WO2006113000B1 - Cap liners, closures and gaskets from multi-block polymers - Google Patents

Cap liners, closures and gaskets from multi-block polymers

Info

Publication number
WO2006113000B1
WO2006113000B1 PCT/US2006/009501 US2006009501W WO2006113000B1 WO 2006113000 B1 WO2006113000 B1 WO 2006113000B1 US 2006009501 W US2006009501 W US 2006009501W WO 2006113000 B1 WO2006113000 B1 WO 2006113000B1
Authority
WO
WIPO (PCT)
Prior art keywords
ethylene
percent
interpolymer
gasket
polymer
Prior art date
Application number
PCT/US2006/009501
Other languages
French (fr)
Other versions
WO2006113000A2 (en
WO2006113000A3 (en
Inventor
Ronald Paul Markovich
Dale M Elley-Bristow
Miguel Alberto Prieto
Russell Paul Barry
Felipe Martinez
Daniel J Falla
Julien H J M Damen
Original Assignee
Dow Global Technologies Inc
Ronald Paul Markovich
Dale M Elley-Bristow
Miguel Alberto Prieto
Russell Paul Barry
Felipe Martinez
Daniel J Falla
Julien H J M Damen
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/US2005/008917 external-priority patent/WO2005090427A2/en
Priority to CN2006800083690A priority Critical patent/CN101426880B/en
Priority to JP2008502036A priority patent/JP5227786B2/en
Priority to BRPI0609824-0A priority patent/BRPI0609824B1/en
Priority to CA002601263A priority patent/CA2601263A1/en
Priority to MX2007011334A priority patent/MX2007011334A/en
Application filed by Dow Global Technologies Inc, Ronald Paul Markovich, Dale M Elley-Bristow, Miguel Alberto Prieto, Russell Paul Barry, Felipe Martinez, Daniel J Falla, Julien H J M Damen filed Critical Dow Global Technologies Inc
Priority to US11/908,951 priority patent/US7592397B2/en
Priority to EP06769781.3A priority patent/EP1877513B1/en
Priority to AU2006237514A priority patent/AU2006237514B2/en
Publication of WO2006113000A2 publication Critical patent/WO2006113000A2/en
Publication of WO2006113000A3 publication Critical patent/WO2006113000A3/en
Publication of WO2006113000B1 publication Critical patent/WO2006113000B1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D53/00Sealing or packing elements; Sealings formed by liquid or plastics material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F10/14Monomers containing five or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F295/00Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/02Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
    • C08F297/04Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/06Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
    • C08F297/08Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/06Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
    • C08F297/08Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
    • C08F297/083Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/06Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
    • C08F297/08Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
    • C08F297/083Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
    • C08F297/086Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene the block polymer contains at least three blocks
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0807Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
    • C08L23/0815Copolymers of ethene with aliphatic 1-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/005Modified block copolymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • C08L53/025Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes modified
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/10Materials in mouldable or extrudable form for sealing or packing joints or covers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F110/00Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F110/02Ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2410/00Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
    • C08F2410/01Additive used together with the catalyst, excluding compounds containing Al or B
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62Refractory metals or compounds thereof
    • C08F4/64Titanium, zirconium, hafnium or compounds thereof
    • C08F4/659Component covered by group C08F4/64 containing a transition metal-carbon bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62Refractory metals or compounds thereof
    • C08F4/64Titanium, zirconium, hafnium or compounds thereof
    • C08F4/659Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65908Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62Refractory metals or compounds thereof
    • C08F4/64Titanium, zirconium, hafnium or compounds thereof
    • C08F4/659Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65912Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/16Ethene-propene or ethene-propene-diene copolymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0869Acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0869Acids or derivatives thereof
    • C08L23/0876Neutralised polymers, i.e. ionomers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2200/00Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K2200/06Macromolecular organic compounds, e.g. prepolymers
    • C09K2200/0615Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09K2200/0617Polyalkenes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2200/00Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K2200/06Macromolecular organic compounds, e.g. prepolymers
    • C09K2200/0615Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09K2200/0617Polyalkenes
    • C09K2200/062Polyethylene

Abstract

A polymer composition comprises at least an ethylene/α-oleiln interpolymer and at least one other polymer. The other polymer can be selected from a second ethylene/α-olefm interpolymer, an elastomer, a polyolefin, a polar polymer, and an ethylene/carboxylic acid interpolymer or ionomer thereof. The ethylene/α-olefm interpolymer is a block copolymer having at least a hard block and at least a soft block. The soft block comprises a higher amount of comonomers than the hard block. The block interpolymer has a number of unique characteristics disclosed here. Also provided are gaskets, bottle cap liners, and closures that comprise or obtained from a compositon comprising at least one ethylene/α-olefm interpolymer and at least one polyolefin. The gaskets are capable of compression sealing various containers, without contaminating the contents. Liquid containers particularly benefit from the use of the novel gasket materials disclosed herein.

