CN103483812B - A kind of preparation method of the wear resistant nylon 66 containing antioxidant - Google Patents

A kind of preparation method of the wear resistant nylon 66 containing antioxidant Download PDF

Info

Publication number
CN103483812B
CN103483812B CN201310411999.4A CN201310411999A CN103483812B CN 103483812 B CN103483812 B CN 103483812B CN 201310411999 A CN201310411999 A CN 201310411999A CN 103483812 B CN103483812 B CN 103483812B
Authority
CN
China
Prior art keywords
grams
antioxidant
wear resistant
resistant nylon
preparation
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
Application number
CN201310411999.4A
Other languages
Chinese (zh)
Other versions
CN103483812A (en
Inventor
沈国璋
程亚军
肖颖
付俊
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.)
Ningbo Jindi Engineering Plastic Co ltd
Ningbo Institute of Material Technology and Engineering of CAS
Original Assignee
Ningbo Jindi Engineering Plastic Co ltd
Ningbo Institute of Material Technology and Engineering of CAS
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 Ningbo Jindi Engineering Plastic Co ltd, Ningbo Institute of Material Technology and Engineering of CAS filed Critical Ningbo Jindi Engineering Plastic Co ltd
Priority to CN201310411999.4A priority Critical patent/CN103483812B/en
Publication of CN103483812A publication Critical patent/CN103483812A/en
Application granted granted Critical
Publication of CN103483812B publication Critical patent/CN103483812B/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
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
    • 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
    • C08K3/02Elements
    • C08K3/08Metals
    • 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
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/30Sulfur-, selenium- or tellurium-containing compounds
    • 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
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0881Titanium
    • 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
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • 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
    • C08K3/30Sulfur-, selenium- or tellurium-containing compounds
    • C08K2003/3009Sulfides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention relates to a kind of preparation method containing novel antioxidant wear resistant nylon PA66.By wear resistant nylon PA66? 100 parts, anti-wear agent molybdenumdisulphide 5 ~ 20 parts, anti-wear agent titanium dioxide 1 ~ 5 part, organic oxidation-resistant agent 0.1 ~ 1 part, after metal oxidation resistance agent titanium valve 0.1 ~ 1 part mixes, melt extrude preparation through twin screw and become wear resistant nylon PA66.Wear resistant nylon PA66 prepared by the inventive method has excellent wear resisting property and good mechanical property.

