CN106154022B - A kind of application breathing graphene film in detection voltage stability - Google Patents
A kind of application breathing graphene film in detection voltage stability Download PDFInfo
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 155
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 104
- 238000001514 detection method Methods 0.000 title claims abstract description 9
- 230000029058 respiratory gaseous exchange Effects 0.000 title description 4
- 229910002804 graphite Inorganic materials 0.000 claims description 53
- 239000010439 graphite Substances 0.000 claims description 53
- 239000000243 solution Substances 0.000 claims description 26
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000012634 fragment Substances 0.000 claims description 14
- 239000012286 potassium permanganate Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 238000001914 filtration Methods 0.000 claims description 10
- 239000011261 inert gas Substances 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- 238000010792 warming Methods 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 229910001069 Ti alloy Inorganic materials 0.000 claims description 8
- 239000005457 ice water Substances 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 6
- 239000004575 stone Substances 0.000 claims description 6
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- 239000012752 auxiliary agent Substances 0.000 claims description 5
- 238000009826 distribution Methods 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- -1 Graphite alkene Chemical class 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000003638 chemical reducing agent Substances 0.000 claims description 4
- 229920002521 macromolecule Polymers 0.000 claims description 4
- 239000012528 membrane Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 230000009514 concussion Effects 0.000 claims description 3
- 230000007547 defect Effects 0.000 claims description 3
- 238000010790 dilution Methods 0.000 claims description 3
- 239000012895 dilution Substances 0.000 claims description 3
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 2
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims description 2
- 229920001661 Chitosan Polymers 0.000 claims description 2
- 108010010803 Gelatin Proteins 0.000 claims description 2
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims description 2
- 239000001099 ammonium carbonate Substances 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000008273 gelatin Substances 0.000 claims description 2
- 229920000159 gelatin Polymers 0.000 claims description 2
- 235000019322 gelatine Nutrition 0.000 claims description 2
- 235000011852 gelatine desserts Nutrition 0.000 claims description 2
- 229940113115 polyethylene glycol 200 Drugs 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 238000009288 screen filtration Methods 0.000 claims description 2
- 239000004156 Azodicarbonamide Substances 0.000 claims 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 claims 1
- 235000019399 azodicarbonamide Nutrition 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 235000013618 yogurt Nutrition 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 abstract description 13
- 230000035945 sensitivity Effects 0.000 abstract description 2
- 239000010408 film Substances 0.000 description 55
- 239000000463 material Substances 0.000 description 12
- 239000013078 crystal Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 150000001336 alkenes Chemical class 0.000 description 7
- 125000000524 functional group Chemical group 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- 238000002791 soaking Methods 0.000 description 4
- 238000007865 diluting Methods 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 241000446313 Lamella Species 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005485 electric heating Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000003019 stabilising effect Effects 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920006266 Vinyl film Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013039 cover film Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002305 electric material Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- 239000010742 number 1 fuel oil Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
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Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R19/00—Arrangements for measuring currents or voltages or for indicating presence or sign thereof
- G01R19/165—Indicating that current or voltage is either above or below a predetermined value or within or outside a predetermined range of values
- G01R19/16504—Indicating that current or voltage is either above or below a predetermined value or within or outside a predetermined range of values characterised by the components employed
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2204/00—Structure or properties of graphene
- C01B2204/20—Graphene characterized by its properties
- C01B2204/32—Size or surface area
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
The invention discloses one kind can breathe application of the graphene film in detection voltage stability, the application can breathe the electromagnetic shielding performance of graphene film by detection to realize, the electromagnetic shielding performance data that graphene film can be breathed are more unstable, and voltage stability is lower.The graphene film that breathes with heating conduction is rapidly heated expansion under external voltage, and shield effectiveness improves, the voltage value sensitivity with higher to power supply output.
Description
Technical field
The present invention relates to novel heat-conducting, the application of suction wave and electromagnetic shielding material more particularly to one kind can breathe graphite
Application of the alkene film in detection voltage stability.
Background technique
2010, two professor Andre GeiM and Konstantin Novoselov of Univ Manchester UK because
It is successfully separated out stable graphene for the first time and obtains Nobel Prize in physics, has started the upsurge that graphene is studied in the whole world.
