Electron Viscosity Research Articles

Influence of cerium addition and redox state on silicate structure and viscosity

AbstractThe viscosities of Ce‐free and Ce‐bearing (∼1.3 mol%, ∼6.5 wt.% Ce2O3) soda lime silicate (window glass) melts were measured with respect to oxidation state. Experiments were performed isothermally using a concentric‐cylinder viscometer on melts equilibrated with successively reducing CO–CO2 gas mixtures within a gas tight vertical tube furnace at 1 atm. Viscosity measurement and sampling were performed at the end of each melt reduction step. Further, viscosities in the glass transition temperature range were estimated using the shift factor method applied to glass transition temperature values determined using differential scanning calorimetry (DSC) measurements on quenched glasses. The Ce speciation at each stepwise melt reduction was probed using Ce L3‐edge X‐ray absorption near‐edge structure (XANES) spectroscopy, while structural information upon Ce addition and reduction was provided by Raman spectroscopy. The viscosities of these materials remain constant at this level of Ce addition and do not vary significantly with redox state at high temperature. Conversely, viscosity values in the glass transition temperature range increase upon both Ce addition and reduction. Our analysis, based on the glass composition analyses obtained via electron probe microanalyzer (EPMA), viscosity calculations, and observations of silicate structural changes, leads to the conclusion that the observed viscosity increase around the glass transition temperature is explained by the high ionic field strength of Ce ions as well as the polymerization behavior of the silicate matrix occurring during reduction of Ce. Because of its low concentration, resulting from its low solubility, Ce redox changes exert only minimal effects on the viscosity of this melt.

Viscous Current-Induced Forces.

We study the motion (translational, vibrational, and rotational) of a diatomic impurity immersed in an electron liquid and exposed to electronic current. An approach based on the linear response time-dependent density functional theory combined with the Ehrenfest dynamics leads to a system of linear algebraic equations, which account for the competing and counteracting effects of the current-induced force (electron wind) and the electronic friction. We find and emphasize the coupling between the center of mass motion and that of the nuclei relative to each other, the feature due to the mediation of the two-body interaction by the environment. The current-induced forces, by means of the dynamic exchange-correlation (xc) kernel f_{xc}(r,r^{'},ω), include the electronic viscosity contribution. Starting from the ground state at the equilibrium internuclear distance and applying a current pulse, we observe three phases of the motion: (i)acceleration due to the prevalence of the current-induced force, (ii)stabilization upon balancing of the two forces, and (iii)deceleration due to the friction after the end of the pulse. At lower, but still metallic, electron densities, the dynamic xc contribution to the force significantly affects the acceleration (deceleration) at the first (third) phase of the process. For the Cs density (r_{s}≈6 a.u.), this correction amounts up to 40% in the rotation regime.

A numerical study of electron-magnetohydrodynamics tearing modes in parameter ranges of experimental interest

We perform a numerical study of the linear dynamics of tearing modes in slab incompressible electron-magnetohydrodynamics (EMHD) by considering some parameter ranges, which can be of interest for laboratory plasmas (e.g., helicon devices) or for astrophysics (e.g., solar-wind turbulence). To this purpose, several non-ideal effects are simultaneously retained (finite electron inertia, resistivity, and electron viscosity), and we make distinction between the dissipation coefficients in the direction parallel and perpendicular to the guide field. We thus identify some new reconnection regimes, characterized by a departure from the customary monotonic power-law scalings of the growth rates with respect to the non-ideal parameters. The results here presented can provide a useful indication for future studies of EMHD regimes relevant to experiments and for extensions of the EMHD tearing mode modeling to more complete regimes including kinetic effects (e.g., “electron-only” reconnection in kinetic regimes).

