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1.
采用固相萃取-GC/MS法分析海河流域9个典型地表水水源地16种多环芳烃(PAHs)污染状况,结果显示除BkFL、BaP、InP、BghiP和DBA未检出外,其他11种PAHs均有检出。9个水源地春季水体中PAHs总值为238 ng/L~715 ng/L,夏季水体中PAHs总值为837 ng/L~278 ng/L, 表明PAHs季节性污染差异较为显著,夏季PAHs污染状况明显高于春季。PAHs的组成均以中低环芳烃(2~3环)为主,且Ant/(Phe+Ant)、Flu/(Pyr+Flu)和BaA/(BaA+Chr)比值显示9个水源地PAHs污染均来源于水源地上游煤炭、木材等燃烧产物。  相似文献   

2.
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   

3.
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   

4.
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   

5.
筛选识别成都市多环芳烃(PAHs)污染重点源和区域,采集57个土壤样品,利用人体暴露风险模型对16种PAHs的健康风险进行评价。结果表明:青白江工业集中发展区与新都工业集中发展区连片区局部有PAHs潜在渗漏风险,污染源主要为工业企业和交通源,农业面源、生活污染源等不直接产生PAHs;土壤PAHs主要来源途径为企业VOCs排放与沉降、汽车尾气与大气中PAHs沉降、废矿物油泄漏入渗;PAHs主要离去途径为入渗地下水、冲淋径流进入地表水、植物吸收;智能设备制造、化工用地存在PAHs人体健康及环境生态风险。  相似文献   

6.
综述了近年来我国大气、水、土壤环境和生态系统中多环芳烃(PAHs)污染状况研究进展,指出化石燃料及其衍生物的燃烧产物是PAHs的主要来源,虽然我国大部分地区生态环境中PAHs风险较低,但仍须关注其潜在的健康风险,提出多学科交叉研究典型PAHs在生态系统中的环境行为及原位修复技术等未来研究方向。  相似文献   

7.
珠江口表层水中多环芳烃的分布特征及健康风险评估   总被引:1,自引:0,他引:1  
分别于2015年2、5、8、11月在珠江八大入海口采集表层水体样品,应用固相萃取富集法对该区域表层水体中16种USEPA优控多环芳烃(PAHs)的时空分布特征进行分析,并利用终生致癌风险增量模型(ILCR)对该区域的饮水健康风险进行评价。结果表明:珠江口4个季度所采集的水样中,∑15PAHs的浓度范围为18.0~50.3 ng/L,含量处于中等水平。其中7种强致癌性∑7PAHs的浓度范围为1.53~3.73 ng/L,占∑15PAHs的5.89%~11.1%,∑15PAHs和∑7PAHs在枯水期(2、11月)样品中明显高于丰水期(5、8月)。就组成特征而言,各采样点PAHs以3、4环为主。珠江口表层水中非致癌类PAHs的危害商数值为0.99×10~(-5)~2.73×10~(-5),远低于USEPA规定的阈值(1);致癌类PAHs产生的健康风险为6.50×10~(-8)~2.37×10~(-7),其中Ba P导致的饮水途径健康风险最高,所有点位致癌类PAHs的健康风险均低于USEPA推荐的对致癌物质最大可接受风险水平(10~(-6)),表明珠江口表层水中PAHs尚不具备严重的致癌风险,但是仍然存在潜在的健康风险,需要重点控制和管理。  相似文献   

8.
多环芳烃(PAHs)是一类极其复杂的有机污染物,衍生物种类较多,1976年美国环保局因其致癌、致畸、致突变将其中的16种列为优先控制污染物。城市污水处理厂作为一个地区污染物迁移和转化的重要媒介,在控制和截断PAHs进入天然水体的过程中扮演着重要的角色。因此,研究污水处理厂中PAHs的浓度水平对于了解和控制PAHs进入天然水体和通过污泥进入到土壤中进而通过食物链危害人类健康具有重要的意义。文章综述了污水处理厂污水和污泥中PAHs的前处理技术、分析方法、浓度水平、生态风险以及国内外污水处理厂污泥土地利用现状。  相似文献   

9.
环境中多环芳烃前处理和分析方法   总被引:2,自引:1,他引:1       下载免费PDF全文
多环芳烃(PAHa)是一类广泛存在于大气、水体、土壤、沉积物中的持久性有机污染物,对环境和生物体存在较大危害.介绍了国内外部分水体中PAHs的污染状况,对液态和固体PAHs的主要前处理方法和分析方法进行了比较和归纳,展望了环境样品中PAHs的前处理和分析方法的发展方向.  相似文献   

