两组分两相分离系统的表面和界面张力

IF 1.1 4区 材料科学 Q3 METALLURGY & METALLURGICAL ENGINEERING
E. S. Zaitseva, Yu. K. Tovbin
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引用次数: 0

摘要

对二元混合物中流体和固体之间的表面张力(ST)和两个致密相之间的界面张力(IT)作为自由能过剩值的热力学决定进行了数值分析ΔF考虑相边界存在和不考虑相边界存在的两相体系。考虑立方凝析物的分层,这是以前在热力学方法中讨论过的。在引入面、边和顶点的局部表面张力的复杂边界形状的情况下,对Gibbs热力学方法的推广进行了微观分析,在数学界面上引入了表面张力。根据局部非均匀区域的平均类型,可以构造两种形式的分层分面:具有直角和光滑角。计算是在最简单的晶格气体模型(LGM)中进行的,在刚性晶格的准化学近似中考虑了最近邻的相互作用。LGM系统中双组分混合物的每个节点都可以被混合物a + B和空位V的分量所占据。计算ST和IT的两种主要方法进行了比较,它们通过\(M_{f}^{i}\)对多余自由能的不同部分贡献来表示ΔF(这里i = a, B, V为空位,1≤f≤t,其中t为不同类型节点的数量,取决于节点在立方体角落区域内的位置)。当计算固定温度下ST和IT对域大小的依赖时,根据函数类型\(M_{f}^{i}\)获得了ST和IT值的模糊性。在严格相平衡条件下,根据力学、热学和化学三个部分平衡,讨论了空位作为双组分混合物在LGM中的主要力学特性的作用。结果表明,如果在不考虑空缺的情况下对两个致密层状相进行信息技术计算,就会扭曲信息技术的实际价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Surface and Interfacial Tension of Two-Component Two-Phase Separating Systems of Cubic Shape

Surface and Interfacial Tension of Two-Component Two-Phase Separating Systems of Cubic Shape

A numerical analysis of the thermodynamic determination of the surface tension (ST) between a fluid and a solid of a binary mixture and the interfacial tension (IT) between two dense phases as an excess value of free energy is carried out ΔF two-phase system with and without taking into account the presence of a phase boundary. Stratification is considered for cubic condensates, which were previously discussed in thermodynamic approaches. A microscopic analysis is given of the generalization of the Gibbs thermodynamic approach, introducing surface tension on the mathematical interface, to the case of a complex boundary shape with the introduction of local surface tensions for faces, edges, and vertices of faces. Depending on the type of averaging of local inhomogeneous regions, two forms of layered dividing surfaces are constructed: with straight and smoothed angles. The calculation was carried out in the simplest version of the lattice gas model (LGM) taking into account the interaction of nearest neighbors in the quasi-chemical approximation on a rigid lattice. Each node of a two-component mixture in the LGM system can be occupied by the components of the mixture A + B and vacancy V. Two main methods of calculating ST and IT, which are expressed through different partial contributions of \(M_{f}^{i}\) into excess free energy ΔF (here, i = A, B, V are vacancies and 1 ≤ ft, where t is the number of different types of nodes, depending on the position of the node inside the corner regions of the cube), are compared. An ambiguity of the values of ST and IT depending on the type of functions \(M_{f}^{i}\) is obtained when calculating the dependence of ST and IT on the domain size at a fixed temperature. The role of vacancies as the main mechanical characteristic of a two-component mixture in the LGM under the condition of strict phase equilibrium according to three partial equilibria (mechanical, thermal, and chemical) is discussed. It is shown that, if calculations of the IT are carried out for two dense stratified phases without taking into account vacancies, this distorts the real value of the IT.

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来源期刊
CiteScore
1.90
自引率
18.20%
发文量
90
审稿时长
4-8 weeks
期刊介绍: Protection of Metals and Physical Chemistry of Surfaces is an international peer reviewed journal that publishes articles covering all aspects of the physical chemistry of materials and interfaces in various environments. The journal covers all related problems of modern physical chemistry and materials science, including: physicochemical processes at interfaces; adsorption phenomena; complexing from molecular and supramolecular structures at the interfaces to new substances, materials and coatings; nanoscale and nanostructured materials and coatings, composed and dispersed materials; physicochemical problems of corrosion, degradation and protection; investigation methods for surface and interface systems, processes, structures, materials and coatings. No principe restrictions exist related systems, types of processes, methods of control and study. The journal welcomes conceptual, theoretical, experimental, methodological, instrumental, environmental, and all other possible studies.
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