US20010035593A1 - Sealable, biaxially oriented polyester film - Google Patents

Sealable, biaxially oriented polyester film Download PDF

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Publication number
US20010035593A1
US20010035593A1 US09/818,878 US81887801A US2001035593A1 US 20010035593 A1 US20010035593 A1 US 20010035593A1 US 81887801 A US81887801 A US 81887801A US 2001035593 A1 US2001035593 A1 US 2001035593A1
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Prior art keywords
layer
film
sealable
range
polyester film
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US09/818,878
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US6423401B2 (en
Inventor
Herbert Peiffer
Richard Davis
Gottfried Hilkert
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Mitsubishi Polyester Film GmbH
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Mitsubishi Polyester Film GmbH
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Priority to DE10015633.9 priority Critical
Priority to DE2000115633 priority patent/DE10015633A1/en
Priority to DE10015633 priority
Application filed by Mitsubishi Polyester Film GmbH filed Critical Mitsubishi Polyester Film GmbH
Assigned to MITSUBISHI POLYESTER FILM GMBH reassignment MITSUBISHI POLYESTER FILM GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DAVIS, RICHARD LEE, HILKERT, GOTTFRIED, PEIFFER, HERBERT
Publication of US20010035593A1 publication Critical patent/US20010035593A1/en
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Classifications

    • 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
    • B29C55/00Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/02Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
    • B29C55/10Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial
    • B29C55/12Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial
    • B29C55/14Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial successively
    • B29C55/143Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial successively firstly parallel to the direction of feed and then transversely thereto
    • 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
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • 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
    • B29K2067/00Use of polyesters or derivatives thereof, as moulding material
    • 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0072Roughness, e.g. anti-slip
    • 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
    • B32B38/00Ancillary operations in connection with laminating processes
    • B32B38/0012Mechanical treatment, e.g. roughening, deforming, stretching
    • B32B2038/0028Stretching, elongating
    • 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
    • B32B2307/514Oriented
    • B32B2307/518Oriented bi-axially
    • 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
    • B32B2310/00Treatment by energy or chemical effects
    • B32B2310/14Corona, ionisation, electrical discharge, plasma treatment
    • 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
    • B32B2367/00Polyesters, e.g. PET, i.e. polyethylene terephthalate
    • 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
    • B32B2553/00Packaging equipment or accessories not otherwise provided for
    • 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
    • B32B37/00Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/15Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
    • B32B37/153Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
    • 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
    • B32B38/00Ancillary operations in connection with laminating processes
    • B32B38/0008Electrical discharge treatment, e.g. corona, plasma treatment; wave energy or particle radiation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/91Product with molecular orientation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495Thickness [relative or absolute]
    • Y10T428/24967Absolute thicknesses specified
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495Thickness [relative or absolute]
    • Y10T428/24967Absolute thicknesses specified
    • Y10T428/24975No layer or component greater than 5 mils thick
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/254Polymeric or resinous material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • Y10T428/2817Heat sealable
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • Y10T428/2817Heat sealable
    • Y10T428/2826Synthetic resin or polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2848Three or more layers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31786Of polyester [e.g., alkyd, etc.]

Abstract

The invention relates to a biaxially oriented, sealable polyester film with at least a base layer (B), with a sealable outer layer (A) and with another, nonsealable outer layer (C), where the sealable outer layer (A) has a minimum sealing temperature of not more than 110° C. and a seal seam strength of at least 1.3 N/15 mm of film width, and the topographies of the two outer layers (A) and (C) have particular characterizing features. The film of the invention is particularly suitable for use in flexible packaging and specifically in particular for use on high-speed packaging machinery.

Description

  • The invention relates to a transparent, sealable, coextruded, biaxially oriented polyester film composed of at least a base layer (B) and, applied to the two sides of this base layer, outer layers (A) and (C). The invention also relates to the use of the film, and to a process for its production. [0001]
  • BACKGROUND OF THE INVENTION
  • Sealable, biaxially oriented polyester films are known in the prior art. These known prior art films either have good sealing performance or good optical properties or acceptable processing performance. [0002]
  • GB-A 1 465 973 describes a coextruded, two-layer polyester film, one layer of which is composed of copolyesters containing isophthalic and terephthalic acids and the other layer of which is composed of polyethylene terephthalate. No useful information is given in the specification concerning the sealing performance of the film. Due to lack of pigmentation, the film cannot be produced reliably (cannot be wound), and its capability for further processing is limited. [0003]
  • EP-A 0 035 835 describes a coextruded sealable polyester film where, to improve the winding and processing characteristics, the sealing layer contains particles whose average particle size exceeds the thickness of the sealing layer. The particulate additives create surface protrusions preventing the undesirable blocking and sticking of the film to rolls or guides. No further information is provided on the incorporation of antiblocking agents with regard to the other, nonsealable layer of the film. It remains moot whether this layer contains antiblocking agents. Choosing particles having a larger diameter than the sealing layer and the concentrations reported in the examples has an adverse effect on the sealing characteristics of the film. The reference provides no information on the sealing temperature range of the film. The seal seam strength is measured at 140° C. and found to be in the range from 63 to 120 N/m (which corresponds to 0.97 to 1.8 N/15 mm of film width). [0004]
