阅读说明：本技术 一种含原位聚合绝缘涂层的碳纳米管电热膜的制备方法 (Preparation method of carbon nano tube electrothermal film containing in-situ polymerization insulating coating ) 是由 刘海龙 钱涛 马迪 于 2020-12-30 设计创作，主要内容包括：本发明涉及高分子材料领域,公开了一种含原位聚合绝缘涂层的碳纳米管电热膜的制备方法。本发明首先通过将碳纳米管强制分散在有机溶剂中,然后加入正硅酸四乙酯、硅烷偶联剂和羟基树脂对其进行改性,避免团聚,再将改性后的碳纳米管分散液置于聚四氟乙烯滤膜表面抽滤、干燥、剥离,得到改性碳纳米管薄膜,再将偏苯三酸酐和二异氰酸酯制备得到的聚酰胺酰亚胺预聚体加入,在改性碳纳米管薄膜表面原位聚合得到聚酰胺酰亚胺绝缘层；实现了聚酰胺酰亚胺绝缘材料在电热膜上的应用。该绝缘层耐热性能好,不易老化,且通过原位聚合的方式与电热膜复合,贴合度好,无需外加胶黏剂。(The invention relates to the field of high polymer materials, and discloses a preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating. The preparation method comprises the steps of firstly, forcibly dispersing carbon nanotubes in an organic solvent, then adding tetraethyl orthosilicate, a silane coupling agent and hydroxyl resin to modify the carbon nanotubes to avoid agglomeration, placing the modified carbon nanotube dispersion liquid on the surface of a polytetrafluoroethylene filter membrane for suction filtration, drying and stripping to obtain a modified carbon nanotube film, adding a polyamide-imide prepolymer prepared from trimellitic anhydride and diisocyanate, and carrying out in-situ polymerization on the surface of the modified carbon nanotube film to obtain a polyamide-imide insulating layer; the application of the polyamide-imide insulating material to the electrothermal film is realized. The insulating layer is good in heat resistance, not easy to age, good in fitting degree and free of additional adhesive, and is compounded with the electrothermal film in an in-situ polymerization mode.)

1. A preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating is characterized by comprising the following steps:

1) preparing a carbon nano tube film: adding the carbon nano tube into an organic solvent, shearing and stirring at a high speed for 20-40min at the rotation speed of 4000-6000rpm, then adding ammonia water and water, slowly dropwise adding a mixed solution of tetraethyl orthosilicate, a silane coupling agent and hydroxyl resin, and continuing stirring and reacting for 1-2h after dropwise adding is finished for 1-2 h; then placing the modified carbon nano tube dispersion liquid in a suction filtration device containing a polytetrafluoroethylene filter membrane, carrying out vacuum suction filtration for 3-4h, then drying at 70-90 ℃ for 3-4h, taking out the polytetrafluoroethylene filter membrane, soaking in absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain a modified carbon nano tube film;

2) preparing an insulating coating: dissolving trimellitic anhydride in N-methyl pyrrolidone, adding diisocyanate, heating to 120-.

2. The method of claim 1, wherein: the thickness of the modified carbon nanotube film is 35-50 μm; the thickness of the polyamide-imide insulating layer is 10-25 mu m.

3. The method of claim 1, wherein: in step 1): the organic solvent is selected from one or more of absolute ethyl alcohol, isopropanol and sec-butyl alcohol; the hydroxyl resin is selected from one or more of hydroxyl polyester resin and hydroxyl acrylic resin with the hydroxyl value of 80-120mg KOH/g.

4. The method of claim 1, wherein: in step 1): the silane coupling agent is one or more selected from gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, beta- (3, 4-epoxycyclohexyl) -ethyl trimethoxy silane, gamma-aminopropyl triethoxy silane and N-beta- (aminoethyl) -gamma-aminopropyl trimethoxy silane.

5. The method according to any one of claims 1 to 4, wherein: in step 1): the mass ratio of the carbon nano tube, the organic solvent, the ammonia water, the tetraethyl orthosilicate, the silane coupling agent and the hydroxyl resin is 2-5:20-40:2-5:20-40:10-20:1-5: 10-20.

