3种载体固定化菌藻共生系统脱氮除磷效果的对比

采用3种不同载体（海藻酸钠、聚乙烯醇、复合载体）,分别将小球藻和栅藻与活性污泥固定成菌藻共生系统,制成菌藻凝胶小球,单独菌、单独藻的凝胶小球,用于处理人工污水。结果表明,（1）复合载体固定的菌藻共生系统氮磷去除效果最好,PVA载体的脱氮除磷效果次于复合载体优于海藻酸钠;（2）固定化菌藻共生系统的脱氮除磷效果明显优于单独固定菌和单独固定藻,固定菌的效果较差;（3）3种载体包埋下的固定化小球藻的脱氮除磷效果均较相同载体固定化的栅藻效果好。     

固定化藻菌去除海水冲厕污水中氮磷的实验研究

采用海藻酸钠凝胶包埋固定小球藻和活性污泥，对冲厕海水污水（模拟）中的氮磷污染物进行去除实验。结果表明，在藻菌比为2：1，固定化藻菌对氮磷的去除率分别达到95．5％和92．2％。在N／P为10时，固定化藻菌对冲厕海水污水中氮磷的去除效果最好。25～30℃时固定化藻菌对氨氮和磷的去除率最好，温度过高时藻和细菌细胞的活性受到抑制。固定化藻菌体系处理冲厕海水污水的较佳pH范围在6．5～8．5之间。     

固定化藻菌对珍珠蚌养殖废水中TN和TP去除效果的影响

将小球藻与有效微生物菌群(简称EM菌)、小球藻与活性污泥、小球藻与EM菌及活性污泥在同等条件下进行固定化处理,形成藻菌胶球(分别简称为CE、CA、CEA藻菌胶球),研究了3种藻菌胶球对珍珠蚌养殖废水中TN、TP的去除效果以及光照度、温度对3者脱氯除磷的影响,同时以无包埋藻菌胶球作为对照组进行96 h持续去TN、TP实验...     

藻菌混合固定化及其对污水的净化

首先将铜绿微囊藻和细菌在相同条件下共同培养,探索藻菌共生体系的最佳生长条件。然后将铜绿微囊藻和细菌混合固定化,比较混合固定和单独固定对污水中NH3-N和PO4^3--P的净化效率。结果表明,固定化混合藻菌体系对污水中NH3—N和PO4^3--P的去除效率明显高于单独固定化体系,并且随着实验时间的延长,对污水中NH3—N和PO4^3--P的去除效率逐渐升高。     

传统活性污泥工艺增强脱氮除磷功能的措施

传统活性污泥工艺以BOD、COD和SS为主要去除对象,对氮氮和磷的去除量很小.针对采用此类工艺的城市污水处理厂的现状,提出了增加脱氮除磷功能的一些措施,提供在城市污水处理厂改造工程中的参考.     

4种固定化藻类对污水中氮的净化能力研究

取培养至对数末期的藻，采用海藻酸钙凝胶包埋固定，对人工污水进行静态模拟净化试验，研究了蛋白核小球藻、鱼腥藻、双对栅藻和突变衣藻4种藻在固定和悬浮状态下，对污水中的氨氮和硝酸氮的净化效率以及藻类的生长特性。结果表明：固定化藻细胞比悬浮态藻细胞具有生长更趋于稳定、藻类的活性保持时间更长的优势。4种藻类中，小球藻和鱼腥藻在污水中的生长状况更好，较适宜采用海藻酸钙凝胶包埋固定化技术。实验第5 d时，固定化小球藻、鱼腥藻、双对栅藻和衣藻对NH₃-N去除率分别为91.9%、84.8%、68.3%和51.2%；对NO^-₃-N的去除率分别为85.1%、100%、96.9%和65.9%。固定化小球藻对NH₃-N的去除效果最好，而固定化鱼腥藻对NO^-₃-N的去除效果最好。因此，小球藻和鱼腥藻更适用于去除污水中的氮，具有很好的应用前景。     

人工湿地脱氮除磷特性研究

针对流域水体富营养化加剧和二级处理水氮磷指标较高的问题,提出以人工湿地对二级出水继续低耗、理想地脱氮除磷。研究中通过对照不同进水水质条件下,不同结构人工湿地的脱氮除磷效能,探讨了人工湿地内的主要脱氮除磷途径。研究表明,表面流湿地内植物对氨氮吸收／吸附和硝化过程为主要氮转化途径,潜流湿地内直接反硝化过程为主要脱氮途径,脱氮效率30％～40％;磷在人工湿地内主要依赖除磷填料床的物化吸附、共沉淀去除,除磷效率达80％以上。     

