NZ716077B2 - An absorbent composite, an absorbent article employing the same, and methods, systems, and apparatus for making the absorbent composite and/or article - Google Patents
An absorbent composite, an absorbent article employing the same, and methods, systems, and apparatus for making the absorbent composite and/or article Download PDFInfo
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- NZ716077B2 NZ716077B2 NZ716077A NZ71607714A NZ716077B2 NZ 716077 B2 NZ716077 B2 NZ 716077B2 NZ 716077 A NZ716077 A NZ 716077A NZ 71607714 A NZ71607714 A NZ 71607714A NZ 716077 B2 NZ716077 B2 NZ 716077B2
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- absorbent
- sap
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Abstract
The present invention provides an absorbent core composite for incorporation into a disposable absorbent article, the absorbent core composite comprising: a first material layer having an outside surface forming a bodyside outer surface of the absorbent core composite; a second material layer having an outside surface forming an opposite outer surface of said absorbent core composite, wherein the first material layer is a nonwoven having a density of from 0.01 to 0.03 g/cc and the second material layer is a nonwoven having a density that is higher than the density of the first material layer; and a first layer of absorbent particles disposed between said outer surfaces of the absorbent composite and having a first average size dimension; a second layer of absorbent particles disposed between said outer surfaces of the absorbent composite, said absorbent particles of said second layer having a second average size dimension that is less than the first average size dimension of the first layer of absorbent particles; and wherein said first layer of absorbent particles are situated substantially in the first material layer and the second layer of absorbent particles are situated substantially in the second material layer. ving an outside surface forming an opposite outer surface of said absorbent core composite, wherein the first material layer is a nonwoven having a density of from 0.01 to 0.03 g/cc and the second material layer is a nonwoven having a density that is higher than the density of the first material layer; and a first layer of absorbent particles disposed between said outer surfaces of the absorbent composite and having a first average size dimension; a second layer of absorbent particles disposed between said outer surfaces of the absorbent composite, said absorbent particles of said second layer having a second average size dimension that is less than the first average size dimension of the first layer of absorbent particles; and wherein said first layer of absorbent particles are situated substantially in the first material layer and the second layer of absorbent particles are situated substantially in the second material layer.
Description
AN ABSORBENT COMPOSITE, AN ABSORBENT E EMPLOYING THE
SAME, AND METHODS, SYSTEMS, AND TUS FOR MAKING THE
ABSORBENT COMPOSITE AND/OR ARTICLE
The present application claims the benefit of United States Provisional Application
Serial No. ,961 filed on July 3, 2013 (pending) and United States Provisional
Application No. 61/843,986 filed on July 9, 2013 (pending). Each of these disclosures is
hereby orated by reference for all purposes and made a part of the present disclosure.
[002] The present disclosure relates generally to an absorbent core composite and
disposable absorbent garment incorporating the core composite. The disclosure also relates
to a system, apparatus, and a method of making the absorbent composite or the disposable
absorbent article. Such disposable absorbent articles include diapers, ng pants, adult
incontinence products, bodily exudates absorbing products, ne hygiene products, and
other absorbent products (collectively sable absorbent articles").
Prior disposable absorbent articles typically employ three basic structural ts: a
topsheet that forms the inner surface, a eet that forms the outer surface, and an
absorbent core that is interposed between the topsheet and the backsheet. The topsheet is
designed to allow liquid to pass from outside the absorbent article through the topsheet and
into the absorbent core. The et may be made out of a range of liquid and vapor
permeable hydrophilic or hydrophobic materials.
The backsheet is designed to t fluid from passing from the absorbent core
through the backsheet and out of the absorbent article. The backsheet may be made out of an
eable film that extends the filll width of the article or a combination of cloth-like
material and impermeable film. The backsheet may also have vapor transmission properties
("breathability") that allow vapor to pass through the backsheet t releasing fluid stored
in the absorbent core. The backsheet may also be made from a liquid impermeable but vapor
transmittable non-woven material such as spunbond, melt-blow, ond ); spun-
bond, melt-blown, melt-blown, spun-bond ("SMMS"); micro, nano, or splitable fibers; spun
melt or spun laced; carded; and the like.
The absorbent core is designed to contain and distribute fluid that passes through the
topsheet. A typical absorbent core is made out of a high or super absorbent polymer (SAP)
ized by an absorbent matrix. SAP is commonly made out of materials such as polyvinyl
alcohol, polyacrylates, various grafted starches, and cross-linked sodium polyacrylate. SAP
can be in the form of particles, fibers, foams, web, spheres, agglomerates of regular or
irregular shapes, and film. The ent matrix is typically a de-f1berized wood pulp or
similar material. The absorbent matrix is very bulky relative to the topsheet, backsheet, and
SAP. Most of a diaper's thickness comes from the absorbent core.
Increasingly, consumers of absorbent articles are demanding thinner absorbent
articles. To meet these demands, manufactures are decreasing the thickness of ent
articles by decreasing the amount of absorbent matrix used in absorbent cores. Although the
resulting absorbent cores are thinner, they suffer in performance. As the amount of absorbent
matrix is reduced, it is less effective in stabilizing the SAP - preventing the SAP from
migrating within the absorbent core. As SAP migrates within the core, the absorbent core
loses its effectiveness and no longer has uniform absorbency. For example, SAP that is not
contained tends to bunch up in wetted areas and is inefficient for ng subsequent
discharges.
Manufacturers have attempted to solve this problem by ng small, individual SAP
pockets or by gluing the SAP. These ons, however, have been largely unsuccessful. The
SAP s merely limit the ion to movement within the pockets. However, because
there is still a movement of the particles, the absorbent core does not t uniform
absorbency. Gluing the SAP izes the SAP, but results in an uncomfortably stiff
absorbent core and a loss in the SAP's swelling capacity.
Securing the SAP by adhesive, cover layer, or other manner can also affect the
performance of the SAP during product use. In some instances, SAP and product
performance are sacrificed for core stability and ease of manufacture. Because the ent
core is pressed against the user's skin during e use, the wearer is very sensitive to the
touch and feel of the core. Thus, the introduction of even a minor physical feature in an
absorbent core design can have a great impact on the comfort of the user.
[009] There is a continuing need for an improved ent product featuring reduced
composite thickness, but maintaining or improving fluid handling properties and sure fit and
comfort. The specifications ofUS. Pat. No. 8,148,598 and International Application
(the '051 Application), each of which is commonly assigned and
designates at least one common inventor as the present application, describes a prior
improvement to the state of the art and serves as background to the present disclosure. The
disclosures both documents are hereby incorporated by reference, in its entirety, for all
purposes and made a part of the present disclosure. The t disclosure may, in one
respect, be regarded as continuing and fiarthering the effort to provide improved ent
products and systems, apparatus, and methods of manufacturing.
BRIEF SUMMARY
The present disclosure relates generally to an ent core composite and
disposable absorbent t orating the absorbent composite. The disclosure also
relates to a system, apparatus, and a method of making the absorbent composite or the
disposable absorbent article. In one aspect, improved absorbent core ites are provided
with advantageous swell capacities or void volumes. In another aspect, absorbent core
composites (and methods and systems of making same) are provided with void volume
increase mechanisms, configurations, or structures. Such functionalities are preferably
triggered or activated during use, prior use, or during manufacture. In yet another aspect,
absorbent core composites are provided with improved liquid t, retention, and
distribution functionalities, as well as manufacturability.
In one aspect, an ent core composite is disclosed for incorporation into a
disposable absorbent article. The ent core composite include a first material layer
(preferably en) and a second material layer (preferably nonwoven) at least partially
d (e.g., by bond sites, bond points, adhesive, and the like) to the first material layer to
define at least one pocket therebetween. Preferably, multiple pockets are defined, except in
the case of where a generally uniform layer or bed of absorbent is preferred or better suited
for the application. The pocket is said have a fixed l volume (e.g., as defined by its
al configuration). Further, an ate of ent particles is provided in the
pocket(s) to occupy a portion of the fixed initial volume. The absorbent particles are
preferably SAP particles and is characterized by a dry volume associated with a dry state and
a swell volume associated with a liquid saturation state. In respect to or for the , the
aggregate is characterized by a collective dry volume and a collective swell volume, wherein
the pocket has an initial configuration that retains the aggregate therein.
In another aspect, an absorbent core composite is disclosed for incorporation into a
disposable absorbent article. The absorbent core composite has a first material layer, a second
material layer at least partially secured to the first material layer to define a plurality of
pockets, each of the pockets having a fixed l volume, and absorbent particles provided in
aggregates each disposed in one of the pockets. The absorbent particles are characterized by a
dry volume associated with a dry state and swell volume associated with a liquid saturation
state, and n, for each pocket, the aggregate is characterized by a collective dry volume
and a collective swell , the collective swell volume being greater than the initial
pocket volume. Each pocket is expandable from an initial configuration partially defining the
WO 02934
initial volume toward an expanded configuration under which an increased pocket volume
accommodates the collective swell volume. For each pocket, the first material layer has a
re sensitive configuration, such that re generated by the aggregate transforming
into the collective swell volume initiates expansion of the first material layer from an initial
configuration partially defining the initial volume toward an expanded configuration under
which an increased pocket volume accommodates the collective swell volume.
In r aspect, a disposable absorbent article (e.g., a diaper, training pants, adult
incontinence articles, and the like) is disclosed having a chassis body defined by a first end
margin and a second end margin longitudinally spaced from the first end margin. The end
margins partially define front and back waist regions that are positioned about a waist of a
user during wear of the absorbent article. The article further includes a topsheet, a backsheet,
and an ent core composite ed between the topsheet and backsheet. The
composite es a first en layer, a second nonwoven layer at least partially secured
to the first nonwoven layer to define a plurality of pockets therebetween, the pockets having a
fixed initial , and an aggregate of SAP particles disposed in the pocket to occupy a
portion of the fixed initial . The SAP particles are characterized by a dry volume
associated with a dry state and a swell volume associated with a liquid saturation state, and
wherein, for the pocket, the aggregate is characterized by a collective dry volume and a
tive swell volume, wherein the pocket has an initial configuration that retains the
aggregate. Further, an outside surface of the first nonwoven layer exhibits surface
discontinuities in the initial ration of the . The outside e is extendible,
however, to substantially remove the discontinuities and place the pocket in an expanded
configuration defining an increased pocket volume. The discontinuities may be corrugations,
folds, pleats, and other (temporary) deformations that are removable upon ion of the
outside surface.
In another absorbent core composite for incorporation into a able absorbent
e, the absorbent core composite has a first material layer having an outside surface
forming a bodyside outer surface of the absorbent core composite, a second material layer
having an outside surface forming an opposite outer surface of said ent core composite,
a first layer of absorbent particles disposed between the outer surfaces of the absorbent
composite and having an average size dimension (Le. , the average width or diameter of the
particles), and a second layer of absorbent particles disposed between the outer surfaces of
the absorbent composite and having an average size dimension less than the average size
dimension of the first layer. The first layer of particles are situated substantially in the first
material layer and the second layer of particles are ed substantially in the second
material layer. In a further embodiment, an intermediate layer is disposed between the first
and second material layers and contains r layer of absorbent particles. The densities of
the two or three layers may be selected to achieve a desired gradient of absorbent particles
(and absorbent properties).
In another aspect, a method is disclosed for forming an absorbent composite for
incorporation into a able absorbent article. The method entails providing a first
material layer, positioning a second material layer beneath the second material layer,
providing a supply of absorbent les composed of a population of a first absorbent
particles having a first average size dimension and a second population of ent particles
having a second average size dimension less than the first average size dimension, and
depositing the first and second populations of absorbent particles onto the first material layer
such that absorbent particles of the first population are maintained in the first material layer
and absorbent les of the second population filter through the first material layer and
settle in the second material layer. The first material layer may be a low density nonwoven
having a density between 0.01 to 0.03 g/cc and the second material layer may be of a higher
density nonwoven.
