WO2000038565A1 - Multi-ply wipe - Google Patents
Multi-ply wipe Download PDFInfo
- Publication number
- WO2000038565A1 WO2000038565A1 PCT/US1999/031289 US9931289W WO0038565A1 WO 2000038565 A1 WO2000038565 A1 WO 2000038565A1 US 9931289 W US9931289 W US 9931289W WO 0038565 A1 WO0038565 A1 WO 0038565A1
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- WO
- WIPO (PCT)
- Prior art keywords
- basesheet
- fibers
- layer
- polyethylene
- layers
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
- A47L13/00—Implements for cleaning floors, carpets, furniture, walls, or wall coverings
- A47L13/10—Scrubbing; Scouring; Cleaning; Polishing
- A47L13/16—Cloths; Pads; Sponges
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4374—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece using different kinds of webs, e.g. by layering webs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8111—Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4282—Addition polymers
- D04H1/4291—Olefin series
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- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47K—SANITARY EQUIPMENT NOT OTHERWISE PROVIDED FOR; TOILET ACCESSORIES
- A47K10/00—Body-drying implements; Toilet paper; Holders therefor
- A47K10/24—Towel dispensers, e.g. for piled-up or folded textile towels; Toilet-paper dispensers; Dispensers for piled-up or folded textile towels provided or not with devices for taking-up soiled towels as far as not mechanically driven
- A47K10/32—Dispensers for paper towels or toilet-paper
- A47K2010/3266—Wet wipes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
Definitions
- the present invention relates to multi-ply wipes.
- the invention particularly concerns 5 wet wipes which include a multi-ply basesheet.
- wet wipes are well known and have been produced in many forms.
- One of the most common forms of wet wipes is a stack of moistened sheets packaged in a plastic container.
- Wet wipes have been made from a variety of materials and have been o moistened with a variety of suitable wiping solutions. Such wet wipes have been used for baby wipes, hand wipes, household cleaning wipes, industrial wipes and the like.
- conventional wet wipes have included a single layer of a substantially homogeneous material.
- such conventional wet wipes have been formed by an air laid web of fibers which are uniformly mixed or distributed throughout the web.
- Wipes have been formed by a variety of polymeric, synthetic and natural fibers such as polyester, polyethylene, polypropylene and cellulosic fibers.
- Other conventional wet wipes have included a coformed web of polypropylene and cellulosic fibers wherein the fibers are uniformly mixed throughout the web.
- the present inventors have recognized the difficulties and problems of the prior art and in response thereto have developed a multi-ply wet wipe basesheet with improved 0 physical properties by including an additive in either the polypropylene or polyethylene fibers used to form one of the plys or layers of the wet wipe basesheet.
- the use of such an additive in a layered basesheet allows the physical properties of the basesheet to be modified to suit the intended purpose of the wipe.
- the layers of a wet wipe basesheet according to the present invention may be combined to provide a soft and flexible wipe while still maintaining the strength, integrity and resiliency of the wipe.
- the present invention provides a layered basesheet for a wet wipe having a polypropylene and a polyethylene layer in mutual contact.
- two outer polyethylene layers are bonded to an inner polypropylene layer.
- An additive is present in either the polypropylene or polyethylene fibers and thereby modifies one or more of the physical properties of the fibers and resulting wipe. Natural fibers may also be included in one, several, or all of the basesheet layers.
- an additive which lowers the melting temperature of polyethylene and which functions as a tackifier is added to the polyethylene fibers.
- a fully hydrogenated hydrocarbon resin additive may be used as a tackifier and to lower the melting temperature of linear low density polyethylene by more than 40 degrees from about 130 degrees Celsius to about 87 degrees Celsius.
- an additive for example a polybutylene such as a polybutene-1 copolymer, is present in the polypropylene fibers to increase the ply attachment or flexibility of the polypropylene layer.
- Another additive which may be used with the polypropylene fibers to increase their tackiness is polyethylene acrylic acid.
- the polyethylene fiber layer may also include natural fibers while the other fibrous layer may include natural fibers, synthetic fibers or both natural and synthetic fibers.
- Embodiments of the present invention may take the form of a nonwoven layered wet wipe basesheet which includes a first layer including polypropylene fibers and which has oppositely disposed first and second major surfaces; a second layer which includes polyethylene fibers and has an inward facing major surface and an oppositely disposed outward facing major surface wherein the inward facing surface is oriented towards and contacting the first major surface of the first layer and the outward facing surface of the second layer defines an exterior surface of the basesheet; and an additive which is present in either the polypropylene fibers or the polyethylene fibers.
- Embodiments of the present invention may also take the form of a nonwoven layered wet wipe basesheet which includes an inner layer including polypropylene fibers and having oppositely disposed first and second major surfaces; first and second outer layers each of which include polyethylene fibers and have an inward facing major surface and an oppositely disposed outward facing major surface, the inward facing major surfaces of the first and second outer layers being in respective contact with the first and second major surfaces of the inner layer, the outward facing major surfaces of the first and second outer layers defining two oppositely disposed major exterior surfaces of the basesheet; and an additive which is present in either the polypropylene fibers of the inner layer or the polyethylene fibers of the first and second outer layers.
- Additional embodiments of the present invention may take the form of a wet wipe having a nonwoven basesheet which includes a fibrous first layer and a second layer; the fibrous first layer has oppositely disposed first and second major surfaces; the second layer including a plurality of fibers and has an inward facing major surface and an oppositely disposed outward facing major surface, the inward facing major surface being oriented towards and contacting the first major surface of the first layer and the outward facing major surface defining an exterior surface of the basesheet and wherein the fibers of the second layer include fibers formed by a blend of polyethylene and an additive; and a solution disposed in the basesheet.
