阅读说明：本技术 一种泡棉材料、用于amoled模组减震的超薄减震泡棉材料层、组件及制备方法 (Foam material, ultrathin damping foam material layer for AMOLED module damping, assembly and preparation method ) 是由 张长星 苏炎召 于 2021-09-06 设计创作，主要内容包括：本发明公开了一种泡棉材料、用于AMOLED模组减震的超薄减震泡棉材料层、组件及制备方法,所述泡棉材料是由成膜聚合物制备而成的内部带有泡孔结构的泡体材料,所述泡体材料的密度为0.4～0.9克/立方厘米；所述泡体材料在10-30℃温度区间内具有不低于0.4的损耗因子；所述成膜聚合物的玻璃化转变温度Tg为(-10)-30℃,且所述成膜聚合物由至少两种或两种以上的Tg差异大于50℃的不同单体共聚而成。本发明制备的泡棉材料能够吸收冲击力,具有优越抗冲击性,利用此特性作为缓冲材料能够广泛使用在手机,平板,笔电,车载以及穿戴设备。(The invention discloses a foam material, an ultrathin damping foam material layer for damping an AMOLED module, a component and a preparation method, wherein the foam material is a foam body material which is prepared from a film-forming polymer and has a foam pore structure inside, and the density of the foam body material is 0.4-0.9 g/cubic centimeter; the foam body material has a loss factor not less than 0.4 within a temperature range of 10-30 ℃; the glass transition temperature Tg of the film-forming polymer is (-10) -30 ℃, and the film-forming polymer is formed by copolymerizing at least two or more different monomers with Tg difference larger than 50 ℃. The foam material prepared by the invention can absorb impact force, has excellent impact resistance, and can be widely used as a buffer material in mobile phones, flat panels, pen-on-board devices, vehicle-mounted devices and wearable devices by utilizing the characteristic.)

1. The foam material is characterized by being a foam body material which is prepared from a film-forming polymer and has a foam pore structure inside, wherein the density of the foam body material is 0.4-0.9 g/cubic centimeter;

the foam body material has a loss factor not less than 0.4 within a temperature range of 10-30 ℃;

the glass transition temperature Tg of the film-forming polymer is (-10) -30 ℃, and the film-forming polymer is formed by copolymerizing at least two or more different monomers with Tg difference larger than 50 ℃.

2. The foam material according to claim 1, wherein the film-forming polymer is a copolymer having a core-shell coating structure;

the core-shell coating structure of the copolymer is a copolymer taking one of polyacrylate-acrylonitrile copolymer, polybutadiene-acrylonitrile/acrylate copolymer, polyacrylate-styrene copolymer or polybutadiene-styrene/acrylate copolymer as a core and one of glassy polymers such as polystyrene-acrylonitrile copolymer, polymethyl methacrylate, poly isobornyl acrylate and the like as a shell.

3. The foam material according to claim 2, wherein the core in the core-shell coating structure is a polyacrylate copolymer with a glass transition temperature not higher than 30 ℃, the polyacrylate copolymer is prepared by emulsifying an acrylate monomer and a monomer containing an unsaturated carbon-carbon double bond by a first emulsifier and copolymerizing by an initiator initiated emulsion polymerization process, and the acrylate monomer is an alkyl acrylate with a structure represented by the following formula (1):

CH₂＝CH-COOR，

formula (1)

Wherein R is an alkane segment with a carbon number of 2-10;

the monomer containing unsaturated carbon-carbon double bonds is one or more of butadiene, styrene and acrylonitrile;

the first emulsifier is one of sodium dodecyl sulfate and sodium dodecyl benzene sulfonate;

the initiator is persulfate initiator;

the shell in the core-shell coating structure is formed by emulsifying a monomer containing unsaturated carbon-carbon double bonds and having a glass transition temperature of not less than 50 ℃ by an anionic emulsifier and a nonionic emulsifier and initiating emulsion polymerization by an initiator, wherein the monomer is selected from one or more of styrene, acrylonitrile, methyl methacrylate or isobornyl acrylate;

the anionic emulsifier is one of sodium dodecyl sulfate, sodium dodecyl benzene sulfonate and other anionic emulsifiers;

the non-ionic emulsifier is one of non-ionic emulsifiers such as nonylphenol polyoxyethylene ether and sorbitan fatty acid ester;

the initiator is persulfate initiator.

4. The foam material according to claim 3, wherein the core in the core-shell coating structure is a polyacrylate copolymer with a glass transition temperature not higher than 20 ℃, and R in formula (1) is an alkane chain segment with 4-10 carbon atoms;

the shell in the core-shell coating structure is formed by polymerizing unsaturated carbon-carbon double bond-containing monomers with the glass transition temperature of not lower than 60 ℃.

5. Foam material according to claim 4,

the core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 10 ℃, and the shell in the core-shell coating structure is formed by polymerizing a monomer containing unsaturated carbon-carbon double bonds with the glass transition temperature not lower than 80 ℃.

6. The foam material as claimed in claim 1, wherein the cell structure has a closed cell structure with a pore size of 5 to 200 μm; the total volume of the foam cell structure accounts for 20-50% of the volume of the whole foam.

7. The foam material according to claim 1, wherein the ultrathin foam material has a loss factor of not less than 0.4 at a temperature range of 5-35 ℃;

the glass transition temperature of the film-forming polymer is 0-20 ℃;

the cellular structure is a closed cell structure;

the pore diameter of the closed cell structure is 20-80 microns, and the total volume of the cell structure accounts for 25-40% of the volume of the whole foam.

8. The foam material according to claim 1, wherein the ultrathin foam material is added with a conductive filler, the conductive filler is 1-20 wt% of the ultrathin foam material, and the conductive filler is one or more of carbon nanotubes, conductive nickel powder, nickel-plated glass fiber and conductive carbon powder.

9. The foam material of claim 8, wherein the conductive filler is 3-10% wt of the ultra-thin foam material.

10. The foam material of claim 8, wherein the ultra-thin foam material has a surface resistivity of 1x10³-1×10⁹The volume resistance of the damping foam is not higher than 1x10 per square ohm⁶Ohm.

11. An ultrathin damping foam material layer for damping an AMOLED module, which is prepared from the foam material in any one of claims 1-10, wherein the ultrathin damping foam material layer is 0.07-0.4mm thick.

12. An ultrathin foam material assembly for damping an AMOLED module, comprising the ultrathin damping foam layer and a release film layer in claim 11, wherein the ultrathin damping foam layer and the release film layer are bonded through a glue layer.

13. The ultra-thin foam assembly for AMOLED module shock absorption according to claim 12, wherein a non-release film layer is disposed between the shock absorbing foam layer and the glue layer.

