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在控制天然气释放实验过程中,地下水溶解气体的高分辨率时空演化。

High resolution spatial and temporal evolution of dissolved gases in groundwater during a controlled natural gas release experiment.

机构信息

G360 Institute for Groundwater Research, College of Engineering & Physical Sciences, University of Guelph, Ontario, Canada; Energy and Environment Research Initiative, Department of Earth, Ocean and Atmospheric Science, University of British Columbia, BC, Canada.

G360 Institute for Groundwater Research, College of Engineering & Physical Sciences, University of Guelph, Ontario, Canada.

出版信息

Sci Total Environ. 2018 May 1;622-623:1178-1192. doi: 10.1016/j.scitotenv.2017.12.049. Epub 2017 Dec 13.

Abstract

Fugitive gas comprised primarily of methane (CH) with traces of ethane and propane (collectively termed C) may negatively impact shallow groundwater when unintentionally released from oil and natural gas wells. Currently, knowledge of fugitive gas migration, subsurface source identification and oxidation potential in groundwater is limited. To advance understanding, a controlled release experiment was performed at the Borden Research Aquifer, Canada, whereby 51m of natural gas was injected into an unconfined sand aquifer over 72days with dissolved gases monitored over 323days. During active gas injection, a dispersed plume of dissolved C evolved in a depth discrete and spatially complex manner. Evolution of the dissolved gas plume was driven by free-phase gas migration controlled by small-scale sediment layering and anisotropy. Upon cessation of gas injection, C concentrations increased to the greatest levels observed, particularly at 2 and 6m depths, reaching up to 31.5, 1.5 and 0.1mg/L respectively before stabilizing and persisting. At no time did groundwater become fully saturated with natural gas at the scale of sampling undertaken. Throughout the experiment the isotopic composition of injected methane (δC of -42.2‰) and the wetness parameter (i.e. the ratio of C to C) constituted excellent tracers for the presence of fugitive gas at concentrations >2mg/L. At discrete times C concentrations varied by up to 4 orders of magnitude over 8m of aquifer thickness (e.g. from <0.01 to 30mg/L for CH), while some groundwater samples lacked evidence of fugitive gas, despite being within 10m of the injection zone. Meanwhile, carbon isotope ratios of dissolved CH showed no evidence of oxidation. Our results show that while impacts to aquifers from a fugitive gas event are readily detectable at discrete depths, they are spatially and temporally variable and dissolved methane has propensity to persist.

摘要

主要由甲烷(CH)和少量乙烷和丙烷(统称为 C)组成的逸散气在无意中从油井和天然气井中释放出来时可能会对浅层地下水产生负面影响。目前,对逸散气迁移、地下源识别和地下水氧化潜力的了解有限。为了深入了解这一问题,在加拿大伯登研究含水层进行了一项受控释放实验,在 72 天内将 51m3 的天然气注入无压砂含水层,在 323 天内监测溶解气体。在天然气的活跃注入期间,溶解 C 的离散和空间复杂的弥散羽流不断演变。溶解气体羽流的演化是由小尺度沉积物层理和各向异性控制的自由相气体迁移驱动的。在停止注入天然气后,C 浓度增加到观察到的最大水平,特别是在 2 和 6m 深度处,分别达到 31.5、1.5 和 0.1mg/L,然后稳定并持续存在。在采样的规模上,地下水从未完全饱和过天然气。在整个实验过程中,注入甲烷的同位素组成(δC 为-42.2‰)和湿度参数(即 C 与 C 的比值)是存在逸散气(浓度>2mg/L)的极好示踪剂。在离散时间内,C 浓度在 8m 含水层厚度内变化了 4 个数量级(例如,CH 的浓度从<0.01 到 30mg/L),而一些地下水样本尽管距离注入区不到 10m,但没有逸散气的证据。同时,溶解 CH 的碳同位素比值没有氧化的证据。我们的结果表明,尽管在离散深度很容易检测到逸散气事件对含水层的影响,但它们在空间和时间上是可变的,并且溶解甲烷有持续存在的倾向。

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