Steady Shear Experiments Research Articles

Shear thickening behaviour of polyborosiloxane

Polyborosiloxane (PBS) is often referred to as a “shear thickening/stiffening gel” or “dilatant compound”, sometimes actually meaning an increase in modulus with frequency/strain rate rather than the rheological definition of “dilatant compound”, i.e. an increase in viscosity with shear rate. The shear behaviour of bulk PBS and PBS solution has been studied here by steady shear experiments, and it is observed that PBS exhibits shear thickening behaviour only under certain conditions. The shear behaviour of bulk PBS depends on the degree of reaction of the PBS (i.e. the content of B in the PBS). For PBS solution, the shear behaviour is influenced by the concentration of the solution and the type of solvent (with or without oxygen atom in the solvent). The shear behaviour of PBS systems is related to shear induced structural changes, where the formation of new elastically active B:O dynamic dative bonds (interchain cross-linking) contributes to shear thickening.

Rheological and Micro-Rheological Properties of Chicory Inulin Gels.

As a soluble fiber, inulin is present in many plants and has many applications in food and non-food products. In this work, we investigated the rheological properties of inulin dispersions at seven concentrations. The linear viscoelastic properties of inulin were determined using a conventional mechanical rheometer. At 25 wt%, inulin exhibited fluid-like viscoelastic liquid behavior. However, when concentrations were ≥27.5 wt%, inulin exhibited gel-like viscoelastic properties. The viscoelastic properties (moduli and viscosities) increased with increasing inulin concentration. The high-frequency linear rheological properties of inulin were also investigated using the modern light scattering technique, diffusion wave spectroscopy (DWS). The diffusion wave spectroscopy (DWS) measurements showed the amplitude of complex moduli (|G*(ω)|) of inulin gels (≥27.5 wt%) to be proportional to ½ power law of the frequency, which suggests inulin gels behave similarly to flexible polymers. The non-linear steady shear experiments demonstrated that inulin exhibited shear-thinning behavior that was well fitted by a power law constitutive model. The trend of the power law exponent from the experiments indicated that the shear-thinning extent for inulin was greater as the inulin concentration increased. The results of this work indicated that the properties of inulin gel can be manipulated by altering its concentration. Therefore, the desired inulin product can be designed accordingly. These results can be used to direct further food and non-food applications, such as wound healing materials for inulin gels.

The role of rolling resistance in the rheology of wizarding quidditch ball suspensions

To elucidate the effect of particle shape on the rheology of a dense, viscous suspension of frictional, non-Brownian particles, experimental measurements are presented for suspensions of polystyrene particles with different shapes in the same solvent. The first suspension is made of spheres whereas the particles which compose the second suspension are globular but with flattened faces. We present results from steady shear and shear-reversal rheological experiments for the two suspensions over a wide range of stresses in the viscous regime. Notably, we show that the rheology of the two suspensions is characterised by a shear-thinning behaviour, which is stronger in the case of the suspension of globular particles. Since the shear-reversal experiments indicate an absence of adhesive particle interactions, we attribute the shear thinning to a sliding friction coefficient which varies with stress as has been observed previously for systems similar to the first suspension. We observe that the viscosity of the two suspensions is similar at high shear stress where small sliding friction facilitates particle relative motion due to sliding. At lower shear stress, however, the sliding friction is expected to increase and the particle relative motion would be associated with rolling. The globular particles attain a higher viscosity at low shear stress than the spherical particles. We attribute this difference to a shape-induced resistance to particle rolling that is enhanced by the flattened faces. Image analysis is employed to identify features of the particle geometry that contribute to the resistance to rolling. It is shown that the apparent rolling friction coefficients inferred from the rheology are intermediate between the apparent dynamic and static rolling friction coefficients predicted on the basis of the image analysis. All three rolling resistance estimates are larger for the globular particles with flat faces than for the spherical particles and we argue that this difference yields the stronger shear thinning of the globular particle suspension.

