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Effect of the Temperature-Rate Regimes in Electric Pulse Plasma Sintering on Microstructure and Mechanical Properties of Aluminum Oxide: The Role of Sintering Mechanisms 电脉冲等离子体烧结中的温度-速率制度对氧化铝微观结构和机械性能的影响:烧结机制的作用
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700084
M. S. Boldin, A. A. Popov, A. V. Nokhrin, V. N. Chuvil’deev, A. A. Murashov, G. V. Shcherbak, N. Yu. Tabachkova

The temperature and heating rate affecting the shrinkage kinetics are studied for cylindrical workpieces obtained from submicron and fine aluminum oxide powder. The studies involve the powder from three batches: (1) submicron (~0.15 µm) α-Al2O3 powder, (2) submicron (~0.2 µm) α-Al2O3 powder having an amorphous layer deposited on the particle surface, and (3) fine (~1 µm) α-Al2O3 powder. It is established that the powder particles in all batches has a monocrystalline structure. The powder workpieces are sintered using the electric pulse (spark) plasma sintering (SPS) technique. The shrinkage curves are analyzed using the Young–Cutler and the Coble models. The kinetics of sintering workpieces is shown to depend on diffusion developing between the powder particles. The sintering kinetics of workpieces made from submicron powder depends on intensity of the grain-boundary diffusion. In the sintering workpieces made of finely dispersed powder, the kinetics is additionally dependent on simultaneously developing volumetric and grain-boundary diffusion. It is established that the presence of an amorphous layer on the surface of particulate α-Al2O3 having submicron size affects the rate of migration of grain interfaces and the parameters of the Coble equation at the final SPS stage. It is assumed that the accelerated growth of grains and an increase in the microhardness of samples obtained through sintering workpieces made from submicron powder with an amorphous layer on the particle surface is caused by a higher density of defects at the grain interfaces. The elevated density of defects at grain interfaces can result from crystallization of the amorphous layer.

摘要 研究了亚微米和微细氧化铝粉末制成的圆柱形工件的温度和加热速率对收缩动力学的影响。研究涉及三个批次的粉末:(1) 亚微米(约 0.15 µm)α-Al2O3 粉末;(2) 亚微米(约 0.2 µm)α-Al2O3 粉末,其颗粒表面沉积有无定形层;(3) 细(约 1 µm)α-Al2O3 粉末。所有批次的粉末颗粒都具有单晶结构。粉末工件采用电脉冲(火花)等离子烧结(SPS)技术烧结。采用 Young-Cutler 和 Coble 模型分析了收缩曲线。结果表明,工件的烧结动力学取决于粉末颗粒之间的扩散。亚微米粉末工件的烧结动力学取决于晶界扩散的强度。在由细微分散粉末制成的烧结工件中,动力学还取决于同时发展的体积扩散和晶界扩散。研究证实,亚微米级颗粒 αAl2O3 表面无定形层的存在会影响晶粒界面的迁移速度和 SPS 最后阶段的 Coble 方程参数。据推测,用亚微米粉末烧结工件获得的样品,其晶粒生长速度加快,显微硬度增加,且颗粒表面有非晶层,其原因是晶粒界面上的缺陷密度较高。晶粒界面缺陷密度升高可能是无定形层结晶的结果。
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引用次数: 0
Study of the Phase Composition and Microstructure of Complex Carbide (Ti, W)C Obtained by Spark Plasma Sintering of WC and TiC Powders 通过火花等离子烧结 WC 和 TiC 粉末获得的复合碳化物 (Ti, W)C 的相组成和显微结构研究
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700114
A. V. Terent’ev, Yu. V. Blagoveshchenskij, N. V. Isaeva, E.A. Lancev, K. E. Smetanina, A. A. Murashov, A. V. Nokhrin, M. S. Boldin, V. N. Chuvil’deev, G. V. Shcherbak

