太原市大气总悬浮颗粒物中正构烷烃和多环芳烃空间分布及来源分析

收集了太原市不同功能区的大气总悬浮颗粒物样品,经超声波提取分离得到正构烷烃、多环芳烃,经色谱-质谱分析表明,太原市大气颗粒物中正构烷烃主要来源于化石燃料的燃烧,少量为自然排放源。含量较高的不带取代基的多环芳烃有8种,其年平均浓度为1.50μg/m3,其中苯并(a)芘的年平均浓度为74.7ng/m3。多环芳烃的浓度分布为一电厂化工区>太钢工业区>桃园三巷商业居民区>太行仪表厂文化区。利用三角图与烟尘、汽车尾气样品中的多环芳烃特征相比较,认为太原市大气颗粒物中的多环芳烃主要来源于煤的燃烧。     

持久性有机污染物对环境的影响及对策

概述了《斯德哥尔摩公约》中规定的12种持久性有机污染物及六六六、多环芳烃等持久性有机污染物,以及持久性有机污染物对土壤、水体、农产品及大气的污染状况,并在借鉴国内外先进经验的基础上,根据中国的国情提出了5项对策.     

大气颗粒物源解释研究综述

大气物源研究是多学科共同探讨的较为复杂的问题.它对污染物的追踪、污染物的最终解释和评价具有重要意义,并为大气质量控制和环境管理提供合理依据.大气物源研究主要集中在颗粒物矿物学特征、化学成分及同位素组成等几个方面,并用数理统计方法建立起两者的相关关系,据此判别和解释大气污染物的来源.本文从矿物组成和形貌特征、标志性化学成分及同位素示踪等3个方面对近10余年来的研究成果进行较为系统的阐述.     

贵阳市大气环境中颗粒态多环芳烃特征

多环芳烃(PAHs)类物质具有致癌性、致畸性、致突变性和生物累积性,能长期留存在环境中[1].燃煤是多环芳烃的主要来源,贵阳市特殊的能源结构、地形和气候条件,造成了典型的煤烟型大气污染,我们首次研究了贵阳市大气颗粒物中颗粒态PAHs的特征.     

鼎湖山自然保护区大气气溶胶中的PAHs

多环芳烃（PAHs)是环境中分布广泛、危害人类健康的有机化合物，通过对鼎湖山自然保护区自然地理和大气气溶胶中苯并（a)芘分析认为，春季样品中大气气溶胶中PAHs主要来源于高等植物排放，夏季来源于珠江三角洲经济区化石燃烧排放。     

大气降尘TEM观察及其环境矿物学意义

在X射线衍射等分析研究基础上，进一步用透射电镜对半封闭室内长期沉积的大气降尘进行观察，提供了合肥地区大气降尘物相组成和各种物相形貌特征信息，揭示合肥地区大气污染物来源占第1位的是地表扬尘，以粘土矿物为标志；占第2位的是来源于大气化学次生气溶胶，主要和SO2、CO2、NOx等气态污染物排放有关，以石膏、碳酸盐和易溶盐类为标志；占第3位的是来源于汽车尾气排放的烟尘，以炭球为标志；占第4位的是来源于燃煤烟尘排放，以球形玻璃珠为特征。TEM调查不仅为合肥地区大气气溶胶颗粒成因、城市大气污染物来源和污染控制对策提供准确资料和依据，而且为确定大气颗粒物来源提供了有效研究方法和物源判别标志。     

燃烧麦秸对大气颗粒物中多环芳烃含量的影响

通过对集中燃烧麦秸前后北京市大气颗粒物中多环芳烃的分析，结合麦秸燃烧排放气体中相关成分的测试，说明燃烧麦秸对大气中多环芳烃的含量有很大的影响，提示有关部门应对之采取措施，防止大气环境质量因此而受到破坏。     

南岭山地湖泊多环芳烃的大气沉降历史记录

高大山脉对大气环流具有阻挡或屏障作用.通过分析测定南岭山地湖泊沉积物中多环芳烃(PAHs)的垂直分布,结合210Pb定年,探讨了大气PAHs污染在南岭山地的沉积历史.结果显示,沉积物中的PAHs主要以低环数化合物为主,其中尤以菲的含量为最高.在剖面深度0～28 cm范围内,总多环芳烃的含量范围为86～778 ng/g.自1970年开始,PAHs含量持续增加,其中20世纪80、90年代中后期PAHs含量略有降低;在2000年后,沉积柱中的PAHs含量呈急剧增加之势态.多环芳烃在大气迁移过程中发生了组成分异,沉积物中相对富集轻组分(低环数)PAHs,与颗粒物结合的大气干湿沉降是PAHs向偏远山地积的主要途径.     

