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This study aims to investigate the effect of hot deformation on commercially available Ti-6246 alloy below its β-transus transition temperature at 900 °C, knowing that the α → β transition temperature of Ti-6246 alloy is about 935 °C. The study systematically applies a thermomechanical processing cycle, including hot rolling at 900 °C and solution and ageing treatments at various temperatures, to investigate microstructural and mechanical alterations. The solution treatments are performed at temperatures of 800 °C, 900 °C and 1000 °C, i.e., below and above the β-transus transition temperature, for 9 min, followed by oil quenching. The ageing treatment is performed at 600 °C for 6 h, followed by air quenching. Employing various techniques, such as X-ray diffraction, scanning electron microscopy, optical microscopy, tensile strength and microhardness testing, the research identifies crucial changes in the alloy's constituent phases and morphology during thermomechanical processing. In solution treatment conditions, it was found that at temperatures of 800 °C and 900 °C, the α′-Ti martensite phase was generated in the primary α-Ti phase according to Burger's relation, but the recrystallization process was preferred at a temperature of 900 °C, while at a temperature of 1000 °C, the α″-Ti martensite phase was generated in the primary β-Ti phase according to Burger's relation. The ageing treatment conditions cause the α′-Ti/α″-Ti martensite phases to revert to their α-Ti/β-Ti primary phases. The mechanical properties, in terms of strength and ductility, underwent an important beneficial evolution when applying solution treatment, followed by ageing treatment, which provided an optimal mixture of strength and ductility. This paper provides engineers with the opportunity to understand the mechanical performance of Ti-6246 alloy under applied stresses and to improve its applications by designing highly efficient components, particularly military engine components, ultimately contributing to advances in technology and materials science. [ABSTRACT FROM AUTHOR]

C-A-S-H (CaO-Al2O3-SiO2-H2O) and N-A-S-H (Na2O-Al2O3-SiO2-H2O) have a wide range of chemical compositions and structures and are difficult to separate from alkali-activated materials. Therefore, it is difficult to analyze their microscopic properties directly. This paper reports research on the synthesis of C-A-S-H and N-A-S-H particles with an average particle size smaller than 300 nm by applying the hydrothermal method. The composition and microstructure of the products with different CaO(Na2O)/SiO2 ratios and curing conditions were characterized using XRD, the RIR method, FTIR, SEM, TEM, and laser particle size analysis. The results showed that the C-A-S-H system products with a low CaO/SiO2 ratio were mainly amorphous C-A-S-H gels. With an increase in the CaO/SiO2 ratio, an excess of Ca(OH)2 was observed at room temperature, while in a high-temperature reaction system, katoite, C4AcH11, and other crystallized products were observed. The katoite content was related to the curing temperature and the content of Ca(OH)2 and it tended to form at a high-temperature and high-calcium environment, and an increase in the temperature renders the C-A-S-H gels more compact. The main products of the N-A-S-H system at room temperature were amorphous N-A-S-H gels and a small amount of sodalite. An increase in the curing temperature promoted the formation of the crystalline products faujasite and zeolite-P. The crystallization products consisted of only zeolite-P in the high-temperature N-A-S-H system and its content were stable above 70%. An increase in the Na2O/SiO2 ratio resulted in more non-bridging oxygen and the TO4 was more isolated in the N-A-S-H structure. The composition and microstructure of the C-A-S-H and N-A-S-H system products synthesized by the hydrothermal method were closely related to the ratio of the raw materials and the curing conditions. The results of this study increase our understanding of the hydration products of alkali-activated materials. [ABSTRACT FROM AUTHOR]

