CN105819438B - A kind of method using aquashear prepare with scale nano-graphene material - Google Patents
A kind of method using aquashear prepare with scale nano-graphene material Download PDFInfo
- Publication number
- CN105819438B CN105819438B CN201610295055.9A CN201610295055A CN105819438B CN 105819438 B CN105819438 B CN 105819438B CN 201610295055 A CN201610295055 A CN 201610295055A CN 105819438 B CN105819438 B CN 105819438B
- Authority
- CN
- China
- Prior art keywords
- graphene
- graphite
- prepare
- nano
- aquashear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 98
- 239000000463 material Substances 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims abstract description 31
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 119
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 47
- 239000010439 graphite Substances 0.000 claims abstract description 47
- 239000007788 liquid Substances 0.000 claims abstract description 25
- 238000000227 grinding Methods 0.000 claims abstract description 14
- 238000009826 distribution Methods 0.000 claims abstract description 13
- 239000007800 oxidant agent Substances 0.000 claims abstract description 8
- 230000001590 oxidative effect Effects 0.000 claims abstract description 7
- 230000001804 emulsifying effect Effects 0.000 claims abstract description 6
- 239000012530 fluid Substances 0.000 claims abstract description 3
- 239000006185 dispersion Substances 0.000 claims description 32
- 238000002156 mixing Methods 0.000 claims description 21
- 239000000725 suspension Substances 0.000 claims description 18
- 238000010008 shearing Methods 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical group [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 4
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 claims description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 4
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 claims description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 2
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 claims description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 2
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 claims description 2
- WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 0.000 claims description 2
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- 229960000583 acetic acid Drugs 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- SIXOAUAWLZKQKX-UHFFFAOYSA-N carbonic acid;prop-1-ene Chemical compound CC=C.OC(O)=O SIXOAUAWLZKQKX-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229940117975 chromium trioxide Drugs 0.000 claims description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 2
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 claims description 2
- 239000008367 deionised water Substances 0.000 claims description 2
- 229910021641 deionized water Inorganic materials 0.000 claims description 2
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims description 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 2
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 claims description 2
- 238000004945 emulsification Methods 0.000 claims description 2
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 2
- 239000012362 glacial acetic acid Substances 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical group CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 claims description 2
- 239000012286 potassium permanganate Substances 0.000 claims description 2
- UMPKMCDVBZFQOK-UHFFFAOYSA-N potassium;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[K+].[Fe+3] UMPKMCDVBZFQOK-UHFFFAOYSA-N 0.000 claims description 2
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims 2
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 claims 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 1
- -1 graphite Alkene Chemical class 0.000 claims 1
- 150000004040 pyrrolidinones Chemical class 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract description 2
- 208000027418 Wounds and injury Diseases 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract description 2
- 208000014674 injury Diseases 0.000 abstract description 2
- 229910052744 lithium Inorganic materials 0.000 abstract description 2
- 239000003973 paint Substances 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 230000005855 radiation Effects 0.000 abstract description 2
- 230000000694 effects Effects 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 14
- 238000001914 filtration Methods 0.000 description 14
- 239000011591 potassium Substances 0.000 description 14
- 229910052700 potassium Inorganic materials 0.000 description 14
- 150000001336 alkenes Chemical class 0.000 description 9
- 239000004575 stone Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 238000003760 magnetic stirring Methods 0.000 description 7
- 238000003801 milling Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 239000003643 water by type Substances 0.000 description 7
- 238000010924 continuous production Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 238000000053 physical method Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- NJPQAIBZIHNJDO-UHFFFAOYSA-N 1-dodecylpyrrolidin-2-one Chemical class CCCCCCCCCCCCN1CCCC1=O NJPQAIBZIHNJDO-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 238000003421 catalytic decomposition reaction Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000000320 mechanical mixture Substances 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
Landscapes
- Carbon And Carbon Compounds (AREA)
Abstract
The present invention proposes a kind of method using aquashear prepare with scale nano-graphene material; graphite powder is added in liquid; add a small amount of oxidant; pass through multi-functional grinding distribution machine, high-shear emulsifying device, the high pressure homogenizer of series connection; oxidizer molecule quickly interts and enters inside graphite; material is peeled off in fluid power effect down cut using continuous mechanical force, make its fast hierarchical.Both solved and be difficult to extensive, high quality, low cost at present and prepare graphene, it in turn ensure that graphene-structured is injury-free, obtained graphene can be widely applied to the fields such as lithium battery, ultracapacitor, polymer composite, heat conduction and heat radiation film, functional paint, defence and military.
