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Redox microniches in groundwater: A model study on the geometric and kinetic conditions required for concomitant Fe oxide reduction, sulfate reduction, and methanogenesis

机译:地下水中的氧化还原微生态位:有关氧化铁还原,硫酸盐还原和甲烷生成所需的几何和动力学条件的模型研究

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摘要

A pore-scale model using PHAST is used to study the distribution of redox processes and other geochemical processes in intergranular and intragranular microniches in a groundwater system. The goal is to determine the geometric and kinetic conditions that may give rise to the presence of methane under Fe oxide and sulfate reducing conditions. The model includes FeS precipitation, calcite dissolution and precipitation, and an extended partial equilibrium description of the redox processes: Fe oxide reduction, sulfate reduction, and methanogenesis/methane oxidation, which takes the microbial energy requirements into account. The model indicates that a separation of redox processes within the pore space is possible, if the stagnant pores are deep and narrow and the rate of organic matter decomposition is fast. However, in most aquifers the organic matter reactivity will be so low that isolated lumps or actual layers of organic matter rather than particles or intragranular coatings of organic matter are required in order to produce methanogenic conditions; otherwise sulfate reduction will take place in the stagnant parts. In the model, the redox processes lead to localized secondary processes occurring at the grain scale; for example, the oxidation of organic matter in a microniche releases CO_2 which dissolves calcite, which is reprecipitated where the Fe oxides are being dissolved and reduced because of the locally increased pH.
机译:使用PHAST的孔隙尺度模型用于研究地下水系统中颗粒间和颗粒内微生态位中氧化还原过程和其他地球化学过程的分布。目的是确定在Fe氧化物和硫酸盐还原条件下可能引起甲烷存在的几何和动力学条件。该模型包括FeS沉淀,方解石溶解和沉淀,以及氧化还原过程的扩展部分平衡描述:Fe氧化物的还原,硫酸盐的还原和甲烷生成/甲烷的氧化,其中考虑了微生物的能量需求。该模型表明,如果停滞的孔隙深而狭窄且有机物分解速度快,则可以在孔隙空间中分离氧化还原过程。但是,在大多数含水层中,有机物的反应性很低,以至于不能产生有机物的团块或实际层,而是为了产生产甲烷条件而需要有机物的颗粒或颗粒内涂层。否则,停滞部位将发生硫酸盐还原。在模型中,氧化还原过程导致在晶粒尺度上发生局部二次过程。例如,小生境中有机物的氧化会释放出溶解方解石的CO_2,由于pH的局部升高,在溶解和还原Fe氧化物的地方重新沉淀。

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