Department of Civil and Environmental Engineering, Colorado State University, Fort Collins, CO 80523, United States; Department of Civil and Environmental Engineering, University of New Hampshire, Durham, NH 03824, United States.
Department of Civil and Environmental Engineering, University of New Hampshire, Durham, NH 03824, United States.
Sci Total Environ. 2019 Jun 10;668:1094-1103. doi: 10.1016/j.scitotenv.2019.03.041. Epub 2019 Mar 13.
Hydraulic fracturing fluids are injected into unconventional oil and gas systems to stimulate hydrocarbon production, returning to the surface in flowback and produced waters containing a complex mixture of xenobiotic additives and geogenic compounds. Nonionic polyethoxylates are commonly added surfactants that act as weatherizers, emulsifiers, wetting agents, and corrosion inhibitors in hydraulic fracturing fluid formulations. Understanding the biodegradability of these ubiquitous additives is critical for produced water pre-treatment prior to reuse and for improving treatment trains for external beneficial reuse. The objective of this study was to determine the effect of produced water total dissolved solids (TDS) from an unconventional natural gas well on the aerobic biodegradation of alkyl ethoxylate and nonylphenol ethoxylate surfactants. Changes in surfactant concentrations, speciation and metabolites, as well as microbial community composition and activity were quantified over a 75-day aerobic incubation period. Alkyl ethoxylates (AEOs) were degraded faster than nonylphenol ethoxylates (NPEOs), and both compound classes and bulk organic carbon biodegraded slower in TDS treatments (10 g L, 40 g L) as compared to controls. Short-chain ethoxylates were more rapidly biodegraded than longer-chain ethoxylates, and changes in the relative abundance of metabolites including acetone, alcohols, and carboxylate and aldehyde intermediates of alkyl units indicated metabolic pathways may shift in the presence of higher produced water TDS. Our key finding that polyethoxylated alcohol surfactant additives are less labile at high TDS has important implications for produced water management, as these fluids are increasingly recycled for beneficial reuse in hydraulic fracturing fluids and other purposes.
水力压裂液被注入非常规的石油和天然气系统中,以刺激碳氢化合物的生产,在返排和产出水中回到地面,这些水含有复杂的异生物质添加剂和地质化合物的混合物。非离子型聚氧乙烯醚通常是作为调湿剂、乳化剂、润湿剂和腐蚀抑制剂添加到水力压裂液配方中的表面活性剂。了解这些普遍存在的添加剂的可生物降解性对于产出水在再利用之前的预处理以及改进外部有益再利用的处理途径至关重要。本研究的目的是确定来自非常规天然气井的产出水总溶解固体(TDS)对烷基乙氧基化物和壬基酚乙氧基化物表面活性剂好氧生物降解的影响。在 75 天的好氧培养期间,定量了表面活性剂浓度、形态和代谢物的变化,以及微生物群落组成和活性的变化。与对照相比,烷基乙氧基化物(AEOs)的降解速度快于壬基酚乙氧基化物(NPEOs),并且在 TDS 处理(10g/L、40g/L)中,两种化合物类别和总有机碳的生物降解速度都较慢。短链乙氧基化物比长链乙氧基化物更快地被生物降解,并且代谢物的相对丰度的变化,包括丙酮、醇和羧酸以及烷基单元的醛中间体表明在存在较高的产出水 TDS 时,代谢途径可能会发生变化。我们的主要发现是,在高 TDS 条件下,聚氧乙烯醇表面活性剂添加剂的稳定性较差,这对产出水管理具有重要意义,因为这些流体越来越多地被回收用于水力压裂液和其他用途的有益再利用。