Viscosity Reduction Research Articles

Simulation of supersonic axisymmetric base flow with a data-driven turbulence model

Axisymmetric base flow involves massive flow separation which is challenging for a typical Reynolds-averaged Navier-Stokes (RANS) turbulence model. Furthermore, a supersonic condition imposes additional difficulties to a turbulence model in predicting strong compressibility effects associated with the flow separation phenomena. A data-driven approach is pursued here to improve a turbulence model. The Spalart-Allmaras model is corrected from an optimization process, and then the model correction is mapped to local flow features through a machine learning process. For the optimization-combined machine learning method, the field inversion and machine learning framework is adapted here with three major modifications. First, a zonal-field inversion method is suggested to avoid the undesired modification of attached flow in the optimization process for the model correction. Second, the RANS model is modified by adjusting a net balance between the production and destruction terms in the RANS equation. Third, the local Mach number is included in the machine learning process to incorporate compressibility effects of the supersonic flow. The current study indicates that the improved RANS model reduces the eddy viscosity in the separated region, compared to the baseline RANS model. The reduction of the eddy viscosity helps to predict the base expansion of the supersonic flow and the size of the recirculation region. Current computations are compared with relevant literature data including wake velocity profiles and the base pressure in the wide range of the supersonic Mach number.

Enhancing flame retardancy and hydrolysis resistance of flame retardant copolyester fibers by reactive carbodiimide

Polyethylene terephthalate flame retardant copolyester (FRPET) copolymerized with 2-carboxyethyl (phenyl) phosphinic acid (CEPPA) is one of the major copolymerized commercial flame-retardant copolyesters. Similar to conventional PET fibers, the mechanical and flame retardant properties of FRPET fibers after alkaline water post-treatment are reduced. In this work, two kinds of carbodiimide-based masterbatches are added to FRPET fibers, the thermal processing stability, hydrolysis resistance and flame retardancy are significantly improved. The structural and physicochemical properties of the modified FRPET fibers were characterized. The processing thermal stability of FRPET is improved due to the reaction of the double bond structure in carbodiimide with the terminal carboxyl group of polyester to form an acyl urea structure. After melt extrusion, the viscosity reduction of the modified FRPET fiber is only 1.6 %, which is about 10 times lower compared to that of FRPET (17.6 %). After being treated with 50 g/L NaOH solution at 95 °C for 1 h, the tensile strength retention rates of the modified FRPET fibers are over 85.0 %, which is much higher than that of FRPET fibers (71.8 %), showing excellent hydrolysis resistance. In addition, the vertical burning performance of the modified FRPET fibers is improved from V-2 to V-0, and the limiting oxygen index could still reach 25.6 %. Besides that, the mechanism of the combustion process is further discussed.

Adaptable intelligent filters based on nanotextured nonwoven membranes containing water-insoluble hydrogels

The work demonstrates, for the first time, thermo-responsive, water-insoluble, hydrogel-based, nano-fibrous filter media comprised of copolymers of N-isopropylacrylamide (NIPAM) and methyl methacrylate formed by electrospinning. Moreover, a comprehensive novel physical explanation of all aspects responsible for the physical mechanisms resulting in the thermo-responsive regulation of the water flow rate and an enhanced interception of nanoparticles by such filter membranes is given. They are the wettable-non-wettable transition, pore, and fiber-size changes, as well as a diminishing filter thickness at the lower critical solution temperature (LCST) of the copolymers developed here, which interplay with a significant reduction in the water viscosity with temperature. Poly(N-isopropylacrylamide) (PNIPAM) hydrogel is an attractive material because of its thermo-responsive properties. Its wettability changes with water temperature. This characteristic holds great promise for the development of advanced filter media and related responsive materials. In this study, PNIPAM hydrogels were designed and transformed into filter membranes for applications in water filtration in biomedical and other related systems. These thermo-responsive filter membranes offer the potential for enhanced filtration efficiency, selectivity, and the overall system performance. Here, two different procedures were adopted to form water-insoluble thermo-responsive filter media based on PNIPAM hydrogels. The PNIPAM-based hydrogels were electrospun, resulting in the formation of thermo-responsive water-insoluble nanofiber membranes. These membranes underwent a series of comprehensive experiments to assess their performance and characteristics, including mass loss, water droplets for the wettability assessment, filtration tests, shrinkage measurements, and microscopic observations. These diverse experiments yield a full understanding of the PNIPAM-based nanofiber membranes’ properties and their potential applications.

