稠环芳烃和多环芳烃成因模拟

通过模拟实验发现：硫与β－胡萝卜素反应可以形成稠环芳烃,硫或氧与联苯反应可以形成多种多环芳烃。稠环芳烃主要是以一个合适的分子为基础发展形成的,多环芳烃也可以由一个分子转化形成,但主要是两个或两个以上联苯等化合物分子连接起来而成。     

贵阳市环境中多环芳烃的研究

多环芳烃(PAHs)是两个或两个以上苯环连接在一起的烃类化合物;环境中它主要来源于煤、石油、木材、有机高分子化合物、烟草和其他碳氢化合物的不完全燃烧.PAHs在环境中无处不在,且具有致癌性、致畸性、致突变性,生物累积性使它能长期滞留在环境中.因此PAHs的研究受到了环境工作者的极大关注.准确把握环境中多环芳烃的行为、主要来源及归宿,对有效控制污染、保护人类健康有非常重要的意义.     

污染土壤中多环芳烃的微生物降解及其机理研究进展

多环芳烃(PAHs)是一类普遍存在于环境中的难降解危险性“三致”有机污染物。微生物对多环芳烃的降解是去除土壤中多环芳烃的主要途径。研究表明，对于土壤中低分子量多环芳烃类化合物，微生物一般以唯一碳源方式代谢；而大多数细菌和真菌对四环或四环以上的多环芳烃的降解作用一般以共代谢方式开始。本文重点论述了高分子量多环芳烃：芘和苯并(a)芘的微生物降解及其机理。并介绍了多环芳烃污染的微生物—植物联合修复机制，最后展望了污染土壤中多环芳烃的研究趋势。     

北京密云房山地区土壤中多环芳烃的组成与分布特征

选择北京城近郊房山与密云地区的土壤进行了多环芳烃的定量分析，同时探讨了多环芳烃在土壤中的分布特征与来源。研究结果显示：密云、房山两地土壤中多环芳烃的含量值具有明显差异，提示了两地工业活动影响强度的不同；各采样区土壤中多环芳烃总量的平均值在45．98～388．23ng／g变化，根据多环芳烃的特征参数可以推测研究区土壤中的多环芳烃主要来自于化石燃料的不完全燃烧。     

太原市区土壤中多环芳烃污染特征研究

采用1个样/km2的密度,1个分析组合样/25km2的方法,对太原市区土壤中多环芳烃进行了调查。结果表明,太原市区土壤中多环芳烃的平均含量为8.65μg/g;空间分布上北高南低,高值点主要位于工业区及交通要道地段;组成上以四环及四环以上的多环芳烃为主。通过与国内外城市土壤的对比可知,太原市土壤PAHs污染已相当严重,其来源主要是煤炭的燃烧。太原市工业布局、能耗类型和地理位置是造成土壤PAHs污染的主要原因。     

徐州土壤多环芳烃的环境地球化学迁移特征

选择江苏徐州黄棕壤进行不同深度层位多环芳烃含量的定量分析,研究并探讨了多环芳烃在土壤深度剖面中的地球化学迁移特征。研究结果显示,多环芳烃在徐州土壤剖面中主要集中在地表0~20 cm内。其中低环多环芳烃化合物的迁移能力较强,4~6环等高环化合物相对较难迁移,主要残留于地表生态系统环境中。     

贡嘎山海螺沟降雪中多环芳烃的短周期分布特征及来源分析

2013年1月在贡嘎山海螺沟3个不同采样点共收集了多个雪样,利用GC-MS分析了雪样中16种优控多环芳烃的含量,探讨了多环芳烃的短周期分布特征与来源,估算了采样点与排放源的直线距离。结果显示,海螺沟各采样点雪样中多环芳烃的总含量在163.7 ng/L~281.4 ng/L之间,其中菲的含量最高。雪样中2~4环多环芳烃占多环芳烃总量的百分比为92.0%~93.7%,表明污染来自较远距离传输,但主要排放源离海螺沟的直线距离不超过357 km。将雪层与气象资料的降雪期对应,结果表明从2012年11月到2013年1月这个短周期内,海螺沟雪样受多环芳烃污染的程度没有太大变化。对海螺沟雪样中的多环芳烃进行了来源分析,结果表明海螺沟雪样中的多环芳烃主要来自煤燃烧,不排除少部分木材燃烧,这一源解析结果与海螺沟及其周边地区主要以煤炭作为燃料的能源特征相吻合。     

