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DYNAMIC HYDROGEN IONIZATION

机译:动态氢电离

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摘要

We investigate the ionization of hydrogen in a dynamic solar atmosphere. The simulations include a detailed non-LTE treatment of hydrogen, calcium, and helium but lack other important elements. Furthermore, the omission of magnetic fields and the one-dimensional approach make the modeling unrealistic in the upper chromosphere and higher. We discuss these limitations and show that the main results remain valid for any reasonable chromospheric conditions. As in the static case, we find that the ionization of hydrogen in the chromosphere is dominated by collisional excitation in the Lyα transition followed by phofoionization by Balmer continuum photons―the Lyman continuum does not play any significant role. In the transition region, collisional ionization from the ground state becomes the primary process. We show that the timescale for ionization/recombination can be estimated from the eigenvalues of a modified rate matrix where the optically thick Lyman transitions that are in detailed balance have been excluded. We find that the timescale for ionization/recombination is dominated by the slow collisional leakage from the ground state to the first excited state. Throughout the chromosphere the timescale is long (10~3-10~5 s), except in shocks where the increased temperature and density shorten the timescale for ionization/recombination, especially in the upper chromosphere. Because the relaxation timescale is much longer than dynamic timescales, hydrogen ionization does not have time to reach its equilibrium value and its fluctuations are much smaller than the variation of its statistical equilibrium value appropriate for the instantaneous conditions. Because the ionization and recombination rates increase with increasing temperature and density, ionization in shocks is more rapid than recombination behind them. Therefore, the ionization state tends to represent the higher temperature of the shocks, and the mean electron density is up to a factor of 6 higher than the electron density calculated in statistical equilibrium from the mean atmosphere. The simulations show that a static picture and a dynamic picture of the chromosphere are fundamentally different and that time variations are crucial for our understanding of the chromosphere itself and the spectral features formed there.
机译:我们研究动态太阳气氛中氢的电离。模拟包括氢,钙和氦的详细非LTE处理,但缺少其他重要元素。此外,磁场的遗漏和一维方法使得在上色球层及更高色球层中的建模不现实。我们讨论了这些局限性,并表明主要结果在任何合理的色球条件下仍然有效。与静态情况一样,我们发现色球中氢的电离作用主要由Lyα跃迁中的碰撞激发以及随后的Balmer连续光子进行光离化作用——Lyman连续体没有任何重要作用。在过渡区域中,从基态发生碰撞电离成为主要过程。我们表明,电离/重组的时间尺度可以从修改后的速率矩阵的特征值中估算出来,在该速率矩阵中,光学上较厚的莱曼跃迁在详细平衡中已被排除在外。我们发现电离/重组的时间尺度主要是从基态到第一激发态的缓慢碰撞泄漏。在整个色球层中,时间尺度很长(10〜3-10〜5 s),但在激增中,温度和密度升高会缩短电离/重组的时间尺度,特别是在上色球层中。因为弛豫时间尺度比动态时间尺度长得多,所以氢离子化没有时间达到其平衡值,并且其波动远小于适用于瞬时条件的统计平衡值的变化。由于电离和重组率随温度和密度的增加而增加,因此电击中的电离比电击和电离后的复合更快。因此,电离态倾向于代表较高的电击温度,平均电子密度比从平均大气统计平衡计算出的电子密度高6倍。仿真表明,色球的静态图片和动态图片根本不同,并且时间变化对于我们了解色球本身及其形成的光谱特征至关重要。

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