- Still further embodiments of the present invention may take the form of a wet wipe having a nonwoven basesheet which includes a first layer and a fibrous second layer; the first layer including a plurality of fibers and having oppositely disposed first and second major surfaces and wherein the fibers of the first layer include fibers formed by a blend of polypropylene and an additive; the fibrous second layer having an inward facing major surface and oppositely disposed outward facing major surface, the inward facing surface being oriented towards and contacting the first major surface and the outward facing major surface defining an exterior surface of the basesheet; and a solution disposed in the basesheet.
- the present invention in its various embodiments, provides several advantages. It allows different materials, including either polyethylene or polypropylene, to be combined to form a wet wipe basesheet in a manner which takes advantage of the different physical properties of the different materials.
- the layers of the basesheet may be combined to take advantage of the relative strength provided by polypropylene fibers, the relative softness provided by polyethylene fibers, or both of these properties.
- the use of an additive with either the polyethylene or the polypropylene fibers allows the properties of the basesheet to be further controlled to better adapt the basesheet properties to the intended purpose of the wipe.
- the present invention relates to multi-ply or layered basesheets for wet wipes.
- Basesheets in accordance with the present invention may be used to form baby wipes, hand and face wipes, cosmetic wipes, household wipes, industrial wipes and other wet - wipe products.
- Wet wipe basesheet layers can be made from a variety of materials including meltblown materials, coform materials, air-laid materials, bonded-carded web materials, hydroentangled materials, spunbond materials and the like, and can comprise synthetic or natural fibers.
- the layered basesheet may include a relatively soft layer which may include relatively soft and/or pliant synthetic fibers such as linear low density polyethylene fibers.
- the layered basesheet may also include a relatively strong, resilient layer which may include relatively resilient and high tensile strength synthetic fibers such as isotactic polypropylene fibers.
- the basesheets of the present invention are multi-ply basesheets which include at least two fibrous layers wherein one of the layers includes either polypropylene fibers or polyethylene fibers.
- the present invention may also advantageously combine two fibrous layers wherein a first layer includes polypropylene fibers and a second layer includes polyethylene fibers. Additional fibrous layers which do not include polyethylene or polypropylene fibers may also be utilized in the basesheets.
- a basesheet which includes both a polypropylene and polyethylene layer can take advantage of the different properties of both fibers.
- Polyethylene fibers are generally more pliant and therefore softer than polypropylene fibers. This is due to the inherent differences between polyethylene and polypropylene in viscosity, structural chemistry and fiber solidification.
- a basesheet produced with polyethylene fibers will, accordingly, generally be softer than a similar basesheet produced with polypropylene fibers.
- a basesheet produced with polypropylene will generally outperform a polyethylene basesheet in these latter properties but will not have the softness provided by a polyethylene basesheet.
- Basesheets are generally planar with two oppositely disposed major exterior surfaces.
- the side edges of the basesheet are of limited surface area and are generally not employed as wiping or cleaning surfaces by the end user of the wipe.
- the polyethylene layer can be used to define one or both major exterior surfaces of the basesheet.
- a polyethylene layer may define one major exterior surface of the basesheet while in a three ply basesheet, polyethylene layers may be used to define both of the major exterior surfaces of the basesheet.
- a polypropylene layer may be combined with a layer having greater softness to provide enhanced strength to the basesheet.
- a polyethylene layer or ply refers to a basesheet layer which includes polyethylene or polyethylene blend fibers.
- the polyethylene fibers may be homopolymer fibers or bi-component fibers.
- the polyethylene layer may also include non- polyethylene fibers such as natural fibers.
- a polypropylene layer includes polypropylene or polypropylene blend fibers.
- the polypropylene fibers may be homopolymer or bi-component fibers.
- the polypropylene layer may also include non- polypropylene fibers such as natural fibers.
- Additives may be blended into the polyethylene or polypropylene used to form the fibers.
- the presence of an additive in the polyethylene or polypropylene fibers may affect the properties of the polyethylene or polypropylene layer and provides another means by which the basesheet properties may be modified to adapt the basesheet for a particular use.
- a polyethylene and polypropylene layer may be combined together to form a two ply basesheet.
- the polypropylene first layer has oppositely disposed first and second major surfaces.
- the polyethylene second layer has an inward facing major surface and an outward facing major surface.
- the inward facing major surface of the polyethylene layer contacts the first major surface of the polypropylene layer.
- the outward facing major surface of the polyethylene layer defines an exterior surface of the basesheet and provides a relatively soft wiping surface while the polypropylene layer enhances the strength of the basesheet.
- Either, or both, of the polyethylene and polypropylene layers may also include natural fibers.
- the polypropylene layer may be a coformed layer of meltblown polypropylene microfibers and wood pulp fibers wherein the pulp to polymer weight ratio is from about 50/50 to about 75/25 and, advantageously, about 65/35.
- a suitable polypropylene is an isotactic polypropylene obtained from Montell USA Inc. of Wilmington, Delaware under the trade designation MONTELL PF015.
- the polyethylene layer may be a coformed layer of meltblown linear low density polyethylene microfibers and wood pulp fibers wherein the pulp to polymer weight ratio is from about 25/75 to about 75/25 and, advantageously, about either 50/50 or 65/35.
- a suitable polyethylene is available from Dow Chemical Co. under the tradename ASPUN 6831 A. Additional embodiments of the present invention may include additional fibrous plys.
- a three ply basesheet may advantageously include an inner polypropylene layer and two outer polyethylene layers.
- the outward facing surfaces of the two polyethylene layers may define both of the oppositely disposed major exterior surfaces of the basesheet.
