Layer-to-tunnel manganese oxides transformation triggered by pyrogenic carbon and trace metals: Key role of reducing and oxidizing components cooperation

IF 4.5 1区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Zibo Xu , Bin Ma , Yuanzhi Tang , Daniel C.W. Tsang
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Abstract

Manganese oxide (MnOx) plays crucial roles in shaping various environmental and geochemistry processes, with their reactivity largely dependent on the structure of MnOx. Tunnel MnOx effectively hosts a substantial quantity of soil elements within its tunnel structure, exerting significant control over element turnover and pertinent geochemical processes, while the precise determinants regarding the layer-to-tunnel transformation of MnOx with electron transfer remain unclear. In this study, we delved into the transformation of layer-structured MnOx during the interaction with coexisting soil redox components (pyrogenic carbon and Tl with differing redox reactivity). Our findings revealed that the transformation from layer to tunnel structure only occurred in the presence of reductive pyrogenic carbon and oxidative Tl(III) rather than sole reductants/oxidants within a short incubation period of 6 weeks. The macro reducing environment created by the pyrogenic carbon and the micro oxidizing environment related to the Tl(III) chelation was pivotal in the cyclic valence change of Mn, resulting in the generation of Mn(III) and vacancies in the Mn structure, the prerequisite for the layer-to-tunnel transformation. Anchoring of oxidative Tl(III) on the surface or inside the tunnel structure of MnOx through Tl–O–Mn bonding was the key to building a micro oxidative environment under bulk-reducing conditions. During the transformation, Tl was integrated into the tunnel of high-crystallinity MnOx, and prolonged incubation resulted in the deeper embedding of Tl and the formation of atomic clusters. The embedding of Tl inside of the tunnel MnOx led to lower solubility and bioaccessibility, with only 0.05–0.26 mg Kg−1 being extracted with soil organic acids through reductive dissolution and 8.7–8.9 % by in vitro physiologically based extraction test. This study underscores the significant role of electron-donating and electron-accepting components in triggering interconnected geochemical processes with MnOx, carbon, and trace elements.
热源碳和痕量金属引发的层间锰氧化物转化:还原和氧化成分合作的关键作用
氧化锰(MnOx)在形成各种环境和地球化学过程中起着至关重要的作用,其反应性在很大程度上取决于氧化锰的结构。隧道氧化锰在其隧道结构中有效地容纳了大量的土壤元素,对元素转换和相关地球化学过程具有重要的控制作用,但氧化锰通过电子转移实现从层到隧道转化的确切决定因素仍不清楚。在本研究中,我们深入研究了层状结构氧化锰在与共存的土壤氧化还原成分(具有不同氧化还原反应性的火成碳和碲)相互作用过程中的转变。我们的研究结果表明,在 6 周的短培养期内,只有在还原性火成碳和氧化性 Tl(III)的存在下,而不是仅在还原剂/氧化剂的存在下,才会发生从层结构到隧道结构的转变。热原碳创造的宏观还原环境和与 Tl(III)螯合相关的微观氧化环境在锰的循环价态变化中起着关键作用,导致锰(III)的生成和锰结构中的空位,这是层到隧道转变的先决条件。通过 Tl-O-Mn 键将氧化性 Tl(III)锚定在 MnOx 表面或隧道结构内部,是在大量还原条件下建立微氧化环境的关键。在转化过程中,Tl 被整合到高结晶度 MnOx 的隧道中,长时间的培养导致 Tl 深度嵌入并形成原子团簇。隧道氧化锰内部的钛包埋导致溶解度和生物可及性降低,通过还原溶解,土壤有机酸只能提取 0.05-0.26 mg Kg-1 的钛,体外生理学萃取试验只能提取 8.7-8.9 % 的钛。这项研究强调了电子供体和电子受体成分在引发氧化锰、碳和微量元素相互关联的地球化学过程中的重要作用。
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来源期刊
Geochimica et Cosmochimica Acta
Geochimica et Cosmochimica Acta 地学-地球化学与地球物理
CiteScore
9.60
自引率
14.00%
发文量
437
审稿时长
6 months
期刊介绍: Geochimica et Cosmochimica Acta publishes research papers in a wide range of subjects in terrestrial geochemistry, meteoritics, and planetary geochemistry. The scope of the journal includes: 1). Physical chemistry of gases, aqueous solutions, glasses, and crystalline solids 2). Igneous and metamorphic petrology 3). Chemical processes in the atmosphere, hydrosphere, biosphere, and lithosphere of the Earth 4). Organic geochemistry 5). Isotope geochemistry 6). Meteoritics and meteorite impacts 7). Lunar science; and 8). Planetary geochemistry.
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