Energy storage ceramics is among the most discussed topics in the field of energy research. A bibliometric analysis was carried out to evaluate energy storage ceramic publications between 2000 and 2020, based on the Web of Science (WOS) databases. This paper presents a detailed overview of energy storage ceramics research from aspects of document types, paper citations, h-indices, publish time, publications, institutions, countries/regions, research areas, highly cited papers, and keywords. A total of 3177 publications were identified after retrieval in WOS. The results show that China takes the leading position in this research field, followed by the USA and India. Xi An Jiao Tong Univ has the most publications, with the highest h-index. J.W. Zhai is the most productive author in energy storage ceramics research. Ceramics International, Journal of Materials Science-Materials in Electronics, and the Journal of Alloys and Compounds are the most productive journals in this field, and materials science—multidisciplinary is the most frequently used subject category. Keywords, highly cited papers, and the analysis of popular papers indicate that, in recent years, lead-free ceramics are prevalent, and researchers focus on fields such as the microstructure, thin films, and phase transition of ceramics. [ABSTRACT FROM AUTHOR]

Cellular automata (CA) are efficient and effective numerical tools for modeling various phenomena and processes, e.g., microstructure evolution in plastic working processes. In many cases, the analysis of phenomena can be carried out only in a limited space and on representative volume. This limitation determines the geometry of CA space hence boundary conditions are very important issues in modeling. The paper discusses different boundary conditions that can be applied to modeling. Taking into account the transformation of the modeling space, the model should allow the selection of boundary conditions. The modeling of certain phenomena and processes is directly related to changes in the geometry of a representative volume and therefore may require changes or reorganization of the modeled CA space. Four reorganization options are presented: halving, cutting and bonding, doubling, and straightening. A choice of boundary conditions may depend on particular space reorganization as used for the modeling of microstructure evolution. A set of decision rules for selecting space reorganization options taking into account the changes of CA shape and sizes is also presented. The modeling of flat and shape rolling processes utilizing some of the described techniques is shown. [ABSTRACT FROM AUTHOR]

C110 oil well casing tubes should have high strength and corrosion resistance which is commonly used for deep wells operation containing corrosive media. In this paper, the microstructure evolution of a kind of semi-macro segregation originated banded structure in casing tubes is studied under different heat treatments. It is shown that the characteristics of the banded structure will change significantly in subsequent hot working and heat treatment processes. For the hot-rolled ones, the banded structure is composed of pearlite plus bainite. After quenching, it evolves into martensite band with high concentration solute elements. Finally, the banded structure will change into a carbide banding under the following tempering process. The temperature and cooling rate of the tempering practice show an obvious effect on the final band structure. To improve anti-SSC (sulfide stress corrosion cracking) performance, the favorable QT (quenching and tempering) practice for C110 steel should be a higher tempering temperature and a quicker cooling rate, from which the banded structure defects can be decreased together with an obvious improvement of the tube wall hardness uniformity. [ABSTRACT FROM AUTHOR]

The copper current collector is an important component for lithium-ion batteries and its stability in electrolyte impacts their performance. The decomposition of LiPF6 in the electrolyte of lithium-ion batteries produces the reactive PF6, which reacts with the residual water and generates HF. In this paper, the adsorption and dissociation of H2O, HF, and PF5 on the Cu(111) surface were studied using a first-principles method based on the density functional theory. The stable configurations of HF, H2O, and PF5 adsorbed on Cu(111) and the geometric parameters of the admolecules were confirmed after structure optimization. The results showed that PF5 can promote the dissociation reaction of HF. Meanwhile, PF5 also promoted the physical adsorption of H2O on the Cu(111) surface. The CuF2 molecule was identified by determining the bond length and the bond angle of the reaction product. The energy barriers of HF dissociation on clean and O-atom-preadsorbed Cu(111) surfaces revealed that the preadsorbed O atom can promote the dissociation of HF significantly. [ABSTRACT FROM AUTHOR]

This paper is a Part I of a literature review documentation describing the currently available and used techniques that are being explored by material scientists and researchers in the field of materials characterizations and testing for both thermal and environmental barrier coatings (TBCs and EBCs, respectively). This review contains relevant information regarding the most common coating applications and their impact on the durability and life of both the coatings and the substrate materials. It also includes a description of the methodologies of coating applications and their pros and cons. A discussion of the applicability, failure modes and modeling approaches that are presently available and utilized by active researchers in the field is also included. Part II will illustrate an in-depth assessment of various aspects of the available and developing life prediction models for both TBC and EBC and the influence of intrinsic and extrinsic factors on their thermal and mechanical stability. [ABSTRACT FROM AUTHOR]