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Dependence of the Structure of Segregations on the Excess Volume of Intergranular Boundaries 偏析结构与晶间界过剩体积的关系
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x23601233
S. L. Lomaev, L. S. Vasil’ev

Abstract

The work is devoted to the analysis of the nonlinear effects resulting from the influence of excess volumes of intergranular boundaries on the structure of segregations of impurity atoms in polycrystals. It is shown that the adsorption isotherm can describe the nonuniformities in the distribution of impurity atoms in the plane of an intergranular boundary. This suggests the existence of adsorption sites at the internal boundaries of polycrystals. It is proven that an excess volume of intergranular boundaries is the main parameter determining the magnitude of impurity segregations at the boundaries.

摘要 该研究致力于分析晶间边界过大体积对多晶体中杂质原子偏析结构的影响所产生的非线性效应。研究表明,吸附等温线可以描述杂质原子在晶间界平面上分布的不均匀性。这表明在多晶体的内部边界存在吸附点。事实证明,晶间边界的过剩体积是决定边界杂质偏析程度的主要参数。
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引用次数: 0
Enzymatic Sol-Gel Transition in Milk 牛奶中的酶溶胶-凝胶转变
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x23601385
I. T. Smykov, D. S. Myagkonosov

Abstract

The objective of this study is to enhance the comprehension of the mechanism of enzymatic gelation in milk by investigating statistically significant changes in milk viscosity and carrying out corresponding electron microscopic studies of the process of structure formation at the enzymatic stage of coagulation using various enzyme preparations. Employing a non-destructive method (Hot-Wire) to monitor viscosity, we were able to confirm a decrease in viscosity during the middle of this stage and identify a previously undescribed peak in viscosity change at the end of the enzymatic stage. By conducting parallel studies utilizing transmission electron microscopy and various methods of specimen preparation, it was possible to discover that a hierarchical transformation process in the protein component of milk started at the end of the enzymatic stage of gelation in milk. This process is triggered by a cooperative conformational transition in casein micelle clusters, which leads to a series of increasingly energy-intensive reactions resulting in the transformation of loosely bound micelle clusters into denser aggregates. The final structure of the milk gel primarily consists of the previously formed individual micelle aggregates. It was noted that no changes in the microstructure of the milk gel were observed during the enzymatic stage of gelation when milk-clotting enzymes (MCEs) of animal, plant, and microbial (GMO) origins were used. Furthermore, investigations into the molecular weight distribution of soluble protein substances in samples generated with different types of MCEs revealed that the enzyme derived from the fungi of Rhizomucor miehei had a greater proteolytic effect on milk proteins compared to other variants of MCEs.

摘要 本研究的目的是通过对牛奶粘度的显著变化进行统计调查,并利用各种酶制剂对凝结酶解阶段的结构形成过程进行相应的电子显微镜研究,从而加深对牛奶酶解凝胶机理的理解。通过采用非破坏性方法(热丝)监测粘度,我们证实了在该阶段中期粘度的下降,并确定了在酶解阶段末期粘度变化的一个以前未曾描述过的峰值。通过利用透射电子显微镜和各种试样制备方法进行并行研究,我们发现牛奶中的蛋白质成分在牛奶凝胶酶解阶段末期开始了分层转变过程。这一过程是由酪蛋白胶束簇的协同构象转变引发的,它导致一系列能量消耗越来越大的反应,使松散的胶束簇转变为更致密的聚集体。牛奶凝胶的最终结构主要由之前形成的单个胶束聚集体组成。我们注意到,在凝胶化的酶解阶段,当使用动物、植物和微生物(转基因生物)来源的牛奶凝固酶(MCE)时,没有观察到牛奶凝胶的微观结构发生变化。此外,对使用不同类型的牛奶凝固酶生成的样品中可溶性蛋白质物质的分子量分布进行的研究表明,与其他变体的牛奶凝固酶相比,从根瘤菌中提取的牛奶凝固酶对牛奶蛋白质的蛋白水解作用更大。
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引用次数: 0
Effect of Electrostatic Interactions in Wormlike Micelles of Surfactants Based on Betaine and Charged Tertiary Amine with the Same Hydrophobic Groups 基于甜菜碱的表面活性剂和具有相同疏水基团的带电荷叔胺的蠕虫状胶束中的静电相互作用效应
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x23601373
W. Hao, V. S. Molchanov, Yu. M. Chesnokov, P. R. Podlesnyi, O. E. Philippova

