Patent Application
20180171782
This disclosure relates to detecting tracers in a hydrocarbon reservoir.
In a hydrocarbon reservoir, subsurface fluid flow patterns can be analyzed to develop a geological model for the hydrocarbon reservoir. The model can be used to generate one or more parameters that are useful in reservoir resource management, including, for example, well to well connectivity, fluid allocation, fracture locations, swept volumes and residual oil saturations.
The present disclosure describes methods and systems for detecting tracers in a hydrocarbon reservoir. One method includes injecting a multi-modal tracer at a first location in a reservoir, wherein the multi-modal tracer mixes with subsurface fluid in the reservoir; collecting fluid samples at a second location in the reservoir; and analyzing the fluid samples to detect a presence of the multi-modal tracer in the fluid samples. Other implementations of this aspect include corresponding systems and apparatuses.
The foregoing and other implementations can each, optionally, include one or more of the following features, alone or in combination:
A first aspect, combinable with the general implementation, the method further includes determining a subsurface fluid-flow pattern based on the detected presence of the multi-modal tracer.
A second aspect, combinable with any of the previous aspects, wherein the multi-modal tracer comprises a particle loaded with at least two taggants, and each of the at least two taggants is associated with a different detection technique.
A third aspect, combinable with any of the previous aspects, wherein the multi-modal tracer comprises a nanoparticle.
A fourth aspect, combinable with any of the previous aspects, wherein the multi-modal tracer is loaded with at least a fluorescence taggant and a mass spectrometry taggant.
A fifth aspect, combinable with any of the previous aspects, wherein analyzing the fluid samples comprises: determining a first barcode component, wherein the first barcode component represents a fluorescence signal generated using a fluorescence detection technique; determining a second barcode component, wherein the second barcode component represents a mass spectrometry signal generated using a mass spectrometry detection technique; generating a barcode based on the first and the second barcode components; and comparing the generated barcode with a plurality of barcodes to detect the presence of the multi-modal tracer, each of the plurality of barcodes representing a particular multi-modal tracer.
A sixth aspect, combinable with any of the previous aspects, wherein the fluorescence detection technique comprises an upconversion luminescence operation, and the fluorescence taggant comprises an upconverting taggant.
A seventh aspect, combinable with any of the previous aspects, wherein the fluorescence detection technique comprises a time-gated fluorescence spectroscopy technique, and the fluorescence taggant comprises sheathed lanthanide emitters or persistent phosphor materials.
An eighth aspect, combinable with any of the previous aspects, wherein the fluorescence detection technique is used to generate the first barcode component prior to the generation of the second barcode component using the mass spectrometry detection technique.
A ninth aspect, combinable with any of the previous aspects, wherein the mass spectrometry taggant is incorporated in a polymeric nanoparticle.
A tenth aspect, combinable with any of the previous aspects, wherein the mass spectrometry detection technique comprises a Gas Chromatography Mass Spectrometry operation.
An eleventh aspect, combinable with any of the previous aspects, wherein the multi-modal tracer is further loaded with a surface-enhanced Raman spectroscopy (SERS) taggant, and analyzing the fluid samples comprises: determining a third barcode component, wherein the third barcode component represents a SERS signal generated using a SERS detection technique; and wherein the barcode is generated based on the first, the second, and the third barcode components.
A twelfth aspect, combinable with any of the previous aspects, wherein the SERS taggant comprise a thermally stable dye molecule embedded within a nanoparticle.
A thirteenth aspect, combinable with any of the previous aspects, wherein the fluid samples are analyzed in real time at the second location.
A fourteenth aspect, combinable with any of the previous aspects, wherein the subsurface fluid comprises at least one of natural ga, petroleum, connate water, or seawater.
A multi-modal tracer for mixing with subsurface fluid in a reservoir includes: a fluorescence taggant associated with a first barcode component; a mass spectrometry taggant associated with a second barcode component; and wherein the first barcode component and the second barcode component form a barcode that identifies the multi-modal tracer.
The foregoing and other implementations can each, optionally, include one or more of the following features, alone or in combination:
A first aspect, combinable with the general implementation, wherein the fluorescence taggant comprises an upconverting taggant.
