![]() Unitary fluid acquisition, storage, and wicking material
专利摘要:
A fluid collection layer; A fluid distribution layer; And a fluid storage layer between the collection layer and the distribution layer. The collecting, dispensing and storage layers are each adapted to transfer fluids to each other. 公开号:KR20020040674A 申请号:KR1020017015760 申请日:2000-06-08 公开日:2002-05-30 发明作者:사무엘찰스 베어;수-강로렌스 리;존피. 어스파머;제임스리차드 그로스 申请人:비케이아이 홀딩 코포레이션; IPC主号:
专利说明:
UNIQUE FLUID ACQUISITION, STORAGE, AND WICKING MATERIAL} [2] Absorbent products, such as disposable diapers, adult incontinence pads, sanitary napkins and the like, are generally provided with an absorbent core or storage layer for receiving or retaining body secretion. The absorbent core is generally sandwiched between a liquid permeable surface sheet that allows the fluid to reach the core and a liquid impermeable back sheet that contains the fluid and prevents the fluid from exiting the absorbent product. Absorbent cores (eg, for diapers and adult incontinence pads) generally comprise fibrous batts or webs composed of defiberized, loose and fluffed hydrophilic cellulose fibers. The core may comprise superabsorbent polymer (SAP) particles, granules, flakes or fibers. In addition, the absorbent article may include a distribution layer that facilitates rapid delivery of liquid from the collection layer to the storage layer of the core. Conventional absorbent products are complicated by production lines using individually formed layers for collection, distribution and storage. Thus, there is a need for an absorbent product in which the collection, distribution and storage functions are all within a single integrated structure. [3] There is an increasing market demand for thinner and more comfortable absorbent products. Such products can be obtained by reducing the amount of fibrous material used in the core and increasing the amount of SAP particles, or by reducing the thickness and increasing the density by calendering or compressing the core to make the diaper core thinner. However, if the core is denser, the effective pore size becomes smaller, so that the high density core does not absorb liquid as quickly as the low density core. Thus, in order to maintain a moderate liquid absorption rate, it is necessary to provide a low density layer having a larger pore size than the high density absorption core to increase the collection rate for the liquid discharged on the absorbent article. In general, the absorbent structure has a problem in that the pore size is inappropriate to absorb a large amount of rapidly discharged fluid. There is a great need for an absorbent structure having a collection layer with sufficient pore size to accommodate rapid flow of fluid. [4] In a conventional multilayer absorbent structure having a collection layer, a distribution layer and a storage layer, the collection layer collects liquid insults and quickly moves them away from the wearer's skin through capillary action (Z-direction). . The fluid then reaches the distribution layer. The distribution layer is generally a high density material that allows liquid to move away from the wearer's skin (Z-direction) and to move from side to side across the structure (X-Y direction). Finally, the liquid moves to the storage layer. The storage layer generally comprises high density cellulose fibers and SAP particles. The liquid is absorbed by the storage layer and in particular the SAP particles contained therein. [5] Although the conventional multilayer structure described above can be effective, one drawback of this arrangement is that the distribution layer is on the side of the storage layer facing the wearer's skin, and due to the relatively low fluid retention of the distribution layer, There is a possibility of standing on the wearer's skin before being absorbed into the storage layer. As the wearer moves, pressure is generated to release the fluid, which causes the wearer to get wet again. Therefore, it would be desirable to provide a structure that immediately collects liquid and moves it away in the Z-direction away from the wearer's skin and absorbs it into the storage layer to minimize or eliminate the problem of liquid contacting the wearer's skin again. [1] The present invention relates to an improved fibrous absorbent structure having individual layers as areas for collection, storage and distribution of fluids. This structure is useful for providing improved disposable absorbent products such as diapers, adult incontinence pads, and sanitary napkins. [28] 1 is a schematic cross-sectional view of a conventional multilayer absorbent structure, [29] 2 is a schematic cross-sectional view of one embodiment of a single multilayer absorbent structure of the present invention; [30] 3 is a schematic cross-sectional view of a fluid absorption path through a single multilayer absorbent structure of the present invention. [6] The present invention provides a fluid collection layer; A fluid distribution layer; And a fluid storage layer between the collection layer and the distribution layer. The collection, distribution, and storage layers each allow fluids to be transferred to each other. [7] All references cited in this application are fully incorporated by reference. In case of inconsistency, the detailed description of the invention is intended to cover the definition thereof. [8] The present invention includes a collection layer that collects liquid insult and moves it away from the wearer's skin (in the Z-direction) through capillary action; A storage layer containing high density matrix fibers and SAP particles; And single, multi-zone or multilayer absorbent structures having a distribution layer that absorbs and retains some of the excess liquid through the storage layer. As used herein, the term "layer" refers to a layered region that constitutes a single structure. A