兰州市大气总悬浮颗粒物中有机污染物分布特征及来源

对兰州市区、郊区大气颗粒物、汽车尾气及烟尘样品中的饱和烃和芳香烃进行了色谱－质谱检测，较为系统地对兰州市大气有机污染物来源做了定量、半定量研究。结果表明，兰州市大气有机污染物主要来源于人为因素，小部分为自然因素。人为污染源是复杂（包括工业生产、汽车尾气和燃煤等的排放）且严重的，应引起足够重视。     

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.     

环境中的多环芳烃及其生物恢复技术

多环芳烃是一大类广泛存在于环境中的有机污染物。天然燃烧、火山爆发、矿物资料及其它有机物的不完全燃料和热解产生的PAH进入大气中，气态沉降、城市地表径流、城市污水、废水及油的溢涵和渗漏等是PAH进行地表水的主要途径，大气中PAH的干、湿沉降，污水灌溉，地面及地下储油装置的渗漏，地面固体废物堆的淋滤等是土壤中PAH的主要来源，沉积物和土壤是PAH的主要环境归宿。生物恢复是一种处理有机污染的新方法。     

河北省宣化地区原煤与燃煤污染及其生态环境效应评价

通过对河北省宣化原煤及燃煤污染区表土和近地降尘的野外调查和样品分析,查明了表土及降尘中Hg、Cd、V、Zn、Mo、U、Mn、Cr等13种重金属元素及16种多环芳烃(PAHs)的地球化学特征。结果表明,原煤区土壤以Hg、Cd污染为主,污染区在煤带两侧约100 m范围内,燃煤区土壤以Hg、Cd、V污染为主,污染范围在燃煤企业下风口超过2 km。原煤区表土中Hg、Cd、Zn、Mo、U及PAHs与燃煤区表土中Hg、V、Mo、U、Mn、Cr及PAHs主要通过大气沉降带入。区内土壤中脲酶、碱性磷酸酶及β-葡萄糖苷酶活性均受到不同程度抑制,其中以β-葡萄糖苷酶最为明显,且燃煤区较原煤区抑制更为显著,反映了煤污染对土壤碳循环过程影响较大。     

多环芳烃在水稻籽粒中的分布及其与环境介质含量的关系

介绍了江西南昌某郊区采集的成熟期(2008年9月)和收割期(2008年10月)的水稻籽粒中多环芳烃(PAHs)的富集情况,并与同时期的环境介质(土壤、空气气相以及颗粒物)中多环芳烃的含量及分布情况作了相关性分析。结果表明,研究区水稻籽粒中16种多环芳烃(∑PAHs)总量平均为(74.8±13.6)ng/g,水稻土壤中∑PAHs含量平均为(203.7±14.3)ng/g,空气气相样品中∑PAHs含量平均为68.25 ng/m3,以3环和4环多环芳烃为优势化合物;颗粒物样品中∑PAHs含量平均为42.28 ng/m3,以4环、5环和6环多环芳烃为优势化合物。各介质多环芳烃含量在国内同类地区中均位于中等偏下水平。将多环芳烃在水稻籽粒和各个介质之间的生物富集系数与化合物的辛醇分配系数KOC、KOA作对数变换后比较,发现水稻籽粒中多环芳烃的分布与水稻土和空气颗粒物中的多环芳烃没有太大关系;而与空气气相中的多环芳烃关系较明显,证实了前人得到的气相化合物对植物体内化合物的分配起着主要贡献的研究结论。     

Levels and sources of polycyclic aromatic hydrocarbons (PAHs) in selected irrigated urban agricultural soils in Accra, Ghana

