Microemulsions surfactant-polymer systems

Description of the different mimetic systems will be the starting point of the presentation (Sect. 2). Preparation and characterization of monolayers (Langmuir films), Langmuir-Blodgett (LB) films, self-assembled (SA) mono-layers and multilayers, aqueous micelles, reversed micelles, microemulsions, surfactant vesicles, polymerized vesicles, polymeric vesicles, tubules, rods and related SA structures, bilayer lipid membranes (BLMs), cast multibilayers, polymers, polymeric membranes, and other systems will be delineated in sufficient detail to enable the neophyte to utilize these systems. Ample references will be provided to primary and secondary sources. 

The goals of this work have been to determine the effect of polymers on the phase behavior of aqueous surfactant solutions, prior to and after equilibration with oil, to understand the mechanism of the so-called "surfactant-polymer interactions (SPI) in EOR, to develop a simple model which will predict the salient features of the phase behavior in polymer-microeraulsion systems, and to test the concept of using sulfonate-carboxylate mixed microemulsions for increased salt tolerance. 

The effect of polymers on microemulsions phase behavior has been reported by Hesselink and Faber (8). They have described the surfactant-polymer phase separation in terras of the incompatibility of two different polymers in a single solvent, considering the microemulsion as a pseudo-polymer system. The effect of polymers on the phase behavior of micellar fluids has been recently studied by Pope et al. (9) and others (10,11). 

Surfactants have been designed to lower y in C02-based systems. The first generation of research involving surfactants in SCFs addressed water-in-oil (W/O) microemulsions and polymer latexes in ethane and propane, as reviewed elsewhere. (43-45). This work provided a foundation for studies in CO2, which has weaker van der Waals forces (a/v) than ethane. Surfactants with both C02-philic and C02-phobic segments have been used to form microemulsions, emulsions, and organic polymer latexes in CO2. 

FIGURE 9.3 Interfacial tensions and solubilization parameters for microemulsions in a system containing a synthetic petroleum sulfonate, an alcohol cosurfactant, a mixture of refined oils, and NaCl brine. (From Reed, R.L. and Healy, R.N., in Improved Oil Recovery by Surfactant and Polymer Flooding, Shah, D.O. and Schechter, R.S., Eds., Academic Press, New York, 1977. With permission.)... 

There are basically two topics that need to be addressed regarding the effect of amphiphilic polymers on the physical behaviour of microemulsions. The first topic is related to phase behaviour and structure formation. Amphiphilic polymers can strongly influence phase behaviour because of their impact on the bending rigidity of the surfactant film. For both droplet micro emulsions and bicontinuous microemulsions such phenomena were studied. Especially in droplet microemulsions, amphiphilic polymers were used to interconnect microemulsion domains. This leads to ordering phenomena and can alter the phase behaviour. The second topic again is based on systems where microemulsion domains are connected via polymers. It covers dynamic phenomena with a focus on viscoelastic properties. Important in this area is the formation of transient or permanent networks. 

The proceedings cover six major areas of research related to chemical flooding processes for enhanced oil recovery, namely, 1) Fundamental aspects of the oil displacement process, 2) Microstructure of surfactant systems, 3) Emulsion rheology and oil displacement mechanisms, 4) Wettability and oil displacement mechanisms, 5) Adsorption, clays and chemical loss mechanisms, and 6) Polymer rheology and surfactant-polymer interactions. This book also includes two invited review papers, namely, "Research on Enhanced Oil Recovery Past, Present and Future," and "Formation and Properties of Micelles and Microemulsions" by Professor J. J. Taber and Professor H. F. Eicke respectively. 