layer of a unitary structure is not a layered structure or assembly of preformed layers that form a multilayer structure. The unitary structure is instead constructed by combining the layers in a continuous manner. Airlaid technology is the preferred method for combining the unitary structure layers of the present invention. [9] In one embodiment, the distribution layer comprises a fibrous matrix material and moves the liquid from side to side (in the XY direction) across the structure and back to the storage layer such that the liquid is absorbed and retained by the SAP particles in the storage layer. To be. By this arrangement, the liquid in contact with the structure can be moved away from the user's skin and absorbed throughout the structure into the storage layer where there is less tendency to retain or clog moisture at the interface of the wearer's skin and the structure. The invention also includes an absorbent structure having a collecting layer with increased pore size. [10] In one preferred embodiment, the absorbent structure of the present invention comprises three or more layers, all of which are intended to allow fluids to be transferred to each other. These layers include a fluid collection (top) layer, a fluid storage (middle) layer and a fluid distribution (bottom) layer. [11] The fluid collection (top) layer may comprise polyester (eg, PET) and / or synthetic homopolymer fibers; 0-10% SAP; And thermal or latex binder resins; Typically a basis weight of 20-120 gsm (grams per square meter). The fluid storage (middle) layer may comprise fluff cellulose and / or chemically modified cellulose fibers; 10-75% SAP; And a thermal binder resin; Generally the base weight is 60-400gsm. The fluid distribution (bottom) layer may comprise fluff cellulose and / or chemically modified cellulose fibers; 0-10% SAP; And thermal and / or latex binder resins; Typically the basis weight is 20-200 gsm. [12] A second preferred embodiment of the present invention comprises four layers of a synthetic fiber collection layer (top), a cellulose fiber collection layer (middle top), a storage layer (middle bottom), and a distribution layer (bottom). [13] The total basis weight range of these composition structures is 100-720 gsm, with an SAP content of 10-75%. Preferred basis weight ranges and SAP content depend on the intended application. For applications in feminine hygiene and low dose adult incontinence, the basis weight and SAP content would be better in the lower end of the range. For application in baby diapers and incontinence articles of high dose adults, the basis weight and the SAP would preferably be in the upper limits of this particular range. [14] The collecting layer is designed to minimize fluid retention. In a preferred embodiment, the matrix fibers of the collection layer are synthetic fibers of at least 2 denier in size and capable of latex bonding. Examples of suitable synthetic fibers include polyesters, polyamides and polyolefins such as polyethylene and polypropylene. In another preferred embodiment, the collection layer comprises matrix fibers comprising 3-40 denier crimp PET fibers with a cut length of 3-12 mm. [15] The storage layer is characterized by a relatively high concentration of superabsorbent polymer (SAP). Forms of superabsorbent polymers usable in the present invention include, for example: certain forms of SAP such as irregular granules, spherical particles, staple fibers and other elongated particles. US Patent No. 5,147,343; 5,378,528; 5,795,439; 5,807,916; And 5,849,211 disclose various superabsorbent polymers and methods of making superabsorbent polymers. One example of a superabsorbent polymer forming system is an acrylic copolymer in which a metal salt of acrylic acid and other monomers such as acrylamide or 2-acrylamido-2-methylpropanesulfonic acid are crosslinked. Many conventional granular superabsorbent polymers are based on poly (acrylic acid) which is crosslinked when polymerized with any of the many multifunctional co-monomer crosslinkers well known in the art. Examples of multifunctional crosslinkers are described in US Pat. No. 2,929,154; 3,224,986; 3,332,909; 4,076,673. For example, crosslinked and carboxylated polyelectrolytes can be used to form superabsorbent polymers. Other water soluble polyelectrolyte polymers are known to be useful in the preparation of superabsorbers via crosslinking, such polymers include carboxymethyl starch, carboxymethyl cellulose, chitosates, gelatin salts, and the like. However, they are generally not used on a commercial scale to improve the absorbency of disposable absorbent articles because of their high cost. Superabsorbent polymer granules useful in the practice of this invention are commercially available from many manufacturers, such as Dow Chemical (Midland, Michigan), Stockhausen, Greensboro, North Carolina, and Chemdal (Arlignton Heights, Illinois). have. In a preferred embodiment, the SAP is a surface crosslinked acrylic acid based powder such as Stockhausen 9350 or SX70. [16] Cells modified to increase the curl and stiffness of each fluff cellulose fiber (e.g. Buckeye HPF modified fluff cellulose) are stored instead of or in addition to the standard fluff cellulose fiber. By using the layer, it is possible to improve the fluid collection and retention of the present invention. [17] The distribution layer distributes the fluid in the x-y direction, allowing the superabsorbent particles in the storage layer remote from the point of fluid insulator to absorb the fluid. This distribution layer also serves to attract fluid not immediately absorbed by the SAP of the storage layer in the z-direction away from the wearer's skin. [18] The matrix fibers of the distribution layer may comprise fluff pulp, modified fluff cellulose or combinations thereof. In a preferred embodiment, the cellulose fibers of the distribution