Rush-to-equilibrium concept for minimizing reactive nitrogen emissions in ammonia combustion

Abstract

Ammonia (NH3) is a zero-carbon fuel that has been receiving increasing attention for power generation and even transportation. Compared to H2, NH3's volumetric energy density is higher, is not as explosive, and has well established transport and storage technologies. Yet, NH3 has poor flammability and flame stability characteristics and more reactive nitrogen (RN: NOx, N2O) emissions than hydrocarbon fuels, at least with traditional combustion processes. Partially cracking NH3 (into a NH3-H2-N2 mixture, AHN) addresses its flammability and stability issues. RN emissions remain a challenge, and mechanisms of their emissions are fundamentally different in NH3 and hydrocarbon combustion. While rich-quench-lean NH3 combustion strategies have shown promise, the largest contributions to RN emissions are the unrelaxed emissions in the fuel-rich stage due to overshoot of thermodynamic equilibrium within the reaction zone of premixed flames coupled with finite residence times available for relaxation to equilibrium. This work introduces a rush-to-equilibrium concept for AHN combustion, which aims to reduce the unrelaxed RN emissions in finite residence times by accelerating the approach to equilibrium. In the concept, a flow particle is subjected to a decaying mixing rate as it transits the premixed flame. This mitigates the mixing effects that prevents the particle approach to equilibrium, and promotes the chemistry effects to push the particle toward equilibrium, all while considering finite residence times. Evaluated with a state-of-the-art combustion model at gas turbine conditions, the concept shows the potential to reduce RN emissions by an order of magnitude, and that works irrespective of cracking extent, pressure, temperature, etc. A brief discussion of possible practical implementation reveals reasonable geometric and flow parameters characteristic of modern gas turbine combustors.