A Novel Prediction Model for Steam Temperature Field of Downhole Multi-Thermal Fluid Generator

Aiming at the low efficiency of heavy-oil thermal recovery, a downhole multi-thermal fluid generator (DMTFG) can improve the viscosity reduction effect by reducing the heat loss of multi-thermal fluid in the process of wellbore transportation. The steam generated by the MDTFG causes damage to the packer and casing, owing to the return upwards along the annular space passage of the oil casing. To mitigate this damage, a heat transfer model for multi-channel coiled tubing wells and a prediction model for the upward return of the steam temperature field in the annulus were established with the basic laws of thermodynamics. Models were further verified by ANSYS. The results indicate the following four conclusions. First of all, when the surface pressure is constant, the deeper the located DMTFG, the shorter the distance for the steam to return would be. It is easier to liquefy the steam. Second, the higher the temperature of the steam produced by the downhole polythermal fluid generator, the larger the upward distance of the steam would be. Third, the higher the steam pressure at the outlet of the downhole polythermal fluid generator, the smaller the distance of steam upward return would be. Finally, the larger the diameter of the multi-channel conversion piping, the greater the distance of the steam return would be. It is meaningful to provide valuable theoretical guidance for packer position designing in the field. Meanwhile, the study also provides a modeling basis for the subsequent study of artificial intelligence in the downhole temperature field.

Synthesis of terpolymer from Helianthus annuus (natural oil) and evaluation as pour point depressant and viscosity reducer on Indian crude oil

Pour Point Depressant is introduced to crude oil at ppm level to overcome transportation problem of crude oil because of its complex chemical structure. Synthesized PPDs improve flow property, viscosity and also improve its numerous parameters to improve performance of crude oil. Low molecular weight and high molecular weight, copolymer having better PPD types. In present work, synthesized Terpolymer, from natural source, was formed from the reaction with Helianthus annuus oil and ester of Erucic Acid with various fatty alcohol. It was evaluated for its properties on Indian waxy crude oils, i.e., From Limbodra well. Structure and molecular weight of synthesized polymer was confirmed by Spectral data and Gel permeation chromatography (GPC). Also its effect on crude oil was evaluated by Rheological studies, SARA Analysis, Pour point depressant effect. Cross–polarizing microscopic studies were performed to study changes in morphology of wax crystals in crude oil with and without additive. A zero friction advanced Rheometer AR-500 was used to determine the viscosity by applying Bingham plastic-flow model.

Experimental and theoretical insight into the effect of a novel composite dispersant on the properties of coal pitch water slurry

