Method for preparing graphene porous membrane

A graphene and porous membrane technology, applied in the field of materials, can solve the problems of porous membrane volume expansion, non-uniform pore size, high energy consumption, etc., and achieve the effects of preventing fine deformation, simple instrument operation, and increasing the amount of material fed.

Inactive Publication Date: 2017-02-15
SHANDONG UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method has obvious disadvantages: first, it consumes a lot of energy and the treatment conditions are harsh; second, the heat treatment process will cause the volume expansion of the porous membrane; Inhomogeneity, this uncontrollable and disordered structure is not conducive to researchers' research and understanding of the storage and transport principles of substances in porous structures
However, the method of preparing graphene porous membrane by organic solvent dissolution combined with critical point drying has not been reported yet.

Method used

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  • Method for preparing graphene porous membrane
  • Method for preparing graphene porous membrane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] (1) Add 50 mg of graphite oxide to 50 mL of water to obtain a graphite oxide dispersion, and ultrasonically disperse for 1 h to obtain a graphene oxide solution;

[0027] (2) adding 1 g of polystyrene microspheres to the above graphene oxide solution, so that the polystyrene microspheres are uniformly dispersed in the graphene oxide, and dried to obtain a composite film of graphene oxide and polystyrene microspheres;

[0028] (3) The composite film of graphene oxide and polystyrene microspheres was reduced by using 0.2L of hydroiodic acid solution with a concentration of 57% by volume, the reaction temperature was 80°C, the reduction time was 2h, and washed to obtain graphite. Composite film of alkene and polystyrene microspheres;

[0029] (4) The polystyrene microspheres were removed with tetrahydrofuran, and the tetrahydrofuran was replaced with anhydrous ethanol several times. The treated samples were stored in anhydrous ethanol and further treated by critical point ...

Embodiment 2

[0031] (1) Add 500 mg of graphite oxide to 50 mL of water to obtain a graphite oxide dispersion, and ultrasonically disperse for 5 hours to obtain a graphene oxide solution;

[0032] (2) Add 0.05g polymethyl methacrylate microspheres to the above graphene oxide solution, so that the polymethyl methacrylate microspheres are uniformly dispersed in the graphene oxide, and suction filtration to obtain graphene oxide and polymethyl methacrylate. Composite film of methyl acrylate microspheres;

[0033] (3) The composite film of graphene oxide and polymethyl methacrylate microspheres was reduced by using 5L of hydroiodic acid solution with a concentration of 40% by volume, the reaction temperature was 100°C, the reduction time was 8h, washed, A composite film of graphene and polymethyl methacrylate microspheres is obtained;

[0034] (4) The polymethyl methacrylate microspheres were removed with toluene, and the toluene was replaced with anhydrous ethanol several times. The treated s...

Embodiment 3

[0036] (1) Add 200 mg of graphite oxide to 50 mL of water to obtain a graphite oxide dispersion, and ultrasonically disperse for 1.5 h to obtain a graphene oxide solution;

[0037] (2) Add 0.1 g of poly[styrene-methyl methacrylate-acrylic acid] microspheres to the above graphene oxide solution, so that the poly[styrene-methyl methacrylate-acrylic acid] microspheres are uniformly dispersed in the graphite oxide. and drying to obtain a composite film of graphene oxide and poly[styrene-methyl methacrylate-acrylic acid] microspheres;

[0038] (3) The composite film of graphene oxide and poly[styrene-methyl methacrylate-acrylic acid] microspheres was reduced by using 0.5L of a hydroiodic acid solution with a concentration of 47% by volume, and the reaction temperature was 90 °C , the reduction time is 4h, and washing is performed to obtain a composite film of graphene and poly[styrene-methyl methacrylate-acrylic acid] microspheres;

[0039] (4) Remove the poly[styrene-methyl metha...

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Abstract

The invention provides a method for preparing a graphene porous membrane. The method includes the steps that oxidized graphite is added into water, oxidized graphite dispersion liquid is obtained and subjected to ultrasonic dispersion, and an oxidized graphene solution is obtained; a pore forming agent is added into the oxidized graphene solution and evenly dispersed into oxidized graphene, the mixture is subjected to suction filtration and/or dried, and a composite membrane of the oxidized graphene and the pore forming agent is obtained; the composite membrane of the oxidized graphene and the pore forming agent is reduced and washed, and a composite membrane of graphene and the pore forming agent is obtained; the pore forming agent is removed with an organic solvent, and under the moist condition, the product is further treated with the critical point drying method, and the graphene porous membrane is obtained; the pore forming agent is one or more of homopolymer microspheres and copolymer microspheres. The size of pores inside the graphene porous membrane prepared with the method ranges from 100 nm to 1,000 nm, the porosity can be regulated and controlled by regulating the concentration or the size of the pore forming agent, the yield of the graphene porous membrane is high, and an operating device is simple.

Description

technical field [0001] The invention belongs to the technical field of materials, and in particular relates to a preparation method of a graphene porous membrane. Background technique [0002] Graphene is a two-dimensional honeycomb grid structure composed of a single atomic layer of carbon. Its unique atomic structure and electronic structure enable the material to have excellent electrical, thermal and mechanical properties, as well as a large theoretical specific surface area (theoretical calculation). The value is 2600m 2 / g), which is the best choice for a new generation of supercapacitor electrode materials. However, the incomplete reduction degree of graphene and the stacking due to van der Waals forces during the reduction process lead to poor conductivity of the material, and the specific surface area is much lower than the theoretical value, thus affecting the final performance. [0003] In order to further reduce the stacking of graphene and increase the specifi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B32/184
CPCC01P2004/03
Inventor 辛伍红赵增典冯柳
Owner SHANDONG UNIV OF TECH
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