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Application of Gold Nanorods in Combination with Surface-Enhanced Raman Spectroscopy for Immunochromatographic Determination of Ochratoxin A 将金纳米棒与表面增强拉曼光谱结合应用于赭曲霉毒素 A 的免疫层析测定
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167624600391
K. V. Serebrennikova, L. V. Barshevskaya, A. V. Zherdev, B. B. Dzantiev

The aim of the study was to increase the sensitivity of immunochromatographic assay (ICA), achieved using gold nanorods modified with 5,5'-dithiobis-(2-nitrobenzoic acid). The resulting nanomarker makes it possible to quantify the target analyte using colorimetry and surface-enhanced Raman spectroscopy (SERS). One of the widespread mycotoxins, ochratoxin A (OTA), was chosen as the object of study. After functionalization of gold nanorods with antispecies antibodies, the SERS-active tag was used to detect immune complexes formed in the analytical zone as a result of the competitive interaction between free OTA and the hapten-protein conjugate for the binding sites of specific antibodies. After immunochromatographic assay, SERS intensity of 5,5'-dithiobis-(2-nitrobenzoic acid) was measured. Under optimized conditions, the detection limit of OTA in the colorimetric detection mode was 1.7 ng/mL, and when recording ICA results using SERS, it decreased to 33 pg/mL.

摘要 该研究的目的是利用用 5,5'-二硫双(2-硝基苯甲酸)修饰的金纳米棒提高免疫层析(ICA)的灵敏度。由此产生的纳米标记物可以利用比色法和表面增强拉曼光谱(SERS)对目标分析物进行定量。赭曲霉毒素 A(OTA)是一种广泛存在的霉菌毒素,被选为研究对象。在用抗物种抗体对金纳米棒进行功能化之后,SERS 活性标签被用来检测分析区中由于游离 OTA 与合蛋白共轭物对特异性抗体结合位点的竞争性作用而形成的免疫复合物。免疫层析检测后,测量 5,5'-二硫双(2-硝基苯甲酸)的 SERS 强度。在优化条件下,比色检测模式下 OTA 的检测限为 1.7 纳克/毫升,而使用 SERS 记录 ICA 结果时,检测限降至 33 皮克/毫升。
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引用次数: 0
X-Ray- and Synchrotron-Radiation Study of the Defect Structure of Epitaxial ZnO Films Grown by Magnetron Deposition on Al2O3 and LaMgAl11O19 Substrates with (0001) Orientation 通过磁控沉积法在具有 (0001) 取向的 Al2O3 和 LaMgAl11O19 基质上生长的外延氧化锌薄膜的缺陷结构的 X 射线和同步辐射研究
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167623601365
V. A. Zhernova, Yu. A. Volkovsky, M. S. Folomeshkin, A. Yu. Seregin, P. A. Prosekov, A. E. Muslimov, A. V. Butashin, A. M. Ismailov, Yu. V. Grigoriev, Yu. V. Pisarevsky, V. M. Kanevsky, A. E. Blagov, M. V. Kovalchuk

The results of studying the structural features of samples of zinc-oxide films obtained by magnetron deposition on chips of lanthanum-magnesium hexaaluminate and the surface of sapphire substrates with a gold buffer layer are presented. Analysis of the structure and morphology of the films is carried out using a set of methods, including high-resolution X-ray diffractometry, the method of constructing pole figures, and transmission electron microscopy. It is shown that when using cleavages of lanthanum-magnesium hexaaluminate, an epitaxial ZnO film is formed without signs of growth rotating domains. The use of a gold buffer layer during growth on sapphire substrates improves the crystalline quality of ZnO films, but does not completely suppress domain growth.

摘要 介绍了在六铝酸镧镁芯片和带金缓冲层的蓝宝石衬底表面上通过磁控沉积获得的氧化锌薄膜样品结构特征的研究结果。分析薄膜的结构和形态采用了一系列方法,包括高分辨率 X 射线衍射测量法、极坐标法和透射电子显微镜。结果表明,在使用六铝酸镧镁的裂隙时,形成的氧化锌外延薄膜没有生长旋转畴的迹象。在蓝宝石衬底上生长过程中使用金缓冲层可提高氧化锌薄膜的结晶质量,但不能完全抑制畴生长。
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引用次数: 0
Anisotropy of Nitrogen Vacancy Diffusion in AlN with a Wurtzite Structure 具有沃特兹结构的氮化铝中氮空位扩散的各向异性
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167624600317
M. A Danilyak, I. V. Belov, V. G. Valeev

The diffusion tensor of nitrogen vacancies in crystalline aluminum nitride with a wurtzite structure is calculated, and the nature of its dependence on the concentration of vacancies and the temperature of the system is studied. The results obtained are necessary for the development of a closed hydrodynamic description of the processes of formation and evolution of vacancy filaments in nitride memristive structures with resistive switching.

