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Influence of the Carbon Support on the Structural–Morphological Parameters and Electrochemical Properties of Platinum-Containing Catalysts for Fuel-Cell Cathode with a Proton-Exchange Membrane 碳载体对质子交换膜燃料电池阴极含铂催化剂的结构形态参数和电化学性质的影响
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167624600093
Yu. A. Bayan, K. O. Paperzh, I. V. Pankov, A. S. Pavlets, E. A. Moguchikh, A. A. Alekseenko

Finding the optimal substrate for electrocatalysts used as electrodes in fuel cells is an urgent task for the development of hydrogen energetics. The composition and the morphological and electrochemical properties of platinum–carbon catalysts synthesized according to a common method on various carbon supports (Vulcan XC-72, Vulcan XC-72R, Ketjenblack EC-300J, Ketjenblack EC-600JD, and modified Ketjenblack EC-600JD) and of a JM-20 commercial electrocatalyst are analyzed comparatively. It is found that highly dispersed supports (from 800 m2/g) make it possible to increase the catalytic activity of Pt/C materials in the electroreduction reaction of oxygen by two times compared to those with a specific surface area of less than 250 m2/g. The preliminary treatment of a carbon support with melamine increases the stability of catalysts based on it by 40%. A platinum-carbon catalyst with a 1.6-times-higher electrochemically active surface area and 1.7-times-higher mass activity in the reaction of oxygen electroreduction compared to a commercial analogue is obtained.

为燃料电池中用作电极的电催化剂寻找最佳基质是氢能源开发的一项紧迫任务。本文比较分析了在各种碳载体(Vulcan XC-72、Vulcan XC-72R、Ketjenblack EC-300J、Ketjenblack EC-600JD 和改性 Ketjenblack EC-600JD)上用普通方法合成的铂碳催化剂以及 JM-20 商用电催化剂的组成、形态和电化学特性。研究发现,与比表面积小于 250 m2/g 的铂/碳材料相比,高度分散的支持物(800 m2/g 以上)可将铂/碳材料在氧气电还原反应中的催化活性提高两倍。用三聚氰胺对碳载体进行初步处理,可使以碳载体为基础的催化剂的稳定性提高 40%。一种铂碳催化剂在氧气电还原反应中的电化学活性表面积和质量活性分别是商用同类催化剂的 1.6 倍和 1.7 倍。
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引用次数: 0
Interaction of Exogenous Nanoparticles of Refractory Phases with Surfactant Impurities of Non-ferrous Metals in Iron Melts in Contact with Refractory Material 与耐火材料接触的铁熔体中耐火相的外源纳米颗粒与有色金属表面活性剂杂质的相互作用
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601274
V. T. Burtsev, S. N. Anuchkin, A. V. Samokhin

Тhe results of the heterophase interaction of nanoparticles of refractory phases with iron melts containing harmful impurities (sulfur, antimony, tin, and copper) are studied and generalized. It is shown that the degree of the removal of impurities (~0.05 wt %) in the Fe–S, Fe–Sn, Fe–Sb, and Fe–Cu systems after the introduction of nanoparticles ranges from 10 to 37 rel %. As a result of the interaction of nanoparticles with impurities of the metal melt, the formation of ensembles with new surface properties is proposed. It is shown that the redistribution of ensembles in the melt and their removal to the phase interface can be represented as a two-stage process.

研究并归纳了难熔相纳米粒子与含有害杂质(硫、锑、锡和铜)的铁熔体的异相相互作用结果。结果表明,引入纳米粒子后,Fe-S、Fe-Sn、Fe-Sb 和 Fe-Cu 体系中杂质(约 0.05 wt %)的去除率为 10% 至 37%。由于纳米粒子与金属熔体中的杂质相互作用,形成了具有新表面特性的集合体。研究表明,集合体在熔体中的重新分布以及它们被移除到相界面的过程可以分为两个阶段。
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引用次数: 0
Impedance of Structures with Non-uniform Current Distribution 电流分布不均匀结构的阻抗
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601353
L. A. Shendrikova, N. S. Perov, N. A. Buznikov

The effect of giant magnetoimpedance in magnetic structure with inhomogeneous electric current distribution is studied. A special design reduces the magnitude of the intrinsic magnetic field outside the structure. The magnetoimpedance of such a planar structure made of magnetically soft material with radial current distribution has been investigated both theoretically and experimentally. The theoretical evaluations show a strong variation of the impedance of the structure with the frequency and the permeability value of the material. The results of calculations are qualitatively confirmed by experimental data for model samples.

