The water-soluble polymer PAM (polyacrylamide) is used in enhanced oil recovery (EOR) operations. It is pumped into water injection wells to increase the viscosity of the injected water and in turn to direct more oil towards production wells. This EOR process is proven to be sensitive to operational well conditions such as hydrocarbon reservoir temperature, as well as the salinity of the injected water and/or formation water. These operational conditions lead to technical challenges ranging from the solubility of PAM in injection water to the behaviour of PAM inside the reservoir. To gain a clear picture of the functionality of PAM in EOR applications, this report characterizes its behaviour of in terms of degree of hydrolysis and changes in solution viscosity determined using Perkin Elmer spectrum 100 Fourier transform infrared-Attenuated total reflection (FTIR)-ATR and nuclear magnetic resonance spectroscopy (¹H NMR) and a Fann model 35 Couette and Cole Parmer rotational viscometer, respectively. Different shear rates were investigated to determine the effect of shear on PAM gel stability. Experiments were performed for PAM mixed with formation brine at 50, 70, and 90 °C for ageing times of up to 30 days. The results indicate that the degree of hydrolysis achieved after 30 days is much higher in saline solutions than in pure water, and that this effect is more pronounced at higher temperatures. For example, after 30 days at 50 °C, the hydrolysis level was observed to be 53%, rising to 65% at 70 °C and 75% at 90 °C in PAM mixed with brines. Similar trends were observed with viscosity, where lower viscosity was observed for samples at higher temperatures and salinities. It is thus reasonable to conclude that the degree of hydrolysis causes changes in the viscosity of the polymer gel, leading to a decline in its performance as it ages.

Steel slag is a by-product of steelmaking which has emerged as a potential CO₂ sequestration material due to its high reactivity and abundance. This research investigates the use of steel slag waste for the direct capture of carbon from air and its storage through mineral carbonation. Two abundant wastes, blast-furnace slag (BFS) and ladle slag (LS), were tested for their carbon sequestration potential, and the effects of operational parameters such as reaction time between CO₂ and slag waste, temperature, liquid-solid ratio, and pressure on CO₂ sequestration were determined. Quantitative and qualitative results reveal that much higher CO₂ sequestration was achieved using LS compared to BFS after exposure to CO₂ for 1 day at room temperature. By increasing the exposure time to four days, levels of CO₂ sequestration increased gradually from 2.71% to 4.19% and 23.46%-28.21% for BFS and LS respectively. Increasing the temperature from 20 ± 2 °C to 90 ± 2 °C positively influenced CO₂ sequestration in BFS, resulting in an enhancement from 3.45% to 13.21%. However, the impact on LS was insignificant, with sequestration levels rising from 27.72% to 29.90%. Moreover, better CO₂ sequestration was observed for BFS than LS when the liquid-to-solid ratio increased from 3:1 to 4:1, whereupon the sequestration potential reached approximately 15% for BFS and 30% for LS at 90 ± 2 °C. Meanwhile, higher pressure reduced the sequestration potential of slag. The results of this study suggest that there is potential for scaling up the process to industrial applications and contributing to the reduction of CO₂ emissions in the steelmaking industry.