[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN105385151A - High performance polyamide 6 based friction material and preparation method thereof - Google Patents

High performance polyamide 6 based friction material and preparation method thereof Download PDF

Info

Publication number
CN105385151A
CN105385151A CN201510895557.0A CN201510895557A CN105385151A CN 105385151 A CN105385151 A CN 105385151A CN 201510895557 A CN201510895557 A CN 201510895557A CN 105385151 A CN105385151 A CN 105385151A
Authority
CN
China
Prior art keywords
weight
polyamide
mass ratio
agent
tetrafluoroethylene
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
CN201510895557.0A
Other languages
Chinese (zh)
Inventor
李笃信
游一兰
司高杰
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.)
Central South University
Original Assignee
Central South 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 Central South University filed Critical Central South University
Priority to CN201510895557.0A priority Critical patent/CN105385151A/en
Publication of CN105385151A publication Critical patent/CN105385151A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/02Flame or fire retardant/resistant
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/04Antistatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2207/00Properties characterising the ingredient of the composition
    • C08L2207/06Properties of polyethylene
    • C08L2207/068Ultra high molecular weight polyethylene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种高性能聚酰胺6基摩擦材料及其制备方法,该摩擦材料按质量分数组成包括:聚酰胺6:55%~65%,短切玻璃纤维:10%~15%,复合固体润滑剂:10%~15%,增容剂:2%~5%,阻燃剂:10%~15%,抗静电剂:0.5%~2%,抗老化剂:0.05%~0.5%,硅烷偶联剂:0.5%~1%;将所有材料按质量配比混匀后,采用熔融法制得高性能聚酰胺6基摩擦材料。该摩擦材料具有制作工艺简单、磨损率低、摩擦系数低、强度高、阻燃、抗静电、耐高低温、抗腐蚀、抗老化、成本低等优点。The invention discloses a high-performance polyamide 6-based friction material and a preparation method thereof. The friction material comprises: polyamide 6: 55% to 65%, chopped glass fiber: 10% to 15%, and composite Solid lubricant: 10% to 15%, compatibilizer: 2% to 5%, flame retardant: 10% to 15%, antistatic agent: 0.5% to 2%, antiaging agent: 0.05% to 0.5%, Silane coupling agent: 0.5% to 1%; after mixing all the materials according to the mass ratio, the high-performance polyamide 6-based friction material is prepared by melting method. The friction material has the advantages of simple manufacturing process, low wear rate, low friction coefficient, high strength, flame retardancy, antistatic, high and low temperature resistance, corrosion resistance, aging resistance, and low cost.

Description

一种高性能聚酰胺6基摩擦材料及其制备方法A high-performance polyamide 6-based friction material and its preparation method

技术领域technical field

本发明涉及一种高分子材料改性领域,尤其涉及一种高性能聚酰胺6基摩擦材料及其制备方法。The invention relates to the field of polymer material modification, in particular to a high-performance polyamide 6-based friction material and a preparation method thereof.

背景技术Background technique

聚酰胺6具有力学强度高、韧性佳、电气性能优良、抗震吸音、耐弱酸弱碱及一些有机溶剂,自润滑性能优异,易于成型加工等特性,工业生产中广泛应用于制造轴承、齿轮、凸轮、各种滚子、滑轮等摩擦器件。但其尺寸稳定性差,吸水率大,干摩擦时摩擦系数较高,热、力学性能还不足以应付高速摩擦等缺点,使其应用仍受到一定的限制。Polyamide 6 has the characteristics of high mechanical strength, good toughness, excellent electrical properties, shock resistance and sound absorption, resistance to weak acids and bases and some organic solvents, excellent self-lubricating properties, and easy molding and processing. It is widely used in the manufacture of bearings, gears, and cams in industrial production. , Various rollers, pulleys and other friction components. However, its poor dimensional stability, high water absorption, high friction coefficient during dry friction, thermal and mechanical properties are not enough to cope with high-speed friction and other shortcomings, so its application is still limited.

