Derjaguin-Landau-Verwey-Overbeek Predictions Research Articles

Effect of Clay Colloid Particles on Formaldehyde Transport in Unsaturated Porous Media

This study examines the effects of two representative colloid-sized clay particles (kaolinite, KGa-1b and montmorillonite, STx-1b) on the transport of formaldehyde (FA) in unsaturated porous media. The transport of FA was examined with and without the presence of clay particles under various flow rates and various levels of saturation in columns packed with quartz sand, under unsaturated conditions. The experimental results clearly suggested that the presence of clay particles retarded by up to ~23% the transport of FA in unsaturated packed columns. Derjaguin–Landau–Verwey–Overbeek (DLVO) interaction energy calculations demonstrated that permanent retention of clay colloids at air-water interfaces (AWI) and solid-water interfaces (SWI) was negligible, except for the pair (STx-1b)–SWI. The experimental results of this study showed that significant clay colloid retention occurred in the unsaturated column, especially at low flow rates. This deviation from DLVO predictions may be explained by the existence of additional non-DLVO forces (hydrophobic and capillary forces) that could be much stronger than van der Waals and double layer forces. The present study shows the important role of colloids, which may act as carriers of contaminants.

Adhesion mediated transport of bacterial pathogens in saturated sands coated by phyllosilicates and Al-oxides

The current knowledge of bacterial migration is mainly derived from work using bare or Fe-coated quartz sands as porous media. However, mineral coatings on quartz by phyllosilicates and Al-oxides prevail in natural soils, and their effect on bacterial transport remains unknown. Herein, we systematically explored the transport of two bacterial pathogens (Escherichia coli and Staphylococcus aureus) through saturated bare quartz and those coated by kaolinite (KaoQuartz), montmorillonite (MontQuartz) or Al-oxides (AlQuartz) under various solution ionic strength (IS) and pH levels. Elevating IS or decreasing pH discouraged bacterial mobility in all cases, with one exception for the migration of S. aureus through AlQuartz at various IS levels. E. coli showed a higher mobility than S. aureus in all cases. All the three coatings, especially the Al-oxides inhibited bacterial transport through quartz. Overall, the two phyllosilicates-coated sands showed transport behaviors (mobility trends with IS, pH, and cell type) similar to those for the bare quartz which could be explained by the Derjaguin–Landau–Verwey–Overbeek (DLVO) theory. Nevertheless, for transport within AlQuartz, there were deviations between the observations and the DLVO predictions, probably because of the existence of non-DLVO forces such as hydrophobic and chemical interactions. More importantly, the bacterial retention was found to correlate well with the adhesion regardless of the solution condition and the bacteria and media type, thereby revealing a central role of adhesion in mediating migration through mineral-coated sands. These findings highlight the significance of mineral coating and adhesion in pathogen dissemination in natural soils.

Non-additivity of pair interactions in charged colloids.

It is general wisdom that the pair potential of charged colloids in a liquid may be closely approximated by a Yukawa interaction, as predicted by the classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. We experimentally determine the effective forces in a binary mixture of like-charged particles, of species 1 and 2, with blinking optical tweezers. The measured forces are consistent with a Yukawa pair potential but the (12) cross-interaction is not equal to the geometric mean of the (11) and (22) like-interactions, as expected from DLVO. The deviation is a function of the electrostatic screening length and the size ratio, with the cross-interaction measured being consistently weaker than DLVO predictions. The corresponding non-additivity parameter is negative and grows in magnitude with increased size asymmetry.

The role of electrostatic interactions in adhesion of Streptococcus thermophilus to human erythrocytes in media with different 1:1 and 2:1 electrolyte concentrations

The process of bacterial adhesion is usually discussed in terms of a two-stage sorption model. According to this model, at the first stage bacteria rapidly attach to the surface by weak physical interactions, while at the second stage irreversible molecular and cellular adhesion processes take place. An important factor, influencing the adhesion processes, is physical and chemical characteristics of the medium, in particular, the presence of monovalent and bivalent cations. In this work, we assessed the role of electrostatic component of the intercellular interactions in the media with different electrolyte concentrations (namely, 1:1 and 2:1) at the first reversible stage of adhesion and probability of further specific binding. We compared experimental data of lactobacilli Streptococcus thermophilus adhesion to human erythrocytes with theoretical Debye radius and surface potential of erythrocytes in the experimental solutions of 1:1 electrolyte. Our results showed that with decreasing ionic strength of the solution, the change in the adhesion index in our experiments is fully in line with the theory DLVO (Derjaguin–Landau–Verwey–Overbeek) predictions. The experimental results were obtained and theoretical calculations of the electrostatic interactions parameters in the experimental solutions of 2:1 electrolyte once again confirmed the acceptability of a two-stage model of sorption and DLVO theory to describe a cell–cell adhesion.