Claims

AMENDED CLAIMS received by the International Bureau on 30 August 2007 (30.08.2007)What is claimed is:
1. A gasket comprising or obtainable from a composition comprising: (A) about 80 to about 97.5 weight percent, based on the total weight of components (A), (B) and (C), of at least one ethylene/α-olefin interpolymer; wherein the ethylene/α-olefϊn interpolymer is a block interpolymer and:
(a) has a Mw/Mn from about 1.7 to about 3.5, at least one melting point, Tm, in degrees Celsius, and a density, d, in grams/cubic centimeter, wherein the numerical values of Tm and d correspond to the relationship:
Tm > -2002.9 + 4538.5(d) - 2422.2(d)2, or (b) has a Mw/Mn from about 1.7 to about 3.5, and is characterized by a heat of fusion, ΔH in J/g, and a delta quantity, ΔT, in degrees Celsius, defined as the temperature difference between the tallest DSC peak and the tallest CRYSTAF peak, wherein the numerical values of ΔT and ΔH have the following relationships:
ΔT > -0.1299(ΔH) + 62.81 for ΔH greater than zero and up to 130 J/g, ΔT > 480C for ΔH greater than 130 J/g , wherein the CRYSTAF peak is determined using at least 5 percent of the cumulative polymer, and if less than 5 percent of the polymer has an identifiable CRYSTAF peak, then the CRYSTAF temperature is 3O0C; or
(c) is characterized by an elastic recovery, Re, in percent at 300 percent strain and 1 cycle measured with a compression-molded film of the ethylene/α- olefin interpolymer, and has a density, d, in grams/cubic centimeter, wherein the numerical values of Re and d satisfy the following relationship when ethylene/α-olefin interpolymer is substantially free of a cross-linked phase:
Re >1481-1629(d); or (d) has a molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a molar comonomer content of at least 5 percent higher than that of a comparable random ethylene interpolymer fraction eluting between the same temperatures, wherein said comparable random ethylene interpolymer has the same comonomer(s) and has a melt index, density, and molar comonomer content (based on the whole polymer) within 10 percent of that of the ethylene/α-olefin interpolymer; or 119
(e) has a storage modulus at 250C, G' (250C), and a storage modulus at 1000C, G'(100°C), wherein the ratio of G'(25°C) to G'(100°C) is in the range of about 1:1 to about 9:1;
(B) about 2 to about 15 weight percent of at least one ethylene/carboxylic acid interpolymer or an ionomer thereof based on the total weight of components (A), (B) and (C); and
(C) at least one slip agent.
2. The gasket of claim 1, wherein the ethylene interpolymer of (A) comprises an ethylene/C3-C20 alpha-olefin interpolymer.
3. The gasket of claim 2 wherein the ethylene interpolymer of (A) has:
(i) a density from about 0.85 g/cm3 to about 0.96 g/cm3, (ii) a molecular weight distribution from about 1.8 to about 2.8, (iii) a melt index from about 0.15 g/10 minutes to about 100 g/10 minutes, and (iv) a single melting peak as measured using differential scanning calorimetry.
4. The gasket of claim 1 or 3, wherein the ethylene interpolymer of (A) is further blended with a heterogeneously branched ethylene polymer.
5. The gasket of claim 1 or 3, wherein the ethylene interpolymer of (A) is further blended a heterogeneously branched ethylene interpolymer having:
(i) a density from about 0.86 g/cm3 to about 0.92 g/cm3, and (ii) a melt index from about 0.15 g/10 minutes to about 100 g 10 minutes.
6. The gasket of claim 1 or 3, wherein the ethylene interpolymer comprises from about 85 percent by weight of total composition to about 97.5 percent by weight based on the total weight of the components (A), (B), and (C).
7. The gasket of claim 1 or 3, wherein the ethylene/carboxylic acid interpolymer or ionomer thereof comprises from about 4 percent by weight of total composition to about
12 percent by weight based on the total weight of the components (A), (B), and (C).
8. The gasket of claim 1 or 3, wherein the ethylene/carboxylic acid interpolymer has an acid content from about 3 percent by weight of the interpolymer to about 50 percent by weight of the interpolymer.
9. The gasket of claim 1 or 3, wherein the ethylene/carboxylic acid interpolymer has a melt index from about 0.15 g/10 minutes to about 400 g/10 minutes.
10. The gasket of claim 1 or 3, wherein the slip agent comprises from about 0.05 percent by weight of the total composition to about 5 percent by weight of the total 120
composition.
11. The gasket of claim 1 or 3, wherein the slip agent comprises a primary amide agent and a secondary amide agent, together comprising from about 0.05 percent by weight of the total composition to about 5 percent by weight of the total composition.
12. The gasket of claim 11 , wherein the primary amide agent is present at a level at least twice that of the secondary amide agent.
13. The gasket according to claim 1 or 3, wherein components (A), (B), and (C) of claim 1 together comprise from about 80 percent by weight of the gasket to 100 percent by weight of the gasket.
14. The gasket of claim 1 or 3, wherein the gasket is a foamed gasket.
15. The foamed gasket of claim 14, wherein the foaming agent is selected from the group consisting of physical blowing agents, gaseous blowing agents and chemical blowing agents.
16. The foamed gasket of claim 14, wherein the foaming agent is a chemical blowing agent selected from the group consisting of sodium bicarbonate, dinitrosopentamethylenetetramine, sulfonyl hydrazides, azodicarbonamide, p-toluenesulfonyl semicarbazide, 5-phenyltetrazole, diisopropylhydrazodicarboxylate, 5-phenyl-3,6-dihydro- l,3,4-oxadiazin-2-one, and sodium borohydride.
17. The foamed gasket of claim 14, wherein the foaming agent is a gaseous blowing agent selected from the group consisting of carbon dioxide and nitrogen.
18. The foamed gasket of claim 14, wherein the foaming agent is a physical blowing agent selected from the group consisting of pentanes, hexanes, heptanes, benzene, toluene, dichloromethane, trichloromethane, trichloroethylene, tetrachloromethane, 1,2- dichloroethane, trichlorofluoromethane, 1,1,2-trichlorotrifluoroethane, methanol, ethanol, 2- propanol, ethyl ether, isopropyl ether, acetone, methyl ethyl ketone, and methylene chloride; isobutane and n-butane, 1,1-difluoroethane.
19. The gasket of claim 3, wherein the ethylene/carboxylic acid interpolymer has an acid content from about 3 percent by weight of the interpolymer to about 50 percent by weight of the interpolymer and a melt index from about 0.15 g/10 min. to about 400 g/10 minutes, and the slip agent (C) comprises a primary amide agent and a secondary amide agent, the primary and secondary amide agents together comprising from about 0.05 percent by weight of the total composition to about 5 percent by weight of the total composition. 121
20. The gasket of claim 19, wherein the primary amide agent is present at a level at least twice that of the secondary amide agent.
21. A process for preparing a synthetic cork closure for a liquid container having at least a portion thereof coated with a gas impermeable polymer which comprises providing a synthetic cork closure and coating at least a portion thereof with a gas impermeable polymer, wherein the synthetic closure comprises a composition comprising:
(A) about 80 to about 97.5 weight percent, based on the total weight of components (A), (B) and (C), of at least one ethylene/α-olefin interpolymer; wherein the ethylene/α-olefin interpolymer is a block interpolymer and: (a) has a Mw/Mn from about 1.7 to about 3.5, at least one melting point, Tm, in degrees Celsius, and a density, d, in grams/cubic centimeter, wherein the numerical values of Tm and d correspond to the relationship:
Tm > -2002.9 + 4538.5(d) - 2422.2(d)2, or
(b) has a Mw/Mn from about 1.7 to about 3.5, and is characterized by a heat of fusion, ΔH in J/g, and a delta quantity, ΔT, in degrees Celsiuss defined as the temperature difference between the tallest DSC peak and the tallest CRYSTAF peak, wherein the numerical values of ΔT and ΔH have the following relationships:
ΔT > -0.1299(ΔH) + 62.81 for ΔH greater than zero and up to 130 J/g, ΔT > 48°C for ΔH greater than 130 J/g , wherein the CRYSTAF peak is determined using at least 5 percent of the cumulative polymer, and if less than 5 percent of the polymer has an identifiable CRYSTAF peak, then the CRYSTAF temperature is 300C; or
(c) is characterized by an elastic recovery, Re, in percent at 300 percent strain and 1 cycle measured with a compression-molded film of the ethylene/α- olefin interpolymer, and has a density, d, in grams/cubic centimeter, wherein the numerical values of Re and d satisfy the following relationship when ethylene/α-olefin interpolymer is substantially free of a cross-linked phase:
Re >1481-1629(d); or
(d) has a molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a molar comonomer content of at least 5 percent higher than that of a comparable random 122 ethylene interpolymer fraction eluting between the same temperatures, wherein said comparable random ethylene interpolymer has the same comonomer(s) and has a melt index, density, and molar comonomer content (based on the whole polymer) within 10 percent of that of the ethylene/α-olefin interpolymer; or (e) has a storage modulus at 25°C, G' (250C), and a storage modulus at 1000C, G'(100°C), wherein the ratio of G'(25°C) to G'(100°C) is in the range of about 1 : 1 to about 9:1.
(B) about 2 to about 15 weight percent of at least one ethylene/carboxylic acid interpolymer or an ionomer thereof based on the total weight of components (A), (B) and (C); and
(C) at least one slip agent.
22. The process of claim 21 wherein the gas impermeable polymer is a vinylidene chloride polymer.
23. The process of claim 22, wherein the gas impermeable polymer is a vinylidene chloride polymer, which is (1) a copolymer of (a) from about 80 to about 93 mole percent vinylidene chloride and (b) from about 20 to about 7 mole percent of at least one monoethylenically unsaturated monomer copolymerizable therewith or (2) a copolymer of (a) from about 65 to about 75 mole percent vinylidene chloride and (b) from about 35 to about 25 mole percent of at least one monoethylenically unsaturated monomer copolymerizable therewith.
24. A polymer blend composition comprising:
(A) at least one ethylene/α-olefin interpolymer and (B) at least one other polymer, wherein the ethylene/α-olefin interpolymer is a block interpolymer and:
(a) has a Mw/Mn from about 1.7 to about 3.5, at least one melting point, Tm, in degrees Celsius, and a density, d, in grams/cubic centimeter, wherein the numerical values of Tm and d correspond to the relationship:
Tm > -2002.9 + 4538.5(d) - 2422.2(d)2, or
(b) has a Mw/Mn from about 1.7 to about 3.5, and is characterized by a heat of fusion, ΔH in J/g, and a delta quantity, ΔT, in degrees Celsius^ defined as the temperature difference between the tallest DSC peak and the tallest CRYSTAF peak, wherein the numerical values of ΔT and ΔH have the following relationships:
ΔT > -0.1299(ΔH) + 62.81 for ΔH greater than zero and up to 130 J/g, 123
ΔT > 480C for ΔH greater than 130 J/g , wherein the CRYSTAF peak is determined using at least 5 percent of the cumulative polymer, and if less than 5 percent of the polymer has an identifiable CRYSTAP peak, then the CRYSTAF temperature is 3O0C; or (c) is characterized by an elastic recovery, Re, in percent at 300 percent strain and 1 cycle measured with a compression-molded film of the ethylene/α- olefin interpolymer, and has a density, d, in grams/cubic centimeter, wherein the numerical values of Re and d satisfy the following relationship when ethylene/α-olefin interpolymer is substantially free of a cross-linked phase: Re >1481-1629(d); or
(d) has a molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a molar comonomer content of at least 5 percent higher than that of a comparable random ethylene interpolymer fraction eluting between the same temperatures, wherein said comparable random ethylene interpolymer has the same comonomer(s) and has a melt index, density, and molar comonomer content (based on the whole polymer) within 10 percent of that of the ethylene/α-olefin interpolymer; or
(e) has a storage modulus at 250C, G' (250C), and a storage modulus at 1000C, G'(100°C), wherein the ratio of G'(25°C) to G'(100°C) is in the range of about 1 : 1 to about 9: 1 ; or
(f) at least one molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a block index of at least 0.5 and up to about 1 and a molecular weight distribution, Mw/Mn, greater than about 1.3; or
(g) an average block index greater than zero and up to about 1.0 and a molecular weight distribution, Mw/Mn, greater than about 1.3.
25. The composition of claim 24, wherein the other polymer is selected from a second ethylene/α-olefin interpolymer, an elastomer, a polyolefin, a polar polymer, and an ethylene/carboxylic acid interpolymer or ionomer thereof, the second ethylene/α-olefm interpolymer is different that the first ethylene/α-olefin interpolymer and the second ethylene/α-olefin interpolymer: 124
(a) has a Mw/Mn from about 1.7 to about 3.5, at least one melting point, Tm, in degrees Celsius, and a density, d, in grams/cubic centimeter, wherein the numerical values of Tm and d correspond to the relationship:
Tm > -2002.9 + 4538.5(d) - 2422.2(d)2, or (b) has a Mw/Mn from about 1.7 to about 3.5, and is characterized by a heat of fusion, ΔH in J/g, and a delta quantity, ΔT, in degrees Celsius., defined as the temperature difference between the tallest DSC peak and the tallest CRYSTAF peak, wherein the numerical values of ΔT and ΔH have the following relationships:
ΔT > -0.1299(ΔH) + 62.81 for ΔH greater than zero and up to 130 J/g, ΔT > 480C for ΔH greater than 130 J/g , wherein the CRYSTAF peak is determined using at least 5 percent of the cumulative polymer, and if less than 5 percent of the polymer has an identifiable CRYSTAF peak, then the CRYSTAF temperature is 3O0C; or
(c) is characterized by an elastic recovery, Re, in percent at 300 percent strain and 1 cycle measured with a compression-molded film of the ethylene/α- olefin interpolymer, and has a density, d, in grams/cubic centimeter, wherein the numerical values of Re and d satisfy the following relationship when ethylene/α-olefin interpolymer is substantially free of a cross-linked phase:
Re >1481-1629(d); or (d) has a molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a molar comonomer content of at least 5 percent higher than that of a comparable random ethylene interpolymer fraction eluting between the same temperatures, wherein said comparable random ethylene interpolymer has the same comonomer(s) and has a melt index, density, and molar comonomer content (based on the whole polymer) within 10 percent of that of the ethylene/α-olefϊn interpolymer; or
(e) has a storage modulus at 250C, G' (250C), and a storage modulus at 1000C, G'(100°C), wherein the ratio of G'(25°C) to G'(100°C) is in the range of about 1:1 to about 9:1; or 125
(f) at least one molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a block index of at least 0.5 and up to about 1 and a molecular weight distribution, Mw/Mn, greater than about 1.3; or
(g) an average block index greater than zero and up to about 1.0 and a molecular weight distribution, Mw/Mn, greater than about 1.3.
26. The composition of claim 24 or 25, wherein the first ethylene/α-olefin interpolymer is present in an amount ranging from about 9% to 99.5% and the second ethylene/α-olefin interpolymer is present in an amount ranging from about 9% to 99.5% by weight of the total weight of the composition.
27. The composition of claim 24 or 25, wherein the other polymer is an elastomer selected from a thermoplastic vulcanizate, styrenic block copolymer, neoprene, functionalized elastomers, polybutadiene rubber, butyl rubber or a combination thereof.
28. The composition of claim 24 or 25, wherein the other polymer is a polyolefin selected from LDPE, LLDPE, HDPE, EVA, EAA, EMA, ionomers thereof, metallocene LLDPE, impact grade propylene polymer, random grade propylene polymer, polypropylene and a combination thereof.
29. The composition of claim 24 or 25, wherein the other polymer is a polar polymer selected from nylon, polyamide, ethylene vinyl acetate, polyvinyl chloride, acrylonitrile/butadiene/styrene (ABS) copolymers, aromatic polycarbonate, ethylene / carboxylic acid copolymers, polyacrylic and a combination thereof.
30. The composition of claim 24 or 25, wherein the other polymer is an olefin/carboxylic acid interpolymer selected from ethylene-acrylic acid copolymer, ethylene- methacrylic acid copolymer, ethylene-itaconic acid copolymer, ethylene-methyl hydrogen maleate copolymer, ethylene-maleic acid copolymer, ethylene-acrylic acid copolymer, ethylene-methacrylate copolymer, ethylene-methacrylic acid-ethacrylate copolymer, ethylene-itaconic acid- methacrylate copolymer, ethylene-itaconic acid-methacrylate copolymer, ethylene-methyl hydrogen maleate-ethyl acrylate copolymer, ethylene- methacrylic acid-vinyl acetate copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic acid- vinyl alcohol copolymer, ethylene-acrylic acid-carbon monoxide copolymer, ethylene- propylene-acrylic acid copolymer, ethylene-methacrylic acid-acrylonitrile copolymer, ethylene-fumaric acid- vinyl methyl ether copolymer, ethylene- vinyl chloride-acrylic acid copolymer, ethylene-vinylidene chloride-acrylic acid copolymer, ethylene-vinylidene 126