14. The method for preparing the ultrathin foam material assembly for AMOLED module shock absorption according to claim 12, comprising the following steps:

s1, synthesis of acrylate copolymer seed emulsion:

adding a monomer containing unsaturated carbon-carbon double bonds, a first emulsifier and deionized water into a reaction kettle, heating to 45-55 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 25-35 minutes, keeping a reaction device under the protection of nitrogen, dissolving an initiator in distilled water, dropwise adding the initiator into a reaction solution, heating to 70-80 ℃, and continuously stirring for reacting for 3-4 hours to obtain a prepolymer emulsion A; the weight ratio of the unsaturated carbon-carbon double bond monomer, the first emulsifier, the initiator and the deionized water is 40-60 parts/0.5-5 parts/0.05-0.1 part/40-60 parts.

Then uniformly mixing 10-50 parts by mass of alkyl acrylate shown in the formula (1), 0.05-0.1 part by mass of initiator, 0.5-5 parts by mass of emulsifier and 10-50 parts by mass of deionized water with the prepolymer emulsion A, and reacting at 70-80 ℃ for 3-4 hours to obtain seed emulsion B, wherein the seed emulsion B is the core emulsion in the core-shell coating structure;

s2 preparation of film-forming polymer emulsion

Adding deionized water, a monomer containing unsaturated carbon-carbon double bonds, an anionic emulsifier and a non-ionic emulsifier into a reactor, and stirring and pre-emulsifying to obtain a pre-emulsion C; the weight ratio of the unsaturated carbon-carbon double bond-containing monomer to the anionic emulsifier to the nonionic emulsifier to the deionized water is 40-60 parts/0.3-3 parts/40-60 parts;

then taking 100 parts by mass of the emulsion B prepared in the step S1 as a seed emulsion, synchronously dropwise adding 10-50 parts by mass of the emulsion C and 0.05-0.1 part by mass of an initiator, reacting for 3-6 hours at 70-90 ℃, cooling and discharging to obtain a film-forming polymer emulsion with a core-shell structure;

s3, preparation of a foam material dispersion liquid:

adding the hollow polyacrylonitrile copolymer expanded microspheres, the film-forming polymer emulsion prepared in the step S2, the color paste, the defoaming agent and the wetting agent into a mixing container, and stirring for 10-30 minutes at a low speed by using a stirring paddle until a uniform dispersion liquid is formed for later use, wherein the dispersion liquid is a foam material dispersion liquid containing the core-shell structure copolymer emulsion;

the expanded microspheres, the film-forming polymer emulsion prepared in the step S1, the color paste, the defoaming agent and the wetting agent are 0.5 to 2.5 parts/95 to 99 parts/0.3 to 0.7 part/0.05 to 0.2 part/0.5 to 2 parts by weight;

s4, preparing a foam material:

and (4) uniformly stirring and mixing the dispersion liquid prepared in the step S3, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the release film coated with the wet glue into an oven at 90 ℃ for drying for 10 minutes, and taking out the release film to obtain the ultrathin foam assembly.

Technical Field

The invention relates to compressible ultrathin damping foam, in particular to a foam material, an ultrathin damping foam material layer prepared from the foam material and used for AMOLED module damping, an ultrathin foam component containing the ultrathin damping foam material layer, and a preparation method of the ultrathin foam component.

Background

With the development of science and technology, people cannot live with electronic display devices such as mobile phones, computers and the like. Due to the numerous advantages of the AMOLED, the application range of the AMOLED technology is wider than that of the LCD technology, and the AMOLED technology can be extended to the fields of electronic products, businesses, transportation, industrial control and medical use. Electronic equipment is easy to collide and fall in the using process or the transportation process, so that a layer of buffering material foam (such as PE foam, EVA foam and PU foam) is required to be adhered below the AMOLED screen frame of the electronic equipment and used for absorbing the impact force of the outside on the electronic equipment. However, the traditional foam materials such as PU foam, PE foam, acrylic foam and EVA foam are difficult to meet the requirements of AMOLED, such as higher energy absorption, shock absorption and high impact resistance.

CN111072847A discloses a polyacrylate foam composition and a preparation method thereof. In the embodiment, the polyacrylate synthesized has better falling ball impact resistance after being prepared into foam compared with low glass transition temperature at a certain (relatively higher) glass transition temperature, but the polyacrylate foam composition contains an organic solvent, which is not beneficial to environmental protection. In addition, the polyacrylate foam composition adopted only in the invention has higher glass transition temperature and is not suitable for damping and shock absorption application under the condition of lower temperature.

CN112300524 discloses a high-elasticity acrylic foam, a preparation method and application thereof. The high-elasticity acrylic foam comprises acrylic monomers, natural rubber, foaming microspheres and other auxiliaries, the effect of dual elasticity is expected to be achieved by introducing the rubber and the foaming microspheres, the high-elasticity acrylic foam has good impact resistance, but an organic solvent is used in the preparation method of the high-elasticity acrylic foam, and the preparation method is not beneficial to environmental protection.

CN112680139 discloses acrylic foaming damping foam and a preparation method thereof. The acrylic damping foam can be applied to OLED modules. The formula of the organic solvent type acrylic foam coating liquid is disclosed.

In order to obtain a thin uniform foam material with the best shock absorption and impact resistance and use an environment-friendly production process, influencing factors in the foam material are deeply researched and an optimized material formula and an optimized production process are found.

Disclosure of Invention

Therefore, the foam material provided by the invention has high impact resistance, and when the foam material is used for the shock-absorbing ultrathin foam component of the AMOLED module, the ultrathin foam component has high impact resistance.

The invention also provides an ultrathin damping foam material layer prepared from the ultrathin foam and used for damping the AMOLED module;

further, the invention also provides an ultrathin foam material component for damping the AMOLED module and a preparation method thereof.

In order to solve the technical problems, the invention adopts the following technical scheme:

a foam material is a foam material which is prepared from a film-forming polymer and has a foam structure inside, and the density of the foam material is 0.4-0.9 g/cubic centimeter;

the foam body material has a loss factor not less than 0.4 within a temperature range of 10-30 ℃;

the glass transition temperature Tg of the film-forming polymer is (-10) -30 ℃, and the film-forming polymer is formed by copolymerizing at least two or more different monomers with Tg difference larger than 50 ℃.

The film-forming polymer is a copolymer with a core-shell coating structure;

the core-shell coating structure of the copolymer is a copolymer taking one of polyacrylate-acrylonitrile copolymer, polybutylene-acrylonitrile/acrylate copolymer, polyacrylate-styrene copolymer or polybutadiene-styrene/acrylate copolymer as a core and one of glassy polymers such as polystyrene-acrylonitrile copolymer, polymethyl methacrylate, poly isobornyl acrylate and the like as a shell.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 30 ℃, the polyacrylate copolymer is prepared by emulsifying an acrylate monomer and a monomer containing unsaturated carbon-carbon double bonds through a first emulsifier and initiating emulsion polymerization process copolymerization through an initiator, and the acrylate monomer is alkyl acrylate with the structure shown in the following formula (1):

CH₂＝CH-COOR，

formula (1)

Wherein R is an alkane segment with a carbon number of 2-10;

the monomer containing unsaturated carbon-carbon double bonds is one or more of butadiene, styrene and acrylonitrile;

the first emulsifier is one of sodium dodecyl sulfate and sodium dodecyl benzene sulfonate;

the initiator is persulfate initiator; the persulfate initiator is preferably ammonium persulfate.

