WO2015168328A1 - Polymer foams - Google Patents
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- WO2015168328A1 WO2015168328A1 PCT/US2015/028359 US2015028359W WO2015168328A1 WO 2015168328 A1 WO2015168328 A1 WO 2015168328A1 US 2015028359 W US2015028359 W US 2015028359W WO 2015168328 A1 WO2015168328 A1 WO 2015168328A1
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- peroxydicarbonate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
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- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0052—Organo-metallic compounds
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- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08K5/00—Use of organic ingredients
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- C08K5/14—Peroxides
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions 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
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/12—Melt flow index or melt flow ratio
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/06—CO2, N2 or noble gases
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/16—Unsaturated hydrocarbons
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised 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
- C08J2323/04—Homopolymers or copolymers of ethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised 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
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/12—Polypropene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
- C08J2325/04—Homopolymers or copolymers of styrene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—Characterised 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
- C08J2423/04—Homopolymers or copolymers of ethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2467/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2471/02—Polyalkylene oxides
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0023—Use of organic additives containing oxygen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
Definitions
- Embodiments of the present disclosure generally to foams made from polymers.
- Polymers may be used for various foamed applications, particularly for applications requiring lightweight energy management or cushioning. Examples include automotive components, packaging, dunnage, thermal insulation, and safety applications where repeated impact may occur.
- An embodiment of the present disclosure includes polymer composition.
- the polymer composition includes a polyolefin having a molecular weight distribution of greater than or equal to 8 as measured by GPC and a metallic acrylate salt.
- Another embodiment of the present disclosure includes a process.
- the process includes supplying a polymer composition which includes a polyolefin resin having a molecular weight distribution of greater than or equal to 8 as measured by GPC and a metallic acrylate salt.
- the process further includes mixing polymer composition and the foaming agent to form a polymer foam.
- Polymers useful in this disclosure include styrenic polymers and polyolefins.
- polyolefins include, but are not limited to, polyethylene, polypropylene, polyolefin elastomers, and combinations thereof.
- Polyolefin elastomers include, but are not limited to polyisoprene, polybutadiene, chloroprene, butyl rubber, styrene butadiene, nitrile rubber, ethylene propylene rubber, epichlorohydrin rubber, polyacrylic rubber, silicone rubber, fluorosilicone rubber, fluoroelastomers, perfluoroelastomers, polyether block amides, chlorosulfonated polyethylene, and ethylene-vinyl acetate.
- polyolefins useful in the present disclosure include linear low density polyethylene, plastomers, high density polyethylenes, low density polyethylenes, medium density poly ethylenes, polypropylene and polypropylene copolymers, for example.
- the polymer may also include functionalized versions of the above, for instance maleated polypropylene.
- styrenic polymers include homopolymers of styrene, alpha-methyl styrene, vinyl toluene, p-methyl styrene, t-butyl styrene, o-chlorostyrene, vinyl pyridine, and any combinations thereof.
- Styrenic polymers may contain one or more comonomers.
- Non- limiting examples of such comonomers include a-methylstyrene; halogenated styrenes; alkylated styrenes; acrylonitrile; esters of methacrylic acid with alcohols having 1 to 8 carbons; N-vinyl compounds such as vinylcarbazole and maleic anhydride; compounds which contain two polymerizable double bonds such as for example and without limitation divinylbenzene or butanediol diacrylate; or combinations thereof.
- the styrenic polymer may include a thermoplastic material.
- thermoplastic materials include without limitation acrylonitrile butadiene styrene, celluloid, cellulose acetate, ethylene vinyl acetate, ethylene vinyl alcohol, fluoroplastics, ionomers, polyacetal, polyacrylates, polyacrylonitrile, polyamide, polyamide-imide, polyaryletherketone, polybutadiene, polybutylene, polybutylene terephthalate, polychlorotrifluoroethylene, polyethylene terephthalate, polycyclohexylene dimethylene terephthalate, polycarbonate, polyetherimide, polyethersulfone, polyethylenechlorinate, polyimide, polylactic acid, polymethylpentene, polyphenylene oxide, polyphenylene sulfide, polyphthalamide, polypropylene, polysulfone, polyvinyl chloride, polyvinylidene chloride, and combinations thereof.
- the styrenic polymer may include an elastomeric phase that is embedded in a polymer matrix.
- the elastomeric phase may include a conjugated diene monomer such as 1,3 -butadiene, 2-methyl-l,3- butadiene, and 2-chloro- 1,3 -butadiene, or an aliphatic conjugated diene monomer such as C 4 to C9 dienes such as butadiene monomers.
- the polyolefin is a propylene based polymer.
