Vanadium oxide powder with high latent heat of phase change and preparation method thereof
A technology of latent heat of phase change and vanadium oxide, applied in the direction of vanadium oxide, chemical instruments and methods, heat exchange materials, etc., can solve the problems of poor phase change performance of products, achieve low cost, facilitate mass production, and low price Effect
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Embodiment 1
[0069] Get 0.335g vanadium pentoxide and 0.249g anhydrous oxalic acid, add 35ml deionized water, stir at room temperature for 1 hour, then add 0.013g polyvinylpyrrolidone (PVP) and stir for 15 minutes to obtain PVP, vanadium pentoxide and oxalic acid Uniform precursor dispersions with mass concentrations of 0.037%, 0.94% and 0.70%, respectively. The dispersion liquid was added to a 100ml p-polyphenol (PPL) liner, and then the liner was placed in a reaction kettle, and then hydrothermally reacted at 220° C. for 8 hours. After the hydrothermal reaction was completed, it was cooled to room temperature. After the reaction suspension was centrifuged and washed in a high-speed centrifuge. The obtained product was then dried in an oven at 50°C for 20 hours to obtain PVP-modified nano-VO 2 (B) powder (denoted as VO 2 (B)-PVP-1).
[0070] Weigh 0.2g of VO prepared above 2 (B) The powder is placed in a tube furnace, and the powder is degassed for 80 minutes in a low vacuum with an ...
Embodiment 2
[0077] Get 0.364g vanadium pentoxide and 0.378g oxalic acid dihydrate, add 40ml deionized water, stir at room temperature for 2 hours, then add 0.017g polyvinylpyrrolidone (PVP) and stir for 10 minutes to obtain PVP, vanadium pentoxide and oxalic acid Uniform precursor dispersions with mass concentrations of 0.042%, 0.89% and 0.66%, respectively. The dispersion liquid was added to a 100ml p-polyphenol (PPL) liner, and then the liner was placed in a reaction kettle, and then hydrothermally reacted at 240° C. for 4 hours. After the hydrothermal reaction was completed, it was cooled to room temperature. After the reaction suspension was centrifuged and washed in a high-speed centrifuge. The obtained product was then dried in an oven at 80°C for 12 hours to obtain PVP-modified nano-VO 2 (B) powder (denoted as VO 2 (B)-PVP-2).
[0078] Weigh 0.2g of VO prepared above 2 (B) The powder is placed in a tube furnace, and the powder is degassed for 30 minutes in a low vacuum with an...
Embodiment 3
[0084] Get 0.345g vanadium pentoxide and 0.359g dihydrate oxalic acid, add 45ml deionized water, stir at room temperature for 3 hours, then add 0.022g polyvinylpyrrolidone (PVP) and stir for 15 minutes to obtain PVP, vanadium pentoxide and oxalic acid Uniform precursor dispersions with mass concentrations of 0.048%, 0.75% and 0.56%, respectively. The dispersion liquid was added to a 100ml p-polyphenol (PPL) lining, and then the lining was placed in a reaction kettle, and then hydrothermally reacted at 230°C for 6h. After the hydrothermal reaction was completed, it was cooled to room temperature. After the reaction suspension was centrifuged and washed in a high-speed centrifuge. The resulting product was then dried in an oven at 70°C for 16 hours to obtain PVP-modified nano-VO 2 (B) powder (denoted as VO 2 (B)-PVP-3).
[0085] Weigh 0.2g of VO prepared above 2 (B) The powder is placed in a tube furnace, and the powder is degassed for 80 minutes in a low vacuum with an air...
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