CN115746551B - High temperature resistant self-lubricating motor bearing holder - Google Patents
High temperature resistant self-lubricating motor bearing holder Download PDFInfo
- Publication number
- CN115746551B CN115746551B CN202211126100.XA CN202211126100A CN115746551B CN 115746551 B CN115746551 B CN 115746551B CN 202211126100 A CN202211126100 A CN 202211126100A CN 115746551 B CN115746551 B CN 115746551B
- Authority
- CN
- China
- Prior art keywords
- stirring
- parts
- temperature
- mesoporous silica
- composite material
- 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.)
- Active
Links
- 239000002131 composite material Substances 0.000 claims abstract description 66
- 239000002071 nanotube Substances 0.000 claims abstract description 57
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 52
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical class O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 claims abstract description 50
- 229920002647 polyamide Polymers 0.000 claims abstract description 42
- 239000011159 matrix material Substances 0.000 claims abstract description 32
- 239000000314 lubricant Substances 0.000 claims abstract description 27
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 26
- 239000003822 epoxy resin Substances 0.000 claims abstract description 21
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 21
- 239000002270 dispersing agent Substances 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 15
- 239000002667 nucleating agent Substances 0.000 claims abstract description 13
- 239000002994 raw material Substances 0.000 claims abstract description 9
- 239000002105 nanoparticle Substances 0.000 claims abstract description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 4
- 238000003756 stirring Methods 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 25
- 229910052621 halloysite Inorganic materials 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 16
- 238000002156 mixing Methods 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 10
- 238000001914 filtration Methods 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 239000007822 coupling agent Substances 0.000 claims description 9
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 8
- 239000008367 deionised water Substances 0.000 claims description 8
- 229910021641 deionized water Inorganic materials 0.000 claims description 8
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 claims description 8
- -1 polyethylene Polymers 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 238000009775 high-speed stirring Methods 0.000 claims description 5
- 229940057995 liquid paraffin Drugs 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 239000001993 wax Substances 0.000 claims description 5
- 229920000587 hyperbranched polymer Polymers 0.000 claims description 4
- 239000004149 tartrazine Substances 0.000 claims description 4
- 238000002347 injection Methods 0.000 claims description 3
- 239000007924 injection Substances 0.000 claims description 3
- 238000001746 injection moulding Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000008187 granular material Substances 0.000 claims description 2
- 238000005303 weighing Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 7
- 230000007774 longterm Effects 0.000 abstract description 6
- 238000005461 lubrication Methods 0.000 abstract description 6
- 239000010687 lubricating oil Substances 0.000 abstract description 5
- 230000014759 maintenance of location Effects 0.000 abstract description 5
- 239000011148 porous material Substances 0.000 abstract description 5
- 230000000149 penetrating effect Effects 0.000 abstract description 4
- 239000007787 solid Substances 0.000 abstract description 4
- 238000013329 compounding Methods 0.000 abstract description 3
- 229920003023 plastic Polymers 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 230000002035 prolonged effect Effects 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 12
- 238000010998 test method Methods 0.000 description 8
- 239000004952 Polyamide Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 229920002530 polyetherether ketone Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000010724 circulating oil Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000007723 die pressing method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a high-temperature-resistant self-lubricating motor bearing retainer, and relates to the technical field of plastic bearing retainers. The invention discloses a high-temperature-resistant self-lubricating motor bearing retainer which is prepared from a polyamide-based composite material and is prepared from the following raw materials: PA46/MPS matrix, surface modified halloysite nanotube, hyperbranched epoxy resin, composite dispersant, nucleating agent and lubricant; the PA46/MPS matrix is prepared by pre-treating mesoporous silica with a silane coupling agent and then compounding the mesoporous silica with PA 46; the mesoporous silica is an amino mesoporous silica nanoparticle. The high-temperature-resistant self-lubricating motor bearing retainer provided by the invention has high strength and toughness, excellent wear resistance, dimensional stability and water resistance, and the long-term working temperature can reach 200 ℃; the material contains a hollow pipe cavity and a penetrating nanoscale pore canal, so that a solid or liquid lubricant can infiltrate into the PA 46-based composite material, the material has good lubrication retention, the service life of the retainer is prolonged, and the cost is reduced.
Description
Technical Field
The invention belongs to the technical field of plastic bearing retainers, and particularly relates to a high-temperature-resistant self-lubricating motor bearing retainer.
