典型污染源材料中多溴联苯醚(PBDEs)的释放

为研究以多溴联苯醚（PBDEs）为代表的含卤半挥发性有机物（SVOCs）在室内空气中的扩散特性,在对杭州室内环境（办公室、居室）空气中PDBEs14种单体浓度检测的基础上,分析比较了不同污染源材料中PBDEs的含量,测定了材料PBDEs挥发强度系数;探究了典型污染源材料中PBDEs释放的影响因素及其相关性.结果表明,杭州室内环境空气颗粒相和气相中PBDEs平均浓度为427.26和416.46pg/m³,其中颗粒相和气相中主要特征单体均为BDE-209.所选取的9种室内常用材料的PBDEs挥发强度系数大小依次为：地毯>电线>塑料板>阻燃布>电路板>防烫桌布>保温棉>自粘墙纸>绝缘胶带.对比不同材料中各PBDEs同系组的含量：绝缘胶带、塑料板、防烫桌布、阻燃布中十溴二苯醚（deca-BDEs）的占比最高,分别为81.33%、63.83%、27.3%和34.1%;电线中四溴二苯醚（tetra-BDEs）的占比最高,为29.83%;自粘墙纸、电路板、地毯、保温棉中五溴二苯醚（penta-BDEs）的占比最高,分别为35.82%、41.25%、45.75%和38.64%.典型污染源材料中PBDEs释放的影响因素实验结果表明,环境模拟舱中的PBDEs总浓度与温度和封闭时间对数均呈显著正相关,相关系数r和显著水平P分别为r=0.811,p<0.05和r=0.883,p<0.05,且封闭时间对源释放PBDEs总浓度的影响比温度稍大.同时,污染源特征因素（材料中PBDEs的固有含量与PBDEs挥发强度系数）对源释放的影响程度比环境因素（温度和封闭时间）大.     

冬季天津家庭室内空气颗粒物中邻苯二甲酸酯污染研究

为了解我国家庭住宅室内空气颗粒物中邻苯二甲酸酯的污染程度,采集天津市13户家庭住宅冬季室内空气颗粒物PM10、PM2.5样品,采用GC/MS分析了DMP、DEP、DBP、BBP、DEHP、DOP等6种邻苯二甲酸酯.结果表明,室内空气颗粒物中DMP、DEP、DBP、BBP、DEHP这5种邻苯二甲酸酯在所有家庭均被检出,DOP在部分家庭检出.其中,DBP和DEHP为主要污染物.PM10和PM2.5中的6种物质占ΣPAEs颗粒相的比例规律相同,DBP和DEHP较大,分别为13.92%～91.50%、5.56%～85.08%和20.88%～93.95%、5.53%～75.90%;其次是DMP、DEP和BBP,DOP最小.不同粒径颗粒物上PAEs的分布显示,大多数PAEs易吸附在粒径较小的细粒子PM2.5上;结合调查问卷分析表明,冬季室内空气颗粒物上PAEs污染主要来源于室内,受房间的装修时间、装修特点、生活习惯、吸烟、烹饪、塑料制品使用量、室内清洁度和温度等因素的影响.     

