Preparation method and application of boron nitride loaded Ni-MoOx nano catalyst

A nano-catalyst, boron nitride technology, applied in the field of catalyst preparation and sustainable development of the environment and energy, can solve the problems that limit the large-scale practical application of noble metal-based catalysts, low catalyst utilization, high cost, etc., achieve short synthesis time, Reduced crystallinity and easy operation

Active Publication Date: 2018-11-06
JILIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] At present, almost all catalysts used for the complete decomposition of hydrazine borane contain noble metal components, but problems such as high cost and limited reserves limit the large-scale practical application of noble metal-based catalysts.
However, in the reported non-precious metal catalysts, most of the conversions are only 50%, making the utilization of catalysts low.

Method used

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  • Preparation method and application of boron nitride loaded Ni-MoOx nano catalyst
  • Preparation method and application of boron nitride loaded Ni-MoOx nano catalyst
  • Preparation method and application of boron nitride loaded Ni-MoOx nano catalyst

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Experimental program
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Effect test

Embodiment 1

[0029] Such as figure 1 As shown, a boron nitride supported Ni-MoO x The preparation method of nanometer catalyst comprises the following steps:

[0030] Step 1. Prepare 15 mg of an aqueous solution of hexagonal boron nitride BN with a concentration of 0.5 to 6 mg / mL, and obtain a uniformly dispersed hexagonal boron nitride BN aqueous solution after ultrasonic treatment for 15 to 120 minutes;

[0031] Step two, the NiCl of 0.1mmol 2 , added to the BN aqueous solution in step 1, and continued to stir for 1 to 10 minutes to obtain a mixed solution A;

[0032] Step 3, then 0.1mmol of Na 2 MoO 4 Add to the mixed solution A in step 2, and continue to stir to obtain the mixed solution B; and the molar ratio of Ni:Mo is 1:1;

[0033] Step four, 30mg sodium borohydride NaBH 4Dissolve in 1mL of distilled water, add as a reducing agent to the mixed solution B in step 3, stir at 25°C for 5-15min for reduction reaction, and obtain boron nitride-supported Ni-MoO x nanocatalyst.

[...

Embodiment 2

[0036] A Boron Nitride Supported Ni-MoO x The preparation method of nanometer catalyst comprises the following steps:

[0037] Step 1. Prepare 15 mg of an aqueous solution of hexagonal boron nitride BN with a concentration of 0.5 to 6 mg / mL, and obtain a uniformly dispersed hexagonal boron nitride BN aqueous solution after ultrasonic treatment for 15 to 120 minutes;

[0038] Step two, the NiCl of 0.05mmol 2 Add the aqueous solution to the BN aqueous solution in step 1, and continue to stir for 1 to 10 minutes to obtain the mixed solution A;

[0039] Step 3, then 0.05mmolNa 2 MoO 4 Add the aqueous solution to the mixed solution A in step 2, and continue to stir to obtain the mixed solution B; and the molar ratio of Ni:Mo is 1:1;

[0040] Step four, 20mg sodium borohydride NaBH 4 Dissolve in 1mL of distilled water, add to the mixed solution B in step 3 as a reducing agent, stir at room temperature for 5-15min for reduction reaction, and obtain boron nitride supported Ni-MoO...

Embodiment 3

[0042] A Boron Nitride Supported Ni-MoO x The preparation method of nanometer catalyst comprises the following steps:

[0043] Step 1. Prepare 15 mg of an aqueous solution of hexagonal boron nitride BN with a concentration of 6 mg / mL, and obtain a uniformly dispersed hexagonal boron nitride BN aqueous solution after ultrasonic treatment for 15 to 120 minutes;

[0044] Step two, the NiCl of 0.5mmol 2 Add the aqueous solution to the BN aqueous solution in step 1, and continue to stir for 1 to 10 minutes to obtain the mixed solution A;

[0045] Step 3, then 0.5mmol of Na 2 MoO 4 Add the aqueous solution to the mixed solution A in step 2, and continue to stir to obtain the mixed solution B; and the molar ratio of Ni:Mo is 1:1;

[0046] Step four, 60mg sodium borohydride NaBH 4 Dissolve in 1mL of distilled water, add to the mixed solution B in step 3 as a reducing agent, stir at room temperature for 5-15min for reduction reaction, and obtain boron nitride supported Ni-MoO x n...

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Abstract

The invention discloses a preparation method and application of a boron nitride loaded Ni-MoOx nano catalyst. The preparation method comprises the following steps: preparing an aqueous solution of hexagonal boron nitride BN, and ultrasonically treating to obtain a uniformly dispersed hexagonal boron nitride BN aqueous solution; adding a NiCl2 aqueous solution into the BN aqueous solution in step I, and continuously stirring to obtain a mixed solution A; adding a Na2MoO4 aqueous solution into the mixed solution A, and continuously stirring to obtain a mixed solution B; adding 20-60 mg of sodiumborohydride NaBH4 into the mixed solution B, stirring for 5-15 minutes to perform reduction reaction, thereby obtaining the boron nitride loaded Ni-MoOx nano catalyst. The preparation method adopts aone-step quick reduction method to synthesize the boron nitride loaded Ni-MoOx nano catalyst, can be completed at room temperature and has the advantages of being short in synthetic time, simple andconvenience in operation and the like; the synthesized Ni-MoOx/BN catalyst can be used for catalyzing decomposition of hydrazine borane water solution 323K to produce hydrogen and the catalyst still has a 100% conversion rate in case of not adding any additive, 100% hydrogen gas selectivity, relatively good circulating stability and extremely high catalytic activity.

Description

technical field [0001] The invention relates to the field of catalyst preparation and the sustainable development of the environment and energy, in particular to a boron nitride supported Ni-MoO x Preparation methods and applications of nanocatalysts. Background technique [0002] As a clean and efficient green energy, hydrogen energy has attracted extensive research interest, and it can be widely used in power generation and fuel cells and other fields. However, traditional high-pressure tanks and low-temperature liquid hydrogen storage methods have disadvantages such as low efficiency, poor safety, and high cost. Therefore, the development of safe and efficient hydrogen storage methods is a current research hotspot. [0003] Hydrazine borane (N 2 h 4 BH 3 , HB), which is a safe and stable solid at room temperature with a hydrogen content as high as 15.4 wt%, and thus is considered as a promising chemical hydrogen storage material. Complete decomposition of hydrazine b...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J27/24C01B3/06H01M8/0656
CPCB01J23/002B01J27/24B01J35/0013C01B3/065H01M8/0656Y02E60/36Y02E60/50
Inventor 鄢俊敏李思佳康霞易莎莎乌兰巴日段焱鑫姚佳欣蒋青
Owner JILIN UNIV
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