6. The method of claim 1, wherein: in step 2): the diisocyanate is selected from one or more of diphenylmethane-4, 3' -diisocyanate, toluene diisocyanate, p-phenylene diisocyanate and 3,3' -dimethyl-4, 3' -biphenyl diisocyanate.

7. The method of claim 1, wherein: in step 2): the blocking agent is selected from phenol and p-chlorophenol.

8. The production method according to claim 6 or 7, characterized in that: in step 2): the molar ratio of the trimellitic anhydride to the diisocyanate is 1: 1-1.02.

9. The method of claim 8, wherein: in step 2): the mass of the N-methyl pyrrolidone is 2-3 times of the total mass of the trimellitic anhydride and the diisocyanate.

10. The method of claim 7, wherein: in step 2): the mass of the blocking agent is 2-5wt% of diisocyanate.

Technical Field

The invention relates to the field of high polymer materials, in particular to a preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating.

Background

The electrothermal film is a novel electric heating technology which is developed rapidly in recent years, the electrothermal film is used as a heating element, heat energy can be generated after the electrothermal film is electrified, and the heat enters the surrounding space in a radiation mode. Compared with the traditional mode of utilizing the electric heating wire to give off heat for the energization of the resistance element, the electric heating wire does not need secondary heat conduction when in use, the heating is quick and uniform, the use is safe and convenient, the heat energy utilization rate can reach more than 95 percent, and the electric heating wire is a clean and efficient heating mode. The electrothermal film can be divided into a metal electrothermal film and a nonmetal electrothermal film according to the materials used by the electrothermal film, wherein the carbon-based electrothermal film is the most common nonmetal electrothermal film.

The carbon nanotube is a seamless nanomaterial formed by winding a single-layer or multi-layer graphite sheet layer around the same central axis according to a specific helical angle. The carbon nano tube has the structural characteristics of low density, high length-diameter ratio, high graphitization degree and the like, has high mechanical strength and good electrical conductivity and thermal conductivity, can be used as a composite material reinforcing material, and can be used for transparent conductive films due to good electrical conductivity and high visible light transmittance after film forming. The carbon nano tube has excellent flexibility, light weight, quick heating and easy processing, and becomes a research hotspot in the field of electrothermal films; it can be said that carbon nanotubes are an almost ideal electrical heating material. However, the carbon nanotube has a large specific surface area, is easy to agglomerate, has a poor interface effect when being combined with other materials, can hardly be uniformly dispersed in any solvent, and has poor uniformity of a prepared film.

The electric heat membrane both sides are insulating layer and decorative layer respectively, and wherein the decorative layer is heated by the electric heat membrane as the outmost of electric heat membrane, directly gives off the heat with the radiant heat mode, and the insulating layer can prevent that the heat from losing to the opposite side with heat-conduction mode, also prevents simultaneously that the electric leakage is dangerous. The common insulating layer adopts a flame-retardant polyester film, has limited heat resistance and is easy to age, the common insulating layer can be compounded with the electrothermal film through an adhesive, and the traditional adhesive is easy to heat and age, so that the insulating layer is easy to fall off.

The polyamide-imide is a thermoplastic resin with flexible amide groups and heat-resistant imide rings regularly arranged, has certain flexibility, excellent high-temperature resistance, dielectric property and insulating property, has outstanding bonding property on metal and other materials, and is widely applied to the fields of aerospace, electronics, fire protection, wire enamel and the like as a high-temperature-resistant insulating coating. The polyamide-imide is an ideal insulating layer material, but the polyamide-imide cannot be used as a base film material like PET (polyethylene terephthalate) polyester and is bonded with a carbon material film to form an electrothermal film, so that no literature report is found for applying the polyamide-imide to the electrothermal film.

