Analytical study of pulsatile mixed electroosmotic and shear-driven flow in a microchannel with a slip-dependent zeta potential

The escalation of zeta potential by the influence of wall slip for the electrokinetically modulated flow through a microchannel motivates to consider the impact of hydrodynamic slippage upon the zeta or surface potential.The reported study undergoes an analytical exploration of the pulsatile electroosmosis and shear-actuated flow characteristics of a fluid with a Newtonian model through a microchannel with parallel plates by invoking the reliance of a zeta or surface potential on slippage.The linearized Poisson-Boltzmann and momentum equations are solved analytically to obtain the explicit expression of the electrical potential induced in the electrical double layer(EDL),the flow velocity field,and the volumetric flow rate for an extensive span of parameters.The velocity field proximal to the microchannel wall is observed to enhance by an apparent zeta potential,and is further escalated for a thinner EDL and an oscillating electric field with a higher amplitude.However,near the core region of the microchannel,the flow velocity becomes invariant with the EDL thickness.The result shows that the lower wall velocity contributes to the flow velocity along with the electroosmotic body force and the impact of the velocity of the wall underneath diminishes proximal to the upper wall.Moreover,the volumetric flow rate increases when the thickness of the EDL decreases,owing to the influence of the wall slip.However,for thinner EDLs and medium and higher oscillating Reynolds numbers,the volumetric flow rate varies non-monotonously,correlative to the slip-free and slip cases.

Correlation Evaluation of Ion Adsorption-Based Rare Earth Leaching Performance Based on Zeta Potential Drop Leaching

Rare earth elements are indispensable raw materials for advanced aero-engines, special optical materials, and high-performance electronic products. With the development of the social economy, the global demand for rare earth resources is increasing, and rare earths have become a key metal for the development of new industries and frontier technologies that are highly valued both at home and abroad. Ion-adsorbed rare earth ores are an important source of rare earths, so the efficient green leaching of ion-adsorbed rare earths is important. Researchers found that the selection of an efficient green leaching agent for ion-adsorbed rare earths is based on the zeta potential of tailing clay minerals in addition to leaching efficiency, and both zeta potential and leaching ion concentration are related to mineral acidity and alkalinity, and the pH of tailing water suspension is a direct indicator of environmental water quality requirements. Therefore, the efficiency of the leaching process is closely integrated with the environmental evaluation, and the characteristics and correlation of the changes in zeta potential, pH, conductivity and pollutant concentration of the pulp of clay mineral content during the leaching process of ore leaching and tailings aqueous electrolyte solution leaching are studied by evaluating the leaching system, and a set of correlation leaching efficiency and environmental impact evaluation method is established based on the results of the above analysis, which is of scientific development of ion adsorption rare earth resources. It has important theoretical significance and practical application value.

An experimental study on size distribution and zeta potential of bulk cavitation nanobubbles

Nanobubble flotation technology is an important research topic in the field of fine mineral particle separation.The basic characteristics of nanobubbles,including their size,concentration,surface zeta potential,and stability have a significant impact on the nanobubble flotation performance.In this paper,bulk nanobubbles generated based on the principle of hydrodynamic cavitation were investigated to determine the effects of different parameters(e.g.,surfactant(frother)dosage,air flow,air pressure,liquid flow rate,and solution pH value)on their size distribution and zeta potential,as measured using a nanoparticle analyzer.The results demonstrated that the nanobubble size decreased with increasing pH value,surfactant concentration,and cavitation-tube liquid flow rate but increased with increasing air pressure and increasing air flow rate.The magnitude of the negative surface charge of the nanobubbles was positively correlated with the pH value,and a certain relationship was observed between the zeta potential of the nanobubbles and their size.The structural parameters of the cavitation tube also strongly affected the characteristics of the nanobubbles.The results of this study offer certain guidance for optimizing the nanobubble flotation technology.

Preparation of Polycarboxylate-based Superplasticizer and Its Effects on Zeta Potential and Rheological Property of Cement Paste

A series of polycarboxylate-based superplasticizers(PCs) with different structures were synthesized and the effects of chemical structure on zeta potential and rheological property of cement paste were studied. Residual monomers in each sample of PCs were quantitatively determined. The property of the polymers in cement was tested by micro-electrophoresis apparatus and R/S rheometer. Results showed that the zeta potential and its rheological properties are related with the side-chain length and density of PCs. The PCs having shorter side chain and lower side chain density exhibit higher anionic charge density, thus resulting in higher zeta potential. The effect of side chain density on zeta potential is more notable compared with that of side-chain length, and thus affecting the initial shear yield stress and apparent viscosity of the cement paste. In addition, although increasing the side chain length will result in reduction of the anionic charge density, the steric hindrance effect is obvious, which can effectively improve the dispersion of the cement particles, and reduce the viscosity and shear yield stress of slurry.

