US20170009401A1 - Fibrous Structures and Methods for Making Same - Google Patents

Fibrous Structures and Methods for Making Same Download PDF

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Publication number
US20170009401A1
US20170009401A1 US15/202,799 US201615202799A US2017009401A1 US 20170009401 A1 US20170009401 A1 US 20170009401A1 US 201615202799 A US201615202799 A US 201615202799A US 2017009401 A1 US2017009401 A1 US 2017009401A1
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United States
Prior art keywords
fibrous
fibrous structure
less
filaments
present
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US15/202,799
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English (en)
Inventor
Janese Christine O'Brien Stickney
Brooke Marie Woods
Sharon Rae Antoun
David William Cabell
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Procter and Gamble Co
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Procter and Gamble Co
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Priority to US15/202,799 priority Critical patent/US20170009401A1/en
Assigned to THE PROCTER & GAMBLE COMPANY reassignment THE PROCTER & GAMBLE COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: O'BRIEN STICKNEY, JANESE CHRISTINE, CABELL, DAVID WILLIAM, WOODS, BROOKE MARIE, ANTOUN, SHARON RAE
Publication of US20170009401A1 publication Critical patent/US20170009401A1/en
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    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/002—Tissue paper; Absorbent paper
    • D21H27/004—Tissue paper; Absorbent paper characterised by specific parameters
    • D21H27/005—Tissue paper; Absorbent paper characterised by specific parameters relating to physical or mechanical properties, e.g. tensile strength, stretch, softness
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D21H11/02—Chemical or chemomechanical or chemothermomechanical pulp
    • D21H11/04—Kraft or sulfate pulp
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H13/00—Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/10—Organic non-cellulose fibres
    • D21H13/28—Organic non-cellulose fibres from natural polymers
    • D21H13/30—Non-cellulose polysaccharides
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H15/00—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution
    • D21H15/02—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution characterised by configuration
    • D21H15/06—Long fibres, i.e. fibres exceeding the upper length limit of conventional paper-making fibres; Filaments
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/002—Tissue paper; Absorbent paper
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/002—Tissue paper; Absorbent paper
    • D21H27/004—Tissue paper; Absorbent paper characterised by specific parameters
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/30—Multi-ply

Definitions

  • the present invention relates to fibrous structures and more particularly to fibrous structures that exhibit improved surface properties, such as softness, compared to known fibrous structures and methods for making such novel fibrous structures.
  • Formulators in the past have imparted crepe to a surface of the fibrous structure, such as by creping the fibrous structure off a dryer or Yankee and/or by other means of foreshortening the fibrous structure, such as rush transfer steps in making the fibrous structure, to improve softness of fibrous structure the exterior surfaces of a sanitary tissue product comprising the creped fibrous structure.
  • Formulators have tried to utilize the EMTEC Tissue Softness Analyzer from Emtec Electronic GmbH of Leipzig, Germany to measure the softness (TS7) of creped fibrous structures and/or surface smoothness (TS750) of the creped surfaces of the sanitary tissue products.
  • examples of single- and/or multi-ply fibrous structures such as sanitary tissue product, comprising a plurality of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments such as starch filaments and/or hydroxyl polymer fibers such as cellulose fibers, such as wood pulp fibers, wherein the fibrous structures comprise uncreped exterior surfaces exhibit TS7 values and/or TS 750 values as measured according to the Emtec Test Method described herein (which defines the calibration method used) that are higher (for example less soft) than desired by consumers and/or formulators of such fibrous structures.
  • hydroxyl polymer fibrous elements for example hydroxyl polymer filaments such as starch filaments and/or hydroxyl polymer fibers such as cellulose fibers, such as wood pulp fibers
  • the fibrous structures comprise uncreped exterior surfaces exhibit TS7 values and/or TS 750 values as measured according to the Emtec Test Method described herein (which defines the calibration method used) that are higher (for example less soft) than desired by consumers and/or
  • Dry surface feel of fibrous structures is an important factor in a consumer's purchasing decisions when choosing to purchase sanitary tissue products.
  • the higher the average TS7 values as measured according to the Emtec Test Method described herein the less soft the fibrous structure feels to a consumer of such a fibrous structure.
  • the known fibrous structures may exhibit wet feel deficiencies.
  • the basis weight of hydroxyl polymer fibrous elements present in an exterior layer and/or on an exterior surface of the known fibrous structure is critical because too high a basis weight (greater than 6 and/or greater than 8 and/or greater than 10 gsm) of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments, in an exterior layer and/or on an exterior surface of the known fibrous structure creates a gooey feel during use.
  • hydroxyl polymer fibrous elements for example the type of hydroxyl polymer and/or the effectiveness of the crosslinking of the hydroxyl polymer, which relates at least partially to the level of base such as triethanolamine present in the crosslinking agent used to make the hydroxyl polymer fibrous elements.
  • base such as triethanolamine present in the crosslinking agent used to make the hydroxyl polymer fibrous elements.
  • crosslinking agents used to make known fibrous structures comprising hydroxyl polymer filaments comprised 2% by weight or more of base.
  • the known fibrous structures comprising an exterior layer and/or exterior surface comprising hydroxyl polymer filaments have a level of hydroxyl polymer filaments in the exterior layer and/or on the exterior surface of about 2 to 3 gsm.
  • fibrous structures for example fibrous structures comprising a plurality of hydroxyl polymer fibrous elements such as hydroxyl polymer filaments and/or hydroxyl polymer fibers, is that such fibrous structures exhibit average TS7 and/or TS750 values as measured according to the Emtec Test Method described herein that are higher than desired by consumers of such fibrous structures.
  • fibrous structures for example fibrous structures comprising hydroxyl polymer fibrous elements such as hydroxyl polymer filaments and/or hydroxyl polymer fibers, that exhibit improved surface properties, for example improved dry surface feel properties such as lower average TS7 and/or TS750 values as measured according to the Emtec Test Method described herein than the fibrous structures, and methods for making such fibrous structures.
  • hydroxyl polymer fibrous elements such as hydroxyl polymer filaments and/or hydroxyl polymer fibers
  • improved surface properties for example improved dry surface feel properties such as lower average TS7 and/or TS750 values as measured according to the Emtec Test Method described herein than the fibrous structures, and methods for making such fibrous structures.
  • the present invention fulfills the needs described above by providing fibrous structures and single- or multi-ply sanitary tissue products comprising such fibrous structures, for example fibrous structures and/or single- or multi-ply sanitary tissue products that exhibit improved surface properties, such as softness, as measured according to the Emtec Test Method described herein, and more particularly to such fibrous structures and/or single- or multi-ply sanitary tissue products comprising at least one uncreped exterior surface and/or that comprise a plurality of hydroxyl polymer fibrous elements, such as hydroxyl polymer filaments, which may be present in an exterior layer and/or on an exterior surface of the fibrous structures and/or sanitary tissue products, that exhibit improved surface properties compared to known fibrous structures, for example known fibrous structures comprising a plurality of hydroxyl polymer fibrous elements, and methods for making such fibrous structures and/or sanitary tissue products.
  • fibrous structures and/or sanitary tissue products comprising such fibrous structures, for example fibrous structures and/or sanitary tissue products comprising at least one uncreped exterior surface and/or comprising a plurality of hydroxyl polymer fibrous elements such as hydroxyl polymer filaments such as starch filaments on at least one exterior surface of the fibrous structure, and/or hydroxyl polymer fibers such as cellulose fibers, for example wood pulp fibers, such that the fibrous structures exhibit average TS7 and/or TS750 values as measured according to the Emtec Test Method described herein that are lower than known fibrous structures.
  • hydroxyl polymer fibrous elements such as hydroxyl polymer filaments such as starch filaments on at least one exterior surface of the fibrous structure
  • hydroxyl polymer fibers such as cellulose fibers, for example wood pulp fibers
  • the improved surface feel is attributable to features of the polymer melt composition as described herein, for example the type of hydroxyl polymer and/or the effectiveness of the crosslinking of the hydroxyl polymer, which relates at least partially to the level of base such as triethanolamine present in the crosslinking agent used to make the hydroxyl polymer fibrous elements, for example less than 2% and/or less than 1.8% and/or less than 1.5% and/or less than 1.25% and/or about 0% and/or about 0.25% and/or about 0.5% by weight, to produce the hydroxyl polymer fibrous elements, the average diameters of the hydroxyl polymer fibrous elements, for example less than 50 ⁇ m and/or less than 25 ⁇ m and/or less than 10 ⁇ m and/or less than 8 ⁇ m and/or less than 6 ⁇ m as measured according to the Average Diameter Test Method described herein, and associated processing conditions, such as thermal bonding of the fibrous structures, for example such that the Dry Pill Area value is less than 5% and
  • a fibrous structure and/or sanitary tissue product comprising a fibrous structure comprising at least one uncreped exterior surface, for example a consumer-contacting surface, in other words, a surface that contacts a consumer during use, comprising a plurality of filaments and fibers, wherein the fibrous structure comprises at least one uncreped exterior surface such that the fibrous structure exhibits an average TS7 value of less than 6.25 dB V 2 rms as measured according to the Emtec Test Method, is provided.
  • a fibrous structure and/or sanitary tissue product comprising a fibrous structure comprising a plurality of hydroxyl polymer filaments that are present in at least one exterior layer of the fibrous structure at a level of greater than 5 gsm such that the fibrous structure exhibits an average TS7 value of less than 10.00 dB V 2 rms as measured according to the Emtec Test Method, is provided.
  • a fibrous structure and/or sanitary tissue product comprising a fibrous structure comprising a plurality of fibers and at least one uncreped exterior surface, for example a consumer-contacting surface, in other words, a surface that contacts a consumer during use, such that the fibrous structure exhibits an average TS7 value of less than 6.25 dB V 2 rms as measured according to the Emtec Test Method, is provided.
  • a single- or multi-ply sanitary tissue product for example bath tissue, comprising a fibrous structure of the present invention.
  • the present invention provides novel fibrous structures that exhibit novel average TS7 values and/or novel average TS750 values as measured according to the Emtec Test Method described herein and methods for making such fibrous structures.
  • FIG. 1 is a schematic representation of one example of a method for making a fibrous structure according to the present invention
  • FIG. 2 is a schematic representation of one example of a portion of fibrous structure making process according to the present invention.
  • FIG. 3 is a schematic representation of an example of a meltblow die in accordance with the present invention.
  • Fibrous element as used herein means an elongate particulate having a length greatly exceeding its average diameter, i.e. a length to average diameter ratio of at least about 10.
  • a fibrous element may be a filament or a fiber.
  • the fibrous element is a single fibrous element rather than a yarn comprising a plurality of fibrous elements.
  • the fibrous elements of the present invention may be spun from polymer melt compositions via suitable spinning operations, such as meltblowing and/or spunbonding and/or they may be obtained from natural sources such as vegetative sources, for example trees.
  • the fibrous elements of the present invention may be monocomponent and/or multicomponent.
  • the fibrous elements may comprise bicomponent fibers and/or filaments.
  • the bicomponent fibers and/or filaments may be in any form, such as side-by-side, core and sheath, islands-in-the-sea and the like.
  • “Filament” as used herein means an elongate particulate as described above that exhibits a length of greater than or equal to 5.08 cm (2 in.) and/or greater than or equal to 7.62 cm (3 in.) and/or greater than or equal to 10.16 cm (4 in.) and/or greater than or equal to 15.24 cm (6 in.).
  • Filaments are typically considered continuous or substantially continuous in nature. Filaments are relatively longer than fibers.
  • Non-limiting examples of filaments include meltblown and/or spunbond filaments.
  • Non-limiting examples of polymers that can be spun into filaments include natural polymers, such as starch, starch derivatives, cellulose, such as rayon and/or lyocell, and cellulose derivatives, hemicellulose, hemicellulose derivatives, and synthetic polymers including, but not limited to polyvinyl alcohol, thermoplastic polymer, such as polyesters, nylons, polyolefins such as polypropylene filaments, polyethylene filaments, and biodegradable thermoplastic fibers such as polylactic acid filaments, polyhydroxyalkanoate filaments, polyesteramide filaments and polycaprolactone filaments.
  • Fiber as used herein means an elongate particulate as described above that exhibits a length of less than 5.08 cm (2 in.) and/or less than 3.81 cm (1.5 in.) and/or less than 2.54 cm (1 in.).
  • Fibers are typically considered discontinuous in nature.
  • fibers include pulp fibers, such as wood pulp fibers, and synthetic staple fibers such as polypropylene, polyethylene, polyester, copolymers thereof, rayon, glass fibers and polyvinyl alcohol fibers.
  • Staple fibers may be produced by spinning a filament tow and then cutting the tow into segments of less than 5.08 cm (2 in.) thus producing fibers.
  • a fiber may be a naturally occurring fiber, which means it is obtained from a naturally occurring source, such as a vegetative source, for example a tree and/or plant, such as trichomes.
  • a naturally occurring source such as a vegetative source, for example a tree and/or plant, such as trichomes.
  • Such fibers are typically used in papermaking and are oftentimes referred to as papermaking fibers.
  • Papermaking fibers useful in the present invention include cellulosic fibers commonly known as wood pulp fibers. Applicable wood pulps include chemical pulps, such as Kraft, sulfite, and sulfate pulps, as well as mechanical pulps including, for example, groundwood, thermomechanical pulp and chemically modified thermomechanical pulp. Chemical pulps, however, may be preferred since they impart a superior tactile sense of softness to fibrous structures made therefrom.
  • Pulps derived from both deciduous trees hereinafter, also referred to as “hardwood”) and coniferous trees (hereinafter, also referred to as “softwood”) may be utilized.
  • the hardwood and softwood fibers can be blended, or alternatively, can be deposited in layers to provide a stratified web.
  • fibers derived from recycled paper which may contain any or all of the above categories of fibers as well as other non-fibrous polymers such as fillers, softening agents, wet and dry strength agents, and adhesives used to facilitate the original papermaking.
  • cellulosic fibers such as cotton linters, rayon, lyocell, and bagasse fibers can be used in the fibrous structures of the present invention.
  • Fibrous structure as used herein means a structure that comprises one or more fibrous elements.
  • a fibrous structure according to the present invention means an association of fibrous elements that together form a structure capable of performing a function.
  • a fibrous structure comprises a plurality of inter-entangled fibrous elements, for example filaments.
  • “Sanitary tissue product” as used herein means a soft, relatively low density fibrous structure useful as a wiping implement for post-urinary and post-bowel movement cleaning (toilet tissue), for otorhinolaryngological discharges (facial tissue), multi-functional absorbent and cleaning uses (absorbent towels) and wipes, such as wet and dry wipes.
  • the sanitary tissue product may be convolutedly wound upon itself about a core or without a core to form a sanitary tissue product roll or may be in the form of discrete sheets.
  • the sanitary tissue product of the present invention comprises one or more fibrous structures according to the present invention.
  • the sanitary tissue products and/or fibrous structures of the present invention may exhibit a basis weight between about 1 g/m 2 to about 5000 g/m 2 and/or from about 10 g/m 2 to about 500 g/m 2 and/or from about 10 g/m 2 to about 300 g/m 2 and/or from about 10 g/m 2 to about 120 g/m 2 and/or from about 15 g/m 2 to about 110 g/m 2 and/or from about 20 g/m 2 to about 100 g/m 2 and/or from about 30 to 90 g/m 2 as determined by the Basis Weight Test Method described herein.
  • the sanitary tissue product of the present invention may exhibit a basis weight between about 40 g/m 2 to about 120 g/m 2 and/or from about 50 g/m 2 to about 110 g/m 2 and/or from about 55 g/m 2 to about 105 g/m 2 and/or from about 60 g/m 2 to 100 g/m 2 as determined by the Basis Weight Test Method described herein.
  • the sanitary tissue products of the present invention may exhibit a total dry tensile strength of greater than about 59 g/cm and/or from about 78 g/cm to about 394 g/cm and/or from about 98 g/cm to about 335 g/cm.
  • the sanitary tissue product of the present invention may exhibit a total dry tensile strength of greater than about 196 g/cm and/or from about 196 g/cm to about 394 g/cm and/or from about 216 g/cm to about 335 g/cm and/or from about 236 g/cm to about 315 g/cm.
  • the sanitary tissue product exhibits a total dry tensile strength of less than about 394 g/cm and/or less than about 335 g/cm.