Graphene has excellent electric property, and (electron mobility is up to 2 × 10 at room temperature5cM2/ Vs), heating conduction (5000W/ outstanding
(MK), extraordinary specific surface area (2630M2/ g), Young's modulus (1100GPa) and breaking strength (125GPa).Graphene is excellent
Different electrical and thermal conductivity performance is well beyond metal, while graphene has the advantages that corrosion-and high-temp-resistant, and its good machinery
Performance and lower density more allow it to have the potentiality in thermo electric material field substituted metal.
The graphene film of macroscopic view assembling graphene oxide or graphene nanometer sheet is the main application of nanoscale graphite alkene
Form.By further high-temperature process, the defect of graphene can be repaired, can effectively improve the electric conductivity of graphene film
And thermal conductance, it can be widely applied to smart phone, the intelligence high radiating requirements such as hardware, tablet computer, laptop with oneself
In accompanied electronic equipment.
The application of graphene film at present is limited to independent functional material, such as heat conducting film, conductive film, suction wave film, screen
Cover film.Single function is not obviously able to satisfy the demand of future technology progress complexity.For this purpose, we are using super large piece without fragment stone
Black alkene, which does substrate and devises, can breathe graphene film, one exhale complete thermal conductivity between a suction and inhale wave screen cover between function turn
It changes.The new thinking provided for the design of multifunction device.
Summary of the invention
The purpose of the present invention is overcome the deficiencies of the prior art and provide one kind to breathe graphene film in detection voltage stabilization
Application in property.
The purpose of the present invention is what is be achieved through the following technical solutions: the application can breathe graphene film by detection
Electromagnetic shielding performance realizes that the electromagnetic shielding performance data that can breathe graphene film are more unstable, voltage stability is lower.Institute
Graphene film of the average-size greater than 100 μm that graphene film can be breathed by planar orientation by stating passes through the pi-conjugated effect of π mutually overlap joint
It forms.The wherein graphene-structured comprising being made of 1-4 layers of graphene film.And the defect of graphene film is few, ID/TG<
0.01。
Further, it is described breathe graphene film the preparation method is as follows:
(1) it is 6~30mg/mL graphene oxide water that the graphene oxide by average-size greater than 100 μm, which is configured to concentration,
The auxiliary agent (i.e. the mass fraction of auxiliary agent in the solution is 0.1-5%) of mass fraction 0.1-5%, institute is added in solution in the solution
Stating auxiliary agent is inorganic salts, small organic molecule or macromolecule；After ultrasonic disperse, it is poured on Die and mould plate and is dried into graphene oxide membrane,
Then it is restored with reducing agent；
(2) graphene film after reduction is first warming up under atmosphere of inert gases with the rate of 0.1-0.5 DEG C/min
500-700 DEG C, keep the temperature 0.5-2h；
(3) it is warming up to 1000-1200 DEG C with the rate of 1-3 DEG C/min under atmosphere of inert gases, keeps the temperature 0.5-3h；
(4) it is warming up to 2500-3000 DEG C with the rate of 5-8 DEG C/min under atmosphere of inert gases, keeps the temperature 0.5-4h, it is natural
It can be obtained after cooling and porous breathe graphene film.
Further, the inorganic salts are selected from ammonium hydrogen carbonate；Small organic molecule is selected from urea, thiocarbamide, two formyl of azo
Amine, glycerol；Macromolecule is selected from cellulose, gelatin, chitosan, aqueous polyurethane, acrylic emulsion, polyethylene glycol 200, poly- second two
Alcohol 400.
