U.S. patent application number 13/972025 was filed with the patent office on 2015-07-09 for pressure sensitive shrink label.
This patent application is currently assigned to Avery Dennison Corporation. The applicant listed for this patent is Avery Dennison Corporation. Invention is credited to William L. CONE, James P. LORENCE, Richard D. PASTOR, Craig W. POTTER, Mitchell J. RACKOVAN.
Application Number | 20150191632 13/972025 |
Document ID | / |
Family ID | 39645694 |
Filed Date | 2015-07-09 |
United States Patent
Application |
20150191632 |
Kind Code |
A1 |
LORENCE; James P. ; et
al. |
July 9, 2015 |
Pressure Sensitive Shrink Label
Abstract
A label for application to a surface having at least one
compound curve is provided. The label comprises a heat shrinkable
film having an inner surface and outer surface and a layer of
pressure sensitive adhesive on the inner surface of the heat
shrinkable film.
Inventors: |
LORENCE; James P.;
(Painesville, OH) ; RACKOVAN; Mitchell J.;
(Madison, OH) ; POTTER; Craig W.; (Mentor, OH)
; PASTOR; Richard D.; (Lyndhurst, OH) ; CONE;
William L.; (Weeki Wachee, FL) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Avery Dennison Corporation |
Pasadena |
CA |
US |
|
|
Assignee: |
Avery Dennison Corporation
Pasadena
CA
|
Family ID: |
39645694 |
Appl. No.: |
13/972025 |
Filed: |
August 21, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12532845 |
Sep 24, 2009 |
8535464 |
|
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PCT/US2008/059397 |
Apr 4, 2008 |
|
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13972025 |
|
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60910282 |
Apr 5, 2007 |
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60938019 |
May 15, 2007 |
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Current U.S.
Class: |
428/41.8 ;
428/195.1; 428/201; 428/343; 428/347; 428/354 |
Current CPC
Class: |
Y10T 428/24868 20150115;
C09J 7/385 20180101; C09J 2467/006 20130101; G09F 2003/0257
20130101; Y10T 428/1476 20150115; C09J 2203/334 20130101; C09J
2427/006 20130101; C09J 2423/006 20130101; B65C 9/24 20130101; G09F
2003/0208 20130101; C09J 7/29 20180101; Y10T 428/2817 20150115;
Y10T 428/2848 20150115; C09J 2425/006 20130101; C09J 2301/162
20200801; B65C 9/36 20130101; B65D 25/205 20130101; G09F 2003/0241
20130101; B65C 9/26 20130101; C09J 2301/204 20200801; Y10T
428/24851 20150115; C09J 7/22 20180101; Y10T 428/24802 20150115;
C09J 2301/312 20200801; Y10T 156/10 20150115; Y10T 428/24628
20150115; Y10T 428/28 20150115; G09F 3/02 20130101; G09F 3/10
20130101; G09F 2003/0272 20130101; B65C 9/20 20130101 |
International
Class: |
C09J 7/02 20060101
C09J007/02; G09F 3/02 20060101 G09F003/02 |
Claims
1. A pressure sensitive adhesive label for application on a surface
having at least one compound curve, the label comprising: a heat
shrinkable film having an inner surface and outer surface, and a
machine direction and a trans direction, the film having an
ultimate shrinkage S in at least one direction of at least 10% at
90.degree. C. as measured by ASTM Method D1204, wherein the
shrinkage in the other direction is within the range of S.+-.20%;
and a continuous adhesive layer of pressure sensitive adhesive
having an interior surface and an exterior surface, wherein the
interior surface of the adhesive layer is adhered to the inner
surface of the heat shrinkable film and the exterior surface is
capable of adhering to the surface having at least one compound
curve.
2. The label of claim 1 wherein the label is sized such that it
does not adhere to itself when placed on a surface having a
compound curve.
3. The label of claim 1 wherein the heat shrinkable film comprises
a film selected from polyester, polyolefin, polyvinyl chloride,
polystyrene, poly lactic acid, copolymers thereof and blends
thereof.
4. The label of claim 1 wherein the heat shrinkable film comprises
a multilayer film having a core layer and at least one skin
layer.
5. The label of claim 1 wherein the stiffness of the film is at
least 5 mN in the machine direction.
6. The label of claim 1 further comprising a print layer between
the heat shrinkable film and the adhesive layer, wherein the heat
shrinkable film is transparent.
7. The label of claim 1 further comprising a print layer on the
outer surface of the heat shrinkable film.
8. The label of claim 8 further comprising a protective layer
overlying the print layer.
9. The label of claim 1 wherein the adhesive layer comprises an
emulsion adhesive, hot melt adhesive or solvent based adhesive.
10. The label of claim 1 wherein the heat shrinkable film comprises
a multilayer coextruded film.
11. The label of claim 1 further comprising a release liner adhered
to the pressure sensitive adhesive.
12. The label of claim 1 wherein the continuous pressure sensitive
adhesive layer is a continuous pattern and the pattern
substantially covers the inner surface of the film.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] The present application is a division of U.S. patent
application Ser. No. 12/532,845 filed Sep. 24, 2009, which is a 371
of International Application No. PCT/US2008/059397, which was
published in English on Oct. 16, 2008, which claims priority from
U.S. Provisional Application No. 60/910,282 filed Apr. 5, 2007, and
U.S. Provisional Application No. 60/938,019 filed May 15, 2007, all
of which are incorporated herein by reference in their
entireties.
FIELD
[0002] This invention relates to pressure sensitive shrink labels.
More specifically, the invention relates to pressure sensitive
labels that have superior conformability to containers having
complex shapes and methods for applying such labels.
BACKGROUND
[0003] It is common practice to apply labels to containers or
bottles to provide information such as the supplier of the
container or the contents of the container. Such containers and
bottles are available in a wide variety of shapes and sizes for
holding many different types of materials such as detergents,
chemicals, personal care products, motor oil, beverages, etc.
[0004] Polymeric film materials and film facestocks have been
described for use as labels in various fields. Polymeric labels are
increasingly desired for many applications, particularly clear
polymeric labels since they provide a no-label look to decorated
glass and plastic containers. Paper labels block the visibility of
the container and/or the contents in the container. Clear polymeric
labels enhance the visual aesthetics of the container, and
therefore the product, and are growing much faster than paper
labels in the package decoration market as consumer product
companies are continuously trying to upgrade the appearance of
their products. Polymeric film labels also have superior mechanical
properties, such as tensile strength and abrasion resistance.
[0005] Traditional pressure sensitive adhesive (PSA) labels often
have difficulty adhering smoothly to containers having curved
surfaces and/or complex shapes without wrinkling, darting or
lifting on the curved surfaces. The label size of typical PSA
labels is limited to no larger than 1/4 inch away from the edge
(beginning) of curvature of a container or article. Shrink sleeve
labels have typically been used on these types of compound
containers. Labeling operations are carried out using processes and
methods that require the formation of a tube or sleeve of the heat
shrink film that is placed over the container and heated in order
to shrink the film to conform to the size and shape of the
container. Alternatively, the containers are completely wrapped
with a shrink label using a process wherein the shrink film is
applied to the container directly from a continuous roll of film
material and then heat is applied to conform the wrapped label to
the container. However, label defects can occur during labeling
operations of simple or compound shaped bottles during application
or in post application processes. These misapplied labels result in
high scrap or extra processing steps that can be costly.
[0006] The present invention provides a pressure sensitive adhesive
label that can be applied to containers and articles on complex
shapes and compound curves with less material required and less
cost than for shrink sleeve or shrink wrap labels. In addition, the
labels of the present invention enable the user to expand the
billboard or graphics region of traditional pressure sensitive
labels on containers and articles having complex shapes and/or
compound curves.
