2. Material and Methods
The material used in this work was an AA2198-T851 sheet with 2.0 mm thickness. This third-generation Al-Li alloy patented by Constellium (formerly Alcan) with the trademark “Airware” is one of the most advanced Al-Li alloys commercially available currently. The T851 temper corresponds to solution heat treatment followed by quenching, stress relieving by stretching and then artificial aging. The chemical composition of the alloy, determined via inductively coupled plasma mass spectrometry (ICP Vista MPX, Varian, Palo Alto, CA, USA) in a previous work [
16], conforms to AMS 4412 standard and includes, as main elements, the following (wt. %): 1.01 Li, 3.68 Cu, 0.305 Mg, 0.12 Zr, 0.03 Si, 0.027 Ti, 0.08 Fe and 0.01 Zn (Al–remainder). The tensile properties of the AA2198-T851 sheet material are: Young’s modulus = 81 GPa, yield stress = 439 MPa and ultimate tensile strength = 480 MPa [
16].
The local heating treatments were performed using an IPG Photonics (Oxford, MA, USA) Yb:fiber laser model YLR-2000, with a maximum power of 2 kW. The optical head was positioned 12.2 mm above the focal length, resulting in a Gaussian spot diameter of 2 mm on the surface of the aluminum sheet samples, which were previously spray painted with carbon black to ensure uniform absorption of the laser heating. The laser irradiation experiments were performed in a computerized numerical control (CNC) table. In order to find the most promising process parameters, some preliminary tests were conducted in which various combinations of the laser powers (150, 200 and 250 W) and the optical head displacement speed over the sheet surface (1, 2.5, 5 and 10 mm/s) were set. The objective of these tests was to determine laser energy densities that produce visible heating lines without undesirable effects such as excessive melting of the material (as in welding) or visible bending of the sheet samples. By means of visual inspection, the resulting interaction between the laser beam and the sheet material was rated as weak (any effect), ideal, or destructive (too much melting). Some combinations considered optimal were performed in quadruplicate for statistical purposes.
Microstructural analyses and hardness measurements were performed in cross section samples taken from the preliminary test sheets. The samples were sectioned transversely to the heating lines by abrasive cutting with a low-speed diamond saw, cold mounted in epoxy resin and then mechanically polished and etched (10 s) with Keller reagent (190 mL distilled water, 5 mL nitric acid, 3 mL hydrochloric acid and 2 mL hydrofluoric acid) for microstructure visualization using a Leica (Wetzlar, Germany) DM4000 optical microscope. The hardness measurements, taken approximately 100 μm below the laser treated surface, were performed using a Buehler (Lake Bluff, IL, USA) Micromet 2004 Vickers hardness tester with 50 gf load and 10 s dwell time.
Compact tension C(T) specimens, cut in the T-L orientation, were adopted for the FCG tests. The specimens were manufactured by electrical discharge machining including the notch with a root radius of 0.25 mm. From the preliminary tests, two laser beam heating conditions were selected for the fatigue specimens, namely, the displacement speeds of 1 mm/s and 10 mm/s, both with a laser power level of 200 W. Just like the preliminary test sheets, the FCG specimens were spray painted with carbon black prior to laser irradiation. Each specimen was irradiated with two heating lines on the same side and each heating line was produced by a single laser pass. The position and number of the heating lines were based on the previous work by Cunha and Lima [
14]. For comparison, some of the FCG specimens were left in the “as-received” condition (i.e., without laser beam heating line). The specimen dimensions, including the heating lines position, are shown in
Figure 1.
The FCG tests, conducted in accordance with the ASTM E647-15e1 standard at room temperature in laboratory air, were performed with constant load amplitude under force control using an MTS (Eden Prairie, MN, USA) 810 servo-hydraulic machine. The fatigue pre-cracking of the specimens was performed prior to the FCG tests, by letting a pre-crack to grow about 15 mm from the notch tip and ensuring that the final maximum load during pre-crack was less than the maximum load of the test, for which the data were obtained. The test frequency was kept constant at 5 Hz and the loading waveform was sinusoidal. Two load ratios (min/max) were adopted for the tests: R = 0.1 and 0.5. The compliance method of crack length monitoring was used during the tests. The crack growth rate was calculated using both the secant and the seven-point incremental polynomial methods.
4. Discussion
For clearness purposes, Vickers hardness profiles for the laser speeds of 1 mm/s and 10 mm/s are plotted again in
Figure 9. In these conditions, the hardness was also reduced, although not so much as in the samples presenting a fusion zone (see
Figure 3). Moreover, the two conditions resulted in clearly distinct hardness profiles. These features may be discussed based on the premise that hardness in AA2198 depends effectively on the density and size of the strengthening precipitates, which can be strongly affected by the local thermal cycles experienced by the samples during the laser heating.
Zhao et al. [
17] evaluated the effect of laser pressure weld in AA2198, showing the relationship between hardness and precipitation evolution in the weld metal and in the heat affected zones (HAZ). By means of transmission electron microscopy analyses, they found that the base material AA2198 with 155–170 HV contained a high density of T
1 phase, medium density of needle-shaped θ’ and spherical δ’ phases and a low density of spherical β’ and needle-shaped S’ phases. The distribution of the hardening precipitates significantly changed, in different ways, in the weld metal and in various positions of the HAZ. This was attributed to the fact that these phases are formed and dissolve at distinct temperature ranges. Besides, the softening in the welded region was essentially due to the reduced density of fine T
1 precipitates, associated with their dissolution or coarsening [
17]. The presence of significantly coarsened β’, re-precipitated δ’ (during cooling) and Cu and Li solutes in a region of dissolved precipitates, among others, also contributed to the variations observed in the hardness profile. Although the present work does not deal with laser welding, the material beneath the irradiated surface is subjected to thermal cycles that can transform the hardening precipitates as well. As shown in
Figure 2, the laser heating at 1 mm/s caused a lower hardness drop in a wider area than the laser heating at 10 mm/s. Moreover, there is a hardness peak (120 HV) in the middle of the heating line produced at 1 mm/s. These features are the result of the thermal cycles experienced by the material, which in turn depends basically on the laser speed and eventually the oxidation characteristics of the carbon black layer. A detailed precipitates investigation is beyond the scope of this work.
The distinct hardness profiles observed in
Figure 2 are therefore a consequence of temperature differences in the heating lines and may also be related to differences in residual stresses and, consequently, in the fatigue crack growth behavior as previously shown. On the other hand, the effect of laser heating on the FCG rate depends also on the stress ratio, being more evident for
R = 0.1 than for
R = 0.5 (
Figure 4 and
Figure 5). In tests under the same conditions (
R and
Pmax), the life increases due to crack retardation at subcritical crack growth were approximately the following: 5% for L10-R05, 32% for L01-R05 and 30% for L10-R01. The L01-R01 test under the same
Pmax resulted in crack arrest and was resumed with a higher load. Another test with increased
Pmax = 1.6 kN was conducted for the simulation purposes. The reason for the R-effect on the performance of laser treated material regarding FCG resistance may lie in how the residual stresses affect the driving force for crack growth, as discussed in the following paragraphs. Beyond that, it was the combination of the more favorable laser heating parameters and loading condition that led the L01-R01 condition to show a better effect on restraining the fatigue crack growth.
The stress intensity factor K is a parameter of Linear Elastic Fracture Mechanics that reflects the elastic stress field in the vicinity of the crack tip as a function of the crack size itself and the nominal stress applied to the part. Bearing in mind that stress tends to infinity in the elastic asymptote, the formation of a plastic zone at the tip of the crack is considered, limiting the stress values. In a loading cycle, Δ
K relates to the difference between the stress fields acting on loading and unloading and is accepted as the driving force for fatigue crack growth as described, for example, by the well-known Paris model [
18]:
where
C,
n are fitting constants. For a given maximum load in the loading cycle, the elastic stresses in the unloading increase with the increase of
R [
19]. On the other hand, in the case of laser-treated samples, there are compressive residual stresses along the crack line, in equilibrium with the resultant tractive residual stresses acting on the heating lines. The intensity of these stresses depends, among other factors, on the laser treatment parameters, on the material properties and geometry of the specimen. For example, compressive residual stresses of −30 MPa were found in AA2198-T8 CT(100) specimens by Schnubel et al. [
13] and values between −30 MPa and −22 MPa were observed along the crack line in AA2024-T3 CT(50) specimens by Cunha and Lima [
14]. However, these measurements do not take in account possible residual stress relaxation and/or redistribution as the crack grows, which makes it difficult to model fatigue crack propagation.
A straightforward way to get around this issue when modeling FCG is to assume a constant value for residual stress along the crack path. Thus, it is considered that this compressive static field, superimposed on the applied load, acts by reducing the normal stresses ahead of the crack described by the stress intensity factor range. Two possible situations may arise from this superposition when considering the effective K values. If the residual stress is sufficient only to reduce the effective values of Kmax and Kmin without zeroing the latter, we have a situation where ΔKef = ΔK, but with an effective stress ratio less than the nominal, that is, Ref < R, and, in this case, the reduction in the crack growth rate tends to be modest or negligible. On the other hand, if the compressive residual stress is sufficient to make Kmin negative, the zero value is adopted for this parameter, resulting in the effective stress intensity factor range also being smaller than the nominal one, that is, ΔKef < ΔK, leading to a more expressive reduction in the crack growth rate, as observed here for the R = 0.1 tests.
In order to model FCG for this loading condition, numerical simulations of crack growth were performed. To do so, initially the fitting parameters for the Paris equation were determined for the AR-R01 test condition, resulting in
C = 1.57 × 10
−10 and
n = 2.318. Then the crack length versus number of cycle curves can be determined by numerical integration and fits very well to experimental data, as shown in
Figure 10. For the laser treated conditions L10-R01 (
Pmax = 800 N) and L01-R01 (
Pmax = 1.6 kN), the crack growth curves were obtained by adopting the AR-R01 fitting parameters and superposing in Δ
K calculations a uniformly distributed compressive stress acting from the initial crack length up to
a = 27.5 mm. The compressive stresses for each condition were determined by a trial-and-error bisection method in which the effective Δ
K and
R values were determined by subtracting a chosen compressive load
Prc from
Pmax and
Pmin and adopting the value zero for the latter in case of negative result. The obtained results were
Prc = −180 N for L10-R01 and
Prc = −390 N for L01-R01 condition. The numerical simulations resulting from this simple method are shown in
Figure 11 and
Figure 12 and proved suitable to reproduce the experimental results. Note that, by superposing the compressive load −390 N on the loading condition that resulted in crack arrest (
Figure 4), the corresponding apparent threshold observed in Δ
K (see
Figure 6) would be recalculated as about 6.0 MPa·m
0.5, which is a reasonable value. Additionally, the individual fitting parameters for all of the test conditions to the Paris model were calculated and presented in
Table 1 to allow a comparative view.