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Ionization processes of negative corona discharge. Part 2. Theory. Comparison with experiment 负电晕放电的电离过程。第 2 部分。理论。与实验的比较
Pub Date : 2024-07-02 DOI: 10.21869/2223-1528-2024-14-2-122-141
A. I. Zhakin, A. E. Kuzko
   The purpose of the research is a theoretical analysis of ionization processes in the air, which are initiated by a high-voltage field generated by the negative needle-flat electrode electrode system.   Methods. Fe, Cu, Al electrodes are used. Calculations are carried out using the methods of quantum mechanics and mathematical physics.   Results. The processes of cold and thermoelectron emission of electrons, enhanced by an external high-voltage field (Schottky emission), are analyzed. The conditions under which the generation of charges from the cathode surface due to plasma-chemical reactions and the capture of surface electrons by electronegative oxygen molecules are decisive are investigated. Based on the PE theory, a theory of injection of negative ions from the cathode into an electronegative gas is constructed and the theory is compared with experiment. It has been shown that at small radii of curvature of needle tips, when E ≥ 106 V/cm, the generation of charges is due to cold emission of electrons. In average fields E ≈ 105 V/cm, electron emission is due to the Schottky effect. In fields E ≈ 104 V/cm and below, injection is caused by electrochemical processes and PE capture. A theory has been developed for PEs that appear at electric field intensities on the electrode of the order of several tens of kV/cm, that is, on flat and slightly curved negative electrodes. The capture of PE by electron-withdrawing molecules causes an injection current and, as a consequence, the ignition of a corona discharge. Analytical expressions for the surface density as a function of the local electric field strength, as well as an expression for the injection current, are obtained. The agreement between theory and experiment is satisfactory.   Conclusion. An analysis of the development of CR on negative needles is given. A theory of PE at the cathode in strong electric fields was developed. Based on the results of measuring dark negative current-voltage characteristics, it is possible to determine the patterns of surface processes involving electronic transitions, in particular, determine the concentration of PE and injection currents.
研究的目的是对空气中的电离过程进行理论分析,该过程是由负针扁平电极系统产生的高压场引发的。 研究方法使用铁、铜、铝电极。使用量子力学和数学物理方法进行计算。 结果分析了电子在外部高压场(肖特基发射)作用下的冷发射和热电子发射过程。研究了等离子化学反应导致阴极表面产生电荷以及负电性氧分子捕获表面电子的决定性条件。以 PE 理论为基础,构建了负离子从阴极注入电负性气体的理论,并将该理论与实验进行了比较。实验表明,在针尖曲率半径较小时,当 E ≥ 106 V/cm 时,电荷的产生是由于电子的冷发射。在平均电场 E ≈ 105 V/cm 时,电子发射是由于肖特基效应。在 E≈104 V/cm 及以下的电场中,注入是由电化学过程和聚乙烯俘获引起的。对于在电极上电场强度为几十千伏/厘米时出现的 PE,即在平坦和略微弯曲的负电极上出现的 PE,我们已经建立了一套理论。电子吸收分子捕获 PE 会产生注入电流,从而引发电晕放电。研究获得了表面密度与局部电场强度的函数分析表达式以及注入电流表达式。理论与实验之间的一致性令人满意。 结论分析了负针上 CR 的发展。提出了强电场下阴极 PE 的理论。根据测量暗负极电流-电压特性的结果,可以确定涉及电子转变的表面过程模式,特别是确定 PE 和注入电流的浓度。
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引用次数: 0
Behavior of magnetic systems of different dimensions in a magnetic field 不同尺寸的磁性系统在磁场中的行为
Pub Date : 2024-07-02 DOI: 10.21869/2223-1528-2024-14-2-142-155
E. Shel'deshova, E. V. Bondar, I. A. Shabanova, A. Churaev, E. A. Sokolov, K. A. Matarykin, P. Ryapolov
   Purpose. To investigate the influence of the magnetic field on the formation of structures in magnetic media of various dispersities.   Methods. Experiments to study the dynamics of magnetic inclusions were carried out on a self-made installation in flat transparent cells by microscopy. The magnetic field was created by an electromagnet FL-1 connected to a power source. Magnetite particles of various sizes, as well as metal balls with a diameter of 0.5 mm, were studied as a magnetic medium. Video recording was performed using a MICMED WiFi 2000X 5.0 microscope.   Results. The dynamics of magnetic inclusions in a viscous liquid medium under the influence of a magnetic field, as well as under conditions of mechanical shear effects, have been studied. The influence of the magnetic field strength on the growth rate of chain structures, as well as on the angle of deflection under shear action, has been studied. A theoretical interpretation of the observed phenomena is proposed.   Conclusion. During the experiment, it was found that under the influence of a magnetic field, magnetic inclusions form chain structures. Their size, growth rate and dynamics depend on the physical parameters of the system and the external magnetic field. An intensive increase in the formation of chains of magnetic inclusions was detected at low and medium values of the magnetic field strength. An experimental dependence of the angle of deviation of chain structures from the equilibrium position on the magnetic field strength is obtained, which correlates with known theoretical data, on the basis of which a computational model is proposed. The results of the study can be used to visualize numerical calculations of the dynamics of dispersed systems under external influences.
