Lifshitz-van Der Waals Forces Research Articles

(Invited) Application of Nanostructure for Improving the Interfacial Interactions between Sensing Surface and Targeted Particles

Various interfacial interactions, encompassing screened Coulomb (electrostatic double layer) forces, Lifshitz-van der Waals forces, hydrophobic/hydrophilic interactions, as well as steric, chemical, morphological, and roughness effects, have been confirmed to play a crucial role in governing the interaction between target particles and the sensing surface. Small protrusions on the sensing surface can induce substantial variations in the surface’s interaction with the target analytes based on the extended Derjauin-Landau-Verwey-Overbeek (DLVO) theory. 1 Here, indium tin oxide coated vertical nanowires served as nanostructure to investigate interfacial interactions between the sensing surface and targeted analytes. Analyzing the ratio of particle size to asperity size on the sensing surface within the extended DLVO theory revealed that surface roughness can provide sufficient interfacial interactions with target analytes, thereby enhancing the electrical sensing performance. Upon immersing the nanostructural sensing surface in an analyte solution, electrical signals undergo a significant shift owing to alterations in the surface potential at the interface between the functionalized sensing surface (such as antibodies or chemical functional groups) and the analyte solution. 2, 3 These observations highlight the critical role of nanostructure on the sensing surface, particularly with adequate surface roughness, in significantly improving sensing performance by facilitating effective interaction of the surface with the target analyte based on the extended DLVO theory.

Efficient, quick, and low-carbon removal mechanism of microplastics based on integrated gel coagulation-spontaneous flotation process

To address the problems of unstable efficiency, long treatment period, and high energy consumption during microplastics (MPs) removal by traditional coagulation–flotation technology, a gel coagulation–spontaneous flotation (GCSF) process is proposed that employs laminarin (LA) as the crosslinker and polyaluminum chloride (PAC)/polyaluminum ferric chloride (PAFC) as the coagulant to remove MPs. Herein, the effects of GCSF chemical conditions on microplastic-humic acid composite pollutants (MP-HAs) removal were investigated, and the removal mechanisms were analyzed through theoretical calculations and floc structure characterization. Results showed that an LA to PAC/PAFC ratio of 2.5:1 achieved the highest removal of HA (86 %) and MPs (93 %–99 %) in short coagulation (< 1 min) and spontaneous flotation (< 9 min) period. PAC-LA exhibited strong removal ability for MP-HAs while PAFC-LA induced fast flotation speed. The peak intensity and peak shift in Fourier-transformed infrared and X-ray photo-electron spectra indicated that the removal mechanisms of MPs include hydrogen bond adsorption and the sweeping effect, mainly relying on –OH/–C = O on the MPs surface and entrapment of gel flocs with a high degree of aggregation, respectively. The extended Derjaguin-Landau-Verwey-Overbeek calculation also revealed that interactions between PAC/PAFC-LA and MP-HAs were mainly polar interaction (hydrogen bonding) and intermolecular attraction interaction (Lifshitz-van der Waals force), and the sweep effect was reflected by intermolecular interaction. In addition, density function theory calculations indicated that –OH in LA mainly adsorbs DO through a double hydrogen bond configuration, and the crosslinking ligand FeO6/AlO6 assists in DO absorption by –OH.

Gravity-driven membrane coupled with oxidation technology to modify the surface properties and biofilm formation: Biofouling mitigation

Biofilms caused by biological fouling play an essential role in gravity-driven membranes’ (GDMs) flux decline and rejection rate. The effects of ozone, permanganate, and ferrate (VI) in-situ pretreatment on membrane properties and biofilm formation were systematically studied. Due to the selective retention and adsorption of algal organic matter by biofilms and oxidative degradation, the rejection efficiency of dissolved organic carbon (DOC) in algae-laden water pretreated with permanganate by GDM was up to 23.63%. Pre-oxidation extraordinarily postponed flux decline and biofilm formation of GDM and reduced membrane fouling. The total membrane resistance decreased by 87.22%–90.30% within 72 h after pre-ozonation. Permanganate was more effective than ozone and ferrate (VI) in alleviating secondary membrane fouling caused by algal cells destroyed by pre-oxidation. Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory revealed that the distribution of electrostatic force (EL), acid-base (AB), and Lifshitz-van der Waals forces (LW) interactions between M. aeruginosa and the released intracellular algogenic organic matter (IOM) and ceramic membrane surface was similar. The membrane and foulants are always attracted to each other by LW interaction at different separation distances. The dominant fouling mechanism of GDM combined with pre-oxidation technology shifts from complete pore blocking to cake layer filtration during operation. After pre-oxidation of algae-laden water by ozone, permanganate, and ferrate (VI), GDM can treat at least 131.8%, 37.0%, and 61.5% more feed solution before forming a complete cake layer. This study provides new insights into the biological fouling control strategies and mechanisms for GDM coupled with oxidation technology, which is expected to alleviate membrane fouling and optimize the feed liquid pretreatment procedure.