Abstract

The viscoelastic properties and structure of solutions of mixed wormlike micelles based on a zwitterionic surfactant, oleylamidopropyldimethylcarboxybetaine (OAPB), and positively charged oleylamidopropyldimethylamine (OAPA) have been studied at different ratios between the components. At a small fraction of the cationic surfactant, OAPA, the solution exhibits viscoelastic properties characteristic of semidiluted solutions of entangled wormlike micelles, the presence of which has been confirmed by cryogenic electron microscopy data. It has been found that, as the molar fraction of the charged surfactant increases to 0.1, the viscosity and relaxation time of the solutions decrease by a factor of three, and the values of the storage modulus remain unchanged at short stress action times. The studied surfactants have a similar structure; therefore, when replacing zwitterionic OAPB molecules by positively charged OAPA molecules, the main factor of variations in the properties and structure is the enhancement of the electrostatic repulsion on the micelle surface. It has been shown that this factor leads to a decrease in the average length of micelles and an increase in their number, which have a weak effect on the rheological properties of the system as long as the length of the micelles is larger than the length of the subchains in the network. With an increase in the molar fraction of OAPA from 0.1 to 0.5, the viscosity and relaxation time drop drastically by several orders of magnitude and the viscoelastic response of the solution is lost; i.e., the network is destroyed. This transition from a semidilute solution to a dilute one is explained by a decrease in the length of the wormlike micelles and the formation of spherical ones. Cryogenic electron microscopy images have confirmed the formation of a mixture of long and short wormlike micelles with spherical micelles at an OAPA molar fraction of 0.5.

摘要 研究了基于油酰胺丙基二甲基羧基甜菜碱(OAPB)和带正电荷的油酰胺丙基二甲基胺(OAPA)的齐微阳离子表面活性剂混合虫胶团溶液在不同组分比例下的粘弹性能和结构。当阳离子表面活性剂 OAPA 的含量较低时,溶液就会表现出缠结蚯蚓状胶束半稀释溶液所特有的粘弹性,低温电子显微镜数据证实了这种现象的存在。研究发现,当带电表面活性剂的摩尔分数增加到 0.1 时,溶液的粘度和松弛时间减少了三倍,而在短应力作用时间内,存储模量的值保持不变。所研究的表面活性剂具有相似的结构;因此,当带正电荷的 OAPA 分子取代带偶离子的 OAPB 分子时,性质和结构变化的主要因素是胶束表面静电斥力的增强。研究表明,只要胶束的长度大于网络中子链的长度,这一因素就会导致胶束平均长度的减少和数量的增加,而这对体系流变特性的影响很小。随着 OAPA 摩尔分数从 0.1 增加到 0.5,粘度和弛豫时间急剧下降了几个数量级,溶液失去了粘弹性响应,即网络被破坏。这种从半稀释溶液到稀释溶液的转变可以用蠕虫状胶束长度的减少和球形胶束的形成来解释。低温电子显微镜图像证实,在 OAPA 摩尔分数为 0.5 时,形成了长短蚯蚓状胶束与球形胶束的混合物。
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引用次数: 0
Sorption of Radium-226 on Few-Layer Graphene Synthesized under Conditions of Self-Propagating High-Temperature Synthesis 自蔓延高温合成条件下合成的少层石墨烯对镭-226 的吸附作用
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x23601348
A. A. Vozniakovskii, A. P. Voznyakovskii, S. V. Kidalov, A. P. Karmanov, N. G. Rachkova, N. D. Podlozhnyuk

Abstract

Human industrial activity is accompanied by the formation of vast volumes of water contaminated with radionuclides, including radium-226, which create serious danger to people. Graphene nanostructures are among the most promising materials for purifying water from radionuclides. This work has been devoted to investigating the efficiency of few-layer graphene synthesized under conditions of self-propagating high-temperature synthesis from cellulose and wastes of the woodworking industry (technical lignin, tree bark) for purifying water from radium-226. The key advantage of the method chosen for synthesis of few-layer graphene is the possibility to synthesize large volumes of the material at an acceptable cost, which is extremely important for industrial applications. It has been found that the synthesized samples of few-layer graphene can efficiently purify water from radium-226 (the degree of sorption is higher than 99%). It has also been shown that the degree of desorption upon repeated washing with water does not exceed 0.5%.

