贵州东部某燃煤电厂汞排放对周边环境空气及土壤的影响

结合当地气象条件,测定贵州省东部某燃煤电厂下风向环境空气汞浓度分布情况,同时测定该燃煤电厂周边表层土壤中汞含量,并对其污染程度进行评价,探讨了土壤汞与理化性质间的相关性。结果表明,该燃煤电厂下风向环境空气汞浓度远高于北半球大气气态总汞背景值,空气汞浓度在2.7 km范围内随距离的增大而增大,在2.7~5.0 km范围内汞浓度随距离的增大而减小。电厂周边表层土壤汞含量是贵州省A层土壤Hg背景值的8.5倍,存在中度到重度程度的污染,土壤Hg与土壤pH呈正相关性,但与土壤有机质未表现出相关性。     

东北地区大气BTEX的时空分布特征

在东北地区7个典型城市中25个监测点进行了观测,时间分别为2008年4月、7月、10月和2009年1月,使用吸附剂采样管采集并通过热脱附-气相色谱-质谱联用技术分析了苯系物样品,系统研究了东北地区大气苯系物的时空分布特征。研究结果表明,苯和甲苯年均浓度值最高,分别为(4.19±2.31)μg/m3和(3.22±1.14)μg/m3,共占苯系物浓度近70%;各功能区按苯系物浓度大小顺序排列为混合区工业区交通区居民区文教区对照区;受排放源和气象条件的影响,采暖期苯系物浓度高于非采暖期苯系物浓度;风向频率影响苯系物浓度分布,沿下风向浓度逐渐降低;苯/甲苯比值分析表明,东北地区苯系物的主要来源是煤燃烧。     

新疆某焦化厂硫化氢、二氧化氮与苯系物的检测与分析

通过对某焦化厂生产过程环境空气中,可能含有的影响职工身体健康的危害因素开展了职业卫生调查,提出合理的可预防措施和建议。利用定点采样和个体采样相结合的方法对该焦化厂一期练焦生产作业环境周围及行政办公楼周边空气进行每月连续检测7 d,为期11个月的检测与分析。参照相关的职业卫生标准和规范,针对该焦化厂一期生产作业环境空气中存在的潜在有害因素种类及各项浓度及强度,进行综合分析和评价。现场检测结果表明:炼焦评价单元、行政办公楼、测温区所设定检测点的硫化氢、二氧化氮、苯、甲苯、二甲苯浓度均低于我国职业卫生规定的长时间接触允许浓度的十分之一,合格率为100%,所处的风险等级为1。此工作区域空气中所含有的有毒、有害的化学物质对人体健康带来的风险可以忽略不计。     

“3．29”液氯外泄污染事故的环境调查

对京沪高速公路淮安段上行线103K＋30M处发生一起交通事故，造成液氯泄漏事故进行了调查．结果表明，这次液氯泄漏事故对周围的环境空气造成了严重的污染，散布于空气中的氯气，给附近的居民造成巨大的伤亡，还有大量的禽畜死亡．文章提出了建立健全突发性污染事故的应急处理系统；完善相关的法律、法规；加强区域管理．     

乌鲁木齐土壤中多环芳烃的污染特征及生态风险评价

在乌鲁木齐地区不同功能区采集28个表层土壤样品,对土壤中多环芳烃(PAHs)的污染特征进行研究,并运用正定矩阵因子分析法对其来源进行分析,采用苯并[a]芘的毒性当量浓度(TEQBa P)对PAHs的生态风险进行评价。研究显示,土壤中∑16 PAHs含量为331~15 799μg/kg,其平均值为(5 018±4 896)μg/kg(n=28),以3环、4环为主。∑16PAHs的浓度呈现出交通区工业区公园区农业区居民商业区的变化趋势;正定矩阵因子分析法表明,乌鲁木齐表层土壤中PAHs的主要来源及贡献分别为煤的燃烧(51.19%),汽油车燃烧(19.02%),柴油车燃烧(18.35%),机动车石油的泄漏(11.42%);53%的采样点TEQBa P值超过荷兰土壤标准目标参考值,主要集中在交通区和工业区。     

云南省宣威市和富源县空气和土壤中多环芳烃污染水平研究

宣威市和富源县位于我国云南省东北部,是全世界肺癌发病率最高的地区之一。当地居民在不通风的房间内燃烧烟煤做饭或取暖造成了严重的室内空气污染。研究表明,长期暴露在燃煤造成的污染物中是导致两地居民肺癌持续高发的主要原因,多环芳烃是最可疑的致病因子之一。2008年1月,分别用聚胺脂泡沫和玻璃纤维滤膜采集了当地9个点位室内、室外空气中气相和颗粒物相中的多环芳烃,同时采集了对应点位的土壤样品。通过对样品的分析,考察了当地空气和土壤中多环芳烃的污染水平、特征以及来源。结果证明,当地空气和土壤中存在严重的多环芳烃污染,室内污染显著高于室外,然而随着当地工业的发展室外污染同样不可忽视,主成分分析结合比值法证明,当地室内外多环芳烃的主要污染源来自于煤炭的燃烧。对空气颗粒物和土壤中多环芳烃浓度进行了比较,对土壤中多环芳烃的来源进行了验证。     

