CN114014305A - Preparation method of graphene heat-conducting film - Google Patents
Preparation method of graphene heat-conducting film Download PDFInfo
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- CN114014305A CN114014305A CN202111523307.6A CN202111523307A CN114014305A CN 114014305 A CN114014305 A CN 114014305A CN 202111523307 A CN202111523307 A CN 202111523307A CN 114014305 A CN114014305 A CN 114014305A
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 198
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 178
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 36
- 238000005056 compaction Methods 0.000 claims abstract description 11
- 238000010304 firing Methods 0.000 claims abstract description 5
- 229910002804 graphite Inorganic materials 0.000 claims description 20
- 239000010439 graphite Substances 0.000 claims description 20
- 238000010438 heat treatment Methods 0.000 claims description 12
- 239000002510 pyrogen Substances 0.000 claims description 9
- 238000003825 pressing Methods 0.000 claims description 5
- 238000005096 rolling process Methods 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
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- 238000007669 thermal treatment Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- F28D15/02—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies in which the medium condenses and evaporates, e.g. heat pipes
- F28D15/04—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies in which the medium condenses and evaporates, e.g. heat pipes with tubes having a capillary structure
- F28D15/046—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies in which the medium condenses and evaporates, e.g. heat pipes with tubes having a capillary structure characterised by the material or the construction of the capillary structure
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Abstract
The invention provides a preparation method of a graphene heat-conducting film, which comprises the following steps: reducing the graphene oxide film by adopting a flame firing method; carrying out first compaction treatment on the graphene oxide subjected to flame reduction treatment; then carrying out high-temperature thermal reduction; and performing a second compaction process. The invention adopts flame to quickly reduce, so that a plurality of capillary gas channels are formed in the film body, and thus, the generated gas can be discharged along the formed capillary gas channels during the subsequent reduction, the gas is prevented from being accumulated in the film body, and the increase of the film thickness can be effectively reduced.
Description
The application is a divisional application, and the application number of a parent case is as follows: 202010257865.1, the filing date of the parent: the invention name of the mother case is as follows, 04/03/2020: a method of flame reducing a graphene oxide film and a graphene film.
Technical Field
The invention relates to the field of preparation of graphene films, in particular to a method for reducing graphene oxide.
Background
Heretofore, in the preparation technology of graphene heat-conducting films, graphene oxide is directionally assembled and prepared into a graphene oxide film, and the graphene oxide heat-conducting film in directional arrangement is finally obtained through thermal reduction, so that the graphene heat-conducting film has a very high heat conductivity coefficient which is not less than 1000W/m.K, and is widely applied to electronic products such as mobile phones, computers and the like.
However, since a large amount of gas is discharged from the oxygen-containing functional group in the graphene oxide during thermal reduction to form a capillary gas channel, the graphene oxide film expands very thickly during the thermal reduction process, and the expanded thickness is 2.2-3 times of the original thickness of the graphene oxide film, so that the capacity of thermal treatment equipment is reduced, and the energy consumption of thermal treatment is high. Therefore, solving or reducing the thickness expansion of the graphene oxide film in the thermal reduction process is an urgent work with great significance.
The statements in the background section are merely prior art as they are known to the inventors and do not, of course, represent prior art in the field.
Disclosure of Invention
In view of one or more of the problems in the prior art, the present invention provides a method for reducing a graphene oxide film, in which the graphene oxide film is reduced by a flame firing method.
According to one aspect of the invention, the method for flame firing heating is specifically as follows: the graphene oxide film is passed over the flame where it contacts the outer flame of the flame.
According to one aspect of the invention, the temperature at the outer flame of the flame is 300-. In general, a combustion flame of natural gas is used to form capillary gas channels in a graphite oxide film body in a graphene oxide film.
Preferably, the flame has a temperature at the outer flame of 400 ± 50 ℃.
According to one aspect of the invention, the speed of the passing is 0.5-5 m/min. The film is heated all the time when the speed is too low, and the heat is transferred to the unfired place in a conduction mode, so that the unfired place is deformed, and the appearance of the film is inconsistent and uneven; the passing speed is too fast, which easily causes incomplete burning. Long-term tests show that when the passing speed is controlled to be 0.5-5 m/min, the uniformity of flame treatment can be effectively ensured, the flatness of the outer surface of the film is consistent, and the formed capillary gas channels are high in size consistency and uniform in distribution. The passing speed is 1-2m/min, the effect is better.
