垃圾焚烧厂恶臭污染物分布特征及健康风险评价

以北京某典型垃圾焚烧厂为研究对象,分析了其不同工艺流程中的恶臭污染物浓度,并进行了健康风险评价。结果表明:(1)共有60种恶臭污染物检出,不同工艺流程中的恶臭污染物总质量浓度由大到小依次是垃圾料坑((128.20±3.63)mg/m3)渗滤液池((58.50±3.45)mg/m3)卸料区((45.70±1.34)mg/m3)炉渣堆放处((22.63±1.38)mg/m3)烟气净化系统((9.33±0.88)mg/m3)。(2)有13种恶臭污染物阈稀释倍数大于5,其在不同工艺流程中的理论臭气浓度排列顺序与恶臭污染物总浓度一致。(3)卸料区和渗滤液池的非致癌风险危害指数大于1,可能存在非致癌风险,主要非致癌风险物是苯和二甲苯。卸料区、炉渣堆放处和渗滤液池的终生致癌风险大于10-4,存在较大致癌风险,主要致癌风险物是苯和乙苯。建议该垃圾焚烧厂加强对恶臭污染的控制和处理,做好对职业暴露人群的健康防护。     

江苏省城市垃圾焚烧电厂烟气中重金属排放研究

通过对江苏省现有垃圾焚烧电厂进行资料统计,分析了江苏省目前垃圾焚烧电厂规模及分布情况。选择典型垃圾焚烧电厂烟气进行现场采样监测,对垃圾焚烧电厂烟气中重金属铅、汞、镉含量进行分析。根据垃圾焚烧电厂相关信息,结合烟气中重金属含量及相关参数,估算江苏省垃圾焚烧电厂3种重金属年排放量,其中铅为2 010.50kg/a,汞为9.16kg/a,镉为424.63kg/a。根据垃圾焚烧电厂区域分布状况,引入地学模型,对垃圾焚烧电厂重金属区域分布特征进行了分析,结果显示江苏省东部明显高于西部,苏南高于苏北地区,其中苏南地区重金属排放量最大,铅、汞、镉分别占到垃圾焚烧排放总量的48%、51%、60%。通过重金属地学分析和数据统计,确定了江苏省垃圾焚烧重金属排放重点防控区域为苏南地区。     

国内外生活垃圾焚烧烟气排放与监管标准比较分析

我国生活垃圾焚烧发电规模占全球的66.1%,环境风险不容忽视,需要制定适宜的烟气污染物排放限值与监管措施,可参考欧盟、美国、日本等较早应用生活垃圾焚烧处理的国家 (地区) 的有益经验。但是,现有的国内外对比研究仅关注了排放限值的差异,忽略了国内外标准在历史沿革、基准条件、适用对象、执行尺度等方面的差异及原因。本研究基于2017年以来国内生活垃圾焚烧行业专项整治取得的成效,深入分析国内外标准的差异及原因,得出以下结论：1) 烟气排放限值落地执行需要与之配套的监管措施,自动监测手段有利于实现对生活垃圾焚烧烟气常规污染物及炉温的全天候监管,在欧盟、美国已广泛应用,在我国的应用已取得良好成效;2) 与国外相比,我国生活垃圾焚烧烟气排放限值未考虑焚烧炉规模与技术差异化的影响,在排放与监管标准中未兼顾小型焚烧炉,但实际上有必要给予小型焚烧炉适度的、合理的差异化要求,以规范市场并增强环境监管的严肃性;3) 与国外相比,我国生活垃圾焚烧烟气排放限值总体上处于严格行列,监管刚性很强但柔性不足,部分省市制定的地方标准限值严于欧盟,但缺乏类似欧盟标准B类限值的达标评价方式,有必要在探索“正面清单”等更为灵活的监管方式的同时,基于自动监测手段表现出的精准监管能力,进一步优化和拓展更具弹性的排放限值与监管措施。本研究有利于识别我国生活垃圾焚烧行业环境监管政策和模式与发达国家 (地区) 的差异,可为进一步优化固定源环境监管政策和模式提供依据。     

