CN117757263A - A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use - Google Patents

A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use Download PDF

Info

Publication number
CN117757263A
CN117757263A CN202410016434.4A CN202410016434A CN117757263A CN 117757263 A CN117757263 A CN 117757263A CN 202410016434 A CN202410016434 A CN 202410016434A CN 117757263 A CN117757263 A CN 117757263A
Authority
CN
China
Prior art keywords
carbon fiber
friction
composite material
wear
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202410016434.4A
Other languages
Chinese (zh)
Inventor
邹华维
李吉祥
周生态
梁梅
衡正光
雷雪
孙晓培
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sichuan University
Original Assignee
Sichuan University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sichuan University filed Critical Sichuan University
Priority to CN202410016434.4A priority Critical patent/CN117757263A/en
Publication of CN117757263A publication Critical patent/CN117757263A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention provides a high-strength low-friction wear-resistant resin matrix composite material, and a preparation method and application thereof, and belongs to the field of composite materials. According to the invention, the irradiation modified polytetrafluoroethylene nano powder is used as a solid lubricant, and the multi-scale chopped carbon fiber is used for compounding and filling in the PPS composite material to construct a compact filler reinforced network structure, so that the obtained composite material has excellent mechanical property and heat conduction property, and simultaneously has excellent low-friction wear-resisting function. The high-strength low-friction wear-resistant resin matrix composite material has very wide application prospect in the fields of aerospace, transportation, electronic devices, high-end mechanical equipment and the like, and can be used for preparing parts such as wear-resistant bearings, self-lubricating parts, mechanical gaskets and the like used under dry friction and other application working conditions.

Description

一种高强度低摩擦耐磨树脂基复合材料及其制备方法和用途A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use

技术领域Technical field

本发明属于复合材料领域,具体涉及一种高强度低摩擦耐磨树脂基复合材料及其制备方法和用途。The invention belongs to the field of composite materials, and specifically relates to a high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use.

背景技术Background technique

众所周知,摩擦磨损现象在日常生活和工业生产中随处可见。在某些情况下,摩擦对于机械系统的正常运转起着至关重要的作用,但周期性的摩擦通常会导致严重的能源损耗和材料磨损,进而大大缩短机械设备及相关零部件的服役寿命。因此,减少各种形式下不利的摩擦磨损,提升材料的自润滑耐磨性能已成为节约能源和提高机械设备可靠性的重要措施。当前,树脂基复合材料具有质量轻、成本低、比强度高、易加工成型等优点,使其在许多领域逐渐取代金属和陶瓷等材料,特别是在摩擦学领域中被广泛应用,如齿轮、轴承、滑轮以及医用器材等。As we all know, friction and wear phenomena can be seen everywhere in daily life and industrial production. In some cases, friction plays a vital role in the normal operation of mechanical systems, but periodic friction often leads to severe energy loss and material wear, which greatly shortens the service life of mechanical equipment and related parts. Therefore, reducing unfavorable friction and wear in various forms and improving the self-lubricating and wear-resistant properties of materials have become important measures to save energy and improve the reliability of mechanical equipment. Currently, resin-based composite materials have the advantages of light weight, low cost, high specific strength, and easy processing and molding, making them gradually replace materials such as metals and ceramics in many fields. They are especially widely used in the field of tribology, such as gears, Bearings, pulleys and medical equipment, etc.

聚苯硫醚(PPS)是一种具有高刚性、高结晶度的线性热塑性树脂,被认为是第六大特种工程塑料。凭借其优异的热力学性能、电学性能、尺寸稳定性和耐化学性,PPS及其复合材料在航空航天、交通运输、机械部件、电子器件及家用设备等领域中得到广泛应用。然而,由于PPS自身具有较高的摩擦系数(0.45-0.57)和高磨损率(3.55×10-3mm3/Nm),其所制备的零部件在使用过程中受极端负载、频繁启停操作等影响易发生剧烈的摩擦磨损,导致其无法满足机械设备中摩擦结构件的应用需求。可见,通过改善PPS的摩擦磨损性能来制备高强度低摩擦耐磨功能复合材料及制件,具有重要的科学价值和应用前景。Polyphenylene sulfide (PPS) is a linear thermoplastic resin with high rigidity and high crystallinity, and is considered the sixth largest special engineering plastic. With its excellent thermodynamic properties, electrical properties, dimensional stability and chemical resistance, PPS and its composite materials are widely used in aerospace, transportation, mechanical components, electronic devices and household equipment and other fields. However, since PPS itself has a high friction coefficient (0.45-0.57) and a high wear rate (3.55×10 -3 mm 3 /Nm), the parts prepared by it are subject to extreme loads and frequent start and stop operations during use. Such effects are prone to severe friction and wear, making it unable to meet the application requirements of friction structural parts in mechanical equipment. It can be seen that improving the friction and wear properties of PPS to prepare high-strength, low-friction and wear-resistant functional composite materials and parts has important scientific value and application prospects.

