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NASA TECHNICAL MEMORANDUM NASA TM X-71889 0- 00 (NASA-TM-X-71889j CORRELATIONS AMONG 7 OLTRASONIC PROPAG,.TIO· FACTORS AND FRACTORE >< TOOGHNESS PROPERTIES CF METALLIC MATERIALS (NASA) 31 P HC $4.CO CSCL 110 ex: G3j26 V'l ex: Z CORRELATIONS AMONG ULTRASONIC PROPAGATION FACTORS AND FRACTURE TOUGHNESS PROPERTIES OF METALLIC MATERIALS N76-21319 Unclas 21546 by Alex Vary Lewis Research Center Cleveland, Ohio 44135 REPROOUCED 8'1 NATIONAL TECHNICAL INFORMATION SERVICE u. S. DEPARTMENT OF COMMERCE SPRINGFIELD, VA. 22161 I TECHNICAL PAPER presented at Spring Conference of the Ameri an Society for Nondestructive Testing Los Angeles, California, March 8-11, 1976 https://ntrs.nasa.gov/search.jsp?R=19760014231 2020-08-05T04:32:16+00:00Z

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Page 1: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

NASA TECHNICALMEMORANDUM

NASA TM X-71889

0­00

~ (NASA-TM-X-71889j CORRELATIONS AMONG7 OLTRASONIC PROPAG,.TIO· FACTORS AND FRACTORE>< TOOGHNESS PROPERTIES CF METALLIC MATERIALS~ (NASA) 31 P HC $4.CO CSCL 110

ex: G3j26

V'lex:Z

CORRELATIONS AMONG ULTRASONIC PROPAGATION

FACTORS AND FRACTURE TOUGHNESS PROPERTIES

OF METALLIC MATERIALS

N76-21319

Unclas21546

by Alex Vary

Lewis Research Center

Cleveland, Ohio 44135

REPROOUCED 8'1

NATIONAL TECHNICALINFORMATION SERVICE

u. S. DEPARTMENT OF COMMERCESPRINGFIELD, VA. 22161

I

TECHNICAL PAPER presented atSpring Conference of the Ameri an Society

for Nondestructive Testing

Los Angeles, California, March 8-11, 1976

https://ntrs.nasa.gov/search.jsp?R=19760014231 2020-08-05T04:32:16+00:00Z

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. '

CORRELATIONS AMONG ULTRASONIC PROPAGATION,FACTORS AND

FRACTURE TOUGHNESS PROPERTIES OF METALLIC MATERIALS

by Alex Vary

. ;,'

.. :

Lewis Research Center

SUMMARY

"

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N"-'"00,"

, ,'" '

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,Empirical evidence is presented to shoW' the clos'e relation 'that''exists between, the ultr~sonic 'attenuation properties, and 'fracture, tough-,'n'ess (i.e., catastrophic crack propaga'tion) properties of p61,ycrystai­line metallic materials. Experimental evidence was obtained by 'ultra­sohiq111y probing specimens of two maraging steels' (a 200 and a 250grade) and a titanium alloy (Ti-8Mo-8V-2Fe-3Al). These specimens had

'been treated' to have a range of fracture toughness values fro~ 51 to'146 MPalffi. The specimens also exhibited a variety of yield strengths'and microstructures due to constitutive, cold working, and ,thermal agingdifferences.

,Relevant data were 'extracted by a frequency spectrum analysis proce­'dure 'over the frequency range'between 10 and 50 MHz. The effect ofmicrostructural factors on ultrasonic attenuation was evaluated in termsof· the slope of the attenuation coefficient versus frequency curve char­acteristic of each specimen material. It· was found. that the plane strain',fracture toughness, and also the yield strength of the materials examinedwe're -strongly related to the slope' of the attenuation versus frequencycU1;'ve.

,This paper gives an account of the methodology 'that was ,used to ex~

tract the required ultrasonic attenuation information .. Problems associ~

ated with'the methodology a~e discussed. Both theoretical speculationsand 'tentative experimental data are presented to indicate that plane'strain fracture toughness and yield strength can be properly correlatedthrough appropriate ultrasonic propagation factors. '

SYMBOLS

Units ,used' in the text are indicated when applicable. FUndamental. 'SI. , 'dimensions appear in parentheses .

A absorptiop. fact'o'r '(sm-l )

"'., .

. ," ..

", .'

:',"

.'•• 1"" '

ultrasonic' factor, ",',8etl

constant, '=,1" eq; (l~)

.....

": :..

.... "

:",

.',

.....

,,',

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B

Bl,B2

b

2

ratio of echo amplitudes relative to frequency

ultrasonic echo amplitude relative to frequency

constant, = 10-3 ~sl (cm MFa .1m), (N-1S ml/2 )

b' constant, eq. (13), l/lID, (m-l / 2)

c proportionality constant, eq. (7)

c' constant, eq. (13), (MPa) (cm) I~s, (N s -1 m-1)

D average grain diameter, (m)

d'

E

E'

f

m

n

R

t

v~

z

zc

-2constant, eq. (13), MPa, (N m )

-2Young's (elastic) modulus, (N m )

-2extensional (elastic) modulus, (N m )

-1frequency, MHz, (s )

-1critical "energy release factor," eq. (1), (N m )

critical stress intensity, MPalID, (N m-3/2)

-3/2plane strain fracture toughness, MPalffi, (N m )

-3/2conditional value of K1c ' MPalID, (N m )

exponent, eq. (7)

numerical factor

reflection coefficient

Rockwell-C hardness

scattering factor, (s 4 m-4)

(s 2 -2scattering factor, m )

specimen thickness, cm, (m)

-1longitudinal velocity, cm/~s, (m s )

-2 -1acoustic impedance of solid, = pv, (kg m s )

-2 -1acoustic impedance of couplant, (kg m s )

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3

attenuation coefficient, Np/cm, (m-l )

absorption attenuation coefficient, (m- l )

scatter attenuation coefficient, (m-l )

-1attenuation slope, = da/df, (s m )

attenuation slope at f-1

v/)., us/cm, (s m )

attenuation slope at-1

a = 1, us/cm, (s m )

(grain) boundary spacing, urn, (m)

wavelength, (m)

v

p

Poisson's ratio

3 -3density, g/cm , (kg m )

-2yield strength, MFa, (N m )

INTRODUCTION

The study described herein was made because there are strong in­centives for developing nondestructive ultrasonic methods for evaluatingmaterial fracture properties. First, less expensive a~ternatives wouldbe available to complement and corroborate mechanical destructive tests.Second, nondestructive techniques would be available for use on raw mate­rials or actual hardware to assess or verify mechanical properties.Third, from the standpoint of materials science, continued work of thistype should contribute to identification and analysis of factors thatcontrol toughness and thus aid in fracture control technology.

This work is a continuation of that described in reference 1. Theprevious work was a preliminary effort to establish the feasibility ofusing ultrasonic attenuation measurements to rank metals according totheir relative fracture toughness values. The purpose of the presentpaper is threefold. First, to describe the details and problems associ­ated with the acquisition and processing of ultrasonic data needed toevaluate attenuation characteristics. Second, to show that the result­ant attenuation measurements successfully correlate ultrasonic and crackpropagation properties of materials. Third, to indicate some tentativetheoretical grounds for the empirically observed relations between ultra­sonic and crack propagation factors.

The previously mentioned material is presented to encourage furtherstudies of the possible relations involved. Reasons for expecting ultra-

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R"8PRODUCIBILlTY OF THE\,marnA I. PAGE IS POOR

sonic measurements to correlate with fracture toughness properties aregiven in a background discussion. Relevant prior work is cited therein.Next, the approach and experimental procedures are explained. Finally,the results of this study are presented and discussed. Emphasis isplaced on the somewhat tentative nature of these results.

BACKGROUND

Fracture toughness is an intrinsic property that characterizes thefracture behavior of a material. It corresponds to a stress intensitywhich when a particular size crack is present will cause the crack topropagate catastrophically. Fracture toughness is expressed as a criti­cal stress intensity Kc ' It is related to the tensile modulus andcritical "strain energy release" factor Gc (refs. 2 and 3).

K = IE"'Gc c (1)

where E' equals E (Young's modulus) for plane stress and E!(l - v2)for plane strain conditions. The quantity Gc corresponds to the mate­rial's surface tension. It is a measure of the force required to extenda crack's perimeter by a unit length. This quantity has been related toyield strength cry (ref. 3).

Gc = ncr 0Y c(2)

where 0c iscoefficient.factors.

a critical crack opening displacement and n is a numericalThe coefficient n incorporates strain and associated

From the standpoint of ultrasonic assessment of Kc it is signifi­cant that E' in equation (1) is related to ultrasonic velocity v(ref. 4). It is known that Kc is related to a material's microstruc­ture. Because the attenuation of ultrasonic waves (e.g., elastic waves)is likewise related to microstructure, it follows that Kc is relatedto ultrasonic attenuation properties. Therefore, one should expect acorrelation between fracture toughness and ultrasonic propagation prop­erties via ultrasonic velocity and attenuation factors.

Acoustic emission studies have shown that ultrasonic stress wavesin metals are emitted by various disturbances; e.g., dislocation motions,microcracking, etc. (refs. 5 and 6). Moreover, acoustic emission studiesappear to support the expectation that in high toughness materials thepropagation and interaction of these ultrasonic stress waves are in­hibited by the attenuation properties of the material (ref. 7). There­fore, during rapid crack growth, the wave propagation properties of thematerial are probably significant. Ultrasonic attenuation measurementsmight then be expected to gauge factors that influence crack propagation

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and hence fracture toughness.

Some experimental support for the above-stated premise is available.By using shock stressing techniques, it can be shown that sustainedcrack growth occurs at times corresponding to the presence of a stresswave front at the crack tip. It appears that terminal crack speed isbounded by the stress wave's propagation velocity. Since crack speedsare less than wave velocities, stress wave reflections interact with andinfluence the growth of a running crack (ref. 8). Various investigatorshave studied the interaction and influence of ultrasonic waves on crackpropagation. For example, it has been shown that imposition of ultra­sonic waves will deflect a running crack in a predictable manner (ref. 9).Other studies have shown a close correspondence of brittle fracture andstress waves (refs. 10 and 11). It seems appropriate, therefore, to con­duct ultrasonic studies with a particular emphasis on what they can re­veal about interactions of spontaneous stress waves during fracture.

APPROACH

"Among the causeS of ultrasonic attenuation in polycrystallineaggregates is scattering by the microstructure and absorption due to dis­location dampening and elastic hysteresis. Ultrasonic attenuation can besummarized in terms of the attenuation coefficient a, the average graindiameter D, frequency f, and wavelength A (refs. 4 and 12). The totalattenuation coefficient is the sum of the absorption attenuation coeffi­cient, aa' and the scattering attenuation coefficient as:

for A> D (Rayleigh scattering domain),

(3)

as

(4)

and, for A < D (stochastic scattering domain) ,

as

and for the absorption domain,

(5)

Af (6)

where S and A are scattering and absorption factors, respectively.(The factor A may itself be a function of f over a sufficiently greatfrequency range.)

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For heterogeneous engineering materials, the a versus f depend­ence within a given frequency domain will involve some mixture of the ex­ponents given in the previous equations. It should, therefore, be ex­pected that microstructural variations will produce corresponding varia­tions in the slope of the a versus f curve (refs. 2 and 13). Accord­ingly, a general form of the attenuation versus frequency relation willbe taken as,

(7)

for the purposes of this study. Since the attenuation measurements inthis study were made within a limited frequency regime where equation (7)is applicable, m and c can be considered constants for a given mate­rial.

According to reference 1, a material's fracture toughness will varydirectly with B the slope of the attenuation versus frequency curvethat is characteristic of the material, where B = da/df evaluated at aparticular frequency. To find B, therefore, it is necessary to experi­mentally determine the equation relating a to f for each specimenmaterial.

The procedure used in this study was to ultrasonically probe aseries of specimens of materials for which fracture toughness values hadbeen measured. These measurements are conventionally made under condi­tions that give plane strain fracture toughness values KIc (ref. 14).The validity of fracture toughness measurements depend on the use ofappropriate test and specimen parameters. These vary with the materialbeing tested to ensure that plane strain conditions prevail. The quan­tity KIc thus implies a particular Kc value. The approach adoptedherein is to examine empirical correlations between KIc and S, whereB is evaluated at appropriate frequencies.

EXPERIMENTAL PROCEDURE

Specimen materials. - The materials used in this study were specimensof three different materials for which fracture toughness values werepreviously measured. There were five 200-grade maraging steel specimenseach aged at a different temperature to obtain a range of fracture tough­ness and yield strength values. A second set consisted of four specimenswith a 2S0-grade maraging steel composition. This second set was se­lected because the specimens spanned a wide difference in KIc valueswhile having virtually identical yield strengths. A third set of fourspecimens consisted of a titanium alloy with the compositionTi-8Mo-8V-2Fe-3Al. Each of these specimens was aged to have a differenttoughness and yield strength value.

Pertinent data on the three sets of specimens are given in table I.

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The data include plane strain fracture toughness, yield strength, andRockwell-C hardness values. The values of KIc cover the range from51 to 146 MFa';;;; while the yield strengths vary from 1075 to 1430 MFa.

Fracture toughness meaSurements quoted herein were made by personnelfrom the Lewis Research Center Fracture Branch, in conformance withplane strain criteria defined in ASTM E 399-70T, 4.2 (ref. 14), For twospecimens, the conditional value KQ defined in ASTM E 399-70T, 8.1(ref. 14) is given in place of KIc in table I. For these two speci­mens, only the conditional values were available. It can be assumedthat the KQ values are close to the actual KIc values but that theyrank lower in validity. In all cases yield strengths (at 0.2 percentelongation) were obtained by testing duplicates of the fracture toughnessspecimens. The Rockwell-C hardness values quoted in table I were takendirectly from the ultrasonic specimens described in the next section.

Ultrasonic specimens. - The original fracture toughness specimenswere sectioned, and a representative rectangular segment waS cut fromeach and ground to size. These segments were used as the ultrasonic testspecimens. This procedure ensured that the attenuation properties meas­ured were related specifically to objects that were actually subjects ofprevious fracture toughness tests. As indicated in figure 1, the ultra­sonic specimens were cut from near the fracture surface to further ensurethat they were representative.

A small segment of each ultrasonic specimen was reserved for metal­lographic examination. These were mounted and treated to exhibit theirmicrostructures, as shown in figure 2. The ultrasonic specimens hadsmooth ground surfaces (32 rms, approximately). The dimensions variedaccording to the material and the size of the original fracture toughnessspecimens from which they were sectioned. The thicknesses ranged from0.25 to 0.30 cm. The thicknesses were selected for compatibility withthe ultrasonic probe configuration and signal processing requirements.

The specimen thicknesses varied according to the material so thatthe time interval between successive echoes was approximately 2 micro­seconds. This corresponds to roughly one-third the delay time introducedby the fused quartz buffer attached to the transducer crystal (see fig. 3).Thus, at least three echo pulses from the specimen could be acquiredwithin the quartz delay line interval. This afforded a convenient meansof getting a clear set of strong signals for subsequent analysis.

Apparatus and procedure. - Ultrasonic velocity and attenuation meas­urements were made on the previously described ultrasonic specimens. Inmaking these measurements, the ultrasound was directed into the specimensalong an axis parallel to the fracture surface of the original fracturetoughness specimen. Thus, relative to the microstructure, the ultrasoundpropagated in the same direction as the crack did in the original KIctest (see fig. 1).

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The apparatus that waS used is indicated in figures 3 to 5. Theultrasonic measurements were made using piezoelectric crystal transducers.A cylindrical fused quartz buffer (delay line) was bonded to the trans­ducer crystal. Four broadband piezoelectric transducers were used. Eachcovered a separate nominal frequency. The transducer nominal (center)frequencies were 10, 20, 30, and 50 MHz. Being broadband the transducerfrequencies overlapped to cover the range from less than 10 to greaterthan 50 MHz. Glycerin was used as the couplant between the quartz bufferand the specimens.

The longitudinal ultrasonic velocity was measured for each specimenthrough the thickness. Velocity measurements were made at two center e­quencies - 10 and 30 MHz. Each specimen was also micrometrically meas­ured and weighed to determine density. From these measurements theacoustic impedance Z was determined and used to calculate the reflec­tion coefficient R for each specimen (ref. 15).

R = (Z - Z )!(Z + Z )c c(8)

The value for R thus obtained was used in a formula for calculating theattenuation coefficient a.

The above-mentioned velocity measurements were made by the "pulse­echo overlap" method (ref. 16). Because of the small specimen thicknesses,a modified version of the method waS used. This version involved threerather than the customary two, successive echoes. The first and secondechoes were encompassed in one gate while the second and third were en­compassed in a second gate as indicated in figure 4. The control oscil­lator frequency was then adjusted to bring all three echoes into coinci­dence (overlap). The period corresponding to the oscillator frequency isa measure of the time interval needed for sound to traverse twice thespecimen thickness t.

The formula used to calculate the attenuation coefficient a isbased on the frequency spectrum analysis method for measuring attenuation.This method is described in references 16 and 17. For the present case,the procedure was restricted to differential spectral analysis of onlythe first two echoes (Bl and B2) from the back (free) surface of thespecimens (see fig. 5). The method of spectrum analysis can also be usedto determine R by means of the ftont sur ace (FS) echo. Because Rwas accurately determined separately (by eq. (8)), it was unnecessary toinclude spectral analysis of the FS echo other than as a check. Theamplitude ratio of the echoes B (B2/Bl) was determine.d for a set offrequencies over the range between 10 and 50 MHz. These values for Bwere used with the measured values of R to compute a from (ref. 17)

a = tn(R/B)t2t (9 )

where t is the specimen thickness. The object of the differential spec-

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trum analysis is to generate a set of values of a versus f over asufficiently wide frequency range (in this case the range between 10 and50 MHz).

EXPERIMENTAL RESULTS

Reflection coefficient. - The measured ultrasonic propagation veloc­ities and material densities for the thirteen specimens are listed intable II. The longitudinal velocity was measured for each specimen attwo frequencies, 10 and 30 MHz. In all instances the 30 MHz velocity ex­ceeds the 10 MHz velocity. However, the difference is slight. It is ofthe order of 1 percent. This difference is ignorable in calculating thereflection coefficient R from equation (8). Even somewhat larger vari­ations in velocity would have virtually no effect on the value of R inthe present case. Therefore, R can be considered constant for the fre­quency regime involved.

Amplitude ratio characteristic. - A curve typical of the amplituderatio characteristic (ARC) of the thirteen ultrasonic specimens is pre­sented in figure 6. The ARC curve is a smooth curve based on a set ofraw B values that were determined for each of a set of frequencies inthe range between 10 and 50 MHz. The determination of the smooth ARCcurve is an important first step in the procedure for evaluating theattenuation coefficient a. The ARC curve constitutes the data fromwhich a is calculated for each frequency and is critical in determiningthe slope of the a versus f curve. There is no established theoreti­cal form for the ARC curve (ref. 12); therefore, this curve was deter­mined empirically by a graphical method as described hereinafter.

As is indicated in figure 6 the value of the reflection coefficientR is an upper bound on the ARC curve. The ARC can neither exceed norequal R, otherwise negative or zero attenuation coefficients wouldarise. Clearly, ~ must be a positive number.

Each data point in figure 6 represents the mean of several (usually10) raw B values. Generally, frequencies greater than 30 MHz yieldedfewer valid values because of low signal-to-noise ratios (at the tail endof the frequency spectra, see fig. S(b)). The mean B values arebracketed with error bars that represent the scatter in raw B values.

The scatter in raw data arose because of two factors. First, be­cause of the "noisiness" of the microstructures involved. This wasascribable to micro-defects, grain size and shape variations, and similarfactors. Second, because the amplitude ratios were obtained by repeatingmeasurements at various probe positions over the specimen. No two probepositions yielded exactly the same raw B value at a given frequency.Indeed, any particular set of B versus f values would tend to charac­terize local microstructural anomalies as well as the basic (smooth)microstructural properties. This poses a problem in attempting to get asmooth monotonic curve that represents the overall ARC.

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REPRODUCffiILITY OF THEOlUGHUd, PAGE IS POOlb

10

The procedure used to circumvent the above problem was to make "asufficient number of measurements. Thus, raw B measurements were madeuntil the mean values that were accumulated for a set of frequenciesappeared adequate to construct an ARC curve. This procedure furnisheda set of mean B values such as those represented in figure 6. Eachmean B value thus obtained is, of course, in error to some degree. Thefaired ARC curve constitutes a graphical estimation of the probablecoordinates of the true mean B values. This approach is recommendeduntil computerized signal averaging methods can be developed to amass thelarge amounts of data needed to firmly establish the true B versus f(ARC) curve.

Attenuation versus frequency curves. - Values for B were read fromthe ARC curves and substituted in equation (9) to compute values forthe attenuation coefficient a for each of a series of frequencies be­tween 10 and 50 MHz. A logarithmic plot of a versus f was made foreach specimen in the above-described manner.

It was found that each of the logarithmic plots tended to linearityand exhibited essentially fixed slopes above approximately 15 MHz. Forthe frequencies below about 15 MHz the plots deviated from linearity be­cause of geometric diffraction effects. However, only the linear por­tions of the a versus f plots are of interest. Therefore, a linear­ized curve based on frequencies of 15 MHz or greater was drawn for eachspecimen. An example of this is given in figure 7(a). Figure 7(a) alsoindicates the magnitude of the diffraction error at the low frequencies.This was confirmed by calculating diffraction correction factors for aset of frequencies from 10 to 20 MHz in accordance with reference 18.

Using a linear-regression least-squares method, an equation was de­termined for the line that best represented the logarithmic a versus fcurve of each ultrasonic specimen. This provided a set of values for cand m in equation (7). These parameters, c and m, are given intable II for each specimen.

Figures 7(b) through (d) show the attenuation versus frequency char­acteristic (AFC) curves for each of the specimens. Each material isgrouped according to type: 200-grade maraging steel in figure 7(b),250-grade maraging steel in figure 7(c), and titanium alloy in figure 7(d).These AFC curves are based on the c and m parameter values listedin table II.

The parameters c and m are taken herein to hold for all frequen­cies from 10 to over 50 MHz. This assumption is deemed appropriate as afirst approximation for the purpose of evaluating a at the higher fre­quencies. It is probable that the actual a versus f curve deviatesfrom linearity in the higher frequency region due to wavelength-to-grainsize ratio variations (see eq. (4) to (6)). Thus, the linear AFC curveparameters, c and m, probably tend to give e values that are too

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great at the extreme frequencies. However, the experimental method useddid not permit determining the exact relation of a to f at frequen­cies greater than approximately 50 ~mz. Herein, it is simply assumedthat the linear AFC curve can be meaningfully extrapolated to about640 MHz. This latter frequency is associated with wavelengths determinedin accordance with the grain boundary spacing dimension described next.

Metallography. - Figure 2 shows typical microstructures of each ofthe specimens. These photomicrographs were used for estimating the aver­age spacing of grain boundaries. The grain structure of the titaniumalloy is readily apparent, e.g., figure 2(h). Thus, the grain boundaryspacing of this material is easily measurable. For the 200-grade marag­ing steel specimens it is quite difficult to identify a grain structure,e.g., figure 2(a). However, it is possible to discern groups of parallellinear features in these specimens (i.e., twinning or subgrain boundaries).Since these features probably affect the transmission of ultrasonic wavesin the same manner as grain boundaries t they were used to determine anaverage "grain boundary" spacing for the maraging steels. Herein, anaverage (grain) boundary spacing waS taken as characteristic of each spec­imen. This average spacing dimension 0 was determined in accordancewith the ASTM intercept procedure described in reference 19. Measurementswere taken from both 100X and 250X photomicrographs such as those depictedin figure 2.

As explained hereinafter, the above-described estimate of (grain)boundary spacing 0 will determine a particular wavelength A (i.e., Awill be set equal to 0). This wavelength A determines the frequencyused in evaluating a. The spacing dimension 0 for each specimen isindicated in table II.

ANALYSIS OF RESULTS

Method of analysis. - The principal ultrasonic quantity used hereinto correlate ultrasonic with fracture toughness properties is a theslope of the AFC curve. The quantity a was evaluated in two ways:(a) relative to a "standard" attenuation, and (b) relative to a "critical"wavelength:

(a) First, noting that a = da/df and given equation (7) we have

m-la = cmf = am/f

Letting aal be the value of a evaluated at the frequency where(l = 1, i.e., at unit C'standard") attenuation, then

11m::::: me

(10)

(11)

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(b) The second method of evaluating a involves the selection of aparticular frequency for substitution in equation (10). This particularvalue for f is taken as that associated wi th a "critical" or resonancewavelength, here taken equal to the (grain) boundary spacing dimension6. The corresponding value of a is labeled a6'

Analysis of the results of this study indicated that the productvia6 correlates strongly with the quantity Kic/cry. It was also foundthat the quantity anI correlates strongly with KIc' The values foranI, a6, and via6 were determined for each specimen and are listed intable II.

The aql factor. - Figure 8 is a plot of anI versuS KIc for allthe specimens. Inspection of figure 8 shows that the data can be groupedaccording to yield strength. For example, the four data points for the250-grade maraging steel specimens fallon the same line. These fourspecimens have virtually identical yield strengths. Also, two pairs of200 grade maraging steel and one pair of titanium alloy specimens hadlike yield strengths (within 10 MPa). These data pairs can be connectedwith straight lines that parallel that for the 250 grade maraging steel.The pattern that emerges is indicated by the sets of parallel lines drawnthrough the data for the various specimen materials. Each line is labeledwith the (approximate) yield strength shared by the data points it in­cludes. The anI versus KIc plot for each material (fig. 8) thus ap­pears to consist of a set of lines that are isometric with respect to cry.

(12)

where a is a function oflxlO-3 us/ (cmMPaliii). (Notea common slope of unity.)

cry and b is a conversion factor equal tothat the lines in fig. 8 all apparently share

The information in figure 8 can be developed further. Assuming thatthe above linear isometric grouping is correct, an equation can be deter­mined for each line. This gives a set of values for a in equation (12)for specimens sharing the same yield strength, where a = anI - bKIc'Accordingly, figure 9(a) is a plot of yield strength cry versus a(herein termed the "ultrasonic factor") for the two materials for whichthere are sufficient data to make this plot: the 200-grade maragingsteel and the titanium alloy. It is apparent from this plot that thedata for these two materials produce linear correlations between yieldstrength and the ultrasonic factor a.

It is instructive to compare figure 9(a) with figure 9(b) which is aconventional plot of yield strength versus fracture toughness cry versusKIc for these two materials. This plot indicates the general trend ofdecreasing yield strength with increasing fracture toughness. Alsoapparent is the considerable deviation from this general trend. Compari­son of the two figures, 9(a) and (b), indicates that ultrasonic factorscan be used to better establish the relation between cry and KIc'

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13

Obviously, introduction of the ultrasonic factor a brings more coher­ence to the relation between KIc and Oy. Figure 9(a) thus suggeststhe following general relation.

a'o + b'K + c'S = d'Y Ic al

where, based on figure 9(a), the equation for the 200-grade maragingsteel is

(13)

and the equation for the titanium alloy is

(13a)

(13b)

It should be noted that Sal was evaluated at frequencies where the AFCcurve was most valid; i.e., required either little or no extrapolation.

The viSe factor. - Figure 10 is a plot of viSe versus Kic/oyfor all the specimens tested. A linear regression curve fit wasmade for the data shown in figure 10. The goodness-of-fit is 0.99 forthe curve of figure 10. This curve has the equation

(14)

(IS)

Thus the quantity K1c/Oy apparently varies nearly as the cube root ofViSe. However, the AFC curves probably give too high values for Se(as was mentioned previously relative to fig. 7). Therefore, the actualexponent on ViSe in equation (IS) is probably greater than that which sindicated by the current data.

DISCUSSION

Interpretations. - The foregoing relations illustrate that fracturetoughness, yield strength and, by implication, associated material prop­erties, are intimately connected with ultrasonic propagation properties.It appears, for example, that KIc and cry can be properly correlatedwith each other via material factors such as those related to the quan­tity Sal' see figure 9(a).

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REPRODUCIDILITY OF THEORIGINAL PAGE IS POOR

14

A possible theoretical basis for the observed relations can bededuced from the concepts introduced in the BACKGROUND section of thisreport. Briefly, one can postulate that the physical processes involvedin crack propagation depend on the propagation and interactions of stresswaves.

It might be noted that there is nothing extraordinary in the propo­sition that stress or sound waves promote cracking ahead of the crackfront. One need only recall that concentrated sound of the proper pitchcan shatter a highly stressed solid (e.g., a crystal goblet). Moreover,the process need not involve contiguous regions. It probably involvesmicro fractures and crack nucleations at a distance from the main crackfront. In this context, it seems that the previously stated premise andempirical results prove to be complementary.

An alternative explanation of the empirical correlations can bebased on ultrasonic attenuation as a measure of the distribution densityof sub granular scattering centers or dislocations. Ultimately, Kc , Oy,and S are, of course, determined by the number and mobility of disloca­tions (refs. 3 and 6). Therefore, it can be argued that the empiricalcorrelations testify that the ultrasonic factors Sal and So simplymeasure dislocation densities or loop lengths. In this case absorptionattenuation would tend to predominate, and the a verSUS f curves infigures 7(b) through (e) should all have slopes near unity, according toequation (6). The data in table II show that the a versus f slopes(the m values) are predominantly 2 or greater (at least in the fre­quency domain of the actual measurements). It is probable that some mix­ture of absorption and Rayleigh and stochastic scattering was involvedwithin the frequency domain where a was determined. Regardless of theexact mode of ultrasonic wave energy dissipation, I believe that theresults herein suggest that the factors Sal and v~So are indirectmeasures of stress wave energy losses during crack growth.

With reference to figure 10, both the quantities v~So and KYc/0yare related to energy. The latter has the dimensions of specific energy(i.e., energy per unit area). If the dimensionless quantity v~So is ameasure of energy loss by stress wave attenuation, it is not surprisingthat v~So and KYc/0y correlate well irrespective of the materials in­volved. It is surprising, though, that the strong correlation seen infigure 10 was obtained despite the approximations and extrapolations madein evaluating So. For example, So was somewhat crudely evaluated. Toevaluate So it was assumed that the equations for attenuation curves inthe frequency range from 10 to 50 MHz applied over the extended frequencydomain (up to 640 MHz) associated with crack extension stress waves.This extrapolation was needed to overcome the frequency limitation of theultrasonic equipment used. It appears, therefore, that ultrasonic prob­ing in this lower frequency domain gives a measure that is proportionalto the energy that is potentially transferable to crack extension involv­ing the higher frequency stress waves.

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15

Equation 13, which is based on figures 8 and 9, is interest ng fromthe standpoint of an implied energy partition among the various terms:KIc ' Oy, and Bal' The terms in equation (13) ate probably related to anenergy partition among plastic deformation, crack nucleations, and stresswave interactions. Based on the limited results of this study, it appearsthat the coefficient of KIc or b' in equation (13) will be positive ornegative depending on the mode of fracture. If it is predominantly duc­tile as in the 200 grade maraging steel (fig. ll(a)), then b' is posi­tive, as in equation (13a). If brittle fracture predominates as in thetitanium alloy (fig. ll(b)), then b' is negative, as in equation (13b).The sign of c' is opposite that of b'. Apparently this depends uponwhether the crack nucleation sites are energy sources or sinks duringfracture.

The data reported thus far is, of course, inadequate to confirm theabove speculations. More work is needed to establish the attenuationproperties of a wider range of materials for which fracture toughnessdata can be obtained. In particular, advanced electronic signal process­ing and computer processing methods will be essential to amass and ana­lyze the ultrasonic signals involved over a considerably greater frequencydomain. In situ signal averaging procedures will be needed to reduce theinherent scatter and grain noise effects that attend acquisition of theraw B (amplitude ratio) data.

Applications. - Given empirical relations such as those in equa­tions (13a) , (13b) , and (14), nondestructive ultrasonic measurements canapparently be used to determine fracture toughness and yield strengthvalues. This could be done by simultaneous solution of pairs of equa­tions, such as equations (13a) and (14), if the quantities Bal andv~B6 are known. Of course, other data are needed to evaluate thelatter quantities. It would be necessary to identify the material andits grain boundary spacing dimension 6. Conceivably, further refine­ment of ultrasonic methods can produce this additional information (e.g.,through relations such as those in eqs. (4) and (5), see tef. 12).

It is reasonable to conclude that once having established appropri­ate parameters for a material, ultrasonic methods can be used to compilefracture toughness data for subsequent specimens of a given material.This could be accomplished with specimens that are considerably smallerthan conventional fracture toughness specimens. These ultrasonic speci­mens would have to meet certain specifications. As a minimum, they shouldbe dimensioned in accordance with the ultrasonic probe requirements toensure adequate signal recovery. This type of requirement may pose dif­ficult problems in attempts to adopt the technique to some actual hardwareitems. However, it is possible to foresee computer-assisted transducersthat can adapt the technique to field applications.

Perhaps the most significant implications of the correlations re­ported herein are concerned with analysis of fracture micrornechanics and

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16

hence with fracture control technology. It appears that nondestructiveultrasonic measurements can be an important adjuct to mechanical destruc­tive testing. For example, the interpretation of the relations betweenKIc and cry are clarified by the additional data provided by the ultra­sonic factors Sal and v~So ' as in figures 8 to 10.

SUMMARY OF RESULTS

The results presented herein indicate a close relation between rapidcrack extension and ultrasonic (stress) wave propagation phenomena inmetallic materials (two grades of maraging steel and a titanium alloy).The correlations were obtained by ultrasonically probing specimens ofthese materials for which fracture toughness and yield strength werepreviously measured.

Two major empirical relations between ultrasonic and crack (fracture)toughness factors are developed in this report. The first of these in­volves the plane strain fracture toughness value KIc and the ultrasonicattenuation factor Sal' The quantity Sal is the slope of the attenua­tion coefficient a versus frequency f curve (i.e., S = da/df) evalu­ated at the frequency where a equals unity. The second correlation in­volves the specific energy term Klc/cry and the ultrasonic factor v~So'The quantity So is the slope of the a versus f curve evaluated atthe frequency corresponding to a particular wavelength. This wavelengthis determined by a spacing dimension 0 that is characteristic of thematerial's microstructure, i.e., grain boundary spacing. The quantityv~ is longitudinal velocity of the ultrasound and cry is the material'syield strength. Strong correlations were found for Sal versus KIcand for v~So versus Ktc/cry for the four materials studied.

The results indicate that the v~So versus Klc/crythe specimen materials evaluated can be represented by ahaving the general form.

data for allsingle curve

The relation between Sal and K1c is more complex since it in­volves a family of curves that are isometric with respect to cry. Fortwo of the specimen materials sufficient data were available to obtainrelations among KIc' cry, and Sal' Thus, for the 200 grade maragingsteel and the titanium alloy these relations had the general form

a'cr + b'K + c'S = d'Y Ic al

In this latter relation the algebraic signs of b'and apparently determined by the dominant fracturetile) .

and c' are oppositemode (brittle or duc-

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18

7. Yosio Nakamura, C. L. Veach, and B. O. McCauley, "Amplitude D stributionof Acoustic Emission Signals," Acoustic Emission, ASTM STP-505, 1972,pp. 164-186, American Society for Testing and Materials, Philadelphia.

8. H. Kolsky and D. Rader, "Stress Waves and Fracture," Fracture - AnAdvanced Treatise, Ch. 9, Harold Liebowitz, ed., vol. I, 1971, pp.533-567, Academic Press, New York.

9. F. Kerkhof, "Wave Fractographic Investigations of Brittle FractureDynamics," Proceedings of an International Conference on DynamicCrack Propagation, George C. Sih, ed., 1973, pp. 3-35, NoordhoffInternational Publ., Leyden, The Netherlands.

10. H. Kolsky, "Recent Work on the Relations Between Stress Pulses andFracture," Proceedings of an International Conference on Dynamic CrackPropagation, George C. Sih, ed., 1973, pp. 399-414, Noordhoff Interna­tional Publ., Leyden, The Netherlands.

11. H. C. vanElst, "The Relation between Increase in Crack Arrest Tempera­ture and Decrease of Stress Wave Attenuation by Material Embrittle­ment," Proceedings of an International Conference on Dynamic CrackPropagation, George C. Sih, ed., 1973, pp. 283-320, Noordhoff Inter­national Publ., Leyden, The Netherlands.

12. Emmanuel P. Papadakis, "Ultrasonic Attenuation Caused by Scattering inPolycrystalline Metals," Journal of the Acoustical Society of America,Vol. 37, Apr. 1965, pp. 711-717.

13. R. L. Roderick and R. Truell, "The Measurement of Ultrasonic Attenuationin Solids by the Pulse of Technique and Some Results in Steel," Journalof Applied Physics, Vol. 23, Feb. 1952, pp. 267-279.

14. W. F. Brown, Jr., ed., Review of Developments in Plane Strain FractureToughness Testing, ASTM STP-463, 1970, American Society for Testingand Materials, Philadelphia.

15. J. Krautkramer and H. Krautkramer (B. W. Zenzinger, trans.), UltrasonicTesting of Materials, 1969, pp. 21-22; 91-100, Springer-Verlag, NewYOTk.

16. E. P. Papadakis, "The Measurement of Small Changes in Ultrasonic Velocityand Attenuation," Crit cal Reviews in Solid Stare Sciences, Vol. 4,Aug. 1973, pp. 373-418.

17. L. C. Lynnworth, "Attenuation and Reflection Coefficient Nonogram,"Ultrasonics, Vol. 12, 1974, pp. 72-73.

18. Emmanuel P. Papadakis, "Ultrasonic Diffraction Loss and Phase Change inAnisotropic Materials," Journal of the Acoustical Society of America,Vol. 40, Oct. 1966, pp. 863-874.

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19

19. 1973 Annual Book of ASTM Standards, Part 31, 1973, p. 422, AmericanSociety for Testing and Materials, Philadelphia.

TABLE 1. - CHARACTERISTICS OF SPECIMEN MATERIALS

Specimen Aging Hardness Yield Fracture Energytemperature, Rockwell, strength,d toughness,e parameter,

K Rc Oy, KIc ' Kic/Oy,MPa MPaliil MJ/m2

al-200 700 39.9 1320 (113) 9.67a2-200 728 42.9 1430 98.1 6.73a3-200 756 43.2 1430 92.3 5.96a4-200 783 42.8 1330 103 7.98a5-200 811 40.9 1210 (110) 9.98bl-250 672 45.7 1400 118 9.94b2-250 672 45.7 1400 117 9.77b3-250 838 46.1 1400 139 13.8b4-250 838 46.1 1400 146 15.2cl-Ti 700 37.5 1075 53.7 2.6Bc2-Ti 756 43.4 1370 51.0 1. 90c3-Ti 811 41.1 1230 59.9 2.92c4-Ti 867 38.0 1085 70.0 4.52

a200 grade maraging steel, cold rolled 50 percent, and aged for8 hours.

b250 grade maraging steel, annealed at 1090 K, air cooled, and agedfor 6 hours.

CTitanium alloy (Ti-8Mo-8V-2Fe-3A1 composition), solution heattreated at 1144 K for 1 hour, water quenched, and aged 8 hours.

dYield strength measured at 0.2 percent elongation (to convert to ksi,divide by 6.89).

eplane strain, conditional KQ values in parentheses (to convert toksifG1., divide by 1.10).

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ULl1lASONIC SPECIMEN DIMENSIONS,

200 GRADE MARAGING STEEL, d • 1.55 CM, h • 1.95 CM, t· 0,25 CM,250 GRADE MARAGING STEEL, d • 2,00 CM, h • 2,55 CM, t· 0,25 CM,TITANIUM ALLOY, d· 2,55 CM, h· J, 15 CM, I· 0, 3D CM,

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Figure 1. - Typical excision of ultrasonic specimen from fracturetoughness specimen.

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Page 27: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

4.0

3.0

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h ,~AFC CURVE COMPU7EO BY.3 I LINEAR REGRESSION

l-I \

'-ORIGINAL CURVE UNCORRECTEDfOR DiffRACTION EffEC7S

.1 ~-----;!;;----'--+,_L-+,-...l..co!:--L..j,10 20 50 60 10 20 40

fREQUENCY, f, MHz

(.1 TYPICAL AfC CURVE AND ORIGINAL CURVE 10omOI Ibl AfC CURVES fOR 200 GRADE MARAGING STEEL SPEC-INDICATING MAGNITUOE Of DiffRACTION EffECT. IMENS.

Figure 7. - Attenuation coefficient vs. frequency characteristic lAFC) curves.

Page 28: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

10

Figure 7. - Conc.luded.

10 40 SO 60 10FREQUENCY. f, MHz

Icl AFC CURVES FOR 150 GRADE MARAGING STEEL ~I AFC CURVES FOR TITANIUM ALLOY SPECIMENS.SPECIMENS.

. 1'---__--I..lJLL---.J'------'-_-'-.l-.l-Ll-..Jto

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Page 29: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

Oy' 1400 MP,

60 80 100 110FRACTURE roUGHNESS. K1C ' MP, jii

figure 8. - Ultrasonic attenuation faclor ~(I1 as a function of fracture toughness K1C and yieldstrength Oy.

o

1400 TITANIUM ALLOY m-ll\lo-8V-2Fe-lAll0 100 GRADE MARAGING STEEL0 2SO GRADE MARAGING STEEl

110

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Page 30: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

o TI-Bh\o-SV-2Fe-lAlo 200 GRADE MARAGING STEEl

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ULTRASONIC fACTOR. aX103, lis/em fRACTURE TOUGHNESS, Kle , MPavrnloll YIElD STRENGTH AS A fUNCnON Of (bl CONVENTIONAL PLOT Of YIELD

HE ULTRASONIC fACTOR a a ~al - STRENGTH AS A fUNCTION OFbK IC ' II· IIs/cm MPao/riil. FRACTURE TOUGHNESS.

Figure 9. - Correlation 01 yield strength kl fracture toughness for a titanium alloy anda marill}lng steel.

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fRACruRE TOUGHNESS FACTOR,K~e foy. MJfm2

Flgure 10. • Correlation of ultraso91c attenuation factlr ¥{~6and fracturl! tooghness factor Kle'oy •

Page 31: NASA TM X-71889€¦ · nasa technical memorandum nasa tm x-71889 0 00 ~ (nasa-tm-x-71889j correlations among 7 oltrasonic propag,.tio· factors and fractore >< tooghness properties

REPRODUCIBILITY OF THBORIGINAl. PAGE IS POOR

tal fRACTOGRAPH Of;:OO GR{l,O£MARA.GING STEEl, SPECIMEN 1-;:00, tyPI·CAllNDrCATION OF DUCTILE FRACTURE.

ibl FRACTDGRAPH OF T1T"-NIUM ALLOY. SPECIMEN 3-H, TYP\CAlINOICATIDNOF BRmlE FRACTURE.

figure II. - Scanning electron micrographs ollraclure surfaces typical oftoo grade rraraging steel and titanium specimens. Original magnificationwaS XIOO. Am:"" indicates direction of (rack e.-tension .

.::30