Microstructural and thermodynamic characterization of wormlike micelles formed by polydisperse ionic surfactant solutions.

For industrial applications of self-assembled wormlike micelles, measurement and characterization of a micellar material's microstructure and rheology are paramount for the development and deployment of new high-performing and cost-effective formulations. Within this workflow, there are significant bottlenecks associated with experimental delays and a lack of transferability of results from one chemistry to another. In this work, we outline a process to predict microscopic and thermodynamic characteristics of wormlike micelles directly from rheological data by combining a more robust and efficient fitting algorithm with a recently published constitutive model called the Toy Shuffling model [J. D. Peterson and M. E. Cates, J. Rheol. 64, 1465-1496 (2020) and J. D. Peterson and M. E. Cates, J. Rheol. 65, 633-662 (2021)]. To support this work, linear rheology measurements were taken for 143 samples comprising a common base formulation of commercial sodium lauryl ether sulfate, cocamidopropyl betaine, and salt (NaCl). The steady state zero shear viscosity evident in linear rheology was measured in duplicate via direct steady and oscillatory shear experiments. Fitting the collected data to the model, we found trends in the microstructural and thermodynamic characteristics that agree with molecular dynamics simulations. These trends validate our new perspective on the parameters that inform the study of the relationship between chemical formulation and rheology. This work, when implemented at scale, can potentially be used to inform and test strategies for predicting self-assembled micellar structures based on chemical formulation.

Rheology guiding the design and printability of aqueous colloidal composites for additive manufacturing

AbstractVat photopolymerization (VP) and direct ink write (DIW) additive manufacturing (AM) provide complex geometries with precise spatial control employing a vast array of photo‐reactive polymeric systems. Although VP is recognized for superior resolution and surface finish, DIW provides versatility for higher viscosity systems. However, each AM platform presents specific rheological requirements that are essential for successful 3D printing. First, viscosity requirements constrain VP polymeric materials to viscosities below 10 Pa s. Thus, this requirement presents a challenging paradox that must be overcome to attain the physical performance of high molecular weight polymers while maintaining suitable viscosities for VP polymeric materials. Second, the necessary rheological complexity that is required for DIW pastes requires additional rheological measurements to ensure desirable thixotropic behavior. This manuscript describes the importance of rheological measurements when designing polymeric latexes for AM. Latexes effectively decouple the dependency of viscosity on molecular weight, thus enabling high molecular weight polymers with low viscosities. Photo‐crosslinking of water‐soluble monomers and telechelic oligomeric diacrylates in the presence of the latex enables the fabrication of a scaffold, which is restricted to the continuous aqueous phase and effectively surrounds the latex nanoparticles enabling the printing of otherwise inaccessible high molecular weight polymers. Rheological testing, including both steady and oscillatory shear experiments, provides insights into system properties and provides predictability for successful printing. This perspective article aims to provide an understanding of both chemical functionality (photo‐ and thermal‐reactivity) and rheological response and their importance for the successful design and evaluation of VP and DIW processable latex formulations.

Effect of specific surface area on the rheological properties of graphene nanoplatelet/poly(ethylene oxide) composites

The rheological properties of poly(ethylene oxide) containing graphene nanoplatelets (GNPs) having different specific surface areas (SSAs) are studied using steady shear and small amplitude oscillatory shear experiments. A series of GNPs having SSAs ranging from 175 ± 5 to 430 ± 13 m2/g was prepared using a thermomechanical exfoliation process. The complex viscosity, moduli, and yield stress of the composites increase with SSA, whereas electrical and rheological percolation threshold concentrations decrease, suggesting that higher SSAs promote filler network formation. Modeling of small amplitude oscillatory shear data using a two-phase model confirms that hydrodynamic effects dominate at low concentrations below 8 wt. %, where the particles are noninteracting. At higher concentrations, the response is dominated by filler-phase contributions. We demonstrate that the two-phase model parameters can be used to track the exfoliation of graphite into GNPs. Fitting of rheological percolation curves using Utracki and Lyngaae–Jørgensen models at low concentrations (noninteracting regime) resulted in aspect ratios between 19 and 76. At high concentrations (interacting particles), the aspect ratios determined by the Krieger–Daugherty model ranged between 5 and 24 due to aggregation. The highest aspect ratios (defined as the ratio of major dimension to minor dimension) were associated with GNPs that had the highest SSA of 430 m2/g. Strain sweeps revealed that the critical strain for the onset of nonlinear viscoelasticity scaled with SSA above the percolation threshold. The scaling relationships of the critical strain and storage modulus with volume fraction were used to infer the fractal dimensions of filler networks.

