TY - JOUR
T1 - Zwitterionic polymeric hydrogels promote CO2 hydrate formation kinetics
T2 - An experimental study
AU - Zhang, Yuxuan
AU - Thanusing, Moki
AU - Rahaman, Md Saifur
AU - Wang, Fei
AU - Alexander, Katia
AU - Connal, Luke A.
AU - Zhang, Fengyuan
AU - Wang, Xiaolin
N1 - © 2025 The Author(s)
PY - 2025/9/15
Y1 - 2025/9/15
N2 - Hydrogels are appealing support structures for the promotion of clathrate hydrate by increasing the gas–liquid contact surface area. However, due to their soft and adhesive nature, the current hydrogel materials cannot independently support the formation of hydrates. In this work, we used free radical polymerisation to develop a set of hydrogels with varied functionality and density, and investigated the effect of hydrogel composition on its reusability and ability to promote CO2 hydrate formation kinetics. The hydrogels demonstrate better recyclability than those reported in literature and the sample with the composition methacrylic acid: [2-(methacryloyloxy) ethyl] trimethylammonium chloride:ethylene glycol dimethacrylate = 47.5:47.5:5 exhibits optimal performance, with a normalised CO2 hydrate growth rate during the initial 30 min (NR30) of 187.23 mol m−3 min−1, and an 8-hour water-to-hydrate conversion rate (CR8h) of 86.3 %. This study demonstrates the ability for molecular engineering of the hydrogel structure to enhance gas hydrate formation kinetics for the practical realization of hydrate-based carbon capture technology.
AB - Hydrogels are appealing support structures for the promotion of clathrate hydrate by increasing the gas–liquid contact surface area. However, due to their soft and adhesive nature, the current hydrogel materials cannot independently support the formation of hydrates. In this work, we used free radical polymerisation to develop a set of hydrogels with varied functionality and density, and investigated the effect of hydrogel composition on its reusability and ability to promote CO2 hydrate formation kinetics. The hydrogels demonstrate better recyclability than those reported in literature and the sample with the composition methacrylic acid: [2-(methacryloyloxy) ethyl] trimethylammonium chloride:ethylene glycol dimethacrylate = 47.5:47.5:5 exhibits optimal performance, with a normalised CO2 hydrate growth rate during the initial 30 min (NR30) of 187.23 mol m−3 min−1, and an 8-hour water-to-hydrate conversion rate (CR8h) of 86.3 %. This study demonstrates the ability for molecular engineering of the hydrogel structure to enhance gas hydrate formation kinetics for the practical realization of hydrate-based carbon capture technology.
KW - CO gas hydrate
KW - Hydrate formation kinetics
KW - Hydrate-based carbon capture
KW - Polymeric superabsorbent hydrogel
UR - http://www.scopus.com/inward/record.url?scp=105002158038&partnerID=8YFLogxK
U2 - 10.1016/j.fuel.2025.135329
DO - 10.1016/j.fuel.2025.135329
M3 - Article
AN - SCOPUS:105002158038
SN - 0016-2361
VL - 396
SP - 1
EP - 13
JO - Fuel
JF - Fuel
M1 - 135329
ER -