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 PDFInfo
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- 229920006130 high-performance polyamide Polymers 0.000 title claims abstract description 13
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- 239000002783 friction material Substances 0.000 title abstract description 13
- 229920002292 Nylon 6 Polymers 0.000 claims abstract description 23
- 239000000463 material Substances 0.000 claims abstract description 23
- 239000003365 glass fiber Substances 0.000 claims abstract description 20
- 239000002131 composite material Substances 0.000 claims abstract description 19
- 239000000314 lubricant Substances 0.000 claims abstract description 18
- 239000007787 solid Substances 0.000 claims abstract description 17
- 239000003063 flame retardant Substances 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 230000003712 anti-aging effect Effects 0.000 claims abstract description 9
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 8
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 22
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical group CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 claims description 7
- 150000003973 alkyl amines Chemical class 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 6
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims 6
- 229920010741 Ultra High Molecular Weight Polyethylene (UHMWPE) Polymers 0.000 claims 4
- 239000003112 inhibitor Substances 0.000 claims 4
- 230000003068 static effect Effects 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 238000005453 pelletization Methods 0.000 claims 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 12
- 238000002156 mixing Methods 0.000 abstract description 9
- 239000002216 antistatic agent Substances 0.000 abstract description 8
- 230000007797 corrosion Effects 0.000 abstract description 4
- 238000005260 corrosion Methods 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 230000032683 aging Effects 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 238000002844 melting Methods 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 14
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 14
- -1 polytetrafluoroethylene Polymers 0.000 description 13
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 7
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 4
- 239000010439 graphite Substances 0.000 description 4
- 229910002804 graphite Inorganic materials 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 2
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000012757 flame retardant agent Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920002530 polyetherether ketone Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YMIUHIAWWDYGGU-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-[2,3,5,6-tetrabromo-4-(2,3,4,5,6-pentabromophenoxy)phenoxy]benzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC(C(=C1Br)Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br YMIUHIAWWDYGGU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000013386 optimize process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/04—Antistatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/06—Properties of polyethylene
- C08L2207/068—Ultra high molecular weight polyethylene
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- 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
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.
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