JP6118158B2 - Absorber and absorbent article provided with the same - Google Patents

Description

  The present invention relates to an absorbent body and an absorbent article including the same.

  As an absorbent article, a liquid-permeable top sheet, a liquid-impermeable back sheet, a storage layer that temporarily stores liquid, an absorbent core that absorbs liquid stored in the storage layer, and an absorbent Absorbent articles including a coating layer that covers a core are known (Patent Documents 1 to 4). According to the absorbent articles described in Patent Literatures 1 to 4, the storage layer temporarily stores the liquid, and the stored liquid is distributed and supplied to the absorbent core, whereby an efficient liquid in the absorbent core is obtained. Absorption can be realized.

  On the other hand, as a heat-adhesive conjugate fiber for airlaid nonwoven fabric, a modified polyolefin graft-polymerized with a vinyl monomer containing an unsaturated carboxylic acid or unsaturated carboxylic acid anhydride is used as a sheath component, and a resin having a higher melting point than the modified polyolefin is used as a core. A core-sheath type composite fiber as a component is known (Patent Documents 5 and 6).

International Publication WO2004 / 071363 Pamphlet International Publication WO2004 / 071539 Pamphlet International Publication WO2007 / 057869 Pamphlet International Publication WO2008 / 155711 Pamphlet Japanese Patent No. 4221849 JP 2004-270041 A

  In the absorbent articles described in Patent Literatures 1 to 4, since the storage layer and the coating layer are usually bonded using an adhesive such as a hot melt adhesive, the storage layer is stored in a use environment (particularly in a wet state). There is a possibility that the layer and the covering layer may be separated.

  On the other hand, the core-sheath type composite fibers described in Patent Documents 5 and 6 are known to have good adhesion to cellulosic fibers, but their availability as a constituent component of the reservoir layer is known. There wasn't.

  Therefore, the present invention is an absorbent body having a storage layer that temporarily stores liquid, an absorbent core that absorbs the liquid stored in the storage layer, and a coating layer that covers the absorbent core. It is an object of the present invention to provide an absorbent body capable of preventing peeling between a storage layer and a coating layer that may occur in an environment (particularly in a wet state), and an absorbent article including the same.

In order to solve the above-described problems, the present invention provides a storage layer that temporarily stores liquid, an absorbent core that absorbs the liquid stored in the storage layer, and a surface on the storage layer side of the absorbent core. An absorbent body having a coating layer to be coated, and an integral part for integrating the storage layer and the coating layer, wherein the storage layer comprises a cellulose-based water absorbent fiber, an unsaturated carboxylic acid, and an unsaturated carboxylic acid. Thermoplastic resin fibers containing an anhydride or a mixture thereof as a monomer component, the absorbent core contains a superabsorbent polymer material, and the coating layer contains cellulosic water absorbent fibers, Provide an absorber.
Further, the present invention is an absorbent article comprising a liquid permeable layer, a liquid impermeable layer, and the absorbent body of the present invention, wherein the storage layer comprises the liquid permeable layer and the absorbent core. The absorbent article is provided, wherein the absorbent body is provided between the liquid-permeable layer and the liquid-impermeable layer so as to be positioned therebetween.

  According to the present invention, there is provided an absorbent body having a reservoir layer that temporarily stores liquid, an absorbent core that absorbs the liquid stored in the reservoir layer, and a coating layer that covers the absorbent core. Provided are an absorbent body capable of preventing separation between a storage layer and a coating layer that may occur in an environment (particularly in a wet state), and an absorbent article including the same.

FIG. 1 is a perspective view of a disposable diaper according to an embodiment of the absorbent article of the present invention. FIG. 2 is a developed plan view showing a state in which the connection between the front surface portion and the rear surface portion is released in the disposable diaper of FIG. 1. FIG. 3 is an exploded perspective view of the disposable diaper of FIG. Fig.4 (a) is a top view of the absorber which the disposable diaper of FIG. 1 comprises, FIG.4 (b) is the sectional view on the AA line of Fig.4 (a). FIG. 5 is a diagram showing an embodiment of the manufacturing process of the absorbent body of the present invention. FIGS. 6A and 6B are diagrams showing an SJ belt press used in the examples.

Hereinafter, the absorbent body and absorbent article of the present invention will be described.
The absorber according to aspect 1A includes a storage layer that temporarily stores liquid, an absorbent core that absorbs the liquid stored in the storage layer, and a coating layer that covers a surface of the absorbent core on the storage layer side. And an absorbent body that integrates the reservoir layer and the coating layer, wherein the reservoir layer is a cellulosic water absorbent fiber (hereinafter sometimes abbreviated as "water absorbent fiber"); A thermoplastic resin fiber (hereinafter sometimes abbreviated as “thermoplastic resin fiber”) containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride or a mixture thereof as a monomer component, and the absorbent core The absorbent body contains a highly water-absorbing polymer material, and the coating layer contains cellulosic water-absorbing fibers (hereinafter sometimes abbreviated as “water-absorbing fibers”).

  In the absorbent body according to aspect 1A, since the storage layer and the coating layer are integrated by the integrated portion, peeling between the storage layer and the coating layer that may occur in the use environment (particularly in a wet state) is prevented. Can do. In addition, since the strength of the reservoir (especially when wet) is improved by an advanced network formed between the fibers of the reservoir, the reservoir and the coating layer that may be caused by a decrease in the strength of the reservoir Can be prevented.

  In the absorbent body according to aspect 1A, the integrated part is formed by heat-treating the storage layer together with the coating layer. Examples of the heat treatment include a heat embossing process and a heating fluid injection process, and examples of the heating fluid injection process include a high-pressure steam injection process and a heated air injection process. When the storage layer is heat-treated together with the coating layer, the thermoplastic resin fibers contained in the storage layer are thermally fused with the water-absorbing fibers contained in the coating layer, and the storage layer and the coating layer are integrated. This increases the interfacial peel strength between the reservoir layer and the coating layer. In particular, a thermoplastic resin fiber containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride or a mixture thereof as a monomer component has a high bonding strength with a cellulosic water-absorbing fiber by thermal fusion, so that the coating layer is thermoplastic. Even if the resin is not contained or the amount of the thermoplastic resin contained in the coating layer is reduced, a sufficient interfacial peel strength can be obtained. Therefore, it is possible to prevent a decrease in liquid transferability from the reservoir layer to the absorbent core due to the hydrophobicity of the thermoplastic resin contained in the coating layer.

  In the absorbent body according to the aspect 1A, the coating layer is a second coating that covers the surface of the absorbent core on the side opposite to the storage layer side in addition to the first coating portion that covers the surface of the absorbent core on the storage layer side. You may have the coating | coated part. In this case, as long as the integrated part integrates the reservoir layer and the first covering part, the integrated part may integrate the second covering part together with the reservoir layer and the first covering part. It does not have to be integrated. Moreover, the absorber which concerns on aspect 1A is the 2nd coating | cover which coat | covers the surface on the opposite side to the storage layer side of an absorptive core in addition to the 1st coating layer which coat | covers the surface by the side of the storage layer of an absorptive core. It may have a layer. In this case, as long as the storage unit and the first coating layer are integrated, the integration unit may integrate the second coating layer together with the storage layer and the first coating layer, or the second coating layer. It does not have to be integrated.

  In the absorbent body according to aspect 1A, it is preferable that the fibers contained in the reservoir layer are bonded to each other (aspect 2A). In the absorbent body according to the aspect 2A, since the advanced network is formed between the fibers due to adhesion between the constituent fibers of the storage layer, the strength of the storage layer (particularly the strength when wet) is improved. Therefore, the absorber which concerns on aspect 2A can prevent peeling with the reservoir layer and the coating layer which may arise by the strength fall of a reservoir layer. Examples of the bonding mode include bonding between thermoplastic resin fibers or between thermoplastic resin fibers and water-absorbing fibers by thermal fusion of thermoplastic resin fibers, between thermoplastic resin fibers by hydrogen bonding, between water-absorbing fibers or heat. Examples include adhesion between a plastic resin fiber and a water absorbent fiber. When the reservoir layer includes other fibers, the thermoplastic resin fibers and / or the water-absorbing fibers may be bonded to the other fibers. The hydrogen bond is cut by the liquid absorbed in the reservoir.

  In the absorbent body according to aspect 1A or 2A, the interfacial peel strength during drying of the reservoir layer and the coating layer is 1.75 to 4.23 N / 25 mm, and the interfacial peel strength during wetness of the reservoir layer and the coating layer is It is preferably 1.05 to 2.63 N / 25 mm (Aspect 3A). The absorbent body according to aspect 3A can prevent peeling between the reservoir layer and the coating layer through before and after liquid absorption (that is, not only when dry but also when wet).

  In the absorbent body according to aspects 1A to 3A, the mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer is preferably 1/9 to 5/5 (Aspect 4A). In the absorbent body according to aspect 4A, the lower limit of 1/9 is defined from the viewpoint of the degree of network formation between fibers, and the mass ratio of thermoplastic resin fibers to water-absorbing fibers is 1/9 or more. Since a sophisticated network is formed between the fibers, sufficient strength (especially when wet) can be imparted to the reservoir, which can result from a reduction in the strength of the reservoir. Peeling from the layer can be prevented. On the other hand, the upper limit of 5/5 is defined from the viewpoint of the liquid absorbability of the reservoir, and if the mass ratio of the thermoplastic resin fiber to the water absorbent fiber is 5/5 or less, the reservoir is sufficient. Liquid absorptivity (liquid permeability and diffusibility) can be imparted, which allows the liquid temporarily stored in the reservoir to be efficiently distributed and supplied to the absorbent core. Can be absorbed.

The absorber which concerns on aspect 4A WHEREIN: It is preferable that the density of the said storage layer is 0.06-0.14 g / cm < ³ > (aspect 5A). When the mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer is 1/9 to 5/5, the reservoir layer having a density of 0.06 to 0.14 g / cm ³ is sufficient for the reservoir layer. Liquid absorbency can be imparted.

  In the absorbent body according to aspect 5A, the storage layer is obtained by injecting high-pressure steam into a mixed material containing the cellulosic water-absorbing fiber and the thermoplastic resin fiber to increase the density. It is preferable that there is (Aspect 6A). In the absorbent body according to aspect 6A, the density of the reservoir is adjusted to a desired range by densification using high-pressure steam injection. When high-pressure water vapor is injected into the mixed material, the water vapor penetrates into the mixed material and forms hydrogen bonds (for example, between water-absorbing fibers, between thermoplastic resin fibers, between water-absorbing fibers and thermoplastic resin fibers, etc.). (Hydrogen bonds) are broken, and the mixed material is softened. Therefore, the pressure required for densification decreases, and the density of the softened mixed material can be easily adjusted. When the density-adjusted mixed material is dried and hydrogen bonds are re-formed, the elastic recovery (increase in volume) of the fibers is suppressed, and the density of the reservoir is maintained within a certain range. Aspect 6A is particularly suitable when an unsaturated carboxylic acid anhydride (for example, maleic anhydride or a derivative thereof) is contained as a monomer component in the thermoplastic resin fiber. When the unsaturated carboxylic acid anhydride group contained in the thermoplastic resin fiber reacts with water vapor to form an unsaturated carboxylic acid group, the number of oxygen atoms capable of forming hydrogen bonds increases. Elastic recovery (increase in bulk) is effectively suppressed.

In the absorber according to the aspect 5A or 6A, it is preferable that the basis weight of the reservoir layer is 40 to 900 g / m ² (Aspect 7A). If the basis weight is less than 40 g / m ^2, the fibers of the thermoplastic resin fibers is insufficient, while the strength of the reservoir (especially strength when wet) may be lowered, if it exceeds 900 g / m ² The fiber amount of the thermoplastic resin fiber becomes excessive, and the rigidity of the reservoir layer may be too high.

  In the absorbent body according to Embodiments 1A to 7A, the thermoplastic resin fiber is a modified polyolefin graft-polymerized with a vinyl monomer containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride, or a mixture thereof, or the modified polyolefin and other A core-sheath composite fiber having a sheath polymer as a mixed polymer with a resin and a resin having a melting point higher than that of the modified polyolefin as a core component is preferable (Aspect 8A).

  In the absorber according to Embodiments 1A to 8A, it is preferable that the unsaturated carboxylic acid, unsaturated carboxylic acid anhydride, or a mixture thereof is maleic acid or a derivative thereof, maleic anhydride or a derivative thereof, or a mixture thereof. (Aspect 9A).

  In the absorbent body according to aspects 1A to 9A, the difference between the maximum tensile strength when dried and the maximum tensile strength when wet in the reservoir is preferably 1 to 5 N / 25 mm (Aspect 10A). In the absorbent body according to the aspect 10A, the storage layer has sufficient strength to maintain an integrated structure with the coating layer through before and after liquid absorption (that is, not only when dry but also when wet).