Viscoelastic properties of pNIPAM-hydrogels: A mode-coupling theory study

We investigate the viscoelastic properties of poly(N-isopropylacrylamide) (pNIPAM) hydrogels cross-linked with glutaraldehyde by means of small amplitude oscillatory and steady shear experiments in dependence on the frequency and shear rate. These properties are strongly influenced by the ratio of monomer and glutaraldehyde as a cross-linker. Due to the thermosensitivity of pNIPAM, the rheological properties of these hydrogels can be tuned by the temperature as an external stimulus. The experimentally obtained viscosities and linear viscoelastic moduli are analyzed by a schematic mode-coupling ansatz employing a rescaled F12-model.

Viscoelastic Characterization of Corn Starch Paste: (I) The First Normal Stress Difference of a Cross-Linked Waxy Corn Starch Paste with Sucrose

Experimental viscoelastic data and the corresponding theoretical analysis of corn starch paste in the past 30 years indicate an evident deficiency of the viscoelastic characterization of the paste. The purposes of the study are to check the capability of a recent model on describing the viscoelasticity of the paste and to improve the viscoelastic analysis. The linear viscoelastic property; the steady shear viscosity and the first normal stress difference (N1) of a cross-linked waxy corn starch paste mixed with sucrose experimentally reported in 2003 were characterized with a structuralized viscoelastic constitutive equation in the present paper. The structuralized parameter f in the equation was obtained using the viscosities in the dynamic and steady shear experiment. Both a power law strain model and a linear strain model were proposed to describe the normal component in the strain matrix. Three kinds of viscoelastic properties of the paste can be described well with the structuralized equation. Both the power law and the linear strain model can yield reasonable calculations of N1. The maximum deviation of N1 calculated by two strain models is about 10%. The theoretical model adopted is available for describing the complex viscoelastic behaviors of corn starch paste usually appearing in the processing of corn starch.

Prediction of the viscoelastic properties of a cetyl pyridinium chloride/sodium salicylate micellar solution: (I) characterization

The characterization capability of constitutive equation on the viscoelastic property of micellar solution was checked in this study. A modified viscoelastic model was employed here to express the viscoelastic properties of a cetyl pyridinium chloride/sodium salicylate (CPyCl/NaSal) wormlike micellar solution at 22 °C that was experimentally obtained in 2010. The relaxation spectrum of the CPyCl/NaSal solution was fitted using the dynamic frequency sweep, the parameter in the Papanastasiou-Scriven-Macosko damping function was obtained using stress relaxation in step strain, the structuralized parameter f in the model was obtained using the steady shear stress, and the parameter ζ was obtained using the stress growth in the shear startup experiment. Afterwards, the first normal stress difference of the solution in the steady shear experiment was predicted. The study clearly shows improvement in the calculated viscoelastic properties of the micellar solution compared with those obtained by the Vasquez-Cook-Mckinley model, such as steady shear stress.

Rheological Response of Polylactic Acid Dispersions in Water with Xanthan Gum.