Description

A kind of preparation method of the wear resistant nylon 66 containing antioxidant
Technical field
The present invention relates to a kind of preparation method of wear resistant nylon 66, especially a kind of preparation method of the wear resistant nylon 66 containing novel antioxidant.
Background technology
Nylon66 fiber is a kind of very important engineering plastics, and mechanical property is excellent, and thermodynamics texturing temperature is high, and frictional coefficient is low, is widely used in all kinds of wear resistant appliance.In order to increase the wear resistance of nylon66 fiber further, main employing adds the frictional coefficient that inorganic wear resistant filler reduces material at present.The patent No. is the preparation method that the Chinese patent of CN102757641A provides a kind of high-ductility abrasion-proof nylon, and the anti-wear agent wherein used is graphite, one in silicon carbide or molybdenumdisulphide.Molybdenumdisulphide is a kind of cheap, and the anti-wear agent of excellent performance, can improve the wear resistance of nylon greatly.But molybdenumdisulphide is easily oxidized to the molybdic oxide crystal without wear resistance when high temperature.Because nylon66 fiber temperature in the course of processing is high, therefore molybdenumdisulphide easily lost efficacy, and caused the wear resisting property of nylon66 fiber to can not get significantly improving.Common organic antioxidant cannot stop molybdenumdisulphide deterioration by oxidation in the course of processing, therefore needs to find a kind of novel antioxidant and suppresses molybdenumdisulphide to be oxidized in high temperature working processes, at utmost improving the wear resistance of nylon66 fiber.
Summary of the invention
The object of the invention is for the deficiencies in the prior art, a kind of preparation method of the wear resistant nylon 66 containing novel antioxidant is provided.
The present invention to the effect that adopts metallic titanium powder jointly to use as antioxidant and traditional organic antioxidant, suppresses the oxidation of material.
The inventive method is specifically:
Step (1). weigh following raw material: parts by weight are the nylon66 fiber of 100 parts, the molybdenumdisulphide of 5 ~ 20 parts, the titanium dioxide of 1 ~ 5 part, the organic oxidation-resistant agent of 0.1 ~ 1 part, the metallic titanium powder of 0.1 ~ 1 part.
Described nylon66 fiber is common unmodified resin PA66, and fusing point is 255 ~ 265 DEG C;
Described molybdenumdisulphide is of a size of 1 ~ 10 micron, uses as anti-wear agent;
Described titanium dioxide is of a size of 50 ~ 200 nanometers, uses as anti-wear agent;
Described organic oxidation-resistant agent is one or more in antioxidant B215, antioxidant B225, antioxidant 1010, antioxidant 1076;
Described metallic titanium powder is of a size of 1 ~ 10 micron, uses as antioxidant.
Step (2). above-mentioned raw materials being joined rotating speed is mix 3 ~ 10 minutes in the high-speed mixer of 300 ~ 800rpm, obtains compound.
Step (3). above-mentioned compound is joined extruding pelletization in twin screw extruder; at the dicing machine pelletizing that is 300 ~ 800rpm of temperature be 15 ~ 40 DEG C tank water-cooled, rotating speed is placed on 70 ~ 110 DEG C, vacuum-drying 5 ~ 10 hours, obtains wear resistant nylon 66 particle.
The screw speed of described twin screw extruder is 80 ~ 250rpm, and in the course of processing, processing temperature is feeding section 240 ~ 260 DEG C, fluxing zone 260 ~ 280 DEG C, homogenizing zone 270 ~ 300 DEG C, head temperature 240 ~ 260 DEG C.
The inventive method adopts metallic titanium powder as composite antioxidant, effectively can suppress molybdenumdisulphide deterioration by oxidation in high temperature working processes.Standby wear resistant nylon 66 mechanical property of this legal system is excellent, and wear resistance is good, is prepared into long service life after device.
Embodiment
Below in conjunction with specific embodiment, the present invention is further analyzed.
Comparative example 1.
Step (1). weigh 1000 grams of nylon66 fiber, 150 grams of molybdenumdisulphide, 20 grams of titanium dioxide, 3 grams of antioxidant B225.
Step (2). above-mentioned raw materials being joined rotating speed is mix 10 minutes in the high-speed mixer of 300rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 100rpm; twin screw extruder processing temperature in the course of processing is feeding section 240 DEG C; fluxing zone 260 DEG C; homogenizing zone 270 DEG C; head temperature 240 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 400rpm, and vacuum-drying 10 hours at 80 DEG C, obtains wear resistant nylon 66 particle.
Wear resistant nylon 66 physicals prepared by table 1 comparative example 1.
Performance Testing standard Unit Numerical value
Tensile strength ASTM-D 638 MPa 124
Flexural strength ASTM-D 790 MPa 159
Modulus in flexure ASTM-D 791 MPa 6500
Frictional coefficient GB 3960-83 Kinetic friction 0.22
Wear resistant nylon 66 tensile strength prepared by comparative example 1 is 124MPa, and flexural strength is 159MPa, and modulus in flexure is 6500MPa, and kinetic friction coefficient is 0.22.
Embodiment 1.
Step (1). weigh 1000 grams of nylon66 fiber, 150 grams of molybdenumdisulphide, 20 grams of titanium dioxide, 3 grams of antioxidant B225,5 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 10 minutes in the high-speed mixer of 300rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 100rpm; twin screw extruder processing temperature in the course of processing is feeding section 240 DEG C; fluxing zone 260 DEG C; homogenizing zone 270 DEG C; head temperature 240 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 400rpm, and vacuum-drying 10 hours at 80 DEG C, obtains wear resistant nylon 66 particle.
Wear resistant nylon 66 excellent in mechanical performance prepared by embodiment 1, wear resistance is good, and wherein tensile strength is 153MPa, and flexural strength is 208MPa, and modulus in flexure is 7400MPa, and kinetic friction coefficient is 0.12.According to the contrast of comparative example 1 with embodiment 1, illustrate that the wear resistant nylon 66 sample mechanical property and wear resisting property of not adding titanium valve are all lower than wear resistant nylon 66 material prepared by the inventive method.
Wear resistant nylon 66 physicals prepared by table 2 embodiment 1.
Performance Testing standard Unit Numerical value
Tensile strength ASTM-D 638 MPa 153
Flexural strength ASTM-D 790 MPa 208
Modulus in flexure ASTM-D 791 MPa 7400
Frictional coefficient GB 3960-83 Kinetic friction 0.12
Embodiment 2.
Step (1). weigh 1000 grams of nylon66 fiber, 50 grams of molybdenumdisulphide, 50 grams of titanium dioxide, 10 grams of antioxidant B225,10 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 3 minutes in the high-speed mixer of 800rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 80rpm; twin screw extruder processing temperature in the course of processing is feeding section 260 DEG C; fluxing zone 280 DEG C; homogenizing zone 300 DEG C; head temperature 260 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 15 DEG C is after the dicing machine pelletizing of 300rpm, and vacuum-drying 5 hours at 70 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 3.