摘要 伴随着人类的工业活动,形成了大量受放射性核素(包括镭-226)污染的水,对人类造成严重危害。石墨烯纳米结构是最有希望净化水中放射性核素的材料之一。这项工作致力于研究在纤维素和木材加工业废料(工业木质素、树皮)自发热高温合成条件下合成的几层石墨烯在净化水中镭-226 的效率。选择这种方法合成少层石墨烯的主要优点是可以以可接受的成本合成大量材料,这对工业应用极为重要。研究发现,合成的几层石墨烯样品可以有效地净化水中的镭-226(吸附率高于 99%)。研究还表明,经水反复洗涤后,解吸程度不超过 0.5%。
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引用次数: 0
Features of Polyimide Films with Molecular Imprints of Erythrosine and Indigocarmine 具有赤藓红和靛红分子印迹的聚酰亚胺薄膜的特征
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x24600088
S. A. Khalzova, A. N. Zyablov, A. Yu. Vybornyi

Abstract

Polyimide films with molecular imprints of erythrosine and indigocarmine have been obtained. The structure and morphology of the film surfaces have been studied by scanning probe microscopy and IR spectroscopy. It has been found that the surface roughness of molecularly imprinted polymers (MIPs) increases, while the relief height amounts to 3–4 nm. The removal of template molecules leads to a redistribution of pores over sizes in the polymers with molecular imprints. The adsorption of dyes by MIP films has been carried out under static conditions. The degrees of extraction and the imprinting factors have been calculated for polymers with molecular imprints of the dyes. The high values of these parameters indicate the selectivity of MIPs to the target template molecules.

摘要 获得了带有赤藓红和靛红分子印记的聚酰亚胺薄膜。通过扫描探针显微镜和红外光谱对薄膜表面的结构和形态进行了研究。研究发现,分子印迹聚合物(MIPs)的表面粗糙度增加,浮雕高度达到 3-4 纳米。去除模板分子会导致带有分子印迹的聚合物中孔隙大小的重新分布。MIP 薄膜对染料的吸附是在静态条件下进行的。计算了带有染料分子印记的聚合物的萃取度和印记因子。这些参数的高值表明了 MIP 对目标模板分子的选择性。
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引用次数: 0
Effects of pH and Indifferent Electrolyte Concentration on the Aggregate Stability of Detonation Nanodiamond Hydrosol pH 值和不同电解质浓度对引爆纳米金刚石水溶液聚集稳定性的影响
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-05-07 DOI: 10.1134/s1061933x23601282
A. V. Volkova, A. A. Beloborodov, V. A. Vodolazhskii, E. V. Golikova, L. E. Ermakova

Abstract

Coagulation of polydisperse detonation nanodiamond (DND) hydrosol containing primary aggregates with a prevailing average size in a range of 20–200 nm has been studied experimentally and theoretically within the framework of the classical and extended DLVO theory as depending on the concentrations of an indifferent electrolyte (NaCl) and potential-determining ions (pH). It has been shown that the surface of DND particles is charged due to the ionization of ionogenic amphoteric hydroxyl and acidic carboxyl groups located on it. The isoelectric point of the detonation nanodiamond particles has been found to correspond to pH 7.5. It has been revealed that the main stabilizing factor of the DND hydrosol is electrostatic. It has been shown that the stability and coagulation of the sol can be described within the framework of the extended DLVO theory using the effective Hamaker constant for primary porous aggregates and taking into account the initial polydispersity of the DND particles.

摘要 在经典和扩展 DLVO 理论的框架内,对多分散起爆纳米金刚石(DND)水溶液的凝结情况进行了实验和理论研究,该水溶液含有平均粒径在 20-200 纳米范围内的原生聚集体,其凝结情况取决于冷漠电解质(氯化钠)和电位决定离子(pH 值)的浓度。研究表明,由于位于 DND 颗粒表面的离子两性羟基和酸性羧基的电离作用,DND 颗粒表面带电。研究发现,起爆纳米金刚石颗粒的等电点相当于 pH 值 7.5。研究表明,DND 水溶液的主要稳定因素是静电。研究表明,溶胶的稳定性和凝结可以在扩展的 DLVO 理论框架内使用原生多孔聚集体的有效 Hamaker 常数进行描述,并考虑到 DND 颗粒的初始多分散性。
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引用次数: 0
Thermal Ice Melting Performance of Femtosecond Laser Metal Micro-Nano-Structured Surface 飞秒激光金属微纳结构表面的热融冰性能
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-04-10 DOI: 10.1134/s1061933x23601166
Ziyuan Liu, Qing Ma, Tingsong Zhang, Yujia Dai

Abstract

Improving thermal ice melting efficiency is very important in the practical application of anti-icing surfaces. This work investigated the thermal ice melting performance of micro-nano-structured surfaces fabricated by femtosecond laser. To the best of our knowledge, we found that the micro-nano-structured surfaces significantly improve the ice melting time for the first time. The shortest melting time was on the porous micro-nano-structured surface, about one third of the original surface. Moreover, it was proven that the accelerated ice melting surface had good durability. The research in this paper showed that the micro-nano-structured surfaces are very suitable for the surface that needs to be heated to melt ice, providing essential guidance for the design of the anti-icing surface.

