Polyimide composite, a method of preparing thereof, and application thereof

Abstract

A polyimide composite, a method of preparing thereof, and an application thereof are provided. A general structure of the polyimide composite is: SiO.sub.2-(β-CD-Ada).sub.x/PI, and x is 3 to 5. The polyimide composite has the functions of self-repairing and anti-aging.

Claims

1. A polyimide composite, comprising: a polyimide resin and an assembly body distributed in the polyimide resin, wherein the polyimide resin is a polycondensate of an aromatic diamine and an aromatic dianhydride; the assembly body is made of β-cyclodextrin grafted SiO.sub.2 and reacted with adamantane by an inclusion reaction; and the polyimide composite has a structural formula as follows: SiO.sub.2-(β-CD-Ada).sub.x/PI, wherein x is 3 to 5.

2. A method of preparing the polyimide composite according to claim 1, comprising the following steps: (1) performing a graft reaction between SiO.sub.2 and β-cyclodextrin, wherein a product is SiO.sub.2-(β-CD).sub.x, and x is 3 to 5; (2) performing an inclusion reaction between the SiO.sub.2-(β-CD).sub.x and adamantane, wherein a product is SiO.sub.2-(β-CD-Ada).sub.x, and x is 3 to 5; (3) performing a polycondensation reaction, wherein diamine compound, dianhydride compound, and sodium amantadine are reacted through the polycondensation reaction, and a product is PAA; and (4) performing a grafting reaction and a cyclization reaction, wherein the PAA and the SiO.sub.2-(β-CD-Ada).sub.x are reacted through the grafting reaction and the cyclization reaction in order to form the polyimide composite, and the polyimide composite is SiO.sub.2-(β-CD-Ada).sub.x/PI, and x is 3 to 5.

3. The method of preparing the polyimide composite according to claim 2, wherein the β-cyclodextrin is fully dissolved in a NaOH solution in the step (1), then epichlorohydrin is added, and nano-sized SiO.sub.2 is slowly added at a stirring speed of 500 to 800 rpm, a grafting reaction is performed at 60° C., the grafting reaction is finished when viscosity occurs, then the solvent is removed by suspension distillation, a obtained dry solid is SiO.sub.2-(β-CD).sub.x, and a molar ratio of SiO.sub.2 to β-cyclodextrin is (0.25-5.0):1.

4. The method of preparing the polyimide composite according to claim 2, wherein the SiO.sub.2-(β-CD).sub.x and the adamantane are mixed in a molar ratio of (2-5):(1-3) in the step (2), and stirred for 24 to 96 hours under normal temperature conditions.

5. The method of preparing the polyimide composite according to claim 2, wherein a structural formula of the diamine compound in the step (3) is NH.sub.2—Ar—NH.sub.2, and the Ar is selected from one of ##STR00012##

6. The method of preparing the polyimide composite according to claim 2, wherein a structural formula of the dianhydride compound in the step (3) is ##STR00013##

7. The method of preparing the polyimide composite according to claim 2, wherein the diamine compound, the dianhydride compound and the sodium adamantane are mixed in a molar ratio of (1.05-2): 1: (1.1-9.9) and dissolved in a solvent at 80° C. for 6 to 10 hours in the step (3), and the solvent is one of N-methylpyrrolidone, N, N-dimethylformamide, and toluene.

8. The method of preparing the polyimide composite according to claim 2, wherein the PAA and the SiO.sub.2-(β-CD-Ada).sub.xare mixed in a mass ratio of (5-15):(85-95) in the step (4) and stirred at 0° C. for 24 to 96 hours, and then temperature is raised to 80° C. and a reaction is performed for 5 to 18 hours; and wherein the cyclization reaction in the step (4) comprises coating a graft reaction product on a glass substrate, baking and removing a solvent at 120° C., and then stepwise heating to 450° C., and then baking at a constant temperature for 0.8 to 1.2 hours to obtain the polyimide composite.

9. The method of preparing the polyimide composite according to claim 8, wherein a rate of stepwise heating is 4-8° C./min.

10. A method of forming a self-preparing coating, comprising coating the polyimide composite according to claim 1 on a surface of base material for coating.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a schematic view of a polyimide composite.

(2) FIG. 2 is a schematic view of anti-aging performance test for the polyimide composite.