Abstract—The possibility of low-temperature in situ synthesis of (Ti, W)C using plasma-chemical WC nanopowders and industrial micron TiC powders is demonstrated. Sintering/synthesis of WC–(25, 50, and 75) wt % TiC is carried out by electric pulsed (“spark”) plasma sintering (SPS) by heating powders in a vacuum at a rate of 50°C/min to a temperature of more than 1200°C under conditions of applying a stress of 70 MPa. It is established that the synthesis proceeds most efficiently in nanopowders with an addition of 50 and 75 wt % TiC. It is shown that the joint use of plasma-chemical synthesis of nanopowders and SPS makes it possible to obtain fine-grained (with a grain size of less than 1 μm) samples with increased density and satisfactory mechanical properties (Vickers hardness is 17–18 GPa, and minimum Palmquist crack resistance coefficient is ~3 MPa m1/2).

摘要--利用等离子化学 WC 纳米粉体和工业微米 TiC 粉体低温原位合成 (Ti, W)C 的可能性得到了证实。在施加 70 兆帕应力的条件下,通过电脉冲("火花")等离子烧结(SPS),在真空中以 50°C/min 的速度将粉末加热到 1200°C 以上的温度,从而烧结/合成重量百分比为 WC-(25、50 和 75)的 TiC。结果表明,添加 50 和 75 wt % TiC 的纳米粉末的合成效率最高。结果表明,联合使用等离子体化学合成纳米粉体和 SPS 可以获得细粒样品(晶粒尺寸小于 1 μm),其密度增加,机械性能令人满意(维氏硬度为 17-18 GPa,最小帕姆奎斯特抗裂系数为 ~3 MPa m1/2)。
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引用次数: 0
Changes in the Composition and Corrosion-Electrochemical Properties of the Chromium-Nickel Steel 03Cr18Ni11 During Implantation of Argon, Oxygen, and Nitrogen Ions 铬镍钢 03Cr18Ni11 在氩、氧和氮离子注入过程中的成分和腐蚀电化学特性变化
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700047
S. G. Bystrov, S. M. Reshetnikov, A. A. Kolotov, V. Ya. Bayankin
<p>The effect of implantation of argon, oxygen, and nitrogen ions on the physicochemical structure of the surface and the corrosion and electrochemical behavior of chromium-nickel steel 03Cr18Ni11 has been studied. Methods of electrochemical polarization (EP), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS) were used. Ion implantation of argon, oxygen, and nitrogen leads to an increase in the corrosion resistance of steel 03Cr18Ni11 both in a neutral environment and in the presence of a corrosion activator (chloride anions), while irradiation with argon ions is most effective. It is found that, after implantation of argon ions, a partial etching of the steel surface occurs, i.e., an increase in the true surface. This, in turn, facilitates the onset of the passive state. At the same time, the use of oxygen and nitrogen ions leads to smoothing of the surface. AFM data indicate that the studied steel treated with argon ions exhibits the greatest resistance to local corrosion. The implantation of oxygen and argon ions reduces the overall corrosion to the greatest extent. It is important to note that deep craters and traces of pitting corrosion do not form on the surface of the steel. The XPS data show that after ion implantation, there is a change in