Light absorbing material and preparation method thereof
A light-absorbing material and ultraviolet light technology, applied in chemical instruments and methods, vanadium oxide, metal/metal oxide/metal hydroxide catalysts, etc. Complicated methods and other issues, to achieve the effects of wide and cheap raw material sources, degradation of air pollutants, and enhanced catalytic efficiency
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[0044] The preparation method of the light absorbing material of the present invention comprises the following steps:
[0045]1) Mixing materials: mix the oxalic acid solution and the vanadium-containing precursor, and fully stir to obtain a sol; wherein, the molar ratio of the vanadium in the vanadium-containing precursor to the carbon in the oxalic acid is 1: (1.5~3.5); The vanadium precursor includes any one of vanadium pentoxide and ammonium metavanadate;
[0046] 2) Hydrothermal reaction: react the sol obtained in step 1) at 220-250°C for 24-72 hours to obtain a crude product;
[0047] 3) Post-reaction treatment: washing and drying the crude product to obtain a light-absorbing material.
[0048] The inventive method, according to preset V:C mol ratio, in oxalic acid (H 2 C 2 o 4 ) into the deionized aqueous solution containing vanadium, and the sol was obtained after stirring evenly, and the sol was transferred to a hydrothermal kettle for hydrothermal reaction to obt...
Embodiment 1
[0060] (1) Preparation of sol: get 30mmol of H 2 C 2 o 4 Add it to 80mL of deionized water, stir evenly until completely dissolved; then take 10mmol of V 2 o 5 Dissolve in the above solution and stir evenly until completely dissolved to obtain a sol.
[0061] (2) Hydrothermal reaction: Clean the liner of the hydrothermal reaction kettle with deionized water and absolute ethanol, pour the sol prepared in step 1) into a 100mL liner of the hydrothermal reaction kettle, and react at 240°C for 48 hours, after cooling to room temperature, the product was alternately washed 3 times with water and absolute ethanol, and dried in an oven at 100°C for 10 hours to obtain the black product VO x Powder light absorbing material.
[0062] VO prepared in this embodiment x The powder scanning electron microscope picture is as follows figure 1 As shown, the morphology of the sample is similar to that of a spherical structure. The XRD pattern of the sample is as follows figure 2 As show...
Embodiment 2
[0064] (1) Preparation of sol: get 30mmol of H 2 C 2 o 4 Add to 80mL of deionized water, stir evenly until completely dissolved; then take 20mmol of NH 4 VO 3 Dissolve in the above solution and stir evenly until completely dissolved to obtain a sol.
[0065] (2) Hydrothermal reaction: Clean the liner of the hydrothermal reaction kettle with deionized water and absolute ethanol, pour the sol prepared in step 1) into a 100mL liner of the hydrothermal reaction kettle, and react at 240°C for 48 hours, after cooling to room temperature, the product was alternately washed 3 times with water and absolute ethanol, and dried in an oven at 150°C for 6 hours to obtain the black product VO x Powder light absorbing material.
[0066] The VO x The XRD pattern of the powder is shown in Figure 7 , similar to figure 2 , shown as the novel VO of the present invention x Crystal structure. Its reflection spectrum see Figure 8 , which proves that it has very strong absorption in ultr...
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