xray residual stress

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    Beth Matlock, Senior Materials Engineer

    Materials Testing Division

    Technology for Energy Corporation (TEC)

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    History

    1974 Pre-Med Student Working at JC Penney Converted a scissor sale into a career

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    Dreams

    New Corvette My own horse - On my own farm Be self-sufficient

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    Background

    NCSU XRD for element and compoundanalysis, developed Co-Ga-B ternary diagram

    B&W XRD pole figures on Zr-4, failureanalysis, B4C research

    TEC XRD residual stress and retainedaustenite measurements, diffractometer design

    and development

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    What are Residual Stresses?

    Residual stresses are stresses that remain in the materialafter all external loads are removed. They result fromdifferential cooling rates (welding, heat treating, etc.) andplastic flow (shot peening, cold working, etc.)

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    How Do They Differ from Loading

    Stresses?

    Loading stress results from applied load: weight, torsion,

    bending, pressure, pushing, pulling, etc.

    You can measure total stress (residual stress and loading

    stress) using x-ray diffraction

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    Whats so Great about X-ray Diffraction

    Residual Stress Measurements?Nondestructive* surface measurement technique

    Measures strain, stresses are calculated

    Gives absolute stress value

    Measures residual strain if sample is unloaded

    If component is loaded, resultant stress will be the residual plus applied stress

    Measurements can be made on most metals and ceramics; samples must be polycrystalline with

    relatively randomly oriented medium to fine grains

    Measurements can be made in a few minutes to an hour

    *Depth profiling can be destructive Large samples need to be sectioned if using conventionalequipment

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    History of Residual Stress by X-ray

    Diffraction Techniques

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    Why Are Residual Stresses Important?

    Residual stresses may be harmful or beneficial Tensile residual stresses at the surface are

    normally harmful sometimes leading to brittlefracture in fatigue

    Compressive residual stresses at the surfacenormally increase fatigue strength

    Residual stresses can be controlled in themanufacturing process

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    How Does It Work?

    Strain:

    L/L0 =d/d0

    Stress/Strain Relationships:

    ii = 1/E(ii)

    JJ = -/E(ii)

    ii = 1/E(ii) - /E(JJ + kk )

    Where L = length

    d = d-spacing = strain

    = stress

    = Poissons ratio

    E = Youngs modulus

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    Stress-Strain Equation for X-Ray

    Diffraction

    (33) = (d d0) / d0

    (33) = a3k a3lkl

    coscos sincos -sin

    aik = -sin cos 0

    cossin sinsin cos

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    Relative Axis

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    Stress-Strain Equation for X-Ray

    Diffraction

    (33) = (d d0) / d0 =

    11cos2sin2 + 12sin2sin

    2 +

    22sin2sin2 + 33cos2 +13cossin2 + 23sinsin2 =

    1/2S2(11cos2 + 12sin2 + 22sin

    2)sin2 +

    1/2S233cos2 + S1(11 + 22 + 33) +

    1/2S2(13cos + 23sin)sin2

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    Stress-Strain Equation for X-Ray

    Diffraction

    Assuming 33 = 13 = 23 =0

    (d d0) / d0 = 1/2S2(11cos2 + 12sin2 +

    22sin2)sin2 + S1(11 + 22)

    (d,=0 d0) / d0 = S1(11 + 22)

    (d d0) / d0 - (d,=0 d0) / d0 = (d d=0) / d0= 1/2S2sin

    2

    1/2S2 = (1+ )/E S1 = -/E

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    Measurement Direction

    Stress is a tensor

    and has magnitude

    and direction

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    Braggs Law Used To Measure

    Crystal Lattice Parameter, d

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    Effect of Tensile Stress on a

    Crystal Lattice Structure

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    Diffraction Pattern

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    Benefits of X-Ray Diffraction Residual

    Stress Analysis

    Can be nondestructive

    Gives a direct measure of strain and provides anquantitative value for stress

    Fast

    Accurate stress versus depth with electropolishing Repeatable

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    Benefits of X-Ray Diffraction Residual

    Stress Analysis

    Understand and quantify grinding burn to preventcomponent failure

    Analyze residual stress versus fatigue to aid incomponent life estimation

    Find cause of warping in machined components

    Analyze heat affected zones of weldments todetermine need for stress relief

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    References

    B. D. Cullity, Elements of X-ray Diffraction, Addison-Wesley,Reading, MA, 2nd Edition, 1977, pp. 447-477.

    Residual Stress Measurement by X-ray Diffraction SAE HS784,SAE, Warrendale, PA, 2003.

    Noyan and Cohen, Residual Stress Measurement by Diffractionand Interpretation, Springer-Verlag, New York, 1987.

    Metals Handbook, ASM, Metals Park, Ohio, 9th Ed. Vol. 10, 1986,pp. 380-392.

    SEM Residual Stress Seminar Notes, SEM, Bethel, CT. Northwestern University Residual Stress Course Notes, NU,

    Evanston, IL

    TEC Operation and Maintenance Manual, X-ray DiffractionSystems, Knoxville, TN.

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    Parting Thoughts

    Develop your talents Encourage, support and mentor your

    sisters Be active and contribute to your

    technical societies

    Get involved with VolSTEM or similarorganization

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    Parting Thoughts

    Know what you want dream big Believe in yourself Work (and play) hard Continue to learn and grow Dont let your education hold you back

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    Thank you!

    Questions?

    [email protected]

    865-218-5848

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    Comparison to Other Techniques

    Sectioning, Material Removal

    - gross residual stresses over large distance, depths- restricted to simple geometries

    Hole Drilling- uniform stress fields

    - complex geometries can be restrictive

    Barkhausen- limited to ferromagnetic materials

    - must have calibration standard

    Ultrasonics- requires calibration standard

    - sensitive to preferred orientation, grain size, second phases

    X-Ray Diffraction- more expensive than above techniques

    - surface technique

    - sensitive to large grain size and preferred orientation

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    Retained Austenite Analysis

    Nondestructive phase analysis of steels Can be performed in minutes Large, complex-shaped parts can be analyzed The only method for accurately measuring

    retained austenite in the 0% to 10% range

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    Retained Austenite Analysis

    Major phases in steel:

    -Austenite (FCC)-Ferrite (BCC) / Martensite (BCT)

    -Carbides

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    Retained Austenite Analysis

    By measuring and comparing intagrated intensities ofeach phase the amount of austenite can be calculated

    % + %M + %C = 100%

    Assuming no carbides gives:

    % = (IRM) / (IM R)

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    Retained Austenite Analysis

    Areas under diffraction peaks areproportional to amount of each phase

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    Retained Austenite Analysis

    8 < IM211 : IM200 < 11 (A)

    1.1 < I220 : I200 < 1.8 (B)

    1. If intensity ratios are outside (A) and (B) thenlarge grain size and/or preferred orientation are

    probable.2. If the intensity ratio is within (A) but higher than

    (B) then expect interference with 220. (If lower

    than (B) then expect interference with 200.)

    3.

    If the intensity ratio is within (B) but higher than(A) then expect interference with M211. (If lower

    than (A) then expect interference with M200.)

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    Retained Austenite Analysis

    Applications:Bearings - Dimensional stability

    - Preventing premature

    failures

    Large structures Dimensional stability

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    Retained Austenite Correction Flowchart

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    Production of X-rays

    Electronic transitions in an atom (schematic).

    Emission processes indicated by arrows.

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    Characteristic X-rays

    Spectrum of Mo at

    35kV. Line widthsare not to scale.

    Resolved Kdoublet is shown

    on an expanded

    wavelength scale

    at right.

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    X-ray Spectrum

    X-ray spectrum of molybdenum as a function of applied

    voltage. Line widths not to scale.

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    a0

    dl

    Crystallographic Planes

    h+k+l

    ad =

    0

    (for cubic only)

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    Comparison of the

    spectra of copperradiation before and

    after passage througha nickel filter. The

    dashed line is the

    mass absorptioncoefficient of nickel.

    Filters

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    Production/Properties of X-rays

    For x-ray diffraction, x-rays are produced inevacuated tubes by bombarding metallic targetswith electrons

    Two types of radiation- Bremstrahlung (slowing down of electrons)

    - Characteristic (electrons ejected from innershells of target material)

    Comparison with radiography

    X-ray absorption due to electron ejection from K,L, M shells

    I=I0e-t

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    Crystal Planes

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    X-Ray Diffraction Basics

    Braggs Law - N = 2dsin

    Penetration - t (infinite thickness) =3.45 sin

    (/)

    Fraction of scattered intensity from surface layer x: - Gx = [1-e-2x/sin]

    Back reflection region

    d = 0 =(-2dcos) + 2dsin or = (d/d) tan

    for a given strain (d/d), peak shift () is greater when 2 is larger

    Correction Factors: Lorentz PolarizationAbsorption

    BackgroundEtc.

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    Cold Work (Microstrain)

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    Measurement Pitfalls and Interpretation

    Theory predicts (assuming biaxial stresses) linear d-spacing

    versus sin plots

    Cause Diagnoses Solutions

    1. Large grain size 1. Move sample lateral

    and look for diffraction

    peak intensity changes

    1a. Use harder (more

    penetrating) radiaition

    1b. Use oscillation

    techniques

    1c. Use larger beam size

    1d. Use divergent beam

    2. Preferred orientation

    (texture)

    2. Intensity changes

    with -angle but

    not sample displacement

    2a. Use less sensitive

    reflections, i.e.,

    {h,0,0}, {h,h,h}

    2b. With PSPC systems,

    Oscillation techniques

    usually help

    2c. Analytical Methods

    A. Nonlinear d-spacing versus sin plots

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    Measurement Pitfalls and Interpretation (Cont.)

    Cause Diagnoses Solutions

    3. Surface Distortion 3. Broad diffraction peaks 3a. Use harder radiation

    3b. Electropolish

    B. Curved d-spacing versus sin plots

    Cause Diagnoses Solutions

    1. Stress Gradients 1. Curvature near=0 1a. Use harder radiation

    1b. Use Triaxial analysis

    techniques

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    Measurement Pitfalls and Interpretation(Cont.)

    C. Sin splits

    Cause Diagnoses Solutions

    1. Sample geometry 1. Split changes according to

    beam size

    1a. Use smaller beam

    1b. Mask sample

    2. misset 2. Rotate sample 180 to see

    if curve inverts

    2. Check sample

    diffractometer alignment

    3. Focusing circle effects 3. Rotate sample 180 to see

    if curve inverts

    3a. Use higher back

    reflection angle3b. Use only positive

    angles

    4. Sheer Stresses,

    Triaxial Stresses

    4. Rotate sample 180 to see

    if curve inverts

    4. Use analytical techniques

    to separate components of

    stress tensor