  The absorbent article which concerns on aspect 1B is an absorbent article provided with the liquid-permeable layer, the liquid-impermeable layer, and the absorber which concerns on any one aspect of aspect 1A-10A, Comprising: The said storage layer is In the absorbent article, the absorber is provided between the liquid permeable layer and the liquid impermeable layer so as to be positioned between the liquid permeable layer and the absorbent core. The absorbent article which concerns on aspect 1B can exhibit the effect similar to the absorber which concerns on aspect 1A-10A according to the aspect of the absorber which comprises.

The kind and application of the absorbent article of the present invention are not particularly limited. Examples of absorbent articles include disposable diapers, sanitary napkins, panty liners, incontinence pads, and hygiene articles such as sweat removal sheets. These may be intended for humans and other than humans such as pets. Animals may be targeted. The liquid to be absorbed by the absorbent article of the present invention is not particularly limited, and examples thereof include liquid excrement and body fluid of the wearer.
Hereinafter, an embodiment of the absorbent article of the present invention will be described based on the drawings, taking a disposable diaper as an example.

  As shown in FIG.1 and FIG.2, the diaper 1 which concerns on one Embodiment of the absorbent article of this invention is the front part 11 applied to a wearer's abdomen, and the intermediate part 12 applied to a wearer's crotch part, And a rear surface portion 13 applied to the wearer's buttocks and / or back. 2, the X-axis direction is the width direction of the diaper 1 in the unfolded state, the Y-axis direction is the longitudinal direction of the diaper 1 in the unfolded state, and the plane direction extending in the X-axis Y-axis direction is the diaper 1 in the unfolded state. Corresponds to the plane direction. The same applies to the other drawings.

  As shown in FIG. 1, in the joint portions 14 a and 14 b, the side portions 111 a and 111 b of the front surface portion 11 and the both side portions 131 a and 131 b of the rear surface portion 13 are joined to each other. A waist opening is formed by the end portion 132 of the surface portion 13, and leg openings are formed by both side portions 121 a and 121 b of the intermediate portion 12, and the diaper 1 has a pants-type shape. .

  As shown in FIGS. 1 to 3, the diaper 1 includes a liquid-permeable top sheet 2, a liquid-impermeable back sheet 3, and an absorbent body 4 provided between the top sheet 2 and the back sheet 3. It has. Hereinafter, these members will be described.

<Top sheet>
The top sheet 2 is an example of a liquid permeable layer.
As shown in FIGS. 1-3, a part of top sheet 2 (a part of arrangement | positioning area | region of the absorber 4) is exposed from the opening part 61 formed in the approximate center of the cover sheet 6 mentioned later, and the diaper 1 It constitutes the skin side surface. The region where the absorber 4 is disposed is a region where the absorber 4 overlaps the top sheet 2 when the absorber 4 is projected onto the top sheet 2, and in the present embodiment is substantially the entire top sheet 2 (FIG. 2).

  The top sheet 2 is a liquid-permeable sheet that allows the liquid excrement of the wearer to pass therethrough. Examples of the top sheet 2 include a nonwoven fabric, a woven fabric, a synthetic resin film in which liquid permeation holes are formed, a net-like sheet having a mesh, and the like, preferably a nonwoven fabric.

  Examples of the nonwoven fabric include an air-through nonwoven fabric, a spunbond nonwoven fabric, a point bond nonwoven fabric, a spunlace nonwoven fabric, a needle punched nonwoven fabric, a melt blown nonwoven fabric, and a combination thereof (for example, SMS).

  Examples of the fibers constituting the nonwoven fabric include natural fibers (wool, cotton, etc.), recycled fibers (rayon, acetate, etc.), inorganic fibers (glass fibers, carbon fibers, etc.), synthetic resin fibers (polyethylene, polypropylene, polybutylene, ethylene). -Polyolefin such as vinyl acetate copolymer, ethylene-ethyl acrylate copolymer, ethylene-acrylic acid copolymer, ionomer resin; polyester such as polyethylene terephthalate, polybutylene terephthalate, polytrimethylene terephthalate, polylactic acid; And polyamides such as nylon). Examples of the form of the fibers constituting the nonwoven fabric include core / sheath fibers, side-by-side fibers, island / sea fibers, etc .; hollow fibers; flat, Y-shaped, C-shaped, etc. Atypical fiber; three-dimensional crimp fiber of latent crimp or actual crimp; split fiber divided by physical load such as water flow, heat, embossing and the like.

  Examples of the nonwoven fabric manufacturing method include a method of forming a web (fleece) and physically and chemically bonding fibers. Examples of the web forming method include a spunbond method and a dry method (card). Method, spunbond method, melt blown method, airlaid method, etc.), wet method, etc., and examples of the bonding method include thermal bond method, chemical bond method, needle punch method, stitch bond method, spunlace method, etc. It is done. In addition to the nonwoven fabric produced in this manner, a spunlace formed into a sheet shape by a hydroentanglement method may be used as the top sheet 2. Moreover, the nonwoven fabric which provided the unevenness | corrugation on the skin side surface (For example, the nonwoven fabric which formed the unevenness | corrugation in the upper layer side by shrink | contracting the lower layer side containing a heat shrink fiber etc., and the unevenness | corrugation was formed by applying air at the time of web formation Nonwoven fabric or the like) may be used as the top sheet 2. Thus, by forming unevenness on the skin side surface, the contact area between the top sheet 2 and the skin is reduced.

  The thickness, basis weight, density, and the like of the top sheet 2 are appropriately adjusted as long as the liquid excrement of the wearer can permeate. When using a non-woven fabric as the top sheet 2, the fineness, fiber length, density, basis weight, thickness, etc. of the non-woven fabric are appropriately adjusted from the viewpoints of permeability of liquid excrement, touch, and the like.

  From the viewpoint of improving the concealability of the top sheet 2, the nonwoven fabric used as the top sheet 2 may contain an inorganic filler such as titanium oxide, barium sulfate, or calcium carbonate. When the nonwoven fabric fiber is a core-sheath type composite fiber, an inorganic filler may be contained only in the core, or only in the sheath.

<Back sheet>
The backsheet 3 is an example of a liquid impermeable layer.
As shown in FIGS. 1 to 3, the back sheet 3 constitutes the clothing side surface of the diaper 1.
The back sheet 3 is a liquid-impermeable sheet that can prevent leakage of liquid excretion absorbed and retained by the absorber 4. Examples of the back sheet 3 include waterproof nonwoven fabric (for example, point bond nonwoven fabric, spun bond nonwoven fabric, spun lace nonwoven fabric, etc.), synthetic resin (for example, polyethylene, polypropylene, polyethylene terephthalate, etc.) film, nonwoven fabric and synthetic resin. Examples include a composite sheet with a film.

  The material, thickness, basis weight, density, and the like of the backsheet 3 can be adjusted as appropriate within a range in which leakage of liquid excretion absorbed and retained by the absorber 4 can be prevented. The back sheet 3 preferably has air permeability or moisture permeability in addition to liquid impermeability in order to reduce stuffiness when worn.

<Absorber>
As shown in FIG. 2, the absorber 4 is disposed so as to reach the rear surface portion 13 from the front surface portion 11 through the intermediate portion 12.

  As shown in FIGS. 3 and 4, the absorbent body 4 has a storage layer 41 that temporarily stores liquid excrement that has passed through the top sheet 2, and an absorptivity that absorbs liquid excrement stored in the storage layer 41. A core 42; core wraps 43a and 43b that cover the surface of the absorbent core 42 on the side of the storage layer 41 and the surface on the opposite side; and an integrated portion 44 that integrates the storage layer 41 and the core wrap 43a. The liquid excrement passing through the top sheet 2 is temporarily stored in the storage layer 41, then distributed and supplied from the storage layer 41 to the absorbent core 42, and absorbed and held by the absorbent core 42. . As shown in FIG. 3, the absorbent body 4 is provided between the top sheet 2 and the back sheet 3 so that the storage layer 41 is located between the top sheet 2 and the absorbent core 42. In FIG. 3, the core wraps 43a and 43b are not shown.

  As shown in FIG. 4, the storage layer 41 is directly laminated on the core wrap 43a and has an interface with the core wrap 43a. This separation of the interface is prevented by the integrated portion 44 as will be described later.

  The storage layer 41 is a thermoplastic resin fiber containing a cellulose-based water-absorbing fiber (hereinafter sometimes abbreviated as “water-absorbing fiber”) and an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride, or a mixture thereof as monomer components. (Hereinafter sometimes abbreviated as “thermoplastic resin fiber”). The water-absorbing fibers are mainly involved in the liquid absorbency and storage properties of the reservoir layer 41, and the thermoplastic resin fibers are mainly involved in the strength of the reservoir layer 41 (particularly the strength when wet).

  The water absorbing fibers and the thermoplastic resin fibers are contained in the storage layer 41 in a mixed state. Intersections between fibers (for example, intersections between thermoplastic resin fibers, intersections between thermoplastic resin fibers and water-absorbing fibers) are bonded by thermal fusion of the thermoplastic resin fibers. Further, the fibers are mechanically entangled and bonded by hydrogen bonds formed between the thermoplastic resin fibers, between the water absorbent fibers, or between the thermoplastic resin fibers and the water absorbent fibers. When the storage layer 41 includes other fibers, the thermoplastic resin fibers and / or the water-absorbing fibers may be bonded to the other fibers.

  The heat fusion is performed, for example, by heating a mixed material containing water-absorbing fibers and thermoplastic resin fibers at a temperature equal to or higher than the melting point of the thermoplastic resin fibers. The heating temperature can be appropriately adjusted according to the type of thermoplastic resin fiber. The temperature above the melting point of the thermoplastic resin fiber may be at or above the temperature at which a part of the thermoplastic resin fiber melts. For example, when the thermoplastic resin fiber is a core-sheath type composite fiber, the temperature at which the sheath component melts That is all you need.

  Since an advanced network is formed between the fibers by bonding of the fibers contained in the storage layer 41, the strength of the storage layer 41 (particularly the strength when wet) is improved. Thereby, in use environment (especially wet state), peeling with the storage layer 41 and the coating layer 43a which may be produced by the strength fall of the storage layer 41 can be prevented.

  The mass ratio (thermoplastic resin fiber / water absorbent fiber) of the thermoplastic resin fiber to the water absorbent fiber in the storage layer 41 is preferably 1/9 or more. The lower limit of 1/9 is defined in terms of the degree of network formation between fibers, and when the mass ratio of the thermoplastic resin fiber to the water-absorbing fiber is 1/9 or more, an advanced network is formed between the fibers. Since it is formed, sufficient strength (particularly wet strength) can be imparted to the storage layer 41, thereby causing separation of the storage layer 41 and the coating layer 43 a that may be caused by a decrease in strength of the storage layer 41. Can be prevented. On the other hand, the upper limit of 5/5 is defined from the viewpoint of the liquid absorbability of the storage layer 41. If the mass ratio of the thermoplastic resin fiber to the water absorbent fiber is 5/5 or less, Sufficient liquid absorptivity (liquid permeability and diffusibility) can be imparted, whereby liquid excrement temporarily stored in the reservoir 41 is efficiently distributed and supplied to the absorbent core for absorption Can be efficiently absorbed by the sex core.

  As the mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer 41 (thermoplastic resin fibers / water-absorbent fibers) increases, the degree of inter-fiber network formation and strength (particularly strength when wet) of the reservoir layer 41 increases. . For example, the mass ratio of the thermoplastic resin fiber to the water absorbent fiber is 1/9, 1.5 / 8.5, 2/8, 2.5 / 7.5, 3/7, 3.5 / 6.5. As the size increases to 4/6 and 4.5 / 5.5, the inter-fiber network formation degree and strength of the storage layer 41 increase. Therefore, 1/9, 1.5 / 8.5, 2/8, 2.5 / 7.5, 3/7, 3.5 / 6.5, 4/6, 4.5 / 5.5 The mass ratio may have significance as the lower limit of the mass ratio of the thermoplastic resin fibers to the water-absorbing fibers from the viewpoint of increasing the degree of fiber network formation and strength of the reservoir layer 41.

  The upper limit of the mass ratio (thermoplastic resin fiber / water absorbent fiber) of the thermoplastic resin fiber to the water absorbent fiber in the reservoir layer 41 is preferably 5/5. The upper limit of 5/5 is defined from the viewpoint of the liquid absorbability of the storage layer 41. When the mass ratio of the thermoplastic resin fiber to the water absorbent fiber is 5/5 or less, the storage layer 41 is sufficient. Liquid absorbency (liquid permeability and diffusibility) can be imparted. Therefore, the storage layer 41 can efficiently distribute and supply the liquid excrement stored temporarily to the absorbent core 42, thereby efficiently absorbing the liquid excrement in the absorbent core 42. It becomes feasible.

