锰铁矿的绿色还原浸出和 Mn3O4 纳米粒子的生产:动力学模型和各种还原剂的比较

IF 5.5 3区 工程技术 Q1 ENGINEERING, CHEMICAL Journal of the Taiwan Institute of Chemical Engineers Pub Date : 2024-04-04 DOI:10.1016/j.jtice.2024.105479
Milad Karimi , Saeid Karimi , Ersin Yener Yazici
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引用次数: 0

摘要

背景确保关键金属的安全对于从化石燃料向可再生能源过渡至关重要。在这方面,从各种来源和低品位矿石中提取金属可以实现金属的可持续生产。本研究使用了草酸、柠檬酸、抗坏血酸、醋酸、单宁酸、过氧化氢、硫酸铁(II)、硫代硫酸钠和 DL-苹果酸等多种还原剂,对含锰铁矿石浸出的可行性进行了评估和比较。重要发现选择 DL-苹果酸作为研究其他因素的主要还原剂,是因为它具有新颖性(作为还原剂)、生态友好性、成本效益高、易获取和易储存等特点。因此,考虑到不同的温度水平、粒度、酸浓度和浸出时间,对以 DL-苹果酸为还原剂的锰铁矿石溶解进行了更详细的研究。将温度从 298 K 提高到 348 K 显著提高了浸出回收率,从 27.00 % 提高到 70.11 %。据观察,将矿石粒度从 -212 μm 减小到 -38 μm,可将浸出回收率从 57.74% 提高到 70.11%。此外,与不含还原剂的培养基中仅有 5.32 % 的沥滤回收率相比,仅添加 250 % 的 DL-苹果酸可显著提高沥滤回收率至 70.11 %。值得注意的是,硫酸的浓度对浸出回收率有直接影响,浓度为 0.5 M 时,浸出回收率提高了 28.28%;浓度为 4 M 时,浸出回收率提高了 93.08%。计算得出的活化能约为 33 kJ/mole,这证实了混合机制控制了反应。Mn3O4 纳米粒子是利用孕浸溶液(PLS)并通过多级共沉淀法合成的。在该方法中,过氧化氢被用来改变氢氧化锰相,与其他热处理方法相比,这是一种更环保的方法。扫描电子显微镜(SEM)和电离氧化物显微镜(EDX)分析表明,锰的平均粒径为 80 纳米,呈球形,无杂质。合成纳米粒子的 XRD 图谱证实了 Mn3O4 相的组成。
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The green reductive leaching of manganiferous iron ore and Mn3O4 nanoparticles production: Kinetic modeling and comparison of various reductants

Background

Securing critical metals is crucial for the transition from fossil fuels to renewable energies. In this regard, extracting metals from various sources and low-grade ores can lead to the sustainable production of metals. Manganese, as a strategic metal, can play a significant role in achieving this goal.

Methods

In this study, various reductants such as oxalic acid, citric acid, ascorbic acid, acetic acid, tannic acid, hydrogen peroxide, iron (II) sulfate, sodium thiosulfate, and DL-malic acid were used to evaluate the feasibility and comparison on the manganiferous iron ore leaching.

Significant findings

DL-malic acid was chosen as the main reductant to investigate other factors because it is novel (as a reductant), eco-friendly, cost-effective, accessible, and easily storable. Therefore, more detailed studies on the dissolution of manganiferous iron ore in the presence of DL-malic acid as the reductant were carried out considering different levels of temperature, particle size, acid concentrations, and leaching time. Increasing the temperature from 298 K to 348 K notably boosted the leaching recovery from 27.00 % to 70.11 %. It was observed that decreasing the ore particle size from -212 μm to -38 μm resulted in an enhancement of leaching recovery from 57.74 % to 70.11 %. Also, adding only 250 % stoichiometry of DL-malic acid notably increased the leaching recovery to 70.11 %, compared to just 5.32 % in a reductant-free medium. It should be noted that the concentration of sulfuric acid had a direct impact on leaching recovery, increasing by 28.28 % with a concentration of 0.5 M and by 93.08 % with a concentration of 4 M. In this research work, the kinetic of the leaching process was modeled using the modified shrinking core model (MSCM). The calculated activation energy was about 33 kJ/mole, which confirmed that the mixed mechanism controlled the reaction. Mn3O4 nanoparticles were synthesized using a pregnant leach solution (PLS) and through a multi-stage co-precipitation method. In this method, hydrogen peroxide was used to modify the manganese hydroxide phase as a more eco-friendly method than other heat treatment methods. The SEM and EDX analyses revealed an average particle size of 80 nm with spherical shapes and no impurities. The XRD pattern of the synthesized nanoparticles confirmed the Mn3O4 phase composition.

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来源期刊
CiteScore
9.10
自引率
14.00%
发文量
362
审稿时长
35 days
期刊介绍: Journal of the Taiwan Institute of Chemical Engineers (formerly known as Journal of the Chinese Institute of Chemical Engineers) publishes original works, from fundamental principles to practical applications, in the broad field of chemical engineering with special focus on three aspects: Chemical and Biomolecular Science and Technology, Energy and Environmental Science and Technology, and Materials Science and Technology. Authors should choose for their manuscript an appropriate aspect section and a few related classifications when submitting to the journal online.
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