SUMMARY
[0007] A label for application on a curved or nonplanar surface
comprising a heat shrink film and a pressure sensitive adhesive is
provided. In one embodiment, there is provided a pressure sensitive
adhesive label for application on a surface having at least one
compound curve, the label comprising: a heat shrinkable film having
an inner surface and outer surface, and a machine direction and a
trans direction, the film having an ultimate shrinkage S in at
least one direction of at least 10% at 90.degree. C., wherein the
shrinkage in the other direction is S.+-.20%; and a layer of
pressure sensitive adhesive on the inner surface of the heat
shrinkable film. The shrink film has moderate and balanced shrink
in both the machine direction and the trans direction. In one
embodiment, the film has an ultimate shrinkage S in at least one
direction of at least 10% at 90.degree. C., and the shrinkage in
the other direction is S.+-.10%. The label may further include a
release liner removal adhered to the adhesive layer.
[0008] There is also provided an article bearing a label
comprising: an article having a surface comprising at least one
compound curve; and a pressure sensitive label comprising a heat
shrinkable film having an inner surface and outer surface, and a
layer of pressure sensitive adhesive on the inner surface of the
heat shrinkable film, wherein the label is applied to at least one
compound curve.
[0009] A method of applying a label to an article wherein the
article has a surface having at least one compound curve is
provided. The method comprises: (a) providing an article having a
surface comprising at least one compound curve; (b) providing a
label comprising (i) a heat shrinkable film having an inner surface
and outer surface and (ii) a layer of pressure sensitive adhesive
on the inner surface of the heat shrinkable film, wherein the label
has a central portion and a peripheral portion; (c) contacting the
adhesive layer of the central portion of the label with the
article; (d) applying pressure to the label in an outward direction
from the central portion to the peripheral portion, wherein at
least a portion of the label is applied to at least one compound
curve of the article; and (e) applying heat to at least a portion
of the label to shrink at least that portion of the label and
adhere the label to the article. After or during the application of
heat, the label may be further compressed or wiped down to fully
adhere the label to the article and eliminate any remaining defects
in the label.
BRIEF DESCRIPTION OF DRAWINGS
[0010] FIG. 1 illustrates a front view of a container to which the
label of the present invention has been applied as compared to
prior art pressure sensitive labels.
[0011] FIG. 2A to 2D illustrates the labeled container before and
after the application of heat to the label.
[0012] FIG. 3A to 3D illustrate embodiments of containers having
complex shapes and compound curves to which the label of the
present invention is applied.
[0013] FIGS. 4A and 4B illustrate front views of embodiments of
containers having irregular surfaces.
[0014] FIG. 5 is a three dimensional view of a portion of a labeled
article having a compound curve.
[0015] FIGS. 6A to 6D schematically illustrates the process of
applying the label to an article having a compound curve.
[0016] FIGS. 7A to 7B schematically illustrates an embodiment of
the process of applying a label to an article wherein a walking
beam is used.
DETAILED DESCRIPTION
[0017] Pressure sensitive adhesive labels are provided that can
improve the appearance of labeled containers and articles by
conforming to the contours of the container or article and by
providing an enlarged billboard appearance. End users and product
designers must currently alter their designs to accommodate the
limitations of traditional product decorating technologies. The
labels of the present invention provide the designers with more
freedom in product designs to create more shelf appeal and to carry
more information.
[0018] Containers and articles with compound curves typically have
to be fully wrapped with shrink film in order to label or decorate
the article. The labels of the present invention are capable of
expanding the label over complex curves without having to fully
wrap the article. This partial label coverage impacts the product
cost as well as the product appearance. Typical pressure sensitive
labels cannot be applied to containers and articles without
undesirable darting and wrinkling of the label. "Darting" is
defined as the accumulation of excess label material that raises up
away from the article to which the label is applied.
[0019] The labels of the present invention provide significant
processing advantages over traditional shrink labels. For example,
the pressure sensitive shrink labels of the present invention allow
for more traditional printing and secondary processes such as foils
and hot stamping. Where typical shrink labels must be subsurface
printed, the labels of the present invention can be surface
printed, which enhances the color quality, sharpness and texture of
the printed image. The label film may be printed by water
flexographic, UV flexographic, UV letterpress, UV screen, solvent
gravure and hot foil stamp.
[0020] The pressure sensitive labels comprise (a) a heat shrinkable
polymeric film having an inner surface and an outer surface and a
machine direction and a trans direction; and (b) a layer of
pressure sensitive adhesive on the inner surface of the heat
shrinkable film. The shrinkage of the heat shrinkable polymeric
film is balanced in the machine direction and the trans direction.
In at least one direction, the ultimate shrinkage (S) is at least
10% at 90.degree. C. and in the other direction, the shrinkage is
S.+-.20%. As an illustration of balanced shrinkage, if the
shrinkage in the machine direction is 40% at 105.degree. C., then
the shrinkage in the trans direction is 40%.+-.20%, or within the
range of 20% to 60% at 105.degree. C. In one embodiment, the
ultimate shrinkage (S) is at least 10% at 90.degree. C. and in the
other direction, the shrinkage is S.+-.10%. As used herein, the
term "ultimate shrinkage" means the maximum shrinkage the film is
capable of achieving at a particular shrink temperature, as
measured by ASTM Method D 1204.
[0021] The labels are not provided as a shrink sleeve or tube that
encapsulates the entire article or as a shrink wrap label that
wraps around the article and forms a seam wherein the ends of the
label meet. The present labels may be provided in a variety of
shapes to suit the article or container to which they are applied,
giving the container designer greater latitude in container
configuration and label design than with traditional pressure
sensitive labels or with shrink wrap or shrink sleeve labels. The
labels may be cut into the desired shape by any known method,
including, for example, die cutting and laser cutting. In one
embodiment, the label is die cut to a specific configuration that
compensates for the shrinkage of the label and the shape of the
article to which it is applied.
[0022] Because the label is conformable, the billboard or graphics
area of the labeled container can be extended further onto the
container edges and onto compound curved areas of the container.
The label may be 10% to 30% larger than a standard PSA label. As
used herein, the term "compound curve" means a surface having no
direction for which there is no curvature. For example, the surface
of a sphere or the surface of an ellipsoid has curvature in every
direction, and therefore has compound curves. A cylinder, on the
other hand, has a surface for which there is at least one direction
for which there is no curvature. Thus, a simple cylinder does not
have compound curves.
[0023] FIG. 1 illustrates the expanded billboard area of the
pressure sensitive shrink label of the present invention. Bottle 10
has pressure sensitive shrink label 12 adhered thereto. The dashed
line 14 indicates the outer boundary of standard pressure sensitive
labels. A standard (i.e., non-shrink) pressure sensitive label
cannot extend onto the areas of the bottle having the compound
curves 16 (the area between the inner dashed line and the outer
solid line). When label 12 is initially applied to the bottle 10,
darts and pleats may form near the perimeter of the label in the
areas of the bottle having compound curves 16.
[0024] Once the pressure sensitive label is applied to the
container, heat is applied as needed to eliminate any label
application defects such as darts, edge lift and wrinkles. In one
embodiment, pressure and/or wipe down may be used in addition to
the application of heat to eliminate any defects.
[0025] Referring to FIGS. 2A-2D, the present label and method for
applying the label are illustrated. In FIGS. 2A and 2B, a label 12
that includes a shrink film having a continuous layer of pressure
sensitive adhesive applied thereto is applied to a container 10
having compound curves around the circumference of the container,
and then wiped down. No heat is applied to the label. The label 12
extends onto the compound curves 16 where darts 18 are formed near
the perimeter 20 of the label. FIGS. 2C and 2D show the labeled
container of FIGS. 2A-2B after heat is applied to the label. The
darts 18 have been eliminated and the label 12 conforms to the
compound curves of the container 10 near the label perimeter 20
without any defects.
[0026] The article or container to which the label is applied can
be provided in a variety of forms or shapes. Non-limiting examples
of suitable articles include containers with and without closures,
trays, lids, toys, appliances, etc. The article or container may be
made of any conventional polymer, glass, or metal such as aluminum.
Examples of suitable polymeric materials include high density
polyethylene (HDPE), low density polyethylene (LDPE), polyethylene
terephthalate (PET), polypropylene (PP), polyvinyl chloride,
polycarbonate, nylon, fluorinated ethylene propylene, polystyrene,
etc. The article or container can be made by a number of various
processes known in the art, such as blow molding, injection
molding, thermoforming, rotational molding and the like.
