CN108412487B - High-pressure-resistant radioactive isotope tracer and preparation method thereof - Google Patents
High-pressure-resistant radioactive isotope tracer and preparation method thereof Download PDFInfo
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- CN108412487B CN108412487B CN201810186424.XA CN201810186424A CN108412487B CN 108412487 B CN108412487 B CN 108412487B CN 201810186424 A CN201810186424 A CN 201810186424A CN 108412487 B CN108412487 B CN 108412487B
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- 239000000700 radioactive tracer Substances 0.000 title claims abstract description 66
- 230000002285 radioactive effect Effects 0.000 title claims abstract description 50
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 239000011148 porous material Substances 0.000 claims abstract description 32
- 239000011347 resin Substances 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 17
- 238000001035 drying Methods 0.000 claims abstract description 16
- 239000000853 adhesive Substances 0.000 claims abstract description 10
- 230000001070 adhesive effect Effects 0.000 claims abstract description 10
- 239000002216 antistatic agent Substances 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 239000004094 surface-active agent Substances 0.000 claims abstract description 10
- 150000002500 ions Chemical class 0.000 claims abstract description 8
- 238000001179 sorption measurement Methods 0.000 claims abstract description 8
- 239000000463 material Substances 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 31
- 239000000741 silica gel Substances 0.000 claims description 31
- 229910002027 silica gel Inorganic materials 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 25
- 230000000694 effects Effects 0.000 claims description 21
- 229910052593 corundum Inorganic materials 0.000 claims description 8
- 239000010431 corundum Substances 0.000 claims description 8
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 8
- 238000010521 absorption reaction Methods 0.000 claims description 7
- DSAJWYNOEDNPEQ-VENIDDJXSA-N barium-131 Chemical compound [131Ba] DSAJWYNOEDNPEQ-VENIDDJXSA-N 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052863 mullite Inorganic materials 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 8
- 238000011282 treatment Methods 0.000 abstract description 3
- 239000003921 oil Substances 0.000 description 20
- 238000003795 desorption Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 11
- 238000002347 injection Methods 0.000 description 10
- 239000007924 injection Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 230000003068 static effect Effects 0.000 description 9
- 238000012360 testing method Methods 0.000 description 7
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- 238000011161 development Methods 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000002791 soaking Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000002706 hydrostatic effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000012716 precipitator Substances 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B47/00—Survey of boreholes or wells
- E21B47/10—Locating fluid leaks, intrusions or movements
- E21B47/11—Locating fluid leaks, intrusions or movements using tracers; using radioactivity
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- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Geophysics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Measurement Of Radiation (AREA)
Abstract
The invention discloses a high pressure resistant radioactive isotope tracer and a preparation method thereof, and the preparation method comprises the following steps: step 1: preparing a solution containing a radioisotope; step 2: immersing the porous adsorption material into the solution, adsorbing radioactive isotope ions, and drying; and step 3: adding precipitant solution, fixing radioisotope ions with precipitant, and drying; and 4, step 4: placing the mixture in a sagger, preserving heat for 1-2 hours at a certain temperature, and naturally cooling; and 5: and sequentially treating the surface of the carrier by using a resin adhesive, an antistatic agent, a temperature resistant agent and a surfactant. After the radioactive isotope is adsorbed and fixed by the porous material carrier, the porous material carrier is subjected to high-temperature treatment, so that the pores of the porous material after the radioactive isotope is adsorbed are obviously reduced and are contracted into more compact porous balls, the pressure resistance index of the porous material is obviously improved, and the pressure resistance index of the isotope tracer is obviously improved.
Description
Technical Field
The invention relates to a preparation method of a radioactive isotope tracer, in particular to a preparation method of a high-pressure-resistant radioactive isotope tracer for water absorption profile logging.