Design, synthesize, physicochemical characterization, nonlinear optical properties structural elucidation, biomedical studies, and DNA interaction of some new mixed ligand complexes incorporating 4,6‐dimethylpyrimidine derivative and imidazole ligand

This study was planned to prepare new mixed ligand chelates derived from N‐(4,6‐dimethylpyrimidin‐2‐yl)‐3a,4,5,6,7,7a‐hexahydro‐1H‐benzimidazol‐2‐amine (BIP), and imidazole (I). They identified through CHN study, spectroscopic (NMR, FT‐IR, and UV–Vis), conductivity, magnetic susceptibility, mass analysis, and thermal analysis. Correlation between all results exposed that the BIP ligand performed as a bi‐dentate ligand through NN donation locations, where the co‐ligand shows as N–H monodentate. The optimization for the studied chelates led to the formation of distorted octahedral geometry for BIPICu and BIPIVO chelates, distorted (tetrahedral and square planar) geometry for BIPIAg and BIPIPd chelates, respectively, around the metal salt. The B3LYP level, B3LYP/6‐311G** level for the free ligand, and B3LYP/6–311G**‐LANL2DZ functional level for the solid chelates were used in density functional theory (DFT) calculations. The findings showed that DFT calculations produce conclusions that are consistent with those of the experiments. The resulting compounds' nonlinear optical properties were examined by calculating the hyperpolarizability (β) and molecular polarizability (α) parameters, which gave rise to several unexpected optical properties for the synthesized compounds. Using the agar well diffusion method, the antimicrobial activity of the produced compounds was experimentally confirmed against a subset of G+ and G− bacteria. To ascertain how these substances attach to the targeted protein binding sites, a molecular docking mechanism between the microbially resistant chelates and their suppressed microbial protein pocket receptors was investigated. Also, DNA binding estimated for studied structures was tested by electronic absorption spectrum, viscosity estimation, and gel electrophoresis. Data proposed that all tested compounds link with DNA using an intercalation, electrostatic, and covalent binding mechanism. Moreover, antioxidant performance for studied compounds was governed by radical scavenging techniques in vitro. In addition, an MTT assay has been worked out to explore in vitro cytotoxic impending. All the tested chelates assumed antimicrobial, antitumor, and antioxidant performances that cause them to suggest drugs.

Synthesis, characterization of Schiff base metal complexes with 1, 3 propanediamine as secondary chelates and their DNA binding, DNA cleavage, cytotoxicity, antioxidant and activities

A series of Cu(II), Co(II), Ni(II), and Zn(II) complexes were synthesised from ternary Schiff base ligand (ts) and 1,3-propanediamine (pda). These complexes were characterised using analytical and spectroscopic techniques. All these metal complexes have an octahedral geometry, which is supported by spectro-analytical experimental data. The fabricated Schiff base coordinates with the metal via imine nitrogen, a phenolic oxygen atom, and carboxylate anion as a monobasic tridentate. Thermal properties were also investigated. Antimicrobial studies were carried out against fungi and pathogenic (bacterial) organisms and a good zone of inhibition was observed irrespective of complexes. Free radical scavenging assays were performed by DPPH and H2O2 methods. The results of these two studies revealed that the Cu(II) and Zn(II) complexes were more active. The binding mode of calf thymus (Ct-DNA) to the metal complexes was analysed by the electronic absorption spectroscopy and viscosity measurement study. The findings revealed that the complex bound with DNA via a groove with electrostatic interactionand the copper complex showed a higher binding constant value. Cytotoxicity of the Schiff base and its complexes were evaluated with the breast cancer (MCF-7) cell line and all complexes exhibited moderate toxicity.

