[0001] The present invention relates to a laminate and to a method for its production.
[0002] It has been found difficult to produce laminates of linear polyesters such as polyethylene
terephthalate and vinyl chloride polymers since these two types of polymers do not
usually adhere well to each other, indeed polyethylene terephthalate is often used
as a release layer for sheets or films of vinyl chloride polymers.
[0003] This invention provides a well adhered laminate of a synthetic linear polyester and
a plasticised vinyl chloride polymer, the effective bonding between these two particular
polymers being promoted by an intermediary primer coating comprising a certain polymeric
composition.
[0004] According to the present invention there is provided a laminate comprising a layer
of a synthetic linear polyester, a plasticiser-free polymeric primer coating applied
to at least one surface of the polyester layer and comprising a cross-linked composition
comprising a polymer of at least one monomer selected from the esters of acrylic acid
and methacrylic acid, and at least one layer made from a plasticised vinyl chloride
polymer composition which is bonded to the linear polyester layer through the intermediary
of the primer coating.
[0005] According to another aspect of the invention there is provided a process for the
production of a laminate which comprises applying an aqueous or organic dispersion
of a polymeric primer composition to at least one surface of a layer of a synthetic
linear polyester, said primer composition comprising a plasticiser-free cross-linkable
composition comprising a polymer of at least one monomer selected from the esters
of acrylic acid and methacrylic acid, removing the dispersing medium and cross-linking
the primer composition, and bonding to one or both sides of the polyester layer, through
the intermediary of the primer coating so formed, a layer made from a plasticised
vinyl chloride polymer composition.
[0006] According to a further aspect of the invention there is provided the use of a plasticiser-free
cross-linkable composition, comprising a polymer of at least one monomer selected
from the esters of acrylic acid and methacrylic acid, for the production of a primer
coating for a layer of a synthetic linear polyester which coating acts, when cross-linked,
as an adhesion-promoting agent between the layer of polyester and a layer made of
a plasticised vinyl chloride polymer which is bonded thereto.
[0007] It is to be understood that the term "layer" embraces foils, films and sheets.
[0008] The polymer of the primer composition may be a homopolymer or a copolymer. The polymer
may optionally include a copolymerised component derived from acrylic acid and/or
methacrylic acid. Preferably the primer composition is cross-linked by virtue of the
inclusion therein of a condensation product of an amine, such as melamine, urea and
diazines or their derivatives, with formaldehyde, which may be alkylated.
[0009] The above defined primer coating promotes excellent adhesion between the linear polyester
layer and the plasticised vinyl chloride polymer layer. An example of a composition
used for the primer coating comprises a copolymer of ethyl acrylate, methyl methylacrylate
and methacrylamide, which has been cross-linked with an ethylated melamine/formaldehyde
condensation product. The primer composition is preferably cross-linked with the aid
of a suitable added cross-linking catalyst, e.g. ammonium chloride, ammonium nitrate,
ammonium thiocyanate, ammonium dihydrogen phosphate, ammonium sulphate, diammonium
hydrogen phosphate, para toluene sulphonic acid, maleic acid stabilised by reaction
with a base, or morpholinium para toluene sulphonate. The cross-linking is preferably
effected before the laminating operation begins. The primer coating may be applied
to the linear polyester layer from an aqueous or organic medium but preferably is
applied as an aqueous dispersion. The polyester layer bearing the dispersion should
be dried, preferably by heating to a temperature exceeding 70
0C and up to a maximum temperature determined by the nature of the polyester employed.
Heating not only serves to drive off the aqueous or organic medium but also to facilitate
the cross-linking reactions.
[0010] The primed polyester layer (before lamination) is not at all sticky and can be stored
(e.g. wound up in a roll) like an unprimed polyester film without any problems.
[0011] Examples of suitable synthetic linear polyesters which may be used for the laminates
of the invention include those polyesters which may be obtained by condensing one
or more dicarboxylic acids or their lower alkyl diesters, e.g. terephthalic acid,
isophthalic acid, phthalic acid, 2,5-, 2,6- and 2,7-naphthalene dicarboxylic acids,
succinic acid, sebacic acid, adipic acid, azelaic acid, diphenyl dicarboxylic acid,
and hexahydroterephthalic acid or bis-p-carboxylphenoxy ethane, and optionally a monocarboxylic
acid, such as pivalic acid, with one or more glycols, e.g. ethylene glycol, 1,3-propanediol,
1,4-butanediol, neopentyl glycol and 1,4-cyclohexanedimethanol. Biaxially oriented
and heat-set films or sheets of polyethylene terephthalate are particularly preferred
for the production of laminates according to the invention.
[0012] When the layer of the linear synthetic polyester is an oriented film, e.g. a biaxially
oriented film of polyethylene terephthalate, the primer coating composition may be
applied to the polyester layer before or between the stretching operations employed
to achieve orientation. A convenient procedure is to coat the polyester film between
the two stretching operations which are applied in mutually perpendicular directions
to orient the film. The heat treatment of the film during the stretching operation(s)
and heat setting serves also to remove the dispersing medium and to effect cross-linking.
[0013] Any suitable vinyl chloride polymer may be employed in the laminates of the invention.
By a vinyl chloride polymer, is meant a vinyl chloride homopolymer or a vinyl chloride
copolymer containing at least 50% molar (preferably at least 80% molar) of polymerised
vinyl chloride. The vinyl chloride polymer may be prepared by any suitable polymerisation
process, e.g. polymerisation in aqueous emulsion, suspension or microsuspension, or
in bulk, provided the properties (particularly the morphology) of the resulting polymer
are such that the polymer is suitable for use in the particular lamination procedure
envisaged.
[0014] The presence of the plasticiser in the vinyl chloride polymer layer is an essential
requirement for the achievement of a strong bond. The optimum amount or range of plasticiser
to be used for any particular laminate should be determined experimentally as this
depends, inter alia, on the minimum acceptable level of adhesion required, on the
type of plasticiser employed, on the nature of the linear polyester employed, on the
nature of the vinyl chloride polymer employed and on the method of bonding used to
form the laminate. However an amount of plasticiser within the range 20% to 120% by
weight based on the weight of the vinyl chloride polymer is usually acceptable for
most laminates. Suitable plasticisers for use in the laminates of the invention include
phthalate esters such as dioctyl phthalate, di-iso-octyl phthalate, C7-C9 alkyl phthalate
and butyl benzyl phthalate, phosphates such as tricresyl phosphate, carboxylic acid
esters such as di-iso-octyl adipate, di-2-ethylhexyl azelate and dioctyl sebacate,
compounds derived from soya bean oil such as epoxidised soya bean oil, liquid polyester
plasticisers such as polypropylene laurate and chlorinated substances such as the
chlorinated paraffins. The preferred plasticisers are the alkyl phthalates, particularly
dioctyl phthalate, di-iso-octyl phthalate, C7-C9 alkyl phthalate and butyl benzyl
phthalate.
[0015] The layer of plasticised vinyl chloride polymer may be incorporated into the laminate
of the invention by any suitable technique.
[0016] In one method a plastisol or an organosol derived from a vinyl chloride polymer (the
polymer normally being made by polymerisation in aqueous emulsion or microsuspension)
is spread onto a primed layer of a linear polyester and the assembly is heated to
gel the plastisol or (after removal of the diluent) the organosol into a coherent
layer. The heating may also cause the vinyl chloride polymer layer to become acceptably
bonded to the linear polyester layer. If the adhesion is insufficient, further heating
and/or pressure may be applied to effect a strong bond. Alternatively the plastisol
may be embossed. The plastisol in some cases may advantageously be foamable, so that
the plastisol fusing step also causes a foamed vinyl chloride polymer layer to be
formed.
[0017] In another method, a pre-formed plasticised film containing a plasticised vinyl chloride
polymer (the polymer normally being made by polymerisation in aqueous suspension,
microsuspension or emulsion) and a primed film of a linear polyester (usually polyethylene
terephthalate) are fed through hot rollers (provided e.g. by a calender) in order
to bond the polyester film to the plasticised vinyl chloride polymer film.
[0018] The laminates of the invention find uses in many applications. For example they may
form the basis of laminated cushioned flooring, the cushioned flooring comprising
e.g. a support polyethylene terephthalate film laminated on its lower side, through
the intermediary of a primer coating Cas defined), to a filled unfoamed plasticised
vinyl chloride polymer layer forming the base of the flooring Cthe filler e.g. being
a heat stabilised TiO
2 composition), and on its upper side, again through the intermediary of a primer coating
(as defined) to a foamed layer of a plasticised vinyl chloride polymer which has been
applied by spreading a plastisol as described above, the upper surface of the foam
being suitably patterned (e.g. by printing) and normally protected by a clear wear-resistant
layer.
[0019] The laminates of the invention may also be used as the basis of solid Ci.e. entirely
unfoamed) floor or wall tiles which comprise e.g. a filled plasticised vinyl chloride
base layer suitably patterned on its upper surface (e.g. by printing) and laminated,
through the intermediary of a primer coating (as defined), to a clear wear-resistant
layer of polyethylene terephthalate, the lamination being effected by calendering
the vinyl chloride layer (pre-formed) and the primed polyethylene terephthalate layer.
[0020] Another use for laminates of the invention is as protective, tamper-proof coverings
for identification cards such as security cards, bank cards, credit cards, identity
cards and the like. These can be prepared by covering the card on each surface with
facing polyester/ vinyl chloride polymer laminates according to the invention the
layers being in the form of flexible or stiff films) each laminate extending beyond
the card perimeter and the linear polyester layers of the laminates being outermost
and the plasticised vinyl chloride polymer layers being innermost, the assembly can
then be heat-sealed e.g. by passing it through hot rollers, the innermost plasticised
vinyl chloride polymer layers enabling each laminate to be bonded to the card and
also to the part of the opposite laminate which is beyond the perimeter of the card.
[0021] Another possible application for laminates according to the invention is their use
as cladding for various substrates, e.g. GRP sheet, where the linear polyester layer
improves the ageing performance of the substrate while the vinyl chloride polymer
layer (situated outermost) decreases the susceptibility of the polyester to degradation
by ultra-violet light.
[0022] Another use for laminates according to the invention is as adhesive tapes in packaging
and electrical applications where the laminated tapes replace those made solely from
vinyl chloride polymers which are known to suffer from poor transverse tensile strength.
The polyester layer (when biaxially oriented) significantly improves the transverse
tensile strength of the tape while the plasticised vinyl chloride layer enables a
very thin polyester layer (e.g. ~ 10-15 u) to be employed without detracting from
the tape's improved tensile properties
j a thick polyester tape would be economically less attractive. The plasticised vinyl
chloride polymer layer should also be very thin (e.g. -12-18 u) in order for the total
tape thickness to be acceptably thin, and so the lamination is preferably effected
by the application of an organosol of the vinyl chloride polymer to the primed polyester
film and (after removing the volatile diluent) gelling the organosol.
[0023] The present invention is further illustrated by the following description with reference
to the accompanying drawings in which:
Figure 1 is part of a cross-section of a laminate according to the invention.
Figure 2 is part of a cross-section of another laminate according to the invention.
Figure 3 is part of a cross-section of a laminate according to the invention in the
form of a solid floor or wall tile.
Figure 4 is part of a cross-section of a laminate according to the invention in the
form of a piece of cushion flooring.
[0024] It is to be understood that for the purpose of clear illustration, the drawings are
schematic, are not to scale, and have exaggerated features.
[0025] The laminate of Figure 1 has a plasticised film 1 of a vinyl chloride polymer bonded,
through the intermediary of a primer coating 2 according to the invention, to a biaxially
oriented film 3 of polyethylene terephthalate.
[0026] The laminate of Figure 2 consists of a foamed plasticised layer 4 of a vinyl chloride
polymer bonded, through the intermediary of a primer coating 5 according to the invention,
to a biaxially oriented film 6 of polyethylene terephthalate.
[0027] The solid floor or wall tile of Figure 3 consists of a base sheet 7 of a filled plasticised
vinyl chloride polymer bonded through the intermediary of a primer coating 8 according
to the invention to a wear-resistant biaxially oriented film 9 of polyethylene terephthalate.
The sheet 7 has a printed pattern, denoted by 10, on its upper side.
[0028] The cushioned flooring of Figure 4 consists of a biaxially oriented film 11 of polyethylene
terephthalate primed on each side with primer coatings 12 and 13 and bonded through
the intermediary of the primer coatings respectively to a base sheet 14 made from
a filled plasticised vinyl chloride polymer and to a foamed layer 15 made from a plasticised
vinyl chloride polymer. The foamed layer 15 has a printed pattern, denoted by 16,
on its upper side which is protected by a wear-resistant layer 17.
[0029] The present invention is further illustrated by the following Examples. Unless otherwise
specified, all parts and percentages are by weight.
EXAMPLE 1
[0030] A biaxially oriented film of polyethylene terephthalate was prepared by stretching
in mutually perpendicular directions at 90-95 C followed by heat-setting at about
210°C, after the first stretching operation the film was coated on one side with a
primer composition derived from an aqueous latex of 9.6 parts of a cross-linkable
acrylic composition consisting of 87% of a copolymer of ethyl acrylate, methyl methacrylate
and methacrylamide (45%, 50% and 5%) and 13% of ethylated melamine formaldehyde, 0.3
parts of poly(ethylene oxide - propylene oxide) emulsifier, 0.1 parts ammonium chloride
(catalyst) in 90 parts water, the heating during the second stretching operation and
heat setting serving to remove the water and cross-link the acrylic composition. The
film was coated on the primed side with a plastisol composition having the following
formulation:

[0031] The plastisol was produced by mixing the constituents in a planetary mixer and was
spread as a 3 mm thick layer on the coated polyethylene terephthalate film using knife-over-roll
coating. The coated assembly was passed through a circulating air oven at 190
0C for 3 minutes to fuse the plastisol and to generate a bond between the vinyl chloride
homopolymer and the polyethylene terephthalate film. The laminate was cooled and reeled.
[0032] The bond between the vinyl chloride homopolymer film and the polyethylene terephthalate
film was found to be very strong. The type of laminate formed is illustrated in Figure
1.
EXAMPLE 2
[0033] The procedure used was substantially that of Example 1. However the vinyl chloride
homopolymer plastisol employed was foamable and had the following formulation:

[0034] The assembly Chaving an unfoamed plastisol layer 1 mm thick) was heated at 195°C
for 3.5 minutes, producing a foamed vinyl chloride polymer layer 3.5 mm thick bonded
strongly to the polyethylene terephthalate film. The type of laminate formed is illustrated
in Figure 2.
EXAMPLE 3
[0035] The coated polyethylene terephthalate film as used in Examples 1 and 2 was used for
this Example. A calendered vinyl chloride copolymer sheet having the following formulation
was prepared:

[0036] This calendered sheet was press laminated (160°C, 4 minutes pressing) to the primed
polyethylene terephthalate film. The bond formed was very strong.
[0037] The type of laminate formed is illustrated in Figure 1 (with the vinyl chloride layer
being made from a calendered sheet and not from a plastisol as in
Example 1).
EXAMPLE 4
[0038] Cushion flooring of the type illustrated in Figure 4 was prepared, starting from
biaxially oriented polyethylene terephthalate film coated on both sides with the primer
composition used in Examples 1 to 3.
[0039] Firstly, a layer of filled unfoamed vinyl chloride polymer (e.g. made from the formulation
used in Example 1 or Example 3) was bonded to the polyester layer using any suitable
technique (plastisol spreading, calendering, pressing) so as to form the base of the
flooring. Next, a foamable plastisol derived from a vinyl chloride polymer (having
the formulation of the plastisol composition used in Example 2) was spread onto the
upper side of the primed polyester layer and foamed and gelled by heating. The cushion
flooring was suitably patterned by printing and finished with a wear-resistant layer.
1. A laminate comprising a layer of a synthetic linear polyester, a plasticiser-free
polymeric primer coating applied to at least one surface of the polyester layer and
comprising a cross-linked composition comprising a polymer of at least one monomer
selected from the esters of acrylic acid and methacrylic acid, and at least one layer
made from a plasticised vinyl chloride polymer composition which is bonded to the
linear polyester layer through the intermediary of the primer coating.
2. A laminate according to claim 1 wherein the polyester layer is biaxially oriented.
3. A laminate according to either claim 9 or claim 2 wherein the synthetic linear
polyester is polyethylene terephthalate.
4. A laminate according to any one of the preceding claims wherein the at least one
layer of the vinyl chloride polymer is foamed.
5. A process for the production of a laminate . which comprises applying an aqueous
or organic dispersion of a polymeric primer composition to at least one surface of
a layer of a synthetic linear polyester, said primer composition comprising a plasticiser-free
cross-linkable composition comprising a polymer of at least one monomer selected from
the esters of acrylic acid and methacrylic acid, removing the dispersing medium and
cross-linking the primer composition, and bonding to one or both sides of the polyester
layer, through the intermediary of the primer coating so formed, a layer made from
a plasticised vinyl chloride polymer composition.
6. A process according to claim 5 wherein the polyester layer is biaxially oriented
using stretching operations and the primer coating composition is applied to it before
or between the stretching operations.
7. A process according to either claim 5 or claim 6 wherein the layer of the plasticised
vinyl chloride polymer is derived from a plastisol or organosol of the vinyl chloride
polymer which is spread over the primer coating and the assembly heated to gel the
plastisol or (after removal of the organosol diluent) the organosol into a coherent
layer.
8. A process according to claim 7 wherein the plastisol is foamable so that the plastisol
gelling step also causes a foamed vinyl chloride polymer to be formed.
g. The use of a plasticiser-free cross-linkable composition comprising a polymer of
at least one monomer selected from the esters of acrylic acid and methacrylic acid,
for the production of a primer coating for a layer of a synthetic linear polyester
which coating acts, when cross-linked, as an adhesion-promoting agent between the
layer of polyester and a layer made of a plasticised vinyl chloride polymer which
is bonded thereto.
10. The use of a plasticiser-free cross-linkable composition according to claim 9
wherein the polymer of said composition is a copolymer of ethyl acrylate, methyl methacrylate
and methacrylamide.
11. The use of a plasticiser-free cross-linkable composition according to claim 9
wherein the polymer of said composition includes a copolymerised component derived
from acrylic acid and/or methacrylic acid.
12. The use of a plasticiser-free cross-linkable composition according to any one
of claims 9 to 11 wherein the cross-linking of the composition is effected by the
inclusion therein of a condensation product of an amine with formaldehyde.