WO1995009728A1 - Controlled-porosity, calendered spunbonded/melt blown laminates - Google Patents

Controlled-porosity, calendered spunbonded/melt blown laminates Download PDF

Info

Publication number
WO1995009728A1
WO1995009728A1 PCT/US1994/010592 US9410592W WO9509728A1 WO 1995009728 A1 WO1995009728 A1 WO 1995009728A1 US 9410592 W US9410592 W US 9410592W WO 9509728 A1 WO9509728 A1 WO 9509728A1
Authority
WO
WIPO (PCT)
Prior art keywords
melt
sheet
spunbonded
blown
composite sheet
Prior art date
Application number
PCT/US1994/010592
Other languages
French (fr)
Inventor
Hyun Sung Lim
Hyunkook Shin
Original Assignee
E.I. Du Pont De Nemours And Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by E.I. Du Pont De Nemours And Company filed Critical E.I. Du Pont De Nemours And Company
Priority to JP51082595A priority Critical patent/JP3615549B2/en
Priority to KR1019960701735A priority patent/KR100323177B1/en
Priority to DE69402561T priority patent/DE69402561T2/en
Priority to CA002173327A priority patent/CA2173327C/en
Priority to EP94929843A priority patent/EP0722389B1/en
Publication of WO1995009728A1 publication Critical patent/WO1995009728A1/en

Links

Classifications

    • 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
    • B32B5/22Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
    • B32B5/24Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
    • B32B5/26Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
    • 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
    • B32B37/06Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the heating method
    • 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
    • B32B5/02Layered 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 structural features of a fibrous or filamentary layer
    • B32B5/024Woven fabric
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/54Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
    • D04H1/559Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving the fibres being within layered webs
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/54Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
    • D04H1/56Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving in association with fibre formation, e.g. immediately following extrusion of staple fibres
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H13/00Other non-woven fabrics
    • 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
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/02Synthetic macromolecular fibres
    • B32B2262/0253Polyolefin fibres
    • 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
    • B32B2307/582Tearability
    • B32B2307/5825Tear resistant
    • 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
    • B32B2307/714Inert, i.e. inert to chemical degradation, corrosion
    • B32B2307/7145Rot proof, resistant to bacteria, mildew, mould, fungi
    • 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
    • B32B2307/724Permeability to gases, adsorption
    • 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
    • B32B2307/726Permeability to liquids, absorption
    • B32B2307/7265Non-permeable
    • 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
    • B32B2439/00Containers; Receptacles
    • B32B2439/80Medical packaging
    • 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
    • Y10S428/903Microfiber, less than 100 micron diameter
    • 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
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/608Including strand or fiber material which is of specific structural definition
    • Y10T442/614Strand or fiber material specified as having microdimensions [i.e., microfiber]
    • Y10T442/62Including another chemically different microfiber in a separate layer
    • 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
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/659Including an additional nonwoven fabric
    • Y10T442/66Additional nonwoven fabric is a spun-bonded fabric

