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61.
为估算重庆市夏秋季VOCs(挥发性有机物)对O3和SOA(二次有机气溶胶)的生成潜势,利用在线GC-MS/FID在2015年8月22日-9月23日对重庆市区点和郊区点VOCs开展了为期一个月的实时观测,获得市区点和郊区点$ \varphi $(TVOCs)(总挥发性有机物)分别为41.35×10-9和22.72×10-9,其中市区点以烷烃(35.2%)和烯炔烃(25.2%)为主,郊区点以含氧挥发性有机物(oxygenated volatile organic compounds,OVOCs)(30.6%)和烷烃(26.0%)为主.结合最大增量反应活性量化市区点和郊区点VOCs的OFPs(臭氧生成潜势)分别为149.11×10-9和71.09×10-9,市区点OFPs最大的是乙烯、丙烯、甲苯、C8和C9的芳香烃等,郊区点OFPs最大的VOCs是丙烯醛、异戊二烯和甲基乙烯基酮.结合气溶胶生成系数量化郊区点和市区点VOCs对SOA的生成贡献分别为0.36和1.26 μg/m3,相比国内其余城市VOCs的SOAP(二次有机气溶胶生成潜势)较小,主要以甲基环己烷、正壬烷、正葵烷和十一烷等高碳烷烃,以及甲苯、苯、二甲苯和乙苯等芳香烃的SOAP为主.研究显示,控制烯炔烃和芳香烃的浓度有助于控制重庆市O3的生成,控制高碳烷烃和芳香烃则有助于控制重庆市SOA的生成. 相似文献
62.
对西安市各类VOCs人为源进行系统分类,收集活动水平数据,应用国内外排放因子研究的最新成果,采用排放因子法建立了西安市2014年人为源VOCs排放清单.结果表明:2014年西安市人为源大气VOCs排放量为11.51×104t,其中,固定燃烧源、生物质燃烧源、工艺过程源、有机溶剂使用源、移动源、油品存储与销售源和废弃物处理源的排放量分别占VOCs排放总量的2.53%、3.32%、13.30%、51.50%、23.64%、4.82%和1.02%.油墨印刷、建筑涂料和汽车喷涂为有机溶剂使用源重点排放行业,VOCs排放量占到排放总量的48.89%;工艺过程源中化学药品、医药制造、原油加工和化学纤维为重点排放行业,VOCs排放量占到排放总量的10.19%.各区县中,长安区、雁塔区、未央区、碑林区VOCs排放量明显较高,其分担率分别为16.53%、14.88%、14.47%和12.99%. 相似文献
63.
传统北京烤鸭烤制过程中大气污染物的排放特征 总被引:6,自引:5,他引:1
烤鸭是具有北京特色的传统美食之一,制作过程采用果木炭火烤制方式,与其它食物烹饪过程存在明显的差异,国内还未对这类餐饮源的排放特征进行过系统研究,为掌握这类餐饮源排放特征,从而为污染控制提供技术依据,选取北京市具有代表性的烤鸭店,研究了其烤鸭烤制过程中大气污染物的排放特征.结果表明,传统烤鸭烤制过程中排放的油烟、颗粒物、挥发性有机物(VOCs)和醛酮类化合物的基准排放浓度分别为(0.74±0.45)、(15.32±7.93)、(7.60±3.41)和(1.22±0.59)mg·m~(-3);颗粒物排放浓度要远高于油烟排放浓度,VOCs组分构成相对复杂,既包括烷烃、烯烃、芳香烃等VOCs也包括醛酮类、醇类、酯类等含氧VOCs和卤代烃,其中3-甲基呋喃、乙醇和乙酸甲酯的浓度最高;醛酮类化合物的主要组分有乙醛、甲醛和丙烯醛等,其中C1~C3物质占72.27%. 相似文献
64.
北京市典型餐饮企业油烟中醛酮类化合物污染特征 总被引:16,自引:8,他引:8
醛酮类化合物作为餐饮油烟的组成物质之一,是挥发性有机物(volatile organic compounds,VOCs)中化学反应活性较强的一类物质.但目前国内还没有针对餐饮源醛酮类化合物的排放特征进行较为系统的研究.为进一步明确餐饮源醛酮类化合物排放水平和控制现状,获取城市群餐饮源VOCs排放控制决策依据,本研究选取北京市8家不同类型的餐饮企业,采用涂布2,4-二硝基苯肼(DNPH)的硅胶采样管进行油烟样品采集,用超高效液相色谱(UPLC)对油烟样品中的醛酮类化合物进行测定.结果表明按基准风量折算后,8家餐饮企业排放的油烟中醛酮类化合物浓度高低依次是:烤鸭中式烧烤家常菜西式快餐学校食堂中式快餐川菜淮扬菜.餐饮企业油烟中醛酮类化合物(C1~C9)浓度水平范围为115.47~1 035.99μg·m-3.不同类型餐饮企业油烟中醛酮类化合物组分构成存在较为明显的差异,中式餐饮企业醛酮类化合物C1~C3物质所占比例均在40%以上.快餐类餐饮企业醛酮类化合物C4~C9所占比例明显高于其他类型餐饮企业.从醛酮类化合物控制现状来看,北京市目前主流高压静电式油烟净化器对醛酮类化合物的去除效果十分有限. 相似文献
65.
