热力学的加性单原子值II:离子固体形成的焓、熵和吉布斯能

Leslie Glasser
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摘要

在本系列的第一部分中,我们为每种化学元素建立了公式体积、绝对熵、恒压热容及其温度系数的优化总和。这些原子值,当求和成化学式时,提供了该化学物质相应性质的零水平估计。由于化学元素的数量有限,原子和具有本质上完整的特殊优点,可用于预测和检验化学材料的值。然而,这样做的代价是不能区分具有相同化学式的异构体和相,也不能考虑原子相互作用的影响。在本出版物中,我们提出了生成熵、生成焓及其与生成吉布斯能的关系的优化原子和。为了检验结果的可靠性,对使用DFT计算的每种预测方法、专有的基团贡献方法和提出的单原子和方法进行了比较。发现单原子和法最适合作为大生成熵和大生成焓值的初始估计,其中包括离子水合物。元素对元素周期表中基团的能量贡献,使得严格的原子独立性和加性不占主导地位,而熵项相对恒定(对于非气态元素),这意味着原子的行为是独立的,因此在贡献由它们在离子固体中的振动产生的熵项时是加性的。这可能是由这个单原子和集合产生的独特演示。这现在包括一套完整的简单的零级热力学预测和检查,这应该是补充任何其他资源可供研究人员使用。
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Additive single atom values for thermodynamics II: Enthalpies, entropies and Gibbs energies for formation of ionic solids

In part I of this series we established optimised sum values, for each of the chemical elements, of formula volumes, of absolute entropies, and of constant pressure heat capacities, together with their temperature coefficients. These atom values, when summed for a chemical formula, provided zero-level estimates of the corresponding property of that chemical material. Atom sums have the particular advantage of being essentially complete because of the finite number of chemical elements and are of use in prediction and checking of values for chemical materials. However, this is at the expense of an inability to distinguish among isomers and phases with the same chemical formula nor do they allow for effects of atom interactions.

In the present publication, we present optimised atom sums for formation entropies, formation enthalpies and their relation to formation Gibbs energies.

In order to check the reliability of the results, comparison is made among methods of prediction using each of DFT calculations, a proprietary group contribution method, and the proposed single atom sum method. The single atom sum method is found to be most suitable as an initial estimate for large formation entropies and also for large values of formation enthalpies, which includes ionic hydrates.

The energy contributions of the elements group into the Groups of the Periodic Table so that strict atom independence and thus additivity is not predominant while entropy terms are relatively constant (for the non-gaseous elements) implying that the atoms behave independently and thus additively in contributing to the entropy terms resulting from their vibrations within the ionic solids. This is possibly a unique demonstration resulting from this single atom sum collection.

This now comprises a complete set for simple zero-order thermodynamic prediction and for checking, which should be complemented by whatever other resources are available to the researcher.

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