为推动PPS及其复合材料在机械工程领域的应用,国内外学者们对其摩擦磨损改性进行了大量尝试,然而,目前的技术方法大多忽略了材料的热力学性能及其在极端负载条件下的摩擦学性能,导致材料无法满足实际应用中对机械设备零部件的性能要求。如公开号CN115785671A的专利申请公开了一种气凝胶/聚苯硫醚自润滑摩擦材料及其制备方法,该发明采用气凝胶、增强纤维和液相辅助剂对PPS进行混合填充改性,但其对自润滑性能的改善程度有限(摩擦系数最低为0.178),同时机械强度和导热性能不理想。公开号为CN113337130A的专利申请公开了一种含有杂化纳米填料的隔离网络复合材料、其制备方法及其用途,该发明利用多巴胺的自聚或多巴胺聚醚酰亚胺的共聚合反应在PPS表面共沉积接枝碳纳米管,然后再包裹碳化硅纳米颗粒制备得到一种高导热PPS基复合材料,通过大幅降低摩擦温度来减轻PPS的摩擦磨损,但该方法对PPS摩擦学性能的改善程度有限(摩擦系数最低为0.193,比磨损率为2.50×10-5mm3/Nm)。公开号为CN109370220A的专利申请公开了一种石墨烯改性聚苯硫醚复合材料及其制备方法,该发明主要采用石墨烯粉末、玄武岩纤维、固化剂和硫化剂对PPS进行改性,通过该方法极大地降低了PPS的摩擦系数和磨损率,但其力学强度差,难以在实际应用中发挥作用。因此,开发一种兼具优异机械强度和高导热性能的自润滑耐磨树脂基复合材料及其制备方法具有重要的科学价值和应用前景。In order to promote the application of PPS and its composite materials in the field of mechanical engineering, domestic and foreign scholars have made a lot of attempts to modify their friction and wear. However, current technical methods mostly ignore the thermodynamic properties of the material and its behavior under extreme load conditions. Tribological properties result in materials that cannot meet the performance requirements for mechanical equipment parts in practical applications. For example, the patent application with publication number CN115785671A discloses an airgel/polyphenylene sulfide self-lubricating friction material and its preparation method. This invention uses airgel, reinforcing fiber and liquid phase auxiliary agent to mix and fill modified PPS. However, its improvement in self-lubricating performance is limited (the lowest friction coefficient is 0.178), and its mechanical strength and thermal conductivity are not ideal. The patent application with publication number CN113337130A discloses an isolation network composite material containing hybrid nanofillers, its preparation method and its use. This invention utilizes the self-polymerization of dopamine or the copolymerization of dopamine polyetherimide on the surface of PPS A highly thermally conductive PPS-based composite material is prepared by co-depositing grafted carbon nanotubes and then wrapping silicon carbide nanoparticles. It reduces the friction and wear of PPS by significantly reducing the friction temperature. However, this method has limited improvement in the tribological properties of PPS. (The lowest friction coefficient is 0.193, and the specific wear rate is 2.50×10 -5 mm 3 /Nm). The patent application with publication number CN109370220A discloses a graphene-modified polyphenylene sulfide composite material and its preparation method. The invention mainly uses graphene powder, basalt fiber, curing agent and vulcanizing agent to modify PPS. Through this This method greatly reduces the friction coefficient and wear rate of PPS, but its poor mechanical strength makes it difficult to play a role in practical applications. Therefore, the development of a self-lubricating and wear-resistant resin-based composite material with excellent mechanical strength and high thermal conductivity and its preparation method has important scientific value and application prospects.

发明内容Contents of the invention

本发明的目的在于提供一种高强度低摩擦耐磨树脂基复合材料及其制备方法和用途。The object of the present invention is to provide a high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use.

本发明提供了一种高强度低摩擦耐磨树脂基复合材料,它是由以下重量份数的原料制备得到的:树脂基体10-200份,固体润滑剂5-80份,碳纤维1-60份;所述碳纤维包括碳纤维A和碳纤维B,碳纤维A的平均长度为0.1-3mm,平均直径为1-20μm,碳纤维B的平均长度为1-20mm,平均直径为1-20μm。The invention provides a high-strength, low-friction and wear-resistant resin-based composite material, which is prepared from the following raw materials in parts by weight: 10-200 parts of resin matrix, 5-80 parts of solid lubricant, and 1-60 parts of carbon fiber. ; The carbon fiber includes carbon fiber A and carbon fiber B. The average length of carbon fiber A is 0.1-3mm and the average diameter is 1-20μm. The average length of carbon fiber B is 1-20mm and the average diameter is 1-20μm.

进一步地,所述高强度低摩擦耐磨树脂基复合材料是由以下重量份数的原料制备得到的:树脂基体20-100份,固体润滑剂10-50份,碳纤维10-40份;所述碳纤维由碳纤维A和碳纤维B组成,其中碳纤维A和碳纤维B的重量比为(1-3):(1-3)。Further, the high-strength, low-friction and wear-resistant resin-based composite material is prepared from the following raw materials in parts by weight: 20-100 parts of resin matrix, 10-50 parts of solid lubricant, and 10-40 parts of carbon fiber; Carbon fiber is composed of carbon fiber A and carbon fiber B, where the weight ratio of carbon fiber A and carbon fiber B is (1-3): (1-3).

进一步地,所述高强度低摩擦耐磨树脂基复合材料是由以下重量份数的原料制备得到的:树脂基体56份,固体润滑剂24份,碳纤维20份;所述碳纤维由碳纤维A和碳纤维B组成,其中碳纤维A和碳纤维B的重量比为1:3。Further, the high-strength, low-friction and wear-resistant resin-based composite material is prepared from the following parts by weight of raw materials: 56 parts of resin matrix, 24 parts of solid lubricant, and 20 parts of carbon fiber; the carbon fiber is composed of carbon fiber A and carbon fiber Composed of B, the weight ratio of carbon fiber A and carbon fiber B is 1:3.

进一步地,所述碳纤维A的平均长度为0.2-1mm,平均直径为2-10μm,碳纤维B的平均长度为2-10mm,平均直径为2-10μm。Further, the average length of carbon fiber A is 0.2-1 mm, and the average diameter is 2-10 μm. The average length of carbon fiber B is 2-10 mm, and the average diameter is 2-10 μm.

进一步地,所述碳纤维A的平均长度为0.3mm,平均直径为6μm,碳纤维B的平均长度为3mm,平均直径为7μm。Further, the average length of carbon fiber A is 0.3 mm and the average diameter is 6 μm. The average length of carbon fiber B is 3 mm and the average diameter is 7 μm.

进一步地,所述树脂基体为热塑性树脂;所述固体润滑剂为聚四氟乙烯或其衍生物;所述碳纤维为聚丙烯腈基或沥青基短切碳纤维。Further, the resin matrix is a thermoplastic resin; the solid lubricant is polytetrafluoroethylene or its derivatives; and the carbon fiber is polyacrylonitrile-based or pitch-based chopped carbon fiber.

进一步地,所述树脂基体为聚苯硫醚;所述聚四氟乙烯的衍生物为辐照改性聚四氟乙烯,所述碳纤维为聚丙烯腈基短切碳纤维。Further, the resin matrix is polyphenylene sulfide; the derivative of polytetrafluoroethylene is radiation-modified polytetrafluoroethylene; and the carbon fiber is polyacrylonitrile-based chopped carbon fiber.

本发明还提供了一种制备上述高强度低摩擦耐磨树脂基复合材料的方法,它包括以下步骤:取原料干燥、预混合,熔融共混,即可。通过采用上述方法制备的高强度低摩擦耐磨树脂基复合材料可以选用常规的热压成型、压延成型、(微)注塑成型等热塑性加工手段。The invention also provides a method for preparing the above-mentioned high-strength, low-friction and wear-resistant resin-based composite material, which includes the following steps: drying the raw materials, premixing, and melting and blending. The high-strength, low-friction and wear-resistant resin-based composite materials prepared by the above method can use conventional thermoplastic processing methods such as hot pressing molding, calendering molding, (micro)injection molding, etc.

