A boron nitride nanosheet-aromatic fiber nanofiber composite film and a preparation method thereof

Abstract

The application belongs to the technical field of composite film materials, and particularly relates to a boron nitride nanosheet-aramid nanofiber composite film and a preparation method thereof. 2+ / SA crosslinking solution; hexagonal boron nitride is added into the Ca 2+ / SA crosslinking solution, and pre-infiltration is realized through magnetic stirring to obtain a pre-infiltrated SA / BNNS solution; the pre-infiltrated SA / BNNS solution is subjected to ball milling and washing to obtain a BNNS / water suspension; the BNNS / water suspension is mixed with an ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution; the BNNS / ANF mixed solution is subjected to vacuum filtration, drying and hot-pressing treatment to obtain the boron nitride nanosheet-aramid nanofiber composite film; and the application improves the interfacial phonon scattering between BNNS, so that the interfacial density of the material is lower and the contact area of the interface is larger, thereby improving the thermal conductivity of the composite film.

Description

Technical Field

[0001] The present invention belongs to the technical field of composite film materials, and in particular relates to a boron nitride nanosheet-aramid nanofiber composite film and a preparation method thereof. Background Art

[0002] In recent years, with the rapid development of microelectronics technology and integrated circuits, electronic devices are increasingly tending towards high integration, high power, and multifunctionality. However, this has led to a serious heating problem in electronic devices. On the one hand, the extensive use of integrated circuits and microelectronic components has reduced the size of devices by thousands of times, greatly improving their portability and popularity, but at the same time has also caused serious heat accumulation. On the other hand, the ever-increasing operating power has also greatly increased the heat generated during operation, resulting in increasingly high operating temperatures for electronic components. Heat accumulation in devices not only affects the stability and reliability of electronic components, but also causes a series of problems such as material aging and failure, thereby affecting the stable operation of the entire electronic device and shortening its operating life. Therefore, thermal management of electronic devices is a key factor in ensuring the normal operation of electronic devices, and the exploration of thermal management materials with excellent comprehensive performance is urgent.

[0003] Polymer-based high-thermal conductivity composite materials are currently one of the main research directions for improving thermal management efficiency, but how to maximize the intrinsic high thermal conductivity advantages of fillers requires further exploration. Hexagonal boron nitride (h-BN) is a graphene-like layered material with thick flakes and a smooth surface, making it difficult to stack tightly and having poor wettability and dispersibility with polymers. Therefore, h-BN is usually exfoliated into boron nitride nanosheets (BNNS) or functionalized with organic matter and then filled into polymers to construct thermally conductive composite materials. However, existing exfoliation methods make it difficult to prepare large, single-layer BNNS, which leads to low thermal conductivity of the material, which seriously affects the stability and reliability of electronic components. Summary of the Invention

[0004] In response to the technical problems existing in the prior art, the present invention provides a boron nitride nanosheet-aramid nanofiber composite film and a preparation method thereof, so as to solve the technical problem that the existing peeling method is difficult to prepare large and single-layer BNNS, which in turn leads to low thermal conductivity of the material.

[0005] In order to achieve the above object, the technical solution adopted by the present invention is:

[0006] The present invention provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising:

[0007] Calcium chloride is dissolved in sodium alginate aqueous solution to obtain Ca 2+ / SA cross-linking solution;

[0008] Adding hexagonal boron nitride to Ca 2+ / SA cross-linking solution, pre-infiltration is achieved by magnetic stirring to obtain a pre-infiltrated SA / BNNS solution; the pre-infiltrated SA / BNNS solution is ball milled and washed to obtain a BNNS / water suspension;

[0009] The BNNS / water suspension was mixed with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution;

[0010] The BNNS / ANF mixed solution was vacuum filtered, dried and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0011] Furthermore, Ca 2+ Ca / SA cross-linking solution 2+ The concentration is 1-4mmol / L.

[0012] Furthermore, the pre-soaked SA / BNNS solution was ball-milled and washed to obtain a BNNS / water suspension, and the ball-milling time was 12-24 h.

[0013] Furthermore, the pre-soaked SA / BNNS solution was ball-milled and washed to obtain a BNNS / water suspension, which was washed with deionized water.

[0014] Furthermore, the concentration of the BNNS / water suspension is 5-10 mg / mL.

[0015] Furthermore, the preparation process of ANF / DMSO dispersion is as follows:

[0016] Para-PPTA fibers and potassium hydroxide were dispersed in DMSO and stirred continuously to obtain an ANF / DMSO dispersion.

