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1.
环境空气中多环芳烃(PAHs)不同岗位暴露情况研究   总被引:1,自引:0,他引:1  
孙华 《干旱环境监测》2006,20(4):207-210
探讨不同岗位暴露多环芳烃(PAHs)情况,结果表明,环境空气中PAHs受岗位影响显著,随暴露程度的加重,PAHs暴露浓度呈明显上升趋势。2、3环的PAHs主要分布在气相中,而4环以上的PAHs则主要存在于PM10中。PAHs相当于BaP当量致癌强度也表明,相对于气相来说,致癌源为PM10,其贡献率为90%。  相似文献   

2.
郑州市环境空气中多环芳烃污染状况及变化规律的研究   总被引:3,自引:1,他引:2  
对郑州市2004年环境空气中多环芳烃的污染状况及变化规律进行了初步研究,结果表明,郑州市环境空气中15种优控PAHs的浓度范围为未检出-698ng/m3,强致癌性物质苯并(a)芘的检出率为100%,其浓度范围为1.56~136ng/m3.PAHs类物质在不同季节的变化趋势为冬季>秋季>春季>夏季;在不同功能区变化趋势为工业区>混合区>交通密集区>文化区>对照区.  相似文献   

3.
2012年12月4日—11日,使用微孔均匀撞击式采样器(MOUDI)连续7 d采集广东省韶关市3个环境空气监测点气溶胶样品,采用GC/MS测定包括美国国家环保局(USEPA)优控多环芳烃(Σ16PAHs)在内的17种PAHs的浓度水平,并分析Σ16PAHs的粒径分布特征和来源。结果表明:韶关市冬季气溶胶颗粒中Σ16PAHs的质量浓度为17.29 ng/m3~23.97 ng/m3;Σ16PAHs集中在1.0μm~3.2μm的积聚态和粗颗粒中,呈单峰分布特征;比值参数分析显示,韶关市大气颗粒物中PAHs主要来自燃煤和汽车尾气的排放。  相似文献   

4.
采用紫外检测器和荧光检测器串联研究了测定碳素厂环境(废水、环境空气及烟道气)中多环芳烃(PAHs)的分析方法,一次进样可以同时获得紫外和荧光信号,具有更高的灵敏度和更好的选择性.  相似文献   

5.
对贵阳市不同功能区在不同季节大气PM_(2.5)中多环芳烃(PAHs)进行了采样观测,利用UVD和FLD双检测器串联HPLC法分析了16种优控PAHs。结果显示,在贵阳市主城区PM_(2.5)中PAHs有检出,5个采样点全年ρ(∑PAHs)为4. 44~114 ng/m~3,平均值为24. 96 ng/m~3,其值呈现出夏季最低冬季最高的特征,各个功能区在不同季节ρ(PAHs)不同,大小趋势也不同;四季PAHs单体中均以4-6环为主,占ρ(∑PAHs)的68%以上; PAHs来源解析结果显示,贵阳市大气PM_(2.5)中PAHs来源具有明显的季节特征,春、夏和秋季主要来源是石油燃烧排放,兼有少量的生物质燃烧排放,冬季PAHs主要来源是燃煤和石油燃烧排放。PM_(2.5)中PAHs毒性评价结果表明,贵阳市大气中PAHs的春季、夏季和秋季健康风险较小,冬季健康风险较大。四季各功能区ρ(Ba P)大部分均低于《环境空气质量标准》(GB 3095—2012)规定限值(2. 50 ng/m~3),但冬季除背景点外,其他监测点均超标,最大超标倍数为3. 80倍。  相似文献   

6.
采用自行研究制作的采样装置采集环境空气(包括气相和颗粒物)中的多环芳烃,用乙醚-正己烷混合溶剂提取,提取液经硅胶柱净化后,用液相色谱检测。并就PAHs在大气环境中的存在状态进行了研究。  相似文献   

7.
分析了隧道沥青摊铺过程环境空气中的TSP及多环芳烃质量浓度。TSP用膜法,中流量采样器采样15 min,重量法分析;超声波萃取,高效液相色法分析多环芳烃。结果表明,摊铺机周围空气中TSP超过8 mg/m3,道路空气中TSP超过3 mg/m3;环境空气中苊烯等12种多环芳烃均有检出,苊烯和艹屈质量浓度较高,苯并[a]芘和二苯并[a,h]蒽质量浓度较低。苯并[a]蒽、苯并[a]芘和二苯并[a,h]蒽超标,对人体健康危害较大。建议加强相关行业PAHs的排放水平及其健康风险研究,制定相关限值标准和沥青摊铺过程环境空气的沥青烟监测方法标准。  相似文献   

8.
对黑潴河下游表层沉积物中16种多环芳烃(PAHs)的污染现状进行了调查研究。结果表明,表层沉积物中PAHs总量变化范围为41.2~129.3ng/g(平均值为83.7ng/g),PAHs的组成以5~6环PAHs组分为主。黑潴河下游沉积物中PAHs主要来源于周边地区化石燃料的高温燃烧。比较了基于不同方法建立的沉积物中PAHs环境基准值的差异,分析产生差异的原因,选择生态效应区间法对黑潴河沉积物中的PAHs进行了生态风险评价。黑潴河下游PAHs生态风险较小,属PAHs低生态风险河道。  相似文献   