进一步地,所述成型是注塑成型。Further, the molding is injection molding.

本发明还提供了上述高强度低摩擦聚合物耐磨树脂基复合材料在航空航天、交通运输、电子器件及高端机械装备领域的应用。The invention also provides applications of the above-mentioned high-strength, low-friction polymer wear-resistant resin-based composite materials in the fields of aerospace, transportation, electronic devices and high-end mechanical equipment.

上述高强度低摩擦耐磨树脂基复合材料可用于制备干摩擦及其他工况条件下使用的耐磨轴承、自润滑零件、机械衬垫等零部件。The above-mentioned high-strength, low-friction and wear-resistant resin-based composite materials can be used to prepare wear-resistant bearings, self-lubricating parts, mechanical liners and other parts used under dry friction and other working conditions.

与现有技术相比,本发明取得了以下有益效果:本发明采用辐照改性的聚四氟乙烯纳米粉作为固体润滑剂,利用多尺度的短切碳纤维复配填充在PPS复合材料中构建致密的填料增强网络,使所得复合材料具备优异的机械性能和导热性能,同时促进对偶件表面高润滑转移膜的形成,进而在不同PV工况下均能够表现出优异的摩擦学性能。本发明的高强度低摩擦耐磨树脂基复合材料在航空航天、交通运输、电子器件及高端机械装备等领域具有广阔的应用前景,可用于制备在干摩擦及其他工况条件下使用的耐磨轴承、自润滑零件、机械衬垫等零部件。Compared with the existing technology, the present invention has achieved the following beneficial effects: the present invention uses radiation-modified polytetrafluoroethylene nanopowder as a solid lubricant, and uses multi-scale chopped carbon fiber compound filling to construct in PPS composite materials The dense filler-reinforced network enables the resulting composite material to have excellent mechanical properties and thermal conductivity, and at the same time promotes the formation of a highly lubricating transfer film on the surface of the dual parts, thereby exhibiting excellent tribological properties under different PV operating conditions. The high-strength, low-friction and wear-resistant resin-based composite material of the present invention has broad application prospects in the fields of aerospace, transportation, electronic devices and high-end mechanical equipment, and can be used to prepare wear-resistant materials for use under dry friction and other working conditions. Bearings, self-lubricating parts, mechanical gaskets and other components.

显然,根据本发明的上述内容,按照本领域的普通技术知识和惯用手段,在不脱离本发明上述基本技术思想前提下,还可以做出其它多种形式的修改、替换或变更。Obviously, according to the above content of the present invention, according to the common technical knowledge and common means in the field, without departing from the above basic technical idea of the present invention, various other forms of modifications, replacements or changes can also be made.

以下通过实施例形式的具体实施方式,对本发明的上述内容再作进一步的详细说明。但不应将此理解为本发明上述主题的范围仅限于以下的实例。凡基于本发明上述内容所实现的技术均属于本发明的范围。The above contents of the present invention will be further described in detail below through specific implementation methods in the form of examples. However, this should not be understood to mean that the scope of the above subject matter of the present invention is limited to the following examples. All technologies implemented based on the above contents of the present invention belong to the scope of the present invention.

附图说明Description of the drawings

图1.(A)i-PTFE,(B)PSCF和(C)SCF的形貌图。Figure 1. Morphology images of (A) i-PTFE, (B) PSCF and (C) SCF.

图2.(A)P/i-PTFE,(B)P/i-PTFE/PS20,(C)P/i-PTFE/PS15-S5,(D)P/i-PTFE/PS10-S10,(E)P/i-PTFE/PS5-S15,(F)P/i-PTFE/S20复合材料的脆断面形貌。Figure 2. (A)P/i-PTFE, (B)P/i-PTFE/PS20, (C)P/i-PTFE/PS15-S5, (D)P/i-PTFE/PS10-S10, ( E) Brittle fracture morphology of P/i-PTFE/PS5-S15 and (F) P/i-PTFE/S20 composites.

图3.各树脂基复合材料的(A)弯曲性能、(B)拉伸强度和表面硬度。Figure 3. (A) Flexural properties, (B) tensile strength and surface hardness of each resin-based composite material.

图4.各树脂基复合材料的(A)瞬时摩擦系数、(B)平均摩擦系数和比磨损率。Figure 4. (A) Instantaneous friction coefficient, (B) average friction coefficient and specific wear rate of each resin-based composite material.

图5.(A)P/i-PTFE、(B)P/i-PTFE/P20、(C)P/i-PTFE/PS15-S5、(D)P/i-PTFE/PS10-S10、(E)P/i-PTFE/PS5-S15和(F)P/i-PTFE/S20复合材料的磨损表面形貌图。Figure 5. (A)P/i-PTFE, (B)P/i-PTFE/P20, (C)P/i-PTFE/PS15-S5, (D)P/i-PTFE/PS10-S10, ( E) Wear surface morphology of P/i-PTFE/PS5-S15 and (F) P/i-PTFE/S20 composites.

图6.(A)P/i-PTFE、(B)P/i-PTFE/PS20、(C)P/i-PTFE/PS15-S5、(D)P/i-PTFE/PS10-S10、(E)P/i-PTFE/PS5-S15和(F)P/i-PTFE/S20复合材料的磨痕3D形貌图。Figure 6. (A)P/i-PTFE, (B)P/i-PTFE/PS20, (C)P/i-PTFE/PS15-S5, (D)P/i-PTFE/PS10-S10, ( E) 3D morphology of wear scars of P/i-PTFE/PS5-S15 and (F) P/i-PTFE/S20 composites.

图7.各树脂基复合材料的(A)瞬时摩擦温度和(B)导热系数。Fig. 7. (A) Instantaneous friction temperature and (B) thermal conductivity of various resin-based composites.

图8.各树脂基复合材料在高PV条件下的(A)摩擦系数和(B)比磨损率。图9.销盘式摩擦磨损试验中(A)P/i-PTFE、(B)P/i-PTFE/P20、(C)P/i-PTFE/PS5-S15和(D)P/i-PTFE/S20复合材料的对应钢盘表面转移层形貌。Figure 8. (A) Friction coefficient and (B) specific wear rate of each resin-based composite material under high PV conditions. Figure 9. (A)P/i-PTFE, (B)P/i-PTFE/P20, (C)P/i-PTFE/PS5-S15 and (D)P/i- in pin-on-disk friction and wear test The corresponding transfer layer morphology of the steel plate surface of the PTFE/S20 composite material.

