阅读说明：本技术 一种高硬度硬涂膜及其制备方法 (High-hardness hard coating film and preparation method thereof ) 是由 张克然 史梦 于 2020-04-30 设计创作，主要内容包括：本发明涉及UV光固化涂料领域,具体涉及一种高硬度硬涂膜及其制备方法。为了解决现有高硬度硬涂膜在涂布硬化涂层的过程中易起皱或卷曲的问题,本发明提供一种高硬度硬涂膜及其制备方法。所述硬涂膜依次包括第一硬涂层、基材和第二硬涂层。本发明提供的高硬度硬涂膜的制造方法包括如下步骤：在基材的一面贴上保护膜a；在未覆保护膜的一面制备得到第一硬涂层；在第一硬涂层表面贴上保护膜b；将保护膜a撕下,在基材的这一面涂布第二硬化涂液,先后经过高压汞灯和UV-LED光源固化后得到第二硬涂层；将硬涂膜在烘箱中进行烘烤。本发明提供的高硬度硬涂膜在涂布硬化涂层的过程,膜面不易起皱或卷曲,且不易翘曲。(The invention relates to the field of UV (ultraviolet) photocureable coatings, in particular to a high-hardness hard coating and a preparation method thereof. The invention provides a high-hardness hard coating film and a preparation method thereof, aiming at solving the problem that the existing high-hardness hard coating film is easy to wrinkle or curl in the process of coating a hardened coating. The hard coating film comprises a first hard coating layer, a base material and a second hard coating layer in sequence. The method for producing a high-hardness hard coating film provided by the invention comprises the following steps: sticking a protective film a on one surface of the base material; preparing a first hard coating on one side which is not covered with the protective film; attaching a protective film b on the surface of the first hard coating; tearing off the protective film a, coating a second hardening coating liquid on one surface of the base material, and curing by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating; and baking the hard coating film in an oven. The high-hardness hard coating provided by the invention has the advantages that the film surface is not easy to wrinkle or curl and is not easy to warp in the process of coating the hard coating.)

1. A high-hardness hard coating film characterized by comprising a first hard coating layer, a substrate and a second hard coating layer in this order.

2. The high-hardness hard coating film according to claim 1, wherein a raw material of the first hard coating layer is first formulated into a first photocurable composition comprising a solvent of methyl ethyl ketone and a solvent of propylene glycol monomethyl ether; the raw materials of the second hard coating layer are firstly prepared into a second light-cured composition, and the second light-cured composition comprises solvent acetone.

3. The high-hardness hardcoat film of claim 1 wherein the raw materials of the first hardcoat layer are first formulated into a first photocurable composition comprising a tetrafunctional urethane acrylate oligomer, pentaerythritol triacrylate, a photoinitiator, a leveling agent, a solvent butanone and a solvent propylene glycol monomethyl ether; the raw materials of the second hard coating are firstly prepared into a second light-cured composition, and the second light-cured composition comprises a nine-functionality-degree polyurethane acrylate oligomer, a three-functionality-degree fluorine-containing butyl acrylate, pentaerythritol triacrylate, a photoinitiator and solvent acetone.

4. The high-hardness hard coating film according to claim 1, wherein the raw material of the first hard coating layer is first formulated into a first photocurable composition comprising the following components: 30-40 parts of tetrafunctional urethane acrylate oligomer, 25-35 parts of polyfunctional active monomer pentaerythritol triacrylate, 0.5-1 part of photoinitiator 184, 0.1-0.3 part of flatting agent BYK-333, 20-25 parts of solvent butanone and 10-15 parts of solvent propylene glycol monomethyl ether; the total parts of the tetrafunctional urethane acrylate oligomer, the multifunctional active monomer pentaerythritol triacrylate, the photoinitiator, the leveling agent, the solvent butanone and the solvent propylene glycol monomethyl ether are 100 parts by weight;