  • the sanitary tissue products of the present invention may exhibit a density of less than 0.60 g/cm 3 and/or less than 0.30 g/cm 3 and/or less than 0.20 g/cm 3 and/or less than 0.15 g/cm 3 and/or less than 0.10 g/cm 3 and/or less than 0.07 g/cm 3 and/or less than 0.05 g/cm 3 and/or from about 0.01 g/cm 3 to about 0.20 g/cm 3 and/or from about 0.02 g/cm 3 to about 0.15 g/cm 3 and/or from about 0.02 g/cm 3 to about 0.10 g/cm 3 .
  • the sanitary tissue products of the present invention may be in the form of sanitary tissue product rolls.
  • Such sanitary tissue product rolls may comprise a plurality of connected, but perforated sheets of fibrous structure, that are separably dispensable from adjacent sheets.
  • the sanitary tissue products of the present invention may comprise additives such as softening agents, temporary wet strength agents, permanent wet strength agents, bulk softening agents, lotions, silicones, wetting agents, latexes, patterned latexes and other types of additives suitable for inclusion in and/or on sanitary tissue products.
  • additives such as softening agents, temporary wet strength agents, permanent wet strength agents, bulk softening agents, lotions, silicones, wetting agents, latexes, patterned latexes and other types of additives suitable for inclusion in and/or on sanitary tissue products.
  • “Scrim” as used herein means a material that is used to overlay solid additives present on and/or within a nonwoven substrate of the fibrous structures of the present invention such that the solid additives are positioned between the scrim and a layer of the fibrous structure.
  • the scrim covers the solid additives such that they are positioned between the scrim and a surface of the nonwoven substrate of the fibrous structure.
  • the scrim is a minor component (for example less than 25% of the basis weight) relative to the nonwoven substrate of the basis weight of the fibrous structure.
  • the scrim forms at least one exterior layer and/or exterior surface of a fibrous structure of the present invention.
  • “Hydroxyl polymer” as used herein includes any hydroxyl-containing polymer that can be incorporated into a filament of the present invention.
  • the hydroxyl polymer of the present invention includes greater than 10% and/or greater than 20% and/or greater than 25% by weight hydroxyl moieties.
  • the hydroxyl within the hydroxyl-containing polymer is not part of a larger functional group such as a carboxylic acid group.
  • Non-thermoplastic as used herein means, with respect to a material, such as a fibrous element as a whole and/or a polymer, such as a crosslinked polymer, within a fibrous element, that the fibrous element and/or polymer exhibits no melting point and/or softening point, which allows it to flow under pressure, in the absence of a plasticizer, such as water, glycerin, sorbitol, urea and the like.
  • a plasticizer such as water, glycerin, sorbitol, urea and the like.
  • Non-cellulose-containing as used herein means that less than 5% and/or less than 3% and/or less than 1% and/or less than 0.1% and/or 0% by weight of cellulose polymer, cellulose derivative polymer and/or cellulose copolymer is present in fibrous element. In one example, “non-cellulose-containing” means that less than 5% and/or less than 3% and/or less than 1% and/or less than 0.1% and/or 0% by weight of cellulose polymer is present in fibrous element.
  • Crosslinking facilitator and/or “crosslinking facilitator function” as used herein means any material that is capable of activating a crosslinking agent thereby transforming the crosslinking agent from its unactivated state to its activated state.
  • “Fast wetting surfactant” and/or “fast wetting surfactant component” and/or “fast wetting surfactant function” as used herein means a surfactant and/or surfactant component, such as an ion from a fast wetting surfactant, for example a sulfosuccinate diester ion (anion), that exhibits a Critical Micelle Concentration (CMC) of greater 0.15% by weight and/or at least 0.25% and/or at least 0.50% and/or at least 0.75% and/or at least 1.0% and/or at least 1.25% and/or at least 1.4% and/or less than 10.0% and/or less than 7.0% and/or less than 4.0% and/or less than 3.0% and/or less than 2.0% by weight.
  • CMC Critical Micelle Concentration
  • Polymer melt composition or “Polysaccharide melt composition” as used herein means a composition comprising water and a melt processed polymer, such as a melt processed fibrous element-forming polymer, for example a melt processed hydroxyl polymer, such as a melt processed polysaccharide.
  • “Melt processed fibrous element-forming polymer” as used herein means any polymer, which by influence of elevated temperatures, pressure and/or external plasticizers may be softened to such a degree that it can be brought into a flowable state, and in this condition may be shaped as desired.
  • melt processed hydroxyl polymer as used herein means any polymer that contains greater than 10% and/or greater than 20% and/or greater than 25% by weight hydroxyl groups and that has been melt processed, with or without the aid of an external plasticizer. More generally, melt processed hydroxyl polymers include polymers, which by the influence of elevated temperatures, pressure and/or external plasticizers may be softened to such a degree that they can be brought into a flowable state, and in this condition may be shaped as desired.
  • “Blend” as used herein means that two or more materials, such as a fibrous element-forming polymer, for example a hydroxyl polymer and a polyacrylamide are in contact with each other, such as mixed together homogeneously or non-homogeneously, within a filament.
  • a filament formed from one material, but having an exterior coating of another material is not a blend of materials for purposes of the present invention.
  • a fibrous element formed from two different materials is a blend of materials for purposes of the present invention even if the fibrous element further comprises an exterior coating of a material.
  • “Associate,” “Associated,” “Association,” and/or “Associating” as used herein with respect to fibrous elements means combining, either in direct contact or in indirect contact, fibrous elements such that a fibrous structure is formed.
  • the associated fibrous elements may be bonded together for example by adhesives and/or thermal bonds.
  • the fibrous elements may be associated with one another by being deposited onto the same fibrous structure making belt.
  • a fibrous element of the present invention exhibits an average diameter of less than 50 ⁇ m and/or less than 25 ⁇ m and/or less than 20 ⁇ m and/or less than 15 ⁇ m and/or less than 10 ⁇ m and/or less than 6 ⁇ m and/or greater than 1 ⁇ m and/or greater than 3 ⁇ m.
  • Basis Weight as used herein is the weight per unit area of a sample reported in lbs/3000 ft 2 or g/m 2 as determined by the Basis Weight Test Method described herein.
  • Machine Direction or “MD” as used herein means the direction parallel to the flow of the fibrous structure through a fibrous structure making machine and/or sanitary tissue product manufacturing equipment. Typically, the MD is substantially perpendicular to any perforations present in the fibrous structure
  • Cross Machine Direction or “CD” as used herein means the direction perpendicular to the machine direction in the same plane of the fibrous structure and/or sanitary tissue product comprising the fibrous structure.
  • Ply or “Plies” as used herein means an individual fibrous structure optionally to be disposed in a substantially contiguous, face-to-face relationship with other plies, forming a multiple ply fibrous structure. It is also contemplated that a single fibrous structure can effectively form two “plies” or multiple “plies”, for example, by being folded on itself.
  • Uncreped exterior surface” and/or “uncreped exterior layer” as used herein means a surface and/or layer of the fibrous structure and/or sanitary tissue product comprising the fibrous structure that has not contacted a Yankee or cylindrical dryer during the fibrous structure making process and/or fibrous structure converting process, and thus has not been creped off a Yankee or cylindrical dryer.
  • “uncreped” means that the fibrous structure has not been foreshortened.
  • component or composition levels are in reference to the active level of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources.
  • the fibrous structures of the present invention comprise a plurality of fibrous elements, for example hydroxyl polymer filaments comprising a hydroxyl polymer such as a crosslinked hydroxyl polymer.
  • the fibrous structures may comprise starch and/or starch derivative filaments.
  • the starch filaments may further comprise polyvinyl alcohol and/or other polymers.
  • the fibrous structures of the present invention may comprise a mixture of different fibrous elements for example a mixture of filaments, for example hydroxyl polymer filaments such as starch filaments, and fibers, for example cellulose fibers such as pulp fibers.
  • the mixture of fibrous elements may comprise a commingled mixture of filaments and fibers and/or a layered association of filaments and fibers such that the fibrous structure exhibits novel average TS7 values and/or novel TS 750 values as measured according to the Emtec Test Method described herein.
  • the fibrous structures of the present invention may be thermally bonded to bond the fibrous elements together to provide the fibrous structure with strength sufficient for its intended use, such as for use as bath tissue, and to control the pills, for example such that the fibrous structure exhibits a Dry Pill Area value of less than 5% and/or less than 4% and/or less than 3% and/or less than 2.5% as measured according to the Lint/Pilling Test Method described herein.
  • the fibrous structure of the present invention comprises a plurality of filaments and fibers, wherein the fibrous structure comprises at least one uncreped exterior surface such that the fibrous structure exhibits an average TS7 value of less than 6.25 and/or less than 6.15 and/or less than 6.00 and/or less than 5.50 and/or less than 5.00 and/or less than 4.75 and/or less than 4.50 and/or less than 4.10 dB V 2 rms and/or less than 6.25 to greater than 0 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structure of the present invention may exhibit an average TS750 value of greater than 6.00 and/or greater than 8.00 and/or greater than 10.00 and/or greater than 20.00 and/or greater than 25.00 and/or less than 100 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structure of the present invention comprises a plurality of hydroxyl polymer filaments that are present in at least one exterior layer of the fibrous structure at a level of greater than 5 gsm and/or greater than 6 gsm and/or greater than 8 gsm and/or greater than 10 gsm and/or greater than 12 gsm and/or greater than 14 gsm and/or greater than 16 gsm and/or greater than 18 gsm such that the fibrous structure exhibits an average TS7 value of less than 10.00 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structure of the present invention comprises a plurality of fibers and at least one uncreped exterior surface such that the fibrous structure exhibits an average TS7 value of less than 6.25 and/or less than 6.15 and/or less than 6.00 and/or less than 5.50 and/or less than 5.00 and/or less than 4.75 and/or less than 4.50 and/or less than 4.10 dB V 2 rms and/or less than 6.25 to greater than 0 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structure of the present invention comprises a layered fibrous structure comprising a least one exterior layer comprising a plurality of hydroxyl polymer filaments present at a level of greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or greater than 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm and another layer of solid additives, such as pulp fibers present at a level of greater than 6 and/or greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or greater than 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm and/or from about 6 to about 40 gsm and/or from about 10 to about 35 gsm and/or from about 12 to about 25 gsm, such that the fibrous structure exhibits one of more of the following average TS7 values and/or average TS750 values as measured according to
  • the fibrous structures of the present invention may comprise a plurality of fibrous elements, for example hydroxyl polymer filaments, such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments, such that the fibrous structures exhibit an average TS7 value of less than 4 db V 2 rms and/or less than 3.7 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • hydroxyl polymer filaments such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments
  • the fibrous structure may exhibit an average TS750 value of greater than 6 dB V 2 rms and/or greater than 8 dB V 2 rms and/or greater than 10 dB V 2 rms and/or greater than 20 dB V 2 rms and/or greater than 25 dB V 2 rms and/or less than 100 dB V 2 rms and/or less than 80 dB V 2 rms and/or less than 60 dB V 2 rms and/or less than 50 dB V 2 rms and/or greater than 25 to less than 50 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • a fibrous structure comprising a plurality of hydroxyl polymer filaments that are present in an exterior layer and/or on an exterior surface of the fibrous structure at a level of greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or at least 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm, such that the fibrous structure exhibits an average TS7 value of less than 10 and/or less than 8 and/or less than 7 and/or less than 6 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structures of the present invention may comprise a plurality of fibrous elements, for example hydroxyl polymer filaments, such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments, such that the fibrous structures exhibit an average TS7 value of less than 4.8 db V 2 rms and/or less than 4.5 db V 2 rms and/or less than 4 db V 2 rms and/or less than 3.5 db V 2 rms and/or less than 3 db V 2 rms and an average TS750 value of greater than 6 dB V 2 rms and/or greater than 8 dB V 2 rms and/or greater than 10 dB V 2 rms and/or greater than 20 dB V 2 rms and/or greater than 25 dB V 2 rms and/or less than 100 dB V 2 rms and/or less than 80 dB V 2 rms and
  • the fibrous structures of the present invention may comprise a plurality of filaments, for example hydroxyl polymer filaments, such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments, such that the fibrous structures exhibit an average TS7 value of less than 6.2 db V 2 rms and/or less than 6 db V 2 rms and/or less than 5.8 db V 2 rms and/or less than 5.6 db V 2 rms and/or less than 5.4 db V 2 rms and/or less than 5.2 db V 2 rms and/or less than 5 db V 2 rms and/or less than 4.7 db V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structure may exhibit an average TS750 value of greater than 6 dB V 2 rms and/or greater than 8 dB V 2 rms and/or greater than 10 dB V 2 rms and/or greater than 20 dB V 2 rms and/or greater than 25 dB V 2 rms and/or less than 100 dB V 2 rms and/or less than 80 dB V 2 rms and/or less than 60 dB V 2 rms and/or less than 50 dB V 2 rms and/or greater than 25 to less than 50 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structures of the present invention may be uncreped fibrous structures comprising a plurality of fibrous elements, for example hydroxyl polymer filaments, such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments, such that the uncreped fibrous structures exhibit an average TS7 value of less than 6.2 db V 2 rms and/or less than 6 db V 2 rms and/or less than 5.8 db V 2 rms and/or less than 5.6 db V 2 rms and/or less than 5.4 db V 2 rms and/or less than 5.2 db V 2 rms and/or less than 5 db V 2 rms and/or less than 4.7 db V 2 rms as measured according to the Emtec Test Method described herein.
  • hydroxyl polymer filaments such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments
  • the fibrous structure may exhibit an average TS750 value of greater than 6 dB V 2 rms and/or greater than 8 dB V 2 rms and/or greater than 10 dB V 2 rms and/or greater than 20 dB V 2 rms and/or greater than 25 dB V 2 rms and/or less than 100 dB V 2 rms and/or less than 80 dB V 2 rms and/or less than 60 dB V 2 rms and/or less than 50 dB V 2 rms and/or greater than 25 to less than 50 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • a fibrous structure comprising a plurality of hydroxyl polymer filaments that are present in an exterior layer and/or on an exterior surface of the fibrous structure at a level of greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or at least 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm, such that the fibrous structure exhibits an average TS7 value of less than 10 and/or less than 8 and/or less than 7 and/or less than 6 dB V 2 rms as measured according to the Emtec Test Method described herein.
  • the fibrous structures of the present invention may comprise a plurality of filaments, for example hydroxyl polymer filaments, such as at least one exterior surface comprising a plurality of hydroxyl polymer filaments, such that the fibrous structures exhibit an average TS7 value, for example less than 10 db V 2 rms and/or less than 9 db V 2 rms and/or less than 8 db V 2 rms and/or less than 7 db V 2 rms and/or less than 6 db V 2 rms and/or less than 5 db V 2 rms and/or less than 4 db V 2 rms and/or less than 3 db V 2 rms, and an average TS750 value, for example greater than 6 dB V 2 rms and/or greater than 8 dB V 2 rms and/or greater than 10 dB V 2 rms and/or greater than 20 dB V 2 rms, and an
  • the fibrous structures of the present invention may exhibit any features of the above described fibrous structures of the present invention and/or may exhibit any combination of average TS7 values and TS750 values as measured according to the Emtec Test Method described herein.
  • any of the fibrous structures described above may comprise at least one and/or two uncreped exterior surfaces, which may be void or substantially void of fibers, for example pulp fibers, such as wood pulp fibers.
  • At least a portion, if not all, of fibers within any of the fibrous structures of the present invention may be positioned interior to at least one uncreped exterior surface of the fibrous structures.
  • the fibrous structure of the present invention may comprise two uncreped exterior surfaces and/or layers. In one example, at least a portion, if not all, of the fibers present in the fibrous structure are positioned between two of the uncreped exterior surfaces of the fibrous structure.
  • the fibrous structures of the present invention may be non-lotioned and/or may not contain a post-applied surface chemistry.
  • the fibrous structures of the present invention may be creped or uncreped.
  • the fibrous structures of the present invention are uncreped fibrous structures.
  • such fibrous structures also may exhibit improved cleaning properties, for example bowel movement cleaning properties, compared to known fibrous structures, for example known fibrous structures comprising hydroxyl polymer filaments and known fibrous structures, such as wet-laid and/or air-laid, comprising cellulose fibers, for example pulp fibers.
  • known fibrous structures comprising hydroxyl polymer filaments and known fibrous structures, such as wet-laid and/or air-laid, comprising cellulose fibers, for example pulp fibers.
  • known fibrous structures comprising hydroxyl polymer filaments and known fibrous structures, such as wet-laid and/or air-laid, comprising cellulose fibers, for example pulp fibers.
