The high-nitrogen stainless bearing steel 30Cr15Mo1VN, possessing excellent tensile strength (~ 2466 MPa) and impact toughness (~ 130.3 J), was manufactured by pressurized induction melting and pressurized electroslag remelting (PIM + PESR) duplex process. Herein, the inclusion characteristics and element segregation of as-cast ingots, as well as the precipitate characteristics, retained austenite (RA) distribution were systematically investigated to clarify the effect of PESR on tensile and impact properties. Compared with PIM ingot, the lower quantity and larger spacing of inclusions in PIM + PESR ingot were beneficial to improving toughness. Besides, the dendrite segregation originating from solidification inherited to tempered steels and changed the multiphase structure and toughening mechanism. First, the lighter segregation (C, N, Cr, etc.) was induced by the high cooling rate, directional solidification, and short-time homogenization during PESR process, obtaining the higher contents of precipitates and RA in the PIM + PESR ingot. Second, the smaller precipitates and more RA were uniformly distributed in tempered PIM + PESR steel by alleviating segregation, obtaining better interface and matrix plasticity. Third, the dislocation densities of martensite and RA were increased by the greater precipitation pinning effect after PESR, and the uniform area ratios of close-packed and Bain groups were obtained, effectively inhibiting the propagation of secondary crack. Finally, the smaller strength difference between RA and martensite owing to lighter segregation after PESR, alleviated strain localization at phase interfaces and accommodated plastic deformation of matrix, thus, significantly enhancing the strength and toughness of the PIM+PESR steel.
{"title":"Manufacturing High Strength-Toughness High-Nitrogen Stainless Bearing Steel 30Cr15Mo1VN by Pressurized Duplex Process","authors":"Ling-Feng Xia, Hao Feng, Hua-Bing Li, Shu-Cai Zhang, Hong-Chun Zhu, Zhou-Hua Jiang","doi":"10.1007/s11663-024-03276-y","DOIUrl":"https://doi.org/10.1007/s11663-024-03276-y","url":null,"abstract":"<p>The high-nitrogen stainless bearing steel 30Cr15Mo1VN, possessing excellent tensile strength (~ 2466 MPa) and impact toughness (~ 130.3 J), was manufactured by pressurized induction melting and pressurized electroslag remelting (PIM + PESR) duplex process. Herein, the inclusion characteristics and element segregation of as-cast ingots, as well as the precipitate characteristics, retained austenite (RA) distribution were systematically investigated to clarify the effect of PESR on tensile and impact properties. Compared with PIM ingot, the lower quantity and larger spacing of inclusions in PIM + PESR ingot were beneficial to improving toughness. Besides, the dendrite segregation originating from solidification inherited to tempered steels and changed the multiphase structure and toughening mechanism. First, the lighter segregation (C, N, Cr, <i>etc.</i>) was induced by the high cooling rate, directional solidification, and short-time homogenization during PESR process, obtaining the higher contents of precipitates and RA in the PIM + PESR ingot. Second, the smaller precipitates and more RA were uniformly distributed in tempered PIM + PESR steel by alleviating segregation, obtaining better interface and matrix plasticity. Third, the dislocation densities of martensite and RA were increased by the greater precipitation pinning effect after PESR, and the uniform area ratios of close-packed and Bain groups were obtained, effectively inhibiting the propagation of secondary crack. Finally, the smaller strength difference between RA and martensite owing to lighter segregation after PESR, alleviated strain localization at phase interfaces and accommodated plastic deformation of matrix, thus, significantly enhancing the strength and toughness of the PIM+PESR steel.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142247311","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}
Pub Date : 2024-09-16DOI: 10.1007/s11663-024-03270-4
Juntao Ba, Qiuyue Zhou, Ying Ren, Lifeng Zhang
