Name: Reservoir Condition Pore-scale Imaging of Multiple Fluid Phases Using X-ray Microtomography (Video) | JoVE Journal
Uploaded: 2015-02-25T14:00:00.000+00:00
Duration: 8 min 2 s
Description: Learn reservoir condition micro CT imaging for multiphase flow analysis using carbonate rock samples. This method visualizes capillary trapping of supercritical carbon dioxide to advance carbon capture and enhanced oil recovery research.

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5 minutes

We gratefully acknowledge funding from the Qatar Carbonates and Carbon Storage Research Centre (QCCSRC), provided jointly by Qatar Petroleum, Shell, and Qatar Science &#38; Technology Park. We also acknowledge funding from the Imperial College Consortium on Pore-Scale Modelling.

1. Imaging Strategy Design
<ol>
	<li>In order to predict the imaging performance of different solute choices for the brine, calculate the x-ray spectrum of the incident x-rays29-31. Include the impact of the core-holder, core assembly and confining fluids on x-ray spectrum. An example incident x-ray spectrum using an acceleration voltage of 80 kV and electron current of 87 &#181;A is shown in Figure 1.</li>
	<li>Compare this spectrum to the transmission factors of the sample containing different pore-fluids. Simulate changes in the transmission factor due to changes in the pore-fluid using the Beer-Lambert law, assuming an effective optical length of the species within the sample, and calculated x-ray attenuation coefficients (Figure 3)32. Determine the overall transmission factor by integrating over all incident x-ray energies. An example of the resulting effective transmission factors for the rock matrix and pore-space material, and the changes in transmission factors relative to the case when the pore-space is filled with vacuum can be seen in Table 1.</li>
	<li>Choose a brine solute and concentration such that the change in transmission factor associated with brine is approximately half the change in transmission factor associated with the solid. This will maximize three phase contrast in the reconstructed image. Weigh out the required amount of salt (7% (w/w) KI was used for the experiment from which the representative results were taken) and vigorously mix with deionized water.
	<ol>
		<li>Alternatively, if a specific brine composition is desired, change the x-ray source acceleration voltage to change the spectrum of the incident x-rays.</li>
	</ol>
	</li>
</ol>
2. Assembly of Equipment and Cell
<ol>
	<li>Assemble the equipment as shown below in Figure 2. Use PEEK flowlines to reduce lateral sample load on the flow cell. Test each connection carefully for any fluid leaks.
	<ol>
		<li>Place the brine, of composition decided during steps 1.1-1.3, in the base of the reactor. Wrap the flexible heater around the flow cell.</li>
	</ol>
	</li>
	<li>Construct metal end fittings. Remove the thread from the 1/8&#8221; end of a 1/16&#8221; to 1/8&#8221; reducer fitting. Then cut small grooves into the face of the 1/8&#8221; end of the fitting to distribute the injected CO2 over the entire face of the core.</li>
	<li>Pass the high pressure thermocouple through the metal end parts of the micro-flow cell and seal using &#188;&#8221; ferrules and nut, so the hot junction of the thermocouple sits adjacent to the inlet face of the core, within the confining annulus of the cell.</li>
	<li>Drill desired sample into a core 6.5 mm in diameter and 30 mm to 50 mm in length. Grind down the ends of the core flat, to ensure a good connection with the metal end pieces. Wrap this core in aluminum foil then place within a flouro-polymer elastomer sleeve.
	<ol>
