SYSTEM AND METHOD FOR SUBSAMPLING A GASEOUS SUBSAMPLE FROM A MONOPHASIC FLUID FOR NOBLE GAS ANALYSIS

Abstract

The invention relates to a subsampling system or method of a monophasic fluid (2) for the preparation of a gaseous subsample (2b). said subsampling system (1) comprising: a first inlet valve (11). an expandable cell (20). a second valve (41), and an expansion cell (40); said first inlet valve (11) being arranged so as to control the flow of the monophasic fluid to the expandable cell (20); said expandable cell (20) being arranged to allow the expansion of the monophasic fluid (2) until forming a diphasic fluid (2a) at a known pressure. volume and temperature. said diphasic fluid (2a) comprising a gas phase and a liquid phase: said second valve (41) being arranged so as to control the flow of the gas phase to the expansion cell (40); and said expansion cell (40) being arranged so as to contain the gaseous subsample (2b) of the monophasic fluid (2).

Claims

1. A subsampling system of a monophasic fluid for the preparation of a gaseous subsample, said subsampling system comprising: a first inlet valve, an expandable cell, a second valve, and an expansion cell; said first inlet valve being arranged so as to receive the monophasic fluid, and to control a flow of the monophasic fluid to the expandable cell; said expandable cell being thermoregulated, equipped with a pressure gauge and arranged to allow the expansion of the monophasic fluid until forming a diphasic fluid at a known pressure, volume and temperature, said diphasic fluid comprising a gas phase and a liquid phase; said second valve being arranged so as to control a flow of the gas phase to the expansion cell; said expansion cell being arranged so as to receive at least a part of the gas phase, said at least a part of the gas phase forming the gaseous subsample of the monophasic fluid; and the subsampling system being arranged to allow a measurement of a temperature inside the expandable cell.

2. The subsampling system according to claim 1, wherein it is arranged to allow a measurement of a pressure inside the expandable cell and to control an inner volume and temperature of the expandable cell.

3. The subsampling system according to claim 1, further comprising a temperature controller, an electronic pressure monitor, and a volume controller, respectively configured to determine a temperature value, a pressure value and a volume value of the expandable cell when a bubble point occurs.

4. The subsampling system according to claim 1, wherein the whole subsampling system is thermoregulated.

5. The subsampling system according to claim 1, further comprising a three-way valve and a draining point, said three-way valve being connected to the draining point and positioned right before and/or right after the expandable cell.

6. The subsampling system according to claim 1, further comprising a low-pressure section arranged to allow a gas pressure to reach a target pressure selected from 1 to 10 bars.

7. The subsampling system according to claim 1, further comprising at least one subsampling cells removably fixed to the subsampling system and arranged so as to collect at least a part of the gaseous subsample at a pressure between 1 bar and 10 bars.

8. The subsampling system according to claim 6, wherein the low-pressure section comprises at least one subsampling cells removably fixed to the subsampling system and arranged so as to collect at least a part of the gaseous subsample at a pressure between 1 and 10 bars.

9. The subsampling system according to claim 3, wherein the temperature controller is configured to maintain a temperature of 40 C. to 60 C. in the expandable cell.

10. The subsampling system according to claim 3, wherein the volume controller is further configured to increase or decrease a volume of the expandable cell.

11. The subsampling system according to claim 1, wherein the expandable cell is equipped with a movable inner surface, said movable inner surface being arranged to increase or decrease a volume of the expandable cell.

12. The subsampling system according to claim 1, further comprising an observation cell positioned between the expandable cell and the expansion cell.

13. A method of subsampling a monophasic fluid, for the preparation of a gaseous subsample using a subsampling system comprising a first inlet valve, an expandable cell, a second valve, and an expansion cell, the subsampling system being arranged to allow a measurement of a temperature inside the expandable cell; said subsampling method comprising: Connecting a monophasic fluid source to the subsampling system so that the first inlet valve of said subsampling system receives the monophasic fluid and controls monophasic fluid flow to the expandable cell; Operating the first inlet valve so that the expandable cell receives, through the first inlet valve, at least a fraction of the monophasic fluid; Expanding the expandable cell, at a known pressure, volume and temperature, until the monophasic fluid is transformed into a diphasic fluid, said diphasic fluid comprising a gas phase and a liquid phase; Operating the second valve, said second valve controlling a gas phase flow to the expansion cell, so as to transfer only the gas phase from the expandable cell to the expansion cell; and Sampling at least a part of the gas phase comprised in the expansion cell to obtain the gaseous subsample.

