WO2014001487A1 - Structure absorbante collée par fusion à chaud comprenant des fibres et des particules superabsorbantes et procédé de fabrication d'une telle structure - Google Patents

Structure absorbante collée par fusion à chaud comprenant des fibres et des particules superabsorbantes et procédé de fabrication d'une telle structure Download PDF

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Publication number
WO2014001487A1
WO2014001487A1 PCT/EP2013/063595 EP2013063595W WO2014001487A1 WO 2014001487 A1 WO2014001487 A1 WO 2014001487A1 EP 2013063595 W EP2013063595 W EP 2013063595W WO 2014001487 A1 WO2014001487 A1 WO 2014001487A1
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WO
WIPO (PCT)
Prior art keywords
bond
absorbent structure
particles
bonding
fibres
Prior art date
Application number
PCT/EP2013/063595
Other languages
English (en)
Inventor
Christoph Schmitz
Original Assignee
Concepts For Success (C4S) E.K.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB201211577A external-priority patent/GB201211577D0/en
Application filed by Concepts For Success (C4S) E.K. filed Critical Concepts For Success (C4S) E.K.
Priority to EP13734372.9A priority Critical patent/EP2872096B1/fr
Priority to CN201380043750.0A priority patent/CN104602658B/zh
Priority to US14/411,889 priority patent/US10239284B2/en
Publication of WO2014001487A1 publication Critical patent/WO2014001487A1/fr

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    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/729—Textile or other fibrous material made from plastics
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/729—Textile or other fibrous material made from plastics
    • B29C66/7294—Non woven mats, e.g. felt
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/737—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined
    • B29C66/7373—Joining soiled or oxidised materials
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/80—General aspects of machine operations or constructions and parts thereof
    • B29C66/81—General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps
    • B29C66/814—General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps
    • B29C66/8145—General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps characterised by the constructional aspects of the pressing elements, e.g. of the welding jaws or clamps
    • B29C66/81453—General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps characterised by the constructional aspects of the pressing elements, e.g. of the welding jaws or clamps being made of flexible slats, flexible fins, flexible bristles or springs, e.g. coiled springs
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/80—General aspects of machine operations or constructions and parts thereof
    • B29C66/83—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools
    • B29C66/834—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools moving with the parts to be joined
    • B29C66/8341—Roller, cylinder or drum types; Band or belt types; Ball types
    • B29C66/83411—Roller, cylinder or drum types
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/80—General aspects of machine operations or constructions and parts thereof
    • B29C66/83—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools
    • B29C66/834—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools moving with the parts to be joined
    • B29C66/8351—Jaws mounted on rollers, cylinders, drums, bands, belts or chains; Flying jaws
    • B29C66/83511—Jaws mounted on rollers, cylinders, drums, bands, belts or chains; Flying jaws jaws mounted on rollers, cylinders or drums
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00—Other particular articles
    • B29L2031/48—Wearing apparel
    • B29L2031/4871—Underwear
    • B29L2031/4878—Diapers, napkins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2305/00—Condition, form or state of the layers or laminate
    • B32B2305/10—Fibres of continuous length
    • B32B2305/20—Fibres of continuous length in the form of a non-woven mat
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2555/00—Personal care
    • B32B2555/02—Diapers or napkins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/0046—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by constructional aspects of the apparatus
    • B32B37/0053—Constructional details of laminating machines comprising rollers; Constructional features of the rollers