摘要 研究了电流分布不均匀的磁性结构中的巨磁阻效应。一种特殊的设计降低了结构外的固有磁场的大小。我们从理论和实验两方面研究了这种由具有径向电流分布的磁性软材料制成的平面结构的磁阻。理论评估显示,结构的阻抗随频率和材料的磁导率值变化很大。模型样品的实验数据定性地证实了计算结果。
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引用次数: 0
Changes in the Microstructure and Electrochemical Behavior of Pt/C Electrocatalysts under Various Stress Testing Conditions 各种应力测试条件下 Pt/C 电催化剂微观结构和电化学行为的变化
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167624600081
E. A. Moguchikh, A. A. Alekseenko, I. V. Pankov, D. V. Alekseenko, V. E. Guterman

A comparative analysis of the microstructure and electrochemical behavior of platinum–carbon electrocatalysts containing 20 and 40% platinum from different manufacturers for fuel cells with a proton-exchange membrane is carried out. The degree of degradation of the catalysts during accelerated stress testing in laboratory conditions is assessed based on the results of not only residual functional characteristics, but also microstructural parameters after electrochemical tests. It is determined that 20 and 40% PM series catalysts contain smaller platinum nanoparticles, characterized by a narrower size and more uniform spatial distribution, compared to analogues of the HiSPEC series. Due to these microstructural features, a PM-series platinum–carbon catalysts are characterized by a higher electrochemically active surface area (EASA) and mass activity values initially and after stress testing.

摘要 对不同制造商生产的用于质子交换膜燃料电池的含 20% 和 40% 铂的铂碳电催化剂的微观结构和电化学行为进行了比较分析。在实验室条件下进行加速应力测试时,催化剂的降解程度不仅基于残余功能特性的结果,还基于电化学测试后的微观结构参数。结果表明,与 HiSPEC 系列催化剂相比,20% 和 40% PM 系列催化剂含有更小的铂纳米颗粒,其特点是尺寸更窄、空间分布更均匀。由于这些微观结构特征,PM 系列铂碳催化剂的电化学活性表面积(EASA)和质量活性值在初始和应力测试后都较高。
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引用次数: 0
Nanocomplexes of the Anthracycline Antibiotic Daunomycin and Doxorubicin with Selenium Nanoparticles and Polyvinylpyrrolidone: Spectral and Dimensional Characteristics 蒽环类抗生素 Daunomycin 和 Doxorubicin 与硒纳米颗粒和聚乙烯吡咯烷酮的纳米复合物:光谱和尺寸特征
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601560
A. I. Kipper, L. N. Borovikova, I. S. Garkushina

The influence of the hydroxyl group in the aglycone of the antitumor antibiotic doxorubicin on the spectrophotometric and dimensional characteristics of nanocomplexes of doxorubicin–polyvinylpyrrolidone–selenium nanoparticles is established. The involvement of components of ternary complexes in intermolecular interactions is assessed using the spectrophotometric method. The radii of gyration (40–60 nm) and hydrodynamic radii (20–70 nm) of the synthesized nanocomplexes are determined using static- and dynamic-light scattering methods. The hydroxyl group present in the structure of the antitumor antibiotic contributed to the formation in an aqueous environment of a more loose, permeable shell of the nanocomplex compared to the daunomycin–polyvinylpyrrolidone–selenium nanoparticles nanocomplexes. An increase in the Se concentration during the synthesis of nanocomplexes leads to expansion of the loose shell. The revealed patterns will further contribute to the development of methods for synthesizing nanocomplexes for the modification of water-soluble antitumor antibiotics.