  As the mass ratio of the thermoplastic resin fibers to the water absorbent fibers in the reservoir layer 41 (thermoplastic resin fibers / water absorbent fibers) decreases, the influence of the hydrophobicity of the thermoplastic resin fibers decreases, and the liquid absorbency of the reservoir layer 41 increases. Become. For example, the mass ratio of the thermoplastic resin fiber to the water absorbent fiber is 5/5, 4.5 / 5.5, 4/6, 3.5 / 6.5, 3/7, 2.5 / 7.5. As 2/8 and 1.5 / 8.5 are reduced, the liquid absorbency of the reservoir 41 is increased. Therefore, 5/5, 4.5 / 5.5, 4/6, 3.5 / 6.5, 3/7, 2.5 / 7.5, 2/8, 1.5 / 8.5 The mass ratio may have significance as the upper limit of the mass ratio of the thermoplastic resin fiber to the water-absorbent fiber from the viewpoint of increasing the liquid absorbency of the storage layer 41.

  The mass ratio of the thermoplastic resin fibers to the water absorbent fibers in the reservoir layer 41 (thermoplastic resin fibers / water absorbent fibers) is determined by the degree of network formation between fibers in the reservoir layer 41, strength (particularly strength when wet), and liquid absorbency. From the viewpoint, it is preferably 1/9 to 5/5, more preferably 2/8 to 4/6.

  The desired strength (particularly wet strength) is adjusted by adjusting the mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer 41, and then the manufacturing conditions of the reservoir layer 41 (for example, the heating conditions during thermal fusion) ) Etc. can be realized. For example, with respect to the fiber material in which the mass mixing ratio of the thermoplastic resin fiber to the water-absorbing fiber is 1/9 or more, hot air at 130 to 220 ° C., preferably 140 to 180 ° C., is supplied with an air volume of 2.5 to 30 m / sec. The desired strength (particularly strength when wet) can be achieved by spraying at a rate of 5 to 20 m / sec, preferably 0.5 to 60 seconds, and preferably 5 to 30 seconds. The blowing of hot air can be performed by, for example, an air-through method. Note that the blowing of hot air is an example of heat treatment. The heat treatment is not particularly limited as long as it can be heated to a temperature equal to or higher than the melting point of the thermoplastic resin fiber. The heat treatment can be performed using a heat medium such as microwaves, steam, infrared rays, etc. in addition to hot air.

The density of the reservoir layer 41 is preferably 0.06~0.14g / cm ^3, more preferably 0.07~0.12g / cm ^3, even more preferably 0.08~0.1g / cm ³ . When the mass ratio of the thermoplastic resin fiber to the water-absorbing fiber in the reservoir layer 41 is 1/9 to 5/5, the reservoir layer 41 has a density of 0.06 to 0.14 g / cm ^3. Sufficient liquid absorbability can be imparted.

The density of the reservoir 41 is calculated based on the following formula.
D (g / cm ³ ) = B (g / m ² ) / T (mm) × 10 ⁻³
[In formula, D, B, and T represent the density, basic weight, and thickness of the storage layer 41, respectively. ]

The basis weight (g / m ² ) of the reservoir 41 is calculated based on the following formula.
Three sample pieces of 100 mm × 100 mm are cut out from the reservoir layer 41, and the mass of each sample piece in a standard state (temperature 23 ± 2 ° C., relative humidity 50 ± 5%) is directly indicated (for example, manufactured by Kensei Kogyo Co., Ltd.) The mass (g / m ² ) per unit area of the reservoir 41 calculated by the electronic balance HF-300) and calculated from the average value of the three measured values is taken as the basis weight of the reservoir 41.
In addition, regarding the measurement of the basic weight of the reservoir 41, the measurement conditions described in ISO 9073-1 or JIS L 1913 6.2 are adopted for the measurement conditions not particularly specified above.

The measurement of the thickness (mm) of the storage layer 41 is performed as follows.
In a standard state (temperature 23 ± 2 ° C., relative humidity 50 ± 5%) by a thickness gauge (for example, FS-60DS, manufactured by Daiei Scientific Instruments Co., Ltd., measurement surface 44 mm (diameter), measurement pressure 3 g / cm ² ). Pressurize five different parts of the reservoir 41 (when using the thickness gauge FS-60DS, the diameter of each part is 44 mm) at a constant pressure of 3 g / cm ² , measure the thickness after 10 seconds of pressure at each part, The average value of the five measured values is taken as the thickness of the reservoir 41.

  The density of the storage layer 41 can be adjusted to a desired range by increasing the density of the mixed material containing water-absorbing fibers and thermoplastic resin fibers. In order to maintain the density of the reservoir 41 within a certain range, it is necessary to suppress the elastic recovery of the fibers and maintain the bulk of the reservoir 41 within a certain range. In this respect, hydrogen bonds (for example, hydrogen bonds formed between water-absorbing fibers, between thermoplastic resin fibers, between water-absorbing fibers and thermoplastic resin fibers, etc.) contribute to maintaining the bulk of the reservoir layer 41. The hydrogen bond is formed, for example, between an oxygen atom of a thermoplastic resin fiber (for example, an oxygen atom such as a carboxyl group, an acyl group, or an ether bond) and a hydrogen atom of cellulose (for example, a hydrogen atom of a hydroxyl group). . The hydrogen bond is cut by the liquid absorbed in the storage layer 41.

The maximum tensile strength during drying of the reservoir 41 (maximum tensile strength at a basis weight of 200 g / m ² ) is preferably 3 to 36 N / 25 mm, more preferably 8 to 20 N / 25 mm. The strength (maximum tensile strength at a basis weight of 200 g / m ² ) is preferably 2 to 32 N / 25 mm, more preferably 5 to 15 N / 25 mm. Thereby, the storage layer 41 can hold | maintain sufficient intensity | strength through before and after liquid absorption (namely, not only at the time of drying but at the time of wetness). The mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer 41 is 1/9 or more is a necessary condition for realizing the strength of the reservoir layer 41. Note that “N / 25 mm” means the maximum tensile strength (N) per 25 mm width in the planar direction of the reservoir layer 41, and the plane direction of the reservoir layer 41 is, for example, the transport direction when the reservoir layer 41 is manufactured. (MD direction), a direction orthogonal to the MD direction (CD direction), and the like can be mentioned, and the MD direction is preferable.

The measurement of the maximum tensile strength at the time of drying of the reservoir layer 41 is performed as follows.
A sample piece (length 150 mm x width 25 mm) at standard time (temperature 20 ° C., humidity 60%) is attached to a tensile tester (manufactured by Shimadzu Corporation, AG-1kNI) at a grip interval of 100 mm, and pulled at 100 mm / min. A load (maximum point load) is applied until the sample piece is cut at a speed, and the maximum tensile strength (N / 25 mm) is measured. “N / 25 mm” means the maximum tensile strength (N) per 25 mm width in the length direction of the sample piece.

The measurement of the maximum tensile strength when the reservoir 41 is wet is performed as follows.
After dipping a sample piece (length 150 mm x width 25 mm) in ion-exchanged water until it sinks under its own weight, or after submerging the sample piece in water for 1 hour or more, the maximum tensile strength during drying is The tensile strength (N / 25 mm) is measured. “N / 25 mm” means the maximum tensile strength (N) per 25 mm width in the length direction of the sample piece.

  Regarding the measurement of the maximum tensile strength at the time of dryness and wetness, the measurement conditions described in ISO 9073-3 or JIS L 1913: 2010 6.3 are adopted for the measurement conditions not particularly specified above.

  The difference between the maximum tensile strength when dry and the maximum tensile strength when wet (the maximum tensile strength when dry-the maximum tensile strength when wet) of the storage layer 41 is preferably 1 to 5 N / 25 mm, more preferably 2 to 4 N / 25 mm. is there. Thereby, the storage layer 41 has sufficient strength to maintain an integrated structure with the coating layer 43a through before and after liquid absorption (that is, not only when dry but also when wet). The mass ratio of the thermoplastic resin fibers to the water-absorbing fibers in the reservoir layer 41 is 1/9 or more is a necessary condition for realizing the strength of the reservoir layer 41. In addition, since the hydrogen bond formed at the time of drying is cut | disconnected at the time of wetness, the difference of the maximum tensile strength at the time of drying and the maximum tensile strength at the time of wetness becomes a parameter | index of the amount of hydrogen bonds.

  Examples of the cellulosic water-absorbing fibers contained in the reservoir layer 41 include wood pulp obtained from softwood or hardwood as a raw material (for example, mechanical pulp such as groundwood pulp, refiner ground pulp, thermomechanical pulp, chemithermomechanical pulp; Kraft pulp, sulfide pulp, alkaline pulp and other chemical pulp; semi-chemical pulp, etc.); mercerized pulp or crosslinked pulp obtained by chemically treating wood pulp; bagasse, kenaf, bamboo, hemp, cotton (for example, cotton linter) Non-wood pulp such as: Recycled fiber such as rayon fiber.

  The thermoplastic resin fiber contained in the reservoir layer 41 is not particularly limited as long as it is a thermoplastic resin fiber containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride or a mixture thereof as a monomer component, strength, From the viewpoint of hydrogen bondability, heat-fusibility, etc., it can be selected as appropriate.

  Examples of the thermoplastic resin fiber contained in the storage layer 41 include a modified polyolefin graft-polymerized with a vinyl monomer containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride, or a mixture thereof, or the modified polyolefin and other resins. And a core-sheath type composite fiber using a resin having a melting point higher than that of the modified polyolefin as a core component.

  Examples of the unsaturated carboxylic acid or unsaturated carboxylic acid anhydride include maleic acid or derivatives thereof, maleic anhydride or derivatives thereof, fumaric acid or derivatives thereof, unsaturated derivatives of malonic acid, and unsaturated derivatives of succinic acid. Examples of other vinyl monomers include general-purpose monomers having radical polymerizability, for example, styrenes such as styrene and α-methylstyrene; methyl (meth) acrylate, ethyl (meth) acrylate, ( And (meth) acrylic acid esters such as 2-hydroxyethyl (meth) acrylate and dimethylaminoethyl (meth) acrylate. Examples of maleic acid derivatives or maleic anhydride derivatives include citraconic acid, citraconic anhydride, pyrocynconic anhydride, and the like, and examples of fumaric acid derivatives or malonic acid unsaturated derivatives include 3-butene- Examples include 1,1-dicarboxylic acid, benzylidenemalonic acid, isopropylidenemalonic acid, and the like. Examples of the unsaturated derivative of succinic acid include itaconic acid and itaconic anhydride.

  As the backbone polymer of modified polyolefin, linear low density polyethylene (LLDPE), low density polyethylene (LDPE), medium density polyethylene (MDPE), high density polyethylene (HDPE), polypropylene, polybutylene, and copolymers based on these (For example, ethylene-vinyl acetate copolymer (EVA), ethylene-ethyl acrylate copolymer (EEA), ethylene-acrylic acid copolymer (EAA), ionomer resin, etc.).

  For example, graft polymerization of vinyl monomer to the trunk polymer uses a radical initiator, mixes unsaturated carboxylic acid or unsaturated carboxylic acid anhydride and vinyl monomer into polyolefin, and introduces side chains made of random copolymer. And a conventional method such as a method of sequentially polymerizing different monomers and introducing a side chain comprising a block copolymer.

  The sheath component may be a modified polyolefin alone or a mixed polymer of the modified polyolefin and another resin. The other resin is preferably a polyolefin, and more preferably the same type of polyolefin as the backbone polymer of the modified polyolefin. For example, when the trunk polymer is polyethylene, the other resin is also preferably polyethylene.

  The resin used as the core component is not particularly limited as long as the resin has a higher melting point than the modified polyolefin. For example, polyamides such as 6-nylon and 6,6-nylon; polyethylene terephthalate (PET), polytrimethylene terephthalate (PTT), polybutylene terephthalate (PBT), polylactic acid, polyglycolic acid and other linear or branched polyesters having up to 20 carbon atoms such as polyhydroxyalkanoic acid and copolymers mainly composed of these Or a copolymerized polyester obtained by copolymerizing a small amount of other components with alkylene terephthalate as a main component. PET is preferable from the viewpoint of having high resilience and high cushioning properties, and from the economical viewpoint of being industrially inexpensive.

  Spinning is possible if the composite ratio of the sheath component to the core component is in the range of 10/90 to 90/10, but is preferably 30/70 to 70/30. If the sheath component ratio decreases too much, the heat-fusibility decreases, and if it increases too much, the spinnability decreases.

  The thermoplastic resin fibers contained in the reservoir layer 41 include antioxidants, light stabilizers, ultraviolet absorbers, neutralizers, nucleating agents, epoxy stabilizers, lubricants, antibacterial agents, flame retardants, antistatic agents, You may add additives, such as a pigment and a plasticizer, as needed. The thermoplastic resin fiber is preferably hydrophilized with a surfactant, a hydrophilic agent or the like.

