降解多环芳烃的微生物的分离、鉴定方法及应用

阐述了降解多环芳烃的微生物的分离和鉴定方法;介绍了多环芳烃降解微生物的驯化方式;综述了多环芳烃降解菌的应用研究情况;对消除环境中多环芳烃污染问题的相关研究进行了展望并指出了将实验室筛选分离到的多环芳烃高效降解菌应用到实际环境中需解决的主要问题。     

火电厂排烟中颗粒物及多环芳烃的研究

对某火电厂电除尘器前后烟气中颗粒物的形貌、粒径分布及多环芳烃(PAHs)在颗粒物、烟气气相及原煤中的含量进行了研究.结果表明,颗粒物主要呈圆球形,主要成分为Al2O3和SiO2,除尘器前颗粒粒径主要分布在5～10 μm之间,其后以5 μm以下为主;电除尘器对大颗粒有较好的收尘效果,而对小于5 μm颗粒的收尘效果较差;低环PAHs在气相中的含量均高于颗粒物中的含量;电除尘器对PAHs的平均脱除率能达到89.74%,对4环和6环PAHs的脱除率高于90%.     

Sedimentary Record of Polycyclic Aromatic Hydrocarbons in the Gulf of Trieste (Northern Adriatic Sea)

To reconstruct a history of polycyclic aromatic hydrocarbon (PAH) pollution in the Gulf of Trieste, one of the largest urbanized areas in the Adriatic Sea, we analyzed three long sediment cores collected between 1996 and 1997. Concentrations of total PAHs, the sum of 16 PAH compounds and six of their methylated analogues, in all three cores show a decrease from 600–800 ng g⁻¹, at the surface, to levels below 250 ng g⁻¹ in deepest layers (down to 3 m). The same trend was shown with separate representative pyrogenic PAHs (pyrene, benzofluoranthene and phenanthrene). Using Hg as a recent geochronological tracer, we observe an increasing input of PAHs since the beginning of the 20th Century and, especially, after the Second World War coinciding with increasing industrialization and urbanization of the region. This correlation is supported by PAH ratios that are indication of combustion processes and represent a marker for anthropogenic inputs. No correlation exists between PAHs and black carbon within the core profiles, indicating two different fractions of the ‘black carbon continuum’.     

高活性萘降解细菌Hydrogenophaga Palleronii LHJ38的研究

为了研究微生物对多环芳烃的降解和转化规律,以萘作为研究对象,从餐厨油烟污染土壤中筛选到一株萘降解活性较高的细菌菌株,经菌种鉴定,定名为帕氏氢噬胞菌(H ydrogenophaga Palleronii)LH J38。测定了该菌的生长曲线和萘降解曲线,建立了菌株对萘的降解活性的定量测定方法,并研究了其最适生长条件。结果表明,在28℃、初始pH6.6、碳氮摩尔比为4的最适培养条件下,LH J38对初始质量浓度为2 000m g/L的萘在96h内的降解率可达98%以上;处于对数生长期的LH J38对萘的降解活性可达47.3nm o l/(m g.m in)。     

萘降解菌的筛选及其对多环芳烃的降解

从柴油污染土壤中筛选分离出一株萘降解菌N-3,进行了菌种鉴定及萘双加氧酶基因(nah)验证,并考察了该菌对不同种类多环芳烃(PAHs)的降解能力及降解过程中脱氢酶活性的变化。实验结果表明:该菌为铜绿假单胞菌(Pseudomonas aeruginosa),含有nah基因;当分别对液体培养基中质量浓度为50 mg/L的萘、菲、蒽、芘、芴降解84 h时,菌株N-3对萘、菲、蒽、芘、芴的降解率分别为28.81%,34.83%,36.65%,27.50%,23.47%。菌株N-3的脱氢酶活性与其对不同PAHs的降解率呈一定的正相关性。该菌不仅能有效降解萘,且对其他种类PAHs也有一定降解作用。     

