CN114837656A - Preparation method of density controllable isotope carrier - Google Patents

Preparation method of density controllable isotope carrier Download PDF

Info

Publication number
CN114837656A
CN114837656A CN202210565022.7A CN202210565022A CN114837656A CN 114837656 A CN114837656 A CN 114837656A CN 202210565022 A CN202210565022 A CN 202210565022A CN 114837656 A CN114837656 A CN 114837656A
Authority
CN
China
Prior art keywords
density
controllable
preparing
isotope
pigment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN202210565022.7A
Other languages
Chinese (zh)
Inventor
张本尚
华道本
陈海军
范家霖
邓刚
张悦
王晓慧
董明静
管晖
孟闯
李旭照
张奕
黎振华
李甜甜
杨淑蕊
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henan Tongxin Technology Co ltd
Isotope Institute Co ltd Of Henan Academy Of Sciences
Original Assignee
Henan Tongxin Technology Co ltd
Isotope Institute Co ltd Of Henan Academy Of Sciences
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henan Tongxin Technology Co ltd, Isotope Institute Co ltd Of Henan Academy Of Sciences filed Critical Henan Tongxin Technology Co ltd
Priority to CN202210565022.7A priority Critical patent/CN114837656A/en
Priority to CN202210883288.6A priority patent/CN114991759B/en
Publication of CN114837656A publication Critical patent/CN114837656A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B47/00Survey of boreholes or wells
    • E21B47/10Locating fluid leaks, intrusions or movements
    • E21B47/11Locating fluid leaks, intrusions or movements using tracers; using radioactivity
    • E21B47/111Locating fluid leaks, intrusions or movements using tracers; using radioactivity using radioactivity
    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/20Displacing by water

Abstract

The invention provides a preparation method of a density controllable isotope carrier, which comprises the following steps: s1, fully mixing the activated carbon powder, the resin powder, the hollow glass beads and the pigment in a V-shaped mixer according to a certain proportion; s2, fully mixing the adhesive and the obtained mixture in a certain proportion in a high-speed mixer; s3, transferring to a swing granulator for granulation; s4, rounding the product in a rounding machine for a period of time and then drying; s5 and then sieving through different particle size ranges as required. The invention has the following beneficial effects: wide density regulating range, high heat resistance, high strength, high isotope adsorption, easy material obtaining and simple process.