chloride-acrylic acid copolymer,ethylene-vinyl fluoride-methacrylic acid copolymes, ethylene-chlorotrifluoroethlyene-methacrylic acid copolymer, or a combination thereof.
31. The composition of claim 24 or 25, further comprising an additive selected from a slip agent, an anti-blocking agent, a plasticizer, an antioxidant, a UV stabilizer, a colorant, a filler, a lubricant, an antifogging agent, a flow aid, a acoupling agent, a cross- linking agent, a nucleating agent, a surfactant, a solvent, a flame retardant, an antistatic agent, an extender, an odor absorber, a barrier resin and a combination thereof.
32. The composition of claim 31, wherein the slip agent is polymethylsiloxane, erucamide, oleamide or a combination thereof.
33. The composition of claim 31 , wherein the odor absorber is calcium carbonate, activated charcoal or a combination thereof.
34. The composition of claim 31 , wherein the barrier resin is ethylene vinyl alcohol (EVOH) copolymer or polyvinylidene chloride (PVDC).
35. The composition of claim 31, wherein the extender is a mineral oil, polybutene, siloxane, or a combination thereof.
36. A gasket comprising the composition of any of claims 24-35.
37. The gasket of claim 36, wherein the ethylene/carboxylic acid interpolymer or ionomer thereof comprises from about 4 percent to about 12 percent by weight of total composition.
38. The gasket of claim 37, wherein the ethylene/carboxylic acid interpolymer has an acid content from about 3 percent by weight of the interpolymer to about 50 percent by weight of the interpolymer.
39. The gasket of claim 36, wherein the slip agent comprises a primary amide agent and a secondary amide agent, together comprising from about 0.05 percent by weight of the total composition to about 5 percent by weight of the total composition.
40. The gasket of claim 39, wherein the primary amide agent is present at a level at least twice that of the secondary amide agent.
41. The gasket of claim 36, wherein the slip agent comprises a silane compound.
42. The gasket of claim 36, wherein the gasket is foamed using a foaming agent.
43. The gasket of claim 42, wherein the foaming agent is selected from a group consisting of physical blowing agents, gaseous blowing agents and chemical blowing agents.
44. The gasket of claim 42, wherein the foaming agent is a chemical blowing agent selected from a group consisting of sodium bicarbonate, 127 dinitrosopentamethylenetetramine, sulfonyl hydrazides, azodicarbonamide, p-toluenesulfonyl semicarbazide, 5-phenyltetrazole, diisopropylhydrazodicarboxylate, 5-phenyl-3,6-dihydro- l,3,4-oxadiazin-2-one, and sodium borohydride.
45. The gasket of claim 42, wherein the foaming agent is a gaseous blowing agent selected from the group consisting of carbon dioxide and nitrogen.
46. The gasket of claim 43, wherein the foaming agent is a physical blowing agent selected from a group consisting of pentanes, hexanes, heptanes, benzene, toluene, dichloromethane, trichloromethane, trichloroethylene, tetrachloromethane, 1,2- dichloroethane, trichlorofluoromethane, 1,1,2-trichlorotrifluoroethane, methanol, ethanol, 2- propanol, ethyl ether, isopropyl ether, acetone, methyl ethyl ketone, and methylene chloride; isobutane and n-butane, 1,1-difluoroethane.
47. The gasket of claim 36, wherein the ethelyne/α-olefin interpolymer comprises from about 25 to about 35% by weight of the composition, the other polymer comprises from about 55 to about 65 % by weight of the composition, and the slip agent comprises from about 1 to about 3 % by weight of the composition.
48. The gasket of claim 36, wherein the composition has either a static coefficient of friction or a dynamic coefficient of friction, or both, of less than about 1.
49. The gasket of claim 36, wherein the composition has either a static coefficient of friction or a dynamic coefficient of friction, or both, of about 0.6 or less.
50. The gasket of claim 36, wherein the compostion has a melt index greater than or equal to about 5 g/10 minutes and a 7O0C compression set of less than 70% and the change is compression set between 230C and 7O0C is less that 55%.
51. The composition of claim 31 , wherein a gasket made from the composition is free of odor.
52. The composition of claim 31 , wherein the extender is a substantially linear ethylene polymer having a melt index, I2, from about 100 to about 1,000.
53. The composition of claim 27, wherein the styrenic block copolymer is a SEBS block copolymer with a melt index of less than 0.1.
54. A process for preparing a synthetic cork closure for a liquid container having at least a portion thereof coated with a gas impermeable polymer which comprises providing a synthetic cork closure and coating at least a portion thereof with a gas impermeable polymer, wherein the synthetic closure comprises a composition comprising: 128
(A) about 80 to about 97.5 weight percent, based on the total weight of components (A), (B) and (C), of at least one ethylene/α-olefin interpolymer; wherein the ethylene/α-olefϊn interpolymer is a block interpolymer and:
(a) has a Mw/Mn from about 1.7 to about 3.5, at least one melting point, Tm, in degrees Celsius, and a density, d, in grams/cubic centimeter, wherein the numerical values of Tm and d correspond to the relationship:
Tm > -2002.9 + 4538.5(d) - 2422.2(d)2, or
(b) has a Mw/Mn from about 1.7 to about 3.5, and is characterized by a heat of fusion, ΔH in J/g, and a delta quantity, ΔT, in degrees CelsiuSj defined as the temperature difference between the tallest DSC peak and the tallest CRYSTAF peak, wherein the numerical values of ΔT and ΔH have the following relationships:
ΔT > -0.1299(ΔH) + 62.81 for ΔH greater than zero and up to 130 J/g, ΔT > 480C for ΔH greater than 130 J/g , wherein the CRYSTAF peak is determined using at least 5 percent of the cumulative polymer, and if less than 5 percent of the polymer has an identifiable CRYSTAF peak, then the CRYSTAF temperature is 3O0C; or
(c) is characterized by an elastic recovery, Re, in percent at 300 percent strain and 1 cycle measured with a compression-molded film of the ethylene/α- olefin interpolymer, and has a density, d, in grams/cubic centimeter, wherein the numerical values of Re and d satisfy the following relationship when ethylene/α-olefin interpolymer is substantially free of a cross-linked phase:
Re >1481-1629(d); or
(d) has a molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a molar comonomer content of at least 5 percent higher than that of a comparable random ethylene interpolymer fraction eluting between the same temperatures, wherein said comparable random ethylene interpolymer has the same comonomer(s) and has a melt index, density, and molar comonomer content (based on the whole polymer) within 10 percent of that of the ethylene/α-olefin interpolymer; or (e) has a storage modulus at 250C, G' (250C), and a storage modulus at 1000C, C(IOO0C), wherein the ratio of G'(25°C) to G'(100°C) is in the range of about 1:1 to about 9:1; or
(f) at least one molecular fraction which elutes between 4O0C and 13O0C when fractionated using TREF, characterized in that the fraction has a block index of at least 0.5 and up to about 1 and a molecular weight distribution, Mw/Mn, greater than about 1.3; or
(g) an average block index greater than zero and up to about 1.0 and a molecular weight distribution, Mw/Mn, greater than about 1.3.
PCT/US2006/009501 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers WO2006113000A2 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
AU2006237514A AU2006237514B2 (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers
JP2008502036A JP5227786B2 (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers
BRPI0609824-0A BRPI0609824B1 (en) 2005-03-17 2006-03-15 POLYMERIC MIXTURE AND GASKET COMPOSITION
CA002601263A CA2601263A1 (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers
MX2007011334A MX2007011334A (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers.
CN2006800083690A CN101426880B (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers
US11/908,951 US7592397B2 (en) 2005-03-17 2006-03-15 Cap liners, closures, and gaskets from multi-block polymers
EP06769781.3A EP1877513B1 (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
USPCT/US2005/008917 2005-03-17
PCT/US2005/008917 WO2005090427A2 (en) 2004-03-17 2005-03-17 Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation
US71782405P 2005-09-16 2005-09-16
US60/717,824 2005-09-16