  Although the fiber length of the thermoplastic resin fiber contained in the storage layer 41 is not particularly limited, it is preferably 3 to 70 mm, more preferably 5 to 20 mm when mixed with pulp by the airlaid system. Below this range, the number of junctions with the water-absorbing fibers decreases, so that sufficient strength cannot be imparted to the reservoir 41. On the other hand, if it exceeds this range, the defibrating property is remarkably lowered and a large number of undefibrated states are generated, so that formation unevenness occurs and the uniformity of the reservoir 41 is lowered. The fineness of the thermoplastic resin fiber is preferably 0.5 to 10 dtex, more preferably 1.5 to 5 dtex. When the fineness is less than 0.5 dtex, the defibration property is lowered, and when it exceeds 10 dtex, the number of fibers is reduced and the strength is lowered.

  A three-dimensional crimped shape may be imparted to the thermoplastic resin fibers contained in the reservoir layer 41. Thereby, even when the fiber orientation is in the plane direction, the buckling strength of the fiber works in the thickness direction, so that it is difficult to be crushed even if an external pressure is applied. Examples of the three-dimensional crimped shape include a zigzag shape, an Ω shape, and a spiral shape. Examples of the method for imparting the three-dimensional crimped shape include mechanical crimping and shape provision by heat shrinkage. Mechanical crimping can be controlled by the difference in peripheral speed of the line speed, heat, pressurization, etc. for continuous linear fibers after spinning, and the greater the number of crimps per unit length, the greater the resistance to external pressure. The buckling strength is increased. The number of crimps is usually 5 to 35 pieces / inch, preferably 15 to 30 pieces / inch. In shape imparting by heat shrinkage, for example, by applying heat to fibers made of two or more resins having different melting points, it is possible to perform three-dimensional crimping by utilizing the difference in heat shrinkage caused by the melting point difference. is there. Examples of the shape of the fiber cross section include an eccentric type and a side-by-side type of a core-sheath type composite fiber. The thermal contraction rate of such a fiber is preferably 5 to 90%, more preferably 10 to 80%.

The thickness, basis weight, and the like of the reservoir layer 41 can be appropriately adjusted according to characteristics (for example, absorbency, strength, lightness, etc.) that the diaper 1 should have. The thickness of the reservoir layer 41 is usually 0.1 to 15 mm, preferably 1 to 10 mm, more preferably 2 to 5 mm, and the basis weight is usually 20 to 1000 g / m ² , preferably 40 to 900 g / m ² , More preferably, it is 100-400 g / m < ² >. When the basis weight is less than 40 g / m ² , the fiber amount of the thermoplastic resin fibers becomes insufficient, and the strength of the reservoir layer 41 (particularly the strength when wet) may not be maintained, but exceeds 900 g / m ² . Then, the amount of the thermoplastic resin fiber becomes excessive, and the rigidity of the storage layer 41 may be too high. In addition, the thickness, basic weight, etc. of the storage layer 41 may be constant over the whole, and may differ partially.

  The storage layer 41 may be integrated with the top sheet 2 by a through hole that penetrates the top sheet 2 and the storage layer 41. Thereby, the absorptivity / accommodability of a liquid (for example, menstrual blood) having a high viscosity is improved. The opening ratio of the through holes penetrating the top sheet 2 and the storage layer 41 (ratio of the total area of the through holes to the area of the top sheet 2) is preferably 0.1 to 20%, more preferably 1 to 10%. The diameter of the through holes is preferably 0.1 to 5 mm, more preferably 0.5 to 3 mm, and the interval between the through holes is preferably 0.2 to 30 mm, and more preferably 5 to 20 mm.

  The thermoplastic resin fibers contained in the reservoir layer 41 may be colored with a pigment or the like. Thereby, it is easy to visually check whether the water-absorbing fibers and the thermoplastic resin fibers are uniformly dispersed. In addition, the color of the absorbed liquid can be masked. For example, when the absorbed liquid is urine, it is colored blue, and when it is menstrual blood, it is colored green so that the wearer can feel clean.

  The storage layer 41 may contain silver, copper, zinc, silica, activated carbon, an aluminosilicate compound, zeolite, or the like in order to impart a desired function. Thereby, functions, such as a deodorizing property, antibacterial property, and an endothermic effect, can be provided.

  The storage layer 41 is preferably obtained by injecting high-pressure steam into a mixed material containing water-absorbing fibers and thermoplastic resin fibers to increase the density. The density of the reservoir 41 can be adjusted to a desired range by increasing the density using high-pressure steam injection. When high-pressure water vapor is injected into the mixed material, the water vapor penetrates into the mixed material and forms hydrogen bonds (for example, between water-absorbing fibers, between thermoplastic resin fibers, between water-absorbing fibers and thermoplastic resin fibers, etc.). (Hydrogen bonds) are broken, and the mixed material is softened. Therefore, the pressure required for densification is reduced, and the softened mixed material can be easily adjusted in density. When the density-adjusted mixed material is dried and hydrogen bonds are re-formed, the elastic recovery (increase in volume) of the fibers is suppressed, and the density of the storage layer 41 is maintained in a certain range.

  Densification by jetting high-pressure steam is particularly suitable when an unsaturated carboxylic acid anhydride (for example, maleic anhydride or a derivative thereof) is contained as a monomer component in the thermoplastic resin fiber. When the unsaturated carboxylic acid anhydride group contained in the thermoplastic resin fiber reacts with water vapor to form an unsaturated carboxylic acid group, the number of oxygen atoms capable of forming hydrogen bonds increases, so the density-adjusted fiber elasticity Recovery (increase in bulk) is effectively suppressed.

Densification by injection of high-pressure steam is performed, for example, after bonding thermoplastic resin fibers with water-absorbing fibers. The temperature, vapor pressure and the like of the high-pressure steam are appropriately adjusted according to the required fiber density range and the like. The temperature of the high-pressure steam is preferably less than the melting point of the thermoplastic resin fiber (for example, when the thermoplastic resin fiber is a core-sheath type composite fiber, the melting point of the sheath component). High-pressure steam is preferably injected per unit surface area ^{0.03kg / m 2 ~1.23kg / m 2} . The vapor pressure of the high-pressure steam is usually from 0.1 to 2 Mpa, preferably from 0.3 to 0.8 Mpa.

When the densification is performed by jetting high-pressure steam, the basis weight of the reservoir layer 41 is preferably 40 to 900 g / m ² , and more preferably 100 to 400 g / m ² . If the fiber basis weight is less than 40 g / m ² , the amount of fibers is too small, so that it is difficult to increase the density by jetting high-pressure steam. On the other hand, if the fiber basis weight exceeds 900 g / m ² , the amount of fibers is too large. It becomes difficult to penetrate inside.

  By injecting the high-pressure steam, the collar portion and the groove portion can be formed on the surface of the storage layer 41. The number, interval, and the like of the flange portion and the groove portion vary depending on the number, pitch, and the like of nozzles that inject high-pressure steam. In addition, the part into which high-pressure steam is injected becomes a groove part. The collar portion and the groove portion may be formed on the surface of the storage layer 41 on the top sheet 2 side, or may be formed on the surface of the storage layer 41 on the back sheet 3 side.

  The eaves part and the groove part can be formed so as to extend in the longitudinal direction (Y-axis direction) of the reservoir 41 and to be alternately arranged in the width direction (X-axis direction) of the reservoir 41. The eaves part and the groove part may extend continuously in the longitudinal direction (Y-axis direction) of the storage layer 41, or may extend intermittently in a state where a part thereof is missing. For example, the collar part and the groove part may extend intermittently so that the part lacking the collar part and the groove part has a rectangular shape in plan view, a staggered shape in plan view, or the like.

  Further, the flange and the groove can be formed so as to extend in the width direction (X-axis direction) of the storage layer 41 and to be alternately arranged in the longitudinal direction (Y-axis direction) of the storage layer 41. The eaves part and the groove part may extend continuously in the width direction (X-axis direction) of the storage layer 41, or may extend intermittently in a state of lacking a part thereof. For example, the collar part or the groove part may extend intermittently so that the part lacking the collar part or the groove part has a rectangular shape in plan view, a staggered shape in plan view, or the like. When a plurality of ridges and grooves extending in the width direction (X-axis direction) of the storage layer 41 are formed on the top sheet 2 side surface or the back sheet 3 side surface of the storage layer 41, the width of the storage layer 41 Even if a force is applied in the direction, the reservoir 41 is not easily twisted, and the reservoir 41 is easily deformed into a curved shape along the shape of the wearer's body. Therefore, it is difficult for the wearer to feel uncomfortable.

  The shape of the buttocks is not particularly limited. For example, the top part and side surface of the collar part are curved surfaces, and the cross-sectional shape of the collar part is a substantially inverted U-shape toward the top sheet or the back sheet. The cross-sectional shape of the collar portion can be changed as appropriate, and may be, for example, a dome shape, a trapezoidal shape, a triangular shape, or an Ω-shaped square shape. Even when a force is applied to the reservoir 41 and the buttock is crushed, the width of the ridge is preferably narrowed from the bottom toward the top so that the space of the groove is maintained.

  From the viewpoint of liquid migration from the top sheet 2, the width of the collar portion is preferably 0.5 to 10 mm, and more preferably 2 to 5 mm. From the same viewpoint, the width of the groove is preferably 0.1 to 10 mm, and more preferably 1 to 5 mm.

  When a plurality of flanges are formed, the widths of the flanges may be substantially the same or different. For example, although the width of one collar is different from the width of another collar, a plurality of collars can be formed so as to be substantially the same as the width of another collar. The same applies when a plurality of grooves are formed.

  The high-pressure steam may be injected over the entire mixed material or may be injected over a part thereof. Moreover, you may change the temperature of high-pressure steam, vapor pressure, etc. which are injected for every part of mixed material. The fiber density distribution of the reservoir layer 41 can be changed by partially injecting high-pressure steam into the mixed material or by changing the temperature, vapor pressure, etc. of the high-pressure steam to be injected for each part of the mixed material. .

  The high-pressure steam may be injected while pressing the mixed material, or may be injected without pressing. The fiber density distribution of the reservoir layer 41 can be changed by injecting high-pressure steam while pressing a part of the mixed material and injecting high-pressure steam without pressing the other part. For example, when high-pressure steam is sprayed onto the mixed material while passing between mesh conveyor belts that are partially open, high-pressure steam is directly applied to the mesh conveyor belt without being pressed at the opening of the mesh conveyor belt, and the mesh conveyor belt is not open. Then, since high-pressure steam is applied while being pressed, the fiber density distribution can be changed.

In the case of increasing the density by jetting high-pressure steam, it is advantageous in the following points as compared with other methods. When the mixed material is densified by press roll molding, high compression is required to provide a bonding force between fibers that exceeds the repulsive force of the fibers. Moreover, even if compressed once by high compression, a fiber will elastically recover and a bulk will return. On the other hand, when the density of the mixed material is increased by combining a press roll and water spray, if the basis weight is 100 g / m ² or less, moisture can penetrate into the mixed material, but the basis weight is 100 g / m ^2. If it exceeds m ² , it becomes difficult to permeate moisture into the mixed material, and hydrogen bonds cannot be formed inside the mixed material. Moreover, if excessive moisture is given, it becomes possible to allow moisture to penetrate into the mixed material. In this case, however, an excessive amount of heat and time are required to evaporate the moisture, resulting in a decrease in productivity. On the other hand, when the density is increased by jetting high-pressure steam, the steam penetrates into the mixed material, and hydrogen bonds (for example, between water-absorbing fibers, between thermoplastic resin fibers, and between water-absorbing fibers and thermoplastic resin fibers). The hydrogen bond formed between them is broken, and the mixed material is softened. Therefore, the pressure required for densification is reduced, and the density of the softened mixed material can be easily adjusted. Further, the water vapor easily evaporates and the time required for drying is short, so that productivity is improved.

The absorptive core 42 contains a super absorbent polymer material as an absorptive material. The basis weight of the superabsorbent polymer material contained in the absorbent core 42 is usually 10 to 1000 g / m ² , preferably 100 to 500 g / m ² , and more preferably 150 to 350 g / m ² . Examples of the superabsorbent polymer material include starch-based, cellulose-based, and synthetic polymer-based superabsorbent polymer materials. Examples of the starch-based or cellulose-based superabsorbent polymer material include starch-acrylic acid (salt) graft copolymer, saponified starch-acrylonitrile copolymer, and a crosslinked product of sodium carboxymethyl cellulose. Examples of polymer superabsorbent polymer materials include polyacrylate, polysulfonate, maleic anhydride, polyacrylamide, polyvinyl alcohol, polyethylene oxide, polyaspartate, and polyglutamic acid. High water-absorbing polymer materials such as salt-based, polyalginate-based, starch-based, and cellulose-based materials can be mentioned. Of these, polyacrylate-based (particularly sodium polyacrylate-based) highly water-absorbing polymer materials are preferable. . Examples of the shape of the superabsorbent polymer material include particulates, fibers, scales, and the like, and in the case of particulates, the particle size is preferably 50 to 1000 μm, more preferably 100 to 600 μm. is there. The measurement of the particle size of the superabsorbent polymer particles is carried out according to the screening test method described in JIS R 6002: 1998.

