Nanoparticle for inhibiting or eliminating heavy oil asphaltene deposition and preparation method thereof
A nanoparticle and asphaltene technology, applied in the preparation of test samples, chemical instruments and methods, and drilling compositions, to achieve efficient dissolution and improve thermal performance
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Embodiment 1
[0028] A nanoparticle for inhibiting or removing heavy oil asphaltene deposition, the nanoparticle is nano Ni 2 O, nano Fe 2 o 3 , Nano Fe 3 o 4 , Nanometer sodium iron silicate (NaFeSi 2 o 6 ), nano-MoO 3 、Co 3 o 4 , Nano WO 3 , Nano Al 2 o 3 , Nano ZrO 2 , Nano ZnO, Nano CuO, Nano TiO 2 , nano-SiO 2 1. One or more nanoparticle mixtures of amine-modified carpapite nanoparticles, modified fly ash nanoparticles, and modified apatite nanoparticles.
Embodiment 2
[0030] A kind of nano Ni 2 The preparation method of O particles is to prepare NiO nanoparticles in situ. Add 2.5ml of 4M nickel (II) nitrate aqueous solution to 50ml of oil matrix, and use a vortex mixer to vigorously mix the sample for 5 minutes. After mixing, no phase separation occurs. The oil matrix can be considered as a single phase, then the sample is introduced into the reactor unit, heat treated at 300°C for 12 hours in a sealed reactor unit, the control sample of the same composition only lacks the precursor salt, the same heat treatment is required to account for the heat treatment due to the Any resulting precipitation of asphaltenes; the particles were recovered by centrifuging the oil matrix at 5000 rpm for 20 minutes, the upper phase was decanted and collected and the lower phase was washed several times with toluene until a clear toluene phase was obtained, centrifugation of the control samples was observed not to result in any precipitation.
Embodiment 3
[0032] 10000 ppm hyperdispersed Fe in the oil phase was prepared by slowly adding and mixing 2 ml volume of 4 M iron(III) nitrate nonahydrate aqueous solution into the 50 ml oil phase 2 o 3 Nanoparticles, other concentrations of nanoparticles were prepared in situ by keeping the volume of the water-soluble precursor at a fixed value, then reducing the concentration of nanoparticles, mixing the oil matrix vigorously using a vortex mixer until no phase separation could be observed, and the oil The matrix was considered as a single phase; the sample was transferred to a 100 ml Parr reactor unit (PARR Instrument Company, USA), and after mixing at 160 °C in a sealed unit, it was heat treated at 200 °C for 4 hours; in order to account for the pitch Mass deposition, a control sample with the same composition, only the precursor salts were removed, and the same heat treatment was performed; particle recovery from the oil phase was accomplished by centrifuging the oil phase at 5000 rpm...
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