The rheological response of magma to nanolitisation

Viscosity exerts a fundamental control on magmatic kinetics and dynamics, controlling magma ascent, eruptive style, and the emplacement of lava. Nanolites – crystals smaller than a micron – are thought to affect magma viscosity, but the underlying mechanisms for this remain unclear. Here, we use a cylinder compression creep technique to measure the viscosity of supercooled silicate liquids with different amounts of iron (0–20 wt% FeOtot) as a function of temperature, applied shear stress, and time. Sample viscosity was independent on the applied shear stresses, and as expected, melt viscosity decreases as temperature is increased, but only until a critical temperature where a time-dependent increase in viscosity occurs for samples contaning 6.0 wt% FeOtot or more. The magnitude of this increase is controlled by the melt iron content. At constant temperature, these changes are substantial and can reach up to three orders of magnitude for the sample with the most iron. Using transmission electron microscopy, X-ray diffraction, and viscosity modelling, we conclude that this viscosity increase is caused by the formation of nanolites. By using scaling approaches to test suspension effects with and without crystal aggregation, we conclude that the nanolites have only a minimal direct physical effect on the observed viscosity change. Rather, our models show that it is the chemical shift in the groundmass silicate melt composition associated with non-stoichiometric crystallisation that dominates the observed viscosity increase. These findings suggest that iron-rich silicates may encounter chemical viscosity jumps once certain elements are removed from the melt phase to form nanolites. Our work demonstrates an underlying mechanism for the role played by nanolites in viscosity changes of magmas.

Effects of electron viscosity on resonant layer responses to non-axisymmetric magnetic perturbations

The resonant field penetration to magnetic islands is the central MHD mechanism of non-axisymmetric plasma responses in a tokamak such as disruptive locking or favorable ELM stabilization. The resonant field penetration can be induced by any non-ideal processes as manifested in the delicate balance under the generalized Ohm's law. Here, we show that the viscous effects by electrons are not ignorable in the field penetration unlike previous presumption, even if the electron viscosity is as small as the square root of its mass compared to the ions. It is clear that its effects become only bigger if the electron viscosity becomes anomalously large. The work strictly follows the three-field model in the linear regime targeting the prediction of the onset of the field penetration and successfully extending it with electron viscosity and identifying new regimes. The results also indicate that the error field thresholds become more strongly dependent on plasma density than ones predicted in the linear regimes without the electron viscosity, which is consistent with experimental observations and thus a significant implication.

A yeast-malic acid crosslinker/polyacrylic acid hydrogel containing doxycycline for the treatment of periodontitis.

Doxycycline (DX) is a drug of choice for the treatment of periodontitis, with the limitation of requiring a high dose, which may be overcome by the preparation of a targeted controlled-release hydrogel containing a newly synthesized yeast-malic acid crosslinker (YMC). YMC was synthesized via thermochemical modification of yeast with malic acid at 100-140 °C and compared with glutaraldehyde-saturated toluene (GST). Swelling capacity, acid and carboxyl content, scanning electron microscopy (SEM) imaging, Brunauer-Emmett-Teller (BET) analysis, viscosity, cross-linking density, DX loading and release behavior at pH 6.5, mucoadhesion, and antimicrobial and periodontal efficacy of the glutaraldehyde hydrogel (HGG) and YMC hydrogel (HGY) were compared. Changes from C-O (1421 cm-1) to C[double bond, length as m-dash]OOR (1702 cm-1) in the infrared spectroscopy, along with changes in the degree of substitution from 0 to 0.39, degree of esterification from 0 to 40 ± 1.5 and COOH content from 129 ± 0.5 to 290 ± 0.5 (meq. per 100 g), were found between yeast to YMC, respectively. The results revealed 1.5 times more dynamic swelling, 0.25-fold decrease in acid content, 2.3-fold increase in carboxyl content, and 1.2- and 2.1-fold increases in cross-linking density and viscosity of HGY as compared to HGG, respectively. The SEM and BET results revealed that HGY had a 2 times greater porous surface than HGG. HGY/DX was 35 ± 2% more effective in controlling periodontitis bacteria, decreased periodontal depth from 4 to 3.2 mm, and gingival index from 3 to 1 as compared to HGG/DX in patients suffering from periodontitis. HGY/DX not only serves as a tool for the controlled release of DX in periodontal pockets but also contributes to the treatment of gingival periodontitis.