  The absorbent core 42 may contain an absorbent material other than the superabsorbent polymer material. Examples of the absorbent material other than the superabsorbent polymer material include hydrophilic fibers. Examples of hydrophilic fibers include wood pulp obtained from coniferous or hardwood as a raw material (for example, groundwood pulp, refiner ground pulp, Mechanical pulp such as thermomechanical pulp and chemithermomechanical pulp; chemical pulp such as kraft pulp, sulfide pulp and alkali pulp; semi-chemical pulp etc.); mercerized pulp or crosslinked pulp obtained by subjecting wood pulp to chemical treatment; bagasse Non-wood pulp such as kenaf, bamboo, hemp, and cotton (for example, cotton linter); regenerated cellulose such as rayon and fibrillar rayon; semisynthetic cellulose such as acetate and triacetate, etc. Among these, the cost is low, Pulverized pulp is preferred because it is easy to mold. Arbitrariness. When the absorbent core 42 contains an absorbent material other than the superabsorbent polymer material, the mass ratio of the superabsorbent polymer material to the other absorbent material in the absorbent core 42 (content of superabsorbent polymer material) : Content of other absorbent material) is usually 0.5: 9.5 to 9.5: 0.5, preferably 2: 8 to 8: 2, more preferably 3: 7 to 7: 3. is there.

  In addition to the absorbent material, the absorbent core 42 includes an antioxidant, a light stabilizer, an ultraviolet absorber, a neutralizer, a nucleating agent, an epoxy stabilizer, a lubricant, an antibacterial agent, a flame retardant, an antistatic agent, and a pigment. An additive such as a plasticizer may be contained as necessary. For example, the absorptive core 42 can exhibit functions such as deodorizing property, antibacterial property, and endothermic effect by containing silver, copper, zinc, silica, activated carbon, an aluminosilicate compound, zeolite, and the like.

  The core wraps 43a and 43 are an example of a coating layer that covers the absorbent core, the core wrap 43a covers the surface of the absorbent core 42 on the storage layer 41 side, and the core wrap 43b is the storage layer 41 side of the absorbent core 42. Cover the surface opposite to.

  The core wraps 43a and 43b contain cellulosic water-absorbing fibers. Specific examples of the cellulose water-absorbing fibers contained in the core wraps 43a and 43b include the same specific examples as the cellulose water-absorbing fibers contained in the reservoir layer 41. The cellulose water-absorbing fibers contained in the core wraps 43a and 43b and the cellulose water-absorbing fibers contained in the reservoir layer 41 may be the same or different. The core wraps 43a and 43b are not particularly limited as long as they have liquid permeability and absorbent core retention, and examples thereof include non-woven fabrics and woven fabrics. Non-woven fabrics are preferred, and wet methods using pulverized pulp as the main material. More preferred is a tissue molded with As a nonwoven fabric, the same specific example as the top sheet 2 is mentioned. By covering with the core wraps 43a and 43b, it is possible to prevent the absorbent core 42 from collapsing, improve the cushioning property of the absorbent body 4, improve the concealability of the absorbent body 4, reduce the rewet back of the absorbent body 4, and the like.

The basis weight of the cellulosic water-absorbing fibers contained in the core wraps 43a and 43b is usually 1 to 50 g / m ² , preferably 5 to 30 g / m ² , and more preferably 10 to 20 g / m ² . If the basis weight is less than 1 g / m ² , the amount of fibers is too small, so that it is difficult to form an integrated part. On the other hand, if it exceeds 50 g / m ² , the amount of fibers is too large, and the rigidity of the integrated part is too high. May become excessively high. The core wraps 43a and 43b may contain water absorbent fibers other than the cellulosic water absorbent fibers. When the core wraps 43a and 43b contain water absorbent fibers other than the cellulosic water absorbent fibers, the mass ratio of the cellulosic water absorbent fibers and the other water absorbent fibers in the core wraps 43a and 43b (content of the cellulosic water absorbent fibers). : Content of other water-absorbing fibers) is usually 0.5: 9.5 to 9.5: 0.5, preferably 2: 8 to 8: 2, more preferably 3: 7 to 7: 3. is there.

  In the present embodiment, the core wraps 43a and 43b are separate members, but may be a single continuous member. In the present embodiment, a part of the surface of the absorbent core 42 is not covered with the core wraps 43a and 43b, but the entire surface of the absorbent core 42 may be covered with the core wraps 43a and 43b. .

  As shown in FIGS. 3 and 4, when the absorbent body 4 is viewed in plan from the top sheet 2 side, a large number of substantially circular integrated portions 44 are formed on substantially the entire surface of the storage layer 41 on the top sheet 2 side. It is formed in a staggered pattern. The formation pattern of the integrated portion 44 can be changed as appropriate. Examples of the formation pattern other than the present embodiment (pattern when the absorber 4 is viewed in plan view from the top sheet 2 side) are, for example, linear, curved, annular Etc.

  The integrated part 44 in this embodiment is a recessed part formed by the heat embossing process, as shown in FIG. In the heat embossing process, among the surface of the storage layer 41, a large number of parts that are separated from each other are compressed and heated in the thickness direction of the absorber 4 until the core wrap 43a is reached. Thereby, the integrated part 44 which unifies the storage layer 41 and the core wrap 43a is formed as a pressing part which has the depth which reaches the core wrap 43a.

  The heat embossing process is performed by, for example, a method of embossing the storage layer 41 and the core wrap 43a between an embossing roll having a patterned convex portion on the outer peripheral surface and a flat roll having a smooth outer peripheral surface. Is called. In this method, heating at the time of compression is possible by heating the embossing roll and / or the flat roll. Examples of the emboss pattern of the emboss roll include a lattice pattern, a staggered pattern, and a wavy pattern. Regarding the convex portion of embossing, the tip diameter is usually from 0.1 to 5 mm, preferably from 1 to 2 mm, the height is usually from 0.1 to 15 mm, preferably from 2 to 5 mm, and the pitch (that is, the interval between the compressed parts). ) Is usually 1 to 30 mm, preferably 4 to 12 mm with respect to the longitudinal direction of the absorbent body 4, and is usually 1 to 30 mm, preferably 4 to 15 mm with respect to the width direction. The heating temperature in the embossing treatment is usually 80 to 160 ° C., preferably 120 to 160 ° C., the pressure is usually 10 to 3000 N / mm, preferably 50 to 500 N / mm, and the treatment time is usually 0.0001 to 5 Second, preferably 0.005 to 2 seconds.

  By the heat embossing process, the thermoplastic resin fibers contained in the reservoir layer 41 are thermally fused with the cellulosic water-absorbing fibers contained in the core wrap 43a, so that the reservoir layer 41 and the core wrap 43a are integrated. Thereby, the interfacial peel strength between the reservoir layer 41 and the core wrap 43a increases.

  The heat embossing process is an example of a method for forming an integrated part that integrates the storage layer 41 and the core wrap 43a. Examples of the forming method other than the heat embossing process include ultrasonic embossing and heating fluid ejection process. Examples of the heating fluid injection process include a high-pressure steam injection process and a heated air injection process.

  In the heating fluid ejection process, an integrated portion that integrates the reservoir 41 and the core wrap 43a is formed by ejecting the heating fluid to the reservoir 41. Examples of the heating fluid include high-pressure steam and heated air. In the ejection of the heating fluid, for example, a plurality of regions extending in the longitudinal direction of the absorber 4 and arranged in the width direction on the surface of the storage layer 41 are compressed and heated in the thickness direction of the absorber 4. Of the reservoir 41, the portion where the heated fluid is ejected becomes a groove portion, and the portion where the heated fluid is not ejected becomes a flange portion. The integrated part that integrates the reservoir layer 41 and the core wrap 43a is formed on the contact surface between the groove and the core wrap 43a. The number, interval, and the like of the groove portions and the flange portions vary depending on the number of nozzles that eject the heated fluid, the pitch, and the like.

The temperature, pressure, and the like of the heating fluid are adjusted as appropriate according to the melting point of the thermoplastic resin contained in the storage layer 41. The temperature of the heating fluid is preferably equal to or higher than the melting point of the thermoplastic resin fibers contained in the reservoir layer 41 (for example, when the thermoplastic resin fibers are core-sheath type composite fibers, the melting point of the sheath component). If the heating fluid is high-pressure steam, it is preferable to injection by unit surface area per ^{0.03kg / m 2 ~1.23kg / m 2} , the vapor pressure of the high pressure steam, typically 0.1 to 2 MPa, preferably 0. 3 to 0.8 Mpa.

  The interfacial peel strength during drying of the reservoir layer 41 and the core wrap 43a is preferably 1.75 to 4.23 N / 25 mm, and the wet interfacial peel strength is preferably 1.05 to 2.63 N / 25 mm. Note that “N / 25 mm” means the interfacial peel strength (N) per width of 25 mm in the planar direction of the absorbent body 4, and the planar direction of the absorbent body 4 is, for example, the transport direction during manufacture of the absorbent body 4 (MD direction), a direction orthogonal to the MD direction (CD direction), and the like can be mentioned, and the MD direction is preferable.

The measurement of the interfacial peel strength at the time of drying is performed as follows.
A sample piece (length 40 mm x width 25 mm) at standard time (temperature 20 ° C., humidity 60%) is held by a tensile tester (Shimadzu Corporation, AG-1kNI) at an interval of 20 mm, and the reservoir 41 is placed on the lower side. The core wrap 43a is attached to the grip, and measurement is performed by applying a load (maximum point load) until the sample piece completely peels off at a pulling speed of 100 mm / min. In this case, “N / 25 mm” means the interfacial peel strength (N) per 25 mm width in the length direction of the sample piece.

The measurement of the interfacial peel strength when wet is performed as follows.
After the sample piece (length 40 mm × width 25 mm) is immersed in ion-exchanged water until it sinks under its own weight, or after the sample piece has been submerged in water for 1 hour or longer, the measurement is performed in the same manner as in drying. In this case, “N / 25 mm” means the interfacial peel strength (N) per 25 mm width in the length direction of the sample piece.

  Regarding the measurement of the interfacial peel strength when dry and wet, the measurement conditions described in ISO 9073-3 or JIS L 1913 6.3 were adopted as the measurement conditions not particularly specified above.

In the present embodiment, among a large number of integrated portions 44 formed in a staggered pattern on substantially the entire surface of the storage layer 41 on the topsheet 2 side, usually 0.5 to 50 pieces / cm ² , preferably Sample pieces cut out from the absorber 4 so as to include 1 to 30 pieces / cm ² , more preferably 2 to 20 pieces / cm ² , are used for measurement of the interfacial peel strength. Similarly, when the formation pattern of the integrated part is different from that of the present embodiment, the sample piece cut out from the absorber so as to include the integrated part is used for the measurement of the interfacial peel strength. When the integrated part includes a part extending in the longitudinal direction of the absorbent body, it is preferable to use a sample piece including a part extending in the longitudinal direction of the absorbent body. Moreover, it is preferable that the length direction of a sample piece corresponds with the extension direction of an integrated part. For example, the absorbent body is cut along both sides of the integrated portion extending in the longitudinal direction, and by cutting perpendicularly to the integrated portion extending in the longitudinal direction, the length direction becomes the integrated portion. It is possible to produce a sample piece that coincides with the extending direction.

  As shown in FIGS. 1 to 3, the diaper 1 includes a liquid-impermeable cover sheet 6, a liquid-impermeable leak-proof cuff 7 a and 7 b, a liquid, in addition to the top sheet 2, the back sheet 3 and the absorber 4. An impermeable leak-proof sheet 8, elastic members 91, 92, 93, 94 and the like are provided. Hereinafter, these members will be described.

<Cover sheet>
As shown in FIGS. 1 to 3, a liquid-impermeable cover sheet 6 is provided on the skin side surface of the top sheet 2. As shown in FIGS. 1 to 3, an opening 61 is formed at substantially the center of the cover sheet 6, and a part of the top sheet 2 (a part of the arrangement region of the absorber 4) It is exposed from the opening 61 and constitutes the skin side surface of the diaper 1 together with the cover sheet 6.