近年来,国内外通过添加纤维、无机粒子提高聚酰胺6的耐磨性和力学性能却往往增大了摩擦系数;而通过添加固体润滑剂,可降低摩擦系数,却可能增大了磨损率、降低了其力学性能;添加阻燃、抗静电剂制得阻燃抗静电复合材料的同时,力学性能和摩擦磨损性能降低,高强度、阻燃、耐磨聚酰胺6复合材料的制备亟待解决。In recent years, the addition of fibers and inorganic particles to improve the wear resistance and mechanical properties of polyamide 6 at home and abroad often increases the friction coefficient; while the addition of solid lubricants can reduce the friction coefficient, but may increase the wear rate, Reduce its mechanical properties; add flame retardant, antistatic agent to prepare flame retardant antistatic composite material, mechanical properties and friction and wear properties decrease, high strength, flame retardant, wear-resistant polyamide 6 composite material preparation urgently needs to be solved.

专利CN103102A介绍了一种高抗冲击阻燃耐磨聚酰胺6复合材料的制备方法,得到较高冲击强度及氧指数的聚酰胺6复合材料,但其摩擦系数及磨耗仍较大。Patent CN103102A introduces a preparation method of a high-impact, flame-retardant and wear-resistant polyamide 6 composite material, and obtains a polyamide 6 composite material with high impact strength and oxygen index, but its friction coefficient and wear are still relatively large.

针对这种情况,本发明创新性的在聚酰胺6基体中加入玻璃纤维和复合固体润滑剂,发挥其协同效应,配以阻燃剂和抗静电剂,制备出一种磨损率低、摩擦系数低、强度高、阻燃、抗静电的高性能聚酰胺6基摩擦材料,具有非常重要的现实意义。In response to this situation, the present invention innovatively adds glass fiber and composite solid lubricant to the polyamide 6 matrix to exert its synergistic effect, and prepares a kind of lubricant with low wear rate and low friction coefficient with the addition of flame retardant and antistatic agent. The high-performance polyamide 6-based friction material with low weight, high strength, flame retardancy and antistatic has very important practical significance.

发明内容Contents of the invention

本发明的目的是提供一种磨损率低、摩擦系数低、强度高、阻燃、抗静电、耐高低温、抗腐蚀、抗老化的高性能聚酰胺6基摩擦材料。The purpose of the present invention is to provide a high-performance polyamide 6-based friction material with low wear rate, low friction coefficient, high strength, flame retardancy, antistatic, high and low temperature resistance, corrosion resistance and aging resistance.

为了达到上述目的,本发明包括:聚酰胺6树脂:55~65%(重量),短切玻璃纤维:10~15%(重量),复合固体润滑剂:10~15%(重量),增容剂:3~5%(重量),阻燃剂:10~15%(重量),抗静电剂:0.5~2%(重量),抗老化剂:0.05~0.5%(重量),硅烷偶联剂:0.5~1%(重量),其中复合固体润滑剂粒径为5~10μm,由质量比为1∶1~2∶1的聚四氟乙烯、超高分子量聚乙烯组成或者由质量比为1∶1~2∶1聚四氟乙烯、石墨粉组成或者由质量比为1∶1∶1的聚四氟乙烯、超高分子量聚乙烯、石墨粉组成;所述的增容剂为HDPE-g-MAH或POE-g-MAH;所述的阻燃剂为质量比为1∶3~1∶4的三氧化二锑、十四溴二苯氧基苯或者质量比为1∶3~1∶4的三氧化二锑、十溴二苯醚;所述的抗静电剂为乙氧基化烷基胺;所述的抗老化剂为抗氧剂1010。In order to achieve the above object, the present invention includes: polyamide 6 resin: 55-65% (weight), chopped glass fiber: 10-15% (weight), composite solid lubricant: 10-15% (weight), compatibilization Agent: 3-5% (weight), flame retardant: 10-15% (weight), antistatic agent: 0.5-2% (weight), anti-aging agent: 0.05-0.5% (weight), silane coupling agent : 0.5-1% (weight), wherein the particle size of the composite solid lubricant is 5-10 μm, composed of polytetrafluoroethylene and ultra-high molecular weight polyethylene with a mass ratio of 1:1-2:1 or composed of polytetrafluoroethylene and ultra-high molecular weight polyethylene with a mass ratio of 1 : 1 to 2: 1 polytetrafluoroethylene, graphite powder or composed of polytetrafluoroethylene, ultra-high molecular weight polyethylene, graphite powder with a mass ratio of 1: 1: 1; the compatibilizer is HDPE-g -MAH or POE-g-MAH; the flame retardant is antimony trioxide and tetradetrabromodiphenoxybenzene with a mass ratio of 1:3 to 1:4 or a mass ratio of 1:3 to 1: Antimony trioxide and decabromodiphenyl ether in 4; the antistatic agent is ethoxylated alkylamine; the antiaging agent is antioxidant 1010.