the concentration of the elements that make up the steel in the near-surface layers of the material in the depth of the implanted layer compared with the unirradiated sample. It is established that the surface layers of steel are enriched in chromium atoms during ion implantation. This process occurs most intensively when samples are treated with argon ions. In this case, mixed chromium and iron oxides are formed, contributing to the passivation of the steel surface. Also, the process of ion implantation is accompanied by oxidation of the surface of the steel under study. This is confirmed by an increase in the oxygen content in the surface layers. To the greatest extent, this process occurs during the implantation of oxygen ions. After corrosion tests, an increased chromium content is also observed on the surface of steel treated with Ar<sup>+</sup> ions, which confirms the formation in this case of stable chromium oxides that remain on the surface during the corrosion of steel. The analysis of the fine structure of the XPS spectra showed that, under the action of argon ions, the oxygen of surface oxides is redistributed in favor of chromium atoms and the formation of stable mixed iron and chromium oxides of the spinel type, including Fe<sup>2+</sup>, Fe<sup>3+</sup>, Cr<sup>3+</sup>, and Cr<sup>6+</sup> compounds. It is important to note that, although chromium oxides are also formed during oxygen implantation and in the same quantities as during argon implantation, the protective properties of the resulting compounds are noticeably lower. Therefore, not only the chemical composition but also the structure of the resulting layers are important. It can be assumed that the high
摘要 研究了氩离子、氧离子和氮离子植入对铬镍钢 03Cr18Ni11 表面物理化学结构以及腐蚀和电化学行为的影响。研究采用了电化学极化(EP)、原子力显微镜(AFM)和 X 射线光电子能谱(XPS)等方法。氩、氧和氮的离子注入可提高 03Cr18Ni11 钢在中性环境和存在腐蚀活化剂(氯阴离子)时的耐腐蚀性,而氩离子的辐照最为有效。研究发现,植入氩离子后,钢表面会发生部分蚀刻,即真实表面增加。这反过来又促进了被动状态的出现。同时,氧离子和氮离子的使用会使表面变得平滑。原子力显微镜数据表明,用氩离子处理过的钢材具有最强的抗局部腐蚀能力。氧离子和氩离子的植入能最大程度地减少整体腐蚀。值得注意的是,钢表面没有形成深坑和点蚀痕迹。XPS 数据显示,离子注入后,与未经辐照的样品相比,构成钢的元素在材料近表层的浓度在植入层深度发生了变化。已经证实,在离子注入过程中,钢的表层富含铬原子。在用氩离子处理样品时,这一过程最为剧烈。在这种情况下,会形成铬和铁的混合氧化物,有助于钢表面的钝化。此外,在离子注入过程中,所研究钢材的表面也会发生氧化。表层氧含量的增加证实了这一点。在最大程度上,这一过程发生在氧离子植入过程中。腐蚀试验后,在用 Ar+ 离子处理过的钢材表面还观察到铬含量增加,这证实了在这种情况下形成了稳定的铬氧化物,在钢材腐蚀过程中留在表面。对 XPS 光谱精细结构的分析表明,在氩离子的作用下,表面氧化物中的氧重新分布,有利于铬原子,并形成稳定的尖晶石型铁铬混合氧化物,包括 Fe2+、Fe3+、Cr3+ 和 Cr6+ 化合物。值得注意的是,虽然在氧气植入过程中也会形成铬氧化物,且数量与氩气植入过程相同,但所形成的化合物的保护性能明显较低。因此,不仅化学成分很重要,所得层的结构也很重要。可以认为,重氩离子的高动能既影响了表面浮雕的形成,也影响了稳定的尖晶石型铁铬混合氧化物的形成。
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引用次数: 0
Surface Functionalization of Quasi-Two-Dimensional MoS2 in Nitrogen and Oxygen Plasma 氮氧等离子体中准二维 MoS2 的表面功能化
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700126
D. E. Melezhenko, D. V. Lopaev, Yu. A. Mankelevich, S. A. Khlebnikov, A. A. Solovykh, L. S. Novikov, E. N. Voronina

