Nothing Special   »   [go: up one dir, main page]

CN101302338A - High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof - Google Patents

High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof Download PDF

Info

Publication number
CN101302338A
CN101302338A CNA2008100673453A CN200810067345A CN101302338A CN 101302338 A CN101302338 A CN 101302338A CN A2008100673453 A CNA2008100673453 A CN A2008100673453A CN 200810067345 A CN200810067345 A CN 200810067345A CN 101302338 A CN101302338 A CN 101302338A
Authority
CN
China
Prior art keywords
wear
temperature
district
polyamide material
percent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CNA2008100673453A
Other languages
Chinese (zh)
Inventor
徐东
贺永
王贤文
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.)
Polymer Science Shenzhen New Materials Co Ltd
Original Assignee
Polymer Science Shenzhen New Materials 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 Polymer Science Shenzhen New Materials Co Ltd filed Critical Polymer Science Shenzhen New Materials Co Ltd
Priority to CNA2008100673453A priority Critical patent/CN101302338A/en
Publication of CN101302338A publication Critical patent/CN101302338A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/918Thermal treatment of the stream of extruded material, e.g. cooling characterized by differential heating or cooling
    • B29C48/9185Thermal treatment of the stream of extruded material, e.g. cooling characterized by differential heating or cooling in the direction of the stream of the material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/04Particle-shaped
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/92Measuring, controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92504Controlled parameter
    • B29C2948/92704Temperature
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92819Location or phase of control
    • B29C2948/92857Extrusion unit
    • B29C2948/92876Feeding, melting, plasticising or pumping zones, e.g. the melt itself
    • B29C2948/92895Barrel or housing

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention discloses a polyamide material with high tenacity, wear-resisting capacity and self-lubricating property and a method for preparing the same. The compositions by weight percentage of the polyamide material are: 65 to 80 percent of polyhexamethylene adipamide, 15 to 23 percent of wear-resistant agent, 0 to 0.5 percent of lubricating agent, 0 to 3 percent of coupling agent, 0 to 0.5 percent of antioxidant, and 5 to 10 percent of toughener. The method improves wear-resisting property and self-lubricating property of the product mainly through auxiliary materials, thereby enlarging the application range of polyamide modified engineering plastics. The product of the invention has the advantages of good toughness, high impact strength, good surface glossiness, excellent chemical resistance and good dimension stability; a part of wear-resisting agent is added in the polyamide material, so the wear-resisting property of the material can be greatly improved; because the application range of the polyamide material is enlarged, wear-resisting requirements of partial transmission parts, shuttle wear parts and anti-sand-scraping parts can be met; and the polyamide material can be widely used for transmission components of an engine, an outer housing of a roller, an outer housing of an engine, a mechanical socket connector and transmission accessories, and can be used in positions which are often contacted and abraded in other transmission devices.

