The tremendous interest in magnetic nanoparticles (MNPs) is reflected in published research that ranges from novel methods of synthesis of unique nanoparticle shapes and composite structures to a large number of MNP characterization techniques, and finally to their use in many biomedical and nanotechnology-based applications. The knowledge gained from this vast body of research can be made more useful if we organize the associated results to correlate key magnetic properties with the parameters that influence them. Tuning these properties of MNPs will allow us to tailor nanoparticles for specific applications, thus increasing their effectiveness. The complex magnetic behavior exhibited by MNPs is governed by many factors; these factors can either improve or adversely affect the desired magnetic properties. In this report, we have outlined a matrix of parameters that can be varied to tune the magnetic properties of nanoparticles. For practical utility, this review focuses on the effect of size, shape, composition, and shell-core structure on saturation magnetization, coercivity, blocking temperature, and relaxation time.

The current simple nanofluid flooding method for tertiary or enhanced oil recovery is inefficient, especially when used with low nanoparticle concentration. We have designed and produced a nanofluid of graphene-based amphiphilic nanosheets that is very effective at low concentration. Our nanosheets spontaneously approached the oil-water interface and reduced the interfacial tension in a saline environment (4 wt % NaCl and 1 wt % CaCl 2 ), regardless of the solid surface wettability. A climbing film appeared and grew at moderate hydrodynamic condition to encapsulate the oil phase. With strong hydrodynamic power input, a solid-like interfacial film formed and was able to return to its original form even after being seriously disturbed. The film rapidly separated oil and water phases for slug-like oil displacement. The unique behavior of our nanosheet nanofluid tripled the best performance of conventional nanofluid flooding methods under similar conditions. nanofluid flooding | amphiphilic Janus nanosheets | enhanced oil recovery | climbing film | interfacial film F inding economically viable and environmentally friendly methods to extract the huge amount of residual oil after primary and secondary recovery remains challenging for the oil and gas industry and is also of significant importance in efforts to satisfy the world's increasing energy demand. Nanofluid flooding as an alternative tertiary oil recovery method has been recently reported (1-5). Obviously, simple nanofluid flooding (containing only nanoparticles) at low concentration (0.01 wt % or less) shows the greatest potential from the environmental and economic perspective. Several corresponding oil displacement mechanisms have also been introduced, including reduction of oil-water interfacial tension (6, 7), alteration of rock surface wettability (8-10), and generation of structural disjoining pressure (11-13). However, the oil recovery factor is below 5% with 0.01% nanoparticle loading in core flooding tests in a saline environment (2 wt % or higher NaCl content). Here we show that an oil recovery factor of 15.2% is achieved by using a simple nanofluid of graphene-based Janus amphiphilic nanosheets. To our knowledge, this is the first report of applying nanofluid of amphiphilic Janus two-dimensional materials in tertiary or enhanced oil recovery. We found that in a saline environment, the nanosheets spontaneously approach the oil-water interface, reducing the interfacial tension. A climbing film emerges and encapsulates the oil phase and may carry it forward. Furthermore, we found that a solid-like film forms with strong hydrodynamic power. The film rapidly separates oil and water for slug-like oil displacement. Even though there are ways to achieve 20% enhanced recovery by complicated alkali/surfactant/polymer flooding (14) or by surfactants with added nanoparticles (5), the necessary concentrations of the chemicals and nanoparticles are much higher than 0.01 wt %. Our results provide a nanofluid flooding method for tertiary oil recovery that is compar...

Chromatographic protein separations, immunoassays, and biosensing all typically involve the adsorption of proteins to surfaces decorated with charged, hydrophobic, or affinity ligands. Despite increasingly widespread use throughout the pharmaceutical industry, mechanistic detail about the interactions of proteins with individual chromatographic adsorbent sites is available only via inference from ensemble measurements such as binding isotherms, calorimetry, and chromatography. In this work, we present the direct superresolution mapping and kinetic characterization of functional sites on ion-exchange ligands based on agarose, a support matrix routinely used in protein chromatography. By quantifying the interactions of single proteins with individual charged ligands, we demonstrate that clusters of charges are necessary to create detectable adsorption sites and that even chemically identical ligands create adsorption sites of varying kinetic properties that depend on steric availability at the interface. Additionally, we relate experimental results to the stochastic theory of chromatography. Simulated elution profiles calculated from the molecular-scale data suggest that, if it were possible to engineer uniform optimal interactions into ion-exchange systems, separation efficiencies could be improved by as much as a factor of five by deliberately exploiting clustered interactions that currently dominate the ion-exchange process only accidentally.ion-exchange chromatography | single-molecule kinetics | bioseparations | optical nanoscopy T he hundred-billion-dollar global pharmaceutical industry relies increasingly on the painstaking purification of therapeutic biomolecules such as proteins and nucleic acids (1). Separation of biologics is often performed using ion-exchange chromatography on stationary phases supporting singly charged ligands (2, 3) and constitutes an expensive, bottlenecking step in production. Improving bioseparations is thus highly desirable (4, 5); yet, a molecular-scale, mechanistic understanding is lacking, for ionexchange chromatography in particular (6). Mechanistic detail is lost in ensemble analyses, reflecting the inherent heterogeneity of both the adsorbed biomolecules and the porous stationary phase supports (7). Ensemble adsorption isotherms, however, suggest the likelihood that protein and nucleic acid separations in ion-exchange columns may involve random ligand clustering (8-10). Additional support for such an assertion lies in the implementation of stationary phases of very high charge density by polymerization of charged monomers or layer-by-layer deposition (11-13), and in the demonstration that patches of high charge density on proteins often play a disproportionate role in their adsorption (4,6,(14)(15)(16)(17). In this work, we provide direct evidence of the importance of charge clustering in ion-exchange systems by direct observation of individual adsorption sites.Although the role of multivalency is broadly accepted and exploited in a wide range of associative and adsorption ...