Publications (3)

Publication Number Publication Date
WO2006113000A2 WO2006113000A2 (en) 2006-10-26
WO2006113000A3 WO2006113000A3 (en) 2007-10-11
WO2006113000B1 true WO2006113000B1 (en) 2007-12-06

Family

ID=36928316

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/009501 WO2006113000A2 (en) 2005-03-17 2006-03-15 Cap liners, closures and gaskets from multi-block polymers

Country Status (12)

Country Link
US (1) US7592397B2 (en)
EP (1) EP1877513B1 (en)
JP (1) JP5227786B2 (en)
CN (1) CN101426880B (en)
AR (1) AR054017A1 (en)
AU (1) AU2006237514B2 (en)
BR (1) BRPI0609824B1 (en)
CA (1) CA2601263A1 (en)
MX (1) MX2007011334A (en)
MY (1) MY142099A (en)
TW (1) TW200635961A (en)
WO (1) WO2006113000A2 (en)

Families Citing this family (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2008143990A (en) * 2006-04-06 2010-05-20 Дау Глобал Текнолоджиз, Инк. (Us) ADHESION-MODIFIED FOAMABLE POLYOLEFIN COMPOSITIONS AND INSULATED PARTS OF VEHICLES CONTAINING FOAMED ADHESION-MODIFIED POLYOLEFIN COMPOSITIONS
WO2007136552A2 (en) * 2006-05-09 2007-11-29 Jeffrey Jacob Cernohous Compatibilized polymer processing additives
US9187631B2 (en) 2007-10-22 2015-11-17 Trinseo Europe Gmbh Polymeric compositions and processes for molding articles
EP2058379A1 (en) 2007-11-09 2009-05-13 ACTEGA DS GmbH Method for manufacturing a closure
US20090274856A1 (en) * 2008-05-01 2009-11-05 Chou Richard T Compositions comprising ethylene acid copolymers and functional ethylene copolymers
FR2937046B1 (en) * 2008-10-15 2012-10-19 Vallourec Mannesmann Oil & Gas ADJUSTABLE FRICTION COEFFICIENT LUBRICATION COMPOSITION FOR A THREADED ELEMENT OF A TUBULAR THREADED COMPONENT
EP2342239B1 (en) * 2008-10-31 2020-04-15 Performance Materials NA, Inc. High-clarity ionomer compositions and articles comprising the same
EP2376549B1 (en) 2008-12-30 2013-12-25 E. I. du Pont de Nemours and Company High-clarity blended ionomer compositions and articles comprising the same
WO2010077425A1 (en) * 2008-12-31 2010-07-08 E. I. Du Pont De Nemours And Company Solar cell modules comprising encapsulant sheets with low haze and high moisture resistance
JP5587336B2 (en) * 2008-12-31 2014-09-10 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Ionomer composition with low haze and high waterproofness and article containing the same
US8399098B2 (en) * 2008-12-31 2013-03-19 E I Du Pont De Nemours And Company Laminates comprising ionomer interlayers with low haze and high moisture resistance
ES2619520T5 (en) * 2009-11-20 2020-09-28 Actega Ds Gmbh Polymeric compound for sealing gaskets for products with fat content to be packaged
US20110178245A1 (en) * 2010-01-15 2011-07-21 Tredegar Film Products Corporation Elastic Blends of High Density Polyethylene Polymers with Olefinic Block Copolymers
US8853289B2 (en) 2010-05-18 2014-10-07 Scott C. Smith Foam compositions for selective recovery of oil spills and other applications
ES2538976T3 (en) * 2010-06-14 2015-06-25 Dow Global Technologies Llc Copolymer composition of low adhesion olefin blocks
FR2961517B1 (en) * 2010-06-18 2014-04-11 Thermoplastiques Cousin Tessier RETICULATED ELASTOMERIC COMPOSITION AND PRODUCT COMPRISING SUCH A COMPOSITION
EP2402391B1 (en) * 2010-06-29 2013-07-31 Borealis AG Bimodal polyethylene composition for injection moulded articles
FR2966191B1 (en) * 2010-10-15 2013-11-01 Vallourec Mannesmann Oil & Gas TUBULAR THREADED COMPONENT AND RESULTING SEAL
JP2012149761A (en) * 2010-12-28 2012-08-09 Kitz Corp Needle valve and o-ring
US20120247607A1 (en) * 2011-03-31 2012-10-04 Ufp Technologies, Inc. Sanitary cap and system
FI3699251T3 (en) * 2011-05-11 2023-10-13 Actega Ds Gmbh Pvc-free closures
US8962723B2 (en) * 2011-06-15 2015-02-24 Lion Copolymer Geismar, Llc Durable substrate coating and process for making
WO2013101301A2 (en) 2011-06-17 2013-07-04 Berry Plastics Corporation Insulated sleeve for a cup
WO2012174568A2 (en) 2011-06-17 2012-12-20 Berry Plastics Corporation Process for forming an insulated container having artwork
WO2012174422A2 (en) 2011-06-17 2012-12-20 Berry Plastics Corporation Insulated container with molded brim
DE202012013293U1 (en) 2011-06-17 2016-01-15 Berry Plastics Corporation Isolated container
JP6096772B2 (en) * 2011-07-22 2017-03-15 パックサイズ,エルエルシー Tiling production of packaging materials
KR20140059255A (en) 2011-08-31 2014-05-15 베리 플라스틱스 코포레이션 Polymeric material for an insulated container
CN103958548B (en) 2011-12-02 2016-05-18 住友化学株式会社 Use the manufacture method of the olefin block polymers of multiple transition-metal catalyst
US10549893B2 (en) 2011-12-22 2020-02-04 G3 Enterprises, Inc. Method for controlling oxygen ingress in cap closure
EP2794412B1 (en) 2011-12-22 2020-08-12 G3 Enterprises, Inc. Cap closure and method for controlling oxygen ingress in cap closure
CN104245835B (en) * 2012-03-30 2017-02-22 陶氏环球技术有限责任公司 polyolefin elastomer formulations
US9975982B2 (en) 2012-06-29 2018-05-22 Dow Global Technologies Llc Stain resistant article with olefin block copolymer and process
BR112015002581A2 (en) 2012-08-07 2018-05-22 Berry Plastics Corp cup forming machine and process.
WO2014066761A1 (en) 2012-10-26 2014-05-01 Berry Plastics Corporation Polymeric material for an insulated container
AR093944A1 (en) 2012-12-14 2015-07-01 Berry Plastics Corp PUNCHED FOR PACKAGING
US9840049B2 (en) 2012-12-14 2017-12-12 Berry Plastics Corporation Cellular polymeric material
AR093943A1 (en) 2012-12-14 2015-07-01 Berry Plastics Corp EDGE OF A THERMAL PACK
US9493275B2 (en) 2013-01-03 2016-11-15 Empire Technology Development Llc Resealable containers and methods for their preparation and use
US9447269B2 (en) * 2013-01-18 2016-09-20 Dow Global Technologies Llc Modified flexible EVOH for high performance films
