NOVEL CONCEPTS FOR CLASSIC MATERIALS:
RADIATION CURING OF
ISOPRENE BASED PRESSURE SENSITIVE ADHESIVES |

Anthony J. Berejka
Ionicorp+
Cold Spring Harbor, NY
Dr. Ralph W. Looney
Research Associate
Exxon Chemical Company
|
| ABSTRACT
Feasibility studies indicate that transparent pressure sensitive
adhesives can le developed with a balance of tack and holding power via radiation curing
using judicious compounding of polyisoprene oligomers and hydrogenated polycyclic
tackifiers with an adroit selection of multifunctional acrylates.
HISTORICAL PERSPECTIVE
Classic pressure sensitive adhesive formulations Contain natural
wood derived tackifiers (rosins and polyterpenes) with a natural rubber base. Synthetics
like styrene-butadiene rubber and later styrenated block copolymers have sometimes
displaced or augmented the use of natural rubber. Likewise, synthetic tackiflers, often
based on Ci and other petroleum feed stocks, have been found to be more effective and
often teas costly than natural products.
Beginning in the 1960's, specialized synthetic polymers based on
acrylate polymerization began to emerge. Here pressure sensitive properties like tack and
hold were achieved through careful monomer selection and polymertitation techniques.
Molecular weight, alkyl chain length, co-monomer selection, all had to be carefully
balanced in order to achieve desired pressure sensitive properties. Acrylate technology
has also led to the more recent use of acrylate terminated oligomers to produce radiation
curable pressure sensitives. For example, acrylate terminated low molecular weight
polyesters, with reactive terminal vinyl functionality, when cured, have shown acceptable
balances of properties.
IRRADIATION CURING
Irradiation curing is a widely accepted industrial technique used
extensively in the graphic arts and converting areas. Ultra-violet light or low voltage
electron beams are used to cure (crosslink) or "dry" liquid systems, like inks
or coatings, which have no hydrocarbon solvent or water as a vehicle. Excellent
performance properties, like hardness, gloss or release, can be achieved, depending upon
the application. With both ultra-violet irradiators and low voltage electron beams, these
properties are attained at relatively low exposure or dose levels. This then implies high
production throughout.
The ecological advantages of attaining not Just low volatile emissions,
but practically no volatile emissions, make radiation curing an excellent process
technique for our current environment. Energy savings, enhanced product quality, new
product capabilities and the ability to cure materials on thermally sensitive substrates
are proven pluses for irradiation processing.
Ultra-violet irradiators and low voltage electron beam accelerators are
available from numerous reputable suppliers. Electron beams offer higher through-put
capacity, but require a higher capital investment cost. All this equipment has a proven
record of industrial safety. Oft times, irradiation curing equipment can be retrofitted
onto existing converting lines. The line space needed for either ultra-violet or electron
beam processors is significantly less, by almost orders of magnitude, than the space
required for older thermal curing or drying ovens.
In summary radiation curing offers:
 | High product out-put.
|
 | No volatile emissions.
|
 | low temperature processing.
|
 | Savings on plant floor space.
|
 | Energy savings.
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 | Enhanced product quality.
|
 | Reliability and safety.
|
 | New product capabilities.
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 | Cost effectiveness.
|
METHODS OF TEST
Pressure sensitive adhesives produced via more traditional or by
radiation curing techniques can be characterized by a number of industry standard test
procedures. For example, resistance -to-peel is a complex test involving backing modulus
or flexibility as well as the rheological properties of the adhesive mass in addition to
various interfacial interactions. Some skilled in the art tend to allow destructive test
results, like resistance-to-peel to fall where they may in favor of more meaningful bond
durability tests and bond formation tests like tack.
Of the variety of tack tests, rolling ball tack (ASTM-3121/PSTC-6) is
probably the more discriminating. Statistically designed experiments have shown other tack
tests, like probe techniques and loop or quick stick methods, to often be related to the
complex resistance-to-peel measurements as shown through high coefficients of correlation.
The rolling ball, for its simplicity, is quite able to differentiate between the common
understanding of tack and materials which exhibits harsh or raspy pressure Sensitive
quality.
With pressure sensitives, bond durability is in most cases related to
the adhesives' resistance to creep. Here again, a simple traditional method of suspending
a weight from a pressure sensitive coated material, wherein the adhesive is adhered to a
stainless steel plate, using a controlled contact area, isa good indication of creep
resistance. Published results have yet to correlate sophisticated viscoelastic
measurements with creep results obtained via vertical hold tests ~TC-7). More demanding in
such hold tests is to measure the time a given weight can be supported rather than just
the first indications of slippage.
