CA1308241C - Nonwoven materials - Google Patents

Nonwoven materials

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Publication number
CA1308241C
CA1308241C CA 572536 CA572536A CA1308241C CA 1308241 C CA1308241 C CA 1308241C CA 572536 CA572536 CA 572536 CA 572536 A CA572536 A CA 572536A CA 1308241 C CA1308241 C CA 1308241C
Authority
CA
Canada
Prior art keywords
nonwoven
fibres
loftable
lofted
particle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA 572536
Other languages
French (fr)
Inventor
Michael J. Seal
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bonar Carelle Ltd
Original Assignee
Bonar Carelle Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bonar Carelle Ltd filed Critical Bonar Carelle Ltd
Application granted granted Critical
Publication of CA1308241C publication Critical patent/CA1308241C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4326Condensation or reaction polymers
    • D04H1/435Polyesters
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/60Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in dry state, e.g. thermo-activatable agents in solid or molten state, and heat being applied subsequently
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495Thickness [relative or absolute]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982Particulate matter [e.g., sphere, flake, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/699Including particulate material other than strand or fiber material

Abstract

NONWOVEN MATERIALS
ABSTRACT
A nonwoven material comprises a lofted or loftable, particle bonded nonwoven having fibres bonded together with an adhesive binder and containing functional particles (e.g. particles of a liquid-absorbent polymer) distributed therein and attached to the fibres by the adhesive binder.

Description

13~8~:41 NONWOVEN MATERIALS
-Field of the Invent~on The present invention relates to nonwoven materials that compri~e a lofted or loftable, fibrous matrix and functional particles, e.g. particles of a superabsorbent polymer, held wlthin the matrix.
Back~round to the Invention Conventionally, cellulose wadding or fluff pulp is employed as the primary absorbent material in absorbent products such as babies' disposable ~apkins, incontinence pads for adult use and catamenials~ However, although such cellulose absorbents are inexpensive, their absorbency is not especially high.
In recent years, polymers have been developed that have a very high absorbency with respect to aqueous liquids. Thus, hydrophilic polymers have been developed that can absorb more than 15 parts by weight of water per part of polymer. It ran be readily envisaged that the partial or complete substitution of these so-called superabsorbent polymers for the cellulose absorbents that have been widely used hitherto might offer significant advantages by permitting the production of absorbent products that have increased absorber.cy and/or lower bulk. However, it has proved difficult to incorporate superabsorbent polymers into absorbent products in a satisfactory manner. ~
One problem with such supera~sorbent polymers is that they should be prevented from coming into contact with the skin of the user of the absorbent~product. Two techniques for overcoming that problem have been proposed in the art. The first technique lnvolv~s the coating of one surface of a layer within the absorbent product with a hot-mel~ adhesive and bonding the particles of superabsorbent polymer into the product by means of that adhesive. The second technique is to confine the ~: .

13~824~

superabsorbent polymer particles by means of tissue paper.
However, both of these techniques have the disadvantages that they involve additional expen~e (due to the cost of the extra material, namely the hot-melt adhesive or the tissue paper, as the case may be) and that the efficiency of the superabsorbents i8 impaired. Thus, whereas the hot melt adhesive will block part of the urface area of the superabsorbent particles in the first of these prior-art proposals, the tissue paper used in the second of the proposals may provide the superabsorbent particles with insufficient space for swelling as they absorb moisture.
The prior-art proposals for incorporating superabsorbeDt polymers into absorbent products have generally involved the use of laminated structures. It is suggested in EP-A-0,202,472 that often the resulting products are easily delaminated with impaired absorbency.
That European Patent Specification discloses a non-laminar absorbent product comprising matrix fibres (specifically cellulosic fibres or a mixture of cellulosic fibres and synthetic staple fibres) having a liquid-absorbing material (such as a superabsorbent polymer) bound within the matrix fibres by means of a heat-activated binder material. The binder may be thermoplastic or thermosetting and may, for example, be incorporated into the matrix in the form of a powder. In the exemplary embodiments of the process for producing~the non-laminar absorbent product, matrix fibres are laid down iD a first layer, a superabsorbent powder is~evenly distributed thereover and a second layer of matrix fibres is laid down over that. Thus, in the continuous process illustrated therein, a mat is formed by laying down the matrix fibres on a web-forming device at two locations, a llquld-absorbing material being dlstributed amongst the ' .

~ ` 1308Z~

~atrix fibre~ at a location intermediate the said locations at which the matrix fibres are laid down. Such an arrangement i8 ~aid to ensure that the ab30rbent is not exposed on one surface of the finished absorbent web ~EP-A-0,202,472 at page 12, line~ 18-27).
Summary of the Invention The present invention provides a nonwoven ~aterial that compri~es a lofted or loftable, particle-bonded nonwoven, said nonwoven having ~ matrix of fibre~ that are bonded together with an adhesiYe binder, functional paxticles being di~tributed within the matrix and attached to the said fibres by means of the ~aid adhesive blnder.
The present invention also provides ~ process for producing a nonwoven material, wherein functional particles are distributed within a matrix of fibres containing an adhesive binder, said matrix forming a lofted particle-bonded nonwoven, and at least some of the functional particles contac~ the adhesive binder while the latter is in a molten or softened state. Preferably, the functional particles are applied to a loftable, particle-bondad nonwoven, and the nonwoven is thereafter subjected to heat so that it undergoes lofting. The re ultant lofted nonwoven may then, for example, be either eooled in its lofted state or subjected to sufficient pressure to compact it into a denser, loftable material.
Brief_description of the drawin~s Figure 1 is a flow-sheet showing various stages in the manufacture of an absorbent nonwoven material according to this invention.
~ Figure 2 is a photomicrograph of a section through an absorbent nonwoven material according to this invention.
Figure 3 is a photomicrograph of a section through an absorbent nonwoven material according to this invention at a higher magnification than that of Figure 2.
Description of preferred embodiments The fibres in the nonwoven material may be selected, for example, fro~ natural f~bres (e.g. cotton linters), D8; ~

regenerated fibres (e.g. viscose rayon) and synthetic polymers (e.g. polyesters, such as poly(ethylene terephthalate), polyamides such as nylon 6 or nylon 6, 6, and polyalkylenes such as polypropylene), as well~as any mixtures of two or more such fibres. At present polyester fibres are preferred.
The fibres will have a staple length usually of from 25 to 100 mm, preferably from 35 to 60 mm, and a linear density usually of from 0.5 to 20 dtex, p~eferably from 1.5 to 15 dtex. Suitable fibre diameters will usually be from 1 to 50 ~m, preferably 5 to 40 ~m and typically 10 to 3~
um. However, the stated ranges for the aforesaid physical parameters should not be seen as limitative; the skilled person may select the fibre characteristics as appropriate for any given application.
The loftable nonwoven will usually have a basis weight of from 30 to 120 g/m2, preferably from 50 to 95 g/m2. The thickness of the loftable nonwoven will be typically from 0.25 to 1 mm.
The nonwoven material may be made using particles of bonding material of any suitable size and shape, for example the rods or granules disclosed, respectively, in US
patents No. 2,880,112 and No. 2,880,113 to A.H. Drelich.
It is, however, preferred to employ nonwoven material pro-duced using recent powder-bonding technology (see, for example, M.F. Meyer, R.L. McConnell and W.A. Haile, "Production of laminates and nonwovens by powder bonding", a paper presented at the INSIGHT '85 Advanced Forming/Bonding Conference, 27-29th October, 1~85, Toronto, Canada). In a typical powder-bonding process, a layer of ~ibres is formed, preferably by dry-laying, a particulate bonding mat~rial is applied to the resultant layer and distributed therethrough, the resultant fibrous web is passed through a heating zone in which the particles are softened or melted, and the web is then passed through a zone in which it is compressed in order :~
'~

~3Q8241 to lncrease the contact of the molten or softened bonding material with the fibre~, after which the resultant material i8 cooled in order to solidify the bonding material and thereby to bond the fibres at points throughout the fibrou6 matrix.
The bonding powd r should have a lower melting p~int than the fibres in the web; the bonding powder will commonly be of a ma*erial having a melting point in the range 80 to 180C. In general, the bonding powder will be a thermoplastic material and it should be capable of forming a good adhe~ive bond with the fibres being used.
In a number of cases, especially in the case of polyester fibres, a polyester bonding powder will be found to be suitabl~, for example the polyester powders available from Eas~man Chemical Products Inc~ as hot-melt adhe~ives under the trade mark ~Eastobond~. Typical polyester adhesives have melting points of from 110 to 130 C and are available as coarse powderæ (200 to 420~m or 70-40 US standard mesh), medium powders (80 to 200 pm or 200-70 US standard mesh) and fine powders (80pm or less or finer than 200 US
standard mesh), the medium powders being preferred when the powder is to be added to the fibrous web using a mechanical applicator.
Other adhesive binders, for example epoxy resins, also come into consideration.
The amount of powder deposited in the web would usually be from 5 to 50% of the total fabric weight, preferably from 10 to 20%.
The required lofting capability may be achieved by the use of fibres that are crimped; cuitable fibres include the crimped polyester fibres, for example such fibres-having hollow cross-sections, that are marketed by Eastman Chemical Products Inc. for fibrefill applications. The lofting mechanism may be explained as follows. As laid, the fibrous web will be thick and of low density owing to the highly crimped form of the fibres that are used. When this web is trea~ed with the bonding powder and then .

f . ~ 8~

compre~sed (e.g. calendered~ in the fabr~c-making process, the adhesive powder bonds hold down the fibres and constraln them in a flat sheet form. ~t i8 in thi6 (~den~lfied" or ~compressed~) form that the fabrlc i8 removed from the fabric-making line. The lofting process occurs when the adhesive powder bonds are softe~ed by heat. The adhe~ive bonding material melts at a temperature (typically 110 to 130 C) that i8 much lower than the melting temperature of the fibres ~typic~lly 250 to 290C). When heated, therefor~, the powder bonds coften and allow the fibres to ~regai~ their memorya and thereby tend to return to the thick, low density form that they were in prior to adhesive bonding. Typically, the lofting temperature will be in the range of 120 to 220 C.
The lofted material then cools in its lofted state and the adhesive resets and thereby stabilises the web i~ its lofted for~.
Normally, the loftable material would be capable of an increase in thickness of typically 5 to 10 times the original thickness upon heating.
Suitable loftable powder-bonded nonwovens are marketed by Bonar ~arelle Limited under the trade name ~Carelle Ultraloft" in various grades, e.g. P50, with a basis weight of 50 g/m2 and an unlofted thickness of 0.31 mm, and P95 with a basis weight of 95 g/m2 and an unlofted thickness of 0.61 mm. (Basis weights were measured by the EDANA 40-2-77 test method and thickness by the EDANA
30-3-78 test method.) The expression "functional particles~ includes, for example, functional powders and functional granules. The invention is not limited with regard to the particle shapes, although spherical and substantially spherical particles are at present preferred.
In certain preferred embodime~ts, the functional particles comprise or consist of hydrophilic polymers having the ability to absorb aqueous liquids, especially the so-called super-absorbent polyers. Numerous ~t~ R~
,~

3L3Q~32~

hydroph~lic polymers are known, these mainly f~lling lnto three classes, namely the starch graft copolymer3, the cro~s-linked carboxymethyl cellulos~ derivatives and the modified polyacrylates, particular 3ub-classes being carboxylated cellulo~e, hydrolyzed acrylonitrile-grafted starch, acrylic acid derivative polymers, polyacrylonitrile derivatives, polyacrylamides and saponified vinyl acetate/methyl acrylate copolymers.Commercially available superabsorbents include the polymers available und~r the trade mark ~Water Lock~
~Grain Processing Corporation, USA), and which are described in US-A-3,661,815 and, amongst the acrylic acid and methacrylic acid polymers and copolymers, which are preferred herein, ~uperabsorbent polymers are available under the trade marks ~Sanwet~ (Sanyo Kasei Kogyo R.K., Japan), ~Sumika Gei~ (Sumitomo Ragaku K.K., Japan) and nAqua KeepN (Norsolor, France). The particles of hydrophilic polymer, before absorption of water, preferably have a weight-average particle size of frsm 75 to 800pm, more preferably from 100 to 500pm.
Research by the present Applicant suggests that it is possible to add up to 300% of superabsorbent relative to the weight of the nonwoven (e.g., up to 150 g/m2 superabsorbent within a nonwoven having a basis weight of 50 g/m2). However, at such high levels, there may be a deterioration in the absorption efficiency and it is preferred to utilise addition levels of from 20 to 100% by weight of the nonwoven.
It will be understood, however, that the present invention is not limited to the use of functional particles that are liquid-absorbing polymers. Other functional agents in particulate form that could be used include, for example, activated charcoal (e.g. for absorbing odours and/or absorbing micro~organisms), medicaments, including antibacterial or antimycotic agents ~3~82~.

(for instance, in appllcations where slow release of the medicament is required); and metallised microspheres (for rendering the nonwoven X-ray detectable).
The loftable nonwoven may be constituted by the loftable phase of a two-phase nonwoven, the other phase being non-loftable, as disclosed in copending European Patent Specification No. 0,269,380 A2. Such two-phase materials are advantageous, in that they eliminate the need for the coverstock conventionally used in such absorbent products as diapers and the like, since the non-loftabl-e phase provides an acceptable surface for presentation to the skin of the user. As described in European Patent Specification No. 0,269,380 A2 an absorbent layer is sandwiched between the two-phase nonwoven (adjacent to the loftable phase of the latter) and an impermeable backing sheet, the said loftable phase acting as a "dry bridge" to inhibit re-wetting of the surface by the absorbed liquid.
However, the present invention offers the possibility of dispensing with the discrete absorbent layer, since a liquid-absorbing particulate material may now be incorporated within the loftable or lofted phase itself.
The distribution of the liquid-absorbing (or, indeed, other functional) particles within the lofted phase may be uniform or even (or substantially so) or it may be differential with, for example, the concentration of the particles being at its lowest (e.g. substantially zero concentration) at the interface with the non-loftable layer, increasing to the greatest value adjacent the surface remote from the non-loftable phase. Usually, the non-loftable phase will be kept free or substantially free of the liquid-absorbing (or other functional) particulate material; this is due to the much more closed nature of the structure in this phase.
Usually, the non-loftable phase will have a basis weight (or "grammage") of from 10 to 50 g/m2, preferably ;~ ~

l.~ Z~

15 to 25 g/m2. The loft~ble phase (i.e. in lt~ densified form) may h~ve ~ ba~i~ wei~ht in ~he broad range, 30 to 120 g/m2, indicated above; however, typic~lly the loftable phase wlll have a ba~is weight of from 30 to 89 g/m2, preferably from 50 to 60 g/m2~ The thicknes~ of the non-loftable phase will b~ typically from 0.03 to 0.25mm, whereas the thickne~s of the loftable phase (in its densified form) will be typically from 0.25 to lmm.
As indicated in European Patent Specification No.
0,269,380 A2, it 18 also possible to construct a multi-phase nonwoven ma~erial having three or more phases, at least one of which iB a lofted or loftable phase.
By way of illustration, the production of a nonwoven material according to the present invention i~ described below with reference to the productlon line shown schematically in Figure 1.
This pxoduction line comprise~ an open-mesh conveyor belt 20 which is driven around the rollers 22, 24 in the direction indicated by the arrow A. One or more textile cards- represented by the single device 26 - are provided in order to deposit a layer 28 of fibres on the upper flight of the conveyor belt 20. The layer 28 constitut~s a precursor of the loftable nonwoven.
If a two-phase nonwoven is required, another layer 30 of fibres is deposited on top of the layer 28 from one or more further textile cards, represented by the single device 32. In such cases, the layer 28 may constitute the precursor of either the loftable or the non-loftable phase of the nonwoven, the layer 30 constituting the precursor of the other phase. With this method of manufacture, there will be a measure of interpenetration of fibres from the two phases at the junction thereo~, this being regard~d as an asset in that it helps to preserve the integrity of the nonwoven sheet material during shipping, conversion into the end product and use.
A single-layer or two-layex web, now identified by the reference numeral 34, i8 passed through a web-spreading Z~l section 36 and then to a zone in whlch the powdered bonding material i8 applied to the web. Thi~ zone ~8 represented by the powder-depositing device 38 (although in prac~ice a plurallty of such devlces may be used).
Suitable powder-depositing device~ ar~ powder applicators of the known type in whlch a wired roller takes powder i~to the space between the wire~ and, upon rotation, drop~
the powder out of ~hat space onto the fibrous web pa~sing beneath it. A screw 40 may be provided ln order to raise or lower the roller of the powder-depo~iting device 38.
Furthermor~, a receptacle 42 is provided in order to catch any excess powder that falls through the open-mesh belt 20, the powder so collected being available for recycling.
It will be appreciated, of course, that as an alternative to mechanical powder-depositing devices, other applicators such as a fluidising air spray or an ~lectrostatic spray-gun com~ into consideration, as do devices that apply the powder in a liquid carrier or in the form of a foam.
The web 34, now with bonding powder distributed through it, is transferred from the conveyor belt 20 to a further conveyor belt 44, for example of Teflo~ coated fibreglass, which belt 44 is driven round rollers 46, 48 in the direction indicated by the arrow B and serves to carry the fibrous web 34 through an infrared oven 50.
Within the oven 50, ~he bonding powder fuses and bonds the fibres of the web at points where the fibres and the bonding material come into contact. Upon leaving the oven 50, the web 34 is subjected to light pressure by means of the nip roll 52~
It has been found that the strength of the web material can be improved by reheating. Accordingly, the web 34 le~ving the nip roll 52 is tran~ferred to another conveyor belt 54 which i~ driven round roller~ 56, 58 in the direction indicated by the arrow C. Ac it contacts the conveyor belt 54, the web 34 is carried beneath a wa~er-cooled lightweight roller 60. The web is then ~3~82~

carried through a second oven 62 and thereaft~r i~
subjected to further compr~ssion by means of the nip roll 64. The nip rolls 52 and 64 may be heated during start up but thereafter cooled during operation. The rollexs 46, 48 and 56, 58 may al~o be wat¢r-cooled in order to pravent an excessive build-up of temperature due to the tran~fer of heat from the ovens. The resultant we~ ls then further cooled by passlng it around the water-cooled can~ 66, 68, following which the web is wound into roll 70 on a suitable winder.
The ~uitable oven temperatures will depend upon the bonding powder that is used and will be ascertainable from simple trials or from the literature provided by the supplier of the bonding powder. Typically, however, the oven temperatures will be within the range fr~m 80 to 200 C. The temperature of the web emerging from the ovens 50 and 6~ may be monitored, for example by mean~ of infrared devices 72 and 74, r~spectively~ It will be appreciated, of course, that the infrared ovens 50, 62 could be replaced by other heating devices, e.g.
calenders, hot-air ovens; steam pr~sses and heated contact cans with non-stick surfaces. The dwell time of the web in each oven will depend upon the line speed that is achievable (typically from 50 to 100 metres per minute, although higher speeds may be possible) and other factors, but may typically be from 20 seconds to 2 minutes, The pressures applied by the nip rolls 52 and 64 will depend upon the materials us~d, the desired characteristics of the web and the process line conditions; normally, pressures of up to 30 kg, typically up to 20 kg, per cm of roll face width are used.
Clearly, a given volume ean con~ain a greater weight of unlofted material than lofted material and it is therefore preferred, for reasons of economy, to transport and store the sheet material in the unlofted state prior to further processing.
AB required, densified web 34 (or a two-phase web containing a densified, loftable phase) is fed on to a - ~3L36~8Z~

conveyor which is represented by (but not necessarily limited to) a conveyor belt 72 which is driven round rollers 74, 76 in the direction indicated by the arrow D.
The web 34 may be fed from a roll 70 of the material;
alternatively, it could, in principl~, be obtained directly from the water-cooled cans 66,68. The conveyor 72 serves to carry the fibrous web 34 through a zone in which functional particles may be applied to the web from an applicator device 78. In the case of a two-phase web it is preferred to apply the particles to ~he loftable phase. The particulate material may be supplied from a fluidized bed powder hopper by means of a.venturi-effect powder pump to a spray gun of the electrostati~ type or compressed-air type (e.g. the Flexi-Spray (trade mark) powder gun manufactured by Nordson Corporation, Ohio, U.S.A). Other equipment suitable for the application of particles of liquid-absorbent polymer utilizes a dosing roller and is available from Santex AG, Tobel, Switzerland.
By adding the functional particles at this stage, rather than earlier in the process, the possibility of interference with the fibre-to-fibre bonding is largely avoided; moreover, the functional particles are Dot subjected to the earlier heating and high-pressure - .
calendering stages, which might have damaged them.
Usually, it is preferred to achieve a uniform or substantially uniform distribution of particles through the web. However, it is possible to achieve a differential distribution, for example by use of a vibratoxy system and/or by means of an appropriate seleotion of fibre characteristics and particle sizes of the functional particles.
The dense web to which the functional particles have been applied is then passed thrsugh an oven ~0 which is maintained at a tempera~ure at which lofting of the lo~table web (or phase) will occur. As the lofting ~3082~1 process is activated, the function~l particles tuDble into the opening fibrous structure. Only those particlss attaching to the molten or softened adhesive are retained. The lofted web emerging from the oven 80 (which may be, for example, of any of the types mentioned above as being suitable for the oven 50 or 62) comprises a matxix of fibres with the functional particles distributed through the matrix and attached to the fibres by means of the adhesive. The particles are retained predominantly in the spaces within the low density open structure.
A collection device 82 may be provided immediately after the conveyor 72 in order to collect unbonded particles that have dropped throuyh or spilled over the web. The lofted matexial emerging from the oven 80 could, after cooling, be used as such for conversion into the desired end product, for example a disposable diaper.
However, the nonwoven has normally to be transported to the converter and, in order to reduce transport costs, th~
web will ordinarily be fed to a calander 84, or a similar device, in order to re-densify it, the resultant dense material then being wound into a roll 86 on a suitable winder. The re-densified nonwoven may be lofted again, when required, by the application of heat tas described above).
The manner in which the functional particles may be distributed and fixed within a lof~ed nonwoven is shown in Figures 2 and 3, which are photomicrographs, at magnification x33 and x84 respectively, of an Ultraloft polyester nonwoven bonded with an Eastobond~polyester binder and having distributed therein particles of a superabsorbent polymer.
The matrix of fibres, especially in the lofted (or "bul~ed" or uncompressed") state, allows ample volume within which the superabsorbent polymers may expand when absorbing a liquid. Furthermore, the superabsorbent ~ ~ 3~32~

particles are attached to the blnder over a comp~ratively small proportion of their total surface area. Th~e factors, together with the good distrlbution of the particles through the fibrous matrlx, enable the superabsorbent polymer to ab~orb liquid ~n a highly ~flcient manner. Moreover, ~i~ce the nonwoven is an integrated struc~ure, ~here is little or no tendency to undergo delamination and, once the unbonded and ~v~rspill particles have been removed, the remaining particles are in general sufficiently well bonded to avoid ~ubQtantially the migration of loose particle~ within th~ nonwov~n and the loss of loose particles from the nonwoven~ The low incidence of large clusters or localised heavy concentrations of particles contributes to the efficiency of the absorption, since the phenomena such a~
gel-blocking (whereby, for instance, particles interfere with the absorption capability of other particles) are largely avoided.
The absorbent nonwoven material may be converted by conventional means into the desired end product, such as a --disposable absorbent product of the class that may be broadly described as "diapers", for example babies' napkins, incontinence pads for adult use and catamenial products. Commonly, the conversion will involve the attaching of the nonwoven material to a liquid-impermeable backing sheet, for example by meanQ of stitching or the use of an adhesive material. The absorbent product may be constructed in a co~ventional manner, using a coverstock layer; however~ it is preferred to employ a two-(or other multi-) phase nonwoYen, as described above. Other components, e.gl fastening tapes or the like, may be attached if required.
It will be appreciated, of course, that the absorben.
products of the present invention could be used outside the field ~f disposable personal hygiene aids~ For ~3Q824~L

instance, the products may be used in th~ medic~l field, a~ bandaqin~ or as wound dressings ~ubject tv approval by the appropriate regulatory body), or as wipes.
Further po~ible end uses for nonwoven materi~l~
according to ~his invention may be in durable or semi-durable good~, for instance neutralising agents ln flltra~ion, barrler agents in ~creening applications (eg.
~urveillance or interference), lnsulation, and in the constructioQ of protective layer~ around sensitlve equipment within envlronmentally controlled areas.
It wlll of courBe be under~tood that the present invention ha~ been de~cribed above purely by way of example, and modification of detail can be made within the scope of the invention.

Claims (19)

1. A nonwoven material that comprises a lofted or loftable, particle-bonded nonwoven, said nonwoven having a matrix of fibres that are bonded together with an adhesive binder, functional particles being distributed within the matrix and attached to the said fibres by means of the said adhesive binder.
2. A material according to claim 1, wherein the said matrix comprises polyester fibres.
3. A material according to claim 1, wherein the adhesive binder is a polyester.
4. A material according to claim 1, wherein the lofted or loftable, particle-bonded nonwoven constitutes one phase of a multiphase nonwoven material that includes a non-loftable nonwoven phase.
5. A material according to claim 1, wherein the functional particles comprise or consist of a liquid-absorbent polymer.
6. A material according to claim 5, wherein the liquid-absorbent polymer is a superabsorbent polymer.
7. A material according to claim 5, wherein the liquid-absorbent polymer is a homopolymer or copolymer of acrylic acid or of an acrylic acid derivative.
8. A material according to claim 1, wherein the functional particles are distributed substantially evenly throughout the fibrous matrix.
9. A material according to claim 1, wherein there is a differential distribution of the functional particles through the fibrous matrix.
10. A process for producing a nonwoven material, wherein functional particles are distributed within a matrix of fibres containing an adhesive binder, said matrix forming a lofted particle-bonded nonwoven, and at least some of the functional particles contact the adhesive binder while the latter is in a molten or softened state.
11. A process according to claim 10, wherein the functional particles are applied to a loftable, particle-bonded nonwoven, and the nonwoven is thereafter subjected to heat so that it undergoes lofting.
12. A process according to claim 10 or 11, wherein the nonwoven is cooled in its lofted state.
13. A process according to claim 10 or 11, wherein the lofted material is subjected to sufficient pressure to compact it into a denser, loftable material.
14. A process according to claim 10, wherein said matrix comprises polyester fibres, said adhesive binder is a polyester, and said functional particles comprise a liquid-absorbent polymer.
15. A process according to claim 10, wherein said lofted particle-bonded nonwoven constitutes one phase of a multiphase nonwoven material that includes a non-loftable nonwoven phase.
16. A disposable, semi-durable or durable absorbent product that comprises a nonwoven material according to claim 1.
17. A nonwoven material according to claim 1, that comprises a loftable nonwoven consisting essentially of particle-bonded crimped fibres or a lofted nonwoven formed by the heat treatment of a precursor consisting essentially of particle-bonded crimped fibres.
18. A process according to claim 10, wherein said lofted nonwoven is formed from a precursor consisting essentially of particle-bonded crimped fibres.
19. A disposable absorbent product according to claim 16 in the form of a baby's napkin, an incontinence pad for adult use, a catamenial, a bandage, a medical dressing or a wipe.
CA 572536 1987-07-27 1988-07-20 Nonwoven materials Expired - Lifetime CA1308241C (en)

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GB8717729A GB8717729D0 (en) 1987-07-27 1987-07-27 Non-woven materials
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CA (1) CA1308241C (en)
DK (1) DK416188A (en)
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GB (1) GB8717729D0 (en)

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DK416188A (en) 1989-01-28
GB8717729D0 (en) 1987-09-03
FI883216A0 (en) 1988-07-05
FI883216A (en) 1989-01-28
EP0301772A3 (en) 1990-05-23
US5041104A (en) 1991-08-20
EP0301772A2 (en) 1989-02-01
JPS6440651A (en) 1989-02-10
DK416188D0 (en) 1988-07-25

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