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Micro-oxidized conductive carbon black supported nano metal bismuth catalyst and application thereof

A technology of conductive carbon black and nano metal, applied in the field of catalytic chemistry, can solve the problems of low activation ability of nitrogen molecules, lack of practical value, strong competition for hydrogen evolution reaction, etc., and achieve the effect of promoting reaction activity, improving selectivity and wide application prospect.

Inactive Publication Date: 2019-06-21
BEIJING INSTITUTE OF TECHNOLOGYGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, the existing electrocatalytic ammonia synthesis catalysts all show very low ammonia synthesis selectivity (10%) and reaction rate, making these electrocatalytic systems lack real practical value
There are two main reasons for the low selectivity, energy efficiency and reaction rate of the existing electrochemical ammonia synthesis system: one is the low activation ability of nitrogen molecules in the existing catalysts, and the other is the strong competition of the hydrogen evolution reaction in the aqueous solution.
The methods reported so far cannot solve the above problems well, so it is impossible to achieve highly selective and efficient electrocatalytic synthesis of ammonia.

Method used

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  • Micro-oxidized conductive carbon black supported nano metal bismuth catalyst and application thereof
  • Micro-oxidized conductive carbon black supported nano metal bismuth catalyst and application thereof
  • Micro-oxidized conductive carbon black supported nano metal bismuth catalyst and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] (1) get 10g conductive carbon black (conductive carbon black uses the acetylene black type conductive carbon black that Alfa company produces), soak and wash three times with hot nitric acid (mass fraction is 20%) of 50-70 degree Celsius, then use deionized water Wash it to neutral and dry it in the shade at room temperature. Take 2 g of the above-mentioned treated conductive carbon black in a three-necked flask, add 80 mL of concentrated sulfuric acid (98% by mass) and stir at room temperature for 12 hours. Subsequently, the three-necked flask was placed in an ice-water bath, and 2 g of ground potassium permanganate powder was slowly added into the three-necked flask, and the whole process lasted for about 1 hour. After the addition was complete, the temperature of the reaction system was raised to 35° C., and the reaction was continued at this temperature for 90 minutes. Subsequently, 160 mL of deionized water was slowly added into the three-necked flask four times, ...

Embodiment 2

[0046] (1) get 10g conductive carbon black (conductive carbon black uses the acetylene black type conductive carbon black that Alfa company produces), soak and wash three times with hot nitric acid (mass fraction is 20%) of 50-70 degree Celsius, then use deionized water Wash it to neutral and dry it in the shade at room temperature. Take 2 g of the above-mentioned treated conductive carbon black in a three-necked flask, add 80 mL of concentrated sulfuric acid (98% by mass) and stir at room temperature for 12 hours. Subsequently, the three-necked flask was placed in an ice-water bath, and 2 g of ground potassium permanganate powder was slowly added into the three-necked flask, and the whole process lasted for about 1 hour. After the addition was complete, the temperature of the reaction system was raised to 35° C., and the reaction was continued at this temperature for 90 minutes. Subsequently, 160 mL of deionized water was slowly added into the three-necked flask four times, ...

Embodiment 3

[0052] (1) get 10g conductive carbon black (conductive carbon black uses the acetylene black type conductive carbon black that Alfa company produces), soak and wash three times with hot nitric acid (mass fraction is 20%) of 50-70 degree Celsius, then use deionized water Wash it to neutral and dry it in the shade at room temperature. Take 2 g of the above-mentioned treated conductive carbon black in a three-necked flask, add 80 mL of concentrated sulfuric acid (98% by mass) and stir at room temperature for 12 hours. Subsequently, the three-necked flask was placed in an ice-water bath, and 2 g of ground potassium permanganate powder was slowly added into the three-necked flask, and the whole process lasted for about 1 hour. After the addition was complete, the temperature of the reaction system was raised to 35° C., and the reaction was continued at this temperature for 90 minutes. Subsequently, 160 mL of deionized water was slowly added into the three-necked flask four times, ...

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Abstract

The invention belongs to the field of catalysis chemistry and relates to a micro-oxidized conductive carbon black supported nano metal bismuth catalyst and an application thereof. In the catalyst, firstly, micro-oxidized conductive carbon black is prepared with an improved Hammer's method and then added to ethylene glycol or glycerol and sufficiently dispersed, then, bismuth nitrate pentahydrate is added, the mixture is stirred, a mixed dispersion liquid is obtained, and finally, the catalyst is obtained after the reaction in an airtight autoclave. Through ingenious micro oxidation treatment of the conductive carbon black, rich oxygen-containing functional groups are introduced on the surface while the conductivity is guaranteed, micro-oxidized conductive carbon black supported metal bismuth nanoparticles with uniform sizes are synthesized with a one-step solvothermal method and have excellent activity of electro-catalytic synthesis ammonia.

Description

technical field [0001] The invention belongs to the field of catalytic chemistry, and relates to a micro-oxidized conductive carbon black-loaded nano-metal bismuth catalyst and its application. Background technique [0002] The electrocatalytic ammonia synthesis reaction can reduce nitrogen in the atmosphere to ammonia substances that can be absorbed by plants at normal temperature and pressure. This kind of reaction can use water as a proton source and be driven by electricity generated by clean energy, so it is more energy-saving and environmentally friendly than the traditional Haber method (high temperature and high pressure reaction), showing great academic research value and application prospects. [0003] However, the existing electrocatalytic ammonia synthesis catalysts all show very low ammonia synthesis selectivity (10%) and reaction rate, which makes these electrocatalytic systems lack real practical value. There are two main reasons for the low selectivity, ener...

Claims

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Application Information

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IPC IPC(8): B01J23/18C25B11/06C25B1/00
Inventor 殷安翔郝宇晨步同安
Owner BEIJING INSTITUTE OF TECHNOLOGYGY
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