冬夏季广州城区碳气溶胶特征及其与O_3和气象条件的关联

2008年1月1日～31日和7月1日～31日在广州城区每天采集1个PM2.5样品,对样品进行碳成分分析,得到有机碳(OC)、元素碳(EC)浓度.同步观测了气象因子以及SO2、NO2、O3气态污染物浓度.结果发现,冬季和夏季PM2.5日均值质量浓度分别为(81.2±61.4)μg.m-3和(53.7±23.2)μg.m-3,OC质量浓度分别为(24.6±19.3)μg.m-3和(14.0±5.6)μg.m-3,EC质量浓度分别为(7.9±5.4)μg.m-3和(4.7±2.2)μg.m-3,OC/EC比值分别为2.9±0.6和3.2±1.0.冬夏季非降雨的稳定天气条件下二次有机碳气溶胶(SOC)浓度分别为(6.1±6.6)μg.m-3和(5.8±5.2)μg.m-3.冬夏季SOC和O3浓度显著相关(p0.01).东南风和西南风条件下,OC、EC浓度普遍较高,表明东莞、江门和佛山地区的工业污染源对广州地区污染物累积和霾天气的形成有一定的贡献.     

臭氧技术在城市湖泊水环境修复中的应用——以深圳市荔枝湖治理工程为例

以深圳市荔枝湖为例,通过枯水期历时8个月的水质连续监测,分析臭氧技术在修复城市湖泊水质中的作用及效果。结果表明,监测期间湖水CODMn≤10mg/L,氨氮<0.6mg/L,总磷<0.08mg/L,透明度在60~120cm间,水质满足景观水体要求,表明应用该技术可以取得较好的修复效果。     

Degradation of 17α-ethinylestradiol by ozonation--identification of the by-products and assessment of their estrogenicity and toxicity

The presence of the synthetic estrogen 17α-ethinylestradiol (EE2) in waters at low levels is a concern due to its ability to act as an endocrine disruptor. Ozone (O₃) is commonly used in water treatment and reacts with EE2 to form by-products having characteristics that are mostly unknown. The aim of this study was to identify the by-products of E2 and EE2 ozonation and determine their estrogenicity and toxicity relative to the parent compound. Ozonation by-products were identified via LC-MS analysis. The estrogenicity was measured using the YES assay, and toxicity was determined by monitoring effects on histology of fetal rat testes and testosterone secretion by these tissues. Two EE2 by-products were identified with open phenolic ring structures (masses 302 and 344 u). The Yeast Estrogen Screening (YES) assay showed a decreased but incomplete removal of estrogenicity after ozonation of EE2. Histological analysis of fetal testes revealed that neither E2 nor EE2, with or without ozonation, had any effect on seminiferous cord formation; however, a remarkable negative effect on testosterone secretion was observed, with EE2 by-products after ozonation showing the most rapid and extensive inhibition. These results show that the removal of EE2 via reaction with O₃ resulted in the formation of by-products that are less estrogenic (as demonstrated by the YES assay), but have a greater negative impact on testosterone secretion. Thus, the disappearance of the parent compound is not a sufficient endpoint, as the by-products created may be more toxic. Care should be taken when implementing oxidation applications such as ozone during waste water treatment.     

Characteristics of one-year observation of VOCs, NOx, and O3 at an urban site in Wuhan, China

A continuous online observation of ozone and its precursors(NOx, VOCs) was carried out in central urban Wuhan from September 2016 to August 2017. The concentration levels of ozone,NOx, VOCs and their variations in urban Wuhan were analyzed, as well as effects of VOCs on ozone photochemical generation and the main controlling factors for ozone production. During the observation period, the average concentrations of ozone and NOx in Wuhan was 22.63 and30.14 ppbv, respectively, and the average concentration of VOCs was 32.61 ppbv(42.3% alkanes,13.0% alkenes, 10.0% aromatics, 7.3% acetylene, 9.9% OVOCs, and 10.5% halohydrocarbons).Ozone concentration was higher in spring and summer as compared with autumn and winter,wheras VOCs and NOx concentratios were lower in spring and summer but higher in autumn and winter. Aromatics and alkenes, two of VOCs species, showed the highest contributions to ozone formation potential in Wuhan(35.7% alkenes, 35.4 aromatics, 17.5% alkanes, 8.6% OVOCs,1.6% halogenated hydrocarbons, and 1.4% acetylene). Among all VOCs species, those with the highest contribution were ethylene, m-xylene, toluene, propylene and o-xylene. The contribution of these five compounds to the total ozone formation potential concentration was 43.90%.Ozone-controlling factors in Wuhan changed within one day; during the early morning hours(6:00–9:00), VOCs/NOx was low, and ozone generation followed a VOCs-limited regime.However, during the peak time of ozone concentration(12:00–16:00), the ratio of VOCs/NOx was relatively high, suggesting that ozone generation followed a NOx-limited regime.     