研究目的研究磁场对不同分散度磁性介质中结构形成的影响。 方法。通过显微镜在自制的扁平透明细胞装置上进行了研究磁性夹杂物动态的实验。磁场由连接电源的电磁铁 FL-1 产生。研究将不同大小的磁铁矿颗粒以及直径为 0.5 毫米的金属球作为磁性介质。使用 MICMED WiFi 2000X 5.0 显微镜进行视频记录。 研究结果研究了粘性液体介质中的磁性夹杂物在磁场影响下以及机械剪切效应条件下的动态。研究了磁场强度对链结构增长速度以及剪切作用下偏转角度的影响。对观察到的现象提出了理论解释。 结论在实验过程中发现,在磁场的影响下,磁性夹杂物会形成链状结构。它们的大小、生长速度和动态取决于系统的物理参数和外部磁场。在低磁场强度和中等磁场强度下,磁性夹杂物链的形成会显著增加。实验得出了磁链结构偏离平衡位置的角度与磁场强度的关系,这与已知的理论数据相关,并在此基础上提出了一个计算模型。研究结果可用于分散系统在外部影响下动态的可视化数值计算。
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引用次数: 0
Characterization of Copper nanoparticles obtained in AOT reverse micelles using flavonoids as a reducing agent 以黄酮类化合物为还原剂在 AOT 反胶束中获得的纳米铜颗粒的特性分析
Pub Date : 2024-07-02 DOI: 10.21869/2223-1528-2024-14-2-168-179
Javid Rashidi, L. S. Ageeva, E. A. Fatyanova, N. A. Borsch
   Purpose of the study. To characterize copper nanoparticles obtained in reverse micelles of sodium bis-(2-ethylhexyl)-sulfosuccinate (AOT) using flavonoids: quercetin and rutin in comparison with traditional reducing agents - sodium borohydride and hydrazine.   Methods. Chemical synthesis of copper nanoparticles, spectrophotometry to determine the maximum of the plasmon absorption band of copper nanoparticles, electron transmission microscopy.   Results. The reduction of copper ions using flavonoids – quercetin and rutin – confirmed the possibility of obtaining copper nanoparticles in the Cu+2/AOT/isooctane system (AOT is sodium bis-(2-ethylhexyl)-sulfosuccinate, an anionic surfactant that forms the micelle shell). During the formation of nanoparticles, “plasmonic” absorption bands were observed in the electronic spectra in the region of 400-440 nm. In the case of the traditional reducing agent, sodium borohydride, absorption is observed in the region of (439 ± 3) nm, which can also be attributed to the “plasmonic band” of copper nanoparticles, but its intensity is very low, which indicates the formation of a small amount of copper nanoparticles. Using transmission electron microscopy. The average size of copper nanoparticles was determined: 7.1, 8.2 and 18.5 nm in the case of quercetin, rutin and hydrazine, respectively. From the histograms constructed from the results of electron transmission microscopy, it follows that the use of flavonoids as reducing agents makes it possible to reduce the average size of copper nanoparticles and narrow their size distribution.   Conclusion. Copper nanoparticles obtained in a reverse micellar solution of AOT in iso-octane using the flavonoids quercetin and rutin as a reducing agent have an average size of 7-8 nm and a narrower size distribution compared to reduction with hydrazine.