优选的,所述的聚酰胺6树脂的相对粘度为2.80~2.95。Preferably, the relative viscosity of the polyamide 6 resin is 2.80-2.95.

优选的,所述的短切玻璃纤维为长度3~5mm的E玻璃纤维。Preferably, the chopped glass fibers are E glass fibers with a length of 3-5 mm.

本发明的另一个目的为提供一种高性能聚酰胺6基摩擦材料的制备方法,包括:1)按聚酰胺6树脂:55~65%(重量),短切玻璃纤维:10~15%(重量),复合固体润滑剂:10~15%(重量),增容剂:3~5%(重量),阻燃剂:10~15%(重量),抗静电剂:0.5~2%(重量),抗老化剂:0.05~0.5%(重量),硅烷偶联剂:0.5~1%(重量)配料,其中复合固体润滑剂粒径为5~10μm,由质量比为1∶1~2∶1的聚四氟乙烯、超高分子量聚乙烯组成或者由质量比为1∶1~2∶1聚四氟乙烯、石墨粉组成或者由质量比为1∶1∶1的聚四氟乙烯、超高分子量聚乙烯、石墨粉组成;所述的增容剂为HDPE-g-MAH或POE-g-MAH;所述的阻燃剂为质量比为1∶3~1∶4的三氧化二锑、十四溴二苯氧基苯或者质量比为1∶3~1∶4的三氧化二锑、十溴二苯醚;所述的抗静电剂为乙氧基化烷基胺;所述的抗老化剂为抗氧剂1010;2)混合均匀;3)在190~250℃挤出造粒;4)干燥除去水分。Another object of the present invention is to provide a kind of preparation method of high-performance polyamide 6 base friction material, comprising: 1) by polyamide 6 resin: 55~65% (weight), chopped glass fiber: 10~15% ( weight), composite solid lubricant: 10-15% (weight), compatibilizer: 3-5% (weight), flame retardant: 10-15% (weight), antistatic agent: 0.5-2% (weight ), anti-aging agent: 0.05~0.5% (weight), silane coupling agent: 0.5~1% (weight) ingredients, wherein the particle size of the composite solid lubricant is 5~10 μm, and the mass ratio is 1:1~2: 1 of polytetrafluoroethylene and ultra-high molecular weight polyethylene or composed of polytetrafluoroethylene and graphite powder with a mass ratio of 1:1 to 2:1 or composed of polytetrafluoroethylene and ultra-high molecular weight polyethylene with a mass ratio of 1:1:1 Composed of high molecular weight polyethylene and graphite powder; the compatibilizer is HDPE-g-MAH or POE-g-MAH; the flame retardant is antimony trioxide with a mass ratio of 1:3 to 1:4 , Tetrabromodiphenoxybenzene or antimony trioxide and decabromodiphenyl ether with a mass ratio of 1:3 to 1:4; the antistatic agent is ethoxylated alkylamine; the The anti-aging agent is antioxidant 1010; 2) mixing uniformly; 3) extruding and granulating at 190-250° C.; 4) drying to remove water.

优选的,所述的聚酰胺6树脂的相对粘度为2.80~2.95。Preferably, the relative viscosity of the polyamide 6 resin is 2.80-2.95.

优选的,所述的短切玻璃纤维为长度3~5mm的E玻璃纤维。Preferably, the chopped glass fibers are E glass fibers with a length of 3-5 mm.