通过批量吸附实验考查了7种芳香族化合物在XAD-4上的吸附热力学行为.结果表明,在实验条件下,Freundlich方程能很好地拟合这7种化合物在XAD-4上的等温吸附数据,且都为优惠吸附,吸附能力均随着温度的升高而降低.结合7种化合物的分子结构描述符和Freundlich方程的吸附平衡常数,建立了QSPR模型,较高的可决系数R2(0.991)、去一法交互检验可决系数R2CV(0.985)和外部预测集交互检验系数Q2ext(0.994)表明,该模型具有较高的稳定性能和预测能力.模型结果表明,水杨酸等7种芳香族化合物在XAD-4上的Freundlich吸附平衡常数与溶质疏水性能呈正比关系,与温度、溶质分子极性和溶质分子的氢键酸度常数呈反比关系. 相似文献
66.
Carbonyl compounds are important intermediates in atmospheric photochemistry, but their primary sources are still not understood well. In this work, carbonyls, hydrocarbons, and alkyl nitrates were continuously measured during November 2011 at a rural site in the Yangtze River Delta region of China. Mixing ratios of carbonyls and hydrocarbons showed large fluctuations during the entire measurement. The average level for total measured volatile organic compounds during the pollution episode from 25th to 27th November, 2011 was 91.6 ppb, about 7 times the value for the clean period of 7th-8th, November, 2011. To preliminarily identify toluene sources at this site, the emission ratio of toluene to benzene (T/B) during the pollution episode was determined based on photochemical ages derived from the relationship of alkyl nitrates to their parent alkanes. The calculated T/B was 5.8 ppb/ppb, significantly higher than the values of 0.2-1.7 ppb/ppb for vehicular exhaust and other combustion sources, indicating the dominant influence of industrial emissions on ambient toluene. The contributions of industrial sources to ambient carbonyls were then calculated using a multiple linear regression fit model that used toluene and alkyl nitrates as respective tracers for industrial emission and secondary production. During the pollution episode, 18.5%, 69.0%, and 52.9% of measured formaldehyde, acetaldehyde, and acetone were considered to be attributable to industrial emissions. The emission ratios relative to toluene for formaldehyde, acetaldehyde, and acetone were determined to be 0.10, 0.20 and 0.40 ppb/ppb, respectively. More research on industrial carbonyl emission characteristics is needed to understand carbonyl sources better. 相似文献
67.
68.
High-surface-area mesoprous powders of γ-Al2O3 doped with Cu2 +, Cr3 +, and V3 + ions were prepared via a modified sol–gel method and were investigated as catalysts for the oxidation of chlorinated organic compounds. The composites retained high surface areas and pore volumes comparable with those of undoped γ-Al2O3 and the presence of the transition metal ions enhanced their surface acidic properties. The catalytic activity of the prepared catalysts in the oxidation of 1,2-dichloroethane (DCE) was studied in the temperature range of 250–400°C. The catalytic activity and product selectivity were strongly dependent on the presence and the type of dopant ion. While Cu2 +- and Cr3 +-containing catalysts showed 100% conversion at 300°C and 350°C, V3 +-containing catalyst showed considerably lower conversion. Furthermore, while the major products of the reactions over γ-alumina were vinyl chloride (C2H3Cl) and hydrogen chloride (HCl) at all temperatures, Cu- and Cr-doped catalysts showed significantly stronger capability for deep oxidation to CO2. 相似文献
69.
Sarah A. Styler 《环境科学学报(英文版)》2015,27(4):132-134
<正>In their recent Journal of Environmental Sciences publication,Wang and colleagues provide field evidence that industrial activities can contribute substantially to atmospheric carbonyl concentrations(Wang et al.,2015).These results may helpto explain underestimations of carbonyl emissions in currently available emission inventories,and highlight the need for an improved understanding of industrial sources of this class of compounds.In the atmosphere,carbonyl compounds photolyze to yield 相似文献
70.
Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H2-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the CeO2 fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species. 相似文献