The Study of Interaction Activity of Nickel (ll) Phthalocyanine Complex Bearing Tetra Substituted Phenoxy-3-Methoxybenzoic Acid Groups with DNA

Nickel phthalocyanine complex containing 3-methoxybenzoic acid groups was acquired and specified by way of Fourier Transform Infrared, NMR and UV-Visble spectroscopy procedures. Interaction of PcNi with the DNA molecule was examined via electronic absorption spectra, fluorescence spectra, melting point, viscosity, and the electrophoresis technics, respectively. The interaction activity of PcNi against the DNA was examined by way of absorption spectra titrations and the fluorescence spectra, farther by conducting melting point, viscosity procedures in the buffer of a pH 7.02. The obtained outcomes from these methods demonstrated that PcNi indicated substantial binding affinity to the DNA via intercalating by Kb of 1.31 x 106 m-1. Further, the interacting activity of PcNi on the DNA was analyzed by which electrophoresis technique and this procedure indicated that PcNi complex exhibits strong binding affinity on the DNA.

Asymptotic scalings of fluid, incompressible “electron-only” reconnection instabilities: Electron-magnetohydrodynamics tearing modes

We perform a numerical study of the scaling laws of tearing modes in different parameter regimes of incompressible fluid electron magnetohydrodynamics, both in the small and large wavelength limits, as well as for the fastest growing mode that can be destabilized in a large aspect ratio current sheet. We discuss the relevance of these results, also for the interpretation of the “electron-only reconnection regime,” recently identified in spacecraft measures and in numerical simulations of solar wind turbulence. We restrict here to a single parameter study, in which we selectively consider only one non-ideal effect among electron inertia, perpendicular resistivity, and perpendicular electron viscosity, and we also consider the cases in which a proportionality exists between the parallel and the perpendicular dissipative coefficients. While some known theoretical results are thus confirmed, in other regimes and/or wavelength limits, corrections are proposed with respect to some theoretical estimates already available in the literature. In other cases, the scalings are provided for the first time. All numerical results are justified in terms of heuristic arguments based on the measurement of the scaling laws of some new microscopic scales associated with the gradients of the eigenfunctions. The alternative scalings we have found are consistent with this interpretation.

Exploring the Blends' Miscibility of a Novel Chitosan Derivative with Enhanced Antioxidant Properties; Prospects for 3D Printing Biomedical Applications.

Chitosan is a polysaccharide vastly examined in polymer science for its unique structure. In the present study, CS was derivatized with 2-methoxy-4vinylphenol (MVP) in four different ratios through a free radical reaction. The CS-MVP derivatives were characterized through FTIR, 1H-NMR, XRD, swelling, and solubility measurements. Owing to the enhanced antioxidant character of the MVP monomer, the antioxidant activity of the CS-MVP derivatives was assessed. In the optimum CS-MVP ratio, blends between CS and CS-MVP were prepared in ratios of 90:10, 80:20, 70:30, 60:40, 50:50, 40:60, 30:70, 20:80, and 10:90 w/w, and their miscibility was examined by scanning electron microscopy (SEM) and viscosity measurements. In the optimum ratios, highly concentrated inks were prepared, and their viscosity measurements revealed the successful formation of highly viscous gels with shear thinning behavior. These inks could be appropriate candidates for biomedical and drug delivery applications.

Structural, spectral and biological studies of (E)-2-((2-(benzo[d]thiazol-2-yl)hydrazineylidene)methyl)-4,6-dibromophenol (HL) and its metal complexes of Mn(II), Cu(II), Co(II), Ni(II), and Zn(II)

In this article there are five mononuclear complexes were discovered, 1. [Mn(II)(2-BHMBP)2], 2. [Cu(II)(2-BHMBP)2], 3. [Co(II)(2-BHMBP)2], 4. [Ni(II)(2-BHMBP)2] and 5. [Zn(II)(2-BHMBP)2] utilising a Imine base ligand, HL C14H9Br2N3OS (E)-2-((2-(benzo[d]thiazol-2-yl)hydrazineylidene)methyl)-4,6-dibromophenol were prepared and structurally characterised by the FT-IR spectra (vibrational spectroscopy), Proton NMR (1H NMR) spectroscopy, Carbon NMR (13C NMR) spectroscopy, ESI- Mass, SEM, EDX, powder XRD, TGA and ESR/EPR strategies. The complexes preliminary Deoxyribonucleic acid (DNA) binding activity was investigated by electronic absorption, fluorescence and viscosity spectroscopy in the presence of Calf thymus-DNA (CT-DNA). Using the agarose gel electrophoresis method in the presence of H2O2, DNA photo cleavage studies were performed on all metal complexes. The MTT assay was utilized to assess the cytotoxicity of all the compounds against two human cancer cell lines: HeLa and MCF-7. The compounds along with ligand have been screened for antifungal activity against fungal species Candida albicans and it is found that all Complexes are more potent than free ligand.