- the term "propylene based” is used interchangeably with the terms "propylene polymer” or “polypropylene” and refers to a polymer having at least about 50 wt.%, or at least about 70 wt.%, or at least about 75 wt.%, or at least about 80 wt.%, or at least about 85 wt.% or at least about 90 wt.% polypropylene relative to the total weight of polymer, for example.
- the polypropylene may be, for instance, a propylene homopolymer, a propylene random copolymer, a propylene impact copolymer, a syndiotactic polypropylene, isotactic polypropylene or atactic polypropylene.
- the propylene-based polymers may be a "mini-random" polypropylene.
- a mini-random polypropylene has less than about 1.0 wt% of the comonomer.
- the comonomer in the mini-random polypropylene is ethylene.
- the propylene based polymers may have a melting point (T m ) (as measured by DSC) of at least about 100°C, or from about 115°C to about 175°C, for example.
- T m melting point
- the propylene based polymers may include about 15 wt.% or less, or about 12 wt.% or less, or about 10 wt.% or less, or about 6 wt.% or less, or about 5 wt.% or less or about 4 wt.% or less of xylene soluble material (XS), for example (as measured by ASTM D5492-06).
- XS xylene soluble material
- the propylene based polymers may have a molecular weight distribution (M w /M n ) of from about 2 to about 50, from about 6 to about 30 or greater than or equal to 8, for example, as measured by GPC.
- M w /M n molecular weight distribution
- These propylene based polymers may have a melt flow rate (MFR) (as measured by ASTM D-1238) of from about 0.01 dg/min to about 20 dg/min., or from about 0.01 dg/min. to about 10 dg/min., or less than 10 dg/min, for example.
- MFR melt flow rate
- the polymers include ethylene based polymers.
- ethylene based is used interchangeably with the terms "ethylene polymer” or “polyethylene” and refers to a polymer having at least about 50 wt.%, or at least about 70 wt.%, or at least about 75 wt.%, or at least about 80 wt.%, or at least about 85 wt.% or at least about 90 wt.% polyethylene relative to the total weight of polymer, for example.
- the ethylene based polymers may have a density (as measured by ASTM D-792) of from about 0.86 g/cc to about 0.98 g/cc, or from about 0.88 g/cc to about 0.965 g/cc, or from about 0.90 g/cc to about 0.965 g/cc or from about 0.925 g/cc to about 0.97 g/cc, for example.
- the ethylene based polymers may have a melt index (MI2) (as measured by ASTM D-1238) of from about 0.01 dg/min to about 1000 dg/min., or from about 0.01 dg/min. to about 25 dg/min., or from about 0.03 dg/min. to about 15 dg/min. or from about 0.05 dg/min. to about 10 dg/min, for example.
- MI2 melt index
- the olefin based polymers include low density polyethylene. In one or more embodiments, the olefin based polymers include linear low density polyethylene. In one or more embodiments, the olefin based polymers include medium density polyethylene. As used herein, the term "medium density polyethylene” refers to ethylene based polymers having a density of from about 0.92 g/cc to about 0.94 g/cc or from about 0.926 g/cc to about 0.94 g/cc, for example, as measured by ASTM D-792.
- the olefin based polymers include high density polyethylene.
- high density polyethylene refers to ethylene based polymers having a density of from about 0.94 g/cc to about 0.97 g/cc, for example, as measured by ASTM D-792.
- a mixture of one or more olefin based polymers may be used.
- the polyolefin may be combined with one or more ionomers to form a polymer composition.
- the ionomer may include functionalized organometallic compounds such as an organometallic salt having acrylate functional groups, termed a "metallic acrylate salt," for example.
- metallic acrylate salts are metallic diacrylates, such as zinc diacrylate, zinc dimethylacrylate, copper diacrylate, copper dimethylacrylate.
- organometallic salts include zinc di- vinylacetate, zinc di-ethylfumarate, copper di-vinylacetate, copper diethylefumarate, aluminum triacrylate, aluminum trimethylacrylate, aluminum tri-vinylacetate, aluminum tri- ethylfumarate, zirconium tetraacrylate, zirconium tetramethylacrylate, zirconium tetra- vinylacetate, zirconium tetra-ethyl fumarate, sodium acrylate, sodium methacrylate, and silver methacrylate.
- Dymalink 9200 (formerly SR732) or Dymalink 9201, both of which are commercially available from Cray Valley Specialty Chemicals.
- Dymalink 9200 is available as a white powder having a molecular weight of about 207 g/mol.
- Dymalink 9201 includes the metallic diacrylate in a pellet concentrate.
- the polymer composition of the polymer and ionomer may include between 0.001 and 8 wt% of the ionomer, between 0.01 and 6 wt% of the ionomer, or less than or equal to 5 wt% of the ionomer.
- an additive may be combined with the polymer composition.
- the additive may be a peroxydicarbonate peroxide.
- the peroxydicarbonate peroxide may have the general structure of ROC(0)0-0(0)CORi wherein R and Ri represent alkyl and/or aryl groups.
- peroxydicarbonate peroxides include, but are not limited to di(4- tert-butylcyclohexyl) peroxydicarbonate, dicetyl peroxydicarbonate, dimyristyl peroxydicarbonate, diisopropyl peroxydicarbonate, isopropyl sec -butyl peroxydicarbonate, di-sec -butyl peroxydicarbonate, di(2-ethylhexyl) peroxydicarbonate, and mixtures thereof.
- the peroxydicarbonate peroxide may include between 0.001 and 3 wt% of the peroxydicarbonate peroxide, between 0.01 and 2.5 wt% of the peroxydicarbonate peroxide, or less than or equal to 2 wt% of the peroxydicarbonate peroxide.
- Mixing of the ionomer with the polymer may be performed by melt mixing using medium to high intensity mixing equipment including single and twin screw extruders, Banbury mixers, or roll mill provided the metallic acryalte salt is adequately dispersed. Temperatures utilized for mixing may be 30°C above the melting point of the polymer. In particular embodiments, the polymer/ionomer may be heated above 200°C, or between 200 - 260 °C. In certain embodiments of the present disclosure, such as when a peroxydicarbonate peroxide is used, the ionomer may be formed in situ, i.e., may be formed during the melt mixing process. For instance, in one embodiment, the ionomer may be formed by mixing zinc oxide with acrylic acid while mixing with the polymer.
- the additive may be a polar polymer, including, but not limited to polylactic acid, polycaprolactone, polyethylene glycol, or mixtures thereof.
- the polar polymer may be present in amounts of between .001 and 3 wt% of the polymer composition, between 0.01 and 2.5 wt% of the polymer composition, or less than or equal to 2 wt% of the polymer composition.
- both the peroxydicarbonate peroxide and the polar polymer may be present in the polymer composition.
- the additive may be a non-polar polymer, such as a polyolefin different from that of the polymer composition.
- a non-polar polymer such as a polyolefin different from that of the polymer composition.
- examples include, but are not limited to, polypropylene and polyethylene.
- the non-polar polymer may be physically blended or chemically mixed with the polymer of the polymer composition, i.e., the non- polar polymer may be manufactured in conjunction with the polymer of the polymer composition during formation of the polymer of the polymer composition in one or more reactors, or the non-polar polymer may be physically blended, such as by single and twin screw extruders, Banbury mixers, or roll mills.
- the polymer composition may contain additives such as antioxidants, light stabilizers, acid scavengers, lubricants, antistatic additives, nucleating/clarifying agents, colorants, or combinations thereof.
- the additives are present in a quantity from 0.01 to 5 wt%, optionally from 0.1 to 3 wt%, optionally from 0.5 to 2 wt%, in relation to the weight of the polymer composition.
- the polymer composition may be pelletized.
- the polymer compositions are useful in the manufacture of polymer foamed sheets or foamed polymeric layers in films (collectively referred to as "polymer foams" hereinafter).
- the polymer foam may be prepared from polymer composition and a foaming agent.
- the pelletized or unpelletized polymer composition may be combined with additives, such as antioxidants, light stabilizers, acid scavengers, lubricants, antistatic additives, nucleating/clarifying agents, colorants, or combinations thereof.
- the polymer composition may be of the type described previously herein.
- the foaming agent may be any foaming agent compatible with the other components of the polymer composition such as for example physical blowing agents, chemical blowing agents, and the like.
- Physical foaming agents are typically nonflammable gases that are able to evacuate the composition quickly leaving voids in the composition.
- Chemical foaming agents are chemical compounds that decompose endothermically at elevated temperatures. Decomposition of the chemical foaming agents generates gases that become entrained in the polymer composition, thus leading to the formation of voids within the polymer composition.
- Non-limiting examples of foaming agents suitable for use in this disclosure include without limitation pentane, isopentane carbon dioxide, nitrogen, water vapor, propane, n-butane, isobutane, n-pentane, 2,3-dimethylpropane, 1-pentene, cyclopentene, n-hexane, 2- methylpentane, 3-methylpentane, 2,3-dimethylbutane, 1-hexene, cyclohexane, n-heptane, 2- methylhexane, 2,2-dimethylpentane, 2,3-dimethylpentane, and combinations thereof.
- the foamed polymeric composition is prepared by contacting the polymer composition with the foaming agent, and thoroughly mixing the components for example by compounding or extrusion.
- the polymer composition is plasticized or melted by heating in an extruder and is contacted and mixed thoroughly with foaming agent.
- the polymer may be contacted with the foaming agent prior to introduction of the mixture to the extruder (e.g., via bulk mixing), during the introduction of the polymer composition to an extruder, or combinations thereof.
- the polymer foam sheet has a flexural modulus of between a flexural modulus of between 1.0 X 10 4 and 5.0 X 10 4 psi, 1.5 X 10 4 and 3.5 X 10 4 psi, or between 2.0 X 10 4 and 3.0 X 10 4 psi as measured by ASTM-D- 790.
- the flexural strength of the polymer foam sheet is between 500 and 1400 psi, between 600 and 1 100 psi, or between 700 and 1000 psi, as measured by ASTM-D-790.
- the polymer foam sheet has an open cell content of less than 80%, less than 50%, or less than 30%.
- cells in the polymer foam that are not open are closed cells.
- the density of the polymer foam sheet is less than 0.50 g/cc, less than 0.25 g/cc or less than 0.20 g/cc.
- the polymer foam sheet has a density of between 0.15 and 0.20 and an open cell content of between 30% and 40%.
- Example 1 Polypropylene Foams and Corresponding Density and Open Cell Content
- a polypropylene homopolymer with an MWD of 6 was foamed.
- Three polypropylene compositions were formed using a polypropylene homopolymer; the melt flow ratios, MWD, metallic acrylate salt composition, and additives of the polypropylene composition are listed in Table 1.
- the three polypropylene compositions were then foamed with CO2. The corresponding densities and open cell content percentages were measured and are listed in Table 2.
- MFR was measured using ASTM-D-1238. MWD was measured using GPC. Metallic acrylate salt and additive composition percentages are by weight.
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Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2017509608A JP2017514976A (en) | 2014-05-02 | 2015-04-29 | Polymer foam |
CA2948146A CA2948146A1 (en) | 2014-05-02 | 2015-04-29 | Polymer foams |
KR1020167030403A KR20170004979A (en) | 2014-05-02 | 2015-04-29 | Polymer foams |
EP15786224.4A EP3137247A4 (en) | 2014-05-02 | 2015-04-29 | Polymer foams |
CN201580021986.3A CN106232271A (en) | 2014-05-02 | 2015-04-29 | Foam of polymers |
MX2016014441A MX2016014441A (en) | 2014-05-02 | 2015-04-29 | Polymer foams. |
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US14/268,826 | 2014-05-02 | ||
US14/268,826 US20150315349A1 (en) | 2014-05-02 | 2014-05-02 | Polymer foams |
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WO2015168328A1 true WO2015168328A1 (en) | 2015-11-05 |
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PCT/US2015/028359 WO2015168328A1 (en) | 2014-05-02 | 2015-04-29 | Polymer foams |
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US (1) | US20150315349A1 (en) |
EP (1) | EP3137247A4 (en) |
JP (1) | JP2017514976A (en) |
KR (1) | KR20170004979A (en) |
CN (1) | CN106232271A (en) |
CA (1) | CA2948146A1 (en) |
MX (1) | MX2016014441A (en) |
WO (1) | WO2015168328A1 (en) |
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US10391363B2 (en) | 2017-02-16 | 2019-08-27 | Acushnet Company | Golf balls having a foam layer of a cross-linked thermoplastic composition |
CN110431175B (en) * | 2017-03-31 | 2022-12-16 | 索尔维特殊聚合物美国有限责任公司 | Foam material comprising polyphenylene sulfide polymer (PPS) |
CN107284217A (en) * | 2017-06-26 | 2017-10-24 | 株洲时代新材料科技股份有限公司 | Light weight method of electric motor coach battery protection cover and products thereof |
WO2019086951A1 (en) * | 2017-11-05 | 2019-05-09 | Braskem, S.A. | Foam composition with improved properties and applications thereof |
EP4127060B1 (en) | 2020-03-26 | 2024-05-01 | Fina Technology, Inc. | High melt strength polypropylene and process of preparation thereof |
TWI736337B (en) * | 2020-06-24 | 2021-08-11 | 三晃股份有限公司 | Highly dispersible acrylic metal salt composition, its preparation method and resin composition containing it |
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Also Published As
Publication number | Publication date |
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JP2017514976A (en) | 2017-06-08 |
EP3137247A1 (en) | 2017-03-08 |
KR20170004979A (en) | 2017-01-11 |
CN106232271A (en) | 2016-12-14 |
EP3137247A4 (en) | 2017-11-01 |
US20150315349A1 (en) | 2015-11-05 |
MX2016014441A (en) | 2017-02-23 |
CA2948146A1 (en) | 2015-11-05 |
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