摘要 计算了晶状氮化铝中的氮空位扩散张量,并研究了其与空位浓度和系统温度的关系。所获得的结果对于对具有电阻开关功能的氮化忆阻结构中空位丝的形成和演变过程进行封闭流体力学描述是必要的。
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引用次数: 0
Silver Crown Particles with Multiwalled Carbon Nanotubes Skeletons 具有多壁碳纳米管骨架的银冠颗粒
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167624600238
V. A. Vagapov, O. A. Vasilenko, A. V. Golubev, O. V. Demicheva, N. A. Karapuzova

The types of metal-composite particles produced as a result of the chemical silvering of DEALTOM multiwalled carbon nanotubes (MWCNTs) dispersed in a solution are studied. A silver polycrystalline coating of the surface of MWCNTs is obtained by the adsorption method. A new property is discovered, namely the fusion of silver-plated nanotubes obtained in this way into crown particles and the ability to agglomerate into various macrostructures. Studying the Dealtom metallized MWCNT structure by means of the scanning electron microscope reveals the following types of metallization in the samples: lamellar silver crystals (0.1–3 μm) on few and single active centers of the MWCNT surface; a silver polycrystalline layer on the surface of the MWCNTs; a polycrystalline coating of each MWCNT in a coil of nanotubes with subsequent fusion into a single silver crown particle (1–10 μm); hybrid particles, which are lamellar crystals of silver on the polycrystalline silver surface of the crown particle; the fusion of two or more crown particles into a 1D chain and 2D carpet macrostructures. The synthesized hybrid particles with nanobranched pointed morphology are promising for use in surface-enhanced Raman scattering (SERS) spectroscopy for determining ultra-low concentrations of substances as well as for analyzing biological objects.

摘要 研究了对分散在溶液中的 DEALTOM 多壁碳纳米管(MWCNTs)进行化学银化而产生的金属复合颗粒的类型。通过吸附法在 MWCNT 表面获得了多晶银涂层。研究发现了一种新特性,即通过这种方法获得的镀银纳米管可融合成冠状颗粒,并能聚结成各种宏观结构。通过扫描电子显微镜研究 Dealtom 金属化 MWCNT 结构,可以发现样品中的金属化类型如下:片状银晶体(0.1-3 μm);MWCNT 表面的银多晶层;纳米管线圈中每个 MWCNT 的多晶涂层,随后融合成单个银冠颗粒(1-10 μm);混合颗粒,即在冠颗粒的多晶银表面形成片状银晶体;两个或多个冠颗粒融合成 1D 链和 2D 地毯状宏观结构。合成的杂化颗粒具有纳米带状尖头形态,有望用于表面增强拉曼散射(SERS)光谱,以确定超低浓度的物质以及分析生物物体。
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引用次数: 0
Changes in the Fine Structure of Natural Graphite in the Process of Mechanical Dispersion 天然石墨精细结构在机械分散过程中的变化
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167624600329
A. G. Fazlitdinova, V. A. Tyumentsev

Changes in the fine structure of natural graphite ground in a planetary mill in an atmosphere of air and Ar + 10% CH4 are studied by X-ray diffraction. The profiles of the experimentally observed asymmetric maxima of 002 graphite are decomposed into the minimum number of symmetric components described by the Pearson VII function using the Origin program (determination coefficient R2 is 0.985–0.999). The asymmetric peaks 002 can be represented as a superposition of the minimum number of components of symmetrical expansion. In this case, the calculated values of the interplanar spacings (d002) of the decomposition components are quite close to the values of d002 of the metastable states (phases) given earlier in publications. It is shown that the process of dispersion and structural transformations develops along the path of the successive formation of components with an increased interplanar spacing d002 in the range from ∼3.36 to ∼3.55/3.68 Å. Dispersion is not limited to a reduction in the particle size of graphite. Replacing the air atmosphere with Ar + 10%CH4 has the most significant effect on graphite dispersion in the first ~40 min.

