CN111872372B - Coating powder composition and method for preparing coating - Google Patents

Coating powder composition and method for preparing coating Download PDF

Info

Publication number
CN111872372B
CN111872372B CN202010773476.4A CN202010773476A CN111872372B CN 111872372 B CN111872372 B CN 111872372B CN 202010773476 A CN202010773476 A CN 202010773476A CN 111872372 B CN111872372 B CN 111872372B
Authority
CN
China
Prior art keywords
powder
coating
parts
powder composition
composition
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
CN202010773476.4A
Other languages
Chinese (zh)
Other versions
CN111872372A (en
Inventor
赵刚
周小军
刘尖
梁斌
王立斐
任广宁
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.)
Ningxia Orient Tantalum Industry Co Ltd
Original Assignee
Ningxia Orient Tantalum Industry Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ningxia Orient Tantalum Industry Co Ltd filed Critical Ningxia Orient Tantalum Industry Co Ltd
Priority to CN202010773476.4A priority Critical patent/CN111872372B/en
Publication of CN111872372A publication Critical patent/CN111872372A/en
Application granted granted Critical
Publication of CN111872372B publication Critical patent/CN111872372B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • B22F1/0003
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • B22F1/103Metallic powder containing lubricating or binding agents; Metallic powder containing organic material containing an organic binding agent comprising a mixture of, or obtained by reaction of, two or more components other than a solvent or a lubricating agent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • B22F2009/041Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling by mechanical alloying, e.g. blending, milling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Powder Metallurgy (AREA)

Abstract

The present invention relates to a coating powder composition comprising: mo powder, W powder, Y2O3Powder, Cr powder, V powder, Ta powder, B powder, ZrB powder2Powder, KF powder, Ir powder, carbide powder, MoSi2Powder, Si powder, wherein carbide is selected from one or more of SiC and NbC; wherein the coating powder composition does not contain Ti and Hf.

Description

Coating powder composition and method for preparing coating
Technical Field
The invention belongs to the field of surface treatment, and particularly relates to a coating powder composition and a method for preparing a coating.
Background
The aerospace and aviation aircraft engines, structural members and control functional elements need to be used in a high-temperature oxidation environment, and fasteners which can simultaneously have high melting point, high room-temperature mechanical property, strong oxidation resistance and low density requirements are needed so as to meet the special light and high-strength use requirements of aerospace and aviation. In addition, the industries of steel, chemical industry, metallurgy and the like have a plurality of high-temperature operation processes, and similar fasteners with high-temperature resistance, high room-temperature mechanical property and oxidation resistance are also needed.
At present, the fastening piece materials at home and abroad mostly use titanium, iron, cobalt and nickel-based alloys, and the use temperature of the materials cannot exceed 1200 ℃ due to the limitation of the melting point of the materials. The ceramic material has poor processing performance, insufficient mechanical property at shearing room temperature and extremely limited application. Noble metals have good oxidation resistance, but have high cost and insufficient mechanical properties at high temperature and room temperature, and are greatly limited in practical application.
Tantalum and niobium have the advantages of high melting point, good processing performance and relatively low cost, and have important application in the high-temperature field, and the typical application is that tantalum or niobium is used as connecting pieces such as screws or rivets when a heating body of a high-temperature resistance furnace is manufactured. However, tantalum and niobium have poor oxidation resistance, and therefore, when used at high temperature, vacuum and inert gas protection are required, or a coating is applied on the surface.
When the Cr-Ti-Si series coating is coated on the Nb-752 alloy, the oxygen content in the Nb-752 alloy is reduced, and the mechanical property of the alloy at room temperature is further reduced. When the coating is coated on the surface of a fastener, the mechanical property of the fastener at room temperature is reduced, and the phenomenon of slide-fastening occurs during assembly or use, so that the pretightening force of the fastener is reduced or completely damaged, and the use safety and reliability of the fastener are seriously influenced.
Disclosure of Invention
Through a great deal of research and development work, the inventor discovers a novel coating powder composition, and a coating prepared by using the coating powder composition is coated on a substrate, so that the novel coating powder composition has the advantages of high temperature resistance and oxidation resistance. Moreover, the mechanical properties of the substrate are not reduced by the coating.
In some aspects, the present disclosure provides a coating powder composition comprising, by weight:
3-8.0 parts of Mo powder;
2.0-3.5 parts of W powder;
50-80 parts of Si powder;
0.1-2.5 parts of Ta powder;
2.0-8.5 parts of Cr powder;
Y2O30.1-2.0 parts of powder;
3-6.0 parts of V powder;
0.5-1.5 parts of powder B;
2.7-4 parts of carbide powder;
ZrB20-1.5 parts of powder;
0-1 part of KF powder;
0.5-3 parts of Ir powder;
MoSi26-8 parts of powder; (e.g., 7 parts) and
0.5-3 parts of Ir powder;
wherein the carbide is selected from one or more of SiC and NbC;
wherein the coating powder composition does not contain Ti and Hf.
Based on the technical scheme, the coating powder composition disclosed by the invention contains carbide (such as selected from SiC and NbC), so that the concentration of C in the coating is higher, and the condition that C in a matrix diffuses into the coating to cause the reduction of the room-temperature mechanical property of the alloy is effectively avoided.
Based on the technical scheme, the coating powder composition disclosed by the invention does not contain metal elements such as Ti, Hf and the like which have an absorption effect on strengthening elements (such as C and/or O elements) in the matrix. For example, the coating powder composition does not contain Ti simple substance, alloy or compound, Hf simple substance, alloy or compound. The mechanical property of the substrate is not reduced by coating the coating.
In some embodiments, the carbide powder is SiC powder, and the SiC powder is present in an amount of 3 to 4 parts.
In some embodiments, the carbide powder is a mixture of NiC powder and SiC powder, the SiC powder is present in an amount of 2 to 3 parts, and the NbC powder is present in an amount of 0.5 to 1 part.
In some embodiments, the parts by weight are based on 100 parts of the coating powder composition.
In some embodiments, parts by weight refers to parts by weight percent, parts of each component refers to percent by weight.
In some embodiments, the weight percent of each ingredient in the coating powder composition is a percentage relative to the total weight of the coating powder composition.
In some embodiments, the powder particle size of the coating powder composition is 200 mesh or less. The product can pass through 200 mesh sieve below 200 mesh.
In some aspects, there is provided a coating slurry comprising:
the above coating powder composition;
a binder; and
a liquid carrier;
wherein the weight ratio of the binder to the powder composition is 1.2-5: 100, respectively;
wherein the volume ratio of the liquid carrier to the powder composition is 0.5-2: 1 (e.g., 1: 1);
preferably, the binder is polyethylene glycol having a molecular weight of 5000-.
In some aspects, the present disclosure provides a method of preparing a coating slurry, comprising the steps of:
(1) mixing the coating powder composition of any one of the above with a binder and a liquid carrier;
(2) grinding (such as ball milling) the product obtained in the last step;
preferably, in the step (1), the weight ratio of the binder to the powder composition is 1.2-5: 100, respectively;
preferably, the volume ratio of the liquid carrier to the powder composition is 0.5-2: 1;
preferably, in step (1), the binder is polyethylene glycol with a molecular weight of 5000-.
In the scheme, the grinding has the pre-alloying effect, and the C element with a certain content is uniformly distributed in the coating through pre-alloying, so that the C element is prevented from diffusing from the substrate to the coating.
In some aspects, the present disclosure provides a coating slip prepared by the method of any one of the above.
In some aspects, the present disclosure relates to a method of preparing a coating on a substrate, comprising the steps of:
(1) coating the coating slurry on the surface of a substrate;
(2) and sintering the product of the last step.
In some embodiments, the sintering is performed in a vacuum environment.
In some embodiments, the temperature of sintering is 1500-1600 ℃.
In some embodiments, the coating has a thickness of 50 to 100 μm
In some embodiments, the substrate is a tantalum alloy or a niobium alloy.
In some embodiments, the substrate is a niobium tungsten alloy.
In some embodiments, the niobium tungsten alloy has the following composition: 4.5 to 5.5 wt% of W, 1.7 to 2.3 wt% of Mo, 0.7 to 1.2 wt% of Zr, 0.05 to 0.12 wt% of C, and the balance of Nb and inevitable impurities.
In some aspects, the present disclosure provides a coated component prepared by the method of any one of the above.
In some embodiments, the coating powder composition comprises Mo powder, W powder, Si powder, Ta powder, Cr powder, Y powder2O3Powder, V powder, B powder, carbide powder, ZrB2Powder, KF powder, Ir powder, MoSi2The sum of the weights of the powders is 100% or less of the total weight of the coating powder composition. The coating powder composition may also contain a binder, an additive, an auxiliary material, and the like.
In some embodiments, the sum of the components in the coating powder composition is 100%.
Interpretation of terms
"comprising", "containing" and "containing" have the same meaning, i.e.a content of more than zero, for example ≥ 0.1 wt.%, for example ≥ 1 wt.%, for example ≥ 10 wt.%, for example ≥ 20 wt.%, for example ≥ 30 wt.%, for example ≥ 40 wt.%, for example ≥ 50 wt.%, for example ≥ 60 wt.%, for example ≥ 70 wt.%, for example ≥ 80 wt.%, for example ≥ 90 wt.%, for example 100 wt.%. The meaning of "comprising", "containing" or "containing" is equivalent to "consisting of …" when the content is 100 wt% "
"free" may mean substantially free, e.g., less than 0.1 wt%, e.g., less than 0.01 wt%, e.g., less than 0.001 wt%.
"powder" means particles that pass through an N mesh screen. The value of N may be 10 or more, for example 100 to 1000, for example 200 to 600.
Advantageous effects
(1) The mechanical property of the coating at room temperature of the alloy is basically not influenced, the tightening torque of the coating fastener is almost consistent with that before the coating, and the phenomenon of slipping is avoided;
(2) the coating has oxidation resistance (the oxidation resistance life is more than or equal to 2h at 1600 ℃ and the water-cooling thermal shock performance at 1600-room temperature is more than or equal to 200 times), and can play a good role in oxidation resistance protection for the fastener.
Drawings
FIG. 1 is a schematic view of an embodiment NbW5-1 alloy fastener.
FIG. 2 is a schematic diagram of an assembly-tension test of one embodiment.
Detailed Description
The formulations of the coating powder compositions used in the following examples are shown in Table 1. The particle size of each component powder is 200 meshes.
TABLE 1
Figure BDA0002617512280000051
Figure BDA0002617512280000061
COMPARATIVE EXAMPLE 1 (blank)
NbW5-1 alloy fasteners are provided, which are M8 size bolts. FIG. 1 shows a schematic view of an NbW5-1 alloy fastener. The NbW5-1 alloy had a composition of 91.5Nb-4.87W-1.93Mo-0.84Zr-0.064C (wt%).
As shown in fig. 1, the fastener is a bolt 10, the bolt 10 having an external thread 11.
Comparative example 1 also provided a co-fired coupon of the NbW5-1 alloy fastener.
Example 1
1) Coating powder compositions were formulated according to the formulation shown in table 1 and then placed in a container;
2) adding anhydrous ethanol with the volume 1 time that of the powder composition into a container as a carrier;
3) adding polyethylene glycol as a binder in an amount of 1.2 wt% based on the mass of the powder composition into a container;
4) the materials are ball-milled at a high speed to prepare slurry, the ball-milling speed is 150r/min, and the ball-milling time is 10 hours;
5) the fasteners (blank samples) made of the NbW5-1 alloy of the comparative example 1 are all immersed in the slurry for 5s and then taken out, and are dried for 10min in a ventilated environment;
6) and (3) placing the fastener with the slurry coated on the surface into a vacuum resistance furnace, sintering in a high-temperature and vacuum environment (1550 ℃ and below 0.1 Pa), and forming a high-temperature-resistant and oxidation-resistant coating on the surface after sintering. The thickness of the coating is 55 to 68 μm.
The same coating treatment was carried out on test pieces of NbW5-1 alloy fasteners as in the furnace.
Example 2
1) Coating powder compositions were formulated according to the formulation shown in table 1 and then placed in a container;
2) adding anhydrous ethanol with the volume 1 time that of the powder composition into a container as a carrier;
3) adding polyethylene glycol (molecular weight 6000) as a binder in an amount of 5 wt% based on the mass of the above powder composition into a container;
4) the materials are ball-milled at a high speed to prepare slurry, the ball-milling speed is 450r/min, and the ball-milling time is 3.5 h;
5) all the fasteners (blank samples) made of the NbW5-1 alloy of the comparative example 1 are immersed in the slurry for 10s and then taken out, and the fasteners are dried for 45min in a ventilated environment;
6) and (3) placing the fastener with the slurry coated on the surface into a vacuum resistance furnace, sintering in a high-temperature and vacuum environment (1550 ℃ and below 0.1 Pa), and forming a high-temperature-resistant and oxidation-resistant coating on the surface after sintering. The thickness of the coating is 57-65 μm.
The same coating treatment was carried out on test pieces of NbW5-1 alloy fasteners as in the furnace.
Analytical testing
1. Mechanical properties
The NbW5-1 alloy fasteners of comparative example 1, and example 2 were tested for mechanical properties according to the test standard, GJB715.23 "tensile strength of fastener test method", and the results are shown in table 2 below.
TABLE 2
Figure BDA0002617512280000071
2. Oxidation resistance test
The oxidation resistance test was performed on the same furnace test pieces of examples 1 and 2, and the test piece specification: 70X 8X 1 (mm). The test comprises a static oxidation test at 1600 ℃ and a water-cooling thermal shock test at 1600 ℃ -room temperature, and a high-temperature oxidation tester is adopted for detection according to the industry standard. The test results are shown in table 3 below.
TABLE 3
Figure BDA0002617512280000072
Figure BDA0002617512280000081
3. Assembly-tensile test
The coated fasteners of the embodiment 1 and the comparative example 1 are disassembled and assembled at normal temperature with a torque wrench and the matched nut, and the non-brand new fastener is obtained after repeated disassembly and assembly.
The non-new fastener described above is installed into the tension clamp shown in fig. 2. The tension jig includes an upper jig 21 and a lower jig 22, the upper jig 21 fixing the head of the bolt 10, and the lower jig 22 fixing the shank of the bolt 10. The lower clamp 22 is made of a C/SiC composite material. The lower clamp 22 has an internal thread 24, the internal thread 24 cooperating with the external thread 11 of the bolt 10. The arrows in fig. 2 show the load loading direction, pulling the upper clamp 21 and the lower clamp 22 in opposite directions until the external thread 11 slips with the internal thread 24.
The test results are shown in table 4 below:
TABLE 4
Figure BDA0002617512280000082
The experimental data in tables 2 to 4 show that the coating prepared from the coating powder composition of the present invention is used for preparing a high temperature resistant and oxidation resistant coating, which has the following advantages:
(1) the mechanical property of the coating at room temperature of the alloy is basically not influenced, the tightening torque of the coating fastener is almost consistent with that before the coating, and the phenomenon of slipping is avoided;
(2) the coating has oxidation resistance (the oxidation resistance life is more than or equal to 2 hours at 1600 ℃ and the water-cooling thermal shock performance at 1600-room temperature is more than or equal to 200 times), and can play a good role in oxidation resistance protection for the fastener;
(3) the coating has better durability and still has better tensile property after repeated assembly.
Although embodiments of the invention have been described in detail, it will be appreciated by those skilled in the art that various modifications and alternatives to those details could be developed in light of the overall teachings of the disclosure, and that such modifications are intended to be within the scope of the invention. The full scope of the invention is given by the appended claims and any equivalents thereof.

Claims (14)

1. A coating powder composition comprising, in parts by weight:
3-8.0 parts of Mo powder;
2.0-3.5 parts of W powder;
50-80 parts of Si powder;
0.1-2.5 parts of Ta powder;
2.0-8.5 parts of Cr powder;
Y2O30.1-2.0 parts of powder;
3-6.0 parts of V powder;
0.5-1.5 parts of powder B;
2.7-4 parts of carbide powder;
ZrB20-1.5 parts of powder;
0-1 part of KF powder;
0.5-3 parts of Ir powder; and
MoSi26-8 parts of powder;
wherein the carbide is selected from one or more of SiC and NbC;
wherein the coating powder composition does not contain Ti and Hf.
2. The coating powder composition of claim 1, wherein:
the carbide powder is SiC powder, and the content of the SiC powder is 3-4 parts by weight; or
The carbide powder is a mixture of NbC powder and SiC powder, and the content of the SiC powder is 2-3 parts by weight and the content of the NbC powder is 0.5-1 part by weight.
3. The coating powder composition according to claim 1, wherein the powder particle size of the coating powder composition is 200 mesh or less.
4. The coating powder composition of claim 1, wherein the parts by weight are based on 100 parts of the coating powder composition.
5. A coating slip comprising:
the coating powder composition of any one of claims 1 to 4;
a binder; and
a liquid carrier;
the weight ratio of the binder to the coating powder composition is 1.2-5: 100, respectively;
the volume ratio of the liquid carrier to the coating powder composition is 0.5-2: 1;
the binder is polyethylene glycol with molecular weight of 5000-10000.
6. A method of preparing a coating slurry comprising the steps of:
(1) mixing the coating powder composition of any one of claims 1 to 4 with a binder and a liquid carrier;
(2) grinding the product obtained in the previous step;
in the step (1), the weight ratio of the binder to the coating powder composition is 1.2-5: 100, respectively;
the volume ratio of the liquid carrier to the coating powder composition is 0.5-2: 1;
in the step (1), the binder is polyethylene glycol with the molecular weight of 5000-10000.
7. The method of claim 6, wherein the milling is ball milling, the rotation speed of the ball milling is more than 100-400 r/min, and the ball milling time is more than 3 h.
8. A coating slip obtained by the process of claim 6 or 7.
9. A method of preparing a coating on a substrate comprising the steps of:
(1) applying the coating slip of claim 5 or 8 to a substrate surface;
(2) and sintering the product of the last step.
10. The method of claim 9, characterized by one or more of the following:
-said sintering is carried out in a vacuum environment;
-the temperature of the sintering is 1500-1600 ℃;
the thickness of the coating is 50-100 μm.
11. The method of claim 9, wherein the substrate is a tantalum alloy or a niobium alloy.
12. The method of claim 11, wherein the substrate is a niobium tungsten alloy.
13. The method of claim 12, the niobium tungsten alloy having the following composition: 4.5 to 5.5 wt% of W, 1.7 to 2.3 wt% of Mo, 0.7 to 1.2 wt% of Zr, 0.05 to 0.12 wt% of C, and the balance of Nb and inevitable impurities.
14. A coated component produced by the method of any one of claims 9 to 13.
CN202010773476.4A 2020-08-04 2020-08-04 Coating powder composition and method for preparing coating Active CN111872372B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010773476.4A CN111872372B (en) 2020-08-04 2020-08-04 Coating powder composition and method for preparing coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010773476.4A CN111872372B (en) 2020-08-04 2020-08-04 Coating powder composition and method for preparing coating

Publications (2)

Publication Number Publication Date
CN111872372A CN111872372A (en) 2020-11-03
CN111872372B true CN111872372B (en) 2022-02-22

Family

ID=73211609

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010773476.4A Active CN111872372B (en) 2020-08-04 2020-08-04 Coating powder composition and method for preparing coating

Country Status (1)

Country Link
CN (1) CN111872372B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113308689B (en) * 2021-05-14 2022-07-05 宁夏东方钽业股份有限公司 Niobium-tungsten alloy-Nb 6621 high-temperature oxidation-resistant coating material and preparation method thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0238758A2 (en) * 1986-03-28 1987-09-30 Martin Marietta Corporation Welding using metal-ceramic composites
CN1105918A (en) * 1993-10-27 1995-08-02 H·C·施塔克公司 Method for producing metal and ceramic sintered bodies and coatings
JP2004107558A (en) * 2002-09-20 2004-04-08 Nekken Kagaku Kogyo Kk Heat-resistant and anticorrosive coating and heat-resistant and anticorrosive coating film
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
CN101863683A (en) * 2009-04-15 2010-10-20 中国科学院上海硅酸盐研究所 Anti-oxidation coating and preparation method thereof
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
CN106853436A (en) * 2016-12-29 2017-06-16 宁夏东方钽业股份有限公司 A kind of molybdenum base composite coating and preparation method thereof
WO2017192674A1 (en) * 2016-05-03 2017-11-09 The Government Of The United States Of America, As Represented By The Secretary Of The Navy Refractory metal silicide nanoparticle ceramics
CN111172530A (en) * 2020-01-17 2020-05-19 江苏理工学院 Method for repairing silicide coating on surface of Mo alloy sheet