the raw materials of the second hard coating are firstly prepared into a second light-cured composition, and the second light-cured composition comprises the following components: 30-40 parts of nine-functionality-degree polyurethane acrylate oligomer, 20-30 parts of trifunctional fluorine-containing butyl acrylate, 5-15 parts of polyfunctional active monomer pentaerythritol triacrylate, 1-2 parts of photoinitiator 184, 0.1-0.3 part of flatting agent BYK-333 and 23.5-32.8 parts of solvent acetone; the total parts of the nine-functionality polyurethane acrylate oligomer, the three-functionality fluorine-containing butyl acrylate, the multi-functionality active monomer pentaerythritol triacrylate, the photoinitiator, the leveling agent and the solvent acetone are 100 parts by weight.

5. The high-hardness hard coating film according to claim 1, wherein the thickness of the first hard coating layer is 8 to 12 μm.

6. The high-hardness hard coating film according to claim 5, wherein the thickness of the second hard coating layer is 25 to 30 μm.

7. A method for producing a high-hardness hard coating film according to any one of claims 1 to 6, characterized by comprising the steps of:

(1) film coating: sticking a protective film on one surface of the base material;

(2) a first hard coat layer forming step: coating a first hardening coating liquid on the surface, which is not covered with the protective film, of the base material obtained in the step (1), and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a first hard coating;

(3) a film coating step, namely attaching a protective film on the surface of the first hard coating obtained in the step (2);

(4) a second hard coat layer forming step: tearing off the protective film adhered in the step (1) of the structure obtained in the step (3), coating a second hardening coating liquid on the surface of the base material, and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating;

(5) a heat treatment step: and (4) baking the hard coating film obtained in the step (4).

8. The method for producing a high-hardness hard coating film according to claim 7, wherein,

(2) a first hard coat layer forming step: coating a first hardening coating liquid on one surface of the base material obtained in the step (1) which is not covered with the protective film, drying the formed coating in an oven at 80-90 ℃ for 4 minutes, and then curing the dried coating by a high-pressure mercury lamp and a UV-LED light source in sequence;

(4) a second hard coat layer forming step: and (3) tearing off the protective film adhered in the step (1) of the structure obtained in the step (3), coating a second hardening coating liquid on the surface of the base material, drying the formed coating in an oven at the temperature of 80-90 ℃ for 4 minutes, and then curing the dried coating by a high-pressure mercury lamp and a UV-LED light source.

9. The method for producing a high-hardness hard coating film according to claim 7, comprising the steps of:

(1) film coating: sticking a protective film a on one surface of the base material;

(2) a first hard coat layer forming step: coating a first hardening coating liquid on the surface, which is not covered with the protective film a, of the base material obtained in the step (1), and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a first hard coating;

(3) a film coating step, namely attaching a protective film b on the surface of the first hard coating obtained in the step (2);

(4) a second hard coat layer forming step: tearing off the protective film a with the structure obtained in the step (3), coating a second hardening coating liquid on one surface of the base material, and curing by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating;

(5) a heat treatment step: and (4) baking the hard coating film obtained in the step (4) in an oven at a high temperature.

10. The method for producing a hard coating film with high hardness according to any one of claims 7 to 9, wherein in the heat treatment step, the baking temperature is 100-120 ℃ and the baking time is 5 minutes.

Technical Field

The invention relates to the field of UV (ultraviolet) photocureable coatings, in particular to a high-hardness hard coating film with high hardness, high wear resistance and low warpage and a preparation method thereof.

Background

The conventional plastic processing technology has been unable to meet the light and thin requirements of modern products, especially in the field of electronic products such as smart phones, flat computers, etc., the panels of the displays are required to be lighter and thinner. The display window or front panel of these mobile devices is typically made of glass or tempered glass, however glass has the disadvantages of being heavy and vulnerable.

As an alternative to glass, plastic resin films have the property of being lightweight and resistant to impact, which corresponds to the trend of consumers for lighter and thinner mobile devices.