A second aspect, combinable with any of the previous aspects, wherein the fluorescence taggant comprises sheathed lanthanide emitters or persistent phosphor materials.
A third aspect, combinable with any of the previous aspects, wherein the mass spectrometry taggant is incorporated in a polymeric nanoparticle.
A fourth aspect, combinable with any of the previous aspects, wherein the multi-modal tracer further comprises a surface-enhanced Raman spectroscopy (SERS) taggant associated with a third barcode component; and wherein the barcode is formed by the first, the second, and the third barcode components.
The details of one or more implementations of the subject matter of this disclosure are set forth in the accompanying drawings and the subsequent description. Other features, aspects, and advantages of the subject matter will become apparent from the description, the drawings, and the claims.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.
Like reference numbers and designations in the various drawings indicate like elements.
This disclosure generally describes methods and systems for detecting tracers in a hydrocarbon reservoir. In some implementations, tracer studies can be used to collect data for the subsurface fluid flow analysis. In a tracer study, one or more tracers can be injected at an injection site of the reservoir. The tracer can mix with the fluid in the subsurface under the injection site. For example, the tracer can diffuse into the fluid or can mix with the fluid due to advection. After some time, fluid samples can be collected at a producing site for analysis. The propagation patterns of the tracers between the injecting site and the producing site can be used to determine the presence and location of flow barriers and fractures between the two sites in the reservoir. In some cases, multiple injection sites and multiple producing sites can be selected in a reservoir. Tracers can be injected in each of the multiple injection sites and fluid samples can be collected at each of the multiple producing sites to analyze the fluid pattern of the entire reservoir.
The effect of the tracer study can depend on the sampling frequency of the collection and the analysis of the fluid samples at the second location. In some cases, time-consuming processes, including for example, collection, purification, and concentration, may be performed prior to laboratory tracer analysis. In these or other cases, the fluid samples can be collected manually and brought back to a lab to perform these time-consuming processes. The sampling is therefore infrequent, for example, once a week. Due to the long timescales between sampling, the duration of tracer breakthrough may not be detected accurately. This can be a source of uncertainty during quantitative analysis, and therefore leading to inaccurate calculations of swept volume, fluid allocation, reservoir heterogeneity, and other reservoir management parameters.
In some implementations, a multi-modal tracer that is loaded with multiple taggants can be injected into the subsurface of a reservoir. Each of the multiple taggants can be associated with a different detection technique. Examples of the detection techniques include fluorescence (FL) spectroscopy, mass spectrometry (MS), surface-enhanced Raman scattering (SERS), or any other tracer detection techniques. Fluid samples can be extracted and the multi-modal tracer can be detected in real-time using a multi-modal detection device located at the producing site.
A wellbore drilling system, for example, the first wellbore drilling system 102 and the second wellbore drilling system 110, can be implemented to inject fluids into a subsurface of a reservoir, extract fluids from the subsurface of the reservoir, or a combination thereof. For example, the first wellbore drilling system 102 can inject fluid into the subsurface using a wellbore at an injection site. The second wellbore drilling system 110 can extract subsurface fluid using a wellbore at a producing site.
The multi-modal tracer 122 is a tracer that is loaded with more than one taggants. Each of the more than one taggants is associated with a specific detection methodology.
In the illustrated example, each of the multi-modal tracers 210 and 220 is loaded with three taggants: a FL taggant, a MS taggant, and a SERS taggant. Each taggant is associated with a different modality and can be detected using the respective detection methodology for that modality. A specific detection signal can be generated when a corresponding detection methodology is used to detect a multi-modal tracer. For example, when a FL detection is performed on the multi-modal tracer 210, a FL signal 212 can be generated. When a MS detection or a SERS detection is performed on the multi-modal tracer 210, a MS signal 214 or a SERS signal 216 can be generated. Each of the FL signal 212, the MS signal 214, and the SERS signal 216 represent a different component of a barcode for the multi-modal tracer 210. Similarly, each of a FL signal 222, a MS signal 224, and a SERS signal 226 represent a different component of a barcode for the multi-modal tracer 220.
