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Dive into the research topics where Jonathan B. Ajo-Franklin is active.

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Featured researches published by Jonathan B. Ajo-Franklin.


Geophysics | 2007

Applying compactness constraints to differential traveltime tomography

Jonathan B. Ajo-Franklin; Burke J. Minsley; Thomas M. Daley

Tomographic imaging problems are typically ill-posed and often require the use of regularization techniques to guarantee a stable solution. Minimization of a weighted norm of model length is one commonly used secondary constraint. Tikhonov methods exploit low-order differential operators to select for solutions that are small, flat, or smooth in one or more dimensions. This class of regularizing functionals may not always be appropriate, particularly in cases where the anomaly being imaged is generated by a nonsmooth spatial process. Time-lapse imaging of flow-induced velocity anomalies is one such case; flow features are often characterized by spatial compactness or connectivity. By performing inversions on differenced arrival time data, the properties of the time-lapse feature can be directly constrained. We develop a differential traveltime tomography algorithm whichselects for compact solutions, i.e., models with a minimum area of support, through application of model-space iteratively reweighted leas...


Environmental Science & Technology | 2014

Pore-scale controls on calcite dissolution rates from flow-through laboratory and numerical experiments.

Sergi Molins; David Trebotich; Li Yang; Jonathan B. Ajo-Franklin; Terry J. Ligocki; Chaopeng Shen; Carl I. Steefel

A combination of experimental, imaging, and modeling techniques were applied to investigate the pore-scale transport and surface reaction controls on calcite dissolution under elevated pCO2 conditions. The laboratory experiment consisted of the injection of a solution at 4 bar pCO2 into a capillary tube packed with crushed calcite. A high resolution pore-scale numerical model was used to simulate the experiment based on a computational domain consisting of reactive calcite, pore space, and the capillary wall constructed from volumetric X-ray microtomography images. Simulated pore-scale effluent concentrations were higher than those measured by a factor of 1.8, with the largest component of the discrepancy related to uncertainties in the reaction rate model and its parameters. However, part of the discrepancy was apparently due to mass transport limitations to reactive surfaces, which were most pronounced near the inlet where larger diffusive boundary layers formed around grains and in slow-flowing pore spaces that exchanged mass by diffusion with fast flow paths. Although minor, the difference between pore- and continuum-scale results due to transport controls was discernible with the highly accurate methods employed and is expected to be more significant where heterogeneity is greater, as in natural subsurface materials.


Proceedings of SPIE | 2012

X-ray micro-tomography at the Advanced Light Source

Alastair A. MacDowell; Dula Parkinson; A. Haboub; E. Schaible; J. Nasiatka; C. A. Yee; J. R. Jameson; Jonathan B. Ajo-Franklin; Craig R. Brodersen; Andrew J. McElrone

The X-ray micro-Tomography Facility at the Advanced Light Source has been in operation since 2004. The source is a superconducting bend magnet of critical energy 11.5 keV; photon energy coverage is 8-45 KeV in monochromatic mode, and a filtered white light option yields useful photons up to 50 keV. A user-friendly graphical user interface allows users to collect tomographic and radiographic data sets with options including tiled and time series data sets. We will focus on recent projects that utilize sample environments for in-situ imaging. These environments include a high pressure triaxial flow cell which has allowed study of supercritical CO2 transport through brine-saturated sandstone at pressures typical of in-situ conditions for subsurface CO2 sequestration and water transportation within live plants.


Geochemical Transactions | 2011

Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation

Yuxin Wu; Jonathan B. Ajo-Franklin; Nicolas Spycher; Susan S. Hubbard; Guoxiang Zhang; Kenneth H. Williams; Joanna Taylor; Yoshiko Fujita; Robert W. Smith

Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic) sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT), and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes promoted through NH4+ production during urea hydrolysis were incorporated in the model and captured critical changes in the major metal species. The electrical phase increases were potentially due to ion exchange processes that modified charge structure at mineral/water interfaces. Our study revealed the potential of geophysical monitoring for geochemical changes during urea hydrolysis and the advantages of combining multiple approaches to understand complex biogeochemical processes in the subsurface.


Geophysics | 2008

Redatuming through a salt canopy and target-oriented salt-flank imaging

Rongrong Lu; Mark E. Willis; Xander Campman; Jonathan B. Ajo-Franklin; M. Nafi Toksöz

We describe a new shortcut strategy for imaging the sediments and salt edge around a salt flank through an overburden salt canopy. We tested its performance and capabilities on 2D synthetic acoustic seismic data from a Gulf of Mexico style model. We first redatumed surface shots, using seismic interferometry, from a walkaway vertical seismic profile survey as if the source and receiver pairs had been located in the borehole at the positions of the receivers. This process creates effective downhole shot gathers by completely moving surface shots through the salt canopy, without any knowledge of overburden velocity structure. After redatuming, we can apply multiple passes of prestack migration from the reference datum of the bore-hole. In our example, first-pass migration, using only a simple vertical velocity gradient model, reveals the outline of the salt edge. A second pass of reverse-time, prestack depth migration using full two-way wave equation was performed with an updated velocity model that consisted of the velocity gradient and salt dome. The second-pass migration brings out dipping sediments abutting the salt flank because these reflectors were illuminated by energy that bounced off the salt flank, forming prismatic reflections. In this target-oriented strategy, the computationally fast redatuming process eliminates the need for the traditional complex process of velocity estimation, model building, and iterative depth migration to remove effects of the salt canopy and surrounding overburden. This might allow this strategy to be used in the field in near real time.