[0027] Useful containers include, for example, a bottle having a
closure on the top of the bottle, an upside down bottle having a
closure on the bottom of the bottle, a bottle with a pump dispenser
or a foaming dispenser, a tube with a closure and a tottle with a
closure.
[0028] The container or article may have a transparent appearance.
In one embodiment, the container or article has a translucent
appearance. The translucent appearance can be achieved by, for
example, treatments of the transparent container or article, the
addition of ingredients such as dyes and pearlescent agents to base
polymers, the use of polypropylene and/or polyethylene that are
mixed with clarifying agents. The treatments include, for example,
spray coating, sandblasting, and mold surface treatment.
[0029] The container or article may include aesthetic features,
including, for example, textures, embossing, lenticular lens,
colors, holograms, frosted or matte color, etc. The surface of the
container or article may be treated prior to application of the
label. For example, the surface of the container or article may be
flame treated or a primer coating may be applied.
[0030] FIGS. 3A, 3B and 3C each illustrate a container having a
complex shape and compound curves. FIG. 3A is a front view of a
container 30a having a symmetrical, spherical shape wherein the
container has a tapered concave area 32 at the top and a wider
convex area 33 toward the bottom. Typically, a shrink sleeve would
be used to provide a functional label for this container. With the
present invention, a pressure sensitive shrink label 31 can be
smoothly applied to container 30a without the appearance of label
defects. FIG. 3B is a front view of a container 30b having an
asymmetrical shape wherein one side of the container has both a
concave area 34 and a convex area 35 and the opposing side curves
in a substantially similar manner along the length of the
container. The conventional method of labeling container 30b would
be to apply a shrink sleeve label to conform to the complex shape
of the container. A pressure sensitive shrink label 31 can be
applied to the container 30b to provide sufficient billboard area
with much less label material. FIG. 3C is a front view of a
container 30c that is an upside down bottle having a closure 36 at
the bottom and label 31 applied to the front surface. FIG. 3D is a
side view of container 30c. The areas 37 within the dashed lines
indicate the outer boundaries of standard pressure sensitive labels
that can be applied to the container. The complex shape of this
container requires two separate standard pressure sensitive labels
to decorate the container, as the application of one continuous
standard pressure sensitive label would result in the formation of
darts and pleat defects. Pressure sensitive shrink label 31 can
cover a much larger area, which provides more design options for
the product designer.
[0031] FIGS. 4A and 4B each illustrate a container having an
irregular surface. FIG. 4A is a front view of a container 40a
having raised ridges 42 along one side of the container. The
opposing side of the container has a smooth surface. FIG. 4B is a
front view of a container 40b having circumferentially recessed
rings 43 along the length of the container. It should be noted that
cylindrically shaped articles having areas of compound curves such
as containers 40a and 40b are not excluded from the articles
claimed herein.
[0032] FIG. 5 is a schematic three dimensional view of a portion of
a container to which the label has been applied. The container 50
has surface comprising a compound curve. Label 52 is applied to the
container and covers a portion of the compound curved area. Line 54
indicates the outer boundary to which typical pressure sensitive
labels can be applied with out the formation of defects in the
label. Area 56 indicates the expanded billboard area that is
obtainable with the present labels without the formation of defects
such wrinkles, edge lift or darts.
Shrink Film
[0033] The polymeric films useful in the label constructions of the
present invention possess balanced shrink properties. The balanced
shrink properties allow the film to tighten darts and wrinkles
initially formed in the label when the label is applied over curved
surfaces and allow the darts and wrinkles to be wiped down with
minimal graphics distortion of the label. Films having unbalanced
shrink, that is, films having a high degree of shrink in one
direction and low to moderate shrink in the other direction are not
particularly useful because while darts may be removed in one
direction, in the other direction the formation of darts is
exacerbated. Useful films having balanced shrink allow for a wider
variety of label shapes to be applied to a wider variety of
container shapes.
[0034] In one embodiment, the polymeric film has an ultimate
shrinkage (S) as measured by ASTM procedure D1204 in at least one
direction of at least 10% at 90.degree. C. and in the other
direction, the shrinkage is S.+-.20%. In another embodiment, the
film has an ultimate shrinkage (S) in at least one direction of
about 10% to about 50% at 70.degree. C. and in the other direction,
the shrinkage is S.+-.20%. In one embodiment, the ultimate
shrinkage (S) is at least 10% at 90.degree. C. and in the other
direction, the shrinkage is S.+-.10%. The shrink initiation
temperature of the film, in one embodiment, is in the range of
about 60.degree. C. to about 80.degree. C.
[0035] The shrink film must be thermally shrinkable and yet have
sufficient stiffness to be dispensed using conventional labeling
equipment and processes, including printing, cutting and label
transfer. The stiffness of the film required depends on the size of
the label, the speed of application and the labeling equipment
being used. In one embodiment, the shrink film has a stiffness in
the machine direction (MD) of at least 5 mN, as measured by the
L&W Bending Resistance test. In one embodiment, the shrink film
has a stiffness of at least 10 mN, or at least 20 mN.
[0036] In one embodiment, the shrink film has a 2% secant modulus
as measured by ASTM D882 in the machine direction (MD) of about
20,000 to about 400,000 psi, and in the trans (or cross) direction
(TD) of about 20,000 to about 400,000 psi. In another embodiment,
the 2% secant modulus of the film is about 30,000 to about 300,000
in the machine direction and about 30,000 to about 300,000 in the
trans direction. The film may have a lower modulus in the trans
direction than in the machine direction so that the label is easily
dispensed (MD) while maintaining sufficiently low modulus in the TD
for conformability and/or squeezability.
[0037] The polymeric film may be made by conventional processes.
For example, the film may be produced using a double bubble
process, tenter process or may comprise a blown film.
[0038] he shrink film useful in the label may be a single layer
construction or a multilayer construction. The layer or layers of
the shrink film may be formed from a polymer chosen from polyester,
polyolefin, polyvinyl chloride, polystyrene, polylactic acid,
copolymers and blends thereof.
[0039] Polyolefins comprise homopolymers or copolymers of olefins
that are aliphatic hydrocarbons having one or more carbon to carbon
double bonds. Olefins include alkenes that comprise 1-alkenes, also
known as alpha-olefins, such as 1-butene and internal alkenes
having the carbon to carbon double bond on nonterminal carbon atoms
of the carbon chain, such as 2-butene, cyclic olefins having one or
more carbon to carbon double bonds, such as cyclohexene and
norbornadiene, and cyclic polyenes which are noncyclic aliphatic
hydrocarbons having two or more carbon to carbon double bonds, such
as 1,4-butadiene and isoprene. Polyolefins comprise alkene
homopolymers from a single alkene monomer, such as a polypropylene
homopolymer, alkene copolymers from at least one alkene monomer and
one or more additional olefin monomers where the first listed
alkene is the major constituent of the copolymer, such as a
propylene-ethylene copolymer and a propylene-ethylene-butadiene
copolymer, cyclic olefin homopolymers from a single cyclic olefin
monomer, and cyclic olefin copolymers from at least one cyclic
olefin monomer and one or more additional olefin monomers wherein
the first listed cyclic olefin is the major constituent of the
copolymer, and mixtures of any of the foregoing olefin
polymers.
[0040] In one embodiment, the shrink film is a multilayer film
comprising a core layer and at least one skin layer. The skin layer
may be a printable skin layer. In one embodiment, the multilayer
shrink film comprises a core and two skin layers, wherein in at
least one skin layer is printable. The multilayer shrink film may
be a coextruded film.
[0041] The film can range in thickness from 0.5-20, or 0.5-12, or
0.5-8, or 1-3 mils. The difference in the layers of the film can
include a difference in thermoplastic polymer components, in
additive components, in orientation, in thickness, or a combination
thereof. The thickness of the core layer can be 50-95%, or 60-95%
or 70-90% of the thickness of the film. The thickness of a skin
layer or of a combination of two skin layers can be 5-50%, or 5-40%
or 10-30% of the thickness of the film.