Definitions

  • the present invention is a liquid absorbent structure comprising superabsorbent polymer, such as superabsorbent particles, which are well immobilized at least in a dry state without being restricted upon swelling.
  • superabsorbent polymer such as superabsorbent particles
  • Such structures can be used to absorb bodily exudates such as in absorbent articles such as baby diapers, adult incontinence articles, and the like.
  • the present invention is a manufacturing method for providing such structures.
  • Liquid absorbent structures are well known in the art such as for the application in absorbent articles such as baby or adult incontinence diapers, feminine hygiene articles, but also for absorbing liquids in food packages or for other liquid spills.
  • SAP superabsorbent polymers
  • such SAP are typically provided as particles.
  • such particles dislocating, either during manufacturing, storage, or use, thereby at least altering the performance characteristics of the structure if not spilling out of the structures undesirably.
  • the cellulosic fibres were at least partly removed and replaced by synthetic binder.
  • EP1199059B1 (U-C; Onishi) describes the mixing of fibres exhibiting a lower and a higher melting point such that upon application of energy a three-dimensional fibre matrix is created.
  • JP2008/125602 a structure is described wherein two types of fibres with particles intermixed are permanently bonded.
  • SAP particle accumulations in "pockets" sandwiched between webs.
  • the particles can be immobilized such as by circumscribing the pockets with bonded regions, either by adhesive means or by thermobonding, see e.g.,
  • EP1621165A1 P&G; Blessing
  • WO2012/048878 shows premetering of SAP particle accumulations and thermobonding of the webs. Even though particular and complex measures, such as specific air blower arrangement, are taken to keep the boding regions free from particles, the bonding is sensitive to such contamination.
  • SAP material As SAP material swells upon imbibing liquids, it expands in volume, which has to be reflected in the structure.
  • the present invention is an absorbent structure exhibiting an x-, y-, and z-direction and comprising
  • SAP superabsorbent polymer
  • the fibrous matrix comprising the particles is capable of increasing its overall thickness upon swelling of the SAP particles whereby the expansion force exerted by the SAP particles to the bond points is higher than the de- bonding strength of the bond points such that the bond points de-bond upon swelling of the SAP particles.
  • the bond points are essentially water-insensitive.
  • the bonding pattern of the absorbent may satisfy one or more of the following conditions:
  • the bond points have a bond point size of from about 0.1 mm 2 to about 20 mm 2 ; the bond points exhibit an aspect ratio of their long axis to their short axis of at least 1.05 to 1, preferably of at least 1.1 to 1 ;
  • the bond points exhibit an ellipsoidal shape
  • the number of bond points in the pattern is from one bond point per 9 cm 2 to 1 bond point per 9 mm 2 ;
  • the bonding pattern comprises one or more sub-pattern
  • At least two bonding patterns form a macro pattern.
  • the median pore size of the fibrous matrix is preferably such that is larger than the median particle size of SAP particles.
  • the median the pore size of the fibrous matrix may be less than 3.5 times, less than 3.3 times smaller than the median particle size of the SAP particles.
  • the fibres of the fibrous matrix may reposition upon swelling of the SAP and SAP particles may re-arrange upon swelling so as to allow non-isotropic expansion of the structure preferentially in z- direction.
  • An absorbent structure according may comprise on the basis of the weight the absorbent structure
  • meltfusionable material may be unitary with the fibres.
  • the SAP particles may be present in the absorbent structure at a local basis weight of at least 50 g/m 2 , preferably more than 70 g/m 2 , more preferably more than 100 g/m 2 , even more preferably more than 200 g/m 2 .
  • the SAP particles are preferably essentially unbonded to the fibres.
  • the fibrous matrix of the absorbent structure may exhibit a pore size gradient or the structure may comprise a cover or carrier web.
  • the meltfusionable material or the fibres of the absorbent structure may comprise material, which is thermoplastic, preferably a polyolefin, more preferably polyethylene or polypropylene.
  • the fibres of the fibrous matrix of the absorbent structure may comprise a thermoplastic material exhibiting a softening temperature higher than the one of the meltfusionable material.
  • the meltfusionable material and the fibres of the absorbent structure may be essentially unitary.
  • the absorbent structure may further comprise one or more of the following:
  • cover web(s) positioned parallel to the x-y-directionally extending surface of the structure, optionally being connected thereto, optionally by the meltfusionable bond points;
  • one or more secondary containment means circumscribing the absorbent structure x-y-directionally, preferably a circumferential bonding exhibiting a bond strength higher than the bond strength of the meltfusionable bonding points;
  • expansion aiding means preferably circumferential fold lines or pop-open - lines
  • the absorbent structure may be comprised in an absorbent article, which may further comprising one or more of the following elements:
  • liquid retention means such as liquid impermeable layers
  • chassis elements for allowing fixation of the article on a wearer.
  • the present invention also relates to a method for the manufacture of an absorbent structure, comprising
  • fibres forming a fibrous matrix having an x-, y-, and thickness or z-directional extension;
  • superabsorbent polymer (SAP) particles which are capable of exerting an expansion force upon swelling upon absorption of a liquid and which are positioned within the pores of the fibrous matrix;
  • meltfusion bond points arranged in an x-y-directionally extending bonding pattern, penetrating at least partially z-directionally through the fibrous matrix.
  • a support structure preferably in the form of a flexible helical anvil; positioning the fibrous matrix with the SAP particles on the support structure; applying energy to the absorbent structure to form meltfusion points in a predetermined pattern determined by the support structure.
  • the energy is ultrasonic energy.
  • meltfusion bond points form a distinct x-y- directional bond point pattern, preferably satisfying at least one of the following conditions:
  • the bond points have a bond point size of from about 0.1 mm 2 to about 20 mm 2 ; the bond points exhibit an aspect ratio of their long axis to their short axis of at least 1.05 to 1, preferably of at least 1.1 to 1;
  • the bond points exhibit an ellipsoidal shape
  • the number of bond points in the pattern is from one bond point per 9 cm 2 to 1 bond point per 9 mm 2 ;
  • the bonding pattern comprises one or more sub-pattern.
  • the fibrous matrix is provided as one or more prebonded web(s).
  • an embedding aiding means preferably comprising one or more of the following elements
  • the method may further comprise one or more of the following steps of
  • one or more secondary containment means circumscribing the absorbent structure x-y-directionally, preferably a circumferential bonding exhibiting a bond strength higher than the bond strength of the meltfusionable bonding points; or applying an expansion aiding means, preferably circumferential fold lines or pop- open - lines;
  • Fig. 1 A to C describe schematically the arrangement of fibres, pores and SAP particles in a structure according to the present invention.
  • Fig. 2 depicts schematically particle and pore size distribution for explaining their relative size.
  • Fig. 3A to D depict schematically process set-ups as may be suitably used according to the process aspects of the present invention.
  • structures, fibrous matrices or webs as well as process aspects are described by using Cartesian coordinates, such that the x-direction or machine direction corresponds to the length, the y- or cross-machine direction corresponds to the width, and the z-direction to the thickness.
  • pore size refers to interfibre pores, i.e. the space between fibres, regardless if the space is void or completely or partly taken by SAP particles.
  • the present invention is a liquid absorbent structure for receiving and retaining aqueous fluids.
  • an important application of the present invention relates to structures that are useful in absorbent articles such as baby diaper, adult incontinence, feminine hygiene, but also for food pads, bibs, swabs, and the like.
  • the absorbent structures according to the present invention comprise a fibrous matrix with superabsorbent polymer (SAP) particles positioned in interfibre voids or pores of the structure.
  • SAP superabsorbent polymer
  • the absorbent structure is bonded by thermofusion or meltfusion bonds, which exhibit a predetermined bond strength. Once the structure is loaded with liquids and the SAP particles begin to swell, this swelling of particles will de-bond the bonding and thusly allow the particles to further swell without being restricted by the bonding of the structure.
  • Such a structure immobilizes the SAP particles in a dry state but due to the fibres between the swollen particles also in a wet state.
  • SAP particles are held in the structure in the dry state by the meltfusion bond points as primary dry containment means and the fibres of the fibrous matrix as secondary containment means. Upon wetting, the fibres function as primary containment means, preferably supported by a circumferential fixation as secondary containment means.
  • the absorbent structures according to the present invention comprise superabsorbent polymers.
  • Superabsorbent polymers (SAP) are often also referred to as "super absorbent”, “super absorbent material”, “absorbent gelling material”, hydro gel, or “absorbent polymer material”, or “AGM”, all referring to partially cross-linked polymeric materials, which can absorb water whilst they are swelling to form a gel.
  • Suitable superabsorbent materials useful in the present invention include superabsorbent particles as are known in the art.
  • superabsorbent materials include water- swellable, generally water insoluble materials capable of absorbing at least about 10 times their weight in water. More specifically, superabsorbent materials are capable of absorbing as much as 20 times their weight in water, and more specifically 50 times, 100 times, or even up to 300 times or more their weight in water (or other aqueous medium).
  • Superabsorbent materials may be formed from organic material which may include natural materials such as agar, pectin, and guar gum, as well as synthetic materials such as synthetic hydrogel polymers.
  • Synthetic hydrogel polymers include, for example, carboxymethylcellulose, alkali metal salts of polyacrylic acid and its copolymers, polyacrylamides, polyvinyl alcohol, ethylene maleic anhydride copolymers, polyvinyl ethers, hydroxypropylcellulose, hydroxypropyl acrylate, polyvinyl morpholinone, polymers and copolymers of vinyl sulfonic acid, polyacrylates, polyacrylamides, polyvinyl pyridine, and the like.
  • Other suitable polymers include hydrolyzed acrylonitrile grafted starch, acrylic acid grafted starch, and isobutylene maleic anhydride copolymers and mixtures thereof.
  • the hydrogel polymers are suitably lightly crosslinked to render the material substantially water insoluble.
  • Crosslinking may, for example, be by irradiation or by covalent, ionic, Van der Waals, or hydrogen bonding.
  • Suitable materials are available from various commercial producer or vendors, such as the Nippon Shokubai KK (Himeji, Japan), Evonik-Stockhausen GmbH (Marl, Germany), and BASF SE (Ludwigshafen, Germany), Danson (Yixing, China), EKOTEC GmbH (Haan, Germany) and many more. It is important that the SAP particles exert forces upon swelling. Such swelling forces correlate with SAP particles ability of swelling against an applied pressure.
  • a particularly preferred superabsorbent material has an Absorption against Pressure (AAP) of at least about 20 g/g and a Saline Flow Conductivity (SFC) that is greater than about 30x 10 "7 (cm 3 seconds)/g.
  • AAP is greater than about 23 g/g, more preferably greater than about 25 g/g, as measured according to the methods described in the TEST METHODS section below