  • EP-A 0 432 886 describes a coextruded, multilayer polyester film which has a first surface on which has been arranged a sealable layer, and has a second surface on which has been arranged an acrylate layer. The sealable outer layer here may also be composed of isophthalic-acid-containing and terephthalic-acid-containing copolyesters. The coating on the reverse side gives the film improved processing performance. The patent gives no indication of the sealing range of the film. The seal seam strength is measured at 140° C. For a sealable layer thickness of 11 μm the seal seam strength given is 761.5 N/m (11.4 N/15 mm). A disadvantage of the reverse-side acrylate coating is that this side is now not sealable with respect to the sealable outer layer, and the film therefore has only very restricted use. [0005]
  • EP-A 0 515 096 describes a coextruded, multilayer, sealable polyester film which comprises a further additive on the sealable layer. The additive may comprise inorganic particles, for example, and is preferably applied in an aqueous layer to the film during its production. Using this method, the film is claimed to retain its good sealing properties and to be easy to process. The reverse side comprises only very few particles, most of which pass into this layer via the recycled material. This patent again gives no indication of the sealing temperature range of the film. The seal seam strength is measured at 140° C. and is above 200 N/m (3 N/15 mm). For a sealable layer of 3 μm thickness the seal seam strength given is 275 N/m (4.125 N/15 mm). [0006]
  • WO 98/06575 describes a coextruded, multilayer polyester film which comprises a sealable outer layer and a nonsealable base layer. The base layer here may have been built up from one or more layers, and one of these layers is in contact with the sealable layer. The other (outward-facing) layer then forms the second nonsealable outer layer. Here, too, the sealable outer layer may be composed of isophthalic-acid-containing and terephthalic-acid-containing copolyesters, but these comprise no antiblocking particles. The film also comprises at least one UV absorber, which is added to the base layer in a weight ratio of from 0.1 to 10%. The base layer of this film has conventional antiblocking agents. The film has good sealability, but does not have the desired processing performance and has shortcomings in optical properties (gloss and haze). [0007]
  • It was therefore an object of the present invention to provide a sealable, biaxially oriented polyester film which does not have the disadvantages of the prior art films mentioned and which in particular has improved sealability and improved processability, while otherwise its optical properties remain the same or even improve. It was a particular object of the present invention to extend the sealing range of the film toward low temperatures, and to improve the seal seam strength of the film. In addition, the film was also to be processable on high-speed processing machinery. It should also be ensured that any cut material arising during film production can be reintroduced as recycled material to the production process in amounts of up to 60% by weight, based on the total weight of the film, without adversely affecting the physical or optical properties of the film. [0008]
  • SUMMARY OF THE INVENTION
  • According to the invention, the object is achieved by providing a coextruded, biaxially oriented, sealable polyester film with at least a base layer (B), with a sealable outer layer (A) and with another outer layer (C), where the sealable outer layer A has a minimum sealing temperature of not more than 110° C. and a seal seam strength of at least 1.3 N/15 mm of film width, and the topograhies of the two outer layers (A) and (C) have the following features: [0009]
  • Sealable outer layer (A): [0010]
  • R[0011] a≦40 nm
  • Value measured for gas flow within the range from 300 to 4000 s. [0012]
  • Nonsealable outer layer (C): [0013]
  • COF≦0.5 [0014]
  • 40 nm≦R[0015] a≦150 nm
  • Value measured for gas flow≦140 s. [0016]
  • Number of elevations N[0017] c per mm2 of film surface correlated with their respective heights h via the following equations:
  • A c1 −B c1·log h/μm<log N c /mm 2 <A c2 −B c2·log h/μm 0.01 μm≦h≦10 μm
  • Ac1=0.29 Bc1=3.30
  • Ac2=1.84 Bc2=2.70.
  • The subclaims give preferred embodiments of the invention, and these are described in more detail below. [0018]
  • DETAILED DESCRIPTION OF THE INVENTION
  • According to the invention, the film has at least three layers and then embraces the base layer (B), the sealable outer layer (A) and the nonsealable outer layer (C). [0019]
  • Polymers used for the base and for the outer layer: [0020]
  • Base material: [0021]
  • At least 90% by weight of the base layer (B) is preferably composed of a thermoplastic polyester. Polyesters suitable for this purpose are those made from ethylene glycol and terephthalic acid (polyethylene terephthalate, PET), from ethylene glycol and naphthalene-2,6-dicarboxylic acid (polyethylene 2,6-naphthalate, PEN), from 1,4-bishydroxymethylcyclohexane and terephthalic acid (poly-1,4-cyclohexanedimethylene terephthalate, PCDT), or else made from ethylene glycol, naphthalene-2,6-dicarboxylic acid and biphenyl-4,4′-dicarboxylic acid (polyethylene 2,6-naphthalate dibenzoate, PENBB). Particular preference is given to polyesters at least 90 mol %, preferably at least 95 mol %, of which is composed of ethylene glycol units and terephthalic acid units, or of ethylene glycol units and naphthalene-2,6-dicarboxylic acid units. The remaining monomer units derive from other aliphatic, cycloaliphatic or aromatic diols and, respectively, dicarboxylic acids, as may also occur in the layer (A) or in the layer (C). [0022]
  • Other examples of suitable aliphatic diols are diethylene glycol, triethylene glycol, aliphatic glycols of the formula HO—(CH[0023] 2)n—OH, where n is an integer from 3 to 6 (in particular 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol and 1,6-hexanediol) and branched aliphatic glycols having up to 6 carbon atoms. Among the cycloaliphatic diols, mention should be made of cyclohexanediols (in particular 1,4-cyclohexanediol). Examples of other suitable aromatic diols have the formula HO—C6H4—X—C6H4—OH, where X is —CH2—, —C(CH3)2—, —C(CF3)2—, —O—, —S— or —SO2—. Bisphenols of the formula HO—C6H4—C6H4—OH are also very suitable.
  • Other aromatic dicarboxylic acids are preferably benzenedicarboxylic acids, naphthalene dicarboxylic acids (such as naphthalene-1,4- or -1,6-dicarboxylic acid), biphenyl-x,x′-dicarboxylic acids (in particular biphenyl-4,4′-dicarboxylic acid), diphenylacetylene-x,x′-dicarboxylic acids (in particular diphenylacetylene-4,4′-dicarboxylic acid) or stilbene-x,x′-dicarboxylic acids. Among the cycloaliphatic dicarboxylic acids mention should be made of cyclohexanedicarboxylic acids (in particular cyclohexane-1,4-dicarboxylic acid). Among the aliphatic dicarboxylic acids, the C[0024] 3-C19 alkanediacids are particularly suitable, and the alkane moiety here may be straight-chain or branched.
