In industry, silica nanoparticles (NPs) are obtained by the fuming and the precipitation method. Fumed silica NPs are commonly used in the preparation of nanocomposites because they have an extremely low bulk density (160–190 kg/m³), large surface area (50–600 m²/g), and nonporous surface, which promotes strong physical contact between the NPs and the organic phase. Fumed silica has fewer silanol groups (Si–OH) on its surface than the silica prepared by the Stöber method. However, the number of –OH groups on the fumed silica surface can be increased by pretreating them with sodium hydroxide (NaOH) before further surface modification. In this study, the effectiveness of the NaOH pretreatment was evaluated on commercial fumed silica NPs with a surface area of 200 m²/g. The number of surface –OH groups was estimated by potentiometric titration. The pretreated fumed NPs, and the precipitated NPs (prepared by the Stöber method) were modified with 3-aminopropyltriethoxysilane (APTES) to obtain A200S and nSiO₂-APTES, respectively. The NPs were characterized using electron dispersive scanning (EDS), scanning electron microscopy (SEM), dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), BET (Brunauer–Emmett–Teller) analysis, and ζ-potential. XRD confirmed the presence of the organo-functional group on the surface of both NPs. After the amino-functionalization, the ζ-potential values of the nSiO₂ and A200 changed from −35.5 mV and −14.4 mV to +26.2 mV and +11.76 mV, respectively. Consequently, we have successfully synthesized functionalized NPs with interesting, specific surface area and porosity (pore volume and size), which can be attractive materials for chemical and energy industries.

In this study, a set of advanced characterization techniques were used to evaluate the morphological, structural, and thermal properties of a novel molecular hybrid based on silica nanoparticles/hydrolyzed polyacrylamide (CSNH-PC1), which was efficiently obtained using a two-step synthetic pathway. The morphology of the nanohybrid CSNH-PC1 was determined using scanning electron microscopy (SEM), dynamic light scattering (DLS), and nanotracking analysis (NTA) techniques. The presence of C, N, O, and Si atoms in the nanohybrid structure was verified using electron dispersive scanning (EDS). Moreover, the corresponding structural analysis was complemented using powder X-ray diffraction (XRD) and attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FT-IR). The covalent bond between APTES-functionalized SiO₂ nanoparticles (nSiO₂-APTES), and the hydrolyzed polyacrylamide (HPAM) chain (MW ≈ 20.10⁶ Da) was confirmed with high-resolution X-ray spectroscopy (XPS). Finally, the thermal properties of the nanohybrid were evaluated by using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The results showed that the CSNH-PC1 has a spherical morphology, with sizes between 420–480 nm and higher thermal resistance compared to HPAM polymers without modification, with a glass transition temperature of 360 °C. The integration of these advanced characterization techniques implemented here shows promising results for the study and evaluation of new nanomaterials with multiple applications.

Viscosity losses and high degradation factors have a drastic impact over hydrolyzed polyacrylamides (HPAM) currently injected, impacting the oil recovery negatively. Previous studies have demonstrated that biopolymers are promising candidates in EOR applications due to high thermochemical stability in harsh environments. However, the dynamic behavior of a biopolymer as scleroglucan through sandstone under specific conditions for a heavy oil field with low salinity and high temperature has not yet been reported. This work presents the rock–fluid evaluation of the scleroglucan (SG at 935 mgL⁻¹) and sulfonated polyacrylamide (ATBS at 2500 mgL⁻¹) to enhance oil recovery in high-temperature for heavy oils (212 °F and total dissolved solid of 3800 mgL⁻¹) in synthetic (0.5 Darcy) and representative rock samples (from 2 to 5 Darcy) for a study case of a Colombian heavy oilfield. Dynamic evaluation at reservoir conditions presents a scenario with stable injectivity after 53.6 PV with a minimal pressure differential (less than 20 psi), inaccessible porous volume (IPV) of 18%, dynamic adsorption of 49 µg/g, and resistance and residual resistance factors of 6.17 and 2.84, respectively. In addition, higher oil displacement efficiency (up to 10%) was obtained with lower concentration (2.7 times) compared to a sulfonated polyacrylamide polymer.

Biopolymers emerge as promising candidates for enhanced oil recovery (EOR) applications due to their molecular structures, which exhibit better stability than polyacrylamides under harsh conditions. Nonetheless, biopolymers are susceptible to oxidation and biological degradation. Biopolymers reinforced with nanoparticles could be a potential solution to the issue. The nanofluids’ stability and performance depend on the nanoparticles’ properties and the preparation method. The primary objective of this study was to evaluate the effect of the preparation method and the nanoparticle type (SiO₂, Al₂O₃, and TiO₂) on the viscosity and stability of the scleroglucan (SG). The thickening effect of the SG solution was improved by adding all NPs due to the formation of three-dimensional structures between the NPs and the SG chains. The stability test showed that the SG + Al₂O₃ and SG + TiO₂ nanofluids are highly unstable, but the SG + SiO₂ nanofluids are highly stable (regardless of the preparation method). According to the ANOVA results, the preparation method and standing time influence the nanofluid viscosity with a statistical significance of 95%. On the contrary, the heating temperature and NP type are insignificant. Finally, the nanofluid with the best performance was 1000 ppm of SG + 100 ppm of SiO₂_120 NPs prepared by method II.

Polymer flooding represents the most common chemical enhanced oil recovery (CEOR) method used at commercial scale. In this process, the polymeric solutions (generally hydrolyzed polyacrylamide - HPAM) are injected to improve the oil/water mobility ratio (M). However, due to mechanical, chemical, bio, and thermal degradation, polymer viscosity losses can occur, causing a negative impact on oil sweep efficiency. In this case, biopolymers seem to be promising candidates in EOR applications with special structural characteristics, which result in excellent stability in harsh environments with high temperatures, ionic forces, and shear stresses. This paper presents the laboratory evaluation of Scleroglucan (SG) and a commercial sulfonated polyacrylamide (ATBS) in synthetic brine, representative of a Colombian heavy-oil field. The effects of ionic strength, pH, temperature, and shear degradation effects on polymer viscosity were also evaluated. For SG, the results reflect its tolerance to high salinities (0-5%wt), ionic strengths (Na+, K+, Ca2+, and Mg2+), shear rates (0-300,000 s-1), temperatures (30, 50, 80 and 100 °C), and pH variations (3-10). The biopolymer was capable of preserving its viscous properties and stability after of the effect of these variables. Finally, the target viscosity (set as 17 cp) was achieved with a lower concentration (2.7 times) than the ATBS polymer tested.