Step (1). weigh 1000 grams of nylon66 fiber, 200 grams of molybdenumdisulphide, 10 grams of titanium dioxide, 1g antioxidant B215,6 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 5 minutes in the high-speed mixer of 500rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 250rpm; twin screw extruder processing temperature in the course of processing is feeding section 250 DEG C; fluxing zone 270 DEG C; homogenizing zone 285 DEG C; head temperature 250 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 40 DEG C is after the dicing machine pelletizing of 800rpm, and vacuum-drying 6 hours at 110 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 4.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B215,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 120rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 290 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 7 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 5.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant 1010s, 2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 7 minutes in the high-speed mixer of 700rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 160rpm; twin screw extruder processing temperature in the course of processing is feeding section 245 DEG C; fluxing zone 265 DEG C; homogenizing zone 280 DEG C; head temperature 245 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 30 DEG C is after the dicing machine pelletizing of 700rpm, and vacuum-drying 8 hours at 110 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 6.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 220rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 280 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 650rpm, and vacuum-drying 9.5 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 7.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B215,3 grams of antioxidant B225,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in 200rpm twin screw extruder; twin screw extruder processing temperature in the course of processing is feeding section 250 DEG C; fluxing zone 270 DEG C; homogenizing zone 280 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 6 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 8.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 2 grams of antioxidant B215,2 grams of antioxidant 1010s, 2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 6 minutes in the high-speed mixer of 700rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 210rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 290 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 500rpm, and vacuum-drying 7 hours at 75 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 9.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B215,5 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 190rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 300 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 8 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 10.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B225,1 gram of antioxidant 1010,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 230rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 280 DEG C; head temperature 255 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 9 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 11.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 5 grams of antioxidant B225,5 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 9 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 170rpm; twin screw extruder processing temperature in the course of processing is feeding section 250 DEG C; fluxing zone 265 DEG C; homogenizing zone 290 DEG C; head temperature 260 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 5.5 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 12.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 4 grams of antioxidant 1010s, 2 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). be extruding pelletization in the twin screw extruder of 150rpm at screw speed by above-mentioned compound; twin screw extruder processing temperature in the course of processing is feeding section 240 DEG C; fluxing zone 260 DEG C; homogenizing zone 275 DEG C; head temperature 245 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 8 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 13.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B215,3 grams of antioxidant B225,3 grams of antioxidant 1010s, 2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 130rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 265 DEG C; homogenizing zone 295 DEG C; head temperature 240 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 35 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 8 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 14.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 2 grams of antioxidant B215,1 gram of antioxidant 1010,3 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 160rpm; twin screw extruder processing temperature in the course of processing is feeding section 255 DEG C; fluxing zone 275 DEG C; homogenizing zone 280 DEG C; head temperature 260 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 8 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 15.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 3 grams of antioxidant B225,3 grams of antioxidant 1010s, 4 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 250rpm; twin screw extruder processing temperature in the course of processing is feeding section 245 DEG C; fluxing zone 275 DEG C; homogenizing zone 290 DEG C; head temperature 245 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 6.5 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 16.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 30 grams of titanium dioxide, 1 gram of antioxidant B215,1 gram of antioxidant B225,1 gram of antioxidant, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 600rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 100rpm; twin screw extruder processing temperature in the course of processing is feeding section 260 DEG C; fluxing zone 270 DEG C; homogenizing zone 280 DEG C; head temperature 250 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 8 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 17.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 35 grams of titanium dioxide, 3 grams of antioxidant B215,2 grams of antioxidant B225,2 grams of antioxidant 1010s, 2 grams of antioxidants, 1076,2 grams of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 650rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 80rpm; twin screw extruder processing temperature in the course of processing is feeding section 240 DEG C; fluxing zone 280 DEG C; homogenizing zone 300 DEG C; head temperature 260 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 10 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
Embodiment 18.
Step (1). weigh 1000 grams of nylon66 fiber, 100 grams of molybdenumdisulphide, 50 grams of titanium dioxide, 1 gram of antioxidant, 1076,1 gram of metallic titanium powder.
Step (2). above-mentioned raw materials being joined rotating speed is mix 8 minutes in the high-speed mixer of 650rpm, obtains compound.
Step (3). above-mentioned compound being joined screw speed is extruding pelletization in the twin screw extruder of 200rpm; twin screw extruder processing temperature in the course of processing is feeding section 240 DEG C; fluxing zone 280 DEG C; homogenizing zone 300 DEG C; head temperature 260 DEG C; then to be placed in temperature be tank water-cooled, the rotating speed of 25 DEG C is after the dicing machine pelletizing of 600rpm, and vacuum-drying 10 hours at 100 DEG C, obtains wear resistant nylon 66 particle.
The nylon66 fiber used in above-mentioned all embodiments is common unmodified resin PA66, and fusing point is 255 ~ 265 DEG C; Molybdenumdisulphide is of a size of 1 ~ 10 micron; Titanium dioxide is of a size of 50 ~ 200 nanometers; Metallic titanium powder is of a size of 1 ~ 10 micron.
Above-described embodiment is not that the present invention is not limited only to above-described embodiment for restriction of the present invention, as long as meet application claims, all belongs to protection scope of the present invention.

