Increase In Fraction Research Articles

The noteworthy tensile plasticity and strength of CoFeSiB metallic glass fiber reinforced epoxy composites

AbstractMetallic glass fibers have high strength, poor plasticity and low Young's modulus. In this study, it was used as a reinforcement to prepare metallic glass fiber reinforced epoxy composites with different fiber volume contents (20%, 30%, 40%, and 50%). The effect of fiber volume contents on the tensile properties of the metallic glass fiber reinforced epoxy composites was studied by experiment and the finite element analysis method. The experiment and simulation results are in good agreement. The tensile strength and plasticity of the metallic glass fiber reinforced epoxy composites increase with the increase of fiber volume contents. When the fiber volume content is 40% or 50%, a sharply necking feature appeared on the fibers and exhibited improved plasticity, due to the formation of interacting and arresting events of shear bands occurring at the interface between the metallic glass fibers and the epoxy. In addition, the strain hardening due to plastic deformation of the metallic glass fibers further enhanced the tensile strength of the metallic glass fiber reinforced epoxy composites. This is a first step toward toughening the inherently brittle metallic glass fibers under tensile conditions.Highlights A novel CoFeSiB metallic glass fiber reinforced epoxy resin composite The increase of fiber volume fraction improves the tensile strength and plasticity of fiber reinforced composites. The strain hardening due to plastic deformation of the metallic glass fibers further enhanced the tensile strength of the metallic glass fiber reinforced epoxy composites.

The Influence of Milling Granulation on The Proportion of Fermentable and Non-Fermentable Ingredients in Mash Obtained from Mixed Endosperm Wheat

The use of purpose-selected wheat in brewing is limited because it is either not suitable for the application of usual agrotechnical measures or, more often, is not adapted to specific climatic conditions. As unmalted wheat in brewing can cause process problems and problems with the quality composition of mash/wort and consequently beer, by using the appropriate type and variety, but also by adjusting the malting process, these problems can be completely avoided or significantly reduced at the start. Two varieties were selected for the research, which in previous research showed good brewing/malting properties and which have significantly different starting values for the share of total protein (TP) in the grain. The goal of this research was to determine the effect of grain milling granulation on the quality of mash obtained from a hard type of wheat, i.e., the changes in the fermentable and non-fermentable extract ratio during mashing. Varieties with higher and lower initial contents of total protein (TP) in the grain were tested. It was found that regardless of the initial difference in TP concentration, the concentrations of total soluble proteins (TSP) and high molecular protein fraction (HMW N) are similar for varieties with higher and lower initial TP and that the difference in initial TP concentrations is shown as a difference in the concentration of insoluble protein fractions, which are eliminated during fermentation. By increasing the milling granulation in both kinds of wheat, there is a significant increase in the medium molecular protein fraction (MMW N), which is more pronounced in wheat with a lower starting concentration of TP, even though the starting concentrations of TSP in fine (Ø 0.2 mm) and the superfine milling (Ø < 0.2 mm) were similar. A significant drop in fermentability at the superfine granulation of the grain was noted.

Characteristics and Source Analysis of Volatile Organic Compounds in Typical Ozone Pollution Processes During Summer in Jinan, China

