U.S. patent application number 11/083222 was filed with the patent office on 2005-07-21 for longitudinal shrink films.
This patent application is currently assigned to PLASTIC SUPPLIERS, INC.. Invention is credited to Vynckier, Denis Leon.
Application Number | 20050158492 11/083222 |
Document ID | / |
Family ID | 32869329 |
Filed Date | 2005-07-21 |
United States Patent
Application |
20050158492 |
Kind Code |
A1 |
Vynckier, Denis Leon |
July 21, 2005 |
Longitudinal shrink films
Abstract
A heat-shrinkable film and a method of its manufacture are
provided. In an exemplary embodiment, a polystyrene film exhibits
heat-induced growth in the cross direction of great than or equal
to 5% with greater than or equal to 30% concomitant shrinkage in
the machine direction. The films may comprise crystal polystyrene,
high impact polystyrene, and/or elastomers. A method of manufacture
is disclosed which includes a post-extrusion temperature
conditioning step.
Inventors: |
Vynckier, Denis Leon;
(Deinze, BE) |
Correspondence
Address: |
KATTEN MUCHIN ROSENMAN LLP
525 WEST MONROE STREET
CHICAGO
IL
60661-3693
US
|
Assignee: |
PLASTIC SUPPLIERS, INC.
Columbus
OH
|
Family ID: |
32869329 |
Appl. No.: |
11/083222 |
Filed: |
March 18, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11083222 |
Mar 18, 2005 |
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10771346 |
Feb 5, 2004 |
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6897260 |
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60445272 |
Feb 6, 2003 |
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Current U.S.
Class: |
428/34.9 |
Current CPC
Class: |
C08J 5/18 20130101; B29K
2105/0088 20130101; B29C 55/28 20130101; B29C 61/003 20130101; Y10T
428/1328 20150115; B29C 55/04 20130101; Y10T 428/1352 20150115;
B29K 2025/00 20130101; C08J 2325/04 20130101 |
Class at
Publication: |
428/034.9 |
International
Class: |
F16B 004/00; B65B
053/00 |
Claims
1-12. (canceled)
13. A packaged good comprising a consumable item and a heat treated
film wrapped around at least a portion of the consumable item,
which heat treated film is obtained by exposing to heat a shrink
film comprised of a polystyrene polymer blend which exhibits
shrinkage in the length direction and controlled growth in the
cross direction upon exposure to heat.
14. The packaged good of claim 13 in which the consumable item
includes batteries, cans, bottles, disposable lighters, pens and
decorative items.
15. The packaged good of claim 13 in which the consumable item is a
battery.
16. The packaged good of claim 13 in which the heat treated film
forms a perforated or non-perforated neck band around the
consumable item.
17. The packaged good of claim 13 in which the heat treated film is
clear, matte, translucent, or opaque.
18. The packaged good of claim 13 in which the heat treated film
includes a packaging label.
19. The packaged good of claim 18 in which the packaging label is
printed onto the film.
20.-41. (canceled)
Description
[0001] This application claims priority to the provisional U.S.
patent application entitled, Polystyrene Longitudinal Shrink Films,
filed Feb. 6, 2003, having a Ser. No. 60/445,272, the disclosure of
which is hereby incorporated in its entirety by reference.
FIELD OF THE INVENTION
[0002] The present invention relates generally to heat-shrinkable
film. More particularly, the present invention relates to
heat-shrinkable polystyrene films that exhibit temperature
dependent shrinkage in one direction with concomitant expansion in
another.
BACKGROUND OF THE INVENTION
[0003] Heat-shrinkable films have widely been used for various
industrial applications, for example, such as with shrink-wrap
films, shrinkable labels and cap seals, by making use of their
property of heat-dependent shrinkage. The films have been applied
to a variety of surfaces, including plastic and glass surfaces.
Shrink films have been manufactured from vinyl chloride resins,
polystyrene resins or polyester resins; however, in many instances,
film shrinkage is concomitant with undesirable curling of the outer
edges of the film. The undesirable curling of the outer edges has
limited the application of shrink films. Therefore, there is a need
for shrink films that have little to no curling.
