Polymer film, method of preparing the same, and flexible folding panel

Abstract

The present disclosure provides a polymer film, a method of preparing the same, and a flexible folded panel. The polymer film includes a substrate and a strengthening layer, wherein the strengthening layer includes a polymer, side chains of the polymer include a plurality of rigid segments and a plurality of flexible segments, which modify and strengthen the side chains of the polymer. The monomer of the polymer is subjected to a series of reactions, to synthesize the polymer, and the polymer film enhance hardness of a cover plate of a panel and improve the anti-friction properties and bendability.

Claims

1. A method of preparing a polymer film, comprising the following steps: S100: mixing bis(3-bromo-4-isocyanatophenyl)methane with an additive for reaction to prepare a monomer; S101: reacting the monomer with oxalic acid to prepare a polymer; and S102: coating the polymer on a substrate to form the polymer film, wherein the monomer comprises: N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(4-hexylnaphthalen-1-amine) or N,N′-(methylene bis(6-isocyanato-3,1-phenylene)) bis(10-octylanthracene-9-amine); and the polymer has a chemical structural formula as follows: ##STR00010## wherein n is a positive integer.

2. The method of preparing the polymer film according to claim 1, wherein the additive comprises 4-hexylnaphthylamine.

3. The method of preparing the polymer film according to claim 1, wherein the step S100 further comprises the following steps: S200: adding the bis(3-bromo-4-isocyanatophenyl)methane and 4-hexylnaphthylamine to a flask, and adding cesium carbonate, cuprous iodide and 18-crown-6 to the flask; S201: introducing argon gas into the flask, and adding deoxygenated N,N′-dimethylpropylene urea to the flask to form a mixture, and reacting the mixture at 180° C. for 24 hours; and S202: cooling the flask to room temperature, adding ice water to the flask, followed by extraction three times with dichloromethane, then combining organic extracts, after that, adding silica gel to the organic extracts, removing solvent from the organic extracts, and carrying out column chromatography to obtain the monomer.

4. The method of preparing the polymer film according to claim 3, wherein the step S101 further comprises the following steps: S300: mixing the N,N′-(methylenebis(6-isocyanato-3,1-phenylene)) bis(4-hexylnaphthalen-1-amine) and the oxalic acid in the flask for reaction at 80° C. for 12 hours; S301: precipitating the mixture with methanol to obtain a white solid, and then extracting the white solid in n-hexane and acetone for two days to obtain the polymer.

5. The method of preparing the polymer film according to claim 4, wherein the step S300 comprises: introducing argon gas into the flask and adding diluted hydrochloric acid to the flask.

6. The method of preparing the polymer film according to claim 1, wherein the additive comprises 10-amino-9-octylanthracene.

7. The method of preparing the polymer film according to claim 1, wherein the step S100 further comprises the following steps: S400: adding the bis(3-bromo-4-isocyanatophenyl)methane and 10-amino-9-octylanthracene to a flask; S401: introducing argon gas into the flask, and adding deoxygenated N,N′-dimethylpropylene urea to the flask to form a mixture, and reacting the mixture at 180° C. for 24 hours; and S402: cooling the flask to room temperature, adding ice water to the flask, followed by extraction three times with dichloromethane, then combining organic extracts, after that, adding silica gel to the flask, removing solvent from the organic extracts, and carrying out column chromatography to obtain the monomer.

8. The method of preparing the polymer film according to claim 7, wherein the step S400 further comprises: adding cerium carbonate, cuprous iodide and 18-crown-6 to the flask.

9. The method of preparing the polymer film according to claim 3, wherein the step S101 further comprises the following steps: S500: mixing the N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(10-octylanthracene-9-amine) and the oxalic acid in a flask, and introducing argon gas and diluted hydrochloric acid for a reaction at 80° C. for 12 hours to obtain a mixture; and S501: precipitating the mixture with methanol to obtain a white solid, and then extracting the white solid in n-hexane and acetone for two days to obtain the polymer.

10. A polymer film comprising: a substrate; and a strengthening layer; wherein the strengthening layer is disposed on the substrate, the strengthening layer comprises a polymer, and side chains of the polymer comprise a plurality of rigid segments and a plurality of flexible segments, wherein the polymer has a chemical structural formula as follows: ##STR00011## wherein n is a positive integer.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a schematic structural diagram of a polymer film according to an embodiment of the present disclosure.

(2) FIG. 2 is a flow chart showing a process for preparing a polymer film according to an embodiment of the present disclosure.

(3) FIG. 3 is a schematic structural diagram of a flexible folding panel according to an embodiment of the present disclosure.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

(4) The following description of various embodiments refers to the additional drawings, to illustrate the specific embodiments of the present disclosure.