		<li>Connect the ends of the elastomer sleeve to the metal end fittings. Add another wrap of aluminum foil to the exterior of the elastomer sleeve before placing the hot junction of the thermocouple next to the confining annulus of the cell and adding a final wrap of aluminum foil. This forms the core assembly (Figure 4).</li>
	</ol>
	</li>
	<li>Assemble the micro-flow cell with the core assembly sealed within it and connect the cell to the stage within the micro-CT enclosure (Figure 5) using a clamp mounted on top of the rotational CT stage.</li>
</ol>
3. System Pressurization
<ol>
	<li>Close all valves apart from valve 1, 2 and 3, as defined in Figure 3. Load CO2 from the cylinder into pump 1 and the reactor, then close valve 1. Slowly raise the temperature and pressure within the reactor to that desired for the pore fluid during the experiment.</li>
	<li>Vigorously mix the reactor for at least 12 hr to ensure all phases are in chemical equilibrium prior to injection.</li>
	<li>Open valve 14 and load the confining fluid into pump 3. Close valve 14. Open valves 12 and 13. Pressurize the confining annulus of the cell to at least 10% higher than the proposed pore-fluid pressure.</li>
	<li>Open valve 11. Load brine into pump 2. Close valve 11 and open valves 9, 8 and 6.
	<ol>
		<li>Slowly pressurize the pore-space of the rock until it is at the desired pore-fluid pressure, filling the pore-space of the sample with brine that has not been equilibrated with scCO2.</li>
	</ol>
	</li>
	<li>Open valve 4. Flush more than 1,000 pore volumes of equilibrated brine through the core by refilling pump 2 at a constant flow rate. Pore volume is found by multiplying the core volume by the porosity found using helium porosimetry. 
	NOTE: This will miscibly displace the un-equilibrated brine, ensuring 100% initial brine saturation and creating conditions in the core akin to the subsurface conditions in an aquifer at a point slightly ahead of the front of a scCO2 plume.</li>
</ol>
4. Fluid Flow and Image Acquisition
<ol>
	<li>Pass through 10 pore volumes (around 1 ml) of scCO2 through the core at very low flow rates (1.67 &#215; 10-9 m3/sec), ensuring a low capillary number of around 10-6. Continually take 2D projections in order to accurately measure the total injected volume by observing the point when scCO2 displaces brine in the pore space.</li>
	<li>Pass through 10 pore volumes (around 1 ml) of equilibrated brine through the core at the same low flow rate, causing scCO2 to become trapped as a residual phase in the pore-space.</li>
	<li>After steps 4.1 or 4.2, take scans of the sample to image drainage or imbibition respectively. Use a voxel size such that the entire diameter of the core fits within the field of view.</li>
	<li>Reconstruct the scans using a tomographic reconstruction program. To scan the entire length of the core while retain a small voxel size, reconstruct composite volumes by stitching together multiple overlapping sections, acquired sequentially. 
	NOTE: Each section required around 400 projections, taking 15-20 min to acquire, so the scanning of an entire composite volume took around 90 min.</li>
</ol>
5. Image Processing and Segmentation
<ol>
	<li>Apply a non-local means edge preserving filter33,34 to the dataset and correct the images for any beam hardening or softening artifacts created during image reconstruction by modeling these artifacts as radially symmetric Gaussian functions35.</li>
	<li>Segment the data (turn the greyscale information into a binary representation of the CO2 within the image) by the use of a watershed algorithm with a seed generated using a 2D histogram36, treating the CO2 as one phase and the brine and the rock together as the other phase.</li>
	<li>Analyze this segmented image to find both the total number of CO2 voxels and also the sizes of each connected cluster of residual CO2.</li>
</ol>

The authors have nothing to disclose.

The most critical steps for successful imaging of multiphase fluids at elevated pressures and temperatures are: 1) The successful isolation of the pore fluid from the surrounding confining fluid; 2) the effective equilibration of the fluids and rock prior to injection; 3) effective temperature control throughout the experiment; and 4) the effective segmentation of the resulting images.
The use of the aluminum wraps is critical for the successful isolation of the pore-fluid from the surrounding confining fluid as in its absence diffusive exchange across the sleeve is rapid, and saturation within the core does not remain constant for the duration of the scan. This problem can also be evident when fluid remains in the PEEK flowlines for extended periods of time (&#62; 2 hr) prior to injection into the core in step 4.1 and 4.2. Once again, CO2 diffusively exchanges across the plastic, causing the brine to desaturate. If this desaturated brine is injected into the core, the saturation in the core will decrease as residual clusters are dissolved by the injected brine.
Other methods for the equilibration of fluids and rocks, including fluid recirculation50, have been proposed in the literature. These methods increase the complexity of the experimental setup, which in turn would have increased the amount of time for each experiment, which would have in turn increased the likelihood that the brine in flow lines would have diffusively desaturated.
Effective temperature control is essential, and the presence of a thermocouple within the confining annulus of the flow cell is critical for this. Temperature is only measured at a single point, meaning there may be some gradient across the sample, leading to solubility imbalance and dissolution or exsolution. This can be minimized by locating the hot junction of the thermocouple as close as possible to the inlet face of the rock core.
The effective segmentation of the resulting images can be a real challenge with these systems, as the segmentation of images containing a partial saturation of multiple fluids is significantly more challenging that the segmentation of dry images, so the use of simple grey-scale universal thresholding is insufficient51. The use of watershed segmentation not only gives the most reliable results, compared to other algorithms in the literature, but is also the most effective at dealing with ring and partial volume artifacts35.
One of the most significant limitations of this technique is that it can only access the macro-pore space of a rock. The microporosity (on scales smaller than the image resolution) remains inaccessible, and may be important for multiphase flow. Higher resolutions reveal a greater proportion of these parts of pore space, but also correspond to a decrease in the field of view. The applicability of the technique to a specific rock type could be addressed by comparing the resolution of the scan to the pore throat size distribution obtained using independent method such as mercury injection capillary pressure.
This method is a leading technique for the pore-scale imaging of multiple fluids at reservoir conditions in realistic systems, with existing applications including a cross comparative study of capillary trapping24 and the measurement of contact angle26, and the method is easily applicable to a large range of porous systems. Future work could study, at the pore scale, a wide variety of single phase and multiphase flow in porous media problems at conditions representative of subsurface aquifers, oil and gas fields and other deep geological systems.

Carbon Capture and Storage is the process where CO2 is captured from large point sources and stored in porous rock, displacing resident brines so that it remains in the subsurface for hundreds to thousands of years1. The CO2 resides in the subsurface as a dense super-critical phase (scCO2), with properties radically different to CO2 at ambient conditions. There are four principal mechanisms by which scCO2 might be immobilized in the subsurface: stratigraphic, solubility, mineral and residual trapping. Stratigraphic trapping is where CO2 is held underneath impermeable seal rocks; solubility trapping is where CO2 dissolves into the resident brine surrounding the injected CO22-4; mineral trapping is where carbonate mineral phases are precipitated into the rock5; and residual or capillary trapping is where CO2 is held by surface forces as tiny droplets (ganglia) in the pore-space of the rock6. This can occur either naturally, by the migration of the CO2 plume7-9, or can be induced by the injection of chase brines10. In order to understand the processes governing the flow and trapping of this CO2 in the subsurface a new suite of experiments must be conducted, harnessing new advances in technology to better understand the fundamental physics associated with multi-phase flow.
X-ray microtomography has developed as a technique over the past 25 years from early attempts to visualize both dry geological samples11 and multiple fluid phases12 to the primary method for the non-invasive imaging of rock cores, both for modeling purposes and for experimental implementation13-15. Because microtomography is non-invasive, it has the ability to study systems at representative conditions, which is particularly attractive for the CO2-brine-rock system, as the multiphase flow behavior of scCO2 is highly dependent on thermo-physical properties, such as interfacial tension and contact angle, which are in turn a strong function of system conditions such as temperature, pressure and salinity16-18. In such a complex system, with such an extensive and poorly understood set of inter-dependent variables, experiments using idealized pore structures19 or analogue fluids20,21 may not be applicable to flow processes in the subsurface. Imaging multiple fluids at conditions representative of a prospective CO2 injection formation has, however, remained a challenge22. In this study we outline a methodology for the examination of multi-fluid behavior at reservoir conditions, focusing on the examination of capillary trapping23,24. This will include the designing of an imaging strategy, the assembly of the fluid cell, the injection strategy and subsequent image processing.
The experimental examination of pore-scale multiphase flow behavior in real rock systems focuses on the imaging of partially saturated rock cores after both non-wetting phase injection (drainage) and wetting phase injection (imbibition). These fluids are injected by connecting the cores to fluid injection pumps using flexible flow lines, while confining the core using a Hassler-type coreholder design25. To successfully image the in-situ arrangement of scCO2 and brine, a novel and highly sensitive experimental setup was used, primarily focusing on the use of a high resolution x-ray microscope23,24,26. The requirements for conducting experiments at elevated temperatures and pressures are very stringent, and require recent developments in both materials technology and micro-CT facilities. The key requirements that have to be fulfilled are that any core/sample holder needs to be able to withstand high pressure high temperature (HPHT) conditions while remaining sufficiently x-ray transparent to allow for effective imaging. Lab-based instruments impose an additional constraint, as the core-holder must be small enough such that the x-ray source can be placed close to the sample and that sufficiently large geometric x-ray magnification can be achieved such that the pore space is effectively resolved. Although this constraint has been relaxed somewhat with the introduction of secondary optics in newer lab-based micro-CT machines, it has not been completely removed, especially if rapid acquisition times are desired, as higher optical magnifications tend to increase the time required to acquire images.
Experiments with soluble fluids provide an additional challenge when using lengthy acquisition times, as CO2 will diffuse through the polymeric portions of the experimental assembly, reducing the in-situ fluid saturation. All these issues meant that scan times longer than around 2 hr were impractical. In order to keep scan times below this requirement, particularly stringent for lab based sources, the core-holder must be around 1 cm in diameter. A larger coreholder size would have required the detector to be much further from the source to achieve the same geometric magnification, reducing the x-ray flux incident on the detector and therefore increasing required projection exposure times. The flow cell used in these experiments was based on a traditional Hassler cell design, built around a carbon fiber sleeve, with a sleeve design similar to that used by Iglauer et al.27, but with two significant alterations: 1) The carbon fiber composite used in the sleeve manufacture was changed from T700 fibers, with a stiffness of 230 GPa, to M55 fibers, with a stiffness of 550 GPa. This not only reduced the amount of sample movement during tomography acquisition, but also increased the maximum working pressure of the cell from 20 MPa to 50 MPa. 2) The sleeve has been elongated from 212 mm to 262 mm to allow the source and detector to be as close to the sample as possible.
