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The observed inconsistency is largely due to differences in the calculation of equilibrium codon frequencies, which one has to estimate to calculate Ks (see supplementary figs. S3 S6, Supplementary Material online, for a comparison of Ks distributions of P. infestans, P. ramorum, and P. sojae under different models of codon frequencies).
The other aim of this paper was to characterize various engineering methods used in the calculation of equilibrium gasification processes.
Accurate calculation of equilibrium formation conditions of hydrates is important for gas storage and separation based on hydrate technology.
Critically selected thermodynamic data have been used for the calculation of equilibrium conditions in the vanadium-water system at 298·15K.
This paper reports a comparative study on the calculation of equilibrium potential (also known as Open Circuit Voltage) of co-electrolysis of H2O and CO2 in a Solid Oxide Electrolyzer Cell.
The application of statistical methods of continuous thermodynamics enables not only the calculation of equilibrium composition but also provides facilities for the demonstration of very interesting and striking regularities in behavior.
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This work presents how to deal with calculations of equilibrium shift in a membrane reactor using Gibbs free energy minimization method.
Theoretical calculations of equilibrium Si contents required to prevent the formation of Al4C3 in the SiC/Al composite were performed by taking the variations in Al and Si activities as well as those of other compounds into account for the calculations.
Calculations of equilibrium characteristics were based on minimizing the thermodynamic potential of the system.
In calculations of equilibrium quotients, activity of water in Eq. (25) below 75°C is taken from Gibbard et al. [25], and at T ≥ 75°C is taken from Liu and Lindsay [42], and the logK° at the above temperatures are taken from Brown et al. [80].
The equation allows the calculation of the equilibrium constant, or the relative amounts of products and reactants present at equilibrium, from measured or derived values of standard free energies of substances.
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