Microfluidic study of evaporation-driven crystallization of saline and ammonia brines under hydrogen flow
Year: 2026
Type: article
Abstract: Underground hydrogen storage in geological formations is critical for renewable energy integration, but salt precipitation during gas injection can impair storage performance. While well studied for CO 2 systems, precipitation mechanisms in hydrogen–brine and ammonia–brine systems remain poorly understood. This study presents a systematic microfluidic investigation of salt crystallization during hydrogen injection into saline and ammonia-containing brine aquifers under high pressure with varying compositions (1–5 mol/kg NaCl), chemical additives (surfactants, alcohols, ammonia), and hydrogen flow rates (200–1300 mL/min). Quantitative imaging shows hydrogen induces physical precipitation through evaporation and capillary trapping, resulting in discrete deposits, whereas CO 2 -ammonia systems produce interconnected ammonium bicarbonate networks. Interfacial tension controls brine distribution and crystal coverage: high-IFT fluids form large pools promoting crystallization, low-IFT fluids form isolated pools reducing coverage by 50%. Alcohols and surfactants suppress precipitation, while ammonia increases crystal fraction. Higher flow rates accelerate crystallization, highlighting gas-specific mitigation strategies for underground hydrogen storage. • H 2 injection triggers salt precipitation via evaporation and capillary trapping. • Ammonia-rich brines accelerate precipitation on secondary substrates. • Post-breakthrough water saturation is spatially variable due to high H 2 mobility. • Crystal shape and distribution follow residual brine size and connectivity. • Additives change surface tension, shifting brine flow and growth sites.
Institutions: AGH University of Krakow, University of Oslo, SINTEF, SINTEF Industry
Language: English
Subfield: Environmental Engineering
Field: Environmental Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $3,730
Funder: EEA Grants
OpenAlex ID: W7130338097