The invention also provides a preparation method of the graphene film, which comprises the following steps:
carrying out flame reduction treatment on the graphene oxide film by adopting the method;
then carrying out high-temperature pyrogen reduction; and
and compacting to obtain the graphene film.
According to one aspect of the invention, the high temperature pyrogen reduction temperature is 2000-3000 ℃.
According to one aspect of the invention, the specific method of high-temperature pyrogen reduction is as follows: and (3) placing the reduced graphene oxide film in thermal reduction equipment, gradually increasing the temperature in the equipment from room temperature to 2000-3000 ℃, wherein the temperature increasing speed is 2-10 ℃/min.
Preferably, the temperature in the pyrogen reduction equipment is increased from room temperature to 600 ℃ at the temperature rising speed of 2 ℃/min; further preferably, the temperature in the pyrogen reduction equipment is increased from 600 ℃ to the final reduction temperature at a temperature rise speed of 4-5 ℃/min. After the flame reduction treatment, the graphene oxide also contains a large amount of oxygen-containing functional groups, so that the film further expands due to the fact that the temperature rising speed is too high. Through repeated adjustment and research, the graphene oxide film subjected to fire trap reduction is subjected to the staged temperature rise during high-temperature treatment, so that the efficiency is high, and the yield is high.
According to one aspect of the invention, the reduced graphene oxide film is subjected to constant temperature treatment at 2000-3000 ℃ for 45-80 min.
Preferably, a plurality of graphene oxide films are stacked together to perform batch graphitization treatment; further preferably, each adjacent photo graphene oxide film is separated by graphite paper.
According to one aspect of the invention, the step of compacting adopts rolling or flat pressing, and the pressure is more than or equal to 20 MPa. The pressure is preferably 25 to 60 MPa.
According to one aspect of the invention, after the flame reduction treatment of the graphene oxide film and before the high-temperature thermal reduction treatment, the graphene oxide film subjected to flame reduction is compacted, and the graphene oxide film is rolled or pressed flatly under the pressure of more than or equal to 5 MPa. The pressure is preferably 10-15 MPa.
According to one aspect of the invention, the graphene oxide film is prepared by dispersing, coating, drying and stripping graphene oxide slurry, and preferably, the thickness of the graphene oxide film is 4-300 μm.
The invention adopts flame to quickly reduce, so that a plurality of capillary gas channels are formed in the film body, and thus, the generated gas can be discharged along the formed capillary gas channels during the subsequent reduction, the gas is prevented from being accumulated in the film body, and the increase of the film thickness can be effectively reduced.
Drawings
The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention and not to limit the invention. In the drawings:
FIG. 1 is a photograph showing the appearance of a graphene oxide film (raw material film) in the method of the present invention;
FIG. 2 is a photograph of the appearance of a sample of the graphene oxide monolayer film after the flame reduction treatment of example 1;
FIG. 3 is a photograph of the appearance of a sample of the graphene foam film of example 1 (after high temperature treatment and before densification);
FIG. 4 is an SEM image of a graphene thermal conductive film obtained by the method of example 1;
FIG. 5 is the appearance of the two graphene oxide layers after flame reduction treatment and densification of example 2;
fig. 6 is a photograph of the appearance of a sample of the graphene foam film of example 2 (after high temperature treatment and before densification);
fig. 7 is an SEM image of the graphene thermal conductive film of example 2;
fig. 8 is a photograph of the appearance of a sample of the graphene film of example 3;
FIG. 9 is an SEM image of a graphene film obtained by the method of example 3;
fig. 10 is the climbing phenomenon of the graphene film in water of example 3;
FIG. 11 is an appearance of a graphene film obtained by the method of comparative example 1;
fig. 12 is an SEM image of the graphene film obtained by the method of comparative example 1;
fig. 13 is an appearance of the graphene film obtained by the method of comparative example 2;
fig. 14 is an SEM image of the graphene film obtained by the method of comparative example 2.
Detailed Description
In the following, only certain exemplary embodiments are briefly described. As those skilled in the art will recognize, the described embodiments may be modified in various different ways, all without departing from the spirit or scope of the present invention. Accordingly, the drawings and description are to be regarded as illustrative in nature, and not as restrictive.
In one embodiment of the present invention, a novel method for reducing graphene oxide films, i.e., flame reduction, is presented. The method is described in detail below.