Display windows or front panels of mobile devices generally need to have the characteristics of low warpage, high hardness, high wear resistance and the like, but plastic resin films cannot meet the requirements, surface treatment is needed, and the most common method is to coat a hardened coating on the surface of the plastic resin film. The hardness of the coating is related to the thickness of the coating and the crosslinking density during the curing process of the coating liquid. In order to meet the requirements of mobile devices, a hardened coating (referred to as a hard coating for short) with a high crosslinking density is generally applied to the surface of the plastic resin film in a single layer. The hardened coating layer generates significant hardening shrinkage during curing, which causes wrinkling or curling of the plastic resin film, which is detrimental to the subsequent production process. Therefore, a thick hard coating film is difficult to be used for practical applications.

Disclosure of Invention

The invention provides a high-hardness hard coating film and a preparation method thereof, aiming at solving the problem that the existing high-hardness hard coating film is easy to wrinkle or curl in the process of coating a hardened coating. The high-hardness hard coating provided by the invention has the advantages that the film surface is not easy to wrinkle or curl and is not easy to warp in the process of coating the hard coating.

The invention provides a high-hardness hard coating film which sequentially comprises a first hard coating layer, a base material and a second hard coating layer.

High hardness means a hardness of 9H.

Further, the substrate is a polyethylene terephthalate (PET) film.

Further, the thickness of the first hard coating layer is 8-12 μm.

Further, the thickness of the second hard coating layer is 25-30 μm.

Further, the thickness of the substrate is 75-188 μm.

Further, raw materials of the first hard coating are firstly prepared into a first light-cured composition, and the first light-cured composition comprises solvent butanone and solvent propylene glycol monomethyl ether; the raw materials of the second hard coating layer are firstly prepared into a second light-cured composition, and the second light-cured composition comprises solvent acetone.

Further, raw materials of the first hard coating are firstly prepared into a first photocuring composition, and the first photocuring composition comprises a tetrafunctional polyurethane acrylate oligomer, a polyfunctional active monomer pentaerythritol triacrylate, a photoinitiator, a leveling agent, a solvent butanone and a solvent propylene glycol monomethyl ether; the raw materials of the second hard coating are firstly prepared into a second light-cured composition, and the second light-cured composition comprises a nine-functionality-degree polyurethane acrylate oligomer, a three-functionality-degree fluorine-containing butyl acrylate, a multi-functionality-degree active monomer pentaerythritol triacrylate, a photoinitiator and solvent acetone. The multifunctional reactive monomer pentaerythritol triacrylate is pentaerythritol triacrylate.

Further, raw materials of the first hard coating are firstly prepared into a first photocuring composition, and the first photocuring composition comprises a tetrafunctional polyurethane acrylate oligomer, a polyfunctional active monomer pentaerythritol triacrylate, a photoinitiator, a leveling agent, a solvent butanone and a solvent propylene glycol monomethyl ether; the raw materials of the second hard coating are firstly prepared into a second photocuring composition, and the second photocuring composition comprises a nine-functionality-degree polyurethane acrylate oligomer, a three-functionality-degree fluorine-containing butyl acrylate, a multi-functionality-degree active monomer pentaerythritol triacrylate, a photoinitiator, a leveling agent and solvent acetone.

Further, the raw materials of the first hard coating layer are firstly prepared into a first light-cured composition, and the first light-cured composition comprises the following components: 30-40 parts of tetrafunctional urethane acrylate oligomer, 25-35 parts of polyfunctional active monomer pentaerythritol triacrylate, 0.5-1 part of photoinitiator 184, 0.1-0.3 part of flatting agent BYK-333, 20-25 parts of solvent butanone and 10-15 parts of solvent propylene glycol monomethyl ether; the total parts of the four-functionality polyurethane acrylate oligomer, the multifunctional active monomer pentaerythritol triacrylate, the photoinitiator, the leveling agent, the solvent butanone and the solvent propylene glycol monomethyl ether are 100 parts by weight.

The formula of the first photo-curing composition is abbreviated as formula A, and the first photo-curing composition can also be called as a first hardening coating liquid.

