AU748366B2 - Absorbent structures having fluid distribution and storage layers - Google Patents
Absorbent structures having fluid distribution and storage layers Download PDFInfo
- Publication number
- AU748366B2 AU748366B2 AU43391/99A AU4339199A AU748366B2 AU 748366 B2 AU748366 B2 AU 748366B2 AU 43391/99 A AU43391/99 A AU 43391/99A AU 4339199 A AU4339199 A AU 4339199A AU 748366 B2 AU748366 B2 AU 748366B2
- Authority
- AU
- Australia
- Prior art keywords
- layer
- fibers
- acquisition
- cellulose
- gsm
- 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.)
- Ceased
Links
- 239000002250 absorbent Substances 0.000 title claims description 83
- 230000002745 absorbent Effects 0.000 title claims description 83
- 238000009826 distribution Methods 0.000 title claims description 83
- 239000012530 fluid Substances 0.000 title claims description 82
- 238000003860 storage Methods 0.000 title claims description 66
- 239000000835 fiber Substances 0.000 claims description 151
- 229920002678 cellulose Polymers 0.000 claims description 63
- 239000001913 cellulose Substances 0.000 claims description 63
- 239000004816 latex Substances 0.000 claims description 52
- 229920000126 latex Polymers 0.000 claims description 52
- 239000011159 matrix material Substances 0.000 claims description 50
- 229920003043 Cellulose fiber Polymers 0.000 claims description 47
- 229920000247 superabsorbent polymer Polymers 0.000 claims description 40
- 239000007788 liquid Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 18
- 239000002245 particle Substances 0.000 claims description 18
- -1 polyethylene Polymers 0.000 claims description 17
- 238000004891 communication Methods 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 10
- 239000000839 emulsion Substances 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 7
- 229920000573 polyethylene Polymers 0.000 claims description 7
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 239000002174 Styrene-butadiene Substances 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 229920000058 polyacrylate Polymers 0.000 claims description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- 239000011115 styrene butadiene Substances 0.000 claims description 6
- 229920000742 Cotton Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 239000002023 wood Substances 0.000 claims description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 3
- 229920000578 graft copolymer Polymers 0.000 claims description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 229920002785 Croscarmellose sodium Polymers 0.000 claims description 2
- 229920002125 Sokalan® Polymers 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 229920006163 vinyl copolymer Polymers 0.000 claims description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims 1
- 239000010410 layer Substances 0.000 description 226
- 229920000728 polyester Polymers 0.000 description 50
- 239000011162 core material Substances 0.000 description 47
- 239000000463 material Substances 0.000 description 36
- 241000157282 Aesculus Species 0.000 description 28
- 235000010181 horse chestnut Nutrition 0.000 description 28
- 239000000047 product Substances 0.000 description 27
- 239000000523 sample Substances 0.000 description 25
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 21
- 239000011230 binding agent Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- 239000000843 powder Substances 0.000 description 17
- 229920002994 synthetic fiber Polymers 0.000 description 15
- 239000012209 synthetic fiber Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- 239000011780 sodium chloride Substances 0.000 description 14
- 229920004935 Trevira® Polymers 0.000 description 13
- 239000002131 composite material Substances 0.000 description 13
- 238000005516 engineering process Methods 0.000 description 13
- 206010021639 Incontinence Diseases 0.000 description 11
- 229920001169 thermoplastic Polymers 0.000 description 11
- 239000004416 thermosoftening plastic Substances 0.000 description 11
- 230000014759 maintenance of location Effects 0.000 description 10
- 239000011148 porous material Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- 230000000717 retained effect Effects 0.000 description 4
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 3
- 238000003490 calendering Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000017 hydrogel Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000013074 reference sample Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920013683 Celanese Polymers 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004583 superabsorbent polymers (SAPs) Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000012815 thermoplastic material Substances 0.000 description 2
- 238000012549 training Methods 0.000 description 2
- 229920001634 Copolyester Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920001410 Microfiber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- NPERTKSDHFSDLC-UHFFFAOYSA-N ethenol;prop-2-enoic acid Chemical compound OC=C.OC(=O)C=C NPERTKSDHFSDLC-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
Classifications
-
- 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
- A61F13/534—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 having an inhomogeneous composition through the thickness of the pad
- A61F13/537—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer
- A61F13/53708—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer the layer having a promotional function on liquid propagation in at least one direction
- A61F13/53713—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer the layer having a promotional function on liquid propagation in at least one direction the layer having a promotional function on liquid propagation in the vertical direction
-
- 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
- A61F13/534—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 having an inhomogeneous composition through the thickness of the pad
- A61F13/537—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer
- A61F13/53743—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer characterised by the position of the layer relative to the other layers
-
- 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
- A61F13/534—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 having an inhomogeneous composition through the thickness of the pad
- A61F13/537—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer
- A61F13/5376—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 having an inhomogeneous composition through the thickness of the pad characterised by a layer facilitating or inhibiting flow in one direction or plane, e.g. a wicking layer characterised by the performance of the layer, e.g. acquisition rate, distribution time, transfer time
-
- 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
- A61F13/15203—Properties of the article, e.g. stiffness or absorbency
- A61F2013/15284—Properties of the article, e.g. stiffness or absorbency characterized by quantifiable properties
- A61F2013/15406—Basis weight
-
- 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
- A61F13/15203—Properties of the article, e.g. stiffness or absorbency
- A61F2013/15284—Properties of the article, e.g. stiffness or absorbency characterized by quantifiable properties
- A61F2013/15447—Fibre dimension, e.g. denier or tex
-
- 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]
- Y10T442/659—Including an additional nonwoven fabric
-
- 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]
- Y10T442/659—Including an additional nonwoven fabric
- Y10T442/664—Including a wood fiber containing layer
-
- 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]
- Y10T442/659—Including an additional nonwoven fabric
- Y10T442/668—Separate nonwoven fabric layers comprise chemically different strand or fiber material
-
- 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]
- Y10T442/659—Including an additional nonwoven fabric
- Y10T442/673—Including particulate material other than fiber
-
- 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]
- Y10T442/697—Containing at least two chemically different strand or fiber materials
- Y10T442/698—Containing polymeric and natural strand or fiber materials
-
- 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]
- Y10T442/699—Including particulate material other than strand or fiber material
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Laminated Bodies (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
- Nonwoven Fabrics (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Description
P:\WIf)OCS\CAB\SPECI\7554630dO-27/0202 -1- ABSORBENT STRUCTURES HAVING FLUID DISTRIBUTION AND STORAGE LAYERS This application claims priority from U.S. Provisional Application Serial Nos.
60/088,455 and 60/088,456 filed June 8, 1998, U.S. Provisional Application Serial No.
60/102,344 filed September 29, 1998, and U.S. Patent Application Serial No. 09/232,783 filed January 19, 1999.
FIELD OF THE INVENTION The present invention is directed to improved fibrous absorbent structures having i: separate layers for fluid acquisition, distribution and storage. The acquisition layer contains latex-bonded synthetic fibers, and is useful in providing improved disposable absorbent products, such as diapers, adult incontinence pads, and sanitary napkins.
o• BACKGROUND OF THE INVENTION Absorbent articles such as disposable diapers, adult incontinence pads, sanitary napkins, and the like, are generally provided with an absorbent core, or storage layer, to receive and retain bodily liquids. The absorbent core is usually sandwiched between a liquid pervious top sheet, whose function is to allow the passage of fluid to the core, and a liquid impervious backsheet which contains the fluid and prevents it from passing through the absorbent article. An absorbent core for diapers and adult incontinence pads) typically includes fibrous batts or webs constructed of defiberized, loose, fluffed, hydrophilic, cellulosic fibers. The core may also include superabsorbent polymer (SAP) particles, granules, flakes or fibers. In addition, an absorbent article may contain a distribution layer that aids in transporting liquid quickly from the acquisition layer to the storage layer of the core.
In recent years, market demand for thinner and more comfortable absorbent articles Shas increased. Such articles may be obtained by decreasing the WO 99/63922 PCT/US99/13175 thickness of the diaper core, by reducing the amount of fibrous material used in the core while increasing the amount of SAP particles, and by calendering or compressing the core to reduce caliper and hence, increase density. However, higher density cores do not absorb liquid as rapidly as lower density cores because densification of the core results in smaller effective pore size. Accordingly, to maintain a suitable liquid absorption rate, it is necessary to provide a lower density layer having a larger pore size above the high density absorbent core to increase the rate of uptake of liquid discharged onto the absorbent article. The low density layer is typically referred to as an acquisition layer.