  The cover sheet 6 is a liquid-impermeable sheet. Examples of the liquid-impermeable sheet include a waterproofed nonwoven fabric (for example, a point bond nonwoven fabric, a spunbond nonwoven fabric, a spunlace nonwoven fabric, etc.), a synthetic resin (for example, , Polyethylene, polypropylene, polyethylene terephthalate, etc.) film, a composite sheet of a nonwoven fabric and a synthetic resin film, and the like.

<Leak-proof cuff>
As shown in FIGS. 1 to 3, on both sides of the opening 61 of the cover sheet 6, leak-proof cuffs 7 a and 7 b made of a liquid-impermeable sheet are provided. One end of each of the leak-proof cuffs 7 a and 7 b is a fixed end sandwiched between the top sheet 2 and the cover sheet 6, and the other end is exposed from the opening 61 of the cover sheet 6. The free end to do. Elastic portions 71a and 71b extending in the longitudinal direction Y are provided at the free ends of the leak-proof cuffs 7a and 7b, and the leak-proof cuffs 7a and 7b stand up toward the wearer's skin.

<Leak-proof sheet>
As shown in FIGS. 2 and 3, a liquid-impermeable leak-proof sheet 8 is provided between the back sheet 3 and the absorber 4. The leak-proof sheet 8 is a liquid-impermeable sheet, and examples of the liquid-impermeable sheet include waterproof nonwoven fabrics (for example, point bond nonwoven fabrics, spunbond nonwoven fabrics, spunlace nonwoven fabrics, etc.), synthetic resins ( For example, polyethylene, polypropylene, polyethylene terephthalate, etc.) film, a composite sheet of a nonwoven fabric and a synthetic resin film, and the like can be mentioned.

<Elastic member>
As shown in FIGS. 1 to 3, elastic members 91, 92, 93, and 94 are provided between the back sheet 3 and the cover sheet 6 that are hourglass shapes having substantially the same dimensions. In FIG. 1, some of the elastic members 91, 92, 93, and 94 are omitted.

  As shown in FIG. 1, a waist gather is formed in the waist opening by the elastic contraction force of the elastic members 91 and 92, and a leg gather (leg) is formed in the leg opening by the elastic contraction force of the elastic members 93 and 94. Side cuff) is formed. Leakage of liquid excretion from the leg opening is prevented by the leg gathers.

  As the elastic members 91 and 92, for example, a strand-like or string-like elastic body having a thickness of about 310 to 940 dtex can be used. As the elastic members 93 and 94, for example, a strand having a thickness of about 470 to 940 dtex can be used. A string-like or string-like elastic body can be used. As the elastic members 91, 92, 93, 94, elastic fiber nonwoven fabrics having elasticity or the like may be used.

  As shown in FIGS. 2 and 3, the elastic members 91 and 92 are attached to the front surface portion 11 and the rear surface portion 13 such that the elastic members 91 and 92 can be contracted in the expanded state in the lateral direction X and separated in the longitudinal direction Y. ing. As shown in FIGS. 2 and 3, the elastic member 93 includes portions 93 a and 93 b extending along both side portions 121 a and 121 b of the intermediate portion 12, and a portion 93 c extending in the lateral direction X and connecting the portions 93 a and 93 b. have. 2 and 3, the elastic member 94 includes portions 94a and 94b extending along both side portions 121a and 121b of the intermediate portion 12, and a portion 94c extending in the lateral direction X and connecting the portions 94a and 94b. have. Since the absorbent body 4 extends from the front surface portion 11 to the rear surface portion 13 through the intermediate portion 12, the absorbent body 4 is pressed against the wearer's skin side by the contraction force of the elastic members 91, 92, 93, 94. Leakage of the liquid excrement of the wearer is prevented.

  The diaper 1 is worn so that the top sheet 2 and the cover sheet 6 are positioned on the inner side (the wearer's skin side) and the back sheet 3 is positioned on the outer side (the wearer's clothing side). However, it is not necessary for the wearer to wear clothes. The liquid excrement of the wearer penetrates the absorbent body 4 through the top sheet 2 exposed from the opening 61 of the cover sheet 6 and is absorbed and held by the absorbent body 4. Leakage of the liquid excretion absorbed and held by the absorber 4 is prevented by the back sheet 3 and the leak-proof sheet 6. Examples of liquid excreta to be absorbed include urine, menstrual blood, and fallen products, but are usually mainly urine.

Various changes can be made in the diaper 1. Hereinafter, a modified example of the diaper 1 will be described.
<Modification A>
In the modified example A of the diaper 1, instead of the integrated portion 44, an integrated portion 44 ′ (not shown) that integrates the reservoir layer 41, the core wrap 43a, and the core wrap 43b is formed. The integrated part 44 ′ is a recessed part formed by heat embossing treatment, like the integrated part 44. In the heat embossing process, a large number of parts separated from each other in the surface of the storage layer 41 are compressed and heated in the thickness direction of the absorber 4 until reaching the core wrap 43b. Thereby, 44 A of integrated parts which integrate the storage layer 41, the core wrap 43a, and the core wrap 43b are formed as a pressing part which has the depth which reaches the core wrap 43b.

Hereinafter, based on FIG. 5, one Embodiment of the manufacturing method of the absorber of this invention is described.
[First step]
The carrier sheet 150 traveling in the machine direction (MD direction) includes an absorbent core containing superabsorbent polymer particles, an upper core wrap covering the upper surface of the absorbent core, and a lower core wrap covering the lower surface of the absorbent core. Are stacked intermittently. The SAP particles contained in the absorbent core are fixed between the upper core wrap and the lower core wrap by a hot melt adhesive (HMA) applied to the lower surface of the upper core wrap and the upper surface of the lower core wrap. The adhesive is applied in a pattern such as a dot, a spiral, or a stripe. As the hot melt adhesive, for example, styrene-ethylene-butadiene-styrene (SEBS), styrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS) and the like, or linear Pressure-sensitive adhesives or heat-sensitive adhesives mainly composed of olefins such as low density polyethylene; water-soluble polymers (for example, polyvinyl alcohol, carboxymethyl cellulose, gelatin, etc.) or water-swellable polymers (for example, polyvinyl acetate, poly And water sensitive adhesives such as sodium acrylate). Examples of the method for applying the adhesive include spiral coating, coater coating, curtain coater coating, and summit gun coating.

  On the peripheral surface 151a of the suction drum 151 rotating in the MD direction, recesses 153 are formed at a required pitch in the circumferential direction as a mold for filling the fiber material. When the suction drum 151 rotates and the recess 153 enters the fiber material supply unit 152, the suction unit 156 acts on the recess, and the fiber material supplied from the fiber material supply unit 152 is vacuum sucked into the recess 153.

  The hooded fiber material supply unit 152 is formed so as to cover the suction drum 151, and the fiber material supply unit 152 includes a cellulosic water-absorbing fiber, an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride, or a combination thereof. The mixed material 21 with the thermoplastic resin fiber containing the mixture as a monomer component is supplied to the recess 153 by air conveyance. Cellulose-based water-absorbing fibers and thermoplastic resin fibers are supplied to the recesses 153 in a mixed state, and a fiber material layer is formed in the recesses 153. The fiber material layer formed in the recess 153 is laminated on the upper surface of the laminated body 223 (the upper surface of the upper core wrap) on the carrier sheet 150 that proceeds in the MD direction, whereby the laminated body 224 is formed.

[Second step]
The laminated body 224 on the carrier sheet 150 travels away from the peripheral surface 151a of the suction drum 151 in the MD direction. The heating unit 103 blows air heated to 135 ° C. at a wind speed of 5 m / sec against the upper surface of the laminate 224 (the upper surface of the fiber material layer). Thereby, the thermoplastic resin fiber contained in the fiber material layer is melted, and the thermoplastic resin fibers and the thermoplastic resin fiber-pulp are bonded (heat fusion). The conditions (temperature, wind speed, heating time) of the heated air sprayed on the laminated body 224 are appropriately controlled according to the production speed and the like.

[Third step]
The breathable mesh conveyor belts 171 and 172 arranged vertically so as to form a pair run in the MD direction while compressing the laminated body 225 that has undergone the heat treatment. The dimension in the vertical direction d (distance between the mesh conveyor belts 171 and 172) in the parallel traveling unit 175 is the gap between the upstream upper roll 176 and the upstream lower roll 177 rotating in the MD direction, and the downstream upper roll 178 The laminated body 225 is set to a required value by adjusting the gap with the downstream lower roll 179, and the laminated body 225 is compressed to a required thickness by the mesh conveyor bare belts 171 and 172. In FIG. 5, a steam jetting part 173 and a steam suction part 174 are arranged on the parallel running part 175 extending horizontally so as to face each other with the mesh conveyor belts 171 and 172 interposed therebetween. For example, nozzles (not shown) having a diameter of 0.1 to 2 mm are stacked at a pitch of 0.5 to 10 mm, preferably 0.5 to 5 mm, and more preferably 0.5 to 3 mm. It is arranged in a crossing direction (CD direction) orthogonal to the MD direction and the vertical direction TD so as to cross 225, and each nozzle has water vapor at a temperature equal to or higher than the boiling point of water generated in the steam boiler 180, For example, high-pressure steam adjusted to a vapor pressure of 0.1 to 2.0 MPa is supplied by the pressure control valve 181 via the pipe 182. From each nozzle, high-pressure steam is sprayed through the mesh conveyor belt 171 to the laminated body 225 which is compressed by the mesh conveyor belts 171 and 172. The amount of high-pressure steam sprayed onto the laminate 225 is adjusted according to the traveling speed of the mesh conveyor belts 171 and 172, and when the mesh conveyor belts 171 and 172 are traveling at 5 to 500 m / min, the mesh conveyor are preferably injected at a range of 1.23kg / m ² ~0.03kg / m ² of the surface area of the laminate 225 faces the belt 171. In the thickness direction of the laminated body 225, the water vapor passes through the mesh conveyor belt 171, the laminated body 225, and the mesh conveyor belt 172 in order, and is recovered by the suction action of the vacuum pressure by the steam suction unit 174. The laminated body 225 injected with the high-pressure steam proceeds in the MD direction, is separated from the mesh conveyor belts 171 and 172, and proceeds to the fourth step. A collar portion and a groove portion are formed on the surface of the laminated body 225 to which the high-pressure steam is injected. By adjusting the number, pitch, etc. of the nozzles of the steam injection unit 173, the number, interval, etc. of the flanges and grooves can be adjusted. Note that the portion where the high-pressure water vapor is injected becomes a groove.

  In the third step, in order to prevent the laminated body 225 from being locally compressed by the mesh conveyor belts 171 and 172, at least one of the mesh conveyor belts 171 and 172 can be easily deformed in the vertical direction TD. Those having a degree of flexibility are used. For the mesh conveyor belts 171 and 172, metal wire mesh belts made of stainless alloy, bronze, etc., plastic mesh belts made of polyester fiber, aramid fiber, etc. can be used. A metal belt formed of a plate may be used instead of the mesh belt. When the laminated body 225 extremely dislikes the mixing of metal powder, it is preferable to use a plastic mesh belt. Further, when a plastic mesh belt is required to have high heat resistance, it is preferable to use a mesh belt made of polyphenylene sulfide resin. A 10-75 mesh plain weave mesh belt using polyphenylene sulfide resin is an example of a particularly preferable mesh belt which has flexibility and can be used for both the mesh conveyor belt 171 and the mesh conveyor belt 172. It is preferable that the steam injection unit 173 and the pipe 182 are provided with appropriate heat retention measures or provided with a drain discharge mechanism. By doing so, it is possible to prevent the drain generated in the steam injection unit 173 and the like from being ejected from the nozzle and excessively containing moisture in the stacked body 225. The water vapor sprayed toward the laminated body 225 includes a dry steam that does not include a liquid component that is moisture, a saturated vapor, and a wet vapor that includes a liquid component. If the water vapor is wet or saturated steam, the pulp can be easily wetted and deformed. Dry steam can vaporize moisture contained in the pulp, and the vaporized moisture can facilitate the deformation of the pulp. Moreover, if the pulp is a thermoplastic synthetic fiber, the thermoplastic synthetic fiber can be easily deformed by the heat of the dry steam. The steam injection unit 173 may be provided with a heating mechanism to change the steam into superheated steam and spray it. It is preferable that the steam suction unit 174 has a pipe that allows the sucked high-pressure steam to go to an exhaust blower (not shown) after passing through the steam separator. In addition, the position of the steam injection part 173 and the steam suction part 174 may be switched, that is, the steam injection part 173 may be on the lower side and the steam suction part 174 may be on the upper side. Further, when it is not necessary to recover the high-pressure steam, the steam suction 174 can be performed without being arranged.

