Shale pore structure fluid flow channel tracer, preparation method and tracing method
A pore structure and fluid flow technology, which is applied in the field of shale pore structure fluid flow channel tracer, preparation of shale micro-nano pore fluid flow channel tracer, and shale pore structure fluid flow channel tracer field , which can solve the problem that it is difficult to directly obtain the fluid migration information in the micro-nano pores of shale, and achieve the effect of high resolution, obvious tracer and simple steps.
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[0064] The preparation method of above-mentioned gold nano particle tracer, it specifically comprises the following steps:
[0065] S1) Uniformly disperse 0.4 g of polyvinylpyrrolidone in ultrapure water.
[0066] S2) Add an aqueous solution of chloroauric acid and a reducing agent to the dispersion in step S1).
[0067] Described chloroauric acid solution concentration is 2.44 * 10 -3 mol / L~5.0×10 -3 mol / L; the reducing agent is preferably trisodium citrate, or hydroxylamine hydrochloride or trisodium citrate and hydroxylamine hydrochloride.
[0068] S3) Heating the reaction liquid in step S2) to 75° C. and stirring for 30-60 min, the reaction is complete.
[0069] S4) Cool the system after complete reaction to room temperature, disperse in ultrapure water added with polyethylene glycol, and stir for 1-2 hours to obtain gold nanoparticles.
[0070] The preparation method of above-mentioned gold / ferric oxide composite nano particle tracer, it specifically comprises the fol...
Embodiment 1
[0091] In a 250mL flask, mix 0.4g polyvinylpyrrolidone and 80mL ultrapure water, then add 2.44×10 - 3 mol / L chloroauric acid solution 10ml, and the flask was placed in a constant temperature water bath and heated to 75°C, and then 3.43×10 -2 mol / L sodium citrate solution 3ml, continue to stir for 30min, after returning to room temperature, add 5mg of polyethylene glycol under stirring, continue stirring for 1h, to obtain gold nano tracer.
Embodiment 2
[0093] Weigh 2.34gFeCl 3 ·6H 2 O (ferric chloride hexahydrate) with 0.96g FeCl 2 4H 2 O (ferrous chloride tetrahydrate) was added to a flask (250 mL), and 100 mL of deoxygenated ultrapure water was added, and the flask was placed in a constant temperature water bath at 80° C., and nitrogen was filled in the flask to remove oxygen. Under mechanical stirring (stirring rate 800r / min), use a dropping funnel to slowly drop 40mL of NaOH solution with a concentration of 1.15mol / L into the flask. After the addition is complete, add 40mL of trisodium citrate with a concentration of 0.1mol / L , continue to react for 30min. After cooling to room temperature, the obtained particles were subjected to magnetic separation with a magnet, and washed three times with deoxygenated ultrapure water to obtain ferric oxide nanoparticles.
[0094] Take 50 mg of the prepared iron ferric oxide nanoparticles and put them into a beaker, add 150 mL of deoxygenated ultrapure water, and ultrasonicate for...
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