Ground Water | 2011

Hydrogeophysical methods for analyzing aquifer storage and recovery systems

Burke J. Minsley; Jonathan B. Ajo-Franklin; Amitabha Mukhopadhyay; Frank Morgan

Hydrogeophysical methods are presented that support the siting and monitoring of aquifer storage and recovery (ASR) systems. These methods are presented as numerical simulations in the context of a proposed ASR experiment in Kuwait, although the techniques are applicable to numerous ASR projects. Bulk geophysical properties are calculated directly from ASR flow and solute transport simulations using standard petrophysical relationships and are used to simulate the dynamic geophysical response to ASR. This strategy provides a quantitative framework for determining site-specific geophysical methods and data acquisition geometries that can provide the most useful information about the ASR implementation. An axisymmetric, coupled fluid flow and solute transport model simulates injection, storage, and withdrawal of fresh water (salinity ∼500 ppm) into the Dammam aquifer, a tertiary carbonate formation with native salinity approximately 6000 ppm. Sensitivity of the flow simulations to the correlation length of aquifer heterogeneity, aquifer dispersivity, and hydraulic permeability of the confining layer are investigated. The geophysical response using electrical resistivity, time-domain electromagnetic (TEM), and seismic methods is computed at regular intervals during the ASR simulation to investigate the sensitivity of these different techniques to changes in subsurface properties. For the electrical and electromagnetic methods, fluid electric conductivity is derived from the modeled salinity and is combined with an assumed porosity model to compute a bulk electrical resistivity structure. The seismic response is computed from the porosity model and changes in effective stress due to fluid pressure variations during injection/recovery, while changes in fluid properties are introduced through Gassmann fluid substitution.


Journal of Geophysical Research | 2010

On the complex conductivity signatures of calcite precipitation

Yuxin Wu; Susan S. Hubbard; Kenneth H. Williams; Jonathan B. Ajo-Franklin

On the complex conductivity signatures of calcite precipitation Yuxin Wu 1 , Susan Hubbard 1 , Kenneth Hurst Williams 1 , Jonathan Ajo-Franklin 1 1. Earth Sciences Division, Lawrence Berkeley National Laboratory, MS 90-1116, 1 Cyclotron Road, Berkeley, CA 94720 Abstract Calcite is a mineral phase that frequently precipitates during subsurface remediation or geotechnical engineering processes. This precipitation can lead to changes in the overall behavior of the system, such as flow alternation and soil strengthening. Because induced calcite precipitation is typically quite variable in space and time, monitoring its distribution in the subsurface is a challenge. In this research, we conducted a laboratory column experiment to investigate the potential of complex conductivity as a mean to remotely monitor calcite precipitation. Calcite precipitation was induced in a glass bead (3 mm)-packed column through abiotic mixing of CaCl 2 and Na 2 CO 3 solutions. The experiment continued for 12 days with a constant precipitation rate of ~0.6 milimole/day. Visual observations and Scanning Electron Microscope (SEM) imaging revealed two distinct phases of precipitation: an earlier phase dominated by well distributed, discrete precipitates and a later phase characterized by localized precipitate aggregation and associated pore clogging. Complex conductivity measurements exhibited polarization signals that were characteristic of both phases of calcite precipitation, with the precipitation volume and crystal size controlling the overall polarization magnitude and relaxation time constant. We attribute the observed responses to polarization at the electrical double layer (EDL) surrounding calcite crystals. Our experiment illustrates the potential of electrical methods for characterizing the distribution and aggregation state of nonconductive minerals like calcite. Advancing our ability to quantify geochemical transformations using such non-invasive methods is expected to facilitate our understanding of complex processes associated with natural subsurface systems as well as processes induced through engineered treatments (such as environmental remediation and carbon sequestration).


Environmental Science & Technology | 2016

A 2.5D Reactive Transport Model for Fracture Alteration Simulation.