Description
Technical field
The present invention relates to technical field of nano material, relates generally to one kind and utilizes aquashear prepare with scale nano-graphite
The method of alkene material.
Background technology
Since grapheme material in 2004 is found, researcher has carried out it to further investigate for a long time, and from
The hexagonal structure that graphene is made of SP2 hybridized orbits is drawn in research, since the presence of SP2 hybridized orbits causes stone
Black alkene has good electric conductivity, can be applied as good conductor in opto-electronic device and electrochemical energy source domain.With
Deeply, the optical property of graphene, mechanical property, catalytic performance etc. are found in succession for research so that its electromagnetic shielding material,
The fields such as microwave absorbing material, gas sensor, catalyst are also widely used.
Graphene possesses excellent performance and is widely applied prospect, but the technology of preparing of graphene is not yet ripe, product
It is of low quality, performance is unstable and can not mass produce and all limits its extensive use in every field.Prepare at present
The preparation species of graphene is various, mainly there is two major class of physical method and chemical method, but more or less there are it is corresponding the problem of,
Lead to not the needs for meeting industrial mass production.Graphene prepared by physical method is mainly based on mechanical stripping, but produce
Moral character can be unstable, and Size Distribution can not be controlled accurately, and graphene size is to influence a key factor of its performance.
Advantage is that energy consumption is small, and pollution is small, and safety can large-scale continuous production.Chemical method prepare graphene mainly have catalytic decomposition and
The methods of organic synthesis, in addition can also notify graphite to carry out preparing grapheme through oxidation reduction.Graphene prepared by chemical method
It is controllable with size, steady performance, but energy consumption is larger in chemical method preparation process, unsuitable large-scale continuous production,
And there is higher danger compared with physical method.And a large amount of inorganic matters and soda acid can be used in preparation process, cause technique
Subsequent treatment is complex, also adds production cost indirectly;Oxidation in chemical process can cause the hydraulic performance decline of graphene.
Chinese invention patent application number 201310750433.4 discloses a kind of method for preparing super capacitor slurry, it is logical
Cross after graphene, binding agent, solvent and other auxiliary additives tentatively mixing, mixed liquor is carried out using high-shear emulsifying device
Mechanical mixture.The preferable graphene dispersing solution of dispersiveness can obtain by this method, and jitter time can be shortened.
Chinese invention patent application number 201510073825.0 discloses the class mechanical stripping of a kind of tonne of production graphene
Device and its production method, it is made of level-one or multi-stage mechanical peel-off device its mechanical stripping separator, passes through
Mutual collision between rotor and graphite, between graphite particle is peeled off, and realizes multistage continuous processing, can on a large scale, persistently
Property prepares graphene and its dispersion liquid.
Chinese invention patent application number 201511007072.X discloses a kind of method that graphene is prepared using lignin,
It is pre-processed by using acid-base pair lignin, is then mixed by high pressure homogenizer, homogeneous, and under the action of catalyst
Decompose, then graphene is prepared into pyrolytic is crossed.
Chinese invention patent application number 201010179119.1 discloses high-efficiency and low-cost mechanical stripping and prepares graphene
Or the method for graphene oxide, then it passes through machinery by the way that graphite is mixed in a solvent with other larger particles
Stripping prepares graphene.The charge stripping efficiency of graphite can be improved by this method, and can realize large-scale production.
From above-mentioned analysis it can be found that the method for preparing graphene using mechanical stripping at present is more, but these method bases
Originally it is all based on what a kind of mechanical stripping method carried out, obtained graphene is with quality is unstable, size is uneven, Wu Fa great
Some problems such as scale continuous production.The present invention is by the way that grinding distribution agent, high-shear emulsion machine, high pressure homogenizer are connected, stone
Black mixed liquor, which passes sequentially through three kinds of mechanical stripping devices, to be continued to peel off mixing repeatedly, be made be uniformly dispersed, size uniformity
Graphite.Both it ensure that shearing is peeled off, by ensure that graphene-structured is injury-free, obtained graphene can be widely applied to lithium
The fields such as battery, ultracapacitor, polymer composite, heat conduction and heat radiation film, functional paint, defence and military.
