燃煤电厂多环芳烃的生成与控制

多环芳烃（PAHs)对人体健康的危害极大。本文综述了燃煤电厂煤燃烧过程中多环芳烃的生成机理（直接释放，热解合成和高温缩合机理）和影响因素（煤种，温度，锅炉负荷，过剩空气系数，停留时间，钙硫比和一次风/二次风比）。在此基础上介绍了煤燃烧过程中多环芳烃的各种控制技术和方法。     

北方某城市饮用水中多环芳烃的来源及其在水处理过程中的行为研究

采用固相萃取(SPE)样品富集前处理技术和气相色谱/质联联用(GC/MS)分析方法,对北方某工业城市给水系统中的多环芳烃类化合物的含量水平进行了研究.结果表明,该城市多环芳烃污染水平较高,但总浓度均未超过城市供水水质标准(CJ/T206-2005)中限值(2μg/L).近郊水库由于受到燃料燃烧产生的多环芳烃的污染,成为该市饮用水中多环芳烃污染的主要来源.传统的混凝-砂滤工艺对多环芳烃有较好的去除效果,总去除率可达55.9%.     

石家庄市大气环境苯并(a)芘污染初步研究

苯并(a)芘(BaP)是多环芳烃类化合物(PAN),是环境中普遍存在的一种致癌性很强的物质.主要来源于含碳燃料和一些有机物的热解过程或不完全燃烧过程.我国城市的BaP现状浓度是较高,主要与能源结     

中国南方某城市自来水厂处理工艺对多环芳烃的去除效果研究

讨论了中国南方某城市自来水厂饮用水中的多环芳烃残留规律以及现有净水工艺对多环芳烃的去除效果。研究结果表明,该自来水厂饮用水中检出多环芳烃以2~4环芳烃为主,强致癌性高环数多环芳烃均在检出限以下,且多环芳烃总量未超出中国供水行业标准(2000年)的相关限值。各处理工艺段中,砂滤过程对多环芳烃的去除效果最好,相较于原水对多环芳烃总量的去除率可达64%。     

中国南方某城市自来水厂处理工艺对多环芳烃的去除效果研究

讨论了中国南方某城市自来水厂饮用水中的多环芳烃残留规律以及现有净水工艺对多环芳烃的去除效果。研究结果表明，该自来水厂饮用水中检出多环芳烃以2～4环芳烃为主，强致癌性高环数多环芳烃均在检出限以下，且多环芳烃总量未超出中国供水行业标准(2000年)的相关限值。各处理工艺段中，砂滤过程对多环芳烃的去除效果最好，相较于原水对多环芳烃总量的去除率可达64％。     

峰峰矿区奥灰水多环芳烃组成、分布特征及其来源

为分析峰峰矿区煤矿开采后矿区地下水多环芳烃(PAHs)的分布和来源,在矿区采集并分析了15件奥灰水样品,对样品中16种PAHs的含量进行统计分析,并运用氢氧同位素和同分异构体比值相结合的方法分析确定了其污染来源。结果表明:峰峰矿区奥灰水中PAHs总质量浓度为0.06~0.56ng/L,呈现出萘(Nap)、菲(Phe)、蒽(Ant)、荧蒽(Flt)、芘(Pyr)、芴(Flu)为主的2~4环PAHs低浓度高检出特征;Ant/(Ant+Phe)—Flt/(Flt+Pyr)结果表明奥灰水中PAHs主要来自煤和生物质的燃烧;δD—δ18 O、δD—Phe结果表明,奥灰水中的PAHs主要来源于煤和生物质燃烧产物在高海拔基岩裸露地区随降雨直接入渗补给;少数来源于潜水、矿井水和煤系基岩水等的越流补给。     

蜂窝煤燃烧烟气中多环芳烃的定量研究及粒径分布特征

通过对蜂窝煤燃烧排放的烟气中多环芳烃的定量分析,研究了17种多环芳烃在烟气颗粒相和气相中的分配以及在不同粒径颗粒物上的分布特征。结果表明：在室温下燃煤排放的多环芳烃总量以在气相中存在为主,但总体毒性则主要存在于颗粒相中;多环芳烃主要分布在亚微米级颗粒上,分子量越大的多环芳烃越趋于富集在细颗粒上,因而对健康的危害就越大。     

中国年燃煤会释放5亿t多环芳烃?