To optimize the utilization efficiency of coal pitch (CP), an innovative composite dispersant was designed and employed in the preparation of coal pitch water slurry (CPWS) by effectively combining modified sodium lignosulfonate (MLS) and amphoteric polycarboxylate (AAD) based on the principle of complementary advantages. The effects of the proportion of MLS to AAD on the characteristics of CPWS were systematically analyzed and assessed by various technical methods, including apparent viscosity, rheological behavior, static stability, adsorption behavior, etc. Results indicated that the CPWSs utilizing distinct composite dispersants belonged to the category of yield pseudoplastic fluids and had a good correlation with the Herschel-Bulkley model. Among them, the CD-2, composite dispersant with a mass ratio of MLS:AAD = 1:1, exhibited superior performance in terms of viscosity reduction and stabilization properties. It demonstrated the maximum adsorption capacity (5.23 mg/g) and adsorption layer thickness (7.22 nm) compared to other dispersants. Meanwhile, it could significantly increase the wettability (with a contact angle of 74.5°) and the absolute Zeta potential value (32.5 mV) of CP. The density functional theory (DFT), molecular dynamics (MD) simulation, and extended Derjaguin-Landua-Verwey-Overbeek (eDLVO) theory were carried out to investigate the interaction mechanism of composite dispersant with CP and the interaction energy among CP particles. The differences in energy levels between the lowest unoccupied molecular orbital (LUMO) and the highest occupied molecular orbital (HUMO) of MLS and AAD were significantly smaller than that of H2O. The hydrophobic groups of composite dispersants were efficiently adsorbed onto CP, while the hydrophilic groups adsorbed water molecules, with an adsorption energy reaching −169.36 kcal/mol. The steric hindrance of composite dispersant exerted a crucial influence on the dispersion of CPWS, enabling CP particles to be stabilized in water. The present study offers a novel approach to enhance the characteristics of CPWS and establishes a theoretical foundation for the design of efficient composite dispersants.

A new approach for grafting plasticized cellulose acetate biodegradable plastic with maleic anhydride: Processing and characterization

AbstractGrafting polymers with reactive maleic anhydride is a common approach for the synthesis of new material with the capability of acting as a compatibilizer in polymer blends. Accordingly, this research showed a new approach for grafting maleic anhydride onto renewable cellulose acetate using an initiator. The grafting process through extrusion showed good stability with continuous production of all grafted samples. Moreover, two different grafting processes, namely one‐step and two‐step processes, were shown to produce materials with very similar characteristics. Grafting of maleic anhydride onto cellulose acetate by reacting with its hydroxyl groups was confirmed by both Fourier transform infrared spectroscopy and nuclear magnetic resonance analysis. Rheological studies also demonstrated the enhanced flowability and lower viscosity of the grafted material in comparison to the plasticized cellulose acetate.Highlights Grafting maleic anhydride onto plasticized cellulose acetate by reactive extrusion. Detection of grafted maleic anhydride onto cellulose acetate through NMR analysis. High thermal stability of grafted materials. Significant reduction in viscosity of plasticized cellulose acetate after grafting

Performance of eco-friendly soy protein adhesive reinforced by aldehyde sodium alginate

Faced with many challenges such as energy crisis and environmental protection issues, biomass soy protein-based adhesives for replacing aldehyde-based adhesives have gradually become one of the research hotspots for wood industry upgrading. However, soy protein-based adhesives still have many shortcomings. Low bonding strength, poor water resistance and high viscosity restrict their widespread industrial application. In this work, a modified soy protein isolate (SPI) based adhesive with strong water-resistant bonding strength and low viscosity was prepared. Oxidized sodium alginate (OSA) and calcium ions were employed in SPI adhesive system. Results showed that cross-linking between OSA, calcium ions and SPI occurred successfully. The mechanical properties of SPI were significantly improved. The dry and wet bond strengths were 2.05 MPa and 0.97 MPa, respectively, in 65.3 % and 49.2 % increments for comparison. The adhesive samples also showed a reduction in viscosity and an increase in thermal stability. It can be developed as a facile method for preparing bio-adhesives.

Rheological and Mechanical Characterization of 3D-Printable Solid Propellant Slurry.

This study delves into the rheological and mechanical properties of a 3D-printable composite solid propellant with 80% wt solids loading. Polybutadiene is used as a binder with ammonium sulfate, which is added as an inert replacement for the ammonium perchlorate oxidizer. Further additives are introduced to allow for UV curing. An in-house illumination system made of four UV-A LEDs (385 nm) is employed to cure the resulting slurry. Rheological and mechanical tests are conducted to evaluate the viscosity, ultimate tensile strength and strain, and compression behavior. Viscosity tests are performed for both pure resin and complete propellant composition. A viscosity reduction factor is obtained for the tested formulations when pre-heating slurry. Uniaxial tensile and compression tests reveal that the mechanical properties are consistent with previous research. Results emphasize the critical role of temperature and solid loading percentage. Pre-heating resin composites may grant a proper viscosity reduction while keeping mechanical properties in the applicability range. Overall, these findings pave the way for the development of a 3D printer prototype for composite solid propellants.