  • the fibrous structures of the present invention that comprise a plurality of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments in an exterior layer, such as a scrim, provides an improved adsorbency, without a gooey feel, than known fibrous structures, such that the hydroxyl polymer fibrous elements during use contact the user's skin surface and trap and/or lock in the bowel movement or portions thereof.
  • the fibrous structures of the present invention that comprise a plurality of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments in an exterior layer, such as a scrim, that provide improved surface properties permits a user to apply more force to the fibrous structure during use because the hydroxyl polymer fibrous elements provide a cushion and/or buffer compared to known fibrous structures, especially known wet-laid and/or air-laid fibrous structures that consist or consist essentially of pulp fibers.
  • the fibrous structures of the present invention may also exhibit a novel glide value, that permits a more comfortable wiping experience when a user uses the fibrous structure to remove bowel movement and/or urine from the user's body, for example skin.
  • the fibrous structures of the present invention may be embossed and/or tufted that creates a three-dimensional surface pattern that provides aesthetics and/or improved cleaning properties.
  • the level of improved cleaning properties relates to the % contact area under a load, such as a user's force applied to the fibrous structure during wiping, and/or % volume/area under a load, such as a user's force applied to the fibrous structure during wiping, created by the three-dimensional surface pattern on the surface of the fibrous structure.
  • the emboss area may be greater than 10% and/or greater than 12% and/or greater than 15% and/or greater than 20% of the surface area of at least one surface of the fibrous structure. Even with such a high emboss area, the fibrous structures of the present invention still exhibit the improved surface properties, for example as measured according to the Emtec Test Method, as described above.
  • the fibrous structure of the present invention may comprise two or more layers, for example a first layer comprising a plurality of first fibrous elements and a second layer comprising a plurality of second fibrous elements, wherein the first and second layers exhibit different common intensive property values for at least one common intensive property, for example bulk, density, opacity, absorbency, strength, and/or softness.
  • the first layer and second layer may exhibit different bulk common intensive properties, for example different bulk densities.
  • the fibrous structure of the present invention is a layered fibrous structure, for example a layered, dispersible fibrous structure comprising a first layer comprising a plurality of fibrous elements that exhibit a smooth exterior surface and a second layer comprising a first web material comprising a plurality of fibrous elements that exhibit a rough exterior surface compared to the fibrous elements of the first layer.
  • a surface of the surface material may be a consumer-contacting surface such that during use of the fibrous structure the consumer wipes the surface of the surface material, such as the second web material, across the skin of the consumer or another person, such as the consumer's child.
  • the surface material for example second web material, may be associated with the first web material by bonding, such as thermal bond sites and/or adhesive bond sites.
  • a multi-ply fibrous structure may comprise a first fibrous structure ply and a second fibrous structure ply wherein at least one of the first and second fibrous structure plies is a fibrous structure according to the present invention.
  • both the first and second fibrous structure plies are fibrous structures according to the present invention.
  • the first and second fibrous structure plies may be associated with one another by bonding, such as thermal bond sites and/or adhesive bond sites.
  • the first and second fibrous structure plies are associated with one another such that the surface material of both the first and second fibrous structure plies form exterior surfaces of the multi-ply fibrous structure and the first web material of both the first and second fibrous structure plies form inner web materials within the multi-ply fibrous structure.
  • the multi-ply fibrous structure according to the present invention may comprise a first fibrous structure ply and a second fibrous structure ply, which may be glued together by adhesive bond sites to form the multi-ply fibrous structure.
  • the first fibrous structure ply comprises an exterior layer, the surface material, for example the second web material, comprising a plurality of fibrous elements, for example a plurality of filaments, such as hydroxyl polymer filaments, for example starch and/or starch derivative filaments, present at a level of greater than 6 and/or greater than 8 and/or greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or at least 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm, an additional layer, the first web material comprises a plurality of fibrous elements, for example a plurality of fibers, such as pulp fibers, for example wood pulp fibers, present at a level of greater than 6 and/or
  • the fibrous structure comprises one or more voids (vacuoles) defined by two different materials, for example both the surface material and the first web material.
  • a void may be formed by the surface material bridging a texture, such as a depression or channel, such as imparted to a surface of the first web material by a patterned molding member, for example a patterned resin molding member and/or a through-air-dried fabric, such as a coarse through-air-dried fabric, for example as is used in the UCTAD process, and/or an embossing operation and/or a creping operation, such as a belt creping operation and/or a fabric creping operation and/or creping off a drying cylinder, such as a Yankee.
  • the voids of the fibrous structures may be seen using different imaging tools, such as ⁇ CT.
  • the fibrous structure of the present invention may comprise a monoplanar material, for example the surface material, and a multi-planar material, for example the first web material that comprises a texture.
  • the surface material may comprise a water soluble polymer, such as a non-crystalline polymer, for example starch and/or starch derivative and/or polyvinylalcohol
  • the first web material may comprise a water insoluble polymer, such as a crystalline polymer, for example cellulose.
  • the surface material may comprise a crosslinked polymer, for example crosslinked starch and/or starch derivative and/or crosslinked polyvinyl alcohol, crosslinked by a first crosslinking agent, such as dihydroxyethyleneurea, and the first web material may comprise a second crosslinking agent different from the first crosslinking agent, such as a crosslinking agent that crosslink its fibrous elements together, such as temporary wet strength crosslinking agent utilized in toilet tissue, for example polyamide-epichlorohydrin chemistries.
  • a crosslinked polymer for example crosslinked starch and/or starch derivative and/or crosslinked polyvinyl alcohol
  • a first crosslinking agent such as dihydroxyethyleneurea
  • the first web material may comprise a second crosslinking agent different from the first crosslinking agent, such as a crosslinking agent that crosslink its fibrous elements together, such as temporary wet strength crosslinking agent utilized in toilet tissue, for example polyamide-epichlorohydrin chemistries.
  • the surface material for example the second web material may comprise a plurality of fibrous elements, for example a plurality of smooth fibrous elements, such as smooth spun filaments, in other words, the exterior surface of the fibrous elements is non-textured, at least relative to the fibrous elements of the first web material, for example pulp fibers, such as wood pulp fibers, which are textured relative to the smooth fibrous elements of the second web material.
  • the surface material for example the second web material may comprise a plurality of fibrous elements, for example filaments, that exhibit an average diameter (less than 10 ⁇ m) less than the average diameter (greater than 10 ⁇ m and/or greater than 12 ⁇ m) of the fibrous elements, for example fibers, such as pulp fibers, of the first web material.
  • the surface material for example the second web material may comprise a plurality of fibrous elements, for example filaments, that exhibit a length (greater than 5.08 cm) greater than the length (5.08 cm or less) of the fibrous elements, for example fibers, such as pulp fibers, of the first web material.
  • the fibrous structure of the present invention may further comprise a second surface material to mitigate and/or prevent pilling of the surface material, for example the second web material, during use by a consumer.
  • the second surface material comprises a third web material comprising a plurality of fibrous elements, for example a plurality of filaments.
  • the third web material may be the same or different from the first surface material, for example the second web material.
  • the second surface material, for example third web material is present at a weight level of less than the first surface material, for example second web material.
  • the third web material may be present at a basis weight of from about 0.25 gsm to about 5 gsm and/or from about 0.5 gsm to about 4 gsm and/or from about 1 gsm to about 3 gsm and the second web material may be present at a basis weight of greater than 6 gsm and/or greater than 8 gsm and/or greater than 9 gsm and/or greater than 10 gsm and/or from about 10 gsm to about 40 gsm and/or to about 25 gsm.
  • the second surface material, for example third web material comprises a hydroxyl polymer different from the first surface material, for example second web material.
  • the second surface material, for example third web material may comprise polyvinyl alcohol and the first surface material, for example second web material may comprise starch and/or a starch derivative.
  • the fibrous structure of the present invention may be made by the fibrous structure making process by providing a first web material comprising a plurality of fibrous elements, for example fibers, and depositing a surface material, for example a plurality of fibrous elements, for example filaments, from one or more surface material sources, such as a die, for example a meltblow die, such as a multi-row capillary die, in this case to form a second web material of inter-entangled fibrous elements, for example filaments, onto at least one surface of the first web material to form the fibrous structure of the present invention.
  • a first web material comprising a plurality of fibrous elements, for example fibers
  • a surface material for example a plurality of fibrous elements, for example filaments
  • the fibrous structure making process may further comprise the step of associating the surface material to the first web material such as by bonding, for example creating thermal bond sites by passing the surface material riding on the first web material through a nip formed a patterned thermal bond roll and a flat roll.
  • the fibrous structure making process may optionally comprise the step of winding the fibrous structure into a roll, such as a parent roll for unwinding in a converting operation to cut the roll into consumer-useable sized sanitary tissue product rolls and/or emboss the fibrous structure and/or perforate the fibrous structure into consumer-useable sized sheets of sanitary tissue product.
  • the roll of fibrous structure may be combined with another fibrous structure ply, the same or different as the roll of fibrous structure to make a multi-ply fibrous structure according to the present invention.
  • the multi-row capillary die (surface material source) comprises at least one fibrous element-forming hole, and/or 2 or more and/or 3 or more rows of fibrous element-forming holes from which filaments are spun. At least one row of the fibrous element-forming holes contains 2 or more and/or 3 or more and/or 10 or more fibrous element-forming holes.
  • the multi-row capillary die comprises fluid-releasing holes, such as gas-releasing holes, in one example air-releasing holes, that provide attenuation to the filaments formed from the fibrous element-forming holes.
  • One or more fluid-releasing holes may be associated with a fibrous element-forming hole such that the fluid exiting the fluid-releasing hole is parallel or substantially parallel (rather than angled like a knife-edge die) to an exterior surface of a filament exiting the fibrous element-forming hole.
  • the fluid exiting the fluid-releasing hole contacts the exterior surface of a filament formed from a fibrous element-forming hole at an angle of less than 30° and/or less than 20° and/or less than 10° and/or less than 5° and/or about 0°.
  • One or more fluid releasing holes may be arranged around a fibrous element-forming hole.
  • one or more fluid-releasing holes are associated with a single fibrous element-forming hole such that the fluid exiting the one or more fluid releasing holes contacts the exterior surface of a single filament formed from the single fibrous element-forming hole.
  • the fluid-releasing hole permits a fluid, such as a gas, for example air, to contact the exterior surface of a filament formed from a fibrous element-forming hole rather than contacting an inner surface of a filament, such as what happens when a hollow filament is formed.
  • one or more plies of the fibrous structure according to the present invention may be combined, for example with glue, with another ply of fibrous structure, which may also be a fibrous structure according to the present invention, to form a multi-ply sanitary tissue product.
  • the multi-ply sanitary tissue product may be formed by combining two or more plies of fibrous structure according to the present invention.
  • the fibrous structures of the present invention may be non-lotioned and/or may not contain a post-applied surface chemistry.
  • the fibrous structures of the present invention may be creped or uncreped.
  • the fibrous structures of the present invention are uncreped fibrous structures.
  • such fibrous structures may exhibit improved cleaning properties, for example bowel movement cleaning properties, compared to known fibrous structures, for example known fibrous structures comprising hydroxyl polymer filaments and known fibrous structures, such as wet-laid and/or air-laid, comprising cellulose fibers, for example pulp fibers.
  • the fibrous structures of the present invention exhibit improved skin benefit and/or glide on skin properties and/or cleaning properties due to the hydroxyl polymer fibrous elements of the present invention exhibiting greater absorbency, without a gooey feel, than pulp fibers, and therefore facilitates better, in reality and/or perception, absorption of bowel movement and/or urine more completely and/or faster than known fibrous structures.
  • the fibrous structures of the present invention that comprise a plurality of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments in an exterior layer, such as a scrim, provides an improved adsorbency, without a gooey feel, than known fibrous structures, such that the hydroxyl polymer fibrous elements during use contact the user's skin surface and trap and/or lock in the bowel movement or portions thereof.
  • the fibrous structures of the present invention that comprise a plurality of hydroxyl polymer fibrous elements, for example hydroxyl polymer filaments in an exterior layer that provide improved surface properties permits a user to apply more force to the fibrous structure during use because the hydroxyl polymer fibrous elements provide a cushion and/or buffer compared to known fibrous structures, especially known wet-laid and/or air-laid fibrous structures that consist or consist essentially of pulp fibers.
  • the fibrous structures of the present invention may be embossed and/or tufted that creates a three-dimensional surface pattern that provides aesthetics and/or improved cleaning properties.
  • the level of improved cleaning properties relates to the % contact area under a load, such as a user's force applied to the fibrous structure during wiping, and/or % volume/area under a load, such as a user's force applied to the fibrous structure during wiping, created by the three-dimensional surface pattern on the surface of the fibrous structure.
  • the emboss area may be greater than 10% and/or greater than 12% and/or greater than 15% and/or greater than 20% of the surface area of at least one surface of the fibrous structure.
  • the fibrous structure of the present invention may comprise two or more components, for example a first component comprising a first web material that exhibits a different bulk density from the second component, such as a surface material.
  • the fibrous structure comprises a least one surface, a consumer-contacting surface, that comes into contact with a consumer during use, such as during wiping.
  • the surface of the fibrous structure may comprise and/or be defined by at least a portion of the first web material.
  • the first web material comprises a plurality of fibrous elements, for example a plurality of fibers.
  • the first web material comprises a plurality of naturally-occurring fibers, for example pulp fibers, such as wood pulp fibers (hardwood and/or softwood pulp fibers).
  • the first web material comprises a plurality of non-naturally occurring fibers (synthetic fibers), for example staple fibers, such as rayon, lyocell, polyester fibers, polycaprolactone fibers, polylactic acid fibers, polyhydroxyalkanoate fibers, and mixtures thereof.
  • the first web material may comprise one or more filaments, such as polyolefin filaments, for example polypropylene and/or polyethylene filaments, starch filaments, starch derivative filaments, cellulose filaments, polyvinyl alcohol filaments.
  • polyolefin filaments for example polypropylene and/or polyethylene filaments
  • starch filaments for example starch filaments, starch derivative filaments
  • cellulose filaments for example polyvinyl alcohol filaments.
  • the first web material of the present invention may be single-ply or multi-ply web material.
  • the first web materials of the present invention may comprise one or more first web materials, the same or different from each other so long as one of them comprises a plurality of pulp fibers.
  • the first web material comprises a wet laid fibrous structure ply, such as a through-air-dried fibrous structure ply, for example an uncreped, through-air-dried fibrous structure ply and/or a creped, through-air-dried fibrous structure ply.
  • the first web material and/or wet laid fibrous structure ply may exhibit substantially uniform density.
  • the first web material and/or wet laid fibrous structure ply may comprise a surface pattern.
  • the wet laid fibrous structure ply comprises a conventional wet-pressed fibrous structure ply.
  • the wet laid fibrous structure ply may comprise a fabric-creped fibrous structure ply.
  • the wet laid fibrous structure ply may comprise a belt-creped fibrous structure ply.
  • the first web material may comprise an air laid fibrous structure ply.
  • the first web materials of the present invention may comprise a surface softening agent or be void of a surface softening agent, such as silicones, quaternary ammonium compounds, lotions, and mixtures thereof.
  • a surface softening agent such as silicones, quaternary ammonium compounds, lotions, and mixtures thereof.
  • the sanitary tissue product is a non-lotioned first web material.
  • the first web materials of the present invention may comprise trichome fibers or may be void of trichome fibers.
  • the first web materials of the present invention may be formed on patterned molding members that result in the first web materials of the present invention.
  • the pattern molding member comprises a non-random repeating pattern.
  • the pattern molding member comprises a resinous pattern.
  • the first web material comprises a textured surface.
  • the first web material comprises a surface comprising a three-dimensional (3D) pattern, for example a 3D pattern imparted to the first web material by a patterned molding member.
  • suitable patterned molding members include patterned felts, patterned forming wires, patterned rolls, patterned fabrics, and patterned belts utilized in conventional wet-pressed papermaking processes, air-laid papermaking processes, and/or wet-laid papermaking processes that produce 3D patterned sanitary tissue products and/or 3D patterned fibrous structure plies employed in sanitary tissue products.
  • patterned molding members include through-air-drying fabrics and through-air-drying belts utilized in through-air-drying papermaking processes that produce through-air-dried fibrous structures, for example 3D patterned through-air dried fibrous structures, and/or through-air-dried sanitary tissue products comprising the first web material.
  • the first web material comprises a 3D patterned first web material having a surface comprising a 3D pattern comprising a first series of line elements that are oriented at an angle of between ⁇ 20° to 20° with respect the 3D patterned first web material's machine direction.