摘要提高热融冰效率对于防冰表面的实际应用非常重要。这项工作研究了利用飞秒激光制造的微纳米结构表面的热融冰性能。据我们所知,我们首次发现微纳结构表面显著提高了融冰时间。多孔微纳结构表面的融冰时间最短,约为原表面的三分之一。此外,还证明了加速融冰表面具有良好的耐久性。本文的研究表明,微纳结构表面非常适用于需要加热融冰的表面,为防冰表面的设计提供了重要指导。
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引用次数: 0
Development of a New Biocompatible Colloid System to Improve the Solubility of Celecoxib 开发新型生物相容性胶体系统以提高塞来昔布的溶解度
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-04-10 DOI: 10.1134/s1061933x23601270
Alireza Salabat, Nesa Ghorbani

Abstract

In this research work, a new biocompatible microemulsion containing castor oil has been formulated to increase the solubility of celecoxib, as a well-known anti-inflammatory drug. In this formulation castor oil has also anti-inflammatory properties. The proposed oil-in-water microemulsion composed of Tween 80 as surfactant, isobutanol as co-surfactant, and castor oil as the oil phase. In the first step, the phase diagrams of the proposed colloid systems with surfactant to co-surfactant mass ratios of 4 : 1 and 2 : 1 were prepared at ambient temperature. Then, using the obtained phase diagrams, the appropriate formulations were selected by combining different percentages of water, oil, surfactant and co-surfactant in the microemulsion region. Some of physico-chemical properties, such as electrical conductivity, density, refractive index, surface tension and particle size of the selected microemulsion formulations have been determined at 298 K. After that, the solubility of celecoxib in the selected formulations was determined and compared with other reported microemulsion formulations. Interesting results from this section indicated that the solubility of celecoxib significantly increased compared to pure water and the previous proposed formulations. The results of this study can be used to provide suitable formulations based on the biocompatible microemulsions for celecoxib in pharmaceutical industry.

摘要 在这项研究工作中,配制了一种含有蓖麻油的新型生物相容性微乳液,以增加塞来昔布(一种著名的消炎药)的溶解度。在这种配方中,蓖麻油还具有抗炎特性。拟议的水包油微乳剂由作为表面活性剂的吐温 80、作为辅助表面活性剂的异丁醇和作为油相的蓖麻油组成。首先,在常温下制备了表面活性剂与助表面活性剂质量比为 4 : 1 和 2 : 1 的拟议胶体系统的相图。然后,利用获得的相图,通过在微乳液区域组合不同比例的水、油、表面活性剂和助表面活性剂,选择合适的配方。然后,测定了塞来昔布在所选配方中的溶解度,并与其他已报道的微乳配方进行了比较。本部分得出的有趣结果表明,与纯水和之前提出的配方相比,塞来昔布的溶解度明显增加。这项研究的结果可用于为制药业提供基于塞来昔布生物相容性微乳剂的合适配方。
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引用次数: 0
Symmetric and Asymmetric Supercapacitor Fabrication Based on Green Synthesized NiO Nanoparticles and Graphene 基于绿色合成氧化镍纳米粒子和石墨烯的对称和不对称超级电容器制造
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-04-10 DOI: 10.1134/s1061933x23600914
A. Zemieche, L. Chetibi, D. Hamana, S. Achour, V. D. Noto

Abstract

Nickel oxide nanoparticles (NiO NPs) are synthesized using olive leaf extract (OLE), which contains a range of polyphenols. These polyphenols serve as both reducing and capping agents, stabilizing the nanoparticles. Aqueous nickel acetate is employed as a precursor. Simultaneously, exfoliated graphene (EG) is obtained via electrochemical exfoliation of graphite in aqueous solutions. These materials were employed as electroactive components in supercapacitor applications. Characterization of NiO and EG involved thermogravimetric analysis (TGA), X-ray diffraction (XRD), Raman spectroscopy (RS), X-ray photoelectron spectroscopy (XPS), and scanning/transmission electron microscopy (SEM/TEM), alongside Brunauer−Emmett−Teller (BET) analysis, confirming the formation of crystalline NiO NPs with a cubic phase and Fm-3m space group. Micrographs revealed nanoscale dimensions for both NiO and EG with a substantial surface area, as verified by BET analysis. Symmetric (NiO/NiO, EG/EG) and asymmetric (NiO/EG) supercapacitors were fabricated using the doctor blade method. Electrode evaluation, employing field-emission scanning electron microscopy FESEM, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS), demonstrated promising morphological and electrochemical characteristics. At low scan rates, both symmetric and asymmetric supercapacitors exhibited a notable gravimetric capacitance (221, 111, and 162 F g–1 at 1 mV s–1). Additionally, they revealed higher power density (173, 137, and 161 W kg–1 at 10 mV s–1), showcasing pseudocapacitive and electric double-layer capacitor (EDLC) behavior for NiO NPs and EG, respectively. This research significantly contributes valuable insights by presenting a sustainable synthesis route for NiO NPs, developing high-performance supercapacitor electrodes, and achieving a comprehensive understanding of the electrochemical behavior of NiO NPs and EG.