A major experimental shortcoming in the first study to use micro-CT to examine CO2 at reservoir conditions was the use of metal lines to control the flow to and from the core-holder27. As the sample is rotated relative to the pumps, the flow lines also need to be rotated. Stiff flow lines can cause the sample to move, reducing effective image resolution or making some or all of the dataset unusable. To prevent this we replaced all the flow lines close to the rotation stage with flexible polyether ether ketone (PEEK) tubing. These flow lines were flexible, providing very small lateral forces (load) to the core-holder during acquisition. We also attached the flow lines to valves attached to the sample stage, rather than attaching the flow lines to the coreholder. This meant that any existing flow-line load was transmitted directly to the stage, rather than to the sample, reducing the probability of sample motion. A major disadvantage of using the PEEK tubing was that CO2 was able to slowly diffuse through it, over a timescale of around 24 hr. This meant that CO2 saturated brine left in the flow lines would gradually desaturate.
Another major experimental shortcoming of previous studies was inaccurate control of temperature. This can impact results in a number of ways. Firstly, temperature is a strong control on both interfacial tension and contact angle16-18. Moreover, the solubility of both scCO2 and carbonate rock in brine is also highly temperature dependent28. Solubility control is critical, as when scCO2 is injected into a saline carbonate aquifer it will dissolve into the resident brine, forming a highly reactive carbonic acid, which will in turn start to dissolve any calcite present. Any inaccuracy in solubility control can therefore lead to scCO2 dissolution/exsolution or solid dissolution/precipitation.
Previous studies27 used a heated confining fluid to heat the coreholder; however this was problematic. It has the disadvantages associated with the difficulty of accurately maintaining a constant confining pressure using a recirculating water supply, requiring extra heating baths for that supply. Furthermore, this system only maintains an accurate control of temperature at the point of the heating bath (not at the point of the core holder, and the confining fluid would cool between the water bath and the core holder). It also requires both an inlet and an outlet port for the confining fluid, increasing the number of fluid lines attached to the coreholder and so increasing flow line load.
Instead of using a heated confining fluid, a flexible heating jacket was used to surround the core holder. This very simple heating method resulted in very little coreholder load, and allowed for the precise and accurate heating. An extremely thin polyimide heating film was used, in order to minimize sample size. The construction of this film consists of an etched copper foil element 0.0127 mm thick, encapsulated between two layers of 0.0508 mm polyimide film. The copper elements present in the jacket did not noticeably affect image quality. Temperature was measured using a thermocouple sitting in the confining annulus of the cell. It was positioned on the outside of the confining sleeve, as close as possible to the core, ensuring an accurate, reliable and stable reading of the pore-fluid temperature. The thermocouple and heating film were connected to a custom built Proportional Integral Derivative (PID) controller, and temperatures were controlled within &#177; 1 &#176;C.
To maintain complete control over inter-phase solubility, and represent conditions present in the aquifer far away from the injection site, prior to injection the brine was equilibrated with scCO2 by vigorously mixing the two fluids together with small particles (1-2 mm) of the host rock in a stirred and heated reactor. All wetted components within this reactor are made of Hastelloy to minimize corrosion. The reactor contains a filtered dip tube to allow for denser fluid to be extracted from the base of the reactor (brine) and less dense fluid to be extracted from the top of the reactor (scCO2). High pressure syringe pumps were used to maintain pressure and control flow in the pore-space of the rock and in the reactor, with a displacement accuracy of 25.4 nl. The experimental apparatus used in this study is shown in Figure 1. The ionic salt used for the experiment from which the representative results were drawn was Potassium Iodide (KI), as it has a high atomic weight and so a high x-ray attenuation coefficient, making it an effective contrast agent. Less attenuating salts (such as NaCl) or mixtures could be used, however larger salinities would be required to achieve the same x-ray attenuation.

