CN104561882A - High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating - Google Patents
High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating Download PDFInfo
- Publication number
- CN104561882A CN104561882A CN201510049985.1A CN201510049985A CN104561882A CN 104561882 A CN104561882 A CN 104561882A CN 201510049985 A CN201510049985 A CN 201510049985A CN 104561882 A CN104561882 A CN 104561882A
- Authority
- CN
- China
- Prior art keywords
- coating
- temperature oxidation
- oxidation resistant
- powder
- resistant coating
- 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
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Coating By Spraying Or Casting (AREA)
Abstract
The invention belongs to the field of thermal spraying, and relates to a high-temperature oxidation resistant coating on a niobium alloy surface and a preparation method of the high-temperature oxidation resistant coating. The coating is in a dual-layer structure with a bottom coating Mo1-xWx(Si1-y-zAlyBz)2 and a surface coating Mo1-xWx(Si1-y-zAlyBz)2-(10-20)%wt HfSi2, and prepared on a niobium alloy matrix surface by a high-energy plasma spraying process, wherein a bottom coating powder material Mo1-xWx(Si1-y-zAlyBz)2 is prepared by a self-propagating process, and the spherical particles meeting the requirements of the spraying process are obtained by applying a plasma spheroidizing process; surface coating powder materials Mo1-xWx(Si1-y-zAlyBz)2 and HfSi2 are mixed evenly in a mechanical mixing manner. The coating has excellent high-temperature oxidation resistance at 1500-1800 DEG C, and can be applied to high-temperature protection of niobium alloy parts.
Description
Technical field
The invention belongs to field of thermal spray, relate to a kind of High Temperature Oxidation Resistant Coating on Nb, the high-temperature oxidation resistant being particularly applicable to the key part niobium alloy substrate surfaces such as rocket engine, guided missile, nuclear reactor aircraft wings and rudder protects.
Background technology
Niobium alloy has the advantages such as excellent mechanical behavior under high temperature, high-melting-point, solid solution ability be strong, can be used for preparing the key parts such as rocket engine, guided missile, nuclear reactor, aircraft wings and rudder.But the antioxidant property of niobium alloy is poor, namely there is oxidative phenomena at 600 DEG C in pure metal niobium, had a strong impact on its application under high temperature aerobic environment.Therefore, the high-temperature oxidation resistance of niobium alloy must be improved, to expand its application space.The main path improving niobium alloy oxidation-resistance property has alloying and top coat protection.Alloying refers to adds the elements such as Si, Cr, Al, Ti, V in niobium and alloy thereof, makes its Surface Creation oxide film when high temperature is applied, thus improves its oxidation-resistance.Though adding of alloy can improve antioxidant property, also can cause the decline of material at high temperature mechanical property simultaneously, have the limitation of himself.Top coat not only can protect matrix not by high temperature corrosion, also can the mechanical behavior under high temperature of farthest reserved materials, is to take into account mechanical behavior under high temperature and the effective approach of antioxidant property.
Niobium alloy high temperature coatings system is divided into refractory alloy coating, noble coatings, aluminide coating and silicide coating.Silicide coating is the coating be most widely used at present, comprises Nb (Ti)-Si coating system, Si-Cr-Ti (Fe) coating system and Mo-Si coating system.Nb (Ti)-Si coating system can be used for the oxidation protection of less than 1300 DEG C niobium alloy component surfaces.The exploitation of Si-Cr-Ti (Fe) coating system comparatively early, be successfully applied to the airship of multiple model and the surfacecti proteon of rocket engine niobium alloy component, but its use temperature is also no more than 1400 DEG C.Along with the application of novel double elements track attitude control engine, niobium alloy parts need life-time service under hyperthermal environments, intermetallic compound MoSi
2coating at high temperature can be oxidized and generate volatile MoO
3with the SiO with self-healing capability
2protective membrane, effectively stoping oxygen to the diffusion of base material direction, is the most promising coated material in silicide coating.But MoSi
2very crisp under room temperature, under low temperature, (300 ~ 700 DEG C) have oxidative phenomena, and high temperature (more than 1250 DEG C) intensity is low.The niobium alloy high temperature coatings obtained in above-mentioned prior art is single-layer coating, and cannot be used for temperature higher than the aerobic environment of 1400 DEG C, therefore needs MoSi
2carry out modification to meet its service requirements under high temperature aerobic environment.
