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1.
水体悬浮颗粒物的扫描电镜与X射线能谱显微分析   总被引:3,自引:0,他引:3  
盛东  胡忻  刘锡尧 《岩矿测试》2010,29(6):683-686
通过对湖州地区74个土壤样品多环芳烃含量的测定,分析了湖州市不同土地利用类型土壤中多环芳烃(PAHs)的含量特征及污染水平。结果表明,湖州地区PAHs各组分的含量均有检出,各种土地利用类型表层土壤均受到一定程度的PAHs污染,但均小于荷兰土壤修复标准;湖州市区耕地中PAHs的含量最高;从PAHs低环/高环比值小于1以及芘/苯并(a)芘比值小于2,反映了湖州地区土壤中PAHs主要是由燃煤和生活污染产生的。  相似文献   

2.
太原市区土壤中多环芳烃污染特征研究   总被引:2,自引:0,他引:2  
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。  相似文献   

3.
<正>多环芳烃(PAHs)由于其持久性、生物富集效应和"三致"作用,对人类健康和生态环境构成极大威胁。其中,高环PAHs的高生物毒性和低生物可利用性使其具有高残留和高风险的特点,其环境行为和自然衰减逐渐成为当前研究热点。微生物降解是环境PAHs自然衰减的重要途径,也是PAHs污染土壤的主要修复手段。现阶段PAHs降解微生物的研究主要针对低环PAHs,依靠传统分离培养技术,其环境降解和代谢途径已相对清晰。但自然条件下PAHs的环境行为由于缺乏有效的技术  相似文献   

4.
《地下水》2021,(2)
以华北平原某多环芳烃类污染场地为例,选取苯并(a)芘为目标污染物,建立了污染场地地下水风险评估模型,采用局部敏感性分析方法研究EFO_a(成人室外暴露频率)、BW_a(成人平均体重)、DAIR_a(成人每日空气呼吸量)、AT_(ca)(致癌效应平均时间)、AT_(nc)(非致癌效应平均时间)以及土壤特征参数P_(ws)(土壤含水率)、ρ_s(土壤颗粒密度)、ρ_b(土壤容重)对地下水风险水平计算结果的影响。结果表明:8个参数对多环芳烃类污染场地地下水风险水平影响程度排序为ρ_b P_(ws)ρ_s AT_(ca)(AT_(nc)) EFO_a,其中没有影响的参数为BW_a和DAIR_a。  相似文献   

5.
近些年,随着我国城市化进程不断加快,土壤中多环芳烃污染已经成为威胁土壤环境质量和人体健康的主要因素。文章采集了北京市通州某改造区15件表层土壤(0~20 cm)样品,利用GC-MS分析技术,研究了土壤中美国环境保护署(USEPA)优控的16种多环芳烃(PAHs)的含量及组分特征,根据多环芳烃的空间分布特征和特定成分之间的浓度比值结合多元统计法分析了其污染来源,初步评价了其污染水平,并进行健康风险评价。结果表明:表层土壤中16种多环芳烃含量范围为6.57~8 307.2 μg/kg,均值为1 004.08 μg/kg。多环芳烃组分特征及Fla与(Fla+Pyr)、BaA与(BaA+Chr)的相对质量比值特征显示改造区是燃煤和汽车尾气混合型来源;多元统计后发现石油烃类污染源和化石燃料燃烧源是两种主要成分。最后参照《污染场地风险评估技术导则(HJ 25.3—2014)》对土壤中PAHs进行了健康风险评价,除苯并(a)芘(BaP)致癌风险值略偏高不可接受外,其余致癌与非致癌风险值均可接受。  相似文献   

