水环境中痕量有机有害物质的监测

论述了水中有机有害物质的监测,实质上是一项复杂系统的痕量分析课题。重点评述了痕量富集、色谱分离与监测、综合分析的主要进展。     

上海市大气PM2.5中溶剂可抽提有机物的特征研究

利用溶剂抽提、分离、毛细管气相色谱-质谱联用技术对2000年10月至2001年8月上海市5个不同功能区采集的大气PM_(2.5)样品中的溶剂可抽提有机物进行了检测,共检测出正构烷烃、单环芳烃、多环芳烃、有机酸、有机醇、有机酯等各类溶剂可抽提有机化合物267种。检出的82种多环芳烃中有15种属于美国EPA优先控制污染物名单。比较了不同季节、不同区域PM_(2.5)样品中正构烷烃、多环芳烃等化合物分布特征的差异。检出的喹啉类含氮杂环类化合物以及有机酸等污染物表现出一定的机动车排放特征。     

生物法净化废气中低浓度挥发性有机物的过程机理研究

 针对生物法净化低浓度挥发性有机废气的过程机理研究表明，生物膜填料塔净化低浓度甲苯气体是一个以气膜控制为主的传质过程，其中甲苯的生化降解属于瞬时快速化学反应，即甲苯的生化降解反应速率远远超过甲苯在液膜中的扩散速率，甲苯的生化降解在气液相界面处即可发生，其宏观表现即为甲苯气体直接吸附在润湿的生物膜上后迅速被微生物生化降解。因此，可以从气体吸附理论的新角度去解释生物法净化废气中低浓度挥发性有机物的动力学过程。对于低浓度挥发性有机废气的生物法净化装置的设计与操作而言，凡能改善传质条件、减少气膜阻力的措施均能强化这一生物吸收净化过程。     

一种新的拓扑指数及其在有机化合物结构/性质相关性研究中的应用

以距离矩阵为基础，提出一种表征化合物分子结构的拓扑指数，并将其用于预报饱和链烃类、醇类和含氮芳香类化合物的性质和活性，获得了满意的结果。     

毛细管柱气相色谱质谱法分析优先监测物的质量控制研究——Ⅰ.半挥发性有机物

报道了毛细管柱气相色谱质谱联用(GC-MS)方法分析半挥发性有机物的质量控制研究结果.对分析的全过程提出了质量控制标准.应用同位素标记内标物(IS),替代掺样物(SS)和基质掺样/重复基质掺样(MS/MSD)的回收率来判断样品处理与分析结果的可靠性.根据77种目标化合物,特别是标定检验化合物(CCC)和系统检验化合物(SPCC)的响应系数范围,确定GC-MS系统的工作状态和最终结果的正确性.给出了满足质量控制标准的12个土壤样品的结果.     

有机锡化合物测定方法研究进展

总结了有机锡化合物常用的测定方法，包括气相色谱－火焰光度法，气相色谱与原子吸收联用，气相色谱－微波等离子体发射光谱法，气相色谱－质谱法以及液相色谱与名种检测方法联用等。对样品前处理、衍生化方法、色谱分离及测定等也进行了讨论     

Production of hydrogen by steam gasification of dehydrochlorinated poly(vinyl chloride) or activated carbon in the presence of various alkali compounds

Steam gasification of dehydrochlorinated poly(vinyl chloride) (PVC) or activated carbon was carried out in the presence of various alkali compounds at 3.0 MPa and 560°C–660°C in a batch reactor or in a semi-batch reactor with a flow of nitrogen and steam. Hydrogen and sodium carbonate were the main products, and methane and carbon dioxide were the minor products. Yields of hydrogen were high in the presence of sodium hydroxide and potassium hydroxide. The acceleration effect of the alkali compounds on the gasification reaction was as follows: KOH > NaOH > Ca(OH)₂ > Na₂CO₃. The rate of gasification increased with increasing partial steam pressure and NaOH/C molar ratio. However, the rate became saturated at a molar ratio of NaOH/C greater than 2.0.     

生物净化挥发性有机化合物(VOCs)的研究进展

有机废气中大多含有低浓度的苯、甲苯、苯乙烯、多环芳烃等挥发性有机化合物(VOCs)。这类挥发性有机化合物会对人体健康和生态环境造成危害。治理VOCs污染是大气污染治理的重要部分。生物法处理有机废气具有运行费用低、没有二次污染等优点。常用的生物处理技术主要有生物过滤池、生物滴滤池和生物洗涤塔。20世纪80年代生物法在欧洲得到快速发展,我国于90年代以后也开始了生物处理VOCs废气的研究,并取得了一定的成就。     

Precursors and potential sources of ground-level ozone in suburban Shanghai

• Air masses from Zhejiang Province is the major source of O₃ in suburban Shanghai. • O₃ formation was in VOC-sensitive regime in rural Shanghai. • O₃ formation was most sensitive to propylene in rural Shanghai. A high level of ozone (O₃) is frequently observed in the suburbs of Shanghai, the reason for this high level remains unclear. To obtain a detailed insight on the high level of O₃ during summer in Shanghai, O₃ and its precursors were measured at a suburban site in Shanghai from July 1, 2016 to July 31, 2016. Using the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model and concentration weighted trajectories (CWT), we found that Zhejiang province was the main potential source of O₃ in suburban Shanghai. When the sampling site was controlled by south-western winds exceeding 2 m/s, the O₃-rich air masses from upwind regions (such as Zhejiang province) could be transported to the suburban Shanghai. The propylene-equivalent concentration (PEC) and ozone formation potential (OFP) were further calculated for each VOC species, and the results suggested that propylene, (m+p)-xylene, and toluene played dominant roles in O₃ formation. The Ozone Isopleth Plotting Research (OZIPR) model was used to reveal the impact of O₃ precursors on O₃ formation, and 4 base-cases were selected to adjust the model simulation. An average disparity of 18.20% was achieved between the simulated and observed O₃ concentrations. The O₃ isopleth diagram illustrated that O₃ formation in July 2016 was in VOC-sensitive regime, although the VOC/NO_x ratio was greater than 20. By introducing sensitivity (S), a sensitivity analysis was performed for O₃ formation. We found that O₃ formation was sensitive to propylene, (m+p)-xylene, o-xylene and toluene. The results provide theoretical support for O₃ pollution treatment in Shanghai.     

Simulated reaction of formaldehyde and ambient atmospheric particulate matter using a chamber

The reaction of HCHO with Beijing winter's real ambient particulate matter(PM) inside a 3.3 m~3 Teflon Chamber was conducted in this study. NO_2, O_3 and H_2O gases were removed from the ambient aerosol before entering into the chamber. The decays of HCHO were monitored(acetylacetone spectrophotometry method) during the reactions at different PM number concentrations(N_a) and relative humidities(RHs), and the formed particulate formate was detected by IC and XPS techniques. The results showed that when RH was10%–15%, the decay rate of HCHO in the chamber was higher with the existence of PM from relatively clean days(with number concentration(N_a) 200,000 particle/L, 0.35–22.5 μm)compared to dirty days(N_a 200,000 particle/L, 0.35–22.5 μm). When RH increased to 30%–45%, PM can hardly have significant influences on the decay of HCHO. The formations of formate on the reacted PM were consistent with the HCHO decay rates at different ambient PM N_aand RH conditions. This is a first study related to the "real" ambient PM reacted with HCHO and suggested that in the clean and low RH days, PM could be an effective medium for the conversion of HCHO to formate.