Many attempts have been made to provide adhesive compositions which are particularly suitable for joining together layers of polymers, especially for joining structural polymers to polymers such as barrier resins. For example, Japanese Application 53 18653 discloses an adhesive resin for low temperature heat sealing purposes comprising 3 to 100 parts by weight of a hydrogenated petroleum resin, and 100 parts by weight of an ethylene carboxylate-vinyl acetate copolymer obtained by copolymerizing an unsaturated carboxylic acid and/or anhydride with at least one vinylidene monomer in the presence of an ethylene-vinyl acetate copolymer.

Japanese application 60 51768 discloses a hot melt adhesive composition of 100 parts by weight of polymer component, 25 to 200 parts by weight of tackifier resin, and 75 parts by weight or less of wax. The polymer component comprises 25 to 75 weight % low crystallinity or amorphous ethylene alpha-olefin copolymer (20 to 50 mole % ethylene, 50 to 80 mole % alpha-olefin) and 25 to 75 weight % ethylene vinyl ester copolymer. Either polymer, or both, are modified with unsaturated carboxylic acid or its acid anhydride. The tackifier resin is a terpene resin or petroleum resin. The wax is a paraffin, microcrystalline polyethylene, etc. The composition has a viscosity of 50 Pa.sec or less at 180 ^* c.

Japanese Application 01 27923 discloses a laminate in which a resin layer is coextrusion laminated onto an oriented film or Al foil. The adhesive is made of 50 to 99 weight percent ethylene-alpha-olefin random copolymer partially graft-modified with acid, and 1 to 50 weight percent tackifier. The ethylene-alpha-olefin copolymer has a density of 0.850 to 0.900 g/cc.

U.S. Patent 4,670,349 discloses an adhesive resin composition comprising 100 parts of an ethylene/vinyl acetate or ethylene/alpha-olefin random copolymer, 1-50 parts of modified polyethylene containing 0.01 to 10% grafted acid or derivative, and 1-125 parts hydrogenated aromatic petroleum resin. The resin composition is useful as an adhesive for polystyrene and ethylene vinyl alcohol copolymer.

U.S. Patent 4,337,297 discloses blends of a low density ethylene polymer and a copolymer of 70-90 % ethylene with the balance acrylic or methacrylic acid or vinyl acetate, the two ethylene polymers comprising together 100 parts; an ionomer resin having an acid content of 1-10%, 2-100 parts; and optionally a tackifying resin, 0-150 parts. The blend is a useful adhesive for PET film. U.S. Patent 4,367,113, Kari et al. discloses a similar blend except the low density polymer is replaced by an ethylene-alpha olefin copolymer or isotactic propylene polymer.

U.S. Patent 4,358,557 discloses a hot-melt adhesive comprising ethylene vinyl acetate copolymer, a tackifier resin selected from hydrocarbon resin, polyterpene resin or rosin ester, a paraffin wax and an aromatic hydrocarbon resin.

U.S. Patent 4,861,676 discloses a blend of ethylene copolymer, ethylene copolymer modified by

grafting with a comonomer containing pendant acid or acid derivative functionality, styrene polymer, and alicyclic resin modifier or stabilized rosin ester. The composition provides a useful adhesive, particularly for bonding polystyrene to barrier polymers.

U.S. Patent 4,861,677 discloses a blend of ethylene vinyl acetate copolymer, ethylene vinyl acetate copolymer modified by grafting with a comonomer containing pendant acid or acid derivative functionality, and impact-modified polystyrene. The composition provides a useful adhesive, particularly for bonding polystyrene to gas barrier polymers.

SUMMARY OF THE INVENTION The present invention provides an extrudable bonding resin composition consisting essentially of: (a) about 65 to about 99 percent by weight of an ethylene copolymer portion consisting essentially of (i) about 1 to 100 percent by weight of a copolymer of about 50 to about 80 weight percent ethylene and 20 to about 50 weight percent of at least one comonomer copolymerized therewith selected from the group consisting of unsaturated mono- or dicarboxylic acids of 2-20 carbon atoms, esters or salts of said unsaturated mono- or dicarboxylic acids, vinyl esters of saturated carboxylic acids where the acid group has 1-18 carbon atoms, and carbon monoxide, the carbon monoxide being present in an amount of 0 to about 30 weight percent; having grafted thereon side chains at least one comonomer unit in length, the comonomer units in said side chains being selected from the group consisting of ethylenically unsaturated mono-, di-, or polycarboxylic acids, ethylenically unsaturated carboxylic acid anhydrides, metal salts

and half-esters of such acids and anhydrides, and mixtures thereof, wherein the amount of said grafted comonomer units comprises about 0.03 to about 10 percent by weight of the total bonding resin composition, and