Physicochemical characterization of titanium dioxide inks for digital textile printing based on newly developed polyurethane prepolymers

Purpose This paper aims to study the physical and chemical characteristics of inkjet titanium dioxide inks for cotton fabric digital printing. Design/methodology/approach Different dispersing agents through the reaction of glycerol monooleate and toluene diisocyanate were prepared and then performed by using three different polyols (succinic anhydride-modified polyethylene glycol PEG 600, EO/PO Polyether Monoamine and p-chloro aniline Polyether Monoamine), to obtain three different dispersing agents for water-based titanium dioxide inkjet inks. The prepared dispersants were characterized using FTIR to monitor the reaction progress. Then the prepared dispersants were formulated in titanium dioxide inkjet inks formulation and characterized by particle size, dynamic surface tension, transmission electron microscopy, viscosity and zeta potential against commercial dispersants. Also, the study was extended to evaluate the printed polyester by using the prepared inks according to washing and crock fastness. Findings The obtained results showed that p-chloro aniline Polyether Monoamine (J) and succinic anhydride modified polyethylene glycol PEG 600 (H) dispersants provided optimum performance as compared to commercial standards especially, particle size distribution data while EO/PO Polyether Monoamine based on dispersant was against and then failed with the wettability and dispersion stability tests. Practical implications These ink formulations could be used for printing on cotton fabric by DTG technique of printing and can be used for other types of fabrics. Originality/value The newly prepared ink formulation for digital textile printing based on synthesized polyurethane prepolymers has the potential to be promising in this type of printing inks, to prevent clogging of nozzles on the printhead and to improve the print quality on the textile fiber.

Physical and Chemical Investigation of TiO2 Nanotubes Treated with Isopropyl Triisostearoyl Titanate (KR-TTS)

The aim of this study is to investigate the effect of isopropyl triisostearoyl titanate (KR-TTS) as a titanate coupling agent (TCA) on surface modification of TiO2 nanotube (TNT) material. From the physical and chemical studies that have been performed on the modified TiO2 nanotube, scanning electron microscope micrographs, energy-dispersive X-ray and viscosity indicated that there was significant reduction in particle aggregation of the modified TiO2 Nanotube. FTIR spectroscopy confirmed that the functional group of the TCA reacted with the hydroxyl groups present on the surface of TiO2 nanotube resulting in an altered surface property from being hydrophilic to hydrophobic. X-ray diffraction indicated that crystalline structure did not change upon the modification with the coupling agent. Isopropyl triisostearoyl titanate (KR-TTS) is found to be superior in performance and has a significant effect on the dispersion and resolving of agglomeration. This paper presents the effect of surface modification with the TCA of isopropyl triisostearoyl titanate (KR-TTS) type on the TiO2 nanotube material.

Development of Copper Complexes with Diimines and Dipicolinate as Anticancer Cytotoxic Agents.

