MXPA06006057A - Disposable scrubbing product - Google Patents

Disposable scrubbing product

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Publication number
MXPA06006057A
MXPA06006057A MXPA/A/2006/006057A MXPA06006057A MXPA06006057A MX PA06006057 A MXPA06006057 A MX PA06006057A MX PA06006057 A MXPA06006057 A MX PA06006057A MX PA06006057 A MXPA06006057 A MX PA06006057A
Authority
MX
Mexico
Prior art keywords
abrasive
layer
fabric
fibers
product
Prior art date
Application number
MXPA/A/2006/006057A
Other languages
Spanish (es)
Inventor
Chen Fungjou
Dean Lindsay Jeffrey
Zhou Peiguang
G Druecke Frank
Bednarz Julie
Schrodt Ivan
Original Assignee
Kimberlyclark Worldwide Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kimberlyclark Worldwide Inc filed Critical Kimberlyclark Worldwide Inc
Publication of MXPA06006057A publication Critical patent/MXPA06006057A/en

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Abstract

The present invention discloses a disposable scrubbing product for use in household cleaning or personal care applications. The scrubbing product (330) of the invention is a multi-layer laminate product and generally includes at least two distinct layers (332), an abrasive layer (334) and an absorbent fibrous layer such as a layer tissue made from papermaking fibers, a layer of coform, an airlaid web, or combinations thereof. The abrasive layer is formed primarily of polymeric fibers in a disordered or random distribution as is typical of fibers deposited in meltblown or spunbond processes so as to form an open, porous structure. In one embodiment, multiple layers of an abrasive structure are releasably attached together. In this manner, the top or outermost layer may be removed after being used in order to expose an unused abrasive structure located below the discarded layer.

Description

DISPOSABLE PRODUCT TO SCRUB Background of the Invention Scouring pads are commonly used for many cleaning and personal care practices. In general, scouring pads include a natural or manufactured occurrence abrasive material. Examples of typical materials include pumice, loofah, metal fiber, and a wide variety of plastic materials, a nonabsorbent abrasive material is often combined with a backing material of the absorbent sponge type in these products. For example, the abrasive material often forms a layer on a multilayer product that also includes an absorbent layer of natural sponge, regenerated cellulose, or some other type of foamy absorbent product.
These scrubbing pads tend to be expensive, making them unsuitable for a single-use or disposable product. Due to the nature of the product's use, however, the products can become dirty with dirt, grease, bacteria, and other contaminants after only one or two uses. As a result, consumers should replace these expensive scrub pads frequently in order to feel safe knowing that they are using an uncontaminated cleaning pad.
Examples of abrasive cleaning articles have been described in the past. See, for example, the published international application number WO 02/41748, the United States of America patent number 5,213,588 and the United States of America patent number 6,013,349.
The present invention is directed to these and other problems encountered with scouring pads in the past and is directed to disposable scouring pads that can provide a wide variety of abrasion level, can be thin, comfortable and easy to hold, can have good absorbency, and can provide benefits not previously supplied in the abrasive cleaning articles of the past.
Synthesis of the Invention The present invention is directed to a disposable scouring product for use in household cleaning or in personal care applications, as well as in industrial cleaning and other applications.
The scouring product of the invention is a multi-layered product and generally includes at least two distinct layers, an abrasive layer and an absorbent fibrous layer such as a tissue layer made of papermaking fibers, a coform layer of a fabric placed by air, or combinations of the same or other known cellulose fabrics. The abrasive layer is formed mainly of rough polymeric fibers in a random or random distribution as is typical of the fibers deposited in the meltblown or spunbond processes.
The abrasive layer may comprise, for example, aggregated multi-filament fibers formed by the partial melting of a plurality of polymer strands (e.g., individual fibers produced by the process) during a meltblowing process or other forming process. of fiber to form an integral structure of the generally non-circular fiber type in which the substantially parallel polymeric filaments are joined along their sides. Such multi-filament aggregates can have a much larger effective diameter than the individual yarns normally obtained in meltblowing or spin-jointing processes, and a complex shape of a cross-section more suitable for providing abrasion than can be achieved with Conventional circular fibers, and can contribute to effective cleaning and abrasion.
In one embodiment of the present invention, a scrubbing product is constructed that contains a plurality of abrasive structures configured in a stacked array. Optionally, the plurality of abrasive structures can be coupled to the upper surface of an absorbent substrate to the liquid. The absorbent substrate to the liquid may have, for example, characteristics of the sponge type. For example, the liquid-absorbent structure can be made of a sponge or a sponge-type synthetic material. Alternatively, the liquid-absorbent substrate can be made from a plurality of layers stacked absorbent to the liquid. The liquid absorbent layers may comprise, for example, paper fabrics, coform fabrics, air laid fabrics, and the like.
In this embodiment, the scrubbing product further includes a coupling structure for releasably engaging the plurality of abrasive structures together. In particular, the coupling structure supports the plurality of abrasive structures together with sufficient force to allow the use of the scouring product without the plurality of delamination of the abrasive structures. The coupling structure, however, allows an abrasive upper structure to be removed from the product for scrubbing by a user when pulling or peeling on the upper abrasive structure with sufficient force. In this way, once the upper abrasive structure is used or becomes dirty, a user can remove it by exposing a clean abrasive structure underneath. In this way, the scrubbing product is "able to cool".
In one embodiment, for example, the coupling structure may comprise a plurality of stitches such that the abrasive structures are held together by a thread. The thread can be, for example, an elastic yarn made of an elastic material. In a particular embodiment, the stitches are located around the perimeter of the abrasive structures. To facilitate the removal of the upper abrasive structure, each abrasive structure can also be drilled where the stitches are located or elsewhere to allow release when the abrasive structures are pulled.
In an alternative embodiment, the coupling structure may comprise hook and loop couplings located between adjacent layers of the abrasive structures. For example, each abrasive structure may comprise an abrasive layer coupled to a fibrous cellulose fabric. The abrasive layer may include hooks that will engage the cellulose fabric when the abrasive structures are stacked.
In another embodiment, a loop material may be coupled to the cellulose fabric opposite the abrasive layer. In this embodiment, the curl material can also serve as a scrubbing surface if desired.
In yet another alternative embodiment of the present invention, the coupling structure may comprise coupling points attached at points located between the adjacent abrasive structures. The coupling points joined by a point can be constructed of an adhesive. In an alternative embodiment, the coupling points can be made by blowing with fusing the layers of abrasive structures together.
In another embodiment of the present invention, the coupling structure may comprise snaps, closure type coupling means (ZIP-LOC) and the like.
Any of the above coupling structures can be used alone or in combination with other embodiments mentioned above.
The scrubbing product of the present invention can be useful in very different applications. For example, a scouring pad may be useful as a tack cloth, a scouring pad, a sponge, a polishing pad, a sanding pad, or a personal cleansing pad, such as an exfoliation pad. In addition, the scrubbing product may be part of a cleaning tool (such as a mop, etc.) useful for cleaning floors, walls, windows, toilets, and the like.
In certain embodiments, the product of the present invention may include the abrasive layer alone, without any absorbent layer. For example, a meltblown or spunbonded layer alone can be used as a scouring pad, a polishing pad, a sanding pad, or a personal cleansing pad such as an exfoliation pad, for example, with either or without the absorbent layer attached.
Definitions As used herein, the term "coform fabric" means a process in which at least one meltblown matrix head is arranged near a hopper through which other materials are added to the fabric while it is in formation. Such other materials can include pulp, super absorbent particles, natural or synthetic basic fibers, for example. The coform processes are shown in commonly assigned U.S. Patent Nos. 4,100,324 issued to Anderson et al .; 4,818,464 awarded to Lau. The tissues produced by the coform process are generally referred to as coform materials.
As used herein, the term "meltblown fibers" means the fibers or micro-fibers formed by the extrusion of a molten thermoplastic material through a plurality of thin and usually circular capillary matrix vessels with strands or filaments fused to the inside. of gas jets heated at high speed (for example, air) and converging that attenuate the filaments of molten thermoplastic material to reduce its diameter. After this, the meltblown fibers are carried by the high speed gas jet and are deposited on a collecting surface to form a randomly dispersed meltblown fabric. The melt blown fibers can be continuous or discontinuous and are generally tacky when deposited on a collecting surface. In some embodiments, however, low or minimum air flow is used to reduce the attenuation of the fiber and, in some embodiments, to allow neighboring filaments of molten polymer to melt (e.g., to adhere along the the respective sides of the strands), being joined at least in part along the proximal sides of the neighboring strands to form fibers that are elongated fibers of multiple strands (eg, an aggregate fiber formed of two or more polymer strands also defined here).
As used herein, "papermaking fibers" include all known cellulose fibers or fiber blends comprising cellulose fibers. Suitable fibers for making the fabrics of this invention comprise any natural or synthetic cellulose fiber including, but not limited to non-woody fibers, such as cotton, abaca, kenaf, sabai grass, flax, esparto, straw, jute, bagasse, fibers of milkweed fluff, and pineapple fiber; fibers that include soft wood, such as soft wood kraft fibers from the north and south; hardwood fibers, such as eucalyptus, maple, birch, and poplar. Woody fibers can be prepared in the form of high productivity or low productivity and can be pulped from any known method, including kraft, sulfur, high productivity pulping methods and other known pulping methods. Fibers prepared by organogenic pulping methods can also be used. A part of the fibers, such as up to 50% or less by dry weight, or from about 5% to about 30% by dry weight, can be synthetic fibers such as rayon, polyolefin fibers, polyester fibers, fibers sheath and core bicomponents, multi-component binder fibers, and the like. An exemplary polyethylene fiber is Pulpex®, available from Hercules, Inc. (of Wilmington, Delaware). Any known bleaching method can be used. The types of synthetic cellulose fiber include rayon in all its varieties and other fibers derived from viscose or chemically modified cellulose. The chemically treated natural cellulose fibers can be used such as mercerized pulps, cross-linked or chemically-bonded fibers, or sulfonated fibers. For good mechanical properties in the use of papermaking fibers, it may be desirable for the fibers to be relatively undamaged and greatly unrefined or only slightly refined. While recycled fibers can be used, virgin fibers are generally useful for their mechanical properties and lack contaminants. Mercerized fibers, regenerated cellulose fibers, cellulose produced by microbes, rayon, and other cellulose material or cellulose derivatives can be used. Suitable papermaking fibers may also include recycled fibers, virgin fibers, or mixtures thereof. In certain embodiments capable of high volume and good compressive properties, the fibers may have a Canadian Standard Freedom of at least 200, more specifically of at least 300, more specifically still of at least 400, and more specifically of at least 500.
As used herein, the term "high production pulp fibers" are those papermaking fibers produced by pulping processes that provide a production of about 65 percent or more, more specifically about 75 percent or greater , and even more specifically from around 75 to around 95 percent. Production is the resulting quantity of processed fiber expressed as a percentage of the initial mass of wood. Such pulping processes include bleached quimotermomechanical pulp (BCTMP), quimotermomechanical pulp (CTMP), pressure / pressure thermomechanical pulp (PTMP), thermomechanical pulp (TMP), thermomechanical chemical pulp (TMCP), high production sulfide pulps, and high production kraft pulp, all of which leave the resulting fibers with high lignin levels. High production fibers are well known for their stiffness (in both dry and wet states) in relation to typical fibers made chemically pulped. The cell wall of kraft fibers or other fibers of non-high production tend to be more flexible because the lignin, the "mortar", or "glue" on or in part of the cell wall has been greatly removed. Lignin is also not able to swell in water and is hydrophobic, and resists the softening effect of water on the fiber, maintaining the stiffness of the cell wall in high production wet fibers in relation to kraft fibers. Preferred high production pulp fibers can also be characterized as being comprised of comparatively whole, relatively undamaged, high freedom fibers (250 Canadian Standard Freedom (CSF) or higher, more specifically 350 Canadian Standard Freedom (CSF) or higher, and even more specifically from 400 Canadian Standard Freedom (CSF) or higher, such as from about 500 to 750 Canadian Standard Freedom (CSF)), a content of low finesse (less than 25 percent, more specifically less than 20 percent). percent, even more specifically less than 15 percent, and even more specifically less than 10 percent for the Britt jar test). In addition to the common papermaking fibers listed above, high production pulp fibers also include other natural fibers such as milkweed fluff, abaca, jute, cotton, and the like.
As used herein, the term "cellulose" means including any material that has cellulose as a significant constituent, and especially that comprises about 20 percent or more by weight of cellulose or cellulose derivatives, and more specifically of about 50 percent or more by weight of cellulose or cellulose derivatives. Therefore, the term includes cotton, typical wood pulps, non-woody cellulose fibers, cellulose acetate, cellulose triacetate, rayon, viscous fibers, thermomechanical wood pulp, chemical wood pulp, deagglomerated chemical wood pulp, lyocell and other fibers formed from cellulose solutions in NMMO, algondoncillo, or bacterial cellulose, lyocell, and can be viscose, rayon, and the like. The fibers that have not been spun or regenerated from the solution can be used exclusively, if desired, or at least about 80% of the fabric can be free of spun fibers or fibers generated from a cellulose solution. Examples of cellulose fabrics may include known tissue material or fibrous related tissue, such as wet creped tissue, uncropped tissue placed wet, patterned or patterned tissue such as Bounty® paper towels or Charmin® toilet paper made by Procter & Gamble (from Cincinnati, Ohio), facial tissue, toilet paper, dry-laid cellulose fabrics, such as air-laid fabrics comprising binder fibers, coform fabrics comprising at least 20% paper fibers or at least 50% of fibers for making paper, tissue formed by foam, cleaning cloths for home and industrial use, hydroentangled fabrics such as hydroentangled spunbond fabrics with papermaking fibers, exemplified by the fabrics of U.S. Patent No. 5,284,703, issued February 8, 1994 to Everhart et al., and the United States patent. United States of America number 4,808,467, granted on February 28, 1989 to Suskind and others, and the like. In one embodiment, the cellulose fabric can be a reinforced cellulose fabric comprising a synthetic polymer network such as a spunbonded fabric to which the papermaking fibers are added by lamination, adhesive bonding, or hydroentanglement, or which an adhesive such as latex has been impregnated into the fabric (eg, by engraved printing or other known means, exemplified by the VIVA® paper towel from Kimberly-Clark Corp. of Dallas, Texas) to provide tensile strength of high humidity or dry to the tissue. The reinforced polymer (including the adhesive) may comprise about 1% or more of the cellulose tissue mass, or any of the following: about 5% or greater, about 10% or greater, about 20% or greater, about 30% or greater, or about 40% or greater, of the cellulose tissue mass, such as from about 1% to about 50% or from about 3% to about 35% of the cellulose tissue mass.
As used herein, "vacuum volume" refers to the volume of space occupied by a sample that does not comprise solid matter. When expressed as a percentage, it refers to the percentage of the total volume occupied by the sample that does not comprise solid matter.
The "Total Surface Depth" is a measure of the topography of a surface, indicative of a different characteristic height between elevated and depressed parts of the surface. The optical technique used to measure the Total Surface Depth is described here after.
Brief Description of the Figures A complete and authoritative description of the present invention, including the best mode thereof for one of ordinary skill in the art, is pointed out more particularly in the remainder of the specification, including references to the accompanying figures in which: Figure 1 is a schematic diagram of an embodiment of a process line for making the abrasive layer of the present invention.
Figure 2 is a diagram of an embodiment of a process for forming non-creped continuous dried paper fabrics as may be used in the present invention.
Figure 3 is a schematic diagram of an incorporation of a process line to make the construction of the compound of the present invention.
Figure 4 is an embodiment of a process for combining the layers of the construction of the compound of the present invention.
Figure 5 is another embodiment of a process for combining the layers of the construction of the compound of the present invention.
Figure 6 is a perspective view of an embodiment of a scouring pad of the present invention.
Figure 7 is a cross-sectional view of an embodiment of the scouring pad of the present invention.
Figure 8 is a cross-sectional view of another embodiment of the scouring pad of the present invention.
Figure 9 is a cross-sectional view of another embodiment of the scouring pad of the present invention.
Figure 10 is a perspective view of an embodiment of a cleaning pad of the present invention wherein the scrubbing pad is held on a rigid gripper.
Figure 11 depicts cross sections of a fiber formed from a single polymer strand and a multi-strand aggregate formed of six melted strands.
Figure 12 depicts a cut portion of a meltblown matrix.
Figure 13 is a perspective view of an embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 14 is another perspective view of a scrubbing product illustrated in Figure 13.
Figure 15 is a perspective view of another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 16 is a perspective view of yet another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 17 is another embodiment of a scouring product made in accordance with the present invention that includes a plurality of abrasive structures.
Figure 18 is a perspective view of another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 19 is a cross-sectional view of another embodiment of a scrubbing product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 20 is a perspective view of yet another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 21 is a perspective view of yet another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 22 is a perspective view with cut-away portions of another embodiment of a scouring product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 23 is a perspective view of another embodiment of a scrubbing product made in accordance with the present invention containing a plurality of abrasive structures.
Figure 24 describes a starting point for the Abrasion Index Test; Y Figure 25 describes a representative topographic profile as an illustration of the concepts of the material line.
The repeated use of reference characters in the present specification and drawings is intended to represent the same or analogous features or elements of the present invention.
Detailed Description of Preferred Additions Reference will now be made in detail to the embodiments of the invention, one or more examples of which are indicated below. Each example is provided by way of explanation of the invention, is not limitation of the invention. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the scope or spirit of the invention. For example, the features illustrated or described as part of an embodiment may be used in another embodiment to produce still further incorporation. Therefore, it is intended that the present invention cover such modifications and variations as come within the scope of the appended claims and their equivalents.
In general, the present invention is directed to disposable scouring pads that are suitable for use in a wide variety of applications, including home cleaning and personal care applications. For example, the scouring products of the present invention may be suitable for use as a kitchen cloth, an all-purpose cleaning cloth, a scouring pad or a polishing pad, or a personal care product, such as a pad of exfoliate, for example. Scrubbing products can also be used in a mop, such as a mop head capable of being replenished. The mop can be used in dry or wet applications. In certain embodiments, the scouring products of the present invention can be used to remove layers from a surface, for example in a sanding or polishing application.
The scouring pads of the present invention are generally of a multilayer construction and include a non-woven abrasive layer secured to an absorbent layer that includes one or more layers of a non-woven fabric. For example, the abrasive layer may be a porous, flexible, meltblown fabric and may be thermally bonded to one or more layers of a high volume absorbent paper fabric, such as a continuously dried, non-creped paper fabric. (UCTAD).
The two different layers of scouring pad compound can offer cleaning advantages beyond those known in other scouring compounds, and can do so at much lower cost. Other advantages are also obtained by the disposable scrubbing pads. For example, the soft paper fabric and pad flexibility can make the article much more comfortable to hold during cleaning than previously known scouring compound articles. Additionally, the pads can be formed to be dockable for either heavy or light scrubbing, as desired by the user. For example, a cleaning tool capable of holding the scrubbing product of the present invention can be used to clean floors, walls, windows, lavatories, ceiling fans, and the like as well as to clean surfaces by polishing or sanding a surface.