Ionic Distribution, Electrostatic Potential and Zeta Potential at Electrochemical Interfaces

Density functional theory is applied to predicting the structures and electrostatic potentials of planar electrochemical surfaces within the framework of the restricted primitive model where small ions are represented by charged hard spheres of equal diameter and the solvent is assumed to be a continuous dielectric medium. The hard-sphere contribution to the excess Helmholtz energy functional is evaluated using the modified fundamentalmeasure theory and the electrostatic contribution is obtained from the quadratic functional Taylor expansion using the second-order direct correlation function from the mean-spherical approximation. Numerical results for the ionic density profiles and the mean electrostatic potentials near a planar surface of various charge densities are in excellent agreement with molecular simulations. In contrast to the modified Gouy-Chapman theory, the present density functional theory correctly predicts the second layer formation and charge inversion of charged surfaces as observed in simulations and in experiments. The theory has also been tested with the zeta potentials of positively charged polystyrene particles in aqueous solutions of KBr. Good agreement is achieved between the calculated and experimental results.

Zeta Potential and Rheological Behavior of ULC Castables Matrix

Effects of starting materials and four dispersants （ STP, SHP, FDN and FS60 ） on Zeta potential and rheological behavior of alumina based ULC castables matrix were investigated. The results show that： characteristics of silica fume and alumina cements play a very important role in Zeta potential and viscosity of suspensions of the castables matrix; the dispersants STP and SHP can change Zeta potential values of the matrix suspensions remarkably; the four dispersants can effectively improve the rheological properties of matrix suspensions. For the point of lower viscosity of the matrix suspensions, the suitable additions of the three dispersants （ SHP , FDN and FS60 ） are about 0. 2% while that of STP is about 0. 3%.

Application of ion-engineered Persian Gulf seawater in EOR:effects of different ions on interfacial tension,contact angle,zeta potential,and oil recovery

In this study,we initially performed interfacial tension(IFT)tests to investigate the potential of using the Persian Gulf seawater(PGSW)as smart water with diferent concentrations of NaCl,KCl,MgCl_(2),CaCl_(2),and Na_(2)SO_(4).Next,for each salt,at the concentration where IFT was minimum,we conducted contact angle,zeta potential,and micromodel fooding tests.The results showed that IFT is minimized if NaCl or KCl is removed from PGSW;thus,for solutions lacking NaCl and KCl,the IFT values were obtained at 26.29 and 26.56 mN/m,respectively.Conversely,in the case of divalent ions,minimum IFT occurred when the concentration of MgCl_(2),CaCl_(2),and Na_(2)SO_(4) in PGSW increased.Specifcally,a threefold rise in the concentration of Na_(2)SO_(4) further reduced IFT as compared to optimal concentrations of MgCl_(2) or CaCl_(2).It should be mentioned that eliminating NaCl from PGSW resulted in the lowest IFT value compared to adding or removing other ions.Whereas the removal of NaCl caused the contact angle to decrease from 91.0°to 67.8°relative to PGSW and changed surface wettability to weakly water-wet,eliminating KCl did not considerably change the contact angle,such that it only led to a nine-degree reduction in this angle relative to PGSW and left wettability in the same neutral-wet condition.At optimal concentrations of MgCl_(2),CaCl_(2),and Na_(2)SO_(4),only an increase in Na_(2)SO_(4) concentration in PGSW could change wettability from neutral-wet to weakly water-wet.For solutions with optimal concentrations,the removal of NaCl or KCl caused the rock surface to have slightly higher negative charges,and increasing the concentration of divalent ions led to a small reduction in the negative charge of the surface.The results of micromodel fooding indicated that NaCl-free PGSW could raise oil recovery by 10.12%relative to PGSW.Furthermore,when the Na_(2)SO_(4) concentration in PGSW was tripled,the oil recovery increased by 7.34%compared to PGSW.Accordingly,depending on the conditions,it is possible to use PGSW so as to enhance the efciency of oil recovery by removing NaCl or by increasing the concentration of Na_(2)SO_(4) three times.