Description

Preparation method of density controllable isotope carrier
Technical Field
The invention belongs to the technical field of oil field monitoring, and particularly relates to a preparation method of a density-controllable isotope carrier.
Background
The oil field is developed for a long time to cause the continuous decline of stratum energy (pressure), the exploitation difficulty is more and more big, and oil displacement technologies such as water injection, gas injection, steam injection, polymer injection and the like are adopted to improve the recovery ratio and the recovery efficiency of residual oil, wherein the water injection and the oil displacement account for a larger proportion. The injected water flows through the stratum to bring the crude oil in the stratum to the oil production well and then is produced by the oil production machine, the produced mixture is separated, the crude oil in the mixture is sent to the oil refinery, the injected water is reused to be injected into the ground, and more oil is produced in a circulating way.
The establishment of the injection and production scheme is the key of residual oil exploitation, and the dynamic injection monitoring provides decision basis for analyzing the relation between injection and oil production and the establishment of the injection and production scheme, and is leading work. The existing injection monitoring technology comprises a noise instrument, a heat flow instrument, pulse neutron oxygen activation, a turbine flowmeter, an isotope tracing method and the like, wherein the isotope tracing method has the advantages of obvious layering, no influence of a pipe column, simple and effective method, low cost and the like and is widely adopted by oil fields. Isotopic tracing methods are mainly of two types: correlated flow logs and injection profile logs. The isotope tracer used for the related flow logging is liquid, and the principle is that the isotope tracer is released above the water absorption layer of the water injection well, the tracer flows along with water, a detection instrument tracks ray signals to obtain the flow velocity information of injected water, when the tracer passes through the water absorption layer, a part of the tracer enters the stratum along with the water, the flow velocity of the injected water is reduced, and the detection instrument records the change, so that the injection dynamics of each water absorption layer can be obtained. The injection profile well logging, also called three-parameter or five-parameter well logging, etc. adopts the principle that the adopted radioactive isotope tracer is solid particles, and is released above the water-absorbing layer of the water injection well, the tracer can be flowed with injected water, and after the tracer is reached to the water-absorbing layer, the water can be fed into stratum, the tracer can be filtered and deposited on the surface of the water-absorbing layer, the gamma ray emitted by radioactive isotope can be detected by detection instrument so as to obtain stratum position, at the same time the ray strength can be correspondent to the water injection quantity of said position, so that the injection condition of every water-absorbing layer can be obtained.
In the oil field radioactive isotope tracing well logging, the injection profile well logging accounts for about 70%, the used radioactive isotope tracer is spherical solid particles, the method of patent CN201110057628.1 is usually adopted for preparation, and the carrier for loading isotope is usually silica gel or active carbon. With the improvement of the technical level and the refinement degree of the oil field logging, the density of the solid tracer is not required to be uniform any more, and the density of the tracer is required to be determined according to factors such as a logging process, the formation condition of the oil field, the mineralization degree of injected water and the like. The density of the existing isotope carrier is fixed, and the tracer density is finely adjusted by simply utilizing a surface treatment method, so that the oil field logging requirement cannot be met. Therefore, a new carrier preparation method is invented to meet the preparation requirement of the solid tracer.
Disclosure of Invention
In order to solve the above problems, the present invention provides a method for preparing a density-controllable isotope carrier.
The invention relates to a preparation method of a density controllable isotope carrier, which comprises the following steps:
s1, fully mixing the activated carbon powder, the resin powder, the hollow glass beads and the pigment in a V-shaped mixer according to a certain proportion;
s2, fully mixing the adhesive and the obtained mixture in a certain proportion in a high-speed mixer;
s3, transferring to a swing granulator for granulation;
s4, rounding the product in a rounding machine for a period of time and then drying;
s5 and then sieving through different particle size ranges as required.
Preferably, the activated carbon powder, the resin powder and the pigment are powdery, and the fineness of the activated carbon powder, the resin powder and the pigment is 20-600 meshes.
Preferably, the resin powder is poly 4-methyl-1-pentene or polypropylene; the pigment is inorganic or organic pigment such as carbon black.
Preferably, the mass ratio of the activated carbon powder, the resin powder, the hollow glass beads and the pigment is 0-70: 0-90: 0-90: 0-50.
Preferably, the mixing is carried out in the V-shaped mixer for 10 to 30 minutes.
Preferably, the mixture is fully mixed in the high-speed mixer, the shearing rotating speed is 0-500 r/min, the mixing rotating speed is 0-200 r/min, and the mixing time is 10-30 min.
Preferably, the adhesive is (1) a cyclohexane solution of poly 4-methyl-1-pentene or polypropylene; (2) ethyl cellulose, methyl cellulose, polyacrylic resin or polyvinyl butyral ethanol solution; (3) an aqueous solution of polyvinyl alcohol; (4) ethyl acetate solution of polyvinyl butyral, ethyl acetate solution of epoxy resin and curing agent, or ethyl acetate solution of polyurethane prepolymer and polyol, or a mixture of two binders of (1), (2) and (4).
Preferably, the screen used in the swing granulator is 5 to 80 mesh.
Preferably, the rounding machine is used for rounding, the rounding rotating speed is 0-300 r/min, the air flow speed is 0-100m3/h, the time is controlled to be 1-20 min, and the adhesive or the solvent of the adhesive is added in the rounding process, and the adding amount is 0-20% of the total material amount.
Preferably, the drying process can adopt a fluidized drying machine, the drying temperature is 30-90 ℃, and the air flow speed is 0-1500m3/h, and the drying time is 0.1-3 hours.
The preparation method of the density controllable isotope carrier has the following beneficial effects: wide density regulating range, high heat resistance, high strength, high isotope adsorption, easy material obtaining and simple process.