<table><tbody><tr><td>High Pressure Syringe Pump</td><td>Teledyne ISCO</td><td>1000D</td><td></td></tr><tr><td>Parr Reactor</td><td>Parr Instrument Company</td><td>4547A - hastelloy</td><td></td></tr><tr><td>PEEK Tubing</td><td>Kinesis</td><td>1560xL</td><td></td></tr><tr><td>Potassium Iodide Salt</td><td>Sigma Aldrich</td><td>30315-1KG</td><td></td></tr><tr><td>Carbon Dioxide</td><td>BOC</td><td>CO2 - size E</td><td></td></tr><tr><td>Thermocouple</td><td>Omega Engineering</td><td>KMTSS-IM300U-150</td><td></td></tr><tr><td>Kapton Flexible Heater</td><td>Omega Engineering</td><td>KH-112/10-P</td><td></td></tr><tr><td>X-Ray Microscope</td><td>Zeiss</td><td>Versa XRM 500</td><td></td></tr><tr><td>Snoop Leak Detector</td><td>Swagelok</td><td>MS-SNOOP-8OZ</td><td></td></tr><tr><td>Flouro-Elastomer Polymer (Viton) Sleeve</td><td>Fisher Scientific</td><td>11572583</td><td></td></tr><tr><td>Micro-CT Coreholder</td><td>Airborne Composites</td><td>262mm Coreholder</td><td>Constructed in conjunction with Imperial College</td></tr><tr><td>Tomographic program</td><td>Zeiss</td><td>XM-Reconstructor</td><td></td></tr><tr><td>ImageJ - image processing</td><td>NIH</td><td>ImageJ</td><td></td></tr><tr><td>Matlab</td><td>Mathworks</td><td>Matlab</td><td>Used for regression analysis</td></tr><tr><td>Avizo</td><td>FEI</td><td>Avizo</td><td></td></tr></tbody></table>

reservoir condition pore-scale imaging of multiple fluid phases using x-ray microtomography

Reservoir Condition Pore-scale Imaging of Multiple Fluid Phases Using X-ray Microtomography

X-ray microtomography was used to image, at a resolution of 6.6 &#181;m, the pore-scale arrangement of residual carbon dioxide ganglia in the pore-space of a carbonate rock at pressures and temperatures representative of typical formations used for CO2 storage. Chemical equilibrium between the CO2, brine and rock phases was maintained using a high pressure high temperature reactor, replicating conditions far away from the injection site. Fluid flow was controlled using high pressure high temperature syringe pumps. To maintain representative in-situ conditions within the micro-CT scanner a carbon fiber high pressure micro-CT coreholder was used. Diffusive CO2 exchange across the confining sleeve from the pore-space of the rock to the confining fluid was prevented by surrounding the core with a triple wrap of aluminum foil. Reconstructed brine contrast was modeled using a polychromatic x-ray source, and brine composition was chosen to maximize the three phase contrast between the two fluids and the rock. Flexible flow lines were used to reduce forces on the sample during image acquisition, potentially causing unwanted sample motion, a major shortcoming in previous techniques. An internal thermocouple, placed directly adjacent to the rock core, coupled with an external flexible heating wrap and a PID controller was used to maintain a constant temperature within the flow cell. Substantial amounts of CO2 were trapped, with a residual saturation of 0.203 &#177; 0.013, and the sizes of larger volume ganglia obey power law distributions, consistent with percolation theory.