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments including urban soils. Elevated concentrations of PAHs in urban soils are caused by incomplete combustion of petroleum and coal. This study assesses 16 individual PAH compounds in a total of 112 surficial soil samples. The objective was to assess and compare the levels of contamination as well as examine the main sources of PAHs in four urban agricultural soils using molecular ratios of some specific hydrocarbons. The study showed that PAH levels in soil ranged from 1.23 ng/kg in soil collected from Dzorwulu to 2.95 ng/kg in soil collected from Ghana Broadcasting Cooperation (GBC) vegetable irrigation site. Of the total PAHs, the more water soluble PAHs (2–4 rings), which tend to be concentrated in the vapour phase were found to dominate the soils. The percentage dominance were Dzorwulu (52.8 %), Marine Drive (62.5 %), CSIR (53.2 %) and GBC (49.2 %). However, there were significant levels of the more carcinogenic PAHs (5–6 rings) present with percentages as 47.1, 37.5 46.8 and 50.8 % for Dzorwulu, Marine Drive, CSIR and GBC vegetable irrigation sites, respectively, and therefore, may impact negatively on public health. Based on the classification by the Institute of Soil Science and Plant Cultivation in Pulawy, Poland, urban soils in Accra could be classified as contaminated to different levels. Molecular ratios of Flu/pyr and PA/Ant were calculated to determine the main sources of PAHs. Results showed that PAHs could originate mainly from incomplete combustion of petroleum products, especially from atmospheric fallout from automobile exhausts. The study further showed that B(a)P concentration of 0.05 ng/kg in soil from GBC urban vegetable irrigation site requires immediate clean-up exercise and monitoring to mitigate human health impact.     

Concentrations and possible sources of PAHs in sediments from Bohai Bay and adjacent shelf

Concentrations, spatial distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency as priority pollutants were investigated in surface sediments of Bohai Bay, North China. Total concentrations of PAHs were in the range of 140.6–300.7 ng/g (dry wt), with an average of 188.0 ng/g. The three predominant PAHs were phenanthrene, acenaphthene and naphthalene. Sedimentary PAH concentrations of the north and central Bohai Bay were higher than those of the southern side of this bay. PAHs source analysis suggested that PAHs in most of the sediments were mainly from grass, wood and coal incomplete combustion. At other stations near the estuaries (Luanhe River Estuary and Chaohe River Estuary) or the oil drilling platform, both petrogenic and pyrogenic inputs were significant. The pyrogenic PAHs close to the oil drilling platform were mainly from petroleum combustion.     

北京市西北城区大气可吸入颗粒物中饱和烃的分布特征

利用气相色谱、气相色谱-质谱分析法从北京市西北城区四个季节大气可吸入颗粒物（PM10）中检测出种类丰富的饱和烃,主要包括正构烷烃、萜烷及甾烷等系列化合物。利用饱和烃的多项参数（如主峰碳数、碳优势指数CPI、藿烷22S/(22S+22R)比值等）对大气PM10中可溶有机物的来源及分布作了探讨。北京市西北城区PM10中正构烷烃的主峰碳数均介于23和27之间,而CPI值介于1和3之间,表明北京市西北城区PM10中的饱和烃均不同程度地受到了高等植物等现代生物和化石燃料（石油、煤等）不完全燃烧产物两种来源的影响,其中在春、夏季以高等植物、花粉、微生物等生物来源占比重较大,而在秋、冬季,尤其在冬季,化石燃料的不完全燃烧造成的污染比较明显。萜烷类物质的检出,表明北京市西北城区四个季节PM10中部分饱和烃来自于石油等化石燃料的不完全燃烧。甾烷类物质的检出,表明北京市西北城区四个季节PM10中部分饱和烃是来自于车辆释放的机油等。     

Black carbon in soils from different land use areas of Shanghai,China: Level,sources and relationship with polycyclic aromatic hydrocarbons