Definitions

  • This invention relates to calendered laminates of spunbonded and melt-blown polypropylene webs which combine high opacity with low air and water permeability but good moisture vapor transmission, and good barrier properties against bacteria.
  • Spunbonded polyethylene sheet (prepared from flash-spun polyethylene plexifilamentary web) has been used for some years as an air flow resistant "housewrap", as well as in sterile packaging applications.
  • the sheet is known for its strength, durability, opacity and ability to reduce air penetration, yet maintains a high moisture vapor transmission rate and, in addition, provides excellent barrier to bacteria.
  • a housewrap product with higher tear resistance, especially in areas exposed to strong winds.
  • sterile packaging for a higher melting material, capable of withstanding steam sterilization.
  • One polyolefin material that has sufficiently high melting temperature and excellent mechanical properties is polypropylene.
  • U.S. Patent 4,898,761 to Dunaway et al. discloses a barrier housewrap fabric impermeable to liquid and permeable to water vapor, which is made by laminating an impermeable polymer film to a polypropylene sheet available, La., from E. I. du Pont de Nemours and Company under the trademark TYPAR® and needling the resultant sheet with fine diameter needles to make the sheet porous.
  • U.S. Patent 4,898,761 to Dunaway et al. (Reemay Inc.) discloses a barrier housewrap fabric impermeable to liquid and permeable to water vapor, which is made by laminating an impermeable polymer film to a polypropylene sheet available, La., from E. I. du Pont de Nemours and Company under the trademark TYPAR® and needling the resultant sheet with fine diameter needles to make the sheet porous.
  • U.S. Patent 4,898,761 to Dunaway et al. discloses
  • Patent 4,684,568 to Lou describes a water vapor-permeable, liquid water-impermeable fabric made by applying a coating of polypropylene film to a TYPAR® sheet and then calendering. Although these products have adequate tear resistance and strength, they do not have a good balance of air penetration resistance and moisture- vapor transmission rate.
  • U.S. Patent 4,900,619 to Ostrowski et al. (James River Corp.) describes a translucent nonwoven composite of thermoplastic melt- blown and spunbonded webs laminated together by hot-calendering in a nip made by a smooth, heated steel roll and a resilient roll heated with an external, infrared source, each roll being at a temperature of about 116- 160°C.
  • the thermoplastic material in each layer is polypropylene.
  • translucent is understood to mean “permitting the passage of light”.
  • the degree of translucency can be determined, e.g., by an opacity measurement (TAPPI test method T 425 om-86, "Opacity of Paper”). By that test, the commercial James River product has an opacity of less than 50%. It is possible that this low opacity results from laminating the sheets between two heated calender rolls, forming a film.
  • translucency indicates the occurrence of permanent changes of certain physical properties of the fibers or of their distribution in the sheet, which could lead to lower mechanical integrity or tensile strength.
  • a process for forming the above composite sheet by calendering an assembly consisting of a melt-blown polypropylene web and at least one spunbonded sheet in a calender comprising a smooth metal roll heated to a temperature of 140-170°C, operating against an unheated, resilient roll, at a nip loading of about 1.75x10- 5 -3.5x10- 5 N/m; with the proviso that when forming a two-layer composite sheet, only the melt-blown fiber web is in direct contact with the heated metal roll; and when forming a three-layer composite sheet, the spunbonded sheet in contact with the heated metal roll is made of filaments having a dtex-per- filament (DTPF) value of less than 6.
  • DTPF dtex-per- filament
  • Fig. 2 is a schematic drawing representing the process of calendering a three-layer composite sheet.
  • melt-blown polypropylene fiber and spunbonded polypropylene fiber are well known and commercially available.
  • Melt- blown polypropylene fibers can be made by extruding the polymeric material into fine streams and stretching those streams into fibers of small diameter by exposure to high velocity heated air, as described in U.S. Patent 3,978,185 (to Buntin et al).
  • Those fibers, with an average diameter of about 1-10 ⁇ m, are collected in the form of a web on a moving belt.
  • the web may be either electrostatically charged or uncharged.
  • the charging process is described in U.S. Patent 4,904,174 (to Moosmayer et al. )
  • Polypropylene suitable for making melt-blown fibers has a rather high melt flow rate of about 200-800 dg/min.
  • Spunbonded polypropylene fibers can be made by any convenient process, for example, by melt-spinning the polymer in a generally known manner, e.g., as described in U.S. Patents 3,821,062 to Henderson; 3,563,838 to Edwards; and 3,338,992 to Kinney.
  • the spunbonded fibers are long and have an average diameter of at least 20 ⁇ m.
  • the polypropylene resin used for making this spunbonded filament have a melt flow rate of about 3.5-4.6 dg/min.
  • the resin used for manufacturing TYPAR® has a melt flow rate of 4.2 dg/min, and the fibers have a DTPF of greater than 9.
  • the spunbonded layer in the composites of the present invention provides mechanical strength and integrity, while the melt- blown layer provides the desired microporosity and barrier properties.
  • the composites of the present invention can be either simple laminates consisting of one layer of melt-blown web laminated to one layer of spunbonded web or can be in the form of a three-layer sandwich, in which the melt-blown web forms the core, while the spunbonded web forms the outer layers.
  • Calendering reduces the web's porosity and imparts to it its desirable barrier properties.
  • This operation can be carried out in a standard apparatus comprising a heated metal, ususally steel, roll and an unheated resilient roll, wnich can be made of any suitable material, such as, e.g., densely packed cotton, wool, or polyamide. Typical Shore D hardness of the resilient material can be about 75-85.
  • the hardness of the unheated resilient roll determines the "footprint", i.e., the instant area being calendered. If the hardness is reduced, contact area is increased and the pressure decreases; if the hardness is increased, the contact area is decreased and the pressure increases.
  • a balance of pressure and temperature is sought to produce the desired calendering conditions for controlling the porosity of the resulting composite sheet. Calendering with only one heated roll increases opacity. By contrast, when both rolls are heated, the resulting sheet is translucent and more film- or paper-like, which is undesirable. Translucent, paper-like sheet often exhibits lower tensile strength but also especially lower tear strength This can be attributed to a significantly decreased contribution of individual fibers and significant loss of fiber orientation.
  • the preferred heated roll temperature according to the present invention is 140-155°C.
  • the degree of porosity of the web depends, among others, on nip loading, which is the ratio of force applied to the sheet in the nip of the calender to the width of the sheet; the higher the nip loading the lower the porosity.
  • nip loading should be about 1.75-3.50x10" 5 N/m.
  • melt-blown polypropylene fiber web When forming a two-layer composite, the melt-blown polypropylene fiber web directly contacts the heated metal roll. This permits operation at a temperature lower than the melting point of polypropylene, although any temperature up to about 170°C can be used in principle.
  • the adhesion of the spunbonded sheet not in contact with the heated metal roll can be further improved be preheating the sheet before the calendering step, for example, by contacting it with another metal roll heated to a temperature of about 20°C below the operating temperature of the metal calender roll.
  • Fig. 1 schematically illustrates the process of the present invention for making a two-layer composite, wherein 10 is the spunbonded sheet component, and 20 is the melt-blown web component; 1 is the heated metal roll, and 2 is the unheated resilient roll.
  • the arrows show the direction of movement of the components and of the composite as well as the direction of rotation of the rolls.
  • Fig. 2 schematically illustrates the process of the present invention for making a three-layer composite, wherein 30 and 40 are the spunbonded sheet components, and 50 is the melt-blown web component; 3 is the heated metal roll, and 4 is the unheated resilient roll.
  • the arrows show the direction of movement of the components and of the composite as well as the direction of rotation of the rolls.
  • the composite For use as a housewrap, the composite should have under standard temperature and pressure conditions a Gurley-Hill porosity of 30-75 seconds. Its water vapor transmission rate desirably should be at least 500 g/m 2 in 24 hours or more. Liquid water permeability should be low. This property is normally evaluated by measuring the hydrostatic head pressure under standard conditions. Preferably, the hydrostatic head pressure should be at least 0.9 m. The tensile strength should be at least 3000 N per meter of width.
  • the Gurley-Hill porosity of the composite sheet should be 5-50 seconds.
  • the composite sheet desirably should under standardized test conditions (to be described below) provide an effective barrier such that at least 60% of the test samples show no bacteria present.
  • the tensile strength should be at least 1000 N per meter of width.
  • Materials with a Gurley-Hill porosity of about 5-75 seconds have sometimes been used in the past for microfiltration of liquids. See, for example Lim et al, TYVEKfor Microfiltration Media, Fluid/Particle Separation Journal, Vol. 2, No. 1, March, 1989.
  • Microfiltration elements can also be made from the composite sheets of the present invention.
  • Gurley-Hill porosity - TAPPI 1 T-460 om-86 This test measures the time required for 100 cm ⁇ of air to pass through a sample under standard conditions.
  • Hydrostatic head - AATCC 2 Test Method 127-1985 The specimen is mounted under the orifice of a conical well and subjected to a steadily increasing water pressure, until three points of leakage appear on its undersurface.
  • Bacteria barrier property A bacterial test chamber (BTC), designed to hold several samples, has been devised by the DuPont Compay. A cloud of bacteria spores generated by a nebulizer is delivered
  • fibers of the spunbonded sheets had a diameter of 20 ⁇ m, and the fibers of the melt-blown webs had an average diameter of 1-10 ⁇ m.
  • Example 1 Two-layer composite for housewrap application The spunbonded polypropylene sheet was DUPONT's
  • the melt-blown web used in this Example was made by extruding molten polypropylene through a spinneret and fibrillating the extruded fibers at the spinneret with high temperature and high velocity air streams to form microfibers.
  • the melt-blown fibers were formed into a sheet on a moving belt equipped with a suction box.
  • the melt-blowing technology is being licensed for commercial use by Exxon Chemical Co.
  • the spunbonded polypropylene sheet and the melt-blown web were laminated by calendering in the nip formed between a smooth metal roll and a polyamide roll, which had a Shore D hardness of 78.
  • the metal roll was heated to a surface temperature of 154°C.
  • the polyamide roll was not heated.
  • a load of 2.75xl0"5 N/m was applied to the sheet/web assembly as it advanced through the calender nip at a speed of 20 m per minute.
  • the melt-blown web contacted the steel heated roll while the spunbonded sheet contacted the polyamide roll. Under these conditions, excellent adhesion between the spunbonded sheet and the melt-blown web was obtained.
  • the resulting composite sheet exhibited high air flow resistance and high water vapor transmission rate properties. In addition, high tensile and tear strengths also were demonstrated.
  • the physical properties of both starting webs as well as of the laminated composite sheet are given below in Table 1.
  • This example illustrates the range of air permeabilities that can be obtained by varying the nip loading and speed, at a constant temperature of 155°C.
  • the spunbonded sheet was TYPAR® having a basis weight of 68 g/m 2
  • the melt-blown polypropylene web had a basis weight of 38 g/m 2 .
  • Table 3 The experimental conditions and results are presented in Table 3, below.
  • Example 3 Three-layer composite sheet for sterile packaging applications.
  • the composite had a core of melt-blown polypropylene fiber web and outer layers of spunbonded polypropylene sheets, where the spunbonded sheets were not TYPAR® but were made with filaments having a DTPF value of less than 6.
  • the composite sheet formed a good barrier to bacteria and could be sterilized with steam.
  • the spunbonded web was made by extruding molten polypropylene through multiple spinneret orifices.
  • the resulting filaments were quenched with controlled temperature air and suction fed through a venturi jet to a distribution chamber to ensure the fanning and entangling of the filaments.
  • the entangled filaments were deposited as a random web on a moving belt, which had a suction box under it.
  • the melt-blown web used in this Example was prepared as in Example 1.
  • the two spunbonded outer layers and the melt-blown inner layer were laminated in the nip of a calender between a smooth metal roll and a cotton-filled roll having a Shore D hardness of 80-83.
  • the metal roll was heated to a surface temperature of 149°C, while the cotton-filled roll was unheated.
  • a load of 1.75x10" ⁇ N/m was applied to the sheet as the sheet advanced through the calender nip at a speed of 59.4 m/min.
  • Table 4 The physical properties of the individual components as well as of the composite sheet are given in Table 4. It can be seen that air permeability of the composite was significantly lower, with higher hydrostatic head, than that of either the melt-blown web or the spunbonded sheet.
  • Example 4 Additional composites for sterile packaging
  • This example illustrates the range of permeability and bacteria barrier properties that can be achieved by use of the process of the present invention.
  • the nip loading was varied, while the calendering temperature was held constant at 143°C, and calendering speed was held constant at 59.4 m/min.
  • the calendering temperature was varied, while the nip loading was held constant at 1.75xl0 ⁇ 5 N/m, and the calendering speed was held constant at 59.4 m/min.
  • the physical properties of the composite sheets from these two series of runs are shown, respectively, in Tables 5 and 6, below.
  • This example illustrates a further improvement in the bacteria barrier property when an electrostatically charged melt-blown web is used as the inner layer of a three-layer composite of this invention.
  • the melt-blown fibers are electrostatically charged in the web-forming step, e.g., as described in U.S. Patents 4,215,682 to Kubik et. al. (3M Company) and 4,904,174 to Mossmeyer (Exxon Company and Battelle Institute).
  • the composite was made substantially as described in Example 3. The results are shown in Table 7, below.

Abstract

Controlled porosity composite sheets comprising a melt-blown polypropylene fiber web (20) having a spunbonded polypropylene fiber sheet (10) laminated to at least one side thereof are made by calendering an assembly of the component webs in such a manner that, when a two-layer composite sheet is made, the web of melt-blown fibers is in contact with a metal roll (1) heated to 140-170 °C operating against an unheated resilient roll (2) and, when a three-layer composite sheet is made, the spunbonded web in contact with the heated metal roll has a dtex per fiber value of less than 6. These composite sheets have a Gurley-Hill porosity of about 5-75 seconds, excellent mechanical and tear strengths, high water vapor penetration rate, and low liquid water permeability. They are particularly suitable for making housewrap sheets and sheets for sterile packaging. In the sterile packaging field, they are significantly better than medical paper used for the same purpose.

Description

TITLE CONTROLLED-POROSITY, CALENDERED SPUNBONDED/MELT
BLOWN LAMINATES BACKGROUND OF THE INVENTION This invention relates to calendered laminates of spunbonded and melt-blown polypropylene webs which combine high opacity with low air and water permeability but good moisture vapor transmission, and good barrier properties against bacteria.
Spunbonded polyethylene sheet (prepared from flash-spun polyethylene plexifilamentary web) has been used for some years as an air flow resistant "housewrap", as well as in sterile packaging applications. The sheet is known for its strength, durability, opacity and ability to reduce air penetration, yet maintains a high moisture vapor transmission rate and, in addition, provides excellent barrier to bacteria. However, there exists a need for a housewrap product with higher tear resistance, especially in areas exposed to strong winds. At the same time, there is a need in sterile packaging for a higher melting material, capable of withstanding steam sterilization. One polyolefin material that has sufficiently high melting temperature and excellent mechanical properties is polypropylene.
Use of polypropylene housewrap sheets is known. Thus, U.S. Patent 4,898,761 to Dunaway et al. (Reemay Inc.) discloses a barrier housewrap fabric impermeable to liquid and permeable to water vapor, which is made by laminating an impermeable polymer film to a polypropylene sheet available, La., from E. I. du Pont de Nemours and Company under the trademark TYPAR® and needling the resultant sheet with fine diameter needles to make the sheet porous. U.S. Patent 4,684,568 to Lou (DuPont) describes a water vapor-permeable, liquid water-impermeable fabric made by applying a coating of polypropylene film to a TYPAR® sheet and then calendering. Although these products have adequate tear resistance and strength, they do not have a good balance of air penetration resistance and moisture- vapor transmission rate.
US 4,766,029 to Brock et al. (Kimberley-Clark Corp.) discloses a housewrap which is a calendered, three-layer laminate of spunbonded/melt-blown/spunbonded webs. The melt-blown layer has two components, namely, polyethylene and polypropylene microfibers. During lamination, polyethylene fibers melt and the material flows, to close up the interstitial space and to bond the layers together. This creates a semi-permeable laminate. The requirement of two types of fibers in the melt-blown material is on obvious disadvantage.
U.S. Patent 4,900,619 to Ostrowski et al. (James River Corp.) describes a translucent nonwoven composite of thermoplastic melt- blown and spunbonded webs laminated together by hot-calendering in a nip made by a smooth, heated steel roll and a resilient roll heated with an external, infrared source, each roll being at a temperature of about 116- 160°C. Typically, the thermoplastic material in each layer is polypropylene.
The term "translucent" is understood to mean "permitting the passage of light". The degree of translucency can be determined, e.g., by an opacity measurement (TAPPI test method T 425 om-86, "Opacity of Paper"). By that test, the commercial James River product has an opacity of less than 50%. It is possible that this low opacity results from laminating the sheets between two heated calender rolls, forming a film. Usually, translucency indicates the occurrence of permanent changes of certain physical properties of the fibers or of their distribution in the sheet, which could lead to lower mechanical integrity or tensile strength. Further, it is preferred, for aesthetic reasons, to have a housewrap that is opaque, rather than translucent. Even though the housewrap eventually is covered by a siding, a house under construction covered with a housewrap through which all the studs and joints can be seen appears unsightly.
International Application WO 87/05952 of Kimberley-Clark discloses impregnation of spunbonded filaments with a fluorocarbon prior to calendering . The product is a spunbonded/melt- blown/spunbonded nonwoven laminate for disposable garments. The purpose of calendering is to improve the resistance of the laminated garment's surface to "fuzzing and linting", while maintaining porosity, softness and drape. Without fluorocarbon impregnation, garments lose their porosity during calendering. The calender comprises a smooth steel roll heated to the melting temperature of the fibers in the layer in contact therewith (e.g,167°C for polypropylene) and an unheated roll which can be made of such materials as plastic, cotton, or paper.
There is a need for a strong, opaque web with good water vapor penetration rate, low air permeability, no liquid water permeability, and good barrier properties against bacteria.
SUMMARY OF THE INVENTION According to the present invention, there is now provided a high-strength, tear-resistant, calendered, composite sheet having an opacity, as determined by TAPPI test T-519 om-86, of at least 75%, low air permeability expressed as Gurley-Hill porosity of 5-75 seconds, high water vapor transmission rate of at least 500 g/m.2 in 24 hours according to ASTM standard E96, method B, low liquid water permeability expressed by a hydrostatic head pressure of at least 0.75 m according to AATCC standardl27-1985, and barrier properties against bacteria that are significantly better than those of medical paper used for sterile packaging, which sheet comprises one melt-blown polypropylene fiber web and a spunbonded polypropylene fiber sheet laminated to at least one side thereof, the melt-blown fibers having an average diameter of 1-10 mm, the melt-blown fiber web itself having an average weight of about 17-40.7 g/m.2, and the fibers of the spunbonded sheet having an average diameter of at least 20 mm, the spunbonded sheet itself having an average weight of about 17-100 g/m2.
There also is provided a process for forming the above composite sheet by calendering an assembly consisting of a melt-blown polypropylene web and at least one spunbonded sheet in a calender comprising a smooth metal roll heated to a temperature of 140-170°C, operating against an unheated, resilient roll, at a nip loading of about 1.75x10-5-3.5x10-5 N/m; with the proviso that when forming a two-layer composite sheet, only the melt-blown fiber web is in direct contact with the heated metal roll; and when forming a three-layer composite sheet, the spunbonded sheet in contact with the heated metal roll is made of filaments having a dtex-per- filament (DTPF) value of less than 6. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic drawing representing the process of calendering a two-layer composite sheet.
Fig. 2 is a schematic drawing representing the process of calendering a three-layer composite sheet.
DETAILED DESCRIPTION OF THE TNVRNTTON Both melt-blown polypropylene fiber and spunbonded polypropylene fiber are well known and commercially available. Melt- blown polypropylene fibers can be made by extruding the polymeric material into fine streams and stretching those streams into fibers of small diameter by exposure to high velocity heated air, as described in U.S. Patent 3,978,185 (to Buntin et al). Those fibers, with an average diameter of about 1-10 μm, are collected in the form of a web on a moving belt. The web may be either electrostatically charged or uncharged. The charging process is described in U.S. Patent 4,904,174 (to Moosmayer et al. ) Polypropylene suitable for making melt-blown fibers has a rather high melt flow rate of about 200-800 dg/min.
Spunbonded polypropylene fibers can be made by any convenient process, for example, by melt-spinning the polymer in a generally known manner, e.g., as described in U.S. Patents 3,821,062 to Henderson; 3,563,838 to Edwards; and 3,338,992 to Kinney. The spunbonded fibers are long and have an average diameter of at least 20 μm. When forming a two-layer composite, it is preferred to employ a spunbonded sheet in which the fibers have a DTPF value of about 10 or more. The polypropylene resin used for making this spunbonded filament have a melt flow rate of about 3.5-4.6 dg/min. The resin used for manufacturing TYPAR® has a melt flow rate of 4.2 dg/min, and the fibers have a DTPF of greater than 9.
The spunbonded layer in the composites of the present invention provides mechanical strength and integrity, while the melt- blown layer provides the desired microporosity and barrier properties. The composites of the present invention can be either simple laminates consisting of one layer of melt-blown web laminated to one layer of spunbonded web or can be in the form of a three-layer sandwich, in which the melt-blown web forms the core, while the spunbonded web forms the outer layers.
Calendering reduces the web's porosity and imparts to it its desirable barrier properties. This operation can be carried out in a standard apparatus comprising a heated metal, ususally steel, roll and an unheated resilient roll, wnich can be made of any suitable material, such as, e.g., densely packed cotton, wool, or polyamide. Typical Shore D hardness of the resilient material can be about 75-85. The hardness of the unheated resilient roll determines the "footprint", i.e., the instant area being calendered. If the hardness is reduced, contact area is increased and the pressure decreases; if the hardness is increased, the contact area is decreased and the pressure increases. A balance of pressure and temperature is sought to produce the desired calendering conditions for controlling the porosity of the resulting composite sheet. Calendering with only one heated roll increases opacity. By contrast, when both rolls are heated, the resulting sheet is translucent and more film- or paper-like, which is undesirable. Translucent, paper-like sheet often exhibits lower tensile strength but also especially lower tear strength This can be attributed to a significantly decreased contribution of individual fibers and significant loss of fiber orientation.
The preferred heated roll temperature according to the present invention is 140-155°C. The degree of porosity of the web depends, among others, on nip loading, which is the ratio of force applied to the sheet in the nip of the calender to the width of the sheet; the higher the nip loading the lower the porosity. Preferably, the nip loading should be about 1.75-3.50x10"5 N/m.
When forming a two-layer composite, the melt-blown polypropylene fiber web directly contacts the heated metal roll. This permits operation at a temperature lower than the melting point of polypropylene, although any temperature up to about 170°C can be used in principle.
When forming a three-layer composite, it is critical to the success of this process to use a low DTPF spunbonded sheet on the side in direct contact with the heated metal roll. This permits good heat transfer to and through the melt-blown web and results in good bonding of all three layers. The spunbonded sheet in contact with the unheated resilient roll usually will also be a low DTPF material.
In either case, whether making a two-layer composite or a three-layer composite, the adhesion of the spunbonded sheet not in contact with the heated metal roll can be further improved be preheating the sheet before the calendering step, for example, by contacting it with another metal roll heated to a temperature of about 20°C below the operating temperature of the metal calender roll.
Fig. 1 schematically illustrates the process of the present invention for making a two-layer composite, wherein 10 is the spunbonded sheet component, and 20 is the melt-blown web component; 1 is the heated metal roll, and 2 is the unheated resilient roll. The arrows show the direction of movement of the components and of the composite as well as the direction of rotation of the rolls. Fig. 2 schematically illustrates the process of the present invention for making a three-layer composite, wherein 30 and 40 are the spunbonded sheet components, and 50 is the melt-blown web component; 3 is the heated metal roll, and 4 is the unheated resilient roll. The arrows show the direction of movement of the components and of the composite as well as the direction of rotation of the rolls.
For use as a housewrap, the composite should have under standard temperature and pressure conditions a Gurley-Hill porosity of 30-75 seconds. Its water vapor transmission rate desirably should be at least 500 g/m2 in 24 hours or more. Liquid water permeability should be low. This property is normally evaluated by measuring the hydrostatic head pressure under standard conditions. Preferably, the hydrostatic head pressure should be at least 0.9 m. The tensile strength should be at least 3000 N per meter of width.
For use in sterile packaging, the Gurley-Hill porosity of the composite sheet should be 5-50 seconds. The composite sheet desirably should under standardized test conditions (to be described below) provide an effective barrier such that at least 60% of the test samples show no bacteria present. The tensile strength should be at least 1000 N per meter of width. Materials with a Gurley-Hill porosity of about 5-75 seconds have sometimes been used in the past for microfiltration of liquids. See, for example Lim et al, TYVEKfor Microfiltration Media, Fluid/Particle Separation Journal, Vol. 2, No. 1, March, 1989. Microfiltration elements can also be made from the composite sheets of the present invention.
This invention is now illustrated by the following examples of certain representative embodiments thereof. All units of weight and measure not originally obtained in SI units have been converted to SI units. Some of those figures have been rounded off.
TESTING
Those tests carried out according to ASTM standards are identified by their ASTM number. Other tests are identified according to their literature references given below, with any additional explanations given as appropriate.
Tensile strength - ASTM D 1682-64
Elongation - ASTM D 1682-64.
Elmendorf tear strength ASTM D 1423-83
Frazier porosity -ASTM D737-75 Water vapor transmission rate - ASTM E96, method B
Gurley-Hill porosity - TAPPI1 T-460 om-86. This test measures the time required for 100 cm^ of air to pass through a sample under standard conditions.
Hydrostatic head - AATCC2 Test Method 127-1985. The specimen is mounted under the orifice of a conical well and subjected to a steadily increasing water pressure, until three points of leakage appear on its undersurface.
Opacity - TAPPI T-519 om-86. The test reports the percentage of printed matter that is obscured by a single sheet of the test material
Bacteria barrier property - A bacterial test chamber (BTC), designed to hold several samples, has been devised by the DuPont Compay. A cloud of bacteria spores generated by a nebulizer is delivered
"•Technical Association cf the Pulp and Paper Industry 2American Association of Textile Chemists and Colorists to a closed BTC containing the test samples. All samples are subjected to vacuum simultaneously. The bacteria spores either do or do not pass through the samples. Bacteria spores which pass through the samples are collected on membrane filters. All membrane filters are removed and incubated to determine their bacteria population. The results are reported as percent of the samples resisting bacteria penetration. This test is described in Proceedings of the Tenth Technical Symposium of INDA (Association of the Nonowoven Fabrics Industry), November 17-19, 1992, New York, New York, S. K. Rudys, "Spunbonded Olefin in Medical Packaging".
In all the experiments, fibers of the spunbonded sheets had a diameter of 20 μm, and the fibers of the melt-blown webs had an average diameter of 1-10 μm. Example 1 - Two-layer composite for housewrap application The spunbonded polypropylene sheet was DUPONT's
TYPAR®.
The melt-blown web used in this Example was made by extruding molten polypropylene through a spinneret and fibrillating the extruded fibers at the spinneret with high temperature and high velocity air streams to form microfibers. The melt-blown fibers were formed into a sheet on a moving belt equipped with a suction box. The melt-blowing technology is being licensed for commercial use by Exxon Chemical Co.
The spunbonded polypropylene sheet and the melt-blown web were laminated by calendering in the nip formed between a smooth metal roll and a polyamide roll, which had a Shore D hardness of 78. The metal roll was heated to a surface temperature of 154°C. The polyamide roll was not heated. A load of 2.75xl0"5 N/m was applied to the sheet/web assembly as it advanced through the calender nip at a speed of 20 m per minute. The melt-blown web contacted the steel heated roll while the spunbonded sheet contacted the polyamide roll. Under these conditions, excellent adhesion between the spunbonded sheet and the melt-blown web was obtained. The resulting composite sheet exhibited high air flow resistance and high water vapor transmission rate properties. In addition, high tensile and tear strengths also were demonstrated. The physical properties of both starting webs as well as of the laminated composite sheet are given below in Table 1.
Table 1
TYPAR® Melt-blown Composite
Sheet weight, g/m2 67.8 40.7 108.5
Frazier porosity
(m^/minxm2) 92.4 9.8 «0.15
Gurley-Hill porosity
(seconds) «1 «1 30
MD/CD*Tensile strength (N/mxlO"3) 3.68/2.80 0.42/0.38 4.03/2.98
MD/CD* Elong. (%) 35/42 17/33 35/44
MD/CD* Elmendorf tear strength (N) 11/13 0.5/0.5 14/12
Hydrostatic head (m) ca.O 0.58 0.86
Opacity (%) 31 76 84
Water vapor transm.
Figure imgf000011_0001
* MD = machine direction; CD = cross direction
By contrast, when a composite sheet was made with the same spunbonded sheet contacting the heated roll and the melt-blown web contacting the polyamide roll, the lamination required a much higher operating temperature of 188°C. Further, adhesion of the melt-blown layer to the spunbonded layer was not as good, and the composite sheet exhibited low air flow resistance, as shown in Table 2.
Table 2
Heated roll Speed, Nip loading, Gurley-Hill Web in temp.,°C m/min N/mχl0"5 porosity, sec. contact with heated roll
188 20 3.00 1.5 Spunbonded 155 20 3.00 42.6 Melt-blown
Example 2 - Two-layer composite, variable calendering conditions
This example illustrates the range of air permeabilities that can be obtained by varying the nip loading and speed, at a constant temperature of 155°C. The spunbonded sheet was TYPAR® having a basis weight of 68 g/m2, while the melt-blown polypropylene web had a basis weight of 38 g/m2. The experimental conditions and results are presented in Table 3, below.
Table 3
Speed, m/min Nip pressure, N/mxl0~5 Gurley-Hill porosity, sec.
20 3.00 42.6 20 2.25 33.3 40 3.00 41.0 40 2.25 34.7 60 3.00 16.7 60 2.25 10.6 80 3.00 14.7 80 2.25 7.8
As can be seen, a wide range of permeabilities can be obtained by varying the calendering conditions. The permeability decreases, as evidenced by increasing Gurley-Hill porosity, with decreasing calendering speed and increasing nip loading. This suggests that longer residence time and higher consolidation force at the calender nip result in a better heat transfer through the melt-blown web, giving it characteristics similar to those of a membrane. Example 3 - Three-layer composite sheet for sterile packaging applications.
In this example, the composite had a core of melt-blown polypropylene fiber web and outer layers of spunbonded polypropylene sheets, where the spunbonded sheets were not TYPAR® but were made with filaments having a DTPF value of less than 6. The composite sheet formed a good barrier to bacteria and could be sterilized with steam.
The spunbonded web was made by extruding molten polypropylene through multiple spinneret orifices. The resulting filaments were quenched with controlled temperature air and suction fed through a venturi jet to a distribution chamber to ensure the fanning and entangling of the filaments. The entangled filaments were deposited as a random web on a moving belt, which had a suction box under it.
The melt-blown web used in this Example was prepared as in Example 1.
The two spunbonded outer layers and the melt-blown inner layer were laminated in the nip of a calender between a smooth metal roll and a cotton-filled roll having a Shore D hardness of 80-83. The metal roll was heated to a surface temperature of 149°C, while the cotton-filled roll was unheated. A load of 1.75x10"^ N/m was applied to the sheet as the sheet advanced through the calender nip at a speed of 59.4 m/min. The physical properties of the individual components as well as of the composite sheet are given in Table 4. It can be seen that air permeability of the composite was significantly lower, with higher hydrostatic head, than that of either the melt-blown web or the spunbonded sheet. A superior bacteria barrier property, with high hydrostatic head, also was achieved. By comparison, medical packaging paper with a basis weight of 67.8 g/m2, which is used extensively in sterile medical packaging, exhibits under the same test conditions a zero bacteria barrier property. Table 4
Spunbonded Melt-blown Composite
Basis wt (g/m2) 17 40.7 81.4
Frazier porosity
(m^/minxm2) >219 9.08 «0.15
Gurley-Hill porosity (s) «0.5 «0.5 41.5
MD/CD* Tensile str.
(N/mxlO-3) 0.38/0.28 0.40/0.28 1.70/0.56
MD/CD* Elongation
(%) 43.5/59.7 22.3/37.6 11.1/4.5
MD/CD* Elmendorf tear strength (N) 2.5/2.7 0.5/0.5 4.4/4.9
Hydrostatic head (m) 0.09 0.43 1.24
Opacity (%) 30.4 84 81
BTC test (%) 0 0 66.7
* MD = machine direction; CD = cross direction
Example 4 - Additional composites for sterile packaging
This example illustrates the range of permeability and bacteria barrier properties that can be achieved by use of the process of the present invention. In one series of runs, the nip loading was varied, while the calendering temperature was held constant at 143°C, and calendering speed was held constant at 59.4 m/min. In another series of runs, the calendering temperature was varied, while the nip loading was held constant at 1.75xl0~5 N/m, and the calendering speed was held constant at 59.4 m/min. The physical properties of the composite sheets from these two series of runs are shown, respectively, in Tables 5 and 6, below.
Table 5
Nip Loading (N/mχl0"5) Gurley-Hill porosity (sec) Hydrostatic head (m) =_= = = 19.9 === 1.16
2.26 43.0 1.36
3.50 70.1 1.38 Table 6
Temperature Gurley-Hill Hydrostatic Composite Medical
(°C) porosity head (m) BTC (%) paper* BTC (sec.) (%)
143 19.9 1.16 41.7 0
149 41.5 1.24 66.7 0
154 13.1 1.03 41.7 0
* Paper used for sterile packaging ("Monadnock") 67.8 g/m2
The above data show that, at constant temperature,
Gurley-Hill porosity and hydrostatic head increase with nip loading, indicating that the structure of the composite sheet becomes tighter. At constant nip loading and calendering speed, both Gurley-Hill porosity and hydrostatic head exhibited a maximum at 149°C. The BTC barrier property also reached a maximum at that temperature. Example 5 - Three-layer composite, with c zctrostaticάlly charged melt- blown web
This example illustrates a further improvement in the bacteria barrier property when an electrostatically charged melt-blown web is used as the inner layer of a three-layer composite of this invention. The melt-blown fibers are electrostatically charged in the web-forming step, e.g., as described in U.S. Patents 4,215,682 to Kubik et. al. (3M Company) and 4,904,174 to Mossmeyer (Exxon Company and Battelle Institute). The composite was made substantially as described in Example 3. The results are shown in Table 7, below.
Table 7
Electrostatic Gurley-Hill Hydrostatic BTC (%) charging porosity (sec). Head (m)
No 41.5 1.24 66.7
Yes 47.2 1.10 83.0 It is noted that, while the porosities and hydrostatic heads were not much affected by electrostatic charging of the melt-blown web, the bacteria barrier property was changed dramatically.

Claims

WE CLAIM:
1. A high-strength, tear-resistant, calendered, composite sheet having an opacity, as determined by TAPPI test T-519 om-86, of at least 75%, having low air permeability expressed as Gurley-Hill porosity of 5-75 seconds, high water vapor transmission rate of at least 500 g/m2 in 24 hours according to ASTM standard E96, method B, low liquid water permeability expressed by a hydrostatic head pressure of at least 0.75 m according to AATCC standard 127-1985, and barrier properties against bacteria that are significantly better than those of medical paper used for sterile packaging, which sheet comprises one melt-blown polypropylene fiber web and a spunbonded polypropylene fiber sheet laminated to at least one side thereof, the melt-blown fibers having an average diameter of 1-10 μm, the melt-blown fiber web itself having an average weight of about 17-40.7 g/m2, and the fibers of the spunbonded sheet having an average diameter of at least 20 μm, the spunbonded sheet itself having an average weight of about 17-100 g/m2.
2. A composite sheet of Claim 1 for use as a housewrap, which has a Gurley-Hill porosity 30-75 seconds.
3. A composite sheet of Claim 2 which has a water vapor transmission rate according to ASTM E96, method B of at least 500 g/m2 in 24 hours and a liquid water permeability expressed as hydrostatic head pressure of at least 0.9 m.
4. A composite sheet of Claim 1 for use in sterile packaging, which has a Gurley-Hill porosity of 5-50 seconds, which under standardized bacterial test chamber conditions provides an effective barrier to bacteria such that at least 60% of test samples show no bacteria present.
5. A composite sheet of Claim 1 wherein the melt-blown web is electrostatically charged.
6. A composite sheet of Claim 4 wherein the melt-blown web is electrostatically charged.
7. A two-layer composite sheet of Claim 1 wherein the fibers of the spunbonded sheet have a dtex per filament value of at least 10.
8. A three-layer composite sheet of Claim 1 wherein at least one of the spunbonded layers is made of fibers of less than 6 dtex per filament.
9. A microfiltration element made of a composite sheet of Claim 1.
10. A process for forming a composite sheet by calendering an assembly consisting of a melt-blown polypropylene fiber web and a spunbonded polypropylene fiber sheet laminated to at least one side thereof, the melt-blown fibers having an average diameter of 1-10 μm, the melt-blown fiber web itself having an average weight of about 17-40.7 g/m2, and the fibers of the spunbonded sheet having an average diameter of at least 20 μm, the spunbonded sheet itself having an average weight of about 17-100 g/m2, in a calender comprising a smooth metal roll heated to a temperature of 140-170°C, operating against an unheated, resilient roll having a Shore D hardness of 75-85, at a nip loading of about 1.75x10"5-3.5x10-5 N/m; with the proviso that when forming a two-layer composite sheet, only the melt-blown fiber web is in direct contact with the heated metal roll; and when forming a three-layer composite sheet, the spunbonded sheet in contact with the heated metal roll is made of filaments having a dtex-per- filament (DTPF) value of less than 6.
11. A process of Claim 7 wherein a two-layer composite sheet is made, and the melt-blown fibers of the web in contact with the heated metal roll have a dtex per fiber value of at least about 10.
12. A process of Claim 7 wherein the temperature of the heated metal roll is 140-150°C.
13. A process of Claim 7 wherein the layer in contact with the heated metal roll is preheated, prior to such contact, to a temperature of about 20°C below the temperature of the heated metal roll.
PCT/US1994/010592 1993-10-04 1994-09-30 Controlled-porosity, calendered spunbonded/melt blown laminates WO1995009728A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP51082595A JP3615549B2 (en) 1993-10-04 1994-09-30 Calendered spin bonded / melt blow molded laminate with controlled porosity
KR1019960701735A KR100323177B1 (en) 1993-10-04 1994-09-30 Calendared spunbonded / melt blown laminate
DE69402561T DE69402561T2 (en) 1993-10-04 1994-09-30 COMPOSITE LINES WITH CONTROLLED POROSITY FROM CALANDRATED MELT-BLOWED FLEECE AND FABRIC FABRIC
CA002173327A CA2173327C (en) 1993-10-04 1994-09-30 Controlled-porosity, calendered spunbonded/melt blown laminates
EP94929843A EP0722389B1 (en) 1993-10-04 1994-09-30 Controlled-porosity, calendered spunbonded/melt blown laminates

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/130,773 1993-10-04
US08/130,773 US5308691A (en) 1993-10-04 1993-10-04 Controlled-porosity, calendered spunbonded/melt blown laminates

Publications (1)

Publication Number Publication Date
WO1995009728A1 true WO1995009728A1 (en) 1995-04-13

Family

ID=22446262

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1994/010592 WO1995009728A1 (en) 1993-10-04 1994-09-30 Controlled-porosity, calendered spunbonded/melt blown laminates

Country Status (8)

Country Link
US (1) US5308691A (en)
EP (1) EP0722389B1 (en)
JP (1) JP3615549B2 (en)
KR (1) KR100323177B1 (en)
CA (1) CA2173327C (en)
DE (1) DE69402561T2 (en)
ES (1) ES2101579T3 (en)
WO (1) WO1995009728A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002068745A1 (en) * 2001-02-27 2002-09-06 E. I. Du Pont De Nemours And Company Tougher, softer nonwoven sheet product
EP1325185A1 (en) * 2000-10-06 2003-07-09 Polymer Group, Inc. Fine denier spunbond process and products thereof
WO2005059219A1 (en) * 2003-12-15 2005-06-30 E.I. Dupont De Nemours And Company Full-surface bonded multiple component melt-spun nonwoven web
EP1782945A1 (en) * 2005-06-07 2007-05-09 Cryovac, Inc. Breathable plastic packaging for produced products

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5690949A (en) * 1991-10-18 1997-11-25 Minnesota Mining And Manufacturing Company Microporous membrane material for preventing transmission of viral pathogens
US5935370A (en) * 1991-10-18 1999-08-10 #M Innovative Properties Company Minnesota Mining And Manufacturing Co. Method for laminating a viral barrier microporous membrane to a nonwoven web to prevent transmission of viral pathogens
CA2124237C (en) 1994-02-18 2004-11-02 Bernard Cohen Improved nonwoven barrier and method of making the same
CA2136576C (en) 1994-06-27 2005-03-08 Bernard Cohen Improved nonwoven barrier and method of making the same
US5455110A (en) * 1994-06-29 1995-10-03 Kimberly-Clark Corporation Nonwoven laminated fabrics
US5736473A (en) 1994-09-14 1998-04-07 Kimberly-Clark Corp. Fibrous composite structure including particulates
AU4961696A (en) 1994-12-08 1996-06-26 Kimberly-Clark Worldwide, Inc. Method of forming a particle size gradient in an absorbent article
CA2153278A1 (en) 1994-12-30 1996-07-01 Bernard Cohen Nonwoven laminate barrier material
US5540976A (en) * 1995-01-11 1996-07-30 Kimberly-Clark Corporation Nonwoven laminate with cross directional stretch
US5786058A (en) * 1995-04-03 1998-07-28 Minnesota Mining & Mfg Thermally bonded viral barrier composite
US5597647A (en) * 1995-04-20 1997-01-28 Kimberly-Clark Corporation Nonwoven protective laminate
GB9510234D0 (en) * 1995-05-20 1995-07-19 Advanced Allergy Technologies Allergen particle exclusion and/or retention covering
ZA965786B (en) 1995-07-19 1997-01-27 Kimberly Clark Co Nonwoven barrier and method of making the same
US5863639A (en) * 1995-09-13 1999-01-26 E. I. Du Pont De Nemours And Company Nonwoven sheet products made from plexifilamentary film fibril webs
US5834384A (en) 1995-11-28 1998-11-10 Kimberly-Clark Worldwide, Inc. Nonwoven webs with one or more surface treatments
US5763336A (en) * 1996-01-24 1998-06-09 E. I. Du Pont De Nemours And Company Bulky composite sheet material
EP0895551B1 (en) * 1996-04-23 2001-09-26 E.I. Du Pont De Nemours And Company Bonded polyolefin sheet
US20040097158A1 (en) * 1996-06-07 2004-05-20 Rudisill Edgar N. Nonwoven fibrous sheet structures
US5885909A (en) * 1996-06-07 1999-03-23 E. I. Du Pont De Nemours And Company Low or sub-denier nonwoven fibrous structures
US5851936A (en) * 1996-08-19 1998-12-22 E. I. Du Pont De Nemours And Company Elongation for flash spun products
US6034008A (en) * 1996-08-19 2000-03-07 E. I. Du Pont De Nemours And Company Flash-spun sheet material
DE69632956T2 (en) 1996-12-02 2005-07-28 Advanced Technology Materials, Inc., Danbury Lockable sterilizable bag
US5976220A (en) * 1996-12-09 1999-11-02 3M Innovative Properties Company Diffusional gas transfer system and method using same
AU8173898A (en) * 1997-06-30 1999-01-19 Kimberly-Clark Worldwide, Inc. Medical packaging paper
US6537932B1 (en) 1997-10-31 2003-03-25 Kimberly-Clark Worldwide, Inc. Sterilization wrap, applications therefor, and method of sterilizing
US6355333B1 (en) * 1997-12-09 2002-03-12 E. I. Du Pont De Nemours And Company Construction membrane
US6610163B1 (en) 1997-12-17 2003-08-26 Kimberly-Clark Worldwide, Inc. Enhanced barrier film and laminate and method for producing same
US6277479B1 (en) 1997-12-19 2001-08-21 Kimberly-Clark Worldwide, Inc. Microporous films having zoned breathability
US6365088B1 (en) 1998-06-26 2002-04-02 Kimberly-Clark Worldwide, Inc. Electret treatment of high loft and low density nonwoven webs
US6723669B1 (en) 1999-12-17 2004-04-20 Kimberly-Clark Worldwide, Inc. Fine multicomponent fiber webs and laminates thereof
EP1033238A1 (en) 1999-03-04 2000-09-06 Newform N.V. Seal for a sterilizable bag and method of making the same
US6413344B2 (en) * 1999-06-16 2002-07-02 First Quality Nonwovens, Inc. Method of making media of controlled porosity
JP2002030581A (en) * 2000-07-19 2002-01-31 Kuraray Co Ltd Laminated sheet for house wrap or roof ground cover
US20020132547A1 (en) * 2001-01-12 2002-09-19 Grondin Pierre D. Breathable nonwoven/film laminate
US20020148547A1 (en) * 2001-01-17 2002-10-17 Jean-Claude Abed Bonded layered nonwoven and method of producing same
US20030199217A1 (en) * 2002-04-15 2003-10-23 Reemay, Inc. Housewrap with drainage channels
CN1871402B (en) * 2003-10-22 2010-12-08 纳幕尔杜邦公司 Porous fibrous sheets of nanofibers
US8333918B2 (en) * 2003-10-27 2012-12-18 Kimberly-Clark Worldwide, Inc. Method for the production of nonwoven web materials
US20050139505A1 (en) * 2003-12-15 2005-06-30 Miller Mark R. Child-resistant blister package
US7487624B2 (en) * 2004-01-09 2009-02-10 E.I. Du Pont De Nemours And Company Breathable waterproof laminate structure
WO2005098118A1 (en) * 2004-04-09 2005-10-20 Mitsui Chemicals, Inc. Nonwoven fabric sheet and method for producing same
US7255759B2 (en) 2004-12-17 2007-08-14 Albany International Corp. Patterning on SMS product
DE602006004754D1 (en) * 2005-07-29 2009-02-26 Fiberweb Inc LIQUID, NON-FLUID LUBRICANT FROM BICOMPONENT FILAMENTS
US20070284280A1 (en) * 2006-06-12 2007-12-13 Patrick Henry Young Child-resistant blister package
US20080067099A1 (en) * 2006-09-14 2008-03-20 Patrick Henry Young Child resistant blister package
CN101516738B (en) * 2006-09-25 2012-10-17 高级技术材料公司 High integrity composite bags adapted for steam sterilization
US20090075033A1 (en) * 2007-09-14 2009-03-19 Theresa Ann Weston Building wrap for use in external wall assemblies having wet-applied facades
US20080236082A1 (en) * 2007-03-27 2008-10-02 Leahy Charles H Protective barrier material having low visual impact
US20090178355A1 (en) * 2008-01-12 2009-07-16 Bill Pugh Vapor-permeable, water-resistant sheathing and methods thereof
US20100154338A1 (en) * 2008-12-18 2010-06-24 Joseph Riccelli Composite house wrap
US8590264B2 (en) * 2009-06-29 2013-11-26 Charles H. Leahy Structural building panels with multi-laminate interlocking seams
US8539732B2 (en) * 2009-06-29 2013-09-24 Charles H. Leahy Structural building panels with seamless corners
US20110009024A1 (en) * 2009-07-01 2011-01-13 Berry Plastics Corporation Roof underlayment
US20110039468A1 (en) * 2009-08-12 2011-02-17 Baldwin Jr Alfred Frank Protective apparel having breathable film layer
GB2543434A (en) * 2011-10-13 2017-04-19 Don & Low Ltd Improved fabric
US20150247281A1 (en) 2014-02-28 2015-09-03 Avent, Inc. Reduced medical wet packs, post steam sterilization
GB2525103B (en) * 2014-08-22 2016-06-08 Don & Low Ltd Improved fabric
US10322562B2 (en) 2017-07-27 2019-06-18 Hollingsworth & Vose Company Medical protective clothing materials
TWI795248B (en) 2017-11-13 2023-03-01 美商比瑞全球股份有限公司 Nonwoven fabrics including multi-component fibers with improved inter-component adhesion and methods of forming the same
GB201720899D0 (en) * 2017-12-14 2018-01-31 Don & Low Ltd Improved nonwoven fabric
US11090901B2 (en) 2019-01-31 2021-08-17 Dupont Safety & Construction, Inc. Multilayer sheet structure
CN110359181A (en) * 2019-06-13 2019-10-22 大连华阳新材料科技股份有限公司 A method of for improving spun-bonded non-woven product of production line uniformity
CA3084635A1 (en) 2019-06-24 2020-12-24 Owens Corning Intellectual Capital, Llc Roofing underlayment with hydrophobic nonwoven core
CA3084636A1 (en) 2019-06-24 2020-12-24 Owens Corning Intellectual Capital, Llc Roofing underlayment with enhanced walkability and traction
KR102571795B1 (en) * 2020-04-09 2023-08-29 도레이첨단소재 주식회사 Non-woven fabric composite with reduced skin irritation, and article including the same
DE102021103701A1 (en) * 2021-02-17 2022-08-18 Carl Freudenberg Kg Use of a composite material as a packaging material, in particular for sterile packaging applications

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5391400A (en) * 1977-01-21 1978-08-11 Hitachi Ltd Composite insulated material and its manufacturing method
US4374888A (en) * 1981-09-25 1983-02-22 Kimberly-Clark Corporation Nonwoven laminate for recreation fabric
US4766029A (en) * 1987-01-23 1988-08-23 Kimberly-Clark Corporation Semi-permeable nonwoven laminate
US4828556A (en) * 1986-10-31 1989-05-09 Kimberly-Clark Corporation Breathable, multilayered, clothlike barrier
EP0370835A2 (en) * 1988-11-18 1990-05-30 Kimberly-Clark Corporation Nonwoven continuously-bonded trilaminate
EP0391725A1 (en) * 1989-04-07 1990-10-10 JOHNSON & JOHNSON MEDICAL, INC. Method for making an electrostatically charged face mask
JPH03167362A (en) * 1989-11-24 1991-07-19 Kuraray Co Ltd Agricultural sheet and bag-shaped material

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3978185A (en) * 1968-12-23 1976-08-31 Exxon Research And Engineering Company Melt blowing process
US4684568A (en) * 1986-04-21 1987-08-04 E. I. Du Pont De Nemours And Company Vapor-permeable liquid-impermeable fabric
US4898761A (en) * 1987-09-11 1990-02-06 Reemay, Inc. Barrier fabric and method
US4900619A (en) * 1988-10-17 1990-02-13 James River Corporation Translucent housewrap

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5391400A (en) * 1977-01-21 1978-08-11 Hitachi Ltd Composite insulated material and its manufacturing method
US4374888A (en) * 1981-09-25 1983-02-22 Kimberly-Clark Corporation Nonwoven laminate for recreation fabric
US4828556A (en) * 1986-10-31 1989-05-09 Kimberly-Clark Corporation Breathable, multilayered, clothlike barrier
US4766029A (en) * 1987-01-23 1988-08-23 Kimberly-Clark Corporation Semi-permeable nonwoven laminate
EP0370835A2 (en) * 1988-11-18 1990-05-30 Kimberly-Clark Corporation Nonwoven continuously-bonded trilaminate
EP0391725A1 (en) * 1989-04-07 1990-10-10 JOHNSON & JOHNSON MEDICAL, INC. Method for making an electrostatically charged face mask
JPH03167362A (en) * 1989-11-24 1991-07-19 Kuraray Co Ltd Agricultural sheet and bag-shaped material

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 7837, Derwent World Patents Index; AN 78-66246A *
PATENT ABSTRACTS OF JAPAN vol. 15, no. 409 (C - 0876) 18 October 1991 (1991-10-18) *
See also references of EP0722389A1 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1325185A1 (en) * 2000-10-06 2003-07-09 Polymer Group, Inc. Fine denier spunbond process and products thereof
EP1325185A4 (en) * 2000-10-06 2004-09-29 Polymer Group Inc Fine denier spunbond process and products thereof
WO2002068745A1 (en) * 2001-02-27 2002-09-06 E. I. Du Pont De Nemours And Company Tougher, softer nonwoven sheet product
WO2005059219A1 (en) * 2003-12-15 2005-06-30 E.I. Dupont De Nemours And Company Full-surface bonded multiple component melt-spun nonwoven web
US7452832B2 (en) 2003-12-15 2008-11-18 E.I. Du Pont De Nemors And Company Full-surface bonded multiple component melt-spun nonwoven web
EP1782945A1 (en) * 2005-06-07 2007-05-09 Cryovac, Inc. Breathable plastic packaging for produced products

Also Published As

Publication number Publication date
KR960704700A (en) 1996-10-09
CA2173327A1 (en) 1995-04-13
EP0722389B1 (en) 1997-04-09
US5308691A (en) 1994-05-03
EP0722389A1 (en) 1996-07-24
DE69402561T2 (en) 1997-09-25
KR100323177B1 (en) 2002-07-27
CA2173327C (en) 1999-08-10
JPH09503459A (en) 1997-04-08
JP3615549B2 (en) 2005-02-02
ES2101579T3 (en) 1997-07-01
DE69402561D1 (en) 1997-05-15

Similar Documents

Publication Publication Date Title
US5308691A (en) Controlled-porosity, calendered spunbonded/melt blown laminates
US5589258A (en) Non-woven fabric comprising at least one spunbonded layer
US5503907A (en) Barrier fabrics which incorporate multicomponent fiber support webs
EP0782504B1 (en) Microporous film/nonwoven composites
US4622259A (en) Nonwoven medical fabric
DE60124065T2 (en) RAILED COMPOSITE MATERIAL
US4657804A (en) Fusible fiber/microfine fiber laminate
KR101460838B1 (en) Breathable garment having a fluid drainage layer
GB2160475A (en) A soft nonwoven laminate
EP1846238A2 (en) Breathable composite sheet
JPH02133643A (en) Non-woven composite material
JPH0320507B2 (en)
US20030129910A1 (en) Multiple-layered nonwoven constructs for improved barrier performance
US20100292664A1 (en) Garment having a fluid drainage layer
KR20000031559A (en) Process for producing complicated nonwoven material which has improved phototransmittancy and bacteria interception
MXPA97002073A (en) Composite materials of microporosa / no tej film
MXPA97005278A (en) Method for providing a non-woven fabric with an amp union window

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): CA JP KR

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 1994929843

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2173327

Country of ref document: CA

WWP Wipo information: published in national office

Ref document number: 1994929843

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 1994929843

Country of ref document: EP