In another aspect, r absorbent core ite is disclosed for incorporation into
a able ent article. The absorbent core composite includes a bodyside first
material layer (nonwoven), and a second material layer (nonwoven), wherein the first and
second material layers define a space therebetween. The defined space contains a layer of
superabsorbent particles, which includes a tion of SAP particles and a population of
non-SAP spacing particles that are smaller than the SAP particles and generally positioned
between two or more SAP particles, thereby spacing two or more SAP particles from one
another. Further, the spacing particles may be selected from the group of spacing particles
consisting of: inert les; water-soluble particles; volatile les; ion-exchange
particles; and combinations thereof.
In another aspect, r disposable absorbent article is disclosed having a chassis
body defined by a first end margin and a second end margin longitudinally spaced from the
first end margin, the end margins partially defining front and back waist regions that are
positioned about a waist of a user during wear of the absorbent article. The article further
includes a topsheet, a backsheet, and an absorbent composite disposed between the topsheet
and backsheet. The absorbent composite includes a first al layer having an e
surface, a second material layer having an outside surface, a first layer of absorbent particles
provided between the outside surfaces, and a second layer of absorbent particles provided
between the outside es, wherein the second layer of absorbent particles has ent
properties different from said first layer.
A method is also disclosed for making an absorbent ite for incorporation into
a disposable absorbent garment. The method entails conveying a first sheet of a first
nonwoven layer, depositing absorbent particles on the first sheet, and applying a second sheet
of a second nonwoven layer over the deposited absorbent les and first sheet, thereby
forming a composite including two material layers sandwiching absorbent particles
therebetween. The method also provides bonding the first and second material layers to
secure, at least partially, absorbent particles etween. In one ment, prior to
ing the first sheet, a surface of the first sheet is deformed to form laterally elongatable
surface discontinuities.
The sure also provides for systems and methods for making the articles and
composites discussed above or in the Detail Description, or illustrated in the Figures. It
should also be noted that various embodiments are disclosed . Some embodiments
feature elements (design features, steps or components) that are not described as being
specifically incorporated into other embodiments. Many more variations or embodiments are
contemplated, however, and such fiarther combinations or incorporation of elements will be
evident to one skilled in the art in sion of the present disclosure.
[0020] Lastly, the absorbent composite es means for altering the initial pocket
configuration during use (6.g. , in the event if liquid intake by the absorbent article) to
accommodate the swell volume of the aggregate. For example, the altering means may be
provided by the pocket being expandable from the initial configuration defining the initial
volume toward an expanded configuration under which an increased pocket volume
accommodates the collective swell volume, the collective swell volume being greater than the
collective dry . Further, such means for altering the initial pocket configuration
means at least one of the first and second material layers being elongatable in response to
ng of SAP aggregate in said pocket. The subject elongatable material layer may be
corrugated or may have a plurality of folds therein extending in the longitudinal direction.
The altering means may also be provided by a breakable substrate such as tissue, dry-crepe
tissue or a slitted substrate ned material). The altering means may, in the alternative,
be provided by breakable bonds, such as ble bond point or water-soluble adhesive, that
otherwise secure the material layers to define the (s) and contain the SAP aggregate
(i.e., during SAP swell).
BRIEF DESCRIPTION OF THE DRAWINGS
is a perspective view of a disposable absorbent e incorporating an
absorbent composite according to the present disclosure;
is a top plan view of the disposable absorbent article in , in a flat and
extended on;
is an exploded view of the disposable absorbent article in ;
is a schematic of a system for making an ent composite;
FIGS. 2A-2B is a simplified illustration of an absorbent core composite with a
plurality of pockets of aggregates of absorbent particles;
FIGS. 2C-2E are bonding patterns suitable for forming pockets in the absorbent core
composite such as those in FIGS. 2A-2B;
is an elevated sectional view of a section of an absorbent composite
having an elongatable substrate partially g a pocket SAP aggregate, according to the
t disclosure, the pocket shown first in a tivated and in a fixed initial
ration and then, activated an in an expanded configuration;
is a perspective view of a sheet of the absorbent composite in ;
is an elevated cross-sectional view of a section of an alternative absorbent
core composite having an elongatable substrate, according to the present disclosure, shown in
a pre-activated state;
is an elevated cross-sectional view of the n of an alternative absorbent
core composite in , shown in an ted or expanded state;
is an elevated cross-sectional View of a section of a diaper incorporating the
absorbent ite in ;
[0032] FIGS. 4 are simplified illustrations of portions of a process of riffling or corrugating a
non-woven sheet for incorporation into a absorbent composite, and equipment suitable for
use in the process;
FIGS. 5 are simplified illustrations of an absorbent core composite having an
elongatable substrate according to the present disclosure;
[0034] FIGS 6A-6C are simplified illustrations of multi-layer absorbent core composites,
according to the present disclosure;
FIGS 7A-7B are simplified illustrations of folded absorbent core composites
according to the present disclosure;
FIGS. 8A-8C are simplified illustrations in plan view of absorbent core composites
featuring cross-directional profiling of absorbent properties, according to the present
disclosure;
FIGS. 9A-9C are simplified diagrams illustrating the relation between travel of liquid
on an absorbent core and changes in absorbent property of the SAP in areas along said liquid
travel;
is graph showing the on between SAP absorbent capacity and target
liquid ionic strength;
FIG. B is a depiction of a bar chart displaying suitable SAP particle size
distribution;
FIG. lOC is a depiction of a bar chart displaying suitable hotmelt particle size
distribution;
FIG. ll is a simplified illustration of an absorbent composite exhibiting layered
particle size filtration on nonwoven layer;
[0042] is a simplified illustration of a SAP aggregate with and without inert particle
spacers;
is graphical chart of simplified illustrations of SAP ate constitutions
during bonding and product use;
is a simplified illustration of a system and process for making an absorbent
composite sheet having lanes of SAP, according to one embodiment;
is a simplified illustration of a system and process of making an ent
composite sheet utilizing hotmelt fibers in the composite according to one ment;
is schematic illustrating a system and process for making an absorbent
composite according to various embodiment; and
[0047] is a schematic illustrating a system and process for making an absorbent
composite according to s embodiments.
DETAILED PTION
Referring first to , a able absorbent article is shown in the form of a
diaper 10. The diaper 10 is a type of absorbent article that readily incorporates, as its central
functional component, an ent core composite according to the present sure. The
basic components of the diaper 10 are a topsheet 50, a backsheet 60, and an absorbent core 46
(not shown in but in FIGS. 1B and 1C) disposed between the eet 60 and
topsheet 50. The diaper 10 also es upstanding barrier cuffs 34 that extend
longitudinally along the diaper and are elasticized to conform to the buttocks of the wearer.
Additionally, the diaper includes an elastic waist band 52 and fastening elements 26. t
26, is ible to and engages the ponding opposing end of the diaper 10 to secure
the diaper 10 about the wearer.
illustrates a composite web structure of the diaper 10 in a generally flat and
unfolded configuration. As will be explained below, the web structure may be subsequently
trimmed, folded, sealed, welded and/or otherwise manipulated to form a disposable diaper 10
in a finished or final form. To facilitate description of the diaper 10, the description refers to a
longitudinally extending axis AA, a lly extending central axis BB, a pair of
longitudinally extending side edges 90, and a pair of end edges 92 that extend between side
edges 90. The imaginary lines AA and BB shown are also referred to as the diaper's
longitudinal and lateral centerlines, respectively. Generally, when discussing the positions or
orientations of s elements of the diaper 10, references made to lateral and longitudinal
directions or extensions relate or correspond with the axes AA and BB (unless referring
specifically to the context of that particular element). It should also be noted that the
direction of the udinal centerline AA generally corresponds with the machine direction
(MD) of the diaper 10 while the direction of the lateral centerline BB corresponds with the
cross machine direction (CD) of the diaper. The machine direction (MD) of a diaper element
such as a topheet or backsheet, and other nonwovens which contain fibrous elements, can be
determined by observing the alignment and/or condition of the fibers in the diaper element.
The fibers normally align with the machine direction. This can be observed, for example,
under a cope long after the diaper has been manufactured.
Along the longitudinal axis AA, the diaper 10 includes a first end region or front waist
region 12, a second end region or back waist region 14, and a crotch region 16 disposed
etween. Each of the front and back waist regions 12, 14 is characterized by a pair of ear
regions or ears 18, which are d on either side of a central body portion 20 and extend
laterally from the side edges 90. A fastening structure 26 (e. g., a conventional tape fastener)
is affixed to each of the ears 18 along the back waist region 14 of diaper 10. When the diaper
is worn about the waist, the front waist region 12 is fitted adjacent the front waist area of
the wearer, the back waist region 14 is fitted adjacent the back waist area, and the crotch
region 16 fits about and eath the crotch area. To properly secure the diaper 10 to the
, the ears 18 of the back waist region 14 are brought around the waist of the wearer and
toward the front and into alignment with the ears 18 of the front waist region 12.
reveals an absorbent core 46 ed beneath the topsheet 48 and an
acquisition and distribution layer (ADL) 48. is an exploded view of the diaper of
FIGS. 1A and 1B, and illustrates, in simplified form, the absorbent core 46 as a multi-
component te having a generally rectangular shape. In other preferred embodiments,
the absorbent core 46 takes on an hourglass shape featuring a laterally narrowed central
region. The absorbent core 46 is generally composed of a top nonwoven layer 70, a bottom
nonwoven layer 72, and a layer, body, or tion of absorbent materials 74 therebetween.
Prior to incorporation into the diaper, the absorbent core body 46 is often referred to as an
absorbent ite or absorbent core composite. A generally planar extension of the
ent composite may be presented and referred to as a web or an absorbent composite
sheet during manufacturing and as a product or article of cture. The present
disclosure is primarily directed to an improved absorbent composite construction and systems
and methods of making the composite or an absorbent composite sheet from which absorbent
composite is sourced. The present disclosure is also directed to a disposable absorbent article
in which the absorbent composite is incorporated as the absorbent core.
An absorbent core composite of the type addressed by certain ments of the
present disclosure features pockets or containers in which SAP is retained. Other improved
absorbent core composites are described which also exhibit improved fluid handling
performance and are amendable to thin-core constructions, but may not arily feature or
require pockets. Without pockets, these composites can be made with a generally uniform
profile and depth.
is taken from the '598 Patent and reproduced herein, in most part, to illustrate
suitable processes, subprocesses, systems, and components for making the ent
composite and/or a disposable absorbent e incorporating the composite. Certain
embodiments of the absorbent composite described herein may require modifications to the
method and system illustrated by FIG. lD. Description provided herein and/or the general
knowledge in the ry will make the required modification fairly evident, however, to
those skilled in the relevant manufacturing art.
Referring to FIG. ID, a fabric 125 is sed from roll 120 and carried along a
production line on a er belt 100. The fabric 125 is a thermo plastic material that may
be a woven, nonwoven, film, or a combination thereof. In some embodiments, the fabric 125
is secured to the conveyor belt 100 by a vacuum system 110. The vacuum system 110 serves
to conform the fabric 125 to the convey belt 100. SAP particles 135 are then deposited on the
fabric 125 by a SAP ser 130. The SAP dispenser 130 may be configured to position
SAP particles in their desired position or lanes on the first fabric or may be configured merely
to deposit SAP particles on the first fabric, whereon the SAP particles are positioned by
another means. Once SAP les have been deposited and positioned on fabric 125, a
second fabric 155 uced into the production line from roll 150 is moved into engagement
with the SAP fabric 125 web. The second fabric 155 may be selected from a variety of
materials including spun-bonded thermoplastic or similar woven or nonwoven material, film,
or combinations thereof.
In , a thermal bonding system is shown including calendar rolls 160 and 170
which are used to engage and bond fabrics 125 and 155 together . Other bonding systems
may be suitable or red depending on the application, however. For example, an
ultrasonic bonding system may be used in place of the calendar rolls to provide bond points
in many ations. The bond pattern may be d with the distribution of the SAP
particles 135. Once the fabrics are bonded to form a sheet or laminate of absorbent core
composite, the sheet may be gathered into a roll 200. In other applications, depending on the
composite application, the te may be advanced for filrther processing, including
slitting, application of additional layers, oration with or into another product or even
into a disposable absorbent e.