研究目的与传统还原剂--硼氢化钠和肼相比,对使用黄酮类化合物:槲皮素和芦丁在双(2-乙基己基)-磺基琥珀酸钠(AOT)的反向胶束中获得的纳米铜粒子进行表征。 方法。化学合成纳米铜粒子,分光光度法测定纳米铜粒子等离子体吸收带的最大值,电子透射显微镜。 结果利用黄酮类化合物(槲皮素和芦丁)还原铜离子,证实了在 Cu+2/AOT/isooctane 体系(AOT 为双-(2-乙基己基)-磺基琥珀酸钠,一种阴离子表面活性剂,可形成胶束外壳)中获得纳米铜粒子的可能性。在纳米粒子形成的过程中,电子光谱中出现了 400-440 纳米的 "等离子 "吸收带。在传统还原剂硼氢化钠的情况下,在(439 ± 3)纳米区域观察到吸收,这也可归因于纳米铜粒子的 "等离子带",但其强度非常低,这表明形成了少量的纳米铜粒子。使用透射电子显微镜。测定了纳米铜粒子的平均尺寸:槲皮素、芦丁和肼的平均粒径分别为 7.1、8.2 和 18.5 纳米。从根据电子透射显微镜结果绘制的直方图可以看出,使用黄酮类化合物作为还原剂可以减小纳米铜粒子的平均尺寸,缩小其尺寸分布。 结论使用黄酮类化合物槲皮素和芦丁作为还原剂,在异辛烷中的 AOT 反向胶束溶液中获得的纳米铜粒子的平均尺寸为 7-8 纳米,与使用肼还原相比,其尺寸分布更窄。
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引用次数: 0
On the diffusive model of C60 fullerene clusterization in liquids 论 C60 富勒烯在液体中聚合的扩散模型
Pub Date : 2024-07-02 DOI: 10.21869/2223-1528-2024-14-2-156-167
L. V. Elnikova, V. G. Shevchenko, A. P. Kuzmenko
   Purpose of research. The purpose of the study is to explain the mechanisms of clustering of fullerene molecules in liquid media observed using various structural nuclear -physical methods, as well as the interpretation of experimental data within the framework of a microscopic diffusion model.   Methods. The article gives a brief overview of the results of positron annihilation spectroscopy, small-angle neutron scattering, translucent electron microscopy, with which the geometric parameters of fullerene clusters in solutions were established. The theoretical method of research is the microscopic diffusion model “Limited diffusion aggregation”, which describes the kinetic processes of clusterization.   Results. The diffusion limited aggregation model displays adequately the mechanism of formation of C60 molecules in the form of fractal units in the volume of fluid, observed in experiments on positron annihilation spectroscopy and small-angle neutron scattering. The structural indicators of aggregate fullerene particles in carbon disulfide, o-Xylene, toluene, water and other solvents are analyzed. The properties of various diffusion models (the reaction limited aggregation model and the diffusion limited aggregation model) are considered and their combination in relation to the assessmentsof the kinetics of fullerene aggregation in solutions. A quantitative comparison of the results of the discussed models was carried out using the example of carbon disulfide.   Conclusion. The diffusion microscopic models adequately describe the phenomenon of fullerene aggregation in polar and non-polar solvents, which are recorded by various nuclear methods (positron annihilating spectroscopy and small-angle neutron scattering), the most reliable is the diffusion limited aggregation model, more than that, it is the basis of a numerical definition of structural structures parameters of units. Compared to neutron scattering, with the annihilation of positrons, in the aggregation of fullerene the [Ps–C60] molecular complexes participate in the clusterization, but this does not affect the change in the size of the cluster and the reliability of the results.
