Fracture Toughness
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Fracture Toughness

In materials science, fracture toughness is a property which describes the ability of a material to resist fracture, and is one of the most important properties of any material for many design applications. The linear-elastic fracture toughness of a material is determined from the stress intensity factor () at which a thin crack in the material begins to grow. It is denoted KIc and has the units of or . Plastic-elastic fracture toughness is denoted by JIc, with the unit of J/cm2 or lbf-in/in2, and is a measurement of the energy required to grow a thin crack.

The subscript I denotes mode I crack opening under a normal tensile stress perpendicular to the crack, since the material can be made deep enough to stand shear (mode II) or tear (mode III).

Fracture toughness is a quantitative way of expressing a material's resistance to brittle fracture when a crack is present. A material with high fracture toughness may undergo ductile fracture as opposed to brittle fracture. Brittle fracture is characteristic of materials with low fracture toughness.[1]

Fracture mechanics, which leads to the concept of fracture toughness, was broadly based on the work of A. A. Griffith who, among other things, studied the behavior of cracks in brittle materials.

A related concept is the work of fracture () which is directly proportional to , where is the Young's modulus of the material.[2] Note that, in SI units, is given in J/m2.

Fracture toughness and materials class

Fracture toughness vs. Yield strength

Just as the elastic properties of materials, like elastic moduli and strength, vary among material class, so too does the fracture toughness. Figure 1 graphs the fracture toughness vs. strength for various materials and materials classes.[3] However, unlike most elastic properties, fracture toughness displays a wide variation across materials, about 4 orders of magnitude. As can be expected, metals hold the highest values of fracture toughness. Since cracks cannot easily propagate in tough materials, this makes metals highly resistant to cracking under stress and gives their stress-strain curve a large zone of plastic flow. Comparatively, engineering ceramics have a lower fracture toughness, which leads to ease of cracking, but show an exceptional improvement in the stress fracture that is attributed to their 1.5 orders of magnitude strength increase, relative to metals. Of note is the fracture toughness of composites (made by combining engineering ceramics with engineering polymers) (in the zone of engineering alloys), which greatly exceeds the individual fracture toughness of the constituent materials.

Within material groups (classes) there is a further subdivision that depends on the relation between strength and toughness between different material subgroups. The ovals, or "balloons" within each material class tend to have a sloping trend that describes the subgroup's strength-toughness relationship. For example, take the alloy system's downward sloping trend. This relationship indicates, that within an alloy class an increase in strength leads to a decrease in fracture toughness regardless of the strengthening mechanism used. For this reason, it is beneficial to think of an increase in strength (within the engineering alloys) as a direct decrease in fracture toughness, which is correlated with a lower ductility of the material. This, however, is not the trend for other material classes. As a first example, consider the polymer foams and porous ceramics. In direct contrast to alloys, the trend in this material class is to have an upward slope. Explicitly, when the strength of these materials is increased we can expect to see an accompanied increase in fracture Yitoughness. Indeed, in the subgroup of balsa and ash we observe a close to one order of magnitude increase in both properties. Porous ceramics have been shown to behave exactly like this under both compression stress and tensile stress, however, the fracture toughness values are ten times lower under tension. This behavior can most easily be grasped by considering the porosity of these materials, where these voids can be modeled as preexisting cracks, which increase the nucleation energy of cracks under stress and impede the propagation of these cracks. Note that the engineering ceramics also show the same sloping trend as the porous ceramics, however, the slope is much greater, which makes it less noticeable in the log-scale.

In general, materials that are on the upper-leftmost part of the diagram are used to design a system's failure against flow, because these materials yield before they are fractured. While materials on the lower rightmost part of the diagram are used to design a system's failure against fracture, because these materials fracture before yielding.

Example values

The following table shows some typical values of fracture toughness for various materials:

Material type Material KIc (MPa · m1/2)
Metal Aluminum 14-28
Aluminum alloy (7075) 20-35[4]
Inconel 718 73-87[5]
Maraging steel (200 Grade) 175
Steel alloy (4340) 50
Titanium alloy 84-107[6]
Ceramic Aluminum oxide 3-5
Silicon carbide 3-5
Soda-lime glass 0.7-0.8
Concrete 0.2-1.4
Polymer Polymethyl methacrylate 0.7-1.60
Polystyrene 0.7-1.1
Composite Mullite-fibre composite 1.8-3.3[7]
Silica aerogels 0.0008-0.0048[8]

Stability of crack growth

Consider a body with flaws (cracks) that is subject to a load; the stability of the crack can be assessed as follows. We can assume for simplicity that the loading is of constant displacement or displacement controlled type (such as loading with a screw jack); we can also simplify the discussion by characterizing the crack by its area, A. If we consider an adjacent state of the body as being one with a broader crack (area A+dA), we can then assess strain energy in the two states and evaluate strain energy release rate.