SUMMARY OF THE INVENTION
[0004] The foregoing needs are met, to an extent, by the present
invention, wherein in one aspect shrink film is provided comprised
of a polystyrene polymer blend which, upon exposure to heat,
exhibits shrinkage in the length direction and controlled growth in
the cross direction, thus allowing the film to exhibit reduced
curling of its outer edges as the film shrinks upon exposure to
heat. The shrink film may exhibit shrinkage in the length direction
in the range of about 10% to about 90% and exhibit a shrinkage in
the cross direction in the range of about 30% to about -30% (a
negative value indicates growth) when subjected to heat in a hot
air oven at 120.degree. C. after about five minutes. In some
embodiments, the shrink film may exhibit shrinkage in the length
direction of about 50% and exhibit shrinkage in the cross direction
of about -10% (a negative value indicates growth) when subjected to
heat in a hot air oven at 120.degree. C. after about five minutes.
In other embodiments, the shrink film may exhibit shrinkage in the
length direction of about 30% and exhibit a shrinkage in the cross
direction of about -5% (a negative value indicates growth) when
subjected to heat in a hot air oven at 120.degree. C. after about
five minutes. In still yet other embodiments, the shrink film may
exhibit shrinkage in the length direction of up to about 50% or
greater and exhibit a shrinkage in the cross direction of up to
about -10% (a negative value indicates growth) when subjected to
heat in a hot air oven over a temperature range of about
220.degree. F. to about 250.degree. F. after about five minutes.
The polystyrene polymer blend includes crystal polystyrene and
elastomers, high impact polystyrene and elastomers, and/or crystal
polystyrene, high impact polystyrene and elastomers. The
polystyrene polymer blend may include 48 parts crystal polystyrene,
2 parts high impact polystyrene and 50 parts elastomers. In other
embodiments, polystyrene polymer blends include 33 parts crystal
polystyrene, 2 parts high impact polystyrene and 65 parts
elastomers. In yet other embodiments, polystyrene polymer blends
include 68 parts crystal polystyrene, 2 parts high impact
polystyrene and 30 parts elastomers.
[0005] In accordance with another embodiment of the present
invention, a packaged good is provided comprising a consumable item
and a heat treated film wrapped around at least a portion of the
consumable item, which heat treated film is obtained by exposing to
heat a shrink film comprised of a polystyrene polymer blend which
exhibits shrinkage in the length direction and controlled growth in
the cross direction upon exposure to heat. The packaged good may be
a consumable item including batteries, cans, bottles, disposable
lighters, pens and decorative items. The film may form a perforated
or non-perforated neck band around the consumable item and may be
clear, matte, translucent, or opaque. The packaged good with the
heat treated film may include a packaging label and the label may
be printed onto the film.
[0006] In yet another embodiment of the present invention, a method
of making a shrink film comprising (a) providing pellets of a
polystyrene polymer blend, (b) drying the pellets, (c) melting the
pellets to form a molten mass at a desired viscosity value or range
of values, (d) increasing the viscosity of the molten mass, (e)
stretching the resulting molten mass to form a film, and (f)
annealing the resulting film. The drying step of the method may be
carried out in an air dryer. The melting step may be carried out at
a temperature range of about 150.degree. C. to about 300.degree.
C., about 180.degree. C. to about 270.degree. C., or at a
temperature of about 200.degree. C. The first viscosity may range
from about 3,000 P to about 6,000 P, about 4,000 P to about 5,000
P, or be about 4,500 P, at about 240.degree. C. and an apparent
shear rate of about 55 seconds.sup.-1. The second viscosity may
range from about 16,000 P to about 19,500 P, about 16,500 P to
about 18,000 P, or be about 17,500 P, at about 180.degree. C. and
an apparent shear rate of about 55 seconds.sup.-1. The viscosity
increasing step may be carried out in a polymer cooling unit, and
the unit may be a Koch polymer cooling unit adapted for polystyrene
use. The stretching step of the method may be carried out using a
blown film orientation process. The annealing step of the method
may be carried out at a temperature ranging from about 25.degree.
