WO2018028111A1 - Foam pad and preparation method therefor - Google Patents

Foam pad and preparation method therefor Download PDF

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Publication number
WO2018028111A1
WO2018028111A1 PCT/CN2016/111474 CN2016111474W WO2018028111A1 WO 2018028111 A1 WO2018028111 A1 WO 2018028111A1 CN 2016111474 W CN2016111474 W CN 2016111474W WO 2018028111 A1 WO2018028111 A1 WO 2018028111A1
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WO
WIPO (PCT)
Prior art keywords
base layer
screw extruder
foaming
film
extrusion
Prior art date
Application number
PCT/CN2016/111474
Other languages
French (fr)
Chinese (zh)
Inventor
王衍萍
Original Assignee
江苏锦厚新材料科技有限公司
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Filing date
Publication date
Application filed by 江苏锦厚新材料科技有限公司 filed Critical 江苏锦厚新材料科技有限公司
Priority to DE112016000112.6T priority Critical patent/DE112016000112T5/en
Publication of WO2018028111A1 publication Critical patent/WO2018028111A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/18Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
    • 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
    • C08L23/06Polyethene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • B29C44/04Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles consisting of at least two parts of chemically or physically different materials, e.g. having different densities
    • B29C44/06Making multilayered articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/20Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of indefinite length
    • B29C44/22Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of indefinite length consisting of at least two parts of chemically or physically different materials, e.g. having different densities
    • B29C44/24Making multilayered articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/46Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
    • B29C44/50Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
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    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/065Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
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    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • 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
    • B65D41/00Caps, e.g. crown caps or crown seals, i.e. members having parts arranged for engagement with the external periphery of a neck or wall defining a pouring opening or discharge aperture; Protective cap-like covers for closure members, e.g. decorative covers of metal foil or paper
    • B65D41/02Caps or cap-like covers without lines of weakness, tearing strips, tags, or like opening or removal devices
    • B65D41/04Threaded or like caps or cap-like covers secured by rotation
    • B65D41/0435Threaded or like caps or cap-like covers secured by rotation with separate sealing elements
    • 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
    • C08L23/12Polypropene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/46Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
    • B29C44/50Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying
    • B29C44/505Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying extruding the compound through a flat die
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/26Sealing devices, e.g. packaging for pistons or pipe joints
    • B29L2031/265Packings, Gaskets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/24All layers being polymeric
    • B32B2250/242All polymers belonging to those covered by group B32B27/32
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/40Symmetrical or sandwich layers, e.g. ABA, ABCBA, ABCCBA
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/02Organic
    • B32B2266/0207Materials belonging to B32B25/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/02Organic
    • B32B2266/0214Materials belonging to B32B27/00
    • B32B2266/025Polyolefin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/10Composition of foam characterised by the foam pores
    • B32B2266/102Nanopores, i.e. with average diameter smaller than 0.1 µm
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/10Composition of foam characterised by the foam pores
    • B32B2266/104Micropores, i.e. with average diameter in the range from 0.1 µm to 0.1 mm
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/10Composition of foam characterised by the foam pores
    • B32B2266/106Unimodal pore distribution
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/546Flexural strength; Flexion stiffness
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/72Density
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/732Dimensional properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2435/00Closures, end caps, stoppers
    • B32B2435/02Closures, end caps, stoppers for containers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/14Applications used for foams
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/16Applications used for films
    • 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
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

Definitions

  • the invention belongs to the technical field of high safety fields such as food packaging and pharmaceutical packaging, and relates to a foaming pad and a preparation method thereof, in particular to a sealing gasket for a bottle cap and a preparation method thereof.
  • the cap gasket is a material that uses rubber, copper or paper to be placed between the two planes to enhance the seal and to prevent fluid leakage. With the continuous development of the economy, cap gaskets are widely used in the wine, food, cosmetics, pharmaceutical and other industries.
  • the gaskets used in food packaging are PVC (polyvinyl chloride), PE (polyethylene), rubber backing pad, aluminum foil composite gasket, paper-plastic aluminum composite gasket, etc., among which PVC and PE are the main materials. .
  • CN 104250404A discloses a can cap gasket granule and a preparation method thereof, the can cap gasket granules being formulated in mass parts, comprising 30-50 parts of polypropylene, 30-50 parts of polyethylene, thermoplastic 10-30 parts of the elastomer, 0.4-5 parts of the processing aid, the above raw materials are mixed by a high-mixer, extruded by an extruder, cooled, and diced to obtain canned bottle gasket pellets.
  • the canned cap gasket pellets are completely safe and non-toxic. It does not add plasticizers such as o-benzene which are harmful to the human body, which not only satisfies the need for safe and non-toxic pellets for food cans, but also has excellent sealing properties.
  • CN 1465507A discloses a bottle inner pad material and its use in a hot-filled beverage plastic bottle cap, modified EVA (ethylene-vinyl acetate copolymer), SEBS (hydrogenated styrene diene copolymer) by maleic acid ), a combination of hydrogenated paraffin oil, branched low density polyethylene, polypropylene, polystyrene and low molecular lubricant, containing EVA with a VA (vinyl acetate) content of 18%, weight ratio of 5-60%, added The ethylene- ⁇ -olefin copolymer has a weight ratio of 90-35%. This material is not found in conventional cover gasket materials.
  • the inner cushion material prepared by the blending has superior performance compared with the inner cushion material of the existing beverage packaging plastic bottle cap, and the gasket material is not only low in price, but also has a material than the traditional hot-filled plastic bottle cap inner pad material. The effect is good.
  • the object of the present invention is to provide a foaming pad and a preparation method thereof, which are soft, flexible and elastic, and are food-grade plastic sheets for cap gaskets. It has excellent sealing properties, and its preparation method is simple and convenient for industrial application.
  • One of the objects of the present invention is to provide a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and having uniform capillary pores
  • the average pore diameter of the capillary is 1-100 ⁇ m, such as 2 ⁇ m, 5 ⁇ m, 8 ⁇ m, 10 ⁇ m, 12 ⁇ m, 15 ⁇ m, 18 ⁇ m, 20 ⁇ m, 30 ⁇ m, 40 ⁇ m, 50 ⁇ m, 60 ⁇ m, 80 ⁇ m, 90 ⁇ m or 95 ⁇ m, etc.;
  • the layer is even and dense;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • PE polyethylene 0-90%, such as 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 85%;
  • PP polypropylene 0-90%, such as 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 85%;
  • POE ethylene-octene copolymer
  • SBS block copolymer of styrene and butadiene
  • SEBS hydrogenated styrene-butadiene block copolymer
  • the release agent is 0.2-1.0%, such as 0.3%, 0.5%, 0.6%, 0.7%, 0.8% or 0.9%;
  • Nucleating agent 0.1-2.5% such as 0.3%, 0.5%, 0.8%, 1.0%, 1.2%, 1.5%, 1.8%, 2.0% or 2.3%;
  • the mass percentage of at most one of PE and PP is 0; the combination of POE, SBS or SEBS, such as POE and SBS, POE and SEBS, POE, SBS and SEBS.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • PE 0-93% such as 2%, 3%, 5%, 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90%;
  • PP 0-95% such as 1%, 3%, 5%, 8%, 10%, 20%, 30%, 50%, 60%, 80% or 90%;
  • POE 0-93% such as 2%, 3%, 5%, 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90%;
  • Tackifier 0-30%, such as 1%, 3%, 5%, 8%, 10%, 12%, 15%, 18%, 20%, 23%, 25% or 28%, etc.;
  • the release agent is 0.2-1.1%, such as 0.3%, 0.5%, 0.8% or 1.0%;
  • the opening agent is 0.1-3.0%, such as 0.3%, 0.5%, 0.8%, 1.0%, 1.2%, 1.5%, 1.8%, 2.0%, 2.1%, 2.3%, 2.5% or 2.8%;
  • the mass percentage of at most one of PE, PP and POE is zero.
  • the fact that the base layer is a uniform capillary pore means that the base layer contains a plurality of uniformly distributed capillary pores.
  • the base layer is prepared by massing the following materials:
  • the release agent is selected from any one or a combination of at least two of a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide, which is a carrier of PE or PP.
  • a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide which is a carrier of PE or PP.
  • a typical but non-limiting combination such as a combination of oleic acid amide and erucamide, a combination of oleic acid amide and oleic acid amide with a erucamide amide or a masterbatch based on PE or PP, erucamide and oleic acid amide
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials by mass percentage:
  • the tackifier is selected from any one or a combination of at least two of EEA (ethylene ethyl acrylate), polyester or maleic anhydride graft resin.
  • EEA ethylene ethyl acrylate
  • Typical but non-limiting combinations are combinations of EEA and polyester, combinations of EEA with maleic anhydride grafted resins, combinations of EEA, polyester and maleic anhydride grafted resins.