There are two additional types of chemical flooding systems that involve surfactants which are briefly mentioned here. One of these systems utilizes surfactant-polymer mixtures. One such study was presented by Osterloh et al. [72] which examined anionic PO/EO surfactant microemulsions containing polyethylene glycol additives adsorbed onto clay. The second type of chemical flood involves the use of sodium bicarbonate. The aim of the research was to demonstrate that the effectiveness of sodium bicarbonate in oil recovery could be enhanced with the addition of surfactant. The surfactant adsorption was conducted in batch studies using kaolinite and Berea sandstone [73]. It was determined that the presence of a low concentration of surfactant was effective in maintaining the alkalinity even after long exposures to reservoir minerals. Also, the presence of the sodium bicarbonate is capable of reducing surfactant adsorption. 

Nanocapsules act like a reservoir, which are called vesicular systems. They carry the active substance entrapped in the solid polymeric membrane or on their surfaces. The cavily inside contains either oil or water. A schematic diagram of Polymer Nanocapsules is shown in Fig. 9.2 [5], There are different methods that are used nowadays to prepare polymeric nanoparticles, such as nanoprecipitation (also termed as the solvent diffusion and solvent displacement method), solvent evaporation, dialysis, microemulsion, surfactant-free emulsion, salling-out, supercritical fluid technology, and interfacial polymerization [2]. Among these methods, nanoprecipitation is a fast and simple process, which does not require a pre-prepared polymer emulsion before the nanoparticle preparation. It produces a dispersion of nanoparticles by precipitation of preformed hydrophobic polymer solution. Under... 

One parameter that has been discovered to be crucially important in the successful implementation of the surfactant-polymer flooding process is the salinity of the aqueous phase. As discussed previously, addition of salt to the microemulsion system induces the change from lower- to middle- to upper-phase microemulsion (Fig. 15) [33]. It was found that at a particular salt concentration, deemed the optimal salinity, a number of important parameters were optimized for the oil recovery process. The optimal salinity was found to occur when equal amounts of oil and brine were solubilized by the middle-phase microemulsion [50]. 

The temperature (or salinity) at which optimal temperature (or optimal salinity), because at that temperature (or salinity) the oil—water interfacial tension is a minimum, which is optimum for oil recovery. For historical reasons, the optimal temperature is also known as the HLB (hydrophilic—lipophilic balance) temperature (42,43) or phase inversion temperature (PIT) (44). For most systems, all three tensions are very low for Tlc < T < Tuc, and the tensions of the middle-phase microemulsion with the other two phases can be in the range 10 5—10 7 N/m. These values are about three orders of magnitude smaller than the interfacial tensions produced by nonmicroemulsion surfactant solutions near the critical micelle concentration. Indeed, it is this huge reduction of interfacial tension which makes micellar-polymer EOR and its SEAR counterpart physically possible. 

Single-step preparations of composite polymers have been examined in previous sections. The volume fraction of the continuous phase was, however, relatively small in those cases. In contrast, the present method allows us to prepare composites with larger volume fractions of the continuous phase. Composites with large volume fractions of the continuous phase can also be obtained in a single-step by polymerizing an emulsion or a microemulsion [24]. An emulsion of a hydrophobic (hydrophilic) monomer in another hydrophilic (hydrophobic) monomer can be extremely stable (even thermodynamically stable, and then it is called a microemulsion) if a sufficiently large amount of surfactant is introduced into the system. For an emulsion to be thermodynamically stable, a cosurfactant is in most cases needed besides the surfactant. The latter method was used to prepare composites by employing acrylamide... 

Abstract This review describes how the unique nanostructures of water-in-oU (W/0), oil-in-water (0/W) and bicontinuous microemulsions have been used for the syntheses of some organic and inorganic nanomaterials. Polymer nanoparticles of diameter approximately 10-50 nm can easily be obtained, not only from the polymerization of monomers in all three types of microemulsions, but also from aWinsor l-like system. A Winsor 1-like system with a semi-continuous process can be used to produce microlatexes with high weight ratios of polymer to surfactant (up to 25). On the other hand, to form inorganic nanoparticles, it is best to carry out the appropriate chemical reactions in W/0- and bicontinuous microemulsions. 

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