本发明选用具有良好的耐磨性、韧性、机械强度且价格相对便宜、易于成型的聚酰胺6为基体材料,克服了采用聚四氟乙烯(PTFE)、聚酰亚胺(PI)、聚醚醚酮(PEEK)、聚苯硫醚(PPS)等为基材时成型条件苛刻、价格高的缺点。玻璃纤维具有很高的强度和刚度、良好的导热性、小的伸长率和热膨胀系数,并能耐许多介质的腐蚀,不燃烧,在低于250℃的环境下耐温性能好,所以采用玻纤增强聚酰胺6,可以获得力学性能、耐磨性、耐热性好的摩擦材料,延长制品的使用寿命。固体润滑剂因在摩擦过程中在接触界面上形成了低剪切强度的转移膜而具有抗磨减摩的效果;选用复合固体润滑剂不仅可起到润滑的作用,还能有效防止玻璃纤维外露,从而大大改善了材料的摩擦磨损性能。该摩擦材料中纤维起增强作用保证力学性能并提高耐磨性、和热稳定性;由于复合固体润滑剂降低摩擦系数,从而提高了聚酰胺6的使用性能。本发明具有生产工序简单、成本低、在获得优异的摩擦磨损、阻燃、抗静电以及热性能的同时,保持了材料优异的力学性能的优点。所用复合固体润滑剂与单一固体润滑剂相比具有协同作用,制备出的材料同时具有更低的摩擦系数和磨损率。聚四氟乙烯显著降低材料的摩擦系数,石墨降低摩擦系数的同时,增大了材料导热率,使摩擦热快速导出,减缓了材料在摩擦过程中的熔融,同时降低了材料的表面电阻,超高分子量聚乙烯、聚四氟乙烯和石墨共同使用时具有显著的协同效应,三者协同改性的聚酰胺6复合材料较单一固体润滑剂填充改性的复合材料具有更低的摩擦系数和磨损率,在此基础上添加优选的阻燃剂和抗静电剂,得到一种磨损率低、摩擦系数低、强度高、阻燃、抗静电、耐高低温、抗腐蚀、抗老化的高性能聚酰胺6基摩擦材料。对于合适配方在优化工艺下制备的材料进行分析和评估,得到如下基本性能。轴向拉伸强度≥60MPa,缺口冲击强度≥25KJ/m2,使用温度-30~150℃,密度≥1.62g/cm3,阻燃性能:V-0,表面电阻<5×108Ω;摩擦系数:0.02~0.13,磨损率4.5×10-6~3.31×10-5mm3/Nm。本发明的聚酰胺6基摩擦材料具有高性能的特点,应用范围广,具有广阔的市场前景。The present invention selects the polyamide 6 that has good wear resistance, toughness, mechanical strength and relatively cheap price, and is easy to shape as the matrix material, overcomes the need to adopt polytetrafluoroethylene (PTFE), polyimide (PI), polyether Ether ketone (PEEK), polyphenylene sulfide (PPS), etc. are the disadvantages of harsh molding conditions and high prices when used as base materials. Glass fiber has high strength and rigidity, good thermal conductivity, small elongation and thermal expansion coefficient, and can withstand the corrosion of many media, does not burn, and has good temperature resistance in an environment below 250 ° C, so glass fiber is used Fiber-reinforced polyamide 6 can obtain friction materials with good mechanical properties, wear resistance and heat resistance, and prolong the service life of products. The solid lubricant has the effect of anti-wear and anti-friction due to the formation of a low-shear strength transfer film on the contact interface during the friction process; the selection of a composite solid lubricant can not only play the role of lubrication, but also effectively prevent the glass fiber from being exposed , thereby greatly improving the friction and wear properties of the material. The fiber in the friction material acts as a reinforcement to ensure mechanical properties and improve wear resistance and thermal stability; since the composite solid lubricant reduces the friction coefficient, the performance of the polyamide 6 is improved. The invention has the advantages of simple production process, low cost, excellent friction and wear, flame retardancy, antistatic and thermal properties, and maintains the excellent mechanical properties of the material. Compared with the single solid lubricant, the composite solid lubricant has a synergistic effect, and the prepared material has lower friction coefficient and wear rate at the same time. PTFE significantly reduces the friction coefficient of the material. While graphite reduces the friction coefficient, it increases the thermal conductivity of the material, so that the friction heat can be quickly exported, slowing down the melting of the material during the friction process, and at the same time reducing the surface resistance of the material. When high molecular weight polyethylene, polytetrafluoroethylene and graphite are used together, there is a significant synergistic effect. The polyamide 6 composite material modified by the three synergistically has a lower friction coefficient and wear than the composite material modified by a single solid lubricant On this basis, the preferred flame retardant and antistatic agent are added to obtain a high-performance polymer with low wear rate, low friction coefficient, high strength, flame retardancy, antistatic, high and low temperature resistance, corrosion resistance and aging resistance. Amide 6 based friction material. The following basic properties are obtained by analyzing and evaluating the materials prepared under the optimized process with a suitable formula. Axial tensile strength ≥60MPa, notched impact strength ≥25KJ/m 2 , service temperature -30~150°C, density ≥1.62g/cm 3 , flame retardant performance: V-0, surface resistance <5×10 8 Ω; Friction coefficient: 0.02~0.13, wear rate 4.5×10 -6 ~3.31×10 -5 mm 3 /Nm. The polyamide 6-based friction material of the invention has the characteristics of high performance, wide application range and broad market prospect.

