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    Journal of Composite

    http://jcm.sagepub.com/content/39/16/1417The online version of this article can be found at:

    DOI: 10.1177/0021998305050432

    2005 39: 1417Journal of Composite MaterialsC. Kyle Berkowitz and W. Steven Johnson

    Fracture and Fatigue Tests and Analysis of Composite Sandwich Structure

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    On behalf of:

    American Society for Composites

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    Fracture and Fatigue Tests and Analysisof Composite Sandwich Structure

    C. KYLE BERKOWITZ*

    G. W. Woodruff School of Mechanical Engineering

    Georgia Institute of Technology

    Atlanta, GA 30332, USA

    W. STEVEN JOHNSON

    School of Materials Science & Engineering and

    G. W. Woodruff School of Mechanical Engineering

    771 Ferst Dr., Georgia Institute of Technology

    Atlanta, GA 30332-0245, USA

    (Received March 26, 2004)(Accepted October 13, 2004)

    ABSTRACT: A composite sandwich system is investigated in this research. Quasi-static fracture toughness and fatigue crack growth experimental and analyticalapproaches are the focus. The particular system studied is comprised of a Nomex

    (aramid fiber) honeycomb core with graphite/epoxy facesheets (skins).A modified version of the double cantilever beam (DCB) specimen geometry is

    used for experimentation. The critical strain energy release rate, Gc, is used to

    characterize the fracture toughness of the facesheetcore joint. Fatigue crack growthtesting is also performed. Novel analytical and experimental techniques are coupledand utilized to address challenges presented by the material system, especiallydifficult crack visualization. Crack length and growth can be estimated with anempirical approach, employing a compliance calibration. Experiments can also besimulated once several constants are estimated, aiding design. Many of thesetechniques can be generalized to other adhesive DCB experimentation.

    Results show that cold tests result in higher fracture toughnesses and slightlyslower fatigue crack growth rates than room temperature tests. The hot temperaturehas less significant impact. Although only a limited amount of very slow growth data(

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    INTRODUCTION

    SANDWICH STRUCTURES ARE normally composed of high strength thin skins

    (facesheets) bonded to a significantly thicker, less dense, and weaker core material.

    Sandwich structures are most useful in applications that put a premium on stiffness-

    to-weight ratios, such as in many aerospace applications. The focus of this paper is

    a sandwich structure with graphite/epoxy facesheets and a Nomex (aramid fiber)

    honeycomb core. This and similar systems appear on many commercial jets, especially as

    control surfaces. These composite structures tend to develop damage through long-term

    use, and this creates an enormous maintenance concern since the structural properties

    are strongly dependent on the bond integrity. These debonds can occur in the film

    adhesive used between the facesheets and core, or damage can occur in the core itself. The

    goal of this research program is to characterize the fracture and fatigue parameters of a

    particular material system, so that they can be incorporated into broader life predictions

    and a damage tolerant methodology. The properties were experimentally measured, as

    functions of test temperature, and novel experimental and data analysis strategies wereemphasized.

    BACKGROUND

    Sandwich structures have been widely applied in both aerospace and marine

    applications, as well as anywhere where weight and stiffness are the driving performance

    parameters. The first production parts that employed the idea of the modern sandwich

    structure were produced in the 1940s, but the basic idea existed much earlier [1]. While

    sandwich structures have been widely researched, only in the past two decades hasthis work addressed fracture and failure issues. Most of this work has focused on

    structures with foam core materials, and it has addressed both experimental fracture

    toughness determination and FEA to model failure criteria and predict parametric

    dependencies [2,3]. Sandwich buckling and post-buckling analysis has received much

    attention as well.

    Avery and Sankar [4] and Ratcliffe and Cantwell [5,6] are among the only researchers in

    the open literature who have performed experimental fracture work on Nomex-cored

    sandwich structures, which is a very common material in commercial aviation. Fatigue

    debond growth, as in the classic Paris formulations used in metals, has virtually been

    ignored or not well reported. The maintenance of commercial aircraft, which are used

    at a very high capacity for decades in many cases, seems to dictate a need for better

    characterization of structures of this type.

    Nomex aramid mechanical paper is a synthetic material composed of aramid fibers

    stabilized with a phenolic resin. Sheets are then expanded and bonded together in the

    honeycomb shape. Nomex has been shown to be very resistant to heat and moisture [7,8].