摘要 确定了抗肿瘤抗生素多柔比星苷苷元中的羟基对多柔比星-聚乙烯吡咯烷酮-硒纳米粒子纳米复合物的分光光度和尺寸特征的影响。采用分光光度法评估了三元复合物各组分参与分子间相互作用的情况。利用静态和动态光散射法测定了合成纳米复合物的回旋半径(40-60 nm)和流体力学半径(20-70 nm)。与达霉素-聚乙烯吡咯烷酮-硒纳米粒子纳米复合物相比,抗肿瘤抗生素结构中的羟基有助于在水环境中形成更疏松、更易渗透的纳米复合物外壳。在合成纳米复合物的过程中,硒浓度的增加会导致松散外壳的扩张。所揭示的模式将进一步有助于开发用于改性水溶性抗肿瘤抗生素的纳米络合物的合成方法。
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引用次数: 0
Electron-Beam Deposition for the Synthesis of Memristive Structures Based on Hafnium Oxide 利用电子束沉积技术合成基于氧化铪的薄膜结构
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601523
B. S. Shvetsov, A. N. Matsukatova, M. N. Martyshov, D. M. Zhigunov, A. S. Ilyin, T. P. Savchuk, P. A. Forsh, P. K. Kashkarov

Нafnium oxide is currently considered one of the most promising metal-oxide materials for creating memristive structures. Memristive structures find their application in many areas of science and technology; for example, with their help, the biosimilar emulation of synapses in neuromorphic computing systems is possible. One of the important obstacles  to the industrial use of memristors is the variability of resistive switching. Nonstoichiometry in memristor structure can be an important tool for controlling resistive switching. Therefore, in this work, memristors based on hafnium oxide in a metal–insulator–metal sandwich structure are synthesized by electron-beam deposition, which makes it possible to create nonstoichiometric films. The effect of resistive switching is studied depending on the material of the upper electrode and the thickness of the hafnium-oxide layer. The synthesis parameters are determined to achieve a balance between the main memristive characteristics.

氧化铪目前被认为是最有前途的金属氧化物材料之一,可用于制造记忆结构。忆阻器结构在许多科技领域都有应用,例如,在它们的帮助下,神经形态计算系统中突触的生物仿真成为可能。忆阻器工业应用的一个重要障碍是电阻开关的可变性。忆阻器结构中的非均匀性可以成为控制电阻开关的重要工具。因此,在这项研究中,通过电子束沉积法合成了基于金属-绝缘体-金属夹层结构的氧化铪忆阻器,从而有可能制造出非化学计量薄膜。根据上电极的材料和氧化铪层的厚度,研究了电阻开关的效果。通过确定合成参数,实现了主要记忆特性之间的平衡。
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引用次数: 0
Improving the Electrochemical Properties of a Cathode Material Based on Lithium–Manganese Phosphate through the Partial Substitution of Mn for Ni 通过以锰部分替代镍改善基于磷酸锰锂的阴极材料的电化学特性
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167624600111
O. A. Drozhzhin, E. V. Zharikova, G. P. Lakienko, M. G. Rozova, E. V. Antipov

Lithium and transition-metal phosphates are promising cathode materials for lithium-ion batteries. Lithium manganese phosphate LiMnPO4 has a higher specific energy density than LiFePO4 used in practice: theoretical values of 700 and 580 W h/kg, respectively. However, its use is hampered by a number of disadvantages: reduced electronic and ionic conductivity, inferior stability of the structure in the charged form, and large changes in the volume during (de)lithiation. LiMnPO4 and LiMn0.95Ni0.05PO4 samples are synthesized by the solvothermal method and studied using X-ray powder diffraction, low-temperature nitrogen adsorption, scanning electron microscopy, and electrochemical methods. It is shown that a small degree of substitution of Mn for Ni (5 at %) leads to an increase in the capacity and Coulombic efficiency of LiMnPO4, a decrease in charge-transfer resistance, and an increase in Li+ diffusion coefficients.