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160023951A1 (en) * 2013-01-07 2016-01-28 Vince Alessi Thermoset ceramic compositions, inorganic polymer coatings, inorganic polymer mold tooling, inorganic polymer hydraulic fracking proppants, methods of preparation and applications therefore

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0238758A2 (en) * 1986-03-28 1987-09-30 Martin Marietta Corporation Welding using metal-ceramic composites
CN1105918A (en) * 1993-10-27 1995-08-02 H·C·施塔克公司 Method for producing metal and ceramic sintered bodies and coatings
JP2004107558A (en) * 2002-09-20 2004-04-08 Nekken Kagaku Kogyo Kk Heat-resistant and anticorrosive coating and heat-resistant and anticorrosive coating film
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
CN101863683A (en) * 2009-04-15 2010-10-20 中国科学院上海硅酸盐研究所 Anti-oxidation coating and preparation method thereof
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
WO2017192674A1 (en) * 2016-05-03 2017-11-09 The Government Of The United States Of America, As Represented By The Secretary Of The Navy Refractory metal silicide nanoparticle ceramics
CN106853436A (en) * 2016-12-29 2017-06-16 宁夏东方钽业股份有限公司 A kind of molybdenum base composite coating and preparation method thereof
CN111172530A (en) * 2020-01-17 2020-05-19 江苏理工学院 Method for repairing silicide coating on surface of Mo alloy sheet

Also Published As

Publication number Publication date
CN111872372A (en) 2020-11-03

Similar Documents

Publication Publication Date Title
US4668470A (en) Formation of intermetallic and intermetallic-type precursor alloys for subsequent mechanical alloying applications
Chang et al. Superalloy powder processing, properties and turbine disk applications
Garosshen et al. Effects of B, C, and Zr on the structure and properties of a P/M nickel base superalloy
EP0091260B1 (en) Process for preparing an oxide dispersion strengthened high temperature alloy
RU2377336C2 (en) Alloy for gasturbine engine
DE102017101919A1 (en) Wear-resistant and corrosion-resistant cobalt-based alloy powders and their applications
US4668282A (en) Formation of intermetallic and intermetallic-type precursor alloys for subsequent mechanical alloying applications
DE3211583A1 (en) SUPER ALLOY COATING COMPOSITION WITH HIGH-TEMPERATURE OXIDATION RESISTANCE
CN111872372B (en) Coating powder composition and method for preparing coating
US4740354A (en) Nickel-base alloys for high-temperature forging dies usable in atmosphere
US4507264A (en) Nickel base brazing alloy and method
US3720537A (en) Process of coating an alloy substrate with an alloy
CN108728694A (en) Layered component for superalloy articles reparation
EP1956105A1 (en) Alloy, protective layer for protecting a component from corrosion and oxidisation in high temperatures and component
US2977225A (en) High-temperature alloys
CN112853163B (en) High-temperature-resistant aluminum alloy composite material and preparation method thereof
Choo et al. Mechanical properties of NiAl–AlN–Al2O3 composites
US2860970A (en) Metal alloy
US5180446A (en) Oxide-dispersion-strengthened niobum-based alloys and process for preparing
US3309767A (en) Brazing alloy and method of brazing with same
RU2148671C1 (en) Nickel-aluminum-base intermetallic alloy
US2974037A (en) High temperature cobalt base alloy
EP0260465A1 (en) Oxide dispersion-strengthened nickel-base superalloy with improved corrosion resistance
Kaku et al. Hot deformation studies of Al–Cu–Mg powder metallurgy alloy composite
US3254994A (en) Alloys having improved stress rupture properties

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