In one embodiment, the core composite has a top preferably nonwoven layer (fabric)
and a bottom, preferably, nonwoven layer (fabric). The two layers may be bonded or
otherwise engaged to form the pockets, as described in US. Pat. No. 8,148,598 B2 issued on
April 3, 2012, and International Application , both of which are
commonly ed. The ‘598 patent further describes a core construction employing such
pockets, which is particularly suited for containing the SAP and readily and effectively
disposing SAP material or SAP particles to perform the liquid absorbing or retention
function, and preferably, in some embodiments, without the inclusion and employment of an
absorbent matrix. In these further embodiments, the ent composite is characterized as
being fiee (or lacking) of an ent matrix e of stabilizing an absorbent layer of
les t particle migration and alternatively, as being pulpless. International
Application (the '051 application) teach further ent composite
constructions and methods of cturing that advantageously secure absorbent materials
beneath a cover layer, while also enhancing the fluid handling performance of the absorbent
materials and\or maintaining user comfort. Accordingly, the ‘disclosure of the “598 Patent
and the ‘051 application may serve as starting points and background for the core composite
constructions, absorbent articles, and manufacturing processes, and apparatus introduced
herein. The ‘598 patent and the '051 application are hereby incorporated by reference in its
entirety, and for all purposes including g as background and nce to tate
understanding and implementation of the products, systems, apparatus, and methods
described .
Absorbent core composites such as that depicted in FIGS. 2A and 2B may be made
with particularly advantageous arrangements of aggregates of absorbent particles, such as the
SAP particles. Each of the aggregates on the absorbent composite 510 is represented by the
diamond-shaped enclosure 514 in the n. In preferred embodiments, SAP is ed
as the ent particles in the aggregates. Furthermore, SAP aggregates in each of FIGS. 1
are preferably maintained in place and stabilized by physical entrapments or containers
provided by the engagement of a first fabric disposed generally above the SAP aggregate
with a second fabric disposed generally beneath the SAP aggregate. Thus, in an alternative
view, the diamond units represent the outline of the containers or pockets, reflecting in
particular embodiments, the engagement of the top fabric with the bottom fabric, as
previously described herein. The ners or pockets are also referred to as cells, herein.
The absorbent performance of the SAP can be affected by the size and structure of the
container. As SAP becomes more saturated, its permeability is reduced. Water cannot pass
through the SAP particle due to the high level of water already contained within the SAP
particle and eventually the SAP can completely halt the e of fiarther fluid through it.
This is known as gel blocking. Also, as SAP becomes more saturated, it swells and its
volume increases. By confining the SAP in a small container of fixed volume it is le to
ct the swelling of the SAP and prevent it from ng its highest saturation levels (and
by consequence stop the SAP from reaching its lowest levels of permeability). The degree to
which the SAP particle is restricted depends on a number of factors, including: the nature and
size of the container, the size and frequency of any breaks in the container (e.g., along the
side walls), the amount of SAP disposed in the container, and the amount of fluid absorbed
by the SAP. Further, the performance properties of SAP are affected by its degree of
saturation. Specifically, absorbent ite properties such as bility, absorption rate,
capillary pressure (arising from the void space in the composite) will vary significantly as the
SAP changes from dry to fully saturated. In accordance with a method of the present
disclosure, target or optimal performance of the SAP may be achieved by changing the size
of the container and/or the SAP concentration so as to physically constrain the swelling of the
SAP and limit the maximum saturation point of the SAP. By incorporating these physical
features, preferred levels of bility or a preferred tion property may be achieved
in target regions of the absorbent core. Thus, by playing with the two variables of pocket size
and the amount of SAP in the pocket, the m permeability of that container or pocket
may be "set". Pockets in some regions of the diaper may be prevented from gel blocking and
the permeability of that region of the core may be optimized. A gradient of pocket size may
also be established to obtain maximum flow and utilization of the absorbent core. This
gradient will extend from the target zone to the ends or sides of the diaper.
The various arrangements of containers or s also promote SAP and core
utilization and t fluid from bypassing the containers. Ideally, fluid should leak or flow
from container to container as the SAP s the m level of saturation which is set
either by the properties of the SAP or the volume of the pocket into which it is ing.
Applicants contemplate that, in some of the previously described composites or arrangements
of pockets, there may be a tendency for fluid to leak between the s. That is the fluid
runs rapidly along the channels formed by embossing lines and does not enter the core. Fluid
also flows through the nonwoven material, although not as rapidly as on the surface but faster
than SAP to SAP and through SAP. To mitigate this tendency, ements or patterns for
the containers are preferably ones that minimize or eliminate short and direct routes (as may
be established along embossing lines) of fluid flow from the core center to the side margins
of the core. Specifically, embossing lines for the fluid to flow along from the center of the
core to the side edge of the core. To illustrate, containers or pockets shaped as diamonds are
preferred to ones formed in squares or gles, because the diagonal lines or channels
formed by the diamond containers are longer and more circuitous. Circles are also effective if
packed in a way that does not present channels that flow quickly to the edge. In more
preferred arrangements, fluid flow is forced to change directions one or more times before
flowing through the side of the diaper.
[0060] An ent core for a baby diaper or adult incontinence product is required to
absorb fluid quickly, in an anatomically aligned region of the core, absorb all the fluid
without g at the sides or ends of the product and hold on to that fluid without wetting
the user’s skin particularly when under pressure caused by the user’s bodyweight. This is
accomplished by providing regions of the core having different performance parameters
defined by the size of the containers retaining the SAP, as well as the arrangement of the
containers. Thus, a core may be designed to attain optimized performance characteristics by
ng the size of the pocket and/or the concentration of SAP within that pocket.
In large diamond shaped containers or pockets 514 of absorbent particles
aggregate 522 are present in a region anatomically aligned with the point of insult. The
ners then gradually reduce in size toward the sides and front and rear margins or edges
of the core 510. There are three distinct regions of containers. In the crotch region "A", large
diamond shaped pockets are provided. Adjacent and surrounding the crotch region is an
intermediate region "B" of pockets of smaller size than those in the crotch region (A).
Among other things, the smaller pockets of this intermediate region (B) present breaks in the
potential fluid flow around the SAP aggregates and along ing lines. As described
previously, the presentation of such barriers to direct escape of fluid flow h the side
margins prevents leakage and promote utilization of the SAP aggregates. Finally, a third
region "C" of pockets is present near each of the end edges of the core 510 populated by even
smaller sized pockets of SAP aggregates.
illustrates a second exemplary arrangements of SAP aggregates 522 and
pockets 514. In this example, small, d shaped s 522 are disposed in the region
anatomically aligned with the point of fluid insults. The pockets then lly increase in
size in regions disposed toward the sides and front and rear edges of the core. The two
arrangements (in FIGS. 1A and 1B) provide alternative ways of uring the expected flow
gradient and as well, handling of the liquid insults. The absorbent composite and arrangement
of pockets in may provide for a center region with a larger capacity initially, but
which, over time, will redistribute liquid in its void volume, or from subsequent liquid insults,
to smaller adjacent pockets or cells. With the pattern of , the center region may be
equipped with smaller capacity lly, which will cause the liquid to travel to larger cells. It
may also generate a surface topography that prevents leakage from the sides and ends of the
diaper, z'.e., “dams” will be created that intercept and absorb surface flow.
Although the amount of SAP applied on a core by weight is of a capacity that is
tically sufficient to achieve a certain retention , Applicants found through
mental observations and then, calculations, that the SAP needed more volume in the
pockets. Applicants’ teabag volume calculations, which are reproduced under Tables A and
B below, suggest that there is insufficient volume in the pockets, tively, to allow
the SAP to fully swell, hold and contain the target 750g of liquid. There is insufficient void
space within the core to accommodate the excess volume ed by the swollen SAP
population. Without more expansion room, the absorbent capacity of the SAP was reduced.
The teabag calculations suggest that a diamond shaped pocket having a side
dimension of 23.5mm has a maximum al volume of about 2.5cm3 . This is supported by
testing that further suggests that a 23.5 x 23.5mm bag containing 0.25g of SAP absorbed
around 2.5-3.0g of saline solution. The core has 84 pockets resulting in a total internal
volume of only 210cm3, which is less than a third of the volume ed to hold 750g
(~746crn3) of fluid.
2014/045027
Table A. Quick Calculation of Pocket Volume for Pocket Designs
For Adult Product mm 23.55 75 100
—-mm 23.55 75 100
mm3 2488 2977 23814 80371 190510
—_cm 2.49 23.81 80.37 190.51
cm2 480 480 480
—_mm2 48000 48000 48000 48000 48000
—_---—_E
cm 214 643 762
ion of 750_!
Table B.
For Bab Diaer
—-—--—
—.-mm3 2977 23814 80371 190510
—_cm3 2.98 23.81 80.37 190.51
cm2 400
—_mm2 4000 4000 4000 4000
cm3 191
In one aspect, the present disclosure presents different approaches to solving the
above-illustrated capacity issues without compromising certain advantageous features of the
core design. For example, various embodiments are bed or contemplated that employ
diamond-shaped pockets in a core composite configuration but with the means or lity
to increase void volume or capacity during use events. The pocket configuration is
substantially defined by two material layers and how these two layers are secured to one
another and/or the aggregate of absorbent particles contained in the pocket. It is this pocket
ration that determine the volume of the pocket and r it can odate SAP
well. In certain embodiments, the pocket configuration is not fixed but dynamic. A means or
mechanism is provided for altering the pocket configuration so as accommodate SAP swell,
particularly when the collective swell volume of the SAP aggregate nears or exceeds the
fixed initial volume of the pocket. In some embodiments, the pocket configuration is altered
(e.g., responsive to SAP swell (pressure or liquid contact) to increase pocket volume or
capacity and/or to allow escape of liquid or SAP from the pocket.
In further embodiments, such pockets may be strategically positioned in or around
certain areas of the core to effect desired fluid flow and core absorption characteristics. In yet
further embodiments, the absorbent composite may be contained or encapsulated in a single
or a small number of pockets.
Multiple Layers of Core Material
[0070] In this embodiment, the absorbent core composite features a multi-layer core
construction. By increasing the number of core layers and thus, the z-dimension of the core,
the number of pockets in the absorbent core is sed. See e.g., and FIGS 6A-6C.
As a result, the total void space ble in the product is also increased (multiplied)
(assuming total SAP content remains the same but SAP amount per pocket is reduced).
FIGS. 6A-6C provides examples of multi-layered absorbent core composites 610a, 610b,
610c. The configurations for the latter two composites 610b, 610c position and favor
additional core layers centrally to coincide with target insult regions, for example.
In an alternative construction, a wider core sheet is provided and then folded to
produce the multiple core layers. Consequently, the total void space available in the t
is also increased (multiplied). Core layers can be the full length of the absorbent core or any
partial length of the absorbent core and can be stacked in any configuration ing
pping partial s of core.
Increase Pocket Size Dimension
[0073] In further embodiments, the core pocket dimensions are evaluated and manipulated to
achieve increased void space. The thrust of these core pocket designs is based on the premise
that a larger pocket provides greater void space. Generally, the volume of available void
space ses exponentially as the side length of the pocket is increased. With this
modification, a higher total ty per core may be ed without increasing the l
core size or the number of layers. Thus, in respect to the pocket configuration of FIGS. 2,
larger diamond shaped pockets are used, which also reduces the number of cells pockets
overall.
Wider Core Sheet Folded to Multiple Core Layers.
Referring to FIGS. 7A-7B in one embodiment, a wide core composite 710 can be
made () and then folded (), along one or more folding lines FF running
parallel to lateral side edges 720 of the composite to reduce the width of the total core
composite to a narrower width. Total void space is increased, as in other designs ing
total SAP content is the same but SAP amount per pocket is reduced). er, the two
folded portions may provide a contiguous top layer 722 to the composite. Notably, in such
case the base layer effectively encapsulates the composite and functions as both a core layer
and a base layer. Alternatively, in a r embodiment, a longer core is folded along one or
more folding lines parallel with the udinal front and rear edges of the core to reduce the
length of the core to a desired length.