Background
The driving motor is a key part of the new energy electric automobile, compared with the traditional automobile, the rotating speed of the driving motor of the new energy electric automobile is higher, the rotating speed can reach 16000r/min, the retainer surrounds the bearing rollaway nest, the balls are isolated and positioned at almost the same intervals, the retainer bears great centrifugal force, impact and vibration when the rolling bearing works, particularly when the load is complex and the rolling bearing rotates at a high speed, great sliding friction exists between the retainer and the rolling body, a great amount of heat is generated, the retainer is damaged as a result of the combined action of the force and the heat, and the retainer is burnt and broken when serious. Therefore, the cage material is required to have the characteristics of high strength, high toughness, high temperature resistance, corrosion resistance, good wear resistance, good thermal conductivity, light weight, good self-lubricating property and the like.
The cage can be classified into a metallic cage and a non-metallic cage according to the kind of material. The metal retainer is commonly used as a steel retainer and a brass retainer, the steel retainer has light weight, high strength, no limit of operating temperature, high-end shock resistance and acceleration resistance, but is sensitive to poor lubrication, and the selectivity of lubricant is higher; the brass retainer has extremely high strength, high shockproof and acceleration resistance, suitability for ultrahigh-speed operation related to circulating oil lubrication, but expensive raw materials and high cost. The nonmetallic material holder is lightweight, low in noise, and resistant to wear due to its porous structure, and is used as an oil reservoir (lubricating oil storage), and the nonmetallic holders commonly used are: polyimide, polyamideimide, polyetheretherketone, vespelTM, meldinTM, polyamide resin, phenolic resin and polytetrafluoroethylene. Polyimide, polyamide-imide, polyether-ether-ketone, vespel and MeldinTM are used as retainer materials, and have high strength, wear resistance and self-lubricity, the use temperature can reach 300 ℃, but the melting point is high, the molding is difficult, the die pressing sintering is generally adopted, the production process is complex, the cost is high, and the raw material cost is high. The phenolic resin has light weight, good wear resistance, good dimensional stability, long-term working temperature up to 120 ℃, but has higher toughness, easy fracture, poor alkali resistance and low molding productivity. The polytetrafluoroethylene retainer has excellent wear resistance, self-lubricating property and weather resistance, but has low heat conductivity coefficient, the thick-wall product cannot be quenched, the expansion coefficient is 10-20 times that of steel, the temperature is easy to change, the dimensional stability is poor, and the service life of the bearing is influenced. The polyamide material has the advantages of high elasticity and light weight, and the retainer has very good sliding and self-lubricating properties, but toughness is affected by temperature, and the water absorption rate is higher, so that the retainer is dehydrated in the use process, is easy to become brittle, and affects the use effect and service life.
The PA46 retainer is aliphatic polyamide formed by condensing butanediamine and adipic acid, and has a molecular structure similar to nylon 66, but the number of amide groups on a PA46 long chain is more, and the chain structure is more symmetrical; the highly symmetrical chain structure results in high crystallinity (about 70%), high crystallization rate, high heat distortion temperature, and long-term use temperature up to 163 ℃. The PA46 also has the characteristics of high strength, high wear resistance and the like, and has better mechanical strength and wear resistance at heat resistance and high temperature, but has larger water absorption and poorer dimensional stability, and influences the use of products.
Disclosure of Invention
The invention aims to provide a high-temperature-resistant self-lubricating motor bearing retainer which is prepared from a PA 46-based composite material, has high strength and toughness, excellent wear resistance, self-lubricating property, dimensional stability and water resistance, and can be used for long-term working at the temperature of up to 200 ℃; the PA 46-based composite material contains a hollow pipe cavity and a penetrating nanoscale pore canal, so that a solid or liquid lubricant can infiltrate into the PA 46-based composite material, the self-lubricity of the retainer is improved, the retainer has good lubrication retention, the wear resistance of the retainer is enhanced, the service life of the retainer is prolonged, and the cost is reduced.
In order to achieve the purpose of the invention, the invention provides a high-temperature-resistant self-lubricating motor bearing retainer which is prepared from a polyamide-based composite material, wherein the polyamide-based composite material comprises the following raw materials in parts by weight: 60-85 parts of PA46/MPS matrix, 10-30 parts of surface modified halloysite nanotube, 5-10 parts of hyperbranched epoxy resin, 3-5 parts of composite dispersing agent, 0.3-0.5 part of nucleating agent and 1-2 parts of lubricant;
the PA46/MPS matrix is prepared by pretreating mesoporous silica by a silane coupling agent and then compounding the mesoporous silica with PA 46;
the mesoporous silica is an amino mesoporous silica nanoparticle.