The rate is reckoned with respect to the change in crack area, so if we use U for strain energy, the strain energy release rate is numerically dU/dA. It may be noted that for a body loaded in constant displacement mode, the displacement is applied and the force level is dictated by stiffness (or compliance) of the body. If the crack grows in size, the stiffness decreases, so the force level will decrease. This decrease in force level under the same displacement (strain) level indicates that the elastic strain energy stored in the body is decreasing--is being released. Hence the term strain energy release rate which is usually denoted with symbol G.

The strain energy release rate is higher for higher loads and broader cracks. If the strain energy so released exceeds a critical value Gc, then the crack will grow spontaneously. For brittle materials, Gc can be equated to the surface energy of the (two) new crack surfaces; in other words, in brittle materials, a crack will grow spontaneously if the strain energy released is equal to or more than the energy required to grow the crack surface(s). The stability condition can be written as

elastic energy released = surface energy created.

If the elastic energy released is less than the critical value, then the crack will not grow; equality signifies neutral stability and if the strain energy release rate exceeds the critical value, the crack will start growing in an unstable manner. For ductile materials, energy associated with plastic deformation has to be taken into account. When there is plastic deformation at the crack tip (as occurs most often in metals) the energy to propagate the crack may increase by several orders of magnitude as the work related to plastic deformation may be much larger than the surface energy. In such cases, the stability criterion has to be restated as

elastic energy released = surface energy + plastic deformation energy.

The problem can also be formulated in terms of stress instead of energy, leading to the terms stress intensity factor K (or KI for mode I) and critical stress intensity factor Kc (and KIc). These Kc and KIc (etc.) quantities are commonly referred to as fracture toughness, though it is equivalent to use Gc. Typical values for KIcare 150 MN/m3/2 for ductile (very tough) metals, 25 for brittle ones and 1-10 for glasses and brittle polymers. Notice the different units used by GIc and KIc. Engineers tend to use the latter as an indication of toughness.

Conjoint action

There are a number of instances where this picture of a critical crack is modified by corrosion. Thus, fretting corrosion occurs when a corrosive medium is present at the interface between two rubbing surfaces. Fretting (in the absence of corrosion) results from the disruption of very small areas that bond and break as the surfaces undergo friction, often under vibrating conditions. The bonding contact areas deform under the localised pressure and the two surfaces gradually wear away. Fracture mechanics dictates that each minute localised fracture has to satisfy the general rule that the elastic energy released as the bond fractures has to exceed the work done in plastically deforming it and in creating the (very tiny) fracture surfaces. This process is enhanced when corrosion is present, not least because the corrosion products act as an abrasive between the rubbing surfaces.

Fatigue is another instance where cyclical stressing, this time of a bulk lump of metal, causes small flaws to develop. Ultimately one such flaw exceeds the critical condition and fracture propagates across the whole structure. The fatigue life of a component is the time it takes for criticality to be reached, for a given regime of cyclical stress. Corrosion fatigue is what happens when a cyclically stressed structure is subjected to a corrosive environment at the same time. This not only serves to initiate surface cracks but (see below) actually modifies the crack growth process. As a result, the fatigue life is shortened, often considerably.

Stress-corrosion cracking (SCC)

This phenomenon is the unexpected sudden failure of normally ductile metals subjected to a constant tensile stress in a corrosive environment. Certain austenitic stainless steels and aluminium alloys crack in the presence of chlorides, mild steel cracks in the presence of alkali (boiler cracking) and copper alloys crack in ammoniacal solutions (season cracking). Worse still, high-tensile structural steels crack in an unexpectedly brittle manner in a whole variety of aqueous environments, especially chloride. With the possible exception of the latter, which is a special example of hydrogen cracking, all the others display the phenomenon of subcritical crack growth; i.e. small surface flaws propagate (usually smoothly) under conditions where fracture mechanics predicts that failure should not occur. That is, in the presence of a corrodent, cracks develop and propagate well below KIc. In fact, the subcritical value of the stress intensity, designated as KIscc, may be less than 1% of KIc, as the following table shows:

Alloy KIc () SCC environment KIscc ()
13Cr steel 60 3% NaCl 12
18Cr-8Ni 200 42% MgCl2 10
Cu-30Zn 200 NH4OH, pH7 1
Al-3Mg-7Zn 25 aqueous halides 5
Ti-6Al-4V 60 0.6M KCl 20

The subcritical nature of propagation may be attributed to the chemical energy released as the crack propagates. That is,

elastic energy released + chemical energy = surface energy + deformation energy.