C. to about 200.degree. C., about 30.degree. C. to about
175.degree. C., about 50.degree. C. to about 100.degree. C., or
about 90.degree. C.
[0007] In still yet another embodiment of the present invention, a
method of increasing the viscosity of a polystyrene polymer blend
suitable for shrink films is provided, comprising (a) providing
pellets of a polystyrene polymer blend, (b) melting the pellets to
form a molten mass at a first desired viscosity value or range of
values, and (c) cooling the molten mass to a second desired
viscosity value in a polymer cooling unit. The melting step may be
carried out at a temperature range of about 150.degree. C. to about
300.degree. C., about 180.degree. C. to about 270.degree. C., or at
a temperature of about 200.degree. C. The first viscosity may range
from about 3,000 P to about 6,000 P, about 4,000 P to about 5,000
P, or be about 4,500 P, at about 240.degree. C. and an apparent
shear rate of about 55 seconds.sup.-1. The second viscosity may
range from about 16,000 P to about 19,500 P, about 16,500 P to
about 18,000 P, or be about 17,500 P, at about 180.degree. C. and
an apparent shear rate of about 55 seconds.sup.-1. The viscosity
increasing step may be carried out in a polymer cooling unit, and
the unit may be a Koch polymer cooling unit adapted for polystyrene
use. The second viscosity may range from about two times to about
ten times, about four times to about eight times, or about six
times that of the first viscosity value.
[0008] There has thus been outlined, rather broadly, certain
embodiments of the invention in order that the detailed description
thereof herein may be better understood, and in order that the
present contribution to the art may be better appreciated. There
are, of course, additional embodiments of the invention that will
be described below and which will form the subject matter of the
claims appended hereto.
[0009] In this respect, before explaining at least one embodiment
of the invention in detail, it is to be understood that the
invention is not limited in its application to the details of
construction and to the arrangements of the components set forth in
the following description or illustrated in the drawings. The
invention is capable of embodiments in addition to those described
and of being practiced and carried out in various ways. Also, it is
to be understood that the phraseology and terminology employed
herein, as well as the abstract, are for the purpose of description
and should not be regarded as limiting.
[0010] As such, those skilled in the art will appreciate that the
conception upon which this disclosure is based may readily be
utilized as a basis for the designing of other structures, methods
and systems for carrying out the several purposes of the present
invention. It is important, therefore, that the claims be regarded
as including such equivalent constructions insofar as they do not
depart from the spirit and scope of the present invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] FIG. 1 is a graph depicting the percent shrinkage of a
POLYFLEX LMOPS 120 Gauge film of the present invention at a given
temperature for five minutes. The solid line represents shrinkage
in the length direction and the dotted line represents expansion in
the cross direction.
[0012] FIG. 2 is a graph depicting the percent shrinkage of a
POLYFLEX LMOPS 160 Gauge film of the present invention at a given
temperature for five minutes. The solid line represents shrinkage
in the length direction and the dotted line represents expansion in
the cross direction.
[0013] FIG. 3 is a graph depicting the percent shrinkage of a
POLYFLEX LMOPS 200 Gauge film of the present invention at a given
temperature for five minutes. The solid line represents shrinkage
in the length direction and the dotted line represents expansion in
the cross direction.
DETAILED DESCRIPTION
[0014] In one embodiment of the instant invention, plastic films
and a method of their manufacture are described. The polymer films
are generated that, when heat treated, shrink in the machine
direction and expand in the cross direction. This shrinkage and
expansion may occur simultaneously. The machine direction will be
defined herein as the "longitudinal" or "length" direction. The
"cross direction" or "cross web direction" will be defined herein
as the direction perpendicular to the machine direction.
Embodiments of films described herein exhibit reduced edge-curling
characteristics and can be produced in clear, matte, translucent
colors and opaque colors. Films of the present invention may be
suitable for back side and/or front side printing.
[0015] Films of the present invention may comprise various polymers
and polymer grades known in the art. Preferably, in some
embodiments, polymers are selected that, when used alone or in a
blend, enable "memory" to be stored from an orienting process
described herein. Many of the determinants for polymer selection
are known to one or ordinary skill in the art and/or will be
apparent from the teachings herein. For example, where high
temperature processing is desired, polymers with higher softening
points may be selected, such as, for example, high molecular weight
polymers.
