CN111607229A - High-thermal-conductivity low-friction-coefficient polyphenylene sulfide/boron nitride composite material - Google Patents
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Abstract
The invention discloses a high-thermal-conductivity low-friction-coefficient polyphenylene sulfide/boron nitride (PPS/BN) composite material and a preparation method thereof. The method comprises the steps of tightly and uniformly coating BN micro-pieces on the surfaces of PPS particles in a short time with the aid of absolute ethyl alcohol, then performing hot press molding at 320-330 ℃ and 200-1200 MPa, and constructing an isolation network structure with the BN micro-pieces directionally distributed among the PPS particles in the material, so that a BN three-dimensional heat-conducting network structure is constructed. In addition, based on the self-lubricating property of the PPS and the BN and the better interface interaction of the PPS and the BN, the PPS/BN composite material finally shows excellent heat conduction and friction performance at the same time.
Description
Technical Field
The invention relates to a polyphenylene sulfide composite material and a preparation method thereof, in particular to a polyphenylene sulfide/boron nitride composite material with high heat conductivity and low friction coefficient and a preparation method thereof, belonging to the field of multifunctional composite material preparation.
Background
Polyphenylene Sulfide (PPS) is a special engineering plastic with excellent comprehensive performance, has good high-temperature stability, self-lubricating property, friction property and corrosion resistance, and is widely applied to the fields of war industry, aerospace, automobile industry, electronics and electricity and the like. The friction coefficient is between 0.35 and 0.5, which is not enough to meet the application requirement under the severe friction condition. Therefore, in order to reduce the friction coefficient, most researchers have added solid lubricating substances to the PPS matrix, such as: graphite, polytetrafluoroethylene, MoS2Ceramic particles, and the like.
Friction components, such as gears and bearings, can generate a large amount of heat when subjected to a large frictional force during operation. If the heat cannot be conducted in time, the fatigue wear of the device is aggravated, and the service life of the device is finally reduced. In order to improve the heat conductivity of PPS, high heat conductivity fillers are generally introduced into a matrix, such as: boron Nitride (BN), Carbon Fiber (CF), Graphene (GNP), and the like. Deng et al melt-blend GNP as a modified filler with PPS to prepare a PPS/GNP composite. At 30 ℃ and 30wt% GNP, the thermal conductivity of the PPS/GNP composite material is 1.156W/(m.K), which is about 5 times that of pure PPS [ 0.219W/(m.K) ]. (Deng, S., et al. Journal of Thermal Analysis and calibration, 2014.118(1): p. 197-203.). Kim and the like use an epoxy adhesive layer to coat the heat-conductive BN filler on the surface of the PPS particles, and then heat-press it to convert it into a composite film. When 18 wt% BN was added, the thermal conductivity of PPS increased from 0.28W/(mK) to 1.32W/(mK). (Kim, K. and J. Kim. Composites Science and Technology, 2016.134: p.209-216.). Due to the presence of the epoxy layer, the interfacial thermal resistance is increased and the thermal conductivity is still less than ideal even at higher BN filler contents. The effective construction of the three-dimensional BN heat-conducting network structure is reported to greatly improve the heat-conducting property of the polymer.
At present, researchers have carried out a series of works on wear-resistant PPS and high-thermal conductivity PPS composite materials, but reports of PPS composite materials with high thermal conductivity and low friction coefficient are less. Chinese patent CN104212170A discloses a highly heat-conductive wear-resistant polyphenylene sulfide composite material and a preparation method thereof. The PPS composite material with the heat-conducting filler of Carbon Nano Tubes (CNT) and Carbon Fibers (CF) is prepared by extrusion blending and injection molding. The composite material is insufficient in wear resistance due to the addition of more fillers; also, high levels of CNTs tend to agglomerate, which can lead to non-uniformity in sample properties.
Disclosure of Invention
The invention aims to provide a PPS/BN composite material with high heat conductivity and low friction coefficient and a preparation method thereof. The PPS particles and the BN micro-pieces are uniformly mixed by a simple and unique blending mode, the addition amount of BN is accurately controlled, then a three-dimensional BN heat-conducting network is constructed in the PPS matrix by adopting a specific pressing process, and finally the PPS/BN composite material with high heat conductivity and low friction coefficient is obtained.