Disclosure of Invention

In order to solve the technical problem, the invention provides a preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating. The preparation method comprises the steps of firstly, forcibly dispersing carbon nanotubes in an organic solvent, then adding tetraethyl orthosilicate and a silane coupling agent to modify the carbon nanotubes to avoid agglomeration, placing modified carbon nanotube dispersion liquid on the surface of a polytetrafluoroethylene filter membrane for suction filtration, drying and stripping to obtain a modified carbon nanotube film, adding a polyamide-imide prepolymer prepared from trimellitic anhydride and diisocyanate, and carrying out in-situ polymerization on the surface of the modified carbon nanotube film to obtain a polyamide-imide insulating layer; the application of the polyamide-imide insulating material to the electrothermal film is realized. The insulating layer is good in heat resistance, not easy to age, good in fitting degree and free of additional adhesive, and is compounded with the electrothermal film in an in-situ polymerization mode.

The specific technical scheme of the invention is as follows:

a preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating comprises the following steps:

1) preparing a carbon nano tube film: adding the carbon nano tube into an organic solvent, shearing and stirring at a high speed for 20-40min at the rotation speed of 4000-6000rpm, then adding ammonia water and water, slowly dropwise adding a mixed solution of tetraethyl orthosilicate, a silane coupling agent and hydroxyl resin, and continuing stirring and reacting for 1-2h after dropwise adding is finished for 1-2 h; and then placing the modified carbon nano tube dispersion liquid in a suction filtration device containing a polytetrafluoroethylene filter membrane, carrying out vacuum suction filtration for 3-4h, then drying for 3-4h at 70-90 ℃, taking out the polytetrafluoroethylene filter membrane, soaking in absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain the modified carbon nano tube film.

2) Preparing an insulating coating: dissolving trimellitic anhydride in N-methyl pyrrolidone, adding diisocyanate, heating to 120-.

The technical principle of the invention is as follows:

in the step 1), the carbon nano tube is modified by tetraethyl orthosilicate and a silane coupling agent, so that the carbon nano tube is uniformly dispersed in an organic solvent to avoid agglomeration, then a carbon nano tube film is prepared by a vacuum filtration method, the modified carbon nano tube dispersion liquid is deposited on a polytetrafluoroethylene microporous filter membrane, and the carbon nano tube film is obtained by peeling after drying. The invention can improve the dispersibility of the carbon nano tube by carrying out hydrolysis-condensation reaction on tetraethyl orthosilicate and a silane coupling agent under the catalysis of ammonia water, and simultaneously can play a role of a bonding agent due to rich silicon hydroxyl and amino/epoxy functional groups, and can react with isocyanate groups in the subsequent in-situ polymerization process to uniformly and firmly bond the polyamide-imide insulating layer on the carbon nano tube film.

In the step 2), the reaction product of trimellitic anhydride and diisocyanate is sealed by a sealing agent, the obtained polyamide-imide prepolymer has low molecular weight, and in the in-situ polymerization process, the temperature is raised to the deblocking temperature, the sealing agent is removed, the isocyanate group is regenerated, the self-crosslinking curing reaction is carried out, and the reaction with the silicon hydroxyl group and the amino/epoxy functional group on the surface of the carbon nano tube is carried out, so that the polyamide-imide prepolymer is firmly combined on the surface of the carbon nano tube film.

Preferably, the thickness of the modified carbon nanotube film is 35-50 μm; the thickness of the polyamide-imide insulating layer is 10-25 mu m.

Preferably, in step 1): the organic solvent is selected from one or more of absolute ethyl alcohol, isopropanol and sec-butyl alcohol.

Preferably, in step 1): the hydroxyl resin is selected from one or more of hydroxyl polyester resin and hydroxyl acrylic resin with the hydroxyl value of 80-120mg KOH/g.

Preferably, in step 1): the silane coupling agent is one or more selected from gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, beta- (3, 4-epoxycyclohexyl) -ethyl trimethoxy silane, gamma-aminopropyl triethoxy silane and N-beta- (aminoethyl) -gamma-aminopropyl trimethoxy silane.

Preferably, in step 1): the mass ratio of the carbon nano tube, the organic solvent, the ammonia water, the tetraethyl orthosilicate, the silane coupling agent and the hydroxyl resin is 2-5:20-40:10-20:1-5: 10-20.

Preferably, in step 2): the diisocyanate is selected from one or more of diphenylmethane-4, 3' -diisocyanate, toluene diisocyanate, p-phenylene diisocyanate and 3,3' -dimethyl-4, 3' -biphenyl diisocyanate.