摘要 利用含有一系列多酚的橄榄叶提取物(OLE)合成了氧化镍纳米粒子(NiO NPs)。这些多酚既是还原剂,又是封盖剂,可稳定纳米粒子。醋酸镍水溶液被用作前体。同时,在水溶液中通过电化学剥离石墨获得剥离石墨烯(EG)。这些材料被用作超级电容器应用中的电活性成分。对氧化镍和石墨烯的表征包括热重分析 (TGA)、X 射线衍射 (XRD)、拉曼光谱 (RS)、X 射线光电子能谱 (XPS)、扫描/透射电子显微镜 (SEM/TEM),以及布鲁瑙尔-艾美特-泰勒 (BET) 分析。显微照片显示,NiO 和 EG 都具有纳米级的尺寸和相当大的表面积,BET 分析也证实了这一点。采用刮刀法制造了对称(NiO/NiO、EG/EG)和不对称(NiO/EG)超级电容器。利用场发射扫描电子显微镜(FESEM)、循环伏安法(CV)和电化学阻抗谱(EIS)对电极进行了评估,结果表明电极具有良好的形态和电化学特性。在低扫描速率下,对称和非对称超级电容器都表现出显著的重力电容(1 mV s-1 时分别为 221、111 和 162 F g-1)。此外,它们还显示出更高的功率密度(10 mV s-1 时分别为 173、137 和 161 W kg-1),分别展示了 NiO NPs 和 EG 的伪电容和双电层电容器 (EDLC) 行为。这项研究提出了一种可持续的氧化镍氮氧化物合成路线,开发了高性能超级电容器电极,并实现了对氧化镍氮氧化物和 EG 电化学行为的全面了解,因而具有重要价值。
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引用次数: 0
Kinetic Regularities of the Synthesis of Silica Nanoparticles by Heterogeneous Hydrolysis of Tetraethoxysilane Using L-Arginine as a Catalyst 以 L-精氨酸为催化剂异构水解四乙氧基硅烷合成二氧化硅纳米粒子的动力学规律性
IF 1.1 4区 化学 Q3 Chemistry Pub Date : 2024-04-10 DOI: 10.1134/s1061933x23601257
V. M. Masalov, N. S. Sukhinina, D. N. Sovyk, V. G. Ralchenko, G. A. Emel’chenko

Abstract

The kinetics of the synthesis of silica nanoparticles (<50 nm) has been studied under the conditions of heterogeneous hydrolysis of tetraethoxysilane (TEOS) using L-arginine as an alkaline catalyst. The rates of silica formation have been determined in a temperature range of 10–95°C at catalyst concentrations of 6–150 mM. It has been shown that the activation energy of the process depends on catalyst concentration and varies in a range of 21.5–13.9 kJ/mol, while decreasing linearly with increasing concentration of L-arginine in the system. The criterion of maintaining the monodispersity has been estimated for SiO2 particles being grown “onto seeds.” The density of submicron-sized silica particles has been experimentally determined as depending on the annealing temperature. Within a temperature range of 200–1000°C, the particle density varies from 2.04 to 2.20 g/cm3.

摘要 在以 L-精氨酸为碱性催化剂的四乙氧基硅烷(TEOS)异相水解条件下,研究了二氧化硅纳米粒子(50 nm)的合成动力学。在催化剂浓度为 6-150 mM、温度范围为 10-95°C 的条件下,测定了二氧化硅的形成速率。研究表明,该过程的活化能取决于催化剂浓度,变化范围为 21.5-13.9 kJ/mol,同时随着体系中 L-精氨酸浓度的增加而线性降低。对 "种子 "上生长的二氧化硅颗粒保持单分散性的标准进行了估算。亚微米级二氧化硅颗粒的密度经实验确定取决于退火温度。在 200-1000°C 的温度范围内,颗粒密度从 2.04 克/立方厘米到 2.20 克/立方厘米不等。
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引用次数: 0
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Colloid Journal
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