Coordination complexes may act as anticancer agents. Among others, the formation of the complex may facilitate the ligand uptake by the cell. Searching for new copper compounds with cytotoxic activity, the complex Cu-dipicolinate was studied as a neutral scaffold to form ternary complexes with diimines. A series of [Cu(dipicolinate)(diimine)] complexes (where diimine: Phenanthroline, phen, 5-NO2-phenanthroline, 4-methyl-phenanthroline, neocuproine, 3,4,7,8-tetramethyl-phenanthroline, tmp, bathophenanthroline, bipyridine, dimethyl-bipyridine, as well as the ligand 2,2-dipyridil-amine, bam) were synthesized and characterized both in the solid state, including a new crystal structure of [Cu2(dipicolinate)2(tmp)2]·7H2O. Their chemistry in aqueous solution was explored by UV/vis spectroscopy, conductivity, cyclic voltammetry, and electron paramagnetic resonance studies. Their DNA binding was analyzed by electronic spectroscopy (determining Kb values), circular dichroism, and viscosity methods. The cytotoxicity of the complexes was assessed on human cancer cell lines MDA-MB-231, MCF-7 (breast, the first triple negative), A549 (lung epithelial) and A2780cis (ovarian, Cisplatin-resistant), and non-tumor cell lines MRC-5 (lung) and MCF-10A (breast). The major species are ternary, in solution and solid state. Complexes are highly cytotoxic as compared to Cisplatin. Complexes containing bam and phen are interesting candidates to study their in vivo activity in triple-negative breast cancer treatment.

Synthesis, spectral, DFT calculation, antimicrobial, antioxidant, DNA/BSA binding and molecular docking studies of bio-pharmacologically active pyrimidine appended Cu(II) and Zn(II) complexes

A new pyrimidine derivative Schiff base (HL) [HL = 2-((4-amino-6-chloropyrimidin-2-ylimino)methyl)-4-nitrophenol] has been synthesized using 2,6-diamino-4-chloropyrimidine and 5-nitrosalicylaldehyde. Transition metal complexes of Cu(II) and Zn(II) complexes [CuL(OAc)] (1), [ZnL(OAc)] (2) are prepared with HL/metal(II) acetate with molar ratio of 1:1. The Schiff base (HL) and the complexes 1 and 2 are evaluated by UV-Visible, 1H-NMR, FT-IR, EI-MS and ESR spectral techniques. Complexes 1 and 2 are confirmed as square planar geometry. Electrochemical studies of the complexes 1 and 2 are used to analyse the quasi reversible process. Density Functional Theory (DFT) using the B3LYP/6-31++G(d,p) level basis set was used to get the optimised geometry and non-linear optical properties. The complexes 1 and 2 are good antimicrobial agents than Schiff base (HL). The interactions of the HL and complexes 1 and 2 with Calf Thymus (CT) DNA are investigated by electronic absorption methods and viscosity measurements. Various molecular spectroscopy techniques, such as UV absorption and fluorescence, were used to explore the mechanism of interaction between the BSA and the ligand HL and complexes 1 & 2 under physiological settings. Complexes 1 and 2 are act as potential antioxidants than free Schiff base (HL) by DPPH radical scavenging assay. Furthermore, the purpose of the molecular docking studies was to better understand how metal complexes interact with biomolecules (CT-DNA and BSA). From these biological analyses, complex 1 acts as good intercalator with CT DNA & BSA and potent antioxidant with DPPH radical than complex 2. Communicated by Ramaswamy H. Sarma

Electrospun sandwich-structured of polycaprolactone/gelatin-based nanofibers with controlled release of ceftazidime for wound dressing

In the present work, sandwich-like polycaprolactone/gelatin/polycaprolactone electrospun multilayered mats were implemented to control the release of ceftazidime (CTZ). The outer layers were made from polycaprolactone nanofibers (NFs), and CTZ-loaded gelatin provided an internal layer. The release profile of CTZ from mats was compared with monolayer gelatin mats and chemically cross-linked GEL mats. All the constructs were characterized using scanning electron microscopy (SEM), mechanical properties, viscosity, electrical conductivity, X-ray diffraction (XRD), and Fourier transform-infrared spectroscopy (FT-IR). In vitro cytotoxicity against normal fibroblasts as well as antibacterial activity of CTZ-loaded sandwich-like NFs were investigated by the MTT assay. The results showed that the drug release rate from the polycaprolactone/gelatin/polycaprolactone mat was slower than that of gelatin monolayer NFs, and the rate of release can be adjusted by changing the thickness of hydrophobic layers. The NFs exhibited high activity against Pseudomonas aeruginosa and Staphylococcus aureus, while no significant cytotoxicity was observed against human normal cells. Altogether, the final mat as a predominant antibacterial scaffold can be used for controlled drug release of antibacterial drugs as the wound healing dressings in tissue engineering.

