US20110152808A1 - Resilient absorbent coform nonwoven web - Google Patents

Resilient absorbent coform nonwoven web Download PDF

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Publication number
US20110152808A1
US20110152808A1 US12/643,051 US64305109A US2011152808A1 US 20110152808 A1 US20110152808 A1 US 20110152808A1 US 64305109 A US64305109 A US 64305109A US 2011152808 A1 US2011152808 A1 US 2011152808A1
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US
United States
Prior art keywords
web
mole
nonwoven web
fibers
coform nonwoven
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
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US12/643,051
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English (en)
Inventor
David M. Jackson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kimberly Clark Worldwide Inc
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Kimberly Clark Worldwide Inc
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44152106&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20110152808(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kimberly Clark Worldwide Inc filed Critical Kimberly Clark Worldwide Inc
Priority to US12/643,051 priority Critical patent/US20110152808A1/en
Assigned to KIMBERLY-CLARK WORLDWIDE, INC. reassignment KIMBERLY-CLARK WORLDWIDE, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JACKSON, DAVID M.
Priority to KR1020127015944A priority patent/KR101777433B1/ko
Priority to EP10838789.5A priority patent/EP2516710B1/de
Priority to AU2010334491A priority patent/AU2010334491B2/en
Priority to CN201080058729.4A priority patent/CN102791914B/zh
Priority to PCT/IB2010/055250 priority patent/WO2011077277A2/en
Priority to BR112012014276-3A priority patent/BR112012014276B1/pt
Priority to MX2012007197A priority patent/MX2012007197A/es
Priority to RU2012131064/12A priority patent/RU2527724C2/ru
Publication of US20110152808A1 publication Critical patent/US20110152808A1/en
Assigned to KIMBERLY-CLARK WORLDWIDE, INC. reassignment KIMBERLY-CLARK WORLDWIDE, INC. NAME CHANGE Assignors: KIMBERLY-CLARK WORLDWIDE, INC.
Priority to US15/134,608 priority patent/US10363338B2/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/24—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/724—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged forming webs during fibre formation, e.g. flash-spinning
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-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
    • D04H1/407—Non-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 containing absorbing substances, e.g. activated carbon
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577—Apparatus or processes for manufacturing
    • A61F13/15617—Making absorbent pads from fibres or pulverulent material with or without treatment of the fibres
    • A61F13/15658—Forming continuous, e.g. composite, fibrous webs, e.g. involving the application of pulverulent material on parts thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/53—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium
    • A61F13/538—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium characterised by specific fibre orientation or weave
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties
    • A61L15/60—Liquid-swellable gel-forming materials, e.g. super-absorbents
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/08—Melt spinning methods
    • D01D5/098—Melt spinning methods with simultaneous stretching
    • D01D5/0985—Melt spinning methods with simultaneous stretching by means of a flowing gas (e.g. melt-blowing)
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/04—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
    • D01F11/06—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/30—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising olefins as the major constituent
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-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
    • D04H1/42—Non-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 characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-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
    • D04H1/42—Non-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 characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282—Addition polymers
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-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
    • D04H1/42—Non-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 characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282—Addition polymers
    • D04H1/4291—Olefin series
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-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
    • D04H1/54—Non-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
    • D04H1/56—Non-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
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/005—Synthetic yarns or filaments
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING 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
    • D04H5/00—Non woven fabrics formed of mixtures of relatively short fibres and yarns or like filamentary material of substantial length
    • D04H5/08—Non woven fabrics formed of mixtures of relatively short fibres and yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of fibres or yarns
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/68—Melt-blown nonwoven fabric

Definitions

  • Coform nonwoven webs which are composites of a matrix of meltblown fibers and an absorbent material (e.g., pulp fibers), have been used as an absorbent layer in a wide variety of applications, including absorbent articles, absorbent dry wipes, wet wipes, and mops.
  • Most conventional coform webs employ meltblown fibers formed from polypropylene homopolymers.
  • coform materials may not be sufficiently resilient when subjected to bending forces. For example, when a coform wiper is crumpled, perhaps to wring a fluid from the wiper, the coform material may not return to its original flat, unwrinkled state.
  • a coform material used as an absorbent core in personal care absorbent product may have a tendency for bunching.
  • a resilient coform nonwoven web that includes a matrix of meltblown fibers and an absorbent material.
  • the meltblown fibers constitute from 45 wt % to about 99 wt % of the web and the absorbent material constitutes from about 1 wt % to about 55 wt % of the web.
  • the meltblown fibers are formed from a thermoplastic composition that contains at least one propylene/ ⁇ -olefin copolymer having a propylene content of from about 60 mole % to about 99.5 mole % and an ⁇ -olefin content of from about 0.5 mole % to about 40 mole %.
  • the copolymer further has a density of from about 0.86 to about 0.90 grams per cubic centimeter and the thermoplastic composition has melt flow rate of from about 200 to about 6000 grams per 10 minutes, determined at 230° C. in accordance with ASTM Test Method D1238-E.
  • the ⁇ -olefin includes ethylene.
  • the propylene constitutes from about 85 mole % to about 98 mole % of the copolymer and the ⁇ -olefin constitutes from about 2 mole % to about 15 mole % of the copolymer.
  • the copolymer has a density of from about 0.861 to about 0.89 grams per cubic centimeter, and preferably from about 0.862 to about 0.88 grams per cubic centimeter.
  • the propylene copolymer is single-site catalyzed.
  • the propylene/ ⁇ -olefin copolymer constitutes from about 15 wt % to about 99.9 wt % of the thermoplastic composition.
  • the melt flow rate of the thermoplastic composition is from about 170 to about 1500 grams per 10 minutes.
  • the thermoplastic composition includes from about 0.001 wt % to about 15 wt % of a surfactant.
  • the absorbent material includes pulp fibers. In a further embodiment, the absorbent material comprises superabsorbent polymer particles or superabsorbent polymer fibers.
  • the meltblown fibers constitute from 50 wt % to about 90 wt % of the web and the absorbent material constitutes from about 10 wt % to about 50 wt % of the web.
  • the web defines an exterior surface having a three-dimensional texture that includes a plurality of peaks and valleys.
  • an absorbent personal care article includes the resilient coform nonwoven web described above.
  • an absorbent personal care article includes a body-side liner, an absorbent core including the resilient coform nonwoven web described above, and a garment-side baffle.
  • a method of forming a resilient coform nonwoven web includes merging together a stream of an absorbent material with a stream of meltblown fibers to form a composite stream.
  • the meltblown fibers constitute from 45 wt % to about 99 wt % of the web and the absorbent material constitutes from about 1 wt % to about 55 wt % of the web.
  • the meltblown fibers are formed from a thermoplastic composition that contains at least one propylene/ ⁇ -olefin copolymer having a propylene content of from about 60 mole % to about 99.5 mole % and an ⁇ -olefin content of from about 0.5 mole % to about 40 mole %, wherein the copolymer further has a density of from about 0.86 to about 0.90 grams per cubic centimeter and the composition has a melt flow rate of from about 120 to about 6000 grams per 10 minutes, determined at 230° C. in accordance with ASTM Test Method D1238-E. Thereafter, the composite stream is collected on a forming surface to form a resilient coform nonwoven web.
  • the melt flow rate of the thermoplastic composition is from about 170 to about 1500 grams per 10 minutes.
  • the thermoplastic composition comprises from about 0.001 wt % to about 15 wt % of a surfactant.
  • the stream of absorbent material is merged together with first and second streams of meltblown fibers.
  • the first stream and second stream of meltblown fibers are supplied from respective first and second die heads, each of which is oriented at an angle of from about 45° to 55° relative to a plane tangent to the die heads.
  • the web is collected on a textured surface to define an exterior web surface having a three-dimensional texture that includes a plurality of peaks and valleys.
  • FIG. 1 is a schematic illustration one embodiment of a method for forming the coform web of the present invention
  • FIG. 2 is an illustration of certain features of the apparatus shown in FIG. 1 ;
  • FIG. 3 is a cross-sectional view of one embodiment of a textured coform nonwoven web formed according to the present invention.
  • FIG. 4 is a photo of one embodiment of a textured coform nonwoven web.
  • FIG. 5 is a photo of the textured coform nonwoven webs from FIG. 4 after being crumpled and allowed to relax.
  • FIG. 6 is a photo of another embodiment of a textured coform nonwoven web.
  • FIG. 7 is a photo of the textured coform nonwoven webs from FIG. 6 after being crumpled and allowed to relax.
  • FIG. 8 is a schematic side elevation of a feminine hygiene article.
  • nonwoven web generally refers to a web having a structure of individual fibers or threads which are interlaid, but not in an identifiable manner as in a knitted fabric.
  • nonwoven fabrics or webs include, but are not limited to, meltblown webs, spunbond webs, bonded carded webs, airlaid webs, coform webs, hydraulically entangled webs, and so forth.
  • meltblown web generally refers to a nonwoven web that is formed by a process in which a molten thermoplastic material is extruded through a plurality of fine, usually circular, die capillaries as molten fibers into converging high velocity gas (e.g., air) streams that attenuate the fibers of molten thermoplastic material to reduce their diameter, which may be to microfiber diameter. Thereafter, the meltblown fibers are carried by the high velocity gas stream and are deposited on a collecting surface to form a web of randomly dispersed meltblown fibers.
  • high velocity gas e.g., air
  • meltblown fibers may be microfibers that are substantially continuous or discontinuous, generally smaller than 10 micrometers in diameter, and generally tacky when deposited onto a collecting surface.
  • spunbond web generally refers to a web containing small diameter substantially continuous fibers.
  • the fibers are formed by extruding a molten thermoplastic material from a plurality of fine, usually circular, capillaries of a spinnerette with the diameter of the extruded fibers then being rapidly reduced as by, for example, eductive drawing and/or other well-known spunbonding mechanisms.
  • the production of spunbond webs is described and illustrated, for example, in U.S. Pat. Nos.
  • Spunbond fibers are generally not tacky when they are deposited onto a collecting surface. Spunbond fibers may sometimes have diameters less than about 40 micrometers, and are often between about 5 to about 20 micrometers.
  • the present invention is directed to a coform nonwoven web that contains a matrix of meltblown fibers and an absorbent material.
  • the meltblown fibers constitute from 45 wt % to about 99 wt % of the web and the absorbent material constitutes from about 1 wt % to about 55 wt % of the web.
  • the meltblown fibers are formed from a thermoplastic composition that contains at least one propylene/ ⁇ -olefin copolymer of a certain monomer content, density, melt flow rate, etc. The selection of a specific type of propylene/ ⁇ -olefin copolymer provides the resulting composition with improved thermal properties for forming a coform web.
  • the thermoplastic composition crystallizes at a relatively slow rate, thereby allowing the fibers to remain slightly tacky during formation.
  • This tackiness may provide a variety of benefits, such as enhancing the ability of the meltblown fibers to adhere to the absorbent material during web formation.
  • the meltblown fibers may constitute from about 45 wt % to about 99 wt %, in particular embodiments from about 50 wt % to about 90 wt %, and in more particular embodiments, from about 50 wt % to about 80 wt % of the coform web.
  • the absorbent material may constitute from about 1 wt % to about 55 wt %, in particular embodiments from 10 wt % to about 50 wt %, and in more particular embodiments, from about 20 wt % to about 50 wt % of the coform web.
  • the thermoplastic composition of the present invention may also impart other benefits to the resulting coform structure.
  • the coform web may be imparted with texture using a three-dimensional forming surface.
  • the relatively slow rate of crystallization of the meltblown fibers may increase their ability to conform to the contours of the three-dimensional forming surface.
  • the meltblown fibers may achieve a degree of resiliency greater than that of conventional polypropylene, thereby allowing them to both retain and regain the three-dimensional shape and highly textured surface on the coform web.
  • Another benefit of the fiber's prolonged tackiness during formation may be an increased ply attachment strength between layers of a multi-ply coform nonwoven web, resulting in additional shear energy being necessary to delaminate the plies.
  • Such increased ply attachment strength may reduce or eliminate the need for embossing that could negatively impact sheet characteristics such as thickness and density.
  • Increased ply attachment strength may be particularly desirable during dispensing of wipers made from a multi-ply coform nonwoven web. Texture imparted by using a three-dimensional forming surface as described herein may further increase the ply attachment strength by increasing the contact surface area between the plies.
  • thermoplastic composition of the present invention contains at least one copolymer of propylene and an ⁇ -olefin, such as a C 2 -C 20 ⁇ -olefin, C 2 -C 12 ⁇ -olefin, or C 2 -C 8 ⁇ -olefin.
  • Suitable ⁇ -olefins may be linear or branched (e.g., one or more C 1 -C 3 alkyl branches, or an aryl group).
  • Specific examples include ethylene, butene; 3-methyl-1-butene; 3,3-dimethyl-1-butene; pentene; pentene with one or more methyl, ethyl or propyl substituents; hexane with one or more methyl, ethyl or propyl substituents; heptene with one or more methyl, ethyl or propyl substituents; octene with one or more methyl, ethyl or propyl substituents; nonene with one or more methyl, ethyl or propyl substituents; ethyl, methyl or dimethyl-substituted decene; dodecene; styrene; and so forth.
  • Particularly desired ⁇ -olefin comonomers are ethylene, butene (e.g., 1-butene), 7exane, and octene (e.g., 1-octene or 2-octene).
  • the propylene content of such copolymers may be from about 60 mole % to about 99.5 mole %, in further embodiments from about 80 mole % to about 99 mole %, and in even further embodiments, from about 85 mole % to about 98 mole %.
  • the ⁇ -olefin content may likewise range from about 0.5 mole % to about 40 mole %, in further embodiments from about 1 mole % to about 20 mole %, and in even further embodiments, from about 2 mole % to about 15 mole %.
  • the distribution of the ⁇ -olefin comonomer is typically random and uniform among the differing molecular weight fractions forming the propylene copolymer.
  • the density of the propylene/ ⁇ -olefin copolymer may be a function of both the length and amount of the ⁇ -olefin. That is, the greater the length of the ⁇ -olefin and the greater the amount of ⁇ -olefin present, the lower the density of the copolymer. Generally speaking, copolymers with a higher density are better able to form a three-dimensional structure, while those with a lower density possess better elastomeric and resiliency properties.
  • the propylene/ ⁇ -olefin copolymer is normally selected to have a density of about 0.860 grams per cubic centimeter (g/cm 3 ) to about 0.900 g/cm 3 , in further embodiments from about 0.861 to about 0.890 g/cm 3 , and in even further embodiments, from about 0.862 g/cm 3 to about 0.880 g/cm 3 .
  • the density of the thermoplastic composition is normally selected to have a density of about 0.860 grams per cubic centimeter (g/cm 3 ) to about 0.940 g/cm 3 , in further embodiments from about 0.861 to about 0.920 g/cm 3 , and in even further embodiments, from about 0.862 g/cm 3 to about 0.900 g/cm 3 .
  • olefin polymers may be formed using a free radical or a coordination catalyst (e.g., Ziegler-Natta).
  • the copolymer is formed from a single-site coordination catalyst, such as a metallocene catalyst.
  • a coordination catalyst such as a metallocene catalyst.
  • metallocene catalyst Such a catalyst system produces propylene copolymers in which the co-monomer is randomly distributed within a molecular chain and uniformly distributed across the different molecular weight fractions.
  • Metallocene-catalyzed propylene copolymers are described, for instance, in U.S. Pat. Nos.
  • metallocene catalysts include bis(n-butylcyclopentadienyl)titanium dichloride, bis(n-butylcyclopentadienyl)zirconium dichloride, bis(cyclopentadienyl)scandium chloride, bis(indenyl)zirconium dichloride, bis(methylcyclopentadienyl)titanium dichloride, bis(methylcyclopentadienyl)zirconium dichloride, cobaltocene, cyclopentadienyltitanium trichloride, ferrocene, hafnocene dichloride, isopropyl(cyclopentadienyl,-1-flourenyl)zirconium dichloride, molybdocene dichloride, nickelocene, niobocene dichloride, ruthenocene, titanocene dichloride, zirconocene chloride hydr
  • metallocene catalysts typically have a narrow molecular weight range.
  • metallocene-catalyzed polymers may have polydispersity numbers (M w /M n ) of below 4, controlled short chain branching distribution, and controlled tacticity.
  • the propylene/ ⁇ -olefin copolymer constitutes about 50 wt % or more, in further embodiments about from 60 wt % or more, and in even further embodiments, about 75 wt % or more of the thermoplastic composition used to form the meltblown fibers.
  • the propylene/ ⁇ -olefin copolymer constitutes at least about 1 wt % and less than about 49 wt %, in particular embodiments from at least about 1% and less than about 45 wt %, in further embodiments from at least about 5% and less than about 45 wt %, and in even further embodiments, from at least about 5 wt % and less than about 35 wt % of the thermoplastic composition used to form the meltblown fibers.
  • other thermoplastic polymers may also be used to form the meltblown fibers so long as they do not adversely affect the desired properties of the composite.
  • the meltblown fibers may contain other polyolefins (e.g., polypropylene, polyethylene, etc.), polyesters, polyurethanes, polyamides, block copolymers, and so forth.
  • the meltblown fibers may contain an additional propylene polymer, such as homo polypropylene or a copolymer of propylene.
  • the additional propylene polymer may, for instance, be formed from a substantially isotactic polypropylene homopolymer or a copolymer containing equal to or less than about 10 weight percent of other monomer, i.e., at least about 90% by weight propylene.
  • Such a polypropylene may be present in the form of a graft, random, or block copolymer and may be predominantly crystalline in that it has a sharp melting point above about 110° C., in further embodiments about above 115° C., and in even further embodiments, above about 130° C.
  • additional polypropylenes are described in U.S. Pat. No. 6,992,159 to Datta, et al., which is incorporated herein in its entirety by reference thereto for all purposes.
  • additional polymer(s) may constitute from about 0.1 wt % to about 90 wt %, in further embodiments from about 0.5 wt % to about 50 wt %, and in even further embodiments, from about 1 wt % to about 30 wt % of the thermoplastic composition.
  • the above-described propylene/ ⁇ -olefin copolymer may constitute from about 15 wt % to about 99.9 wt %, in further embodiments from about 50 wt % to about 99.5 wt %, and in even further embodiments, from about 70 wt % to about 99 wt % of the thermoplastic composition.
  • the thermoplastic composition used to form the meltblown fibers may also contain other additives as is known in the art, such as surfactants, melt stabilizers, processing stabilizers, heat stabilizers, light stabilizers, antioxidants, heat aging stabilizers, whitening agents, etc.
  • Phosphite stabilizers e.g., IRGAFOS available from Ciba Specialty Chemicals of Tarrytown, N.Y. and DOVERPHOS available from Dover Chemical Corp. of Dover, Ohio
  • hindered amine stabilizers e.g., CHIMASSORB available from Ciba Specialty Chemicals
  • hindered phenols are commonly used as an antioxidant.
  • antioxidant, stabilizer, surfactants, etc. may each be present in an amount from about 0.001 wt % to about 15 wt %, in further embodiments, from about 0.005 wt % to about 10 wt %, and in even further embodiments, from about 0.01 wt % to about 5 wt % of the thermoplastic composition used to form the meltblown fibers.
  • One or more surfactants may be added to the polymer composition to make the polymer fibers more wettable and improve the fluid intake properties of the coform material.
  • Suitable surfactants include cationic, anionic, amphoteric, and nonionic surfactants.
  • a particularly suitable internal surfactant is available from Ciba is IRGASURF HL 560.
  • the surfactant may each be present in an amount from about 0.5 wt % to about 10 wt %, in further embodiments, from about 1.0 wt % to about 7.5 wt %, and in even further embodiments, from about 1.5 wt % to about 5 wt % of the thermoplastic composition used to form the meltblown fibers.
  • Surfactants may also be applied to the meltblown fibers externally as topical treatments.
  • the resulting thermoplastic composition may possess thermal properties superior to polypropylene homopolymers conventionally employed in meltblown webs.
  • the thermoplastic composition is generally more amorphous in nature than polypropylene homopolymers conventionally employed in meltblown webs.
  • the rate of crystallization of the thermoplastic composition is slower, as measured by its “crystallization half-time”—i.e., the time required for one-half of the material to become crystalline.
  • the thermoplastic composition typically has a crystallization half-time of greater than about 5 minutes, in further embodiments from about 5.25 minutes to about 20 minutes, and in even further embodiments, from about 5.5 minutes to about 12 minutes, determined at a temperature of 125° C.
  • the thermoplastic composition may have a melting temperature (“T m ”) of from about 100° C. to about 250° C., in further embodiments from about 110° C. to about 200° C., and in even further embodiments, from about 140° C. to about 180° C.
  • T m melting temperature
  • the thermoplastic composition may also have a crystallization temperature (“T c ”) (determined at a cooling rate of 10° C./min) of from about 50° C. to about 150° C., in further embodiments from about 80° C. to about 140° C., and in even further embodiments, from about 100° C. to about 120° C.
  • T c crystallization temperature
  • the crystallization half-time, melting temperature, and crystallization temperature may be determined using differential scanning calorimetry (“DSC”) as is well known to those skilled in the art.
  • the melt flow rate of the thermoplastic composition may also be selected within a certain range to optimize the properties of the resulting meltblown fibers.
  • the melt flow rate is the weight of a polymer (in grams) that may be forced through an extrusion rheometer orifice (0.0825-inch diameter) when subjected to a force of 2160 grams in 10 minutes at 230° C.
  • the melt flow rate is high enough to improve melt processability, but not so high as to adversely interfere with the binding properties of the fibers to the absorbent material.
  • the thermoplastic composition has a melt flow rate of from about 120 to about 6000 grams per 10 minutes, in further embodiments from about 150 to about 3000 grams per 10 minutes, and in even further embodiments, from about 170 to about 1500 grams per 10 minutes, measured in accordance with ASTM Test Method D1238-E.
  • the meltblown fibers may be monocomponent or multicomponent.
  • Monocomponent fibers are generally formed from a polymer or blend of polymers extruded from a single extruder.
  • Multicomponent fibers are generally formed from two or more polymers (e.g., bicomponent fibers) extruded from separate extruders.
  • the polymers may be arranged in substantially constantly positioned distinct zones across the cross-section of the fibers.
  • the components may be arranged in any desired configuration, such as sheath-core, side-by-side, pie, island-in-the-sea, three island, bull's eye, or various other arrangements known in the art.
  • Various methods for forming multicomponent fibers are described in U.S. Pat. Nos.
  • Multicomponent fibers having various irregular shapes may also be formed, such as described in U.S. Pat. Nos.
  • the absorbent material includes fibers formed by a variety of pulping processes, such as kraft pulp, sulfite pulp, thermomechanical pulp, etc.
  • the pulp fibers may include softwood fibers having an average fiber length of greater than 1 mm and particularly from about 2 to 5 mm based on a length-weighted average.
  • softwood fibers can include, but are not limited to, northern softwood, southern softwood, redwood, red cedar, hemlock, pine (e.g., southern pines), spruce (e.g., black spruce), combinations thereof, and so forth.
  • Exemplary commercially available pulp fibers suitable for the present invention include those available from Weyerhaeuser Co. of Federal Way, Wash. under the designation “Weyco CF-405.”
  • Hardwood fibers such as eucalyptus, maple, birch, aspen, and so forth, can also be used.
  • eucalyptus fibers may be particularly desired to increase the softness of the web.
  • Eucalyptus fibers can also enhance the brightness, increase the opacity, and change the pore structure of the web to increase its wicking ability.
  • secondary fibers obtained from recycled materials may be used, such as fiber pulp from sources such as, for example, newsprint, reclaimed paperboard, and office waste.
  • other natural fibers can also be used in the present invention, such as abaca, sabai grass, milkweed floss, pineapple leaf, and so forth.
  • synthetic fibers can also be utilized.
  • the absorbent material may also include a superabsorbent that is in the form fibers, particles, gels, etc.
  • superabsorbents are water-swellable materials capable of absorbing at least about 20 times its weight and, in some cases, at least about 30 times its weight in an aqueous solution containing 0.9 weight percent sodium chloride.
  • the superabsorbent may be formed from natural, synthetic and modified natural polymers and materials.
  • Examples of synthetic superabsorbent polymers include the alkali metal and ammonium salts of poly(acrylic acid) and poly(methacrylic acid), poly(acrylamides), poly(vinyl ethers), maleic anhydride copolymers with vinyl ethers and alpha-olefins, poly(vinyl pyrrolidone), poly(vinylmorpholinone), poly(vinyl alcohol), and mixtures and copolymers thereof.
  • superabsorbents include natural and modified natural polymers, such as hydrolyzed acrylonitrile-grafted starch, acrylic acid grafted starch, methyl cellulose, chitosan, carboxymethyl cellulose, hydroxypropyl cellulose, and the natural gums, such as alginates, xanthan gum, locust bean gum and so forth. Mixtures of natural and wholly or partially synthetic superabsorbent polymers may also be useful in the present invention. Particularly suitable superabsorbent polymers are HYSORB 8800AD (BASF of Charlotte, N.C. and FAVOR SXM 9300 (available from Evonik Stockhausen of Greensboro, N.C.).
  • the coform web of the present invention is generally made by a process in which at least one meltblown die head (e.g., two) is arranged near a chute through which the absorbent material is added while the web forms.
  • meltblown die head e.g., two
  • Some examples of such coform techniques are disclosed in U.S. Pat. Nos. 4,100,324 to Anderson, et al.; 5,350,624 to Georger, et al.; and 5,508,102 to Georger, et al., as well as U.S. Patent Application Publication Nos. 2003/0200991 to Keck, et al. and 2007/0049153 to Dunbar, et al., all of which are incorporated herein in their entirety by reference thereto for all purposes.
  • the apparatus includes a pellet hopper 12 or 12 ′ of an extruder 14 or 14 ′, respectively, into which a propylene/ ⁇ -olefin thermoplastic composition may be introduced.
  • the extruders 14 and 14 ′ each have an extrusion screw (not shown), which is driven by a conventional drive motor (not shown). As the polymer advances through the extruders 14 and 14 ′, it is progressively heated to a molten state due to rotation of the extrusion screw by the drive motor.
  • Heating may be accomplished in a plurality of discrete steps with its temperature being gradually elevated as it advances through discrete heating zones of the extruders 14 and 14 ′ toward two meltblowing dies 16 and 18 , respectively.
  • the meltblowing dies 16 and 18 may be yet another heating zone where the temperature of the thermoplastic resin is maintained at an elevated level for extrusion.
  • meltblowing die heads When two or more meltblowing die heads are used, such as described above, it should be understood that the fibers produced from the individual die heads may be different types of fibers. That is, one or more of the size, shape, or polymeric composition may differ, and furthermore the fibers may be monocomponent or multicomponent fibers.
  • larger fibers may be produced by the first meltblowing die head, such as those having an average diameter of about 10 micrometers or more, in further embodiments about 15 micrometers or more, and in even further embodiments, from about 20 to about 50 micrometers, while smaller fibers may be produced by the second die head, such as those having an average diameter of about 10 micrometers or less, in further embodiments about 7 micrometers or less, and in even further embodiments, from about 2 to about 6 micrometers.
  • each die head extrude approximately the same amount of polymer such that the relative percentage of the basis weight of the coform nonwoven web material resulting from each meltblowing die head is substantially the same.
  • meltblown fibrous nonwoven web material having a basis weight of 1.0 ounces per square yard or “osy” (34 grams per square meter or “gsm”)
  • first meltblowing die head may be desirable for the first meltblowing die head to produce about 30 percent of the basis weight of the meltblown fibrous nonwoven web material, while one or more subsequent meltblowing die heads produce the remainder 70 percent of the basis weight of the meltblown fibrous nonwoven web material.
  • the overall basis weight of the coform nonwoven web is from about 10 gsm to about 350 gsm, and more particularly from about 17 gsm to about 200 gsm, and still more particularly from about 25 gsm to about 150 gsm.
  • Each meltblowing die 16 and 18 is configured so that two streams of attenuating gas per die converge to form a single stream of gas which entrains and attenuates molten threads 20 as they exit small holes or orifices 24 in each meltblowing die.
  • the molten threads 20 are formed into fibers or, depending upon the degree of attenuation, microfibers, of a small diameter which is usually less than the diameter of the orifices 24 .
  • each meltblowing die 16 and 18 has a corresponding single stream of gas 26 and 28 containing entrained thermoplastic polymer fibers.
  • the gas streams 26 and 28 containing polymer fibers are aligned to converge at an impingement zone 30 .
  • the meltblowing die heads 16 and 18 are arranged at a certain angle with respect to the forming surface, such as described in U.S. Pat. Nos. 5,508,102 and 5,350,624 to Georger et al.
  • the meltblown dies 16 and 18 may be oriented at an angle ⁇ as measured from a plane “A” tangent to the two dies 16 and 18 .
  • the plane “A” is generally parallel to the forming surface 58 ( FIG. 1 ).
  • each die 16 and 18 is set at an angle ranging from about 30 to about 75 degrees, in further embodiments from about 35° to about 60°, and in even further embodiments from about 45° to about 55°.
  • the dies 16 and 18 may be oriented at the same or different angles. In fact, the texture of the coform web may actually be enhanced by orienting one die at an angle different than another die.
  • absorbent fibers 32 are added to the two streams 26 and 28 of thermoplastic polymer fibers 20 and 21 , respectively, and at the impingement zone 30 .
  • Introduction of the absorbent fibers 32 into the two streams 26 and 28 of thermoplastic polymer fibers 20 and 21 , respectively, is designed to produce a graduated distribution of absorbent fibers 32 within the combined streams 26 and 28 of thermoplastic polymer fibers. This may be accomplished by merging a secondary gas stream 34 containing the absorbent fibers 32 between the two streams 26 and 28 of thermoplastic polymer fibers 20 and 21 so that all three gas streams converge in a controlled manner. Because they remain relatively tacky and semi-molten after formation, the meltblown fibers 20 and 21 may simultaneously adhere and entangle with the absorbent fibers 32 upon contact therewith to form a coherent nonwoven structure.
  • any conventional equipment may be employed, such as a picker roll 36 arrangement having a plurality of teeth 38 adapted to separate a mat or batt 40 of absorbent fibers into the individual absorbent fibers.
  • the sheets or mats 40 of fibers 32 are fed to the picker roll 36 by a roller arrangement 42 .
  • the teeth 38 of the picker roll 36 After the teeth 38 of the picker roll 36 have separated the mat of fibers into separate absorbent fibers 32 , the individual fibers are conveyed toward the stream of thermoplastic polymer fibers through a nozzle 44 .
  • a housing 46 encloses the picker roll 36 and provides a passageway or gap 48 between the housing 46 and the surface of the teeth 38 of the picker roll 36 .
  • a gas for example, air
  • the gas duct 50 may enter the passageway or gap 48 at the junction 52 of the nozzle 44 and the gap 48 .
  • the gas is supplied in sufficient quantity to serve as a medium for conveying the absorbent fibers 32 through the nozzle 44 .
  • the gas supplied from the duct 50 also serves as an aid in removing the absorbent fibers 32 from the teeth 38 of the picker roll 36 .
  • the gas may be supplied by any conventional arrangement such as, for example, an air blower (not shown). It is contemplated that additives and/or other materials may be added to or entrained in the gas stream to treat the absorbent fibers.
  • the individual absorbent fibers 32 are typically conveyed through the nozzle 44 at about the velocity at which the absorbent fibers 32 leave the teeth 38 of the picker roll 36 .
  • the absorbent fibers 32 upon leaving the teeth 38 of the picker roll 36 and entering the nozzle 44 , generally maintain their velocity in both magnitude and direction from the point where they left the teeth 38 of the picker roll 36 .
  • Such an arrangement which is discussed in more detail in U.S. Pat. No. 4,100,324 to Anderson, et al.
  • the velocity of the secondary gas stream 34 may be adjusted to achieve coform structures of different properties.
  • the velocity of the secondary gas stream is adjusted so that it is greater than the velocity of each stream 26 and 28 of thermoplastic polymer fibers 20 and 21 upon contact at the impingement zone 30 , the absorbent fibers 32 are incorporated in the coform nonwoven web in a gradient structure. That is, the absorbent fibers 32 have a higher concentration between the outer surfaces of the coform nonwoven web than at the outer surfaces.
  • the absorbent fibers 32 are incorporated in the coform nonwoven web in a substantially homogenous fashion. That is, the concentration of the absorbent fibers is substantially the same throughout the coform nonwoven web. This is because the low-speed stream of absorbent fibers is drawn into a high-speed stream of thermoplastic polymer fibers to enhance turbulent mixing which results in a consistent distribution of the absorbent fibers.
  • a collecting device is located in the path of the composite stream 56 .
  • the collecting device may be a forming surface 58 (e.g., belt, drum, wire, fabric, etc.) driven by rollers 60 and that is rotating as indicated by the arrow 62 in FIG. 1 .
  • the merged streams of thermoplastic polymer fibers and absorbent fibers are collected as a coherent matrix of fibers on the surface of the forming surface 58 to form the coform nonwoven web 54 .
  • a vacuum box (not shown) may be employed to assist in drawing the near molten meltblown fibers onto the forming surface 58 .
  • the resulting textured coform structure 54 is coherent and may be removed from the forming surface 58 as a self-supporting nonwoven material.
  • first and second meltblowing die heads may be employed that extend substantially across a forming surface in a direction that is substantially transverse to the direction of movement of the forming surface.
  • the die heads may likewise be arranged in a substantially vertical disposition, i.e., perpendicular to the forming surface, so that the thus-produced meltblown fibers are blown directly down onto the forming surface.
  • Such a configuration is well known in the art and described in more detail in, for instance, U.S. Patent Application Publication No. 2007/0049153 to Dunbar, et al.
  • one embodiment of the present invention employs a forming surface 58 that is foraminous in nature so that the fibers may be drawn through the openings of the surface and form dimensional cloth-like tufts projecting from the surfaces of the material that correspond to the openings in the forming surface 58 .
  • the foraminous surface may be provided by any material that provides sufficient openings for penetration by some of the fibers, such as a highly permeable forming wire. Wire weave geometry and processing conditions may be used to alter the texture or tufts of the material.
  • the wire may have an open area of from about 35% and about 65%, in further embodiments from about 40% to about 60%, and in even further embodiments, from about 45% to about 55%.
  • One exemplary high open area forming surface is the forming wire FORMTECHTM 6 manufactured by Albany International Co. of Albany, N.Y.
  • Such a wire has a “mesh count” of about six strands by six strands per square inch (about 2.4 by 2.4 strands per square centimeter), i.e., resulting in about 36 foramina or “holes” per square inch (about 5.6 per square centimeter), and therefore capable of forming about 36 tufts or peaks in the material per square inch (about 5.6 peaks per square centimeter).
  • the FORMTECHTM 6 wire also has a warp diameter of about 1 millimeter polyester, a shute diameter of about 1.07 millimeters polyester, a nominal air permeability of approximately 41.8 m 3 /min (1475 ft 3 /min), a nominal caliper of about 0.2 centimeters (0.08 inch) and an open area of approximately 51%.
  • forming wire FORMTECHTM10 which has a mesh count of about 10 strands by 10 strands per square inch (about 4 by 4 strands per square centimeter), i.e., resulting in about 100 foramina or “holes” per square inch (about 15.5 per square centimeter), and therefore capable of forming about 100 tufts or peaks per square inch (about 15.5 peaks per square centimeter) in the material.
  • Still another suitable forming wire is FORMTECHTM 8, which has an open area of 47% and is also available from Albany International.
  • other forming wires and surfaces e.g., drums, plates, mats, etc. may be employed.
  • mats may be used with a depressions engraved in the surface such that the coform fibers will fill the depressions to result in tufts that correspond with the depressions.
  • the depressions (tufts) may take on various shapes, including, but not limited to, circles, squares, rectangles, swirls, ribs, lines, clouds, and so forth.
  • surface variations may include, but are not limited to, alternate weave patterns, alternate strand dimensions, release coatings (e.g., silicones, fluorochemicals, etc.), static dissipation treatments, and the like. Still other suitable foraminous surfaces that may be employed are described in U.S. Patent Application Publication No. 2007/0049153 to Dunbar, et al.
  • the tufts formed by the meltblown fibers of the present invention are better able to retain the desired shape and surface contour. Namely, because the meltblown fibers crystallize at a relatively slow rate, they are soft upon deposition onto the forming surface, which allows them to drape over and conform to the contours of the surface. After the fibers crystallize, they are then able to hold the shape and form tufts. The size and shape of the resulting tufts depends upon the type of forming surface used, the types of fibers deposited thereon, the volume of below wire air vacuum used to draw the fibers onto and into the forming surface, and other related factors.
  • the tufts may project from the surface of the material in the range of about 0.25 millimeters to at least about 9 millimeters, and in further embodiments, from about 0.5 millimeters to about 3 millimeters.
  • the tufts are filled with fibers and thus have desirable resiliency useful for wiping and scrubbing.
  • FIG. 3 shows an illustration of a cross section of a textured coform web 100 having a first exterior surface 122 and a second exterior surface 128 . At least one of the exterior surfaces has a three-dimensional surface texture.
  • the first exterior surface 122 has a three-dimensional surface texture that includes tufts or peaks 124 extending upwardly from the plane of the coform material.
  • the coform web typically has a peak to valley ratio of about 5 or less, in further embodiments from about 0.1 to about 4, and in even further embodiments, from about 0.5 to about 3.
  • the number and arrangement of the tufts 24 may vary widely depending on the desired end use. In particular embodiments that are more densely textured, the textured coform web will have from about 2 and about 70 tufts per square centimeter, and in other embodiments, from about 5 and 50 tufts per square centimeter.
  • the textured coform web will have from about 100 to about 20,000 tufts per square meter, and in further embodiments will have from about 200 to about 10,000 tufts per square meter.
  • the textured coform web may also exhibit a three-dimensional texture on the second surface of the web. This will especially be the case for lower basis weight materials, such as those having a basis weight of less than about 70 grams per square meter due to “mirroring”, wherein the second surface of the material exhibits peaks offset or between peaks on the first exterior surface of the material. In this case, the valley depth D is measured for both exterior surfaces as above and are then added together to determine an overall material valley depth.
  • the resilient coform nonwoven web may be used in a wide variety of articles.
  • the web may be incorporated into an “absorbent article” that is capable of absorbing water or other fluids.
  • absorbent articles include, but are not limited to, personal care absorbent articles, such as diapers, training pants, absorbent underpants, incontinence articles, feminine hygiene products (e.g., sanitary napkins), swim wear, baby wipes, mitt wipe, and so forth; medical absorbent articles, such as garments, fenestration materials, underpads, bedpads, bandages, absorbent drapes, and medical wipes; food service wipers; clothing articles; pouches; and so forth. Materials and processes suitable for forming such articles are well known to those skilled in the art.
  • the resilient coform of the present invention may form a component of the absorbent core or any other absorbent component of the absorbent article as is well known in the art.
  • the resilient coform nonwoven web may be used as an absorbent member in a feminine hygiene article.
  • a feminine hygiene article includes a peel strip 1 which adhesively attaches by means of a garment attachment adhesive 2 to a garment-side barrier film or baffle layer 3 on one side. The other side of the baffle 3 attaches to an absorbent layer 5 with construction adhesive 4 .
  • the absorbent layer 5 attaches to a body side liner 6 .
  • the resilient coform nonwoven web is suitable used as the absorbent layer 5 . Desirably, use of the resilient coform nonwoven web will inhibit bunching of the product as it is worn, hence improving overall effectiveness and reducing leakage.
  • the resilient coform nonwoven web has a textured surface.
  • the textured surface is desirably positioned towards the body side liner 5 to promote faster fluid intake and higher absorbency of the absorbent core.
  • the coform web is used to form a wipe.
  • the wipe may be formed entirely from the coform web or it may contain other materials, such as films, nonwoven webs (e.g., spunbond webs, meltblown webs, carded web materials, other coform webs, airlaid webs, etc.), paper products, and so forth.
  • nonwoven webs e.g., spunbond webs, meltblown webs, carded web materials, other coform webs, airlaid webs, etc.
  • two layers of a textured coform web may be laminated together to form the wipe, such as described in U.S. Patent Application Publication No. 2007/0065643 to Kopacz, which is incorporated herein in its entirety by reference thereto for all purposes.
  • one or both of the layers may be formed from the coform web of the present invention.
  • the wipe is a “wet” or “premoistened” wipe in that it contains a liquid solution for cleaning, disinfecting, sanitizing, etc.
  • melt flow rate is the weight of a polymer (in grams) forced through an extrusion rheometer orifice (0.0825-inch diameter) when subjected to a load of 2160 grams in 10 minutes at 230° C. Unless otherwise indicated, the melt flow rate was measured in accordance with ASTM Test Method D1238-E.
  • the melting temperature and crystallization temperature were determined by differential scanning calorimetry (DSC) in accordance with ASTM D-3417.
  • the differential scanning calorimeter was a DSC Q100 Differential Scanning Calorimeter, which was outfitted with a liquid nitrogen cooling accessory and with a UNIVERSAL ANALYSIS 2000 (version 4.6.6) analysis software program, both of which are available from T.A. Instruments Inc. of New Castle, Del.
  • tweezers or other tools were used.
  • the samples were placed into an aluminum pan and weighed to an accuracy of 0.01 milligram on an analytical balance.
  • a lid was crimped over the material sample onto the pan.
  • the resin pellets were placed directly in the weighing pan, and the fibers were cut to accommodate placement on the weighing pan and covering by the lid.
  • the differential scanning calorimeter was calibrated using an indium metal standard and a baseline correction was performed, as described in the operating manual for the differential scanning calorimeter.
  • a material sample was placed into the test chamber of the differential scanning calorimeter for testing, and an empty pan is used as a reference. All testing was run with a 55-cubic centimeter per minute nitrogen (industrial grade) purge on the test chamber.
  • the heating and cooling program was a 2-cycle test that began with an equilibration of the chamber to ⁇ 25° C., followed by a first heating period at a heating rate of 10° C. per minute to a temperature of 200° C., followed by equilibration of the sample at 200° C.
  • meltblown fibers were formed from the following polymer compositions:
  • the polymer compositions each further contained 3.0 wt % of surfactant (IRGASURF HL 560, available from Ciba).
  • IRGASURF HL 560 available from Ciba
  • the pulp fibers were fully treated southern softwood pulp obtained from the Weyerhaeuser Co. of Federal Way, Wash. under the designation “CF-405.”
  • the polymer for each meltblown fiber stream was supplied to respective meltblown dies at a rate of 2.0 pounds of polymer per inch of die tip per hour through 0.020 inch diameter holes to achieve a meltblown fiber content of 50 wt %.
  • the distance from the impingement zone to the forming wire i.e., the forming height
  • the distance between the tips of the meltblown dies was approximately 6 inches.
  • the meltblown die positioned upstream from the pulp fiber stream was oriented at an angle of 48° relative to the pulp stream, while the other meltblown die (positioned downstream from the pulp stream) was oriented at an angle of 48° relative to the pulp stream.
  • the forming wire was FORMTECHTM 8 (Albany International Co.).
  • rubber mats were disposed on the upper surface of the forming wire.
  • One such mat had a thickness of approximately 0.95 centimeters and contained holes arranged in a hexagonal array. The holes had a diameter of approximately 0.64 centimeters and were spaced apart approximately 0.95 centimeters (center-to-center). Mats of other patterns (e.g., clouds) were also used.
  • a vacuum box was positioned below the forming wire to aid in deposition of the web and was set to 30 inches of water.
  • FIG. 4 shows a photo of Example 1 samples prior to crumpling.
  • FIG. 5 shows a photo of Example 1 samples after completion of the crumple test.
  • FIG. 6 shows a photo of Example 3 samples prior to crumpling.
  • Example 7 shows a photo of Example 3 samples after completion of the crumple test. As can be seen in FIGS. 4-7 the Example 3 samples were much more resilient, i.e., opened out much flatter after the crumple test, than Example 1. It was likewise found that the Example 2 samples behaved similar to the Example 3 samples.

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US12/643,051 US20110152808A1 (en) 2009-12-21 2009-12-21 Resilient absorbent coform nonwoven web
RU2012131064/12A RU2527724C2 (ru) 2009-12-21 2010-11-17 Эластичное впитывающее нетканое полотно, изготовленное совместным формованием
MX2012007197A MX2012007197A (es) 2009-12-21 2010-11-17 Tela no tejida coform absorbente elastica.
PCT/IB2010/055250 WO2011077277A2 (en) 2009-12-21 2010-11-17 Resilient absorbent coform nonwoven web
EP10838789.5A EP2516710B1 (de) 2009-12-21 2010-11-17 Elastisches und saugfähiges koform-vlies
AU2010334491A AU2010334491B2 (en) 2009-12-21 2010-11-17 Resilient absorbent coform nonwoven web
CN201080058729.4A CN102791914B (zh) 2009-12-21 2010-11-17 弹性吸收性同成形非织造纤网
KR1020127015944A KR101777433B1 (ko) 2009-12-21 2010-11-17 탄성 흡수 코폼 부직 웹
BR112012014276-3A BR112012014276B1 (pt) 2009-12-21 2010-11-17 trama não tecida de coform resiliente, artigo de cuidado pessoal absorvente, e, método de formação de uma trama não tecida de coform resiliente
US15/134,608 US10363338B2 (en) 2009-12-21 2016-04-21 Resilient absorbent coform nonwoven web

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140246159A1 (en) * 2011-09-29 2014-09-04 Unicharm Corporation Wet wipe and method for manufacturing the same
US20140316362A1 (en) * 2011-12-06 2014-10-23 Borealis Ag Pp copolymers for melt blown/pulp fibrous nonwoven structures with improved mechanical properties and lower hot air consumption
US9260808B2 (en) 2009-12-21 2016-02-16 Kimberly-Clark Worldwide, Inc. Flexible coform nonwoven web
US20170226675A1 (en) * 2013-12-11 2017-08-10 Kyung-Ju Choi System and process for making a polymeric fiberous material having increased beta content
US10363338B2 (en) 2009-12-21 2019-07-30 Kimberly-Clark Worldwide, Inc. Resilient absorbent coform nonwoven web
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US11192327B2 (en) * 2017-07-03 2021-12-07 Axel Nickel Voluminous meltblown nonwoven fabric with improved stackability and storability
US11464385B2 (en) 2017-03-27 2022-10-11 Sellars Absorbent Materials, Inc. Absorbent laminated material
US11725309B2 (en) 2015-06-03 2023-08-15 The Procter & Gamble Company Coforming processes and forming boxes used therein

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US20200306096A1 (en) * 2019-03-29 2020-10-01 The Procter & Gamble Company Nonwoven suitable for use in absorbent article
WO2021126188A1 (en) * 2019-12-18 2021-06-24 Kimberly-Clark Worldwide, Inc. Nonwoven web with increased cd strength
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CN112080858B (zh) * 2020-08-31 2022-06-24 临海市恒泰无纺布有限公司 一种熔喷布的生产方法、及接收辊筒
CN113350042B (zh) * 2021-04-22 2022-08-23 苏州谷原生物科技有限公司 一种超细纤维复合芯体的制备方法

Citations (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3034180A (en) * 1959-09-04 1962-05-15 Kimberly Clark Co Manufacture of cellulosic products
US3110609A (en) * 1959-04-30 1963-11-12 Kimberly Clark Co Cellulosic product
US4042740A (en) * 1974-09-20 1977-08-16 Minnesota Mining And Manufacturing Company Reinforced pillowed microfiber webs
US4100324A (en) * 1974-03-26 1978-07-11 Kimberly-Clark Corporation Nonwoven fabric and method of producing same
US4103058A (en) * 1974-09-20 1978-07-25 Minnesota Mining And Manufacturing Company Pillowed web of blown microfibers
US4637819A (en) * 1985-05-31 1987-01-20 The Procter & Gamble Company Macroscopically expanded three-dimensional polymeric web for transmitting both dynamically deposited and statically contacted fluids from one surface to the other
US4741941A (en) * 1985-11-04 1988-05-03 Kimberly-Clark Corporation Nonwoven web with projections
US4762521A (en) * 1986-04-11 1988-08-09 Kimberly-Clark Corporation Absorbent garment with quilted and conformable absorbent pad
US5149335A (en) * 1990-02-23 1992-09-22 Kimberly-Clark Corporation Absorbent structure
US5180620A (en) * 1989-07-18 1993-01-19 Mitsui Petrochemical Industries, Ltd. Nonwoven fabric comprising meltblown fibers having projections extending from the fabric base
US5213881A (en) * 1990-06-18 1993-05-25 Kimberly-Clark Corporation Nonwoven web with improved barrier properties
US5242632A (en) * 1989-07-18 1993-09-07 Mitsui Petrochemical Industries, Ltd. Nonwoven fabric and a method of manufacturing the same
US5350624A (en) * 1992-10-05 1994-09-27 Kimberly-Clark Corporation Abrasion resistant fibrous nonwoven composite structure
US5575874A (en) * 1993-04-29 1996-11-19 Kimberly-Clark Corporation Method for making shaped nonwoven fabric
US5665396A (en) * 1992-12-31 1997-09-09 Mcneil-Ppc, Inc. Apparatus for making three-dimensional fabrics
US5733274A (en) * 1988-03-31 1998-03-31 The Procter & Gamble Company Sanitary napkin having stiffened center
US6039839A (en) * 1998-02-03 2000-03-21 The Procter & Gamble Company Method for making paper structures having a decorative pattern
US6127595A (en) * 1998-04-22 2000-10-03 Air Products And Chemicals, Inc. Cover sheet lamination for absorbent article and low temperature lamination process
US6245051B1 (en) * 1999-02-03 2001-06-12 Kimberly-Clark Worldwide, Inc. Absorbent article with a liquid distribution, belt component
US20020155776A1 (en) * 1999-10-15 2002-10-24 Mitchler Patricia Ann Particle-containing meltblown webs
US20030113463A1 (en) * 2001-12-14 2003-06-19 Ko Young C. Process for adding superabsorbent to a pre-formed fibrous web via in situ polymerization
US20030120249A1 (en) * 2001-12-20 2003-06-26 Wulz Andrea Susan Absorbent article having an insert providing for improved fluid distribution
US20030120233A1 (en) * 2001-12-20 2003-06-26 The Procter & Gamble Company Disposable absorbent article having a raised circumferential bank
US20030149411A1 (en) * 1999-08-23 2003-08-07 Keuhn Charles Paul Absorbent article with increased wet breathability
US20030176136A1 (en) * 2002-01-10 2003-09-18 Wadsworth Larry C. Biodegradable cotton composites
US20030200991A1 (en) * 2002-04-29 2003-10-30 Kimberly-Clark Worldwide, Inc. Dual texture absorbent nonwoven web
US20040102751A1 (en) * 2002-11-27 2004-05-27 Kimberly-Clark Worldwide, Inc. Absorbent article with reinforced absorbent structure
US20040253892A1 (en) * 2003-06-13 2004-12-16 Kimberly-Clark Worldwide, Inc. Absorbent structure having three-dimensional topography on upper and lower surfaces
US20040265534A1 (en) * 2002-12-20 2004-12-30 The Procter & Gamble Company Tufted laminate web
US6896669B2 (en) * 2001-12-21 2005-05-24 Kimberly-Clark Worldwide, Inc. Composite absorbent members
US20050148261A1 (en) * 2003-12-30 2005-07-07 Kimberly-Clark Worldwide, Inc. Nonwoven webs having reduced lint and slough
US20050228350A1 (en) * 2004-04-08 2005-10-13 Sridhar Ranganathan Differentially expanding absorbent structure
US20060063456A1 (en) * 2004-09-22 2006-03-23 Pgi Polymer, Inc. Nonwoven wiping fabrics having variable surface topography
US20060141881A1 (en) * 2002-03-08 2006-06-29 3M Innovative Properties Company Wipe
US7101622B2 (en) * 2004-03-19 2006-09-05 Dow Global Technologies Inc. Propylene-based copolymers, a method of making the fibers and articles made from the fibers
US20060199006A1 (en) * 2004-03-17 2006-09-07 Dow Global Technologies Inc. Fibers made from copolymers of propylene/alpha-olefins
US20070049153A1 (en) * 2005-08-31 2007-03-01 Dunbar Charlene H Textured wiper material with multi-modal pore size distribution
US20070065643A1 (en) * 2001-10-09 2007-03-22 Kimberly-Clark Worldwide, Inc. Methods for producing internally-tufted laminates
US20080119103A1 (en) * 2006-11-22 2008-05-22 Wing-Chak Ng Strand composite having latent elasticity
US20080177242A1 (en) * 2005-03-17 2008-07-24 Dow Global Technologies Inc. Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates
US20090111347A1 (en) * 2006-05-25 2009-04-30 Hong Peng Soft and extensible polypropylene based spunbond nonwovens
US8043984B2 (en) * 2003-12-31 2011-10-25 Kimberly-Clark Worldwide, Inc. Single sided stretch bonded laminates, and methods of making same

Family Cites Families (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4531945A (en) 1983-10-31 1985-07-30 Kimberly-Clark Corporation Multi layer sanitary appliance
US4724114A (en) 1984-04-23 1988-02-09 Kimberly-Clark Corporation Selective layering of superabsorbents in meltblown substrates
US5096995A (en) 1987-08-13 1992-03-17 Toray Industries, Inc. Polyether-ester amide and permanently antistatic resin composition
US4931355A (en) 1988-03-18 1990-06-05 Radwanski Fred R Nonwoven fibrous hydraulically entangled non-elastic coform material and method of formation thereof
US4879170A (en) 1988-03-18 1989-11-07 Kimberly-Clark Corporation Nonwoven fibrous hydraulically entangled elastic coform material and method of formation thereof
US4965122A (en) * 1988-09-23 1990-10-23 Kimberly-Clark Corporation Reversibly necked material
US5482772A (en) 1992-12-28 1996-01-09 Kimberly-Clark Corporation Polymeric strands including a propylene polymer composition and nonwoven fabric and articles made therewith
US5652326A (en) 1993-03-03 1997-07-29 Sanyo Chemical Industries, Ltd. Polyetheresteramide and antistatic resin composition
JP3061507B2 (ja) 1993-03-24 2000-07-10 三井化学株式会社 体液吸収性物品の表面シート、その製造方法、およびその製造装置
WO1994028219A1 (en) 1993-05-25 1994-12-08 Exxon Chemical Patents Inc. Novel polyolefin fibers and their fabrics
US5423786A (en) 1993-09-24 1995-06-13 Mcneil-Ppc, Inc. Stabilized absorbent core and products made therefrom
CA2134594A1 (en) 1994-04-12 1995-10-13 Kimberly-Clark Worldwide, Inc. Method for making soft tissue products
ES2132758T5 (es) 1994-11-30 2003-08-16 Procter & Gamble Nucleo de articulos absorbentes estirables.
US5560878A (en) 1994-11-30 1996-10-01 The Procter & Gamble Company Method and apparatus for making stretchable absorbent articles
US5562645A (en) 1995-05-31 1996-10-08 Kimberly-Clark Corporation Article with soft absorbent pulp sheet
US5952251A (en) * 1995-06-30 1999-09-14 Kimberly-Clark Corporation Coformed dispersible nonwoven fabric bonded with a hybrid system
US5843055A (en) 1996-07-24 1998-12-01 The Procter & Gamble Company Stratified, multi-functional fluid absorbent members
US5879343A (en) * 1996-11-22 1999-03-09 Kimberly-Clark Worldwide, Inc. Highly efficient surge material for absorbent articles
US5964743A (en) 1997-02-27 1999-10-12 Kimberly-Clark Worldwide, Inc. Elastic absorbent material for personal care products
US5969026A (en) 1997-06-26 1999-10-19 Techmer Pm Wettable polymer fibers
JP4026926B2 (ja) 1998-04-06 2007-12-26 三井化学株式会社 紙おむつ用トップシートおよび紙おむつ用多層不織布
WO1999062370A1 (fr) 1998-05-29 1999-12-09 Kao Corporation Brosse jetable
DE19846857C1 (de) * 1998-10-12 2000-03-02 Freudenberg Carl Fa Perforierter Vliesstoff und Verfahren zu dessen Herstellung
US6231557B1 (en) 1999-09-01 2001-05-15 Kimberly-Clark Worldwide, Inc. Absorbent product containing an elastic absorbent component
US6362389B1 (en) 1998-11-20 2002-03-26 Kimberly-Clark Worldwide, Inc. Elastic absorbent structures
JP3467432B2 (ja) 1999-06-24 2003-11-17 ユニ・チャーム株式会社 使い捨て着用物品の可撓性シート
US6680423B1 (en) 1999-08-27 2004-01-20 Kimberly-Clark Worldwide, Inc. Absorbent article having reinforced elastic absorbent core
US6627789B1 (en) 1999-10-14 2003-09-30 Kimberly-Clark Worldwide, Inc. Personal care product with fluid partitioning
DE60110290T2 (de) 2000-02-28 2005-10-06 Kao Corp. Blatt für einen absorbierenden Artikel und absorbierender Artikel mit einem solchen Blatt
JP2002339221A (ja) 2001-03-13 2002-11-27 Toyoda Spinning & Weaving Co Ltd 立体不織布及びその製造方法
US7045029B2 (en) 2001-05-31 2006-05-16 Kimberly-Clark Worldwide, Inc. Structured material and method of producing the same
US20030135178A1 (en) 2002-01-17 2003-07-17 Hansen Ebba A. Absorbent laminate
US20030211802A1 (en) 2002-05-10 2003-11-13 Kimberly-Clark Worldwide, Inc. Three-dimensional coform nonwoven web
US20030236511A1 (en) 2002-06-25 2003-12-25 Jones Archie L. Compressed absorbent web
US20040005457A1 (en) 2002-07-03 2004-01-08 Kimberly-Clark Worldwide, Inc. Methods of improving the softness of fibers and nonwoven webs and fibers and nonwoven webs having improved softness
US20040054343A1 (en) 2002-09-18 2004-03-18 Barnett Larry N. Horizontal density gradient absorbent system for personal care products
MY139729A (en) * 2002-11-25 2009-10-30 Mitsui Chemicals Inc Nonwoven fabric capable of being elongated and composite nonwoven fabric comprising said nonwoven fabric laminated
AR042713A1 (es) 2003-01-13 2005-06-29 Kimberly Clark Co Un articulo absorbente para la higiene femenina
WO2004073479A2 (en) 2003-02-19 2004-09-02 The Procter & Gamble Company Cleaning sheets
US9018112B2 (en) * 2003-11-18 2015-04-28 Exxonmobil Chemicals Patents Inc. Extensible polypropylene-based nonwovens
JP4233435B2 (ja) 2003-11-20 2009-03-04 花王株式会社 複合シート
US7662745B2 (en) 2003-12-18 2010-02-16 Kimberly-Clark Corporation Stretchable absorbent composites having high permeability
WO2005065932A1 (en) 2003-12-31 2005-07-21 Kimberly-Clark Worldwide, Inc. Single sided stretch bonded laminates, and method of making same
US8198200B2 (en) * 2004-03-29 2012-06-12 The Procter & Gamble Company Web materials having both plastic and elastic properties
DE602005026514D1 (de) 2004-04-30 2011-04-07 Dow Global Technologies Inc Verbesserter vliesstoff und verbesserte fasern
JP4318597B2 (ja) 2004-06-18 2009-08-26 花王株式会社 立体不織布
US7772456B2 (en) 2004-06-30 2010-08-10 Kimberly-Clark Worldwide, Inc. Stretchable absorbent composite with low superaborbent shake-out
US20060184149A1 (en) 2004-08-20 2006-08-17 Kao Corporation Absorbent article
EP1634556B1 (de) 2004-09-13 2019-06-12 The Procter & Gamble Company Absorbierender Artikel mit erhöhter Aufnahmegeschwindigkeit
JP4455241B2 (ja) 2004-09-14 2010-04-21 ユニ・チャーム株式会社 生理用ナプキン
US7594904B2 (en) 2004-09-16 2009-09-29 Mcneil-Ppc, Inc. Drapeable sanitary absorbent napkin
EP1920099A1 (de) * 2005-08-19 2008-05-14 Dow Gloval Technologies Inc. Propylenbasierte schmelzblasvliesstoffe und verbundkörper
TW200718814A (en) * 2005-11-08 2007-05-16 Kao Corp Stretchable nonwoven fabric
US20070135785A1 (en) 2005-12-12 2007-06-14 Jian Qin Absorbent articles comprising thermoplastic coated superabsorbent polymer materials
EP1991729B2 (de) 2006-02-21 2015-09-16 Fitesa Nonwoven, Inc. Dehnbare absorbierende zusammensetzungen
CN101460123A (zh) * 2006-06-07 2009-06-17 宝洁公司 用于吸收制品的可双轴向拉伸的外覆盖件
JP5123511B2 (ja) 2006-06-23 2013-01-23 ユニ・チャーム株式会社 不織布
US7803244B2 (en) * 2006-08-31 2010-09-28 Kimberly-Clark Worldwide, Inc. Nonwoven composite containing an apertured elastic film
MX2009006136A (es) 2006-12-15 2009-08-07 Kimberly Clark Co Acidos polilacticos biodegradables para uso en la formacion de fibras.
DK2116367T3 (en) * 2007-03-02 2018-05-14 Mitsui Chemicals Inc LAYERED NON-WOVEN FABRICS
CN107080621A (zh) 2007-06-12 2017-08-22 德科技控股有限公司 具有狭缝吸收芯的吸收制品
US8481634B2 (en) 2007-09-07 2013-07-09 Bostik, Inc. Hot melt desiccant matrix composition based on plasticized polyolefin binder
US20090233049A1 (en) * 2008-03-11 2009-09-17 Kimberly-Clark Worldwide, Inc. Coform Nonwoven Web Formed from Propylene/Alpha-Olefin Meltblown Fibers
US20110152808A1 (en) 2009-12-21 2011-06-23 Jackson David M Resilient absorbent coform nonwoven web

Patent Citations (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3110609A (en) * 1959-04-30 1963-11-12 Kimberly Clark Co Cellulosic product
US3034180A (en) * 1959-09-04 1962-05-15 Kimberly Clark Co Manufacture of cellulosic products
US4100324A (en) * 1974-03-26 1978-07-11 Kimberly-Clark Corporation Nonwoven fabric and method of producing same
US4042740A (en) * 1974-09-20 1977-08-16 Minnesota Mining And Manufacturing Company Reinforced pillowed microfiber webs
US4103058A (en) * 1974-09-20 1978-07-25 Minnesota Mining And Manufacturing Company Pillowed web of blown microfibers
US4637819A (en) * 1985-05-31 1987-01-20 The Procter & Gamble Company Macroscopically expanded three-dimensional polymeric web for transmitting both dynamically deposited and statically contacted fluids from one surface to the other
US4741941A (en) * 1985-11-04 1988-05-03 Kimberly-Clark Corporation Nonwoven web with projections
US4762521A (en) * 1986-04-11 1988-08-09 Kimberly-Clark Corporation Absorbent garment with quilted and conformable absorbent pad
US5733274A (en) * 1988-03-31 1998-03-31 The Procter & Gamble Company Sanitary napkin having stiffened center
US5180620A (en) * 1989-07-18 1993-01-19 Mitsui Petrochemical Industries, Ltd. Nonwoven fabric comprising meltblown fibers having projections extending from the fabric base
US5242632A (en) * 1989-07-18 1993-09-07 Mitsui Petrochemical Industries, Ltd. Nonwoven fabric and a method of manufacturing the same
US5149335A (en) * 1990-02-23 1992-09-22 Kimberly-Clark Corporation Absorbent structure
US5213881A (en) * 1990-06-18 1993-05-25 Kimberly-Clark Corporation Nonwoven web with improved barrier properties
US5350624A (en) * 1992-10-05 1994-09-27 Kimberly-Clark Corporation Abrasion resistant fibrous nonwoven composite structure
US5508102A (en) * 1992-10-05 1996-04-16 Kimberly-Clark Corporation Abrasion resistant fibrous nonwoven composite structure
US5665396A (en) * 1992-12-31 1997-09-09 Mcneil-Ppc, Inc. Apparatus for making three-dimensional fabrics
US5575874A (en) * 1993-04-29 1996-11-19 Kimberly-Clark Corporation Method for making shaped nonwoven fabric
US5643653A (en) * 1993-04-29 1997-07-01 Kimberly-Clark Corporation Shaped nonwoven fabric
US6039839A (en) * 1998-02-03 2000-03-21 The Procter & Gamble Company Method for making paper structures having a decorative pattern
US6127595A (en) * 1998-04-22 2000-10-03 Air Products And Chemicals, Inc. Cover sheet lamination for absorbent article and low temperature lamination process
US6245051B1 (en) * 1999-02-03 2001-06-12 Kimberly-Clark Worldwide, Inc. Absorbent article with a liquid distribution, belt component
US20030149411A1 (en) * 1999-08-23 2003-08-07 Keuhn Charles Paul Absorbent article with increased wet breathability
US20020155776A1 (en) * 1999-10-15 2002-10-24 Mitchler Patricia Ann Particle-containing meltblown webs
US20070065643A1 (en) * 2001-10-09 2007-03-22 Kimberly-Clark Worldwide, Inc. Methods for producing internally-tufted laminates
US20030113463A1 (en) * 2001-12-14 2003-06-19 Ko Young C. Process for adding superabsorbent to a pre-formed fibrous web via in situ polymerization
US20030120233A1 (en) * 2001-12-20 2003-06-26 The Procter & Gamble Company Disposable absorbent article having a raised circumferential bank
US20030120249A1 (en) * 2001-12-20 2003-06-26 Wulz Andrea Susan Absorbent article having an insert providing for improved fluid distribution
US6896669B2 (en) * 2001-12-21 2005-05-24 Kimberly-Clark Worldwide, Inc. Composite absorbent members
US20030176136A1 (en) * 2002-01-10 2003-09-18 Wadsworth Larry C. Biodegradable cotton composites
US20060141881A1 (en) * 2002-03-08 2006-06-29 3M Innovative Properties Company Wipe
US20030200991A1 (en) * 2002-04-29 2003-10-30 Kimberly-Clark Worldwide, Inc. Dual texture absorbent nonwoven web
US20040102751A1 (en) * 2002-11-27 2004-05-27 Kimberly-Clark Worldwide, Inc. Absorbent article with reinforced absorbent structure
US20040265534A1 (en) * 2002-12-20 2004-12-30 The Procter & Gamble Company Tufted laminate web
US20040253892A1 (en) * 2003-06-13 2004-12-16 Kimberly-Clark Worldwide, Inc. Absorbent structure having three-dimensional topography on upper and lower surfaces
US20050148261A1 (en) * 2003-12-30 2005-07-07 Kimberly-Clark Worldwide, Inc. Nonwoven webs having reduced lint and slough
US8043984B2 (en) * 2003-12-31 2011-10-25 Kimberly-Clark Worldwide, Inc. Single sided stretch bonded laminates, and methods of making same
US20060199006A1 (en) * 2004-03-17 2006-09-07 Dow Global Technologies Inc. Fibers made from copolymers of propylene/alpha-olefins
US7101622B2 (en) * 2004-03-19 2006-09-05 Dow Global Technologies Inc. Propylene-based copolymers, a method of making the fibers and articles made from the fibers
US20050228350A1 (en) * 2004-04-08 2005-10-13 Sridhar Ranganathan Differentially expanding absorbent structure
US20060063456A1 (en) * 2004-09-22 2006-03-23 Pgi Polymer, Inc. Nonwoven wiping fabrics having variable surface topography
US20080177242A1 (en) * 2005-03-17 2008-07-24 Dow Global Technologies Inc. Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates
US20070049153A1 (en) * 2005-08-31 2007-03-01 Dunbar Charlene H Textured wiper material with multi-modal pore size distribution
US20090111347A1 (en) * 2006-05-25 2009-04-30 Hong Peng Soft and extensible polypropylene based spunbond nonwovens
US20080119103A1 (en) * 2006-11-22 2008-05-22 Wing-Chak Ng Strand composite having latent elasticity

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9260808B2 (en) 2009-12-21 2016-02-16 Kimberly-Clark Worldwide, Inc. Flexible coform nonwoven web
US10363338B2 (en) 2009-12-21 2019-07-30 Kimberly-Clark Worldwide, Inc. Resilient absorbent coform nonwoven web
US20140246159A1 (en) * 2011-09-29 2014-09-04 Unicharm Corporation Wet wipe and method for manufacturing the same
US9074323B2 (en) * 2011-09-29 2015-07-07 Unicharm Corporation Wet wipe and method for manufacturing the same
US20140316362A1 (en) * 2011-12-06 2014-10-23 Borealis Ag Pp copolymers for melt blown/pulp fibrous nonwoven structures with improved mechanical properties and lower hot air consumption
US20170226675A1 (en) * 2013-12-11 2017-08-10 Kyung-Ju Choi System and process for making a polymeric fiberous material having increased beta content
US10683878B2 (en) 2014-12-19 2020-06-16 The Procter & Gamble Company Spatially controllable eductor for managing solid additives and processes using same
US11313386B2 (en) 2014-12-19 2022-04-26 The Procter & Gamble Company Spatially controllable eductor for managing solid additives and processes using same
US11725309B2 (en) 2015-06-03 2023-08-15 The Procter & Gamble Company Coforming processes and forming boxes used therein
US10801141B2 (en) 2016-05-24 2020-10-13 The Procter & Gamble Company Fibrous nonwoven coform web structure with visible shaped particles, and method for manufacture
US11464385B2 (en) 2017-03-27 2022-10-11 Sellars Absorbent Materials, Inc. Absorbent laminated material
US11192327B2 (en) * 2017-07-03 2021-12-07 Axel Nickel Voluminous meltblown nonwoven fabric with improved stackability and storability

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CN102791914A (zh) 2012-11-21
EP2516710A2 (de) 2012-10-31
MX2012007197A (es) 2012-07-10
KR20120106768A (ko) 2012-09-26
EP2516710B1 (de) 2016-01-27
KR101777433B1 (ko) 2017-09-11
US20160228596A1 (en) 2016-08-11
RU2527724C2 (ru) 2014-09-10
BR112012014276B1 (pt) 2020-12-29
CN102791914B (zh) 2015-07-29
EP2516710A4 (de) 2013-05-22
WO2011077277A3 (en) 2011-11-24
RU2012131064A (ru) 2014-01-27
AU2010334491B2 (en) 2013-11-14
BR112012014276A2 (pt) 2017-03-01
WO2011077277A2 (en) 2011-06-30
US10363338B2 (en) 2019-07-30

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