[0042] The film can be further treated on one surface or both the
upper and lower surfaces to enhance performance in terms of
printability or adhesion to an adhesive. The treatment can comprise
applying a surface coating such as, for example, a lacquer,
applying a high energy discharge to include a corona discharge to a
surface, applying a flame treatment to a surface, or a combination
of any of the foregoing treatments. In an embodiment of the
invention, the film is treated on both surfaces, and in another
embodiment the film is treated on one surface with a corona
discharge and is flame treated on the other surface.
[0043] The layers of the shrink film may contain pigments, fillers,
stabilizers, light protective agents or other suitable modifying
agents if desired. The film may also contain anti-block, slip
additives and anti-static agents. Useful anti-block agents include
inorganic particles, such as clays, talc, calcium carbonate and
glass. Slip additives useful in the present invention include
polysiloxanes, waxes, fatty amides, fatty acids, metal soaps and
particulate such as silica, synthetic amorphous silica and
polytetrafluoroethylene powder. Anti-static agents useful in the
present invention include alkali metal sulfonates,
polyether-modified polydiorganosiloxanes, polyalkylphenylsiloxanes
and tertiary amines.
[0044] In one embodiment, the shrink film is microperforated to
allow trapped air to be released from the interface between the
label and the article to which it is adhered. In another
embodiment, the shrink film is permeable to allow fluid to escape
from the adhesive or from the surface of the article to escape. In
one embodiment, vent holes or slits are provided in the shrink
film.
Adhesives
[0045] A description of useful pressure sensitive adhesives may be
found in Encyclopedia of Polymer Science and Engineering, Vol. 13,
Wiley-Interscience Publishers (New York, 1988). Additional
description of useful PSAs may be found in Polymer Science and
Technology, Vol. 1, Interscience Publishers (New York, 1964).
Conventional PSAs, including acrylic-based PSAs, rubber-based PSAs
and silicone-based PSAs are useful. The PSA may be a solvent based
or may be a water based adhesive. Hot melt adhesives may also be
used. In one embodiment, the PSA comprises an acrylic emulsion
adhesive.
[0046] The adhesive and the side of the film to which the adhesive
is applied have sufficient compatibility to enable good adhesive
anchorage. In one embodiment, the adhesive is chosen so that the
labels may be cleanly removed from PET containers up to 24 hours
after application. The adhesive is also chosen so that the adhesive
components do not migrate into the film.
[0047] In one embodiment, the adhesive may be formed from an
acrylic based polymer. It is contemplated that any acrylic based
polymer capable of forming an adhesive layer with sufficient tack
to adhere to a substrate may function in the present invention. In
certain embodiments, the acrylic polymers for the
pressure-sensitive adhesive layers include those formed from
polymerization of at least one alkyl acrylate monomer containing
from about 4 to about 12 carbon atoms in the alkyl group, and
present in an amount from about 35-95% by weight of the polymer or
copolymer, as disclosed in U.S. Pat. No. 5,264,532. Optionally, the
acrylic based pressure-sensitive adhesive might be formed from a
single polymeric species.
[0048] The glass transition temperature of a PSA layer comprising
acrylic polymers can be varied by adjusting the amount of polar, or
"hard monomers", in the copolymer, as taught by U.S. Pat. No.
5,264,532, incorporated herein by reference. The greater the
percentage by weight of hard monomers is an acrylic copolymer, the
higher the glass transition temperature. Hard monomers contemplated
useful for the present invention include vinyl esters, carboxylic
acids, and methacrylates, in concentrations by weight ranging from
about zero to about thirty-five percent by weight of the
polymer.
[0049] The PSA can be acrylic based such as those taught in U.S.
Pat. No. 5,164,444 (acrylic emulsion), U.S. Pat. No. 5,623,011
(tackified acrylic emulsion) and U.S. Pat. No. 6,306,982. The
adhesive can also be rubber-based such as those taught in U.S. Pat.
No. 5,705,551 (rubber hot melt). It can also be radiation curable
mixture of monomers with initiators and other ingredients such as
those taught in U.S. Pat. No. 5,232,958 (UV cured acrylic) and U.S.
Pat. No. 5,232,958 (EB cured). The disclosures of these patents as
they relate to acrylic adhesives are hereby incorporated by
reference.
[0050] Commercially available PSAs are useful in the invention.
Examples of these adhesives include the hot melt PSAs available
from H.B. Fuller Company, St. Paul, Minn. as HM-1597, HL-2207-X,
HL-2115-X, HL-2193-X. Other useful commercially available PSAs
include those available from Century Adhesives Corporation,
Columbus, Ohio. Another useful acrylic PSA comprises a blend of
emulsion polymer particles with dispersion tackifier particles as
generally described in Example 2 of U.S. Pat. No. 6,306,982. The
polymer is made by emulsion polymerization of 2-ethylhexyl
acrylate, vinyl acetate, dioctyl maleate, and acrylic and
methacrylic comonomers as described in U.S. Pat. No. 5,164,444
resulting in the latex particle size of about 0.2 microns in weight
average diameters and a gel content of about 60%.
[0051] A commercial example of a hot melt adhesive is H2187-01,
sold by Ato Findley, Inc., of Wauwatusa, Wis. In addition, rubber
based block copolymer PSAs described in U.S. Pat. No. 3,239,478
also can be utilized in the adhesive constructions of the present
invention, and this patent is hereby incorporated by a reference
for its disclosure of such hot melt adhesives that are described
more fully below.
[0052] In another embodiment, the pressure-sensitive adhesive
comprises rubber based elastomer materials containing useful rubber
based elastomer materials include linear, branched, grafted, or
radial block copolymers represented by the diblock structure A-B,
the triblock A-B-A, the radial or coupled structures (A-B).sub.n,
and combinations of these where A represents a hard thermoplastic
phase or block which is non-rubbery or glassy or crystalline at
room temperature but fluid at higher temperatures, and B represents
a soft block which is rubbery or elastomeric at service or room
temperature. These thermoplastic elastomers may comprise from about
75% to about 95% by weight of rubbery segments and from about 5% to
about 25% by weight of non-rubbery segments.
[0053] The non-rubbery segments or hard blocks comprise polymers of
mono- and polycyclic aromatic hydrocarbons, and more particularly
vinyl-substituted aromatic hydrocarbons that may be monocyclic or
bicyclic in nature. Rubbery materials such as polyisoprene,
polybutadiene, and styrene butadiene rubbers may be used to form
the rubbery block or segment. Particularly useful rubbery segments
include polydienes and saturated olefin rubbers of
ethylene/butylene or ethylene/propylene copolymers. The latter
rubbers may be obtained from the corresponding unsaturated
polyalkylene moieties such as polybutadiene and polyisoprene by
hydrogenation thereof.
[0054] The block copolymers of vinyl aromatic hydrocarbons and
conjugated dienes that may be utilized include any of those that
exhibit elastomeric properties. The block copolymers may be
diblock, triblock, multiblock, starblock, polyblock or graftblock
copolymers. Throughout this specification, the terms diblock,
triblock, multiblock, polyblock, and graft or grafted-block with
respect to the structural features of block copolymers are to be
given their normal meaning as defined in the literature such as in
the Encyclopedia of Polymer Science and Engineering, Vol. 2, (1985)
John Wiley & Sons, Inc., New York, pp. 325-326, and by J. E.
McGrath in Block Copolymers, Science Technology, Dale J. Meier,
Ed., Harwood Academic Publishers, 1979, at pages 1-5.
[0055] Such block copolymers may contain various ratios of
conjugated dienes to vinyl aromatic hydrocarbons including those
containing up to about 40% by weight of vinyl aromatic hydrocarbon.
Accordingly, multi-block copolymers may be utilized which are
linear or radial symmetric or asymmetric and which have structures
represented by the formulae A-B, A-B-A, A-B-A-B, B-A-B,
(AB).sub.0,1,2 . . . BA, etc., wherein A is a polymer block of a
vinyl aromatic hydrocarbon or a conjugated diene/vinyl aromatic
hydrocarbon tapered copolymer block, and B is a rubbery polymer
block of a conjugated diene.