- the inward facing major surfaces of the polyethylene layers are disposed in contact with the two major surfaces of the polypropylene layer whereby the polypropylene layer may provide strength to the basesheet without having a negative impact on the softness of the major exterior surfaces of the basesheet.
- Natural fibers may also be included in one or more of the layers of such a basesheet.
- Polyethylene and polypropylene fibers are thermally incompatible and generally do not bond well to each other.
- the polyethylene and polypropylene fibers may entangle with each other resulting in suitable securement between the layers.
- the polyethylene and polypropylene fibers may entangle with each other and the cellulosic fibers and may at least partially bond to the cellulosic fibers which results in securement between the layers.
- Such interlayer bonding and entanglement may be enhanced by a thermo-mechanical process wherein the layered basesheet is passed between a heated smooth anvil roll and a heated pattern roll.
- incorporation of an additive in either the polyethylene or polypropylene fibers can also improve the level of attachment between adjacent polyethylene and polypropylene layers.
- the use of a tackifier as the additive may provide such results.
- Tackifiers are known in the art and may be used to improve the adhesive or bonding properties of fibers in which they are incorporated. Tackifiers may be effectively added to materials with which the tackifer has a limited compatibility. Tackifiers often have molecular weights which have a broad distribution and fall within the range of 500-
- the softening points of such tackifiers may vary from 50 to 150 degrees Celsius.
- Tackifiers can improve the adhesion of an elastomeric material by reducing the material's resistance to deformation at low rates of deformation (thereby facilitating bond formation upon contact) while increasing the resistance to deformation at higher rates of deformation (thereby providing a stronger resistance to detachment).
- the tackifier may enable the adhesive mass to contact the surface more intimately, thus enhancing bond strength.
- This functionality of tackifiers is well-known and can be quantified or verified for a particular elastomeric material and tackifier by comparing the shear storage modulus of the elastomeric material with and without the tackifier.
- a polyethylene blend containing 80% polyethylene and 20% REGALREZ 1126® produces fibers having a melting temperature of approximately 87 degrees Celsius. This compares to a melting temperature of approximately 130 degrees Celsius for the virgin polyethylene used to form the blend.
- the "tackifying" attributes of the REGELREZ® 1 126 are considered to be primarily responsible for any increase in the number of fiber to fiber bonds, it is also thought that the reduction in the melting temperature of the resultant polyethylene blend may have a potentially beneficial and incremental effect on the number of such bonds.
- the increased fiber to fiber bonding among the polyethylene fibers is also thought to improve ply attachment.
- the individual polyethylene fibers which do bond to, or become entangled with, fibers in the adjacent layer are likely to be more strongly secured to other fibers within the polyethylene layer when there are more fiber to fiber bonds between polyethylene fibers and thus provide a relatively stronger attachment between layers.
- Basesheet layers containing (by weight) 65% cellulosic pulp and 35% polyethylene fibers formed with a blend containing 80% polyethylene and 20% REGALREZ 1126® may be perceived by some individuals to be less soft than a layer formed with 65% cellulosic pulp and 35% virgin polyethylene. It is thought that the increased number of polyethylene fiber bonds may reduce the pliancy of the polyethylene fibers and thereby affect the tactile properties of the fibers in a manner which is perceptible for some individuals. It has also been found that the use of an additive with polypropylene fibers can improve the level of attachment between adjacent layers of polypropylene and polyethylene.
- polybutylene as an additive can increase the tackiness of the polypropylene fibers, and, at levels of 20% and 50%, was found to have a positive effect on ply attachment.
- the use of polybutylene as an additive was also found to be capable of reducing the stiffness of the basesheet.
- a reduction in the stiffness, i.e., an increase in the flexibility, of the basesheet generally has a positive influence on the tactile perception of the basesheet.
- an increase in flexibility can occur in an inner ply which does not form one of the major exterior surfaces of the basesheet and still produce this positive influence on the tactile perception of the basesheet.
- Polyethylene acrylic acid is another additive which may be incorporated into the polypropylene fibers, either by itself or in combination with polybutylene, to enhance the tackiness of the polypropylene fibers.
- the blending of a polyethylene acrylic acid with polypropylene is described in U.S. Pat. No. 4,797,318 which is incorporated herein by reference.
- a basesheet having a polyethylene layer and at least one additional fibrous layer is provided.
- the fibers of the polyethylene layer include polyethylene fibers formed with a blend containing both polyethylene and an additive.
- the polyethylene layer may also include natural fibers.
- the fibers of the additional fibrous layer may be either synthetic, natural or a mixture of synthetic and natural fibers.
- a basesheet having a polypropylene layer and at least one additional fibrous layer is provided.
- the fibers of the polypropylene layer include polypropylene fibers formed with a blend containing both polypropylene and an additive.
- the polypropylene layer may also include natural fibers.
- the fibers of the additional fibrous layer may be either synthetic, natural or a mixture of synthetic and natural fibers.
- Natural fibers such as cellulosic fibers may be used in the wet wipe basesheet to provide enhanced thickness and wettability.
- the natural fibers may also provide void volume within the basesheet which may increase the moisture capacity of the basesheet.
- Examples of natural fibers suitable for use in the present invention include not only cellulosic fibers such as wood pulp fibers, but also cotton fibers, flax fibers, jute fibers, silk fibers and the like.
- examples of thermoplastic polymeric fibers suitable for use with the present invention include polyamides, and polyesters such as polyethylene terephthalate.
- Alternative synthetic fibers which may be suitable include staple nylon and rayon fibers.
- a layer of the multi-ply basesheet is a combination of synthetic and natural fibers, such as polypropylene and cellulosic fibers
- the relative percentages of the synthetic fibers and natural fibers in the layer can vary over a wide range depending on the desired characteristics of the wet wipes.