Background
As onshore oil fields in China enter the later stage of high water content development, the pressure of an oil layer is gradually reduced, and in order to realize long-term stable development, energy needs to be supplemented to the stratum and the pressure of the oil layer needs to be maintained, so that the aim of improving the yield of crude oil by 'displacing oil with water' is fulfilled. Therefore, in oil field development, a lot of water injection wells are drilled in addition to a lot of oil production wells, and individual wells with high water content are changed to water injection wells after a period of production. And injecting water into the underground oil layer through the water injection well to maintain the pressure of the oil layer, so that the recovery ratio of the crude oil is improved. Water injection monitoring is the key of 'displacement of reservoir oil with water' failure, and the monitoring uncertainty can influence the utilization of petroleum resources and even can cause major accidents, such as 'Kangfei oil leakage' accident of Bohai sea. In addition, after the oil field enters the middle and later stages, the water injection cost is greatly increased along with the multiple increase of the water injection quantity. Therefore, the waterflood indexes play more and more important roles in measuring the oil reservoir development effect. However, due to the differences in the geological conditions of the various fields, the formation conditions of even the same reservoir are quite complex. How to inject water can achieve the best development effect is always one of the focus problems concerned by oil field logging.
The radioactive isotope tracing method is the most common method for acquiring water absorption profile information at present in an oil field. During logging, the radioactive isotope tracer is released at a specified depth, the tracer and the borehole injection form an activated suspension, and when the selected tracer diameter is equal to the pore diameter of the formation, the injection in the suspension enters the formation, and the tracer is filtered and deposited on the borehole wall. The injection amount of the stratum, the tracer amount accumulated on the section of stratum well wall and the radioactive intensity of the tracer are in a direct proportion relation, and water injection information can be calculated and obtained by comparing gamma logging curves measured before and after the formation accumulation by the tracer. Compared with other well logging methods, the radioactive isotope tracing well logging method has the advantages of high sensitivity, simplicity and convenience in method, accuracy in positioning and quantification and the like. However, the existing isotope tracer products have a prominent problem that the pressure resistance is low (less than or equal to 60 MPa). At present, as onshore oil fields in China successively enter the middle and later periods of exploitation, oil production wells become deeper and deeper, geological environments become more and more complex, and higher requirements are put forward on the pressure resistance of isotope tracers. The existing isotope tracer agent can be broken due to low pressure resistance when in use, so that the problems of easy desorption of the isotope, small particle size of the tracer agent and the like are caused, and when the particle size of the tracer agent is smaller than the pore of a stratum, the tracer agent can enter the stratum along with water instead of being accumulated on a well wall, so that finally, the acquired logging information is inaccurate or even wrong.
Disclosure of Invention
The invention aims to provide a high-pressure resistant radioactive isotope tracer and a preparation method thereof aiming at the defects of the prior art.
A preparation method of a high pressure resistant radioactive isotope tracer agent comprises the following steps:
step 1: preparing a solution containing a radioisotope;
step 2: immersing the porous adsorption material into the solution, adsorbing radioactive isotope ions, and drying;
and step 3: adding precipitant solution, fixing radioisotope ions with precipitant, and drying;
and 4, step 4: placing the mixture in a sagger, preserving heat for 1-2 hours at high temperature, and naturally cooling;
and 5: and sequentially treating the surface of the carrier by using a resin adhesive, an antistatic agent, a temperature resistant agent and a surfactant, and drying to obtain the high-pressure resistant radioisotope tracer for water absorption profile logging.
The method, the radioactive isotope in the step (1) is barium-131; the preparation method of the solution containing the radioactive isotope comprises the steps of directly dissolving carbonate containing barium-131 by acid;
in the method, the concentration of acid used for dissolving carbonate is 40-70% of perchloric acid or 10-20% of nitric acid.
In the method, the porous adsorption material in the step (2) is coarse-pore silica gel; the particle size of the coarse-pore silica gel is 200-400 μm.
In the method, the precipitating agent in the step (3) is soluble salt which can form a difficultly soluble substance with radioactive isotope ions, and the soluble salt comprises carbonate or sulfate.