Fabrication of polydimethylsiloxane-attached solid slippery surface with high underwater transparency towards the antifouling of optical window for marine instruments

Marine optical instruments are commonly suffering serious biofouling problem caused by the adhesion of marine microorganisms, which severely affects the instruments to monitor the marine environment. Herein, we developed a robust solid slippery surface (SSS) by fabricated a covalently attached polydimethylsiloxane (PDMS) layer on glass substrate to solve the biofouling problem of marine optical instrument windows. The SSS could effectively inhibit the settlements of marine microorganism (bacteria and alga) in various environmental conditions, resulting from the high flexibility of PDMS molecular chains, and thus could maintain its high underwater-transparency. The antifouling mechanism of SSS was results from the weak nonspecific electrostatic Lifshitz-van der Waals forces and less specific hydrogen bonds between SSS and microorganism, which was been confirmed via both single bacterial force spectroscopy measurement and molecular dynamics simulation. Compared with the traditional slippery lubricant-infused porous surface (SLIPS), the SSS exhibited a better robust mechanical stability than that of the SLIPS. In addition, our study provides a valuable method to fabricated the SSS with reliable underwater-transmittance and antifouling properties, which is promised for the applications for the antifouling of marine optical instruments.

Extracellular polymeric substances induced cell-surface interactions facilitate bacteria transport in saturated porous media

Bacteria often respond to dynamic soil environment through the secretion of extracellular polymeric substances (EPS). The EPS modifies cell surface properties and soil pore-scale hydration status, which in turn, influences bacteria transport in soil. However, the effect of soil particle size and EPS-mediated surface properties on bacterial transport in the soil is not well understood. In this study, the simultaneous impacts of EPS and collector size on Escherichia coli (E. coli) transport and deposition in a sand column were investigated. E. coli transport experiments were carried out under steady-state flow in saturated columns packed with quartz sand with different size ranges, including 0.300–0.425 mm (sand-I), 0.212–0.300 mm (sand-II), 0.106–0.150 mm (sand-III) and 0.075–0.106 mm (sand-IV). Bacterial retention increased with decreasing sand collector size, suggesting that straining played an important role in fine-textured media. Both experiment and simulation results showed a clear drop in the retention rate of the bacterial population with the presence of additional EPS (200 mg L−1) (EPS+). The inhibited retention of cells in sand columns under EPS+ scenario was likely attributed to enhanced bacteria hydrophilicity and electrostatic repulsion between cells and sand particles as well as reduced straining. Calculations of the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) interactions energies revealed that high repulsive energy barrier existed between bacterial cells and sand particles in EPS+ environment, primarily due to high repulsive electrostatic force and Lewis acid-base force, as well as low attractive Lifshitz-van der Waals force, which retarded bacterial population deposition. Steric stabilization of EPS would also prevent the approaching of cells close to the quartz surface and thereby hinder cell attachment. This study was the first to show that EPS reduced bacterial straining in saturated porous media. These findings provide new insight into the functional effects of extrinsic EPS on bacterial transport behavior in the saturated soil environment, e.g., aquifers.

Analysis of Molecular Interactions between Components in Phospholipid-Immunosuppressant-Antioxidant Mixed Langmuir Films.