Detailed Description
In order that the invention may be better understood, the following further description is provided, taken in conjunction with the accompanying examples, so that the advantages and features of the invention will be more readily understood by those skilled in the art. It should be noted that the following description is only a preferred embodiment of the present invention, but the present invention is not limited to the following embodiment. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. For instance, features illustrated or described as part of one embodiment, can be used with another embodiment to yield a still further embodiment. Therefore, it is intended that the present invention encompass such modifications and variations within the scope of the appended claims and their equivalents.
The invention provides a preparation method of a density controllable isotope carrier, which comprises the following steps:
s1, fully mixing the activated carbon powder, the resin powder, the hollow glass beads and the pigment in a V-shaped mixer according to a certain proportion;
s2, fully mixing the adhesive and the obtained mixture in a certain proportion in a high-speed mixer;
s3, transferring to a swing granulator for granulation;
s4, rounding the product in a rounding machine for a period of time and then drying;
s5 and then sieving through different particle size ranges as required.
The method can obtain particles with the density of 0.2-1.5g/ml and the diameter of 100-10000 microns, and is suitable for oil field isotope tracing well logging.
Preferably, the activated carbon powder, the resin powder and the pigment are powdery, the fineness is 20-600 meshes, and the fineness is preferably 80-120 meshes from the aspect of dust control.
Preferably, the resin powder is poly-4-methyl-1-pentene or polypropylene; the pigment is inorganic or organic pigment such as carbon black.
Preferably, the mass ratio of the activated carbon powder, the resin powder, the hollow glass beads and the pigment is 0-70: 0-90: 0-90: 0-50.
Preferably, the mixture is fully mixed in the V-shaped mixer, and the preferable time is 10 to 30 minutes;
preferably, the materials are fully mixed in the high-speed mixer, and the preferred shearing rotating speed is 0-500 r/min, the mixing rotating speed is 0-200 r/min, and the mixing time is 10-30 min;
preferably, the adhesive is (1) a cyclohexane solution of poly 4-methyl-1-pentene or polypropylene; (2) ethyl cellulose, methyl cellulose, polyacrylic resin or polyvinyl butyral ethanol solution; (3) an aqueous solution of polyvinyl alcohol; (4) ethyl acetate solution of polyvinyl butyral, ethyl acetate solution of epoxy resin and curing agent, or ethyl acetate solution of polyurethane prepolymer and polyol, or a mixture of two binders of (1), (2) and (4). The solid content of the adhesive is 1-20%, and the addition amount of the adhesive is 10-50% of the total material amount.
Preferably, the screens used in the swing granulator are of 5 to 80 mesh, preferably 16 mesh, 20 mesh and 28 mesh.
Preferably, the rounding machine is used for rounding, the rounding rotating speed is 0-300 r/min, the air flow speed is 0-100m3/h, the time is controlled to be 1-20 min, and the adhesive or the solvent of the adhesive in 7 is added in the rounding process, and the adding amount is 0-20% of the total material amount.
Preferably, the drying process can adopt a fluidized drying machine, the drying temperature is 30-90 ℃, and the air flow speed is 0-1500m3/h, and the drying time is 0.1-3 hours.
Preferably, the sieving particle size range is usually 0-100 μm, 100-450 μm, 450-750 μm, 750-1000 μm, 1000-1500 μm, 1500-2000 μm, 2000-5000 μm, 5000-10000 μm, etc.
Example 1
0.1Kg of 150 mesh activated carbon powder, 0.8Kg of 80 mesh polypropylene powder, and 0.1Kg of 600 mesh carbon black were mixed in a V-type mixer for 25 minutes. The mixture is transferred to a high-speed mixer, 900ml of a 10% strength ethyl acetate solution of polyvinyl butyral are added at a mixing speed of 30 rpm and a shear speed of 60 rpm, and after the addition, the mixture is mixed for 30 minutes at a mixing speed of 120 rpm and a shear speed of 180 rpm. Putting the product into a swing granulator, using a sieve with 24 meshes, putting the sieved product into a spheronizer to be spheronized, wherein the rotating speed is 60 revolutions per minute, the air flow speed is 0-20m3/h, simultaneously adding 500ml of ethanol uniformly within 10 minutes, spheronizing for 10 minutes, and discharging. The obtained product was dried in a fluidized drier at an air flow rate of 800m for 2 hours 3 H, the drying temperature is 65 ℃. Separating the dried product by using a rotary vibration sieve according to the particle size ranges of 0-100 μm, 100-450 μm, 450-750 μm, 750-1000 μm, 1000-1500 μm and 1500-2000 μm to obtain the finished product.
The density of the existing silica gel carrier is mainly between 0.99 and 1.02g/ml, the density of the active carbon carrier is larger and is usually more than 1.2g/ml, and the carrier can be controlled between 0.2 and 1.2g/ml, thereby fully meeting the technical requirements of monitoring water injection, gas (steam) injection and polymer injection in oil fields. The resin powder and the hollow glass beads can reduce the density of the carrier, if only the activated carbon powder is added, the resin powder or the hollow glass beads are not added, the density of the obtained carrier is about 1.5g/ml, if 50% of the resin powder is added, the density of the obtained carrier is 1.0-1.15g/ml, and if 20% of the hollow glass beads are added, the density of the obtained carrier is 1.05-1.2 g/ml. Pigments can perform two functions: firstly, adjust carrier density, secondly can use the carrier of different densities of different colour sign, make the user use more convenient.
Logging conditions such as oilfield logging process, injection water pressure, temperature, degree of mineralization and the like are different, and different carrier densities are required, such as logging-on and logging-back, and the density is lower than 1g/ml, for example, 0.98g/ml may be more suitable. If the injected water has a high degree of mineralization and the density of the water is high, such as 1.02g/ml, it is more appropriate to select a carrier having a density of 1.02 g/ml.
The preparation method of the density controllable isotope carrier has the following beneficial effects: wide density regulating range, high heat resistance, high strength, high isotope adsorption, easy material obtaining and simple process.
All equivalent or simple changes of the structure, the characteristics and the principle of the invention which are described in the patent conception of the invention are included in the protection scope of the patent of the invention. Various modifications, additions and substitutions for the specific embodiments described may be made by those skilled in the art without departing from the scope of the invention as defined in the accompanying claims.