If desired, scouring pads may optionally include various additives, such as cleaning or medication agents, which can improve the performance of the pads. Of particular advantage, it has been discovered that a synergy may occur between the component layers of the structure of the compound of the present invention, and the scrub pads may exhibit mechanical properties greater than the sum of the mechanical properties of the individual layers. For example, tensile strength and durability, among other mechanical properties, may be greater in the structure of the composite than the sum of the same properties in the individual layers. Similarly, abrasion of the pad on the abrasive surface can be improved due to the texture of the coupled absorbent layer.
In general, the abrasive layer of the scouring pads of the present invention may include a material that is formed in an open, porous structure and has sufficient strength and hardness to form a rough, scraping surface on the pad. Suitable materials are plentiful and can be either natural or synthetic materials. Possible exemplary materials can include any known abrasive material formed in the desired open structure. Possible synthetic materials can be polymeric materials, such as, for example, nonwoven melt blown fabrics formed of molten or uncured polymer which can be cured to form the desired abrasive layer.
Other materials can optionally be used as the abrasive layer of the present invention. For example, other materials used as abrasives in known commercial scrubbing products may be used, such as perforated nylon covers, nylon nets, and materials similar to those found in other abrasive products such as, for example, the SCOTCHBRITE pads of the 3M Corporation (Minneapolis, Minnesota).
The materials and processes used to form the abrasive layer of the scouring pad can be chosen and designed having in mind the desired purpose of use of the product. For example, a scouring pad designed as a personal care product, such as a face wash pad, may include an abrasive layer that is softer and less abrasive than a scouring pad for use in home cleaning applications. . Therefore, the raw materials, additives, diameter of the fiber, density and stiffness of the layer, etc., can all vary depending on the desired characteristics of the final product.
In one embodiment, the abrasive layer of the scouring pad may include a spunbond fabric, such as may be formed using a thermoplastic polymer material. Generally, any suitable thermoplastic polymer that can be used to form the nonwoven melt blown fabrics can be used for the abrasive layer of the scrub pads. A non-exhaustive list of possible thermoplastic polymers suitable for use includes polymers or copolymers of polyolefins, polyester, polypropylene, high density polypropylene, polyvinyl chloride, vinylidene chloride, nylon, polytetrafluoroethylene, polycarbonate, poly) methyl) acrylates, polyoxymethylene , polyesters, ABS, polyether ester, or polyamides, polycaprolactane, thermoplastic starch, polyvinyl alcohol, polylactic acid, such as, for example, polyester ida (optionally with glycerin as a plasticizer), polyphenylsulfide (PPS), polyether ketone (PEEK), polyvinylidenes , polyurethane, and polyurea. For example, in one embodiment, the abrasive layer may include nonwoven meltblown fabrics formed with a polyethylene or a polypropylene thermoplastic polymer. The polymer alloys can also be used in the abrasive layer, such as polypropylene alloy fibers and other polymers such as polyethylene terephthalate (PET). The compatibilizers may be needed for some polymer combinations to provide an effective blend. In an incorporation, the abrasive polymer is substantially free of halogenated compound. In another embodiment, the abrasive polymer is not a polyolefin, but comprises a material that is more abrasive than say, polypropylene or polyethylene (for example, having flexible modules of about 1200 megapascal (MPa) and larger, or a hardness Shore D of 85 or greater).
Thermoset polymers can also be used, as well as photo curable polymers and other curable polymers.
In addition to being harsh, the fibers of the abrasive layer may have a high elastic modulus, such as an elastic modulus scarcely equal to or greater than that of the polypropylene, such as about 1,000 megapascal (MPa) or greater, specifically about 2,000. megapascals (MPa) or greater, more specifically around 3,000 megapascals (MPa) or greater, and more specifically about 5,000 megapascals (MPa) or greater. As an example, phenol plastics can have elastic moduli of around 8,000 megapascals (MPa), and a reinforced polyamide (nylon 6, 6) with 15% fiberglass has a reported elastic modulus of around 4,400 megapascals ( MPa) (while the elastic modulus is around 1,800 megapascals (MPa) without the glass reinforcement).
The fibers of the abrasive layers may be elastomeric or non-elastomeric, as desired (eg, crystalline or semi-crystalline). In addition, the abrasive layer may comprise a mixture of elastomeric fibers and non-elastomeric fibers.
For some polymer groups, an increased melting point can be correlated with improved abrasive characteristics. Thus, in one embodiment, the abrasive layers may have a melting point greater than 120 degrees centigrade, such as about 140 degrees centigrade or greater, of about 160 degrees centigrade or greater, of about 170 degrees centigrade or greater , about 180 degrees centigrade or greater, or about 200 degrees centigrade or greater, exemplified by the following ranges: from around 120 degrees centigrade to around 350 degrees centigrade, from around 150 degrees centigrade to around 250 degrees centigrade, or from around 160 degrees Celsius to around 210 degrees Celsius.
In some embodiments, polymers with relatively high viscosity or low melt flow rates may be useful in producing rough fabrics for effective cleaning. The melt flow rate of the polymer is measured in accordance with the test of the American Society for Testing and Materials (ASTM) D-1238. While polymers typically used in meltblowing operations may have melt flow rates of about 1000 grams per 10 minutes or greater and may also be considered in some embodiments of the present invention, in some embodiments the polymers used to produce the layer abrasive may have a melt flow rate in accordance with the American Society for Testing and Materials (ASTM) D-1238 test, of less than about 3000 grams per 10 minutes or 2000 grams per 10 minutes, such as less about 1000 grams per 10 minutes or less than about 500 grams per 10 minutes, specifically less than 200 grams per 10 minutes, more specifically less than about 100 grams per 10 minutes, and more specifically less than about 80 grams per 10 minutes, such as from about 15 grams per 10 minutes to about 250 grams per 10 minutes, or from about 20 grams for 10 minutes at around 400 grams per 10 minutes.
Another measure that can be indicative of good abrasive properties is the Shore D Hardness, as measured by the standard test method of the American Society for Testing and Materials (ASTM) D 1706. In general, a suitable polymeric material of the layer abrasive may have a Shore D Hardness of about 50 or greater, such as about 65 or greater, or more specifically, about 70 or greater, or more specifically about 80 or greater. Polypropylene, for example, typically has Shore D hardness values from about 70 to about 80.
In one embodiment, the polymeric material in the abrasive layer may have a flexural modulus of about 500 megapascals (MPa) or greater and a Shore D hardness of about 50 or greater. In an alternative embodiment, the polymeric material may have a flexural modulus of about 800 megapascals (MPa) or greater and a Shore D hardness of about 50 or greater.
In one embodiment, the polymer fibers of the abrasive layer are substantially free of plasticizers, or may have 33 percent by weight of plasticizer or less, more specifically about 20 percent by weight of plasticizer or less, more specifically about 3 percent by weight or less. The dominant polymer in the polymer fibers may have a molecular weight of any of the following: about 100,000 or greater, about 500,000 or greater, about 1,000,000 or greater, about 3,000,000 or greater, and about 5,000,000 or greater.
The abrasive layer may comprise fibers of any suitable cross section. For example, the fibers of the abrasive layer may include rough fibers with circular or non-circular cross sections. In addition, the fibers of the non-circular cross section may include fibers with slots or multi-lobed fibers, such as for example, "4DG" fibers (especially, deep-groove fibers of polyethylene terephthalate (PET), with a shape of cross section of eight legs). Additionally, the fibers can be single-component fibers, formed from a single polymer or copolymer, or can be multi-component fibers.
In an effort to produce an abrasive layer having desirable combinations of physical properties, in an embodiment, non-woven polymer fabrics made of filaments and multicomponent or bicomponent fibers can be used. The bicomponent or multi-component polymer fibers or filaments include two or more polymeric components that remain distinct. The various components of the multi-component filaments are arranged in substantially different areas across the cross section of the filaments and extend continuously along the length of the filaments. For example, bicomponent filaments may have a side-by-side or sheath and core arrangement. Typically, one component exhibits different properties than another in such a way that the filaments exhibit properties of two components. For example, one component may be polypropylene which is relatively strong and the other component may be polyethylene which is relatively soft. The final result is a strong yet non-woven fabric.
In one embodiment, the abrasive layer comprises metallocene polypropylene or "single-site" polyolefins for improved strength and abrasion. Single-site material copies are available from H.B. Fuller Company, from Vadnais Heights, Minnesota.
In another embodiment, the abrasive layer includes a precursor fabric comprising a planar non-woven substrate having a distribution of attenuated thermoplastic fibers capable of melting such as the polypropylene fibers therein. The precursor fabric may be heated to cause the thermoplastic fibers to shrink and form remnants of nodulated fiber imparting an abrasive character to the resulting fabric material. The remains of the nodulated fiber may comprise between about 10% and about 50% by weight of the total fiber content of the fabric and may have an average particle size of about 100 micro meters or greater. In addition to the fibers that are used to form nodular moieties, the precursor fabric may contain cellulose fibers and synthetic fibers having at least one component with a higher melting point than polypropylene to provide strength. The precursor tissue can be placed wet, placed by air, or made by other methods. In one embodiment, the precursor fabric is substantially free of papermaking fibers. For example, the precursor fabric may be a fibrous nylon fabric containing polypropylene fibers (for example, a bonded and carded fabric comprising both nylon fibers and polypropylene fibers).
The material used to form the abrasive layer may also contain various additives as desired. For example, various stabilizers may be added to a polymer, such as light stabilizers, heat stabilizers, processing aids, and additives that increase the thermal stability of polymer aging. In addition, auxiliary wetting agents, such as hexanol, antistatic agents such as potassium alkyl phosphate, and alcohol repellents such as various fluoro polymers (eg, the DuPont 9356H repellent) may also be present. Desirable additives may be included in the abrasive layer either through the inclusion of the additive to a polymer in the matrix or alternatively through the addition to the abrasive layer after its formation, such as through a spraying process.
For example purposes, an embodiment of a system for forming a nonwoven meltblown fabric as may be used in the abrasive layer of the scrub pad is illustrated in Figure 1. As shown, the system includes a forming machine generally 110 that can be used to produce a meltblown fabric 32 in accordance with the present invention. Particularly, the forming machine 110 includes an endless band of foraminous formation 114 wrapped around the rollers 116 and 118 such that the web 114 is driven in the direction shown by the arrows.
The forming web 114 may be any suitable forming web and, if desired, may provide additional three dimensional texture to the meltblown layer. Added texture can affect the abrasion of the layer. For example, a high degree of surface texture in the melt blown layer can be achieved by the formation of a meltblown layer on a high dimension forming fabric, such as those available from Lindsay Wire Company.
If the melt blown fibers are melted or partially melted when they strike the wire, the texture of the wire can be imparted to the fabric, particularly with the assistance of hydraulic pressure through the wire for further pressure of the blown fibers with melting against the wire before they completely solidify. Improved molding of the blown fibers with melting against the wire can be achieved by using a suitable high polymer temperature or air jet temperature, and / or by adjusting the distance between the meltblown matrix and the conveyor wire. The conveyor wire can have a repeated series of depressions which can correspond to high regions on the meltblown fabric useful for cleaning. A three-dimensional conveyor wire can impart high meltblown structures that raise about 0.2 millimeters or greater of the blown fabric with surrounding melt, more specifically about 0.4 millimeters or greater, depending on the desired level of abrasion. A spectrum of pads can be produced for scrubbing from medium abrasion to aggressive abrasion.
The repeated structures can be represented as the minimum characteristic of the unit cell of the conveyor wire, and the unit cell can have a minimum length scale in plane (for example, for the unit cell which is a parallelogram, the length of the side shorter, or for more complex shapes such as a hexagon, smaller than the width in the machine direction and width in the transverse direction) of about 1 millimeter or greater, such as about 2 millimeters or greater, or it may have an area of about 5 square millimeters or greater (for example, a unit cell of dimensions of 1 millimeter by 5 millimeters) or of about 20 millimeters square or larger. A carrier wire can be treated with a release agent such as a silicon liquid or coated with Teflon® or other release agents to improve the removal of the blown tissue with texturized melting of the transport wire.
Figure 8 is a cross section of an embodiment of the present invention illustrating a highly textured meltblown layer 32 as it can be formed on a highly textured fabric. The blown layer with highly textured fusion can then be coupled to an absorbent layer 34 in the formation of the scrub pad of the present invention.
The forming machine system of Figure 1 may also include a matrix 120 which is used to form fibers 126. The flow rate of the matrix 120 is specified in pounds of polymer melt per inch of the width of the matrix per hour (PIH) . As the thermoplastic polymer leaves the matrix 120, high pressure fluid, usually air, attenuates and distributes the polymer jet to form the fibers 126. The fibers 126 can be randomly deposited on the forming web 114 and form the layer blown with fusion 32.
In the manufacture of conventional meltblown materials, high velocity air is usually used to attenuate the polymeric strands to create thin, fine fibers. In the present invention, by adjusting the air flow system, such as increasing the air flow area or otherwise decreasing the velocity of the air jet immediately adjacent to the molten polymer strands as they emerge from the head of the melt blown, possible to prevent substantial attenuation of fiber diameter (or reduce the degree of fiber attenuation). Limiting the attenuation of the diameter of the fiber can increase the roughness of the fiber, which can increase the abrasion of the layer formed by the fibers.
Additionally, the air flow near the outlet of the matrix can be used to agitate and distribute the polymer fibers in a manner that can be highly non-uniform in the forming web. The high degree of non-uniformity of the placement of blown fibers with rough fusing on the web may manifest itself in a fabric that may exhibit variations in thickness and variations in the basis weight across the surface of the fabric, for example, an uneven surface It can be created in the fabric, which can increase the abrasion capacity of the layer formed by the fibers.
In addition, the non-uniform distribution of the fibers during tissue formation can create a tissue that increases the vacuum space within the tissue. For example, an open network of fibers can be formed that can have voids that occupy a substantial part of the layer. For example, the vacuum volume of the abrasive layer may be greater than about 10%, particularly greater than about 50%, and more particularly greater than about 60% of the volume of the material. These open vacuum materials can inherently have good scrubbing properties.
The abrasive layer may also have a relatively open structure that provides high permeability, allowing the gas or liquid to readily pass through the abrasive layer. The permeability can be expressed in terms of Air Permeability measured with the FX 3300 Air Permeability device manufactured by Textest AG (from Zurich, Switzerland), set at a pressure of 125 Pascals (Pa) (0.5 inches of water) with the opening normal of 7 centimeters in diameter (38 square centimeters), operating under environmental conditions of the Technical Association of the Pulp and Paper Industry (TAPPI) (73 degrees Fahrenheit, 505 relative humidity). The abrasive layer may have an Air Permeability of any of the following: about 100 cubic feet per minute (CFM) or greater, of about 200 cubic feet per minute (CFM) or greater, of about 300 cubic feet per minute (CFM) or greater, of around 500 cubic feet per minute (CFM) or greater, of around 700 cubic feet per minute (CFM) or greater, such as from about 250 cubic feet per minute (CFM) at around 1,500 cubic feet per minute (CFM) or greater, or from around 150 cubic feet per minute (CFM) to around 1000 cubic feet per minute (CFM) or from around 100 cubic feet per minute ( CFM) at around 1000 cubic feet per minute (CFM), or from around 100 cubic feet per minute (CFM) to around 800 cubic feet per minute (CFM), or from around 100 cubic feet per minute (CFM) to around 500 cubic feet per minute (CFM).
Alternatively, the Air Permeability of the abrasive layer can be less than about 400 cubic feet per minute (CFM). In cases where the abrasive layer has a basis weight of less than 150 grams per square meter (gsm), multiple layers of the abrasive layer having a combined basis weight of at least 150 may exhibit an Air Permeability of about 70 cubic feet. per minute (CFM) or greater, or any of the aforementioned values or ranges given for a single abrasive layer.
The void space or pores created in the fabric can also produce variations in the opacity through the fabric in such a way that the abrasive layer formed by the fabric can be somehow translucent. Due to the random placement of the fibers and the resulting open structure of the abrasive layer, many of the pores formed in the fabric can extend through the entire depth of the layer, allowing light to pass through the layer without obstacle and providing a degree of translucence of the abrasive layer. In certain embodiments, more than about 30% of the surface area of the abrasive layer may include open void space that extends through the axial depth of the layer. More specifically, more than about 50% of the surface area of the abrasive layer can include open void space that extends through the axial depth of the layer, providing a high degree of translucence to the abrasive layer. As such, a significant percentage of the surface area of the abrasive layer can be occupied by openings or pores through which the underlying absorbent layer can be seen. For example, about 10% or greater, specifically about 20% or greater, more specifically about 40% or greater, and more specifically about 55% or greater of the surface area of the abrasive layer (the surface area seen in plan view from above) can be occupied by openings through which the underlying absorbent layer can be seen. Additionally, the abrasive layer can be formed of a translucent polymer that can increase the translucency of the layer.
Expressed on a percentage basis, the standard deviation of opacity for data points averaging about 5 millimeters of square sections can be about 5% or more, more specifically about 10% or more, more specifically about 20%. % or greater, and more specifically about 30% or greater, such as from about 8% to about 60%, or from 12% to about 50%.
Other additives, fillers, and pigments known in the art may also be combined with the polymers in the abrasive layers of the present invention. Polymeric fibers reinforced with glass or other minerals, in any of the five or in the form of a particle, are within the scope of the present invention. For example, fibers containing mineral or glass or other forms of fiber components may comprise about 50 weight percent or more of synthetic polymer, more specifically about 60 weight percent or more of synthetic polymer, more specifically about 80 percent by weight or more of synthetic polymer, and more specifically from about 90 percent by weight to add 99 percent by weight of synthetic polymer.
In general, the thermoplastic polymer fibers in the abrasive layer can be larger than about 30 microns in average diameter. More specifically, the thermoplastic fibers may be between about 40 microns and about 800 microns in average diameter, such as from about 50 microns to about 400 microns, more specifically from about 60 microns to about 300 microns, and more specifically from about 70 micras to about 250 micras. Such fibers are substantially rougher than the fibers of conventional melt blown fabrics, and the added roughness is generally useful in increasing the abrasive characteristics of the fabric.
The fibers that form the meltblown fabric may be long enough to support the open network of the layer. For example, the fibers can have a fiber length of at least about one centimeter. More specifically, the fibers may have a characteristic fiber length of greater than about 2 centimeters.
If desired, the fibers may optionally be formed to include improved abrasion characteristics, such as the inclusion of filler particles, e.g., microspheres, pumice or metal granules, meltblown "injection" treatment, and the like. .
The microspheres can be from about 10 microns to about 1 millimeter in diameter and typically have a carapace thickness from about 1 to about 5 microns, while the macro-spheres (which can also be used in some embodiments) They can have diameters greater than about 1 millimeter. Such materials may include micro-drops of metal, glass, carbon, mica, quartz, or other minerals, plastic such as acrylic or phenolic, including acrylic microspheres known as PM 6545 available from PQ Corporation, of Pennsylvania, and micro- hollow spheres such as the cross-linked acrylate SunSpheres ™ from ISP Corporation (of Wayne, New Jersey) and similar hollow spheres as well as expansive spheres such as Expance® microspheres (from Expancel, Stockviksverken, Sweden, a division of Akzo Nobel , of the Netherlands), and the like.
In an embodiment of the present invention, the abrasive layer can be made of a non-woven fused spun fabric, such as a meltblown fabric treated with a "injection" blown with fusion. The meltblown injection is a rough non-uniform layer applied in a melt blown process deliberately operated to generate random beads of the polymer (typically polypropylene or other thermoplastic) interconnected with yarns. If desired, the injection can be distinctively colored to make the abrasive element readily visible.