  • SFC Saline Flow Conductivity
  • These superabsorbent materials are preferably used at an average basis weight of the absorbent structure of at least about 200 g/m 2 , preferably at least about 400 g/m 2 , more preferably at least about 600 g/m 2 , averaged over a representative area of the absorbent structure. In order to maintain satisfactory flexibility, the basis weight is also less than about 2000 g/m 2 .
  • the particles preferably exhibit a particle size of between 50 and 1500 ⁇ , Often, the median particle diameter ranges between about 200 ⁇ and about 800 ⁇ .
  • Typical materials are commercially available under the trade designation SXM 9170 (EVONIK-Stockhausen, Germany) or EK-X EN 67 (EKOTEC GmbH, Germany).
  • the absorbent structure comprises meltiusionable material.
  • meltfusionable refers to materials, which at increasing temperatures become soft and plastically deformable and eventually molten, thusly being able to be deformed to bond to themselves or to other material, which may remain essentially non-molten or not plastically deformed.
  • the meltfusionable material Upon cooling, the meltfusionable material returns to an essentially solid state.
  • the solidified meltfusionable material is not tacky and exhibits no significant adhesive properties. Note that although the term “melting” as commonly used in the art includes “softening” of the thermoplastic material such that it is not truly melted to the point of liquefaction but merely to the point where the outermost surface of the thermoplastic material begins to soften and become tacky.
  • the melting point of the meltfusionable material will be less than about 190°C, and preferably between about 75°C and about 175°C. In any event, the melting point of the meltfusionable material should be no lower than the temperature at which the thermally bonded absorbent structures, when used in absorbent articles, are likely to be stored. The melting point of the meltfusionable material is typically no lower than about 50°C.
  • the meltiusionable materials can be made from a variety of thermoplastic polymers, including polyolefins such as polyethylene and polypropylene, polyesters, copolyesters, polyvinyl acetate, polyethylvinyl acetate, polyvinyl chloride, polyvinylidene chloride, polyacrylics, polyamides, copolyamides, polystyrenes, polyurethanes and copolymers of any of the foregoing such as vinyl chloridevinyl acetate, and the like.
  • polyolefins such as polyethylene and polypropylene
  • polyesters, copolyesters polyvinyl acetate, polyethylvinyl acetate, polyvinyl chloride, polyvinylidene chloride, polyacrylics, polyamides, copolyamides, polystyrenes, polyurethanes and copolymers of any of the foregoing such as vinyl chloridevinyl acetate, and the like.
  • Thermoplastic elastomers such as styrenic block copolymers; elastomeric polyolefins or blends thereof, elastomeric alloys, or other thermoplastic polyurethanes, copolyester, or polyamides can be employed, but are less preferred than materials which comprising non-elastic polyolefins, in particular polypropylene.
  • the meltiusionable material may be introduced into the absorbent structure by various ways, as long as it ensured that the materials are made available at the bond sites upon bonding.
  • meltiusionable material may be in a particulate, or fibrous, or other form like films, optionally apertured films.
  • the above mentioned bicomponent fibres may be a particular execution of such combination, wherein the fibrous matrix and the meltfusionable material are identical.
  • the meltfusionable material may be distributed homogeneously. It may be applied in a concentration gradient throughout the z-direction of the structure.
  • the meltfusionable material may also be employed in an x-y-directionally extending pattern, optionally including sub- and/or macro-patterns.
  • meltfusionable material may be added via an additional layer, such as a web, such as a non- woven or a film, on one or both x-y-directionally extending surfaces of the absorbent structure.
  • additional layer such as a web, such as a non- woven or a film
  • the absorbent structure according to the present invention comprises fibres for forming a fibrous matrix.
  • Fibre refers to a continuous or discontinuous member having a high ratio of length to diameter or width.
  • a fibre may be a filament, a thread, a strand, a yarn, or any other member or combination of these members.
  • fibres also includes fibres, which over their length appear partly molten (such as when a fibre extends through a bonding region) or which are partly molten across the cross-section of the fibres, such as when a fibre is attached only superficially whilst maintaining its fibrous shape, such as when the sheath material of a bicomponent fibre is molten, but the fibre core material not.
  • Fibres useful for the present invention may be natural ones, such as modified or unmodified cellulose fibres, or syntheticgroman made”) fibres including fibres as made from natural ingredients such as without limitation viscose / rayon.
  • Preferred materials for synthetic fibres are thermoplastic materials, such as described hereinbefore for meltfusionable materials.
  • suitable thermoplastic fibres can be made from a single polymer (monocomponent fibres), or can be made from more than one polymer (e.g., bicomponent fibres).
  • bicomponent fibres refers to thermoplastic fibres that comprise a core fibre made from one polymer that is encased within a thermoplastic sheath made from a different polymer. The polymer comprising the sheath often melts at a different, typically lower, temperature than the polymer comprising the core. As a result, these bicomponent fibres provide thermal bonding due to melting of the sheath polymer, while retaining the desirable strength characteristics of the core polymer.
  • Suitable bicomponent fibres for use in the present invention can include sheath/core fibres having the following polymer combinations: polyethylene / polypropylene, polyethylvinylacetate / polypropylene, polyethylene / polyester, polypropylene / polyester, copolyester/polyester, and the like.
  • Suitable fibres may be limited length fibres, such as knows as staple fibres, but also natural fibres like cellulose fibres. Typically such natural or staple fibres exhibit a fibre length from about 0.1 to 15 cm. often from about 2 to 7 cm.
  • Suitable fibres may be substantially continuous fibres, which are not cut from their original length prior to being formed into a nonwoven web or fabric or are otherwise integrated into the absorbent structure.
  • Substantially continuous fibres may have average lengths ranging from greater than about 15 centimetres to more than one meter, and up to the length of the web or absorbent matrix being formed.
  • Spunmelt fibres are made into a fibrous matrix in one continuous process. Fibres are spun and then directly dispersed into a fibrous matrix or web by deflectors or can be directed with air streams thereto. It should be noted that the term compassionspunmelting” includes different methods such as spunbonding, meltblowing, or advanced meltblowing, referring to techniques combining elements of spunbonding and meltblowing (see e.g. BIAX ® fibres). Spunmelting may provide essentially endless fibres, such as resulting from the spunbonding process, or fibres exhibiting a limited length, such as resulting from the meltblowing process with a fibre length of typically 30 mm to about 100 mm or more.
  • the fibres useful in the present invention may generally have a thickness ranging from about less than about 1 to over 15 dTex. Usually the dTex of the fibres will range between about 1.5 and 7, though finer or even nano-fibres may be included.
  • Suitable fibres may be crimped and have a crimp count of at least two crimps per centimetre and a percent crimp of at least about 15%, preferably at least about 25%. Percent crimp is defined as the difference between the uncrimped length of the fibre (measured after fully straightening a sample fibre without stretching it elastically or plastically) and the crimped length (measured by suspending the sample fibre with a weight attached to one end equal to 2 mg per decitex of the fibre, which straightens the large-radius bends of the fibre) divided by the crimped length and multiplied by 100.
  • Crimped fibres may be staple fibres or result from a process such as spunmelting.
  • the fibres may be laid down to form a fibrous matrix in-line, i.e. during a continuous process during which the absorbent matrix is formed.
  • the fibrous matrix may be provided as a preformed and/ or prebonded web.
  • web material refers to a material, which is essentially endless in one direction, i.e. the longitudinal extension, or the length, or the x-direction in Cartesian coordinates relative to the web material. Included in this term is an essentially unlimited sequence of pieces cut or otherwise separated from an essentially endless material.
  • the web materials will have a thickness dimension (i.e. the z- direction) which is significantly smaller than the longitudinal extension (i.e. in x- direction).
  • the width of web materials (the y-direction) will be significantly larger than the thickness, but less than the length. Often, though not necessarily, the thickness and the width of such materials is essentially constant along the length of the web.
  • the web may be a "nonwoven" material that is a manufactured sheet or web of directionally or randomly oriented fibres which are first formed into a batt such as by meltblowing, spunbonding, spunmelting, solvent spinning, electrospinning, carding, film fibrillation, melt-film fibrillation, airlaying, dry-laying, wet laying with staple fibres, and combinations of these processes as known in the art.
  • the nonwoven may be consolidated and pre-bonded together by friction, such as resulting from hydroentangling or needlepunching, cohesion, adhesion or meltfusion bonding, such as between connecting points of neighbouring fibres molten by air-trough bonding, or one or more patterns of bonds and bond impressions created through localized compression and/or application of pressure, heat, ultrasonic or heating energy, or a combination thereof.
  • the basis weight of nonwoven fabrics is usually expressed in grams per square meter (gsm).
  • the use of hot-melt adhesives for pre-bonding is less preferred, if their melt behaviour interferes with the meltfusion bonding as described herein below.
  • the fibrous matrix may also be provided by fabrics which are woven, knitted, or stitch- bonded with yarns or filaments, although this may be less preferred if such structures exhibit their typical x-y- directional inhomogeneity.
  • Such in-line or pre-formed webs should satisfy the general requirements of materials being useful in absorbent structure and - where required - in disposable absorbent articles.
  • the fibrous matrix comprises resilient materials, which also exhibit low tendency of "cold flow".
  • Preferred materials comprise polyester and/ or co-polyester.
  • the structure may comprise different types of fibres in mixed or in a layered arrangement. It is important that the fibrous matrix exhibits a pore size sufficiently large to accommodate SAP particles. The pore size requirement is dependent on the particle size of the corresponding SAP particles. Considering that the SAP particle size should range between 50 and 1500 ⁇ the pores of the web preferably are adapted thereto and cover a range of up to 1500 ⁇ , but the skilled person will readily realize that not all of the pores need to be that large.
  • a simple criterion for assessing if the pores size and particle size requirements are met is to visually inspect the structures by the naked eye, magnifying glasses or a microscope. If an unloaded web and pure SAP particles are available, a representative sample of the SAP material may be sprinkled over the web at a basis weight ratio of about 70 % SAP to 30% web material.
  • SAP particles are positioned within the pores of the matrix. If appropriate measures are taken, such as recycling of material or use of cover and/or carrier materials, some of the SAP particles, in particular larger sized particles, may rest on top of the matrix, i.e. do not penetrate into the matrix, or other SAP particles may penetrate through the matrix.