The shell in the core-shell coating structure is formed by emulsifying a monomer containing unsaturated carbon-carbon double bonds and having a glass transition temperature of not less than 50 ℃ by an anionic emulsifier and a nonionic emulsifier and initiating emulsion polymerization by an initiator, wherein the monomer is selected from one or more of styrene, acrylonitrile, methyl methacrylate or isobornyl acrylate;

the anionic emulsifier is one of sodium dodecyl sulfate, sodium dodecyl benzene sulfonate and other anionic emulsifiers;

the non-ionic emulsifier is one of non-ionic emulsifiers such as nonylphenol polyoxyethylene ether and sorbitan fatty acid ester;

the initiator is a persulfate initiator, and the persulfate initiator is preferably ammonium persulfate.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 20 ℃, and R in the formula (1) is an alkane chain segment with the carbon atom number of 4-10;

the shell in the core-shell coating structure is formed by polymerizing unsaturated carbon-carbon double bond-containing monomers with the glass transition temperature of not lower than 60 ℃.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 10 ℃, and the shell in the core-shell coating structure is formed by polymerizing a monomer containing unsaturated carbon-carbon double bonds with the glass transition temperature not lower than 80 ℃.

The pore diameter of the cellular structure is a closed cell structure of 5-200 microns; the proportion of the total volume of the cellular structure to the volume of the whole foam is 20-50%.

The ultrathin foam material has a loss factor not less than 0.4 within a temperature range of 5-35 ℃;

the glass transition temperature of the film-forming polymer is 0-20 ℃;

the cellular structure is a closed cell structure;

the pore diameter of the closed cell structure is 20-80 microns, and the proportion of the total volume of the closed cell structure to the volume of the whole foam is 25-40%.

The ultrathin foam material is added with a conductive filler, the conductive filler is 1-20 wt% of the ultrathin foam material, and the conductive filler is one or more of a carbon nano tube, conductive nickel powder, nickel-plated glass fiber and conductive carbon powder.

The conductive filler accounts for 3-10 wt% of the ultrathin foam material.

The surface resistivity of the ultrathin foam material is 1x10³-1x10⁹The volume resistance of the damping foam is not higher than 1x10 per ohm per square⁶Ohm.

The ultrathin damping foam material layer for the AMOLED module is prepared from the foam material, and the thickness of the ultrathin damping foam material layer is 0.07-0.4 mm.

The utility model provides a cotton material subassembly of ultra-thin bubble for AMOLED module shock attenuation, includes the right the cotton layer of ultra-thin shock attenuation bubble with leave type rete, the cotton layer of ultra-thin shock attenuation bubble with leave type rete and pass through the glue film bonding.

And a non-release film layer is arranged between the damping foam layer and the adhesive layer.

The preparation method of the ultrathin foam material component for AMOLED module shock absorption is characterized by comprising the following steps:

s1, synthesis of acrylate copolymer seed emulsion:

adding a monomer containing unsaturated carbon-carbon double bonds, a first emulsifier and deionized water into a reaction kettle, heating to 45-55 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 25-35 minutes, keeping a reaction device under the protection of nitrogen, dissolving an initiator in distilled water, dropwise adding the initiator into a reaction solution, heating to 70-80 ℃, and continuously stirring for reacting for 3-4 hours to obtain a prepolymer emulsion A; the weight ratio of the unsaturated carbon-carbon double bond monomer, the first emulsifier, the initiator and the deionized water is 40-60 parts/0.5-5 parts/0.05-0.1 part/40-60 parts.

Then uniformly mixing 10-50 parts by mass of alkyl acrylate shown in the formula (1), 0.05-0.1 part by mass of initiator, 0.5-5 parts by mass of emulsifier and 10-50 parts by mass of deionized water with the prepolymer emulsion A, and reacting at 70-80 ℃ for 3-4 hours to obtain seed emulsion B, wherein the seed emulsion B is the core emulsion in the core-shell coating structure;

s2 preparation of film-forming polymer emulsion

Adding deionized water, a monomer containing unsaturated carbon-carbon double bonds, an anionic type anionic emulsifier and a nonionic type nonionic emulsifier into a reactor, and stirring and pre-emulsifying to obtain a pre-emulsion C; the weight ratio of the unsaturated carbon-carbon double bond-containing monomer to the anionic emulsifier to the nonionic emulsifier to the deionized water is 40-60 parts/0.3-3 parts/40-60 parts;

then taking 100 parts by mass of the emulsion B prepared in the step S1 as a seed emulsion, synchronously dropwise adding 10-50 parts by mass of the emulsion C and 0.05-0.1 part by mass of an initiator, reacting for 3-6 hours at 70-90 ℃, cooling and discharging to obtain a film-forming polymer emulsion with a core-shell structure;

s3, preparation of a foam material dispersion liquid:

adding the hollow polyacrylonitrile copolymer expanded microspheres, the film-forming polymer emulsion prepared in the step S2, the color paste, the defoaming agent and the wetting agent into a mixing container, and stirring for 10-30 minutes at a low speed by using a stirring paddle until a uniform dispersion liquid is formed for later use, wherein the dispersion liquid is a foam material dispersion liquid containing the core-shell structure copolymer emulsion;

the expanded microsphere, the film-forming polymer emulsion prepared in the step S1, the color paste, the defoaming agent and the wetting agent are 0.5 to 2.5 parts/95 to 99 parts/0.3 to 0.7 part/0.05 to 0.2 part/0.5 to 2 parts by weight.

S4, preparing a foam material:

and (4) uniformly stirring and mixing the dispersion liquid prepared in the step S3, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the release film coated with the wet glue into an oven at 90 ℃ for drying for 10 minutes, and taking out the release film to obtain the ultrathin foam assembly.

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

the foam material provided by the invention is a foam body material which is prepared from a film-forming polymer and internally provided with a cell structure, the cells of the cell structure are subjected to physical or chemical foaming to obtain a closed cell structure, and the pore diameter of the closed cell structure is 5-200 microns. The closed-cell structure foam provides compressibility for the foam, and when the foam is extruded by external force, the foam can deform, and due to the closed-cell structure, part of energy can be absorbed in the deformation resisting process of the foam, so that better damping effect can be provided more favorably than the foam with the open-cell structure. The proportion of the total volume of the cellular structure to the volume of the whole foam is 10-60%, preferably, the proportion of the total volume of the cellular structure to the volume of the whole foam is 20-50%, more preferably, the proportion of the total volume of the cellular structure to the volume of the whole foam is 25-40%. If the volume occupied by the foam holes is too small, the foam holes are difficult to compress, and the assembly of the OLED screen is not facilitated; if the volume occupied by the foam holes is too large, the damping effect of the foam is obviously reduced.

