生活垃圾焚烧烟气排放中二噁英对人体健康的风险评价

随着垃圾焚烧的广泛应用,由此产生的二次污染问题也日益显现出来,特别是二嗯英污染已引起世界的关注。这也是垃圾焚烧设施在环评阶段遭到周围公众反对的原因之一。文中介绍了二嗯英的危害、垃圾焚烧烟气中的二嗯英来源以及二嗯英的相关标准。以某垃圾焚烧发电厂为例,对垃圾焚烧烟气中的二嗯英类物质对人体健康的风险进行了评价,并提出了如何最大限度地减少垃圾焚烧处理过程中的二唔英排放量。     

SCR装置对焦炉煤气燃烧废气中PCDD/Fs、PCBs和PCNs的协同脱除

研究了某大型焦化厂的选择性催化还原(SCR)装置对焦炉煤气燃烧废气中典型非故意产生持久性有机污染物(UPPOPs)的脱除效果,对SCR装置入口和出口废气和SCR装置降尘中二英(PCDD/Fs)、多氯联苯(PCBs)和多氯萘(PCNs)的全部异构体进行了分析.结果表明,SCR装置对总PCDD/Fs的脱除效率最高,为94.6%,对总PCBs和总PCNs的脱除率分别为74.7%和78.4%.SCR装置入口和出口废气中UP-POPs同系物的分布模式明显不同,入口处以高氯取代为主,出口处以低氯取代为主.SCR装置对高氯取代UP-POPs有更好的脱除效果.催化还原和催化氧化降解同时发生是SCR装置脱除废气中UP-POPs的重要机制.     

持久性有机污染物(POPs)对人类健康的危害及其治理技术进展

大部分持久有机污染物persistent organic pollutants(POPs)具有致癌性、致突变和致畸变作用，对人类健康造成严重危害。本文阐述了POPs的各种性质、对人类健康的危害、主要的污染来源、国内外面临的污染现状及其处理和销毁技术进展，着重阐述了对被POPs污染的土壤进行物理、化学和生物修复的技术，以及关于废气、污染土壤和水中二恶英类物质的治理技术。     

二英分子结构-水溶解度相关性密度泛函理论研究

运用密度泛函理论,在B3LYP/6-311G^**水平上,对多氯二苯并对二英(PCDDs)和多氯二苯并呋喃(PCDFs)的电子结构进行了优化,相应量子化学参数,即平均分子极化率(α)、熵(S)、极化率和四极矩的张量分量(α_xx、α_yy、α_zz和Q_xx、Q_yy、Q_zz)等用于该类化合物水溶解度的定量结构-性质相关性（QSPR）研究;基于内部误差一致的实验值,成功建立了3个QSPRs,其决定系数分别为0 .977、0 .968和0 .961;交叉验证相关系数分别为0 .968、0 .959和0 .946.模型分析表明,水溶解度主要与分子体积有关,而分子间相互作用的影响较小;不同QSPRs预测值间的差异可能与模型中预测变量本身性质和可获取实验值的有限性有关.与新近发展的QSPR相比较,本研究模型性能均有提高,这可能与B3LYP/6-311G^**精确计算电子性质和模型中引入四极矩张量分量有关.     

土壤中的二恶英类物质污染及其污染源

为加强对二恶英类物质污染现状及污染途径的调查研究,为切实有效地控制其污染,并为制定相关法律、法规提供可靠的依据,综合国外土壤中二恶英类物质环境污染调查的文献资料及本实验室对北京地区的调查研究结果,介绍了全球土壤的二恶英类物质污染概况,指出土壤中二恶英类物质的主要污染源有城市固体垃圾焚烧、有机含氯化合物的合成和使用、汽车尾气排放等,不同的污染源,其二恶英类物质特征分布形态不同,通过对样品中二恶英类物质的异构体类型及其分布形态的分析,可以追溯污染的起源。对北京地区的初步研究显示北京地区土壤中二恶英类物质的污染水平相对较低,但这还不足以说明该地区的二恶英类物质整体污染水平,还需对污染疑似地区土壤进行全面系统的研究,同时对全国其他地区的调查研究也是急为迫切的。     

持久性有机污染物的主要特征和研究进展

概述了持久性有机污染物(POPs)在环境中的主要存在类型、生态行为特征、污染效应和对环境生物体的健康危害特性及我国在该领域的主要研究进展.重点介绍了二NFDA7英类化合物的生态毒性表示法、主要处置技术与相关的检测方法等研究进展.我国POPs相关的基础研究相对滞后,要履行好POPs公约,还面临诸多需要解决的现实问题.当前开展适合我国国情的POPs物质的环境调查监测、环境安全与健康毒理学研究并建立相关的环境控制基准和评估体系十分必要.      

Fast extraction of polychlorinated dibenzo-p-dioxin and polychlorinated dibenzofuran in sewage sludge and soil samples

The current environmental legislations recommend monitoring chemical contaminants such as polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans before the use of sewage sludge on the agricultural land. In this study, a solid–liquid extraction with low-temperature purification (SLE-LTP) was optimized and validated to determine 2,3,7,8-tetrachlorodibenzo-p-dioxin and 2,3,7,8-tetrachlorodibenzofuran in sewage sludge and soil samples. The analyses were performed by gas chromatography-mass spectrometry operating in the selective ion mode (GC-MS-SIM). Acetonitrile:ethyl acetate 6.5:1.5 (v/v) was the best extraction phase, and the recoveries percentages were close to 100%. The linearity was demonstrated in the range of 1.25–25 µg L^?1 of 1.25–20 µg L^?1 for sewage sludge and soil, respectively. Matrix effect was proved for the two compounds and in the two matrices studied. Extraction percentages were between 78 and 109% and relative standard deviations ≤ 19%. The proposed method is faster than methods described in the literature because showed a few steps. The quantification limits (LOQ) in sewage sludge were 6.4 and 32 ng TEQ kg^?1 for 2,3,7,8-TCDF and 2,3,7,8-TCDD, respectively. In soil, LOQs were 0.8 and 8.0 ng TEQ kg^?1 for 2,3,7,8-TCDF and 2,3,7,8-TCDD, respectively. These values are lower than the maximum residue limits established by European Legislation. The method was applied to 22 agricultural soil samples from different Brazilian cities and 2,3,7,8-TCDF was detected in one of these samples.     