大学校园室内环境PM2.5中PAEs污染特征及暴露风险

为揭示大学校园室内环境中PM_2.5及其中PAEs（phthalate esters,邻苯二甲酸酯）的污染特征和师生暴露风险,以陕西师范大学长安校区为例,采集了校园秋冬季6个采样点52个室内PM_2.5样品,利用气相色谱质谱联用仪检测了其中22种PAEs的浓度,分析了其构成和时空分布,评估了师生暴露健康风险.结果表明:①不同采样点PM_2.5中22种PAEs的总浓度范围为237~413 μg/m3,其中6种优控PAEs的总浓度范围为4.81~7.47 μg/m3;室内PM_2.5中的PAEs主要为邻苯二甲酸二异丁酯、邻苯二甲酸二环己酯和邻苯二甲酸二异壬酯,均为非优控PAEs,且这3种单体的浓度远高于6种优控PAEs单体的浓度.②各采样点检出的6种优控PAEs单体不同,图书馆和教室中6种优控PAEs均被检出,宿舍中检出4种,家属区中检出3种.③季节变化对室内PM_2.5浓度及其中的PAEs浓度均会产生影响,冬季室内PM_2.5平均浓度（58.3 μg/m3）高于秋季（55.4 μg/m3）,12月6种优控PAEs单体浓度范围为0.250~3.86 μg/m3,明显高于其他月份.④来源解析表明,校园室内空气PM_2.5中的PAEs主要来自室内装饰材料的释放,学生油墨及化妆品和个人护肤品的使用,以及增塑剂的使用及涂层的释放.⑤6种优控PAEs对人体产生的非致癌风险均较低,邻苯二甲酸丁基苄基酯和邻苯二甲酸二（2-乙基己基）酯的致癌风险均低于标准限值（1×10-6）,二者的致癌风险均可忽略.研究显示,校园内不同室内环境中PM_2.5污染程度及其中的PAEs浓度和构成均存在一定差异,师生暴露于室内空气PM_2.5中6种优控PAEs的非致癌风险均较低,致癌风险可忽略,但环境中非优控PAEs的污染与风险应给予足够的关注.      

夏季学生宿舍室内降尘中PAEs污染特征和暴露评价

利用CH2Cl2和超声对35个南开大学学生宿舍室内降尘样品中的DMP、DEP、DBP、BBP、DEHP 和DOP等6种PAES进行提取分离,采用GC-MS定量分析,研究了PAEs污染变化特征及暴露风险.结果表明,南开大学学生宿舍室内降尘中PAEs污染以DEHP和DBP为主,中位值浓度分别为126.916μg/g和123.591μg/g,两者之和占Σ6PAEs浓度的99%以上,室内降尘中PAEs污染程度和类型与室内含增塑剂产品的数量、室内清洁通风情况及成员性别有关;经口暴露水平大于皮肤,其中DBP、DEHP的暴露量高于美国,占人体总PAEs摄入量比例较高,故学生宿舍降尘中PAEs暴露应给予重视.     

Determination of 15 phthalate esters in air by gas-phase and particle-phase simultaneous sampling

Based on previous research, the sampling and analysis methods for phthalate esters (PAEs) were improved by increasing the sampling flow of indoor air from 1 to 4 L/min, shortening the sampling duration from 8 to 2 hr. Meanwhile, through the optimization of chromatographic conditions, the concentrations of 9 additional PAE pollutants in indoor air were measured. The optimized chromatographic conditions required a similar amount of time for analysis as before, but gave high responsivity, the capability of simultaneously distinguishing 15 kinds of PAEs, and a high level of discrimination between individual sample peaks, as well as stable peak generation. The recovery rate of all gas-phase and particle-phase samples of the 15 kinds of PAEs ranged from 91.26% to 109.42%, meeting the quantitative analysis requirements for indoor and outdoor air sampling and analysis. For the first time, investigation of the concentration levels as well as characteristics of 15 kinds of PAEs in the indoor air from four different traffic micro-environments (private vehicles, busses, taxis and subways) was carried out, along with validation of the optimized sampling and analytical method. The results show that all the 9 additional PAEs could be detected at relatively high pollution levels in the indoor air from the four traffic micro-environments. As none of the pollution levels of the 15 kinds of PAEs in the indoor air from the 4 traffic micro-environments should be neglected, it is of great significance to increase the types of PAEs able to be detected in indoor air.     