In the current study, the aggregation of CaO-Al2O3 inclusions with different CaO contents at the steel/Ar interface was in situ observed using the confocal laser scanning microscope. The critical acceleration distance and attractive force during the inclusion aggregation process were measured and calculated, and effects of inclusion composition and radius on the aggregation of inclusions were analyzed. When the CaO content in CaO-Al2O3 inclusions in 16Mn steels increased from 3 to 51 pct, inclusions gradually changed from solid to liquid. Solid and partial liquid inclusions aggregated to form large clusters with a maximum diameter of 446.2 μm. When the CaO content in inclusions increased from 3 to 26 pct, the critical acceleration distance between inclusion pairs decreased from 104.9 to 62.1 μm, and the attractive force between inclusion pairs decreased from 1.0 × 10−16 N~1.0 × 10−13 N to 1.0 × 10−18 N~1.0 × 10−15 N. As the host inclusion radius increased from 5~15 to 25~35 μm, the critical acceleration distance increased from 104.9 to 166.6 μm. For liquid inclusions, when the CaO content in inclusions increased from 38 to 51 pct, the critical deceleration distance increased from 59.7 to 93.6 μm, and the repulsive force increased from 1.0 × 10−17 N~5.0 × 10−15 N to 1.0 × 10−17 N~1.0 × 10−13 N. The liquid inclusion overcame the repulsive force and aggregated, when the host inclusion radius was larger than 10 μm, and the initial velocity of the guest inclusion was faster than 150 μm/s. The calculated attractive force between inclusions was larger than the theoretical value calculated by Kralchevsky-Paunov model.
{"title":"In Situ Observation of Aggregation of Calcium Aluminate Inclusions at Steel/Ar Interface","authors":"Juntao Ba, Qiuyue Zhou, Ying Ren, Lifeng Zhang","doi":"10.1007/s11663-024-03270-4","DOIUrl":"https://doi.org/10.1007/s11663-024-03270-4","url":null,"abstract":"<p>In the current study, the aggregation of CaO-Al<sub>2</sub>O<sub>3</sub> inclusions with different CaO contents at the steel/Ar interface was <i>in situ</i> observed using the confocal laser scanning microscope. The critical acceleration distance and attractive force during the inclusion aggregation process were measured and calculated, and effects of inclusion composition and radius on the aggregation of inclusions were analyzed. When the CaO content in CaO-Al<sub>2</sub>O<sub>3</sub> inclusions in 16Mn steels increased from 3 to 51 pct, inclusions gradually changed from solid to liquid. Solid and partial liquid inclusions aggregated to form large clusters with a maximum diameter of 446.2 μm. When the CaO content in inclusions increased from 3 to 26 pct, the critical acceleration distance between inclusion pairs decreased from 104.9 to 62.1 μm, and the attractive force between inclusion pairs decreased from 1.0 × 10<sup>−16</sup> N~1.0 × 10<sup>−13</sup> N to 1.0 × 10<sup>−18</sup> N~1.0 × 10<sup>−15</sup> N. As the host inclusion radius increased from 5~15 to 25~35 μm, the critical acceleration distance increased from 104.9 to 166.6 μm. For liquid inclusions, when the CaO content in inclusions increased from 38 to 51 pct, the critical deceleration distance increased from 59.7 to 93.6 μm, and the repulsive force increased from 1.0 × 10<sup>−17</sup> N~5.0 × 10<sup>−15</sup> N to 1.0 × 10<sup>−17</sup> N~1.0 × 10<sup>−13</sup> N. The liquid inclusion overcame the repulsive force and aggregated, when the host inclusion radius was larger than 10 μm, and the initial velocity of the guest inclusion was faster than 150 μm/s. The calculated attractive force between inclusions was larger than the theoretical value calculated by Kralchevsky-Paunov model.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142247338","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}
Pub Date : 2024-09-13DOI: 10.1007/s11663-024-03248-2
Xue-Ting Wu, Cheng-Hui Xia, Shilin Xia, Zhongwen Shi, Xiao-Gang Lu
Although single-phase diffusion triples have been adopted successfully to deduce interdiffusivities in a much wider composition range than using diffusion couples, recent studies show that diffusion quadruples can further raise efficiency covering an even broader range of compositions than triples. In the present work, two diffusion quadruples of the fcc Co–Ni–Ta alloy system were assembled at 1473 K, allowing for a direct comparison with the former triple scheme. The composition-dependent interdiffusivities were then deduced, and mutually validated by comparing with the results calculated from the triple scheme and the traditional methods (i.e., the Sauer–Freise method and Whittle–Green method). To ensure the universality of the quadruple scheme, one diffusion quadruple was fabricated under universal preparation conditions without strict requirements of the original interfaces. By updating our two-dimensional (2D) numerical inverse scheme, the present quadruple scheme can well handle general cases with both ideal and universal original interfaces. However, since the absolute deviation is not significant and the results obtained by the quadruple scheme are fine-tuning of those from the triple scheme, both the triple and quadruple schemes are acceptable for engineering applications.