Further, the raw materials of the second hard coating layer are firstly prepared into a second light-cured composition, and the second light-cured composition comprises the following components: 30-40 parts of nine-functionality-degree polyurethane acrylate oligomer, 20-30 parts of trifunctional fluorine-containing butyl acrylate, 5-15 parts of polyfunctional active monomer pentaerythritol triacrylate, 1-2 parts of photoinitiator 184, 0.1-0.3 part of flatting agent BYK-333 and 23.5-32.8 parts of solvent acetone; the total parts of the nine-functionality polyurethane acrylate oligomer, the three-functionality fluorine-containing butyl acrylate, the multi-functionality active monomer pentaerythritol triacrylate, the photoinitiator, the leveling agent and the solvent acetone are 100 parts by weight.

The formula of the second light-cured composition is abbreviated as formula B, and the second light-cured composition can also be called as a second hardening coating liquid.

Further, the raw materials of the first hard coating layer are firstly prepared into a first light-cured composition, and the first light-cured composition comprises the following components: 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. The raw materials of the second hard coating are firstly prepared into a second light-cured composition, and the second light-cured composition comprises the following components: 33 parts by weight of nine-functional polyurethane acrylate oligomer, 25 parts by weight of trifunctional fluorine-containing butyl acrylate, 10 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 1.5 parts by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, and 30.4 parts by weight of solvent acetone. Further, the thickness of the substrate is 100 μm, the thickness of the first hard coating layer is 10 μm, and the thickness of the second hard coating layer is 25 μm.

The invention aims to provide a preparation method, which can prevent a hard coating film from wrinkling or curling when the hard coating film is too thick in the process of coating a hardened coating, promote the hard coating film with high hardness and high wear resistance to be widely used on mobile equipment and achieve the aim of improving the production yield.

The method for producing a high-hardness hard coating film provided by the invention comprises the following steps:

(1) film coating: sticking a protective film on one surface of the base material;

(2) a first hard coat layer forming step: coating a first hardening coating liquid on the surface, which is not covered with the protective film, of the base material obtained in the step (1), and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a first hard coating;

(3) a film coating step, namely attaching a protective film on the surface of the first hard coating obtained in the step (2);

(4) a second hard coat layer forming step: tearing off the protective film adhered in the step (1) of the structure obtained in the step (3), coating a second hardening coating liquid on the surface of the base material, and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating;

(5) a heat treatment step: and (4) baking the hard coating film obtained in the step (4).

Further, the method for producing a high-hardness hard coat film comprises:

(2) a first hard coat layer forming step: coating a first hardening coating liquid on the surface, which is not covered with the protective film, of the base material obtained in the step (1), drying the formed coating in an oven at 80-90 ℃ for 4 minutes, and curing by a high-pressure mercury lamp and a UV-LED light source to obtain a first hard coating;

(4) a second hard coat layer forming step: and (3) tearing off the protective film adhered in the step (1) of the structure obtained in the step (3), coating a second hardening coating liquid on the surface of the base material, drying the formed coating in an oven at the temperature of 80-90 ℃ for 4 minutes, and then curing the dried coating by a high-pressure mercury lamp and a UV-LED light source.

Further, the method for manufacturing the high-hardness hard coating film includes the steps of:

(1) film coating: sticking a protective film a on one surface of the base material;

(2) a first hard coat layer forming step: coating a first hardening coating liquid on the surface, which is not covered with the protective film a, of the base material obtained in the step (1), and curing the base material by a high-pressure mercury lamp and a UV-LED light source to obtain a first hard coating;

(3) a film coating step, namely attaching a protective film b on the surface of the first hard coating obtained in the step (2);

(4) a second hard coat layer forming step: tearing off the protective film a with the structure obtained in the step (3), coating a second hardening coating liquid on one surface of the base material, and curing by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating; (5) a heat treatment step: and (4) baking the hard coating film obtained in the step (4) in an oven at a high temperature.

