Premium
Nitrogen‐Driven Chromatographic Separation During Gas Injection Into Hydrate‐Bearing Sediments
Author(s) -
Darnell K. N.,
Flemings P. B.,
DiCarlo D.
Publication year - 2019
Publication title -
water resources research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.863
H-Index - 217
eISSN - 1944-7973
pISSN - 0043-1397
DOI - 10.1029/2018wr023414
Subject(s) - hydrate , clathrate hydrate , phase (matter) , molecule , natural gas , component (thermodynamics) , nitrogen , chemistry , multiphase flow , chemical engineering , petroleum engineering , chromatography , chemical physics , materials science , geology , thermodynamics , organic chemistry , physics , engineering
Hydrates are solid phases composed of water cages enclosing gas molecules that may host large quantities of recoverable natural gas and may serve to sequester CO 2 on geological time scales. Most hydrate studies focus on hydrates containing a single gas component, such as CH 4 or CO 2 . Yet, there are several settings in which multiple components form hydrate mixtures, or mixed hydrates, including a subsurface injection technique that claims to simultaneously recover CH 4 and sequester CO 2 called “guest molecule exchange.” Here, we combine multicomponent phase behavior for hydrate‐forming systems with a multiphase fluid flow simulator to understand the evolution of hydrate and nonhydrate phases during subsurface injection. We simulate various scenarios for systems composed of H 2 O, CH 4 , CO 2 , and N 2 . Our study probes the impact of injection composition, initial reservoir composition, and transport of each component through the model domain. We observe chromatographic separation from the combined effect of compositional partitioning in each phase, variable flow speed of each phase, and compositional dependence of phase stabilities. We show that N 2 drives chromatographic separation to create a CH 4 ‐free zone and a CO 2 ‐free zone that are connected by a continuous N 2 ‐dominated vapor phase. While our results are theoretical and should be validated experimentally, they imply that guest molecule exchange acts as two sequential processes rather than as a simultaneous process. Furthermore, they show that injections into reservoirs with and without free water have vastly different behaviors, which has implications for the interpretation of the guest molecule exchange field test and various laboratory studies.