{"title":"Diffusion Quadruple vs Triple: Determining Interdiffusivities for fcc Co–Ni–Ta Alloys","authors":"Xue-Ting Wu, Cheng-Hui Xia, Shilin Xia, Zhongwen Shi, Xiao-Gang Lu","doi":"10.1007/s11663-024-03248-2","DOIUrl":"https://doi.org/10.1007/s11663-024-03248-2","url":null,"abstract":"<p>Although single-phase diffusion triples have been adopted successfully to deduce interdiffusivities in a much wider composition range than using diffusion couples, recent studies show that diffusion quadruples can further raise efficiency covering an even broader range of compositions than triples. In the present work, two diffusion quadruples of the fcc Co–Ni–Ta alloy system were assembled at 1473 K, allowing for a direct comparison with the former triple scheme. The composition-dependent interdiffusivities were then deduced, and mutually validated by comparing with the results calculated from the triple scheme and the traditional methods (<i>i.e</i>., the Sauer–Freise method and Whittle–Green method). To ensure the universality of the quadruple scheme, one diffusion quadruple was fabricated under universal preparation conditions without strict requirements of the original interfaces. By updating our two-dimensional (2D) numerical inverse scheme, the present quadruple scheme can well handle general cases with both ideal and universal original interfaces. However, since the absolute deviation is not significant and the results obtained by the quadruple scheme are fine-tuning of those from the triple scheme, both the triple and quadruple schemes are acceptable for engineering applications.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142247312","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}
The stable control of mold level is a key link in the production of high-quality continuous casting slabs. Periodic mold level fluctuation (PMLF) is common during the continuous casting process, and the abnormal PMLF has significant harmful effects on surface quality of slab. This article proposed an analysis and control method for abnormal PMLF. First, the finite impulse response (FIR) filter and fast Fourier transform (FFT) were used to remove noise interference in PMLF data and highlight the fluctuation characteristics of PMLM. Then, considering that uneven solidification has a significant impact on abnormal PMLF, the influence of chemical composition on the equilibrium Fe-C pseudo-binary diagram was calculated by Thermo-Calc software. Furthermore, roller diameter, roller spacing, casting speed, and chemical composition were chosen as the prediction indicator to predict the quality of PMLF. Random forest (RF) model shows good performance in predicting PMLF; the prediction accuracy of RF model is 92.76 pct, which is 21.39 pct higher than that of GA-BP model. Finally, the Feedforward fuzzy PID (F2FPID) controller designed in this article was used to eliminate abnormal PMLF. The average range of mold level fluctuation under the PID controller is ± 6.8 mm, while under the F2FPID controller, the average range of mold level fluctuation is ± 1.1 mm. And the F2FPID controller owns a lower overshoot of 0.48 pct and an adjusting time of 1.52 seconds, which are 94.8 pct and 59.5 pct, respectively, lower than those of the PID controller.
