This invention relates to devices used in oil and gas industry.
Gas chromatography is a well-known measurement method based on the introduction of a small amount of the test gas in the permanent flow of a known neutral gas (the carrier gas, or the transporting medium) following which the gases are passed through a capillary pipe. Due to the difference in the mobility of individual gases contained in the sample, the sample is separated in different portions each consisting of an individual gas. At the outlet of the capillary tube these gas portions can be identified using different methods. Thus, the complete chemical composition of the sample can be determined. Advantage of the chromatographic method is the possibility to considerably simplify the design of upstream detectors while retaining the high resolution of the whole system.
Gas chromatography is widely used in oil and gas industry for drilling mud sample analysis and allows to determine the concentrations of H2S, CH4, C2H6 etc. in gases mixed with the output drilling mud flow. The carrier gas is usually helium or nitrogen.
For the implementation of this method, the equipment used for sampling and formation fluid borehole analysis can be lowered into the well using cable or drilling pipe. The tools are installed on borehole wall, following which a water seal is produced on the wall. Then a sonde is installed in the being tested formation to provide a hydraulic connection with the latter. Formation fluid samples in amounts from several cubic centimeters to hundreds of liters are extracted from the formation by the tool for transferring to the surface and/or in-situ analysis. In some cases the samples are drained back into the well after the completion of in-situ analysis. Fluid analysis methods comprise measurement of fluid specific resistivity, fluid color or light absorption, density (as a function of γ-radiation absorption), gas concentration (by refraction/reflection of gas bubbles in thin pipes) etc. Besides, fluid parameter special measurements are performed: pressure and temperature exact values for different flow modes are recorded using the detectors.
The development of a device allowing borehole analysis methods to be implemented using a gas chromatograph is of special interest. So far, no counterparts of this technical solution have been considered, because chromatographic pipes are very long, and a single analysis session including sample separation into the components of interest requires much time. Moreover, a large amount of gas is taken for a sample. Therefore disadvantage of the existing borehole chromatograph design is its large dimensions and weight making it unsuitable and complex when used in different practical field conditions.
Gas chromatography, especially gas-liquid chromatography, deals with samples that are preliminarily transferred to the vapor phase and supplied to the head of the chromatographic column (
For optimum chromatograph operation, the sample should not be very large and should be introduced into the column in the form of a ‘vapor plug’: slow introduction of large samples brings to washing-out the boundaries and to resolution impairment. The most common sample introduction method is those using a microsyringe for sample introduction through a rubber seal into the fast evaporator channel in the column head. The sample channel temperature is usually 50° C. above the boiling point of the least volatile sample component. For packed columns, the sample size ranges within tenths of microliter to 20 microliters. For capillary columns, noticeably smaller samples are required, usually about 10−3 microliters.
The method of borehole fluid samples has been used since the mid 1960s. Repeat Formation Tester—RFT™, developed by Schlumberger, Modular Dynamic Tester—MDT (1992) and SRFT™ (1997) are well-known. However, the Repeat Formation Tester could not perform borehole fluid analysis: it was designed for formation fluid samples transference to the surface using two high pressure cylinders equipped with remote controlled valves.
The Modular Dynamic Tester—MDT (
Borehole fluid type determination was further developed by optical fluid analyzer (OFA) module introduction. This module is introduced into the pipeline and determines the type of fluids in real time mode transmitting an intense light beam through the fluid and analyzing the spectral parameters of the transmitted light. Due to the different light absorption parameters of oil and water, this recorded spectrum shows the water and oil content and allows determining different types of oil. Gas is analyzed using various detectors that reveal gas bubbles in the reflected light. Common signal record obtained during borehole fluid type determination is shown in
However, the complexity of Modular Dynamic Tester design and of its downhole applications didn't allow borehole gas chromatography to be performed using this device.
The object of this invention is to provide a device allowing gas chromatography to be performed for in-situ borehole fluid type determination in real time mode.
