Pyrolysis
bio-oil (PBO), a renewable and sustainable alternative
energy source, is gaining significant importance. PBOs are polar,
viscous, and acidic in nature, which restrict their direct utilization.
The blending of PBOs with fossil-based fuels in combustion processes
can potentially reduce net carbon emissions. The utilization of PBOs
in combustion systems warrants an understanding of their combustion
chemistry, which serves as the motivation for this study. In this
study, pyrolysis of a saltwater halophyte, Salicornia
bigelovii, was performed to obtain PBO. Based on the
PBO composition, a blend of pyrrole, furfural, and toluene was prepared
as a surrogate. The combustion chemistry of a three-component surrogate
comprising oxygen- and nitrogen-containing compounds is studied for
the first time. To understand the gas-phase combustion chemistry of
the PBO surrogate, experiments were performed in a jet-stirred reactor
(JSR) at atmospheric pressure and a residence time of 2 s in the temperature
range of 780–960 K (ϕ = 0.25). Also, the PBO surrogate
was blended in the ratios of 10 and 20% (by wt) with a toluene/iso-octane
(80/20 mol/mol) mixture and investigated to mimic the combustion of
PBO with hydrocarbons. A detailed chemical kinetic mechanism was compiled
using different sub-mechanisms for surrogate components. NUIGMech1.2
was used as the base mechanism. Fuel-reactant species and 17 product
species were identified to understand the combustion chemistry of
PBO surrogate and its blends. Furthermore, rate of production analysis
was performed to understand the pathways vital for forming intermediates.
In addition, the thermal stability of PBO was studied in a thermogravimetric
analyzer in the temperature range of 105–750 °C in oxygen
and nitrogen atmospheres. The mass loss and derivative mass loss profiles
were acquired, different stages of the reactions were identified under
the oxygen atmosphere, and the apparent kinetic parameters were determined
via the Friedman method.