CN110684324A - Nano-alumina particle modified PET polyester and formed automobile guide ball pin - Google Patents

Nano-alumina particle modified PET polyester and formed automobile guide ball pin Download PDF

Info

Publication number
CN110684324A
CN110684324A CN201910933152.XA CN201910933152A CN110684324A CN 110684324 A CN110684324 A CN 110684324A CN 201910933152 A CN201910933152 A CN 201910933152A CN 110684324 A CN110684324 A CN 110684324A
Authority
CN
China
Prior art keywords
pet polyester
nano
alumina particles
glycidyl methacrylate
ball pin
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.)
Granted
Application number
CN201910933152.XA
Other languages
Chinese (zh)
Other versions
CN110684324B (en
Inventor
沈百庆
朱惠全
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.)
SOMIC AUTOMOTIVE COMPONENTS CO Ltd
Original Assignee
SOMIC AUTOMOTIVE COMPONENTS CO Ltd
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 SOMIC AUTOMOTIVE COMPONENTS CO Ltd filed Critical SOMIC AUTOMOTIVE COMPONENTS CO Ltd
Priority to CN201910933152.XA priority Critical patent/CN110684324B/en
Publication of CN110684324A publication Critical patent/CN110684324A/en
Application granted granted Critical
Publication of CN110684324B publication Critical patent/CN110684324B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • C08K9/06Ingredients treated with organic substances with silicon-containing compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B62LAND VEHICLES FOR TRAVELLING OTHERWISE THAN ON RAILS
    • B62DMOTOR VEHICLES; TRAILERS
    • B62D7/00Steering linkage; Stub axles or their mountings
    • B62D7/18Steering knuckles; King pins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Transportation (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Discloses a PET polyester, which is obtained by blending and modifying PET polyester and alumina particles; the alumina particles are nano-scale alumina particles. In addition, the automobile guide ball pin is made of a material formed by melt blending of polycarbonate and the PET polyester. The automobile guide ball pin not only has higher impact strength, but also has higher elongation at break; the related technical indexes can fully meet the performance requirements of the automobile guide ball pin.