US8901201B2 (en) * 2013-02-13 2014-12-02 Lion Copolymer Geismar, Llc Method for making an ambient light curable ethylene propylene diene terpolymer rubber coating devoid of thermally activated accelerators
US9957365B2 (en) 2013-03-13 2018-05-01 Berry Plastics Corporation Cellular polymeric material
CA2843864C (en) * 2013-03-14 2020-09-08 Nova Chemicals Corporation Hinge polymer
US9725202B2 (en) 2013-03-14 2017-08-08 Berry Plastics Corporation Container
MX363704B (en) * 2013-04-18 2019-03-29 Dow Global Technologies Llc Films containing extrudable adhesive formulations.
US9562140B2 (en) 2013-08-16 2017-02-07 Berry Plastics Corporation Polymeric material for an insulated container
CA2938295C (en) * 2014-01-28 2022-08-16 G3 Enterprises, Inc. System and method for implementing cap closure for carbonated and oxygen sensitive beverages
JP6339382B2 (en) * 2014-03-05 2018-06-06 コリア ミンティング,セキュリティ プリンティング アンド アイディ カード オペレーティング コーポレーション Security film
CA2844886C (en) * 2014-03-06 2020-09-01 Nova Chemicals Corporation Radiation crosslinked polyethylene hinge
JP6253765B2 (en) 2014-03-28 2017-12-27 三井化学株式会社 Olefin resin and process for producing the same
US9758655B2 (en) 2014-09-18 2017-09-12 Berry Plastics Corporation Cellular polymeric material
CN104326148A (en) * 2014-09-29 2015-02-04 无锡华鹏瓶盖有限公司 PVC-free type claw type unscrewing cover manufacturing process for medicine package
EP3009461A1 (en) * 2014-10-13 2016-04-20 Sika Technology AG Polyester prepolymers as a toughener in epoxy formulations
WO2016093266A1 (en) 2014-12-09 2016-06-16 三井化学株式会社 Propylene-based resin composition
US10513589B2 (en) 2015-01-23 2019-12-24 Berry Plastics Corporation Polymeric material for an insulated container
JP6165192B2 (en) * 2015-05-22 2017-07-19 ダウ グローバル テクノロジーズ エルエルシー Thermoplastic elastomers for low temperature and wet applications
CN107636064B (en) * 2015-05-26 2019-05-03 巴塞尔聚烯烃意大利有限公司 Polyolefin washer for capping
CN107709442A (en) * 2015-06-30 2018-02-16 陶氏环球技术有限责任公司 Admixture for foam, the foam being produced from it and the product comprising foam
CN107847870B (en) * 2015-07-09 2021-09-07 恩特格里斯公司 Mixed potting resin and application thereof
EP3181635A1 (en) * 2015-12-18 2017-06-21 Borealis AG A compounded polyethylene composition, process for its manufacturing and articles comprising it
WO2017112510A1 (en) 2015-12-21 2017-06-29 Dow Global Technologies Llc Polyethylene formulations with improved barrier and environmental stress crack resistance
EP3185335B1 (en) * 2015-12-21 2020-02-05 The Swatch Group Research and Development Ltd. Battery
WO2017112503A2 (en) 2015-12-21 2017-06-29 Dow Global Technologies Llc Polyethylene formulations with improved barrier and toughness for molding applications
EP3430066B1 (en) * 2016-03-14 2023-02-22 Dow Global Technologies LLC Process for preparing foamed articles made from ethylene/alpha-olefin interpolymers
BR112019006200B1 (en) * 2016-09-29 2022-08-02 Dow Global Technologies Llc FOAM COMPOSITION, ARTICLE AND MANUFACTURING METHOD OF A FOAM COMPOSITION
CN106496914A (en) * 2016-10-27 2017-03-15 福州大学 Composite foamed material for shoes of a kind of OBC/LDPE and preparation method thereof
KR102573484B1 (en) 2016-11-17 2023-09-04 현대자동차주식회사 Polyolefine resin composition, polyolefine master batch, process of polyolefine master batch and article using thereof
CN106589631A (en) * 2016-11-22 2017-04-26 日丰企业集团有限公司 Surface scratch resistant polybutene pipe and preparation method thereof
CN106763358A (en) * 2016-12-06 2017-05-31 周潇潇 A kind of anticorrosive anti-wear brake pad material
JP6198182B1 (en) * 2016-12-09 2017-09-20 三菱瓦斯化学株式会社 Multilayer body, packaging container, and food storage method
CN107177090B (en) * 2017-07-05 2020-10-27 特步(中国)有限公司 Nylon foamed shoe material and manufacturing method thereof
US11091311B2 (en) 2017-08-08 2021-08-17 Berry Global, Inc. Insulated container and method of making the same
JP6921719B2 (en) * 2017-11-17 2021-08-18 日本クロージャー株式会社 Composition for cap liner
US20190183093A1 (en) * 2017-12-17 2019-06-20 Oleksandr Skoropys Training device for animals
CN111630100B (en) * 2018-01-22 2023-02-03 三井—陶氏聚合化学株式会社 Sealing resin composition, sealing material, packaging container, and package
FR3078070B1 (en) * 2018-02-20 2020-01-24 Urgo Recherche Innovation Et Developpement COMPOSITION HAVING EXCELLENT WATER VAPOR PERMEABILITY
EP3788104A1 (en) 2018-05-03 2021-03-10 Dow Global Technologies LLC Propylene-based polymer compositions with excellent flexibility and hot air weldability
CN109627531B (en) * 2018-12-06 2021-04-20 安徽中斯特流体设备有限公司 Sealing gasket for valve without cracking easily
KR102323503B1 (en) * 2019-03-04 2021-11-09 코스파 주식회사 eco-friendly Foam and method for producing the same
DE112020001702T5 (en) * 2019-04-04 2021-12-16 Sumitomo Electric Industries, Ltd. Electrical insulation composition and power cables
CN113727852A (en) 2019-04-17 2021-11-30 日东电工株式会社 Multi-layer coextruded film and articles including the same
EP3988296A4 (en) 2019-06-24 2023-07-19 Japan Polyethylene Corporation Resin for film-shaped molded body, and molded article comprising said resin
CN110317388B (en) * 2019-07-18 2023-04-07 奥星衡迅生命科技(上海)有限公司 Packaging material directly contacted with medicine and preparation method and application thereof
JP7075921B2 (en) * 2019-12-27 2022-05-26 株式会社アシックス Buffer and shoes
WO2021188361A1 (en) 2020-03-20 2021-09-23 Exxonmobil Chemical Patents Inc. Linear alpha-olefin copolymers and impact copolymers thereof
JP7014361B2 (en) * 2020-06-25 2022-02-01 ダウ グローバル テクノロジーズ エルエルシー Blends for foams, foams produced from them and articles containing them
WO2024073577A1 (en) 2022-09-30 2024-04-04 Dow Global Technologies Llc Polyolefin compositions with excellent impact strength and light transmittance

Family Cites Families (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3873642A (en) * 1961-02-20 1975-03-25 Avisun Corp Crystalline olefin block polymers and their preparation
US4798081A (en) * 1985-11-27 1989-01-17 The Dow Chemical Company High temperature continuous viscometry coupled with analytic temperature rising elution fractionation for evaluating crystalline and semi-crystalline polymers
EP0274906B1 (en) 1986-12-26 1993-02-17 Mitsubishi Petrochemical Co., Ltd. Method for the production of crosslinked olefinic block copolymers
GB2241244B (en) * 1990-02-22 1994-07-06 James C W Chien Thermoplastic elastomers
JPH0790035A (en) * 1993-07-27 1995-04-04 Ube Ind Ltd Production of propylene block copolymer
US5929128A (en) * 1993-08-18 1999-07-27 The Dow Chemical Company Gaskets made from olefin polymers
EP0714427B1 (en) * 1993-08-18 1999-06-16 The Dow Chemical Company Gaskets made from homogeneous linear olefin polymers
US5594080A (en) * 1994-03-24 1997-01-14 Leland Stanford, Jr. University Thermoplastic elastomeric olefin polymers, method of production and catalysts therefor
KR970702306A (en) * 1994-04-06 1997-05-13 카덴헤드 벤 씨 Ethylene α-olefin block copolymers and a method for preparing the same (ETHYLENE ALPHA-OLEFIN BLOCK COPOLYMERS AND METHODS FOR PRODUCTION THEREOF)
WO1995027746A1 (en) 1994-04-06 1995-10-19 Exxon Chemical Patents Inc. ETHYLENE α-OLEFIN BLOCK COPOLYMERS AND METHODS FOR PRODUCTION THEREOF
DE4425408A1 (en) * 1994-07-13 1996-01-18 Hoechst Ag cycloolefin
US6576306B2 (en) * 1996-09-04 2003-06-10 Exxonmobil Chemical Patents Inc. Propylene polymers for films
US6114457A (en) * 1997-02-07 2000-09-05 Exxon Chemical Patents Inc. High melt strength polyethylene compositions
KR100564500B1 (en) 1997-02-07 2006-03-29 엑손모빌 케미칼 패턴츠 인코포레이티드 Propylene polymers incorporating polyethylene macromers
WO1999035171A1 (en) 1998-01-09 1999-07-15 The Board Of Trustees Of The Leland Stanford Jr. University High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis
ATE384747T1 (en) 1998-12-21 2008-02-15 Exxonmobil Chem Patents Inc METHOD FOR PRODUCING BRANCHED ETHYLENE-PROPYLENE COPOLYMERS
TW524825B (en) * 1999-07-13 2003-03-21 Chisso Corp Polyolefin resin composition
JP3404368B2 (en) * 1999-11-04 2003-05-06 日東電工株式会社 Adhesive tape
US6160029A (en) * 2000-03-08 2000-12-12 The Dow Chemical Company Olefin polymer and α-olefin/vinyl or α-olefin/vinylidene interpolymer blend foams
US6455638B2 (en) * 2000-05-11 2002-09-24 Dupont Dow Elastomers L.L.C. Ethylene/α-olefin polymer blends comprising components with differing ethylene contents
JP2002206007A (en) 2000-11-08 2002-07-26 National Institute Of Advanced Industrial & Technology Method for manufacturing olefinic block copolymer
EP1373367A2 (en) 2001-01-10 2004-01-02 Basell Poliolefine Italia S.p.A. Block copolymers and process for their preparation
EP1375585B1 (en) * 2001-03-29 2005-12-21 Idemitsu Kosan Co., Ltd. Propylene polymer composition, molded object, and polyolefin copolymer
US7022766B2 (en) * 2001-05-31 2006-04-04 Mitsui Chemicals, Inc. Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition
SG120869A1 (en) 2001-05-31 2006-04-26 Mitsui Chemicals Inc Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition
DE10127926A1 (en) * 2001-06-08 2002-12-12 Bayer Ag 1,3-disubstituted indene complexes
US7087686B2 (en) 2001-08-06 2006-08-08 Bp Chemicals Limited Chain growth reaction process
JP2005508415A (en) * 2001-11-06 2005-03-31 ダウ グローバル テクノロジーズ インコーポレイティド Isotactic propylene copolymers, their production and use
JP2004204058A (en) 2002-12-25 2004-07-22 Mitsui Chemicals Inc Olefin-based block copolymer
US7906586B2 (en) * 2003-12-09 2011-03-15 Dow Global Technologies Llc Thermoplastic olefinic compositions
US7687442B2 (en) * 2004-03-17 2010-03-30 Dow Global Technologies Inc. Low molecular weight ethylene/α-olefin interpolymer as base lubricant oils
US7803728B2 (en) * 2004-03-17 2010-09-28 Dow Global Technologies Inc. Fibers made from copolymers of ethylene/α-olefins
EP1727840B1 (en) * 2004-03-17 2012-10-24 Dow Global Technologies LLC Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation
US7557147B2 (en) * 2004-03-17 2009-07-07 Dow Global Technologies Inc. Soft foams made from interpolymers of ethylene/alpha-olefins
US7662881B2 (en) * 2004-03-17 2010-02-16 Dow Global Technologies Inc. Viscosity index improver for lubricant compositions
WO2005090427A2 (en) * 2004-03-17 2005-09-29 Dow Global Technologies Inc. Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation
US7582716B2 (en) * 2004-03-17 2009-09-01 Dow Global Technologies Inc. Compositions of ethylene/α-olefin multi-block interpolymer for blown films with high hot tack
AR053693A1 (en) * 2004-03-17 2007-05-16 Dow Global Technologies Inc COMPOSITIONS OF ETHYLENE / ALFA-OLEFINE INTERPOLIMERO MULTIBLOCK SUITABLE FOR FILMS
US7504347B2 (en) * 2004-03-17 2009-03-17 Dow Global Technologies Inc. Fibers made from copolymers of propylene/α-olefins
US7671131B2 (en) * 2004-03-17 2010-03-02 Dow Global Technologies Inc. Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom
US7741397B2 (en) * 2004-03-17 2010-06-22 Dow Global Technologies, Inc. Filled polymer compositions made from interpolymers of ethylene/α-olefins and uses thereof
US7622179B2 (en) * 2004-03-17 2009-11-24 Dow Global Technologies Inc. Three dimensional random looped structures made from interpolymers of ethylene/α-olefins and uses thereof
US7714071B2 (en) * 2004-03-17 2010-05-11 Dow Global Technologies Inc. Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom
US7897689B2 (en) * 2004-03-17 2011-03-01 Dow Global Technologies Inc. Functionalized ethylene/α-olefin interpolymer compositions
US7795321B2 (en) * 2004-03-17 2010-09-14 Dow Global Technologies Inc. Rheology modification of interpolymers of ethylene/α-olefins and articles made therefrom
US7514517B2 (en) * 2004-03-17 2009-04-07 Dow Global Technologies Inc. Anti-blocking compositions comprising interpolymers of ethylene/α-olefins
US7671106B2 (en) * 2004-03-17 2010-03-02 Dow Global Technologies Inc. Cap liners, closures and gaskets from multi-block polymers
AR048817A1 (en) * 2004-03-17 2006-05-31 Dow Global Technologies Inc CATALYST COMPOSITION THAT INCLUDES LINK AGENT FOR THE FORMATION OF COPOLYMERS OF MULTIPLE ETHYLENE BLOCKS
US7666918B2 (en) * 2004-03-17 2010-02-23 Dow Global Technologies, Inc. Foams made from interpolymers of ethylene/α-olefins
US7622529B2 (en) * 2004-03-17 2009-11-24 Dow Global Technologies Inc. Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility
US7524911B2 (en) * 2004-03-17 2009-04-28 Dow Global Technologies Inc. Adhesive and marking compositions made from interpolymers of ethylene/α-olefins
EP1650297B1 (en) * 2004-10-19 2011-04-13 Samsung Electronics Co., Ltd. Method and apparatus for the rapid disruption of cells or viruses using micro magnetic beads and laser
JP5231984B2 (en) * 2005-03-17 2013-07-10 ダウ グローバル テクノロジーズ エルエルシー Polymer blends made from ethylene / α-olefin copolymers with improved compatibility

Also Published As

Publication number Publication date
BRPI0609824B1 (en) 2022-09-27
WO2006113000A2 (en) 2006-10-26
US20080269388A1 (en) 2008-10-30
MY142099A (en) 2010-09-15
BRPI0609824A2 (en) 2010-04-27
CA2601263A1 (en) 2006-10-26
CN101426880B (en) 2013-10-30
US7592397B2 (en) 2009-09-22
EP1877513B1 (en) 2019-05-08
AU2006237514B2 (en) 2011-10-27
AU2006237514A1 (en) 2006-10-26
JP2008545017A (en) 2008-12-11
CN101426880A (en) 2009-05-06
MX2007011334A (en) 2007-10-02
EP1877513A2 (en) 2008-01-16
TW200635961A (en) 2006-10-16
JP5227786B2 (en) 2013-07-03
WO2006113000A3 (en) 2007-10-11
AR054017A1 (en) 2007-05-30

Similar Documents

Publication Publication Date Title
WO2006113000B1 (en) Cap liners, closures and gaskets from multi-block polymers
RU2007134343A (en) CAP LINES, COVERS AND SEALS FROM CELLULAR POLYMERS
CA2245735C (en) Foamed gaskets made from homogeneous olefin polymers
US4918111A (en) Composition for non-crosslinked foam
JP2008545017A5 (en)
CA2470650A1 (en) Multimodal polymeric foam containing an absorbent clay
WO2001064784A1 (en) Thermoplastic elastomer composition, foam made from the same, and process for producing foam
WO2006101932B1 (en) FILLED POLYMER COMPOSITIONS MADE FROM INTERPOLYMERS OF ETHYLENE/α-OLEFINS AND USES THEREOF
JP2008533289A5 (en)
CA1279440C (en) Non-crosslinked foam
JP5075046B2 (en) Foam sheet
EP0579249B1 (en) Process for repairing plastic coatings on metal pipes
CN101746547B (en) Modified asphalt wrapping film bag and preparation method thereof
JP2004277986A (en) Wallpaper and method for producing the same
TW200904632A (en) Batch inclusion packages
JP4949728B2 (en) Resin composition for foam molding and molded product obtained therefrom
KR101921682B1 (en) Elastomeric composite for impact absorption
CN115304844A (en) High-density polyethylene waterproof sheet, preparation method and high-density polyethylene waterproof coiled material
JPH061874A (en) Preexpanded polyethylene resin particle
JP3227831B2 (en) Compositions for floor, ceiling and wall facings
JP2005220303A (en) Polypropylene-based resin composition for forming foamed article and peroxide-cross-linked foamed article consisting of the same
JP2003026870A (en) Polyethylene resin composition, polyethylene resin composition for foaming and foamed product
JP4369311B2 (en) Soft film and its use
JP2002019028A (en) Foamed polyolefin laminate
JP2006249350A (en) Resin composition for foam molding and foamed molded article formed from the same

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200680008369.0

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application
ENP Entry into the national phase

Ref document number: 2601263

Country of ref document: CA

Ref document number: 2008502036

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 561536

Country of ref document: NZ

Ref document number: MX/a/2007/011334

Country of ref document: MX

Ref document number: 2007134343

Country of ref document: RU

Ref document number: 07095055

Country of ref document: CO

Ref document number: 4043/CHENP/2007

Country of ref document: IN

Ref document number: 2006769781

Country of ref document: EP

Ref document number: 1020077021163

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2006237514

Country of ref document: AU

NENP Non-entry into the national phase

Ref country code: DE

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
ENP Entry into the national phase

Ref document number: 2006237514

Country of ref document: AU

Date of ref document: 20060315

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 11908951

Country of ref document: US

ENP Entry into the national phase

Ref document number: PI0609824

Country of ref document: BR

Kind code of ref document: A2