Method for preparing proton exchange film based on con-radiation technology

A technology of proton exchange membrane and base membrane, which is applied in fuel cell components, fuel cells, electrochemical generators, etc., can solve the problems of difficult particle size control, affecting performance, incompatibility, etc., and achieve good chemical stability Sex and thermal stability, improve high temperature water retention performance, and prevent the loss of water

Inactive Publication Date: 2009-08-19
BEIJING RADIATION APPL RES CENT
View PDF4 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The proton exchange membrane of the present invention has high moisturizing performance and dimensional stability, but the inorganic component palygorskite-sepiolite group mineral fiber is incompatible with the proton exchange resin solution, and it is difficult to achieve good dispersion
Another example is the invention patent of Xinyuan Power Co., Ltd. "a carbon nanotube-reinforced self-humidifying composite proton exchange membrane and its preparation" ([application number] 200610134078.8), which uses a solution casting method to obtain carbon nanotube-reinforced perfluorosulfur Acid resin membrane, and then introduce Pt into the membrane as a self-humidifying catalyst, wherein Pt is loaded on carbon nanotubes to obtain a composite proton exchange membrane with good strength and self-humidification, but carbon nanotubes loaded with inorganic components Pt are easy Agglomeration, affecting performance, at the same time, the price of perfluorosulfonic acid resin, Pt and carbon nanotubes used is still high
"A preparation method for core components of water-retaining proton exchange membrane fuel cells" invented by Wuhan University of Technology ([Application No.] 200710051758.8), first adjust the pH value of the proton-conducting polymer solution with NaOH, add anhydrous organic solvent, and then distill, The inorganic oxide precursor is added to the distilled solution and stirred to obtain a proton-conducting polymer modified with inorganic oxide nanoparticles, and a fuel cell core component with good water retention capacity is prepared, but there are still nanoparticles that are easy to agglomerate. Difficult to control particle size
The organic-inorganic phase of the proton exchange membrane obtained by the above method is mainly combined by weak interactions such as physical adsorption, hydrogen bond or van der Waals force. In the application of fuel cells, due to penetration or diffusion, the inorganic components are easily transported from The organic polymer phase is separated, and the weak interfacial interaction between the organic-inorganic phase will directly affect the structure and performance of the proton exchange membrane

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] (1) Polymer base film polytetrafluoroethylene was washed with acetone to remove impurities on the film surface, dried, and stored in a desiccator for later use.

[0030] (2) Mix the graft monomer p-styryltrimethoxysilane and divinylbenzene with a molar ratio of 1:0.5 and the solvent toluene to prepare a solution with a concentration of 0.5mol / L.

[0031] (3) Immerse the polymer base film obtained in the step (1) into the monomer solution in the step (2), fill it with nitrogen and seal it.

[0032] (4) Co-radiation grafting at room temperature, the radiation source is Co-60, and the radiation dose is 40kGy.

[0033] (5) The radiation-grafted film was extracted twice for 48 hours with the solvent methylene chloride through a Soxhlet extractor to wash away the copolymer, and then dried.

[0034] (6) The dried grafted membrane is placed in 0.2M chlorosulfonic acid 1,2-dichloroethane solution, stirred and reacted for 30h to carry out sulfonation treatment, the membrane afte...

Embodiment 2

[0054] (1) Select polymer base film polyvinylidene fluoride to wash off the dirt on the surface of the film with acetone, then dry it and store it in a desiccator for later use.

[0055] (2) Mix the graft monomer p-styryltrimethoxysilane and divinylbenzene with a molar ratio of 1:4 and the solvent dichloromethane to prepare a solution with a concentration of 3 mol / L.

[0056] (3) Immerse the polymer base film obtained in the step (1) into the monomer solution in the step (2), fill it with nitrogen and seal it.

[0057] (4) Co-radiation grafting at room temperature, the radiation source is Co-60, and the radiation dose is 5kGy.

[0058] (5) Radiation-grafted membrane was extracted twice for 48 hours with the solvent tetrahydrofuran through a Soxhlet extractor, the copolymer was washed away, and dried.

[0059] (6) The dried grafted membrane was placed in a 0.8M solution of chlorosulfonic acid in dichloromethane, stirred and reacted for 18 hours for sulfonation treatment, the s...

Embodiment 3

[0063] (1) Select the polymer base film polyethylene-tetrafluoroethylene copolymer, wash off the dirt on the surface of the film with dichloromethane, dry it, and store it in a desiccator for later use.

[0064] (2) Mix the graft monomer p-styryltrimethoxysilane and divinylbenzene with a molar ratio of 1:2 and solvent ethanol to prepare a solution with a concentration of 1mol / L.

[0065] (3) Immerse the polymer base film obtained in the step (1) into the monomer solution in the step (2), fill it with nitrogen and seal it.

[0066] (4) Co-radiation grafting at room temperature, the radiation source is an electron accelerator, and the radiation dose is 10kGy.

[0067] (5) The radiation grafted film was extracted twice for 48 hours with solvent acetone through a Soxhlet extractor, the copolymer was washed away, and dried.

[0068] (6) The dried grafted membrane was sulfonated with 50% oleum, and the sulfonated condition was 75 hours at room temperature. The sulfonated membrane w...

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 relates to a preparation method of a proton exchange membrane, in particular to a preparation method of the proton exchange membrane based on co-radiation technology. The preparation method pertains to the technical field of high polymer materials. The preparation method comprises the following steps: co-radiation grafting is achieved among a polymer basement membrane, a monomer p-styryl trimethoxysilane and divinylbenzene by adopting the co-radiation grafting method; the sulfonation is carried out to the radiation grafting membrane; and the target product, namely the proton exchange membrane, is formed by the hydrolysis-polycondensation reaction between the sulfonated membrane and the hydrochloric solution. The proton exchange membrane obtained by the method is introduced with base group which forms strong chemical bonds with the polymer basement membrane and has water holding function, thus improving the water holding performance and the mechanical strength of the membrane and having better size stability and proton conductivity. For the co-radiation grafting method provided by the invention, a chemical initiating agent is not required and the co-radiation grafting method can be finished under room temperature, the performance of the membrane can be improved and the grafting rate of the reaction can be controlled by adjusting such parameters as the irradiation dose, dose rate, the monomer concentration and so on. Therefore, the co-radiation grafting method is an effective method for preparing the proton exchange membrane with high quality, homogeneous phase and low cost.

Description

technical field [0001] The invention relates to a method for preparing a proton exchange membrane, in particular to a method for preparing a proton exchange membrane based on co-radiation technology, and belongs to the field of polymer materials. Background technique [0002] A fuel cell is a device that converts chemical energy into electrical energy. It uses hydrogen, natural gas, coal gas or methanol and other non-petroleum fuels to undergo oxidation-reduction reactions at the two poles of the battery with pure oxygen or air to provide direct current for the environment. According to the electrolyte in fuel cells, fuel cells can be roughly divided into alkaline fuel cells (AFC), phosphoric acid fuel cells (PAFC), solid oxide fuel cells (SOFC), molten carbonate fuel cells (MCFC) and Proton Exchange Membrane Fuel Cell (PEMFC). Among them, the proton exchange membrane fuel cell has the advantages of low operating temperature, fast start-up, high output specific power, and ...

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): H01M8/02C08J7/18H01M8/1072H01M8/1088
CPCY02E60/50
Inventor 于宏燕石建恒曾心苗许自炎鲍矛
Owner BEIJING RADIATION APPL RES CENT
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products