The specific implementation method comprises the following steps: the PPS/BN composite material comprises 70-85 parts by mass of PPS and 15-30 parts by mass of BN; the preparation method comprises the steps of tightly and uniformly coating BN micro-pieces on the surfaces of PPS particles in a short time with the aid of absolute ethyl alcohol, and then performing hot press molding at 320-330 ℃ and 200-1200 MPa, so that an isolation network structure with the BN micro-pieces directionally distributed among the PPS particles is constructed in the material, and a BN three-dimensional heat-conducting network structure is constructed.
The BN micro-sheet is added to serve as a heat-conducting filler and a solid lubricant, so that the heat-conducting and friction properties of the PPS can be improved simultaneously. The PPS surface is coated under the auxiliary action of absolute ethyl alcohol, and a three-dimensional heat-conducting isolation network structure is constructed. High thermal conductivity and low coefficient of friction of the composite are achieved at lower filler content.
The PPS used as a matrix is PPS granules with the average grain diameter of 1.39 mm after crushing and screening, and the BN is BN micro-pieces with the average size of 30 mu m.
The more specific preparation method comprises the following steps:
(1) mixing of PPS particles with BN: adding a certain amount of PPS particles and 20 wt% of absolute ethyl alcohol into a container at normal temperature, only wetting the surfaces of the PPS particles, adding BN in batches, and fully stirring each time until the surfaces are uniformly covered with a layer of BN, wherein no BN wall is hung on the inner wall of the container; the mixture is ready to use after mixing;
(2) preparing the PPS/BN composite material by a hot pressing method: carrying out hot pressing on the particles mixed in the step (1), wherein the hot pressing process conditions are as follows: and (3) applying pressure of 200-1200 MPa at 320-330 ℃, keeping the temperature and the pressure for 15-20 min, then cooling to 200-220 ℃ by air cooling, removing the pressure, and continuing air cooling to room temperature.
In the preparation method of the PPS/BN composite material, absolute ethyl alcohol is used as an auxiliary effect, and BN micro-pieces are adhered to the surface of PPS to form an isolation structure.
In the PPS/BN composite material and the preparation method thereof, the PPS/BN composite material comprises 70 parts by mass of PPS and 30 parts by mass of BN, and the high-pressure forming pressure is controlled to be 200-800 MPa.
Uniformly coating the BN microchip on the surface of PPS particles by adopting ethanol to obtain PPS/BN composite particles, and then performing hot press molding to construct a BN three-dimensional heat-conducting network structure. Higher thermal conductivity can be obtained at lower BN content (15-30 parts by mass). In addition, BN is used as a lubricant, a transfer film can be quickly formed on the surface of a workpiece during friction, the friction coefficient is greatly reduced, and the wear resistance is improved. When the BN content is 30 parts, the thermal conductivity of the composite material can be as high as 4.794W/(m.K), the thermal conductivity is improved by 20 times compared with that of pure PPS, and the friction coefficient is as low as 0.18. Toxic solvents are not needed in the experimental process, the material preparation is more environment-friendly, and the process is simpler.
In addition, the invention also has the following advantages:
1) the components of the patent are simple, and the selected raw materials are all commercial products. The heat conductivity of the composite material is remarkably improved at a lower addition amount of BN, and the friction coefficient is greatly reduced.
2) The required equipment of this patent is simple, and used mould can design and the cost is lower according to actual need.
3) The method is easy to implement, simple in equipment maintenance and cleaning and free of harsh requirements on environmental conditions.
4) The method is environment-friendly, and the used raw materials do not relate to chemical pretreatment and do not have the volatilization problem of a solvent.
Drawings
FIG. 1 is surface and cross-sectional SEM images of samples of comparative example 1 (a, c) and example 7 (b, d).
FIGS. 2 a and b are the ultradepth of field micrographs of the samples of comparative example 1 and example 7 after surface rubbing, respectively; c is an optical micrograph of example 7 showing a clear, isolated, three-dimensional thermally conductive network.
FIG. 3 is a graph of the thermal conductivity of PPS/BN composite at different contents of BN at different pressures.
FIG. 4 shows the coefficient of friction of PPS/BN composite at different contents of BN at different pressures.