Optionally, the abrasive layer of the present invention can be formed of two or more different types of fiber. For example, the abrasive layer can be formed of different fiber types formed from different polymers or from different polymer combinations. Additionally, the abrasive layer may be formed of fibers of different types including fibers of different orientations, for example, crimped or straight fibers, or fibers having different lengths or diameters of the cross section of each. For example, the matrix 120 can be a multi-section matrix and includes different polymer material in different sections that can be delivered through the matrix 120 and from distinctly different fibers that can then be mixed and heterogeneously distributed over the forming web 114. Alternatively, two or more different meltblown sublayers can be formed and joined together to form an abrasive layer with a homogeneous, fairly uniform distribution or different types of fiber.
In one embodiment, the abrasive layer of the present invention may include multi-filament aggregates of individual polymeric yarns.
As used herein, the term "multi-strand aggregate" refers to a meltblown fiber that is currently an aggregate of two or more polymer strands formed by at least the partial melting (adhesion) of adjacent extruded molten polymer strands. of adjacent holes on a meltblown matrix, which can be achieved, for example, under circumstances in which turbulence created by air jets is substantially lower than normal meltblowing operation, thus allowing two or more yarns adjacent ones come into contact and join together along at least a part of the length of the threads. For example, individual strands that form the aggregate fiber of multiple strands, can be joined side by side by a distance greater than about 5 millimeters, along the length of the fiber. As such, bicomponent fibers, multi-lobed fibers, and the like, which are extruded as a single fiber with multiple polymers or complex shapes should not be confused with the fibers of the multi-filament aggregate of the present invention, which includes polymer yarns. adjacent extruded or expelled from adjacent holes in the meltblown matrix and only adhered together after leaving the matrix.
The holes of the meltblown matrix can be in one or more rows. When more than one row of holes are present in the matrix, the holes can be alternated or aligned, or distributed in other ways known in the art. The holes of the matrix can be of any desired shape so as to form individual threads of a desired shape of the cross section. Even after bonding together, the individual substantially circular polymer strands may retain elements of their individual circular cross sections.
The multi-filament aggregates may be substantially of the ribbon-in-character type, particularly when three or more threads of adjacent meltblown holes aligned in one line adhere to each other in a substantially parallel array (eg, parallel to each other with the line formed by the connection of the center points of the consecutive threads being in an approximately straight line). For example, Figure 11 illustrates an aggregate of multiple filaments formed of six individual polymer strands adhered in a substantially parallel array. The width of the aggregate of multiple filaments can be about as large as the number of yarns in the aggregates of multiple filaments multiplied by the diameter of a single yarn, even though due to the fusion of the parts of the joined yarns and due to the alternation of the threads in some cases, the width is usually a fraction of the product of the number of threads and only the diameter of the thread (or average diameter of a single thread). This fraction can be formed from about 0.2 to about 0.99, specifically from about 0.4 to about 0.97, more specifically from about 0.6 to about 0.95, and more specifically from about 0.7 to about 0.95. In one embodiment, the main axis of the non-circular multi-strand aggregate fiber of the cross-section may be greater than about 30 microns.
The number of threads in the aggregate of multiple filaments can be in the range from 2 to around 50, specifically from 2 to around 30, more specifically from 2 to around 20, and more specifically from about 3 to about 12 The multi-filament aggregates can have a count of average weight threads numbered 3 or more, 4 or more, 5 or more, or 6 or more. A meltblown fabric comprising multi-filament aggregates can have multi-filament aggregates comprising 5% or greater of the mass of the fabric (such as multi-filament aggregates with three or more yarns comprising 5% or greater of the mass of the tissue). For example, the mass fraction of the fabric consisting of multi-filament aggregates can be about 10% or more, about 20% or more, about 30% or more, about 40% or more, about 50% or greater, about 60% or greater, about 70% or greater, about 80% or greater, about 90% or greater, or substantially 100%. These ranges can apply to aggregates of multiple filaments in general, or to aggregates of multiple filaments that have at least 3 strands, 4 strands, 5 strands, or 6 strands.
Figure 11 depicts cross sections of a polymer fiber 126 formed from a single polymeric yarn 238 in an operation such as meltblowing, and by comparison discloses a cross section of a multi-filament aggregate 240 formed by the partial melt of six yarns 238 to produce a structure of the tape type. The region where two wires 238 are joined together may comprise a cusp 243.
The smallest rectangle 241 that can completely enclose the cross section of the multi-filament aggregate 240 has a width W and a height H. The width W is the width of the aggregate of multiple filaments and the height H is the height of the aggregate of multiple filaments. For many applications, the width can be from around 50 microns to around 800 microns. In other embodiments, however, other widths may be achieved such as widths of about 100 microns or greater, of about 200 microns or greater, of about 400 microns or greater, of about 600 microns or greater, and around 800 micras or more.
The aspect ratio of the multi-filament aggregate is the W / H ratio. The aspect ratio of multi-filament aggregates in the present invention may be about 2 or greater, about 3 or greater, about 4 or greater, about 5 or greater, or about 6 or more. greater, such as from about 3 to about 12.
The strands 238 of the multi-filament aggregate 240 may remain substantially parallel along the entire length of the fiber (a multi-strand aggregate 240), or they may persist for a distance and then be divided into two or more groups of smaller aggregates of multiple strands. or individual threads 238. The threads 238 of the multi-filament aggregate 240 can remain attached to one another along their sides by a distance of about 1 millimeter or greater, 5 millimeters or greater, 10 millimeters or greater, 20 millimeters or greater, or 50 millimeters or greater.
Referring again to Figure 1, the forming web 114 may be any suitable forming web and, if desired, may provide texture to the meltblown layer, which may affect the abrasion of the layer.
For example, a high degree of surface texture in the meltblown layer can be achieved by the formation of the meltblown layer on a high dimension fabric, such as that available from Lindsay Wire Company. In another embodiment, the abrasive layer can be formed directly on the fibrous absorbent fabric (not shown), such as a textured tissue or other cellulose fabric, which can be carried on a fabric. Figure 8 is a cross-section of an embodiment of the present invention with a highly textured melt-blown layer 32 coupled to a relatively flat absorbent layer 3. Alternatively, the forming band 114 may be relatively flat and produces a flat melt blown layer 32, as illustrated in Figure 7.
The abrasive layer may have a suitable fiber basis weight and the formation as to provide good scrubbing characteristics to the structure of the composite pad while remaining flexible. For example, a meltblown fabric that forms the abrasive layer may have a basis weight greater than about 10 grams per square meter. More specifically, the melt blown fabric can have a basis weight of between about 25 grams per square meter (gsm) and about 400 grams per square meter (gsm), more specifically between about 30 grams per square meter (gsm) and about 200 grams per square meter (gsm), and more specifically between about 40 grams per square meter (gsm) and 160 grams per square meter (gsm). The meltblown fabric can have a density in the range from either about 0.02 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.06 grams per cubic centimeter, 0.1 grams per cubic centimeter, 0.2 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter, 0.4 grams per cubic centimeter cubic centimeter, 0.6 grams per cubic centimeter, and 0.8 grams per cubic centimeter to any of about 0.1 grams per cubic centimeter, 0.3 grams per cubic centimeter, 0.5 grams per cubic centimeter, and 1 gram per cubic centimeter (other values and known ranges in the art they may also be within the scope of the present invention). In one embodiment, the abrasive layer can be formed in such a way that when the pad is put under pressure, as when a surface is being scrubbed by contact with the abrasive layer, the surface can be substantially in contact with only the melt blown layer. of the pad.
As previously described, the fabric can be formed with variations in thickness and basis weight through the fabric such as to produce a fabric with a more abrasive, uneven surface. Variations in thickness across the surface of the fabric can be measured with a 0.6-inch-diameter plate that is pressed against the sample with a load of 7.3 pounds per square inch (applied pressure of 50 kPa), as it resides in a solid surface, where the displacement of the stage relative to the solid surface indicates the local thickness of the sample. Repeated measurements at different locations in the sample can be used to obtain a distribution of local thickness measurements from which a standard deviation can be calculated. The abrasive layers of the present invention may have a standard deviation in this thickness measurement of at least about 0.2 millimeters, specifically of at least about 0.6 millimeters, more specifically of at least about 0.8 millimeters, and more specifically of at least 1.0 millimeters. Expressed on a percentage basis, the standard deviation of the basis weight for data points averaged over 5-millimeter square sections, may be around 5% or more, more specifically about 10% or more, more specifically around 20% or greater, and more specifically about 30% or greater, such as from about 8% to about 60%, or from about 12% to about 50%.
The abrasion capacity of the abrasive layer can also be improved by the topography of the abrasive layer. For example, the abrasive layer may have a plurality of raised and depressed regions due to uneven base weight, non-uniform thickness, or due to the three-dimensional topography of an underlying fibrous tissue such as a tissue of textured wet laid tissue. The raised and depressed regions may be spaced apart substantially periodically in at least one direction such as machine direction or transverse direction with a characteristic wavelength of about 2 millimeters or greater, more specifically about 4 millimeters or greater, and having a characteristic height difference between the high and low regions of at least 0.3 millimeters or greater, more specifically of about 0.6 millimeters or greater, more specifically of about 1 millimeter or greater, and more specifically of about 1.2 millimeters or older.
In another embodiment, the abrasive layer may include a precursor fabric comprising a planar nonwoven substrate, having a distribution of melt-capable attenuated thermoplastic fibers, such as polypropylene fibers therein. The precursor fabric can be heated to cause the thermoplastic fibers to shrink and form remnants of fiber in nodules to impart an abrasive character to the resulting fabric material. The fiber remnants in the nodule may comprise between about 10% and about 50% by weight of the total fiber content of the fabric and may have an average particle size of about 100 microns or greater. In addition to the fibers that are used to form remnants in nodules, the precursor fabric may contain cellulose fibers and synthetic fibers having at least one component with a higher melting point than polypropylene to provide strength. The precursor tissue can be placed wet, placed by air, or made by other methods. In one embodiment, the precursor fabric is substantially free of papermaking fibers. For example, the precursor may be a fibrous nylon fabric containing polypropylene fibers (for example, a bonded and carded fabric comprising both nylon fibers and polypropylene fibers).
The abrasive layer can also be perforated to improve fluid access to the absorbent layer of the article.
Perforated melt-blown fabrics, for example, may have increased abrasion capacity due to the presence of openings.
Other materials may optionally be used as the abrasive layer of the present invention. For example, other materials used as abrasives in known commercial scrubbing products may be used, such as perforated nylon covers, nylon nets, and materials similar to those found in other abrasive products such as, for example, SCOTCHBRITE pads from 3M Corp. (from Minneapolis, Minnesota).
In accordance with the present invention, an abrasive layer can be secured to one or more absorbent layers, such as those formed by a nonwoven paper fabric, to form a disposable scouring pad. When the laminates according to the present invention are used for scrubbing or other demanding tasks, the durability of the product can be surprisingly high. At least part of the excellent performance can be due to a synergy in the properties of the laminate material, which may be higher than what one can expect based on the material properties of the individual components. For example, the tensile strength and drawing properties of an abrasive laminate comprise a meltblown layer bonded to a tissue of tissue that may have a substantially higher tensile strength than a non-bonded combination of the same meltblown layer and the tissue tissue together.
For some additions, the Resistance Synergy was around 1.05 or greater, more specifically around 1.1 or greater, more specifically around 1.2 or greater, and more specifically around 1.5 or greater, with exemplary ranges of around 1.05 to about 3, from about 1.1 to about 2.5, and from about 1.5 to about 4. For some additions, the Resistance Synergy can be around 1.1 or greater, more specifically around 1.3 or greater , more specifically about 1.5 or greater, and more specifically about 1.8 or greater, with exemplary ranges from about 1.3 to about 3, from about 1.5 to about 2.5, and from about 1.5 to about 2 A laminate with a Resistance Synergy substantially greater than 1 may have but not need to have a Strength Synergy substantially greater than 1. Similarly, a laminate with a Synergy of Re Substantially greater than 1 may have but not need to have a Resistance Synergy substantially greater than 1.
The paper fabric of the absorbent layer is generally a fabric that contains high volume levels. In addition, the fabric can have a substantial amount of wet strength and wet flexibility for use in wet environments. The tissue paper, if desired, can also be highly textured and have a three dimensional structure, similar to the abrasive layer, as previously described. For example, the paper web can have a Total Surface Depth greater than about 0.2 millimeters, and particularly greater than about 0.4 millimeters. In one embodiment, the paper web may be a commercial paper towel, such as SCOTT® Towel or a VIVA® towel, for example. The SCOTT® Towel, for example, has a wet ratio: tensile strength (ratio of wet tensile strength to dry tensile strength, taken in the cross direction) typically greater than 30% (eg, a set of measurements give a value of 38%), and a VIVA® towel has a wet ratio: dry tensile strength typically greater than 60% (eg, a set of measurements gives a value of 71%) . The wet proportions: dry tensile strength can also be greater than 10%, 20%, 40%, or 50%.
In one embodiment, the paper fabric can be a textured fabric that has been dried in a three dimensional state such that the hydrogen bonding fibers were substantially formed while the fabric is not in a planar, flat state . For example, the fabric can be formed while the fabric is on a highly textured continuous drying fabric or other three dimensional substrate.
In general, the non-creped continuous dried paper web may have a basis weight greater than about 25 grams per square meter. Specifically, the paper web can have a basis weight greater than 40 grams per square meter, more specifically greater than about 50 grams per square meter. If desired, the fabric may include a wet strength agent and / or at least about five percent by weight of high production pulp fibers, such as thermomechanical pulp. In addition to high production pulp fibers, the fabric may contain papermaking fibers, such as softwood fibers and / or hardwood fibers. In one embodiment, the fabric is made entirely of high production pulp fibers and soft wood fibers. The softwood fibers may be present in an amount from about 95% to about 70% by weight.
With reference to Figure 2, a method is shown to make continuously dried sheets of paper in accordance with this invention. (For simplicity, the various tension rollers used to define the various fabric runs are shown but not numbered. It will be appreciated that variations of the apparatus and method illustrated in Figure 2 can be made without departing from the scope of the invention). A double wire former is shown having a main box for making paper in layers 10 which injects or deposits a jet 11 of an aqueous suspension of fibers for making paper in the forming fabric 13 which serves to support and transport the newly formed fabric down in the process as the fabric is partially dewatered to a consistency of about 10 percent by dry weight. Additional drainage of wet tissue can be performed, such as by vacuum suction, while the wet fabric is supported by the forming fabric.
The wet fabric is then transferred from a forming fabric to a transfer fabric 17 which moves at a slower speed than the forming fabric in order to impart increased stretch in the fabric. This is commonly referred to as a "hasty" transfer. Preferably the transfer fabric can have a vacuum volume that is equal to or less than that of the forming fabric. The relative speed difference between the two fabrics can be from 0-60 percent, more specifically from about 10-40 percent. The transfer is preferably carried out with the assistance of a vacuum shoe 18 in such a way that the forming fabric and the transfer fabric simultaneously converge and diverge at the leading edge of the vacuum groove.
The fabric is then transferred from a transfer fabric to the drying cloth in a continuous fashion 19 with the aid of a vacuum transfer roller 20 or a vacuum transfer shoe, optionally again using a fixed aperture transfer as previously described. he described. The continuous drying fabric can be moved at about the same speed or at different speeds relative to the transfer fabric. If desired, the continuous drying fabric can run at a slower speed for a further enhanced stretch. The transfer is preferably performed with vacuum assistance to ensure the deformation of the sheet to conform to the drying fabric continuously, thus producing the desired volume and appearance.
In one embodiment, the continuous drying fabric contains high and long print knuckles. For example, the continuous drying fabric may have about 5 to about 300 printing knuckles per square inch that are lifted at least about 0.005 inches above the plane of the fabric. During drying, the fabric is microscopically arranged to conform to the surface of the drying fabric continuously.
The level of vacuum used for tissue transfer can be from about 3 to about 15 inches of mercury (75 to about 380 millimeters of mercury), preferably about 5 inches (125 millimeters) of mercury. The vacuum shoe (negative pressure) can be replaced or replaced by the use of positive pressure from the opposite side of the fabric to blow the fabric into the next fabric in addition to or as a replacement to suck it into the next vacuum fabric. Also, a vacuum roller or rollers can be used to replace the shoe under vacuum.
While supported by the drying fabric continuously, the fabric is finally dried to a consistency of about 94 percent or greater by the dryer in continuous form 21 and then transferred to a transport fabric 22. The dried base sheet 34 is conveyed to the spool 24 using a transport fabric 22 and an optional transport fabric 25. An optional pressurized tumbling roller 26 can be used to facilitate the transfer of the fabric from the transport fabric 22 to the fabric 25. Suitable transport fabrics for this purpose they are Albano Internacional 84M or 94M and Asten 959 or 937, all of which are relatively soft fabrics that have a fine pattern. Even when not shown, the calender roll or the subsequent off-line calendering can be used to improve the softness and smoothness of the base sheet 34.
In order to improve wet flexibility, the paper fabric may contain wet flexible fibers, such as high production fibers, as described above. High production fibers include, for example, thermomechanical pulp, such as bleached chromo-thermo-mechanical pulp (BCT &P). The amount of high production pulp fibers present in the sheet may vary depending on the particular application. For example, high production fibers may be present in an amount of about 5 percent by weight or greater, or specifically about 15 percent by weight or greater, and even more specifically from about 15 to about 30. %. In other embodiments, the percentage of high production fibers in the fabric may be greater than any of the following: about 30%, about 50%, about 60%, about 70%, and about 90%.
In one embodiment, the non-creped continuous dried fabric can be formed from multiple layers of a fiber supply. Both the strength and the softness are achieved through the layering of the fabrics, such as those produced in stratified main boxes where at least one layer supplied by the main box comprises soft wood fibers while another layer comprises fibers of another type or hard wood. Layered structures produced by any means known in the art are within the scope of the present invention.
In one embodiment, for example, a layered or layered fabric is formed containing pulp fibers of high production in the center. Because high production pulp fibers are generally less smooth than other papermaking fibers, in some applications it is advantageous to incorporate them into half the tissue of the paper, such as being placed in the center of a sheet in three layers . The outer layers of the sheet can then be made of soft wood fibers and / or hardwood fibers.
In addition to containing high production fibers, the paper web may also contain a wet strength agent to improve wet flexibility. In fact, the combination of non-compressible drying for molding a three-dimensional tissue paper, coupled with wet strength additives and applying wet flexible fibers produce fabrics that maintain a usually high volume when wet, even after being compressed.
"Wet strength agents" are materials used to immobilize the bonds between the fibers and the wet state. Any material that when added to a paper or sheet fabric results in providing the sheet with either tensile strength ratio of wet geometric medium to dry geometric tensile strength in excess of 0.1 (the ratio of wet to dry traction) , or a dry traction wet traction ratio in the transverse direction in excess of 0.1 (wet to dry ratio in the transverse direction), for purposes of this invention, will be referred to as a wet strength agent. Typically, these materials are referred to either as permanent wet strength agents or as "temporary" wet strength agents. For the purposes of temporary wet strength differences, the permanent will be defined as those resins that, when incorporated into tissue or paper products, will provide a product that retains more than 50% of its original wet strength after exposure to water for a period of at least five minutes. Temporary wet strength agents are those that show less than 50% of their original wet strength after being saturated with water for five minutes. Both kinds of material find application in the present invention, even when permanent wet strength agents are believed to offer advantages when a pad of the present invention will be used in a wet state for a prolonged period of time.