6.
谢文泉  贾建亮  刘招君 《地质学报》2023,97(7):2363-2377
多环芳烃(PAHs)是古环境、古野火以及古气候的重要地质记录,本文通过气相色谱质谱法(GC- MS)研究了柴达木盆地北缘中侏罗统石门沟组煤中多环芳烃分布特征,检测出一系列二环至七环芳烃化合物,包括高等植物衍生多环芳烃(卡达烯、6- 异丙基- 1- 异己基- 2- 甲基萘、惹烯、西蒙内利烯以及二氢惹烯)和燃烧衍生多环芳烃(荧蒽、芘、苯并\[a\]蒽、、苯并荧蒽、苯并\[e\]芘、苯并\[a\]芘、茚并\[cd\]芘、苯并\[ghi\]苝和晕苯)等。这些多环芳烃的检出表明石门沟组煤沉积于具有显著陆源高等植物输入的微咸水湖沼环境,成熟度较低(平均随机反射率为056%)。石门沟组煤中高等植物衍生多环芳烃以极高的惹烯含量为特征,且存在较高丰度的西蒙内利烯和二氢惹烯,卡达烯丰度极低,反映出成煤期陆地植被类型以松柏类植物的针叶林为主,气候温暖湿润。同时,煤中丰富的燃烧衍生多环芳烃证实了柴达木盆地北缘中侏罗世存在广泛的陆地古野火,较高的大气氧气浓度(256%)可能是该时期野火频发的一个重要诱因。本次研究为柴达木盆地中侏罗世古野火事件的研究提供了重要的分子化石证据,也是对中侏罗世古环境和古气候研究的有益补充。  相似文献   

7.
<正>菲为一种典型的多环芳烃,具有"三致效应",在环境中分布广泛。当前利用微生物将多环芳烃转化成为无害物质的生物修复技术受到广泛关注(Samanta,2002)。目前有关环境因素对土壤中菲降解影响的研究,主要关注水分、养分、土壤物理条件等,对天然矿物的影响关注较  相似文献   

8.
长期以来,研究者在探讨土壤中多环芳烃(PAHs)的降解及修复过程中,缺乏简便有效的手段对化合物的降解动态进行定量研究。前人尝试用投加实验、对比采用降解措施前后污染物的浓度变化、模型计算等方法研究PAHs的降解过程,其结果常互相矛盾,或不能真实反映复杂的实际环境。本文应用单体碳同位素技术对农田土壤中多环芳烃的植物降解过程进行定量表征,采集了某地农田表土作为供试土壤,选择玉米作为供试作物,开展了作物对土壤中PAHs降解及消除过程的研究。气相色谱-质谱分析结果表明,培养所用的玉米原始土及分4批收集的空白土、根际土、非根际土样品中16种PAHs的浓度总和(∑PAHs)平均分别为380.8 ng/g、(281.5±34.7) ng/g、(272.2±11.6) ng/g和(299.8±37.9) ng/g;玉米生长期间,各土壤样品 的∑PAHs均比原始土壤有所下降,但除3环化合物(苊烯、苊、芴、菲、蒽)外,其他化合物并未随玉米的生长表现出显著趋势。与玉米根、叶倾向于富集低环PAHs化合物相对应,可以判断植物对土壤中的低环化合物去除作用最为显著。各采样时期玉米根际土、非根际土和空白土壤样品中多环芳烃单体化合物的碳同位素分馏值(δ13C)在-34.31‰~-23.95‰之间,且除芘外的其他化合物的δ13C值随时间呈现逐步变轻的趋势,波动值位于-0.6‰~-9.0‰之间;本文对于PAHs单体化合物,尤其是4、5环化合物,在玉米降解过程中的碳同位素分馏与浓度变化之间未发现明显关系。考虑3环以下的PAHs化合物更倾向于被降解和清除,且其碳、氢同位素分馏情况更容易被观察到,因此稳定同位素分析更有助于探明该类单体多环芳烃污染物在环境中的迁移、转化规律。  相似文献   

9.
张士灌区细河流域地下水及土壤中有机污染严重,其中多环芳烃菲超标。从研究区污染土壤中取土著微生物,控制实验条件与研究区潜水环境一致,通过实验室选择性富集培养分离出20株以菲为唯一碳源和能源的细菌。经降解实验,在温度为10℃、pH值为7.5的环境条件下筛选出1株在9天内对菲(50mg/L)的降解率达到85%以上的菌株BC。该菌株在温度为5~30℃,pH为6.0~9.0条件下15天内对菲的降解率可达到96%以上。研究结果为张士污灌区及相似地区地下水和土壤环境中菲的原位生物降解法的应用提供了技术依据。  相似文献   