Based on a typical ozone （O3） pollution process in Jinan City from June 16 to 26, 2021, the variation characteristics of O3 and its precursor volatile organic compounds （VOCs） during different pollution periods （clean period （CP）, pollution rise period （PRP）, heavy pollution period （HPP）, and pollution decline period （PDP）） in the urban area were analyzed. Both positive matrix factorization （PMF） and an observation-based model （OBM） were used to identify the main sources of VOCs, O3 production mechanisms, and sensitive species. The results showed that the average value of ρ（O3-8h） during the HPP period in the urban area was （246.67±11.24） μg·m-3, and ρ（O3-1h） had a peak value of 300 μg·m-3. The volume fractions of VOCs and NO2 concentration were affected by the decrease in planetary boundary layer and wind speed, which were 76.99%-145.36% and 127.78%-141.18% higher than those in the other three periods, respectively, and were the main reasons for the aggravation of O3 pollution. Alkanes, oxygenated volatile organic compounds （OVOCs）, and halogenated hydrocarbons accounted for 43.81%, 20.98%, and 17.43% of VOCs in urban areas, respectively. All of them showed significant growth during the HPP period, with acetone, propane, and ethane being the top three species by volume in each stage and isopentane showing the highest growth during the HPP period. Alkene, alkanes, and aromatic hydrocarbons accounted for 40.19%, 28.06%, and 21.92% of the ozone generation potential （OFP）. 1-butene, toluene, isopentane, and isoprene were the species with higher OFP. Isoprene had the highest OFP during the PRP phase, and 1-butene had the highest OFP during the HPP phase. The volume fraction of isopentane significantly increased OFP. The correlation coefficient between VOCs and CO preliminarily indicated that motor vehicle exhaust and oil and gas volatilization were the main sources of VOCs during the HPP period. Further use of PMF revealed that solvent use sources, combustion sources, motor vehicle exhaust+oil and gas volatilization sources, industrial emission sources, and plant sources were important sources of VOCs in urban areas. The contribution of motor vehicle exhaust+oil and gas volatilization sources in the HPP period to VOCs was 3.09-14.72 times higher than that in other periods. The contribution of solvent use sources to VOCs was approximately 2.50 times higher than that in the CP and PRP periods. The main sources of VOCs volume fraction increase were motor vehicle exhaust, oil and gas volatilization sources, and solvent use sources. Potential sources and concentration weight analysis found that VOCs were also affected by the transmission of VOCs to Binzhou and Dongying in the northeast direction. The OBM results indicated that the main pathway of O3 formation in urban areas was the reaction of peroxide hydroxyl radicals （HO2·） and methyl peroxide radicals （CH3O2·） with NO, and the net ozone generation rate during the HPP phase [P（O3）net] was 24×10-9 h-1. Based on the sensitivity experiment results, the alkene components of 1-butene, propylene, cis-2-butene, and ethylene were the dominant species for O3 production.

Fluorescence Lifetime Measurement For Studying Evaporation Of Bi-Component Droplet

Sprays are essential in engineering applications like evaporators and combustion chambers. Predicting the evaporation of multi-component liquid droplets is complex due to changing composition and properties. Measuring droplet composition is challenging, with limited non-intrusive methods available. Raman spectroscopy faces hurdles like weak signals and interference. Intensity based Laser-Induced Fluorescence (LIF) requires optical models to interpret data due to varying droplet size and position. Fluorescent dyes in liquid mixtures are sensitive to temperature, complicating measurements. Fluorescence lifetime measurements offer a promising alternative, being an absolute quantity less affected by reabsorption. This study develops a novel method using fluorescence lifetime to analyze droplet composition, leveraging Time-Correlated Single Photon Counting (TCSPC) for precise measurements. Factors such as dye concentration, solvent polarity, and temperature sensitivity are investigated. Calibration curves for ethanol-water mixtures correlate fluorescence lifetime with volume fraction. Experimental setups use TCSPC and femtosecond lasers for dye excitation. Results show that fluorescence lifetime decreases linearly with solvent polarity and is influenced by temperature and dye concentration. High dye concentrations cause self-quenching, altering temperature sensitivity. The method was applied to study the evaporation of ethanol-water droplets under acoustic levitation. Findings indicate that evaporation rates slow as the water fraction increases, with initial measurements showing higher water content due to partial evaporation. This research introduces a novel technique for droplet compositional analysis using fluorescence lifetime, providing insights into optimizing measurement accuracy and advancing understanding in engineering and related fields.

