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Advanced High Temperature Alloys
Prof. Dr.-Ing. Uwe GlatzelgMetals and Alloys
University BayreuthSS 2010
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys1
Lecturer:Lecturer:Prof Dr Ing habil Uwe GlatzelProf. Dr.-Ing. habil. Uwe Glatzel• born Dez. 1960• Physik-Diplom (B Sc and M Sc) in Tübingen• Physik-Diplom (B.Sc. and M.Sc) in Tübingen
(exchange year in Corvallis, Oregon, USA)• PhD thesis at the Institute for Metals Research, Technical
University Berlin, Prof. Monika Feller-Kniepmeier• post-doc (1 Jahr) at Stanford University• Habilitation TU-BerlinHabilitation TU-Berlin• Gerhard-Hess award of the German Science Foundation
(DFG) for young scientist (400.000 €)• 1996-2003 full professor for Metals and Alloys, Jena• since April 2003 Bayreuth (Chair for Metals and Alloys)postal address:
d i h b h ( )
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys2
Ludwig-Thoma-Str. 36b phone: +49 (0) 921 - 55-5555D-95447 Bayreuth, Germany e-mail: uwe.glatzel@uni-bayreuth.de
Literature• R Bürgel Handbuch Hochtemperatur-Werkstofftechnik Vieweg
LiteratureR. Bürgel, Handbuch Hochtemperatur Werkstofftechnik, Vieweg
• R.C. Reed, The Superalloys - Fundamentals and Applications, Cambridge Univ. Press• H. Frost, M. Ashby, Deformation-Mechanism Maps, Pergamon Press
G M th M V d V d M t i l f Hi h T t E i i• G. Meetham, M. Van der Voorde, Materials for High Temperature Engineering Applications, Springer
• J. Betten, Creep Mechanics, Springer• Askeland: Materialwissenschaften, Spektrum Lehrbuch; 1994• Callister: Materials Science and Engineering - An Introduction, Wiley, New York, 1999• H. Schumann, Metallographie, Deutscher Verlag für Grundstoffindustrie, Leipzig• F. Vollertsen, S. Vogler, Werkstoffeigenschaften und Mikrostruktur, Hauser Verlag• P. Haasen, Physikalische Metallkunde, Springer-Verlag, Berlin• H -J Bargel G Schulze Werkstoffkunde VDI-Verlag DüsseldorfH. J. Bargel, G. Schulze, Werkstoffkunde, VDI Verlag, Düsseldorf• P. Sarrazin, A. Galerie, J. Fouletier, Mechanisms of High Temperature Corrosion, Trans
Tech Publications
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys3
lecture notes: http://www.metalle.uni-bayreuth.de then "Lehre" then "Vorlesungen", you will find the link to this lecture notes and three review talks we will do at the end.
What You Should Know:What You Should Know:
• basic thermodynamics• introduction to diffusionintroduction to diffusion• introduction to dislocations• phase diagrams• theory of elasticity• theory of elasticity• ...• basic materials science courses
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys4
Contents1 Introduction Basics
Contents1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Static)b) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys5
p ga) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
IntroductionIntroduction
• only alloys will be looked at (no ceramics no• only alloys will be looked at (no ceramics, no polymers).
• no coatings (BUT : practically all high temperature systems are coated!), simply not enough timeenough time.
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys6
Maximum Temperatures for li i f iff i lApplications of Different Materials
i i t tGroup maximum service temperature[°C] deformation/damage mechanism
Polymer up to 300 melting, decomposing (pyrolyze)
Glass up to 800 viscous flow
Fe-Basis (coated) up to 1100Fe-ODS up to 1300
Metals
Fe ODS up to 1300Ni-base up to 1200Pt-base up to 1600
refractory metals in inert h b 1600
creep, dislocation climb,grain boundary sliding
atmosphere above 1600MoSi2 up to 1800
Ceramics SiC up to 1600viscous flow, glass transition temperature grain boundaryCeramics SiC up to 1600 temperature, grain boundary
sliding
Composits (SiC/C) up to 1600 complex
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys7
p ( ) p p
Overview MaterialsOverview Materialsen
gth
usab
le st
ru
source: Plansee AGPlansee AG, Reutte, Tirol, Austria
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys8
temperature [°C]500 1500 2000
Taking Density into AccountTaking Density into Accounten
gth
usab
le st
ru
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys9
500 1500 2000temperature [°C]
Oxidation ResistanceOxidation Resistanceen
gth
usab
le st
ru
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys10
500 1500 2000temperature [°C]
Refractory Metals:
Most common definition ofwider definition Most common definition of
refractory metals (refractory = widerspenstig, halsstarrig):
of refractory metals
two elements of the 5. and three elements of the 6. period with melting points higher
Tm of platinum
with melting points higher than Pt. Processing in general by powder metallurgy.
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys11
DensityDensity
R PtOs, IrReWTa
Pt
Au
Os, Ir
Ru, Rh, PdHf
TcMo
PdMo
NbAg
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys12
Abundance of ElementsAbundance of Elements
to find 1 atom Rh within a bunch of Si-atoms is comparable toatoms is comparable to find one individual person within the word population
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys13
population
Material ChoiceMaterial Choice
• temperature• environment• moving/non-moving part• design complexity (how to manufacture)• price constrictions (depending on applicationprice constrictions (depending on application
of system). Reduction of 1 kg in weight:car 0 5 €– car ~ 0 - 5 €
– plane ~ 100 – 500 €
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys14
– aerospace ~ 100.000 - 500.000 €
Influence of onInfluence of ... on ...• temperature:temperature:
– phase transitions, volume fractions, ...– diffusion ( recrystallization, dislocation climb, diffusional creep, ... )– thermal fatigue (TF)
• mechanical:– creep– fatigue (low cycle, LCF, high cycle fatigue, HCF)
i t• environment:– oxidation– corrosion– corrosion
• combinations:– thermo-mechanical fatigue (TMF)
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys15
thermo mechanical fatigue (TMF)– stress corrosion cracking, stress oxidation, ...