Summary of the invention
The object of this invention is to provide a kind of High Temperature Oxidation Resistant Coating on Nb, Mo-Si system coating is improved, oxidation-resistance and the high-temperature stability of coating can be improved, to meet its service requirements under high temperature aerobic environment.
Another object of the present invention is the preparation method obtaining above-mentioned High Temperature Oxidation Resistant Coating on Nb, and adopt high energy plasma spraying coating process at niobium alloy surface direct operation, technique is simple, convenient operation and realization.
To achieve these goals, the invention provides following technical scheme:
A kind of High Temperature Oxidation Resistant Coating on Nb niobium alloy matrix 1 is undercoat 2 and the finishing coat 3 of following composition: undercoat 2 is Mo
1-xw
x(Si
1-y-zal
yb
z)
2, finishing coat 3 is HfSi
210-20wt%, all the other are Mo
1-xw
x(Si
1-y-zal
yb
z)
2; In formula, x, y and z represent the mole number of corresponding element respectively, and 0 < x≤0.5,0.1≤y < 0.5,0 < z≤0.4,0.1 < y+z≤0.5.
In formula, the mole number of x, y and z can be: 0.1≤x≤0.5,0.1≤y≤0.4,0.1≤z≤0.4,0.2≤y+z≤0.5.
The total thickness of this coating is 0.2 ~ 0.3mm, and undercoat accounts for 40 ~ 60% of total thickness.
This coating is under hot operation state, and B element can form borosilicate protective layer, the HfSi in finishing coat
2hfO can be generated under high temperature oxidation
2with the SiO with self-healing capability
2.
Undercoat 2 wherein and finishing coat 3 adopt high energy plasma spraying coating process to prepare, Mo wherein
1-xw
x(Si
1-y-zal
yb
z)
2dusty spray material adopts the preparation of self-propagating technique.
A preparation method for High Temperature Oxidation Resistant Coating on Nb, the method adopts high energy plasma spraying coating process, comprises the steps:
(1) raw material Mo, W, Si, Al and B powder is pressed chemical formula Mo
1-xw
x(Si
1-y-zal
yb
z)
2in molar ratio ingredient, wherein 0 < x≤0.5,0.1≤y < 0.5,0 < z≤0.4,0.1 < y+z≤0.5; Then use high energy ball mill ball milling, powdered material is mixed;
(2) above-mentioned mixing powdered material oven drying at low temperature pressed compact is shaped;
(3) shaping block material is put into self-propagating reaction stove to carry out Self-propagating Sintering Synthetic and be obtained by reacting Mo
1-xw
x(Si
1-y-zal
yb
z)
2product;
(4) with jaw crusher by the material fragmentation powdered after abundant self-propagating reaction;
(5) sieve the mixed powder choosing granularity 40 ~ 80 μm and carry out induction plasma spheroidizing, obtain spherical powder particle, sieve the powder got within the scope of particle diameter 40 ~ 80 μm, obtain high-temperature oxidation resistant coating primer;
(6) by the HfSi of the powder after plasma spheroidization and 10% ~ 20wt%
2powder adopts the mode of mechanically mixing to mix, and obtains high-temperature oxidation resistant coating surface material;
(7) purifying treatment and sandblasting roughening treatment are carried out in spraying body material niobium alloy surface;
(8) high energy plasma spraying coating process is adopted to prepare bottom and surface layer on niobium alloy surface.
Described step (1) Raw powder is purity>=99.9%, and the powder that granularity is 1 ~ 3 μm puts into alcohol and ZrO in Process During High Energy Ball Milling
2abrading-ball, ball material mass ratio is 3:1, high energy ball mill Ball-milling Time 14 ~ 18 hours.
The compacted density > 40% of described step (2).
In described step (3), the two sections of electric wires connecting ignition switch are placed in one end of compressing powder, connect with tungsten filament between electric wire, with Ti-Si powder for detonator, mass ratio is Ti:Si=3:1; Before reaction, vacuum tightness-0.1MPa in self-propagating stove, is filled with argon shield, to Ar Pressure force value 0.6MPa, then presses ignition switch, light tungsten filament, starts reaction.
