Tosti Silvano
Nuclear Department, ENEA, Via E. Fermi 45, 00044 Frascati, Italy.
Entropy (Basel). 2024 Oct 21;26(10):884. doi: 10.3390/e26100884.
This work recalls the basic thermodynamics of chemical processes for introducing the evaluation of the nuclear reactions' spontaneity. The application and definition of the thermodynamic state functions of the nuclear processes have been described by focusing on their contribution to the chemical potential. The variation of the nuclear binding potentials involved in a nuclear reaction affects the chemical potential through a modification of the internal energy and of the other state functions. These energy changes are related to the mass defect between reactants and products of the nuclear reaction and are of the order of magnitude of 1 MeV per particle, about six orders of magnitude larger than those of the chemical reactions. In particular, this work assesses the Gibbs free energy change of the fusion reactions by assuming the as the nuclear contribution to the chemical potential and by calculating the entropy through the Sackur-Tetrode expression. Then, the role of the entropy in fusion processes was re-examined by demonstrating the previous spontaneity analyses, which assume a perfect gas of DT atoms in the initial state of the fusion reactions, are conservative and lead to assessing more negative ΔG than in the real case (ionized gas). As a final point, this paper examines the thermodynamic spontaneity of exothermic processes with a negative change of entropy and discusses the different thermodynamic spontaneity exhibited by the DT fusion processes when conducted in a controlled or uncontrolled way.
这项工作回顾了化学过程的基本热力学,以引入对核反应自发性的评估。通过关注核过程的热力学状态函数对化学势的贡献,描述了它们的应用和定义。核反应中涉及的核结合能的变化通过内能和其他状态函数的改变来影响化学势。这些能量变化与核反应反应物和产物之间的质量亏损有关,每个粒子的量级约为1兆电子伏特,比化学反应的能量变化大六个数量级左右。特别是,这项工作通过假设 作为对化学势的核贡献,并通过Sackur-Tetrode表达式计算熵,来评估聚变反应的吉布斯自由能变化。然后,通过证明先前的自发性分析(假设聚变反应初始状态为DT原子的理想气体)是保守的,并且导致评估出比实际情况(电离气体)更负的ΔG,重新审视了熵在聚变过程中的作用。最后,本文研究了熵变负的放热过程的热力学自发性,并讨论了DT聚变过程在受控或不受控方式下表现出的不同热力学自发性。