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过氧化氢作为饱和含水层系统中生物修复活动氧源的命运

The Fate of Hydrogen Peroxide as an Oxygen Source for Bioremediation Activities within Saturated Aquifer Systems.

作者信息

Zappi Mark, White Kenneth, Hwang Huey-Min, Bajpai Rakesh, Qasim Mohammad

机构信息

a Department of Chemical Engineering , Mississippi State University.

b Georgia Department of Natural Resources.

出版信息

J Air Waste Manag Assoc. 2000 Oct;50(10):1818-1830. doi: 10.1080/10473289.2000.10464207.

Abstract

In situ bioremediation is an innovative technique for the remediation of contaminated aquifers that involves the use of microorganisms to remediate soils and groundwaters polluted by hazardous substances. During its application, this process may require the addition of nutrients and/or electron acceptors to stimulate appropriate biological activity. Hydrogen peroxide has been commonly used as an oxygen source because of the limited concentrations of oxygen that can be transferred into the groundwater using above-ground aeration followed by reinjection of the oxygenated groundwater into the aquifer or subsurface air sparging of the aquifer. Because of several potential interactions of HO with various aquifer material constituents, its decomposition may be too rapid, making effective introduction of the HO into targeted treatment zones extremely difficult and costly. Therefore, a bench-scale study was conducted to determine the fate of HO within subsurface aquifer environments. The purpose of this investigation was to identify those aquifer constituents, both biotic and abiotic, that are most active in controlling the fate of HO. The decomposition rates of HO were determined using both equilibrated water samples and soil slurries. Results showed HO decomposition to be effected by several commonly found inorganic soil components; however, biologically mediated catalytic reactions were determined to be the most substantial.

摘要

原位生物修复是一种用于修复受污染含水层的创新技术,该技术利用微生物来修复被有害物质污染的土壤和地下水。在其应用过程中,此过程可能需要添加营养物质和/或电子受体以刺激适当的生物活性。由于通过地面曝气将氧气转移到地下水中,然后将含氧地下水重新注入含水层或对含水层进行地下空气喷射,能够转移到地下水中的氧气浓度有限,因此过氧化氢一直被用作氧气源。由于过氧化氢(HO)与各种含水层物质成分存在多种潜在相互作用,其分解可能过于迅速,使得将过氧化氢有效引入目标处理区域极其困难且成本高昂。因此,开展了一项实验室规模的研究,以确定过氧化氢在地下含水层环境中的归宿。本研究的目的是确定那些在控制过氧化氢归宿方面最具活性的含水层成分,包括生物成分和非生物成分。使用平衡水样和土壤泥浆来测定过氧化氢的分解速率。结果表明,过氧化氢的分解受到几种常见无机土壤成分的影响;然而,生物介导的催化反应被确定为最主要的因素。

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