The film-forming polymer has a polyacrylate copolymer with a core-shell coating structure, wherein the core-shell coating structure of the polyacrylate copolymer is a copolymer taking one of polyacrylate-acrylonitrile copolymer, polybutadiene-acrylonitrile/acrylate copolymer, polyacrylate-styrene copolymer or polybutylene-styrene/acrylate copolymer as a core and one of glassy polymers such as polystyrene-acrylonitrile copolymer, polymethyl methacrylate, poly isobornyl acrylate or polystyrene as a shell. The copolymer with the core-shell structure has a wider glass transition temperature, can show excellent damping loss in a wider temperature range, and improves the damping effect of the material.

In the preparation process of the ultrathin foam material, an anionic emulsifier and nonionic emulsifier composite emulsification system is adopted in the step S2. The emulsion stability of the core-shell structure adopted by the invention is easy to cause problems, a composite emulsification system of an anionic emulsifier and a nonionic emulsifier is used, the anionic emulsifier enables particles to be dispersed and stabilized by double effects of a double electric layer and shielding stabilization, and the nonionic emulsifier increases the emulsion stability by shielding stabilization; meanwhile, the charge stability of the anionic emulsifier and the steric hindrance effect of the nonionic emulsifier can generate a synergistic effect, and the stability of emulsion particles is improved.

Drawings

In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, and it is obvious that the drawings in the following description are some embodiments of the present invention, and other drawings can be obtained by those skilled in the art without creative efforts.

FIG. 1 is a schematic view of a structure of a damping foam layer provided by the present invention

FIG. 2 is a schematic view of a first embodiment of the ultra-thin foam set provided by the present invention;

fig. 3 is a schematic diagram of the state of cells of the ultrathin foam provided by the invention after compression.

1-ultrathin damping foam layer, 2-release film layer, 3-adhesive layer, 4-cellular structure, 5-non-release film layer and 6-conductive filler.

Detailed Description

The technical solutions of the present invention will be described clearly and completely with reference to the accompanying drawings, and it should be understood that the described embodiments are some, but not all embodiments of the present invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

The invention provides a foam material, which is a foam material with a foam pore structure inside and prepared from a film-forming polymer, wherein the density of the foam material is 0.4-0.9 g/cubic centimeter;

the foam body material has a loss factor not less than 0.4 within a temperature range of 10-30 ℃;

the glass transition temperature Tg of the film-forming polymer is (-10) -30 ℃, and the film-forming polymer is formed by copolymerizing at least two or more different monomers with Tg difference larger than 50 ℃.

The film-forming polymer is a copolymer with a core-shell coating structure;

the core-shell coating structure of the copolymer is a copolymer taking one of polyacrylate-acrylonitrile copolymer, polybutylene-acrylonitrile/acrylate copolymer, polyacrylate-styrene copolymer or polybutadiene-styrene/acrylate copolymer as a core and one of glassy polymers such as polystyrene-acrylonitrile copolymer, polymethyl methacrylate, poly isobornyl acrylate and the like as a shell.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 30 ℃, the polyacrylate copolymer is prepared by emulsifying an acrylate monomer and a monomer containing unsaturated carbon-carbon double bonds through a first emulsifier and initiating emulsion polymerization process copolymerization through an initiator, and the acrylate monomer is alkyl acrylate with the structure shown in the following formula (1):

CH₂＝CH-COOR，

formula (1)

Wherein R is an alkane segment with a carbon number of 2-10;

the monomer containing unsaturated carbon-carbon double bonds is one or more of butadiene, styrene and acrylonitrile;

the first emulsifier is one of sodium dodecyl sulfate and sodium dodecyl benzene sulfonate;

the initiator is persulfate initiator; the persulfate initiator is preferably ammonium persulfate.

The shell in the core-shell coating structure is formed by emulsifying a monomer containing unsaturated carbon-carbon double bonds and having a glass transition temperature of not less than 50 ℃ by an anionic emulsifier and a nonionic emulsifier and initiating emulsion polymerization by an initiator, wherein the monomer is selected from one or more of styrene, acrylonitrile, methyl methacrylate or isobornyl acrylate;

the anionic emulsifier is one of sodium dodecyl sulfate, sodium dodecyl benzene sulfonate and other anionic emulsifiers;

the non-ionic emulsifier is one of non-ionic emulsifiers such as nonylphenol polyoxyethylene ether and sorbitan fatty acid ester;

the initiator is a persulfate initiator, and the persulfate initiator is preferably ammonium persulfate.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 20 ℃, and R in the formula (1) is an alkane chain segment with the carbon atom number of 4-10;

the shell in the core-shell coating structure is formed by polymerizing unsaturated carbon-carbon double bond-containing monomers with the glass transition temperature of not lower than 60 ℃.

The core in the core-shell coating structure is a polyacrylate copolymer with the glass transition temperature not higher than 10 ℃, and the shell in the core-shell coating structure is formed by polymerizing a monomer containing unsaturated carbon-carbon double bonds with the glass transition temperature not lower than 80 ℃.

The pore diameter of the cellular structure is a closed cell structure of 5-200 microns; the proportion of the total volume of the cellular structure to the volume of the whole foam is 20-50%.

The ultrathin foam material has a loss factor not less than 0.4 within a temperature range of 5-35 ℃;

the glass transition temperature of the film-forming polymer is 0-20 ℃;

the cellular structure is a closed cell structure;

the pore diameter of the closed cell structure is 20-80 microns, and the proportion of the total volume of the closed cell structure to the volume of the whole foam is 25-40%.

The ultrathin foam material is added with a conductive filler, the conductive filler is 1-20 wt% of the ultrathin foam material, and the conductive filler is one or more of a carbon nano tube, conductive nickel powder, nickel-plated glass fiber and conductive carbon powder.

The conductive filler accounts for 3-10 wt% of the ultrathin foam material.

The surface resistivity of the ultrathin foam material is 1x10³-1x10⁹The volume resistance of the damping foam is not higher than 1x10 per ohm per square⁶Ohm.

The ultrathin damping foam material layer for the AMOLED module is prepared from the foam material, and the thickness of the ultrathin damping foam material layer is 0.07-0.4 mm.

As shown in fig. 1, the ultrathin foam material assembly for AMOLED module damping provided by the invention comprises an ultrathin foam damping layer 1 and a release film layer 2, wherein the ultrathin foam damping layer and the release film layer are bonded by a glue layer 3. Preferably, a PET non-release film layer 5 is arranged between the damping foam layer and the adhesive layer. The ultrathin foam material layer is prepared from the foam material, and the thickness of the ultrathin damping foam layer is 0.07-0.4 mm. The foam material is a foam body material which is prepared from a film-forming polymer and internally provided with a foam cell structure 4, and the foam cell structure is a closed cell structure;

as another embodiment, as shown in fig. 2, a conductive filler 6 may be optionally added to the ultrathin foam material provided by the present invention, where the conductive filler 6 is 1-20 wt% of the ultrathin foam material, and the conductive filler is one or more of carbon nanotubes, conductive nickel powder, nickel-plated glass fiber, and conductive carbon powder.