Further, the preparation method of the PA46/MPS matrix comprises the following steps: and (3) placing mesoporous silica into deionized water, uniformly mixing, adding a silane coupling agent, stirring for 1-2 hours, adding PA46, heating to 70-80 ℃, stirring for reacting for 2-3 hours, filtering, and drying to obtain the PA46/MPS matrix.
Further, the usage amount of the deionized water is 2 times of the mass of the mesoporous silica;
the silane coupling agent is silane coupling agent KH-792, and the mass ratio of the silane coupling agent to the mesoporous silica is (0.3-0.5): 1, a step of;
the mass ratio of the PA46 to the mesoporous silica is 1: (0.05-0.08).
Further, the preparation method of the surface modified halloysite nanotube comprises the following steps: immersing halloysite nanotubes in 8wt% dilute hydrochloric acid, stirring for 30-40 min, and then filtering, washing and drying to obtain pretreated halloysite nanotubes; and (3) placing the pretreated halloysite nanotube in a high-speed kneader, spraying liquid paraffin and a titanate coupling agent KR-TTS with the mass ratio of 2:1 under high-speed stirring, heating to 60-70 ℃, and continuously stirring for 15-20 min to obtain the surface modified halloysite nanotube.
Further, the adding amount of the titanate coupling agent KR-TTS is 0.5-1.0% of the mass of the pretreated halloysite nanotube.
Further, the hyperbranched epoxy resin is hyperbranched epoxy resin HyPer E102 provided by Wuhan hyperbranched resin technology Co.
Further, the composite dispersing agent comprises the following components in percentage by mass: the polyethylene wax is compounded with 1 ethylene bis stearamide.
Further, the nucleating agent is Licom Cav102 of Craien or P22 of Bulgerman.
Further, the lubricant is a hyperbranched polymer, and is any one of HBP-160, hyPer C100, hyPer C181 or HyPer C182 provided by Wuhan hyperbranched resin technology Co.
The invention also provides a preparation method of the high-temperature-resistant self-lubricating motor bearing retainer, which comprises the following steps:
p1, weighing required raw materials according to parts by weight, adding a PA46/MPS matrix and hyperbranched epoxy resin into a mixer, stirring at a high speed for 3-5 min, wherein the stirring speed is 360r/min, heating to 50-60 ℃, adding a surface modified halloysite nanotube and a composite dispersing agent, stirring at a high speed for 5-8 min, and stirring at a speed of 360r/min to obtain a mixture;
p2, uniformly mixing the mixture, the nucleating agent and the lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, extruding and granulating to obtain a polyamide-based composite material, and then carrying out injection molding on the granules, wherein the injection temperature is set to 270-300 ℃, thus obtaining the required high-temperature-resistant self-lubricating motor bearing retainer.
The invention has the following beneficial effects:
1. according to the invention, the PA46/MPS (mesoporous silica) composite material is adopted as a matrix of the retainer, MPS is placed in deionized water and uniformly mixed, then a silane coupling agent is added, so that the hydrolyzed silane coupling agent is combined with the MPS, silane modification is carried out on the surface of the MPS, the surface activity of the MPS is not easy to agglomerate, the interfacial binding force of the MPS and the PA46 is improved, the PA46 is added, the silane modified MPS is combined with the PA46, meanwhile, the specific surface area of the PA46/MPS composite material is increased, and the PA46/MPS composite material is better compatible with components such as surface modified halloysite nanotubes, hyperbranched epoxy resin, composite dispersing agents and the like, so that the mechanical strength, wear resistance, self-lubricating property and long-term use temperature of the polyamide composite material are improved, and the polyamide composite material has high toughness and excellent processing performance and the processing temperature is not influenced. The mesoporous silica is added, so that the polyamide-based composite material contains a large number of penetrating nanoscale pore channels, the specific surface area and the adsorptivity of the retainer are increased, and therefore, solid or liquid lubricant can be soaked into the penetrating pore channels of the polyamide composite material, and the self-lubricity of the bearing retainer is improved; the adsorption of mesoporous silica also makes the adsorbed lubricant not easy to separate out, so that the lubricant has better lubrication retention.