具体实施方式:detailed description:

下面举实例对本发明进行详细描述,而不是限制发明的范围。The following examples are given to describe the present invention in detail, but not to limit the scope of the invention.

实施例1Example 1

1)按聚酰胺6树脂:55%(重量),3~5mm的E玻璃纤维:15%(重量),聚四氟乙烯:7%(重量)、POE-g-MAH:3.5%(重量);石墨:3.5%(重量),十溴二苯醚:10%(重量),三氧化二锑:3%(重量),乙氧基化烷基胺:2%(重量),抗氧剂1010:0.5%(重量),硅烷偶联剂:0.5%(重量)配料;2)高速混合0.5小时,转速为300~600转/分混合均匀;3)双螺杆挤出机的温度控制在190~250℃混炼挤出,水冷经切粒机切成规格为Φ2.5×4的粒料;4)在100℃干燥3小时。1) According to polyamide 6 resin: 55% (weight), 3-5mm E glass fiber: 15% (weight), polytetrafluoroethylene: 7% (weight), POE-g-MAH: 3.5% (weight) ;Graphite: 3.5% by weight, decabromodiphenyl ether: 10% by weight, antimony trioxide: 3% by weight, ethoxylated alkylamine: 2% by weight, antioxidant 1010 : 0.5% (weight), silane coupling agent: 0.5% (weight) batching; 2) high-speed mixing for 0.5 hours, rotating speed is 300~600 rev/min mixing; 3) the temperature of the twin-screw extruder is controlled at 190~ Mix and extrude at 250°C, water-cool and cut into pellets with a specification of Φ2.5×4 through a pelletizer; 4) Dry at 100°C for 3 hours.

对于该配方的材料进行分析和评估,得到如下基本性能。轴向拉伸强度:67MPa,缺口冲击强度:27.7KJ/m2,阻燃性能:V-0,表面电阻:4.2×108Ω;摩擦系数:0.08,磨损率:5.5×10-6mm3/Nm。The materials of this formula are analyzed and evaluated, and the following basic properties are obtained. Axial tensile strength: 67MPa, notched impact strength: 27.7KJ/m 2 , flame retardancy: V-0, surface resistance: 4.2×10 8 Ω; friction coefficient: 0.08, wear rate: 5.5×10 -6 mm 3 /Nm.

实施例2Example 2

1)按聚酰胺6树脂:58%(重量),3~5mm的E玻璃纤维:12.5%(重量),聚四氟乙烯:6%(重量)、HDPE-g-MAH:3.5%(重量);超高分子量聚乙烯:3%(重量),十溴二苯醚:11%(重量),三氧化二锑:3.5%(重量),乙氧基化烷基胺:1.5%(重量),抗氧剂1010:0.5%(重量),硅烷偶联剂:0.5%(重量)配料;2)高速混合0.5小时,转速为300~600转/分混合均匀;3)双螺杆挤出机的温度控制在190~250℃混炼挤出,水冷经切粒机切成规格为Φ2.5×4的粒料;4)在100℃干燥3小时。1) According to polyamide 6 resin: 58% (weight), E glass fiber of 3 ~ 5mm: 12.5% (weight), polytetrafluoroethylene: 6% (weight), HDPE-g-MAH: 3.5% (weight) ; UHMWPE: 3% by weight, Decabromodiphenyl ether: 11% by weight, Antimony trioxide: 3.5% by weight, Ethoxylated alkylamine: 1.5% by weight, Antioxidant 1010: 0.5% (weight), silane coupling agent: 0.5% (weight) batching; 2) high-speed mixing for 0.5 hours, and the rotating speed is 300~600 rpm to mix evenly; 3) the temperature of the twin-screw extruder Mixing and extrusion controlled at 190-250°C, water-cooled and cut into pellets with a specification of Φ2.5×4 by a pelletizer; 4) Drying at 100°C for 3 hours.

