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Role of dust alkalinity in acid mobilization of iron

机译:粉尘碱度在铁酸迁移中的作用

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pstrongAbstract./strong Atmospheric processing of mineral aerosols by acid gases (e.g., SOsub2/sub, HNOsub3/sub, Nsub2/subOsub5/sub, and HCl) may play a key role in the transformation of insoluble iron (Fe in the oxidized or ferric (III) form) to soluble forms (e.g., Fe(II), inorganic soluble species of Fe(III), and organic complexes of iron). On the other hand, mineral dust particles have a potential of neutralizing the acidic species due to the alkaline buffer ability of carbonate minerals (e.g., CaCOsub3/sub and MgCOsub3/sub). Here we demonstrate the impact of dust alkalinity on the acid mobilization of iron in a three-dimensional aerosol chemistry transport model that includes a mineral dissolution scheme. In our model simulations, most of the alkaline dust minerals cannot be entirely consumed by inorganic acids during the transport across the North Pacific Ocean. As a result, the inclusion of alkaline compounds in aqueous chemistry substantially limits the iron dissolution during the long-range transport to the North Pacific Ocean only a small fraction of iron (&0.2%) dissolves from hematite in the coarse-mode dust aerosols with 0.45% soluble iron initially. On the other hand, a significant fraction of iron (1a??2%) dissolves in the fine-mode dust aerosols due to the acid mobilization of the iron-containing minerals externally mixed with carbonate minerals. Consequently, the model quantitatively reproduces higher iron solubility in smaller particles as suggested by measurements over the Pacific Ocean. It implies that the buffering effect of alkaline content in dust aerosols might help to explain the inverse relationship between aerosol iron solubility and particle size. We also demonstrate that the iron solubility is sensitive to the chemical specification of iron-containing minerals in dust. Compared with the dust sources, soluble iron from combustion sources contributes to a relatively marginal effect for deposition of soluble iron over the North Pacific Ocean during springtime. Our results suggest that more comprehensive data for chemical specificity of iron-rich dust is needed to improve the predictive capability for size-segregated soluble iron particles./p.
机译:> >摘要。酸性气体(例如SO 2 ,HNO 3 ,N 2 sub> O 5 和HCl)可能在不溶性铁(氧化或铁(III)形式的铁)向可溶性形式(例如Fe(II),无机Fe(III)的可溶物质和铁的有机络合物。另一方面,由于碳酸盐矿物(例如,CaCO 3 和MgCO 3 )的碱性缓冲能力,矿物粉尘颗粒具有中和酸性物质的潜力。在这里,我们展示了尘土碱度对包括矿物溶解方案在内的三维气溶胶化学迁移模型中铁酸迁移的影响。在我们的模型模拟中,在穿越北太平洋的过程中,大多数碱性粉尘矿物不能完全被无机酸消耗。结果,在水溶液化学中包含碱性化合物大大限制了铁在远距离运输到北太平洋期间的溶解,只有一小部分铁(<0.2%)从赤铁矿中溶解在粗模式粉尘气溶胶中。最初含0.45%的铁。另一方面,由于外部混合有碳酸盐矿物的含铁矿物的酸动,很大一部分铁(1a-2%)溶解在精细模式的粉尘气溶胶中。因此,该模型定量地重现了较小颗粒中较高的铁溶解度,如在太平洋上进行的测量所暗示的。这暗示粉尘气溶胶中碱含量的缓冲作用可能有助于解释气溶胶铁的溶解度与粒径之间的反比关系。我们还证明了铁的溶解度对粉尘中含铁矿物的化学规格很敏感。与粉尘源相比,来自燃烧源的可溶性铁在春季对北太平洋上的可溶性铁沉积的贡献相对较小。我们的研究结果表明,要提高对尺寸分离的可溶性铁颗粒的预测能力,还需要更全面的富铁粉尘化学特异性数据。

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