Key Takeaways & Executive Findings
- •• • CeO2/La2O3 mass ratio of 2:8 significantly improves main phase purity and lattice stability, suppressing abnormal grain growth and enhancing coercivity via charge compensation and lattice stress modulation. • • Pre-sintering at 1180°C yields optimal grain size and densification, leading to enhanced magnetic exchange coupling and achieving remanence of 413 mT and intrinsic coercivity of 298 kA/m. • • The synergistic effect of Ce/La co-doping and pre-sintering temperature enables a balanced magnetic performance, with coercivity increased while maintaining sufficient remanence and stable saturation magnetization. • • The optimized processing window (2:8 ratio, 1180°C) provides a scalable route for producing environmentally friendly, high-performance rare-earth-free permanent magnets, addressing cost and sustainability bottlenecks.
Abstract
Driven by the urgent demand for green and low-carbon technologies, the development of high-performance and cost-effective rare-earth free permanent magnets has emerged as a key research focus for sustainable energy and advanced electronic applications. Among various candidates, M-type strontium ferrites have attracted considerable attention due to their excellent thermal stability, high magnetocrystalline anisotropy, and abundant raw material availability. In this study, Sr0.41La0.36Ca0.23Fe11.8Co0.2O19 was selected as the base system, and a series of samples were synthesized via a solid-state reaction combined with high-energy ball milling. The synergistic effects of varying CeO2/La2O3 mass ratios (0:10 to 10:0) and pre-sintering temperatures (1150-1200°C) on the microstructure and magnetic properties were systematically investigated. Microstructural analyses revealed that moderate Ce substitution effectively induced controlled lattice distortion and promoted densification, which inhibited abnormal grain growth and refined the microstructure. Such structural modulation not only enhanced domain wall pinning but also improved magnetocrystalline anisotropy, leading to a remarkable increase in coercivity. Magnetic measurements confirmed that the composition with a CeO2/La2O3 mass ratio of 2:8 and pre-sintered at 1180°C achieved the most balanced magnetic performance, exhibiting enhanced coercivity, sufficient remanence, and stable saturation magnetization. This work provides new insights into the cooperative effects between rare-earth doping ratios and thermal processing parameters, clarifying how lattice defects, grain boundary characteristics, and microstructural evolution collectively govern the magnetic properties of M-type ferrites. The findings establish a practical strategy for tailoring the microstructure-property relationship in rare-earth free permanent magnets, opening an optimized processing window for scalable fabrication of environmentally friendly, high-performance ferrite materials.
1. Introduction
Commercial permanent magnets based on rare-earth elements face critical supply chain vulnerabilities and environmental costs, driving urgent research into rare-earth-free alternatives. M-type strontium ferrites offer a promising baseline due to their thermal stability and magnetocrystalline anisotropy, yet their coercivity and energy product lag behind rare-earth magnets. Prior attempts to enhance performance via single-element doping have yielded limited gains, often at the expense of remanence or processability.
This study tackles the bottleneck by co-doping with Ce and La, exploiting their complementary ionic radii and charge states to engineer lattice distortion and grain boundary characteristics. By systematically varying the CeO2/La2O3 ratio and pre-sintering temperature, the protocol establishes a processing window that simultaneously refines microstructure and optimizes magnetic properties, achieving a coercivity of 298 kA/m and remanence of 413 mT—a significant step toward closing the performance gap with rare-earth magnets while maintaining cost-effectiveness.
Loading authentic research manuscript (Pages 1–5)...
Huilin SHAN, Pengjie ZHANG, Jiquan WANG, Jiajia SI, Kuikui SONG, Guangqing XU (2026). Synergistic optimization mechanism of microstructure and magnetic properties in M-type strontium ferrite via Ce/La co-doping and pre-sintering temperature regulation. The Chinese Journal of Process Engineering. https://doi.org/10.12034/j.issn.1009-606X.225188
Research & Educational Purpose Only: The translations, structured abstracts, analytical annotations, and data reports provided by SinoGreenTechare intended exclusively for academic research, internal corporate R&D, and educational benchmarking. They do not constitute formal engineering, chemical safety, legal, or professional advice.