具体实施方式Detailed ways

本发明所用原料与设备均为已知产品,通过购买市售产品所得。The raw materials and equipment used in the present invention are all known products and are obtained by purchasing commercially available products.

聚苯硫醚(PPS)粉末(密度1.35g/cm3,熔融温度285℃),购自德阳科吉高新材料有限责任公司。辐照改性聚四氟乙烯纳米粉(i-PTFE)(牌号为JH-305F,粒径200-300nm)从四川金核高分子材料有限公司购得。WD-30型聚丙烯腈基短碳纤维(PSCF,平均长度0.3mm,平均直径6μm),LSC070-PEEK型聚丙烯腈基短碳纤维(SCF,平均长度3mm,平均直径7μm),均购自上海力硕复合材料科技有限公司。i-PTFE、PSCF和SCF的微观形貌如图1所示。Polyphenylene sulfide (PPS) powder (density 1.35g/cm 3 , melting temperature 285°C) was purchased from Deyang Keji High-tech Materials Co., Ltd. Irradiation-modified polytetrafluoroethylene nanopowder (i-PTFE) (brand name JH-305F, particle size 200-300 nm) was purchased from Sichuan Jinhe Polymer Materials Co., Ltd. WD-30 polyacrylonitrile-based short carbon fiber (PSCF, average length 0.3 mm, average diameter 6 μm), LSC070-PEEK polyacrylonitrile-based short carbon fiber (SCF, average length 3 mm, average diameter 7 μm), both purchased from Shanghai Li Shuo Composite Materials Technology Co., Ltd. The micromorphology of i-PTFE, PSCF and SCF is shown in Figure 1.

实施例1、本发明高强度低摩擦耐磨树脂基复合材料的制备Example 1. Preparation of high-strength, low-friction and wear-resistant resin-based composite materials of the present invention

采用熔融共混法制备树脂基复合材料,具体操作如下:所有原料使用前于80±5℃下干燥12±0.5h。将干燥后的原料按照表1所示的配比进行预混合。然后,利用同向平行双螺杆挤出机(TSSJ/25/33,成都盛达化工有限公司,中国)进行熔融混合。经挤出机均匀塑化,冷却造粒后放置于鼓风干燥箱中干燥12±1h,即得。上述所得的复合材料采用注塑成型机进行注塑加工成型。分别制备得到如下高强度低摩擦耐磨树脂基复合材料:P/i-PTFE/PS20、P/i-PTFE/PS15-S5、P/i-PTFE/PS10-S10、P/i-PTFE/PS5-S15和P/i-PTFE/S20。Resin-based composite materials were prepared using the melt blending method. The specific operations are as follows: all raw materials were dried at 80±5°C for 12±0.5h before use. The dried raw materials are premixed according to the ratio shown in Table 1. Then, melt mixing was performed using a co-rotating parallel twin-screw extruder (TSSJ/25/33, Chengdu Shengda Chemical Co., Ltd., China). It is uniformly plasticized by the extruder, cooled and granulated, and then placed in a blast drying oven to dry for 12±1h. The composite material obtained above is injection molded using an injection molding machine. The following high-strength, low-friction and wear-resistant resin-based composite materials were prepared respectively: P/i-PTFE/PS20, P/i-PTFE/PS15-S5, P/i-PTFE/PS10-S10, P/i-PTFE/PS5 -S15 and P/i-PTFE/S20.

表1.原料配比Table 1. Raw material ratio

注:表1中30重量份用量为300g。Note: The dosage of 30 parts by weight in Table 1 is 300g.

以下为对照样品的制备方法。The following is how to prepare the control sample.

对照例1、自润滑树脂基复合材料的制备Comparative Example 1. Preparation of self-lubricating resin matrix composite material

按照实施例1的方法,按照表1所示的原料配比制备得到自润滑树脂基复合材料(P/i-PTFE)。According to the method of Example 1, a self-lubricating resin-based composite material (P/i-PTFE) was prepared according to the raw material ratio shown in Table 1.

以下通过实验例证明本发明的有益效果。The beneficial effects of the present invention are demonstrated below through experimental examples.

实验例1、各树脂基复合材料的断截面微观形貌表征Experimental Example 1. Characterization of microscopic morphology of cross-sections of various resin-based composite materials

(1)实验方法(1) Experimental methods

采用SEM扫描电镜(JSM-9600,日本)对各树脂基复合材料的脆断面进行观察。SEM scanning electron microscope (JSM-9600, Japan) was used to observe the brittle fracture surfaces of each resin-based composite material.

(2)实验结果(2)Experimental results

图2显示了各树脂基复合材料的断截面微观形貌。如图2(A)所示,在P/i-PTFE中观察到明显的孔洞和i-PTFE颗粒团聚体,这表明i-PTFE填充会在复合材料中形成缺陷。此外,P/i-PTFE的断裂形貌非常光滑,这表明复合材料具有脆性特征。图2(B~F)显示了P/i-PTFE/CFs复合材料的断截面微观形貌。结果表明,碳纤维(CFs)在PPS基体内部随机分散并相互缠绕形成了“钢筋混凝土”式增强结构。此外,还观察到因外力作用导致CFs剥离而产生的空洞或痕迹。但随着SCF含量的增加,P/i-PTFE/CFs复合材料断裂面观察到的空洞或缺陷越来越少。这是因为低长径比PSCF在复合材料内形成了松散的填料网络结构,而这种松散的结构往往会被外力破坏,从而在断裂表面形成更多缺陷,尤其是P/i-PTFE/PS20。相反,随着高长径比SCF含量的增加,会形成更多的互穿网络结构,这种结构能够抵御外力,有利于提高机械性能。当PSCF与SCF添加比例为1:3时,复合材料的断截面表现出最少的缺陷,这是由于一定含量的PSCF可以有效填补SCF间的间隙,从而减少贫纤区,使聚合物基体在碳纤维互穿网络下表现出更致密的形貌。Figure 2 shows the cross-sectional micromorphology of each resin-based composite material. As shown in Figure 2(A), obvious pores and i-PTFE particle agglomerates were observed in P/i-PTFE, indicating that i-PTFE filling would form defects in the composite. In addition, the fracture morphology of P/i-PTFE is very smooth, which indicates that the composite has brittle characteristics. Figure 2(B~F) shows the cross-sectional micromorphology of P/i-PTFE/CFs composite material. The results show that carbon fibers (CFs) are randomly dispersed and intertwined within the PPS matrix to form a "reinforced concrete" reinforced structure. In addition, voids or traces caused by exfoliation of CFs due to external force were also observed. However, as the SCF content increases, fewer and fewer voids or defects are observed on the fracture surface of P/i-PTFE/CFs composites. This is because low aspect ratio PSCF forms a loose filler network structure within the composite material, and this loose structure is often destroyed by external forces, thereby forming more defects on the fracture surface, especially P/i-PTFE/PS20 . On the contrary, as the high aspect ratio SCF content increases, more interpenetrating network structures will be formed, which can resist external forces and help improve mechanical properties. When the addition ratio of PSCF to SCF is 1:3, the fracture section of the composite material shows the least defects. This is because a certain content of PSCF can effectively fill the gaps between SCF, thus reducing the fiber-poor area and making the polymer matrix in the carbon fiber. The interpenetrating network shows a denser morphology.