Claims (10)

1. A method for preparing a density-controllable isotope carrier, the method comprising:
s1, fully mixing the activated carbon powder, the resin powder, the hollow glass beads and the pigment in a V-shaped mixer according to a certain proportion;
s2, fully mixing the adhesive and the obtained mixture in a certain proportion in a high-speed mixer;
s3, transferring to a swing granulator for granulation;
s4, rounding the product in a rounding machine for a period of time and then drying;
s5 and then sieving through different particle size ranges as required.
2. The method for preparing a density controllable isotope carrier of claim 1 wherein the activated carbon powder, resin powder, and pigment are in the form of powders with a fineness of 20-600 mesh.
3. The method for preparing a density-controllable isotope carrier according to claim 2, wherein the resin powder is poly-4-methyl-1-pentene or polypropylene; the pigment is inorganic or organic pigment such as carbon black.
4. The method for preparing a density-controllable isotope carrier according to claim 3, wherein the mass ratio of the activated carbon powder, the resin powder, the hollow glass beads and the pigment is 0-70: 0-90: 0-90: 0-50.
5. A method for preparing a density controllable isotopic carrier as claimed in claim 4, wherein mixing is effected in said V-blender for a time period of 10 to 30 minutes.
6. A method for preparing a density controllable isotopic carrier as claimed in claim 1, wherein mixing is effected in said high speed mixer at a shear rate of 0 to 500 rpm for a mixing time of 10 to 30 minutes at a mixing rate of 0 to 200 rpm.
7. The method for preparing a density-controllable isotope carrier according to claim 1, wherein said binder is (1) a cyclohexane solution of poly-4-methyl-1-pentene or polypropylene; (2) ethyl cellulose, methyl cellulose, polyacrylic resin or polyvinyl butyral ethanol solution; (3) an aqueous solution of polyvinyl alcohol; (4) ethyl acetate solution of polyvinyl butyral, ethyl acetate solution of epoxy resin and curing agent, or ethyl acetate solution of polyurethane prepolymer and polyol, or a mixture of two binders of (1), (2) and (4).
8. A method for producing a density-controllable isotope carrier in accordance with claim 1, wherein the screen used in the swing granulator is 5 to 80 mesh.
9. The method for preparing a density-controllable isotope carrier according to claim 1, wherein the spheronization is carried out in a spheronizer at a spheronization rotation speed of 0 to 300 revolutions per minute and an air flow speed of 0 to 100m3 per hour for 1 to 20 minutes, and the binder or the solvent for the binder is added during the spheronization in an amount of 0 to 20% of the total material amount.
10. The method for preparing a density-controllable isotope carrier according to claim 1, wherein the drying process is carried out by using a fluidized drying machine, the drying temperature is 30 to 90 ℃, and the air flow rate is 0 to 1500m3/h for 0.1 to 3 hours.
CN202210565022.7A 2022-05-23 2022-05-23 Preparation method of density controllable isotope carrier Withdrawn CN114837656A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN202210565022.7A CN114837656A (en) 2022-05-23 2022-05-23 Preparation method of density controllable isotope carrier
CN202210883288.6A CN114991759B (en) 2022-05-23 2022-07-26 Density controllable isotope solid tracer carrier for oil field logging and its preparation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210565022.7A CN114837656A (en) 2022-05-23 2022-05-23 Preparation method of density controllable isotope carrier

