CN102167314B - Method for preparing graphene - Google Patents
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- CN102167314B CN102167314B CN 201110132705 CN201110132705A CN102167314B CN 102167314 B CN102167314 B CN 102167314B CN 201110132705 CN201110132705 CN 201110132705 CN 201110132705 A CN201110132705 A CN 201110132705A CN 102167314 B CN102167314 B CN 102167314B
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 86
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 50
- 238000000034 method Methods 0.000 title abstract description 14
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 43
- 239000010439 graphite Substances 0.000 claims abstract description 43
- 238000001291 vacuum drying Methods 0.000 claims abstract description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910021382 natural graphite Inorganic materials 0.000 claims abstract description 10
- 239000012286 potassium permanganate Substances 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 9
- 238000005406 washing Methods 0.000 claims abstract description 9
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims abstract description 8
- 238000003756 stirring Methods 0.000 claims abstract description 8
- 238000001132 ultrasonic dispersion Methods 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 238000002360 preparation method Methods 0.000 claims description 17
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 claims description 16
- 239000008367 deionised water Substances 0.000 claims description 10
- 229910021641 deionized water Inorganic materials 0.000 claims description 10
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical group [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 8
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 8
- 150000002823 nitrates Chemical class 0.000 claims description 7
- 239000004159 Potassium persulphate Substances 0.000 claims description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 5
- 235000019394 potassium persulphate Nutrition 0.000 claims description 5
- 235000010344 sodium nitrate Nutrition 0.000 claims description 5
- 239000004317 sodium nitrate Substances 0.000 claims description 5
- 229940001516 sodium nitrate Drugs 0.000 claims description 5
- 238000000967 suction filtration Methods 0.000 claims description 5
- 238000010792 warming Methods 0.000 claims description 5
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 3
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical group NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004160 Ammonium persulphate Substances 0.000 claims description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 2
- 235000019395 ammonium persulphate Nutrition 0.000 claims description 2
- 238000010790 dilution Methods 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 2
- 235000010333 potassium nitrate Nutrition 0.000 claims description 2
- 239000004323 potassium nitrate Substances 0.000 claims description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims description 2
- -1 terepthaloyl moietie Chemical compound 0.000 claims description 2
- 238000009776 industrial production Methods 0.000 abstract description 5
- 239000002904 solvent Substances 0.000 abstract description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 4
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 abstract 2
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 description 10
- 230000002829 reductive effect Effects 0.000 description 10
- 230000005540 biological transmission Effects 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 3
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000002389 environmental scanning electron microscopy Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000001311 chemical methods and process Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000005826 halohydrocarbons Chemical class 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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Abstract
The invention discloses a method for preparing graphene. The method comprises the following steps of: adding natural graphite, persulfate and phosphorus pentoxide into concentrated sulfuric acid, and reacting with stirring to obtain pre-oxidated graphite; adding pre-oxidated graphite, nitrate and potassium permanganate into concentrated sulfuric acid sequentially and reacting to obtain graphite oxide; and dissolving the graphite oxide in alcohol to prepare solution, performing ultrasonic dispersion, reacting in the sealed environment at the temperature of between 120 and 220 DEG C for 4 to 48houhrs, and then performing centrifugal washing until the pH is 6.5 to 7.5, and performing vacuum drying to obtain black graphene powder. No reducing agent is adopted in the method, the reducing capacity of a solvent is used to reduce the graphite oxide, and the method has the advantages of low cost, and light pollution, and is suitable for large-scale industrial production.
Description
Technical field
The present invention relates to the preparation field of Graphene, be specifically related to a kind of pure thermal reduction preparation method of Graphene.
Background technology
Graphene (graphene) is owing to have unique two dimensional crystal structure; High electronic conductivity, high thermal conductivity and high physical strength and high chemicalstability; In a lot of fields, have broad application prospects like fields such as photoelectron, magnetic energy, energy storage, catalysis.Since 2004 are found first, more and more receive the attention of scientific circles, cause the climax of research Graphene in the world, find that the earliest two scientists of Graphene obtain the Nobel Prize in physics in 2010 years.