In described step (7), sandblasting roughening treatment is to niobium alloy surfaceness 6 ~ 12 μm.
Compared with niobium alloy surface oxidation-resistant coating of the prior art, beneficial effect of the present invention is:
1) inside Mo-Si system coating, add W, the elements such as Al, B, improve the intensity under coating high-temp and toughness, improve oxidation-resistance and the high-temperature stability of coating.
2) adopt bilayer structure, reduce not mating of heat physical properties between coating with body material, refinement coating structure, is conducive to the thermal cycle life improving coating.
3) adopt Self-propagating Sintering Synthetic reaction to prepare composite powder, and apply the spherical powder that induction plasma spheriodizing technique obtains adapting to spraying coating process demand, application high energy plasma spraying coating process prepares coating, and technique is simple, convenient operation and realization.
Accompanying drawing illustrates:
Fig. 1 is coating structure schematic diagram
Reference numeral is wherein: 1 niobium alloy, 2 undercoats, 3 finishing coats
Embodiment
Below in conjunction with embodiment, the present invention is further described.
Key problem in technology of the present invention is, 1) composition of Mo-Si system coating is improved, and add the elements such as W, Al, B; 2) structure of this coating and preparation method are improved.
In composition improvement
Coating of the present invention comprises double-layer structure: bottom is Mo
1-xw
x(Si
1-y-zal
yb
z)
2coating, surface layer is Mo
1-xw
x(Si
1-y-zal
yb
z)
2-(10-20) %wtHfSi
2coating, (wherein 0 < x≤0.5,0.1≤y < 0.5,0 < z≤0.4,0.1 < y+z≤0.5).
Add W in primer coat material and can improve MoSi
2the intensity of coating, strengthens coating stability at high temperature; Add Al and can improve MoSi
2the toughness of coating and high-temperature oxidation resistance, adding B can at high temperature form borosilicate protective layer, improves the antioxidant property of coating.HfSi is added in surface layer
2coating can be made under high temperature oxidation to generate HfO
2with the SiO with self-healing capability
2, HfO
2can refinement coating structure, improve toughness.Described coating all adopts high energy plasma spraying coating process directly to prepare on niobium alloy surface.
In the preparation of coating
High Temperature Oxidation Resistant Coating on Nb of the present invention, prepares the Mo of bottom respectively
1-xw
x(Si
1-y-zal
yb
z)
2coating, and the Mo of surface layer
1-xw
x(Si
1-y-zal
yb
z)
2-(10-20) %wtHfSi
2coating, wherein:
1) bottom Mo
1-xw
x(Si
1-y-zal
yb
z)
2coating, adopts the preparation of high energy plasma spraying coating process.Required Mo
1-xw
x(Si
1-y-zal
yb
z)
2dusty spray material adopts the preparation of self-propagating technique.Self-propagating technique prepares Mo
1-xw
x(Si
1-y-zal
yb
z)
2coated powder MATERIALS METHODS is as follows: by Mo powder (Mo content 99.99%, powder size 1 ~ 3 μm), W powder (W content 99.99%, powder size 1 ~ 3 μm), Si powder (Si content 99.99%, powder size 1 ~ 3 μm), Al powder (Al content 99.9%, powder size 1 ~ 3 μm), B powder (B content 99.9%, powder size 1 ~ 3 μm) is by Mo
1-xw
x(Si
1-y-zal
yb
z)
2molar ratio (wherein 0 < x≤0.5 of each element in chemical formula, 0.1≤y < 0.5, 0 < z≤0.4, 0.1 < y+z≤0.5), the block of density > 40% is pressed into after adopting high-energy ball milling fully to mix, then be placed in self-propagating reaction device and carry out self-propagating reaction, after question response fully completes, material fragmentation is become the powder of granularity 40 ~ 80 μm, finally spheroidizing of powder is the spherical or subsphaeroidal particle of good fluidity by employing induction plasma spheriodizing technique, sieve gets the powder of particle diameter within the scope of 40 ~ 80 μm, to adapt to the demand of spraying coating process.
The principle of induction plasma spheriodizing technique: powder sends into the high-temperature area of plasma body under the effect of carrier gas, be heated to molten state, melted powder enters in reaction chamber, the drop that sphericity is very high is formed under capillary effect, quick solidification within the extremely short time, thus obtain spherical powder particle.Processing parameter is as shown in table 1.