Claims (7)

1. a preparation method for the wear resistant nylon 66 containing antioxidant, is characterized in that the method comprises the following steps:
Step (1). weigh following raw material: parts by weight are the nylon66 fiber of 100 parts, the molybdenumdisulphide of 5 ~ 20 parts, the titanium dioxide of 1 ~ 5 part, the organic oxidation-resistant agent of 0.1 ~ 1 part, the metallic titanium powder of 0.1 ~ 1 part;
Step (2). above-mentioned raw materials being joined rotating speed is mix 3 ~ 10 minutes in the high-speed mixer of 300 ~ 800rpm, obtains compound;
Step (3). above-mentioned compound is joined extruding pelletization in twin screw extruder; at the dicing machine pelletizing that is 300 ~ 800rpm of temperature be 15 ~ 40 DEG C tank water-cooled, rotating speed is placed on 70 ~ 110 DEG C, vacuum-drying 5 ~ 10 hours, obtains wear resistant nylon 66 particle.
2. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, it is characterized in that described nylon66 fiber is common unmodified resin PA66, fusing point is 255 ~ 265 DEG C.
3. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, is characterized in that described molybdenumdisulphide is of a size of 1 ~ 10 micron, uses as anti-wear agent.
4. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, is characterized in that described titanium dioxide is of a size of 50 ~ 200 nanometers, uses as anti-wear agent.
5. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, is characterized in that described organic oxidation-resistant agent is one or more in antioxidant B215, antioxidant B225, antioxidant 1010, antioxidant 1076.
6. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, is characterized in that described metallic titanium powder is of a size of 1 ~ 10 micron, uses as antioxidant.
7. the preparation method of a kind of wear resistant nylon 66 containing antioxidant as claimed in claim 1, it is characterized in that the screw speed of described twin screw extruder is 80 ~ 250rpm, in the course of processing, processing temperature is feeding section 240 ~ 260 DEG C, fluxing zone 260 ~ 280 DEG C, homogenizing zone 270 ~ 300 DEG C, head temperature 240 ~ 260 DEG C.
CN201310411999.4A 2013-09-11 2013-09-11 A kind of preparation method of the wear resistant nylon 66 containing antioxidant Active CN103483812B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310411999.4A CN103483812B (en) 2013-09-11 2013-09-11 A kind of preparation method of the wear resistant nylon 66 containing antioxidant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310411999.4A CN103483812B (en) 2013-09-11 2013-09-11 A kind of preparation method of the wear resistant nylon 66 containing antioxidant