拉萨市拉鲁湿地多环芳烃污染及其来源

通过分析采集的土壤、沉积物和大气样品,对拉萨郊区的拉鲁湿地多环芳烃污染及其来源进行了初步研究.湿地表层土壤中16种多环芳烃的平均含量的总含量为82.45×10^-9,既存在低环数的多环芳烃,又含有高环数的多环芳烃;湿地土壤中的多环芳烃主要来自于大气.     

第二松花江中下游河段底泥中多环芳烃的初步研究

第二松花江中下游河段8个底泥中多环芳烃（PAHs）分析表明，5种多环芳烃含量和多环芳烃总量随取样点位置发生明显的变化，城区河段底泥中各种PAHs含量和PAHs总量均高于非城区河段。2环加3环与5环PAHs化合物分布特点表明第二松花江中下游非城区河段底泥中PAHs的来源以石油类污染为主，而城区河段PAHs的来源则主要是化石燃料高温燃烧。第二松花江中下游河段（尤其是城区河段）底泥中PAHs具有较高生态风险，可能会对生物产生一定的负面影响。     

南黄海中部海水中多环芳烃的分布特征

2007年9月进行了2007南黄海海洋环境调查,并采集各个调查站位的表层、中层、底层海水及表层沉积物。利用液-液萃取法对采集到的样品进行前处理,并用气相色谱-质谱法检测海水中的多环芳烃。结果显示,监测站位中表层海水中总多环芳烃的含量范围是15.76~233.39ng/L,南黄海中部海水中多环芳烃的组成以2环的萘为优势组分;各种多环芳烃的含量与国际生物学组织或国家制定的评价水生生物暴露于水体的安全食用标准相比虽未超标,但个别组分如荧蒽的含量已达到生态毒理评价标准。     

Organic-Inorganic Interaction Recorded by Polycyclic Aromatic Steranes in Continental Epithermal Ore Deposits

Continental epithermal ore deposits are commonly associated with sedimentary organic matter, oils or solid bitumen. These organics embedded in mineral deposits can convey valuable information of the ore genesis. However, the extent to which the formation of ore minerals was recorded by organic compounds remains largely unknown, as also is how metal-rich ores interfere with the molecular proxies in the temperature regime envisaged for hydrothermal activity. The molecular compositional changes of ...     

芴系列化合物的成因

模拟实验揭示出:芴系列化合物的形成并不依赖于具有相同碳骨架的生物前身物质,在一定温度条件下,β胡萝卜素可以转化成芴系列,而硫和链状化合物反应可以形成更为丰富的芴系列化合物。β胡萝卜素在芳构化过程中会出现部分甲基脱落、甲基转移等变化,而且甲基上的活泼氢也会部分脱离,这样形成的自由基就可能结合成键形成芴系列;β胡萝卜素在热演化过程中生成的二苯甲烷系列可进一步转化成芴系列;硫在和链状化合物反应时也可能先形成一些二苯甲烷系列化合物,硫继续和这些产物反应会夺取两个苯环上的α位氢形成自由基,当一个苯环上的自由基和另一个苯环上的自由基结合时就可能形成芴系列。芴系列虽然具有生物骨架,但不能被认为是生物标志化合物,因为其地球化学合成作用形成的可能占多数。     

Levels of polycyclic aromatic hydrocarbons and polychlorinated biphenyls in sediment of bitumen deposit impacted area