Characterization, reactivity, source apportionment, and potential source areas of ambient volatile organic compounds in a typical tropical city

Based on one-year observation, the concentration, sources, and potential source areas of volatile organic compounds (VOCs) were comprehensively analyzed to investigate the pollution characteristics of ambient VOCs in Haikou, China. The results showed that the annual average concentration of total VOCs (TVOCs) was 11.4 ppbV, and the composition was dominated by alkanes (8.2 ppbV, 71.4%) and alkenes (1.3 ppbV, 20.5%). The diurnal variation in the concentration of dominant VOC species showed a distinct bimodal distribution with peaks in the morning and evening. The greatest contribution to ozone formation potential (OFP) was made by alkenes (51.6%), followed by alkanes (27.2%). The concentrations of VOCs and nitrogen dioxide (NO₂) in spring and summer were low, and it was difficult to generate high ozone (O₃) concentrations through photochemical reactions. The significant increase in O₃ concentrations in autumn and winter was mainly related to the transmission of pollutants from the northeast. Traffic sources (40.1%), industrial sources (19.4%), combustion sources (18.6%), solvent usage sources (15.5%) and plant sources (6.4%) were identified as major sources of VOCs through the positive matrix factorization (PMF) model. The southeastern coastal areas of China were identified as major potential source areas of VOCs through the potential source contribution function (PSCF) and concentration-weighted trajectory (CWT) models. Overall, the concentration of ambient VOCs in Haikou was strongly influenced by traffic sources and long-distance transport, and the control of VOCs emitted from vehicles should be strengthened to reduce the active species of ambient VOCs in Haikou, thereby reducing the generation of O₃.     

Disinfection byproduct formation from algal organic matters after ozonation or ozone combined with activated carbon treatment with subsequent chlorination

Algal organic matter (AOM), including extracellular organic matter (EOM) and intracellular organic matter (IOM) from algal blooms, is widely accepted as essential precursors of disinfection byproducts (DBPs). This study evaluated the effect of ozonation or ozone combined with activated carbon (O₃-AC) treatment on characteristic alternation and DBP formation with subsequent chlorination of Chlorella sp.. The effects of pH and bromide concentration on DBP formation by ozonation or O₃-AC treatment were also investigated. Results showed that the potential formation of DBPs might be attributed to ozonation, but these DBP precursors could be further removed by activated carbon (AC) treatment. Moreover, the formation of target DBPs was controlled at acidic pH by alleviating the reactions between chlorine and AOM. Besides, the bromide substitution factor (BSF) value of trihalomethanes (THMs) from EOM and IOM remained constant after AC treatment. However, THM precursors could be significantly decreased by AC treatment. The above results indicated that O₃-AC was a feasible treatment method for algal-impacted water.     

Characteristics of ozone pollution and the sensitivity to precursors during early summer in central plain, China

In this study, we conducted an observation experiment from May 1 to June 30, 2018 in Zhengzhou, a major city in central China, where ground ozone (O₃) pollution has become serious in recent years. The concentrations of O₃ and its precursors, as well as H₂O₂ and meteorological data were obtained from the urban site (Yanchang, YC), suburban (Zhengzhou University, ZZU) and background sites (Ganglishuiku, GLSK). Result showed that the rates of O₃ concentration exceeded Chinese National Air Quality Standard Grade II (93.3 ppbv) were 59.0%, 52.5%, and 55.7% at the above three sites with good consistency, respectively, indicating that O₃ pollution is a regional problem in Zhengzhou. The daily peak O₃ appeared at 15:00–16:00, which was opposite to VOCs, NO_x, and CO and consistent with H₂O₂. The exhaustive statistical analysis of meteorological factors and chemical effects on O₃ formation at YC was advanced. The high concentration of precursors, high temperature, low relative humidity, and moderately high wind speed together with the wind direction dominated by south and southeast wind contribute to urban O₃ episodes in Zhengzhou. O₃ formation analysis showed that reactive alkenes such as isoprene and cis-2-butene contributed most to O₃ formation. The VOCs/NO_x ratio and smog production model were used to determine O₃-VOC-NO_x sensitivity. The O₃ formation in Zhengzhou during early summer was mainly under VOC-limited and transition regions alternately, which implies that the simultaneous emission reduction of alkenes and NO_x is effective in reducing O₃ pollution in Zhengzhou.     

株洲市臭氧污染状况及相关气象因子分析

采用2013年1～12月空气质量自动监测数据对株洲市臭氧污染现状及相关气象因子进行分析。结果表明:监测期间全年臭氧日最大8 h平均浓度一级标准值达标率达到71.8%,全年超标率为1.6%,超标主要出现在季节变换时期。臭氧日最大8 h平均浓度的月均值变化呈"M"型,浓度高值持续时间长。日变化规律较强,且不同季节变化特征略有差别。臭氧浓度与气温有正相关性,相关系数为0.612;与湿度和云量有负相关性,且臭氧与湿度负相关性较明显,相关系数为0.731。     

Leaf size and surface characteristics of Betula papyrifera exposed to elevated CO2 and O3

Betula papyrifera trees were exposed to elevated concentrations of CO₂ (1.4 × ambient), O₃ (1.2 × ambient) or CO₂ + O₃ at the Aspen Free-air CO₂ Enrichment Experiment. The treatment effects on leaf surface characteristics were studied after nine years of tree exposure. CO₂ and O₃ increased epidermal cell size and reduced epidermal cell density but leaf size was not altered. Stomatal density remained unaffected, but stomatal index increased under elevated CO₂. Cuticular ridges and epicuticular wax crystallites were less evident under CO₂ and CO₂ + O₃. The increase in amorphous deposits, particularly under CO₂ + O_3, was associated with the appearance of elongated plate crystallites in stomatal chambers. Increased proportions of alkyl esters resulted from increased esterification of fatty acids and alcohols under elevated CO₂ + O₃. The combination of elevated CO₂ and O₃ resulted in different responses than expected under exposure to CO₂ or O₃ alone.