RING-SHAPED CATALYST FOR PREPARING ACROLEIN AND ACRYLIC ACID, AND USE THEREOF (As Amended)
US-2015367329-A1 · Dec 24, 2015 · US
US9440904B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9440904-B2 |
| Application number | US-201414903418-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 17, 2014 |
| Priority date | Jul 18, 2013 |
| Publication date | Sep 13, 2016 |
| Grant date | Sep 13, 2016 |
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Provided is a method capable of producing acrolein and/or acrylic acid, or methacrolein and/or methacrylic acid, stably in a high yield over a long period of time advantageously even in a high-load reaction, and the method is a method in which when preparing two or more kinds of catalysts having different formulations and stacking two or more layers in the axial direction of the tube, the catalysts are filled in such a manner that not only the component amount of bismuth relative to molybdenum decreases from the gas inlet side toward the gas outlet side, but also the component amount of iron relative to molybdenum increases from the gas inlet side toward the gas outlet side.
Opening claim text (preview).
The invention claimed is: 1. A method for producing an unsaturated aldehyde and/or an unsaturated carboxylic acid, the method comprising: subjecting an alkene to gas-phase catalytic partial oxidation with molecular oxygen by using a multitubular oxidation reactor having a complex metal oxide catalyst filled therein, thereby producing a corresponding unsaturated aldehyde and/or unsaturated carboxylic acid, wherein when preparing two or more kinds of catalysts having different formulations and stacking two or more layers in an axial direction of a tube, thereby achieving multilayer filling, the catalysts are filled in such a manner that not only a component amount of bismuth relative to molybdenum decreases from a gas inlet side toward a gas outlet side, but also a component amount of iron relative to molybdenum increases from the gas inlet side toward the gas outlet side. 2. The production method according to claim 1 , wherein the catalyst for producing an unsaturated aldehyde and/or an unsaturated carboxylic acid contains a compound represented by the following formula (1), the catalyst being prepared by a method in which in a step of preparing the compound represented by the following formula (1): a molybdenum component raw material is constituted of only an ammonium molybdate, and a weight of water for dissolution is 8.5 times or less relative to a weight of molybdenum contained in the ammonium molybdate; a bismuth component raw material is constituted of only bismuth nitrate, a weight of a nitric acid aqueous solution for dissolution is 2.3 times or more relative to a weight of bismuth contained in the bismuth nitrate, and a concentration of nitric acid of the nitric acid aqueous solution for dissolving bismuth nitrate therein is 10% by weight or more, and is filled in at least one layer on the most gas outlet side in the tube axis: MO 12 Bi a Fe b CO c Ni d X e Y f Z g O h Formula (1) wherein X is at least one element selected from the group consisting of magnesium (Mg), calcium (Ca), manganese (Mn), copper (Cu), zinc (Zn), cerium (Ce) and samarium (Sm); Y is at least one element selected from the group consisting of boron (B), phosphorus (P), arsenic (As), antimony (Sb) and tungsten (W); Z is at least one element selected from the group consisting of sodium (Na), potassium (K), rubidium (Rb) and cesium (Cs); a to g represent atomic ratios of the respective components; h is a numerical value determined by degrees of oxidations of the catalyst components; a=0.80 to 2.0; b=1 to 2.5; c=3 to 7; d=2 to 3.5; e=0 to 10; f=0 to 10; g=0.01 to 0.10; h is expressed by the numerical value satisfying the oxidation states of other elements; d/a is 1.9 or more and 3.2 or less; d/g is 29 or more and 69 or less; and a/g is 18 or more and 35 or less. 3. The production method according to claim 1 , wherein a form of the complex metal oxide catalyst is a spherical coating catalyst in which catalytic active components are supported on a surface of an inert carrier. 4. The production method according to claim 1 , wherein a load of the alkene in raw material gas to be supplied into the multitubular oxidation reactor is 120 times or more (converted in a standard state) relative to a unit catalyst volume per one hour. 5. The production method according to claim 1 , wherein a load of the alkene in raw material gas to be supplied into the multitubular oxidation reactor is 140 times or more (converted in a standard state) relative to a unit catalyst volume per one hour. 6. The production method according to claim 1 , wherein a load of the alkene in raw material gas to be supplied into the multitubular oxidation reactor is 160 times or more (converted in a standard state) relative to a unit catalyst volume per one hour. 7. The production method according to claim 1 , wherein a concentration of the alkene contained in raw material gas to be supplied into the multitubular oxidation reactor is 7.5% by volume or less. 8. The production method according to claim 1 , wherein the catalysts filled in all of the layers of the multitubular oxidation reactor are in a non-diluted state where dilution with an inert substance by physical mixing is not made. 9. A method for producing acrolein and/or acrylic acid, or methacrolein and/or methacrylic acid, by the production method according to claim 1 .
Constitutive chemical elements of heterogeneous catalysts · CPC title
Granulating · CPC title
Mixed oxides other than spinels, e.g. perovskite · CPC title
in propene or isobutene · CPC title
of propene, butenes, acrolein or methacrolein · CPC title
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