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首页> 外文期刊>Atmospheric chemistry and physics >Atmospheric organic matter in clouds: exact masses and molecular formula identification using ultrahigh-resolution FT-ICR mass spectrometry
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Atmospheric organic matter in clouds: exact masses and molecular formula identification using ultrahigh-resolution FT-ICR mass spectrometry

机译:云中的大气有机物:使用超高分辨率FT-ICR质谱仪进行精确质量和分子式鉴定

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Clouds alter the composition of atmospheric aerosol by acting as a medium for interactions between gasand particulate-phase substances. To determine the cloud water atmospheric organic matter (AOM) composition and study the cloud processing of aerosols, two samples of supercooled clouds were collected at the Storm Peak Laboratory near Steamboat Springs, Colorado (3220ma.s.l.). Approximately 3000 molecular formulas were assigned to ultrahighresolution mass spectra of the samples after using a reversedphase extraction procedure to isolate the AOM components from the cloud water. Nitrogen-containing compounds (CHNO compounds), sulfur-containing compounds (CHOS and CHNOS compounds) and other oxygen-containing compounds (CHO compounds) with molecular weights up to 700 Da were observed. Average oxygen-to-carbon ratios of ~0.6 indicate a slightly more oxidized composition than most water-soluble organic carbon identified in aerosol studies, which may result from aqueous oxidation in the clouds. The AOM composition indicates significant influences from biogenic secondary organic aerosol (SOA) and residential wood combustion. We observed 60% of the cloud water CHO molecular formulas to be identical to SOA samples of β-pinene, β-pinene, d-limonene, and β-caryophyllene ozonolysis. CHNO compounds had the highest number frequency and relative abundances and are associated with residential wood combustion and NO_x oxidation. Multiple nitrogen atoms in the assigned molecular formulas for the nighttime cloud sample composite were observed, indicating the significance of nitrate radical reactions on the AOM composition. Several CHOS and CHNOS compounds with reduced sulfur (in addition to the commonly observed oxidized sulfur-containing compounds) were also observed; however further investigation is needed to determine the origin of the reduced sulfur-containing compounds. Overall, the molecular composition determined using ultrahighresolution Fourier-transform ion cyclotron resonance (FTICR) mass spectrometry provides an unambiguous identification of the cloud water organic anion composition in the Rocky Mountain area that could help to improve the understanding of aqueous-phase processes.
机译:云通过充当气体与颗粒相物质之间相互作用的媒介来改变大气气溶胶的组成。为了确定云水中的大气有机质(AOM)组成并研究气溶胶的云处理,在科罗拉多州Steamboat Springs附近的Storm Peak实验室(3220ma.s.l。)收集了两个过冷云样品。在使用反相萃取程序从云水中分离出AOM组分后,将大约3000个分子式分配给了样品的超高分辨率质谱。观察到分子量最高为700 Da的含氮化合物(CHNO化合物),含硫化合物(CHOS和CHNOS化合物)和其他含氧化合物(CHO化合物)。约0.6的平均氧碳比表明,与大多数气溶胶研究中确定的大多数水溶性有机碳相比,其氧化成分略多,这可能是由于云层中的水氧化所致。 AOM成分表明受到生物二次有机气溶胶(SOA)和住宅木材燃烧的重大影响。我们观察到60%的云水CHO分子式与β-pine烯,β-pine烯,d-柠檬烯和β-石竹烯臭氧分解的SOA样品相同。 CHNO化合物具有最高的频率和相对丰度,并且与住宅木材燃烧和NO_x氧化有关。观察到夜间云样品复合材料的指定分子式中有多个氮原子,表明硝酸根自由基反应对AOM组成具有重要意义。还观察到了几种具有减少的硫的CHOS和CHNOS化合物(除了通常观察到的氧化的含硫化合物)。然而,需要进一步研究以确定还原的含硫化合物的来源。总体而言,使用超高分辨率傅里叶变换离子回旋共振(FTICR)质谱法测定的分子组成可对洛矶山脉地区的云水有机阴离子组成进行明确鉴定,从而有助于增进对水相过程的了解。

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