The method for preparing at present Graphene has mechanically peel method, chemical Vapor deposition process and solution chemistry method.Mechanically peel method and chemical Vapor deposition process are not suitable for heavy industrialization and use because rate ratio is lower.The scale operation Graphene generally adopts the solution chemistry method, promptly earlier the natural graphite oxidation is prepared graphite oxide (graphene oxide), again graphite oxide is reduced into Graphene.Under liquid-phase condition, generally adopt Hydrazine Hydrate 80, NaBH
4Or KBH
4Deng reductive agent graphite oxide is reduced.Because this type reductive agent price is higher, and can pollute, and also is not suitable for large-scale industrial production.
For quality and the need of industrial production of taking into account Graphene; Software engineering researchers invent many new preparing methods; As disclosing a kind of preparation method of graphene among the Chinese patent ZL200910077131.9: with sodium Metal 99.5 and halohydrocarbon is raw material, through under inert environments, in solvent, carrying out the prepared in reaction Graphene.A kind of preparation method of graphene is disclosed among the Chinese patent ZL200810113596.0; This method is to adopt process for preparing graphenes by chemical vapour deposition; Comprise: the substrate that will have catalyzer is put into the reactor drum of anaerobic; Make substrate temperature reach 500～1200 ℃, in said reactor drum, feed carbonaceousmaterial then, obtain Graphene; Wherein, said catalyzer is metal or metallic compound.
Summary of the invention
The invention provides a kind of pure thermal reduction preparation method of Graphene, this method does not adopt any reductive agent, but utilizes the reducing power of solvent self to come reduction-oxidation graphite, and it is low to have a cost, pollutes fewly, is fit to the advantage of large-scale industrial production.
A kind of preparation method of graphene comprises step:
1) natural graphite, persulphate and Vanadium Pentoxide in FLAKES are joined in the vitriol oil; Adding deionized water 60 ℃～90 ℃ stirrings while stirring after 4 hours～10 hours makes it be cooled to 20 ℃～28 ℃; Gained suspension-s cleans to pH=6.5～7.5 with the deionized water suction filtration; Through vacuum-drying, obtain preoxidation graphite;
2) the preoxidation graphite, nitrate salt and the potassium permanganate that step 1) are obtained join in the vitriol oil successively; Ice bath stirred 1 hour～3 hours down; Be warming up to 30 ℃～40 ℃ again and stirred 2 hours～4 hours, add 60 ℃～80 ℃ warm water then, and temperature is risen to 70 ℃～100 ℃ and kept 10 minutes～40 minutes; With 60 ℃～80 ℃ warm water dilution, add H more successively at last
2O
2And Hydrogen chloride, and solution centrifugal washed to pH=6.5～7.5, through vacuum-drying, obtain graphite oxide;
3) graphite oxide be dissolved in be configured to solution in the alcohol, through behind the ultra-sonic dispersion in sealed environment in 120 ℃～220 ℃ reactions 4 hours～48 hours down, centrifuge washing to pH=6.5～7.5 through vacuum-drying, obtain the graphene powder of black then.
In order to reach better invention effect, preferably:
In the step 1), described persulphate is selected Sodium Persulfate, Potassium Persulphate or ammonium persulphate for use.
In the step 1), the mass ratio of described natural graphite, persulphate, Vanadium Pentoxide in FLAKES and the vitriol oil is 1: 1～3: 1～3: 10～30.Wherein, natural graphite is as raw material, and persulphate and Vanadium Pentoxide in FLAKES are as oxygenant, and the adding of the vitriol oil is the oxidation capacity of enhanced oxidation agent further.
Step 2) in, described nitrate salt is selected SODIUMNITRATE or saltpetre for use.
Step 2) in, the mass ratio of described preoxidation graphite, nitrate salt, potassium permanganate and the vitriol oil is 1: 1～3: 2～6: 20～50.Wherein, preoxidation graphite is as raw material, and nitrate salt and potassium permanganate are as oxygenant, and the adding of the vitriol oil is the oxidation capacity of enhanced oxidation agent further.