生物脱氮除磷工艺的研究进展

为遏制水体富营养化的恶化，氮，磷的排放标准日趋严格，生脱氮除磷工艺能有效地去除水体中的氮、磷。通过对现有的生物脱氮除磷传统工艺和新近发展工艺的介绍和分析，指出经济、高效、低能耗是其发展的方向，同时认为今后应加强对生物脱氮除磷机理更深入的研究，大力开发技术成熟，高效经济又符合我国国情的新工艺。     

凤眼莲-固定化氮循环细菌联合作用对富营养化水体原位修复的研究

应用生态工程技术和原理，在夏季利用凤眼莲（Eichhornia crassipes Mart.）结合固定化氮循环菌对富营养化水体进行原位修复研究。试验结果表明，凤眼莲+固定化氮循环细菌联合作用和单独的凤眼莲处理对富营养化水体总氮和铵态氮去除之间存在显著的差异，凤眼莲+固定化氮循环细菌联合作用对富营养化水体中总氮和铵态氮的去除率分别达77.2%和49.2%；而凤眼莲处理则分别达73.7%和32.3%；但两者对富营养化水体中硝态氮的去除没有显著差异。接种固定化氮循环微生物有利于水体中Chla、COD_Mn的降低和水体透明度的提高，但两者没有明显的差异。当凤眼莲处理系统接种固定化氮循环细菌时，除了氨化细菌变化不明显外，亚硝化菌，硝化菌，反硝化菌群数量比单独凤眼莲处理系统增加1～1.5个数量级，且接种固定化氮循环细菌还有利于凤眼莲生物量及其体内氮积累量的增加。     

固定化小球藻与活性污泥的共生系统处理含锌废水

研究固定化小球藻与活性污泥的共生系统对含锌废水中Zn2+的去除效果,分析菌藻状态、初始Zn2+浓度、pH、固定化菌藻小球投加量和菌藻体积比等5个因素对固定化菌藻共生系统去除Zn2+的影响。结果表明,固定化活性污泥、固定化小球藻和固定化菌藻对Zn2+的去除效果均优于悬浮小球藻,其中固定化菌藻对Zn2+的去除效果最好;废水中初始Zn2+浓度小于100 mg/L时,固定化菌藻系统对废水中Zn2+的去除率达到90.5%;固定化菌藻系统去除废水中Zn2+的最佳条件是:初始Zn2+浓度为80 mg/L,pH=7,固定化小球投加量为80 mL,菌藻体积比为1∶2。     

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.     

Dioxin- and POP-contaminated sites—contemporary and future relevance and challenges

