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Unveiling the Mechanism of Aluminum Removing Vanadium from Crude Titanium Tetrachloride Via Deep Potential Molecular Dynamics Simulation 用深电位分子动力学模拟揭示铝从粗四氯化钛中除钒机理
Pub Date : 2025-05-08 DOI: 10.1007/s11663-025-03530-x
Jie Zhou, Yan Feng, Xiumin Chen, Enhao Zhang, Huapeng Wu, Yunmin Chen, Haiguang Huang, Jianjun Li, Qian Yang
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引用次数: 1
Role of Minor Elements on Phase and Composition Evolutions of Iron–Vanadium Spinels Upon Calcium Roasting 微量元素对钙焙烧铁钒尖晶石物相及组成演变的影响
Pub Date : 2025-03-14 DOI: 10.1007/s11663-025-03496-w
Jianqi Cao, Shanshan Feng, Wanlin Wang, Daoyuan Huang, Yongqi Sun
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引用次数: 3
Phase Equilibria of the Mn3O4–SiO2–CaO(–Al2O3) System in Air at 1573 K and 1673 K 1573 K和1673 K空气中Mn3O4-SiO2-CaO (-Al2O3)体系的相平衡
Pub Date : 2025-01-27 DOI: 10.1007/s11663-025-03439-5
Yuxuan Zeng, Mengjie Ran, Songwen Xiao, Zhihong Liu, Guoxing Ren
{"title":"Phase Equilibria of the Mn3O4–SiO2–CaO(–Al2O3) System in Air at 1573 K and 1673 K","authors":"Yuxuan Zeng, Mengjie Ran, Songwen Xiao, Zhihong Liu, Guoxing Ren","doi":"10.1007/s11663-025-03439-5","DOIUrl":"https://doi.org/10.1007/s11663-025-03439-5","url":null,"abstract":"","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"56 2","pages":"1617-1628"},"PeriodicalIF":0.0,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332517","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: 1
Phase and Structure Evolutions of Iron-Rich Zinc-Bearing Spinel During Calcium Sintering 富铁含锌尖晶石在钙烧结过程中的相与结构演变
Pub Date : 2025-01-07 DOI: 10.1007/s11663-024-03421-7
Shanshan Feng, Shuxuan Luo, Wanlin Wang, Daoyuan Huang, Yongqi Sun
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引用次数: 3
Phase Relations of “FeO”–SiO2–CaO–V2O3 System: Basic Research on Vanadium Slag “FeO”-SiO2-CaO-V2O3体系的相关系:钒渣的基础研究
Pub Date : 2024-11-25 DOI: 10.1007/s11663-024-03380-z
Guoliang Feng, Jintao Gao, Xi Lan, Zhancheng Guo
{"title":"Phase Relations of “FeO”–SiO2–CaO–V2O3 System: Basic Research on Vanadium Slag","authors":"Guoliang Feng, Jintao Gao, Xi Lan, Zhancheng Guo","doi":"10.1007/s11663-024-03380-z","DOIUrl":"https://doi.org/10.1007/s11663-024-03380-z","url":null,"abstract":"","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"56 1","pages":"660-673"},"PeriodicalIF":0.0,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147330418","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: 5
Reaction Mechanism and Technical Application of Recovery FeAs, Sb, and Na2CO3 from Arsenic-Alkali Residue 从砷碱渣中回收FeAs、Sb和Na2CO3的反应机理及技术应用
Pub Date : 2024-11-25 DOI: 10.1007/s11663-024-03382-x
Shi‐Yang Tang, Jianguang Yang, Tianxiang Nan, Qiang Zhu, Jiang Liu, Rongbo Zhu, An-bang Su, Xing Fan, Chaobo Tang
{"title":"Reaction Mechanism and Technical Application of Recovery FeAs, Sb, and Na2CO3 from Arsenic-Alkali Residue","authors":"Shi‐Yang Tang, Jianguang Yang, Tianxiang Nan, Qiang Zhu, Jiang Liu, Rongbo Zhu, An-bang Su, Xing Fan, Chaobo Tang","doi":"10.1007/s11663-024-03382-x","DOIUrl":"https://doi.org/10.1007/s11663-024-03382-x","url":null,"abstract":"","PeriodicalId":18613,"journal":{"name":"Metallurgical and Materials Transactions B","volume":"56 1","pages":"674-686"},"PeriodicalIF":0.0,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147330495","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
Electrochemical Reduction Behavior of Pure Metal Oxides Without Supporting Electrolytes at Ultrahigh Temperatures 无支撑电解质的纯金属氧化物在超高温下的电化学还原行为
Pub Date : 2024-11-20 DOI: 10.1007/s11663-024-03357-y
Yiming Yan, Guangshi Li, Bohao Yang, Pengfei Zhao, Peiyan Huang, Xing Yu, Zhongya Pang, Qian Xu, Xionggang Lu, Xingli Zou
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引用次数: 0
Production of Low-Oxygen Ti Powder by Magnesiothermic Reduction of TiO2 in MgCl2–KCl–CeCl3 Molten Salt 在 MgCl2-KCl-CeCl3 熔盐中通过镁热还原 TiO2 生产低氧钛粉末
Pub Date : 2024-09-17 DOI: 10.1007/s11663-024-03251-7
Liguo Zhu, Zuqing Zhang, Lingxin Kong, Chengyuan Wang, Bin Yang, Baoqiang Xu