The graphene oxide film is selected from the graphene oxide films manufactured by the company in mass production, and the graphene oxide film is prepared by adopting a graphene oxide self-assembly oriented arrangement method which comprises the steps of dispersing, coating, drying, stripping and slitting. Or obtaining a strip-shaped graphene oxide film without slitting, wherein the thickness of the graphene oxide film is 40-300 mu m; see patent documents CN201510481379.7, CN201510480016.1 for specific methods.
And (2) reducing the graphene oxide film by adopting flame, wherein the flame is formed by burning natural gas, the temperature of the flame is 300-600 ℃, the graphene oxide film passes through the flame, and the speed of the graphene oxide film passing through the outer flame of the flame is 0.5-5 m/min. The film is heated all the time when the speed is too low, and the heat is transferred to the unfired place in a conduction mode, so that the unfired place is deformed, and the appearance of the film is inconsistent and uneven; the passing speed is too fast, which easily causes incomplete burning. Long-term tests show that when the passing speed is controlled to be 0.5-5 m/min, the uniformity of flame treatment can be effectively ensured, the flatness of the outer surface of the film is consistent, and the formed capillary gas channels are high in size consistency and uniform in distribution. In this embodiment, the flame is preferably passed through the outer flame at 1 to 2 m/min. The thickness of the graphene oxide film reduced by flame is 300-3000 mu m. The aim of flame reduction is to decompose functional groups of graphene oxide at a high temperature, and to expand graphene sheets to form capillary gas channels, so that gas generated in the thermal reduction process of the graphene oxide film is reduced, and a large amount of gas generated in the thermal reduction process can be effectively discharged out of the film body from the capillary gas channels, and finally expansion of the thickness of the graphene oxide film in the thermal reduction process is reduced. During the flame treatment, the gas is rapidly discharged, so that a plurality of capillary gas passages are formed, and the generated gas can be discharged from the capillary gas passages during the subsequent heat treatment. In many experiments, we have found that these capillary gas channels produced by fire trap reduction are very small (typically within 1 micron) and are not destroyed by physical compaction. The hydrogen bonding effect during the self-assembly of the graphene oxide film is compared to form tight combination between the sheets, and gas discharge in the reduction process is prevented, so that the integral thickness of the film is increased in the reduction process. The invention adopts the capillary gas channel generated by flame reduction, so that the gas can be rapidly discharged, the gas is prevented from being accumulated in the film body, and the increase of the film thickness can be effectively reduced.
In another embodiment of the present invention, a graphene oxide film prepared by directionally assembling graphene oxide is shown, and the graphene oxide film is obtained from a graphene oxide film normally produced by the company (see patent CN201510481379.7, CN201510480016.1), the graphene oxide film is reduced by using flame, and then is compacted to obtain a flame-reduced graphene oxide film, and then is further reduced at high temperature to obtain a reduced graphene foam film, and is further compacted to obtain a graphene thermal conductive film.
The specific preparation method comprises the following steps:
1. the graphene oxide film is selected from the graphene oxide films manufactured by the company in mass production, and the graphene oxide film is prepared by adopting a graphene oxide self-assembly oriented arrangement method which comprises the steps of dispersing, coating, drying, stripping and slitting. The thickness of the graphene oxide film is 40-300 mu m;
2. reducing the graphene oxide film by adopting the flame reduction method;
3. compacting the graphene oxide film reduced by the flame to obtain a compacted graphene oxide film reduced by the flame; the compaction can be realized by a double-roller machine or a flat press, and the compaction pressure is more than 5 MPa;
the single-layer flame-reduced graphene oxide film can be compacted by compaction, and the thickness is 50-400 mu m; or the multilayer flame-reduced graphene oxide films can be stacked together and compacted, and the thickness is more than 200 mu m and reaches millimeter level or centimeter level;
4. further carrying out thermal reduction on the compacted graphene oxide film reduced by the flame to obtain a reduced graphene foam film; graphene oxide films reduced by flame are stacked and placed in a graphite boat, the layers of the graphene oxide films are separated by graphite paper, the graphite paper is formed by pressing expanded graphite, the thickness of the graphite paper is 150-350 microns, the too thin graphite paper serving as an interlayer has insufficient stiffness, the edge of the finally obtained graphene heat-conducting film is poor, the too thick graphite paper occupies space, and the productivity is affected; the thermal reduction temperature of the graphene oxide film reduced by the flame is 2000-3000 ℃, the temperature is increased from room temperature to the highest temperature, and the temperature increasing speed is 2-10 ℃/min; the thickness of the obtained graphene foam film is 50-400 mu m in a single layer and more than 200 mu m in multiple layers, and the density of the graphene foam film is 0.4-1.1 g/cm3The density is more than 2 times of the density of the graphene foam film obtained by the existing thermal reduction process; the density of the graphene foam film is greatly improved, the thickness is reduced, and the graphene foam film is simpleThe furnace capacity is greatly improved, and the thermal reduction cost is effectively reduced; compared with the following specific example 1 and comparative example 1, the graphene oxide films used in the two specific examples are the same, the flame reduction treatment is not performed in the comparative example 1, the flame reduction treatment is performed in the example 1, and the yield is improved by 37.8% compared with the comparative example 1 because 1622 graphene films can be burnt in a single furnace in the comparative example 1 and 2235 graphene films can be burnt in a single furnace in the example 1 when the two specific examples are processed at high temperature.