Oil/Suspended Particulate Material Interactions and Sedimentation

The interactions of physically dispersed oil droplets with suspended particulate material (SPM) can be important for the transport of bulk quantities of spilled crude oil and polycyclic aromatic hydrocarbons (PAH) to subtidal sediments. The literature regarding oil/SPM interactions is reviewed, and results from whole-oil droplet/SPM interaction kinetics and pure-component (Prudhoe Bay crude oil distillate cut) equilibrium partitioning experiments are presented. The effects of oil type, SPM characteristics, and salinity on the interaction rates are examined, and the importance of whole-oil droplet/SPM interactions on particle agglomeration and settling behavior are discussed. Whole-oil droplet/SPM interactions are retarded as oil droplet dispersion into the water column is inhibited by oil viscosity increases due to evaporation weathering and water-in-oil emulsification. Compared to whole oil droplet/SPM interactions, dissolved-component/SPM adsorption is not as significant for transport of individual components to sediments. The information presented in this paper can be used to augment computer-based models designed to predict oil-spill trajectories, oil-weathering behavior, and spilled oil impacts to the marine environment.     

Spatial and Temporal Comparison of Polycyclic Aromatic Hydrocarbons and Spheroidal Carbonaceous Particles in Remote European Lakes

Spheroidal carbonaceous particles (SCP) and polycyclicaromatic hydrocarbons (PAH) have been measured in the dated sediment cores of 10 remote lakes distributed across Europe. The geographic trends were evaluated by examination of the superficial sediment fluxes and total sediment inventories. The highest levels of both markers were observed in the Eastern European lakes whereas the minimal values corresponded to the lake located in the Arctic. However, this SCP-PAH correlation was not observed after exclusion of the end member lakes from the series. The temporal trends of both pollutant markers are consistent with the history of pyrolytic emissions over Europe. However, the downcore SCP distributions are shorter than the PAH profiles in nearly all lakes. The differences are probably related to the different size particle fractions involved in the measurement of each marker, >5 and >1 m for SCP and PAH, respectively. Thus, the two proxies probably reflect pollution inputs from closer (SCP) and more distant sites (PAH).     

有机溶剂浸取石油污染土壤中的多环芳烃

采用索氏提取法和气相色谱分析了某炼油厂周边土壤中的多环芳烃的种类及含量,考察了6种有机溶剂对土壤中多环芳烃的浸取效果,探讨了溶剂与溶质溶解度参数差异对浸取效果的影响。结果表明:土壤试样中含有蒽、荧蒽、芘、、苯并[a]蒽、苯并[b]荧蒽、苯并[k]荧蒽和苯并[a]芘8种多环芳烃,其含量分别为4.20,22.05,10.62,4.26,5.54,0.80,0.94,4.18mg/kg;筛选出二氯甲烷作为土壤中多环芳烃的浸取溶剂;最佳浸取条件为浸取时间10min、浸取温度30℃、溶剂与土壤的液固比5∶1(mL/g)、土壤含水量8%,在此条件下,总多环芳烃浸出率为83.0%,各种多环芳烃的浸出率分别为蒽97.8%、荧蒽78.2%、芘99.9%、98.5%、苯并[a]蒽81.1%、苯并[b]荧蒽47.6%、苯并[k]荧蒽14.8%、苯并[a]芘58.7%。     

混合表面活性剂-浊点萃取法测定沉积物中多环芳烃的含量

以混合型表面活性剂（十二烷基硫酸钠（SDS）和对叔辛基苯基聚己二醇醚（Triton X-114））为萃取剂,采用浊点萃取法萃取沉积物中的15种多环芳烃（PAHs）,并利用HPLC技术测定15种PAHs的含量。实验结果表明,当混合型表面活性剂的加入量 3％（w）、混合型表面活性剂中SDS含量 50%（φ）、Na2SO4含量 8％（w）、萃取温度 60 ℃、超声萃取时间 10 min 时,15种PAHs的线性关系良好,r=0.998 9~0.999 7,检出限0.4~8.2 μg/L,加标回收率71.22%~97.36%,相对标准偏差0.92%~4.36%（n=6）。     