As illustrated, the taggant associated with at least one modality of the multi-modal tracer 210 is different than the corresponding taggant associated with the same modality of the multi-modal tracer 220. Therefore, at least one bar code component of the multi-modal tracer 210 and the multi-modal tracer 220 are different. The mutli-modal tracers 210 and 220 can be differentiated based on the components of their barcodes. Using a linear combination of different taggants associated with each of the modalities, a library of barcodes can be generated. For example, if five different taggants are selected each for the FL, MS, and SERS modality, then 125 barcodes can be generated. Consequently, up to 125 different types of multi-modal particles can be used as tracers. Additional types of multi-modal particles can be available as the number of individual taggants increases. Using a multi-modal particle can significantly increase the number of unique tracers deployed in a tracer study of a reservoir.
In some implementations, the multi-modal particles can be implemented using nanoparticles. Alternatively, or in combination, the multi-modal particles can also be implemented using polymeric materials or inorganic compounds. For example, polymers containing monomeric units with functionalities that can be interrogated via different spectroscopic techniques can be incorporated within the same polymer chain. Inorganic complexes of rare earth (metallic ion) compounds coupled to various ligands can also be used.
In some cases, different multi-modal tracers from different injection site can arrive at the same producing site. If the fluid samples are collected infrequently, different tracers from different injection sites may arrive at the same producing sites within the same sample collecting period. Therefore, these tracers may be mixed together in the fluid samples, and may generate signals that are overlapped with one another and therefore may not be differentiated using the corresponding detection technology.
In some implementations, tracers can be detected at the producing site in real-time. Therefore, fluid samples can be collected frequently, and the tracers can be detected using the multi-modal detection device 112 in real-time.
The difference in the time of arrival can be detected by the multi-modal detection device 112 that performs detections in real time.
In the illustrated example, the tracer 302 is loaded with the FL taggant F1, the MS taggant M1, and the SERS taggant S1. The tracer 304 is loaded with the FL taggant F1, the MS taggant M2, and the SERS taggant S5. The response curves 320, 322, 324, 326, and 328 show the simulated response curves of the detection signals generated by each of these taggants using corresponding detection technologies. As shown by the curves 322 and 326, the intensity of the SERS signal produced by S1 rises to peak level at ΔT1 and before it falls, while the intensity of the intensity of the SERS signal produced by S5 rises to peak level at ΔT2 and before it falls. Similarly, shown by the curves 324 and 328, the intensity of the MS signal produced by M1 rises to peak level at ΔT1 and before it falls, while the intensity of the intensity of the MS signal produced by M2 rises to peak level at ΔT2 and before it falls. The peak of the MS signal produced by M1 occurs at the same time as the peak of the SERS signal produced by S1, while peak of the MS signal produced by M2 occurs at the same time as the peak of the SERS signal produced by S5. Because the curves are generated at real-time and can represent the change of concentration levels for each type of tracers over time, the response curves generated by the tracers 302 and 304 can be differentiated.
Returning to
In addition to generating a large barcode library through incorporation of many taggants into a single tracer, using multi-modal tracers in a tracer study can also take advantage of different benefits provided by each detection technique. For example, FL detection is a fast detection technique that can be used for interrogation at low concentration levels. However, the photophysical properties of most organic and inorganic compounds may prevent the generation of a large library of tracer materials due to the diffuse nature of electronic transitions. MS detection, on the other hand, can provide atomic mass resolution of taggants and thereby enabling the identification of tens to hundreds of different taggants simultaneously. The downside to MS detection is that fluids may require some level of automated pretreatment prior to analysis. The multi-modal detection device 112 can combine these two detection strategies. FL detection can be performed in-flow to indicate the arrival of tracers. In response to the indication, the sampling of fluid can be initiated and the MS, the SERS, or a combination thereof, can be performed in response. This approach can provide both fast and high-resolution detection of tracers. This approach can also provide multiple confirmations that a tracer is present, which can be beneficial under the harsh downhole conditions of the reservoir.
