Hydrate-based CO2 sequestration beneath oceanic sediments is an emerging technique that involves the injection of CO2 into the hydrate stability zone (HSZ) beneath the seabed, forming hydrate cap that structurally traps the injected CO2 and reduces the risk of leaking CO2 from the storage sediment. Gas hydrates are adequately stable in sand sediments saturated with fresh water; however, the salinity of oceanic water impairs hydrate formation kinetics, stability, and CO2 storage capacity. In addition to sandstones, marine sediments are composed of many clay minerals that could affect hydrate formation. Therefore, this study experimentally simulates CO2 injection into sand and clayey sand sediments to assess the potential of CO2 hydrate formation. CO2 hydrates are formed inside a high-pressure reactor, which contains unconsolidated sediment bed/pack (silica sand; mixed sand with bentonite clay: 5 wt% and 10 wt%), saturated with de-ionized water or brine (3.3 wt% NaCl). Hydrate formation experiments were performed at 4 MPa pressure and 274.15 K temperature. Results show that CO2 hydrate formed within the sand sediment, with induction times of 6 and 8.5 h, for the de-ionized and brine systems, respectively. CO2 gas mole uptake in the de-ionized system was 71.54 mmol/mol however, in the brine system the gas uptake was 56.95 mmol/mol. Hence this 20.4% reduction in the gas uptake indicated the inhibition effect of salinity. In contrast, in the brine-saturated 5 wt% clay-sand sediment, the induction time was 6.5 h, indicating the promoting effect of the nano-sized clay particles. However, the gas uptake in this brine-saturated clay-sand sediment was reduced by 45.51% compared to the brine-saturated sand sediment. Increasing the clay content to 10 wt% prevented CO2 hydrate formation due to porosity reduction. Moreover, de-ionized water in clayey sand sediments prevented hydrate formation due to clay swelling. Finally, CO2 hydrate formation at the end of each experiment was visually confirmed.