Further, in the manufacturing method of the high-hardness hard coating film, in the heat treatment step, the baking temperature is 100-120 ℃, and the baking time is 5 minutes.

Further, the method further comprises the following steps:

(6) and a film tearing step of tearing the protective film b from the surface of the first hard coating film.

In the preparation method, the film coating step is used for improving the mechanical strength of the structure so as to avoid wrinkling or curling of the film surface in the curing process of the hardening coating liquid, and the heat treatment step is used for eliminating the internal stress of the hardening coating, reducing the shrinkage of the coating and avoiding the warping of the hardening coating.

Further, the method for producing the hard coat film includes the steps of:

(1) a film covering step, namely attaching a protective film a to one surface of a base material to improve the mechanical strength of the base material;

(2) a first hard coating layer forming step, namely coating a first hardening coating liquid (formula A) on the uncoated surface of the substrate, and curing the first hard coating layer by a high-pressure mercury lamp and a UV-LED light source in sequence to obtain a first hard coating layer;

(3) a film covering step, namely attaching a protective film b on the surface of the first hard coating to improve the mechanical strength of the base material;

(4) a second hard coating forming step of tearing off the protective film a, coating a second hardening coating liquid (formula B) on the surface, and curing the second hard coating liquid by a high-pressure mercury lamp and a UV-LED light source in sequence to obtain a second hard coating;

(5) a heat treatment step, namely baking the hard coating film in an oven at a high temperature of 100 ℃ and 120 ℃ for 5 minutes;

(6) and a film tearing step of tearing the protective film b which plays a supporting role from the surface of the first hard coating film.

The preparation method of the hard coating film provided by the invention has the beneficial effects that: (1) the mechanical strength of the base film is increased through the film coating, and the structure can resist the stress shrinkage of the thick hard coating film caused by coating curing, thereby being beneficial to the subsequent processing of the base film. (2) The invention adds a high-temperature baking process, which eliminates the internal stress of the coating layer generated in the curing process through high-temperature baking, thereby reducing the warping of the hard coating film. (3) The invention can completely cure the thick hardened coating through the use of an efficient solvent system and an efficient UV system, thereby ensuring the high hardness and high wear resistance of the hard coating.

The mechanism of the technical scheme of the invention is as follows:

1. the hard coat film of the present invention is composed of a base material, a first hard coat layer and a second hard coat layer. The protective film A is firstly attached to one side of a base material, and a first hard coating with a dyne value (dyne value is more than 36) is coated on one side of the base material, wherein the first hard coating plays a role in increasing the mechanical strength of the structure and facilitating printing and coating. Before coating the second hard coating with high hardness and high wear resistance, the surface of the first hard coating is coated with a protective film B, and the protective film A is torn off and coated. In order to reduce the warpage of the hard coating film, the invention adds a high-temperature baking process, which eliminates the internal stress of the coating layer generated by the curing process through high-temperature baking, thereby reducing the shrinkage of the coating layer.

2. Efficient solvent system: the invention selects acetone as the solvent of acrylic resin. In the whole coating process, the wet coating liquid can volatilize the solvent in the wet coating liquid through an oven, the surface solvent can be volatilized due to overlarge coating thickness of the ultrahigh-hardness hard coating film, and the solvent in the coating easily causes solvent residue, so that the adhesion and hardness of the coating are seriously influenced. In order to avoid the situation, acetone with high volatilization speed and low boiling point is selected as a solvent.

3. High efficiency UV curing system: the second hard coating layer with ultra-high hardness has an excessive thickness, so that the phenomenon that the surface of the coating layer is cured and the interior of the coating layer is not cured can occur if a traditional UV curing system is adopted, and the adhesion and hardness of the coating layer can be influenced. The invention adopts a mode of combining a high-pressure mercury lamp and a UV-LED light source, firstly uses the high-pressure mercury lamp with strong penetrating power to solidify the inside of the coating, and then uses the UV-LED light source to solidify the whole coating.

Drawings

Fig. 1 is a schematic structural view of a hard coating film provided by the present invention.