Pollution characteristics of 15 gas- and particle-phase phthalates in indoor and outdoor air in Hangzhou

Phthalate esters (PAEs), typical pollutants widely used as plasticizers, are ubiquitous in various indoor and outdoor environments. PAEs exist in both gas and particle phases, posing risks to human health. In the present study, we chose four typical kinds of indoor and outdoor environments with the longest average human residence times to assess the human exposure in Hangzhou, including newly decorated residences, ordinary residences, offices and outdoor air. In order to analyze the pollution levels and characteristics of 15 gas- and particle-phase PAEs in indoor and outdoor environments, air and particulate samples were collected simultaneously. The total PAEs concentrations in the four types of environments were 25,396, 25,466.8, 15,388.8 and 3616.2?ng/m³, respectively. DEHP and DEP were the most abundant, and DMPP was at the lowest level. Distinct variations in the distributions of indoor/outdoor, gas/particle-phase and different molecular weights of PAEs were observed, showing that indoor environments were the main sources of PAEs pollution. While most PAEs tended to exsit in indoor sites and gas-phase, the high-molecular-weight chemicals tended to exist in the particle-phase and were mainly found in PM_2.5. PAEs were more likely adsorbed by small particles, especially for the indoor environments. There existed a good correlation between the particle matter concentrations and the PAEs levels. In addition, neither temperature nor humidity had obvious effects on the distributions of the PAEs concentrations.     

Pollution levels and characteristics of phthalate esters in indoor air of offices

The pollution status and characteristics of PAEs (phthalate esters) were investigated in indoor air of offices, and PAEs of both gas-phase and particulate-phase were detected in all the samples. The concentration (sum of the gas phase and the particulate phase) was 4748.24 ng/m³, ranging between 3070.09 and 6700.14 ng/m³. Diethyl phthalate, dibutyl phthalate, and di(2-ethylhexyl) phthalate were the most abundant compounds, together accounting for 70% of the ∑ 6PAEs. Dividing the particulate-phase PAEs into four size ranges (< 2.5, 2.5–5, 5–10, > 10 μm), the result indicated that PAEs in PM_2.5 were the most abundant, with the proportion of 72.64%. In addition, the PAE concentration in PM_2.5 correlated significantly with the total particulate-phase PAEs (R² = 0.85). Thus, the amount of PAEs in PM_2.5 can be estimated from the total amount of particulate-phase PAEs using this proportion. In a comparison between the offices and a newly decorated study room, it was found that pollution characteristics were similar between these two places. Thus, it is implied that the PAE concentration decreased by 50% 2 yr after decorating.     

废旧塑料处置地沉积物中邻苯二甲酸酯污染特征及其生态风险

为了解废旧塑料处置活动对区域水体的影响,采用气相质谱联用仪(GC-MS),对河北省某废旧塑料处置地沉积物中16种PAEs(phthalate esters,邻苯二甲酸酯)的污染特征和生态风险进行了研究. 结果表明:研究样地的w(∑₁₆PAEs)为0.527~102 μg/g, 平均值为18.9 μg/g,其中,DEHP〔邻苯二甲酸(2-乙基己基)酯〕是PAEs最主要的污染单体,平均占w(∑PAEs)的66.6%. 对该处置地的污染物源分析表明,沉积物中PAEs主要来源于废旧塑料回收利用过程中的环境排放. 沉积物中w(DEHP)(14.2 μg/g)和w(DBP)(1.41 μg/g)(DBP为邻苯二甲酸二正丁酯)均超过各自环境风险限值(ERLs),w(DIBP)(DIBP为邻苯二甲酸二异丁酯)超过了美国华盛顿州颁布的沉积物质量警戒限值(0.610 μg/g). 研究显示,沉积物中DBP对鱼类的生态风险及DEHP对藻类和鱼类的生态风险水平不可接受,应引起足够重视.      

