The synergistic effect of calcium on organic carbon sequestration to ferrihydrite

IF 0.9 4区 地球科学 Q4 GEOCHEMISTRY & GEOPHYSICS
Tyler D. Sowers, Jason W. Stuckey, Donald L. Sparks
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引用次数: 65

Abstract

Sequestration of organic carbon (OC) in environmental systems is critical to mitigating climate change. Organo-mineral associations, especially those with iron (Fe) oxides, drive the chemistry of OC sequestration and stability in soils. Short-range-ordered Fe oxides, such as ferrihydrite, demonstrate a high affinity for OC in binary systems. Calcium commonly co-associates with OC and Fe oxides in soils, though the bonding mechanism (e.g., cation bridging) and implications of the co-association for OC sequestration remain unresolved. We explored the effect of calcium (Ca2+) on the sorption of dissolved OC to 2-line ferrihydrite. Sorption experiments were conducted between leaf litter-extractable OC and ferrihydrite at pH 4 to 9 with different initial C/Fe molar ratios and Ca2+ concentrations. The extent of OC sorption to ferrihydrite in the presence of Ca2+ increased across all tested pH values, especially at pH ≥?7. Sorbed OC concentration at pH 9 increased from 8.72?±?0.16 to 13.3?±?0.20?mmol OC g?1 ferrihydrite between treatments of no added Ca2+ and 30?mM Ca2+ addition. Batch experiments were paired with spectroscopic studies to probe the speciation of sorbed OC and elucidate the sorption mechanism. ATR-FTIR spectroscopy analysis revealed that carboxylic functional moieties were the primary sorbed OC species that were preferentially bound to ferrihydrite and suggested an increase in Fe-carboxylate ligand exchange in the presence of Ca at pH 9. Results from batch to spectroscopic experiments provide significant evidence for the enhancement of dissolved OC sequestration to 2-line ferrihydrite and suggest the formation of Fe–Ca-OC ternary complexes. Findings of this research will inform modeling of environmental C cycling and have the potential to influence strategies for managing land to minimize OM stabilization.

Abstract Image

钙对水合铁有机碳固存的协同效应
环境系统中有机碳的固存对减缓气候变化至关重要。有机矿物结合,特别是那些含铁(Fe)氧化物的结合,推动土壤中有机碳的化学封存和稳定性。短程有序铁氧化物,如水合铁,在二元体系中表现出对氧化碳的高亲和力。在土壤中,钙通常与有机碳和铁氧化物共结合,尽管其结合机制(如阳离子桥接)和共结合对有机碳封存的影响尚不清楚。我们探讨了钙(Ca2+)对二线水合铁吸附溶解OC的影响。在pH为4 ~ 9、初始C/Fe摩尔比和Ca2+浓度不同的条件下,进行了叶片凋落物可萃取OC与水合铁的吸附实验。在Ca2+存在的情况下,OC对水合铁的吸附程度在所有pH值下都有所增加,特别是在pH≥?7时。pH = 9时吸附的OC浓度从8.72±0.16增加到13.3±0.20。mmol OC g?不添加Ca2+处理与30?mM Ca2+的加入。采用批量实验与光谱研究相结合的方法,探讨了吸附OC的形态,阐明了吸附机理。ATR-FTIR光谱分析表明,羧酸官能团是主要吸附的OC物种,优先与铁水合物结合,表明在pH为9时Ca存在下,fe -羧酸盐配体交换增加。从批量实验到光谱实验的结果都提供了明显的证据,证明溶解的OC对二线水合铁的吸附增强,并表明形成了Fe-Ca-OC三元配合物。这项研究的结果将为环境碳循环的建模提供信息,并有可能影响管理土地的策略,以最大限度地减少有机质的稳定。
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来源期刊
Geochemical Transactions
Geochemical Transactions 地学-地球化学与地球物理
CiteScore
3.70
自引率
4.30%
发文量
2
审稿时长
>12 weeks
期刊介绍: Geochemical Transactions publishes high-quality research in all areas of chemistry as it relates to materials and processes occurring in terrestrial and extraterrestrial systems.
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