  • the first web material may be made by any suitable method, such as wet-laid, air laid, coform, hydroentangling, carding, meltblowing, spunbonding, and mixtures thereof.
  • the method for making the first web material of the present invention comprises the step of depositing a plurality of fibers onto a collection device, such as a 3D patterned molding member, such as a molding member comprising a first series of line elements that are oriented at an angle of between ⁇ 40° to 40° and/or ⁇ 30° to 30° and/or ⁇ 20° to 20° with respect the 3D patterned first web material's machine direction such that a first web material is formed.
  • a “reinforcing element” may be a desirable (but not necessary) element in some examples of the molding member, serving primarily to provide or facilitate integrity, stability, and durability of the molding member comprising, for example, a resinous material.
  • the reinforcing element can be fluid-permeable or partially fluid-permeable, may have a variety of embodiments and weave patterns, and may comprise a variety of materials, such as, for example, a plurality of interwoven yarns (including Jacquard-type and the like woven patterns), a felt, a plastic, other suitable synthetic material, or any combination thereof.
  • a non-limiting example of a patterned molding member suitable for use in the present invention comprises a through-air-drying belt.
  • the through-air-drying belt comprises a plurality of semi-continuous knuckles formed by semi-continuous line segments of resin arranged in a non-random, repeating pattern, for example a substantially machine direction repeating pattern of semi-continuous line segments supported on a support fabric comprising filaments.
  • the semi-continuous line segments are curvilinear, for example sinusoidal.
  • the semi-continuous knuckles are spaced from adjacent semi-continuous knuckles by semi-continuous pillows, which constitute deflection conduits into which portions of a fibrous structure ply being made on the through-air-drying belt.
  • a resulting first web material being made on the through-air-drying belt comprises semi-continuous pillow regions imparted by the semi-continuous pillows of the through-air-drying belt.
  • the sanitary tissue product further comprises semi-continuous knuckle regions imparted by the semi-continuous knuckles of the through-air-drying belt.
  • the semi-continuous pillow regions and semi-continuous knuckle regions may exhibit different densities, for example, one or more of the semi-continuous knuckle regions may exhibit a density that is greater than the density of one or more of the semi-continuous pillow regions.
  • the first web materials of the present invention may be made by any suitable papermaking process, such as conventional wet press papermaking process, through-air-dried papermaking process, belt-creped papermaking process, fabric-creped papermaking process, creped papermaking process, uncreped papermaking process, coform process, and air-laid process, so long as the first web material comprises a plurality of fibers.
  • the first web material is made on a molding member of the present invention is used to make the first web material of the present invention.
  • the method may be a first web material making process that uses a cylindrical dryer such as a Yankee (a Yankee-process) or it may be a Yankeeless process as is used to make substantially uniform density and/or uncreped first web materials (fibrous structures).
  • the first web materials may be made by an air-laid process and/or meltblown and/or spunbond processes and any combinations thereof so long as the first web materials of the present invention are made thereby.
  • One example of a process and equipment for making a first web material according to the present invention comprises supplying an aqueous dispersion of fibers (a fibrous furnish or fiber slurry) to a headbox which can be of any convenient design. From headbox the aqueous dispersion of fibers is delivered to a first foraminous member which is typically a Fourdrinier wire, to produce an embryonic fibrous structure.
  • a first foraminous member typically a Fourdrinier wire
  • the first foraminous member may be supported by a breast roll and a plurality of return rolls.
  • the first foraminous member can be propelled in the direction indicated by directional arrow by a drive means.
  • Optional auxiliary units and/or devices commonly associated fibrous structure making machines and with the first foraminous member include forming boards, hydrofoils, vacuum boxes, tension rolls, support rolls, wire cleaning showers, and the like.
  • embryonic fibrous structure is formed, typically by the removal of a portion of the aqueous dispersing medium by techniques well known to those skilled in the art. Vacuum boxes, forming boards, hydrofoils, and the like are useful in effecting water removal.
  • the embryonic web material may travel with the first foraminous member about return roll and is brought into contact with a patterned molding member, such as a 3D patterned through-air-drying belt. While in contact with the patterned molding member, the embryonic web material will be deflected, rearranged, and/or further dewatered. This can be accomplished by applying differential speeds and/or pressures.
  • the patterned molding member may be in the form of an endless belt.
  • the patterned molding member passes around and about patterned molding member return rolls and impression nip roll and may travel in the direction indicated by directional arrow.
  • Associated with patterned molding member may be various support rolls, other return rolls, cleaning means, drive means, and the like well known to those skilled in the art that may be commonly used in fibrous structure making machines.
  • the embryonic web material can be referred to as an intermediate web material.
  • sufficient water may be removed, such as by a noncompressive process, from the embryonic web material before it becomes associated with the patterned molding member so that the consistency of the embryonic web material may be from about 10% to about 30%.
  • water removal occurs both during and after deflection; this water removal may result in a decrease in fiber mobility in the embryonic web material. This decrease in fiber mobility may tend to fix and/or freeze the fibers in place after they have been deflected and rearranged. Of course, the drying of the web material in a later step in the process of this invention serves to more firmly fix and/or freeze the fibers in position.
  • Any convenient means conventionally known in the papermaking art can be used to dry the intermediate web material. Examples of such suitable drying process include subjecting the intermediate web material to conventional and/or flow-through dryers and/or Yankee dryers.
  • the intermediate web material in association with the patterned molding member passes around the patterned molding member return roll and travels in the direction indicated by directional arrow.
  • the intermediate web material may first pass through an optional predryer.
  • This predryer can be a conventional flow-through dryer (hot air dryer) well known to those skilled in the art.
  • the predryer can be a so-called capillary dewatering apparatus. In such an apparatus, the intermediate web material passes over a sector of a cylinder having preferential-capillary-size pores through its cylindrical-shaped porous cover.
  • the predryer can be a combination capillary dewatering apparatus and flow-through dryer.
  • the quantity of water removed in the predryer may be controlled so that a predried web material exiting the predryer has a consistency of from about 30% to about 98%.
  • the predried web material which may still be associated with patterned molding member, may pass around another patterned molding member return roll and as it travels to an impression nip roll.
  • the pattern formed by the top surface of patterned molding member is impressed into the predried web material to form a 3D patterned web material, a first web material of the present invention.
  • the 3D patterned web material can then be adhered to the surface of the Yankee dryer 94 where it can be dried to a consistency of at least about 95%.
  • the 3D patterned web material can then be foreshortened by creping the 3D patterned web material with a creping blade to remove the 3D patterned web material from the surface of the Yankee dryer resulting in the production of a 3D patterned creped web material, a first web material in accordance with the present invention.
  • foreshortening refers to the reduction in length of a dry (having a consistency of at least about 90% and/or at least about 95%) web material which occurs when energy is applied to the dry web material in such a way that the length of the dry web material is reduced and the fibers in the dry web material are rearranged with an accompanying disruption of fiber-fiber bonds.
  • Foreshortening can be accomplished in any of several well-known ways. One common method of foreshortening is creeping.
  • the 3D patterned creped web material may be subjected to post processing steps such as calendaring, tuft generating operations, and/or embossing and/or converting.
  • the fibrous structure of the present invention comprises a surface material.
  • the surface material of the fibrous structure is different from the first web material.
  • the surface material may be associated with the first web material, directly (meaning in direct contact with a surface of the first web material) and/or indirectly (meaning one or more intermediate materials are positioned between the surface of the first web material and the surface material.
  • the surface material is associated with the first web material through one or more bond sites, for example at least one of the bond sites comprise a thermal bond and/or at least one of the bond sites comprises an adhesive bond.
  • the surface material may be directly bonded to a surface of the first web material.
  • the surface material may be indirectly bonded to a surface of the first web material by being bonded to one or more intermediate materials positioned between the surface of the first web material and the surface material.
  • the intermediate materials may be fibrous elements, web materials, liquids, particles, and/or surface coatings, such as surface softening agents, present on the surface of the first web material.
  • the surface material comprises a second web material.
  • the second web material may comprise a plurality of fibrous elements, such as fibers and/or filaments.
  • the second web material comprise a plurality of naturally-occurring fibers, for example pulp fibers, such as wood pulp fibers (hardwood and/or softwood pulp fibers).
  • the second web material comprises a plurality of non-naturally occurring fibers (synthetic fibers), for example staple fibers, such as rayon, lyocell, polyester fibers, polycaprolactone fibers, polylactic acid fibers, polyhydroxyalkanoate fibers, hydroxyl polymer fibers, such as polyvinyl alcohol fibers and/or polysaccharide fibers, for example cellulose, cellulose derivatives, starch, starch derivatives, hemicelluloses, hemicelluloses derivatives, and mixtures thereof.
  • staple fibers such as rayon, lyocell, polyester fibers, polycaprolactone fibers, polylactic acid fibers, polyhydroxyalkanoate fibers, hydroxyl polymer fibers, such as polyvinyl alcohol fibers and/or polysaccharide fibers, for example cellulose, cellulose derivatives, starch, starch derivatives, hemicelluloses, hemicelluloses derivatives, and mixtures thereof.
  • staple fibers such as rayon, lyocell, polyester fiber
  • the second web material may comprise one or more filaments, for example one or more filaments comprising a polymer, such as polyolefin filaments, for example polypropylene filaments and/or polyethylene filaments, and/or a hydroxyl polymer filament, such as cellulose filaments, cellulose derivative filaments, starch filaments, starch derivative filaments, hemicelluloses filaments, hemicelluloses derivative filaments, and mixtures thereof.
  • a polymer such as polyolefin filaments, for example polypropylene filaments and/or polyethylene filaments
  • a hydroxyl polymer filament such as cellulose filaments, cellulose derivative filaments, starch filaments, starch derivative filaments, hemicelluloses filaments, hemicelluloses derivative filaments, and mixtures thereof.
  • the filaments of the second web material may exhibit an average diameter of less than 50 ⁇ m and/or less than 25 ⁇ m and/or less than 20 ⁇ m and/or less than 15 ⁇ m and/or less than 10 ⁇ m and/or greater than 1 ⁇ m and/or greater than 3 ⁇ m and/or from about 3-10 ⁇ m and/or from about 3-8 ⁇ m and/or from about 5-7 ⁇ m as measured according to the Average Diameter Test Method described herein.
  • the filaments of the second web material comprise a crosslinked polymer, such as a crosslinked polyvinyl alcohol and/or a crosslinked starch.
  • the second web material may be a first web material described above so long as the second web material is different from the first web material.
  • the second web material comprises a plurality of fibrous elements that are different from the fibers of the first web material.
  • the second web material exhibits a basis weight that is different from the basis weight of the first web material as measured according to the Basis Weight Test Method described herein.
  • the surface material comprises a second web material comprising a plurality of filaments, for example a plurality of hydroxyl polymer filaments such as hydroxyl polymer filaments comprising a polymer selected from the group consisting of: polyvinyl alcohol, starch, starch derivatives, and mixtures thereof.
  • One solution to the problem identified above is to make fibrous structures comprising a plurality of hydroxyl polymer filaments present in at least one exterior layer of the fibrous structure at greater than 10 gsm such that the fibrous structure exhibits average Emtec values as measured according to the Emtec Test Method described herein that are less than the average Emtec values exhibited by known fibrous structures comprising lower levels (2 to 3 gsm for example) of hydroxyl polymer filaments in their exterior layers.
  • the improved ability to increase the level of hydroxyl polymer filaments in the exterior layers of the fibrous structures of the present invention is attributable to features of the polymer melt composition as described herein, for example the type of hydroxyl polymer and/or the effectiveness of the crosslinking of the hydroxyl polymer, which relates at least partially to the level of base such as triethanolamine present in the crosslinking agent used to make the hydroxyl polymer fibrous elements, for example less than 2% and/or less than 1.8% and/or less than 1.5% and/or less than 1.25% and/or about 0% and/or about 0.25% and/or about 0.5% by weight, to produce the hydroxyl polymer fibrous elements.
  • the level of base such as triethanolamine present in the crosslinking agent used to make the hydroxyl polymer fibrous elements
  • a fibrous structure comprising a plurality of hydroxyl polymer filaments present in at least one exterior layer of the fibrous structure at a level of greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or at least 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm is provided.
  • the second web material may comprise a plurality of hydroxyl polymer fibrous elements at a basis weight of greater than 6 and/or greater than 8 and/or greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or greater than 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 g/m 2 (“gsm”) and/or from about 12 to about 40 g/m 2 and/or from about 12 to about 35 g/m 2 and/or from about 12 to about 30 g/m 2 and/or from about 16 to about 25 g/m 2 .
  • the basis weight of the scrim material and/or exterior layer or other layers of the fibrous structure are known by the manufacturer when making the fibrous structure and may be determined by other means such as tape stripping or other suitable means known to those in the art.
  • a fibrous structure comprising a first outer layer comprising a plurality of hydroxyl polymer filaments present in the first outer layer at a basis weight of greater than 10 gsm.
  • An example of a method for making a surface material, for example a second web material, according to the present invention comprises the step of spinning a polymer melt composition comprising a polymer, for example a hydroxyl polymer, a crosslinking agent, and optionally, a surfactant, into a plurality of fibrous elements, for example a plurality of hydroxyl polymer filaments.
  • the plurality of fibrous elements may be spun directly onto the first web material and/or collected on a collection device and then subsequently associated with the first web material.
  • the plurality of fibrous elements for example the plurality of hydroxyl polymer filaments may be present as the exterior layer of the fibrous structure of the present invention at a level of greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or at least 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 gsm.
  • the present invention provides novel fibrous structures that comprise a higher level of hydroxyl polymer filaments in at least one exterior layer of the fibrous structure compared to known fibrous structures comprising hydroxyl polymer filaments in their exterior layers, and methods for making such fibrous structures.
  • the fibrous elements of the present invention may be produced from a polymer melt composition, for example a hydroxyl polymer melt composition such as an aqueous hydroxyl polymer melt composition, comprising a hydroxyl polymer, such as an uncrosslinked starch for example a dent corn starch, an acid-thinned starch, and/or a starch derivative such as an ethoxylated starch, a crosslinking system comprising a crosslinking agent, such as an imidazolidinone, and water.
  • a hydroxyl polymer melt composition such as an aqueous hydroxyl polymer melt composition
  • a hydroxyl polymer such as an uncrosslinked starch for example a dent corn starch, an acid-thinned starch, and/or a starch derivative such as an ethoxylated starch
  • a crosslinking system comprising a crosslinking agent, such as an imidazolidinone, and water.
  • the crosslinking agent comprises less than 2% and/or less than 1.8% and/or less than 1.5% and/or less than 1.25% and/or 0% and/or about 0.25% and/or about 0.50% by weight of a base, for example triethanolamine. It has unexpectedly been found that the reducing the level of base in the crosslinking agent used in the polymer melt composition results in more effective crosslinking.
  • the fibrous elements of the present invention comprise greater than 25% and/or greater than 40% and/or greater than 50% and/or greater than 60% and/or greater than 70% to about 95% and/or to about 90% and/or to about 80% by weight of the fibrous element of a hydroxyl polymer, such as starch, which may be in a crosslinked state.
  • the fibrous element comprises an ethoxylated starch and an acid thinned starch, which may be in their crosslinked states.
  • the fibrous elements may also comprise a crosslinking agent, such as an imidazolidinone, which may be in its crosslinked state (crosslinking the hydroxyl polymers present in the fibrous elements) at a level of from about 0.25% and/or from about 0.5% and/or from about 1% and/or from about 2% and/or from about 3% and/or to about 10% and/or to about 7% and/or to about 5.5% and/or to about 4.5% by weight of the fibrous element.
  • a crosslinking agent such as an imidazolidinone
  • the fibrous element may comprise a crosslinking facilitator that aids the crosslinking agent at a level of from 0% and/or from about 0.3% and/or from about 0.5% and/or to about 2% and/or to about 1.7% and/or to about 1.5% by weight of the fibrous element.
  • the hydroxyl polymer fibrous element for example hydroxyl polymer filament, comprises a crosslinked hydroxyl polymer, such as a crosslinked starch and/or starch derivative.
  • the polymer melt composition may also comprise a surfactant, such as a sulfosuccinate surfactant.
  • a surfactant such as a sulfosuccinate surfactant.
  • a non-limiting example of a suitable sulfosuccinate surfactant comprises Aerosol® AOT (a sodium dioctyl sulfosuccinate) and/or Aerosol® MA-80 (a sodium dihexyl sulfosuccinate), which are commercially available from Cytec.