Detailed Description

For a better understanding of the present invention, its structure, and the functional features and advantages attained by its structure, reference is made to the following detailed description of the preferred embodiments taken in conjunction with the accompanying drawings, in which:

as shown in fig. 1, the present invention provides a hard coating film comprising a first hard coating layer 1, a substrate 2 and a second hard coating layer 3 in this order.

Further, the preparation method of the hard coating film provided by the invention comprises the following steps: a protective film (a) is stuck to one surface of a base material, a first hard coat liquid is prepared, the first hard coat liquid is applied to the non-film-coated surface of the base material, the formed coating layer is dried at 80 to 90 ℃ for 4 minutes, and then the dried coating layer is cured by ionizing radiation active energy rays (for example, ultraviolet rays) to obtain a first hard coat layer. And attaching a protective film b to the surface of the first hard coating, tearing off the protective film a, preparing a second hardening coating liquid, coating the second hardening coating liquid on the other surface of the base material, drying the formed coating at 80-90 ℃ for 4 minutes, and curing the dried coating by a high-pressure mercury lamp and a UV-LED light source to obtain a second hard coating. And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at a certain temperature (100-.

The performance of the hard coating film provided by the invention is tested according to the following method:

(1) haze, Total light transmittance

Measured by a transmitted light method using a haze meter of the Japanese electrochromic NDH 2000N type.

(2) Hardness of pencil

The pencil hardness of the article was measured using an Elcometer 3086 pencil hardness meter. Measurement method: using a Mitsubishi pencil with the hardness of H-9H, drawing 5 lines under a load of 500g, observing whether the hard coating layer is scratched or not, and judging according to the following standard.

Criteria for determination

Scratching 0-1 strip, and judging Pass;

scratching 2-5 strips, and judging NG (unqualified).

(3) Wear resistance

Using Kunzhijia apparatus A20-339 steel wool tester at 500gf/cm²Under a load of 1kg, the hard coat layer was rubbed 1000 times back and forth with a #0000 steel wool under a load of 1kg, and the presence or absence of scratches was confirmed.

And (3) judging standard:

scratching 0 strips, and judging 'Pass' (qualified);

and (5) scratching more than or equal to 1, and judging NG (unqualified).

(4) Coating thickness test

The thickness of the transparent hardened coating (hard coating) was measured using the optical diffraction principle using a coating thickness gauge ETA-SST thickness measuring system.

(5) Adhesion test

After the coating is scribed by a ruling knife, the coating is pasted by a 3M adhesive tape and then pulled, and the area of the coating which is not pulled is observed by naked eyes and is characterized by percentage.

(6) Warp of

Cutting a 10cm × 10cm sheet, placing the hard coating layer upwards on a horizontal marble platform, testing the four-corner warpage value and recording data, and taking the maximum value. The average value is obtained by measuring 3 slices.

Example 1

The present invention provides a photocurable composition and a hard coat film, as shown in fig. 1, the hard coat film includes a substrate 2 and a hard coat layer including a first hard coat layer 1 and a second hard coat layer 3.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 100 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd., Japan).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-film-coated side of the above-mentioned PET substrate (also referred to as a base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 10 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 33 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.5 parts by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 30.4 parts by weight of a solvent acetone. It was coated onto the other side of the PET substrate described above. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm.

And after the second hard coating is completely cured, placing the hard coating film in an oven, baking for five minutes at the temperature of 110 ℃, and tearing off the protective film b after baking to obtain a final product.

Example 2

The photocurable composition and the method for producing a hard coat film as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of an optical-grade polyethylene terephthalate film (trade name; XG7PL2, manufactured by Toray corporation, Korea) having a thickness of 125 μm.