Electronic viscosity and energy relaxation in neutral graphene

We explore hydrodynamics of Dirac fermions in neutral graphene in the Corbino geometry. In the absence of a magnetic field, the bulk Ohmic charge flow and the hydrodynamic energy flow are decoupled. However, the energy flow does affect the overall resistance of the system through viscous dissipation and energy relaxation that has to be compensated by the work done by the current source. Solving the hydrodynamic equations, we find that local temperature and electric potential are discontinuous at the interfaces with the leads as well as the device resistance and argue that this makes Corbino geometry a feasible choice for an experimental observation of the Dirac fluid.

Enhanced oil recovery in fractured low-permeability reservoirs by a novel gel system prepared by sustained-release crosslinker and water-soluble thixotropic polymer

Polymer gels have been widely used in improving oil recovery and decreasing excessive water production in heterogeneous reservoirs after the long-term water flooding process. However, the high initial viscosity of polymer and the short gelation time still restricts the performance of polymer-based in situ cross-linked gels for in-depth conformance control. Herein, a novel gel system formed by in-situ crosslinking of water-soluble thixotropic polymer (WTP) and sustained-release crosslinker (SRC) was proposed. The WTP was synthesized by acrylamide, 2-acrylamido-2-methylpropanesulfonic acid, and N-[3-(dimethylamino)propyl] methacrylamide. It exhibits low viscosity under high shear rates and becomes thick under low shear rates, which ensures good injectability during the injection process and high gelation strength after cross-linking. The SRC was prepared by coating poly(ethyleneimine) (PEI) into the W/O/W multiple emulsions. The sustained-release mechanisms were well elaborated by confocal laser scanning microscopy (CLSM) observations. Only after the demulsification of multiple emulsions, the PEI would be released from the internal aqueous phase to the external aqueous phase. Therefore, these emulsions can be employed to deliver crosslinkers to specified targets in deep regions and prolong the release of crosslinkers to prevent undesirable crosslinking reactions near the injecting wells. According to the environmental scanning electron microscope (ESEM) observations and viscosity measurements, the low viscosity and an incompact spatial network could be observed in SRC/WTP gel system in the first 17 d, after which the PEI molecules were released to the external aqueous phase and cross-linked with WTP, forming the solid gel with small pores and yielding a high viscosity of 8793 mPa⋅s. Rheology tests have demonstrated that the elastic modules and the liner viscoelastic region of the novel gel system was nearly two times and twenty times than the traditional polymer gel, indicating higher gelation strength and better shear resistance. The core flooding tests showed that the SRC/WTP gel system had good injectability and could effectively plug the millimeter and submillimeter-sized cracks in low-permeability cores. 0.6 pore volume (PV) of SRC/WTP gel system with 3 gel slugs and a low injection rate can yield the best plugging performance in fractured core samples. And the gelation time shortens with the decrease of fracture apertures. Most importantly, the field tests in Ordos Basin verified the desirable EOR performance of the SRC/WTP gel system in fractured low-permeability reservoirs.

Нестационарные одномерные течения электронов в гидродинамическом режиме

In this paper, we consider the motion of electrons in a constant electric field in a certain temperature range, when the motion can be described by an equation of the Darcy–Brinkman type. We studied the on-set of the stationary current flow in a conductor with and without taking into account the viscosity of elec-trons after switching on a longitudinal electric field. Solutions with an alternating electric field and a solu-tion in the form of a traveling wave are also considered. In addition, we analyzed small perturbations of the stationary flow by the Galerkin method, which confirmed that the flow is stable at parameters corre-sponding to the flow of current through the conductor.