  • the surfactant, such as a sulfosuccinate surfactant may be present at a level of from 0% and/or from about 0.1% and/or from about 0.3% to about 2% and/or to about 1.5% and/or to about 1.1% and/or to about 0.7% by weight of the fibrous element.
  • the polymer melt composition may comprise a crosslinking facilitator such as ammonium salts of methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, isopropylsulfonic acid, butanesulfonic acid, isobutylsulfonic acid, sec-butylsulfonic acids, benzenesulfonic acid, toluenesulfonic acid, xylenesulfonic acid, cumenesulfonic acid, alkylbenzenesulfonic, alkylnaphthalenedisulfonic acids.
  • a crosslinking facilitator such as ammonium salts of methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, isopropylsulfonic acid, butanesulfonic acid, isobutylsulfonic acid, sec-butylsulfonic acids, benzenesulfonic acid, toluenesulfonic
  • the fibrous elements may also comprise a polymer selected from the group consisting of: polyacrylamide and its derivatives; acrylamide-based copolymers, polyacrylic acid, polymethacrylic acid, and their esters; polyethyleneimine; copolymers made from mixtures of monomers of the aforementioned polymers; and mixtures thereof at a level of from 0% and/or from about 0.01% and/or from about 0.05% and/or to about 0.5% and/or to about 0.3% and/or to about 0.2% by weight of the fibrous element.
  • Such polymers may exhibits a weight average molecular weight of greater than 500,000 g/mol.
  • the fibrous element comprises polyacrylamide.
  • the fibrous elements may also comprise various other ingredients such as propylene glycol, sorbitol, glycerin, and mixtures thereof.
  • One or more hueing agents such as Violet CT may also be present in the polymer melt composition and/or fibrous elements formed therefrom.
  • the fibrous elements, of the present invention comprise a fibrous element-forming polymer, such as a hydroxyl polymer, for example a crosslinked hydroxyl polymer.
  • the fibrous elements may comprise two or more fibrous element-forming polymers, such as two or more hydroxyl polymers.
  • the fibrous element may comprise two or more fibrous element-forming polymers, such as two or more hydroxyl polymers, at least one of which is starch and/or a starch derivative.
  • the fibrous elements of the present invention may comprise two or more fibrous element-forming polymers at least one of which is a hydroxyl polymer and at least one of which is a non-hydroxyl polymer.
  • the fibrous elements of the present invention may comprise two or more non-hydroxyl polymers.
  • at least one of the non-hydroxyl polymers exhibits a weight average molecular weight of greater than 1,400,000 g/mol and/or is present in the fibrous elements at a concentration greater than its entanglement concentration (C e ) and/or exhibits a polydispersity of greater than 1.32.
  • at least one of the non-hydroxyl polymers comprises an acrylamide-based copolymer.
  • the fibrous element comprises a filament.
  • the fibrous element comprises a fiber, such as a filament that has been cut into fibers.
  • Table 1 below shows Average TS7 Values and/or Average TS750 Values as measured according to the Emtec Test Method described herein of representative samples of uncreped prior art fibrous structures, both filament-containing, and non-filament containing, and inventive examples according to the present invention.
  • the fibrous elements of the present invention may be produced from a polymer melt composition, for example a hydroxyl polymer melt composition such as an aqueous hydroxyl polymer melt composition, comprising a hydroxyl polymer, such as an uncrosslinked starch for example a dent corn starch, an acid-thinned starch, and/or a starch derivative such as an ethoxylated starch, a crosslinking system comprising a crosslinking agent, such as an imidazolidinone, and water.
  • a hydroxyl polymer melt composition such as an aqueous hydroxyl polymer melt composition
  • a hydroxyl polymer such as an uncrosslinked starch for example a dent corn starch, an acid-thinned starch, and/or a starch derivative such as an ethoxylated starch
  • a crosslinking system comprising a crosslinking agent, such as an imidazolidinone, and water.
  • the crosslinking agent comprises less than 2% and/or less than 1.8% and/or less than 1.5% and/or less than 1.25% and/or 0% and/or about 0.25% and/or about 0.50% by weight of a base, for example triethanolamine. It has unexpectedly been found that the reducing the level of base in the crosslinking agent used in the polymer melt composition results in more effective crosslinking.
  • the fibrous elements of the present invention comprise greater than 25% and/or greater than 40% and/or greater than 50% and/or greater than 60% and/or greater than 70% to about 95% and/or to about 90% and/or to about 80% by weight of the fibrous element of a hydroxyl polymer, such as starch, which may be in a crosslinked state.
  • the fibrous element comprises an ethoxylated starch and an acid thinned starch, which may be in their crosslinked states.
  • the fibrous elements may also comprise a crosslinking agent, such as an imidazolidinone, which may be in its crosslinked state (crosslinking the hydroxyl polymers present in the fibrous elements) at a level of from about 0.25% and/or from about 0.5% and/or from about 1% and/or from about 2% and/or from about 3% and/or to about 10% and/or to about 7% and/or to about 5.5% and/or to about 4.5% by weight of the fibrous element.
  • a crosslinking agent such as an imidazolidinone
  • the fibrous element may comprise a crosslinking facilitator that aids the crosslinking agent at a level of from 0% and/or from about 0.3% and/or from about 0.5% and/or to about 2% and/or to about 1.7% and/or to about 1.5% by weight of the fibrous element.
  • the hydroxyl polymer fibrous element for example hydroxyl polymer filament, comprises a crosslinked hydroxyl polymer, such as a crosslinked starch and/or starch derivative.
  • the polymer melt composition may also comprise a surfactant, such as a sulfosuccinate surfactant.
  • a surfactant such as a sulfosuccinate surfactant.
  • a non-limiting example of a suitable sulfosuccinate surfactant comprises Aerosol® AOT (a sodium dioctyl sulfosuccinate) and/or Aerosol® MA-80 (a sodium dihexyl sulfosuccinate), which are commercially available from Cytec.
  • the surfactant, such as a sulfosuccinate surfactant may be present at a level of from 0% and/or from about 0.1% and/or from about 0.3% to about 2% and/or to about 1.5% and/or to about 1.1% and/or to about 0.7% by weight of the fibrous element.
  • the polymer melt composition may comprise a crosslinking facilitator such as ammonium salts of methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, isopropylsulfonic acid, butanesulfonic acid, isobutylsulfonic acid, sec-butylsulfonic acids, benzenesulfonic acid, toluenesulfonic acid, xylenesulfonic acid, cumenesulfonic acid, alkylbenzenesulfonic, alkylnaphthalenedisulfonic acids.
  • a crosslinking facilitator such as ammonium salts of methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, isopropylsulfonic acid, butanesulfonic acid, isobutylsulfonic acid, sec-butylsulfonic acids, benzenesulfonic acid, toluenesulfonic
  • the fibrous elements may also comprise a polymer selected from the group consisting of: polyacrylamide and its derivatives; acrylamide-based copolymers, polyacrylic acid, polymethacrylic acid, and their esters; polyethyleneimine; copolymers made from mixtures of monomers of the aforementioned polymers; and mixtures thereof at a level of from 0% and/or from about 0.01% and/or from about 0.05% and/or to about 0.5% and/or to about 0.3% and/or to about 0.2% by weight of the fibrous element.
  • Such polymers may exhibits a weight average molecular weight of greater than 500,000 g/mol.
  • the fibrous element comprises polyacrylamide.
  • the fibrous elements may also comprise various other ingredients such as propylene glycol, sorbitol, glycerin, and mixtures thereof.
  • One or more hueing agents such as Violet CT may also be present in the polymer melt composition and/or fibrous elements formed therefrom.
  • the fibrous elements, of the present invention comprise a fibrous element-forming polymer, such as a hydroxyl polymer, for example a crosslinked hydroxyl polymer.
  • the fibrous elements may comprise two or more fibrous element-forming polymers, such as two or more hydroxyl polymers.
  • the fibrous element may comprise two or more fibrous element-forming polymers, such as two or more hydroxyl polymers, at least one of which is starch and/or a starch derivative.
  • the fibrous elements of the present invention may comprise two or more fibrous element-forming polymers at least one of which is a hydroxyl polymer and at least one of which is a non-hydroxyl polymer.
  • the fibrous elements of the present invention may comprise two or more non-hydroxyl polymers.
  • at least one of the non-hydroxyl polymers exhibits a weight average molecular weight of greater than 1,400,000 g/mol and/or is present in the fibrous elements at a concentration greater than its entanglement concentration (CO and/or exhibits a polydispersity of greater than 1.32.
  • at least one of the non-hydroxyl polymers comprises an acrylamide-based copolymer.
  • the fibrous element comprises a filament.
  • the fibrous element comprises a fiber, such as a filament that has been cut into fibers.
  • the polymer melt compositions of the present invention for example hydroxyl polymer melt compositions such as aqueous hydroxyl polymer melt compositions, and/or fibrous elements, such as filaments and/or fibers, of the present invention that associate to form fibrous structures of the present invention contain at least one fibrous element-forming polymer, such as a hydroxyl polymer, and may contain other types of polymers such as non-hydroxyl polymers that exhibit weight average molecular weights of greater than 500,000 g/mol and mixtures thereof.
  • hydroxyl polymer melt compositions such as aqueous hydroxyl polymer melt compositions
  • fibrous elements such as filaments and/or fibers
  • Non-limiting examples of hydroxyl polymers in accordance with the present invention include polyols, such as polyvinyl alcohol, polyvinyl alcohol derivatives, polyvinyl alcohol copolymers, starch, starch derivatives, starch copolymers, chitosan, chitosan derivatives, chitosan copolymers, cellulose, cellulose derivatives such as cellulose ether and ester derivatives, cellulose copolymers, hemicellulose, hemicellulose derivatives, hemicellulose copolymers, gums, arabinans, galactans, proteins and various other polysaccharides and mixtures thereof.
  • polyols such as polyvinyl alcohol, polyvinyl alcohol derivatives, polyvinyl alcohol copolymers, starch, starch derivatives, starch copolymers, chitosan, chitosan derivatives, chitosan copolymers, cellulose, cellulose derivatives such as cellulose ether and ester derivatives, cellulose copo
  • a hydroxyl polymer of the present invention comprises a polysaccharide.
  • a hydroxyl polymer of the present invention comprises a non-thermoplastic polymer.
  • the hydroxyl polymer may have a weight average molecular weight of from about 10,000 g/mol to about 40,000,000 g/mol and/or greater than 100,000 g/mol and/or greater than 1,000,000 g/mol and/or greater than 3,000,000 g/mol and/or greater than 3,000,000 g/mol to about 40,000,000 g/mol.
  • Higher and lower molecular weight hydroxyl polymers may be used in combination with hydroxyl polymers having a certain desired weight average molecular weight.
  • Polyvinyl alcohols herein can be grafted with other monomers to modify its properties.
  • a wide range of monomers has been successfully grafted to polyvinyl alcohol.
  • Non-limiting examples of such monomers include vinyl acetate, styrene, acrylamide, acrylic acid, 2-hydroxyethyl methacrylate, acrylonitrile, 1,3-butadiene, methyl methacrylate, methacrylic acid, vinylidene chloride, vinyl chloride, vinyl amine and a variety of acrylate esters.
  • Polyvinyl alcohols comprise the various hydrolysis products formed from polyvinyl acetate. In one example the level of hydrolysis of the polyvinyl alcohols is greater than 70% and/or greater than 88% and/or greater than 95% and/or about 99%.
  • Polysaccharides as used herein means natural polysaccharides and polysaccharide derivatives and/or modified polysaccharides. Suitable polysaccharides include, but are not limited to, starches, starch derivatives, starch copolymers, chitosan, chitosan derivatives, chitosan copolymers, cellulose, cellulose derivatives, cellulose copolymers, hemicellulose, hemicellulose derivatives, hemicelluloses copolymers, gums, arabinans, galactans, and mixtures thereof.
  • the polysaccharide may exhibit a weight average molecular weight of from about 10,000 to about 40,000,000 g/mol and/or greater than about 100,000 and/or greater than about 1,000,000 and/or greater than about 3,000,000 and/or greater than about 3,000,000 to about 40,000,000.
  • the polysaccharides of the present invention may comprise non-cellulose and/or non-cellulose derivative and/or non-cellulose copolymer hydroxyl polymers.
  • Non-limiting example of such non-cellulose polysaccharides may be selected from the group consisting of: starches, starch derivatives, starch copolymers, chitosan, chitosan derivatives, chitosan copolymers, hemicellulose, hemicellulose derivatives, hemicelluloses copolymers, and mixtures thereof.
  • the hydroxyl polymer comprises starch, a starch derivative and/or a starch copolymer. In another example, the hydroxyl polymer comprises starch and/or a starch derivative. In yet another example, the hydroxyl polymer comprises starch. In one example, the hydroxyl polymer comprises ethoxylated starch. In another example, the hydroxyl polymer comprises acid-thinned starch. In still another example, the hydroxyl polymer comprises Dent corn starch.
  • a natural starch can be modified chemically or enzymatically, as well known in the art.
  • the natural starch can be acid-thinned, hydroxy-ethylated, hydroxy-propylated, ethersuccinylated or oxidized.
  • the starch comprises a high amylopectin natural starch (a starch that contains greater than 75% and/or greater than 90% and/or greater than 98% and/or about 99% amylopectin).
  • Such high amylopectin natural starches may be derived from agricultural sources, which offer the advantages of being abundant in supply, easily replenishable and relatively inexpensive.
  • Chemical modifications of starch typically include acid or alkaline-catalyzed hydrolysis and chain scission (oxidative and/or enzymatic) to reduce molecular weight and molecular weight distribution.
  • Suitable compounds for chemical modification of starch include organic acids such as citric acid, acetic acid, glycolic acid, and adipic acid; inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, boric acid, and partial salts of polybasic acids, e.g., KH 2 PO 4 , NaHSO 4 ; group Ia or IIa metal hydroxides such as sodium hydroxide, and potassium hydroxide; ammonia; oxidizing agents such as hydrogen peroxide, benzoyl peroxide, ammonium persulfate, potassium permanganate, hypochloric salts, and the like; and mixtures thereof.
  • Modified starch is a starch that has been modified chemically or enzymatically.
  • the modified starch is contrasted with a native starch, which is a starch that has not been modified, chemically or otherwise, in any way.
  • Chemical modifications may also include derivatization of starch by reaction of its hydroxyl groups with alkylene oxides, and other ether-, ester-, urethane-, carbamate-, or isocyanate-forming substances. Hydroxyalkyl, ethersuccinylated, acetyl, or carbamate starches or mixtures thereof can be used as chemically modified starches.
  • the degree of substitution of the chemically modified starch is from 0.001 to 3.0, and more specifically from 0.003 to 0.2.
  • Biological modifications of starch may include bacterial digestion of the carbohydrate bonds, or enzymatic hydrolysis using enzymes such as amylase, amylopectase, and the like.
  • Suitable naturally occurring starches can include, but are not limited to: corn starch, potato starch, sweet potato starch, wheat starch, sago palm starch, tapioca starch, rice starch, soybean starch, arrow root starch, amioca starch, bracken starch, lotus starch, waxy maize starch, and high amylose corn starch.
  • Naturally occurring starches, particularly corn starch and wheat starch can be particularly beneficial due to their low cost and availability.
  • the molecular weight of the natural, unmodified starch may be reduced.
  • the optimum molecular weight is dependent on the type of starch used.
  • a starch with a low level of amylose component such as a waxy maize starch, disperses rather easily in an aqueous solution with the application of heat and does not retrograde or recrystallize significantly.
  • a waxy maize starch can be used at a weight average molecular weight, for example in the range of 500,000 g/mol to 40,000,000 g/mol.
  • Modified starches such as hydroxy-ethylated Dent corn starch, which contains about 25% amylose, or oxidized Dent corn starch tend to retrograde more than waxy maize starch but less than acid thinned starch. This retrogradation, or recrystallization, acts as a physical cross-linking to effectively raise the weight average molecular weight of the starch in aqueous solution. Therefore, an appropriate weight average molecular weight for a typical commercially available hydroxyethylated Dent corn starch with 2 wt. % hydroxyethylation or oxidized Dent corn starch is from about 200,000 g/mol to about 10,000,000 g/mol.
  • weight average molecular weights for ethoxylated starches with higher degrees of ethoxylation, for example a hydroxyethylated Dent corn starch with 5 wt % hydroxyethylation, weight average molecular weights of up to 40,000,000 g/mol may be suitable for the present invention.
  • the appropriate weight average molecular weight is from about 100,000 g/mol to about 15,000,000 g/mol.