[Fourth step]
The pair of rolls 300 and 301 is an integrated unit that heat-embosses the laminated body 226 that has undergone the high-pressure steam spraying process, and integrates the storage layer (the fiber material layer that has undergone the high-pressure steam spraying process in this embodiment) and the upper layer core wrap. Is formed as a pressing part. The pair of rolls 300 and 301 may form an integrated portion that integrates the lower layer core wrap together with the reservoir layer and the upper layer core wrap as the pressing portion. The roll 300 is an upper roll provided with convex portions (not shown) on the outer peripheral surface, and the roll 301 is a lower roll having a smooth outer peripheral surface. The convex portions of the roll 300 are formed so as to correspond to the shape, arrangement pattern, and the like of the compressed portion, and the reservoir layer and the upper layer core wrap are compressed in the thickness direction of the laminate 226 by these convex portions and heated. Is done. Thereby, the integrated part which unifies a storage layer and an upper layer core wrap is formed as a pressing part. The squeezed part formed in this way is consolidated and has a smaller thickness and a higher density than other parts.

  The rolls 300 and / or 301 are heated and can be heated during compression. In the embossing treatment by the rolls 300 and 301, the heating temperature is usually 80 to 140 ° C., preferably 90 to 120 ° C., and the linear pressure (pressing force per unit width of the pressing part) is usually 10 to 200 N / mm, Preferably it is 40-100 N / mm, and a processing speed is 10-500 m / min normally, Preferably it is 20-300 m / min.

  Production of diapers using the absorbent body 4 thus produced can be carried out according to a conventional method.

Hereinafter, although this invention is demonstrated further in detail based on a manufacture example and a test example, the scope of the present invention is not limited to a manufacture example and a test example.
In the production examples, the following heat-fusible composite fibers and superabsorbent resin particles were used.
As heat-sealable conjugate fiber A (hereinafter referred to as “composite fiber A”), polyethylene terephthalate (PET) as a core component, and high-density polyethylene (HDPE) graft-polymerized with a vinyl polymer containing maleic anhydride as a sheath component A core-sheath type composite fiber was used. The core-sheath ratio of the composite fiber A is 50:50 (mass ratio), the amount of titanium oxide in the core component is 0.7% by weight, the fineness is 2.2 dtex, and the fiber length is 6 mm.

  A core-sheath type composite fiber having polyethylene terephthalate (PET) as a core component and general high-density polyethylene (HDPE) as a sheath component was used as the heat-fusible conjugate fiber B (hereinafter referred to as “composite fiber B”). . The core-sheath ratio of the composite fiber B is 50:50 (mass ratio), the amount of titanium oxide in the core component is 0.7% by weight, the fineness is 2.2 dtex, and the fiber length is 6 mm.

  Polyacrylate cross-linked particles (manufactured by Sumitomo Seika Co., Ltd.) were used as highly water-absorbent resin particles (hereinafter referred to as “SAP particles”). The particle size distribution of the SAP particles is 3.9% for 150 to 250 μm, 5.3% for 250 to 300 μm, 17.1% for 300 to 355 μm, 56.3% for 355 to 500 μm, and 11.3% for 500 to 600 μm. 2%, 600 to 710 μm is 4.9%, 710 to 850 μm is 1.2%, and 850 μm or more is 0.1%.

[Example 1]

(1) Preparation of fiber material A (A1 to A7) Pulp (manufactured by Warehauser, NB416) and composite fiber A were mixed with 9: 1 (A1), 8: 2 (A2), and 6.5: 3.5. (A3), 5: 5 (A4), 3.5: 6.5 (A5), 2: 8 (A6), mixed with a mass ratio of 0:10 (A7), and fiber materials A1 to A7 (basis weight) 200 g / m ² ) was prepared.

(2) Preparation of fiber material B (B1 to B9) Pulp (manufactured by Warehauser, NB416) and composite fiber B were mixed with 9: 1 (B1), 8.5: 1.5 (B2), and 8: 2. (B3), 6.5: 3.5 (B4), 5: 5 (B5), 3.5: 6.5 (B6), 2: 8 (B7), 0:10 (B8), 10: 0 Blending was carried out at a mass ratio of (B9) to prepare fiber materials B1 to B9 (basis weight 200 g / m ² ).

(3) Production of reservoirs A (A1 to A7) and B (B1 to B9) The fiber materials A1 to A7 and B1 to B9 are bonded by a general through air method, and the composite fibers A and B are heated and fused. Reservoir samples A1 to A7 and B1 to B9 were prepared. At this time, the heating temperature was set to 135 ° C., the air volume was set to 5 m / second, and the heating time was set to 20 seconds.

(4) Measurement of maximum tensile strength [maximum tensile strength during drying (N / 25 mm)]
Sample pieces (length 150 mm x width 25 mm, 5 pieces) at standard time (temperature 20 ° C, humidity 60%) are attached to a tensile tester (Shimadzu Corporation, AG-1kNI) at a grip interval of 100 mm, and a tensile speed of 100 mm / min. Then, a load (maximum point load) was applied until the sample piece was cut, and the maximum tensile strength per 25 mm width in the length direction (MD direction) of the sample piece was measured.

[Maximum tensile strength when wet (N / 25mm)]
After immersing a sample piece (length 150 mm x width 25 mm) in ion-exchanged water until it sinks under its own weight, or after submerging the sample piece in water for 1 hour or longer, the length direction of the sample piece is the same as above. The maximum tensile strength per 25 mm width in the (MD direction) was measured.

Regarding the measurement of the maximum tensile strength when dry and wet, the measurement conditions described in ISO 9073-3 or JIS L 1913 6.3 were adopted for the measurement conditions not particularly specified above.
The measurement of the maximum tensile strength during drying and wetness in other examples was also performed in the same manner as described above.

(5) Measurement of the basis weight, thickness and density of the reservoir

[Basis weight]
The measurement of the basic weight (g / m ² ) of the reservoir was performed as follows.
Three sample pieces of 100 mm × 100 mm are cut out from the reservoir, and the mass of each sample piece in a standard state (temperature 23 ± 2 ° C., relative humidity 50 ± 5%) is directly indicated by a balance (Electric Balance HF manufactured by Kensei Kogyo Co., Ltd.) −300), and the mass per unit area (g / m ² ) of the reservoir calculated from the average of the three measured values was taken as the basis weight of the reservoir.
In addition, regarding the measurement of the basis weight of the reservoir, the measurement conditions described in ISO 9073-1 or JIS L 1913 6.2 were adopted for the measurement conditions not particularly specified above.

[Thickness]
The thickness (mm) of the reservoir was measured as follows.
Reservoir in standard condition (temperature 23 ± 2 ° C, relative humidity 50 ± 5%) by thickness gauge (FS-60DS, manufactured by Daiei Scientific Instruments Co., Ltd., measuring surface 44mm (diameter), measuring pressure 3g / cm ² ) 5 parts with different diameters (the diameter of each part is 44 mm) at a constant pressure of 3 g / cm ² , the thickness of each part after 10 seconds of pressurization is measured, and the average value of the five measurements is the thickness of the reservoir It was.

[density]
The density of the reservoir was calculated based on the following formula.
D (g / cm ³ ) = B (g / m ² ) / T (mm) × 10 ⁻³
[In formula, D, B, and T represent the density, basic weight, and thickness of a reservoir layer, respectively. ]
In addition, the measurement of the basic weight, thickness, and density of the sample in another Example was implemented similarly to the above.

(6) Results and discussion Table 1 shows the measurement results.

The consideration based on Table 1 is as follows.
In the reservoir layer A, when the mixing ratio (mass ratio) of the composite fiber A to the pulp is less than 1/9, the maximum tensile strength when wet is expected to be less than 2 N / 25 mm, and the strength when wet is insufficient. There is a risk. Therefore, in the reservoir A, it is considered that the mixing ratio (mass ratio) of the composite fiber A to the pulp is preferably 1/9 or more from the viewpoint of maintaining strength.

  In the reservoir B, when the mixing ratio (mass ratio) of the composite fiber B to the pulp is 1.5 / 8.5 or less, the maximum tensile strength when wet is less than 2 N / 25 mm, and the strength when wet is insufficient. There is a risk of becoming. Therefore, in the reservoir B, it is considered that the mixing ratio (mass ratio) of the composite fiber B to the pulp is preferably higher than 1.5 / 8.5 from the viewpoint of maintaining strength.

  When the reservoirs having the same mixing ratio (mass ratio) between the pulp and the composite fibers A and B (for example, the reservoir A1 and the reservoir B1) are compared, the maximum tensile strength (when dry and wet) is Also in the mixing ratio (mass ratio), the reservoir A is larger than the reservoir B. Moreover, when the mixing ratio (mass ratio) of pulp and composite fibers A and B is in the range of 9: 1 to 3.5: 6.5 (reservoir layers A1 to A5, B1 to B6), the maximum during drying The difference between the tensile strength and the maximum tensile strength when wet (the maximum tensile strength when dry-the maximum tensile strength when wet) is greater in the reservoir A than in the reservoir B.

  In the reservoir A, a hydrogen bond is generated between the acyl group of maleic anhydride and the oxygen atom of the ether bond in the reservoir A and the OH group of cellulose. Such a hydrogen bond is considered to be caused by no occurrence.

  This is also supported by the maximum tensile strength of the web sample. That is, when the maximum tensile strength of the sample in the web state was measured, all samples were less than 0.4 N / 25 mm (see Table 1), and the difference in strength was not caused by the difference in the degree of entanglement. This suggests that it is caused by the presence or absence of hydrogen bond formation. The web sample is an unprocessed sample after laminating the fiber material on the base material, entanglement treatment such as needle punch, heat treatment by hot air, embossing, energy wave, adhesive, etc. No processing such as processing by is performed.

  In addition, as shown in Table 2 below, because the composite fiber A has a higher heat of fusion than the composite fiber B, the composite fiber A has a higher crystallinity than the composite fiber B, and the difference in strength is as follows. , B is considered to be caused by a difference in crystallinity (bonding strength of the fiber itself).

  In JP-A-2004-270041, a modified polyolefin obtained by graft polymerization of maleic anhydride is bonded to a cellulose fiber because a carboxylic anhydride group of maleic anhydride is cleaved and covalently bonded to a hydroxyl group on the surface of the cellulose fiber. However, in this result, an increase in strength due to the formation of a covalent bond was not observed.

[Example 2]
(1) Production of reservoirs C (C1 to C7) and D (D1 to D9) Fiber materials A1 to A7 (see Example 1) are placed on a carrier sheet (UCCKN, tissue basis weight: 14 g / m ² ). The composite fiber A is heated and fused (heating temperature: 135 ° C., air volume: 5 m / second, heating time: 20 seconds), and then a steam jet (SJ) belt press machine. at adjusted to a density of about ^{0.08g / cm 3 (0.0793~0.0817g / cm} 3), was produced reservoir C1~C7 (120mm × 120mm, the three).
Reservoir layers D1 to D9 (120 mm × 120 mm, 3 sheets each) were similarly manufactured using fiber materials B1 to B9 (see Example 1).

The structure of the used SJ belt press is shown in FIG.
As shown in FIG. 6A, the SJ belt press machine 9 includes mesh conveyor belts 91a and 91b, a steam nozzle 92, and a suction box 93, and the steam nozzle 92 and the suction box 93 facing each other. The fiber material layer sandwiched between the pair of mesh conveyor belts 91a and 91b is conveyed therebetween, and high-pressure steam is jetted from the steam nozzle 92 toward the fiber material layer to compress the fiber material layer. The water vapor that has passed through the fiber material layer is sucked by the suction box 93 and exhausted. The thickness of the fiber material layer can be adjusted by adjusting the distance between the pair of mesh conveyor belts 91a and 91b.

  The mesh conveyor belts 91a and 91b are polyphenylene sulfide plain weave mesh conveyors (manufactured by Nippon Filcon Co., Ltd.). The vertical and horizontal wire diameters are 0.37 mm, the vertical lines are 34 / inch, and the horizontal lines are 32 / inch. The distance between the mesh conveyor belts 91a and 91b is adjusted to 1 mm or 0.2 mm, and the line speed is 200 m / sec.

As shown in FIG. 6B, the steam nozzle 92 is formed with openings having a diameter of 0.5 mm with an opening pitch of 2 mm and 5 mm, and the steam pressure of water vapor ejected therefrom is 0.7 MPa. Yes, the steam throughput is 1.27 kg / m ² per unit area.

(2) Measurement of absorbency (penetration time, liquid brushing time) A top sheet (product name: Sophie Hadaoi Top Sheet) is placed on the reservoir, and a perforated acrylic plate (40 mm x 10 mm in the center) is placed on it. , 200 mm (length) × 100 mm (width)). Using autoburet (Shibata Chemical Instruments Co., Ltd., Multidojimat E725-1 type), artificial menstrual blood (80 g of glycerin, 1 liter of ion-exchanged water, sodium carboxymethylcellulose) toward the hole in the acrylic plate 8 g, sodium chloride 10 g, sodium hydrogen carbonate 4 g, red No. 102 8 g, red No. 2 2 g and yellow No. 5 2 g were used, and 3 ml was injected at 90 ml / min. The time from the start of injection until the artificial menstrual blood staying in the hole in the acrylic plate disappeared was the permeation time (seconds), and the time from the start of injection until the artificial menstrual blood disappeared from the surface sheet was taken as the brush time (seconds) .