14. A subsampling method according to claim 13, wherein the gaseous subsample is brought to a pressure of less than 10 bars.

15. A subsampling method according to claim 13, wherein the subsampling system further includes a way, through a draining point, to remove the liquid part, pump only the expandable cell and recharge it with the monophasic fluid in order to cumulate gas in the expansion cell.

16. A subsampling method according to claim 13, wherein the subsampling system comprises an observation cell, and the subsampling method also comprises a step of operating the second valve until a liquid is observed through the observation cell so as to transfer only the gas phase from the expandable cell to the expansion cell.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0054] The foregoing and other objects, features and advantages of the present invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings in which:

[0055] FIG. 1 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid according to the invention.

[0056] FIG. 2 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid according to the invention.

[0057] FIG. 3 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a draining point and an observation cell, according to the invention.

[0058] FIG. 4 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a draining point and an observation cell, according to the invention.

[0059] FIG. 5 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a low-pressure section, according to the invention.

[0060] FIG. 6 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a draining point, an observation cell and a low-pressure section, according to the invention.

[0061] FIG. 7 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a draining point, an observation cell and a low-pressure section, according to the invention.

[0062] FIG. 8 is a schematic view showing an embodiment of a subsampling system of a monophasic fluid, comprising a draining point, an observation cell, a three-way-vale, and a low-pressure section, according to the invention.

[0063] FIG. 9 is a schematic view showing a subsampling method of a monophasic fluid, for the preparation of a gaseous subsample according to an embodiment of the invention. Facultative steps are represented in dotted frames.

DETAILED DESCRIPTION

[0064] A description of example embodiments of the invention follows.

[0065] In the following description, Subsampling means or implies a procedure by which a smaller, representative sample is taken from a larger sample.

[0066] In the following description, a monophasic fluid corresponds to a particular state of a fluid having one phase which is liquid form or gas form, or supercritical form. Preferably, a monophasic fluid corresponds to a state of a fluid having one phase which is liquid form.

[0067] In the following description, gaseous subsample is about collecting a fraction of a sample in a gas form

[0068] In the following description, low-pressure section means a section of a subsampling system configured to an operating pressure of less than 20 bar.

[0069] In the following description, high-pressure means a pressure higher than 20 bar, a high-pressure section means a section of a subsampling system configured to an operating pressure of more than 20 bar.

[0070] In the following description, noble gases refers to a series of chemically inert elements that exhibit similar properties. The noble gases are a group of chemically inert, or conservative, gases which have a low natural abundance in natural fluids. Various physical processes have resulted in different pools of noble gases (the mantle, atmospheric and crustal pools) becoming distinct in their isotopic composition and relative elemental abundances. The five noble gases of particular interest in the present invention are helium (He), neon (Ne), argon (Ar), krypton (Kr) and xenon (Xe).

[0071] By process, compute, determine, display, extract, compare or more broadly executable operation is meant, within the meaning of the invention, an action performed by a computer device or a processor unless the context indicates otherwise. In this regard, the operations relate to actions and/or processes of a data processing system, for example a computer system or an electronic computing device, which manipulates and transforms the data represented as physical (electronic) quantities in the memories of the computer system or other devices for storing, transmitting or displaying information. In particular, calculation operations are carried out by the processor of the device, the produced data are entered in a corresponding field in a data memory and this field or these fields can be returned to a user for example through a Human-Machine Interface formatting such data. These operations may be based on applications or software.

[0072] The terms or expressions application, software, program code, and executable code mean any expression, code or notation, of a set of instructions intended to cause a data processing to perform a particular function directly or indirectly (for example after a conversion operation into another code). Exemplary program codes may include, but are not limited to, a subprogram, a function, an executable application, a source code, an object code, a library and/or any other sequence of instructions designed for being performed on a computer system.