The crack initiates at KIscc and thereafter propagates at a rate governed by the slowest process, which most of the time is the rate at which corrosive ions can diffuse to the crack tip. As the crack advances so K rises (because crack size appears in the calculation of stress intensity). Finally it reaches KIc, whereupon swift fracture ensues and the component fails. One of the practical difficulties with SCC is its unexpected nature. Stainless steels, for example, are employed because under most conditions they are passive; i.e. effectively inert. Very often one finds a single crack has propagated whiles the left metal surface stays apparently unaffected.

Toughening mechanisms

Intrinsic mechanisms

Intrinsic toughening mechanisms are processes which act ahead of the crack tip to increase the material's toughness. These will tend to be related to the structure and bonding of the base material, as well as microstructural features and additives to it. Examples of mechanisms include crack deflection by secondary phases, crack bifurcation due to fine grain structure and modification to the grain boundaries, and crack meandering by pores in the material. Any alteration to the base material which increases its ductility can also be thought of as intrinsic toughening.[9]

Extrinsic mechanisms

Extrinsic toughening mechanisms are processes which act behind the crack tip to resist its further opening. Examples include fibre/lamella bridging, where these structures hold the two fracture surfaces together after the crack has propagated through the matrix, crack wedging from the friction between two rough fracture surfaces, microcracking, where smaller cracks form in the material around the main crack, relieving the stress at the crack tip by effectively increasing the material's compliance, and transformation toughening.[10]

"Transformation toughening" is a phenomenon whereby a material undergoes one or more martensitic (displacive, diffusionless) phase transformations which result in an almost instantaneous change in volume of that material. This transformation is triggered by a change in the stress state of the material, such as an increase in tensile stress, and acts in opposition to the applied stress. Thus when the material is locally put under tension, for example at the tip of a growing crack, it can undergo a phase transformation which increases its volume, lowering the local tensile stress and hindering the crack's progression through the material. This mechanism is exploited to increase the toughness of ceramic materials, most notably in Yttria-stabilized zirconia for applications such as ceramic knives and thermal barrier coatings on jet engine turbine blades.[11]

This martensitic transformation occurs as a result of stress and parallels elastic transformation, it is also quite similar to the transformation that occurs within TRIP steels, but that martensitic transformation is a result of plastic strain. The two phases that exist within pure Zirconia are the tetragonal form at high temperature, and the monoclinic form at low temperature. The transformation in pure Zirconia contains significant shear (ca. 7%) and dilatational strains (ca. 4%). Thermal cracking and even loss of key structural principles can result from these strains if cooling occurs rapidly. Additionally, cooling induces this transformation sluggishly as only a small fraction of the tetragonal form actually transforms. For specific PSZ compositions, the transformation transition temperature falls below room temperature with stress assistance. Figure 1 illustrates the transformation induced via a crack and its corresponding stress field. If tetragonal particles lie within one radius (rc) of the crack fracture plane, certain particles transform into the monoclinic phase, and the material toughness increases as a result of the work invested into the transformation process.[12]

Visual representation of transformation toughened pure Zirconia. The crack induces a stress intensification that results in the transformation of some tetragonal particles into monoclinic phase particles that lie within the one rc zone.

The toughness contributed from transformation toughness is quite analogous to that from crack toughening, and the equations involved will be quite similar. Key parameters include the stress, which induces the transformation, the transformational strain, and the composition within one rc of the crack. This distance is dependent upon the fracture toughness of the matrix along with the inducing stress. Furthermore, the phenomena within transformation toughening also parallel those within microcrack toughening. The grain-size effect of microcrack toughness is quite analogous to the particle-size effect prevalent within transformation toughening. This causes the stress required to initiate martensitic transformation to decrease with increasing tetragonal particle size due to the fact that larger particles result in a lower constraint from the cubic matrix on the transformation. For particularly large particle sizes, the transformation can spontaneously occur while cooling, yet again similar to the spontaneous crack formation in microcrack toughness. However, toughness can also become too low if particle size is too small resulting in a decreased rc due to higher stresses since rc ~ stress-2 during cooling. Therefore, transformational toughness contains an optimum particle size similar to the optimal grain size present for microcrack toughening.[12]

Crack repair

Toughening of a material, such as concrete, which contains numerous pre-existing cracks can be achieved by crack repair. The repair of cracks is often carried out through the infiltration under pressure of binders or resin and can also be achieved by drilling a hole at the crack tip to alleviate stress concentration. This approach turns a propagating crack in to a keyhole notch with a moderated stress concentration [13].

Effect of grains and inclusions on crack propagation

Propagation of cracks in grains

The presence of grains in a material can affect its toughness by affecting the way cracks propagate. In front of a crack, a plastic zone can be present as the material yields. Beyond that region, the material remains elastic. The conditions for fracture are the most favorable at the boundary between this plastic and elastic zone, and thus cracks often initiate by the cleavage of a grain at that location.

At low temperatures, where the material can become completely brittle, such as in a body-centered cubic (BCC) metal, the plastic zone shrinks away, and only the elastic zone exists. In this state, the crack will propagate by successive cleavage of the grains. At these low temperatures, the yield strength is high, but the fracture strain and crack tip radius of curvature are low, leading to a low toughness.[12]

At higher temperatures, the yield strength decreases, and leads to the formation of the plastic zone. Cleavage is likely to initiate at the elastic-plastic zone boundary, and then link back to the main crack tip. This is usually a mixture of cleavages of grains, and ductile fracture of grains known as fibrous linkages. The percentage of fibrous linkages increase as temperature increases until the linkup is entirely fibrous linkages. In this state, even though yield strength is lower, the presence of ductile fracture and a higher crack tip radius of curvature results in a higher toughness.[12]

It is worth noting that depending on the crystal structure, this behavior can be different. For example, face-centered cubic (FCC) metals remain ductile even at low temperatures, so a plastic zone is always present.

Presence of inclusions

Inclusions in a material such as a second phase particles can act similar to brittle grains that can affect crack propagation. Fracture or decohesion at the inclusion can either be caused by the external applied stress or by the dislocations generated by the requirement of the inclusion to maintain contiguity with the matrix around it. Similar to grains, the fracture is most likely to occur at the plastic-elastic zone boundary. Then the crack can linkup back to the main crack. If the plastic zone is small or the density of the inclusions is small, the fracture is more likely to directly link up with the main crack tip. If the plastic zone is large, or the density of inclusions is high, additional inclusion fractures may occur within the plastic zone, and linkup occurs by progressing from the crack to the closest fracturing inclusion within the zone.[12]

Fracture toughness testing methods

Fracture toughness tests are performed to quantify the resistance of a material to failure by cracking. Such tests result in either a single-valued measure of fracture toughness or in a resistance curve. Resistance curves are plots where fracture toughness parameters (K,J etc) are plotted against parameters characterizing the propagation of crack. The resistance curve or the single-valued fracture toughness is obtained based on the mechanism and stability of fracture. Fracture toughness is a critical mechanical property for engineering applications. There are several types of test used to measure fracture toughness of materials, which generally utilise a notched specimen in one of various configurations. A widely utilized standardized test method is the Charpy impact test whereby a sample with a V-notch or a U-notch is subjected to impact from behind the notch. Also widely used are crack displacement tests such as three-point beam bending tests with thin cracks preset into test specimens before applying load.

The immense real-world consequence of failure of materials by fracture has motivated a variety of organization throughout the world to publish standardized procedures for fracture toughness measurements, namely ASTM, BSI, ISO, JSME. No single standard as informed through these organization is universal, so careful inspection of the standards are required before it can be applied to a specimen.

Prior to testing

There are few common points need to considered before commencing with the testing of any specimen. The design and orientation of the test specimen is one of the main points of scrutiny.

ASTM standard describes[14] five specimen configurations, namely compact specimen, disk-shaped compact specimen, single edge notched bend specimen(SENB), middle tension and arc-shaped specimen. Each specimen configuration is characterized by three dimensions, namely the crack length(a), the thickness(B) and the width(W). The values of these dimensions is determined by the demand of the particular test that is being performed on the specimen. The vast majority of the tests are carried out on either compact or SENB configuration. For the same characteristic dimensions, compact configuration takes a lesser amount of material compared to SENB.

Orientation of fracture is important because of the inherent non-isotropic nature of most engineering materials. Due to this, there may be "planes of weakness" within the material, and crack growth along this plane may be easier compared to other direction. Due to this importance ASTM has devised a standardized way of reporting the crack orientation with respect to forging axis[15]. The letters L, T and S are used to denote longitudinal, transverse and short transverse direction, where longitudinal direction coincides with forging axis. The orientation is defined with two letters the first one being the direction of principal tensile stress and the second one is the direction of crack propagation. Generally speaking, the lower bound of the toughness of a material is obtained in the orientation where the crack grows in the direction of forging axis.

It is imperative to carefully introduce a crack into the specimen to test. To apply the results of the toughness tests to the theory we need an infinitely sharp crack prior to loading. The machined cracks do not meet this criterion, i.e. they have a finite opening at the crack tip. The most effective way of introducing a sufficiently sharp crack is through cyclic loading. Fatigue cracks are initiated at the tip of machined cracks and allowed to extend till the crack length reaches its desired value. The cyclic loading is to be controlled carefully so as to not affect the actual toughness of the material through strain-hardening. This is done through choosing the cyclic loads which produces far smaller plastic zone compared to plastic zone of the main fracture. For example, according to ASTM E399 standard the maximum stress intensity Kmax should be no larger than 0.6KIC during the initial stage and less than 0.8KIC when crack approaches its final size.[16]

In certain cases grooves are machined into the sides of a fracture toughness specimen so that the thickness of the specimen is reduced to minimum of 80% of the original thickness along the intended path of crack extensions[17]. The reason is to maintain a straight crack front during R-curve test.

The four main standardized tests are described below with KIc and KR tests valid for linear-elastic fracture mechanics(LEFM) while J and JR tests valid for elastic-plastic fracture mechanics(PEFM)

Determination of plane strain fracture toughness, KIc

When a material behaves in a linear elastic way prior to failure, such that the plastic zone is small compared to the specimen dimension, a critical value of Mode-I stress intensity factor can be an appropriate fracture parameter. This method provides a quantitative measure of fracture toughness in terms of the critical plane strain stress intensity factor. The test must be validated once complete to ensure the results are meaningful. The specimen size is fixed, and must be large enough to ensure plane strain conditions at the crack tip. This limits the product forms to which the test can be applied.

In the 1960s, it was postulated that small specimens or thin sections fail under plane stress conditions, and that ''plane strain fracture'' occurs in thick sections. The ASTM E 399 test method reflects this viewpoint. Over the years, it has been taken as an indisputable fact that toughness decreases with increasing specimen size until a plateau is reached. Specimen size requirements in ASTM E 399 are intended to ensure that KIc measurements correspond to the supposed plane strain plateau. The specimen size requirements in this standard are far more stringent than they need to be to ensure predominately plane strain conditions at the crack tip. The real key to a K-based test method is ensuring that the specimen fractures under nominally linear elastic conditions. That is, the plastic zone must be small compared to the specimen cross section. Consequently, the important specimen dimensions to ensure a valid K test are the crack length a and the ligament length W-a, not the thickness B. Four specimen configurations are permitted by the current version of E 399: the compact, SE(B), arc-shaped, and disk-shaped specimens. Specimens for KIc tests are usually fabricated with the width W equal to twice the thickness B. They are fatigue pre-cracked so that the crack length/width ratio (a /W) lies between 0.45 and 0.55. Thus, the specimen design is such that all of the key dimensions, a, B, and W-a, are approximately equal. This design results in the efficient use of material, since the standard requires that each of these dimensions must be large compared to the plastic zone.

Plane-strain fracture toughness testing

When performing a fracture toughness test, the most common test specimen configurations are the single edge notch bend (SENB or three-point bend), and the compact tension (CT) specimens. From the above discussion, it is clear that an accurate determination of the plane-strain fracture toughness requires a specimen whose thickness exceeds some critical thickness (B). Testing has shown that plane-strain conditions generally prevail when:


Where: B is the minimum thickness that produces a condition where plastic strain energy at the crack tip in minimal
KIC is the fracture toughness of the material
?YS is the yield stress of material

The test is performed by loading steadily at a rate such that KI increases steadily from 0.55 to 2.75 (MPa)/s. The load and the crack mouth opening displacement(CMOD) is noted and the test is continued till the maximum load is reached. The critical load, PQ is calculated through specialized data reduction method from the load vs CMOD plot. Then we calculate a provisional toughness KQ given as . The function is a dimensionless function of a/W. This function is given in polynomial form in E 399 standard, Function for compact test geometry can be found here [19]. This provisional toughness value is recognized as the valid one when the validity requirements are met, which include


When a material of unknown fracture toughness is tested, a specimen of full material section thickness is tested or the specimen is sized based on a prediction of the fracture toughness. If the fracture toughness value resulting from the test does not satisfy the requirement of the above equation, the test must be repeated using a thicker specimen. In addition to this thickness calculation, test specifications have several other requirements that must be met (such as the size of the shear lips) before a test can be said to have resulted in a KIC value.

When a test fails to meet the thickness and other test requirements that are in place to insure plane-strain condition, the fracture toughness value produced is given the designation KC. Sometimes it is not possible to produce a specimen that meets the thickness requirement. For example, when a relatively thin plate product with high toughness is being tested, it might not be possible to produce a thicker specimen with plain-strain conditions at the crack tip.

Plane-stress and transitional-stress states

For cases where the plastic energy at the crack tip is not negligible, other fracture mechanics parameters, such as the J integral or R-curve, can be used to characterize a material. The toughness data produced by these other tests will be dependent on the thickness of the product tested and will not be a true material property. However, plane-strain conditions do not exist in all structural configurations and using KIC values in the design of relatively thin areas may result in excess conservatism and a weight or cost penalty. In cases where the actual stress state is plane-stress or, more generally, some intermediate- or transitional-stress state, it is more appropriate to use J integral or R-curve data, which account for slow, stable fracture (ductile tearing) rather than rapid (brittle) fracture.

Uses of plane-strain fracture toughness

KIC values are used to determine the critical crack length when a given stress is applied to a component.

Where: sc is the critical applied stress that will cause failure
KIC is the plane-strain fracture toughness
Y is a constant related to the sample's geometry
a is the crack length for edge cracks

or one half crack length for internal crack

Determination of fracture toughness R-curve, K-R

The specimen showing stable crack growth shows an increasing trend in fracture toughness as the crack length increases(ductile crack extension). This plot of fracture toughness vs crack length is called the resistance(R)-curve. ASTM E561 outlines a procedure for determining toughness vs crack growth curves in materials[20]. This standard does not have a constraint over the minimum thickness of the material and hence can be used for thin sheets however the requirements for LEFM must be fulfilled for the test to be valid. The criteria for LEFM essentially states that in-plane dimension has to be large compared to the plastic zone. There is a misconception about the effect of thickness on the shape of R curve. It is hinted that for the same material thicker section fails by plane strain fracture and shows a single-valued fracture toughness, the thinner section fails by plane stress fracture and shows the rising R-curve. However, the main factor that controls the slope of R curve is the fracture morphology not the thickness. In some material section thickness changes the fracture morphology from ductile tearing to cleavage from thin to thick section, in which case the thickness alone dictates the slope of R-curve. There are cases where even plane strain fracture ensues in rising R-curve due to "microvoid coalescence" being the mode of failure.

Negligible plastic zone

The most accurate way of evaluating K-R curve is taking presence of plasticity into account depending on the relative size of the plastic zone. For the case of negligible plasticity, the load vs displacement curve is obtained from the test and on each point the compliance is found. The compliance is reciprocal of the slope of the curve that will be followed if the specimen is unloaded at a certain point, which can be given as the ratio of displacement to load for LEFM. The compliance is used to determine the instantaneous crack length through the relationship given in the ASTM standard. The crack length can also be measured through optical means. Which is followed by KI calculation using the formula


Modification considering plasticity

The stress intensity should be corrected by calculating an effective crack length. ASTM standard suggests two alternative approaches. The first method is named Irwin's plastic zone correction. Irwin's approach describes the effective crack length to be

where = Uni-axial yield strength of the material. -------------------[2] [13]

Irwin's approach leads to an iterative solution as K itself is a function of crack length.