layer are modified to reduce the stiffness of the fibers, making the layers more compact. [19] In a preferred embodiment of the present invention, the fluid distribution layer mainly consists of cellulose fibers whose average pore size is smaller than the fluid collection layer and the pore size is below the pore size of the storage layer. In general, a small average pore size is high density. It is preferred that the density of the distribution layer is greater than the density of the collection and storage layers. If the density of the distribution layer is greater than the density of the collection and storage layers, high fluid collection rates and low stain size factors of the low density absorbent structure and high fluid retention properties of the high density structure can be obtained. [20] In a preferred embodiment, the claimed absorbent structural layers are formed of an airlayed web. The absorbing layers are airlayed on top of a lightweight (e.g. 10-20 gsm) cellulose tissue or similar carrier layer that serves to contain SAP powder during the web forming process, thereby preventing the fiber collection wire from plugging with the SAP particles. do. [21] Airlayed webs are generally made by providing individualized fibers by breaking down or fiberizing cellulose pulp sheets or sheets with a hammer mill. The individualized fibers are then air conveyed to the forming head on the airlayed web former. Some examples of airlaid web formers are disclosed in detail in US Pat. No. 5,527,171 to Soerensen. The forming head may comprise a rotating or stirring drum which serves to maintain fiber separation until the fibers are pulled by vacuum on the foraminous condensing drum or the hole forming conveyor (or forming wire). Other fibers, such as synthetic thermoset fibers, may be introduced into the forming head through a fiber dosing system that includes a fiber opener, a dosing unit, and an air conveyor. If two confined layers are desired, such as a fluff pulp distribution layer and a synthetic fiber collection layer, two separate forming heads may be used for each fiber type. After the fibers are airlayed, the resulting structure is densified and the fibers are bonded together. [22] Generally, calendars are used to densify the resulting structure. It is also possible for all layers to be compressed before airlaying. For example, the first batt of airlayed fibers may be compressed to form a distribution layer having a density of about 0.08 to about 0.20 gr / cc before the next fiber batt is airlayed. [23] The thermosetting binder with the web fibers may be softened to bond the collection, distribution and / or storage layer fibers together. Thermosetting binders include all thermosetting polymers that can melt at temperatures that do not excessively damage cellulose fibers. The melting point of the thermosetting binder material is preferably less than about 175 ° C. Examples of suitable thermosetting materials include thermosetting microfibers, thermosetting powders, binding fibers in the form of staples and bicomponent staple fibers. In particular, thermosetting binding materials are for example polyethylene, polypropylene, polyvinylchloride, polyvinylidene chloride. Other synthetic fiber materials usable for thermally bonded webs are described above. Thermosetting binders may be intermixed with cellulose fibers in an airlayed web former or added to a suitable layer after airlaying. [24] By applying a latex spray, the collection and distribution layers can be selectively or additionally bonded together. Examples of elastomeric polymers available in latex form include butadiene-styrene, butadiene-acrylonitrile and chloroprene (neoprene). Other examples of synthetic polymers usable in latex include polymers or copolymers of alkylacrylates, vinyl acetates such as ethylene vinyl acetate and acrylics such as styrene-butadiene acrylics. For the elimination of solvent recycling steps and industrial hygiene, synthetic latexes can be applied as aqueous emulsions rather than organic solvent emulsions. Latexes useful in the present invention can be prepared by emulsion polymerizing certain olefin (ethylenically unsaturated) monomers. Such emulsion polymerizations may employ alkyl sulfates, alkylarylalkoxy sulfates, alkylarylsulfonates and alkyl- and alkylaryl-polyglycol ethers using any of a variety of anionic, nonionic, cationic, amphoteric and / or amphoteric emulsifiers. Alkali metal and / or ammonium salts of sulfates; Block copolymers of oxyethylated fatty alcohols or oxyethylated alkylphenols and ethylene oxide and propylene oxide; Cationic adducts of primary, secondary or tertiary fatty amines or fatty amine oxyethylates with organic or inorganic acids, and quaternary alkylammonium surfactants; And the obtained latex comprising alkylamidopropylbetaine. The olefin monomers may be monomeric monomers or mixtures with other olefin monomers, ie to form dispersed or emulsified copolymer particles in the water phase. Examples of olefin monomers usable for forming latex polymers include propyl acrylate, n-butyl acrylate, isobutyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, ethyl acrylate and its C 2 -C 4 alkyl and hydroxy alkyl acrylates such as those selected from the mixture group. Other examples include propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, ethyl methacrylate, methyl methacrylate, C 1 -C 4 alkyl or hydroxy alkyl methacrylates selected from the group of vinyl acetate and mixtures thereof. Mixtures of such C 2 -C 4 alkyl and hydroxy alkyl acrylates and C 1 -C 4 alkyl or hydroxy alkyl methacrylates are also suitable. Methods of applying latex include coatings, dipping, brushes, sprays and foaming. In a preferred embodiment, the latex is applied by spray. Latex resins are applicable before and after compression of the fibrous web. [25] The bicomponent staple fibers are high