Physicochemical properties of binary mixtures of cation-fluorinated ionic liquids with their non-fluorinated analogues

This work reports an investigation of the physicochemical properties (density, viscosity, refractive index and thermal stability) of four binary mixtures having a common acetate ([OAc]¯), trifluoromethanesulfonate ([OTf]¯) or bis(trifluoromethylsulfonyl)imide ([NTf2]¯) anion with either cation-fluorinated and non-fluorinated methylimidazolium (MIm) or pyridinium (Py) cations respectively, at various temperatures. The mixing behaviour of the binary mixtures was analysed by 1H and 19F Nuclear magnetic resonance (NMR) spectrometry, and the excess properties of the mixtures were calculated from the physicochemical data. The binary mixtures of fluorinated ionic liquids (FILs) with their non-fluorinated or alkyl-substituted analogues (AILs) showed an increase in density and viscosity but a decrease in refractive index with an increase in mole fraction of the pure FILs. The thermal stability of the AILs was higher than the FILs, however, an increase in the mole fraction of the pure FILs in the binary mixtures made a negligible impact on the thermal stability of the binary mixtures. These binary mixtures were found to deviate from ideal behaviour for the different physicochemical properties tending to vary between the extremes of the pure components. The large differences in properties of FILs compared with their non-fluorinated analogues were shown to be associated with the size of the fluorine atoms in the fluoro-alkyl chain, the tendency of the fluoro-alkyl chain to form aggregates with fluorinated anions, and the hydrogen bond acceptor strength of the anions. The excess properties were fitted to the Redlich-Kister polynomial equation, and no significant deviation was obtained. This study shows that the physicochemical properties of the fluorinated ionic liquids can conveniently be adjusted for specific applications by simply varying the amount of the cation-fluorinated component in binary mixtures.

Systematic experimental and model-based evaluation of the synergistic effects of alloy composition and damage rate on the formation of Cr-rich precipitates in Fe–Cr–Al alloys under ion irradiation

Fourteen Fe–Cr–Al alloys with systematically varied Cr and Al compositions were irradiated at 350∘C to 0.24 dpa by 10.5 MeV self-ions as model alloys for the Fe–Cr–Al (oxide dispersion strengthened: ODS) alloys being developed as accident tolerant fuel (ATF) cladding for light water reactors. Three dose rates (8×10−6, 8×10−5, and 8×10−4 dpa/s) were selected to predict the formation behavior of Cr-rich precipitates (CrRP) under neutron irradiation conditions. The effects of Cr, Al composition, and dose rate on the CrRP formation behavior were evaluated using a three-dimensional atom probe (3DAP) analysis. The results showed that the CrRP number density, volume fraction, and Cr concentration increase with increasing Cr composition, decreasing Al composition, and decreasing dose rate. Multiple regression analysis showed that in addition to these primary effects, there was an interaction between them on the CrRP volume fraction: (1) the higher the Al composition, the smaller the increase in the CrRP volume fraction with increasing Cr composition, and (2) the lower the Cr composition, the smaller the increase in the CrRP volume fraction with the decreasing Al composition and dose rate. It was also highlighted that to understand the dose rate effect on the CrRP formation behavior under neutron irradiation, it is useful to examine the irradiation time dependence, including the effective use of thermal aging data as a limit to the zero dose rate, in addition to the dose-dependency perspective. In addition to the systematic database of CrRP-related quantities established in this study, these considerations should contribute to further developing and validating numerical prediction models.

Cardiac Magnetic Resonance Feature Tracking Analysis for Change in Right Ventricular Function After Cardioplegic Arrest

Using echocardiography to assess right ventricular (RV) function after cardioplegic arrest is challenging. Cardiac magnetic resonance (CMR) imaging is a superior alternative, with the feature tracking technique enabling quantitative assessment of myocardial deformation. This single-center, prospective study from 2020 to 2022 assessed RV function in 42 patients who underwent open heart surgery with cardioplegic arrest. CMR data were collected preoperatively, one week postoperatively, and at follow-up (6-12 months after surgery), and assessed using the CMR feature tracking technique. Postoperatively, there was no significant change in RV end-diastolic volume, but RV end-systolic volume significantly decreased, leading to a notable increase in RV ejection fraction. By follow-up, both RV end-diastolic and end-systolic volumes had significantly reduced compared with the preoperative values. Right ventricular longitudinal contractility decreased after surgery but recovered to the preoperative values by follow-up, while RV circumferential contractility improved postoperatively and remained superior to the preoperative levels at follow-up. On CMR imaging, significant changes in RV systolic motion were observed after cardioplegic arrest, with decreased longitudinal but increased circumferential contractility. At follow up, these changes had reverted to the preoperative patterns by the mid-term (6-12 months).