危险废物事故排放的河流水环境健康风险评价

分析了基于水体中污染物迁移转化方程的水质预测模型,并借鉴美国环保局推荐使用的健康风险评价模型,建立了一种危险废物事故排放时水环境对人体健康风险的评价方法。以电镀污泥为例验证了该方法的有效性。结果显示:该方法需要参数少且计算简单;电镀污泥中目标污染物(Cr、Cu、Ni、Zn)所引起的河流水环境非致癌风险(1.67)超过了美国标准中的可接受风险水平1.00,不可接受;致癌风险(0.88E-11)则小于美国标准中的可接受风险水平1.00E-06,风险不明显。     

海浪河水环境重金属污染健康风险评价

为阐明海浪河地表水体中重金属污染物的分布特征与风险水平,对研究区域内As、Cd、Zn、Cu、Pb、Mn等重金属污染物浓度进行了分析检测,并采用美国环境保护局(USEPA)推荐的健康风险评价模型对水体中重金属引起的健康风险进行了评价。结果表明,各采样点的重金属监测数据中As、Cd、Zn 和Cu均达到Ⅱ类水质标准,符合水环境功能区划要求,Pb是海浪河主要超标污染物。海浪河重金属As和Cd的健康风险值远远大于Zn、Cu、Pb和Mn的健康风险值,风险值相差4~5个数量级。致癌物As的健康风险值最大,在S5和S6采样点分别达到了5.81×10-5和9.43×10-5a-1,均高于最大可接受风险水平5.0×10-5a-1。     

城市自来水中挥发性有机氯污染物检测及健康风险评价初步研究

水质安全是饮用水安全的重中之重,直接关系到人体健康。采用健康风险评价模式,对某市饮用水进行了分析和评价。研究结果表明,该市通过饮水途径引起的非致癌健康风险中四氯化碳最大,三氯甲烷次之,两者风险水平在10-5～10-6,远低于美国环境保护署推荐的最大可接受风险水平。通过饮水途径所致健康风险中,四氯乙烯所引起的致癌风险最大(1.2×10-8),但远远低于美国环境保护署推荐的通过饮水途径最大可接受风险水平(5×10-5)。根据美国环境保护署的推荐值,初步认为目前该市饮用水中挥发性有机污染物不会对人体产生明显的健康危害。     

污水再生利用的健康风险评价方法

随着经济发展和人口增加，中国水资源短缺问题日益严重，水资源再生利用成为解决中国水危机的重要途径。再生水对人体健康的风险成为人们关注的焦点。应用风险评价技术评估再生水的健康风险目前再生水回用迫切需要解决的问题，作者论述了再生水风险评价的基本理论和评价方法及存在的问题。     

江苏某市水稻籽粒重金属富集特征及健康风险评价

为评估食用重金属污染土壤所产水稻对人体健康产生的风险,选取江苏省某市16个乡镇393组水稻籽粒-根际土为研究对象,考察As、Cd、Cr、Hg、Pb的质量浓度和富集特征;利用单因子污染指数法分析水稻籽粒的重金属污染特征,并用健康风险指数(HQ)评估重金属对人体健康的潜在风险.结果表明:Cd的富集系数远高于其他重金属,说明...     

南方某典型矿冶污染场地健康风险评价及修复建议

矿区及周边土壤重金属污染不容忽视,砷、镉和铅等对周边人群造成较高的健康风险隐患。以南方红壤区某铅锌冶炼矿区污染场地为研究对象,开展危害识别、暴露评估、毒性评估及风险表征,并讨论场地修复目标值与修复技术。结果表明：土壤受到重金属复合污染,关注污染物为四类重金属,包括铅、砷、镉和锌,集中于表层土壤（0~0.6 m）,并呈现空间分布规律性;场地未来用地类型为工业用地,对比污染物（不包括铅）各层（第1层0~0.3 m、第2层0.3~0.6 m、第3层0.6~1.0 m）风险表征值,污染物（砷、镉）存在致癌风险与非致癌危害,研究区重金属污染累积风险水平不可接受;分析风险控制值及国内外相关标准限值等,初步建议砷、镉和铅的修复目标值分别为13.41、21.50和600 mg·kg-1;同时,针对场地污染现状及健康风险,建议源控制与修复技术并用,并与当地工业园区建设统筹开展。     

