The CO2 and Sodium Dodecyl Sulfate (SDS) assisted steam flooding technology was an effective approach addressed the persistent issues that have hindered the stable development of high-viscosity cold oil through steam injection. However, in the process of steam flow through porous media, the synergistic influence of the oil film adsorbed in near wellbore porous media, and the CO2-SDS on steam heat transfer has not been investigated. Steam heat transfer is the key factors affecting heavy oil recovery. The primary objective of this study was to research the effect of CO2-SDS on steam heat transfer and oil film stripping by designing experiments. The study results demonstrated that in the initial stage of displacement, the heat transfer resistance between the steam and the porous medium was increased by the oil film adsorbed in near wellbore area. In additional, the condensation mode of the steam was altered from bead condensing to film condensing by the composite thermal fluid flooding, preventing the steam heat dissipation near wellbore area and transferring more thermal to the long-distance area. At the later stage of displacement, the interfacial tension between oil-water and oil-gas was reduced by CO2-SDS, improving the fluidity of oil and providing the seepage channel for steam, and increasing the steam thermal sweep range. Compared to the sandpack experiment of steam flooding, the temperature at the output end of the sandpack model increased from 69.8 °C to 88.7 °C, indicating an expansion of the steam heat sweep range and successful long-distance heat transfer during composite thermal fluid flooding. In the process of composite thermal fluid flooding, the maximum displacement pressure difference increased from 2.28 MPa to 3.07 MPa, and the maximum oil recovery rate increased from 2.48 g/mL to 2.81 g/mL. The peak of the high production period was raised, resulting in a 40.97% to 51.86% increase in recovery rates.
ron/chromium hydroxide coprecipitation controls the fate and transport of toxic chromium (Cr) in many natural and engineered systems. Organic coatings on soil and engineered surfaces are ubiquitous; however, mechanistic controls of these organic coatings over Fe/Cr hydroxide coprecipitation are poorly understood. Here, Fe/Cr hydroxide coprecipitation was conducted on model organic coatings of humic acid (HA), sodium alginate (SA), and bovine serum albumin (BSA). The organics bonded with SiO2 through ligand exchange with carboxyl (–COOH), and the adsorbed amounts and pKa values of –COOH controlled surface charges of coatings. The adsorbed organic films also had different complexation capacities with Fe/Cr ions and Fe/Cr hydroxide particles, resulting in significant differences in both the amount (on HA > SA(–COOH) ≫ BSA(–NH2)) and composition (Cr/Fe molar ratio: on BSA(–NH2) ≫ HA > SA(–COOH)) of heterogeneous precipitates. Negatively charged –COOH attracted more Fe ions and oligomers of hydrolyzed Fe/Cr species and subsequently promoted heterogeneous precipitation of Fe/Cr hydroxide nanoparticles. Organic coatings containing –NH2 were positively charged at acidic pH because of the high pKa value of the functional group, limiting cation adsorption and formation of coprecipitates. Meanwhile, the higher local pH near the –NH2 coatings promoted the formation of Cr(OH)3. This study advances fundamental understanding of heterogeneous Fe/Cr hydroxide coprecipitation on organics, which is essential for successful Cr remediation and removal in both natural and engineered settings, as well as the synthesis of Cr-doped iron (oxy)hydroxides for material applications.