Polycyclic aromatic hydrocarbons and polychlorinated biphenyls were investigated in sediment of bitumen deposit impacted area of Agbabu, Nigeria, to determine the present level of contamination with these toxic compounds prior to exploitation. Samples were collected during the dry season (March) and the wet season (August) of year 2008. Analysis was carried out with gas chromatography using mass spectrometry detector for polycyclic aromatic hydrocarbons and flame ionization detector for polychlorinated biphenyls. In the dry season sum of concentration of PAHs ranged from zero to 0.12 ± 0.06 ppm, while in the wet season the minimum was 0.18 ± 0.07 ppm and the maximum was 1.04 ± 0.16 ppm. Most of these values were higher than sum of polycyclic aromatic hydrocarbons concentrations of 1–10 μg/kg indicating that they were likely to come from anthropogenic sources. Average concentrations of PAHs such as naphthalene and benzo (a) pyrene obtained in sediment in the wet season in some of the stations were higher than recommended limits. The linear regression analysis between sum of concentrations and percentage organic carbon showed no significant correlation in sediment in the dry season (r² = 0.0025) and in the wet season (r² = 0.1345). The predominance of 4–6 ringed polycyclic aromatic hydrocarbons and the ratios between pairs of individual polycyclic aromatic hydrocarbons showed that they are likely to have come from pyrolytic sources. No polychlorinated biphenyl congener was detected in the samples.     

Molecular characterization of phenanthrene-degrading methanogenic communities in leachate-contaminated aquifer sediment

The existence of polycyclic aromatic hydrocarbons in the various environments has aroused great environmental concerns due to their potential hazards to human health. The presence of polycyclic aromatic hydrocarbons in aquifer is particularly sensitive where groundwater is used as a source of potable water. Anaerobic biodegradation of polycyclic aromatic hydrocarbons is an attractive option for remediation of contaminated aquifer sediment. Bacterial and archaeal community structures of phenanthrene-degrading aquifer sediment under methanogenic condition were investigated using clone library analysis in combination with microcosm study. The bacterial members were all affiliated with ??-Proteobacteria. Phylum Euryarchaeota was the predominant archaeal group, represented by genera Methanosarcina, Methanobacterium and Thermogymnomonas. Both bacteria (genera Citrobacter and Pseudomonas) and archaea (genus Methanosarcina) might have links to phenanthrene degradation process. This work might provide some new insights into developing strategies for the isolation of the putative polycyclic aromatic hydrocarbons degraders under methanogenic condition and bioremediating polycyclic aromatic hydrocarbons in leachate-contaminated aquifer sediment.     

Solvent–water extraction method for the evaluation of polycyclic aromatic hydrocarbons bioavailability in coal–tar-contaminated soils

A solvent–water extraction method was proposed as an assessment tool to estimate the bioavailability of polycyclic aromatic hydrocarbons in coal–tar-contaminated soils. The approach taken was to measure the percent of polycyclic aromatic hydrocarbons extracted by a solvent–water mixture and comparing the results with the percent of polycyclic aromatic hydrocarbons degraded in a soil slurry reactor. Five soil samples from three former manufactured gas plant sites and a coal–tar disposal site which were operated between 1880 and 1947, and 1945 and 1950, respectively, in Iowa, USA were used in this study. Extraction experiments were conducted using acetone–water or ethanol–water mixtures with solvent volume fractions ranging from 1.0 to 0.4 (v/v). The percent of polycyclic aromatic hydrocarbons extracted from the various soils decreased as the volume fraction of the solvent in the solvent–water mixture was reduced. An acetone–water mixture of 0.6 was found to be appropriate in correlating the percent of polycyclic aromatic hydrocarbons degraded to the percent of polycyclic aromatic hydrocarbons extracted. For the first correlation, the percent extracted and the percent biodegraded were modified by using the molecular weights and log K _ow of polycyclic aromatic hydrocarbons, respectively. For the second correlation, the equation relating the percent extracted and the percent biodegraded was modified using soil properties such as organic carbon content and percent of clay and silt. Although the experiments were conducted for a limited number of soils, the extraction method appeared to be a good starting point in estimating the bioavailability of polycyclic aromatic hydrocarbons in coal–tar-contaminated soils.     