[0017] Furthermore, the concentration of the ANF / DMSO dispersion is 1-5 mg / mL.

[0018] Furthermore, the preparation process of the sodium alginate aqueous solution is specifically as follows:

[0019] Sodium alginate is added into deionized water, stirred and dissolved to obtain a sodium alginate aqueous solution.

[0020] The present invention also provides a boron nitride nanosheet-aramid nanofiber composite film, which is prepared by using the preparation method of the boron nitride nanosheet-aramid nanofiber composite film.

[0021] Furthermore, the thermal conductivity of the boron nitride nanosheet-aramid nanofiber composite film is 23.86-27.57 W·m-1 ·K -1 .

[0022] Compared with the prior art, the present invention has the following beneficial effects:

[0023] The present invention provides a boron nitride nanosheet-aramid nanofiber composite film and a preparation method thereof. The boron nitride nanosheet-aramid nanofiber composite film is prepared by vacuum filtration and hot pressing using ANF as a polymer substrate and BNNS as a thermally conductive filler. Calcium ion cross-linking of sodium alginate is assisted by ball milling exfoliation to obtain high-aspect-ratio BNNS with large lateral dimensions and small thickness, thereby improving interfacial phonon scattering between the BNNSs, lowering the interface density of the composite material and increasing the interface contact area, thereby improving the thermal conductivity of the composite film. Secondly, the ANF and BNNS are effectively compounded by hot pressing, and the BNNSs are oriented in-plane to construct a continuous in-plane thermal conductive network, so that the composite material has good thermal conductivity and can be applied in fields with high thermal conductivity requirements. BRIEF DESCRIPTION OF THE DRAWINGS

[0024] In order to more clearly illustrate the embodiments of the present application or the technical solutions in the prior art, the following briefly introduces the drawings required for use in the embodiments or the description of the prior art. Obviously, the drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without any creative work.

[0025] Figure 1 is the SEM image of BNNS after ball milling in the comparative example;

[0026] Figure 2 SEM image of BNNS after ball milling in Example 5

[0027] Figure 3 TEM image of BNNS after ball milling in Example 5;

[0028] Figure 4 Graphs showing the thermal conductivity of the boron nitride nanosheet-aramid nanofiber composite films prepared in Examples 3-5 and the comparative example. DETAILED DESCRIPTION

[0029] In order to make the technical problems, technical solutions, and beneficial effects solved by this application more clearly understood, the technical solutions in the embodiments of this application will be clearly and completely described below in conjunction with the accompanying drawings in the embodiments of this application; it is obvious that the described embodiments are only part of the embodiments of this application, not all of the embodiments. Based on the embodiments in this application, all other embodiments obtained by ordinary technicians in this field without making any creative efforts shall fall within the scope of protection of this application.

[0030] The present invention provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0031] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a SA aqueous solution with a concentration of 1-2 wt%.

[0032] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain Ca 2+ Ca concentration of 1-4 mmol / L 2+ / SA cross-linking solution.

[0033] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 40-60 mg / mL, and magnetic stirring is performed for 36-60 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0034] Step 4: Measure 10-30 mL of the pre-soaked SA / BNNS solution, ball-mill at 300-400 rpm for 12-24 h, then wash with deionized water 3-5 times, and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 5-10 mg / mL.

[0035] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 1-5 mg / mL.

[0036] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0037] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0038] Preparation principle:

[0039] The method for preparing the boron nitride nanosheet-aramid nanofiber composite film of the present invention comprises ball milling and exfoliating h-BN using an SA aqueous solution according to the viscosity, and further introducing Ca 2+The SA chains are cross-linked to enhance their interfacial interaction with h-BN, aiming to increase the lateral size and thin layer of the prepared BNNSs to a greater extent; ANF and BNNS are effectively compounded by hot pressing, and the BNNS are oriented in-plane to construct a continuous in-plane thermal conductive network, so that the composite material has good thermal conductivity; among them, ANF has excellent mechanical reinforcement properties, thermal stability, insulation and good processability, and is used as a mechanical reinforcement phase of the polymer matrix; the prepared BNNS with large lateral size and thin thickness has high intrinsic thermal conductivity, electrical insulation, chemical stability and thermal stability. The addition of BNNS can not only effectively enhance the thermal conductivity of the polymer matrix, but also significantly enhance the breakdown strength of the material, reduce dielectric loss, and obtain a polymer-based composite material with excellent insulation properties.