BasicsBasicsThermodynamics ↔ KineticsThermodynamics ↔ Kinetics
Boltzmann-statistics: energy ofmovement increases with temperature 3p
Tk23u Batomkin ⋅=
TRQ
0 e ⋅−
⋅ε=ε &&Tk3Tk
232u2u BBatomkinatomtotal ⋅⋅=⋅⋅=⋅=
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys16
0Arrhenius-plotTR3U
moltotal ⋅⋅= 0,33 eV, bzw. 32 kJ/mol bei 1000°C
Vacancy ConcentrationVacancy Concentration
F U T S t ti iF = U - T·S non-zero vacancy concentration is in thermodynamic equilibrium
TRQ
v
vac
ec ⋅−
= Qvacnickel = 1,36 eV (energy necessary to create one vacancy)
T[°C] 20 300 450 800 1000 1200 1454
T/Tm 0.17 0.33 0.42 0.62 0.74 0.85 1.00
cv 10-23 3·10-12 10-9 10-6 10-5 7·10-5 3·10-4
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys17
equilibrium vacancy concentration for nickel
Nickel Vacancy ConcentrationNickel Vacancy Concentration
100
10 5
entra
tion 10-5
10-10
canc
y co
nc
10-15
Nickel Vacancy Concentration
vac
10-20
Nickel Vacancy Concentration
ncen
tratio
n [
10-4
]
1,00
temperature [°C]
0 200 400 600 800 1000 1200 1400 160010-25
Tm0 200 400 600 800 1000 1200 1400 1600
vaca
ncy
con
0,100,01
T
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys18
temperature [°C] Tm
DiffusionDiffusion
cDj ∇⋅−=rv
1. Fick's law[j] ( ) 2 1[j] = (atoms) · m-2 · s-1
[D] = m2 · s-1[D] m s
[c] = (atoms) · m-3
diff ivacancy diffusion or volume diffusion
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys19
Coefficient of DiffusionCoefficient of Diffusion
Qvac energy to create a vacancyQ i ti activation energy to migrate a vacancyQmigration activation energy to migrate a vacancyQSD activation energy for volume diffusion
QSD = Qvac + Qmigration
TkQ
0Tk
)QQ(
0
SDmigrationvac
eDeDD ⋅−
⋅
+−
⋅=⋅= 00
QSD ≈ 17 ·kB ·Tm QSDnickel ≈ 2.5 eV = 244 kJ/mol
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys20
(for a perfect crystal; defects will lower the activation energies)
Dependence Melting Point and Enthalpy of Vacancy Creation
T Q t lelement Tm[°C] 17·R·Tm
Qvac[eV]
crystal structure
Pb 327 0 88 0 57 fccPb 327 0.88 0.57 fcc
Al 660 1.36 0.68 fcc
Cu 1 085 1.99 1.29 fcc
Ag 1 235 2.21 1.12 fcc
Ni 1 455 2.53 1.78 fcc
Pt 1 768 2 98 1 32 fccPt 1 768 2.98 1.32 fcc
Mo 2 623 4.23 3.00 bcc
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys21
W 3 422 5.40 4.00 bcc
QSD versus TQSD versus Tm
400 kJ/mol
0 13 k /( l )0.137 kJ/(mol·K)≈ 17 · kB ·NA
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys22
Coefficient of DiffusionCoefficient of Diffusion
Steep slope indicates a p phigh activation energy.
S ll l t diffSmall elements diffuse faster.
Diffusion in fcc crystals slower than in bcc crystals.y
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys23
Coefficient of Diffusion with DefectsCoefficient of Diffusion with Defects
Coefficient of diffusion of Th i W
surface diffusion
in W.
Overall velocity for diffusion grain boundary diffusion
depending on grain boundary thickness, grain size and volume diffusion
dislocation density.pipediffusion
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys24
Pipe DiffusionPipe DiffusionD D + a ρ DDeff = DSD + adisl. · ρ · Ddisl.
adisl. area of dislocation core( ≈ 5 b2 ≈ 0 3 nm2)ol me diff sion ( ≈ 5 b2 ≈ 0.3 nm2)
ρ dislocation density
D i diff i l
volume diffusiondominant
pipe diffusiondominant Ddisl. pipe diffusion along
dislocation core
t fl D
dominant
increasing
atom flux ~ D·area
2grainSD dD~
timeatoms
⋅⎟⎠⎞
⎜⎝⎛
nbD~i
atoms 2disl ⋅⋅⎟
⎠⎞
⎜⎝⎛
decreasing
dashed line:
diffusion in crystal by the velocity of pipe diffusion
graintime ⎠⎝
22 bDnbDdD
identical atom fluxes if:time .disl
.disl⎟⎠
⎜⎝
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys25
ρ⋅⋅=⋅⋅=⋅ 2.disl
grain
2.dislgrainSD bD
dbDdD
Grain Boundary DiffusionGrain Boundary Diffusion
Deff = DSD + π · δ / d · Dgrain bound.
with:volume diffusiondominant
grain boundary diffusion
δ effective grain boundary thickness ( ≈ 2 b ≈ 0.5 nm)
dominantfinegrain
d grain size
D pipe diffusion along
coarsegrain
Ddisl. pipe diffusion along dislocation core
dashed line: diffusion in crystal by the velocity
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys26
y y yof grain boundary diffusion
Activation Energies Indicating Mechanism Changes
~ QSD
Single crystal aluminium, oriented such that <110>{111} slip is activated.
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys27
Lytton, Shepard and Dorn, Trans. AIME 212 (1958) 220
Diffusion in Ordered Structures ( lli h )(Intermetallic Phases)
• High binding energies high activation• High binding energies high activation energies low coefficient of diffusion
• For example NiAl: very low enthalpy of ordered B2 structure low enthalpy outweighs entropyB2 structure low enthalpy outweighs entropy
ordered up to meltingt ttemperatureTm
Ni = 1454°CTm
Al = 660°CTm
NiAl = 1638°C
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys28
m
Second Fick's LawSecond Fick s LawC b l d d di tl f fi t Fi k' l
cDtc
Δ⋅=∂∂
Can be concluded directly from first Fick's law.
Similar in heat transfer systems electricalt∂ Similar in heat transfer systems, electrical potential, ... .
1( )x1)x(f1 Γ−=
⎟⎞
⎜⎛Γ
x1)(f0.6
0.8
f1(x)
⎟⎠
⎞⎜⎝
⎛Γ−=5.0
1)x(f2
⎟⎞
⎜⎛Γ
x1)x(f0.2
0.4
f2(x)
f3(x)
⎟⎠
⎜⎝
Γ−=05.0
1)x(f3
( ) ⎟⎞
⎜⎛ xsolution to these
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys29
0.5 1 1.5 2( ) ⎟⎟⎠
⎞⎜⎜⎝
⎛Γ⋅−−=
tD2xccc)t,x(c 011
solution to these boundary conditions:
Thermal ConductivityThermal Conductivity
The most simple, stationary case: no heat radiation, constant temperatures in front and back of component.
λ … coefficient of heat (or thermal) conductivity: λ = a · cp · ρ
a … coefficient of temperature conductivity
cp … heat capacity
ρ … density
compare:
cDj ∇⋅−=rr
Tλq ∇⋅−=r
&r
c∂ T∂
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys30
cDtc
Δ⋅=∂∂ ΔTa
tT
⋅=∂∂
Temperature Distribution with h l i i ( )Thermal Barrrier Coating (TBC)
cooling aircooling air
hot air
Wärmedämm-schicht
Haftvermittlerschicht GrundwerkstoffTBC bond coat substrateschicht
In case of transients, the temperature should reach a stable distribution as fast as possible in order to reduce thermal stresses ( temperature conductrivity as high as possible).I f t ti i t h t d ti it l d t h t fl i t th lid
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys31
In case of stationary circumstances, heat conductivity leads to heat flow into the solid.
Material Parameters at RTMaterial Parameters at RT
heat cond heat cap density temp cond
⎥⎦⎤
⎢⎣⎡
⋅KmW
⎥⎦
⎤⎢⎣
⎡⋅KkgJ
⎥⎦⎤
⎢⎣⎡
3cmg
⎥⎦
⎤⎢⎣
⎡ −
sm10
26
material/property
heat cond.λ
heat cap.cp
densityρ
temp. cond.a
⎦⎣ g ⎦⎣ ⎦⎣
ferritic steel 45 460 7.8 13.0
austenite steel 15 500 8.0 3.8
Ni-base alloys 11 450 8.2 3.0
Mo 145 240 10.2 59.0
Ti alloys (α-rich) 7 530 4.5 2.9
Al 210 890 2.7 87.0
Al2O3 bei RT( Al2O3 bei 1000°C )
25( 6)
800 3.9 8.4source: Bürgel
Attention: Heat conductivity strongly depends on alloy composition see steels and pure
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys32
Attention: Heat conductivity strongly depends on alloy composition, see steels and pureNi with 91 W/(m⋅K) in comparison to Ni-base alloys with 11 W/(m⋅K)
ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys33
a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
Microstructure is NOT stableMicrostructure is NOT stable
annealed deformedannealed deformed
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys34
stress-relieved recrystallized
RecrystallizationRecrystallization
time dependence of recrystallization can berecrystallization can be approximated by Avrami Johnson MehlAvrami-Johnson-Mehl function:
n
0tt
e1f⎟⎠⎞⎜
⎝⎛−
−=r e1f
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys35
Grain CoarseningGrain Coarsening
• driving force: reduction of grain boundary energygy
• T > 0.7 · Tm
d f i• no pre-deformation necessary• self-similar systemse s sys e• Ostwald ripening d ~ t1/3 (big grains eat up
ll i )small grains)• new grains have low dislocation density
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys36
g y
Grain CoarseningGrain Coarsening
monomodal
bimodal (some grain boundaries are pinned, e.g. by precipitates)
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys37
Precipitate HardeningPrecipitate Hardening
Requirements:• solid solution at higher
t t ( bilit ttemperatures (ability to homogenization heat treatment)treatment)
• during cooling a two-phase region should be reachedg
• in general: cooling rate as high as possible, thereafter g pannealing (in the two-phase region) to let grow the
i i
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys38
precipitates
Thermodynamic ↔ KineticThermodynamic ↔ Kinetic
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys39
Example: Al-Cu AlloyExample: Al Cu Alloy
G i i P tGuinier-Preston Zones leading to θ-Precipitates (Al2Cu) have paved the way to the success of Al-alloys
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys40
Other Examples of i i h d iprecipitate hardening:
Al2Cu in AlCu alloy:
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys41
nickel-base superalloyplatinum-base superalloy
Time Dependence of Precipitation Hardening
nucleation growth coarseningnucleation, growth, coarsening
T = const.
dT precipitate size λT distance between precipitates
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys42
fT volume fraction of precipitates
Coherent - Semicoherent - IncoherentCoherent Semicoherent Incoherent
(mit Orientierungsbezug) (ohne Orientierungsbezug)
misfit ( ) aa
aaa
aaa
aaaa:
T
MT
M
MT
MT21
MT Δ≈
−≈
−≈
+−
=δ
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys43
( ) aaaaa TMMT2 +
Energy ConsiderationEnergy Consideration
ΔGtotal = ΔGvol + ΔGboundary + ΔGstrain + ΔGdefect
total change in free enthalpy
strain enthalpy (elastic energy + dislocation line energy)
enthalpy of phase boundary (scales with surface)
reduction of enthalpy by precipitation coupled with a defect
enthalpy of formation of matrix to precipitate (scales with volume)
py p y ( )
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys44
Heterogeneous NucleationHeterogeneous Nucleation
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys45
TEM-Micrograph of TiC Precipitates at Di l i i A i i S lDislocations in an Austenitic Steel
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys46
Ostwald-Ripening of PrecipitatesOstwald Ripening of Precipitates
d3 - d03 ~ D⋅t here for T/Tm ≈ 0.74
' ti l i i IN 738 LC tγ' particle size in IN 738 LC atT = 920°C.
particle coarsening constant of(50 nm)3/h(50 nm)3/h
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys47
ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys48
a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
Room Temperature (RT) versusHi h T (HT) D f iHigh Temperature (HT) Deformation
• most alloy properties at room temperature are time and rate independent (elastic constants, tension stress, ... ), tension stress experiment.
• For T > 0.4 · Tm the properties (deformation) will be time m p p ( )and rate dependent, creep experiment.
deformation hardening fine grain hardening solid solution strengthening
precipitate hardening
cold deformation (RT) strong medium medium to strong medium to strong
creep (HT)
temporary hardening, reduced creep rupture strength, may lead to
recrystallization
reduced strength with fine grain material coarse grain, ideally
single crystal
medium medium to strong
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys49
Change in Materials Properties with Temperature
Material properties of steel and Ni alloys at elevatedNi-alloys at elevated temperatures. Comparison b t h t t d lbetween short-term and long-term parameters.
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys50
Tension ↔ Creep ExperimentTension ↔ Creep Experiment
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys51
Elastic (E-)Modulus andi iPoisson's Ratio
)1(2EG
ν+⋅=shear modulus G
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys52
Anisotropy and Temperature Dependence of El i C i Ni b S llElastic Constants in Ni-base Superalloys
D. Siebörger, H. Knake, U. Glatzel, Mat. Sci. Eng. A298 (2001)
Orientation dependence of Young’s modulus E of matrixphase Distance from the center tophase. Distance from the center to the surface indicates the magnitude of the Young’s modulus i thi di ti
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys53
in this direction.
High Temperature DeformationHigh Temperature Deformation
• dislocation glide (Peierls stress, in fcc and hcp very small and for T > 0.15 Tm negligible)
li f di l ti d di l ti i t ti (f l• cross slip of screw dislocations and dislocation interactions (for a low stacking fault energy larger dislocation spacing thermal activation necessary T > 0 2 T influence on deformation rate)activation necessary, T > 0.2 Tm, influence on deformation rate)
• climb of edge dislocations to overcome obstacles:diffusion at completepdislocation line
T > 0.4 Tm
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys54
Dislocation ClimbDislocation Climb
climb of edge dislocations to annihilate each other.
arrangement in low energy configurations (sub-grain boundaries), climbing around b l (l i h lidabstacles (leaving the glide
plane)
movement of screw dislocations ith kink
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys55
dislocations with kink
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys56
Internal Back StressInternal Back Stress
i l i li b ll ihil i f di l iDislocations climb allows annihilation of dislocations and to establish a constant dislocation density, resulting in an internal back stress of:
bG ρασ ⋅⋅⋅= bG.int
1bG 1σdislocation = and
r1
2bG⋅
π⋅⋅
r1
=ρ
G shear modulus, α constant 0.3 - 1, b magnitude of Burgers vector
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys57
Creep ExperimentCreep Experiment
behavior of pure metals:
primary secondary tertiary:
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys58
primary secondary tertiary:
Creep Experimental Setup up to 1400°C
Constant temperature and stress or a d st ess oload
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys59
Creep Experimental Setup forElectrical Conductivity Materialy
up to Melting Temperature
Pyrometer from left, optical strain measurement from right, both contact-free.
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys60
g ,
Interrupted creep testsInterrupted creep tests
[001] orientation 1123K 650MPa67
single crystal (SX) nickel base superalloy (habilitation thesis Glatzel)8x10-6
[001] orientation, 1123K, 650MPa
stra
in [
%]
3456
[001] orientation, 1123K, 650MPa
in ra
te [
1/s]
4x10-6
6x10-6
0 10 20 30 40 50 60 70
s
012
0 10 20 30 40 50 60 70
stra
i
0
2x10-6
time [h]
0 10 20 30 40 50 60 70
time [h]
0 10 20 30 40 50 60 70
1123K, 650 MPa]
10-5
logarithm of strain rate versus strain,
stra
in ra
te [
1/s]
10-6
logarithm of strain rate versus strain (most valuable information for
i l i i )
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys61strain [%]
0 1 2 3 4 5 610-7
materials scientist)
Different Creep StagesDifferent Creep Stages
• primary creep: strain rate dε/dt decreases material hardens
• secondary creep stage: strain rate constant hardening and softening are in equilibriumhardening and softening are in equilibrium dislocation multiplication and annihilation in equilibrium disl. density ρ = const.
• tertiary creep: necking (creep pores) developtertiary creep: necking (creep pores) develop local stress and strain rate increases
drasticallyUniversity Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys62
drastically.
Modelling of Primary and dSecondary Creep Stage
l idensity velocity
vb= ρε& vb ⋅⋅= ρε
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys63
Problem with Low Creep RatesProblem with Low Creep Rates
Life time of stationary gas turbines > 20 years Assuming aLife time of stationary gas turbines > 20 years. Assuming a maximum deformation of 3%, this leads to an assumed
d i ( l i i d isteady state strain rate (neglecting primary and tertiary creep) of about = 5·10-11 s-1. Reliable data in labs statesteadyε&can only be obtained down to 1·10-9 s-1 (1 μm change with l0 = 25 mm after 10 h one creep experiment with 3.5%l0 25 mm after 10 h one creep experiment with 3.5% strain per year!).Th f ithi i it l b t dTherefore within university labs we are two and more orders of magnitude too fast than real life in a stationary
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys64
gas turbine!
Engineering Creep CurvesEngineering Creep Curves
raw data creep curves:raw data creep curves:
time to failure: time - strain
isochrone time to failure: isochrone strain
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Natural Creep LawNatural Creep Law
b& vbstatesteady ⋅⋅ρ=ε&
2external
bG⎟⎠⎞
⎜⎝⎛
⋅σ
≈ρbG ⎠⎝ ⋅
1v σexternal~v σ
natural creep lawbG
~ 2
3external
⋅σ
ε&
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bG
Norton Creep Law (Empirical)Norton Creep Law (Empirical)
TRQ
nexternal
creep
eA ⋅
−
⋅σ⋅=ε&with the Norton creep exponent "n" and
Qcreep ≈ Qself diffusionQcreep Qself diffusion
l b kpower law break down (plb) stress dependence
of the stationary T = const.
dislocation
creep rate of the austenitic steel 800 H at 900°C and
climbH at 900°C and 1000°C:
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diffusional creep
Diffusional CreepDiffusional Creep
• Nabarro-Hering creep (pure volume diffusion)
D ΩTkh
D2 2
diffusionselfNH ⋅
Ω⋅σ=ε&
• Coble creep (grain boundary diff.)
TkhD
2 3boundarygrain
C ⋅Ω⋅σ⋅δ
=ε&
h grain size, δ thickness of grain boundary
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Combined NH and Coble Creep:Combined NH and Coble Creep:
2eff
3boundarygrain
2diffusionself
CNHdiff iD~
DD2 ⋅
Ωσ⎟⎟⎞
⎜⎜⎛ ⋅δ⋅π
+⋅Ω⋅σ
⋅=ε+ε=ε &&&232CNHcreepdiffusion hTkhhTk
2 ⎟⎟⎠
⎜⎜⎝
+⋅
ε+εε
hD
DD boundarygraindiffusionselfeff
⋅δ⋅π+=
real geometry (non-cuboidal grains)
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Temperature Dependence of iStationary Creep Rate
σ = 28 MPA = const.
fcc alloys:
TRQcn
53A−
⎟⎞
⎜⎛ σ& TR5,3
SFs eE
A ⋅⋅⎟⎠⎞
⎜⎝⎛ σ⋅γ⋅=ε&
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Austenitischer Stahl 800H
Activation Energy for CreepActivation Energy for Creep
slope = 1
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Constant Load ↔ Constant StressConstant Load ↔ Constant Stress
( )nn )1(FF ⎟⎞
⎜⎛ ε+⋅⎞⎛ ( )nn
000
00n
0 1A
)1(FAF
ε+⋅σ⋅ε=⎟⎟⎠
⎞⎜⎜⎝
⎛ ε+⋅⋅ε=⎟
⎠⎞
⎜⎝⎛⋅ε=σ⋅ε=ε &&&&&
failure
in case the gauge length deforms uniform with constant volume
This method is applicable to determine the stress exponent "n" only, if the secondary creep state y, y plasts to at least 10%
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ln = ln + n · ln σ0 + n · ln (1+ε) = const. + n · ln (1+ε)ε& 0ε&
Ashby Deformation Mechanism Maps
n = 3
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Ashby Deformation Mechanism Maps
Versetzungsklettern !dislocation climb !
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Deformation Mechanisms:Deformation Mechanisms:
Elastic Deformation: Spontaneous and reversible deformation. In the elastic region: σ = E·ε (rule of thumb: εe, max ≈10-3, but definitely << 1%). Plastic or non-reversible deformation achieves way higher strains. Coble-creep (grain boundary diffusion) is in theory possible even at 0 K.p (g y ) y p
Dislocation Glide: … without significant time dependent recovery (climb). Is dominant in the complete temperature regime from 0 K up to the melting point Tm at moderate and higher stress levels. At low temperatures (< 0 4 T ) dislocation glide has the lower boundary in the range of the elastic stress limittemperatures (< 0.4⋅Tm) dislocation glide has the lower boundary in the range of the elastic stress limit (typically 10-3⋅E).
