Fibrous sheet with improved properties

Information

  • Patent Grant
  • 11255051
  • Patent Number
    11,255,051
  • Date Filed
    Wednesday, November 29, 2017
    7 years ago
  • Date Issued
    Tuesday, February 22, 2022
    2 years ago
Abstract
A method for producing a foam-formed multilayered substrate that includes producing an aqueous-based foam including at least 3% by weight non-straight synthetic binder fibers, wherein the non-straight synthetic binder fibers have an average length greater than 2 mm; forming together a wet sheet layer from the aqueous-based foam and a cellulosic fiber layer, wherein the cellulosic fiber layer includes at least 60 percent by weight cellulosic fibers; and drying the combined layers to obtain the foam-formed multilayer substrate. A multilayered substrate includes a first layer including at least 60 percent by weight non-straight synthetic binder fibers having an average length greater than 2 mm; and a second layer including at least 60 percent by weight cellulosic fiber, wherein the first layer is in a facing relationship with the second layer, and wherein the multilayered substrate has a wet/dry tensile ratio of at least 60%.
Description
BACKGROUND

Many tissue products, such as facial tissue, bath tissue, paper towels, industrial wipers, and the like, are produced according to a wet laid process. Wet laid webs are made by depositing an aqueous suspension of pulp fibers onto a forming fabric and then removing water from the newly-formed web. Water is typically removed from the web by mechanically pressing water out of the web that is referred to as “wet-pressing.” Although wet-pressing is an effective dewatering process, during the process the tissue web is compressed causing a marked reduction in the caliper of the web and in the bulk of the web.


For most applications, however, it is desirable to provide the final product with as strength as possible without compromising other product attributes. Thus, those skilled in the art have devised various processes and techniques in order to increase the strength of wet laid webs. One process used is known as “rush transfer.” During a rush transfer process, a web is transferred from a first moving fabric to a second moving fabric in which the second fabric is moving at a slower speed than the first fabric. Rush transfer processes increase the bulk, caliper, and softness of the tissue web.


As an alternative to wet-pressing processes, through-drying processes have developed in which web compression is avoided as much as possible to preserve and enhance the web. These processes provide for supporting the web on a coarse mesh fabric while heated air is passed through the web to remove moisture and dry the web.


Additional improvements in the art, however, are still needed. In particular, a need currently exists for an improved process that includes unique fibers in a tissue web for increasing the bulk, softness, strength, and absorbency of the web without having to subject the web to a rush transfer process or to a creping process.


SUMMARY

In general, the present disclosure is directed to further improvements in the art of tissue and papermaking. Through the processes and methods of the present disclosure, the properties of a tissue web, such as bulk, strength, stretch, caliper, and/or absorbency can be improved. In particular, the present disclosure is directed to a process for forming a nonwoven web, particularly a tissue web containing pulp fibers, in a foam-forming process. For example, a foam suspension of fibers can be formed and spread onto a moving porous conveyor for producing an embryonic web.


In one aspect, for instance, the present disclosure is directed to a method for producing a foam-formed multilayered substrate that includes producing an aqueous-based foam including at least 3% by weight non-straight synthetic binder fibers, wherein the non-straight synthetic binder fibers have an average length greater than 2 mm; forming together a wet sheet layer from the aqueous-based foam and a cellulosic fiber layer, wherein the cellulosic fiber layer includes at least 60 percent by weight cellulosic fibers; and drying the combined layers to obtain the foam-formed multilayer substrate.


In another aspect, a multilayered substrate includes a first layer including at least 60 percent by weight non-straight synthetic binder fibers having an average length greater than 2 mm; and a second layer including at least 60 percent by weight cellulosic fiber, wherein the first layer is in a facing relationship with the second layer, and wherein the multilayered substrate has a wet/dry tensile ratio of at least 60%.


In yet another aspect, a multilayered substrate includes a first layer including at least 60 percent by weight non-straight synthetic binder fibers having an average length greater than 2 mm, wherein the non-straight synthetic binder fibers have a three-dimensional curly or crimped structure and are sheath-core bi-component fibers; and a second layer including at least 60 percent by weight cellulosic fiber, wherein the first layer is in a facing relationship with the second layer, wherein the multilayered substrate has a wet/dry tensile ratio of at least 60%, and wherein the multilayered substrate exhibits higher softness and absorbency than a homogeneous fibrous substrate with the same fiber composition.


Other features and aspects of the present disclosure are discussed in greater detail below.





BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other features and aspects of the present disclosure and the manner of attaining them will become more apparent, and the disclosure itself will be better understood by reference to the following description, appended claims and accompanying drawings, where:



FIG. 1 is a schematic illustration of a foam-formed wet sheet being transferred from a forming wire onto a drying wire on a simplified tissue line; and



FIG. 2 is a graphic illustration comparing the effect of layered versus non-layered substrates on wet/dry geometric mean tensile (GMT) ratio.





Repeat use of reference characters in the present specification and drawings is intended to represent the same or analogous features or elements of the present disclosure. The drawings are representational and are not necessarily drawn to scale. Certain proportions thereof might be exaggerated, while others might be minimized.


DETAILED DESCRIPTION

It is to be understood by one of ordinary skill in the art that the present discussion is a description of exemplary aspects of the present disclosure only, and is not intended as limiting the broader aspects of the present disclosure.


In general, the present disclosure is directed to the formation of tissue or paper webs having good bulk, strength, absorbency, and softness properties. Through the process of the present disclosure, tissue webs can be formed, for instance, having better stretch properties, improved absorbency characteristics, increased caliper, and/or increased softness. In one aspect, patterned webs can also be formed. In another aspect, for instance, a tissue web is made according to the present disclosure including the use of a foamed suspension of fibers.


High wet strength is important in towel products to have enough strength to hold together during hand drying or wiping up moisture. Standard towel sheets strive to have a wet/dry tensile of about 40% to have enough wet strength to work successfully. To achieve this level of wet strength in towels, refining and wet and dry strength chemistries are used.


The foam forming process opens up the opportunity to be able to add non-traditional fibers into the tissue making process. Fibers that normally would stay bundled together in the conventional wet laid process, such as longer length synthetic fibers, are now suspended and separated individually by foam bubbles, allowing the foam forming process to offer not only the capability to make novel materials with non-standard wet-laid fibers but also basesheets with enhanced properties. Further, foam forming allows the use of non-straight synthetic binder fibers.


As used herein, “non-straight” synthetic binder fibers include synthetic binder fibers (described below) that are curved, sinusoidal, wavy, short waved, U-shaped, V-shaped where the angle is greater than 15° but less than 180°, bent, folded, crimped, crinkled, twisted, puckered, flagged, double flagged, randomly flagged, defined flagged, undefined flagged, split, double split, multi-prong tipped, double multi-prong tipped, hooked, interlocking, cone shaped, symmetrical, asymmetrical, fingered, textured, spiraled, looped, leaf-like, petal-like, or thorn-like. Long non-straight fibers have advantages described herein, but can be difficult to employ in a typical wet-laid process that usually only employs wood pulp cellulosic fiber having a fiber length less than 5 mm and typically less than 3 mm. One example of a suitable non-straight synthetic binder fiber is T-255 synthetic binder fiber available from Trevira. T-255 synthetic binder fiber is a non-straight and crimped bi-component fiber with a polyethylene terephthalate (PET) core and a polyethylene (PE) sheath.


There are many advantages and benefits to a foam-forming process as described above. During a foam-forming process, water is replaced with foam (i.e., air bubbles) as the carrier for the fibers that form the web. The foam, which represents a large quantity of air, is blended with papermaking fibers. Because less water is used to form the web, less energy is required to dry the web. For instance, drying the web in a foam-forming process can reduce energy requirements by greater than about 10%, or such as greater than about 20%, in relation to conventional wet pressing processes.


Foam-forming technology has proven its capabilities in bringing many benefits to products including improved fiber uniformity, reduced water amount in the process, reduced drying energy due to both reduced water amount and surface tension, improved capability of handling an extremely long or short fiber that enables an introduction of long staple and/or binder fibers and very short fiber fine into a regular wet laying process, and enhanced bulk/reduced density that broadens one process to be able to produce various materials from a high to a very low density to cover multiple product applications.


Bench experimentation using a high speed mixer and surfactant has produced a very low density, between 0.008 to 0.02 g/cc, foam-formed fibrous materials. Based on these results, an air-formed, 3D-structured, nonwoven-like fibrous material can be produced using a low cost but high speed wet laying process. Previous attempts to produce such low density fibrous materials using typical foam-forming lines did not produce favorable results. Both processes have equipment limitations preventing production of a low density or high bulk foam-formed fibrous material. One process lacks a drying capability and therefore must use a press with high pressure to remove water from a formed wet sheet as much as possible to gain wet sheet integrity, so the sheet can be winded onto a roll. In addition, another process does not have a pressure roll but has a continuous drying tunnel. While the latter process appears to have a potential to produce a low density fibrous material, the foam-formed wet sheet must be transferred from a forming fabric to a drying metal wire before it is dried inside the drying tunnel. Again, to gain enough wet sheet integrity for this transfer, the foam-formed sheet must be dewatered as much as possible by vacuum prior to this transfer. As a result, most of entrapped air bubbles inside the wet sheet are also removed by the vacuum, resulting in a final dried sheet with a density similar to that of a sheet produced by a normal wet laying process.


Further experimentation resulted in the discovery that an addition of non-straight synthetic binder fibers reduces the final fibrous sheet density.


Without committing to a theory, it is believed that the non-straight synthetic binder fibers in a layered structure help to achieve a high wet/dry tensile ratio. Prior art uses of crimped (non-binder) fibers had the goal of achieving high bulk. The non-straight synthetic binder fiber of the present disclosure would not work well to achieve high bulk. Whereas the prior art required a crimped (non-binder) fiber having a fiber diameter at least 4 dtex, the non-straight synthetic binder fibers of the present disclosure do not have such a requirement. For example, one of the non-straight synthetic binder fibers used in the examples described below has a fiber diameter of 2.2 dtex.


According to the present disclosure, the foam-forming process is combined with a unique fiber addition for producing webs having a desired balance of properties.


In forming tissue or paper webs in accordance with the present disclosure, in one aspect, a foam is first formed by combining water with a foaming agent. The foaming agent, for instance, can include any suitable surfactant. In one aspect, for instance, the foaming agent can include an anionic surfactant such as sodium lauryl sulfate, which is also known as sodium laureth sulfate and sodium lauryl ether sulfate. Other anionic foaming agents include sodium dodecyl sulfate or ammonium lauryl sulfate. In other aspects, the foaming agent can include any suitable cationic, non-ionic, and/or amphoteric surfactant. For instance, other foaming agents include fatty acid amines, amides, amine oxides, fatty acid quaternary compounds, polyvinyl alcohol, polyethylene glycol alkyl ether, polyoxyethylene soritan alkyl esters, glucoside alkyl ethers, cocamidopropyl hydroxysultaine, cocamidopropyl betaine, phosphatidylethanolamine, and the like.


The foaming agent is combined with water generally in an amount greater than about 0.001% by weight, such as in an amount greater than about 0.005% by weight, such as in an amount greater than about 0.01% by weight, or such as in an amount greater than about 0.05% by weight. The foaming agent can also be combined with water generally in an amount less than about 0.2% by weight, such as in an amount less than about 0.5% by weight, such as in an amount less than about 1.0% by weight, or such as in an amount less than about 5% by weight. One or more foaming agents are generally present in an amount less than about 5% by weight, such as in an amount less than about 2% by weight, such as in an amount less than about 1% by weight, or such as in an amount less than about 0.5% by weight.


Once the foaming agent and water are combined, the mixture is combined with non-straight synthetic binder fibers. In general, any non-straight synthetic binder fibers capable of making a tissue or paper web or other similar type of nonwoven in accordance with the present disclosure can be used.


A binder fiber can be used in the foam formed fibrous structure of this disclosure. A binder fiber can be either a thermoplastic bicomponent fiber, such as PE/PET core/sheath fiber, or a water sensitive polymer fiber, such as polyvinyl alcohol fiber. Commercial binder fiber is usually a bicomponent thermoplastic fiber with two different melting polymers. Two polymers used in this bicomponent fiber usually have quite different melting points. For example, a PE/PET bicomponent fiber has a melting point of 120° C. for PE and a melting point of 260° C. for PET. When this bicomponent fiber is use as a binder fiber, a foam-formed fibrous structure including the PE/PET fiber can be stabilized by exposure to a heat treatment at a temperature slightly above 120° C. so that the PE fiber portion will melt and form inter-fiber bonds with other fibers while the PET fiber portion deliver its mechanical strength to maintain the fiber network intact. The bicomponent fiber can have different shapes with its two polymer components, such as, side-side, core-sheath, eccentric core-sheath, islands in a sea, etc. The core-sheath structure is the most commonly used in commercial binder fiber applications. Commercial binder fibers include T-255 binder fiber with a 6 or 12 mm fiber length and a 2.2 dtex fiber diameter from Trevira or WL Adhesion C binder fiber with a 4 mm fiber length and a 1.7 dtex fiber diameter from FiberVisions. The threshold amount of binder fiber to be added is generally dependent on the minimum that percolation theory would predict will provide a fiber network. For example, the percolation threshold is around 3% (by mass) for 6 mm, 2.2 dtex, T-255 fibers.


Once the foaming agent, water, and fibers are combined, the mixture is blended or otherwise subjected to forces capable of forming a foam. A foam generally refers to a porous matrix, which is an aggregate of hollow cells or bubbles that can be interconnected to form channels or capillaries.


The foam density can vary depending upon the particular application and various factors including the fiber furnish used. In one aspect, for instance, the foam density of the foam can be greater than about 200 g/L, such as greater than about 250 g/L, or such as greater than about 300 g/L. The foam density is generally less than about 600 g/L, such as less than about 500 g/L, such as less than about 400 g/L, or such as less than about 350 g/L. In one aspect, for instance, a lower density foam is used having a foam density of generally less than about 350 g/L, such as less than about 340 g/L, or such as less than about 330 g/L. The foam will generally have an air content of greater than about 40%, such as greater than about 50%, or such as greater than about 60%. The air content is generally less than about 80% by volume, such as less than about 75% by volume, or such as less than about 70% by volume.


To form the web, the foam is combined with a selected fiber furnish in conjunction with any auxiliary agents. The foam can be formed by any suitable method, including that described in co-pending U.S. Provisional Patent Application Ser. No. 62/437,974.


In general, any process capable of forming a paper web can also be utilized in the present disclosure. For example, a papermaking process of the present disclosure can utilize creping, double creping, embossing, air pressing, creped through-air drying, uncreped through-air drying, coform, hydroentangling, as well as other steps known in the art.


A standard process includes a foam-forming line that is designed to handle long staple fiber and is capable of achieving very uniform fiber mixing with other components. It is not, however, designed for producing high bulk fibrous material due to its equipment limitations as discussed above. FIG. 1 illustrates a simplified tissue line and demonstrates the difficulty in using this process to produce synthetic fibrous material, where a sheet is transferred between two wires. In this line, a frothed fibrous material or wet sheet 20 is formed onto a forming wire 30 by a headbox 35, where the wet sheet 20 has three layers of different compositions of fibrous materials when it is just laid onto the forming wire 30. The wet sheet 20 is then subjected to a vacuum to remove as much of water as possible so that when the wet sheet 20 travels to the end of the first forming wire 30, it gains enough integrity or strength to allow the wet sheet 20 to be transferred to a drying wire 40.


There is a contacting point 50 between the forming and drying wires 30, 40 where the wet sheet 20 is transferred from the forming wire 30 and to the drying wire 40. After the wet sheet 20 is transferred to the drying wire 40, the wet sheet 20 keeps contact with but can fall from the drying wire 40 if the wet sheet 20 does not have sufficient amount of adhesion to overcome gravity. After the transfer, the wet sheet 20 is positioned underneath the drying wire 40. The wet sheet 20 needs to be adhered to the drying wire 40 before it reaches a through-air dried (TAD) dryer or other suitable dryer (not shown). When a wet sheet 20 contains majority of cellulosic fiber, the wet sheet 20 has a water absorption capability to keep water sufficient enough so that the wet sheet 20 adheres to the drying wire 40 without being fallen off the drying wire 40 by gravity. When a wet sheet 20 contains too much synthetic fiber, such as greater than 30%, the wet sheet 20 starts to fall or separate off the drying wire 40 due to gravity. In this method, the wet sheet 20 when containing more than 30% synthetic fiber did not have sufficient adhesion to keep the sheet attached to the drying wire 40 shown in FIG. 1.


Therefore, current processes prevent the production of any frothed material with more than 30% synthetic fibers. As a result, a modified process or a new fibrous composition is needed to produce a foam formed sheet with a high wet/dry tensile ratio. The present disclosure addresses this shortfall by forming a layered wet sheet 20 with two outer layers including a majority of cellulosic fiber and a center layer including a majority of synthetic binder fiber. This improved method overcomes the weak wire adhesion issue and at the same time achieves several benefits. First, binder fiber can be concentrated to almost 100% in the center layer to form a fully-bonded fiber network to achieve a high strength while keep overall synthetic fiber portion below 50%, or even below 30%, such that the final tissue remains cellulosic fiber based. A non-layered structure cannot achieve this. Second, the layered structure creates a non-uniform bonding point distribution. Most of the bonds are formed within the center layer among the binder fibers themselves with only slight bonding among the cellulosic fibers located in two outer layers. This arrangement allows the tissue to exhibit a high strength, high wet/dry tensile ratio, high bulk, high absorbency, and significantly enhanced overall softness.


