Steepest-Entropy-Ascent Framework for Predicting Arsenic Adsorption on Graphene Oxide Surfaces: A Case Study
Water contamination by arsenic(V) constitutes a major public-health concern, underscoring the need for models that capture both equilibrium and transient adsorption behavior. A framework that can do so is the steepest-entropy-ascent quantum thermodynamic (SEAQT) framework, which is used here to describe the uptake of As(V) on graphene oxide (GO) across pollutant concentrations of 25-350 mg L<sup>-1</sup>. A nonequilibrium equation of motion derived from the steepest-entropy-ascent principle for a five-component system (water, arsenic, two GO functional groups, and H<sup>+</sup>) is solved with an energy eigenstructure generated by a Replica-Exchange Wang-Landau algorithm and then extrapolated to relevant contaminant concentrations via an artificial neural network. Without recourse to empirical rate laws, the model predicts the time-dependent adsorption capacity, the stable-equilibrium arsenic concentration, and the pH dependence of removal efficiency. Equilibrium capacities are reproduced within 5% of experimental isotherms, and the characteristic adsorption time aligns with the reported kinetics. These results indicate that SEAQT framework provides a thermodynamically consistent, fully predictive tool for designing and optimizing adsorbent-based water-treatment technologies.
Authors
- César Damián (ORCID: https://orcid.org/0000-0003-4515-6570)
- Michael R. von Spakovsky (ORCID: https://orcid.org/0000-0002-3884-6904)
- W. T. Reynolds (ORCID: https://orcid.org/0000-0002-7568-3104)
- Adriana Saldaña‐Robles (ORCID: https://orcid.org/0000-0001-8871-1621)
Institutions
- Universidad de Guanajuato (MX)
- Division of Materials Science and Engineering (AU)
- Virginia Tech (US)
Publication Details
- Journal
- Journal of Chemical Information and Modeling
- Published
- 2025-06-16
- DOI
- https://doi.org/10.1021/acs.jcim.5c00672
- Citations
- 1
- Primary Topic
- Electrochemical Analysis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.52