The other method, namely the secant method, uses the compliance-crack length equation given by ASTM standard to calculate effective crack length from an effective compliance. Compliance at any point in Load vs displacement curve is essentially the reciprocal of the slope of the curve that ensues if the specimen is unloaded at that point. Now the unloading curve returns to the origin for linear elastic material but not for elastic plastic material as there is a permanent deformation. The effective compliance at a point for the elastic plastic case is taken as the slope of the line joining the point and origin( i.e the compliance if the material was an elastic one). This effective compliance is used to get an effective crack growth and the rest of the calculation follows the equation

The choice of plasticity correction is factored on the size of plastic zone. ASTM standard covering resistance curve suggests using Irwin's method is acceptable for small plastic zone and recommends using Secant method when crack-tip plasticity is more prominent. Also since the ASTM E 561 standard does not contain requirements on the specimen size or maximum allowable crack extension, thus the size independence of the resistance curve is not guaranteed. Few studies show that the size dependence is less detected in the experimental data for the Secant method.[21]

Determination of JIC

Strain energy release rate per unit fracture surface area is calculated by J-integral method which is a contour path integral around the crack tip where the path begins and ends on either crack surfaces. J-toughness value signifies the resistance of the material in terms of amount of stress energy required for a crack to grow. JIC toughness value is measured for elastic-plastic materials. Now the single-valued JIC is determined as the toughness near the onset of the ductile crack extension( effect of strain hardening is not important). The test is performed with multiple specimen loading each of the specimen to various levels and unloading. This gives the crack mouth opening compliance which is to be used to get crack length with the help of relationships given in ASTM standard E 1820, which covers the J-integral testing[22]. Another way of measuring crack growth is to mark the specimen with heat tinting or fatigue cracking. The specimen is eventually broken apart and the crack extension is measured with the help of the marks.

The test thus performed yields several Load vs Crack Mouth Opening Displacement (CMOD) curve, which are used to calculate J as following:-

The linear elastic J is calculated using

and K is determined from where BN is the net thickness for side-grooved specimen and equal to B for not side-grooved specimen

The elastic plastic J is calculated using

Where =2 for SENB specimen

bo is initial ligament length given by the difference between width and initial crack length

APl is the plastic area under the load-displacement curve.

Specialized data reduction technique is used to get a provisional JQ. The value is accepted if the following criterion is met

Determination of tear resistance (Kahn tear test)

The tear test (e.g. Kahn tear test) provides a semi-quantitative measure of toughness in terms of tear resistance. This type of test requires a smaller specimen, and can, therefore, be used for a wider range of product forms. The tear test can also be used for very ductile aluminium alloys (e.g. 1100, 3003), where linear elastic fracture mechanics do not apply (see properties in practice).

Fracture toughness of AISI steel

The fracture toughness of AISI 4340 steel has been determined by several methods, i.e. (i)Jr curve, (ii)?r curve, (iii) Kr curve, (iv) stretch zone size measurements (v) non-linear energy method of Poulose et al. and by (vi) a new procedure proposed recently by Banerjee. Compact tension specimens with TL orientation have been used. All the specimens used satisfied the ASTM E813 test size requirements. Applicability of various fracture toughness estimation procedures like (i) Hanhn and Rosenfield, (ii) Rolfe and Barsom and (iii) equivalent energy rate method of Bucci et al. have been examined. These values have been compared with true fracture toughness of the material obtained by ASTM E399 test procedure.[23]

Comparison of various conventional test methods indicate multiple specimen curve method gives most consistent results and these values are within +15% of the true fracture toughness value. Out of all estimation procedures Rolfe and Barsom's method appears to be best, giving number within +8% of the true fracture toughness value. Non-linear energy method was found to give a fracture toughness value consistent with true fracture toughness of the material.

Other methods for determining fracture toughness

  • ASTM C1161 Test Method for Flexural Strength of Advanced Ceramics at Ambient Temperature
  • ASTM C1322 Practice for Fractography and Characterization of Fracture Origins in Advanced Ceramics
  • ASTM E4 Practices for Force Verification of Testing Machines
  • ASTM E112 Test Methods for Determining Average Grain Size
  • ASTM E177 Practice for Use of the Terms Precision and Bias in ASTM Test Methods
  • ASTM E337 Test Method for Measuring Humidity with a Psychrometer (the Measurement of Wet- and Dry-Bulb Temperatures)
  • ASTM E399 Test Method for Plain-strain Fracture Toughness of Metallic Materials
  • ASTM E691 Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
  • ASTM E740 Practice for Fracture Testing with Surface-Crack Tension Specimens
  • ASTM E1823 Terminology Relating to Fatigue and Fracture Testing
  • IEEE/ASTM SI 10 Standard for Use of the International System of Units (SI) (The Modern Metric System)[24]
  • ISO 28079:2009, the Palmqvist method, used to determine the fracture toughness for cemented carbides.[25]

Strain energy release rate

For two-dimensional problems (plane stress, plane strain, antiplane shear) involving cracks that move in a straight path, the mode I stress intensity factor is related to the energy release rate, also in mode I, by

where is the Young's modulus and for plane stress and for plane strain.[13]

See also


  1. ^ Hertzberg, Richard W. (December 1995). Deformation and Fracture Mechanics of Engineering Materials (4th ed.). Wiley. ISBN 0-471-01214-9.
  2. ^ Sérgio Francisco dos Santos; José de Anchieta Rodrigues (2003). "Correlation Between Fracture Toughness, Work of Fracture and Fractal Dimensions of Alumina-Mullite-Zirconia Composites". Materials Research. 6 (2): 219-226. doi:10.1590/s1516-14392003000200017.
  3. ^ Courtney, Thomas (2005). Mechanical Behavior of Materials. Chapter 9: Waveland Press. pp. 433-436. ISBN 1-57766-425-6.
  4. ^ Kaufman, J. Gilbert (2015), Aluminum Alloy Database, Knovel, retrieved 2019
  5. ^ ASM International Handbook Committee (1996), ASM Handbook, Volume 19 - Fatigue and Fracture, ASM International, p. 377
  6. ^ Titanium Alloys - Ti6Al4V Grade 5, AZO Materials, 2000, retrieved 2014
  7. ^ AR Boccaccini; S Atiq; DN Boccaccini; I Dlouhy; C Kaya (2005). "Fracture behaviour of mullite fibre reinforced-mullite matrix composites under quasi-static and ballistic impact loading". Composites Science and Technology. 65 (2): 325-333. doi:10.1016/j.compscitech.2004.08.002.
  8. ^ J. Phalippou; T. Woignier; R. Rogier (1989). "Fracture toughness of silica aerogels". Journal de Physique Colloques. 50: C4-191. doi:10.1051/jphyscol:1989431.
  9. ^ Wei, Robert (2010), Fracture Mechanics: Integration of Mechanics, Materials Science and Chemistry, Cambridge University Press, ASIN 052119489X
  10. ^ Liang, Yiling (2010), The toughening mechanism in hybrid epoxy-silica-rubber nanocomposites, Lehigh University, p. 20, OCLC 591591884
  11. ^ Padture, Nitin (12 April 2002). "Thermal Barrier Coatings for Gas-Turbine Engine Applications". Science. 296 (5566): 280-284. Bibcode:2002Sci...296..280P. doi:10.1126/science.1068609.
  12. ^ a b c d e Courtney, Thomas H. (2000). Mechanical behavior of materials. McGraw Hill. ISBN 9781577664253. OCLC 41932585.
  13. ^ a b c Liu, M.; et al. (2015). "An improved semi-analytical solution for stress at round-tip notches" (PDF). Engineering Fracture Mechanics. 149: 134-143. doi:10.1016/j.engfracmech.2015.10.004.
  14. ^ E08 Committee. "Terminology Relating to Fatigue and Fracture Testing". doi:10.1520/e1823-13. Cite journal requires |journal= (help)
  15. ^ "Standard Terminology Relating to Fatigue Fracture Testing". doi:10.1520/e1823-13. Retrieved 2019.
  16. ^ "Standard Test Method for Plane-Strain Fracture Toughness of Metallic Materials". doi:10.1520/e0399-90r97. Retrieved 2019.
  17. ^ "Thickness and Side-Groove Effects on J- and ?-Resistance Curves for A533-B Steel at 93C". doi:10.1520/stp35842s. Retrieved 2019.
  18. ^ "Standard Test Method for Plane-Strain Fracture Toughness of Metallic Materials". doi:10.1520/e0399-90r97. Retrieved 2019.
  19. ^ "Stress Intensity Factors Compliances And Elastic Nu Factors For Six Test Geometries".
  20. ^ "Standard Practice for R-Curve Determination". doi:10.1520/e0561-98. Retrieved 2019.
  21. ^ Faturohman, Topan (10 April 2018). "Peranan Pramusaji Dalam Meningkatkan Kepuasan Tamu di Saffron Restoran Four Points by Sheraton Hotel Bandung". doi:10.31237/ Cite journal requires |journal= (help)
  22. ^ "Standard Test Method for Measurement of Fracture Toughness". doi:10.1520/e1820-01. Retrieved 2019.
  23. ^ Engineering Fracture Mechanics, Volume 25, Issue 4, 1986
  24. ^ NIST SRM 2100 Fracture Toughness of Ceramics
  25. ^ ISO 28079:2009, Palmqvist toughness test, Retrieved 22 January 2016

Other references

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