Improved air purification system and method for removing formaldehyde
US-2017291164-A1 · Oct 12, 2017 · US
US9266094B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9266094-B2 |
| Application number | US-201214240056-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 29, 2012 |
| Priority date | Aug 31, 2011 |
| Publication date | Feb 23, 2016 |
| Grant date | Feb 23, 2016 |
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The present invention relates to a catalyst comprising a ceramic support with a BET surface area of less than 40 m 2 /g and (a) 1.0 to 100 g of at least one metal of groups 8 to 12 of the periodic table of the elements, (b) 1.0 g to 100 g of at least one metal of groups 4 to 6 and 12 of the periodic table of the elements and (c) 1.0 g to 100 g of at least one metal of groups 14 and 15 of the periodic table of the elements per liter of bulk volume of the ceramic support, wherein the catalyst is additionally doped with (d) potassium in a content of from 0.0050% by weight to 0.20% by weight, based on the total weight of the catalyst. The present invention also provides the use of such a catalyst in the catalytic gas phase hydrogenation of nitroaromatics.
Opening claim text (preview).
The invention claimed is: 1. A catalyst comprising an α-aluminium oxide ceramic support with a BET surface area of less than 10 m 2 /g and (a) 8.0 g to 50 g of palladium, (b) 8.0 g to 50 g of vanadium and (c) 2.0 g to 10 g of lead, per liter of bulk volume of the α-aluminium oxide, wherein the catalyst is doped with (d) potassium in a content of from 0.070% by weight to 0.12% by weight, based on the total weight of the catalyst. 2. The catalyst according to claim 1 , in which the catalyst is doped with potassium (d) in the form of potassium sulfate, potassium chloride, potassium hydroxide, potassium carbonate, potassium bicarbonate, potassium bromide; potassium acetate, potassium formate and/or potassium nitrate. 3. The catalyst according to claim 2 , in which the catalyst is doped with potassium (d) in the form of potassium sulfate or potassium chloride. 4. A process for the preparation of aromatic amines of the formula in which R1 and R2 independently of each other denote hydrogen, methyl or ethyl, wherein R1 can additionally denote NH 2 , by hydrogenation of nitroaromatics of the formula in which R2 and R3 independently of each other denote hydrogen, methyl or ethyl, wherein R3 can additionally denote NO 2 , with hydrogen in the presence of the catalyst according to claim 1 . 5. The process according to claim 4 , in which aniline is prepared by hydrogenation of nitrobenzene. 6. The process according to claim 4 , in which the hydrogenation is carried out isothermally in a reactor with removal of the resulting heat of reaction by a cooling medium. 7. The process according to claim 4 , in which the molar ratio of hydrogen to nitro groups is 3 to 30:1, the absolute pressure at the entry of the reactor is 0.500 bar to 6.00 bar, the entry temperature of the gaseous reaction mixture is 200° C. to 460° C., and the maximum catalyst temperatures are 600° C.
with gases containing free hydrogen · CPC title
Constitutive chemical elements of heterogeneous catalysts · CPC title
Pretreatment of the support · CPC title
Chlorides · CPC title
by reduction of nitro groups bound to carbon atoms of six-membered aromatic rings {in presence of hydrogen-containing gases and a catalyst} · CPC title
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