实验例2、各树脂基复合材料的机械性能表征Experimental Example 2. Characterization of mechanical properties of each resin matrix composite material

(1)实验方法(1) Experimental methods

采用万能材料试验机(Instron 5567,美国)在室温下对各树脂基复合材料的力学性能进行测试。按照GB/T 1040.2-2022标准进行拉伸强度测试,样品尺寸为150×10×4mm3,测试速度采用10mm/min。按照GB/T9341-2008标准进行弯曲性能测试,样品尺寸:80×10×4mm3,测试速度:2mm/min。A universal material testing machine (Instron 5567, USA) was used to test the mechanical properties of each resin-based composite material at room temperature. The tensile strength test was carried out in accordance with the GB/T 1040.2-2022 standard. The sample size was 150×10×4mm 3 and the test speed was 10mm/min. The bending performance test was carried out in accordance with the GB/T9341-2008 standard, sample size: 80×10×4mm 3 , test speed: 2mm/min.

使用HANDPILX-D邵氏硬度计(乐清市HANDPI仪器有限公司,中国)对各树脂基复合材料的表面硬度进行了测试。The surface hardness of each resin-based composite material was tested using a HANDPILX-D Shore hardness tester (Yueqing HANDPI Instrument Co., Ltd., China).

(2)实验结果(2)Experimental results

图3显示了各树脂基复合材料的机械性能,包括弯曲性能、拉伸强度和表面硬度。图3(A)表明,随着CFs的添加,复合材料的弯曲强度和弯曲模量均显著增加。当PSCF/SCF质量比为1:3时,材料的弯曲强度和模量均达到最大值。即,P/i-PTFE/PS5-S15的弯曲强度和模量分别达到191.1MPa和13.7GPa,比P/i-PTFE高出125.6%和389.3%。因此,不同长径比CFs杂化有利于改善复合材料的弯曲性能。图3(B)显示了含有不同CFs的树脂基复合材料的拉伸强度和表面硬度。与弯曲性能类似,PPS/i-PTFE/CF复合材料的拉伸强度随着CFs的添加而显著增加,并且拉伸强度值随着SCF含量的增加而持续增加。这归因于高长径比CFs具有更好的增强作用,从而提高了复合材料的拉伸强度。此外,图3(B)显示,添加CFs后,树脂基复合材料的表面硬度得到提高,这与形成的缠结CFs网络结构导致其表面硬度提高有关。上述实验结果表明,P/i-PTFE/CFs复合材料的机械性能和表面硬度同时提高。Figure 3 shows the mechanical properties of each resin matrix composite, including bending properties, tensile strength and surface hardness. Figure 3(A) shows that with the addition of CFs, both the flexural strength and flexural modulus of the composite material increase significantly. When the mass ratio of PSCF/SCF is 1:3, the bending strength and modulus of the material reach their maximum values. That is, the flexural strength and modulus of P/i-PTFE/PS5-S15 reach 191.1MPa and 13.7GPa respectively, which are 125.6% and 389.3% higher than P/i-PTFE. Therefore, hybridization of CFs with different aspect ratios is beneficial to improving the bending properties of composite materials. Figure 3(B) shows the tensile strength and surface hardness of resin-based composites containing different CFs. Similar to the flexural properties, the tensile strength of PPS/i-PTFE/CF composites increases significantly with the addition of CFs, and the tensile strength value continues to increase with the increase of SCF content. This is attributed to the better reinforcement effect of high aspect ratio CFs, thereby improving the tensile strength of the composite. In addition, Figure 3(B) shows that the surface hardness of the resin matrix composite is improved after adding CFs, which is related to the formation of entangled CFs network structure that leads to an increase in surface hardness. The above experimental results show that the mechanical properties and surface hardness of P/i-PTFE/CFs composite materials are simultaneously improved.

实验例3、各树脂基复合材料的摩擦磨损性能表征Experimental Example 3. Characterization of friction and wear properties of various resin-based composite materials

(1)实验方法(1) Experimental methods

按照GB/T3960-2016标准,采用环块式摩擦磨损试验机(M-200,北京冠测实验仪器有限公司)测试各树脂基复合材料在滑动速度为0.42m/s和载荷为200N的工况条件下的摩擦学性能。样品尺寸为30×7×6mm3,采用表面粗糙度Ra=0.8μm的45#钢环为摩擦副。在测试前,用砂纸将钢环表面打磨抛光,并置于丙酮中超声清洗,然后取出自然干燥,每一试样做三次平行实验。复合材料的磨损率采用体积计算法进行测量,测试时间为1h。In accordance with the GB/T3960-2016 standard, a ring-block friction and wear testing machine (M-200, Beijing Guanchai Experimental Instrument Co., Ltd.) was used to test each resin-based composite material under the working conditions of a sliding speed of 0.42m/s and a load of 200N. Tribological properties under conditions. The sample size is 30×7×6mm 3 , and a 45# steel ring with surface roughness Ra=0.8μm is used as the friction pair. Before the test, the surface of the steel ring was polished with sandpaper, ultrasonically cleaned in acetone, and then taken out to dry naturally. Three parallel experiments were conducted on each sample. The wear rate of the composite material was measured using the volume calculation method, and the test time was 1 hour.