Temperature is being risen to described warm water and step 2 before 70 ℃～100 ℃ steps) described in the volume ratio of the vitriol oil be 1.9: 1～4: 1.
Described warm water and step 2 after temperature being risen to 70 ℃～100 ℃ steps) described in the volume ratio of the vitriol oil be 4: 1～8: 1.
Described H
2O
2(ydrogen peroxide 50) is used for some high price mn ions are reduced into soluble divalent manganesetion, and the preferred mass percentage concentration is the H of 10%-40%
2O
2
Described Hydrogen chloride is some metals or oxide precipitation dissolving just, and the preferred mass percentage concentration is the Hydrogen chloride of 3%-10%.
In the step 3), described alcohol is methyl alcohol, ethanol, n-propyl alcohol, Virahol, terepthaloyl moietie, propyl carbinol or isopropylcarbinol.
Consider the solubleness of graphite oxide in alcohol to avoid unnecessary waste, the concentration of graphite oxide is 0.1mg/mL～1mg/mL in the described solution.
Described vacuum-drying is 60 ℃～80 ℃ vacuum-dryings 6 hours～12 hours.
The described vitriol oil refers to that concentration expressed in percentage by weight more than or equal to 70% sulfuric acid, has implication sanctified by usage in this area.
Compared with prior art, the present invention has the following advantages:
1), the preparation of graphite oxide of the present invention carries out in two steps, promptly carry out preoxidation earlier and carry out deep oxidation again, in this way the graphite oxide oxidation of preparation get more fully, more thorough, more be prone in solvent, disperseed, for follow-up abundant reduction creates conditions.
2), the reduction of graphite oxide of the present invention adopts pure hot method, reduction-oxidation graphite need not any reductive agent such as Hydrazine Hydrate 80, NaBH in this way
4Or KBH
4, and utilize the reduction characteristic of solvent (alcohols) self to come reduction-oxidation graphite, the alcohols price of use is lower, so suitable low-cost, the large-scale industrial production of the present invention, and can reduce pollution.
Description of drawings
Fig. 1 is the X ray diffracting spectrum of embodiment 1 gained Graphene.
Fig. 2 is the stereoscan photograph of embodiment 1 gained Graphene.
Fig. 3 is the transmission electron microscope photo of embodiment 1 gained Graphene.
Fig. 4 is the X ray diffracting spectrum of embodiment 2 gained Graphenes.
Fig. 5 is the stereoscan photograph of embodiment 2 gained Graphenes.
Fig. 6 is the transmission electron microscope photo of embodiment 2 gained Graphenes.
Fig. 7 is the X ray diffracting spectrum of embodiment 3 gained Graphenes.
Fig. 8 is the stereoscan photograph of embodiment 3 gained Graphenes.
Fig. 9 is the transmission electron microscope photo of embodiment 3 gained Graphenes.
Embodiment
Embodiment 1
1), with 5 gram Potassium Persulphate; It is in 98% the vitriol oil (71.8g) that 5 gram Vanadium Pentoxide in FLAKESs and 5 gram natural graphite powders join 39 milliliters of mass percentage concentration; Stirred 6 hours at 80 ℃ of lower magnetic forces; Add deionized water then while stirring and make it be cooled to room temperature, suspension-s cleans to pH=7 with the deionized water suction filtration, obtains 5.3 gram preoxidation graphite in 10 hours 60 ℃ of following vacuum-dryings again;
2), with 2 gram preoxidation graphite; 2 gram SODIUMNITRATE, it is in 98% the vitriol oil (84.6g) that 6 gram potassium permanganate join 46 milliliters of mass percentage concentration, ice bath stirred 1 hour down; Being warming up to 35 ℃ again stirred 2 hours; The warm water that adds 90 milliliters 70 ℃ then, and temperature risen to 98 ℃ and kept 15 minutes then adds 280 milliliters 70 ℃ warm water, 10 milliliters of mass percentage concentration and is 30% H successively
2O
2And 24 milliliters of mass percentage concentration are 5% Hydrogen chloride, to pH=7, and obtain the 4.3g graphite oxide in 10 hours 60 ℃ of following vacuum-dryings through abundant centrifuge washing;
3), the 0.05g graphite oxide is dissolved in the solution that is configured to 0.5mg/mL in the ethanol; Through in autoclave, reacting 24 hours down behind the ultra-sonic dispersion in 200 ℃; After the cooling with the throw out centrifuge washing to pH=7, and obtained the graphene powder of 0.021g black in 10 hours 60 ℃ of following vacuum-dryings.
