Classifications

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• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31725—Of polyamide
  • Y10T428/3175—Next to addition polymer from unsaturated monomer[s]
  • Y10T428/31757—Polymer of monoethylenically unsaturated hydrocarbon
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
  • Y10T428/31797—Next to addition polymer from unsaturated monomers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/3188—Next to cellulosic
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31909—Next to second addition polymer from unsaturated monomers
  • Y10T428/31913—Monoolefin polymer
  • Y10T428/3192—Next to vinyl or vinylidene chloride polymer
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31935—Ester, halide or nitrile of addition polymer
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31938—Polymer of monoethylenically unsaturated hydrocarbon

Definitions

• safety laminates that comprise a crosslinkable polymeric interlayer sheet formed of compositions of ethylene copolymers, blends of ethylene copolymers, and ethylene copolymer/ionomer blends.
• Safety laminates have been in commercial production for almost a century and have been utilized in applications that require sheet material having a high degree of clarity and impact resistance.
• safety laminates have been widely used in the automobile industry as windshields or side windows because the laminate structures are characterized by high impact and penetration resistance and because they do not scatter glass shards and debris when shattered.
• safety laminates have also been incorporated into building structures as windows, walls, stairs, and the like.
• Simple safety laminates typically consist of a sandwich of two glass sheets or panels bonded together with an interlayer of a polymeric sheet. One or both of the glass sheets may be replaced with optically clear rigid polymeric sheets, such as sheets made of polycarbonate.
• Safety glass laminates have further evolved to include multiple layers of glass and polymeric sheets bonded together with interlayers of polymeric sheets.
• interlayers used in safety laminates are typically made from relatively thick polymer sheets, which exhibit toughness and bondability to the glass in the event of a crack or crash.
• Widely used interlayer materials include complex, multicomponent compositions based on polyvinyl butyral), poly(urethane), and ethylene vinyl acetate copolymers.
• lonomers are copolymers produced by partially or fully neutralizing the carboxylic acid groups of precursor or parent polymers that are acid copolymers comprising
• a safety laminate that comprises (A) at least one rigid sheet layer or at least one film layer; and (B) at least one polymeric interlayer comprising an Ethylene Copolymer 1 , or an Ethylene Copolymer 2, or a cross-linked or cross-linkable blend composition of Ethylene Copolymer 1 and Ethylene Copolymer 2, or a cross-linked or cross- linkable blend of Ethylene Copolymer 2 and an ionomer of Ethylene Copolymer 1.
• R 3 and R 4 represent hydrogen or an alkyl group
• R 2 represents an alkyl group
• D represents a moiety containing an epoxy group
• R 1 , R 3 and R 4 represent hydrogen or an alkyl group;
• R 2 represents an alkyl group;
• D represents a moiety containing an epoxy group.
• compositions, a process, a structure, or a portion of a composition, a process, or a structure is described herein using an open-ended term such as "comprising,” unless otherwise stated the description also includes an embodiment that "consists essentially of” or “consists of” the elements of the composition, the process, the structure, or the portion of the composition, the process, or the structure.
• substantially free refers to a composition that includes no more than an adventitious amount of the component. Stated alternatively, the composition includes no added amount of the component, only the amount that is commonly present in the raw materials from which the composition is produced. In some commercially available materials, the level of adventitious components is less than less than 2.5%, 1 .0%, less than 0.5%, or less than 0.1 % by weight, based on the weight of the commercially available material.
• ranges set forth herein include their endpoints unless expressly stated otherwise.
• an amount, concentration, or other value or parameter is given as a range, one or more preferred ranges or a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether such pairs are separately disclosed.
• the scope of the invention is not limited to the specific values recited when defining a range.
• melt flow rate MFR
• melt flow index MFI
• melt index Ml
• copolymer refers to polymers comprising copolymerized units resulting from copolymerization of two or more comonomers.
• a copolymer may be described herein with reference to its constituent comonomers or to the amounts of its constituent comonomers, for example "a copolymer comprising ethylene and
• dipolymer refers to polymers consisting essentially of two monomers, and the term “terpolymer” refers to polymers consisting essentially of three monomers.
• acid copolymer refers to a polymer comprising
• (meth)acrylic as used herein, alone or in combined form, such as
• (meth)acrylate refers to acrylic or methacrylic, for example, “acrylic acid or methacrylic acid”, or “alkyl acrylate or alkyl methacrylate”.
• epoxy group ethylene oxide group
• oxirane ring are synonymous and used interchangeably herein to refer to a substituted or unsubstituted group having the formula -CROCR 2 , wherein the oxygen atom is bound to both carbons and the carbons are bound to each other.
• R groups are hydrogen atoms
• the ethylene oxide group is unsubstituted.
• the ethylene oxide group may be singly or multiply substituted. Stated alternatively, one, two or three of the R groups may be other than hydrogen atoms.