(ii) 0 to about 99 percent by weight of at least one copolymer of about 50 to about 80 weight percent ethylene and 20 to about 50 weight percent of at least one comonomer copolymerized therewith selected from the group consisting of unsaturated mono- or dicarboxylic acids of 2-20 carbon atoms, esters or salts of said unsaturated mono- or dicarboxylic acids, vinyl esters of saturated carboxylic acids where the acid group has 1-18 carbon atoms, and carbon monoxide, the carbon monoxide being present in an amount of 0 to about 30 weight percent, wherein the copolymer of (i) and each copolymer of (ii) contain at least one said copolymerized comonomer in common, the amount of each such common comonomer in each copolymer of (ii) being within about 10% of the amount of the corresponding comonomer in copolymer (i) , and the total amount of said copolymerized comonomers other than such common comonomers in any such copolymer being less than about ιo%; and

(b) about 1 to about 35 percent by weight of a tackifying resin.

The invention further provides a multiple layer structure comprising at least one structural layer, at least one barrier layer, and at least one bonding layer of the above extrudable bonding resin composition.

DETAILED DESCRIPTION OF THE INVENTION The extrudable bonding resin of the present invention comprises a blend of about 65 to about 99

percent by weight, preferably about 80 to about 95 percent by weight, of an ethylene copolymer component, and about 1 to about 35 weight percent of a tackifying resin. The ethylene copolymer component comprises an ethylene copolymer grafted with pendant acid or certain acid derivative functionality. This grafted copolymer may be blended, if desired, with additional ungrafted ethylene copolymer. Such blending may be desirable in order to minimize the amount of the relatively more expensive grafted material, while maintaining the excellent adhesive properties of the composition.

The grafted ethylene copolymer is present in amounts of about 1 to about 100, and preferably about 5 to about 50 percent by weight of the ethylene copolymer portion of the composition. This component is a copolymer containing about 20 to about 50, and preferably about 25 to about 30 weight percent copolymerized comonomer selected from the group consisting of unsaturated mono- or dicarboxylic acids of 2-20 carbon atoms, esters or salts of said unsaturated mono- or dicarboxylic acids, vinyl esters of saturated carboxylic acids where the acid group has 1-18 carbon atoms, and carbon monoxide, the carbon monoxide being present in an amount of 0 to about 30 weight percent. (The amount of carbon monoxide is limited only because it is believed that preparation of polymers containing more than about 30 weight percent carbon monoxide is not feasible due to problems of reactor fouling.) Vinyl acetate is a preferred comonomer, but methyl acrylate, n-butyl acrylate, and the like, optionally with carbon monoxide present as a third monomer, are also quite suitable. The balance of the copolymer is substantially copolymerized ethylene. Such copolymers

are prepared by the well-known addition polymerization processes. Onto this copolymer are grafted additional comonomer units of carboxylic acid or certain carboxylic acid derivative functionality to form short sidechains. (It is believed that when maleic anhydride is the graft comonomer, the sidechains are only one or at most two monomer units long.) The melt index of the resulting graft copolymer, as measured by ASTM D1238 Condition *E", should be about 0.5 to about 40. Outside of these ranges, processing becomes more difficult, and flow instabilities may result.

The grafting monomer is selected from the group consisting of ethylenically unsaturated mono-, di-, or polycarboxylic acids, ethylenically unsaturated carboxylic acid anhydrides, and metal salts and half-esters of such acids and anhydrides. Examples of the acids and anhydrides include acrylic acid, ethacrylic acid, maleic acid, fumaric acid, itaconic acid, crotonic acid, itaconic anhydride, maleic anhydride, and dimethyl maleic anhydride, and salts and half-esters thereof. Among the acids and anhydrides that are particularly useful are maleic anhydride and maleic acid.

The method for grafting of the comonomer onto the ethylene copolymer can be any of the processes which are well known in the art. For example, grafting can be carried out in the melt without a solvent, as disclosed in European Patent Application 0 266 994, incorporated herein by reference, or in solution or dispersion. Melt grafting can be done using a heated extruder, a Brabender™ or Banbury™ mixer or other internal mixers or kneading machines, roll mills, and the like. The grafting may be carried out in the presence of a

radical initiator such as a suitable organic peroxide, organic perester, or organic hydroperoxide. The graft copolymers are recovered by any method which separates or utilizes the graft polymer that is formed. Thus the graft copolymer can be recovered in the form of precipitated fluff, pellets, powders, and the like.

