CN106222474A - A kind of preparation method of silver molybdenum sulfide sliding contact material - Google Patents

A kind of preparation method of silver molybdenum sulfide sliding contact material Download PDF

Info

Publication number
CN106222474A
CN106222474A CN201610742307.8A CN201610742307A CN106222474A CN 106222474 A CN106222474 A CN 106222474A CN 201610742307 A CN201610742307 A CN 201610742307A CN 106222474 A CN106222474 A CN 106222474A
Authority
CN
China
Prior art keywords
sliding contact
contact material
silver
molybdenum sulfide
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.)
Granted
Application number
CN201610742307.8A
Other languages
Chinese (zh)
Other versions
CN106222474B (en
Inventor
周晓龙
周兆波
曹建春
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.)
Kunming University of Science and Technology
Original Assignee
Kunming University of Science and Technology
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 Kunming University of Science and Technology filed Critical Kunming University of Science and Technology
Priority to CN201610742307.8A priority Critical patent/CN106222474B/en
Publication of CN106222474A publication Critical patent/CN106222474A/en
Application granted granted Critical
Publication of CN106222474B publication Critical patent/CN106222474B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1005Pretreatment of the non-metallic additives
    • C22C1/1015Pretreatment of the non-metallic additives by preparing or treating a non-metallic additive preform
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • C22C1/1047Alloys containing non-metals starting from a melt by mixing and casting liquid metal matrix composites
    • C22C1/1052Alloys containing non-metals starting from a melt by mixing and casting liquid metal matrix composites by mixing and casting metal matrix composites with reaction
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0089Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with other, not previously mentioned inorganic compounds as the main non-metallic constituent, e.g. sulfides, glass
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C5/00Alloys based on noble metals
    • C22C5/06Alloys based on silver
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B13/00Apparatus or processes specially adapted for manufacturing conductors or cables

Abstract

The present invention discloses the preparation method of a kind of silver molybdenum sulfide sliding contact material, belongs to sliding contact material technical field.The method of the invention is by receiving the MoS of (micro-) grain of rice degree to having self-lubricating property2Powder body material carries out pelletize, it is thus achieved that the spherical particles of about 0.01mm~1.5mm, and this spherical particles epoxy bond is become differently shaped particle group, and then these differently shaped particles group is bonded in the inner surface of mould;Finally the silvering solution of fusing is poured in shaping dies, is uniform-distribution with hexagon or five deformation or the difform MoS with self-lubricating property such as circle preparing surface2The silver-based sliding contact material of particle swarm.The advantage of the method is that with short production cycle, technique is simple, and without wastage of material, be not required to mixed powder, be not required to the techniques such as extruding and drawing molding;And owing to using pouring technology, the silver-colored molybdenum sulfide sliding contact material prepared relative to currently used PM technique has the advantages such as conductivity, resistance to electrical wear are good.

Description

A kind of preparation method of silver molybdenum sulfide sliding contact material
Technical field
The present invention relates to the preparation method of a kind of silver molybdenum sulfide sliding contact material, use the method for melting and casting to prepare Surface distributed has the silver-based sliding contact material of self-lubricating granule molybdenum sulfide, belongs to sliding contact material technical field.
Background technology
Silver molybdenum sulfide (AgMoS2) composite be a kind of slip being widely used as in the space flight mechanisms such as satellite make electrical contact with material Material, Main Function is electrical power and the telemetered signal of Satellite vapour image to be delivered in satellite body.The quality of its performance Directly decide the stability of Circuits System, accuracy and life-span.
Conventional AgMoS2The technology of preparing of composite contact material mainly uses PM technique, its technique be by The Ag powder of certain particle size and MoS2After powder is sufficiently mixed, complete through several steps such as compacting, sintering, densifications.This technique Advantage be simple to operate, different MoS can be prepared according to actual needs2The AgMoS of content2Composite;Shortcoming is Ag and MoS2 Interface easily contaminated in preparation, interface cohesion is poor, and MoS2Granule skewness in silver matrix, causes AgMoS2Conductivity of composite material and the instability of wearability, have a strong impact on stability and the accuracy of Circuits System.
The present invention is directed to AgMoS prepared by powder metallurgy2The deficiency that known technology exists, it is proposed that a kind of by simple casting Make and obtain the AgMoS with self-lubricating property2Sliding contact material.
Summary of the invention
It is an object of the invention to provide a kind of silver molybdenum sulfide sliding contact material preparation method, specifically include following step Rapid: MoS2Powder body material carries out pelletize and is prepared as the spherical particles of a diameter of 0.01mm~1.5mm, then that this is the most spherical Granule is bonded to particle swarm, and this particle swarm is bonded on the inwall of shaping dies (holding between particle swarm and particle swarm The distance of 0.5mm~10mm), and the silvering solution of fusing is poured in shaping dies, finally preparing surface has MoS2Particle swarm Silver-colored molybdenum sulfide sliding contact material.
Preferably, MoS of the present invention2The granularity of powder body is 50nm-50um.
Preferably, particle swarm of the present invention can be circle, square, rectangle, pentagon, hexagon, linear type Pole shape, the particle swarm used in each preparation process can be one or more in these shapes;When using a kind of The silver-colored molybdenum sulfide sliding contact material surface prepared during grain group is only distributed the MoS of a kind of shape2Particle swarm, works as use The silver-colored molybdenum sulfide sliding contact material surface prepared during multiple particle swarm is only distributed the MoS of various shape2Particle swarm; Wherein circle, square, rectangle, pentagon, hexagonal thickness are 1.5mm-9mm;Linear type pole shape a diameter of 1.5mm-7.5mm.In addition to linear type pole shape particle swarm, the enclosed area of particle swarm of other shapes is not more than 80 square millimeters.
Preferably, it is epoxy resin that spheroidal particle is bonded to the binding agent used in particle swarm process.
Preferably, shaping dies of the present invention need to first pass through spray carbon process.
Preferably, melting and the pouring condition of described silver liquation of the present invention is: fusion temperature is 980-1100 DEG C, molten The silvering solution graphite powder changed or activated carbon powder cover, and pouring temperature is 970-1050 DEG C.
Beneficial effects of the present invention:
(1) traditional preparation AgMoS has been abandoned2Sliding contact material frequently with powder metallurgy process need pressed compact, sinter, squeeze The techniques such as pressure, drawing, shorten technological process.
(2) AgMoS relative to powder metallurgic method, prepared by the present invention2The consistency of sliding contact material is higher, tool There is good conductivity.
(3) AgMoS prepared by the present invention2Sliding contact material product and AgMoS in the market2Slide and make electrical contact with Material is compared, and has the advantage that organizational structure is adjustable, consistency is high, conductivity is good, wearability is good, thus has good city Field prospect.
Accompanying drawing explanation
Fig. 1 is differently shaped particle group.
Fig. 2 is the process chart of the present invention.
Specific embodiments
Below in conjunction with drawings and Examples, the present invention is further elaborated, but the protection content of the present invention is not limited to implement Scope described in example.
Embodiment 1
Such as the technological process of Fig. 2, by the MoS of 50nm granularity2Powder is a granulated into the spheroidal particle of 0.1mm, and is used by 0.1mm granule Epoxy bond becomes such as the hexagon (this hexagon area that particle swarm encloses is about 80 square millimeters) in Fig. 1, by 10 six It is hexagon MoS thick for 1mm that limit shape is bonded to thickness2Particle swarm;Then by multiple hexagon MoS2Particle swarm is bonded to through overspray The inwall of the casting mould that carbon processes, and make MoS2The distance of 10mm is kept between particle swarm and particle swarm;Finally 980 DEG C are melted The silvering solution (top layer activated carbon covers) changed is poured in casting mould the pouring temperatures of 970 DEG C and prepares MoS2Strengthen AgMoS2Sliding contact material.
Embodiment 2
Such as the technological process of Fig. 2, by the MoS of 800nm granularity2Powder is a granulated into the spheroidal particle of 0.01mm, and by 0.01mm granule Such as the square (this square area that particle swarm encloses is about 5 square millimeters) in Fig. 1 is become, by 50 just by epoxy bond The square thickness that is bonded to is square MoS thick for 0.5mm2Particle swarm;Then by multiple this square MoS2Particle swarm be bonded to through The inwall of the casting mould that overspray carbon processes, and make MoS2The distance of 2mm is kept between particle swarm and particle swarm;Finally by 1020 DEG C fusing silvering solution (top layer activated carbon covers) the pouring temperatures of 1000 DEG C be poured in casting mould prepare MoS2Strengthen AgMoS2Sliding contact material.
Embodiment 3
Such as the technological process of Fig. 2, the graphite powder of 50um granularity is a granulated into the spheroidal particle of 0.5mm, and by 0.5mm granule ring Epoxy resins be bonded to such as Fig. 1 in round bar shape, and make the MoS of pole2The diameter of particle swarm reaches 2mm;Then by multiple this The pole MoS of a diameter of 2mm2Particle swarm is bonded to the inwall of the casting mould processed through overspray carbon, and makes MoS2Particle swarm with The distance of 5mm is kept between particle swarm;Finally by 1100 DEG C of silvering solutions (top layer activated carbon covers) melted the cast of 1050 DEG C Temperature is poured in casting mould and prepares MoS2Strengthen AgMoS2Sliding contact material.

Claims (8)

1. a silver-colored molybdenum sulfide sliding contact material preparation method, it is characterised in that specifically include following steps: MoS2Powder body Material carries out pelletize and is prepared as the spherical particles of a diameter of 0.01mm~1.5mm, is the most then bonded to by this spheroidal particle Grain group, and this particle swarm is bonded on the inwall of shaping dies, and the silvering solution of fusing is poured in shaping dies, finally make MoS is had for going out surface2The silver-colored molybdenum sulfide sliding contact material of particle swarm.
Silver molybdenum sulfide sliding contact material preparation method the most according to claim 1, it is characterised in that: MoS2The grain of powder body Degree is 50nm-50um.
The preparation method of silver molybdenum sulfide sliding contact material the most according to claim 1, it is characterised in that: described granule The shape of group can be circle, square, rectangle, pentagon, hexagon, linear type pole shape;Wherein circular, square, Rectangle, pentagon, hexagonal thickness are 1.5mm-9mm;A diameter of 1.5mm-7.5mm of linear type pole shape.
The preparation method of silver molybdenum sulfide sliding contact material the most according to claim 1, it is characterised in that: except linear type Outside pole shape particle swarm, the enclosed area of particle swarm of other shapes is not more than 80 square millimeters.
The most according to claim 1 silver molybdenum sulfide sliding contact material preparation method, it is characterised in that: particle swarm with The distance of 0.5mm~10mm is kept between particle swarm.
The preparation method of silver molybdenum sulfide sliding contact material the most according to claim 1, it is characterised in that: by spherical It is epoxy resin that grain is bonded to the binding agent used in particle swarm process.
The preparation method of silver molybdenum sulfide sliding contact material the most according to claim 1, it is characterised in that: shaping dies First pass through spray carbon before using to process.
The preparation method of silver molybdenum sulfide sliding contact material the most according to claim 1, it is characterised in that: described silver melts The melting of liquid and pouring condition be: fusion temperature is 980-1100 DEG C, and the silvering solution graphite powder of fusing or activated carbon powder cover, and water Note temperature is 970-1050 DEG C.
CN201610742307.8A 2016-08-29 2016-08-29 A kind of preparation method of silver-colored molybdenum sulfide sliding contact material Active CN106222474B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610742307.8A CN106222474B (en) 2016-08-29 2016-08-29 A kind of preparation method of silver-colored molybdenum sulfide sliding contact material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610742307.8A CN106222474B (en) 2016-08-29 2016-08-29 A kind of preparation method of silver-colored molybdenum sulfide sliding contact material

Publications (2)

Publication Number Publication Date
CN106222474A true CN106222474A (en) 2016-12-14
CN106222474B CN106222474B (en) 2017-11-10

Family

ID=57556108

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610742307.8A Active CN106222474B (en) 2016-08-29 2016-08-29 A kind of preparation method of silver-colored molybdenum sulfide sliding contact material

Country Status (1)

Country Link
CN (1) CN106222474B (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030209103A1 (en) * 2002-05-10 2003-11-13 Komatsu Ltd. Cooper-based sintering sliding material and multi-layered sintered sliding member
JP2006037179A (en) * 2004-07-28 2006-02-09 Taiho Kogyo Co Ltd Pb-FREE COPPER-ALLOY-BASED COMPOSITE SLIDING MATERIAL SUPERIOR IN SEIZURE RESISTANCE
JP2006037180A (en) * 2004-07-28 2006-02-09 Taiho Kogyo Co Ltd COMPOSITE SLIDING MATERIAL SUPERIOR IN SEIZURE RESISTANCE MADE OF Pb-FREE COPPER ALLOY
CN101619406A (en) * 2009-07-24 2010-01-06 核工业理化工程研究院华核新技术开发公司 High-temperature nickel-based self-lubricating material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030209103A1 (en) * 2002-05-10 2003-11-13 Komatsu Ltd. Cooper-based sintering sliding material and multi-layered sintered sliding member
JP2006037179A (en) * 2004-07-28 2006-02-09 Taiho Kogyo Co Ltd Pb-FREE COPPER-ALLOY-BASED COMPOSITE SLIDING MATERIAL SUPERIOR IN SEIZURE RESISTANCE
JP2006037180A (en) * 2004-07-28 2006-02-09 Taiho Kogyo Co Ltd COMPOSITE SLIDING MATERIAL SUPERIOR IN SEIZURE RESISTANCE MADE OF Pb-FREE COPPER ALLOY
CN101619406A (en) * 2009-07-24 2010-01-06 核工业理化工程研究院华核新技术开发公司 High-temperature nickel-based self-lubricating material and preparation method thereof

Also Published As

Publication number Publication date
CN106222474B (en) 2017-11-10

Similar Documents

Publication Publication Date Title
CN105256168B (en) Copper-based graphite self-lubricating composite material and preparing method thereof
CN106825568A (en) A kind of 3D printing manufacture method of metal matrix diamond composites and its parts
CN101451203B (en) Method for preparing SiCp/Al electronic packing part
CN105568024A (en) Preparation method for nano ceramic reinforced metal-matrix composite
CN103801695A (en) 3D printing mould-free injection forming method through metal sizing agents
CN104209498A (en) Preparing method of interface modification layer of ceramic particle enhanced metal base composite material
CN105130482B (en) A kind of Metal toughened ceramic matric composite for 3D printing
CN105648259A (en) Copper base-graphite positive gradient composite and preparation method thereof
CN113481402B (en) Preparation method of functionally gradient diamond/aluminum composite material packaging shell
CN108746555A (en) A kind of preparation method of 3D printing space structure enhancing Cu-base composites
CN105111695A (en) Conductive polymer matrix composite material with continuous conductive channel and preparation method therefor
CN106270459B (en) A kind of preparation method of copper-base pantograph slide plate
CN104384518A (en) Method for coating copper on surface of tungsten copper carbide alloy composite material
CN106222474A (en) A kind of preparation method of silver molybdenum sulfide sliding contact material
TW201313363A (en) Method for integrally forming a composite metal
CN107649684A (en) A kind of 3D printing method
CN103223525B (en) A kind of cutting Ultrathin blade
CN115138859B (en) Integrally formed diamond grinding wheel and preparation method thereof
CN106041104B (en) A kind of preparation method of lemel roughening
CN101392335A (en) Method for preparing tungsten copper composite encapsulation material
CN103924143B (en) Ti2SnC/Sn/Co electrical contact material and its production and use
CN105057659B (en) Molding method of copper base alloy powder ultrathin part
CN106346010A (en) Method for preparing additive manufacturing material
CN110627497A (en) Production method of titanium oxide niobium target material
CN103752805B (en) The manufacture method of the coated nickel of silver or iron core composite electrode wire

Legal Events

Date Code Title Description
C06 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