- the layer may comprise from about 20 to about 95 weight percent, desirably from about 20 to about 60 weight percent, and more desirably from about 30 to about 40 weight percent of synthetic fibers based on the dry weight of the layer.
- Such a layer of synthetic and natural fibers may be manufactured by methods well known to those skilled in the art.
- a layer containing both synthetic and natural fibers be formed by a coform process which provides a generally uniform distribution of the synthetic and natural fibers within the individual layer.
- the manufacture of coform layers is described in U.S. Patent No. 4,100,324 to Anderson et al. which issued July 11 , 1978; U.S. Patent No. 4,604,313 to McFarland et al. which issued August 5, 1986; and U.S. Patent No. 5,350,624 which issued September 27, 1994; the disclosures of which are herein incorporated by reference.
- coform layers comprise a matrix of thermoplastic polymeric meltblown microfibers, such as polypropylene microfibers, and cellulosic fibers, such as wood pulp fibers.
- a coform layer is formed by initially forming at least one primary air stream containing the synthetic fibers and merging the primary stream with at least one secondary stream of natural fibers.
- the primary and secondary streams are merged under turbulent conditions to form an integrated stream containing a homogeneous distribution of the fibers.
- the integrated air stream is directed onto a forming surface to air form a layer of material.
- a multiplicity of these coform layers can be formed in succession to provide a web of multiple coform layers.
- the attachment of polyethylene and polypropylene coform layers may be enhanced by a thermo-mechanical process wherein the layered basesheet is passed between a heated smooth anvil roll and a heated pattern roll.
- the pattern roll may have any raised pattern which provides the desired entanglement and interlayer bonding. Desirably, the pattern roll defines a raised pattern which defines a plurality of bond locations which define a bond area of between about 4 and about 30 percent of the total area of the roll.
- the pressure between the rolls and the temperature of the rolls must be balanced to produce a basesheet having adequate strength and integrity while maintaining the softness of the outer layers.
- the temperature and pressure may vary depending upon the types of fibers being used to provide the desired wet wipe.
- the pressure between the rolls may be between about 50 and about 900 newtons per lineal centimeter and the temperature of at least one of the rolls may be between about 40 and about 150 degrees Celsius for improved entanglement and bonding. Under such conditions of temperature and pressure, the polyethylene fibers deform to provide mechanical entanglement with and possible bonding to the polypropylene fibers.
- the multi-ply basesheet may have a total basis weight of from about 25 to about 120 grams per square meter and desirably from about 40 to about 90 grams per square meter.
- the basis weight of the basesheet may also vary depending upon the desired end use of the wet wipe.
- a suitable basesheet for wiping the skin may have a basis weight of from about 60 to about 80 grams per square meter and desirably about 75 grams per square meter.
- the layered basesheet may include coform layers of polypropylene and cellulosic fibers and polyethylene and cellulosic fibers and have a basis weight of from about 60 to about 90 grams per square meter and desirably about 80 grams per square meter.
- Each layer of the basesheet may or may not have the same basis weight depending upon the desired properties of the wet wipe.
- the basis weight of the layers may define an outer/inner/outer layer weight ratio of from about 10/80/10 to about 40/20/40, desirably about 25/50/25 to about 33/33/33 and more desirably about 30/40/30 based on a total weight of the basesheet.
- the basesheet should have sufficient strength to withstand the forces exerted by the user when it is wetted with solution.
- the layer which includes polypropylene fibers will generally provide the majority of the basesheet strength while the polyethylene fibers may be used to provide a soft exterior surface for the wet wipe.
- the tensile strength of such a layered basesheet may be higher than the tensile strength of a single layer containing polyethylene fibers and provide softer exterior surfaces than a single layer containing polypropylene fibers.
- Multi-ply basesheets in accordance with the present may be manufactured on a single manufacturing line which includes multiple individual forming banks.
- Each forming bank is configured to provide an individual ply or layer.
- the first and last forming banks may be configured to provide the outer layers while the middle or interior forming banks may be configured to provide one or more inner layers.
- the mechanical entanglement of fibers in adjacent layers during the forming process attaches the adjacent layers. Bonds may also form between fibers of adjacent layers to provide further attachment of the adjacent layers of the basesheet. Subsequent thermomechanical bonding may also be used to improve the attachment between the adjacent layers.
- Each forming bank will include the appropriate equipment to provide the desired type of web.
- each layer comprises a coform layer of meltblown microfibers and natural fibers such as wood pulp fibers
- each forming bank may include a plurality of meltblowing dies to extrude a molten polymeric material in fine streams. The fine streams are then attenuated by converging flows of high velocity gas to break the polymer streams into discrete microfibers of small diameter.
- meltblowing dies are well known to those skilled in the art.
- the stream or streams of natural fibers which are converged with the streams of meltblown microfibers may be provided by a conventional pulp picker roll process as is well known to those skilled in the art.
- one or more layers of the wet wipe basesheet can be made from a different type of material such as a meltblown sheet of polymeric microfibers.
- a meltblown sheet of polymeric microfibers For example, an inner, strong and resilient layer may be formed with a layer of meltblown polypropylene fibers while soft outer layers may be formed with coform layers of polyethylene and wood pulp fibers as described above. Soft and flexible outer layers may also be provided by different types of materials such as airlaid, carded web, or meltblown materials which are manufactured by processes well known to those skilled in the art.
- the basesheet of the present invention is used to form a wet wipe by adding an appropriate solution to the basesheet.
- the solution may be any liquid which can be absorbed into the wet wipe basesheet and may include a variety of different components which provide the desired wiping properties.
- the components may include water, emollients, surfactants, fragrances, preservatives, chelating agents, pH buffers or combinations thereof as are well known to those skilled in the art.