In a method for producing a suitable folded core sheet, SAP free lanes may be
provided on the sheet of the nonwoven base layer as the sheet is conveyed. For example, SAP
is selectively deposited on the substrate along three longitudinally-extending lanes. Adhesive
d on the sheet and/or the SAP may be used to secure the SAP in place. Alternatively, a
cover layer may be applied over the SAP. The three SAP lanes are mutually spaced apart by
way oftwo SAP-free lanes, which extend in el with the SAP lanes. Downstream in the
manufacturing process, perhaps after a cover layer is provided over the SAP, the absorbent
composite may be readily folded laterally along a natural fold line extending through the
SAP-free lanes (where the composite is thinner). Before g, the base and cover non-
woven layers may also be bonded along the SAP-free lanes. Notably, for a composite
configuration such as that depicted in the base layer may function both as the base
layer and the top cover for the resultant absorbent core composite.
Extendible 0r Elongatable Substrates
[0078] In some embodiments, structural mechanisms are employed which, when triggered,
expand or extend the dimension of one of the layered components of the core composite or
more preferably, of the . With the extension of the substrate, the pocket volume is
increased, primarily in the Z-direction (vertical direction). FIGS. 3 and 5 illustrate another
absorbent composite (320, 520) having at least one elongatable substrate, preferably as a
nonwoven cover layer. The surface of the en layer is equipped with folds, flaps,
pleats, grooves, or other temporary surface breaks or ation formed during manufacture
of the composite and which disturb the ise flat surface. Rather than being flat or
smooth, the surface is riffled or corrugated. ed in plan view, the surface is not
continuous but exhibit lines or breaks (creped, riffled or corrugated) due to folds, protrusions,
grooves or depression. The surface may be hed, however, to smooth out the surface and
remove these temporary deformations or tinuities. In doing so, the surface area is
increased (i.e., a surface dimension is elongated or extended). Accordingly, in one respect,
the riffles or corrugations are said to represent reserved area or elongation of the surface. For
t purposes of description, the terms creped, riffling, or corrugations are used to
interchangeably to mean the appearance and condition of a surface as described above,
including having the capacity to smoothen, te, or extend to increase a surface area
dimension.
The riffles or corrugations may extend in either the machine direction or cross
direction, but preferably, in the machine direction due to ease of assembly. As the SAP
swells, it applies pressure on the nonwoven layer placing it in tension. The ing lateral
forces causes the surface discontinuities to unfold or smooth out, as the en layer
extends laterally. In this way, the volume of the pocket expands to accommodate the swell of
the SAP.
[0080] In FIGS. 3A and 3B, an absorbent core pocket P is shown having an elongatable
substrate in the form of a riffled or corrugated non-woven cover layer A. shows the
pocket P both in a pre-activated state (left side of ) and then in an activated or
expanded state (right side of ) terized by SAP swell. The composite includes a
base non-woven layer or ate B, the riffled or corrugated cover layer or substrate A, and
SAP aggregates 335 situated therebetween. The surface of the cover layer provides
corrugations 330 under which the SAP is ed. The total SAP amount in the pocket may
be in the range of 50gsm to . Defined by a series of peaks and trough, the
corrugations 330 may be fine and closely packed, or may be larger and provide deeper
troughs or valleys. The corrugations 330 may be well defined such that the bottom of the
troughs are close to the base substrate B, such as shown in . In this configuration, the
corrugations 330 tend to compartmentalize SAP 335 into mini-pockets. In other
configurations, the bottom troughs are spaced further from the base substrate and the SAP is
largely d below the cover layer.
As taught herein, bonding of the base nonwoven layer B and the cover layer
nonwoven A can form pocket patterns such as the diamond pocket pattern 340 (with
intermitted or spaced apart bond sites) on a sheet S of the absorbent composite 320 shown in
. The ter of the pocket forms a flat bonded area 342 as shown in . A
generally flat perimeter about the pocket P is maintained during expansion of the pocket P as
shown in the expanded state of the pocket in . Thus, the horizontal or lateral length
WO 02934
of the pocket P in does not actually extend because the cover layer A is fixed at the
bonded area 342. Extension of the cover layer A is instead generally accommodated by
expansion of the pocket P in the z-direction (depth).
The corrugations 335 in the non-woven structure of the cover layer may be pulled or
tensioned to elongate the surface dimension. When triggered by expanding or swelling SAP
aggregate, the pocket transforms from a rest or pre-activated ration to an activated or
expanded ration. This is rated in the right portion of . In the activated
configuration, the nonwoven surface has expanded or elongated such that the pocket volume
that it defines, at least partially, has increased to accommodate the collective swell volume of
the aggregate of SAP particles. l or preferred tion (extended length/original
length) is greater than about 1.2. Notably, the base nonwoven substrate B remains relatively
flat in this embodiment.
In exemplary embodiments of a disposable absorbent garment 310, as shown in , the s P of absorbent composite 320 are encased n a backsheet 360 and a
topsheet 350. The backsheet 360 and topsheet 350 maybe bonded or otherwise secured, but
their placement and configuration are such that these layers do not ct elongation of the
riffled substrate and expansion of the pockets P. Specifically, the topsheet is provided with
sufficient play and/or flexibility to readily accommodate the elongation and expansion. In
some applications, the et and/or eet is bonded to the absorbent core composite
throughout, e. g., employing the bonding patterns discussed above to form the pockets and
also bond the topsheet and backsheet. Such a bonding pattern may restrict some elongation of
the riffled substrate. In other applications, the topsheet and\or backsheet is bonded only at the
periphery. This bonding que would prove less restrictive on the lateral extension of the
riffled substrate. In one preferred embodiment, the topsheet is bonded only at the ery
and along one longitudinally-extending center line. In further embodiments, an ADL layer is
oned between the topsheet and the core.
In r preferred absorbent structure as first shown in FIGS. 3C and 3D, the
pocket P includes a top substrate A, a bottom substrate C, and a material layer B
intermediate the top substrate and bottom substrate. Substrates A and C are preferably non-
woven layers that are riffied or corrugated prior to absorbent core composite assembly. As
shown, the surfaces of substrates A and C exhibit riffles or corrugations 330 and a population
of SAP material 335 is provided in each of the pocket spaces above and below the
intermediate layer B. In the pre-activated mode, the dry SAP 335 settle close together
adjacent the intermediate layer B, asserting minimal pressure on substrates A and C. The
pocket P remains in a somewhat shallow or sed mode, ting minimal height (zdirection
) and riffled surfaces. illustrates the pocket P and the SAP 335 contained
therein in an active or nearly saturated mode. The space beneath substrates A and C now
contain SAP of larger sizes. The SAP materials have absorbed liquid to near volumetric
capacity, thereby expanding mostly in the z-directions, which asserts pressure on substrates A
and C and forces the layers to lengthen along the MD or X-direction. As a result, more void
space is d to accommodate the expanding SAP constituency.
The intermediate layer B may also be provided as an elongatable substrate in further
designs. In preferred embodiments, substrate B is an ADL-like structure, z'.e., bulky and
capable of distributing fluid. It is normally preferred, however, that one nonwoven layer of
the ite is not elongatable. Such a fixed-length nonwoven layer is required for
absorbent core ite processing and handling. Otherwise, the core composite would
stretch as it is being made rather than maintain the reserved length until product use. So, for
a preferred two-layer composite, only one layer is corrugated. In a preferred three-layer
composite, two of the layers are typically table while the middle or intermediate layer
is not elongatable.
In further embodiments, the intermediate layer B is a breakable substrate and more
specifically, breakable upon water contact. The intermediate layer B may be ed by a
tissue layer, for example. As the pocket P takes in liquid and the SAP expands, the wetted
tissue layer B breaks apart to allow SAP expansion to and from either top or bottom pocket
compartments. The direction of SAP ion (or ion) may be governed by physical
restriction or pressure applied to components of the pocket, and/or the direction of liquid
intake and travel. In many instances, ally for pockets situated in or about the l
region of a diaper where insult is initially expected, SAP ately beneath the cover layer
A will begin to swell first and exert pressure downward to adjacent SAP les and then
the intermediate tissue layer B.
In addition to improving the capacity of the core pockets, the riffled core design
produces a few side benefits. Due to the depth of the corrugations, the riffled nonwoven laver
necessarily provides more nonwoven material than a flat layer. The non-woven material is
absorbent and thus, the additional nonwoven material and nonwoven surface area increases
the absorbency of the composite. The increased thickness of the nonwoven surface due to the
depth of the corrugations also improves the absorption rate of the composite. The nonwoven
surface functions as temporary storage for liquid much like a l acquisition and
distribution layer.
As compared to a plain core surface, the appearance of the corrugated structure,
perhaps in ation with a desirable pocket pattern, may look aesthetically pleasing and
technologically advanced (market appeal). It may also look more comfortable, which,
indeed, is a side benefit of the design. The ated core structure should be less stiff and
generally softer than traditional core designs. A diaper (or other articles) employing the
absorbent core is, therefore, more comfortable to a user than a ional diaper.
In preferred embodiments, the riffled nonwoven layer is configured such that the core
is stretchable in the CD (cross) direction. See . This means the corrugations and the
troughs d by the corrugations extend longitudinally or in the machine direction. This
allows the pockets to continue ing until the stretch limit of the nonwoven is reached,
thereby zing the void volume within the core. In this regard, the cell pattern is MD-
biased (machine direction biased). FIGS. 2C-2D illustrate workable or suitable cell patterns
240, 240' diamond shaped pockets P or rectangular shaped pockets P'.
, using
illustrates another diamond shaped bonding n 240" using intermittent bond points Tl,
T2. An onal benefit of CD elongatable pockets is that when the diaper is fitted to the
user, hing of the diaper around the body will cause some of the pockets to be pre-
ted and elongated.
It should be noted that pockets or cells having expandable properties as described
above and in further embodiments may be strategically positioned in and around ent
regions of the core composite. In some applications, such pockets may be ed in the
central regions so as to receive directly and accommodate intake. In other applications, the
core composite may be configured to readily and rapidly receive intake at the central regions
and direct flow to the side regions. In such designs or ration (but not all), it may be
advantageous to locate higher volume s in the side regions.
[0091] illustrates various methods or techniques for riffling or corrugating a sheet of
the ate A or C (forming or treating the surface so as to exhibit corrugations or riffles
thereon). also illustrates equipment that may be suitable for use in riffling the sheet.
Referring to the illustration provided above label (a) in a nonwoven sheet 400 is
moved, under tension, past a comb 480 with hard, protruding fingers 482 that sharply
engage and temporarily deforms the top surface of the sheet 400. This creates corrugations
430 or elongated riffles (scratching) on processed sheet 402. The dimension of the
corrugations 430 will determined by the configuration of the fingers 482, as well as the basis
weight and/or stiffness of the non-woven material. A thinner or more flexible nonwoven will
form finer riffles or corrugations. Thicker non-woven can e deeper corrugations and, as
a result, greater elongation. Elongation may also be increased with the frequency or pitch of
the corrugations. Preferably, permanent deformation (gouging, g, breaking, etc.) is
avoided or at least minimizes, so as not to compromise the structural ity of the material.
The nonwoven sheet may be riffled before application and prior to integration in a system for
making the absorbent core, or, in a system just upstream of SAP deposition. A roll of the
riffled en may initially be stored on and red via a spool. It is conceivable,
however, that in further embodiments, a nonwoven ate is riffled in place, while it is
serving as barrier to a population of SAP units.
According to r process option, illustrated and labeled as (b) in the
ate 400 is placed into a engagement with a grooved roll 484 (or meshed slotted roll).
The hard surface profile of the roll 484 impresses the substrate with ary s into
the substrate 400. The substrate 400 may be moved horizontally toward the grooved roll 484,
as shown in and into engagement with the hard profiled surface of the roll 484.
Tension applied generally downward from and perhaps, generally perpendicularly to the
horizontal direction causes the sheet 400 to turn about the grooved surface, whereby the
outside e of the roll 484 penetrates the substrate's surface. The amount of tension
applied on the substrate, the angle at which the tension is applied on the moving substrate
(downstream of the roller), the pitch and depth of the grooved roll's surface, and the
ions and physical properties of the substrate, among other things, may be adjusted to
achieved the desired riffled or corrugated substrate (with minimal or no permanent
deformation or tearing) for use in an absorbent core composite, according to the t
disclosure. In accordance with yet r process option, illustrated and labeled as (c) in
a pair of male and female grooved rolls 486 replaces the single roll to etch the passing
substrate. As shown, the substrate 400 is passed h the interface of the two rolls 486 to
produce the riffled or corrugated sheet 402.