• alkyl group and alkylene group as used herein alone or in combined form, such as, for example, “alkoxy group”, refer to saturated hydrocarbon groups that have from 1 to 8 carbon atoms and that may be branched or unbranched.
• An alkyl group has one bond to a carbon atom available for substitution, and an alkylene group has two bonds to one or more carbon atoms available for substitution.
• ionomer refers to a polymer that comprises ionic groups that are carboxylate salts, for example, ammonium carboxylates, alkali metal carboxylates, alkaline earth carboxylates, transition metal carboxylates and/or combinations of such carboxylates.
• carboxylate salts for example, ammonium carboxylates, alkali metal carboxylates, alkaline earth carboxylates, transition metal carboxylates and/or combinations of such carboxylates.
• Such polymers are generally produced by partially or fully neutralizing the carboxylic acid groups of precursor or parent polymers that are acid copolymers, as defined herein, for example by reaction with a base.
• an alkali metal ionomer as used herein is a sodium ionomer (or sodium neutralized mixed ionomer), for example a copolymer of ethylene and methacrylic acid wherein all or a portion of the carboxylic acid groups of the copolymerized methacrylic acid units are in the form of sodium carboxylate groups.
• a safety laminate comprising at least one rigid sheet layer or at least one film layer and at least one interlayer sheet, wherein the interlayer sheet comprises an ethylene copolymer composition.
• One safety laminate comprises a first ethylene copolymer (Ethylene Copolymer 1 ).
• Another safety laminate comprises a second ethylene copolymer (Ethylene Copolymer 2).
• Yet another safety laminate comprises a blend of Ethylene Copolymer 1 and Ethylene Copolymer 2.
• Yet another safety laminate comprises a blend of Ethylene Copolymer 1 and Ethylene Copolymer 2, wherein the blend is at least partially crosslinked.
• Ethylene Copolymer 1 is not an ionomer.
• the carboxylic acid groups of Ethylene Copolymer 1 are present in protonated form and no significant amount of these carboxylic acid groups is neutralized to form carboxylate salts.
• the Ethylene Copolymer 1 may optionally further comprise other suitable additional comonomers, such as unsaturated carboxylic acids having 2 to 10, or preferably 3 to 8 carbons, or derivatives thereof.
• suitable acid derivatives include acid anhydrides, amides, and esters. Esters are preferred. Specific examples of preferred esters of unsaturated carboxylic acids are described by Prejean. Examples of preferred comonomers include, but are not limited to, methyl (meth)acrylates, butyl (meth)acrylates, vinyl acetates, and combinations of two or more thereof.
• first olefin nor the second olefin nor the other suitable additional comonomer is a dicarboxylic acid or a diester, monoester or anhydride of a dicarboxylic acid.
• Dicarboxylic acids include maleic acid, fumaric acid, itaconic acid, citraconic acid, mesaconic acid, and the like.
• Ethylene Copolymer 1 preferably does not incorporate other comonomers in any significant amount.
• Ethylene Copolymer 1 consist essentially of copolymerized residues of ethylene and the second olefin, or that Ethylene Copolymer 1 consist essentially of copolymerized residues of ethylene, the optional first olefin and the second olefin.
• Ethylene Copolymer 1 further comprises up to about 30 wt%, or about 2 to about 30 wt%, or about 5 to about 20 wt%, or about 5 to about 15 wt%, based on the total weight of the copolymer, of
• Ethylene Copolymer 1 comprises copolymerized residues of ethylene and up to about 5 wt% of optional additional comonomers, if any. These weight percentages are based on the total weight of Ethylene Copolymer 1 .
• Ethylene Copolymer 1 has a melt flow rate or melt index (MFR or Ml) of about 5 g/10 min or higher, or about 30 g/10 min or higher, or about 30 to about 500 g/10 min, or about 60 g/10 min or higher, or about 60 to about 200 g/10 min, as determined in accordance with ASTM D1238 at 190°C and under a weight of 2.16 kg.
• MFR or Ml melt flow rate or melt index
• Ethylene Copolymer 1 is a copolymer of ethylene/n-butyl acrylate/acrylic acid, such as those available from E. I. du Pont de Nemours and Company, Wilmington, DE (“DuPont”) under the trademark Nucrel®.
• Ethylene Copolymer 1 may be an ionomer.
• at least a portion of the carboxylic acid groups of Ethylene Copolymer 1 may be neutralized to form carboxylate salts, lonomers and methods of synthesizing ionomers have been described at length elsewhere, for example in U.S. Patent No. 5,028,674, and U.S. Patent Appln. No.
• Preferred neutralization levels are up to about 90%, about 10% to about 90%, about 20% to about 60%, or about 15% to about 30%.
• Neutralization level is expressed as the weight percentage of the acid present in the ionomer that is neutralized. For example, if the ionomer contains 15 wt% of methacrylic acid and the neutralization level is 25%, then 3.75 wt% of the acid groups are neutralized, based on the total weight of the copolymer.