The amount of wet strength agent added to the pulp fibers can be at least about 0.1 percent by dry weight, more specifically about 0.2 percent by dry weight or greater, and even more specifically from about 0.1 percent by dry weight. about 3 percent by dry weight based on the dry weight of the fibers.
The permanent wet strength agents will provide a more or less long term wet flexibility to the structure. In contrast, temporary wet strength agents can provide structures that have low density and high flexibility, but may not provide a structure that has long term resistance to water exposure. The mechanism by which the wet strength is generated has little influence on the products of this invention while the essential property of generating the water resistant bond at the fiber / fiber bonding points is obtained.
Suitable wet strength permanent agents are typically water soluble, cationic oligomeric or polymeric resins which are capable of being bonded in the form. crossed with themselves (crosslinked homo-linked) or with cellulose or other constituent of wood fiber. The most widely used materials for this purpose are the class of polymer known as polyamide-polyamine-epichlorohydrin (PAE) type resins. Examples of these materials have been sold by Hercules, Inc., of Wilmington, Delaware, as KYMENE 557H. Related materials are marketed by Henkel Chemical Co., of Charlotte, North Carolina and by Georgia-Pacific Resins, Inc., of Atlanta, Georgia.
Polyamide-epichlorohydrin resins are also useful as binder resins in this invention. Materials developed by Monsanto and sold under the SANTO RES label are activated base polyamide-epichlorohydrin resins that can be used in the present invention. Although not commonly used in consumer products, polyethylene imine resins are also suitable for immobilizing binding sites in the products of this invention. Another class of wet strength agents of the permanent type is exemplified by the aminoplast resins obtained by the reaction of formaldehyde with melamine or urea.
Suitable temporary wet strength resins include, but are not limited to, those resins that have been developed by American Cyanamid and are sold under the name of PAREZ 631 NC (now available from Cytec Industries, West Paterson, New Jersey). Other temporary wet strength agents that may find application in this invention include modified starches such as those available from National Starch and sold as CO-BOND 1000. With respect to the classes and types of wet strength resins listed, it should be understood that this list is merely to provide examples and that this does not mean excluding other types of wet strength resins, nor does it mean limiting the scope of this invention.
Although wet strength agents as described above find particular advantage to use in connection with this invention, other types of binding agents can also be used to provide the necessary wet flexibility. They can be applied to the wet end of the manufacturing process of the base sheet or applied by spraying or printing, etc., after the base sheet is formed or after drying.
Wet and dry tensile strengths of the absorbent layer can be measured with a universal testing machine device such as an Instron apparatus, and use a crosshead speed of 10 inches per minute with a length of 4 inches in gauge and a width of 3 inches of jaw under the standard conditions of the Technical Association of the Pulp and Paper Industry (TAPPI) (samples conditioned 4 hours at 50% relative humidity and 73 degrees Fahrenheit). The dry tensile strength (taken either in the machine direction, the transverse direction, or the geometric means of the directions to the machine and transverse) of the absorbent layer can be any of the following: 500 grams by 3 inches or greater, about 1000 grams per 3 inches or greater, about 1500 grams per 3 inches or greater, about 2000 grams per 3 inches or greater, about 2500 grams per 3 inches or greater, and about 3000 grams per 3 inches or greater, such as from about 800 grams per 3 inches to about 3000 grams per 3 inches. The wet tensile strength (taken either in the machine direction, the transverse direction, or the geometric means of the directions to the machine and transverse) of the absorbent layer can be any of the following: about 200 grams per 3 inches or greater, about 500 grams per 3 inches or greater, about 700 grams per 3 inches or greater, about 800 grams per 3 inches or greater, about 1000 grams per 3 inches or greater, about 1500 grams per 3 inches or greater , and about 2000 grams per 3 inches or greater, such as from about 500 grams per 3 inches to about 2500 grams per 3 inches. Optionally, the absorbent layer of the present invention may include a multilayer paper web, formed of two or more similar or different paper layers. It may be necessary, however, when a multi-layer absorbent layer is formed, to provide a secure coupling between the layers to ensure good performance of the product under expected conditions. For example, an adhesive such as a hot melt adhesive or other known secure coupling means can be used to securely bind the separated layers together to form the absorbent layer of the scrub pad. Hot melt adhesive examples may include, without limitation, hot melts of ethyl vinyl acetate (EVA) (for example, ethyl vinyl acetate (EVA) copolymers), hot melt polyolefin, hot melt polyamide, melted hot pressure sensitive, styrene-isoprene-styrene copolymers (SIS), styrene-butadiene-styrene copolymers (SBS), ethylene ethyl acrylate copolymers (EEA); hot melts of reactive polyurethane (PUR), and the like. In one embodiment, poly (alkyloxazoline) hot melt compounds can be used. Isocyanates, epoxies, and other known adhesives can also be used. Specific examples of adhesives that may be suitable for some embodiments of the present invention include SUNOCO CP-1500 (an isotactic polypropylene) from Sunoco Chemicals (of Philadelphia, Pennsylvania); Eastman CIO, Eastman C18, and Eastman P1010 (an amorphous polypropylene) from Eastman Chemical (of Longview, Texas); Findley H1296 and Findley H2525A from Elf Atochem North America (from Philadelphia, Pennsylvania); HM-0727, HM-2835Y, and 8151-XZP from H.B. Fuller Company (of St. Paul, Minnesota); and National Starch 34-1214 and other adhesives from the National Starch series 34, made from National Starch & Chemical Corp., (of Berkeley, California).
When the adhesive compound (including but not limited to hot melt materials) is used to bond tissue layers or to bond the tissue layer to an abrasive tissue, the adhesive may be able to bind to the tissue at a temperature greater than 110 degrees. centigrade, greater than 140 degrees centigrade, or greater than 155 degrees centigrade, such as from about 110 degrees centigrade to about 200 degrees centigrade, or from 135 degrees centigrade to 185 degrees centigrade. Hot melt adhesives generally comprise of a resistance imparting polymer, a glutinizing resin, a plasticizer, and optional components such as antioxidants. The adhesive compound may comprise a plasticizer, such as about 10% or more of plasticizer by weight, or less than about 30% plasticizer by weight, and more specifically less than about 25% plasticizer by weight. The glutinizing resin likewise constitutes about 10% by weight or greater of the mass of the adhesive, or less than about 25% by weight or less than about 15% by weight of the adhesive.
In one embodiment, the adhesive material may be a bicomponent fiber disposed between two adjacent layers such as a bicomponent sheath and core fiber. In addition to conventional bicomponent binding fibers, a fiber comprising two different varieties of polylactic acid can be used, so that the polylactic acid can have melting points in the range from about 120 degrees centigrade to 175 degrees centigrade, allowing a form with a High point cast to serve as a core with a variety of low melted point that serves as the sheath.
The latex materials can also serve as the adhesive joining two layers in the product of the present invention. Examples of latex adhesives include the latex 8085 from Findley Adhesives. In some embodiments, the product is substantially latex free or may have less than 10 weight percent latex, more specifically less than 5 weight percent latex, and more specifically about 2 weight percent latex or less. The latex referred to for any purpose in the present specification can be any latex, synthetic latex (for example, a cationic or anionic latex), or natural latex or derivatives thereof.
When hot melt is used as a binder material to join adjacent layers of the material, any known device for hot melt application can be used, including blown blow devices, ink jet printheads, spray nozzles, and holes Pressurized The nozzles or other means may be used to apply the adhesive in a random or non-random pattern, such as a spiral pattern, or other patterns. The diameter of the nozzle can be from about 0.1 millimeters to 2 millimeters, more specifically from about 0.2 millimeters to about 0.6 millimeters, or from 0.65 millimeters to 1.75 millimeters. Alternatively, the diameter of the nozzle may be greater than 0.3 millimeters or greater than 0.6 millimeters.
Other systems for applying adhesive to join layers include systems for applying continuous jets of a hot melt adhesive in a distinctive pattern to a substrate. The method includes a gas steering mechanism for forming a plurality of gas jets arranged to draw jets of material to impart a vortex motion to each of the jets of material as they move toward the substrate. Semi-cyclic patterns of the adhesive on the substrate are achieved while controlling a selected placement in the transverse direction of one or more of the deposited patterns. In addition to the semi-cycloid patterns, any known hot melt pattern can be applied as a continuous or pulse or discontinuous spray to a tissue or non-woven layer to form a laminate according to the present invention. Other standard specimens include deposits in the form of omega, sinusoidal deposits, straight lines, zigzag lines or sawtooth, or top hat patterns, or combinations thereof. The adhesives can also be applied in an open pattern web of adhesive filaments as is generally known in the art.
Each individual absorbent layer can have an Air Permeability value greater than 30 cubic feet per minute (CFM), such as around 40 cubic feet per minute (CFM) or greater, of around 60 cubic feet per minute (CFM) or greater, and around 80 cubic feet per minute (CFM) or greater. Alternatively, the absorbent layer may have an Air Permeability of between about 15 and 30 cubic feet per minute (CFM), or from about 20 cubic feet per minute (CFM) to about 80 cubic feet per minute (CFM). Higher values are also possible. For example, the Air Permeability of the absorbent layer may be around 150 cubic feet per minute (CFM) or greater, 200 cubic feet per minute (CFM) or greater, 300 cubic feet per minute (CFM) or greater, or 400 cubic feet per minute (CFM) or greater. By way of example, the tissue continuously dried by uncreped air comprising high production fibers has been measured to be 615 cubic feet per minute (CFM), in a fabric of 20 grams per square meter; a sample of the Scott® towel (from Kimberly-Clark Corp., of Dallas, Texas) was measured to have a permeability of 140 cubic feet per minute (CFM); A sample of the VIVA® paper towel (from Kimberly-Clark Corp., of Dallas, Texas was measured having a permeability of 113 cubic feet per minute (CFM).
A dry scouring product comprising an abrasive structure and an absorbent layer need not be substantially permeable to gas, but nevertheless may have an Air Permeability of any of the following: about 10 cubic feet per minute (CFM) or greater, about 50 cubic feet per minute (CFM) or greater, around 80 cubic feet per minute (CFM) or greater, around 100 cubic feet per minute (CFM) or greater, or around 200 cubic feet per minute (CFM) or greater, around 300 cubic feet per minute (CFM) or greater, and around 350 cubic feet per minute (CFM) or greater, such as from about 10 cubic feet per minute (CFM) to about 500 cubic feet per minute (CFM), or from around 20 cubic feet per minute (CFM) to around 350 cubic feet per minute (CFM), or from around 30 cubic feet per minute (CFM) to about 250 cubic feet per minute (CFM), or from around 40 pi is cubic per minute (CFM) to around 400 cubic feet per minute (CFM).
The abrasive structure and the absorbent layer can be combined to form the scouring pad of the present invention by any suitable method. Figure 3 illustrates a possible method of combining the layers wherein a meltblown layer 32 is formed directly on the paper web 34 in the forming machine 110. In this embodiment, it may be desirable to reinforce the bond between the layers beyond of which they are formed when the polymer solidifies in the tissue. For example, an adhesive can be applied to the paper fabric 34 prior to the deposition of the melt blowing layer 32 on the paper web 34. The adhesive can then help to adhere the layers of the scrubbing pad together. Alternatively, after the formation of the meltblown layer 32 in the paper fabric 34, heat and optionally pressure can be applied to the composite product to melt the layers together by a thermal bonding process. For example, the composite product can be heated to a temperature to soften the fibers of the meltblown layer so as to develop a degree of penetration of a portion of the polymer into the paper tissue's viewing surface to create a strong and durable bond between the layers.
In an embodiment such as that illustrated in Figure 3, it may be desirable to maintain a high meltblown temperature as it hits the tissue such that the meltblown material can bond with the fibers of the tissue layer. Without wanting to be tied to the theory, it is believed that for good adhesion of the meltblown layer to the tissue during use, for example, when the laminate is wet and subject to scouring action, a part of the meltblown material may become entangled with the fibers of the tissue or may have penetrated within the porous matrix of the tissue tissue sufficient to prevent delamination of the blown layer with fusion of the tissue when the tissue is moistened. Achieving such results can be done through the use of heated air to blow the melt from the meltblowing spinners to the tissue, and / or using the vacuum under the tissue to pull a portion of the material viscous blown with fusion in the porous matrix of the tissue of the tissue. For example, the vacuum can be applied in the forming zone to help pull the polymer fibers in the fabric for better binding and possible entanglement with the cellulose fibers. When the vacuum is used, however, care must be taken to prevent excessive airflow in the vicinity of the tissue which may solidify the meltblown fibers before contacting the tissue. Narrow vacuum boxes, controlled air flow rates, pulsed vacuum, and other means, optionally coupled with radioactive heating or other means of temperature control of materials or fluids (eg, air), can be used by those with skill in the art to optimize the bond between the abrasive layer and the absorbent layer.
In one embodiment, the cellulose fabric may be preheated or heated as the polymer fibers are deposited therein (either by meltblowing or spinning directly onto the cellulose fabric, or by bonding to a layer previously formed from polymeric fibers to cellulose tissue). For example, an infrared lamp or other heating source can be used to heat the cellulose fabric in the vicinity where the polymer fibers contact the cellulose fabric. By heating the surface of the cellulose fabric, better bonding between the cellulose fabric and the polymer fibers can be achieved, especially when the fibers are newly formed, cooled meltblown fibers. A combination of heating and suctioning down the cellulose fabric can be useful, and either or both of these operations can also be combined with mechanical pressure (e.g., point bonding, roll pressure, stamping, etc.) for further bonding of the fibers polymeric to the cellulose tissue.
Alternatively, the paper web and the abrasive layer of the scrubbing pad can be separately formed, and then coupled after, after forming. For example, as illustrated in Figure 4, the paper web 34 and the meltblown fabric 32 can be guided together with guide rollers 102 and 104, and brought into contact between the roller 100 and the roller 80.
When an abrasive layer containing thermoplastic has been previously formed and is no longer hot enough to readily attach to the absorbent layer, the heat can be applied to cause bonding of the abrasive layer with the absorbent layer as the two are contacted or after that the two are contacted. For example, the absorbent layer may be sufficiently preheated to cause partial melting of the abrasive layer as it touches the tissue paper, optionally with the assistance of mechanical compression. Alternatively, the heat can be applied to the tissue and / or the abrasive layer after the two have been brought into contact to cause at least partial melting of the blown layer with melt with the absorbent layer. The heat can be applied conductively, such as by contacting the tissue layer against the heated surface which heats the tissue sufficiently to cause fusing of the parts of the abrasive layer in contact with the tissue, preferably without much heating of the polymeric layer . Radioactive heating, heated by radio frequency (for example heated by microwave), heated inductive, heated convector with heated air, jet, or other fluids, and the like, can be applied to heat the tissue layer and the polymer layer while it is in contact one another, or to independently heat either layer before joining the other.
Ultrasonic bonding and pattern bonding can also be applied. For example, a rotary horn activated by ultrasonic energy can compress parts of the abrasive layer against tissue tissue and cause the melting of parts of the polymeric layer due to the welding effect driven by the ultrasound. Likewise, a heated pattern plate or drum can compress parts of the abrasive layer in contact with the tissue in the compressed portions, so that a good coupling of the compressed parts to the tissue tissue can be achieved. Several different patterns can be used in joining the layers together. For example, in an embodiment, only the edges of the layers are joined. In other embodiments, several other patterns are used that extend uniformly or non-uniformly across the surface of the layers.
In an alternative embodiment, as shown in Figure 5, the layers of the present invention can be put together after forming, and an adhesive 82 can be applied to one or both layers of the pad before contacting which can bind the layers of the pad together. In this incorporation, the layers can be coupled through the use of the adhesive alone, or optionally, the heat and / or pressure can also be applied after the layers are joined, for further improved bonding between the layers. An adhesive can be applied to one or both layers of the scrub pad by any method. For example, in addition to a spray method, as illustrated in Figure 5, an adhesive may be applied through any known method, printing, coating, or other suitable transfer method. In addition, the adhesive can be any suitable adhesive that can firmly bond the layers of the pad together. The basis weight of the adhesive can be about 5 grams per square meter (gsm) or greater, such as from about 10 grams per square meter (gsm) to about 50 grams per square meter (gsm), more specifically around of 15 grams per square meter (gsm) to around 40 grams per square meter (gsm).
Alternatively, the basis weight of the added adhesive can be less than about 5 grams per square meter (gsm).
The most suitable method for joining the layers of the pad to scrubbing together may depend at least in part on the textures of the layers. As previously described, the melt blown layer and / or the paper fabric can be formed on relatively smooth forming surfaces and thus exhibit little three dimensional surface texture, or alternatively, one or both of the layers can be formed on surfaces highly textured. For example, Figure 7 illustrates the cross section of a scouring pad 30 formed of an abrasive layer 32 attached to a paper web 34, both of which have relatively smooth surface textures. In such incorporation, any of a number of methods can be used to join the layers together including methods involving adhesives, heat, pressure, or any combination thereof.
In an alternative embodiment, one or both of the layers may exhibit a high degree of surface texture. For example, as illustrated in Figure 8, the meltblown layer 32 may be a highly textured meltblown layer and a paper web 34 may be relatively flat. In such incorporation, a method for joining knit may be preferred to firmly bond the layers to those points where the meltblown layer 32 and the paper fabric 34 contact while maintaining the texture of the meltblown layer 32. Any of a A variety of well-known spot joining methods can be used, including those methods involving various adhesives and / or heat, without subjecting the composite structure to excessive pressure which can damage the texture of the meltblown layer 34. Of course, the pad for scrubbing can optionally be formed of a highly textured paper fabric attached to a relatively flat abrasive layer. Alternatively, both layers can be highly textured, and may have the same or different texturing patterns.
A variety of alternative methods can also be used to join two or more layers of tissue, or a layer of tissue to an abrasive layer. These methods include, but are not limited to: • Add non-tacky binder fibers between two adjacent layers, and subsequently apply heat (e.g., infrared radiation, heated air, contact with heated surface, inductive heat, microwave radiation, and the like) to cause at least partial melting of the binder fibers to join the adjacent layers. The layers may be substantially uncompressed or may be subjected to mechanical compression during or after heating while the binder fibers are still sufficiently hot to be capable of bonding. When mechanical compression is used to facilitate bonding, the applied mechanical loads are less than any of the following: 100 kPa, 50 kPa, 25 kPa 10 kPa, 5 kPa, 1 kPa, or loads of between about 1 kPa and 20 kPa, or between 10 10 kPa, and 50 kPa.
• Apply a hot melt sticky material to one or more layers before contacting an adjacent layer. He Hot melt can be in the form of meltblown fibers entrained in hot air to prevent premature tempering, or hot melt material sufficiently heated that it can remain tacky after contacting the layer to which it is applied, after the second layer is brought into contact with the hot melt material in the first layer to cause bonding of the two layers. layers. A possible method for laminating two layers includes meltblown fibers injected through a blown head with melting between two layers supported on opposite suction rollers that do not join the layers together, followed by a calender roll or engraving roller that does not Press the layers together to cause bonding.