Dislocation Climb: At higher temperatures (> 0.4⋅Tm) and lower stress levels dislocation climb plays the major role => time dependent constant strain rate (dε/dt)ss ~ σn, with a Norton stress exponent in-between 3 und 8.
Diffusional Creep: In-between 0 K und 0.8⋅T and very low stress levels: Coble-creep (grain boundaryDiffusional Creep: In between 0 K und 0.8 Tm and very low stress levels: Coble creep (grain boundary diffusion). Below 0.4⋅Tm not measurable. For geological times a time dependent deformation can be determined. Transition to Nabarro-Herring creep (volume diffusion) is dependent on grain size and grain boundary thickness The transition temperature from coble to Nabarro Herring creep can be explained by
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys75
boundary thickness. The transition temperature from coble to Nabarro-Herring creep can be explained by the different activation energies of volume and grain boundary diffusion.
Creep of AlloysCreep of Alloys
a) interaction dislocationand impurity (low temp.)
solutionsolidi bG σ+ρ⋅⋅⋅α=σ
b) stationary dislocationpinned by impurities(C ll l d )(Cottrell clouds)
c) pulled off Cortrell clouds(Lüd b d )(Lüders bands)
d) gliding dislocation trailsi iti b hi d ( i lid )impurities behind (viscous glide)
e) impurities faster than dislocation (very high temp., no hardening)
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f) annihilation due to dislocation climb
Precipitation HardeningPrecipitation Hardening
eprecipitatsolutionsolidi bG σ+σ+ρ⋅⋅⋅α=σ
threshold stress concept (with n ≈ 3 - 4 and Qcreep = Qself diffusion):
TRQcn
0ss e
EA ⋅
−
⋅⎟⎠⎞
⎜⎝⎛ σ−σ⋅=ε&
mechanism temperaturecoherent and semi-
coherent phase boundaries
in-coherent phase boundaries
cutting 0 K up to Ts yes no
bypass by Orowan 0 K up to Ts yes yes
li b b l 0 4 T
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climb over obstacles > 0.4⋅Ts yes no
Hardening Mechanisms as Function of Precipitate Size
dT0 initial precipitate sizedT0 initial precipitate size
σ1 and σ2 arbitrary external stress levels
passing by:
li bi
Td~ε&
1&
= cutting
climbing:
Cutting is relevant only for coherent
2Td
~ε
precipitates
Dependence of stationary creep rate on initial precipitate size for two different
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p pexternal stress levels
Pinning of Dislocations by bid i i i lCarbides in Austenitic Steel
T 1000°C 25 MP bid f th t TiC d M C
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T = 1000°C, σ = 25 MPa, carbides of the type TiC und M23C6
Very High Volume FractionsVery High Volume Fractions
Volume fractions of 70% are only achievable with non spherical precipitatesVolume fractions of 70% are only achievable with non-spherical precipitates. Spacing between precipitates is getting smaller Orowan stressσO ≈ G·b/L necessary. For small strains precipitates are not cut byσOrowan G b/L necessary. For small strains precipitates are not cut by dislocations. With G = 90 GPa, b = 0.25 nm, L ≈ 75 nm => σOrowan ≈ 300 MPa
nickel base superalloys
ODS llODS alloys:
σOrowan ≈ .vol
dfbG ⋅⋅
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.partd
Dispersion Hardening(oxide dispersion strengthened alloys (ODS-alloys))
precipitate strengthenedyield precipitate strengthened
dispersion strengthened
stress
temperature
back-side pinning of dislocation by
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p g yODS-particle (Rössler + Arzt)
Summary:d i h iHardening Mechanisms
Internal back stress in steady state regime: ρασ ⋅⋅⋅= bGi
Orowan stress in case of precipitates or particles: σOrowan ≈ G·b/L
Solid solution strengthening: ΩΔΩ⋅≈ .constsolutionsolidσ
ΔIn case of coherent precipitates: E
aa
coherencyΔ
≈σ
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Creep DamageCreep Damage
creation of a creep pore in poly-crystalline material due to disloction glide:
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a) cracks at grain boundaries b) cavities (micropores) at grain boundaries
Creep DamageCreep Damage
nucleation, not detectable with OMfracture
micropore, difficult to detectmicro cracks
pear necklace like chain of micropores (easy detectable)
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Extrapolation of Time-to-Fracture Data(L Mill l L Mill )(Larson-Miller plot, Larson-Miller parameter)
M k G t l ti ith t t K d t 1
Kt =
Monkmann-Grant relation with constant K and exponent m ≈ 1:
or: ( )lnmK)tln( ε&mss
ftε
=&
or: ( )ssf lnmK)tln( ε⋅−=
TRQcreep
eB ⋅−
⋅=ε& or: 1BB)ln( 21ss ⋅−=ε&ss eBε T
)( 21ss
11T1PC
T1BmBmK)tln( 21f ⋅+−=⋅⋅−⋅−=
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with material dependent constants C and P
Larson-Miller-PlotLarson Miller Plott ti t bi b t 20 f i 130 000 hstationary gas turbine, about 20 years of service ~ 130.000 h
Comparison of CMSX-6, LEK 94 d CMSX 4LEK 94 and CMSX-4, patent Wöllmer, Glatzel,
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P = T⋅[20 + ln(tf)]⋅10-3 (T in K, tf in h)Mack, Wortmann
Comparison LEK 94 withdCMSX-4 and CMSX-6
3
500CMSX-6 [Wortmann 88] 8.0 g/cm3
CMSX-4 [Erickson 94] 8.7 g/cm3
CMSX-4 [Frasier 90] 8.7 g/cm3
LEK-2 8.5 g/cm3
MPa
]
gLEK-4 8.2 g/cm3
LEK-5 8.2 g/cm3
LEK-3 8.1 g/cm3
LEK-6 8 3 g/cm3
24 K
stre
ss [M 230
LEK 6 8.3 g/cmLEK-1C 8.4 g/cm3
LEK-1B 8.3 g/cm3
LEK-1A 8.2 g/cm3ΔT = 10 K
120
29 K
Not corrected
Larsen-Miller-parameter25 26 27 28 29 30 31 32
10 K
regarding density!
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Larsen Miller parameterP = T (20+log tB) 10-3
ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys88
a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
Time Dependent Variation of Stress d/ T d/and/or Temperature and/or ...
Wöhl di f T < 0 4 T Z ti f ti li it D dWöhler diagram for T < 0.4·Tm. Z time fatigue limit, D endurance fatigue limit
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a) type I metal (bcc) b) type II metal (fcc) endurance limit at 2·107
Change in Wöhler Diagram with d ldi iTemperature and Holding Time
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Thermal FatigueThermal Fatigue
Thermal breathing of turbine blade:a) heating phase: edges reach high temperatures faster than interior
b) cooling phase: edges cool faster than interior
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c) repeated thermal cycles lead to thermal fatigue cracks at edges
Thermal Strains and Stresses :Thermal Strains and Stresses :
εthermal = αthermal · ΔT, or: σthermal = E · εthermal
E ΔTσthermal = E · αthermal · ΔT
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Lower E-Modulus is Helpful:Lower E Modulus is Helpful:
orientation of single crystals in <100> direction reduces thermal stresses
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orientation of single crystals in <100> direction reduces thermal stresses
TMF and many other Time Dependent Test Techniques
Can not be covered in this lecture!
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ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys95
a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
High Temperature CorrosionHigh Temperature Corrosion
• oxidation: external and internal, passivation• carburization (internal carbides)carburization (internal carbides)• nitration: internal, seldom nitrite passivation• sulfurization: external (sometimes
passivation), seldom internalp ss v o ), se do e
Worldwide 1 ton iron per minute corrodes to rust (low temperature aqueous corrosion)
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temperature aqueous corrosion).
Ellingham-Richardson-DiagramEllingham Richardson Diagram
right hand and lower axesO2 partial pressure at T = 0.
As an example pO2ofO2
10-15 Pa = 10-20 bar = 10-17 mbar
is shown as a dashed line.is shown as a dashed line.
only the oxides below this lineonly the oxides below this line are thermodynamic stable.
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Time Dependent OxidationTime Dependent Oxidation
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Oxidation MechanismsOxidation Mechanisms
• logarithmic (not shown) low temperature oxidation which eventually comes to a stop or no measurable increase in oxide scale thickness (e.g. Al, Cr, Mg).
• parabolic mass change (Δm/A)2 ~ t. Diffusion through p g ( ) goxidation layer (either oxygen or metal). Most favorable oxidation behavior.
• linear mass change: oxide layer with cracks continuous contact with metal (e.g. Ta, Nb).contact with metal (e.g. Ta, Nb).
• mass loss: volatile oxides catastrophic oxidation (e.g. V, Mo W Cr Pt) You can see it inside a broken light bulb
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Mo, W, Cr, Pt). You can see it inside a broken light bulb.
Pilling-Bedworth RatioPilling Bedworth Ratio
PB = (volume of oxide of one metal atom)/(volume of metal atom)
Oxide TiO MgO Al2O3 MgO2 Ti2O3 ZrO2 Ti3O5 NiO FeO TiO2 CoO
PB 0.70 0.81 1.28 1.34 1.50 1.56 1.65 1.65 1.70 1.73 1.86
Oxide Cr2O3 FeCr2O4 Fe3O4 Fe2O3 SiO2 Ta2O5 Nb2O5 W
PB 2.05 2.10 2.11 2.15 2.15 2.50 2.68 3.40
ideal is 1.1 to 1.3
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Of course thermal expansion coefficients also play a major role for the stability of oxide scales.
Alloying Effects:Alloying Effects:
different elements have different oxygen affinitydifferent oxygen affinity
concentration changesconcentration changes
diffusion rates are different
oxide layer contains other ymetals
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Example Ni-Cr-AlExample Ni Cr Al
Ni Cr 10 Al 5oxide layer and yinternal oxidation occurs
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Observations for the [MB1]noch andere Eigenschaften reinschreiben?
Superalloy Rene N5
Diploma thesis Bensch, 2009and submitted paper
layer number layer composition properties
1 cover oxide layer NiO, CoO thick and porous monophase layer
2 interlayer of oxides NiAl2O4 , NiTa2O6, Cr2O3 thick and porous layer consisting of two fractions
3 third oxide layer Al2O3 dense and thin monophase layer
4 γ’-free layer see Tab. 1 Al-content of 2.2 wt. %
5 γ’ reduced layer composition in between layer number 4 and 6 reduced Al content γ’ morphology change
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5 γ reduced layer composition in-between layer number 4 and 6 reduced Al content, γ morphology change
6 two-phase centre region nominal composition of René N5 (Tab. 1) regular γ’/ γ structure, see Fig. 6 f)
ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
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a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
High Temperature AlloysHigh Temperature Alloys
T > 500°C, Application in:• energy generationenergy generation• engines (cars, trains, airplanes, ships, ... )• chemical industry• metallurgy• metallurgy• mechanical engineering
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Overview MetalsOverview Metalsele struc T T ρ max O solubility advantages/disadvantageselem.