Biodegradation of Crude Oil Contaminating Marine Shorelines and Freshwater Wetlands

This paper is a summary of the various factors influencing weathering of oil after it has been released into the environment from a spill incident. Special emphasis has been placed on biodegradation processes. Results from two field studies conducted in 1994 and 1999 involving bioremediation of an experimental oil spill on a marine sandy shoreline in Delaware and a freshwater wetland on the St. Lawrence River in Quebec, Canada have been presented in the paper.     

石油污染海岸线生物修复技术研究进展

介绍了生物修复、生物强化和生物刺激的基本概念。综述了基于生物强化和生物刺激技术处理石油污染海岸线的研究进展,并指出不同处理技术的优势与不足。分析了影响溢油污染海岸线生物修复的重要因素,包括石油类型、波浪和水流能量、温度、盐度、氧气含量等。对今后研究的主要方向进行了展望。     

芳香族化合物的生物降解途径

分析了以苯、甲苯、萘和联苯为代表的芳香族化合物的生物降解途径,发现其共同点都是经过两步加氧酶作用生成二醇,最后再开环;介绍了苯、甲苯、萘和联苯这几种芳香族化合物分解酶的组分、相对分子质量及其辅基。     

多环芳烃污染土壤的微生物修复技术

对生物修复技术中的微生物进行了分类,并阐述了微生物生物降解土壤中多环芳烃（PAHs）的基本原理。在此基础上,分析了国内外微生物生物修复技术的发展概况,采用图示法重点综述了原位处理技术和非原位处理技术的工艺流程,并列举了相应的工程应用实例。     

表面活性剂在多环芳烃污染土壤修复中的应用

介绍了单一表面活性剂（非离子表面活性剂、生物表面活性剂）、阴-非离子混合表面活性剂对多环芳烃的增溶作用、增溶机理及无机离子对表面活性剂增溶能力的影响,综述了化学表面活性剂和生物表面活性剂在污染土壤生物修复中的应用。由于生物表面活性剂具有许多独特的优点,今后应加强生物表面活性剂的开发与应用研究。     

Characterisation of polycyclic aromatic hydrocarbons in flue gas and residues of a full scale fluidized bed combustor combusting non-hazardous industrial waste

This paper studies the fate of PAHs in full scale incinerators by analysing the concentration of the 16 EPA-PAHs in both the input waste and all the outputs of a full scale Fluidized Bed Combustor (FBC). Of the analysed waste inputs i.e. Waste Water Treatment (WWT) sludge, Refuse Derived Fuel (RDF) and Automotive Shredder Residue (ASR), RDF and ASR were the main PAH sources, with phenanthrene, fluoranthene and pyrene being the most important PAHs. In the flue gas sampled at the stack, naphthalene was the only predominant PAH, indicating that the PAHs in FBC’s combustion gas were newly formed and did not remain from the input waste. Of the other outputs, the boiler and fly ash contained no detectable levels of PAHs, whereas the flue gas cleaning residue contained only low concentrations of naphthalene, probably adsorbed from the flue gas. The PAH fingerprint of the bottom ash corresponded rather well to the PAH fingerprint of the RDF and ASR, indicating that the PAHs in this output, in contrast to the other outputs, were mainly remainders from the PAHs in the waste inputs. A PAH mass balance showed that the total PAH input/output ratio of the FBC ranged from about 100 to about 2600 depending on the waste input composition and the obtained combustion conditions. In all cases, the FBC was clearly a net PAH sink.     

