Process method of graphene high-temperature-resistant material

By chemically activate zinc oxide and graphene oxide on graphene materials and adding catalysts to generate composite materials, the problems of graphene stability and conduction properties at high temperatures are solved, and high temperature resistance and high conduction of nano-level composite materials are achieved sex.

CN119144172AInactive Publication Date: 2024-12-17DONGGUAN CHIHANG ENVIRONMENTAL PROTECTION TECH CO LTD
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Patent Information

Application Number
CN202310708872.2
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2023-06-15
Publication Date
2024-12-17
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

At the nanoscale level, graphene materials are difficult to maintain active effects, and there are few researches on functional multi-group interfaces during in-situ reactions, especially under high temperature conditions.

Method used

The chemical activation of nano-grade zinc oxide and graphene oxide is carried out by using sodium tetrapolypropylene benzenesulfonate. The zinc oxide-graphene oxide composite material is added through ultrasonic dissolution and stirring, and the zinc oxide-graphene oxide composite material is improved to improve its Stability and conduction performance.

Benefits of technology

The high temperature and high conductivity of nano-level composite materials are achieved, which enhances the stability of the material and expands the reaction area.

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Abstract

The invention relates to a graphene high-temperature-resistant material process method in the technical field of graphite powder, which comprises the following steps: carrying out chemical activation on nano-scale zinc oxide and graphene oxide by using sodium tetra (polypropylene) benzene sulfonate, and ultrasonically dissolving zinc oxide and graphene oxide in deionized water; adding sodium tetra (polypropylene) benzene sulfonate while stirring; dissolving the activated tin oxide graphene in an organic solution, adding a reducing agent while stirring, and freeze-drying in a refrigerator for a preset time to obtain zinc oxide-graphene oxide sol; and adding a catalyst into the zinc oxide-graphene oxide sol, and reacting to generate the composite material. According to the invention, the nano-scale zinc oxide is loaded on the graphene oxide and is catalytically combined to form the composite material, and the composite material belongs to the nano scale, increases the reaction area, has high temperature resistance and high conductivity, and has good stability.
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Description

Technical Field

[0001] The invention relates to the technical field of graphite powders, in particular to a process method for a graphene high temperature resistant material. Background Art

[0002] At present, there are many studies on the three-dimensional (3D) forms of graphene nanomaterials such as aerogels, microporous or mesoporous frameworks and hydrogels generated by reactions. Graphene or graphene oxide, both of which contain π in the monoatomic layer flow, has been identified as a good modifier. Graphene or graphene oxide combined with elastomeric structures can add a variety of functional characteristics. Loading nanoscale metals on graphene can exhibit different functions in the electronic or magnetic fields. In previous studies, there have been studies on dissolved or dissolved graphene, such as nanodispersion. However, there are few reports on the study of functional multi-component interfaces during in situ reactions because monomers are difficult to distribute at the nanoscale level and the active effect cannot be well maintained. Summary of the invention

[0003] The purpose of the present invention is to solve the above defects and provide a process method for graphene high temperature resistant material.

[0004] In order to solve the above technical problems, the present invention adopts the following technical solution: a graphene high temperature resistant material process method, comprising the following steps:

[0005] S1, using sodium tetrapropylene benzene sulfonate to chemically activate nano-scale zinc oxide and graphene oxide, dissolving zinc oxide and graphene oxide in deionized water by ultrasonic, and adding sodium tetrapropylene benzene sulfonate while stirring;

[0006] S2, dissolving the activated tin oxide graphene in an organic solution, adding a reducing agent while stirring, and placing the solution in a refrigerator for freeze drying for a predetermined time to obtain a zinc oxide-graphene oxide sol;

[0007] S3, adding a catalyst into the zinc oxide-graphene oxide sol to react and generate a composite material.

[0008] Furthermore, the stirring speed in S1 is 10-16000 r / min.

[0009] Furthermore, the content of sodium tetrapropylene benzene sulfonate is 2% to 5% by weight of the mixed solution of zinc oxide particles and graphene oxide.

[0010] Further, under the conditions of a temperature of 80 to 100° C., a stirring speed of 20 to 9000 r / min, and a stirring time of 2 to 90 h, the activated graphene oxide nanosheets are dissolved in polyoxypropylene glycol, and stirred until the solution becomes viscous.

[0011] Furthermore, the reducing agent in S2 is a mixed solution of N2H4·H2O and NH3·H2O, and the molar ratio of N2H4·H2O to NH3·H2O is 1:(4-6).

[0012] Furthermore, the catalyst of S3 is toluene diisocyanate oligomer.

[0013] The beneficial effects of the present invention are as follows:

[0014] Compared with the prior art, the present invention loads nanometer-level zinc oxide on graphene oxide to catalytically combine into a composite material. The composite material is nanometer-level, increases the reaction area, has the performance of high temperature resistance and high conductivity, and has good stability. DETAILED DESCRIPTION

[0015] The present invention is further described in detail below in conjunction with specific implementation modes.

[0016] A graphene high temperature resistant material process method comprises the following steps:

[0017] S1, using sodium tetrapropylene benzene sulfonate to chemically activate nano-scale zinc oxide and graphene oxide, dissolving zinc oxide and graphene oxide in deionized water by ultrasonic, and adding sodium tetrapropylene benzene sulfonate while stirring;

[0018] S2, dissolving the activated tin oxide graphene in an organic solution, adding a reducing agent while stirring, and placing the solution in a refrigerator for freeze drying for a predetermined time to obtain a zinc oxide-graphene oxide sol;

[0019] S3, adding a catalyst into the zinc oxide-graphene oxide sol to react and generate a composite material.

[0020] The stirring speed in S1 is 10-16000 r / min.

[0021] The content of sodium tetrapropylene benzene sulfonate is 2% to 5% by weight of the mixed solution of zinc oxide particles and graphene oxide.

[0022] Under the conditions of temperature of 80-100° C., stirring speed of 20-9000 r / min, and stirring time of 2-90 h, the activated graphene oxide nanosheets are dissolved in polyoxypropylene glycol, and stirred until the solution becomes viscous.

[0023] The reducing agent in the S2 is a mixed solution of N2H4·H2O and NH3·H2O, and the molar ratio of N2H4·H2O to NH3·H2O is 1:(4-6).

[0024] The catalyst of S3 is toluene diisocyanate oligomer.

[0025] The present invention loads nanometer-level zinc oxide on graphene oxide to catalytically combine into a composite material. The composite material is nanometer-level, increases the reaction area, has the performance of high temperature resistance and high conductivity, and has good stability.

[0026] The above description is only a preferred embodiment of the present invention and does not limit the present invention in any form. Although the present invention is disclosed as a preferred embodiment as above, it is not used to limit the present invention. Any technician familiar with the profession can make some changes or modifications to equivalent embodiments of equivalent changes by using the technical contents disclosed above without departing from the scope of the technical solution of the present invention. However, any simple modification, equivalent changes and modifications made to the above embodiments according to the technology of the present invention are within the scope of the technical solution of the present invention without departing from the content of the technical solution of the present invention.

Claims

1. A graphene high temperature resistant material process method, Features: The following steps are involved: S1, using sodium tetrapropylene benzene sulfonate to chemically activate nano-scale zinc oxide and graphene oxide, dissolving zinc oxide and graphene oxide in deionized water by ultrasonic, and adding sodium tetrapropylene benzene sulfonate while stirring; S2, dissolving the activated tin oxide graphene in an organic solution, adding a reducing agent while stirring, and placing the solution in a refrigerator for freeze drying for a predetermined time to obtain a zinc oxide-graphene oxide sol; S3, adding a catalyst into the zinc oxide-graphene oxide sol to react and generate a composite material.

2. A graphene high temperature resistant material process according to claim 1, Features: The stirring speed in S1 is 10-16000 r / min.

3. A graphene high temperature resistant material process according to claim 1, Features: The content of sodium tetrapropylene benzene sulfonate is 2% to 5% by weight of the mixed solution of zinc oxide particles and graphene oxide.

4. A graphene high temperature resistant material process according to claim 1, Features: Under the conditions of temperature of 80-100° C., stirring speed of 20-9000 r / min, and stirring time of 2-90 h, the activated graphene oxide nanosheets are dissolved in polyoxypropylene glycol, and stirred until the solution becomes viscous.

5. A graphene high temperature resistant material process according to claim 1, Features: The reducing agent in the S2 is a mixed solution of N2H4·H2O and NH3·H2O, and the molar ratio of N2H4·H2O to NH3·H2O is 1:(4-6).

6. A graphene high temperature resistant material process according to claim 1, Features: The catalyst of S3 is toluene diisocyanate oligomer.