简化亚甲蓝法测定地表水中阴离子洗涤剂

根据甲蓝法测定地表水中阴离子洗涤剂的工作经验,对其分析过程中的标准曲线制作、PH调节、萃取等操作进行适当的简化,不但满足分析质量的要求,而且提高了监测工作效率,降低分析成本.     

经口摄入土壤多溴联苯醚生物可给性变化及影响因素的体外消化模拟

误食土壤是污染物(如多溴联苯醚)人体(主要是儿童)暴露的重要途径,人体消化道内污染物吸收的生物可给性是针对此种暴露方式进行定量风险评估的有效途径之一.本研究采用体外消化实验模拟3种不同有机碳含量的天然土壤中典型多溴联苯醚(BDE-28、BDE-47、BDE-99和BDE-153)在胃和小肠消化液中的释放,验证部分消化释放的多溴联苯醚因消化残留固相表面的再吸附造成低估实际生物可给性,并通过不同水土比的拟合计算予以校正.结果表明,校正后的消化率普遍高于校正前;就不同土样而言,BDE-28、BDE-47、BDE-99和BDE-153在不同初始暴露浓度条件下平均提升比例范围分别为14.3%~42.3%、11.1%~32.1%、4.9%~12.3%和0.0%~7.7%.因此,未经校正的消化率会显著低估PBDEs消化道内的生物可给性,尤其是低溴代组分及PBDEs初始浓度较高或高TOC含量的土样.校正后BDE-28、BDE-47、BDE-99和BDE-153的消化率分别维持在21.9%~54.7%、18.8%~43.1%、13.4%~27.2%和9.3%~19.9%.此外,PBDEs的消化率与其辛醇-水分配系数的对数lg KOW呈显著负相关;而与土壤TOC含量及PBDEs初始暴露浓度的相关性并不显著,尤其是高溴代组分.     

Contribution of precursor compounds to the release of per- and polyfluoroalkyl substances (PFASs) from waste water treatment plants (WWTPs)

Per-and polyfluoroalkyl substances(PFASs) are ubiquitous in sludge and water from waste water treatment plants, as a result of their incorporation in everyday products and industrial processes. In this study, we measured several classes of persistent PFASs,precursors, transformation intermediates, and newly identified PFASs in influent and effluent sewage water and sludge from three municipal waste water treatment plants in Sweden, sampled in 2015. For sludge, samples from 2012 and 2014 were analyzed as well.Levels of precursors in sludge exceeded those of perfluoroalkyl acids and sulfonic acids(PFCAs and PFSAs), in 2015 the sum of polyfluoroalkyl phosphoric acid esters(PAPs) were 15–20 ng/g dry weight, the sum of fluorotelomer sulfonic acids(FTSAs) was 0.8–1.3 ng/g,and the sum of perfluorooctane sulfonamides and ethanols ranged from non-detected to 3.2 ng/g. Persistent PFSAs and PFCAs were detected at 1.9–3.9 ng/g and 2.4–7.3 ng/g dry weight, respectively. The influence of precursor compounds was further demonstrated by an observed substantial increase for a majority of the persistent PFCAs and PFSAs in water after waste water treatment. Perfluorohexanoic acid(PFHxA), perfluorooctanoic acid(PFOA), perfluorohexane sulfonic acid(PFHxS), and perfluorooctane sulfonic acid(PFOS)had a net mass increase in all WWTPs, with mean values of 83%, 28%, 37% and 58%,respectively. The load of precursors and intermediates in influent water and sludge combined with net mass increase support the hypothesis that degradation of precursor compounds is a significant contributor to PFAS contamination in the environment.     

Arsenic biotransformation and an arsenite S-adenosylmethionine methyltransferase in plankton

<正>Arsenic(As)is a well-recognized toxicant and carcinogen.Chronic exposure to inorganic arsenic causes a range of human cancers(e.g.,skin,bladder,and lung)and increases the risk of developing diabetes,hypertension,and cardiovascular and neurological diseases.The prevalence of arsenic species and the severity of their health effects continue to drive and demand for extensive research(Carlin et al.,2016).     

小型城市污水排放量预测模型研究——以楚雄市为例

针对小城市污水排放量历史数据较少,城市发展变化较大的特点,以楚雄市为例,提出了基于污水排放来源以及生成机理的预测方法。根据历史人口增长趋势以及城镇化率进行城区人口综合预测,运用定额法根据不同行业用水特点预测城市用水量,结合城市污水排放特点对楚雄市近期以及远期城市污水排放量进行科学合理的预测,并对预测结果进行了分析,可为城市发展规划提供决策参考。     

北仑区臭氧与挥发性有机物关系研究

利用2016年夏季北仑区域的VOCs及臭氧在线监测结果,研究了北仑区域VOCs的浓度水平、组成及来源情况,同时还分析了区域的臭氧生成与VOCs之间的关系.结果表明:北仑的VOCs浓度整体水平与一些大城市相比较低,在VOCs组成中比例最高的为烷烃,臭氧生成潜势(OFP)贡献最高的为芳香烃;北仑的VOCs来源与北京和上海均有所不同,且北仑的机动车对VOCs的贡献特征值B/T为0.56,超过了临界值;北仑区域的臭氧生成主要是由本地的VOCs等的臭氧前驱体通过光化学反应生成.     

关于抑尘剂开发及其存在主要问题的探讨

基于化学抑尘剂与粉尘之间的润湿、粘结、凝聚作用机制,综述了近年来各类化学抑尘剂的合成技术及原理,概述了化学抑尘剂在矿山粉尘抑制中的应用现状,并对化学抑尘剂研究方向的主要问题和应用前景进行了探讨。     

Homogeneous and heterogeneous reactions of anthracene with selected atmospheric oxidants

The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol (SOA) formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer (SMPS) during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). Gas chromatograph/mass spectrometer (GC/MS) analyses of oxidation products of anthracene were carried out for assigning the time-of-flight (TOF) mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10- dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO.     

废气中铅烟(尘)排放浓度测量分析的不确定度

通过对废气中铅及其化合物排放浓度测量的过程分析,将环境污染源监测中现场采样与实验室分析有机结合,分析并评定监测全过程的不确定度,为提高废气中污染物排放测量的准确性提供了科学的依据.     

二氧化氮与相关室内空气品质问题的研究综述

二氧化氮是室内空气的主要污染物之一。从技术层面上介绍了室内空气的二氧化氮采集与测量方法,重点介绍了被动式采样法、分光光度法、化学发光法和库伦原电池法。详细分析了影响室内二氧化氮浓度的主要因素及室内二次污染的相关研究,归纳了其对人类健康的不良影响,并提出室内二次污染是未来的重要研究方向。