The Wireline Downhole Gas Chromatograph disclosed herein is shown in
The pipeline is connected to the main pipeline of the MDT modules at the top and the bottom, since:
The method of introducing the chromatograph into the MDT device by connecting to the common (main) pipeline so that the module can be used both on the top and on the bottom of the sampling point provides flexibility of borehole tool;
The method and device for gas chromatography performing using a common pipeline allows carrying out multiple analyses in the same borehole section;
The use of OFA/LFA for chromatographic analysis preparation allows formation fluid analysis to be performed in a way to minimize fluid contamination with drilling mud and drilling mud filtrate.
The Wireline Downhole Gas Chromatograph comprises the appropriate components having the following functions:
1. The sampling valve 31 connects the MDT pipeline 30 with the chromatograph module sample chamber 32;
2. The chromatograph module sample chamber 32 is used for small portions sampling from pipeline 30 for further analysis; the sample chamber is equipped with piston position gage 42 and oil pump 41 allowing samples to be taken from the pipeline or to be placed into the pipeline.
3. The chromatograph isolating valve 33 and check valve 43 allow the sample to be transferred to the detector section of the device and prevent from sample backflow;
4. The changeable zeolite filter 34 ensures sample purity;
5. The bypass line with the bypass valve 35 are used for the removal of unwanted fluids from detector section;
6. The compressed nitrogen cylinder 36 is equipped with the transport medium valve 45 and the pressure reducer 44 that are required for establishing the transporting medium (nitrogen) flow;
7. The rotating sample injector 37 allows fluid sample to be injected in the transporting medium flow;
8. The chromatograph tube 38 in which sample fractions are separated is installed in the electric thermostat 49 that maintains the required increased temperature being regulated with the temperature sensor 47;
9. The fraction detector 39 is based on light absorption;
10. The sample portion cylinder 48 is used for after-test residual fluids gathering; and check valve 43 being installed above the detector prevents from transporting medium backflow;
11. The electronic telemetry loop 50 is used for data transfer to the surface via the wireline recorded data acquisition system.
The device operates according to the following principle:
1. The chromatograph module is located in the vicinity of the MDT bar in a way so that the formation fluid sampling point and the LFA module are at one side, and the pump module (MRPO) or other sampling equipment at the other.
2. The device is lowered into the well to the required depth, and a hydraulic contact with the formation fluids is made.
3. The formation fluids are injected by the pump, at the same time the MDT device performs resistivity, temperature and pressure measurements, and the LFA readings are taken. Once the required purity is achieved, the pumping cycle is stopped, and chromatographic analysis is initiated.
4. The sampling valve in the chromatograph module is opened, and the fluid from the pipeline is taken into the sample chamber.
5. The sampling valve is closed, and the chromatograph isolating valve is opened to supply the sample for analysis.
6. The bypass (mixing) valve is opened instantly in order to wash the contents from previous samples or other unwanted fluids.
7. The transporting medium valve is opened to form a transport medium flow.
8. The rotating sample injector is opened for injection the fluid sample for analysis.
9. The chromatograph valve is closed, and the sampling valve is opened for fluid supply from the sample fluid chamber to the pipeline. The oil pump is used for piston movement. The oil pump is stopped, and the sampling valve is closed upon the receipt of a piston position gage signal.
10. The sample is then separated in the chromatograph tube and analyzed with the detector using the standard gas chromatography method. The transporting medium residuals and the samples are supplied to the washing section.
11. Upon the completion of the analysis, the transporting medium valve is closed, and the device is ready for repeating the test at another well depth beginning from step 2 above.
The ultra small chromatographic pipes designed by the Catalysis Institute specialists of the Siberian Branch of Russian Academy of Sciences gave an opportunity to develop a device allowing to combine the gas chromatography method with oil and gas industry requirements.
The major advantage of the device claimed herein is the considerable reduction of sample processing time due to the small sizes of tubes. Analysis using the device claimed herein can be performed in a few minutes instead of several hours. This allowed the borehole gas analyzer to be developed based on the chromatography principle.
Thus, for the first time gas chromatography is used for borehole fluid type determination in the well in real time mode.
Number | Date | Country | Kind |
---|---|---|---|
2005141354 | Dec 2005 | RU | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/RU2006/000704 | 12/27/2006 | WO | 00 | 11/25/2008 |