Further, graphene oxide of the average-size greater than 100um obtains by the following method in the step 1:
(1) oxidized graphite flake for obtaining Modified-Hummer method reaction solution dilution after, in 140 mesh mesh screen into
Row filtering, obtains filtration product；
(2) filtration product for obtaining step 1 in ice water according to volume ratio 1:10 after mixing, stand 2h, dropwise plus
Enter hydrogen peroxide (H2O2Mass fraction be 30%), until the color of mixed liquor no longer changes, (potassium permanganate i.e. in mixed liquor is
It completely removes)；
(3) concentrated hydrochloric acid (concentration 12mol/L) is added dropwise into step 2 treated mixed liquor, until cotton-shaped oxygen
Graphite disappears, then goes out graphite oxide chip with the screen filtration of 140 mesh；
(4) the graphite oxide chip that step 3 obtains is placed in shaking table, 20~80 turns/min, concussion washing, so that oxidation
Graphite wafer removing obtains the graphene oxide of no fragment super large piece, and average-size is greater than 100um, and breadth coefficient is in 0.2-0.5
Between.
Further, the Modified-Hummer method in the step 1 specifically: at -10 DEG C, potassium permanganate is filled
Point be dissolved in the concentrated sulfuric acid that mass fraction is 98%, graphite be added, stops stirring after 60 revs/min of stirring 2h, low temperature (-
10-20 DEG C) under react 6-48h, obtain the oxidized graphite flake reaction solution of wide distribution；Graphite, potassium permanganate and the concentrated sulfuric acid
Mass volume ratio are as follows: the granularity of 1g:2-4g:30-40ml, graphite are greater than 150 μm.
Further, the mesh screen is the acidproof mesh screens such as titanium alloy.
Further, in the step 1, the reaction solution of oxidized graphite flake is diluted by diluents such as the concentrated sulfuric acids, dilute
The volume for releasing agent is 1-10 times of reaction solution volume.
Disclosure sets forth a kind of multifunctional graphite vinyl films that can be converted between heating conduction and electromagnetic shielding performance
New opplication, and the graphene film is mutual by the pi-conjugated effect of π greater than 100 μm of graphene film by the average-size of planar orientation
It is formed by overlapping.Big conjugated structure ensure that the unimpeded of the access between graphene, and the graphene knot that 1-4 layers of graphene film is constituted
The introducing of structure is greatly improved the electric conductivity of material；In non-lap-joint, cavity is formed between graphene film and piece；By stone
Black alkene film is connected with outer load power supply, the quick conductive under the electric heating property of graphene, the expansion so that its intracavity gas is rapidly heated,
On the other hand, under high temperature, fold itself has the tendency that unfolding, meanwhile, under gas expansion effect, the fold of cavity wall is supportted by gas
It opens, gradually becomes smooth；Big cavity, smooth cavity wall auxiliary make its film have extremely strong electromagnetic shielding with preferable electric conductivity
Performance.Voltage is higher, and electromagnetic shielding performance is better.When needing to reuse, micro- air bag is compressed using condition of high voltage
?.
Detailed description of the invention
Fig. 1 is the graphite oxide crystal (left side) before filtering, filtered graphite oxide crystal (right side).
Fig. 2 is the graphene oxide (left side) before filtering, filtered graphene oxide (right side).
Fig. 3 is 50 degree and reacts obtained graphene oxide down.
Fig. 4 is 50 degree and reacts obtained graphene oxide size distribution (left side) down, and 20 degree are reacted obtained graphite oxide down
Alkene size is distributed (right side).
Fig. 5 is that can breathe graphene film to exhale and inhale state lower section figure.
Fig. 6 is the electromagnetic shielding curve graph under voltage loads.
Specific embodiment
By the present invention in that being formed a film with super large piece graphene oxide, wherein the average-size of planar orientation is greater than 100 μm
Graphene film important role, present invention during constituting graphene film of the present invention wash it in graphite oxide crystal
Before, the method separated using mesh screen is isolated fragment.And use 10 times to be diluted with the ice water of upper volume, so that it is brilliant
Piece will not be destroyed because of the heat of solution of sulfuric acid.Further using shaking table concussion washing, so that graphene oxide layer is being shelled
From when avoid the broken of mechanical force.Further, the present invention also passes through cryogenic conditions and prepares graphene film, in low temperature
Under, potassium permanganate oxidation is weaker, and the rate that selfdecomposition generates oxygen is slow, therefore gas is to graphite oxide crystal
Fragmentation is just very weak, so that the graphene oxide of big lamella is saved.And do not have in reaction process and cleaning process
Violent stirring and ultrasonic procedure, thus lamella there is no it is broken.In summary some, we have obtained the nothing of super large piece
The graphene oxide of fragment, average-size are greater than 87um, and for breadth coefficient between 0.2-0.5, shive content is lower than 1%.