The effect of nitrogen and oxygen plasma on quasi-two-dimensional MoS2 films is studied experimentally and theoretically in order to identify the main mechanisms of surface functionalization and the influence on the structure and on the properties of the films. Diagnostics of samples before and after treatment using radicals and ions is carried out ex situ using Raman spectroscopy, spectroscopic ellipsometry, X‑ray photoelectron spectroscopy, etc. It is shown that the effect of the nitrogen and oxygen plasma on ultrathin MoS2 films results in modifying the near-surface layers of the samples due to removal of sulfur and incorporation of incident atoms into the resulting vacancies. The simulation of density functional theory is applied to reveal the main mechanisms of surface functionalization in MoS2 monolayers and to explain the experimental results.

摘要 通过实验和理论研究氮和氧等离子体对准二维 MoS2 薄膜的影响,以确定表面功能化的主要机制及其对薄膜结构和性能的影响。使用拉曼光谱、光谱椭偏仪、X 射线光电子能谱等对使用自由基和离子处理前后的样品进行了原位诊断。结果表明,氮和氧等离子体对超薄 MoS2 薄膜的影响导致样品的近表面层发生变化,原因是硫被去除,入射原子被纳入所产生的空位中。应用密度泛函理论模拟揭示了 MoS2 单层表面功能化的主要机制,并解释了实验结果。
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引用次数: 0
FeZrN Films: Static and Microwave Magnetic Properties FeZrN 薄膜:静态和微波磁性能
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700187
E. N. Sheftel, E. V. Harin, V. A. Tedzhetov, K. N. Rozanov, S. Yu. Bobrovskii, G. Sh. Usmanova

Abstract—The phase and structural state, parameters of the magnetic microstructure, and static and microwave magnetic properties of the Fe81–74Zr2–5N17–21 films synthesized by reactive magnetron deposition have been studied. It has been established that, as the Zr and N contents increase, the film structure changes from the so-called mixed structure (amorphous and nanocrystalline represented by the Fe-based solid solution supersaturated with zirconium and nitrogen in the bcc modification and the fcc nitride phase) to the X-ray amorphous one. The interplay of the static magnetic properties and the parameters of the stochastic magnetic structure with the effective real permeability μ' at frequencies of up to 3 GHz has been examined. It is shown that the stochastic magnetic structure determines the dynamic magnetic properties.

摘要 研究了反应磁控沉积法合成的 Fe81-74Zr2-5N17-21 薄膜的相态和结构状态、磁性微结构参数以及静态和微波磁性能。研究发现,随着锆和氮含量的增加,薄膜结构从所谓的混合结构(非晶和纳米晶,由锆和氮过饱和的 bcc 改性和 fcc 氮化物相的铁基固溶体代表)转变为 X 射线非晶结构。我们研究了静态磁性能和随机磁性结构参数与频率高达 3 GHz 的有效实际磁导率 μ' 之间的相互作用。结果表明,随机磁结构决定了动态磁特性。
{"title":"FeZrN Films: Static and Microwave Magnetic Properties","authors":"E. N. Sheftel,&nbsp;E. V. Harin,&nbsp;V. A. Tedzhetov,&nbsp;K. N. Rozanov,&nbsp;S. Yu. Bobrovskii,&nbsp;G. Sh. Usmanova","doi":"10.1134/S2075113324700187","DOIUrl":"10.1134/S2075113324700187","url":null,"abstract":"<p><b>Abstract</b>—The phase and structural state, parameters of the magnetic microstructure, and static and microwave magnetic properties of the Fe<sub>81–74</sub>Zr<sub>2–5</sub>N<sub>17–21</sub> films synthesized by reactive magnetron deposition have been studied. It has been established that, as the Zr and N contents increase, the film structure changes from the so-called mixed structure (amorphous and nanocrystalline represented by the Fe-based solid solution supersaturated with zirconium and nitrogen in the bcc modification and the fcc nitride phase) to the X-ray amorphous one. The interplay of the static magnetic properties and the parameters of the stochastic magnetic structure with the effective real permeability μ' at frequencies of up to 3 GHz has been examined. It is shown that the stochastic magnetic structure determines the dynamic magnetic properties.</p>","PeriodicalId":586,"journal":{"name":"Inorganic Materials: Applied Research","volume":"15 3","pages":"760 - 765"},"PeriodicalIF":0.5,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141252130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Properties of Coatings Based on Cerium Dioxide Obtained by Magnetron Sputtering 通过磁控溅射获得的基于二氧化铈的涂层性能
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700230
A. S. Baikin, E. O. Nasakina, A. G. Kolmakov, K. V. Sergienko, M. A. Sudarchikova, M. A. Sevostyanov

Abstract—The review presents the parameters of magnetron sputtering of coatings based on cerium dioxide and their relationship to the structure and key properties of coatings. The influence of the type of target, the introduction of oxygen into the sputtering medium, changes in sputtering power, bias voltage, type of substrate, and its temperature on the structure, mechanical properties, and hydrophobicity of CeO2-based coatings are considered.