• Extrusion of thermoplastic or foam sticky polymer between the two layers, such as a foam precursor fused with blowing agents that expand after extrusion to create a porous structure in the foam. The foam can be an open cell foam with pores sized per size sufficiently small (eg, less than 1 millimeter, such as from about 10 microns to 50 microns) to cause the generation of foam when a cleaning cloth comprises of the foam used with soapy water or water containing other cleansing agents capable of foaming, wherein the product is squeezed while is wet with cleaning solution generates foam as the solution is forced through the absorbent layer, as is often the case using conventional sponges. However, only a thin layer of foam may be needed to achieve both the binding effect and the foam generating effect when used with certain cleaning solutions. The foam layer may have a thickness of less than 8 millimeters, such as from about 10 millimeters to 6 millimeters, or from 1 millimeter to 3 millimeters, and may have a basis weight of less than 10 grams per square meter (gsm) ) or less than 5 grams per square meter (gsm), even though 15 higher weights may be used, such as 10 grams per square meter (gsm) or greater, 30 grams per square meter (gsm) or greater, or around 40 grams per square meter (gsm) or greater, with 20 specimens ranges from around 15 grams per square meter to around 60 grams per square meter or from around 20 grams per square meter to around 60 grams per square meter. In one embodiment, a foam layer may be on both sides of the absorbent layer, for example between the two main layers of the scrubbing pad and on the outer surface of the absorbent layer.
Mechanical bonding can also be used, including stitching or crimping of adjacent layers to create mechanical entanglement of the fibers. However, some degree of bonding by adhesive may still be needed for better results.
• The application of binder materials other than thermoplastic binders to join adjacent layers. Such binder materials may include pressure sensitive adhesives; curable adhesives such as glues; salt-sensitive binders that are effective in the presence of a solution containing salt.
The scouring pad compound of the present invention will both include an abrasive layer and an absorbent layer which are usually directly coupled to each other, although in certain embodiments an additional layer can be included between the two main layers.
Figure 9 illustrates another embodiment of the scouring pad wherein both the absorbent layer 34 and the abrasive layer 32 exhibit a high degree of three dimensional texture. In the embodiment illustrated in Figure 9, both layers have the same nested textured pattern. Alternatively, the layers may have different texturing patterns. As with the other embodiments, only the limitation in the method of joining the two layers together is that the desired surface texture of a layer is not destroyed in the coupling method. For example, when the two layers exhibit different overlapping texturing patterns, a point joining method may be preferred.
In an embodiment, such as, that illustrated in Figure 9, the texture of the surface in one of the layers can be formed when the two layers are coupled together. For example, the absorbent layer 34 can be a highly textured fibrous cellulose fabric such as a non-creped continuous dried paper web, and the abrasive layer 32 can be formed on or bonded to the absorbent layer and can conform to the textured pattern. of the absorbent layer while the two layers are combined. For example, heat can be applied to the article of the compound as a part of the bonding process. This can cause the abrasive layer to soften and take on the textured pattern of the absorbent layer, and the absorbent layer can continue to exhibit the same textured pattern as the absorbent layer after the layers are coupled together.
Increasing the surface texture of the abrasive layer in such a way can increase the total abrasion capacity of the composite product. Therefore, a synergy can exist between the two layers, and the total abrasion of the scouring article on the abrasive surface can be greater than the abrasion capacity of any layer before coupling.
Further, in these embodiments where the absorbent layer of the fabric can exhibit a high degree of wet strength, the added texture of the abrasive layer can withstand, even after the scrubbing article has been saturated with water or some other fluid from the fabric. cleaning.
The composite scouring pad can exhibit a synergy between the layers of other modes as well. For example, the fibers of the two layers can be physically entangled or fused together in the coupling process, such that there is a fairly strong bond between the layers. In such an embodiment, the tensile strength of the composite product may be greater than the sum of the tensile strengths of the two layers before coupling, or, alternatively, greater than the tensile strength measured when the two layers are coextensively arranged adjacent to one another. to the other but not joined together, and tested together by combined tensile strength.
The composite scouring pads of the present invention can exhibit desired cleaning characteristics, such as good abrasion capacity and wet flexibility, for example, while requiring fewer raw materials and having good flexibility for easy handling. For example, in one embodiment, the scouring pads of the present invention may have a total basis weight of less than 150 grams per square meter. The scrubbing pads of the present invention may also be less than about 7 millimeters thick. More particularly, the scrubbing pads can be less than about 4 millimeters thick. The abrasive layer may have a thickness of about 0.5 millimeters or greater, as measured with the equipment used in the Thickness Variation test, or the thickness may be any of the following values: about 1 millimeter or greater, about 2 millimeters or greater, of about 3 millimeters or greater, of about 4 millimeters or greater, of about 5 millimeters or greater, such as from about 0.5 millimeters to 10 millimeters, or from about 1 millimeter to 5 millimeters. Alternatively, the thickness of the abrasive layer can be less than 3 millimeters.
Additional layers may also be included in the scouring pad of the present invention, if desired.
For example, the scouring pad of the present invention can include two abrasive layers on opposite surfaces of the pad, both coupled to one or more absorbent layers that are interspersed in the middle of the pad.
In one embodiment of the present invention, a barrier layer formed of a barrier material or size sorting agent can be included on or on each side of the absorbent layer. This can be useful when small amounts of a cleaning compound are used (eg, a furniture polish, a window washer, or a harsh agent such as an oven cleaning agent), where the moistening of the entire pad is undesirable. For example, a barrier layer may be between the absorbent layer and the abrasive layer, or, alternatively, may be on the outer surface of the absorbent layer. In one embodiment, the barrier material may be removable. For example, in an embodiment of the present invention, a barrier layer may include a waterproof barrier material on the outer surface of the absorbent layer which may allow the hand to remain dry during use.
The barrier material, in one embodiment, can be a hydrophobic film. It must be understood, however, that any suitable waterproof material can be used. For example, suitable wet barrier materials include films, fabrics, nonwovens, laminates or the like. The barrier material may be a liquid impervious fabric or a sheet of plastic film such as polyethylene, polypropylene, polyvinyl chloride or a similar material. In addition, the barrier material may occupy only a part of the surface area of the paper web or may substantially cover an entire surface of the paper web.
In addition to the paper fabric and the abrasive layer, the scouring pad of the present invention may also contain additional materials within any layer as well as additional functional layers or components. For example, a part of the pad may provide soap, detergent, waxes or polishing agents such as furniture polish, metal cleaners, leather or vinyl cleaners or restorative agents, stain removers for washing clothes, treatment solutions prior to washing, enzymatic solutions to improve fabric cleaning or conditioning, odor control agents such as active ingredients of Fabreze® odor-removing compound (Procter &Gamble, Cincinnati, Ohio), waterproof compounds, polish of shoes, dyes, glass cleaners, antimicrobial compounds, wound care agents, lotions and emollients, and the like. Other possible additives that may be added to the scrub pad include buffering agents, antimicrobials, skin care agents, such as lotions, medicaments (eg, anti-acne medicaments), or hydrophobic skin barriers, control agents of odor, surfactants, mineral oil, glycerin, and the like.
The active ingredients may be present in a solution on the cleaning cloth as it is packaged or in a solution that is added to the cleaning cloth before use. The active ingredients can also be present as a dry powder coupled to the fibers in the cleaning cloth, or as a dry compound impregnated in the fibers or in the hollow spaces between the fibers of the cleaning cloth or encapsulated in water-soluble capsules, encapsulated in wax or lipid-rich shells to allow escape with mechanical or sheath compression, or in a container coupled to or cooperatively associated with the cleaning cloth that can be opened during use or before use.
The application of the additives can be by any suitable method, such as: • Direct addition to a fibrous slurry before the formation of paper tissue. • A spray applied to a layer or to the composite pad. For example, spray nozzles can be mounted on the moving paper tissue or meltblown fabric to apply a desired dose of a solution to the layer that can be wet or substantially dry. • Printing on the fabric, such as by offset printing, recorded printing, flexographic printing, ink jet printing, digital printing of any kind, and the like. 10 • Coating on one or both surfaces, such as knife coating, air knife coating, short stay coating, mold coating, and the like. 15 • Extrusion from a matrix head of an agent in the form of a solution, a dispersion or emulsion, or a viscous mixture such as one comprising a wax, softener, debonder, oil, composed of polysiloxane, or other silicon agent, an emollient, a lotion, an ink, or other additive. • Application to individualized fibers. For example, before depositing on the As the forming surface, the meltblown fibers can be entrained in an air jet combined with an aerosol or spray of the composite to treat the individual fibers prior to incorporation into the meltblown layer. 5 • Impregnate wet or dry paper tissue with a solution or slurry, where the compound penetrates a significant distance in the thickness of the fabric, such as more than 20% of the thickness of the fabric, more specifically of at least about 30% and more specifically of at least about 70% of the thickness of the fabric, including completely penetrating the tissue completely to the full extent of its thickness. • Apply foam from an additive to a layer (for example, foam finishing), either by topical application or by impregnated the additive on the paper tissue under the influence of a differential pressure (for example, assisted vacuum impregnation of the foam). • Replenishment of a chemical agent in solution in an existing fibrous tissue. 25 • Supply of fluid in a roller of the additive for application to the fabric.
• Application of the agent by spraying or other means to a moving web or cloth that in turn contacts the layer to apply the chemical to the layer.
The level of application of an additive can generally be from about 0.1 percent by weight to about 10 percent by weight of solids relative to the dry mass of the layer to which it is applied. More specifically, the level of application can be from about 0.1 percent by weight to about 4%, or from about 0.2 percent by weight to about 2 percent. Higher or lower application levels may also be within the scope of the present invention. In some embodiments, for example, application levels from 5% to 50% or greater can be considered.
Printing, coating, spraying, or otherwise transferring a chemical agent or compound onto one or more sides of the pad, or any layer or material in the pad can be done uniformly or heterogeneously, as in a pattern, using any known agent or compound (for example, a silicon agent, an ammonium quaternary compound, an emollient, a skin-care agent, such as aloe vera extract, an antimicrobial agent, such as citric acid, an agent of odor control, a pH control agent, a size sorting agent, a polysaccharide derivative, a wet strength agent, a dye, a fragrance, and the like). Any known method can be used for the application of such additives.
In one embodiment, the scrub pad can be provided and the desired additive compound can be maintained in a separate container or dispenser. In this embodiment, the additive can be applied to the pad by the consumer in the desired amount at the time of use.
The scrub pad layers of the present invention can be combined to form a product of any desired size or shape and suitable for any particular purpose. For example, Figure 6 illustrates an embodiment of the present invention wherein a melt blown layer 32 substantially covers the surface of a paper web 34 to form a rectangular scrub pad as it can be held in the hand during use. In such an embodiment, the scrub pad can be inverted to provide both abrasive and non-abrasive type cleaning.
Alternatively, the meltblown layer can only partially cover the surface of the paper web, creating a single scrubbing surface on the scrub pad which may have both a rough abrasive region and a soft absorbent region. Therefore, the user can control the abrasion ability of the cleaning action during cleaning by, for example, adjusting the angle of the pad or the region of the pad to which the pressure is applied and can have different levels of action of scrubbing on the same side of a single scrubbing pad.
The scouring pads of the present invention can be provided in any form or orientation. For example, the pads may be square, circular, rectangular, or the like. They can be formed into gloves, such as hand-held gloves for hand scrubbing or foot-shaped covers for the feet. The pads can be packaged and sold in either the wet or dry form, and can optionally be formed to be attached to a handle or handle to form a convenient cleaning tool such as a cleaning cloth with a rinse, a mop, a cleaning tool for cleaning toilet, a dishwashing cleansing cloth, a scrub pad, a scrubbing tool for cleaning metal, ceramic, or concrete surfaces, a polishing or sanding tool, and the like.
For example, an embodiment of the invention, as illustrated in Figure 10, shows the scouring pad of the present invention 30 shaped to engage a base 220 of a rigid gripping device. The base 220 is coupled to a handle 210 formed to comfortably hold it by a user, such as it is on a mop or a smaller hand-scrubbing device. The scrub pad 30 can be held on the base 220 by any method that can firmly hold the pad, however, in one embodiment, it can release the pad to replace it quickly and easily. For example, the pad 30 may be supported on the base 220 in the gripping slots 225. In another embodiment, the scrub pad 30 may be permanently attached to the base 220, and the entire cleaning tool 10 may be disposable.
The cleaning tool of the present invention can be used to clean or scrub very different surfaces, and can be designed for a specific use. For example, the cleaning tool may have a handle that includes a long stick and be used to clean floors, walls, ceilings, ceiling fans, light bulbs, windows and the like. In certain embodiments, such as when the cleaning tool is used to clean windows, for example, the cleaning tool may have a rinse aid, such as a rinse rubber material coupled to the surface as is generally known in the art. . In other embodiments, the abrasive layer on the cleaning tool can be used to sand or polish a surface to be cleaned.
In one embodiment, the scouring product of the present invention includes multiple abrasive structures that are configured in a stacked array. A suitable coupling structure supports the plurality of abrasive structures together. More particularly, the releasable coupling structure holds the abrasive structures together in such a way that the upper abrasive structure can be removed without the entire stack being delaminated or undone. In this way, the scrubbing product is "able to cool".
In the past, once the surface of a scrubbing product was worn, dirty or contaminated, the entire product was typically discarded. Scouring pads, however, tend to be expensive to manufacture and it is not economical to dispose of the products, especially after a single use. On the other hand, scouring products can become disgusting with dirt, grease, bacteria and other contaminants after only one or two uses. Due to its cost, however, consumers are known to retain used scrubbing products long after their useful life has ended.
In one embodiment of the present invention, a scouring product capable of cooling is provided in which the abrasive cleaning surface can be refreshed several times before the entire product needs to be discarded. In general, the scouring product capable of cooling includes multiple layers of an abrasive structure that are removable held together. In an embodiment, even when not necessary, the pile of abrasive structures may be coupled to a liquid-absorbing substrate, such as a sponge-like body.
For example, with reference to Figures 13 and 14, an embodiment of a generally capable scrubbing product 300 made in accordance with the present invention is illustrated. As shown, scouring product 300 includes a plurality of abrasive structures 330A, 330B, 330C, 330D, and 330E coupled to a liquid-absorbing substrate 310. Liquid-absorbing substrate 310 is optional and may not be needed in all incorporations. . Thus, the product may comprise multiple layers of an abrasive structure.
Each of the abrasive structures 330 includes an abrasive layer 332 coupled to a liquid absorbent layer 334. Each abrasive structure can be made in accordance with any of the embodiments described above. In an incorporation, the abrasive structure 330A includes an abrasive layer 332 made of a spunbond fabric, such as a nonwoven meltblown fabric. The absorbent layer 334, on the other hand, can be made of any suitable material. The liquid-absorbent layer 334, for example, can be a paper fabric such as a fabric continuously dried by uncreped air, a coform fabric, a hydroentangled fabric, a fabric placed by air, and the like. In addition, the liquid-absorbent layer 334 can be made from a single layer of material or can be made from multiple layers, depending on the particular application. In other embodiments, the liquid absorbent layer 334 may comprise a natural sponge, a synthetic sponge, a foam material, and the like.
In the embodiment illustrated in Figures 13 and 14, the abrasive structures 330 are held together by a plurality of stitches 314. The stitches 314 may extend only through the abrasive structures or through the entire scrubbing product. As shown, each abrasive structure 330 includes an appendix 318. As illustrated in Figure 14, when the appendix 318 is pulled the upper abrasive structure 330A can be removed from the scouring product 330 by exposing the abrasive structure 330B. Once the abrasive structure 330A is removed, the stitches 314 remain intact keeping the rest of the abrasive structures together.
Instead of or in addition to using the appendix 318, the scrubbing product 330 may use various other constructions to facilitate the removal of the abrasive structure. For example, in one embodiment, one side of the scrubbing product 330 can be without stitching making it easier to separate the layers.
In the embodiment shown in Figures 13 and 14, the stitches 314 are placed around the perimeter of each of the abrasive structures. In addition, the stitches are located in such a way that they do not pass through the abrasive layer 332, but only through the absorbent layer to the liquid 334. In this way, only the liquid-absorbent layer 334 tears out of the stitches when one pulls the stitch. Appendix 318 In one embodiment, in order to facilitate the removal of the abrasive structure 330A, the abrasive structure can be punctured where the stitches are located or on another side. Perforating the abrasive structure 330A, such as around the perimeter of the absorbent layer to the liquid 334, allows the abrasive structure 330A to be more easily removed from the scrubbing product 300.
Although the stitches 314 are shown around the perimeter of each of the abrasive structures, it should be understood that the stitches can be located on either side across the surface of the abrasive structures, while the stitches allow the removal of an abrasive structure. of the rest of the pile. For example, in other embodiments, a quilt design can be targeted on the scouring product by holding the abrasive structures together.
The yarn that is used to hold the abrasive structures together may vary depending on the particular application. In a particular embodiment, for example, an elastic yarn may be used. The elastic yarn can be, for example, a LYCRA yarn or a GLOSPAN yarn. In another embodiment, the elastic threads may be formed from a block copolymer, such as styrene-isoprene-styrene block copolymer. By using elastic threads, the threads will continue to keep the abrasive structures tightly together even when one or more of the abrasive structures has been removed.
In the embodiment illustrated in Figures 13 and 14, the scouring product includes five layers of abrasive structures coupled together. It should be understood, however, that in other embodiments more or less five layers may be desirable. For example, in other applications, only two layers of abrasive structures can be desired, while in other applications more than five abrasive structures can be coupled together.
The abrasive structures themselves may be identical or may be different from layer to layer. In one embodiment, for example, multiple abrasive structures can be coupled together having different scouring properties and characteristics. For example, a scouring product may have abrasive structures that become progressively more or less abrasive as the outer layers are removed and used. In an alternative embodiment, the scrubbing product can be constructed in such a way that the lower layers of the abrasive structures have higher wet strength than the upper layers.
As shown in the figures, the abrasive structures are coupled to an absorbent substrate for liquid 310. The liquid-absorbent substrate can be made of any suitable material having properties and characteristics of the sponge type. The absorbent substrate liquid 310 can be made, for example, of a natural sponge material or of a synthetic sponge material. For example, the liquid-absorbent substrate 310 can be made of cellulose foam, polyurethane foam, and the like.
In an alternative embodiment, the liquid-absorbent substrate 310 is made of multiple water-absorbing layers laminated together. Each of the layers can be, for example, a paper fabric, a fabric placed by air, a hydroentangled fabric, a coform fabric, and mixtures thereof. For example, in one embodiment, the liquid absorbent substrate 310 is made of a plurality of continuously dried fabrics without creping. The tissues can be adhered together using any suitable method. For example, the fabrics can be adhered together using an adhesive or they can be joined together using the stitches 314 as described above.
With reference to Figure 15, another embodiment of a mop-up product 350 made in accordance with the present invention is shown. In this embodiment, scouring product 350 includes abrasive structures 380A, 380B, 380C, 380D, and 380E. As shown, the abrasive structures are held together through the use of a hook-and-loop coupling system.