The formula A is a photocuring composition prepared by mixing 30 parts by weight of tetrafunctional urethane acrylate oligomer, 35 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.6 part by weight of photoinitiator 184, 0.2 part by weight of leveling agent BYK-333, 23 parts by weight of solvent butanone and 11.2 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 9 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 40 parts by weight of a nine-functional urethane acrylate oligomer, 20 parts by weight of a trifunctional butyl fluoroacrylate, 5 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 2 parts by weight of a photoinitiator 184, 0.2 parts by weight of a leveling agent BYK-333, and 32.8 parts by weight of solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 120 ℃, and tearing off the protective film b after baking to obtain the final product.

Example 3

The photocurable composition and the method for producing a hard coat film as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 75 μm thick optical-grade polyethylene terephthalate film (trade name; XG9LA7, manufactured by Toray corporation, Korea).

The formula A is a photocuring composition prepared by mixing 40 parts by weight of tetrafunctional urethane acrylate oligomer, 25 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 1 part by weight of photoinitiator 184, 0.3 part by weight of leveling agent BYK-333, 23.7 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 9 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 30 parts by weight of a nine-functional urethane acrylate oligomer, 30 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1 part by weight of a photoinitiator 184, 0.3 part by weight of a leveling agent BYK-333, and 28.7 parts by weight of solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm.

Example 4

The photocurable composition and the method for producing a hard coat film as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of an optical-grade polyethylene terephthalate film (trade name; XG7PL2, manufactured by Toray corporation, Korea) having a thickness of 188 μm.

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 33 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.8 part by weight of photoinitiator 184, 0.2 part by weight of leveling agent BYK-333, 20 parts by weight of solvent butanone and 11 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 12 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 35 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 15 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1 part by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 23.9 parts by weight of solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by means of a high-pressure mercury lamp and a UV-LED light source in succession, the thickness of the cured coating being 30 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 100 ℃, and tearing off the protective film b after baking to obtain the final product.

Example 5

The photocurable composition and the method for producing a hard coat film as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials, Suzhou) was attached to one surface of a 75 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd.).

The formula A is a photocuring composition prepared by mixing 38 parts by weight of tetrafunctional urethane acrylate oligomer, 32 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 19.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 8 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 37 parts by weight of a nine-functional urethane acrylate oligomer, 26 parts by weight of a trifunctional butyl fluoroacrylate, 12 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.2 parts by weight of a photoinitiator 184, 0.3 parts by weight of a leveling agent BYK-333, and 23.5 parts by weight of a solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 120 ℃, and tearing off the protective film b after baking to obtain the final product.

Comparative example 1

The photocurable composition as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials, Suzhou) was attached to one surface of a 75 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd.).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 8 μm.

After the first hard coating is cured, the protective film a is torn off, and the formula B is a photocuring composition prepared by mixing 33 parts by weight of nine-functionality-degree polyurethane acrylate oligomer, 25 parts by weight of trifunctional fluorine-containing butyl acrylate, 10 parts by weight of multifunctional active monomer pentaerythritol triacrylate, 1.5 parts by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333 and 30.4 parts by weight of solvent acetone. It is applied to the other side of the substrate. After drying the formed coating at 80-90 ℃ for 4 minutes, the dried coating was cured by a UV-LED light source and a high-pressure mercury lamp to a thickness of 25 μm after curing.

And after the second hard coating is completely cured (after light irradiation, the second hard coating is completely cured), placing the hard coating in an oven, baking for five minutes at the temperature of 120 ℃, and obtaining a final product after baking.

Compared with the technical scheme provided by the invention, the manufacturing method of the comparative example 1 is different in that the protective film b is not attached after the first hard coating is cured.

Comparative example 2

The photocurable composition as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 100 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd., Japan).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 10 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared from 33 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.5 parts by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 30.4 parts by weight of solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 150 ℃, and tearing off the protective film b after baking to obtain the final product.

Compared with the technical scheme provided by the invention, the manufacturing method of the comparative example 2 is different in that the temperature of the oven is raised to 150 DEG C

Comparative example 3

The photocurable composition as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 100 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd., Japan).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 9 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 33 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.5 parts by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 30.4 parts by weight of a solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source, the thickness of the cured coating being 25 μm. And (5) tearing off the protective film b to obtain a final product.