5. And further compacting the obtained graphene foam film to obtain the graphene film, wherein the compacting can be performed by rolling or flat pressing, the pressure is not less than 20MPa, and in the embodiment, the pressure is controlled within the range of 25-60 MPa. The thickness of the compacted graphene film is micron-sized, is more than 10 micrometers, generally is 30-400 micrometers, the heat conductivity coefficient is more than or equal to 1000W/m.K, and the density is more than or equal to 1.9g/cm3。
Another embodiment of the present invention shows another method for preparing a graphene film, in which the graphene film obtained by the method is lighter than the graphene film obtained by the previous embodiment, and can be used as a lighter electromagnetic shielding material, a heat conducting support of a heat storage material, a capillary wick of a heat pipe, and the like. According to the method, the graphene oxide film reduced by flame is directly subjected to further thermal reduction without compaction, so that the graphene oxide film with lower density can be obtained, and the density can reach 0.02-0.07 g/cm 3. In the embodiment, the treatment temperature of the further thermal reduction is 800-3000 ℃, and the rate of rising from room temperature to the maximum temperature is 2-10 ℃/min; nitrogen or argon is used as the protective gas.
The preferred embodiments of the present invention will be described in conjunction with the accompanying drawings, and it will be understood that they are described herein for the purpose of illustration and explanation and not limitation.
Example 1:
a preparation method of a graphene film as a heat conducting film comprises the following steps:
as shown in FIG. 1, a graphene oxide film produced and manufactured by this company and oriented self-assembly was used as a raw material film, and had a thickness of 138 μm.
And (3) reducing the graphene oxide film by flame at 500 ℃ to obtain the flame-reduced graphene oxide film, wherein the thickness of the flame-reduced graphene oxide film is 1216 mu m. The appearance of the graphene oxide film after flame reduction is shown in fig. 2.
And rolling and compacting the flame reduced graphene oxide film by a roll squeezer, wherein the pressure of the roll squeezer is 10MPa, and the thickness of the compacted flame reduced graphene oxide film is 188 micrometers. The above-mentioned compacted flame-reduced graphene oxide films were stacked in layers, separated by 150 μm graphite paper, stacked in a graphite boat, and subjected to thermal reduction. The temperature in the graphite boat is increased from room temperature to 2850 ℃, wherein the temperature is increased from the room temperature to 600 ℃ by adopting 2 ℃/min, the temperature is increased from 600 ℃ to 2850 ℃ by adopting 4 ℃/min, the temperature is increased to 2850 ℃ and then is kept for 1h, the thickness of the obtained reduced graphene foam film is 184 mu m, and the density is 0.43g/cm3As shown in fig. 3. Compacting the graphene foam film by adopting a roller press under the pressure of 25MPa to obtain the graphene foam film with the thickness of 38 mu m and the density of 2.06g/cm3The thermal conductivity coefficient of the graphene thermal conductive film is 1560W/m.K. An SEM image of the obtained graphene thermal conductive film is shown in fig. 4.