住宅室内降尘中邻苯二甲酸酯污染特征及暴露评价

利用CH2Cl2和超声对天津市13户家庭住宅冬季和夏季26个室内降尘样品中6种邻苯二甲酸酯(DMP、DEP、DBP、BBP、DEHP、DOP)进行提取分离,并采用气相色谱-质谱定量分析,研究了邻苯二甲酸酯污染变化特征和暴露风险.结果表明,冬夏两季,室内降尘样品均以DEHP 浓度最大,DBP第二,且DBP 和DEHP之和占ΣPAEs 的比例达到80.0%以上;冬季,各采样点6种邻苯二甲酸酯总含量(∑PAEs)浓度在1.498~32.587μg/g之间,平均浓度为(6.772±8.154)μg/g;夏季,∑PAEs浓度在1.981~40.041μg/g之间,平均浓度为(13.406±12.911) μg/g;PAEs浓度季节变化差异显著,夏季降尘样品中PAEs浓度高于冬季.暴露评价显示儿童和成人的夏季邻苯二甲酸酯总暴露量均大于冬季;经口暴露水平大于皮肤;平均儿童的暴露水平是成人的10倍左右;成人和儿童对4种物质(DBP、DEHP、DEP、BBP)的总暴露量最大值均出现在夏季;天津室内降尘暴露量与我国6城市室内降尘总暴露水平相当(除DEHP外),与德国和美国的暴露水平相比,天津儿童和成人的暴露量偏小.但是,室内环境中PAEs污染对人体健康的影响仍要引起重视,尤其是对低龄儿童的健康危害.     

邻苯二甲酸酯暴露的大鼠尿液生物标志物研究

建立了检测尿液中邻苯二甲酸酯类化合物(PAEs)共同水解产物邻苯二甲酸(PA)的分析方法;通过雄性成年SD大鼠代谢试验,检测了邻苯二甲酸二丁酯(DBP)和邻苯二甲酸二(2-乙基己基)酯(DEHP)单独暴露、以及联合暴露条件下大鼠尿液中PA总量,并分析了PA与暴露总量之间的关系.结果显示,随着暴露剂量的增大,尿液中排出的PA总量也不断增大;DBP单独暴露、DEHP单独暴露以及两者联合暴露时尿液PAEs代谢物平均排泄总量占摄入量的百分比分别为65.04%、55.00%和38.35%;大鼠尿液中PA的摩尔总量与DBP、DEHP、以及两者联合暴露的摩尔量之间的相关系数分别为0.92(P<0.01)、0.56(P<0.01)、0.93(P<0.01).尿液水解后的PA能够反映PAEs类物质的总暴露水平,将来可能作为一种潜在的暴露生物标志物用于人群的PAEs暴露监测.     

基于变权集对分析的室内空气品质的评价研究

对室内中的污染物浓度进行测量,科学评价室内空气品质.分析了室内空气质量七种污染物的浓度、评价等级、权重系数三个基本要素.通过建立集对分析模型,用联系度来描述评价对象与评价标准的同异程度,评价结果清晰地显示了集合之间的关系结构.在已有基本权重的基础上,引入变权公式,使污染物的浓度随评价等级同步动态变化.并用该方法对某小区的四栋楼的室内空气质量进行综合评价,该分析结果更加科学合理.该评价方法对室内空气质量评价更加全面、直观.     

Relationships between indoor and outdoor air quality in four naturally ventilated offices in the United Kingdom

Three offices in central London and one at a rural location were characterized with respect to air quality. All four offices were naturally ventilated. The characterization was supplemented by using a mobile laboratory to monitor the outdoor air quality. Results indicate that indoor pollutant concentrations may be up to 80% of the concentration outdoors but can greatly exceed outdoor concentrations. Additionally, it has been shown that indoor pollutants usually follow outdoor pollutant trends at lower levels, with only a small time delay due to mixing and dilution factors. The interaction between indoor and outdoor air is discussed with respect to ventilation characteristics and pollutant sources. A comparison between actual and modelled carbon dioxide levels may provide a useful indicator of ventilation.     

污染源位置对气体污染物影响的数值模拟

在自然通风、置换通风和单侧送侧回式通风3种方式下,通过改变污染源位置,运用CFD软件模拟研究了办公室内苯污染物的浓度分布规律,比较得出最佳通风方式下的最合理污染源位置。结果表明,3种通风方式下污染源放置的最合理位置是点3;苯污染源处于位置3时,3种通风方式中自然通风各平面苯污染物平均浓度普遍相对最高,而单侧送侧回方式的相对最低,置换通风居于二者之间。最终确定单侧送侧回通风方式下污染源处于位置3时为最佳物理模型,在该模型下办公室内通风效果最好,能够有效地排出室内气体污染物。因此,不同污染源位置对办公室内空气品质的影响不同。     

典型室内公共场所灰尘中PBDEs污染特征及源解析

为探索以多溴联苯醚（PBDEs）为代表的半挥发性有机化合物在典型室内公共场所中的污染特征及与材料的关系,在网咖、电子市场、建材市场、商场和图书城5类典型公共场所采集分析了灰尘样品,利用环境模拟舱研究了不同污染源材料中PBDEs的挥发强度系数（K_vsPBDEs）、衰减半衰期,结合主成分分析（PCA）分析了PBDEs的浓度与不同室内材料间的关系.结果表明,杭州5类典型室内公共场所灰尘中∑₁₄PBDEs的平均值分别为：网咖（2471.75ng/g）>电子市场（1071.77ng/g）>建材市场（900.63ng/g）>商场（441.27ng/g）>图书城（243.36ng/g）.所选取的10种室内典型污染源材料中∑₁₄PBDEs含量最高的为保温棉（91.61μg/g）,最低的为电路板（7.97μg/g）;K_vsPBDEs最高的为电线[14.04×10⁴μg/（g·m²）],最低的是纤维墙纸[0.87×10⁴μg/（g·m²）];塑料地毯、保温棉和纤维墙纸在40℃下的衰减半衰期分别为192,375和61d.研究发现室内公共场所中PBDEs的浓度与不同材料有关：网咖中PBDEs主要来自于纤维墙纸和电线;超市和图书城中PBDEs主要来自于陶瓷阻燃布和混纺地毯;建材市场中PBDEs主要来自于保温棉、电路板和塑料墙纸;电子市场中PBDEs主要来自于纤维阻燃布和电线.     

西安市住宅室内空气污染物实测分析与叠加效应

为了解居民住宅室内空气污染现状和保障公众健康,于2017年12月～2020年12月对西安市住宅小区830户居民住宅室内污染物[甲醛、苯、甲苯、二甲苯、总挥发性有机物(TVOC)、乙酸正丁酯、乙苯、苯乙烯和十一烷]浓度进行了实测分析和健康效应评估,并对污染物的叠加作用进行了分析.结果表明,室内甲醛、苯、甲苯、TVOC和二...     

滹沱河冲洪积扇地下水中酞酸酯的污染现状与分布特征

2014年9月采集石家庄地区滹沱河冲洪积扇地下水水样,采用气相色谱-质谱法测定了US EPA优先控制的6种酞酸酯(PAEs),对PAEs分布特征与风险进行了分析.结果表明,研究区内51个点位仅1个点位未检出PAEs,检出的ΣPAEs范围为nd~28 873.1 ng·L~(-1),与国内其他研究区相比,研究区地下水中PAEs污染水平较重.PAEs及各组分的空间分布存在显著差异.3个地下水单元PAEs的平均污染水平总体表现为山间沟谷河谷裂隙孔隙水单元(G1)滹沱河冲洪积扇扇顶部孔隙水单元(G2)滹沱河冲洪积扇扇中部孔隙水单元(G3).在G2、G3单元共计39个点位中,有23个点位地下水中的PAEs以邻苯二甲酸甲酯(DMP)为主,而其余点位均因临近周边污染源,地下水中PAEs含量较高,且以邻苯二甲酸(2-乙基己基)酯(DEHP)、邻苯二甲酸丁酯(DBP)为主.研究区人群饮用受PAEs污染地下水的总非致癌风险指数和总致癌风险指数范围分别为7.6×10-9~1.1×10-2、nd~1.2×10-6,均小于US EPA推荐的可接受的水平,风险较小.     