The study of Langmuir monolayers incorporating biomimetic and bioactive substances plays an important role today in assessing the properties and quality of the molecular films for potential biomedical applications. Here, miscibility of binary and ternary monolayers of phospholipid (dioleoyl phosphatidylcholine, DOPC), immunosuppressant (cyclosporine A, CsA), and antioxidant (lauryl gallate, LG) of varying molar fractions was analyzed by means of the Langmuir technique coupled with a surface potential (ΔV) module at the air–water interface. The surface pressure–area per molecule (π–A) isotherms provided information on the physical state of the films at a given surface pressure, the monolayer packing and ordering, and the type and strength of intermolecular interactions. Surface potential–area (ΔV–A) isotherms revealed the molecular orientation changes at the interface upon compression. In addition, the apparent dipole moment of the monolayer-forming molecules was determined from the surface potential isotherms. The obtained results indicated that the film compression provoked subsequent changes of CsA conformation and/or orientation, conferring better affinity for the hydrocarbon environment. The mutual interactions between the components were analyzed here in terms of the excess and total Gibbs energy of mixing, whose values depended on the stoichiometry of the mixed films. The strongest attraction, thus the highest thermodynamic stability, was found for a DOPC–CsA–LG mixture with a 1:1:2 molar ratio. Based on these results, a molecular model for the organization of the molecules within the Langmuir film was proposed. Through this model, we elucidated the significant role of LG in improving the miscibility of CsA in the model DOPC membrane and thus in increasing the stability of self-assembled monolayers by noncovalent interactions, such as H-bonds and Lifshitz–van der Waals forces. The above 1:1:2 combination of three components is revealed as the most promising film composition for the modification of implant device surfaces to improve their biocompatibility. Further insight into mechanisms concerning drug–membrane interactions at the molecular level is provided, which results in great importance for biocoating design and development as well as for drug release at target sites.

A novel optical biosensor for in situ and small-scale monitoring of bacterial transport in saturated columns

In situ monitoring techniques can provide new insight into bacterial transport after inoculating exogenous bacteria into contaminated soils for bioremediation. A real-time and non-destructive optical sensor (the optrode) was employed to monitor in situ transport of two fluorescently labelled bacteria – Green Fluorescent Protein (Gfp)-labelled, hydrophilic Pseudomonas putida and Tomato Fluorescent Protein (td)-labelled, hydrophobic Rhodococcus erythropolis, in a saturated sand column with and without rhamnolipid surfactant. In situ measurements were made at three sampling ports in the column with the optrode in two sets of column experiments. In Experiment 1, liquid samples were extracted for ex situ analyses (plate counts and fluorescence), while in Experiment 2 no liquid samples were extracted. Extracting liquid samples for ex situ analyses in Experiment 1 disturbed in situ measurements; in situ measured bacterial concentrations were lower, or a significant lag in breakthrough occurred relative to ex situ measurements. In Experiment 2, the optrode worked well in monitoring bacterial transport, which gave consistent transport parameters at each sampling port. Moreover, the optrode enabled the impact of bacterial hydrophobicity and rhamnolipid surfactant on bacterial transport to be observed. Specifically, hydrophilic P. putida was transported faster through the column than hydrophobic R. erythropolis; we infer from this result that fewer P. putida cells adsorb to sand particles than do R. erythropolis cells. The rhamnolipid surfactant enhanced the transport of both hydrophilic and hydrophobic bacteria. These two observations are consistent with Lifshitz–van der Waals forces and acid-base interactions between bacteria and sand.

Surface free energy and adhesion energy evaluation of modified bitumen with recycled carbon black (micro-nano) from gases and petrochemical waste

The use of carbon black (CB) obtained from recycling petrochemical waste in bitumen has been reported. In this research, petrochemical waste was recycled and micro-nano CB was produced. Bitumen known as PG64-22 was modified with 3, 5, 7 and 10 wt% of CB and 1, 3, 5 and 7 wt% of nano CB (NCB). NCB particles were evaluated using the scanning electron microscopy and dynamic light scattering test. Stiffness modulus changes of modified bitumen were investigated using the Radovskiy and Teltayev model. Contact angles of three probe liquids, namely water, formamide, and glycerol, were measured on the surface of modified bitumen. The surface free energy parameters like Lifshitz-van der Waals force, polar component and the work of cohesion and adhesion were defined. The results showed that CB and NCB particles increased the penetration index and stiffness modulus of modified bitumen. The total SFE increased more than 50% with 10% CB particles and more than 80% with 7% NCB particles. In addition, the compatibility ratio of limestone and quartzite was revealed to be more than that of granite and sandstone. The results also demonstrated that the wettability of bitumen modified with NCB particles were higher than those modified with CB particles and showed more compatibility ratio values. Moreover, four energy ratios variations of modified bitumen with CB and NCB particles indicated moisture damage performance improvement in the bitumen and aggregate mixes. Also, the results of the indirect tensile strength (ITS) test showed that CB particles in the bitumen led to less reduction of adhesion between bitumen and aggregate compared to the control mixture, leading to an increase in the resistance to moisture damage of asphalt mixture.

