TY - JOUR
T1 - Evaporation and breakup behavior of high-pressure liquid ammonia sprays under various thermal conditions
AU - Yu, Zhiqing
AU - Shlenov, Matvel
AU - Markov, Vladimir
AU - Gao, Jianbing
AU - Zhao, Jianhui
N1 - Publisher Copyright:
© 2026 Elsevier Ltd.
PY - 2026/8
Y1 - 2026/8
N2 - As a zero‑carbon fuel, the atomization and evaporation characteristics of liquid ammonia are key to achieving efficient engine application. Diffuse back-illumination and Z-type schlieren imaging were used to investigate the effects of ambient conditions (300–500 K, 0.1–1.5 MPa) on liquid ammonia spray characteristics at 105 MPa injection pressure, revealing the dominant mechanisms governing spray development. The results show that ambient temperature and pressure play a significant regulatory role in spray morphology. Under low temperature and low pressure, flash boiling causes lateral expansion of the spray and a barb-like edge. When the ambient pressure increases to 1.0 MPa or above, flash boiling is suppressed and the spray transitions into a cold jet with greater penetration capability. Under high temperature, evaporation dominates, leading to rapid vaporization of the liquid phase and a narrowed spray contour. To characterize the spray regimes under different conditions, the characteristic parameter ratio ξ and the dimensionless temperature τ are introduced, dividing the development process of liquid ammonia sprays into three regimes: breakup-dominated, synergistic, and evaporation-dominated. The typical spray structure features of each regime are elucidated. Penetration models for liquid and gas phases incorporating the Weber and Ohnesorge numbers are established, achieving R 2 ranges of 0.935–0.994 (liquid) and 0.873–0.982 (gas), indicating good predictive accuracy across ambient conditions. Analysis based on the proposed models shows that inertial forces drive spray development, while viscous forces substantially inhibit it, and the synergistic effects of the two govern the development of liquid ammonia sprays.
AB - As a zero‑carbon fuel, the atomization and evaporation characteristics of liquid ammonia are key to achieving efficient engine application. Diffuse back-illumination and Z-type schlieren imaging were used to investigate the effects of ambient conditions (300–500 K, 0.1–1.5 MPa) on liquid ammonia spray characteristics at 105 MPa injection pressure, revealing the dominant mechanisms governing spray development. The results show that ambient temperature and pressure play a significant regulatory role in spray morphology. Under low temperature and low pressure, flash boiling causes lateral expansion of the spray and a barb-like edge. When the ambient pressure increases to 1.0 MPa or above, flash boiling is suppressed and the spray transitions into a cold jet with greater penetration capability. Under high temperature, evaporation dominates, leading to rapid vaporization of the liquid phase and a narrowed spray contour. To characterize the spray regimes under different conditions, the characteristic parameter ratio ξ and the dimensionless temperature τ are introduced, dividing the development process of liquid ammonia sprays into three regimes: breakup-dominated, synergistic, and evaporation-dominated. The typical spray structure features of each regime are elucidated. Penetration models for liquid and gas phases incorporating the Weber and Ohnesorge numbers are established, achieving R 2 ranges of 0.935–0.994 (liquid) and 0.873–0.982 (gas), indicating good predictive accuracy across ambient conditions. Analysis based on the proposed models shows that inertial forces drive spray development, while viscous forces substantially inhibit it, and the synergistic effects of the two govern the development of liquid ammonia sprays.
KW - Flash boiling
KW - Liquid ammonia
KW - Spray penetration model
KW - Spray regime
KW - Visualization experiment
UR - https://www.scopus.com/pages/publications/105044212213
U2 - 10.1016/j.applthermaleng.2026.132257
DO - 10.1016/j.applthermaleng.2026.132257
M3 - Article
AN - SCOPUS:105044212213
SN - 1359-4311
VL - 303
JO - Applied Thermal Engineering
JF - Applied Thermal Engineering
M1 - 132257
ER -