The content of the invention
For at present using mechanical stripping equipment can not prepare size uniform, be uniformly dispersed, stable quality graphene is asked
Topic, the present invention proposes to carry out stripping mixing to graphene using connect a variety of mechanical stripping equipments and mixing apparatus, to solve to work as
Before prepare graphene process problem encountered.Carry out lift-off processing step by step to graphite especially by fluid power and obtain nano-graphite
Alkene material, concrete technical scheme are as follows:
(1)Oxidant is dissolved in solvent, graphite dispersion is then formed into graphite powder mixed liquor into solution, graphite mixes
The concentration for closing liquid is 10-100g/L;
(2)By step(1)Obtained graphite powder mixed liquor is sent to progress first time grinding in grinding distribution machine, obtains one
The graphene suspension being sized;
(3)By step(2)In obtained graphene suspension continue to be fed into high-shear emulsifying device and carry out second of machinery
Shearing and mixing, obtain particle diameter smaller, the more preferable graphene dispersing solution of dispersiveness;
(4)By step(3)In obtained graphene dispersing solution continue to be fed into high pressure homogenizer, utilize high pressure homogenizer pair
Graphene dispersing solution mixes again, and then material is sprayed by high-pressure homogeneous machine nozzle occurs mutually collision, realizes third time machine
Tool is peeled off, and obtains the graphene dispersing solution of size uniform;
(5)By step(4)In obtained graphene dispersing solution filtered, centrifuged, is dry, obtain nano-graphene material
Material.
Preferably, the graphite raw material chooses natural flake graphite, graphite powder, expanded graphite, highly oriented graphite, unformed
One kind in carbon.
Preferably, the oxidant is ammonium persulfate, potassium bichromate, chromium trioxide, potassium permanganate, potassium ferrate, dense sulphur
Mixture more than one or both of acid, concentrated hydrochloric acid, concentrated nitric acid, perchloric acid, concentrated phosphoric acid or glacial acetic acid, graphite and oxidant
Dosage mass ratio is 1:0.1-0.3.
Preferably, the solvent is selected from butyl acetate, benzyl oxide, diethyl carbonate, DBE, ethyl carbitol acetate, carbonic acid
Methyl ethyl ester, butyl carbitol acetate, butyl cellosolve acetate, propene carbonate, monoethanolamine, DMSO, dimethyl succinate,
N- dodecyl pyrrolidones, propylene glycol methyl ether acetate, NMP, ethyl phthalate, dimethylbenzene, pyridine, phthalic acid two
Any of butyl ester, benzaldehyde, dimethyl carbonate, N- octylpyrrolidones, diphenyl carbonate and deionized water or two kinds
Combination above.
Preferably, the rotating speed of the mechanical lapping is 100-1500rpm, splitting time 1-5h.
Preferably, the shearing force of the high-shear emulsifying is 1000-5000ips, emulsification times 0.5-3h.
Preferably, the operating pressure higher than homogenizer is 10-80MPa.
It is proposed by the present invention that nanometer is prepared using multistage aquashear compared with the technology of existing preparation graphene microchip
Grapheme material has the advantage that:
It is 1. mixed present invention firstly provides carrying out repeatedly peeling off to graphene using a variety of aquashear equipment tandem compounds
Conjunction processing prepares nano-graphene material;
2. to be combined since present invention employs grinding distribution machine, high-shear emulsion machine, high pressure homogenizer, realize
The mixing of stripping step by step of graphene, obtained graphene size are more uniformly distributed, and oxidant progress is added due to during
Show to handle, graphene is less likely to occur to reunite;
3. since three devices of the present invention are in series, it is possible to achieve large-scale continuous production, and it is safe and pollution-free.
Brief description of the drawings
For further illustrate a kind of method using aquashear prepare with scale nano-graphene material, by attached drawing into
Row explanation.
A kind of flow chart using aquashear prepare with scale nano-graphene material of attached drawing 1.
Specific embodiment:
By embodiment, the present invention is described in further detail, but this should not be interpreted as to the model of the present invention
Enclose and be only limitted to following example.Without departing from the idea of the above method of the present invention, according to ordinary skill knowledge
The various replacements or change made with customary means, should be included in the scope of the present invention.