Surface-engineered sponges for recovery of crude oil microdroplets from wastewater

In the United States, the oil industry produces over 15 billion barrels of wastewater contaminated with crude oil microdroplets annually. Current methods are ineffective for the removal of these microdroplets at the variable pH conditions commonly found in wastewater. Here, an innovative surface-engineered sponge (SEnS) that synergistically combines surface chemistry, charge and roughness, provides a solution to this problem. Over broad pH conditions, the SEnS rapidly adsorbed oil microdroplets with 95–99% removal efficiency, predominantly facilitated by Lifshitz–van der Waals forces. At the optimum pH, 92% of the oil was adsorbed within 10 min. The oil was subsequently recovered by solvent extraction under ambient conditions, and the cleaned SEnS was reused for oil microdroplets adsorption ten times. The combined efficacy and reusability can enable large-scale removal and recovery of crude oil microdroplets from wastewater. Current methods to remove oil microdroplets from wastewater are ineffective at the variable pH conditions commonly found in wastewater. This study presents a surface-engineered sponge that synergistically combines surface chemistry, charge and roughness, providing a solution to this problem.

A new liquid transport model considering complex influencing factors for nano- to micro-sized circular tubes and porous media

A new liquid transport model in wetted nano- to microsized circular tubes is proposed using basic dynamical analyses that comprehensively consider the Lifshitz–van der Waals force (LWF), the electroviscous force, the weak liquid compressibility, and the Bingham-plastic behavior. The model predicts that the average velocity is initially zero and increases nonlinearly with a concave shape before increasing linearly with the pressure gradient (ΔP/L) and is validated using the experimental data. The threshold pressure gradient (TPG) and the lower limit of the movable-fluid radius (Rm) are calculated based on the proposed model, which are mainly determined by the yield stresses from the Bingham plastic behavior and are also affected by the compressibility and LWF. Considering the microstructural complexity of real porous media, the average velocity model is also applicable for tight porous media with a capillary equivalent radius from the permeability. The calculated average velocity is non-Darcy with TPG. The TPG decreases as the permeability increases, and the Rm decreases with the pressure gradient in the low range and remains constant at the higher ranges, which is primarily between 10 and 30 nm. All these results for porous media are compared with the experimental data of core seepage and show good agreement in general. The proposed model has a clear parametric representation compared with previous nonlinear models. It explains the underlying reasons for the nonlinear, low-velocity flow mechanism in nano- to microsized tubes and pores and provides theoretical guidance for liquid transport in porous media and oil recovery from tight oil reservoirs.

Size-Dependent Bacterial Toxicity of Hematite Particles.

Submicron-sized iron oxide particles can influence the activity of bacteria, but the exact mechanisms of oxide toxicity toward bacteria remain elusive. By using atomic force microscopy (AFM), soft X-ray tomography (Nano-CT), and Fourier transform infrared (FTIR) spectrometry, we show how the size-dependent interfacial interactions between hematite particles and bacteria in the absence of any ligands contribute to the antimicrobial properties against Gram-positive and Gram-negative bacterial strains. We found that surface adhesion between hematite particles and bacterial cells is initially dominated by Lifshitz van der Waals and electrostatic forces. Subsequently, the rapid formation of P-O-Fe bonds occurs, followed by changes in the structures of membrane proteins in 2 h, resulting in the loss of the structural integrity of the membrane within 10 h. Thus, particles can migrate into the cells. After contact with bacterial cells, reactive oxygen species are generated on the surface of hematite particles, leading to cell permeabilization. G- bacteria appear to be more susceptible to this process than G+ bacteria because the latter exhibit weaker adhesion forces toward hematite and benefit from the protective effects of the peptidoglycan layers. Our work revealed that hematite nanoparticles are more toxic to bacteria than microscaled particles due to their strong interfacial physicochemical interactions with the cells.

