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在不同的实验室条件下形成硫酸盐和元素硫气溶胶:对早期地球的影响。

The formation of sulfate and elemental sulfur aerosols under varying laboratory conditions: implications for early earth.

机构信息

Department of Chemistry and Biochemistry, University of Colorado at Boulder, Boulder, Colorado 80309, USA.

出版信息

Astrobiology. 2010 Oct;10(8):773-81. doi: 10.1089/ast.2009.9455.

DOI:10.1089/ast.2009.9455
PMID:21087157
Abstract

The presence of sulfur mass-independent fractionation (S-MIF) in sediments more than 2.45 × 10(9) years old is thought to be evidence for an early anoxic atmosphere. Photolysis of sulfur dioxide (SO(2)) by UV light with λ < 220 nm has been shown in models and some initial laboratory studies to create a S-MIF; however, sulfur must leave the atmosphere in at least two chemically different forms to preserve any S-MIF signature. Two commonly cited examples of chemically different sulfur species that could have exited the atmosphere are elemental sulfur (S(8)) and sulfuric acid (H(2)SO(4)) aerosols. Here, we use real-time aerosol mass spectrometry to directly detect the sulfur-containing aerosols formed when SO(2) either photolyzes at wavelengths from 115 to 400 nm, to simulate the UV solar spectrum, or interacts with high-energy electrons, to simulate lightning. We found that sulfur-containing aerosols form under all laboratory conditions. Further, the addition of a reducing gas, in our experiments hydrogen (H(2)) or methane (CH(4)), increased the formation of S(8). With UV photolysis, formation of S(8) aerosols is highly dependent on the initial SO(2) pressure; and S(8) is only formed at a 2% SO(2) mixing ratio and greater in the absence of a reductant, and at a 0.2% SO(2) mixing ratio and greater in the presence of 1000 ppmv CH(4). We also found that organosulfur compounds are formed from the photolysis of CH(4) and moderate amounts of SO(2). The implications for sulfur aerosols on early Earth are discussed. Key Words: S-MIF-Archean atmosphere-Early Earth-Sulfur aerosols.

摘要

超过 2.45×10(9)年的沉积物中存在硫的质量独立分馏(S-MIF)被认为是早期缺氧大气存在的证据。紫外线(λ<220nm)对二氧化硫(SO(2))的光解已在模型和一些初步的实验室研究中显示可以产生 S-MIF;然而,硫必须以至少两种化学上不同的形式离开大气才能保留任何 S-MIF 特征。两种通常被引用的可以离开大气的化学上不同的硫物种的例子是元素硫(S(8))和硫酸(H(2)SO(4))气溶胶。在这里,我们使用实时气溶胶质谱法直接检测当 SO(2) 在波长为 115 到 400nm 之间光解时形成的含硫气溶胶,以模拟紫外线太阳光谱,或与高能电子相互作用,以模拟闪电。我们发现,在所有实验室条件下都形成了含硫气溶胶。此外,在我们的实验中添加了一种还原剂,氢气(H(2))或甲烷(CH(4)),增加了 S(8)的形成。在紫外线光解下,S(8)气溶胶的形成高度依赖于初始 SO(2)压力;并且在没有还原剂的情况下,仅在 2%的 SO(2)混合比和更高的情况下形成 S(8),在存在 1000ppm CH(4)的情况下,在 0.2%的 SO(2)混合比和更高的情况下形成 S(8)。我们还发现,有机硫化合物是由 CH(4)和适量 SO(2)的光解形成的。讨论了硫气溶胶对早期地球的影响。关键词:S-MIF-太古宙大气-早期地球-硫气溶胶。

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