Table 1 induction plasma spheriodizing technique parameter
High energy plasma spray-on coating processing parameter is as shown in table 2:
Table 2 high energy plasma spraying parameter
2) surface layer is Mo
1-xw
x(Si
1-y-zal
yb
z)
2-(10 ~ 20) %wtHfSi
2coating, adopts the preparation of high energy plasma spraying coating process.Wherein, required Mo
1-xw
x(Si
1-y-zal
yb
z)
2dusty spray material adopts the preparation of self-propagating technique, powder diameter 40 ~ 80 μm; HfSi
2powder diameter 40 ~ 80 μm; Two kinds of powder are prepared in mass ratio rear employing mechanically mixing mode and make it uniform composition, then spray.
3) at bottom Mo
1-xw
x(Si
1-y-zal
yb
z)
2+ surface layer Mo
1-xw
x(Si
1-y-zal
yb
z)
2-(10 ~ 20) %wtHfSi
2in bilayer structure, total coating thickness is 0.2 ~ 0.3mm, and bottom and surface layer thickness separately can require to adjust according to the applying working condition of niobium alloy.
Embodiment
The present invention gives embodiment 1-5, the chemical constitution of each embodiment is as shown in table 3, adopts following technique to prepare:
1, powder preparation
Mo
1-xw
x(Si
1-y-zal
yb
z)
2the chemical constitution of powdered material is as shown in table 3.
Table 3 Mo
1-xw
x(Si
1-y-zal
yb
z)
2the chemical constitution of powdered material and corresponding molar percentage
By Mo powder, W powder, Si powder, Al powder, B powder is configured respectively by the molar content shown in table 1, puts into suitable alcohols and ZrO
2abrading-ball, ball material mass ratio is 3:1, puts into ball grinder, adopts high energy ball mill ball milling 16 hours, powder is fully mixed.After abrading-ball takes out, powdered material oven drying at low temperature pressed compact is shaped, guarantees compacted density > 40%, be then placed in self-propagating reaction device and carry out self-propagating reaction.Self-propagating reaction lights reactant base substrate by external heat source (high temperature pulse of moment) local, combustion wave is propagated with the form spread subsequently, and material is released a large amount of reaction heat and made reaction continue to carry out thus generate the method for powder in building-up process.Concrete steps are as follows: the one end two sections of electric wires connecting ignition switch being placed in compressing powder, connects with tungsten filament between electric wire, with Ti-Si powder for detonator, and mass ratio 3:1.Before reaction, in self-propagating stove, vacuum tightness-0.1MPa, is filled with argon shield, to Ar Pressure force value 0.6MPa.Press ignition switch, light tungsten filament, as Ar Pressure in stove raises, illustrate that reactant successfully ignites, start reaction.Reaction ignition reaction thing base substrate, combustion wave is propagated with the form spread subsequently, and a large amount of reaction heat released by material in building-up process makes reaction continue to carry out, until generate powder.
Reaction equation is as follows:
(1-x)Mo+xW+2(1-y-z)Si+2yAl+2zB=Mo
1-xW
x(Si
1-y-zAl
yB
z)
2
After question response fully completes, by material fragmentation, the mixed powder of granularity 40 ~ 80 μm is chosen in screening, and spheroidizing of powder is the spherical or subsphaeroidal particle of good fluidity by application induction plasma spheriodizing technique, sieve the powder got within the scope of particle diameter 40 ~ 80 μm, packed for standby use.
By the powder of the above-mentioned 5 kinds of chemical constitutions after plasma spheroidization respectively and HfSi
2powder mixes according to mass ratio 9:1, adopts the mode of mechanically mixing to mix powder, time 2 h, by stand-by for mixed powder packaging.
2, coating preparation
Niobium 521 alloy selected by spraying body material.Before spraying, purifying treatment is carried out in niobium alloy surface first, removes surface smut with acetone.And sandblasting roughening treatment is carried out in rear surface, sandblasting can meet spraying requirement to surfaceness 6 ~ 12 μm.Adopt high energy plasma spraying coating process at niobium alloy surface preparation Mo afterwards
1-xw
x(Si
1-y-zal
yb
z)
2bottom+Mo
1-xw
x(Si
1-y-zal
yb
z)
2-HfSi
2surface layer, bottom and surface layer coat-thickness are 0.1mm.For guaranteeing that coating sample does not peel off because of the oxidation of body material in early days in oxidation test process, all exposed surfaces of niobium alloy matrix all need the coating spraying said structure.