锂和过渡金属磷酸盐是很有前途的锂离子电池正极材料。磷酸锰锂 LiMnPO4 比实际使用的磷酸铁锂具有更高的比能量密度:理论值分别为 700 瓦时/千克和 580 瓦时/千克。然而,它的使用受到一些缺点的阻碍:电子和离子导电性降低,带电结构的稳定性较差,以及在(脱)锂化过程中体积变化较大。我们采用溶热法合成了 LiMnPO4 和 LiMn0.95Ni0.05PO4 样品,并使用 X 射线粉末衍射、低温氮吸附、扫描电子显微镜和电化学方法对其进行了研究。结果表明,Mn 对 Ni 的少量替代(5%)会导致 LiMnPO4 的容量和库仑效率增加,电荷转移电阻减小,Li+ 扩散系数增大。
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引用次数: 0
Liposomes Containing Esters of the Natural Antioxidant Astaxanthin Modified with Pluronic F68 or DSPE-PEG 2000 含有经 Pluronic F68 或 DSPE-PEG 2000 修饰的天然抗氧化剂虾青素酯的脂质体
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601511
N. S. Marchenkova, K. E. Barkar, E. A. Kulikov, K. S. Plokhikh, N. Yu. Lotosh, A. A. Selishcheva

Liposomes containing a natural antioxidant, astaxanthin esters, are prepared by dispersing the lipid film and evaporating from chloroform with further ultrasonic treatment. To increase the stability of the astaxanthin esters, liposomes based on Lipoid S75 (2 mg/mL) are modified with pluronic F68 or PEGylated distearylphosphatidylethanolamine (DSPE-PEG 2000). As a result of optimization, the ratio of phospholipid and modifiers is selected for stable liposomes with 0.5 mg/mL astaxanthin esters. Liposomes with 0.5% pluronic F68 consists of two fractions with sizes of 110 ± 15 and 440 ± 15 nm, and liposomes with DSPE-PEG 2000 (2.5 mg/mL) have one fraction with an average hydrodynamic diameter of 255 ± 40 nm. The ζ potentials of the liposomes are –35 ± 15 and –60 ± 10 mV, respectively. When mononuclear blood cells are incubated with the developed liposomes for 24 h, the survival rate is found to be 84 ± 4%. It is shown that liposomes with astaxanthin esters of different compositions inactivate the ABTS cation radical 17–50% more effectively than liposomes without astaxanthin esters.

含有天然抗氧化剂虾青素酯的脂质体是通过分散脂膜和氯仿蒸发并进一步超声处理制备的。为了提高虾青素酯的稳定性,以 Lipoid S75(2 mg/mL)为基础的脂质体用 pluronic F68 或 PEG 化二硬脂酰磷脂酰乙醇胺(DSPE-PEG 2000)进行修饰。经过优化,磷脂和改性剂的比例被选定为 0.5 毫克/毫升虾青素酯的稳定脂质体。含 0.5% pluronic F68 的脂质体由两部分组成,大小分别为 110 ± 15 nm 和 440 ± 15 nm;含 DSPE-PEG 2000(2.5 mg/mL)的脂质体由一部分组成,平均流体力学直径为 255 ± 40 nm。脂质体的ζ电位分别为 -35 ± 15 和 -60 ± 10 mV。当单核血细胞与研制出的脂质体培养 24 小时后,发现存活率为 84 ± 4%。结果表明,与不含虾青素酯的脂质体相比,含有不同成分虾青素酯的脂质体灭活 ABTS 阳离子自由基的效果高出 17-50%。
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引用次数: 0
BC/PEDOT:PSS/Graphene Conductive Composite As the Receptor Element for a Bacterial Biosensor 作为细菌生物传感器受体元件的 BC/PEDOT:PSS/Graphene 导电复合材料
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601493
A. E. Kitova, Yu. V. Plekhanova, S. E. Tarasov, N. A. Klenova, A. N. Reshetilov

Тhe search for new materials with high conductivity and biocompatibility for use in biosensors is an important task. One promising material is bacterial cellulose (BC) due to its high surface area, high porosity, and biocompatibility. In this study, bacterial cellulose is modified with the PEDOT:PSS conductive gel and carbon nanomaterials to increase conductivity. Thermally expanded graphite/BC/PEDOT:PSS/graphene composition is used to immobilize Gluconobacter oxydans acetic-acid bacteria on the surface of a screen-printed carbon electrode. The effect of individual components of the composite on the catalytic activity of bacteria in the presence of 2,6-dichlorophenolindophenol redox mediator is studied. The addition of BC to the composition provides a higher stability of the electrode: the drop in signal within 35 days is 9%. A microbial biosensor based on TEG/PEDOT:PSS/Graphene/BC/G. oxydans composite show better sensitivity (36.4 µA mM–1 cm–2) and lower detection limit (0.005 mM) as well as the widest linear detection range (0.005–2 mM) compared to the other compositions. Thus, bacterial cellulose modified with conductive additives can be applied as a matrix for the immobilization of bacteria in microbial biosensors and microbial fuel cells.