{"title":"Characterizing and Controlling Abnormal Periodic Mold Level Fluctuations in a Commercial Slab Continuous Caster Using Big Data","authors":"Xiaoliang Meng, Sen Luo, Xiaobo Xi, Yelian Zhou, Weiling Wang, Miaoyong Zhu","doi":"10.1007/s11663-024-03275-z","DOIUrl":"https://doi.org/10.1007/s11663-024-03275-z","url":null,"abstract":"<p>The stable control of mold level is a key link in the production of high-quality continuous casting slabs. Periodic mold level fluctuation (PMLF) is common during the continuous casting process, and the abnormal PMLF has significant harmful effects on surface quality of slab. This article proposed an analysis and control method for abnormal PMLF. First, the finite impulse response (FIR) filter and fast Fourier transform (FFT) were used to remove noise interference in PMLF data and highlight the fluctuation characteristics of PMLM. Then, considering that uneven solidification has a significant impact on abnormal PMLF, the influence of chemical composition on the equilibrium Fe-C pseudo-binary diagram was calculated by Thermo-Calc software. Furthermore, roller diameter, roller spacing, casting speed, and chemical composition were chosen as the prediction indicator to predict the quality of PMLF. Random forest (RF) model shows good performance in predicting PMLF; the prediction accuracy of RF model is 92.76 pct, which is 21.39 pct higher than that of GA-BP model. Finally, the Feedforward fuzzy PID (F2FPID) controller designed in this article was used to eliminate abnormal PMLF. The average range of mold level fluctuation under the PID controller is ± 6.8 mm, while under the F2FPID controller, the average range of mold level fluctuation is ± 1.1 mm. And the F2FPID controller owns a lower overshoot of 0.48 pct and an adjusting time of 1.52 seconds, which are 94.8 pct and 59.5 pct, respectively, lower than those of the PID controller.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142247337","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}
Pub Date : 2024-09-13DOI: 10.1007/s11663-024-03269-x
Renyi Yang, Wanlin Wang, Chenyang Zhu, Jie Zeng
Strip casting casts molten steel into thin strips, enabling direct hot rolling to produce products. A typical hot stamping steel thin strip was made by a strip casting simulator under tailored casting and hot rolling temperatures. The casting strip showed improved surface quality at a higher casting temperature (1597 °C) and a lower rolling temperature (900 °C), achieving 1275 MPa tensile strength with 12.3 pct elongation due to refined austenite grains transforming to martensite.
{"title":"Tailored Casting and Hot Rolling Temperatures for the Preparation of Hot Stamping Steel Thin Strip","authors":"Renyi Yang, Wanlin Wang, Chenyang Zhu, Jie Zeng","doi":"10.1007/s11663-024-03269-x","DOIUrl":"https://doi.org/10.1007/s11663-024-03269-x","url":null,"abstract":"<p>Strip casting casts molten steel into thin strips, enabling direct hot rolling to produce products. A typical hot stamping steel thin strip was made by a strip casting simulator under tailored casting and hot rolling temperatures. The casting strip showed improved surface quality at a higher casting temperature (1597 °C) and a lower rolling temperature (900 °C), achieving 1275 MPa tensile strength with 12.3 pct elongation due to refined austenite grains transforming to martensite.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"94 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142247334","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}
Pub Date : 2024-09-12DOI: 10.1007/s11663-024-03262-4
Qijia Yang, Shiliang Yang, Junyi Hu, Hua Wang
The multi-lance top-blown converting furnace is pivotal in the converting process of molten white matte (copper content nearly 75 pct) in continuous copper smelting technology. The complex multiphase hydrodynamics and phase interaction mechanisms inherent in this furnace significantly influence converting efficiency of blister copper. This study numerically explores the intricate gas–melt flow hydrodynamics and stirring dynamics in the multi-lance top-blown converting furnace based on the OpenFOAM platform. Following model validation, this study elucidates various aspects of bath dynamics in the furnace. The findings reveal that the arrangement of multiple lances along the longitudinal axis introduces an offset effect on longitudinal momentum transfer and a superposition effect on transverse momentum transfer, unlike the single-lance blowing configuration. A linear empirical relationship between jet momentum number and length group under multi-lance top blowing is established, with a determined constant value of 3.65 for turbulent gas jet. Additionally, a strong correlation between dimensionless cavity shape index and the kinetic energy of molten slag is observed, leading to the formulation of a functional relationship equation demonstrating exponential growth: Eb = exp(− 2.81011–0.79077 ({I}_{text{cm}}) + 0.13479 ({{I}_{text{cm}}}^{2})). Moreover, both the internal flow of molten bath and the shear stress on the furnace wall exhibit a step-like periodic oscillation mode. Notably, based on the similarity observed in the main frequency peaks, a robust correlation between the two phenomena is inferred. Under conditions of small lance spacing and diameter, an increase in the cavity aspect ratio enhances momentum transfer efficiency and stirring performance of bath, but it also exacerbates erosion of the lances and the furnace. This study elucidates the multiphase mixing characteristics, phase interaction mechanisms, and furnace wall erosion patterns in a multi-lance top-blown converting furnace, providing a crucial theoretical foundation for the design, operation, and optimization of such systems.