Synthesis, aggregation behavior of polyether based carbosilane surfactants in aqueous solution

Novel polyether based carbosilane surfactants with different hydrophobic groups (Me-Si2C-EO8, Et-Si2C-EO8, and Ph-Si2C-EO8) were successfully synthesized and confirmed by 1H NMR, 13C NMR, 29Si NMR, and FT-IR. Aggregation behavior of the polyether based carbosilane surfactants in aqueous solution was investigated by surface tension, dynamic light scattering (DLS), transmission electron microscopy (TEM). The additional CH2 group between silicon atoms can increase the Lifshitz-van der Waals forces for carbosilane hydrophobic groups and directly increases the γcmc and Amin values. The γcmc and Amin values follow the order, Me-Si2C-EO8 < Et-Si2C-EO8 < Ph-Si2C-EO8, owing to the introduction of ethyl, phenyl group to carbosilane hydrophobic groups which can obviously increase their molecular volumes and hydrophobicities. All the investigated carbosilane surfactants can self-assemble into spherical aggregates with size distribution ranges from 50 to 400 nm in aqueous solution.

Acid-Base Polymeric Foams for the Adsorption of Micro-oil Droplets from Industrial Effluents.

Separation of toxic organic pollutants from industrial effluents is a great environmental challenge. Herein, an acid-base engineered foam is employed for separation of micro-oil droplets from an aqueous solution. In acidic or basic environments, acid-base polymers acquire surface charge due to protonation or dissociation of surface active functional groups. This property is invoked to adsorb crude oil microdroplets from water using polyester polyurethane (PESPU) foam. The physicochemical surface properties of the foam were characterized using X-ray photoelectron spectroscopy, inverse gas chromatography, electrokinetic analysis, and micro-computed tomography. Using the surface charge of the foam and oil droplets, the solution pH (5.6) for maximum separation efficacy was predicted. This optimal pH was verified through underwater wetting behavior and adsorption experiments. The droplet adsorption onto the foam was governed by physisorption, and the driving forces were attributed to electrostatic attraction and Lifshitz-van der Waals forces. The foam was regenerated and reused multiple times by simple compression. The lowest trace oil content in the retentate was 3.6 mg L-1, and all oil droplets larger than 140 nm were removed. This work lays the foundation for the development of a new class of engineered foam adsorbents with the potential to revolutionize water treatment technologies.

The Effects of Noncellulosic Compounds on the Nanoscale Interaction Forces Measured between Carbohydrate-Binding Module and Lignocellulosic Biomass.

The lack of fundamental understanding of the types of forces that govern how cellulose-degrading enzymes interact with cellulosic and noncellulosic components of lignocellulosic surfaces limits the design of new strategies for efficient conversion of biomass to bioethanol. In a step to improve our fundamental understanding of such interactions, nanoscale forces acting between a model cellulase-a carbohydrate-binding module (CBM) of cellobiohydrolase I (CBH I)-and a set of lignocellulosic substrates with controlled composition were measured using atomic force microscopy (AFM). The three model substrates investigated were kraft (KP), sulfite (SP), and organosolv (OPP) pulped substrates. These substrates varied in their surface lignin coverage, lignin type, and xylan and acetone extractives' content. Our results indicated that the overall adhesion forces of biomass to CBM increased linearly with surface lignin coverage with kraft lignin showing the highest forces among lignin types investigated. When the overall adhesion forces were decoupled into specific and nonspecific component forces via the Poisson statistical model, hydrophobic and Lifshitz-van der Waals (LW) forces dominated the binding forces of CBM to kraft lignin, whereas permanent dipole-dipole interactions and electrostatic forces facilitated the interactions of lignosulfonates to CBM. Xylan and acetone extractives' content increased the attractive forces between CBM and lignin-free substrates, most likely through hydrogen bonding forces. When the substrates treated differently were compared, it was found that both the differences in specific and nonspecific forces between lignin-containing and lignin-free substrates were the least for OPP. Therefore, cellulase enzymes represented by CBM would weakly bind to organosolv lignin. This will facilitate an easy enzyme recovery compared to other substrates treated with kraft or sulfite pulping. Our results also suggest that altering the surface hydrophobicity and the surface energy of lignin that facilitates the LW forces should be a priori to avoid nonproductive binding of cellulase to kraft lignin.