EXPERIMENTAL TECHNIQUES
100% solids mixtures of isoprene oligomers (e.g. Hardman Isolene
400) with tackifylng resins were prepared in a slightly heated kneader mixer, with
sufficient heat and shear being used so as to flux the tackifier into the polyisoprene. To
attain transparency hydrogenated polycyclic tackifiers were preferred (e.g. Exxon
Chemical's Escarez 5380). Subsequent to preparing these blends, different
multifunctional acrylate monomers were added at different quantities.
Hand draw downs were made using a Bird applicator to achieve adhesive
costing thickness of approximately 50 microns (about 2 miss) Onto 37 micron (1.5 mil)
polyester film. These 100% non-volatile pressure sensitive coatings were then subjected to
an irradiation source. All of the electron beam irradiation was done using an Energy Sciences
Electrocurtain at 250 KeV with the beam current and sample transport speed being
adjusted in order to achieve a desired level of dose or beam exposure. Dose is the
electron beam energy imparted to the sample and is often expressed in megarads (Mrad)
wherein one megarad equals 10 ergs per gram. The under beam atmosphere was adjusted to
permit either atmospheric air to be present or to have the air purged and the irradiation
to take place in a nitrogen atmosphere.
After being transported in contact with a release film, the test
samples were subjected to the rolling ball tack test (ASTM D31-/PSTC-6) and a vertical
hold test (modified PSTC-7). In the tack test, the ball roll was recorded in centimeters.
For the hold test, a 2.54 by 2.54 centimeter ~ inch by 1 inch) contact area of adhesive to
stainless steel plate was used. The time over which either a 500 gram or a 1000 gram
weight could be suspended by the adhesive mass was recorded.
FORMULATION MATERIALS
Two different molecular weight versions of polyisoprene oligomers
derived by the depolymerization of synthetic polyisoprene by Hardman Incorporated (13ellevilie,
NJ) were examined: |
|
| |
ISOLENE 40 |
ISOLENE 400 |
Molecular Weight by GPC: |
40,000 |
90,000 |
Viscosity, poises at 38°C: |
360-550 |
3,000-5,000 |
Unsaturation, mole %: |
92% |
92% |
Specific Gravity at 25°C: |
0.92 |
0.92 |
| In addition, a cursory look was given to the possible contribution a low
molecular weight 1,2cis polybutadiene oligomer could make in these systems. Ricon 154 from
Colorado Chemical (Broomfield, CO) was used in this regard: |
|
| |
RICON 154 |
| Molecular weight by GPC: |
3,200 |
| Viscosity, poises at 450C: |
2,500 |
| 1-2 vinyl content. mole %: |
90% |
| Specific Gravity at 250C: |
0.92 |
Despite the high degree of pendant vinyl functionality in this
polybutadiene oligomer, by itself it is only moderately responsive to irradiation
crosslinking since for every pendant vinyl group there is also a chain stopping tertiary
hydrogen. The chemical Structures for both these polyisoprenes and this polybutadiene
oligomer are:
(to view structures click on link)
POLYISOPRENE
1/2 - POLYBUTADIENE
The tackifier of choice was the lowest softening point grade of a
homologous series of hydrogenated or saturated polycyclic hydrocarbons. These water white
tackifying resins are produced by the Exxon Chemical Company. The different grades
in this series are: |
|
| |
Escorez |
Escorez |
Escorez |
Escorez |
| |
5380 |
5300 |
5320 |
5340 |
| Softening point, R&B, °C: |
85 |
105 |
125 |
140 |
| Gardner color: |
<1 |
<1 |
<1 |
<1 |
| Bromine number (c gm/gm): |
2 |
2 |
2 |
2 |
| Viscosity, poises at 150°C: |
4 |
20 |
220 |
350 |
| As will be shown in the data below, a blend of two
different multifunctional acrylates was used to enhance the radiation cure rate. Initial
experiments were conducted using difuncitional acrylates with alkyl mid-sections in order
to promote the compatibility of the acrylate monomer with the very non-polar isoprene
oligomer and tackifier blends. The high degree of polarity of the commonly used
trimethyloipropane triacrylate by itself led to phase separation and cloudiness when
incorporated into these transparent and highly non-polar systems.
The high alkyl difunctional monomers examined were: 1/6-hexanediol
diacrylate, SR-238 from Sartomer Company, Inc. (Exton, PA) and a difunctional monomer with
a long alkyl mid-section of about C15 in length, Sartomer's SR-2000. Of these
the SR-2000 exhibited a higher degree of compatibility and no cloudiness in the mixtures
studied. Both of these monomers moreover could enhance the compatibility of the more
reactive trimethyloipropane triacrylate, Sartomer's SR-351.
(to view structures click on link)
1,6-HEXANEDIOL
DIACRYLATE
HIGH ALKYL MID-SECTION DIACRYLATE
TRIMETHYLOPROPANE TRIACRYLATE
Finally, an experiment was conducted to see if the most promising at
these isoprene oligomer systems could also be photoinitiated under ultra-violet light.
Using Ciba-Geigy's (Oak Brook, IL) liquid photoinitiator, Irgacure 500, a 50/50
mixture by weight of 1-hydroxyceclohexylphenylketone and benzophenone, at 6% by weight,
some encouraging results were obtained with the tack and bold properties similar to those
noted for electron beam cured systems. The desired transparency and clarity were also
maintained.
EXPERIMENTAL DATA
2:1 blend ratios of the higher molecular weight isoprene oligomer
to the Escorez 5380 tackifier were studied using the two alkyl mid-section difunctional
acrylates at approximately the Same molar concentrations. In these systems, moderately
high electron beam exposure levels of 10 to 15 Mrads were required in order to develop any
cohesive strength as measured by creep resistance in the vertical hold test These
materials were all irradiated in air. |
|
| Isolene 400 |
66.7 |
66.7 |
63.3 |
64.1 |
| Escorez 5380 |
33.3 |
33.3 |
31.6 |
32.1 |
| SR-238, HDODA |
-- |
-- |
5.1 |
-- |
| SR-2000 |
-- |
-- |
-- |
3.8 |
| EB dose, Mrads: |
5 |
10 |
10 |
15 |
| Rolling ball tack. cm: |
2.4 |
2.2 |
1.7 |
1.9 |
| 178° hold, min.(l"x1"x500g) |
1.2 |
3.0 |
250 |
1860 |
By shifting to a 1:1 isoprene oligomer to tackifying
resin blend ratio and to the more commonly used TMPTA, again at comparable molar
concentrations with respect to the unsaturated polyisoprene, more encouraging holding
power results were obtained at moderate electron beam dose levels. Unfortunately, because
of their incompatibility, these blends had to be remixed just prior to coating in order to
redisperse the TMP'TA into the pressure sensitive system. Again all the irradiation was
carried out in air.
With these compounds, one would have expected a tighter crosslinked
system from the higher isoprene level and thus a higher resistance to creep. Surprisingly,
the 1:1 ratio of the isoprene oligomer to tackifer gave both good creep resistance and
maintained satisfactory rolling ball tack compared to the 2:1 blend ratio at this same
dose. |
|
| Isolene 400 |
50.0 |
47.6 |
67.3 |
62.6 |
| Escorez 5380 |
50.0 |
47.6 |
33.3 |
31.3 |
| SR-351, TMPTA |
-- |
4.8 |
-- |
6.2 |
| EB dose, Mrads: |
10 |
10 |
10 |
10 |
| Rolling ball tack. cm: |
1.7 |
9.3 |
0.4 |
0.5 |
| 178° hold, min.(l"x1"x500g) |
2.Oc |
> 1440 |
l.0c |
95c |
| If one replaces half of the isoprene oligomer, in the 2:1 elastomeric
oligomer to tackfier blend with another unsaturated reactive oligomer, 1,2-polybutadiene,
there is a significant increase in holding power, but a complete loss of tack as measured
by the rolling ball test. Again the irradiation was done in air. |
|
| Isolene 400 |
67.3 |
62.6 |
33.3 |
32.3 |
| Ricon 154 |
-- |
-- |
33.3 |
32.3 |
| Escorez 5380 |
33.3 |
31.3 |
33.3 |
32.3 |
| SR-351, TMPTA |
-- |
6.2 |
-- |
3.2 |
| EB dose, Mrads: |
10 |
10 |
10 |
10 |
| Rolling ball tack. cm: |
0.4 |
0.5 |
2.3 |
>15 |
| 178° hold, min.(l"x1"x500g) |
1 .0c |
95c |
3.Oc |
> 1440 |
| A common technique in the radiation curing industry is to provide an
inert atmosphere under the irradiation source. This can be obtained by purging the air and
replacing it with a nitrogen blanket. This is often done to reduce the oxygen inhibition
which retards the cure rate of many irradiation curable systems. Each particular system
may respond somewhat differently In the data below, one of the 1~ isoprene to Escorex 5380
systems showed almost no change in properties. However, a blend containing but 24%
1,2~polybutadiene showed a much tighter cure under nitrogen than in air, all being exposed
to the same dose level. |
|
| Isolene 400 |
47.6 |
47.6 |
47.6 |
47.6 |
| Ricon 154 |
-- |
-- |
23.8 |
23.8 |
| Escorez 5380 |
47.6 |
47.6 |
23.8 |
23.8 |
| SR-351, TMPTA |
4.8 |
4.8 |
4.8 |
4.8 |
| EB dose, Mrads: |
10 |
10 |
10 |
10 |
| Atmosphere: |
air |
N2 |
air |
N2 |
| Rolling ball tack. cm: |
9.3 |
1.7 |
0.1 |
>15 |
| 178° hold, min.(l"x1"x500g) |
> 1440 |
> 1440 |
14c |
> 1440 |
| Increasing the concentration of a multifunctional monomer can also be
used to enhance cure rate. However, as noted above, the widely used trimethylolpropane
triacrylate is not that compatible with these very non-polar systems. The data below show
how rolling ball tack becomes worse as the TM~~A concentration increases, possibly due to
some phase separation before curing. |
|
| Isolene 400 |
47.6 |
46.5 |
45.5 |
| Escorez 5380 |
47.6 |
46.5 |
45.5 |
| SR-351, TMPTA |
4.8 |
7.0 |
9.1 |
| EB dose, Mrads: |
10 |
10 |
10 |
| Atmosphere: |
N2 |
N2 |
N2 |
| Rolling ball tack. cm: |
1.7 |
12.5 |
>15 |
| While the difunctional acrylates with alkyl mid-sections were not that
effective in promoting a balance of tack and hold at moderate electron beam doses of 10
Mrads, their compatibility with the non-polar isoprene oligamer and polycyclic tackifier
blends was used to enhance the compatibility of the more reactive TMPTA. Thus, blends of
TMPTA and the high alkyl diacrylate with a C15 mid-section were evaluated. The
compatibility of this diacrylate with the olefinic oligomer and the cydoaliphatic
tackifier also makes it a good diluent. These systems based on multifunctional acrylate
blends showed good shelf stability over several weeks with no need to remix them just
prior to coating. The lower molecular weight isoprene oligomer, Isolene 40, exhibits
significantly lower viscosity but preliminary indications show that It may be difficult to
useIhis grade to achieve a desired balance of tack and hold. Perhaps, the molecular weight
between crosslinks is too low for this desired balance. |
|
| Isolene 40 |
45.5 |
45.5 |
| Escorez 5380 |
45.5 |
45.5 |
| SR-351, TMPTA |
4.5 |
4.5 |
| SR-2000 |
4.5 |
4.5 |
| EB dose, Mrads: |
5 |
2.5 |
| Atmosphere: |
N2 |
N2 |
| Rolling ball tack. cm: |
> 15 |
8.2 |
| 178° hold, min.(l"x1"x500g) |
> 1440 |
15c |
| Another experiment confirmed the merits of using the multifunctional
acrylate blends. Some of these results also confirmed the previously noted poor holding
properties exhibited by the systems containing only the compatible difunctional acrylate. |
|
| Isolene 400 |
45.5 |
47.7 |
45.5 |
47.7 |
| Escorez 5380 |
45.5 |
47.7 |
45.5 |
47.7 |
| SR-351, TMPTA |
4.5 |
2.3 |
-- |
-- |
| SR-2000 |
4.5 |
2.3 |
9.0 |
4.6 |
| EB dose, Mrads: |
5 |
5 |
5 |
5 |
| Atmosphere: |
N2 |
N2 |
N2 |
N2 |
| Rolling ball tack. cm: |
4.9 |
2.1 |
2.7 |
4.3 |
| 178° hold, min.(l" x 1" x 500g) |
> 1440 |
> 1440 |
6c |
4c |
| 178° hold, min.(l" x 1" x 1000g) |
> 1440 |
445a |
|
|
The 1:1 blends of the polyisoprene oligomer (Isolene
400) and the hydrogenated polycyclic tackifier (Escorez 5380) when used with the
multifunctional monomer blend (Sartomer SR-351 and SR-2000) and cured via an electron beam
in an inert nitrogen atmosphere with doses or energy input as low as 3 Mrads yielded
commercially acceptable transparent pressure sensitive adhesives.