2. The halloysite nanotube is of a hollow tubular structure with high length-diameter ratio, the inner cavity of the nanotube is mainly aluminum hydroxyl, the outer part of the nanotube is mainly siloxane, and a small amount of silicon hydroxyl and aluminum hydroxyl are exposed at the edge, so that the nanotube has excellent adsorptivity and catalytic activity. According to the invention, the halloysite nanotube is firstly treated by dilute hydrochloric acid, impurities in the inner cavity of the nanotube are removed, the porosity of the halloysite nanotube is increased, the specific surface and the adsorptivity of the halloysite nanotube are improved, then the pretreated halloysite nanotube is subjected to surface modification by adopting a diluted titanic acid coupling agent, the surface activity of the halloysite nanotube is increased, the interfacial binding force of the halloysite nanotube and each component in the polyamide-based composite material is improved, so that the PA46/MPS matrix can be better compatible, the mechanical strength, the high temperature resistance and the wear resistance of the polyamide-based composite material are further improved, and the solid or liquid lubricant can be impregnated into the pores of the polyamide-based composite material, so that the self-lubricating property of the bearing retainer is improved. The excellent adsorptivity of the surface modified halloysite nanotube also makes the adsorbed lubricant not easy to separate out, so that the surface modified halloysite nanotube has better lubrication retention.
3. The hyperbranched epoxy resin HyPer E102 added in the invention has low viscosity, high epoxy value and high activity, and improves the strength and toughness of the polyamide-based composite material; the hyperbranched epoxy resin has high activity, so that other components in the polyamide-based composite material are easy to combine, the waterproof property of the composite material is improved, and the water absorption rate of the composite material is reduced; the hyperbranched epoxy resin has low viscosity and high epoxy value, improves the processing performance of the invention, reduces the processing temperature of the invention and saves the cost.
4. The dispersing agent is prepared by compounding Ethylene Bis Stearamide (EBS) and polyethylene wax. The EBS is a dispersant containing polar groups and nonpolar groups, has excellent dispersant on organic polymers or inorganic fillers, and has synergistic effect with polyethylene wax, so that the dispersibility of each component in the polyamide-based composite material is greatly improved, the components are uniformly dispersed, the strength of the polyamide-based composite material is improved to a certain extent, the compatibility between a PA46/MPS matrix and other components is improved, and the mechanical property of the PA 46-based composite material is improved.
5. The lubricant disclosed by the invention is a hyperbranched polymer and has good thermal stability and migration resistance. The addition of the lubricant obviously improves the processing performance of the invention, improves the dispersing agent of each component in the polyamide-based composite material, increases the compatibility between each component and the PA46/MPS matrix, and improves the long-term use temperature of the invention.
6. The invention adopts PA46/MPS composite material as a matrix, and adopts the surface modified halloysite nanotube, hyperbranched epoxy resin, composite dispersant, lubricant and the like to carry out modification, thus preparing the high-temperature resistant self-lubricating motor bearing retainer adopting the polyamide composite material, which has excellent wear resistance, self-lubricating property, dimensional stability and water resistance, and the working temperature can reach 200 ℃ at most. The polyamide-based composite material also has better self-lubricating retention, enhances the wear resistance of the retainer, prolongs the service life of the retainer and reduces the production cost.
Detailed Description
The following description of the embodiments of the present invention will be made clearly and completely, and it is apparent that the described embodiments are only some embodiments of the present invention, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
The amino mesoporous silica nanoparticle used in the invention is provided by Nanjing-based biotechnology Co., ltd, and has a particle size of 300nm.
The lubricant used in the invention is hyperbranched polymer, which is provided by the Wuhan hyperbranched resin technology Co., ltd.
The hyperbranched epoxy resin used in the invention is hyperbranched epoxy resin HyPer E102 provided by Wuhan hyperbranched resin technology Co.
The titanate coupling agent KR-TTS used in the present invention is produced by Kenrich Petroleum Inc. in U.S.A.
The halloysite nanotube used in the invention is provided by Nanjing Xianfeng nano material science and technology Co., ltd, and the model is XFI50.
The PA46 in the present embodiment uses TS350 from desiman, netherlands.
The nucleating agent in the embodiment of the invention uses the P22 of Bulgerman, and can also be replaced by Licom Cav102 of Craien.
The high temperature resistant self-lubricating motor bearing retainer of the present invention is described below with reference to specific embodiments.