The method comprises the steps that in the step (2) and the step (3), the drying temperature is 100-300 ℃;
in the method, the sagger in the step (4) is a corundum sagger, a silicon carbide sagger, a mullite sagger or other high-temperature saggers with the highest temperature resistance higher than 1500 ℃.
In the method, the heat preservation temperature in the step (4) is 1000-1400 ℃.
According to the method, the specific radioactivity of the high-pressure resistant radioisotope tracer prepared in the step (5) is 0.15-6.32 (E +6 Bq)/g.
A radioisotope tracer prepared according to any one of the methods.
In order to better utilize the adsorbability of a porous material to adsorb radioactive isotopes, the conventional preparation process of the radioactive isotope tracer mainly adopts a porous material with high porosity and large specific surface area, and the pressure resistance of the porous material with stronger adsorption performance is lower, so that the pressure resistance of a porous material carrier is generally sacrificed in the conventional process. Compared with the existing preparation process of the radioactive isotope tracer, the preparation process disclosed by the invention has the advantages that after the radioactive isotope is adsorbed and fixed by the porous material carrier, the porous material is subjected to high-temperature treatment, so that the pores of the porous material after the radioactive isotope is adsorbed are obviously reduced and are contracted into more compact porous small balls, and further the pressure resistance index of the porous material is obviously improved, the problem that the adsorbability and the pressure resistance of the porous adsorbing material carrier in the existing preparation process of the radioactive isotope tracer cannot be simultaneously solved, and finally, the pressure resistance index of the isotope tracer is obviously improved, so that the preparation process is more suitable for oil and gas exploitation in medium-deep wells and complex geological exploitation environments.
Detailed Description
The technical solution of the present invention is further described in detail with reference to the following embodiments, but the scope of the present invention is not limited thereto.
Embodiment 1:
step 1: dissolving barium carbonate with activity of 7.16(E +8Bq) and containing radioactive isotope barium-131 in 25ml of 10% nitric acid, and diluting to 500 ml;
step 2: then weighing 400g of coarse-pore silica gel with the particle size of 200-400 mu m, adding the coarse-pore silica gel into the solution in the step (1), stirring the mixture for 3 hours at the temperature of 100-300 ℃, and drying the mixture;
and step 3: adding 150ml of 5% sodium carbonate solution, stirring at the temperature of 100-300 ℃ for 2 hours, and drying;
and 4, step 4: placing a porous silica gel carrier for absorbing the radioactive isotope in a corundum sagger, then placing the corundum sagger in a KSL-1700X-A4 box-type furnace, and preserving heat for 2 hours at 1100 ℃;
and 5: and sequentially treating the surface of the porous silica gel carrier by using resin adhesive, an antistatic agent, temperature-resistant resin and a surfactant. The resin adhesive is used for plugging holes on the surface of the porous silica gel, and is used for regulating the specific gravity of the tracer together with the precipitator and preventing the desorption of the tracer; the antistatic agent is used for removing static electricity generated by mutual friction of the tracers; the temperature-resistant resin can enhance the high-temperature stability of the tracer; surfactants are used to enhance the hydrophilicity of the tracer surface.
For example, the following treatments are performed in order: adding 400ml of resin adhesive, rotating at 60 ℃ for 20min-1Stirring for 9 hours; ② antistatic agent 1g, 80 ℃, rotating speed 20min-1Stirring for 2 hours; ③ 400ml of temperature-resistant resin, 100 ℃ and 30min of rotating speed-1Stirring for 8 hours; fourthly, 60ml of surface active agent with the rotating speed of 25min at 75 DEG C-1Stirring for 6 h.
After the surface treatment is carried out on the porous silica gel carrier absorbing the radioactive isotope, the high-pressure resistant radioactive isotope tracer for water absorption profile logging is prepared.