[0073] By processor is meant, within the meaning of the invention, at least one hardware circuit configured to perform operations according to instructions contained in a code. The hardware circuit may be an integrated circuit. Examples of a processor include, but are not limited to, a central processing unit, a graphics processor, an application-specific integrated circuit (ASIC according to Anglo-Saxon terminology), and a programmable logic circuit. A single processor or several other units may be used to implement the invention.

[0074] By coupled is meant, within the meaning of the invention, connected, directly or indirectly, with one or more intermediate elements. Two elements may be coupled mechanically, electrically or linked by a communication channel.

[0075] The expression human-machine interface, within the meaning of the invention, corresponds to any element allowing a human being to communicate with a computer, in particular and without that list being exhaustive, a keyboard and means allowing in response to the commands entered on the keyboard to perform displays and optionally to select with the mouse or a touchpad items displayed on the screen. Another embodiment is a touch screen for selecting directly on the screen the elements touched by the finger or an object and optionally with the possibility of displaying a virtual keyboard.

[0076] By computer device, it should be understood any device comprising a processing unit or a processor, for example in the form of a microcontroller cooperating with a data memory, possibly a program memory, said memories possibly being dissociated. The processing unit cooperates with said memories by means of internal communication bus.

[0077] When introducing elements of various embodiments of the present disclosure, the articles a, an, and the are intended to mean that there are one or more of the elements. The terms comprising, including, and having are intended to be inclusive and mean that there may be additional elements other than the listed elements.

[0078] Additionally, it should be understood that references to one embodiment or an embodiment of the present disclosure are not intended to be interpreted as excluding the existence of additional embodiments that also incorporate the recited features.

[0079] Chemical elements can partition differently between phases. Hence the analysis of a monophasic fluid sampled in extreme environment (i.e., pressure more than 20 bar or temperature >100 C.) can be biased when the subsampling is not correctly done. To calculate the concentration of chemical elements, such as noble gas, in each phase at the time of sampling, several approximations are usually done, this leading to inaccurate results.

[0080] In particular, PVT sampling bottles, containing a complex fluid, are used through a pressure decrease to create gaseous samples. However, such a generation of gaseous samples, when it is done without any parameter control, lead to a degradation of the content of the sampling bottle and show a low reproduction rate.

[0081] The inventors developed a new solution for isolating chemical elements, in particular noble gases, from complex fluids such as fluids containing water-gas-oil mixtures. The solution can be described as an offline extraction system configured to isolate a gaseous subsample from a high-pressure monophasic fluid.

[0082] The invention thus relates to a method or system for obtaining a representative noble gas sample from a monophasic sample, where the precise pressure, volume and temperature conditions are known or controlled, allowing for the calculation of the original noble gas composition in a monophasic fluid.

[0083] The detailed description focuses only on the description of a pressurized liquid subsampling for noble gas analysis. However, this invention can be applied to other monophasic fluids requiring a phase split under controlled conditions to be able to recombine the initial chemical (e.g., noble gas) content of the initial liquid fluid.

[0084] According to a first aspect, the invention relates to a subsampling system 1 of a monophasic fluid 2.

[0085] Such a subsampling system 1 is particularly relevant for the preparation of a gaseous subsample 2b from the monophasic fluid 2, said gaseous subsample being adapted to noble gas analysis.

[0086] As shown in FIG. 1, the subsampling system 1 comprises a first inlet valve 11, an expandable cell 20, a second valve 41, and an expansion cell 40.

[0087] As it will be described hereafter, this subsampling system 1 can be used under various arrangements.

[0088] Essentially, this subsampling system 1 will comprise two main parts: a phase split part and a low-pressure part.

[0089] The split part will in particular comprise the first inlet valve 11 and the expandable cell 20. This split part is configured to induce a phase split in the monophasic fluid 2 under highly controlled conditions. Indeed, the phase split is preferably monitored through temperature, volume, and pressure measurements.