Experimental study on the ignition delay characteristics of pyrolysis gas from kerosene with hydrogen peroxide addition

The ignition issue of the hypersonic aircraft remains a challenging task due to the extremely short residual time of milliseconds. To study the potential candidate of hydrogen peroxide for ignition enhancement, the ignition delay times of pyrolysis gas with the addition of 0–5000 ppm hydrogen peroxide were experimentally measured and quantitatively analyzed at temperatures of 833.8–962.1 K, equivalence ratios of 0.5–1.5, pressures of 31.9–48.8 bar, and the dilution of 45 vol% Ar. A novel injection system based on a Laval nozzle was designed to well atomize and evaporate the liquid hydrogen peroxide. The experimental results showed that the enhancing effect of hydrogen peroxide was proceeded by three stages, in which the decreasing efficiency gradually weakened with the increase of additive fraction. The ignition delay times of pyrolysis gas dramatically shortened by 66.1 % with 1000 ppm of hydrogen peroxide. Only a decrement of 19.1 % was obtained as the additive fraction increased from 1000 to 4000 ppm. The decline at 4000–5000 ppm even reduced to 2.0 %. It is suggested to add no more than 1000 ppm of hydrogen peroxide from the perspective of the highest acceleration efficiency on the ignition delay times of pyrolysis gas.

Study of celecoxib dissolution process in the mixtures of ethanol and propylene glycol at different temperatures

ABSTRACT Categorised as a nonsteroidal anti-inflammatory drug targeting the COX-2 enzyme over COX-1, celecoxib (CXB) demonstrates high membrane permeability and low aqueous solubility, placing it in class II of the biopharmaceutical classification system. Therefore, comprehension of its solubility behaviour under different configurations is desirable. The current study explores CXB solubility in propylene glycol and ethanol binary mixtures by varying temperature and cosolvent concentration, using the shake-flask method followed by spectroscopy analysis. The results show increased solubility of CXB in this mixture as ethanol mass fraction and temperature increase. Several cosolvency models were used to correlate data, including van't Hoff, Jouyban-Acree, Jouyban-Acree-van't Hoff, and mixture response surface/modified Wilson models. The mathematical models’ accuracy was investigated through mean relative deviation. The Gibbs and van't Hoff equations were employed to establish the thermodynamic features of CXB dissolution.

Yielding behaviour of chemically treated Pseudomonas fluorescens biofilms

The mechanics of biofilms are intrinsically shaped by their physicochemical environment. By understanding the influence of the extracellular matrix composition, pH and elevated levels of cationic species on the biofilm rheology, novel living materials with tuned properties can be formulated. In this study, we examine the role of a chaotropic agent (urea), two divalent cations and distilled deionized water on the nonlinear viscoelasticity of a model biofilm Pseudomonas fluorescens. The structural breakdown of each biofilm is quantified using tools of non-linear rheology. Our findings reveal that urea induced a softening response, and displayed strain overshoots comparable to distilled deionized water, without altering the microstructural packing fraction and macroscale morphology. The absorption of divalent ferrous and calcium cations into the biofilm matrix resulted in stiffening and a reduction in normalized elastic energy dissipation, accompanied by macroscale morphological wrinkling and moderate increases in the packing fraction. Notably, ferrous ions induced a predominance of rate dependent yielding, whereas the calcium ions resulted in equal contribution from both rate and strain dependent yielding and structural breakdown of the biofilms. Together, these results indicate that strain rate increasingly becomes an important factor controlling biofilm fluidity with cation-induced biofilm stiffening. The finding can help inform effective biofilm removal protocols and in development of bio-inks for additive manufacturing of biofilm derived materials.