- the solution may also contain lotions and/or medicaments.
- the amount of solution contained within each wet wipe may vary depending upon the type of material forming the basesheet, the type of solution being used, the type of container being used to store the wet wipes, and the intended use of the wet wipe. Generally, each wet wipe will contain from about 150 to about 600 weight percent and desirably from about 250 to about 450 weight percent solution based on the dry weight of the basesheet. It is generally desirable that the amount of solution contained within the wet wipe be from about 300 to about 400 weight percent and, advantageously, about 330 weight percent based on the dry weight of the basesheet.
- the resulting wet wipe may be too dry and may not adequately perform. If excessive solution is added to the basesheet, the resulting wet wipe may be oversaturated and soggy and the solution may pool in the bottom of the container.
- Basesheets, and resulting wet wipes are generally rectangular in shape and may have any suitable unfolded width and length.
- the wet wipe may have an unfolded length of from about 2.0 to about 80.0 centimeters and desirably from about 10.0 to about 25.0 centimeters and an unfolded width of from about 2.0 to about 80.0 centimeters and desirably from about 10.0 to about 25.0 centimeters.
- individual wet wipes are arranged in a folded configuration and stacked one on top of the other to provide a stack of wet wipes.
- Such folded configurations are well known to those skilled in the art and include c-folded, z-folded, quarter-folded and similar configurations.
- a stack of folded wet wipes may be placed in the interior of a container, such as a plastic tub, to provide a package of wet wipes for eventual sale to the consumer. If the stack is interfolded, the wipes may be conveniently dispensed using what is commonly referred to as a "pop-up" dispenser.
- the wet wipe basesheets may form a continuous strip of material which has perforations between each individual wipe. A continuous strip of basesheet material may be arranged in a stack or wound into a roll for dispensing.
- a matrix of additives and fibrous layers was developed to compare the efficacy and properties of different additives. Separate samples according to each code were prepared and compared. Each of the samples was a two-layer material having a polyethylene coform layer and a polypropylene coform layer. To facilitate comparison of the different samples, each of the basesheet samples had a target basis weight of 54 grams per square meter (gsm) and each sample layer included 65% cellulosic pulp by weight. The different samples are listed in the following table:
- PE polyethylene
- PP polypropylene
- the hydrocarbon resin added to the polyethylene of codes 2, 3 and 7 was REGALREZ 1 126® which is a fully hydrogenated hydrocarbon resin produced by Hercules Inc. having offices in Wilmington, Delaware. This resin is produced by polymerization and hydrogenation of pure monomer hydrocarbon feedstocks and is a highly stable, light-colored, low molecular weight, nonpoiar resin.
- the hydrocarbon resin pellets were relatively "sticky." To improve processing, the hydrocarbon resin pellets were compounded into the polyethylene and the resulting blend was re-pelletized in a twin screw extrusion process. The blended pellets were then used to form the polyethylene fibers.
- the polyethylene and hyrdocarbon ply was formed in a process wherein the extrusion temperature was 243°C (470°F), the air temperature of the primary air stream conveying the polyethylene fibers was 277-282°C (530-540°F); and the forming height was 25.4-27.9 cm (10-11 inches).
- the extrusion temperature was 249°C (480°F)
- the air temperature of the primary air stream conveying the polyethylene fibers was 277-282°C (530-540°F)
- the forming height was 25.4-30.5 cm (10-12 inches).
- the polybutylene was obtained under the tradename Shell DP 8911 from Shell Chemical Co. having offices in Houston, Texas and has since become available under the tradename DURAFLEX 8911 from Montell USA Inc.
- the atactic polypropylene was obtained under the tradename REXTAC-2115 from Huntsman, Inc. having offices in Houston and Odessa, Texas.
- the polypropylene and polybutylene ply was formed in a process wherein the extrusion temperature was 243°C (470°F), the air temperature of the primary air stream conveying the polypropylene fibers was 268-288°C (515-550°F), and the forming height was 25.4-30.5 cm (10-12 inches).
- the extrusion temperature was 260°C (500°F)
- the air temperature of the primary air stream conveying the polypropylene fibers was 288°C (550°F)
- the forming height was 27.9 cm (11 inches).
- the polyethylene was a linear low density polyethylene and was obtained under the tradename ASPUN 6831 from Dow Chemical having offices in Midland, Michigan.
- the polypropylene was obtained under the tradename Montell PF015 from Montell USA Inc. having offices in Wilmington, Delaware.
- Code 1 did not include an additive in either the polyethylene fibers or the polypropylene fibers and was used as a control. Two versions of code 1 were produced; a "PE control” in which a polyethylene coform layer was formed on a polypropylene coform layer already present on the web former; and a "PP control” in which a polypropylene coform layer was formed on a polyethylene coform layer already present on the web former.
- Codes 2 and 3 were formed in the same fashion as the PE control, i.e., the polyethylene coform layer was formed onto the polypropylene coform layer. Thus, the effectiveness of the additives used in Codes 2 and 3 is most directly determinable by a comparison to the PE control.
- Codes 4-6 were formed in the same fashion as the PP control, i.e., the polypropylene coform layer was formed onto the polyethylene coform layer. Thus, the effectiveness of the additives used in Codes 4-6 is most directly determinable by a comparison to the PP control.
- the peel strength, linting, cup crush and tensile strength (in both the machine direction "MD" and cross machine direction "CD") of the samples was tested to provide a relative comparison of the different samples for these physical parameters.
- the samples Prior to peel testing, the samples were each bonded with a similar pattern.
- the bonding pattern bonded approximately 13% of the surface area of the sample.
- the bonding was conducted at a pressure of about 131.3 Newtons per lineal centimeter (75 pounds per linear inch).