[0090] The low-pressure part will in particular comprise the expansion cell 40. This low-pressure part is configured to induce an expansion of the gaseous subsample and thus to reduce the pressure of this gaseous subsample under controlled conditions (e.g., a defined volume of the expansion cell 40).

[0091] Each element of the subsampling system 1 will be described in detail and some the preferred embodiments will be illustrated.

[0092] First inlet valve 11

[0093] The first inlet valve 11 is preferably arranged so as to receive the monophasic fluid 2. For example, the monophasic fluid 2 can be received through the first inlet valve 11 from a sampling bottle 10. In particular, the first inlet valve 11 is adapted to be connected to a PVT

[0094] (Pressure, Volume, Temperature) sampling bottle.

[0095] Indeed, the invention relates to the subsampling of a gaseous phase of a monophasic fluid 2 sampled in an extreme environment such as a high-pressure environment. In order to keep the distribution of species unperturbed, the monophasic fluid 2 is preferably maintained in a controlled environment reflecting the initial sampling conditions.

[0096] The first inlet valve 11 is preferably configured to control the flow of the monophasic fluid 2 from the sampling bottle 10 to the expandable cell 20.

[0097] Advantageously, the first inlet valve 11 is arranged to take a very low volume sample from the monophasic fluid source. Preferably, the system is arranged so that the first inlet valve 11 is capable of transferring an aliquot of less than 10 cc from the monophasic fluid source, preferably less than 5 cc, more preferably less than 1 cc.

[0098] The first inlet valve 11 can be a two-way or a three-way inlet valve. It can be selected from automated or manual valves. For example, the use of pneumatically actuated inlet valves enables full automation of subsample preparation and eventually post-analysis clean up.

[0099] Preferably, the first inlet valve 11 has to be designed to support a pressure ranging from 10 7 mbar to 1000 bars.

[0100] Expandable cell 20

[0101] As illustrated in the FIG. 1, the subsampling system 1 according to the invention also comprises an expandable cell 20.

[0102] Advantageously, the expandable cell 20 is thermoregulated and the pressure in the expandable cell 20 is monitored.

[0103] Moreover, the expandable cell 20 has the particularity to be arranged to allow a controlled and variable expansion of the monophasic fluid 2.

[0104] The controlled and variable expansion of this expandable cell 20, in particular of its inner volume, can be managed through various ways, for example using a movable inner surface like a movable piston or a movable wall such as in a syringe cell. For example, a movable inner surface that can be moved through the use of a fluid controlled by one or several valves. For example, the expandable cell can be composed of different chambers separated with valves and the expansion is controlled by the connection of the initial volume to additional volumes of supplementary chambers.

[0105] In particular, the expandable cell 20 can be equipped with at least one movable surface such as a piston 23, preferably said piston 23 being arranged to increase or decrease the volume of the expandable cell 20.

[0106] The expandable cell 20 will be preferably calibrated. The calibration will ensure that the precise inner volume of the expandable cell 20 will be known in a range of at least 5 cc, preferably 30 cc, more preferably 200 cc. For example, the inner volume of the expandable cell 20 can be known continuously from a 1 cc volume to a 200 cc volume.

[0107] Moreover, the system can comprise a volume controller 24. The volume controller may be an electronic volume controller configured to control the increasing or decreasing of the volume of the expandable cell 20. Such control can be carried out through a human-machine interface. Alternatively, the system can comprise a manual volume controller 24 configured to control the increasing or decreasing of the volume of the expandable cell 20.

[0108] Such an expansion is preferably possible until the monophasic fluid 2 forms a diphasic fluid 2a. The said diphasic fluid 2a comprising a gas phase and a liquid phase.

[0109] Hence, as it has already been discussed, the subsampling system 1 according to the invention is configured to make an expansion of the monophasic fluid 2 at a controlled: [0110] volume, [0111] pressure and [0112] temperature.

[0113] The volume of the expandable cell 20 can be measured based on the displacement value(s) of movable(s) part(s) of the expandable cell 20. In particular, volume measurement means can be connected to electronic volume monitor configured to determine the volume value of the expandable cell 20 when the bubble point occurs.