对于该配方的材料进行分析和评估,得到如下基本性能。轴向拉伸强度:65.3MPa,缺口冲击强度:25.8KJ/m2,阻燃性能:V-0,表面电阻:4.4×108Ω;摩擦系数:0.1,磨损率:4.5×10-6mm3/Nm。The materials of this formula are analyzed and evaluated, and the following basic properties are obtained. Axial tensile strength: 65.3MPa, notched impact strength: 25.8KJ/m 2 , flame retardancy: V-0, surface resistance: 4.4×10 8 Ω; friction coefficient: 0.1, wear rate: 4.5×10 -6 mm 3 /Nm.

实施例3Example 3

1)按聚酰胺6树脂:65%(重量),3~5mm的E玻璃纤维:10%(重量),聚四氟乙烯:3.5%(重量),HDPE-g-MAH:2%(重量),超高分子量聚乙烯:3.5%(重量),石墨:3.5%(重量),十四溴二苯氧基苯:8.5%(重量),三氧化二锑:2.5%(重量),乙氧基化烷基胺:0.8%(重量),抗氧剂1010:0.2%(重量),硅烷偶联剂:0.5%(重量)配料;2)高速混合0.5小时,转速为300~600转/分混合均匀;3)双螺杆挤出机的温度控制在190~250℃混炼挤出,水冷经切粒机切成规格为Φ2.5×4的粒料;4)在100℃干燥3小时。1) According to polyamide 6 resin: 65% (weight), E glass fiber of 3 ~ 5mm: 10% (weight), polytetrafluoroethylene: 3.5% (weight), HDPE-g-MAH: 2% (weight) , ultra-high molecular weight polyethylene: 3.5% (weight), graphite: 3.5% (weight), tetradecabromodiphenoxybenzene: 8.5% (weight), antimony trioxide: 2.5% (weight), ethoxy Alkylamine: 0.8% (weight), antioxidant 1010: 0.2% (weight), silane coupling agent: 0.5% (weight) ingredients; 2) high-speed mixing for 0.5 hours, rotating speed is 300~600 rev/min mixing Uniform; 3) The temperature of the twin-screw extruder is controlled at 190-250°C for mixing and extrusion, water-cooled and cut into pellets with a specification of Φ2.5×4 by a pelletizer; 4) Drying at 100°C for 3 hours.

对于该配方的材料进行分析和评估,得到如下基本性能。轴向拉伸强度:63.5MPa,缺口冲击强度:27.8KJ/m2,阻燃性能:V-0,表面电阻:4.0×108Ω;摩擦系数:0.05,磨损率:3.3×10-6mm3/Nm。The materials of this formula are analyzed and evaluated, and the following basic properties are obtained. Axial tensile strength: 63.5MPa, notched impact strength: 27.8KJ/m 2 , flame retardancy: V-0, surface resistance: 4.0×10 8 Ω; friction coefficient: 0.05, wear rate: 3.3×10 -6 mm 3 /Nm.

Claims (6)