Description

Nano-alumina particle modified PET polyester and formed automobile guide ball pin
Technical Field
The invention belongs to the field of automobile materials; relates to a material for a guide ball pin of an automobile; more particularly, the invention relates to PET polyester modified by nano alumina particles and a formed automobile guide ball pin.
Background
The guide ball pin is an important part on the automobile and is used for controlling the steering of the automobile. Long-time, the structure of direction ball round pin is comparatively complicated, needs the form fit through ball seat and cylindrical casing just can rotate, and operation and equipment convenience are poor, have improved the processing cost of car to a certain extent. In addition, the structure is complex, so that the guide ball pin is worn seriously under long-term tensile and pressure load bearing, the service life is short, and the reliability requirement of long-term use is difficult to meet.
The inventor uses PET polyester as synthetic resin to form a small ball seat in Chinese utility model CN200820165818, and replaces the original steel wire small ball. The material has better elasticity, has larger matching surface, increases the friction surface, plays a role in compensating the abrasion of the product, and has excellent rotation performance and tensile pressure.
However, the use of PET polyester as a material for ball seats of guide ball pins for automobiles has disadvantages of low notched impact strength and low elongation at break.
To ameliorate these technical deficiencies, polycarbonate has further been alloyed with PET polyester. By virtue of the advantages of the amorphous polycarbonate polymer, the alloy formed by the amorphous polycarbonate polymer has excellent impact resistance and dimensional stability. Zengbanlu et al (polymer materials science and engineering, 1991, 110-.
Because PET polyester is a crystalline polymer and polycarbonate is an amorphous polymer, a simple blending system formed by the PET polyester and the polycarbonate is easy to generate phase separation, the bonding force of a two-phase interface is poor, and the notch impact strength is difficult to improve.
Therefore, the further research on the PET polyester modified by the nano-alumina particles and the automobile guide ball pin formed by the PET polyester is urgently needed on the basis of the prior art.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provide the PET polyester modified by the nano-alumina particles with higher notch impact strength and higher elongation at break.
The invention also aims to provide the automobile guide ball pin formed by the PET.
In order to achieve the above object, in one aspect, the present invention provides a PET polyester obtained by blending and modifying PET polyester and alumina particles; characterized in that the alumina particles are nano-scale alumina particles.
The PET polyester according to the present invention, wherein nanoscale represents a particle size range having an average particle size of 1 to 1000 nm. Preferably, nanoscale means a particle size range having an average particle size of 10 to 900 nm; more preferably, nanoscale means a particle size range having an average particle size of 50 to 700 nm; and, most preferably, nanoscale means a particle size range having an average particle size of 100-500 nm.
In a particular embodiment, the nanoscale alumina is selected from alumina powders having an average particle size of 320 nm.
The PET polyester provided by the invention has the number average molecular weight Mn of 30000-46000 daltons.
Preferably, the number average molecular weight Mn of the PET polyester is 32000-44000 dalton; more preferably, the number average molecular weight Mn of the PET polyester is 34000 and 42000 daltons; and, most preferably, the number average molecular weight Mn of the PET polyester is 36000-40000 Dalton.
In a particular embodiment, the PET polyester has a number average molecular weight Mn of 38500 daltons.
The PET polyester is characterized in that the nanoscale alumina particles are further modified by glycidyl methacrylate.
In a specific embodiment, the glycidyl methacrylate is obtained from Shandong Yukang chemical Co., Ltd, and has a purity of 99.9%.
The PET polyester provided by the invention is characterized in that the grafting ratio of glycidyl methacrylate of the nanoscale alumina particles is 8.0-18.0%.
Preferably, the grafting ratio of the glycidyl methacrylate of the nano-scale alumina particles is 9.0-17.0%; more preferably, the nano-scale alumina particles have a glycidyl methacrylate grafting ratio of 10.0 to 16.0%; and, most preferably, the nano-sized alumina particles have a glycidyl methacrylate grafting ratio of 11.3 to 15.4%.
In a specific embodiment, the nano-sized alumina particles have a glycidyl methacrylate grafting ratio of 13.8%.
The PET polyester according to the invention wherein the grafting ratio is obtained from TGA data.
The PET polyester is characterized in that the nanoscale alumina particles are obtained by reacting nanoscale alumina powder with a silane coupling agent and then polymerizing the nanoscale alumina powder with glycidyl methacrylate.
The PET polyester according to the invention, wherein the silane coupling agent is a silane coupling agent having a polymerizable group.
Preferably, the polymerizable group is selected from the group consisting of vinyl, ethynyl, epoxy, and (meth) acryloxy; more preferably, the polymerizable group is selected from vinyl and (meth) acryloxy; and, most preferably, the polymerizable group is selected from (meth) acryloxy groups.
In a specific embodiment, the silane coupling agent is a silane coupling agent having a methacryloxypropyl group.
In a more specific embodiment, the silane coupling agent is selected from the group consisting of KH-570, 99.8% purity; purchased from Nanjing to the front chemical Co.
The PET polyester of the invention is characterized in that the weight ratio of the nanoscale alumina powder, the silane coupling agent and the glycidyl methacrylate is 10: (3-9): (4-15).
Preferably, the weight ratio of the nanoscale alumina powder, the silane coupling agent and the glycidyl methacrylate is 10: (3-8): (5-14); more preferably, the weight ratio of the nanoscale alumina powder, the silane coupling agent and the glycidyl methacrylate is 10: (4-7): (5-13); and, most preferably, the weight ratio of the nanoscale alumina powder, the silane coupling agent, and the glycidyl methacrylate is 10: (4-6): (6-12).
In a specific embodiment, the weight ratio of the nanoscale alumina powder, the silane coupling agent, and the glycidyl methacrylate is 10: 5: 10.
the PET polyester provided by the invention is characterized in that the weight ratio of the nanoscale alumina particles to the PET polyester is 1: (2-8).
Preferably, the weight ratio of the nano-alumina particles to the PET polyester is 1: (3-7); more preferably, the weight ratio of the nano-alumina particles to the PET polyester is 1: (3.5-6.5); and, most preferably, the weight ratio of the nano-sized alumina particles to the PET polyester is 1: (4-6).
In a specific embodiment, the weight ratio of the nano-alumina particles to the PET polyester is 1: 5.
in another aspect, the invention provides an automobile guide ball pin, which is characterized by being made of a material formed by melt blending polycarbonate and PET polyester according to the invention.
The automobile guide ball pin provided by the invention is characterized in that the weight ratio of the polycarbonate to the PET polyester is (60-80): (40-20).
Preferably, the weight ratio of the polycarbonate to the PET polyester is (65-75): (40-25); more preferably, the weight ratio of the polycarbonate to the PET polyester is (60-75): (40-25); and, most preferably, the weight ratio of the polycarbonate to the PET polyester is (60-70): (40-30).
In a specific embodiment, the weight ratio of the polycarbonate to the PET polyester is 65: 35.
the automobile guide ball pin provided by the invention has the advantages that the number average molecular weight Mn of the polycarbonate is 14000-30000 daltons.
Preferably, the number average molecular weight Mn of the polycarbonate is 16000 and 28000 daltons; more preferably, the number average molecular weight Mn of the polycarbonate is 18000 and 26000 daltons; and, most preferably, the number average molecular weight Mn of the polycarbonate is 20000-.
