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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Al/Zr synergetic modification tailored low-cobalt single crystal LiNi0.72Co0.05Mn0.23O2 cathode for high-performance lithium-ion battery

Hua Yan,Yu-hong Luo,Ying Lei,Qing-lin Pan,Jun-chao Zheng

N ickle (Ni)-rich layered oxides as promising candidate of high-capacity cathode materials have aroused extensive concern primarily regarding their higher specific capacity. However, the major hurdle of Ni-rich cathodes (Ni content ≥0.7) is their poor cycling stability, which often suffers from the release of oxygen, structural degradation and increased impedance during cycling, especially at high voltage or high temperature. Herein, we demonstrated a feasible solid phase method for easy industrialization based on the Al 3+ /Zr 4+ co-doping in LiNi 0.72 Co 0.05 Mn 0.23 O 2 (A X Z Y -NCM) single-crystal cathode. The optimized A 0.5 Z 0.5 -NCM single-crystal material exhibited greatly enhanced structural and thermal stability. XRD refinement results indicated that both Al 3+ and Zr 4+ were mainly located in transition metal (TM) sites, strengthening the layered structure through strong M-O bonds and inhibiting cation mixing. In-situ XRD revealed that the synergistic rivet effect of Al/Zr co-doping alleviates anisotropic lattice stress-strain during charge/discharge process. Accordingly, the A 0.5 Z 0.5 -NCM cathode can output a high initial capacity of 177.3 mAh g −1 at 1 C, and captured a more desirable capacity retention of 85.10 % than that of U-NCM (74.33 %) at 1 C over 200 cycles. Even at a high voltage of 4.5 V, its capacity retention can still reach 82.37 %, significantly surpassing the unmodified U-NCM (31.0 %). The above results demonstrated that well-designed dual doping is highly effective for strengthen structure stability and cycling performance of Ni-rich cathodes.

CAS / MDL: 1310-66-3 1314-23-4
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Journal of Cleaner Production · 2024 · IF 9.7

Precise fabrication of Ti2O from TiO2 by Al reduction towards potentially lower-cost Ti metal powder production

Taotao Cai,Ying Zhang,Shili Zheng,Peiyi Yan,Yi Zhang

Titanium is a highly valued material. Developing a lower-cost titanium (Ti) metal powder production process, potentially substituting the conventional Kroll-HDH method, has challenged the titanium community for decades. The ease of aluminum forming alloys with titanium and the strong chemical affinity of titanium to oxygen rule out the possibility of fabricating pure Ti metal directly by aluminum reduction of TiO 2 . Based on the demonstrated enhanced deoxidation of Ti using Mg metal, this paper proposes an Al–Mg combined stepwise reduction of TiO 2 to fabricate Ti metal powder. Critical challenges overcome in this research include predicting reaction thermodynamics and preparing Ti 2 O intermediate by Al reduction of TiO 2 without significant Al alloying, which is made possible by forming mild-acid soluble Ca 12 Al 14 O 32 Cl 2 byproduct. Various Al reduction conditions were investigated and optimized. To the best of our knowledge, it is the first report to fabricate Ti 2 O powder by Al reduction of TiO 2 with a highly stable chemical composition. The difficulty of sintering the Ti 2 O intermediate before Mg deoxidation to reduce the surface oxygen contribution is mitigated by mixing a certain amount of low-oxygen titanium powder with the Ti 2 O powder. This allows the densification temperature to be lowered from 1400 °C for sintering pure Ti 2 O powder to 1100 °C. Even with as much as around 15 wt% oxygen, the sintered powder can be effectively deoxidized by Mg with the help of hydrogen. A titanium metal powder with an oxygen content of 0.134 wt%, an Al content of 0.123 wt%, and other impurities meeting the standard of pure titanium metal powder (GB/T 34486-2017 FTA1) is successfully prepared by the Al reduction-Mg deoxidation combined process. It is a promising alternative for producing titanium metal powder and its derivatives.