  • One way of preparing the polyesters is the transesterification process. Here, the starting materials are dicarboxylic esters and diols, which are reacted using the customary transesterification catalysts, such as the salts of zinc, of calcium, of lithium, of magnesium or of manganese. The intermediates are then polycondensed in the presence of well-known polycondensation catalysts, such as antimony trioxide or titanium salts. Another equally good preparation method is the direct esterification process in the presence of polycondensation catalysts. This starts directly from the dicarboxylic acids and the diols. [0025]
  • Sealable outer layer (A): [0026]
  • The sealable outer layer (A) applied by coextrusion to the base layer (B) is based on polyester copolymers and essentially consists of copolyesters composed predominantly of isophthalic acid units and of terephthalic acid units and of ethylene glycol units. The remaining monomer units are derived from other aliphatic, cycloaliphatic or aromatic diols and, respectively, dicarboxylic acids, as may also be present in the base layer. The preferred copolyesters which provide the desired sealing properties are those composed of ethylene terephthalate units and ethylene isophthalate units, and of ethylene glycol units. The proportion of ethylene terephthalate is from 40 to 95 mol % and the corresponding proportion of ethylene isophthalate is from 60 to 5 mol %. Preference is given to copolyesters in which the proportion of ethylene terephthalate is from 50 to 90 mol % and the corresponding proportion of ethylene isophthalate is from 50 to 10 mol %, and very particular preference is given to copolyesters in which the proportion of ethylene terephthalate is from 60 to 85 mol % and the corresponding proportion of ethylene isophthalate is from 40 to 15 mol %. [0027]
  • Nonsealable outer layer (C): [0028]
  • For the other, nonsealable outer layer (C), or for any other intermediate layers present, use in principle may be made of the same polymers as described above for the base layer (B). [0029]
  • Sealing and processing properties: [0030]
  • The desired sealing and processing properties of the film of the invention are obtained from the properties of the copolyester used for the sealable outer layer combined with the topographies of the sealable outer layer (A) and the nonsealable outer layer (C). [0031]
  • The minimum sealing temperature of not more than 110° C. and the seal seam strength of at least 1.3 N/15 mm of film width are achieved when the copolymers more particularly described above are used for the sealable outer layer (A). The best sealing properties for the film are achieved when no other additives, in particular no inorganic or organic fillers, are added to the copolymer. For a given copolyester, this gives the lowest minimum sealing temperature and the highest seal seam strengths. However, in this case the handling of the film is poor, since the surface of the sealable outer layer (A) has a marked tendency to block. The film is difficult to wind and is not at all suitable for further processing on high-speed packaging machinery. To improve the handling of the film and its processability it is necessary to modify the sealable outer layer (A). This is best done with the aid of suitable antiblocking agents of selected size, a certain amount of which is added to the sealable layer, and specifically in such a way as firstly to minimize blocking of the film and secondly to bring about only insignificant impairment of the sealing properties. Surprisingly, this desired combination of properties can be achieved when the topography of the sealable outer layer (A) is characterized by the following set of parameters: [0032]
  • According to the invention, the roughness of the sealable outer layer, expressed by the R[0033] a, should be less than or equal to 40 nm. Otherwise the sealing properties for the purposes of the present invention are adversely affected.
  • According to the invention, the value measured for gas flow should be within the range from 300 to 4000 s. At values below 300 s, the sealing properties for the purposes of the present invention are adversely affected, while at values above 4000 s the handling of the film is impaired. [0034]
  • For further improvement in the processing properties of the sealable film, the topography of the nonsealable outer layer (C) should be characterized by the following set of parameters: [0035]
  • According to the invention, the coefficient of friction (COF) of this side with respect to itself should be less than or equal to 0.5. Otherwise the winding performance and further processing of the film are unsatisfactory. [0036]
  • The roughness of the nonsealable outer layer (C), expressed as its R[0037] a, should be greater than or equal to 40 nm and less than or equal to 150 nm. Ra values below 40 nm have adverse effects on the winding and processing performance of the film, while Ra values above 150 nm impair the optical properties (gloss, haze) of the film.
  • According to the invention, the value measured for gas flow for the outer layer (C) should be within the range below 140 s. At values above 140 s, the winding and processing performance of the film is adversely affected. [0038]
  • The number of elevations N per mm[0039] 2 of film surface is correlated with their respective heights h via the following equation:
  • 0.29−3.30·log h/μm<log N/mm 2<1.84−2.70·log h/μm
  • where[0040]
  • 0.01 μm≦h≦10 μm
  • If the values for N are smaller than given by the left-hand side of the inequality, the winding and processing performance of the film is adversely affected, and if the values for N are greater than given by the right-hand side of the inequality, the gloss and the haze of the film are adversely affected. [0041]
  • Antiblocking agents [0042]
  • The base layer (B) may also comprise conventional additives, such as stabilizers and/or antiblocking agents. The two other layers (A) and (C) may also comprise conventional additives, such as stabilizers and/or antiblocking agents. It is expedient to add the agents to the polymer or to the polymer mixture prior to melting. The stabilizers used advantageously comprise phosphorus compounds, for example, such as phosphoric acid or phosphoric esters. [0043]
  • Typical antiblocking agents (in this context also termed “pigments”) are inorganic or organic particles, such as calcium carbonate, amorphous silica, talc, magnesium carbonate, barium carbonate, calcium sulfate, barium sulfate, lithium phosphate, calcium phosphate, magnesium phosphate, aluminum oxide, LiF, the calcium, barium, zinc or manganese salts of the dicarboxylic acids used, carbon black, titanium dioxide, kaolin, or crosslinked polystyrene particles or crosslinked acrylate particles. [0044]
  • The antiblocking agents selected may also be mixtures of two or more different antiblocking agents or mixtures of antiblocking agents of the same composition but of different particle size. The particles may be added to each layer in respective advantageous concentrations, e.g. as a glycolic dispersion during the polycondensation, or by way of masterbatches during extrusion. [0045]
  • Preferred particles are SiO[0046] 2 in colloidal or in chain form. These particles become very well bound into the polymer matrix and create only very few vacuoles. Vacuoles generally cause haze and it is therefore appropriate to avoid these. There is no restriction in principle on the diameters of the particles used. However, it has proven appropriate for achieving the object to use particles with an average primary particle diameter below 100 nm, preferably below 60 nm and particularly preferably below 50 nm, measured by the sedigraph method, and/or particles with an average primary particle diameter not less than 1 μm, preferably not less than 1.5 μm and particularly preferably not less than 2 μm. However, the average particle diameter of these particles described last should not be above 5 μm.