Ti is produced by the Kroll method, mainly by carbothermic chlorination, magnesiothermic reduction, and vacuum distillation, which result in complex processes, low efficiency, and high cost. Although Ti has many excellent properties, its high production costs limit its widespread applications. There is an urgent need to develop new Ti extraction processes to reduce the cost of Ti production. In this study, we propose a new method for the direct preparation of low-oxygen Ti powder from TiO2 using Mg as a reducing agent and the formation of CeOCl (2Mg (l) + TiO2 (s) + 2CeCl3 (l) = Ti (s) + 2CeOCl (s) + 2MgCl2 (l)). First, a deoxidization experiment of Ti with Mg as a deoxidizer was conducted, and the ability of Mg to deoxidize Ti was demonstrated. At 1273 K, when the activity of CeCl3 was 1, the oxygen concentrations of Ti-A and Ti-B were 380 and 270 ppm, respectively. Subsequently, the TiO2 reduction experiment was conducted using Mg as the reducing agent. The results showed that MgO activity was effectively reduced by the formation of CeOCl (MgO(s) + CeCl3(l) = MgCl2(l) + CeOCl(s)). When the system reached the Mg/MgCl2/CeOCl/CeCl3 equilibrium, low-oxygen Ti powder below 1000 ppm was directly produced from TiO2.

钛是通过克罗尔法生产的,主要是通过碳热氯化、镁热还原和真空蒸馏,工艺复杂、效率低、成本高。虽然钛具有许多优异的性能,但其高昂的生产成本限制了它的广泛应用。因此迫切需要开发新的钛提取工艺来降低钛的生产成本。在本研究中,我们提出了一种以 Mg 为还原剂并形成 CeOCl(2Mg (l) + TiO2 (s) + 2CeCl3 (l) = Ti (s) + 2CeOCl (s) + 2MgCl2 (l)),直接从 TiO2 制备低氧 Ti 粉末的新方法。首先,以 Mg 为脱氧剂对 Ti 进行了脱氧实验,证明了 Mg 对 Ti 的脱氧能力。在 1273 K 时,当 CeCl3 的活性为 1 时,Ti-A 和 Ti-B 的氧浓度分别为 380 和 270 ppm。随后,以 Mg 为还原剂进行了 TiO2 还原实验。结果表明,CeOCl 的形成有效地降低了 MgO 的活性(MgO(s) + CeCl3(l) = MgCl2(l) + CeOCl(s))。当系统达到 Mg/MgCl2/CeOCl/CeCl3 平衡时,TiO2 可直接生成低于 1000 ppm 的低氧 Ti 粉末。
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引用次数: 0
Synergistic Effect of Graphite and Fly Ash on the Microstructural Evolution and Tribological Characteristics of Fe-Cu-Based Wind Turbine-Sintered Brake Pad Materials 石墨和粉煤灰对铁铜基风力涡轮机烧结刹车片材料微结构演变和摩擦学特性的协同效应
Pub Date : 2024-09-17 DOI: 10.1007/s11663-024-03273-1
K. Rajesh Kannan, R. Vaira Vignesh, M. Govindaraju, T. Ram Prabhu, Abd Baghad

The research focused on the effect of graphite proportion and the incorporation of fly ash in Fe-Cu-based friction materials produced via powder metallurgy technique. Microstructural investigation of the specimens demonstrated the homogenous distribution of the secondary element (Cu), lubricant (graphite), and reinforcements (fly ash) in the matrix (Fe). A maximum density of 5.7 g/cm3 was attained for the specimens, with an overall density of 70 pct of theoretical density. FM03 specimens showed a better wear resistance of 4.7 × 10−8 g/Nm with an optimum coefficient of friction of 0.4. The specific wear rate of the conventional friction material was 97.7 pct higher than the FM03 specimens.