DETAILED DESCRIPTION OF EMBODIMENT (S) OF INVENTION
The following examples are given to illustrate the present invention and it should be noted that the following examples are only for illustrative purposes and should not be construed as limiting the scope of the present invention, and the non-essential modifications and variations of the present invention by those skilled in the art according to the above disclosure will still fall within the scope of the present invention.
Examples 1 to 12:
(1) mixing of PPS particles with BN: at normal temperature, quantitative PPS particles (PPS-hb, Sichuan Dayangyang New Special Material Co., Ltd.) with an average particle size of 1.39 mm and 20 wt% of absolute ethyl alcohol (AR, Guangdong Guanghua science and technology Co., Ltd.) are added into a container, the surface of the PPS particles is wetted, and the PPS/BN composite materials with different proportions are obtained by adding BN micro-pieces with an average size of 30 mu m according to the mass ratio of BN (BBN-30, product of Yaanbai high New Material Co., Ltd.) to the PPS matrix of 15:85 and 30: 70. In the process, weighed BN needs to be added in batches, the materials are added each time and are fully stirred until the surface is uniformly covered with a layer of BN, no BN wall is hung on the inner wall of the container, and the mixture needs to be mixed and used immediately.
(2) Preparing the PPS/BN composite material by a hot pressing method: carrying out hot pressing on the particles mixed in the step (1), wherein the hot pressing process conditions are as follows: heating the mold from room temperature to 320-330 ℃ through a heating sleeve, respectively pressurizing to 200, 400, 600, 800, 1000 and 1200 MPa, preserving heat and pressure for 15-20 min, then cooling to 200-220 ℃, removing pressure, continuing cooling to room temperature, and opening the mold to obtain the product.
Comparative examples 1 to 6:
adding PPS particles with the particle size of 1.39 mm into a mold cavity, heating the mold from room temperature to 320-330 ℃ through a heating sleeve, respectively pressurizing to 200, 400, 600, 800, 1000 and 1200 MPa, preserving heat and pressure for 15-20 min, then cooling to 200-220 ℃ by air cooling, removing pressure, and continuing air cooling to room temperature to obtain a pure sample containing no BN.
Table 1 examples 1-12 and comparative examples 1-6 formula tables:
TABLE two different PPS/BN composite material heat conductivity, friction coefficient statistical table
The thermal conductivity of the inventive samples was measured at room temperature using a Hot Disk thermal constant analyzer. The test results show that the thermal conductivity is as high as 4.794W/(m.K) (example 12) when the forming pressure is 200 MPa and the BN content is 30wt%, which is improved by 20 times compared with pure PPS (0.24W/(m.K)). BN is coated on the surfaces of PPS particles, and then hot pressing is carried out, so that a heat conduction network of BN can be formed in the PPS matrix, and the heat conduction enhancement effect of the filler is exerted to the maximum extent.
The coefficient of friction of all samples of the invention was tested using a HT-1000 pin-disk high temperature friction wear tester (load 670 g, speed 1000 r/min). When the pressure was 200 MPa and the BN content was 30wt%, the coefficient of friction was as low as 0.18 (example 12), which was 57% lower than that of the pure sample (0.42), and the frictional properties were greatly improved. The BN micro-sheet is flatly paved on the surface of the composite material under the higher forming pressure, so that the self-lubricating capability of the sample is greatly improved, and the friction coefficient of the material is greatly reduced.
Claims (5)
1. A high-thermal-conductivity low-friction-coefficient PPS/BN composite material and a preparation method thereof are characterized in that: the composite material comprises 70-85 parts of PPS and 15-30 parts of BN; the preparation method comprises the steps of tightly and uniformly coating BN micro-pieces on the surfaces of PPS particles in a short time with the aid of absolute ethyl alcohol, and then performing hot press molding at 320-330 ℃ and 200-1200 MPa, so that an isolation network structure with the BN micro-pieces directionally distributed among the PPS particles is constructed in the material, and a BN three-dimensional heat-conducting network structure is constructed.
2. The PPS/BN composite material with high thermal conductivity and low friction coefficient and the preparation method thereof as claimed in claim 1, wherein the PPS as the matrix is PPS pellets with an average particle size of 1.39 mm after crushing and screening, and the BN is BN micro-flakes with an average size of 30 μm.