melting point core polymers (typically polyethylene tere) surrounded by low melting point sheath polymers (typically polyethylene (e.g., Hoechst-Trevira Type-255 (Charlotte, NC)), modified polyethylene or copolyesters). Phthalate (PET) or polypropylene). [26] The bonded web can be calendered twice or embossed to have a design or pattern to increase its strength. If thermoset fibers are present, they can be hot calendered to impart pattern bonding to the web. Water may be added to the web if necessary to maintain a specific or desired moisture content, to minimize dusting, or to reduce the build up of static electricity. The processed web is then wound up for later use. [27] The following examples are intended to illustrate the invention and are not intended to limit the scope of the invention. [31] Examples of some of the preferred embodiments of the present invention are listed in Tables 1 and 2. The raw materials of the embodiments described in Tables 1, 2 and 3 are as follows unless otherwise stated: [32] Fluff Cellulose: Buckeye Foley Fluff, Buckeye Technologies Inc., Memphis, TN [33] Binding fiber: Hoechst-Trevira, Charlotte, NC Hoechst-Trevira T-255 [34] Latex binder: Air Products, Allentown PA (Air Products, AirFlex 192) [35] PET fiber: Type D2645 6 denier X 6mm crimp fiber made by fehst-trevirass (Germany) [36] Tissue: 18 gsm (grams per square meter) wet laid [37] Example 1 [38] Single Compression Embodiment-Sample MJ998-MF-17Fluff cellulose (gsm)Bonding fiber (gsm)SAP powder (gsm)Latex Binder Resin (gsm)PET fiber (gsm) Collection layer0.00.00.06.034.0 Storage layer555400.00.0 Distribution layer5730.00.00.0 [39] MJ998-MF17 material was formed on an M & J-type air forming line. First, a cellulose distribution layer was formed on the tissue. A storage layer was then formed over the distribution layer, and then a collection layer was formed on top of the storage layer. The resulting three layers of material were thermally bonded and then compacted by calendering to obtain a total density of 0.142 gr / cc. [40] Example 2 [41] In another embodiment, the distribution layer is first compressed, then the other layers are airlayed and all the layers are compressed together. [42] Double Compression Embodiment-Sample MJ998-MF-18bFluff cellulose (gsm)Bonding fiber (gsm)SAP powder (gsm)Latex Binder Resin (gsm)PET fiber (gsm) Collection layer0.00.00.06.034.0 Storage layer555400.00.0 Distribution layer5730.00.00.0 [43] MJ998-MF-18b material was formed on an M & F-type air formation line. A cellulose distribution layer was formed on a tissue and compressed by calendering to obtain a density of 0.15 gr / cc. After the storage layer was formed on the distribution layer, the collection layer was formed on top of the storage layer. The resulting three layers of material were compressed and then thermally bonded to give a density of total composition material of 0.081 gr / cc. [44] Example 3 [45] The cellulose fibers of the distribution layer are preferably thermally bonded together. Table 3 shows examples of compositions in which the thermally bonded fluff cellulose distribution layer is present at the top of the storage layer and at the bottom of the collection layer. [46] Absorbent Structure with Distribution Layer on Storage Layer-Sample MJ998-MF-9 (Control)Fluff cellulose (gsm)Bonding fiber (gsm)SAP powder (gsm)Latex Binder Resin (gsm)PET fiber (gsm) Collection layer0.00.00.06.034.0 Storage layer5730.00.00.0 Distribution layer555400.00.0 [47] MJ998-MF-9 material was also formed on the M & J-type pilot line. This material represents the structure previously described in that the fluid storage layer is first formed. After the distribution layer was formed on top of the storage layer, the collection layer was formed on top of the distribution layer. The fluff cellulose of the distribution layer was Buckeye HPF fiber. The three layers of structures were thermally bonded and compressed to yield a total density of 0.094 gr / cc. [48] Fluid Collection and Fluid Retention Test [49] The fluid collection test was carried out with the composition material. Each sample (size 10 cm x 25 cm) was wrapped in a suitable coating and placed on a lower fluid absorption test ("FIT") board with the wire or carrier facing downwards. The center of the sample is indicated. [50] The collection rate of the test sample was evaluated by insisting 0.9 ml salt solution three times in succession 10 ml. First insult (10 ml of 0.9% saline solution) was poured into a clean addition tube on the FIT board as soon as possible. The time from the moment of addition until the salt water reached the sample was measured. The stopwatch was stopped as soon as all the brine passed the bottom edge of the tube. The time recorded was the time required for upper collection. At 1 minute intervals, the above procedure was repeated with second and third 10 ml insults. [51] The collection rate from each fluid insert was calculated according to the following formula: [52] Collection rate (ml / s) = [53] After each fluid insulation, a fluid retention test of the composition material was performed by measuring the amount of 0.9% salt solution that could be absorbed through the top sheet of the structure by a large amount of filter paper under 0.1 psi pressure. Samples were prepared for three separate measurements (each measuring 8½ "x 11"). Each sample was placed in a plastic backing with the tissue facing down and the center was marked. 