Adopt X ray polycrystalline diffractometer that the final reacting product of gained is carried out material phase analysis; X ray diffracting spectrum (XRD figure spectrum) is like Fig. 1; Can find out from Fig. 1: through pure thermal response, graphite oxide has been reduced into Graphene, is characterized as (002) diffraction peak that occurs about 25 degree.
Adopt ESEM and transmission electron microscope that the final reacting product of gained is analyzed, its stereoscan photograph and transmission electron microscope photo can be found out from Fig. 2 and Fig. 3 respectively like Fig. 2 and Fig. 3: through pure thermal response, formed laminar ground Graphene.
Embodiment 2
1), with 15 gram Potassium Persulphate; It is in 90% the vitriol oil that 15 gram Vanadium Pentoxide in FLAKESs and 5 gram natural graphite powders join the 150g mass percentage concentration; Stirred 4 hours at 90 ℃ of lower magnetic forces; Add deionized water then while stirring and make it be cooled to 28 ℃, suspension-s cleans to pH=6.5 with the deionized water suction filtration, obtains 5.5g preoxidation graphite in 6 hours 80 ℃ of following vacuum-dryings again;
2), with 2 gram preoxidation graphite; 6 gram SODIUMNITRATE, it is in 98% the vitriol oil that 4 gram potassium permanganate join the 40g mass percentage concentration, ice bath stirred 3 hours down; Being warming up to 30 ℃ again stirred 4 hours; The warm water that adds 90 milliliters 60 ℃ then, and temperature risen to 70 ℃ and kept 40 minutes then adds 280 milliliters 60 ℃ warm water, 10 milliliters of mass percentage concentration and is 10% H successively
2O
2And 24 milliliters of mass percentage concentration are 10% Hydrogen chloride, to pH=6.5, and obtain the 4.5g graphite oxide in 6 hours 80 ℃ of following vacuum-dryings through abundant centrifuge washing;
3), the 0.01g graphite oxide is dissolved in the solution that is configured to 0.1mg/mL in the Virahol; Through in autoclave, reacting 48 hours down behind the ultra-sonic dispersion in 120 ℃; After the cooling with the throw out centrifuge washing to pH=6.5, and obtained the graphene powder of 0.004g black in 6 hours 80 ℃ of following vacuum-dryings.
Adopt X ray polycrystalline diffractometer that the final reacting product of gained is carried out material phase analysis, the XRD figure spectrum shows like Fig. 4: through pure thermal response, graphite oxide has been reduced into Graphene, is characterized as (002) diffraction peak that occurs about 25 degree.
Adopt ESEM and transmission electron microscope that the final reacting product of gained is analyzed, its stereoscan photograph such as Fig. 5 and transmission electron microscope photo such as Fig. 6 show: through pure thermal response, formed laminar ground Graphene.
