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Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

机译:阿拉斯加巴罗市臭氧消耗过程中溴,氯和碘光化学的相互作用

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The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs) has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there have been indications of active iodine chemistry through observed enhancements in filterable iodide, probable detection of tropospheric IO, and recently, observation of snowpack photochemical production of I-2. Despite decades of research, significant uncertainty remains regarding the chemical mechanisms associated with the bromine-catalyzed depletion of ozone, as well as the complex interactions that occur in the polar boundary layer due to halogen chemistry. To investigate this, we developed a zero-dimensional photochemical model, constrained with measurements from the 2009 OA-SIS field campaign in Barrow, Alaska. We simulated a 7-day period during late March that included a full ozone depletion event lasting 3 days and subsequent ozone recovery to study the interactions of halogen radicals under these different conditions. In addition, the effects of iodine added to our Base Model were investigated. While bromine atoms were primarily responsible for ODEs, chlorine and iodine were found to enhance the depletion rates and iodine was found to be more efficient per atom at depleting ozone than Br. The interaction between chlorine and bromine is complex, as the presence of chlorine can increase the recycling and production of Br atoms, while also increasing reactive bromine sinks under certain conditions. Chlorine chemistry was also found to have significant impacts on both HO2 and RO2, with organic compounds serving as the primary reaction partner for Cl atoms. The results of this work highlight the need for future studies on the production mechanisms of Br-2 and Cl-2, as well as on the potential impact of iodine in the High Arctic.
机译:众所周知,北极对流层臭氧的春季耗竭是由雪,冰或气溶胶表面散发出的卤素原子前体引起的活性卤素光化学作用引起的。溴在驱动臭氧消耗事件(ODE)中的作用已被普遍接受,但对于氯自由基在臭氧消耗化学中的作用知之甚少。尽管碘在高北极地区的潜在影响尚不确定,但通过观察到可过滤碘的增强,对流层IO的可能检测以及最近观察到的I-2雪堆光化学产生,已有迹象表明了碘的活跃化学作用。尽管进行了数十年的研究,但是与溴催化的臭氧消耗相关的化学机理以及由于卤素化学作用而在极性边界层中发生的复杂相互作用仍然存在很大的不确定性。为了对此进行调查,我们开发了一个零维光化学模型,并在阿拉斯加巴罗的2009 OA-SIS野战活动中进行了测量。我们模拟了3月下旬的7天时间,其中包括持续3天的完整臭氧消耗事件以及随后的臭氧恢复,以研究在这些不同条件下卤素自由基的相互作用。此外,还研究了将碘添加到我们的基本模型中的影响。虽然溴原子是ODE的主要来源,但发现氯和碘会提高消耗速率,并且发现每个原子上的碘消耗效率比Br高。氯与溴之间的相互作用很复杂,因为氯的存在可以增加Br原子的再循环和产生,同时在某些条件下还可以增加反应性溴的吸收。还发现氯化学对HO2和RO2都有重要影响,其中有机化合物是Cl原子的主要反应伙伴。这项工作的结果表明,有必要进一步研究Br-2和Cl-2的产生机理,以及对高北极地区碘的潜在影响。

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