High-Pressure Oxidation of Ammonia Mixed with Dimethoxymethane

The oxidation of ammonia-dimethoxymethane (NH3-DMM)
mixtures at high pressure was analyzed from both experimental and
kinetic modeling points of view. Experiments were performed using
a laboratory tubular flow reactor installation and were conducted
at 10, 20, and 40 bar under fuel-rich (λ = 0.7), stoichiometric
(λ = 1), and fuel-lean (λ = 3) conditions and temperatures
ranging from 650 to 1250 K. The inlet DMM concentration was varied
(100 and 200 ppm), keeping the concentration of ammonia constant at
1000 ppm. The data were interpreted in terms of a detailed chemical
kinetic model. Despite some discrepancy between the model predictions
and measurements, the model accurately followed the experimental trends,
highlighting its ability to describe the oxidation of the NH3-DMM mixture. The experimental and predicted results suggested that
the conversion of both ammonia and DMM was favored by increased pressure
and higher inlet concentrations of O2 and DMM. Under the
conditions of the present work, the dominant path for ammonia and
DMM conversion leads to N2/N2O and CO/CO2 in any case. Concentrations of NO and NO2 were
below the detection limit in all the experimental conditions studied,
which imply a benefit in the reduction of NOx emissions during the combustion of pure ammonia. DMM enhanced
the ammonia reactivity, although its presence leads to the formation
of CO2 not only by the common CO + OH reaction but also
through the interaction of N2O with CO.