1. a high-performance polyamide 6 base frication material, it is characterized in that, comprise: polyamide 6: 55 ~ 65% (weight), short glass fiber: 10 ~ 15% (weight), composite solid lubricating agent: 10 ~ 15% (weight), expanding material: 3 ~ 5% (weight), fire retardant: 10 ~ 15% (weight), static inhibitor: 0.5 ~ 2% (weight), antiaging agent: 0.05 ~ 0.5% (weight), silane coupling agent: 0.5 ~ 1% (weight), wherein composite solid lubricating agent particle diameter is 5 ~ 10 μm, be the tetrafluoroethylene of 1: 1 ~ 2: 1 by mass ratio, ultrahigh molecular weight polyethylene(UHMWPE) forms or is 1: 1 ~ 2: 1 tetrafluoroethylene by mass ratio, Graphite Powder 99 forms or is the tetrafluoroethylene of 1: 1: 1 by mass ratio, ultrahigh molecular weight polyethylene(UHMWPE), Graphite Powder 99 forms, described expanding material is HDPE-g-MAH or POE-g-MAH, described fire retardant to be mass ratio be 1: 3 ~ 1: 4 antimonous oxide, ten tetrabromo two phenoxy group benzene or mass ratio be 1: 3 ~ 1: 4 antimonous oxide, decabromodiphynly oxide, described static inhibitor is ethoxylated alkylamine, described antiaging agent is antioxidant 1010.
2. a kind of high-performance polyamide 6 base frication material according to claim 1, is characterized in that, the relative viscosity of described polyamide 6 is 2.80 ~ 2.95.
3. a kind of high-performance polyamide 6 base frication material according to claim 1, is characterized in that, described short glass fiber is the E glass fibre of length 3 ~ 5mm.
4. the preparation method of a high-performance polyamide 6 base frication material, it is characterized in that, comprise: 1) by polyamide 6: 55 ~ 65% (weight), short glass fiber: 10 ~ 15% (weight), composite solid lubricating agent: 10 ~ 15% (weight), expanding material: 3 ~ 5% (weight), fire retardant: 10 ~ 15% (weight), static inhibitor: 0.5 ~ 2% (weight), antiaging agent: 0.05 ~ 0.5% (weight), silane coupling agent: 0.5 ~ 1% (weight) prepares burden, wherein composite solid lubricating agent particle diameter is 5 ~ 10 μm, be the tetrafluoroethylene of 1: 1 ~ 2: 1 by mass ratio, ultrahigh molecular weight polyethylene(UHMWPE) forms or is 1: 1 ~ 2: 1 tetrafluoroethylene by mass ratio, Graphite Powder 99 forms or is the tetrafluoroethylene of 1: 1: 1 by mass ratio, ultrahigh molecular weight polyethylene(UHMWPE), Graphite Powder 99 forms, described expanding material is HDPE-g-MAH or POE-g-MAH, described fire retardant to be mass ratio be 1: 3 ~ 1: 4 antimonous oxide, ten tetrabromo two phenoxy group benzene or mass ratio be 1: 3 ~ 1: 4 antimonous oxide, decabromodiphynly oxide, described static inhibitor is ethoxylated alkylamine, described antiaging agent is antioxidant 1010, 2) mix, 3) at 190 ~ 250 DEG C of extruding pelletizations, 4) dry removing moisture.
5. the preparation method of a kind of high-performance polyamide 6 base frication material according to claim 4, is characterized in that, the relative viscosity of described polyamide 6 is 2.80 ~ 2.95.
6. the preparation method of a kind of high-performance polyamide 6 base frication material according to claim 4, is characterized in that, described short glass fiber is the E glass fibre of length 3 ~ 5mm.
CN201510895557.0A 2015-12-04 2015-12-04 High performance polyamide 6 based friction material and preparation method thereof Pending CN105385151A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510895557.0A CN105385151A (en) 2015-12-04 2015-12-04 High performance polyamide 6 based friction material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510895557.0A CN105385151A (en) 2015-12-04 2015-12-04 High performance polyamide 6 based friction material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN105385151A true CN105385151A (en) 2016-03-09

Family

ID=55417951

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510895557.0A Pending CN105385151A (en) 2015-12-04 2015-12-04 High performance polyamide 6 based friction material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105385151A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107053792A (en) * 2017-06-12 2017-08-18 济南天齐特种平带有限公司 A kind of high-performance hangs band
CN108440954A (en) * 2018-03-15 2018-08-24 湖南格林美映鸿资源循环有限公司 A kind of PA6 based composites and preparation method thereof
CN108690697A (en) * 2018-06-25 2018-10-23 重庆聚洋无油轴承有限公司 A kind of kollag and preparation method thereof
CN112608593A (en) * 2020-11-16 2021-04-06 天津渤化永利化工股份有限公司 Polyamide 66 ternary alloy anticorrosive resin and preparation method thereof
CN112898767A (en) * 2021-01-25 2021-06-04 江阴市宏丰塑业有限公司 High-temperature-resistant antistatic modified polyamide and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4877813A (en) * 1984-10-22 1989-10-31 Taiho Kogyo Co., Ltd. Bearing resin material
CN1607219A (en) * 2003-10-14 2005-04-20 林安良 High self-lubricating, high wear resisting, reinforced nylon engineering plastic alloy and method for making same
CN101423665A (en) * 2008-12-03 2009-05-06 中南大学 High performance polymer base composite material for support roller and preparation method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4877813A (en) * 1984-10-22 1989-10-31 Taiho Kogyo Co., Ltd. Bearing resin material
CN1607219A (en) * 2003-10-14 2005-04-20 林安良 High self-lubricating, high wear resisting, reinforced nylon engineering plastic alloy and method for making same
CN101423665A (en) * 2008-12-03 2009-05-06 中南大学 High performance polymer base composite material for support roller and preparation method