Viscoelastic Fluid Flow Model for Hydrodynamic Behaviour of Magnetorheological Fluid in Valve and Shear Modes for a Damper System

In this present study, the flow behaviour of magnetorheological fluid in valve and shear modes for damping system is modelled and analysed. The fluid is modelled as viscoelastic fluid flowing between two parallel plates in pressure driven flow mode, and also as direct shear mode. In the work, the post-yield shear thinning or thickening behaviour of magnetorheological fluids are accounted for. The velocity and pressure distributions in the unsteady magnetorheological fluid flow between the electrodes of the damper are obtained by solving the momentum equation of the magnetorheological fluid flow using the Laplace transform method. There is an excellent agreement between the results of the present model and the results of the experimental studies. The adopted viscoelastic flow model describes that the rheological behaviour of the fluid is separated into distinct pre-yield and post-yield regimes. The fluid flow velocity, velocity gradient, and shear stresses have all been shown to be enhanced by an increase in the pressure drop. The viscosity of the fluid increases with an increase in the volume fraction of particles in the fluid, which causes the resistance of the fluid to flow to increase and thereby, reduces the fluid flow velocity. Fluid flow velocity is decreased as a result of increasing magnetic field strength. The design of clutches, rotary brakes, dampers, shock absorbers, prosthetic devices, polishing and grinding tools, etc. will all benefit greatly from the adoption of the current model.

Early On-Treatment Assessment of T Cells, Cytokines, and Tumor DNA with Adaptively Dosed Nivolumab + Ipilimumab: Final Results from the Phase 2 ADAPT-IT Study.

The Adaptively Dosed ImmunoTherapy Trial (ADAPT-IT;NCT03122522) investigated adaptive ipilimumab discontinuation in melanoma based on early radiographic assessment. Initial findings indicated similar effectiveness compared with conventional nivolumab-ipilimumab (nivo-ipi). Exploratory biomarker analyses and final clinical results are now reported. Patients with unresectable melanoma received two doses of nivo-ipi. Radiographic assessment at Week 6 informed continuation of ipilimumab before nivolumab maintenance. The primary endpoint was overall response rate at Week 12. Plasma was assayed for circulating tumor DNA and 10 cytokines using a multiplex immunoassay. Flow cytometry of peripheral blood mononuclear cells was performed with an 11-color panel. Among the treated patients, expansion of proliferating T-cell populations was observed in responders and nonresponders. Baseline IL6 levels were low in patients achieving an objective radiographic response (median 1.30 vs. 2.86 pg/mL; P = 0.025). High baseline IL6 levels were associated with short progression-free survival [PFS; HR = 1.24, 95% confidence interval (CI), 1.01-1.52; P = 0.041]. At Week 6, patients with response had lower average tumor variant allele fractions than nonresponders (median 0.000 vs. 0.019; P = 0.014). Greater increases in average variant allele fractions from baseline to Week 6 correlated with short PFS (HR = 1.11, 95% CI, 1.01-1.21; P = 0.023). Week 12 overall response rate was 47% (95% CI, 35%-59%) with a median follow-up of 34 months among survivors. Median PFS was 21 months (95% CI, 10-not reached); 76% of responses (95% CI, 64%-91%) persisted at 36 months. Adaptively dosed nivo-ipi responses are durable and resemble historical data for conventional nivo-ipi. Baseline IL6 and circulating tumor DNA changes during treatment warrant further study as biomarkers of nivo-ipi response.

Designing Plastrons for Underwater Bubble Capture: From Model Microstructures to Stochastic Nanostructures.