The high-temperature-resistant self-lubricating motor bearing retainer is prepared by injection molding of a polyamide-based composite material, and the injection temperature is 270-300 ℃.
Example 1
A preparation method of the polyamide-based composite material comprises the following steps: adding 60 parts of PA46/MPS matrix and 30 parts of hyperbranched epoxy resin into a mixer, stirring at a high speed for 4min, heating to 50 ℃, adding 30 parts of surface modified halloysite nanotubes and 5 parts of composite dispersing agent, and stirring at a high speed for 8min, wherein the stirring speed is 360r/min to obtain a mixture; and (3) uniformly mixing the mixture, 0.3 part of nucleating agent and 1 part of lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, and extruding and granulating to obtain the polyamide-based composite material.
The preparation method of the PA46/MPS matrix comprises the following steps: according to the weight portions, 5 portions of mesoporous silica are placed in 10 portions of deionized water to be uniformly mixed, then 1.5 portions of silane coupling agent KH-792 is added, stirring is carried out for 2 hours, 100 portions of PA46 are added, heating is carried out to 80 ℃, stirring is carried out for 2 hours, filtering is carried out, and drying is carried out, thus obtaining the PA46/MPS matrix.
The preparation method of the surface modified halloysite nanotube comprises the following steps: immersing 100 parts of halloysite nanotubes in 8wt% of dilute hydrochloric acid, stirring for 30min, and then filtering, washing and drying to obtain pretreated halloysite nanotubes; and (3) placing the pretreated erloting nanotube in a high-speed kneader, spraying 1 part of liquid paraffin and 0.5 part of titanate coupling agent KR-TTS in a mist manner under high-speed stirring, and heating to 70 ℃ and continuously stirring for 15min to obtain the surface modified halloysite nanotube.
The lubricant is HBP-160 provided by Wuhan hyperbranched resin technology Co.
Example 2
A preparation method of the polyamide-based composite material comprises the following steps: according to parts by weight, 85 parts of PA46/MPS matrix and 10 parts of hyperbranched epoxy resin are added into a mixer, the mixture is stirred at a high speed for 5min, the stirring speed is 360r/min, the temperature is raised to 60 ℃, 10 parts of surface modified halloysite nanotubes and 3 parts of composite dispersing agent are added, the mixture is stirred at a high speed for 8min, and the stirring speed is 360r/min, so that a mixture is obtained; and (3) uniformly mixing the mixture, 0.5 part of nucleating agent and 1 part of lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, and extruding and granulating to obtain the polyamide-based composite material.
The preparation method of the PA46/MPS matrix comprises the following steps: according to the parts by weight, placing 8 parts of mesoporous silica into 16 parts of deionized water, uniformly mixing, adding 4 parts of silane coupling agent KH-792, stirring for 1h, adding 100 parts of PA46, heating to 70 ℃, stirring for 4h, filtering, and drying to obtain the PA46/MPS matrix.
The preparation method of the surface modified halloysite nanotube comprises the following steps: immersing 100 parts of halloysite nanotubes in 8wt% of dilute hydrochloric acid, stirring for 30min, and then filtering, washing and drying to obtain pretreated halloysite nanotubes; and (3) placing the pretreated erloting nanotube in a high-speed kneader, spraying 2 parts of liquid paraffin and 1 part of titanate coupling agent KR-TTS in a mist manner under high-speed stirring, and heating to 70 ℃ and continuing stirring for 15min to obtain the surface modified halloysite nanotube.
The lubricant is HyPer C181 provided by Wuhan hyperbranched resin technology Co.
Example 3
A preparation method of the polyamide-based composite material comprises the following steps: adding 65 parts of PA46/MPS matrix and 5 parts of hyperbranched epoxy resin into a mixer, stirring at a high speed for 5min, wherein the stirring speed is 360r/min, heating to 60 ℃, adding 30 parts of surface modified halloysite nanotubes and 5 parts of composite dispersing agent, and stirring at a high speed for 8min, wherein the stirring speed is 360r/min to obtain a mixture; and (3) uniformly mixing the mixture, 0.3 part of nucleating agent and 2 parts of lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, and extruding and granulating to obtain the polyamide-based composite material.
