Catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone and its preparation method and application

A technology of methyl isobutyl ketone and diisobutyl ketone is applied to the catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone and the field of preparation thereof, and can solve the problems of poor catalyst activity and high cost, Achieve the effect of enhancing corporate profitability, strong adaptability, and promoting even distribution

Active Publication Date: 2022-03-29
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] In order to solve the problems of poor catalyst activity and high cost in the prior art, the present invention proposes a catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone

Method used

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  • Catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone and its preparation method and application
  • Catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone and its preparation method and application

Examples

Experimental program
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Effect test

Embodiment 1

[0036] The 10ml hydrochloric acid solution that contains 7.44g bismuth chloride is mixed with the 100ml aqueous solution that contains 150g calcium nitrate to make solution I, takes by weighing 40.25g diammonium hydrogen phosphate and is dissolved in water and makes concentration be the solution II of 0.12mol / L, will Solution II was slowly added dropwise to solution I, the Ca / P molar ratio was 3, and at the same time, 0.05mol / L aqueous urea solution was added dropwise to adjust the pH value to 8.5, and stirred at 40°C for 5h to obtain slurry III; weigh 19.6 Add 24.4g nickel nitrate and 24.42g cobalt nitrate to the slurry III, and add dropwise 0.05mol / L urea aqueous solution to adjust the pH value of the solution, control the pH value of the precipitation end point to 7.0, and age the prepared slurry IV at 50°C for 10h , and then filtered and washed to obtain a wet filter cake; the filter cake was dried at 120°C for 2 hours, decomposed at 450°C, and hydrogen was introduced at a ...

Embodiment 2

[0038] The 10ml hydrochloric acid solution that contains 3.38g bismuth chloride is mixed with the 100ml aqueous solution that contains 140g calcium nitrate to make solution I, takes by weighing 32.2g diammonium hydrogen phosphate and is dissolved in water and makes concentration be the solution II of 0.10mol / L, will Solution II was slowly added dropwise to solution I, the Ca / P molar ratio was 3.5, and at the same time, 0.05mol / L aqueous urea solution was added dropwise to adjust the pH value to 9.0, and stirred at 60°C for 5h to obtain slurry III; weigh 21.7 Add 2 g of nickel sulfate and 20.03 g of cobalt nitrate to the slurry III, and add 0.05 mol / L aqueous urea solution dropwise to adjust the pH value of the solution, and control the pH value of the precipitation end point to 7.5, and age the prepared slurry IV at 90°C for 5 h , and then filtered and washed to obtain a wet filter cake; the filter cake was dried at 120°C for 2 hours, decomposed at 400°C, and hydrogen was intro...

Embodiment 3

[0040] The 10ml hydrochloric acid solution that contains 5.41g bismuth chloride is mixed with the 100ml aqueous solution that contains 140g calcium nitrate to make solution I, takes by weighing 97.35g dipotassium hydrogen phosphate and is dissolved in water and makes concentration be the solution II of 0.1mol / L, will Solution II was slowly added dropwise to solution I, the Ca / P molar ratio was 2.0, and at the same time, 0.05mol / L aqueous urea solution was added dropwise to adjust the pH value to 10.0, and stirred at 70°C for 4h to obtain slurry III; weigh 19.6 Add 2 g nickel nitrate and 24.42 g cobalt nitrate to slurry III, and add 0.05 mol / L aqueous urea solution dropwise to adjust the pH value of the solution, control the pH value of the precipitation end point to 8.5, and age the prepared slurry IV at 100 ° C for 3 h , and then filtered and washed to obtain a wet filter cake; the filter cake was dried at 120°C for 2 hours, decomposed at 320°C, and hydrogen was introduced at ...

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Abstract

The invention relates to a catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone, a preparation method and application thereof in the field of catalysts. The catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone is measured as 100 parts by the overall weight of the catalyst, and includes the following components: a, 0.5 to 10 parts of at least One; b, 0.5-10 parts of at least one selected from cobalt or cobalt oxides; c, 80-99 parts selected from bismuth-modified basic calcium phosphate. The preparation process of the catalyst of the present invention is relatively simple, easy to control, and the active components should not be lost; the catalyst of the present invention can not only produce methyl isobutyl ketone, but also diisobutyl ketone, and the industrial production device has better adaptability to the market. Strong, the cost of the bimetallic catalyst of the present invention is significantly lower than that of the existing palladium catalyst, and has better economic benefits.

Description

technical field [0001] The invention relates to the field of catalysts, in particular to a catalyst for synthesizing methyl isobutyl ketone and diisobutyl ketone from acetone, a preparation method and application thereof. Background technique [0002] Methyl isobutyl ketone, also known as 4-methyl-2-pentanone (abbreviated as MIBK in English), is an important solvent and chemical intermediate. It has attracted much attention because of its excellent performance. The color is transparent, the boiling point belongs to the middle boiling point, the solubility is very strong, and it can be miscible with many organic solvents such as alcohol, benzene, ether, etc. It can be used as paint, ethyl cellulose, nitrocellulose, audio and video tapes, paraffin, various natural or synthetic Raw materials for resin solvents, dewaxing agents, rare earth metal extractants, polymerization initiators, surfactants, medicines, pesticide extractants, and rubber antioxidants are currently relatively...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/186B01J37/03C07C45/73C07C49/04
Inventor 唐国旗田保亮李宝芹
Owner CHINA PETROLEUM & CHEM CORP
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