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Debonding

Debonding (also called dewetting) is one mechanism of the failure of filler reinforced composites which are subjected to either continuous stress or fluctuating stresses. Debonding may also be used as a method of production for some of the materials discussed in Section 7.3. [Pg.380]

15 gives a simple description of the stress acting on an isolated particle. In reality, more particles are involved in the dissipation of local stresses in filled [Pg.380]

The rate of debonding decreases as the number of debonded particles increases and as the stress increases. The debonding constants characterize the interaction and the influence of neighboring particles. Their values depend on the filler concentration and on the adhesion of the filler to the matrix. The volume increase due to debonding is given by the equation  [Pg.383]

The volume increase depends on the filler fraction and on the applied strain. This is confiimed in practice. Debonding correlates with loss of stiffness. The first part of the stress-strain curve (elastic stage) is related to the strains beyond which debonding occurs. In glass bead filled polypropylene, this strain was 0.7%.  [Pg.383]

In mixtures of particles, the stress of debonding is not uniform. Higher stress is needed to debond from smaller particles. Adhesion is inversely proportional to the cube root of the diameter of the particles. Experiments confirmed that large particle sized filler decreased the tensile strength of composites. The filler concentration effect is not linear. Up to a certain concentration, filler did increase the tensile properties but beyond certain level there is a reverse effect. This may relate to the interactions described in previous sections where the quality of bonding (weak or strong) depended on filler concentration. [Pg.383]


Figure I represents a two-dimensional damage distribution of an impact in a 0/90° CFRP laminate of 3 mm thickness. Unlike in ultrasonic testing, which is usually the standard method for this problem, there is no shadowing effect on the successive layers by delamination echos. With the method of X-ray refraction the exact concentration of debonded fibers can be calculated for each position averaged over the wall thickness. Additionally the refraction allows the selection of the fiber orientation. The presented X-ray refraction topograph detects selectively debonded fibers of the 90° direction. Figure I represents a two-dimensional damage distribution of an impact in a 0/90° CFRP laminate of 3 mm thickness. Unlike in ultrasonic testing, which is usually the standard method for this problem, there is no shadowing effect on the successive layers by delamination echos. With the method of X-ray refraction the exact concentration of debonded fibers can be calculated for each position averaged over the wall thickness. Additionally the refraction allows the selection of the fiber orientation. The presented X-ray refraction topograph detects selectively debonded fibers of the 90° direction.
Fig. 1 High re.solution X-ray refraction topography of low energy impact (5J) at CFRP epoxy laminate. Image area 2 mm X 4 mm. Horizontal resolution 0.2 mm. The image represents selectively an area of debonded fibers of vertical fiber orientation. Fig. 1 High re.solution X-ray refraction topography of low energy impact (5J) at CFRP epoxy laminate. Image area 2 mm X 4 mm. Horizontal resolution 0.2 mm. The image represents selectively an area of debonded fibers of vertical fiber orientation.
Fig. 2 X-ray refraction topographs of a series of /OyPOj/s samples of different impact energies. The total damage of the laminates is characterized by addition of all debonded layers of0° and 90° fiber direction. Fig. 2 X-ray refraction topographs of a series of /OyPOj/s samples of different impact energies. The total damage of the laminates is characterized by addition of all debonded layers of0° and 90° fiber direction.
Fig. 3 Refraction values of both (0°+ 90°) fiber directions with respect to impact energy per layer. The fiber/matrix debonding of CFRP laminates correlates significantly to the impact energy per volume (energy density). Fig. 3 Refraction values of both (0°+ 90°) fiber directions with respect to impact energy per layer. The fiber/matrix debonding of CFRP laminates correlates significantly to the impact energy per volume (energy density).
Another consideration is the difference in thermal expansion between the matrix and the reinforcement. Composites are usually manufactured at high temperatures. On cooling any mismatch in the thermal expansion between the reinforcement and the matrix results in residual mismatch stresses in the composite. These stresses can be either beneficial or detrimental if they are tensile, they can aid debonding of the interface if they are compressive, they can retard debonding, which can then lead to bridge failure (25). [Pg.48]

Carbon is a commonly used and successful weak interfacial coating. For high temperature appHcations, however, carbon is not the best solution, because it oxidizes, leaving a physical gap between the reinforcement and the matrix or allowing interfacial reactions that result in a strong interface bond. Much research has been conducted to develop alternative high temperature debond coatings, with tittle success to date. [Pg.49]

Artefacts Damaged piece of GFRP to show opacity caused by debonding. [Pg.293]

Fig. 1. (a) Adhesive vs. cohesive failure, (b) Close-up view of adhesive failure in the pre.sence of an interphase. The locus of failure may be adjacent to or within the interphase (as shown), and particles of material may be ejected during the debonding process. [Pg.2]

Fig. 16. Extensive deformation of foam core during debonding. Fig. 16. Extensive deformation of foam core during debonding.
The deformation of the core significantly increases the peel force during debonding (see Fig. 16). [Pg.516]

The foam typically becomes the locus for failure during debonding. [Pg.516]

Upon peeling, each particle dissipates energy by stretching to several times its diameter before debonding from the surface. [Pg.524]


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Analysis debonding

Cathodic debonding

Complete debonding

Conditions of Debonding

Cooling debonding

Crack tip debond stress

Crack-induced interfacial debonding

Creep Debonding

Damage, interfacial debonding

Debond

Debond

Debond Process

Debond area

Debond criteria

Debond energy

Debond energy measurements

Debond length

Debond stress

Debonded morphology

Debonded particles

Debonding agents

Debonding and pull-out

Debonding angle

Debonding behavior

Debonding damage

Debonding mechanisms

Debonding of fibers

Debonding of fibres

Debonding of particles

Debonding rubber particles

Debonding specimens

Detection of Wet Debonding

Durability: subcritical debonding

End-zone debonding

Energy debonding

Example Temperature change for buckling of a debond

Failure Mechanisms Due to Debonding

Fiber matrix debonding

Fiber reinforced polymers debonding

Fiber-Matrix Interface Debonding in Mode II Shear

Fibre debonding

Fillers debonds

Infinitesimal debond length

Initial debond stress

Interface debond criterion

Interface debonding

Interfacial debonding

Interfacial debonding alumina composites

Interfacial: debonding 19 layers

Large debond energy

Maximum debond length

Maximum debond stress

Model debonding

Parameters, debond length

Partial debond model

Partial debond stress

Partial debonding

Partially debonded interface

Particle debonding

Particle/matrix debonding

Post-debond Friction

Post-debonding friction

Pressure sensitive adhesive debonding

Rate of debonding

Resistance to Debonding in the Ultimate Limit State

Resistance to debonding

Simulation debonding

Small debond energy behavior

Stable debonding process

Strength debonding

Stress debonding

Tensile debonding mechanism

Two-way Debonding Phenomenon

Two-way debonding

Verification of Safety Following Debonding

Whisker-matrix interface debonding

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