研究目的。研究的目的是解释利用各种结构核物理方法观察到的富勒烯分子在液体介质中的聚集机制,以及在微观扩散模型框架内对实验数据的解释。 研究方法文章简要概述了正电子湮灭光谱法、小角中子散射法和透射电子显微镜法的研究成果,通过这些方法确定了溶液中富勒烯团簇的几何参数。研究的理论方法是 "有限扩散聚集 "微观扩散模型,该模型描述了团聚的动力学过程。 研究结果扩散有限聚集模型充分显示了在正电子湮灭光谱和小角中子散射实验中观察到的 C60 分子在流体体积中以分形单元形式形成的机制。分析了二硫化碳、邻二甲苯、甲苯、水和其他溶剂中富勒烯聚合颗粒的结构指标。考虑了各种扩散模型(反应受限聚集模型和扩散受限聚集模型)的特性以及它们与评估溶液中富勒烯聚集动力学的结合。以二硫化碳为例,对所讨论模型的结果进行了定量比较。 得出结论。扩散微观模型充分描述了富勒烯在极性和非极性溶剂中的聚集现象,这些聚集现象是通过各种核方法(正电子湮灭光谱和小角中子散射)记录下来的,其中最可靠的是扩散受限聚集模型,而且它还是对单元结构参数进行数值定义的基础。与中子散射和正电子湮灭相比,在富勒烯的聚集过程中,[Ps-C60] 分子复合物参与了团聚化,但这并不影响团聚体大小的变化和结果的可靠性。
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引用次数: 0
Simulation of ordering and diffusion in CrxMoNbTaVW alloys within the framework of the N-body approach when specifying interatomic interactions 在指定原子间相互作用的 N-体方法框架内模拟 CrxMoNbTaVW 合金中的有序和扩散过程
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-88-107
V. N. Maksimenko, A. G. Lipnitskii, N. V. Malai, V. M. Emelyanov
   Purpose. Development of interatomic potentials for atomistic simulation of alloys based on refractory metals of the V-Cr-Nb-Mo-Ta-W system and atomistic simulation using these ordering and diffusion potentials in CrxMoNbTaVW alloys.   Methods. The development of the interatomic potentials of the V-Cr-Nb-Mo-Ta-W system was carried out within the framework of the 𝑁-body approach; To optimize the parameters of the potentials, the results of calculations within the framework of the electron density functional theory using the VASP software package were used as target values; the simulations of ordering and diffusion was carried out using methods of molecular dynamics and the developed We have previously used the combined method of molecular dynamics and the Monte Carlo method (MD+MK).   Results. Within the framework of the 𝑁-body approach, potentials are constructed that complement the V-Nb-Mo-W potential system that we built earlier to the V-Cr-Nb-Mo-Ta-W system. The constructed potentials predict the characteristics of alloys in good agreement with experimental data, CALPHAD data and density functional theory data. Using these potentials by the MD+MC method, CrxMoNbTaVW alloys were modeled, where 𝑥 = 0, 0.5, 1, 2 and 3, in the temperature range from 500 ºC to 2300 ºC. The MD+MC calculations and CALPHAD data agreed in the temperature and concentration regions containing one phase of BCC. At a temperature of 1000ºC, MD + MC calculations show the presence of a single BCC phase, which contradicts CALPHAD data, but is consistent with experimental data. The simulation showed that the atomic structure of the CrMoNbTaVW model alloy is self-sufficient to realize the diffusion of components without artificial introduction of vacancies. The absolute values of the diffusion coefficients of the components and the values of the effective activation energy of diffusion in a solid solution of CrMoNbTaVW were calculated for the first time by the method of molecular dynamics. Analysis of the calculated diffusion characteristics indicates that a diffusion mechanism is implemented in the CrMoNbTaVW alloy, which includes coordinated movement of atoms of various grades.   Conclusion. The development of methods for atomistic simulations of alloys based on refractory metals of the V-Cr-Nb-Mo-Ta-W system and the results of atomistic simulation of ordering and diffusion in CrxMoNbTaVW alloys have shown their importance for explaining and predicting heat resistance caused by diffusion processes in multicomponent alloys at high temperatures.