In this work, the rheological behavior of stable poly(lactic acid) (PLA) dispersions in water, intended for coating applications, was investigated. The newly prepared dispersion consists of PLA particles with an average diameter of 222 ± 2 nm based on dynamic light scattering (DLS) and scanning electron microscopy (SEM) analyses, at concentrations varying in the 5–22 wt % range. Xanthan gum (XG), a bacterial polysaccharide, was used as a thickening agent to modulate the viscosity of the formulations. The rheological properties of the PLA dispersions with different XG and PLA contents were studied in steady shear, amplitude sweep, and frequency sweep experiments. Under steady shear conditions, the viscosity of all the formulations showed a shear-thinning behavior similar to XG solutions in the whole investigated 1–1000 s–1 range, with values dependent on both PLA particles and XG concentrations. Amplitude and frequency sweep data revealed a weak-gel behavior except in the case of the most diluted sample, with moduli dependent on both PLA and XG contents. A unified scaling parameter was identified in the volume fraction (ϕ) of the PLA particles, calculated by considering the dependence of the continuous phase density on the XG concentration. Accordingly, a master curve at different volume fractions was built using the time–concentration–superposition approach. The master curve describes the rheological response of the system over a wider frequency window than the experimentally accessible one and reveals the presence of a superimposed β relaxation process in the high-frequency region.

Characterization of Structural and Physicochemical Properties of an Exopolysaccharide Produced by Enterococcus sp. F2 From Fermented Soya Beans.

The present study sought to isolate a novel exopolysaccharide (EPS-F2) from Enterococcus sp. F2 through ethanol precipitation, anion-exchange, and gel-filtration chromatography and characterize the physicochemical properties by spectral techniques. EPS-F2 was identified as a neutral homo-exopolysaccharide composed of only glucose with a high molecular weight of 1.108 × 108 g/mol. It contained →6)-α-D-Glcp-(1→ linkage in the main chain and →3, 6)-α-D-Glcp-(1→ branch chain). Moreover, EPS-F2 possessed excellent thermal stability (266.6°C), water holding capacity (882.5%), oil holding capacity (1867.76%), and emulsifying activity against various edible oils. The steady shear experiments exhibited stable pseudo plasticity under various conditions (concentrations, temperatures, and pHs). The dynamic oscillatory measurements revealed that EPS-F2 showed a liquid-like behavior at a low concentration (2.5%), while a solid-like behavior at high concentrations (3.0 and 3.5%). Overall, these results suggest that EPS-F2 could be a potential alternative source of functional additives and ingredients and be applied in food industries.

Polyacrylamide Grafted Xanthan: Microwave-Assisted Synthesis and Rheological Behavior for Polymer Flooding.

Application of polymer-flooding systems in secondary and tertiary oil recovery represents a real challenge for oil industry. In this work, our main objective is to explore possibilities of making use of xanthan-g-polyacrylamide for polymer flooding in a particular Devonian oilfield of medium salinity. The graft polymer was synthesized by using microwave-assisted graft copolymerization reaction of acrylamide on xanthan. The synthesized copolymer with optimized grafting parameters has been characterized by Infrared Spectroscopy and Thermal Analysis (DSC). Rheological analysis by steady shear and oscillatory flow experiments have been subsequently performed for xanthan and grafted xanthan under reservoir conditions. In steady shear, as expected the grafted polymer solutions flow as shear-thinning materials and apparent viscosity showed good fits with Cross’s model. The viscosity losses due to salinity or temperature are more controlled for the grafted xanthan compared to pristine xanthan. When the grafted polymer concentration is increased to 2000 ppm the losses were halved. In oscillatory shear, the copolymer solutions followed a global behavior of semi-dilute entangled systems; furthermore, all dynamic properties were influenced by the brine salinity. Compared to xanthan, the elastic properties of xanthan-g-polyacrylamide solutions have been significantly improved in saline media and the losses in elasticity of grafted polymer solutions are lower.

