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A kind of hydrophobic lipophilic hydrodeoxygenation catalyst and its preparation method and application

A deoxygenation catalyst, hydrophobic and lipophilic technology, applied in chemical instruments and methods, physical/chemical process catalysts, preparation of liquid hydrocarbon mixtures, etc., can solve the problems of low catalytic activity and high crystallinity of catalysts, and achieve simple operation and low price. , to avoid damaging effects

Inactive Publication Date: 2019-07-26
XIANGTAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The preparation of bimetallic sulfide catalysts currently used in industry mainly adopts high-temperature reduction sulfurization method, and the prepared catalysts have high crystallinity and low catalytic activity

Method used

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  • A kind of hydrophobic lipophilic hydrodeoxygenation catalyst and its preparation method and application

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Dissolve 0.725 g of sodium molybdate in 80 mL of deionized water, add 0.6851 g of thiourea, and then add 8.02 g of silicotungstic acid. After fully dissolving, move it to a 200 mL airtight hydrothermal reaction kettle, seal it, and react at 240°C for 12 hours Afterwards, the temperature was lowered to 50° C., and the lid of the reaction kettle was opened. Dissolve 0.0873 g of cobalt nitrate in 5 ml of deionized water, add 0.0457 g of thiourea to dissolve, add this solution into the previously opened reactor, seal it, and react at 240 °C for 12 hours. After the reaction, a black precipitate is obtained. After washing with water and alcohol, dry in a vacuum oven at 60°C for 5 hours.

[0029] Add 12.5 g of n-dodecane, 5.4 g of p-ethylphenol and 0.03 g of the above-prepared catalyst in the autoclave, install the device, remove the air in the autoclave by displacement method, and then change from room temperature at a rate of 10 °C / min to The temperature was increased to 22...

Embodiment 2

[0031] Dissolve 0.725 g of sodium molybdate in 80 mL of deionized water, add 0.6851 g of thiourea, and then add 8.02 g of silicotungstic acid. After fully dissolving, move it to a 200 mL airtight hydrothermal reaction kettle, seal it, and react at 240°C for 12 hours Afterwards, the temperature was lowered to 50° C., and the lid of the reaction kettle was opened. Dissolve 0.1746 g of cobalt nitrate in 5 ml of deionized water, add 0.0914 g of thiourea to dissolve, then add this solution into the previously uncapped reaction kettle, seal it, and react at 240 °C for 12 hours. After the reaction, a black precipitate is obtained. After washing with water and alcohol, dry in a vacuum oven at 60°C for 5 hours.

[0032] Add 12.5 g of n-dodecane, 5.4 g of p-ethylphenol and 0.03 g of the above-prepared catalyst in the autoclave, install the device, remove the air in the autoclave by displacement method, and then change from room temperature at a rate of 10 °C / min to Raise it to 225 °C, ...

Embodiment 3

[0034] Dissolve 0.725 g of sodium molybdate in 80 mL of deionized water, add 0.6851 g of thiourea, and then add 8.02 g of silicotungstic acid. After fully dissolving, move it to a 200 mL airtight hydrothermal reaction kettle, seal it, and react at 240°C for 12 hours Afterwards, the temperature was lowered to 50° C., and the lid of the reaction kettle was opened. Dissolve 0.2619 g of cobalt nitrate in 5 ml of deionized water, add 0.137 g of thiourea to dissolve, then add this solution into the previously opened reaction kettle, seal it, and react at 240 °C for 12 hours. After the reaction, a black precipitate is obtained. After washing with water and alcohol, dry in a vacuum oven at 60°C for 5 hours.

[0035]Add 12.5 g of n-dodecane, 5.4 g of p-ethylphenol and 0.03 g of the above-prepared catalyst in the autoclave, install the device, remove the air in the autoclave by displacement method, and then change from room temperature at a rate of 10 °C / min to The temperature was incr...

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Abstract

The invention discloses a hydrophobic and lipophilic hydrodeoxygenation catalyst, as well as a preparation method and an application of the catalyst. The catalyst is prepared by two steps by a liquid phase method. The preparation method comprises the steps of dissolving molybdenum salt and a sulfur source in a solvent, adding heteropoly acid, performing a sealed heating reaction, adding a solution containing cobalt salt and the sulfur source, and then continuing to perform a sealed heating reaction. The preparation method of the catalyst is simple and environmentally friendly; the prepared catalyst has better hydrophobicity and lipophilicity; in hydrodeoxygenation reaction processes of catalytic biomass oil and an oxygen-containing compound of the catalytic biomass oil, dispersion of the catalyst in an organic solvent can be facilitated; contact of water and the catalyst is prevented; damage of the water on a catalyst structure is avoided; a deoxygenation rate and the stability of the catalyst are increased and improved.

Description

technical field [0001] The invention belongs to the field of oil refining, and in particular relates to a hydrophobic and lipophilic hydrodeoxygenation catalyst and its preparation method and application, which are specifically used in the catalytic hydrodeoxygenation reaction of oxygen-containing compounds in biomass oil. Background technique [0002] Bio-oil has become one of the most potential energy alternatives to petroleum because of its renewable and extensive raw materials. However, bio-oil contains a large amount of oxygen-containing compounds such as phenols, furans, aldehydes, and ketones, and the oxygen content is as high as 50%, resulting in low combustion calorific value, poor mutual solubility, and high viscosity. Catalytic hydrodeoxygenation (HDO) is required to Improve oil quality. During the hydrodeoxygenation process, the oxygen atom ends up as H 2 The form of O is removed, and the generated water will compete for adsorption on the surface of the catalys...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/051C10G3/00
CPCY02P30/20
Inventor 王威燕仵奎杨运泉郭宣霖
Owner XIANGTAN UNIV