  • the release agent is selected from any one or a combination of at least two of a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide, which is a carrier of PE or PP.
  • a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide which is a carrier of PE or PP.
  • a typical but non-limiting combination such as a combination of oleic acid amide and erucamide, a combination of oleic acid amide and oleic acid amide with a erucamide amide or a masterbatch based on PE or PP, erucamide and oleic acid amide
  • the opening agent is selected from the group consisting of erucamide.
  • the base layer has a thickness of 0.5 to 10.0 mm, such as 0.8 mm, 1.0 mm, 1.5 mm, 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm, 8.0 mm, or 9.0 mm. If it is too thick, the application performance such as material sealing performance is not guaranteed; if it is too thin, the flexibility of the material and the compensation performance are insufficient.
  • the base layer has a density of 100-800 kg/m 3 , such as 150 kg/m 3 , 200 kg/m 3 , 300 kg/m 3 , 400 kg/m 3 , 500 kg/m 3 , 600 kg/m 3 or 700 kg/ m 3 and so on.
  • the base layer is excellent in cross-linking sealing property due to supercritical physical foaming.
  • the film layer has a thickness of from 0.02 to 0.15 mm, such as 0.05 mm, 0.08 mm, 0.10 mm, 0.12 mm or 0.14 mm, and the like. If the film is too thick, the flexibility of the material will not be sufficient to compensate for the performance. If the film is too thin, the application performance such as material sealing performance is not guaranteed.
  • the thickness of the film layer is 0.02-0.15 mm means The thickness of the upper surface film layer of the base layer and the thickness of the lower surface film layer are independently 0.02 to 0.15 mm.
  • the film layer allows the foam pad to have good flexibility and meet the sealing functional requirements.
  • Another object of the present invention is to provide a method for preparing a foaming mat as described above, which comprises the following steps:
  • the formulated amount of the film raw material is fed into a single-screw extruder hopper, and a film is deposited on the surface of the base layer to obtain the foamed mat.
  • the single-screw extruder of the step (1) is a single-screw extruder having heating and cooling withstand characteristics, and a typical but non-limiting single-screw extruder such as a foaming machine manufactured by Berstorff Co., Ltd.: 150 -ISO-PAC.
  • the host temperature of the single-screw extruder is ⁇ 65 ° C, such as 63 ° C, 60 ° C, 58 ° C, 55 ° C, 50 ° C, 45 ° C or 30 ° C, etc., the host temperature is too high, This will result in damage to the unit.
  • the extrusion temperature in the step (1) is 90-210 ° C, such as 100 ° C, 110 ° C, 130 ° C, 150 ° C, 180 ° C, 190 ° C or 200 ° C, etc., and the extrusion temperature is high, then the film formability Poor, uneven thickness, uneven foaming; low extrusion temperature, film foaming uneven or unable to foam.
  • the rotation speed of the screw during the extrusion in the step (1) is 1-100 rpm, such as 2 rpm, 3 rpm, 5 rpm, 10 rpm, 20 rpm, 30 rpm, 40 rpm, 50 rpm, 60 rpm, 70 rpm, 80 rpm or 90 rpm, and the like.
  • the single screw extruder of step (1) has a pressure range of 0-250 bar, such as 2 bar, 5 bar, 10 bar, 20 bar, 50 bar, 100 bar, 120 bar, 150 bar, 180 bar, 200 bar, 220 bar or 240 bar, and the like.
  • the flow rate of the supercritical carbon dioxide in the step (1) is 0.10-2.50 kg/h, such as 0.3 kg/h, 0.5 kg/h, 0.8 kg/h, 1.0 kg/h, 1.2 kg/h, 1.5 kg/h, 1.8kg / h, 2.0kg / h or 2.3kg / h, etc., the flow rate of carbon dioxide is high, the film foaming is uneven, excessive foaming, material elasticity failure; low flow, foaming is too low, flexibility is not enough.
  • the thickness of the base layer in the step (1) is 0.5-10.0 mm, such as 0.8 mm, 1.0 mm, 1.5 mm, 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm, 8.0 mm or 9.0 mm, etc. .
  • the density of the base layer in the step (1) is 100-800 kg/m 3 , such as 150 kg/m 3 , 200 kg/m 3 , 300 kg/m 3 , 400 kg/m 3 , 500 kg/m 3 , 600 kg/m. 3 or 700kg/m 3 and so on.
  • the temperature of the extrusion in the step (2) is 80-250 ° C, such as 85 ° C, 90 ° C, 95 ° C, 100 ° C, 120 ° C, 130 ° C, 150 ° C, 180 ° C, 200 ° C, 210 ° C, 220 ° C or 240 ° C and so on.
  • the rotation speed of the screw during the extrusion in the step (2) is 1-100 rpm, such as 2 rpm, 3 rpm, 5 rpm, 10 rpm, 20 rpm, 30 rpm, 40 rpm, 50 rpm, 60 rpm, 70 rpm, 80 rpm or 90 rpm, and the like.
  • the thickness of the base layer coating in the step (2) is 0.02-0.15 mm, such as 0.05 mm, 0.08 mm, 0.10 mm, 0.12 mm or 0.14 mm.
  • the coating in step (2) can be made into a functional film according to the needs of downstream applications.
  • the preparation method comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 50-220 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 0.10-2.50. Kg/h, after extrusion, to obtain a substrate layer having a density of 100-800 kg/m 3 and a thickness of 0.5-10.0 mm, wherein the main screw temperature of the single-screw extruder during the extrusion process is ⁇ 65 ° C; The temperature is 90-210 ° C; the speed of the screw during extrusion is 1-100 rpm; the pressure range of the single-screw extruder is 0-250 bar;
  • the film material of the formula amount is sent into the hopper of the single-screw extruder, and the film is coated on the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.02-0.15 mm, wherein the extrusion temperature is 80- 250 ° C; the speed of the screw during extrusion is 1-100 rpm.
  • the foaming mat provided by the invention comprises a base layer and a film layer, the base layer is obtained by foaming, has good cross-linking sealing property, and has better flexibility, flexibility and elasticity, and the surface covered film layer makes the The foaming pad has good flexibility and meets the sealing functional requirements. Its Shore A hardness is 35-50. It has excellent sealing property and good opening performance for the cap gasket. And the effect of improving the flatness, in addition, it is a food grade plastic sheet;
  • the foaming mat provided by the invention has a simple preparation method and is convenient for industrial application.
  • the single-screw extruder of the step (1) is a single-screw extruder having heating, cooling and pressure resistance characteristics - a foaming machine manufactured by Berstorff Co., Ltd.: 150- ISO-PAC.
  • the thickness of the film layer described in the following examples is a numerical value means that the thickness of the upper surface film layer of the base layer and the thickness of the lower surface film layer are independently a certain value.
  • a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 1 to 30 ⁇ m; the film layer is uniform and dense; the thickness of the substrate layer is 0.5 mm; The thickness is 0.02 mm;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the release agent is selected from the group consisting of oleic acid amide;
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the tackifier is selected from the group consisting of EEA (ethylene acrylate).
  • the release agent is selected from oleic acid amides.
  • the opening agent is selected from the group consisting of erucamide.
  • the preparation method of the foaming pad comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 50 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.50 kg/h.
  • a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 65 ° C; an extrusion temperature of 210 ° C; and a screw rotation speed of 1 rpm during extrusion;
  • the screw extruder has a pressure range of 250 bar;
  • a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film layer of 50-100 ⁇ m; the film layer is uniform and dense; the thickness of the substrate layer is 10.0 mm; the thickness of the film layer is 0.15 mm;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the release agent is selected from the group consisting of oleic acid amides and erucamides.
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the tackifier is selected from the group consisting of EEA and polyester.
  • the release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
  • the opening agent is selected from the group consisting of erucamide.
  • the preparation method of the foaming pad comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 220 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 0.10 kg/h.
  • a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 50 ° C; an extrusion temperature of 90 ° C; and a screw rotation speed of 100 rpm during extrusion;
  • the screw extruder has a pressure range of 100 bar;
  • a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 30-80 ⁇ m; the film layer is uniform and dense; the thickness of the substrate layer is 5.0 mm; the thickness of the film layer is 0.10 mm;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the release agent is selected from the group consisting of erucamide.
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the tackifier is selected from the group consisting of maleic anhydride graft resins.
  • the release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
  • the opening agent is selected from the group consisting of erucamide.
  • the preparation method of the foaming pad comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 100 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 1.00 kg/h.
  • a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 60 ° C; an extrusion temperature of 120 ° C; and a screw rotation speed of 20 rpm during extrusion;
  • the screw extruder has a pressure range of 120 bar;
  • a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores
  • the film layer is a laminating layer, the film layer is uniform and dense; the thickness of the substrate layer is 3.0 mm; the thickness of the film layer is 0.05 mm;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the tackifier is selected from the group consisting of EEA, polyester and maleic anhydride graft resin in terms of mass ratio A 1:1:1 combination.