The obtained radioisotope tracer is soaked in distilled water for 2 hr to obtain specific gravity of 1.03g/cm3(ii) a After being put into a polyester textile bag, the tracer is put into a hydrostatic test device, the pressure is increased to 90MPa, and the breaking rate is 4.8%; specific activity of 1.01(E +6Bq)/cm3(ii) a Taking 20mCi tracer, measuring the activity change of the tracer before and after soaking in normal temperature distilled water for 24h by using an activity meter, wherein the static desorption rate is 4.8%; the 20mCi tracer is taken, the activity change of the tracer in water flow at 75 ℃ for 24 hours is measured by an activity meter, and the dynamic desorption rate is 9.3%. The same porous silica gel carrier, without high temperature heat treatment, was crushed at 60MPa according to the same test methodThe rate is 5%, the static desorption rate is 5.2%, and the dynamic desorption rate is 10.5%. The comparison of the test results shows that the porous silica gel carrier is heated at high temperature after adsorbing and fixing the radioactive isotope, so that the pressure resistance index of the radioactive isotope tracer can be obviously improved without influencing the adsorption performance of the isotope, and the porous silica gel carrier is more suitable for oil gas exploitation in medium-deep wells and complex geological exploitation environments.
Embodiment 2:
step 1: barium carbonate with activity 8.59(E +8Bq) containing the radioisotope barium-131 was dissolved in 30ml of 40% perchloric acid and diluted to 500 ml;
step 2: then weighing 400g of coarse-pore silica gel with the particle size of 200-400 mu m, adding the coarse-pore silica gel into the solution in the step (1), stirring the mixture at the temperature of 100-300 ℃ for 2 hours, and drying the mixture;
and step 3: adding 250ml of 2% sodium sulfate solution, stirring at the temperature of 100-300 ℃ for 2 hours, and drying;
and 4, step 4: placing a porous silica gel carrier for absorbing the radioactive isotope in a corundum sagger, then placing the corundum sagger in a KSL-1700X-A4 box-type furnace, and keeping the temperature at 1200 ℃ for 1.5 h;
and 5: and sequentially treating the surface of the porous silica gel carrier by using resin adhesive, an antistatic agent, temperature-resistant resin and a surfactant. The resin adhesive is used for plugging holes on the surface of the porous silica gel, and is used for regulating the specific gravity of the tracer together with the precipitator and preventing the desorption of the tracer; the antistatic agent is used for removing static electricity generated by mutual friction of the tracers; the temperature-resistant resin can enhance the high-temperature stability of the tracer; surfactants are used to enhance the hydrophilicity of the tracer surface. After the surface treatment is carried out on the porous silica gel carrier absorbing the radioactive isotope, the high-pressure resistant radioactive isotope tracer for water absorption profile logging is prepared.
The obtained radioisotope tracer is soaked in distilled water for 2 hr to obtain specific gravity of 1.04g/cm3(ii) a After being put into a polyester textile bag, the tracer is put into a hydrostatic test device, the pressure is increased to 90MPa, and the breaking rate is 4.3%; the specific activity of the radioactivity is 1.21(E +6Bq)/cm3(ii) a Taking 20mCi tracer, measuring activity change of tracer before and after soaking in distilled water at normal temperature for 24h by using activity meterThe static desorption rate is 4.5%; the activity change of 20mCi tracer in water flow at 75 deg.c for 24 hr is measured with activity meter and the dynamic desorption rate is 8.7%. The same porous silica gel carrier, without high temperature heat treatment, was directly subjected to the above steps to obtain the radioisotope tracer, according to the same test method, at 60MPa, the breakage rate was 5%, the static desorption rate was 5.2%, and the dynamic desorption rate was 10.5%. The comparison of the test results shows that the porous silica gel carrier is heated at high temperature after adsorbing and fixing the radioactive isotope, so that the pressure resistance index of the radioactive isotope tracer can be obviously improved without influencing the adsorption performance of the isotope, and the porous silica gel carrier is more suitable for oil gas exploitation in medium-deep wells and complex geological exploitation environments.