In particular, each abrasive structure includes an abrasive layer 382 comprising a plurality of hooks. The abrasive layer 382 is disposed with one or more layers of an absorbent layer to the liquid 384. In accordance with this embodiment, the hooks making the abrasive layer 382 not only provide a scrubbing surface for the scrubbing product but are also configured to attach to the back side of an adjacent abrasive structure. For example, the hooks can be constructed that readily engage a non-woven substrate. The nonwoven substrate comprising the liquid absorbent layer 384 can be, for example, a paper fabric, a coform fabric, a hydroentangled fabric, a bonded and carded fabric, a fabric placed by air, and the like.
The hooks comprising the abrasive layer 382 can be uniformly applied across the surface of the layer as shown in Figure 15. Alternatively, the hooks can be applied to the surface of the abrasive layer in a particular pattern. In yet another embodiment, the hooks may be applied non-uniformly to the surface of the abrasive layer.
In the embodiment shown in Figure 15, the stack of abrasive structures 380A, 380B, 380C, 380D, and 380E are coupled to a liquid absorbing substrate 360 comprising a plurality of liquid absorbing layers. For example, as described above, the liquid-absorbent substrate 360 can be comprised of multiple paper tissues bonded together.
With reference to Figure 16, there is shown another embodiment of a generally scouring product 400, made in accordance with the present invention. In this embodiment, scouring product 400 includes abrasive structures 430A, 430B, 430C and 430D. The abrasive structures are coupled to an absorbent substrate for liquid 410.
Similar to the embodiment shown in Figure 15, the abrasive structures 430A, 430B, 430C and 430D are coupled together using hook and loop fasteners. In this embodiment, however, each abrasive structure includes a first abrasive layer 432 made of a curl material coupled to one side of an absorbent layer to the liquid 434 and a second abrasive layer 402 comprising hooks coupled to the opposite side of the layer absorbent to the liquid 434. As illustrated, the hooks contained on the underside of the abrasive structures secure the curl material contained on an adjacent abrasive structure. This construction can provide several advantages over the embodiment shown in Figure 15. For example, the hook and loop fastening system can have greater strength in the Z direction. In addition, by having a terry material, such as a non-woven material on one side of the absorbent layer to the liquid and having a hook material on the opposite side of the layer, each abrasive structure includes two separate scrubbing surfaces. Therefore, once the top layer is removed from the scouring product, one can scrub an adjacent surface using either the terry material or the hook material. In addition, in this embodiment, the hook and loop system can allow the re-coupling of the layers that were previously removed.
In the embodiment illustrated in Figure 16, the curl material is shown as the upper surface of the abrasive structures while the hooks are shown on the underside of each of the abrasive structures. It should be understood, however, that a contrary construction can work equally well.
With reference to Figures 17 and 19, a further embodiment of a scouring product generally made in accordance with the present invention is shown. In this embodiment, scouring product 450 includes abrasive structures 480A, 480B, 480C, and 480D coupled to a liquid-absorbent substrate 460. Each of the abrasive structures includes an abrasive layer 482 adhered to a liquid-absorbing layer 484. In This incorporation, the abrasive structures are releasably coupled through junction points 452. These points of attachment can be made in any suitable way.
For example, in one embodiment, the bonding points 452 are created through the use of an adhesive. The adhesive may be, for example, a starch adhesive, a hot melt adhesive, or any other suitable adhesive material. The adhesive can be applied to the abrasive structures by printing, spraying or through the use of an extruder.
In an alternative embodiment, instead of using an adhesive, the bonding points 452 can be areas where the abrasive structures have been thermally bonded or joined together ultrasonically. For example, the abrasive structures can be joined together by thermal point when supplied through a heated etching device.
When the bonding points 452 are created through thermal bonding, each abrasive structure includes a sufficient amount of synthetic material for the bonding point to occur. For example, if the abrasive layer 482 is made of a spunbond fabric, the spunbond fabric can be melted and fused to an adjacent layer at the location of the bond points. In an alternative embodiment, however, the liquid absorbing layer 484 can be made with relatively high amounts of synthetic polymeric materials. For example, in this embodiment, the liquid absorbent layer 484 may be a coform fabric, an air-laid fabric, or a hydroentangled fabric containing a sufficient amount of thermoplastic polymer material for the junction point to occur when the multiple layers be recorded together.
In the embodiment shown in Figure 17, the attachment points 452 are shown on the perimeter of the abrasive structures. In the embodiment shown in Figure 19, however, the attachment points 452 are uniformly applied on the surface of the abrasive structures. In general, a sufficient number of attachment points 452 should be present in a sufficient density to maintain the multiple layers of the abrasive structures together during use. The number and spacing of the attachment points 452, however, must also be such that an abrasive structure can be removed from an adjacent abrasive structure when desired.
With reference to Figure 18, another embodiment of a scrubbing product 500 made in accordance with the present invention is illustrated. In this embodiment, scouring product 500 includes abrasive structures 530A, 530B, 530C, 530D and 530E. The stacked abrasive structures are coupled to an absorbent substrate 510 which, in this embodiment, is made of multiple layers. As shown, each abrasive structure includes an abrasive layer 532 coupled to an absorbent layer 534.
In order to connect the multiple abrasive structures together, in this embodiment, the scrubbing product 500 includes a plurality of openings 514. The placement of openings through the abrasive structures increases the resistance in the Z-direction of the product. The openings 514 can be located along the perimeter of the scouring product 500 as shown can be evenly distributed across the surface of the scouring product.
The openings may extend only through the abrasive structures 530 as shown in Figure 18 or may extend only through the absorbent substrate of the liquid 510.
The diameter of the openings may vary depending on the particular application. For most incorporations, however, the openings can have a size of less than about 5 millimeters, particularly of less than about 3 millimeters. In one embodiment, an additive as described above may be contained in the openings which is subsequently released when the scrubbing product is wetted. For example, the openings may contain a soap or a detergent.
In general, the different fastening structures described above in Figures 13-19 can be used alone or in a combination. For example, the openings 514 as shown in Figure 18 may be very suitable in some embodiments to be combined with the knit joints or the stitches.
The general shape of the product can also vary depending on the particular application. The product may, for example, be in the form of an oval as shown in the figures, or it may be in the form of a rectangle. Referring to Fig. 20, another embodiment of a scouring product 550 made from steel with the present invention is still shown. As illustrated, in this embodiment, the scouring product has been made in the shape of a fish.
Another embodiment of a scouring product generally 552 is shown in Figure 21. In this embodiment, the abrasive structures 554A, 554B, %% C, 554D and 554E are all interconnected along the perforation lines 556. In this incorporation, in addition to a fastening structure such as any of the fastening structures described in Figures 13-19, the abrasive structures are also interconnected together through the use of perforation lines. By interconnecting the absorbent structures together, not only can the manufacture of the product be facilitated, but the overall integrity of the product can also be somewhat improved.
Referring to Figure 22, yet another embodiment of a generally refreshable multilayer scrubbing product 600 is shown. In this embodiment, a plurality of abrasive structures 630A, 630B and 630C completely surround and envelop a water-absorbent substrate 610. Each abrasive structure includes an abrasive layer 632 and an absorbent fabric 634. In this embodiment, the abrasive structures used can be removed. of the product to scrub one at a time such as by peeling the layers of an onion.
More particularly, each of the abrasive structures 530 includes a perforation line 602. Once a user wishes to have an outer abrasive structure, the user tears the perforation line 602 to remove the outermost layer.
In this embodiment, the use of a clamping structure to retain the individual abrasive structures together may not be required. Various clamping structures can be used as described above.
Referring to Fig. 23, a multi-layered scouring product 700 having a generally cylindrical shape is generally shown. As illustrated, scouring product 700 includes a liquid-absorbing substrate 710 surrounded by layers of an abrasive structure 730. Each abrasive structure includes an abrasive layer 732 placed on a carrier layer 734. Similar to the embodiments shown in the figure 22, the scouring product 700 includes drilling lines 702 that are used to remove the outermost abrasive structure.
In another embodiment shown in Figure 23, multiple abrasive structures may be included that are either spirally wound around the liquid absorbent substrate 710 or alternatively are individually wrapped around each other much like the embodiment shown in Figure 22.
In the embodiment shown in Figure 23, a liquid absorbing or core 710 substrate may not be necessary. In other embodiments, the scrubbing product 710 may be coreless or may contain a rigid substrate that is not water absorbent.
Test Methods "Gurley stiffness" refers to stiffness measurements of a fabric made with a Gurley ™ 9109 bending strength tester, model 4171-D (Precision Instruments, Troy, New York). The tests are done with conditioned samples for at least four under TAPPI conditions (50% relative humidity at 23 ° C). An appropriate method for determining Gurley stiffness values follows as established in the TAPPI 543 OM-94 standard T test, but modified to use 1.5-inch sample lengths instead of two inches, and 1.0-inch sample widths instead. of 2 inches. Using a 1-inch-wide sample that is 1.5 inches long, the formula for converting the Gurley reading to a Gurley stiffness with milligram units is: Rigidity = Gurley reading * 11.1 mg * (inches from center / 1 inch) * (weight / 5 g).
Therefore, a Gurley reading of 8 taken when a weight of 25 grams 2 inches was used from the center would be converted to a stiffness of 8 * 11.1 mg * 2 * (25 g / 5 g) = 888 mg.
The abrasive layers of the present invention and / or the laminates of the present invention and / or the laminates of the present invention may have a Gurley stiffness of about 2500 mg or less, specifically about 1500 mg or less, more specifically about 800 mg or less, more specifically still about 400 mg or less, and more specifically about 200 mg or less, such as from about 40 mg to 350 mg or from about 80 mg to about of 400 mg. These stiffness values can be a maximum value obtained by the measurements in any direction of the woven product (maximum rigidity) or in the machine direction or in the transverse direction (respectively MD or CD stiffness).
The "variation in thickness" refers to the non-uniformity of the thickness of an abrasive layer. The measurement involves taking spaced and separated measurements of sample thicknesses with a TMI model 49-62 precision micrometer (Testing Machines, Inc., of Amityville, New York) having a foot of 0.63 inches in diameter that applies a pressure of 7.3 pounds per square inch (50 kPa). The test is done after the instrument was heated for one hour and is done under the standard TAPPI conditions. The strips of material to be tested are measured at points on 1-inch centers to provide multiple measurements per strip. At least three strips of material are used and at least 9 readings per strip are taken. The thickness variation is a standard deviation of the thickness results, reported in millimeters.
"Wet opacity" and "dry opacity" refers to measurements of the optical opacity of a sample in the dry or wet state, respectively using a Technibritemarca Micro TB-1C device (from Technidyne Corporation, New Albany, Indiana), according to the manufacturer's instructions for ISO opacity, with the test made for samples with the abrasive layer facing up. The test is done under standard TAPPI conditions. The wet opacity is then measured at an opacity of a sample that has been wetted by immersing it and saturating the sample for one minute in demonized water at 23 ° C. The sample is then removed from the water, holding it at a corner to allow drainage of excess water to drain for three seconds. The sample is then placed on a dry blotting paper for 20 seconds, then turned over and placed on another dry blotter and allowed to settle for another 20 seconds, and then immediately tested for opacity.
In some embodiments, the articles of the present invention may have a relatively low wet opacity, so that the user can observe the presence of points or other objects through the wet article during cleaning. Conventional sponges and other cleaning articles tend to be essentially opaque, but the translucent nature of the articles in some embodiments of the present invention may be of use in some cleaning situations. Therefore, the articles of the present invention may have a lower wet opacity of around any of the following: 95%, 90%, 80%, 70%, 60%, 50%, and 40%, with each of the example ranges from 30% to 95%, or from 50% to 90% or from 40% to 80%. The dry opacity may be greater than 96%, such as about 100%, or it may be less than 96%, such as from 80% to about 95%, or from 50% to 90%, or from 40% to 85%. In one embodiment, the difference between the dry opacity and the wet opacity of the article can be at least about 10%.
The "global surface depth". A three-dimensional base fabric or sheet is a sheet with a significant variation in surface elevation due to the intrinsic structure of the sheet itself. As used here, this elevation difference is expressed as the "overall surface depth". The base sheets useful for this invention may possess three dimensionality and may have an overall surface depth of about 0.1 millimeter, or greater, more specifically about 0.3 millimeter or greater, even more specifically about 0.4 millimeter or greater, yet more specifically from about 0.5 millimeters or greater, and even more specifically from about 0.4 to about 0.8 millimeters. However, products made essentially of flat tissue are within the scope of certain embodiments of the present invention as well.
The three-dimensional structure of a very flat sheet can be described in terms of surface topography. Rather than presenting an almost flat surface, as is typical of a conventional paper, the three-dimensional sheets useful in producing the present invention can have significant topographic structures so that, in one embodiment, they can be driven in part from the use of the fabrics of continuous sculpting such as those mentioned by Chiu et al. in U.S. Patent No. 5,429,686, previously incorporated by reference. The resulting base sheet surface topography typically comprises a regular repeat unit cell that is typically a parallelogram with sides of about 2 and 20 millimeters in length. For wet laid materials, these three-dimensional base sheet structures can be created by wet sheet molding or they can be created before drying rather than by creping or engraving other operations after the sheet has dried. In this way, the three-dimensional base sheet structure is more feasible to be retained with wetting, helping to provide a high wet elasticity and to promote a good permeability in plane. For the base sheets placed by air, the structure can be imparted by the thermal etching of a fibrous mat with binder fibers that are activated by heat. For example, in a fibrous mat placed by air containing hot melt or thermoplastic binder fibers it can be heated and then etched before the structure is cooled to permanently give the sheet a three-dimensional structure.
In addition to the regular geometric structure imparted by the sculpted fabrics and other fabrics used to create a base sheet, an additional fine structure with a flat length scale of less than about 1 millimeter, may be present in the base sheet . Such fine structure can be derived from micro-beams created during the transfer of differential speed of the fabric from one fabric or wire to another before drying. Some of the materials of the present invention, for example, appear to have a fine structure with a fine surface depth of 0.1 millimeters or more, and sometimes 0.2 millimeters or more, when the height profiles are measured using a system of commercial moire interferometer. These fine peaks have a typical average width of less than 1 millimeter. The fine structure of the differential velocity transfer and other measurements can be useful to provide additional smoothness, flexibility and volume. The measurement of the surface structures is described below.
A particularly suitable method for measuring the overall surface depth is moire interferometry, which allows accurate measurements without surface deformation. For reference to the materials of the present invention, the surface topography should be measured using a computer controlled white light switched field moiré interferometer with around a 38 millimeter field of view. The principles of a useful implementation of such a system are described by Bieman et al. (L. Bieman, K.
Harding and A. Boehnlein, "Absolute Measurement Using Moiré de Changed Field ", procedures of the SPIE optical conference, volume 1614, pages 259-264, 1991. A suitable commercial instrument for moire interferometry is the interferometer CADEYES® produced by Medar. Inc., (from Farmington Hills, Michigan), built for a nominal 35 millimeter field of view, but with a real field of view of 38 millimeters (a field of vision within the range of 37 to 39.5 millimeters is adequate). The CADEYES® system uses white light which is projected through a grid to project fine black lines onto the surface of the sample. The surface is seen through a similar grid, creating moiré edges that are seen by a CCD camera. The appropriate lenses and the stepping motor adjust the optical configuration for the field change (a technique described below). A video processor sends the captured edge images to a PC computer for processing leaving the details of the surface height to be calculated back from the fringe patterns seen by the video camera.
In the moire CADEYES interferometry system, each pixel in the CCD video image is said to belong to a moiré band that is associated with a particular height range. The field change method, as described by Bieman et al. (L. Bieman, K. Harding and A. Boehnlein, "Absolute Measurement Using the Moiré de Campo Cambiado", procedures of the SPIE optical conference, volume 1614, pages 259 -264, 1991) and as originally patented by Boehnlein (U.S. Patent No. 5,069,548 incorporated herein by reference) is used to identify the strip number for each point in the video image (indicating to which strip it belongs a point) . The strip number is necessary to determine the absolute height at the measurement point in relation to a reference plane. A field change technique (sometimes called a phase change in art) is also used for sub-strip analysis (an accurate determination of the height of the measurement point within the high range occupied by its fringe). of field change coupled with a camera-based interferometry approach allows a fast and accurate absolute height measurement, allowing the measurement to be made despite possible height discontinuities on the surface. The technique allows an absolute height of each of the approximately 250,000 discrete points (pixels) on the sample surface that has been obtained, if appropriate optics, video equipment, data acquisition equipment and software that incorporates the Principles of moire interferometry with field change. Each measured point has a resolution of approximately 1.5 microns in its height measurement.
The computerized interferometry system is used to acquire topographic data and then generate a gray scale image of the topographic data, said image hereinafter called "the height map". The height map is displayed on a computer monitor, typically in 256 shades of gray and is based quantitatively on the topographic data obtained for the sample being measured. The resulting height map for the measurement area of 38 square millimeters can contain approximately 250,000 data points corresponding to approximately 500 pixels in both horizontal and vertical directions of the height map displayed. The pixel dimensions of the height map are based on a 512 x 512 CCD camera which provides images of moire patterns on the sample which can be analyzed by the computer software. Each pixel in the height map represents a height measurement at the corresponding x- and y- location on the sample. In the recommended system, each pixel has a width of approximately 70 micras, for example, represents a region on the sample surface of about 70 microns long in both directions in an orthogonal plane. This level of resolution prevents the singular fibers projecting above the surface from having a significant effect on the measurement of surface height. The height measurement in the z-direction must have a nominal accuracy of less than 2 microns and a range in the z-direction of at least 1.5 millimeters (for an additional background on the measurement method, see the product guide CADEYES, integral vision (formerly Medar, Inc.), of Farmington Hills, Michigan, 1994, or other CADEYES manuals and publications of Medar, Inc.).
The CADEYES system can measure up to 8 moiré fringes, with each fringe being divided into 256 depth counts (sub-fringe height increases, the smallest resolvable height difference). There will be 2,048 height accounts over the measurement range. This determines the range in the z-direction at which is approximately 3 millimeters in the 38-millimeter field of view instrument. If the variation of height in the field of vision covers more than 8 strips, a wrap around effect occurs, in which the ninth strip is labeled as if it were the first strip and the tenth stripe is labeled as the second, etc. In other words, the measured height will be changed by 2,048 depth counts. The exact measurement is limited to the main field of 8 stripes.
The moiré interferometer system, once installed and released from the factory to provide the range in the z-direction and the accuracy indicated above, can provide accurate topographic data for materials such as paper rolls. (Those skilled in the art can confirm the accuracy of factory calibration by performing measurements of surfaces with known dimensions). The tests are carried out in a room under TAPPI conditions (73 ° F, 50% relative humidity). The sample should be placed flat on the surface that is aligned or almost aligned with the measuring plane of the instrument and should be at such a height that both lower and higher regions of interest are within the measurement region of the instrument.
Once properly placed, data acquisition is initiated using the CADEYES® PC software and a height map of 150,000 data points is acquired and typically displayed within 30 seconds of the time data acquisition was initiated. (Using the CADEYES® system, the "contrast threshold level" for noise rejection is set to 1, providing some rejection of noise without excessive rejection of the data points). The reduction and display of data are achieved using CADEYES® software for PCs, which incorporates a customizable interconnection based on Microsoft Visual Basic Professional for Windows (version 3.0), running under Windows 3.1. The basic visual interconnection allows users to add custom analysis tools.
The height map of the topographic data can be used by those skilled in the art to identify characteristic unit cell structures (in the case of structures created by cloth patterns, these are typically parallelograms arranged as tiles to cover an area of two larger dimensions) and to measure the peak-to-valley depth of such structures. One sample method to do this is to extract two dimensional height profiles of lines drawn on the topographic height map which pass through the highest and lowest areas of the unit cells. These height profiles can be analyzed for the distance from peak to valley, if the profiles are then taken from a leaf or part of the leaf that was lying relatively flat when measured. To eliminate the effect of occasional optical noise and possible outcrops, the highest 10% and the lowest 10% of the profile should be excluded, and the height range of the remaining points is taken as the surface depth. Technically, the procedure requires calculating the variable width that we call "PÍO", defined to the difference of height between the lines of material of 10% and 90%, with the concept of lines of material being well known in the art, as explained by L. Mummery, in Surface Texture Analysis: The Manual, by Hommelwerke GMBH of Mühlhausen, Germany, 1990. An approach, which was illustrated with respect to figure 25, surface 831 is seen as a transition from air 832 to material 833. For a given profile 830, taken from a sheet that lies flat, the highest height at which the surface begins-the height of the highest peak-is the elevation of the "0% reference line" 834 or the "0% material line", meaning that 0% of the length of the horizontal line at that height is occupied by material. Along the horizontal line that passes through the lowest point of the profile, 100% of the line is occupied by material, making that line the "100% material line" 835. Between the material lines of 0 % and 100% (between the maximum and minimum points of the profile), the fraction of the horizontal line length occupied by the material will increase monotonically as the line elevation is decreased. The material proportion curve 836 gives the relationship between the material fraction along a horizontal line that passes through the profile and the height of the line. The material ratio curve is also the cumulative height distribution of a profile (a more accurate term can be "material fraction curve"). Once the material curve ratio is established, one can use it to define a characteristic peak height of the profile. The "typical peak to valley height" parameter is defined as the 837 difference between the heights of 10% of material line 838 and 90% of material line 839. This parameter is relatively robust in that outcrops or excursions Unusual from the typical profile structure have little influence on the PÍO height. The units of PÍO are millimeters. The overall surface depth of a material is reported as the PÍO surface depth value for the profile lines covering the height extremes of the typical unit cell of that surface. The "fine surface depth" is the PICO value for the profile taken along a surface region of the surface which is relatively uniform in height relative to the profiles that cover a maximum and a minimum of the unit cells . The measurements are reported for the more textured side of the base sheets of the present invention, which is typically the side that was in contact with the continuous drying fabric when the air flow is to the continuous dryer.
The overall surface depth is intended to examine the topography produced in the tissue tissue, especially those characteristics created on the sheet before and during the drying processes, but which is intended to exclude the large-scale topography "artificially" created from operations dry conversion such as weathered, perforated, gathered, etc. Therefore, the profiles examined should be taken from non-engraved regions if the tissue tissue has been recorded, or they should be measured on a non-etched tissue of tissue. The global surface depth measurements should exclude large-scale structures such as folds or bends which do not reflect the three-dimensional nature of the urinal base sheet itself. It is recognized that leaf topography can be reduced by calendering and other operations which affect the entire base sheet. The overall surface depth measurement can be carried out properly on a calendered base sheet.
The CADEYES® system with a 38-millimeter field of view can also be used to measure the height of material on an abrasive layer relative to the underlying tissue tissue, where there are openings in the adhesive layer that allow optical access to and measurement of the tissue tissue surface. When the abrasive layer comprises a translucent material, obtaining good optical measurements of the surface topography may require the application of white spray paint on the surface to increase the opacity of the surface being measured.
Test for the Abrasion index As used herein, the "abrasive index" is a measure of the ability of an abrasive layer to erode the material of a foam block that is moved on the surface of the abrasive layer in a prescribed manner under a fixed load. The abrasiveness index is reported as the mass lost in grams per foot of displacement of a block of heavy foam, multiplied by 100, when the foam is moved through a test cycle of sixteen inches. The method used is a modified form of ASTM F1015, "Standard Test Method for Relative Abrasivity of Synthetic Lawn Gaming Surfaces". A higher Abrasive Index is taken to be indicative of a more abrasive surface.
To prepare a measurement of the Abrasive Index, the foam test blocks are cut from a phenolic foam material to have dimensions of 1 inch by 1 inch by 1.25 inches. Foam is a well-known commercial green foam marketed as "dry floral foam", product code 665018 / 63486APP, manufactured by Oasis Floral Products, a division of Smithers-Oasis Company of Kent, Ohio (UPC 082322634866), commonly used for repairs Flowers for silk flowers and dried flowers.
A sample is cut from the material to be tested and taped to a flat rigid table surface using a two-sided Manco® exterior / interior carpet tape, marketed by Manco, Inc., of the Henkel Group of Avon, Ohio (UPC 075353071984). The tape is first placed on the surface of the table, preventing overlapping of the tape segments to ensure that an essentially uniform adhesive surface is provided having dimensions of at least 4 inches by 4 inches. The sample is then centered on the region with tape and pressed gently into place. A 3-inch by 3-inch square plastic block with a thickness of 1 inch and a mass of 168 grams is placed on the sample to define a test area that is centered within at least a region of 4 inches by 4 inches of the table that has the double-sided tape. A bronze cylinder, 2 inches in diameter with a mass of 1 kilogram is centered on the plastic block and allowed to reside for 10 seconds to secure the sample to the region with tape. A marker is used to trace around the edge of the plastic block to draw the test area. The block and the weight are removed from the sample. The sides of the drawn square (3 inches by 3 inches) should be aligned with the direction of the machine and the cross direction of the material when it is being tested when such instructions are defined (for example the warp direction for a woven abrasive layer).
Figure 24 is a layout scheme for the abrasivity index test for sample 280 to be tested. Sample 280 may have an upward facing abrasive layer 32 which may be attached to an underlying tissue tissue (not shown). The double-sided tape 270 joins the sample 280 to a sample surface (not shown). A foam block 274 is placed on the corner of the lower right side 282A of the square test region 272 marked on the upper surface of the sample 280. The dimensions of the surface of the foam block 274 which contacts the sample 280 are of 1 inch by 1 inch. On top of the foam block 274 is placed a brass weight of 100 grams 276 having a circular footprint of one inch in diameter. Two sides of the foam block 274 on the sample 280 are essentially over taxes on the inner boundary of the corner 282A of the marked test region 272.
To carry out the test (the foam block 274 is moved by hand from the corner of the lower right side 282A (the initial corner) to the upper right side corner 282B of the test region 272, and then the other corners 282C , and 282D, and back to 282A again, ensuring that the foam block 274 moves along but not outside the boundaries of the marked test area 272. Care must be taken not to apply a downward or upward force. by hand, but to apply only a stable lateral force to move the foam block 274 successively from one corner to another as indicated by arrows 278A-278D Both hands of the operator can be used as necessary to maintain the erect heavy foam block 274. The block is moved at a steady rate of about 5 seconds per side (one side being the path from one corner to the next corner.) The path traced by foam block 274 defines a square ending at the initial corner 282A.
To achieve a smooth and stable movement, one finger (for example the thumb) must be on the vertical "back" surface of the foam block 274 to push the block in the desired direction, and another strip must be on the vertical "front" surface "to maintain a stable position of the foam block 274.
After the block 274 has returned to the initial corner 282A, the path is inverted, again without lifting the heavy block 274. The block 274 therefore follows the same path as this one plotted but in the reverse order, going from the corner initial 282A to the lower left side corner 282D to the upper left side corner 282C to the upper right side corner 282B back to the initial lower right side corner 282A being moved by the stable lateral pressure and maintaining a rate of 5 seconds per side.
During this process, a portion of the foam block 274 will be removed by abrasion during the total 16-inch path that travels (two 8-inch cycles). The weight of 100 grams 276 is removed and the foam block 274 is then weighed and the amount of foam block 274 removed by the abrasion is determined by the recorded difference. This process is repeated twice more, using new materials (a new two-sided tape 270, new samples 280 of the same material being tested and new blocks of foam 274), allowing the lost mass to be determined three times. The average of the three measurements is taken and converted to mass loss by 12 inches by multiplication with the correction factor of 12/16 (for example, normalized to a 12-inch path), and then multiplied by 100. The parameter The resultant is reported as the abrasiveness index for the material being tested.
The abrasive layers of the present invention may have an abrasiveness index of about 1 or greater, about 2 or greater, about 3 or greater, about 4 or greater, or about 5 or greater, such as of from about 1.5 to 10, or from about 2 to about 7.
EXAMPLE 1 Preparation of a non-creped Continuous Dried Base Sheet To demonstrate an example of a texturized wet elastic absorbent fabric with improved dry feel, a suitable base sheet was prepared. The base sheet was produced on a continuous tissue manufacturing machine adapted for drying through non-creped air. The machine comprises a Fourdrinier forming section, a transaction, a continuous drying section, a subsequent transfer section and a reel. An aqueous solution diluted to approximately 1% consistency was prepared from 100% bleached chemo-thermomechanical pulp (BCTMP), pulped for 45 minutes at a consistency of about 4% before dilution. Bleached quimotermomechanical pulp is commercially available from Millar-Western 500/80/00 (Millar-Western, Meadow Lake, Saskatchewan, Canada). The wet strength agent Kymene 557LX manufactured by Hercules, Inc. (of Wilmington, Delaware) was added to the aqueous solution at a dose of about 16 kilograms of Kymene per ton of dry fiber, as was carboxymethylcellulose at a dose of 1.5 kilograms per ton of dry fiber. The solution was then deposited on a fine forming fabric and vented by the vacuum boxes to form a fabric with a consistency of about 12%. The fabric was then transferred to the transfer fabric (Lindsay Wire T-807-1) using a vacuum shoe to a first transfer point without any significant speed difference between the two fabrics, which were shifting to around 5.0 meters per second (980 feet per minute). The fabric was then transferred further from the transfer fabric to a continuous drying fabric to a second transfer point using a second vacuum shoe. The continuous drying fabric used was a Lindsay Wire T-116-3 design (from Lindsay Wire Division, Appleton Mills, Appleton, Wisconsin). The T-116-3 fabric is well suited to create molded three-dimensional structures. At the second transfer point, the continuous drying fabric was moving more slowly than the transfer fabric, with a differential speed of 27%. The fabric was then passed to a continuous dryer with cover where the leaf was dried. The dried sheet was then transferred from the continuous drying fabric to another fabric, from which the fabric was rolled. The basis weight of the dried base sheet was approximately 30 grams per square meter. The sheet had a thickness of about 1 millimeter, a total surface depth of about 0.4 millimeters, a geometric mean tensile strength of about 1,000 grams per 3 inches (measured with a jaw extension of 4 inches and a speed crosshead of 10 inches per minute at 50% relative humidity and 22.8 ° C), a ratio of wet tension: dry 45% in the transverse direction and a tension ratio in the machine direction: cross direction of 1.25 , and 17% stretch in the machine direction, 8.5% stretch in the transverse direction.
The permeability of the fabric was measured at 440 CFM.
EXAMPLE 2 A Laminate with a First Fabric of Polypropylene Blown with Fusion A high molecular weight isotactic polypropylene, Achieve 3915 manufactured by ExxonMobil Chemical Corporation (of Houston, Texas) was used in a pilot melt blowing facility to make a polymer network by meltblown fiberization. The molecular weight range of the polymer is around 130,000 to 140,000. According to the manufacturer, the melt flow rate of the polymer according to ASTM D1238 is 70 g / 10 minutes, which is believed to be below the range of melt flow rates for polymers typically used in an operation blowing with fusion; The polymer is normally used for a spinning operation or other applications other than meltblowing. (For example, a typical confusing blowing polymer such as the PP3546G polypropylene from ExxonMobil Chemical Corporation has a melt flow rate of 1,200 g / 10 minutes, measured according to ASTM D1238, and polypropylene PP3746G from the same manufacturer has a melt flow rate of 1,500 grams per 10 minutes). The high viscosity material was found to be surprisingly useful for producing the blown fabric with rough fusion according to the present invention.
The polypropylene was extruded through a melt blown die at 485 ° F onto a porous Teflon carrier fabric with an underlying vacuum. The tissue speed was 10 feet per minute. A melt blown polypropylene net with a base weight of 85 to 120 grams per square meter was generated by adjusting the temperature, air pressure and distance between the blow head to the training table, as well as the rate of polymer flow.
Figure 12 is a schematic drawing of a central cut-away part of the meltblown die 120 drawn according to the meltblown matrix used in this example. The primary part of the array comprises two side blocks 242 and 242 'and a triangular central supply block 244 through which the polymer is injected into an internal chamber 250. The central supply block 244 is essentially an isosceles triangle in section cross section, leading to a vertex 246 at an angle of 60 degrees. Along the apex 246 a series of evenly spaced holes 248 are drilled in fluid communication with the inner chamber 250. The inner chamber 250 is also in fluid communication with a pressurized source of melted polymer (not shown) which forces the melted polymer through the holes 248 of the central feed block 244 to form polymer yarns (not shown). The air jets 258 and 258 'flow through the cracks 252, 252', respectively, between the side blocks 242 and 242 'and the central supply block 244. The separations 252, 252' are in fluid communication with a pressurized air source (not shown) which generates the flow of the air jets 258 and 258 'towards the apex 246 of the central supply block 244. The air in the jets 258, 258' is typically heated well above the point melting of the polymer to prevent premature cooling of the polymer yarns. For this example, the air temperature was around 480 ° F. In a conventional meltblowing operation, the air jets 258 and 258 'provide a high level of cut that can cause an extensional thinning of the polymer yarns. and also provide a high level of turbulence to separate the threads and create fibers placed at random and isolated. For the purposes of the present invention, however, the air flow rate can be decreased to reduce turbulence by allowing some adjacent polymer strands of adjacent holes 248 to coalesce into multifilament aggregates, which still provide a flow of enough air and enough turbulence to deposit the polymer yarns as a network of fibers on an underlying carrier fabric (not shown).
The holes 248 have a diameter of 0.015 inches and were drilled at 30 per inch. The width of the active region of the matrix 120 (the region provided with the holes 248 for the formation of the polymer strands) was 11.5 inches. The entire matrix 120 was 14 inches wide. The separations 252 and 252 'have a width of 0.055 inches, determined by wedges placed between the central supply block 244 and the side blocks 242 and 242' at the outer ends of the matrix 120 (not shown) as outside the region. active The depth of drilling 256 of the holes 248 is the distance in the central supply block 244 that had to be penetrated during drilling for each central chamber 250. In this case, the drilling depth was around 4 millimeters. The height of the central supply block 244 (the distance from the base 254 to the apex 246) was 52 millimeters, and the depth of the inner chamber 250 (the height of the central supply block 244 minus the drilling depth 256) was of about 48 millimeters.
Not shown is a backing plate for the matrix block 120 through which the pressurized polymer melt was injected., air injection lines and support structures for the matrix. Such features are well known and readily provided by those skilled in the art. (It should be recognized that numerous alternatives to the meltblown matrix of Figure 12 are still within the scope of the present invention, such as a matrix with two or more rows of holes 248 that can be arranged in a stepped arrangement, parallel lines and the like, or matrices with annular jets or air surrounding the leaving polymer thread).
In the production of the blown fabric with fusion with rough multifilamentary aggregates, it was found that the "normal" rise of the meltblown matrix in relation to the carrier wire, namely 11 inches, was too high for the modified run conditions of according to the present invention. At this normal height, the yarns have cooled too much when they stick to the wire for a good fiber to fiber bond (here the term "fiber" encompasses multifilamentary aggregates), and the resulting fabric lacked integrity. The head was then lowered several inches, allowing a good fiber-fiber bond to occur. The distance from the matrix vertex to the carrier wire was about 7 inches. In practice, the optimum height for a given polymer will be a function of the speed of the fabric (and hence the flow rate of the polymer) and the temperatures of both the polymer and the heated air.
For the system shown in Figure 12, the conventional melt blow operation is achieved when the pressurized air source is applied to the air separations 252 and 252 'and is around 40 to 50 psig. For the present example, however, when lower air flow rates were desired to produce rougher fibers, the pressurized air source was set at about 12 psig at 20 psig during the runs to give a durable abrasive network with good material properties for the purposes of the present invention. Therefore, less than about half the air flow rate of the conventional melt blowing operation was used.
A micrometer (Fowler precision tools, model S2-550-020) was used to measure the diameter of the polypropylene fibers in the meltblown material. Twenty fibers were randomly selected and measured. A range of 70 micras to 485 micras was obtained, with an average of 250 microns and a standard deviation of 130 micras. The multifilamentary aggregates formed a significant part of the meltblown web.
The thickness variation test, as previously described, in a set of samples (the measured basis weight of 120 grams per square meter) gave a standard deviation of 0.25 millimeters (the average thickness was 1.18 millimeters) for the blown fabric with fusion. By way of comparison, a more conventional melt blown fabric was produced in Kimberly-Clark for commercial use with a basis weight of 39 grams per square meter and was measured to have a standard deviation of 0.03 millimeters (the average thickness was 0.29 millimeters). ).
The Gurley stiffness measurements of the melt blown fabric gave an average machine stiffness of 138.8 milligrams, with a standard deviation of 35.9 milligrams. The stiffness in the transverse direction was 150 milligrams, with a standard deviation of 34.0 milligrams. The base weight of the samples measured was 120 grams per square meter.
The air permeability of the blown tissue with fusion with multifilamentary aggregates was measured at 1130 CFM (medium of 6 samples). When two layers of melt blowing were over imposed, the air permeability for the two layers together was measured at 797 CFM (average of three measurement locations).
The meltblown fabric was bonded to the non-creped tissue of example 1. In a first run (run 2-A), the melt blown fabric was attached to a non-creped continuous tissue cutting section of the tissue to make a first laminate using a hot melt adhesive (NS-5610, National Starch Chemical Company of Berkeley , California) applied in a swirl pattern at 320 ° F with a hot melt applicator. The melt blown fabric showed excellent adhesion and worked well in scrubbing (high scratch resistance).
In a second run (run 2-B), the meltblown fabric was attached to the tissue to make a second laminate using the thermal bond achieved with a model plate 3953-006 of 1, 200 watts on the highest heat setting ("white linen"). The tissue of tissue cut to 3 inches by 6 inches was placed on a blown fabric with fusion cut to the same size and the plate was placed on the tissue and pressed with a gentle pressure (ca. two to three seconds, then rose and placed on an adjacent point. This was repeated several times, with each point of the tissue typically being connected to the plate two or three times, until the meltblown tissue bonded well with the tissue without the meltblown fabric losing its abrasive characteristics. (In practice, the temperature, application pressure and duration of heating was all optimized to make a particular product).
The air permeability of the sample cut from the laminate was measured at 316 CFM.
The surface topography of the second laminate was measured using moire interferometry as previously described. A field of view of 38 millimeters of optical head (nominally 35 millimeters) was used. To improve the opacity of the polypropylene fibers, the sample was lightly sprayed with a flat white spray paint using a Krylon® 1501 flat white paint can (from Sherwin-Williams, Cleveland Ohio), sprayed from a distance of about 6 inches with a sweeping motion and around 2 seconds of residence time for most parts of the painted laminate. The applied paint did not appear to fill or block the pores that were visible to the eye on the tissue, and did not appear to significantly modify the topography of the surface. The air permeability of the lightly painted laminate was measured at 306 CFM.