In operation, at the injecting site, one or more multi-modal tracers 122 can be mixed with the drilling fluid and injected into the subsurface by the first wellbore drilling system 102. The one or more multi-modal tracers 122 can mix with the subsurface fluid 120. Examples of the subsurface fluid 120 can include hydrocarbon products such as natural gas or petroleum, connate water, seawater, or any combinations thereof. At the producing site, the second wellbore drilling system 110 can extract the subsurface fluid 120. Fluid samples from the extracted subsurface fluid 120 can be analyzed using the multi-modal detection device 112 at the producing site. The multi-modal detection device 112 can detect the presence of the one or more multi-modal tracers 122.
At 402, a multi-modal tracer is injected at a first location in a reservoir. The multi-modal tracer mixes with the subsurface fluid in the reservoir. The multi-modal tracer includes a particle loaded with more than one taggants, each of the more than one taggants is associated with a different detection technology. At 404, fluid samples are collected at a second location in the reservoir. At 406, the fluid samples are analyzed to detect a presence of the multi-modal tracer in the fluid samples. In one example, at 412, a FL detection is performed to generate a first barcode component representing an FL signal associated with the FL taggant loaded on the multi-modal tracer, at 414, a MS detection is performed to generate a second barcode component, representing an MS signal associated with the MS taggant loaded on the multi-modal tracer. In some cases, additional detections can be performed to generate additional barcode components. At 416, a barcode is generated based on the first and the second barcode components. In some cases, the barcode can be generated further based on additional barcode components. At 418, the generated barcode is compared with multiple barcodes to detect the presence of the multi-modal tracer, where each of the multiple of barcodes is representing a particular multi-modal tracer. At 420, a subsurface fluid-flow pattern can be determined based on the detected presence of the multi-modal tracer.
For reservoir tracing applications, traditional fluorescence spectroscopy may have one or more issues. One issue is the presence of fluorescent materials within the oil matrix itself, providing a strong background signal. The schematic diagram 500 illustrates a two-dimensional fluorescence spectrum of Arabian-light crude oil. The horizontal axis represents the emission wavelengths. The vertical axis represents the excitation wavelengths. The two diagonal lines are an artifact of the measurement technique. As illustrated, the crude oil fluorescence dominates the visible portion of the spectrum (350-600 nanometers), which may impact the detection of tracers mixed with the crude oil. To mitigate this issue, complex separations and purifications may be performed to remove the background signal before the detection process of the tracers. This approach may be costly and time-consuming.
In some cases, upconversion or time-gated fluorescence spectroscopy can be used to improve the FL detection process. In an upconversion photophysical process, a material may emit photons of a higher energy than those that were absorbed. This anti-Stokes process may occur by two mechanisms: two-photon excitation or through long-lived metastable excited states. In a two-photon excitation process, a material can be excited with coherent high-power density lasers to enable near simultaneous adsorption of two-photons. The resulting excited state relaxes through emission of a photon with an energy roughly two times that of the exciting photons. Most molecules are capable of excitation through this mechanism. However, the quantum yields may be low so powerful excitation sources may be used. In a long-lived metastable excitation process, rare earth ion doped nanocrystals, that can be excited with low power sources such as continuous wave (CW) lasers or halogen lamps, can be used. Mechanistically, the rare earth ions are capable of achieving long-lived metastable excited states that allow multiple photons to be absorbed prior to an emission event, thus giving rise to an anti-Stokes type emission.
The upconversion luminescence can be used in the multi-modal detection process discussed previously. Upconverting taggants may be included as one element in a multi-component material that forms the multi-modal tracer. The tracers can undergo excitation at a wavelength that does not trigger fluorescence from the oil, thereby providing a clean observation of tracer luminescence in the presence of crude oil and reducing or avoiding additional separation procedures.
Alternatively, or in combination, time-gated fluorescence spectroscopy can be used to separate the luminescence of the tracer from the background fluorescence of the crude oil. In time-gated fluorescence spectroscopy, materials capable of emitting photons, on a time-scale longer than that of crude oil, can be used. The majority of chromophores in crude oil emit photons on a time scale of nanoseconds after excitation. Materials including sheathed lanthanide emitters and persistent phosphors can emit on a timescale of microseconds to hours, allowing for sample excitation with a pulsed flash lamp. This approach, followed by gating of the detection window, enables singular and unconvoluted sample observation after the crude oil has stopped emitting. This technique can achieve low detection limits in otherwise confounding media.