<正>近日,有报道称,一吨燃煤在燃烧过程中会释放300kg的多环芳烃。那么,按照2015年我国消耗煤炭量为36.98亿t计算,多环芳烃每年的释放量高达约5.55亿t。中国科学院院士、北京大学教授陶澍带领的团队长期从事多环芳烃排放清单的研究,他对这个报道进行了辟谣"这     

南京市气溶胶PM2.5中多环芳烃来源识别

对2005年7月至2006年2月采集到的南京市气溶胶Pm2.5 进行季节性初步分析,并对其中的15种优控多环芳烃(PAHs)进行分析研究,通过比值法判断南京市PAHs夏季主要来源于柴油型燃烧,冬季主要来源于柴油和煤型相结合的燃烧.对15种优控PAHs两两之间的相关性分析,发现各化合物之间显著相关,表明各化合物的来源有相似之处.     

多环芳烃在低氧沉积物环境中的分布状况

低氧环境普遍存在于底层水体以及表层沉积物中,随着中国水体有机污染加剧,低氧现象将越来越明显.有研究表明,中国水体普遍受到多环芳烃污染,由于其强烈的憎水性和低溶解性,大部分多环芳烃沉积在底泥中.总结了学者们对国内外河流、湿地、河口等水体沉积物中多环芳烃污染的研究成果,探讨了多环芳烃的分布规律,发现沉积物中多环芳烃含量与流域内经济发展状况密切相关,反映了经济发展过程对环境造成的负面影响.相比于国外典型区域的多环芳烃浓度,中国沉积物的多环芳烃污染处于中等水平,但处于快速上升阶段,部分点位浓度已超过生态风险区间低值(4 000 ng/g),对人们的身体健康构成威胁,所以对多环芳烃的生态风险评价、污染物排放控制需进一步加强.     

Characterization and source identification of polycyclic aromatic hydrocarbons (PAHs) in the urban environment of Delhi

This paper reports on polycyclic aromatic hydrocarbons (PAHs) in the atmospheric particulate matter of Jawaharlal Nehru University campus, an urbanized site of New Delhi, India. Suspended particulate matter samples of 24h duration were collected on glass-fiber filter paper for four representative days in each month during January 2002 to December 2003. PAHs were extracted from filter papers using toluene with ultrasonication method and analysed. Quantitative measurements of polycyclic aromatic hydrocarbons (PAHs) were carried out using the gas chromatography technique. The annual average concentration of total PAHs were found to be 668+/-399 and 672+/-388 ng/m3 in the years 2002 and 2003, respectively. The seasonal average concentrations were found to be maximum in winter and minimum during in the monsoon. The results of principal component analysis (PCA) indicate that diesel and gasoline driven vehicles are the principal sources of PAHs in all the seasons. In winter coal and wood combustion also significantly contribute to the PAH levels.     

A study of polycyclic aromatic hydrocarbons concentrations and source identifications by methods of diagnostic ratio and principal component analysis at Taichung chemical Harbor near Taiwan Strait

Fine (PM(2.5)) and Coarse (PM(2.5-10)) particulates concentrations of ambient air particle-bound polycyclic aromatic hydrocarbons (PAHs) were measured simultaneously from February 2004 to January 2005 at the Taichung Harbor (TH) sampling site near Taiwan of central Taiwan. Particle-bound polycyclic aromatic hydrocarbons (PAHs) were collected on quartz filters, the collected sample used soxhlet analytical method extracted with a dichloromethane (DCM)/n-hexane mixture (50/50, v/v) for 24h, and then the extracts were subjected to gas chromatography-mass spectrometric (GC-MS) analysis. The results indicated that vehicle emissions, coal combustion, incomplete combustion and pyrolysis of fuel and oil burning were the main source of PAHs near Taiwan Strait of central Taiwan. Diagnostic ratio and principal component analysis (PCA) were also used to characterize and identify PAHs emission source in this study.     

