacter、 Rudaea等脱氮细菌的丰度也分别提升了0.51%、 1.52%、 1.02%、 10.49%和3.15%。因此,生物基质可促进SWIS内部脱氮微生物丰度提升,并通过提供反硝化的碳源来强化脱氮效果。     

铁屑耦合固相反硝化对低碳氮比废水中总氮的处理

为考察脱氮效率并解决碳源不足导致总氮(TN)去除率不高的问题,将竹刨花作为固体碳源与挂膜载体,引入铁屑,构成耦合体系,搭建2套反硝化实验装置(分别为耦合体系1号与单纯固相反硝化体系2号)并对脱氮率及微生物进行分析。结果表明：进水TN为41.62～59.95 mg·L^-1,COD/N<0.5,水力停留时间为18 h;13～105 d,1号TN平均去除率为73.21%～92.79%,比2号平均去除率高近1倍;1号碳源相对2号更为充足,但2体系出水COD均值都低于一级A;1号总铁释放稳定,出水总铁均值低于0.3 mg·L^-1,未出现NH3-N明显积累。SEM表征结果显示,1号竹填料表面黏性物质与微生物数量更多,生物膜更加紧密。16S rRNA表征结果显示：1号具有更高的微生物丰度与多样性;2体系反硝化脱氮相关门类占主体,优势门类均为变形菌门,但1号变形菌门占比高于2号;变形菌门中,1号反硝化菌群(属水平,丰度>1%)类别和总占比均高于2号。由此可知,铁屑强化了碳源的分解与利用,促进了脱氮功能菌生长,显著提升了耦合体系脱氮效能,出水TN可...     

组合人工湿地工艺微生物群落结构及脱氮效果研究

将复合垂直流、表面流、潜流3种不同类型的人工湿地串联起来,研究每种人工湿地的脱氮微生物及其脱氮效果.结果表明,各种人工湿地池填料表面微生物数量丰富,组合人工湿地系统形成两个串联的A/O单元,脱氮效果良好,其中总氮去除率达82.61%.     

种植不同植物的表面流人工湿地净化效果和微生物群落差异分析

为了解植物种类对表面流人工湿地的净化效果的影响及其与微生物群落的关系,研究了4种植物条件下表面流人工湿地的氮磷平衡以及微生物群落结构。结果表明,各组人工湿地对氨氮(45.53%～80.95%)、总氮(53.67%～80.30%)和总磷(32.97%～55.77%)都有较好的处理效果,种植植物的人工湿地比未种植的人工湿地具有更高的氨氮、总氮和总磷去除效果,其中黄菖蒲组对氮的去除效果最好,美人蕉组对磷的去除效果最好。在表面流人工湿地中,微生物作用(34.84%～45.44%)是人工湿地氮去除的主要途径,基质吸附(20.90%～23.91%)是人工湿地磷去除的主要途径,但是种植植物的人工湿地的氮磷通过微生物去除的量更高。高通量测序分析表明,相较于未种植植物的人工湿地,种植植物的人工湿地显示出更高的微生物丰富度、多样性和更高的脱氮除磷功能微生物的丰度。假单胞菌属、不动杆菌属、芽孢杆菌属和硝化螺菌属是人工湿地中主要的脱氮菌属,也是种植植物的人工湿地高生物脱氮的原因。假单胞菌属和不动杆菌属丰度增加是种植植物的人工湿地高生物除磷的原因。     

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.     

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.     

Meta-analysis of time-series studies of air pollution and mortality: effects of gases and particles and the influence of cause of death,age, and season

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 microg/m3 particulate matter (PM) of median diameter < or = 10 microm (PM10); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO2; 1.6% (1.1-2.0%) per 31.2 ppb O3; and 0.9% (0.7-1.2%) per 9.4 ppb SO2 (daily maximum concentration for O3, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM10 and SO2. Larger effect sizes were observed for respiratory mortality for all pollutants except O3. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Meta-Analysis of Time-Series Studies of Air Pollution and Mortality: Effects of Gases and Particles and the Influence of Cause of Death,Age, and Season

Abstract

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 μg/m³ particulate matter (PM) of median diameter <10 μm (PM₁₀); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO₂; 1.6% (1.1-2.0%) per 31.2 ppb O₃; and 0.9% (0.7-1.2%) per 9.4 ppb SO₂ (daily maximum concentration for O₃, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM₁₀ and SO₂. Larger effect sizes were observed for respiratory mortality for all pollutants except O₃. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验,研究表明：CPF-100的浓缩脱水效果优于PAM;当CPF-00投加量为1．16‰时,污泥沉降性能改善程度为37．51％;且在CPF-100投加量逐渐增大的初始阶段,污泥沉降性能改善程度随投加量的增加而增大,但CPF-100投加量也不宜过大,当CPF-100投加量超过1．16‰后,反而会使浓缩脱水效果变差。同时,建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型,其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

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。     

Experimental and statistical validation of SPME-GC-MS analysis of phenol and chlorophenols in raw and treated water

A procedure based on solid-phase microextraction (SPME) and gas chromatography coupled with mass spectrometry (GC-MS) was developed and validated in order to analyse 10 phenols in water samples. The optimised conditions were obtained using polyacrylate fibre (PA), 20ml of sample volume, 10% NaCl, pH 4.0 and direct extraction at 35 degrees C and 1000rpm, for 40min. The linear range and quantification limits for these compounds by SPME-GC-MS were defined. An evaluation of the main uncertainty sources of this method is included, which allows expanded uncertainties in the 9.4-35% range for the majority of the compounds. The main source of uncertainty is associated with matrix effects. The validated method is suitable for monitoring the production and distribution of potable water and was used, in field trials, for the analysis of samples from main intakes of water (surface or underground) and from water supply system of a large area (Lisbon and neighbour municipalities).     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

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.