The preparation method of the ultrathin foam material component for AMOLED module shock absorption is characterized by comprising the following steps:

s1, synthesis of acrylate copolymer seed emulsion:

adding a monomer containing unsaturated carbon-carbon double bonds, a first emulsifier and deionized water into a reaction kettle, heating to 45-55 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 25-35 minutes, keeping a reaction device under the protection of nitrogen, dissolving an initiator in distilled water, dropwise adding the initiator into a reaction solution, heating to 70-80 ℃, and continuously stirring for reacting for 3-4 hours to obtain a prepolymer emulsion A; the weight ratio of the unsaturated carbon-carbon double bond monomer, the first emulsifier, the initiator and the deionized water is 40-60 parts/0.5-5 parts/0.05-0.1 part/40-60 parts.

Then uniformly mixing 10-50 parts by mass of alkyl acrylate shown in the formula (1), 0.05-0.1 part by mass of initiator, 0.5-5 parts by mass of emulsifier and 10-50 parts by mass of deionized water with the prepolymer emulsion A, and reacting at 70-80 ℃ for 3-4 hours to obtain seed emulsion B, wherein the seed emulsion B is the core emulsion in the core-shell coating structure;

s2 preparation of film-forming polymer emulsion

Adding deionized water, a monomer containing unsaturated carbon-carbon double bonds, an anionic type anionic emulsifier and a nonionic type nonionic emulsifier into a reactor, and stirring and pre-emulsifying to obtain a pre-emulsion C; the weight ratio of the unsaturated carbon-carbon double bond-containing monomer to the anionic emulsifier to the nonionic emulsifier to the deionized water is 40-60 parts/0.3-3 parts/40-60 parts;

then taking 100 parts by mass of the emulsion B prepared in the step S1 as a seed emulsion, synchronously dropwise adding 10-50 parts by mass of the emulsion C and 0.05-0.1 part by mass of an initiator, reacting for 3-6 hours at 70-90 ℃, cooling and discharging to obtain a film-forming polymer emulsion with a core-shell structure;

s3, preparation of a foam material dispersion liquid:

adding the hollow polyacrylonitrile copolymer expanded microspheres, the film-forming polymer emulsion prepared in the step S2, the color paste, the defoaming agent and the wetting agent into a mixing container, and stirring for 10-30 minutes at a low speed by using a stirring paddle until a uniform dispersion liquid is formed for later use, wherein the dispersion liquid is a foam material dispersion liquid containing the core-shell structure copolymer emulsion;

the expanded microsphere, the film-forming polymer emulsion prepared in the step S1, the color paste, the defoaming agent and the wetting agent are 0.5 to 2.5 parts/95 to 99 parts/0.3 to 0.7 part/0.05 to 0.2 part/0.5 to 2 parts by weight.

S4, preparing a foam material:

and (4) uniformly stirring and mixing the dispersion liquid prepared in the step S3, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the release film coated with the wet glue into an oven at 90 ℃ for drying for 10 minutes, and taking out the release film to obtain the ultrathin foam assembly.

The storage modulus and loss modulus of the material at different temperatures are determined by DMA in the present invention, which is the prior art, and the loss factor can be calculated by "loss factor ═ loss modulus ÷ storage modulus". For example, under the condition of using a constant frequency of 1Hz, a DMA test is carried out at a temperature rise rate of 2 ℃ per minute, the temperature is raised from minus 50 ℃ to 100 ℃, the change conditions of the storage modulus and the loss modulus along with the temperature are measured, and the loss factor is calculated through a formula.

Through detection, the pressure required when the thickness of the damping foam layer provided by the invention is compressed to 25% is not more than 1 MPa.

The film-forming polymer may be selected from polyacrylates and copolymers thereof, polyolefins and copolymers thereof or polyurethanes and copolymers thereof. Further, the film-forming polymer is preferably a polyacrylate copolymer having a core-shell structure and prepared by an emulsion polymerization method. The core is generally composed of components with excellent impact resistance and damping performance, such as polybutadiene-styrene copolymer, poly (n-butyl acrylate) -styrene copolymer or polybutadiene-styrene/acrylate copolymer; the shell covering the shell is made of polymers in glass state, such as polystyrene-acrylonitrile copolymer. The finally obtained core-shell structure latex particles have excellent damping performance. Compatibility between the core-shell two components needs to be considered when the raw material monomer is selected, the better the compatibility is, the higher the mixing range of the molecular chain is, the boundary of the core-shell structure tends to be fuzzy, and the total damping performance also rises correspondingly. The polymerization process of the film-forming polymer is also very important for forming a specific damping microstructure, and a latex interpenetrating polymer network is synthesized by an emulsion polymerization method, so that a special core-shell structure can be obtained, and the film-forming polymer has a damping characteristic of a wide temperature range.

The film-forming polymer has a high loss factor and a proper elastic modulus in a certain temperature range. Preferably having a dissipation factor of 0.4 or more in the temperature range of 10-30 c, more preferably having a dissipation factor of 0.4 or more in the temperature range of 5-35 c. The loss factor, also called loss factor, damping factor or loss tangent, is the ratio of the energy dissipated per cycle to the maximum stored energy in a cycle, and is an important parameter for measuring the damping characteristics of the system and determining the vibration energy dissipation capability thereof. The loss factor of the film-forming polymer or foam can be characterized by dynamic thermomechanical analysis (DMA) through a test method that sweeps the temperature at a constant frequency. The modulus of elasticity of the film-forming polymer is 0.5 to 20MPa, preferably 1 to 10MPa, more preferably 2 to 5 MPa.

The cushion foam layer of the present invention comprises an expanded microsphere which is a thermoplastic hollow polymer microsphere consisting of a thermoplastic polymer shell and an enclosed liquid alkane gas, the hollow spheres increasing the gas pressure in the shell when heated and the thermoplastic shell softening, whereby the expanded microsphere volume increases significantly, but the expanded microsphere shell becomes rigid again when cooled, but the volume remains unchanged. The expanded microspheres may have an initial expansion temperature of 80-200 ℃ and the expanded microspheres may have a diameter after expansion of 5-200 microns, preferably 30-100 microns, more preferably 40-80 microns.

The solvent may be water or an organic solvent, but for the sake of more environmental protection and safety of the production process, the preferred solvent of the present invention is water.

In order to impart a certain electrical conductivity to the cushion cotton material, an electrically conductive filler may be added to the composition. The preferable conductive filler is one or more of carbon nano tube, conductive nickel powder, nickel-plated glass fiber and conductive carbon powder. The adding proportion of the conductive filler is 1-20% of the total weight of the conductive filler added in the damping foam layer, and is preferably 3-10%. The surface resistivity of the conductive damping foam is measured to be 1x10³-1x10⁹The volume resistance of the conductive damping foam is measured to be 0.01-1000 ohm per square.

