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Preparation method of high-activity CoB catalyst

A catalyst and high-activity technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of slow hydrogen production rate in hydrolysis reaction, easy agglomeration of catalyst particles, Unsatisfactory catalyst performance and other problems, to achieve the effect of fast reaction speed, excellent catalytic hydrogen production performance, and complete recovery

Pending Publication Date: 2022-01-28
XIAN TECHNOLOGICAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] For NaBH 4 CoB-based catalysts for hydrogen production by hydrolysis are usually prepared by chemical reduction, but the catalyst particles are easy to agglomerate during the preparation process, which reduces the effective surface area and the number of active sites, resulting in unsatisfactory catalyst performance. 4 The hydrogen production rate of the hydrolysis reaction is slow

Method used

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  • Preparation method of high-activity CoB catalyst
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  • Preparation method of high-activity CoB catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Embodiment 1 A kind of preparation method of highly active CoB catalyst

[0038] This embodiment is a highly active CoB catalyst, which is carried out in sequence according to the following steps:

[0039] A kind of preparation method of highly active CoB catalyst is characterized in that, carries out successively according to following step order:

[0040] (1) Weigh cobalt chloride hexahydrate, place it in a mortar, and mechanically grind it at a speed of 4rad / s for 20min to obtain A1;

[0041] (2) Slowly add urea to A1, the molar ratio of urea to cobalt chloride hexahydrate is 56:1, and fully grind together in a mortar to a particle size of 80-100 mesh, the grinding speed is 4rad / s, to two After they are mixed evenly, B1 is obtained;

[0042] (3) Sodium borohydride is evenly dispersed on the surface of B1 at 1.2g / min, the molar ratio of sodium borohydride to cobalt chloride hexahydrate is 5:1, and it is fully ground while adding, and the grinding speed is 6rad / s, un...

Embodiment 2-4

[0049] The preparation method of the highly active CoB catalyst of embodiment 2-4

[0050] This example is a preparation method of a highly active CoB catalyst. The preparation process and detection process are similar to those of Example 1. The only difference is that the corresponding technical parameters in the preparation process are different, as follows:

[0051]

[0052]

Embodiment 5

[0053] Embodiment 5 comparative example

[0054] In order to explore the influence of different conditions on the preparation of CoB catalysts, the following comparative experiments were carried out in this example, specifically as follows:

[0055] Group A: The preparation process of the CoB catalyst is similar to that of Example 1, except that no urea is added in the process. The XPS analysis of this sample (such as Figure 7 ) shows that the content of metal Co on the surface of the catalyst is only 45.8%, compared with the CoB catalyst prepared in Example 1, the active Co sites that exist are significantly reduced, and correspondingly, the performance of catalytic hydrolysis for hydrogen production is significantly reduced.

[0056] Group B: The preparation process of the CoB catalyst is similar to that of Example 1, except that the molar ratio of urea to cobalt chloride hexahydrate is 39:1.

[0057] Group C: The preparation process of the CoB catalyst is similar to that...

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Abstract

The invention discloses a preparation method of a high-activity CoB catalyst, which comprises the following steps of: weighing cobalt chloride hexahydrate, putting the cobalt chloride hexahydrate into a mortar, conducting mechanical grinding, slowly adding urea into the cobalt chloride hexahydrate, and fully grinding the cobalt chloride hexahydrate and the urea in the mortar until the cobalt chloride hexahydrate and the urea are uniformly mixed; uniformly dispersing sodium borohydride into the mixture, and fully conducting grinding while adding until the mixture is completely blackened to obtain a reaction product; and transferring the reaction product into another container, adding distilled water, conducting centrifuging, separately conducting washing with ethanol and distilled water for three times, and carrying out vacuum drying on the obtained solid at 60 DEG C for 12 hours to obtain the high-activity CoB catalyst. The CoB catalyst with strong ferromagnetism and excellent catalytic hydrogen production performance is synthesized through solid reaction at room temperature, the prepared catalyst is spherical particles with uniform morphology, the particle size is 30-50 nm, the preparation method is simple, the process is easy to control, the solid reaction process is short, and the reaction speed is high.

Description

technical field [0001] The invention belongs to the field of catalytic hydrogen production materials, and in particular relates to a preparation method of a highly active CoB catalyst. Background technique [0002] With the intensification of global energy crisis and environmental pollution, hydrogen energy has attracted widespread attention due to its clean, efficient and renewable advantages. Considering the storage and transportation of hydrogen energy, chemical hydrides are considered as ideal hydrogen storage materials. Sodium borohydride (NaBH 4 ) has attracted special attention due to its high hydrogen storage capacity (10.8 wt.%), controllable hydrogen production rate, and non-toxic by-products. while NaBH 4 It is necessary to promote its hydrolysis reaction under the action of a suitable catalyst to efficiently release pure hydrogen at room temperature. Therefore, the development of high-efficiency catalysts is very important for NaBH 4 Hydrogen production from ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/75B01J35/08B01J35/10C01B3/06
CPCB01J23/75C01B3/065B01J35/23B01J35/33B01J35/51B01J35/613Y02E60/36
Inventor 士丽敏陆晨滢王宇晶魏攀
Owner XIAN TECHNOLOGICAL UNIV
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