Titanium oxide coating/foam silicon carbide structure catalytic carrier and preparation method thereof
A technology of silicon carbide foam and catalytic carrier, which is applied in the direction of catalyst carrier, chemical instrument and method, physical/chemical process catalyst, etc., can solve the problems of unfavorable titanium oxide catalytic performance, catalyst wear, complicated operation, etc., and achieve unique catalytic performance, Efficiency improvement, absorption efficiency improvement effect
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Embodiment 1
[0032] In this embodiment, the preparation process of the silicon carbide foam ceramic structure catalyst carrier with nano-titanium oxide coating is as follows:
[0033] 1. Prepare a slurry with a weight ratio of silicon carbide micropowder (average particle size 10nm): epoxy resin: iron micropowder: dehydrated alcohol=100:50:0.75:50, and ball mill it for 2 hours before use.
[0034] 2. Immerse the polyurethane foam in the above slurry for 2 minutes, blow off the excess slurry with compressed air after taking it out, dry it at 150°C and weigh it. Repeat the above process until the required weight (0.95 g / ml) is reached to obtain a foamed silicon carbide precursor.
[0035] 3. The foamed silicon carbide precursor obtained in step 2 was pyrolyzed at 800°C for 0.5 hours under the protection of argon. After pyrolysis, the sample was sintered at 1600°C for 1 hour under a silicon atmosphere to obtain foamed silicon carbide with P-type semiconductor characteristics. Foamed silicon ...
Embodiment 2
[0042]1. Slurry is prepared in the ratio of silicon carbide micropowder (average particle size 10 μm) by weight: phenolic resin: iron element in iron oxide micropowder: dehydrated alcohol=100:120:2:80, and it is standby after ball milling for 2 hours.
[0043] 2. Immerse the polyurethane foam in the above slurry for 5 minutes, blow off the excess slurry with compressed air after taking it out, dry it at 50°C, dip it again and dry it, and repeat it several times until the dried sample meets the requirements. The weight (1 g / mL) to obtain a foamed silicon carbide precursor.
[0044] 3. The foamed silicon carbide precursor obtained in step 2 was pyrolyzed at 1200°C for 0.5 hours under the protection of nitrogen. After pyrolysis, the sample was sintered at 1700°C for 2 hours under a silicon atmosphere to obtain foamed silicon carbide with P-type semiconductor characteristics. The foam Silicon carbide was treated in 4M sodium hydroxide solution at 100°C for 10 minutes to increase t...
Embodiment 3
[0051] The difference from Example 1 is:
[0052] The slurry was prepared in the ratio of silicon carbide micropowder (average particle size 50nm):furfural resin:nickel micropowder:absolute ethanol=100:50:0.75:50 by weight, and ball milled for 2 hours before use.
[0053] After the polyurethane foam was dipped in the above slurry and dried several times, the dried sample reached the required weight (1.35 g / ml), and a foamed silicon carbide precursor was obtained.
[0054] A suspension was prepared at a weight ratio of titania sol: titania microparticles: nitrogen element in ammonium chloride = 100:15:7.5, and ball milled for 1 hour to obtain coating slurry.
[0055] After soaking the foamed silicon carbide in the coating slurry and drying it for several times, the coating load reached the required weight (0.15 g / ml).
[0056] In this embodiment, the weight content of the titanium oxide coating is 10%, and the rest is a foamed silicon carbide matrix. The fracture micrograph o...
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