[0016] Polymer classes that may be suited for the present
invention, include, but are not limited to, crystal polystyrene,
high impact polystyrene, and elastomers. In each of the
aforementioned classes, various grades of the respective polymers
are also included.
[0017] Crystal polystyrene is a polymer that can provide stiffness,
heat resistance, gloss, and clarity (for clear films). All grades
may be used in the present invention; however a melt flow of about
2 and a molecular weight of 350,000 (wt. avg.) is preferred.
Preferred characteristics of crystal polystyrene may include a melt
flow that ranges from about 0.7 to about 40 (ASTM D-1238G). The
molecular weight (Weight Average) preferably ranges from 180,000 to
475,000 (ASTM D-3593), and more preferably ranges from 300,000 to
350,000, and even more preferably is 350,000. The term "about" has
been incorporated herein to account, for example, for the
inaccuracies inherent and present in such measurements known in the
art.
[0018] High impact polystyrene polymers can provide slip
(anti-blocking) and anti-scratching characteristics, and all grades
can be used in the present invention. These polymers comprise a
combination of crystal polystyrene and butadiene rubber particles.
Rubber particle sizes may range from about 1 micron to about 10
microns (high impact only), and preferably about 3 to about 4
microns in some embodiments. Without being limited to or bound by
theory, it is thought that the rubber blooms to the surface during
orienting which aids in creating a void between film layers. The
void, comprising an air pocket between film layers, is one factor
in determining anti-blocking and anti-scratching characteristics of
the film.
[0019] High impact polystyrene may have a melt flow that ranges
from about 0.7 to about 40 (ASTM D-1238G), and preferably a melt
flow of about 2.0. The molecular weight (Weight Average) of the
polymers may range from 180,000 to 475,000 (ASTM D-3593), more
preferably between 300,000 to 350,000, and even more preferably is
350,000.
[0020] Synthetic polymers (also known as "elastomers") are thought
to provide strength, flexibility and may be a significant component
in storing the shrink memory. Synthetic polymers are known in the
art, and commonly supplied as a blend of a synthetic rubber and a
"carrier resin." The carrier resin is often crystal polystyrene,
high impact polystyrene, or a combination thereof, but may comprise
other polymers as well. Synthetic rubbers that may be used in some
embodiments of the current invention include, but are not limited
to, styrene isoprene styrene (SIS), styrene butadiene styrene
(SBS), and styrene butadiene--also known as SB block copolymer. All
grades can be used, including branched or linear molecular
structures.
[0021] For certain applications, synthetic polymers are commonly
supplied in the art as 75% of a carrier resin and 25% of a
synthetic rubber, which is the maximum amount of synthetic rubber
that may be used and still meet FDA compliance 21 CFR 177.1810.
However, other formulations are available, both with more or less
synthetic rubber, and various types and grades of synthetic rubbers
are also available and may be incorporated in the invention.
[0022] Synthetic polymers in some embodiments may have a melt flow
that ranges from about 0.7 to about 40 (ASTM D-1238G), and more
preferably about 8.0. The molecular weight (Weight Average) of the
polymers may range from 100,000 to 500,000 (ASTM D-3593), and more
preferably is 250,000.
[0023] In some embodiments, polymers for films may be selected from
one, two or each of three groups mentioned and combined to create
blended polymer films. Table 1 provides a listing of formulations
that may be suitable in the preparation of films of the present
invention. For clarity in description, a skilled artisan should
appreciate from the teachings herein that the percent of crystal
polystyrene and the percent of butadiene in "high impact
polystyrene" have not been listed. However, it should be
appreciated that high impact polystyrene is a combination of the
two polymers, and for the first 17 formulations, "high impact
polystyrene" is, in fact, about 92% crystal polystyrene and about
8% butadiene.
[0024] Similarly, elastomers are commercially available as a
combination of a carrier resin and a synthetic rubber. Column 4
lists the percentage of "elastomer", where the elastomer comprises
75% crystal polystyrene and 25% synthetic rubber. Column 5 provides
the net synthetic rubber in the composition in the complete
formulation.