[0040] Example 1

[0041] This embodiment 1 provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0042] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a 1 wt% SA aqueous solution.

[0043] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain a CaCl2 solution with a concentration of 1 mmol / L. 2+ / SA cross-linking solution.

[0044] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 40 mg / mL, and magnetic stirring is performed for 36 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0045] Step 4: Measure 10 mL of the pre-soaked SA / BNNS solution, ball-mill at 300 rpm for 12 h, then wash three times with deionized water and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 5 mg / mL.

[0046] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 1 mg / mL.

[0047] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0048] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0049] Example 2

[0050] This embodiment 2 provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0051] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a 2 wt% SA aqueous solution.

[0052] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain a CaCl2 solution with a concentration of 4 mmol / L. 2+ / SA cross-linking solution.

[0053] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 60 mg / mL, and magnetic stirring is performed for 60 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0054] Step 4: Measure 30 mL of the pre-soaked SA / BNNS solution, ball-mill at 400 rpm for 24 h, then wash with deionized water five times and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 10 mg / mL.

[0055] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 5 mg / mL.

[0056] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0057] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0058] Example 3

[0059] This embodiment 3 provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0060] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a SA aqueous solution with a concentration of 1.5 wt%.

[0061] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain a CaCl2 solution with a concentration of 1 mmol / L. 2+ / SA cross-linking solution.

[0062] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 50 mg / mL, and magnetic stirring is performed for 48 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0063] Step 4: Measure 20 mL of the pre-soaked SA / BNNS solution, ball-mill at 350 rpm for 18 h, then wash four times with deionized water and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 7 mg / mL.

[0064] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 3 mg / mL.

[0065] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0066] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0067] Example 4

[0068] This embodiment 4 provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0069] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a SA aqueous solution with a concentration of 1.2 wt%.

[0070] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain a CaCl2 solution with a concentration of 2 mmol / L. 2+ / SA cross-linking solution.

[0071] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 50 mg / mL, and magnetic stirring is performed for 48 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0072] Step 4: Measure 10 mL of the pre-soaked SA / BNNS solution, ball-mill at 400 rpm for 24 h, then wash four times with deionized water and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 8 mg / mL.

[0073] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 4 mg / mL.

[0074] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0075] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0076] Example 5

[0077] This embodiment 5 provides a method for preparing a boron nitride nanosheet-aramid nanofiber composite film, comprising the following steps:

[0078] Step 1: Add sodium alginate (SA) into deionized water, stir and dissolve to obtain a 1 wt% SA aqueous solution.

[0079] Step 2: Dissolve calcium chloride (CaCl2) in SA aqueous solution to obtain a CaCl2 solution with a concentration of 4 mmol / L. 2+ / SA cross-linking solution.

[0080] Step 3: Add hexagonal boron nitride (h-BN) to Ca 2+ / SA solution to obtain a mixed solution; wherein the concentration of h-BN in the mixed solution is 50 mg / mL, and magnetic stirring is performed for 48 hours to achieve pre-infiltration to obtain a pre-infiltrated SA / BNNS solution.

[0081] Step 4: Measure 10 mL of the pre-soaked SA / BNNS solution, ball-mill at 400 rpm for 24 h, then wash four times with deionized water and dilute with deionized water to obtain a BNNS / water suspension; wherein the concentration of BNNS in the BNNS / water suspension is 7 mg / mL.

[0082] Step 5: Mix the para-PPTA fiber and KOH and disperse them in DMSO, stirring continuously to obtain an ANF / DMSO dispersion with a concentration of 2.5 mg / mL.

[0083] Step 6: Mix the BNNS / water suspension with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution.

[0084] Step 7: The BNNS / ANF mixed solution is vacuum filtered, dried, and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

[0085] Comparative Example

[0086] The process and principle of this comparative example are basically the same as those of the above-mentioned Example 5, except that:

[0087] The amount of calcium chloride added in step 2 of Example 5 was adjusted to 0, that is, no calcium chloride was added in this comparative example; the remaining steps were basically the same and will not be repeated here.

[0088] As attached Figure 1-2 As shown, attached Figure 1 The SEM images of the BNNS after ball milling in the comparative example are given in the appendix. Figure 2 The SEM images of the BNNS after ball milling in Example 5 are given in FIG. Figure 1-2 As can be seen, the introduction of Ca 2+ The lateral size of BNNSs was significantly increased after exfoliation, and the thickness of the finished product was thin, and the curling of the nanosheets could be observed. This is due to the fact that Ca 2+ The cross-linking degree of SA is promoted and the resistance of h-BN layer to impact force is enhanced.