Rheological characterization of CNC-CTAB network below and above critical micelle concentration (CMC)

The network of Cellulose Nanocrystal (CNC) suspension is explored below and above the critical micelle concentration (CMC), in the presence of cetyltrimethylammonium bromide (CTAB) with a positively charged head using TEM imaging and rheological characterization. CNC-CTAB gels show shear thinning behavior, complex relationship between strain amplitudes and CTAB concentration, diminishing thixotropic behavior as a function of CTAB and single and two yielding stress maxima as a function of CTAB, resulting from different microstructure below and above the critical Micelle Concentration (CMC) of CTAB. Comparing the flow curves of CNC-CTAB suspension/gel revealed the role played by CTAB content, CNC concentration and sonication energy in strengthening of the network. We analyzed and obtained yield stress from steady shear, creep testing and oscillatory experiments and compared them.

Rheological and emulsifying properties of an exopolysaccharide produced by potential probiotic Leuconostoc citreum-BMS strain

EPS-BMS, is to our knowledge, the first high molecular weight exopolysaccharide from potential probiotic Leuconostoc citreum-BMS strain that consists on a mixture of α-(1,6)-dextran branched at the third position and β-(2,6)-levan. This sample exhibited interesting rheological and emulsifying properties under different conditions. Steady shear experiments proved that EPS-BMS had a pseudoplastic behavior without thixotropic properties. Interestingly, pseudoplasticity was maintained even under stress conditions of temperature, pH and salts, which could provide some sensory properties for food products such as mouth feel. Dynamic oscillatory measurements reflected a liquid-like behavior of the sample regardless of the studied EPS concentration, pH, temperature and ionic force. Results related to the emulsifying as well as interfacial properties showed that EPS-BMS had great potential to be applied as emulsifier and/or emulsion stabilizer in both neutral and acidic conditions. Based on the properties reported in this work, EPS-BMS could be potentially applied in the food industry.

Yielding of cellulose nanocrystal suspensions in the presence of electrolytes

The rheological properties and yielding behavior of 1 wt. % aqueous sulfonated cellulose nanocrystals (CNCs) in the presence of monovalent (Na+) ions have been investigated. The introduction of more than 20 mM NaCl to the system causes aggregation of neutralized CNCs and leads to the formation of self-similar clusters, which grow in size until they form a three-dimensional network. In the present work, we report a comprehensive study of nonlinear rheology and yielding behavior of CNC/salt gels in steady shear and oscillatory experiments. Two yield stresses have been determined. The first yield stress at low shear rates is attributed to the disconnected CNC clusters as a result of bond breakage. The second yield point occurs at higher shear rates, and it is related to the deformation of clusters, where individual nanorods are nearly separated and dispersed. The existence of these two yield stresses has been identified in both steady-shear scans (high to low and low to high) as well as oscillatory experiments, resulting in consistent results.

Characterizing the rheology, slip, and velocity profiles of lamellar gel networks

The authors report the rheology and shear flow velocity profiles of pseudo-ternary “lamellar gel networks” commonly found in cosmetic emulsions such as creams, lotions, and hair conditioners, consisting of the cationic surfactant behentrimonium methosulfate, a fatty alcohol mixture of cetyl and stearyl alcohol, and water at surfactant/fatty alcohol mole fractions ranging from 0.1 to 0.6 and water mass fractions of 85%–97%. The high shear-thinning viscosity shows hysteresis in up- and down-ramps of the shear rate, with the gel “remembering” its highest shear for around 12 h before it heals and recovers its original viscosity. These materials exhibit rheological signatures characteristic of a soft glassy material (as described by the soft glassy rheology model) such as shear hysteresis, inhomogeneous velocity gradient, a solidlike creep response, power-law stress decay in step strain experiments, and high storage modulus relative to loss modulus over a wide range of frequencies, confirming its nearly elastic response for small deformations. Using particle image velocimetry (PIV) in steady shear experiments, a transition from a linear velocity profile to a pluglike profile was observed at shear rates above around 0.01 s−1. PIV also revealed macroscopic inhomogeneities including the development of fracture planes and shear bands, with rheology becoming gap-dependent and displaying some characteristics of solidlike friction.