Pulsatile electroosmotic flow of a Maxwell fluid in a parallel flat plate microchannel with asymmetric zeta potentials

The pulsatile electroosmotic flow （PEOF） of a Maxwell fluid in a parallel flat plate microchannel with asymmetric wall zeta potentials is theoretically analyzed. By combining the linear Maxwell viscoelastic model, the Cauchy equation, and the electric field solution obtained from the linearized PoissomBoltzmann equation, a hyperbolic par- tial differential equation is obtained to derive the flow field. The PEOF is controlled by the angular Reynolds number, the ratio of the zeta potentials of the microchannel walls, the electrokinetic parameter, and the elasticity number. The main results obtained from this analysis show strong oscillations in the velocity profiles when the values of the elas- ticity number and the angular Reynolds number increase due to the competition among the elastic, viscous, inertial, and electric forces in the flow.

THE DETERMINATION OF ZETA POTENTIAL IN THE COLLOID α-FeOOH/NaCl aq.BY THE APPLICATION OF STIGTER-OHSHIMA THEORIES

The electrophoretic mobility of positively charged,cylindrically shaped α-FeO OH particles dispersed in dilute sodium chloride solutions was measured at 25℃,as a function of ionic strength and pH using microelectrophoresis apparatus. The mobility data were processed through a number of selected relationships that represent various stages of understanding of electrophoretic theory,culminating in the determination of values of the electrokinetic charge and zeta potential of the colloid α-FeO OH/NaCl aq.

The Behavior of Zeta Potential of Silica Suspensions

Zeta potential is one of the most relevant parameters controlling the rheological behavior of ceramic suspensions. In this work, it was observed that for pH values below the isoelectric point (IEP), the positive value of zeta potential of water suspensions of α-quartz and α-cristobalite, experiences a sudden steep increase with the increase in specific surface area of the powders. For pH values above the IEP, the zeta potential values of crystalline forms of silica (α-quartz and α-cristobalite), get gradually more negative with the increase in pH. Conversely in the case of vitreous silica, for pH values above 6, there occurs a steep change towards more negative values of zeta potential than those presented by quartz and cristobalite. These findings have not yet been accounted for in the DLVO theory but may provide subsidies for better understanding of how to stabilize and destabilize crystalline and vitreous silica water suspensions.

Progress in nanoparticles characterization:Sizing and zeta potential measurement

Characterization of various nanoparticles is on the center stage in nanotechnology development. The subjects for nanoparticles characterization are focused on particle size and particle surface charge determinations. This article summarizes the latest development in particle size analysis using dynamic light scattering and surface charge determination using electrophoretic light scattering for nano-or even sub-nanoparticles in concentrated suspensions.

Influence of zeta potential on the flocculation of cyanobacteria cells using chitosan modified soil

Using chitosan modified soil to flocculate and sediment algal cells has been considered as a promising strategy to combat cyanobacteria blooms in natural waters. However, the flocculation efficiency often varies with algal cells with different zeta potential（ZP） attributed to different growth phases or water conditions. This article investigated the relationship between ZP of Microcystis aeruginosa and its influence to the flocculation efficiency using chitosan modified soil. Results suggested that the optimal removal efficiency was obtained when the ZP was between- 20.7 and- 6.7 m V with a removal efficiency of more than 80% in 30 min and large floc size of 〉 350 μm. When the algal cells were more negatively charged than- 20.7 m V, the effect of chitosan modified soil was depressed（〈 60%） due to the insufficient charge density of chitosan to neutralize and destabilize the algal suspension. When the algal cells were less negative than- 6.7 m V or even positively charged, a small floc size（〈 120 μm） was formed, which may be difficult to sink under natural water conditions. Therefore, manipulation of ZP provided a viable tool to improve the flocculation efficiency of chitosan modified soil and an important guidance for practical engineering of cyanobacteria bloom control.

Pristine point of zero charge (p.p.z.c.) and zeta potentials of boehmite’s nanolayer and nanofiber surfaces

The pristine point of zero charge(p.p.z.c)and zeta potential as a function of pH of boehmite oxide/hydroxide(α-Al_(2)O_(3)·H_(2)O)have been determined for three filter media.The active component in the first two filter media is boehmite nanofibers,only 2 nm in diameter and about 300 nm long.Boehmite nanofibers create high zeta potential(ζtrue≥46 mV)in aqueous solutions in the pH range of 3–8.The p.p.z.c.values were determined to be 11.60±0.15 for nanofibers grafted onto microglass fibers and 11.40±0.15 for agglomerated nanofibers.In the third filter media,a boehmite nanolayer in the form of monocrystalline oxide/hydroxide with a thickness of approximately 1.2 nm is electroadhesively deposited onto siliceous support material with large surface area of about 50 m^(2)/g,therefore forming a highly electropositive composite of boehmite nanolayer on the second highly electronegative solid.Boehmite’s oxide-hydroxide nanolayer surface creates high zeta potential(ζtrue≥50 mV)in aqueous solutions in the pH range of 3–8.The p.p.z.c.value was determined to be 11.38±0.15.The reported values are within accuracy,but they are much higher than the values reported in the literature.X-ray powder diffraction data were supplemented by microscopy,infrared spectroscopy in order to characterize fully synthetic boehmite surfaces.