[0089] As attached Figure 3 As shown, attached Figure 3 The TEM image of the BNNS after ball milling in Example 5 is given in FIG, which also shows that the BNNS prepared by exfoliation has the characteristics of large lateral size and thin thickness.

[0090] As attached Figure 4 As shown, attached Figure 4 The thermal conductivity diagrams of the boron nitride nanosheet-aramid nanofiber composite films prepared in Examples 3-5 and Comparative Examples are given in FIG. 2+ The highest TC value was 27.57 W·m when the concentration was 4 mmol / L. -1 ·K -1 , and the TC value increases with Ca 2+ The reason for the synchronous increase in concentration may be that the lateral size of BNNS increases, thereby reducing phonon scattering at the boundary; secondly, the microstructure of the resulting film after the composite of ANF and BNNS is denser and the interface interaction is stronger.

[0091] The boron nitride nanosheet-aramid nanofiber composite film and its preparation method described in the present invention use calcium ion cross-linked sodium alginate to assist ball milling exfoliation to prepare high-aspect ratio BNNS with large lateral dimensions and small thickness, thereby improving the interface phonon scattering between the BNNS, making the interface density of the composite material lower and the interface contact area larger, thereby improving the thermal conductivity of the composite film; secondly, the ANF and BNNS are effectively compounded by hot pressing, and the BNNS are oriented in the plane to construct a continuous in-plane thermal conductive network, so that the composite material has good thermal conductivity.

[0092] The above embodiment is only one of the implementation methods that can realize the technical solution of the present invention. The scope of protection claimed by the present invention is not limited only to this embodiment, but also includes changes, replacements and other implementation methods that can be easily thought of by any technician familiar with this technical field within the technical scope disclosed by the present invention.

Claims

1. A method for preparing a boron nitride nanosheet-aramid nanofiber composite film, characterized in that: include: Calcium chloride is dissolved in sodium alginate aqueous solution to obtain Ca 2+ / SA cross-linking solution; The concentration of sodium alginate aqueous solution is 1-2wt%, Ca 2+ Ca / SA cross-linking solution 2+ The concentration is 1-4mmol / L; Adding hexagonal boron nitride to Ca 2+ The SA / BNNS cross-linking solution was pre-infiltrated by magnetic stirring to obtain a pre-infiltrated SA / BNNS solution; the concentration of hexagonal boron nitride was 40-60 mg / mL; the pre-infiltrated SA / BNNS solution was ball milled and washed to obtain a BNNS / water suspension; the ball milling time was 12-24 hours; The BNNS / water suspension was mixed with the ANF / DMSO dispersion to obtain a BNNS / ANF mixed solution; The BNNS / ANF mixed solution was vacuum filtered, dried and hot pressed to obtain a boron nitride nanosheet-aramid nanofiber composite film.

2. The method for preparing a boron nitride nanosheet-aramid nanofiber composite film according to claim 1, characterized in that: The pre-soaked SA / BNNS solution was ball-milled and washed to obtain a BNNS / water suspension, which was washed with deionized water.

3. The method for preparing a boron nitride nanosheet-aramid nanofiber composite film according to claim 1, characterized in that: The concentration of the BNNS / water suspension was 5-10 mg / mL.

4. The method for preparing a boron nitride nanosheet-aramid nanofiber composite film according to claim 1, characterized in that: The preparation process of ANF / DMSO dispersion is as follows: Para-PPTA fibers and potassium hydroxide were dispersed in DMSO and stirred continuously to obtain an ANF / DMSO dispersion.

5. The method for preparing a boron nitride nanosheet-aramid nanofiber composite film according to claim 1, characterized in that: The concentration of ANF / DMSO dispersion was 1-5 mg / mL.

6. The method for preparing a boron nitride nanosheet-aramid nanofiber composite film according to claim 1, characterized in that: The preparation process of sodium alginate aqueous solution is as follows: Sodium alginate is added into deionized water, stirred and dissolved to obtain a sodium alginate aqueous solution.

7. A boron nitride nanosheet-aramid nanofiber composite film, characterized in that: The boron nitride nanosheet-aramid nanofiber composite film is prepared using the preparation method of any one of claims 1 to 6.

8. The boron nitride nanosheet-aramid nanofiber composite film according to claim 7, characterized in that: The thermal conductivity of the boron nitride nanosheet-aramid nanofiber composite film is 23.86-27.57 W·m -1 ·K -1 .

Images