目的为基于 V-Cr-Nb-Mo-Ta-W 系难熔金属的合金的原子模拟开发原子间位势,并利用这些有序和扩散位势对 CrxMoNbTaVW 合金进行原子模拟。 方法。在𝑁体方法框架内开发了 V-Cr-Nb-Mo-Ta-W 系统的原子间势能;为了优化势能参数,使用 VASP 软件包在电子密度泛函理论框架内计算的结果作为目标值;使用分子动力学方法和开发的分子动力学方法(MD+MK)进行了有序和扩散模拟。 结果。在𝑁体方法的框架内,我们构建了 V-Nb-Mo-W 电位体系,并将其补充到 V-Cr-Nb-Mo-Ta-W 体系中。所构建的势能预测合金的特性,与实验数据、CALPHAD 数据和密度泛函理论数据非常吻合。通过 MD+MC 方法使用这些电位,在 500 ºC 至 2300 ºC 的温度范围内建立了 CrxMoNbTaVW 合金模型,其中 𝑥 = 0、0.5、1、2 和 3。MD+MC 计算结果和 CALPHAD 数据在含有 BCC 一相的温度和浓度区域内一致。在温度为 1000ºC 时,MD + MC 计算显示存在单一 BCC 相,这与 CALPHAD 数据相矛盾,但与实验数据一致。模拟结果表明,CrMoNbTaVW 模型合金的原子结构自给自足,无需人为引入空位即可实现成分扩散。首次利用分子动力学方法计算了 CrMoNbTaVW 固溶体中各组分扩散系数的绝对值和有效扩散活化能的值。对计算得出的扩散特性的分析表明,CrMoNbTaVW 合金中存在一种扩散机制,其中包括不同等级原子的协调运动。 结论基于 V-Cr-Nb-Mo-Ta-W 系难熔金属的合金原子模拟方法的开发以及 CrxMoNbTaVW 合金中有序和扩散的原子模拟结果表明,它们对于解释和预测多组分合金在高温下由扩散过程引起的耐热性具有重要意义。
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引用次数: 0
Magnetron carbon structures obtained by high-frequency magnetron sputtering in Argon and Nitrogen 在氩气和氮气中通过高频磁控溅射获得的磁控碳结构
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-71-87
A. P. Kuzmenko, A. I. Kolpakov, A. S. Sizov, V. M. Emelyanov, Y. A. Neruchev
   Purpose of research. Creation and characterization of carbon nanostructures by high-frequency magnetron sputtering from a carbon target in argon on a silicon substrate and in a reactive nitrogen environment, obtained on a Ni catalyst buffer layer.   Methods. High-frequency magnetron sputtering on a silicon substrate with changes in control parameters: sputtering time power and working gas pressure Ar and N. Research was carried out using X-ray phase analysis, atomic force microscopy and holographic microscopy, Raman scattering.   Results. The formation of carbon nanotubes, including single-walled ones, was confirmed by the method of Raman scattering of light along the lines ID 1363 and IG 1564 cm-1, as well as ωRDМ 308 and 227 cm–1. Using atomic force microscopic images, the fractal dimension of the nanofilms was calculated, which indicated their 3D nature. Based on X-ray phase analysis of magnetron nanofilms, the dimensions of the coherence region, texture, microdeformations and interplanar deformation distortions were determined.   Conclusion. In carbon magnetron nanofilms, deformations of both signs occur: both compressive (∆a < 0) and tensile (∆a > 0). Carbon magnetron nanofilms are represented, among other things, by single-walled carbon nanotubes, the chirality of which in an argon environment is (6, 6), and in a reactive mixture of nitrogen and argon on a Ni buffer layer (7, 7). It was discovered that in high-frequency magnetron mode, silicon carbide is formed in both inert and reactive environments.
研究目的。通过高频磁控溅射从氩气中的碳靶材在硅基底和活性氮环境中产生碳纳米结构并对其进行表征,在镍催化剂缓冲层上获得碳纳米结构。 方法:高频磁控溅射使用 X 射线相分析、原子力显微镜和全息显微镜、拉曼散射进行研究。 研究结果拉曼散射光线 ID 1363 和 IG 1564 cm-1,以及 ωRDМ 308 和 227 cm-1 的方法证实了碳纳米管(包括单壁碳纳米管)的形成。利用原子力显微镜图像计算出了纳米薄膜的分形维度,这表明它们具有三维性质。基于磁控纳米薄膜的 X 射线相分析,确定了相干区的尺寸、纹理、微变形和平面间变形扭曲。 结论在碳磁控纳米薄膜中会出现两种变形:压缩变形(∆a < 0)和拉伸变形(∆a > 0)。碳磁控管纳米薄膜主要以单壁碳纳米管为代表,单壁碳纳米管在氩气环境中的手性为(6, 6),在镍缓冲层上的氮和氩反应混合物中的手性为(7, 7)。研究发现,在高频磁控管模式下,碳化硅在惰性环境和反应环境中都能形成。
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引用次数: 0
Structure and properties of alloys based on electroerosive brass powder LS58-3 obtained in distilled water 基于在蒸馏水中获得的电蚀性黄铜粉末 LS58-3 的合金的结构和性能
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-45-54
E. V. Ageeva, L. S. Abolmasova, A. Pereverzev
   The purpose of this work was to study the microstructure and physico-mechanical properties of alloy blanks based on electroerosive powder brass of the LS58-3 brand obtained in distilled water.   Methods. To carry out the planned research, waste of the LS58-3 alloy was selected. Distilled water was used as the working fluid. In an experimental patented installation for producing powders, waste LS58-3 alloy was dispersed in distilled water with a load mass of 300 g. The following modes were used: capacitor capacity 45–65 μF; voltage at the electrodes from 150–200 V; pulse repetition rate 50–100 Hz. The preparation of new alloy blanks was carried out using an SPS 25-10 electric spark plasma sintering installation (ThermalTechnology, USA). The microstructure of new alloy workpieces was studied using an electron-ion scanning (raster) microscope QUANTA 600 FEG (Netherlands). The study of the porosity of workpieces of new alloys was carried out using an optical inverted microscope OLYMPUS GX51 (Japan). The study of microhardness of workpieces of new alloys was carried out using an automated microhardness tester AFFRI DM-8 (Vickers).   