In a specific embodiment, the polycarbonate has a number average molecular weight Mn of 22000 daltons.
Advantageously, the material of the automotive guide ball pin according to the invention is formed by melt blending in a twin-screw extruder.
The inventor finds that the alloy material obtained by using the modified PET polyester obtained by modifying the nano-alumina particles and the polycarbonate has high impact strength and high elongation at break. Without wishing to be bound by any theory, the modified nanoscale alumina particles used in the invention not only play a role in improving the toughness of the material of the ball seat of the automobile guide ball pin, but also promote the compatibility with a resin system through the reactivity of methacryloxypropyl on the surface of alumina, and further improve the notch impact strength and the elongation at break of the material of the ball seat of the automobile guide ball pin.
Compared with the prior art, the invention has the following beneficial technical effects:
i) the automobile guide ball pin has excellent notch impact strength and elongation at break, and the notch impact strength is more than or equal to 50KJ × m-2And the elongation at break is more than or equal to 130 percent; so that the performance requirement of the ball seat for the automobile guide ball pin can be fully met.
ii) the method of the invention is simple and easy to implement, easy to popularize and has higher practical value.
Detailed Description
In a specific embodiment of the invention, the notched impact strength test is performed according to ASTM D256-2018, the impact energy is 2.8J, and the test specimens from test group 5 are averaged.
Elongation at break tests were performed according to ASTM D638-2014, with a tensile rate of 10mm/min, a test temperature of room temperature, and an average of 5 test specimens tested.
The TGA test was carried out using a Q500 thermogravimetric analyzer of TA, with a temperature rise rate of 10 degrees/min from room temperature to 700 degrees under a nitrogen atmosphere.
The grafting rate of the modified nanoscale alumina was obtained from the TGA data.
Example 1:
10g of nano-sized alumina powder (average particle size: 320nm) and 5g of silane coupling agent KH570 were ultrasonically dispersed in toluene, reacted with stirring at 120 ℃ for 4 hours in a nitrogen atmosphere, and then cooled to room temperature. 8g of glycidyl methacrylate dissolved in toluene and a few drops of AIBN were added and the reaction was stirred at 80 ℃ for 2 hours under a nitrogen atmosphere. After centrifugal drying, acetone extraction is used for removing unreacted coupling agent and residual toluene solvent, finally drying is carried out, modified nanometer alumina particles are obtained, and the grafting rate of glycidyl methacrylate obtained by TGA data is 13.8 wt%.
Preheating 8g of modified nano-alumina particles at 90 ℃, adding the modified nano-alumina particles into 40g of PET polyester preheated and melted at 90 ℃, and stirring the PET polyester under vacuum for 2.5h to ensure that the modified PET polyester is uniformly mixed with the PET polyester, wherein the number average molecular weight Mn of the PET polyester is 38500 daltons.
65g of polycarbonate (the number average molecular weight Mn is 22000 dalton) and 35g of modified PET polyester are uniformly mixed, and then the mixture is added into a double-screw extruder to be extruded and granulated, wherein the extrusion processing temperature is controlled between 240 +/-2 ℃, and the rotation speed of a screw is 400 rpm. Then, the extruded and cut granules are dried at 120 ℃ and prepared into samples.
Example 2:
10g of nano-sized alumina powder (average particle size: 320nm) and 6g of silane coupling agent KH570 were ultrasonically dispersed in toluene, reacted with stirring at 130 ℃ for 6 hours in a nitrogen atmosphere, and then cooled to room temperature. 12g of glycidyl methacrylate dissolved in toluene and a few drops of AIBN were added and the reaction was stirred at 80 ℃ for 2 hours under a nitrogen atmosphere. After centrifugal drying, acetone extraction is used for removing unreacted coupling agent and residual toluene solvent, finally drying is carried out, modified nanometer alumina particles are obtained, and the grafting rate of glycidyl methacrylate obtained by TGA data is 15.4 wt%.
Preheating 10g of modified nano-alumina particles at 90 ℃, adding the particles into 40g of PET polyester preheated and melted at 90 ℃, and stirring the particles for 3h in vacuum, wherein the number average molecular weight Mn of the PET polyester is 38500 daltons, so that the modified PET polyester is obtained by uniformly mixing the particles and the PET polyester.
70g of polycarbonate (the number average molecular weight Mn is 22000 dalton) and 30g of modified PET polyester are uniformly mixed, and then the mixture is added into a double-screw extruder to be extruded and granulated, wherein the extrusion processing temperature is controlled between 230 +/-2 ℃, and the screw rotating speed is 600 rpm. Then, the extruded and cut granules are dried at 110 ℃ and prepared into samples.
Example 3:
10g of nano-sized alumina powder (average particle size: 320nm) and 4g of silane coupling agent KH570 were ultrasonically dispersed in toluene, reacted with stirring at 125 ℃ for 3 hours in a nitrogen atmosphere, and then cooled to room temperature. 6g of glycidyl methacrylate dissolved in toluene and a few drops of AIBN were added and the reaction was stirred at 80 ℃ for 2 hours under a nitrogen atmosphere. After centrifugal drying, acetone extraction is used for removing unreacted coupling agent and residual toluene solvent, finally drying is carried out, modified nanometer alumina particles are obtained, and the grafting rate of glycidyl methacrylate obtained by TGA data is 11.3 wt%.
Preheating 7g of modified nano-alumina particles at 90 ℃, adding the modified nano-alumina particles into 42g of PET polyester preheated and melted at 90 ℃, stirring the PET polyester under vacuum for 4 hours to ensure that the modified PET polyester is uniformly mixed with the PET polyester, wherein the number average molecular weight Mn of the PET polyester is 38500 daltons.
60g of polycarbonate (the number average molecular weight Mn is 22000 dalton) and 40g of modified PET polyester are uniformly mixed, and then the mixture is added into a double-screw extruder to be extruded and granulated, wherein the extrusion processing temperature is controlled between 250 +/-2 ℃, and the rotation speed of the screw is 600 rpm. The extruded and cut pellets were then dried at 130 ℃ and prepared into samples.
Comparative example 1:
the remaining conditions were the same as in example 1, but unmodified nanosize alumina powder was used directly.
Comparative example 2:
the same procedure as in example 1 was repeated except that 10g of nanosized alumina powder (average particle diameter: 320nm), 1g of silane coupling agent KH570 and 2g of glycidyl methacrylate were used to obtain modified nanosized alumina particles having a glycidyl methacrylate graft ratio of 6.9 wt%.
Comparative example 3:
the same procedure as in example 1 was repeated except that 10g of nano-alumina (average particle diameter: 320nm), 0.5g of KH570 as a silane coupling agent, and 1g of glycidyl methacrylate were used to obtain modified nano-alumina particles having a glycidyl methacrylate graft ratio of 3.7 wt%.
The notched impact strength and elongation at break of the test specimens of examples 1-3 and comparative examples 1-3 according to the test methods described above are shown in Table 1 with the results associated therewith:
TABLE 1
Figure BDA0002220834320000081
As can be seen from Table 1, the materials obtained by using the modified PET polyester obtained by blending and modifying the modified nanoscale alumina particles of examples 1-3 of the invention and polycarbonate not only have higher impact strength, but also have higher elongation at break. Correlation index (notch impact strength is more than or equal to 50KJ m)-2And the elongation at break is more than or equal to 130 percent) so that the performance requirements of the automobile guide ball pin can be fully met.
The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention shall fall within the protection scope of the present invention.

