Properties Of Polymer Solutions Research Articles

An Investigation of the Factors Influencing the High Temperature Rheology of Polymers

Introduction: Nowadays, polymers, as an important application material in drilling engineering, have obvious advantages in solving the rock-carrying problem at the bottom of deep wells, and improving the drilling speed due to their excellent viscosity enhancement effect. Method: In this study, the effects of polymer type, concentration, shear time, electrolyte, and clay on the rheological properties of polymer solutions at high temperature and high pressure were investigated using a Fann 50SL rheometer. The experimental results showed that, except for the polymer additive amount and clay, the increase in shear time and the amount of salt both led to a decrease in the viscosity of the polymer solution, with 190°C as the critical temperature above which the viscosity decreased significantly. Results: The polymer solution containing formate showed higher viscosity retention during heating and then cooling compared to chlorides. The presence of clay enhances the reticulation of polymer molecules in the blend, which facilitates the carrying of rock cuttings at high temperatures. In addition, regression analyses showed that the increase in temperature resulted in an enhanced tendency for the polymer solution to evolve from a pseudoplastic to a Newtonian type. Conclusion: This research provides theoretical basis and data support for developing high-temperature polymers and formulating high-temperature drilling fluid systems.

Effects of Dye Addition on the Rheological Properties of Aqueous Polymer Solutions.

In many commercial applications, polymer-dye interactions are frequently encountered from food to wastewater treatment, and while shear rheology has been well characterized, the extensional properties are not well known. The extensional viscosity ηE and relaxation time λE are the extensional rheological parameters that provide valuable insights into how aqueous polymers respond during deformation, and this study investigated the effect of dyes on the extensional rheology of three different aqueous polymer solutions (e.g., anionic, cationic, and neutral) paired with two different dye salts (e.g., anionic and cationic) using drop pinch-off experiments. We have found that the influence of dyes on the pinch-off dynamics is complex but generally leads to a decrease in, for example, the apparent extensional relaxation time. We have utilized the dripping-onto-substrate method to probe the uniaxial deformation of widely used polymers such as xanthan gum (XG), poly(diallyldimethylammonium chloride) (PDADMAC), and poly(ethylene oxide) (PEO) as the anionic, cationic, and neutral polymers, respectively, paired with either fluorescein (Fl) or methylene blue (MB) as the anionic and cationic dyes, respectively. Polymer-dye pairs with opposite charges (e.g., XG-MB and PDADMAC-Fl) displayed a pronounced decrease in pinch-off times, but even PEO, which is a neutral polymer, resulted in decreased pinch-off times, which was restored by the addition of NaCl. The pinch-off times for the Boger fluid (mixture of poly(ethylene glycol) and PEO), however, were surprisingly uninfluenced by dyes. These results showed that not only did the small addition of dyes strongly decrease the polymer relaxation times, but the relative importance of the dye salts on the polymer pinch-off dynamics was also different from that of pure salts such as NaCl.

Application and Optimization of Rheological Mathematical Models in Preparation and Injection Process of Polymer Flooding

The impact of shear on the properties of polymer solutions is not fully accounted for in the simulation of conventional rheological models. To optimize the application of these mathematical models, the shear rheological characteristics of polyacrylamide at various concentrations were investigated under different shear rates and shear modes. The results indicate that pseudoplastic fluid polymers exhibit two distinct rheological characteristics within their "shear thinning" rate range. The critical shear rate at this threshold signifies the point at which shear stress begins to disrupt the structure of the polymer solution, resulting in a rheological curve that transitions from high to low shear rates without reverting back to a low-to-high state. The concentration of the solution has minimal effect on the critical shear rate of the polymer, which is primarily determined by the inherent properties of the polymer itself. The application of rheological models during preparation and injection processes can elucidate the effects of shear on polymers by analyzing changes in apparent viscosity. Furthermore, the rheological model following supercritical shear rates requires modifications to the consistency coefficient (K) and flow index (n) based on shear rheological data obtained from high to low shear rates.

