Browsing by Author "ShamsiJazeyi, Hadi"
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Item Advanced Applications of Polymers for Enhanced Oil Recovery(2014-11-06) ShamsiJazeyi, Hadi; Hirasaki, George J; Verduzco, Rafael; Tour, James; Biswal, LisaWith the increasing global demand for crude oil, it is essential to increase the oil production in economic ways. This requires a significant increase in application of advanced technologies in this area. Enhanced Oil Recovery (EOR) processes are known as series of different advanced technologies, which can be used to increase the oil production from a given oil reservoir. The traditional use of polymers in EOR is almost limited to increasing viscosity of the aqueous fluids injected into the reservoir. By increasing the viscosity of the injected fluids, more areas of the reservoir can be swept, and therefore more oil is expected to be recovered. In this thesis proposal, a number of advanced polymer applications for EOR are investigated. Polymers are known as a very promising class of materials with wide range of properties, especially combined with other advanced materials, such as nanoparticles. Therefore, there is a huge potential for developing new application of polymers in EOR processes. The first application introduced in this thesis is to use polymers as sacrificial adsorption agents for anionic surfactants. In a subclass of EOR, known as chemical EOR, surfactants are injected to lower the interfacial tension of oil and brine, resulting in recovery of more oil. However, one of the challenges facing these processes is the adsorption of surfactants onto the reservoir rock, which requires excessive injection of surfactant to compensate for the adsorption. This significantly increases the cost of the chemical EOR to values much more than what is actually needed for oil recovery. In second chapter of this thesis, sodium polyacrylate is introduced as a sacrificial adsorption agent, a chemical that is injected to decrease the adsorption of anionic surfactant. The results show that the material cost of chemical EOR can be reduced by up to 80% in case of using polyacrylate as a sacrificial agent for anionic surfactants. In addition, application of polyacrylate as a sacrificial agent for zwitterionic surfactants was investigated. In spite the significant reduction seen in the adsorption of anionic surfactants once polyacrylate is used, adsorption of zwitterionic surfactants is only slightly reduced after adding polyacrylate. In order to understand the reasons behind this dismal reduction, the effect of pH on adsorption of lauryl betaine (as the zwitterionic surfactant in this study) is studied. Based on the experimental data, a hypothetic mechanism is introduced to explain the adsorption properties of betaine. This hypothetic mechanism also explains why polyacrylate shows a very slight reduction in adsorption of zwitterionic surfactants while it significantly reduces adsorption of anionic surfactants. Finally, the effect of polymer coating on interfacial properties of nanoparticles in the absence or presence of surfactants is studied. Interfacial properties of polymer-coated nanoparticles in EOR have been traditionally limited to only emulsions (Pickering Emulsions). In this thesis, we have provided experimental evidence that polymer-coated nanoparticles can migrate to micro-emulsion phases even in the absence of emulsions. Some of these polymer-coated nanoparticles are dispersed in aqueous solutions, but they will precipitate in the micro-emulsion phase once mixed with the oil. This observation by itself can be used in EOR applications through understanding the fact that aqueous stability of nanoparticles is not the sufficient condition for nanoparticles to remain stable when injected into oil reservoirs. Many previous researchers have only focused on stability of nanoparticles in aqueous solutions as the only requirement for stability of nanoparticles even after injection into oil reservoir. This assumption is challenged based on our work in this thesis.Item Segregation of Amphiphilic Polymer-Coated Nanoparticles to Bicontinuous Oil/Water Microemulsion Phases(American Chemical Society, 2017) Qi, Luqing; ShamsiJazeyi, Hadi; Ruan, Gedeng; Mann, Jason A.; Lin, Yen-Hao; Song, Chen; Ma, Yichuan; Wang, Le; Tour, James M.; Hirasaki, George J.; Verduzco, RafaelPolymer-coated nanoparticles are interfacially active and have been shown to stabilize macroscopic emulsions of oil and water, also known as Pickering emulsions. However, prior work has not explored the phase behavior of amphiphilic nanoparticles in the presence of bicontinuous microemulsions. Here, we show that properly designed amphiphilic polymer-coated nanoparticles spontaneously and preferentially segregate to the bicontinuous microemulsion phases of oil, water, and surfactant. Mixtures of hydrophilic and hydrophobic chains are covalently grafted onto the surface of oxidized carbon black nanoparticles. By sulfating hydrophilic chains, the polymer-coated nanoparticles are stable in the aqueous phase at salinities up to 15 wt % NaCl. These amphiphilic, negatively charged polymer-coated nanoparticles segregate to the bicontinuous microemulsion phases. We analyzed the equilibrium phase behavior of the nanoparticles, measured the interfacial tension, and quantified the domain spacing in the presence of nanoparticles. This work shows a novel route to the design of polymer-coated nanoparticles which are stable at high salinities and preferentially segregate to bicontinuous microemulsion phases.Item Thermoresponsive PNIPAAM bottlebrush polymers with tailored side-chain length and end-group structure(The Royal Society of Chemistry, 2014) Li, Xianyu; ShamsiJazeyi, Hadi; Pesek, Stacy L.; Agrawal, Aditya; Hammouda, Boualem; Verduzco, RafaelWe explore the phase behaviour, solution conformation, and interfacial properties of bottlebrush polymers with side-chains comprised of poly(N-isopropylacrylamide) (PNIPAAM), a thermally responsive polymer that exhibits a lower critical solution temperature (LCST) in water. PNIPAAM bottlebrush polymers with controlled side-chain length and side-chain end-group structure are prepared using a ﾓgrafting-throughﾔ technique. Due to reduced flexibility of bottlebrush polymer side-chains, side-chain end-groups have a disproportionate effect on bottlebrush polymer solubility and phase behaviour. Bottlebrush polymers with a hydrophobic end-group have poor water solubilities and depressed LCSTs, whereas bottlebrush polymers with thiol-terminated side-chains are fully water-soluble and exhibit an LCST greater than that of PNIPAAM homopolymers. The temperature-dependent solution conformation of PNIPAAM bottlebrush polymers in D2O is analyzed by small-angle neutron scattering (SANS), and data analysis using the Guinier-Porod model shows that the bottlebrush polymer radius decreases as the temperature increases towards the LCST for PNIPAAM bottlebrush polymers with relatively long 9 kg mol1 sidechains. Above the LCST, PNIPAAM bottlebrush polymers can form a lyotropic liquid crystal phase in water. Interfacial tension measurements show that bottlebrush polymers reduce the interfacial tension between chloroform and water to levels comparable to PNIPAAM homopolymers without the formation of microemulsions, suggesting that bottlebrush polymers are unable to stabilize highly curved interfaces. These results demonstrate that bottlebrush polymer side-chain length and flexibility impact phase behavior, solubility, and interfacial properties.