GO CaBER: Capillary breakup and steady-shear experiments on aqueous graphene oxide (GO) suspensions

Aqueous solutions of graphene oxide (GO) with a very large average flake aspect ratio, AR = O ( 10 4 ), are probed using capillary breakup experiments and shear rheological measurements for concentrations up to ϕ = 0.4 vol . %. GO, a chemically oxidized sheet of graphene that we obtained from graphite exfoliation, is suspended in distilled water to produce solutions with volume concentrations spanning 0.02 ≤ ϕ ≤ 0.4 vol . %. For concentrations between 0.1 ≤ ϕ ≤ 0.4 vol . %, the apparent shear yield stress, τ y (determined from creep tests), scales with concentration following a power-law relationship with exponent ∼ 2.2. Using capillary breakup extensional rheometry (CaBER), we demonstrate that for concentrations ϕ ≳ 0.1 vol . %, aqueous GO solutions exhibit power-law fluid behavior in uniaxial elongation. The deformation-rate-dependent transient Trouton ratio over the range where the deformation rates match in shear and capillary breakup experiments is independent of the deformation rate, but inversely proportional to the volume concentration with all values exceeding 3. An attempt is made to estimate the apparent elongational yield stress (for ϕ ≥ 0.3 vol . %) by using the Laplace pressure within the fluid filament as its surrogate, and we find that in the strain rate regime that we can observe, the apparent elongational yield stress, τ y , e, is not 3 times the shear yield stress, i.e., for our aqueous GO solutions, we are not able to observe agreement with the von Mises plasticity criterion. GO samples at a given concentration probed in capillary breakup extensional rheology experiments under different protocols, i.e., slow-retraction opposed to step-stretch, exhibited different responses confirming that GO is highly sensitive to the deformation history; however, they still exhibit power-law fluid behavior even given the different initial conditions. Although slightly limited in our ability to quantify the extension-thinning yield-stress-like behavior of aqueous GO in uniaxial elongational flow by the fact that we cannot prescribe the strain rates in CaBER experiments, we demonstrated that even a very small amount of GO flakes can significantly alter the shear rheology and the pinch-off dynamics of a liquid bridge in comparison to Newtonian fluids of equivalent shear viscosity.Aqueous solutions of graphene oxide (GO) with a very large average flake aspect ratio, AR = O ( 10 4 ), are probed using capillary breakup experiments and shear rheological measurements for concentrations up to ϕ = 0.4 vol . %. GO, a chemically oxidized sheet of graphene that we obtained from graphite exfoliation, is suspended in distilled water to produce solutions with volume concentrations spanning 0.02 ≤ ϕ ≤ 0.4 vol . %. For concentrations between 0.1 ≤ ϕ ≤ 0.4 vol . %, the apparent shear yield stress, τ y (determined from creep tests), scales with concentration following a power-law relationship with exponent ∼ 2.2. Using capillary breakup extensional rheometry (CaBER), we demonstrate that for concentrations ϕ ≳ 0.1 vol . %, aqueous GO solutions exhibit power-law fluid behavior in uniaxial elongation. The deformation-rate-dependent transient Trouton ratio over the range where the deformation rates match in shear and capillary breakup experiments is independent of the d...

Measurements of human blood viscoelasticity and thixotropy under steady and transient shear and constitutive modeling thereof