摘要--综述介绍了基于二氧化铈的磁控溅射涂层的参数及其与涂层结构和主要性能的关系。研究了靶材类型、溅射介质中氧气的引入、溅射功率、偏置电压、基底类型及其温度的变化对二氧化铈涂层的结构、机械性能和疏水性的影响。
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引用次数: 0
Interaction of Praseodymium and Dysprosium with Oxygen in Nickel Melts at PAr = 0.1 MPa and Analysis of Nonmetallic Inclusions PAr = 0.1 兆帕时镍熔体中镨和镝与氧的相互作用及非金属夹杂物分析
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700278
V. T. Burtsev, E. B. Chabina, S. N. Anuchkin

Interaction of Pr/Dy with oxygen in nickel melts at PAr = 0.1 MPa and constant temperature was studied using the EMF instantaneous fixing method using a Mo[Cr/Cr2O3//ZrO2(MgO)//O(Nil)]Mo cell and certified sensors. Dependences a[O] = f[Pr/Dy, %] expressed in the form of logarithmic equations made it possible to compare them with each other in the concentration range of 0.001–0.2 wt % of each deoxidizer and determine that the deoxidizing ability of Pr is 1.7 times higher compared to Dy. The activity of oxygen a[O] in Ni–O–Al–(Pr/Dy) melts was calculated in comparison with Al at a concentration of 0.05 wt % of elements and its sevenfold decrease was shown for the first deoxidizer and elevenfold for the second. The morphology of nonmetallic inclusions in metallographic sections of Ni–O–Pr/Dy alloys has been studied, indicating that the inclusions are located along grain boundaries and have different configurations and a complex heterophase composition. Analysis of nonmetallic inclusions with the maximum content of deoxidizing element proved the existence of Pr/Dy oxygen compounds, which confirmed the data of thermodynamic and mass spectrometric studies. The average content of Zr in nonmetallic inclusions during the deoxidation of Pr is two times higher than in experiments during the deoxidation of Dy, which indicates the interaction of Pr/Dy with the EMF ZrO2 sensor and the preferential interaction of Pr compared to Dy and correlates with the data on the determination of a[O].

摘要在 PAr = 0.1 MPa 和恒温条件下,利用电磁场瞬时固定法,使用 Mo[Cr/Cr2O3//ZrO2(MgO)//O(Nil)]Mo 电池和经认证的传感器研究了镍熔体中 Pr/Dy 与氧气的相互作用。a[O] = f [Pr/Dy,%]以对数方程的形式表示,因此可以在每种脱氧剂的浓度为 0.001-0.2 wt % 的范围内对它们进行比较,并确定 Pr 的脱氧能力是 Dy 的 1.7 倍。在元素浓度为 0.05 wt % 时,与 Al 相比,计算了 Ni-O-Al-(Pr/Dy) 熔体中氧 a[O] 的活性,结果显示第一种脱氧剂的活性降低了 7 倍,第二种脱氧剂降低了 11 倍。对 Ni-O-Pr/Dy 合金金相切片中非金属夹杂物的形态进行了研究,结果表明夹杂物位于晶界沿线,具有不同的构型和复杂的异相成分。对脱氧元素含量最高的非金属夹杂物的分析证明了 Pr/Dy 氧化合物的存在,这也证实了热力学和质谱研究的数据。在 Pr 的脱氧过程中,非金属夹杂物中 Zr 的平均含量比在 Dy 的脱氧实验中高两倍,这表明 Pr/Dy 与 EMF ZrO2 传感器的相互作用,以及与 Dy 相比,Pr 的优先相互作用,并与测定 a[O] 的数据相关。
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引用次数: 0
Vapor Composition and Thermodynamic Characteristics of Gaseous Molecules of Alkaline Earth Metal Tungstates 碱土金属钨酸盐气态分子的蒸汽成分和热力学特性
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700357
E. K. Kazenas, N. A. Andreeva, G. K. Astakhova, V. A. Volchenkova, O. A. Ovchinnikova, T. N. Penkina, O. N. Fomina