活性炭固定床吸附分离溶液中表面活性剂和多环芳烃

利用活性炭固定床吸附分离表面活性剂和多环芳烃(PAH)的混合溶液,选取了具代表性的表面活性剂(TX100)和PAH(菲(PHE)等)。实验结果表明,流量越低、活性炭填充量越多、表面活性剂浓度越高、PAH浓度越低,越有利于表面活性剂的回收和PAH的去除。定义了有效回收时间,该时间是指PAH穿透10%的时间与表面活性剂穿透90%的时间之差,该时间越长,越有利于表面活性剂的回收。采用BDST和Thomas模型对TX100和PHE进行了吸附模拟,效果均较好;BDST模型拟合结果表明,当活性炭对TX100的吸附接近饱和时仍对PHE有较强的吸附能力。活性炭固定床吸附分离法可节约运行成本0.06元/L。     

Recent trends in the decomposition of chlorinated aromatic hydrocarbons by ultrasound irradiation and Fenton's reagent

Over the past few years, a large number of studies have been conducted on the use of ultrasound for decomposition of harmful organic pollutants, particularly chlorinated aromatic hydrocarbons (CAH) in wastewater. The published reports cover a variety of applications, including both ultrasonic treatment alone and in combination with other methods, e.g., advanced chemical oxidation processes. This article presents a review of recent work on ultrasonic-based methods of CAH decomposition, with emphasis on the applications of ultrasound alone and in combination with Fenton's reagent, as attractive advanced oxidation systems. In the first part of this review, the basic principles of sonochemical treatment are presented, followed by a review of the applications of ultrasound alone for CAH degradation. In the second part, the mechanisms of CAH degradation with Fenton's reagent and its application for CAH degradation are summarized. In the final part, studies on the applications of ultrasound together with Fenton's reagent are reviewed. The reported results suggest that a combination of ultrasound and Fenton's reagent is more attractive for practical application than the use of either method separately. Further studies, however, are required in this area because the reaction mechanism and the relationship between the reaction rates and process parameters for such a combined process are not yet well established.     

Evidence for biodegradation and volatilisation of dissolved petroleum hydrocarbons during in situ air sparging in large laboratory columns

Laboratory column experiments run for up to 13 days compared air sparging of groundwater contaminated by dissolved petroleum hydrocarbons in sterile and non-sterile aquifer sediments as well as uncontaminated sediments and groundwater. Loss of dissolved BTEX compounds in the contaminated columns was very rapid, occurring through volatilisation. The majority of the dissolved total organic carbon (TOC) persisted for much longer periods however. A direct comparison between losses from sterile and non-sterile columns suggested a negligible contribution of biodegradation to the removal of TOC. This was difficult to confirm through examination of O₂ utilisation because oxidation of a small amount of reduced sulphur in the aquifer materials was the dominant sink for O₂. Despite this, it was possible to conclude that less than 22% of the removal of TOC was through biodegradation during the first three days of air sparging.     

大气粉尘中常见多环芳烃类化合物的提取及含量测定

采用便携式PM2.5采样器和玻璃纤维滤膜对大气粉尘进行采样,以加压液体萃取、超声波辅助提取和微波辅助提取3种方法对多环芳烃类化合物进行提取,以超高效液相色谱和质谱联用方法进行测定。共检测出16种多环芳烃类化合物,分别为:萘、苊、苊烯、芴、菲、蒽、荧蒽、芘、苯并[a]蒽、■、苯并[b]荧蒽、苯并[k]荧蒽、苯并[a]芘、二苯并[a,h]蒽、茚并[1,2,3-c,d]芘和苯并[g,h,i]苝。3种提取方法均可有效提取大气粉尘中的多环芳烃类化合物,加压液体萃取法的提取效率最高、超声波辅助提取法次之、微波辅助提取法最低。超高效液相色谱和质谱连用方法可有效地分析大气粉尘中的多环芳烃类化合物,线性方程的相关系数不低于0.998 3,测定值的相对标准偏差不超过0.80%,检出限不高于0.27 ng/g。