New in vitro measurements from two human donors for both steady and transient hemorheology are presented that are particularly suited for testing thixotropic and viscoelastic models for human blood and are made available to the community along with the relevant blood physiology. This more complete data set is analyzed within the context of recent thixo-elasto-visco-plastic models, and we improve upon the Horner-Armstrong-Wagner-Beris (HAWB) model to better model transient hemorheology. The improved model features an additional viscoelastic equation for the red blood cell rouleaux within blood, along with simplifications to the structure kinetics equation. The resulting model is fit to additional experimental data on human whole blood for a step shear change and steady shear experiments, and the corresponding parameter values are used to predict oscillatory shear moduli, transient large amplitude oscillatory shear, and unidirectional large amplitude oscillatory shear data. The modified HAWB model shows significant improvement in fitting and predicting the experimental data. Specifically, a significant overshoot is captured in step shear changes from a low shear rate to a moderate shear rate, and a plateau for the storage modulus is observed at low frequencies. Highly nonlinear behavior is observed for the third harmonic in unidirectional large amplitude oscillatory shear in the form of multiple extremum separated widely in frequency, which can be identified with the two dominant mechanisms for generating viscoelasticity in human blood, namely, rouleaux structuring and red blood cell deformation. We also discuss the potential applications and difficulties associated with the constitutive modeling of transient blood rheology and provide insight into microstructural sources of the stress contributions to the bulk flow behavior.New in vitro measurements from two human donors for both steady and transient hemorheology are presented that are particularly suited for testing thixotropic and viscoelastic models for human blood and are made available to the community along with the relevant blood physiology. This more complete data set is analyzed within the context of recent thixo-elasto-visco-plastic models, and we improve upon the Horner-Armstrong-Wagner-Beris (HAWB) model to better model transient hemorheology. The improved model features an additional viscoelastic equation for the red blood cell rouleaux within blood, along with simplifications to the structure kinetics equation. The resulting model is fit to additional experimental data on human whole blood for a step shear change and steady shear experiments, and the corresponding parameter values are used to predict oscillatory shear moduli, transient large amplitude oscillatory shear, and unidirectional large amplitude oscillatory shear data. The modified HAWB model shows sig...

Molecular Morphology and Viscoelasticity of ASP Solution under the Action of a Different Medium Injection Tool.

In order to improve the oil displacement effect of alkali/surfactant/polymer (ASP) solution in low-permeability oil layers, Daqing Oilfield has proposed a separate injection technology. The objective of separate injection technology is to reduce the viscosity of ASP solution through a different medium injection tool and increase the injection amount of ASP solution in low permeability oil layer, thus improving the oil displacement effect. In order to study the effect of the different medium injection tool on ASP solution, SEM is used to observe the changes in molecular micromorphology before and after the ASP solution flows through the tool. Then, the influence of the tool on viscosity and the first normal stress difference of the solution are studied through static shear experiments. Finally, the storage and loss modulus of the solution are measured through dynamic mechanical experiments and the relaxation time and zero shear viscosity of the solution are verified and compared. The results show that molecular chains are obviously broken and the grid structure is destroyed after the ASP solution is acted on by the different medium injection tool. The viscosity and elasticity of ASP solution decrease, and the influence degree of the different medium injection tool on viscosity is greater than elasticity. The results of the steady shear experiment and dynamic mechanics experiment are consistent. Therefore, the different medium injection tool can achieve the purpose of use, which is conducive to the injection of displacement fluid into low-permeability oil layers and enhance the recovery ratio.

Oscillatory and Steady Shear Rheology of Model Hydrophobically Modified Ethoxylated Urethane-Thickened Waterborne Paints.

Hydrophobically modified ethoxylated urethane (HEUR) thickeners are widely used as rheology modifiers for waterborne paints. Although the rheology of HEUR solutions in water is fairly well-understood, their impact on the rheology of waterborne latex/pigment suspensions (formulated paints) is more complicated. We study the shear rheology of model HEUR/latex/TiO2 suspensions in water and investigate the dependence of both oscillatory and steady shear behaviors on the strength of the HEUR hydrophobes. We observe that in both oscillatory and steady shear experiments, rheological curves could be shifted onto a single master curve, demonstrating a "time-hydrophobe superposition". We also note that the oscillatory shear behavior exhibits a power-law spectrum of relaxation times, unlike the single-Maxwellian behavior of pure HEUR solutions. On the basis of these results and earlier experimental and theoretical findings, we propose that the rheology of the HEUR-thickened latex/TiO2 suspensions is mainly determined by the transient network of HEUR-bridged latex particles, with a broad distribution of the characteristic lifetimes of the bridge. The model is found to be in good qualitative and semiquantitative agreement with the experiments for both steady shear and oscillatory shear.