Kinetics of Formic Acid Decomposition in Subcritical and Supercritical Water - A Raman Spectroscopic Study

06 February 2019, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The decomposition of formic acid is studied in a continuous sub- or supercritical water reactor at temperatures between 300 and 430°C, a pressure of 25 MPa, residence times between 4 and 65 s, and a feedstock concentration of 3.6 wt%. In-situ Raman spectroscopy is used to produce real-time data and accurately quantify decomposition product yields of H2, CO2, and CO. Collected spectra are used to determine global decomposition rates and kinetic rates for individual reaction pathways. First-order global Arrhenius parameters are determined as log A (s-1) = 1.6 ± 0.20 and EA = 9.5 ± 0.55 kcal/mol for subcritical decomposition, and log A (s-1) = 12.56 ± 1.96 and EA = 41.90 ± 6.08 kcal/mol for supercritical decomposition. Subcritical and supercritical Arrhenius parameters for individual pathways are proposed. The variance in rate parameters is likely due to changing thermophysical properties of water across the critical point. There is strong evidence for a surface catalyzed free-radical mechanism responsible for rapid decomposition above the critical point, facilitated by low density at supercritical conditions.

Keywords

Chemical Kinetics
Supercritical Water
Formic Acid
Raman
Gasification
Reaction Mechanisms

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