[0114] The pressure in the expandable cell 20 can be monitored for example through the pressure gauge 22 or any other means adapted for pressure measurement in the expandable cell 20. For example, a baratron@ manometer can be fitted in a part of the expandable cell 20 and is preferably capable of measuring from 20 mTorr to 10000 Torr. In particular, pressure measurement means can be connected to electronic pressure monitor configured to determine the pressure value of the expandable cell 20 when the bubble point occurs.

[0115] The temperature in the expandable cell 20 can be monitored for example through the temperature sensor or temperature gauge or any other means adapted for temperature measurement in the expandable cell 20. In particular, the temperature in the expandable cell 20 can be monitored directly (e.g. in the expandable cell) or indirectly (e.g. through an external temperature measurement) by the measurement means. For example, the expandable cell can be put in a closed volume with a controlled temperature (e.g. an oven). For example, the expandable temperature can be surrounded by a heating mat or heating cable.

[0116] In particular, temperature measurement means can be connected to an electronic temperature controller 70 configured to determine the temperature value of the expandable cell 20 when the bubble point occurs. Moreover, the system can comprise a temperature controller configured to monitor and control the sample temperature in the expandable cell 20.

[0117] Preferably, the subsampling system 1 according to the invention comprises an expandable cell 20 which is arranged to allow the expansion of the monophasic fluid 2 to form, at a bubble point, a diphasic fluid, and wherein the temperature controller 70, preferably the electronic temperature controller, the electronic pressure monitor, and the volume controller 24, preferably electronic volume controller, are configured to determine the temperature value, the pressure value and the volume value of the expandable cell 20 when the bubble point occurs.

[0118] System according to the invention can also comprise controllers configured to identify the instant when the bubble point occurs.

[0119] Such an expandable cell 20 can preferably be a high-pressure expandable cell. Indeed, this expandable cell should be configured to sustain pressure of more than 100 bar, and up to 1000 bars. For example, the expandable cell 20 can be a high-pressure syringe. As illustrated in FIG. 1, a system according to the invention also comprises an expansion cell 40 and a second valve 41.

[0120] The second valve 41 being arranged so as to control the flow of the gas phase to the expansion cell 40.

[0121] As mentioned, the expansion cell 40 is part of a low-pressure part configured to induce an expansion of the gaseous subsample.

[0122] The expansion cell 40 is preferably arranged so as to contain at least a fraction of the gas phase formed from the monophasic fluid 2, named the gaseous subsample 2b of the monophasic fluid 2.

[0123] The low-pressure part will in particular comprise the expansion cell 40. This low-pressure part is configured to induce an expansion of the gaseous subsample and thus reducing the pressure of this gaseous subsample under controlled conditions (e.g., a defined volume of the expansion cell 40).

[0124] The expansion cell 40 is preferably a high-pressure expansion cell 40. For example, this expansion cell 40 should be configured to sustain pressure between 10-7 mbar and 1000 bar.

[0125] As shown in FIG. 2, the subsampling system 1 can be thermoregulated. In particular, the system can comprise a temperature controller 70, preferably electronic, for temperature control of the expandable cell 20, preferably said electronic temperature controller 70 is configured to maintain a temperature of 40 C. to 60 C. in the expandable cell 20.

[0126] As illustrated in FIGS. 2, 3 and 4 a system according to the invention can comprise a draining point 30.

[0127] This draining point 30 can be used to discard part of the monophasic fluid 2 or of the liquid phase after its entry in the expandable cell 20 or the expansion cell 40.

[0128] This draining point 30 can be coupled with at least one three-way valve 21, said at least one three-way valve 21 being connected to the draining point and positioned right after (FIG. 2) and/or right before (FIG. 3) the expandable cell 20.

[0129] The system can also comprise an observation cell 31. Such an observation cell 31 can be positioned between the expandable cell 20 and the high-pressure expansion cell 40. It can be for example positioned after (FIG. 2) or before (FIG. 4) the draining points, but it has to be separated from the expandable cell with a valve.