struc-ture
Ttrans.Tm[°C]
ρ[g/cm3]
max. O-solubility[at.%]
advantages/disadvantages
Ti αhdpβ k
8821855
4.54.5
31.98
+ low density+ high melting point+ b d t il blβ krz + abundant available+ low αth. (~ 10-5 K-1)− now alloy known with adequate strength for temperatures > 600°C− high oxygen and nitrogen solubility > 700°C, increased brittleness− linear oxidation > 800°C− low thermal conductivity− ignition hazard
V krz 1910 6.1 17 − catastrophic oxidation; Tm(V2O5) = 658°C
Cr krz 1863 7.2 0.0053 − very brittle at RT; conventionally not processableCr krz 1863 7.2 0.0053 very brittle at RT; conventionally not processable
Mo krz 2623 10.2 0.03 + very high creep strength+ lowαth, high thermal conductivity, good thermal fatigue strength− very brittle at RT− catastrophic oxidation; Tm(MoO5) = 795°Cp m( 5)− no long lasting coating available
W krz 3422 19.3 ≈ 0 + highest melting point of metals (only C with even higher Tm)+ very high creep strength+ low αth, high thermal conductivity, good thermal fatigue strength
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− very brittle at RT− catastrophic oxidation > 1000°C durch hohe WO3-Abdampfrate− no long lasting coating available− very high density
Overview MetalsOverview Metals
elem. structure Ttrans.Tm
[°C]
ρ[g/cm3]
max. O-solubility
[at.%]
advantages/disadvantages
α krz 912 7.9 0.0008 + very good corrosion resistance by alloying with Cr or (Cr + Al)
Feγ kfzδ krz
13951538
7.77.4
0.00980.029
y g y y g ( )+ γ-structure can be stabilized down to RT (by Ni)+ very good processable and weldable+ low cost (~ 1 €/kg)− strength at high temperatures (> 700°C) limited
Co ε hdpα kfz
4221495
8.88.7
≈ 00.048
+ very good corrosion resistance by alloying with Cr or (Cr + Al)+ Co-alloys castable in air good weldability− only moderate hardening available − Ni-additions necessary to stabilize fcc structure, reduces strength
i kf 14 8 9 0 0 b d ibili i f ll i hi h h i iblNi kfz 1455 8.9 0.05 + broad possibilities for alloying, high strength increase possible+ very good corrosion resistance by alloying with Cr or (Cr + Al)+ processable − relatively low melting point−αth high, low thermal conductivityth. g , y
Pt kfz 1772 21.5 ≈ 0 + high corrosion and oxidation resistance+ high melting point− very high density− very expensive (~ 33 €/g)
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Evolution of materialsused in aero-engines
The earlier approach of technolog transfer from militar to ci il isThe earlier approach of technology transfer from military to civil is tending to switch direction.
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© www.azom.com
10 000 h Life Time10.000 h Life Time
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Example of Intermetallic Phases (Ni-Al-System)
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Ni-Al Intermetallic PhasesNi Al Intermetallic Phasesphase structure T ρ advantages/disdavantagesphase structure Ttrans.
Tm[°C]
ρ[g/cm3]
advantages/disdavantages
Ni3Al L12 1383 7.5 + anomalous temperature dependence of strengthb h Ni i (f )+ same structure base than Ni matrix (fcc)
+ stable for larger Al variations > 1 wt.% Al+ ductile as single crystal− high density
b ittl l t l ( b hi d d b b d i ( i− brittle as polycrystal (can be hindered by boron doping (grain boundary strengthener)−Al-content not sufficient to build stable Al2O3-layer reduced high temperature oxidation resistance
NiAl L10 1638 5.85 + very good oxidation resistance, since 30 wt.% Al+ high melting point+ low density+ ordered structure up to melting pointp g p+ high thermal conductivity+ low coefficient of thermal expansion− extremely brittle at temperatures below 500°C (von Mises criterion not fulfilled)
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)− low strength at high temperatures
NiAl, B2 Ordered Intermetallic Phase
• At a first sight very interesting (see advantages) but despite many efforts and many g ) p y y100 Mio. US$ research money spent, up today no bulk usage of NiAl has been achievedno bulk usage of NiAl has been achieved.
• BUT: aluminum coatings leading to NiAl layers is heavily used.layers is heavily used.
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ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
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a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys
MTS-Factory in BayreuthMTS Factory in Bayreuth
ground-breaking ceremony: 20.02.2008, topping-out ceremony: 06.06.2008
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g g y , pp g ystart of production: ~ 12/2008
MTS-Factory June 2008MTS Factory, June 2008
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MTS-Factory June 2008MTS Factory, June 2008
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys116
MTS-Factory June 2008MTS Factory, June 2008
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Processing of a Turbine l dBlade
FPIX-Rayy
F i W h h l f h l i i
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Feinguss, Wachsausschmelzverfahren, lost wax investment casting, ...
Archaeological Evidence (Bibracte) ~ 50 B.C.
ceramic mould filled with wax
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cloth clip
Singly Crystal Castin in Bayreuth h h i f l d llat the Chair for Metals And Alloys
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ContentsContents1 Introduction Basics1. Introduction, Basics2. Stability of Microstructure3. Mechanical Properties
a) Staticb) Cyclic (Fatigue)
4 High Temperature Corrosion4. High Temperature Corrosion5. High Temperature Alloys6. Lost Wax Investment Casting7. Depending on Time: Lectures on
University Bayreuth, Advanced High Temperature Alloys Uwe Glatzel, Metals and Alloys121
a) SX Ni-Base Superalloys b) LEK 94 c) Pt-Base Superalloys