high temperature coatingshome.agh.edu.pl/~grzesik/functional_mater/functional_w2.pdf ·...
TRANSCRIPT
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HIGH TEMPERATURE COATINGS
Zbigniew Grzesik
Department of Physical Chemistry and Modelling
http://home.agh.edu.pl/~grzesik
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Plan of presentation
1) Fundamental definitions2) Fabrication of coatings3) High temperature coatings in corrosion
processes:• oxidizing atmosphere• sulphidizing atmosphere• oxidation-sulphidizing atmosphere• strongly carburizing atmosphere4) Thermal barrier coatings (TBC)5) Summary
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DEFINITIONS
The coating is the thin outer layer of the object, which physiochemical properties and/or structure are different from those of the coated material.
The high temperature coating is the outer layer of a material that provides the protection against corrosion.
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REFERENCES
1. Developments in high-temperature corrosion and protection
of materials. Ed. Wei Gao, Zhengwei Li. Woodhead
Publishing Ltd. Cambridge, England, 2008.
2. High-temperature oxidation of metals. N. Birks, G.H. Meier,
F.S. Pettit. Cambridge University Press. New York, USA
2008.
3. Corrosion: Fundamentals, Testing and Protection. ASM
Handbook, vol. 13A. ASM International. Ohio Park, USA,
2003.
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METHODS OF COATINGS FABRICATION
1. Electrolytic method
2. Chemical methods
3. Immersion method
4. Thermal spraying
5. Diffusion methods
6. Platering
7. Vacuum deposition of electroless method
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THE SURFACE PREPARATION METHODS OF STEEL FOR COATINGS
1. Mechanical methods:- abrasing and/or polishing,- brushing
2. Physico-chemical methods: - degreasing in solvents - emulsion degreasing, - alkaline degreasing, - etching in acids and bases (removing of oxides
and hydroxides) - electrolytic degreasing, - degreasing using ultrasounds
3. Thermal methods – flame desurfacing.
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ELECTROLYTIC COATINGS (GALVANIC)
Electrolytic metal coatings produced on the conductive substrate are obtained by deposition of metals from a solution of their salts or anodes made from appropriate metal, using electric current. The coated object is the cathode and the anode constitutes the plating material.Coatings are obtained in the first stage by the formation of crystallization centers, which subsequently grow to form a continuous layer with required thickness.Factors affecting the properties of the coatings: the type of metal substrate, type and concentration of additives (eg, increasing the electrical conductivity of the bath, causing the formation of finely coating or brightening shell), current density, bath temperature, time of the process and methods of mixing the bath (mechanical, compressed air, etc.).
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CHEMICAL COATINGS
Chemical (electroless) imposition of metals involves the reduction of metal compounds from solutions of their salts by using reducers (hypophosphoric acid salts, or other). Until now chemical methods are developed, consisting in chemical vapor deposition of nickel, cobalt, tin, copper, silver, gold, palladium or platinum. The contact coating method consists in displacement of the metal ions from solution by the metal substrate.Metallic coatings deposited by chemical methods are rarely used for protection against high temperature corrosion.
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HOT-DIP COATINGS (IMMERSION)
Hot-dip coatings are obtained by immersion of a given material in a molten metal bath. This method is the oldest and cheapest one, currently utilized in obtaining metallic coatings, well adherent to the substrate.This method is mainly used in those cases when the material shows considerable length (tapes, wires). This method can be applied only when the melting point of a given material is higher then that of the coating. In practice, this method is used for coating tin (232°C), lead (327°C), zinc (419°C) and aluminum (660°C).
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HOT–DIP COATING (DIP COATING)
- scheme of device for hot-dip tinning
1 – oil, 2 - cylinder head, 3 – fluxing agent, 4 - molten tin
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THERMAL SPRAY COATINGS
Thermal metal spraying involves melting, using different heat sources (flame, electric arc, plasma arc or high-frequency current). The metal for coating production is used in the form of wire or powder, which after melting is directed to the substrate in a stream of compressed gas (usually air). In the high temperature flame or arc, metal particles are partially oxidized, and after hitting the ground are flattened. During hitting of the ground the oxide thin film is cracking and consequently the coating constitutes a shell of sprayed metal, its oxide and pores. The total pore volume generally does not exceed 15%.
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THERMALLY SPRAYED COATINGScheme formation of the sprayed metal layer
1 - oxide on particle film, 2 - the liquid inside the particle, 3 - particle splash during impact,4 - rest of the oxide film between sprayed particles, 5 - jamming the particles,6 - particles coupled by mutual welding, 7 - particle at low temperature (not plastic),8 - the gap between the particles (not plastic), 9 - micropores (developed due to traped of exhaust gas between particles, 10 - surface of the substrate, 11 - substrate
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DIFFUSION COATINGS
Diffusion coatings are produced by changing the chemical composition of the surface layer of a given material as a result of the introduction of alien elements. Diffusion coating is a part of the substrate material saturated with alien elements, which cannot be separated from it. Metals plated on the substrate surface diffuse into the crystal lattice, not influencing the apparent changes of its dimensions.
Typical diffusion processes:
• Aluminizing• Chrome plating• Chrome aluminizing• Galvanizing• Chrome siliconizing
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PLATING
Plating method consists in mechanical coating of a relatively thick layers of a given metal on protected substrate, being in the form of tape or wire. Metal coating (more noble or more decorative) can be obtained by casting, welding, soldering, rolling or explosive plating. The penetration of the coating metal into the substrate proceeds under the influence of pressure and temperature, providing the welding. Carbon steels are usually plating by copper, nickel, aluminum and acid resistant steels.
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METHOD OF EXPLOSIVE PLATING
a) planar system, b) cylindrical system; 1 – explosive material2 – detonator, 3 – material applied as a coating, 4 – substrate
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VACUUM DEPOSITION COATINGS
Methods of vacuum deposition of metals:• Electroless vacuum deposition • Cathodic sputtering• Ionic metallization
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PROTECTIVE COATINGS APPLIED IN THE CASE OF CORROSION
OCCURRING IN OXIDIZING ATMOSPHERES
Cr – Cr2O3
Al – Al2O3
Si – SiO2
MCrAlY (where M = Co, Ni, Co/Ni) – Al2O3, Cr2O3
MCrAlY-Si – Al2O3, Cr2O3
MCrAlY-RE (where RE = Y, Hf, Zr) – Al2O3
NiAl – Al2O3
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Ni-Al phase diagram
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Cross-section of the Ni-Cr-Al-Y coating obtained by the EB-PVD method
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Surface and cross-section of the Co-Cr-Al-Y coatingobtained by the EB-PVD method on the IN-738 alloy
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PROTECTIVE COATINGS APPLIED IN CORROSIONOCCURRING IN SULPHIDIZING ATMOSPHERES
Mn – MnS
Ti – TiS2
Mo – MoS2
Nb – NbS2
Ta – TaS2
Ni-Mo, Fe-Mo, Co-Mo
Fe-Mo-Al
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Comparison of sulphidation and oxidation rates of several alloys
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Sulphidation rates of several Ni and Fe alloys containing Mo and Al
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PROTECTIVE COATINGS UTILIZED IN THE CASE OF OXIDIZING-SULPHIDIZING ATMOSPHERES
Fe-Mo-Al
Mo-Al
Mo-Al-Si
Nb-Al
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Cross-section of scales formed on a superalloy in oxidizing and oxidizing-sulphidizing atmospheres
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Environment
Oxide
Alloy
Men+
Men+
Men+
Men+Men+Men+
Men+
S
SS
S S
S
S S S
S
SS
S SSS
S S S
S
S
Sulphide
Sulphide
S
(a) (b) (c)
(d) (e) (f)
(g) (h) (i)
Environment
Oxide
Alloy
Environment
Oxide
Alloy
Scheme of degradation of materials in the oxidizing-sulphidizing atmospheres
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Sulphidizing rates of high-temperature alloys containing aluminum
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Sulphidizing rates of Mo-Al alloys
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X-ray data of the Al-34Mo alloy
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Cross-section of sulphide scalegrowing on the Al-46Mo alloy
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Comparison of the sulphidizing and oxidizing rates of several alloys
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Comparison of the oxidizing rates of several Al-Mo-Si alloys
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The molybdenum content in scalesgrowing on several Al-Si-Mo alloys
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Comparison of the sulphidizing kinetics of two Al-Mo alloyswith different Si contents
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Comparison of the sulphidizing and oxidizing rates of several alloys
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Comparison of the sulphidizing rates of several alloys
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The result of X-ray analysis of Al-54Nb-20Si alloy
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CONCLUSION
Protective coatings against high temperature corrosion in oxidizing-sulphidizing environments have not been elaborated.
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Coatings in the protection against corrosion at highly carburizing atmospheres
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The mechanism of a metal-dusting corrosion of iron and low-alloy steels
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5 0 m
Typical corrosive destructions
low-alloy steel
alloyed steel
5 0 m
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Typical corrosive destructions
2 c m 2 c m
1 c m
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Typical corrosive destructions
2 c m 2 c m
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10 mm
The 9Cr-1MO steel sample after 3 hours reaction in propane-butane atmosphere at a temperature of 1173 K
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The mechanism of a metal-dusting corrosion of high alloyed steels
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CONCLUSION
In spite of long-term studies of metal dusting corrosion, no rational basis has been created for decreasing the rate of this form of high temperature corrosion. Further studies are required to control this detrimental phenomenon.
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Thermal barrier coatings (TBC)
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Scheme of a typical TBC system
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Cross-sections of TBC coatings
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Surface and cross-sections of a layer of TBC protective coating after oxidation
EB-PVD YSZ TBC
Pt-modified bond coat
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Cross sections of a layer of TBC protective coating after oxidation
EB-PVD YSZ TBC
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Cross section of four-cylinder in-line engine with spark ignition, Fiat
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The results of oxidation of X33CrNiMn23-8 steel under thermal shock conditions
Number of thermal shocks
Time /h
1 cycle = 2h
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The results of oxidation of X50CrMnNiNbN21-9 steel under thermal shock conditions
Number of thermal shocks
Time /h
1 cycle = 2h
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Images of sample surfaces of X33CrNiMn23-8 steels under thermal shock conditions at 1173 K
50 cycles 100 cycles
500 cycles250 cycles
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The photographs of surfaces of uncovered X50CrMnNiNbN21-9 steel sample
after different thermal shock numbers
300 cycles 500 cycles
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Surface layer of the TBC
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s t e e l
i n n e r l a y e r o f t h e c o a t i n g
o u t e r l a y e r o f t h e c o a t i n gZrO2Y2O3
Ni22Cr10AlY
Cross-section of a layer of TBC coating deposited on steel
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6 7 8 9 10 1110-7
10-6
10-5
10-4
10-3
10-2
10-1
.T-1
104 / K
-1
k p
/ g2 m
-4s-1
1573 1373 1173 973
chromia formersalumina formers
coated steel
-NiAl
Fe-5Cr-4Al Ni-10Cr-5Al
Ni-30Cr
Fe-20Cr
steel
Co-35Cr
Oxidation
T / K
Temperature dependence of the oxidation rate of steel coated with a protective coating
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The results of oxidation of X50CrMnNiNbN21-9 steel coated with a protective coating under thermal shock conditions
Number of thermal shocks
Time /h
1 cycle = 2h
coating
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The results of oxidation of X33CrNiMn23-8 steel coated with a protective coating under thermal shock conditions
Number of thermal shocks
Time /h
1 cycle = 2hcoating
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0 100 200 300 400 5000
5
10
15
coated X33CrNiMn23-8 steel
Number of thermal shocks
m
/S 1
04 /
g cm
-2
coated X50CrMnNiNbN21-9 steel
1 cycle = 2 h
.
0 200 400 600 800 1000
Time / h
The results of oxidation of two valve steels coated with a protective coating under thermal shock conditions
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The photographs of the surface sample of X33CrNiMn23-8 steelcovered with hybrid coating in 1173 K
before oxidation after 500 cycles
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The influence of yttrium on kinetics of chromia scale growth on Fe-Cr-Ni base steels
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EXPERIMENTALMaterials:
X33CrNiMn23-8, X50CrMnNiNbN21-9, X53CrMnNiN20-8, X55CrMnNiN20-8
Specimens:
• discs: diameter 20 mm, thickness 1 mm• weight: 1 g
Yttrium deposition:
• degreasing• electrochemical treatment: 0.01 m Y(NO3)3 solution in C2H5OH
U = 10V; I = 10 mA; t = 45 s• drying: T = 50 oC; t = 10 min.• annealing: T = 400 oC; t = 30 min.
Corrosion tests under thermal shock conditions:
•reactive atmosphere: combustion gases of diesel oil with 10 wt. % addition of FAME (B10)•temperature range: 295 – 1173 K •time of experiments: 150 shocks x 2 h, quenching cycle: 15 min.
SEM, EDX, XRD EXAMINATION
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Corrosion behaviour of the X33CrNiMn23-8 steel uncovered and covered with yttrium under
thermal shock conditions
0 50 100 150-0.06
-0.05
-0.04
-0.03
-0.02
-0.01
0.00
steel with Y
steel without Y
T = 1173 K
X33CrNiMn23-8 steel
m
/S
/ g c
m-2
Number of thermal shocks
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Corrosion behaviour of the X50CrMnNiNbN21-9 steel uncovered and covered with yttrium under thermal
shock conditions
0 50 100
-0.3
-0.2
-0.1
0.0
1 cycle = 2h
X50CrMnNiNbN21-9 steel
steel with Y
steel without Y
T = 1173 K
m
/S
/ g c
m-2
Number of thermal shocks
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Corrosion behaviour of the X53CrMnNiN20-8 steel uncovered and covered with yttrium under thermal
shock conditions
0 50 100-0.3
-0.2
-0.1
0.0X53CrMnNiN20-8 steel
1 cycle = 2h
steel with Y
steel without Y
T = 1173 K
m
/S
/ g c
m-2
Number of thermal shocks
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Corrosion behaviour of the X55CrMnNiN20-8 steel uncovered and covered with yttrium under thermal
shock conditions
0 50 100
-0.2
-0.1
0.0X55CrMnNiN20-8 steel
1 cycle = 2h
steel with Y
steel without Y
T = 1173 K
m
/S
/ g c
m-2
Number of thermal shocks
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The photographs of surfaces of steel samples coated with yttrium after 100 thermal shocks
a) X33CrNiMn23-8; b) X50CrMnNiNbN21-9; c) X53CrMnNiN20-8; d) X55CrMnNiN20-8
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Conclusion
The results of thermal shock experiments have demonstrated that small amounts of yttrium electrochemically deposited on the surface of the X33CrNiMn23-8 steel, containing highest chromium concentration (> 23 wt. %), dramatically improves the chromia scale adherence to the surface of this steel, due to selective oxidation of chromium and formation of Cr2O3 oxide. This effect is not observed in the case of three remaining steels with lower chromium concentration, because of heterogeneous scale formation. From practical point of view, it may be then concluded that engine valves should be produced in the future only from X33CrNiMn23-8 steel covered by yttrium.
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SUMMARY
Up to now, no universal coatings for high temperature applications have been elaborated.
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THE END