Publications (2)

Publication Number Publication Date
CN103483812A CN103483812A (en) 2014-01-01
CN103483812B true CN103483812B (en) 2015-12-02

Family

ID=49824433

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310411999.4A Active CN103483812B (en) 2013-09-11 2013-09-11 A kind of preparation method of the wear resistant nylon 66 containing antioxidant

Country Status (1)

Country Link
CN (1) CN103483812B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114990729A (en) * 2022-06-15 2022-09-02 广州明晖新材料有限公司 Wear-resistant nylon yarn and preparation method thereof
CN115537021B (en) * 2022-11-02 2023-09-29 苏州和庚丽塑胶科技有限公司 Modified nylon 66 particles and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101838576A (en) * 2009-03-20 2010-09-22 中国科学院宁波材料技术与工程研究所 Dry film lubricant based on modified epoxy resin and preparation method thereof
CN102757641A (en) * 2012-08-10 2012-10-31 平顶山亚塑工业有限公司 High toughness and wear resistant nylon and preparation method thereof
CN102787003A (en) * 2012-09-03 2012-11-21 通化七星润滑油制造有限责任公司 Compound lubricating grease and preparation method of compound lubricating grease

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101838576A (en) * 2009-03-20 2010-09-22 中国科学院宁波材料技术与工程研究所 Dry film lubricant based on modified epoxy resin and preparation method thereof
CN102757641A (en) * 2012-08-10 2012-10-31 平顶山亚塑工业有限公司 High toughness and wear resistant nylon and preparation method thereof
CN102787003A (en) * 2012-09-03 2012-11-21 通化七星润滑油制造有限责任公司 Compound lubricating grease and preparation method of compound lubricating grease

Also Published As

Publication number Publication date
CN103483812A (en) 2014-01-01

Similar Documents

Publication Publication Date Title
CN102786797B (en) Multiscale carbon fiber nylon composite material and preparation method thereof
CN102417640B (en) Production formula of high-temperature high-speed high-wear resistant spinning rubber roll
CN103483812B (en) A kind of preparation method of the wear resistant nylon 66 containing antioxidant
CN103724767A (en) Anti-aging fishing net
CN103409687A (en) Powder metallurgy supporting seat and preparation method thereof
CN110184546B (en) Heavy-load powder metallurgy oil-retaining bearing and preparation method thereof
CN103613902A (en) Heat-conducting friction-resistant polyformaldehyde composite material and preparation method thereof
CN101800089B (en) Nanometer NbSe2 copper-base solid self-lubricating composite material and preparation method thereof
WO2014185291A1 (en) Ptfe resin composition
CN103102598A (en) High-temperature resistant steel wire rope core conveying belt core glue and preparation method thereof
CN103483810B (en) A kind of preparation method of the wear resistant nylon 6 containing novel antioxidant
CN103788491A (en) Reaction type continuous long glass fiber reinforced polypropylene compound and preparation method thereof
CN101824219B (en) Amorphous metal enhanced polyphenylene sulfide self-lubricating wear-resistant composite material
CN103483813B (en) A kind of preparation method of the wear resistant nylon 1010 containing antioxidant
CN105111693A (en) Carbon nano composite fiber material and preparation method thereof
CN104277259A (en) Wear-resistant rubber pad
CN103613903A (en) Friction-resistant composite material and preparation method thereof
CN109503905A (en) A kind of high-lubricity rubber ring
CN102506107A (en) Wet type friction clutch disc material for transmitting high power and preparation process
CN102786796A (en) TPU (Thermoplastic Urethane) modified carbon fiber/nylon composite material and preparation method thereof
CN103788629A (en) Highly wear-resistant low-noise glass fiber reinforced nylon composite material composition and preparation method thereof
CN103589149B (en) Composite for supporting roller bearing seat and preparation method thereof
CN103275375B (en) A kind of ultrahigh molecular weight polyethylene(UHMWPE) thermospray PP Pipe Compound and preparation method thereof
CN102359522B (en) Brake friction plate and preparation method thereof
CN105924825A (en) Chemical attack resisting PVC cable material

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant