EN General thermodynamic relations for thermal variables formed by first-order partial derivatives and not mixed second-order derivatives

О.В. Троценко
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Abstract

The theory of differential equations is a powerful tool necessary for constructing mathematical models of various applied problems and their solution. The study and analysis of the general differential relations between the derivatives of the thermodynamic functions of substances is a new direction in the theory of their thermodynamic properties. This research is the development of thermodynamics associated with the establishment and use of differential equations. This paper presents two new thermodynamic relationships between thermal variables pressure, absolute temperature, and specific volume. They relate first-order partial derivatives with unmixed second-order derivatives for these variables. Revealing new general relations of thermodynamics made it possible to formulate and solve a number of problems, among which we can note: creation of algorithms for calculating second-order mixed derivatives for a given thermal equation of state; analysis of the features of the second mixed derivatives at the critical point of pure substance; investigations of the general thermodynamic equations with entropy. The procedure for establishing new equations is based on the use of a rigorous mathematical apparatus and Maxwell's differential equations. Therefore, they are of a general nature, that is, they are valid for any pure substance or any mixture of fixed composition. They are also applicable to any model of the equation of state of these substances. With a formal approach to the concept of the term "equation of state", the new relations themselves can be considered as the equation of state of substance. The obtained new relations can be used to develop the theory of the thermodynamic properties of substances. In particular, in this work it is shown that the ratios of two partial derivatives of pressure over the volume, which are zero critical conditions, have no singularities at the critical point itself
由一阶偏导数和非混合二阶导数形成的热变量的一般热力学关系
微分方程理论是构建各种应用问题的数学模型及其求解所必需的有力工具。研究和分析物质热力学函数导数之间的一般微分关系,是研究物质热力学性质理论的一个新方向。这项研究是热力学的发展与微分方程的建立和使用有关。本文提出了压强、绝对温度和比容之间的两种新的热力学关系。他们把这些变量的一阶偏导数和未混合二阶导数联系起来。揭示新的热力学一般关系使我们有可能表述和解决许多问题,其中我们可以注意到:对于给定的热状态方程,创建了计算二阶混合导数的算法;纯物质临界点下二阶混合导数的特征分析带熵的一般热力学方程的研究。建立新方程的程序是基于使用严格的数学设备和麦克斯韦微分方程。因此,它们具有普遍性,也就是说,它们对任何纯物质或任何固定成分的混合物都有效。它们也适用于这些物质的状态方程的任何模型。通过对“状态方程”概念的形式化处理,新的关系本身可以被认为是物质状态方程。所得的新关系可用于发展物质的热力学性质理论。特别地,在这项工作中,证明了压力对体积的两个偏导数之比,在零临界条件下,在临界点本身没有奇点
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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