[0130] The observation cell 31 is preferably a sapphire cell but it can also be selected from: borosilicate window or diamond cell.

[0131] The system can also comprise several pressure gauges such as thermal conductivity gauge, Pirani gauge, Penning gauge or ion gauge which are fitted onto the line for monitoring the pressure in vacuum systems.

[0132] The system can also comprise several valves. For example, the subsampling system 1 can comprise a further a three-way valve 21, said three-way valve being positioned between the second valve 41 and the high-pressure expansion cell 40.

[0133] As illustrated in FIGS. 5, 6, 7 and 8, a subsampling system according to the invention can comprise a low-pressure section 3. Such low-pressure section 3 can for example be arranged to allow the gas pressure to reach a target pressure, preferably said target pressure being selected from 1 to 10 bars.

[0134] The system according to the invention, and in particular the low-pressure section, comprises subsampling cells 50, 60. The low-pressure section can also comprise a dedicated pressure gauge 43.

[0135] In particular, the system 1 according to the invention can comprise at least one, preferably two, subsampling cells 50, 60 arranged so as to collect at least part of the gaseous subsample at a pressure comprised between 1 bar and 10 bars.

[0136] The subsampling cells 50, 60 can also be removably fixed to the subsampling system 1. Hence the subsampling cells 50, 60 are arranged so as to be dissociated from subsampling system 1 and to be transportable.

[0137] Hence, the system according to the invention can be installed at the site of sampling of the monophasic fluid 2 and the subsampling cells are transported as such to extraction/purification line connected to a spectrometer. Alternatively, the system according to the invention can be installed in a laboratory and the system can be automated to directly inject the subsample in the extraction/purification line connected to a spectrometer.

[0138] Optionally the system 1 can comprise a reservoir tank which allows subsample aliquots to be easily stored into the system. The previously prepared gases stored in the tank can be used for analyses by automated operation in the system. Therefore, those stored gases make it possible to run overnight measurements automatically.

[0139] Optionally, the purification line can comprise purification means such as Ti-sponge furnace or Getter pump or cadmium acetate microporous media or silver wool porous media or zeolites or SAES GP 50 or active charcoal. Such purification means can be of particular interest when the monophasic fluid can comprise H.sub.2S to be removed before storage. It should be understood that analytical means for noble gas analysis such as mass-spectrometer can also comprise purification line.

[0140] The system may also comprise at least one turbo pump 90 configured to allow subsampling under high vacuum conditions.

[0141] In another aspect, the invention relates to a subsampling method 100 of a monophasic fluid 2.

[0142] Such a method allows obtaining a gaseous subsample 2b from a monophasic sample, preferably a liquid sample.

[0143] A method according to the invention can use a system 1 according to the invention. However, it can also use any system comprising a first inlet valve 11, an expandable cell 20, a second valve 41, and an expansion cell 40. In particular, the system used by a method according to the invention can comprise an expandable cell 20 being connected though a three-way valve 21 to an expansion cell 40 and a draining point 30, the first inlet valve 11 being arranged so as to receive the monophasic fluid 2 from a sampling bottle 10; and said expandable cell 20 being thermoregulated and equipped with a pressure gauge 22, said expansion cell 40 being arranged to receive the subsample for the noble gas analysis.

[0144] A method according to the invention will preferably comprise phase split step that will make the initial monophasic fluid 2 turn into a diphasic fluid under equilibrium and an expansion step that will allow the gas pressure of the gaseous subsample to reach the target pressure (e.g., 1-10 bars).

[0145] As illustrated in FIG. 9, the subsampling method 100 according to the invention, comprise the step of connecting 120 a monophasic fluid source to the subsampling system 1, Operating 130 the first inlet valve 11; Expanding 140 the expandable cell 20 to obtain a diphasic fluid; Transferring 150 at least a part of the gas phase from the expandable cell 20 to the high-pressure expansion cell 40; and Sampling 160 the gas phase comprised in the high-pressure expansion cell 40 to obtain the gaseous subsample 2b.

[0146] Moreover, a method according to the invention can comprise a step of preparing 110 the system to the subsampling, a step of reducing 170 the pressure of the gaseous subsample and a step of purifying 180 the gaseous subsample.