The invention will be further described with reference to the accompanying drawings and embodiments.The present embodiment be served only for being the present invention into
The explanation of one step should not be understood as limiting the scope of the invention, and those skilled in the art is according in foregoing invention
Appearance makes some nonessential changes and adjustment, all belongs to the scope of protection of the present invention.
Embodiment 1: the preparation of the graphene oxide without fragment super large piece
Embodiment 1-1
(1) potassium permanganate is slowly added into the concentrated sulfuric acid quickly stirred at -10 DEG C, to after completely dissolution, be added
Graphite, 60 revs/min are slowly stirred stopping stirring after 2h, react 6h respectively at 20 DEG C, 50 DEG C, respectively obtain the oxygen of wide distribution
Graphite crystal；As shown in Figure 1, there is more fragment in the graphite oxide chip obtained at a temperature of two kinds, this makes it
Corresponding graphene oxide equally has many fragments (Fig. 2).
(2) (extension rate can be any multiple to the reaction solution diluting concentrated sulfuric acid obtained step 1, and the present embodiment is dilute
Release 10 times or so), and graphite oxide crystal is filtered out into (reaction solution time with the titanium alloy mesh screen of the aperture 150um (140 mesh)
Receive), and be poured slowly into the ice water relative to 10 times of volumes of filtration product quickly stirred, 2h is stood, H is slowly added to2O2, with
Except potassium permanganate extra in dereaction, suitable hydrochloric acid is added until cotton-shaped graphite oxide disappears, then with titanium alloy mesh screen
(140 mesh) filters out graphite oxide chip；Shaking table slowly shakes washing, and the graphene oxide for obtaining no fragment super large piece is (average
Having a size of 87um, breadth coefficient 0.5).Graphite, potassium permanganate and concentrated sulfuric acid mass volume ratio are as follows: 1g:2g:40ml, graphite
Granularity is 200um.
As shown in figure 3, the oxidation stone washed after the graphite oxide chip separation isolated after 50 degree of high temperature lower reactions
Black alkene equally has many fragments；From fig. 4, it can be seen that large stretch of graphene oxide size under low temperature after (20 DEG C) Reaction Separation
It is distributed more uniform concentration, shive content is few.
Embodiment 1-2
Potassium permanganate is slowly added into the concentrated sulfuric acid quickly stirred at -10 DEG C, to after completely dissolution, stone be added
Ink, 60 revs/min are slowly stirred stopping stirring after 2h, react 48h under low temperature (0 DEG C), obtain reaction solution；By reaction solution point
It is not diluted with the concentrated sulfuric acid of 98% or more mass fraction, the dilute sulfuric acid that mass fraction is 10%, then with the aperture 150um
Graphite oxide crystal is filtered out (reaction solution recycling) by titanium alloy mesh screen, and be poured slowly into quickly stir relative to filtering produce
In the ice water of 10 times of volumes of object, 2h is stood, H is slowly added to2O2, suitable salt is added except potassium permanganate extra in dereaction
Acid disappears until cotton-shaped graphite oxide, then is sieved through with titanium alloy reticulated and filters out graphite oxide chip；Shaking table slowly shakes washing, obtains
Reaction product.Graphite, potassium permanganate and concentrated sulfuric acid mass volume ratio are as follows: 1:4g:30ml；The granularity of graphite is 500um.
Using diluting concentrated sulfuric acid, (average-size 98um is distributed the graphene oxide without fragment super large piece reacted
Coefficient is diluted with dilute sulfuric acid 0.4), a large amount of fragments is contained in obtained product, size breadth coefficient is more than 100%.This is
It is highly exothermic due in dilute sulfuric acid dilution, destroy graphite oxide crystal.