[0056] The block copolymers may be prepared by any of the
well-known block polymerization or copolymerization procedures
including sequential addition of monomer, incremental addition of
monomer, or coupling techniques as illustrated in, for example,
U.S. Pat. Nos. 3,251,905; 3,390,207; 3,598,887; and 4,219,627. As
well known, tapered copolymer blocks can be incorporated in the
multi-block copolymers by copolymerizing a mixture of conjugated
diene and vinyl aromatic hydrocarbon monomers utilizing the
difference in their copolymerization reactivity rates. Various
patents describe the preparation of multi-block copolymers
containing tapered copolymer blocks including U.S. Pat. Nos.
3,251,905; 3,639,521; and 4,208,356, the disclosures of which are
hereby incorporated by reference.
[0057] Conjugated dienes that may be utilized to prepare the
polymers and copolymers are those containing from 4 to about 10
carbon atoms and more generally, from 4 to 6 carbon atoms. Examples
include from 1,3-butadiene, 2-methyl-1,3-butadiene(isoprene),
2,3-dimethyl-1,3-butadiene, chloroprene, 1,3-pentadiene,
1,3-hexadiene, etc. Mixtures of these conjugated dienes also may be
used.
[0058] Examples of vinyl aromatic hydrocarbons which may be
utilized to prepare the copolymers include styrene and the various
substituted styrenes such as o-methylstyrene, p-methylstyrene,
p-tert-butylstyrene, 1,3-dimethylstyrene, alpha-methylstyrene,
beta-methylstyrene, p-isopropylstyrene, 2,3-dimethylstyrene,
o-chlorostyrene, p-chlorostyrene, o-bromostyrene,
2-chloro-4-methylstyrene, etc.
[0059] Many of the above-described copolymers of conjugated dienes
and vinyl aromatic compounds are commercially available. The number
average molecular weight of the block copolymers, prior to
hydrogenation, is from about 20,000 to about 500,000, or from about
40,000 to about 300,000.
[0060] The average molecular weights of the individual blocks
within the copolymers may vary within certain limits. In most
instances, the vinyl aromatic block will have a number average
molecular weight in the order of about 2000 to about 125,000, or
between about 4000 and 60,000. The conjugated diene blocks either
before or after hydrogenation will have number average molecular
weights in the order of about 10,000 to about 450,000, or from
about 35,000 to 150,000.
[0061] Also, prior to hydrogenation, the vinyl content of the
conjugated diene portion generally is from about 10% to about 80%,
or from about 25% to about 65%, particularly 35% to 55% when it is
desired that the modified block copolymer exhibit rubbery
elasticity. The vinyl content of the block copolymer can be
measured by means of nuclear magnetic resonance.
[0062] Specific examples of diblock copolymers include
styrene-butadiene (SB), styrene-isoprene (SI), and the hydrogenated
derivatives thereof. Examples of triblock polymers include
styrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),
alpha-methylstyrene-butadiene-alpha-methylstyrene, and
alpha-methylstyrene-isoprene alpha-methylstyrene. Examples of
commercially available block copolymers useful as the adhesives in
the present invention include those available from Kraton Polymers
LLC under the KRATON trade name.
[0063] Upon hydrogenation of the SBS copolymers comprising a
rubbery segment of a mixture of 1,4 and 1,2 isomers, a
styrene-ethylene-butylene styrene (SEBS) block copolymer is
obtained. Similarly, hydrogenation of an SIS polymer yields a
styrene-ethylene propylene-styrene (SEPS) block copolymer.
[0064] The selective hydrogenation of the block copolymers may be
carried out by a variety of well known processes including
hydrogenation in the presence of such catalysts as Raney nickel,
noble metals such as platinum, palladium, etc., and soluble
transition metal catalysts. Suitable hydrogenation processes which
can be used are those wherein the diene-containing polymer or
copolymer is dissolved in an inert hydrocarbon diluent such as
cyclohexane and hydrogenated by reaction with hydrogen in the
presence of a soluble hydrogenation catalyst. Such procedures are
described in U.S. Pat. Nos. 3,113,986 and 4,226,952, the
disclosures of which are incorporated herein by reference. Such
hydrogenation of the block copolymers which are carried out in a
manner and to extent as to produce selectively hydrogenated
copolymers having a residual unsaturation content in the polydiene
block of from about 0.5% to about 20% of their original
unsaturation content prior to hydrogenation.
[0065] In one embodiment, the conjugated diene portion of the block
copolymer is at least 90% saturated and more often at least 95%
saturated while the vinyl aromatic portion is not significantly
hydrogenated. Particularly useful hydrogenated block copolymers are
hydrogenated products of the block copolymers of
styrene-isoprene-styrene such as a
styrene-(ethylene/propylene)-styrene block polymer. When a
polystyrene-polybutadiene-polystyrene block copolymer is
hydrogenated, it is desirable that the 1,2-polybutadiene to
1,4-polybutadiene ratio in the polymer is from about 30:70 to about
70:30. When such a block copolymer is hydrogenated, the resulting
product resembles a regular copolymer block of ethylene and
1-butene (EB). As noted above, when the conjugated diene employed
as isoprene, the resulting hydrogenated product resembles a regular
copolymer block of ethylene and propylene (EP).
[0066] A number of selectively hydrogenated block copolymers are
available commercially from Kraton Polymers under the general trade
designation "Kraton G." One example is Kraton G1652 which is a
hydrogenated SBS triblock comprising about 30% by weight of styrene
end blocks and a midblock which is a copolymer of ethylene and
1-butene (EB). A lower molecular weight version of G1652 is
available under the designation Kraton G1650. Kraton G1651 is
another SEBS block copolymer which contains about 33% by weight of
styrene. Kraton G1657 is an SEBS diblock copolymer which contains
about 13% w styrene. This styrene content is lower than the styrene
content in Kraton G1650 and Kraton G1652.
[0067] In another embodiment, the selectively hydrogenated block
copolymer is of the formula:
B.sub.n(AB).sub.oA.sub.p
wherein n=0 or 1; o is 1 to 100; p is 0 or 1; each B prior to
hydrogenation is predominantly a polymerized conjugated diene
hydrocarbon block having a number average molecular weight of about
20,000 to about 450,000; each A is predominantly a polymerized
vinyl aromatic hydrocarbon block having a number average molecular
weight of from about 2000 to about 115,000; the blocks of A
constituting about 5% to about 95% by weight of the copolymer; and
the unsaturation of the block B is less than about 10% of the
original unsaturation. In other embodiments, the unsaturation of
block B is reduced upon hydrogenation to less than 5% of its
original value, and the average unsaturation of the hydrogenated
block copolymer is reduced to less than 20% of its original
value.
[0068] The block copolymers may also include functionalized
polymers such as may be obtained by reacting an alpha,
beta-olefinically unsaturated monocarboxylic or dicarboxylic acid
reagent onto selectively hydrogenated block copolymers of vinyl
aromatic hydrocarbons and conjugated dienes as described above. The
reaction of the carboxylic acid reagent in the graft block
copolymer can be effected in solutions or by a melt process in the
presence of a free radical initiator.
[0069] The preparation of various selectively hydrogenated block
copolymers of conjugated dienes and vinyl aromatic hydrocarbons
which have been grafted with a carboxylic acid reagent is described
in a number of patents including U.S. Pat. Nos. 4,578,429;
4,657,970; and 4,795,782, and the disclosures of these patents
relating to grafted selectively hydrogenated block copolymers of
conjugated dienes and vinyl aromatic compounds, and the preparation
of such compounds are hereby incorporated by reference. U.S. Pat.
No. 4,795,782 describes and gives examples of the preparation of
the grafted block copolymers by the solution process and the melt
process. U.S. Pat. No. 4,578,429 contains an example of grafting of
Kraton G1652 (SEBS) polymer with maleic anhydride with
2,5-dimethyl-2,5-di(t-butylperoxy) hexane by a melt reaction in a
twin screw extruder.