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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Precisely regulating combustion and ectrostatic discharge safety properties of Al/CuO nanothermite by inserting g-C3N4 nanosheet

Chong Wan,Yushu Xiong,Honghong Qin,Zhao Qin,Suhang Chen,Kangzhen Xu

Nanothermites are presenting competitive advantage potential in military and civilian applications, but high electrostatic discharge (ESD) sensitivity severely hinders their preparation, storage and usage. Aiming to improve the safety and combustion properties of energetic materials (EMs), the two-dimensional semiconductor materials graphite carbon nitride (g-C 3 N 4 also abbreviated as CN) was inserted into the Al/CuO mixture via the one-step sol-freeze-drying method. The successful preparation of samples was confirmed by morphological and chemical bond characterization. Then DFT calculation and BET tests prove that more active sites exist in reaction interface, and the adsorption between Al atoms and CuO unit cells are easier due to polyvinylpyrrolidone (PVP) and g-C 3 N 4 functioning, thereby improving the combustion of Al/CuO and ESD safety. The Al/CuO/CN nanocomposite with 2.5 wt% CN has an ESD ignition threshold of 3.2 mJ and realizes maximal reaction energy and constant volume heat of combustion ( Q v ) of 1400.4 J·g −1 and 5896 J·g −1 , respectively. As the CN content grows to 10.0 wt%, the ESD ignition threshold keeps decreasing to 8.45 mJ. Additionally, PVP and CN show superior advantages in regulating the combustion of Al/CuO, and the possible effect mechanism is investigated. This work will provide a fresh strategy for extending applications of nanothermites.

CAS / MDL: 1317-38-0 7429-90-5
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Materials Research Letters · 2024 · IF 8.6

Macro- and meso-mechanic investigations on the mechanical properties of heterostructured Al matrix composites featuring intragranular reinforcement

Yang Zhao,Xiaobin Lin,Xudong Rong,Xiang Zhang,Dongdong Zhao,Chunnian He,Naiqin Zhao

Aluminum matrix composites (AMCs) reinforced with intragranular nano-sized Al2O3 were used as model material to investigate the effects of intragranular nano reinforcement on the mechanical properties at macro- and meso- levels. The results revealed that intragranular Al2O3 effectively facilitates the dislocation multiplication, which in turn enables the grain interior to endure high levels of plastic strain and consequently alleviates stress concentration at the grain boundary. Furthermore, intragranular Al2O3 leads to a collective enhancement in the intrinsic mechanical properties across domains of varying sizes, thereby contributing to the coordinated plastic deformation of heterogeneous grains, and enhancing the creep resistance of composite.

CAS / MDL: 1317-38-0
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2024 · IF 5.8

Microstructure, mechanical and friction-wear properties of SiC-WC composite with Al and C as sintering aids

Zhouxi Tan,Mingkang Zhang,Shuai Zhao,Yihua Huang,Zhengren Huang

Low strength and poor performance of SiC–WC composite for seals, attributable to the use of a large amount of liquid phase sintering additives, limit the application prospects of these materials. This study focuses on preparing high-strength, high-toughness, and wear-resistant SiC–WC composite using a small amount of aluminum and carbon black as sintering additives. The results revealed that the specimen containing 50 wt% WC exhibited the maximum flexural strength and fracture toughness of 645.9 MPa and 7.49 Mpa m 1/2 , respectively. These improvements were attributed to the deoxidizing and solid-solution effects of Al and the reinforcing effect of the WC second phase. Moreover, the specific wear rate was measured at 8.06 × 10 −7 mm 3 N −1 m −1 , which was 56.9 % lower than that of monolithic SiC. Results from Raman spectral analysis provided evidence of the presence of W–O bonds on the wear surface, indicating that the SiO 2 film could be successfully replaced by a WO 3 film.

