Primary and secondary organic aerosol in an urban/industrial site: Sources, health implications and the role of plastic enriched waste burning

PM10 samples were collected from an urban/industrial site nearby Athens, where uncontrolled burning activities occur. PAHs, monocarboxylic, dicarboxylic, hydroxycarboxylic and aromatic acids, tracers from BVOC oxidation, biomass burning tracers and bisphenol A were determined. PAH, monocarboxylic acids, biomass burning tracers and bisphenol A were increased during autumn/winter, while BSOA tracers, dicarboxylic- and hydroxycarboxylic acids during summer. Regarding aromatic acids, different sources and formation mechanisms were indicated as benzoic, phthalic and trimellitic acids were peaked during summer whereas p-toluic, isophthalic and terephthalic were more abundant during autumn/winter. The Benzo[a]pyrene-equivalent carcinogenic power, carcinogenic and mutagenic activities were calculated showing significant (p < 0.05) increases during the colder months. Palmitic, succinic and malic acids were the most abundant monocarboxylic, dicarboxylic and hydrocarboxylic acids during the entire sampling period. Isoprene oxidation was the most significant contributor to BSOA as the isoprene-SOA compounds were two times more abundant than the pinene-SOA (13.4 ± 12.3 and 6.1 ± 2.9 ng/m³, respectively). Ozone has significant impact on the formation of many studied compounds showing significant correlations with: isoprene-SOA (r = 0.77), hydrocarboxylic acids (r = 0.69), pinene-SOA (r = 0.63),dicarboxylic acids (r = 0.58), and the sum of phthalic, benzoic and trimellitic acids (r = 0.44). PCA demonstrated five factors that could explain sources including plastic enriched waste burning (30.8%), oxidation of unsaturated fatty acids (23.0%), vehicle missions and cooking (9.2%), biomass burning (7.7%) and oxidation of VOCs (5.8%). The results highlight the significant contribution of plastic waste uncontrolled burning to the overall air quality degradation.     

大气中挥发性有机物在线监测系统

一种新型的监测大气中挥发性有机物（包括含氧挥发性有机物）的在线监测系统被研制,即将超低温冷阱捕集-热解析装置与气相色谱-质谱仪联用.其分析方法是大气样品经除水、除O3后以60 mL·min-1的流速通过温度为-150℃的超低温冷阱捕集5min,然后样品在110℃下解析后进入GC-FID/MS系统进行分析,时间分辨率为1h.系统使用混和标气进行标定.目标化合物定量曲线的R2值为0.9137~0.9998,相对标准偏差(RSD)均小于10%.将系统与相关商业化的VOC在线监测仪器进行比对,对于相同目标化合物进行分析,其相关系数r在0.7412~0.9620之间.     

气相色谱／质谱（GC／MS）联用在我国大气有机污染监测中的应用

概述ＧＣ／ＭＳ联用在我国大气有机污染监测中的应用，介绍大气中有机污染物，如多环芳烃、硝基多环芳烃、多氯二苯并二恶英、多氯二苯并呋喃、碳氢化合物、苯系物、恶臭、有机硫化合物、多组分有机污染物的测定。     

高效液相色谱串联质谱法直接测定环境水样中8种有机磷农药

建立了一种高效液相色谱-串联质谱法（LC-MS/MS）同时测定环境水样中8种有机磷农药的分析方法。以地表水、地下水、污水和废水样品作为代表性水样基底,前处理方法仅采用简单的滤膜过滤,在C₁₈柱分离后,在多反应监测模式下进行分析检测。结果表明,敌百虫、毒死蜱等有机磷农药在样品保存过程中迅速发生降解,分析须在样本采集后1 d内完成;该方法的检出限为0.10~0.20 μg/L,线性拟合相关系数（r）均>0.995;不同基底、不同浓度的加标回收实验表明,8种有机磷农药在环境基底中的回收率为74.5%~118%,相对标准偏差为0.4%~8.6%。该方法操作简便、灵敏度高、准确性好,在未来环境监测工作中具有较好的应用前景。     

Chemical and colloidal analyses of natural seep water collected from the exploratory studies facility inside Yucca Mountain,Nevada, USA

Yucca Mountain is being considered as a geological repository for the USA’s spent nuclear fuel and high-level nuclear waste. Numerous groundwater seeps appeared during March 2005 within the exploratory studies facility (ESF), a tunnel excavated in the mountain. Because of the relevance to radionuclide transport and unsaturated zone-modeling studies, we analyzed the seep samples for major anions and cations, rare earth elements, and colloids. Major ion species and elemental concentrations in seep samples reflect interaction of the water with the volcanic rock and secondary calcites. Elemental fractograms from flow-injection field-flow fractionation ICP–MS scans detected Br, Ca, Cl, Cu, Fe, I, Mg, Si, Sr, W, and U at void fractions, suggesting they may be present in the form of dissolved anions. Colloids approximately 10 nm in hydrodynamic diameter, possibly calcite, were also present in the seepage samples. Geochemical calculations indicate, however, these may be an artifact (not present in the groundwater) which arose because of loss of CO₂ during sample collection and storage.     

