从原子结构角度审视电子相变理论

József Garai
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引用次数: 0

摘要

卢瑟福原子模型的缺点可以通过建议的电子在原子核附近从点电荷到非旋转表面电荷的相变来消除。对该原子模型的能量平衡研究表明,表面电荷价电子壳的稳定性是由一维卡西米尔效应保证的。如果这一理论预测是正确的,那么元素的首次电离能应与原子直径的倒数成线性关系。从经典物理学的角度来看,原子核的静电吸引力和表面电荷电子外壳的排斥力会产生相同的关系。经典物理学方法的问题在于它无法充分解释光电效应和金属内部的自由电子。因此,经典静电学不能被视为中性原子中价电子稳定的正确物理过程。推导出的原子直径与电离能之间的理论关系已在元素周期表的 86 个元素中进行了测试。相关系数为 0.9187。个别周期的相关性更强。电离能和原子半径之间的经验关系是众所周知的,因此得出了相同的相关系数。然而,与原子半径的相关性并没有再现理论上得出的常数乘数,这与原子直径的关系相反。因此,第一电离能是原子直径的函数。报告的原子尺寸的不确定性相对较高。因此,理论与实验之间的相关性应该被认为是非常好的。理论上得出的第一电离能与原子直径之间的关系是所提出的电子相变的结果。因此,检测到的理论与实验之间的强相关性进一步支持了所提出的原子结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Examining the Electron Phase Transformation Theory in the Context of Atomic Structure
The shortcomings of the Rutherford atomic model can be eliminated by the suggested phase transformation of the electrons from point to non-revolving surface charge in the vicinity of the nucleus. The energy balance investigations of this atom model indicated that the stability of the surface charge valence electron shell is ensured by the one-dimensional Casimir effect. If this theoretical prediction is correct then the first ionization energies of the elements should correlate linearly to the inverse of atomic diameter. Classical physics approach, the electrostatic attraction of the nucleus and the repulsion of the surface charge electron shell result in an identical relationship. The problem with the classical physics approach is that it does not offer an adequate explanation for the photoelectric effect and the free electrons inside the metal. Therefore, classical electrostatics cannot be considered the right physical process responsible for the stability of the valence electron/s in neutral atoms. The derived theoretical relationship, between atomic diameter and ionization energy, was tested up to 86 elements of the periodic table. The correlation coefficient is 0.9187. The correlation is stronger for individual periods. The empirical relationship between the ionization energy and atomic radii is well known, resulting in the same correlation coefficients. However, the correlation to the atomic radii does not reproduce the theoretically derived constant multiplier, contrarily to the atomic diameter relationship. Thus, the first ionization energy is the function of the atomic diameter. The uncertainties in the reported atomic sizes are relatively high. Therefore, the correlation between theory and experiments should be considered as excellent. The theoretically derived relationship between the first ionization energy and atomic diameter is the consequence of the proposed phase transformation of the electron. Thus the detected strong correlation between theory and experiments adds further support to the proposed atomic structure.
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