    Polymers properties are generally a function of temperature; these effects are often

    undesirable for an application. Aerospace composites are usually exposed to large

    temperature ranges that significantly affect their mechanical behavior. Johnson and

    Butkus [9] examined the compound effects of temperature and environmental aging on

    aerospace-bonded joints. These conditions can affect both fracture toughness and fatigue

    curves. Moreover, it is important to examine how environmental factors, especiallytemperature, affect aerospace composites.

    1418 C. K. BERKOWITZ ANDW. S. JOHNSON

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    EXPERIMENTAL PROCEDURES

    Materials and Specimen Preparation

    The specimens used in this research were constructed from six layers (plies) of woven

    carbon fiber-epoxy prepreg, all oriented squarely to the rectangular specimens. Each

    six-ply facesheet had a total cured thickness of1.5 mm. A thin (relative to a ply) film

    adhesive was placed between the prepreg and core, and it was co-cured with the prepreg.

    The honeycomb core had a cell size of 3.2 mm (1/8 in.), nominal density of 48 kg/m3

    (3.0 lb/ft3), and thickness of 9.5 mm (3/8 in.). The prepreg and honeycomb were Hexcel

    products W3F282-T6000 -F593 and HRH-10-1/8-3.0, respectively. The adhesive was Cytec

    Metlbond 1515-3M.

    The specimens were made from the manufactured rectangular panels, which had the

    approximate dimensions of 610 mm 483 mm 11.9 mm (24 in. 19 in. 0.47 in.). The

    panels were constructed from their layers of constituents and vacuum bagged, before being

    cured in an autoclave at 177C (350F) for 2 h at an absolute pressure of 4 atm. The co-curing of the facesheets and adhesive film created a blended interface, where there was

    not a clear boundary between the two. Their viscosities during curing allowed a certain

    amount of mixture to occur. Since the facesheets and adhesive were cured as they were

    being bonded to the core under the autoclaves pressure, the core became partially

    embedded in the facesheet/adhesive layer. This manufacturing technique likely leads to a

    stronger joint and certainly affects interface properties.

    Each specimen, which was tested in a double cantilever beam (DCB) configuration, was

    cut from a panel to a size of 152 mm 102 mm 11.9 mm (6 in. 4in. 0.47 in.), with the

    ribbon direction of the honeycomb aligning with the longer dimension; the 102 mm (4 in.)

    width was necessary to increase the loads to a reasonable level for the load cell. Pianohinges were riveted to the specimen to facilitate loading, and one edge was painted white to

    ease visual crack measurement. A starter crack was cut with a saw between one facesheet

    and the core, 20 mm past the load line; the crack grew in the ribbon direction. A top view

    photograph of a specimen is shown in Figure 1 (upper half of hinge is not shown to reveal

    the rivets), and a side view sketch is shown in Figure 2.

    Mechanical Testing

    Identical specimens were used for the fracture and fatigue testing; only the loading and

    data recording schemes differed. A servo-hydraulic universal mechanical testing machine

    was used, and mechanical wedge grips were used to grasp the free halves of the hinges

    used to load the specimens. Since no standards existed for fracture toughness testing

    of sandwich structures, ASTM D5528-94a was used only as a guideline when appropriate

    [10]. The specimens were loaded via the piano hinges at a constant displacement rate of

    1.27 mm/min (0.05 in./min). Loads and displacements were recorded by the testing

    software, and visual crack measurements were taken. The actuator was programmed to

    displace 0.5 mm (0.020 in.) past the point of nonlinearity, which produced crack growth.

    Then, the specimen was unloaded, and the test was repeated 1520 times per specimen,

    each giving a fracture toughness value.

    Fatigue testing was performed at 4 Hz and at anR-ratio (Pmin/Pmax) of 0.1. The goalwas to obtain da/dNversus G curves for the parameters studied. Displacement control

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    was used because the loads were relatively small for control feedback. The load was

    allowed to drop 10% before the test was stopped and restarted. At the beginning and end

    of each segment of cycles, peak loads and compliance were measured for use in analysis,

    and periodic visual measurements were taken.

    Testing was performed at hot (77C (170F)), room (21C (70F)), and cold (54C

    (65F)) temperatures, mimicking the extremes a commercial aircraft should see in

    service. The temperature-controlled environment was created with an insulated chamber

    mounted to the test machine, having both resistance heater and liquid nitrogen capabilities

    and an electronic controller. Photographs of a specimen in the testing machine are shown

    in Figure 3.

    ANALYSIS

    Fracture Toughness

    The critical strain energy release rate, Gc, was used to characterize fracture toughness

    according to:

    G P2

    2BdCda

    , 1

    Figure 1. Photograph of DCB specimen (top view).

    Core

    Piano hinges Debond

    P

    P

    11.9mm (0.47in)Facesheets

    152mm (6.0in)

    Figure 2. Sketch of DCB specimen (side view).

    1420 C. K. BERKOWITZ ANDW. S. JOHNSON

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    whereP is the applied load,B is the specimen width (102 mm),Cis the compliance, anda

    is the crack length. The critical, nonlinear load (Pc) corresponds to Gc. Equation (1)

    characterizes the energy consumed to create an increment of new crack area and applies to

    most cases of LEFM with constant specimen width. In this case, nominal area was taken;

    no consideration was given to the geometry of the honeycomb.

    Since no exact solution exists for this geometry due to asymmetry and the cores highorthotropy, dC/da was computed from a very good power law correlation that resulted

    from compliance versus crack length data for a number of specimens. A plot of the data

    used to develop this correlation is shown in Figure 4. This technique is often called the

    Berry Method [11]. This correlation is expressed as:

    C Dam, 2

    where D and m are fitting parameters. An equation of this form is easily differentiable

    for use in Equation (1). The correlation for the specimens used here was found to be:

    C 2:01 106a2:69, 3

    where C is in units of mm/N and a in mm. Equation (2) can be inverted, such that a

    measured compliance can estimate crack length. Utilizing that fact, Equations (1) and (2)

    can be combined as:

    G

    P2

    2B mD

    C

    D 1=m" #

    m1

    , 4

    Figure 3. DCB specimen loaded in test machine.

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    which reduces G to a function of machine-measured parameters and known constants.

    This implies that the manual measurement of crack length is not needed once Equation (3)

    is known, since compliance and crack length are 1-to-1. This assumption is validated by

    the quality of the simple model of Equation (2) in fitting the actual visual measurements.

    Many other models exist to predict and correlate compliance, but a more complex model

    was not warranted here.

    It may be unusual to use measured compliances in lieu of measured cracks in determining

    applied G. It is usually preferable to apply Equation (2) with compliance as the dependant

    parameter. However, for these particular experiments, it was found that achievingrepeatable visual measurements of crack lengths and crack extensions (a) was difficult

    due to the mode of failure, specimen width, and experimental apparatus. The fracture line

    of the crack was difficult to characterize, although an approximate crack length was always

    obtainable, allowing the compliance correlation to be developed from many specimens.

    Sensitivity and repeatability are important experimental issues with fracture and fatigue

    testing, due to the strong power dependencies of the resulting properties. Since compliance

    measurement was found to have much higher relative resolution than crack measurement,

    compliance was preferred as the input to data reduction. Moreover, compliance was much

    more repeatable and reliable for use inG calculations, whereas visual crack measurements

    seemed to cause unnatural scatter in the data, again resulting from the visualization issues.Therefore, the numerical compliance calibration approach described here can be a useful

    alternative in certain experimental circumstances.

    Fatigue Crack Growth

    CRACK GROWTH RATE CALCULATIONS

    Fatigue crack growth per cycle (da/dN) can be characterized by a version of Paris

    equation [12]:

    dadN

    c G n, 5

    Compliance vs. crack length: calibration curve

    C = (2.01 x 106) a2.69

    R2= 0.965

    0

    0.1

    0.2

    0.3

    0.4

    0.5

    10 25 40 55 70 85 100 115

    Crack length (mm)

    Compliance(mm

    /N)

    Composite visual data

    from 21 DCB fracture

    toughness specimens

    Figure 4. Compliance calibration.

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    where c and n are fitting parameters, and G Gmax Gmin. In this research G,

    expanded in Equation (6), was approximately 99% ofGmaxbecause anR-ratio (Pmin/Pmax)

    of 0.1 was used: (Pmax)2 (0.1 Pmax)

    2 0.99 Pmax. Therefore, there is no significant

    distinction in this case between G and Gmax, as shown by:

    G P2max P

    2min

    2B

    dC

    da Gmax: 6

    Evaluating G utilizing the compliance calibration technique was performed identically as

    in the monotonic fracture testing, and the applied G was calculated using Equation (6).

    Pmax and Pmin were obviously used instead of the critical nonlinear Pc, which results in

    quasi-static fracture failure.

    Perhaps more useful than using compliance to correlate with crack length is using

    compliance changes to correlate with crack growth. This is particularly valuable when

    visual measurements of cracks are difficult, and it also allows for greater automation. The

    use of compliance changes to calculate da/dNis fairly straightforward. Compliance was

    measured frequently during the fatigue testing to ensure that incremental increases were

    captured. Compliance was measured at monotonic test speeds, because this allowed for

    much greater resolution. Loads were chosen to easily avoid Pc

    for a given condition.

    Small increases in compliance allows for estimation of small changes in crack length to

    be performed. The measuring of small changes in crack length is important because it

    generates more data per specimen and lessens load drop effects, which are described later

    in this paper. Equation (7) can be used to express a change in crack length during a

    segment of cycles, from cycle N1 to N2, in terms of compliance increase from C1 to C2.

    a12 C2=D1=m C1=D

    1=m, 7

    whereD andm are defined in Equation (2). da/dN is simply evaluated with Equation (7)

    and using the machine count of cycles, N N2 N1.

    It is worth noting that this technique estimates a change in crack length from a change

    in compliance, not the crack length itself from compliance measurements as in the

    monotonic case. This fact decreases the sensitivity ofda/dNto possible crack measurement

    errors from the compliance calibration expression. There are many potential numerically

    more sophisticated ways of performing these calculations, although they were not

    necessary for the work presented here. Numerical differentiation for these purposes are

    further documented in ASTM E647-00 [13].

    LOAD SHEDDING EFFECTS AND EXPERIMENTAL STRATEGY

    As displacement-controlled testing results in load shedding, care must be taken to

    ensure that the applied range ofG is approximately constant for eachda/dNdata point.G

    drops dramatically with load, so frequent monitoring of load and compliance is prudent;

    however, it is not clear how many cycles should pass between each measurement of a

    da/dNdata point. If this is performed too often, machine noise could become noticeable

    and interfere with the desired material property. If this is performed too infrequently, G

    might reduce dramatically during segments of cycles used in da/dN calculations, which

    would make the data difficult to interpret. The Gat the beginning and ending of a segmentof crack should be calculated and the consequences of assumptions considered.

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    There is some question as to how much the G should be allowed to drop in a

    displacement-controlled test before taking measurements. It is impractical to take

    measurements constantly, which would be time consuming and create noise in da/dN

    data. Obviously, a resolvable growth in crack length must be allowed to take place over

    time as G falls. It is best to understand the falling driving force behavior and

    incorporate it into the experimental strategy. The effect of changes in G can be

    thought of on a loglog plot of Equation (5), which is linear with slope n. A change in

    log (G) is equal to log {(G1/G2)}, where G1 occurs at the beginning of a cycle

    segment and G2 after load is shed. If n is assumed to be 4 (this can be checked after

    some data is measured), which is reasonable for many composites [9], a value of 0.0833

    for log {(G1/G2)} would result in 1/3 decades of change in log (da/dN). This seems

    somewhat reasonable, and scatter bands are often this large for general da/dN

    data. Therefore, this amount of drop in G was tolerated before taking measurements.

    Log (P21 max=P22 max) is approximately proportional to log {(G1/G2)}, so this was

    allowed to reach 0.0833 before each segment of cycles was stopped for measurement; i.e.,

    (P1max /P2max) 1.10.Additionally, a minimum compliance increase of 5% (C2/C1 1.05) was prescribed to

    occur between cycle counts used to calculateda/dN. This prevented excessive noise in the

    data by ensuring a resolvable crack extension had occurred. All data points were checked

    against these criteria. The load drop and compliance increase restriction imply there is

    only a window of cycles during which accurate data can be gathered. If approximate

    growth rates can be estimated, specific cycle counts between necessary measurements can

    be approximated.

    The largest (beginning) Gwas associated with measured da/dNgrowth for a given set

    of cycles. This may seem slightly nonconservative, but it is significantly more accurate

    than averaging because of the power nature of the Paris Law. Conservatism can be addedto the data after it is accurately calculated by adding simple safety factors. In this

    case, shifting the da/dNdata 1/3 decade upward may make sense to create a worst-case

    boundary for the measured data.

    Due to the unusual nature of the analytical approach presented here, an examination of

    the results of a hypothetical test may help evaluate the method for a particular use. If the

    compliance calibration and crack growth empirical constants, as shown in Equations (2)

    and (5), can be estimated, then the researcher can simulate the fatigue crack growth

    process and following data reduction and analysis. This can be done to aid in specimen

    design and to refine experimental strategy before an expensive and time consuming

    experimental fatigue crack growth task is begun. For instance, one common pitfall is an

    excessively compliant specimen, which can result in very high deflection not conducive

    to high-frequency fatigue testing. A fatigue simulation using the empirically derived

    constants measured for this research is shown in Table 1. Figures 5 and 6 aid the

    visualization of several parameters throughout the experiment.

    The simulation is of a single specimen, loaded in a sequence of 3 blocks. Each of these

    blocks of fatigue cycles begins at a chosen load that produces reasonably high crack

    growth rates. Then, as load is shed, the growth rates near an assumed threshold rate. Then

    the test is reset, increasing the load (and displacement) for another period of crack

    growth. Several snapshots in time are shown during the fatigue test with associated

    parameters, including cycle count (time). The compliance and da/dN are calculated via

    the assumed empirical constants, and the other parameters are derived according tothe previously mentioned analysis. Note the total time would be 57 days at 5Hz.

    1424 C. K. BERKOWITZ ANDW. S. JOHNSON

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    Table 1. Simulation of DCB fatigue crack growth test.

    Block Pmax(N) max(mm) C (mm/N) a (mm) dC/da Gmax (J/m2) da/dN N (cycles) log (N)

    1 350 2.28 0.00651 20.0 0.00088 530 8.4E-04 1 0.0

    1 280 2.28 0.00814 21.7 0.00101 390 3.1E-04 5487 3.7

    1 224 2.28 0.01018 23.6 0.00116 288 1.2E-04 21,340 4.31 179 2.28 0.01272 25.6 0.00134 212 4.4E-05 67,153 4.8

    1 143 2.28 0.01590 27.8 0.00154 156 1.7E-05 199,539 5.3

    1 115 2.28 0.01988 30.2 0.00178 115 6.3E-06 582,102 5.8

    1 92 2.28 0.02485 32.8 0.00204 85 2.4E-06 1,687,616 6.2

    1 73 2.28 0.03106 35.7 0.00235 62 8.9E-07 4,882,280 6.7

    2 190 5.90 0.03106 35.7 0.00235 418 3.9E-04 4,882,280 6.7

    2 152 5.90 0.03882 38.7 0.00271 308 1.5E-04 4,903,257 6.7

    2 122 5.90 0.04853 42.1 0.00311 227 5.5E-05 4,963,874 6.7

    2 97 5.90 0.06066 45.7 0.00358 167 2.1E-05 5,139,043 6.7

    2 78 5.90 0.07582 49.6 0.00412 123 7.8E-06 5,645,239 6.8

    2 62 5.90 0.09478 53.9 0.00475 91 2.9E-06 7,108,020 6.9

    2 50 5.90 0.11847 58.6 0.00546 67 1.1E-06 11,335,099 7.1

    3 120 14.22 0.11847 58.6 0.00546 387 3.1E-04 11,335,099 7.1

    3 96 14.22 0.14809 63.6 0.00629 285 1.1E-04 11,379,035 7.1

    3 77 14.22 0.18511 69.1 0.00723 210 4.3E-05 11,506,000 7.1

    3 61 14.22 0.23139 75.0 0.00833 155 1.6E-05 11,872,899 7.1

    3 49 14.22 0.28924 81.5 0.00958 114 6.1E-06 12,933,147 7.1

    3 39 14.22 0.36155 88.5 0.01103 84 2.3E-06 15,997,004 7.2

    3 31 14.22 0.45193 96.2 0.01269 62 8.6E-07 24,850,797 7.4

    Load, strain energy release rate, and displacement vs. cycles

    0

    100

    200

    300

    400

    500

    0.0E+0 2.0E+6 4.0E+6 6.0E+6 8.0E+6 1.0E+7 1.2E+7 1.4E+7 1.6E+7 1.8E+7 2.0E+7

    N (cycles)

    LoadandG(lbandJ/m2)

    0

    3

    6

    9

    12

    15

    (mm) P

    G

    d

    Figure 5. Load, strain energy release rate, and displacement during fatigue simulation.

    Crack length and crack growth rate vs. cycles

    0

    30

    60

    90

    120

    0.0E+0 2.0E+6 4.0E+6 6.0E+6 8.0E+6 1.0E+7 1.2E+7 1.4E+7 1.6E+7 1.8E+7 2.0E+7

    N (cycles)

    Cracklength(mm)

    1.0E-07

    1.0E-06

    1.0E-05

    1.0E-04

    1.0E-03

    Crackgrowthrate

    (mm/cycle)

    av.N

    da/dN v. N

    Figure 6. Crack and crack growth rate during fatigue simulation.

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    A researcher could use this type of simulation to examine trade-offs among priorities and

    potential problems, and their causes.

    RESULTS

    The test matrix of the experiments performed is shown in Table 2. Eleven quasi-static

    (monotonic) fracture toughness tests were performed and seven fatigue tests. The

    experiments were performed at three different test temperatures: hot, cold, and room

    temperatures, at the combinations described in the matrix.

    Fracture Toughness

    The numerous Gc measurements from each test condition were averaged, with eachspecimen being weighted equally, and they are shown in Table 3. Many fracture toughness

    measurements for each specimen were obtained using the loadcrackunload technique

    previously described. A typical specimens loaddisplacement plot obtained for four load

    unload cycles is shown in Figure 7.

    Many materials exhibit a crack length dependence on Gc. This is generally attributed to

    a change in plastic zone shape with crack growth [14]. However, no dependence on crack

    length was found for fracture toughness for any condition studied in this work. This

    suggests that the failure can be more easily characterized by the single parameter of strain

    energy release rate. The lack of crack length dependence is often referred to as a flat

    R-curve. A plot ofGc versus crack length is shown in Figure 8.Clearly, the test temperature had an effect on fracture toughness. The cold temperature

    tests resulted in the highest fracture toughness, and the hot temperature tests had the

    Table 2. Test matrix.

    Fracture

    toughness Fatigue

    Test temperature (monotonic) crack growth

    Room temperature (21C) 6 2

    Cold temperature (

    54C) 3 2

    Hot temperature (77C) 2 3

    Total 18

    Table 3. Fracture toughness results.

    Specimens Values

    Gc,avg(J/m2)

    Room temperature (21C) 6 56 1180

    Cold temperature (54

    C) 3 62 1620Hot temperature (77C) 2 42 1160

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    ribbons of the honeycomb. There was likely not a homogeneous plastic zone, and the

    failure could have been more dominated by the aramid fibers strength than by any stressconcentrating effect within the Nomex material; however, this idea would need further

    validation. This may be an explanation for the increase in fracture toughness at the

    cold temperature; for colder temperatures generally increase a materials strength, while

    generally decreasing fracture toughness.

    In most applications, the core failure mode would be desirable and designed, since that

    would imply a high quality bond at the adhesive interface, which is important to a

    sandwich structures integrity. It is worth noting that the mode of failure and fracture

    toughness values can be strongly dependent on processing, in addition to the material

    constituents. For instance, another sandwich structure of identical facesheets, core, and

    adhesive as the one studied here, except with precured facesheets secondarily bonded to

    the core, could have considerably different failure behavior than a co-cured structure. The

    presence (or not) of an adhesive film may also have a large effect; and clearly the curing

    cycle, tooling, and constituents themselves are important parameters. Due to these

    considerations, little can be generalized for other composite sandwich structures based on

    these results. In fact, these issues warrant further research.

    Fatigue Crack Growth

    The fatigue crack growth results are presented by temperature in Figure 10. The

    resulting trends from the fatigue data are consistent with those found from the quasi-staticfracture toughness tests, and the mode of failure was the same as in the fracture case.

    Figure 9. DCB fracture surface.

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    The linear shape of the data on Figure 10 verifies the validity of the Paris crack growth

    model that was applied. The data agrees with the model well in the range of crack growth

    rates between 5 106 and 5 103 mm/cycle. A line has been sketched on the figure

    showing that an approximate Paris exponent of 3.2 fits the data well in this regime. This

    line is not intended to fit any particular set of data, but is added for visual purposes.

    A few slower growth rate data points suggest the Paris relationship is not at all

    valid below 1 106 mm/cycle, which is quite normal for many materials as threshold

    is approached. Although a true threshold was not verified, a somewhat arbitrary con-

    vention for composite fatigue is to assume 1 106 mm/cycle is significant, and a line

    Fatigue crack growth rate vs. strain energy release rate

    1.0E-07

    1.0E-06

    1.0E-05

    1.0E-04

    1.0E-03

    1.0E-02

    10 100 1000 10000

    G (J/m2)

    da/dN(mm/cycle)

    RT (21C)

    CT (54C)

    HT (77C)

    Approx. Paris fit

    Freq=4 Hz

    R=0.1

    da/dN=1.6E-12 (G)3.2

    Threshold

    GIC

    Figure 10. Fatigue crack growth data.

    Fatigue crack growth rate vs. strain energy release rate

    1.0E-06

    1.0E-05

    1.0E-04

    1.0E-03

    100 1000

    G (J/m2)

    da/dN(mm/cycle)

    RT (21C)

    CT (54C)

    HT (77C)

    Freq=4 Hz

    R=0.1

    Figure 11. Fatigue crack growth data zoomed-in.

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    corresponding to this is sketched on the figure at 70 J/m2. The data shown in this slow

    growth regime supports that a threshold effect exists. Another line at 1200 J/m2 is shown

    on the figure; this is an approximation for fracture toughness.

    Figure 11 shows a zoomed-in view of the data in Figure 10. In this plot, the data points

    can be more easily distinguished and compared. Although the overlap of the data shown in

    the figure lessens the certainty with which conclusions can be drawn, the cold temperature

    resulted in slower crack growth rates than room temperature. This would be expected

    since the cold temperature increased toughness. As shown in the figure, the hot

    temperature data seems to be highly overlapped with the room data. The point averages

    would suggest that the hot temperature resulted in faster growth, but the lack of

    separation of the scatter bands on the figure causes any conclusions to be unclear. Similar

    to the fracture toughness results, the cold temperature had a more obvious effect on the

    fatigue results than the hot temperature, relative to the baseline of room temperature.

    CONCLUSIONS

    A fracture mechanics-based approach has been utilized for characterizing a sandwich

    structure common to commercial aviation. Fracture toughness and fatigue crack growth

    testing of a particular sandwich system were performed on double cantilever beam style

    specimens. These specimens were tested at each of the three temperatures: hot (77C),

    room (21C), and cold (54C). Compliance versus crack length correlating was shown as

    an effective tool in deducing both applied strain energy release rates and crack growth

    rates from test data. Using compliance to estimate crack length can be a useful technique

    when a high resolution in compliance change with crack extension is achievable, especially

    in cases where crack tip visualization is problematic. When the necessary empiricalconstants can be estimated, a fatigue test can be simulated. This can be a valuable tool for

    the design of specimens and experimental strategy when a compliance crack length

    calibration can be utilized.

    The temperature effects on the particular sandwich system studied were significant. The

    cold temperature increased toughness and reduced fatigue crack growth rates, relative

    to room temperature. The hot temperature had relatively little impact; however, any

    marginal effects were the opposite trends as those caused by the cold. A Paris crack growth

    model fit the data well for most growth rates between near-threshold and near-Gc, and

    a flat R-curve behavior was exhibited by the material.

    The failure of all specimens tested was in the core material. This suggests that coreproperties were being measured. The mode of failure is possibly due to manufacturing

    techniques, as much as the constituents. The core was weaker than the bonding of the

    facesheets to the core. The mechanisms of failure and resulting data suggest that core

    strength is the dominant factor in the fracture mechanics properties presented in this

    paper.

    REFERENCES

    1. Zenkert, D. (ed.) (1997). The Handbook of Sandwich Construction, EMAS Ltd, UK.

    2. Falk, L. (1994). Foam Core Sandwich Panels with Interface Disbonds, Composite Structures,28(4): 481490.

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