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Understanding the primary emissions and secondary formation of gaseous organic acids in the oil sands region of Alberta, Canada

机译:了解加拿大艾伯塔省油砂区气体有机酸的主要排放和二次形成

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Organic acids are known to be emitted from combustion processes and are key photochemical products of biogenic and anthropogenic precursors. Despite their multiple environmental impacts, such as on acid deposition and human–ecosystem health, little is known regarding their emission magnitudes or detailed chemical formation mechanisms. In the current work, airborne measurements of 18 gas-phase low-molecular-weight organic acids were made in the summer of 2013 over the oil sands region of Alberta, Canada, an area of intense unconventional oil extraction. The data from these measurements were used in conjunction with emission retrieval algorithms to derive the total and speciated primary organic acid emission rates, as well as secondary formation rates downwind of oil sands operations. The results of the analysis indicate that approximately 12?t?day?1 of low-molecular-weight organic acids, dominated by C1–C5 acids, were emitted directly from off-road diesel vehicles within open pit mines. Although there are no specific reporting requirements for primary organic acids, the measured emissions were similar in magnitude to primary oxygenated hydrocarbon emissions, for which there are reporting thresholds, measured previously (?≈??20?t?day?1). Conversely, photochemical production of gaseous organic acids significantly exceeded the primary sources, with formation rates of up to ?≈??184?t?day?1 downwind of the oil sands facilities. The formation and evolution of organic acids from a Lagrangian flight were modelled with a box model, incorporating a detailed hydrocarbon reaction mechanism extracted from the Master Chemical Mechanism (v3.3). Despite evidence of significant secondary organic acid formation, the explicit chemical box model largely underestimated their formation in the oil sands plumes, accounting for 39, 46, 26, and 23?% of the measured formic, acetic, acrylic, and propionic acids respectively and with little contributions from biogenic VOC precursors. The model results, together with an examination of the carbon mass balance between the organic acids formed and the primary VOCs emitted from oil sands operations, suggest the existence of significant missing secondary sources and precursor emissions related to oil sands and/or an incomplete mechanistic and quantitative understanding of how they are processed in the atmosphere.
机译:已知有机酸从燃烧过程中发射并是生物和人为前体的关键光化学产物。尽管它们的多种环境影响,例如酸沉积和人类生态系统的健康,但对它们的排放量或详细的化学形成机制很少。在目前的工作中,在2013年夏天,在加拿大艾伯塔省的油砂区夏季制造了18个气相低分子量有机酸的空气载量测量。来自这些测量的数据与排放检索算法结合使用,以导出总和所指的初级有机酸排放率,以及油砂操作的二次形成速率。分析结果表明,由C1-C5酸支配的低分子量有机酸中大约12?T?的一天α1,直接从露天坑内内的越野柴油车发射。尽管对原发性有机酸没有特异性报告要求,但是测量的排放的幅度与初级含氧烃排放相似,报告阈值,以前测量,以前测量(?≈Ω·t?日?1)。相反,气态有机酸的光化学生产显着超过了主要来源,形成率达到?≈αn184?t?1下风的油砂设施。从拉格朗日飞行中的有机酸的形成和演化用盒式模型进行了建模,其含有从母系中提取的详细的烃反应机理(V3.3)。尽管有明显的二次有机酸形成的证据,但显式化学盒模型在很大程度上低估了它们在油砂羽毛中形成的形成,分别占测量的甲型,乙型,丙烯酸和丙酸的39,46,26和23倍从生物生物转向前体的贡献很少。模型结果,以及在形成的有机酸之间的碳质量平衡和从油砂作用发出的主要转录的检查,表明存在显着缺失的二级来源和与油砂和/或不完全机制相关的前体排放定量了解它们在大气中如何处理的理解。
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