In this study, we present a theoretical method for evaluating ion and water coupling on a discrete-state diagram using a thermodynamic concept of cycle flux.
Furthermore, using a thermodynamic metabolic network analysis the metabolite measurements and metabolic flux directions were validated.
Using a solid-state electrochemical technique, thermodynamic properties of three sulfide phases (RhS0.882, Rh3S4, Rh2S3) in the binary system (Rh + S) are measured as a function of temperature over the range from (925 to 1275) K.
Using a simple corresponding states thermodynamic model, we relate the pressure effects to a decrease in the PS/heptane interaction parameter, i.e. an increase in the solvent quality with increasing pressure.
Nevertheless, because we were not able to find experimental conditions of reversibility for myoc-OLF, the extent of the validity of thermodynamic parameters obtained using a two-state model cannot be assessed.
Moreover, the optimization of redox state was successfully accomplished through fine-tuning of FDH1 based on a predictive method of controlling translation using a biophysical thermodynamic model of the translation initiation process (UTR Designer) [ 22].
By using a three-state model (FIU) [see the Supporting Information, Eq. (5 16)] with an intermediate I state, we double the number of thermodynamic parameters that could be interpreted and compared to the simple two-state analysis.
Binding free energy differences were calculated using a non-equilibrium thermodynamic integration scheme.
This dependency can be used to tailor the thermodynamic state of the coating prior to can production.
Free energy is an extensive property, meaning that its magnitude depends on the amount of a substance in a given thermodynamic state.
