Difference between revisions of "orch:Solvers"

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(Chemical kinetics)
(Chemical kinetics)
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k_j = \mathcal{A}_j T^{\mathcal{\beta}_j} \exp \left(-\frac{E_{a_j}}{R T}\right)
 
k_j = \mathcal{A}_j T^{\mathcal{\beta}_j} \exp \left(-\frac{E_{a_j}}{R T}\right)
 
</math>
 
</math>
 +
  
 
* Reaction rates
 
* Reaction rates
Line 47: Line 48:
 
\mathcal{Q}_j = \mathcal{Q}_{f,j} - \mathcal{Q}_{r,j}  
 
\mathcal{Q}_j = \mathcal{Q}_{f,j} - \mathcal{Q}_{r,j}  
 
</math>
 
</math>
 +
  
 
* Production/Consumption source terms
 
* Production/Consumption source terms

Revision as of 14:04, 7 March 2016

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

is the pre-exponential factor, is the temperature exponent and the activation energy


  • Reaction rates

The global rate of a reaction j (evolution in concentration per unit of time) varies depending on the proportion of the rates associated to the forward and backward directions.


  • Production/Consumption source terms

species source terms are deduced from

  • 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.