9.
概述了多环芳烃(PAHs)的属性和主要来源,介绍了其在不同环境介质中的分析方法、污染状况、迁移转化及风险评估现状,提出了进一步加强复杂环境基质中PAHs分析方法、不同环境介质中PAHs迁移转化特征,以及PAHs环境生态风险和人体健康风险等方面研究的建议。  相似文献   

10.
对2012年郑州市大气中气态和颗粒态多环芳烃(PAHs)的分布特征与来源进行了分析。结果表明,ρ(∑PAHs)(包括气相与颗粒相)为23.27~194.61 ng/m3,气相中∑PAHs高于颗粒相,四环以下的PAHs大都存在于气态中;在夏、春2季,较小分子质量(≤178)的PAHs占比较高,冬季,较大分子质量(≥252)的PAHs占比明显较高;各功能区ρ(PAHs)排序为工业区交通密集区医疗、文化、行政混合区。郑州大气和颗粒物中PAHs可能主要来自煤和液体燃料(汽油柴油)的燃烧。  相似文献   

11.
气溶胶与降尘中多环芳烃的含量分布研究   总被引:13,自引:1,他引:12  
通过广东省茂名市区四个不同功能点大气气溶胶和降尘中多环芳烃的含量分布研究发现 :1、气溶胶中优控多环芳烃大大高于降尘中的含量 ,为降尘的 5.97~ 1 9.3倍 ;以石化厂区为例 ,非优控多环芳烃在气溶胶中的相对含量更高 ,为降尘的 2 4 .7倍。2、气溶胶中优控多环芳烃和非优控多环芳烃的分布为随分子量增加而含量增高的趋势 ,但降尘中优控多环芳烃的高含量相对集中于萤蒽至苯并 (b)萤蒽之间。3、不同功能区由于排放源的差别所表现出的气溶胶和降尘中优控多环芳烃总量及总量比值、部分强致癌和致癌物含量及含量比值均存在差异。4、对气溶胶和降尘中多环芳烃研究可以对降尘中非优控多环芳烃降解和溶解量进行估算。以石化厂区为例 ,降尘中非优控多环芳烃比原始含量已减少76%。  相似文献   

12.
The concentrations, distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in 30 agricultural soil and 16 vegetable samples collected from subtropical Shunde area, an important manufacturing center in China. The total PAHs ranged from 33.7 to 350 μg/kg in soils, and 82 to 1,258 μg/kg in vegetables. The most abundant individual PAHs are phenanthrene, fluoranthene, chrysene, pyrene and benzo(b)fluoranthene for soil samples, and anthracene, naphthalene, phenanthrene, pyrene and chrysene for vegetable samples. Average vegetable–soil ratios of total PAHs were 2.20 for leafy vegetables and 1.27 for fruity vegetables. Total PAHs in vegetable samples are not significantly correlated to those in corresponding soil samples. Principal component analyses were conducted to distinguish samples on basis of their distribution in each town, soil type and vegetable specie. Relatively abundant soil PAHs were found in town Jun’an, Beijiao, Chencun, Lecong and Ronggui, while abundant vegetable PAHs were observed in town Jun’an, Lecong, Xingtan, Daliang and Chenchun. The highest level of total PAHs were found in vegetable soil, followed by pond sediment and “stacked soil” on pond banks. The PAHs contents in leafy vegetables are higher than those in fruity vegetables. Some PAH compound ratios suggest the PAHs derived from incomplete combustion of petroleum, coal and refuse from power generation and ceramic manufacturing, and paint spraying on furniture, as well as sewage irrigation from textile industries. Soil PAHs contents have significant logarithmic correlation with total organic carbon, which demonstrates the importance of soil organic matter as sorbent to prevent losses of PAHs.  相似文献   

13.
The level, distribution, compositional pattern, and possible sources of polycyclic aromatic hydrocarbons (PAHs) in agricultural soil of Shanghai were investigated. The concentrations ranged from 140.7 to 2,370.8 μg kg(?-1) for 21 PAHs and from 92.2 to 2,062.7 μg kg(?-1) for 16 priority PAHs, respectively. The higher level of PAHs was mainly distributed in the south and west of Shanghai region, and the lower concentration was found in Chongming Island. Generally, the composition pattern of PAHs was characterized with high molecular weight PAHs, the seven possible carcinogenic PAHs accounted for 4.8-50.8% of the total PAHs, and fluoranthene, pyrene, and benzo[b]fluoranthene were the most dominant components in soil samples. The correlation analysis suggested that low molecular weight PAHs and high molecular weight PAHs were originated from different sources and further corroborated that total organic carbon was a key soil property affecting the fate of persistent organic pollutants in the environment. The isomer ratios and principal component analysis indicated that PAHs in the investigated areas were derived primarily from combustion of biomass, coal, and petroleum. Compared to the soil quality standards of the Netherlands, all the target PAHs (except Ant) in most samples exceeded their target values. The Nemerow composite index based on the same soil quality standard showed that 69.4% of the soil samples were heavily polluted. The total BaP(eq) of ten Dutch target PAHs in 72% soil samples were higher than the reference total carcinogenic potency. Therefore, the agricultural soil in Shanghai is suffering from serious PAHs contamination.  相似文献   

