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Inconel 625 Welding Metallurgy

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  • 8/11/2019 Inconel 625 Welding Metallurgy

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    The Welding and Solidif ication Metallurgy

    of Alloy 625

    Chemical composition and solidification microstructure are

    correlated to hot cracking susceptibility

    BY M . J. CIESLAK

    ABSTRACT. The weld metal microstruc

    tu re deve lopment and

    solidification

    crack

    ing behavior o f Al loy 625 gas tungsten arc

    (GTA) we lds as a funct ion o f comp osi t ion

    has been determined. A th ree-factor , tw o-

    level,

    factoria l ly-designed set of a l loys in

    volv ing the elements C , Si and Nb was ex

    amined.

    Differen tia l therm al analysis (DTA)

    of these al loys indicated that N b, and to a

    lesser exten t C a nd

    S i,

    increased the melt

    ing /so l id i fica t ion tem pera ture range. The

    DTA revealed that terminal sol id if ication

    const i tuents were f o rm ed in the Nb-bear-

    ing al loys, the presence of which was

    conf i rm ed by opt ica l and e lectron micros

    cop y techn iques and ident i fied as 7 / M C -

    (NbC) carb ide , 7 /Laves and 7/M

    6

    C car

    bide eutectic-type consti tuents. Addit ion

    of carbon to the Nb-bearing al loys was

    observed to promote the fo rmat ion o f

    th e

    7 /MQNbC)

    carbide co nsti tuent an d Si

    was observed to promote increased fo r

    mat ion o f the 7 /Laves const i tuent . Re

    gression analysis of Varestraint hot-crack

    testing data revea led that addit ions of C o r

    Si to A lloy 625 increase d the s uscep tibility

    o f the a l loy to ho t cracking . N iob ium-free

    a l loys wer e obse rved to have a very low

    tendency toward so l id i f ica t ion hot crack

    ing,but even amo ng these al loys, C and Si

    addit ions were detrimental. I t was con

    cluded that the increased sol id if ication

    tempera ture range and fo rmat ion o f Nb-

    rich eutectic consti tuents were primari ly

    responsible for the increased susceptib i li ty

    of N b-bearing al loys to

    solidification

    crack-

    Introduction

    Al loy 625 (58 min imum Ni-20-2 3 Cr, 8 -

    10

    M o , 3 .15 -4 .15 Nb+T a -5 m ax imum Fe -

    0 .5 maximum M n, 0 .5 m aximum Si, 0 .10

    maximum C wt-%) has been a commonly

    used nickel-based al loy for over two de-

    M.J. CIESLAK iswithSandia NationalLaborato

    ries,

    Albuquerque,

    N.Mex.

    Paper presented at the 68th Annual AWS

    Meeting, held March 22-27,

    1987,

    in Chicago,

    III.

    cades. Although orig inal ly developed as a

    turbine al loy (Ref. 1), i ts com bina tion of

    good oxidation and corrosion resistance

    and moderate mechanical strength have

    made it a successful alloy in many other

    applications. Among these are cladding

    and surfacing for marine environments

    (Refs.

    2, 3) and for wear resistance as

    hardfacing for tool and die steels (Ref. 4).

    Al loy 625 is not without i ts problems,

    though. Recent studies (Refs. 5, 6), have

    indicated that th is al loy can be susceptib le

    to hot cracking. Patterson and Milewski

    (Ref. 5) no ted that ho t crac ked surfaces in

    arc we lds made between A l loy 625 and

    304L stainless steel w er e e nric hed in

    S,

    Nb ,

    P and C, and that

    eutectic-like

    structures

    were present in the microstructures of

    these welds . Cieslak,

    etal.

    (Ref. 7), found

    that dissimilar metal

    CO2

    laser beam w elds

    between Inconel Al loy 625 and 304 stain

    less steel made at slow travel speed (10

    in./m in) con tained a Nb-ric h Laves phase.

    A l though in compar ison to many o ther

    nickel alloys (Refs. 8, 9), Alloy 625 has a

    good reputation for resistance to hot

    cracking, i t appears fro m the l i terature no t

    to be to ta l ly immune f rom the prob lem.

    A review of the l i terature reveals no

    published study that correlates the sol id i

    f ication microstructure with weldabil i ty in

    Alloy 625 as a function of chemical com

    posit ion. In addit ion, no published report

    describes the sequences of sol id if ication

    events leading to the development of the

    K E Y W O R D S

    Microstructure Deve lopment

    Solid if ication Crack

    GTA Al loy 625 Welds

    Differentional Analysis

    Thermal Analysis

    Eutectic Constituent

    7 /Laves Const i tuents

    7 / M C Ca rb ide

    7/M6 Carbide

    Nb-Containing Alloys

    observe d microstructure in A l loy 625, The

    purpose o f th is work,

    then,

    i s two fo ld .

    First, the welding metal lurgy of Al loy 625

    is described in some de tai l . That is, the ev

    o lu t ion o f we ld meta l microstructure upon

    cooling from the l iquidus is explained.

    Second, a correlation is establ ished be

    tween al loy chemistry and both sol id if ica

    t ion microstructure and weldabil i ty (hot-

    cracking s usceptib i l ity). These results may

    provide for intel l igent al loy optimization

    schemes for Al loy 625 and similar materi

    a ls from a weldabil i ty perspective.

    Exper imental Procedure

    The al loy design decision for th is ex per

    iment was driven by the desire to estab

    l ish the fundam ental s ol id if ication and ho t-

    cracking mechanisms in th is al loy system.

    The e f fect o f t ramp e lements (S,P, B, etc .)

    on the sol id if ication and weldabil i ty be

    havior of n ickel-based al loys has been w ell

    establ ished. It was concluded that study

    ing these e lements wou ld no t add much

    new insigh t . They were e l iminated f rom

    this study by being held at constant low

    levels. Also, i t had been observed earl ier

    (Ref. 10) that the solidificatio n m icros truc

    ture in Alloy 625 and similar alloys could

    conta in minor const i tuents composed o f

    Laves phase and MC carbide. Both of

    these phases we re N b-rich a nd Laves had

    been shown (Ref .

    11)

    to be stabi l ized by

    Si alloying additions. Based upon these

    tw o factors, C, S i and Nb we re chosen as

    the composit ion variables for th is experi

    ment .

    A three-factor, two-level factoria l series

    of a l loys was designed around these ele

    ments. The aim low level for C, 0.005 wt-

    %, was effectively the l imit of industria l

    processing capabil i ties. The high level for

    C was set at what would l ikely be ex

    pected in a high C commercial heat of Al

    loy 625, 0.035 wt-%. The low level for Si

    was set as none intentionally added. The

    high level a im was 0.35 wt-%. The low

    level for Nb was set as none intentionally

    added. The high level a im was 3.5 wt-%.

    The levels for Nb would clearly indicate

    the d i f fe rence between Nb-bear ing and

    WELDING RESEARCH SUPPLEMENT

    149-s

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    Table 1 -

    Element

    C

    M n

    P

    5

    Si

    Cr

    M o

    Ti

    N b

    Fe

    Ni

    -Al loy Composit ions

    1

    0.006

    0.02

    0.005

    0.002

    0.03

    22.10

    9.54

    0.06

    0.01

    2.56

    bal

    2

    0.031

    0.02

    0.005

    0.002

    0.03

    21.95

    9.61

    0.06

    0.01

    2.55

    bal

    ( w t - % )

    3

    0.006

    0.02

    0.005

    0.002

    0.35

    21.63

    9.60

    0.06

    0.02

    2.18

    bal

    A l l oy Number

    4

    0.036

    0.03

    0.005

    0.003

    0.39

    21.57

    9.63

    0.06

    0.02

    2.59

    bal

    5

    0.009

    0.03

    0.006

    0.003

    0.03

    21.81

    9.81

    0.06

    3.61

    2.30

    bal

    6

    0.038

    0.03

    0.006

    0.003

    0.03

    21.83

    9.81

    0.06

    3.60

    2.31

    bal

    7

    0.008

    0.03

    0.006

    0.004

    0.38

    21.65

    9.68

    0.06

    3.57

    2.26

    bal

    8

    0.035

    0.03

    0.006

    0.003

    0.46

    21.68

    9.67

    0.06

    3.53

    2.29

    bal

    Nb-free alloys. The alloys were double

    vacuum melted at the Sandia Nat ional

    Laborator ies melt ing and solidif icat ion fa

    cility. Init ial melting was done in a vacuum

    induct ion furnace from virgin raw mater i

    als.

    Electrodes weighing approximately

    15 0Ib (68.2 kg) were poured in vacuum.

    These electrodes were then vacuum arc

    remelted to 6- in. (152-mm) diameter in

    gots in preparat ion for hot working. Table

    1 lists the compositions of the eight alloys

    studied.

    Hot working of the ingots began with

    extrusion at 117 5C (2147F) do w n to a

    3-in.

    (76-mm) diameter bar. These bars

    we re then f la t tened at

    1175C

    to app rox

    imately 0.6-in. plates. From these plates,

    specimens were taken for dif ferent ial ther

    mal analysis (DTA). The plates were fur

    ther reduced by hot rol l ing (1175C) to a

    thickness of ap proxim ately 0.18 in. (4.6

    mm).Further reduct ion was done at room

    temperature to a thickness of approxi-

    Alloy

    S ( Mb

    O N

    HEATING

    O N C O O L I N G

    mately0.12 in. (3 mm). These sheets w ere

    given a final anneal at 1010C (1850F)

    and water quenched. A cold straightening

    pass ( < 1 % co ld work) was then made to

    prepare the sheets for machining into

    Varestraint test specimens.

    The autoge nous gas tungsten arc (GTA)

    Varestraint test was used to quant ify the

    suscep tibility of these alloys tofusionzone

    hot cracking. The GTA welding parame

    ters used were 100 A, (direct current,

    electrode negat ive at a t ravel speed of 8

    i n . /m in .

    The machine voltage was ra 12 V

    and argon was used as the shielding gas.

    These condit ions produced welds that

    were approx imate ly 0.20 in . wide at the

    top surface. The test specimens measured

    ra 6.5 X ra 1 X ra 0.12 in . (165 X 25 X

    3 mm). All tests we re p erf orm ed at a strain

    level of ra 2.5% to simulate high restraint

    we lding c ondit ions. R eplicate test ing (4 to

    5 tests per alloy) was employed to de

    velop acceptable stat ist ics. The order of

    test ing was randomized to eliminate sys

    tematic error. Maximum crack length

    (MCL) was the quant itat ive measure of

    hot-cracking susceptibility used in this

    study.

    Differential thermal analysis (DTA) test-

    A l l o y 6 ( N b . C )

    O N H E A T I N G O N C O O L I N G

    , 0 0 0 1 * 0 0

    1 0 0

    TEMPERATURE C)

    Fig.

    1-DTA

    thermogram

    (20 C/min)

    for Alloy

    5.

    TEMPERATURE (C)

    Fig.

    2-DTA thermogram 20

    C/min)

    for Alloy

    6.

    ing was done on a Netsch thermal ana

    lyzer STA 429. Samples were machined

    f rom blocks taken f rom the hot -worked

    plates that had been subsequent ly an

    nealed in vacuum at1200C (2192F) for

    4 h and water quenched. The samples

    weighed ra 0.8 g. All tests were con

    ducted in a hel ium environm ent w i th pure

    W used as the reference mater ial. To

    cal

    ibrate the system, pure Ni was found to

    melt wi th in 2C (3.6F) of the established

    literature value. The experiments involve d

    heat ing and cooling the Nb-bearing alloys

    (Alloys 5-8) through the melt ing/solidif i

    cat ion temperature range as fast as was

    possible(20 C/m in 36F/min) wi th the

    available equ ipme nt. The purpose of these

    experiments was to ident ify any terminal

    solidif icat ion react ions that were occur

    ring in these alloys.

    Varestraint test and DTA specimens

    were examined metallographically. After

    polishing through 0.05

  • 8/11/2019 Inconel 625 Welding Metallurgy

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    Results

    The DTA thermograms obta ined f rom

    Alloys 5-8 are shown in Figs. 1-4. The al

    loys containing C at the high level (6, 8)

    show an event prior to matrix melt ing,

    which is l ikely the dissolution of Nb car

    bide. The high-tem peratu re annealing (4 h

    at 1200C) was insuff icient to dissolve

    these stable carbides. Figure 5 shows the

    Nb carbides present in the microstructure

    of Al loy 6 prior to DTA testing. The

    solid

    i f ication behavior of Al loys 5-8 can be

    seen by examination of the individual

    thermograms. A l loys 5 and 6 show two

    exothermic events, while Al loys 7 and 8

    show three exothermic events.

    The results of Varestraint test experi

    ments are shown in Fig. 6. As can be

    readily seen, the hot-cracking susceptib i l

    i ty under these test condit ions is greater

    forthe Nb-b earing al loys (5-8) than for the

    Nb-free al loys (1-4).

    The microstructures observed in the

    GTA weld metals could be easi ly d iscrim

    inated on the basis of Nb content. Al loys

    1-4 had microstructures that were essen

    tially single phase and will not be further

    discussed in th is paper. Al loys 5 -8 had mi

    crostructures that contained minor inter

    dendrit ic consti tuents in addit ion to the

    dendrit ic m atrix. As a general observ ation,

    Alloy 5 had the smallest minor consti tuent

    population and Alloy 8 had the greatest

    amount o f minor const i tuent . No a t tempt

    was made to further quantify th is obser

    vation in the weld metal. I t had been

    shown earlier (Ref. 16) that the DTA sam

    ples had bet we en 0.3% (Alloy 5) and 1.3%

    (Alloy 7) by volume of minor consti tuent.

    The SEM exam ination of Varestraint test

    samples from Alloys 5-8 revealed that

    these interdendrit ic consti tuents were as

    socia ted wi th the fo rmat ion o f fusion

    zone hot cracks. As a represe ntative ex

    ample of these ob servation s, Fig. 7 (A, B)

    shows the microstructure associa ted wi th

    a fusion zone hot crack in Al loy 7.

    Identif ication of these phases was ac

    compl ished by perfo rming se lected-area

    electron diffraction on th in fo i ls and ex

    t ract ion rep l icas made f rom the Vare

    straint test samples. The primary micro-

    consti tuents ob ser ve d wer e a Laves phase

    (hexagonal, a ra 0.476 nm , c ra 0.713 nm)

    and MC carbide (cubic, a ra 0.441 nm).

    The observations made in examination of

    the th in fo i ls we re cons istent with t he SEM

    examination of the Varestraint test sam

    ples relative to minor consti tuent popula

    t ion. That is, Al loy 5 had a much lower

    vo lume f ract ionofm inor const i tuent than

    did Alloys 6- 8. In addit ion t o the Laves and

    MC carb ide phases observed, A l loy 7

    (high Nb, Si) was found to contain a

    coarsely lamellar M

    6

    C carb ide (d iamond

    cubic, a=a 1.12 nm) constituent on its ex

    t ract ion rep l ica . Tw o morpho log ies o f MC

    wer e observed, a dendr i t ic o r Ch inese-

    scr ip t morp ho logy and a smaller b locky

    O N HE AT I NG

    Al l o y 7 No.SO

    A l l o y a Nb .C.S i )

    O N C O O L I N G

    T E M P E R A T U R E ( C )

    Fig. 3

    DTA

    thermogram 20

    C/min)

    for Alloy

    7.

    morpho logy .

    It was qualitatively observed (Ref. 16)

    tha t the predominant microconst i tuent in

    Alloys 5 and 7 was Laves, whereas for Al

    loys 6 and 8, it was M C carbide. In the case

    of Al loy 8, large quantit ies of both MC

    carbide and Laves we re o bse rved . Figures

    8A and 8B are representative TEM micro

    graphs from Varestraint specimens show

    ing M C carbide (A lloy 6) and Laves phase

    (Alloy

    7),

    respectively. Table 2 summarizes

    the phases identif ied during the TEM

    anal

    yses.

    Two types o f e lementa l segregat ion

    were observed in the GTA weld meta ls.

    The f irst was the discontinuous composi

    t ion changes associated with the micro-

    const i tuents observed. The second was

    the periodic pattern of dendrit ic segrega

    tion associated with the sol id if ication pro

    cess.

    Using AEM techniques, as described

    above, the composi t ions o f the var ious

    phases in the weld metals of Al loys 5-8

    we re determ ined. These are l is ted in Ta

    ble 3. In the cases of the carbide phases,

    a composi t ion w as ca lcu la ted based upon

    ideal stoichiometry (MC or M

    6

    C). As can

    TEMPERATURE C)

    Fig. 4DTA thermogram 20 C/min) for Alloy

    be seen, al l of the microconsti tuents are

    enriched in Nb and depleted in Ni re lative

    to the nominal composit ions.

    The periodic dendrit ic segregation pat

    tern representative of the GTA welds

    made on the Nb-b earing al loys is shown in

    Fig. 9 (Al loy 7). What is observed is the

    enrichment of Ni and Fe in dendrite core

    (DC) regions and the segregation of Nb,

    M o a nd Si to inte rdendr it ic (ID) regions.

    There is very l i t tle dendrit ic segregation o f

    Cr

    observed in th is or any of the other al

    loys. Car bon co uld not be analyzed by th is

    techn ique because o f i ts low concentra

    t ion. The interdendrit ic consti tuents asso

    cia ted wi th ho t cracks in A lloys 5-8 wer e

    also chemically analyzed with the electro n

    microprobe. The results of these analyses

    are given in Table 4. All constituents are

    enr iched in bo t h Nb and M o re la t ive to the

    nominal a l loy composit ions and the

    c o n

    sti tuents obse rved in the high-Si heats (7

    8) are enriched in Si.

    Table 2Phases Observed in the TEM

    Al loy No.

    5 (Nb)

    6 (Nb, C)

    7 (Nb, Si)

    8 (Nb, C, Si)

    Thin Foil

    Laves

    (a)

    Small MC (NbC) carbides at

    7/Laves interface

    Dendri t ic MC (NbC)

    (a)

    Laves

    ,a)

    Small MC (NbC) carbides at

    7/Laves interface

    Dendri t ic MC (NbC)

    (a)

    Laves in vicinity of M C (N bC)

    Small MC (NbC) carbides at

    7/Laves interface

    Extraction Replica

    Dendr i t i c MC

    (NbC)

    (a

    >

    Blocky MC

    Laves

    Dendrit ic MC (NbC)

    Blocky

    MCW

    Thin Foi l /

    Extract ion

    T.F.

    Extr.

    Extr.

    Extr.

    T.F.

    Extr.

    Extr.

    Extr.

    T.F.

    Extr.

    Extr.

    from AEM Analysis

    C

    12.1

    11.6

    11.9

    12.4

    2.8

    12.3

    12.2

    12.2

    Ni

    45.6

    (0.2)

    3.3

    (0.1)

    0.1

    (0.1)

    2.1

    (0.1)

    48.2

    (0.2)

    2.5

    (0.1)

    31.6

    (0.2)

    3.5

    (0.1)

    46.7

    (0.2)

    4.5

    (0.1)

    4.1

    (0.1)

    Fe

    1.4

    (0.1)

    0.3

    (0.1)

    0.0

    0.1

    (0.1)

    1.0

    (0.1)

    0.3

    (0.1)

    0.5

    (0.1)

    0.0

    0.9

    (0.1)

    0.4

    (0.1)

    0.4

    (0.1)

    C r

    15.6

    (0.6)

    4.1

    (0.2)

    1.3

    (0.1)

    4.1

    (0.2)

    13.9

    (0.5)

    8.6

    (0.4)

    14.6

    (0.6)

    7.4

    (0.4)

    13.6

    (0.5)

    5.2

    (0.2)

    5.1

    (0.3)

    N b

    19.2

    (0.3)

    73.4

    (1.2)

    82.6

    (1.1)

    65.5

    (0.8)

    18.2

    (0.3)

    69.7

    (1.1)

    31.0

    (0.5)

    68.5

    (1.1)

    16.8

    (0.2)

    60.0

    (0.8)

    65.0

    (1.2)

    M o

    18.2

    (0.3)

    7.2

    (0.3)

    4.4

    (0.1)

    16.3

    (0.2)

    17.6

    (0.2)

    6.5

    (0.2)

    18.7

    (0.3)

    8.2

    (0.3)

    19.8

    (0.3)

    17.7

    (0.3)

    13.2

    (0.4)

    Si

    < 0 . 1

    0.0

    0.0

    0.0

    1.2

    (0.1)

    0.0

    0.9

    (0.1)

    0.0

    2.2

    (0.1)

    0.0

    0.0

    (a) Absolute error, wt-%.

    (b) Calculated assuming ideal MC stoichiometry.

    (c) Calculated assuming idealMeCstoichiometry.

    Table 4 -

    Alloy

    N o

    5

    6

    7

    8

    -Compositions of Constituents Associated with Hot Cracks

    N b

    17.45


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