In the preferred embodiments, only one outside surface of the substrate is corrugated
and employed in the absorbent core. It is conceivable, however, that the etching process can
readily etch or scratch both surfaces of the substrate. Strategic use and placement of
substrates having corrugations on both sides (e.g., in and about target areas of insult) may
change the fluid ng mance in those areas. Corrugations on both sides may
provide additional storage capacity and\or enhance ADL-type fluid handling performance. It
may provide a higher density of corrugations, if desired. Noting that a topsheet and ADL
layer is typically added above the substrate, placement of the corrugations on the outside
surface may not necessarily sacrifice comfort.
The simplified illustrations of FIGS. 5A and 5B depict r absorbent core
composite 520 having a means for accommodating SAP swell during use. As with the
absorbent core ite 320 of FIGS. 3A-3D, the absorbent composite 520 utilizes an
elongatable substrate as a top nonwoven layer A over the SAP aggregate 535. The top
nonwoven layer A may be activated by SAP swell to se the volume of the pocket or
cell P and accommodate the additional SAP volume. In the specific configuration illustrated,
the absorbent composite 520 has the top elongatable nonwoven layer A, a base nonwoven
layer B, and SAP aggregates 535 situated therebetween. Referring to , bond sites
542 securing the top layer A to the base layer B mark the boundaries between SAP
aggregates 535 and partly define individual pockets or cells P that contain SAP aggregates
535 thereunder. The SAP aggregates 535 and the pockets P are therefore spaced apart fiom
adjacent SAP aggregates and pockets.
In this embodiment, the top layer A is provided with two pleats 530 or sets of double
folds. The pleats 530 may be formed on the source sheet of nonwoven as the sheet is being
conveyed in-line toward a web of the base nonwoven-SAP after SAP deposition. A pleat
may be formed by applying a pair of opposite-facing folds on the moving sheet, as generally
known in the art. In the illustrated ment, a pair of pleats 530 is provided for each
pocket P and located to achieve the desired pocket profile when the SAP 535 swells to fill the
pocket P. The folds or pleats 530 are sized to facilitate transition of the pocket P from a pre-
active or thinner state to activated and full step (and other states of swell in between). It is
desirable to maintain a smooth top surface and profile so as not to compromise user comfort
and risk pinching of the skin by the folds or edges. In this respect, the number and size of
folds and pleats may be coordinated with target swell capacity and transition performance to
e optimal results. After applying the elongatable substrate over the SAP aggregates,
the resultant composite may be passed into engagement with one or more embossing rolls to
apply the d bonding or pocket pattern.
shows the absorbent composite 520 in an a state of full SAP swell and in an
activated state. For each pocket P, folds or pleats are no longer evident (completely
unfolded), revealing instead, a somewhat rounded top e rather than surface
tinuities marked by sharp edges or peaks. In further embodiments, pockets with
elongatable substrates (such as those illustrated in or FIGS. 3A-3D) may be
employed in conjunction with other means for pocket expansion or ry ge. For
example, the pocket configuration of FIGS. 3 or 5 may be ed with the ble bond
pattern of . The fold pattern and the bond point sizing may be coordinated, for
example, so that during use and upon liquid migration into the , pressure due to SAP
swell acts to elongate the top substrate first. When the volume of the pocket cannot be
odated by pocket volume se, certain of the bond points may be designed to
break. In other designs, the absorbent core design may call for some amount of bond
breakage to occur simultaneous with or preceding the elongation of the elongatable substrate.
Programmed Bond Breakage
In further embodiments, the core construction is provided with pockets having
dynamic ries or capacities and thus, mechanisms for increasing void space.
Specifically, isms are ished to trigger and allow for the pocket boundaries or
break so as to relax the restraint on contained SAP material. Specifically, the bonds between
the pockets are made to break or unzip so that the SAP can ue to swell beyond the
maximum volume of the pocket. In one embodiment, discontinuities in the bond lines are
provided, whereby strength of the remaining bonding strips or points are designed to be less
than SAP swelling pressure.
In an alternative embodiment, the layers may be secured by ultrasonic bond sites,
which may be “tuned” to a certain minimum threshold strength that may be overcome by
SAP swell may overcome. Furthermore, the use of adhesive bonds, perhaps in conjunction
with ultrasonic bonding, may be employed and “tuned” to provide a desired bond strength by
changing and manipulating the bonding pattern. For example, lower bond strength may be
achieved by smaller bond sites and higher bond strength may be achieved by larger or longer
bond sites. In other embodiments, the ultrasonic bonding may serve as the stronger or
permanent (or ) bonds, whereas adhesive bond sites serve as breakable bonds or
barriers. Different manners of SAP swell and pocket volume expansion may be achieved
h such manipulation and bond programming.
In one application, a heated calendar roll (or ultrasonic bonding) is employed
to heat, melt, and fuse the nonwoven layers at bond points. Generally, bond points below 1
mm wide break during normal use and incident of 75% (of swell capacity) SAP swell in
pockets. Bond points larger than lmm er larger were observed to not break or break
later. illustrates a pocket pattern 240" and configuration for an ent composite
according to an embodiment employing breakable bonds, ing to the disclosure. The
absorbent composite utilizes a diamond embossing n 240" with intermittent (spaced
apart) bond points Tl ,T2 forming diamond shaped pocket. In this pattern, the bond points T2
located at intersections of bonding directional lines are sized to be permanent bonds while
most, if not all, of the bond points Tl between the intersections are breakable. The bond
points T2 at the ections have a diameter of about 1.5mm while intermediate bond
points Tl have a er of about 1.0mm (providing a bond area about half the size of the
bond area at the intersections). Many of these smaller bond points T1 are expected to breach
at high SAP swell states (of the adjacent pockets).
In another embodiment, water sensitive ve may be used in the
lamination. The adhesive s when contacted with water and wetted, and is overcome
by increasing swell pressure. Adhesives used to form a water soluble bond may employ as
components, polymers that make water soluble resins, including ethylene vinyl alcohol
and/or nyl alcohol.
In yet another embodiment, hotmelt bonding may be employed (e.g.,
thermoplastic particle) to serve as the programmable, breakable bond site. In this
mechanism, the hotmelt/SAP combination serves as the adhesive during manufacture and
passive use of the absorbent article. When wetted, the SAP swells and weakens before
breaking. As with the other proposed bonding site mechanisms, the hotmelt/SAP bond sites
may be used in conjunction with one or more of the other bonding mechanism to achieve the
desired breaking and pocket volume expansion effect.
Substrate Control
] In some embodiments, volume expansion is effected by employing a dynamic
composite layer or component. In one technique, one layer is provided by a relatively weak
material that is overcome by the aggregate of SAP les swelling beyond the pocket
volume. For example, an intermediate layer, such as substrate B in , may be made of
tissue material that opens or is otherwise compromise by the swelling SAP aggregate, thereby
expanding the void capacity. Suitable candidates for the material include dry-crepe tissue,
which elongates when wetted. A low wet strength tissue (e.g., low basis weight tissue) may
also be selected, which weakens when wetted and is readily overcome (breaks) by SAP swell.
A third material option is a slitted substrate. A fourth option is a al that has been
weakened or ated so as to be able to open up by the force exerted by the ng SAP.
In these embodiments the swollen SAP may no longer be fully contained by the material
ents of the core. Provision for the storage and containment of this swollen SAP would
need to be made within other elements of the absorbent article. In any case, upon contact with
liquid or with increasing re asserted by a collectively ng aggregate of SAP, the
layer opens to communicate the SAP aggregate beyond the initial fixed volume of the pocket
A "tissue" is generally a (paper) cellulose-based nonwoven as opposed to a
synthetic nonwoven. Preferably, the tissue is provided as a bottom or base layer of the
absorbent composite, if it is intended to function as a breakable substrate. As such, it may be
y supported by a backsheet beneath it for contain liquid. In red designs, it would
be advantageous to size and\or secure the backsheet and tissue layers so as leave expansion
(containment) space beneath the tissue layer. For example, the backsheet may not be
completely or tightly bonded to the core. Alternatively, a bulky nonwoven layer may be
employed to provide the thicker profile.
[00106] r Core Composite Design Considerations
In several applications wherein SAP is at least partly contained or
immobilized by a fibrous network or other matrix, a procedure may be ed to facilitate
the deposition of the SAP particles within the matrix. In the embodiment n a bulky
nonwoven is used as a substrate to stabilize the SAP les, the web carrying the SAP on
the substrate may be vibrated or shaken to impart energy on the supported SAP particles.
The added energy enhances the matrix’ ability to capture and embed individual particles
therein. In another embodiment, energy is imparted on the SAP particles by applying a
vacuum to the outside of the substrate, which draws the particles toward and into the
substrate. In either case, suitable equipment may be positioned immediately ream of
where SAP particles is deposited on the web of substrate.
] In another embodiment, SAP of different tion ties, z'.e.,
absorbency under load (AUL), absorption rate or aggregate flow properties, z'.e., liquid
bility, may be deposited in specific MD-stripes. For example, a stripe of
approximately the same width as the length of a diaper target zone is deposited as a central
zone with two stripes comprising another SAP type adjacent and abutting both sides of the
first stripe. The SAP arrangement will be utilized in a CD-diaper forming process. That is, the
t is formed with the longitudinal direction of the product oriented in the transverse or
CD direction in the diaper converting line.
FIGS. 8A-C depict three core composition design patterns (810a, 810b, 810C)
in which ent grades or types of SAP material are positioned strategically to achieve
desired absorption characteristics. In a que that may be described as cross-directional
(CD) profiling, certain centralized target areas or zones 822 of the core are provided with
slow absorbing SAP with high absorption oad (AUL) and high permeability. In
contrast, the outside areas or zones 824 are provided with slow absorbing SAP with low AUL
and low permeability. The effect is that the initial intake in the central region 824 is only
partially absorbed by the slow absorbing SAP with excess fluid flow being buted to the
outside regions, where it is absorbed rapidly and thus, stored. Higher mance is
achieved primarily because the initial liquid insults are aged to spread and flow to the
ends of the diaper due to the slower absorption rate or higher permeability of the first SAP
which allows the liquid to flow through the target zone and into the end zones. For
subsequent intakes, the central region provides yet remaining capacity to receive some or all
of the additional fluid.
[001 10] SAP Permeability
[00111] For present es, a SAP gel bed permeability greater than about 40
Darcys is considered a high permeability SAP. A permeability less than about 5 Darcys is
considered a low bility SAP. In this respect, gel bed permeability is measured under a
0.3 psi load using 0.9 percent saline on on a 40-50 mesh particle size cut by the method
described in Buchholz, FL. and Graham, A.T., "Modern Superabsorbent Polymer
Technology," John Wiley & Sons (1998). page 161. As known to one skilled in the art, the
term "Darcy" is a CGS unit of permeability. One Darcy is the permeability of a solid through
which one cubic centimeter of fluid, having a Viscosity of one centipoise, will flow in one
second through a section one centimeter thick and one square centimeter in cross-section, if
the pressure difference n the two sides of the solid is one atmosphere. It turns out that
permeability has the same units as area; since there is no SI unit of permeability, square
meters are used. One Darcy is equal to about 2><10'12m2 or about 2><10'8 cmz.
[001 12] Absorbency Rates
Generally, most commercial SAPs have a vortex time ranging from 40 — 90
seconds. A vortex time of less than 40 would be considered a fast or high absorption rate SAP
for present purposes. A vortex time of greater than 100 would be considered slow, again for
present purposes. As understood by those skilled in the art, the Vortex Time Test measures
the amount of time in seconds required for a predetermined mass of an absorbent polymer to
close a vortex created by stirring 50 milliliters of 0.9 percent by weight sodium chloride
solution at 600 revolutions per minute on a magnetic stir plate. The time it takes for the
vortex to close is an indication of the free swell absorbing rate of the absorbent r.