(3) FIG. 3 is a schematic view of comparison of materials before and after undergoing micro-repair.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

(4) A polyimide composite includes a polyimide resin and an assembly body distributed in the polyimide resin, and the polyimide resin is a polycondensate of an aromatic diamine and an aromatic dianhydride; the assembly body is made of SiO.sub.2 grafted β-cyclodextrin and reacted with adamantane by an inclusion reaction; and the polyimide composite has a structural formula as follows: SiO.sub.2-(β-CD-Ada).sub.x/PI, and x is 3 to 5. The polyimide resin and the assembly body are connected by chemical bonds to form a stable compound. By introducing SiO.sub.2 as anti-aging nano-filled particles, it may impart reversible repair performance to weak bonds of materials. The re-formation of the bond is based on the good inclusion capacity of cyclodextrin and adamantane. When it is damaged, it makes the inclusion of cyclodextrin and adamantane again under a normal condition, so the material has an intelligent property such as self-repairing.

(5) A method of preparing the polyimide composite includes following steps: (1) performing a graft reaction between SiO.sub.2 and β-cyclodextrin, wherein a product is SiO.sub.2-(β-CD).sub.x, and x is 3 to 5; (2) performing an inclusion reaction between the SiO.sub.2-(β-CD).sub.x and adamantane, wherein a product is SiO.sub.2-(β-CD-Ada).sub.x, and x is 3 to 5; (3) performing a polycondensation reaction, wherein diamine compound, dianhydride compound, and sodium amantadine are reacted through the polycondensation reaction, and a product is PAA; and (4) performing a grafting reaction and a cyclization reaction, wherein the PAA and the SiO.sub.2-(β-CD-Ada).sub.x are reacted through the grafting reaction and the cyclization reaction in order to form the polyimide composite, and the polyimide composite is SiO.sub.2-(β-CD-Ada).sub.x/PI, and x is 3 to 5.

(6) Cyclodextrin is a cyclic oligosaccharide, and β-cyclodextrin is abbreviated as β-CD. In the step (1), based on the characteristics of insufficient surface atom coordination number, high surface energy, and easy agglomeration of SiO.sub.2, chemical reaction between the reaction groups on the surface of SiO.sub.2 and β-cyclodextrin is occurred to achieve surface grafting.

(7) β-cyclodextrin has a cavity structure and is driven by driving forces such as van der Waals force, hydrophobic force, and hydrogen bonding, and thus the β-cyclodextrin grafted with SiO.sub.2 may undergo an inclusion reaction with adamantane to form a stable inclusion compound SiO.sub.2-(β-CD-Ada).sub.x.

(8) The SiO.sub.2-(β-CD-Ada).sub.x and the PAA are reacted through a grafting reaction and a cyclization reaction in order to form a polyimide composite.

(9) Preferably, the β-cyclodextrin is fully dissolved in a NaOH solution in the step (1), then epichlorohydrin is added, and nano-sized SiO.sub.2 is slowly added at a stirring speed of 500 to 800 rpm, a grafting reaction is performed at 60° C., the grafting reaction is finished when viscosity occurs, then the solvent is removed by suspension distillation, a obtained dry solid is SiO.sub.2-(β-CD).sub.x, and a molar ratio of SiO.sub.2 to β-cyclodextrin is (0.25-5.0):1.

(10) Preferably, the SiO.sub.2-(β-CD).sub.x and the adamantane are mixed in a molar ratio of (2-5):(1-3) in the step (2), and stirred for 24 to 96 hours under normal temperature conditions.

(11) Preferably, a structural formula of the diamine compound in the step (3) is NH.sub.2-Ar-NH.sub.2, and the Ar is selected from one of

(12) ##STR00003##

(13) Preferably, a structural formula of the dianhydride compound in the step (3) is

(14) ##STR00004##

(15) Specifically, the diamine compound, the dianhydride compound and the sodium adamantane are mixed in a molar ratio of (1.05-2): 1: (1.1-9.9) and dissolved in a solvent at 80° C. for 6 to 10 hours in the step (3), and the solvent is one of N-methylpyrrolidone, N, N-dimethylformamide, and toluene.

(16) Specifically, the PAA and the SiO.sub.2-(β-CD-Ada).sub.x are mixed in a mass ratio of (5-15):(85-95) in the step (4) and stirred at 0° C. for 24 to 96 hours, and then temperature is raised to 80° C. and a reaction is performed for 5 to 18 hours.

(17) The cyclization reaction in the step (4) comprises coating a graft reaction product on a glass substrate, baking and removing a solvent at 120° C., and then stepwise heating to 450° C., and then baking at a constant temperature for 0.8 to 1.2 hours to obtain the polyimide composite.

(18) Preferably, a rate of stepwise heating is 4-8° C./min.

(19) Because the above polyimide composite or the polyimide composite prepared by the method described above has a self-repairing function and may have an ability to resist a certain external damage, it has excellent application properties for coatings or protective materials. The polyimide composite may be used alone or mixed with other ingredients so as to decorate and protect buildings.

(20) In the following, the present invention is further explained by way of Examples 1 to 3.