Compared with the technical scheme provided by the invention, the manufacturing method of the comparative example 3 is different in that no baking stage is provided.

Comparative example 4

The photocurable composition as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 100 μm optical-grade polyethylene terephthalate film (trade name; O321E, manufactured by Mitsubishi resin Co., Ltd., Japan).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp followed by a UV-LED light source to obtain a first hard coating. The thickness of the first hard coat layer was 8 μm.

After the first hard coat layer was cured, a protective film b (trade name; XY-250C, manufactured by shaoxing source new materials science and technology ltd.) was attached to the surface thereof, and the protective film a was peeled off, and a photocurable composition prepared by mixing 33 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.5 parts by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 30.4 parts by weight of a solvent isopropyl alcohol was applied to the other side of the above-mentioned film (base material). After drying the formed coating at 80-90 ℃ for 4 minutes, the dried coating was cured by means of a high-pressure mercury lamp and a UV-LED light source in succession, the thickness of the cured coating being 25 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 120 ℃, and tearing off the protective film b after baking to obtain the final product.

Compared with the technical scheme provided by the invention, the manufacturing method of the comparative example 4 is different in that the solvent of the formula B is replaced by isopropanol.

Comparative example 5

The photocurable composition as provided in example 1.

A protective film a (trade name; T3603, manufactured by Taylon electronic materials Co., Ltd., Suzhou) was attached to one surface of a 75 μm thick optical-grade polyethylene terephthalate film (trade name; XG9LA7, manufactured by Toray corporation, Korea).

The formula A is a photocuring composition prepared by mixing 35 parts by weight of tetrafunctional urethane acrylate oligomer, 30 parts by weight of polyfunctional active monomer pentaerythritol triacrylate, 0.5 part by weight of photoinitiator 184, 0.1 part by weight of leveling agent BYK-333, 24.4 parts by weight of solvent butanone and 10 parts by weight of solvent propylene glycol monomethyl ether. It is applied to the non-coated side of the above-mentioned substrate (also referred to as base film). After drying the formed coating layer in an oven at 80 to 90 ℃ for 4 minutes, the dried coating layer was cured by a high-pressure mercury lamp to obtain a first hard coating layer. The thickness of the first hard coat layer was 8 μm.

After the first hard coat layer was cured, a protective film B (trade name; XY-250C) was applied to the surface of the first hard coat layer, and formula B was a photocurable composition prepared by mixing 33 parts by weight of a nine-functional urethane acrylate oligomer, 25 parts by weight of a trifunctional butyl fluoroacrylate, 10 parts by weight of a polyfunctional reactive monomer pentaerythritol triacrylate, 1.5 parts by weight of a photoinitiator 184, 0.1 part by weight of a leveling agent BYK-333, and 30.4 parts by weight of a solvent acetone. It is applied to the other side of the substrate. After drying the formed coating in an oven at 80-90 ℃ for 4 minutes, the dried coating was cured by a high pressure mercury lamp, the thickness of the coating after curing being 25 μm.

And after the second hard coating is completely cured, placing the hard coating in an oven, baking for five minutes at the temperature of 120 ℃, and tearing off the protective film b after baking to obtain the final product.

The manufacturing method of comparative example 5 is different from the solution provided by the present invention in that the curing of the second hard coat layer uses only a high pressure mercury lamp.

Table 1 results of performance test of hard coating film provided in example

Table 2 results of performance test of hard coating film provided in comparative example

The hard coating film provided by the invention has good comprehensive performance, and has the performances of high hardness, high wear resistance and low warpage. Among them, the hard coat film provided in example 1 has the best overall properties. Comparative example 1 since the support film was not attached, wrinkles occurred on both sides of the film when the second hard coat layer was applied, so that the hard coat film could not be wound up and the application had to be terminated.

The above description is only a preferred embodiment of the present invention, and is not intended to limit the scope of the present invention. All equivalent changes and modifications made according to the disclosure of the present invention are covered by the scope of the claims of the present invention.