CA2202055C - Process to provide material connections for absorbent articles by soldering - Google Patents
Process to provide material connections for absorbent articles by soldering Download PDFInfo
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- CA2202055C CA2202055C CA 2202055 CA2202055A CA2202055C CA 2202055 C CA2202055 C CA 2202055C CA 2202055 CA2202055 CA 2202055 CA 2202055 A CA2202055 A CA 2202055A CA 2202055 C CA2202055 C CA 2202055C
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Landscapes
- Orthopedics, Nursing, And Contraception (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Abstract
The present invention relates to a process for providing connections of the materials making up disposable absorbent articles. In particular baby diapers, incontinence products and sanitary napkins which are fabricated in continuous processes are beneficially held together by soldering the materials where connections of them are desired. Replacing the currenlty used technique of adhesively attaching materials by soldering materials has the benefit of having non sticky surfaces once the solder is cooled to a temperature below its solidifying temperature. This is highly desirable where the otherwise sticky surface comes into contact with the skin of users of disposable absorbent articles or could cause adhesive build up on machine parts during the manufacturing of such articles.
Description
Process to provide material connections for absorbent articles by soldering Field of the invention The present invention relates to a process for providing connections of the materials making up disposable absorbent articles. In particular baby diapers, incontinence products and sanitary napkins which are fabricated in continuous processes are beneficially held together by soldering the materials where connections of them are desired.
Background of the invention Disposable absorbent articles like baby diapers, incontinence products and sanitary napkins are typically manufactured from a series of materials. During manufacturing the articles have to be joined to each other to form the respective disposable absorbent article. The material connections created thereby have to satisfy certain requirements a key one of which is the strength of the connection. which needs to be sufficiently high to prevent the products from falling apart at least prior to disposal thereof Typically adhesives, especially hot melt adhesives have been successfully used for that purpose. A
large variety of adhesives for the different application situations occurring in the manufacturing process of disposable absorbent articles has been developed and continue to be developed.
Alternative joining methods include welding which is used between plastic materials of similar kinds allowing to create areas were the materials are fused to each other to create permanent connections.
It now has been found that an alternative method of joining materials, namely soldering, can beneficially be used in the field of absorbent articles. This method as such is known from the art of joining metals but so far has not been applied in the field of disposable absorbent articles.
A well known problem occurring when adhesively glueing materials used in disposable absorbent articles to each other is that adhesive can migrate through permeable materials. This may happen while the adhesive is applied and also thereafter. If unpermeable materials are joined to each other the stress and strain they experience can create small apertures through which the adhesive then migrates Adhesives used in the field of disposable absorbent articles are tackified to display adhesive characteristics over a broad range of temperatures. They are usually still tacky at room temperature which makes their presence on the outside of a material used in disposable absorbent articles undesirable.
It is undesirable during the manufacturing process to have adhesive on the outside of any of the materials used in disposable articles because adhesive build up, in particular sticky adhesive build up on fast moving machinery parts quickly leads to unstable process conditions. As a minimum the occurrence of these conditions require frequent cleaning or even cause disastrous material destruction leading to machine stops and reduced efficiency.
Also adhesive which may be present on the outside of disposable absorbent articles is highly undesirable for the consumer. If adhesives which are tacky at the usage temperature of these products, that is body temperature of the wearer of such products, contact the wearer's skin or garment they will usually cause residue adhesive on garments or irritation to the wearer's skin.
These drawbacks of adhesives can be overcome by the alternative process of welding. Welding of materials usually requires material similarities if not identity in order to be feasible at all. Welding also has the disadvantage of requiring very exact temperature controls in order to provide a proper bond between materials while not causing melting away of materials or so called welding holes. This problem of very tight controls or material incompatibility to welding altogether is significantly reduced with today's adhesive technology which however carries the above mentioned drawbacks. It is therefore an objective of an aspect of the present invention to provide a method allowing the joining of materials which are usually used in the art of making disposable absorbent articles as an alternative to welding and an alternative to adhesive gluing. It is another objective of an aspect of the present invention to provide an improvement in that the alternative process developed according to the present invention can be carried out at temperatures similar to those of today's adhesive materials, while eliminating the problems associated with the stickiness of adhesives below their application temperature.
These and other objectives of aspects of the present invention will become more pronounced from the further description of the invention below.
Summary of the Invention The present invention relates to a joining process to provide material connections for materials to be used in disposable absorbent articles. The disposable absorbent articles comprise an absorbent structure which has a first and a second outermost surface located on opposite sides of the absorbent structure and the process comprises the steps of - providing a first and a second material to be used in the disposable absorbent article.
- conveying the first and the second material in a direction defined as the machine direction.
- joining the first and the second material by soldering to provide a permanent connection.
The solder used in the soldering step of the present invention is a solder which is non-sticky at 20°C, preferably it is non-sticky already at 40°C. The solder application temperature typically is above the solidifying temperature of the solder.
In a preferred embodiment of the present invention the process is used to 3a of an undergarment with the side flaps extending beyond the side edge of the crotch portion of the undergarment and are folded around that side edge for additional soiling protection. Such side flaps can be rendered at least in some parts extensible for improved fit around the side edge by high speed deformation processes.
The materials used in general in the disposable absorbent articles according to the present invention are preferably moved in the machine direction at a high speed such as at a surface speed of at least 0.4 m/s and preferably of at least 1.5 m/s. This translates into a production quantity per minute of at least 120 products of 20 cm length per product or for the more preferred speed limit of at least 450 products of 20 cm length per product respectively.
The materials to be combined by soldering in the disposable absorbent articles include any combination of the liquid permeable topsheet, the backsheet, preferably a liquid impermeable material, the core and its internal individual layers (if any) as well as multiple layers forming the topsheet or the backsheet.
The combinations of materials particularly benefiting from the soldering process according to the present invention can be found in the dependent claims according to the present specification.
In accordance with one embodiment of the present invention, a joining process to provide material connections for use in disposable absorbent articles, the articles comprising an absorbent structure, the absorbent structure comprising a first and second outermost surface located on opposite sides of the absorbent structure, comprises:
(a) providing a first and a second material;
(b) conveying the first and the second material in a machine direction;
(c) joining the first and the second material by soldering to provide a permanent connection, the soldering using a solder which is non-sticky at 20°C.
Brief description of the drawings WO 96/12461 PCT/US95I13654 .
Background of the invention Disposable absorbent articles like baby diapers, incontinence products and sanitary napkins are typically manufactured from a series of materials. During manufacturing the articles have to be joined to each other to form the respective disposable absorbent article. The material connections created thereby have to satisfy certain requirements a key one of which is the strength of the connection. which needs to be sufficiently high to prevent the products from falling apart at least prior to disposal thereof Typically adhesives, especially hot melt adhesives have been successfully used for that purpose. A
large variety of adhesives for the different application situations occurring in the manufacturing process of disposable absorbent articles has been developed and continue to be developed.
Alternative joining methods include welding which is used between plastic materials of similar kinds allowing to create areas were the materials are fused to each other to create permanent connections.
It now has been found that an alternative method of joining materials, namely soldering, can beneficially be used in the field of absorbent articles. This method as such is known from the art of joining metals but so far has not been applied in the field of disposable absorbent articles.
A well known problem occurring when adhesively glueing materials used in disposable absorbent articles to each other is that adhesive can migrate through permeable materials. This may happen while the adhesive is applied and also thereafter. If unpermeable materials are joined to each other the stress and strain they experience can create small apertures through which the adhesive then migrates Adhesives used in the field of disposable absorbent articles are tackified to display adhesive characteristics over a broad range of temperatures. They are usually still tacky at room temperature which makes their presence on the outside of a material used in disposable absorbent articles undesirable.
It is undesirable during the manufacturing process to have adhesive on the outside of any of the materials used in disposable articles because adhesive build up, in particular sticky adhesive build up on fast moving machinery parts quickly leads to unstable process conditions. As a minimum the occurrence of these conditions require frequent cleaning or even cause disastrous material destruction leading to machine stops and reduced efficiency.
Also adhesive which may be present on the outside of disposable absorbent articles is highly undesirable for the consumer. If adhesives which are tacky at the usage temperature of these products, that is body temperature of the wearer of such products, contact the wearer's skin or garment they will usually cause residue adhesive on garments or irritation to the wearer's skin.
These drawbacks of adhesives can be overcome by the alternative process of welding. Welding of materials usually requires material similarities if not identity in order to be feasible at all. Welding also has the disadvantage of requiring very exact temperature controls in order to provide a proper bond between materials while not causing melting away of materials or so called welding holes. This problem of very tight controls or material incompatibility to welding altogether is significantly reduced with today's adhesive technology which however carries the above mentioned drawbacks. It is therefore an objective of an aspect of the present invention to provide a method allowing the joining of materials which are usually used in the art of making disposable absorbent articles as an alternative to welding and an alternative to adhesive gluing. It is another objective of an aspect of the present invention to provide an improvement in that the alternative process developed according to the present invention can be carried out at temperatures similar to those of today's adhesive materials, while eliminating the problems associated with the stickiness of adhesives below their application temperature.
These and other objectives of aspects of the present invention will become more pronounced from the further description of the invention below.
Summary of the Invention The present invention relates to a joining process to provide material connections for materials to be used in disposable absorbent articles. The disposable absorbent articles comprise an absorbent structure which has a first and a second outermost surface located on opposite sides of the absorbent structure and the process comprises the steps of - providing a first and a second material to be used in the disposable absorbent article.
- conveying the first and the second material in a direction defined as the machine direction.
- joining the first and the second material by soldering to provide a permanent connection.
The solder used in the soldering step of the present invention is a solder which is non-sticky at 20°C, preferably it is non-sticky already at 40°C. The solder application temperature typically is above the solidifying temperature of the solder.
In a preferred embodiment of the present invention the process is used to 3a of an undergarment with the side flaps extending beyond the side edge of the crotch portion of the undergarment and are folded around that side edge for additional soiling protection. Such side flaps can be rendered at least in some parts extensible for improved fit around the side edge by high speed deformation processes.
The materials used in general in the disposable absorbent articles according to the present invention are preferably moved in the machine direction at a high speed such as at a surface speed of at least 0.4 m/s and preferably of at least 1.5 m/s. This translates into a production quantity per minute of at least 120 products of 20 cm length per product or for the more preferred speed limit of at least 450 products of 20 cm length per product respectively.
The materials to be combined by soldering in the disposable absorbent articles include any combination of the liquid permeable topsheet, the backsheet, preferably a liquid impermeable material, the core and its internal individual layers (if any) as well as multiple layers forming the topsheet or the backsheet.
The combinations of materials particularly benefiting from the soldering process according to the present invention can be found in the dependent claims according to the present specification.
In accordance with one embodiment of the present invention, a joining process to provide material connections for use in disposable absorbent articles, the articles comprising an absorbent structure, the absorbent structure comprising a first and second outermost surface located on opposite sides of the absorbent structure, comprises:
(a) providing a first and a second material;
(b) conveying the first and the second material in a machine direction;
(c) joining the first and the second material by soldering to provide a permanent connection, the soldering using a solder which is non-sticky at 20°C.
Brief description of the drawings WO 96/12461 PCT/US95I13654 .
Figure 1 is an exploded view of a sanitary napkin made according to the present invention not showing the solder but identifying the various elements of the preferred sanitaw napkins or pang liners as representative examples of disposable absorbent articles.
Figure 2 is an alternative sanitary napkin having a layered absorbent structure.
Figure 3 is vet another alternative sanitary napkin having side flaps.
According to the present invention a disposable article for absorbing liquid by placing it adjacent a body discharge area is joined at least partially by soldering. The article has a body-facing surface, typically provided by a liquid permeable substrate of fibrous or film-like structure; a garment facing surface, preferably provided by a liquid impermeable, but breathable substrate and an absorbent structure placed between the body facing surface and the garment facing surface. The absorbent article has a longitudinal and a lateral axis and can comprise any of the components or features usual in the art including in particular side flap components and any sort of extensibility or elastication feature known in the art.
Detailed description of the invention The disposable article for absorbent liquid is described below by reference to a sanitary napkin or panty liner. However products such as adult or baby diapers or adult incontinence inserts can similarly be supplied with the characterising feature of the present invention. Three alternative preferred embodiments of a sanitary napkin or panty liner, made according to the present invention, are shown in an exploded view in Figures 1 to 3. Each of them shows a liquid permeable topsheet (2) overlaying an absorbent structure (4) which overlays a liquid impermeable backsheet (3).
Topsheet The topsheet (2) is compliant, soft feeling, an non-irritating to the wearer's skin. The topsheet also can have elastic characteristics allowing it to be stretched in one or two directions in portions of the topsheet or throughout its extension. Further, the topsheet is fluid pervious permitting fluids (e.g., menses and/or urine) to readily penetrate through-its thickness. A suitable topsheet can be manufactured from a wide range of materials such as woven and non woven materials; polymeric .__ materials such as apertured formed thermoplastic films, apertured plastic films, and hydroformed thermoplastic film; porous foams; reticulated foams; reticulated thermoplastic film; and thermoplastic scrims. Suitable woven and nonwoven materials can be comprised of natural fibers (e.g.: wood or cotton fibers), synthetic fibers (e.g.. polymeric fibers such as polyester, polypropylene, or polyethylene fibers;
or from a combination of natural and synthetic fibers.
Preferred topsheets for use in the present invention are selected from high loft nonwoven topsheet and apertured formed film topsheets. Apertured formed films are especially preferred for the topsheet because they are pervious to body exudates and yet non absorbent and have a reduced tendency to allow fluids to pass back through and rewet the wearer's skin. Thus, the surface of the formed film that is in contact with the body remains dry, thereby reducing body soiling and creating a more comfortable feel for the wearer. Suitable formed films are described in U.S. Patent 3,929,135, U.S. Patent 4,324,246, U.S. Patent 4,342,314, U.S. Patent 4,463,045, and U.S. Patent 5,006,394.
Particularly preferred microapertured formed film topsheets are disclosed in U.S. patent 4,609,518 and U.S. Patent 4,629,643. A preferred topsheet for the present invention comprises the formed film described in one or more of the above patents and marketed on sanitary napkins by The Procter & Gamble Company of Cincinnati, Ohio as "DRI-WEAVE"~
Topsheets not having a homogeneous distribution of liquid passage ways but only a portion of the topsheet comprising liquid passage ways are also contemplated by the present invention. Typically such topsheets would have the liquid passage ways oriented such that they result in a centrally permeable and peripherally impermeable topsheet for liquids.
The body surface of the formed film topsheet can be hydrophilic so as to help liquid to transfer through the topsheet faster than if the body surface was not hydrophilic In a preferred embodiment, surfactant is incorporated into the polymeric materials of the formed film topsheet such as is described in PCT-5a publication WO 93/09741. Alternatively, the body surface of the topsheet can be made hydrophilic by treating it with a surfactant such as is described in U.S.
4,950,254.
Another alternative are so called hybrid topsheets which incorporate fibrous and film like structures. Particularly useful embodiments of such hybrid topsheets are disclosed in PCT publications WO 93/09744; WO 93/11725 or WO 93/11726.
The topsheet (2) typically extends across the whole of the absorbent structure (4) but may extend outside the area coextensive with the absorbent structure (4). As indicated in Figure 1 a peripheral edge portion (20) to be used for joining the topsheet (2) to the back sheet (3) can be provided. Also the topsheet (2) can extend and form part or all of the preferred side flaps as shown and designated 52 in Figure 3.
WD 96/12461 PCT/i1S95/13654 .
When referring to the topsheet a mufti la~~er structure or a mono layer structure are contemplated. If the various layers of multilayer topsheets are joined to each other they are as such susceptible to the joining process according to the present invention.
The hybrid topsheet mentioned above is such a mufti layer design but other multilayer topsheets such as primary and secondary topsheet designs are also considered susceptible to be joined by the process according to the present invention.
Absorbent structure The absorbent structure is shown as a single entity (4) in Figure 1 to 3. It can include the following components: (a) optionally a primary fluid distribution layer preferably together with a secondary fluid distribution layer; (b) a fluid storage layer; (c) optionally a fibrous ("dusting") layer underlying the storage layer; and (d) other optional components.
a Primarv/Secondarv Fluid Distribution Layer .
One optional component of the absorbent structure according to the present invention is a primary fluid distribution layer and a secondary fluid distribution layer. The primary distribution layer typically underlies the topsheet and is in fluid communication therewith. The topsheet transfers the acquired fluid to this primary distribution layer for ultimate 'distribution to the storage layer. This transfer of fluid through the primary distribution layer occurs not only in the thickness, but also along the length and width directions of the absorbent product. The also optional but preferred secondary distribution layer typically underlies the primary distribution layer and is in fluid communication therewith. The purpose of this secondary distribution layer is to readily acquire fluid from the primary distribution layer and transfer it rapidly to the underlying storage layer. This helps the fluid capacity of the underlying storage layer to be fully utilised.
.
b Fluid Storage Laver Positioned in fluid communication with. and typically underlying the primary or secondary distribution layers, is a fluid storage layer. The fluid storage layer can comprise any usual absorbent material or combinations thereof. It preferably comprises absorbent gelling materials usually referred to as "hydrogel", "superabsorbent" " hydrocolloid" materials in combination with suitable carriers.
The absorbent gelling materials are capable of absorbing large quantities of aqueous body fluid, and are further capable of retaining such absorbed fluids under moderate pressures. The absorbent gelling materials can be dispersed homogeneously or non-homogeneously in a suitable carrier. The suitable carriers, provided they are absorbent as such, can also be used alone.
Suitable absorbent gelling materials for use herein will most often comprise a substantially water-insoluble, slightly cross linked partially neutralised, polymeric gelling material. This material forms a hydrogel upon contact with water. Such polymer materials can be prepared from polymerizable, unsaturated, acid-containing monomers. Suitable unsaturated acidic monomers for use in preparing the polymeric absorbent gelling material used in this invention include those listed in U.S. Patent 4,654,039 reissued as RE
32,649. Preferred monomers include acrylic acid methacrylic acid and 2-acrylamide-2-methyl propane sulfonic acid. Acrylic acid itself is especially preferred for preparation of the polymeric gelling material.
Suitable carriers include materials which are conventionally utilised in absorbent structures such as cellulose fibers, in the form of fluff and/or tissues.
Suitable carriers can be used together with the absorbent gelling material, however they can also be used alone or in combinations. Most preferred are tissue or tissue laminates in the content of sanitary rlapkins/panty liners.
An embodiment made according to the present invention is shown in Figure 2 where the absorbent structure (4) comprises a double layer (42) tissue laminate formed by folding the tissue onto itself. These layers can be joined by soldering both layers to each other.
. CA 02202055 2000-06-08 7a Modified cellulose fibers such as the stiffened cellulose fibers can also be used. Synthetic fibers can also be used and include those made of cellulose acetate, polyvinyl fluoride, polyvinylidene chloride, acrylics (such as Orion~), plyvinyl acetate, non-soluble polyvinyl alcohol, plyehtylene, polypropylene, polymides (such as nylon), polyesters, bicomponent fibers, tricomponent fibers, mixtures thereof and the like. Preferably, the fiber surfaces are hydrophilic or are treated to be hydrophilic. The storage layer can also include filler materials, such as Perlite, diatomaceous earth, Vermiculite, etc. that lower rewet problems.
If the absorbent gelling material is dispersed non-homogeneously in a carrier, the storage layer can nevertheless be locally homogenous i.e. have a distribution gradient in one or several directions WO 96!12461 PCT/US95l13654.
writhin the dimensions of the storage layer. Non-homogeneous distribution can also refer to laminates of carriers enclosing absorbent gelling materials partially or fully.
c Optional Fibrous ("Dusting") Layer An optional component for inclusion in the absorbent structure according to the present invention is a fibrous layer adjacent to. and t'~pically underlying the storage layer. This underlying fibrous layer is typically referred to as a "dusting" layer since it provides a substrate on which to deposit absorbent gelling material in the storage layer during manufacture of the absorbent structure.
Indeed, in those instances where the absorbent gelling material is in the form of macro structures such as fibbers, sheets or strips, this fibrous "dusting" layer need not be included. However, this "dusting" layer provides some additional fluid-handling capabilities such as rapid wicking of fluid along the length of the pad.
d Other Optional Components of the absorbent structure The absorbent structure according to the present invention can include other optional components normally present in absorbent webs. For example. a reinforcing scrim can be positioned within the respective layers, or between the respective layers, of the absorbent structure. Such reinforcing scrims should be of such configuration as to not form interfacial barriers to fluid transfer. especially if positioned between the respective layers of the absorbent structure. Given the structural integrity that usually occurs as a result of thermal bonding, reinforcing scrims are usually not required for the absorbent structures according to the present invention.
Another component which can be included in the absorbent structure according to the invention and preferably is provided close to or as part of the primary or secondary fluid distribution layer are odor control agents. Typically active carbon coated with or in addition to other odor control agents, in particular suitable zeolite or clay materials. are optionally incorporated in the absorbent structure.
These components can be incorporated in any desired form but often are included as discrete particles.
h Backsheet The backsheet (3) primarily prevents the exudates absorbed and contained in the absorbent structure from wetting articles that contact the absorbent product such as underpants, pants, pyjamas and WO 96/12461 PCT/US95/13654 .
undergarments. The backsheet (3 ) is preferably impervious to liquids (e.g. , menses and/or urine) and is preferably manufactured from a thin plastic film. although other flexible liquid impervious materials can also be used. As used herein. the term "flexible" refers to materials that are compliant and will readily conform to the general shape and contours of the human body.
The backsheet also can have elastic characteristics allowing it to stretch in one or tu~o directions.
The backsheet typically extends across the whole of the absorbent structure but may extend outside the area coextensive with the absorbent structure (4). As indicated in Figure 1 a peripheral edge portion (30), to be used for joining the backsheet (3) to the topsheet (2), can be provided. Also the backsheet can extend into and form part of or all of the preferred sideflaps as shown and designated 54 in Figure 3.
The backsheet can comprise a woven or nonwoven material, polymeric films such as thermoplastic films of polyethylene or polypropylene, or composite materials such as a film-coated nonwoven material. Preferably, the backsheet is a polyethylene film having a thickness of from about 0.012 mm (0.~ mil) to about 0.051 mm (2.0 mils).
Exemplary polyethylene films are manufactured by Clopay Corporation of Cincinnati, Ohio, under the designation P 18-0401 and by Ethyl Corporation, Visqueen Division, of Terre Haute, Indiana, under the designation XP-39385. The backsheet is preferably embossed and/or matte finished to provide a more clothlike appearance. Further, the backsheet can permit vapors to escape from the absorbent structure, i.e. be breathable, while still preventing exudates from passing through the backsheet. Also breathable backsheets comprising several layers which are joined to each other can be used and are preferably joined by the method according to the present invention.
Optional components of the absorbent structure Optionally, the absorbent product of the present invention can comprise all those components typical for the particularly intended product use. For example sanitary napkins and panty liners often and preferably comprise components such as sideflaps and panty fastening adhesives in order to improve their positioning and soiling protection performance. Especially side flaps have become very popular with consumers. They can be formed separately and joined to the main portion of the sanitary napkin by the process according to the present invention.
Alternatively the side flaps can be formed integrally and are most preferably formed integrally with the topsheet (2) and the backsheet (3) by joining the lateral side flap extensions (52,54) of topsheet (2) and backsheet (3) to each other.
The function of side flaps, whether integral or joined to the article after being formed separately.
WO 96/12461 PCT/US95/13654.
can be further improved by rendering them extensible in one or both directions parallel to the longitudinal axis ( 10) or lateral axis ( 1 I). The extensibiliW can be prodded across all or only part of the side flaps and can be achieved by joining an elastic material to the side flap (for elastication and extensibility) or pleating or ring-rolling those parts which are to be rendered extensible.
If side flaps are formed from laminates - such as those shown in Figure 3 -the soldering according to the present invention can be used particularly beneficial. It eliminates the problems associated with built up of tacky adhesive on high speed equipment parts typically used.
Leg elastication by one or several elastic strands is also common in the art of absorbent products. In general, all typically used components in absorbent products can also be comprised in the absorbent products made according to the process of the present invention.
Process steps according to the present invention The process steps of providing at least two materials for being joined in accordance with the present invention requires at least two of the materials or structural entities discussed above for sanitary napkins to be provided. Usually the materials are provided at a fairly high surface speed as roll goods but maintain their speed of converting while forming structural entities to be combined with other materials or other structural entities thereafter.
The surface speed at which these products are made and thereby at which the joining process needs to take place is preferably at least 0.4 m/s and more preferably at least 1.5 m/s. The movement is typically in the longitudinal direction which therefore is parallel to the machine direction of the absorbent articles made according to the present invention.
Movements parallel to the transverse axis ( I I ) are also possible but less often used. The key step according to the present invention is the joining of at least two of the materials provided and conveyed according to the present invention by soldering them to each other.
The soldering is considered useful only to provide permanent connections between materials since the formed structures typically have to be coherent to be useful, at least prior to disposal of the disposable absorbent articles.
The soldering should therefore withstand at least a peel strength of 0.4 N/2.5 cm. The peel strength is the strength required to peel apart the materials joined to each other on a sample strip of 2,5 cm width. A full test description is included in the following. The soldering strength can of cause not exceed the material strengths of the materials joined. Therefore an alternative to the test against O..I
WO 96/12461 PCT/US95/13654 .
N/2.5 cm can be the internal cohesion test. In this test a connection is delaminated. The soldered connection satisfies the test if the materials are destroyed.
Joining materials by soldering requires to apply a solder to one or both surfaces to be joined and bringing the surfaces into contact before the solder cools below its solidifying temperature. In order to apply the solder it is heated to a temperature above its solidifying temperature and applied in a similar fashion or the same fashion as adhesives are applied. As a matter of fact the same equipment used today for applying adhesives can be adapted to apply the solder to the respective - surface where it is needed. Methods like contact coating, roll coating, coating by spraying in random or designed patterns (such as swirl coating,) can all be used to apply the solder according to the present invention.
When bringing the surfaces to be joined together the solder contacts both surfaces intimately at a temperature above its solidifying temperature. It creates a permanent connection after cooling below the solidifying temperature. Incorporated within the word soldering according to the present invention-are methods which in the metal art are referred to as braising where the solder forms intermaterial bonds across the contact surface. While not wishing to be limited by theory it is believed that the solder forms a thin layer of intermaterial connections where the top molecular layers of the materials to be soldered to each other are involved.
In order to distinguish the solder from adhesives a stickiness test for defining a solder is described below. Adhesives can be distinguished from the solder according to this test thereby allowing to better understand and repeat the present invention.
Solder materials can be e.g. adhesive materials without the tackifier additives usually used.
Alternatively wax type materials of high coherent strength with melting points similar to those of hot melt adhesives can be employed. One such solder example is a cleaning material designated Fuller HS350 New, available from the H.B.Fuller Company, Lueneburg, Germany.
The operating temperature of this solder is about 120°C to 140°C while comparable hot melt adhesives such as Findley 990-374-b, available from Findley, Rosendaal, The Netherlands, have operating temperatures of about 135° to 145° C.
' Test methods:
All tests conducted in respect to the present invention require test conditions of 21° plus minus 1° C
and relative humidity of 50% unless stated otherwise. All test materials are conditioned at this temperature and humidity for at least 4 hours prior to the test itself.
WO 96/12461 PCT/US95/13654 . , Peel strength or peel force testing The peel strength test analyses the force required to delaminate a connection between materials r when one material is peeled from the other material at a 180 degree angle. In respect to defining a permanent connection it has been found most sensible to create a realistic sample of the soldered material connection and analyse the peel strength between the actual materials to be soldered to each other rather than attempt to standardise the materials or solder application. The test is conducted on a sample strip of 2.5 cm width having sufficient end tabs to apply the peel force equally across the whole width of the sample to be tested:
The peel strength of a soldered connection between materials is sufficient if the force required to delaminate the soldered connection is 0.4 N/2.5 cm or if the connection can withstand holding a load of 40g without delaminating.
As already indicated materials having a cohesive strength less than the required 0.4 N/2.5 cm are still considered permanently connected by soldering if the material experiences destructive failure rather than the soldered connection. Obviously this test is substantially easier in executing than the force measurement of the peel strength. It can also be used on materials having higher cohesive strength than 0.4 N/2.5 cm provided one of the materials and not the soldered connection is destroyed. Therefore in general destruction of one of the materials soldered together implies that the soldered connection was permanent.
The stickiness test The stickiness test attempts to distinguish a solder material from a tacky adhesive. Typically the distinction will be quite apparent when simply touching an open surface of a solder material versus an open surface of an adhesive. However in order to define the distinction the following test methodology has to be applied.
Principal stickiness test method steps ' -melt the test solder material to be analysed for stickiness according to the supplier instruction;
_. - apply the molton test solder material to a substrate;
- let the molton test solder material and substrate cool to the test temperature while ensuring that the open side of the test material remains untouched and is only exposed to clean air;
WO 96/12461 PCT/US95/13654 .
- apply a second substrate. the stickiness substrate. to the untouched side of the test material under a certain pressure;
- measure the force required to peel the second substrate from the first substrate.
A solder material will have a peel force of zero at the test temperature while test materials having a peel force greater than zero are not useful in the process according to the present invention.
The test material should be heated/molten to the temperature according to the manufacturers instruction of the test material. Care should be taken with test solders which undergo curing after being heated and cooled down. Even so they may appear sticky prior to heating they can be non-sticky after being applied; i.e. after curing.
The test solder material to be checked is applied to a substrate in the usual way in which adhesives would be applied. For the current test method it has been found that using a Nordson slot coater with a SOmm wide nozzle available from a Nordson, Lueneburg, Germany is useful. The solder is applied for this test in a width of at least 2.5 cm full surface coating at a speed of the first substrate of at least 0.5 m/s relative to the coating equipment. Wider coatings are acceptable while coatings of smaller width or only fractions of the width being coated (e.g. by spiral coating) are non-acceptable in the context of this test. Of course such coating patterns can be used for applying the solder in the particular application context according to the process of the present invention.
The length of the solder material applied should be sufficiently long to conduct a series of tests in order to provide at least ten samples. The individual test sample length should be no less than 10 cm. The amount of solder used according to the stickiness test method should be the same as intended to be used in the desired process according to the present invention.
A minimum quantity is however such that the test surface onto which the solder is applied is fully covered by the test solder, and amounts of 10 to 30 g/m2 have been found useful.
The first substrate onto which the solder is applied according to the test should be a polyethylene film having a thickness of between 20-~and 30 micrometers. Solders having application temperatures too high to be applied to polyethylene films will usually not be considered at all in the context of absorbent articles. Should however in a specific case a solder be considered having an application temperature so high that the polyethylene film would not be able to withstand the application of the test solder (e.g. burn through) then a polypropylene film, or in extreme cases even a polyethylene-terephthalate film can be substituted. It should however be considered that solders having a too high application temperature will not be useful in the context of disposable absorbent articles and typical application temperatures are well below 200°C, usually below 150°C, except for soldering tissue materials useful in manufacturing disposable absorbent articles.
After the solder has been applied to the substrate it is allowed to cool to the temperature at which measurements are to be taken. It has been found that one critical temperature is about 20°C since most manufacturing processes run around room temperature i.e. about 20°C. The other typically critical temperature is the body temperature of the wearer of disposable absorbent articles since according to the objectives of the present invention any stickiness of the solder to the skin of the wearer should be prevented. Including a safety margin 40°C is considered to be an adequate upper limit below which the solder material has to be non-sticky according to this stickiness test to achieve this objective. Therefore two qualities of solder can be distinguished one which is non-sticky at 20°C or below and one preferred quality which is non-sticky at 40°C or below.
The next step according to the test method is the application of a second substrate. The second substrate should extend to the full surface of the solder test samples and preferably exceed the test surface sufficiently to provide edges where it can be manipulated.
Ideally the second substrate should provide the surface onto which the solder should display its lack of stickiness. However for test standardisation two materials are considered critical.
One substrate material is a woven cotton surface. It can be obtained under the designation "white". 100% cotton weave, style # 429-W, available from Loeffler Sitter Technic GmbH, Nettersheim, Germany. The second alternative substrate material is a polyethylene film of 25 micrometer thickness available under the designation "Tacolin~ Polyethylene Film Code ST 400" available 14a from Taco Plastics, Manchester, Great Britain.
Ten samples each are tested by applying the second substrate to the open surface of the solder under a pressure of 0.4N/cm. The application of the pressure can be conducted by using a weight in accordance with the size of the test area surface area (for the minimum test surface area this weight would be 1 kg) and extending essentially to the test surface.
Upon application of the test weight care should be taken that no uneven weight distribution is introduced e.g. by tilting the weight. For the preferred solders according to the present invention the test result will not alter over a wide range of compressions of up to 4 N/cm2 or even 10 N/cm2.
WO 96/12461 PCT/US95/13654 .
The compression under which the second substrate is applied to the solder surface should be maintained for at least 30 seconds up to 1 minute. The weight is then removed and the samples are left for another 30 seconds to 1 minute.
The measurement of peel strength then can be conducted by attempting to peel one surface away from the other and measuring the required force with highly sensitive force gauges. This measurement is well known in the art to distinguish between the strength of different adhesives.
Due to the attempt to measure a zero force value (i.e. non-stickiness) the force measurement creates substantial problems in respect to the accuracy of the results. When measuring an absolute value of zero the variation, also known as measurement noise, is strongly amplified.
Therefore it has been found that the stickiness test identifying the solder is satisfied if the second substrate delaminates under its own gravitational force.
This is measured by taking the sample, preferably while touching only the outer edges of the first substrate. and turning the sample such that the second substrate is held under its own gravitational force only by the stickiness of the test solder. If the second substrate delaminates and falls off within less than 5 seconds, preferably right away, the test solder satisfies the criterium of non-stickiness Samples where the second substrate remains joined to the first substrate are not considered solder materials in the context of the present invention. For these samples a value of stickiness can be measured as indicated above. Of course great care must be taken to ensure that no other forces (e.g.
electrostatic forces) are involved in particular if the test is conducted with polyethylene films as the two substrates.
Selective solder materials Selective solder materials which are non-sticky in conjunction with particular surfaces but sticky on "other" surfaces are also contemplated according to the process of the present invention. Their use is of course limited to joining materials where the surfaces which may get into contact with the solder (such as the steel surfaces of machinery or human skin) are not any of the mentioned "other"
'surfaces.
For example the absorbent structure (4) shown in Figure 2 as having two layers (42) may employ a selective solder. The solder in this context could be e.g. sticky to human skin even after cooling down to room temperature since the absorbent structure 4 will be fully enclosed in the backsheet (3) _.--and the top sheet (2).
WO 96/12461 PCT/US95/13654 . , One material a solder can be sticky to is another layer of the same solder.
This characteristic is in line with the present invention since a layer of solder could be applied to each of the two surfaces to be joined. A certain stickiness of solder to solder even below the solidifying temperature would then c usually be welcome since it improves the permanent connection formed according to the present invention.
__ r.
Figure 2 is an alternative sanitary napkin having a layered absorbent structure.
Figure 3 is vet another alternative sanitary napkin having side flaps.
According to the present invention a disposable article for absorbing liquid by placing it adjacent a body discharge area is joined at least partially by soldering. The article has a body-facing surface, typically provided by a liquid permeable substrate of fibrous or film-like structure; a garment facing surface, preferably provided by a liquid impermeable, but breathable substrate and an absorbent structure placed between the body facing surface and the garment facing surface. The absorbent article has a longitudinal and a lateral axis and can comprise any of the components or features usual in the art including in particular side flap components and any sort of extensibility or elastication feature known in the art.
Detailed description of the invention The disposable article for absorbent liquid is described below by reference to a sanitary napkin or panty liner. However products such as adult or baby diapers or adult incontinence inserts can similarly be supplied with the characterising feature of the present invention. Three alternative preferred embodiments of a sanitary napkin or panty liner, made according to the present invention, are shown in an exploded view in Figures 1 to 3. Each of them shows a liquid permeable topsheet (2) overlaying an absorbent structure (4) which overlays a liquid impermeable backsheet (3).
Topsheet The topsheet (2) is compliant, soft feeling, an non-irritating to the wearer's skin. The topsheet also can have elastic characteristics allowing it to be stretched in one or two directions in portions of the topsheet or throughout its extension. Further, the topsheet is fluid pervious permitting fluids (e.g., menses and/or urine) to readily penetrate through-its thickness. A suitable topsheet can be manufactured from a wide range of materials such as woven and non woven materials; polymeric .__ materials such as apertured formed thermoplastic films, apertured plastic films, and hydroformed thermoplastic film; porous foams; reticulated foams; reticulated thermoplastic film; and thermoplastic scrims. Suitable woven and nonwoven materials can be comprised of natural fibers (e.g.: wood or cotton fibers), synthetic fibers (e.g.. polymeric fibers such as polyester, polypropylene, or polyethylene fibers;
or from a combination of natural and synthetic fibers.
Preferred topsheets for use in the present invention are selected from high loft nonwoven topsheet and apertured formed film topsheets. Apertured formed films are especially preferred for the topsheet because they are pervious to body exudates and yet non absorbent and have a reduced tendency to allow fluids to pass back through and rewet the wearer's skin. Thus, the surface of the formed film that is in contact with the body remains dry, thereby reducing body soiling and creating a more comfortable feel for the wearer. Suitable formed films are described in U.S. Patent 3,929,135, U.S. Patent 4,324,246, U.S. Patent 4,342,314, U.S. Patent 4,463,045, and U.S. Patent 5,006,394.
Particularly preferred microapertured formed film topsheets are disclosed in U.S. patent 4,609,518 and U.S. Patent 4,629,643. A preferred topsheet for the present invention comprises the formed film described in one or more of the above patents and marketed on sanitary napkins by The Procter & Gamble Company of Cincinnati, Ohio as "DRI-WEAVE"~
Topsheets not having a homogeneous distribution of liquid passage ways but only a portion of the topsheet comprising liquid passage ways are also contemplated by the present invention. Typically such topsheets would have the liquid passage ways oriented such that they result in a centrally permeable and peripherally impermeable topsheet for liquids.
The body surface of the formed film topsheet can be hydrophilic so as to help liquid to transfer through the topsheet faster than if the body surface was not hydrophilic In a preferred embodiment, surfactant is incorporated into the polymeric materials of the formed film topsheet such as is described in PCT-5a publication WO 93/09741. Alternatively, the body surface of the topsheet can be made hydrophilic by treating it with a surfactant such as is described in U.S.
4,950,254.
Another alternative are so called hybrid topsheets which incorporate fibrous and film like structures. Particularly useful embodiments of such hybrid topsheets are disclosed in PCT publications WO 93/09744; WO 93/11725 or WO 93/11726.
The topsheet (2) typically extends across the whole of the absorbent structure (4) but may extend outside the area coextensive with the absorbent structure (4). As indicated in Figure 1 a peripheral edge portion (20) to be used for joining the topsheet (2) to the back sheet (3) can be provided. Also the topsheet (2) can extend and form part or all of the preferred side flaps as shown and designated 52 in Figure 3.
WD 96/12461 PCT/i1S95/13654 .
When referring to the topsheet a mufti la~~er structure or a mono layer structure are contemplated. If the various layers of multilayer topsheets are joined to each other they are as such susceptible to the joining process according to the present invention.
The hybrid topsheet mentioned above is such a mufti layer design but other multilayer topsheets such as primary and secondary topsheet designs are also considered susceptible to be joined by the process according to the present invention.
Absorbent structure The absorbent structure is shown as a single entity (4) in Figure 1 to 3. It can include the following components: (a) optionally a primary fluid distribution layer preferably together with a secondary fluid distribution layer; (b) a fluid storage layer; (c) optionally a fibrous ("dusting") layer underlying the storage layer; and (d) other optional components.
a Primarv/Secondarv Fluid Distribution Layer .
One optional component of the absorbent structure according to the present invention is a primary fluid distribution layer and a secondary fluid distribution layer. The primary distribution layer typically underlies the topsheet and is in fluid communication therewith. The topsheet transfers the acquired fluid to this primary distribution layer for ultimate 'distribution to the storage layer. This transfer of fluid through the primary distribution layer occurs not only in the thickness, but also along the length and width directions of the absorbent product. The also optional but preferred secondary distribution layer typically underlies the primary distribution layer and is in fluid communication therewith. The purpose of this secondary distribution layer is to readily acquire fluid from the primary distribution layer and transfer it rapidly to the underlying storage layer. This helps the fluid capacity of the underlying storage layer to be fully utilised.
.
b Fluid Storage Laver Positioned in fluid communication with. and typically underlying the primary or secondary distribution layers, is a fluid storage layer. The fluid storage layer can comprise any usual absorbent material or combinations thereof. It preferably comprises absorbent gelling materials usually referred to as "hydrogel", "superabsorbent" " hydrocolloid" materials in combination with suitable carriers.
The absorbent gelling materials are capable of absorbing large quantities of aqueous body fluid, and are further capable of retaining such absorbed fluids under moderate pressures. The absorbent gelling materials can be dispersed homogeneously or non-homogeneously in a suitable carrier. The suitable carriers, provided they are absorbent as such, can also be used alone.
Suitable absorbent gelling materials for use herein will most often comprise a substantially water-insoluble, slightly cross linked partially neutralised, polymeric gelling material. This material forms a hydrogel upon contact with water. Such polymer materials can be prepared from polymerizable, unsaturated, acid-containing monomers. Suitable unsaturated acidic monomers for use in preparing the polymeric absorbent gelling material used in this invention include those listed in U.S. Patent 4,654,039 reissued as RE
32,649. Preferred monomers include acrylic acid methacrylic acid and 2-acrylamide-2-methyl propane sulfonic acid. Acrylic acid itself is especially preferred for preparation of the polymeric gelling material.
Suitable carriers include materials which are conventionally utilised in absorbent structures such as cellulose fibers, in the form of fluff and/or tissues.
Suitable carriers can be used together with the absorbent gelling material, however they can also be used alone or in combinations. Most preferred are tissue or tissue laminates in the content of sanitary rlapkins/panty liners.
An embodiment made according to the present invention is shown in Figure 2 where the absorbent structure (4) comprises a double layer (42) tissue laminate formed by folding the tissue onto itself. These layers can be joined by soldering both layers to each other.
. CA 02202055 2000-06-08 7a Modified cellulose fibers such as the stiffened cellulose fibers can also be used. Synthetic fibers can also be used and include those made of cellulose acetate, polyvinyl fluoride, polyvinylidene chloride, acrylics (such as Orion~), plyvinyl acetate, non-soluble polyvinyl alcohol, plyehtylene, polypropylene, polymides (such as nylon), polyesters, bicomponent fibers, tricomponent fibers, mixtures thereof and the like. Preferably, the fiber surfaces are hydrophilic or are treated to be hydrophilic. The storage layer can also include filler materials, such as Perlite, diatomaceous earth, Vermiculite, etc. that lower rewet problems.
If the absorbent gelling material is dispersed non-homogeneously in a carrier, the storage layer can nevertheless be locally homogenous i.e. have a distribution gradient in one or several directions WO 96!12461 PCT/US95l13654.
writhin the dimensions of the storage layer. Non-homogeneous distribution can also refer to laminates of carriers enclosing absorbent gelling materials partially or fully.
c Optional Fibrous ("Dusting") Layer An optional component for inclusion in the absorbent structure according to the present invention is a fibrous layer adjacent to. and t'~pically underlying the storage layer. This underlying fibrous layer is typically referred to as a "dusting" layer since it provides a substrate on which to deposit absorbent gelling material in the storage layer during manufacture of the absorbent structure.
Indeed, in those instances where the absorbent gelling material is in the form of macro structures such as fibbers, sheets or strips, this fibrous "dusting" layer need not be included. However, this "dusting" layer provides some additional fluid-handling capabilities such as rapid wicking of fluid along the length of the pad.
d Other Optional Components of the absorbent structure The absorbent structure according to the present invention can include other optional components normally present in absorbent webs. For example. a reinforcing scrim can be positioned within the respective layers, or between the respective layers, of the absorbent structure. Such reinforcing scrims should be of such configuration as to not form interfacial barriers to fluid transfer. especially if positioned between the respective layers of the absorbent structure. Given the structural integrity that usually occurs as a result of thermal bonding, reinforcing scrims are usually not required for the absorbent structures according to the present invention.
Another component which can be included in the absorbent structure according to the invention and preferably is provided close to or as part of the primary or secondary fluid distribution layer are odor control agents. Typically active carbon coated with or in addition to other odor control agents, in particular suitable zeolite or clay materials. are optionally incorporated in the absorbent structure.
These components can be incorporated in any desired form but often are included as discrete particles.
h Backsheet The backsheet (3) primarily prevents the exudates absorbed and contained in the absorbent structure from wetting articles that contact the absorbent product such as underpants, pants, pyjamas and WO 96/12461 PCT/US95/13654 .
undergarments. The backsheet (3 ) is preferably impervious to liquids (e.g. , menses and/or urine) and is preferably manufactured from a thin plastic film. although other flexible liquid impervious materials can also be used. As used herein. the term "flexible" refers to materials that are compliant and will readily conform to the general shape and contours of the human body.
The backsheet also can have elastic characteristics allowing it to stretch in one or tu~o directions.
The backsheet typically extends across the whole of the absorbent structure but may extend outside the area coextensive with the absorbent structure (4). As indicated in Figure 1 a peripheral edge portion (30), to be used for joining the backsheet (3) to the topsheet (2), can be provided. Also the backsheet can extend into and form part of or all of the preferred sideflaps as shown and designated 54 in Figure 3.
The backsheet can comprise a woven or nonwoven material, polymeric films such as thermoplastic films of polyethylene or polypropylene, or composite materials such as a film-coated nonwoven material. Preferably, the backsheet is a polyethylene film having a thickness of from about 0.012 mm (0.~ mil) to about 0.051 mm (2.0 mils).
Exemplary polyethylene films are manufactured by Clopay Corporation of Cincinnati, Ohio, under the designation P 18-0401 and by Ethyl Corporation, Visqueen Division, of Terre Haute, Indiana, under the designation XP-39385. The backsheet is preferably embossed and/or matte finished to provide a more clothlike appearance. Further, the backsheet can permit vapors to escape from the absorbent structure, i.e. be breathable, while still preventing exudates from passing through the backsheet. Also breathable backsheets comprising several layers which are joined to each other can be used and are preferably joined by the method according to the present invention.
Optional components of the absorbent structure Optionally, the absorbent product of the present invention can comprise all those components typical for the particularly intended product use. For example sanitary napkins and panty liners often and preferably comprise components such as sideflaps and panty fastening adhesives in order to improve their positioning and soiling protection performance. Especially side flaps have become very popular with consumers. They can be formed separately and joined to the main portion of the sanitary napkin by the process according to the present invention.
Alternatively the side flaps can be formed integrally and are most preferably formed integrally with the topsheet (2) and the backsheet (3) by joining the lateral side flap extensions (52,54) of topsheet (2) and backsheet (3) to each other.
The function of side flaps, whether integral or joined to the article after being formed separately.
WO 96/12461 PCT/US95/13654.
can be further improved by rendering them extensible in one or both directions parallel to the longitudinal axis ( 10) or lateral axis ( 1 I). The extensibiliW can be prodded across all or only part of the side flaps and can be achieved by joining an elastic material to the side flap (for elastication and extensibility) or pleating or ring-rolling those parts which are to be rendered extensible.
If side flaps are formed from laminates - such as those shown in Figure 3 -the soldering according to the present invention can be used particularly beneficial. It eliminates the problems associated with built up of tacky adhesive on high speed equipment parts typically used.
Leg elastication by one or several elastic strands is also common in the art of absorbent products. In general, all typically used components in absorbent products can also be comprised in the absorbent products made according to the process of the present invention.
Process steps according to the present invention The process steps of providing at least two materials for being joined in accordance with the present invention requires at least two of the materials or structural entities discussed above for sanitary napkins to be provided. Usually the materials are provided at a fairly high surface speed as roll goods but maintain their speed of converting while forming structural entities to be combined with other materials or other structural entities thereafter.
The surface speed at which these products are made and thereby at which the joining process needs to take place is preferably at least 0.4 m/s and more preferably at least 1.5 m/s. The movement is typically in the longitudinal direction which therefore is parallel to the machine direction of the absorbent articles made according to the present invention.
Movements parallel to the transverse axis ( I I ) are also possible but less often used. The key step according to the present invention is the joining of at least two of the materials provided and conveyed according to the present invention by soldering them to each other.
The soldering is considered useful only to provide permanent connections between materials since the formed structures typically have to be coherent to be useful, at least prior to disposal of the disposable absorbent articles.
The soldering should therefore withstand at least a peel strength of 0.4 N/2.5 cm. The peel strength is the strength required to peel apart the materials joined to each other on a sample strip of 2,5 cm width. A full test description is included in the following. The soldering strength can of cause not exceed the material strengths of the materials joined. Therefore an alternative to the test against O..I
WO 96/12461 PCT/US95/13654 .
N/2.5 cm can be the internal cohesion test. In this test a connection is delaminated. The soldered connection satisfies the test if the materials are destroyed.
Joining materials by soldering requires to apply a solder to one or both surfaces to be joined and bringing the surfaces into contact before the solder cools below its solidifying temperature. In order to apply the solder it is heated to a temperature above its solidifying temperature and applied in a similar fashion or the same fashion as adhesives are applied. As a matter of fact the same equipment used today for applying adhesives can be adapted to apply the solder to the respective - surface where it is needed. Methods like contact coating, roll coating, coating by spraying in random or designed patterns (such as swirl coating,) can all be used to apply the solder according to the present invention.
When bringing the surfaces to be joined together the solder contacts both surfaces intimately at a temperature above its solidifying temperature. It creates a permanent connection after cooling below the solidifying temperature. Incorporated within the word soldering according to the present invention-are methods which in the metal art are referred to as braising where the solder forms intermaterial bonds across the contact surface. While not wishing to be limited by theory it is believed that the solder forms a thin layer of intermaterial connections where the top molecular layers of the materials to be soldered to each other are involved.
In order to distinguish the solder from adhesives a stickiness test for defining a solder is described below. Adhesives can be distinguished from the solder according to this test thereby allowing to better understand and repeat the present invention.
Solder materials can be e.g. adhesive materials without the tackifier additives usually used.
Alternatively wax type materials of high coherent strength with melting points similar to those of hot melt adhesives can be employed. One such solder example is a cleaning material designated Fuller HS350 New, available from the H.B.Fuller Company, Lueneburg, Germany.
The operating temperature of this solder is about 120°C to 140°C while comparable hot melt adhesives such as Findley 990-374-b, available from Findley, Rosendaal, The Netherlands, have operating temperatures of about 135° to 145° C.
' Test methods:
All tests conducted in respect to the present invention require test conditions of 21° plus minus 1° C
and relative humidity of 50% unless stated otherwise. All test materials are conditioned at this temperature and humidity for at least 4 hours prior to the test itself.
WO 96/12461 PCT/US95/13654 . , Peel strength or peel force testing The peel strength test analyses the force required to delaminate a connection between materials r when one material is peeled from the other material at a 180 degree angle. In respect to defining a permanent connection it has been found most sensible to create a realistic sample of the soldered material connection and analyse the peel strength between the actual materials to be soldered to each other rather than attempt to standardise the materials or solder application. The test is conducted on a sample strip of 2.5 cm width having sufficient end tabs to apply the peel force equally across the whole width of the sample to be tested:
The peel strength of a soldered connection between materials is sufficient if the force required to delaminate the soldered connection is 0.4 N/2.5 cm or if the connection can withstand holding a load of 40g without delaminating.
As already indicated materials having a cohesive strength less than the required 0.4 N/2.5 cm are still considered permanently connected by soldering if the material experiences destructive failure rather than the soldered connection. Obviously this test is substantially easier in executing than the force measurement of the peel strength. It can also be used on materials having higher cohesive strength than 0.4 N/2.5 cm provided one of the materials and not the soldered connection is destroyed. Therefore in general destruction of one of the materials soldered together implies that the soldered connection was permanent.
The stickiness test The stickiness test attempts to distinguish a solder material from a tacky adhesive. Typically the distinction will be quite apparent when simply touching an open surface of a solder material versus an open surface of an adhesive. However in order to define the distinction the following test methodology has to be applied.
Principal stickiness test method steps ' -melt the test solder material to be analysed for stickiness according to the supplier instruction;
_. - apply the molton test solder material to a substrate;
- let the molton test solder material and substrate cool to the test temperature while ensuring that the open side of the test material remains untouched and is only exposed to clean air;
WO 96/12461 PCT/US95/13654 .
- apply a second substrate. the stickiness substrate. to the untouched side of the test material under a certain pressure;
- measure the force required to peel the second substrate from the first substrate.
A solder material will have a peel force of zero at the test temperature while test materials having a peel force greater than zero are not useful in the process according to the present invention.
The test material should be heated/molten to the temperature according to the manufacturers instruction of the test material. Care should be taken with test solders which undergo curing after being heated and cooled down. Even so they may appear sticky prior to heating they can be non-sticky after being applied; i.e. after curing.
The test solder material to be checked is applied to a substrate in the usual way in which adhesives would be applied. For the current test method it has been found that using a Nordson slot coater with a SOmm wide nozzle available from a Nordson, Lueneburg, Germany is useful. The solder is applied for this test in a width of at least 2.5 cm full surface coating at a speed of the first substrate of at least 0.5 m/s relative to the coating equipment. Wider coatings are acceptable while coatings of smaller width or only fractions of the width being coated (e.g. by spiral coating) are non-acceptable in the context of this test. Of course such coating patterns can be used for applying the solder in the particular application context according to the process of the present invention.
The length of the solder material applied should be sufficiently long to conduct a series of tests in order to provide at least ten samples. The individual test sample length should be no less than 10 cm. The amount of solder used according to the stickiness test method should be the same as intended to be used in the desired process according to the present invention.
A minimum quantity is however such that the test surface onto which the solder is applied is fully covered by the test solder, and amounts of 10 to 30 g/m2 have been found useful.
The first substrate onto which the solder is applied according to the test should be a polyethylene film having a thickness of between 20-~and 30 micrometers. Solders having application temperatures too high to be applied to polyethylene films will usually not be considered at all in the context of absorbent articles. Should however in a specific case a solder be considered having an application temperature so high that the polyethylene film would not be able to withstand the application of the test solder (e.g. burn through) then a polypropylene film, or in extreme cases even a polyethylene-terephthalate film can be substituted. It should however be considered that solders having a too high application temperature will not be useful in the context of disposable absorbent articles and typical application temperatures are well below 200°C, usually below 150°C, except for soldering tissue materials useful in manufacturing disposable absorbent articles.
After the solder has been applied to the substrate it is allowed to cool to the temperature at which measurements are to be taken. It has been found that one critical temperature is about 20°C since most manufacturing processes run around room temperature i.e. about 20°C. The other typically critical temperature is the body temperature of the wearer of disposable absorbent articles since according to the objectives of the present invention any stickiness of the solder to the skin of the wearer should be prevented. Including a safety margin 40°C is considered to be an adequate upper limit below which the solder material has to be non-sticky according to this stickiness test to achieve this objective. Therefore two qualities of solder can be distinguished one which is non-sticky at 20°C or below and one preferred quality which is non-sticky at 40°C or below.
The next step according to the test method is the application of a second substrate. The second substrate should extend to the full surface of the solder test samples and preferably exceed the test surface sufficiently to provide edges where it can be manipulated.
Ideally the second substrate should provide the surface onto which the solder should display its lack of stickiness. However for test standardisation two materials are considered critical.
One substrate material is a woven cotton surface. It can be obtained under the designation "white". 100% cotton weave, style # 429-W, available from Loeffler Sitter Technic GmbH, Nettersheim, Germany. The second alternative substrate material is a polyethylene film of 25 micrometer thickness available under the designation "Tacolin~ Polyethylene Film Code ST 400" available 14a from Taco Plastics, Manchester, Great Britain.
Ten samples each are tested by applying the second substrate to the open surface of the solder under a pressure of 0.4N/cm. The application of the pressure can be conducted by using a weight in accordance with the size of the test area surface area (for the minimum test surface area this weight would be 1 kg) and extending essentially to the test surface.
Upon application of the test weight care should be taken that no uneven weight distribution is introduced e.g. by tilting the weight. For the preferred solders according to the present invention the test result will not alter over a wide range of compressions of up to 4 N/cm2 or even 10 N/cm2.
WO 96/12461 PCT/US95/13654 .
The compression under which the second substrate is applied to the solder surface should be maintained for at least 30 seconds up to 1 minute. The weight is then removed and the samples are left for another 30 seconds to 1 minute.
The measurement of peel strength then can be conducted by attempting to peel one surface away from the other and measuring the required force with highly sensitive force gauges. This measurement is well known in the art to distinguish between the strength of different adhesives.
Due to the attempt to measure a zero force value (i.e. non-stickiness) the force measurement creates substantial problems in respect to the accuracy of the results. When measuring an absolute value of zero the variation, also known as measurement noise, is strongly amplified.
Therefore it has been found that the stickiness test identifying the solder is satisfied if the second substrate delaminates under its own gravitational force.
This is measured by taking the sample, preferably while touching only the outer edges of the first substrate. and turning the sample such that the second substrate is held under its own gravitational force only by the stickiness of the test solder. If the second substrate delaminates and falls off within less than 5 seconds, preferably right away, the test solder satisfies the criterium of non-stickiness Samples where the second substrate remains joined to the first substrate are not considered solder materials in the context of the present invention. For these samples a value of stickiness can be measured as indicated above. Of course great care must be taken to ensure that no other forces (e.g.
electrostatic forces) are involved in particular if the test is conducted with polyethylene films as the two substrates.
Selective solder materials Selective solder materials which are non-sticky in conjunction with particular surfaces but sticky on "other" surfaces are also contemplated according to the process of the present invention. Their use is of course limited to joining materials where the surfaces which may get into contact with the solder (such as the steel surfaces of machinery or human skin) are not any of the mentioned "other"
'surfaces.
For example the absorbent structure (4) shown in Figure 2 as having two layers (42) may employ a selective solder. The solder in this context could be e.g. sticky to human skin even after cooling down to room temperature since the absorbent structure 4 will be fully enclosed in the backsheet (3) _.--and the top sheet (2).
WO 96/12461 PCT/US95/13654 . , One material a solder can be sticky to is another layer of the same solder.
This characteristic is in line with the present invention since a layer of solder could be applied to each of the two surfaces to be joined. A certain stickiness of solder to solder even below the solidifying temperature would then c usually be welcome since it improves the permanent connection formed according to the present invention.
__ r.
Claims (16)
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A joining process to provide material connections for use in disposable absorbent articles, said articles comprising an absorbent structure, said absorbent structure comprising a first and a second outermost surface located on opposite sides of said absorbent structure, said process comprising the steps of:
(a) providing a first and a second material;
(b) conveying said first and said second material in a machine direction;
(c) joining said first and said second material by soldering to provide a permanent connection, said soldering using a solder which is non-sticky at 20 °C.
(a) providing a first and a second material;
(b) conveying said first and said second material in a machine direction;
(c) joining said first and said second material by soldering to provide a permanent connection, said soldering using a solder which is non-sticky at 20 °C.
2. A process according to claim 1 wherein said materials have a surface speed of at least 0.4m/s, preferably at least 1.5m/s, in machine direction.
3. A process according to any one of the preceding claims wherein said first material is a liquid permeable topsheet and said second material is a backsheet.
4. A process according to claim 3 wherein said topsheet and said backsheet comprise a peripheral edge portion extending beyond the periphery of said absorbent structure and said soldering joins said backsheet to said topsheet in at least part of said peripheral edge portion.
5. A process according to claim 4 wherein said soldering joins said backsheet to said topsheet along the whole peripheral edge portion.
6. A process according to any one of claims 1 to 2 wherein said first material is a liquid permeable topsheet and said second material is said absorbent structure and said topsheet and said absorbent structure are joined across said first outermost surface.
7. A process according to any one of claims 1 to 2 wherein said first material is a first layer of a multi-layer, liquid permeable topsheet and said second material is a second layer of a multi-layer, liquid permeable topsheet.
8. A process according to any one of claims 1 to 2 wherein said first material is a breathable backsheet and said second material is said absorbent structure and said backsheet and said absorbent structure are joined across said second outermost surface.
9. A process according to any one of claims 1 to 2 wherein said first material is a first layer of a multi-layer backsheet and said second material is a second layer of a multi-layer backsheet.
10. A process according to any one of claims 1 to 3 or 9 wherein said backsheet is liquid impermeable.
11. A process according to any one of claims 1 to 2 wherein said absorbent structure comprises multiple layers and said first material is a first layer of said absorbent structure and said second material is a second layer of said absorbent structure.
12. A process according to claim 9 wherein said absorbent structure comprises a tissue laminate joined by soldering a first tissue layer to a second tissue layer.
13. A process according to claim 12 wherein said first tissue layer and said second tissue layer are provided by folding a tissue upon itself.
14. A process according to any one of the preceding claims wherein said soldering uses a solder which is non-sticky at 40 °C.
15. A process according to any one of the preceding claims wherein said disposable absorbent articles are sanitary napkins or panty liners used in the crotch portion of an undergarment.
16. A process according to claim 15 wherein said articles have side flaps extending beyond and wrapping around the side edge of the crotch portion of said undergarment.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP94203040.4 | 1994-10-20 | ||
| EP94203040A EP0707841B2 (en) | 1994-10-20 | 1994-10-20 | Process to provide material connections for absorbent articles by soldering |
| PCT/US1995/013654 WO1996012461A1 (en) | 1994-10-20 | 1995-10-19 | Process to provide material connections for absorbent articles by soldering |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2202055A1 CA2202055A1 (en) | 1996-05-02 |
| CA2202055C true CA2202055C (en) | 2000-08-29 |
Family
ID=29421921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2202055 Expired - Fee Related CA2202055C (en) | 1994-10-20 | 1995-10-19 | Process to provide material connections for absorbent articles by soldering |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2202055C (en) |
-
1995
- 1995-10-19 CA CA 2202055 patent/CA2202055C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2202055A1 (en) | 1996-05-02 |
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