Embodiment 3:
step 1: barium carbonate with activity 8.33(E +8Bq) containing the radioisotope barium-131 was dissolved in 30ml of 70% perchloric acid and diluted to 500 ml;
step 2: then weighing 400g of coarse-pore silica gel with the particle size of 200-400 mu m, adding the coarse-pore silica gel into the solution in the step (1), stirring the mixture at the temperature of 100-300 ℃ for 2 hours, and drying the mixture;
and step 3: adding 200ml of 2% sodium sulfate solution, stirring at the temperature of 100-300 ℃ for 2 hours, and drying;
and 4, step 4: placing a porous silica gel carrier for absorbing the radioactive isotope in a corundum sagger, then placing the corundum sagger in a KSL-1700X-A4 box-type furnace, and preserving heat for 1h at 1300 ℃;
and 5: and sequentially treating the surface of the porous silica gel carrier by using resin adhesive, an antistatic agent, temperature-resistant resin and a surfactant. The resin adhesive is used for plugging holes on the surface of the porous silica gel, and is used for regulating the specific gravity of the tracer together with the precipitator and preventing the desorption of the tracer; the antistatic agent is used for removing static electricity generated by mutual friction of the tracers; the temperature-resistant resin can enhance the high-temperature stability of the tracer; surfactants are used to enhance the hydrophilicity of the tracer surface. After the surface treatment is carried out on the porous silica gel carrier absorbing the radioactive isotope, the high-pressure resistant radioactive isotope tracer for water absorption profile logging is prepared.
Distillation of the prepared radiotracerAfter soaking in water for 2h, the specific gravity was measured to be 1.05g/cm3(ii) a After being put into a polyester textile bag, the tracer is put into a hydrostatic test device, the pressure is increased to 90MPa, and the breaking rate is 4.0%; the specific activity of the radioactivity is 1.17(E +6Bq)/cm3(ii) a Taking 20mCi tracer, measuring the activity change of the tracer before and after soaking in normal temperature distilled water for 24h by using an activity meter, wherein the static desorption rate is 4.3%; the activity change of 20mCi tracer in water flow at 75 deg.c for 24 hr is measured with activity meter and the dynamic desorption rate is 8.1%. The same porous silica gel carrier, without high temperature heat treatment, was directly subjected to the above steps to obtain the radioisotope tracer, according to the same test method, at 60MPa, the breakage rate was 5%, the static desorption rate was 5.2%, and the dynamic desorption rate was 10.5%. The comparison of the test results shows that the porous silica gel carrier is heated at high temperature after adsorbing and fixing the radioactive isotope, so that the pressure resistance index of the radioactive isotope tracer can be obviously improved without influencing the adsorption performance of the isotope, and the porous silica gel carrier is more suitable for oil gas exploitation in medium-deep wells and complex geological exploitation environments.
It will be understood that modifications and variations can be made by persons skilled in the art in light of the above teachings and all such modifications and variations are intended to be included within the scope of the invention as defined in the appended claims.
Claims (11)
1. A preparation method of a high pressure resistant radioactive isotope tracer agent is characterized by comprising the following steps:
step 1: preparing a solution containing a radioisotope;
step 2: immersing the porous material into the solution obtained in the step (1), adsorbing radioactive isotope ions, and drying;
and step 3: adding a precipitant solution into the dried product obtained in the step (2), fixing radioisotope ions by using the precipitant, and drying to obtain a porous material for adsorbing the radioisotope;
and 4, step 4: placing the porous material for adsorbing the radioactive isotope in a sagger, preserving heat for 1-2 hours at high temperature, and naturally cooling to obviously reduce the pores of the porous material for adsorbing the radioactive isotope;
and 5: and sequentially treating the surface of the porous material by using a resin adhesive, an antistatic agent, a temperature resistant agent and a surfactant, and drying to obtain the high-pressure resistant radioactive isotope tracer for water absorption profile logging.