Embodiment 3
1), with 10 gram Potassium Persulphate; It is in 70% the vitriol oil that 10 gram Vanadium Pentoxide in FLAKESs and 5 gram natural graphite powders join the 50g mass percentage concentration; Stirred 10 hours at 60 ℃ of lower magnetic forces; Add deionized water then while stirring and make it be cooled to 20 ℃, suspension-s cleans to pH=7.5 with the deionized water suction filtration, obtains 5.2g preoxidation graphite in 12 hours 70 ℃ of following vacuum-dryings again;
2), with 2 gram preoxidation graphite; 4 gram SODIUMNITRATE, it is in 98% the vitriol oil that 12 gram potassium permanganate join the 100g mass percentage concentration, ice bath stirred 2 hours down; Being warming up to 40 ℃ again stirred 3 hours; The warm water that adds 400 milliliters 80 ℃ then, and temperature risen to 100 ℃ and kept 10 minutes then adds 400 milliliters 80 ℃ warm water, 10 milliliters of mass percentage concentration and is 40% H successively
2O
2And 24 milliliters of mass percentage concentration are 3% Hydrogen chloride, to pH=7.5, and obtain the 4.7g graphite oxide in 12 hours 70 ℃ of following vacuum-dryings through abundant centrifuge washing;
3), the 0.1g graphite oxide is dissolved in the solution that is configured to 1mg/mL in the methyl alcohol; Through in autoclave, reacting 4 hours down behind the ultra-sonic dispersion in 220 ℃; After the cooling with the throw out centrifuge washing to pH=7.5, and obtained the graphene powder of 0.046g black in 12 hours 70 ℃ of following vacuum-dryings.
Adopt X ray polycrystalline diffractometer that the final reacting product of gained is carried out material phase analysis, the XRD figure spectrum shows like Fig. 7: through pure thermal response, graphite oxide has been reduced into Graphene, is characterized as (002) diffraction peak that occurs about 25 degree.
Adopt ESEM and transmission electron microscope that the final reacting product of gained is analyzed, its stereoscan photograph such as Fig. 8 and transmission electron microscope photo such as Fig. 9 show:: through pure thermal response, formed laminar ground Graphene.
Claims (8)
1. a preparation method of graphene is characterized in that, comprises step:
1) natural graphite, persulphate and Vanadium Pentoxide in FLAKES are joined in the vitriol oil; Adding deionized water 60 ℃～90 ℃ stirrings while stirring after 4 hours～10 hours makes it be cooled to 20 ℃～28 ℃; Gained suspension-s cleans to pH=6.5～7.5 with the deionized water suction filtration; Through vacuum-drying, obtain preoxidation graphite;
2) the preoxidation graphite, nitrate salt and the potassium permanganate that step 1) are obtained join in the vitriol oil successively; Ice bath stirred 1 hour～3 hours down; Be warming up to 30 ℃～40 ℃ again and stirred 2 hours～4 hours, add 60 ℃～80 ℃ warm water then, and temperature is risen to 70 ℃～100 ℃ and kept 10 minutes～40 minutes; With 60 ℃～80 ℃ warm water dilution, add H more successively at last
2O
2And Hydrogen chloride, and solution centrifugal washed to pH=6.5～7.5, through vacuum-drying, obtain graphite oxide;
3) graphite oxide is dissolved in is configured to the solution that graphite oxide concentration is 0.1mg/mL～1mg/mL in the alcohol; Through in sealed environment, reacting 4 hours～48 hours down behind the ultra-sonic dispersion in 120 ℃～220 ℃; Centrifuge washing is to pH=6.5～7.5 then; Through vacuum-drying, obtain the graphene powder of black;
In the step 1), the mass ratio of described natural graphite, persulphate, Vanadium Pentoxide in FLAKES and the vitriol oil is 1:1～3:1～3:10～30;
Step 2) in, the mass ratio of described preoxidation graphite, nitrate salt, potassium permanganate and the vitriol oil is 1:1～3:2～6:20～50.
2. preparation method of graphene according to claim 1 is characterized in that, in the step 1), described persulphate is Sodium Persulfate, Potassium Persulphate or ammonium persulphate.
3. preparation method of graphene according to claim 1 is characterized in that step 2) in, described nitrate salt is SODIUMNITRATE or saltpetre.
4. preparation method of graphene according to claim 1 is characterized in that, temperature is being risen to described warm water and step 2 before 70 ℃～100 ℃ steps) described in the volume ratio of the vitriol oil be 1.9:1～4:1.
5. preparation method of graphene according to claim 1 is characterized in that, described warm water and step 2 after temperature being risen to 70 ℃～100 ℃ steps) described in the volume ratio of the vitriol oil be 4:1～8:1.
6. preparation method of graphene according to claim 1 is characterized in that, in the step 3), described alcohol is methyl alcohol, ethanol, n-propyl alcohol, Virahol, terepthaloyl moietie, propyl carbinol or isopropylcarbinol.