{"title":"Complex Multiphase Coupling Mechanisms in the Multi-lance Top-Blown Copper Converting Furnace","authors":"Qijia Yang, Shiliang Yang, Junyi Hu, Hua Wang","doi":"10.1007/s11663-024-03262-4","DOIUrl":"https://doi.org/10.1007/s11663-024-03262-4","url":null,"abstract":"<p>The multi-lance top-blown converting furnace is pivotal in the converting process of molten white matte (copper content nearly 75 pct) in continuous copper smelting technology. The complex multiphase hydrodynamics and phase interaction mechanisms inherent in this furnace significantly influence converting efficiency of blister copper. This study numerically explores the intricate gas–melt flow hydrodynamics and stirring dynamics in the multi-lance top-blown converting furnace based on the OpenFOAM platform. Following model validation, this study elucidates various aspects of bath dynamics in the furnace. The findings reveal that the arrangement of multiple lances along the longitudinal axis introduces an offset effect on longitudinal momentum transfer and a superposition effect on transverse momentum transfer, unlike the single-lance blowing configuration. A linear empirical relationship between jet momentum number and length group under multi-lance top blowing is established, with a determined constant value of 3.65 for turbulent gas jet. Additionally, a strong correlation between dimensionless cavity shape index and the kinetic energy of molten slag is observed, leading to the formulation of a functional relationship equation demonstrating exponential growth: <b><i>E</i></b><sub><i>b</i></sub> = exp(− 2.81011–0.79077 <span>({I}_{text{cm}})</span> + 0.13479 <span>({{I}_{text{cm}}}^{2})</span>). Moreover, both the internal flow of molten bath and the shear stress on the furnace wall exhibit a step-like periodic oscillation mode. Notably, based on the similarity observed in the main frequency peaks, a robust correlation between the two phenomena is inferred. Under conditions of small lance spacing and diameter, an increase in the cavity aspect ratio enhances momentum transfer efficiency and stirring performance of bath, but it also exacerbates erosion of the lances and the furnace. This study elucidates the multiphase mixing characteristics, phase interaction mechanisms, and furnace wall erosion patterns in a multi-lance top-blown converting furnace, providing a crucial theoretical foundation for the design, operation, and optimization of such systems.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"93 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208276","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}
The vacuum carbon deoxidation process via CO formation has the ability to achieve high cleanliness of nickel alloys in vacuum induction melting. In the present study, the effect of vacuum degree in melting chamber, melt temperature, and initial carbon content on deoxidation efficiency was studied. The reactions of vacuum carbon deoxidization and MgO decomposition were strongly affected by chamber pressure and melt temperature. Low chamber pressure and high melt temperature resulted in a severe MgO-crucible decomposition reaction and increased oxygen supply to molten nickel alloy, and hence, decreased the deoxidation efficiency. Therefore, moderate vacuum degree in the chamber and lower melt temperature would improve the vacuum carbon deoxidation efficiency. The reaction rates of vacuum carbon deoxidization and MgO decomposition were controlled by the mass transfer of oxygen in liquid boundary layers near the reaction interfaces. The nitrogen in molten nickel alloy could be well removed together with carbon deoxidation under the vacuum conditions in the present study. A prediction model of deoxidation and carbon loss in vacuum melting process was established to determine the optimum temperature and vacuum conditions in vacuum carbon deoxidation process.