- the average hot oil core temperature of the bonder was approximately 77°C (170°F), and the bonding temperature was estimated to be approximately 68 to 71 °C (155 to 160° F).
- the peel test samples were prepared by first cutting a 7 inch by 7 inch section of wipe and adding solution to the wipe whereby the wipe contains solution in the amount of 330% of the dry weight of the wipe.
- the solution is the same solution as is used with Huggies® Wet Wipes which are commercially produced by Kimberly-Clark Corp. having offices in Neenah, WI (deionized water may be used as an alternative solution).
- a 2 ⁇ 0.04 inch (13 ⁇ 1 mm) by 7 ⁇ 0.04 inch (152 ⁇ 1 mm) sample is then cut from the saturated wipe with the longer side running parallel to the machine direction. The edges on the sample must be clean cut and parallel.
- a Constant Rate of Extension unit (or tensile tester) equipped with an appropriate load cell and computerized data acquisition system is used to perform the peel strength test.
- Appropriate tensile testers and load cells may be obtained from Instron Corp. of Canton, MA or Sintech, Inc. of Research Triangle Park, NO
- the grips of the tensile tester are installed parallel to each other.
- the tensile tester settings are as follows: the crosshead speed is set at 20 ⁇ 0.04 inch/min (508 ⁇ 10 mm/min); the gage length is set at 1.0 ⁇ 0.04 inch (25 ⁇ 1 mm); the Start Measurement is set at 0.5 ⁇ 0.04 inch (13 ⁇ 1 mm); and the End Measurement is set at 6 ⁇ 0.04 inch (152 ⁇ 1 mm).
- the test is conducted by first manually separating the polyethylene and polypropylene layers at one end of the sample. The plys are separated for a length of approximately 1 inch and no more than 2 inches. The two layers are then placed in opposite grips of a testing device so that the sample is straight and without slack. The testing device is then used to pull apart the layers (whereby the separated layers form a 180° angle) at the specified rate while simultaneously recording the force necessary to separate the layers in grams of force.
- a modified Gelbo unit was used for the measurement of sheet linting.
- a suitable testing unit may be obtained from US Testing Co., Inc., PO Box 3189, 1415 Park Avenue, Hoboken, NJ 07030. This test is used to determine the relative quantity of particles released from a fabric when it is subjected to a continuous flexing and twisting movement.
- At least five basesheets are used for any sample determination. At least seven basesheets should be initially collected, reserving the top and bottom basessheets for specimen protection only.
- the test specimens should be clean, dry, and free from environmental contamination.
- the test specimens should also be free of folds, wrinkles, and any other distortion which would constitute an abnormality. Performing the test on six to ten specimens is typically sufficient to provide a reasonable degree of confidence for obtaining an average sample value. Outlying values may be excluded when computing the average sample value.
- a dry 9" x 9" (23 cm by 23 cm) basesheet is placed in the modified Gelbo flexing unit where the sheet is strapped between two discs which hold the sheet in a tubular configuration.
- the sheet is carefully mounted, and with minimal handling, while the flexing heads are extended to their maximum distance.
- the specimen should have a gap at the top position of the tube formed by the sheet and the machine direction of the sheet should correspond to the long axis of the tube.
- the sheet is then turned and flexed to emit lint for a period of five minutes.
- the two holders have a flexing stroke of 4.7 in. (119.8 mm) and there is a twist to the shaft of 180° and a stroke rate of about 60 cycles per minute.
- the sheet is removed and the amount of emitted lint is determined. Due to the amount of lint produced, the measurement of the lint is performed by measuring the basis weight of the sheet before and after flexing the sheet rather than using a particle counter.
- the test equipment should be located in, and the samples conditioned to, a common testing atmosphere.
- the testing atmosphere should conform to either ASTM conditions (65 ⁇ 2% RH and 72 ⁇ 2° F) or TAPPI conditions (50 ⁇ 2% RH and 72 ⁇ 1.8° F).
- the total energy of a nonwoven fabric may be measured according to the "cup crush” test.
- the cup crush test evaluates fabric stiffness by measuring the peak load (also called the “cup crush") required for a 4.5 cm diameter hemispherically shaped foot to crush a 23 cm by 23 cm piece of fabric shaped into an approximately 6.5 cm diameter by 6.5 cm tall inverted cup while the cup shaped fabric is surrounded by an approximately 6.5 cm diameter cylinder to maintain a uniform deformation of the cup shaped fabric.
- An average of between 5 and 10 readings may be used to determine the final value, a smaller number of readings is appropriate when there is little or no variability in the individual readings while a larger number of readings is preferred when there is greater variability in the readings.
- the foot and the cup are aligned to avoid contact between the cup walls and the foot which could affect the readings. The foot descends at a rate of about 0.25 inches per second (380 mm per minute).
- the cup crush test yields a value for the total energy required to crush a sample (the "crush energy") which is the total energy from the start of the test to the peak load point.
- the total or crush energy is calculated by determining the area under the curve formed by the load in grams on one axis and the distance the foot travels in millimeters on the other from the start of the test to the peak load. The crush energy is, therefore, reported in gm-mm.
- cup crush values indicate a less stiff fabric which is generally also considered a softer fabric.
- a suitable device for measuring cup crush is a model TD-G-500 load cell (500 gram range) available from the Schaevitz Company, Pennsauken, N.J.
- the peak tensile strength of the samples was determined using a strip tensile test well known in the art.
- the samples are prepared by first cutting a 7 inch by 7 inch section of wipe and adding solution to the wipe whereby the wipe contains solution in the amount of 330% of the dry weight of the wipe.