Aggregation kinetics of CeO2 nanoparticles in KCl and CaCl2 solutions: measurements and modeling

To characterize the environmental transport and health risks of CeO2 nanoparticles (NPs), it is important to understand their aggregation behavior. This study investigates the aggregation kinetics of CeO2 NPs in KCl and CaCl2 solutions using time-resolved dynamic light scattering (TR-DLS). The initial hydrodynamic radius of CeO2 NPs measured by DLS was approximately 95 nm. Attachment efficiencies were derived both from aggregation data and predictions based on the Derjaguin–Landau–Verwey–Overbeek (DLVO) theory. The deviations of the DLVO predictions were corrected by employing the extended DLVO (EDLVO) theory. The critical coagulation concentration (CCC) of CeO2 NPs at pH = 5.6 is approximately 34 mM for KCl and 9.5 mM for CaCl2. Furthermore, based on the EDLVO theory and the von Smoluchowski’s population balance equation, a model accounting for diffusion-limited aggregation (DLA) kinetics was established. For the reaction-limited aggregation (RLA) kinetics, a model that takes fractal geometry into account was established. The models fitted the experimental data well and proved to be useful for predicting the aggregation kinetics of CeO2 NPs.

Analysis of Force Interactions between AFM Tips and Hydrophobic Bacteria Using DLVO Theory

Microbial adhesion to surfaces and interfaces is strongly influenced by their structure and physicochemical properties. We used atomic force microscopy (AFM) to measure the forces between chemically functionalized AFM tips and two bacterial species exhibiting different cell surface hydrophobicities, measured as the oil/water contact angle (theta): Acinetobacter venetianus RAG-1 (theta = 56.4 degrees ) and Rhodococcus erythropolis 20S-E1-c (theta = 152.9 degrees ). The forces were measured as the AFM tips, coated with either hydrophobic (octadecane) or hydrophilic (undecanol) groups, approached the bacterial cells in aqueous buffer. The experimental force curves between the two microbial cells and functionalized AFM probes were not successfully described by the classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory of colloid stability. To reconcile the discrepancy between theory and experiments, two types of extended DLVO models were proposed. The first modification considers an additional acid-base component that accounts for attractive hydrophobic interactions and repulsive hydration effects. The second model considers an additional exponentially decaying steric interaction between polymeric brushes in addition to the acid-base interactions. These extended DLVO predictions agreed well with AFM experimental data for both A. venetianus RAG-1, whose surface consists of an exopolymeric capsule and pili, and R. erythropolis 20S-E1-c, whose surface is covered by an exopolymeric capsule. The extended models for the bacteria-AFM tip force-distance curves were consistent with the effects of steric interactions.

The initial single yeast cell adhesion on glass via optical trapping and Derjaguin–Landau–Verwey–Overbeek predictions

We used an optical tweezer to investigate the adhesion of yeast Saccharomyces cerevisiae onto a glass substrate at the initial contact. Micromanipulation of free-living objects with single-beam gradient optical trap enabled to highlight mechanisms involved in this initial contact. As a function of the ionic strength and with a displacement parallel to the glass surface, the yeast adheres following different successive ways: (i) Slipping and rolling at 1.5 mM NaCl, (ii) slipping, rolling, and sticking at 15 mM NaCl, and (iii) only sticking at 150 mM. These observations were numerous and reproducible. A kinetic evolution of these adhesion phenomena during yeast movement was clearly established. The nature, range, and relative intensity of forces involved in these different adhesion mechanisms have been worked out as a quantitative analysis from Derjaguin-Landau-Verwey-Overbeek (DLVO) and extended DLVO theories. Calculations show that the adhesion mechanisms observed and their affinity with ionic strength were mainly governed by the Lifshitz-van der Waals interaction forces and the electrical double-layer repulsion to which are added specific contact forces linked to "sticky" glycoprotein secretion, considered to be the main forces capable of overcoming the short-range Lewis acid-base repulsions.