(5) In order to prevent cracking of the display screen, especially the cracking of the flexible folding screen, it is generally necessary to add a cover plate to the screen, which thereby provides a good protection for the screen. However, in practical applications, especially on some flexible folding screens, the hardness of the cover plate and its bending recovery performance cannot be balanced with each other, and there are problems such as excessive or insufficient hardness and poor bendability.

(6) In an embodiment of the present disclosure, a polymer film is provided. A cover plate for protection is mainly composed of a hardened layer and a flexible substrate, and the polymer film provided by the present disclosure is coated on the hardened layer, thereby adjusting the surface hardness and bendability of the entire cover plate. As shown in FIG. 1, FIG. 1 is a schematic structural diagram of a polymer film according to an embodiment of the present disclosure. The polymer film includes a substrate 100 and a strengthening layer 101. The strengthening layer 101 is disposed on the substrate 100, wherein the strengthening layer 101 further includes a polymer, and the strengthening layer 101 is composed of the polymers.

(7) Specifically, the polymer is Polymer A having a chemical structural formula as follows:

(8) ##STR00004##
wherein n is a positive integer.

(9) Specifically, the polymer is Polymer B having a chemical structural formula as follows:

(10) ##STR00005##
wherein n is a positive integer.

(11) Side chains of the polymer include a plurality of rigid segments and a plurality of flexible segments to modify the side chains of the polymer, thereby achieving a purpose of reinforcement. The polymer provided by the embodiments of the present disclosure strengthens a film by introducing different proportions of rigid segments and flexible segments on the side chains and adjusting a ratio therebetween to meet the requirements of the flexible foldable display.

(12) An embodiment of the present disclosure provides a method of preparing a polymer film. As shown in FIG. 2, FIG. 2 is a flow chart showing the method of preparing the polymer film according to an embodiment of the present disclosure, which includes the following steps:

(13) S100: mixing bis(3-bromo-4-isocyanatophenyl)methane with an additive for reaction to prepare a monomer.

(14) In step S100, a monomer of the polymer is mainly prepared for the preparation of the polymer in the subsequent processes.

(15) S101: reacting the monomer with oxalic acid to prepare a polymer.

(16) The monomer is obtained in the step S100 and subjected to a series of chemical synthesis reactions to obtain the polymer of this embodiment of the present disclosure finally.

(17) S102: coating the polymer on a substrate to form the polymer film

(18) Finally, the prepared polymer is coated on a substrate and dried to form a film serving as a strengthening layer on a cover plate.

(19) Specifically, in the process of preparing the polymer, the monomer of the polymer includes: N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(4-hexylnaphthalen-1-amine) or N,N′-(methylene bis(6-isocyanato-3,1-phenylene)) bis(10-octylanthracene-9-amine).

(20) When the polymer is Polymer A, a chemical formula of the monomer of Polymer A is C.sub.47H.sub.48N.sub.4O.sub.2, that is, N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(4-hexylnaphthalen-1-amine).

(21) Polymer A is synthesized from monomers of Polymer A through a series of reactions. Specifically, the monomers of Polymer A are first synthesized, and the synthesis process is as follows:

(22) Bis(3-bromo-4-isocyanatophenyl)methane (4.08 g, 10 mmol) and 4-hexylnaphthylamine (4.54 g, 20 mmol) were added to a 100 ml two-necked flask.

(23) Then, additives which include cesium carbonate (4.62 g, 24 mmol), cuprous iodide (228 mg, 1.2 mmol) and 18-crown-6 (104 mg, 0.4 mmol) were added to the flask.

(24) After the addition was completed, elution was carried out three times, argon gas was introduced into the flask while 50 mL of deoxygenated N,N-dimethylpropylene urea (DMPU) was added to the flask, and then the mixture was placed at 180° C. for reaction for 24 hours.

(25) Finally, the flask was cooled to room temperature, and the mixture was poured into 100 ml of ice water, followed by extraction three times with dichloromethane, and the organic extracts were combined, after that, silica gel was added to the organic extracts, and solvent was removed from the organic extracts. Then, a separation was carried out by column chromatography, wherein the separation liquid was dichloromethane and n-hexane in a volume ratio of 1:1, a white solid of 4.2 g was obtained, and a yield of the white solid was 60% throughout the preparation process, which is higher than that in the existing production process.

(26) Specifically, a synthetic chemical reaction of the monomer is as follows:

(27) ##STR00006##

(28) The above-mentioned white solid substance was subjected to nuclear magnetic detection and found to match the chemical formula of the monomer of the polymer A.

(29) After the preparation of the monomer of the polymer A is completed, the polymer A is prepared from the monomer. Specifically, the following steps are included:

(30) First, the monomer of Polymer A, namely N,N′-(methylenebis(6-isocyanato-3,1-phenylene)) bis(4-hexylnaphthalen-1-amine) (4.2 g, 6 mmol) and the oxalic acid (0.558 g, 6.2 mmol) were added to a 25 ml round bottom flask.