Duplicate experiments showed that consistent results could be achieved
with this approach. |
|
| Isolene 400 |
45.5 |
45.5 |
47.7 |
47.7 |
| Escorez 5380 |
45.5 |
45.5 |
47.7 |
47.7 |
| SR-351, TMPTA |
4.5 |
4.5 |
2.3 |
2.3 |
| SR-2000 |
4.5 |
4.5 |
2.3 |
2.3 |
| EB dose, Mrads: |
3 |
3 |
1 |
1 |
| Atmosphere: |
N2 |
N2 |
N2 |
N2 |
| Rolling ball tack. cm: |
5.5 |
2.4 |
0.6 |
0.6 |
| 178° hold, min.(l" x 1" x 500g) |
> 1440 |
> 1440 |
48c |
2c |
| 178° hold, min.(l" x 1" x 1000g) |
> 1440 |
345a |
|
|
MARKET POTENTIAL
Through judicious compounding, pressure sensitive adhesives based on
100% solids, non-volatile components can be irradiation cured to yield transparent
adhesives which exhibit reasonable commercially acceptable properties. These properties
can be achieved using the efficient electron beam process at commercially acceptable dose
exposure. Because of their non-polar make-up, these adhesives could find application where
existing irradiation curable pressure sensitives based on polar backbones have experienced
some market difficulties. Non-polar materials like these exhibit electrical insulating
properties and resistance to polar solvents and water.
These feasibility studies have merely pointed out that when properly
compounded, classic materials, like polyisoprene (in this case in a low molecular weight
form) can yield pressure sensitive adhesives with reasonable balances of tack and hold.
Hopefully, formulators will be able to take advantage of these feasibility studies to
generate industrially viable products. Such products can be made using the efficient and
cost-effective irradiation curing process. Again, with the proper selection of initiators,
these systems should also respond to ultra-violet irradiation curing.
FORMULATING OLIGOMERIC MATERIALS
When formulating oligomeric materials for irradiation curing, some
general guidelines ought be kept in mind in order to achieve a desired balance of
properties. |
|
PROPERTY TRADE-OFFS AND BALANCES |
Physical Properly |
Network Parameter |
Formulation Options |
Fluidity |
 | Low Molecular Weight, Mn
|
|
 | Use Low Molecular Weight Oligorners
|
 | Increase Diluents
|
|
| |
|
Elongation and Law Shrinkage |
 | High Molecular Weight Between Crosslinks, Mc
|
 | Low Functionality
|
|
 | Use High Molecular Weight Oligomers
|
 | Use Di-Functional Crosslink Additives
|
|
| |
Tensile Strength |
 | High Molecular Weight, Mn
|
 | High Functionality
|
|
 | Use High Molecular Weight Oligomers
|
 | Use Tri-Functional Crossink Additives
|
|
| |
Cure Rate |
 | High Functionality
|
|
 | Use Low Molecular Weight Oligomers
|
 | Use Muiti-Functional Crosslink Additives
|
 | Use Diluent Monomers
|
|
| |
|
| |
|
In compounded pressure sensitives, the development of
some properties, like tack, often require some lower molecular weight species, such as
tackifier resins. In contrast, creep resistance can be obtained through the use of higher
molecular weight materials and through the build up of crosslinks between high polymer
chains. Resistance-to-peel often relies on attaining a balance of relatively high tensile
properties and high elongation in the final pressure sensitive in order to both enhance
the contact area under the nib and at the same time give the adhesive sufficient integrity
to be cohesive. In cured pressure sensitives based on oligomeric materials, reflection on
the need to achieve a controlled molecular weight between crosslinks would indicate how
such balances of properties can be attained.
Wheras, most materials made for irradiation curing are based on
sophisticated synthesized oligomers, the intermediate level properties obtained via these
formulated materials have relatively low raw material costs. The exemplar formula based on
a 1:1 isoprene oligomer to polycyclic tackifier and 9% of an equal blend of the two select
monomers has a relatively moderate raw materials cost To this mixing and compounding costs
would also have to be added. Because of the viscosity of the base isoprene oligomer, some
modest heating will also likely be needed to attain high speed smooth coatings.
ACKNOWLEDGEMENTS AND RECOGNITION
This paper is dedicated to the memory of Dr. Ralph Looney whose
untimely passing away in the spring of 1986 left many of the goals and ambitions of this
program unfulfilled. Dr. Looney, if he were alive, and Mr. Berejka would like to
acknowledge the support and encouragement of Dr. Joseph A. Mountain, Manager of Project
Development, Adhesives and Sealants Market Sector, Exxon Chemical Company, Houston, Texas.
Dr. Mountain recognized the potential for this program in the pressure sensitive adhesives
market.
Dr. Ralph Looney was a Research Associate with Exxon Chemical Company
in the polymer and specialty chemical field. Ralph was with Exxon for more than twenty
years.
Anthony Berejka is an independent consultant experienced in the
pressure Sensitive adhesive area and has done extensive work in the field of irradiation
processing and technology. He is President of Ionicorp+, a consulting firm, Post Office
Box 79, Cold Spring Harbor, New York 11724. |
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