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Introduction
Welding is an integral part of most
modern construction and manufacturing
operations. On any given project, welding
operations frequently involve a range of
welding consumables and processes. It is
often necessary to repair flaws that form as
a result of service or defects created durM. A. QUINTANA is with The Lincoln Electric
Company, Cleveland, Ohio. M. Q. JOHNSON
is with Edison Welding Institute, Columbus,
Ohio. Paper presented at the AWS Annual
Meeting, April 1317, 1997, Los angeles,
Calif.
KEY WORDS
Carbon-Manganese Weld
Metal
Charpy V-Notch
Dilution
Electrodes
FCAW
Multipass Welds
Primary Metal
Retransformed Metal
SMAW
mized without considering dilution effects from either the underlying base
metal or a weld metal of different chemical composition. Welding consumable
specifications standardize on the type of
base material to be used for certification
and conformance testing. Accordingly,
electrodes are designed to produce weld
metal mechanical properties through optimization of the alloy design and the use
of slag/metal reactions to create the
proper composition and microstructure.
Depending on the anticipated service requirements and the operating characteristics desired, the alloy levels and slag
systems are optimized in different ways.
The introduction of elements through dilution/intermixing at levels not originally
intended can alter the weld metal properties and resulting weld performance.
For example, when welding high carbon
or microalloyed base metal, high concentrations of carbon or microalloying
elements in the weld metal can occur
through dilution. Similar dilution effects
occur when one welding consumable is
deposited over another of significantly
different composition. Further dilution
may also result in a loss of alloy elements
in the weld, if the base material or underlying weld metal possesses a leaner
composition than the welding consumable used to fabricate the balance of the
weld joint. In either case, a shift in chemical composition away from optimum
can occur.
The effect of such unexpected variations in chemical composition can be
undesirable changes in the mechanical
properties of the weld metal. While a
great deal of study has been devoted to
dilution effects from base metals, only
limited study has been conducted on the
effects of intermixing weld metals deposited by different processes/electrode
types. Most arc welding processes rely on
a protective slag and/or a shielding gas to
protect the weld metal from the atmosphere during welding. In this respect,
the FCAW-S process is unique. FCAW-S
consumables produce very little shielding gas and rely on the addition of large
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amounts of deoxidizers (primarily aluminum) to react with oxygen and nitrogen from the atmosphere during metal
transfer. FCAW-S welds typically contain
between 0.8 and 1.6 wt-% aluminum.
Since aluminum is a strong ferrite former,
it can be balanced with the addition of an
austenite stabilizer such as carbon, manganese or nickel to avoid primary solidification and stabilization of -ferrite at
high temperatures. As a result, many
FCAW-S weld deposits can contain substantially higher carbon (up to 0.45
wt-%), lower manganese (as low as 0.5
wt-%), lower oxygen (as low as 30 ppm)
and significantly higher nitrogen (up to
700 ppm) than found in weld metals produced by other arc welding processes.
Because of the unique chemical composition of FCAW-S weld metal, intermixing FCAW-S weld metal with
conventional arc weld metals can produce unexpected results. Thus, fabrication or repair procedures that result in
hybrid mixtures of different weld metal
types should be carefully considered
(Refs. 1, 2). A review of literature involving intermixing of FCAW-S welds and
welds produced using other processes revealed only two studies. In the first study,
Experimental Approach
Accordingly, a study was undertaken
to determine the intermixing effects on
Fill Electrode
E7018
4 mm (532 in.)
E7018-1
4 mm (532 in.)
Groove Welds
Root Electrode
Test Summary
E7018
AWT, CVN selected temp.
4 mm (532 in.)
and transition curve, chem.
analysis, metallography
E70T-4
AWT, CVN selected temp.
3 mm (0.120 in.)
and transition curve, chem.
analysis, metallography,
E70T-6
hardness/chem. profile
2.4 mm (332 in.)
E70T-7
2.8 mm (764 in.)
E70TG-K2
AWT, CVN selected temp.,
2.8 mm (764 in.)
chem. analysis
E71T-8
2 mm (564 in.)
E7018-1
AWT, CVN selected temp.
4 mm (532 in.)
and transition curve, chem.
analysis, metallography
E70T-4
AWT, CVN selected temp.
3 mm (0.120 in.)
and transition curve, chem.
analysis, metallography,
E70T-6
hardness/chem. profile
2.4 mm (332 in.)
E70T-7
2.8 mm (764 in.)
E70TG-K2
2.8 mm (764 in.)
E71T-8
2 mm (564 in.)
Cap Electrode
E7018
4 mm (532 in.)
E7018-1
4 mm (532 in.)
Bead-on-Plate Welds
Base Electrode
Test Summary
E70T-4
3 mm (0.120 in.)
E70T-6
2.4 mm (332 in.)
E70T-7
2.8 mm (764 in.)
E70TG-K2
2.8 mm (764 in.)
E71T-8
2 mm (564 in.)
Chem. analysis,
metallography
E70T-4
3 mm (0.120 in.)
E70T-6
2.4 mm (332 in.)
E70T-7
2.8 mm (764 in.)
E70TG-K2
2.8 mm (764 in.)
E71T-8
2 mm (564 in.)
Chem. analysis,
metallography
Chem. analysis
Chem. analysis
AWT (all weld tensile located at max. dilution), CVN at selected temperatures (impact tests for near surface, max. dilution and root locations), CVN transition curve
(impact tests to develop full transition curve for max. dilution location only), chemical analysis (at near surface and max. dilution locations in transverse section of groove
welds, in cap only for bead-on-plate welds), metallography (evaluation of microstructure in E7018 and E7018-1 fill and cap passes), hardness/chemical composition profile (microhardness and composition as a function of distance from the fill/root fusion boundary in groove welds).
Polygonal
Ferrite Grain
Hillards Circular
Intercept Line
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Electrodes
Fill
E7018
Root
E7018
AW
AG
E70T-4
AW
AG
E70T-7
AW
AG
E70T-6
AW
AG
E70TG-K2 AW
AG
E71T-8
AW
AG
E7018-1
AW
AG
E70T-4
AW
AG
E70T-7
AW
AG
E7018-1
E70T-6
AW
AG
E70TG-K2 AW
AG
E71T-8
AW
AG
UTS
(ksi)
78.3
77.6
80.0
79.3
82.6
81.3
82.0
81.4
80.5
79.8
80.1
81.8
YP
(ksi)
69.2
69.0
70.5
69.7
72.0
70.7
71.7
72.8
71.5
71.7
70.2
71.5
YS
(ksi)
64.2
63.7
64.4
63.4
67.0
64.7
67.5
67.2
66.1
64.5
65.7
66.5
EL
(%)
28
30
25
30
20
29
24
29
24
29
26
27
RA
(%)
74
73
61
74
43
72
63
77
63
73
55
70
Location
S
MD
S
MD
S
MD
S
MD
S
MD
S
MD
C
0.070
0.067
0.067
0.086
0.070
0.145
0.066
0.098
0.068
0.075
0.061
0.100
S
0.012
0.012
0.013
0.010
0.012
0.008
0.012
0.008
0.013
0.007
0.012
0.008
P
0.020
0.020
0.017
0.017
0.018
0.010
0.020
0.013
0.018
0.012
0.019
0.012
Si
0.54
0.54
0.51
0.56
0.53
0.30
0.56
0.34
0.52
0.44
0.52
0.45
Mn
1.08
1.07
1.05
1.08
1.10
0.72
1.08
1.35
1.06
1.17
1.06
0.90
Ni
0.03
0.04
0.03
0.03
0.03
0.02
0.03
0.02
0.03
0.51
0.03
0.02
Al
0.01
0.01
0.01
0.02
0.01
0.98
0.01
0.60
0.01
0.37
0.01
0.22
Ti
N*
0.001
0.002 90
0.001
0.001 85
0.002
0.002 111
0.001
0.028 105
0.002
0.002 90
0.002
0.021 110
79.3
80.7
83.1
83.1
83.3
84.2
81.8
82.4
81.2
80.1
83.1
83.8
73.8
73.6
72.6
76.0
74.6
73.0
75.5
76.0
73.6
72.5
76.7
77.4
67.2
67.0
69.1
69.4
70.1
71.1
68.2
66.7
67.2
67.0
69.7
70.1
26
28
29
30
19
29
30
30
29
30
28
28
77
70
74
76
39
73
76
76
71
77
74
71
S
MD
S
MD
S
MD
S
MD
S
MD
S
MD
0.059
0.063
0.060
0.089
0.061
0.123
0.061
0.067
0.060
0.063
0.060
0.075
0.014
0.013
0.013
0.011
0.014
0.009
0.013
0.012
0.013
0.012
0.014
0.012
0.012
0.013
0.013
0.012
0.014
0.013
0.013
0.013
0.013
0.013
0.012
0.011
0.52
0.53
0.53
0.56
0.53
0.57
0.53
0.54
0.53
0.53
0.53
0.51
1.37
1.36
1.37
1.37
1.40
1.32
1.39
1.45
1.34
1.37
1.37
1.27
0.04
0.04
0.04
0.04
0.04
0.03
0.04
0.04
0.04
0.13
0.04
0.03
0.01
0.01
0.01
0.04
0.01
0.13
0.00
0.03
0.01
0.02
0.01
0.04
0.009
0.010
0.009
0.013
0.009
0.015
0.009
0.011
0.010
0.010
0.010
0.013
O*
395
385
400
410
390
390
65 310
90 330
80 350
80 325
65 315
75 315
Si
Mn
Ni
Al
Ti
N*
O*
0.23
0.220.26
0.09
0.060.07
0.150.17
<0.003
<0.003
0.007
<0.003
<0.003
0.011
0.007
0.010
0.008
0.0050.007
0.28
0.100.11
0.250.26
0.190.22
0.290.30
0.500.52
0.430.45
1.41.5
1.21.4
0.530.69
0.02
0.01
0.01
1.21.4
0.01
1.52.0
1.52.0
0.71.0
1.11.5
0.50.7
<0.01
<0.01
0.04
<0.01
0.050.06
500700
550700
300400
230350
200350
4070
7080
450550
6080
250340
Base
Electrode
Dilution
(%)
Si
Mn
Ni
Al
Ti
N*
O*
E7018
E70T-4
E70T-7
E70T-6
E70TG-K2
E71T-8
29
29
35
34
25
0.113
0.114
0.070
0.068
0.090
0.008
0.008
0.009
0.007
0.008
0.009
0.008
0.009
0.008
0.008
0.52
0.52
0.43
0.47
0.45
1.08
1.07
1.16
1.20
1.04
0.05
0.05
0.05
0.35
0.05
0.21
0.18
0.09
0.16
0.09
0.002
0.002
0.005
0.002
0.006
125
200
145
135
155
325
285
505
390
470
E7018-1
E70T-4
E70T-7
E70T-6
E70TG-K2
E71T-8
31
30
33
33
37
0.113
0.116
0.074
0.064
0.087
0.008
0.008
0.010
0.009
0.010
0.013
0.011
0.010
0.011
0.010
0.58
0.56
0.48
0.54
0.48
1.34
1.30
1.19
1.43
1.19
0.03
0.03
0.03
0.35
0.03
0.22
0.19
0.13
0.17
0.10
0.013
0.016
0.013
0.012
0.013
250
200
205
220
145
255
260
395
320
405
FCAW-S root passes. The specimen locations were recorded to facilitate removal
of comparable specimens from the
E7018 and E7018-1 baseline welds. Five
CVN impact tests were conducted at
each of two temperatures, 18C and
29C (0F and 20F) for all combinations at the near surface and maximum
dilution locations. Most root specimens
were tested at these same test temperatures. The exception is for the E70T-4
root, which was tested at room temperature and 0C (32F).
Chemical analysis was conducted at
both the near surface and maximum dilu-
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(A)
(B)
composition as a
function of distance from the
S M AW / F C AW- S
fusion boundary.
Bead-on-Plate
Welds
To more clearly
identify
the
changes in chemical composition
and microstructure occurring in
Fig. 8 Effect of intermixing on Charpy fracture appearance (uniform
deformation typical of CVN fractures on the right, nonuniform deforma- the first layer of
SMAW deposited
tion typical of intermixed weld metal on the left).
over each of the
FCAW-S deposits,
welds, the SMA weld metals are exbead-on-plate welds were prepared for
pected to have chemical compositions
each SMAW/FCAW-S combination. Dinominally different than those deposited
lution from the base plate was minimized
over SMA root passes. Specifically, for
by gouging troughs into a 25-mm (1-in.)
some root and fill electrode combinathick plate and filling them with two laytions, increases in aluminum, carbon and
ers of FCAW-S. The weld reinforcements
nitrogen concentrations (as well as dewere machined flush with the base
creases in manganese concentrations)
plates. A single bead of SMAW was dewere expected. Thus, it was important to
posited on each, using the same welding
measure the extent of these dilution efprocedure employed for the multipass
fects. The chemical composition gradiwelds. FCAW-S and SMAW electrodes
ent in the intermixed weld metal above
for the base and cap passes, respectively,
the SMAW/FCAW-S fusion boundary was
were from the same production runs used
determined by successive sectioning.
for the multipass welds. Samples were reChemical analysis by optical emission
moved from each of the ten welds for
spectroscopy was conducted on longitumetallographic examination and chemidinal sections parallel to the top surfaces
cal analysis, using the same techniques
of the test welds and above the fusion
employed for the groove welds. In addiboundaries. The first analysis was contion, oxygen and nitrogen analyses were
ducted at an approximate distance of 45
conducted by inert gas fusion, followed
mm (0.1570.197 in.) from the fusion
by infrared and thermal conductivity deboundary. This allowed the entire area
sampled in each analysis to be located at
tection, respectively.
a consistent elevation relative to the fuMetallographic Examination
sion boundary. Successive grinding operations between analyses permitted
Detailed metallographic evaluation
determination of the weld metal chemical
was limited to the intermixed combinations for which full CVN transition curves
were developed. These included E7018/
E70T-4, E7018/E70T-6, E7018-1/E70T-4,
E7018-1/E70T-6 and the corresponding
baseline welds fabricated entirely with
E7018 and E7018-1. Two types of samples were characterized transverse
sections from multipass welds and transverse sections from bead-on-plate welds.
One sample of each type was provided
for each intermixed combination. The experimental weld metals were prepared for
optical and scanning electron microscopy (SEM) evaluation by sectioning the
welds normal to the welding direction,
grinding and polishing through 1 m. Following specimen preparation, the polished surfaces were etched by immersion
in a 2% nital solution for approximately
1520 s. Photographs of the weld metal
microstructures were taken at magnifications of 200, 400 or 1000X. SEM was used
for higher magnification examinations.
Regions corresponding to the various
CVN locations (near surface, maximum
dilution and root) were marked on the
multipass samples to allow for easy identification of the respective regions. The
balance of root weld metal and fill weld
metal were measured in the region of
maximum dilution. Additionally, the relative amounts of primary weld metal and
reheated weld metal in the maximum dilution and near-surface regions were
measured at magnifications of 1040X.
Due to the heterogeneous nature of
weld metal microstructures produced
during multipass welding, characterization of microstructures found at the CVN
locations using the conventional IIW
method (Ref. 7) was not practical. Since
the microstructures in these regions are
composed of a wide range of microconstituents with a range of shapes and sizes,
(A)
(A)
50 m
(B)
50 m
(B)
50 m
(C)
50 m
(C)
50 m
Fig. 11 Microstructures observed in the
maximum dilution region in E7018 weld
metal deposited over: A E7018; B E70T4; and C E70T-6.
50 m
Fig. 12 Microstructures observed in the
maximum dilution region in E7018-1 weld
metal deposited over: A E7018-1; B
E70T-4; and C E70T-6.
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Fig. 13 Apparent grain size measured in the first layer, second layer
and top surface of the E7018 weld metal deposited over the various root
electrodes.
Fig. 14 Apparent grain size measured in the first layer, second layer
and top surface of the E7018-1 weld metal deposited over the various
root electrodes.
in the case of dilution from E70T-7. However, there is a relatively small reduction
in ductility in the as-welded condition
as a result of dilution in all of the E7018
deposits. Some hydrogen effects (such as
small fisheyes and hydrogen flakes) were
observed in the fractured tensile specimens from these welds. This effect was
most pronounced in E7018 and E7018-1
weld metal deposited over the E70T-7
root layers. Comparing results of the
E7018/E70T-7 ductility with the E7018
baseline weld, elongation decreased
from 28 to 20% and the reduction in area
decreased from 74 to 43%. Similarly, for
the E7018-1/E70T-7 compared with the
E7018-1 baseline weld, elongation decreased from 26 to 19% and the reduction in area decreased from 77 to 39%.
All evidence of hydrogen effects was
eliminated after a standard aging treatment. In general, dilution from the
Table 5 Relative Fractions of Root/Fill at Root Charpy Locations, Relative Fractions of Primary/Retransformed Metal at Maximum Dilution
and Near Surface Charpy Locations
Root Electrode
Fill
Max. Dilution
Top Surface
Root
Sample ID
% Root
% Fill
% Primary
% Retransformed
% Primary
% Retransformed
E7018-1
E70T-4
E70T-7
E70TG-K2
E70T-6
E71T-8
E7018-1
PV504
PV495
PV492
PV509
PV517
PV524
70
67
60
50
50
N/A
30
32
40
50
50
N/A
20
7
14
7
15
9
80
93
86
93
85
91
13
25
17
18
8
20
87
75
83
82
92
80
E7018
E70T-4
E70T-7
E70TG-K2
E70T-6
E71T-8
7018
PV488
PV476
PV478
PV470
PV473
PV483
56
60
62
65
62
N/A
44
40
38
45
38
N/A
8
3
5
3
5
7
92
97
95
97
95
93
24
3
11
13
5
2
76
97
89
87
95
98
(A)
(A)
50 m
(B)
10 m
(B)
50 m
(C)
10 m
(C)
10 m
50 m
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Considering the
results of chemical
analyses taken in
the transverse cross
sections summarized in Table 2, it
became clear that
reliable and consistent measurement
of chemical comFig. 17 Bead-on-plate microstructures quantified in the E7018-1 weld position of SMA
metals deposited over the indicated root electrodes.
weld metal directly
above the FCAW-S
root was difficult.
FCAW-S and SMAW in these specimens
In many cases, it appeared that the chemwere reasonably consistent, it can be
ical composition of the SMA weld metals
concluded that any toughness changes
did not change significantly, when comoccurring at the root location were not
pared to the undiluted SMA weld metals.
strongly influenced by the minor differFor example, the increase in Al at the
ences in the proportions of root and fill
maximum dilution location is not consisweld metals. While the potential causes
tent for E7018 and E7018-1 deposits over
of reduced toughness measured in the
the same FCAW-S root. Some of these inroot specimens were not examined in
consistencies arise from the difficulty in
great detail, some preliminary concluprecisely locating a 6-mm (0.25-in.) disions can be drawn from the results. In
ameter target for emission spectroscopy
the case of the SMAW electrodes deat the required location in the transverse
posited over E70T-4 and E70T-7 FCAW-S,
weld cross sections. Another reason for
the reduced toughness of the composite
such unexpected results is that the diluCVN specimen is consistent with the
tion effects did not extend much past the
lower toughness typically achieved in
first layer of SMAW deposited, while the
E70T-4 and E70T-7 weld deposits. This
analytical techniques employed measure
suggests that the lower toughness matethe composition of a much larger area
rial in the composite specimens is prethan one weld layer. Any potentially sigdominantly responsible for performance
nificant changes in composition of the
of the entire specimen. It is important to
first layer would be masked by the avernote that minimum levels of toughness
aging effect of the larger sample area,
are not required for weld deposits proproviding that the sample area was on
duced with E70T-4 or E70T-7 electrodes
target.
(Ref. 6). Lower than expected toughness
Consequently, two alternative apalso was measured in composite speciproaches were taken to determine the
mens containing the SMA weld metal
chemical composition of the SMA weld
and E70T-6, E70TG-K2 and E71T-8. In
metal in the region of maximum dilution.
these cases, the toughness exhibited by
First, chemical analysis was conducted
the composite CVN specimens was typion longitudinal sections parallel to the
cally lower than the toughness expected
top surfaces of the test welds and above
for the respective individual weld metals.
the SMAW/FCAW-S fusion boundaries
In several cases, the toughness measured
using emission spectroscopy. These refor the composite specimens was on the
sults are presented in Figs. 9 and 10 for
same order as the toughness measured
each of the SMAW electrodes deposited
for the maximum dilution locations in the
over E70T-4 and E70T-6 FCAW-S roots.
same welds. This suggests that the diluted
The second approach was to examine
SMA weld metal had a strong influence
the composition of a single E7018 or
on the toughness exhibited by the root
E7018-1 bead deposited over the various
CVN specimens from these welds. VerifiFCAW-S deposits in the bead-on-plate
cation would require additional study, inconfiguration previously described. This
cluding fractographic analysis of the
permitted analysis of a single bead repbroken specimens. The evidence sugresenting maximum dilution without ingests that the toughness in the root specterference from subsequent weld passes.
results of the apparent grain size measurements are shown graphically in Figs.
13 and 14. Figure 13 shows that microstructural refinement occurred in the
E7018 weld metal up to the near surface
regions when diluted with either FCAWS root material. In contrast, Fig. 14 seems
to indicate that E7018-1 weld metal experiences very little change in grain size.
Examination of microstructures in the
second layer up from the E7018-1/E70T4 and E7018-1/E70T-6 boundaries revealed that the effects of dilution with the
FCAW-S root deposits had essentially disappeared. The microstructures at this location were essentially identical to those
found in undiluted E7018-1 weld metals.
Normally, the best way to obtain a
combination of high strength and high
toughness is through grain refinement.
The classical model of cleavage fracture
suggests that cleavage occurs at a temperature where the yield strength exceeds the fracture stress. Considering that
the fracture stress and yield stress both increase with decreasing grain size, increased toughness was expected in these
samples. It is apparent that the toughness
increase normally experienced with
grain refinement is being offset in the
intermixed weld metals by some other
factor.
In some cases, toughness can be decreased by the presence of high-volume
fractions of second-phase carbides, M-A
constituent or pearlite colonies that form
either intergranularly or along grain
boundaries. To verify if toughness was
detrimentally influenced by increased
second-phase volume fractions, the
weld metals found in the region of maximum dilution were examined at higher
magnifications using SEM. Figure 15
shows carbide films and M-A constituents found in the maximum dilution location of undiluted E7018-1
weld metal and the maximum dilution
locations in E7018-1/E70T-4 and E70181/E70T-6 intermixed weld metals. It is
apparent that the volume fraction of carbide films in the undiluted E7018-1
weld metal was comparable to that
found in the E7018-1/E70T-4 and
E7018-1/E70T-6 weld metals. Similar
behavior was found in the E7018 weld
metals. Point counting at higher magnifications revealed that the amount of
second phase measured in the intermixed weld metals was no more than
24% higher than that found in the undiluted weld metals. For both fill electrodes, it should also be noted that the
SMA weld metal deposited over the
E70T-6 appeared to be dirtier (contained more inclusions) than compara-
RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT
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shielded flux cored electrodes part II. Welding Journal 51(4): 138-s to 155-s.
16. Kaplan, H. I., and Hill, D. C. Thermodynamics of air-operating flux cored electrodes and an analysis of weld toughness.
1976. Welding Journal 55(1): 13-s to 19-s.
17. Kluken, A. O., and Grong, . 1989.
Met. Trans. A 20A, pp. 13351349.
18. Grong, , Kluken, A. O., and Bjrnbakk, B. 1988. Joining and Materials 11(4):
164169.
19. Evans, G. M. 1983. The effects of stress
relief on microalloyed weld metal impact
properties. Welding Journal 62(11): 313-s to
320-s.
20. Svensson, L-E., and Gretoft, B.
1990.Microstructure and impact toughness of
C-Mn weld metals. Welding Journal 69(12):
454-s to 461-s.
21. Abson, D. J. 1979. Welding Research
International 9(5): pp. 122.
8
42
The nature and the effect of the unmixed zone in dissimilar fusion welds, especially its significance with regard
to corrosion resistance, has been studied in this Welding Research Council-sponsored program. Three types of
super-austenitic stainless steel (high Mo) (AL-6XN, 254SMO and 654SMO) and five types of fully austenitic nickelbased weld filler metals (Inconel 625, C-22, C-276, 686CPT and P16) were evaluated. Shielded metal arc (SMA),
gas metal arc (GMA), gas tungsten arc (GTA) (filler added) and gas tungsten arc (GTA) autogenous welding
processes were used for fabricating weldments of each superaustenitic stainless steel. The employment of these
welding techniques provided a full range of unmixed zone formation.
The unmixed zone formation was metallographically evaluated using both optical light microscopy (OLM) and
scanning electron microscopy (SEM) with varied etchants and etching techniques.
The pitting corrosion behavior of the unmixed zone was evaluated using immersion corrosion tests in 10%
FeCI3.
Publication of this document, WRC Bulletin No. 428, was sponsored by the Welding Research Council, Inc.
The price of WRC Bulletin 428 (January 1998, 98 pages) is $110.00 per copy plus $5.00 for U.S. and Canada
and $10.00 for overseas postage and handling. Orders should be sent with payment to the Welding Research
Council, 3 Park Ave., 27th Floor, New York, NY 10016-5902. Phone (212) 591-7956; Fax: (212) 591-7183;
e-mail: wrc@forengineers.org or visit our homepage at http://www.forengineers.org/wrc.
RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT/RESEARCH/DEVELOPMENT
Acknowledgment