Sphalerite/silica interaction:Zeta potential distribution measurement

An appropriate measurement is needed to control the calcium ion content and reduce the interaction among fine mineral particles.In this paper,the sphalerite/silica interactions were studied by Zeta potential measurements and a novel Zeta potential distribution（ZPD）measurement method in different concentrations of calcium ion solution.To study mineral surface molecular and atomic absorption states,energy dispersive spectroscopy（EDS） and scanning electron microscope（SEM） were used.Flotation reagent adsorbed on the mineral surface was analyzed by the interactions status.The results show that adsorption of flotation reagent is not conducive when the calcium ion concentration is high in the solution.Reducing the calcium ion concentration is the effective method to reduce particle interactions in the pulp.The specific method is that the appropriate amount of sodium carbonate is added into the gypsum-supersaturated solution.The minerals＇ interactions can be interpreted by measuring ZPD.

Zeta potential measurement on lithium lanthanum titanate nanoceramics

The zeta potential, isoelectric point, and agglomeration of Lio.sLao.sTiO3 （LLTO） nanoparticles dispersed in aqueous media at different ionic strengths have been studied. The zeta potential was determined from electrophoretic mobility measurements, according to Smoluchowski＇s equation, for Li0.5La0.5TiO3 suspen- sions in NaCl and KCI electrolytes with ionic strengths of 1, 10, and 100 mmol/dm3. The isoelectric point （IEP）, zeta potential （ζ）, and the agglomeration were shown to strongly depend on the ionic strength of the Li0.5La0.5TiO3 aqueous colloidal suspension in both NaCI and KCI electrolytes, which allows the deter- mination of the effects of environmental conditions for Lio.sLao.sTiO3 manipulation in aqueous colloidal systems. The suspensions of Li0.5La0.5TiO3 nanoparticles reach the IEP in the pH range 0f3-5. The （ of Li0.5La0.5TiO3 nanoparticles varied from positive to negative values with a pH increase, which allows for the control of the surface charge depending on the purpose. The pH range of 7-g and an ionic strength ≤1 mmol/dm3 are recommended as the most suitable conditions for both the LLTO colloidal shaping techniques application and the LLTO-based nanocomposite formation.

The impact of salinity,alkalinity and nanoparticle concentration on zeta-potential of sand minerals and their implication on sand production

The effect of brine salinity,cation type,pH,and produced sand on zeta potential(ZP)measurements with and without the presence of silica nanoparticles is investigated through pH measurement,static tests for sand and ZP measurements as well as Field Emission Scanning Electron Microscope(FESEM)analyses.Three important factors were investigated:composition of the injected brine,surface charge and pH.Their influence on stability of nanoparticles in the injected brine and amount of sand segregation was determined and the analysis of the new outcomes based on rock/brine ZP measurements was reported.The results show that the use of silica nanoparticles with high pH helps in preventing sand production and that pH has a main effect on the surface charge of the sand particle released,affecting the ZP of the solution.Nanoparticles can be active as a coating on sand grains and prevent sand segregation during water flooding.Divalent cations have been found to acquire a more substantial impact on neutralizing the negative charge of the sand particles than monovalent cations at the same concentration and pH conditions at 25℃.The value of ZP becomes of higher negative value with the decrease of brine salinity.The effectiveness of SiO_(2)nanoparticles is quite different for soft water and smart water.For soft water,the nanoparticles work more effective at pH higher than 8;and for smart water,the nanoparticles perform better at pH lower than 8.To reduce sand production with the use of silica nanoparticles,it is highly suggested to increase pH,as pH and sand production mechanisms were observed to be inversely related.