The results for a single carbonate, Ketton limestone, an oolite from the upper Lincolnshire Limestone Member were analyzed in 3D in order to identify and measure the volume of each unique disconnected ganglion, which was then labeled (Figure 6). All processing was conducted within the Avizo Fire 8.0 and ImageJ programs37.
The segmented partially saturated images were analyzed by counting the number of voxels of residually trapped scCO2 to find the proportion of the rock volume occupied by trapped scCO2 — the capillary trapping capacity. This can then be converted to a residual saturation (Sr) by dividing this value by the porosity as obtained using helium porosimetry. Significant proportions of scCO2 were trapped as a residual saturation, with a residual saturation of 0.203 ± 0.013. This agrees with the results found in previous studies using micro-CT23. Larger core-scale studies of residual trapping in this rock type showed a lower residual saturation of 0.137 ± 0.01238.
The ingress of brine into a scCO2 saturated core is an imbibition process where a wetting fluid (brine) invades each pore, displacing non wetting fluid (scCO2). In a strongly water-wet rock we expect the water to fill areas of the pore space in order of size39,40, trapping disconnected ganglia in the process called snap-off. This process should be percolation like41 so predictions can be made about the size distribution of the isolated clusters. The number n of clusters of volume s (measured in voxels) should scale as , where τ is the Fisher exponent42. Network modeling has shown that in three-dimensional cubic regular lattices the value of this exponent is around τ=2.18943. One natural way of extracting this exponent from real data is to plot the binned quantity, as defined by Dias and Wilkinson41.
<img alt="Equation showing static equilibrium: Ns=Σs'−1s'=sns, relevant for physics calculations." fo:content-width="2in" src="/files/ftp_upload/52440/52440eq1.jpg" data-altupdatedat="1787630408000" data-alt="Equation 1">
which should scale as:
<img alt="Power law equation \(N_s \sim S^{-(\tau-1)}\); mathematical model, data analysis." fo:content-width="2in" src="/files/ftp_upload/52440/52440eq2.jpg" data-altupdatedat="1787630408000" data-alt="Equation 2">
This is then plotted on a log-log plot as a function of s (Figure 7), showing power-law behavior for large ganglia, but an under-representation of smaller ganglia compared to the power law model. The exponent was calculated by excluding ganglia smaller than 105 voxels (approximately the start of the power-law behavior) and performing Levenberg-Marquardt regression44,45 using a least absolute residual robust fitting algorithm46,47. This was performed using a commercial software package. The Fisher exponent for this system was 2.287 ± 0.009, close to the theoretical value of 2.189, indicating that imbibition in this system is indeed percolation like. More generally these results confirm conclusions in larger core-flood experiments38,48,49 that scCO2 acts as the non-wetting phase in carbonates.
<img alt="CO2-brine reactor flow diagram with pumps, valves, flow lines, X-ray enclosure for fluid analysis." src="/files/ftp_upload/52440/52440fig1.jpg" data-altupdatedat="1787630408000" data-alt="Figure 1"> 
Figure 1. Experimental apparatus, showing the pumps, valves and reactor used to control flow and the seating of the coreholder within the micro-CT enclosure. <a href="https://www.jove.com/files/ftp_upload/52440/52440fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="X-ray fluorescence spectrum chart; normalized intensity vs energy; peak analysis for material composition." src="/files/ftp_upload/52440/52440fig2.jpg" data-altupdatedat="1787630408000" data-alt="Figure 2"> 
Figure 2. The normalized energy spectrum for x-rays incident on the core, filtered through the coreholder, confining sleeve and confining fluid. Calculated using SpekCALC29-31.
<img alt="Linear attenuation coefficients vs. photon energy chart; materials: CaCO3, CO2, SiO2; spectroscopic analysis." src="/files/ftp_upload/52440/52440fig3.jpg" data-altupdatedat="1787630408000" data-alt="Figure 3"> 
Figure 3. The linear attenuation coefficients of different fluids and rock materials as a function of photon energy.
<img alt="Thermal insulation setup diagram with aluminum layers, thermocouple, and fluoro-elastomer core." src="/files/ftp_upload/52440/52440fig4.jpg" data-altupdatedat="1787630408000" data-alt="Figure 4"> 
Figure 4. Detail of the core assembly, showing a triple aluminum wrap around the core, preventing diffusive CO2 exchange across the flouro-elastomer sleeve. <a href="https://www.jove.com/files/ftp_upload/52440/52440fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="X-ray spectroscopy setup diagram; core analysis with detector, thermocouple, heating components." src="/files/ftp_upload/52440/52440fig5.jpg" data-altupdatedat="1787630408000" data-alt="Figure 5"> 
Figure 5. Detail of the flow cell, heating apparatus and siting of the core assembly within the flow cell. The thermocouple must be placed as close as possible to the inlet face of the core. <a href="https://www.jove.com/files/ftp_upload/52440/52440fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Granular material simulation diagrams and microscopy images; particle distribution analysis." src="/files/ftp_upload/52440/52440fig6.jpg" data-altupdatedat="1787630408000" data-alt="Figure 6"> 
Figure 6. Image of the carbonate after drainage and imbibition. (A) A 3D rendering of the core after drainage where each non-wetting phase cluster is given a different color. (B-F) A 3D rendering of the core after five imbibition experiments, colored as described for (A). The large range of colors indicates a poorly connected residual phase. (G) A cross-section of the core after drainage. The darkest phase is the scCO2, the intermediate phase is brine and the lightest phase is rock grain. (H) A cross-section of the core after imbibition. <a href="https://www.jove.com/files/ftp_upload/52440/52440fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Log-log graph of ganglion size vs. N(s), linear trend, data analysis in neuroimaging research." src="/files/ftp_upload/52440/52440fig7.jpg" data-altupdatedat="1787630408000" data-alt="Figure 7"> 
Figure 7. The size distribution of the residual ganglia shown in Figure 6.
<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td>Material Filling Porosity</td>
			<td>Vacuum</td>
			<td>CO2</td>
			<td>H2O</td>
			<td>H2O – 7 wt% NaCl</td>
			<td>H2O – 7 wt% KI</td>
			<td>Solid (CaCO3)</td>
		</tr>
		<tr>
			<td>Transmission Factor</td>
			<td>0.25</td>
			<td>0.247</td>
			<td>0.243</td>
			<td>0.242</td>
			<td>0.224</td>
			<td>0.202</td>
		</tr>
		<tr>
			<td>Change in transmission factor relative to vacuum</td>
			<td>N/A</td>
			<td>-0.003</td>
			<td>-0.007</td>
			<td>-0.008</td>
			<td>-0.026</td>
			<td>-0.048</td>
		</tr>
	</tbody>
</table>
Table 1. Summary of results (transmission factor and change in transmission factor relative to the vacuum filled case) from simulation of the x-ray optical properties of the rock and pore-space filling material imaged during this study. Each column represents a different material filling the pore-space of the rock within the coreholder.