Example 2:
a preparation method of a graphene film as a heat conducting film comprises the following steps:
in the first example, two graphene oxide films obtained by flame reduction were stacked together and compacted by a flat press, the pressure of the flat press was 15MPa, and the thickness of the two graphene oxide films obtained by flame reduction and compacted by stacking was 360 μm (as shown in fig. 5). The above-described compacted flame-reduced graphene oxide films were stacked in layers separated by graphite paper of 300 μm, stacked in a graphite boat, and subjected to thermal reduction. The temperature in the graphite boat is raised from room temperature to 2900 ℃, the temperature is maintained for 1h, the temperature is raised from room temperature to 600 ℃ by adopting 2 ℃/min, the temperature is raised from 600 ℃ to 2900 ℃ by adopting 5 ℃/min, the thickness of the obtained reduced graphene foam film is 276 mu m, and the density is 0.56g/cm3(as shown in FIG. 6); compacting the graphene foam film by adopting a flat press under the pressure of 40MPa to obtain the graphene foam film with the thickness of 71 mu m and the density of 2.19g/cm3The heat conduction coefficient of the graphene heat conduction film is 1760W/m.K. An SEM image of the obtained graphene thermal conductive film is shown in fig. 7.
Example 3:
a preparation method of a graphene film as a medium transmission core in a heat pipe comprises the following steps:
the thickness of the graphene oxide film produced by this company was 70 μm. And (3) reducing the graphene oxide film by flame at 600 ℃ to obtain the flame reduced graphene oxide film with the thickness of 750 mu m. Further performing thermal treatment reduction, heating from room temperature to the maximum temperature of 900 ℃, keeping the temperature for 1h, and heating at a rate of 5 ℃/min to obtain a reduced graphene film with a thickness of 690 mu m and a density of 0.067g/cm3. As shown in fig. 8, is a photograph of the appearance of a sample of graphene film. As shown in fig. 9, is an SEM image of the product graphene film. As shown in FIG. 10, the obtained graphene film is vertically placed in water, and the climbing phenomenon of water in the graphene film is observed, wherein the vertical climbing distance of the water is 85mm, and the graphene film is an excellent capillary wick and can be used as a transmission wick of a medium in a heat pipe.
Comparative example 1:
the oriented self-assembled graphene oxide film produced and manufactured by the company is an original film and has the thickness of 138 mu m; stacking the graphene oxide films in multiple layers, separating the layers by using 150 mu m graphite paper, stacking the layers in a graphite boat, performing thermal reduction, heating to 2850 ℃ from room temperature, keeping the temperature for 1h, heating to 300 ℃ at 0.5 ℃/min, heating to 300-900 ℃ at 3 ℃/min and heating to 900-2850 ℃ at 4 ℃/min to obtain the reduced graphene foam film with the thickness of 348 mu m and the density of 0.22g/cm3(ii) a Compacting the graphene foam film by adopting a roller press under the pressure of 25MPa to obtain the graphene foam film with the thickness of 39 mu m and the density of 1.99g/cm3The thermal conductivity coefficient of the graphene thermal conductive film is 1560W/m.K.
The external surface of the resulting product and the SME pattern are shown in figures 11 and 12. Compared with example 1, the obtained graphene foam has small density and large thickness, and the equipment productivity is seriously influenced.
Comparative example 2:
the oriented self-assembled graphene oxide film produced and manufactured by the company is an original film and has the thickness of 138 mu m; stacking the graphene oxide films, separating each two layers by using graphite paper with the thickness of 300 mu m, stacking the graphene oxide films in a graphite boat, performing thermal reduction, heating to 2900 ℃ from room temperature, keeping the temperature for 1h, and heating to 300 ℃ at the temperature of 0.5 ℃/minHeating at 300-900 ℃ by 3 ℃/min, heating at 900-2900 ℃ by 4 ℃/min to obtain the reduced graphene foam film with the thickness of 621 mu m and the density of 0.25g/cm3(ii) a Compacting the graphene foam film by adopting a roller press under the pressure of 25MPa to obtain the graphene foam film with the thickness of 76 mu m and the density of 2.04g/cm3The heat conduction coefficient of the graphene heat conduction film is 1750W/m.K.
The external surface of the resulting product and the SME pattern are shown in figures 13 and 14. Compared with example 2, the obtained graphene foam has small density and large thickness, and the equipment productivity is seriously influenced.