2. The method of claim 1, wherein: the radioactive isotope in the step (1) is barium-131; the preparation method of the solution containing the radioactive isotope is to directly dissolve carbonate containing barium-131 by acid.
3. The method of claim 2, wherein: the acid used for dissolving the carbonate has the concentration of 40-70% perchloric acid or 10-20% nitric acid.
4. The method of claim 1, wherein: the porous adsorption material in the step (2) is coarse-pore silica gel; the particle size of the coarse-pore silica gel is 200-400 μm.
5. The method of claim 1, wherein: the precipitant in the step (3) is soluble salt which can form insoluble matters with radioactive isotope ions, and comprises carbonate or sulfate.
6. The method of claim 1, wherein: and (3) drying at 100-300 ℃.
7. The method of claim 1, wherein: and (4) the sagger is a high-temperature sagger with the highest temperature resistance higher than 1500 ℃.
8. The method of claim 7, wherein: the high-temperature sagger is a corundum sagger, a silicon carbide sagger or a mullite sagger.
9. The method according to claim 1 or 4, characterized in that: and (4) keeping the temperature of 1000-1400 ℃.
10. The method of claim 1, wherein: the radioactive specific activity of the high-pressure resistant radioactive isotope tracer prepared in the step (5) is 0.15-6.32 (E +6 Bq)/g.
11. A radiotracer prepared according to the method of any one of claims 1 to 10.
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CN114233282A (en) * | 2021-12-22 | 2022-03-25 | 河南省科学院同位素研究所有限责任公司 | High-efficient zero radioactivity emission well logging tracer preparation system |
CN114837656A (en) * | 2022-05-23 | 2022-08-02 | 河南省科学院同位素研究所有限责任公司 | Preparation method of density controllable isotope carrier |
CN117072144B (en) * | 2023-06-27 | 2024-05-28 | 河南省科学院同位素研究所有限责任公司 | Preparation device and method of radioactive isotope tracer for injection profile logging |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1081491A (en) * | 1992-07-15 | 1994-02-02 | 中国核动力研究设计院 | A kind of survey of wells by radioactive isotope tracking method |
WO2001081914A1 (en) * | 2000-04-26 | 2001-11-01 | Sinvent As | Reservoir monitoring |
CN102182442A (en) * | 2011-03-10 | 2011-09-14 | 河南省科学院同位素研究所有限责任公司 | Method for preparing radioisotope tracer |
CN102304358A (en) * | 2011-07-12 | 2012-01-04 | 原子高科股份有限公司 | Radiolabeled coated ceramsite supporting agent and preparation method thereof |
CN102445389A (en) * | 2011-09-22 | 2012-05-09 | 河南省科学院同位素研究所有限责任公司 | Pressure testing method for radioactive isotope carrier |
WO2012166448A1 (en) * | 2011-05-31 | 2012-12-06 | 3M Innovative Properties Company | Retroreflective articles having composite cube-corners and methods of making |
CN103343684A (en) * | 2013-06-18 | 2013-10-09 | 中国石油天然气股份有限公司 | Complex tracer agent for oil field high-temperature hypersalinity block interwell monitoring and application thereof |
CN103738959A (en) * | 2014-02-19 | 2014-04-23 | 南京大学 | C-14-marked graphene and synthetic method thereof |
CN104514542A (en) * | 2013-10-07 | 2015-04-15 | 天津大港油田圣达科技有限公司 | Method for interwell monitoring through stable isotope 18O |
CN104563975A (en) * | 2014-12-24 | 2015-04-29 | 中国石油天然气股份有限公司 | Gravel packing effect detecting method and detecting device by adopting isotopic tracing |
CN105849366A (en) * | 2013-11-05 | 2016-08-10 | 光谱追踪服务有限公司 | Method and composition for hydraulic fracturing and fr tracing petroleum production |
