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51.
Chengdu is a megacity in the southwest of China with high ozone (O3) mixing ratio. Observation of volatile organic compounds (VOCs), NO2 and O3 with high temporal resolution was conducted in Chengdu to investigate the chemical processes and causes of high O3 levels. The hourly mixing ratios of VOCs, NO2, and O3 were monitored by an online system from 28 August to 7 October, 2016. According to meteorological conditions, Chengdu, with relative warm weather and low wind speed, is favorable to O3 formation. Part of the O3 in Chengdu may be transported from the downtown area. In O3 episodes, the average mixing ratios of NO2 and O3 were 20.20?ppbv and 47.95?ppbv, respectively. In non-O3 episodes, the average mixing ratios of NO2 and O3 were 16.38?ppbv and 35.15?ppbv, respectively. The average mixing ratio of total VOCs (TVOCs) was 40.29?ppbv in non-O3 episodes, which was lower than that in O3 episodes (53.19?ppbv). Alkenes comprised 51.7% of the total O3 formation potential (OFP) in Chengdu, followed by aromatics which accounted for 24.2%. Ethylene, trans-pentene, propene, and BTEX (benzene, ethylbenzene, toluene, m/p-xylene, o-xylene) were also major contributors to the OFP in Chengdu. In O3 episodes, intensive secondary formations were observed during the campaign. Oxygenated VOCs (OVOCs), such as acetone, Methylethylketone (MEK), and Methylvinylketone (MVK) were abundant. Isoprene rapidly converted to MVK and Methacrolein (MACR) during O3 episodes. Acetone was mainly the oxidant of C3-C5 hydrocarbons. 相似文献
52.
Da Sheng Lingjun Bu Shumin Zhu Yangtao Wu Jue Wang Nan Li Shiqing Zhou 《环境科学学报(英文版)》2022,34(7):21-27
Pre-oxidation has been reported to be an effective way to remove algal cells in water, but the released algal organic matter (AOM) could be oxidized and lead to the increment in disinfection by-product (DBP) formation. The relationship between pre-oxidation and AOM-derived DBP formation needs to be approached more precisely. This study compared the impact of four pre-oxidants, ozone (O3), chlorine dioxide (ClO2), potassium permanganate (KMnO4) and sodium hypochlorite (NaClO), on the formation of nitrogenous (N-) and carbonaceous (C-) DBPs in AOM chlorination. The characterization (fluorescent properties, molecular weight distribution and amino acids concentration) on AOM samples showed that the characterization properties variations after pre-oxidation were highly dependent on the oxidizing ability of oxidants. The disinfection experiments showed that O3 increased DBP formation most significantly, which was consistent with the result of characterization properties variations. Then canonical correspondent analysis (CCA) and Pearson's correlation analysis were conducted based on the characterization data and DBP formation. CCA indicated that C-DBPs formation was highly dependent on fluorescent data. The formation of haloacetic acids (HAAs) had a positive correlation with aromatic protein-like component while trichloromethane (TCM) had a positive correlation with fulvic acid-like component. Pearson's correlation analysis showed that low molecular weight fractions were favorable to form N-DBPs. Therefore, characterization data could provide the advantages in the control of DBP formation, which further revealed that KMnO4 and ClO2 were better options for removing algal cells as well as limiting DBP formation. 相似文献
53.