From the SEM pictures of examples 1 and 2 it is clear that the cavities of the comparative examples are large at the same scale. In the SEM pictures of the products of examples 1 and 2, voids of 5 μm or more were few, whereas in the SEM pictures of the products of comparative examples 1 and 2, voids of 5 μm or more were many. Moreover, the graphene sheets in the embodiments are very close, substantially less than 2 μm, and the graphene sheets are closer in direct proximity. In the SEM image of the comparative example, the graphene layers are far apart from each other.
Finally, it should be noted that: although the present invention has been described in detail with reference to the foregoing embodiments, it will be apparent to those skilled in the art that changes may be made in the embodiments and/or equivalents thereof without departing from the spirit and scope of the invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
Claims (12)
1. A preparation method of a graphene heat conduction film is characterized by comprising the following steps:
reducing the graphene oxide film by adopting a flame firing method;
carrying out first compaction treatment on the graphene oxide subjected to flame reduction treatment;
then carrying out high-temperature thermal reduction; and
a second compaction process is performed.
2. The method for preparing the graphene thermal conductive film according to claim 1, wherein the flame firing heating method is specifically: the graphene oxide film is passed over the flame where it contacts the outer flame of the flame.
3. The method for preparing the graphene thermal conductive film according to claim 2, wherein the temperature of the outer flame of the flame is 300-600 ℃.
4. The method according to claim 3, wherein the temperature of the flame at the outer flame is 400 ± 50 ℃.
5. The method for preparing the graphene thermal conductive film according to claim 2, wherein the passing speed is 0.5-5 m/min.
6. The method for preparing the graphene thermal conductive film according to claim 5, wherein the passing speed is 1-2 m/min.
7. The method for preparing the graphene thermal conductive film according to claim 1, wherein the temperature of the high-temperature thermal reduction is 2000-3000 ℃.
8. The preparation method of the graphene thermal conduction film according to claim 7, wherein the specific method of high-temperature thermal reduction is as follows: placing the reduced graphene oxide film in a pyrogen reduction device, gradually increasing the temperature in the pyrogen reduction device from room temperature to 2000-3000 ℃, wherein the temperature increasing speed is 2-10 ℃/min;
preferably, the temperature in the pyrogen reduction equipment is increased from room temperature to 600 ℃ at the temperature rising speed of 2 ℃/min;
further preferably, the temperature in the pyrogen reduction equipment is increased from 600 ℃ to the final reduction temperature at a temperature rise speed of 4-5 ℃/min.
9. The preparation method of the graphene thermal conductive film according to claim 1, wherein the graphene oxide film after flame reduction is subjected to constant temperature treatment at 2000-3000 ℃ for 45-80 min;
preferably, a plurality of graphene oxide films are stacked together to perform batch graphitization treatment; further preferably, each adjacent photo graphene oxide film is separated by graphite paper.
10. The preparation method of the graphene thermal conductive film according to claim 1, wherein the second compaction treatment is rolling or flat pressing, and the pressure is not less than 20 MPa; the preferable pressure is 25-60 MPa.
11. The preparation method of the graphene thermal conductive film according to any one of claims 1 to 10, wherein the first compaction treatment is rolling or flat pressing, and the pressure is not less than 5 MPa; the preferable pressure is 10-15 MPa.
12. The method for preparing the graphene thermal conductive film according to any one of claims 1 to 10, wherein the graphene oxide film is prepared by dispersing, coating, drying and stripping graphene oxide slurry, and preferably has a thickness of 4 to 300 μm.
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| CN111943178A (en) * | 2020-08-21 | 2020-11-17 | 伊诺福科光学技术有限公司 | Method for preparing graphene material through self-sufficient reduction, graphene material, graphene film, electrode and capacitor |
| CN113501717A (en) * | 2021-07-22 | 2021-10-15 | 常州富烯科技股份有限公司 | Graphite crucible for graphitization furnace and method for preparing graphene heat-conducting film by using graphite crucible |
| CN113371705A (en) * | 2021-07-22 | 2021-09-10 | 常州富烯科技股份有限公司 | Graphite crucible for graphitization furnace and method for preparing graphene heat-conducting film by using graphite crucible |
| CN113371697A (en) * | 2021-07-22 | 2021-09-10 | 常州富烯科技股份有限公司 | Graphite boat and crucible for graphitization furnace and preparation method of graphene heat-conducting film |
| CN113603080A (en) * | 2021-08-25 | 2021-11-05 | 常州富烯科技股份有限公司 | Boat for preparing graphene foam film and method for preparing graphene foam film by using same |
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