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Hydrogenation catalyst and preparation method and application thereof

A hydrogenation catalyst and catalyst technology, applied in the field of catalysis, can solve the problems of easy pulverization of the catalyst, poor selectivity, and low product quality, and achieve the effects of smooth catalyst pores, high mechanical stability, and strong conversion ability.

Active Publication Date: 2020-09-29
WANHUA CHEM GRP CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] CN1260193C discloses a method for decomposing ammonium formate in a reaction mixture containing polyhydric alcohols. The hydrogenation liquid decomposes ammonium formate by heating up in another reactor under the action of a catalyst such as Co / Cu / Ni. The reaction temperature is as high as 180° C., increasing Reduced equipment investment and operating costs
[0013] At present, when the catalyst prepared by the prior art is used for the hydrogenation of 2,2-dimethylolbutyraldehyde to prepare trimethylolpropane, there is insufficient hydrogenation ability of 2,2-dimethylolbutyraldehyde, 2,2 -Dimethylolbutyraldehyde is easy to decompose on the catalyst, resulting in poor selectivity, poor formate conversion ability of the catalyst, resulting in low product quality, and easy pulverization of the catalyst, etc.

Method used

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  • Hydrogenation catalyst and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0079] (1) Add 300g water, 3.0g dimethyl dodecyl [3-(trimethoxysilyl) propyl group] ammonium chloride and 9g hydroxymethyl cellulose in the reaction kettle and stir evenly to obtain dispersion liquid I .

[0080] (2) 273.4g copper nitrate (Cu(NO 3 ) 2 ·3H 2 O, 242), 167.1g zinc nitrate (Zn(NO 3 ) 2 ·6H 2 O, 298) and 163.4g aluminum nitrate (Al(NO 3 ) 3 9H 2 (2,375) was dissolved in 1471g water to prepare mixed salt solution, and preparation concentration was 15wt% sodium carbonate aqueous solution, and above-mentioned two kinds of solutions were heated to 60 ℃ respectively and then co-flow was added dropwise in the aforementioned reactor, and the time of dropping was 40min. The temperature of the precipitation process was controlled at 60°C, and the pH value of the precipitation process was 7.0 (wherein, according to the pH value of the precipitation process, the amount of sodium carbonate aqueous solution was controlled to be 105% of the theoretically required amount ...

Embodiment 2

[0090] (1) Add 300g of water, 2g of dimethyltetradecyl[3-(trimethoxysilyl)propyl]ammonium chloride and 6g of hydroxyethyl methylcellulose into the reaction kettle and stir evenly to obtain a dispersion I.

[0091] (2) 303.7g copper nitrate (Cu(NO 3 ) 2 ·3H 2 O, 242), 87.4g zinc nitrate (Zn(NO 3 ) 2 ·6H 2 O, 298) and 348.8g aluminum nitrate (Al(NO 3 ) 3 9H 2 (2, 375) was dissolved in 1661.5g water to prepare a mixed salt solution, and the preparation concentration was an aqueous sodium carbonate solution of 15wt%, and the above two solutions were heated to 65° C. and then added dropwise to the aforementioned reaction kettle in parallel, and the dropping time was 50 minutes. , control the temperature of the precipitation process at 65°C, and the pH value of the precipitation process is 7.0 (wherein, according to the pH value of the precipitation process, the amount of sodium carbonate aqueous solution is controlled to be 105% of the theoretically required amount for the ...

Embodiment 3

[0098] (1) Add 300g of water, 1g of dimethylhexadecyl[3-(trimethoxysilyl)propyl]ammonium chloride and 3g of hydroxyethyl methylcellulose into the reaction kettle and stir evenly to obtain a dispersion I.

[0099] (2) 334.1g copper nitrate (Cu(NO 3 ) 2 ·3H 2 O, 242), 107.8g zinc nitrate (Zn(NO 3 ) 2 ·6H 2 O, 298) and 161.9g aluminum nitrate (Al(NO 3 ) 3 9H 2 (2, 375) was dissolved in 1661.5g water to prepare mixed salt solution, and the preparation concentration was 15wt% sodium carbonate aqueous solution, the above two solutions were heated to 65°C respectively and then added dropwise to the aforementioned reaction kettle in parallel, and the dropping time was 60min , control the temperature of the precipitation process to 65°C, and the pH value of the precipitation process to be 7.0 (wherein, according to the pH value of the precipitation process, the amount of sodium carbonate aqueous solution is controlled to be 105% of the theoretically required amount to completel...

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Abstract

The invention discloses a catalyst for preparing trimethylolpropane through hydrogenation of 2,2-dimethylolbutyraldehyde and a preparation method of the catalyst. The catalyst comprises 35 to 70 wt% of copper oxide, 5 to 25 wt% of zinc oxide, 5 to 35 wt% of aluminum oxide, 10 to 30 wt% of silicon dioxide, 0.5 to 5 wt% of alkaline earth metal oxide, 0.05 to 1.0 wt% of palladium oxide, 0.01 to 1.0 wt% of iridium oxide and 0.01 to 1.0 wt% of tin oxide. When the catalyst is used for preparing trimethylolpropane by a hydrogenation method, the catalyst not only has good activity and selectivity, butalso has strong formate conversion capability and high mechanical stability.

Description

technical field [0001] The invention belongs to the technical field of catalysis, and relates to a hydrogenation catalyst and its preparation method and application, in particular to a catalyst for preparing trimethylolpropane by hydrogenation of 2,2-dimethylolbutyraldehyde and the preparation method thereof. Background technique [0002] Trimethylolpropane (TMP for short), also known as trimethylolpropane and 2,2-dimethylolbutanol, is mainly used in the synthesis of high-grade alkyd resins and polyurethane coatings, and can also be used in the synthesis of plasticizers, aviation lubricants, Surfactants, wetting agents, textile auxiliaries, printing inks and a variety of fine chemicals, etc., have broad market prospects. [0003] At present, there are two main methods for preparing trimethylolpropane: disproportionation method and catalytic hydrogenation method. The disproportionation method is that 2,2-dimethylolbutyraldehyde (DMB) generated from formaldehyde and n-butyral...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/89C07C29/141C07C31/22
CPCB01J23/002B01J23/8966C07C29/141B01J2523/00B01J35/394B01J2523/17B01J2523/27B01J2523/31B01J2523/22B01J2523/41B01J2523/824B01J2523/827B01J2523/43C07C31/22
Inventor 李作金于海波詹吉山沙宇燕宸孙康初乃波黎源
Owner WANHUA CHEM GRP CO LTD
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