10.
以我国东部某城市城区表层土壤环境指标为研究对象,采用一元线性回归和主成分分析的方法研究了城市土壤中六六六(HCHs)、滴滴涕(DDTs)、多环芳烃(PAHs)、有机质含量,含水量,重金属含量,土壤pH值等指标间的相关性,确认长期的工业活动是导致土壤重金属和多环芳烃污染的主要来源,城市绿地施用农药是土壤六六六和滴滴涕污染的主要来源。  相似文献   

11.
菌根真菌对土壤中有机污染物的修复研究   总被引:12,自引:0,他引:12  
菌根真菌是真菌与植物之间特殊的联合共生体,利用菌根真菌修复土壤,尤其是修复有机污染物污染的土壤,正成为一个崭新的研究方向。菌根真菌是土壤真菌的一种,但与土壤中放线菌和细菌等微生物相比,其对土壤中有机污染物具有更大的忍耐能力,并且能利用土壤中大多数持久性有机污染物作为碳源来获取能量。综述了近20年菌根真菌对土壤有机污染物降解研究,讨论了菌根真菌降解土壤有机污染物的可能机制,并探讨了从引入固氮菌、外源细菌两个方面对菌根调控以提高修复效果的可能性,为进一步研究菌根真菌生物降解土壤中持久性有机污染物、利用菌根植物修复有机污染土壤提供信息。  相似文献   

12.
表层岩溶带土壤中多环芳烃分布特征及来源解析   总被引:3,自引:0,他引:3  
利用气相色谱-质谱联用仪(GC-MS)对表层岩溶泉域土壤中的16种优控的多环芳烃(Polycyclic Aromatic Hydrocarbons, PAHs)含量进行了分析,并对其组成、污染水平和来源进行了探讨。结果表明,16种优控PAHs在表层岩溶泉域土壤中的检出率为100%,其含量介于439.19~3329.72ng/g之间,平均值为1392.44ng/g,7种致癌性PAHs占总量的26%。PAHs的组成特征受地形的控制,随着海拔升高,低环PAHs所占比例升高,高环PAHs比例降低。同分异构体比值分析表明,研究区土壤中的PAHs主要来自于煤、生物质和石油的燃烧排放。研究区土壤中16种PAHs的TEQcarc值介于18.65~501.13ng/g,平均值为140.57ng/g。7种致癌性PAHs占总TEQcarc的比例达到96.8%。研究区表土中,后沟泉域的污染程度最大,次之是兰花沟泉域和柏树湾泉域,水房泉泉域的污染程度最小,但由于柏树湾泉域松针落叶中BaP、PAHs含量较高,松针落叶中PAHs含量分别高达36.36ng/g和2370.1ng/g,土壤生态风险评价中应考虑松针落叶层的潜在影响。   相似文献   

13.
《Organic Geochemistry》1999,30(8):891-900
The fate of polycyclic aromatic hydrocarbon (PAH) mixtures in marine sediments can be difficult to determine due to extraction, analytical and matrix barriers. The purpose of this work was to develop and validate methods to kill indigenous microorganisms in marine sediments, to spike the sediments with a mixture of PAHs in a minimally invasive fashion and to age the treated sediments while following the effects of the treatments on the PAHs and several groups of microorganisms. Following gamma irradiation (0.0, 2.5, 3.5 and 5.0 Mrad), the sediments were mixed with known amounts of PAHs that had been coated onto fine-grained sand. During the subsequent ageing process, levels of extractable PAHs and numbers of microorganisms were monitored. The addition of PAHs to the unirradiated sediment seemed to rapidly induce the degradation of phenanthrene, fluoranthene and pyrene, while these PAHs decreased to a much smaller extent in the irradiated sediments in the 376 days of the experiment. The heavier PAHs, chrysene and benzo(a)pyrene, showed slight decreases in extractable concentrations at all irradiation levels, suggesting PAH sequestration/ageing over time. While some microbial populations recovered rapidly, culturable PAH degraders did not recover at any irradiation level tested and concentrations of light molecular weight PAHs in sediments irradiated at all levels dropped only slightly. This suggests that even the lowest dose (2.5 Mrad) may inhibit PAH degradation sufficiently to permit ageing of the spiked sediments for 6 months to a year. The methods described show promise for the generation of realistic, well-characterized spiked sediments for use in biodegradation and bioavailability experiments.  相似文献   