[0070] Examples of commercially available maleated selectively
hydrogenated copolymers of styrene and butadiene include Kraton
FG1901X, FG1921X, and FG1924X, often referred to as maleated
selectively hydrogenated SEBS copolymers. FG1901X contains about
1.7% w bound functionality as succinic anhydride and about 28% w of
styrene. FG1921X contains about 1% w of bound functionality as
succinic anhydride and 29% w of styrene. FG1924X contains about 13%
styrene and about 1% bound functionality as succinic anhydride.
[0071] Useful block copolymers also are available from Nippon Zeon
Co., 2-1, Marunochi, Chiyoda-ku, Tokyo, Japan. For example, Quintac
3530 is available from Nippon Zeon and is believed to be a linear
styrene-isoprene-styrene block copolymer.
[0072] Unsaturated elastomeric polymers and other polymers and
copolymers which are not inherently tacky can be rendered tacky
when compounded with an external tackifier. Tackifiers, are
generally hydrocarbon resins, wood resins, rosins, rosin
derivatives, and the like, which when present in concentrations
ranging from about 40% to about 90% by weight of the total adhesive
composition, or from about 45% to about 85% by weight, impart
pressure-sensitive adhesive characteristics to the elastomeric
polymer adhesive formulation. Compositions containing less than
about 40% by weight of tackifier additive do not generally show
sufficient "quickstick," or initial adhesion, to function as a
pressure-sensitive adhesive, and therefore are not inherently
tacky. Compositions with too high a concentration of tackifying
additive, on the other hand, generally show too little cohesive
strength to work properly in most intended use applications of
constructions made in accordance with the instant invention.
[0073] It is contemplated that any tackifier known by those of
skill in the art to be compatible with elastomeric polymer
compositions may be used with the present embodiment of the
invention. One such tackifier, found useful is Wingtak 10, a
synthetic polyterpene resin that is liquid at room temperature, and
sold by the Goodyear Tire and Rubber Company of Akron, Ohio.
Wingtak 95 is a synthetic tackifier resin also available from
Goodyear that comprises predominantly a polymer derived from
piperylene and isoprene. Other suitable tackifying additives may
include Escorez 1310, an aliphatic hydrocarbon resin, and Escorez
2596, a C.sub.5-C.sub.9 (aromatic modified aliphatic) resin, both
manufactured by Exxon of Irving, Tex. Of course, as can be
appreciated by those of skill in the art, a variety of different
tackifying additives may be used to practice the present
invention.
[0074] In addition to the tackifiers, other additives may be
included in the PSAs to impart desired properties. For example,
plasticizers may be included, and they are known to decrease the
glass transition temperature of an adhesive composition containing
elastomeric polymers. An example of a useful plasticizer is
Shellflex 371, a naphthenic processing oil available from Shell
Lubricants of Texas. Antioxidants also may be included on the
adhesive compositions. Suitable antioxidants include Irgafos 168
and Irganox 565 available from Ciba-Geigy, Hawthorne, N.Y. Cutting
agents such as waxes and surfactants also may be included in the
adhesives.
[0075] The pressure sensitive adhesive may be applied from a
solvent, emulsion or suspension, or as a hot melt. The adhesive may
be applied to the inner surface of the shrink film by any known
method. For example, the adhesive may be applied by die coating
curtain coating, spraying, dipping, rolling, gravure or
flexographic techniques. The adhesive may be applied to the shrink
film in a continuous layer, a discontinuous layer or in a pattern.
The pattern coated adhesive layer substantially covers the entire
inner surface of the film. As used herein, "substantially covers"
is intended to mean the pattern in continuous over the film
surface, and is not intended to include adhesive applied only in a
strip along the leading or trailing edges of the film or as a "spot
weld" on the film.
[0076] In one embodiment, an adhesive deadener is applied to
portions of the adhesive layer to allow the label to adhere to
complex shaped articles. In one embodiment, non-adhesive material
such as ink dots or microbeads are applied to at least a portion of
the adhesive surface to allow the adhesive layer to slide on the
surface of the article as the label is being applied and/or to
allow air trapped at the interface between the label and the
article to escape.
[0077] A single layer of adhesive may be used or multiple adhesive
layers may be used. Depending on the shrink film used and the
article or container to which the label is to be applied, it may be
desirable to use a first adhesive layer adjacent to the shrink film
and a second adhesive layer having a different composition on the
surface to be applied to the article or container for sufficient
tack, peel strength and shear strength.
[0078] In one embodiment, the pressure sensitive adhesive has
sufficient shear or cohesive strength to prevent excessive
shrink-back of the label where adhered to the article upon the
action of heat after placement of the label on the article,
sufficient peel strength to prevent the film from label from
lifting from the article and sufficient tack or grab to enable
adequate attachment of the label to the article during the labeling
operation. In one embodiment, the adhesive moves with the label as
the shrink film shrinks upon the application of heat. In another
embodiment, the adhesive holds the label in position so that as the
shrink film shrinks, the label does not move.
[0079] The heat shrinkable film may include other layers in
addition to the monolayer or multilayer heat shrinkable polymeric
film. In one embodiment, a metalized coating of a thin metal film
is deposited on the surface of the polymeric film. The heat
shrinkable film may also include a print layer on the polymer film.
The print layer may be positioned between the heat shrink layer and
the adhesive layer, or the print layer may be on the outer surface
of the shrink layer. In one embodiment, the film is reverse printed
with a design, image or text so that the print side of the skin is
in direct contact with the container to which the film is applied.
In this embodiment, the film is transparent.
[0080] The labels of the present invention may also contain a layer
of an ink-receptive composition that enhances the printability of
the polymeric shrink layer or metal layer if present, and the
quality of the print layer thus obtained. A variety of such
compositions are known in the art, and these compositions generally
include a binder and a pigment, such as silica or talc, dispersed
in the binder. The presence of the pigment decreases the drying
time of some inks. Such ink-receptive compositions are described in
U.S. Pat. No. 6,153,288 (Shih et al) and the disclosure of this
patent is hereby incorporated by reference.
[0081] The print layer may be an ink or graphics layer, and the
print layer may be a mono-colored or multi-colored print layer
depending on the printed message and/or the intended pictorial
design. These include variable imprinted data such as serial
numbers, bar codes, trademarks, etc. The thickness of the print
layer is typically in the range of about 0.5 to about 10 microns,
and in one embodiment about 1 to about 5 microns, and in another
embodiment about 3 microns. The inks used in the print layer
include commercially available water-based, solvent-based or
radiation-curable inks. Examples of these inks include Sun Sheen (a
product of Sun Chemical identified as an alcohol dilutable
polyamide ink), Suntex MP (a product of Sun Chemical identified as
a solvent-based ink formulated for surface printing acrylic coated
substrates, PVDC coated substrates and polyolefin films), X-Cel (a
product of Water Ink Technologies identified as a water-based film
ink for printing film substrates), Uvilith AR-109 Rubine Red (a
product of Daw Ink identified as a UV ink) and CLA91598F (a product
of Sun Chemical identified as a multibond black solvent-based
ink).
[0082] In one embodiment, the print layer comprises a
polyester/vinyl ink, a polyamide ink, an acrylic ink and/or a
polyester ink. The print layer may be formed in the conventional
manner by, for example, gravure, flexographic or UV flexographic
printing or the like, an ink composition comprising a resin of the
type described above, a suitable pigment or dye and one or more
suitable volatile solvents onto one or more desired areas of the
film. After application of the ink composition, the volatile
solvent component(s) of the ink composition evaporate(s), leaving
only the non-volatile ink components to form the print layer.
[0083] The adhesion of the ink to the surface of the polymeric
shrink film or metal layer if present can be improved, if
necessary, by techniques well known to those skilled in the art.
For example, as mentioned above, an ink primer or other ink
adhesion promoter can be applied to the metal layer or the
polymeric film layer before application of the ink. Alternatively
the surface of the polymeric film can be corona treated or flame
treated to improve the adhesion of the ink to the polymeric film
layer.
[0084] Useful ink primers may be transparent or opaque and the
primers may be solvent based or water-based. In one embodiment, the
primers are radiation curable (e.g., UV). The ink primer may
comprise a lacquer and a diluent. The lacquer may be comprised of
one or more polyolefins, polyamides, polyesters, polyester
copolymers, polyurethanes, polysulfones, polyvinylidine chloride,
styrene-maleic anhydride copolymers, styrene-acrylonitrile
copolymers, ionomers based on sodium or zinc salts or ethylene
methacrylic acid, polymethyl methacrylates, acrylic polymers and
copolymers, polycarbonates, polyacrylonitriles, ethylene-vinyl
acetate copolymers, and mixtures of two or more thereof. Examples
of the diluents that can be used include alcohols such as ethanol,
isopropanol and butanol; esters such as ethyl acetate, propyl
acetate and butyl acetate; aromatic hydrocarbons such as toluene
and xylene; ketones such as acetone and methyl ethyl ketone;
aliphatic hydrocarbons such as heptane; and mixtures thereof. The
ratio of lacquer to diluent is dependent on the viscosity required
for application of the ink primer, the selection of such viscosity
being within the skill of the art. The ink primer layer may have a
thickness of from about 1 to about 4 microns or from about 1.5 to
about 3 microns.
[0085] A transparent polymer protective topcoat or overcoat layer
may be present in the labels of the invention. The protective
topcoat or overcoat layer provide desirable properties to the label
before and after the label is affixed to a substrate such as a
container. The presence of a transparent topcoat layer over the
print layer may, in some embodiments provide additional properties
such as antistatic properties stiffness and/or weatherability, and
the topcoat may protect the print layer from, e.g., weather, sun,
abrasion, moisture, water, etc. The transparent topcoat layer can
enhance the properties of the underlying print layer to provide a
glossier and richer image. The protective transparent protective
layer may also be designed to be abrasion resistant, radiation
resistant (e.g, UV), chemically resistant, thermally resistant
thereby protecting the label and, particularly the print layer from
degradation from such causes. The protective overcoat may also
contain antistatic agents, or anti-block agents to provide for
easier handling when the labels are being applied to containers at
high speeds. The protective layer may be applied to the print layer
by techniques known to those skilled in the art. The polymer film
may be deposited from a solution, applied as a preformed film
(laminated to the print layer), etc.
[0086] When a transparent topcoat or overcoat layer is present, it
may have a single layer or a multilayered structure. The thickness
of the protective layer is generally in the range of about 12.5 to
about 125 microns, and in one embodiment about 25 to about 75
microns. Examples of the topcoat layers are described in U.S. Pat.
No. 6,106,982 which is incorporated herein by reference.
[0087] The protective layer may comprise polyolefins, thermoplastic
polymers of ethylene and propylene, polyesters, polyurethanes,
polyacryls, polymethacryls, epoxy, vinyl acetate homopolymers, co-
or terpolymers, ionomers, and mixtures thereof.
[0088] The transparent protective layer may contain UV light
absorbers and/or other light stabilizers. Among the UV light
absorbers that are useful are the hindered amine absorbers
available from Ciba Specialty Chemical under the trade designations
"Tinuvin". The light stabilizers that can be used include the
hindered amine light stabilizers available from Ciba Specialty
Chemical under the trade designations Tinuvin 111, Tinuvin 123,
(bis-(1-octyloxy-2,2,6,6-tetramethyl-4-piperidinyl) sebacate;
Tinuvin 622, (a dimethyl succinate polymer with
4-hydroxy-2,2,6,6-tetramethyl-1-piperidniethanol); Tinuvin 770
(bis-(2,2,6,6-tetramethyl-4-piperidinyl)-sebacate); and Tinuvin
783. Additional light stabilizers include the hindered amine light
stabilizers available from Ciba Specialty Chemical under the trade
designation "Chemassorb", especially Chemassorb 119 and Chemassorb
944. The concentration of the UV light absorber and/or light
stabilizer is in the range of up to about 2.5% by weight, and in
one embodiment about 0.05% to about 1% by weight.
[0089] The transparent protective layer may contain an antioxidant.
Any antioxidant useful in making thermoplastic films can be used.
These include the hindered phenols and the organo phosphites.
Examples include those available from Ciba Specialty Chemical under
the trade designations Irganox 1010, Irganox 1076 or Irgafos 168.
The concentration of the antioxidant in the thermoplastic film
composition may be in the range of up to about 2.5% by weight, and
in one embodiment about 0.05% to about 1% by weight.
[0090] A release liner may be adhered to the adhesive layer to
protect the adhesive layer during transport, storage and handling
prior to application of the label to a substrate. The release liner
may have an embossed surface and/or have non-adhesive material,
such as microbeads or printed ink dots, applied to the surface of
the liner.
Process
[0091] The process of applying the labels to articles or containers
involves non-traditional operations and equipment. The process
begins with traditional dispensing equipment that separates the
label from the release liner via a peel plate or tip that presents
the label with exposed adhesive to the container or article to be
decorated. Referring to FIGS. 6A to 6D, the label 62, which has a
central portion 61 and a peripheral portion 63 surrounding the
central portion and having an outer boundary defined by the label
edges, is contacted to the container 60 initially by applying
pressure to the label in the central portion. Having the initial
tack point(s) 64 located in a more central portion of the label
rather than on the leading edge or peripheral portion of the label
facilitates a more even distribution of any darts or wrinkles
formed between the leading and trailing edges of the applied label.
This in turn facilitates removal of the darts or wrinkles with the
application of heat.
[0092] For those articles having both compound curves and
relatively planar regions, the label may be initially contacted
with the container not on a compound curve, but closer to or within
a relatively planar area of the container surface.
[0093] Pressure is applied to the transferred label with a series
of brushes, rollers, wipers, squeegees, pneumatic rollers, or
walking beam in a center outward direction, as indicated by arrows
65, to obtain intimate contact between the label and the container
or article. This process is referred to herein as "wipe down" of
the label. The center to edge wiping motion forces any air trapped
beneath the label to the outer edges, as indicated by arrows 66,
and creates smaller, more evenly distributed darts at the edges of
the label. As the label covers the complex curves of the article,
excess label material accumulates in the form of darts, pleats,
channeling, bubbling and other application defects generally in the
peripheral portion of the label. Heat is applied to at least a
portion of the label to fully and smoothly adhere the label to the
container as shown in FIG. 6D.
[0094] In one embodiment, pressure is applied to the label using a
walking beam system equipped with a foam roller or foam covered
beam. The foam roller or beam applies downward pressure in the
longitudinal direction to the central region of the label and then
proceeds to the outer edges of the label, directing any air trapped
under the label and the pleats, wrinkles and/or other defects to
the outer edges of the label. This embodiment is illustrated in
FIGS. 7A and 7B, wherein container 70 having label 71 applied
thereto, is positioned on lower foam block 72a of a walking beam.
Upper foam block 72b applies downward pressure onto label 71 on
container 70 to push air from under the central portion of the
label to the periphery of the label as label and container are
compressed between the foam blocks of the walking beam.
[0095] Once the label is applied and initial wipe down is
completed, the excess label material darts and defects are
eliminated by heating at least a portion the label to shrink the
darts and/or wrinkles. The label may be heated via passage through
a heat tunnel, forced air, steam tunnel, direct contact heat pads
or forms. In one embodiment, the label is heated to a temperature
of at least 40.degree. C. In one embodiment, the label is heated to
at least 60.degree. C., or at least 70.degree. C., or at least
80.degree. C.
[0096] A subsequent wipe down of the label may be performed to
eliminate any remaining darts or wrinkles in the label. Pressure is
again applied to the label in a center outward direction to the
label. The second wipe down can be performed by a series of
rollers, wipers, squeegees, brushes, pneumatic rollers or a walking
beam. The subsequent wipe down may be performed concurrently with
the application of heat to the label, or subsequent to the
application of heat.
[0097] The labeled article of the present invention may be used in
a variety of applications, including, but not limited to personal
care products, household chemical products, food and beverages,
toys, electronics, pharmaceuticals, health care products,
industrial products and appliances.