  • the pore size of the web has to be considered as the pores between the fibres, i.e. neglecting the particles therein. This can be assessed by optically analysing the composite of fibres and SAP particles in the dry state, such as described in: Digital Image Analysis to Determine Pore Opening Size Distribution of Nonwoven Geotextiles; Aydilek et al.; DOI: 10.1061/(ASCE)0887-3801(2002)16:4(280).
  • the dry particles can be gently removed from the fibrous matrix, and the matrix may be analyzed optically or by other well known pore size determination methods for non-woven materials, such as wetting methods.
  • the pore size can be determined by assessing the web prior to the adding SAP particles by conventional tools, such as the digital method or fluid wetting methods. A further method can then be applied by selecting several cuts of particles exhibiting a narrow particle size, such as by selecting sieve fractions from a conventional sieve test and observing certain fraction to be retained on the surface of or penetrating through the fibrous matrix.
  • a pre-formed web may be provided with a first pore size that is modified just prior to or after the application of the SAP, such as by tentering or incremental stretching.
  • the fibrous matrix may comprise regions exhibiting varying pore size distributions.
  • there is a z-directional pore size gradient such as by gradually layering different fibre types, such as exhibiting different fibre thickness (or decitex). Varying ore size distributions may also be achieved by layering of two or more fibrous matrices.
  • the pre-formed web is not overly strong pre-bonded. Without wishing to be bound by a theory it is further believed that the fibres in the web should preferably be repositionable relative to each other and to the SAP particles.
  • Such a repositioning may take place upon the swelling of the SAP such that the particles rearrange themselves in a non-isotropic manner, which requires that the fibrous matrix respectively the fibres therein provide sufficient flexibility.
  • Such an effect can be achieved by various approaches, which may be applied alone or in combination, such as by using crimped fibres, exhibiting preferably more than about 2 crimps / cm and/ or by employing long fibres of at least 5, preferably more than 10 mm length.
  • a preferred thermoplastic nonwoven can be made of staple fibres, most preferably of staple fibres with a staple length in a range from 5 to 150 mm, most preferably 30 to 100 mm, such as crimped polyester / bicomponenet polyester at a basis weight of from about 20 gsm to about 200 gsm at a density of from about 20 to about 100 kg/m 3 .
  • Suitable materials are commercially available air-through bonded polyester materials, such as Paratherm Loft VTF 273 at 90 gms basis weight from Libeltex, Belgium, or from TEXSUS SPA, Italy.
  • the absorbent structure according to the present invention comprises SAP particles positioned in a matrix of fibres and bonded by meltfusion bonds.
  • the fibrous structure may only be bonded by the meltfusion bonds holding the particle loaded structure together.
  • the fibrous structure may be formed in-line and may be a pre- bonded web, such as by a further meltfusion bonding, such as compression or calender bonding, or by other means such as air-through bonding, resin bonding and the like.
  • the absorbent structure may have an essentially homogenous composition, i.e., the SAP in the meltfusionable material may be evenly distributed among the fibrous matrix.
  • meltfusionable material may be incorporated in the fibres of the fibrous matrix, such as when the fibrous matrix is made of meltfusionable material, or it comprises bicomponent fibres comprising meltfusionable material.
  • the absorbent structure may have a layered structure.
  • the meltfusionable material may be provided as a separate web, such as a carrier or cover web, often as a nonwoven or in a film form.
  • the cover and/or carrier web may provide meltfusionable material, but it may also function for retaining the SAP particles in the absorbent structure.
  • the cover or carrier web is a nonwoven material, such as a carded, wet- or airlaid web, or a melts-spun web, which may be a single layer or which may comprise several layers of melt-spun, spunbonded, and / or melt-blown webs, and may be denoted as "SMS", “SMMS”, SSMMS, ... webs, wherein “S” stands for spunbonding and "M” for melt-blowing.
  • cover or carrier webs exhibit a pore size so as to prevent SAP particles to penetrate through.
  • the fibrous matrix may comprise two different webs, optionally both prebonded, which optionally exhibit a different pore size or composition.
  • the SAP particles may then be arranged at different concentrations optionally segregated in particles size.
  • the absorbent structure may also have gradients of concentrations of the materials.
  • the fibrous matrix may exhibit a pore size gradient, and the SAP particles may have a corresponding concentration profile.
  • the absorbent structure may further comprise combinations of the above.
  • the SAP particles may be arranged in separate layers, e.g. one oriented from a first fibrous matrix towards the cover web, and another one oriented from a first or a second fibrous matrix towards the carrier web.
  • meltfusionable material there is sufficient meltfusionable material present to allow meltfusion bonding.
  • sufficient refers to either sufficient meltfusionable material allowing bonding regions of this material being formed.
  • sufficient may also describe the situation that the meltfusionable material connects fibres of unmolten material to each other or to other meltfusionable or not melt fusionable material.
  • meltfusionable material often more than 10% in the absorbent structure.
  • meltfusionable material and the fibrous structure may be unitary, and then all weight percentages apply to the unitary matrix providing meltfusion and fibrous material.
  • the amount of meltfusionable material should not exceed 50%, preferably not 40%> of the absorbent structure.
  • the absorbent structure may comprise more than 60%>, preferably more than 70%), often more than 80% or even more than 90% of SAP.
  • the local basis weight of the SAP particles should be sufficiently high so as to allow repositioning of the SAP particles upon swelling. As will be discussed herein below, this would not be satisfied, if - for example - less than a monolayer of materials would be introduced, as these would only swell to about three or four times their z-directional thickness and not de-bond the bond points. Once having more than a monolayer of swollen material, the swelling will reposition the particles in the fibrous matrix predominantly z-directionally, thusly increasing the thickness over proportionally and thusly easing the de-bonding.
  • the particles should be arranged exhibiting more than a "monolayer" structure, and preferably form multi-layer structure as may be expressed in terms of number of overlaying particle layers, or may be expressed by a local or an averaged basis weight, referring to the weight of particles for a given unit area.
  • a "local" basis weight will need a certain amount of averaging, which should be made over an area of 25 mm 2 .
  • the basis weight distribution may be approximated by a smoothed curve over several local determinations.
  • Both local and average basis weights for the SAP particle should not be less than about 50 g/m 2 , preferably be more than 50 g/m 2 , typically be more than about 150 g/m 2 , though often also more than 400 g/m 2 or even beyond 800 g/m 2 .
  • the basis weights should not be more than about 2000 g/m 2 .
  • the absorbent structure may have in the x-y-extension homogeneous composition and properties or it may form regions with varying composition or properties. These regions may have sharp limits or the transition may be gradual.
  • an absorbent structure is part of an absorbent article and may have different absorbency properties in one region as compared to another, such as when less absorbent capacity is positioned in the waist regions of a diaper than compared to the crotch region.
  • subsequent regions with high absorbency for forming the absorbent core of the articles may be separated in machine direction by regions with very low or even essentially no absorbent capacity.
  • an absorbent structure may comprise sub-regions, or several structures may form macro-structures.
  • the absorbent structure according to the present invention further comprises meltfusion bonds, i.e. it comprises bonding of the fibres of the fibrous matrix by molten material. It is a particular feature of the present invention that the meltfusion is executed in discrete bond or bonding regions, also interchangingly referred to as bond points. In the bond regions, the meltfusionable material is molten or at least sufficiently softened so as to allow plastic deformation. In this bond region, the fibrous matrix material is compressed so as to exhibit a smaller calliper or thickness than the surrounding region.
  • the bond region may comprise a transition region, as a transition from the centre region to the surrounding region of the fibrous matrix which is not being consolidated the same way as the bond region.
  • the thickness / calliper of the web increases from the centre region to the surrounding region, whilst the local density decreases accordingly.
  • the bond region exhibits a certain geometric extension, both with regard to the x-y- dimensions of the web, as could be seen in a x-y-top view of the web and to the z- directional dimension, as can for example be seen in a cross-sectional cut along the thickness direction of the web.
  • the bond regions exhibit x-y-directionally an elongated shape with an aspect ratio of their long axis to their short axis of at least 1.05 to 1, preferably of 1.1 to 1, and even up to 200: 1.
  • the shape is elliptical, more preferably non-circular in the top view.
  • the bond point may exhibit at least partially elliptically shaped boundaries.
  • the major or longer axis of the ellipse may be aligned with any major direction of the web, though in a particular embodiment the axis may be at an angle of more than 0° and less than 45° to the machine directional axis of a web. Whilst geometrically strictly speaking also circles represent a special form of an ellipse, they are less preferred.
  • bond regions form one or several readily recognizable repeating pattern(s).
  • a row of regions is a group of regions that are arranged predominantly along the cross-direction, whilst in a column the group of regions is arranged predominantly along the machine direction.
  • "predominantly” refers to the situation, that the projection of a characteristic line onto one direction is larger than onto the other direction perpendicular thereto.
  • Such patterns may also be formed independently of each other and then often have no direct correlation to each other, such as when a web already having a pre- bonding pattern of any kind is submitted to a process according to the present invention, or if a web is treated twice in subsequent process steps according to the present invention.
  • Such pattern may also comprise sub-patterns and or may be part of a macro-pattern.
  • the absorbent structure may exhibit a pattern over its entirety.
  • the absorbent structure may comprise two or more patterns over its entirety.
  • the absorbent structure may exhibit sub-pattern or a pattern which may be a sub pattern to a macro-pattern.
  • a bond point may be used for bonding or consolidating components of fibrous matrix. Also, bonding may be performed between strata or layers of one or more fibrous matrices, such as when spun-laid or melt blown layers are positioned on each other or on a layer of carded staple fibres, bonding can be achieved across all or some of these layers or strata. Similarly, bonding may be achieved between two or more webs, which may differ in at least one property, such as a film and a fibrous matrix. Further, the process according to the present invention may create an aperture in one of the layers but a bond point in one or preferably two enveloping fibrous matrices.
  • the preferred bonding process according to the present invention provides structures exhibiting improved tactile softness. Without wishing to be bound by the theory, it is believed, that this improvement results from the gradual transition of a fibrous structure around the bond regions to the molten centre of the regions.
  • the present invention allows to create very specific bonding patterns by modifying one or more of the following parameters of the bonding pattern
  • - size and shape of bonding points i.e. length, width and aspect ratio; - length / width distance, which may be uniform or not;
  • the area of individual bonding points is preferably less than less than about 30 mm 2 , but more than 0.1 mm 2 . If a bonding point comprises sub-regions, these numbers refer to the area circumscribing these subregions.
  • the bond point size will depend also on the thickness and amount of fibres, i.e. when less and larger fibres are employed, the bond points will preferably be larger, whilst for finer and more fibres the bond points can also be smaller.
  • the bonding points exhibit an aspect ratio of their long axis to their short axis of at least 1.05 to 1, preferably of 1.1 to 1, and even up to 200: 1.
  • the long axis of the bonding points is positioned such that its smallest angle to the pattern line is an angle of less than 90°. In case of a curvilinear pattern line, the angle is determined versus a tangent of the pattern line in the bonding point centre.
  • the distance of the bonding points along the pattern line may be less than about half a millimetre or more than 50 mm, depending on the desired degree of barrier function of the bonding pattern and/or the immobilization function with regard to the free flowing material.
  • the number of bonding points per area may be between one bonding point per each 9 cm 2 to one bonding point per each 9 mm 2 .
  • the bonding points may be formed by conventional means, such as adhesive application or meltfusion bonding. A particular execution is achieved by heat- or melt- fusing the webs together.
  • the webs are guided through a gap formed by a pair of anvils whilst or after the temperature of at least one, often of both of the webs is or has been raised by an energy source to the softening, often the melt temperature of the meltfusionable compound.
  • an energy source to the softening, often the melt temperature of the meltfusionable compound.
  • the softened or molten compounds form the bonding points.
  • Energy sources may be alone or in combination:
  • a preferred execution is sonic, more preferably ultrasonic energy emitted by a "sonotrode", optionally a rotating sonotrode, such as described in US20050034820 (Herrmann Ultraschall, Schneider).
  • the pair of anvils is made of an energy source and a counter acting anvil, though the distinction between “energy source” and “anvil” may in some instances be blurred, such as when two non-heated anvils are forming the gap and the energy has already been transferred to the web(s) or is induced by pressing the anvils together.
  • the term “counteracting” should not be seen limiting, but rather also to encompass the situation of the energy source being the first anvil and essentially stationary and the second "counteracting" anvil being moveable.
  • the "second" one of the anvils is the support system for the fibrous matrix and this is considered as the “counteracting” anvil.
  • the opposed “first” anvil is the energy source, whilst at least some of the energy may also come through the first web support system, or from another energy source.
  • a particular execution of the present invention employs bonding by using an ultrasonic bonding process employing a flexible anvil, such as described in co-pending patent publication WO2012/041055 (C4S, Schmitz).
  • a particular execution of the present invention employs bonding pattern as described in co-pending application GB1216670 (C4S, Schmitz, unpublished). To both of these applications express reference is made.
  • the absorbent structure according to the present invention should not restrict the swelling of the SAP particles unduly.
  • meltfusion bonding such that it exhibits a predetermined bond strength that is sufficiently high to withstand manufacturing, transport, pre-wetting, and in-use mechanical stress whilst being sufficiently low to de- bond upon swelling of the SAP particles.
  • the meltfusion bonding system is configured to de-bond at an applied load which is less than a load which would induce destructively tearing of the material.
  • meltfusionable material as absolute amount respectively basis weight and relative to fibres and to SAP particles;
  • the bonding pattern i.e. bonding point size / shape and the bonding point pattern (points per area unit; orientation, etc. );
  • the bonding point may have a z-directional strength profile, e.g. the bonding may not reach z-directionally completely through the structure but may only meltfusion bond certain regions. Whilst it is believed that when employing the particular bonding mechanism with flexible, such as helical anvils, this will per se result in bonding regions that are essentially free of particulate SAP, small amounts thereof may be present in the bonding regions. This is less preferred because the bond strength may exhibit a greater variability from one point to the next, but also as the tight fixation of the SAP particle in the bond point might reduce its absorbency.
  • the meltfusion bonding compresses the fibrous matrix with SAP particles embedded therein to form the bonding regions.
  • the material density in the bonding regions is increased, possibly up to the polymer density of the materials, i.e. the material is completely compressed and solidified.
  • the fibrous matrix between two respectively directly neighbouring bonding points may remain essentially uncompressed or may be compressed somewhat, but to a lesser degree than in the bonding regions.
  • the result is a x-y- directional pore size gradient - smaller or essentially non-existing at the bond points, and larger between the points, optionally gradually increasing with distance to the bonding regions.
  • Such structures may then exhibit a quilt- like form.
  • Fig 1 A schematically depicts a fibrous matrix 110 with fibres 120 and pores 130 between these fibres.
  • Fig. IB further shows dry SAP particles 140 embedded in the pores.
  • a bonding region 200 is indicated wherein the pore size appears reduced.
  • the structure exhibits a z-directional thickness 150 and a certain x- or y-directional extension is indicated by line 160.
  • Fig. 1 C the structure is schematically represented after wetting and respective swelling. As the structure swells predominantly z-directionally, as indicated by significantly increased thickness 150'and the fibres reposition as well as the swollen particles 140', which also swell into the de-bonded regions 200'. As indicated, there is only a slight change in the respective x- or y-directional extension 160'. It is further contemplated that the structure may further be compressed reversibly or at least not non-reversibly after being bonded.
  • This may be achieved by compressing the structure between smooth or patterned calender rolls at a temperature sufficiently low to not allow melting or plastic deformation of the materials, such as when compressing the structure in order to achieve lower thickness when combining the structure into an article, such as - without intending any limitation - a diaper.
  • the use of resilient fibres is preferred.
  • the volume of such particles will increase in the order of magnitude of the cube root of their capacity, if for a first approximation the shape will be assumed to be spherical.
  • the maximum pore size is larger than the maximum particle size of the SAP particles.
  • the median pore size is preferably larger than the median particle size of the dry SAP particles.
  • the porous structure may have a z-directional pore size gradient, such that larger particles may be restrained in zones with larger pores and smaller particles in zones with smaller pores.
  • the absorbent structure according to the present invention may be an essentially homogeneous web in x- and y- direction.
  • the absorbent structure may also be in the form of a macro-pattern, such as formed by sub-patterns extending in the x- and y- direction.
  • such sub-structure may correspond to an absorbent core or an absorbent article, and the absorbent structure may be a repeating series of such substructures.
  • the absorbent structure may exhibit a quilted form, whereby the structure shows indentations corresponding to the bonding points whilst the fibrous structure between the bonding points forms pillow like structures.
  • An absorbent structure according to the present invention may comprise further elements.
  • the structure may comprise more than the one cover sheet, for example one on each of the x-y-directionally extending surfaces.
  • Such additional cover sheets may also serve to retain parts of the absorbent structure in a wet state and after the meltfusion bonds are released and thus function as a secondary containment means in addition to the primary ones of containing the SAP particles in the meltfusion bonded fibrous matrix.
  • the structure may further comprise liquid handling enhancement means, as may provide preferential x- and/or y- directional liquid distribution, or an interim liquid storage capability that enables to receive liquid such as upon a urine gush, but also to release this liquid to the SAP so as to provide surge capacity for a subsequent liquid gush.
  • liquid handling enhancement means as may provide preferential x- and/or y- directional liquid distribution, or an interim liquid storage capability that enables to receive liquid such as upon a urine gush, but also to release this liquid to the SAP so as to provide surge capacity for a subsequent liquid gush.
  • the absorbent structure or its sub-structures may have further secondary containment means, such circumferentially extending intermittent or continuous bonding, which may exhibit a bond strength higher than the one of the bond points in the structure. This may also result in confining the absorbent structure in its x- and y- directional expansion upon wetting.
  • the absorbent structure may have secondary expansion aids to allow retaining of the materials of the absorbent structure without restraining the swelling of the SAP.
  • Such secondary expansion aids may be circumferential folds with intermittent or continuous bonds, that may de-bond upon a certain expansion pressure of the absorbent structure, in analogy to the meltfusion bonds, or which may de-bond by mere wetting, in analogy to the mechanisms as described in US5411497 (KC, Tanzer).
  • Such an expansion aid may also be a tear- line in an enveloping sheet, e.g. an intermittent "perf n pop" or "pop-open” cut line.
  • the fibrous matrix bonded by the meltfusion bond points serves as the primary containment means by immobilizing the dry unswollen SAP particles within pores of the fibrous structure.
  • the arrangement of the bond points being arranged in a particular and predetermined pattern and being surrounded by unbonded regions will provide a quilted structure, wherein the bond points form depressions and the unbonded regions pillow-like elevations.
  • a secondary dry containment means may be provided in the form of an additional layer of web material, such as a cover web.
  • an additional layer may follow the quilted structure, or may lay flat over it, i.e. touching the bonded matrix at the elevated regions whilst bridging the bond point depressions.
  • This quilting also provides a further density gradient in the structure, which is believed to further enhance the good liquid distribution properties of the structure.
  • the embedding of the SAP particles in the fibrous matrix provides a structure exhibiting a good touch, for examples softer as compared to sandwiched SAP pocket structures.
  • SAP particles Upon wetting of the absorbent structure the SAP particles will start swelling. As the absorption speed of SAP is relatively slow, liquid still can be distributed through pores of the fibrous matrix that are essentially free of SAP particles but also through void spaces between the fibres and the particles, further aided by the pore size gradient resulting from the quilting effect around the bond points.
  • the particles as well as the fibres of the fibrous matrix will rearrange their position relative to each other.
  • swelling force is the capability of a SAP particle to exert a force against a restraining counter force upon swelling.
  • the swelling force will be omni-directional, i.e. have force components or vectors in all three Cartesian directions. Without wishing to be bound by the theory, it is believed that this swelling force correlates to the ability to absorb liquid under pressure, which may be assessed by determining the absorption under pressure as described in the test method section.
  • the particles When several SAP particles are arranged in a close relative position to each other, the particles may restrain the swelling of neighbouring particles.
  • a monolayer of unswollen i.e. dry SAP particles positioned in a touching relationship on a flat surface is considered.
  • the interparticle voids may be filled by the swollen gel.
  • the particles Upon further swelling by provision of further liquid, the particles may stop swelling in particular for SAP of low gel strength, absorbency under pressure, or Saline flow conductivity (SFC).
  • SFC Saline flow conductivity
  • modern SAP particles exhibiting higher gel strength, absorbency under pressure and SFC values will continue to swell, and the swelling forces will result in repositioning of the particles.
  • the ability to create a z- directional force can be determined by positioning particles in a circumferentially confined space, allow the swelling by providing liquid, such a 0.9 % saline solution, and monitoring the swelling pressure that the particles may exert against a lid positioned on top of them. This ability to exert a force is also important in the present context for the de-bonding of the meltfusion bonds.
  • the mechanism is very similar to the one described in the above. When dry, the particles may be separated by fibres of the fibrous matrix, or may be in direct contact with neighbouring particles. Upon initial swelling, the spaces between particles and/or fibres are filled.
  • the neighbouring particles are a hindrance for further swelling.
  • the structure exhibits a relatively large x-y- extension and exhibits due to the bonding point pattern a relatively high resistance to x-y- directional repositioning.
  • z-directional repositioning of the swelling particles is less restrained - at least in regions sufficiently distant from bonding points, as in the proximity of these the meltfusion bonding also restricts the z-directional expansion.
  • the isotropic swelling force of the SAP particles will be re-directed into a z-directional expansion force.
  • This force is now transmitted via the fibrous structure, optionally supported by carrier or cover webs, to the bonding points and creates a pull force at each of the points.
  • this pull force acts in an abutting mode on the bonding point, which results in less strength of the bond as compared to an overlap mode, which is the predominant force transmission mode for a dry structure, where typically higher forces are transmitted along the x-y- direction.
  • meltfusion bonds can de-bond one after the next depending on the availability of the liquid. If the meltfusion bond strength is not homogeneously executed in the z-direction, such a bonding point may give consecutively in the z-direction, depending on the direction from where the liquid is provided.
  • the SAP particles Upon sufficient wetting, the SAP particles swell and because of the particular execution of the bonding points de-bond the bonds. The particles are now immobilized by the fibres of the fibrous matrix as the primary wet containment means.
  • the fibrous matrix provides a dual functionality of both dry and wet immobilization of SAP particles. It also functions as secondary wet containment means, and it may further enhance the integrity of the structure.
  • secondary containment means may function z-directionally, such as cover webs, or laterally, such as connection lines positioned outwardly of SAP particle loaded regions of the structures.
  • the absorbent structure may be regioned or have a certain limited x- and/or y- directional extension, in which the SAP particles are deposited and where the meltfusion bonding points form a pattern, x- and/or - y-directionally positioned or circumscribing connecting lines or regions are formed such as connecting cover or carrier webs extending from the primary absorbent structure outwardly.
  • the circumscribing connecting is positioned and/ or executed such that it does not limit the swelling of the SAP particles.
  • the connecting may be positioned sufficiently away from the particle containing and swelling regions whilst the region between the connecting and the swelling regions is essentially unconnected, or only weakly connected, or in a way that de-bonds upon wetting.
  • the absorbent structure may comprise one or more cover or carrier web(s) connected to the x-y- extending surface of the outside of the structure, which may comprise expansion aids, such as a fold or a pop-open tear line, which may be activated upon wetting or upon exertion of a swelling force.
  • the connecting region may comprise a expansion aid, such as an unconnected, only weakly or wetting releasably connected fold, for example a Z-fold, which extends z-directionally upon the swelling of the SAP.
  • a expansion aid such as an unconnected, only weakly or wetting releasably connected fold, for example a Z-fold, which extends z-directionally upon the swelling of the SAP.
  • Absorbent structures according to the present invention may be employed in a wide range of articles and products, such as meat pads, bed pads and the like, or as a preferred application in absorbent articles, such as baby or adult incontinence articles, feminine hygiene articles and the like.
  • absorbent structures such as baby or adult incontinence articles, feminine hygiene articles and the like.
  • it may be desirable to have a region of the absorbent structure that corresponds to an absorbent core of an absorbent article which corresponds to the meltfusion bonding pattern described herein.
  • a series of such absorbent structures may form a macro pattern or regions of subsequent patterns or regions.
  • the absorbent structure may optionally comprise sub- patterns, or differently patterned regions, for example regions corresponding to the crotch region of a wearer during use being differently patterned and optionally comprise different compositions or properties.
  • the articles may further comprise elements as usually employed in such articles, such as
  • liquid handling elements as may be provided separately to or integral with elements already described, i.e. the porous matrix for receiving the SAP particles, and/or the carrier or cover webs, as applicable;
  • liquid retention means such as liquid impermeable layers
  • the present invention is a method for manufacturing absorbent structures comprising a fibrous matrix and SAP particles embedded therein, which is bonded by meltfusion bond points.
  • the process comprises the steps of providing a fibrous matrix, meltfusionable material and SAP particles.
  • the SAP particles are positioned within the interfibre pores of the fibre matrix.
  • a bonded absorbent structure is formed.
  • a suitable fibrous matrix has been described in general terms in the sections hereinabove.
  • a fibrous matrix may be provided as one or more pre- formed, optionally pre- bonded web(s) supplied to the process before performing the meltfusion bonding.
  • such a fibrous matrix can be formed essentially in-line, i.e. in a continuous process with the forming of the unbonded structure loaded with SAP particles whilst or after the forming of the fibrous matrix and the meltfusion bonding thereof.
  • a formed fibrous matrix can exhibit an essentially homogeneous pore size distribution or may comprise z- and/or x-, y- directionally arranged distinct or gradually changing pore size distributions.
  • the fibrous matrix may also be provided by combining one or more of each of the above alternatives, such as by providing a pre-formed and pre- bonded web and accumulating in-line further fibres to form a composite fibrous matrix.
  • the means and the ways to create such fibrous matrix are generally not critical for the present invention and are well known in the art.
  • the fibrous matrix may be further modified during the process according to the present invention as will be discussed in more detail herein below.
  • the SAP particles may be provided by conventional means and may be metered continuously at a constant or predetermindly changing feed rate or intermittently, as well known in the art.
  • the meltfusionable material may be integral with the fibrous material.
  • the meltfusionable material may be provided separately, such as by adding meltfusionable material to the fibrous matrix.
  • the meltfusionable material may be in granular form added to the fibrous matrix analogously to the addition of the SAP particles or even mixed with the SAP particles.
  • the meltfusionable material is provided as one or more web materials as may be positioned on the surface of the absorbent structure or which may comprise fibres of the fibrous matrix on both sides of the web of the meltfusionable material.
  • the SAP particles may be added in a single step, or there may be several steps providing SAP particles at various stages of the process.
  • the particles are integrated into the fibrous structure.
  • the particles are supplied by gravity and/or a forced air flow to a pre- formed fibrous structure. Additionally or alternatively the particles can be supplied by gravity and/or a forced air flow whilst the fibrous matrix is formed.
  • the positioning of the SAP particles in the pores of the fibrous matrix may be aided by applying air flow, such as air suction z-directionally through the fibrous matrix.
  • such an air flow may be x-y-directionally homogeneous, or may be adapted to match x-y-directional pattern of the bonding regions and / or of substructures.
  • the positioning may be aided by applying other mechanical energy, such as tapping, shaking or the like.
  • the particles may be provided to the fibrous structure whilst or shortly after the pore size of the fibrous matrix has been modified as described herein below.
  • the relation of the pore size respectively interfibrous voids to the size of the SAP is such that in a dry state the SAP readily fits into and even can readily penetrate into the voids, but also such that the swollen SAP is restrained by the porous structure.
  • Fig. 2 It depicts schematically and not to scale the particle size distribution of particulate SAP, shown by the solid line curve 1100 of relative amount 1110 of particles (see left axis) exhibiting a certain diameter, see size 1000.
  • the area under the curve should sum up to 100%, and also that such a smooth curve 1100 is often determined by sieving into certain fractions.
  • both tails of the particle size distribution may be "cut off, such as for processing reasons, such that the particle size distribution shows a clear minimum (1010) and maximum (1020) value.
  • the diagram further shows - also schematically and not to scale - a pore size distribution of a fibrous matrix,
  • the dashed line 1200 shows for certain pore diameters or sizes 1000 the relative frequency 1210.
  • the area under the curve should sum up to 100%.
  • the tail may extend towards very small pores, here indicated by the cut off 1210 at the left axis.
  • the matrix exhibits a maximum pore size 1220. It should be noted that for the present explanation the term "pore size" refers to matrix of fibres only, i.e. there are no SAP particles considered.
  • SAP particles need to penetrate into the pores of the fibrous matrix. If there are sufficiently large pores, the particles may be embedded, if not, some of the particles will remain on the surface of the fibrous matrix. If a large particle is positioned on a pore region exhibiting too small pores for penetrating into, the particle may be moved into neighbouring larger pores, such as by tapping or air blowing or sucking or other embedding aids. If the particles are relatively too small, they might penetrate through the fibrous structure and - if present - be caught by an additional carrier. Also, even for an even pore size distribution smaller particles can be caught by relatively larger pores in analogy to the depth filtering mechanism.
  • the ability of the fibrous matrix to retain SAP particles will not only depend on the pore size distribution. For example, even if there is a small frequency of small pores, an increase of the thickness of the web, i.e. of the basis weight, will increase the ability of the structure to accommodate a given amount of small particles.
  • the dash-dotted line 1300 depicts the pore size distribution of a fibrous matrix exhibiting relatively small pores.
  • the pore size of such a fibrous matrix may be shifted to larger values, such as to a curve 1200, by submitting the fibrous matrix to process steps that temporarily or permanently change the pore size respectively the pore size distribution, such as by tentering (i.e. x- and / or y-directional stretching of the structure), or mechanical activation, such as by submitting the web to an incremental stretching between two flat, profiled or intermeshing profiled rolls, such as described in general terms in WO2007/107846.
  • tentering i.e. x- and / or y-directional stretching of the structure
  • mechanical activation such as by submitting the web to an incremental stretching between two flat, profiled or intermeshing profiled rolls, such as described in general terms in WO2007/107846.
  • the method described therein involves providing fibrous web materials and providing a pair of rolls to form a nip through which the absorbent fibrous web materials are processed, where the rolls are selected from processes consisting of ring rolling, SELF, micro-SELF and aperturing of rotary knife.
  • the absorbent fibrous web materials are deformed by processing through the rolls.
  • such a process may be modified by activating a single fibrous matrix, which may already been loaded with SAP particles, which may - due to insufficient amount of large enough pores - not have penetrated into the pores prior to activating. After releasing the modifying forces, the fibrous matrix may maintain the increased pore sizes, or at least some of the pores may return to smaller pores. If SAP particles were in such pores reducing their size again, these would be captured even more strongly in their position.
  • a further web material having a prescribed pore size may be positioned on the surface of the fibrous structure, thereby preventing particles to leave the fibrous structure.
  • Particularly suited materials for this may comprise meltblown webs.
  • the combining of the various steps of adding the SAP particles and applying air flow, mechanical aids, or vacuum influence the distribution of the particles in the fibrous matrix.
  • a vacuum is applied to a fibrous matrix, this may impact the pore size of the matrix.
  • the particle deposition and distribution may be influenced by the vacuum not only by the suction effect on the particles but also by the suction effect on the fibrous matrix.
  • discrete meltfusion bond points are formed, preferably of the shape and in pattern as described hereinabove.
  • the fibrous matrix optionally combined with a further web, is guided through a gap formed by a pair of anvils whilst or after the temperature is or has been raised by an energy source to the softening, often the melt temperature of the meltfusionable material of the fibrous matrix or of the further web.
  • the softened or molten compounds form the bonding points.
  • Energy sources may be alone or in combination:
  • a particularly preferred execution for the energy source is sonic, more preferably ultrasonic energy emitted by a "sonotrode”, optionally a rotating sonotrode, such as described in US20050034820 and commercially available such as from Herrmann Ultraschall GmbH, Germany.
  • one of the anvils is a flexible support structure for supporting the fibrous matrix which is considered as counteracting anvils cooperating with the sonotrode.
  • the principles of such a process are described in the above mentioned applications WO2012/042055 (C4S, Schmitz) and GB1216670 (C4S, Schmitz, unpublished), which are expressly incorporated herein by reference.
  • the sonotrode When the sonotrode contacts the fibrous matrix, it compresses the matrix into the space between the most upwardly positioned support points, at which the meltfusioning takes place.
  • the fibrous matrix is gently pressed between the upwardly (i.e. towards the sonotrode) positioned parts of the helical spring, where elliptical melt fusion bonding points are formed.
  • the fibrous matrix is only slightly and typically reversibly deformed, unless specific means are implemented such as additional support member between the helical springs that can provide a desired moderate compaction also outside of the bonding points.
  • the particular execution with the flexible anvils is believed to provide a further advantage in that it allows creating essentially particle free bonding regions even if the SAP particles are applied evenly across the x-y- direction.
  • the shape of the anvil structure exhibiting essentially no flat surface but rather a surface sloping away in all directions allows the SAP particles located in the bonding regions to dislocate slightly just prior to the bonding outside of the bonding regions.
  • the forming of the meltfusion bond region is creating regions of varying densities around the bonding regions. Whilst no strong compression between the heat source, such as the sonotrode and the anvil elements is deemed to be necessary, the melting of the meltfusionable material will inevitably increase the local density of the materials in the bonding region, and - as the local basis weight per unit area remains essentially constant - reduce the calliper of the structure in the bonding points.
  • Fig. 3A depicts a SAP particle supply 500, such as conventional hopper with a dosing unit (not shown).
  • Particulate SAP falls in a stream 510 onto a fibrous matrix, here shown as a pre-bonded web, as may be a high-loft material described herein above, that is supported by a support structure, here shown as helical anvil system on a rotating drum 720.
  • the fibrous matrix with the SAP particles are fed towards a gap between the anvil and a heat source, here shown as rotating sonotrode 800 of a ultrasonic welding system to form the meltfusion bonded absorbent structure 999.
  • Fig. 3B depicts a similar system, wherein the fibrous structure loaded with SAP particles is fed into a gap between two interdigitizing mechanical activation rolls 900 and 910 for modifying the pore size distribution of the fibrous structure. Thereafter, the fibrous matrix is bonded as described in the context of Fig. 3A to form the absorbent structure 999.
  • Fig. 3C depicts a similar system as shown in Fig. 3B, now with additional web materials, such as carrier web 620 and a cover web 630 enveloping the fibrous matrix before all three are meltfusion bonded to form the absorbent structure 999.
  • Fig. 3C depicts a further combination of process elements, here showing two SAP particles supply systems, which may provide essentially the same or different types SAP particles,
  • a first stream of particles 510 is fed as shown in Fig. 3B to the fibrous web 600 just prior to the mechanical activation between interdigitizing rolls 900 and 910, whilst a second stream of particles 515 is fed towards rotating drum 720 with the support structure, here a helical anvil 700 prior to bonding with sonotrode 800 to form the absorbent structure 999.
  • the particle stream 510 may be modulated so as to provide a varying distribution of particles upon lay down.
  • This modulation may be by any means resulting in a variation across the y-direction and/or the x-direction.
  • the latter may be achieved by interrupting the particle stream, such as by blowing or sucking air and thus removing the particles from the stream for a predetermined time.
  • a very convenient and simple construction employs a vacuum cylinder rotating around its axis which is positioned between the SAP metering device and the rotating drum 720 in the proximity of the particle stream and oriented along the y-direction.
  • the cylinder further comprises a slit of a predetermined width, such that when the slit is oriented towards the particle stream, the particles are sucked into the cylinder, from where they may be recycled to the SAP particle supply system, but alternatively they may be fed towards the rotating drum on which already a carrier material is positioned, such that in such a predetermined region an increase of SAP basis weight can be realized.
  • a comparative example has been constructed according to the teaching of co-pending application GB1216670.
  • topsheet a 19 g/m 2 hydrophilic spunbonded polypropylene nonwoven material
  • a set of intermeshed helical springs having a circular wire diameter of 1.5 mm, an outer spring diameter of 1 cm and a pitch of 1.7 cm, covering an area of about 20 cm 20 cm.
  • a cardboard mask with a square opening of 10 cm by 10 cm was placed thereon and slight vacuum was applied from underneath the support board for the set of helical springs to ease flat positioning of the topsheet layer and create slight indentations or pockets between the uppermost support points.
  • a second topsheet layer of 20 cm by 20 cm was positioned over the first and the SAP particles, thusly forming a sandwich structure.
  • a second ultrasonic bond line was made circumferentially outwardly of the sandwich region, forming a 15 cm by 15 cm square.
  • a second sample was constructed according to the teaching of the present invention.
  • One layer of conventional topsheet a 19 g/m 2 hydrophilic spunbonded polypropylene nonwoven material, has been cut to about 20 cm by 20 cm and placed on a set of intermeshed parallel helical springs, having a circular wire diameter of 1 mm, an outer spring diameter of 1.5 cm and a pitch of 1.7 cm, covering an area of about 20 cm 20 cm.
  • a cardboard mask with a square opening of 10 cm by 10 cm was placed thereon and slight vacuum was applied from underneath the support board for the set of helical springs to ease flat positioning of the topsheet layer.
  • a second topsheet layer 20 cm by 20 cm was positioned over the surface of the high-loft material.
  • the three webs were meltfusion bonded at the uppermost support points of the helical springs, thereby creating elliptical bonding points of approximately 1.5 mm length and about 0.5 mm width.
  • a second ultrasonic bond line was made circumferentially outwardly of the sandwich region, forming a 15 cm by 15 cm square. Both samples were evaluated by being loaded with 0.9% saline solution.
  • the samples were placed in a dish of 40 by 40 cm with the first topsheet side down. 120 ml of 0.9 % saline solution were added to the dish and the swelling of the structures was observed.
  • the structure expanded z- directionally, thereby pulling the outward second ultrasonic bond line inwardly without de-bonding it.
  • the comparative sample did not exhibit any structural integrity, i.e. the nonwoven webs did not retain any of the swollen particles.
  • the inventive sample could be lifted from the dish essentially without losing any of the swollen particles.
  • the measurements should, unless stated otherwise, be carried out at an ambient temperature of 23 ⁇ 2° C. and a relative atmospheric humidity of 50 ⁇ 10%.
  • the water- absorbent polymers are mixed thoroughly before the measurement.
  • the saline flow conductivity is, as described in EP 0 640 330 Al, determined as the gel layer permeability of a swollen gel layer of water-absorbent polymer particles, although the apparatus described on page 19 and in FIG. 8 in the aforementioned patent application was modified to the effect that the glass frit (40) is no longer used, the plunger (39) consists of the same polymer material as the cylinder (37) and now comprises 21 bores having a diameter of 9.65 mm each distributed uniformly over the entire contact surface. The procedure and the evaluation of the measurement remains unchanged from EP 0 640 330 Al , except for using 0.9 % saline solution instead of Jayco Synthetic Urine. The flow rate is recorded automatically.
  • SFC saline flow conductivity
  • L0 is the thickness of the gel layer in cm
  • d is the density of the NaCl solution in g/cm 3
  • A is the surface area of the gel layer in cm 2
  • WP is the hydrostatic pressure over the gel layer in dyn/cm 2 .
  • centrifuge retention capacity of the water-absorbent polymer particles is determined by the ED ANA recommended test method No. WSP 241.2-05 "Centrifuge Retention Capacity", wherein for higher values of the centrifuge retention capacity lager tea bags have to be used.
  • the absorbency under high load of the water-absorbent polymer particles is determined analogously to the EDANA recommended test method No. WSP 242.2-05 "Absorption Under Pressure", except using a weight of 49.2 g/cm 2 instead of a weight of 21.0 g/cm 2 .
  • the EDANA test methods are obtainable, for example, from the EDANA,-Avenue Herrmann Debroux, 46; B-1 160 Brussels, Belgium.

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  • General Health & Medical Sciences (AREA)
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  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • Public Health (AREA)
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  • Biomedical Technology (AREA)
  • Manufacturing & Machinery (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Fluid Mechanics (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Nonwoven Fabrics (AREA)
  • Laminated Bodies (AREA)

Abstract

La présente invention concerne une structure absorbante comprenant une matrice fibreuse (110), un matériau pouvant être fusionné à chaud et des particules polymères superabsorbantes (140). La structure absorbante est collée par un motif de point de collage par fusion à chaud (200), qui est de préférence créé par soudage ultrasonore.
PCT/EP2013/063595 2012-06-29 2013-06-28 Structure absorbante collée par fusion à chaud comprenant des fibres et des particules superabsorbantes et procédé de fabrication d'une telle structure WO2014001487A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP13734372.9A EP2872096B1 (fr) 2012-06-29 2013-06-28 Structure absorbante collée par fusion à chaud comprenant des fibres et des particules superabsorbantes et procédé de fabrication d'une telle structure
CN201380043750.0A CN104602658B (zh) 2012-06-29 2013-06-28 包含纤维和超级吸收剂颗粒的熔融结合的吸收剂结构及用于制造这种结构的方法
US14/411,889 US10239284B2 (en) 2012-06-29 2013-06-28 Meltfusion bonded absorbant structure comprising fibres and superabsorbant particles method for manufacturing such structure

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
GB201211577A GB201211577D0 (en) 2012-06-29 2012-06-29 Method and apparatus for the manufacturing of sandwich structures with free flowing materials and such structures
GB1211577.0 2012-06-29
GB1216670.8A GB2504783A (en) 2012-06-29 2012-09-19 Sandwich structure containing free flowing material
GB1216670.8 2012-09-19
GB1220625.6A GB2503529A (en) 2012-06-29 2012-11-16 Meltfusion bonded absorbent structure comprising fibres and superabsorbent particles
GB1220625.6 2012-11-16

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016166368A1 (fr) * 2015-04-17 2016-10-20 Concepts For Success (C4S) Équipement et procédé permettant de créer des régions dépourvues de particules dans un voile fibreux chargé de particules
WO2018184051A1 (fr) 2017-04-03 2018-10-11 Lenzing Ag Matériau non tissé conçu pour être utilisé dans des structures de cœurs absorbants ayant des capacités d'acquisition/distribution intrinsèques
WO2019158672A1 (fr) 2018-02-15 2019-08-22 John Blevins Élément absorbant pour un produit adapté à une fente corporelle et produit comportant un tel élément absorbant
WO2023070240A1 (fr) * 2021-10-25 2023-05-04 Kimberly-Clark Worldwide, Inc. Noyaux absorbants et leurs procédés de fabrication
EP4331546A1 (fr) 2022-08-31 2024-03-06 HyPro Innovation GmbH Tampon absorbant à effet thermique
EP4450033A1 (fr) 2023-04-20 2024-10-23 Fabio Zampollo Toile composite absorbante comprenant une couche à haute porosité et des particules entremêlés avec des micro-filaments continus

Families Citing this family (2)

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IT201700031281A1 (it) * 2017-03-22 2018-09-22 Gdm Spa Apparato e metodo di formatura di una imbottitura assorbente.
CN116348079A (zh) * 2020-10-30 2023-06-27 宝洁公司 包含共成形层的吸收性结构

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JPH06190001A (ja) * 1992-12-24 1994-07-12 Sekisui Plastics Co Ltd 吸水シートおよびその製造方法
US20010006089A1 (en) * 1999-12-22 2001-07-05 Kenji Ando Method for manufacturing particle deposited body
JP2002159533A (ja) * 2000-11-27 2002-06-04 Kao Corp 吸収性物品
WO2012042055A1 (fr) * 2010-10-01 2012-04-05 Concepts For Success (C4S) Formation de régions de consolidation dans une bande et bande comprenant de telles régions

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FR2617020B1 (fr) * 1987-06-26 1993-09-24 Boussac Saint Freres Bsf Matelas absorbant perfectionne, notamment pour des produits d'hygiene, et procede de fabrication en continu de tels matelas
DE102009055951A1 (de) * 2009-11-27 2011-06-01 Glatfelter Falkenhagen Gmbh Absorbierende Struktur

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JPH06190001A (ja) * 1992-12-24 1994-07-12 Sekisui Plastics Co Ltd 吸水シートおよびその製造方法
US20010006089A1 (en) * 1999-12-22 2001-07-05 Kenji Ando Method for manufacturing particle deposited body
JP2002159533A (ja) * 2000-11-27 2002-06-04 Kao Corp 吸収性物品
WO2012042055A1 (fr) * 2010-10-01 2012-04-05 Concepts For Success (C4S) Formation de régions de consolidation dans une bande et bande comprenant de telles régions

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016166368A1 (fr) * 2015-04-17 2016-10-20 Concepts For Success (C4S) Équipement et procédé permettant de créer des régions dépourvues de particules dans un voile fibreux chargé de particules
WO2018184051A1 (fr) 2017-04-03 2018-10-11 Lenzing Ag Matériau non tissé conçu pour être utilisé dans des structures de cœurs absorbants ayant des capacités d'acquisition/distribution intrinsèques
WO2019158672A1 (fr) 2018-02-15 2019-08-22 John Blevins Élément absorbant pour un produit adapté à une fente corporelle et produit comportant un tel élément absorbant
WO2023070240A1 (fr) * 2021-10-25 2023-05-04 Kimberly-Clark Worldwide, Inc. Noyaux absorbants et leurs procédés de fabrication
GB2626701A (en) * 2021-10-25 2024-07-31 Kimberly Clark Co Absorbent cores and methods of manufacturing
EP4331546A1 (fr) 2022-08-31 2024-03-06 HyPro Innovation GmbH Tampon absorbant à effet thermique
WO2024046733A1 (fr) 2022-08-31 2024-03-07 Hypro Innovation Gmbh Serviette absorbante à effet thermique
EP4450033A1 (fr) 2023-04-20 2024-10-23 Fabio Zampollo Toile composite absorbante comprenant une couche à haute porosité et des particules entremêlés avec des micro-filaments continus

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