Preferably, in step 2): the blocking agent is selected from phenol and p-chlorophenol.

Preferably, in step 2): the molar ratio of the trimellitic anhydride to the diisocyanate is 1: 1-1.02.

Preferably, in step 2): the mass of the N-methyl pyrrolidone is 2-3 times of the total mass of the trimellitic anhydride and the diisocyanate.

Preferably, in step 2): the mass of the blocking agent is 2-5wt% of diisocyanate.

Compared with the prior art, the invention has the following technical effects:

1. the invention modifies the carbon nano tube by tetraethyl orthosilicate and silane coupling agent, avoids the agglomeration of the carbon nano tube, and then prepares the carbon nano tube film by a vacuum filtration method, the thickness of the film is controllable, and the defects of uniformity are few.

2. The tetraethyl orthosilicate and the silane coupling agent added in the invention still have rich silicon hydroxyl and amino/epoxy active functional groups after hydrolysis-condensation, and high hydroxyl resin is introduced to endow the carbon nano tube with excellent flexibility.

3. According to the invention, the isocyanate group of the polyamide-imide is sealed by the phenol sealing agent, so that the obtained polyamide-imide prepolymer regenerates the isocyanate group after reaching the deblocking temperature, and reacts with the hydroxyl, silicon hydroxyl and amino/epoxy active functional groups on the surface of the carbon nanotube during the in-situ polymerization reaction, and the adhesive is not required to be added, so that the adhesion degree is good.

4. The synthesis method is simple and easy to industrialize, and the prepared carbon nano tube electrothermal film can be applied to low-voltage electrothermal products.

Detailed Description

The present invention will be further described with reference to the following examples.

General examples

A preparation method of a carbon nano tube electrothermal film containing an in-situ polymerization insulating coating comprises the following steps:

1) preparing a carbon nano tube film: adding carbon nano tubes into an organic solvent, shearing and stirring at a high speed for 20-40min at the rotation speed of 4000-.

Wherein the organic solvent is selected from absolute ethyl alcohol, isopropanol and sec-butyl alcohol. The hydroxyl resin is selected from hydroxyl polyester resin and hydroxyl acrylic resin, and the hydroxyl value is 80-120mg KOH/g. The silane coupling agent is selected from gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, beta- (3, 4-epoxycyclohexyl) -ethyl trimethoxy silane, gamma-aminopropyl triethoxy silane and N-beta- (aminoethyl) -gamma-aminopropyl trimethoxy silane. The mass ratio of the carbon nano tube, the organic solvent, the ammonia water, the tetraethyl orthosilicate, the silane coupling agent and the hydroxyl resin is 2-5:20-40:10-20:1-5: 10-20.

2) Preparing an insulating coating: dissolving trimellitic anhydride in N-methylpyrrolidone, adding diisocyanate, heating to 120-.

Wherein the diisocyanate is selected from diphenylmethane-4, 3' -diisocyanate, toluene diisocyanate, p-phenylene diisocyanate, and 3,3' -dimethyl-4, 3' -biphenyl diisocyanate. The blocking agent is selected from phenol and p-chlorophenol. The molar ratio of the trimellitic anhydride to the diisocyanate is 1: 1-1.02. The mass of the N-methyl pyrrolidone is 2 to 3 times of the total mass of the trimellitic anhydride and the diisocyanate. The mass of the blocking agent is 2-5wt% of diisocyanate.

Example 1

1) Preparing a carbon nano tube film: adding carbon nanotubes into isopropanol, shearing and stirring at a high speed for 20min, rotating at the speed of 4000rpm, then adding ammonia water and water, then slowly dropwise adding a mixed solution of tetraethyl orthosilicate, gamma- (2, 3-epoxypropoxy) propyltrimethoxysilane and hydroxyl polyester resin with the hydroxyl value of 80mg KOH/g, finishing dropwise adding for 1h, continuously stirring and reacting for 2h, then placing the modified carbon nanotube dispersion solution into a Buchner funnel of a polytetrafluoroethylene filter membrane, carrying out suction filtration for 3h, then drying at 70 ℃ for 4h, taking out the polytetrafluoroethylene filter membrane, soaking in absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain a modified carbon nanotube film with the thickness of 35 mu m; the mass ratio of the carbon nano tube, the isopropanol, the ammonia water, the tetraethyl orthosilicate, the gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane to the hydroxyl polyester resin is 2: 20: 3: 20: 10: 1: 10;