三峡水库135 m蓄水前后水体重金属环境健康风险评价

三峡水库135 m蓄水后,水体中各重金属的单因子污染指数和Nemerow综合污染指数均有不同程度的增大,特别是Pb污染应该引起重视.健康风险评价结果表明,成库前后非致癌有毒化学物质(Hg、Pb和Cu)所引起的健康危害的个人年风险为Pb＞Cu＞Hg,致癌物质对人体健康危害的个人年风险均大于非致癌物.各类污染物所致个人平均健康危害成库前后均低于国际辐射防护委员会(ICRP)推荐的标准,为可接受水平.     

Dehalogenation Potential of Municipal Waste Incineration Fly Ash

BACKGROUND, AIMS AND SCOPE: In the first part of this paper the main principles which control the dehalogenation of polychlorinated aromatic compounds on municipal waste incineration fly ash (MWI-FA) have been discussed and the model fly ash of similar dehalogenation activity has been proposed. Even if both systems show comparable dehalogenation properties, the main question concerning the postulated identical reaction mechanism in both cases is left unanswered. The other very important point is to what extent is this dechlorination mechanism thermodynamically controlled. The same problem is often discussed in the literature also for the de novo synthetic reactions. From the data it is clear that metallic copper plays a decisive role in the mechanism of the dehalogenation reaction. Although the results reported in the first part strongly support the idea that copper acts in this dechlorination as the reaction component, in contrast to its generally accepted catalytic behaviour, we believed that additional support for this conclusion can be obtained with the help of a thermodynamic interpretation of the mechanism of the reaction. RESULTS AND DISCUSSION: The pathways of hexachlorobenzene dechlorination on MWI-FA and model fly ash were studied in a closed system at 260-300 degrees C under nitrogen atmosphere. These pathways were the same for both systems, with the following prevailing sequences: hexachlorobenzene --> pentachlorobenzene --> 1,2,3,5-tetrachlorobenzene --> 1,3,5-trichlorobenzene --> 1,3-dichlorobenzene. Thermodynamic calculations were carried out by using the method of minimization total Gibbs energy of the whole system. In the calculations, the following reaction components were taken into account: all gaseous chlorinated benzenes, benzene, hydrogen chloride, a gaseous trimer Cu3Cl3, and also Cu2O and CuCl2 as solid components. The effect of the reaction temperature and the amount of copper and water vapour were considered as well. The effect of reaction temperature was determined from the data calculated for the 500 to 750 K temperature region. The effect of the initial composition was determined for the molar amounts of copper = 0.01-3 moles and water vapour = 0.2 to 3 moles per mole of chlorobenzene isomer CONCLUSIONS: The results of hexachlorobenzene dechlorination by MWI-FA and model fly ash under comparable reaction conditions allow us to conclude that both dechlorinations proceed via the same dechlorination pathways, which can be taken as an evidence of the identical dehalogenation mechanism for both systems. The relative percentual distribution of the dehalogenated products depends on the temperature, but not on the initial amount of water vapour or copper metal. On the other hand, the initial amount of copper substantially affects the conversion of the dehalogenation as well as the molar ratio of Cu3Cl3 to HCl in the equilibrium mixture. Comparison of the experimental with thermodynamic results supports the idea that dehalogenation reactions are thermodynamically controlled. RECOMMENDATIONS AND OUTLOOK: Thermodynamic analysis of the dehalogenation reactions may prove useful for a wide range of pollutants. The calculations concerning polychlorinated biphenyls and phenols are under study.     

Assessment of Human and Ecosystem Risk Due to Agricultural Waste Compost Application on Soils: A Review

Agricultural wastes (AW) are often characterized by varying pH and substantial contamination potential, which are mainly related to their high organic load, thus affecting—when improperly disposed of—soils, living organisms, and water bodies. Composting of AW is the most commonly used management option and results in the production of soil improver that enhances crop growth and contributes to agricultural sustainability. This study aims to present the framework for assessing human and ecosystem risk when compost produced from AW is applied on soil. In order to develop this framework, issues such as origin, composition and pre-treatment of AW, application rates on soils, bioavailability and mobility of contaminants present in compost, exposure routes and rates as well as determination of the fate of contaminants in soil, air, and water, should be taken into consideration.     