瞬时摩擦系数(μ)和比磨损率(SWR)的计算公式分别如下:The calculation formulas of instantaneous friction coefficient (μ) and specific wear rate (SWR) are as follows:

其中,P为摩擦力矩(Nm),F为施加的载荷(N),r为摩擦副的半径(mm),v为磨损体积(mm3),d为样品宽度(mm),w为摩擦试验后样品的磨痕宽度(mm),L为滑动距离(m)。Among them, P is the friction moment (Nm), F is the applied load (N), r is the radius of the friction pair (mm), v is the wear volume (mm 3 ), d is the sample width (mm), and w is the friction test The wear scar width of the final sample (mm), L is the sliding distance (m).

利用SEM扫描电镜(JSM-9600,日本)和三维光学轮廓仪(ContourGT-K,德国)分别对树脂基复合材料在摩擦测试后的磨损面微观形貌和磨痕形态进行观察。The SEM scanning electron microscope (JSM-9600, Japan) and the three-dimensional optical profilometer (ContourGT-K, Germany) were used to observe the micromorphology and wear scar morphology of the wear surface of the resin-based composite material after the friction test.

(2)实验结果(2)Experimental results

图4(A)显示了各树脂基复合材料的瞬时摩擦系数与滑动时间的关系。结果表明,随着CFs的加入,由于断裂的CFs在滑动界面中起到了硬质磨料的作用会导致摩擦前期的摩擦系数不稳定,但SCF形成的增强填料网络结构使其在滑动过程中难以被剥离,有利于降低摩擦过程的波动性。如图4(B)所示,通过对比P/i-PTFE/PS20和P/i-PTFE/S20的平均摩擦系数和比磨损率发现,PSCFs能有效降低摩擦系数,而SCFs则能大大降低比磨损率,结合图5、6中对复合材料磨损表面和磨痕的观察,这是由于前者的易剥离性产生的碎屑促进了润滑转移膜的形成,而后者的高抗外力能力能够极大地减轻材料的磨损程度。当PSCFs和SCFs的填充比例为1:3时,P/i-PTFE/PS5-S15复合材料的平均摩擦系数和比磨损率低至0.142和1.63×10-6mm3/Nm,与P/i-PTFE相比分别提高了13.9%和95.5%,如图5、6和表2所示,P/i-PTFE/PS5-S15复合材料的磨损表面十分光滑并且呈现出最浅最窄的磨痕,这主要是其内部不同长径比CFs之间的协同互补作用形成了完整的增强网络结构,有助于提高复合材料的机械性能和导热性。另外,低长径比PSCFs形成的石墨层与低表面能i-PTFE起到协同润滑效果,从而极大地改善了复合材料的摩擦学性能。Figure 4(A) shows the relationship between the instantaneous friction coefficient and sliding time of each resin-based composite material. The results show that with the addition of CFs, the friction coefficient in the early stage of friction will be unstable because the fractured CFs acts as a hard abrasive in the sliding interface. However, the reinforced filler network structure formed by SCF makes it difficult to be removed during the sliding process. Peeling is beneficial to reducing the volatility of the friction process. As shown in Figure 4(B), by comparing the average friction coefficient and specific wear rate of P/i-PTFE/PS20 and P/i-PTFE/S20, it is found that PSCFs can effectively reduce the friction coefficient, while SCFs can greatly reduce the specific wear rate. Wear rate, combined with the observations of composite wear surfaces and wear scars in Figures 5 and 6, is due to the fact that the debris generated by the easy peelability of the former promotes the formation of the lubrication transfer film, while the high resistance to external forces of the latter can greatly Reduce material wear. When the filling ratio of PSCFs and SCFs is 1:3, the average friction coefficient and specific wear rate of P/i-PTFE/PS5-S15 composite are as low as 0.142 and 1.63×10 -6 mm 3 /Nm, which are similar to those of P/i -PTFE increased by 13.9% and 95.5% respectively. As shown in Figures 5, 6 and Table 2, the wear surface of P/i-PTFE/PS5-S15 composite material is very smooth and shows the shallowest and narrowest wear marks. , this is mainly due to the synergistic and complementary interaction between CFs with different aspect ratios within it to form a complete reinforced network structure, which helps to improve the mechanical properties and thermal conductivity of the composite material. In addition, the graphite layer formed by low aspect ratio PSCFs and low surface energy i-PTFE have a synergistic lubrication effect, thereby greatly improving the tribological properties of the composite material.

表2.各树脂基复合材料磨痕的宽度(Rd)和深度(Rv)Table 2. Width (R d ) and depth (R v ) of wear scars of each resin matrix composite material

样品sample Rd(μm)R d (μm) Rv(μm)R v (μm) P/i-PTEFP/i-PTEF 69276927 318318 P/i-PTFE/PS20P/i-PTFE/PS20 42924292 9999 P/i-PTFE/PS15-S5P/i-PTFE/PS15-S5 66306630 412412 P/i-PTFE/PS10-S10P/i-PTFE/PS10-S10 36773677 117117 P/i-PTFE/PS5-S15P/i-PTFE/PS5-S15 26522652 2929 P/i-PTFE/S20P/i-PTFE/S20 28232823 3333

实验例4、各树脂基复合材料的摩擦热和导热性能表征Experimental Example 4. Characterization of frictional heat and thermal conductivity of each resin-based composite material

(1)实验方法(1) Experimental methods

采用配备了K型热电偶的多路径温度计(AT4204,中国常州安百精密仪器有限公司)实时监测摩擦测试过程中的温度来表征摩擦热。A multipath thermometer (AT4204, Changzhou Anbai Precision Instrument Co., Ltd., Changzhou, China) equipped with a K-type thermocouple was used to real-time monitor the temperature during the friction test to characterize the friction heat.

采用HotDisk热常数分析仪(2500-OT,瑞典)对各树脂基复合材料的导热性能进行了表征。The thermal conductivity properties of each resin-based composite material were characterized using a HotDisk thermal constant analyzer (2500-OT, Sweden).