• Ethylene Copolymer 1 when neutralized has a melt flow rate or melt index (MFR or Ml) of about 1 g/10 min or higher, or about 5 to about 500 g/10 min, or about 10 to about 500 g/10 min, as determined in accordance with ASTM D1238 at 190°C and under a weight of 2.16 kg.
• MFR or Ml melt flow rate or melt index
• Ethylene Copolymer 1 is a zinc ionomer in which about 10% to about 90%, about 20% to about 60%, or about 15% to about 30% of the hydrogen atoms of the carboxylic acid groups of the precursor acid are replaced by a charge-equivalent amount of zinc cations.
• Ethylene Copolymer 1 is a zinc ionomer of a copolymer of ethylene/n-butyl acrylate/acrylic acid, such as those available from DuPont under the trademark Surlyn®.
• R 4 is hydrogen or an alkyl group
• D is selected -C0 2 R 5 , - C0 2 R 6 -R 5 , -R 6 -R
• the third olefin is also not a dicarboxylic acid or a di-ester, mono-ester or anhydride of a dicarboxylic acid.
• Ethylene Copolymer 2 may optionally further comprise other suitable additional comonomers, as described above with respect to Ethylene Copolymer 1 .
• Ethylene Copolymer 2 does not incorporate other comonomers in any significant amount. Stated alternatively, it is preferable that Ethylene Copolymer 2 consist essentially of copolymerized residues of ethylene and the third olefin, or that Ethylene Copolymer 2 consist essentially of copolymerized residues of ethylene, the optional first olefin and the third olefin.
• Ethylene Copolymer 1 may be a copolymer of ethylene/n-butyl acrylate/acrylic acid and Ethylene Copolymer 2 may be a copolymer of ethylene/n-butyl acrylate/glycidyl methacrylate.
• Ethylene Copolymer 1 may be a copolymer of ethylene/n-butyl acrylate/acrylic acid
• Ethylene Copolymer 2 may be a copolymer of ethylene/n-butyl acrylate/glycidyl methacrylate.
• Ethylene Copolymer 1 may be a copolymer of ethylene/n-butyl acrylate/acrylic acid
• Ethylene Copolymer 2 may be a copolymer of ethylene/n-butyl acrylate/glycidyl methacrylate.
• Copolymer 1 may be a copolymer of ethylene/methyl acrylate/acrylic acid and Ethylene Copolymer 2 may be a copolymer of ethylene/ethyl acrylate/glycidyl methacrylate.
• Ethylene Copolymer 2 comprises copolymerized residues of ethylene and up to about 5 wt% of optional additional comonomers, if any.
• Ethylene Copolymer 2 consists essentially of copolymerized residues of ethylene and the third olefin. Also preferably, Ethylene Copolymer 2 consists essentially of copolymerized residues of ethylene, the optional first olefin and the third olefin. In one particular example, the Ethylene Copolymer 2 is a copolymer of ethylene/n-butyl
• Ethylene Copolymer 2 is a copolymer of ethylene and glycidyl methacrylate.
• Ethylene Copolymer 2 has a melt flow rate of about 5 to about 300 or about 5 to about 100 g/10 min, as determined in accordance with ASTM D1238 at 190°C and under a weight of 2.16 kg.
• the ratio of the Ethylene Copolymer 1 and the Ethylene Copolymer 2 in the blend composition ranges from about 90:10 to about 10:90, or about 80:20 to about 20:80, or about 70:30 to about 30:70, or about 60:40 to about 40:60, or about 45:55 to 55:45, or the ratio is about 50:50 by weight based on the total weight of Ethylene Copolymer 1 and Ethylene Copolymer 2 in the blend composition.
• the mole ratio of carboxylic acid and carboxylate groups in Ethylene Copolymer 1 to epoxy groups in Ethylene Copolymer 2 is preferably about 10:1 to 1 :10, about 5:1 to 1 :5, about 3:1 to 1 :3, or about 2 to 1.
• the blend composition of Ethylene Copolymer 1 and Ethylene Copolymer 2 can be prepared by any suitable process, such as melt blending, compounding, and extrusion to pelletized blend.
• no water, no other solvents such as organic solvents and aromatic solvents, and no plasticizers are added to Ethylene Copolymer 1 and Ethylene Copolymer 2 during the blending process.
• neat Ethylene Copolymer 1 is combined with neat Ethylene Copolymer 2 in a melt process to form a neat blend composition.
• Ethylene Copolymers 1 and 2 include more than adventitious amounts of water, other solvent, or plasticizer.
• the temperature of the blend is preferably maintained at or below about 135°C, to prevent premature cross-linking. More preferably, the temperature of the blend is maintained at or below about 130°C, 125°C or 120°C. At temperatures of about 120°C or higher, the carboxylic acid group in Ethylene Copolymer 1 reacts with the epoxy group in Ethylene Copolymer 2 to form a blend composition that is cross-linked. In the case of a blend of an ionomer of Ethylene
• Copolymer 1 reacts with the epoxy group in Ethylene Copolymer 2, the reaction
• temperatures are slightly lower. Therefore, it is preferable to maintain the temperature of the blend at or below about 120°C, to prevent premature cross-linking. More preferably, the temperature of the blend is maintained at or below about 1 15°C, 1 10°C or 100°C. At temperatures of about 100°C or higher, the carboxylate group in ionomeric Ethylene Copolymer 1 reacts with the epoxy group in Ethylene Copolymer 2 to form a blend composition that is cross-linked.