基于k-Means算法的生活垃圾焚烧设施烟气二恶英防控

为深入探究生活垃圾焚烧设施二恶英的防控方法,采用k-Means算法对华南某生活垃圾焚烧发电厂焚烧设施的运行状态和不同炉内状态下二恶英排放特征及控制机理进行研究。结果表明,该厂3台焚烧炉具有显著不同的运行状态 (类别1和2) (p<0.05) ,在不同状态下,其常规污染物及二恶英排放特征差异显著 (p<0.05) ,类别1炉内状态较差,其排放的CO质量浓度是类别2状态下的2倍,二恶英的质量浓度是类别2状态下的1.5倍。类别1和类别2状态下二恶英的主导生成机理分别为“前驱物合成反应”和“从头合成反应”。为降低二恶英的排放,该厂首先应保证烟气流量大于10.5×10⁴ m³·h⁻¹ (均值11.8×10⁴ m³·h⁻¹) ,其余参数最优范围为：烟气含氧量大于7.0% (均值8.6%) 、CO质量浓度低于9.0 mg·m⁻³ (均值3.5 mg·m^-3) 、烟气湿度小于23.7% (均值21.3%) 、烟气温度为140~154 ℃ (均值145.7 ℃) 。当通过运行控制手段无法保持上述参数控制范围时,应分析原因并考虑停炉检修。本研究结果可为优化焚烧过程、降低二恶英排放、生活垃圾焚烧发电厂长期稳定运行的判别和精细化管理提供参考。     

焦化行业的环境风险评价方法

结合具体实例，对焦化行业环境风险评价中，环境风险污染源的识别、影响预测及环境风险的减缓措施和应急预案的制定等评价方法进行了分析。     

固定源废气监测工作的若干问题探讨

从监测工况、测点位置、采样过程、结果计算等方面,结合实际经验,对大气固定污染源的监测工作中存在的一些疑难问题进行了探讨。     

Spatio-Temporal Distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in Atmospheric Air of Tamil Nadu,India, and Human Health Risk Assessment

This study analyzed the seasonal distribution and the possible sources of polycyclic aromatic hydrocarbons (PAHs) in the atmospheric environment of Tamil Nadu, India. Passive air sampling was performed at 32 locations during the period from April 2009 to January 2010, and PAHs were quantified using a gas chromatograph-mass spectrometer. Analysis showed that the concentrations of PAHs were in the range of 5–47.5 ng/m³ with uniform distribution in urban areas in all seasons. Pre-monsoon season showed the highest cumulative concentration of PAHs in both agricultural and coastal areas. Among PAHs, phenanthrene, fluoranthene, and pyrene levels were found to be predominant in all the samples, contributing up to 36%, 35.5%, and 24.5% of total PAHs, respectively. The signature of the PAHs obtained through diagnostic ratio and principal component analysis revealed that diesel emissions was the probable source of PAHs in all locations. Based on Word Health Organization guidelines, the human lung cancer risk due to observed level of PAH concentration (i.e., PAHs exposure) is meager. However, the risk is predicted to be more in the coastal area during summer (18 individuals among 0.1 million people). To the knowledge of these authors, this report is the first on the seasonal analysis of PAHs using passive air sampling in India.     

Assessment of daily intake of organochlorine pesticides from milk in different regions of Poland

The common occurrence of organochlorine compounds in the environment, food and human tissues may constitute a serious threat to human health. The method of gas chromatography-mass spectroscopy was used to determine the content of pesticides in 15 samples of raw cow's milk from different regions of Poland. The results revealed high levels of p,p′-DDE, p,p′-DDT, heptachlor and aldrin. The studied milk contained lindane in average concentrations within the maximum limits. Although in 20% of all samples tested, the concentration of lindane exceeded permissible limits, while in 15% of samples the content of Σ DDT was too high. But the average daily consumption of milk containing organochlorine pesticides poses no direct threat to human health, because daily intake (DI) for all compounds were below the acceptable daily intake (ADI). Attention should be paid to the exposure of consumers to pesticide residues from other dairy foods.