10.
利用气相色谱-质谱联用仪(GC-MS)对广西清水泉地下河水16种多环芳烃(PAHs)的质量浓度进行了测定,研究地下河水中PAHs的质量浓度、组成和分布,并对其进行生态风险评价,为城市近郊型地下河系统持久性污染物防治提供科学依据。结果表明,地下河水中∑PAHs质量浓度为162.13~224.99 ng/L,平均值为191.71 ng/L,PAHs以2~3环为主,占49.36%;地下河水中PAHs的质量浓度自上游至下游逐渐增大,2~3环PAHs的百分比先升高后降低;地下河水中Ba A和Bb F处于中等污染和高污染风险,应采取控制或修复措施降低污染风险,剩余PAHs除了In P在水中未检出外,均显示为低污染风险。  相似文献   

11.
The Songhua River is the third largest river in China and the primary source of drinking and irrigation water for northeastern China. The distribution of 16 priority polycyclic aromatic hydrocarbons (PAHs) in water [dissolved water (DW) and suspended particulate matter (SPM)], sediment, and soil in the river basin was investigated, and the associated risk of cancer from these PAHs was also assessed. The total concentration of PAHs ranged from 13.9 to 161 ng L?1 in DW, 9.21 to 83.1 ng L?1 in SPM, 20.5 to 632 ng g?1 dw (dry weight) in sediment, and from 30.1 to 870 ng g?1 dw in soil. The compositional pattern of PAHs indicated that three-ring PAHs were predominant in DW and SPM samples, while four-ring PAHs dominated in sediment and soil samples. The spatial distribution of PAHs revealed some site-specific sources along the river, with principal component analysis indicating that these were from pyrogenic sources (such as coal and biomass combustion, and vehicle emissions) and coke oven emission distinguished as the main source of PAHs in the Songhua River Basin. Based on the ingestion of PAH-contaminated drinking water from the Songhua River, cancer risk was quantitatively estimated by combining the Incremental Lifetime Cancer Risk assessment model and BaP-equivalent concentration for five age groups of people (adults, teenagers, children, toddlers, and infants). Overall, the results suggest that the estimated integrated lifetime cancer risk for all groups was in acceptable levels. This study is the first attempt to provide information on the cancer risk of PAHs in drinking water from the Songhua River.  相似文献   

12.
为研究庞庄煤矿张小楼煤矸石堆场淋溶液对其场地和周边地表水、地下水水质影响情况,围绕煤矸石堆场及周边采集13组水样做分析比对。结果表明,煤矸石堆场淋溶液对周边地表水体形成普遍污染,且污染物浓度随着污染距离增加逐步降低,一般化学污染指标主要包括溶解性总固体、硫酸盐、铁、锰、氨氮等,毒理学污染指标包括亚硝酸盐、氟化物、砷,超标倍率约为0.02~5.36。受距离及成井深度等因素影响,地下水体未遭受淋溶液明显的污染和影响。  相似文献   

13.
Polycyclic aromatic hydrocarbons (PAHs) are important organic contaminants with great significance for China, where coal burning is the main source of energy. In this study, concentrations, distribution between different phases, possible sources and eco-toxicological effect of PAHs of the Yangtze River were assessed. PAHs in water, suspended particulate matters (SPM) and sediment samples at seven main river sites, 23 tributary and lake sites of the Yangtze River at the Wuhan section were analyzed. The total concentrations of PAHs in the studied area ranged from 0.242 to 6.235 μg/l in waters and from 31 to 4,812 μg/kg in sediment. The average concentration of PAHs in SPM was 4,677 μg/kg, higher than that in sediment. Benzo(a)pyrene was detected only at two stations, but the concentrations were above drinking water standard. The PAHs level of the Yangtze River was similar to that of some other rivers in China but higher than some rivers in foreign countries. There existed a positive relationship between PAHs concentrations and the TOC contents in sediment. The ratio of specific PAHs indicated that PAHs mainly came from combustion process, such as coal and wood burning. PAHs may cause potential toxic effect but will not cause acute biological effects in sedimentary environment of the Wuhan section of the Yangtze River.  相似文献   

14.
2011年4月通过GC-MS检测和210Pb测年对灌河口海域沉积物(GHES)中的PAHs进行了分析,柱状沉积物中21种PAHs总浓度为21.0~209.0 ng/g,均值为88.1 ng/g,7种致癌PAHs浓度为7.0~90.0 ng/g,其中致癌剂苯并[a]芘浓度为ND~2.0 ng/g。PAHs浓度与沉积物中有机质含量呈低度正相关,与p H无明显相关性。源解析表明,近50年来GHES中的PAHs大部分来自煤和生物质燃烧。近50年来,总PAHs和16种优控PAHs浓度在波动中升高;近年来苊、苊烯、苯并[b]荧蒽、荧蒽、茚并[1,2,3-cd]芘的浓度增高,需查明来源。生态风险评价表明,GHES中以芴为主的负面生物毒性效应会偶尔发生。芴、苯并[b]荧蒽、苯并[k]荧蒽的浓度介于临界与偶然效应浓度值之间,应尽量减少对该海域沉积物的搅动,防止污染物再悬浮导致水体的二次污染。  相似文献   

