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Temperature and volatile organic compound concentrations as controlling factors for chemical composition of α -pinene-derived secondary organic aerosol

机译:温度和挥发性有机化合物浓度作为α-新烯烃衍生的二次有机气溶胶化学成分的控制因子

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This work investigates the individual and combined effects of temperature and volatile organic compound precursor concentrations on the chemical composition of particles formed in the dark ozonolysis of α -pinene. All experiments were conducted in a 5?m 3 Teflon chamber at an initial ozone concentration of 100?ppb and initial α -pinene concentrations of 10 and 50?ppb, respectively; at constant temperatures of 20, 0, or ? 15? ° C; and at changing temperatures (ramps) from ? 15 to 20 and from 20 to ? 15? ° C. The chemical composition of the particles was probed using a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). A four-factor solution of a positive matrix factorization (PMF) analysis of the combined HR-ToF-AMS data is presented. The PMF analysis and the elemental composition analysis of individual experiments show that secondary organic aerosol particles with the highest oxidation level are formed from the lowest initial α -pinene concentration (10?ppb) and at the highest temperature (20? ° C). A higher initial α -pinene concentration (50?ppb) and/or lower temperature (0 or ? 15? ° C) results in a lower oxidation level of the molecules contained in the particles. With respect to the carbon oxidation state, particles formed at 0? ° C are more comparable to particles formed at ? 15? ° C than to those formed at 20? ° C. A remarkable observation is that changes in temperature during particle formation result in only minor changes in the elemental composition of the particles. Thus, the temperature at which aerosol particle formation is induced seems to be a critical parameter for the particle elemental composition. Comparison of the HR-ToF-AMS-derived estimates of the content of organic acids in the particles based on m / z ?44 in the mass spectra show good agreement with results from off-line molecular analysis of particle filter samples collected from the same experiments. Higher temperatures are associated with a decrease in the absolute mass concentrations of organic acids (R-COOH) and organic acid functionalities (-COOH), while the organic acid functionalities account for an increasing fraction of the measured particle mass.
机译:该作品研究了温度和挥发性有机化合物前体浓度对α-烯烃的暗臭臭氧层中形成的颗粒化学成分的个体和综合作用。所有实验均以初始臭氧浓度为100·ppb的臭氧浓度,初始α-丁烯浓度为10和50μppb。在20,0的恒定温度下或? 15? °C;在改变温度(斜坡)时? 15到20和20到? 15? ℃。使用高分辨率飞行时间气溶胶质谱仪(HR-TOF-AMS)探测颗粒的化学成分。介绍了对HR-TOF-AMS数据的正矩阵分解(PMF)分析的四因素溶液。单个实验的PMF分析和元素组成分析表明,具有最高氧化水平的二次有机气溶胶颗粒由最低初始α-烯烃浓度(10→PPB)和最高温度(20Ω·℃)形成。初始α-一烯烯浓度(50〜ppb)和/或更低的温度(0或α15Ω·c)导致颗粒中含有的分子的较低氧化水平。关于碳氧化态,在0时形成的颗粒? °C与形成颗粒更媲美? 15? °C比在20个形成的那些? ℃。显着的观察是颗粒形成期间的温度变化导致颗粒的元素组成的微小变化。因此,诱导气溶胶颗粒形成的温度似乎是颗粒元素组合物的关键参数。基于M / Zβ44的颗粒中有机酸含量的HR-TOF-AMS衍生估计的比较显示出良好的一致性与从相同收集的颗粒过滤器样品的离线分子分析结果实验。较高的温度与有机酸(R-COOH)和有机酸官能团(-COOH)的绝对质量浓度的减少相关,而有机酸官能团占测量颗粒质量的增加。

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