[001 14] AUL bency Under Load):
For t purposes, an absorbency of greater than about 15 g/g at a load of
0.09 psi would be considered high AUL. As understood by those skilled in the art, the test
measures a superabsorbent’s ability to absorb 0.9% saline solution against a defined pressure.
Test procedures entail g a bsorbent a plastic cylinder that has a screen fabric as a
bottom. A weight or load giving the desired pressure is put on top. The cylinder arrangement
is then placed on a liquid . The bsorbent is soaked for one hour, and the
absorption capacity is determined in g/g. See European standard EDANA ERT 442 —
GraVimetric Determination of Absorption under Pressure or Absorbency Under Load. See
also the AUL-test found in column 12 in United States Patent No. 542.
rates, in simplified n, a system 1400 and process by which
a sheet of an absorbent composite may be made according to the disclosure. In one respect,
the system previously bed of may be modified to incorporate elements of the
system of to make an absorbent composite exhibiting SAP variations in cross
machine direction. As described before, a web or sheet of a first fabric or substrate 1425 is
preferably conveyed to present a planar surface. The substrate 1425 is passed beneath a SAP
dispenser 1480 with means for segregating different types of SAP 1435 and depositing SAP
types through apertures gically positioned relative to the moving substrate 1425. In the
rated embodiment, the dispensing apertures are positioned to deposit SAP at spaced
apart points, which create laterally spaced apart lanes 1437 of SAP on the moving substrate
1425. Furthermore, SAP-free lanes 1439 are provided between the SAP lanes 1437.
Subsequent to SAP deposition, the second fabric 1455 is applied over the
SAP-lanes creating the desired laminate. As required, the resultant laminate may be passed
to a bonding area 1442 to apply the desired bonding pattern 1440 on the laminate. In an
absorbent composite taken from the laminate, the SAP-free lanes between strips of SAP can
act as channels for y directing liquid received therein.
SAP-free lanes may also be formed by providing folds in the substrate 1425
before the sheet is passed to the SAP dispenser 1480. Referring to , the folds may be
located where the SAP-free lanes shown. In this ment, the SAP dispenser is selected
and\or operated to apply SAP generally uniformly across the substrate 1425, including over
the folds. Hotmelt adhesive is the applied over the SAP to secure it to the substrate.
fter, the folds may be opened (e.g., by a tenter device) to reveal the SAP-free lanes. In
a filrther embodiment of the absorbent composite, the folds are maintained in the finished
absorbent core composite rather than opened. In this way, the substrate 1425 functions as an
table substrate that may be activated by SAP swell during use.
Additionally, another feature that can be added in the construction described
above is the addition of a small percentage of ion-exchange particles 907 to a second SAP
mixture deposited in target areas, and more specifically, the end zones (outside zones 924)
away from the points of insult. It has been found that the ionic strength of the urine as it
passes through a bed of SAP materials (S) increases because of the SAP absorbing its water
content. This is shown in the m of , which illustrates the receipt area 922 of an
absorbent core 910 for insult and the typical travel (see directional arrows) of liquid in the
core 910 after initial receipt in central zone 922. The perimeter of core 910 is defined by a
pair of end edges EE and a pair of side edges SE. The primary insult target 922 of the core
910 (where liquids are typically received by the core 910) is generally in and about the center
of this defined perimeter. Directional arrows in indicate the general e or
spread of the liquid after receipt.
[00120] The graph 901 of is drawn to correspond with the expanse of the core
910 in . The graph 901 rates the change in the liquids ionic strength as it travels
along the core 910 and the effect of this change on SAP ent capacity. lly, the
absorbent capacity of SAP is reduced as the ionic strength of the liquid being absorbed
ses. See graph 903 of . Because SAP swelling decreases with the se in
ionic strength of liquid being absorbed, SAP (S) that is furthest away from the liquid source
and which contacts liquid having higher ionic strength, will have lower swelling properties.
The graph 902 of illustrates the effect that the introduction of ion-
exchange les has on the SAP absorbent capacity of the same areas of the core 910. The
introduction of ion exchange particles along the path of the liquid, ing in these SAP
areas (S) (specifically, the end zones 924) will lower the ionic strength of the liquid being
absorbed there, thereby maintaining the absorption capacity of the SAP. Ion-exchange
particles 907 in the fluid path restores capacity of the SAP by ng the ionic strength of
the urine reaching the ends of the core 910. So for example, a cation ion exchange resin can
remove or lower the concentration of multivalent s like Ca++ and Mg++ present in
urine, hence effectively lowering the ionic strength of the urine. A typical cation exchange
resin is Dow Amberlite 200C Na, used at between 1-10% of SAP content.
Accordingly, higher performance will be achieved with this uction
since more liquid can be absorbed by the SAP (S) at the end zones (924).
In still another embodiment, narrow lanes that are relatively SAP-free are
formed for the purpose of creating stripes used in producing diaper width strips that are
bonded and sealed at the slit lines. Because several diaper widths strips can be cut from the
material envisioned by this process, producing these narrower strips with sealed edges have
several advantages. These include minimizing potential SAP loss during subsequent
handling. This also obviates the need for a separate core wrap when assembled into a diaper.
The SAP-free lanes can also y serve to accommodate bond lines in
further processing. Additionally, these lanes can provide fold lines required of the composite
design.
In r embodiment, a liquid phase/spray application of hotmelt adhesive is
utilized to provide yet r form of binder or matrix to stabilize and lly immobilize
SAP particles. In an extrusion process, hotmelt adhesive is forced through small holes which,
in combination with air attenuation, produces elongated polymer strands or fiber. Deposited
on the substrate, the elongated polymer s establish a fibrous network e of g
the SAP particles.
[00126] The fied illustration of provides a system 1500 that may be
employed to apply the fibrous network. As before, a SAP dispenser 1580 may be used to
deposit SAP 1535 on a moving fabric or substrate 1525. In the illustrated embodiment, SAP
1535 is applied uniformly across the planar surface of the ate 1525 as it passes beneath
the dispenser 1580. The SAP 1535 may be held in place, thereafter, by a variety of
mechanisms, including applying suction applied to the ide of the substrate 1525, as
discussed previously. Then, the substrate 1525 and SAP 1535 combination is passed beneath
a hotmelt fiber extruder 1586 that dispenses and applies hotmelt fibers 1539 over the SAP
1535 and substrate 1525. The resultant composition 1510 is shown in the inset of .
[00127] Nonwoven Design and Selection
To achieve core performance objectives, the various core composite
components may be d or specifically designed (individually or in combination). The
core performance ties of interest include absorption properties, ing rate and
capacity, permeability, rewet performance, and structural integrity.
[00129] The core composite typically includes a permeable top layer that receives
intake and then helps contain absorbent material within the core. In one design, a nonwoven
material may be selected that has an outside surface that is more open than the inside surface.
The more open surface serves to y receive SAP particles thereon, and in that respect,
binds and at least partially immobilizes the SAP particles. In contrast, the opposite surface is
relatively dense and ageously more impermeable. This surface acts to block the
penetration of SAP particles beyond the network of fibers presented at the more open surface.
While SAP particles, particularly the smaller ones, are received and slightly encapsulated by
the substrate, they are ted from passing through the substrate. As mentioned
previously, the substrate may be energized to facilitate receipt of the SAP particles by the
more open e.
The nonwoven described above is sometimes called a "bulky" nonwoven.
Reference may be made to ding '051 patent international application for filrther
description of suitable bulky non-woven al and selection. The “bulky” nonwoven
referred to herein is, and provides, an open, fibrous network or web of hydrophilic but non-
absorbent fibres. Further, as used herein, a bulky nonwovens is a fibrous web material
having a thickness of between IOOum and 10,000um (preferably 1,000um to m), basis
weight between 15g/m2 and 200g/m2 (preferably, between 20g/m2 and 80g/m2), and density
between 0.01 g/cc and 0.3 g/cc (preferably between 0.01— cc). Moreover, the bulky
nonwoven will have an effective pore diameter between 300 um to 2000um.
In further applications, it may be advantageous to employ consolidated but
unbonded or lightly bonded en as one of the substrates. The unbonded surface may
serve well embedding and supporting the SAP particles. The outside may be bonded,
however, so as to maintain structural integrity and impermeability. In further applications,
the unbonded e may be bonded after application of SAP particles thereon by using
t or infrared heating. This procedure may be necessary or advantageous, as it s
structural integrity to the composite’s nonwoven layer. Although an already bonded
nonwoven layer may have been used, the bonding in place technique allows for the SAP
les to be bonded and supported also, in one bonding operation. By using hotmelt or IR
to bond the nonwoven (with SAP) after application of SAP, the nature of SAP ulation
and hence the ite integrity, swelling properties and fluid flow or permeability
characteristics can be varied and lled.
] In specific embodiments, suitable bulky/high loft materials contemplated for
use in the above suggested applications are a type of “through air bonded” nonwovens. The
nonwovens are made by taking a carded web or mat of fibers and using hot air to bond the
fibers at the points where the fibers intersect or join. The hot air “blowing” through the web
serves to keep the fibers separated to some extent and uncompacted. The resultant structure
is, therefore, fairly open but fixed by bonds formed n the intersecting fibers. (This is
different from the traditional process by which non-bulky, regular nonwovens are made,
wherein an unbonded mat of fibers is passed through heated bonding rolls that compact the
fibers and form a thin web of nonwoven, and leave an embossed bonding pattern). In an
exemplary method of cturing the absorbent composite, a web of carded, unbonded
WO 02934
fibers (e.g., PET fibers) is conveyed and SAP is deposited on the web. Hot air or other
suitable means is then used to bond the SAP and the non-woven in place.
Hotmelt ation Design and Selection
As described previously, in one embodiment, a liquid phase/spray application
of hotmelt adhesive is utilized to provide yet another form of binder or matrix to stabilize and
partially lize SAP particles. In an extrusion process, t adhesive is forced
through small holes which, in combination with air attenuation, produces elongated polymer
strands or fibers. Deposited on the ate, the elongated polymer strands establish a
fibrous k with capacity to hold the SAP particles.
In an alternate , powdered hotmelt adhesive particles can be mixed
with superabsorbent particles and the mixture of unbonded hotmelt particles and
superabsorbent particles is applied to the nonwoven substrate. Application of heat to the
composite will cause the hotmelt adhesive powder to melt and bind the SAP and en
substrate. The application of heat can be accomplished through IR (infra-red) radiation
methods, heated calendar rolls or other means.
The ion of hotmelt material and processes as a design element can
achieve particularly improved product performance. In filrther applications, the ratio of
hotmelt particles to bsorbent particles is selected to achieve an optimum e of dry
integrity and restraint on SAP swelling. The ratio of the number of SAP les to hotmelt
particles will determine for example, how many bonding points, contributed by the hotmelt
particles, per SAP particle are possible. The ratio is determined from the weight percentage,
particle size distribution and polymer density of each component. For example:
0 -300
article ratio HM to SAP: 46.79 27.06
103%
Here, optimum adhesive content is defined as one particle of hotmelt per
particle of SAP and uniform mixing is assumed. The ratios shown are for commercially
available SAP and hotmelt les. The chart of provides particle size distribution
for a SAP al SAP (W-112 from Nippon Shokubai). The hotmelt particles are
commercially available materials from Abifor and have the following particle size
distribution provided in . The t to SAP weight ratio can range from 1% - 30%
of SAP content, ably from 4% — 12%.
The selection of hotmelt material and processes as a design element can
achieve particularly improved product performance. In some applications, water sensitive
hotmelt particles may be employed as a mechanism for increasing void space (swell volume).
Specifically, a hotmelt is selected that is sensitive to wetting (e.g., an SAP based hotmelt) and
thus, to receipt of liquid intake in the absorbent core pockets. These hotmelt particles break
down as the SAP particles around it swell with liquid absorption. This relieves the SAP
particles from the hotmelt’s bind and allow the SAP to swell unrestricted. An example of a
water soluble hotmelt is the modified polyvinyl alcohol resin (Gohsenx L series, Nippon
Gohsei). An example of a water sensitive hotmelt is Hydrolock (HB Fuller).
