CN109336615B - High-toughness, wear-resistant and friction-reducing sialon-tin composite material - Google Patents

High-toughness, wear-resistant and friction-reducing sialon-tin composite material Download PDF

Info

Publication number
CN109336615B
CN109336615B CN201811463132.2A CN201811463132A CN109336615B CN 109336615 B CN109336615 B CN 109336615B CN 201811463132 A CN201811463132 A CN 201811463132A CN 109336615 B CN109336615 B CN 109336615B
Authority
CN
China
Prior art keywords
sialon
composite material
toughness
sintering
wear
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
CN201811463132.2A
Other languages
Chinese (zh)
Other versions
CN109336615A (en
Inventor
乔竹辉
孙奇春
杨军
朱圣宇
程军
于源
谈辉
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.)
Lanzhou Institute of Chemical Physics LICP of CAS
Original Assignee
Lanzhou Institute of Chemical Physics LICP 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 Lanzhou Institute of Chemical Physics LICP of CAS filed Critical Lanzhou Institute of Chemical Physics LICP of CAS
Priority to CN201811463132.2A priority Critical patent/CN109336615B/en
Publication of CN109336615A publication Critical patent/CN109336615A/en
Application granted granted Critical
Publication of CN109336615B publication Critical patent/CN109336615B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/58Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
    • C04B35/597Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon oxynitride, e.g. SIALONS
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3224Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
    • C04B2235/3225Yttrium oxide or oxide-forming salts thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3293Tin oxides, stannates or oxide forming salts thereof, e.g. indium tin oxide [ITO]
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3852Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
    • C04B2235/3865Aluminium nitrides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3852Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
    • C04B2235/3873Silicon nitrides, e.g. silicon carbonitride, silicon oxynitride
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Ceramic Products (AREA)

Abstract

The invention relates to a high-toughness wear-resistant antifriction sialon-tin composite material which is prepared by ball-milling, mixing, sintering and cooling the following components in percentage by mass to room temperature: 50.08 to 64.21wt% of Si3N47.41 to 23.39 wt% of Al2O39.40 to 16.05 wt% of AlN and 2.40 to 3.00 wt% of Y2O3And 0-24.06 wt% of SnO2Powder; wherein the sialon phase composition is Si4Al2O2N6. The sialon-tin composite material has excellent mechanical property (fracture toughness) and tribological property (low abrasion and friction coefficient) in a wide temperature range, and is particularly suitable for special workpieces which require higher toughness and keep lower frictional abrasion under the service working condition.

Description

High-toughness, wear-resistant and friction-reducing sialon-tin composite material
Technical Field
The invention relates to a composite material, in particular to a high-toughness, wear-resistant and friction-reducing sialon-tin composite material.
Background
The reliability and stability of the structural materials play a key factor in the safe, stable, and efficient operation of high-end equipment mechanical systems. The sialon ceramic has good high-temperature stability, oxidation resistance and thermal shock resistance, and has attractive application prospects in the aspects of aerospace, engine parts, metallurgy, chemical machinery and the like. However, the friction material has a disadvantage that it has a high friction coefficient and a high wear rate at high temperatures. Meanwhile, sialon ceramic materials have largely limited their wider application in structural materials due to their inherent brittleness. In addition, sialon ceramics can be generally prepared only at a relatively high temperature (the general sintering temperature is 1600 ℃), which further restricts the wide application thereof.
Therefore, the research for improving the tribological properties and mechanical properties of sialon ceramic composite materials in a wide temperature range and preparing the sialon ceramic composite materials at low temperature is increasingly paid attention, and the sialon ceramic composite materials become one of the leading subjects in the fields of material science and tribology at present.
Disclosure of Invention
The invention aims to solve the technical problem of providing a high-toughness wear-resistant antifriction sialon-tin composite material with larger melting point difference.
In order to solve the problems, the invention discloses a high-toughness, wear-resistant and friction-reducing sialon-tin composite material, which is characterized in that: the composite material is prepared by ball-milling, mixing, sintering and cooling the following components in percentage by mass to room temperature: 50.08 to 64.21wt% of Si3N4 7.41 to 23.39 wt% of Al2O39.40 to 16.05 wt% of AlN and 2.40 to 3.00 wt% of Y2O3And 0-24.06 wt% of SnO2Powder; wherein the sialon phase composition is Si4Al2O2N6
The particle size of the ball-milling mixture is 0.55-5 mu m.
The sintering condition refers to that the vacuum degree is lower than 5 x 10-1Pa, the temperature rising speed is 50-150 ℃/min, the sintering temperature is 1350-1600 ℃, the pressure is 5-20 MPa, and the heat preservation time is 5-10 min.
Compared with the prior art, the invention has the following advantages:
1. the invention starts from the angles of reducing the sintering temperature of the sialon and improving the fracture toughness and the tribology of the sialon ceramic composite material, and increases the energy dissipation of the crack in the expansion process by adding the second phase particles to improve the fracture toughness of the material. The fracture toughness of the material tested by the indentation method is found to have good fracture toughness at room temperature to 800 ℃.
2. The invention is composed of tin and sialon phase which are generated in situ and combined well, realizes the controllable preparation of the sialon ceramic (the common sintering temperature is 1600 ℃) composite material doped with tin with low melting point (the melting point is about 230 ℃) at higher sintering temperature for the first time, and provides a new strategy for preparing the composite material with larger difference of the melting points of all components.
3. The invention can effectively reduce the sintering temperature of the sialon composite material by doping tin oxide, thereby realizing the preparation of the sialon composite material at lower temperature.
4. The material prepared by the invention has excellent mechanical property, and the fracture toughness can reach 5.5 MPam1/2. Meanwhile, the material has good wear resistance and friction reduction performance, and compared with undoped sialon, the wear rate is lower by about 20 times, and the friction coefficient is as low as about 0.6.
5. The invention utilizes the uniformly distributed toughening phase (tin) to generate a friction film in the high-temperature friction process, thereby improving the contact state of a friction interface, meeting the requirements of wear resistance and wear reduction in a certain temperature range and realizing the structure/lubricating function integrated design of the ceramic composite material.
6. The invention has simple preparation process, can regulate and control the material performance by adjusting the formula and process parameters, and the prepared sialon-tin composite material has excellent mechanical property (fracture toughness) and tribological property (low abrasion and friction coefficient) in a wide temperature range, and is particularly suitable for special workpieces which require higher toughness and keep lower frictional wear under the service working condition.
Drawings
The following describes embodiments of the present invention in further detail with reference to the accompanying drawings.
FIG. 1 is a graph showing the change of the displacement of the sialon-tin composite material with temperature during the sintering process.
FIG. 2 is a graph showing the fracture toughness of the sialon-tin composite material of the present invention.
Detailed Description
Example 1A high toughness, wear resistant and friction reducing sialon-tin composite material having a sialon phase composition of Si4Al2O2N6. 64.21wt% of Si3N4、23.39wt% of Al2O39.40wt% of AlN, 3 wt% of Y2O3And (3) mixing the powder in a ball mill to obtain mixed powder with the particle size of 0.55-5 mu m. Then the mixed powder is put into a graphite die and placed in a plasma sintering furnace, and the vacuum degree is lower than 5 multiplied by 10-1And sintering under the conditions of Pa, temperature rise speed of 100 ℃/min, sintering temperature of 1600 ℃, pressure of 10MPa and heat preservation time of 10 min. And after sintering, furnace cooling to room temperature to obtain the sialon composite material named as SS 0. The shift versus sintering temperature profile during sintering is shown in fig. 1, where the sintering densification end temperature is the temperature at which the shift no longer increases. As can be seen from fig. 1, the densification end temperature of sample SS0 was 1450 ℃.
Example 2A high toughness, wear resistant and friction reducing sialon-tin composite material having a sialon phase composition of Si4Al2O2N6. 60.61 wt% of Si3N419.32 wt% of Al2O311.09 wt% of AlN, 2.85 wt% of Y2O3And 6.13 wt.% SnO2And (3) mixing the powder in a ball mill to obtain mixed powder with the particle size of 0.55-5 mu m. Then the mixed powder is put into a graphite die and is put into a plasma sintering furnace, and the vacuum degree is lower than 5 multiplied by 10-1And sintering under the conditions of Pa, temperature rise speed of 100 ℃/min, sintering temperature of 1550 ℃, pressure of 10MPa and heat preservation time of 10 min. And after sintering, furnace cooling to room temperature to obtain the sialon composite material named as SS 1.
The friction and wear test is evaluated by adopting an HT-1000 high-temperature friction and wear testing machine, and the friction coefficient and the wear rate are average values of 3 tests. The dual ball is Si3N4Ceramic, load of 5N, sliding linear velocity of 0.10m/s, friction radius of 4mm, stroke of 200m, test temperature of 25 deg.C, 400 deg.C and 800 deg.C. The results are shown in Table 1.
Table 1: example 2 sialon-based composite Material with Si3N4Friction coefficient and wear rate of ceramic ball matched pair
Figure 269706DEST_PATH_IMAGE001
As can be seen from Table 1, the friction coefficient of the obtained sialon-based composite material is 0.64-0.71 between room temperature and 800 ℃, and the wear rate is 10 at room temperature-5 mm3in/Nm, and the wear rate is an order of magnitude higher at high temperatures.
Example 3A high toughness, wear resistant and friction reducing sialon-tin composite material having a sialon phase composition of Si4Al2O2N6. 57.05wt% of Si3N415.30wt% of Al2O312.77wt% of AlN, 2.70wt% of Y2O3And 12.18 wt.% SnO2And (3) mixing the powder in a ball mill to obtain mixed powder with the particle size of 0.55-5 mu m. Then the mixed powder is put into a graphite die and placed in a plasma sintering furnace, and the vacuum degree is lower than 5 multiplied by 10-1And sintering under the conditions of Pa, temperature rise speed of 100 ℃/min, sintering temperature of 1500 ℃, pressure of 10MPa and heat preservation time of 10 min. And after sintering, furnace cooling to room temperature to obtain the sialon composite material named as SS 2.
The indentation method is then used to calculate the fracture toughness of the material, which is measured at least as an average of 9 points. The test conditions were: load 10kg, duration of loading 10s, test temperature 25 ℃, 400 ℃, and 800 ℃. The fracture toughness of the sialon-based composite material at 25-800 ℃ is shown in figure 2. As can be seen from FIG. 2, sample SS2 has good toughness between room temperature and 800 ℃ and a maximum fracture toughness of 5.5 MPam at room temperature1/2
Example 4A high toughness, wear resistant and friction reducing sialon-tin composite material having a sialon phase composition of Si4Al2O2N6. 50.08wt% of Si3N47.41 wt% of Al2O316.05 wt% of AlN, 2.40 wt% of Y2O3And 24.06 wt.% SnO2And (3) mixing the powder in a ball mill to obtain mixed powder with the particle size of 0.55-5 mu m. Then the mixed powder is filled into a graphite mould, placed in a plasma sintering furnace and subjected to vacuumDegree less than 5X 10-1Sintering under the conditions of Pa, temperature rise speed of 100 ℃/min, sintering temperature of 1450 ℃, pressure of 10MPa and heat preservation time of 10 min. And after sintering, furnace cooling to room temperature to obtain the sialon composite material named as SS 3. The variation curve of the displacement with the sintering temperature during the sintering process is shown in FIG. 1. As can be seen in FIG. 1, the densification end temperature of sample SS3 was 1345 ℃ which is a 105 ℃ reduction over that of sample SS 0. The doped tin oxide can effectively reduce the sintering temperature of the sialon composite material and realize the preparation of the sialon composite material at lower temperature.
The friction and wear test is evaluated by adopting an HT-1000 high-temperature friction and wear testing machine, and the friction coefficient and the wear rate are average values of 3 tests. The dual ball is Si3N4Ceramic, load of 5N, sliding linear velocity of 0.10m/s, friction radius of 4mm, stroke of 200m, test temperature of 25 deg.C, 400 deg.C and 800 deg.C. The results are shown in Table 2.
Table 2: sialon-based composite material of example 4 and Si3N4Friction coefficient and wear rate of ceramic ball matched pair
Figure 49444DEST_PATH_IMAGE002
As can be seen from Table 2, the obtained sialon-based composite material has excellent tribological properties at room temperature to 800 ℃, the friction coefficient is 0.6-0.71, and the wear rate is 10-5 mm3/Nm。

Claims (2)

1. A high-toughness, wear-resistant and friction-reducing sialon-tin composite material is characterized in that: the composite material is prepared by ball-milling, mixing, sintering and cooling the following components in percentage by mass to room temperature: 50.08 to 64.21wt% of Si3N4 7.41 to 23.39 wt% of Al2O39.40 to 16.05 wt% of AlN and 2.40 to 3.00 wt% of Y2O3And 6.13-24.06 wt% of SnO2Powder; wherein the sialon phase composition is Si4Al2O2N6(ii) a The particle size of the ball-milling mixture is 0.55-5 mu m.
2. A high toughness, wear resistant and friction reducing sialon-tin composite material according to claim 1 wherein: the sintering condition refers to that the vacuum degree is lower than 5 x 10-1Pa, the temperature rising speed is 50-150 ℃/min, the sintering temperature is 1350-1600 ℃, the pressure is 5-20 MPa, and the heat preservation time is 5-10 min.
CN201811463132.2A 2018-12-03 2018-12-03 High-toughness, wear-resistant and friction-reducing sialon-tin composite material Active CN109336615B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811463132.2A CN109336615B (en) 2018-12-03 2018-12-03 High-toughness, wear-resistant and friction-reducing sialon-tin composite material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811463132.2A CN109336615B (en) 2018-12-03 2018-12-03 High-toughness, wear-resistant and friction-reducing sialon-tin composite material

Publications (2)

Publication Number Publication Date
CN109336615A CN109336615A (en) 2019-02-15
CN109336615B true CN109336615B (en) 2021-06-22

Family

ID=65319987

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811463132.2A Active CN109336615B (en) 2018-12-03 2018-12-03 High-toughness, wear-resistant and friction-reducing sialon-tin composite material

Country Status (1)

Country Link
CN (1) CN109336615B (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102173716A (en) * 2011-02-24 2011-09-07 西北工业大学 Analogous ceramic high-temperature resistant friction material and preparation method thereof
CN102557647A (en) * 2011-12-13 2012-07-11 河南富耐克超硬材料股份有限公司 Polycrystalline cubic boron nitride compound material
JP5352519B2 (en) * 2010-04-08 2013-11-27 京楽産業.株式会社 Game machine
CN106795059A (en) * 2014-08-29 2017-05-31 住友电气工业株式会社 Agglomerated material, the instrument comprising agglomerated material and agglomerated material manufacture method
CN107922274A (en) * 2016-05-27 2018-04-17 住友电气工业株式会社 Agglomerated material and the cutting element for including the agglomerated material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5352519B2 (en) * 2010-04-08 2013-11-27 京楽産業.株式会社 Game machine
CN102173716A (en) * 2011-02-24 2011-09-07 西北工业大学 Analogous ceramic high-temperature resistant friction material and preparation method thereof
CN102557647A (en) * 2011-12-13 2012-07-11 河南富耐克超硬材料股份有限公司 Polycrystalline cubic boron nitride compound material
CN106795059A (en) * 2014-08-29 2017-05-31 住友电气工业株式会社 Agglomerated material, the instrument comprising agglomerated material and agglomerated material manufacture method
CN107922274A (en) * 2016-05-27 2018-04-17 住友电气工业株式会社 Agglomerated material and the cutting element for including the agglomerated material

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Ilmars Zalite等."SiAlON ceramics from nanopowders".《Journal of the European Ceramic Society》.2007,第28卷第901-905页. *
Qichun Sun等."The novel Sialon-Sn composite with high toughness and wear resistance prepared at a lower-temperature".《Tribology International》.2020,第106239-1页-第106239-9页. *

Also Published As

Publication number Publication date
CN109336615A (en) 2019-02-15

Similar Documents

Publication Publication Date Title
US20110008604A1 (en) Hard non-oxide or oxide ceramic / hard non-oxide or oxide ceramic composite hybrid article
CN107058808B (en) A kind of aluminium alloy base solid lubricating composite material and preparation method thereof
Ciudad et al. Effect of intergranular phase chemistry on the sliding-wear resistance of pressureless liquid-phase-sintered α-SiC
JP2003034581A (en) Silicon nitride abrasion resistant member and method for producing the same
JP6061592B2 (en) Friction material and friction material manufacturing method
Wei et al. Mechanical and tribological properties of hot-pressed h-BN/Si3N4 ceramic composites
JP5268750B2 (en) Impact resistant member and manufacturing method thereof
CN106011539B (en) Wide temperature range self-lubricating composite of a kind of nickel aluminium/vanadium oxide/silver and preparation method thereof
CN107584125B (en) The preparation method of grand based composites is matched in a kind of high-ductility self-lubricating
CN108774065B (en) SiC/MCMBs composite material and preparation method and application thereof
CN109336615B (en) High-toughness, wear-resistant and friction-reducing sialon-tin composite material
Kumar et al. Effects of hBN and Y2O3 Addition on Mechanical and Tribological Behavior of SiC Ceramic Matrix Composites Prepared by Spark Plasma Sintering
CN109354502B (en) Self-lubricating silicon nitride-based composite material with high wear-resistant surface in high-temperature environment
Chu et al. High‐Temperature Failure Mechanisms of Hot‐Pressed Si3N4 and Si3N4/Si3N4‐Whisker‐Reinforced Composites
CN108002844B (en) Wide-temperature-range self-lubricating sialon-based composite material
CN115925423A (en) High-performance single-phase self-lubricating high-entropy ceramic material and preparation method thereof
Santos et al. α-SiAlON–SiC composites obtained by gas-pressure sintering and hot-pressing
CN111961944B (en) Wide-temperature-range self-lubricating VN-AgMoS2Composite material and preparation method thereof
CN105198435A (en) Silicon carbide-carbon composite material and preparation method thereof
Frolova et al. Silicon carbide ceramics reinforced SiC fibers
Mazumder et al. Tribomechanical behaviour of non-oxide ceramic matrix composites in dry sliding
CN112430769A (en) Wear-resistant WC-Co-Ti3SiC2Hard alloy and preparation method thereof
CN109400174A (en) A kind of preparation method nitrogenizing silicon substrate high temperature antiwear and antifriction composite material
KR20190125524A (en) Resin material for sliding member and sliding member
CN111755085B (en) High-temperature self-compensating wear-resistant material, design method and preparation method

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