CAS / MDL: 7429-90-5
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Coatings · 2024 ·Vol. 14 ·期 9 ·1082 · IF 2.9

Preparation and Properties of Conductive Aluminum Powder (Al@Si@C) for Water-Borne Heavy-Duty Anticorrosive Coatings

Qingpeng Li,Jiaxing Liu,Tiancheng Jiang,Xiaoyun An,Na Wang,Zhixiu Xu,Wanyuan Guo,Liang Zhang,Xiaofeng Liu

To improve the storage stability and conductivity of aluminum powder in an aqueous environment, the surface of aluminum powder was treated to form silica film by the sol–gel method, then was treated with conductive modification to introduce nanocarbon black particles so that conductive aluminum powder could be prepared to solve the application bottleneck of aluminum powder in water-borne heavy-duty anticorrosive coatings. The structure, surface morphology, and composition of the modified aluminum powder were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), X-ray photoelectron spectroscopy (XPS), and X-ray powder diffraction (XRD). The corrosion resistance and electrochemical properties were measured using a hydrogen evolution test and an 2electrochemical test. The results showed that there was a compact SiO2film formed on the surface of the prepared conductive aluminum powder, and the conductive filler nanocarbon black was uniformly grafted on the surface. According to the hydrogen evolution test at 100 h/50 °C, conductive aluminum powder with 5 wt% carbon black exhibited the best hydrogen evolution effect, with a hydrogen evolution amount of only 0.5 mL. The prepared conductive aluminum powder was applied to the water-borne coatings, and the storage stability test, electrochemical polarization test, and neutral salt spray test were further conducted. The water-borne coatings prepared with conductive aluminum powder still showed good performance and had no reaction after 6 months of storage. Compared with the coating containing SiO2-modified aluminum powder, the coating exhibited better corrosion resistance.

CAS / MDL: 111-76-2 102-71-6
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FUEL · 2025 · IF 7.5

Synergistic effect of hollow n-Al/H-MoO3 in the gas-phase reaction zone of solid propellant

Shuping Li,Cheng Dong,Xuan Qi,Shiyong Chen,Lixiao Shen,Yinning Zeng,Yan Li,Zhenxin Yi,Lin Zhang,Shunguan Zhu

A novel hollow-structured thermite, n-Al/H-MoO 3 , is designed to enhance the energy release mode and combustion performance of solid propellant. This research comprehensively explores the preparation and structural features of n-Al/H-MoO 3 within solid propellants. Furthermore, a series of rigorous combustion tests, performance assessments, and computational simulations are conducted to investigate its practical application. Experimental results indicate that the significant improvements in combustion performance have been observed by integrating this innovation n-Al/H-MoO 3 in solid propellants as a burning rate modifier. The heat of explosion increases to 6135 J·g −1 , a 41.76 % increase over the blank group (M0). Furthermore, its flame temperature is 494.3°C higher than that of the blank group. These substantial gains are primarily attributed to the unique hollow structure of n-Al/H-MoO 3 , which facilitates the reaction between H-MoO 3 and Al in the gaseous phase region, thereby improving combustion dynamics. The research findings offer theoretical foundations and experimental support for the design of more efficient and stable propellants.

CAS / MDL: 2432-87-3 4098-71-9
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Journal of Energy Chemistry · 2025 · IF 14.9

On-site hydrolytic H2 production by CaH2/(Al/Si) composites via Na+ bridging effect for fuel cell

Ali Hammad,Siyi Zou,Fandi Ning,Ghulam Nabi,Yuzhuo Jiang,Bin Tian,Wentao Huang,Muhammad Rashid,Shiqi Zhao,Xiaochun Zhou