We present a methodology for the imaging of multiple fluid phases at reservoir conditions by the use of x-ray microtomography. We show some representative results of capillary trapping in a carbonate rock sample.

X-ray microtomography was used to image, at a resolution of 6.6 &#181;m, the pore-scale arrangement of residual carbon dioxide ganglia in the pore-space ...

The goal of this procedure is to non-invasively image multiple fluid phases in the pore space of rock at realistic conditions of temperature and pressure similar to those occurring in subsurface reservoirs and aquifers. This is accomplished by first assembling the core assembly carefully and placing this within a high pressure, high temperature core holder. The second step is to attach the core holder to the high pressure, high temperature control pumps and reactor using flexible peak tubing.Next, the pressure and temperature in the system erase to that of the representative. Subsurface conditions and fluids are equilibrated and injected into the pore space of the rock. Ultimately, reservoir condition.Micro CT imaging is used to show both the amount and the distribution of carbon dioxide held in place as a trapped residual phase after brine injection. This method can help answer key questions in the field of multiphase flow in porous media, such as determination of residual saturation for capillary trapping and wearability and contact angle measurements. Although this method can provide insights into super critical CO2 brine rock systems with application to carbon capture and storage, it can also be used for hydrocarbon brine rock systems for studying phenomena related to enhanced oil recovery and international resources.Visual demonstration of this method is critical as the sample preparation and core assembly steps are difficult to learn. This is because the relationship between the core assembly, the core, the confining sleeve, and the multiple aluminum wraps is complicated. To begin this procedure, test the connections of the equipment carefully for any fluid leaks.Next place the brine in the base of the reactor. Wrap the flexible heater around the flow cell After that, construct the metal end fittings by removing the thread from the one eighth of an inch end of a one 16th of an inch to a one eighth of an inch reducer fitting. Then cut small grooves into the face of the one eighth of an inch end of the fitting to distribute the injected carbon dioxide over the entire face of the core.Subsequently, pass the high pressure thermocouple through the metal end parts of the microflow cell seal the thermocouple using the quarter inch ferals and nuts, so the hot junction sits adjacent to the in nut face of the core within the confining annulus of the cell L.Next, drill the desired sample into a core of 6.5 millimeters in diameter and 30 millimeters to 50 millimeters in length. R down the ends of the core flat to ensure a good connection with the metal end pieces. Then wrap this core in aluminum foil.Subsequently place it within a fluoro polymer elastomer sleeve. After that, connect the ends of the elastomer sleeve to the metal end fittings. Add another wrap of aluminum foil to the exterior of the elastomer sleeve before placing the hot junction of the thermocouple next to the inlet face of the core, and adding a final wrap of aluminum foil.This forms the core assembly. Now assemble the microflow cell with the core assembly sealed within it. Connect the cell to the stage within the micro CT enclosure using a clamp mounted on top of the rotational CT stage.In this procedure, close all the valves apart from valve one, two, and three. After that, load carbon dioxide from the cylinder into pump one and the reactor. Then close valve one.Slowly raise the temperature and pressure of the reactor to that desired for the pore fluid vigorously. Mix the pore fluid for at least 12 hours to ensure all phases are in chemical equilibrium prior to injection. Next, open valve 14, and load the confining fluid into pump three.Then close it and open valves 12 and 13. Pressurize the confining annulus of the cell to at least 10%higher than the proposed pore fluid pressure. After that, open valve 11.Load the brine into pump two and close it. Subsequently open valves nine, eight and six. Slowly pressurize the pore space of the rock until it is at the desired pore fluid pressure and fill the pore space of the sample with brine that has not been equilibrated with supercritical carbon dioxide.Now, open valve four plus more than 1000 poor volumes of equilibrated brine through the core by refilling pump two at a constant flow rate in this procedure past 10 pore volumes of supercritical carbon dioxide through the core at a very low flow rate, ensuring a low capillary number of around 10 to the minus six continuously. Take 2D projections in order to accurately measure the total injected volume while supercritical carbon dioxide is displacing the brine in the pore space. Pass another 10 volumes of equated brine through the core at the same low flow rate resulting in the trapping of supercritical carbon dioxide as a residual phase in the pore space.After that, take a few scans of the sample to image the drainage or inhibition. Use a voxel size such that the entire diameter of the core fits within the field of view. Then reconstruct the scans using tomographic reconstruction program.Reconstruct the composite volumes by stitching together multiple overlapping sections that are required sequentially. The image shown here is a 3D rendering of the core after drainage where each non-wetting phase cluster is given a different color. These five images show a 3D rendering of the same core after five separate inhibition experiments, whereas the large range of colors indicates a poorly connected residual phase.This is a cross section of the core after drainage. The darkest phase is super critical carbon dioxide. The intermediate phase is brine, and the lightest phase is rock grain, and this is a cross section of the core.After inhibition, the power law scaling of the residual ganglia size distribution is shown here. Once mastered, this technique can be done in around two hours if performed properly. Remember That working with the equipment at high pressure and temperatures can be extremely hazardous, so precautions such as appropriate training and equipment certification must be taken prior to conducting experimental procedure.

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Research

JoVE Journal

Engineering

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