The preparation method of the PA46/MPS matrix comprises the following steps: and (3) placing 6 parts of mesoporous silica into 12 parts of deionized water according to parts by weight, uniformly mixing, adding 2.5 parts of silane coupling agent KH-792, stirring for 2 hours, adding 100 parts of PA46, heating to 60 ℃, stirring for 4 hours, filtering, and drying to obtain the PA46/MPS matrix.
The preparation method of the surface modified halloysite nanotube comprises the following steps: immersing 100 parts of halloysite nanotubes in 8wt% of dilute hydrochloric acid, stirring for 30min, and then filtering, washing and drying to obtain pretreated halloysite nanotubes; and placing the pretreated erloting nanotube in a high-speed kneader, spraying 1.6 parts of liquid paraffin and 0.8 part of titanate coupling agent KR-TTS under high-speed stirring, heating to 70 ℃ and continuously stirring for 15min to obtain the surface modified halloysite nanotube.
The lubricant is HyPer C182 provided by Wuhan hyperbranched resin technology Co.
Example 4
A preparation method of the polyamide-based composite material comprises the following steps: adding 75 parts of PA46/MPS matrix and 5 parts of hyperbranched epoxy resin into a mixer, stirring at a high speed for 5min, heating to 60 ℃, adding 20 parts of surface modified halloysite nanotubes and 4 parts of composite dispersing agent, and stirring at a high speed for 8min, wherein the stirring speed is 360r/min to obtain a mixture; and (3) uniformly mixing the mixture, 0.4 part of nucleating agent and 2 parts of lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, and extruding and granulating to obtain the polyamide-based composite material.
The preparation method of the PA46/MPS matrix is the same as that in example 3, and specific reference is made to example 3.
The preparation method of the surface-modified halloysite nanotube is the same as that of example 3, and specific reference is made to example 3.
The lubricant is HyPer C100 provided by Wuhan hyperbranched resin technology Co.
Example 5
A preparation method of the polyamide-based composite material comprises the following steps: adding 70 parts of PA46/MPS matrix and 8 parts of hyperbranched epoxy resin into a mixer, stirring at a high speed for 5min, heating to 60 ℃, adding 22 parts of surface modified halloysite nanotubes and 4 parts of composite dispersing agent, and stirring at a high speed for 8min, wherein the stirring speed is 360r/min to obtain a mixture; uniformly mixing the mixture, 0.35 part of nucleating agent and 1.5 parts of lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, and extruding and granulating to obtain the polyamide-based composite material.
The preparation method of the PA46/MPS matrix is the same as that in example 3, and specific reference is made to example 3.
The preparation method of the surface-modified halloysite nanotube is the same as that of example 3, and specific reference is made to example 3.
The lubricant is HBP-160 provided by Wuhan hyperbranched resin technology Co.
Comparative example 1
A polyamide-based composite material was prepared in the same manner as in example 5, except that the PA46/MPS matrix was not added but 70 parts of PA46 was added in comparative example 1.
Comparative example 2
A polyamide-based composite material was the same as in example 5 in composition, raw materials and preparation method, except that no surface-modified halloysite nanotube was added in comparative example 2, and 92 parts of PA46/MPS matrix was added.
Comparative example 3
The composition, raw materials and preparation method of the polyamide-based composite material are the same as those in example 5, except that hyperbranched epoxy resin is not added in comparative example 3, 78 parts of PA46/MPS matrix are added, and the temperature of a screw extruder is 270-300 ℃.
Comparative example 4
A polyamide-based composite material was prepared in the same manner as in example 5, except that the dispersant in comparative example 4 was 4 parts of Ethylene Bis Stearamide (EBS).
Comparative example 5
A polyamide-based composite material was prepared in the same manner as in example 5, except that the lubricant in comparative example 5 was oleamide and the temperature of the screw extruder was 280 to 310 ℃.
The polyamide-based composite materials obtained in examples 1 to 5 and comparative examples 1 to 5 were subjected to performance test, and the test results are shown in tables 1 to 2 below.
The detection method comprises the following steps:
the water absorption test method refers to GB/T1034-2008, and soaking is carried out for 24+/-1 h at the temperature of 23 ℃;
the tensile stress test method is tested with reference to ISO 572-2-2012 at 120 ℃;
the tensile modulus test method was tested with reference to ISO 572-2-2012 at 120 ℃; the method comprises the steps of carrying out a first treatment on the surface of the
The notch impact strength test method refers to ISO 180-2000;
the linear thermal expansion coefficient test method is tested by referring to ISO 11359-2-1999;
the glass transition temperature test method is tested with reference to ASTM D3418-08;
the shrinkage test method is carried out according to GB/T15585-1995;
the coefficient of friction test method was examined with reference to GB/T10006-1998.