Persistent phosphor materials include inorganic complexes whose luminescence persists on a longer timescale, for example, seconds to hours.
These complexes offer a variety of advantages over traditional fluorophores for tracing applications. The emission from these materials can be very narrow, allowing for multiple barcodes without significant spectral overlap. The timescale of sheathed lanthanide emission ranges from microseconds to milliseconds, allowing for interrogation in fluids with high background signal. Rare earth ions can be mixed and matched with various ligands to create a large library of fluorescent taggants for multimodal composite tracers.
Raman spectroscopy uses inelastic scattering due to the interaction between incident monochromatic light and molecular vibrations. This process gives rise to scattered photons with energies that do not match the energy of the light source. When molecules are placed on or near a roughened metal surface or metal nanostructure such as gold, silver, and copper, Raman signal can be significantly enhanced by an order of 108-1015. Advancements in the controlled synthesis of nanostructures have further broadened the horizon of SERS phenomena to achieve single molecule sensitivities. SERS can be used as one of the detection technologies in the multi-modal detection process described previously because SERS provides ultra-low detection limits and has the resolution to uniquely identify different molecules.
In the multi-modal detection process, SERS active mode materials can be developed as modules for multi-modal tracers. The SERS module can include nanostructured cores and satellites, specific dye molecules (or organic molecules) and shells.
Thermally stable dye molecules embedded within nanoparticles can be detected by Raman spectroscopic techniques and yield enhanced detectability due to SERS phenomena. Many dye molecules have this characteristic, and therefore a large number of SERS taggants can be used to form the multi-modal tracer.
Mass spectrometry (MS) can be used to identify and quantify chemicals (both molecular and atomic) based on their mass to charge ratio. The analysis can be performed in two steps: (1) the analyte is ionized and (2) the mass to charge ratio is defined by the motion of the charged particles in an applied electromagnetic field. Mass spectrometry can achieve atomic mass resolution and the limits of detection can be lower than the ppt level.
The integration of mass taggants into a multi-modal composite tracer can be achieved in a variety of ways and length scales. At the smallest length scale, a fluorescent molecule or complex exhibiting SERS activity can also be identified using mass spectrometry. Moving from the molecular to macromolecular scale, polymeric species composed of specific monomers, combinations of monomers, or side chains can be analyzed after triggered degradation. The same technique applies to nanoarchitectures, as well.
The MS taggants themselves can include organic species, inorganic ions, or a combination thereof. Mixing multiple MS taggants into a single multi-modal composite material can increase the number of possible barcodes. In the polymeric and nano-based tracer materials, triggered degradation can occur via multiple mechanisms. For example, organic polymeric materials can be depolymerized via hot filament ionization where the temperature of the filament exceeds the ceiling temperature of the polymer. Inorganic nanomaterials can be degraded through the use of inductively coupled plasma (ICP) or dissolution in an acidic medium. MS taggants can also be developed using programmed extraction capabilities. This can be implemented by doping polymeric nanomaterials with hydrophobic taggants that can be released from the nanomaterial via treatment with an appropriate solvent. Fluorinated MS taggants can provide highly targeted extraction using the concept of fluorous affinity.
This description is presented to enable any person skilled in the art to make and use the disclosed subject matter, and is provided in the context of one or more particular implementations. Various modifications to the disclosed implementations will be readily apparent to those skilled in the art, and the general principles defined herein may be applied to other implementations and applications without departing from scope of the disclosure. Thus, the present disclosure is not intended to be limited to the described and/or illustrated implementations, but is to be accorded the widest scope consistent with the principles and features disclosed herein.
Accordingly, the previous description of example implementations does not define or constrain this disclosure. Other changes, substitutions, and alterations are also possible without departing from the spirit and scope of this disclosure.
This application claims the benefit of priority of U.S. Provisional Application Ser. No. 62/434,804, filed on Dec. 15, 2016, which is incorporated by reference herein in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62434804 | Dec 2016 | US |