摘要 通过 X 射线衍射研究了在空气和 Ar + 10% CH4 的气氛中用行星式研磨机研磨的天然石墨精细结构的变化。使用 Origin 程序(确定系数 R2 为 0.985-0.999)将实验观察到的石墨 002 非对称最大值的剖面分解为皮尔逊 VII 函数所描述的最小数量的对称成分。非对称峰 002 可以表示为对称膨胀最小分量的叠加。在这种情况下,分解分量的平面间距(d002)的计算值与早先出版物中给出的陨石态(相)的 d002 值非常接近。研究表明,分散和结构转变过程是沿着连续形成成分的路径发展的,成分的平面间距 d002 在 ∼3.36 Å 到 ∼3.55/3.68 Å 范围内增大。在最初的 ~40 分钟内,用 Ar + 10%CH4 取代空气对石墨分散的影响最为显著。
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引用次数: 0
Three Types of the Two-Phase Surface Tension of Molecules in Mesoporous Systems and Methods for Their Calculation 介孔体系中分子两相表面张力的三种类型及其计算方法
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S263516762460041X
Yu. K. Tovbin, E. S. Zaitseva

At temperatures T < Tc(H) (where Tc(H) is the critical temperature and H is the characteristic pore size), in all mesoporous systems sorbed adsorbate molecules are separated into two coexisting phases “vapor in a pore” and “liquid in a pore”. The conditions for such adsorbate separation depend on the pore width and adsorbent–adsorbate interaction energies. The distribution of an adsorbate over the pore volume in different materials plays an important role in the processes of substance transfer and the establishment of an equilibrium state in them. The separation of molecules is accompanied by the formation of menisci at the vapor–liquid interface. They largely determine the overall resistance to the process of mass transfer through porous materials. The most advanced results on the description of vapor–liquid interfaces are obtained on the basis of the so-called molecular lattice-gas model, which makes it possible to calculate the molecular distributions in heterogeneously distributed models of transition regions with equal accuracy. Nondeformable pore walls create an external field that affects the molecular distribution and forms adsorption films due to the adsorbate-adsorbent interaction potential. The surface tension of the discussed menisci, as well as at the boundaries between the vapor or liquid adsorbate and solid walls, is calculated from the excess free energy of the interface (according to Gibbs). The state of the coexisting phases “vapor in a pore” and “liquid in a pore” must satisfy the equality of chemical potentials, excluding the appearance of metastable states. Methods for calculating three types of two-phase surface tensions in a three-aggregate system and a method for localizing areas of three-phase contact, as well as a microscopic description of the molecular distributions and properties of these areas are outlined. The approach is demonstrated using the example of slit-like pores with smooth and rough walls, as well as cylindrical pores and their junctions between pores of different radii. The size effects of the contact angle are studied as a function of the geometry of the pore cross section and the potential of the pore walls. The results obtained are ahead of the level of existing published works.

摘要在温度 T <Tc(H)(其中 Tc(H) 为临界温度,H 为特征孔径)下,所有介孔系统中吸附的吸附剂分子都会分离成 "孔中蒸气 "和 "孔中液体 "两种共存相。这种吸附分离的条件取决于孔隙宽度和吸附剂与吸附剂之间的相互作用能。在不同材料的孔隙中,吸附剂的分布在物质转移和建立平衡状态的过程中起着重要作用。分子的分离伴随着汽液界面半月板的形成。它们在很大程度上决定了多孔材料传质过程的总体阻力。关于汽液界面描述的最先进结果是在所谓的分子晶格-气体模型基础上获得的,该模型使得在过渡区域的异质分布模型中以同等精度计算分子分布成为可能。不可变形的孔壁会产生一个外部场,该场会影响分子分布,并由于吸附剂与吸附剂之间的相互作用势形成吸附膜。所讨论的孔壁以及蒸气或液体吸附剂与固体孔壁之间边界的表面张力是通过界面的过剩自由能计算得出的(根据吉布斯原理)。孔隙中的蒸气 "和 "孔隙中的液体 "共存相的状态必须满足化学势相等的条件,不包括出现蜕变态。本文概述了三聚体系中三种两相表面张力的计算方法、三相接触区域的定位方法以及这些区域的分子分布和性质的微观描述。该方法以具有光滑和粗糙孔壁的狭缝状孔隙、圆柱形孔隙及其不同半径孔隙之间的交界处为例进行了演示。研究了接触角的大小效应与孔隙横截面几何形状和孔壁电位的函数关系。所获得的结果领先于现有已发表的研究成果。
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引用次数: 0
Analysis of the Reducing Activity of Strains of the Genus Shewanella Isolated from Various Natural Sources Using the Example of the Biosynthesis of Silver Nanoparticles 以银纳米粒子的生物合成为例,分析从各种天然资源中分离出来的雪旺菌属菌株的还原活性
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167623601420
T. A. Voeikova, O. A. Zhuravliova, T. L. Babich, S. N. Malakhov, T. D. Patsaev, A. L. Vasiliev, E. I. Kozhukhova, P. A. Zhdanov, A. Yu. Vlasova, A. I. Kilochek, V. G. Debabov

