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Composite metal oxide catalyst and preparation method thereof

A composite oxide and composite metal technology, which is applied in the field of preparation of the composite metal oxide catalyst, can solve the problems of loss of active components, difficulty in accurately controlling the catalyst, uneven distribution of catalyst active components, etc.

Pending Publication Date: 2018-08-21
SHANGHAI HUAYI NEW MATERIAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, for different metal ions, the pH values ​​required for precipitation are different, so the order of metal ion precipitation during preparation is different, which will lead to uneven distribution of the prepared catalyst active components
In addition, if ammonia water is used as the precipitant, metal ions such as cobalt and nickel will form soluble complexes with the ions in the precipitant, resulting in the loss of active components, and it is difficult to accurately control the composition of the final catalyst.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0042] Therefore, the preparation method of the present invention includes: prefabricating a part of the composite oxide of molybdenum-bismuth two elements, and then preparing the remaining composite oxide (the remaining composite oxide may optionally contain molybdenum and bismuth elements in the remainder part) , the pre-made molybdenum-bismuth composite oxide was added in a stoichiometric amount.

[0043] In an example of the present invention, based on the respective total moles of molybdenum and bismuth elements, in the pre-prepared molybdenum-bismuth two-element composite oxide, the amount of each element accounts for 40-100% of the total amount respectively, It is preferably 50-98%, more preferably 60-95%, preferably 70-93%, most preferably 80-90%, preferably 85-88%.

[0044] The molybdenum-bismuth composite oxide catalyst finally prepared by the above method has the required molybdenum-bismuth composite oxide structure, so that the final composite oxide catalyst has th...

Embodiment 1

[0101] (i) Preparation of catalyst

[0102] Weigh 15.9 g of ammonium heptamolybdate and dissolve it in 50 mL of distilled water. Then weigh 29.1 grams of bismuth nitrate, dissolve it in 100 mL of distilled water and add a few drops of nitric acid to promote the dissolution of bismuth nitrate. While stirring, the bismuth nitrate solution was slowly added to the ammonium heptamolybdate solution, and ammonia water (concentration about 7 mol / L) was added dropwise at the same time to control the final value of the solution to 1.0. After the dropwise addition, the slurry was aged at 60° C. with stirring for 1 hour, then suction-filtered, and washed with distilled water until the filtrate was neutral.

[0103] Dry the filter cake in an oven at 110°C for 8 hours, and then roast it in an air atmosphere for 5 hours at a roasting temperature of 550°C to obtain a solid substance whose crystal phase is α-bismuth molybdate, and crush it into a powder with a particle size of less than 200 m...

Embodiment 2

[0110] (i) Preparation of catalyst

[0111] Weigh 10.6 g of ammonium heptamolybdate and dissolve it in 30 mL of distilled water. Then weigh 29.1 grams of bismuth nitrate, dissolve it in 100 mL of distilled water and add a few drops of nitric acid to promote the dissolution of bismuth nitrate. While stirring, the bismuth nitrate solution was slowly added to the ammonium heptamolybdate solution, and ammonia water (concentration about 7 mol / L) was added dropwise at the same time to control the final value of the solution to 1.0. After the dropwise addition, the slurry was aged at 60° C. with stirring for 1 hour, then suction-filtered, and washed with distilled water until the filtrate was neutral.

[0112] Dry the filter cake in an oven at 110°C for 8 hours, and then roast it in an air atmosphere for 5 hours at a roasting temperature of 600°C to obtain a solid substance whose crystal phase is β-bismuth molybdate, and crush it into a powder with a particle size of less than 200 m...

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Abstract

The invention discloses a composite metal oxide catalyst and a preparation method thereof, wherein the composite metal oxide catalyst has the following general formula, M is one or a variety of materials selected from V, Cr, Mn, Fe, Co and Ni, N is one or a variety of materials selected from Na, K, Cs, Ca and Ba, a is 1-20, b is 0.05-10, x is 1-20, y is 0.01-5, and z is the number meeting the valence states of each atom. The preparation method comprises: dissolving a Mo precursor compound and a Bi precursor compound, controlling the pH value of the slurry at 0.1-7.0, filtering, and calcining to obtain molybdenum-bismuth oxide solid particles; providing elements M and N and optionally the slurry of the Mo precursor compound and the Bi precursor compound; and dispersing the molybdenum-bismuth oxide solid particles into the slurry, and calcining to obtain the catalyst. The general formula is MoaBibMxNyOz.

Description

technical field [0001] The invention relates to a composite metal oxide catalyst, which is used for catalytic oxidation reactions such as the preparation of acrolein from propylene, the preparation of methacrolein from isobutene or tert-butanol, and the preparation of butadiene by oxidative dehydrogenation of butene. The catalyst of the invention has good low-temperature catalytic activity and selectivity to target products. The invention also relates to a preparation method of the composite metal oxide catalyst. Background technique [0002] Acrylic acid and methacrylic acid are important organic chemical products, which are mainly prepared industrially from propylene or isobutene (or tert-butanol) through a two-step catalytic oxidation method, that is, propylene or isobutene (or tert-butanol) in the Mo-Bi system Acrolein and methacrolein are partially oxidized under the action of a composite oxide catalyst, and the resulting aldehydes are further oxidized to form acrylic ...

Claims

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Application Information

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IPC IPC(8): B01J23/887C07C5/333C07C45/35C07C45/37C07C47/22C07C11/167
CPCB01J23/002B01J23/8876B01J2523/00C07C5/3332C07C45/35C07C45/37B01J2523/13B01J2523/54B01J2523/68B01J2523/842B01J2523/845B01J2523/12B01J2523/15C07C47/22C07C11/167
Inventor 翟夫鹏李雪梅庄岩马建学
Owner SHANGHAI HUAYI NEW MATERIAL