Claims (10)

1. PET polyester is obtained by blending and modifying PET polyester and alumina particles; characterized in that the alumina particles are nano-scale alumina particles.
2. The PET polyester according to claim 1, wherein the number average molecular weight Mn of the PET polyester is 30000 and 46000 daltons.
3. The PET polyester of claim 1, wherein the nano-sized alumina particles are further modified from glycidyl methacrylate.
4. The PET polyester of claim 1, wherein the nano-sized alumina particles have a glycidyl methacrylate grafting ratio of 8.0-18.0%.
5. The PET polyester of claim 1, wherein the nano-sized alumina particles have a glycidyl methacrylate grafting ratio of 11.3-15.4%.
6. The PET polyester of claim 1, wherein the nano-sized alumina particles are obtained by reacting nano-sized alumina powder with a silane coupling agent and then polymerizing with glycidyl methacrylate.
7. The PET polyester of claim 6, wherein the weight ratio of nanoscale alumina powder, silane coupling agent, and glycidyl methacrylate is 10: (3-9): (4-15).
8. The PET polyester according to claim 6, wherein the silane coupling agent is a silane coupling agent having methacryloxypropyl groups.
9. The PET polyester of claim 1, wherein the weight ratio of the nano-sized alumina particles to the PET polyester is 1: (2-8).
10. An automobile guide ball pin made of a material formed by melt blending a polycarbonate and the PET polyester according to any one of claims 1 to 9.
CN201910933152.XA 2019-09-29 2019-09-29 Nano alumina particle modified PET polyester and formed automobile guide ball pin Active CN110684324B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910933152.XA CN110684324B (en) 2019-09-29 2019-09-29 Nano alumina particle modified PET polyester and formed automobile guide ball pin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910933152.XA CN110684324B (en) 2019-09-29 2019-09-29 Nano alumina particle modified PET polyester and formed automobile guide ball pin