3. The PPS/BN composite material with high thermal conductivity and low friction coefficient and the preparation method thereof according to claim 1 are characterized in that the preparation method comprises the following steps:
mixing of PPS particles with BN: adding a certain amount of PPS particles and 20 wt% of absolute ethyl alcohol into a container at normal temperature, only wetting the surfaces of the PPS particles, adding BN in batches, and fully stirring each time until the surfaces are uniformly covered with a layer of BN, wherein no BN wall is hung on the inner wall of the container; the mixture is ready to use after mixing;
preparing the PPS/BN composite material by a hot pressing method: carrying out hot pressing on the particles mixed in the step (1), wherein the hot pressing process conditions are as follows: and (3) applying pressure of 200-1200 MPa at 320-330 ℃, keeping the temperature and the pressure for 15-20 min, then cooling to 200-220 ℃ by air cooling, removing the pressure, and continuing air cooling to room temperature.
4. The PPS/BN composite material with high thermal conductivity and low friction coefficient and the preparation method thereof as claimed in claim 3, wherein absolute ethyl alcohol is used as an auxiliary effect to adhere BN micro-pieces on the surface of PPS to form an isolation structure.
5. The PPS/BN composite material with high thermal conductivity and low friction coefficient and the preparation method thereof according to claim 3 are characterized in that the components comprise 70 parts by mass of PPS and 30 parts by mass of BN, and the high-pressure forming pressure is controlled to be 200-800 MPa.
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CN113025041A (en) * | 2021-04-13 | 2021-06-25 | 南京翌动新材料科技有限公司 | Preparation method of high-thermal-conductivity ceramic polymer composite material |
CN113337130A (en) * | 2021-04-12 | 2021-09-03 | 四川大学 | Isolated network composite material containing hybrid nano-filler, preparation method and application thereof |
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CN102558862B (en) * | 2010-12-14 | 2015-07-01 | 合肥杰事杰新材料股份有限公司 | Polyphenylene sulfide composite material and preparation method thereof |
EP2492303A1 (en) * | 2011-02-23 | 2012-08-29 | Berchtold Holding GmbH | Hexagonale boron nitride containing polymer composition |
CN103435998B (en) * | 2013-09-11 | 2016-01-06 | 四川大学 | A kind of method preparing high-ductility heat conduction functional composite material |
CN103554913A (en) * | 2013-10-31 | 2014-02-05 | 广东顺德鸿塑高分子材料有限公司 | Insulation thermal conductive polyphenylene sulfide composite material and preparation method thereof |
CN105062072A (en) * | 2015-09-01 | 2015-11-18 | 东莞市华盈新材料有限公司 | Polyphenyl thioether composite material and preparation method thereof |
CN105255183A (en) * | 2015-09-16 | 2016-01-20 | 蚌埠高华电子股份有限公司 | Magnesium oxide whisker-nanometer boron nitride filling-modified PPS/PBT composite thermal conductive plastic for LEDs and preparation method thereof |
CN105985639A (en) * | 2016-01-07 | 2016-10-05 | 蚌埠高华电子股份有限公司 | Nano lanthanum oxide modified hydrotalcite powder enhanced polyphenylene sulfide-based heat dissipating material for LED and preparation method of nano lanthanum oxide modified hydrotalcite powder enhanced polyphenylene sulfide-based heat dissipating material |
CN105646986A (en) * | 2016-03-01 | 2016-06-08 | 西南科技大学 | Thermally-conductive and insulating polymer composite material with three-dimensional isolation structure and preparation method of thermally-conductive and insulating polymer composite material |
CN106977830B (en) * | 2017-04-24 | 2019-01-25 | 四川大学 | Thermal conductive polymer composite material and preparation method with isolation dual network structure |
CN110408203A (en) * | 2019-07-11 | 2019-11-05 | 西北工业大学 | High thermal conductivity polyimides/boron nitride PI/BN composite material and preparation method with isolation network structure |
CN110564259B (en) * | 2019-08-01 | 2020-09-11 | 厦门大学 | Preparation method of self-lubricating coating material with micro-nano ball effect |
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CN113337130A (en) * | 2021-04-12 | 2021-09-03 | 四川大学 | Isolated network composite material containing hybrid nano-filler, preparation method and application thereof |
CN113025041A (en) * | 2021-04-13 | 2021-06-25 | 南京翌动新材料科技有限公司 | Preparation method of high-thermal-conductivity ceramic polymer composite material |
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