Effect of copper chloride on the emissions of PCDD/Fs and PAHs from PVC combustion

The influences of temperature, air flow and the amount of copper chloride upon the types and amount of the toxic emissions such as polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) and polycyclic aromatic hydrocarbons (PAHs) during combustion of polyvinyl chloride (PVC) were investigated. The mechanism concerning the effect of temperature and copper chloride on the PCDD/Fs and PAHs formation was discussed. The results shown that without copper chloride, trace amounts of PCDD/Fs and large amounts of PAHs were found in the emissions from the pure PVC combustion under various combustion conditions. The addition of copper chloride enhanced PCDD/Fs formation, but it seems that the formation of PAHs decreased with increasing amount of copper chloride, and greater total amount of PAHs were produced at the higher temperature under our experimental conditions.     

Compounds in Airborne Participates: Salts and Hydrocarbons

Concentrations of 10 polycyclic aromatic hydrocarbons (PAH), the aliphatlcs as a group, sulfate, nitrate, fluoride, acidity, and carbon In the airborne partlculate matter were measured at 16 sites In Cleveland, OH over a 1 year period during 1971 and 1972. Analytical methods used included gas chromatography, colorimetry, and combustion techniques. Uncertainties in the concentrations associated with the sampling procedures, and the analytical methods are evaluated. The data are discussed relative to other studies and source origins. Benzo(a)pyrene and its high concentrations downwind of coke ovens are discussed. Hydrocarbon correlation studies indicated no significant relations among compounds studied.     

Emission factors of particulate matter,polycyclic aromatic hydrocarbons,and levoglucosan from wood combustion in south-central Chile

In south-central Chile, wood stoves have been identified as an important source of air pollution in populated areas. Eucalyptus (Eucalyptus globulus), Chilean oak (Nothofagus oblique), and mimosa (Acacia dealbata) were burned in a single-chamber slow-combustion wood stove at a controlled testing facility located at the University of Concepción, Chile. In each experiment, 2.7–3.1 kg of firewood were combusted while continuously monitoring temperature, exhaust gases, burn rate, and collecting particulate matter samples in Teflon filters under isokinetic conditions for polycyclic aromatic hydrocarbon and levoglucosan analyses. Mean particulate matter emission factors were 2.03, 4.06, and 3.84 g/kg dry wood for eucalyptus, oak, and mimosa, respectively. The emission factors were inversely correlated with combustion efficiency. The mean emission factors of the sums of 12 polycyclic aromatic hydrocarbons in particle phases were 1472.5, 2134.0, and 747.5 μg/kg for eucalyptus, oak, and mimosa, respectively. Fluoranthene, pyrene, benzo[a]anthracene, and chrysene were present in the particle phase in higher proportions compared with other polycyclic aromatic hydrocarbons that were analyzed. Mean levoglucosan emission factors were 854.9, 202.3, and 328.0 mg/kg for eucalyptus, oak, and mimosa, respectively. Since the emissions of particulate matter and other pollutants were inversely correlated with combustion efficiency, implementing more efficient technologies would help to reduce air pollutant emissions from wood combustion.

Implications: Residential wood burning has been identified as a significant source of air pollution in populated areas. Local wood species are combusted for home cooking and heating, which releases several toxic air pollutants, including particulate matter, carbon monoxide, and polycyclic aromatic hydrocarbons. Air pollutant emissions depend on the type of wood and the technology and operational conditions of the wood stove. A better understanding of emissions from local wood species and wood stove performance would help to identify better biomass fuels and wood stove technologies in order to reduce air pollution from residential wood burning.     