  • the weight average molecular weight of starch may also be reduced to a desirable range for the present invention by physical/mechanical degradation (e.g., via the thermomechanical energy input of the processing equipment).
  • the natural starch can be hydrolyzed in the presence of an acid catalyst to reduce the molecular weight and molecular weight distribution of the composition.
  • the acid catalyst can be selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, citric acid, ammonium chloride and any combination thereof.
  • a chain scission agent may be incorporated into a spinnable starch composition such that the chain scission reaction takes place substantially concurrently with the blending of the starch with other components.
  • oxidative chain scission agents suitable for use herein include ammonium persulfate, hydrogen peroxide, hypochlorite salts, potassium permanganate, and mixtures thereof.
  • the chain scission agent is added in an amount effective to reduce the weight average molecular weight of the starch to the desirable range. It is found that compositions having modified starches in the suitable weight average molecular weight ranges have suitable shear viscosities, and thus improve processability of the composition. The improved processability is evident in less interruptions of the process (e.g., reduced breakage, shots, defects, hang-ups) and better surface appearance and strength properties of the final product, such as fibers of the present invention.
  • the fibrous element of the present invention is void of thermoplastic, water-insoluble polymers.
  • the fibrous element-forming polymers may be present in the aqueous hydroxyl polymer melt composition at an amount of from about 20% to about 50% and/or from about 30% to about 50% and/or from about 35% to about 48% by weight of the aqueous hydroxyl polymer melt composition and present in a polymeric structure, for example fibrous element and/or fibrous structure, at a level of from about 50% to about 100% and/or from about 60% to about 98% and/or from about 75% to about 95% by weight of the polymeric structure, for example fibrous element and/or fibrous structure.
  • the polymer melt compositions of the present invention and/or fibrous elements, such as filaments of the present invention may comprise, in addition to the fibrous element-forming polymer, other polymers, such as non-hydroxyl polymers.
  • Non-limiting examples of suitable non-hydroxyl polymers that may be included in the fibrous elements of the present invention include non-hydroxyl polymers that exhibit a weight average molecular weight of greater than 500,000 g/mol and/or greater than 750,000 g/mol and/or greater than 1,000,000 g/mol and/or greater than 1,250,000 g/mol and/or at greater than 1,400,000 g/mol and/or at least 1,450,000 g/mol and/or at least 1,500,000 g/mol and/or less than 10,000,000 g/mol and/or less than 5,000,000 g/mol and/or less than 2,500,00 g/mol and/or less than 2,000,000 g/mol and/or less than 1,750,000 g/mol.
  • the non-hydroxyl polymer exhibits a polydispersity of greater than 1.10 and/or at least 1.20 and/or at least 1.30 and/or at least 1.32 and/or at least 1.40 and/or at least 1.45.
  • Non-limiting examples of suitable non-hydroxyl polymers include polyacrylamide and derivatives such as carboxyl modified polyacrylamide polymers and copolymers including polyacrylic, poly(hydroxyethyl acrylic), polymethacrylic acid and their partial esters; vinyl polymers including polyvinylalcohol, polyvinylpyrrolidone, and the like; polyamides; polyalkylene oxides such as polyethylene oxide and mixtures thereof. Copolymers or graft copolymers made from mixtures of monomers selected from the aforementioned polymers are also suitable herein.
  • Non-limiting examples of commercially available polyacrylamides include nonionic polyacrylamides such as N300 from Kemira or Hyperfloc® NF221, NF301, and NF241 from Hychem, Inc.
  • the non-hydroxyl polymers may be present in an amount of from about 0.01% to about 10% and/or from about 0.05% to about 5% and/or from about 0.075% to about 2.5% and/or from about 0.1% to about 1%, by weight of the aqueous hydroxyl polymer melt composition, filament and/or fibrous structure.
  • the non-hydroxyl polymer comprises a linear polymer. In another example, the non-hydroxyl polymer comprises a long chain branched polymer. In still another example, the non-hydroxyl polymer is compatible with the hydroxyl polymer at a concentration greater than the non-hydroxyl polymer's entanglement concentration C e .
  • Non-limiting examples of suitable non-hydroxyl polymers are selected from the group consisting of: polyacrylamide and its derivatives; polyacrylic acid, polymethacrylic acid and their esters; polyethyleneimine; copolymers made from mixtures of the aforementioned polymers; and mixtures thereof.
  • the non-hydroxyl polymer comprises polyacrylamide.
  • the fibrous elements comprises two or more non-hydroxyl polymers, such as two or more polyacrylamides, such at two or more different weight average molecular weight polyacrylamides.
  • the non-hydroxyl polymer comprises an acrylamide-based copolymer.
  • the non-hydroxyl polymer comprises a polyacrylamide and an acrylamide-based copolymer.
  • the acrylamide-based copolymer is derived from an acrylamide monomer and at least one monomer selected from the group consisting of: pendant hydroxyl-containing monomers, pendant hydroxyl alkylether-containing monomers, pendant hydroxyl alkylester-containing monomers, pendant hydroxyl alkylamide-containing monomers, and mixtures thereof.
  • the acrylamide-based copolymer comprises an acrylamide monomeric unit and at least one monomeric unit selected from the group consisting of: pendant hydroxyl-containing monomeric units, pendant hydroxyl alkylether-containing monomeric units, pendant hydroxyl alkylester-containing monomeric units, pendant hydroxyl alkylamide-containing monomeric units, and mixtures thereof.
  • a crosslinking system comprising a crosslinking agent, such as an imidazolidinone, and optionally, a crosslinking facilitator, such as an ammonium salt, may be present in the polymer melt composition and/or may be added to the polymer melt composition before polymer processing of the polymer melt composition.
  • a crosslinking agent such as an imidazolidinone
  • a crosslinking facilitator such as an ammonium salt
  • Crosslinking agent as used herein means any material that is capable of crosslinking a hydroxyl polymer within a polymer melt composition according to the present.
  • suitable crosslinking agents include polycarboxylic acids and/or imidazolidinones, such as dihydroxyethyleneurea (DHEU).
  • DHEU dihydroxyethyleneurea
  • the crosslinking agent is in the form of a solution rather than a recrystallized form.
  • the crosslinking agent comprises less than 2% and/or less than 1.8% and/or less than 1.5% and/or less than 1.25% and/or 0% and/or to about 0.25% and/or to about 0.5% by weight of a base, such as triethanolamine.
  • Crosslinking facilitator as used herein means any material that is capable of activating a crosslinking agent thereby transforming the crosslinking agent from its unactivated state to its activated state.
  • the crosslinking agent Upon crosslinking the hydroxyl polymer during the curing step, the crosslinking agent becomes an integral part of the polymeric structure as a result of crosslinking the hydroxyl polymer as shown in the following schematic representation:
  • the crosslinking facilitator may include derivatives of the material that may exist after the transformation/activation of the crosslinking agent.
  • a crosslinking facilitator salt being chemically changed to its acid form and vice versa.
  • Non-limiting examples of suitable crosslinking facilitators include acids having a pKa of less than 6 or salts thereof.
  • the crosslinking facilitators may be Bronsted Acids and/or salts thereof, such as ammonium salts thereof.
  • metal salts such as magnesium and zinc salts
  • Bronsted Acids and/or salts thereof can be used alone or in combination with Bronsted Acids and/or salts thereof, as crosslinking facilitators.
  • Non-limiting examples of suitable crosslinking facilitators include benzoic acid, citric acid, formic acid, glycolic acid, lactic acid, maleic acid, phthalic acid, phosphoric acid, hypophosphoric acid, succinic acid, and mixtures thereof and/or their salts, such as their ammonium salts, such as ammonium glycolate, ammonium citrate, ammonium chloride, ammonium sulfate.
  • crosslinking facilitators include glyoxal bisulfate salts, primary amine salts, such as hydroxyethyl ammonium salts, hydroxypropyl ammonium salt, secondary amine salts, ammonium toluene sulfonate, ammonium benzene sulfonate, ammonium xylene sulfonate, magnesium chloride, and zinc chloride.
  • the polymer melt compositions of the present invention and/or fibrous elements of the present invention and fibrous structures formed thereform may comprise one or more surfactants.
  • the surfactant is a fast wetting surfactant.
  • the surfactant comprises a non-fast wetting surfactant, such as Aerosol® OT from Cytec.
  • Non-limiting examples of suitable fast wetting surfactants include surfactants that exhibit a twin-tailed general structure, for example a surfactant that exhibits a structure VIIA or VIIB as follows.
  • R is independently selected from substituted or unsubstituted, linear or branched aliphatic groups and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 4 -C 7 aliphatic chains and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 4 -C 7 alkyls and mixtures thereof and M is a suitable cation, such as an alkali metal cation and/or an ammonium cation.
  • R is independently selected from substituted or unsubstituted, linear or branched C 5 -C 6 alkyls and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 6 alkyls and mixtures thereof.
  • R is an unsubstituted, branched C 6 alkyl having the following structure VIII.
  • R is independently selected from substituted or unsubstituted, linear or branched C 5 alkyls and mixtures thereof.
  • R is independently selected from unsubstituted, linear C 5 alkyls and mixtures thereof.
  • the C 5 alkyl may comprise a mixture of unsubstituted linear C 5 alkyls, for example C 5 n-pentyl, and/or 1-methyl branched C 5 alkyls as shown in the following structure IX.
  • R comprises a mixture of C 4 -C 7 alkyls and/or a mixture of C 5 -C 6 alkyls.
  • the fast wetting surfactants may be present in the polymer melt compositions, fibrous elements, and/or fibrous structures of the present invention, alone or in combination with other non-fast wetting surfactants.
  • the fast wetting surfactants of the present invention may be used individually or in mixtures with each other or in a mixture with one or more non-fast wetting surfactants, for example a C 8 sulfosuccinate surfactant where R is the following structure X
  • a fast wetting surfactant comprises a sulfosuccinate surfactant having the following structure XI.
  • R is independently selected from substituted or unsubstituted, linear or branched aliphatic groups and mixtures thereof and M is a suitable cation, such as an alkali metal cation and/or an ammonium cation.
  • R is independently selected from substituted or unsubstituted, linear or branched C 4 -C 7 aliphatic chains and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 4 -C 7 alkyls and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 5 -C 6 alkyls and mixtures thereof.
  • R is independently selected from substituted or unsubstituted, linear or branched C 6 alkyls and mixtures thereof.
  • R is an unsubstituted, branched C 6 alkyl having the following structure XII.
  • Non-limiting examples of fast wetting surfactants according to the present invention include sulfosuccinate surfactants, for example a sulfosuccinate surfactant that has structure VIII as its R groups (Aerosol® MA-80), a sulfosuccinate surfactant that has C 4 isobutyl as its R groups (Aerosol® IB), and a sulfosuccinate surfactant that has a mixture of C 5 n-pentyl and structure IX as its R groups (Aerosol® AY), all commercially available from Cytec.
  • sulfosuccinate surfactants for example a sulfosuccinate surfactant that has structure VIII as its R groups (Aerosol® MA-80), a sulfosuccinate surfactant that has C 4 isobutyl as its R groups (Aerosol® IB), and a sulfosuccinate surfactant that has a mixture of C 5
  • fast wetting surfactants include alcohol sulfates derived from branched alcohols such as Isalchem and Lial alcohols (from Sasol) ie. Dacpon 27 23 AS and Guerbet alcohols from Lucky Chemical. Still another example of a fast wetting surfactant includes paraffin sulfonates such as Hostapur SAS30 from Clariant.
  • the fast wetting surfactants are present in an amount of from about 0.01% to about 5% and/or from about 0.5% to about 2.5% and/or from about 1% to about 2% and/or from about 1% to about 1.5%, by weight of the polymer melt composition, fibrous element and/or fibrous structure.
  • a fast wetting surfactant may be present both in the interior and exterior of the fibrous elements produced from the polymer melt composition, which is distinguished from a surface only treatment of the formed fibrous elements. Any fast wetting surfactant that is present on the exterior of a fibrous element may be determined by extracting the fibrous element with a solvent that dissolves the surfactant, but does not swell the fibrous element and then analyzing for the surfactant by LC-mass spec.
  • the surfactant that is present in the interior of the fibrous element may be determined by extracting the fibrous element with a solvent that dissolves the surfactant and also swells the fibrous elements, such as water/alcohol or water/acetone mixtures followed by analysis for surfactant by a technique such as LC mass spec.
  • the fibrous element may be treated with an enzyme such as amylase that degrades the fibrous element-forming polymer, for example polysaccharide, but not the fast wetting surfactant and the resulting solution may be analyzed for the surfactant by LC-mass spec.
  • the polymer melt compositions and/or fibrous elements of the present invention may comprise one or more hueing agents.
  • the total level of one or more hueing agents present within one or more, for example a plurality, of the fibrous elements of a fibrous structure of the present invention is less than 1% and/or less than 0.5% and/or less than 0.05% and/or less than 0.005% and/or greater than 0.00001% and/or greater than 0.0001% and/or greater than 0.001% by weight of the dry fibrous element and/or dry fibrous structure formed by fibrous elements containing the hueing agents.
  • the total level of one or more hueing agents present within one or more, for example a plurality, of the fibrous elements of a fibrous structure of the present invention is from about 0.0001% to about 0.5% and/or from about 0.0005% to about 0.05% and/or from about 0.001% to about 0.05% and/or from about 0.001% to about 0.005% by weight of the dry fibrous element and/or dry fibrous structure formed by fibrous elements containing the hueing agents.
  • Hueing agents can be used either alone or in combination.
  • Hueing agents may be selected from any known chemical class of dye, including but not limited to acridine, anthraquinone (including polycyclic quinones), azine, azo (e.g., monoazo, disazo, trisazo, tetrakisazo, polyazo), including premetallized azo, benzodifurane and benzodifuranone, carotenoid, coumarin, cyanine, diazahemicyanine, diphenylmethane, formazan, hemicyanine, indigoids, methane, naphthalimides, naphthoquinone, nitro and nitroso, oxazine, phthalocyanine, pyrazoles, stilbene, styryl, triarylmethane, triphenylmethane, xanthenes and mixtures thereof.
  • hueing agents include dyes, dye-clay conjugates, and organic and inorganic pigments and mixtures thereof.
  • Suitable dyes include small molecule dyes and polymeric dyes.
  • Suitable small molecule dyes include small molecule dyes selected from the group consisting of dyes falling into the Colour Index (C.I.) classifications of Direct, Basic, Reactive or hydrolysed Reactive, Solvent or Disperse dyes for example that are classified as Blue, Violet, Red, Green or Black, and mixtures thereof.
  • suitable small molecule dyes include small molecule dyes selected from the group consisting of Colour Index (Society of Dyers and Colourists, Bradford, UK) numbers Direct Violet dyes such as 9, 35, 48, 51, 66, and 99, Direct Blue dyes such as 1, 71, 80 and 279, Acid Red dyes such as 17, 73, 52, 88 and 150, Acid Violet dyes such as 15, 17, 24, 43, 49 and 50, Acid Blue dyes such as 15, 17, 25, 29, 40, 45, 75, 80, 83, 90 and 113, Acid Black dyes such as 1, Basic Violet dyes such as 1, 3, 4, 10 and 35, Basic Blue dyes such as 3, 16, 22, 47, 66, 75 and 159, Disperse or Solvent dyes such as those described in US 2008/034511 A1 or U.S.
  • Colour Index Society of Dyers and Colourists, Bradford, UK
  • Direct Violet dyes such as 9, 35, 48, 51, 66, and 99
  • Direct Blue dyes such as 1, 71, 80 and 279
  • suitable small molecule dyes include small molecule dyes selected from the group consisting of C.I. Acid Violet 17, Direct Blue 71, Direct Violet 51, Direct Blue 1, Acid Red 88, Acid Red 150, Acid Blue 29, Acid Blue 113 or mixtures thereof.
  • Suitable polymeric dyes include polymeric dyes selected from the group consisting of polymers containing covalently bound (sometimes referred to as conjugated) chromogens, (dye-polymer conjugates), for example polymers with chromogens co-polymerized into the backbone of the polymer and mixtures thereof.
  • Polymeric dyes include those described in WO2011/98355, US 2012/225803 A1, US 2012/090102 A1, U.S. Pat. No. 7,686,892 B2, and WO2010/142503.
  • suitable polymeric dyes include polymeric dyes selected from the group consisting of hueing agents commercially available under the trade name of Liquitint® (Milliken, Spartanburg, S.C., USA), dye-polymer conjugates formed from at least one reactive dye and a polymer selected from the group consisting of polymers comprising a moiety selected from the group consisting of a hydroxyl moiety, a primary amine moiety, a secondary amine moiety, a thiol moiety and mixtures thereof.