2) preparing an insulating coating: dissolving trimellitic anhydride in N-methyl pyrrolidone, adding diphenylmethane-4, 3' -diisocyanate, heating to 120 ℃, carrying out heat preservation reaction for 3 hours, adding phenol, carrying out heat preservation reaction for 1 hour to obtain a polyamide imide prepolymer, uniformly coating the polyamide imide prepolymer on a modified carbon nanotube film, heating to 180 ℃, carrying out heat preservation reaction for 2 hours to unseal the polyamide imide prepolymer, carrying out in-situ polymerization reaction on the surface layer of the modified carbon nanotube film to obtain an in-situ polymerized insulating coating on the surface of the carbon nanotube electrothermal film, wherein the thickness of the insulating coating is 25 micrometers; the molar ratio of trimellitic anhydride to diphenylmethane-4, 4 ' -diisocyanate was 1:1, the mass of N-methylpyrrolidone was 3 times the total mass of trimellitic anhydride and diphenylmethane-4, 4 ' -diisocyanate, and the mass of phenol was 2 wt% of diphenylmethane-4, 4 ' -diisocyanate.

Example 2

1) Preparing a carbon nano tube film: adding carbon nanotubes into absolute ethyl alcohol, shearing and stirring at a high speed for 40min, rotating at the speed of 6000rpm, then adding ammonia water and water, then slowly dropwise adding a mixed solution of tetraethyl orthosilicate, beta- (3, 4-epoxycyclohexyl) -ethyltrimethoxysilane and hydroxyl acrylic resin with the hydroxyl value of 120mg KOH/g, finishing dropwise adding for 2h, continuously stirring and reacting for 1h, then placing the modified carbon nanotube dispersion solution into a Buchner funnel of a polytetrafluoroethylene filter membrane, carrying out suction filtration for 4h, then drying at 90 ℃ for 3h, taking out the polytetrafluoroethylene filter membrane, soaking in the absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain a modified carbon nanotube film with the thickness of 50 mu m; the mass ratio of the carbon nano tube, the absolute ethyl alcohol, the ammonia water, the tetraethyl orthosilicate, the beta- (3, 4 epoxycyclohexyl) -ethyl trimethoxy silane hydroxyl value to the hydroxyl acrylic resin is 5: 40: 20: 3: 20;

2) preparing an insulating coating: dissolving trimellitic anhydride in N-methyl pyrrolidone, adding toluene diisocyanate, heating to 140 ℃, carrying out heat preservation reaction for 2 hours, adding p-chlorophenol, carrying out heat preservation reaction for 2 hours to obtain a polyamide imide prepolymer, uniformly coating the polyamide imide prepolymer on a modified carbon nanotube film, heating to 200 ℃, carrying out heat preservation reaction for 1 hour to unseal the polyamide imide prepolymer, carrying out in-situ polymerization reaction on the surface layer of the modified carbon nanotube film to obtain an in-situ polymerized insulating coating on the surface of the carbon nanotube electrothermal film, wherein the thickness of the insulating coating is 10 microns; the molar ratio of trimellitic anhydride to toluene diisocyanate is 1: 1.02, the mass of N-methyl pyrrolidone is 2 times of the total mass of trimellitic anhydride and toluene diisocyanate, and the mass of p-chlorophenol is 5wt% of toluene diisocyanate.