Embodiment 1
5g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
500rpm, milling time 2h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 2000ips, mechanical stripping disperses 0.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 2
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
500rpm, milling time 2h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 2000ips, mechanical stripping disperses 0.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 3
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
1000rpm, milling time 2h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 2000ips, mechanical stripping disperses 0.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 4
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
1000rpm, milling time 4h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 2000ips, mechanical stripping disperses 0.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 5
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
1000rpm, milling time 4h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 5000ips, mechanical stripping disperses 0.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 6
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
1000rpm, milling time 3h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 5000ips, mechanical stripping disperses 1.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 50MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Embodiment 7
10g potassium ferrates are weighed, are dissolved in 1L deionized waters, then weigh 50g graphite powders, by itself and high ferro
Sour potassium solution is tentatively mixed under magnetic stirring, obtains graphite mixed liquor;
By stepIn graphite mixed liquor be injected into grinding distribution machine and carry out first time mechanical stripping, rotating speed is
1000rpm, milling time 4h;Obtain the larger graphene suspension of grain size;
By stepGraphene suspension made from middle process first time mechanical stripping is sent directly into height by pipeline and cuts
Cut in emulsifier, in the case where shearing force is 5000ips, mechanical stripping disperses 1.5h, obtains smaller, the scattered stone being more uniformly distributed
Black alkene dispersion liquid;
By stepThe middle graphene dispersion being mixed to prepare by second of mechanical stripping is sent directly into height by pipeline
Press in homogenizer, pressurization mixing is carried out to material, after 80MPa is reached, material is by the nozzle of high pressure homogenizer with higher
Speed sprays head-on collision, realizes that third time peels off mixing;
By stepObtained dispersion liquid carries out filtration treatment, removes larger-size graphene particles in dispersion liquid,
The product cut size made is more uniformly distributed;
By stepGraphene dispersing solution obtained by middle filtering is centrifuged, drying process, obtains nano-graphene material
Material.
Claims (2)
- A kind of 1. method using aquashear prepare with scale nano-graphene material, it is characterised in that by difference in functionality Mechanical stripping equipment is connected, and is carried out lift-off processing step by step to graphite by fluid power and is obtained nano-graphene material, specific side Method is as follows:(1)Oxidant is dissolved in solvent, graphite dispersion is then formed into graphite powder mixed liquor, graphite mixed liquor into solution Concentration be 10-100g/L;The oxidant is ammonium persulfate, potassium bichromate, chromium trioxide, potassium permanganate, potassium ferrate, dense Mixture more than one or both of sulfuric acid, concentrated hydrochloric acid, concentrated nitric acid, perchloric acid, concentrated phosphoric acid or glacial acetic acid, graphite and oxidation Agent dosage mass ratio is 1:0.1-0.3;The solvent is selected from butyl acetate, benzyl oxide, diethyl carbonate, DBE, ethyl carbitol acetate, methyl ethyl carbonate, fourth Base carbitol acetate, butyl cellosolve acetate, propene carbonate, monoethanolamine, DMSO, dimethyl succinate, N- dodecanes Base pyrrolidones, propylene glycol methyl ether acetate, NMP, ethyl phthalate, dimethylbenzene, pyridine, dibutyl phthalate, rest in peace Any of fragrant aldehyde, dimethyl carbonate, n-octylpyrrolidone, diphenyl carbonate and deionized water or two or more groups Close;(2)By step(1)Obtained graphite powder mixed liquor is sent to progress first time grinding in grinding distribution machine, obtains a scale Very little graphene suspension;The rotating speed of the mechanical lapping is 100-1500rpm, splitting time 1-5h;(3)By step(2)In obtained graphene suspension continue to be fed into second of mechanical shearing carried out in high-shear emulsifying device And mixing, obtain particle diameter smaller, the more preferable graphene dispersing solution of dispersiveness;The shearing force of the high-shear emulsifying is 1000- 5000ips, emulsification times 0.5-3h;(4)By step(3)In obtained graphene dispersing solution continue to be fed into high pressure homogenizer, using high pressure homogenizer to graphite Alkene dispersion liquid mixes again, and then material is sprayed by high-pressure homogeneous machine nozzle occurs mutually collision, realizes third time machinery stripping From obtaining the graphene dispersing solution of size uniform;The operating pressure of the high pressure homogenizer is 10-80MPa;(5)By step(4)In obtained graphene dispersing solution filtered, centrifuged, is dry, obtain nano-graphene material.
