Difference between revisions of "orch:Solvers"

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(DRGEP solver for species reduction)
(Chemical kinetics)
Line 39: Line 39:
 
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.  
 
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.  
  
<math>\mathcal{Q} = \mathcal{Q}_f - \mathcal{Q}_r </math>
+
<math>
 +
\mathcal{Q} = \mathcal{Q}_f - \mathcal{Q}_r  
 +
</math>
  
 +
 +
<math>
 +
\dot{\omega}_k = c_k - d_k
 +
</math>
  
 
* Three-body reactions
 
* Three-body reactions

Revision as of 14:50, 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


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.