Quantum vacuum photon modes and repulsive Lifshitz–van der Waals interactions

The bridge between quantum vacuum photon modes and properties of patterned surfaces is currently being established on solid theoretical grounds. Based on these foundations, the manipulation of quantum vacuum photon modes in a nanostructured cavity is theoretically shown to be able to turn the Lifshitz-van der Waals forces from attractive to repulsive regime. Since this concept relies on surface nanopatterning instead of chemical composition changes, it drastically relaxes the usual conditions for achieving repulsive Lifshitz-van der Waals forces. As a case study, the potential interaction energy between a nanopatterned polyethylene slab and a flat polyethylene slab with water as intervening medium is calculated. Extremely small corrugations heights (less than ten nanometers) are shown to be able to turn the Lifshitz-van der Waals force from attractive to repulsive, the interaction strength being controlled by the corrugation height. This new approach could lead to various applications in surface science.

Characterization of asphaltene deposition in a stainless steel tube

In this study, the mechanism and kinetics of asphaltene deposition in stainless steel tubes have been studied experimentally using n-heptane as the precipitant. The effects of oil velocity, temperature, and oil–precipitant volumetric dilution ratio on the rate of asphaltene deposition are investigated. Since the adhesion of asphaltenes on to the metal surface is controlled by its transport through the laminar sub layer, our focus was limited to studying the phenomena in laminar flow regime. The concentration of asphaltenes was measured using UV–visible spectrophotometer at 650 nm wavelength. This enabled us to accurately measure the amount and extent of asphaltene deposits in the stainless steel tube. It is observed that the deposition process is often accompanied by significant erosion due to the subsequent dominance of shear forces on the asphaltene deposits. However, the erosion is not complete and a certain layer of asphaltene deposits remain before the deposition process becomes dominant. The initial rate of asphaltene deposition increases with the increase in oil velocity and temperature. The deposition rates increase with the decrease in the oil–precipitant volumetric dilution ratio. The asphaltene deposits were also subjected to X-ray photoelectron spectroscopy to characterize the surface composition of atoms responsible for the interfacial interaction forces due to the surface functional groups. The fundamental interaction forces between asphaltenes and a stainless steel surface was measured by using inverse gas chromatography. The surface energy of stainless steel indicated the amphoteric nature of the surface, with a slightly higher basic component. The surface energy of asphaltenes displayed a very high component of Lifshitz–van der Waals forces. However the polar component of surface energy of asphaltenes could not be measured due to its very strong interaction with the polar probes on account of its polarity.

Influence of oxygen‐inhibited layer on dentin bond strength of chemical‐cured resin composite

This study evaluated the influence of an oxygen-inhibited layer on the surface free energies of three single-step self-etch adhesives and on the bond strength of chemical-cured resin. Adhesives were applied to bovine dentin and light irradiated, and the oxygen-inhibited layer was either retained or removed. Surface free energies were determined by measuring the contact angles of test liquids placed on the cured adhesives. Dentin bond strengths of chemical-cured resin with and without the oxygen-inhibited layer were measured. Ultrastructural observation of the restorative-dentin interface was made by scanning electron microscopy. For all surfaces, values of the estimated surface tension component, Lifshitz-Van der Waals force (γS(LW)), were relatively constant. Values for the Lewis acid (γS(+)) component increased slightly when the oxygen-inhibited layer was removed, whereas those of the Lewis base (γS(-)) component decreased significantly. The bond strength of the chemical-cured resin composite was significantly higher in specimens without an oxygen-inhibited layer (7.6-8.0 MPa) than in those with an oxygen-inhibited layer (4.8-5.2 MPa). Small gaps between adhesive and resin composite were found for the group with an oxygen-inhibited layer. These results indicate that the absence of an oxygen-inhibited layer in single-step self-etch adhesives promotes higher dentin bond strength of the chemical-cured resin.