Results. Analysis of the microstructure showed that the sample has a fine-grained structure and a homogeneous surface. According to the obtained porosity analysis results, the sample has less than 1% pores, which is achieved thanks to the technology of spark plasma sintering of the powder. Analysis of the microhardness of the sample showed a significant increase in microhardness, which is explained by the presence of high-hard particles formed during quenching of metal vapor in the working fluid during dispersion.   Conclusion. The use of spark plasma sintering technology for electroerosive brass makes it possible to obtain blanks of new alloys with a practically non-porous structure, which leads to an increase in the hardness of the resulting blanks. The results of the conducted studies make it possible to recommend the use of the resulting powder as a starting material for the production of alloy blanks and to expand the scope of their practical application.
这项工作的目的是研究基于在蒸馏水中获得的 LS58-3 牌电蚀粉末黄铜合金坯料的微观结构和物理机械性能。 研究方法为了开展计划中的研究,选择了 LS58-3 合金废料。蒸馏水被用作工作液。在一个生产粉末的专利实验装置中,将废 LS58-3 合金分散在蒸馏水中,负载质量为 300 克。采用以下模式:电容器容量 45-65 μF;电极电压 150-200 V;脉冲重复率 50-100 Hz。新合金坯料的制备是使用 SPS 25-10 电火花等离子烧结装置(美国 ThermalTechnology 公司)进行的。使用电子离子扫描(光栅)显微镜 QUANTA 600 FEG(荷兰)研究了新合金工件的微观结构。使用光学倒置显微镜 OLYMPUS GX51(日本)对新型合金工件的孔隙率进行了研究。使用自动显微硬度计 AFFRI DM-8(维氏)对新合金工件的显微硬度进行了研究。 结果显示微观结构分析表明,样品具有细粒结构和均匀的表面。根据获得的孔隙率分析结果,样品的孔隙率小于 1%,这要归功于粉末的火花等离子烧结技术。样品的显微硬度分析表明,显微硬度显著增加,这是因为在分散过程中,工作液中的金属蒸汽在淬火过程中形成了高硬度颗粒。 结论使用火花等离子烧结技术生产电蚀黄铜,可以获得几乎无孔结构的新型合金坯料,从而提高坯料的硬度。根据研究结果,我们建议将所得粉末用作生产合金坯料的起始材料,并扩大其实际应用范围。
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引用次数: 0
Influence of external magnetic field on the viscosity of electrically conducting magnetic fluids 外磁场对导电磁性流体粘度的影响
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-55-70
K. Komilov, A. Q. Zarifzoda
   Purpose. Theoretical study of an external magnetic field on the discontinuous and bulk viscosity of electrically conductive magnetic fluids.   Methods. The method of molecular kinetic theory is used, which, using kinetic methods for single-particle and two-particle distribution functions, allows one to determine transfer mechanisms in electrically conductive magnetic fluids.When constructing kinetic mathematical electrically conductive magnetic fluids as multicomponent systems in which non-magnetic and magnetic subsystems are independent, magnetic particles and the stabilizer substance closely interact with each other.   Results. Based on algorithms of expressions for the coefficients of shear and volumetric viscosity, the observed mechanisms of translational and structural relaxation processes, a series of calculations was carried out depending on thecoefficients of stepwise and volumetric viscosity from the results of external magnetic fields, the volumetric structure of magnetic particles and the calculation of measured values in electrically conductive magnetic fluids based on mercury and a eutectic alloy of Gallium and India. It is shown that with increasing external magnetic fields, the coefficients of shear and bulk viscosity in electrically conductive magnetic fluids increase nonlinearly. An increase in the volume of elements of magnetic particles also leads to a nonlinear increase in the coefficients of abrupt and bulk viscosity.   Conclusion. The given calculations of the coefficients of shear and bulk viscosity depending on the principle of international dependence indicate that the use of metal constants in electrically conductive magnetic fluids leads to a noticeable decrease in their viscosity. It is shown that the results obtained, in good agreement with literature data, can be used for further development of the theory of transfer processes of electrically conductive magnetic fluids.
目的。理论研究外磁场对导电磁性流体的非连续粘度和体积粘度的影响。 方法。采用分子动力学理论的方法,利用单粒子和双粒子分布函数的动力学方法,可以确定导电磁性流体中的传递机制。当构建动力学数学导电磁性流体作为多组分系统时,其中非磁性和磁性子系统是独立的,磁性粒子和稳定物质彼此密切相互作用。 结果。根据剪切粘度和体积粘度系数的表达式算法、观察到的平移和结构弛豫过程的机制,根据外磁场的结果、磁性粒子的体积结构以及基于汞和镓与印度的共晶合金的导电磁性流体中测量值的计算结果,进行了一系列计算。结果表明,随着外磁场的增加,导电磁性流体中的剪切系数和体积粘度系数呈非线性增加。磁性微粒元素体积的增加也会导致突变系数和体积粘度系数的非线性增加。 结论根据国际依赖性原理对剪切粘度和体积粘度系数进行的计算表明,在导电磁性流体中使用金属常量会明显降低其粘度。结果表明,所获得的结果与文献数据非常一致,可用于进一步发展导电磁性流体传递过程的理论。
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引用次数: 0
Synthesis of Eu-doped TiO2 nanoparticles by hydrothermal method 水热法合成掺 Eu 的 TiO2 纳米粒子
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-108-121
I. V. Egelskii, M. A. Pugachevskii, E. A. Martynova, Y. A. Neruchev
   Purpose of research. Synthesis, characterization and comparison of the photocatalytic properties of europium-doped titanium dioxide nanoparticles.   Methods. Europium-doped titanium dioxide nanoparticles were synthesized via a hydrothermal method followed by post-treatment processes including washing and annealing. Characterization was conducted using transmission electron microscopy, X-ray phase analysis, and energy-dispersive analysis. The bandgap width of the nanoparticles was determined through diffuse reflectance spectroscopy. Photoluminescence properties were studied using scanning probe microscopy and Raman spectroscopy. The photocatalytic properties were studied by spectrophotometry to determine the degradation of methylene blue under ultraviolet radiation.   Results. Transmission electron microscopy identified the average particle sizes of europium-doped titanium dioxide. Using X-ray phase analysis, it was established that the nanoparticles were in the anatase phase regardless of the europium content percentage. Energy-dispersive spectroscopy confirmed the presence of the dopant in the samples. The photoluminescence intensity peak increased proportionally with the increase in europium content percentage. The strongest photocatalytic properties were exhibited at the lowest europium content among the samples studied.   Conclusion. Synthesized and processed europium-doped titanium dioxide nanoparticles with anatase polymorphic modification exhibit photoluminescent properties. The luminescence intensity depends on the concentration of europium in the particles, due to the formation of additional energy levels inside the band gap. The photocatalytic properties of europium-doped nanoparticles are significantly improved in comparison with samples synthesized without impurities. However, a europium concentration above 0,5% leads to the growth of structural defects that reduce the mobility of photogenerated charge carriers and creates a high energy barrier that prevents them from reaching the surface.