Embodiment 1-3
Potassium permanganate is slowly added into the concentrated sulfuric acid quickly stirred at -10 DEG C, to after completely dissolution, stone be added
Ink, 60 revs/min are slowly stirred stopping stirring after 2h, react 28h under low temperature (20 DEG C), the graphite oxide for obtaining wide distribution is brilliant
Body；Graphite oxide crystal is filtered out into (reaction solution by reaction solution diluting concentrated sulfuric acid and with the titanium alloy mesh screen in the aperture 150um
Recycling), and be poured slowly into respectively quickly stir relative to 5 times of volumes of filtration product, 8 times of volumes, 10 times of volumes ice water in,
2h is stood, H is slowly added to2O2, suitable hydrochloric acid is added until cotton-shaped graphite oxide except potassium permanganate extra in dereaction
It disappears, then is sieved through with titanium alloy reticulated and filters out graphite oxide chip；Shaking table slowly shakes washing, obtains reaction product；Graphite, Gao Meng
Sour potassium and concentrated sulfuric acid mass volume ratio are as follows: 1:5g:34ml, the granularity of graphite are 2mm.
Experimental result shows, the ice water of 5 times of volumes and 8 times of volumes cannot obtain the graphene film of size uniformity,
The graphene oxide of no fragment super large piece can be just obtained under 10 times of volumes, and (average-size 92um, breadth coefficient is 0.2).Thus
It is found that the amount of ice water is too low, it will be so that the heat of mixing concentrates release, destruction crystal structure.
Embodiment 2: respirable graphite is prepared using the graphene oxide without fragment super large piece that embodiment 1 is prepared
Alkene film.
It is 30mg/mL graphene oxide water solution that graphene oxide by average-size greater than 100um, which is configured to concentration,
5% urea of mass fraction is added in solution, is poured on Die and mould plate after ultrasonic disperse and is dried into graphene oxide membrane, then used
Hydrogen iodide reducing agent is restored；Graphene film after reduction under atmosphere of inert gases according to heat shown in 1~table of table 3 at
Reason mode carries out three step heat treatments；The porous graphene film with a thickness of 1mm can be obtained after Temperature fall.By graphene film
Compacting can obtain super flexible high thermal conductivity graphene film under high pressure.The pressing process pressure is 200MP, time 300h.
Above-mentioned resulting graphene film is suppressed into 2h under the high pressure of 50MP；Measure its thermal conductivity；By pressed graphite
Alkene film loads 20V external voltage, so that it is rapidly heated with 200 DEG C/min to 600 DEG C, after natural cooling, measures its electromagnetic shielding
Performance prepares the parameter of high thermal conductivity and highly sensitive graphene film with acquisition；As shown in table 1-3.Fig. 5 is that can breathe graphite
Alkene film respiratory electromicroscopic photograph, during exhaling under external force, graphene film is driven plain, and breathing stomata passes through fold
Form remain；During suction under electroluminescent heat effect, fold is strutted by gas, gradually becomes smooth.
Table 1: the heat treatment mode of the first step
Table 2: the heat treatment mode of second step
Table 3: the heat treatment mode of third step
From 1~table of table 3 as can be seen that being determined in terms of the performance of this material mainly has three, one material internal graphite oxide
Alkene chip architecture repair situation, i.e., functional group fall off and high temperature under carbon conjugated structure reparation.Second, material internal three-dimensional takes
To the continuity of structure, i.e., the connectivity of internal lamellar structure.Third, the formation of micro- air bag just can guarantee material flexibility and
The presence of graphene sheet layer structure.Three's collective effect is to increase the performance of graphene film.
As it can be seen from table 1 comparing A1, B1, C1, D1, E1, the temperature of A1 is too low, is not enough to remove most of degradable
Functional group, cause gas in second step pyroprocess largely quickly to generate, tear lamellar structure at high temperature；E1 temperature mistake
Height, generation gas is too fast, can largely tear material internal structure, both can make deterioration in material properties.Have only B1, C1,
At a temperature of D1, functional group will be slow and thoroughly remove, to ensure material property.Compare C1, F1, G1, H1, F1 heating rate mistake
Low, gas release is excessively slow, and material internal cannot be made to form through-hole, be unfavorable for micro- air bag in next temperature-rise period
Formation；H1 temperature-rise period is too fast, and gas release is too fast, tears material internal structure, is unfavorable for forming transmission channel.Have CG only
It just can not only guarantee the formation of micro- air bag under heating rate, but also can guarantee the complete of channel.Compare C1, I1, J1, K1, L1, M1,
I1 soaking time is too short, it cannot be guaranteed that the degradation of most of functional group；M1 insulating process is too long, can absorb the coke inside stove
Oil is unfavorable for the promotion of performance.C1, J1, K1, L1 just avoid both of the above.