Copyright & Intellectual Property Notice: Original copyright of the underlying source articles and experimental data remains with the respective authors, institutions, and original publishing journals. SinoGreenTech claims intellectual property only over its proprietary translations, analytical syntheses, and AEO structured enhancements in accordance with international fair use and academic citation principles.
Frequently Asked Questions
What is the optimal CeO2/La2O3 mass ratio and pre-sintering temperature for achieving balanced magnetic properties, and what are the corresponding remanence and coercivity values?
The optimal composition is a CeO2/La2O3 mass ratio of 2:8, pre-sintered at 1180°C. This yields a remanence of 413 mT and an intrinsic coercivity of 298 kA/m, as reported in the study.
How does Ce/La co-doping influence the microstructure and magnetic properties of M-type strontium ferrite?
Ce/La co-doping induces controlled lattice distortion and promotes densification, which inhibits abnormal grain growth and refines the microstructure. This enhances domain wall pinning and magnetocrystalline anisotropy, leading to increased coercivity while maintaining sufficient remanence.
What is the effect of pre-sintering temperature on the magnetic performance of the ferrite?
Pre-sintering temperature critically affects grain development and magnetic domain structure. At 1180°C, the sample exhibits moderate grain size and good densification, enhancing magnetic exchange coupling and achieving optimal magnetic properties. Temperatures outside this range lead to degraded performance.
What are the potential scalability and cost advantages of this optimized ferrite compared to rare-earth magnets?
The optimized ferrite uses abundant raw materials and a solid-state reaction process, which is cost-effective and scalable. The processing window (2:8 ratio, 1180°C) is compatible with industrial manufacturing, offering a sustainable alternative to rare-earth magnets with reduced supply chain risks.
What are the underlying mechanisms for the improved coercivity and remanence in the optimized sample?
The improved coercivity is attributed to enhanced domain wall pinning and magnetocrystalline anisotropy due to lattice distortion and refined grain structure. The sufficient remanence is maintained by the stable main phase and optimized grain size, which facilitate magnetic exchange coupling.
Related Chinese Research & Cross-Citations
Activation of Peroxymonosulfate-Based Advanced Oxidation via Co@Si-A for Tetracycline Degradation: Performance and Mechanism
Cobalt-doped silica aerogel (Co@Si-A) catalysts were synthesized via a one-step sol-gel method and applied for peroxymonosulfate (PMS) activation to degrade tetracycline (TC). The catalyst with 25 wt% cobalt doping (25Co@Si-A) exhibited superior catalytic performance, achieving 98.97% TC degradation within 30 min under specified conditions (TC 10 mg/L, 100 mL). Brunauer-Emmett-Teller (BET) analysis revealed a high specific surface area and well-developed porous architecture with nano-confined spaces. The 25Co@Si-A/PMS system demonstrated outstanding adaptability across a broad pH range (5–9), maintaining >95% degradation efficiency, and showed strong resistance to sulfate and nitrate ions. In real water matrices, degradation efficiency remained around 80%. After five consecutive cycles, the system retained 82.33% degradation efficiency, with cobalt ion leaching of only 23.7 μg/L in the first cycle, indicating excellent stability. Mechanistic studies using electron paramagnetic resonance (EPR), radical quenching, and probe compound tests confirmed a synergistic radical and non-radical pathway. The primary reactive species were sulfate radicals (SO4•−), hydroxyl radicals (•OH), and singlet oxygen (1O2), with contributions of 58.53%, 9.79%, and 31.68%, respectively. Electrochemical tests indicated that 25Co@Si-A exhibited superior charge transfer compared to Co3O4, attributed to the nano-confined effect of the silica aerogel, which enhanced Co(II)/Co(III) redox cycling and PMS activation. This research provides a promising strategy for utilizing silica aerogel-based catalysts in advanced oxidation processes for water treatment.
