Method for preparing graphene through large-scale aqueous phase

A water-phase preparation, graphene technology, applied in the direction of graphene, nano-carbon, etc., can solve the problems of low packing density of graphene powder, limited dispersion ability, and high energy consumption

Active Publication Date: 2014-07-09
安徽百特新材料科技有限公司
View PDF9 Cites 78 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Such a preparation process not only has high energy consumption and lengthy process flow; moreover, the packing density of the prepared graphene powder is extremely small, and the dispersion ability of the powder product in a sol

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
  • Method for preparing graphene through large-scale aqueous phase
  • Method for preparing graphene through large-scale aqueous phase
  • Method for preparing graphene through large-scale aqueous phase

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0046] The preparation process of the present invention includes the following steps:

[0047] (1) Using flake graphite powder, natural graphite powder, synthetic graphite powder or expanded graphite powder as starting materials, intercalation is carried out by oxidation intercalation method to prepare intercalated graphite;

[0048] The oxidant of the oxidation intercalation method described in step (1) can be sulfuric acid, nitric acid, perchloric acid, phosphoric acid, hydrogen peroxide, potassium permanganate, potassium dichromate, chromium trioxide, ammonium persulfate, formic acid, acetic acid, oxalic acid , Bromine, chlorine, iodine chloride, iodine bromide, ozone, oxygen, or any combination between them. , But not limited to this.

[0049] The preparation process of intercalated graphite described in step (1) refers to completion at low temperature, and the purpose is to avoid excessive oxidation of the graphene sheet during the intercalation process. The preferred interca...

Embodiment 1

[0064] Mix 200 ml of concentrated sulfuric acid (98%) with 10 g of potassium permanganate (purity> 95%), 10 grams of flake graphite powder (particle diameter is 500 microns or 35 mesh, carbon content> 95%) uniform mixing, control system temperature below 35 o C. After stirring continuously for 1 hour, slowly add it to 500 ml of ice water, taking care to remove the heat of mixing in time to avoid excessively high system temperature. Then add 20 ml of hydrogen peroxide and stir for 5 minutes, and obtain sulfuric acid intercalated graphite intercalation compound after filtration.

[0065] The sulfuric acid-graphite intercalation compound (wet) obtained after filtration was mixed with 10 g of sodium hydroxide and 250 ml of water. An ultrasonic probe (power 500 W, 95%) was used to obtain a black graphene suspension after 10 minutes. After centrifuging the resulting black solution for 10 minutes at 10,000 revolutions / min, the supernatant was poured to obtain an aqueous paste with high ...

Embodiment 2

[0068] Mix 100 milliliters of fuming sulfuric acid (containing 20% ​​sulfur trioxide), 5 milliliters of hydrogen peroxide, and 10 grams of flake graphite powder (particle diameter of 500 microns) evenly, and pay attention to control the temperature of the system below 35 o C. After stirring continuously for 1 hour, filter, then add to oxalic acid solution and soak for 1 hour, and filter again to obtain intercalated graphite intercalation compound.

[0069] The sulfuric acid-graphite intercalation compound (wet) obtained after filtration was mixed with 10 g of sodium hydroxide and 250 ml of water. A black graphene suspension was obtained after 10 minutes with an ultrasonic probe (power 500W, 95%). After centrifuging the resulting black solution for 10 minutes at 10,000 rpm, the supernatant was poured to obtain an aqueous paste with high graphene content. Compared with graphite raw materials, the yield of graphene is greater than 90%.

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

PropertyMeasurementUnit
Diameteraaaaaaaaaa
Conductivityaaaaaaaaaa
Thicknessaaaaaaaaaa
Login to view more

Abstract

The invention provides a method for preparing graphene through a large-scale aqueous phase. According to the method, graphite serves as a raw material. The method comprises the following steps: intercalating the graphite by adopting an intercalator, so that interlayer spacing between graphene sheet layers is enlarged, and the interaction force between the layers is weakened; and directly treating the intercalated graphite through ultrasonic waves, stripping and uniformly dispersing the graphite in an alkaline aqueous solution with the pH value of 10-14, wherein the content of graphene in the dispersion can be over 100mg/mL (about 10 weight percent of graphene), the content of single-layer graphene in the aqueous phase dispersion is more than 90 percent, the equivalent diameter of the graphene sheet layers can be over 1-10 microns, and a graphene film formed by filtering has a complete lattice structure and high electric conductivity. The prepared high-concentration aqueous phase graphene paste can be stored for a long time and is convenient to transport and use. The method is simple in process flow, high in production efficiency, low in energy consumption and low in cost, a commercially available low-cost reagent is adopted, the reagent is easy to recover, and the production process is environment-friendly and pollution-free.

Description

Technical field [0001] The invention belongs to the technical field of graphene preparation, and relates to a method for preparing graphene in a large-scale aqueous phase, in particular to a method for achieving low energy consumption, high yield and large-scale graphene preparation through liquid phase exfoliated graphite technology. Background technique [0002] Graphene is the basic structural unit of natural graphite, with a thickness of only 0.335 nm. It has high mechanical modulus (1.0 TPa), thermal conductivity (5300 W / m.K), and specific surface area (2630 m). 2 / g) and charge mobility (250,000 cm 2 / V.s), has broad application prospects in polymer composite materials, energy materials, electronic communications and other fields. In order to realize the commercial application of graphene, the establishment of a low-cost, high-yield method for preparing high-quality graphene is a necessary prerequisite, which is also a key challenge faced by many current research work. Grap...

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
IPC IPC(8): C01B31/04C01B32/19
Inventor 卢红斌董雷林珊
Owner 安徽百特新材料科技有限公司
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