[0147] A first step can relate to preparing 110 the system to the subsampling. The method is particularly suited for noble gas sampling and the main source of noble gas is the air. Indeed, with the exception of helium the noble gases are many orders of magnitude lower in liquid samples than in air. Hence, the subsampling process must avoid any dead volume (not pumped) and reach a secondary vacuum (107-105 mbar under pumping).

[0148] Before subsampling, the system and in particular the low-pressure section should be pumped. During flushing, temperature and electrical conductivity should be checked to see if the values stabilize.

[0149] The method according to the invention is particularly advantageous for samples taken in from extreme environment such as downhole samples. The monophasic fluid 2 has preferably a pressure range from 100 to 1000 bars.

[0150] A step relates to connecting 120 a monophasic fluid source to the subsampling system 1. Such a connection is preferably made so that the first inlet valve 11 of said subsampling system 1 receives the monophasic fluid 2 and control monophasic fluid 2 flow to the expandable cell 20.

[0151] As described, the monophasic fluid source can be a bottle specifically dedicated to high-pressure collection or any other means adapted for monophasic sample collection from extreme conditions.

[0152] The method also comprises a step of operating 130 the first inlet valve 11 so that the expandable cell 20 receives, through the first inlet valve 11, at least a part of the monophasic fluid 2. Operating the first inlet valve 11 can be automatic or manual.

[0153] Advantageously, the transfer of the monophasic fluid 2 from the monophasic fluid source 10 to the expandable cell 20 is an isobar transfer. More preferably, transfer is done so as the pressure in the monophasic fluid source vary of less than 5 percent, preferably less than 1 percent.

[0154] Typically, the first inlet valve 11 will be open in order to transfer a small aliquot of the monophasic fluid 2 into the expandable cell 20. Preferably, the operating step will allow a transfer of the monophasic fluid 2 from the monophasic fluid source 10 to the expandable cell 20, said transfer corresponding for example to 1 cc. However, a higher volume of the monophasic fluid 2 can be transfer from the monophasic fluid source 10 to the expandable cell 20, such as more that 1cc, more than 2 cc or more than 5 cc.

[0155] Moreover, when the aliquot is taken, the monophasic fluid source, such as a PVT bottle, can be controlled in pressure and temperature.

[0156] The method also comprises a step of expanding 140 the expandable cell 20. In particular, it refers to the expansion of the inner volume of the expandable cell 20. The expansion is done preferably at a known pressure, volume and temperature.

[0157] With an increase of the internal volume of the expandable cell, the pressure of the monophasic fluid 2 is preferably decreased at a controlled rate until a bubble point is reached. At the instant of the bubble point, the monophasic fluid 2 is transformed into a diphasic fluid 2a, said diphasic fluid 2a comprising a gas phase and a liquid phase.

[0158] The method of the invention will preferably comprise a monitoring of how gas evolves from oil when pressure falls below the bubble point, this method is comparable to CCE (Constant Composition Expansion), also called CME (Constant Mass Expansion). This method is already known by the person of the art and is described for example in Danesh, A. (1998). PVT and phase behaviour of petroleum reservoir fluids, Elsevier.

[0159] Hence, the expansion of the expandable cell 20 is preferably done at a rate slower than 0.5 cc per minute.

[0160] Hence, the monophasic fluid 2 will be able to support another round of expansion in order to reach it bubble point.

[0161] As the sample of expanded monophasic fluid 2 is measured as well as the pressure and the volume of the expandable cell 20, a second or third expansion can be done without losing the benefits of the present invention.

[0162] Advantageously, while the fluid is expanded into the expandable cell 20 volume, the method according to the invention comprises the recording of pressure, temperature and volume values in order to perform a pressure-volume curve (PV curve).

[0163] The method also comprises a step of operating 150 the second valve 41.

[0164] Said second valve 41 controlling the gas phase flow to the expansion cell 40, so as to transfer only the gas phase from the expandable cell 20 to the expansion cell 40, preferably the high-pressure expansion cell 40.