For the first time, a comparative analysis of 8 strains of the genus Shewanella isolated from various natural sources is carried out according to the level of the reducing activity of Ag+ to silver-containing nanoparticles (NPs). The characteristics of biogenic NPs in terms of shape, size, crystal-lattice parameters, hydrodynamic diameter, ζ potential, and optical characteristics are obtained using scanning transmission electron microscopy, dynamic light scattering, spectrophotometry, atomic emission spectroscopy, and assessment of the biocidal activity against various types of microorganisms, including the studied strains of the genus Shewanella. It is found that the shape of the NPs is close to spherical, the sizes vary from 2 to 30 nm, the samples are polydisperse colloidal systems. Analysis of crystal lattices of the NPs confirms the presence of AgNPs, as well as Ag2O2NPs and Ag3O4NPs in some samples. The results of atomic emission spectroscopy on the quantitative analysis of the content of Ag in the nanomaterial samples are obtained, on the basis of which strains with a high ability to form a Ag-containing nanomaterial are identified. The high sensitivity of gram-positive bacteria to AgNPs is established. Different levels of resistance of 8 strains of the genus Shewanella to the action of biogenic AgNPs are demonstrated. The results indicate the metabolic diversity of strains of the genus Shewanella isolated from various natural sources. The analysis of strains of the genus Shewanella according to the level of the reducing activity is relevant for the development of an effective technology for the “green” synthesis of biogenic NPs.

摘要 首次根据Ag+对含银纳米粒子(NPs)还原活性的高低,对从各种天然资源中分离的8株卵球菌(Shewanella)进行了比较分析。利用扫描透射电子显微镜、动态光散射、分光光度法、原子发射光谱法获得了生物纳米粒子在形状、大小、晶格参数、流体力学直径、ζ电位和光学特性方面的特征,并评估了对各类微生物(包括所研究的雪旺菌属菌株)的杀菌活性。研究发现,NPs 的形状接近球形,大小从 2 纳米到 30 纳米不等,样品是多分散胶体系统。对 NPs 晶格的分析证实了 AgNPs 以及 Ag2O2NPs 和 Ag3O4NPs 在某些样品中的存在。原子发射光谱对纳米材料样品中的Ag含量进行了定量分析,在此基础上确定了形成含Ag纳米材料能力强的菌株。确定了革兰氏阳性细菌对 AgNPs 的高度敏感性。结果表明,雪旺氏菌属的 8 株菌株对生物源 AgNPs 的作用具有不同程度的抗性。研究结果表明,从各种天然来源分离出来的雪旺菌属菌株具有代谢多样性。根据还原活性水平对卵球菌属菌株进行分析,对于开发 "绿色 "合成生物纳米粒子的有效技术具有重要意义。
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引用次数: 0
Ferrocene-Containing Polymethacrylates: Synthesis, Molecular Characteristics, and Its Nanoparticles 含二茂铁的聚甲基丙烯酸酯:合成、分子特征及其纳米颗粒
IF 0.8 Q3 Engineering Pub Date : 2024-08-06 DOI: 10.1134/S2635167624600469
I. Yu. Perevyazko, P. A. Fetin, I. M. Zorin, A. A. Lezov, A. A. Lezova, N. G. Mikusheva, K. V. Deriabin, R. M. Islamova, N. V. Tsvetkov

In this work, a series of samples of a homopolymer of polyferrocenoylethylmethacrylate containing ferrocene groups in side chains is synthesized for the first time using the RAFT polymerization method and comprehensively studied. A homologous series of polymers differing in molar mass is obtained in a range sufficient for conformational analysis. The main hydrodynamic characteristics of polymers (intrinsic viscosity, sedimentation, and translational diffusion coefficients) are studied, and the most probable conformation of polymers in a solution as well as the main conformational parameters (thermodynamic rigidity and polymer-chain diameter) are determined. Also, suspensions of nanoparticles are prepared on the basis of the studied polymers by the method of nanoprecipitation. The sizes of the obtained particles are analyzed both on substrates and in suspensions.

