To enhance oil and gas recovery, a novel hydrophobic terpolymer was synthesized via free radical polymerization. The terpolymer consists of acrylamide, acrylic acid, and hydrophobic monomers, and is used as a hydraulic fracturing fluid thickener for freshwater environments. Hydrophobic groups were introduced into terpolymer to improve its tackiness and temperature resistance. The conformation and key parameters of hydrophobic monomers at different temperatures were investigated through a combination of experiments and molecular dynamics simulations. These methods were employed to elucidate the mechanism behind its high-temperature resistance. The experiment results show that, at concentrations between 0.2% and 0.4%, significant intermolecular aggregation occurs, leading to a substantial increase in solution viscosity. Configuring the base fluid of synthetic polymer fracturing fluid with 1% doping, the apparent viscosities of the base fluid were 129.23 mPa·s and 133.11 mPa·s, respectively. The viscosity increase rate was 97%. The base fluid was crosslinked with 1.5% organozirconium crosslinker to form a gel. The controlled loss coefficient and loss velocity of the filter cake were C₃ = 0.84 × 10⁻³ m/min^1/2 and v_c = 1.40 × 10⁻⁴ m/min at 90 °C, meeting the technical requirements for water-based fracturing fluid. Molecular dynamics simulations revealed that the radius of gyration of the hydrophobically linked polymer chain segments decreases as the temperature increases. This is due to the increased thermal motion of the polymer chain segments, resulting in less stretching and intertwining of the chains. As a result, the polymer chains move more freely, which decreases the viscosity of the solution. In conclusion, the proposed fracturing fluid thickener system demonstrates excellent overall performance and shows significant potential for application in oil and gas recovery.

Addressing the inherent brittleness of cement to mitigate infrastructure failures stemming from cracking is imperative. To accomplish both early crack resistance and subsequent self-healing capabilities, a biomimetic microstructure composed of a sodium polyacrylate (CSPA) network interwoven with hydration products was developed. The calcium-enriched polymer network formed via in situ polymerization of sodium acrylate (ANa) can enhance the mechanical properties of cement and achieve efficient self-healing of cracks. The porous structure of sodium polyacrylate (PANa) formed in pore solution at room temperature to simulate cement hydration conditions was observed by scanning electron microscopy (SEM). Feature peaks found by Fourier transform infrared (FTIR) spectroscopy as well as confocal Raman microscopy (CRM) suggested that ANa was polymerized successfully. Notably, CSPA samples demonstrated a remarkable 104% increase in flexural strength, attributed to the efficient transmission and dissipation of external forces along the polymer network embedded within the cement matrix. Additionally, after a 28-day hydration, CSPA specimens exhibited enhanced compressive strength compared to blank cement samples. This enhancement stems from the formation of a uniform polymer network, which effectively decreased the porosity and densified the microstructure of cement. Moreover, this organic–inorganic hybrid structure contributes to efficient crack healing, as the calcium-rich polymer network binds calcium ions and promotes the generation of healing products. The healing products consist of calcium hydroxide (CH), CaCO₃ (aragonite), C-S-H (calcium–silicate–hydrate), and PANa.