1TABLE 1 Polymer Formulations Formulation Crystal Elastomer/ Net
Synthetic No PS HIPS Synthetic Polymer Rubber 1) 68% 2% 30% 7.50%
2) 63% 2% 35% 8.75% 3) 58% 2% 40% 10% 4) 53% 2% 45% 11.25% 5) 48%
2% 50% 12.50% 6) 47% 3% 50% 12.50% 7) 49% 1% 50% 12.50% 8) 43% 2%
55% 13.75% 9) 38% 2% 60% 15% 10) 33% 2% 65% 16.25% 11) 34% 1% 65%
16.25% 12) 28% 2% 70% 17.50% 13) 23% 2% 75% 18.75% 14) 24% 1% 75%
18.75% 15) 18% 2% 80% 20% 16) 13% 2% 85% 21.25% 17) 14% 1% 85%
21.25% 18) 0% 100% 0% 0% 19) 0% 95% 5% 1.25% 20) 0% 90% 10% 2.50%
21) 0% 85% 15% 3.75% 22) 30% 60% 10% 2.50% 23) 15% 50% 35% 8.75%
24) 50% 30% 20% 5% 25) 60% 20% 20% 5% 26) 25% 15% 60% 15% 27) 20%
10% 70% 17.50% 28) 10% 10% 80% 20% 29) 10% 5% 85% 21.25%
[0025] The blends in Table 1 may be chosen or prepared to create
the "feel" or flexibility of the film to match an end use
application. In the formulations in Table 1, increasing the net
synthetic rubber in a given composition may increase the
flexibility of the film, such that films of the first formulations
are not as ductile as the seventeenth. Also, films prepared from
formulations 18-21 are considered "semi-clear" by virtue of their
high butadiene content.
[0026] Where all other processing parameters are equal, the
molecular weights and/or the melt indices of both the elastomer and
crystal polystyrene could be used to adjust the shrink curve of the
film to match the end use. For example, lower molecular weight
polymers have a lower softening point which moves the shrink curve
to the left. Also, the melt index of the elastomer and the crystal
polystyrene should be matched as close as possible in some
embodiments, and preferably, in other embodiments, no more than a
difference of 6 g flow/10 min at 200.degree. C. (ASTM D-1238G) is
desirable.
[0027] In a preferred embodiment, films are produced with a blend
of 70% crystal/high impact polystyrene and 30% elastomers. More
preferably, in some embodiments, the 70% crystal/high impact
polystyrene is predominantly crystal polystyrene, for example 68%
crystal polystyrene and 2% high impact polystyrene.
[0028] Processing
[0029] After the polymer composition of the film is selected, the
polymer is then processed to generate a film with desirable shrink
properties. Generally, the polymers are procured in pellets or
grains. In cases where multiple polymers are to be included, the
polymers pellets are first dry blended. That is, the pellets are
mixed together. The processing there from essentially comprises
five steps: drying, extrusion, temperature conditioning, orienting,
and annealing. Details of each processing step will now be
described.
[0030] The blended polymer pellets are first dried by heating in a
dryer to remove surface moisture. In some embodiments, a hot air
dryer is used; however, a variety of air dryers are known in the
art and many of them may be suitable for drying. The present
invention need not be limited to air dryers only, but may include
other types of dryers, including baking ovens. The temperature and
duration of drying may be dependent on the total amount and
condition of the polymer(s) (i.e., the amount of starting surface
moisture), and may need to be adjusted on a batch-by-batch basis.
Preferably, the polymers experience little to no melting in this
step. By way of example, typical drying conditions require that
temperatures range from about 27.degree. C. to about 94.degree. C.,
for variable periods of time. In some embodiments, polymers are
heated to 60.degree. C. for 3 hours before further processing. The
drying is thought to increase the likelihood of high level clarity
where clear shrink films are desired.
[0031] Extrusion, the second processing step, is whereby the
pellets are melted into a low viscosity molten mass, thus combining
the heretofore individual polymer beads or grains into one molten
mass. The viscosity of the melt will depend on the temperature.
Temperatures can range from about the temperature at which the
polymers will remain melted to about the temperature where
degradation of the polymers begins to occur. By way of example,
extrusion melt temperatures may be maintained between about
160.degree. C. to about 288.degree. C. for certain polymer blends,
but may ultimately depend on the different polymers that have been
blended and their respective melting points. In some embodiments,
200.degree. C., is preferred.
[0032] By way of example, the viscosity of 100% SBS polymer
(comprising 75% crystal polystyrene and 25% butadiene rubber), at
240.degree. C. and an apparent sheer rate of about 5.5
seconds.sup.-1 in a capillary rheometer, may range from about 6,000
poise (P, dyne/cm.sup.2) to about 11,000 P, preferably about 8,000
P to about 10,000 P, and more preferably, about 9,000 P. At a shear
rate of about 55 seconds.sup.-1 the same polymer at 240.degree. C.
may have an apparent viscosity that ranges from about 3,000 P to
about 6,000 P, preferably about 4,000 P to about 5,000 P, and more
preferably, about 4,500 P.
[0033] The third step, temperature conditioning, is done to
increase the viscosity of the molten polymers, which makes the melt
manageable for further processing. It is thought that by increasing
the viscosity, a smoother film surface than without this step is
generated. A smoother surface aids in the printing process that is
performed in many end applications, such as, for example,
labels.
[0034] The cooling step may be accomplished by a variety of methods
known in the art. However, it has now been found and that the use
of a polymer cooler at this step in processing may enable more
precise temperature control. It is believed that temperature
control over the orienting process which follows the controlled
cooling step allows for a controlled shrink memory to be stored in
the film.
[0035] A variety of coolers are known in the art and may be used by
one of ordinary skill in the art based on the teaching provided
herein. However, A Koch Engineering SIR polymer cooling unit,
available from Sulzer Chemtech, USA of Tulsa, Okla., adapted for
polystyrene use may be preferred in some applications.
[0036] The polymer cooler operating temperature range is preferably
between about 160.degree. C. to about 190.degree. C. Higher
temperatures may be used, but such higher temperatures may also
lead to less shrinkage of the film. The temperature and duration of
cooling can again depend on both the amount of polymer being cooled
and the film properties that may be desired. For example,
generally, a reduction in temperature is correlated with an
increase in shrinkage.
[0037] In one example, the viscosity of 100% SBS polymer
(comprising 75% Crystal polystyrene and 25% butadiene rubber), at
180.degree. C. and an apparent sheer rate of about 5.5
seconds.sup.-1 in a capillary remoter, may range from about 60,000
P to about 80,000 P, preferably about 65,000 P to about 75,000 P,
and more preferably, about 71,000 P. At a shear rate of about 55
seconds.sup.-1 the same polymer at 180.degree. C. may have an
apparent viscosity that ranges from about 16,000 P to about 19,500
P, preferably about 16,500 P to about 18,000 P, and more
preferably, about 17,500 P. It will be apparent from the data
presented herein that the polymer cooling step can increase the
viscosity from about 2 to about 10 times that of the polymer coming
out of the extruder. In other embodiments, the viscosity may be
increased about 5 to about 9 times.
[0038] The fourth step in preparation of films of the present
invention is orienting, also known as stretching. Orienting can be
accomplished by many methods and associated equipment known to one
of ordinary skill in the art, including, for example, machine
direction orientation and blown film orientation. All methods are
preferably designed to first control the temperature of the
polymer, followed by a controlled stretching operation.
[0039] In a preferred embodiment of the present invention, the
polymer melt is already pre-cooled, preferably in a polymer cooler,
and then submitted to a blown film orientation process. Pre-cooling
the polymer in a polymer cooler before blown film orienting is
believed to be unique. The process of the present invention has one
significant advantage in that a very controlled temperature--from
the post extrusion temperature conditioning--can be achieved prior
to the formation of a bubble. A blown film extrusion process blows
molten plastic polymer through a die of circular cross-section into
a bubble using an air jet. Once the plastic has been blown out,
rollers flatten it into a sheet of double-thickness film. It can
then be cut to form two sheets of film. The sheets of film can then
be cut to desired length.