Hang Deng; Sergi Molins; Carl I. Steefel; Donald J. DePaolo; Marco Voltolini; Li Yang; Jonathan B. Ajo-Franklin

Understanding fracture alteration resulting from geochemical reactions is critical in predicting fluid migration in the subsurface and is relevant to multiple environmental challenges. Here, we present a novel 2.5D continuum reactive transport model that captures and predicts the spatial pattern of fracture aperture change and the development of an altered layer in the near-fracture region. The model considers permeability heterogeneity in the fracture plane and updates fracture apertures and flow fields based on local reactions. It tracks the reaction front of each mineral phase and calculates the thickness of the altered layer. Given this treatment, the model is able to account for the diffusion limitation on reaction rates associated with the altered layer. The model results are in good agreement with an experimental study in which a CO2-acidified brine was injected into a fracture in the Duperow Dolomite, causing dissolution of calcite and dolomite that result in the formation of a preferential flow channel and an altered layer. With an effective diffusion coefficient consistent with the experimentally observed porosity of the altered layer, the model captures the progressive decrease in the dissolution rate of the fast-reacting mineral in the altered layer.


Applied and Environmental Microbiology | 2015

Microbial Growth under Supercritical CO2

Kyle C. Peet; Adam Joshua Ehrich Freedman; Hector H. Hernandez; Vanya Britto; Chris Boreham; Jonathan B. Ajo-Franklin; Janelle R. Thompson

ABSTRACT Growth of microorganisms in environments containing CO2 above its critical point is unexpected due to a combination of deleterious effects, including cytoplasmic acidification and membrane destabilization. Thus, supercritical CO2 (scCO2) is generally regarded as a sterilizing agent. We report isolation of bacteria from three sites targeted for geologic carbon dioxide sequestration (GCS) that are capable of growth in pressurized bioreactors containing scCO2. Analysis of 16S rRNA genes from scCO2 enrichment cultures revealed microbial assemblages of varied complexity, including representatives of the genus Bacillus. Propagation of enrichment cultures under scCO2 headspace led to isolation of six strains corresponding to Bacillus cereus, Bacillus subterraneus, Bacillus amyloliquefaciens, Bacillus safensis, and Bacillus megaterium. Isolates are spore-forming, facultative anaerobes and capable of germination and growth under an scCO2 headspace. In addition to these isolates, several Bacillus type strains grew under scCO2, suggesting that this may be a shared feature of spore-forming Bacillus spp. Our results provide direct evidence of microbial activity at the interface between scCO2 and an aqueous phase. Since microbial activity can influence the key mechanisms for permanent storage of sequestered CO2 (i.e., structural, residual, solubility, and mineral trapping), our work suggests that during GCS microorganisms may grow and catalyze biological reactions that influence the fate and transport of CO2 in the deep subsurface.


Frontiers in Microbiology | 2014

Isotopic insights into microbial sulfur cycling in oil reservoirs

Christopher G. Hubbard; Yiwei Cheng; Anna Engelbrekston; Jennifer L. Druhan; Li Li; Jonathan B. Ajo-Franklin; John D. Coates; Mark E. Conrad

Microbial sulfate reduction in oil reservoirs (biosouring) is often associated with secondary oil production where seawater containing high sulfate concentrations (~28 mM) is injected into a reservoir to maintain pressure and displace oil. The sulfide generated from biosouring can cause corrosion of infrastructure, health exposure risks, and higher production costs. Isotope monitoring is a promising approach for understanding microbial sulfur cycling in reservoirs, enabling early detection of biosouring, and understanding the impact of souring. Microbial sulfate reduction is known to result in large shifts in the sulfur and oxygen isotope compositions of the residual sulfate, which can be distinguished from other processes that may be occurring in oil reservoirs, such as precipitation of sulfate and sulfide minerals. Key to the success of this method is using the appropriate isotopic fractionation factors for the conditions and processes being monitored. For a set of batch incubation experiments using a mixed microbial culture with crude oil as the electron donor, we measured a sulfur fractionation factor for sulfate reduction of −30‰. We have incorporated this result into a simplified 1D reservoir reactive transport model to highlight how isotopes can help discriminate between biotic and abiotic processes affecting sulfate and sulfide concentrations. Modeling results suggest that monitoring sulfate isotopes can provide an early indication of souring for reservoirs with reactive iron minerals that can remove the produced sulfide, especially when sulfate reduction occurs in the mixing zone between formation waters (FW) containing elevated concentrations of volatile fatty acids (VFAs) and injection water (IW) containing elevated sulfate. In addition, we examine the role of reservoir thermal, geochemical, hydrological, operational and microbiological conditions in determining microbial souring dynamics and hence the anticipated isotopic signatures.

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Thomas M. Daley

Lawrence Berkeley National Laboratory

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Shan Dou

Lawrence Berkeley National Laboratory

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Barry M. Freifeld

Lawrence Berkeley National Laboratory

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Jil T. Geller

Lawrence Berkeley National Laboratory

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Marco Voltolini

Lawrence Berkeley National Laboratory

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Craig Ulrich

Lawrence Berkeley National Laboratory

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John E. Peterson

Lawrence Berkeley National Laboratory

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Yuxin Wu

Lawrence Berkeley National Laboratory

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Kenneth H. Williams

Lawrence Berkeley National Laboratory

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Michelle Robertson

Lawrence Berkeley National Laboratory

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