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两性氧化胺基表面活性剂的好氧生物降解:分子结构、初始表面活性剂浓度和pH值的影响

Aerobic biodegradation of amphoteric amine-oxide-based surfactants: Effect of molecular structure, initial surfactant concentration and pH.

作者信息

Ríos Francisco, Lechuga Manuela, Fernández-Serrano Mercedes, Fernández-Arteaga Alejandro

机构信息

Department of Chemical Engineering, Faculty of Science, University of Granada, Campus Fuentenueva s/n, 18071, Granada, Spain.

Department of Chemical Engineering, Faculty of Science, University of Granada, Campus Fuentenueva s/n, 18071, Granada, Spain.

出版信息

Chemosphere. 2017 Mar;171:324-331. doi: 10.1016/j.chemosphere.2016.12.070. Epub 2016 Dec 18.

Abstract

The present study was designed to provide information regarding the effect of the molecular structure of amphoteric amine-oxide-based surfactants and the initial surfactant concentration on their ultimate biodegradation. Moreover, given this parameter's pH-dependence, the effect of pH was also investigated. Three amine-oxide-based surfactants with structural differences in their hydrophobic alkyl chain were tested: Lauramine oxide (AO-R), Myristamine oxide (AO-R) and Cocamidopropylamine oxide (AO-Cocoamido). We studied the ultimate biodegradation using the Modified OECD Screening Test at initial surfactant concentrations ranged from 5 to 75 mg L and at pH levels from 5 to 7.4. The results demonstrate that at pH 7.4, amine-oxide-based surfactants are readily biodegradable. In this study, we concluded that ω-oxidation can be assumed to be the main biodegradation pathway of amine-oxides and that differences in the biodegradability between them can be explained by the presence of an amide group in the alkyl chain of AO-Cocoamido; the CN fission of the amide group slows down their mineralization process. In addition, the increase in the concentration of the surfactant from 5 to 75 mg L resulted in an increase in the final biodegradation of AO-R and AO-R. However, in the case of AO-Cocoamido, a clear relationship between the concentration and biodegradation cannot be stated. Conversely, the biodegradability of AO-R and AO-R was considerably lower in an acid condition than at a pH of 7.4, whereas AO-Cocoamido reached similar percentages in acid conditions and at a neutral pH. However, microorganisms required more time to acclimate.

摘要

本研究旨在提供有关两性氧化胺基表面活性剂的分子结构和初始表面活性剂浓度对其最终生物降解作用的信息。此外,鉴于该参数对pH的依赖性,还研究了pH的影响。测试了三种疏水烷基链结构不同的氧化胺基表面活性剂:月桂基氧化胺(AO-R)、肉豆蔻基氧化胺(AO-R)和椰油酰胺丙基氧化胺(AO-Cocoamido)。我们使用改进的经合组织筛选试验,在初始表面活性剂浓度为5至75mg/L以及pH值为5至7.4的条件下研究了最终生物降解情况。结果表明,在pH 7.4时,氧化胺基表面活性剂易于生物降解。在本研究中,我们得出结论,ω-氧化可被认为是氧化胺的主要生物降解途径,并且它们之间生物降解性的差异可以通过AO-Cocoamido烷基链中存在酰胺基团来解释;酰胺基团的碳氮键断裂减缓了它们的矿化过程。此外,表面活性剂浓度从5mg/L增加到75mg/L导致AO-R和AO-R的最终生物降解增加。然而,对于AO-Cocoamido,无法说明浓度与生物降解之间存在明确关系。相反,在酸性条件下,AO-R和AO-R的生物降解性比在pH 7.4时低得多,而AO-Cocoamido在酸性条件和中性pH下达到相似的百分比。然而,微生物需要更多时间来适应。

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