[0165] Finally, the method comprises a sampling 160 of the gas phase comprised in the expansion cell 40 to obtain the gaseous subsample 2b. Preferably, a step of sampling at least a part of the gas phase.

[0166] The gaseous subsample 2b will be suitable for chemical analysis and in particular for a noble gas analysis.

[0167] The method according to the invention also preferably comprises a step of maintaining a constant temperature for the whole subsampling system. Such a maintained constant temperature is preferably over 40 C., more preferably over 50 C.

Example

[0168] A downhole sample collected at a pressure range from 100 to 1000 bars is selected as a monophasic sample. Subsampling of such a high-pressure sample is not an easy task.

[0169] However, if the samples were to be collected at the well head, the samples will be at low pressure (1-10 bar) and will be highly fractionated thought the temperature and pression variation from the downhole to the well head.

[0170] Hence, if one wants to decipher exact concentrations of chemical elements from extreme environment samples, it should subsample the monophasic fluid source in particular manners and in particular at pressure and temperature reflecting the extreme environment.

[0171] Regarding the FIG. 8, at the beginning of the process, the valves 11 should be closed, and valves 21, 42, 51, 52 and 61 opened, (Valve 21 is opened to connect volumes 20 to 40, but is closed to the draining point). A turbomolecular pumping system is connected to the valve 61 and the whole system is pumped under high vacuum. The expandable cell 20 is adjusted to its minimum volume. Once the whole system under high vacuum, the valve 21 is closed.

[0172] The valve 11 is open in order to transfer an aliquot of the monophasic fluid source to the expandable cell 20. In particular, a 1cc capillary can be maintained at reservoir pressure and reservoir temperature between the PVT bottle and the expandable cell 20. The 1cc capillary is filled with the monophasic fluid 2 and then isolated from the PVT bottle to avoid any risk of damaging the fluid integrity.

[0173] The expandable cell 20 volume is adjusted gradually to the bubble point of the monophasic fluid 2. In particular, the fluid is expanded into the syringe volume. At this stage, if the bubble point pressure is unknown, a PV curve is advantageously performed to characterize it. The syringe volume is increased to up to its maximum (e.g. 30cc). The pressure can be below the bubble point pressure meaning the fluid became diphasic.

[0174] If the expandable cell 20 is adjusted to its maximum volume and the bubble point did not occur, the pressure was not low enough to reach the bubble point.

[0175] The valves 11 and/or 21 can be opened while access to the monophasic fluid source is closed. The expandable cell 20 is retracted while the expanded monophasic fluid 2 is removed.

[0176] Once the expandable cell 20 has been retracted to its minimum volume, and the whole system is pumped until 10.sup.5 to 10.sup.6 mbar, the residual fluid is expended one more time into the syringe.

[0177] Finally, the expanded monophasic fluid 2 is introduced in the expandable cell 20 and the expandable 20 volume is adjusted gradually to the bubble point of the monophasic fluid 2.

[0178] Once the monophasic fluid 2 is transformed in a diphasic fluid, the valve 21 is open to the sapphire cell. The fluid phase is checked through the sapphire cell. Valve 41 is open and only gas was transferred to the expansion cell 40.

[0179] If any drop of liquid is observed through the sapphire cell, the valve 41 is closed.

[0180] Then the gas phase from the monophasic fluid 2 is allowed to expand the sample into the expansion cell. The valve 41 is closed to isolate the gas phase, then while the valve 51 is closed, the valve 42 is opened to have a lecture of the pressure into the expansion cell 40.

[0181] Depending on the pressure at this stage, different gas expansions are possible to target a final pressure in the noble gas cell between 2 and 4 bars.

[0182] Composition of the gas can then be measured for example on a noble gas mass spectrometer.

[0183] The composition of the noble gas in the monophasic fluid 2 is back calculated based on the bubble conditions of the fluid, for example based on a calculated PV curve.

[0184] As it has been discussed, the solution developed by the inventors allow, through a phase split under controlled conditions and an expansion phase, reaching a pressure compatible with spectrometer to identify the initial content of the initial monophasic fluid 2, in particular in noble gas.