摘要 在这项工作中,首次使用 RAFT 聚合方法合成了一系列侧链中含有二茂铁基团的聚二茂铁甲酰乙基甲基丙烯酸酯均聚物样品,并对其进行了全面研究。获得了一系列摩尔质量不同的同源聚合物,其范围足以进行构象分析。研究了聚合物的主要流体力学特性(固有粘度、沉降和平移扩散系数),确定了聚合物在溶液中的最可能构象以及主要构象参数(热力学刚性和聚合物链直径)。此外,还以所研究的聚合物为基础,通过纳米沉淀法制备了纳米颗粒悬浮液。对基底和悬浮液中获得的颗粒大小进行了分析。
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引用次数: 0
Application of Nickel Foam As a Porous Transport Layer in a Anion Exchange Membrane Water Electrolyzer 镍泡沫作为多孔传输层在阴离子交换膜水电解槽中的应用
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167624600159
I. V. Pushkareva, A. S. Pushkarev, M. A. Solovyev, S. I. Butrim, V. N. Kuleshov, S. V. Kurochkin, N. V. Kuleshov, V. N. Fateev

Тhe efficiency and the performance of membrane electrode assemblies (MEAs) of the anion exchange membrane (AEM) water electrolyzer is determined to a significant degree by the properties of the materials used as porous transport layers (PTLs). Due to the high surface roughness, porosity, and pore size, the direct use of Ni foam as an electrode material is difficult, and its preliminary compression is required, which irreversibly affects the electrode structure. In the presented work, the effect of Ni foam compression on the structure of an electrode based on it, as well as on the AEM water electrolyzer MEA is considered, including the distribution of voltage losses. The effect of the compression degree on the Ni-foam electrode structure and the performance of the AEM water electrolyzer MEA is considered. The optimal electrode compression provides a significant decrease in the loss of microporous layer particles and catalyst layer nanoparticles in deep surface voids of the PTL, and the development of an interface between the nanostructured catalyst layer and the electrode.

阴离子交换膜(AEM)水电解槽膜电极组件(MEA)的效率和性能在很大程度上取决于用作多孔传输层(PTL)的材料的特性。由于泡沫镍具有较高的表面粗糙度、孔隙率和孔径,因此很难直接用作电极材料,而且需要对其进行初步压缩,这对电极结构造成了不可逆的影响。在本研究中,考虑了压缩泡沫镍对以其为基础的电极结构以及 AEM 水电解槽 MEA 的影响,包括电压损失的分布。研究还考虑了压缩程度对镍泡沫电极结构和 AEM 水电解槽 MEA 性能的影响。最佳电极压缩度可显著减少 PTL 深表面空隙中微孔层颗粒和催化剂层纳米颗粒的损失,并在纳米结构催化剂层和电极之间形成界面。
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引用次数: 0
On the Electrochemical Synthesis of Nanodispersed, Submicrodispersed, and Microdispersed Powders of Molybdenum and Tungsten Carbides in Chloride-Oxide Melts 在氯氧化物熔体中电化学合成纳米分散、亚微分散和微分散的钼和碳化钨粉末
IF 0.8 Q3 Engineering Pub Date : 2024-03-23 DOI: 10.1134/S2635167624600160
H. B. Kushkhov, M. N. Ligidova, R. Kh. Karatsukova, A. A. Khotov, Zh. Z. Ali

In the work, using the methods of cyclic voltammetry and open-circuit chronopotentiometry, and galvanostatic and potentiostatic electrolysis, the processes of the joint electroreduction of molybdate (tungstate) ions with carbonate ions against the background of a melt of potassium chloride at 1023–1173 K are studied. The possibility of the joint electrolysis of molybdenum (tungsten) and carbon in a potassium-chloride melt and the implementation on their basis of the electrochemical synthesis of molybdenum and tungsten carbides in the form of nanodispersed, submicrodispersed, and microdispersed powders. Samples of molybdenum and tungsten carbides are synthesized and characterized by X-ray phase analysis, laser particle-size analysis, and scanning electron microscopy.

该研究采用循环伏安法、开路计时电位法、静电电解法和静电电位法,研究了在 1023-1173 K 的氯化钾熔体背景下钼酸根(钨酸盐)离子与碳酸根离子的联合电还原过程。在氯化钾熔体中联合电解钼(钨)和碳的可能性,以及在此基础上以纳米分散、亚微分散和微分散粉末形式电化学合成钼和碳化钨的实施情况。合成的钼和碳化钨样品通过 X 射线相分析、激光粒度分析和扫描电子显微镜进行表征。
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引用次数: 0
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Nanotechnologies in Russia
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