(2)实验结果(2)Experimental results

图7(A)显示了各树脂基复合材料在摩擦过程中的样品温度随时间的变化情况,可以看到,在500s之前,所有试样的摩擦温度都明显升高,这与磨合阶段摩擦热的积累有关。在这种情况下,一旦试样块与摩擦副接触,摩擦热就开始在滑动界面上产生和积累,从而导致试样的瞬时摩擦温度升高。P/i-PTFE复合材料具有最高的摩擦温度,这说明其在摩擦测试过程中可能遭受到较大的摩擦阻力,从而产生大量摩擦热。由图7(B)可知,P/i-PTFE具有最低的导热系数(0.27W/mK),因此材料在测试过程中产生的大量摩擦热无法有效分散,导致其在摩擦接触面长时堆积,促使聚合物发生一定程度的软化及力学强度的降低,造成严重的表面磨损,这与其较高的摩擦系数和比磨损率相对应。其中,P/i-PTFE/PS5-S15复合材料在摩擦过程中的摩擦温度最低,这归因于以下因素:(1)与其他试样块相比,P/i-PTFE/PS5-S15具有更高的热导率(0.62W/mK),相比于P/i-PTFE提升了129.63%,这有利于在滑动过程中耗散摩擦热,从而避免磨损程度的加剧;(2)良好的转移膜形成减少了复合材料与摩擦副之间的直接接触,从而降低了滑动界面的摩擦功耗。Figure 7(A) shows the change of sample temperature with time during the friction process of each resin-based composite material. It can be seen that before 500s, the friction temperature of all samples increased significantly, which is consistent with the friction heat in the running-in stage. related to the accumulation. In this case, once the specimen block comes into contact with the friction pair, friction heat begins to be generated and accumulated on the sliding interface, resulting in an increase in the instantaneous friction temperature of the specimen. The P/i-PTFE composite material has the highest friction temperature, which indicates that it may encounter large friction resistance during the friction test, thereby generating a large amount of friction heat. As can be seen from Figure 7(B), P/i-PTFE has the lowest thermal conductivity (0.27W/mK), so the large amount of frictional heat generated by the material during the test cannot be effectively dispersed, causing it to accumulate on the friction contact surface for a long time. It causes the polymer to soften to a certain extent and reduce its mechanical strength, causing severe surface wear, which corresponds to its higher friction coefficient and specific wear rate. Among them, the P/i-PTFE/PS5-S15 composite material has the lowest friction temperature during the friction process, which is attributed to the following factors: (1) Compared with other sample blocks, P/i-PTFE/PS5-S15 has Higher thermal conductivity (0.62W/mK), 129.63% higher than P/i-PTFE, which is beneficial to dissipating friction heat during the sliding process, thereby avoiding increased wear; (2) Good The transfer film formation reduces the direct contact between the composite material and the friction pair, thereby reducing the friction power consumption of the sliding interface.

实验例5、各树脂基复合材料在高PV下的摩擦学性能测试Experimental Example 5. Tribological performance test of various resin-based composite materials under high PV

(1)实验方法(1) Experimental methods

采用自制的销盘式摩擦磨损试验装置测试了各树脂基复合材料在滑动速度为2m/s和载荷为200N的工况条件下(PV≥10MPa·m/s)的摩擦学性能。材料的磨损采用称重法进行测量,测试时间为210s,每次测试结束后重新用砂纸打磨钢盘表面并用丙酮清洗待其温度恢复至室温再进行测试。A self-made pin-on-disk friction and wear test device was used to test the tribological properties of each resin-based composite material under the working conditions of a sliding speed of 2m/s and a load of 200N (PV≥10MPa·m/s). The wear of the material was measured using the weighing method, and the test time was 210 seconds. After each test, the surface of the steel plate was re-polished with sandpaper and cleaned with acetone until its temperature returned to room temperature before testing.

PV值指材料和摩擦装置接触面积上的单位载荷P与相对滑动线速度V的乘积,以此近似地衡量材料摩擦测试条件的苛刻程度。The PV value refers to the product of the unit load P on the contact area between the material and the friction device and the relative sliding linear velocity V, which is an approximate measure of the harshness of the material friction test conditions.

(2)实验结果(2)Experimental results

图8(A)和(B)分别显示了使用自制的销盘式摩擦磨损试验装置评估的各树脂基复合材料的摩擦系数和磨损率。高PV下的摩擦学性能测试持续时间为210s,分为五个测试周期,每个周期持续42s。如图8(A)所示,所有样品在高PV下的摩擦系数都随着测试周期的增加而降低,这与钢盘表面转移膜的逐渐形成有关。与环块式摩擦磨损测试类似,P/i-PTFE/PS5-S15复合材料在高PV下的摩擦系数和磨损率在整个研究系统中最低。图9提供了对磨钢盘在测试后的光学图像,P/i-PTFE/PS5-S15在滑动界面所形成的转移膜更加均匀,这表明添加不同长径比CFs对复合材料的自润滑性能具有协同改善的效果,另外,复合材料导热性能和机械性能的提升也能改善材料在高PV下的摩擦学性能。Figures 8(A) and (B) show the friction coefficient and wear rate of each resin-based composite material evaluated using a homemade pin-on-disk friction and wear test device, respectively. The duration of the tribological performance test under high PV is 210s, divided into five test cycles, each cycle lasting 42s. As shown in Figure 8(A), the friction coefficients of all samples under high PV decreased with the increase of the test period, which is related to the gradual formation of the transfer film on the surface of the steel disk. Similar to the ring-block friction and wear test, the friction coefficient and wear rate of the P/i-PTFE/PS5-S15 composite under high PV are the lowest in the entire research system. Figure 9 provides the optical image of the counter-grinding steel disc after testing. The transfer film formed by P/i-PTFE/PS5-S15 at the sliding interface is more uniform, which shows that adding CFs with different aspect ratios has a positive effect on the self-lubricating properties of the composite material. It has a synergistic improvement effect. In addition, the improvement of thermal conductivity and mechanical properties of composite materials can also improve the tribological properties of materials under high PV.

综上,本发明的高强度低摩擦耐磨树脂基复合材料同时具有优异的机械强度、导热性能及耐磨损性能,在航空航天、交通运输、电子器件及高端机械装备等领域具有广阔的应用前景。In summary, the high-strength, low-friction and wear-resistant resin-based composite material of the present invention simultaneously has excellent mechanical strength, thermal conductivity and wear resistance, and has broad applications in aerospace, transportation, electronic devices, high-end mechanical equipment and other fields. prospect.

Claims (9)

1. The high-strength low-friction wear-resistant resin matrix composite is characterized by being prepared from the following raw materials in parts by weight: 10-200 parts of resin matrix, 5-80 parts of solid lubricant and 1-60 parts of carbon fiber; the carbon fiber comprises a carbon fiber A and a carbon fiber B, wherein the average length of the carbon fiber A is 0.1-3mm, the average diameter of the carbon fiber A is 1-20 mu m, the average length of the carbon fiber B is 1-20mm, and the average diameter of the carbon fiber B is 1-20 mu m.
2. The high-strength low-friction wear-resistant resin-based composite material according to claim 1, which is characterized by being prepared from the following raw materials in parts by weight: 20-100 parts of resin matrix, 10-50 parts of solid lubricant and 10-40 parts of carbon fiber; the carbon fiber consists of carbon fiber A and carbon fiber B, wherein the weight ratio of the carbon fiber A to the carbon fiber B is (1-3): 1-3.
3. The high-strength low-friction wear-resistant resin-based composite material according to claim 2, which is characterized by being prepared from the following raw materials in parts by weight: 56 parts of a resin matrix, 24 parts of a solid lubricant and 20 parts of carbon fibers; the carbon fiber consists of carbon fiber A and carbon fiber B, wherein the weight ratio of the carbon fiber A to the carbon fiber B is 1:3.
4. The high-strength low-friction wear-resistant resin-based composite material according to claim 1, wherein the carbon fibers a have an average length of 0.2 to 1mm, an average diameter of 2 to 10 μm, and the carbon fibers B have an average length of 2 to 10mm and an average diameter of 2 to 10 μm.
5. The high strength, low friction, wear resistant resin based composite material according to claim 4, wherein the carbon fibers a have an average length of 0.3mm, an average diameter of 6 μm, and the carbon fibers B have an average length of 3mm and an average diameter of 7 μm.
6. The high strength, low friction, wear resistant resin matrix composite according to any one of claims 1 to 5, wherein the resin matrix is a thermoplastic resin, the solid lubricant is polytetrafluoroethylene or a derivative thereof, and the carbon fibers are polyacrylonitrile-based or pitch-based chopped carbon fibers.
7. The high strength, low friction, wear resistant resin matrix composite of claim 6 wherein said resin matrix is polyphenylene sulfide, said derivative of polytetrafluoroethylene is radiation modified polytetrafluoroethylene, and said carbon fibers are polyacrylonitrile-based chopped carbon fibers.
8. A method of preparing the high strength low friction, wear resistant resin based composite material according to any one of claims 1 to 7, said method comprising the steps of: and drying, premixing, and melt blending the raw materials to obtain the product.
9. Use of the high strength low friction wear resistant resin based composite material according to any one of claims 1-8 in the field of aerospace, transportation, electronics and high end mechanical equipment.
CN202410016434.4A 2024-01-04 2024-01-04 A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use Pending CN117757263A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202410016434.4A CN117757263A (en) 2024-01-04 2024-01-04 A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202410016434.4A CN117757263A (en) 2024-01-04 2024-01-04 A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use

Publications (1)

Publication Number Publication Date
CN117757263A true CN117757263A (en) 2024-03-26

Family

ID=90320272

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202410016434.4A Pending CN117757263A (en) 2024-01-04 2024-01-04 A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use

Country Status (1)

Country Link
CN (1) CN117757263A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN118726957A (en) * 2024-09-04 2024-10-01 上海睿岐机械科技有限公司 A self-lubricating composite ceramic coating and its preparation process

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN118726957A (en) * 2024-09-04 2024-10-01 上海睿岐机械科技有限公司 A self-lubricating composite ceramic coating and its preparation process

Similar Documents

Publication Publication Date Title
Kumar et al. Performance of polyimide and PTFE based composites under sliding, erosive and high stress abrasive conditions
Tian et al. Friction behaviors and wear mechanisms of multi-filler reinforced epoxy composites under dry and wet conditions: Effects of loads, sliding speeds, temperatures, water lubrication
Sudheer et al. Enhanced mechanical and wear performance of epoxy/glass composites with PTW/graphite hybrid fillers
Xian et al. Friction and wear of epoxy/TiO2 nanocomposites: Influence of additional short carbon fibers, Aramid and PTFE particles
Liu et al. Effect of hexagonal boron nitride on high-performance polyether ether ketone composites
Wang et al. Study on the friction and wear behavior of basalt fabric composites filled with graphite and nano-SiO2
Wang et al. Optimal analysis for thermal conductivity variation of EVA/SCF composites prepared by spatial confining forced network assembly
CN117757263A (en) A high-strength, low-friction and wear-resistant resin-based composite material and its preparation method and use
Zhao et al. Comparative study on the tribological properties of the polyimide composites reinforced with different fibers
Meng et al. The influence of several silicates on the fretting behavior of UHMWPE composites
JPS58160346A (en) Resin composition
Su et al. Study on the tribological properties of carbon fabric/polyimide composites filled with SiC nanoparticles
Chen et al. Tribological behavior of carbon-fiber-reinforced polymer with highly oriented graphite nanoplatelets
Lv et al. An investigation of the microstructure and tribological behavior of polyether ether ketone composites fabricated by extrusion‐based additive manufacturing
Zhang et al. Effects of carbon fibers with different particle sizes on the physical properties of MoS2-filled PTFE composites
Lv et al. Tribological anisotropy of PEEK composites filled with highly oriented carbon fibers manufactured by fused deposition modeling
Lv et al. Tribological behavior of PEEK based composites with alternating layered structure fabricated via fused deposition modeling
CN115785671A (en) A kind of airgel/polyphenylene sulfide self-lubricating friction material and preparation method thereof
Song et al. Effect of surface roughness and reciprocating time on the tribological properties of the polyimide composites
Chauhan et al. Synergistic effects of micro size flyash particulate and glass fiber on friction and wear of vinylester hybrid composites under dry and water lubricated sliding condition
Midan et al. Effect of carbon fiber content on mechanical and tribological properties of carbon/phenolic resin composites
Sahin et al. TRIBOLOGICAL BEHAVIOUR OF BASALT FABRIC-REINFORCED EPOXY COMPOSITES.
CN113337130B (en) A kind of isolation network composite material containing hybrid nanofiller, its preparation method and use
CN109825014A (en) A kind of high elastic modulus polytetrafluoroethylene friction material and its preparation method and application
NP Friction and Wear Characteristics of Additive Manufactured CNT-Reinforced HDPE Composites in Dry Contact.

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination