Co Based Alloys
Co Based Alloys
Co Based Alloys
Cobalt
History
1930s
Co-Cr-Mo alloy Vitallium developed for dental prosthetics.
1940
1940s
s
HS-21 (derived from Vitallium) becomes important for
turbochargers and gas turbine applications.
Wrought Co-Ni-Cr
Co Ni Cr alloy S-816
S 816 used for gas turbine blades and
vanes.
Co-Ni-Cr-W alloy X-40 developed in 1943. Still used in gas
turbine vanes.
1950-1970
1950 1970
Ni-based superalloys strengthened by developed. Rapidly
surpassed capabilities of Co alloys. Co-based alloys lack
comparable precipitation hardening mechanism (doesnt
( doesn t this
sound similar to Mg alloys?)
2000s
Discovery of something new and exciting!
Ni
10.5
2
10
10
22
Cr
29.5
28
20
21.5
23.4
22
Al
Ti
0.25
Mo
5.5
W
7
15
10
7
14.5
Ta
9
3.5
B
0.012
0.005
*maximumamount
PredominantlycomposedofCo,Ni,Cr,W
Zr
0.015
0.35
C
0.25
0.3
0.1
0.85
0.6
0.1
Other
2 Fe
3 Fe*
0 90La
0.90La
General Characteristics
Austenitic matrix (FCC crystal structure)
20 30% Cr is added to provide oxidation and hot
corrosion resistance. This is the most important
addition.
dditi
C
Cr also
l provides
id some solid
lid solution
l ti strengthening
t
th i and
d
is of vital importance in precipitation strengthening.
Additional solid solution strengthening is provided via
additions of Ta,, W,, Nb,, Mo.
Physical Properties of Co
HCP when T<421C
FCC when T>421C
Co is also ferromagnetic
Tmp is 50C greater than Ni
AlloyingElement
ChangeinMeltingTemperature(F)
Raise
Tungsten
+1
Lower
Nitrogen
Iron
Chromium
Molybdenum
Vanadium
15
Manganese
15
Aluminum
20
Tantalum
30
Zirconium
30
Sulfur
40
Titanium
65
Niobium
70
Silicon
75
75
Boron
115
Carbon
120
Phase Equilibria
BCC
FCC
HCP
A.M.Beltran;CobaltBaseAlloys;inSuperalloysII,C.T.Sims,N.S.Stoloff,
A
M B l
C b l B
All
i S
ll
II C T Si
N S S l ff
andW.C.Hagel,editors;(JohnWiley&sons,NewYork,1987)p.139.
Predel,B.: CoCr(CobaltChromium).Madelung,O.(ed.).SpringerMaterials
TheLandoltBrnstein Database(http://www.springermaterials.com).DOI:
10 1007/10086082 907
10.1007/10086082_907
MostalloysarepredominantlycomposedofCo+Cr,Ni,and/orW
Chromium
Tungsten
g
Ti,Zr,Nb,
, , , Ta C
Principal
function
Austenite
stabilizer
Surface
stability+
carbide
former
Solidsolution
strength
MCformers
Carbide
formation
Problems
Lowers
corrosion
resistance
FormsTCP
phases
FormsTCP
phases
Harmssurface
stability
Decreases
ductility
X40
10
25
7.5
0.45
MM509
MM
509
10
24
70
7.0
3.5Ta,0.5Zr,
3
5 Ta 0 5 Zr
0.2Ti
0 60
0.60
L605
10
20
15.0
0.10
HS188
22
22
14.0
0.08
whenaddedin
excess
Examples
Small amounts of Aluminum (~ 5 wt.%) has been added to improve oxidation and hot corrosion
resistance. Used extensively in coatings.
Additions of Titanium,
Titanium have been shown to form a phase,
phase (Co
(Co,Ni)
Ni)3Ti.
Ti but to also stabilize undesirable
HCP-Co3Ti or Co2Ti-Laves phases).
Rare earth additions (0.08-0.15 wt.%) increases oxide scale adhesion and reduces oxidation
kinetics(RE effect).
Phase Equilibria
BCC
FCC
HCP
Predel,B.: CoCr(CobaltChromium).Madelung,O.(ed.).SpringerMaterials
TheLandoltBrnstein Database(http://www.springermaterials.com).DOI:
10.1007/10086082_907
A.M.Beltran;CobaltBaseAlloys;inSuperalloysII,C.T.Sims,N.S.Stoloff,
A
M B l
C b l B
All
i S
ll
II C T Si
N S S l ff
andW.C.Hagel,editors;(JohnWiley&sons,NewYork,1987)p.141.
AlloyingadditionsselectedtostabilizeFCCorHCPphases
oy g add o s se ec ed o s ab e
o
p ases
Rememberourdiscussionofalloydesign.
FCC/HCPtransition PossibilityofStackingFaults
Alloying
A.M.Beltran;CobaltBaseAlloys;inSuperalloysII,C.T.Sims,N.S.Stoloff,andW.C.Hagel,editors;(JohnWiley&sons,NewYork,1987)p.142.
Dislocationinteractionw/faultsproducesstrengthening.
Faultsarealsopreferentialnucleationsitesforcarbides;candegradeproperties.
Faults are also preferential nucleation sites for carbides; can degrade properties.
FCCstabilizingadditions(e.g.,Ni)areaddedtoinhibitSFformation&carbide
formationduringHTexposure.
0.02-0.20 wt.%
0.05-0.20 wt.%
0.25-1.0 wt.%
Solubilitylimitsat1260C
A.M.Beltran;CobaltBaseAlloys;in
SuperalloysII,C.T.Sims,N.S.Stoloff,andW.C.
Hagel,editors;(JohnWiley&sons,NewYork,
1987) 144
1987)p.144.
A.M.Beltran;CobaltBaseAlloys;in
SuperalloysII,C.T.Sims,N.S.Stoloff,andW.C.
Hagel,editors;(JohnWiley&sons,NewYork,
1987)p.145.
Carbide
CarbideformerscomefromgroupstotheleftofCointheperiodictable
formers come from groups to the left of Co in the periodic table
(Goldschmidtscriteria).Theseelementsaremoreelectronegativeandthus
morereactivethanCo.
Classes of Carbides
M3C2, M7C3, and M23C6 Carbides.
These are basically chromium carbides containing Co
Co, W
W, or Mo
in place of Cr.
M3C2 has a rhombic crystal structure and forms via a peritectic
reaction with Cr. It has been observed in some of the early
superalloys with low Cr contents.
M7C3 has a trigonal crystal structure and forms at low Cr/C
ratios. It can be dissolved during solution treating and in some
cases transforms to M23C6 during aging
aging.
Classes of Carbides
M3C2, M7C3, and M23C6 Carbides.
M23C6 generates very potent precipitation strengthening
strengthening. It is the
result from decomposition of the M7C3 carbides via reactions of
the form:
23C 7 C3 7C
23Cr
7Cr23C6 27C
6C+23Cr Cr23C6
decomposition
Reprecipitation
Classes of Carbides
M3C2, M7C3, and M23C6 Carbides.
Tend to form via a eutectic type reaction:
In
I castt alloys
ll
M23C6 comes outt interdendritically.
i t d d iti ll
Specific carbide morphology depends upon cooling rate.
Cast alloys:
Interdendritic
M23C6
Classes of Carbides
M6C and MC Carbides
These carbides are rich in refractory elements. They are used to
strengthen wrought and investment cast Co
Co-base
base alloys.
MC carbides are typically of the form: TaC, HfC, NbC, etc.,
Similar to Ni-base alloy systems, M6C carbides are generally
found in low-Cr alloys with Mo and/or W levels > 46 at.%.
M6C carbides are typically of the form:
M 3 M3C or M 4 M3C
(Co 0.45Cr0.3Ta 0.15 W0.1 )C
Classes of Carbides
M6C and MC Carbides
M6C carbides often form during
g service via a decomposition
p
reaction:
MC + austenite M 6 C
Example:
Blockycarbidestend todevelop
whenN2 ispresent.
Other phases
We stated that it was possible to form , just not the same as
a Ni-base superalloy.
In
I these
h
alloys
ll
= (Co,Ni)
(C Ni)3Ti.
Ti
However, the phase is unstable
above 760C.
Also, once you add Cr, it no
longer forms.
Mechanical Working
We want to break down the coarse carbides that
form during
g solidification. This can be done by
y
mechanical working.
FiguretakenfromCo:
CobaltinSuperalloys,The
CobaltDevelopment
Institute:1985;page10
Canworkwithcertaindrawbacks.
ItisalsopossibletoformTCPphases(,,
Laves).
Laves)
Stepsmustbetakentoavoidthem.Theyare
undesirableastheyaresitesfortheinitiation
d
bl
h
f h
offracture.
Carbidesstrengthenthesealloys,butarealso
potentialsitesforfractureinitiation.
Something New!
Co-based - Alloys
Based on ternary Co-Al-W
Co Al W
Off
Offer potential
t ti l for
f superalloy
ll type
t
performance
f
at higher temperature.