10 ml of 0.9% saline solution (first insult) was poured into the sample through a funnel about 1.5 "away from the top of the sample center. The sample was allowed to stand for 20 minutes. Pressurized to a circular weight at the top, and after 2 minutes, the wet filter paper was removed and weighed again, with 10 ml saline and 16 filter papers and 10 ml and 20 filter papers for third insult. The procedure was repeated The rewet values and percent fluid retention for the first, second and third insults were calculated according to the following equation: [54] Rewet 1,2, or 3 = wet filter paper weight-dry filter paper weight [55] Retention% = (50-rewet) 50 x 100% [56] In addition, the size of the fluid stain was recorded after the third insult in the fluid retention test. The results are shown in Table 4. [57] Collection Rate and Fluid Retention Test sampleCollection rate (ml / sec)Fluid retention (%)Stain areaFirst Insult2nd Insult3rd InsertFirst Insult2nd Insult3rd Insertcm 2Example 1-MJ998-MF-173.71.61.499%97%86%112 Example 2-MJ998-MF-18b7.56.14.999%91%73%79 Example 3-MJ998-MF-95.43.52.998%79%55%95 [58] Comparing MF-9 and MF-17, when moving the fluid distribution layer from the middle (in the case of MF-9) to the lower part of the three-layer structure (in the case of MF17), the fluid collection rate is reduced to significantly increase the fluid retention. Increase, and fluid stain size increases. [59] The dual compression embodiment (MF-18b) of the present invention is improved over MF-9 in terms of fluid collection rate, fluid retention, and stain size. [60] Additional Example [61] In the following examples, raw materials are as follows unless otherwise noted: [62] Standard fluff pulp: Foley Fluff, Buckeye Technologies Inc., Memphis, TN [63] Elastic fluff pulp: HPF (Buckeye Technologies Inc., Memphis, TN) [64] Compressed fluff pulp: ND416 (Weyerhaeuser-Tacoma, WA) [65] Super Absorbent Powder: 1180 (Stockhausen-Greensboro, NC) [66] Binder Fiber: T-255, 2.8 dtex X 4 mm (Kosa, Charlotte, NC) [67] PET Fiber: T-224, 17 dtex X 6 mm (Kosa, Charlotte, NC) [68] Latex Binder: Airflex 192 (Air Products, Allentown, PA) [69] For the above composition materials, unless otherwise stated, fluid collection tests and fluid retention tests as described above were performed. [70] Examples 4 and 5 -Collection layer matrix fiber [71] Examples 4 and 5 compare latex bonded fluff cellulose fibers and latex bonded synthetic fibers in the collection layer of the composition absorbent structure. [72] Example BU124-19 is one embodiment of the invention using a latex bonded PET fiber collection layer, and BU124-22 is identical to BU124-19 except that the collection layer consists of latex bonded standard fluff cellulose fibers. [73] Absorbent Structure with Latex Binder in Collecting Layer-Example BU12422Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 ) total Compressed pulp69.30.00.069.318.8% Elastic pulp0.043.70.043.727.0% SAP powder0.055.90.055.923.0% Binder fiber6.27.60.013.86.4% PET fiber0.00.00.00.00.0% Standard fluff pulp0.00.038.438.415.8% Latex binder0.00.06.86.82.8% Carrier Tissue15.00.00.015.06.2%total90.5107.245.2242.9100.0% [74] Absorbent Structure without Latex Binder in Collecting Layer-Example BU124-19Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 ) total Compressed pulp69.30.00.069.318.8% Elastic pulp0.043.70.043.727.0% SAP powder0.055.90.055.923.0% Binder fiber6.27.60.013.96.4% PET fiber0.00.038.438.40.0% Standard fluff pulp0.00.00.00.015.8% Latex binder0.00.06.86.82.8% Carrier Tissue15.00.00.015.06.2%total90.5107.245.2243100.0% [75] Table A3 shows the relative fluid collection and retention performance of Samples BU124-22 (with latex bound standard cellulose fluff collection layer) and BU124-19 (with latex bound PET fiber collection layer). [76] Relative performance of absorbent structure with latex binder (BU124-22) and absorbent structure without latex binder (BU124-19) in the collection layer RatingFluid Retention-7ml InsulationThird insult with a collection rate of 5 mlFirst Insult2nd Insult3rd Insert(ml / sec) BU124-2274.1%52.8%38.1%0.053 BU124-1995.6%71.5%56.1%0.18 [77] Examples 6 and 7 -SAP in the middle layer to SAP in the lower layer of a three-layer monostructure [78] Examples 6 and 7 compare the absorbent structures with SAP in the middle layer of the three-layer monostructure versus the absorbent structures with SAP in the lower layer. [79] Example X575 is a preferred embodiment of the invention with SAP in the middle layer; Example X572 is similar to X575 except that the superabsorbent powder is located in the lower layer. [80] Absorbent Structure with SAP in Interlayer-Example X575Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp69.30.00.069.318.8% Elastic pulp0.043.70.043.727.0% SAP powder0.055.90.055.923.0% Binder fiber6.27.60.013.96.4% PET fiber0.00.038.438.415.8% Latex binder0.00.06.86.82.8% Carrier Tissue15.00.00.015.06.2%total90.5107.245.2243100.0% density0.133 gr / cc [81] Absorbent Structure with SAP Underlayer—Example X572Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp45.80.00.045.818.8% Elastic pulp0.065.60.065.627.0% SAP powder55.90.00.055.923.0% Binder fiber7.67.90.015.66.4% PET fiber0.00.038.438.415.8% Latex binder0.00.06.86.82.8% Carrier Tissue15.00.00.015.06.2%total124.373.545.2243.1100.0% density0.114 gr / cc [82] Table B3 shows the fluid collection and retention performance of samples X575 and X572. [83] Relative Performance of Absorbent Structure with SAP in Lower (X572) and Middle (X575) Layers sampleFluid Retention-7ml InsulationThird insult with a collection rate of 5 mlFirst Insult2nd Insult3rd Insert(ml / sec) X57299.1%72.3%48.1%0.171 X57599.0%90.4%66.6%0.255 [84] Examples 8 and 9 Thin sanitary pads on the market versus preferred embodiments [85] Examples 8 and 9 compare some of the preferred absorbent structures of this application with commercially available thin sanitary pads. [86] Examples X573 and X574 are preferred embodiments of the present invention. They differ only in basis weight from sample X575. [87] Three Layer Absorbent Structure-Example X573Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp45.50.00.045.526.0% Elastic pulp0.031.50.031.518.0% SAP powder0.040.30.040.323.0% Binder fiber4.55.50.010.05.7% PET fiber0.00.027.727.715.8% Latex