3, coating antioxidant property and cold-hot impact property
Test above-mentioned five kinds of coatings in the static state anti-oxidant life-span of 1500 ~ 1800 DEG C and the cold-and-heat resistent impact property of 1700 DEG C ~ 1800 DEG C.
Static anti-oxidant life test: be coated with and be placed in process furnace, is incubated at assigned temperature under guarantee stove internal oxidition atmospheric condition, until disbonding lost efficacy, and off-test.
Cold-and-heat resistent impact property is tested: wash away 10min in the oxydizing flame atmosphere of coating under assigned temperature, be cooled to room temperature, be called a cold cycling.Circulation like this is repeatedly until defective coatings off-test.
Coating antioxidant property and thermal shock performance as shown in table 4.
Table 4 coating antioxidant property and thermal shock performance
Claims (10)
1. a High Temperature Oxidation Resistant Coating on Nb, is characterized in that: the upper undercoat (2) for following composition of niobium alloy matrix (1) and finishing coat (3): undercoat (2) is Mo
1-xw
x(Si
1-y-zal
yb
z)
2, finishing coat (3) is HfSi
210-20wt%, all the other are Mo
1-xw
x(Si
1-y-zal
yb
z)
2; In formula, x, y and z represent the mole number of corresponding element respectively, and 0 < x≤0.5,0.1≤y < 0.5,0 < z≤0.4,0.1 < y+z≤0.5.
2. High Temperature Oxidation Resistant Coating on Nb as claimed in claim 1, is characterized in that: 0.1≤x≤0.5,0.1≤y≤0.4,0.1≤z≤0.4,0.2≤y+z≤0.5.
3. High Temperature Oxidation Resistant Coating on Nb as claimed in claim 1, is characterized in that: the total thickness of this coating is 0.2 ~ 0.3mm, and undercoat accounts for 40 ~ 60% of total thickness.
4. High Temperature Oxidation Resistant Coating on Nb as claimed in claim 1, is characterized in that: this coating is under hot operation state, and B element can form borosilicate protective layer, the HfSi in finishing coat
2hfO can be generated under high temperature oxidation
2with the SiO with self-healing capability
2.
5. High Temperature Oxidation Resistant Coating on Nb as claimed in claim 1, is characterized in that: undercoat (2) wherein and finishing coat (3) adopt the preparation of high energy plasma spraying coating process, Mo wherein
1-xw
x(Si
1-y-zal
yb
z)
2dusty spray material adopts the preparation of self-propagating technique.
6. a preparation method for High Temperature Oxidation Resistant Coating on Nb according to claim 1, is characterized in that: the method adopts high energy plasma spraying coating process, comprises the steps:
(1) raw material Mo, W, Si, Al and B powder is pressed chemical formula Mo
1-xw
x(Si
1-y-zal
yb
z)
2in molar ratio ingredient, wherein 0 < x≤0.5,0.1≤y < 0.5,0 < z≤0.4,0.1 < y+z≤0.5; Then use high energy ball mill ball milling, powdered material is mixed;
(2) above-mentioned mixing powdered material oven drying at low temperature pressed compact is shaped;
(3) shaping block material is put into self-propagating reaction stove to carry out Self-propagating Sintering Synthetic and be obtained by reacting Mo
1-xw
x(Si
1-y-zal
yb
z)
2product;
(4) with jaw crusher by the material fragmentation powdered after abundant self-propagating reaction;
(5) sieve the mixed powder choosing granularity 40 ~ 80 μm and carry out induction plasma spheroidizing, obtain spherical powder particle, sieve the powder got within the scope of particle diameter 40 ~ 80 μm, obtain high-temperature oxidation resistant coating primer;
(6) by the HfSi of the powder after plasma spheroidization and 10% ~ 20wt%
2powder adopts the mode of mechanically mixing to mix, and obtains high-temperature oxidation resistant coating surface material;
(7) purifying treatment and sandblasting roughening treatment are carried out in spraying body material niobium alloy surface;
(8) high energy plasma spraying coating process is adopted to prepare bottom and surface layer on niobium alloy surface.
7. the preparation method of a kind of High Temperature Oxidation Resistant Coating on Nb as claimed in claim 6, it is characterized in that: described step (1) Raw powder is purity>=99.9%, the powder that granularity is 1 ~ 3 μm, puts into alcohol and ZrO in Process During High Energy Ball Milling
2abrading-ball, ball material mass ratio is 3:1, high energy ball mill Ball-milling Time 14 ~ 18 hours.
8. the preparation method of a kind of High Temperature Oxidation Resistant Coating on Nb as claimed in claim 6, is characterized in that: the compacted density > 40% of described step (2).
9. the preparation method of a kind of High Temperature Oxidation Resistant Coating on Nb as claimed in claim 6, it is characterized in that: in described step (3), the two sections of electric wires connecting ignition switch are placed in one end of compressing powder, connect with tungsten filament between electric wire, with Ti-Si powder for detonator, mass ratio is Ti:Si=3:1; Before reaction, vacuum tightness-0.1MPa in self-propagating stove, is filled with argon shield, to Ar Pressure force value 0.6MPa, then presses ignition switch, light tungsten filament, starts reaction.
10. the preparation method of a kind of High Temperature Oxidation Resistant Coating on Nb as claimed in claim 6, is characterized in that: in described step (7), sandblasting roughening treatment is to niobium alloy surfaceness 6 ~ 12 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510049985.1A CN104561882B (en) | 2015-01-30 | 2015-01-30 | High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510049985.1A CN104561882B (en) | 2015-01-30 | 2015-01-30 | High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating |
Publications (2)
Publication Number | Publication Date |
---|---|
CN104561882A true CN104561882A (en) | 2015-04-29 |
CN104561882B CN104561882B (en) | 2017-01-11 |
Family
ID=53078943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510049985.1A Expired - Fee Related CN104561882B (en) | 2015-01-30 | 2015-01-30 | High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104561882B (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104928613A (en) * | 2015-06-05 | 2015-09-23 | 柳州弘天科技有限公司 | Preparation method for machining cutter |
CN104947031A (en) * | 2015-06-05 | 2015-09-30 | 柳州弘天科技有限公司 | Manufacturing method of mechanical machining tool |
CN105112915A (en) * | 2015-04-30 | 2015-12-02 | 宁夏东方钽业股份有限公司 | Oxidation-resistant material and method employing same for preparing tantalum-tungsten alloy anti-oxidation coating |
CN105458269A (en) * | 2015-12-01 | 2016-04-06 | 南通大学 | Manufacturing method of wear-proof coating |
CN106048488A (en) * | 2016-06-21 | 2016-10-26 | 西安理工大学 | Method of preparing high-temperature oxidation-resistant coating on surface of refractory metal material |
CN105290389B (en) * | 2015-11-13 | 2018-02-06 | 航天材料及工艺研究所 | A kind of micro-satellite cluster thrust chamber slurry and its preparation method and application |
CN107841705A (en) * | 2017-11-09 | 2018-03-27 | 段占娥 | A kind of method for preparing anti-oxidant refractory metal coating |
CN113308689A (en) * | 2021-05-14 | 2021-08-27 | 宁夏东方钽业股份有限公司 | Novel niobium-tungsten alloy high-temperature oxidation-resistant coating material and preparation method thereof |
CN113913723A (en) * | 2021-12-14 | 2022-01-11 | 矿冶科技集团有限公司 | Micron-sized porous-structure thermal barrier coating powder and preparation method thereof |
CN114182251A (en) * | 2021-11-09 | 2022-03-15 | 北京神箭空天科技有限公司 | High-temperature protective coating for jet pipe of aerospace vehicle engine and preparation method and application thereof |
CN114672805A (en) * | 2022-04-29 | 2022-06-28 | 中北大学 | Preparation method of high-temperature oxidation resistant coating on surface of niobium alloy |
CN116253569A (en) * | 2023-01-04 | 2023-06-13 | 河南省科学院碳基复合材料研究院 | Preparation of (Hf, ta) B by using self-propagating auxiliary solid solution doping technology 2 -MoSi 2 Method for preparing oxygen-resistant coating |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6240364A (en) * | 1985-08-15 | 1987-02-21 | Nec Corp | Formation of high melting point metal silicide |
JPS6272122A (en) * | 1985-09-25 | 1987-04-02 | Nec Corp | High melting point metal silicide formation |
US20060228475A1 (en) * | 2003-05-01 | 2006-10-12 | Wisconsin Alumni Research Foundation | Oxidation resistant coatings for ultra high temperature transition metals and transition metal alloys |
CN1948218A (en) * | 2006-10-19 | 2007-04-18 | 宁夏东方钽业股份有限公司 | High temperature anti oxidation material and high temperature antioxidation coating layer prepared from same |
CN101200801A (en) * | 2007-12-18 | 2008-06-18 | 中南大学 | Niobic alloy high temperature antioxidation silicide coating and preparation method thereof |
CN101200372A (en) * | 2006-10-19 | 2008-06-18 | 宁夏东方钽业股份有限公司 | High-temperature oxidation-resistant material and high-temperature anti-oxidation coating prepared thereby |
CN102851635A (en) * | 2012-09-20 | 2013-01-02 | 河北联合大学 | Mo-C-N-Si-Nb gradient coating material and preparation method thereof |
CN104120426A (en) * | 2014-07-25 | 2014-10-29 | 北京航空航天大学 | Mo-Si-B coating on niobium-based alloy and preparation method of Mo-Si-B coating |
-
2015
- 2015-01-30 CN CN201510049985.1A patent/CN104561882B/en not_active Expired - Fee Related
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6240364A (en) * | 1985-08-15 | 1987-02-21 | Nec Corp | Formation of high melting point metal silicide |
JPS6272122A (en) * | 1985-09-25 | 1987-04-02 | Nec Corp | High melting point metal silicide formation |
US20060228475A1 (en) * | 2003-05-01 | 2006-10-12 | Wisconsin Alumni Research Foundation | Oxidation resistant coatings for ultra high temperature transition metals and transition metal alloys |
CN1948218A (en) * | 2006-10-19 | 2007-04-18 | 宁夏东方钽业股份有限公司 | High temperature anti oxidation material and high temperature antioxidation coating layer prepared from same |
CN101200372A (en) * | 2006-10-19 | 2008-06-18 | 宁夏东方钽业股份有限公司 | High-temperature oxidation-resistant material and high-temperature anti-oxidation coating prepared thereby |
CN101200801A (en) * | 2007-12-18 | 2008-06-18 | 中南大学 | Niobic alloy high temperature antioxidation silicide coating and preparation method thereof |
CN102851635A (en) * | 2012-09-20 | 2013-01-02 | 河北联合大学 | Mo-C-N-Si-Nb gradient coating material and preparation method thereof |
CN104120426A (en) * | 2014-07-25 | 2014-10-29 | 北京航空航天大学 | Mo-Si-B coating on niobium-based alloy and preparation method of Mo-Si-B coating |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105112915A (en) * | 2015-04-30 | 2015-12-02 | 宁夏东方钽业股份有限公司 | Oxidation-resistant material and method employing same for preparing tantalum-tungsten alloy anti-oxidation coating |
CN104928613A (en) * | 2015-06-05 | 2015-09-23 | 柳州弘天科技有限公司 | Preparation method for machining cutter |
CN104947031A (en) * | 2015-06-05 | 2015-09-30 | 柳州弘天科技有限公司 | Manufacturing method of mechanical machining tool |
CN105290389B (en) * | 2015-11-13 | 2018-02-06 | 航天材料及工艺研究所 | A kind of micro-satellite cluster thrust chamber slurry and its preparation method and application |
CN105458269A (en) * | 2015-12-01 | 2016-04-06 | 南通大学 | Manufacturing method of wear-proof coating |
CN106048488A (en) * | 2016-06-21 | 2016-10-26 | 西安理工大学 | Method of preparing high-temperature oxidation-resistant coating on surface of refractory metal material |
CN106048488B (en) * | 2016-06-21 | 2019-05-24 | 西安理工大学 | A method of high-temperature oxidation resistant coating is prepared on refractory metal material surface |
CN107841705A (en) * | 2017-11-09 | 2018-03-27 | 段占娥 | A kind of method for preparing anti-oxidant refractory metal coating |
CN113308689A (en) * | 2021-05-14 | 2021-08-27 | 宁夏东方钽业股份有限公司 | Novel niobium-tungsten alloy high-temperature oxidation-resistant coating material and preparation method thereof |
CN114182251A (en) * | 2021-11-09 | 2022-03-15 | 北京神箭空天科技有限公司 | High-temperature protective coating for jet pipe of aerospace vehicle engine and preparation method and application thereof |