Combined Poisson and Soft-Particle DLVO Analysis of the Specific and Nonspecific Adhesion Forces Measured between L. monocytogenes Grown at Various Temperatures and Silicon Nitride

Adhesion forces between pathogenic L. monocytogenes EGDe and silicon nitride (Si(3)N(4)) were measured using atomic force microscopy (AFM) under water and at room temperature for cells grown at five different temperatures (10, 20, 30, 37, and 40 °C). Adhesion forces were then decoupled into specific (hydrogen bonding) and nonspecific (electrostatic and Lifshitz-van der Waals) force components using Poisson statistical analysis. The strongest specific and nonspecific attraction forces were observed for cells grown at 30 °C, compared to those observed for cells grown at higher or lower temperatures, respectively. By combining the results of Poisson analysis with the results obtained through soft-particle Derjaguin-Landau-Verwey-Overbeek (DLVO) analysis, the contributions of the Lifshitz-van der Waals and electrostatic forces to the overall nonspecific interaction forces were determined. Our results showed that the Lifshitz-van der Waals attraction forces dominated the total nonspecific adhesion forces for all investigated thermal conditions. However, irrespective of the temperature of growth investigated, hydrogen bonding forces were always stronger than the nonspecific forces. Finally, by combining Poisson analysis with soft-particle analysis of DLVO forces, the closest separation distances where the irreversible bacterial adhesion takes place can be determined relatively easily. For all investigated thermal conditions, the closest separation distances were <1 nm.

Drainage and rupture of thin foam films in the presence of ionic and non-ionic surfactants

The thin film pressure balance technique was used to determine the overall magnitude of the surface forces in foam films stabilized by flotation reagents such as sodium dodecyl sulfate and polypropylene glycol at high NaCl concentrations. The Stefan–Reynolds lubrication approximation was used to estimate the forces from measured film thinning rates while the capillary wave model of Valkovska, Danov and Ivanov was used to calculate the forces from measured critical rupture thicknesses. It was found that at very low surfactant concentrations commensurate with typical flotation reagent dosage, the overall forces were attractive and up to one order of magnitude stronger than the Lifshitz–van der Waals forces. The forces became smaller with increasing surfactant concentration. It was also found that the forces obtained from the capillary wave theory were indifferent to changes in film radii and surface mobility, in contrast to the Reynolds lubrication approximation. For comparison, other film drainage models considering film surface mobility and hydrodynamic corrugation were used to fit the present experimental thinning curves obtained at very low surfactant concentrations. They also showed that the overall attraction forces were several times stronger than the Lifshitz–van der Waals forces.

Statistical Analysis of Long- and Short-Range Forces Involved in Bacterial Adhesion to Substratum Surfaces as Measured Using Atomic Force Microscopy

Surface thermodynamic analyses of microbial adhesion using measured contact angles on solid substrata and microbial cell surfaces are widely employed to determine the nature of the adhesion forces, i.e., the interplay between Lifshitz-van der Waals and acid-base forces. While surface thermodynamic analyses are often viewed critically, atomic force microscopy (AFM) can also provide information on the nature of the adhesion forces by means of Poisson analysis of the measured forces. This review first presents a description of Poisson analysis and its underlying assumptions. The data available from the literature for different combinations of bacterial strains and substrata are then summarized, leading to the conclusion that bacterial adhesion to surfaces is generally dominated by short-range, attractive acid-base interactions, in combination with long-range, weaker Lifshitz-van der Waals forces. This is in line with the findings of surface thermodynamic analyses of bacterial adhesion. Comparison with single-molecule ligand-receptor forces from the literature suggests that the short-range-force contribution from Poisson analysis involves a discrete adhesive bacterial cell surface site rather than a single molecular force. The adhesion force arising from these cell surface sites and the number of sites available may differ from strain to strain. Force spectroscopy, however, involves the tedious task of identifying the minor peaks in the AFM retraction force-distance curve. This step can be avoided by carrying out Poisson analysis on the work of adhesion, which can also be derived from retraction force-distance curves. This newly proposed way of performing Poisson analysis confirms that multiple molecular bonds, rather than a single molecular bond, contribute to a discrete adhesive bacterial cell surface site.