Description

A kind of high-toughness wear-resistant and self lubricity polyamide material and preparation method thereof
Technical field
The present invention relates to a kind of high molecule plastic technical field, relate in particular to the lubricated wear-resisting modified engineered plastic and preparation method thereof that reaches of a kind of hexamethylene diamine adipate.
Background technology
The hexamethylene diamine adipate resin is the universal very widely plastics of a kind of application, it has favorable rigidity, shock strength height, low temperature resistant, chemical proofing, physical strength and electric property are good, heat-resisting, surface hardness is high, and the characteristics of good dimension stability, finish size stability and surface luster are good, are used for the article component of the heat-resisting and product surface good luster of part.Make simultaneously the have specific characteristics engineering plastics of energy such as glass enhancings, fiberglass reinforced fire retardant easily.This series products is at electronic apparatus, widespread uses such as IT, household electrical appliances, automobile, toy, mechanical fitting.But its some shortcoming is low as the hexamethylene diamine adipate mechanical strength of resin of enhancing modified not, and water-absorbent is strong, and heat-resisting not high, toughness is bad etc., and therefore modification on the basis of hexamethylene diamine adipate resin can be satisfied the more demand of conglomerate.
The hexamethylene diamine adipate resin also more bad phenomenon can occur in the formed product process, do not reach as the not enough gloss of product surface, toughness of products, be easy to generate phenomenon of rupture, the product low-temperature flexibility is bad, product is easy peeling in rubbing for a long time and moving back and forth, wearing and tearing, phenomenons such as surface whiting.
Summary of the invention
The technical problem to be solved in the present invention provides a kind of high tenacity, wear resistance and self lubricity polyamide material.
The preparation method of this kind high tenacity, wear resistance and self lubricity polyamide material also will be provided simultaneously.
For solving the problems of the technologies described above, the present invention by the following technical solutions: a kind of high tenacity, wear resistance and self lubricity polyamide material, it is prepared from by following component: hexamethylene diamine adipate: 65-80%; Anti-wear agent: 15~23%; Lubricant: 0~0.5%; Coupling agent: 0~3%; Oxidation inhibitor: 0~0.5%; Toughner: 0-10%;
Above percentage ratio is weight percent.
Wherein, described hexamethylene diamine adipate is the virgin resin of viscosity between 2.5-2.8.Described antioxidant is phenolic antioxidant four [β-(3 ', 5 '-di-t-butyl-4 '-hydroxy phenyl) propionic acid] pentaerythritol ester and phosphite ester kind antioxidant (2,4 di-tert-butyl-phenyl) tris phosphite.Described toughner is that polyvinyl-maleic anhydride connects the branched copolymer material.Described lubrication prescription is hard ester acids or fatty acid.Described anti-wear agent is a kind of in molybdenumdisulphide or the tetrafluoroethylene.Described coupling agent is a kind of among commercially available KH550, the KH560.
The preparation method's of high-toughness wear-resistant of the present invention and self lubricity polyamide material technical scheme may further comprise the steps:
Step 1: take by weighing each component by above-mentioned weight percent;
Step 2: with the hexamethylene diamine adipate resin is matrix, mixes 4-6 minute in agitation vat after adding toughner, anti-wear agent, lubrication prescription, coupling agent, oxidation inhibitor and an amount of dispersant; Rotating speed is 500-1200 rev/min of worker;
Step 3: each component that will mix places twin screw extruder, through the melting mixing extruding pelletization, its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Advantage of the present invention is that to have improved hexamethylene diamine adipate material impact intensity low, and the defective of poor toughness the invention has the beneficial effects as follows: the good toughness of product, shock strength height, product are difficult for producing fracture.The intensity height, chemical resistant properties is good, dimensional stability good, the wear resisting property excellence, and surface gloss is good.Mainly be that the self lubricity of product is greatly improved owing to added anti-wear agent and coupling agent, the product surface glossiness is significantly increased, material is significantly improved in wear resistance, can use at the transmission product, come and go the wearing and tearing product, scratch resistance sand product etc. has the product of wear-resistant requirement.
Embodiment
In following examples of the present invention, the hexamethylene diamine adipate resin viscosity is 2.5-2.8, and main manufacturer is refreshing horse, Asahi Chemical Industry, first promise, Asia, sieve ground etc.; Toughner is that polyvinyl-maleic anhydride connects the branched copolymer material, and producer has Du Pont, Bai Chen, section logical etc.; Anti-wear agent is a kind of in molybdenumdisulphide or the tetrafluoroethylene, and there is big capital etc. in producer.Lubrication prescription is hard ester acids or fatty acid material; Coupling agent is organo silane coupling agent KH550.Oxidation inhibitor comprises phenolic antioxidant four [β-(3 ', 5 '-di-t-butyl-4 '-hydroxy phenyl) propionic acid] pentaerythritol ester and phosphite ester kind antioxidant (2,4 di-tert-butyl-phenyl) tris phosphite.
Embodiment 1
With resin hexamethylene diamine adipate weight resin ratio be: 78.1%; The anti-wear agent weight ratio is: 15%; The lubrication prescription weight ratio is: 0.2%; The coupling agent weight ratio is: 1.5%; The oxidation inhibitor weight ratio is: 0.2%; The toughner weight ratio is: 5%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Embodiment 2
With resin hexamethylene diamine adipate weight resin ratio be: 66%; The anti-wear agent weight ratio is: 20%; The lubrication prescription weight ratio is: 0.5%; The coupling agent weight ratio is: 3%; The oxidation inhibitor weight ratio is: 0.5%; The toughner weight ratio is: 10%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Embodiment 3