SAP Selection and SAP Aggregate Constitution
As described previously, the pockets of SAP aggregate need not be uniformly
provided or distributed across the core composite. Variations in pocket size and shape,
pocket volume, SAP volume, SAP-pocket volume ratio, and SAP concentration may be
lated to achieve mance objectives. In addition to those design parameters, the
distributions or constituents of the pockets, including the SAP aggregate, may be varied as
design elements.
[00141] In various embodiments, absorbent composite design takes into account the
size and distribution of the SAP particles. As general guiding principles, the permeability of a
SAP ly ses ly with les sizes (large SAP particle sizes have highest
permeability). For example, doubling the particle size will double the permeability of the
SAP assembly. Further, the permeability of a SAP assembly decreases with loading or
swelling restraint (effect seen with small pockets). Finally, permeability ses with
increasing saturation (after initial 25% saturation).
In one ment, the SAP aggregate constitution may be selected to include
a certain mix of smaller particles that penetrate the surface of the nonwoven layer and larger
particles that generally remain above the nonwoven surface. The nonwoven surface may also
be prepared or preselected based at least partially on the d particle filtration effects. The
result is a layering of the SAP les at the interface of the non-woven and the SAP (see
e. g.. absorbent composite 1110 of ). Such ng and separation of SAP particles
can be utilized to change the fluid uptake behavior of the segregated layers formed. The layer
formed from the larger particles will have a higher permeability relative to the layer formed
from the smaller particles. Such an ement can encourage the lateral flow of liquid
during the insult resulting in more fluid bution and spreading. To aid the filtration
technique, the nonwoven may be energized during the manufacturing process to impart and
encourage particle tion in the SAP.
In methods of manufacturing the preferred composite, the multi-layer core
substrate may be pre-fabricated by a supplier according to specification. Suitable "through-
air bonded non-wovens" may be made in a single process by combing PP/PE/PET fibers into
a web and then bonding the web by blowing hot air h the non-woven. As a result,
thermal bonds form between the crossing fibers. As generally known in the art, multi-layer
structures may be made by g different layers of nonwoven on top of each. For
example, three combs may be provided to build up three different layers of nonwoven, each
layer having a different combination of fibers, density, and thickness. Preferably, a roll of the
prefabricated multi-layer substrate is ed onto a manufacturing line whereupon a SAP
mixture is deposited on the moving core ate.
[00144] In the alternative, the multi-layer core substrate may be made on-site and
further, on-line. For example, three te rolls or sheets of high loft ens maybe
delivered (e.g., unwound) and combined into a multi layer web. The layers may be bonded
by applying a layer of hotmelt adhesive between each layer of nonwoven (e.g., applied by
spray or slot hotmelt coater). Alternatively, the nonwoven layers may be point or line
bonded by applying heated engraved/pattemed calendar roll onto the web. An ultrasonic
bonding method may also be employed. In any case, thermal or ultrasonic bonding may be
performed before or after depositing SAP onto the layer core substrate.
To reduce cost and s complexity, each of the SAP intended for each
layer is joined with and delivered onto the multi-layer substrate simultaneous with the other
SAP tuents. SAP grades are selected having the desired particle sizes and ranges. The
arrangement of different density nonwovens will act to separate and place the SAP particles
in the appropriate layers. It is contemplated, however, that certain applications may require
separate and independent tion of the different SAP populations directly onto the
intended core ate layer. In one example, the smallest SAP les are applied directly
onto highest density layer, the medium size particles applied to the ediate layer, and
largest particles applied to the lowest (and top/bodyside) density layer. In a more specific
example, the bottom nonwoven layer is first conveyed and then deposited with the supply of
small SAP particles. Then, the intermediate layer is applied over the f1rstnonwoven layer
followed by deposition ofmedium size SAP particles ly onto the exposed surface of the
2014/045027
intermediate layer. The top nonwoven layer is then applied over the SAP-saturated
intermediate layer, followed by larger particle size SAP being deposited directly onto the top
nonwoven layer.
In certain embodiments, a disposable absorbent article incorporating the
absorbent core composite will include a topsheet and backsheet. The core composite is
sandwiched between the topsheet and backsheet, with the topsheet ing the bodyside
liner or cover. In fiarther embodiments, the bodyside al layer of the core composite
functions as the et, thereby eliminating the need for the topsheet.
] For purposes of this description, low, medium, and high density nonwovens
are nonwoven materials having a density of 0.01 to 0.03 g/cc, 0.03 to 0.08 g/cc, and 0.09 to
0.12 g/cc, respectively. The preferred thickness of the low, medium, and high density
nonwoven layers is 1.5mm to 5 mm, 0.6 to 3mm, and 0.15 to 0.6mm, respectively. The
specification s on the basis weight and density of the nonwoven, as shown in Table 1
below. Table 1 below may be referred to in selecting suitable low, medium, and high density
nonwovens to satisfy absorbent composite design requirements. er, red
nonwovens will be cially available multi-layer webs of different fiber denier and
density for each layer, typically using carding technology with multiple formers. An example
of such a le web would be a double or triple layer structure typically used as an ADL
(acquisition-distribution layer) available from Libeltex Nonwovens, Belgium, (Dry Web
TDL2, Slim Core TLl, TL4, TLS).
Table 1. Web Thickness (in microns) vs. Basis Weight and Density
Web Thickness (in microns) vs. Basis Weight and Density
3 0.012 0.02 0.05 0.06 0.073 0.032 0.093 0.1% .
1500 V
I ' ‘ i '
Weight
Basis
A typical core composite will be provided with SAP in the range of about 100
gsm to 500 gsm. Of this amount, about 5% to 75% may be in one single layer of the
absorbent composite. The t density layer may have as little as about 0.5% to 5% of the
total SAP amount. It should be noted that some SAP may not penetrate onto the nonwoven
layers at all, but sit on the outside surface. In exemplary two layer constructions, the average
size dimension of SAP les (z'.e. , width or diameter) targeted for a first or high y
layer (and which, will generally pass through a nonwoven layer above it) is 0-300 microns.
The second or lower density layer will contain larger sized particles, ing led
medium size and large size SAP particles typically in the 300-850 microns range. In a three
layer ite, the large SAP les, which are expected to not penetrate the intermediate
layer, will be retained in the top or lower density nonwoven layer and have an average size
dimension greater than 600 microns (in the 600-850 microns range), and the medium size
SAP particles will be in the range of 300 to 600 microns (in the intermediate density
nonwoven layer). Accordingly, the smaller size particles will be in the range of 0 to 300
microns (in the high density nonwoven layer).
provides, in elevated sectional view, an absorbent composite
1110 having a multi-layer configuration sed above. A high density en serves as
the base layer NW1 and is shown containing a representative population small SAP particles.
An intermediate layer NW2 is provided by a medium density nonwoven and contains a
representative population of medium size SAP particles S2. Finally, atop the intermediate
layer NW2, a low density, open nonwoven provides a top layer NW3, which, as incorporated
into a disposable absorbent particle is situated bodyside (closest of the composite's layers to
the user's skin) and likely adjacent a topsheet.
In some embodiments, the SAP particles penetrate well into the multi-layer
composite and may be bonded therein (e. g., by application of hotmelt particles, spray
hotmelt, etc.). No additional cover layers are required. In making the disposable absorbent
article, a topsheet is applied directly over the multi-layer composite. In other embodiments,
an additional nonwoven layer or even tissue is applied as a cover layer over the composite to
further secure the SAP. Alternatively, the additional nonwoven or tissue may be d all
the way around (enveloping) the multilayer composite construction. In r alternative
embodiment, hotmelt fibers is sprayed over the top surface of the multilayer construction
maintain the SAP in place.
It should be noted that particle size determination as alluded to above, and in
the ion of such particles in a corresponding design or method, is largely implemented
by equipment operated to se the SAP. In suitable applications, a sieve will be provided
with the appropriate screen or mesh. The screen or mesh will be c to the size of SAP
les being separated. Furthermore, the separation and\or mixing of SAP particles may be
partly or entirely performed in process, preceding to or in conjunction with SAP deposition,
or prior to the manufacturing process.
An absorbent core ite sheet providing an absorbent construction
according to the above description and may, subsequent to SAP tion and
securement, be bonded to further secure the SAP. As described above, a bonding pattern
applied to the sheet creates pockets of SAP aggregates. For example, a diamond embossing
pattern as described previously in respect to may be employed to bond the outside
nonwoven layers. In alternative embodiments, the ite sheet may be slit and cut
longitudinally to produce multiple core composites or sheets. In such an application, the
source core sheet for slitting may be delivered with uniform thickness and without pockets.
When utilizing hotmelt particles as binder for SAP ving aggregates, the
SAP particle size and quantity relative to hotmelt particles may be a design eration for
improving or preserving SAP performance. Generally, the amount of hotmelt particles must
be adequate for g the SAP. Excess hotmelt particles or material may, however, work to
reduce capacity and absorption rate of the SAP particle. This is due to the hotmelt material
possibly coating or blocking the SAP particle, and as well, restricting movement and
swelling. In preferred embodiments, the ratio of hotmelt particles to SAP particles is one-to-
one.
In further embodiments, the SAP aggregate constitution may include a
combination of SAP particles, in the spherical and/or flake forms, and SAP in the
superabsorbent f1ber form (sometimes referred to as SAF). Specific combinations and ratios
may be ed to achieve desired fluid or absorbent properties, as well as structural
properties. For example, in embodiments wherein a bulky layer is employed with a
combination of spherical SAP and bsorbent fibers, smaller spherical SAP will ate
to and penetrate the open fibrous surface of the bulky nonwoven. In contrast, the
superabsorbent f1bers will tend to settle atop the surface.
[00156] In another embodiment, the SAP aggregate constitution is ted or rather,
infiltrated, by smaller inert particles which position themselves between the larger SAP
particles. This increased spacing increases the bility of the SAP aggregate. The void
volume available within the aggregate is increased due to the spacing. As a result, the SAP
particles located inside the aggregate are less likely to experience gel ng. Preferably,
the spacing particles are inert so as not to alter the SAP properties, and sufficiently small so
as not to significantly increase the volume of the aggregate, the pocket, or core composite.
An example of a suitable inert particle is an ion exchange resin particles (as
also described previously). In this mode, it can be distributed throughout the absorbent
composite, including sections intended as target area. As bed previously, the addition of
ion exchange particles will serve to increase the capacity of the SAP at the target zone and
hout the core because it will reduce the ionic strength of the incoming fluid (urine).
Typical ion exchange resin particle size used in these applications will be about 300-400
microns in size. Another suitable, and readily ble, source of a spacing particle are
microporous silica gel beads. Silica gel is an amorphous form of silicon dioxide that is
synthetically produced in the form of hard regular beads. It has a microporous structure and is
typically used as a high capacity desiccant. The gel beads are available in suitable particle
sizes betweenlSOmicrons - 2000microns or greater. In addition to functioning as a spacer, the
silica gel can also be used as a carrier for other ients such as fragrances and odor
control agents. These ingredients are pre-applied to the microporous beads and will be
contained within the bead when deposited with the SAP.
To rate, provides a general ion of the distribution and
mutual spacing of SAP particles S as found in an absorbent core composite, with and without
the aid of inert les (ii). On the left portion of , a normal distribution of the SAP
particles (S) are shown relatively firmly packed in a given volume or area. Then, a joint
population of inert particles (ii) and SAP (S) is introduced into the same area or volume. As
shown on the right side of , the inert particles (ii) situate themselves n SAP
les (S). As a result, the spacing between SAP particles is increased, even with inert
particles randomly occupying some of the space. There are less SAP particles (S) in the same
area. In , the average dimension (z'.e., diameter) of the inert particles is less than
about 40% of that of the SAP particle (for illustration). It should be noted however, that , shows only the area. The actual space n SAP particles is in three dimension and
thus, the increase in volume (not area) between SAP les (with the inert particles (ii) is
greater (one degree of order higher than area ation).
[00159] In a filrther embodiment, the SAP aggregate constitution may include a water-
soluble particle to perform the spacing filnction. The spacing particle in this constitution will,
however, dissolve upon liquid intake. This serves to provide yet additional void volume, and
to accommodate SAP swell. An example of a suitable source of soluble particle is a
WO 02934
polyvinyl alcohol. A low molecular weight, cold water soluble PVOH may be used (i.e.,
Selv01203 (Sekisui SC), Poval PVA-203 (Kuraray)).