EXAMPLES
[0098] The following examples are intended only to illustrate
methods and embodiments in accordance with the invention, and as
such should not be construed as imposing limitations upon the
claims.
Example 1
[0099] A pressure sensitive shrink label is constructed from a 3
mil thick low density polyethylene multilayer shrink film
designated CorrTuff from Sealed Air. The film is coated with an
acrylic emulsion adhesive S692N from Avery Dennison. The adhesive
is carried on a paper Glassine BG-40 silicone coated release liner.
The label is oversized, having the dimensions of approximately
5.times.3.5 inches, which is 20% greater than the industry standard
recommended label size for the bottle to which the label is
applied.
[0100] A 15 oz Johnson & Johnson Baby Lotion bottle having
compound curves is filled with water, capped and processed through
a Label-Aire 9000 series labeler at 100 bottles per minute (BPM).
The labeler has dual-feed screws with matched speed top and lower
belts with Label-Aire 2115-CD labeler heads with high torque
stepper motor drive. The labels are pressed down with a walking
beam type wipe down apparatus providing straight out, center
outward forces to direct the trapped air beneath the label and
resultant dart/pleat defects to the edge of the label. The
oversized label as applied to the bottle initially results in
unacceptable small darts and pleat defects around the perimeter of
the label. The labeled bottle is then processed through a Leister
hot forced air, conveyor wipe down system at 100 bpm. High velocity
260.degree. C. hot air heats the bottle and label to 50.degree. C.,
shrinking and taking up the excess label material darts and pleats
down to the bottle surface. The label is wiped down with a walking
beam for good label contact. The darts shrink and are easily wiped
flat after application of heat.
[0101] The finished labeled bottle with larger label area and
larger graphics content is smoothly wiped down without the darts,
pleats, ridges or wrinkle defects present in typical pressure
sensitive oversized labels. The darts do not return upon aging.
Table 1 below shows the properties of the label components.
Example 2
[0102] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 2 mil thick
polypropylene multilayer shrink film designated CZPA 200 from
Innovia is applied to the bottle having compound curves. After
initial wipe down, medium sized darts are formed. High velocity hot
air heats the bottle and label to 100.degree. C. The darts shrink
and are easily wiped flat after application of heat. The darts do
not return after aging.
Example 3
[0103] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 2 mil thick
polylactic acid single layer shrink film designated EARTHFIRST PLA
from Plastic Suppliers is applied to the bottle having compound
curves. After initial wipe down, medium sized darts are formed.
High velocity hot air heats the bottle and label to 70.degree. C.
The darts shrink and are easily wiped flat after application of
heat. The darts do not return after aging.
Comparative Example 4
[0104] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 2 mil thick
machine direction oriented polypropylene single layer
roll-on-shrink-on film from Avery Dennison is applied to the bottle
having compound curves. High velocity hot air heats the bottle and
label to 70.degree. C. The darts formed at the top and bottom of
the label shrink upon application of heat and are easily wiped
down, while the darts formed at the leading and trailing edges
remain. The removed darts do not return upon aging.
Comparative Example 5
[0105] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 1.9 mil thick
trans direction oriented polyvinyl chloride single layer film
designated Penta Label from Kloeckner is applied to the bottle
having compound curves. High velocity hot air heats the bottle and
label to 60.degree. C. The darts formed at the leading and trailing
edges of the label shrink upon application of heat and are easily
wiped down, while the darts formed at the top and bottom of the
label remain. The removed darts do not return upon aging.
Comparative Example 6
[0106] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 2 mil thick
trans direction oriented glycol modified polyethylene terephthalate
(PETG) single layer film designated Fusion 1775E from Mitsubishi is
applied to the bottle having compound curves. High velocity hot air
heats the bottle and label to 50.degree. C. The darts formed at the
leading and trailing edges of the label shrink upon application of
heat and are easily wiped down, while the darts formed at the top
and bottom of the label remain. The removed darts do not return
upon aging.
Comparative Example 7
[0107] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 1.4 mil thick
machine direction oriented polyvinyl chloride single layer film
designated MF-L243/01 from Kloechner is applied to the bottle
having compound curves. High velocity hot air heats the bottle and
label to 60.degree. C. The film does not conform to the container.
Initial wipe down is poor with many darts formed in all directions.
The darts and ridges remain after the application of heat and a
second wipe down. The film exhibits excessive shrink back.
Comparative Example 8
[0108] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 2.0 mil thick
polypropylene multilayer film designated BTNY from Vifan is applied
to the bottle having compound curves. High velocity hot air heats
the bottle and label to 100.degree. C. The darts formed do not
shrink completely at high temperature and do not entirely wipe down
flat. The darts return upon aging.
Comparative Example 9
[0109] In accordance with the process described in Example 1, a
pressure sensitive shrink label constructed from a 3.4 mil thick
medium density polyethylene (MDPE) multilayer film designated PE 85
from Charter Films is applied to the bottle having compound curves.
High velocity hot air heats the bottle and label to 100.degree. C.
The darts formed do not shrink completely at high temperature and
do not entirely wipe down flat. The darts return upon aging.
TABLE-US-00001 TABLE 1 L&W Film Ult Stiff- Poly- Construc-
Tensile Modulus ness Shrink: Shrink: Adhe- Ex. Grade mer tion
Process Suppliers Gauge (PSI) (PSI) (mN) MD TD sive Liner 1
CorrTuff LDPE single double Sealed Air 3.0 10,000 30,000 26 40% 49%
S692N BG40 layer bubble MD MD MD (106 C.) (106 C.) glassine 20,000
30,000 24 70% 69% CD CD CD (120 C.) (120 C.) 2 CZPA 200 PP multi-
double Innovia 2.0 20,000 100,000 24 10% 0% S692N 1.2 mil layer
bubble MD MD MD (106 C.) (106 C.) PET 22,000 130,000 18 14% 10% CD
CD CD (120 C.) (120 C.) 3 EARTHFIRST Poly single blown Plastic 2.0
8,000 300,000 44 7% 12% S692N 1.2 mil PLA Lactic layer Suppliers MD
MD MD (106 C.) (106 C.) PET Acid 8,000 300,000 60 8% 14% CD CD CD
(120 C.) (120 C.) Comp. Med Shrink PP single MDO Avery PPD 2.0 --
200,000 30 14% 0% S692N 1.2 mil 4 ROSO Film layer MD MD (106 C.)
(106 C.) PET 123,000 26 23% 0% CD CD (120 C.) (120 C.) Comp. Penta
Label PVC single TDO Kloeckner 1.9 7,200 -- 52 4% 56% S692N BG40 5
2.0 mil OT- layer MD MD (106 C.) (106 C.) glassine M276/41, 16,900
36 71/9400, CD CD GLGL Comp. Fusion 2.0 PETG single TDO Mitsubishi
2.0 7,250 -- 70 6% 66% S692N BG40 6 mil 1775E layer MD MD (106 C.)
(106 C.) glassine 29,000 30 CD CD Comp. MF- PVC single MDO
Kloechner 1.4 -- 220,000 -- 41% 0% S3506 1.2 mil 7 L243/01 layer MD
(106 C.) (106 C.) PET WHT 150,000 45% +3% 03/402-B CD (120 C.) (120
C.) Comp. BTNY PP multi- tenter Vifan 2.0 40,000 -- 35 2% 0% S692N
BG40 8 layer MD MD (106 C.) (106 C.) glassine 20,000 65 2% 2% CD CD
(120 C.) (120 C.) Comp. PE 85 MDPE multi- blown Charter 3.4 3,000
75,000 40 0% 0% S692N BG40 9 layer Films MD MD MD (106 C.) (106 C.)
glassine 3,500 60,000 50 4% 0% CD CD CD (120 C.) (120 C.)
[0110] While the invention has been explained in relation to its
preferred embodiments, it is to be understood that various
modifications thereof will become apparent to those skilled in the
art upon reading the specification. Therefore, it is to be under
stood that the invention disclosed herein is intended to cover such
modifications as fall within the scope of the appended claims.
* * * * *