Graphical Abstract

研究重点是通过粉末冶金技术生产的铁铜基摩擦材料中石墨比例和粉煤灰加入量的影响。试样的微观结构研究表明,次要元素(铜)、润滑剂(石墨)和增强剂(粉煤灰)在基体(铁)中分布均匀。试样的最大密度为 5.7 克/立方厘米,总体密度为理论密度的 70%。FM03 试样的耐磨性更好,达到 4.7 × 10-8 g/Nm,最佳摩擦系数为 0.4。传统摩擦材料的比磨损率比 FM03 试样高 97.7%。
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引用次数: 0
Coupled CFD-DEM with Flow and Heat Transfer to Investigate the Melting and Motion of Alloy 用流动和传热耦合 CFD-DEM 研究合金的熔化和运动
Pub Date : 2024-09-16 DOI: 10.1007/s11663-024-03274-0
Yong Liu, Shusen Cheng, Wenxuan Xu

The melting and motion of ferroalloys play a crucial role in the mass transfer and homogenization of molten steel in ladles. Heat transfer, melting, and solidification behavior of an alloy affect its size, thereby altering its motion within the gas-stirring ladle. This study established a heat transfer and solidification-melting model for alloy particles in high-temperature metal liquids. The computational fluid dynamics (CFD) method was used to simulate the fluid within the ladle, and the discrete element method (DEM) was employed for the alloy particles. This coupling approach elucidates the motion trajectories of different types of alloys in molten steel under flow and heat exchange, particle heating, melting, and shrinkage conditions. Furthermore, the effects of alloy size, initial alloy temperature, molten steel flow rate, and molten steel temperature on the melting behavior of different types of alloys were investigated. The results showed that the melting time exponentially increased with increasing alloy size or decreasing molten steel flow rate. Moreover, the alloy melting time decreased with increasing initial alloy temperature or molten steel temperature. The impact of these factors on the melting of FeCr, FeMn, FeSi, and Al alloys was also evaluated. Furthermore, FeSi and Al alloys added at different positions in the ladle with symmetric dual gas bottom blowing had a residence time of only 1 second in the molten steel and did not completely melt. These findings indicate that FeSi, Al, and FeCr alloys should be added at the 0.4R position in the symmetrical plane. Furthermore, the − 0.4R or − 0.2R positions are more favorable for the melting of FeMn.

铁合金的熔化和运动对钢包中钢水的传质和均匀化起着至关重要的作用。合金的传热、熔化和凝固行为会影响其尺寸,从而改变其在气体搅拌钢包内的运动。本研究建立了合金颗粒在高温金属液体中的传热和凝固-熔化模型。计算流体动力学(CFD)方法用于模拟钢包内的流体,离散元素法(DEM)用于模拟合金颗粒。这种耦合方法阐明了钢水中不同类型合金在流动和热交换、颗粒加热、熔化和收缩条件下的运动轨迹。此外,还研究了合金尺寸、合金初始温度、钢水流速和钢水温度对不同类型合金熔化行为的影响。结果表明,随着合金尺寸的增大或钢水流速的减小,熔化时间呈指数增长。此外,合金熔化时间随着合金初始温度或钢水温度的升高而缩短。还评估了这些因素对 FeCr、FeMn、FeSi 和 Al 合金熔化的影响。此外,在钢包中不同位置加入的 FeSi 和 Al 合金在钢水中的停留时间仅为 1 秒,并且没有完全熔化。这些发现表明,铁硅、铝和铁铬合金应添加在对称面的 0.4R 位置。此外,- 0.4R 或 - 0.2R 位置更有利于铁锰的熔化。
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引用次数: 0
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Metallurgical and Materials Transactions B
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