binder0.00.04.94.92.8% Carrier Tissue15.00.00.015.08.6%total65.077.332.6174.9100% density0.105gr / cc [88] Three Layer Absorbent Structure-Example X574Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp59.60.00.059.627.777 Elastic pulp0.038.70.038.718.0% SAP powder0.049.50.049.523.0% Binder fiber5.56.70.012.35.7% PET fiber0.00.034.034.015.8% Latex binder0.00.06.06.02.8% Carrier Tissue15.00.00.015.07.0%total80.194.940.0215.1100.0% density0.124gr / cc [89] Table C3 shows the fluid collection and retention performance of preferred embodiments of the present invention versus commercially available thin sanitary pads. [90] Examples Relative Performance of X573, X574, X575 and Commercially Available Thin Sanitary Pads sampleBasic weightFluid Retention-7ml InsulationCollection Rate 5ml 3rd Insult(gsm)First Insult2nd Insult3rd Insert(ml / sec) X57317095.6%62.7%42.4%0.164 X57421598.9%79.4%57.1%0.195 X57524399.0%90.4%66.6%0.255 brandA36880.0%58.6%44.3%0.040 B23387.1%68.6%51.4%0.068 C25081.4%58.6%38.6%0.018 [91] Examples 10 and 11 Chemically modified fluff cellulose vs. standard fluff cellulose [92] Examples 10 and 11 compare the structures comprising chemically modified fluff cellulose and standard fluff cellulose for the distribution layer. [93] Absorbent Structure with Standard Fluff Cellulose-Example MJ299-MF-2Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 ) total Compressed pulp61.80.00.061.828.2% Elastic pulp0.00.00.00.027.0% Standard pulp0.055.00.055.027.0% SAP powder0.040.00.040.023.0% Binder fiber3.35.00.08.36.4% PET fiber0.00.034.034.015.8% Latex binder0.00.06.06.02.8% Carrier Tissue15.00.00.015.06.2%total80.1100.040.0220.1100.0% density0.127gr / cc [94] Absorbent Structure with Elastic Cellulose Pulp-Example MJ299-MF-6Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp61.80.00.061.828.1% Elastic pulp0.055.00.055.027.0% Standard pulp0.00.00.00.027.0% SAP powder0.040.00.040.023.0% Binder fiber3.35.00.08.36.4% PET fiber0.00.034.034.015.8% Latex binder0.00.06.06.02.8% Carrier Tissue15.00.00.015.06.2%total80.1100.040.0220.1100.0% density0.126 g / cc [95] Table D3 shows the fluid collection and retention performance for samples MJ299-MF-2 and MJ299-MF-6. The test procedure used in Table D3 differs from the MQ3RD023 fluid collection and MQ3RD022 fluid retention procedures in that multiple 10 ml insults of 0.9% saline solution are used in the fluid collection and retention test. [96] Relative Performance of Absorbent Structures with Standard Fluff Cellulose (MJ299-MF-2) and Elastic Cellulose Pulp (MJ299-MF-6) RatingFluid Retention-7ml InsulationCollection Rate 5ml 3rd InsultFirst Insult2nd Insult3rd Insert(ml / sec) MJ299-MF-298.6%76.6%42.8%0.9 MJ299-MF-698.8%73.9%72.0%1.5 [97] Example 12 Preferred Embodiments vs. Commercial Baby Diapers [98] Example 12 compares some preferred absorbent structures of this application with commercially available baby diapers. [99] Example MJ998-HMF-3 is one embodiment of the present invention designed for baby diaper core / collection layer replacement. [100] Absorbent Structures Suitable for Use in Diapers-Example MJ998-HMF-3Distribution layerStorage layerCollection layerSum bottomMiddle sectionTop (g / m 2 )(g / m 2 )(g / m 2 )(g / m 2 )total Compressed pulp95.00.00.095.020.4% Elastic pulp0.00.00.00.00.0% Standard pulp0.0105.00.0105.022.6% SAP powder0.0180.00.0180.038.7% Binder fiber5.015.00.020.04.3% PET fiber0.00.042.542.59.1% Latex binder0.00.08.08.01.7% Carrier Tissue15.00.00.015.03.2%total115.0300.050.5465.5100.0% density0.122gr / cc [101] Table E2 shows the fluid collection rate and fluid retention test results for sample MJ998-HMF-3 and several commercially available diapers. The test procedure is similar to the other examples except that all fluid insults were 50 ml of 0.9% saline and MJ998-NHF-3 was cut into 10 cm × 25 cm sections. [102] Example Performance of MJ998-HMF-3 Multi 50ml Saline Insulation sampleBasic weightFluid retention (%)Holding speed (ml / sec) MJ998-HMF-3(gsm) 477First insult 99.9%Second insult 99.9%3rd Insert 99.5%Third insert 3.7 Commercially available D62299.9%96.8%79.8%2.4 E on the market79299.9%99.0%95.9%1.8 Commercially available F52299.5%96.9%87.3%2.9 G on the market84096.4%79.1%57.2%2.5 [103] Example 13 [104] Compressive forcePETHPFPauli FluffND-416 0 PSI0.0700.0320.0320.038 450 PSI0.0940.0990.1000.113 900 PSI0.1000.1170.1260.170 1350 PSI0.1050.1330.1610.198 [105] Table F compares the response of various fluff cellulose fibers and PET fibers to a given compressive force. The fibers in Table F include 15 denier X 6 mm X 4 crimp / inch PET fibers from Kosa (Salisbury, NC); Chemically modified fluff cellulose fibers, HPF from Buckeye Technologies; Standard fluff cellulose fibers, Pauli fluff, manufactured by Birkeye Technologies; ND-416, a chemically flexible fluff cellulose fiber manufactured by Weyerhaeuser, Tacoma, WA. [106] A mixture containing 90 gsm of each fiber sample with 10 gsm T-255 binder fibers was unfolded and air formed into a 100 gsm fiber batt. Fiber batts were combined in a hot air oven. Separate pieces of each material were pressed for 1 minute with pressing force of 0 psi, 450 psi, 900 psi and 1350 psi. Each compressed sample was measured with a caliper to determine the density. The density is shown in Table F as a measure of the compressive force. From this table it can be seen that various fibers produce bonded airlaid materials with different densities depending on the compressive force applied. [107] Thus, a compressed monostructure consisting of PET fibers, an intermediate layer of Buckeye HPF fibers, and a lower layer of WireHauser ND-416 fibers will not have a constant density from top to bottom. The data shown in Table F shows that the three-layer density gradient is a compressed structure in which the upper PET layer has the lowest density and the lower layer of ND-416 has the highest density.
