During oil displacement,surfactants often encounter challenges such as emulsion instability and channeling,which can compromise their efficiency.To address these issues,polymer microspheres were synthesized via revers...During oil displacement,surfactants often encounter challenges such as emulsion instability and channeling,which can compromise their efficiency.To address these issues,polymer microspheres were synthesized via reverse microemulsion polymerization using acrylamide,2-methyl-2-acrylamidopropane sulfonic acid,and stearyl methacrylate as monomers,with N,N-methylenebisacrylamide as the crosslinker.The microspheres were then combined with sodium alkyl alcohol polyoxyethylene ether carboxylate to enhance emulsion stability and expand the swept volume of surfactant.A stable reverse microemulsion system was prepared using the maximum water solubilization rate as the indicator,and microspheres were synthesized based on this system.The ability of the microspheres to enhance emulsion stability was systematically evaluated.The plugging performance and enhanced oil recovery(EOR)efficiency of the microsphere/surfactant composite system were assessed through core seepage and oil displacement experiments.The experimental results demonstrated that microspheres were successfully prepared in a water-in-oil reverse microemulsion system with a solubilization rate of 42%.The emulsion stability was evaluated under an oil-to-water ratio of 7:3,a temperature of 80℃,and a salinity of 44,592 mg/L,by manually shaking the test tube five times.It was observed that the complete phase separation time of the emulsion increased from 10 to 120 min after the addition of microspheres.Under different permeability conditions(100×10^(-3),300×10^(-3),500×10^(-3)μm^(2)),the recovery efficiency of the composite system increased by 4.5%,8.3%,and 4.8%,respectively,compared to a single surfactant system.The microspheres developed in this study enhanced emulsion stability and increased the swept volume of surfactant within the formation,significantly boosting its oil recovery efficiency.展开更多
Nanohydrogels from inverse microemulsion (w/o) polymerization, at 25°C, of N-isopropylacrylamide (NIPA) and functionalized monomers are described. The functionalized monomers were: N-(pyridine-4-ylmethyl) acrylam...Nanohydrogels from inverse microemulsion (w/o) polymerization, at 25°C, of N-isopropylacrylamide (NIPA) and functionalized monomers are described. The functionalized monomers were: N-(pyridine-4-ylmethyl) acrylamide (NP4MAM) and tert-butyl 2-acrylamidoethyl carbamate (2AAECM). The polymeric nanohydrogel obtained was characterized by attenuated total reflectance Fourier-transformed infrared spectroscopy (ATR-FTIR) and proton nuclear magnetic resonance spectrometry (1HNMR), while their morphology and particle size was assessed by scanning electron microscopy (SEM) and dynamic light scattering. Their thermal properties were studied by Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA). As a preliminary measure of biocompatibility, in vitro evaluations of the nanohydrogels were carried out by cellular toxicity (colon carcinoma cells, CT-26) and hemocompatibility tests. These evaluations showed that these nanohydrogels were not toxic in the examined concentration range and exhibited preliminary blood compatibility;therefore they could be used in biomedical applications.展开更多
基金supported by the Natural Science Foundation of Shandong Province(ZR2021ME007)the National Natural Science Foundation in China(51574267)the Key Projects of China National Key Research and Development Plan(2019YFA0708703)。
文摘During oil displacement,surfactants often encounter challenges such as emulsion instability and channeling,which can compromise their efficiency.To address these issues,polymer microspheres were synthesized via reverse microemulsion polymerization using acrylamide,2-methyl-2-acrylamidopropane sulfonic acid,and stearyl methacrylate as monomers,with N,N-methylenebisacrylamide as the crosslinker.The microspheres were then combined with sodium alkyl alcohol polyoxyethylene ether carboxylate to enhance emulsion stability and expand the swept volume of surfactant.A stable reverse microemulsion system was prepared using the maximum water solubilization rate as the indicator,and microspheres were synthesized based on this system.The ability of the microspheres to enhance emulsion stability was systematically evaluated.The plugging performance and enhanced oil recovery(EOR)efficiency of the microsphere/surfactant composite system were assessed through core seepage and oil displacement experiments.The experimental results demonstrated that microspheres were successfully prepared in a water-in-oil reverse microemulsion system with a solubilization rate of 42%.The emulsion stability was evaluated under an oil-to-water ratio of 7:3,a temperature of 80℃,and a salinity of 44,592 mg/L,by manually shaking the test tube five times.It was observed that the complete phase separation time of the emulsion increased from 10 to 120 min after the addition of microspheres.Under different permeability conditions(100×10^(-3),300×10^(-3),500×10^(-3)μm^(2)),the recovery efficiency of the composite system increased by 4.5%,8.3%,and 4.8%,respectively,compared to a single surfactant system.The microspheres developed in this study enhanced emulsion stability and increased the swept volume of surfactant within the formation,significantly boosting its oil recovery efficiency.
基金Financial support for this work from Ministerio de Ciencia y Tecnologia is gratefully acknowledged(MICINN).
文摘Nanohydrogels from inverse microemulsion (w/o) polymerization, at 25°C, of N-isopropylacrylamide (NIPA) and functionalized monomers are described. The functionalized monomers were: N-(pyridine-4-ylmethyl) acrylamide (NP4MAM) and tert-butyl 2-acrylamidoethyl carbamate (2AAECM). The polymeric nanohydrogel obtained was characterized by attenuated total reflectance Fourier-transformed infrared spectroscopy (ATR-FTIR) and proton nuclear magnetic resonance spectrometry (1HNMR), while their morphology and particle size was assessed by scanning electron microscopy (SEM) and dynamic light scattering. Their thermal properties were studied by Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA). As a preliminary measure of biocompatibility, in vitro evaluations of the nanohydrogels were carried out by cellular toxicity (colon carcinoma cells, CT-26) and hemocompatibility tests. These evaluations showed that these nanohydrogels were not toxic in the examined concentration range and exhibited preliminary blood compatibility;therefore they could be used in biomedical applications.