通过 CO 生成的真空碳脱氧工艺能够在真空感应熔炼中实现镍合金的高清洁度。本研究探讨了熔炼室真空度、熔体温度和初始碳含量对脱氧效率的影响。真空碳脱氧和氧化镁分解反应受到腔室压力和熔体温度的强烈影响。低真空室压力和高熔体温度会导致严重的氧化镁脆性分解反应,增加熔融镍合金的供氧量,从而降低脱氧效率。因此,适度的真空室真空度和较低的熔体温度会提高真空碳脱氧效率。真空碳脱氧和氧化镁分解的反应速率受反应界面附近液体边界层中氧的传质控制。在本研究中,在真空条件下,熔融镍合金中的氮能与碳脱氧一起被很好地去除。建立了真空熔炼过程中脱氧和碳损失的预测模型,以确定真空碳脱氧过程中的最佳温度和真空条件。
{"title":"Deoxidation of Nickel-based Superalloy Using Carbon under High Vacuum Degree","authors":"Xu-Ze Li, Hao Feng, Hua-Bing Li, Shou-Xing Yang, Shu-Cai Zhang, Hong-Chun Zhu, Jong-Jin Pak, Zhou-Hua Jiang","doi":"10.1007/s11663-024-03258-0","DOIUrl":"https://doi.org/10.1007/s11663-024-03258-0","url":null,"abstract":"<p>The vacuum carbon deoxidation process <i>via</i> CO formation has the ability to achieve high cleanliness of nickel alloys in vacuum induction melting. In the present study, the effect of vacuum degree in melting chamber, melt temperature, and initial carbon content on deoxidation efficiency was studied. The reactions of vacuum carbon deoxidization and MgO decomposition were strongly affected by chamber pressure and melt temperature. Low chamber pressure and high melt temperature resulted in a severe MgO-crucible decomposition reaction and increased oxygen supply to molten nickel alloy, and hence, decreased the deoxidation efficiency. Therefore, moderate vacuum degree in the chamber and lower melt temperature would improve the vacuum carbon deoxidation efficiency. The reaction rates of vacuum carbon deoxidization and MgO decomposition were controlled by the mass transfer of oxygen in liquid boundary layers near the reaction interfaces. The nitrogen in molten nickel alloy could be well removed together with carbon deoxidation under the vacuum conditions in the present study. A prediction model of deoxidation and carbon loss in vacuum melting process was established to determine the optimum temperature and vacuum conditions in vacuum carbon deoxidation process.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"60 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208275","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}
Efficient and stable lithium-ion batteries (LIBs) have garnered considerable attention; yet, the development of anode electrode materials continues to pose substantial challenges. While CoO electrode material boasts an ideal specific theoretical capacity, it is not without drawbacks, including significant volume expansion and concerns over safety performance, which hinder its viability as an anode material. In this research, we synthesized CoO/Co3O4 through a straightforward secondary hydrothermal treatment that locally oxidizes CoO, simultaneously creating oxygen vacancies. The incorporation of oxygen vacancies enhances the material’s internal conductivity and expedites the diffusion of electrons and ions, culminating in superior rate performance. Furthermore, the heterojunction structure diminishes the diffusion barrier, significantly enhancing the electrode’s reaction kinetics and overall electrochemical performance. At a modest current density of 0.1 A g−1, the CoO/Co3O4 composite demonstrates enhanced cycling stability, delivering a capacity of 1022 mAh g−1 after 100 cycles. Remarkably, even at an elevated current density of 1 A g−1, it sustains a capacity of 768.8 mAh g−1 over 400 cycles. The method of creating oxygen vacancies via autoxidation may pave the way for the advancement of multivalent oxide anode materials.
