However, it is challenging to directly model this system due to the vast differences in length scale between supramolecular nanofibers and the macroscopic tube.
Thus, a bi-dimensional birth and death process is required for modeling this system.
We have used time automata framework to model this system by extracting real time constraints from this safety critical system.
We modeled this system as four tubular reactors in series allowing the enzyme concentration to vary in each compartment.
Anyone who intends to model this system will look at existing models to adapt, refine and improve them.
These numbers indeed explain why the Debye- Huckel treatment is a reasonable starting point for modeling this system.
We have modelled this system by cellular automata on a regular grid, as we believe this is the most suitable description.
Grinberg and Rappe and their colleagues modeled this system using density functional theory with clusters of 6 to 8 cells having various distributions of Zr4+ and Ti4+ cations.
These results highlight the need for additional experiments and further theoretical calculations to accurately model this unique system.