The phototoxicity of non-carcinogenic polycyclic aromatic hydrocarbons in aquatic organisms

Anthracene, fluoranthene, and pyrene are phototoxic in , first instar larvae of , late embryonic forms of , and fish ( ). Since polycyclic aromatic hydrocarbons are generated in the combustion processes held responsible for the damages of acid rain, and they are introduced into the environment through other means as well, the high phototoxicity of the major pollutants, which are not carcinogenic, suggests that greater attention must be given to their environmental significance.     

Investigation of aqueous solubilities of nitro-PAH by dynamic couple-column HPLC

A dynamic couple-column high performance liquid chromatographic technique was used to determine the aqueous solubilities of 9 nitrated polycyclic aromatic hydrocarbons. A linear relationship between aqueous solubilities and molecular connectivity indices of these compounds has been established. According to this relationship, the aqueous solubilities of 18 other nitrated polycyclic aromatic hydrocarbons were estimated.     

Characteristic study of polycyclic aromatic hydrocarbons for fine and coarse particulates at Pastureland near Industrial Park sampling site of central Taiwan

The concentrations of ambient air polycyclic aromatic hydrocarbons were measured in a farm area (Tunghai University Pastureland) between August 2001 and April 2002 in central Taiwan, Taichung. Particle-bound polycyclic aromatic hydrocarbons (PAHs) were collected on quartz filters, the collected sample was extracted with a dichloromethane (DCM)/n-hexane mixture (50/50, v/v) for 24 h, and then the extracts were subjected to gas chromatography-mass spectrometric analysis. The PM2.5 (fine particulate) and PM2.5-10 (coarse particulate) total PAHs concentrations at the Tunghai University Pastureland sampling site were found to be 180.62 ngm(-3) and 164.98 ngm(-3), respectively. In general, the concentrations of polycyclic aromatic hydrocarbons were higher in spring and winter than those of summer and autumn for either PM2.5 or PM2.5-10 in Pastureland in central Taiwan. Moreover, coarse particulates are the dominant species during the dust storm season (March and April) in central Taiwan.     

Temporal trends of hydrocarbons in sediment cores from the Pearl River Estuary and the northern South China Sea

Concentrations and fluxes of unresolved complex mixture of hydrocarbons (UCM) and polycyclic aromatic hydrocarbons (PAHs) were analyzed for two ²¹⁰Pb dated sediment cores from the Pearl River Estuary (PRE) and the adjacent northern South China Sea (NSCS). Compound-specific stable carbon isotopic compositions of individual n-alkanes were also measured for identification of the hydrocarbon sources. The historical records of PAHs in the NSCS reflected the economic development in the Pearl River Delta during the 20th century. PAHs in the NSCS predominantly derive from combustion of coal and biomass, whereas PAHs in the PRE are a mixture of petrogenic and pyrogenic in origins. The isotopic profiles reveal that the petrogenic hydrocarbons in the PRE originate predominantly from local spillage/leakage of lube oil and crude oils. The accumulation rates of pyrogenic PAHs have significantly increased, whereas UCM accumulation has slightly declined in the NSCS in the recent three decades.     

On the aliphatic,and polycyclic aromatic hydrocarbon levels in the southern baltic sea atmosphere

Samples of marine aerosols from the S Baltic Sea have been analysed for aliphatic hydrocarbons from pentadecane to dotriacontane, and for polycyclic aromatic hydrocarbons (PAHs) from anthracene and phenantrene to benzo(ghi)perylene. Some of the sampling stations were situated near industrialized areas (Gdańsk Bay, Pommeranian Bay) and some others in the open Baltic Sea. The aliphatic hydrocarbons were analysed by gas chromatography, polycyclic aromatic hydrocarbons by HPLC. Quantitative composition of the hydrocarbons in the Baltic aerosols is presented and discussed.