From Table 2, it can be seen that comparing A2, B2, C2, D2, E2, A2 heating rate is too low to be not enough to be formed small gap
Structure, prevent film seriously affects electromagnetic shielding performance from forming micro- air bag.E2 heating rate is excessively high, can tear graphene layer
Between structure so that graphene film link property is deteriorated, thermally conductive electromagnetic shielding performance is all deteriorated.Have the heating rate of B2, C2, D2 only
Under, it just capable can not only guarantee micro- airbag structure but also guarantee the continuity inside graphene film.Compare C2, I2, J2, K2, L2,
M2, I2 soaking time are too short, and stable functional group cannot sufficiently fall off；M2 overlong time, graphene film are easy tar adsorption, no
Conducive to the promotion of film properties；And sufficiently falling off for stabilising functional group can be not only guaranteed under the conditions of C2, J2, K2, M2, but also be avoided that coke
The puzzlement of oil.
From table 3 it is observed that comparing A3, B3, C3, D3, E, A3 heating rate is too low, the mistake that most stabilising functional group falls off
Slowly, it is not enough to support the formation of micro- air bag during forming micro- air bag；E3 temperature-rise period is too fast, and gas release and high temperature are swollen
It is swollen too fast, it is easily destroyed the formation of micro- air bag.Only in the case where B3, C3, D3, the formation that micro- air bag could be stable, graphene
On structure could slowly repair.Compare C3, F3, G3, H3, I3, F3 outlet temperature is too low, and graphene-structured is repaired not complete enough
It is kind, so various performances are all very poor；I3 outlet temperature is excessively high, and graphene can be vaporized；It could both at a temperature of C3, G3, H3
Guarantee the reparation of graphene-structured, and will not be vaporized.Compare C3, J3, K3, L3, M3, J3 soaking time is too low, graphene
Structure cannot be repaired sufficiently, and M3 soaking time is too long, can also to adsorb the tar in furnace body, be influenced the performance of film.
Embodiment 3: graphene film is used to detect voltage swing.
Firstly, can to breathe graphene film as follows for preparation
(1) it is 6mg/mL graphene oxide water solution that the graphene oxide by average-size greater than 100 μm, which is configured to concentration,
The glycerol of mass fraction 5% is added in the solution；It after ultrasonic disperse, is poured on Die and mould plate and is dried into graphene oxide membrane, then
It is restored with reducing agent；
(2) graphene film after reduction is first warming up to 700 under atmosphere of inert gases with the rate of 0.5 DEG C/min
DEG C, keep the temperature 1h；
(3) 1200 DEG C are warming up to the rate of 2 DEG C/min under atmosphere of inert gases, keep the temperature 1h；
(4) 2500 DEG C are warming up to the rate of 7 DEG C/min under atmosphere of inert gases, keep the temperature 1h, after Temperature fall
It obtains porous breathing graphene film.
Then, the graphene film being prepared is connected with multiple constant voltage source I~VIII respectively, constant voltage source I~
The voltage value of VIIII is as shown in the table.
| I | II | III | IV | V | VI | VII | VIII |
| 1V | 3V | 6V | 8V | 11V | 15V | 18V | 20V |
Energization 10min, the electromagnetic shielding data measured are as shown in Figure 6.
As can be seen from Figure 6, graphene film has the electric heating property and thermal conductivity of superelevation, substantially completes to lead in 0.5 minute
Thermal technology makees, high sensitivity.In addition, the graphene film electromagnetic shielding performance size discrimination under different voltages is obvious, explanation can identify
Different voltages size, voltage is bigger, and electromagnetic shielding performance is bigger.Therefore, efficient evaluations can be carried out to voltage stability.