• the cross-linking reaction between an ionomer comprising acrylic acid residues and a copolymer comprising residues of glycidyl methacrylate operates by a mechanism in which some of the carboxylic acid groups and carboxylate groups of the ionomer react to open epoxide rings, thus forming a beta-hydroxyalkyl ester linkage.
• the cross-linking reaction of a non-ionomeric blend may well proceed at temperatures that are below 135°C, or below 120°C.
• those of skill in the art are able to determine an appropriate level of cross-linking based on the physical properties that are desired in the cross-linked encapsulant layer. For example, higher levels of cross-linking are correlated with a higher flex modulus, better high temperature adhesion, lower melt indices, and better heat resistance.
• the interplay of synthetic factors such as reaction time and temperature, reagent concentration, and catalyst type and level is described in detail by Prejean.
• one preferred catalyst is 2-ethyl imidazole.
• a preferred amount of 2-ethyl imidazole is 200 to 1500 ppm, based on the total amount of the ethylene copolymer blend.
• the ethylene copolymer composition described herein may further contain any suitable additive known in the art.
• additives include, but are not limited to, plasticizers, processing aides, flow enhancing additives, flow reducing additives (e.g., organic peroxides), lubricants, pigments, dyes, optical brighteners, flame retardants, impact modifiers, nucleating agents, antiblocking agents (e.g., silica), thermal stabilizers, hindered amine light stabilizers (HALS), UV absorbers, UV stabilizers, dispersants, surfactants, chelating agents, coupling agents, adhesives, primers, reinforcement additives (e.g., glass fiber), fillers, and the like, and mixtures or combinations of two or more conventional additives.
• plasticizers e.g., processing aides, flow enhancing additives, flow reducing additives (e.g., organic peroxides), lubricants, pigments, dyes, optical brighteners, flame retardants, impact modifiers,
• ethylene copolymer composition is an un-ionized blend of Ethylene Copolymer 1 and Ethylene Copolymer 2, however, plasticizers are not suitable additives. These additives are described in the Kirk Othmer Encyclopedia of Chemical Technology, 5 th Edition, John Wiley & Sons (New Jersey, 2004), for example.
• these conventional ingredients may be present in the compositions in quantities of about 0.01 to about 15 wt%, or about 0.01 to about 10 wt%, so long as they do not detract from the basic and novel characteristics of the composition and do not significantly adversely affect the performance of the composition or of the articles prepared from the composition.
• the weight percentages of such additives are not included in the total weight percentages of the ionomer compositions defined herein. ⁇
• such additives may be present in amounts of about 0.01 to about 5 wt%, based on the total weight of the ionomer composition.
• a fourth notable additive is a silane coupling agent, which may be added to the ethylene copolymer composition to improve its adhesive strength.
• suitable silane coupling agents include, but are not limited to, ⁇ -chloropropylmethoxysilane, vinyltrimethoxysilane,
• vinyltriethoxysilane vinyltris(3-methoxyethoxy)silane,Y-vinylbenzylpropyl-trimethoxysilane, N-3-(N-vinylbenzylaminoethyl)-Y-aminopropyltrimethoxy-silane, ⁇ -methacryloxypropyl- trimethoxysilane, vinyltriacetoxysilane, ⁇ -glycidoxypropyl-trimethoxysilane, v- glycidoxypropyltriethoxysilane, 3-(3,4-epoxycyclohexyl)-ethyltrimethoxysilane,
• silane coupling agents may be incorporated in the ethylene copolymer composition at a level of about 0.01 to about 5 wt%, or about 0.05 to about 1 wt%, based on the total weight of the sodium/zinc mixed ionomer composition.
• the optional incorporation of such conventional ingredients into the ethylene copolymer compositions can be carried out by any known process. This incorporation can be carried out, for example, by dry blending, by extruding a combination of the various constituents, by a masterbatch technique, or the like. See, again, the Kirk-Othmer
• the melt from which the sheet is formed consists essentially of Ethylene Copolymer 1 , Ethylene Copolymer 2, and optional additives, if any.
• the melt is substantially free of solvents, including water and organic solvents. More preferably, the melt is substantially free of solvents and plasticizers.
• pellets or powders of neat Ethylene Copolymers 1 and 2 may be provided. These neat powders or pellets may be combined in a "salt and pepper" blend before melting. Alternatively, Ethylene Copolymers 1 and 2 may be pre-mixed to form pellets of the blend composition. These pellets are then melted in preparation for the extrusion process. The additives may be added to the pellets or powders before, during, or after melting.
• the temperature of the ethylene copolymer blend should be maintained at or below about 120°C, 1 15°C, 1 10°C, 105°C or 100°C (even lower for ionomeric blends), to avoid premature cross-linking.
• the temperature of the melt is held at or below about 120°C and the temperature at the extrusion die is about 135°C or higher. Exposure of the unreacted blend composition to higher temperatures for short periods of time is not expected to generate an unacceptable amount of premature cross-linking.
• the polymeric interlayer it may have a single layer or multilayer form.
• single layer it is meant that the sheet is made of or consists essentially of the ethylene copolymer composition disclosed herein.
• the other sub-layer(s) may be made of any other suitable polymeric material(s), such as, for example, acid copolymers as previously defined herein, ionomers as previously defined herein, ethylene/vinyl acetate copolymers, polyvinyl acetals) (including acoustic grade polyvinyl acetals)), polyurethanes, polyvinylchlorides, polyethylenes (e.g., linear low density polyethylenes), polyolefin block elastomers, copolymers of oolefins and ⁇
• the sheet comprising the ethylene copolymer composition may have a smooth or rough surface on one or both sides to facilitate deaeration during the lamination process.
• Rough surfaces can be created by known processes such as mechanical embossing or by melt fracture during extrusion of the sheets, or by processes described in, e.g., U.S. Patent No. 4,035,549 and U.S. Patent Publication No. 2003/0124296.
• the interlayer sheets comprising the ethylene copolymer compositions may be produced by any suitable process.
• the sheets may be formed through dipcoating, solution casting, compression molding, injection molding, lamination, melt extrusion, blown film, extrusion coating, tandem extrusion coating, or by any other procedures that are known to those of skill in the art.
• the sheets may be formed by melt extrusion, melt coextrusion, melt extrusion coating, blown film process, or tandem melt extrusion coating processes.
• One preferred safety laminate comprises at least one interlayer sheet comprising the ionomer composition, and the interlayer sheet is laminated to at least one rigid sheet or film layer.
• laminated it is meant that, within a laminated structure, the two layers are adhered or bonded either directly (that is, without any additional material between the two layers) or indirectly (that is, with additional material, such as interlayer or adhesive materials, between the two layers).
• Suitable rigid sheets comprise a material with a modulus of about 100,000 psi (690 MPa) or greater (as measured by ASTM Method D-638).
• the rigid sheets used here may be formed of glass, metal, ceramic, or of polymers including polycarbonates, acrylics, polyacrylates, cyclic polyolefins, polystyrene prepared in the presence of metallocene catalysts, and combinations of two or more thereof.
• Other suitable rigid sheets are described in U.S. Provisional Appln. No. 61/141 ,836, filed on December 31 , 2008 (Attorney Docket No. PP0052).
• the film layers used herein may be metal (such as aluminum foil) or polymeric.
• Suitable polymeric film materials include, but are not limited to, those described in U.S. Provisional Appln. No. 61/141 ,836, cited above.
• abrasion resistant hardcoat Any material known for use in abrasion resistant hardcoats may be used herein. Suitable materials include, but are not limited to, those described in U.S. Provisional Appln. No. 61/141 ,836, cited above.
• the safety laminates may further comprise other polymeric interlayer sheets formed of polymeric materials, such as polyvinyl acetal) (e.g., polyvinyl butyral) (PVB)), polyvinyl chloride), polyurethane, ethylene/vinyl acetate copolymers, acid copolymers, other ionomers, or combinations of two or more thereof.
• polymeric interlayer sheets may be formed of polymeric materials that are the same or different.
• Each of the interlayer sheets comprising the ethylene copolymer or ionomer compositions and each of the other polymeric interlayer sheets comprised in the safety laminates may have a thickness of at least about 5 mils (0.1 mm), or at least about 30 mils (0.8 mm), or about 30 to about 200 mils (about 0.8 to about 5.1 mm), or about 45 to about 200 mils (about 1 .1 to about 5.1 mm), or about 45 to about 100 mils (about 1.1 to about 2.5 mm), or about 45 to about 90 mils (about 1 .1 to about 2.3 mm).
• the inner sub-layer comprising the ethylene copolymer composition may have a thickness ranging from about 10 to about 30 mils (about 0.25 to about 0.76 mm) while the surface sub-layer comprising the ethylene copolymer composition may have a thickness of about 1 to about 5 mils (about 0.025 to about 0.12 mm).
• One preferred safety laminate comprises (a) a first rigid sheet or film layer, which is laminated to (b) a sheet comprising the ethylene copolymer or ionomer composition, which is laminated to (c) a second rigid sheet or film layer.
• the safety laminate may comprise two glass sheets with an interlayer sheet laminated between the two glass sheets, or the safety laminate may comprise a glass sheet and a hardcoated polyester film with an interlayer sheet comprising the ethylene copolymer or sodium ionomer composition laminated between the glass sheet and the hardcoated plastic film.
• Another safety laminate may comprise n plies of rigid sheet or film layers (such as glass sheet layers) and n-1 plies of polymer interlayer sheets, wherein (a) each adjacent pair of the rigid sheet or film layers are interspaced by one of the polymer interlayer sheets; (b) at least one, or preferably each, of the polymer interlayer sheets is the sodium ionomer interlayer sheet disclosed above, and (c) n is an integer and 2 ⁇ n ⁇ 10.
• Such safety laminates are described at length in U.S. Patent Appln. No. 12/215,839, filed on June 30, 2008.
• the safety laminates disclosed here may take any form known within the art. Some specific constructions include, but are not limited to, those set forth in U.S. Patent Appln. Publn. No. 2010/01 1235 (Attorney Docket No. PP0036). Some examples of preferred safety laminates include, but are not limited to, rigid sheet/interlayer sheet; polymer film/interlayer sheet; rigid sheet/interlayer sheet/polymer film; rigid sheet/interlayer sheet/rigid sheet;
• one or both surfaces of any of the component layers comprised in the safety laminate may be treated prior to the lamination process to enhance the adhesion to other laminate layers.
• This adhesion enhancing treatment may take any form known within the art and includes flame treatments (see, e.g., U.S. Patent Nos. 2,632,921 ; 2,648,097; 2,683,894; and 2,704,382), plasma treatments (see e.g., U.S. Patent No. 4,732,814), electron beam treatments, oxidation treatments, corona discharge treatments, chemical treatments, chromic acid treatments, hot air treatments, ozone treatments, ultraviolet light treatments, sand blast treatments, solvent treatments, and combinations of two or more thereof.
• the adhesion strength may be further improved by further applying an adhesive or primer coating on the surface of the laminate layer(s).
• U.S. Patent No. 4,865,71 1 discloses a film or sheet with improved bondability, which has a thin layer of carbon deposited on one or both surfaces.
• suitable adhesives or primers include silanes, poly(allyl amine) based primers (see, e.g., U.S. Patent Nos. 5,41 1 ,845; 5,770,312; 5,690,994; and 5,698,329), and acrylic based primers (see, e.g., U.S. Patent No.
• the adhesive or primer coating may take the form of a monolayer of the adhesive or primer and have a thickness of about 0.0004 to about 1 mil (about 0.00001 to about 0.03 mm), or preferably, about 0.004 to about 0.5 mil (about 0.0001 to about 0.013 mm), or more preferably, about 0.004 to about 0.1 mil (about 0.0001 to about 0.003 mm).
• any lamination process known within the art may be used to prepare the safety laminates.
• the laminate may be made by an autoclave process, such as disclosed in U.S. Patent No. 3,31 1 ,517, or a non-autoclave lamination process, such as disclosed in U.S. Patent Nos. 3,234,062; 3,852,136; 4,341 ,576; 4,385,951 ; 4,398,979; 5,536,347; 5,853,516; 6,342,1 16; and 5,415,909, U.S. Patent Publication No. 2004/0182493, European Patent No. EP 1 235 683 B1 , PCT Patent Publication Nos.
• the temperature and duration of the lamination are such that the ethylene copolymer composition becomes at least partially cross-linked. More specifically, it may be necessary to maintain the temperature of the laminate at 10 to 30°C, 10 to 40°C, 10 to 50°C, 10 to 60°C, 10 to 70°C, 10 to 80°C, 10 to 90°C, or 10 to 100°C higher than the softening temperature of the second film layer for a period of one to 10 minutes, or one to 30 minutes, or one to 60 minutes, to achieve adhesion and cross-linking, if desired.
• Ethylene Copolymer 1 is an ionomer rather than an ethylene acid copolymer.
• the following examples are provided to describe the invention in further detail. These examples, which set forth a preferred mode presently contemplated for carrying out the invention, are intended to illustrate and not to limit the invention.
• melt indices (Ml) and melt flow rates (MFR) reported herein were determined in accordance with ASTM D1238 at 190°C and 2.16 kg, and are reported in units of g/10 min, unless otherwise specified in limited circumstances.
• ACR-1 a terpolymer containing 66.9 weight % copolymerized ethylene units, 23.5 weight % copolymerized n-butyl acrylate units and 9.6 weight % copolymerized methacrylic acid units, MFR 25 g/10 minutes at 190°C, 2.16 kg as measured in accordance with ASTM D 1238.
• EBAGMA-1 a terpolymer containing 66.75 weight % copolymerized ethylene units, 28 weight % copolymerized n-butyl acrylate units and 5.25 weight % copolymerized glycidyl methacrylate units, MFR 12 g/ 10 minutes at 190°C, 2.16 kg as measured in accordance with ASTM D 1238.
• EBAGMA-2 a terpolymer containing 64 weight % copolymerized ethylene units, 25 weight % copolymerized n-butyl acrylate units and 9 weight % copolymerized glycidyl methacrylate units, MFR 8 g/10 minutes at190°C, 2.16 kg as measured in accordance with ASTM D 1238.
• EBA-1 an ethylene/n-butyl acrylate dipolymer containing 73 weight % copolymerized ethylene units and 27 weight % copolymerized n-butyl acrylate units, MFR 4 g/10 minutes at 190°C, 2.16 kg, measured according to ASTM D 1238.
• EMAME-1 an ethylene/ethyl hydrogen maleate dipolymer containing 91.5 weight% copolymerized ethylene units and 9.5 weight % copolymerized ethyl hydrogen maleate units, MFR 25 g/10 minutes at 190°C. 2.16 kg measured in accordance with ASTM D 1238.
• ION-2 An ethylene/methacrylic acid copolymer containing 85 weight % copolymerized ethylene units and 15 weight % copolymerized methacrylic acid units 23 % nominally neutralized to Zn salts, melt flow rate 5.5 g/10 minutes at 190°C, 2.16 kg, measured in accordance with ASTM D 1238.
• APTMS 3-aminopropyltrimethoxysilane, available from Sigma-Aldrich Co., catalog number 28, 177-8
• MAOTMS methacryloyloxypropyltrimethoxysilane, available from Sigma-Aldrich Co.
• Bixcure® A commercial EVA encapsulant sheet comprising an ethylene/vinyl acetate dipolymer blended with a proprietary modifier package including a crosslinking agent, an adhesion promoter, and various stabilizers available from Bixby International Corporation, One Preble Road, Newburyport, MA USA 01950. The sheet was stored in a freezer as received until it was used in the laminations. Experimental Method and Results
• Formulations were prepared from the components listed in Table 1 , where the amount of each component in the composition is listed in "parts”.
• the components of Comparative Example C3 were melt blended in an extruder and collected as pellets.
• compositions that included the silane coupling agents APTMS or MAOTMS were prepared by mixing polymer pellets with the liquid silane additives and permitting the pellets to imbibe the additives.
• the modified pellets were fed to a twin screw extruder for preparing extruded polymer sheet compositions.
• Sheets of the compositions were then formed by extrusion casting or press molding.
• the polymer pellets were fed to a single screw or twin screw extruder, melted, conveyed, and forced through a suitably shaped (e.g., linear slot) die to produce the desired cross-sectional sheet shape.
• a suitably shaped die e.g., linear slot
• the polymeric sheets were cast onto a water-cooled chilled roll for solidification, collected by winding on cardboard cores and stored for later laminations.
• Table 1 summarizes the extrusion casting conditions. In Table 1 , "TS" indicates twin screw extruder and "SS" indicates single screw extruder.
• the first ethylene copolymer had a melt flow rate (MFR) of 300 g/10 min and comprised copolymerized units of ethylene (65.8 wt%), n-butyl acrylate (28 wt%), and acrylic acid (6.2 wt%).
• the second ethylene copolymer had a MFR of 8 g/10 min and comprised
• the weight ratio of the first ethylene copolymer to the second ethylene copolymer was 60 to 40.
• the molar ratio between the acid group in the first ethylene copolymer and the glycidyl group in the second ethylene copolymer was 2.04 to 1.
• the MFR of the blend of the two ethylene copolymers remained at above 200 g/10 min. (All MFR reported herein were determined in accordance with ASTM D1238 at 190°C and 2.16 kg, and are reported in units of g/10 min, unless otherwise specified in limited
• a plaque having a thickness of 30 mil was formed by compression molding a portion of the blend at 160°C for 15 minutes.
• the measurement of the MFR of the plaque was attempted, only a hard gel formed in the melt indexer. It was therefore concluded that the polymer blend in the plaque was cross-linked.
• the plaque was clear, with a total transmission value of 92%, as measured with a HunterLab Color Quest XE
• the plaque also had a tensile modulus of 886 psi, as measured by ASTM D1708 at ambient temperature on 19 mil thick microtensile bars using an Instru-Met (Model 1 122) and a test speed of 2 in/min.
• the first ethylene copolymer had a melt flow rate (MFR) of 210 g/10 min and comprised copolymerized units of ethylene (65.8 wt%), n-butyl acrylate (28 wt%), and acrylic acid (6.2 wt%).
• the second ethylene copolymer had a MFR of 12 g/10 min and comprised
• the weight ratio of the first ethylene copolymer to the second ethylene copolymer was 60 to 40.
• the molar ratio between the acid group in the first ethylene copolymer and the glycidyl group in the second ethylene copolymer was 3.5 to 1.
• the MFR of the blend of the two ethylene copolymers was 70 g/10 min.
• the first ethylene copolymer had a melt flow rate (MFR) of 60 g/10 min and comprised copolymerized units of ethylene (65.8 wt%), n-butyl acrylate (28 wt%), and acrylic acid (6.2 wt%).
• the second ethylene copolymer had a MFR of 12 g/10 min and comprised
• the weight ratio of the first ethylene copolymer to the second ethylene copolymer was 60 to 40.
• the molar ratio between the acid group in the first ethylene copolymer and the glycidyl group in the second ethylene copolymer was 3.5 to 1 .
• the MFR of the blend of the two ethylene copolymers was 25 g/10 min.
• a clear plaque having a thickness of 125 mil was formed by compression molding a portion of the blend at 175°C for 15 minutes.
• MFR of the clear plaque was measured by compression molding a portion of the blend at 175°C for 15 minutes.
• the first ethylene copolymer had a melt flow rate (MFR) of 210 g/10 min and comprised copolymerized units of ethylene (65.8 wt%), n-butyl acrylate (28 wt%), and acrylic acid (6.2 wt%).
• the second ethylene copolymer had a MFR of 8 g/10 min and comprised
• the weight ratio of the first ethylene copolymer to the second ethylene copolymer was 60 to 40.
• the molar ratio between the acid group in the first ethylene copolymer and the glycidyl group in the second ethylene copolymer was 2.04 to 1.
• the MFR of the blend of the two ethylene copolymers was 57 g/10 min.
• the first ethylene copolymer had a melt index (Ml) of 12, and comprised copolymerized units of ethylene (66.75 wt%), n-butyl acrylate (28 wt%), and glycidyl methacrylate (5.25 wt%).
• the second ethylene copolymer had a Ml of 60 and comprised copolymerized units of ethylene (66.0 wt%), n-butyl acrylate (28 wt%), and acrylic acid (6 wt%).
• the blend was 59.5 wt% of the first ethylene copolymer, 40 wt% of the second ethylene copolymer, and 0.5 wt% of the silane (gamma- glycidoxypropyltrimethyoxysilane).
• the Ml of the blend was 20 (measured at 125 °C and extrapolated to 190 °C).
• the melt flow (in a 10 minute period) was measured in a melt indexer with a 2160 gram weight at several different temperatures after being held at the specific temperature in the melt indexer for 10 minutes. The results are set forth in Table 2 below:
• a plaque (20 mil thickness) of the uncrosslinked blend was prepared by compression molding at 120 °C and holding at that temperature for 2 minutes. Based on the results set forth above, no crosslinking occurs under these conditions.
• a pre-press assembly was laid up by stacking, in the order given, the following layers: glass/Teflon® 500A FEP 100/TPT [Tedlar®/PET/Tedlar®]/ Encapsulant/Teflon® 500A FEP 100 slip sheet/glass.
• the encapsulant was the 20 mil plaque of the
• Teflon® slip sheet whose dimensions were 1.5 inches by 4 inches.
• the glass was used as received from St. Gobain (Diamant solar glass).
• the Teflon® FEP 500A was used as received from DuPont.
• the TPT Tedlar®/Poly(ethylene) terephthalate/ Tedlar®
• the Teflon® film slip sheet was placed between the
• perfluorinated copolymer resin film and the sample film at one end of the overlay to provide an unlaminated (unadhered) region to serve as an initiation point for subsequent peel tests.
• the pre-press assembly was placed in a vacuum bag and was vacuum laminated using a VWR Programmable Oven, Model No. 1685. To begin the heating cycle, the structure was heated from ambient temperature (-25 °C) to 140 °C in 15 minutes and then held at that temperature for 5 minutes. Then it was heated to 170 °C and held for 10 minutes. The encapsulant blend was completely crosslinked under these conditions, as shown by the data in Table 2, above.
• peel strength 180 degree peel at 10 inches/min
• the peel strength (180 degree peel at 10 inches/min) of the encapsulant to glass was measured both before and after being exposed to damp heat (85 °C, 85% relative humidity) in a damp heat chamber (Tenny Product Solutions, Model No. BTRC) for 1 180 hours. Peel strength was determined to be 78 psi before exposure and 91 psi after exposure as measured on an Instru-Met adhesion tester, Model No. 1 122.
• the percent transmittance of the structure was measured at three different wavelengths on a Hunter Lab Color Quest XE spectrophotometer, with the following results in Table 3 below:
• the Ml of the blend was 15 (measured at 125 °C and extrapolated to 190 °C).
• the flow of the blend was measured in a melt indexer in a 10 minute period with a 2160 gram weight at several different temperatures, after being held at the specific temperature in the melt indexer for 10 minutes. The results are set forth in Table 4 below: Table 4
• a second blend of the first and the second ethylene copolymer was made.
• the second blend was similar to the blend described above and made under similar conditions, but did not include the 4-dimethylamino-pyridine.
• the melt flow of the second blend was measured by the procedure described above, the following results were obtained, as shown in Table 5:
• the blend composition was 20 wt% zinc ionomer and 80 wt% ethylene copolymer.
• the melt index (Ml) of the blend was 4, when measured at 125°C and extrapolated to 190°C. Flow in a 10 minute period in a melt indexer with a 2160 gram weight was determined at several different temperatures after being held at the specific temperature in the melt indexer for 10 minutes. The results are shown in Table 9 below. Table 9

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