Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method for proton exchange membrane fuel cell catalyst

A proton exchange membrane and fuel cell technology, applied in chemical instruments and methods, physical/chemical process catalysts, battery electrodes, etc., can solve the problems of unfavorable catalyst industrial production, complex preparation process, difficult stabilizer removal, etc., to achieve safety and convenience Preparation efficiency, simple operation, and the effect of reducing catalyst agglomeration

Inactive Publication Date: 2015-05-06
KUNSHAN SUNLAITE NEW ENERGY +1
View PDF5 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

A kind of preparation method of Pt / C catalyst disclosed as Chinese patent CN103372429A, the catalytic active area of ​​the platinum-carbon catalyst prepared by the method is equivalent to that of the current commercial catalyst, yet, when the method prepares the catalyst, carbon black needs to be carried out For 2-6 hours of high-temperature calcination, after the reaction, the material needs to be placed for 2 days to allow the catalyst to settle, and then vacuum-dried for 4 hours. The time required to prepare a catalyst is too long and the efficiency is low, which is not conducive to the industrial production of the catalyst.
[0005] Chinese patent CN 1775362A discloses a preparation method for microwave synthesis of platinum / carbon nano-dot catalysts. The platinum nanoparticles in the synthesized Pt / C electrocatalyst have uniform particle size and good electrocatalytic performance. However, the preparation process The stabilizer is used in the process, which often makes it difficult to completely remove the stabilizer in the subsequent processing steps of the preparation process, and also makes the preparation process more complicated

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method for proton exchange membrane fuel cell catalyst
  • Preparation method for proton exchange membrane fuel cell catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] S1. Soak 1g of Vulcan XC-72R carbon black in a mixed solution of 3g of hydrogen peroxide and 3g of isopropanol, ultrasonically pretreat for 40min, with a power of 280W, filter under positive pressure, wash and dry in vacuum before use;

[0032] S2. Weigh 0.12 g of pretreated carbon black, add it to the sodium hydroxide solution, and ultrasonicate for 5 minutes;

[0033] S3, add 13g of deionized water, 28g of ethylene glycol, and 10.82g of chloroplatinic acid hexahydrate ethylene glycol solution with a mass fraction of 2% in turn in the beaker, and adjust the pH of the mixed slurry in the beaker to be 10;

[0034] S4, shear the slurry for 10 minutes, and ultrasonicate in an ice-water bath for 10 minutes to make the mixture uniform;

[0035] S5. Set the reaction temperature to 100°C, then heat with 700w microwave for 2.5min, cool the reaction solution to room temperature, add concentrated hydrochloric acid to adjust the pH value to 1, let it stand for 20min, filter, and w...

Embodiment 2

[0039] S1. Soak 1g of activated carbon in 3g of hydrogen peroxide and 9g of isopropanol, ultrasonically pretreat for 60min, filter under positive pressure, wash and dry in vacuum before use;

[0040] S2. Weigh 0.14 g of pretreated carbon black, add it to the sodium carbonate solution, and sonicate for 5 minutes;

[0041] S3. Add 12g deionized water, 21g ethylene glycol, and 8.12g mass fraction of 2% chloroplatinic acid hexahydrate ethylene glycol solution in the beaker, and adjust the pH of the mixed slurry in the beaker to 11;

[0042] S4, shear the slurry for 10 minutes, and ultrasonicate in an ice-water bath for 10 minutes to make the mixture uniform;

[0043] S5. Set the reaction temperature to 120°C, then heat with 800w microwave for 2 minutes, cool the reaction solution to room temperature, add concentrated hydrochloric acid to adjust the pH value to 2, let it stand for 20 minutes, filter, and wash repeatedly with deionized water until there is no chloride ion in the fil...

Embodiment 3

[0047] S1. Soak 1g of Vulcan XC-72R carbon black in a mixed solution of 3g of hydrogen peroxide and 4g of isopropanol, ultrasonically pretreat for 70min, filter under positive pressure, wash and dry in vacuum before use;

[0048] S2. Weigh 0.32 g of pretreated carbon black, add it to sodium hydroxide solution, and sonicate it in a 100 mL beaker for 8 min;

[0049]S3. Add 14g deionized water, 26g glycerol and 10.82g mass fraction of 2% chloroplatinic acid hexahydrate glycerin solution in the beaker in turn, and adjust the pH of the mixed slurry in the beaker to be 13;

[0050] S4, shear the slurry for 10 minutes, and ultrasonicate in an ice-water bath for 10 minutes to make the mixture uniform;

[0051] S5. Set the reaction temperature to 120°C, then heat with 700w microwave for 2.5min, cool the reaction solution to room temperature, add concentrated sulfuric acid to adjust the pH value to 2, let it stand for 20min, filter, and wash repeatedly with deionized water until there i...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a preparation method for a proton exchange membrane fuel cell catalyst. The adoption of a surfactant and a stabilizer is avoided, the preparation method is easy to operate, safe and convenient, and the preparation efficiency is greatly improved; acid is added as a precipitant, so that the precipitation time of the catalyst is greatly shortened, and the process efficiency is improved; a drying process of the catalyst is rapidly finished by a spray drying technology, and materials sprayed in the drying process are instantaneously heated by high temperature only when being sprayed into spray particles, so that the phenomenon of agglomeration of the catalyst is reduced, and the electrochemical activity of the platinum-carbon catalyst is kept high after the catalyst is dried; moreover, by the spray drying technology, the preparation time of the catalyst is further reduced, and the preparation method is easy to realize industrial production, and has broad market prospect.

Description

technical field [0001] The invention relates to a preparation method of a catalyst, in particular to a preparation method of a proton exchange membrane fuel cell catalyst, and belongs to the technical field of new materials. Background technique [0002] With the depletion of petrochemical energy and the increasing environmental pollution, people are paying more and more attention to the development and utilization of new energy. For many years, people have been trying to find energy utilization methods that have high energy utilization efficiency and do not pollute the environment. Among them, fuel cells are a new type of energy utilization methods that can directly convert chemical energy into electrical energy and have power generation efficiency. It is a new form of energy source with great development prospects. [0003] Proton exchange membrane fuel cell is a main force of fuel cell, and platinum carbon catalyst is one of its important components, accounting for about...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/42H01M4/92
CPCY02E60/50
Inventor 张洁姚颖方黄林陈佳范书琼刘建国
Owner KUNSHAN SUNLAITE NEW ENERGY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products