Bubbles and foams are often removed via chemical defoamers and/or mechanical agitation. Designing surfaces that promote chemical-free and energy-passive bubble capture is desirable for numerous industrial processes, including mineral flotation, wastewater treatment, and electrolysis. When immersed, super-liquid-repellent surfaces form plastrons, which are textured solid topographies with interconnected gas domains. Plastrons exhibit the remarkable ability of capturing bubbles through coalescence. However, the two-step mechanics of plastron-induced bubble coalescence, namely, rupture (initiation and location) and subsequent absorption (propagation and drainage) are not well understood. Here, the influence of 1) topographical feature size and 2) gas fraction on bubble capture dynamics is investigated. Smaller feature sizes accelerate rupture while larger gas fractions markedly improve absorption. Rupture is initiated solely on solid domains and is more probable near the edges of solid features. Yet, rupture time becomes longer as solid fraction increases. This counterintuitive behavior represents unexpected complexities. Upon rupture, the bubble's moving liquid-solid contact line influences its absorption rate and equilibrium state. These findings show the importance of rationally minimizing surface feature sizes and contact line interactions for rapid bubble rupture and absorption. This work provides key design principles for plastron-induced bubble coalescence, inspiring future development of industrially-relevant surfaces for underwater bubble capture.

Solid-Liquid Phase Equilibria of the Pb2+, Ca2+, Mg2+//Cl--H2O Quaternary System and Its Subsystems at 303.2 K.

The solid-liquid phase equilibria of the ternary systems Pb2+, Ca2+//Cl--H2O, Pb2+, Mg2+//Cl--H2O, and Ca2+, Mg2+//Cl--H2O were investigated at atmospheric pressure and T = 303.2 K using the isothermal dissolution equilibrium method. Additionally, solid phase equilibria of the quaternary system Pb2+, Mg2+, and Ca2+//Cl--H2O were determined, and the corresponding stable phase diagrams and density-composition diagrams were constructed. The results indicate that the phase diagrams of Pb2+, Ca2+//Cl--H2O mainly consist of a ternary invariant point, two solubility curves, and four crystalline regions, while there are two ternary invariant points, three solubility curves, and six crystalline regions in the Pb2+, Mg2+//Cl--H2O and Ca2+, Mg2+//Cl--H2O systems. The results of the density-versus-w(CaCl2) plots of the various ternary systems confirm that the density of the equilibrium solution tends to go upward with the increase in the mass fraction of CaCl2. The density of various ternary systems reaches the maximum and equilibrium at the corresponding invariant point, and there is no significant change with the further increase in the CaCl2 mass fraction. Furthermore, the phase diagram of the Pb2+, Mg2+, Ca2+//Cl--H2O quaternary system includes two invariant points, five isothermal dissolution curves, and five crystalline regions. The order of the relative areas of the crystalline regions for the five salts is PbCl2 > CaCl2·2MgCl2·12H2O > 2PbCl2·3MgCl2·18H2O > MgCl2·6H2O > CaCl2·4H2O.

Evaluating mechanical and biological responses of bipolymeric drug-chitosan-hydroxyapatite scaffold for wounds: Fabrication, characterization, and finite element analysis

This study aims to explore the potential of a scaffold composed of drug-chitosan-hydroxyapatite (HA) in improving tissue treatment. The focus of the investigation lies in analyzing the physical and biological properties of the scaffold and evaluating its mechanical characteristics through finite-element analysis. To synthesize microcapsules containing dextran-diclofenac sodium, the electrospraying method was employed. The drug-chitosan-HA scaffold with varying volume fractions (VF) of the synthesized microcapsules (10, 15, and 20) was fabricated using the freeze-drying technique. Microscopic and scanning electron microscopy (SEM) images were utilized to evaluate the morphology, shape, and size of the microcapsules, as well as the porosity of the scaffolds for wound healing purposes. The mechanical properties of the synthesized microcapsules were determined via a nanoindentation test, while the mechanical behavior of the fabricated scaffolds was assessed through compression testing. Additionally, a multiscale finite-element model was developed to predict the mechanical properties of tissue scaffolds containing pharmaceutical microcapsules. The findings indicate that the incorporation of drug-chitosan-hydroxyapatite into the tissue significantly enhances both mechanical and biological responses. The mechanical evaluations demonstrate that the drug-chitosan-hydroxyapatite tissue exhibits excellent resistance to pressure, making it a suitable protective covering for skin wounds. Moreover, biological evaluations reveal that an increase in scaffold porosity leads to higher swelling behavior. The scaffold containing 20 % pharmaceutical microcapsules demonstrated the greatest swelling and desirable antibacterial properties, thereby indicating its potential as an effective wound dressing. Furthermore, a multiscale finite-element model was developed to predict the mechanical properties of tissue containing pharmaceutical microcapsules. The results indicated that the average size of the microcapsules was in the range of 170 to 180 µm, and the porosity of the prepared tissue was between 52 % and 61 %. The experimental compressive properties revealed that an increase in the volume fraction of the embedded microcapsules led to an increase in the maximum compressive stress and compressive modulus of the scaffolds by up to 54.95 % and 53.18 %, respectively, for the scaffold containing 20 % VF of pharmaceutical microcapsules compared to the specimen containing 10 % VF. In conclusion, the developed scaffold has the potential to serve as an effective wound dressing, with the ability to provide structural support, facilitate controlled drug release, and promote wound healing.

