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Global modeling of nitrate and ammonium aerosol: Radiative effect and interaction with gas-phase chemistry and aerosols.

机译:硝酸盐和铵盐气溶胶的整体模型:辐射效应以及与气相化学物质和气溶胶的相互作用。

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摘要

Nitrate and ammonium aerosols are included in a global model. First, in order to examine the potential importance of sea salt and mineral dust aerosol on radiative effects by nitrate and ammonium, we used a thermodynamic equilibrium model to calculate aerosol composition, including nitrate and ammonium in aerosol, and water content. This equilibrium study finds that the presence of sea salt and dust aerosol could potentially increase nitrate aerosol burden by a factor of 4. As a result, global and annual average forcing by anthropogenic aerosols decreases by 12%, from -0.42 to -0.37 Wm-2 for the present day and from -0.54 to -0.47 Wm-2 for an IPCC projected emission scenario for 2100, respectively.; Then, a more accurate hybrid dynamical approach is developed for use in the global chemistry-aerosol transport model to simulate nitrate and ammonium aerosols. In this study, gas-to-particle mass transport limitations are considered in partitioning of nitrate and ammonium between gas and aerosol phases. Simulated nitrate and ammonium aerosol concentrations are generally within a factor of 2 of observations. The global burden of nitrate and ammonium is 0.165 and 0.225 Tg N, with a lifetime of 4.85 and 3.41 days, respectively. 48% of nitrate and 90% of ammonium exist in the optically important size range. Nitrate formation could potentially decrease tropospheric ozone due to the decrease of NO x.; Several sensitivity studies were performed to analyze differences in nitrate and ammonium aerosol concentrations, between simplified methods (including the equilibrium model) for treating nitrate and ammonium in aerosol and the method developed here. It is indicated that these simplifications may result in an over-estimate of the reduction of tropospheric ozone and an overestimate of nitrate aerosol forcing, because they significantly overpredict the nitrate uptake by aerosols, especially that by dust aerosol.; Finally, nitrate aerosol concentration is sensitive to the vertical representations of clouds in global models, since clouds have a large impact on the photo dissociation of its gaseous precursor, HNO3, through interference with ultra-violet solar radiation. The effects of cloud overlap schemes on photolysis frequencies and tropospheric OH concentrations are thus examined in a global photochemistry model.
机译:全局模型中包括硝酸盐和铵气雾剂。首先,为了检查海盐和矿物粉尘气溶胶对硝酸盐和铵盐的辐射作用的潜在重要性,我们使用热力学平衡模型来计算气溶胶成分,包括气溶胶中的硝酸盐和铵盐以及水含量。这项平衡研究发现,海盐和粉尘气溶胶的存在可能使硝酸盐气溶胶负担增加4倍。结果,人为气溶胶的全球和年度平均强迫降低了12%,从-0.42降至-0.37 Wm- IPCC的预计排放情景为2;目前为2; IPCC的预计排放情景为-0.54至-0.47 Wm-2;然后,开发了一种更精确的混合动力方法,用于全球化学-气溶胶传输模型,以模拟硝酸盐和铵气溶胶。在这项研究中,在气相和气溶胶相之间分配硝酸盐和铵盐时,考虑了气体到颗粒的传质限制。模拟的硝酸盐和铵气溶胶浓度通常在观测值的2倍以内。硝酸盐和铵的全球负荷为0.165 Tg N和0.225 Tg N,寿命分别为4.85天和3.41天。在光学上重要的尺寸范围内存在48%的硝酸盐和90%的铵。由于NO x的减少,硝酸盐的形成有可能减少对流层臭氧。在简化方法(包括平衡模型)和气溶胶中硝酸盐和铵的处理方法之间进行了一些敏感性研究,以分析硝酸盐和铵气溶胶浓度的差异。结果表明,这些简化可能导致对流层臭氧减少的高估和硝酸盐气溶胶强迫的高估,因为它们大大高估了气溶胶,尤其是粉尘气溶胶对硝酸盐的吸收。最后,硝酸盐气溶胶浓度对全局模型中云的垂直表示很敏感,因为云通过干扰紫外线太阳辐射对其气态前体HNO3的光解有很大影响。因此,在全球光化学模型中研究了云重叠方案对光解频率和对流层OH浓度的影响。

著录项

  • 作者

    Feng, Yan.;

  • 作者单位

    University of Michigan.;

  • 授予单位 University of Michigan.;
  • 学科 Physics Atmospheric Science.; Environmental Sciences.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 265 p.
  • 总页数 265
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 大气科学(气象学);环境科学基础理论;
  • 关键词

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