14.
Soil contaminated sites contain a variety of pollutants, especially heavy metals and polycyclic aromatic hydrocarbons (PAHs). Interactions between heavy metals have been relatively well studied, but little is known about interactions between heavy metals and PAHs. The combined effect of heavy metals and PAHs on soil microorganism was studied in laboratory conditions and evaluated by random denaturing gradient gel electrophoresis. We extracted DNA directly from contaminated soils and then amplified the V3 sequences of the 16S rDNA. The results showed that with different culture time, the gene diversity of the single and combined contaminated soil differed as well. After 15 days of culture, the microorganisms were stimulated and accommodated. After 45 days of cultivation, the quantities of the soil microorganisms were affected. It is concluded that some of the microorganisms utilize phenanthrene as important carbon resources. Microorganisms directly isolated from soil could reflect the diversity of soil microorganism and population distribution conditions.  相似文献   

15.
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, BCCr) and chemo-thermal oxidation (CTO-375, BCCTO). 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 BCCr concentration (4.65 g/kg on average) was significantly higher than BCCTO (1.91 g/kg on average) in Shanghai soils. BCCr concentrations in industrial area were significantly higher than those in other two. Stronger correlation was found between PAHs and TOC, BCCr than that between PAHs and BCCTO, 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.  相似文献   

16.
The analysis of PAHs (polycyclic aromatic hydrocarbons) in karst environments has provided an assessment of the vulnerability of karst water and the study of PAH records in stalagmites. The major source of PAHs has generally been considered to be the soil. In this study, we report the quantification of PAHs in the ecosystem compartments of a mountain karst system over a snow-melting period and the spring to summer dry period. PAH profiles in karst seepage waters were consistently similar to those in wet deposits, following the change in PAH profiles between winter and summer periods. However, PAH signatures of atmospheric wet deposits were modulated by a loss of the high molecular weight PAHs, which appear to accumulate in soils. A PAH mass balance was calculated during a summer storm event. This mass balance suggests that dry deposits and canopy throughfall could account for the PAH abundance in karst seepage waters. This study demonstrates the ability of organic hydrophobic compounds to be directly transferred from the atmosphere or canopy into seepage waters, giving new emphasis to the study of PAHs recorded in stalagmites.  相似文献   

17.
《Organic Geochemistry》1999,30(8):937-945
The anaerobic degradation of the polycyclic aromatic hydrocarbons (PAHs) naphthalene and phenanthrene was investigated in several marine harbor sediments. In sediments from Boston Harbor that were heavily contaminated with petroleum, [14C]-naphthalene and [14C]-phenanthrene were oxidized to 14CO2 without a lag, suggesting that the microbial community was adapted for anaerobic PAH oxidation in situ. The addition of molybdate, a specific inhibitor of sulfate-reducing microorganisms, inhibited PAH mineralization which suggested that sulfate reducers were involved in the anaerobic oxidation of the PAHs. PAHs were also anaerobically oxidized at another site in Boston Harbor that was less heavily contaminated, but at a slower rate than in the most heavily contaminated sediments. Sediments not contaminated with petroleum did not significantly oxidize the PAHs. A similar correspondence between rates of anaerobic PAH oxidation and the degree of PAH contamination was observed in sediments from Tampa Bay and San Diego Bay. When relatively pristine sediments from San Diego Bay that did not have a significant capacity for anaerobic PAH oxidation were exposed to high concentrations of naphthalene, they developed a potential for naphthalene degradation that was comparable to that in sediments that had a history of PAH contamination. The increase in potential for naphthalene degradation in the sediments exposed to naphthalene was associated with an increase in naphthalene-degrading microorganisms. These results suggest that many marine harbor sediments contain microorganisms capable of anaerobically oxidizing PAHs under sulfate-reducing conditions and that these microorganisms will respond with an increase in their activity when PAHs are introduced into the sediments. Thus, if PAH inputs into harbor sediments from petroleum can be reduced there may be a widespread potential for microorganisms to remove this PAH contamination from the sediments, despite anaerobic conditions.  相似文献   