CN114182251B (en) * | 2021-11-09 | 2023-09-12 | 北京神箭空天科技有限公司 | High-temperature protective coating for jet pipe of aerospace vehicle engine as well as preparation method and application thereof |
CN113913723A (en) * | 2021-12-14 | 2022-01-11 | 矿冶科技集团有限公司 | Micron-sized porous-structure thermal barrier coating powder and preparation method thereof |
CN114672805A (en) * | 2022-04-29 | 2022-06-28 | 中北大学 | Preparation method of high-temperature oxidation resistant coating on surface of niobium alloy |
CN114672805B (en) * | 2022-04-29 | 2024-01-30 | 中北大学 | Preparation method of high-temperature oxidation resistant coating on surface of niobium alloy |
CN116253569A (en) * | 2023-01-04 | 2023-06-13 | 河南省科学院碳基复合材料研究院 | Preparation of (Hf, ta) B by using self-propagating auxiliary solid solution doping technology 2 -MoSi 2 Method for preparing oxygen-resistant coating |
CN116253569B (en) * | 2023-01-04 | 2023-12-01 | 河南省科学院碳基复合材料研究院 | Preparation of (Hf, ta) B by using self-propagating auxiliary solid solution doping technology 2 -MoSi 2 Method for preparing oxygen-resistant coating |
Also Published As
Publication number | Publication date |
---|---|
CN104561882B (en) | 2017-01-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104561882B (en) | High-temperature oxidation resistant coating on niobium alloy surface and preparation method of high-temperature oxidation resistant coating | |
CN106435319B (en) | Tungsten-copper alloy and preparation method thereof | |
CN104451655A (en) | Surface alloy coating composite material for high temperature-resistant material, coating and preparation method of coating | |
CN108034939B (en) | A kind of densifying method of Wolfram rhenium heat electric couple high-temperature oxidation resistant coating | |
CN107056334A (en) | A kind of ZrC ceramic material surfaces ZrB2The preparation method of SiC composite coatings | |
CN110140442B (en) | A kind of manufacturing process of compound WZr alloy fragmentation containing energy | |
CN105036556A (en) | Acid resistant enamel slip, and method using slip to make enamel product | |
CN102825259A (en) | Method for preparing TiAl inter-metallic compound powder by using titanium hydride powder | |
CN112877559B (en) | Multi-component ultrahigh-entropy light-weight refractory composite material | |
CN105386041B (en) | A kind of method that laser melting coating prepares modified compound Hf Ta metal coatings | |
US20210278142A1 (en) | Double-shell phase change heat storage balls and preparation method thereof | |
CN106746666A (en) | Glass ceramics composite thermal barrier coating designs a model and coating production | |
CN109943755B (en) | Preparation method of aluminum-based composite material for electronic packaging | |
CN102653470A (en) | Cr2AlC ceramic target and preparation method thereof by vacuum hot pressing | |
CN108396278A (en) | Long-life MCrAlY coating, preparation method and application in hot-end part | |
CN101624662B (en) | Method for preparing W-Cu alloy in microwave infiltration way | |
CN108296491A (en) | A kind of spherical iridium raw powder's production technology of micron order | |
CN102815928B (en) | Preparation method of rare earth ions-doped hexaaluminate high-emissivity material | |
JPH0559195B2 (en) | ||
CN103276266A (en) | Method for preparing TZM alloy material through spray drying | |
CN104276837A (en) | Metal vitrification sealing method | |
CN108034857A (en) | A kind of titanium fire preventing flame retardant coating and preparation method thereof | |
CN108213763A (en) | A kind of Zr bases solder and soldering processes connected for core SiC ceramic | |
CN109112460B (en) | Preparation method of thermal spraying high-temperature-resistant ceramic coating | |
CN110872713B (en) | Y/Y2O3Cold spraying preparation method of metal ceramic protective coating |
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: 20170111 Termination date: 20200130 |