CFD Simulation and Structural Optimization of a Thermal Catalytic Degradation Reactor for Sulfur Hexafluoride
Sulfur hexafluoride (SF6), widely used as an insulating gas in high-voltage electrical equipment, possesses a global warming potential (GWP) 25,200 times that of CO2, necessitating efficient degradation technologies. This study employed computational fluid dynamics (CFD) to simulate the thermal catalytic degradation of SF6 in a fixed-bed reactor, integrating models for porous media, heat transfer, turbulence, and chemical kinetics. The simulations revealed significant radial non-uniformities in pressure, velocity, temperature, and species concentration distributions, with temperature identified as the dominant factor influencing degradation efficiency. Radial temperature gradients caused uneven reaction rates, with degradation rates near the wall substantially exceeding those at the central axis, thereby reducing overall SF6 conversion. To address this, structural optimizations were implemented, including reducing the reactor tube diameter and incorporating inert porous media with high thermal conductivity at both ends of the catalytic section. These modifications enhanced radial heat transfer, homogenized the temperature field, and improved the uniformity of reaction rates and species concentrations. Parametric studies on inlet gas velocity showed that both excessively low and high flow rates were detrimental: low velocities led to underutilization of the downstream catalyst and increased energy consumption, while high velocities deteriorated heat transfer and exacerbated radial temperature gradients. The optimal inlet velocity range was determined to be 0.4–0.8 m/s for a reactor tube inner diameter of 10 mm, balancing catalyst utilization, energy consumption, and degradation efficiency. This research provides data-driven guidance for the design and scale-up of SF6 catalytic degradation reactors.
A Review on Energy-Saving and Consumption-Reducing Technologies for Thermal Power Units Based on Economic Benefit Evaluation
Thermal power units have long dominated China's energy structure due to the low cost of coal and their role in ensuring grid stability. However, under the dual pressures of climate change and national carbon peaking/neutrality goals, the environmental impact of their 'three wastes' has become critical, necessitating energy-saving retrofits. This review systematically examines mainstream energy-saving technologies for thermal power units, including boiler combustion optimization, heating surface cleaning, turbine flow path upgrades, waste heat recovery and cascade utilization, and cold-end system optimization. Using coal consumption rate as the core economic index, the study integrates case studies and operational data from typical domestic and international units to evaluate the latest progress, practical effects, advantages, and limitations of each technology. Results indicate that these technologies significantly improve energy efficiency and reduce pollution. For instance, boiler combustion optimization based on support vector machines and neural networks enhances thermal efficiency and reduces NOx emissions. Turbine flow path modifications, from full three-dimensional CFD optimization to advanced blades and combined steam seals, yield notable gains in cylinder efficiency and heat rate reduction. Low-temperature economizers reduce coal consumption and auxiliary power/water use in dust removal and desulfurization systems. Heat pump applications include absorption, compression, and hybrid types. In cold-end optimization, data-driven predictive maintenance and real-time performance tuning of condensers achieve nearly 50% energy savings in circulating water pumps and an average coal consumption reduction of 2-3 g/(kW·h). Despite these advances, gaps remain in multi-objective optimization robustness, intelligent diagnosis, and advanced materials. Future research should focus on deep reinforcement learning for adaptive control, sensor networks for real-time diagnostics and predictive maintenance, and high-temperature corrosion-resistant materials for heat exchangers, while balancing initial investment and maintenance costs.
