Novel shear tools for viscoelastic characterization of packaging polymers
Introduction
Polymer cracking, interface delamination and thermal fatigue are the major reliability concerns for microelectronic packages, caused mainly by mismatch in thermal expansion coefficients between the constituents. Packaging polymers are usually introduced to improve the thermo-mechanical reliability of the package and/or for environmental protection. However, the curing process of the applied polymers induces residual stress- and strain fields. To investigate the influence of the residual stress- and strain fields on the failure predictions and to optimize the product for reliability, cure-dependent viscoelastic constitutive relations for the applied polymers have recently been developed [1], [2], [3]. These describe the full temperature and conversion dependent viscoelastic behavior.
The experimental investigation of the shear relaxation modulus function, being one of the important model parameter functions, is complicated as at the beginning of cure the polymer material is in the liquid state and remains in a more or less liquid state during a first period of time, up to the so-called gelpoint and then gradually solidifies. This restricts the choice of possible sample geometries and measurement methods. Therefore, two different approaches are generally applied. One approach uses (solidified) molded samples of different degree of cure to be investigated thermal–mechanically. Disadvantage of such an approach is that it is rather time consuming. The second approach, which is not affected by this disadvantage, uses continuous monitoring of the thermal–mechanical properties from fluid to fully cured state, by applying the liquid resin in the (small) gap between parallel plates and then applying Dynamic Mechanical Analysis (DMA) during the curing process. So far, the second method was used with torsional shear deformation or with a double simple shear test set-up. However, the extremely large relative change of the shear relaxation modulus function during cure (from liquid to fully cured), cannot adequately be followed by commercially available DMA test facilities, for small-gap specimen. Therefore, in particular the measurements for larger modulus values are lacking accuracy. With application of a newly developed “Sandwich Beam” specimen, where the liquid resin is applied in the small gap between parallel leaf springs, the accuracy problem is completely solved. The interpretation of measurement data requires the theoretical solution of the viscoelastic behavior of the sandwich beam during DMA. For this an adequate approximation is proposed and verified through FEM viscoelastic simulations.
Section snippets
Simple shear tool
The initially liquid state of the resin requires a shear tool which prevents resin leakage. Initially, a simple shear tool was used for the characterization which consisted of two fixed parallel plates between which a third plate could move up and downwards. The two gaps between the fixed and the moving plates were filled with liquid resin. In this case surface tension prevents the sample from leaking. The middle plate was mounted to the actuator of a DMA facility, whereas the two outer plates
Sandwich beam set-up
The simple shear tool performs well for the lower shear modulus range. For higher modulus levels an alternative tool has to be developed which allows a shear stress to be reached at a much lower sample stiffness values. This cannot be realized by simply reducing the cross-sectional area since then inaccuracies in the sample shape will result in unacceptable errors in the modulus value. Also the ability to widen the gap is limited because of leakage problems. Therefore a completely different
Application to experimental data
In order to find out how the simple shear tool equation (Eq. (7)) and the sandwich beam equation (Eq. (36)) work out in practice we prepared an epoxy system consisting of stoichiometric amounts of novolac epoxy EPN 1180 (Ex Vantico) and bisphenol-A. As a catalyst 0.5 wt% TPP per 100 gram epoxy was used. These components were carefully mixed, degassed and applied in liquid form between the gaps of the SST and the SBT, respectively. The materials were cured to full extent inside the two shear
Conclusions
In this paper, correction equations for the effect of a finite clamp stiffness on the measured mechanical properties were derived. It was shown that the correction equations for the Simple Shear Tool could be used until the sample stiffness becomes comparable to that of the clamps or, more precisely, up to Ktot/Kclamp = 0.5. For higher sample stiffnesses, as occurring when a material solidifies, modulus values as measured with the Simple Shear Tool are no longer reliable since they become too
Acknowledgements
The authors acknowledge the European Community for their financial support (Mevipro project GRD1-2001-40296) and Vantico for the supply of the epoxy resin.
References (5)
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- Jansen KMB et al. Cure-temperature and time dependent constitutive modeling of moulding compounds. In: Proceedings of...
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