Publications (2)

Publication Number Publication Date
CN110684324A true CN110684324A (en) 2020-01-14
CN110684324B CN110684324B (en) 2022-05-31

Family

ID=69110919

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910933152.XA Active CN110684324B (en) 2019-09-29 2019-09-29 Nano alumina particle modified PET polyester and formed automobile guide ball pin

Country Status (1)

Country Link
CN (1) CN110684324B (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN201280156Y (en) * 2008-10-16 2009-07-29 沈百庆 Guide ball-pin assembly
CN104693764A (en) * 2013-12-10 2015-06-10 青岛同创节能环保工程有限公司 Nano-particle filled and reinforced PC/PET alloy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN201280156Y (en) * 2008-10-16 2009-07-29 沈百庆 Guide ball-pin assembly
CN104693764A (en) * 2013-12-10 2015-06-10 青岛同创节能环保工程有限公司 Nano-particle filled and reinforced PC/PET alloy

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
唐荣芝等: "导热PET绝缘背板对光伏组件发电效率的影响", 《绝缘材料》 *
孙贵生等: "纳米二氧化硅表面改性及辐射引发接枝GMA的研究", 《辐射研究与辐射工艺学报》 *
王国全: "《聚合物共混改性原理与应用》", 31 January 2007, 中国轻工业出版社 *

Also Published As

Publication number Publication date
CN110684324B (en) 2022-05-31

Similar Documents

Publication Publication Date Title
CN101249410B (en) Preparation of organic-inorganic composite microballoons
US20090176924A1 (en) Pulverulent composition based on carbon nanotubes, methods of obtaining them and its uses, especially in polymeric materials
CN112538219A (en) Polypropylene composition and preparation method thereof
CN113321869A (en) Scratch-resistant easy-spraying polypropylene composite material and preparation method and application thereof
CN110628095A (en) Graphene high-elasticity rubber elastomer high polymer material and preparation method thereof
WO2022036954A1 (en) Antiviral automobile entertainment panel pc/abs alloy material and preparation method therefor
CN109705569B (en) Conductive polyphenyl ether/polyamide alloy with low linear expansion coefficient and preparation method thereof
CN110684324B (en) Nano alumina particle modified PET polyester and formed automobile guide ball pin
CN104017346A (en) Method for preparing high-ductility polymer blend alloy by melt blending
CN110669325B (en) Automobile guide ball pin formed by PET polyester modified by nano-alumina particles
CN110628198B (en) Method for preparing ball seat material for automobile guide ball pin
CN110607061B (en) Ball seat material for automobile guide ball pin and application thereof
CN110591324B (en) Ball seat material for automobile guide ball pin
CN115867605A (en) High performance materials comprising polymers and hybrid nano-additives
CN113789028A (en) Thermoplastic elastomer and preparation method thereof, application and regenerated and recycled ABS plastic and preparation method thereof
CN110684325B (en) Method for preparing ball seat material for automobile guide ball pin
CN1435437A (en) Process for preparing graft polyolefin/lamellar silicate composite nanomaterial
CN105131511A (en) Low-temperature toughened polyformaldehyde composite material and preparing method thereof
CN111333986B (en) PMMA/UHMWPE alloy material with chemical solvent resistance, high wear resistance and self-lubrication and preparation method thereof
CN100365076C (en) Nano carbon black with in-situ grafted organic compound and its producing method
CN109456586B (en) Melt blending method modified carbon nano particle/polycarbonate nano composite film and preparation method thereof
CN116675936A (en) Wear-resistant plastic with ageing resistance
CN107312304B (en) Two-dimensional reinforced polycarbonate composite material and preparation method thereof
CN114752176B (en) Spraying-free resin and preparation method and application thereof
CN104650293A (en) Preparation method for high-dispersion graphene in-situ modified petroleum resin

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