Perturbed and Unperturbed: Analyzing the Conservatively Perturbed Equilibrium (Linear Case)

The “conservatively perturbed equilibrium” (CPE) technique for a complex chemical system is computationally analyzed in a batch reactor considering different linear mechanisms with three and four species. Contrary to traditional chemical relaxation procedures, in CPE experiments only some initial concentrations are modified; other conditions, including the total amount of chemical elements and temperature are kept unchanged. Generally, for “unperturbed” species with initial concentrations equal to their corresponding equilibrium concentrations, unavoidable extreme values are observed during relaxation to the equilibrium. If the unperturbed species is involved in one step only, this extremum is a momentary equilibrium of the step; if the unperturbed species is involved in more reactions, the extremum is not a momentary equilibrium. The acyclic mechanism with four species may exhibit two extrema and an inflection point, which corresponds to an extremum of the rate of the species change. These facts provide essential information about the detailed mechanism of the complex reaction.

Erroneous or Arrhenius: A Degradation Rate-Based Model for EPDM during Homogeneous Ageing

To improve the predictive capability of long-term stress relaxation of elastomers during thermo-oxidative ageing, a method to separate reversible and irreversible processes was adopted. The separation is performed through the analysis of compression set after tempering. On the basis of this separation, a numerical model for long-term stress relaxation during homogeneous ageing is proposed. The model consists of an additive contribution of physical and chemical relaxation. Computer simulations of compression stress relaxation were performed for long ageing times and the results were validated with the Arrhenius treatment, the kinetic study and the time-temperature superposition technique based on experimental data. For chemical relaxation, two decay functions are introduced each with an activation energy and a degradative process. The first process with the lower activation energy dominates at lower ageing times, while the second one with the higher activation energy at longer ageing times. A degradation-rate based model for the evolution of each process and its contribution to the total system during homogeneous ageing is proposed. The main advantage of the model is the possibility to quickly validate the interpolation at lower temperatures within the range of slower chemical processes without forcing a straight-line extrapolation.

Chemical relaxation in porous ionic–electronic conducting materials represented by the distribution of characteristic times

Distribution of characteristic times (DCT) is proposed to resolve chemical relaxation in porous MIECs and to estimate kinetic parameters.

Measuring oxygen surface exchange kinetics on mixed-conducting composites by electrical conductivity relaxation

Chemical relaxation experiments in reducing atmospheres show little to no contribution of heterogeneous phase-boundaries to oxygen surface exchange kinetics on Sr2Fe1.5Mo0.5O6−δ–Sm0.2Ce0.8O2−δ dual-phase composites.