  • Liquitint® Moquitint®
  • dye-polymer conjugates formed from at least one reactive dye and a polymer selected from the group consisting of polymers comprising a moiety selected from the group consisting of a hydroxyl moiety, a primary amine moiety, a secondary amine moiety, a thiol moiety and mixtures thereof.
  • suitable polymeric dyes include polymeric dyes selected from the group consisting of Liquitint® Violet CT, carboxymethyl cellulose (CMC) covalently bound to a reactive blue, reactive violet or reactive red dye such as CMC conjugated with C.I. Reactive Blue 19, sold by Megazyme, Wicklow, Ireland under the product name AZO-CM-CELLULOSE, product code S-ACMC, alkoxylated triphenyl-methane polymeric colourants, alkoxylated thiophene polymeric colourants, and mixtures thereof.
  • CMC carboxymethyl cellulose
  • the fibrous structures of the present invention may further comprise one or more solid additives.
  • Solid additive as used herein means an additive that is capable of being applied to a surface of a fibrous structure and/or nonwoven substrate of the fibrous structure in a solid form.
  • the solid additive of the present invention can be delivered directly to a surface of the fibrous structure and/or nonwoven substrate of the fibrous structure without a liquid phase being present, i.e. without melting the solid additive and without suspending the solid additive in a liquid vehicle or carrier.
  • the solid additive of the present invention does not require a liquid state or a liquid vehicle or carrier in order to be delivered to a surface of a nonwoven substrate.
  • the solid additive of the present invention may be delivered via a gas or combinations of gases.
  • a solid additive is an additive that when placed within a container, does not take the shape of the container.
  • a solid additive comprises a naturally occurring fiber, such as a pulp fiber.
  • the solid additives of the present invention may have different geometries and/or cross-sectional areas that include round, elliptical, star-shaped, rectangular, trilobal and other various eccentricities.
  • the solid additive may exhibit a particle size of less than 6 mm and/or less than 5.5 mm and/or less than 5 mm and/or less than 4.5 mm and/or less than 4 mm and/or less than 2 mm in its maximum dimension.
  • Particle as used herein means an object having an aspect ratio of less than about 25/1 and/or less than about 15/1 and/or less than about 10/1 and/or less than 5/1 to about 1/1.
  • a particle is not a fiber as defined herein.
  • the solid additives may be present in the fibrous structures of the present invention at a level of greater than about 1 and/or greater than about 2 and/or greater than about 4 and/or to about 20 and/or to about 15 and/or to about 10 g/m 2 .
  • a fibrous structure of the present invention comprises from about 2 to about 10 and/or from about 5 to about 10 g/m 2 of solid additive.
  • the solid additives are present in the fibrous structures of the present invention at a level of greater than 5% and/or greater than 10% and/or greater than 20% to about 50% and/or to about 40% and/or to about 30%.
  • the fibrous structures of the present invention may further comprise a scrim material.
  • the scrim material may comprise any suitable material capable of bonding to a nonwoven substrate of the fibrous structure of the present invention.
  • the scrim material comprises a material that can be thermally bonded to the nonwoven substrate of the fibrous structure of the present invention.
  • suitable scrim materials include filaments of the present invention.
  • the scrim material comprises filaments that comprise hydroxyl polymers.
  • the scrim material comprises starch filaments.
  • the scrim material comprises filaments comprising a thermoplastic polymer.
  • the scrim material comprises a fibrous structure according to the present invention wherein the fibrous structure comprises filaments comprising hydroxyl polymers, such as starch filaments, and/or thermoplastic polymers.
  • the scrim material may comprise a film.
  • the scrim material may comprise a nonwoven substrate according to the present invention.
  • the scrim material may comprise a latex.
  • the scrim material may be the same composition as the nonwoven substrate of the fibrous structure.
  • the scrim material and/or an exterior layer comprising a plurality of hydroxyl polymer fibrous elements of the fibrous structure may be present in the fibrous structures of the present invention at a basis weight of greater than 6 and/or greater than 8 and/or greater than 10 and/or greater than 12 and/or greater than 14 and/or greater than 16 and/or greater than 18 and/or less than 40 and/or less than 35 and/or less than 30 and/or less than 25 g/m 2 (“gsm”) and/or from about 12 to about 40 g/m 2 and/or from about 12 to about 35 g/m 2 and/or from about 12 to about 30 g/m 2 and/or from about 16 to about 25 g/m 2 .
  • the basis weight of the scrim material and/or exterior layer or other layers of the fibrous structure are known by the manufacturer when making the fibrous structure and may be determined by other means such as tape stripping or other suitable means known to those in the art.
  • the methods of the present invention relate to producing fibrous structures comprising fibrous elements produced from polymer melt compositions comprising a fibrous element-forming polymer, such as a hydroxyl polymer, a crosslinking agent, an acrylamide-based copolymer, and other materials as described herein.
  • a fibrous element-forming polymer such as a hydroxyl polymer, a crosslinking agent, an acrylamide-based copolymer, and other materials as described herein.
  • FIGS. 1 and 2 illustrate one example of a method for making a fibrous structure of the present invention. As shown in FIGS. 1 and 2 , the method 10 comprises the steps of:
  • first hydroxyl polymer fibrous elements for example hydroxyl polymer filaments, 12 from a first source 14 of hydroxyl polymer fibrous elements, which form a first layer 16 of hydroxyl polymer fibrous elements;
  • second hydroxyl polymer fibrous elements for example hydroxyl polymer filaments, 18 from a second source 20 of hydroxyl polymer fibrous elements, which form a second layer 22 of hydroxyl polymer fibrous elements;
  • third hydroxyl polymer fibrous elements for example hydroxyl polymer filaments, 24 from a third source 26 of hydroxyl polymer fibrous elements, which form a third layer 28 of hydroxyl polymer fibrous elements;
  • fourth hydroxyl polymer fibrous elements for example hydroxyl polymer filaments, 34 from a fourth source 36 of hydroxyl polymer fibrous elements, which form a fourth layer 38 of hydroxyl polymer fibrous elements;
  • first, second, third, and fourth hydroxyl polymer fibrous elements 12 , 18 , 24 , 34 and the solid additives 30 to form a fibrous structure 40 , wherein the first source 14 of hydroxyl polymer fibrous elements is oriented at a first angle ⁇ to the machine direction of the fibrous structure 40 , the second source 20 of hydroxyl polymer fibrous elements is oriented at a second angle ⁇ to the machine direction different from the first angle ⁇ , the third source 26 is oriented at a third angle ⁇ to the machine direction different from the first angle ⁇ and the second angle ⁇ , and wherein the fourth source 36 is oriented at a fourth angle ⁇ to the machine direction different from the second angle ⁇ and third angle ⁇ .
  • the first, second, and third layers 16 , 22 , 28 of hydroxyl polymer fibrous elements are collected on a collection device 42 , which may be a belt or fabric, with or without the aid of a vacuum box 47 .
  • the collection device 42 may be a patterned belt that imparts a pattern, such as a non-random, repeating pattern to the fibrous structure 40 during the fibrous structure making process.
  • the first, second, and third layers 16 , 22 , 28 of hydroxyl polymer fibrous elements are collected (for example one on top of the other) on the collection device 42 to form a multi-layer nonwoven substrate 44 upon which the solid additives 30 are deposited.
  • the fourth layer 38 of hydroxyl polymer fibrous elements may then be deposited onto the solid additives 30 to form a scrim 46 .
  • the first angle ⁇ and the fourth angle ⁇ may be the same angle, for example 90° to the machine direction.
  • the second angle ⁇ and the third angle ⁇ may be the same angle, just positive and negative of one another.
  • the second angle ⁇ may be ⁇ 40° to the machine direction and the third angle ⁇ may be +40° to the machine direction.
  • At least one of the first, second, and third angles ⁇ , ⁇ , ⁇ is less than 90° to the machine direction.
  • the first angle ⁇ and/or fourth angle ⁇ is about 90° to the machine direction.
  • the second angle ⁇ and/or third angle ⁇ is from about ⁇ 10° to about ⁇ 80° and/or from about ⁇ 30° to about ⁇ 60° to the machine direction and/or about ⁇ 40° to the machine direction.
  • the first, second, and third layers 16 , 22 , 28 of filaments may be formed into a nonwoven substrate 44 prior to being utilized in the process for making a fibrous structure described above.
  • the nonwoven substrate 44 would likely be in a parent roll that could be unwound into the fibrous structure making process and the solid additives 30 could be deposited directly onto a surface of the nonwoven substrate 44 .
  • the step of providing a plurality of solid additives 30 onto the nonwoven substrate 44 may comprise airlaying the solid additives 30 using an airlaying former.
  • an airlaying former is available from Dan-Web of Aarhus, Denmark.
  • the step of providing fourth filaments 34 such that the filaments contact the solid additives 30 comprises the step of depositing the fourth filaments 34 such that at least a portion (in one example all or substantially all) of the solid additives 30 are contacted by the fourth filaments 34 thus positioning the solid additives 30 between the fourth layer 38 of filaments and the nonwoven substrate 44 .
  • the fibrous structure 40 may be subjected to a bonding step that bonds the fourth layer 38 of filaments (in this case, the scrim 46 ) to the nonwoven substrate 44 .
  • This step of bonding may comprise a thermal bonding operation.
  • the thermal bonding operation may comprise passing the fibrous structure 40 through a nip formed by thermal bonding rolls 48 , 50 . At least one of the thermal bonding rolls 48 , 50 may comprise a pattern that is translated into the bond sites 52 formed in the fibrous structure 40 .
  • the fibrous structure may also be subjected to other post-processing operations such as embossing, tuft-generating, gear rolling, which includes passing the fibrous structure through a nip formed between two engaged gear rolls, moisture-imparting operations, free-fiber end generating, and surface treating to form a finished fibrous structure.
  • the fibrous structure is subjected to gear rolling by passing the fibrous structure through a nip formed by at least a pair of gear rolls.
  • the fibrous structure is subjected to gear rolling such that free-fiber ends are created in the fibrous structure.
  • the gear rolling may occur before or after two or more fibrous structures are combined to form a multi-ply sanitary tissue product. If it occurs after, then the multi-ply sanitary tissue product is passed through the nip formed by at least a pair of gear rolls.
  • the method for making a fibrous structure of the present invention may be close coupled (where the fibrous structure is convolutedly wound into a roll prior to proceeding to a converting operation) or directly coupled (where the fibrous structure is not convolutedly wound into a roll prior to proceeding to a converting operation) with a converting operation to emboss, print, deform, surface treat, or other post-forming operation known to those in the art.
  • direct coupling means that the fibrous structure can proceed directly into a converting operation rather than, for example, being convolutedly wound into a roll and then unwound to proceed through a converting operation.
  • one or more plies of the fibrous structure according to the present invention may be combined, for example with glue, with another ply of fibrous structure, which may also be a fibrous structure according to the present invention, to form a multi-ply sanitary tissue product.
  • the multi-ply sanitary tissue product may be formed by combining two or more plies of fibrous structure according to the present invention.
  • two or more plies of fibrous structure according to the present invention may be combined to form a multi-ply sanitary tissue product such that the solid additives present in the fibrous structure plies are adjacent to each of the outer surfaces of the multi-ply sanitary tissue product.
  • the process of the present invention may include preparing individual rolls of fibrous structure and/or sanitary tissue product comprising such fibrous structure(s) that are suitable for consumer use.
  • the process may utilize a single source of fibrous elements and/or multiple (greater than 4) sources of fibrous elements and the fibrous structure may be a single layer or multiple layers depending on the number of sources of fibrous elements and/or sources of solid additives.
  • the sources of filaments comprise meltblow dies that produce filaments from a polymer melt composition according to the present invention.
  • the meltblow die 54 may comprise at least one fibrous element-forming hole 56 , and/or 2 or more and/or 3 or more rows of fibrous element-forming holes 56 from which filaments are spun. At least one row of the fibrous element-forming holes 56 contains 2 or more and/or 3 or more and/or 10 or more fibrous element-forming holes 56 .
  • the meltblow die 54 comprises fluid-releasing holes 58 , such as gas-releasing holes, in one example air-releasing holes, that provide attenuation to the filaments formed from the fibrous element-forming holes 56 .
  • fluid-releasing holes 58 may be associated with a fibrous element-forming hole 56 such that the fluid exiting the fluid-releasing hole 58 is parallel or substantially parallel (rather than angled like a knife-edge die) to an exterior surface of a filament exiting the fibrous element-forming hole 56 .
  • the fluid exiting the fluid-releasing hole 58 contacts the exterior surface of a filament formed from a fibrous element-forming hole 56 at an angle of less than 30° and/or less than 20° and/or less than 10° and/or less than 5° and/or about 0°.
  • One or more fluid releasing holes 58 may be arranged around a fibrous element-forming hole 56 .
  • one or more fluid-releasing holes 58 are associated with a single fibrous element-forming hole 56 such that the fluid exiting the one or more fluid releasing holes 58 contacts the exterior surface of a single filament formed from the single fibrous element-forming hole 56 .
  • the fluid-releasing hole 58 permits a fluid, such as a gas, for example air, to contact the exterior surface of a filament formed from a fibrous element-forming hole 56 rather than contacting an inner surface of a filament, such as what happens when a hollow filament is formed.
  • a fluid such as a gas, for example air
  • the polymer melt composition for example an aqueous polymer melt composition such as an aqueous hydroxyl polymer melt composition, of the present invention comprises a melt processed fibrous element-forming polymer, such as a melt processed hydroxyl polymer, and a fast wetting surfactant according to the present invention.
  • the polymer melt compositions may already be formed or a melt processing step may need to be performed to convert a raw material fibrous element-forming polymer, such as a hydroxyl polymer, into a melt processed fibrous element-forming polymer, such as a melt processed hydroxyl polymer, thus producing the polymer melt composition.
  • Any suitable melt processing step known in the art may be used to convert the raw material fibrous element-forming polymer into the melt processed fibrous element-forming polymer.
  • Melt processing as used herein means any operation and/or process by which a polymer is softened to such a degree that it can be brought into a flowable state.
  • the polymer melt compositions may have a temperature of from about 50° C. to about 100° C. and/or from about 65° C. to about 95° C. and/or from about 70° C. to about 90° C. when spinning fibrous elements from the polymer melt compositions.
  • the polymer melt composition of the present invention may comprise from about 30% and/or from about 40% and/or from about 45% and/or from about 50% to about 75% and/or to about 80% and/or to about 85% and/or to about 90% and/or to about 95% and/or to about 99.5% by weight of the polymer melt composition of a fibrous element-forming polymer, such as a hydroxyl polymer.
  • the fibrous element-forming polymer such as a hydroxyl polymer, may have a weight average molecular weight greater than 100,000 g/mol
  • the fibrous elements and/or fibrous structure of the present invention produced via a polymer processing operation may be cured at a curing temperature of from about 110° C. to about 260° C. and/or from about 110° C. to about 230° C. and/or from about 120° C. to about 200° C. and/or from about 130° C. to about 185° C. for a time period of from about 0.01 and/or 1 and/or 5 and/or 15 seconds to about 60 minutes and/or from about 20 seconds to about 45 minutes and/or from about 30 seconds to about 30 minutes.
  • Alternative curing methods may include radiation methods such as UV, e-beam, IR and other temperature-raising methods.
  • the polymeric structure may also be cured at room temperature for days, either after curing at above room temperature or instead of curing at above room temperature.
  • the polymeric structures of the present invention may include melt spun fibers and/or spunbond fibers, staple fibers, hollow fibers, shaped fibers, such as multi-lobal fibers and multicomponent fibers, especially bicomponent fibers.
  • the multicomponent fibers, especially bicomponent fibers may be in a side-by-side, sheath-core, segmented pie, ribbon, islands-in-the-sea configuration, or any combination thereof.
  • the sheath may be continuous or non-continuous around the core.
  • the ratio of the weight of the sheath to the core can be from about 5:95 to about 95:5.
  • the fibers of the present invention may have different geometries that include round, elliptical, star shaped, rectangular, and other various eccentricities.
  • One or more polymeric structures of the present invention may be incorporated into a multi-polymeric structure product, such as a fibrous structure and/or web, if the polymeric structures are in the form of fibers.
  • a multi-polymeric structure product may ultimately be incorporated into a commercial product, such as a single- or multi-ply sanitary tissue product, such as facial tissue, bath tissue, paper towels and/or wipes, feminine care products, diapers, writing papers, cores, such as tissue cores, and other types of paper products.