- 2. a kind of method using aquashear prepare with scale nano-graphene material according to claim 1, its feature It is, the graphite raw material chooses one in natural flake graphite, graphite powder, expanded graphite, highly oriented graphite, agraphitic carbon Kind.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610295055.9A CN105819438B (en) | 2016-05-06 | 2016-05-06 | A kind of method using aquashear prepare with scale nano-graphene material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610295055.9A CN105819438B (en) | 2016-05-06 | 2016-05-06 | A kind of method using aquashear prepare with scale nano-graphene material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN105819438A CN105819438A (en) | 2016-08-03 |
| CN105819438B true CN105819438B (en) | 2018-04-17 |
Family
ID=56528207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610295055.9A Active CN105819438B (en) | 2016-05-06 | 2016-05-06 | A kind of method using aquashear prepare with scale nano-graphene material |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105819438B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20220289576A1 (en) * | 2019-07-09 | 2022-09-15 | Applied Graphene Materials Uk Limited | Dispersions |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106276857B (en) | 2016-08-12 | 2018-06-26 | 上海交通大学 | A kind of method for preparing functional carbon material |
| TWI668187B (en) * | 2016-10-07 | 2019-08-11 | 林逸樵 | Device for rapidly producing graphene and method thereof |
| TWI668188B (en) * | 2016-10-07 | 2019-08-11 | 林逸樵 | Device and method for rapidly producing graphene/nano metal oxide composite material |
| CN106607125B (en) * | 2016-12-27 | 2018-11-09 | 成都新柯力化工科技有限公司 | A method of the homogenizer and its stripping graphene of stripping graphene |
| CN106542527B (en) * | 2017-01-06 | 2017-12-08 | 成都新柯力化工科技有限公司 | A kind of mechanical stripping grading system for graphene microchip dispersion liquid method |
| TWI625299B (en) * | 2017-01-24 | 2018-06-01 | Apparatus for producing graphene and method thereof | |
| CN108047822B (en) * | 2017-10-27 | 2019-09-03 | 广东烯谷碳源新材料有限公司 | Utilize the method for shear thickening system removing preparing graphite alkene heat conduction and heat radiation composite material |
| CN107814380B (en) * | 2017-10-27 | 2019-07-23 | 中南民族大学 | Utilize the method for shear thickening system removing preparing graphite alkene |
| CN107934941A (en) * | 2017-11-23 | 2018-04-20 | 安徽百特新材料科技有限公司 | A kind of preparation method of graphene |
| CN107934940A (en) * | 2017-11-23 | 2018-04-20 | 安徽百特新材料科技有限公司 | A kind of preparation facilities of graphene |
| TWI692441B (en) * | 2018-01-17 | 2020-05-01 | 中原大學 | Graphene structure, method of producing graphene and electrode of lithium-ion made of the same |
| CN108439390A (en) * | 2018-05-29 | 2018-08-24 | 武汉科技大学 | Based on the method for isolating and purifying graphene from Pintsch process charcoal |
| CN108862259B (en) * | 2018-08-13 | 2022-04-01 | 深圳天元羲王材料科技有限公司 | Graphene production method and device |
| CN109370370A (en) * | 2018-09-10 | 2019-02-22 | 成都紫苑华光新材料科技有限公司 | A kind of graphene exothermic paint and preparation method thereof |
| CN109052380A (en) * | 2018-09-10 | 2018-12-21 | 成都紫苑华光新材料科技有限公司 | The method that full liquid water phase physics removing prepares graphene |
| CN109346240B (en) * | 2018-09-10 | 2021-02-02 | 明德润和新材料(珠海)有限公司 | Preparation method of graphene conductive slurry |
| CN109192955A (en) * | 2018-09-10 | 2019-01-11 | 成都紫苑华光新材料科技有限公司 | A kind of preparation method of LiFePO4/graphene in-situ composite |
| CN110550623B (en) * | 2019-10-16 | 2022-07-29 | 燕山大学 | A method for large-scale preparation of high-quality large-scale graphene |
| CN110620237A (en) * | 2019-10-25 | 2019-12-27 | 新奥石墨烯技术有限公司 | Conductive paste, preparation method and application thereof, and battery |
| CN112694083B (en) * | 2021-02-01 | 2022-10-21 | 天津艾克凯胜石墨烯科技有限公司 | Method for continuously producing graphene quantum dot slurry on large scale |
| CN113213468B (en) * | 2021-05-31 | 2022-12-23 | 杭州高烯科技有限公司 | Equipment for preparing graphene oxide with uniform size by one-step method |
