Amino acid-assisted effect on hydrate-based CO2 storage in porous media with brine

CO2 storage as hydrates in porous media is a promising method for storing carbon dioxide (CO2). However, the sluggish formation kinetics of hydrates urge the need to focus on the use of additives (promoters) to accelerate hydrate kinetics. This study investigates the effect of amino acid solutions in brine on CO2 hydrate formation and dissociation kinetics in quartz sand particles QS-2 (0.6-0.8 mm) with 38% porosity. The amino acids L-methionine (L-meth), L-isoleucine (L-iso), and L-threonine (L-threo) were studied at 0.2 wt% using an autoclave hydrate reactor at 4 MPa and 274.15 K in the presence and absence of salt (3.3 wt% NaCl) in 100% water saturation. The hydrate dissociation kinetics was studied at a temperature of 277.15 K. These conditions represent the normal seabed temperature range in Malaysia and hence were used for testing CO2 hydrate formation and dissociation kinetics in quartz sand in this study. Further, CO2 hydrate formation and dissociation experiments were conducted with sodium dodecyl sulphate (SDS) and brine systems as standards for comparison. The findings reveal the best kinetics for L-meth exhibiting the highest CO2 hydrate storage capacity. L-meth recorded a gas-to-hydrate conversion ratio of about 93% at 0.2 wt% in quartz sand with brine. Moreover, L-meth exhibited the lowest hydrate dissociation rate compared to L-iso and L-threo systems, thereby enhancing CO2 hydrate stability in quartz sand. Comparatively, L-meth enhanced the storage capacity by 36% and reduced the induction time by more than 50% compared to conventional promoter SDS in quartz sand with brine, suggesting it to be favorable for CO2 storage applications. CO2 hydrate nucleation time was predicted in quartz sand with and without the best-studied amino acid L-meth system with high prediction accuracy and an absolute average deviation of 2.4 hours. The findings of this study substantiate the influence of amino acids in promoting the storage capacity of CO2 in sediments as hydrates.