The multifilamentary aggregates had widths ranging from about 100 to about 500 microns. Several of the multifilamentary aggregates were turned 180 degrees or more over a short distance. Without wishing to be bound by one theory, it is believed that the common twist of the multifilamentary aggregates presents a more abrasive surface than if the multifilamentary aggregates remain essentially flat (relative to the tissue of paper) and not twisted. In an embodiment, a region of 3 square centimeters (3 centimeters by 3 centimeters) will have, over the average (based on sampling to at least 20 regions of 3 square centimeters representative) at least one multifilamentary aggregate doing a twist of at least 180 degrees around its axis. More specifically, there can be at least 5, at least 10, at least 15 or at least 50 multifilament aggregates that each suffer a twist along their respective axes of at least 180 degrees, and in one embodiment , at least 360 degrees or at least 720 degrees. In one embodiment, at least one multifilamentary aggregate in the 3-square-meter area had a helically twisted structure so that a 360-degree twist occurred within a distance of no more than 3 centimeters, more specifically not more than 1 centimeter , along the length of the fiber (following the path of the fiber).
For the lamination of run 2-B, the topography of the abrasive layer on the dried non-creped and underlying continuous tissue was measured using the CADEYES® system. The profile showed a variety of peaks and valleys corresponding to the elevated and depressed regions, respectively, along a profile line. The depth of surface along the profile line through the height map was 1,456 millimeters.
Ten samples were made from run 2-B and were tested for wet and dry opacity. The average dry opacity was 67.65% (standard deviation 1.14%), and the average wet opacity was 53.97% (standard deviation 3.1%), with an average of 1.60 grams of water per gram of fiber in the wet samples ( standard deviation 0.15 grams of water per gram of fiber). By way of comparison, a scouring cloth Chore Boy® Golden Fleecemarca (UPC # 0 26600 30316 7), marketed by Reckitt & Colman, Inc., of Wayne, New Jersey, showed a dry opacity of 95.1% for three samples, a wet opacity of 95.83%, and a water collection of 0.54 grams of water per gram of solid (standard deviation of 0.16). grams of water per gram of solid).
In a third run (run 2-C), the meltblown fabric was thermally bonded to a simple white SCOTT® towel (UPC 05400013431-core code JE2 11 290 01) produced by Kimberly-Clark Corporation (of Dallas, Texas) by ironing, as described in run 2-B indicated above. Air permeability was measured at 118 CFM, while the two samples of SCOTT® towel tissue alone taken from different rolls was measured at 147 CFM and 135 CFM. A sample of the melt blown fabric was simply placed on top of the SCOTT® towel fabric sample with an air permeability value of 135 CFM, placed on without thermal bonding of the two layers, giving an air permeability of 134 CFM, suggesting that the thermal bonding process causes clogging of some pores in the tissue tissue to slightly reduce the air permeability relative to an unbound combination of the tissue and the abrasive layer.
In a fourth run (run 2-D) the meltblown fabric was thermally bonded to a commercially available VIVA® towel, produced by Kimberly-Clark Corporation (of Dallas, Texas) by ironing, as described for run 2- B indicated above. The VIVA® towel was produced according to a double recrepado process using a latex adhesive. The air permeability was measured at 97.1 CFM.
In a related assay, a similar polypropylene was used to create another melt blown polymer fabric according to the methods described in this example.
Instead of Achieve 3915 polypropylene from ExxonMobil Chemical Corporation, Achieve 3825 polypropylene was used to produce a meltblown fabric with properties similar to those obtained with the Achieve 3915 polymer. Achieve 3825 polypropylene is a metallocene class polypropylene that has a melt flow rate of 32 grams per 10 minutes. The multifilamentary aggregates were also produced with characteristics similar to those obtained with the Achieve 3915 polymer. The higher back pressure was required to extrude the melted Achieve 3825 polymer, requiring about 400 psig compared to 280 psig for the Achieve 3915, due to the lowest melted flow rate.
EXAMPLE 3 A Second Blown Polypropylene Fabric with Fusion The Bassell PF015 polypropylene manufactured by Bassell North America (of Wilmington, Delaware) having a nominal processing temperature of about 221 ° C was used to produce a second meltblown polypropylene fabric to be used in the manufacture of the laminates with tissue . A different pilot installation of that of example 2 was used. The melt blown fabric was produced through a melt blow tip (30 holes per inch, hole diameter 0.0145 inches) producing 4 pounds per inch of machine width per hour (4 PIH). The roughness in the fiber was achieved by progressively lowering the processing temperatures and primary air pressure while targeting base weights ranging from about 50 grams per square meter to 100 grams per square meter. For meltblowing of 50 grams per square meter, line speed was 78 feet per minute, and for meltblowing 100 grams per square meter, the line speed was 39 feet per minute. The initial processing temperatures of about 260 ° C were lowered to between about 200 ° C to about 210 ° C, with the die tip at 210 ° C. The primary air pressure was lowered from the normal range of 3.5 -4 psig to less than 0.5 psig. The pressures of matrix point and rotation pump were around 170-190 psig and 340-370 psig, respectively. These placements were repeatedly reached in order to obtain a blown fabric with rough fusion, with good abrasiveness by virtue of being molded against the carrier wire. In a conventional operation, the meltblown fibers are relatively solidified when they land on the carrier wire and are not milled to a significant degree against the carrier wire, but in this case, the meltblown fibers were still sufficiently smooth so that these could conform to the texture of the carrier wire so that the meltblown fabric received a molded abrasive texture.
Meltblowing was formed at base weights of about 50 grams per square meter and about 100 grams per square meter as a product that was stopped only, and was also deted directly on the UCTAD fabric of example 1 and on the towels of VIVA® commercial paper. The melt blown fabric was only measured at a Gurley stiffness value in the average machine direction of 113.7 mg (standard deviation of 34.5 mg) and a Gurley stiffness value in the average transverse direction of 113.0 mg (standard deviation of 41.9 mg). The samples tested had a base weight of 100 gsm.
The thickness variation test in a set of high basis weight samples (base weight measured 100 gsm) gave a standard deviation of 0.07 mm (mean thickness was 0.99 mm) for the meltblown fabric.
The measurement of the air permeability for a single layer of the blown fabric with fusion of a value in excess of 1,500 CFM. Two tax layers of melt blown fabric gave an air permeability of 1168 CFM (average of the measurements in six places).
In a run (Run 3-A), the non-creped continuous drying fabric made in Example 1 was used, with 50 grams per square meter of melt blowing being formed directly on the tissue of tissue. The meltblowing layer gave a surface depth of about 0.728 millimeters. A repetitive structure was seen corresponding to the topography of the carrier wire against which the meltblown fabric was molded during forming. A unit cell of the repetitive structure, which was a parallelogram, had sides of about 9.5 millimeters and 1.5 millimeters. The laminate had a measured air permeability at 381 CFM (average of measurements at six locations).
Some process tests were also carried out by inverting the fabric after the meltblown layer had formed on a surface, and again by applying a meltblowing layer on the opte surface so that the tissue had an abrasive layer on both sides.
Another set of samples (run 3-D) were prepared by ironing the blown fabric with fusion with the tissue of example 1, following the ironing procedures given in example 2. Eight samples were tested for wet and dry opacity . The average dry opacity was 64.0% (standard deviation 0.82%), and the average wet opacity was 47.2% (standard deviation 2.2%), with an average of 1.59 grams of water per gram of fiber in the wet samples ( standard deviation 0.10 grams of water per gram of fiber).
Another laminate (run 3-C) was produced by forming the meltblown fabric directly on the VIVA® paper towel.
The laminates were also made by bonding the abrasive layer to a hydroentangled cleaner using a hot melt adhesive applied in a swirl pattern.
The cleaner, manufactured by Kimberly-Clark Corporation (of Dallas, Texas), was WypALL® and Teri® whose packages are commercialized with the United States of America Patent No. 5,284,703, granted on February 8, 1994 to Everhart and others. , which describes a comte fabric containing more than about 70%, by weight, of pulp fibers which are hydraulically entangled in a continuous filament substrate (eg, a spunbonded fabric).
EXAMPLE 4 Variation of the Second Fabric Blown with Fusion The melt blown fabric was made according to example 3, but with the various variations so that little molding could occur against the carrier wire (lower air temperature and larger distance from the die tip to the carrier wire, allowing the melt blown fibers to cool more quickly). Even though the fibers were even rougher than conventional meltblown fibers, the abrasiveness of the meltblown fabric was tangibly reduced due to the lack of large-scale topography imparted to the meltblown fabric. (The meltblown fabric appeared to be free of multifilament aggregates, which are believed to be present would have contributed to a superior abrasive characteristic regardless of the macroscopic topography imparted by the molding against a carrier wire).
EXAMPLE 5 Synergistic Material Properties To demonstrate the strength synergy and stretching synergy of several embodiments of the present invention, a stress test of the laminates and the unbonded layers was made using the first melt blown fabric of example 2. The results are shown in Table 1 given below, where the tests are reported as averages for multiple samples (five samples per measurement). The meltblown fabric had only an average tensile strength of 3393 grams per 3 inches (measured with a measuring length of 4 inches and 10-inches per minute crosshead speed with an Instron universal tester). When placed next to a sample of the Scott® towel (a tissue of dried tissue through commercial non-creped air comprising about 25% high performance pulp fibers and wet strength resins) but not bonded to these (the two fabrics were taxed and tested together), the tensile strength was 3707 g / 3 inches. When the meltblown fabric was thermally bonded (as described in Example 2) to the Scout® towel, the tensile strength increased to 5385 grams per 3 inches, an increase of 45%, giving a resistance synergy of 1.45. . The stretch synergy was 2.06.
In another run, the melt blown fabric was tested together with the non-creped and air dried tissue of example 1 (marked as "30 gsm UCTAD") giving an average tensile strength of 3565 g / 3 inches when the two fabrics were unbound, but with an average tensile strength of 3915 g / 3 inches for towels that were thermally bonded, for a strength synergy of about 1.10. The stretch synergy was 1.36.
In a third run, the VIVA® towel was used as the tissue. The resistance synergy was 1.22 and the stretch energy was 1.44.
Table 1. Resistance and Stretch Synergy Measurement EXAMPLE Abrasive Properties To illustrate the abrasivity of the products of the present invention and of the available commercial scrubbing materials, abrasive index tests were carried out for a variety of samples made according to the present invention, as described in examples 2 to 4, as well as for five commercial products put on the market for scrubbing and cleaning, the products each comprising an abrasive layer of material.
The five commercial products were: A) the 0-Cel-Omarca heavy-duty scouring pad (UPC 053200072056), marketed by 3M Home Care Products (of St. Paul, Minnesota), B) Scotch Britemarca heavy-duty scouring pad (UPC 051131502185), also marketed by 3M Home Care Products (St. Paul, Minn.), A product having a dark brown crosslinked polymeric material believed to comprise polypropylene and other materials, C) the delicate scouring sponge Scotch Britemarca (UPC 021200000027), also marketed by 3M Home Care Products (of St. Paul, Minnesota), the abrasive layer of this product was detached from the sponge for testing; D) Chore Boymarca scouring cloth Goleen Fleeceraarca (UPC 026600313167), marketed by Reckitt & Colman, Inc., (of Wayne, New Jersey), and E) a Sani-Tuffmarca cleaning cloth marketed by Kimberly-Clark Corporation (of Houston, Texas), which comprises a blown layer with green melting on a woven fabric. synthetic polymer (a heavier-melt blown fabric) with a basis weight of about 33 grams per square meter. The dry Sani-Tuffmarca cleaner had an air permeability of 98.5 CFM (average of three measurements).
Table 2 shows the results of the abrasive index. Interestingly, the meltblown fabric of Example 2 comprised a significant number of multifilament aggregates exhibiting the highest abrasive index (around 5.5). The 2-D run material, wherein the meltblown fabric of Example 2 had been pressed onto a relatively smooth VIVA® paper towel, showed a high abrasiveness index also (about 100%). 4. 25). The slightly lower abrasivity index compared to the isolated melt blown fabric itself was due to a slight decrease in the meltblown surface depth caused by the clamping process.
The meltblown fabric isolated from Example 3 exhibited a high abrasion index (about 4.5), although not as high as the meltblown fabric of Example 2, multifilament aggregates. This abrasive material had a macroscopic topography imparted by a rougher carrier fabric which is believed to have contributed to its abrasiveness. For Run 3-A, the meltblown fabric was no longer able to receive texture from the carrier wire, since it formed directly on the fabric of Example 1. However, the textured tissue is believed to provide a macroscopic topography to the meltblown fabric that provided good abrasivity, however, possibly due to the high abrasiveness index (around 4) for the material of the 3-A run. However, when the meltblown fabric in Example 2 was formed on a relatively smooth VIVA® paper towel, which lacks the distinctive topography and high surface depth of the UCTAD fabric, the resulting abrasivity index was relatively low. (about 1.25), thus pointing to the importance of meltblown tissue topography, where useful topographic features can be imparted by effective molding against a suitable carrier wire, or by the formation of blown tissue with fusion directly on a tissue of tissue having good topography (for example a surface depth of about 0.2 millimeters or greater, and optionally having a repeating pattern of peaks and valleys with a characteristic unit cell having an area of about 5 square millimeters or more, or about 8 square millimeters or plus) .
The meltblown fabric isolated from the example 4 was formed on the same carrier wire as in Example 3, but under conditions that did not effectively mold the blown fabric with fusion against the topography of the carrier wire, resulting in a relatively flat meltblown structure. It is believed that this accounts for the relatively low abrasiveness index (around 1) found for the meltblown fabric of Example 4. The meltblown fabric gave an air permeability of 973 CFM (average of 6 measurements on different locations). of the tissue).
The well-known abrasive characteristics of commercial products A, B and D are reflected in the relatively high abrasiveness index values. The commercial product E even when attempted for cleaning purposes employs a meltblown layer that lacks harshness or abrasive properties of many embodiments of the present invention, and exhibited a relatively low abrasivity index of about 0.75.
Table 2. Comparative Abrasive index values These and other modifications and variations of the present invention may be practiced by those of ordinary skill in the art without departing from the spirit and scope of the present invention which is more particularly set forth in the appended claims. In addition, it should be understood that the aspects of the various incorporations can be exchanged in whole or in part. In addition, those of ordinary skill in the art will appreciate that the foregoing description is by way of example only and that it is not intended to limit the invention thus described in such appended claims.

Claims (20)

RE I V I N D I C AC I ON E S
1. A scrubbing product that includes: a plurality of abrasive structures, the abrasive structures being configured in a stacked array; a clamping structure for releasably holding the plurality of abrasive structures together, the clamping structure allows an upper abrasive structure to be removed from the scrubbing product by a user to expose a subsequent abrasive structure.
2. A scouring product as claimed in clause 1, characterized in that the holding structure comprises a plurality of stitches so that the plurality of abrasive structures are held together by a thread.
3. A scrubbing product as claimed in clause 2, characterized in that the stitches are located around a periphery of the plurality of abrasive structures, each of the abrasive structures being perforated where the stitches are located to allow the release of the stitches. an abrasive structure of the remaining plurality.
4. A scouring product as claimed in clauses 2 or 3, characterized in that the stitches extend through either the scouring product or extend only through the plurality of abrasive structures.
5. A scouring product as claimed in clause 1, characterized in that the holding structure comprises a plurality of point-attached fastening points located between the adjacent layers of the abrasive structures.
6. A scouring product as claimed in clause 5, characterized in that the point-attached fastening points are either formed by an adhesive or comprise areas where the plurality of abrasive structures are melt-bonded together.
7. A scouring product as claimed in clause 1, characterized in that the holding structure keeps the plurality of abrasive structures together with a sufficient strength to allow the use of the scouring product without de-laminating the plurality of abrasive structures, the clamping structure, however, allows an upper abrasive structure to be removed from the product for scrubbing by a user, the clamping structure comprising the hook and loop fasteners located between the plurality of the abrasive structures.
8. A scouring product as claimed in clause 7, characterized in that the abrasive structures comprise an abrasive layer fastened to a fibrous cellulosic fabric, the abrasive layer comprises hooks, the cellulosic tissue defines a surface that can be fastened to the hooks of an adjacent abrasive structure.
9. A scouring product as claimed in clause 7, characterized in that the abrasive structures comprise a fibrous cellulose fabric fastened to an abrasive layer on one side and to a curl material on the opposite side.
10. A scrubbing product as claimed in any one of the preceding clauses, further characterized in that it comprises a liquid absorbent substrate having an upper surface and a bottom surface, the plurality of abrasive structures being attached to the upper surface.
11. A scrubbing product as claimed in clause 10, characterized in that the liquid absorbent substrate comprises a sponge, a foam, a non-woven material, or a tissue laminate.
12. A scouring product as claimed in clause 1, further characterized in that it comprises: a substrate; Y wherein the plurality of abrasive structures are wrapped around the substrate, each of the abrasive structures comprises an abrasive layer adhered to a fibrous cellulose fabric, wherein the abrasive structures are configured to be sequentially removed from the scouring product thereby exposing a structure unused abrasive that lies beneath the removed layer.
13. A scouring product as claimed in clause 12, characterized in that each abrasive structure forms an endless loop around the substrate or is spirally wound around the substrate.
14. A scouring product as claimed in clauses 12 or 13, characterized in that the abrasive structures are perforated.
15. A scrubbing product as claimed in any one of the preceding clauses, characterized in that each abrasive structure comprises an abrasive layer comprising abrasive polymer fibers in a non-uniform distribution secured to an absorbent layer comprising a fibrous cellulose fabric.
16. A scouring product as claimed in clause 15, characterized in that the cellulosic fabric comprises a continuously creped non-creped paper web.
17. A scrubbing product as claimed in clauses 15 or 16, characterized in that the absorbent layer comprises a fabric placed by air, a coform fabric, or a paper fabric.
18. A scouring product as claimed in clauses 15 to 17, characterized in that the abrasive polymeric fibers have a mean diameter greater than about 40 microns, and wherein the abrasive layer has a basis weight of more than about 50 grams. per square meter.
19. A scouring product as claimed in clauses 15 to 18, characterized in that the abrasive structures also contain an additive comprising a soap, a detergent, a buffering agent, an antimicrobial agent, an agent for the well-being of the skin, a lotion, a medication, a polishing agent or mixtures thereof.
20. A scouring product as claimed in any one of the preceding clauses, characterized in that the holding structure maintains the plurality of abrasive structures together with sufficient strength to allow the use of the scouring product without delamination of the abrasive structures. SUMMARY The present invention discloses a disposable scouring product for use in personal care or household cleaning applications. The scouring product of the invention is a multilayer laminating product and generally includes at least two distinct layers, a layer of abrasive and an absorbent fibrous layer such as a tissue of fiber to make paper, a layer of co-polymer. , a fabric placed by air, or combinations thereof. The abrasive layer is formed primarily of polymeric fibers in a random or random distribution as is typical of fibers deposited in meltblowing or spin-bonding processes to form a porous and open structure. In one embodiment, multiple layers of an abrasive structure are releasably fastened together. In this manner, the upper or outermost layer can be removed after having been used in order to expose an unused abrasive structure located under the discarded layer.
MXPA/A/2006/006057A 2003-12-11 2006-05-29 Disposable scrubbing product MXPA06006057A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10733169 2003-12-11

Publications (1)

Publication Number Publication Date
MXPA06006057A true MXPA06006057A (en) 2006-10-17

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