SusChEM: Collaborative Research: Influence of Fe2+- catalyzed recrystallization on Fe oxide reactivity and C stabilization

SusChEM：合作研究：Fe2 催化重结晶对 Fe 氧化物反应性和 C 稳定性的影响

• 批准号: 1451494
• 负责人: Thomas Borch
• 金额: $ 8.7万
• 依托单位: Colorado State University
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-08-01 至 2018-07-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=1451494&HistoricalAwards=false
• 关键词: SusChEM; Collaborative; Research; Influence; Fe2+

Iron (Fe) is the fourth most abundant element on Earth and a critical nutrient for all life (from microorganisms to humans). Iron minerals are an important part of our lives: they are part of the soil beneath our feet; the rust on our cars; the hard drives in our computers; and the rocks on Earth and Mars. These tiny, often nanoscale, particles are responsible for most of the red, yellow, green, and black colors around us and they profoundly influence the quality of our water, air, and soil through biologically-driven redox cycling between oxidized ferric iron (Fe3+) and reduced ferrous iron (Fe2+). These Fe minerals trap much of the organic carbon (C) in soils and sediments and can also take the place of oxygen in anaerobic respiration, oxidizing and mineralizing organic matter to CO2 in anoxic soils and sediments. Increasing concerns about carbon driven climate change provides strong motivation to better understand the coupling between Fe and C processes that govern storage of carbon (C) in soils and sediments. The research findings from this work will benefit society by providing important insights into terrestrial response to climate change, as well as water quality preservation (such as arsenic release), and engineered water treatment systems. This project will provide authentic research experiences for individuals from groups underrepresented in the sciences at the upper high school (HS) and undergraduate (UG) levels. This will be accom-plished by involving long-term UG researchers in the project; providing HS junior and seniors from schools with historically low-college enrollment opportunities to participate in authentic summer research activities; and providing direct faculty-student instruction for HS and UG students as part of a ?Scale-Matters? workshop and Summer Soil Institute. The overall goal of this research project is to understand the complex redox dynamics between Fe and organic C soils and sediments. In reducing environments, dissolved Fe2+ can catalyze Fe oxides to recrystallize into new mineral phases with similar or drastically different chemical properties. This process, Fe2+- catalyzed recrystallization, has been observed for pure Fe phases, but has yet to be explored as a pathway for mobilizing (or sequestering) organic C. Additionally, the presence of organic C is also likely to alter the recrystallization process with important implications for the Fe reactivity and isotope fractionation. The investigators will investigate how Fe2+- catalyzed recrystallization influences organic C and Fe mineral reactivity. To do this, the investigators will conduct a series of Fe isotope tracer experiments to quantify the extent of Fe2+- catalyzed recrystallization in model Fe-C assemblages synthesized from a range of Fe oxides and diversity of natural organic matter. Changes in Fe oxide susceptibility to microbial and chemical dissolution will be measured, along with Fe isotopic fractionation, and C availability following recrystallization of the Fe-C assemblages.

铁（Fe）是地球上含量第四丰富的元素，也是所有生命（从微生物到人类）的重要营养物质。铁矿是我们生活的重要组成部分：它们是我们脚下土壤的一部分；我们汽车上的锈；我们电脑里的硬盘；地球和火星上的岩石。这些微小的，通常是纳米级的颗粒是我们周围大部分红色、黄色、绿色和黑色的原因，它们通过在氧化三铁（Fe3+）和还原亚铁（Fe2+）之间的生物驱动的氧化还原循环，深刻地影响着我们的水、空气和土壤的质量。这些铁矿物捕获了土壤和沉积物中的大部分有机碳(C)，也可以在厌氧呼吸中代替氧气，将缺氧土壤和沉积物中的有机物氧化并矿化为二氧化碳。对碳驱动的气候变化的日益关注为更好地理解铁和碳过程之间的耦合提供了强大的动力，这些耦合控制着土壤和沉积物中碳(C)的储存。这项工作的研究结果将通过提供关于陆地对气候变化的反应、水质保存（如砷释放）和工程水处理系统的重要见解而造福社会。该项目将为来自高中（HS）和本科（UG）水平的科学中代表性不足的群体的个人提供真实的研究经验。这将通过让长期的UG研究人员参与项目来实现；为来自历史上低入学率学校的高三学生提供参加真正的暑期研究活动的机会；并为高中和大学学生提供直接的师生指导，作为“Scale-Matters”项目的一部分。研讨会和夏季土壤研究所。本研究项目的总体目标是了解铁与有机碳土壤和沉积物之间复杂的氧化还原动力学。在还原环境中，溶解的Fe2+可以催化Fe氧化物重结晶成化学性质相似或截然不同的新矿物相。这一过程，即Fe2+催化的再结晶，已经在纯铁相中被观察到，但尚未被探索作为调动（或隔离）有机C的途径。此外，有机C的存在也可能改变再结晶过程，对铁的反应性和同位素分馏具有重要意义。研究人员将研究Fe2+催化的再结晶如何影响有机C和Fe矿物的反应性。为此，研究人员将进行一系列铁同位素示踪实验，以量化由一系列铁氧化物和多种天然有机物合成的模型Fe- c组合中Fe2+催化的再结晶程度。将测量铁氧化物对微生物和化学溶解敏感性的变化，以及铁同位素分馏和铁-碳组合再结晶后的C可用性。