Calculated and experimental mass spectra of gaseous tungstates of alkaline earth metals MgWO4(g), CaWO4(g), SrWO4(g), and BaWO4(g) in the temperature range from 1600 to 2000 K are presented. The partial vapor pressures are determined and equations are derived for the temperature dependences of the partial pressures of gaseous molecules of alkaline earth metal tungstates for liquids in the following form (P, atm):(log Pleft( {{text{MgW}}{{{text{O}}}_{4}}_{{left( {text{L}} right)}}} right) = - 28,737{text{/}}T + 7.95{text{ for the range from }}1600{text{ to }}1900{text{ K}};) (log Pleft( {{text{CaW}}{{{text{O}}}_{4}}_{{left( {text{L}} right)}}} right) = - 25,265{text{/}}T + 6.913{text{ for the range from }}1850{text{ to 20}}00{text{ K}};) (log Pleft( {{text{SrW}}{{{text{O}}}_{4}}_{{left( {text{L}} right)}}} right) = - 25,052{text{/}}T + 7.13{text{ for the range from }}1800{text{ to 19}}00{text{ K}};) (log Pleft( {{text{BaW}}{{{text{O}}}_{4}}_{{left( {text{L}} right)}}} right) = - 20570{text{/}}T + 4.58{text{ for the range from }}1770{text{ to 19}}00{text{ K}}{text{.}})On the basis of experimental data on vapor pressure, the enthalpies of evaporation ((Delta H_{{s,0}}^{0})), formation (( - Delta H_{{f,0}}^{0})), and atomization ((Delta H_{{{text{at}},0}}^{0})) of gaseous tungstates of alkaline earth metals are calculated, which, respectively, amount to (ΔH0, kJ/mol) 652, 890, and 2855 for MgWO4; 644, 974, and 2968 for CaWO4; 615, 1045, and 3056 for SrWO4; and 548, 1045, and 3095 for BaWO4. It is determined that the enthalpy of sublimation of alkaline earth metal tungstates decreases from magnesium to barium.

摘要 介绍了碱土金属 MgWO4(g)、CaWO4(g)、SrWO4(g) 和 BaWO4(g) 的气态钨酸盐在 1600 至 2000 K 温度范围内的计算和实验质谱。确定了碱土金属钨酸盐液体气态分子的分蒸汽压,并推导出与温度有关的方程式,其形式如下(P,atm):(log Pleft( {{text{MgW}}{{text{O}}}_{4}}}_{{left( {text{L}} right)}}}}right) = - 28737{text{/}T + 7.95{text{ for the range from }}1600text{ to }}1900{text{ K}};)(log Pleft( {{text{CaW}}{{text{O}}}_{{4}}}_{{{left( {text{L}} right)}}}}right) = - 25,265{text{/}T + 6.913text{ for the range from }}1850{text{ to 20}}00{text{K}};)(log Pleft( {{text{SrW}}{{{text{O}}}_{{4}}}_{{{left( {text{L}} right)}}} )right) = - 25052{text{/}T + 7.13{text{ for the range from }}1800text{ to 19}}00{text{ K}};)(log Pleft( {{text{BaW}}{{{text{O}}}_{{4}}}_{{{left( {text{L}} right)}}} )right) = - 20570{text{/}}T + 4.58{text{ for the range from }}1770{text{ to 19}}00{text{ K}} {text{。根据蒸汽压的实验数据,蒸发焓 ((Delta H_{{s,0}^{0})), 形成焓 (( -Delta H_{{f,0}^{0}))、和雾化((Δ H_{{text{at}},0}}^{0}/))的计算结果,对于 MgWO4,分别为(ΔH0,kJ/mol)652、890 和 2855;CaWO4:644、974 和 2968;SrWO4:615、1045 和 3056;BaWO4:548、1045 和 3095。据测定,碱土金属钨酸盐的升华焓从镁到钡依次降低。
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引用次数: 0
Properties of a High-Power Ion Beam with Particle Energy up to 1 MeV Obtained from a Plasma Created by a High-Voltage Pulse on a Graphite Cathode 从石墨阴极上高压脉冲产生的等离子体中获得的粒子能量高达 1 MeV 的大功率离子束的特性
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700102
G. V. Potemkin, A. E. Ligachev, M. V. Zhidkov