Publications (1)

Publication Number Publication Date
CN114837656A true CN114837656A (en) 2022-08-02

Family

ID=82571397

Family Applications (2)

Application Number Title Priority Date Filing Date
CN202210565022.7A Withdrawn CN114837656A (en) 2022-05-23 2022-05-23 Preparation method of density controllable isotope carrier
CN202210883288.6A Active CN114991759B (en) 2022-05-23 2022-07-26 Density controllable isotope solid tracer carrier for oil field logging and its preparation method

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN202210883288.6A Active CN114991759B (en) 2022-05-23 2022-07-26 Density controllable isotope solid tracer carrier for oil field logging and its preparation method

Country Status (1)

Country Link
CN (2) CN114837656A (en)

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1220176A (en) * 1984-03-15 1987-04-07 George A. Burbidge High pressure well radioisotope injection system
US4994013A (en) * 1988-07-28 1991-02-19 Best Industries, Inc. Pellet for a radioactive seed
CN1055339C (en) * 1992-07-15 2000-08-09 中国核动力研究设计院 Survey of wells by radioactive isotope tracking method
US5591118A (en) * 1993-11-12 1997-01-07 Bierck; Barnes R. Low permeability waste containment construction and composition containing granular activated carbon and method of making
US6582819B2 (en) * 1998-07-22 2003-06-24 Borden Chemical, Inc. Low density composite proppant, filtration media, gravel packing media, and sports field media, and methods for making and using same
JP2003342872A (en) * 2002-05-29 2003-12-03 Rengo Co Ltd Functional material containing radioactive mineral and method for producing the same
US20120031613A1 (en) * 2005-08-09 2012-02-09 Momentive Specialty Chemicals Inc. Methods and compositions for determination of fracture geometry in subterranean formations
US9976070B2 (en) * 2010-07-19 2018-05-22 Baker Hughes, A Ge Company, Llc Method of using shaped compressed pellets in well treatment operations
JP5750312B2 (en) * 2011-06-06 2015-07-22 大日精化工業株式会社 Adsorbent composition, adsorbent and construction method thereof
CN102445389B (en) * 2011-09-22 2013-03-27 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
AU2012340949B2 (en) * 2011-11-22 2016-08-04 Baker Hughes Incorporated Method of using controlled release tracers
JP2013188716A (en) * 2012-03-14 2013-09-26 Mitsubishi Paper Mills Ltd Magnetic adsorbent
US9594070B2 (en) * 2013-11-05 2017-03-14 Spectrum Tracer Services, Llc Method using halogenated benzoic acid esters and aldehydes for hydraulic fracturing and for tracing petroleum production
JP6379382B2 (en) * 2014-03-20 2018-08-29 株式会社化研 Iodine removing agent, removing apparatus and removing method for removing iodine from aqueous solution
CN104043418A (en) * 2014-06-26 2014-09-17 青岛国航祥玉技术服务有限公司 Material for adsorbing cadmium-containing industrial wastewater
GB201503644D0 (en) * 2015-03-04 2015-04-15 Johnson Matthey Plc Tracer and method
JP6683821B2 (en) * 2015-11-07 2020-04-22 インテグリス・インコーポレーテッド Adsorbent and fluid supply package and apparatus containing same
CN106361708A (en) * 2016-09-30 2017-02-01 广州中大南沙科技创新产业园有限公司 High-density micropill core and preparation method thereof
US10752831B2 (en) * 2017-03-15 2020-08-25 Carbo Ceramics Inc. Catalytic proppant and methods for making and using same
US11154838B2 (en) * 2017-09-29 2021-10-26 Ingevity South Carolina, Llc Low emissions, high working capacity adsorbent and canister system
CN108315007A (en) * 2018-02-05 2018-07-24 河南省科学院同位素研究所有限责任公司 A kind of radioactive label fracturing propping agents and preparation method thereof that "dead" dust generates
CN108412487B (en) * 2018-03-07 2021-06-11 河南省科学院同位素研究所有限责任公司 High-pressure-resistant radioactive isotope tracer and preparation method thereof
EP3892368A4 (en) * 2018-12-05 2022-08-10 Ajinomoto Co., Inc. Sintered body for adsorption, production method therefor, and adsorption device
CN109880605B (en) * 2019-03-27 2020-04-14 中国石油化工股份有限公司 Curing agent sustained-release capsule and channeling-preventing agent for gas injection and channeling prevention and preparation method thereof
CN111905702A (en) * 2019-05-10 2020-11-10 核工业理化工程研究院 Preparation method of porous particle filter material loaded with nano zero-valent iron for adsorbing and removing heavy metals in water
CN110250565A (en) * 2019-06-10 2019-09-20 江西中烟工业有限责任公司 A kind of plant granule perfume (or spice) pearl and the preparation method and application thereof
CN110743487B (en) * 2019-10-30 2020-11-17 河北麦森钛白粉有限公司 Preparation method and application of adsorbing material for adsorbing radioactive elements
US10961444B1 (en) * 2019-11-01 2021-03-30 Baker Hughes Oilfield Operations Llc Method of using coated composites containing delayed release agent in a well treatment operation
RU2749223C1 (en) * 2020-03-27 2021-06-07 Общество с ограниченной ответственностью «ГеоСплит» Method of qualitative and quantitative estimation of downhole gas inflows in multistage hydraulic fracturing in a multiphase flow system
CN112177600A (en) * 2020-08-10 2021-01-05 浙江海洋大学 Oil leakage monitoring technology adopting radioactive tracer
CN114251088B (en) * 2021-12-22 2022-08-09 河南省科学院同位素研究所有限责任公司 Efficient zero-radioactive-emission well logging tracer and preparation method thereof
CN114382464B (en) * 2022-01-18 2022-09-02 河南省科学院同位素研究所有限责任公司 Method for screening radioactive isotope logging tracer agent underground
CN114382463B (en) * 2022-01-18 2022-08-19 河南省科学院同位素研究所有限责任公司 Radioactive isotope well logging tracer screening device in pit

