# PROGRESS TOWARDS UNDERSTANDING PSA TOWARDS UNDERSTANDING PSA FOAM TAPE DESIGN Dr. Kerstin van Wijk, ... • EVA based foam Density

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26-Apr-2018

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complicated due to the complex stress distribution and the difficulty to define a failure criterionii). 2. A fracture mechanics method with a stress-intensity factor is also not very successful mainly

because the physical basis is not very evidentii). 3. The most promising way to analyse the mechanics of the peel test is based on applying a fracture-

mechanics method using an energy-balanced approachii). In this latest approach, a value for the adhesive fracture energy, Gc, is determined, which is the energy needed to propagate a crack through a unit area of the joint. Gc should ideally be independent of

• geometric values (peel angle, thickness of the peeled element, and thickness of adhesive). However, since there is some plastic and viscoelastic deformation involved at the crack tip, it is a function of both temperature and deformation rate. In the simplest form the adhesive fracture energy can be written as:

( ) cos1)cos1( ==bP

bdaPdaGc (1)

Where P is the peeling force, is the peel angle, and b is the width of the tape. This is valid if the strip is infinitely stiff in the axial direction, but completely flexible in bending, and if the substrate is rigid.

Figure 1. Schematic of the basic peel test ii) For foam tape, the above assumptions are not true. It is therefore useful to apply a more general fracture mechanics approach:

dA

dUdUdUdUG kdsextc

= (2)

where:

dA is the increment of created area (=bda), dUext is the increment of external work (=Pda(1-cos)) dUs is the increment of change of stored energy dUd is the increment of the dissipated energy other than that in creating a new surface dUk is the increment of change of kinetic energy

The stored energy changes if the foam tape is elastically stretched by the applied force P. For foam as carrier material the deformation of the tape due to the applied force is quite significant; in addition to having an impact on the stored energy, this also reduces the peel rate and therefore, because of the viscoelastic nature of the adhesive, also the fracture energy.

• To reduce effects due to stretching of the foam tape, peel tests with foam tapes are usually performed with a polymeric film laminated on the side opposite the adhesive coated side. Therefore, dUs can be neglected. For low test speeds, the change of kinetic energy can also be neglected. In foam tapes, a significant amount of energy can be dissipated by plastic deformation around the crack tip in a direction perpendicular to the surface (see figure 2). The amount of energy depends on the adhesion of the adhesive/tape on the substrate, but also on the foam properties (conformability, ductility). Unfortunately, no analytical approach in this direction was found in the scientific literature.

Figure 2. Local deformation of foam tape at crack tip From a practical point of view, when evaluating the performance of tapes, it is desirable to measure the peel strength values as high as possible. It does no matter if it is the fracture energy only, or if it contains dissipated energy as well. Considering the above, it is clear that there are a number of factors influencing the measured peel strength of a foam tape:

Foams with a high capability to deform in a direction perpendicular to the interface will absorb more energy. The amount of absorbed energy depends on the balance between fracture energy of the adhesive on the substrate and the conformability of the foam.

For thick foams, more plastic energy is dissipated in the foam tape if it is bent backwards in the peel test.

High fracture energy between the adhesive and the substrate is useless if there are other weak factors in the chain; weak foam, weak interface between foam and adhesive or adhesive with poor cohesive strength.

For rough surfaces, softer foams will offer higher peel strength values because they are more conformable and adjusts better to uneven surfaces.

For relatively soft and thick foams, the weight of the roller which is used to fix the tape on the substrate is distributed over a larger area than more rigid and thinner foams. Therefore, the pressure used to fix a soft and/or thick foam tape is lower than for hard and/or thin foams. This effect will be more pronounced for adhesive systems offering only limited fracture energies between adhesive and substrate.

The above considerations also indicate that adhesive failure between substrate and adhesive is not the only possible failure mode. A complete list of failure modes including the indication by what factors they are favored is given in Table 1.

Deformation area Deformation area

• Table 1. Failure modes of double side adhesive coated foam tapes. Failure mode Reason Foam failure Low skin peel strength of foam

Anchorage between adhesive and substrate is the weakest component of the complex

Zip failure Poor adhesive performance, slip-stick crack propagation

Whereas it is clear that the skin peel strength of the foam is a function of the foam density, the absolute value depends on the base-polymer selected for the foam. The absolute level of energy dissipated in the foam also depends on the adhesion between foam and adhesive and on the adhesion level between adhesive and substrate. 1.2. Objective and scope In this study, the peel strength of foam tapes is investigated as a function of numerous parameters:

Substrate (PE, PP, ABS and Stainless Steel) Adhesive (Four solvent borne acrylic and modified acrylic adhesives) Coating weight (65 and 40 g/m2) Polymeric foam (various grades, densities, and thicknesses of polyolefin foams.

The objective of this report is to investigate the behavior of self adhesive tapes based on crosslinked polyolefin foam and solvent borne acrylic pressure sensitive adhesives (psa). The scope of this study is to identify:

Influence of composition, density, and thickness of the foam on tape performance Influence of adhesive composition and formulations on tape performance Interactions between adhesive and foam, influencing the final tape performance

The main evaluation method for this research is the 180 peel strength test (based on AFERA 5001). The foam tapes will be evaluated on PE, PP and ABS after 24 hours ageing and on stainless steel after 1 minute, 20 minutes, and 24 hours ageing. The objective of this technical study is to better understand interactions between foam and adhesive properties. The goal is to develop a design-tool resulting in fast development of foam tapes with the desired performance profile. 2. Materials 2.1. Physically crosslinked polyolefin foam The physically cross-linked polyolefin foam is produced in a three step process (Sekisui process) 1. All ingredients are mixed and extruded into a sheet. 2. The extruded sheet is cross-linked by high voltage electro-beam

• Density

more conformable polymer

more conformable polymer

Con

form

abili

ty

Density

stronger p

olymer

stronger p

olymer

Ski

n pe

el s

treng

th

3. The foaming agent is activated and the sheet is expanded into foam The main variables in this foam manufacturing process are:

Polymer selection Density Thickness

Main foam parameters influencing the tape performance are polymer selection and density. These parameters determine the skin peel strength and the conformability of the foam. The skin peel strength rises with increasing density. The conformability decreases with increasing density. The absolute level and slope of these properties mainly depends on the polymer selection, (example in figure 3 and 4).

Figure 3. Conformability Figure 4. Skin peel strength 2.2. Solvent borne acrylic PSA The solvent borne PSAs are made in two steps. In a first reaction a base polymer is made by radical co-polymerization. In a second step the base polymer is formulated with crosslinker and additives to the final adhesive. The main variables in the adhesive manufacturing process are:

Monomer selection The combination of monomers determines the final Glass Transition Temperature Tg of the polymer/adhesive

Molecular weight and molecular weight distribution The reaction conditions during polymerization but also the choice of initiator and solvents determine the molecular weight and molecular weight distribution of the base polymer. The addition of crosslinker leads to a bonding between polymer chains and forming of a net-work. This can also be seen as an increase of molecular weight.

The main adhesive parameters influencing the tape performance are polymer selection, molecular weight, molecular weight distribution, and modification with additives. These parameters determine the peel properties and the cohesive strength of the adhesive. The peel strength decreases with increasing Tg and decreasing mobility. The cohesive strength rises with increasing molecular weight. The absolute level and slope of these properties mainly depend on the polymer selection and the addition of tackifiers, (example in figure 5 and 6).

• Tg of polymer

Polymer

Polymer + Tackifier

Polymer + Tackifier

Pee

l stre

ngth

Mw of polymer

Polymer

Polymer

+ Tacki

fier

Polymer

+ Tacki

fier

Coh

esiv

e st

reng

th

Figure 5. Influence of Tg on Peel strength Figure 6. Influence of molecular weight on cohesive strength

3. Experimental 3.1. Material selection - Foam The foam has been selected based on the two most important design criteria for tapes: Polymer selection

LDPE based foam EVA based foam

Density

50 - 330 kg/m3 The foam surface is treated in order to increase the surface energy and improve the anchorage with the adhesive. 3.2. Material selection - Adhesive The adhesive has been selected based on Tg (monomer composition), molecular weight and modification. Table 2. Adhesive selection Glass Transition temperature Modification Adhesive mobility Adhesive A High No Low Adhesive B Low No Medium Adhesive C High Yes Medium Adhesive D Low Yes High 3.3. Test method The AFERA 5001, 180 peel strength method has been selected for the evaluation of the various tape constructions. The tape was tested on stainless steel, ABS, PP and PE to evaluate the performance on the different substrates. In addition the tapes were tested on stainless steel after 1 minute, 20 minutes and 24 hours to evaluate the peel build-up.

• 180 Peel strength on steel

0

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

Density

180 Peel strength on steel

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A

1 1 1 1 1

[N/2

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m]

PEPPABSSteel

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180 Peel strength on steel

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DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A DUROTAK 180-154A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

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180 Peel strength on steel

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DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

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180 Peel strength on steel

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

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180 Peel strength on steel

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A DUROTAK 180-182A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

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180 Peel strength on steel

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DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

Density

180 Peel strength on steel

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

Density

180 Peel strength on steel

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65 g/m 65 g/m 65 g/m 65 g/m 65 g/m

DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A DUROTAK 180-184A

1 1 1 1 1

[N/2

5 m

m]

PEPPABSSteel

Density

180 Peel strength on steel

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65 g/m 65 g/m...