Table 1 shows the results of the Performance test of the Polyamide-based composite materials of examples 1 to 5
TABLE 2 Polyamide-based composite Performance test results Table for example 5 and comparative examples 1-5
From the detection results in tables 1 and 2, the addition of mesoporous silica and modified halloysite nanotubes in the polyamide-based composite material of the invention significantly improves the mechanical strength, toughness, water resistance, high temperature resistance, thermal stability and wear resistance of the invention; the addition of hyperbranched epoxy resin obviously improves the water resistance of the invention; the addition of the lubricant improves the high temperature resistance and the processability of the invention; the ethylene bis stearamide and the polyethylene wax are used in a combined way, so that the comprehensive performance of the invention is improved.
The technical features of the above-described embodiments may be arbitrarily combined, and all possible combinations of the technical features in the above-described embodiments are not described for brevity of description, however, as long as there is no contradiction between the combinations of the technical features, they should be considered as the scope of the description.
The foregoing examples illustrate only a few embodiments of the invention and are described in detail herein without thereby limiting the scope of the invention. It should be noted that it will be apparent to those skilled in the art that several variations and modifications can be made without departing from the spirit of the invention, which are all within the scope of the invention.
Claims (2)
1. The high-temperature-resistant self-lubricating motor bearing retainer is prepared from a polyamide-based composite material, and is characterized in that the polyamide-based composite material comprises the following raw materials in parts by weight: 60-85 parts of PA46/MPS matrix, 10-30 parts of surface modified halloysite nanotube, 5-10 parts of hyperbranched epoxy resin HyPer E102, 3-5 parts of composite dispersing agent, 0.3-0.5 part of nucleating agent and 1-2 parts of lubricant;
the preparation method of the PA46/MPS matrix comprises the following steps: uniformly mixing mesoporous silica in deionized water, adding a silane coupling agent, stirring for 1-2 h, adding PA46, heating to 70-80 ℃, stirring for reacting for 2-3 h, filtering, and drying to obtain a PA46/MPS matrix;
the usage amount of the deionized water is 2 times of the mass of the mesoporous silica;
the silane coupling agent is silane coupling agent KH-792, and the mass ratio of the silane coupling agent to the mesoporous silica is (0.3-0.5): 1, a step of;
the mass ratio of the PA46 to the mesoporous silica is 1: (0.05-0.08);
the mesoporous silica is amino mesoporous silica nano-particles;
the preparation method of the surface modified halloysite nanotube comprises the following steps: immersing halloysite nanotubes in 8wt% dilute hydrochloric acid, stirring for 30-40 min, and then filtering, washing and drying to obtain pretreated halloysite nanotubes; placing the pretreated halloysite nanotube in a high-speed kneader, spraying liquid paraffin and titanate coupling agent KR-TTS with the mass ratio of 2:1 under high-speed stirring, heating to 60-70 ℃ and continuously stirring for 15-20 min to obtain the surface modified halloysite nanotube;
the adding amount of the titanate coupling agent KR-TTS is 0.5-1.0% of the mass of the pretreated halloysite nanotube;
the composite dispersing agent comprises the following components in percentage by mass: 1 ethylene bis stearamide and polyethylene wax are compounded;
the nucleating agent is Licom Cav102 of Craien or P22 of Bulgerman;
the lubricant is hyperbranched polymer and is any one of HBP-160, hyPer C100, hyPer C181 or HyPer C182 provided by Wuhan hyperbranched resin technology Co.