Study on the Catalytic Oxidation Modification Effect of Heavy Oil at Low Temperature under the Action of Different Ligand Ferric-Based Systems

This work explores the low-temperature catalytic oxidation of heavy oil (140 °C), resulting in structural changes with reduced heavy components and increased light components. The catalytic oxidation system consists of a catalyst, an oxidant, and a proton donor. Four different complexes of iron-based catalysts were utilized: ferric oleate, iron naphthenate, EDTA–FeNa, and EDDHA–FeNa. Catalytic oxidation processes with these catalysts produced four types of oxygenated oil, which were then analyzed using group composition analysis and a viscosity test. The results show that EDDHA–FeNa is more favorable for the catalytic oxidation of heavy oil in a low-temperature environment, achieving a viscosity reduction rate of 78.57%. Furthermore, the catalytic performance of heavy oil oxidation was investigated using EDDHA–FeNa as catalyst under three conditions: the amount of catalyst, oxidant and reaction temperature. These findings may provide researchers valuable guidance and principles for the investigation and development of advanced catalytic viscosity reduction of heavy oil.

Recovery mechanisms of shale oil by CO2 injection in organic and inorganic nanopores from molecular perspective

CO2 injection is the feasible method to enhance shale oil recovery and has attracted extensive attention in recent years. Since shale reservoir has omnipresent nanoscale pores, understanding the underlying CO2-EOR mechanisms at the nanoscale is of critical importance. In this work, we study the structural and dynamic properties of CO2/nC8 systems in organic kerogen and inorganic quartz nanopores by molecular dynamic simulation and clarify the dominant EOR mechanisms of CO2 injection in various mineral nanopores. We find a large positive slip velocity occurs when single-phase nC8 flows in quartz nanopore while it is no-slip boundary condition in kerogen nanopore. The CO2-regulated nC8 in quartz nanopore is the joint effect of slip, competitive adsorption and viscosity reduction. In the first stage, CO2 extracts the first adsorption layer of nC8 by competitive adsorption and forms a CO2 film on the quartz surface. The CO2 film reduces the slip velocity between nC8 and quartz surface and weakens the nC8 flow capacity. After CO2 adsorption is saturated, the CO2 mixes with nC8 in all flow regions and the effective viscosity of nC8 starts decreasing at this stage. The flow capacity of nC8 rises dramatically due to the viscosity reduction mechanism of CO2. In kerogen nanopore, it is no-slip boundary condition and CO2 mixes with nC8 in all flow regions directly instead of preferably adsorbed on the surface. Viscosity reduction is the dominant mechanism to affect nC8 flow behavior and nC8 flow capacity is enhanced monotonically as CO2 injection. Our study advances the understanding of the recovery mechanisms of shale oil by CO2 injection on nanoscale and provides the theoretical foundation for the optimization of CO2-EOR in shale oil reservoirs.

Microcosmic mechanism of asphalt-aggregate interface adhesion failure under freeze-thaw cycles based on molecular dynamics

ABSTRACT In order to investigate the micro-mechanisms of adhesive failure at the asphalt-aggregate interface under freeze-thaw cycling, this study presents a novel model for freeze-thaw cycling of asphalt mixtures constructed using molecular dynamics. The model is employed to explore the micro-mechanisms of adhesive failure between asphalt and aggregate surfaces under freeze-thaw cycling conditions. Utilising the four-component model of asphalt, asphalt molecules were constructed, with silicon dioxide and calcium carbonate chosen to represent acidic and alkaline aggregates, respectively. Subsequently, an asphalt-aggregate-water freeze-thaw cycling model was developed. Building upon this foundation, the variations in interface interactions between asphalt and the two types of minerals were analysed under the same freeze-thaw cycling conditions but differing freeze-thaw cycle counts. This analysis was conducted through the examination of Radial Distribution Function (RDF), water molecule coordination numbers, and hydrogen bond quantities at the interfaces between asphalt and the two mineral types. The research findings indicate that acidic aggregates exhibit a greater affinity for water molecules compared to alkaline aggregates. Hydrogen bond interactions exist between aggregates and water molecules, with the hydrogen bond energy being greater than the interactions between asphalt molecules and aggregate surfaces. The cohesive energy decreases with an increasing number of freeze-thaw cycles, leading to a gradual reduction in asphalt viscosity and facilitating the detachment of asphalt from the aggregate surface. Consequently, acidic aggregates tend to absorb water molecules more readily, and water can lower the viscosity of asphalt molecules, ultimately resulting in the macroscopic delamination of asphalt from the aggregate surface. These research outcomes provide valuable theoretical guidance for a deeper exploration of the adhesive failure mechanisms in asphalt-aggregate interactions.

Multi-phase behavior and pore-scale flow in medium-high maturity continental shale reservoirs with Oil, CO2, and water

The application of CO2 to enhancing the recovery of continental shale oil has attracted considerable attention. However, the introduction of CO2 leads to intricate phase behavior and flow mechanisms. In this study, firstly, a three-phase equilibrium model is developed, with nano-confinement effects taken into consideration, to analyze the phase behavior of continental shale oil-CO2-water systems in both a bulk phase and nanopores. Building upon this, an improved pore network model is introduced to simulate steady-state oil–water flow while considering the alterations in fluid properties resulting from CO2 dissolution. The findings reveal that with the increase of CO2 injection, a transition from two phases of liquid and water to two phases of vapor and water, three phases of liquid, vapor and water, two phases of vapor and water, and ultimately a pure vapor phase occurs. The dissolution of CO2 exerts a pronounced impact on the composition and properties of the oil phase, and the viscosity and interfacial tension reduction effects play a central role in affecting the flow capacity. Nano-confinement effects facilitate the transfer of vapor-phase molecules into the water and oil phases, thus increasing the concentration of CO2 in the oil and water phases. The pore-scale flow results reveal that upon injection, water quickly traverses the larger pores. More smaller pores become accessible after CO2 dissolution, significantly boosting the extraction of shale oil from these smaller pores and slightly reducing the water output.

Co-pyrolysis of saw dust and oily sludge with waste-heat utilization of steel slag on rotary kiln simulated engineering practice

Pyrolysis of oily sludge (OS) possesses actual problems of high viscosity and high energy consumption in industry. This paper introduced saw dust (SD) to achieve physical viscosity reduction of OS, and then completed OS pyrolysis via steel slag (SS) with sufficient waste heat to replace external heat sources. The rotation of rotary kilns reactor with fins inside were utilized for pyrolysis, which exhibited excellent heat transfer effect for SS heating as validated by discrete element analysis (DEM) simulation. Temperature program and fixed temperature pyrolysis were respectively investigated and the latter one obtained higher yield of oil and gas. Especially SD addition increased the yield and quality of calorific value products (pyrolysis oil and gas). SS not only provided heat source but a lot had catalytic effect on pyrolysis, in which the [O] compounds provided by metal oxides could destroy the stability of chemical bond and deepen the cracking reaction. The energy equilibrium was calculated by heat capacity and reaction energy barrier. Finally, the pyrolytic residue was utilized as soil remediation agent by evaluating Ryegrass growth. Trace FeOx promoted photosynthesis and cellular respiration in plants, while excessive FeOx led to difficulty in respiration and decay of roots. Therefore, this new approach provides an alternative direction for collaborative treatment of OS, SD, and SS with co-benefits from three feedstocks to save energy and produce high-quality products of gas and oil.

Enhanced oil recovery by using modified ZnO nanocomposites in sandstone oil reservoirs

Recently, nanocomposites were employed to improve the extraction of oil in different reservoirs. Due to the unique characteristics of nanoparticles such as small size, efficient altering main mechanisms such as IFT, CA, and viscosity reduction, have received wide attention among researchers. This study investigated the application of a newly designed ZnO-cerium N-composite for EOR at reservoir conditions, and the performance was compared to the standalone ZnO nanoparticles. After performing the morphology of the N-composite, the effect of the N-composites on the wettability alteration, interfacial tension, viscosity, Zeta potential, pH, and density was studied at different N-composites concentrations at reservoir conditions. Based on the results of rock/fluid interactions at the static phase, an optimum concentration was chosen for performing dynamic core flooding experiments. At 100 ppm, the highest stability and the highest reduction in capillary force were observed. The presence of Ce in the structure of the N-composite changes the pore volume of ZnO-Ce compared to ZnO nanoparticles, which affects the surface charge. IFT (mN/m), CA (°), and zeta potential (mV) were (22.51, 40.83, and − 44.36), and (30.50, 50.21, and − 31.05) for ZnO-Ce and ZnO, respectively at 100 ppm. By application of the optimized nanofluid in an oil displacement study, RF in the presence of ZnO-Ce, and ZnO were 37.11% and 71.40%, respectively.

Development of Novel Silicon Quantum Dots and Their Potential in Improving the Enhanced Oil Recovery of HPAM.

Hydrolyzed polyacrylamide (HPAM) is commonly used in polymer flooding, however, it is prone to viscosity reduction at high temperatures and high salinities, weakening its ability to improve oil recovery. In this work, sulfonated modified silicon quantum dots (S-SiQDs) were synthesized and then added to HPAM to study the improvement of rheological properties and enhanced oil recovery performance of HPAM at high temperatures and salinities. It is found that the S-SiQDs with a concentration of only 0.1 wt % can significantly increase the viscosity of HPAM from 28.5 to 39.6 mPa·s at 60 °C and 10,000 mg/L NaCl. Meanwhile, the HPAM/S-SiQDs hybrid solution always possessed higher viscosity and viscoelastic moduli than HPAM, attributed to the hydrogen bonding between HPAM and S-SiQDs. Notably, HPAM/S-SiQDs still maintained elastic behavior at harsh conditions, indicating that they formed a strong network structure. Through oil displacement experiments, it was found that the oil recovery of HPAM/S-SiQDs was higher (28.3%), while that of HPAM was only 17.2%. Thereafter, the utilization sequence of oil during the displacement process was studied with nuclear magnetic resonance experiments. Ultimately, the oil displacement mechanism of HPAM/S-SiQDs was deeply analyzed, including viscosity thickening and wetting reversal.

Preparation and performance study of anti mud polycarboxylic acid slump retaining agent

Anti-mud polycarboxylic acid slump retaining agent was prepared by copolymerization of ethylene glycol monovinyl polyethylene glycol ether, diethyl 4-vinylphenyl phosphate, 2-methyl-2-(4-vinylphenyl) propionic acid, unsaturated carboxylic acid (or unsaturated carboxylic anhydride) and unsaturated carboxylic ester under the action of initiator and molecular weight regulator. The effect of the slump retaining agent on the workability of fine aggregate concrete with different mud contents was tested, and the sensitivity of the slump retaining agent to the mud content of machine-made sand was evaluated. At the same time, the viscosity reduction performance of the slump retaining agent was evaluated by using the emptying time of the inverted slump cone and the flow time of V-funnel and L-box. The experimental results show that the synthesized anti-mud polycarboxylic acid slump retaining agent has favourable effects of anti-mud and viscosity reduction.