Black carbon (BC) in soils plays a key role of carrying hydrophobic pollutants like polycyclic aromatic hydrocarbons (PAHs). However, little is known about the spatial distribution, sources of BC and its relationship with PAHs in urban soils. We studied BC, total organic carbon (TOC) and PAHs concurrently in 77 soils collected from downtown area, suburban and rural area and industrial area of Shanghai, China. BC was determined by both chemical oxidation (dichromate oxidation, BC_Cr) and chemo-thermal oxidation (CTO-375, BC_CTO). BC sources were identified qualitatively by BC/TOC concentration ratios and BC-cogenerated high molecular weight (HMW) PAH isomer ratios and quantitatively by principal component analysis followed by multiple linear regression (PCA-MLR). Results showed that BC_Cr concentration (4.65 g/kg on average) was significantly higher than BC_CTO (1.91 g/kg on average) in Shanghai soils. BC_Cr concentrations in industrial area were significantly higher than those in other two. Stronger correlation was found between PAHs and TOC, BC_Cr than that between PAHs and BC_CTO, which indicates the possibility of PAHs being carried by charcoal and other organic matters thus negating its exclusive dependence on soot. Charcoal was therefore suggested to be taken into account in studies of BC and its sorption of PAHs. BC/TOC ratios showed a mixed source of biomass burning and fossil fuel combustion. PCA scores of BC-cogenerated HMW PAHs isomer ratios in potential sources and soil samples clearly demonstrated that sources of BC in urban soils may fall into two categories: coal and biomass combustion, and traffic (oil combustion and tire wear). PCA-MLR of HMW PAHs concentrations in soil samples indicated that coal and oil combustion had the largest contribution to BC in urban soils while tire wear and biomass combustion were important in downtown and rural area, respectively, which indicated they were main sources of HMW PAHs and presumably of BC.     

Source apportionment of elevated PAH concentrations in sediments near deep marine outfalls in Esquimalt and Victoria,BC, Canada: Is coal from an 1891 shipwreck the source?

Previous studies have suggested that coal from the 1891 shipwreck of a collier off Victoria, BC, Canada is responsible for elevated parent (unsubstituted) PAH concentrations in sediments near deep marine outfalls from Esquimalt and Victoria in the Strait of Juan de Fuca. To resolve this question, we analysed a comprehensive suite of resolved and unresolved complex mixture (UCM) alkanes, tricyclic terpane, hopane and sterane biomarkers, and parent and alkyl polycyclic aromatic hydrocarbons (PAHs) in samples of coal, wastewater and sediments. Composition patterns, principal components analysis (PCA) models and PAH and biomarker ratios all indicate that coal from the collier does not make a dominant contribution to any sediment sample. Mass balance calculations based on the n-C₂₄ content and 24/4 tetracyclic terpane to 26/3R tricyclic terpane ratio in coal provide a particularly good match between predicted and observed alkyl PAH concentrations for sediments with high alkyl naphthalenes and phenanthrene/anthracenes and low UCM, but the predicted coal contribution substantially underestimates the measured parent PAHs for all sediment samples. Methylbenz[a]anthracene/chrysene profiles for sediments with a dominance of parent PAHs are very close to coal tar, with a marked predominance of methylbenz[a]anthracenes and the possible 10-methylbenz[a]anthracene as a major constituent, while the methylchrysenes predominate in coal. Hence, coal from the collier could account for most alkyl PAHs in the sediments, but dredged sediment containing pyrolised coal waste from a former coal gas plant in Victoria Harbour is a more likely source for the samples with elevated parent PAHs. PAH ratios indicate that these sources are superimposed on combustion PAHs introduced by a combination of atmospheric deposition and delivery via stormwater and the outfalls. Parent PAH distributions also suggest that PAHs in wastewater that originate from oils and soot in liquid fossil fuel combustion are dispersed and degraded, while the larger wood char particles (containing PAHs more protected from degradation) settle closer to the outfalls. Overall, results suggest that PAHs have predominant sources in wood combustion, coal and possibly coke, with a likelihood of much lower bioavailability than would be expected from wastewater dominated by oils and soot from vehicle combustion.     

北京市表层土壤中PAHs含量特征及来源分析

土壤,作为城市中最重要的环境介质,承担了较高多环芳烃(PAHs)的环境负荷,开展土壤PAHs分布特征及来源分析研究,可以为污染风险防控、环保政策制定提供支撑.为研究北京市不同功能区土壤环境中PAHs的含量、组成及来源,本文在北京市主城区进行了大范围采样,同时针对工业区、农业种植区、水源保护区及居民区等不同功能区进行了分...