Example 3

1) Preparing a carbon nano tube film: adding carbon nano tubes into sec-butyl alcohol, shearing and stirring at a high speed for 30min, rotating at the speed of 5000rpm, then adding ammonia water and water, then slowly dropwise adding a mixed solution of tetraethyl orthosilicate, gamma-aminopropyltriethoxysilane and hydroxyl acrylic resin with the hydroxyl value of 100mg KOH/g, finishing dropwise adding for 1h, continuing stirring and reacting for 2h, then placing the modified carbon nano tube dispersion liquid into a Buchner funnel of a polytetrafluoroethylene filter membrane, carrying out suction filtration for 3h, then drying at the temperature of 80 ℃ for 3h, taking out the polytetrafluoroethylene filter membrane, soaking in absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain a modified carbon nano tube film with the thickness of 40 mu m; the mass ratio of the carbon nano tube, the sec-butyl alcohol, the ammonia water, the tetraethyl orthosilicate, the gamma-aminopropyltriethoxysilane to the hydroxyl acrylic resin is 3: 40: 5: 40: 20: 5: 15.

2) Preparing an insulating coating: dissolving trimellitic anhydride in N-methyl pyrrolidone, adding p-phenylene diisocyanate, heating to 130 ℃, carrying out heat preservation reaction for 3 hours, adding phenol, carrying out heat preservation reaction for 1 hour to obtain a polyamide imide prepolymer, uniformly coating the polyamide imide prepolymer on a modified carbon nanotube film, heating to 180 ℃, carrying out heat preservation reaction for 2 hours to unseal the polyamide imide prepolymer, carrying out in-situ polymerization reaction on the surface layer of the modified carbon nanotube film to obtain an in-situ polymerized insulating coating on the surface of the carbon nanotube film, wherein the thickness of the insulating coating is 20 microns; the molar ratio of the trimellitic anhydride to the p-phenylene diisocyanate is 1: 1.01, the mass of the N-methyl pyrrolidone is 2 times of the total mass of the trimellitic anhydride and the p-phenylene diisocyanate, and the mass of the phenol is 3 wt% of the p-phenylene diisocyanate.

Example 4

1) Preparing a carbon nano tube film: adding carbon nanotubes into isopropanol, shearing and stirring at a high speed for 40min at the rotation speed of 4000rpm, then adding ammonia water and water, then slowly dropwise adding a mixed solution of tetraethyl orthosilicate, N-beta- (aminoethyl) -gamma-aminopropyltrimethoxysilane and hydroxyl polyester resin with the hydroxyl value of 100mg KOH/g, finishing dropwise adding for 2h, continuing stirring and reacting for 1h, then placing the modified carbon nanotube dispersion solution into a Buchner funnel of a polytetrafluoroethylene filter membrane, carrying out suction filtration for 4h, then drying at 70 ℃ for 4h, taking out the polytetrafluoroethylene filter membrane, soaking in absolute ethyl alcohol, mechanically stripping, and drying at room temperature to obtain a modified carbon nanotube film with the thickness of 45 mu m; the mass ratio of the carbon nano tube, the isopropanol, the ammonia water, the tetraethyl orthosilicate, the N-beta- (aminoethyl) -gamma-aminopropyltrimethoxysilane and the hydroxyl polyester resin is 2: 30: 3: 30: 15: 2: 15.

2) Preparing an insulating coating: dissolving trimellitic anhydride in N-methylpyrrolidone, adding 3,3 '-dimethyl-4, 3' -biphenyl diisocyanate, heating to 140 ℃, carrying out heat preservation reaction for 2 hours, adding parachlorophenol, continuing to carry out heat preservation reaction for 1 hour to obtain a polyamide imide prepolymer, uniformly coating the polyamide imide prepolymer on a modified carbon nanotube film, heating to 200 ℃, carrying out heat preservation reaction for 1 hour to unseal the polyamide imide prepolymer, and carrying out in-situ polymerization reaction on the surface layer of the modified carbon nanotube film to obtain an in-situ polymerized insulating coating on the surface of the carbon nanotube electrothermal film, wherein the thickness of the insulating coating is 15 mu m; the molar ratio of trimellitic anhydride to 3,3 '-dimethyl-4, 4' -biphenyl diisocyanate was 1:1, the mass of N-methylpyrrolidone was 3 times the total mass of trimellitic anhydride and 3,3 '-dimethyl-4, 4' -biphenyl diisocyanate, and the mass of p-chlorophenol was 5wt% of 3,3 '-dimethyl-4, 4' -biphenyl diisocyanate.

Comparative example 1

The only difference from example 1 is that no hydroxy resin was added in step 1), the remaining steps and materials and composition were identical to example 1.

Comparative example 2

The only difference from example 1 is that no blocking agent phenol was added in step 2), and the rest of the steps and the materials and compositions were identical to example 1.

Comparative example 3

The carbon nanotube film prepared in step 1) of example 1 is used as an electrothermal film, and commercially available PET is used as an insulating layer and is adhered to the carbon nanotube film by a heat-resistant adhesive.

The thickness of the electric heating film prepared in the embodiments 1 to 4 and the comparative examples 1 to 3 is controlled to be 60 micrometers, and the tensile strength, the thermal stability, the electric heating conversion efficiency, the temperature uniformity and the electric heating stability of the electric heating film are detected, wherein the tensile strength is measured by cutting the electric heating film into samples with the thickness of 60 x 20mm, after reinforcing the two ends of the samples, an electronic universal testing machine is adopted to test the tensile performance of the samples, and the tensile speed is 0.5 mm/min; the thermal stability is judged by the initial thermal decomposition temperature obtained by thermogravimetric analysis test; the electrothermal conversion efficiency is calculated by measuring the electric power consumed by increasing the unit temperature, and the calculation formula is h_r+c＝I_c·V_i/(T_m-T_i)，h_r+cFor the electrothermal conversion efficiency (mW/DEG C), I_cIs a steady state current (mA), V_iFor applying the voltage (V), the test voltage is set to 36V, T_iInitial temperature (. degree. C.), T_mTo stabilize the maximum temperature(. degree. C.); the temperature uniformity is tested by an infrared thermal imager to test the sample temperature of 3 different positions after the electric heating film is electrified, the temperature difference is less than or equal to 1 ℃, the temperature uniformity is excellent, the temperature difference is good at 1-3 ℃, and the temperature difference is greater than 3 ℃; the electric heating stability is judged by measuring the temperature difference at the same position at the same time and the same time after circularly testing for 30 times of temperature rise and fall changes, the temperature difference is less than or equal to 1 ℃, the temperature uniformity is excellent, the temperature difference is good at 1-3 ℃, and the temperature difference is poor at more than 3 ℃; the results are shown in Table 1.

Table 1 examples 1-4 and comparative examples 1-3 product performance test results:

through inspection, the comparative example 1 takes tetraethyl orthosilicate and a silane coupling agent as modifiers, can stably disperse carbon nanotubes, does not add hydroxyl resin, and although active functional groups can connect a polyamide imide layer and a carbon nanotube film, the composite layer is poor in flexibility, the flexibility of an electrothermal film is insufficient, and the tensile strength and the electrothermal conversion efficiency are also reduced to a certain extent; comparative example 2 no blocking agent phenol was added, and the polyamideimide coated on the modified carbon nanotube film was polymerized, and could not be polymerized in situ, the adhesion was not good, the insulating layer was not uniform, the void phenomenon, the tensile strength, the electric-to-thermal conversion efficiency, the temperature uniformity and the electric-to-thermal stability were poor; comparative example 3 a conventional polyester insulating layer was generally used, and the adhesive and the carbon nanotube film were compounded, so that the tensile strength, the electrothermal conversion efficiency and the temperature uniformity were good, but the initial thermal decomposition temperature was decreased more, and the electrothermal stability was also poor, indicating that the heat resistance and the aging resistance of the polyester insulating layer were poor.

The carbon nanotube electrothermal films prepared in the embodiments 1 to 4 have high electrothermal conversion efficiency and good temperature uniformity, and the thermal stability and the electrothermal stability are superior to those of conventional polyester insulating layers, which means that through the connection of silicon hydroxyl and amino/epoxy, the polyamide imide polymerized in situ after deblocking can generate a firmly combined insulating layer on the surface of the carbon nanotube film, no additional adhesive is required, and the degree of adhesion is good.

The raw materials and equipment used in the invention are common raw materials and equipment in the field if not specified; the methods used in the present invention are conventional in the art unless otherwise specified.

The above description is only a preferred embodiment of the present invention, and is not intended to limit the present invention, and all simple modifications, alterations and equivalents of the above embodiments according to the technical spirit of the present invention are still within the protection scope of the technical solution of the present invention.