In a yet another ment, n a hotmelt ve is employed, heat
sensitive, volatile particles are employed as spacers or spacing particles. When a bonding
step applies heat to activate the hotmelt, the spacer particle evaporates leaving the SAP, the
hotmelt particles, and onal void space between SAP les (see ). Selection
of suitable volatile particle must, of course, take into consideration le safety and practical
concerns, including the level of energy required to activate the material. The material is
incorporated material in solid form to the SAP mixture for deposition and then vaporizes upon the
ation of heat or . Possible sources are dry ice and iodine.
provides a graphical chart 1300 that illustrates the various
mechanisms described above, and the interactions between SAP aggregate constituents. Each
of four rows or panels of the chart 1300 illustrate the packing (i.e. spacing and distribution) of
SAP particles and non-absorbent particles, including spacing particles, in a entative
portion of the ent composite. The top row (a) relates to the addition of hotmelt particle
to the SAP population. Before bonding, the hotmelt particles occupies a small space between
SAP particles. During bonding, the hotmelt particle melts, leaving space between SAP
particles. As illustrated by the right most frame, SAP later swells to fill up much of the space
between SAP particles. The next row (b) illustrates particle packing when inert les is
added -- to the mix of hotmelt particle and SAP. As shown in the first frame, the inert
particles help to space the ly space SAP, even after the hotmelt transforms to a coating
after bonding. Later, when a SAP particle begin to swell, it can expand into the void left by
the hotmelt particle.
[00162] The next row (c) rates the addition of volatile particles to the mix of
hotmelt and SAP. The volatile particles help to mutually space the SAP particles and
increase permeability. As shown in the rightmost frame, the inert particles continues to help
space the SAP from each other, even during product use and SAP swell. depicts, in
the last row (d), the addition of water soluble particles into the SAP-hotmelt mix. The water
e particles remain in the mixture even when the hotmelt particle disappears after
bonding. The water soluble particles dissolve, however, in use, as the pocket begins to takes
on water content. As shown to the right of , SAP occupies volume between SAP
les and helps to space the particles, but gives up this space to expanding SAP particles
during use.
Each of the tics of FIGS. 16 and 17 illustrates an exemplary system
(1600, 1700) and method for making an absorbent core composite ing to one or more
of the embodiments described above. In a method according to , a sheet or fabric
1625 is dispensed from spool 1620 and carried along a production line on a conveyer belt
1605. The sheet or fabric es the substrate 1620 of the finished absorbent core
composite. In various preferred embodiments, the substrate 1625 is nonwoven thermo c
material. The sheet 1625 is subjected to a riffling or corrugating process by which one surface
of the sheet is etched or scratched to produce riffles or corrugations thereon, as previously
discussed in respect to In this example, a pair of grooved rolls 1686 (one female and
one male) is employed to create the desired corrugation dimensions and pitch. The
corrugations are directed in the machine direction. Adhesive is then applied on the
ated surface in ation for and as required of SAP to be ted on the surface
(see adhesive applicator 1688) In this ment, two SAP dispensers 1680b are
employed serially deposit SAP on the riffled or corrugated e. The first dispenser 1680a
operates to deposit SAP almost all the way across the moving substrate. The second SAP
ser 1680b operates to t SAP onto a central region of the substrate, thereby
supplementing the SAP amounts previously deposited in that region. For some absorbent
composite designs wherein SAP amounts vary in the longitudinal direction, the second SAP
dispenser 1680b may be operated intermittently. See, for example, the core designs of
and the accompanying description. The second SAP deposited may also be of a type different
from the first SAP deposited, and\or contain a constitution different from the first deposit
(e.g., contain non-SAP materials not provided with the first SAP). The second SAP may, for
example, exhibit properties ularly advantageous for use in the central region of the
finished core. In this embodiment, the SAP is secured on the sheet 1625 and the sheet 1625 is
secured to the conveyor belt 1605 by a vacuum system applying suction to the sheet 1625.
Referring again to , a second sheet or fabric 1625 is simultaneously
dispensed from a second supply spool and carried along a production line on a second
conveyer belt 1607. In various embodiments, the second fabric 1655 is a nonwoven material
that provides the top substrate or cover layer for the absorbent core composite. In this
embodiment, the top substrate is also elongatable. Accordingly, the second sheet 1655 is also
subjected to a riffling or corrugating process. Thereafter, adhesive may be applied to the
riffled or corrugated surface, before the sheet meets the main production line 1605 and
engages the now ned first sheet 1625. At this juncture, a three-layered composite is
formed and advanced on the production line. In the embodiment shown, the composite is
passed between a pair of embossing rollers 1660 to apply a desired bonding pattern on the
ite and form pockets of SAP ates. The resultant ent composite may,
therefore, feature a plurality of spaced-apart pockets having a top and bottom elongatable
substrates. The pockets in the central region may filler and contain more SAP than pockets
located to the side of the central region.
illustrates a further variation of the system and method rated by
(wherein like reference numerals are used to indicate like elements). Like the
ent composite described in respect to , the absorbent composite made by this
system 1700 and process provides a plurality of s of SAP aggregate having an
elongatable top layer and an elongatable bottom layer. The absorbent composite employs,
however, a third or intermediate layer that is not elongatable. The intermediate layer may be
provided by tissue material, which is considered breakable when wetted. Such an absorbent
ite constructions is rated by . As shown in , a third ate
1765 is applied intermediate the two sheet 1725, 1735 and more specifically over the SAP-
lined first sheet. SAP is then deposited on the non-corrugated surface of the intermediate
sheet 1765 before the third sheet 1755 is d over the then SAP-lined intermediate sheet
1765. After engaging embossing rollers 1760 for bonding, the resultant ent composite
features a plurality of spaced apart pockets of SAP aggregate, n the three-layered
pocket is made expandable top and bottom nonwoven ates.
[00166] It is noted that in the various exemplary descriptions provide above, there are
occasional mention of a corresponding steps or processes in making the core composite (or
disposable absorbent article). Although the description may not necessarily be provided from
the perspective of cturing product, it is believed that various cturing or core
preparation methodologies, and equipment associated therewith, will become apparent from a
reading of the various descriptions, perhaps in conjunction with common knowledge in the
art or the references cited herewith.
The foregoing description has been presented for purposes of illustration and
description of preferred embodiments. This description is not intended to limit associated
concepts to the various systems, apparatus, structures, and methods specifically described
herein. For example, the various pocket designs may be employed in various types of
disposable ent articles. Moreover, the various mechanisms of increasing void space or
volume may be used in different combination, and at varying degrees, as required for the
absorbency demands of a product.. The embodiments described and illustrated herein are
r intended to explain the best and preferred modes for practicing the system and
methods, and to enable others skilled in the art to utilize same and other embodiments and
with various modifications required by the ular applications or uses of the present
invention.
Claims (15)
1. An absorbent core composite for incorporation into a disposable absorbent article, the absorbent core composite comprising: a first material layer having an outside surface forming a bodyside outer surface of the absorbent core composite; a second material layer having an outside surface forming an opposite outer surface of said absorbent core composite, n the first material layer is a nonwoven having a density of from 0.01 to 0.03 g/cc and the second material layer is a nonwoven having a density that is higher than the density of the first material layer; and a first layer of absorbent particles disposed between said outer surfaces of the absorbent composite and having a first average size dimension; a second layer of absorbent particles disposed between said outer surfaces of the absorbent composite, said absorbent particles of said second layer having a second e size dimension that is less than the first average size dimension of the first layer of ent particles; and wherein said first layer of absorbent particles are situated substantially in the first material layer and the second layer of absorbent particles are situated substantially in the second material layer.
2. A method of forming an absorbent ite for incorporation into a disposable absorbent article, said method sing: providing a first material layer, wherein the first material layer is a nonwoven ha ving a y of from 0.01 to 0.03 g/cc; positioning a second material layer h the first material layer, wherein the second material layer is a nonwoven having a density that is higher than the density of the first material layer; providing a supply of absorbent particles composed of a first population of absorbent particles having a first average size dimension and a second population of absorbent particles having a second average size dimension that is less than the first average size ion; and depositing the first and second populations of absorbent particles onto the first al layer such that absorbent particles of the first population are ined in the first material layer and the ent les of the second population filter through the first material layer and settle in the second material layer.
3. The method of claim 2, wherein the second material layer has a density of from 0.03 to .08 g/cc.
4. The method of claim 2, r comprising conveying the first and second al layers to an area of travel wherein said depositing of said absorbent particles onto the first material layer occurs.
5. The method of claim 4, wherein said first and second material layers are moved past said area of travel such that said second population of absorbent particles filters through the first material layer as said first and second material layers are conveyed after said depositing.
6. The method of claim 2, further comprising energizing the first and second material layers after depositing to promote said filtering.
7. The method of claim 6, wherein said energizing es vibrating said first and second material layers.
8. The method of claim 2, further comprising: positioning an intermediate material layer of nonwoven intermediate said first and second al layers, wherein said first, intermediate, and second material layers have a density of 0.01 to 0.03 g/cc, 0.03 to .08 g/cc, and 0.09 to 0.12 g/cc, respectively.
9. The method of claim 8, further comprising ing an intermediate population of absorbent particles, wherein the average size dimension of said first, intermediate, and second populations, in microns, are 0-300, 0, and 600-850, tively; and n said depositing includes simultaneously depositing said first, second, and intermediate populations of absorbent particles such that said second population of absorbent particle filters through the first and intermediate material layers to the second material layer and said intermediate population of absorbent particles filter through the first al layer and settle in the ediate material layer.
10. An absorbent core composite for incorporation into a disposable absorbent e, the absorbent core composite comprising: a first material layer having an outside surface forming a bodyside outer surface of the absorbent core composite; a second material layer having an outside surface forming an opposite outer surface of said absorbent core ite, wherein the first and second material layers are nonwovens, wherein the second material layer has a density that is higher than the density of the first material layer, and wherein the y of the second material layer is from 0.03 to 0.08 g/cc; a first layer of absorbent particles ed between said outer es of the absorbent composite and having a first e size dimension; a second layer of absorbent particles disposed between said outer surfaces of the absorbent composite, said absorbent particles of said second layer having a second average size dimension that is less than the first average size dimension of the first layer of absorbent particles; and wherein said first layer of absorbent les are situated substantially in the first material layer and the second layer of absorbent particles are situated substantially in the second material layer.
11. A method of forming an absorbent composite for incorporation into a disposable absorbent article, said method comprising: providing a first material layer, wherein the first material layer is a nonwoven ; positioning a second material layer beneath the first material layer, wherein the second material layer is a nonwoven having a density that is higher than the density of the first material layer , and wherein the density of the second material layer is from 0.03 to 0.08 g/cc; providing a supply of ent particles composed of a first population of absorbent particles having a first e size dimension and a second population of ent particles having a second average size dimension that is less than the first average size dimension; and depositing the first and second populations of absorbent les onto the first material layer such that absorbent particles of the first population are maintained in the first material layer and the absorbent particles of the second population filter through the first material layer and settle in the second material layer.
12. The method of claim 11, further comprising conveying the first and second material layers to an area of travel wherein said depositing of said absorbent particles onto the first al layer occurs.
13. The method of claim 12, wherein said first and second al layers are moved past said area of travel such that said second population of absorbent particles filters through the first material layer as said first and second material layers are conveyed after said depositing.
14. The method of claim 11, further comprising energizing the first and second al layers after depositing to promote said filtering.
15. The method of claim 14, n said energizing includes vibrating said first and second material layers. WO 02934
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361842961P | 2013-07-03 | 2013-07-03 | |
| US61/842,961 | 2013-07-03 | ||
| US201361843986P | 2013-07-09 | 2013-07-09 | |
| US61/843,986 | 2013-07-09 | ||
| PCT/US2014/045027 WO2015002934A2 (en) | 2013-07-03 | 2014-07-01 | An absorbent composite, an absorbent article employing the same, and methods, systems, and apparatus for making the absorbent composite and/or article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ716077A NZ716077A (en) | 2020-11-27 |
| NZ716077B2 true NZ716077B2 (en) | 2021-03-02 |
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