研究目的掺杂铕的二氧化钛纳米粒子的合成、表征和光催化性能比较。 方法。通过水热法合成掺铕的二氧化钛纳米粒子,然后进行清洗和退火等后处理。利用透射电子显微镜、X 射线相分析和能量色散分析进行了表征。纳米粒子的带隙宽度是通过漫反射光谱测定的。利用扫描探针显微镜和拉曼光谱研究了光致发光特性。通过分光光度法研究了光催化特性,以确定亚甲基蓝在紫外线辐射下的降解情况。 结果。透射电子显微镜确定了掺铕二氧化钛的平均粒径。通过 X 射线相分析,确定了无论铕含量百分比如何,纳米颗粒都处于锐钛矿相。能量色散光谱证实了样品中存在掺杂剂。光致发光强度峰随铕含量的增加而成正比增加。在所研究的样品中,铕含量最低的样品具有最强的光催化性能。 结论合成和加工的掺铕二氧化钛纳米颗粒具有锐钛矿多晶型修饰,具有光致发光特性。由于在带隙内形成了额外的能级,发光强度取决于颗粒中铕的浓度。与不含杂质的合成样品相比,掺杂铕的纳米粒子的光催化特性得到了显著改善。然而,铕的浓度超过 0.5%,就会产生结构缺陷,从而降低光生电荷载流子的迁移率,并形成高能量屏障,阻止它们到达表面。
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引用次数: 0
On the effectiveness of using carbamide-based salt baths for low-temperature cyanidation of improved carbon and alloy steels 使用碳酰胺盐浴对改良碳钢和合金钢进行低温氰化的有效性
Pub Date : 2024-07-01 DOI: 10.21869/2223-1528-2024-14-2-33-44
N. N. Kostin, V. I. Kolmykov, N. A. Kostin, D. V. Kolmykov
   Purpose. A study of cyanidation of improved carbon and alloy steels of grades 30, 30HGT, 30H13 at a temperature of 550–580 °C was carried out in baths based on carbamide and sodium carbonate. Recommendations on the use of these baths for surface hardening of carbon and alloyed improved steels used for the manufacture of machine parts are formulated.   Methods. The microstructure of the diffusion layer of steels on transverse sections was studied using a Quanta FEG – 650 electron scanning microscope with an EBCD focused ion beam microanalysis system. Cyanide wear tests were performed under friction conditions analogous to those of die tools. The wear resistance of the carbonitrided samples was investigated on a SMTs-2 friction machine. The tests were performed under both dry friction and boundary friction conditions.   Results. The high efficiency of the proposed bath composition at a given temperature has been experimentally shown. As a result of cyanidation, modified layers saturated with solid inclusions (ε-phases) are formed on the surface of steels, characterized by high hardness, low coefficient of friction and high wear resistance.   Conclusion. According to the results of the conducted research, it can be concluded that low-temperature cyanidation of improved steels of various grades can be carried out in cyanide-free salt baths. The optimal composition of the cyanide bath is 40% carbamide (NH2)2CO; 40 % soda ash Na2CO3 and 20 % NaCl table salt. The proposed bath does not contain toxic and scarce components, therefore it is environmentally safe and very cheap and can be used with great effect in machine-building, repair and tool industries.
研究目的对 30、30HGT、30H13 等牌号的改良碳钢和合金钢在 550-580 ℃ 的温度下在碳酰胺和碳酸钠浴中进行氰化的情况进行了研究。提出了使用这些浴液对用于制造机械零件的改良碳钢和合金钢进行表面硬化的建议。 方法。使用配备 EBCD 聚焦离子束显微分析系统的 Quanta FEG - 650 电子扫描显微镜研究了钢材横截面扩散层的微观结构。氰化物磨损试验是在类似于模具的摩擦条件下进行的。在 SMTs-2 摩擦机上对碳氮化样品的耐磨性进行了研究。测试在干摩擦和边界摩擦条件下进行。 结果显示实验表明,在给定温度下,所建议的熔池成分具有很高的效率。氰化的结果是在钢材表面形成了饱和固体夹杂物(ε相)的改性层,具有高硬度、低摩擦系数和高耐磨性的特点。 结论根据所进行研究的结果,可以得出结论:在无氰盐浴中可以对各种等级的改良钢进行低温氰化。氰化盐浴的最佳成分为 40% 的碳酰胺 (NH2)2CO、40% 的纯碱 Na2CO3 和 20% 的氯化钠食盐。拟议的盐浴不含有毒和稀缺成分,因此对环境安全,而且非常便宜,可在机械制造、维修和工具行业中广泛使用。
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Proceedings of the Southwest State University. Series: Engineering and Technology
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