  • the release agent is selected from oleic acid amides.
  • the opening agent is selected from the group consisting of erucamide.
  • the preparation method of the foaming pad comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 150 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.0 kg/h.
  • a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 55 ° C; an extrusion temperature of 170 ° C; and a screw rotation speed of 80 rpm during extrusion;
  • the screw extruder has a pressure range of 150 bar;
  • a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 1-100 ⁇ m; the film layer is uniform and dense; the thickness of the substrate layer is 3.0 mm; the thickness of the film layer is 0.05 mm;
  • the base layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the release agent is selected from oleic acid amides.
  • the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
  • the film layer is mainly prepared from the following raw materials in terms of mass percentage:
  • the tackifier is selected from the group consisting of maleic anhydride graft resins.
  • the release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
  • the opening agent is selected from the group consisting of erucamide.
  • the preparation method of the foaming pad comprises the following steps:
  • the formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 150 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.0 kg/h.
  • a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 55 ° C; an extrusion temperature of 170 ° C; and a screw rotation speed of 80 rpm during extrusion;
  • the screw extruder has a pressure range of 150 bar;
  • the comparative example 1 is the base layer obtained in Example 3.
  • the comparative example 2 is a commercially available PE gasket (manufacturer: Shanghai Mingyuan Plastic Products Co., Ltd.).
  • a foaming pad and a preparation method thereof are the same as those in Embodiment 5 except that the flow rate of supercritical carbon dioxide is 0.08 kg/h.
  • a foaming pad and a preparation method thereof are the same as in the embodiment 5 except that the flow rate of the supercritical carbon dioxide is 2.60 kg/h.
  • the products obtained in Examples 1-5 and Comparative Examples 1-4 were tested for performance.
  • the density test method was GB1033
  • the flexibility test method was the inductive test
  • the Shore hardness test method was GB2411
  • the seal test method was Self-made oil-infiltration method (the bottle cap made of foaming pad is sealed with glass bottle filled with edible oil, placed on the platform with white paper on the side, and after 10 days, it is observed whether there is oil leakage on the white paper, the oil seepage is unqualified, no The oil seepage is acceptable).
  • the test results are shown in Table 1 below:
  • Comparative example 1 305g/L general 57 qualified Comparative example 2 297g/L general 60 qualified Comparative example 3 412g/L general 65 qualified Comparative example 4 263g/L general 62 qualified
  • the foaming pad provided by the invention has excellent performance and excellent sealing performance for the cap gasket.
  • the foaming pad provided by the invention meets food grade requirements and can be widely used in high security fields such as food packaging and pharmaceutical packaging.

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  • Chemical Kinetics & Catalysis (AREA)
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  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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  • Sealing Material Composition (AREA)
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  • Closures For Containers (AREA)

Abstract

Provided are a foam pad and a preparation method therefor. The foam pad comprises a base layer and film layers covering the upper surface and the lower surface of the base layer. The base layer is a foam body and is a uniform porous body, wherein the average pore size of the pores is 1-100 μm. The film layers are uniform and dense. The preparation method for the foam pad comprises a supercritical foaming process and a filming process. The foam pad has good flexibility, softness and elasticity, is a food-grade plastic sheet, and has good tightness when being used for a bottle cap gasket. The preparation method is simple and can be easily industrialized.

Description

一种发泡垫及其制备方法Foaming pad and preparation method thereof 技术领域Technical field
本发明属于食品包装、药品包装等高安全领域技术领域,涉及一种发泡垫及其制备方法,尤其涉及一种瓶盖上用的密封垫片及其制备方法。The invention belongs to the technical field of high safety fields such as food packaging and pharmaceutical packaging, and relates to a foaming pad and a preparation method thereof, in particular to a sealing gasket for a bottle cap and a preparation method thereof.
背景技术Background technique
瓶盖垫片是使用橡胶皮、铜片或纸张,用来放到两平面之间用以加强密封的材料,具有防止流体泄漏的作用。随着经济的不断发展,瓶盖垫片被广泛应用在酒类、食品、化妆品、药品等行业中。The cap gasket is a material that uses rubber, copper or paper to be placed between the two planes to enhance the seal and to prevent fluid leakage. With the continuous development of the economy, cap gaskets are widely used in the wine, food, cosmetics, pharmaceutical and other industries.
据相关新闻报道,目前我国酒类包装和饮料类包装对瓶盖垫片的需求日益增大,而酒类包装使用的瓶盖垫片占瓶盖垫片使用总量的70%以上。随着我国酒类和饮料行业的快速发展,瓶盖垫片行业逐渐崛起。2014年我国瓶盖垫片的生产总量相较2013年同比上涨14%,这种巨大的需求不仅拉动瓶盖垫片价格一路上升,还使瓶盖垫片生产厂家的数量快速增加。目前,我国已成为全世界最大的瓶盖垫片消费国和出口国。According to relevant news reports, the demand for cap gaskets in China's wine packaging and beverage packaging is increasing, and the cap gaskets used in alcohol packaging account for more than 70% of the total use of cap gaskets. With the rapid development of China's wine and beverage industry, the cap gasket industry has gradually emerged. In 2014, the total production of cap gaskets in China increased by 14% compared with 2013. This huge demand not only drove the price of cap gaskets, but also increased the number of cap gasket manufacturers. At present, China has become the world's largest consumer and exporter of cap gaskets.
我国瓶盖垫片市场的产品多达几百种,各种型号规格和类型的瓶盖垫片充斥着食品包装容器市场。目前,运用在食品包装中的垫片有PVC(聚氯乙烯)、PE(聚乙烯)、回力胶垫、铝箔复合垫片、纸塑铝复合垫片等材质,其中以PVC、PE材质为主。There are hundreds of products in the cap gasket market in China, and various types of specifications and types of cap gaskets are filled with the food packaging container market. At present, the gaskets used in food packaging are PVC (polyvinyl chloride), PE (polyethylene), rubber backing pad, aluminum foil composite gasket, paper-plastic aluminum composite gasket, etc., among which PVC and PE are the main materials. .
CN 104250404A公开了一种罐头瓶盖垫片粒料及其制备方法,所述罐头瓶盖垫片粒料其配方按质量份数计,包括聚丙烯30-50份、聚乙烯30-50份、热塑性弹性体10-30份,加工助剂0.4-5份,上述原料经高混机混合、挤出机挤出、冷却、切粒得罐头瓶盖垫片粒料。该罐头瓶盖垫片粒料完全采用安全无毒的原 料,不添加对人体有害的邻苯类等增塑剂,既满足了食品罐头包装用瓶盖垫片粒料安全无毒的需求又具有优良的密封性。CN 104250404A discloses a can cap gasket granule and a preparation method thereof, the can cap gasket granules being formulated in mass parts, comprising 30-50 parts of polypropylene, 30-50 parts of polyethylene, thermoplastic 10-30 parts of the elastomer, 0.4-5 parts of the processing aid, the above raw materials are mixed by a high-mixer, extruded by an extruder, cooled, and diced to obtain canned bottle gasket pellets. The canned cap gasket pellets are completely safe and non-toxic. It does not add plasticizers such as o-benzene which are harmful to the human body, which not only satisfies the need for safe and non-toxic pellets for food cans, but also has excellent sealing properties.
CN 1465507A公开了一种瓶盖内垫材料及其在热灌装饮料塑料瓶盖上的应用,通过马来酸改性EVA(乙烯-醋酸乙烯共聚物)、SEBS(氢化苯乙烯二烯烃共聚物)、氢化石蜡油、分支状低密度聚乙烯、聚丙烯、聚苯乙烯和低分子润滑剂的组合构成,含有VA(醋酸乙烯)含量为18%的EVA,重量比为5-60%,加入乙烯-α烯烃共聚物,重量比为90-35%。该材料是传统的盖衬垫材料中所没有的。这种共混制得的内垫材料与现有饮料包装塑料瓶盖内垫材料相比,具有优良的性能,垫片材料不但价格低廉,而且比传统热灌装饮塑料瓶盖内垫材料的效果好。CN 1465507A discloses a bottle inner pad material and its use in a hot-filled beverage plastic bottle cap, modified EVA (ethylene-vinyl acetate copolymer), SEBS (hydrogenated styrene diene copolymer) by maleic acid ), a combination of hydrogenated paraffin oil, branched low density polyethylene, polypropylene, polystyrene and low molecular lubricant, containing EVA with a VA (vinyl acetate) content of 18%, weight ratio of 5-60%, added The ethylene-α-olefin copolymer has a weight ratio of 90-35%. This material is not found in conventional cover gasket materials. The inner cushion material prepared by the blending has superior performance compared with the inner cushion material of the existing beverage packaging plastic bottle cap, and the gasket material is not only low in price, but also has a material than the traditional hot-filled plastic bottle cap inner pad material. The effect is good.
但是,现有的瓶盖垫片,其密封性还有待进一步提高。However, the sealing properties of the existing cap gaskets have yet to be further improved.
发明内容Summary of the invention
针对现有技术存在的不足,本发明的目的在于提供一种发泡垫及其制备方法,所述发泡垫柔韧性、柔软性及弹性好,为食品级塑料片,用于瓶盖垫片具有优异的密封性,并且其制备方法简单,便于工业化应用。In view of the deficiencies of the prior art, the object of the present invention is to provide a foaming pad and a preparation method thereof, which are soft, flexible and elastic, and are food-grade plastic sheets for cap gaskets. It has excellent sealing properties, and its preparation method is simple and convenient for industrial application.
1bar=0.1MPa。1 bar = 0.1 MPa.
为达此目的,本发明采用以下技术方案:To this end, the present invention employs the following technical solutions:
本发明的目的之一在于提供一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,所述毛细孔的平均孔径为1-100μm,如2μm、5μm、8μm、10μm、12μm、15μm、18μm、20μm、30μm、40μm、50μm、60μm、80μm、90μm或95μm等;所述膜层均匀致密;One of the objects of the present invention is to provide a foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and having uniform capillary pores The average pore diameter of the capillary is 1-100 μm, such as 2 μm, 5 μm, 8 μm, 10 μm, 12 μm, 15 μm, 18 μm, 20 μm, 30 μm, 40 μm, 50 μm, 60 μm, 80 μm, 90 μm or 95 μm, etc.; The layer is even and dense;
所述基体层按质量百分含量主要由如下原料制备得到: The base layer is mainly prepared from the following raw materials in terms of mass percentage:
PE(聚乙烯)0-90%,如2%、5%、10%、20%、30%、40%、50%、60%、70%、80%或85%等;PE (polyethylene) 0-90%, such as 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 85%;
PP(聚丙烯)0-90%,如2%、5%、10%、20%、30%、40%、50%、60%、70%、80%或85%等;PP (polypropylene) 0-90%, such as 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 85%;
POE(乙烯-辛烯共聚物)、SBS(苯乙烯与丁二烯的嵌段共聚物)或SEBS(氢化苯乙烯-丁二烯嵌段共聚物)中的任意一种或至少两种的组合0-20%(不包含0),如0.5%、1%、2%、3%、5%、6%、8%、10%、12%、15%或18%等;Any one or a combination of at least two of POE (ethylene-octene copolymer), SBS (block copolymer of styrene and butadiene) or SEBS (hydrogenated styrene-butadiene block copolymer) 0-20% (excluding 0), such as 0.5%, 1%, 2%, 3%, 5%, 6%, 8%, 10%, 12%, 15% or 18%;
脱模剂0.2-1.0%,如0.3%、0.5%、0.6%、0.7%、0.8%或0.9%等;The release agent is 0.2-1.0%, such as 0.3%, 0.5%, 0.6%, 0.7%, 0.8% or 0.9%;
成核剂0.1-2.5%,如0.3%、0.5%、0.8%、1.0%、1.2%、1.5%、1.8%、2.0%或2.3%等;Nucleating agent 0.1-2.5%, such as 0.3%, 0.5%, 0.8%, 1.0%, 1.2%, 1.5%, 1.8%, 2.0% or 2.3%;
色母0-2.0%,如0.1%、0.5%、0.8%、1.0%、1.2%、1.3%、1.5%、1.7%或1.9%等;Color masterbatch 0-2.0%, such as 0.1%, 0.5%, 0.8%, 1.0%, 1.2%, 1.3%, 1.5%, 1.7% or 1.9%;
其中,PE和PP中至多一种物质的质量百分含量为0;POE、SBS或SEBS的组合如,POE与SBS的组合,POE与SEBS的组合,POE、SBS与SEBS的组合。Wherein, the mass percentage of at most one of PE and PP is 0; the combination of POE, SBS or SEBS, such as POE and SBS, POE and SEBS, POE, SBS and SEBS.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
PE 0-93%,如2%、3%、5%、10%、20%、30%、50%、60%、70%、80%或90%等;PE 0-93%, such as 2%, 3%, 5%, 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90%;
PP 0-95%,如1%、3%、5%、8%、10%、20%、30%、50%、60%、80%或90%等;PP 0-95%, such as 1%, 3%, 5%, 8%, 10%, 20%, 30%, 50%, 60%, 80% or 90%;
POE 0-93%,如2%、3%、5%、10%、20%、30%、50%、60%、70%、80%或90%等;POE 0-93%, such as 2%, 3%, 5%, 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90%;
增粘剂0-30%,如1%、3%、5%、8%、10%、12%、15%、18%、20%、 23%、25%或28%等;Tackifier 0-30%, such as 1%, 3%, 5%, 8%, 10%, 12%, 15%, 18%, 20%, 23%, 25% or 28%, etc.;
脱模剂0.2-1.1%,如0.3%、0.5%、0.8%或1.0%等;The release agent is 0.2-1.1%, such as 0.3%, 0.5%, 0.8% or 1.0%;
开口剂0.1-3.0%,如0.3%、0.5%、0.8%、1.0%、1.2%、1.5%、1.8%、2.0%、2.1%、2.3%、2.5%或2.8%等;The opening agent is 0.1-3.0%, such as 0.3%, 0.5%, 0.8%, 1.0%, 1.2%, 1.5%, 1.8%, 2.0%, 2.1%, 2.3%, 2.5% or 2.8%;
其中,PE、PP和POE中至多一种物质的质量百分含量为0。Among them, the mass percentage of at most one of PE, PP and POE is zero.
所述基体层为均匀的毛细孔状体是指所述基体层包含多个均匀分布的毛细孔。The fact that the base layer is a uniform capillary pore means that the base layer contains a plurality of uniformly distributed capillary pores.
作为优选的技术方案,所述基体层按质量百分含量由如下原料制备得到:As a preferred technical solution, the base layer is prepared by massing the following materials:
Figure PCTCN2016111474-appb-000001
Figure PCTCN2016111474-appb-000001
优选地,所述脱模剂选自油酸酰胺、芥酸酰胺或油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料中的任意一种或至少两种的组合。典型但非限制性的组合如油酸酰胺与芥酸酰胺的组合,油酸酰胺和油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料的组合,芥酸酰胺和油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料的组合。Preferably, the release agent is selected from any one or a combination of at least two of a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide, which is a carrier of PE or PP. A typical but non-limiting combination such as a combination of oleic acid amide and erucamide, a combination of oleic acid amide and oleic acid amide with a erucamide amide or a masterbatch based on PE or PP, erucamide and oleic acid amide A combination of a masterbatch made of erucamide or a carrier based on PE or PP.
优选地,所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。Preferably, the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
作为优选的技术方案,所述膜层按质量百分含量主要由如下原料制备得到:As a preferred technical solution, the film layer is mainly prepared from the following raw materials by mass percentage:
Figure PCTCN2016111474-appb-000002
Figure PCTCN2016111474-appb-000002
Figure PCTCN2016111474-appb-000003
Figure PCTCN2016111474-appb-000003
优选地,所述增粘剂选自EEA(乙烯丙烯酸乙酯)、聚酯或马来酸酐接枝树脂中的任意一种或至少两种的组合。典型但非限制性的组合如EEA与聚酯的组合,EEA与马来酸酐接枝树脂的组合,EEA、聚酯与马来酸酐接枝树脂的组合。Preferably, the tackifier is selected from any one or a combination of at least two of EEA (ethylene ethyl acrylate), polyester or maleic anhydride graft resin. Typical but non-limiting combinations are combinations of EEA and polyester, combinations of EEA with maleic anhydride grafted resins, combinations of EEA, polyester and maleic anhydride grafted resins.
优选地,所述脱模剂选自油酸酰胺、芥酸酰胺或油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料中的任意一种或至少两种的组合。典型但非限制性的组合如油酸酰胺与芥酸酰胺的组合,油酸酰胺和油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料的组合,芥酸酰胺和油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料的组合。Preferably, the release agent is selected from any one or a combination of at least two of a masterbatch made of oleic acid amide, erucic acid amide or oleic acid amide and erucic acid amide, which is a carrier of PE or PP. A typical but non-limiting combination such as a combination of oleic acid amide and erucamide, a combination of oleic acid amide and oleic acid amide with a erucamide amide or a masterbatch based on PE or PP, erucamide and oleic acid amide A combination of a masterbatch made of erucamide or a carrier based on PE or PP.
优选地,所述开口剂选自芥酸酰胺。Preferably, the opening agent is selected from the group consisting of erucamide.
所述基体层的厚度为0.5-10.0mm,如0.8mm、1.0mm、1.5mm、2.0mm、3.0mm、4.0mm、5.0mm、6.0mm、8.0mm或9.0mm等。过厚,则材料密封性能等应用性能没有保障;过薄,则材料的柔韧性,配合弥补性能不够。The base layer has a thickness of 0.5 to 10.0 mm, such as 0.8 mm, 1.0 mm, 1.5 mm, 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm, 8.0 mm, or 9.0 mm. If it is too thick, the application performance such as material sealing performance is not guaranteed; if it is too thin, the flexibility of the material and the compensation performance are insufficient.
优选地,所述基体层的密度为100-800kg/m3,如150kg/m3、200kg/m3、300kg/m3、400kg/m3、500kg/m3、600kg/m3或700kg/m3等。Preferably, the base layer has a density of 100-800 kg/m 3 , such as 150 kg/m 3 , 200 kg/m 3 , 300 kg/m 3 , 400 kg/m 3 , 500 kg/m 3 , 600 kg/m 3 or 700 kg/ m 3 and so on.
所述基体层由于经过超临界物理发泡,其交联密封性优异。The base layer is excellent in cross-linking sealing property due to supercritical physical foaming.
优选地,所述膜层的厚度为0.02-0.15mm,如0.05mm、0.08mm、0.10mm、0.12mm或0.14mm等。膜层过厚则材料的柔韧性,配合弥补性能不够,膜层过薄则材料密封性能等应用性能没有保障。所述膜层的厚度为0.02-0.15mm是指 基体层的上表面膜层的厚度和下表面膜层的厚度独立地为0.02-0.15mm。Preferably, the film layer has a thickness of from 0.02 to 0.15 mm, such as 0.05 mm, 0.08 mm, 0.10 mm, 0.12 mm or 0.14 mm, and the like. If the film is too thick, the flexibility of the material will not be sufficient to compensate for the performance. If the film is too thin, the application performance such as material sealing performance is not guaranteed. The thickness of the film layer is 0.02-0.15 mm means The thickness of the upper surface film layer of the base layer and the thickness of the lower surface film layer are independently 0.02 to 0.15 mm.
所述膜层使得所述发泡垫具备良好的柔韧匹配性的同时,也满足密封功能性要求。The film layer allows the foam pad to have good flexibility and meet the sealing functional requirements.
本发明的目的之二还在于提供一种如上所述的发泡垫的制备方法,所述制备方法包括如下步骤:Another object of the present invention is to provide a method for preparing a foaming mat as described above, which comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入超临界二氧化碳,经挤出发泡,得到基体层,所述超临界二氧化碳为50-220bar压力下的超临界二氧化碳,如60bar、80bar、90bar、100bar、120bar、150bar、180bar或200bar压力下的超临界二氧化碳;(1) feeding the formulated amount of the base layer raw material into the hopper of the single-screw extruder, simultaneously charging the central portion of the single-screw extruder with supercritical carbon dioxide, and extruding and foaming to obtain a base layer, the supercritical carbon dioxide Supercritical carbon dioxide at a pressure of 50-220 bar, such as supercritical carbon dioxide at a pressure of 60 bar, 80 bar, 90 bar, 100 bar, 120 bar, 150 bar, 180 bar or 200 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到所述发泡垫。(2) The formulated amount of the film raw material is fed into a single-screw extruder hopper, and a film is deposited on the surface of the base layer to obtain the foamed mat.
步骤(1)所述单螺杆挤出机为具有加热冷却耐压特性的单螺杆挤出机,典型但非限制性的单螺杆挤出机如贝尔斯托夫有限公司制造的发泡机:150-ISO-PAC。The single-screw extruder of the step (1) is a single-screw extruder having heating and cooling withstand characteristics, and a typical but non-limiting single-screw extruder such as a foaming machine manufactured by Berstorff Co., Ltd.: 150 -ISO-PAC.
步骤(1)所述挤出过程中单螺杆挤出机的主机温度≤65℃,如63℃、60℃、58℃、55℃、50℃、45℃或30℃等,主机温度过高,则导致机组损坏。In the extrusion process of the step (1), the host temperature of the single-screw extruder is ≤65 ° C, such as 63 ° C, 60 ° C, 58 ° C, 55 ° C, 50 ° C, 45 ° C or 30 ° C, etc., the host temperature is too high, This will result in damage to the unit.
优选地,步骤(1)所述挤出温度为90-210℃,如100℃、110℃、130℃、150℃、180℃、190℃或200℃等,挤出温度高,则膜成型性不良,厚薄不均,发泡不均匀;挤出温度低,则膜发泡不均或无法发泡。Preferably, the extrusion temperature in the step (1) is 90-210 ° C, such as 100 ° C, 110 ° C, 130 ° C, 150 ° C, 180 ° C, 190 ° C or 200 ° C, etc., and the extrusion temperature is high, then the film formability Poor, uneven thickness, uneven foaming; low extrusion temperature, film foaming uneven or unable to foam.
优选地,步骤(1)所述挤出过程中螺杆的转速为1-100rpm,如2rpm、3rpm、5rpm、10rpm、20rpm、30rpm、40rpm、50rpm、60rpm、70rpm、80rpm或90rpm等。Preferably, the rotation speed of the screw during the extrusion in the step (1) is 1-100 rpm, such as 2 rpm, 3 rpm, 5 rpm, 10 rpm, 20 rpm, 30 rpm, 40 rpm, 50 rpm, 60 rpm, 70 rpm, 80 rpm or 90 rpm, and the like.
优选地,步骤(1)所述单螺杆挤出机的承压范围为0-250bar,如2bar、5bar、 10bar、20bar、50bar、100bar、120bar、150bar、180bar、200bar、220bar或240bar等。Preferably, the single screw extruder of step (1) has a pressure range of 0-250 bar, such as 2 bar, 5 bar, 10 bar, 20 bar, 50 bar, 100 bar, 120 bar, 150 bar, 180 bar, 200 bar, 220 bar or 240 bar, and the like.
步骤(1)所述超临界二氧化碳的流量为0.10-2.50kg/h,如0.3kg/h、0.5kg/h、0.8kg/h、1.0kg/h、1.2kg/h、1.5kg/h、1.8kg/h、2.0kg/h或2.3kg/h等,二氧化碳的流量高,则膜发泡不均、发泡过度、材料弹性失效;流量低,则发泡过低,柔韧性不够。The flow rate of the supercritical carbon dioxide in the step (1) is 0.10-2.50 kg/h, such as 0.3 kg/h, 0.5 kg/h, 0.8 kg/h, 1.0 kg/h, 1.2 kg/h, 1.5 kg/h, 1.8kg / h, 2.0kg / h or 2.3kg / h, etc., the flow rate of carbon dioxide is high, the film foaming is uneven, excessive foaming, material elasticity failure; low flow, foaming is too low, flexibility is not enough.
优选地,步骤(1)所述基体层的厚度为0.5-10.0mm,如0.8mm、1.0mm、1.5mm、2.0mm、3.0mm、4.0mm、5.0mm、6.0mm、8.0mm或9.0mm等。Preferably, the thickness of the base layer in the step (1) is 0.5-10.0 mm, such as 0.8 mm, 1.0 mm, 1.5 mm, 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm, 8.0 mm or 9.0 mm, etc. .
优选地,步骤(1)所述基体层的密度为100-800kg/m3,如150kg/m3、200kg/m3、300kg/m3、400kg/m3、500kg/m3、600kg/m3或700kg/m3等。Preferably, the density of the base layer in the step (1) is 100-800 kg/m 3 , such as 150 kg/m 3 , 200 kg/m 3 , 300 kg/m 3 , 400 kg/m 3 , 500 kg/m 3 , 600 kg/m. 3 or 700kg/m 3 and so on.
步骤(2)所述挤出的温度为80-250℃,如85℃、90℃、95℃、100℃、120℃、130℃、150℃、180℃、200℃、210℃、220℃或240℃等。The temperature of the extrusion in the step (2) is 80-250 ° C, such as 85 ° C, 90 ° C, 95 ° C, 100 ° C, 120 ° C, 130 ° C, 150 ° C, 180 ° C, 200 ° C, 210 ° C, 220 ° C or 240 ° C and so on.
优选地,步骤(2)所述挤出过程中螺杆的转速为1-100rpm,如2rpm、3rpm、5rpm、10rpm、20rpm、30rpm、40rpm、50rpm、60rpm、70rpm、80rpm或90rpm等。Preferably, the rotation speed of the screw during the extrusion in the step (2) is 1-100 rpm, such as 2 rpm, 3 rpm, 5 rpm, 10 rpm, 20 rpm, 30 rpm, 40 rpm, 50 rpm, 60 rpm, 70 rpm, 80 rpm or 90 rpm, and the like.
步骤(2)所述基体层覆膜厚度为0.02-0.15mm,如0.05mm、0.08mm、0.10mm、0.12mm或0.14mm等。The thickness of the base layer coating in the step (2) is 0.02-0.15 mm, such as 0.05 mm, 0.08 mm, 0.10 mm, 0.12 mm or 0.14 mm.
步骤(2)中的淋膜可根据下游应用需求进行功能膜制作。The coating in step (2) can be made into a functional film according to the needs of downstream applications.
作为优选的技术方案,所述制备方法包括如下步骤:As a preferred technical solution, the preparation method comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入50-220bar压力下的超临界二氧化碳,超临界二氧化碳的流量为0.10-2.50kg/h,经挤出,得到密度为100-800kg/m3,厚度为0.5-10.0mm的基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度≤65℃;挤出温度为 90-210℃;挤出过程中螺杆的转速为1-100rpm;所述单螺杆挤出机的承压范围为0-250bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 50-220 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 0.10-2.50. Kg/h, after extrusion, to obtain a substrate layer having a density of 100-800 kg/m 3 and a thickness of 0.5-10.0 mm, wherein the main screw temperature of the single-screw extruder during the extrusion process is ≤65 ° C; The temperature is 90-210 ° C; the speed of the screw during extrusion is 1-100 rpm; the pressure range of the single-screw extruder is 0-250 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.02-0.15mm的发泡垫,其中,挤出的温度为80-250℃;挤出过程中螺杆的转速为1-100rpm。(2) The film material of the formula amount is sent into the hopper of the single-screw extruder, and the film is coated on the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.02-0.15 mm, wherein the extrusion temperature is 80- 250 ° C; the speed of the screw during extrusion is 1-100 rpm.
与现有技术相比,本发明的有益效果为:Compared with the prior art, the beneficial effects of the present invention are:
本发明提供的发泡垫由基体层和膜层组成,基体层经发泡制得,交联密封性较好,并且柔韧性、柔软性及弹性较好,其表面覆盖的膜层使得所述发泡垫具备良好的柔韧匹配性的同时,也满足密封功能性要求,其邵氏A硬度为35-50,用于瓶盖垫片具有优异的密封性及良好的开启性能,并具有粘结与提高平整度的作用,另外,其为食品级塑料片;The foaming mat provided by the invention comprises a base layer and a film layer, the base layer is obtained by foaming, has good cross-linking sealing property, and has better flexibility, flexibility and elasticity, and the surface covered film layer makes the The foaming pad has good flexibility and meets the sealing functional requirements. Its Shore A hardness is 35-50. It has excellent sealing property and good opening performance for the cap gasket. And the effect of improving the flatness, in addition, it is a food grade plastic sheet;
本发明提供的发泡垫的制备方法简单,便于工业化应用。The foaming mat provided by the invention has a simple preparation method and is convenient for industrial application.
具体实施方式detailed description
下面通过具体实施方式来进一步说明本发明的技术方案。The technical solution of the present invention will be further described below by way of specific embodiments.
以下实施例的制备方法中,步骤(1)所述单螺杆挤出机为具有加热、冷却及耐压特性的单螺杆挤出机——贝尔斯托夫有限公司制造的发泡机:150-ISO-PAC。In the preparation method of the following examples, the single-screw extruder of the step (1) is a single-screw extruder having heating, cooling and pressure resistance characteristics - a foaming machine manufactured by Berstorff Co., Ltd.: 150- ISO-PAC.
以下实施例所述膜层的厚度为某一数值是指基体层的上表面膜层的厚度和下表面膜层的厚度独立地为某一数值。The thickness of the film layer described in the following examples is a numerical value means that the thickness of the upper surface film layer of the base layer and the thickness of the lower surface film layer are independently a certain value.
实施例1Example 1
一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,毛细孔的平均直径为1-30μm;所述膜层为淋膜层,膜层均匀致密;所述基体层的厚度为0.5mm;所述膜层的 厚度为0.02mm;A foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 1 to 30 μm; the film layer is uniform and dense; the thickness of the substrate layer is 0.5 mm; The thickness is 0.02 mm;
所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000004
Figure PCTCN2016111474-appb-000004
所述脱模剂选自油酸酰胺;The release agent is selected from the group consisting of oleic acid amide;
所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。The nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000005
Figure PCTCN2016111474-appb-000005
所述增粘剂选自EEA(乙烯丙烯酸乙酯)。The tackifier is selected from the group consisting of EEA (ethylene acrylate).
所述脱模剂选自油酸酰胺。The release agent is selected from oleic acid amides.
所述开口剂选自芥酸酰胺。The opening agent is selected from the group consisting of erucamide.
所述发泡垫的制备方法包括如下步骤:The preparation method of the foaming pad comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入50bar压力下的超临界二氧化碳,超临界二氧化碳的流量为2.50kg/h,经挤出发泡,得到基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度65℃;挤出温度为210℃;挤出过程中螺杆的转速为1rpm;所述单螺杆挤出机的承压范围为250bar; (1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 50 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.50 kg/h. After extrusion foaming, a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 65 ° C; an extrusion temperature of 210 ° C; and a screw rotation speed of 1 rpm during extrusion; The screw extruder has a pressure range of 250 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.02mm的发泡垫,其中,挤出的温度为80℃;挤出过程中螺杆的转速为100rpm。(2) feeding the formulated amount of the film raw material into the hopper of the single-screw extruder, and coating the surface of the substrate layer to obtain a foaming pad having a film thickness of 0.02 mm, wherein the extrusion temperature is 80 ° C; The speed of the screw during the exit was 100 rpm.
实施例2Example 2
一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,毛细孔的平均直径为50-100μm;所述膜层为淋膜层,膜层均匀致密;所述基体层的厚度为10.0mm;所述膜层的厚度为0.15mm;A foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film layer of 50-100 μm; the film layer is uniform and dense; the thickness of the substrate layer is 10.0 mm; the thickness of the film layer is 0.15 mm;
所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000006
Figure PCTCN2016111474-appb-000006
所述脱模剂选自油酸酰胺与芥酸酰胺。The release agent is selected from the group consisting of oleic acid amides and erucamides.
优选地,所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。Preferably, the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000007
Figure PCTCN2016111474-appb-000007
所述增粘剂选自EEA与聚酯。The tackifier is selected from the group consisting of EEA and polyester.
所述脱模剂选自油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料。The release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
所述开口剂选自芥酸酰胺。The opening agent is selected from the group consisting of erucamide.
所述发泡垫的制备方法包括如下步骤:The preparation method of the foaming pad comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入220bar压力下的超临界二氧化碳,超临界二氧化碳的流量为0.10kg/h,经挤出发泡,得到基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度50℃;挤出温度为90℃;挤出过程中螺杆的转速为100rpm;所述单螺杆挤出机的承压范围为100bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 220 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 0.10 kg/h. After extrusion foaming, a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 50 ° C; an extrusion temperature of 90 ° C; and a screw rotation speed of 100 rpm during extrusion; The screw extruder has a pressure range of 100 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.15mm的发泡垫,其中,挤出的温度为250℃;挤出过程中螺杆的转速为1rpm。(2) feeding the film material of the formula amount into the hopper of the single-screw extruder, and coating the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.15 mm, wherein the extrusion temperature is 250 ° C; The speed of the screw during the exit was 1 rpm.
实施例3Example 3
一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,毛细孔的平均直径为30-80μm;所述膜层为淋膜层,膜层均匀致密;所述基体层的厚度为5.0mm;所述膜层的厚度为0.10mm;A foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 30-80 μm; the film layer is uniform and dense; the thickness of the substrate layer is 5.0 mm; the thickness of the film layer is 0.10 mm;
所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000008
Figure PCTCN2016111474-appb-000008
Figure PCTCN2016111474-appb-000009
Figure PCTCN2016111474-appb-000009
所述脱模剂选自芥酸酰胺。The release agent is selected from the group consisting of erucamide.
优选地,所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。Preferably, the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000010
Figure PCTCN2016111474-appb-000010
所述增粘剂选自马来酸酐接枝树脂。The tackifier is selected from the group consisting of maleic anhydride graft resins.
所述脱模剂选自油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料。The release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
所述开口剂选自芥酸酰胺。The opening agent is selected from the group consisting of erucamide.
所述发泡垫的制备方法包括如下步骤:The preparation method of the foaming pad comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入100bar压力下的超临界二氧化碳,超临界二氧化碳的流量为1.00kg/h,经挤出发泡,得到基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度60℃;挤出温度为120℃;挤出过程中螺杆的转速为20rpm;所述单螺杆挤出机的承压范围为120bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 100 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 1.00 kg/h. After extrusion foaming, a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 60 ° C; an extrusion temperature of 120 ° C; and a screw rotation speed of 20 rpm during extrusion; The screw extruder has a pressure range of 120 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.10mm的发泡垫,其中,挤出的温度为100℃;挤出过程中螺杆的转速为20rpm。 (2) feeding the film material of the formula amount into the hopper of the single-screw extruder, and coating the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.10 mm, wherein the extrusion temperature is 100 ° C; The speed of the screw during the exit was 20 rpm.
实施例4Example 4
一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,毛细孔的平均直径为1-30μm;所述膜层为淋膜层,膜层均匀致密;所述基体层的厚度为3.0mm;所述膜层的厚度为0.05mm;A foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores The film layer is a laminating layer, the film layer is uniform and dense; the thickness of the substrate layer is 3.0 mm; the thickness of the film layer is 0.05 mm;
所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000011
Figure PCTCN2016111474-appb-000011
所述脱模剂选自油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料。The release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。The nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000012
Figure PCTCN2016111474-appb-000012
优选地,所述增粘剂选自EEA、聚酯与马来酸酐接枝树脂按照质量比为 1∶1∶1的组合。Preferably, the tackifier is selected from the group consisting of EEA, polyester and maleic anhydride graft resin in terms of mass ratio A 1:1:1 combination.
所述脱模剂选自油酸酰胺。The release agent is selected from oleic acid amides.
所述开口剂选自芥酸酰胺。The opening agent is selected from the group consisting of erucamide.
所述发泡垫的制备方法包括如下步骤:The preparation method of the foaming pad comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入150bar压力下的超临界二氧化碳,超临界二氧化碳的流量为2.0kg/h,经挤出发泡,得到基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度55℃;挤出温度为170℃;挤出过程中螺杆的转速为80rpm;所述单螺杆挤出机的承压范围为150bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 150 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.0 kg/h. After extrusion foaming, a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 55 ° C; an extrusion temperature of 170 ° C; and a screw rotation speed of 80 rpm during extrusion; The screw extruder has a pressure range of 150 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.05mm的发泡垫,其中,挤出的温度为180℃;挤出过程中螺杆的转速为90rpm。(2) feeding the film material of the formula amount into the hopper of the single-screw extruder, and coating the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.05 mm, wherein the extrusion temperature is 180 ° C; The speed of the screw during the exit was 90 rpm.
实施例5Example 5
一种发泡垫,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,毛细孔的平均直径为1-100μm;所述膜层为淋膜层,膜层均匀致密;所述基体层的厚度为3.0mm;所述膜层的厚度为0.05mm;A foaming mat comprising a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary pore-shaped body, an average diameter of the capillary pores a film thickness of 1-100 μm; the film layer is uniform and dense; the thickness of the substrate layer is 3.0 mm; the thickness of the film layer is 0.05 mm;
所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000013
Figure PCTCN2016111474-appb-000013
Figure PCTCN2016111474-appb-000014
Figure PCTCN2016111474-appb-000014
所述脱模剂选自油酸酰胺。The release agent is selected from oleic acid amides.
所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。The nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and PE or PP or EVA as a carrier.
所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
Figure PCTCN2016111474-appb-000015
Figure PCTCN2016111474-appb-000015
所述增粘剂选自马来酸酐接枝树脂。The tackifier is selected from the group consisting of maleic anhydride graft resins.
所述脱模剂选自油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料。The release agent is selected from the group consisting of oleic acid amide and erucamide, and a masterbatch based on PE or PP.
所述开口剂选自芥酸酰胺。The opening agent is selected from the group consisting of erucamide.
所述发泡垫的制备方法包括如下步骤:The preparation method of the foaming pad comprises the following steps:
(1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入150bar压力下的超临界二氧化碳,超临界二氧化碳的流量为2.0kg/h,经挤出发泡,得到基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度55℃;挤出温度为170℃;挤出过程中螺杆的转速为80rpm;所述单螺杆挤出机的承压范围为150bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 150 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 2.0 kg/h. After extrusion foaming, a base layer is obtained, wherein the single screw extruder in the extrusion process has a host temperature of 55 ° C; an extrusion temperature of 170 ° C; and a screw rotation speed of 80 rpm during extrusion; The screw extruder has a pressure range of 150 bar;
(2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.05mm的发泡垫,其中,挤出的温度为180℃;挤出过程中螺杆的转速为90rpm。 (2) feeding the film material of the formula amount into the hopper of the single-screw extruder, and coating the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.05 mm, wherein the extrusion temperature is 180 ° C; The speed of the screw during the exit was 90 rpm.
对比例1Comparative example 1
所述对比例1为实施例3制得的基体层。The comparative example 1 is the base layer obtained in Example 3.
对比例2Comparative example 2
所述对比例2为商购的PE垫片(生产厂家:上海明渊塑料制品有限公司)。The comparative example 2 is a commercially available PE gasket (manufacturer: Shanghai Mingyuan Plastic Products Co., Ltd.).
对比例3Comparative example 3
一种发泡垫及其制备方法,除超临界二氧化碳的流量为0.08kg/h外,其余与实施例5相同。A foaming pad and a preparation method thereof are the same as those in Embodiment 5 except that the flow rate of supercritical carbon dioxide is 0.08 kg/h.
对比例4Comparative example 4
一种发泡垫及其制备方法,除超临界二氧化碳的流量为2.60kg/h外,其余与实施例5相同。A foaming pad and a preparation method thereof are the same as in the embodiment 5 except that the flow rate of the supercritical carbon dioxide is 2.60 kg/h.
对实施例1-5及对比例1-4得到的产品进行性能测试,密度的测试方法为GB1033,柔韧性的测试方法为感性测试,邵氏硬度的测试方法为GB2411,密封性的测试方法为自制渗油法(用发泡垫制作的瓶盖密封装满食用油的玻璃瓶,侧放于铺有白纸的平台上,10天后观察白纸上是否渗油,渗油为不合格,不渗油为合格)。测试结果如下表1所示:The products obtained in Examples 1-5 and Comparative Examples 1-4 were tested for performance. The density test method was GB1033, the flexibility test method was the inductive test, the Shore hardness test method was GB2411, and the seal test method was Self-made oil-infiltration method (the bottle cap made of foaming pad is sealed with glass bottle filled with edible oil, placed on the platform with white paper on the side, and after 10 days, it is observed whether there is oil leakage on the white paper, the oil seepage is unqualified, no The oil seepage is acceptable). The test results are shown in Table 1 below:
表1Table 1
  密度density 柔韧性Flexibility 邵氏A硬度Shore A hardness 用于瓶盖垫片的密封性Sealing for cap gaskets
实施例1Example 1 300g/L300g/L 优良excellent 5050 合格qualified
实施例2Example 2 288g/L288g/L 良好good 5151 合格qualified
实施例3Example 3 425g/L425g/L 优良excellent 4545 合格qualified
实施例4Example 4 403g/L403g/L 良好good 4848 合格qualified
实施例5Example 5 389g/L389g/L 优良excellent 3535 合格qualified
对比例1Comparative example 1 305g/L305g/L 一般general 5757 合格qualified
对比例2Comparative example 2 297g/L297g/L 一般general 6060 合格qualified
对比例3Comparative example 3 412g/L412g/L 一般general 6565 合格qualified
对比例4Comparative example 4 263g/L263g/L 一般general 6262 合格qualified
可见,本发明提供的发泡垫,其性能优异,用于瓶盖垫片的密封性能极佳。另外,本发明提供的发泡垫,其达到食品级要求,可广泛用于食品包装、药品包装等高安全领域。It can be seen that the foaming pad provided by the invention has excellent performance and excellent sealing performance for the cap gasket. In addition, the foaming pad provided by the invention meets food grade requirements and can be widely used in high security fields such as food packaging and pharmaceutical packaging.
申请人声明,本发明通过上述实施例来说明本发明的详细方法,但本发明并不局限于上述详细方法,即不意味着本发明必须依赖上述详细方法才能实施。所属技术领域的技术人员应该明了,对本发明的任何改进,对本发明产品各原料的等效替换及辅助成分的添加、具体方式的选择等,均落在本发明的保护范围和公开范围之内。 The Applicant declares that the present invention is described by the above-described embodiments, but the present invention is not limited to the above detailed methods, that is, it does not mean that the present invention must be implemented by the above detailed methods. It should be apparent to those skilled in the art that any modifications of the present invention, equivalent substitution of the various materials of the products of the present invention, addition of auxiliary components, selection of specific means, and the like, are all within the scope of the present invention.

Claims (12)

  1. 一种发泡垫,其特征在于,所述发泡垫包括基体层和覆盖于基体层上表面和下表面的膜层,所述基体层为发泡体,且为均匀毛细孔状体,所述毛细孔的平均孔径为1-100μm;A foaming mat, comprising: a base layer and a film layer covering the upper surface and the lower surface of the base layer, the base layer being a foam and being a uniform capillary body, The average pore diameter of the pores is 1-100 μm;
    所述基体层按质量百分含量主要由如下原料制备得到:The base layer is mainly prepared from the following raw materials in terms of mass percentage:
    Figure PCTCN2016111474-appb-100001
    Figure PCTCN2016111474-appb-100001
    其中,PE和PP中至多一种物质的质量百分含量为0;Wherein, the mass percentage of at most one of the PE and the PP is 0;
    所述膜层按质量百分含量主要由如下原料制备得到:The film layer is mainly prepared from the following raw materials in terms of mass percentage:
    Figure PCTCN2016111474-appb-100002
    Figure PCTCN2016111474-appb-100002
    其中,PE、PP和POE中至多一种物质的质量百分含量为0。Among them, the mass percentage of at most one of PE, PP and POE is zero.
  2. 根据权利要求1所述的发泡垫,其特征在于,所述基体层按质量百分含量由如下原料制备得到:The foaming mat according to claim 1, wherein the base layer is prepared in a mass percentage from the following materials:
    Figure PCTCN2016111474-appb-100003
    Figure PCTCN2016111474-appb-100003
    Figure PCTCN2016111474-appb-100004
    Figure PCTCN2016111474-appb-100004
  3. 根据权利要求1或2所述的发泡垫,其特征在于,所述脱模剂选自油酸酰胺、芥酸酰胺或油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料中的任意一种或至少两种的组合。The foaming pad according to claim 1 or 2, wherein the releasing agent is selected from the group consisting of oleic acid amide, erucic acid amide or oleic acid amide and erucamide, and a masterbatch based on PE or PP. Any one or a combination of at least two.
  4. 根据权利要求1-3之一所述的发泡垫,其特征在于,所述成核剂选自以碳酸氢钠和柠檬酸为主要有效成分,以PE或PP或EVA为载体的母料。A foaming mat according to any one of claims 1 to 3, wherein the nucleating agent is selected from the group consisting of sodium bicarbonate and citric acid as main active ingredients, and a masterbatch based on PE or PP or EVA.
  5. 根据权利要求1-4之一所述的发泡垫,其特征在于,所述膜层按质量百分含量主要由如下原料制备得到:The foaming mat according to any one of claims 1 to 4, characterized in that the film layer is mainly prepared from the following raw materials by mass percentage:
    Figure PCTCN2016111474-appb-100005
    Figure PCTCN2016111474-appb-100005
    优选地,所述增粘剂选自EEA、聚酯或马来酸酐接枝树脂中的任意一种或至少两种的组合;Preferably, the tackifier is selected from any one or a combination of at least two of EEA, polyester or maleic anhydride graft resin;
    优选地,所述脱模剂选自油酸酰胺、芥酸酰胺或油酸酰胺与芥酸酰胺制作的以PE或PP为载体的母料中的任意一种或至少两种的组合;Preferably, the release agent is selected from the group consisting of oleic acid amide, erucic acid amide or oleic acid amide with erucamide and any combination of at least two of a masterbatch based on PE or PP;
    优选地,所述开口剂选自芥酸酰胺。 Preferably, the opening agent is selected from the group consisting of erucamide.
  6. 根据权利要求1-5之一所述的发泡垫,其特征在于,所述基体层的厚度为0.5-10.0mm;The foaming pad according to any one of claims 1 to 5, wherein the base layer has a thickness of 0.5 to 10.0 mm;
    优选地,所述基体层的密度为100-800kg/m3Preferably, the base layer has a density of 100-800 kg/m 3 ;
    优选地,所述膜层的厚度为0.02-0.15mm。Preferably, the film layer has a thickness of from 0.02 to 0.15 mm.
  7. 根据权利要求1-6之一所述的发泡垫的制备方法,其特征在于,所述制备方法包括如下步骤:The method for preparing a foaming mat according to any one of claims 1 to 6, wherein the preparation method comprises the following steps:
    (1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入超临界二氧化碳,经挤出发泡,得到基体层,所述超临界二氧化碳为50-220bar压力下的超临界二氧化碳;(1) feeding the formulated amount of the base layer raw material into the hopper of the single-screw extruder, simultaneously charging the central portion of the single-screw extruder with supercritical carbon dioxide, and extruding and foaming to obtain a base layer, the supercritical carbon dioxide Supercritical carbon dioxide at a pressure of 50-220 bar;
    (2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到所述发泡垫。(2) The formulated amount of the film raw material is fed into a single-screw extruder hopper, and a film is deposited on the surface of the base layer to obtain the foamed mat.
  8. 根据权利要求7所述的制备方法,其特征在于,步骤(1)所述挤出过程中单螺杆挤出机的主机温度≤65℃;The preparation method according to claim 7, wherein the main screw temperature of the single-screw extruder in the extrusion process in the step (1) is ≤ 65 ° C;
    优选地,步骤(1)所述挤出温度为90-210℃;Preferably, the extrusion temperature in step (1) is 90-210 ° C;
    优选地,步骤(1)所述挤出过程中螺杆的转速为1-100rpm;Preferably, the speed of the screw in the extrusion process in the step (1) is 1-100 rpm;
    优选地,步骤(1)所述单螺杆挤出机的承压范围为0-250bar。Preferably, the single screw extruder of step (1) has a pressure range of 0-250 bar.
  9. 根据权利要求7或8所述的制备方法,其特征在于,步骤(1)所述超临界二氧化碳的流量为0.10-2.50kg/h;The preparation method according to claim 7 or 8, wherein the flow rate of the supercritical carbon dioxide in the step (1) is 0.10-2.50 kg / h;
    优选地,步骤(1)所述基体层的厚度为0.5-10.0mm;Preferably, the thickness of the base layer in step (1) is 0.5-10.0 mm;
    优选地,步骤(1)所述基体层的密度为100-800kg/m3Preferably, the density of the base layer in the step (1) is from 100 to 800 kg/m 3 .
  10. 根据权利要求7-9之一所述的制备方法,其特征在于,步骤(2)所述挤出的温度为80-250℃;The preparation method according to any one of claims 7-9, characterized in that the temperature of the extrusion in the step (2) is 80-250 ° C;
    优选地,步骤(2)所述挤出过程中螺杆的转速为1-100rpm。 Preferably, the rotation speed of the screw during the extrusion in the step (2) is 1-100 rpm.
  11. 根据权利要求7-10之一所述的制备方法,其特征在于,步骤(2)所述基体层覆膜厚度为0.02-0.15mm。The preparation method according to any one of claims 7 to 10, wherein the base layer coating film has a thickness of 0.02 to 0.15 mm in the step (2).
  12. 根据权利要求7-11之一所述的制备方法,其特征在于,所述制备方法包括如下步骤:The preparation method according to any one of claims 7 to 11, characterized in that the preparation method comprises the following steps:
    (1)将配方量的基体层原料送入单螺杆挤出机的料斗中,同时向单螺杆挤出机中部充入50-220bar压力下的超临界二氧化碳,超临界二氧化碳的流量为0.10-2.50kg/h,经挤出发泡,得到密度为100-800kg/m3,厚度为0.5-10.0mm的基体层,其中,所述挤出过程中的单螺杆挤出机的主机温度≤65℃;挤出温度为90-210℃;挤出过程中螺杆的转速为1-100rpm;所述单螺杆挤出机的承压范围为0-250bar;(1) The formulated amount of the base layer raw material is fed into the hopper of the single-screw extruder, and the supercritical carbon dioxide under the pressure of 50-220 bar is charged into the middle of the single-screw extruder, and the flow rate of the supercritical carbon dioxide is 0.10-2.50. Kg/h, after extrusion foaming, to obtain a substrate layer having a density of 100-800 kg/m 3 and a thickness of 0.5-10.0 mm, wherein the host temperature of the single-screw extruder during the extrusion process is ≤65 ° C The extrusion temperature is 90-210 ° C; the speed of the screw during extrusion is 1-100 rpm; the pressure range of the single-screw extruder is 0-250 bar;
    (2)将配方量的膜层原料送入单螺杆挤出机料斗中,在基体层表面淋膜,得到覆膜厚度为0.02-0.15mm的发泡垫,其中,挤出的温度为80-250℃;挤出过程中螺杆的转速为1-100rpm。 (2) The film material of the formula amount is sent into the hopper of the single-screw extruder, and the film is coated on the surface of the substrate layer to obtain a foaming pad with a film thickness of 0.02-0.15 mm, wherein the extrusion temperature is 80- 250 ° C; the speed of the screw during extrusion is 1-100 rpm.
PCT/CN2016/111474 2016-08-12 2016-12-22 Foam pad and preparation method therefor WO2018028111A1 (en)

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