Facet-dependent growth and dissolution of hematite resulting from autocatalytic interactions with Fe(ii) and oxalic acid†

IF 5.1 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Environmental Science: Nano Pub Date : 2025-01-24 DOI:10.1039/D4EN01004C
Sandra D. Taylor, John B. Cliff, Thomas W. Wietsma and Kevin M. Rosso
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Abstract

The ability to simultaneously monitor the flux of iron atoms within the solution and solid phases can provide considerable insight into mechanisms of iron oxide mineral transformations. The autocatalytic interaction between hematite and Fe(II)-oxalate has long been of interest for its environmental and industrial relevance. In this study we take advantage of iron isotopic labelling and mass-sensitive imaging at the single particle scale to determine how changes in solution composition correlate with the morphologic evolution of faceted, micrometer-sized hematite platelets. Net dissolution is confirmed through analyses of aqueous iron chemistry, as well as by quantitative atomic force microscopy. Isotopic mapping techniques show that Fe(II) readily adsorbs to (001) and (012) surfaces in the absence of oxalate, but when oxalate is present selective dissolution of the (001) surface prevails and Fe deposition via recrystallization is not observed. Comparison between particle microtopographies following reaction with Fe(II), oxalate, and Fe(II)-oxalate show substantially different behaviors, consistent with distinct mechanisms of interaction with hematite surfaces. The extensive characterization conducted on the coupled solution/solid dynamics in this system provides new insight for distinguishing crystal growth, dissolution, and recrystallization processes.

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赤铁矿与铁(II)和草酸的自催化作用导致的面依赖性生长和溶解
同时监测溶液和固相中铁原子通量的能力可以为氧化铁矿物转化的机制提供相当大的见解。赤铁矿与Fe(II)-草酸盐之间的自催化相互作用因其环境和工业意义而长期受到关注。在这项研究中,我们利用铁同位素标记和单颗粒尺度的质量敏感成像来确定溶液成分的变化如何与多面、微米大小的赤铁矿血小板的形态演化相关。净溶解是通过分析水铁化学,以及定量原子力显微镜证实。同位素作图技术表明,在不存在草酸盐的情况下,Fe(II)很容易吸附在(001)和(012)表面,但当草酸盐存在时,(001)表面发生选择性溶解,并且没有观察到57Fe通过再结晶沉积。与铁(II)、草酸盐和铁(II)-草酸盐反应后的颗粒微观形貌比较显示出本质上不同的行为,与赤铁矿表面不同的相互作用机制相一致。在该体系中对溶液/固体耦合动力学进行了广泛的表征,为区分晶体生长、溶解和再结晶过程提供了新的见解。
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来源期刊
Environmental Science: Nano
Environmental Science: Nano CHEMISTRY, MULTIDISCIPLINARY-ENVIRONMENTAL SCIENCES
CiteScore
12.20
自引率
5.50%
发文量
290
审稿时长
2.1 months
期刊介绍: Environmental Science: Nano serves as a comprehensive and high-impact peer-reviewed source of information on the design and demonstration of engineered nanomaterials for environment-based applications. It also covers the interactions between engineered, natural, and incidental nanomaterials with biological and environmental systems. This scope includes, but is not limited to, the following topic areas: Novel nanomaterial-based applications for water, air, soil, food, and energy sustainability Nanomaterial interactions with biological systems and nanotoxicology Environmental fate, reactivity, and transformations of nanoscale materials Nanoscale processes in the environment Sustainable nanotechnology including rational nanomaterial design, life cycle assessment, risk/benefit analysis
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