  • To achieve the abovementioned properties of the sealable film, it has also proven to be appropriate to select a particle concentration in the base layer B which is lower than in the two outer layers (A) and (C) . In a three-layer film of the type mentioned the particle concentration in the base layer (B) will be from 0 to 0.15% by weight, preferably from 0 to 0.12% by weight and in particular from 0 to 0.10% by weight. There is no restriction in principle on the diameter of the particles used, but particular preference is given to particles with an average diameter not less than 1 μm. [0047]
  • In its advantageous usage form, the film is composed of three layers: the base layer (B) and, applied on both sides of this base layer, outer layers (A) and (C), and outer layer (A) is sealable with respect to itself and with respect to outer layer (C). [0048]
  • To achieve the property profile mentioned for the film, the outer layer (C) has more pigments (i.e. a higher pigment concentration) than the outer layer (A). According to the invention, the pigment concentration in this second outer layer (C) is from 0.1 to 1.0% by weight, advantageously from 0.12 to 0.8% by weight and in particular from 0.15 to 0.6% by weight. In contrast, the other outer layer (A), which is sealable and positioned opposite to the outer layer (C), has a lower degree of filling with inert pigments. The concentration of the inert particles in layer (A) is from 0.01 to 0.2% by weight, preferably from 0.015 to 0.15% by weight and in particular from 0.02 to 0.1% by weight, all weight % ages being based on the total weight of the respective layer. [0049]
  • Between the base layer and the outer layers there may, if desired, also be an intermediate layer. This may again be composed of the polymers described for the base layers. In one particularly preferred embodiment, the intermediate layer is composed of the polyester used for the base layer. The intermediate layer may also comprise the customary additives described. The thickness of the intermediate layer is generally above 0.3 μm, preferably in the range from 0.5 to 15 μm, in particular in the range from 1.0 to 10 μm and particularly preferably in the range from 1.0 to 5 μm. [0050]
  • In the particularly advantageous three-layer embodiment of the novel film, the thickness of the outer layers (A) and (C) is generally above 0.1 μm, and is generally in the range from 0.2 to 4.0 μm. particularly preferably in the range from 0.2 to 3.5 μm, in particular in the range from 0.3 to 3 μm and very particularly preferably in the range from 0.3 to 2.5 μm, and the thicknesses of the outer layers (A) and (C) may be identical or different. [0051]
  • The total thickness of the novel polyester film may vary within wide limits. It is from 3 to 80 μm, in particular from 4 to 50 μm, preferably from 5 to 30 μm, the layer (B) preferably making up from 5 to 90% of the total thickness. [0052]
  • In producing the film, the polymers for the base layer B and the two outer layers (A) and (C) are introduced to three extruders. Any foreign bodies or contamination present may be removed from the polymer melt by means of suitable filters prior to extrusion. The melts are then extruded in a coextrusion die to give flat melt films, and layered one upon the other. The multilayer film is then drawn off and solidified with the aid of a chill roll and, if desired, other rolls. [0053]
  • Production process: [0054]
  • The invention also provides a process for producing the polyester film of the invention by the coextrusion process known from the literature. [0055]
  • The procedure for this process is that the melts corresponding to the individual layers (A), (B) and (C) of the film are coextruded through a flat-film die, the resultant film is drawn off for solidification on one or more rolls, the film is then biaxially stretched (oriented), and the biaxially stretched film is heat-set and, if desired, corona- or flame-treated on the surface layer intended for treatment. [0056]
  • The biaxial stretching (orientation) is generally carried out sequentially, and preference is given to sequential biaxial stretching in which stretching is first longitudinal (in the machine direction) and then transverse (perpendicular to the machine direction). [0057]
  • As is usual in coextrusion, the polymer or the polymer mixture for the individual layers is first compressed and plasticized in an extruder, and any additives used may already be present in the polymer or the polymer mixture. [0058]
  • The melts are then simultaneously extruded through a flat-film die (slot die), and the extruded multilayer film is drawn off on one or more take-off rolls, whereupon it cools and solidifies. [0059]
  • The biaxial orientation is generally carried out sequentially, preferably orienting first longitudinally (i.e. in the machine direction=MD) and then transversely (i.e. perpendicularly to the machine direction=TD). This gives orientation of the molecular chains. The longitudinal orientation can be carried out with the aid of two rolls running at different speeds corresponding to the desired stretching ratio. For the transverse orientation use is generally made of an appropriate tenter frame, clamping both edges of the film and then drawing toward the two sides at an elevated temperature. [0060]
  • The temperature at which the orientation is carried out may vary over a relatively wide range and depends on the film properties desired. The longitudinal stretching is generally carried out at from about 80 to 130° C., and the transverse stretching at from about 80 to 150° C. The longitudinal stretching ratio is generally in the range from 2.5:1 to 6:1, preferably from 3:1 to 5.5:1. The transverse stretching ratio is generally in the range from 3.0:1 to 5.0:1, preferably from 3.5:1 to 4.5:1. Prior to the transverse stretching, one or both surfaces of the film may be in-line coated by known processes. The in-line coating may serve, for example, to give improved adhesion of a metal layer or of any printing ink applied, or else to improve antistatic performance or processing performance. [0061]
  • For producing a film with very good sealing properties it has proven advantageous for the planar orientation Δp of the film to be less than 0.168, but particularly less than 0.165. In this case the strength of the film in the direction of its thickness is so great that when the seal seam strength is measured it is specifically the seal seam which separates, and the tear does not enter the film or propagate therein. [0062]
  • The significant variables affecting the planar orientation Δp have been found to be the longitudinal and transverse stretching parameters, and also the SV (standard viscosity) of the raw material used. The processing parameters include in particular the longitudinal and transverse stretching ratios (λ[0063] MD and λTD), the longitudinal and transverse stretching temperatures (TMD and TTD), the film web speed and the nature of the stretching, in particular that in the longitudinal direction of the machine. For example, if the planar orientation Δp obtained with a machine is 0.169 with the following set of parameters: λMD=4.8 and λTD=4.0, a longitudinal stretching temperature TMD of from 80 - 118° C. and a transverse stretching temperature TTD of from 80 - 125° C., then increasing the longitudinal stretching temperature TMD to 80 - 125° C. or increasing the transverse stretching temperature TTD to 80 - 135° C., or lowering the longitudinal stretching ratio λMD to 4.3 or lowering the transverse stretching ratio λTD to 3.7 gives a planar orientation Δp within the desired range. The film web speed here was 340 m/min and the SV (standard viscosity) of the material was about 730. For the longitudinal stretching, the data mentioned are based on what is known as N-TEP stretching, composed of a low-orientation stretching step (LOE, Low Orientation Elongation) and a high-orientation stretching step (REP, Rapid Elongation Process). Other stretching systems in principle give the same ratios, but the numeric values for each process parameter may be slightly different. The temperatures given are based on the respective roll temperatures in the case of the longitudinal stretching and on infrared-measured film temperatures in the case of the transverse stretching.
  • In the heat-setting which follows, the film is held for from 0.1 to 10 s at a temperature of from 150 to 250° C. The film is then wound up in a usual manner. [0064]
  • After the biaxial stretching it is preferable for one or both surfaces of the film to be corona- or flame-treated by one of the known methods. The intensity of the treatment is generally in the range above 45 mN/m. [0065]
  • The film may also be coated in order to achieve other desired properties. Typical coatings are layers with adhesion-promoting, antistatic, slip-improving or release action. These additional layers may, it will be appreciated, be applied to the film by way of in-line coating, using aqueous dispersions, prior to the transverse stretching step. [0066]
  • Advantages of the invention: [0067]
  • The novel film has excellent sealability, very good handling properties and very good processing performance. The sealable outer layer (A) of the film seals not only with respect to itself (fin sealing) but also with respect to the nonsealable outer layer (C) (lap sealing). The minimum sealing temperature for the lap sealing here is only about 10 K higher, and the reduction in the seal seam strength is not more than 0.3 N/15 mm. [0068]
  • The gloss and haze of the film are also improved considerably. In producing the novel film it is certain that material for recycling can be refed to the extrusion process at a concentration of from 20 to 60% by weight, based on the total weight of the film, without any significant adverse effect on the physical properties of the film, in particular on its appearance. [0069]
  • The film is accordingly very useful in flexible packaging, especially where its excellent sealing properties and its good processability come in useful. This is in particular its use on high-speed packaging machines. [0070]
  • The most important film properties according to the invention can be seen again at a glance in the table below (Table 1). [0071] TABLE 1 Range according Particu- to the Pre- larly Test invention ferred preferred Unit method OUTER LAYER A Minimum <110 <105 <100 ° C. internal sealing temperature Seal seam >1.3 >1.5 >1.8 N/15 mm internal strength Average ≦40 ≦30 ≦20 nm DIN 4768, roughness Ra cut-off of 0.25 mm Range of 300-4000 500-3500 1000-3000 sec internal values measured for gas flow Gloss, 20° >120 >130 >140 DIN 67530 OUTER LAYER C COF <0.5 <0.45 <0.40 DIN 53375 Average 40 to 150 45 to 120 50 to 90 nm DIN 4768, roughness Ra cut-off of 0.25 mm Range of ≦140 ≦120 ≦100 sec internal values measured for gas flow Constants 0.29/3.00 A1/A2 and B1/B2 and 1.84/2.7 Gloss, 20° C. >140 >150 >160 DIN 67530 Other film properties Haze <4 <3 <2.5 % ASTM-D 1003-52 Planar <0.168 <0.165 <0.163 internal orientation
  • The following test methods were utilized for the purposes of the present invention to characterize the raw materials and the films: [0072]
  • SV (standard viscosity) [0073]
  • The standard viscosity SV (DCA) is measured in dichloroacetic acid by a method based on DIN 53726. [0074]
  • The intrinsic viscosity (IV) is calculated as follows from the standard viscosity[0075]
  • IV (DCA)=6.907·10−4 SV (DCA)+0.063096
  • Determination of minimum sealing temperature [0076]
  • Hot-sealed specimens (seal seam 20 mm×100 mm) are produced with a Brugger HSG/ET sealing apparatus, by sealing the film at different temperatures with the aid of two heated sealing jaws at a sealing pressure of 2 bar and with a sealing time of 0.5 s. From the sealed specimens test strips of 15 mm width were cut. The T-seal seam strength was measured as in the determination of seal seam strength. The minimum sealing temperature is the temperature at which a seal seam strength of at least 0.5 N/15 mm is achieved. [0077]
  • Seal seam strength [0078]
  • To determine the seal seam strength, two film strips of width 15 mm were placed one on top of the other and sealed at 130° C. with a sealing time of 0.5 s and a sealing pressure of 2 bar (apparatus: Brugger model NDS, single-side-heated sealing jaw). The seal seam strength was determined by the T-peel method. [0079]
  • Coefficient of friction [0080]
  • The coefficient of friction was determined to DIN 53 375. The coefficient of sliding friction was measured 14 days after production. [0081]
  • Surface tension [0082]
  • Surface tension was determined by what is known as the ink method (DIN 53 364). [0083]
  • Haze [0084]
  • The Hölz haze was measured by a method based on ASTM-D 1003-52 but, in order to utilize the most effective measurement range, measurements were made on four pieces of film laid one on top of the other, and a 1° slit diaphragm was used instead of a 4° pinhole. [0085]
  • Gloss [0086]
  • Gloss was determined to DIN 67 530. The reflectance was measured as an optical value characteristic of a film surface. Based on the standards ASTM-D 523-78 and ISO 2813, the angle of incidence was set at 20° or 60°. A beam of light hits the flat test surface at the set angle of incidence and is reflected and/or scattered thereby. A proportional electrical variable is displayed representing light rays hitting the photoelectronic detector. The value measured is dimensionless and must be stated together with the angle of incidence. [0087]
  • Determination of particle sizes on film surfaces [0088]
  • A scanning electron microscope and an image analysis system are used to determine the size distribution of elevations on film surfaces. Use is made of the XL30 CP scanning electron microscope from Philips with an integrated image analysis program: AnalySIS from Soft-Imaging System. [0089]
  • For these measurements, specimens of film are placed flat on a specimen holder. These are then metalized obliquely at an angle a with a thin metallic layer (e.g. of silver) . The symbol a here is the angle between the surface of the specimen and the direction of diffusion of the metal vapor. This oblique metalization throws a shadow behind the elevation. Since the shadows are not at this stage electrically conductive, the specimen is then further sputtered or metalized with a second metal (e.g. gold), the second coating here impacting vertically onto the surface of the specimen in such a way as not to produce any shadows in the second coating. [0090]
  • Scanning electron microscope (SEM) images are taken of the specimen surfaces prepared in this way. The shadows of the elevations are visible because of the contrast of the metallic materials. The specimen is oriented in the SEM in such as way that the shadows run parallel to one edge of the image. The following conditions are set in the SEM for recording the image: secondary electron detector, operating distance 10 mm, acceleration voltage 10 kV and spot 4.5. The brightness and contrast are set in such a way that all of the information in the image is represented as gray values and the intensity of the background noise is sufficiently small for it not to be detected as a shadow. The length of the shadows is measured by image analysis. The threshold value for shadow identification is set at the point where the second derivative of the gray value distribution of the image passes through the zero point. Before shadow identification, the image is smoothed with an N×N filter (size 3, 1 iteration). A frame is set so as to ensure that elevations which are not reproduced in their entirety in the image are not included in the measurements. The magnification, the size of the frame and the number of images evaluated are selected in such a way that a total film surface of 0.36 mm[0091] 2 is evaluated.
  • The height of the individual elevations is computed from the individual shadow lengths using the following relationship:[0092]
  • h=(tan α) * L
  • where h is the height of the elevation, α is the metalization angle and L is the shadow length. The elevations recorded in this way are classified so as to arrive at a frequency distribution. The classification is into classes of 0.05 mm width between 0 and 1 mm, the smallest class (from 0 to 0.05 mm) not being used for further evaluation calculations. The diameters (dimension perpendicular to the direction of shadow throw) of the elevations are classified in a similar way in classes of 0.2 mm width from 0 to 10 mm, and here again the smallest class is again used for further evaluation. [0093]
  • Surface gas flow time [0094]
  • The principle of the test method is based on the air flow between one side of the film and a smooth silicon wafer sheet. The air flows from the surroundings into an evacuated space, and the interface between film and silicon wafer sheet acts as a flow resistance. [0095]
  • A round specimen of film is placed on a silicon wafer sheet in the middle of which there is a hole providing the connection to the receiver. The receiver is evacuated to a pressure below 0.1 mbar. The time in seconds taken by the air to establish a pressure rise of 56 mbar in the receiver is determined. [0096]
  • Test conditions: [0097] Test area 45.1 cm2 Weight applied 1276 g Air temperature 23° C. Humidity 50% relative humidity Aggregated gas volume 1.2 cm3 Pressure difference 56 mbar
  • Determination of planar orientation Δp [0098]
  • Planar orientation is determined by measuring the refractive index with an Abbe refractometer according to internal operating prescription 24. [0099]
  • Preparation of specimens [0100]
  • Specimen size and length: from 60 to 100 mm [0101]
  • Specimen width: corresponds to prism width of 10 mm [0102]
  • To determine n[0103] MD and nα (=nz), the specimen to be tested has to be cut out from the film with the running edge of the specimen running precisely in the direction TD. To determine nTD and nα (=nz), the specimen to be tested has to be cut out from the film with the running edge of the specimen running precisely in the direction MD. The specimens are to be taken from the middle of the film web. Care must be taken that the temperature of the Abbe refractometer is 23° C. Using a glass rod, a little diiodomethane (N=1.745) or diiodomethane-bromo-naphthalene mixture is applied to the lower prism, which has been cleaned thoroughly before the test. The refractive index of the mixture must be greater than 1.685. The specimen cut out in the direction TD is firstly laid on top of this, in such a way that the entire surface of the prism is covered. Using a paper wipe the film is now firmly pressed flat onto the prism, so that it is firmly and smoothly positioned thereon. The excess liquid must be sucked away. A little of the test liquid is then dropped onto the film. The second prism is swung down and into place and pressed firmly into contact. The right-hand knurled screw is then used to turn the indicator scale until a transition from light to dark can be seen in the field of view in the range from 1.62 to 1.68. If the transition from light to dark is not sharp, the colors are brought together using the upper knurled screw in such a way that only one light and one dark zone are visible. The sharp transition line is brought to the crossing point of the two diagonal lines (in the eyepiece) using the lower knurled screw. The value now indicated on the measurement scale is read off and entered into the test record. This is the refractive index nMD in the machine direction. The scale is now turned using the lower knurled screw until the range visible in the eyepiece is from 1.49 to 1.50.
  • The refractive index n[0104] α or nz (in the direction of the thickness of the film) is then determined. To improve the visibility of the transition, which is only weakly visible, a polarization film is placed over the eyepiece. This is turned until the transition is clearly visible. The same considerations apply as in the determination of nMD. If the transition from light to dark is not sharp (colored), the colors are brought together using the upper knurled screw in such a way that a sharp transition can be seen. This sharp transition line is brought into the crossing point of the two diagonal lines using the lower knurled screw, and the value indicated on the scale is read off and entered into the table.
  • The specimen is then turned, and the corresponding refractive indices n[0105] MD and nα (=nz) of the other side are measured and entered into an appropriate table.
  • After determining the refractive indices in, respectively, the direction MD and the direction of the thickness of the film, the specimen strip cut out in the direction MD is placed in position and the refractive indices n[0106] TD and nα (=nz) are determined accordingly. The strip is turned over, and the values for the B side are measured. The values for the A side and the B side are combined to give average refractive indices. The orientation values are then calculated from the refractive indices using the following formulae:
  • Δn=n MD −n TD
  • Δp=(n MD +n TD)/2−n z
  • n av=(n MD +n TD +n z)/3
  • EXAMPLE 1
  • Chips made from polyethylene terephthalate (prepared by the transesterification process with Mn as transesterification catalyst, Mn concentration: 100 ppm) were dried at 150° C. to residual moisture below 100 ppm and fed to the extruder for the base layer (B) . Chips made from polyethylene terephthalate and a filler were likewise fed to the extruder for the nonsealable outer layer (C). [0107]
  • Alongside this, chips were prepared made from a linear polyester which is composed of an amorphous copolyester with 78 mol % of ethylene terephthalate and 22 mol % of ethylene isophthalate (prepared via the transesterification process with Mn as transesterification catalyst, Mn concentration: 100 ppm). The copolyester was dried at a temperature of 100° C. to a residual moisture below 200 ppm and fed to the extruder for the sealable outer layer (A). [0108]
  • Coextrusion followed by stepwise longitudinal and transverse orientation was then used to produce a transparent, three-layer film with ABC structure and with a total thickness of 12 μm. The thickness of each outer layer can be seen in Table 2. [0109] Outer layer (A), a mixture made from: 97.0% by weight of copolyester with an SV of 800 3.0% by weight of masterbatch made from 97.75% by weight of copolyester (SV of 800) and 1.0% by weight of ® Sylobloc 44 H (synthetic SiO2 from Grace) and 1.25% by weight of ® Aerosil TT 600 (pyrogenic SiO2 from Degussa) Base layer (B): 100.0% by weight of polyethylene terephthalate with an SV of 800 Outer layer (C), a mixture made from: 88% by weight of polyethylene terephthalate with an SV of 800 12% by weight of masterbatch made from 97.75% by weight of copolyester (SV of 800) and 1.0% by weight of Sylobloc 44 H (synthetic SiO2 from Grace) and 1.25% by weight of Aerosil TT 600 (chain- type SiO2 from Degussa) The production conditions in each process step were: Extrusion: Temperatures Layer A: 3e+08 ° C. Layer B: ° C. Layer C: ° C. Die width: 2.5 mm Take-off roll 30° C. temperature Longitudinal Temperature: 80-125° C. stretching: Longitudinal stretching 4.2 ratio: Transverse Temperature: 80-135° C. stretching: Transverse stretching 4 ratio Heat-setting: Temperature: 230° C. Duration: 3 s
  • The film had the required good sealing properties and the required handling, and the required processing performance. Tables 2 and 3 show the structure of the films and the properties achieved in films produced in this way. [0110]
  • EXAMPLE 2
  • As Example 1, except that the outer layer thickness for the sealable layer (A) was raised from 1.5 to 2.0 μm, with otherwise identical film structure and an identical method of production. This gives an improvement in the sealing properties, and in particular the seal seam strength improves markedly. [0111]
  • EXAMPLE 3
  • As Example 1, except that a film of 20 μm thickness was produced. The outer layer thickness for the sealable layer (A) was 2.5 μm and the thickness for the nonsealable layer (C) was 2.0 μm. This again improves the sealing properties, and in particular the seal seam strength improves markedly. Again, there has been a slight improvement in the handling of the film. [0112]
  • EXAMPLE 4
  • As Example 3, except that the copolymer for the sealable outer layer (A) was changed. Instead of the amorphous copolyester having 78 mol % of polyethylene terephthalate and 22 mol % of ethylene isophthalate, use was made of an amorphous copolyester having 70 mol % of polyethylene terephthalate and 30 mol % of ethylene isophthalate. The polymer was processed on a vented twin-screw extruder but did not have to be predried. The outer layer thickness for the sealable layer (A) was again 2.5 μm, and the thickness of the nonsealable layer (C) was 2.0 μm. This improved the sealing properties, and in particular there was a marked improvement in the seal seam strength. To achieve good handling and good processing performance from the film, the pigment concentration in the two outer layers was slightly raised. [0113]
  • COMPARATIVE EXAMPLE 1
  • As Example 1, except that the sealable outer layer (A) was unpigmented. Although this has improved the sealing properties somewhat, the handling of the film and its processing performance have deteriorated unacceptably. [0114]
  • COMPARATIVE EXAMPLE 2
  • As Example 1, except that the sealable outer layer (A) had the same pigmentation level as the nonsealable outer layer (C). This measure has improved the handling and the processing properties of the film, however the sealing properties have become markedly poorer. [0115]
  • COMPARATIVE EXAMPLE 3
  • As Example 1, except that the nonsealable outer layer (A) was given markedly less pigmentation. The handling and processing performance of the film has become markedly poorer. [0116]
  • COMPARATIVE EXAMPLE 4
  • Example 1 from EP-A-0 035 835 was repeated. The sealing performance of the film, its handling properties and its processing performance are poorer than in the examples according to the invention. [0117] TABLE 2 Film Layer thicknesses Average pigment diameter Pigment concentrations thickness Film μm Pigments in layers in layers μm ppm Example μm structure A B C A B C A B C A B C E 1 12 ABC 1.5 9 1.5 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 300 0 1200 Aerosil TT 600 Aerosil TT 600 0.04 0.04 375 1500 E 2 12 ABC 2 8.5 1.5 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 300 0 1200 Aerosil TT 600 Aerosil TT 600 0.04 0.04 375 1500 E 3 20 ABC 2.5 15.5 2 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 300 0 1200 Aerosil TT 600 Aerosil TT 600 0.04 0.04 375 1500 E 4 20 ABC 2.5 15.5 2 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 400 0 1500 Aerosil TT 60 Aerosil TT 600 0.04 0.04 500 1875 CE 1 12 ABC 1.5 9 1.5 none none Sylobloc 44 H 2.5 0 1200 Aerosil TT 600 0.04 1500 CE 2 12 ABC 1.5 9 1.5 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 300 0 1200 Aerosil TT 600 Aerosil TT 600 0.04 0.04 375 1500 CE 3 12 ABC 1.5 9 1.5 Sylobloc 44 H none Sylobloc 44 H 2.5 2.5 300 0  600 Aerosil TT 600 Aerosil TT 600 0.04 0.04 375  750 CE 4 15 AB 2.25 12.8 Gasil 35 none 3 2500  0
  • [0118] TABLE 3 Minimum Coeffi- sealing cient of temperature Seal seam friction Average Winding ° C. strength COF roughness Values perform- A side A side C side Ra measured for ance and Process- Ex- with with with nm gas flow Constants Gloss handling ing am- respect respect respect A C A C A/B A C proper- perform- ple to A side to A side to C side side side side side A C Δp side side Haze ties ance E 1 100 2.0 0.45 25 65 1200 120 0.5 3.1 0.17 140 170 2.5 ++ ++ E 2  98 2.7 0.45 26 65 1280 120 0.5 3.1 0.17 140 170 2.5 ++ ++ E 3  95 3 0.41 23 61 1110 120 0.5 3.1 0.17 130 170 3 ++ ++ E 4  85 3.3 0.4  23 65 1300 110 0.5 3.1 0.17 130 170 3 ++ ++ CE 1  98 2.1 0.45 10 65 10,000  80 0.17 160 170 1.5 CE 2 110 1 0.45 65 65  80  80 0.17 130 170 2.8 CE 3 100 2 0.45 25 37 1200 150 0.17 160 190 1.5 CE 4 115 0.97 >2 70 20  50 >5000 12

Claims (11)

What is claimed is:
1. A coextruded, biaxially oriented, sealable polyester film with at least a base layer (B), with a sealable outer layer (A) arranged on outside of the base layer (B) and with another outer layer (C) arranged on the other side of the base layer (B), where the sealable outer layer (A) has a minimum sealing temperature of not more than about 110° C. and a seal seam strength of at least about 1.3 N/15 mm of film width, wherein the sealable outer layer (A) has an average surface roughness, expressed as Ra, of ≦40 nm, and has a value measured for gas flow within the range from about 300 to about 4000 s, wherein the nonsealable outer layer (C) has a coefficient of friction COF of≦0.5, an average surface roughness, expressed as Ra, within the range of 40≦Ra≦150 nm, and a value measured for gas flow of ≦140 s, and wherein, for the nonsealable outer layer (C), the number of elevations Nc per mm2 of film surface is correlated with their respective heights h via the following equations:
A c1 −B c1·log h/μm<log N c /mm 2 <A c2 −B c2·log h/μm
where
0.01 μm≦h≦10 μm
and
A c1=0.29, B c1=3.30
and
A c2=1.84, B c2=2.70.
2. The sealable polyester film as claimed in
claim 1
, wherein the sealable outer layer (A) comprises an amorphous copolyester composed of ethylene terephthalate units and of ethylene isophthalate units and of ethylene glycol units.
3. The sealable polyester film as claimed in
claim 1
, wherein the amorphous copolyester of the sealable outer layer (A) comprises from about 40 to about 95 mol % of ethylene terephthalate and from about 60 to about 5 mol % of ethylene isophthalate.
4. The sealable polyester film as claimed in
claim 1
, wherein the sealable outer layer (A) has a thickness in the range from about 0.2 to about 3 μm.
5. The sealable polyester film as claimed in
claim 1
, which comprises antiblocking agents selected from the group consisting of inorganic and organic particles and mixtures of these.
6. The sealable polyester film as claimed in
claim 5
, which comprises, as antiblocking agent, particles with an average primary particle diameter below about 100 nm, measured by the sedigraph method, or particles with an average primary particle diameter greater than or equal to about 1 W, or particles with an average primary particle diameter below about 100 nm measured by the sedigraph method and particles with an average primary particle diameter≧about 1 μm.
7. The sealable polyester film as claimed in
claim 6
, wherein the amount of particles in the base layer (B) is within the range from about 0 to about 0.15% by weight, wherein the amount of particles in the nonsealable outer layer (C) is within the range from about 0.1 to about 1.0% by weight, and wherein the sealable outer layer (A) has an amount of particles within the range from about 0.01 to about 0.2% by weight, all data being based on % by weight and on the total weight of the respective layer.
8. The sealable polyester film as claimed in
claim 1
, wherein the thicknesses of the outer layers (A) and (C) are above about 0.1 μm the thicknesses of the outer layers (A) and (C) being identical or different.
9. The sealable polyester film as claimed in
claim 1
, wherein the total thickness of the polyester film is within the range from about 3 to about 80 μm, the base layer (B) making up a proportion of from about 5 to about 90% of the total thickness.
10. A process for producing a sealable polyester film as claimed in
claim 1
, in which the polymers for the base layer (B) and the two outer layers (A) and (C) are fed to separate extruders, the melts are then coextruded through a coextrusion die to give a flat melt film and then the film is drawn off with the aid of a chill roll and solidified, and then biaxially stretch-oriented and heat-set, and then, where appropriate, corona- or flame-treated on at least one surface, which process comprises carrying out the biaxial stretching in succession, first stretching longitudinally (in the machine direction) and then transversely (perpendicularly to the machine direction), carrying out the longitudinal stretching at a temperature within the range from about 80 to about 130° C., and the transverse stretching within the range from about 90 to about 150° C., and setting the longitudinal stretching ratio within the range from about 2.5:1 to about 6:1, and the transverse stretching ratio within the range from about 3.0:1 to about 5.0:1.
11. The process as claimed in
claim 10
, wherein one or both surfaces of the film are in-line coated after the longitudinal stretching and prior to the transverse stretching.
US09/818,878 2000-03-29 2001-03-27 Sealable, biaxially oriented polyester film Expired - Fee Related US6423401B2 (en)

Priority Applications (3)

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DE10015633 2000-03-29

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US6423401B2 (en) 2002-07-23
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JP2001322220A (en) 2001-11-20
EP1138480A3 (en) 2004-01-14
EP1138480B1 (en) 2009-08-12
EP1138480A2 (en) 2001-10-04
KR100775606B1 (en) 2007-11-13

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