The invention further discloses a process for preparing the damping foam, which comprises the following steps:

the foam material provided by the invention has a density of 0.3-1.0 g/cc, preferably 0.5-0.8 g/cc. The thickness of the foam is preferably 0.05 to 0.5mm, more preferably 0.07 to 0.4 mm.

Compared with the prior art and products, the closed-cell foam material for the AMOLED has excellent shock absorption and impact resistance and fully applicable compressibility. As shown in fig. 3, the ultra-thin foam material for AMOLED module damping provided by the invention is thinned after being compressed, and meanwhile, the closed cell structure 4 therein is also extruded, and the closed cell structure is compressed by the same amount together with the foam material when being compressed, and the closed cell structure itself can absorb a part of compression energy, so that the foam material has a better energy absorption effect compared with the open cell structure.

The invention provides the following examples

Example 1:

the ultra-thin foam assembly for AMOLED module shock absorption provided by the embodiment comprises an ultra-thin shock absorption foam layer 1 and a release film layer 2, wherein the ultra-thin shock absorption foam layer is bonded with the release film layer through a glue layer 3, and the thickness of the ultra-thin shock absorption foam layer is 0.05-0.5 mm. The preparation method comprises the following steps:

s1, preparation of acrylate copolymer seed emulsion:

adding 20 g of butadiene, 110 g of styrene, 6 g of sodium dodecyl sulfate and 100 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 80 ℃, and continuously stirring for reaction for 3 hours to obtain prepolymer emulsion A;

then weighing 70 g of n-butyl acrylate, 2 g of sodium dodecyl sulfate and 60 g of water, adding the weighed materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dripping the n-butyl acrylate pre-emulsion and an ammonium persulfate aqueous solution into a reaction kettle containing the prepolymer emulsion A, and reacting for 3 hours at 80 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl sulfate and 4 g of mixed emulsifier of nonylphenol polyoxyethylene ether into a three-neck flask, adding 50 g of styrene and 50 g of acrylonitrile monomer, and stirring for pre-emulsification to obtain styrene/acrylonitrile pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 20 g and the initiator ammonium persulfate with the mass of 0.05 g, reacting for 4 hours at the temperature of 80 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 600mPa.S, a solids content of 50% and a glass transition temperature of 6 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 1 g of expanded hollow polyacrylonitrile copolymer microsphere FN80SDE purchased from Japan Sonn Japan K.K., 98 g of the film-forming polymer emulsion prepared in step S2, 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF, adding into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample. Foam samples of 50 microns, 100 microns, 200 microns and 400 microns in thickness were obtained by setting different blade gaps.

4 thicknesses were made with the formulation of example 1 and tested separately:

and (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 35% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 6 ℃. After synthesis of the core-shell emulsion, if the compatibility of the monomers for synthesizing the shell and the core is good, only one glass transition temperature can be generally measured, and the glass transition temperature is between the glass transition temperature of the core and the glass transition temperature of the shell, and this example shows that the Tg is about 6 ℃.

Example 2:

the ultra-thin foam assembly for AMOLED module shock absorption provided by the embodiment comprises an ultra-thin shock absorption foam layer 1 and a release film layer 2, wherein the ultra-thin shock absorption foam layer is bonded with the release film layer through a glue layer 3, and the thickness of the ultra-thin shock absorption foam layer is 0.05-0.5 mm. The preparation method comprises the following steps:

s1 preparation of acrylate copolymer seed emulsion

Adding 20 g of butadiene, 110 g of styrene, 6 g of sodium dodecyl sulfate and 100 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 80 ℃, and continuously stirring for reaction for 3 hours to obtain prepolymer emulsion A;

then weighing 70 g of n-butyl acrylate, 2 g of sodium dodecyl sulfate and 60 g of water, adding the weighed materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dripping the n-butyl acrylate pre-emulsion and an ammonium persulfate aqueous solution into a reaction kettle containing the prepolymer emulsion A, and reacting for 3 hours at 80 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl sulfate and 4 g of mixed emulsifier of nonylphenol polyoxyethylene ether into a three-neck flask, adding 50 g of styrene and 50 g of acrylonitrile monomer, and stirring for pre-emulsification to obtain isobornyl acrylate pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 20 g and the initiator ammonium persulfate with the mass of 0.1 g, reacting for 4 hours at the temperature of 80 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 600mPa.S, a solids content of 50% and a glass transition temperature of 6 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 2 g of expanded hollow polyacrylonitrile copolymer microspheres FN80SDE purchased from Japan Sonn Japan K.K., 96 g of the film-forming polymer emulsion prepared in the step S2, adding 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 40% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 6 ℃.

Example 3:

the ultra-thin foam assembly for AMOLED module shock absorption provided by the embodiment comprises an ultra-thin shock absorption foam layer 1 and a release film layer 2, wherein the ultra-thin shock absorption foam layer is bonded with the release film layer through a glue layer 3, and the thickness of the ultra-thin shock absorption foam layer is 0.05-0.5 mm. The preparation method comprises the following steps:

s1 preparation of acrylate copolymer seed emulsion

Adding 40 g of butadiene, 80 g of acrylonitrile, 6 g of sodium dodecyl sulfate and 100 g of deionized water into a reaction kettle, heating to 40 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 80 ℃, and continuously stirring for reaction for 3 hours to obtain prepolymer emulsion A;

then weighing 80 g of n-butyl acrylate, 2 g of sodium dodecyl benzene sulfonate and 60 g of water, adding the weighed materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dropwise adding the n-butyl acrylate pre-emulsion and the ammonium persulfate aqueous solution into a reaction kettle containing the prepolymer emulsion A, and reacting for 4 hours at 70 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl benzene sulfonate and 4 g of nonylphenol polyoxyethylene ether mixed emulsifier into a three-neck flask, adding 100 g of isobornyl acrylate monomer, and stirring and pre-emulsifying to obtain isobornyl acrylate pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 60 g and the initiator ammonium persulfate with the mass of 0.2 g, reacting for 4 hours at the temperature of 70 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 630mpa.s, a solids content of 50%, and a glass transition temperature of 5.1 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 2 g of expanded hollow polyacrylonitrile copolymer microspheres FN80SDE purchased from Japan Sonn Japan K.K., 96 g of the film-forming polymer emulsion prepared in the step S2, adding 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 40% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 5.1 ℃.

Example 4:

the ultra-thin foam assembly for AMOLED module shock absorption provided by the embodiment comprises an ultra-thin shock absorption foam layer 1 and a release film layer 2, wherein the ultra-thin shock absorption foam layer is bonded with the release film layer through a glue layer 3, and the thickness of the ultra-thin shock absorption foam layer is 0.05-0.5 mm. The preparation method comprises the following steps:

s1 preparation of acrylate copolymer seed emulsion

Adding 90 g of methyl acrylate, 50 g of acrylonitrile, 6 g of sodium dodecyl benzene sulfonate and 100 g of deionized water into a reaction kettle, heating to 45 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 35 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 70 ℃, and continuously stirring for reacting for 4 hours to obtain prepolymer emulsion A;

then weighing 60 g of isooctyl acrylate, 2 g of sodium dodecyl benzene sulfonate and 60 g of water, adding the materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dropwise adding isooctyl acrylate pre-emulsion and an ammonium persulfate aqueous solution into a reaction kettle filled with prepolymer emulsion A, and reacting for 4 hours at 70 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl benzene sulfonate and 4 g of nonylphenol polyoxyethylene ether mixed emulsifier into a three-neck flask, adding 100 g of methyl methacrylate monomer, and stirring and pre-emulsifying to obtain methyl methacrylate pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 40 g and the initiator ammonium persulfate with the mass of 0.2 g, reacting for 5 hours at the temperature of 70 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 580mPa.S, a solids content of 50% and a glass transition temperature of 10 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 2 g of expanded hollow polyacrylonitrile copolymer microspheres FN80SDE purchased from Japan Sonn Japan K.K., 96 g of the film-forming polymer emulsion prepared in the step S2, adding 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 40% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 10 ℃.

Example 5:

the ultra-thin foam assembly for AMOLED module shock absorption provided by the embodiment comprises an ultra-thin shock absorption foam layer 1 and a release film layer 2, wherein the ultra-thin shock absorption foam layer is bonded with the release film layer through a glue layer 3, and the thickness of the ultra-thin shock absorption foam layer is 0.05-0.5 mm. The preparation method comprises the following steps:

s1 preparation of acrylate copolymer seed emulsion

Adding 80 g of methyl acrylate, 40 g of styrene, 6 g of sodium dodecyl sulfate and 100 g of deionized water into a reaction kettle, heating to 45 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 35 minutes, keeping the reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 70 ℃, and continuously stirring for reacting for 4 hours to obtain prepolymer emulsion A;

then weighing 80 g of n-butyl acrylate, 2 g of sodium dodecyl sulfate and 60 g of water, adding the weighed materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dripping the isooctyl acrylate pre-emulsion and an ammonium persulfate aqueous solution into a reaction kettle containing the prepolymer emulsion A, and reacting for 4 hours at 70 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl sulfate and 4 g of mixed emulsifier of nonylphenol polyoxyethylene ether into a three-neck flask, adding 50 g of styrene and 50 g of acrylonitrile monomer, and stirring for pre-emulsification to obtain methyl methacrylate pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 50 g and the initiator ammonium persulfate with the mass of 0.2 g, reacting for 5 hours at the temperature of 70 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 650mPa.S, a solids content of 50% and a glass transition temperature of 5.3 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 2 g of expanded hollow polyacrylonitrile copolymer microspheres FN80SDE purchased from Japan Sonn Japan K.K., 96 g of the film-forming polymer emulsion prepared in the step S2, adding 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 40% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 5.3 ℃.

Example 6:

s1 preparation of acrylate copolymer seed emulsion

Adding 20 g of butadiene, 110 g of styrene, 6 g of sodium dodecyl sulfate and 100 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 75 ℃, and continuously stirring for reaction for 3.5 hours to obtain prepolymer emulsion A;

then weighing 70 g of n-butyl acrylate, 2 g of sodium dodecyl sulfate and 60 g of water, adding the weighed materials into a glass flask, slowly stirring and pre-emulsifying for 20 minutes, weighing 0.1 g of initiator ammonium persulfate and 20 g of water, mixing, pouring the mixture into a dropping funnel, simultaneously dripping the n-butyl acrylate pre-emulsion and an ammonium persulfate aqueous solution into a reaction kettle containing the prepolymer emulsion A, and reacting for 3 hours at 80 ℃ to obtain emulsion B;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl sulfate and 4 g of mixed emulsifier of nonylphenol polyoxyethylene ether into a three-neck flask, adding 50 g of styrene and 50 g of acrylonitrile monomer, and stirring for pre-emulsification to obtain styrene/acrylonitrile pre-emulsion C; -

Then, taking the emulsion B with the mass of 200 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion C with the mass of 20 g and the initiator ammonium persulfate with the mass of 0.05 g, reacting for 4 hours at the temperature of 80 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 600mPa.S, a solids content of 50% and a glass transition temperature of 6 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 1 g of expanded hollow polyacrylonitrile copolymer microsphere FN80SDE purchased from Japan Song Ben corporation, 98 g of the film-forming polymer emulsion prepared in the step S2, 5g of conductive nickel powder purchased from United states Borter company, 0.5 g of color paste KA100 purchased from Clariant company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF, adding into a mixing container, and stirring with a stirring paddle at a low speed for 30 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In this embodiment, the total volume of the cell structure is 30% of the volume of the ultrathin foam layer, the pore diameter of the closed cell structure is 20-80 μm, and the glass transition temperature is 6 ℃.

Example 7:

s1 preparation of acrylate copolymer seed emulsion

Adding 68 g of n-butyl acrylate, 52 g of styrene, 6 g of sodium dodecyl benzene sulfonate and 100 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.12 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 70 ℃, and continuously stirring for reaction for 4 hours to obtain a prepolymer emulsion D with the solid content of 50%;

s2 preparation of film-forming polymer emulsion

Adding 100 g of deionized water, 4 g of sodium dodecyl benzene sulfonate and 4 g of nonylphenol polyoxyethylene ether mixed emulsifier into a three-neck flask, adding 100 g of isobornyl acrylate monomer, and stirring and pre-emulsifying to obtain isobornyl acrylate pre-emulsion E;

then taking the emulsion D with the mass of 240 g prepared in the step S1 as a seed emulsion, synchronously dropwise adding the emulsion E with the mass of 50 g and the initiator ammonium persulfate with the mass of 0.1 g, reacting for 4 hours at the temperature of 80 ℃, cooling and discharging to obtain a film-forming polymer emulsion;

the film-forming polymer emulsion was found to have a viscosity of 700mPa.S, a solids content of 50% and a glass transition temperature of 3 ℃ as measured by differential scanning calorimetry after the emulsion was dried.

S3, preparation of the damping foam material dispersion liquid:

weighing 1 g of expanded hollow polyacrylonitrile copolymer microsphere FN80SDE purchased from Japan Sonn Japan K.K., 98 g of the film-forming polymer emulsion prepared in step S2, 0.5 g of color paste KA100 purchased from Clayan company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF, adding into a mixing vessel, and stirring with a stirring paddle at a low speed for 15 minutes until a uniform dispersion liquid is formed for later use;

s4, preparing a foam material:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

In the embodiment, the total volume of the foam pore structure is 30% of the volume of the ultrathin foam layer, the pore diameter of the closed pore structure is 20-80 microns, and the glass transition temperature of the foam is 3 ℃.

Comparative example 1:

(1) synthesis of acrylic ester copolymer emulsion:

adding 45 g of n-butyl acrylate, 55g of styrene, 6 g of sodium dodecyl sulfate and 80 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.1 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 80 ℃, and continuously stirring and reacting for 3 hours to obtain the polyacrylate/styrene copolymer emulsion. The film-forming polymer emulsion has viscosity of about 600mPa.S, solid content of 50%, and glass transition temperature of about 4% measured by differential scanning calorimetry after the emulsion is dried.

(2) Preparing a damping foam material dispersion liquid:

1 g of expanded hollow polyacrylonitrile copolymer microspheres FN80SDE available from Japan Sony corporation, 98 g of the film-forming polymer emulsion prepared in step S2, 0.5 g of color paste KA100 available from Clay, Inc., 0.1 g of defoaming agent BYK023 available from BYK, Inc., and 1 g of wetting agent WE-3650 available from BASF were weighed into a mixing vessel and stirred at a low speed for 15 minutes with a stirring blade to form a uniform dispersion for later use.

(3) Preparing damping foam:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample. Foam samples having a thickness of 100 microns, 200 microns and 400 microns were obtained by setting different blade gaps.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

Comparative example 2:

(1) synthesis of acrylic ester copolymer emulsion:

adding 45 g of n-butyl acrylate, 55g of styrene, 6 g of sodium dodecyl sulfate and 80 g of deionized water into a reaction kettle, heating to 50 ℃ under the protection of nitrogen, continuously stirring and emulsifying for 30 minutes, keeping a reaction device under the protection of nitrogen, dissolving 0.1 g of ammonium persulfate in 20 g of deionized water, dropwise adding the solution into the reaction solution, heating to 80 ℃, and continuously stirring and reacting for 3 hours to obtain the polyacrylate/styrene copolymer emulsion. The film-forming polymer emulsion has viscosity of about 600mPa.S, solid content of 50%, and glass transition temperature of about 4% measured by differential scanning calorimetry after the emulsion is dried.

(2) Preparing a damping foam material dispersion liquid:

weighing 1 g of expanded hollow polyacrylonitrile copolymer microsphere FN80SDE purchased from Japan Song Ben corporation, 98 g of the film-forming polymer emulsion prepared in the step S2, 5g of conductive nickel powder purchased from United states Borter company, 0.5 g of color paste KA100 purchased from Clariant company, 0.1 g of defoaming agent BYK023 purchased from BYK company and 1 g of wetting agent WE-3650 purchased from BASF, adding into a mixing container, and stirring with a stirring paddle at a low speed for 30 minutes until a uniform dispersion liquid is formed for later use;

(3) preparing damping foam:

and uniformly stirring and mixing the prepared dispersion liquid, coating the dispersion liquid on a PET release film in a scraper coating mode, putting the PET release film coated with wet glue into a 90-DEG C oven, drying for 10 minutes, and taking out to obtain a foam release film composite sample.

And (3) removing the dried foam layer from the PET release film, and testing the thickness, the density, the tensile modulus and the compression test of the foam layer, the qualitative test of the falling ball impact performance and the impact force absorption test of the foam.

The test method comprises the following steps:

(1) thickness measurement

Sampling, and placing the sampled sample in a standard testing environment for at least 24 hours;

during measurement, a sample is placed between the upper head plane and the lower head plane of the measuring head of the thickness gauge, the foam layer faces upwards, the upper measuring head slowly falls down during testing, and finally the upper measuring head covers the surface of the foam layer, and the distance from the edge of the upper measuring head to the edge of the sample is not less than 5mm as long as possible. Within 1 second after lowering the upper measuring head, the reading of the thickness gauge micrometer is recorded, in mm, to the nearest 0.001 mm. 5 points were measured for each sample, and data were recorded and an average value was calculated, wherein the distance between any two points was not less than 50 mm.

(2) Density test

Sampling, and placing the sampled sample in a standard testing environment for at least 24 hours;

the sample is cut into 10cm x10 cm samples under the condition of room temperature, the weight of the monomer foam is measured to be m, and the thickness measurement method is similar to the measurement condition and is marked as h.

Density calculation formula: p is m/h 100

(3) Tensile modulus test

Sampling, cutting the product into 3-5 strips with the size of 10mm multiplied by 150mm, and placing the strips in a standard test environment for at least 24 hours;

clamping two ends of the sample on a clamp of a tensile machine respectively by using an lnstron tensile testing machine, stretching and testing the elastic modulus at the speed of 300mm/min, recording test data, and taking an average value

(4) Compression testing

Cutting a sample into strips with the size of 50mm multiplied by 200mm, placing the strips in a standard test environment for 2 hours, then superposing the samples layer by layer to prepare samples with the size of 25mm multiplied by 10mm, and placing the samples in the standard test environment for at least 24 hours after finishing the preparation;

and testing the sample by using a universal mechanical press, wherein the compression speed is 5mm/min, performing compression test on the sample, and taking a compression strength data value corresponding to 25% compression ratio.

(5) Impact force absorption test

The sample is first cut to 70mm x 70mm size and placed in a standard test environment for at least 24 hours

Using a foam falling ball impact energy testing machine, enabling 13.75g of steel balls to freely fall from a height of 30cm, recording the size of original impact force received by the bottom sensor when no foam exists as F0, recording the size of the original impact force received by the bottom sensor when the foam is padded as F1, and calculating the buffering and absorption performance of a test sample: a% ([ (FO-F1)/F0 ]. times.100%

(6) Falling ball impact test

Firstly, cutting a sample into strips with the size of 100mm multiplied by 100mm, and placing the strips in a standard test environment for at least 24 hours;

mobile phone cover glass, sample specification: 60mm x 120mm x 0.7mm, and is applied to a sample of foam cotton material

The stainless steel ball with the weight of 55g and the diameter of 25mm is used for carrying out impact test on the mobile phone glass cover plate attached with the foam at the height of 500mm to see whether a sample is intact

(7) Dynamic thermomechanical analysis (DMA) testing

The instrument model is as follows: DMA/SDTA8610e for Mettler-Torido

And (3) taking off the foam sample from the release film, then carrying out DMA test, using a shearing mode, putting the sample into a small hole, starting an instrument, and carrying out test at the use frequency of 1Hz, the heating rate of 2 ℃/min and the temperature scanning from-40 ℃ to 60 ℃.

The data are collected and analyzed to obtain the storage modulus and loss modulus data of the foam at different temperatures, and the loss factors of the foam at different temperatures can be calculated.

Fig. 1, fig. 2 and fig. 3 are only some examples for illustrating the present invention, and do not represent all application scenarios of the present invention.

And (3) testing results:

from the test results, compared with the comparative examples, the foam samples of examples 1 to 4 have good impact resistance, and the foam samples of the same formula and different thicknesses have positive correlation on the absorption of impact force due to the higher damping loss performance of the film-forming polymer with the core-shell structure. In addition, about 2 percent of microsphere addition can endow the foam with better compression performance.

It should be understood that the above examples are only for clarity of illustration and are not intended to limit the embodiments. Other variations and modifications will be apparent to persons skilled in the art in light of the above description. And are neither required nor exhaustive of all embodiments. And obvious variations or modifications therefrom are within the scope of the invention.