BACKGROUND, AIM AND SCOPE: Once they have been generated, polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and other persistent organic pollutants (POPs) can persist in soils and sediments and in waste repositories for periods extending from decades to centuries. In 1994, the US EPA concluded that contaminated sites and other reservoirs are likely to become the major source of contemporary pollution problems with these substances. With this in mind, this article is the first in a new series in ESPR under the title 'Case Studies on Dioxin and POP Contaminated Sites--Contemporary and Future Relevance and Challenges', which will address this important issue. The series will document various experiences from sites contaminated with PCDD/F and other POPs. This article provides an overview of the content of the articles comprising the series. In addition, it provides a review of the subject in its own right and identifies the key issues arising from dioxin/POP-contaminated sites. Additionally, it highlights the important conclusions that can be drawn from these examples. The key aim of this article and of the series as a whole is to provide a comprehensive overview of the types of PCDD/F contaminated sites that exist as a result of historical activities. It details the various processes whereby these sites became contaminated and attempts to evaluate their contemporary relevance as sources of PCDD/Fs and other POPs. It also details the various strategies used to assess these historical legacies of contamination and the concepts developed, or which are under development, to effect their remediation. MAIN FEATURES: Special sessions on 'Contaminated sites--Cases, remediation, risk and policy' were held at the DIOXIN conferences in 2006 and 2007, and this theme will be continued at DIOXIN 2008 to be held in Birmingham. Selected cases from the approximately 70 contributions made to these sessions, together with some additional invited case studies are outlined together with the key issues they raise. By evaluating these cases and adding details of experiences published in the current literature, an overview will be given of the different features and challenges of dioxin and POP-contaminated sites. RESULTS: This article provides a systematic categorisation of types of PCDD/F and POP-contaminated sites. These are categorised according to the chemical or manufacturing process, which generated the PCDD/Fs or POPs and also includes the use and disposal aspects of the product life cycle in question. The highest historical PCDD/F and dioxin-like polychlorinated biphenyl (PCB) contamination burdens have arisen as a result of the production of chlorine and of chlorinated organic chemicals. In particular, the production of chlorinated pesticides, PCBs and the related contaminated waste streams are identified being responsible for historical releases of toxic equivalents (TEQs) at a scale of many tonnes. Along with such releases, major PCDD/F contaminated sites have been created through the application or improper disposal of contaminated pesticides, PCBs and other organochlorine chemicals, as well through the recycling of wastes and their attempted destruction. In some extreme examples, PCDD/F contaminated sites have also resulted from thermal processes such as waste incinerators, secondary metal industries or from the recycling or deposition of specific waste (e.g. electronic waste or car shredder wastes), which often contain chlorinated or brominated organic chemicals. The examples of PCDD/F and dioxin-like PCB contamination of fish in European rivers or the impact of contaminated sites upon fishing grounds and upon other food resources demonstrate the relevance of these historical problems to current and future human generations. Many of the recent food contamination problems that have emerged in Europe and elsewhere demonstrate how PCDD/F and dioxin like PCBs from historical sources can directly contaminate human and animal feedstuffs and indeed highlight their considerable contemporary relevance in this respect. Accordingly, some key experiences and lessons learnt regarding the production, use, disposal and remediation of POPs from the contaminated sites are summarised. DISCUSSION: An important criterion for evaluating the significance and risks of PCDD/Fs and other POPs at contaminated sites is their present or future potential for mobility. This, in turn, determines to a large degree their propensity for off-site transport and environmental accessibility. The detailed evaluation of contaminated site cases reveals different site-specific factors, which influence the varied pathways through which poor water-soluble POPs can be mobilised. Co-contaminants with greater water solubility are also typically present at such sites. Hence, pumping of groundwater (pump and treat) is often required in addition to attempting to physically secure a site. At an increasing number of contaminated sites, securing measures are failing after relatively short time spans compared to the time horizon, which applies to persistent organic pollutant contamination. Due to the immense costs and challenges associated with remediation of contaminated sites 'monitored natural attenuation' is increasingly gaining purchase as a conceptual remediation approach. However, these concepts may well prove limited in their practical application to contaminated sites containing persistent organic pollutants and other key pollutants like heavy metals. CONCLUSIONS: It is inevitable, therefore, that dioxin/POP-contaminated sites will remain of contemporary and future relevance. They will continue to represent an environmental issue for future generations to address. The securing and/or remediation of dioxin/POP-contaminated sites is very costly, generally in the order of tens or hundreds of millions of dollars. Secured landfills and secured production sites need to be considered as constructions not made for 'eternity' but built for a finite time scale. Accordingly, they will need to be controlled, supervised and potentially repaired/renewed. Furthermore, the leachates and groundwater impacted by these sites will require ongoing monitoring and potential further remediation. These activities result in high maintenance costs, which are accrued for decades or centuries and should, therefore, be compared to the fully sustainable option of complete remediation. The contaminated site case studies highlight that, while extensive policies and established funds for remediation exist in most of the industrialised western countries, even these relatively well-regulated and wealthy countries face significant challenges in the implementation of a remediation strategy. This highlights the fact that ultimately only the prevention of contaminated sites represents a sustainable solution for the future and that the Polluter Pays Principle needs to be applied in a comprehensive way to current problems and those which may emerge in the future. RECOMMENDATIONS AND PERSPECTIVES: With the continuing shift of industrial activities in developing and transition economies, which often have poor regulation (and weak self-regulation of industries), additional global challenges regarding POPs and other contaminated sites may be expected. In this respect, a comprehensive application of the "polluter pays principle" in these countries will also be a key to facilitate the clean-up of contaminated areas and the prevention of future contaminated sites. The threats and challenges of contaminated sites and the high costs of securing/remediating the problems highlight the need for a comprehensive approach based upon integrated pollution prevention and control. If applied to all polluting (and potentially polluting) industrial sectors around the globe, such an approach will prove to be both the cheapest and most sustainable way to underpin the development of industries in developing and transition economies.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

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.     

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.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Synthesis and characterization of m- and p-methylbenzyl-mercapturic acids derived from m- and p-xylenes

Chemical synthesis and physical properties of two mercapturic acids suggested as urinary metabolites of m- and p-xylenes ace described. These compounds may be used for the identification and quantivative determination by high-performance liquid chromatography of the corresponding mercapturic acids in urine.