Characteristics of air pollution by polychlorinated dibenzo-p-dioxins and dibenzofurans in the typical industrial areas of Tangshan City, China

The ambient air in vicinity of different industrial sources for PCDD/PCDFs was sampled by TSP/PM10 active samplers and passive PUF disk samplers in Tangshan City, a metropolis containing clusters of various industrial plants. The TEQ concentrations of PCDD/PCDFs ranged from 44.2 to 394.1 fg I-TEQ/m3 with an average of 169.9 fg I-TEQ/m3. 2,3,4,7,8-PeCDF was the dominant contributor to PTEQ, contributing 41% (12% to 55%), while 1,2,3,4,6,7,8-HpCDF, OCDD and OCDF were the major congeners for the total concentrations. The ratios of PPCDF/PPCDD reached 2.54 on average, suggesting that de novo synthesis in thermal processes played an important role to the airborne pollution of PCDD/PCDFs. The similarities congener profiles indicated that TSP and PM10 active sampling methods are comparable for the determination of the PCDD/PCDFs in ambient air, and the ratios of concentrations determined by the two methods suggested that the PCDD/PCDFs tended to stay in fine particles. It was found that 2,3,7,8-TCDF and OCDD were the dominating congeners in the passive PUF disks samples. Through principal components analysis, the coke industry was suggested to be a relatively high potential emission source for PCDD/PCDFs in the ambient air of Tangshan, which was possibly formed by de novo synthesis mechanism. In this study, the atmospheric impacts to the environment from di erent industrial sources could be ranked as follows (from high to low): coking, iron sintering, steel making, power generation and chlorinate alkali chemical production industries.     

焚烧源二噁英的排放对周边土壤和植被污染的研究进展

经济的飞速发展和城市化进程的加快,带来了严重的生活垃圾负荷问题。垃圾焚烧技术因其具有减容化、无害化和资源化的优点,成为当今国际社会生活垃圾处理的主要技术之一。然而由于人们对于垃圾焚烧源可能产生的二噁英污染问题缺乏一个全面的认识,使得垃圾焚烧厂的建立遭到了民众的强烈反对,成为影响社会和谐稳定的因素;因此,需要对垃圾焚烧源二噁英的排放对周边土壤和植被的污染状况进行综述,对于解决老百姓对于垃圾焚烧二噁英污染的争议有巨大的现实意义。对近年来国内外学者在相关方面的研究进行了详细地综述,结果发现：国内已开展的研究仅限于二噁英对焚烧厂周边土壤的污染调查,而对于焚烧源二噁英对植被及农作物的污染的研究数据非常匮乏;而国外学者已开展的垃圾焚烧厂周边土壤和植被中二噁英污染的调查研究只是停留在二噁英在土壤和植被中总浓度的研究基础上,而对于不同二噁英同族物在焚烧厂附近土壤和植被中的分布特征和蓄积规律方面的研究比较缺乏,尤其是在其他污染源如废弃物的露天燃烧、交通等协同作用下,垃圾焚烧对二噁英污染贡献率的研究比较少,对于垃圾焚烧厂二噁英污染的控制没有起到直观的指导作用。本文指出今后的研究应加强对二噁英在焚烧厂周边土壤和植被中分布特征和蓄积规律研究,这对于焚烧源二噁英的污染防治以及对已被二噁英污染的土壤和植被的生态修复具有重要的意义。     

Emissions of PCDD and PCDF from combustion of forest fuels and sugarcane: a comparison between field measurements and simulations in a laboratory burn facility

Release of PCDD and PCDF from biomass combustion such as forest and agricultural crop fires has been nominated as an important source for these chemicals despite minimal characterisation. Available emission factors that have been experimentally determined in laboratory and field experiments vary by several orders of magnitude from <0.5 μg TEQ (t fuel consumed)⁻¹ to >100 μg TEQ (t fuel consumed)⁻¹. The aim of this study was to evaluate the effect of experimental methods on the emission factor.A portable field sampler was used to measure PCDD/PCDF emissions from forest fires and the same fuel when burnt over a brick hearth to eliminate potential soil effects. A laboratory burn facility was used to sample emissions from the same fuels. There was very good agreement in emission factors to air (EF_Air) for forest fuel (Duke Forest, NC) of 0.52 (range: 0.40-0.79), 0.59 (range: 0.18-1.2) and 0.75 (range: 0.27-1.2) μg TEQ_WHO2005 (t fuel consumed)⁻¹ for the in-field, over a brick hearth, and burn facility experiments, respectively. Similarly, experiments with sugarcane showed very good agreement with EF_Air of 1.1 (range: 0.40-2.2), 1.5 (range: 0.84-2.2) and 1.7 (range: 0.34-4.4) μg TEQ (t fuel consumed)⁻¹ for in-field, over a brick hearth, open field and burn facility experiments respectively. Field sampling and laboratory simulations were in good agreement, and no significant changes in emissions of PCDD/PCDF could be attributed to fuel storage and transport to laboratory test facilities.