xray residual stress
TRANSCRIPT
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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?
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