Role of Solution Chemistry and Ion Valence on the Adhesion Kinetics of Groundwater and Marine Bacteria

The role of solution chemistry on bacterial adhesion has been investigated using a radial stagnation point flow (RSPF) system. This experimental system utilized an optical microscope and an image-capturing device to directly observe the deposition kinetics of a groundwater bacterium, Burkholderia cepacia G4g, and a marine bacterium, Halomonas pacifica g. Experiments were carried out under well-controlled hydrodynamic and solution chemistry conditions, allowing for the sensitivity of bacterial adhesion behavior to be examined under a range of ionic strength and valence (KCl vs CaCl2) simulating groundwater and marine environments. Complimentary cell characterization techniques were conducted to evaluate the electrophoretic mobility, hydrophobicity, surface charge density, and viability of the bacteria under the same range of conditions. Solution chemistry was found to have a marked effect on the electrokinetic and surface properties of bacteria and the quartz collector, as well as on the resulting rate of bacterial deposition. Comparable adhesion trends were observed for B. cepacia G4g and H. pacifica g. Specifically, the deposition rates of the two bacteria species in both KCl and CaCl2 solutions increased with ionic strength, a trend consistent with traditional Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, which considers the combination of van der Waals and electrostatic double-layer interaction forces. However, in some cases, experimental results showed bacterial deposition behavior to deviate from DLVO predictions. On the basis of the systematic investigation of bacterial cell characteristics, it was found that Ca2+ ions play a distinct role on bacterial surface charge, hydrophobicity, and deposition behaviors. It is further suggested that bacterial adhesion is determined by the combined influence of DLVO interactions, electrosteric interactions associated with solution chemistry, and the hydrodynamics of the deposition system.

Experimentally Derived Sticking Efficiencies of Microparticles Using Atomic Force Microscopy

The sticking efficiencies (alpha) of colloidal particles have been derived from the intersurface potential energy between 2 microm carboxylated polystyrene microspheres and a silica glass plate using the interaction force boundary layer model. The intersurface potential energies were calculated from force-distance data measured using atomic force microscopy (AFM) and from calculations based on Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. AFM forces were measured in aqueous solutions over a range of pH and ionic strength conditions, and DLVO calculations were performed on identical systems. In most conditions, sticking efficiencies that were calculated from AFM data are considerably largerthan values calculated from DLVO predictions. Sticking efficiencies vary between 0 and 1 and are strongly dependent upon solution chemistry. AFM-derived sticking efficiencies are consistent with measured microsphere and collector zeta-potentials; sticking efficiencies are lower for more negatively charged surfaces. These results provide the first alpha estimates of a microparticle-collector system that are calculated directly from physically measured interfacial nanoforces. This study clearly demonstrates that significant differences exist between DLVO- and AFM-derived sticking efficiencies.

Directed Assembly and Rupture Mechanics of Colloidal Aggregates

The macroscopic rheological behavior of colloidal gels arises from the micromechanical properties of the gel backbone, which are governed by nanoscale particle interactions. These colloidal interactions have been commonly understood in terms of the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. Recent work has shown, however, that nonidealities, such as surface roughness and charge nonuniformity, may cause the particle interactions to significantly deviate from DLVO predictions at near-contact separations. Here we present novel techniques for directing the assembly of colloidal aggregates that mimic the gel backbone, based on optical micromanipulation of multiple particles using laser tweezers. This also provides an in situ method for measuring near-contact interactions via single-bond rupture forces. We find that PMMA particles aggregated in the presence of nonorganic salts exhibit interparticle bond strengths more than 10 times greater than those predicted by DLVO theory. However, good agreement is found with DLVO predictions when the anionic surfactant sodium dodecyl sulfate (SDS) is used as the flocculant.

Double Layer Forces over Large Potential Ranges as Measured in an Electrochemical Surface Forces Apparatus

Electrodes specifically designed for use in the surface forces apparatus (SFA) were employed to study forces between mica and polycrystalline gold under potential control. This control was achieved by soldering a wire to the gold surface and modifying the chamber of the SFA into a three-electrode cell configuration. The interactions measured were a strong function of the applied electrode potential, being more repulsive as the gold potential was moved toward more negative potentials. Independent force measurements between mica surfaces were done to determine the mica surface potential. The experimental results were compared to Derjaguin−Landau−Verwey−Overbeek (DLVO) predictions of the forces between dissimilar charged surfaces. The long range forces correspond well to DLVO predictions, including evidence of saturation in forces at high applied potentials; forces deviate from theory at short range.