Chlorine-containing organic matter combustion catalyst with high HCl selectivity and preparation method thereof
A combustion catalyst, selective technology, applied in combustion methods, physical/chemical process catalysts, chemical instruments and methods, etc., to inhibit the formation of polychlorinated products and avoid secondary pollutants.
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Embodiment 1
[0014] Weigh 2.53g of ammonium metavanadate, dissolve it in ethanolamine aqueous solution, heat to dissolve; weigh 10gTiO 2 , mixed it into a ball mill jar, ball milled it at 500 rpm for 30 minutes, then coated it on the surface of the monolithic honeycomb ceramics, and dried it overnight at 100°C; then, fired it at 600°C for 4 hours to prepare Obtain A; then, impregnate Ru solution on the surface of A, dry at 100°C for 20 hours; bake at 500°C for 4 hours to obtain oxidation state catalyst B; pass oxidation state catalyst B through 10% H 2 -90%N 2 Under the atmosphere, reduce at 450°C for 2 hours to obtain the finished catalyst 0.01%Ru / 3%V-27%TiO 2 / whole honeycomb.
Embodiment 2
[0016] 10gTiO 2 , add 15g of water, make a slurry by ball milling, apply it on the surface of the whole honeycomb, dry it at 120°C, and dry it overnight; bake it at 550°C for 4 hours to make A; then impregnate the surface of A with a mixture of Ru and chromium nitrate Precursor salt solution, dried at 100°C for 20 hours; roasted at 500°C for 4 hours to obtain catalyst B in oxidation state; reduced catalyst B in oxidation state in hydrazine hydrate solution to obtain finished catalyst 0.01% Ru-10 %Cr / 20%TiO 2 / whole honeycomb.
Embodiment 3
[0018] Add 10g of CeZrOx and 15g of water, and make a slurry by ball milling, apply it on the surface of the whole honeycomb, and dry it at 140°C for 10 hours; at 700°C, bake it for 3 hours to prepare A; then, Immerse the precursor salt solution of ammonium metavanadate and chromium nitrate on the surface of A, dry at 100°C for 10 hours; bake at 500°C for 4 hours to prepare B; then impregnate the Ru precursor solution on the surface of B, Dry at 80°C for 24 hours; roast at 500°C for 3 hours to obtain catalyst C in oxidation state; pass catalyst C in oxidation state through 10% H 2 -90%N 2 Reduction, the finished catalyst is prepared 0.02%Ru / 5%V-5%Cr / 25%CeZrOx / integral honeycomb.
[0019] Catalyst evaluation conditions:
[0020] Activity evaluation conditions: 1000ppm chlorobenzene, air as balance gas, GHSV=20000h -1 , the loading amount of the catalyst is 1ml, and the results are shown in the table below.
[0021] The following table compares the performance of different c...
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