With resin hexamethylene diamine adipate weight resin ratio be: 71.4%; The anti-wear agent weight ratio is: 18%; The lubrication prescription weight ratio is: 0.3%; The coupling agent weight ratio is: 2%; The oxidation inhibitor weight ratio is: 0.3%; The toughner weight ratio is: 8%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Embodiment 4
With resin hexamethylene diamine adipate weight resin ratio be: 79.4%; The anti-wear agent weight ratio is: 18%; The lubrication prescription weight ratio is: 0.3%; The coupling agent weight ratio is: 2%; The oxidation inhibitor weight ratio is: 0.3%; The toughner weight ratio is: 0%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Embodiment 5
With resin hexamethylene diamine adipate weight resin ratio be: 74%; The anti-wear agent weight ratio is: 18%; The lubrication prescription weight ratio is: 0%; The coupling agent weight ratio is: 0%; The oxidation inhibitor weight ratio is: 0%; The toughner weight ratio is: 8%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Comparative Examples 1
With resin hexamethylene diamine adipate weight resin ratio be: 98.1%; The anti-wear agent weight ratio is: 0%; The lubrication prescription weight ratio is: 0.2%; The coupling agent weight ratio is: 1.5%; The oxidation inhibitor weight ratio is: 0.2%; The toughner weight ratio is: 0%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Comparative Examples 2
With resin hexamethylene diamine adipate weight resin ratio be: 90.1%; The anti-wear agent weight ratio is: 18%; The lubrication prescription weight ratio is: 0.2%; The coupling agent weight ratio is: 1.5%; The oxidation inhibitor weight ratio is: 0.2%; The toughner weight ratio is: 0%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Comparative Examples 3
With resin hexamethylene diamine adipate weight resin ratio be: 88.1%; The anti-wear agent weight ratio is: 0%; The lubrication prescription weight ratio is: 0.2%; The coupling agent weight ratio is: 1.5%; The oxidation inhibitor weight ratio is: 0.2%; The toughner weight ratio is: 10%; Above percentage ratio is weight percent.In high-speed mixer, mixed 4 minutes;
Each component that mixes places twin screw extruder, through the melting mixing extruding pelletization;
Its processing temperature is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, and three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃, engine speed: 300-350rpm.
Performance evaluation mode and implementation standard:
With the particle finished as stated above in 90~110 ℃ convection oven dry 4 hours in advance, and then the particulate material that drying is good carries out the injection molding sample preparation on injector, the injection mold temperature control is at 90 ℃, and the injection moulding temperature is controlled at 250-270 ℃.
The tensile property test is undertaken by ISO 527-2, and specimen size is 150*10*4, and draw speed is 50mm/min; The bending property test is undertaken by ISO 178, and specimen size is 80*10*4, and draw speed is 2mm/min, and span is 64mm, and simple beam impact strength is undertaken by ISO 179, and specimen size is 55*6*4, and notch depth is 1/3rd of a sample thickness; The test of ash is undertaken by the testing method of ISO 3451.
Comprehensive mechanical performance is passed judgment on by the numerical value of tensile strength, elongation at break, flexural strength, modulus in flexure, shock strength and the flame retardant resistance of test gained.
Table 1: the prescription transitivity table of embodiment 1-6
The matrix material title Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4 Embodiment 5
PA66 78.1 66 71.4 79.4 74
Anti-wear agent 15 20 18 18 18
Lubrication prescription 0.2 0.5 0.3 0.3 0
Coupling agent 1.5 3 2 2 0
Oxidation inhibitor 0.2 0.5 0.3 0.3 0
Toughner 5 10 8 0 8
Proportion 1.12 1.11 1.12 1.12 1.12
Flexural strength (Mpa) 89 81 85 89 76
Modulus in flexure (Mpa) 2120 1890 2050 2070 1750
Notched Izod impact strength (KJ/M2) 18 25 22 14.5 18
Tensile strength 59 54 57 58 49
(Mpa)
Fracture percentage of elongation (%) 21 32 30 25 28
Mobile (g/10min) 115 85 90 135 72
The product processing temperature (℃) 250-280 250-280 250-280 250-280 250-280
The injection moulding temperature (℃) 250-270 250-270 250-270 250-270 250-270
The prescription transitivity table of table 2: Comparative Examples 1-3
The matrix material title Comparative Examples 1 Comparative Examples 2 Comparative Examples 3
PA66 98.1 90.1 88.1
Anti-wear agent 0 18 0
Lubrication prescription 0.2 0.2 0.2
Coupling agent 1.5 1.5 1.5
Oxidation inhibitor 0.2 0.2 0.2
Toughner 0 0 10
Proportion 1.15 1.13 1.09
Flexural strength (Mpa) 93 91 76
Modulus in flexure (Mpa) 2300 2100 1650
Notched Izod impact strength (KJ/M2) 14 18 29
Tensile strength (Mpa) 62 58 45
Fracture percentage of elongation (%) 6 25 75
Mobile (g/10min) 150 80 45
The product processing temperature (℃) 250-280 250-280 250-280
The injection moulding temperature (℃) 250-270 250-270 240-260
From the performance of table 1 relatively, along with the increase of toughner ratio, the shock strength of material is significantly improved, but its flexural strength and tensile strength reduce, and the percentage of elongation of material obtains enlarging, and flowing property also significantly reduces.If do not add any lubrication prescription, oxidation inhibitor etc. in the material, the flowability of material is lower, causes the self lubricity of material on the low side, and the flowing property of material is bad, can bring a lot of difficulties in the injection moulding in later stage.If the toughner addition in the material is too much, the bending of material and tensile strength can descend significantly, and the insufficient strength height of material can not satisfy the requirement of strength of more products.See recently mutually with Comparative Examples with embodiment that again material does not add any toughner and anti-wear agent, the shock strength of material is obviously on the low side, can not reach some parts to the flexible requirement.Only add a spot of toughner or anti-wear agent, toughness, flowability and stretching, flexural strength to material all have tangible influence, for the over-all properties of balance strength, toughness and wear resistance, and the end-use of material, and the cost control of material, it is the most rational selecting embodiment 3 for use.