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
YI-LAN YOU. ET AL: "Effect of Solid Lubricants on Tribological Behavior of Glass Fiber Reinforced Polyamide 6", 《POLYMER COMPOSITES》 *
刘正英 等: "《工程塑料改性技术》", 31 January 2008, 化学工业出版社 *
游一兰: "增强PA6基多相摩擦材料及其摩擦磨损特性研究", 《中国博士学位论文全文数据库 工程科技I辑》 *
王文广 等: "《塑料配方设计》", 31 July 2004, 化学工业出版社 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107053792A (en) * 2017-06-12 2017-08-18 济南天齐特种平带有限公司 A kind of high-performance hangs band
CN108440954A (en) * 2018-03-15 2018-08-24 湖南格林美映鸿资源循环有限公司 A kind of PA6 based composites and preparation method thereof
CN108440954B (en) * 2018-03-15 2020-10-16 湖南格林美映鸿资源循环有限公司 PA 6-based composite material and preparation method thereof
CN108690697A (en) * 2018-06-25 2018-10-23 重庆聚洋无油轴承有限公司 A kind of kollag and preparation method thereof
CN108690697B (en) * 2018-06-25 2021-04-06 重庆聚洋无油轴承有限公司 Solid lubricant and preparation method thereof
CN112608593A (en) * 2020-11-16 2021-04-06 天津渤化永利化工股份有限公司 Polyamide 66 ternary alloy anticorrosive resin and preparation method thereof
CN112898767A (en) * 2021-01-25 2021-06-04 江阴市宏丰塑业有限公司 High-temperature-resistant antistatic modified polyamide and preparation method thereof

Similar Documents

Publication Publication Date Title
CN105385151A (en) High performance polyamide 6 based friction material and preparation method thereof
CN105860524B (en) A kind of thermoplasticity low friction wearing composite material and preparation method thereof
CN103242641B (en) Polyaryletherketone-based abrasion-resistant composite material and preparation method thereof
CN102093716B (en) Polyphenylene sulfide/polyether sulfone-based compound material and preparation method thereof as well as wear-resistant part prepared from polyphenylene sulfide/polyether sulfone-based compound material
CN110078996A (en) Coal mine self-lubricating type hdpe pipe and preparation method thereof
RU2550386C2 (en) Wear-resistant material made of modified polytetrafluoroethylene
CN103087468A (en) Polyether-ether-ketone composite material with high heat resistance and high wear resistance and preparation process thereof
CN101735554A (en) Polyetheretherketone composite material, preparation method and application thereof
CN105062069B (en) Wear-resistant modified polyimide composite material and preparation method thereof
CN108084707B (en) Nylon material for petroleum lining pipe and preparation method thereof
CN104151768A (en) Carbon fiber reinforced ABS (Acrylonitrile Butadiene Styrene) resin composite material with superior heat conductivity and preparation method
CN104177829A (en) Toughened wear-resistant composite material and preparation method thereof
CN1301298C (en) self-lubricating bearing material and preparation method thereof
JP5913976B2 (en) Fluororesin composition and sliding member
CN115785671B (en) Aerogel/polyphenylene sulfide self-lubricating friction material and preparation method thereof
CN106433020B (en) A kind of binary environmental protection polyether-ether-ketone base brake pad material and preparation method thereof
CN101575437B (en) Self-lubricating polyoxymethylene/nano polytetrafluoroethylene blended compound material and preparation method thereof
CN101875777B (en) Polymer-ceramic composite material
CN106675025A (en) Polyimide-modified material and preparation method and application thereof
CN108384229A (en) A kind of composite fibre reinforced nylon 6 reworked material and preparation method thereof
CN103897388B (en) A kind of high-performance lower shrinkage release bearing nylon sleeve material and preparation method
CN105001566A (en) Polytetrafluoroethylene/polyimide composite material and preparation method thereof
CN106090015B (en) A kind of two-stage type plastic sliding bearing with material synergistic effect
CN106867240A (en) A kind of wear-resistant self-lubricating nylon compound material and preparation method thereof
CN103483812B (en) A kind of preparation method of the wear resistant nylon 66 containing antioxidant

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20160309