(31) Then, argon gas was introduced and oxygen was purged out, and 10 ml of diluted hydrochloric acid was added, the mixture was reacted at 80° C. for 12 hours, and then the reaction was stopped.

(32) Finally, the mixture was precipitated with 50 ml of methanol to give a white solid, and the white solid was eluted sequentially in n-hexane and acetone for two days to give 2.51 g of a colorless solid.

(33) The yield of the polymer was determined to be 53% in the synthesis process. The polymer had a weight average molecular of 2,356 kg/mol, a number average molecular weight of 1980 kg/mol, and a dispersion of 1.83.

(34) Specifically, the synthetic reaction from the monomer to the polymer is as follows:

(35) ##STR00007##

(36) Preferably, when the polymer is Polymer B, during the synthesis, Polymer B is prepared from a monomer of Polymer B through a series of chemical synthesis. Specifically, the chemical formula of the monomer of Polymer B is C.sub.59H.sub.60N.sub.4O.sub.2, that is, N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(10-octylanthracene-9-amine).

(37) Polymer B is synthesized from monomers of Polymer B through a series of reactions. Specifically, the monomers of Polymer B are first synthesized, and the synthesis process is as follows:

(38) First, bis(3-bromo-4-isocyanatophenyl)methane (4.08 g, 10 mmol) and 10-amino-9-octylanthracene (6.1 g, 20 mmol) were added to a 100 ml two-necked flask.

(39) Then, additives which include cesium carbonate (4.62 g, 24 mmol), cuprous iodide (228 mg, 1.2 mmol) and 18-crown-6 (104 mg, 0.4 mmol) were added to the flask.

(40) Subsequently, elution was carried out three times, argon gas was introduced into the flask while 50 mL of deoxygenated N,N-dimethylpropylene urea (DMPU) was added to the flask, and then the mixture was placed at 180° C. for reaction for 24 hours.

(41) Finally, the flask was cooled to room temperature, and the mixture was poured into 100 ml of ice water, followed by extraction three times with dichloromethane, and the organic extracts were combined, after that, silica gel was added to the organic extracts, and solvent was removed from the organic extracts. Then, a separation was carried out by column chromatography (dichloromethane: n-hexane v/v=1:2) to obtain 4.1 g of a white solid with a yield of 48%.

(42) Specifically, a synthetic chemical reaction of the monomer is as follows:

(43) ##STR00008##

(44) The above-mentioned white solid substance was subjected to nuclear magnetic detection and found to match the chemical formula of the monomer of Polymer B.

(45) After the preparation of the monomer of Polymer B is completed, Polymer B is prepared from the monomer. Specifically, the following steps are included:

(46) First, N,N′-(methylenebis(6-isocyanato-3,1-phenylene))bis(10-octylanthracene-9-amine) (4.1 g, 4.7 mmol) and oxalic acid (0.441 g, 4.9 mmol) were added to a 25 ml round bottom flask.

(47) Subsequently, argon gas was introduced and oxygen was purged out, and 10 ml of diluted hydrochloric acid was added, the mixture was reacted at 80° C. for 12 hours, and then the reaction was stopped.

(48) Finally, the mixture was precipitated with 50 ml of methanol to give a white solid, and the white solid was eluted sequentially in n-hexane and acetone for two days to give a colorless solid.

(49) The obtained white solid had a mass of 3.07 g and a yield of 68%. Polymer B had a weight average molecular weight of 2578 kg/mol, a number average molecular weight of 2043 kg/mol, and a dispersion of 1.79.

(50) Specifically, the synthetic reaction from the monomer to Polymer B is as follows:

(51) ##STR00009##

(52) Finally, the polymer film provided by the embodiments of the present disclosure was prepared, which is applied to the cover plate, and when Polymer A was used as the strengthening layer coated on transparent polyimide, the cover plate having a surface hardness of 2H was obtained; and when Polymer B was used as the strengthening layer coated on transparent polyimide, the cover plate having a surface hardness of 3H was obtained. As such, the hardness of the hardened layer is improved, and also good bendability and anti-friction properties are provided.

(53) An embodiment of the present disclosure further provides a flexible folding panel. As shown in FIG. 3, FIG. 3 is a flexible folding panel according to an embodiment of the present disclosure. The flexible folding panel 300 is provided with a polymer film 301 according to an embodiment of the present disclosure, and the polymer film 301 is prepared by the preparation method according to an embodiment of the present disclosure.

(54) The polymer film, the method of preparing the same, and the flexible folding panel provided by the embodiments of the present disclosure are described in detail above. The description of the above embodiments is only for helping to understand the technical solutions of the present disclosure and the core ideas thereof; It should be understood by those skilled in the art that the technical solutions described in the foregoing embodiments may be modified, and the modifications or substitutions do not depart from the scope of the technical solutions of the embodiments of the present disclosure.