高效、稳定的锂离子电池(LIB)备受关注,但负极电极材料的开发仍面临巨大挑战。尽管 CoO 电极材料拥有理想的比理论容量,但它也并非没有缺点,包括显著的体积膨胀和对安全性能的担忧,这些都阻碍了它作为负极材料的可行性。在这项研究中,我们通过直接的二次水热处理合成了 CoO/Co3O4,在局部氧化 CoO 的同时产生了氧空位。氧空位的加入增强了材料的内部电导率,加快了电子和离子的扩散,从而实现了卓越的速率性能。此外,异质结结构减小了扩散障碍,显著提高了电极的反应动力学和整体电化学性能。在 0.1 A g-1 的适度电流密度下,CoO/Co3O4 复合材料显示出更强的循环稳定性,100 次循环后可提供 1022 mAh g-1 的容量。值得注意的是,即使在 1 A g-1 的高电流密度下,它也能在 400 次循环后保持 768.8 mAh g-1 的容量。通过自氧化产生氧空位的方法可能会为多价氧化物阳极材料的发展铺平道路。
{"title":"Improvement of Electrochemical Performance of Lithium-Ion Anode Materials by Local Oxidation of Multivalent Metal Oxides (CoO)","authors":"Zhiqiang Liu, Hui Li, Zhiteng Wang, Xiaobing Li, Huixin Lan, Zhenhe Zhu, Yi Zhuang, Yuchen Wu, Jiajia Li, Huan Yao, Runbo Gao","doi":"10.1007/s11663-024-03271-3","DOIUrl":"https://doi.org/10.1007/s11663-024-03271-3","url":null,"abstract":"<p>Efficient and stable lithium-ion batteries (LIBs) have garnered considerable attention; yet, the development of anode electrode materials continues to pose substantial challenges. While CoO electrode material boasts an ideal specific theoretical capacity, it is not without drawbacks, including significant volume expansion and concerns over safety performance, which hinder its viability as an anode material. In this research, we synthesized CoO/Co<sub>3</sub>O<sub>4</sub> through a straightforward secondary hydrothermal treatment that locally oxidizes CoO, simultaneously creating oxygen vacancies. The incorporation of oxygen vacancies enhances the material’s internal conductivity and expedites the diffusion of electrons and ions, culminating in superior rate performance. Furthermore, the heterojunction structure diminishes the diffusion barrier, significantly enhancing the electrode’s reaction kinetics and overall electrochemical performance. At a modest current density of 0.1 A g<sup>−1</sup>, the CoO/Co<sub>3</sub>O<sub>4</sub> composite demonstrates enhanced cycling stability, delivering a capacity of 1022 mAh g<sup>−1</sup> after 100 cycles. Remarkably, even at an elevated current density of 1 A g<sup>−1</sup>, it sustains a capacity of 768.8 mAh g<sup>−1</sup> over 400 cycles. The method of creating oxygen vacancies <i>via</i> autoxidation may pave the way for the advancement of multivalent oxide anode materials.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"71 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208277","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}
Pub Date : 2024-09-10DOI: 10.1007/s11663-024-03253-5
Osamu Takeda, Xin Lu, Hongmin Zhu
As the production of high-quality titanium (Ti) metal increases significantly, the generation of low-quality Ti scraps increases and exceeds the demand for current cascade recycling in ferrous metallurgy. Therefore, the development of an upgrading recycling technology, in which scraps are refined and reutilized, is required. The magnesium (Mg) deoxidation assisted by the formation of oxychlorides of rare earth metals is currently considered a promising process for upgrading recycling technology, during which YOCl is formed as a byproduct. In this study, we investigate the synthesis and separation of YCl3 from YOCl via carbochlorination at 973 and 1073 K and confirmed that YCl3 can be regenerated from YOCl at a high conversion rate (82.7 pct at maximum). YCl3 was also formed even in the presence of MgCl2; however, MgCl2 decreased the conversion rate (49.8 pct at minimum). The conversion rate in the temperature region where YCl3 is a liquid (1073 K) was lower than that in the temperature region where YCl3 is a solid (973 K). Therefore, an operation with temperature cycling, in which YCl3 is formed at a temperature where YCl3 is a solid and then the temperature is increased to a temperature where YCl3 is a liquid to drain the molten mixed salt, is efficient.