2. A method for preparing the high temperature resistant self-lubricating motor bearing retainer as claimed in claim 1, which is characterized by comprising the following steps:
p1, weighing required raw materials according to parts by weight, adding a PA46/MPS matrix and hyperbranched epoxy resin into a mixer, stirring at a high speed for 3-5 min, wherein the stirring speed is 360r/min, heating to 50-60 ℃, adding a surface modified halloysite nanotube and a composite dispersing agent, stirring at a high speed for 5-8 min, and stirring at a speed of 360r/min to obtain a mixture;
p2, uniformly mixing the mixture, the nucleating agent and the lubricant, adding the mixture into a screw extruder, setting the temperature of the screw extruder to 260-290 ℃, extruding and granulating to obtain a polyamide-based composite material, and then carrying out injection molding on the granules, wherein the injection temperature is set to 270-300 ℃, thus obtaining the required high-temperature-resistant self-lubricating motor bearing retainer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211126100.XA CN115746551B (en) | 2022-09-16 | 2022-09-16 | High temperature resistant self-lubricating motor bearing holder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211126100.XA CN115746551B (en) | 2022-09-16 | 2022-09-16 | High temperature resistant self-lubricating motor bearing holder |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115746551A CN115746551A (en) | 2023-03-07 |
CN115746551B true CN115746551B (en) | 2024-01-19 |
Family
ID=85350185
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202211126100.XA Active CN115746551B (en) | 2022-09-16 | 2022-09-16 | High temperature resistant self-lubricating motor bearing holder |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN115746551B (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108976782A (en) * | 2018-06-15 | 2018-12-11 | 湖南工业大学 | A kind of nylon composite materials and preparation method thereof modified based on hyperbranched epoxy resin |
CN109438975A (en) * | 2018-11-26 | 2019-03-08 | 北京航天试验技术研究所 | A kind of high-strength nylon composite material and preparation method |
-
2022
- 2022-09-16 CN CN202211126100.XA patent/CN115746551B/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108976782A (en) * | 2018-06-15 | 2018-12-11 | 湖南工业大学 | A kind of nylon composite materials and preparation method thereof modified based on hyperbranched epoxy resin |
CN109438975A (en) * | 2018-11-26 | 2019-03-08 | 北京航天试验技术研究所 | A kind of high-strength nylon composite material and preparation method |
Also Published As
Publication number | Publication date |
---|---|
CN115746551A (en) | 2023-03-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Nie et al. | Preparation and tribological properties of polyimide/carboxyl-functionalized multi-walled carbon nanotube nanocomposite films under seawater lubrication | |
CN110776734B (en) | Wear-resistant hydrolysis-resistant alcohol depolymerized amide composite material and preparation method and application thereof | |
CN101864168B (en) | Wear-resistant self-lubricating nylon compound material and method for preparing same | |
CN108795041B (en) | Nano MoS2Carbon nano tube/bismaleimide resin composite material and preparation method thereof | |
CN115322566B (en) | PA 66-based composite material for motor bearing retainer and preparation method thereof | |
CN105524405A (en) | Antistatic peek composite material and preparation method thereof | |
CN112322033B (en) | Low-crystallization-temperature high-performance polyamide composite material | |
CN116376197A (en) | Polytetrafluoroethylene sealing material and preparation method thereof | |
CN114645451A (en) | Layered composite material and preparation method thereof, self-lubricating fiber fabric composite material and preparation method and application thereof | |
CN1168781C (en) | Self-lubricating nano composite material and its preparation method | |
CN109486069A (en) | Wear-resisting PTFE composite and preparation method thereof | |
CN115746551B (en) | High temperature resistant self-lubricating motor bearing holder | |
Yan et al. | Surface wettability, tensile mechanical performance, and tribological behavior of polyimide/polytetrafluoroethylene blends enhanced with hydroxylated multiwalled carbon nanotubes at high relative humidity | |
CN110982262A (en) | Wear-resistant reinforced long-carbon-chain nylon PA1012 composite material and preparation method thereof | |
US20150126663A1 (en) | Tribological aromatic polyimide compositions | |
CN105524412A (en) | Antistatic peek resin material and preparation method thereof | |
CN100364718C (en) | Method for preparing sliding bearing of nano AI2O3/polyimide friction compound material | |
CN111793355B (en) | Wear-resistant PPO/PA66 alloy material for automobile wiper shaft sleeve and preparation method thereof | |
CN114990729A (en) | Wear-resistant nylon yarn and preparation method thereof | |
CN108384186B (en) | Polyether-ether-ketone composite material for bearing and preparation method thereof | |
JPS6345694B2 (en) | ||
CN105754335B (en) | Mechanical arm element of a kind of high-intensity welding and preparation method thereof | |
CN114381113A (en) | Preparation method of self-lubricating high-wear-resistance fluorine-containing polymer alloy | |
CN111393799A (en) | Antifriction wear-resistant carbon nanocage/epoxy resin self-lubricating composite material and preparation method thereof | |
CN111704797A (en) | Low-warpage, conductive and high-mechanical-property fiber-reinforced nylon composite material and preparation method thereof |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant |