Devon Renock | Geology Reports

USGS2019

Effects of organic ligands and background electrolytes on barite dissolution

Barite dissolution rates and features were investigated under conditions that combine a variety of organic ligands with different background electrolyte solutions. The organic ligands included low molecular weight organic compounds (LMWO) that can be produced by halophilic bacteria and are common in natural environments, as well as synthetic chelators that were previously studied in barite dissolution. Background electrolyte solutions included deionized water, 0.72 M NaCl and 2 M NaCl solutions designed to simulate freshwater, seawater, and brine fluids, respectively. Barite dissolution rates and corresponding rate constants normalized for saturation states were calculated for most experiments. Equal or lower rates and rate constants for pure LMWO relative to controls at all background electrolyte concentrations and pH values indicated that LMWO do not promote barite dissolution. Synthetic chelators showed higher rates and rate constants at pH 10 at static conditions than controls, indicating enhanced barite dissolution. Distinctive etch pit morphologies on the barite (0 0 1) face were observed in the presence of synthetic chelators, suggesting a direct contact dissolution mechanism by synthetic chelators. The effect of synthetic chelators on barite dissolution was significantly reduced in the presence of 2 M NaCl and/or at pH 6.5 due to salting out effects. Under hypersaline conditions, barite dissolution rates and rate constants by bacterial activities were up to four times higher than those of synthetic chelators. The wide range of conditions studied in this work provides insights into prediction of barite dissolution behavior in various natural environments as well as in industrial treatment procedures.

Geochimica et Cosmochimica Acta↗

USGS2017

Microbially mediated barite dissolution in anoxic brines

Fluids injected into shale formations during hydraulic fracturing of black shale return with extraordinarily high total-dissolved-solids (TDS) and high concentrations of barium (Ba) and radium (Ra). Barite, BaSO 4 , has been implicated as a possible source of Ba as well as a problematic mineral scale that forms on internal well surfaces, often in close association with radiobarite, (Ba,Ra)SO 4 . The dissolution of barite by abiotic processes is well quantified. However, the identification of microbial communities in flowback and produced water necessitates the need to understand barite dissolution in the presence of bacteria. Therefore, we evaluated the rates and mechanisms of abiotic and microbially-mediated barite dissolution under anoxic and hypersaline conditions in the laboratory. Barite dissolution experiments were conducted with bacterial enrichment cultures established from produced water from Marcellus Shale wells located in northcentral Pennsylvania. These cultures were dominated by anaerobic halophilic bacteria from the genus Halanaerobium . Dissolved Ba was determined by ICP-OES and barite surfaces were investigated by SEM and AFM. Our results reveal that: 1) higher amounts of barium (up to ∼5 × ) are released from barite in the presence of Halanaerobium cultures compared to brine controls after 30 days of reaction, 2) etch pits that develop on the barite (001) surface in the presence of Halanaerobium exhibit a morphology that is distinct from those that form during control experiments without bacteria, 3) etch pits that develop in the presence of Halanaerobium exhibit a morphology that is similar to the morphology of etch pits formed in the presence of strong organic chelators, EDTA and DTPA, and 4) experiments using dialysis membranes to separate barite from bacteria suggest that direct contact between the two is not required in order to promote dissolution. These results suggest that Halanaerobium increase the rate of barite dissolution in anoxic and high ionic strength solutions. Additionally, the increase in rate occurs without direct microbe-mineral contact suggesting that metabolites secreted by the bacteria may be responsible for promotion of dissolution. The findings of this study have implications for understanding barium cycling in marine/hypersaline environments, release of barium (and associated radium) from waste solids generated from energy and mining industries, as well as potential for developing new anti-scaling chemicals.

Applied Geochemistry↗