Electroosmosis of viscoelastic fluids in pH-sensitive hydrophobic microchannels: Effect of surface charge-dependent slip length

We analytically investigated the electroosmotic flow characteristics of complex viscoelastic liquids within a charged hydrophobic microchannel, considering the pH and salt concentration-dependent surface charge effects in our analysis. We examined the variation of the electric-double layer (EDL) potential field, the surface charge-dependent slip (SCDS) length, the flow field, the viscosity ratio, and both normal and shear stresses in relation to the bulk pH, bulk salt concentration, and Deborah number of the solution. Our current findings indicate that, under strong flow resistance due to increased electrical attraction on counter ions, a highly basic solution with a high EDL potential magnitude results in a significant decrease in the slip length. Neglecting the effect of SCDS leads to an overestimation of flow velocity, with this overprediction being more pronounced for highly basic solutions. This overestimation diminishes as bulk salt concentration increases, particularly when compared to strongly acidic solutions. Furthermore, a noticeable increase in average velocity is observed as the Deborah number rises for highly basic solutions compared to highly acidic ones. This is attributed to the substantial reduction in apparent viscosity caused by the shear-thinning nature of the liquid at higher shear rates, supported by a larger zeta potential modulated strong electrical force for basic solutions. Additionally, we found that the intensity of shear and normal stresses tends to increase with bulk pH, primarily due to the rise in electric body force at higher zeta potential. These results can potentially inform the design and development of a compact, nonmoving electroosmotic pump for transporting biological species with varying physiological properties, such as solution pH. This technology could be applied in subsequent processes involving mixing, separation, flow-focusing for cell sorting, and other related applications.

Influence of a Decrease in Blood Viscosity on Arterial Pressure in Normotensive and Spontaneously Hypertensive Rats.

We investigated the effect of a decrease in blood viscosity on the mean BP during isovolumic hemodilution and vasodilating activity of the endothelium in normotensive Wistar rats and spontaneously hypertensive rats (SHR). Blood viscosity was reduced by isovolumic hemodilution (replacement of 10% of circulating blood with an equal volume of plasma). Hemodilution caused the same reduction in blood viscosity by 16% in both groups of rats. In Wistar rats, a decrease in blood viscosity did not significantly change in the mean BP; no significant correlations between blood viscosity and mean BP were observed before and after hemodilution. In SHR, a decrease in blood viscosity led to a significant decrease in the mean BP by 18%. Correlations were found between the mean BP and blood viscosity in SHR before (r=0.63; p=0.028) and after (r=0.71; p=0.009) isovolumic hemodilution. In SHR, a decrease in the index of vasodilating activity of the endothelium due to a decrease in the vasodilatory response to intravenous administration of the endothelium-dependent vasodilator acetylcholine was revealed. In SHR, BP passively follows the change, in this case, the decrease in blood viscosity, which attests to impaired BP regulation in response to changes in shear stress on the vascular endothelium caused by the development of endothelial dysfunction in hypertensive animals.

Preparation and Application of Silane-Modified Polycarboxylate Superplasticizer in Concrete Viscosity Reduction

To address the issue of high viscosity in the construction of high-performance concrete, researchers have developed silane-modified micro-cross-linked polycarboxylate superplasticizers (SPCEs) through free radical-initiated copolymerization. These SPCEs have been studied for their molecular structure, adsorption behavior in cement paste, and influence of silane content on rheological performance of cement paste and concrete. The experimental findings indicate that while SPCEs exhibit a slightly diminished water reduction rate, the viscosity of cement paste with SPCEs is lower compared to conventional polycarboxylate superplasticizer with equivalent fluidity. This is attributed to their enhanced adsorption capacity, reduced intrinsic viscosity, and smaller hydrodynamic radius. Compared to the control group, the concrete made with SPCE showed a decrease of 23.53% and 11.00% in the outflow times of T500 and V-funnel, respectively, along with a reduction of 19.43% in plastic viscosity. The condensation of silanol can enhance the hydration of cement during the intermediate and final phases, leading to an improvement in the strength of concrete in later stages. There was an 8.79% increase in intensity at 28 days compared to the control group. Consequently, micro-cross-linked SPCEs possess significant prospects for advancement and can be employed in high-performing concrete.