Also Published As

Publication number Publication date
CN114991759B (en) 2023-09-08
CN114991759A (en) 2022-09-02

Similar Documents

Publication Publication Date Title
CN102485830A (en) Profile control oil-displacement agent for core-shell type inorganic/organic polymer composite microballoon
CN102617769A (en) Nanometer composite porous gel microsphere and preparation method thereof
CN102070152A (en) Functionalized homogeneous particle porous silicon dioxide microspheres and preparation method and application thereof
CN104226256A (en) Spherical forming Cu base metal organic skeleton-graphene oxide composite material and preparation method of spherical forming Cu base metal organic skeleton-graphene oxide composite material
CN114991759B (en) Density controllable isotope solid tracer carrier for oil field logging and its preparation method
CN107447292B (en) A kind of preparation method and applications of micro-nano spiral porous fibre
CN105435722A (en) Preparation method of hollow polylactic acid microcapsules consisting of poly(L-lactic acid) and poly(D-lactic acid)
CN105536352A (en) High-efficiency low-resistance staggered nano-fiber composite and preparation method thereof
CN109575906A (en) The polymer composite proppant particles and its preparation method of resin film cladding and application
CN108926881B (en) Device and method for separating two-dimensional nano material by continuous hypergravity percolation
CN112282722B (en) Low-density organic water-control proppant and preparation method thereof
CN108412487B (en) High-pressure-resistant radioactive isotope tracer and preparation method thereof
CN107617426A (en) A kind of preparation method of high adsorption capacity crystalline substance glue microsphere particle
CN109265710B (en) Cellulose microsphere with uniform size and preparation method thereof
CN106190091A (en) A kind of waterproofing type proppant of oil thoroughly and preparation method thereof
CN106861663A (en) A kind of micro-fluidic synthesis trace adsorbent for copper-containing wastewater treatment
CN108823670B (en) Diatomite fiber and preparation method thereof
CN113121293B (en) Preparation method of narrow-particle-size-distribution nano energetic composite microspheres based on membrane emulsification technology
CN1071591C (en) Tri-layer sphere type capsule breaker and preparing method thereof
CN111424321B (en) Fiber generating device capable of timely adsorbing ocean spilled oil
CN111762779B (en) Coal-based activated carbon, columnar activated carbon and preparation method thereof
CN114656816A (en) Novel water-based aerogel coating and preparation method thereof
CN107417968B (en) Surface modification method of heavy calcium carbonate and method for preparing high polymer composite material by adopting method
CN115059456B (en) Degradable radioisotope tracer and preparation method thereof
CN114904539B (en) Composite zein film and preparation method and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication

Application publication date: 20220802

WW01 Invention patent application withdrawn after publication