Anti-temperature anti-salinity anti-shear C18MAAC / NaAA Amphiphilic Copolymer: Preparation, characterization and properties

For improving the temperature resistance, salt resistance and shear resistance of conventional copolymers, the new hydrophobic monomer C18MAAC was prepared by substitution, then C18MAAC/NaAA amphiphilic dicopolymer was prepared by micellar polymerization. The synthetic parameters were optimized using the single-variable method: reaction temperature 50°C, mass fraction of initiators to the total monomers 0.7 wt%, mass fraction of hydrophobic monomer C18MAAC to NaAA and C18MAAC 2 wt%, and the mass fraction of two monomers 25 wt%. The structure of the C18MAAC and the C18MAAC/NaAA copolymer were characterized, and the morphology of the copolymer was observed. Effect of mass fraction of the copolymer and the salt, temperature, shear rate on viscosity of the aqueous solution were investigated. With the increase of copolymer's mass fraction, the viscosity of the aqueous solution increased slowly first, and the viscosity increases rapidly after reaching 0.4 wt% of copolymer concentration. Therefore, 0.5 wt% concentration of copolymer aqueous solution was selected in the experiment, and the rotor was selected for the rheological performance test. The results showed that the temperature resistance, salt resistance and shear resistance of the copolymer reached 90 °C, 1 wt% salt and 150 s-1 respectively. The C18MAAC/NaAA copolymer/surfactant composite system is very stable in 1wt% salt at 90 °C, and has good synergistic effect to improve the viscosity of the solution, which making it is a promising candidate as an oil-displacing agent.

Dynamic and phase transition studies of ionic surfactant-stabilized oil/water microemulsion: Effects of volume fraction, polymer grafting, and temperature

In this work, we study the dynamic/phase transition relationship of a system composed of spherical particles of oil/water microemulsion, stabilised by an ionic surfactant based on cetylpyridinium chloride (CpCl) and an octanol-based cosurfactant, and dispersed in salt water. We examine a large range of volume fractions Φ. To do this, we use molecular dynamics simulations with an appropriate interaction potential that accounts for Van der Waals and electrostatic interactions. We also graft different numbers of dodecyl-(polyethylene oxide)227-dodecyltriblock copolymers onto the microemulsion nanodroplets, which we denote (n(D−PEO227−D)), where n varies from 0 to 12. Specifically, we treat the dynamic properties, using the mean square displacement (MSD) and diffusion coefficients, and then use Arrhenius law to determine the activation energy. In our study, we vary three main parameters: the volume fraction, the number of polymer added to the n(D−PEO227−D) microemulsion, and the temperature. The result shows a transition from the sol to the gel state of the bare microemulsion as the volume fraction increases or as the temperature decreases. Also, it proves that when a D-PEO-D polymer is added to the microemulsion, the system rapidly changes its state either as the volume fraction Φ increases or as the temperature T decreases. We also calculate the activation energy of the bare particles in the microemulsion at different volume fractions (ϕ) using the Arrhenius equation.