Micro-PIV of viscoelastic fluid flow in microporous media

The present experimental investigation combines the bulk flow properties of polymer solutions and measurable rheological parameters as they flow through a distinctive micro-porous structure, with micro-PIV (micro-particle image velocimetry) to measure the velocity distribution and velocity fluctuations within individual pores of a novel porous glass structure. To investigate the effects of fluid elasticity at pore scale, aqueous solutions of a polyacrylamide (PAA) & polyethylene oxide (PEO) in the concentration range of 50–200 ppm, which were characterized in both shear and extensional flows using shear and capillary break-up extensional rheometers (CaBER) respectively, were used as working fluids. The velocity field measurement includes the velocity magnitude and fluctuation intensity in several different pores within the porous material across a Weissenberg number Wi range of approximately 0.01 to 1 for each of the test fluids. The global averaged fluctuation intensity increases with Wi but the critical value, which indicates the onset of significant unsteadiness (i.e. well above noise floor/Newtonian baseline) within the flow at pore scale gives an approximately constant value of Wi≈0.4, which is almost 40 times higher than the value that is observed in the pressure-drop measurements for the data to rise above the Newtonian base line. We therefore postulate that the enhanced pressure-drop behaviour of the bulk flow may not be due to local velocity fluctuations within the pores but due to mean flow effects, at least over a significant portion of the data (up to Wi≈0.4).

Longitudinal ultrasound measurements of polyethylene oxide across dilute to concentrated aqueous solutions

Measuring the properties of polymer solutions is crucial for understanding fundamental polymer physics. The longitudinal ultrasound measurement method offers a promising technique for characterizing these properties. In this study, we develop a mathematical model to correlate longitudinal ultrasonic signals with the material properties of polyethylene oxide (PEO) from dilute to concentrated aqueous solutions. After applying reflection and diffraction corrections, the accuracy of the measurement results improves to over 97 %. Our findings reveal a positive correlation between the speed of sound, density, and longitudinal modulus with the mass concentration of PEO. Additionally, ultrasonic relaxation analysis reveals that PEO solutions exhibit at least one relaxation process in the frequency range of 3–7 MHz, independent of concentration and molecular weight. Compared to dilute solutions, the relaxation amplitude in concentrated solutions is larger and accompanied by strong nonlinearity, attributed to conformational changes caused by molecular entanglement in concentrated solutions.

Anti-turbulent efficiency of oil-soluble polymer solutions and colloid systems flowing through cylindrical channel

Relevance. The use of anti-turbulent additives for transporting hydrocarbon liquids through main pipelines allows reducing significantly the energy consumption of pumping power stations. Aim. Comparative analysis of the anti-turbulent efficiency of high-molecular polymers and compositions of surfactants. Methods. Laboratory-scale experimentation aimed to study the flow of dilute polymer solutions and dispersed surfactant systems through a cylindrical channel of a turbulent rheometer. Results. The author has carried out the comparative experimental studies of the anti-turbulent efficiency of extremely dilute solutions of polymers and colloidal systems. The results were obtained that suggest a higher anti-turbulent efficiency of high-molecular-weight polymers compared to micellar surfactant systems. Solutions of high molecular weight polybutadiene and aluminum polyhydroxydicarboxylates in gasoline were used as samples for the experimental comparison of hydrodynamic efficiency. The paper describes the laboratory setup, on which the studies were carried out, and introduces the formulas used for quantitative calculations. The structure of polymer solutions and colloidal systems is considered and a theoretical explanation is given for the preferential use in industrial practice of high-molecular polymers in extremely low concentrations in real pipelines. It was found out that the mechanisms of degradation of antiturbulent properties of polymer solutions and dispersed surfactant systems are different. This is due to the difference in the structure of macromolar coils of polymer with an immobilized solvent and that of micelles from low molecular amphiphilic compounds. The paper introduces the arguments that explain the degradation of the antiturbulent properties of polymers not by the destruction of carbon-chain macromolecules, but by decomposition in a turbulent flow of the original large associates, consisting of a large number of chains, into individual and smaller macromolecular coils with an immobilized solvent.

Enhanced heat transfer in a two-dimensional serpentine micro-channel using elastic polymers

Elastic turbulence has emerged as a promising method to enhance heat transfer performance at the microscale. However, previous studies have mainly focused on the overall convective heat transfer performance in curved channels, overlooking the fact that the chaotic flow intensity varies along the streamline, leading to diverse local heat transfer characteristics. In this study, we systematically investigate the hydraulic and thermal properties of a dilute polymer solution under elastic turbulence conditions, where the inflow conditions exhibit a vanishing Reynolds number (Re) and high Weissenberg number (Wi), enabling a comprehensive understanding of the influence of polymers on the system. Through extensive direct numerical simulations using Rheotool, a two-dimensional curvilinear channel flow of an Oldroyd-B viscoelastic fluid is analyzed. By examining the variations of the friction factor and Nusselt number along the serpentine channel, we unveil both global and local characteristics of elastic turbulence. Based on the Wi value, we identify three distinct regimes. In the first regime (0<Wi≤3), we observe approximately 10% heat transfer enhancement accompanied by a roughly 5% reduction in the friction factor compared to laminar flow, known as polymer-induced thermal conductivity enhancement. In the second regime (3<Wi≤5), we observe a steep linear increase in heat transfer (around 30%) at the expense of up to 15% enhanced friction factor. Finally, in the fully developed elastic turbulence regime (Wi>5), we observe a remarkable heat transfer enhancement of up to 60% along with a reduced friction factor. The significant enhancement of heat transfer with increasing Wi can be attributed to the intensifying elastic instability resulting from the balance between normal stresses and streamlined curvatures.

On non-newtonian properties of polymer solutions during filtration through a porous medium

On non-newtonian properties of polymer solutions during filtration through a porous medium

Synergistic Effect of Opuntia ficus-indica Cladode mucilage on Physicochemical and Rheological properties of HPAM polymer solutions for EOR Application

This study focuses on the synthesis of a series of mixtures of a partially hydrolyzed polyacrylamide (HPAM), noted (H), and a cladode Opuntia ficus-indica mucilage (M). The main objective is to minimize the exclusive dependence of HPAM in the field of tertiary oil recovery, specifically in the process known as EOR.This study showed that a combination of 20% mucilage and 80% HPAM, for a total concentration of 800 ppm in solution, gives rheological performance equivalent to a solution of HPAM alone at 6000 ppm. The resulting mixture which is characterized by viscoelastic liquid behavior, exhibits remarkable flow and elasticity properties.This characteristic is considered favorable for extracting trapped oils from pores under effect of the normal stress. Spectral analysis revealed the presence of silica groups in the mixture, elements widely used in researchers in association with HPAM. Thermogravimetric analysis (TGA) demonstrated that mucilage decomposition only occurs at temperatures above 200 °C. As the main conclusion, all the physicochemical and rheological data argue in favor of the integration of mucilage in HPAM in order to minimize its concentration in Enhanced Oil Recovery (EOR) applications.

Molecular brushes with long polyfluorene backbones and polymethacrylic acid side chains: Luminescent properties and self‐organization in solutions

AbstractA series of molecular brushes with a polyfluorene (PF) backbone and polymethacrylic acid side chains of varying lengths were prepared by atom transfer radical polymerization. The structure and composition of the synthesized compounds were confirmed by 1H NMR and IR spectroscopy. Effect of the length of the backbone on spectral and conformational parameters of the macromolecules in solutions was analyzed. The grafting density of side chains was about 90%. Spectral methods have been used to determine the dependence of side chain grafting on the luminescent properties of polymer solutions, including quantum yields. It was shown that an optimal length of polymethacrylic acid side chains provides solubility of the polymer brushes. Solutions of PF‐graft‐polymethacrylic acid complexes with the model substance curcumin were investigated. It was established that the molecular brushes containing curcumin form monomolecular micelles. Molecular brushes with zinc phthalocyanine, potential systems for photodynamic, and photothermal therapy, were studied.

Rheological properties of polymer solutions and ways to improve the efficiency of development of high-viscosity oil fields in Uzbekistan

The results of experimental research on studying the filtration properties of polymer solutions and the mechanism of the displacement process in porous medium were presented in this article. The methodology of experimental studies in a specially designed laboratory setup is given. In the present work the rheological properties of polymer K-9 are considered. At the same time, the relaxation time of viscoelastic particles of K-9 polymer filtered in porous medium is experimentally found. Also, the results of experimental studies on oil displacement of fields with high content of asphaltene-resinous substances by polymer solutions on artificially created reservoir models to determine the optimal concentration of polymer solution and the size of the rim with the purpose of increasing oil recovery. Experimental studies on displacement of high-viscosity oils with a thickened water rim established that this method gives the greatest increase in water-free and ultimate oil recovery of reservoirs, within the range of change in the concentration of polymer solution 0.2-0.4%, with the size of the rim more than 70% of the oil saturated volume of the reservoir. Studies on displacement of high-viscosity oils by polymer solutions show that the use of this method of increasing oil recovery factor in practice is not always economically feasible, because of the need to ensure high injection pressures and high concentration of expensive polymer solution.

Phase behavior of colloidal nanoparticles and their enhancement effect on the rheological properties of polymer solutions and gels.

The interaction between nanoparticles and polymers has been of great interest in colloidal theory and novel materials. For example, the properties of polyacrylamide solutions and gels, which are usually used for conformance control and water shut-off in oilfields, can be improved with the addition of nanoparticles. This underlying mechanism and its applicability are investigated in this paper. A strong relationship between the phase behaviors of nanoparticles in polymer solutions and their enhancement effect on the rheology of the nanocomposite polymer solutions and gels was observed. Experiment results showed that the stability of nanoparticles was dependent on several factors, including pH, salinity, and polymer type. At neutral pH conditions, the tendency of the aggregation of nanoparticles was strengthened upon increasing the salinity, polymer concentration, and electronegativity of the polymers. Rheological measurements showed that nanoparticles could improve the viscosity of polymer solutions or the fracture stress of gels only if nanoparticles were aggregated in the corresponding systems. In addition, these rheological parameters significantly increased with increasing salinity and nanoparticle concentration. As a result, the mobility ratio of polymer solutions may be increased several times by the addition of nanoparticles. Referring to the gels, their rupture pressure gradient in the ideal model was also found to increase with nanoparticle concentration. In particular, if the nanoparticle concentration was sufficiently high (reaching 2%), the formed gels would not be destroyed by the injected water, but rather functionally act as a porous medium for permeation.

Parameter estimation on polymer solutions with fractional viscoelastic model

The rheological properties of polymer solutions are extremely complex and it leads to a specific power-law behavior in response to creep experiments, which can not be better characterized by the classical viscoelastic constitutive models. The renowned viscoelastic fluid models with fractional derivatives have shown astonishing advantages in characterizing the broad relaxation process of the multiple materials with power-law response behavior. In this paper, we use the fractional Maxwell constitutive model to simulate the power-law responses for several polymer solutions through experimental measuring, and better fitting results than classical models can be found.

ПОЛИМЕРЛІ ЕРІТІНДІЛЕРДІҢ РЕОЛОГИЯЛЫҚ ҚАСИЕТТЕРІН ЗЕРТТЕУ

Annotation. The long-term operation of the deposit, the alternation of reservoir zones with high and degraded filtration and capacitance properties due to the heterogeneity of the reservoir, the deformation of the development system due to downtime and inactivity of wells predetermined the selective movement of water through the most permeable layers. As practice shows, the widespread use of traditional flooding technology does not ensure the effective production of residual reserves from low-permeable and highly watered formations. Therefore, increasing the degree of oil extraction from the depths of the developed fields using effective methods of active impact on water-oil-saturated formations is an important scientific and technical task facing the oilmen of the republic. One of the most effective and promising methods of stabilizing oil production is physics-chemical technologies based on the use of injection of polymer compositions. The main purpose of injection of polymer compositions is to equalize the heterogeneity of productive layers by reducing the mobility of the displacing agent in highly conductive interlayers and increasing the coverage of the reservoir by flooding both in power and in stretch. As is known, the effectiveness of the use of technologies based on polymer solutions depends on their good selective filterability into zones with high water saturation, which allows creating water-insulating screens in the desired direction and to a sufficient depth. It is known that the effective use of polymer solutions depends on the influence of various factors: molecular weight, polymer concentration in solution, filtration rates, reservoir permeability, as well as such an important parameter as the rheological properties of polymer solutions. The study of the rheological properties of polymer solutions allows us to substantiate and propose for practical implementation effective integrated technologies for increasing oil recovery during the operation of the oil fields under consideration. In this work, the rheological properties of polyacrylamide, physical parameters, taking into account their physics-chemical properties, are studied. The influence of mineralization and water hardness on polymer solutions is considered. The issues of mechanical destruction of polymers have been studied. The degree of mechanical destruction of the polymer is estimated based on the results of the study of the rheological properties of the polymer sample.

Viscoelastic rheology of polymer solution probed by resonant thermal capillary fluctuation

We present a measurement of viscoelastic properties of polymer solutions using resonant thermal capillary fluctuations of the surface of a polymer solution droplet. The instantaneous deflection of a cantilever in contact with the drop surface allows for measuring the nanoscale thermal fluctuations of the interface. From the power spectral density of measured fluctuations, we determine the two components of the rheological (dynamic and elastic viscosity) response of the fluid. Our experimental results were compared with rheological measurements using a classical commercial rheometer. We find a good agreement between the two measurements. Our experiments allow to extend the range for dynamical measurements of rheological properties of the solutions up to 20 000 s−1. Furthermore, our method requires only a small volume of liquid (10 μl) to measure the viscosity and is thus suitable for measurements on precious liquids.

Linking surface tension to water polarization with a new hypothesis: The Ling-Damodaran Isotherm.

Studying aqueous solutions of complex (bio)polymers is essential from both theoretical and practical perspectives. To understand the principles that govern the properties of these solutions is pivotal for the study of biological processes, considering that the most distinguished components of the cells are polymers (proteins, nucleic acids). These macromolecular aqueous systems, known as colloids, has raise the interest of scientists in recent years. It is known that several physicochemical properties deviate from ideal behaviour in this kind of solutions and that the physical state of water is different compared to its pure state. Particularly, the surface tension of such mixtures often shows a peculiar profile at semi-dilute and concentrated conditions. Here, we joined the colloidal concept of water polarization (proposed in the Association-Induction Hypothesis) with Damodaran's formalism for surface tension to theoretically derive a compelling mathematical model that explains the behaviour of polymer solutions. We measured the surface tension and osmolarity of different polyethylene oxide solutions and we used the ACDAN fluorescence probe to assess the water dipolar relaxation (polarization) in these mixtures. As a proof of concept, we also studied the influence of these polymer solutions on lipid interfaces. Our isotherm model explains the experimental observations with a unifying view that correlates with other measured properties, such as osmolarity and water dipolar relaxation. This provides a link between interfacial and bulk physicochemical properties of polymer solutions, also giving a new framework for studying the interaction of colloidal systems with lipid membranes interfaces.

Temperature-mediated diffusion of nanoparticles in semidilute polymer solutions.

The temperature is often a critical factor affecting the diffusion of nanoparticles in complex physiological media, but its specific effects are still to be fully understood. Here, we constructed a temperature-regulated model of semidilute polymer solution and experimentally investigated the temperature-mediated diffusion of nanoparticles using the particle tracking method. By examining the ensemble-averaged mean square displacements (MSDs), we found that the MSD grows gradually as the temperature increases while the transition time from sublinear to linear stage in MSD decreases. Meanwhile, the temperature-dependent measured diffusivity of the nanoparticles shows an exponential growth. We revealed that these temperature-mediated changes are determined by the composite effect of the macroscale property of polymer solution and the microscale dynamics of polymer chain as well as nanoparticles. Furthermore, the measured non-Gaussian displacement probability distributions were found to exhibit non-Gaussian fat tails, and the tailed distribution is enhanced as the temperature increases. The non-Gaussianity was calculated and found to vary in the same trend with the tailed distribution, suggesting the occurrence of hopping events. This temperature-mediated non-Gaussian feature validates the recent theory of thermally induced activated hopping. Our results highlight the temperature-mediated changes in diffusive transport of nanoparticles in polymer solutions and may provide the possible strategy to improve drug delivery in physiological media.

Multi-scale modelling of dilute viscoelastic liquids: Atomistic to mesoscale mapping of polymer solutions

A framework predicting the rheological (storage and loss moduli, first normal stress coefficient, and relaxation time) and transport (viscosity, diffusivity) properties of non-Newtonian dilute polymer solutions at mesoscales (e.g. ∼ns to μs) from the atomistic-scale molecular behaviour is presented. More specifically, the rheological behaviour differences of OCP and PMA polymer solutions in PAO-2 oil are simulated using both atomistic molecular dynamics (MD) and many-body dissipative particle dynamics (mDPD) within a temperature range of 313–373 K. The simulation methodology described is able to distinguish itself from the standard DPD model by accurately reproducing the shear-thinning with high sensitivity, as seen in the atomistic MD simulations at high shear rates (e.g. 108−1013 s−1). It is shown that the model is well-suited to compute properties such as first normal stress differences and relaxation times that are difficult to estimate at atomistic scales due to the low signal-to-noise ratio. Moreover, the Schmidt numbers (>103) are predicted with high accuracy when compared with the values from atomistic-scale simulations. The proposed model is able to predict relaxation times of dilute polymer mixtures that are difficult to be obtained using state-of-the-art rheometers. Finally, it is found that the terminal relaxation time of PMA polymer chain does not vary monotonically as a function of temperature, unlike in the case of OCP; this is significant for describing viscoelastic behaviour at macroscales where satisfactory constitutive equations are not available.

Morphological and Wettability Evaluation of Electrospun Polivinyl Alcohol (PVA) Nanofiber Membrane for Wound Dressing Application

Many researches have focused on producing electrospun nanofiber membranes (ENMs) aiming to speed up physiological events of wound healing. However, it is still a challenge to fabricate functional ENMs using electrospinning technique, taken into account various factors that may affect the fibers diameter such as polymer solution properties, electrospinning parameters and ambient conditions. This study aimed to evaluate the combined electrospinning process parameters and characterize the morphology and wettability of the electrospun polyvinyl alcohol (PVA) nanofiber membranes produced. Process parameters that were optimized include applied voltage, flow rate, and distance to collector. The fabrication of PVA nanofiber membranes was done at 21 kV, 2 mL/h and 10 cm after optimization. Surface morphology and fiber diameter were analyzed using a scanning electron microscope (SEM). The water contact angle was used to analyze wettability. Electrospun PVA nanofiber membranes showed continuous random fiber, no bead defect, hydrophilic surface and average fiber diameters between 265 ± 86 nm and 281 ± 90 nm. Smaller fiber diameter between 200-700 nm can enhance cell migration. It is suggested from this study that the optimized parameters have successfully produced electrospun PVA nanofiber membranes with suitable fiber diameter for cell migration and can direct cell response, thus can be applied as a wound dressing material.

Synthesis and molecular structure of highly compact star-like poly(methyl methacrylate) and poly(butyl methacrylate)

Poly(methyl methacrylate) and poly(n-butyl methacrylate) highly dense star-like polymers with a varied number and length of arms were prepared by the arm-first group transfer polymerization. The work is focused on the detailed characterization of the molecular structure and dilute solution properties of star-like polymers. The refractive index increment of the star-like polymers was compared with that of corresponding linear homopolymers. The prepared polymers were characterized by size exclusion chromatography coupled with a multi-angle light scattering detector and an online viscometer. Except for the commonly used molar mass, root mean square radius, and intrinsic viscosity, the obtained data also allowed the determination of the distribution of the arms per molecule, the calculation of the average number of arms per molecule, and the determination of the molar mass dependency of the draining factor. The relation between the number of arms per molecule and molar mass was estimated using various theoretical equations and compared with the true values obtained by the division of the slice molar mass by the molar mass of arms.