Peel Strength of Composite Layered Joints

1988 ◽  
Vol 61 (5) ◽  
pp. 794-811 ◽  
Author(s):  
H. L. Schreuder-Stacer

Abstract 1. Master curves of R/A/R (rubber/adhesive/rubber) type adhesion tests were generated by laterally shifting the rate curves of peel response with empirically determined shift factors. The universal form of the WLF Equation (3) did not shift the data into continuous master curves, due to the individual contributions of each deforming layer. 2. For the weakly-bonded A/EPM system, rate curves were shifted into good agreement using the universal form of the WLF relation and the Tg of EPM. However, in the case of EPM/A, shift factors calculated by the WLF Equation (3) did not create a smooth master curve. Lateral shifting produced a master curve of EPM/A peel response and resulted in experimentally determined shift factors which fell between the shift factors of the EPM and the adhesive. Apparently, the EPM substrate of low Tg completely dominated the viscoelastic response of the A/EPM joint and even exerted some influence over the debonding process for the EPM/A joint, where the detaching layer was comprised only of adhesive. 3. In the case of strongly bonded chloroprene systems, CR/A/CR data were shifted laterally, but the CR/A and A/CR data shifted well with log aT values calculated from the WLF equation. Adhesive and CR Tg's were within ten degrees, and the rubber layer therefore appeared to contribute little to the overall viscoelastic response of CR/A/CR and CR/A. 4. Detachment of EPM systems was entirely interfacial, except in regions of rate where the adhesive was forced to fail in an unfavorable mode (the low-rate EPM/A experiment and the high-rate A/EPM experiment). A distinct transition of interfacial failure was observed near the glass-transition temperature of the adhesive. As the adhesive failure site changed from substrate to backing, even at the same rate and temperature, a three-fold drop in adhesive fracture energy occurred. 5. CR systems debonded through cohesive rupture of the adhesive layer at low rates. Clean interfacial failure occurred at intermediate to high peel rates. A failure site transition occurred in the same rate and temperature region as the weakly-bonded transition. This failure site change was again associated with a three-fold drop in adhesive-fracture energy. However, the actual peel force difference resulting from this transition in CR/A/CR was on the order of 1000 N/m, while the weakly bonded EPM/A/EPM system experienced a drop of approximately 100 N/m. This disparity in the two transitions suggests that the driving mechanism for the substrate-to-backing failure change is not caused simply by added adhesive bending forces in the low-rate failure mode. 6. Relative contributions of each deforming material to the total peel response for an R/A/R system cannot be determined by examining the shift factor dependence upon temperature. However, R/A and A/R models of the R/A/R detachment modes illustrate the contributions of each layer: as the adhesive debonds from the substrate, both adhesive and rubber contribute to the viscoelastic response of peel, except in the case where both layers exhibit similar Tg's; during adhesive failure from the backing, only the rubber backing contributes to the peel response.

1996 ◽  
Vol 69 (4) ◽  
pp. 577-590 ◽  
Author(s):  
H. Chun ◽  
A. N. Gent

Abstract Fracture energies have been determined for tearing through a sheet of a polysulfide elastomer, and for peeling apart two sheets bonded together with sulfur interlinks. Measurements were made over wide ranges of rate of crack propagation and test temperature. By shifting curves at various temperatures along the rate axis, using shift factors aT calculated from the “universal” form of the WLF equation, master curves were obtained for tear and peel energy vs. rate of tear or peel at the glass transition temperature Tg about −55°C. These master curves of strength vs. effective rate of crack propagation at Tg were closely similar to those obtained previously for several hydrocarbon elastomers: BR, SBR and EPR; interlinked with C-C bonds. Thus, under comparable test conditions the strength of the present polysulfide elastomer with sulfur crosslinks is similar to that for hydrocarbon elastomers with C-C crosslinks. The question then arises: Why are sulfur-vulcanized elastomers stronger in common experience than peroxide-cured ones? Possible reasons are discussed.


2018 ◽  
Vol 91 (4) ◽  
pp. 668-682 ◽  
Author(s):  
Matthias Wunde ◽  
Manfred Klüppel

ABSTRACT The crack propagation behavior of unfilled and filled styrene–butadiene rubber (SBR) in steady and dynamic tearing was investigated using tensile tests on trousers samples and tear fatigue measurements on single edge notched tension (SENT) samples, respectively. For the unfilled sample, both types of measurements indicated that the tearing energy is dominated by the viscoelastic response of the polymer. This was demonstrated by the creation of crack growth master curves using the horizontal shift factors obtained from mastering the complex modulus. The tearing energy increased with increasing crack velocity and decreasing temperature as required by the time-temperature superposition principle. The crack growth master curves followed a power law with the same exponent for steady and dynamic tearing. This exponent agrees fairly well with the exponent predicted by linear viscoelastic crack propagation theory. For steady tearing at high crack propagation rates, systematic deviations from the master curves appeared, which were attributed to flash temperature effects. For the filled SBR, which contained 50 phr carbon black, only dynamic tearing was found to be dominated by the viscoelastic response of the polymer. For steady tearing, filler networking seemed to alter crack propagation rates significantly, so that the viscoelastic fingerprint was no longer visible. For the filled sample, additional measurements with a high preload were conducted. It was demonstrated that a single master curve can be constructed, only if the (static) preload contribution is neglected and the dynamic contribution of the energy density is used for the evaluation of the tearing energy. This master curve showed two distinct slopes at high and low crack velocities. It is argued that the higher slope at low crack speeds is relevant for lifetime predictions based on the integration of the Paris–Erdogan power law. Under conditions in which the viscoelastic crack propagation holds, very slow crack growth rates can be explored at reasonable testing times by measurements at elevated temperatures.


1987 ◽  
Vol 60 (2) ◽  
pp. 227-244 ◽  
Author(s):  
R. G. Stacer ◽  
D. M. Husband ◽  
H. L. Stacer

Abstract The viscoelastic response of four highly-filled elastomers has been investigated. Small deformation dynamic testing of these materials reveals thay they are nonlinear viscoelastic, as well as thermorheologically complex. Nonlinear viscoelastic behavior was observed as a pronounced strain dependence in the range of 0.1 to 10%. The degree of this nonlinear response was quantified through a constitutive equation containing a single nonlinear factor; resultant nonlinear factors for the various materials were compared and evaluated. Thermorheologically complex behavior was displayed by slightly different shift coefficients to superpose G'′ and G″ data. An approach for calculating material resilience from the viscoelastic data was also developed and a nomographic technique presented for its application. A composite adhesive joint, consisting of two layers of a filled NBR compound bonded together by a filled putty interlayer, was also studied. It was found that both the adhesive fracture energy and the effect of interlayer thickness could be related to the loss modulus of the putty interlayer. Finally, the effect of contact time on bond strength was evaluated and results presented as a master curve of adhesive fracture energy vs. temperature-reduced contact time.


Author(s):  
J. Shi

Scatter in test results is common for relatively brittle materials such as ceramic matrix composites. The scatter may come from differences in material processing conditions, specimen machining/handling and from variations in test parameters for nominally the same test material. Large scatter in test results makes material modeling difficult. In the past, master curve concepts have been proposed to reduce scatter in tensile data and to interpret fatigue/creep results. In this paper, one such concept is examined in detail by applying it to the recent tensile test results of a SiC/SiC composite. It was found that the way to construct master curves did not apply to the CMC studied and thus a new master curve was developed to better represent the tensile data. In addition, the test data were analysed statistically based on the new master curve.


1999 ◽  
Vol 594 ◽  
Author(s):  
T. Iwasaki ◽  
H. Miura

AbstractWe have developed a molecular-dynamics technique for determining the adhesion strength of the interfaces between different materials. In this technique the extended Tersoff-type potential is applied to calculate the adhesive fracture energy defined as the difference between the total potential energy of the material-connected state and that of the material-separated state. The adhesion strength of metal/dielectric interfaces as well as metal/metal interfaces is discussed based on this fracture energy. We used this technique to determine the adhesion strength of the interfaces between ULSI-interconnect materials (Al and Cu) and diffusionbarrier materials (TiN and W). The calculated adhesive fracture energy shows that the adhesion strength increases in the order: Cu/TiN, Cu/W, Al/W, and Al/TiN. Because this result was confirmed by scratch testing on the film-laminated structure, this technique is considered to be effective for determining the adhesion strength.


2001 ◽  
Vol 16 (6) ◽  
pp. 1789-1794 ◽  
Author(s):  
T. Iwasaki ◽  
H. Miura

We have developed a molecular-dynamics technique for determining the adhesion strength of the interfaces between different materials. This technique evaluates the adhesion strength by calculating the adhesive fracture energy defined as the difference between the total potential energy of the material-connected state and that of the material-separated state. The extended Tersoff-type potential is applied to calculate the adhesive fracture energy of metal/dielectric interfaces as well as metal/metal interfaces. We used the technique to determine the adhesion strength of the interfaces between ULSI-interconnect materials (Al and Cu) and diffusion-barrier materials (TiN and W). It was also applied to determine the adhesion strength of interfaces between the interconnect materials and a dielectric material (SiO2). Because the adhesion strength determined by this technique agrees well with that measured by scratch testing, this technique is considered to be effective for determining the adhesion strength.


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