Example 1: Preparation of a Polyimide Composite

(21) (1) first, dissolving 10.0 g β-CD (0.88 mmol) in 16 mL NaOH (33 wt %) solution and sonicate for 30 min until the dissolution is completed. After cooling the solution to 30° C., add 6.89 mL epichlorohydrin is added quickly. In rapid stirring (600 rpm), slowly adding 0.89 g of nano-sized SiO.sub.2. After adding nano-sized SiO.sub.2 is completed, slowly raising the temperature to 60° C. and continue stirring for 25 hours to make the mixed solution appear relatively viscous. Then, the reaction is finished. Next, the solvent is removed by suspension distillation to obtain a dry solid, which is SiO.sub.2-(β-CD).sub.x; (2) mixing the SiO.sub.2 grafted β-cyclodextrin obtained in step (1) with 0.72 g adamantane, and stirring for 60 hours under normal temperature conditions to obtain an assembly body; (3) dissolving 1.4 g diamine compound, 2.3 g dianhydride compound and 0.70 g sodium adamantane in 30 mL N-methylpyrrolidone, and then reacting at 80° C. for 8 hours to obtain a polyamic acid solution named as PAA; (4) mixing 11 g PAA and 17 g assembly body, and the reaction is stirred at 0° C. for 60 hours, and then the temperature is raised to 80° C. Then, the obtained reaction product is spin-coated on a glass substrate, and 70% the solvent is baked at 120° C. The temperature is raised to 450° C. in steps at a rate of 6° C./min, and then is baked for 1 hour at a constant temperature to obtain a polyimide composite. The schematic view of polyimide composite structure is shown in FIG. 1.

(22) The structural formula of the diamine compound is

(23) ##STR00005##
The structural formula of the dianhydride compound is

(24) ##STR00006##

Example 2: Preparation of a Polyimide Composite

(25) The preparation method of Example 1 is adopted, except that the structural formula of the diamine compound is

(26) ##STR00007##
The amount of diamine compound is 1.5 g.

Example 3: Preparation of a Polyimide Composite

(27) The preparation method of Example 1 is adopted, except that the structural formula of the diamine compound is

(28) ##STR00008##
The amount of diamine compound is 1.05 g.

Example 4: Preparation of a Polyimide Composite

(29) The preparation method of Example 1 is adopted, except that the structural formula of the diamine compound is

(30) ##STR00009##
The amount of diamine compound is 1.6 g.

Example 5: Preparation of a Polyimide Composite

(31) The preparation method of Example 1 is adopted, except that the structural formula of the diamine compound is

(32) ##STR00010##
The amount of diamine compound is 0.95 g.

Example 6: Preparation of a Polyimide Composite

(33) The preparation method of Example 2 is adopted, except that the structural formula of the dianhydride compound is

(34) ##STR00011##
The amount of dianhydride compound is 2.8 g.

(35) Performance Test:

(36) 1. Anti-Aging Performance Test:

(37) Taking two metal plates with polytetrafluoroethylene (PTFE) as base material. The thickness, size, and material of the plates are exactly the same. A surface of one of the metal plates is coated with the polyimide composite prepared in Example 1. The thickness of the coating is 0.1 mm. After coating, the color of the metal plate is light green as shown in FIG. 2 (a). A surface of another metal plate is painted with 0.1 mm Teflon. After coating, the color of the plate is white as shown in FIG. 2(d).

(38) Two metal plates are subjected to a strong ultraviolet accelerated aging test. After the metal plates coated with the polyimide composite are subjected to a strong ultraviolet accelerated aging test, the color of the plate is shown in FIG. 2 (b). It almost no change as light green color of FIG. 2 (a). However, after the metal plate coated with polytetrafluoroethylene is subjected to the accelerated ultraviolet aging test, the color of the plate body is shown in FIG. 2 (c), which shows a tan that is greatly different from the color shown in FIG. 2 (d). Therefore, it can be seen that the material prepared by the present invention has obvious anti-aging properties.

(39) 2. Self-Repairing Performance Test

(40) Experimental process: use a scalpel to draw a scratch of the obtained SiO.sub.2-(β-CD-Ada).sub.x/PI composite film about 10 mm, and observe the cross-section and contour of the scratch with a laser confocal. Set 12 h to 24 h, observe the microscopic view of the cracks again and compare them. As a result, a laser confocal scanning microscope is used to study the micro-repair performance of the material, and the results are shown in FIG. 3. It can be seen from FIG. 3 that the scratches are basically disappear after repairing, that is, the material prepared by the present invention may achieve the self-repairing function.

INDUSTRIAL APPLICABILITY

(41) The subject matter of this application can be manufactured and used in industry with industrial applicability.