15.
利用自制被动采样装置,在2011年秋冬季对南京市部分地区室内空气中5种气态多环芳烃(PAHs)(萘、苊烯、苊、芴、菲)进行了为期100d的连续采样检测,被动采样器的采样速率为0.012m3/d,5种PAHs的回收率在63%~105%之间,方法检出限在1.1~2.4ng范围内。结果表明,南京市5处不同室内环境空气中萘的浓度最高,占总量的90%以上。室内环境空气中5种PAHs的总浓度为230~1564ng/m3。住宅内人体对5种PAHs的暴露速率为479~560ng/h。  相似文献   

16.
Distribution and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in drinking water resources have been carried out for the first time in Henan Province, China. Water samples collected from four river systems and their tributaries, as well as groundwater resources, were analyzed according to EPA method 525.2. Total of 68 water samples were collected in 18 cities in Henan province in May, August and November, 2001. Concentrations of sum of 16 priority PAHs in water samples ranged from 15 to 844 ng/L with a mean value of 178 +/- 210 ng/L (n = 68). The spatial and temporal distribution of PAHs showed that the Huanghe and the Huaihe river systems had relatively higher concentrations of total PAHs. Higher concentrations of total PAHs were observed in August and November than in May, with respective mean values of 262, 232 and 33.6 ng/L. Ratios of Ant/(Ant + Phe) and Flur/(Flur + Pyr) were calculated to evaluate the possible sources of PAH contamination, which indicated that the coal combustion sources were the main contributors to PAHs in most drinking water resources. Some petrogenic (or pyrolytic) sources of PAHs were also found. The toxic equivalency factors (TEFs) were used to calculate benzo[a]pyrene equivalents (BaPE) for water samples. The average value of BaPE was 0.6 ng/L. The values in most stations were much lower than the guideline values in drinking water of Chinese Environmental Protection Agency (CEPA, 2.8 ng/L) and the US Environmental Protection Agency (US EPA, 200 ng/L). Overall, the drinking water resources in Henan province showed some carcinogenic potential.  相似文献   

17.
乌鲁木齐地表水饮用水源地水体有机氯农药健康风险评价   总被引:1,自引:0,他引:1  
为了解乌鲁木齐市地表饮用水源地水体中有机氯农药(OCPs)对人体产生的潜在健康危害风险,从一号冰川、英雄桥、乌拉泊水库的9个采样点采集水样,采用液液萃取-气相色谱/质谱法对其中的有机氯农药残留状况进行了测定,水样中9种有机氯化合物的总质量浓度为15.1 ng/L~41.2 ng/L。应用美国国家环保局(US EPA)推荐的健康风险评价方法,对乌鲁木齐市地表饮用水源地水体中有机氯农药通过食用途径进入人体的危害进行了风险计算和初步评价。结果表明,各监测断面的致癌风险和非致癌风险低于ICRP和USEPA推荐的最大可接受风险水平,初步认为目前乌鲁木齐市地表饮用水源地水体中有机氯农药不会对人体产生明显的健康危害。  相似文献   

18.
Sources, partitioning and toxicological risk of 15 priority polycyclic aromatic hydrocarbons (PAHs) in surface sediments from drinking water sources of Taihu Lake, with an area of 2428 km(2) located in the most developed and populated area of China, were studied, and the results were compared with those in other lakes of China and the USA. Concentrations of the 15 PAHs in sediments ranged from 436.6 to 1334.9 ng g(-1) (dw). Gasoline combustion, coal combustion, diesel combustion from shipping and spillage of petroleum were apportioned to be the main sources of PAHs in this area by principal component analysis, which contributed 35.19%, 26.43%, 25.41% and 12.97% to the PAH sources estimated by further multiple linear regression. Levels of PAHs in sediments were negatively correlated with contents of clay and fine silt (<16 μm), while positively with contents of medium silt, coarse silt and sand (>16 μm). Humin with size larger than 16 μm contained the largest part of the burden of PAHs in sediments, but the specific partitioning domain (bound humic acid, lipid or insoluble residue) depended on properties of organic matter reflected by optical absorbance at 465 and 665 nm. Total toxic benzo[a]pyrene equivalent (TEQ(carc)) of the carcinogenic PAHs in sediments varied from 31.8 to 209.3 ngTEQ(carc) g(-1). Benzo[a]pyrene and dibenzo[a,h]anthracene contributed 45.36 and 25.31% to total TEQ(carc), posing high toxicological risk to this area.  相似文献   

19.
利用高效液相色谱分析技术对福建省茶园土壤中16种多环芳烃进行了定量分析,结果表明,PAHs的总量在0.622~812.0μg/kg之间,平均值为48.4μg/kg。其组成以3环的为主,4环次之,主成分分析和PAHs特征参数分析发现,福建省茶园土壤中多环芳烃主要以燃油、木柴和煤燃烧来源为主,部分样点存在油类排放污染。生态风险评价结果显示,福建省茶园土壤中多环芳烃已具有不利生物影响效应。  相似文献   

20.
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   

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