CN105418101A - Preparation method for ultrasonic-dispersed hafnium carbide silicon carbide-carbon fiber friction material - Google Patents
Preparation method for ultrasonic-dispersed hafnium carbide silicon carbide-carbon fiber friction material Download PDFInfo
- Publication number
- CN105418101A CN105418101A CN201610014268.XA CN201610014268A CN105418101A CN 105418101 A CN105418101 A CN 105418101A CN 201610014268 A CN201610014268 A CN 201610014268A CN 105418101 A CN105418101 A CN 105418101A
- Authority
- CN
- China
- Prior art keywords
- carbon fiber
- silicon carbide
- fiber blanket
- carbide
- siliconising
- 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
Links
Classifications
-
- C04B35/806—
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped 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
- C04B35/56—Shaped 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 carbides or oxycarbides
- C04B35/5607—Shaped 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 carbides or oxycarbides based on refractory metal carbides
- C04B35/5622—Shaped 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 carbides or oxycarbides based on refractory metal carbides based on zirconium or hafnium carbides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped 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
- C04B35/56—Shaped 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 carbides or oxycarbides
- C04B35/565—Shaped 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 carbides or oxycarbides based on silicon carbide
- C04B35/573—Shaped 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 carbides or oxycarbides based on silicon carbide obtained by reaction sintering or recrystallisation
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped 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
- C04B35/58—Shaped 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
- C04B35/584—Shaped 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 nitride
- C04B35/591—Shaped 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 nitride obtained by reaction sintering
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
- C04B35/65—Reaction sintering of free metal- or free silicon-containing compositions
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/42—Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
- C04B2235/428—Silicon
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/46—Gases other than oxygen used as reactant, e.g. nitrogen used to make a nitride phase
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
The invention provides a preparation method for an ultrasonic-dispersed hafnium carbide silicon carbide-carbon fiber friction material. The preparation method is characterized by comprising the steps that after carburizing treatment is performed on a graphitized carbon fiber blanket with the density of 0.1-1.8 g/cm<3>, ultrasonic-dispersed hafnium carbide filling treatment is performed, silicon carbide depositing treatment is performed, burying siliconizing treatment is performed, and then nitriding treatment is performed in a nitrogen atmosphere to prepare the ultrasonic-dispersed hafnium carbide silicon carbide-carbon fiber friction material. According to the preparation method, the graphitized carbon fiber blanket is adopted to achieve preparation of the friction material through the steps of carburizing, hafnium carbide filling, silicon carbide depositing, burying siliconizing, nitriding and the like, and the prepared friction material has the high strength, the high toughness and the high friction property and is suitable for various climate conditions.
Description
Technical field
The present invention relates to the preparation method of the friction materials of a kind of carbon fiber and stupalith compound, belong to technical field of composite preparation.
Background technology
What friction materials mainly adopted at present is carbon fiber and carbon (C/C) matrix material, and because the wear resisting property of C/C matrix material is relatively low, people are seeking the preparation method of the higher friction materials of wear resisting property.In addition, in a humid environment, its frictional behaviour can reduce C/C matrix material, brings serious potential safety hazard to use.
Summary of the invention
The object of the present invention is to provide a kind of preparation method that can overcome above-mentioned defect, realize the friction materials prepared more high strength, higher frictional behaviour and adapt to various weather condition.Its technical scheme is:
The preparation method of ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materials is 0.1 ~ 1.8g/cm by density
3graphited carbon fiber blanket carries out ultrasonic wave dispersion hafnium carbide and fills process after carrying out carburizing treatment, carry out depositing silicon carbide process again, carry out imbedding siliconising process, then in nitrogen atmosphere, nitriding treatment obtains ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materials, and concrete steps are as follows again:
(1) be 0.1 ~ 1.8g/cm by density
3graphited carbon fiber blanket passes into the mixed gas of propane flammable gas and nitrogen at 900 ~ 1100 DEG C of temperature, propane flammable gas: the mol ratio of nitrogen is 1:4 ~ 6, and flow control is at 50 ~ 600ml/min, and carburizing treatment obtains carburizing carbon fiber blanket for 10 ~ 24 hours;
(2) above-mentioned carburizing carbon fiber blanket immersion granularity being less than 0.3 μm of content is in the slurry of 5 ~ 20% hafnium carbides, be placed in ultrasonic cleaner and fill hafnium carbide process 30 ~ 50 minutes, take out dry rear obtained filling hafnium carbide carbon fiber blanket, wherein, slurry be containing ammonium polyacrylate 0.5 ~ 1.5%pH value be the aqueous solution of 9 ~ 11;
(3) above-mentioned filling hafnium carbide carbon fiber blanket is passed at 900 ~ 1100 DEG C of temperature the mixed gas of trichloromethyl silane gas, hydrogen and argon gas, depositing silicon carbide process obtains depositing silicon carbide carbon fiber blanket for 10 ~ 24 hours, wherein, trichloromethyl silane gas: hydrogen: the mol ratio of argon gas is 1:3 ~ 5:3 ~ 5, and flow is 50 ~ 600ml/min;
(4) above-mentioned depositing silicon carbide carbon fiber blanket is imbedded in siliconising material, siliconising process 3 ~ 5 hours obtained siliconising carbon fiber blankets at the temperature of 1500 ~ 1800 DEG C in vacuum atmosphere, wherein, additional 1 ~ 3% concentration of mixture of siliconising material to be silica flour 30 ~ 50% and diameter be 0.5 ~ 3mm carbon granule 50 ~ 70% is obtain after the polyvinyl alcohol water solution Homogeneous phase mixing drying of 0.2 ~ 0.6%;
(5) by above-mentioned siliconising carbon fiber blanket nitriding treatment 10 ~ 24 hours obtained ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materialss at the temperature of 1350 ~ 1700 DEG C.
Compared with prior art, its advantage is in the present invention:
1, the carbon fiber blanket that the present invention uses is graphited carbon fiber blanket, or graphited needled carbon tapetum fibrosum, or graphited weaving carbon fiber cloth, or graphited 3 D weaving carbon fiber knits block;
2, the friction materials that prepared by the present invention is by carbon fiber and silicon carbide, hafnium carbide, a kind of high strength of silicon nitride compound, high frictional behaviour, the friction materials adapted under various weather condition;
3, by carburizing, fill hafnium carbide, depositing silicon carbide, imbed the preparation that the step such as siliconising and nitrogenize realizes friction materials, carburizing and depositing silicon carbide two steps are at the carbon coating of carbon fiber surface imparting and coat of silicon carbide in order to protect carbon fiber surface not to be damaged, because coat of silicon carbide can stop the infiltration of silicon steam in the process of siliconising, coat of silicon carbide is once seepage, carbide coatings and silicon steam reaction Formed SiClx stop silicon steam further, thus protection carbon fiber surface is not damaged;
4, carbon fiber blanket has very high void content, depend merely on carburizing and depositing silicon carbide can need just can reach densification for a long time, manufacturing cost is very high, hafnium carbide is filled in employing will be very convenient with the space of the method filling carbon fiber blanket imbedding siliconising, time saving and energy saving, fill the wear resisting property that hafnium carbide can improve friction materials further simultaneously;
5, the present invention utilizes the snappiness of carburizing carbon fiber, microvesicle is produced in the slurry by hyperacoustic effect, when acoustic pressure or the sound intensity arrive to a certain degree, microvesicle will undergoes rapid expansion, then close suddenly again, the moment that microvesicle is closed produces shockwave, makes the pressure producing about 1012pa around microvesicle, hafnium carbide particle is forced to be filled in the space of carbon fiber blanket, reaches the object of calking;
6, adopt slurry dispersion hafnium carbide to fill process, effectively can improve hafnium carbide particle suspension property, improve charging efficiency, in nitridation process, generate silicon nitride hafnium carbide particle is combined securely;
7, the Pure Silicon Metal fusing point lower owing to infiltrating is about 1420 DEG C, the temperature of friction materials working face is instantaneous reaches nearly 2000 DEG C, Pure Silicon Metal nitrogenize is generated silicon nitride, form the friction materials of microvoid structure, the tolerable temperature of friction materials working face can be increased substantially, improve the performance and used life of friction materials.
Embodiment
embodiment 1
(1) be 1.8g/cm by density
3graphited carbon fiber blanket passes into the mixed gas of propane flammable gas and nitrogen at 900 DEG C of temperature, propane flammable gas: nitrogen mol ratio be 1:4, flow control is at 50ml/min, and carburizing treatment 24 hours obtains carburizing carbon fiber blanket;
(2) above-mentioned carburizing carbon fiber blanket immersion granularity being less than 0.3 μm of content is in the slurry of 5% hafnium carbide, be placed in ultrasonic cleaner and fill hafnium carbide process 50 minutes, take out dry after obtainedly fill hafnium carbide carbon fiber blanket, slurry is be the aqueous solution of 9 containing ammonium polyacrylate 1.5%pH value;
(3) above-mentioned filling hafnium carbide carbon fiber blanket is passed at 900 DEG C of temperature the mixed gas of trichloromethyl silane gas, hydrogen and argon gas, trichloromethyl silane gas: hydrogen: the mol ratio of argon gas is 1:5:5, flow control is at 50ml/min, and depositing silicon carbide process obtains depositing silicon carbide carbon fiber blanket for 24 hours;
(4) above-mentioned depositing silicon carbide carbon fiber blanket is imbedded in siliconising material, siliconising 5 hours obtained siliconising carbon fiber blankets at the temperature of 1500 DEG C in vacuum atmosphere, wherein, siliconising material is silica flour 30% and diameter, and that to be additional 5% concentration of 0.5mm carbon granule 70% be is dry obtained after the polyvinyl alcohol water solution Homogeneous phase mixing of 0.2%;
(5) by above-mentioned siliconising carbon fiber blanket nitriding treatment 10 hours obtained hafnium carbide silicon carbide―carbon fiber friction materialss at the temperature of 1700 DEG C.
embodiment 2
(1) be 0.8g/cm by density
3graphited carbon fiber blanket passes into the mixed gas of propane flammable gas and nitrogen at 1000 DEG C of temperature, propane flammable gas: nitrogen mol ratio be 1:5, flow control is at 350ml/min, and carburizing treatment 18 hours obtains carburizing carbon fiber blanket;
(2) above-mentioned carburizing carbon fiber blanket immersion granularity being less than 0.3 μm of content is in the slurry of 12% hafnium carbide, be placed in ultrasonic cleaner and fill hafnium carbide process 40 minutes, take out dry after obtainedly fill hafnium carbide carbon fiber blanket, slurry is be the aqueous solution of 10 containing ammonium polyacrylate 1%pH value;
(3) above-mentioned filling hafnium carbide carbon fiber blanket is passed at 1000 DEG C of temperature the mixed gas of trichloromethyl silane gas, hydrogen and argon gas, trichloromethyl silane gas: hydrogen: the mol ratio of argon gas is 1:4:4, flow control is at 350ml/min, and depositing silicon carbide process obtains depositing silicon carbide carbon fiber blanket for 18 hours;
(4) above-mentioned depositing silicon carbide carbon fiber blanket is imbedded in siliconising material, siliconising 4 hours obtained siliconising carbon fiber blankets at the temperature of 1650 DEG C in vacuum atmosphere, wherein, siliconising material is silica flour 40% and diameter, and that to be additional 10% concentration of 2mm carbon granule 60% be is dry obtained after the polyvinyl alcohol water solution Homogeneous phase mixing of 0.4%;
(5) by above-mentioned siliconising carbon fiber blanket nitriding treatment 18 hours obtained hafnium carbide silicon carbide―carbon fiber friction materialss at the temperature of 1550 DEG C.
embodiment 3
(1) be 0.1g/cm by density
3graphited carbon fiber blanket passes into the mixed gas of propane flammable gas and nitrogen at 1100 DEG C of temperature, propane flammable gas: nitrogen mol ratio be 1:6, flow control is at 600ml/min, and carburizing treatment 10 hours obtains carburizing carbon fiber blanket;
(2) above-mentioned carburizing carbon fiber blanket immersion granularity being less than 0.3 μm of content is in the slurry of 20% hafnium carbide, be placed in ultrasonic cleaner and fill hafnium carbide process 30 minutes, take out dry after obtainedly fill hafnium carbide carbon fiber blanket, slurry is be the aqueous solution of 11 containing ammonium polyacrylate 0.5%pH value;
(3) above-mentioned filling hafnium carbide carbon fiber blanket is passed at 1100 DEG C of temperature the mixed gas of trichloromethyl silane gas, hydrogen and argon gas, trichloromethyl silane gas: hydrogen: the mol ratio of argon gas is 1:3:3, flow control is at 600ml/min, and depositing silicon carbide process obtains depositing silicon carbide carbon fiber blanket for 10 hours;
(4) above-mentioned depositing silicon carbide carbon fiber blanket is imbedded in siliconising material, siliconising 3 hours obtained siliconising carbon fiber blankets at the temperature of 1800 DEG C in vacuum atmosphere, wherein, siliconising material is silica flour 50% and diameter, and that to be additional 15% concentration of 3mm carbon granule 50% be is dry obtained after the polyvinyl alcohol water solution Homogeneous phase mixing of 0.6%;
(5) by above-mentioned siliconising carbon fiber blanket nitriding treatment 24 hours obtained hafnium carbide silicon carbide―carbon fiber friction materialss at the temperature of 1350 DEG C.
Claims (1)
1. the preparation method of ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materials, it is characterized in that, be 0.1 ~ 1.8g/cm by density
3graphited carbon fiber blanket carries out ultrasonic wave dispersion hafnium carbide and fills process after carrying out carburizing treatment, carry out depositing silicon carbide process again, carry out imbedding siliconising process, then in nitrogen atmosphere, nitriding treatment obtains ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materials, and concrete steps are as follows again:
(1) be 0.1 ~ 1.8g/cm by density
3graphited carbon fiber blanket passes into the mixed gas of propane flammable gas and nitrogen at 900 ~ 1100 DEG C of temperature, propane flammable gas: the mol ratio of nitrogen is 1:4 ~ 6, and flow control is at 50 ~ 600ml/min, and carburizing treatment obtains carburizing carbon fiber blanket for 10 ~ 24 hours;
(2) above-mentioned carburizing carbon fiber blanket immersion granularity being less than 0.3 μm of content is in the slurry of 5 ~ 20% hafnium carbides, be placed in ultrasonic cleaner and fill hafnium carbide process 30 ~ 50 minutes, take out dry rear obtained filling hafnium carbide carbon fiber blanket, wherein, slurry be containing ammonium polyacrylate 0.5 ~ 1.5%pH value be the aqueous solution of 9 ~ 11;
(3) above-mentioned filling hafnium carbide carbon fiber blanket is passed at 900 ~ 1100 DEG C of temperature the mixed gas of trichloromethyl silane gas, hydrogen and argon gas, depositing silicon carbide process obtains depositing silicon carbide carbon fiber blanket for 10 ~ 24 hours, wherein, trichloromethyl silane gas: hydrogen: the mol ratio of argon gas is 1:3 ~ 5:3 ~ 5, and flow is 50 ~ 600ml/min;
(4) above-mentioned depositing silicon carbide carbon fiber blanket is imbedded in siliconising material, siliconising process 3 ~ 5 hours obtained siliconising carbon fiber blankets at the temperature of 1500 ~ 1800 DEG C in vacuum atmosphere, wherein, additional 1 ~ 3% concentration of mixture of siliconising material to be silica flour 30 ~ 50% and diameter be 0.5 ~ 3mm carbon granule 50 ~ 70% is obtain after the polyvinyl alcohol water solution Homogeneous phase mixing drying of 0.2 ~ 0.6%;
(5) by above-mentioned siliconising carbon fiber blanket nitriding treatment 10 ~ 24 hours obtained ultrasonic wave dispersion hafnium carbide silicon carbide―carbon fiber friction materialss at the temperature of 1350 ~ 1700 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610014268.XA CN105418101B (en) | 2016-01-11 | 2016-01-11 | Ultrasonic wave disperses the preparation method of hafnium carbide carborundum carbon fiber friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610014268.XA CN105418101B (en) | 2016-01-11 | 2016-01-11 | Ultrasonic wave disperses the preparation method of hafnium carbide carborundum carbon fiber friction material |
Publications (2)
Publication Number | Publication Date |
---|---|
CN105418101A true CN105418101A (en) | 2016-03-23 |
CN105418101B CN105418101B (en) | 2018-01-30 |
Family
ID=55496720
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610014268.XA Expired - Fee Related CN105418101B (en) | 2016-01-11 | 2016-01-11 | Ultrasonic wave disperses the preparation method of hafnium carbide carborundum carbon fiber friction material |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105418101B (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101830703A (en) * | 2010-04-06 | 2010-09-15 | 中南大学 | Carbon fiber reinforced boron carbide composite material and preparation method thereof |
CN102617178A (en) * | 2012-04-16 | 2012-08-01 | 中国人民解放军国防科学技术大学 | C/SiC composite material, preparation method of composite material and friction plate |
CN103342570A (en) * | 2013-07-11 | 2013-10-09 | 山东宝纳新材料有限公司 | Method for preparing C/SiC composite material through low-cost fused silicon impregnation method |
CN104150958A (en) * | 2014-08-08 | 2014-11-19 | 苏州宏久航空防热材料科技有限公司 | Repair method for ceramic matrix composite material |
-
2016
- 2016-01-11 CN CN201610014268.XA patent/CN105418101B/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101830703A (en) * | 2010-04-06 | 2010-09-15 | 中南大学 | Carbon fiber reinforced boron carbide composite material and preparation method thereof |
CN102617178A (en) * | 2012-04-16 | 2012-08-01 | 中国人民解放军国防科学技术大学 | C/SiC composite material, preparation method of composite material and friction plate |
CN103342570A (en) * | 2013-07-11 | 2013-10-09 | 山东宝纳新材料有限公司 | Method for preparing C/SiC composite material through low-cost fused silicon impregnation method |
CN104150958A (en) * | 2014-08-08 | 2014-11-19 | 苏州宏久航空防热材料科技有限公司 | Repair method for ceramic matrix composite material |
Also Published As
Publication number | Publication date |
---|---|
CN105418101B (en) | 2018-01-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105439602A (en) | Preparation method of resin dispersed titanium carbide silicon carbide-carbon fiber friction material | |
CN105418102A (en) | Preparation method for ultrasonically dispersed hafnium boride-silicon carbide-carbon fiber friction material | |
CN105418128A (en) | Preparation method for ultrasonic-dispersed vanadium carbide boron carbide-carbon fiber friction material | |
CN105418127A (en) | Preparation method for ultrasonically dispersed hafnium boride-boron carbide-carbon fiber friction material | |
CN105418126A (en) | Preparation method for ultrasonically dispersed niobium boride-boron carbide-carbon fiber friction material | |
CN105439593A (en) | Preparation method for ethanol dispersed zirconium carbide boron carbide-carbon fiber friction material | |
CN105481426A (en) | Preparing method for ethanol-dispersed vanadium carbide boron carbide and carbon fiber friction material | |
CN105481433A (en) | Method for preparing ethyl alcohol dispersion zirconium boride silicon carbide-carbon fiber friction material | |
CN105418113A (en) | Preparing method for ethanol-dispersed hafnium boride silicon carbide and carbon fiber friction material | |
CN105481436A (en) | Method for preparing ethyl alcohol dispersion tantalum boride silicon carbide-carbon fiber friction material | |
CN105439595A (en) | Preparation method for ethanol dispersed tungsten carbide boron carbide-carbon fiber friction material | |
CN105439597A (en) | Preparation method for ethanol dispersed titanium boride silicon carbide-carbon fiber friction material | |
CN105418101A (en) | Preparation method for ultrasonic-dispersed hafnium carbide silicon carbide-carbon fiber friction material | |
CN105418099A (en) | Preparation method for ultrasonic-dispersed titanium carbide silicon carbide-carbon fiber friction material | |
CN105481419A (en) | Preparation method of ultrasonic dispersion zirconium carbide silicon carbide-carbon fiber friction material | |
CN105439589A (en) | Preparation method of ultrasonic-dispersion niobium and carbide silicon carbide-carbon fiber friction material | |
CN105481415A (en) | Method for preparing ultrasonic dispersion tantalum boride silicon carbide-carbon fiber friction material | |
CN105481452A (en) | Preparation method of ultrasonic dispersion hafnium carbide and boron carbide-carbon fiber friction material | |
CN105481456A (en) | Preparation method of ultrasonic dispersion tantalum carbide and boron carbide-carbon fiber friction material | |
CN105481418A (en) | Method for preparing ultrasonic dispersion zirconium diboride silicon carbide-carbon fiber friction material | |
CN105439590A (en) | Preparation method of ultrasonic-dispersion tungsten carbide and silicon carbide-carbon fiber friction material | |
CN105418100A (en) | Preparation method for ultrasonically dispersed vanadium boride-silicon carbide-carbon fiber friction material | |
CN105481417A (en) | Preparation method of ultrasonic dispersion titanium boride silicon carbide-carbon fiber friction material | |
CN105481416A (en) | Preparation method of ultrasonic dispersion niobium boride silicon carbide-carbon fiber friction material | |
CN105481457A (en) | Preparation method of ultrasonic dispersion tungsten carbide and boron carbide-carbon fiber friction 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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20180130 Termination date: 20220111 |