权利要求:
Claims (57) [1" claim-type="Currently amended] a. A fluid collection layer; b. A fluid distribution layer; And c. A fluid storage layer between the collection layer and the distribution layer, And wherein said collection layer, distribution layer and storage layer are in fluid transfer relationship with each other. [2" claim-type="Currently amended] The method of claim 1, (a) the fluid collection layer comprises polyester fibers and has a basis weight of 20 to 120 gsm; (b) the fluid storage layer comprises 10 to 75% by weight of superabsorbent polymer and has a basis weight of 60 to 400 gms; (c) wherein said fluid distribution layer comprises cellulose fibers and has a basis weight of 20 to 200 gsm. [3" claim-type="Currently amended] A diaper comprising the single absorbent structure of claim 1. [4" claim-type="Currently amended] Feminine hygiene pad comprising the single absorbent structure of claim 1. [5" claim-type="Currently amended] An adult incontinence pad comprising the single absorbent structure of claim 1. [6" claim-type="Currently amended] The method of claim 1, And wherein the average elasticity of each layer decreases in a gradient in the direction of the distribution layer in the collection layer. [7" claim-type="Currently amended] The method of claim 1, And wherein the average pore size of each layer decreases with a gradient in the direction of the distribution layer in the collection layer. [8" claim-type="Currently amended] The method of claim 1, A single absorbent structure, wherein said collection layer comprises an aqueous latex binder resin, bicomponent fibers or mixtures thereof. [9" claim-type="Currently amended] The method of claim 1, A single absorbent structure, wherein said collection layer comprises latex and synthetic fibers. [10" claim-type="Currently amended] The method of claim 1, And wherein said collection layer comprises synthetic fibers and further comprises a binder selected from the group consisting of bicomponent fibers, polyolefin powders, and mixtures thereof. [11" claim-type="Currently amended] The method of claim 1, And wherein said collection layer comprises polyester terephthalate (PET) fibers of at least 2 denier in size. [12" claim-type="Currently amended] The method of claim 1, Wherein said collection layer comprises 3-15 denier crimp PET fibers having a cut length of about 3 to about 12 mm. [13" claim-type="Currently amended] The method of claim 1, And said collection layer comprises a first layer comprising cellulose fibers and a second layer comprising synthetic fibers, said first layer being closer to the storage layer than the second layer. [14" claim-type="Currently amended] The method of claim 1, Wherein said storage layer and distribution layer each comprise thermoplastic bonded fibers. [15" claim-type="Currently amended] The method of claim 1, And said storage layer comprises cellulose fibers and superabsorbent polymer. [16" claim-type="Currently amended] The method of claim 1, Wherein said storage layer comprises cellulose fibers modified to increase the curl and / or stiffness of the fibers. [17" claim-type="Currently amended] The method of claim 1, And wherein the mean pore size of the distribution layer is less than the mean pore size of the collection layer and less than or equal to the mean pore size of the storage layer. [18" claim-type="Currently amended] The method of claim 1, And wherein the mean pore size of said distribution layer is less than the mean pore size of said collection or storage layer. [19" claim-type="Currently amended] The method of claim 1, And wherein the mean pore size of the distribution layer is less than half of the mean pore size of the collection layer and the storage layer. [20" claim-type="Currently amended] The method of claim 1, And wherein said distribution layer comprises cellulose fibers. [21" claim-type="Currently amended] The method of claim 1, And wherein said distribution layer comprises cellulose fibers modified to reduce the stiffness of the fibers. [22" claim-type="Currently amended] The method of claim 1, And a tissue layer in contact with the surface of the distribution layer facing the storage layer. [23" claim-type="Currently amended] a. Airlaying a first batt of fiber to be used for fluid distribution; b. Airlaying a second batt of fiber and superabsorbent material to be used for fluid storage over the first batt of fiber; c. Airlaying a third batt of fiber to be used for fluid collection over the second batt of the fiber; d. Compressing the bat of fibers to form a multilayer absorbent structure comprising a fluid storage layer between the collection layer and the distribution layer. [24" claim-type="Currently amended] The method of claim 23, wherein And applying a latex binder resin to the third batt of said fluid collection layer or fiber. [25" claim-type="Currently amended] The method of claim 23, wherein And wherein said third batt of said fiber comprises synthetic fibers. [26" claim-type="Currently amended] The method of claim 23, wherein And wherein said third batt of said fiber comprises PET fibers having a size of at least 2 denier. [27" claim-type="Currently amended] The method of claim 23, wherein And wherein the third batt of the fiber comprises 3 to 15 denier crimp PET fibers having a cut length of about 3 to about 12 mm. [28" claim-type="Currently amended] The method of claim 23, wherein And wherein said third batt of said fiber comprises cellulose fibers. [29" claim-type="Currently amended] The method of claim 23, wherein And the second batt of the fiber comprises cellulose fiber. [30" claim-type="Currently amended] The method of claim 23, wherein And the second batt of the fiber comprises cellulose fiber modified to increase the curl and stiffness of the fiber. [31" claim-type="Currently amended] The method of claim 23, wherein And wherein said thermoplastic binding fibers are mixed with the first and second batt of fibers during airlaying. [32" claim-type="Currently amended] The method of claim 23, wherein And the first batt of the fiber is compressed to form a distribution layer having a density of about 0.08 to about 0.20 gr / cc before the second batt of the fiber is airlayed. [33" claim-type="Currently amended] The method of claim 23, wherein Compression of the step (d) results in a distribution layer having a density greater than that of the collection and storage layers. [34" claim-type="Currently amended] The method of claim 23, wherein And as a result of the compression of step (d), a distribution layer having a density of at least twice the total density of the collection layer and the storage layer. [35" claim-type="Currently amended] The method of claim 23, wherein Wherein said first batt of said fiber comprises cellulose fibers. [36" claim-type="Currently amended] The method of claim 23, wherein Wherein said first