Geology topics

C. J. Ballentine

Publications and source records attributed to C. J. Ballentine.

3 recordsLinked to original sources

USGS2021

Noble gas signatures constrain oil-field water as the carrier phase of hydrocarbons occurring in shallow aquifers in the San Joaquin Basin, USA

Noble gases record fluid interactions in multiphase subsurface environments through fractionation processes during fluid equilibration. Water in the presence of hydrocarbons at the subsurface acquires a distinct elemental signature due to the difference in solubility between these two fluids. We find the atmospheric noble gas signature in produced water is partially preserved after hydrocarbons production and water disposal to unlined ponds at the surface. This signature is distinct from meteoric water and can be used to trace oil-field water seepage into groundwater aquifers. We analyse groundwater ( n = 30) and fluid disposal pond ( n = 2) samples from areas overlying or adjacent to the Fruitvale, Lost Hills, and South Belridge Oil Fields in the San Joaquin Basin, California, USA. Methane (2.8 × 10 −7 to 3 × 10 −2 cm 3 STP/cm 3 ) was detected in 27 of 30 groundwater samples. Using atmospheric noble gas signatures, the presence of oil-field water was identified in 3 samples, which had equilibrated with thermogenic hydrocarbons in the reservoir. Two (of the three) samples also had a shallow microbial methane component, acquired when produced water was deposited in a disposal pond at the surface. An additional 6 samples contained benzene and toluene, indicative of interaction with oil-field water; however, the noble gas signatures of these samples are not anomalous. Based on low tritium and 14 C contents (≤ 0.3 TU and 0.87–6.9 pcm, respectively), the source of oil-field water is likely deep, which could include both anthropogenic and natural processes. Incorporating noble gas analytical techniques into the groundwater monitoring programme allows us to 1) differentiate between thermogenic and microbial hydrocarbon gas sources in instances when methane isotope data are unavailable, 2) identify the carrier phase of oil-field constituents in the aquifer (gas, oil-field water, or a combination), and 3) differentiate between leakage from a surface source (disposal ponds) and from the hydrocarbon reservoir (either along natural or anthropogenic pathways such as faulty wells).

California↗

USGS2021

Investigating the effect of enhanced oil recovery on the noble gas signature of casing gases and produced waters from selected California oil fields

In regions where water resources are scarce and in high demand, it is important to safeguard against contamination of groundwater aquifers by oil-field fluids (water, gas, oil). In this context, the geochemical characterisation of these fluids is critical so that anthropogenic contaminants can be readily identified. The first step is characterising pre-development geochemical fluid signatures (i.e., those unmodified by hydrocarbon resource development) and understanding how these signatures may have been perturbed by resource production, particularly in the context of enhanced oil recovery (EOR) techniques. Here, we present noble gas isotope data in fluids produced from oil wells in several water-stressed regions in California, USA, where EOR is prevalent. In oil-field systems, only casing gases are typically collected and measured for their noble gas compositions, even when oil and/or water phases are present, due to the relative ease of gas analyses. However, this approach relies on a number of assumptions (e.g., equilibrium between phases, water-to-oil ratio (WOR) and gas-to-oil ratio (GOR) in order to reconstruct the multiphase subsurface compositions. Here, we adopt a novel, more rigorous approach, and measure noble gases in both casing gas and produced fluid (oil-water-gas mixtures) samples from the Lost Hills, Fruitvale, North and South Belridge (San Joaquin Basin, SJB) and Orcutt (Santa Maria Basin) Oil Fields. Using this method, we are able to fully characterise the distribution of noble gases within a multiphase hydrocarbon system. We find that measured concentrations in the casing gases agree with those in the gas phase in the produced fluids and thus the two sample types can be used essentially interchangeably. EOR signatures can readily be identified by their distinct air-derived noble gas elemental ratios (e.g., 20 Ne/ 36 Ar), which are elevated compared to pre-development oil-field fluids, and conspicuously trend towards air values with respect to elemental ratios and overall concentrations. We reconstruct reservoir 20 Ne/ 36 Ar values using both casing gas and produced fluids and show that noble gas ratios in the reservoir are strongly correlated (r 2 = 0.88–0.98) to the amount of water injected within ~500 m of a well. We suggest that the 20 Ne/ 36 Ar increase resulting from injection is sensitive to the volume of fluid interacting with the injectate, the effective water-to-oil ratio, and the composition of the injectate. Defining both the pre-development and injection-modified hydrocarbon reservoir compositions are crucial for distinguishing the sources of hydrocarbons observed in proximal groundwaters, and for quantifying the transport mechanisms controlling this occurrence.

California↗

USGS2019

A novel method for the extraction, purification and characterization of noble gases in produced fluids

Hydrocarbon systems with declining or viscous oil production are often stimulated using enhanced oil recovery (EOR) techniques, such as the injection of water, steam and CO2, in order to increase oil and gas production. As EOR and other methods of enhancing production such as hydraulic fracturing have become more prevalent, environmental concerns about the impact of both new and historical hydrocarbon production on overlying shallow aquifers have increased. Noble gas isotopes are powerful tracers of subsurface fluid provenance and can be used to understand the impact of EOR on hydrocarbon systems and potentially overlying aquifers. In oil systems, produced fluids can consist of a mixture of oil, water and gas. Noble gases are typically measured in the gas phase; however, it is not always possible to collect gases and therefore produced fluids (which are water, oil and gas mixtures) must be analyzed. We outline a new technique to separate and analyze noble gases in multi-phase hydrocarbon-associated fluid samples. An offline double capillary method has been developed to quantitatively isolate noble gases into a transfer vessel, while effectively removing all water, oil, and less volatile hydrocarbons. The gases are then cleaned and analyzed using standard techniques. Air-saturated water reference materials (n=24) were analyzed and results show a method reproducibility of 2.9% for 4He, 3.8% for 20Ne, 4.5% for 36Ar, 5.3% for 84Kr and 5.7% for 132Xe. This new technique was used to measure the noble gas isotopic compositions in six produced fluid samples from the Fruitvale Oil Field, Bakersfield, California.

Geochemistry, Geophysics, Geosystems↗