{"title":"Carbochlorination of YOCl for Synthesis of YCl3","authors":"Osamu Takeda, Xin Lu, Hongmin Zhu","doi":"10.1007/s11663-024-03253-5","DOIUrl":"https://doi.org/10.1007/s11663-024-03253-5","url":null,"abstract":"<p>As the production of high-quality titanium (Ti) metal increases significantly, the generation of low-quality Ti scraps increases and exceeds the demand for current cascade recycling in ferrous metallurgy. Therefore, the development of an upgrading recycling technology, in which scraps are refined and reutilized, is required. The magnesium (Mg) deoxidation assisted by the formation of oxychlorides of rare earth metals is currently considered a promising process for upgrading recycling technology, during which YOCl is formed as a byproduct. In this study, we investigate the synthesis and separation of YCl<sub>3</sub> from YOCl <i>via</i> carbochlorination at 973 and 1073 K and confirmed that YCl<sub>3</sub> can be regenerated from YOCl at a high conversion rate (82.7 pct at maximum). YCl<sub>3</sub> was also formed even in the presence of MgCl<sub>2</sub>; however, MgCl<sub>2</sub> decreased the conversion rate (49.8 pct at minimum). The conversion rate in the temperature region where YCl<sub>3</sub> is a liquid (1073 K) was lower than that in the temperature region where YCl<sub>3</sub> is a solid (973 K). Therefore, an operation with temperature cycling, in which YCl<sub>3</sub> is formed at a temperature where YCl<sub>3</sub> is a solid and then the temperature is increased to a temperature where YCl<sub>3</sub> is a liquid to drain the molten mixed salt, is efficient.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"58 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208278","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}
Improving the corrosion resistance of carbon steel is of great importance to realize widely use in various industries. The anti-corrosion coating is a significant protective strategy. Therefore, uniform aluminum coatings (AlOx-CS), electrodepositing in ionic liquid electrolyte at room temperature, was developed to enhance corrosion resistance of carbon steel. The lower part of the electrode has a better distribution uniformity than the upper part of the electrode, and the distribution of a line has the lowest variance. The uniform AlOx-CS coating is the most corrosion resistant due to sealed Al2O3 layers. The corrosion rate of the AlOx-CS coating is 0.4 mm a−1. The self-corrosion current density of AlOx-CS coating is 34.4 μA cm−2, nearly 2 times compared with pristine carbon steel. The impedance value with AlOx-CS coating is increased by nearly 300 times compared with pristine carbon steel. The morphology and composition of aluminum-based reinforced coatings had no significant changes in atmospheric exposure, 3.5 pct NaCl salt spray and 3.5 pct NaCl immersion environments. The aluminum-based reinforced coatings can enhance the lifespan of carbon steel materials, while also reducing economic losses and safety hazards.
{"title":"Improving the Corrosion Resistance of Carbon Steel Via Aluminum-Based Coating from Ionic Liquid Electrolytes at Room Temperature","authors":"Wen Wang, Na Li, Zhiyuan Li, Li-li Jiang, Wei-Li Song, Mingyong Wang, Shuqiang Jiao","doi":"10.1007/s11663-024-03260-6","DOIUrl":"https://doi.org/10.1007/s11663-024-03260-6","url":null,"abstract":"<p>Improving the corrosion resistance of carbon steel is of great importance to realize widely use in various industries. The anti-corrosion coating is a significant protective strategy. Therefore, uniform aluminum coatings (AlO<sub><i>x</i></sub>-CS), electrodepositing in ionic liquid electrolyte at room temperature, was developed to enhance corrosion resistance of carbon steel. The lower part of the electrode has a better distribution uniformity than the upper part of the electrode, and the distribution of a line has the lowest variance. The uniform AlO<sub><i>x</i></sub>-CS coating is the most corrosion resistant due to sealed Al<sub>2</sub>O<sub>3</sub> layers. The corrosion rate of the AlO<sub><i>x</i></sub>-CS coating is 0.4 mm a<sup>−1</sup>. The self-corrosion current density of AlO<sub><i>x</i></sub>-CS coating is 34.4 <i>μ</i>A cm<sup>−2</sup>, nearly 2 times compared with pristine carbon steel. The impedance value with AlO<sub><i>x</i></sub>-CS coating is increased by nearly 300 times compared with pristine carbon steel. The morphology and composition of aluminum-based reinforced coatings had no significant changes in atmospheric exposure, 3.5 pct NaCl salt spray and 3.5 pct NaCl immersion environments. The aluminum-based reinforced coatings can enhance the lifespan of carbon steel materials, while also reducing economic losses and safety hazards.</p>","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"17 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208306","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}