Inorganic materials can solve transportable and on-site hydrolytic hydrogen generation issues. CaH 2 /(Al/Si) composites are preferable due to their notable chemical properties. However, these composites require pretreatments, an inert environment, and long hours of physical ball milling for high homogeneity and synergistic effects. CaH 2 also inhibits the hydrolysis reaction by forming its products on the Al/Si surface, which hinders the direct utilization of composites. This work represents the first investigation of NaH-CaH 2 (Al/Si) fuel composites, which greatly overcome these limitations and can be directly used for on-site hydrogen generation and proton exchange membrane (PEM) fuel cells. The NaH-CaH 2 (Al/Si) fuel composites were prepared by using a straightforward mixing method with variable composition ratios, showing high H 2 yield and fuel cell (FC) performance. NaH addition provides the bridge effect, which opens up a new way to enable efficient hydrolysis and greatly enhances the hydrolysis activity of CaH 2 /(Al/Si) composites. The novel fuel composites (NaH-CaH 2 /Al) have extraordinary FC performance and a 0.42 W/cm 2 peak power density greater than commercial hydrogen generators. It provides high H 2 yield 84.4 % for NaH-CaH 2 /Al and 82 % for NaH-CaH 2 /Si compared to NaOH-CaH 2 (Al/Si), NaCl-CaH 2 (Al/Si), and KCl-CaH 2 (Al/Si) composites. The NaH bridge effect hinders the direct water contact and stops the formation of Ca(OH) 2 around Al/Si, which provides adequate pathways for the CaH 2 (Al/Si) hydrolysis. The impressive capabilities of novel fuel composites are anticipated to offer practical uses in fuel cells, automobile applications, and portable/on-board H 2 generation.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Vacuum thermal reduction of used alkaline Zn–Mn batteries to recover Zn and prepare Al–Mn alloys

Boxiong Zhang,Wenxiong Dong,Yaowu Wang,Xiaomeng Cao,Jianping Peng,Yuezhong Di,Buju Guo,Zhongyu An,Jiaoyang Xia

Alkaline zinc–manganese batteries are the most used disposable batteries in the world and cannot be recharged. Spent alkaline zinc–manganese batteries are mainly disposed of in landfills, and the resulting enrichment of the soil with potassium(K), zinc(Zn), and manganese(Mn) pollutes the groundwater and wastes valuable resources. Herein, a process for the treatment of used alkaline zinc(Zn)–manganese(Mn) batteries that involved water leaching, calcination, and vacuum aluminothermic reduction was developed. Investigation of the elemental migration process and reaction mechanism showed that the purity of potassium carbonate(K 2 CO 3 ) reached 99 % with 92.1 % recovery at a water leaching temperature of 60 °C and time of 25 min. The leaching slag was calcined at 700 °C for 1 h to obtain calcined slag with zinc oxide (ZnO), manganese(III) oxide (Mn 2 O 3 ), and manganese(II) oxide (MnO) as the main phases. When the calcined slag was reduced with aluminum powder, the recovery rate of Zn reached 99.7 % at a reduction temperature of 1100 °C, reduction time of 2 h, and ratio of aluminum powder to calcined slag of 1.5:1. Under these conditions, Mn was recovered in the form of Al 6 Mn alloy, and the main phase of the remaining reduced slag was alumina. In this study, potassium and metallic zinc were separated and recovered, and at the same time, an aluminum(Al)–manganese(Mn) alloy was prepared. The developed environmentally friendly and emission-free process enables the efficient recycling of the valuable resources K, Zn, and Mn, resulting in cleaner battery disposal.

CAS / MDL: 1317-34-6 1317-35-7
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Polymers · 2025 ·Vol. 17 ·期 14 ·1994 · IF 4.9

PVP-Regulated Self-Assembly of High-Strength Micrometer-Scale Al/CuO/AP Energetic Microspheres with Enhanced Reactivity