Abstract—The features of the method for generating gas-vapor plasma and the characteristics of a high-power ion beam (HPIB) obtained in a vacuum diode with a graphite cathode using a plasma-forming high-voltage nanosecond pulse are described. The cathode material and the two-pulse mode of operation of the TEMP-4 type diode make it possible to form a multicomponent nanosecond HPIB with a maximum ion energy of up to 1 MeV, a particle flux density on the surface of ~1013 ion/cm2, and a power density on the sample surface of up to 107 W/cm2 to modify the surface properties of structural materials. Materials are published within the framework of scientific discussion. The authors invite researchers of the generation of high-power beams of non-gas ions and the processes of beam modification of solid-state materials to discuss the topics of this article.

摘要--本文介绍了在带有石墨阴极的真空二极管中利用等离子体形成纳秒高压脉冲产生气相等离子体的方法的特点和获得的高功率离子束(HPIB)的特性。阴极材料和 TEMP-4 型二极管的双脉冲工作模式使得形成多组分纳秒 HPIB 成为可能,其最大离子能量高达 1 MeV,表面粒子通量密度约为 1013 个离子/cm2,样品表面功率密度高达 107 W/cm2,从而改变了结构材料的表面特性。材料在科学讨论框架内发表。作者邀请非气体离子高功率束的产生和固态材料束改性过程的研究人员讨论本文的主题。
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引用次数: 0
Mechanical Properties of Composite Rods Produced by Hot Gas Extrusion of the Nickel and Aluminum Powder Mixtures in a Steel Shell 钢壳中镍和铝粉混合物热气挤压产生的复合棒的机械性能
IF 0.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-06-03 DOI: 10.1134/S2075113324700205
F. F. Galiev, I. V. Saikov, V. D. Berbentsev, A. E. Sytschev, G. R. Nigmatullina, M. I. Alymov

Abstract—This paper presents the effect of hot gas extrusion (HGE) parameters on the phase composition and mechanical properties of composite rods composed of a core with reaction products of a Ni–Al powder mixture and a steel shell at room temperature. Composite rods are produced in three HGE modes depending on the initial extrusion temperature and the gas pressure in the chamber with parent materials. The phase composition of the produced materials is studied. It is found that the extent of the reaction of the powder mixture increases at higher temperatures of the initial HGE and, accordingly, low gas pressures, but unreacted nickel and aluminum particles remain at the lowest temperature of the initial HGE (at a higher gas pressure). Three-point bending tests show that the yield strength of the composite rod whose core contains plastic inclusions of the parent nickel and aluminum is higher than the yield strength of the steel rod. The rods with the maximum extent of the reaction are observed to have the highest microhardness.

摘要--本文介绍了热气挤压(HGE)参数对室温下由镍铝粉末混合物反应产物的芯部和钢外壳组成的复合棒的相组成和机械性能的影响。复合材料棒在三种 HGE 模式下生产,具体取决于初始挤压温度和母体材料挤压室中的气体压力。对生产材料的相组成进行了研究。研究发现,在初始 HGE 温度较高和气体压力较低的情况下,粉末混合物的反应程度会相应增加,但在初始 HGE 温度最低(气体压力较高)的情况下,未反应的镍和铝颗粒仍然存在。三点弯曲试验表明,核心含有母体镍和铝塑性夹杂物的复合材料棒的屈服强度高于钢棒的屈服强度。据观察,反应程度最大的棒材具有最高的显微硬度。
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Inorganic Materials: Applied Research
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