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High-pressure Sapphire Cell for Phase Equilibria Measurements of CO2/Organic/Water Systems
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Structure-Preserving Excess Gibbs Learning for Multicomponent Phase Equilibria: A Falsifiable and Uncertainty-Aware
Pedro Robles1, Luis Rios-Colque2, Vanesa Bazan3,4
1Escuela de Ingeniería Química, Pontificia Universidad Católica de Valparaíso, Valparaíso 2340000, Chile.
Abstract:
This fully synthetic study tests a structure-preserving surrogate on NRTL-generated phase equilibrium systems; it contains no experimental molecular validation. A symmetric neural potential represents GE/(nRT), from which activity coefficients, thermal derivatives, binodals, flashes, and tangent-plane-distance diagnostics are derived. Across ten binary training seeds, its median lnγ MAE was 1.16×10-3, better than matched direct regression (2.40×10-3) but not Redlich-Kister (9.65×10-4) or correctly specified refitted NRTL (2.36×10-4). Gibbs-Duhem residuals decayed as O(h2) under grid refinement, confirming diagnostic truncation around an analytic identity. A 41,600-point binary hull gave endpoint MAE 2.31×10-4. On 100 ternary type-I feeds, phase-count agreement with numerical reference labels was 98.0% (exact 95% interval, 93.0-99.8%), with two false negatives after recovery of one infeasible-floor solver failure. A 20-member ensemble showed pooled error ranking (ρ=0.894) but weak in-domain ranking (ρ=0.164); a temperature-distance heuristic was stronger (ρ=0.914), and nominal 90% conformal coverage fell from 88.0% in-domain to 0.0% under shift. Controlled flashes were 2.77× slower than NRTL. A hard thermodynamic structure is therefore valuable within neural modeling, but classical dominance, shift sensitivity, and absent molecular data bound the claim.
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