batt of fibers comprises cellulose fibers modified to reduce the stiffness of the fibers. [37" claim-type="Currently amended] The method of claim 23, wherein And as a result of the compression of step (d), a distribution layer having an average pore size that is less than the average pore size of the collection layer and less than or equal to the average pore size of the storage layer. [38" claim-type="Currently amended] The method of claim 23, wherein And the airlay of step (a) is over a tissue layer. [39" claim-type="Currently amended] a. Airlaying a first batt of fiber to be used for fluid distribution; b. Airlaying a second batt of fiber and superabsorbent material to be used for fluid storage over the first batt of fiber; c. Airlaying a third batt of fiber comprising cellulose fiber to be used for fluid collection over the second batt of fiber; d. Airlaying a fourth batt of fiber comprising synthetic fibers to be used for fluid collection over the third batt of fiber; e. Compressing the fibers to form a multi-layer absorbent structure comprising from top to bottom a collection layer comprising synthetic fibers, a collection layer comprising cellulose fibers, a fluid storage layer, and a fluid distribution layer Way. [40" claim-type="Currently amended] The method of claim 39, And said fourth batt of said fiber comprises synthetic fibers. [41" claim-type="Currently amended] The method of claim 39, Applying the latex binder resin to the fluid collection layers of the third and fourth batts of the fiber. [42" claim-type="Currently amended] The method of claim 39, And wherein said third batt of said fiber comprises synthetic fibers. [43" claim-type="Currently amended] The method of claim 39, And wherein said fourth batt of said fiber comprises PET fibers having a size of at least two deniers. [44" claim-type="Currently amended] The method of claim 39, And wherein the fourth batt of the fiber comprises 3 to 15 denier crimped PET fibers having a cut length of about 3 to about 12 mm. [45" claim-type="Currently amended] The method of claim 39, And wherein said third batt of said fiber comprises cellulose fibers. [46" claim-type="Currently amended] The method of claim 39, And the second batt of the fiber comprises cellulose fiber. [47" claim-type="Currently amended] The method of claim 39, And the second batt of the fiber comprises cellulose fiber modified to increase the curl and stiffness of the fiber. [48" claim-type="Currently amended] The method of claim 39, Characterized in that the thermoplastic binding fibers are mixed with the first and second batt of cellulose fibers during airlaying. [49" claim-type="Currently amended] The method of claim 39, And wherein the first batt of the fiber is compressed to form a distribution layer having a density of about 0.08 to about 0.20 gr / cc before the second batt of cellulose fiber is airlayed. [50" claim-type="Currently amended] The method of claim 39, And as a result of the compression of step (e), obtaining a distribution layer having a density greater than that of the collection layer and the storage layer. [51" claim-type="Currently amended] The method of claim 39, And as a result of the compression of step (e), obtaining a distribution layer having a density that is at least twice the total density of the collection layer and the storage layer. [52" claim-type="Currently amended] The method of claim 39, Wherein said first batt of said fiber comprises cellulose fibers. [53" claim-type="Currently amended] The method of claim 39, Wherein said first batt of fibers comprises cellulose fibers that have been chemically modified to increase the curl and thickness of the fibers. [54" claim-type="Currently amended] The method of claim 39, As a result of the compression of step (e), obtaining a distribution layer having an average pore size that is less than the average pore size of the collection layer and less than or equal to the average pore size of the storage layer. [55" claim-type="Currently amended] The method of claim 39, The airlay of step (a) is over a tissue layer. [56" claim-type="Currently amended] a. Airlaying a first batt of fiber to be used for fluid distribution; b. Airlaying a second batt of fiber to be used for fluid storage over the first batt of the fiber; c. Airlaying a superabsorbent material over the second batt of the fiber; d. Airlaying a third batt of fiber to be used for fluid collection over the second batt of the fiber; e. Compressing the fibers to form a multi-layer absorbent structure comprising a fluid storage layer between the collection layer and the distribution layer. [57" claim-type="Currently amended] a. Airlaying a first batt of fiber to be used for fluid distribution; b. Airlaying a second batt of fiber to be used for fluid storage over the first batt of the fiber; c. Airlaying a superabsorbent material over the second batt of the fiber; d. Airlaying a third batt of fiber to be used for fluid collection over the second batt of the fiber; e. Airlaying a fourth batt of fiber to be used for fluid collection over the third batt of the fiber; And f. Compressing the fibers to form a layered absorbent structure comprising, from top to bottom, a collection layer comprising synthetic fibers, a collection layer comprising cellulose fibers, a fluid storage layer, and a fluid distribution layer. Method of formation.
类似技术:
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同族专利:
公开号 | 公开日 JP2012125597A|2012-07-05| JP2003518958A|2003-06-17| ES2270745T1|2007-04-16| EP2184042B1|2018-10-24| CN1191044C|2005-03-02| DE00948502T1|2004-05-19| BR0012306B1|2010-12-14| DE20024022U1|2010-04-22| US6420626B1|2002-07-16| CN1358080A|2002-07-10| CA2632700A1|2000-12-14| WO2000074620A1|2000-12-14| EP1191915B1|2011-10-12| EP2184042A2|2010-05-12| AU761200B2|2003-05-29| CA2632700C|2013-01-29| JP5404835B2|2014-02-05| BR0012306A|2002-05-14| MXPA01012660A|2002-06-04| EP1191915A1|2002-04-03| ES2270745T3|2012-02-22| CA2376369C|2008-09-09| JP4995386B2|2012-08-08| US20020165509A1|2002-11-07| US8105301B2|2012-01-31| AT527972T|2011-10-15| EP1191915A4|2006-03-15| AU6198200A|2000-12-28| WO2000074620A9|2002-06-27| EP2184042A3|2010-12-22| CA2376369A1|2000-12-14|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
法律状态:
1999-06-08|Priority to US09/325,764 1999-06-08|Priority to US09/325,764 2000-06-08|Application filed by 비케이아이 홀딩 코포레이션 2000-06-08|Priority to PCT/US2000/016001 2002-05-30|Publication of KR20020040674A 2012-07-12|First worldwide family litigation filed
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申请号 | 申请日 | 专利标题 US09/325,764|US6420626B1|1999-06-08|1999-06-08|Unitary fluid acquisition, storage, and wicking material| US09/325,764|1999-06-08| PCT/US2000/016001|WO2000074620A1|1999-06-08|2000-06-08|Unitary fluid acquisition, storage, and wicking material| 相关专利
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