Experimental investigation of the effects of oil asphaltene content on CO_(2) foam stability in the presence of nanoparticles and sodium dodecyl sulfate

Foam stability tests were performed using sodium dodecyl sulfate(SDS)surfactant and SiO2 nanoparticles as foaming system at different asphaltene concentrations,and the half-life of CO_(2) foam was measured.The mechanism of foam stability reduction in the presence of asphaltene was analyzed by scanning electron microscope(SEM),UV adsorption spectrophotometric concentration measurement and Zeta potential measurement.When the mass ratio of synthetic oil to foam-formation suspension was 1:9 and the asphaltene mass fraction increased from 0 to 15%,the half-life of SDS-stabilized foams decreased from 751 s to 239 s,and the half-life of SDS/silica-stabilized foams decreased from 912 s to 298 s.When the mass ratio of synthetic oil to foam-formation suspension was 2:8 and the asphaltene mass fraction increased from 0 to 15%,the half-life of SDS-stabilized foams decreased from 526 s to 171 s,and the half-life of SDS/silica-stabilized foams decreased from 660 s to 205 s.In addition,due to asphaltene-SDS/silica interaction in the aqueous phase,the absolute value of Zeta potential decreases,and the surface charges of particles reduce,leading to the reduction of repulsive forces between two interfaces of thin liquid film,which in turn,damages the foam stability.

Carbon nanotubes as conducting support for potential Mn-oxide electrocatalysts： Influences of pre-treatment procedures

Different oxygen and nitrogen containing functional groups were created on the surface of the multiwalled carbon nanotubes. The multi-walled carbon nanotubes were treated in ultrasonic bath with sulfuric or nitric acid. Furthermore the surface texture was modified by increase of the roughness. In particular after treatment with the oxidizing nitric acid, in comparison to the H2SO4 or ultra-sonic treated samples,craters and edges are dominating the surface structures. Manganese oxide was deposited on the multiwalled carbon nanotubes by precipitation mechanism. Various manganese oxides are formed during the deposition process. The samples were characterized by elemental analysis, microscopy, thermal analysis,Raman spectroscopy, and by the zeta potential as well as X-ray diffraction measurements. It was shown that the deposited manganese oxides are stabilized rather by surface texture of the multi-walled carbon nanotubes than by created functional groups.

Creating burdock polysaccharide-oleanolic acid-ursolic acid nanoparticles to deliver enhanced anti-inflammatory effects:fabrication,structural characterization and property evaluation

This study explored the potential of polysaccharides from Actium lappa(ALPs)as natural wall materials for producing ALP-based nanoparticles to deliver poorly water-soluble oleanolic acid(OA)and ursolic acid(UA).Encapsulating OA+UA with ALPs(ALP:OA+UA,50:1;OA:UA,1:1)changed the crystalline nature to a more amorphous state through hydrogen bonding and involving O-H/C-O/O-C-O groups.ALP-OA/UA nanoparticles had a particle size and zeta potential(in water)of 199.1 nm/-7.15 mV,with a narrow unimodal size distribution,and excellent pH,salt solution,temperature and storage stability.Compared with ALPs,ALPOA/UA nanoparticles showed enhanced anti-inflammatory activity(especially at a dose of 100μg/mL)in a CuSO-induced zebrafish inflammation model via down-regulating the NF-κB signalling pathway and gene expression of associated transcription factors and cytokines(TNF-α,IL-1βand IL-8).Therefore,ALP-based nanoparticles are natural and anti-inflammatory carriers for hydrophobic bioactive molecules.

Impact of surface roughness,surface charge,and temperature on sandstone wettability alteration by nanoparticles

The wettability of rocks affects the balance between capillary and viscous forces during multiphase flow through porous media,which in turn determines the fluid displacement process governing the recovery of oil from subsurface formations.In this work,the mechanism of wettability reversal of aged synthetic sandstones by metal oxide nanoparticles(SiO_(2) and Al_(2)O_(3))was investigated with particular focus on the impact of surface roughness,zeta potential,and temperature.The synthetic surfaces were prepared from powders of Berea sandstone with known grain size ranges and their average roughness and roughness ratio were obtained from the 3D surface reconstruction of their microscope images.Each surface was subsequently aged in Permian crude oil to alter its wettability.For surfaces with larger grain sizes and lower surface roughness ratios,the lower capillary pressure allowed stronger oil/surface interactions,leading to enhanced oil-wetness.The wettability alteration effects of nanoparticles were then examined through real-time top view imaging and dynamic front view contact angle experiments.The negatively charged SiO_(2) nanoparticles rapidly reversed the sandstone wettability,indicating their potential applicability as wettability alteration agents.By contrast,the positively charged Al_(2)O_(3) counterpart caused no wettability reversal.The mechanism of wettability alteration was further studied by microscale interaction analyses and nanoscale transmission electron microscopy.Because nanoparticles were only a few nanometers large,the microscale roughness had a negligible effect on the wettability reversal.Instead,the combined effect of van der Waals dispersion forces and surface-charge-induced electrostatic forces were recognized as the two key factors affecting the wettability of sandstone particles.Such interactions may be curbed at elevated temperatures due to a decrease in the zeta potential and colloidal stability of the particles.