上海市交通干道空气中苯系物冬季污染特征初探

2004年冬季对上海市交通干道附近空气中苯系物的浓度水平进行了监测,并采用气相色谱法进行分析。结果表明,采样期间大气中苯、甲苯、乙苯、二甲苯的浓度分别为1.77~27.7μg/m3、7.29~195μg/m3、3.11~40.2μg/m3、4.49~82.4μg/m3。每日6:30~9:30和15:30~19:00两个时段苯系物的浓度要高于中午时间的浓度,与国内其他城市相比,上海市甲苯的浓度要高,浓度水平要远远高于国外城市的测定结果。苯系物的浓度受风速和风向影响较大。提出了制订空气中苯系物的排污清单和加强机动车尾气中苯系物控制的建议。     

安徽某燃煤电厂周边土壤汞分布特征及风险评价

结合当地气象条件,采集了安徽某燃煤电厂周边地区的土壤,采用冷原子吸收法测定其汞含量,应用地统计学和地理信息系统方法分析了电厂周边表层土壤汞含量的空间分布特性,分析了土壤中汞与理化性质之间的相关性,并进行了风险评价。结果表明,电厂周边表层土壤汞含量范围为0.015~0.076 mg/kg,平均值为0.029 mg/kg,虽未超过国家允许的标准,但与当地背景值及安徽省土壤汞含量相比均有一定程度的增加;土壤汞含量的总体分布特征为除距排放源1~2 km的环形区域受影响最大外,污染程度随着与电厂距离的增大而递减,汞含量空间分布受主导风向影响呈现明显的条带分布。相比于单因子污染指数法和地累积指数法,潜在生态危害指数评价法能更好地反映燃煤电厂周围土壤中汞的污染水平和生态风险程度。土壤汞含量与土壤理化性质之间存在不同程度的相关性。     

典型铝塑厂周边土壤重金属分布特征与健康风险评价

为探究铝塑园区周边土壤重金属污染情况,选取山东省某城市塑料开发区为研究区,按照分层采样方式获取到80个土壤样品,分别测定土壤中As、Cd、Hg、Cr、Cu、Ni、Pb、Zn含量,运用统计分析法探讨土壤重金属等的分布特征和来源,并利用健康风险评价模型确定了土壤重金属对周边居民的健康风险。结果表明:As、Cd、Hg、Cr、Cu、Ni、Pb和Zn均超出山东省土壤背景值,其中Cd、Hg、Cu和Pb分别超出背景值48. 15%、106. 90%、62. 04%和39. 96%,表明土壤中存在一定程度的重金属积累,在周边140～210 m处最为严重,且受人类活动影响强烈,与风向关系不大;土壤重金属垂直分布特征大致呈现随着深度的增加不断增加,在20 cm深度附近达到最高值,其后不断降低并趋于平稳,Cd、Hg、Cu、Pb和Zn变异幅度大,受到人为干扰较大,As、Cr和Ni主要受成土母质控制,属于自然来源,变动幅度较小;研究区内8种元素不存在非致癌风险,Cr、As、Ni和Cd产生的致癌风险处在可接受范围内,但存在的潜在致癌风险应引起足够的重视。     

包头某铝厂周边土壤重金属污染及健康风险评价

以包头市某铝业周边500 m内土壤为研究对象,测定其东北、东南、西北、西南4个方向不同水平距离及深度处土样中Cu、Cd、Pb、Zn、Ni和Cr的含量,并采用地累积指数法和健康风险评价法对重金属污染状况进行评价。结果表明,该区域表层土壤中6种重金属普遍高于内蒙古土壤背景值,且在西南方向50 m处含量最高,人类活动对该区域重金属干扰强烈,而风向对重金属分布影响不大;铝厂周围土壤中Cd、Pb处于中污染-重污染,Cu和Ni处于无污染-中污染,Zn和Cr为无污染,各金属污染程度随土壤深度的增加而减轻;健康风险评价表明,研究区域内Cu、Pb、Ni和Cd均不存在非致癌健康风险,而Cd的致癌危害虽在可接受范围内,但已存在潜在致癌风险,Ni的致癌健康风险指数已超过预警值,应予以高度重视和防治。     