源水水质的恶化给传统的饮用水处理工艺带来了挑战.生物过滤是饮用水消毒输配之前管理、维护及增强颗粒滤料表面生物活性以去除有机和无机物的过程.由于具有高效、低成本等优点,生物过滤在饮用水深度处理工艺中逐渐得到广泛的应用.本文综述了生物过滤在饮用水处理过程中对水中溶解性有机质(消毒副产物前体物)的去除、微量污染物的削减、嗅味化合物及氨氮的去除等.此外,针对生物过滤在水深度处理过程中存在的问题,本文详细讨论了含氮消毒副产物前体物的生成、低温下生物过滤效能下降等挑战,并提出了今后需要研究的问题. 相似文献
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杭州湾北岸上海段石化集中区臭氧重污染过程研究 总被引:1,自引:0,他引:1
为研究杭州湾O3污染的形成机制,采用在线监测系统对杭州湾北岸上海段石化集中区O3及其前体物开展了为期1个月(2019年5月)的同步连续观测.采用OZIPR(臭氧等值线研究)模型分析O3生成的敏感性.在O3重度污染期间,利用PMF(正定矩阵因子分解)模型对O3前体物——VOCs进行源解析,采用臭氧生成潜势及气团老化分别估算了VOCs的反应活性和化学消耗.结果表明:①2019年5月杭州湾北岸上海段石化集中区O3的IAQI(空气质量分指数)优良率仅为61.3%,ρ(O3)第90%分位值为173.0 μg/m3.5月22日、23日发生重度O3污染,O3日最大8 h滑动平均值分别为(284.4±19.2)(282.0±14.2)μg/m3,分别超过GB 3095—2012《环境空气质量标准》二级标准限值(160 μg/m3)的77.75%和76.25%.②O3的生成受VOCs控制,降低VOCs的排放可在一定程度上降低O3的生成,降低NOx的排放反而会促进O3的生成.③O3重度污染期间,VOCs主要来自化工区排放(72.35%)和机动车尾气排放(27.65%).④O3重度污染期间,烯烃、炔烃及芳香烃对O3生成的贡献率之和在80.00%以上,其中丙烯、乙烯和甲苯的贡献率分别为29.97%、15.60%和14.16%;芳香烃及烯烃和炔烃是最主要的VOCs化学消耗物种,其中φ(丙烯)、φ(乙烯)和φ(1,2,4-三甲苯)的消耗量分别为13.57×10-9、4.93×10-9和3.55×10-9.研究显示,杭州湾北岸上海段5月O3的生成受化工区影响显著,丙烯与乙烯是O3重污染期间关键的O3前体物. 相似文献
56.
57.
This study was designed to clarify the influence of operating conditions on the formation and emissions of polychlorinated-pdibenzodioxins and dibenzofurans (PCDD/Fs) from a sintering process with hot flue gas recycling. A pilot scale sinter pot with simulated flue gas recycling was developed, and four key operational parameters, including temperature, oxygen content of the simulated waste flue gas, the coke rate of the sintering mixture, and the quicklime quality, were selected for exploring PCDD/Fs formation. The results showed that the temperature of the recycled flue gas had a major affect on PCDD/Fs formation, and a high temperature could significantly increase their formation during sintering. A clear linear correlation between the temperature of recycling flue gas and PCDD/Fs emission (r = 0.93) was found. PCDD/Fs could be reduced to a certain extent by decreasing the level of oxygen in the recycled flue gas, while sintering quality was unchanged. The coke rate had no significant influence on the formation of PCDD/Fs, but the quality of quicklime used in the sintering mixture could affect not only the amount of PCDD/Fs emissions but also the sintering productivity. Compared with a benchmark sinter pot test, PCDD/Fs emissions markedly decreased with improvements to quicklime quality. However, the reduction in PCDD/Fs emissions realized by using high-quality quicklime was limited by the temperature of the inlet gas. The highest reduction achieved was 51% compared with conventional quicklime when the temperature of the inlet gas was 150°C. 相似文献
58.
在水资源紧缺的当下,污水再生利用是一项重要的环保战略更是资源战略.消毒能有效杀灭病菌和阻断介水疾病的传播,是保障再生水用水安全的重要手段.然而,消毒剂会不可避免地与水中有机物发生反应形成具有毒害效应的消毒副产物.围绕污水在再生消毒过程中所产生的消毒副产物,针对其检测识别方法、生成条件(前体物、消毒工艺及水质条件对消毒副产物生成的影响)以及控制方法(源头控制、过程控制及末端控制)进行综述.在此基础上,对再生水消毒副产物的未来研究动态进行了探讨,可为保障再生水的安全利用提供依据. 相似文献
59.
《Greenhouse Gases: Science and Technology》2018,8(3):402-428
In oxy‐fuel combustion, fuel is burned using oxygen together with recycled flue gas, which is needed to control the combustion temperature. This leads to higher concentrations of sulfur dioxide and sulfur trioxide in the recycled gas, which can result in the formation of sulfuric acid and enhanced corrosion. Current experimental data on SO3 formation, reaction mechanisms, and mathematical modelling have indicated significant differences in SO3 formation between air‐ and oxy‐fuel combustion for both the wet and dry flue gas recycle options. This paper provides an extensive review of sulfur trioxide formation in air‐ and oxy‐fuel combustion environments, with an emphasis on coal‐fired systems. The first part summarizes recent findings on oxy‐fuel combustion experiments, as they affect sulfur trioxide formation. In the second part, the review focuses on sulfur trioxide formation mechanisms, and the influence of catalysis on sulfur trioxide formation. Finally, the current methods for measuring sulfur trioxide concentration are also reviewed along with the major difficulties associated with those measurements using data available from both bench‐ and pilot‐scale units. © 2018 Society of Chemical Industry and John Wiley & Sons, Ltd. 相似文献
60.