(3) Measurement of the maximum tensile strength at the time of drying and wet The maximum tensile strength at the time of drying and wet of the reservoir layer was measured in the same manner as in Example 1.

(4) Results and discussion Table 3 shows the measurement results.

  As shown in Table 3, when the mixing ratio (mass ratio) of pulp and composite fiber A is in the range of 9: 1 to 5: 5 (reservoir layers C1 to C4), the absorbency of the reservoir layer is sufficient. However, when the mixing ratio (mass ratio) of the pulp and the composite fiber A is in the range of 3.5: 6.5 to 0:10 (reservoir layers C5 to C7), the absorbability of the reservoir layer is remarkably high. Declined.

  As shown in Table 3, when the mixing ratio (mass ratio) of the composite fiber A to the pulp is less than 1/9 in the reservoir layer C, the maximum tensile strength when wet is expected to be less than 2 N / 25 mm. There is a risk that the strength at the time will be insufficient. Therefore, in the reservoir layer C, it is considered that the mixing ratio (mass ratio) of the composite fiber A to the pulp is preferably 1/9 or more from the viewpoint of maintaining strength.

  As shown in Table 3, in the reservoir layer D, when the mixing ratio (mass ratio) of the composite fiber B to the pulp is 1.5 / 8.5 or less, the maximum tensile strength when wet is less than 2 N / 25 mm, There is a risk that the strength when wet will be insufficient. Therefore, in the reservoir D, it is considered that the mixing ratio (mass ratio) of the composite fiber B to the pulp is preferably higher than 1.5 / 8.5 from the viewpoint of maintaining strength.

From the results shown in Table 3, when the density of the reservoir is about 0.08 g / cm ³ (0.0793-0.0817 g / cm ³ ), the mixing ratio (mass ratio) of the pulp and the composite fiber A is 9 In the range of 1 to 5: 5, it was revealed that the reservoir layer has sufficient strength and absorbency. This is because the composite fiber A can secure the strength of the reservoir in a smaller amount than the composite fiber B (thus, without inhibiting the absorbability).

Example 3
In Example 2, the fixed system a density of about ^{0.08g / cm 3 (0.0793~0.0817g / cm} 3), the mixing ratio of the intensity and from the standpoint of the absorbent, pulp and composite fibers A (mass Ratio) was examined.
In this example, the optimum range of density was examined from the viewpoint of absorbability.

In the same manner as in Example 2, using a pulp (basis weight 200 g / m ² ) obtained by blending pulp (Warehauser, NB416) and composite fiber A at a mixing ratio (mass ratio) shown in Table 4, Reservoirs E1 to E9 of various densities (0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.12, 0.13, 0.14 g / cm ³ ) Manufactured and measured for absorbency (liquid brush time).
Table 4 shows the measurement results.

From the measurement results shown in Table 4, the following became clear.
When the mixing ratio (mass ratio) of pulp and composite fiber A is in the range of 9: 1 to 5: 5, sufficient liquid brush performance (specifically, the liquid brush time after dropping 3 cc of artificial menstrual blood is 90. (Within seconds) is 0.06 to 0.14 g / cm ³ .

When the density is less than 0.06 g / cm ³ , the liquid brush time exceeds 90 seconds at any mixing ratio. If the density is less than 0.06 g / cm ³ , it is considered that the interfiber distance is large and the capillary force does not act.

When the density exceeds 0.12 g / cm ³ , the liquid brushing time is within 60 seconds when the mixing ratio (mass ratio) of the pulp and the composite fiber A is in the range of 9: 1 to 6.5: 3.5. However, in other ranges, it exceeds 60 seconds. When the density exceeds 0.12 g / cm ³ , the capillary action works, but the liquid movement gap becomes small and the liquid movement resistance increases, so the liquid brushing performance is considered to deteriorate.

From the results of Examples 1 to 3, the optimum range of the mixing ratio (mass ratio) of pulp and composite fiber A is 9: 1 to 5: 5, and the optimum density is 0.06 to 0.14 g / cm ³ . It became clear that there was.

Example 4
(1) Production of fiber material F (F1 to F4) Pulp (manufactured by Warehauser, NB416) and composite fiber A are mixed with 9: 1 (F1), 8.8: 2 (F2), and 6.5: 3. .5 (F3) and 5: 5 (F4) were blended to produce fiber materials F1 to F4 (basis weight 200 g / m ² ).

(2) Manufacture of fiber material G (G1 to G5) Pulp (manufactured by Werehauser, NB416) and composite fiber B were mixed with 9: 1 (G1), 8: 2 (G2), and 6.5: 3.5. (G3) Cotton blended at a mass ratio of 5: 5 (G4) and 10: 0 (G5) to produce fiber materials G1 to G5 (basis weight 200 g / m ² ).

(3) Production of storage layers F (F1 to F4) and G (G1 to G5) The fiber materials F1 to F4 and G1 to G5 are bonded by a general through-air method, and the composite fibers A and B are heated and fused. The reservoirs F1 to F4 and G1 to G5 were manufactured. At this time, the heating temperature was set to 135 ° C., the air volume was set to 5 m / second, and the heating time was set to 20 seconds.

(4) Manufacture of integrated samples F (F1 to F4) and G (G1 to G5) On the lower surface of the reservoirs F (F1 to F4) and G (G1 to G5), a tissue made by Unicharm Kokumi Non-Woven Co., Ltd. (Composition: NBKP (beating) 67.9%, NBKP (non-beating) 29.1%, paper strength enhancer (polyacrylamide) 2.14%, paper strength enhancer (polyamide epichlorohydrin) 0 .86%, Basis weight: 20 g / m ² , MD direction strength (maximum point strength): 16.8 N / 25 mm, CD direction strength (maximum point strength): 2.9 N / 25 mm, thickness: 0.1 mm) , And a heat embossing treatment is performed from the side of the reservoir, and the reservoirs F (F1 to F4), G (G1 to G5) and the tissue are integrated at the embossed part F (F1 to F4), G (G1-G5) was manufactured.

  In the heat embossing process, a plate on which a large number of convex portions are formed as an embossing plate on the storage layer side (upper side) (tip diameter of each convex portion: 3 mm, pitch between convex portions: 10 mm long × 10 mm wide, each convex portion The height was 5 mm, the heating temperature was 120 ° C., a flat plate (heating temperature: 120 ° C.) was used as the tissue-side (lower) embossing plate, the pressure was 3 Mpa, and the embossing time was 3 seconds. .

(5) Measurement of interfacial peel strength The interfacial peel strength when the integrated samples F (F1 to F4) and G (G1 to G5) were dried and wet was measured.
[Interfacial peel strength during drying (N / 25mm)]
Standard sample (temperature 20 ° C, humidity 60%) sample piece (length 40mm x width 25mm, including 8 embossed parts) is gripped by a tensile tester (Shimadzu Corporation, AG-1kNI) at an interval of 20mm. A reservoir was attached to the tissue, and a tissue was attached to the lower grip. A load was applied at a tensile speed of 100 mm / min until the sample piece completely peeled, and the interfacial peel strength per 25 mm width in the length direction (MD direction) of the sample piece was measured.

[Interfacial peel strength when wet (N / 25 mm)]
After immersing a sample piece (length 40 mm x width 25 mm) in ion-exchanged water until it sinks under its own weight, or after submerging the sample piece in water for 1 hour or longer, the length direction of the sample piece is the same as above. The interfacial peel strength per 25 mm width in the (MD direction) was measured.

  Regarding the measurement of the interfacial peel strength when dry and wet, the measurement conditions described in ISO 9073-3 or JIS L 1913 6.3 were adopted as the measurement conditions not particularly specified above.

(2) Results and discussion Table 5 shows the measurement results.

The consideration based on Table 5 is as follows.
When the interfacial peel strength between the reservoir layer and the covering layer (tissue in this embodiment) covering the absorbent core is less than 0.98 N / 25 mm, the reservoir layer and the absorbent core are removed during use of the absorbent article. Interfacial peeling with the coating layer to coat may occur, and the liquid transferability from the reservoir layer to the absorbent core may deteriorate. Therefore, based on the fact that both the dry and wet interfacial peel strengths are 0.98 N / 25 mm or more, the integrated samples F1 to F4 satisfy this standard. Therefore, the mass mixing ratio of the composite fiber A to the pulp in the reservoir is 1/9 or more, which is advantageous in terms of increasing the interfacial peel strength during drying and wetting, and thereby 1.75 N / 25 mm or more. The interfacial peel strength when dried and the interfacial peel strength when wet of 1.05 N / 25 mm or more can be realized. Further, by setting the mass mixing ratio of the composite fiber A to the pulp in the reservoir layer to 1/9 to 5/5, the interfacial peel strength during drying of 1.75 to 4.23 N / 25 mm, and 1.05 to 2. An interfacial peel strength of 63 N / 25 mm can be achieved.

  Comparing integrated samples (ie, F1 and G1, F2 and G2, F3 and G3, and F4 and G4) having the same mass mixing ratio of the composite fibers A and B to the pulp in the reservoir layer, when dry and wet The interfacial peel strength is greater in the integrated sample F than in the integrated sample G at any mass mixing ratio. Therefore, when the mass mixing ratio of the composite fibers A and B to the pulp in the reservoir layer is the same, when using the composite fiber A, the interfacial peel strength at the time of drying and wetting is higher than when using the composite fiber B. Can be increased. In addition, when it is desired to achieve a constant dry and wet interfacial peel strength, the mass mixing ratio of the composite fiber to the pulp in the reservoir layer is smaller when the composite fiber A is used than when the composite fiber B is used. (That is, the mass mixing ratio of the pulp in the reservoir increases correspondingly, and the absorption performance of the reservoir can be improved).

1 disposable diaper (an example of an absorbent article)
2 Top sheet (an example of a liquid-permeable layer)
3 Back sheet (an example of a liquid-impermeable layer)
4 Absorbent body 41 Reservoir layer 42 Absorbent core 43a, 43b Core wrap (an example of a coating layer)
44 Integrated part

Claims (10)

A storage layer for temporarily storing liquid, an absorbent core that absorbs the liquid stored in the storage layer, a coating layer that covers a surface of the absorbent core on the storage layer side, the storage layer, and the coating an absorbent body having a integral part of one body of the layer,
The reservoir layer contains a cellulosic water-absorbing fiber and a thermoplastic resin fiber containing an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride or a mixture thereof as a monomer component,
The absorbent core contains a superabsorbent polymer material;
The coating layer contains cellulosic water-absorbing fibers ,
In the integrated portion, the absorbent body in which the thermoplastic resin fibers contained in the storage layer are thermally fused with the cellulose water-absorbing fibers contained in the coating layer .   The absorbent body according to claim 1, wherein fibers contained in the storage layer are bonded to each other.   The interfacial peel strength during drying of the reservoir layer and the coating layer is 1.75 to 4.23 N / 25 mm, and the interfacial peel strength when wet of the reservoir layer and the coating layer is 1.05 to 2.63 N / 25 mm. The absorber according to claim 1 or 2.   The absorber according to any one of claims 1 to 3, wherein a mass ratio of the thermoplastic resin fibers to the cellulosic water-absorbing fibers in the reservoir layer is 1/9 to 5/5. The absorber according to claim 4, wherein the density of the reservoir layer is 0.06 to 0.14 g / cm ³ . The absorbent body according to claim 5, wherein a basis weight of the reservoir is 40 to 900 g / m ² .   The thermoplastic resin fiber is a modified polyolefin graft-polymerized with a vinyl monomer containing an unsaturated carboxylic acid, an unsaturated carboxylic anhydride or a mixture thereof, or a mixed polymer of the modified polyolefin and another resin as a sheath component, The absorbent body according to any one of claims 1 to 6, which is a core-sheath type composite fiber having a resin whose melting point is higher than that of the modified polyolefin as a core component.   The unsaturated carboxylic acid, the unsaturated carboxylic acid anhydride or a mixture thereof is maleic acid or a derivative thereof, maleic anhydride or a derivative thereof, or a mixture thereof. Absorber.   The absorber according to any one of claims 1 to 8, wherein a difference between a maximum tensile strength at the time of drying and a maximum tensile strength at the time of moisture in the reservoir is 1 to 5 N / 25 mm. An absorbent article comprising a liquid permeable layer, a liquid impermeable layer, and the absorber according to any one of claims 1 to 9,
The absorbent article, wherein the absorber is provided between the liquid permeable layer and the liquid impermeable layer so that the storage layer is located between the liquid permeable layer and the absorbent core. .

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