18.
This study aims to explore the condensation and fractionation trends of persistent organic pollutants (POPs) in the karst soils. The tiankeng is a karst surface expression that can act as a focal point for introduction of contaminants to a karst aquifer, which may serve both as condenser for vapor phase POPs and as barrier/sink for particulate associated less volatile POPs. The fractionation of POPs in soils from the upper rim and floor of tiankeng is of interest in understanding the role of tiankeng in the long-distance transport of POPs. In the present study, polycyclic aromatic hydrocarbons (PAHs) in the surface soils from the upper rim and floor of Dashiwei tiankeng in Southern China were analyzed. The total PAH concentrations in soils were 23.40–190 ng g−1, with phenanthrene being the most abundant. The distribution patterns of PAH compounds in the soil samples matched well with their properties. It indicated the heavy PAHs were susceptible to retention by the floor soils of tiankeng than light PAHs. A plot of Cfloor/Crim against PAH molecular weight gave a good positive relationship in the molecular weight range of 152–276. It is suggested that the floor soils can be focal points of more concentrated PAH and deserve attention. The concentrations of total PAHs in the floor soils (43.40–190 ng g−1, mean 87.76 ng g−1) were higher than those in the upper rim (23.40–88.94 ng g−1, mean 57.74 ng g−1). In addition, there was a shift in compound pattern with an increase in the proportion of light PAHs (2–3 rings), a decrease in heavy PAHs (5–6 rings) and a relatively stable content of 4-ring PAHs. A combination of particulate scavenging and cold condensation is proposed as the major mechanism for the compositional fractionation of PAHs in the soils from the upper rim and floor of tiankeng.  相似文献   

19.
On the basis of site investigation and sample collection of petroleum contaminants in the soil-water-crop system in the Shenyang-Fushun sewage irrigation area, the physical-chemical-biological compositions of the unsaturated zone is analyzed systematically in this paper. At the same time, the degradation kinetics of residual and aqueous oils is determined through biodegradation tests. The studies show that dominant microorganisms have been formed in the soils after long-term sewage irrigation. The microorganisms mainly include bacteria, and a few of fungus and actinomycetes.After a 110-days‘ biodegradation test, the degradation rate of residual oil is 9.74%--10.63%, while the degradation rate of aqueous oil reaches 62.43 %. This indicates that the degradation rate of low-carbon aqueous oil is higher than that of highcarbon residual oil. In addition, although microbial degradation of petroleum contaminants in soils is suitable to the firstorder kinetics equation, the half-lives of aqueous oil, No. 20 heavy diesel and residual oil in the surface soils (L2-1, S1-1 and X1-1) are 1732 h, 3465 h and 17325 h, respectively.  相似文献   

20.
The polycyclic aromatic hydrocarbon (PAH) contamination of urban, agricultural and forest soil samples was investigated from samples obtained in the surroundings of Valasske Mezirici. Valasske Mezirici is a town located in the north-east mountainous part of the Czech Republic, where a coal tar refinery is situated. 16 PAHs listed in the US EPA were investigated. Organic oxidizable carbon was also observed in the forest soils. The PAH concentrations ranged from 0.86-10.84 (with one anomalous value of 35.14) and 7.66-79.39 mg/kg dm in the urban/agricultural and forest soils, respectively. While the PAH levels in the urban/agricultural soils are within the range typically found in industrialized areas, the forest soils showed elevated PAH concentrations compared to other forest soils in Western and Northern Europe. The PAH concentrations and their molecular distribution ratios were studied as functions of the sample location and the meteorological history. The soils from localities at higher altitudes above sea level have the highest PAH concentrations, and the PAH concentrations decrease with increasing distance from the town.  相似文献   

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