Claims (7)
1. one kind can breathe application of the graphene film in detection voltage stability, which is characterized in that the application passes through detection
The electromagnetic shielding performance of graphene film can be breathed to realize, the electromagnetic shielding performance data that can breathe graphene film are more unstable,
Voltage stability is lower；The graphene film that graphene film is breathed by the average-size of planar orientation greater than 100 μm passes through π
Pi-conjugated effect is mutually formed by overlapping；In non-lap-joint, cavity is formed between graphene film and piece, has fold in cavity wall, can be breathed
Graphene-structured in graphene film comprising being made of 1-4 layers of graphene film；And the defect of graphene film is few, ID/IG<
0.01。
2. application according to claim 1, which is characterized in that it is described breathe graphene film the preparation method is as follows:
(1) it is 6 ~ 30mg/mL graphene oxide water solution that the graphene oxide by average-size greater than 100 μm, which is configured to concentration,
The auxiliary agent of mass fraction 0.1-5% is added in the solution, the auxiliary agent is inorganic salts, small organic molecule or macromolecule；Ultrasonic disperse
Afterwards, it is poured on Die and mould plate and is dried into graphene oxide membrane, then restored with reducing agent；
(2) by the graphene film after reduction under atmosphere of inert gases first with 0.1-0.5oThe rate of C/min is warming up to 500-
700oC keeps the temperature 0.5-2h；
(3) with 1-3 under atmosphere of inert gasesoThe rate of C/min is warming up to 1000-1200oC keeps the temperature 0.5-3h；
(4) with 5-8 under atmosphere of inert gasesoThe rate of C/min is warming up to 2500-3000oC keeps the temperature 0.5-4h, Temperature fall
After can be obtained and porous breathe graphene film.
3. application according to claim 2, which is characterized in that the inorganic salts are selected from ammonium hydrogen carbonate；Small organic molecule
Selected from urea, thiocarbamide, azodicarbonamide, glycerol；Macromolecule is selected from cellulose, gelatin, chitosan, aqueous polyurethane, propylene
Yogurt liquid, polyethylene glycol 200, polyethylene glycol 400.
4. application according to claim 3, it is characterised in that, average-size is greater than the oxygen of 100 um in the step (1)
Graphite alkene obtains by the following method:
(1) it after the reaction solution dilution for the oxidized graphite flake for obtaining Modified-Hummer method, was carried out in the mesh screen of 140 mesh
Filter, obtains filtration product；
(2) filtration product for obtaining step 1 in ice water according to volume ratio 1:10 after mixing, stand 2h, matter is added dropwise
The hydrogen peroxide that score is 30% is measured, until the color of mixed liquor no longer changes；
(3) concentrated hydrochloric acid that concentration is 12mol/L is added dropwise into step 2 treated mixed liquor, until cotton-shaped oxidation stone
Ink disappears, then goes out graphite oxide chip with the screen filtration of 140 mesh；
(4) the graphite oxide chip that step 3 obtains is placed in shaking table, 20 ~ 80 turns/min, concussion washing, so that graphite oxide
Chip removing, obtains the graphene oxide of no fragment super large piece, and average-size is greater than 100 um, breadth coefficient 0.2-0.5 it
Between.
5. application according to claim 4, which is characterized in that the Modified-Hummer method in the step 1 is specific
Are as follows: -10oUnder C, potassium permanganate is completely dissolved in the concentrated sulfuric acid that mass fraction is 98%, graphite is added, 60 revs/min are stirred
Stop stirring after mixing 2h, in -10-20o6-48h is reacted in a low temperature of C, obtains the oxidized graphite flake reaction solution of wide distribution；It is described
Graphite, potassium permanganate and concentrated sulfuric acid mass volume ratio are as follows: 1 g:2-4g:30-40ml, the granularity of graphite are greater than 150 μm.
6. application according to claim 4, which is characterized in that the mesh screen is the acidproof mesh screen of titanium alloy.
7. application according to claim 4, which is characterized in that in the step 1, the reaction solution of oxidized graphite flake passes through dilute
It releases the agent concentrated sulfuric acid to be diluted, the volume of diluent is 1-10 times of reaction solution volume.
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