焦化废水中多环芳烃的成分谱及污染特征

液-液萃取-高效液相色谱法分析了焦化废水中EPA优先控制的16种多环芳烃含量,总结出其成分谱及污染特征。结果表明:16种多环芳烃在焦化废水中浓度差异较大,主要以在水中溶解度较大的萘、苊、芴、菲、荧蒽、芘为主。其中萘对多环芳烃总量的贡献最大,占总量的36.70%~86.78%。焦化企业排放废水中6种多环芳烃的总量无超标现象,苯并[a]芘单体超标较普遍。     

预冷冻浓缩系统与气相色谱-质谱法测定空气中苯的测量不确定度评定

根据 Top－down技术中的控制图法，运用预冷冻浓缩系统与气相色谱－质谱联用对苯标准样气进行多次测定。通过计算和评定，得出当苯的测定浓度为100×10^－9时，不确定度为5．1×10^－9。     

Characterization of ambient ozone and its precursors around a coking plant

The local-scale relationship between ambient ozone (O₃) and its precursors was examined around a coking plant in northern China. The upwind, plant boundary, and downwind locations were selected for investigation during the summer and autumn seasons in 2012. It was found that propene, toluene, and benzene were the top three non-methane hydrocarbon (NMHC) species for O₃ formation at plant boundary, while propene, toluene, and m/p-xylene were the top three NMHC species at downwind location. Isoprene was the dominant species for O₃ formation at upwind location. It was also found that an O₃ depressing process occurred at plant boundary as a result of high NO emissions. Both local photochemistry and transport led to O₃ accumulation at the downwind locations. The variation of NMHC concentration during O₃ polluted and non-polluted episodes was investigated, and it indicated that NMHC concentration was higher during non-polluted episodes than polluted episodes. The impacts of precursors on O₃ formation under different meteorological conditions were also examined.     

上海市臭氧污染时空分布及影响因素

分析2006—2016年上海市的监测数据发现,臭氧(O_3)浓度存在逐年上升趋势,污染持续时间有所增加,但除水平风速有下降趋势外,其他相关气象因素的年际变化趋势并不显著。空间分析结果表明,上海市O_3超标主要集中在西南部郊区,但市区O_3超标潜势不容忽视。O_3污染高发季节的污染玫瑰图分析发现,上海市南部地区是影响上海市O_3污染的关键区域;对于NO_2减排的影响分析发现,尽管上海市O_3平均浓度总体处于上升趋势,但在NO_2下降幅度最为明显的内环市区和北部郊区,O_3上升幅度低于NO_2下降幅度较小的内外环区域和西部郊区,表明上海市的O_3污染控制仍需持续推进NOx的减排,并同步推进VOCs的减排。     

焦化废水生化处理过程中溶解性有机物及毒性变化规律

焦化废水中的溶解性有机物(DOM)作为废水污染物和毒性的主要来源受到广泛关注。厌氧-缺氧-好氧(A-A-O)生物法联合混凝沉淀工艺在焦化废水处理中被广泛应用。于2018年4,7和11月分别采集4座焦化废水处理厂废水,采用光谱学分析手段和水生生物急性毒性试验对A-A-O联合混凝沉淀处理过程中焦化废水的DOM和毒性变化进行分析。结果表明,焦化废水中含有大量不饱和芳香性物质,其中类色氨酸、络氨酸物质占主导,其次为类溶解性微生物代谢产物、类富里酸物质和类腐殖酸类物质;未经处理的焦化废水对藻类和大型溞的急性毒性等级为中毒至高毒。A-A-O联合混凝沉淀处理可去除90%以上的类色氨酸、络氨酸和类富里酸物质,但对类腐殖酸类物质去除率相对较低,仅为约80%,关键去除段为缺氧段和好氧段;该工艺对焦化废水急性毒性削减率为80.51%~94.30%,关键削减段为厌氧段。Pearson相关性分析结果显示,焦化废水溶解性总有机碳(TOC)、类腐殖酸类物质荧光组分C1和类富里酸类物质荧光组分C4与废水急性毒性存在显著正相关关系,可利用其作为水样急性毒性初筛的指示性指标。可为焦化废水生化处理的效能优化和废水毒性控制及安全评估提供科学支撑。     

Distribution and health-risk of polycyclic aromatic hydrocarbons in soils at a coking plant