Claims (8)

1, a kind of high-toughness wear-resistant and self lubricity polyamide material, its composition is (%) by weight ratio:
PA 66 65-80%;
Anti-wear agent 15-23%;
Lubricant 0-0.5%;
Coupling agent 0-3%;
Oxidation inhibitor 0-0.5%;
Toughner 0-10%.
2, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material is characterized in that: described anti-wear agent is a kind of in molybdenumdisulphide or the tetrafluoroethylene.
3, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material is characterized in that: described toughner is that polyvinyl-maleic anhydride connects the branched copolymer material.
4, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material, it is characterized in that: described oxidation inhibitor comprises phenolic antioxidant four [β-(3 ', 5 '-di-t-butyl-4 '-hydroxy phenyl) propionic acid] pentaerythritol ester and phosphite ester kind antioxidant (2,4 di-tert-butyl-phenyl) tris phosphite.
5, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material is characterized in that: described lubricant is stearic acid and/or fatty acid.
6, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material is characterized in that: described coupling agent is a kind of among commercially available KH550, the KH560.
7, high-toughness wear-resistant according to claim 1 and self lubricity polyamide material is characterized in that: described hexamethylene diamine adipate resin is the virgin resin of viscosity at 2.5-2.8.
8, the preparation method of a kind of high-toughness wear-resistant as claimed in claim 1 and self lubricity polyamide material, it is characterized in that: this preparation method may further comprise the steps:
Step 1: take by weighing each component by above-mentioned weight percent;
Step 2: with the hexamethylene diamine adipate is matrix, adds toughner, anti-wear agent, lubrication prescription, coupling agent, oxidation inhibitor and mixes in high-speed mixer;
Step 3: each component that will mix places twin screw extruder, through the melting mixing extruding pelletization, its complete processing is district's temperature a: 240-250 ℃, two district's temperature: 245-260 ℃, three district's temperature: 245-260 ℃, four district's temperature: 250-270 ℃, five district's temperature: 250-280 ℃, six district's temperature: 250-275 ℃, seven district's temperature: 250-260 ℃.
CNA2008100673453A 2008-05-21 2008-05-21 High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof Pending CN101302338A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNA2008100673453A CN101302338A (en) 2008-05-21 2008-05-21 High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNA2008100673453A CN101302338A (en) 2008-05-21 2008-05-21 High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof

Publications (1)

Publication Number Publication Date
CN101302338A true CN101302338A (en) 2008-11-12

Family

ID=40112450

Family Applications (1)

Application Number Title Priority Date Filing Date
CNA2008100673453A Pending CN101302338A (en) 2008-05-21 2008-05-21 High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof

Country Status (1)

Country Link
CN (1) CN101302338A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101864168A (en) * 2010-07-12 2010-10-20 河南省科学院同位素研究所有限责任公司 Wear-resistant self-lubricating nylon compound material and method for preparing same
CN102051043A (en) * 2009-10-30 2011-05-11 上海金发科技发展有限公司 High wear-resistant and cold-resistant toughened nylon composite material
CN103360758A (en) * 2013-07-15 2013-10-23 上海秋橙新材料科技有限公司 Anti-aging PA-PTFE plastic alloy
CN103924323A (en) * 2014-04-29 2014-07-16 厦门怡龙谷新材料科技有限公司 Large-diameter composite monofilament with novel skin-core structure and preparation method and application of composite monofilament
CN104046009A (en) * 2014-06-20 2014-09-17 浙江衢州万能达科技有限公司 Nylon 6-polytetrafluoroethylene composition
CN104284771A (en) * 2012-05-09 2015-01-14 帝斯曼知识产权资产管理有限公司 Plastic engine cover
CN104403345A (en) * 2014-12-15 2015-03-11 苏州宽温电子科技有限公司 High-strength abrasion-proof high-molecular material and preparation method thereof
CN104419202A (en) * 2013-09-11 2015-03-18 安徽科聚新材料有限公司 Abrasion-resistant polytetrafluoroethylene and aramid fiber reinforced-modified PA66 material and preparation method thereof
CN105295356A (en) * 2014-06-09 2016-02-03 南通慧源塑胶有限公司 Formula of highly wear-resistant polyamide
CN106589919A (en) * 2015-10-19 2017-04-26 财团法人纺织产业综合研究所 Master batch of wear-resistant fiber, manufacturing method thereof and wear-resistant fiber manufactured by using master batch
CN113845722A (en) * 2021-09-28 2021-12-28 上海健康医学院 High-friction textile raw material and preparation method thereof