承德市室内环境质量污染现状调查与研究

对承德市160家宾馆、饭店、歌舞厅等公共场所,80个民用建筑工程项目,80余家个人家庭装修进行室内环境检测,发现不同场所室内主要超标污染物不同,新建公共场所主要超标污染物为挥发性有机物、甲醛;已建成的重点公共场所空气超标污染物主要为茵落总数和CO2;民用建筑工程超标污染物主要为氨、甲醛;个人家装超标污染物主要为总挥发性有机物,甲醛。     

Investigation of exhaled pollutant distribution in the breathing microenvironment in a displacement ventilated room with indoor air stability conditions

This study experimentally studied the dispersion of exhaled pollutant in the breathing microenvironment (BM) in a room equipped with a displacement ventilation (DV) system and indoor air stability conditions (i.e., stable and unstable conditions). The vertical temperature differences and the carbon dioxide (CO₂) concentration in the BM were measured. Results show that when DV is combined with the stable condition (DS), pollutant tends to accumulate in the BM, leading to a high pollutant concentration in this region. Whereas, when DV is combined with the unstable condition (DU), pollutant diffuses to a relatively wider area beyond the BM, thus the pollutant concentration in the BM is substantially reduced. Moreover, increasing the flow rate can reduce the pollutant concentration in the BM of the DS but yields little difference of the DU. In addition, personal exposure intensity increases with time, and the DS has a relatively higher increase rate than DU. The results suggest that indoor air stability will affect the performance of DV systems. DS will lead to a higher health risk for people when they stay in the indoor environment with pollutant sources, and DU is recommended for minimizing pollutant level in the BM in order to reduce the pollutant concentration and providing better air environments for the occupants.     

泉州湾邻苯二甲酸酯的地球化学特征

于2013年10月和2014年3月采集泉州湾表层海水、沉积物和生物体样品,采用气相色谱-质谱(GC-MS)联用技术对16种邻苯二甲酸酯(PAEs)进行定性、定量分析,研究泉州湾海水、沉积物及生物体中16种邻苯二甲酸酯(phthalate esters,PAEs)的含量分布、化学组成及环境意义。结果表明,研究的16种邻苯二甲酸酯类化合物中,表层海水、悬浮颗粒物(SPM)、表层沉积物以及牡蛎样品中均检出邻苯二甲酸二甲酯(DMP)、邻苯二甲酸二乙酯、邻苯二甲酸二异丁酯(DiBP)、邻苯二甲酸二丁酯(DBP)、邻苯二甲酸(2-乙基己基)酯(DEHP)和邻苯二甲酸二环己酯(DCHP);泉州湾表层海水中邻苯二甲酸酯溶解态总含量(PAEs)在1059.78~5893.17 ng/L之间,平均值为2996.82 ng/L,悬浮颗粒态总含量在11.09~270.39 g/g之间,平均值为110.47 g/g,表层沉积物中PAEs在206.6~464.2 g/kg之间,平均值为348.2 g/kg,生物体牡蛎中PAEs在179.29~254.24 g/kg之间,平均值为216.77 g/kg;DiBP、DBP和DEHP为PAEs的主要成分。与其他地区比较,泉州湾海洋环境中PAEs总体污染水平处于中等偏低水平。     

典型设施农业土壤酞酸酯污染特征及其健康风险

采用超声提取、气相色谱-质谱技术和CalTOX模型,分析了南京城郊典型设施菜地土壤中6种酞酸酯的污染特征、污染负荷及其健康风险.结果表明,所有的土壤样品中均检测出酞酸酯,6种酞酸酯的总量为0.15~9.68mg/kg,其平均含量为2.21mg/kg;邻苯二甲酸二丁酯(DnBP)、邻苯二甲酸(2-乙基己基)酯(DEHP)和邻苯二甲酸二辛酯(DnOP)为该地区设施农业土壤的主要酞酸酯种类,其检出率分别为88.2%、100%和79.8%,含量范围分别在n.d.~1.83、0.02~9.03、n.d.~1.74mg/kg之间;土壤pH值和有机碳含量与土壤酞酸酯含量之间无显著相关性,研究区域土壤酞酸酯总体污染负荷为4.31kg/hm2;健康风险评价结果表明DnBP和DEHP的潜在健康风险较高,设施农业从业者的主要暴露途径通过皮肤接触;设施菜地土壤酞酸酯含量、污染负荷以及健康风险均显著高于周边地区露天菜地土壤.