The amount of monomer grafted onto the ethylene copolymer is not particularly limiting, and may be as low as about 0.03 weight percent or as much as about 5 percent or even 10 percent, based on the weight of the grafted ethylene copolymer. The total amount of graft polymer in the total adhesive composition, however, is important, and should be between about 0.03 and about 10 weight percent of the total composition, in order to obtain superior adhesive and bonding properties.

The ungrafted ethylene copolymer component comprises at least one comonomer similar to that described above, but without the grafted comonomer. in order to achieve good peel strength in laminates prepared from the present adhesive, the comonomer of the ungrafted copolymer should be of a type and amount sufficiently similar to that of the grafted copolymer that the grafted and ungrafted copolymers have a suitable degree of compatibility. Such copolymers are normally compatible if they contain the same or closely chemically related monomers (except for the graft comonomer) and the amounts of such monomers in the two copolymers are similar. Specifically, the grafted copolymer and each of the ungrafted copolymers (if there is more than one) should contain at least one said copolymerized comonomer in common and the amount of each such common comonomer in the grafted copolymer and the ungrafted copolymer should be within about 10%, and preferably within about 5%, of each

other. Thus if the grafted copolymer is based on an ethylene polymer containing 30 weight % n-butyl acrylate, the ungrafted copolymer should contain between about 20 and about 40 weight percent n-butyl acrylate. Small amounts of additional comonomers may also be present in one or both copolymers, but in order to retain compatibility each copolymer should contain less than about 10% by weight of such comonomers that are not common to the other copolymer. Alternatively, closely similar comonomers, such as n-butyl acrylate and i-butyl acrylate could be interchanged while retaining compatibility. It is preferred that the graft copolymer be the same as the ungrafted copolymer, except for the presence of the grafted monomers. The melt index of the ungrafted copolymer should be about 0.05 to about 40.

The ungrafted copolymer component can be a single polymer or it can be more than one polymer, provided that the comonomer content of each such polymer is as described above, i.e., the polymers are mutually compatible. It has been sometimes found to be desirable that the ungrafted copolymer component be a mixture of two polymers having identical comonomer contents but having differing melt indices. For example, one copolymer can have a melt index of about 6 and a second can have a melt index of 25 or higher. The mixture of these polymers should have an overall melt index within the range of about 0.05 to about 40, as indicated. Use of such a mixture of copolymers provides ease in processability in, for example extrusion coating.

It is similarly to be understood that the use of more than one graft copolymer will fall within the scope of the present invention, provided that the

general principles of polymeric compatibility set forth herein are maintained.

The second major component of the present invention is a tackifying resin, which is present at about 1 to about 35 weight percent, preferably about 5 to about 20 weight percent of the composition. Suitable tackifying resins may be selected from the categories of:

(i) alicyclic or aliphatic hydrocarbon resins;

(ii) aromatic hydrocarbon resins; (iii) rosin and rosin derivatives; and (iv) terpene resins, or mixtures thereof. These tackifying resins will generally have a ring-and-ball softening temperature (ASTM E-2858T) of 0 to 150"C, preferably about 75 to about 140*C. The tackifying resins employed in the present invention are well known products available from commercial sources. Rosin tackifiers are described in the Kirk Othmer Encyclopedia of Chemical Technology. Interscience Publishers, Second Edition, Volume 17, pages 475-509. They include naturally occurring rosins and chemically modified rosin derivatives obtained by hydrogenation, dehydrogenation, isomerization, and the like. Rosin derivatives includes rosin esters and rosin acids. Rosin acids are typically derived from tall oil and can be mixtures of so called abietic types and primary types. Rosin esters are formed by esterifying rosin acid with a di-, tri-, or tetra-hydroxy alphatic alcohol such as ethylene glycol, propylene glycol, glycerine, or pentaerythritol. The terpene resins are generally prepared by the polymerization of terpene hydrocarbons in the presence of Friedel-Crafts catalysts at moderately low temperatures. Petroleum

resins, under which are classed aliphatic, alicyclic, and aromatic hydrocarbon resins, are described in the Kirk Oth er Encyclopedia of Chemical Technology. Interscience Publishers, Third Edition, Volume 12, page 852. They are generally prepared by polymerization of 4-10 carbon atom hydrocarbons by selected Friedel Crafts catalysts. Higher or lower hydrocarbons may also be present. The product may be further partially or fully hydrogenated. Suitable aromatic resins can be prepared from polymerization of alpha methyl styrene, vinyl toluene, and/or indene monomers.

In addition to the above mentioned components, the adhesive resin may contain small amounts of other materials commonly used and known in the art, such as antioxidants, stabilizers, slip additives, and fillers. The adhesive resin composition is prepared by blending the above described components by any suitable means, such as melt blending, extruding, etc. Further details are provided in the Examples which follow.

The composition of the present invention provides excellent adhesion to polyester and copolyester resins, vinyl chloride polymers, polycarbonates, polyethylenes, ethylene copolymers, iono ers, polystyrene, ethylene vinyl alcohol copolymer, polyamides, and the like. It also shows good adhesion to substrates such as aluminum foil. The adhesive is particularly useful for extrusion or coextrusion laminating structural and barrier polymers on to substrates such as polyester film, including multiple layer structures comprising at least two structural layers and at least one barrier layer. The structural layers may be of the same material or can be of different materials, e.g. one layer polyester

and a second layer ionomer or acid copolymer. The adhesive can be used without having to resort to use of a solvent-based primer to prepare the polymer film surface. The resulting composite structures are useful in packaging and other applications. Examples

Adhesive blends for the Examples shown in Table 1 were prepared by dry blending the ingredients in a polyethylene bag and subsequently melt blending at 210 to 230*C in a 28 or 53 mm Werner & Pfleiderer™ twin screw extruder with a vacuum port. Each of the blends, listed in the Table, also contained about 0.10 weight percent Irganox™ 1010 hindered polyphenol stabilizer (not separately reported in the Table) . For the extruded pellets, 0.3 weight percent Kemamide™ 20 was also added.

The adhesive properties of the blends were evaluated by measuring the peel strength of laminates prepared using a sheet of the adhesive between two layers of PET film. The layers of PET film were 12 micrometers (0.48 mils) thick; heat seal conditions were 210 ^β C, 0.8 seconds dwell time and 324 kPa (47 psig) applied pressure. Peel strength was measured by ASTM D 1876-72, modified in that the test was run at 305 mm/min, rather than 254 mm/min, and 3 to 6 duplicates of each sample were measured, rather than 10. The numbers are given as grams per 25 mm.

Comparative Examples Cl through C8 show poor peel strength because the acid polymer, which contains o% vinyl acetate comonomer, is used with a base resin containing 28% vinyl acetate. This is greater than the 10% difference in comonomer content between the ethylene polymer and its acid-modified ethylene polymer permitted in the present invention. In contrast, Examples 1 through 4 show good results

because the difference in comonomer content between the acid polymer and the base resin is less than 10%.

TABLE I

weight percent isobutyl acrylate and 10 weight percent methacrylic acid, melt index 10 dg/min, or a copolymer of ethylene with 28 weight percent vinyl acetate, grafted with 1.5 weight percent maleic anhydride, melt index 2.0 dg/min. c. P90 is Arkon P90, 100% hydrogenated Cg hydrocarbon resin, from Arakawa Chemical, having a Ring and Ball softening point ("R&B") of 90"C. P115 is a similar material, R&B 115-C.

The laminates in Table 2 were made in the same manner as in Table 1. Comparative Examples C9 and CIO are to be compared with Example 5. In Comparative Example C9, a low peel number is observed because no acid polymer is employed. In Comparative Example CIO, the comonomer difference between the acid polymer and base resin polymer is greater than 10%. Comparative Example Cll, which contains no tackifier resin, compares unfavorably to Example 16 which is identical in composition with the exception of the tackifier. Examples 15, 16, and 17 show that blends of otherwise identical or compatible copolymers of different melt indices can be used in place of a single copolymer.

The laminates in Table 3 were prepared in the same manner as described for the Examples in Table l. Comparative Examples C12 and C15 show poor results because the acrylate comonomer at 10% and vinyl ester comonomer at 9% respectively fall below the range of the present invention, i.e., 15 to 40 weight percent. Comparative Examples C13 and C14 give low peel numbers compared to Example 18 because the difference in comonomer content between acid-containing polymer and the base polymers is greater than 10%.

SUBSTITUTESHEET

Add t onal materials not dent f ed n Table I: E/28VA', in the second column, is identical to the first E/28VA except that its melt index is 25 dg/min. P125 is Arkon™ P125 100% hydrogenated Cg hydrocarbon resin, R&B 125° C. P140 is a comparable material, R&B 140- C.

M115 is Arkon™ M115 85% hydrogenated Cg hydrocarbon resin, R&B 115°C. M135 is a comparable material, R&B 135° C.

F-105 is Floral™ 105 65% hydrogenated rosin ester from Hercules, R&B 104° R3102 is Regalrez™ 3102, 30% hydrogenated hydrocarbon resin from Hercules

R&B 102 ^β C. R6108, a comparable resin, is 60% hydrogenated, R&B 108° C.

R1126 is 100% hydrogenated, R&B 126° C.

E/9VA - ethylene/9% vinyl acetate copolymer, melt index 7

E/9VA-g-1.5MAn - ethylene/9% vinyl acetate copolymer, melt index 1.2, grafted with 1.5 weight percent maleic anhydride E/28VA' ' - ethylene/28% vinyl acetate copolymer, melt index 43 E/20MA - ethylene/20% methyl acrylate copolymer, melt index 2 E/20MA-g-1.5MAn - ethylene/20% methyl acrylate copolymer, melt index 3.6, grafted with 1.5 weight percent maleic anhydride E/21MA/4EHM - ethylene/21% methyl acrylate/4% ethyl hydrogen maleate terpoly er E/30nBA/10CO - ethylene/30% n-butyl acrylate/10% CO terpolymer, melt index 5 E/nBA/CO-g-MAn - ethylene/30% n-butyl acrylate/10% CO terpolymer, melt index 4.7, grafted with 0.3 weight percent maleic anhydride

In Table 4, the multiple layer structures were made by coextrusion coating a layer of ionomer (ethylene methacrylic acid copolymer containing 15% methacrylic acid moieties, melt index 10 dg/min, 22% neutralized with zinc ions) , 23 micrometers thick, and a layer of adhesive onto corona-treated PET film, 12 micrometers thick. The adhesive blends were melted in a 63 mm extruder with barrel temperatures from 154 ^β C at the rear to 232"C at the front. The ionomer resin was melted in a 114 mm extruder with barrel temperatures from 177*C in the rear to 232*C at the front. Both melt streams were fed into a 107 cm (42 inch) die set at 232 ' C. The air gap was set at 16.5 centimeters. Line speed was 122 meters per minute.

Comparative Examples C17, C18, C22, C24 and C25 give poor results because the difference in vinyl ester comonomer content between the acid-containing polymer and the base polymer is greater than 10%. Comparative Example C19 compares unfavorably with Example 28 because it contains no tackifier. In Comparative Example C20, the acrylate comonomer content of the ethylene polymer is below 20 weight percent. Comparative Examples C21, C23 and C26 contain no acid polymers.

TABLE IV

High . i. Adhesive

E Copol. ^D Copol c Acid Copol Tackifier Thickness

Ex. _____* i_ Type % Type % urn

C17 46 46 E/15MAA ^a 8 (none) 18

C18 80 0 E/lOiBA/lOMAA 20 II 10.2

C19 90 0 E/28VA-g-1.5MAn 10 " 8

C20 0 0 E/lOiBA/lOMAA 100 " 9

C21 95 0 (none) 0 F-105 5 23

C22 75 0 E/lOiBA/lOMAA 20 P115 5 28

24 55 0 E/28VA-g-1.5MAn 40 R6108 5 20

25 60 15 " 20 " 5 20

26 40 15 " 30 P125 5 23

C23 80 15 (none) 0 R3102 5 18

C24 60 15 E/lOiBA/lOMAA 10 P90 15 15

C25 50 15 " 20 F-105 15 15

27 30 15 E/28VA-g-1.5MAn 40 P115 15 10

C26 85 0 (none) 0 R6108 15 18

C27 65 0 E/lOiBA/lOMAA 20 P90 15 10

28 55 0 E/28VA-g-1.5MAn 20 R3102 15 8

29 45 0 " 40 P125 15 10

30 45 0 » 40 " 15 8 a. Ethylene/15 wt.% methacrylic acid copolymer, melt i b. In each case the polymer was E/28VA, melt index 6. c. In each case the polymer was E/28VA, melt index 25. d. "Green" refers to peel testing conducted as soon as

"1 wk" and "4 wk" refer to peel testing conducted respectively after sample manufacture.

In Table 5, the multiple layer structures of Examples 31 and 32 were made by coextrusion coating a layer of ionomer (as described for the Examples of Table 4) , adhesive, a layer of ethylene vinyl alcohol copolymer containing 44 ol % ethylene, melt index 16, and adhesive onto PET film as described for the Examples of Table 4. The adhesive blends were melted in a 63 mm extruder with barrel temperatures from 154*C at the rear to 232*C at the front. The ionomer resin was melted in a 114 mm extruder with barrel temperatures from 177*C in the rear to 232"C at the front. The ethylene vinyl alcohol resin was melted in a 62.5 mm extruder with barrel temperatures from 177"C in the rear to 232*C at the front. The melt streams were fed into a feedblock in which the adhesive stream was split into two. The 1067 mm die was at 232*C. The air gap was set at 16.5 centimeters. Line speed was 122 meters per minute. Good adhesive strength is achieved in the structure.

The multiple layer structures of Examples 33-39 were made with several different substrates. The adhesive blends were melted in a 87.5 mm extruder with barrel temperatures from 180*C in the rear to 240 ^β C at the front. The ionomer and acid copolymer resins were melted in a 62.5 mm extruder with a similar temperature profile. The melt streams were were fed into a die with a slot width of 800 mm. The die was set at 240*C. The air gap was at 15 centimeters. Good bond strengths are obtained with different substrates.

The multiple layer structures of Examples 40-49 were prepared by coextrusion of an adhesive layer between a copolyester layer and an ethylene vinyl alcohol copolymer containing 30 mol% ethylene

moieties. The copolyester was a high melt viscosity copolyester of ethylene glycol copolymerized with about 86% terephthalic and about 14% isophthalic acid, further containing 0.4% comonomer moieties derived from trimellitic acid. The adhesive blends were melted at 160*C in a 25 mm extruder at 4-6 rpm. The copolyester was fed through a 37.5 mm extruder at 30-45 rpm at 240*C. The extrudate was cast onto chill rolls maintained at 60"C. The takeup speed of the sheet was 1.5 m/min. Good bonding is achieved to copolyester and ethylene vinyl alcohol copolymer with these compositions.

TABLE V

Ethylene High m.i. Adhesive % MAn Copol. ^a Copol. ^{b c} Tackifier Thickness in Peel Str.,g/25ram

Ex. % % Type % υm blend green 1 wk 6 wk Stucture ^e

31 65 0 R3102 15 7.6 0.3 583 674 PET/A/EV0H1/A/I0N 32 65 0 R6108 15 5.1 0.3 574 686 II 33 50 15 R3102 15 5 0.3 367 383 PET/A/I0N0MER2 34 50 15 II 15 10 0.3 567 633 II 35 50 15 15 5 0.3 450 483 36 50 15 15 10 0.3 717 783 37 50 15 R6108 15 25 0.3 d d PET/A/PET 38 50 15 R3102 15 5 0.3 d d PET/A/AC/Al foil 39 50 15 •I 15 10 0.3 d d II 40 50 15 P125 15 50 0.3 3230 P0LYESTER/A/EV0H2 41 45 0 II 15 65 0.6 3450 42 40 15 II 5 65 0.6 4722 43 50 15 R3102 15 70 0.3 4859 44 65 0 II 15 55 0.3 4812 45 30 15 II 15 55 0.6 4722 46 50 15 R3108 15 60 0.3 4812 47 60 15 II 5 60 0.3 1816 48 65 0 II 15 50 0.3 4903 49 55 0 II 15 55 0.6 5085 a E/28VA, mi 6 b ^~ . E/28VA, mi 25 c. E/28VA-g-1.5MAnh, mi 2. d. Could not sepa e Multilayer structures as indicated, where A = adhesive layer (from this Table) ; PET = polyethylene terephthalate film, 12 micrometers, corona treated

I0N0MER1 = ethylene/15% methacrylic acid copolymer, 22% zinc neutralized, 25 micromet IONOMER2 = ethylene/8.7% methacrylic acid copolymer, 18% zinc neutralized, MI = 16, 2 AC = ethylene/9% acrylic acid copolymer, melt index 10, 25 micrometers Al foil = aluminum foil, 20 micrometers thick.

EV0H1 = ethylene vinyl alcohol copolymer, 44 mol % ethylene, MI = 16 8 micrometers EV0H2 = ethylene vinyl alcohol copolymer, 30 mol % ethylene, MI = 3, 80-120 micromete POLYESTER = copolymer of iso-, terephthalic, and trimellitic acids, 185-405 micromete