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102051043A (en) * 2009-10-30 2011-05-11 上海金发科技发展有限公司 High wear-resistant and cold-resistant toughened nylon composite material
CN102051043B (en) * 2009-10-30 2013-06-05 上海金发科技发展有限公司 High wear-resistant and cold-resistant toughened nylon composite material
CN101864168B (en) * 2010-07-12 2012-01-11 河南省科学院同位素研究所有限责任公司 Wear-resistant self-lubricating nylon compound material and method for preparing same
CN101864168A (en) * 2010-07-12 2010-10-20 河南省科学院同位素研究所有限责任公司 Wear-resistant self-lubricating nylon compound material and method for preparing same
US10266676B2 (en) 2012-05-09 2019-04-23 Dsm Ip Assets B.V. Plastic engine cover
CN104284771A (en) * 2012-05-09 2015-01-14 帝斯曼知识产权资产管理有限公司 Plastic engine cover
CN103360758A (en) * 2013-07-15 2013-10-23 上海秋橙新材料科技有限公司 Anti-aging PA-PTFE plastic alloy
CN103360758B (en) * 2013-07-15 2016-02-03 上海秋橙新材料科技有限公司 anti-aging PA-PTFE plastic alloy
CN104419202A (en) * 2013-09-11 2015-03-18 安徽科聚新材料有限公司 Abrasion-resistant polytetrafluoroethylene and aramid fiber reinforced-modified PA66 material and preparation method thereof
CN103924323A (en) * 2014-04-29 2014-07-16 厦门怡龙谷新材料科技有限公司 Large-diameter composite monofilament with novel skin-core structure and preparation method and application of composite monofilament
CN105295356A (en) * 2014-06-09 2016-02-03 南通慧源塑胶有限公司 Formula of highly wear-resistant polyamide
CN104046009A (en) * 2014-06-20 2014-09-17 浙江衢州万能达科技有限公司 Nylon 6-polytetrafluoroethylene composition
CN104403345A (en) * 2014-12-15 2015-03-11 苏州宽温电子科技有限公司 High-strength abrasion-proof high-molecular material and preparation method thereof
CN106589919A (en) * 2015-10-19 2017-04-26 财团法人纺织产业综合研究所 Master batch of wear-resistant fiber, manufacturing method thereof and wear-resistant fiber manufactured by using master batch
CN106589919B (en) * 2015-10-19 2019-11-05 财团法人纺织产业综合研究所 Master batch of wear-resistant fiber, manufacturing method thereof and wear-resistant fiber manufactured by using master batch
CN113845722A (en) * 2021-09-28 2021-12-28 上海健康医学院 High-friction textile raw material and preparation method thereof

Similar Documents

Publication Publication Date Title
CN101302338A (en) High-toughness, wear-resistant, self-lubricating polyamide material and preparation thereof
CN101311222B (en) High impact resistance fiberglass reinforced engineering plastics and preparation method
CN102585478B (en) Toughened polyphenyl ether and nylon alloy and preparation method for toughened polyphenyl ether and nylon alloy
CN101195707B (en) Glass fiber-reinforced nylon 6-polypropylene alloy material
CN101314672A (en) High-gloss, low-smell, reinforced nylon composite material and preparation method thereof
CN103059562B (en) High-glossiness anti-warping high-strength PA6 (polyamide 6) composite material, and preparation and application thereof
CN101302323B (en) Toughened and reinforced ABS material and preparation thereof
CN101205362A (en) Warpage-resistant composite reinforced nylon 66 composition
CN102876002A (en) Rapid molding high heat-resistant polyamide-polyphenyl ether alloy and preparation method thereof
CN103044910B (en) Glass fiber reinforced nylon 6 composite material with superhigh content and preparation method thereof
CN100549095C (en) Polyamide resin of a kind of halogen-free phosphor-free environmental protection inflaming retarding and preparation method thereof
CN110684337B (en) High-performance scratch-resistant polyamide/polyphenyl ether composite material and preparation method thereof
CN105504799B (en) Nylon composite materials
CN101220198A (en) Fiberglass reinforcing PBT alloy material and method for producing the same
CN102108209A (en) Warpage-resistant antistatic reinforced nylon 66 composite and preparation method thereof
CN101134838A (en) Glass fibre reinforced PC alloy material and method for preparing same
CN102485798A (en) Nylon composite material and preparation method thereof
CN101787182A (en) Method for preparing polybutylene terephthalate composite and mineral filler thereof
CN102863785A (en) Enhanced polyamide compound and preparation method thereof
CN1995124A (en) High tenacious polypropylene material for manufacturing central conditioner air-discharge hose and its preparation method
CN101104735B (en) High glazing and high liquidity glass fiber-reinforced nylon 6 composite material and preparation method thereof
CN113429781A (en) Long glass fiber reinforced bio-based polyamide 56, alloy and preparation method thereof
CN102942736B (en) High-glass fiber content reinforced polypropylene material and preparation method thereof
CN101440214A (en) Polyamide 6 composition for gas-assisted injection
CN104151580A (en) Preparation method of enhanced and toughened nylon PA66 modified engineering plastic

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication

Open date: 20081112