Research on particle migration in fractures driven by gas-liquid two-phase flow during deep energy storage and extraction

Particle-laden fluid flow in fracture encompasses various deep geo-energy projects, including but not limited to hydraulic fracturing, mud and water inrush, and sand production. The migration of particles under fluid flow seriously affects the stability of geo-energy engineering and understanding the mechanisms is of great importance. This study presents a numerical investigation of particle-laden fluid flow in rock fractures under two-phase flow. A coupled approach of resolved computational fluid dynamics (CFD) and discrete element method (DEM) is employed to capture the particle movements and variations in hydraulic properties, with the volume of fluid (VOF) method to reproduce the two-phase flow. The results indicate that the model with gas injection exhibits higher particles migration velocity compared to that without gas due to the increase in fluid velocity and fluctuation in drag force. Particles migration velocity presents an initial increase followed by a subsequent decrease as the gas fraction increases, which can be attributed to the initial rise followed by a subsequent decline in the drag force. In addition, the sensitive analysis shows that the particle migration velocity decreases with the increase of liquid viscosity and fracture roughness in the fluid, and further accelerates with the increase of particle size and hydraulic gradient. Our results have important implications for understanding the mechanisms of particle migration in rock fractures driven by the multiphase flow during deep energy storage and extraction.

The Stability of a Tumor–Macrophages Model with Caputo Fractional Operator

This study proposes a fractional-order model in the Caputo sense to describe the interaction between tumor and immune macrophages by assuming that the pro-tumor macrophages induce a Holling type-II response to the tumor. Then, the basic properties of the solutions to the model are studied. Local stability analysis is conducted at each of the equilibria in the model, and a numerical study is performed with varying activation rates of type-II or pro-tumor macrophages and the order of the fractional operator. The numerical findings suggest that type-I or anti-tumor macrophages can stabilize the system if the activation rate of type-II or pro-tumor macrophages is low. Still, for a higher value of the activation rate for type-II or pro-tumor macrophages, the proliferation of tumor cells is uncontrollable and the system becomes unstable. Furthermore, the stability of the system decreases as the order of the fractional operator increases.

Heat transfer in radiative hybrid nanofluids over moving sheet with porous media and slip conditions: Numerical analysis of variable viscosity and thermal conductivity

Our current numerical investigation aims to estimate the thermal transport properties of hybrid nanofluids on a moving surface that is being shrinked horizontally. The hybrid nanoparticles consist of alumina (Al2O3) and copper (Cu), suspended in water as the base fluid. The transportation phenomenon takes place in a Darcy-Forchheimer medium, which is a porous material that exhibits thermal radiation, variable viscosity, variable thermal conductivity, Joule heating, viscous dissipation, and the effects of velocity and thermal slip conditions. The governing partial differential equations (PDEs) are converted using suitable similarity transformations into non-linear ordinary differential equations (ODEs). The equations were solved using the shooting technique with the RK-IV algorithm in the MATHEMATICA program. Dimensionless velocity, temperature, skin friction, and Nusselt numbers all provide numerical outcomes. Graphs and tables show the results of an investigation into the influence of different physical characteristics on these numbers. The velocity profile exhibits an upward trend when the velocity slip and nanoparticles volume fraction rise, but a downward trend when the viscosity and Prandtl number are varied. if the thermal slip and variable Prandtl number grow, the temperature profile falls. Conversely, if the nanoparticles volume fraction and variable thermal conductivity increase, the temperature profile increases. The skin friction and Nusselt number exhibit an upward trend as the volume percentage of nanoparticles and the viscosity of the system rise. At a Prandtl number of 6.2 and a nanoparticle volume fraction of 1 %, the Xue model demonstrates a heat transfer rate increase that is 5.32 % superior to the Yamada-Ota model and 3.18 % superior to the Hamilton-Crosser model for nanofluid. In the case of hybrid nanofluid, the Xue model exhibits a 19.01 % superiority over the Yamada-Ota model and 12.197 % superior to the Hamilton-Crosser model.