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Temporal reversibility of reactive systems out of equilibrium: Molecular dynamics simulation

2024/10/25 by O. Politano, Politano, O., Alejandro L. Garcia +5
Chemistry · Engineering · Physics and Astronomy · #Advanced Thermodynamics and Statistical Mechanics #Chemical Physics (physics.chem-ph) #FOS: Physical sciences #Phase Equilibria and Thermodynamics #Statistical Mechanics (cond-mat.stat-mech) #thermodynamics and calorimetric analyses

paper · pdf · doi:10.48550/arxiv.2410.19578

openalex publication_date 2024/10/25 · openalex created_date 2024/11/14 · openalex updated_date 2026/07/31

Abstract

The second law of thermodynamics states that entropy production in macroscopic systems is non-negative, reaching zero only at thermodynamic equilibrium. As a corollary, this implies that the state trajectory of macroscopic systems is inherently time-irreversible under out-of-equilibrium conditions. However, over the past half-century, various studies have shown that this principle does not universally apply to the composition sample paths of certain isothermal reactive systems. Theoretical frameworks leading to this surprising observation primarily focus on perfectly homogeneous systems (often referred to as zero-dimensional systems), which inherently exclude the effects of local fluctuations. This oversimplification may account for the paradoxical theoretical predictions. In the absence of relevant experimental data, this paper seeks to explore this phenomenon through microscopic simulations.

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