- the solution is the same solution as is used with Huggies® Wet Wipes which are commercially produced by Kimberly-Clark Corp. having offices in Neenah, WI (deionized water may be used as an alternative solution).
- a 1 ⁇ 0.04 inch (25 ⁇ 1 mm) by 6 ⁇ 0.04 inch (150 ⁇ 1 mm) sample is then cut from the saturated wipe with the test direction (machine or cross direction) running parallel to the longer side of the strip. The edges on the sample must be clean cut and parallel.
- a Constant Rate of Extension unit (or tensile tester) equipped with an appropriate load cell and computerized data acquisition system is used to perform the test.
- Appropriate tensile testers and load cells may be obtained from Instron Corp. of Canton,
- the grips of the tensile tester are installed parallel to each other.
- the tensile tester settings are as follows: the crosshead speed is set at 12 ⁇ 0.04 inch/min (300 ⁇ 10 mm/min); the Chart is set at 12 ⁇ 0.04 inch/min (300 ⁇ 10 mm/min); the gage length (measured from the center of the upper horizontal line clamp to the center of the bottom horizontal line clamp) is set at 3.0 ⁇ 0.04 inch (76 ⁇ 1 mm); and the Fail (Break Criterion) is 65%.
- the test is conducted by placing the specimen symmetrically in the clamps with the longer dimension being parallel to the direction of the load application. The crosshead is then started and allowed to continue until the sample fails. The maximum load measured is recorded as the Peak Tensile Strength. The peak tensile energy and peak stretch may also be determined using the data from this test.
- the peak tensile strength of the tested codes was determined in both the machine direction (MD) and cross-machine direction (CD) of the material.
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020017008384A KR20010101335A (en) | 1998-12-31 | 1999-12-29 | Multi-Ply Wipe |
BR9916687-9A BR9916687A (en) | 1998-12-31 | 1999-12-29 | Wet wipes that include a multilayer base sheet |
JP2000590522A JP2003535982A (en) | 1998-12-31 | 1999-12-29 | Multi-layer wipe |
CA002355311A CA2355311A1 (en) | 1998-12-31 | 1999-12-29 | Multi-ply wipe |
AU22223/00A AU748707B2 (en) | 1998-12-31 | 1999-12-29 | Multi-ply wipe |
EP99966734A EP1156738A1 (en) | 1998-12-31 | 1999-12-29 | Multi-ply wipe |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11440998P | 1998-12-31 | 1998-12-31 | |
US60/114,409 | 1998-12-31 | ||
US32943699A | 1999-06-10 | 1999-06-10 | |
US09/329,436 | 1999-06-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000038565A1 true WO2000038565A1 (en) | 2000-07-06 |
Family
ID=26812153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1999/031289 WO2000038565A1 (en) | 1998-12-31 | 1999-12-29 | Multi-ply wipe |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1156738A1 (en) |
JP (1) | JP2003535982A (en) |
KR (1) | KR20010101335A (en) |
AR (1) | AR022164A1 (en) |
AU (1) | AU748707B2 (en) |
BR (1) | BR9916687A (en) |
CA (1) | CA2355311A1 (en) |
CO (1) | CO5111032A1 (en) |
TW (1) | TW529924B (en) |
WO (1) | WO2000038565A1 (en) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002053365A3 (en) * | 2000-12-29 | 2003-03-06 | Kimberly Clark Co | Composite material with cloth-like feel |
WO2004067825A1 (en) * | 2003-01-20 | 2004-08-12 | Kinsei Seishi Co., Ltd. | Dry-process nonwoven pulp fabric composed of united layer structures |
WO2009070575A1 (en) * | 2007-11-28 | 2009-06-04 | Babcock & Wilcox Technical Services Y-12, Llc | Cleaning medium for removing contamination and method of making |
WO2010017189A1 (en) * | 2008-08-04 | 2010-02-11 | The Procter & Gamble Company | Multi-ply fibrous structures and processes for making same |
WO2011123584A1 (en) * | 2010-03-31 | 2011-10-06 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US8753737B2 (en) | 2009-05-19 | 2014-06-17 | The Procter & Gamble Company | Multi-ply fibrous structures and methods for making same |
US8852474B2 (en) | 2007-07-17 | 2014-10-07 | The Procter & Gamble Company | Process for making fibrous structures |
US8906816B2 (en) | 2007-09-03 | 2014-12-09 | Sca Hygiene Products Ab | Laminate having improved wiping properties and a method for producing the laminate |
US8921244B2 (en) | 2005-08-22 | 2014-12-30 | The Procter & Gamble Company | Hydroxyl polymer fiber fibrous structures and processes for making same |
US9243368B2 (en) | 2009-05-19 | 2016-01-26 | The Procter & Gamble Company | Embossed fibrous structures and methods for making same |
US9458573B2 (en) | 2009-11-02 | 2016-10-04 | The Procter & Gamble Company | Fibrous structures and methods for making same |
WO2018017597A1 (en) * | 2016-07-18 | 2018-01-25 | Naturezway, Inc. | Compostable and biodegradable wet wipe pad for cleaning mop heads |
US10024000B2 (en) | 2007-07-17 | 2018-07-17 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US10463222B2 (en) | 2013-11-27 | 2019-11-05 | Kimberly-Clark Worldwide, Inc. | Nonwoven tack cloth for wipe applications |
US10858785B2 (en) | 2007-07-17 | 2020-12-08 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US10895022B2 (en) | 2009-11-02 | 2021-01-19 | The Procter & Gamble Company | Fibrous elements and fibrous structures employing same |
US11414798B2 (en) | 2007-07-17 | 2022-08-16 | The Procter & Gamble Company | Fibrous structures |
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- 1999-12-28 CO CO99081144A patent/CO5111032A1/en unknown
- 1999-12-29 CA CA002355311A patent/CA2355311A1/en not_active Abandoned
- 1999-12-29 JP JP2000590522A patent/JP2003535982A/en active Pending
- 1999-12-29 WO PCT/US1999/031289 patent/WO2000038565A1/en not_active Application Discontinuation
- 1999-12-29 BR BR9916687-9A patent/BR9916687A/en active Search and Examination
- 1999-12-29 AU AU22223/00A patent/AU748707B2/en not_active Ceased
- 1999-12-29 AR ARP990106853A patent/AR022164A1/en unknown
- 1999-12-29 EP EP99966734A patent/EP1156738A1/en not_active Withdrawn
- 1999-12-29 KR KR1020017008384A patent/KR20010101335A/en not_active Application Discontinuation
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- 2000-03-01 TW TW088123268A patent/TW529924B/en active
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Cited By (29)
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KR100805561B1 (en) * | 2000-12-29 | 2008-02-20 | 킴벌리-클라크 월드와이드, 인크. | Composite Material with Cloth-like Feel |
WO2002053365A3 (en) * | 2000-12-29 | 2003-03-06 | Kimberly Clark Co | Composite material with cloth-like feel |
US6811638B2 (en) | 2000-12-29 | 2004-11-02 | Kimberly-Clark Worldwide, Inc. | Method for controlling retraction of composite materials |
KR101049623B1 (en) * | 2003-01-20 | 2011-07-14 | 긴세이 세이시 가부시키가이샤 | Dry pulp nonwoven fabric with integrated layer structure |
WO2004067825A1 (en) * | 2003-01-20 | 2004-08-12 | Kinsei Seishi Co., Ltd. | Dry-process nonwoven pulp fabric composed of united layer structures |
US8921244B2 (en) | 2005-08-22 | 2014-12-30 | The Procter & Gamble Company | Hydroxyl polymer fiber fibrous structures and processes for making same |
US11414798B2 (en) | 2007-07-17 | 2022-08-16 | The Procter & Gamble Company | Fibrous structures |
US10858785B2 (en) | 2007-07-17 | 2020-12-08 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US10024000B2 (en) | 2007-07-17 | 2018-07-17 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US9926648B2 (en) | 2007-07-17 | 2018-03-27 | The Procter & Gamble Company | Process for making fibrous structures |
US8852474B2 (en) | 2007-07-17 | 2014-10-07 | The Procter & Gamble Company | Process for making fibrous structures |
US8906816B2 (en) | 2007-09-03 | 2014-12-09 | Sca Hygiene Products Ab | Laminate having improved wiping properties and a method for producing the laminate |
WO2009070575A1 (en) * | 2007-11-28 | 2009-06-04 | Babcock & Wilcox Technical Services Y-12, Llc | Cleaning medium for removing contamination and method of making |
WO2010017189A1 (en) * | 2008-08-04 | 2010-02-11 | The Procter & Gamble Company | Multi-ply fibrous structures and processes for making same |
US9937694B2 (en) | 2009-05-19 | 2018-04-10 | The Procter & Gamble Company | Method for making multi-ply fibrous structures |
US9243368B2 (en) | 2009-05-19 | 2016-01-26 | The Procter & Gamble Company | Embossed fibrous structures and methods for making same |
US9701101B2 (en) | 2009-05-19 | 2017-07-11 | The Procter & Gamble Company | Multi-ply fibrous structures and methods for making same |
US8753737B2 (en) | 2009-05-19 | 2014-06-17 | The Procter & Gamble Company | Multi-ply fibrous structures and methods for making same |
US9458573B2 (en) | 2009-11-02 | 2016-10-04 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US11618977B2 (en) | 2009-11-02 | 2023-04-04 | The Procter & Gamble Company | Fibrous elements and fibrous structures employing same |
US10895022B2 (en) | 2009-11-02 | 2021-01-19 | The Procter & Gamble Company | Fibrous elements and fibrous structures employing same |
GB2493292B (en) * | 2010-03-31 | 2014-02-26 | Procter & Gamble | Fibrous structures |
GB2493292A (en) * | 2010-03-31 | 2013-01-30 | Procter & Gamble | Fibrous structures and methods for making same |
FR2959518A1 (en) * | 2010-03-31 | 2011-11-04 | Procter & Gamble | FIBROUS STRUCTURES AND METHODS OF PREPARATION |
WO2011123584A1 (en) * | 2010-03-31 | 2011-10-06 | The Procter & Gamble Company | Fibrous structures and methods for making same |
US9631321B2 (en) | 2010-03-31 | 2017-04-25 | The Procter & Gamble Company | Absorptive fibrous structures |
US11680373B2 (en) | 2010-03-31 | 2023-06-20 | The Procter & Gamble Company | Container for fibrous wipes |
US10463222B2 (en) | 2013-11-27 | 2019-11-05 | Kimberly-Clark Worldwide, Inc. | Nonwoven tack cloth for wipe applications |
WO2018017597A1 (en) * | 2016-07-18 | 2018-01-25 | Naturezway, Inc. | Compostable and biodegradable wet wipe pad for cleaning mop heads |
Also Published As
Publication number | Publication date |
---|---|
TW529924B (en) | 2003-05-01 |
AU748707B2 (en) | 2002-06-13 |
EP1156738A1 (en) | 2001-11-28 |
KR20010101335A (en) | 2001-11-14 |
AU2222300A (en) | 2000-07-31 |
JP2003535982A (en) | 2003-12-02 |
AR022164A1 (en) | 2002-09-04 |
CA2355311A1 (en) | 2000-07-06 |
CO5111032A1 (en) | 2001-12-26 |
BR9916687A (en) | 2001-10-30 |
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