噻吩系列化合物的形成机理模拟

通过模拟实验发现硫能和各种链状化合物反应形成噻吩系列化合物。其反应机理可能是：硫先作用于链状化合物将其改造成共轭烯中间体,其他硫再从这个部位进入碳骨架从而形成该类化合物。硫还可进一步和噻吩系列反应形成更复杂的含硫芳烃,而温度升高会促进这种反应,所以噻吩系列的含量可以作为成熟度指标,在沉积条件相同的前提下,噻吩系列含量高指示成熟度低,反之则指示成熟度高。     

Estimation of bioavailability of polycyclic aromatic hydrocarbons in river sediments

This study aimed to evaluate the total concentration of polycyclic aromatic hydrocarbons in sediments of Iguassu River in Southern Brazil. Alongside the concentration, the amount of such compounds bioavailable was also evaluated. This is accomplished by comparing its total amount present in sediments and the amount extracted by n-butanol. The results showed that the total concentration of polycyclic aromatic hydrocarbons presented in sediment ranged from 4.49 to 58.75???g/g. The total amount of polycyclic aromatic hydrocarbons extracted by n-butanol ranged from 1.22 to 17.07???g/g. The use of n-butanol represents the mimetic conditions that hydrocarbons, derived from oil, could be taken up by organisms. Most of the hydrocarbons extracted by n-butanol were those with lower octanol?Cwater partition constant, usually those with three and four rings. Compounds with more than four rings were extracted in lower or insignificant amounts. Even the hydrocarbons with lower molecular weight available may be degraded or eliminated by organisms, when accumulated. Estimating bioavailability of hydrocarbons represents what specific hydrocarbons could be available to be taken up by organisms.     

Biodegradation of polycyclic aromatic hydrocarbon by a halotolerant bacterial consortium isolated from marine environment

The biodegradability of polycyclic aromatic hydrocarbons such as naphthalene, fluorene, anthracene and phenanthrene by a halotolerant bacterial consortium isolated from marine environment was investigated. The polycyclic aromatic hydrocarbons degrading bacterial consortium was enriched from mixture saline water samples collected from Chennai (Port of Chennai, salt pan), India. The consortium potently degraded polycyclic aromatic hydrocarbons (> 95%) at 30g/L of sodium chloride concentration in 4 days. The consortium was able to degrade 39 to 45% of different polycyclic hydrocarbons at 60 g/L NaCl concentration. Due to increase in salinity, the percent degradation decreased. To enhance polycyclic aromatic hydrocarbons degradation, yeast extract was added as an additional substrate at 60g/L NaCl concentration. After the addition of yeast extract, the consortium degraded > 74 % of polycyclic aromatic hydrocarbons at 60 g/L NaCl concentration in 4 days. The consortium was also able to degrade PAHs at different concentrations (5, 10, 20, 50 and 100 ppm) with 30 g/L of NaCl concentration. The polycyclic aromatic hydrocarbons degrading halotolerant bacterial consortium consists of three bacterial strains, namely Ochrobactrum sp., Enterobacter cloacae and Stenotrophomonas maltophilia.     

Impact of coal tar pavement on polycyclic hydrocarbon distribution in lacustrine sediments from non-traditional sources

The evaluation of potential environmental impacts from polycyclic aromatic hydrocarbon is a subject that requires investigation, especially related to emission sources from highway roads with high traffic. In this paper, the distribution of polycyclic aromatic hydrocarbons was investigated in the surface sediments from a subtropical lake, located in the south of Brazil and away from urban areas. The results showed that all sediments presented such compounds in significant concentration, ranging from 9.50 to 29.88???g/g. The highest total concentration was found in those sites close to the highway (bridges) and the deepest area of the lake. Moreover, a high concentration of polycyclic aromatic hydrocarbons of high molecular weight, such as benzo(a)anthracene and dibenzo(a,h)anthracene was found. It was laso found that high concentrations might be related to asphalt and coal tar pavement used in the highway construction close to the lake. In addition, the potential capacity of sediment toxicity was compared with values of the interim sediment quality guidelines values. The results indicate that most of the sediment presents concentrations of hydrocarbons above these limits. Only fluoranthene and chrysene were found in concentrations below the guideline values. The concentrations of most of the polycyclic hydrocarbons are higher than the quality guidelines. However, the main concern is associated with the presence of benzo(a)anthracene whose concentration is 416 times higher than the limit establisehed by guidelines. The same observation can be done to traces of benzo(a)pyrene and dibenz(a,h)anthracene, with concentration values of 13 and 1,993 times higher.