Transitory Sensitivity in Automatic Chemical Kinetic Mechanism Analysis

30 January 2024, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Detailed chemical kinetic mechanisms are necessary for resolving many important chemical processes. As the field has advanced, kineticists have become interested in constructing progressively larger kinetic mechanisms to model increasingly complex chemical processes. These large kinetic mechanisms prove incredibly difficult to refine and time-consuming to interpret. Traditional sensitivity analysis on a large mechanism can range from inconvenient to practically impossible without special techniques to reduce the computational cost. We first present a new time-local sensitivity analysis we term transitory sensitivity analysis. Transitory sensitivity analysis is demonstrated in an example to accurately identify traditionally sensitive reactions at an 18,000x speed up over traditional sensitivities. By fusing transitory sensitivity analysis with more traditional time-local branching, pathway and cluster analyses, we develop an algorithm for efficient automatic mechanism analysis. This automatic mechanism analysis at a time point is able to identify the reactions a target is most sensitive to using transitory sensitivity analysis and then propose hypotheses why the reaction might be sensitive using branching, pathway, and cluster analyses. We implement these algorithms within the Reaction Mechanism Simulator (RMS) package, which enables us to report the the automatic mechanism analysis results in highly readable text format and in molecular flux diagrams.

Keywords

chemical kinetics
sensitivity analysis
kinetic mechanism analysis

Supplementary materials

Title
Description
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Title
Description of the Timescale Identification Algorithm
Description
Describes the timescale identification algorithm used in the main text.
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