[0040] In the preferred embodiment then, by virtue of pre-cooling
the melted polymer, only a final fine tuning of orienting
temperature is performed, where desired, during the orientation
process. In other words, the greater share of temperature
conditioning takes place prior to orienting and not during
orienting. Where a fine tuning of temperature is desired, it can be
relatively easily accomplished by a temperature controlled air
ring, which blows chilled air at the base of the bubble.
[0041] The orienting process imparts the shrink memory into the
film where it is stored by the different polymers that are used.
Die parameters may range from 1:0.75 BUR (Blown Up Ratio) to about
1:3 BUR, and preferably, about 1:1.4 BUR in the cross web
direction. In the length (or machine) direction, die parameters may
range from about 1:1 draw down ratio to about 1:300 draw down
ratio, and preferably, about 1:130 draw down ratio. Orienting
temperatures of the present invention range from about 65.degree.
C. to about 160.degree. C., and more preferably, about 120.degree.
C.
[0042] Annealing, also called relaxation, is the final step in the
preparation of films of the instant invention. Annealing is
generally accomplished post orienting, and performed at
temperatures between about 27.degree. C. to about 176.degree. C. in
some embodiments, and more preferably at 90.degree. C. This process
is accomplished by rotating heated cylinders that contact the film
just prior to the winding process where the finished roll of
plastic film is generated.
[0043] Film properties using the aforementioned protocol can be
manipulated as desired with nominal trial and error by one of
ordinary skill in the art. Such variations are expected and are
incorporated into the scope of the invention. Films of the instant
invention, can generally have characteristics that fall into the
following ranges:
[0044] Film Shrinkage at about 120.degree. C. for about 5 minutes
in air:
[0045] Longitudinal direction: about 10% to about 90%, with an
average of about 50%.
[0046] Cross direction: about +30% (shrinkage) to about -30%
(growth), with an average of about -5%.
[0047] FIGS. 1, 2, and 3 show the percent shrinkage as a function
of temperature of 120 gauge (0.0012 in.), 160 gauge (0.0016 in.),
and 200 gauge (0.002 in.) films, respectively. The films were
prepared from a blend of about 68% crystal polystyrene, about 30%
elastomers and about 2% high impact polystyrene. Using the
preferred process described above, the blend was dried at
60.degree. C. for about 3 hours, extruded at about 200.degree. C.,
and cooled in a polymer cooler to below 190.degree. C. The cooled
polymer was subsequently blow film oriented at 120.degree. C. and
finally annealed at 90.degree. C. Die ratios were 1:1.4 in the
cross web direction and 1:130 in the machine direction.
[0048] The respective films were placed in a hot air dryer at the
temperature shown for about five minutes and the shrinkage in the
longitudinal direction and the cross direction as a percentage of
the original dimensions is plotted. As is evident from the results,
the films described exhibit positive shrinkage in the longitudinal
direction and negative shrinkage (i.e., growth or expansion) in the
cross direction at all the temperatures tested.
[0049] This growth in the cross direction can prevent the label
from curling back on the edges during the shrinking process.
Accordingly, in one embodiment, films of the present invention may
have application in roll to roll (i.e., wrap around) labeling of
various shaped cylinders such as, for example, batteries, cans,
bottles, disposable lighters, pens and other decorative items.
However, the scope of applications should not be limited to the
aforementioned consumer products or uses.
[0050] Films of the present invention have innumerable other
applications. For example, these films can also be used in
printed/unprinted application for holding together twin packs,
attachments, neck bands, and perforated neck bands for decoration
or tamper evident use, to name a few options.
[0051] The many features and advantages of the invention are
apparent from the detailed specification, and thus, it is intended
by the appended claims to cover all such features and advantages of
the invention, which fall within the spirit and scope of the
invention. Further, since numerous modifications and variations
will readily occur to those skilled in the art, it is not desired
to limit the invention to the exact construction and operation
illustrated and described, and accordingly, all suitable
modifications and equivalents may be resorted to, fall within the
scope of the invention.
* * * * *