14.
Polycyclic aromatic hydrocarbons (16 EPA-PAHs) in urban surface soil from Jiaxing City were determined using HPLC. The total concentration of 16 EPA-PAHs was detected from 18.73 to 441.34 pg/g. Individual PAH occupation analysis demonstrates that four-ring PAHs comprise as much as 44.16% and were prevalent in the composition of PAH pollutants. The other components were two-ring PAHs (7.36%), three-ring PAHs (17.28%), five-ring PAHs (16.16%), and six-ring PAHs (15.04%). Source analysis on the characteristic ratios of anthracene(Ane)/[Ane+phenanthrene(Phe)], fluoranthene(Fla)/[Fla+pyrene(Pyr)], and benzo[a]pyrene(Bap)/benzo[g,h,i]perylene(Bgp) reveals that PAH pollutants originated mainly from coal combustion, but vehicular emission as a source was not negligible. All PAHs discussed in the paper have similar source in most sampling sites. The spatial distributions of pollution sources were closely related to geographic location, geographic condition, and living habit of indigenes. A linear relationship between 2-3-ring PAHs, 4-6-ring PAHs, SOM, and ∑PAHs were investigated and significant correlativity were expatiated lastly. It revealed that coefficient between 2-3-ring PAHs and ∑PAHs is 0.56, between 4-6-ring PAHs and ∑PAHs is 0.99, between SOM and ∑PAHs is 0.82.  相似文献   

15.
Air pollution has become a serious problem in the Pearl River Delta, South China, particularly in winter due to the local micrometeorology. In this study, atmospheric polycyclic aromatic hydrocarbons (PAHs) were monitored weekly in Shenzhen during the winter of 2006. Results indicated that the detected PAHs were mainly of vapor phase compounds with phenanthrene dominant. The average vapor phase and particle phase PAHs concentration in Shenzhen was 101.3 and 26.7 ng m???3, respectively. Meteorological conditions showed great effect on PAH concentrations. The higher PAHs concentrations observed during haze episode might result from the accumulation of pollutants under decreased boundary layer, slower wind speed, and long-term dryness conditions. The sources of PAHs in the air were estimated by principal component analysis in combination with diagnostic ratios. Vehicle exhaust was the major PAHs source in Shenzhen, accounting for 50.0% of the total PAHs emissions, whereas coal combustion and solid waste incineration contributed to 29.4% and 20.6% of the total PAHs concentration, respectively. The results clearly indicated that the increasing solid waste incinerators have become a new important PAHs source in this region.  相似文献   

16.
于非采暖季和采暖季分别采集某石化化工行业聚集城市中心城区室内外PM_(2.5)样品,采用高效液相色谱法分析PM_(2.5)上载带的16种PAHs,对其分布特征、来源以及室外PAHs污染对室内污染的贡献进行了初步探讨。结果表明,研究区域非采暖季和采暖季室外PM_(2.5)中ΣPAHs浓度日均值分别为36.3、294 ng/m~3,室内PM_(2.5)中ΣPAHs浓度分别为14.8、84.6 ng/m~3,均以4、5环PAHs为主;室内PAHs主要来自室外渗透污染,但同时明显存在室内排放源贡献;PAHs来源分析进一步证实研究区域PAHs主要来自煤炭、石油等不完全燃烧,采暖季煤炭燃烧源贡献更突出。  相似文献   

17.
This study reports source apportionment of polycyclic aromatic hydrocarbons (PAHs) in particulate depositions on vegetation foliages near highway in the urban environment of Lucknow city (India) using the principal components analysis/absolute principal components scores (PCA/APCS) receptor modeling approach. The multivariate method enables identification of major PAHs sources along with their quantitative contributions with respect to individual PAH. The PCA identified three major sources of PAHs viz. combustion, vehicular emissions, and diesel based activities. The PCA/APCS receptor modeling approach revealed that the combustion sources (natural gas, wood, coal/coke, biomass) contributed 19–97% of various PAHs, vehicular emissions 0–70%, diesel based sources 0–81% and other miscellaneous sources 0–20% of different PAHs. The contributions of major pyrolytic and petrogenic sources to the total PAHs were 56 and 42%, respectively. Further, the combustion related sources contribute major fraction of the carcinogenic PAHs in the study area. High correlation coefficient (R 2 > 0.75 for most PAHs) between the measured and predicted concentrations of PAHs suggests for the applicability of the PCA/APCS receptor modeling approach for estimation of source contribution to the PAHs in particulates.  相似文献   

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