Nineteen soil samples were collected in and around Songshan coking plant in Guangdong province of China and analyzed for eighteen polycyclic aromatic hydrocarbons (PAHs) by gas chromatography-mass spectrometry (GC-MS). The total concentration of PAHs ranged from 2.36 to 1146.39 mg kg(-1) dry weight, varying significantly among the sampling sites, most individual PAHs were correlated with each other. A cluster analysis was performed to examine the correlation of PAH distribution, five groups were observed with sample types in the coking plant. 2-3 ring PAHs were predominant in group I and II, while 4-5 ring PAHs showed great abundance in group III, IV and V, which contributed to the distance from the emission sources in the coking plant and the behaviors of particle-bound and gaseous PAHs. The ratios of Flu?:?(Flu + Pyr), BaA?:?(BaA + Chr), InP?:?(InP + BgP) and Ant?:?(Ant + Phen) ratios were 0.51-0.87, 0.16-0.89, 0.47-0.68 and 0.03-0.60, respectively. The total index of all studied soils was > 6, indicating that the source of the PAHs in coking plant soils were from the pyrolysis processes. Health risk assessments were carried out by dermal PAH exposure data to quantify cancer risk. The resultant lifetime exposure levels due to TEQ(BaP) desorbed onto skin for workers ranged from 2.25 × 10(-7) to 7.86 × 10(-5) mg kg(-1) per day, and the estimated cancer risks were between 8.45 × 10(-6) and 2.94 × 10(-3), indicating that the dermal exposures of PAHs to coking workers might be acceptable in most soil sites.     

用蚕豆叶尖微核技术筛选对环境污染物敏感品种

为了筛选蚕豆叶尖微核监测技术敏感材料,以二甲苯为污染物,对甘肃产的10个蚕豆品种进行了测试。结果表明,蚕引8号微核出现率与二甲苯诱变剂浓度成正比,平均微核率差异极显著,是监测评价二甲苯污染的敏感品种。     

VOCs走航观测在城市污染源排查中的应用

为推进城市空气质量精细化管理工作的实施,实现VOCs污染源精准排查,2019年3-4月,利用单光子电离飞行时间质谱对青岛市重点区域进行了VOCs走航观测。在排查到的污染源中,工业区的VOCs浓度较生活区整体偏高,且生活区、工业区夜间的VOCs浓度均较白天高。VOCs各类组分中,生活区白天苯系物、卤代烃、烯烃、烷烃的占比均在20%左右,夜间苯系物占比明显升高;工业区苯系物在白天和夜间的占比均最高,其他组分相对较小。浓度较高的前10位VOCs物种中,生活区白天烯烃物种占主导,夜间烷烃物种的比重明显增加;工业区苯系物、烯烃物种在白天和夜间的比重均较大,烷烃物种较小。生活区VOCs的污染源主要为机动车尾气排放和油品挥发,工业区主要为企业排放。烯烃和苯系物臭氧生成贡献较烷烃高,特别是丁烯、戊烯、己烯、甲苯、二甲苯/乙苯、三甲苯贡献显著,建议作为优控物种重点管控。     

Multivariate statistical study of seasonal variation of BTEX in the surface water of Savitri River

Volatile organic compounds (VOCs) analysis was carried out for the surface water of the Savitri river during the period of June 2005 to June 2007. BTEX compounds (Benzene, Toluene, Xylene & Ethyl benzene) were analyzed by using micro extraction technique (Purge & Trap). Concentrations of these BTEX compounds were ranging from 0.1 to 1.5 ppm during sampling period. Higher concentrations of BTEX were found at sampling location VI. Concentration of ethyl benzene was very low as compare to other compounds. However, the concentration of benzene was very high. Seasonal variations in conc. of BTEX compounds were observed and higher concentration was detected during the summer season. Salting-out effect had given higher quantification values. In PCA and PFA, the component loading for all the variables are positively correlated. Death of fishes was observed in the river that is indication of severe pollution problem.     

Mixing ratios of carbonyls and BTEX in ambient air of Kolkata, India and their associated health risk

Mixing ratios of 15 carbonyls and BTEX (benzene, toluene, ethyl benzene, xylenes) were measured for the first time in ambient air of Kolkata, India at three sites from March to June 2006 and their photochemical reactivity was evaluated. Day and nighttime samples were collected on weekly basis. Formaldehyde was the most abundant carbonyl (mean concentration ranging between 14.07 microg m(-3) to 26.12 microg m(-3) over the three sites) followed by acetaldehyde (7.60-18.67 microg m(-3)) and acetone (4.43-10.34 microg m(-3)). Among the high molecular weight aldehydes, nonanal showed the highest concentration. Among the mono-aromatic VOCs, mean concentration of toluene (27.65-103.31 microg m(-3)) was maximum, closely followed by benzene (24.97-79.18 microg m(-3)). Mean formaldehyde to acetaldehyde (1.4) and acetaldehyde to propanal ratios (5.0) were typical of urban air. Based on their photochemical reactivity towards OH. radical, the concentrations of the VOCs were scaled to formaldehyde equivalent, which showed that the high molecular weight carbonyls and xylenes contribute significantly to the total OH-reactive mass of the VOCs. Due to the toxic effect of the VOCs studied, an assessment for both cancer risk and non-cancer hazard due to exposure to the population were calculated. Integrated life time cancer risk (ILTCR) due to four carcinogens (benzene, ethyl benzene, formaldehyde and acetaldehyde) and non-cancer hazard index for the VOCs at their prevailing level were estimated to be 1.42E-04 and 5.6 respectively.