| CN113213469B (en) * | 2021-05-31 | 2022-12-23 | 杭州高烯科技有限公司 | Equipment for preparing uniform small-size graphene oxide |
| CN113690429B (en) * | 2021-08-23 | 2024-12-03 | 武汉立承科技有限公司 | Carbon-coated graphene/metal oxide composite material and preparation method thereof |
| CN115819000A (en) * | 2021-12-31 | 2023-03-21 | 南京诚赢集约建材科技有限公司 | Pilot test method based on mixed dispersion of asphalt regenerant and graphene |
| CN116332166A (en) * | 2023-03-23 | 2023-06-27 | 南通丝洛拉新材料科技有限公司 | A preparation method of single-layer transparent graphene and its application in antibacterial fiber |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103521330B (en) * | 2013-10-17 | 2016-03-02 | 广州派勒机械设备有限公司 | A kind of high-pressure nano homogenizer |
| KR101682007B1 (en) * | 2013-12-26 | 2016-12-02 | 주식회사 엘지화학 | Preparation method of graphene |
| CN105540575A (en) * | 2016-01-28 | 2016-05-04 | 成都新柯力化工科技有限公司 | Method for preparing graphene by using high-pressure homogenizer delamination |
-
2016
- 2016-05-06 CN CN201610295055.9A patent/CN105819438B/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20220289576A1 (en) * | 2019-07-09 | 2022-09-15 | Applied Graphene Materials Uk Limited | Dispersions |
Also Published As
| Publication number | Publication date |
|---|---|
| CN105819438A (en) | 2016-08-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105819438B (en) | A kind of method using aquashear prepare with scale nano-graphene material | |
| CN106542527B (en) | A kind of mechanical stripping grading system for graphene microchip dispersion liquid method | |
| CN104803380B (en) | Preparation method of graphene | |
| JP7190735B2 (en) | A low-cost and rapid method for mass production of graphene and graphene oxide using carbon-rich natural materials | |
| CN107108226B (en) | Method for preparing graphene by high-speed homogenization pretreatment and high-pressure homogenization | |
| CN106185895A (en) | A kind of graphene dispersion liquid and preparation method thereof | |
| CN104030272A (en) | Graphene peroxide preparation method | |
| CN101353477B (en) | Preparation of polyaniline / argentum nano composite material | |
| CN106185902B (en) | A kind of method that clean oxidation technology prepares the controllable graphene oxide of size | |
| EP3312142A1 (en) | A preparation method of graphene from graphene oxide based on mixed acid system | |
| CN103145121B (en) | Preparation method of thin-layer graphene oxide material | |
| CN105776193B (en) | A kind of method that graphene microchip is prepared using high voltage pulse water jet mill | |
| KR101573358B1 (en) | Nature-friendly graphene oxide manufaturing system using couette-taylor reactor | |
| CN106348263A (en) | Multilayer stable black phosphorene and preparation method | |
| CN110316707A (en) | A method of quickly preparing ion coordination modification black phosphorus nanometer sheet | |
| CN107381521A (en) | The preparation method of the graphite phase carbon nitride nanometer sheet of controlled oxygen functionalization | |
| CN104058393A (en) | Method for obtaining sheet layer two-dimensional material by stripping layered three-dimensional material | |
| CN105452161A (en) | Method for manufacturing graphite oxide and apparatus therefor | |
| CN105057690B (en) | A kind of preparation method of polymolecularity superfine spherical silver powder | |
| CN111003702B (en) | Two-dimensional laminar flow matrix carbon material composed of graphene nanosheets and preparation method thereof | |
| CN107055518B (en) | A kind of method for preparing graphene powder by pulverizing and the application of graphene powder | |
| Liu et al. | Alternating current assisted preparation of three-dimensional graphene aerogels and the application in electromagnetic interference shielding | |
| KR102097133B1 (en) | Method for preparation of highly concentrated graphene dispersion | |
| CN102528070B (en) | Method for producing nano-silver powder by means of high-speed jetting and device | |
| CN106587045A (en) | Production process of graphene oxide |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |