Difference between revisions of "orch:Solvers"
From orch
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− | \mathcal{Q} = \mathcal{Q} | + | \mathcal{Q}_j = \mathcal{Q}_{f,j} - \mathcal{Q}_{r,j} |
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Revision as of 13:51, 7 March 2016
Contents
Solver to build reference trajectories
DRGEP solver for species reduction
- Compute species direct inter-relations
- Compute species relations through indirect paths
- Compute relations between targets and
DRGEP solver for reactions reduction
QSS solver
- Solve for thermodynamic
Get Gibbs Free Energy
Get Equilibrium constants
Chemical kinetics
- Arrhenius law
The global rate of a reaction (evolution in concentration per unit of time) varies depending on the proportion of the rates associated to the forward and backward directions.
- Three-body reactions
In the forward direction, three-body reactions involve two species A and B as reactants and yield a single product AB. In that case, the third body M is used to stabilize the excited product AB*. On the contrary, in the reverse direction, heat provides the energy necessary to break the link between A and B.
The third body M can be any inert molecule.