7. preparation method of graphene according to claim 1 is characterized in that, described vacuum-drying is 60 ℃～80 ℃ vacuum-dryings 6 hours～12 hours.
8. preparation method of graphene according to claim 1 is characterized in that the concentration expressed in percentage by weight of the described vitriol oil is at least 70%;
Described H
2O
2Mass percentage concentration be 10%-40%;
The mass percentage concentration of described Hydrogen chloride is 3%-10%.
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| CN102504145B (en) * | 2011-11-15 | 2013-11-13 | 苏州大学 | Preparation method for polymer grafted graphene oxide |
| CN103159208A (en) * | 2011-12-14 | 2013-06-19 | 海洋王照明科技股份有限公司 | Preparation method of graphene |
| CN102557018B (en) * | 2011-12-16 | 2015-07-29 | 中国热带农业科学院农产品加工研究所 | A kind of based on green deoxidation technology graphene preparation method |
| CN102583343B (en) * | 2012-02-08 | 2016-01-13 | 中国科学院福建物质结构研究所 | A kind of method preparing Graphene in enormous quantities |
| CN103359712A (en) * | 2012-03-29 | 2013-10-23 | 海洋王照明科技股份有限公司 | Graphite oxide/graphene oxide composite material, preparation method thereof, battery anode and capacitor battery |
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| CN103771397A (en) * | 2012-10-23 | 2014-05-07 | 海洋王照明科技股份有限公司 | Preparation method for graphene and super capacitor |
| CN103848419B (en) * | 2013-12-10 | 2016-08-31 | 南京工业大学 | Method for preparing ultrafine graphite oxide by membrane process washing separation |
| CN103950926B (en) * | 2014-05-14 | 2016-02-10 | 石家庄铁道大学 | A kind of method preparing single-layer graphene fast |
| CN104051160A (en) * | 2014-05-30 | 2014-09-17 | 大英聚能科技发展有限公司 | Graphene for electrical double-layer capacitor and preparation method thereof |
| CN105645384A (en) * | 2014-12-02 | 2016-06-08 | 中国科学院过程工程研究所 | Preparation method of graphene |
| CN106744895A (en) * | 2016-12-28 | 2017-05-31 | 江苏中亚新材料股份有限公司 | A kind of preparation method of high-purity multi-layer graphene |
| CN109135686B (en) * | 2018-08-10 | 2020-01-21 | 中国矿业大学 | Graphene-based modified nano fluid heat transfer working medium and preparation method thereof |
| CN109012587B (en) * | 2018-08-21 | 2021-03-23 | 齐鲁工业大学 | Preparation method of tetracycline hydrophilic carbon composite adsorbent |
| CN113481648B (en) * | 2021-07-02 | 2022-11-29 | 福建天守纺织新材料有限公司 | Sweat-releasing antibacterial skin-friendly fabric and preparation method thereof |
| CN114588887A (en) * | 2022-03-07 | 2022-06-07 | 厦门理工学院 | Z-shaped composite photocatalyst and preparation method thereof |
| CN115845805B (en) * | 2022-11-18 | 2024-07-09 | 哈尔滨工业大学（深圳） | Preparation method of nitrogen-doped Fe-BTC derived carbon-based material of activated peroxymonosulfate |
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| CN101966988B (en) * | 2010-11-17 | 2012-07-04 | 哈尔滨工业大学 | Method for preparing graphene powder |
| CN102001651B (en) * | 2010-12-30 | 2012-08-22 | 上海交通大学 | Method for preparing graphene based on hydroxylamine reduction |
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| C. Nethravathi et al..Chemically modified graphene sheets produced by the solvothermal reduction of colloidal dispersions of graphite oxide.《Carbon》.2008,第46卷1994-1998. * |
| Nina I. Kovtyukhova et al..Layer-by-Layer Assembly of Ultrathin Composite Films from Micron-Sized Graphite Oxide Sheets and Polycations.《Chem. Mater.》.1999,第11卷(第3期),771-778. * |
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