The storage layer portion of a disposable diaper core for example, is generally formed in place, during the converting process, from loose, fluffed cellulose. Superabsorbent powder is blended with the fluff cellulose fibers as the absorbent core is formed on the diaper converting line. Such cellulose material is generally not available in preformed roll form because it exhibits insufficient web strength, due to the lack of interfiber bonding or entanglement.
The acquisition layer portion of a disposable diaper is generally a carded synthetic staple fiber web that is thermally bonded, latex bonded, or point bonded. Typical staple fibers for acquisition layers are crimped polyester (PET) or polypropylene fibers that have a size of 6 to 15 denier and a length of at least mm. The acquisition layer is formed, bonded and slit as a homogenous rolled good on a dedicated nonwoven textile production line. The slit roll of acquisition layer material is subsequently unrolled onto the diaper converting line where it is affixed on top of the absorbent core and below the topsheet. Examples of commercial infant diapers with a bonded carded staple fiber are Huggies Diapers produced by Kimberly-Clark Corp. (Dallas, TX) and private label diapers produced by Paragon Trade Brands (Atlanta, GA).
Modern infant disposable diaper converting machines have become extremely complex as more and more features such as elastication and multiple nonwovens have been implemented to improve diaper performance. This complexity has created significant raw material handling issues and a resultant loss of converting line productivity. There is a need to replace the bulky and cumbersome fluff pulp and superabsorbent powder forming systems with a single WO 99/63922 PCT/US99/13175 material that can simply be fed directly into the converting line from a roll or other suitable compact package. Because the acquisition layer and absorbent core are placed together in the final product, it can maximize the efficiency of the converting operation to combine the fluid acquisition layer and the absorbent core in a single material.
Ultra-thin feminine napkins are generally produced from roll-goods based nonwoven material. Such a roll of preformed absorbent core material is unwound directly onto the absorbent article converting equipment without the defiberization step required for fluff-based products, such as diapers and incontinence pads. The nonwoven web is typically bonded or consolidated in a fashion that gives it sufficient strength to be handled in the converting process.
The web may also contain SAP particles.
The web consolidation mechanisms used in the roll-goods approach to making preformed cores provide strength and dimensional stability to the web.
Such mechanisms include latex bonding, bonding with thermoplastic or bicomponent fibers or thermoplastic powders, hydroentanglement, needlepunching, carding, or the like.
One embodiment of a structure having an acquisition layer and a distribution layer (an "ADL") typically found on die-cut feminine hygiene pads is an airlaid cellulose web bonded with an aqueous binder resin that has been dried and cured. Airlaid materials typically retain up to 16 g of fluid per gram of material against gravity under negligible load. Thus, an ADL can acquire a surge of fluid within the absorbent product until the superabsorbent particles in the absorbent core can absorb the retained fluid out of the airlaid cellulose ADL and into final storage containing superabsorbent particles.
An example of a conventional airlaid cellulose material is Vicell 6002 (Buckeye Technologies Inc., Memphis TN), which is a 105 gsm (grams per square meter) airlaid cellulose non-woven bonded with a vinyl acetate binder resin. Vicell 6002 is prepared by spraying an aqueous emulsion of the vinyl acetate binder resin onto the airlaid cellulose web followed by drying and curing in a hot air oven. It is used commercially in an ADL for feminine hygiene pads.
The disadvantage of certain commercially available airlaid cellulose WO 99/63922 PCT/US99/13175 structures is that they may collapse under normal use. This typically occurs when the structure is compressed by the weight of the wearer and particularly when the structure becomes wet. This structural collapse significantly reduces the fluid acquisition rate of the absorbent product and thus increases the chance of leakage.
When a completely or partially fluid saturated airlaid cellulose structure collapses, the fluid escapes from the ADL and the product feels wet against the wearer's skin.
There is a need for thin absorbent core material which facilitates fluid transport from an acquisition zone to a storage zone, has a high absorbent capacity in use, and can be delivered in roll-goods form to simplify the manufacturing and converting processes.
Applicants have now surprisingly discovered an improved ADL containing at least two discrete layers, the top and the bottom layer, which overcomes the above-described disadvantage of commercially available products.
The top layer the layer in contact with the skin of wearer) of the ADL of the present invention is highly porous, thus preventing the collapse of the structure and minimizing the leakage problem.
SUMMARY OF THE INVENTION The present invention provides a highly absorbent, high-bulk low density article having an absorbent structure comprising a liquid acquisition and, optionally, a distribution layer and a fibrous liquid storage layer in communication with the acquisition layer. The storage layer contains SAP particles, latex-bonded fibers, thermally bonded-fibers, or a combination thereof.
In one embodiment, the invention relates to an improved acquisition and distribution layer (ADL) having at least two layers for use in disposable absorbent products, a top (acquisition) layer in contact with the wearer of the absorbent product, and a bottom (distribution) layer between the top layer and a storage layer. Thus, according to one aspect of the invention, an improved ADL with a highly porous acquisition layer is provided.
In another aspect of the invention, an airlaid rolled good containing the ADL of the invention, and a method for its production is provided.
In yet another aspect of the invention, a disposable absorbent product P:\WP()OCS\CAB\SPEp75563.d27/O2/2 containing the ADL of the invention, and a method for its production is provided.
The present invention as claimed provides a fluid acquisition and distribution structure comprising: a porous top acquisition layer comprising latex-bonded, synthetic matrix fibers, said matrix fibers having a length of from about 3 to about 15 mm; and (ii) a bottom distribution layer in fluid communication with said top layer, comprising airlaid cellulose fibers, and a bonder selected from the group consisting of thermoplastic fibers, latex, and mixtures thereof.
The comprising: present invention as claimed further provides an absorbent structure, an acquisition layer of latex-bonded synthetic matrix fibers, said matrix fibers having a length of from about 3 to about 15 mm; (ii) a distribution layer of bonded cellulose fibers, which fibers are thermalbonded, latex-bonded, or a combination thereof, the distribution layer in fluid communication with the acquisition layer; and (iii) a storage layer comprising cellulose fibers and superabsorbent polymer particles wherein the fibers are thermally bonded, the storage layer in fluid communication with the distribution layer.
The present invention as claimed still further provides an absorbent structure, comprising: an acquisition layer comprising latex-bonded PET matrix fibers, said matrix fibers having a length from about 3 to about 12 mm and a thickness from about 6 to 15 denier, wherein the acquisition layer has a basis weight range of about 20 to about 60 gsm; (ii) a distribution layer of cellulose fibers, which fibers are thermal-bonded or chemically modified, and wherein the distribution layer has a basis weight range of about 30 to about 90 gsm, the distribution layer in fluid P:\WP!OCS\CAB\SPECI\75563.d-27O02/02 communication with the acquisition layer; and (iii) a storage layer comprising cellulose fibers and superabsorbent polymer particles wherein the fibers are thermally bonded, and wherein the storage layer has a basis weight range of about 70 to about 130 gsm, the storage layer in fluid communication with the distribution layer.
The comprising: present invention as claimed further provides an absorbent structure, 0 0 an acquisition layer of latex-bonded PET matrix fibers, said matrix fibers having a length from about 3 to about 12 mm and a thickness from about 6 to 15 denier, wherein the acquisition layer has a basis weight range of about 20 to about 60 gsm; (ii) a distribution layer of cellulose fibers, which fibers are thermal-bonded or chemically modified, and wherein the distribution layer has a basis weight range of about 30 to about 100 gsm, the distribution layer in fluid communication with the acquisition layer; and (iii) a storage layer comprising cellulose fibers and super absorbent polymer particles wherein the fibers are thermally bonded, and wherein storage layer has a basis weight range of about 250 to about 340 gsm, the storage layer in fluid communication with the distribution layer.
The absorbent structure of the invention has the following advantages: it is highly absorbent as it is made of a low-density material and has high-bulk properties; (ii) the layers are uniform due to the manner in which superabsorbent particles are deposited into the layers providing an absorbent web, and thus provide increased absorbent potential of the article; (iii) the absorbent article permits more economical means for providing an absorbent article because the function of multiple materials are combined into a single roll; and (iv) the wettability of the article can be adjusted as a result of (or by) surfactant addition during the acquisition layer forming process.
P:\WPOCS\CAB\SPEE \755463o.d-27/002J DETAILED DESCRIPTION OF THE INVENTION All patents, patent applications, and literature references cited herein are hereby incorporated by reference in their entirety.
The present invention provides an improved fibrous absorbent structure which contains a liquid acquisition layer of lower density and a fibrous storage layer of relatively higher density. The structure is a composite including at least these two layers which confer upon the structure the ability to acquire and distribute fluids through the density 10 gradient. The acquisition layer is capable of rapidly acquiring liquid from insult. The 4:.
storage layer absorbs and stores the liquid acquired from the acquisition layer.
In addition, the invention preferably contains a distribution layer, which in combination with the fluid acquisition layer provides an improved ADL, containing at least two layers, a top acquisition layer and a distribution layer. When used in a disposable :absorbent product, the acquisition layer is closer to the skin of the wearer and away from the storage layer; the distribution layer is closer to the storage layer and away from the skin "of the wearer. The acquisition layer provides rapid fluid acquisition under load. The distribution layer provides z-direction capillary force to pull fluid into the absorbent 20 storage layer, away from the skin of the wearer, to provide temporary fluid immobilization, and to act as a conduit for fluid drawn into the unsaturated portion of the storage layer.
The absorbent structure of the invention has high absorbent capacity and is particularly WO 99/63922 PCT/US99/13175 useful as an absorbent core for disposable absorbent articles such as diapers, adult incontinence pads and briefs, and feminine sanitary napkins, and the like.
The fiberized fluff cellulose fibers used in the ADL or storage layer of the composite structure of the present invention may be selected from wood cellulose such as Foley fluff, cotton linter pulp, chemically modified cellulose such as crosslinked cellulose fibers or highly purified cellulose fibers, such as Buckeye
HPF.
The present invention makes use of the unexpected discovery that a latex-bonded, synthetic fiber in the acquisition layer provides an absorbent structure having improved acquisition and retention characteristics absorbency) compared with an absorbent structure employing an acquisition layer lacking such fibers. The advantage of using synthetic fibers is that such fibers maximize the surface dryness of the absorbent product. Any synthetic fiber, including polyester fibers, such as polyethylene terepthalate (PET), polypropylene, nylon and acrylic, and combinations thereof, may be used provided that the fiber has the property of forming large pores resistant to collapse when the layer is wet.
The melting point of the synthetic fiber should be taken into consideration during the manufacturing process and the temperature should be adjusted to avoid melting of the fiber. For purposes of the present disclosure, "large pore" means a pore larger, and more resistant to collapse, than the pore formed by cellulose fibers. Because large pores contained within a synthetic fiber matrix resist collapse under pressure when wet, the top layer can rapidly acquire a surge of fluid as it passes through the liner or top sheet of the absorbent product.
The size of the pore will depend on the composition of the fiber, size of the fiber fiber diameter), resiliency of the fiber, and resiliency of the latex. A person of skill in the art may optimize the pore size to suit any particular need using general knowledge in the art (see, for example, U.S. Patent Nos. 5,569,226 and 5,505,719 issued to Cohen) and routine experimentation.
The synthetic fibers of the top layer are bonded with an aqueous dispersion (emulsion) of a natural or a synthetic polymer latex. Any latex may be used in the invention. The synthetic polymer may be, for example, a polymer or copolymer of alkylacrylates, vinyl acetate, or styrene-butadiene. Other polymers WO 99/63922 PCT/US99/13175 known in the art may be used. For purposes of industrial hygiene and elimination of a solvent recycling step, the synthetic latexes can be applied as an aqueous based emulsion rather than an organic solvent emulsion. In the present invention, the preferred matrix fibers of the acquisition layer are 3 to 20 denier crimped PET fibers with a cut length of 3 to 15 mm.
The distribution layer of the improved ADL preferably contains latex and/or thermal bonded cellulose fibers. Any fluff cellulose fibers may be used in this layer, preferably wood fibers such as airlaid-fluff cellulose, chemically modified cellulose fibers, cross-linked cellulose fibers), highly purified cellulose, cotton linter fibers, or blends thereof. For bonding purposes, the latex dispersions used for bonding the fibers of the top layer may be used. Alternatively, or in combination with a latex binder, thermoplastic fibers or powder may be used for bonding upon heating to the melting point of the thermoplastic fiber or powder. Bicomponent fibers having a PET core surrounded by a polyethylene sheath, Hoechst-Trevira Type-255 (Charlotte, NC), and polyethylene powder may be used.
The distribution layer of the improved ADL provides both a temporary retention zone and a liquid distribution channel into the final storage layer. The cellulose fibers of this layer form a microporous medium that spontaneously distributes fluid from the point of fluid insult to unsaturated portions of the distribution layer via a combination of surface tension driving force and gravity.
Once the spreading fluid from insult contacts an unsaturated portion of the storage layer, which has a higher surface tension than the ADL, the fluid within the distribution layer flows into the storage layer until a surface tension equilibrium is reached. The higher surface tension of the storage layer can be generated by providing higher density cellulose fiber and/or superabsorbent particles. Thus the distribution layer becomes both a fluid reservoir for, and a flow channel to, the storage layer. The flow channel function is particularly important in certain thin absorbent pads where the ADL covers a significantly greater surface area than the absorbent core or storage layer.
Optionally, other ingredients such as surfactants, pigments, and opacifiers may be added to the acquisition or distribution layers without affecting absorbency.
WO 99/63922 PCT/US99/13175 The basis weight of the ADL layer of the invention may range from about 30 to 150 gsm, preferably from about 60 to 100 gsm, and most preferably about 80 gsm.
In one embodiment, the basis weight of each of the acquisition and the distribution layer of the ADL may range from about 15 to 60 gsm. Preferably, the basis weight of each layer is at minimum about 25% of the total ADL basis weight. In one embodiment, the top layer is from about 25 to 50 of the total ADL basis weight.
The ADL of the present invention may contain an optional middle layer. The middle layer may contain 100% fluff cellulose and/or chemically modified cellulose fibers or have a fiber composition that is a blend of synthetic fibers and cellulose fibers.
In one embodiment of the ADL, the acquisition layer contains about 80-90% by weight of 6.7 dtex (wt/length of fiber) in size by 6 mm in cut length polyester (PET) fiber bonded with 10-20% by weight of an aqueous binder resin.
The bottom layer contains 80-90% of fiberized fluff cellulose fibers that are bonded using 10-20% of an aqueous binder. The fiberized fluff cellulose fibers may contain wood cellulose such as Buckeye Foley fluff (Buckeye Technologies Inc.), cotton linter pulp such as Buckeye HPF (Buckeye Technologies Inc.), or chemically modified cellulose such as cross-linked cellulose fibers. In another embodiment, the top and bottom layers of the ADL are as above, but a middle layer containing a blend of PET and cellulosic fibers is also present. In this embodiment the top layer is at least 10% of the total ADL weight and the bottom layer is no more than of the total ADL basis weight.
The preferred overall basis weight range of the composite absorbent structure of the invention is 100-500 grams per square meter (gsm). The composite absorbent structures include a fluid acquisition layer and a fluid distribution layer (described above) and a fluid storage layer. The fluid storage layer is below the fluid distribution layer and is comprised of a fluff cellulose or chemically modified fluff cellulose matrix fibers, a superabsorbent polymer (SAP), and a bonding element. The bonding element is preferably bicomponent fibers in the concentration of 5 to 20 but may also include thermoplastic powders.
Preferably, the SAP content is 10-70% by weight of the absorbent structure.
WO 99/63922 PCT/US99/13175 As used herein, "superabsorbent polymer" or "SAP" means any suitable hydrophilic polymer that can be mixed with fibers of the present invention.
A superabsorbent polymer is a water soluble compound that has been cross-linked to render it water insoluble but still swellable to at least about 15 times its own weight in physiological saline solution. These superabsorbent materials generally fall into 3 classes, namely starch graft copolymers, cross-linked carboxymethylcellulose derivatives, and modified hydrophilic polyacrylates.
Examples of absorbent polymers include hydrolyzed starch-acrylontrile graft co-polymer, saponified acrylic acid ester-vinyl co-polymer, modified cross-linked polyvinyl alcohol, neutralized cross-linked polyacrylic acid, cross-linked polyacrylate salt, and carboxylated cellulose. The preferred superabsorbent materials, upon absorbing fluids, form hydrogels.
The superabsorbent polymer materials have relatively high gel volume and relatively high gel strength as measured by the shear modulus of the hydrogel.
Such preferred materials also contain relatively low levels of polymeric materials which can be extracted by contact with synthetic urine. Superabsorbent polymers are well-known and are commercially available. One example is a starch graft polyacrylate hydrogel marketed under the name IM1000 (Hoechst-Celanese, Portsmouth, VA). Other commercially available superabsorbent polymers are marketed under the trademark Sanwet (Sanyo Kasei Kogyo Kabushiki, Japan), Sumika Gel (Sumitomo Kagaku Kabushiki Haishi, Japan), Favor (Stockhausen, Garyville, LA) and the ASAP series (Chemdal, Aberdeen, MS). Superabsorbent particulate polymers are also described in detail in U.S. Patents 4,102,340 and Re.
32, 649. An example of a suitable SAP is surface cross-linked acrylic acid based powder such as Stockhausen 9350 or SX FAM 70 (Greensboro, NC).
The preferred basis weight range(s) and SAP content may vary with the intended application. For feminine hygiene and light capacity adult incontinence applications, for example, the basis weight and SAP content will tend to be toward the lower end of the ranges indicated in Table 1. For infant diaper and heavy capacity adult incontinence applications, the preferred basis weight and SAP content will tend to be toward the high end of the specified range in Table 1.
Multiple matrix fibers can be used in an absorbent article of the WO 99/63922 PCT/US99/13175 invention, however, it is preferred that collectively the matrix fibers constitute most of the fibers in the material at least The term matrix fiber as used herein, refers to a synthetic or cellulosic fiber that does not melt or dissolve to any degree during the forming or bonding of an air-laid absorbent structure. The terms "thermal bonding" or "thermal" herein refer to the blending of thermoplastic material bonding methods listed in Table 1) in which the matrix fiber(s) and SAP bond the absorbent layers when heat is applied.
Examples of suitable thermoplastic materials include thermoplastic microfibers, thermoplastic powders, bonding fibers in staple form, and bicomponent staple fibers. Bicomponent staple fibers are characterized by a high melt temperature core polymer (typically polyethylene terephthalate (PET) or polypropylene) surrounded by a low melt temperature sheath polymer (typically polyethylene, modified polyethylene, or copolyesters). In the preferred embodiments of this invention, bicomponent fibers provide the means of thermal bonding.
Table 1 provides a general outline of an embodiment of the invention.
TABLE 1 Layer Matrix Fiber SAP Bonding Basis Wt Range Method (gsm) Acquisitio Polyester (PET) and/or None Latex binder 20 n polyolefin homopolymer fibers Distributio Fluff cellulose and/or None Thermal and/or 20 100 n chemically modified cellulose latex binder fiber Storage Fluff cellulose and/or 10-75 Thermal 60 400 chemically modified cellulose fiber In one embodiment for feminine hygiene and light adult incontinence products, the absorbent product of the invention contains an acquisition layer, a distribution layer and a storage layer, having a total basis weight of 120 gsm to 290 gsm. The acquisition layer, comprising latex bonded PET matrix fibers, has a to 60 gsm total basis weight. The matrix fibers are 6 to 15 denier in size, 3 to 12 mm in length and have 2 to 5 crimps/cm. The latex is an emulsion of ethylene WO 99/63922 PCT/US99/13175 vinyl acetate, styrene-butadiene, or acrylic polymer. The latex binder is about 5 to of the weight of the acquisition layer. The distribution layer, comprising thermal bonded fluff cellulose or chemically modified fluff cellulose fibers, has a to 90 gsm total basis weight. The cellulose fiber is thermally bonded with 5 to 20% by weight of sheath/core bicomponent fiber 3 denier T-255 bicomponent fiber from Hoechst-Celanese, Charlotte, NC). The storage layer of thermal bonded fluff cellulose with 20 to 50% SAP has a 70 to 130 gsm total basis weight. The fluff cellulose/SAP mixture is thermally bonded with 5 to by weight of sheath/core bicomponent fiber. Specific embodiments are described in Examples 3, 9, 14, 15, 16.
In another embodiment, which can be employed in infant diapers and heavy adult incontinence products, the acquisition layer, distribution layer, and storage layer have a total basis weight of 300 gsm to 500 gsm. The acquisition layer, comprising latex bonded PET matrix fibers, has a 20 to 60 gsm total basis weight. The matrix fibers are 6 to 15 denier in size, 3 to 12 mm in length and have 2 to 5 crimps/cm. The latex is an emulsion of ethylene vinyl acetate, styrenebutadiene, or acrylic polymer, and is about 5 to 25% of the weight of the acquisition layer. The distribution layer, comprising thermally bonded fluff cellulose or chemically modified fluff cellulose fibers, has a 30 to 100 gsm total basis weight. The cellulose fiber is thermally bonded with 5 to 20% by weight of sheath/core bicomponent fiber. The storage layer of thermally bonded fluff cellulose with 40 to 75% SAP has a 250 to 340 gsm total basis weight. The fluff cellulose/SAP mixture is thermally bonded with 5 to 10% by weight of sheath/core bicomponent fiber. Specific embodiments are described in Examples 8 and An absorbent article of the invention can be made in one continuous process utilizing air forming equipment such as equipment sold by M&J Fibertech (Horsens, Denmark) or Dan-Web (Aarhus, Denmark). The bottom or cellulose fiber layer is formed onto a moving collection wire, and the synthetic fiber layer is airlaid directly on top of the cellulose fiber layer. The resulting composite structure is then passed under an adhesive application station (typically a set of spray nozzles or foam coater) that applies adhesive directly onto the synthetic fiber layer. The material then travels through a hot air oven, or other suitable heating device, to WO 99/63922 PCT/US99/13175 bond the structure. In the preferred embodiments, adhesive is next applied to the cellulose fiber side of the composite structure and the material is passed through a second oven to dry the adhesive. A third heating station may be employed to insure that the adhesive is fully cured. The absorbent structure of the invention may be finally packaged and shipped in roll-goods form.
Preferably, the absorbent structures of the invention are prepared as an airlaid web. The composite material may be manufactured in a continuous operation provided the production line has at least three separate forming heads, a synthetic fiber dosing system capable of handling at least two different synthetic fibers simultaneously, a superabsorbent powder dosing system and a latex adhesive application system.
The airlaid web is typically prepared by disintegrating or fiberizing a cellulose pulp sheet or sheets, typically by hammermill, to provide individualized fibers. The individualized fibers are then air conveyed to forming heads on the airlaid web forming machine. The forming heads include rotating or agitated drums, generally in a race track configuration which serve to maintain fiber separation until the fibers are pulled by vacuum onto a foraminous condensing drum or foraminous forming conveyor (or forming wire). In the M&J machine, the forming head includes a rotary agitator above a screen. Other fibers, such as a synthetic thermoplastic fiber, may also be introduced to the forming head through a fiber dosing system which includes a fiber opener, a dosing unit and an air conveyor.
Where two defined layers are desired, such as a fluff pulp distribution layer and a synthetic fiber acquisition layer, two separate forming heads are provided, one for each type of fiber.
The airlaid web is transferred from the forming wire to a calender or other densification stage to densify the web, increase its strength and control web thickness. The fibers of the web are then bonded by application of a latex spray or foam addition system, followed by drying or curing. Alternatively, or additionally, any thermoplastic fiber present in the web may be softened or partially melted by application of heat to bond the fibers of the web. The bonded web may then be calendered a second time to increase strength or emboss the web with a design or pattern. If thermoplastic fibers are present, hot calendering may be employed to WO 99/63922 PCT/US99/1 3175 impart patterned bonding to the web. Water may be added to the web if necessary to maintain specified or desired moisture content, to minimize dusting, or to reduce the buildup of static electricity. The finished web is then rolled for future use.
In one embodiment Example 1) the acquisition and distribution layer are air formed independent of the fluid storage layer. The composite acquisition/distribution layer is combined with the storage layer at the converting line. This embodiment is useful for absorbent product designs where the storage layer covers a different area than the acquisition/distribution layer. Other embodiments of this type are described in Examples 11, 12, and 13.
The following non-limiting Examples further describe the invention, the scope of which is to be limited only by the claims.
EXAMPLE 1-2 To test the acquisition rate of fluid using an ADL of the invention, samples having a target basis weight of 80 gsm were formed on a laboratory air forming device. The top layer of Example 1 contained 34 gsm of 6.7 dtex, 6 mm long polyester (PET) fibers (Hoechst Trevira, Charlotte, NC) and 6 gsm of AirFiex 192 latex binder (Air Products and Chemicals, Allentown, PA). The bottom layer contained 34 gsm Buckeye Foley fluff pulp and 6 gsm AirFlex 192 latex binder. A control sample, Example 2, was prepared on the same laboratory air forming device containing a single layer having a basis weight of 80 gsm, comprising 68 gsm Buckeye Foley fluff wood cellulose fibers and 12 gsm Air Flex 192. The Foley fluff cellulose is typical of the fiber employed in conventional airlaid acquisition layers such as Vicell 6002 (Buckeye Technologies Inc.).
Each sample was placed on a two-ply Zorbcore 5901 (Buckeye Technologies Inc.), which includes a 250 gsm thermal bonded airlaid Foley fluff material containing 25% Stockhausen SX FAM 70 SAP. The ADL/absorbent core stack was covered with an 18 gsm polypropylene top sheet. Test and control samples for 3 separate measurements (each sample having the dimensions of cm x 10 cm) were prepared. Each sample was wrapped with an appropriate coverstock material and placed on the bottom fluid intake test board with the wire or carrier side facing down. The center of the samples was marked.
WO 99/63922 PCT/US99/13175 Acquisition rate evaluations were made by subjecting test samples to three consecutive 50 ml insults of 0.9% saline solution. The first insult of 50 ml 0.9% saline solution was poured into the clear addition tube of the FIT board as fast as possible, without overflowing. The time from the moment of pouring until the saline reached the test sample was measured. The stopwatch was stopped as soon as all of the saline passed from the bottom edge of the tube. The recorded time was the time required for acquisition by the top layer. After one minute intervals, the procedure was repeated with a second and third 50 ml insult.
The acquisition rate from each fluid insult was determined according to the following formula: Acquisition Rate (ml/s) volume of fluid insult (ml) acquisition time(s) The acquisition rate results are represented in Table 2 as milliliters per second (ml/s) of fluid penetration through the top sheet.
TABLE 2 Acquisition Rate ml ACQUISTION RATE ADL Fiber Core units 1 st Insult 2nd Insult 3rd Insult Composition Ex. 1 ml/sec 7.36 2.29 1.95 PET/Foley Fluff 2 ply Zorbcore 5901 Ex. 2 mi/sec 3.23 1.15 0.86 Foley Fluff 2 ply Zorbcore 5901 The results show that the sample containing the bilayer of latexbonded PET/Foley fluff the ADL prepared according to the present invention) had approximately twice the fluid acquisition rate relative to the control sample consisting of a single layer lacking PET for each of the three insults.
Another critical function of an ADL is to isolate the wearer of the absorbent product from the fluid contained within the absorbent product. While a low density airlaid cellulose layer may have very rapid fluid acquisition, the cellulose fibers of a conventional airlaid ADL often retain fluid or provide a conduit for fluid to leak out of the core when the ADL is under pressure, thus making the wearer's skin wet. In contrast, the synthetic fibers of the top layer of the present ADL create large pores so that, even under pressure, the top layer neither retains fluid nor provides a conduit for fluid to leak from the distribution or storage layers toward the wearer. This advantage is experimentally shown in the present example.
WO 99/63922 PCT/US99/13175 The test samples described in Example 1 were placed on top of a twoply Zorbcore 5901, below the 18 gsm non-woven top sheet. This stack of materials was tested according to the rewet/fluid retention test described, supra, by measuring the amount of 0.9% saline solution that could be absorbed back through the top sheet by a stack of filter paper under 0.1 psi pressure after each fluid insult.
Test and control samples for 3 separate measurements (each measuring 8 x 11") were prepared. Each sample was placed onto the plastic platform with tissue side down and its center was marked. Fifty ml of 0.9 saline solution (first insult) was drained onto the sample from a funnel from a distance of approximately above the center of the sample. The sample was allowed to sit for 20 minutes. A stack of 12 filter papers was weighed and placed on the center of the wetted area and pressed by a circular weight on top. After 2 minutes the wet filter papers were removed and weighed again. This procedure was repeated with a second insult of ml saline and a stack of 16 filter papers, and a third insult of 50 ml saline and a stack of 20 filter papers. The rewet value and the percent fluid retention was calculated for the first, second and third insults according to the following formulas: Reweti 2 3 Wet filter papers weight Dry filter papers weight Retention (50 Rewet) 50 x 100% The results are represented in Table 3 as a percentage of each 50 ml fluid insult that was retained by the core after the filter paper was removed.
TABLE 3 Fluid Retention Results ml FLUID RETENTION ADL Fiber Core 1st Insult 2nd Insult 3rd Insult Composition Ex. 1 99.46% 89.92% 63.64% PET/Foley Fluff 2 ply Zorbcore 5901 Ex. 2 97.74% 62.24% 33.96% Foley Fluff 2 ply Zorbcore 5901 The latex bonded PET/Foley fluff cellulose bilayer the ADL prepared according to the present invention) had a significantly higher fluid retention than the sample containing only latex-bonded fluff cellulose.
EXAMPLES 3-4 WO 99/63922 PCT/US99/13175 To test the absorbent core of the invention in combination (Example 3) a composite absorbent core was created by first air forming a layer of 100% 6 denier x 6 mm long PET fibers on top of preformed Vizorb X479 material (Buckeye Technologies Inc.). The PET fiber layer was then bonded in place by spraying a 15% by weight aqueous solution of AirFlex 192 latex binder (Air Products Chemicals, Allentown, The Vizorb X479 is a latex/thermal bonded absorbent core fluff cellulose that contains 30% SAP (Stockhausen SX FAM 70; Greensboro, NC). Vizorb X479 also has a SAP-free top layer containing thermal-bonded Buckeye HDF chemically modified fluff cellulose that becomes the fluid distribution layer once the latex bonded acquisition layer is formed on top of the X479 material.
A 15 gsm cellulose tissue carrier sheet was provided below the bottom surface of the Vizorb X479 material for SAP containment during the web forming process to prevent fouling of the equipment due to SAP separating from the structure. The target composition and configuration of the absorbent structure of Example 3 is shown in Table 4. This preparation was repeated using a composite absorbent core formed from a layer of 100% 6 den x 12 mm PET fibers.
The fluff cellulose fiber in the distribution and storage layers was 67% Buckeye Foley Fluff and 33% Weyerhaeuser PD 416 (Seattle, WA) by weight. The bicomponent fiber used was 3.1 dtex x 4 mm long Hoechst-Trevira T-255 (Charlotte, NC), the SAP powder was Stockhausen SX-70 (Greensboro, NC), and the latex binder resin was AirFlex 124 (Air Products). The term "dtex" refers to the mass, in grams, of 10,000 meters of fiber. The term "denier" refers to the mass, in grams of 9,000 meters of fiber.
The acquisition layer matrix fiber of Example 3a contained Hoechst- Trevira Type-224 crimped 6.7 dtex by 6 mm long polyester (polyethylene terephthalate or PET), and AirFlex 192 latex resin. Example 3b was identical to 3a except that the length of the PET fiber was 12 mm. The binder for the fluff cellulose acquisition layer was AirFlex 192 and the fluff cellulose was 100% Buckeye Foley fluff.
WO 99/63922 PCT/US99/13175 TABLE 4 Fluff Bonding Fiber SAP Powder Latex Binder PET Fiber Cellulose (gsm) (gsm) Resin (gsm) (gsm) (gsm) Acquisition none none none 6.0 34.0 Layer Distribution 30.3 3.5 none 1.3 none Layer Storage Layer 64.1 7 52.5 1.3 none A reference sample (Example 4) was created by air forming a 40 gsm layer of Foley fluff cellulose onto Vizorb X479 material. The fluff cellulose was then latex bonded as in Example 1. The reference sample exemplifies a conventional air formed structure lacking PET fiber. Table 5 shows the target composition and configuration of the reference sample.
TABLE Fluff Bonding Fiber SAP Powder Latex Binder PET Fiber Cellulose (gsm) (gsm) Resin (gsm) (gsm) (gsm) Acquisition 34.0 none none 6.0 none Layer Distribution 30.3 3.5 none 1.3 none Layer Storage Layer 64.1 7 52.5 1.3 none The test and control samples for three separate measurements were further prepared as in Example 1. Acquisition rate evaluations were made by subjecting the composite structures of Examples 3a, 3b and 4 by subjecting the samples to three consecutive insults as described in Example 1-2.
WO 99/63922 PCT/US99/13175 The acquisition rate results are represented in Table 6 as milliliters per second of fluid penetration through the top sheet.
TABLE 6 Acquisition Rate (mils) 1 st Insult 2nd Insult 3rd Insult Fiber Ex. 3a 2.27 1.05 0.58 PET (6 mm) Ex. 3b 2.13 1.12 0.68 PET (12 mm) Ex.4 0.79 0.32 0.12 Foley Table 6 shows that the samples having latex-bonded PET acquisition layer has a 300 to 400 percent greater fluid acquisition rate than the sample having a latex-bonded fluff cellulose acquisition layer.
The structures of Examples 3a, 3b, and 4 were also subjected to liquid rewet/retention testing with 50 ml saline insults as in Example 1-2. The rewet value and the percent liquid retention was calculated for the first, second and third insults according to the rewet formulas of Example 2. The results are represented in Table 7 which shows the amount of liquid in grams that could be pulled through the top sheet with filter paper.
TABLE 7 ml REWET units 1" Insult 2 n d Insult 3 r d Insult Fiber Ex. 3a grams 0.17 0.97 2.21 PET (6 mm) Ex. 3b grams 0.09 0.45 0.78 PET (12 mm) Ex. 4 grams 0.19 4.5 10.33 Foley Table 8 shows the results of Table 7 expressed as a percentage of each 50 ml liquid insult that was retained by the core after the filter paper was removed.
WO 99/63922 PCT/US99/13175 TABLE 8 ml LIQUID RETENTION 1" Insult 2"d Insult 3 rd Insult Composition Ex. 3a 99.66 98.06 95.58 PET (6 mm) Ex. 3b PET (12 99.82 99.10 98.44 mm) Ex. 4 99.62 91.00 79.34 Foley Tables 7 and 8 show that the latex-bonded PET acquisition layer yields significantly better fluid retention than a conventional latex bonded fluff cellulose acquisition layer.
EXAMPLES 5-8 In this embodiment of the invention, a layer of 6 den x 6 mm PET matrix fiber was bonded using a combination of latex bonding and thermal bonding, multibinding-a combination of two types of bonding techniques). The first step was to form an airlaid absorbent core designated DL-1. The basis weight of the DL-1 material was 425.0 gsm. The DL-1 material included a SAP/fluff cellulose fluid storage layer on a 15 gsm tissue carrier and a distribution layer which contained predominantly airlaid Buckeye HPF (chemically purified cellulose fiber having a small percentage of bicomponent fibers). The DL-1 storage layer included 144.9 gsm of fluff pulp and 153 gsm of Stockhausen 9350 SAP. The distribution layer of the DL-1 material included 48.6 gsm of Buckeye HPF fiber. In addition, 46.6 gsm of bicomponent thermal fiber was distributed throughout the core and distribution layers of the DL-1 material. The distribution layer and storage (core) layers were thermally bonded with a small amount of latex sprayed in dilute aqueous solution (17 gsm solids), such that the layers contained SAP particles and cellulose fibers.
The DL-1 material 5 was collected on a roll and a portion of the roll was passed back through an M&J web forming and bonding system (Horsens, Denmark). An acquisition layer was air formed on top of the distribution layer of the DL-1 material. For each sample, the acquisition layer was applied by blending WO 99/63922 PCT/US99/13175 the matrix fiber with the bicomponent fiber and airforming the layer onto the DL-1 material (see Table The matrix fibers Buckeye HPF and Buckeye HPZU are chemically purified cellulose fibers. The bicomponent fiber was T 255 fiber (Hoechst-Trivera). The latex was AirFlex 192 (Air Products).
TABLE 9 Ex. Matrix Fiber Basis Weight Bico Fiber Latex Total Buckeye HPF 61.6 2.8 5.6 70.0 6 Buckeye HPZU 69.5 7.2 13.5 90.3 7 cross-linked cellulose 69.3 7.2 13.5 90.0 8 H-T 6.7 dtex PET 54.6 5.2 5.2 65.0 The airlaid, multibonded structures of Table 9 were subjected to liquid acquisition rate testing according to the method described for Example 1. The results are set forth in Table TABLE Fluid Acquisition Rate (ml/sec) Multiple 50 ml Insults Ex. 1st Insult 2nd Insult 3rd Insult 6.76 2.05 1.37 6 4.46 2.03 1.39 7 5.95 2.28 1.68 8 7.69 3.79 2.81 The fluid acquisition rate of the sample material of Example 8, which contained an acquisition layer of latex bonded Polyester (PET) fibers, exhibited the highest liquid acquisition rate.
The airlaid, multibonded structures of Examples 5-8 were subjected to liquid retention testing according to the method of Example 2. The results are set forth in Table 11.
WO 99/63922 PCT/US99/13175 TABLE 11 mL Liquid Retention Ex. 1st Insult 2nd Insult 3rd Insult 96.9 57.8 39.1 6 94.5 50.9 37.7 7 98.7 65.8 52.7 8 99.8 95.2 90.3 Table 11 shows that the sample material of Example 8, which contained a PET fiber acquisition layer, had a significantly higher percentage of fluid retained under pressure in the composite structure compared with the other structures employing cellulose-based acquisition layers (Examples 5-7).
EXAMPLES 9-10 Examples 9 and 10 are specific embodiments of the three layer invention optimized for thin sanitary pads and light adult incontinence applications (Example and for infant diaper/training pant applications (Example Example 9 A sample was produced on a M&J type air forming line with a target composition and configuration as described in Table 12. The storage layer was made from Foley fluff cellulose (Buckeye Technologies Inc.) and the distribution layer from HPF fluff cellulose (Buckeye Technologies Inc.). The binding fiber employed was T-255 3 den x 4 mm (Hoechst-Trevira). The synthetic matrix fiber employed was (Type D2645 6 den x 6 mm crimped (4.2 cr/cm) PET fiber (Hoechst- Trevira). The SAP used was Stockhausen type 9350. The sample material was formed onto an 18 gsm tissue sheet to prevent contamination of the air forming equipment with particles of superabsorbent powder. This three layer structure plus carrier tissue was thermally bonded and compacted to achieve an overall material density of 0.094 g/cc and basis weight of 219 gsm. The resulting ADL/core absorbent material is one embodiment of the invention which can be used for thin sanitary pads and light adult incontinence applications.
WO 99/63922 PCT/US99/13175 TABLE 12 Fluff Cellulose (gsm) none 57 55 Bonding Fiber (gsm) none 3 5
SAP
Powder (gsm) none none 40 Latex Binder Resin Pet Fiber (gsm) (gsm) Acquisition Layer Distribution Layer Storage Layer 6.0 none none 34.0 none none The sample was tested against two commercially available America and European brand A) thin sanitary pads for both fluid acquisition and retention according to the methods of Examples 1 and 2, except that the amount of each fluid insult was 10 ml. The results are shown in Table 13. The weight basis is a sum of the multiple absorbent components that made up the fluid acquisition, distribution, and storage layers of a product.
ADL/Core Basis Wt.
(gsm) Table 13 Acquisition Rate (ml/sec) 10 ml saline insults 1" 2 d 3 rd Insult Insult Insult 4.5 2.3 1.9 3.5 0.7 0.9 0.3 0.2 Fluid Retention 10 ml saline insults Insult 2 nd Insult 3 d Insult Example 9 European
N.
American 219 240 250 Example A sample was produced in the same manner as the sample in Example 9, in accordance with Table 14, except that the fluff cellulose in the storage layer was ND-416 (Weyerhaeuser, Tacoma, WA) and the fluff cellulose in the distribution layer was Foley fluff (Buckeye Technologies Inc.). The overall material density was 0.117 g/cc and basis weight was 504 gsm.
WO 99/63922 PCT/US99/13175 Acquisition Layer Distribution Layer Storage Layer Fluff Cellulose (gsm) none 85 105 Table 14 Bonding Fiber (gsm) none 15 15
SAP
Powder (gsm) none none 180 Latex Binder Resin (gsm) 8.0 none none Synthetic Matrix Fiber (gsm) 42.5 none none Sample 1 was tested against two commercially available infant diapers and training pants for both fluid acquisition and retention according to the methods of Examples 1 and 2. The results are shown in Table 15. The basis weights of the acquisition, distribution and storage components of the commercial products were as follows: A, 622 gsm; B, 792 gsm; C, 522 gsm; and D, 840 gsm.
Table Example 10
A
B
C
D
Multiple Saline Insults Acquisition Rate 3 rd Insult 1" Insult 4.0 99.9 2.4 99.9 1.8 99.9 2.9 99.5 2.5 96.4 Multiple Saline Insults Fluid Retention 2" Insult 3 r d 50 ml Insult 97.0 87.0 96.8 79.8 99.0 95.9 96.9 87.3 79.1 57.2 EXAMPLES 11-13 These examples show three embodiments of an ADL of the invention on a preformed and bonded absorbent core (see Table 16). The embodiments compare the effect of matrix fiber size over the range of 6 to 15 denier. The distribution layer in Example 13 has a combination of latex and thermal bonding.
Example 11 The two layer ADL was formed in the same manner as in Example 1, in accordance with Table 16, using Foley fluff cellulose in the distribution layer (Buckeye Technologies Inc.), T 255 3 den x 4 mm bonding fiber (Hoechst-Trevira), AirFlex 192 latex binder (Air Products), D2645 PET 6 den x 6 mm x 4.2 cr/cm synthetic matrix fiber (Trevira) to form an 18 gsm wet laid tissue product.
WO 99/63922 PCT/US99/13175 Example 12 In this example an ADL was formed as in Example 11, except that the synthetic matrix fiber utilized in the acquisition layer was Trevira D2670 PET synthetic matrix fiber (9 den x 6 mm x 3.9 cr/in).
Example 13 In this example an ADL was formed as in Example 11, except that the synthetic matrix fiber utilized in the acquisition layers was Trevira D2660 PET synthetic matrix fiber (15 den x 6 mm x 3.2 cr/cm).
The samples from Examples 11-13 were placed over Buckeye Airlaid grade 5901 cores (Buckeye Technologies Inc.) and tested for fluid acquisition rate and fluid retention according to the methods of Examples 1 and 2. The 5901 material is a thermally bonded uniformly blended materials containing Stockhausen SX FAM 77 superabsorbent powder, 10% Trevira T-255 bicomponent fiber, 6% tissue carrier sheet, and 59% Weyerhaeuser Super Soft Ultra fluff cellulose.
The results in Table 17 show that the 9 den PET fiber employed in Example 12 provided the maximum fluid acquisition rate; fluid retention was not significantly effected by the choice of matrix fiber in these examples.
Table 16 Fluff Bonding SAP Latex Synthetic Cellulose Fiber Powder Binder Resin Matrix Fiber (gsm) (gsm) (gsm) (gsm) (gsm) Acquisition Layer none none none 4.0 22.6 Distribution Layer 37.3 15 none 8.0 none WO 99/63922 PCT/US99/13175 Table 17 Acquisition Rate (ml/sec) Multiple 50 ml Saline Insults 1" Insult 2 "d Insult 3 d Insult 14.2 6.5 5.5 Fluid Retention Multiple 50 ml Saline Insults 1" Insult 2" d Insult 3 rd Insult 71.7 87.0 89.0 Example 11 Example 12 Example 13 15.0 10.7 70.1 78.6 85.7 88.3 86.5 90.0 EXAMPLES 14-16 These Examples compare various latex bonders used in the acquisition layers. In Examples 14-16, the latex bonded PET acquisition layer was formed onto a Vizorb X479 absorbent core (Buckeye Technologies Inc.) (See Example The configuration of the absorbent samples is set forth in Table 18.
Example 14 The fluff cellulose used in the distribution layer and in the storage layer was HPF and Foley fluff, respectively (Buckeye Technologies Inc.). The bonding fiber was T-255 3 den x 4 mm (Hoechst-Trevira). The latex binder was AirFlex 192 (Air Products). The synthetic matrix fiber was Type D2645 PET 6 denier x 6 mm x 4.2 cr/cm (Trevira, Inc., Germany). Samples were formed onto 18 gsm wet laid tissue.
Fluff Cellulose (gsm) Table 18 Bonding SAP Fiber Powder (gsm) (gsm) Latex Binder Resin (gsm) 6.0 1.3 1.3 Matrix Fiber (gsm) 34.0 none none Acquisition Layer Distribution Layer Storage Layer none 30.3 64.1 none 3.5 7 none none 52.5 WO 99/63922 PCT/US99/13175 Example A second sample was produced which contained GenFlo 3060 styrene-butadiene copolymer as the latex bonder (GenCorp Specialty Polymers, Akron, OH).
Example 16 A third sample was produced which contained GenFlo 9355 styrenebutadiene-acrylic terpolymer as the latex binder (GenCorp Specialty Polymers, Akron, OH). Two percent of Aerosol OT 75 obtained from Van Waters Rodgers, Memphis, TN a surfactant, was added to the aqueous latex bonder solution to render the acquisition layer hydrophilic.
The samples were tested for fluid acquisition rate and fluid retention testing of 0.9% saline solution according to the methods of Example 1 and 2 except that the amount of each fluid insult was 10 ml. The results are shown in Table 19.
Table 19 Acquisition Rate (ml/sec) Fluid Retention ml saline insults 10 ml saline insults 1" Insult 2nd Insult 3r d Insult 1' Insult 2 n d Insult 3 rd Latex Insult Example 14 4.6 2.1 1.8 98.6 79.3 51.8 AirFlex 192 Example 15 5.6 3.3 2.3 98.8 79.8 50.3 GenFlo 3060 Example 16 7.1 2.5 4.0 99.0 79.8 50.3 GenFlo 9355 Two additional variants were made of the third sample. The first variant contained 1% Aerosol OT surfactant, and the second variant had no surfactant added to the latex bonder emulsion. Samples (2.5 square inch) were placed on a horizontal surface. A 5 ml insult of 0.9% saline was poured onto each sample. The saline solution penetrated immediately into the samples having added surfactant. In samples without surfactant, the saline insult remained pooled on top of the sample for over an hour, at which time the test was terminated.
P:\WPDOCS\CAB\SPECI75463,do-27/02/2 -27- Examples 14-16 demonstrate that the wettability of an airlaid composite structure of the invention can be adjusted at the point of manufacture, and that even with large (6 denier) synthetic fibers, a minimal level of hydrophilicity must be present in the latex resin to achieve acceptable fluid penetration.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" or "comprising" will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.
ol
Claims (8)
- 3. The fluid acquisition and distribution structure of claim 1 2 wherein the thickness of the synthetic matrix fibers is from about 3 to about denier. 1 4. The fluid acquisition and distribution structure of claim 3 .2 wherein the thickness of the synthetic matrix fibers is from about 6 to about 3 denier. .1 5. The fluid acquisition and distribution structure of claim 1 2 wherein the synthetic matrix fibers is selected from the group consisting of 3 polyethylene, polypropylene, polyethylene terephthalate, and mixtures thereof. 1 6. The fluid acquisition and distribution structure of claim 1 2 wherein the latex is selected from the group consisting of an aqueous emulsion of 3 ethylene vinyl acetate, acrylic, styrene-butadiene, or styrene-butadiene acrylic. 1 7. The fluid acquisition and distribution structure of claim 1 2 wherein the cellulose fibers are selected from the group consisting of wood 3 cellulose, cotton linter pulp, chemically modified cellulose, highly purified cellulose 4 fibers, and mixtures thereof. 28 1 MH1 fllONiON CT/US99/ 13175 SPE P s 2 6 SEP o000 1
- 8. An absorbent structure, comprising: 2 an acquisition layer of latex-bonded synthetic matrix fibers, said 3 matrix fibers having a length of from about 3 to about 15 mm; 4 (ii) a distribution layer of bonded cellulose fibers, which fibers are thermal-bonded, latex-bonded, or a combination thereof, the distribution layer 6 in fluid communication with the acquisition layer; and 7 (iii) a storage layer comprising cellulose fibers and super absorbent 8 polymer particles wherein the fibers are thermally bonded, the storageTayer 9 in fluid communication with the distribution layer. 1
- 9. The structure of claim 8 wherein the length of the synthetic matrix fibers is from about 6 to about 12 mm. S:*1
- 10. The structure of claim 8 wherein the thickness of the synthetic matrix fibers is from about 3 to about 20 denier. 9 999% 1 11. The structure of claim 10 wherein the thickness of the synthetic :2 matrix fibers is from about 6 to about 15 denier. 1
- 12. The structure of claim 8 wherein the synthetic matrix fibers are 9 selected from the group consisting of polyethylene, polypropylene, polyethylene 3 terephthalate, and mixtures thereof. 1 13. The structure of claim 8 wherein the latex is selected from the 2 group consisting of an aqueous emulsion of ethylene vinyl acetate, acrylic, styrene- 3 butadiene, or styrene-butadiene acrylic. 1 14. The structure of claim 8 wherein the cellulose fibers of the liquid 2 distribution layer and the liquid storage layer are the same or different and are 3 selected from the group consisting of wood cellulose, cotton linter pulp, chemically 4 modified cellulose, highly purified cellulose fibers, and mixtures thereof. 29 AMENDED SHEET WO 99/63922 PCT/US99/13175 1 15. The structure of claim 8 wherein the super absorbent polymer 2 particles are selected from the group consisting of polyacrylates, starch graft 3 copolymers, cross-linked carboxymethylcellulose derivatives, hydrolyzed 4 starch-acrylontrile graft co-polymers, saponified acrylic acid ester-vinyl co-polymers, modified cross-linked polyvinyl alcohols, neutralized cross-linked polyacrylic acids, 6 cross-linked polyacrylate salts, and carboxylated cellulose. 1 16. The structure of claim 8 wherein the super absorbent polymer 2 particles are surface cross-linked. 1 17. The structure of claim 8 wherein the acquisition layer has a 2 basis weight range of about 20 to about 80 gsm. 1 18. The structure of claim 8 wherein the distribution layer has a 2 basis weight range of about 20 to about 100 gsm. 1 19. The structure of claim 8 wherein storage layer has a basis 2 weight range of about 60 to about 400 gsm. 1 20. An absorbent structure, comprising: 2 an acquisition layer comprising latex-bonded PET matrix fibers, 3 said matrix fibers having a length from about 3 to about 12 mm and a 4 thickness from about 6 to 15 denier, wherein the acquisition layer has a basis weight range of about 20 to about 60 gsm; 6 (ii) a distribution layer of cellulose fibers, which fibers are thermal- 7 bonded or chemically modified, and wherein the distribution layer has a basis 8 weight range of about 30 to about 90 gsm, the distribution layer in fluid 9 communication with the acquisition layer; and (iii) a storage layer comprising cellulose fibers and super absorbent 11 polymer particles wherein the fibers are thermally bonded, and wherein the 12 storage layer has a basis weight range of about 70 to about 130 gsm, the 13 storage layer in fluid communication with the distribution layer. P:\WIDOCS\CABSPCI754630. do.27O2/O2 -31-
- 21. An absorbent structure, comprising: an acquisition layer of latex-bonded PET matrix fibers, said matrix fibers having a length from about 3 to about 12 mm and a thickness from about 6 to 15 denier, wherein the acquisition layer has a basis weight range of about 20 to about 60 gsm; (ii) a distribution layer of cellulose fibers, which fibers are thermal-bonded or chemically modified, and wherein the distribution layer has a basis weight range of about 30 to about 100 gsm, the distribution layer in fluid communication with the acquisition layer; and S 10 (iii) a storage layer comprising cellulose fibers and super absorbent polymer particles wherein the fibers are thermally bonded, and wherein storage layer has a basis weight range of about 250 to about 340 gsm, the storage layer in q, fluid communication with the distribution layer.
- 22. A fluid acquisition and distribution structure substantially as herein described with reference to the Examples. 0
- 23. An absorbent structure substantially as herein described with reference to the Examples. DATED this 27 th day of February 2002. BKI HOLDING CORPORATION By Its Patent Attorneys DAVIES COLLISON CAVE
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8845698P | 1998-06-08 | 1998-06-08 | |
| US8845598P | 1998-06-08 | 1998-06-08 | |
| US60/088455 | 1998-06-08 | ||
| US60/088456 | 1998-06-08 | ||
| US10234498P | 1998-09-29 | 1998-09-29 | |
| US60/102344 | 1998-09-29 | ||
| US09/232,783 US6479415B1 (en) | 1998-06-08 | 1999-01-19 | Absorbent structures having fluid acquisition and distribution layer |
| US09/232783 | 1999-01-19 | ||
| PCT/US1999/013175 WO1999063922A1 (en) | 1998-06-08 | 1999-06-08 | Absorbent structures having fluid distribution and storage layers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU4339199A AU4339199A (en) | 1999-12-30 |
| AU748366B2 true AU748366B2 (en) | 2002-06-06 |
Family
ID=27492227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU43391/99A Ceased AU748366B2 (en) | 1998-06-08 | 1999-06-08 | Absorbent structures having fluid distribution and storage layers |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1089697A1 (en) |
| JP (1) | JP2002517281A (en) |
| KR (1) | KR20010052649A (en) |
| CN (1) | CN1234334C (en) |
| AU (1) | AU748366B2 (en) |
| BR (1) | BR9911527A (en) |
| CA (1) | CA2334351A1 (en) |
| ID (1) | ID29458A (en) |
| NO (1) | NO20006231L (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4495405B2 (en) * | 2002-06-14 | 2010-07-07 | ユニ・チャーム株式会社 | Absorbent articles |
| JP4118640B2 (en) * | 2002-09-17 | 2008-07-16 | ユニ・チャーム株式会社 | Absorbent composite sheet and absorbent article using the same |
| AR042713A1 (en) * | 2003-01-13 | 2005-06-29 | Kimberly Clark Co | AN ABSORBENT ARTICLE FOR FEMALE HYGIENE |
| EP1504741A1 (en) * | 2003-08-07 | 2005-02-09 | The Procter & Gamble Company | Latex bonded acquisition layer having pressure insensitive liquid handling properties |
| EP1504739B1 (en) * | 2003-08-07 | 2013-01-30 | The Procter & Gamble Company | Latex bonded acquisition layer for absorbent articles |
| ES2346756T3 (en) * | 2004-06-01 | 2010-10-20 | Dan-Web Holding A/S | MANUFACTURE OF A MULTI-PATH FABRIC. |
| CN102294859A (en) * | 2011-08-01 | 2011-12-28 | 中山大学 | Moisture-absorbing material for sea water desalination and sea water desalination device |
| CN102755223A (en) * | 2012-06-20 | 2012-10-31 | 杭州珂瑞特机械制造有限公司 | Emulsion type SAP hygienic product core body and production method |
| CN105792786B (en) * | 2013-12-03 | 2019-05-07 | 易希提卫生与保健公司 | Absorbent article with acquisition layer |
| BR112017014938A2 (en) * | 2015-01-12 | 2018-03-13 | Georgia Pacific Nonwovens Llc | multilayer nonwoven acquisition material, multilayer nonwoven material and absorbent composite |
| EP3569210B1 (en) * | 2018-05-15 | 2022-04-27 | The Procter & Gamble Company | Disposable absorbent articles |
| CN112754771A (en) * | 2021-01-27 | 2021-05-07 | 诺宸股份有限公司 | Separated sanitary absorption article |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5188624A (en) * | 1990-01-16 | 1993-02-23 | Weyerhaeuser Company | Absorbent article with superabsorbent particle containing insert pad and liquid dispersion pad |
| US5728081A (en) * | 1996-07-16 | 1998-03-17 | Fibertech Group, Inc. | Absorbent composite article having fluid acquisition sub-layer |
-
1999
- 1999-06-08 KR KR1020007013882A patent/KR20010052649A/en not_active Withdrawn
- 1999-06-08 CA CA 2334351 patent/CA2334351A1/en not_active Abandoned
- 1999-06-08 ID ID20002635A patent/ID29458A/en unknown
- 1999-06-08 CN CNB99807165XA patent/CN1234334C/en not_active Expired - Fee Related
- 1999-06-08 JP JP2000552997A patent/JP2002517281A/en not_active Withdrawn
- 1999-06-08 AU AU43391/99A patent/AU748366B2/en not_active Ceased
- 1999-06-08 EP EP19990955415 patent/EP1089697A1/en not_active Withdrawn
- 1999-06-08 BR BR9911527A patent/BR9911527A/en not_active Application Discontinuation
-
2000
- 2000-12-07 NO NO20006231A patent/NO20006231L/en not_active Application Discontinuation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5188624A (en) * | 1990-01-16 | 1993-02-23 | Weyerhaeuser Company | Absorbent article with superabsorbent particle containing insert pad and liquid dispersion pad |
| US5728081A (en) * | 1996-07-16 | 1998-03-17 | Fibertech Group, Inc. | Absorbent composite article having fluid acquisition sub-layer |
Also Published As
| Publication number | Publication date |
|---|---|
| NO20006231L (en) | 2001-02-06 |
| KR20010052649A (en) | 2001-06-25 |
| CN1321075A (en) | 2001-11-07 |
| EP1089697A1 (en) | 2001-04-11 |
| CA2334351A1 (en) | 1999-12-16 |
| AU4339199A (en) | 1999-12-30 |
| ID29458A (en) | 2001-08-30 |
| NO20006231D0 (en) | 2000-12-07 |
| JP2002517281A (en) | 2002-06-18 |
| CN1234334C (en) | 2006-01-04 |
| BR9911527A (en) | 2001-10-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6479415B1 (en) | Absorbent structures having fluid acquisition and distribution layer | |
| AU761200B2 (en) | Unitary fluid acquisition, storage, and wicking material | |
| US6559081B1 (en) | Multifunctional fibrous material with improved edge seal | |
| US20030195485A1 (en) | Absorbent cores with improved intake performance | |
| US20030012919A1 (en) | High-performance absorbent structure | |
| KR20020081486A (en) | Co-apertured Systems for Hygienic Products | |
| CA2391528A1 (en) | Absorbent cores with y-density gradient | |
| JPH09117470A (en) | Absorbing article | |
| AU748366B2 (en) | Absorbent structures having fluid distribution and storage layers | |
| US20020177831A1 (en) | Personal care absorbent with inherent transfer delay | |
| ZA200403286B (en) | Cover sheet for personal care products. | |
| JPH09156013A (en) | Absorbent sheet, manufacturing method thereof, and absorbent article | |
| JP3357518B2 (en) | Absorbent sheet, method for producing the same, and absorbent article | |
| JP3644737B2 (en) | Absorbent sheet, manufacturing method thereof, and absorbent article | |
| JPH03174062A (en) | Nonwoven web and its manufacture | |
| JPH09562A (en) | Absorbent article | |
| US20050153615A1 (en) | Fibrous material with high functional particle load | |
| MXPA00012252A (en) | Absorbent structures having fluid distribution and storage layers |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) |