WO2017125854A1 (en) * | 2016-01-19 | 2017-07-27 | Research Triangle Institute | Methods and materials for controlled release of desired chemistries |
WO2017184571A1 (en) * | 2016-04-20 | 2017-10-26 | Spectrum Tracer Services, Llc | Method and compositions for hydraulic fracturing and for tracing formation water |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1970916B1 (en) * | 2006-05-18 | 2015-04-01 | Hitachi Metals, Ltd. | R-Fe-B POROUS MAGNET AND METHOD FOR PRODUCING THE SAME |
US20150245547A1 (en) * | 2014-02-24 | 2015-08-27 | William L. Robinson, Jr. | Method and use of organic and mineral admixtures for EMI and radioisotope shielding of air filtration media and building materials, for absorption of airborne particulates and for climate change mitigation |
CN104575626B (en) * | 2014-12-19 | 2017-06-06 | 清华大学 | For the spike microballoon of pebble bed high temperature reactor |
US9910026B2 (en) * | 2015-01-21 | 2018-03-06 | Baker Hughes, A Ge Company, Llc | High temperature tracers for downhole detection of produced water |
US20180094185A1 (en) * | 2015-04-22 | 2018-04-05 | Halliburton Energy Services, Inc. | Cellulose or Cellulose Derivative Including Grafted Acrylamide or Acrylic Acid Groups for Treatment of Subterranean Formations |
GB201615517D0 (en) * | 2016-09-13 | 2016-10-26 | Micromatrices Ass L | Spheroid tissue miroarray and method of manufacture |
-
2018
- 2018-03-07 CN CN201810186424.XA patent/CN108412487B/en active Active
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1081491A (en) * | 1992-07-15 | 1994-02-02 | 中国核动力研究设计院 | A kind of survey of wells by radioactive isotope tracking method |
WO2001081914A1 (en) * | 2000-04-26 | 2001-11-01 | Sinvent As | Reservoir monitoring |
CN102182442A (en) * | 2011-03-10 | 2011-09-14 | 河南省科学院同位素研究所有限责任公司 | Method for preparing radioisotope tracer |
WO2012166448A1 (en) * | 2011-05-31 | 2012-12-06 | 3M Innovative Properties Company | Retroreflective articles having composite cube-corners and methods of making |
CN102304358A (en) * | 2011-07-12 | 2012-01-04 | 原子高科股份有限公司 | Radiolabeled coated ceramsite supporting agent and preparation method thereof |
CN102445389A (en) * | 2011-09-22 | 2012-05-09 | 河南省科学院同位素研究所有限责任公司 | Pressure testing method for radioactive isotope carrier |
CN103343684A (en) * | 2013-06-18 | 2013-10-09 | 中国石油天然气股份有限公司 | Complex tracer agent for oil field high-temperature hypersalinity block interwell monitoring and application thereof |
CN104514542A (en) * | 2013-10-07 | 2015-04-15 | 天津大港油田圣达科技有限公司 | Method for interwell monitoring through stable isotope 18O |
CN105849366A (en) * | 2013-11-05 | 2016-08-10 | 光谱追踪服务有限公司 | Method and composition for hydraulic fracturing and fr tracing petroleum production |
CN103738959A (en) * | 2014-02-19 | 2014-04-23 | 南京大学 | C-14-marked graphene and synthetic method thereof |
CN104563975A (en) * | 2014-12-24 | 2015-04-29 | 中国石油天然气股份有限公司 | Gravel packing effect detecting method and detecting device by adopting isotopic tracing |
WO2017125854A1 (en) * | 2016-01-19 | 2017-07-27 | Research Triangle Institute | Methods and materials for controlled release of desired chemistries |
WO2017184571A1 (en) * | 2016-04-20 | 2017-10-26 | Spectrum Tracer Services, Llc | Method and compositions for hydraulic fracturing and for tracing formation water |
Non-Patent Citations (1)
Title |
---|
一种新型同位素示踪剂载体及应用;李勇;《测井技术》;20030520;第27卷(第5期);第427-431页 * |
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