Xuyang Wu,Hongbao Wang,Chenglong Jiao,Benbo Zhao,Shixiong Sun,Yunjun Luo

Al-based nanocomposite energetic materials have broad application prospects in explosives and propellants, owing to their excellent energy release efficiency. However, their insufficient reliability, poor stability, and difficulty of formation limit their practical application. This study employed self-assembly using a hydrophilic polymer polyvinylpyrrolidone (PVP) together with nano-aluminum powder (Al), copper oxide (CuO), and ammonium perchlorate (AP) to obtain high-strength and high-activity composite micrometer-sized microspheres. The influence of PVP concentration on the mechanical behavior of Al/AP composite microspheres was systematically investigated, and Al was replaced with ultrasonically dispersed Al/CuO to explore the mechanism of action of PVP in the system and the catalytic behavior of CuO. PVP significantly enhanced the interfacial bonding strength. The Al/AP/5%PVP microspheres achieved a strength of 8.4 MPa under 40% compressive strain, representing a 365% increase relative to Al/AP. The Al/CuO/AP/5%PVP microspheres achieved a strength of 10.2 MPa, representing a 309% increase relative to Al/CuO. The mechanical properties of the composite microspheres were improved by more than threefold, and their thermal reactivities were also higher. This study provides a new method for the controlled preparation of high-strength, high-activity, micrometer-sized energetic microspheres. These materials are expected to be applied in composite solid propellants to enhance their combustion efficiency.

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Journal of Sustainable Metallurgy · 2025 · IF 3.2

Thermal Evolution and Leaching Activity of Kaolinite and Boehmite, the Key Al-Containing Minerals in Coal Gangue

Shao Shuang,Ma Baozhong,Wang Chengyan,Chen Yongqiang

Extracting Al from coal gangue has the double benefits of realizing the high-value application of coal gangue and mitigating the scarcity of bauxite resource. The key Al-containing minerals in coal gangue include kaolinite and boehmite, and thermal activation is pivotal for stimulating their reactivity. In this study, kaolinite and boehmite were subjected to thermal activation and acid leaching to explore the intrinsic link between their thermal evolution and leaching activity. Results showed that the phase evolution of kaolinite followed a multi-step sequential process in the order of kaolinite → metakaolinite →  γ -Al 2 O 3  → mullite, and Al V in metakaolinite was highly active. For boehmite, it underwent the transformation of boehmite →  γ -Al 2 O 3  →  δ -Al 2 O 3  →  θ -Al 2 O 3 and α -Al 2 O 3 successively. Their reactivity in descending order was γ -Al 2 O 3  >  δ -Al 2 O 3  > boehmite >  α -Al 2 O 3 . Furthermore, a comparative study of leaching temperature demonstrated that elevated temperature favorably strengthened the thermodynamic driving force and greatly promoted the Al extraction. This study is of some theoretical significance for guiding the thermal activation and acid leaching of coal gangue. Graphical

CAS / MDL: 1318-23-6
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ACS Applied Energy Materials · 2025 · IF 5.5

Realization of Reliable Connection of Mg Anode and Al Tab by Ultrasonic Welding for Reachable Magnesium Batteries

Xuxi Teng,Yingying Sun,Jili Yue,Rong Li,Guangsheng Huang,Jingfeng Wang,Chaohe Xu

Rechargeable magnesium batteries (RMBs) have garnered significant attention in recent years. However, the commercialization of RMBs has been severely hampered by the low-strength and high-resistance connections between the magnesium (Mg) anodes and aluminum (Al) tabs. To address this challenge, we perform orthogonal experiments on 0.2 mm-thick Al–Mg ultrasonic welded joints to establish an optimized parameter range. Analysis of variance revealed that ultrasonic amplitude exerted the most dominant influence on joint strength (52.03%), followed by welding time (25.59%) and welding pressure (22.37%), with a significant interaction effect observed between welding time and amplitude. Notably, at a welding pressure of 0.40 MPa, the Al–Mg joint achieved peak performance, including the maximum lap-shear load (59.20 N) and minimal electrical resistance (0.483 mΩ). RMB pouch cells assembled with good-welded tabs demonstrated superior electrochemical performance compared to under and overwelded counterparts, exhibiting reduced internal resistance (3.55 Ω in the first cycle), enhanced capacity retention (77.45% after 60 cycles), and raised Coulombic efficiency (99.88% after 440 cycles).

CAS / MDL: 13463-67-7 872-50-4
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