寻找具有高导电性和生物兼容性的新材料用于生物传感器是一项重要任务。细菌纤维素(BC)因其高比表面积、高孔隙率和生物相容性而成为一种前景广阔的材料。在这项研究中,用 PEDOT:PSS 导电凝胶和碳纳米材料对细菌纤维素进行改性,以提高其导电性。热膨胀石墨/BC/PEDOT:PSS/石墨烯组合物用于在丝网印刷碳电极表面固定醋酸葡萄糖杆菌。研究了在 2,6-二氯苯酚-靛酚氧化还原介质存在下,复合材料中各组分对细菌催化活性的影响。在复合材料中添加 BC 可提高电极的稳定性:35 天内信号下降率为 9%。与其他成分相比,基于 TEG/PEDOT:PSS/Graphene/BC/G. oxydans 复合材料的微生物生物传感器具有更高的灵敏度(36.4 µA mM-1 cm-2)和更低的检测限(0.005 mM),以及最宽的线性检测范围(0.005-2 mM)。因此,用导电添加剂改性的细菌纤维素可用作微生物生物传感器和微生物燃料电池中固定细菌的基质。
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引用次数: 0
Improvement of the Bioavailability of Low-Solubility Drugs by Reprecipitation on Nanostructured Surfaces 通过在纳米结构表面再沉淀提高低溶解度药物的生物利用度
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167623601262
O. D. Smirnova, V. Yu. Musatova, I. V. Kalashnikova, S. V. Aleshin, S. A. Semenov, L. V. Kostryukova, G. E. Morozevich

Тhis work suggests ways to improve the bioavailability of low-solubility drugs by precipitation from solutions in universal solvents on nanostructured surfaces including nanoparticles (NPs) such as SiO2 and Fe3O4. The same effect is found on metal-polymer composites containing Co, Ni, and Fe obtained from unsaturated dicarboxylates. In both cases, this is achieved by increasing the total desorption surface. The examples of resveratrol and of the preparation of the sum of furocoumarins Ammifurin show an increase of the relative desorption ratio of drugs by two orders of magnitude from the surface of nanostructured CaCO3 particles into aqueous solutions. The results of MTT tests show the comparable effects of Ammifurin and of the used metal-polymer nanocomposites on HeLa cervical cancer cells and human HepG2 liver carcinoma, thereby making their combined use potentially possible. Thus, we propose a way to improve the bioavailability of a wide class of drugs, potentially applicable for all cases when the toxicity of the carrier NPs does not exceed the independent toxicity of the target substance. The possibility of the mutual enhancement of toxicity requires a separate study and is not considered here.

这项研究提出了通过从通用溶剂溶液中沉淀到纳米结构表面(包括二氧化硅和氧化铁等纳米粒子)来提高低溶解度药物生物利用度的方法。由不饱和二羧酸盐制成的含有 Co、Ni 和 Fe 的金属聚合物复合材料也具有同样的效果。在这两种情况下,都是通过增加总解吸表面来实现的。白藜芦醇和呋喃香豆素 Ammifurin 总和的制备实例表明,药物从纳米结构 CaCO3 颗粒表面进入水溶液的相对解吸率提高了两个数量级。MTT 测试结果表明,Ammifurin 和所使用的金属聚合物纳米复合材料对 HeLa 宫颈癌细胞和人类 HepG2 肝癌的作用相当,因此有可能将它们结合使用。因此,我们提出了一种提高各类药物生物利用度的方法,当载体 NPs 的毒性不超过目标物质的独立毒性时,这种方法可能适用于所有情况。相互增强毒性的可能性需要单独研究,在此不予考虑。
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引用次数: 0
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Nanotechnologies in Russia
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