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AbstractA nanofoam drainage agent was developed to address the challenges of inadequate foam stability and foaming efficiency in the gas recovery process of foam drainage. The formulation of the primary foam drainage agent was obtained by screening and combining conventional anionic and amphoteric surfactants. Experimental results revealed a synergistic interaction between α-olefin sulfonate (AOS) and lauramidopropyl betaine (LAB-35). Specifically, when a mixture of 0.4 wt.% AOS and 0.1 wt.% LAB-35 was used, the surface tension of the primary foam drainage agent was measured to be 23.32 mN/m. Furthermore, modification of Fe3O4 nanoparticles with the silane coupling agent γ-(methacryloxy)propyl trimethoxysilane (KH-570) was performed to improve the dispersibility in aqueous solutions and enhance foam stability. The results of infrared spectroscopy, x-ray diffraction, thermogravimetric analysis, and contact angle measurements revealed the effective bonding of KH-570 to the surface of Fe3O4 nanoparticles. Additionally, the particle size distribution in the aqueous solution showed the excellent dispersion of the modified Fe3O4 nanoparticles. Through the incorporation of the modified Fe3O4 nanoparticles into the primary foam drainage agent, a nanofoam drainage agent with a half-life of 989 ± 6.5 s was developed. Microscopic observations of foam coarsening behavior revealed the mechanism behind foam stability. Performance testing of the foam drainage agent demonstrated the agent’s outstanding resistance against salinity, temperature, and oil and its remarkable liquid-carrying capacity. [ABSTRACT FROM AUTHOR]

This work used aqueous solution free radical polymerization to create polymers of 2‐acrylamide‐2‐methylpropane sulfonic acid, itaconic acid, and allyl polyoxyethylene ether as a high‐temperature resistant retarder (APMS/IA/APEG, from now on referred to as AIA). Gel permeation chromatography, fourier transform infrared (FTIR), proton nuclear magnetic resonance (1HNMR), and thermo‐gravimetric analysis (TG) were used to characterize their molecular structure and characteristics. Tests were conducted on the thickening time, rheological characteristics, and compressive strength of AIA in cement slurries. The cement slurry thickened for 276 min at 180°C during the test, and the cement stone's 24‐h compressive strength was consistently more than 20 MPa. The hydration products were analyzed using x‐ray diffractometer and scanning electron microscopy methods, which were then coupled with molecular dynamics simulations to elucidate the AIA retarding mechanism. When AIA is added to a cement slurry, it forms a chelate structure with Ca2+ and a strong adsorption layer on the surfaces of the cement particles. This stops the cement from hydrating. The AIA side chain, APEG, can wrap the active group in AIA at low temperatures. AIA exposes more adsorption groups because of the APEG chains stretching at higher temperatures. AIA can, therefore, be used for deep well operations at high temperatures. [ABSTRACT FROM AUTHOR]