焦化厂A/O出水中的有机污染物分析

采用色谱－质谱（GC／MS）联用仪分析和鉴定了上海宝钢焦化厂A／O生化阶段出水的有机污染物组成,共检出各类有机污染物70多种。结合焦化废水专用混凝剂的混凝处理实验结果,指出了各类有机污染物的去除情况。     

农药残留速测技术研究进展

本文综述了国内外农药快速检测技术的研究状况。在速测技术中 ,色 -质联用分析法已发展得比较成熟 ,所得结果比较可靠 ,但该法的测定时间仍较长 ;免疫分析法具有简单、快速、价廉、特异性高、需样品量少等优点 ;生物传感器法更方便、快捷。     

液相色谱-串联质谱法同时测定污水中10种精神活性物质

建立了采用液相色谱-串联质谱法(LC-MS/MS)同时测定污水中10种精神活性物质的分析方法。污水样品经甲酸与甲酸铵调节pH后,加入氘代内标混匀,离心并过滤膜后可直接上样分析。研究表明,在1~250 ng/L的线性范围内,10种精神活性物质的线性相关系数均大于0.992,定量限均低于0.5 ng/L。在3个加标水平下,10种精神活性物质的加标回收率为87.2%~114%,相对标准偏差为0.53%~3.60%(n=3)。将该方法应用于某区域10份生活污水样品的检测,在3份水样中检出吗啡、甲基苯丙胺、氯胺酮等精神活性物质,对应的质量浓度范围分别为3.41~9.55、0.90~1.63、1.06~1.78 ng/L。与经固相萃取前处理后的分析方法相比,该方法可在10 min内完成分离和检测的全过程,具有简单、快速、节约的优点,可用于污水样品中10种痕量水平精神活性物质的定量分析。     

Tissue distribution of polychlorinated naphthalenes (PCNs) and non-ortho chlorinated biphenyls (non-ortho CBs) in harbour porpoises (Phocoena phocoena) from Swedish waters

Polychlorinated naphthalenes (PCNs) and non-ortho chlorinated biphenyls (non-ortho CBs) were analysed in blubber, nuchal fat, liver, muscle, kidney and brain of three male harbour porpoises (Phocoena phocoena) from the west coast of Sweden. To estimate spatial variation, PCNs and non-ortho CBs were analysed in six blubber samples collected at different anatomical sites of each animal. Highest wet weight concentrations of ΣPCNs were detected in the lipid rich tissues (blubber and nuchal fat) and liver (520–730 and 520 pg/g, respectively) and lowest in brain (22 pg/g). TetraCNs were most abundant in muscle, kidney and brain, while the hexaCNs were most abundant in the lipid rich tissues and liver. The highest lipid weight concentration recorded (11 ng/g) was for the hexaCN congeners no. 66/67 in liver. These coeluting hexaCN congeners accounted for 80–100% of total hexaCNs in all tissues examined.Concentrations of Σnon-ortho CBs were highest in lipid rich tissues (220–280 pg/g wet weight). Non-ortho CB no. 77 and 169 constituted between 62–86% and 4.9–9.3%, respectively, of total Σnon-ortho CBs. No major variation of Σnon-ortho CB concentrations was found between the six different blubber sites but higher ΣPCN concentrations (wet weight) were found dorsally at the peduncle. Toxic equivalent concentrations (TEQs) showed that non-ortho CB no. 126 was the main contributor to total TEQs in all tissues, except liver in which hexaCN congener nos. 66/67 contributed to about 50% of total TEQs.     

固相微萃取-气相色谱-质谱法测定地毯中总挥发性有机化合物

建立了一种固相微萃取与气相色谱质谱联用测定地毯中总挥发性有机化合物的方法,该方法简便快速,重现性好,分析结果同小型环境平衡舱法测定的结果比较吻合。