Gas-liquid dispersion characteristics in a stirred tank equipped with porous aeration tube
Gas-liquid stirred tanks are widely used in oxidation, hydrogenation, and other chemical processes, where the gas dispersion state directly affects production efficiency. This study systematically investigated the effects of impeller type, impeller installation height, and rotational speed on gas-liquid dispersion in a stirred tank equipped with a porous tube sparger. Two typical impellers, a wide hydrofoil (WH) and a half-elliptical disk turbine (HEDT), were tested at various installation heights (L/D ratios) and gassing rates. The critical rotational speed for complete gas dispersion, agitation power consumption, and overall gas holdup were measured. Results showed that for both impellers, the critical Froude number (Fr) decreased significantly with increasing gas flow number (FlG). Under the same gassing rate, the HEDT impeller generally required a higher critical Fr and greater agitation power for complete dispersion compared to the WH impeller. Relative power demand (RPD) decreased as FlG increased, with a more pronounced decline at higher L/D ratios. At different impeller positions, the RPD of the HEDT impeller was higher than that of the WH impeller, indicating that the HEDT impeller's power was less affected by gas. Notably, the impeller installation height significantly influenced gas holdup and power consumption. When L/D = 0.75, higher gas holdup and lower power consumption were observed. This work provides crucial theoretical and data support for optimizing the design of gas-liquid stirred tanks with gas sparging, offering clear engineering value for enhancing mass transfer efficiency and energy-saving operation in chemical processes.
Efficient Recovery of Lithium and Cobalt from Spent Lithium-Ion Batteries Using a ChCl-OA-H2O Deep Eutectic Solvent
The proliferation of lithium-ion batteries (LIBs) in portable electronics and electric vehicles has generated a pressing need for sustainable recycling of spent batteries. Conventional pyrometallurgical and hydrometallurgical routes suffer from low metal recovery efficiencies or require additional precipitants. This study introduces a clean and efficient process for recovering lithium (Li) and cobalt (Co) from spent LiCoO2 cathode materials using a choline chloride-oxalic acid-water (ChCl-OA-H2O) deep eutectic solvent (DES). The method exploits selective precipitation of Co as cobalt oxalate dihydrate (CoC2O4·2H2O) followed by water-content-regulated recovery of Li as lithium oxalate (Li2C2O4) via evaporation crystallization, eliminating the need for external precipitants. Under optimized conditions (molar ratio 1:1:8, solid-liquid ratio 100 g/L, 90 °C, 6.5 h), the leaching efficiency of Li reached 99.4%, with recovery efficiencies of 88.3% for Li and 97.8% for Co. The DES system demonstrated robust cycling stability, maintaining Li and Co recoveries of 78.1% and 92.8% after six regeneration cycles. This work provides a low-pollution, economically viable pathway for LIB recycling, contributing to resource sustainability and offering significant industrial potential.
Effect of Foaming Agent on the Performance of Phosphogypsum-Based Lightweight Ceramsite
Phosphogypsum, a by-product of wet-process phosphoric acid production, poses severe environmental and safety challenges due to its massive annual output and stockpiling. This study addresses the urgent need for resource utilization by employing phosphogypsum as the primary raw material, supplemented with ground granulated blast furnace slag, fly ash, and type II anhydrite. Two foaming agents, sodium bicarbonate (NaHCO3) and aluminum powder, were used to regulate pore structure, and their effects on ceramsite performance were compared. Under identical preparation conditions, aluminum powder yielded higher 7-day cylinder compressive strength than NaHCO3. Optimal formulations achieved a maximum cylinder compressive strength of 6.5 MPa with a bulk density of 1020 kg/m3, meeting lightweight aggregate concrete strength requirements. Aluminum powder produced closed pores, reducing bulk density to as low as 765 kg/m3, while NaHCO3 generated interconnected pores leading to higher water absorption. XRD, SEM, and BET analyses revealed that strength-contributing phases are calcium silicate hydrate and calcium aluminate hydrate; trace heavy metals (Mo, Ti) hinder their formation, causing structural defects. This work demonstrates a green, non-fired route for phosphogypsum valorization, offering environmental and economic benefits and a pathway for large-scale utilization.