  • a polymer melt composition comprising 79% IPG starch commercially available from Ingredion Inc., 16% Ethylex 2035 (ethoxylated starch) commercially available from Tate & Lyle PLC, 0.6% Aerosol AOT-70PG (sulfosuccinate surfactant) available from Cytec Industries, Inc., 0.6% Hyperfloc NF301PWG (non-hydroxyl polymer), commercially available from Hychem Inc., 3.1% Urea glyoxal adduct crosslinking agent (dihydroxyethyleneurea) (containing less than 2% by weight of a base, for example triethanolamine), 0.003% Violet CT (hueing agent) commercially available from Milliken Chemical, and 0.7% Ammonium methane sulfonate (crosslinking facilitator).
  • IPG starch commercially available from Ingredion Inc.
  • Ethylex 2035 ethoxylated starch
  • Aerosol AOT-70PG sulfosuccinate surfact
  • the polymer melt composition is cooked at approximately 125° C. and extruded from a co-rotating twin screw extruder at approx 50% solids (50% H 2 O).
  • the melt composition then passes through a heat exchanger to raise the temperature to approximately 175° C.
  • the heated melt then passes to a flash extruder where water is flashed off and the melt cooled back to approximately 70° C.
  • melt composition is then pumped to a meltblown spinnerette and attenuated with a 65° C. saturated air stream to form a nonwoven substrate having a basis weight of from about 10 g/m 2 to about 100 g/m 2 .
  • the filaments are then dried by convection drying before being deposited on a forming belt to form a filament web.
  • meltblown filaments are essentially continuous filaments.
  • Wood pulp fibers Southern Softwood Kraft available as roll comminution pulp, is disintegrated by a hammermill and conveyed to an airlaid former via a blower.
  • the wood pulp fibers are deposited onto the nonwoven substrate as a solid additive at a basis weight of from about 5 to 35 gsm.
  • the melt composition is also pumped to a second meltblown spinnerette and attenuated with a 65° C. saturated air stream to form a nonwoven substrate having a basis weight of from about 10 g/m 2 to about 100 g/m 2 .
  • the filaments are then dried by convection drying before being deposited on the web already in process as described above. These meltblown filaments are essentially continuous filaments.
  • the entire fibrous structure (sandwich) is then subjected to a thermal bonding process wherein the bond sites are formed with heat and pressure.
  • the bonded structure then undergoes a curing/crosslinking step by applying heat to the fibrous structure such that the fibrous structure reaches a temperature of about 200° C. for a sufficient time for sufficient crosslinking to occur.
  • the fibrous structure is then humidified to approximately 7-10 wt % moisture and rewound into a parent roll.
  • the single ply parent roll is then converted into a sanitary tissue product with perforations and an emboss pattern.
  • a polymer melt composition comprising 79% IPG starch commercially available from Ingredion Inc., 16% Ethylex 2035 (ethoxylated starch) commercially available from Tate & Lyle PLC, 0.6% Aerosol AOT-70PG (sulfosuccinate surfactant) available from Cytec Industries, Inc., 0.6% Hyperfloc NF301PWG (non-hydroxyl polymer), commercially available from Hychem Inc., 3.1% Urea glyoxal adduct crosslinking agent (dihydroxyethyleneurea) (containing less than 2% by weight of a base, for example triethanolamine), 0.003% Violet CT (hueing agent) commercially available from Milliken Chemical, and 0.7% Ammonium methane sulfonate (crosslinking facilitator).
  • IPG starch commercially available from Ingredion Inc.
  • Ethylex 2035 ethoxylated starch
  • Aerosol AOT-70PG sulfosuccinate surfact
  • the polymer melt composition is cooked at approximately 125° C. and extruded from a co-rotating twin screw extruder at approx 50% solids (50% H 2 O).
  • the melt composition then passes through a heat exchanger to raise the temperature to approximately 175° C.
  • the heated melt then passes to a flash extruder where water is flashed off and the melt cooled back to approximately 70° C.
  • the melt composition is then pumped to a meltblown spinnerette (meltblow die) and attenuated with a 65° C. saturated air stream to form a nonwoven substrate having a basis weight of from about 2 g/m 2 to about 25 g/m 2 .
  • the filaments are then dried by convection drying before being deposited on a first web material (a pre-formed cellulosic web) to form a fibrous structure according to the present invention.
  • the meltblown filaments in the fibrous structure are essentially continuous filaments.
  • the first web material (pre-formed cellulosic web) of the fibrous structure has a basis weight of from about 10 gsm to about 50 gsm. It is produced from a wet laid papermaking process commonly known in the art.
  • the cellulosic web can be made creped or uncreped, patterned or unpatterned.
  • the fibrous structure is then subjected to a thermal bonding process wherein the thermal bond sites are formed with heat and pressure.
  • the thermally bonded fibrous structure then undergoes a curing/crosslinking step by applying heat to the thermally bonded fibrous structure such that the thermally bonded fibrous structure reaches a temperature of about 200° C. for a sufficient time for sufficient crosslinking of the crosslinking agent in the filaments to occur.
  • the fibrous structure is then humidified to approximately 7-10 wt % moisture and rewound into a parent roll.
  • the single ply parent roll is then converted into a sanitary tissue product with perforations and an emboss pattern.
  • two parent rolls may be used to convert into a 2 ply sanitary tissue product.
  • meltblown filaments forming the exterior surfaces of the multi-ply sanitary tissue product.
  • Basis weight of a fibrous structure is measured on stacks of twelve usable units using a top loading analytical balance with a resolution of ⁇ 0.001 g.
  • the balance is protected from air drafts and other disturbances using a draft shield.
  • a precision cutting die, measuring 8.890 cm ⁇ 0.00889 cm by 8.890 cm ⁇ 0.00889 cm is used to prepare all samples.
  • the Basis Weight is calculated in g/m 2 as follows:
  • Basis Weight (Mass of stack)/[(Area of 1 square in stack) ⁇ (No. of squares in stack)]
  • Basis Weight (g/m 2 ) Mass of stack (g)/[79.032 (cm 2 )/10,000 (cm 2 /m 2 ) ⁇ 12]
  • Sample dimensions can be changed or varied using a similar precision cutter as mentioned above, so as at least 645 square centimeters of sample area is in the stack.
  • a fibrous structure comprising filaments of appropriate basis weight (approximately 5 to 20 grams/square meter) is cut into a rectangular shape sample, approximately 20 mm by 35 mm.
  • the sample is then coated using a SEM sputter coater (EMS Inc, PA, USA) with gold so as to make the filaments relatively opaque. Typical coating thickness is between 50 and 250 nm.
  • the sample is then mounted between two standard microscope slides and compressed together using small binder clips.
  • the sample is imaged using a 10 ⁇ objective on an Olympus BHS microscope with the microscope light-collimating lens moved as far from the objective lens as possible. Images are captured using a Nikon D1 digital camera.
  • a Glass microscope micrometer is used to calibrate the spatial distances of the images.
  • the approximate resolution of the images is 1 ⁇ m/pixel. Images will typically show a distinct bimodal distribution in the intensity histogram corresponding to the filaments and the background. Camera adjustments or different basis weights are used to achieve an acceptable bimodal distribution. Typically 10 images per sample are taken and the image analysis results averaged.
  • the images are analyzed in a similar manner to that described by B. Pourdeyhimi, R. and R. Dent in “Measuring fiber diameter distribution in nonwovens” (Textile Res. J. 69(4) 233-236, 1999).
  • Digital images are analyzed by computer using the MATLAB (Version. 6.1) and the MATLAB Image Processing Tool Box (Version 3.)
  • the image is first converted into a grayscale.
  • the image is then binarized into black and white pixels using a threshold value that minimizes the intraclass variance of the thresholded black and white pixels. Once the image has been binarized, the image is skeltonized to locate the center of each fiber in the image. The distance transform of the binarized image is also computed.
  • the scalar product of the skeltonized image and the distance map provides an image whose pixel intensity is either zero or the radius of the fiber at that location. Pixels within one radius of the junction between two overlapping fibers are not counted if the distance they represent is smaller than the radius of the junction. The remaining pixels are then used to compute a length-weighted histogram of filament diameters contained in the image.
  • TS7 and TS750 values are measured using an EMTEC Tissue Softness Analyzer (“Emtec TSA”) (Emtec Electronic GmbH, Leipzig, Germany) interfaced with a computer running Emtec TSA software (version 3.19 or equivalent).
  • Emtec the TS7 value correlates with the real material softness
  • TS750 value correlates with the felt smoothness/roughness of the material.
  • the Emtec TSA comprises a rotor with vertical blades which rotate on the test sample at a defined and calibrated rotational speed (set by manufacturer) and contact force of 100 mN. Contact between the vertical blades and the test piece creates vibrations, which create sound that is recorded by a microphone within the instrument. The recorded sound file is then analyzed by the Emtec TSA software. The sample preparation, instrument operation and testing procedures are performed according the instrument manufacture's specifications.
  • Test samples are prepared by cutting square or circular samples from a finished product. Test samples are cut to a length and width (or diameter if circular) of no less than about 90 mm, and no greater than about 120 mm, in any of these dimensions, to ensure the sample can be clamped into the TSA instrument properly. Test samples are selected to avoid perforations, creases or folds within the testing region. Prepare 8 substantially similar replicate samples for testing. Equilibrate all samples at TAPPI standard temperature and relative humidity conditions (23° C. ⁇ 2 C.° and 50% ⁇ 2%) for at least 1 hour prior to conducting the TSA testing, which is also conducted under TAPPI conditions.
  • test sample into the instrument, and perform the test according to the manufacturer's instructions.
  • the software displays values for TS7 and TS750. Record each of these values to the nearest 0.01 dB V 2 rms.
  • the test piece is then removed from the instrument and discarded. This testing is performed individually on the top surface (outer facing surface of a rolled product) of four of the replicate samples, and on the bottom surface (inner facing surface of a rolled product) of the other four replicate samples.
  • the four test result values for TS7 and TS750 from the top surface are averaged (using a simple numerical average); the same is done for the four test result values for TS7 and TS750 from the bottom surface. Report the individual average values of TS7 and TS750 for both the top and bottom surfaces on a particular test sample to the nearest 0.01 dB V 2 rms. Additionally, average together all eight test value results for TS7 and TS750, and report the overall average values for TS7 and TS750 on a particular test sample to the nearest 0.01 dB V 2 rms.
  • Sample strips (a total of 4 if testing both sides, 2 if testing a single side) of fibrous structures and/or sanitary tissue products, which do not have abraded portions) 11.43 cm (4.5 inch) wide ⁇ 30.48 cm to 40.64 cm (12-16 inch) long such that each sample strip can be folded upon itself to form a 11.43 cm (4.5 inch) wide (CD) by 10.16 cm (4.0 inch) long (MD) rectangular implement having a total basis weight of between 140 to 200 g/m 2 are obtained and conditioned according to Tappi Method #T402OM-88. For both side testing, makeup two rectangular implements as described above with a first side out and then two rectangular implements with the other side out (keep track of which are which).
  • this test can be used to make a lint measurement on the multi-ply sanitary tissue product, or, if the plies can be separated without damaging the sanitary tissue product, a measurement can be taken on the individual plies making up the sanitary tissue product. If a given sample differs from surface to surface, it is necessary to test both surfaces and average the scores in order to arrive at a composite lint score. In some cases, sanitary tissue products are made from multiple-plies of fibrous structures such that the facing-out surfaces are identical, in which case it is only necessary to test one surface.
  • Each sample is folded upon itself to make a 4.5′′ CD ⁇ 4′′ MD sample.
  • a smooth surface foam pad (1 ⁇ 8′′ thick, Poron quick Recovery Foam, adhesive back, firmness rating 13 ), having a length greater than or equal to 15.24 cm (6 inch) and a width greater than or equal to 12.70 cm (5 inch), to a flat and level table surface, positioned in such a way that its ⁇ 12.70 cm length direction is parallel to the table edge, and is flush with the table edge.
  • a piece of fine grade sandpaper (12.70 cm ⁇ 15.24 cm, using double-sided tape or glue), with its shorter axis parallel to the table edge, and centered with respect to other dimensions of the foam.
  • the felt is to be used in association with a weight.
  • the weight may include a clamping device to attach the felt/cardboard combination to the weight.
  • the weight and any clamping device total five (5) pounds.
  • the weight is available from Danilee Company, San Antonio, Tex., and is associated with the Sutherland Rub Tester.
  • the weight has a 2′′ ⁇ 4′′ piece of smooth surface foam attached to its contact face (1 ⁇ 8′′ thick, Poron quick Recovery Foam, adhesive back, firmness rating 13 ).
  • the felt is clamped directly against this foam surface, providing an effective contact area of 8 in 2 and a contact pressure of about 0.625 psi.
  • an additional 1′′ ⁇ 4′′ foam strip (same foam as described above) is attached and centered in the length direction on top the 2′′ ⁇ 4′′ foam strip, thus, after clamping the felt against this surface, an effective contact area of 4 in 2 and a contact pressure of about 1.25 psi is established.
  • two strips of tape (41 ⁇ 4′′-51 ⁇ 4′′ in length, Scotch brand 3 ⁇ 4′′ width) are placed along each edge of the felt (parallel to the long side of the felt) on the felt side that will be contacting the sample.
  • the untaped felt between the two tape strips has a width between 18-21 mm.
  • Three marks are placed on one of the strips of tape at 0, 4 and 10 centimeters along the flat, test region of the test felt.
  • the amount of dry lint and/or dry pills generated from a fibrous product according to the present invention is determined with a Sutherland Rub Tester (available from Danilee Company, San Antonio, Tex.). This tester uses a motor to rub a felt/weight component 5 times (back and forth) over the fibrous product, while the fibrous product is restrained in a stationary position.
  • a Sutherland Rub Tester available from Danilee Company, San Antonio, Tex.
  • Wet lint/pills are determined by pulling, during one pass, a partially wetted felt/weight component over a sample.
  • the next step is to complete image capture, analysis, and calculations on the test felts as described below.
  • the images of the felt (untested), sample (untested) and felt (tested) are captured using a computer and scanner (Microtek ArtixScan 1800f). Be certain that scanner glass is clear and clean. Place felts centered on scanner, face down. Adjust image capture boundaries so that all felts are included into the captured image. Set-up the scanner to 600 dpi, RGB, and 100% image size (no scaling). After successfully imaging the felts, save the image as an 8-bit RGB TIFF image, remove felts from scanner, and repeat from process until all felts images are captured.
  • Additional images of the sample (untested) may need to be captured (in the same manner) if they have an average luminance (using Optimas software) significantly less than 254 (less than 244), after being converted to an 8-bit gray-scale image. Also, an image of a known length standard (e.g., a ruler) is taken (exposure difference does not matter for this image). This image is used to calibrate the image analysis software distance scale.
  • Optimas software significantly less than 254 (less than 244)
  • the images captured are analyzed using Optimas 6.5 Image Analysis software commercially available from Media Cybernetics, L.P. Imaging set-up parameters, as listed herein, must be strictly adhered to in order to have meaningfully comparative lint score and pill score results.
  • an image with a known length standard is brought up in Optimas, and used to calibrate length units (millimeters in this case).
  • a known length standard e.g., a ruler
  • the region of interest (ROI) area is approximately 4500 mm2 (90 mm by 50 mm)
  • the wetted and dragged ROI area is approximately 1500 mm2 (94 mm by 16 mm).
  • the exact ROI area is measured and recorded (variable name: ROI area).
  • the average gray value of the unrubbed region of the test felt is used as the baseline, and is recorded for determining the threshold and lint values (variable name: untested felt GV avg).
  • Pills are determined as follows: Optimas creates boundary lines in the image where pixel luminance values cross through the threshold value (e.g., if the threshold is 120, boundary lines are created where pixels of higher and lower value exist on either side.
  • the criteria for determining a pill is that it must have an average luminance greater than the threshold value, and have a perimeter length greater than 0.5 mm.
  • the sum of the pilled areas variable name is: Total Pilled Area.
  • Measurement data of the ROI, and for each pill is exported from Optimas to a spreadsheet for performing the following calculations.
  • Lint Score Gray value difference between unpilled area of the rubbed test felt area and the untested felt
  • unpilled felt Gray Value avg [(ROI Gray Value avg*ROI area) ⁇ (pilled Gray Value avg*pilled area)]/Total Unpilled Area
  • the lint is obtained which is applicable to that particular web or product.
  • the following formula is used:

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