All tissue sheets described herein are manufactured in un-creped through-air dried (UCTAD) mode. The UCTAD process uses vacuum to transfer the wet sheet from one fabric to another, as illustrated in FIG. 1. Learnings from previous foam forming trials have shown that adding more than about 30% synthetic fiber in a homogeneous sheet affects the ability of the sheet to transfer. This is due to insufficient water in the sheet for the vacuum to work. In the present disclosure this shortcoming was solved by making a multilayered substrate with cellulosic fibers for one or more outer layers using conventional wet-laid process parameters (pulp slurry run from machine chests using standard pumps and settings), with the center layer foam formed (run from dump chests where the foam slurry of non-straight synthetic binder fiber was generated by adding surfactant and mixed). The refined cellulose outer layers, because refined fibers hold more water, hold enough water to allow the sheet to be transferred. For this disclosure, a layer with up to 80% non-straight synthetic binder fibers was foam formed for the center layer.


In various aspects of the present disclosure, a multilayered substrate can include one cellulosic fiber outer layer (by wetlaid or other process) and one foam formed synthetic binder fiber middle layer, or two cellulosic fiber outer layers (by wetlaid or other process) and one foam formed synthetic binder fiber middle layer. The one or two outer layers can also be foam formed and also contain low percentage amount of synthetic fiber if additional benefits can be obtained. Preferred aspects include at least one layer that is foam formed and includes a high percentage of synthetic binder fiber to give the multilayered substrate a high wet/dry tensile ratio. Preferred aspects also include at least one outer layer that maintains direct contact with the drying wire 40 after sheet transfer, where that at least one outer layer includes a high percentage of cellulosic fiber to have sufficient sheet-wire adhesion during processing. Other layers added to the multilayered substrate can have any combination of foam formed and wetlaid layers and can include any amount of cellulosic and/or synthetic fibers.


One or more layers of a multilayered substrate can include cellulosic fibers including those used in standard tissue making. Fibers suitable for making tissue webs include any natural and/or synthetic cellulosic fibers. Natural fibers can include, but are not limited to, nonwoody fibers such as cotton, abaca, kenaf, sabai grass, flax, esparto grass, straw, jute hemp, bagasse, milkweed floss fibers, bamboo fibers, and pineapple leaf fibers; and woody or pulp fibers such as those obtained from deciduous and coniferous trees, including softwood fibers, such as northern and southern softwood kraft fibers; and hardwood fibers, such as eucalyptus, maple, birch, and aspen. Pulp fibers can be prepared in high-yield or low-yield forms and can be pulped in any known method, including kraft, sulfite, high-yield pulping methods, and other known pulping methods. Fibers prepared from organosolv pulping methods can also be used.


A portion 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. Regenerated or modified cellulose fiber types include rayon in all its varieties and other fibers derived from viscose or chemically-modified cellulose. Chemically-treated natural cellulosic fibers can be used such as mercerized pulps, chemically stiffened or crosslinked fibers, or sulfonated fibers. For good mechanical properties in using papermaking fibers, it can be desirable that the fibers be relatively undamaged and largely unrefined or only lightly refined. While recycled fibers can be used, virgin fibers are generally useful for their mechanical properties and lack of contaminants. Mercerized fibers, regenerated cellulosic fibers, cellulose produced by microbes, rayon, and other cellulosic material or cellulosic derivatives can be used. Suitable papermaking fibers can also include recycled fibers, virgin fibers, or mixes thereof. In certain aspects capable of high bulk and good compressive properties, the fibers can have a Canadian Standard Freeness of at least 200, more specifically at least 300, more specifically still at least 400, and most specifically at least 500.


Other papermaking fibers that can be used in the present disclosure include paper broke or recycled fibers and high yield fibers. High yield pulp fibers are those papermaking fibers produced by pulping processes providing a yield of about 65% or greater, more specifically about 75% or greater, and still more specifically about 75% to about 95%. Yield is the resulting amount of processed fibers expressed as a percentage of the initial wood mass. Such pulping processes include bleached chemithermomechanical pulp (BCTMP), chemithermomechanical pulp (CTMP), pressure/pressure thermomechanical pulp (PIMP), thermomechanical pulp (TMP), thermomechanical chemical pulp (TMCP), high yield sulfite pulps, and high yield kraft pulps, all of which leave the resulting fibers with high levels of lignin. High yield fibers are well known for their stiffness in both dry and wet states relative to typical chemically pulped fibers.


Other optional chemical additives can also be added to the aqueous papermaking furnish or to the formed embryonic web to impart additional benefits to the product and process. The following materials are included as examples of additional chemicals that can be applied to the web. The chemicals are included as examples and are not intended to limit the scope of the disclosure. Such chemicals can be added at any point in the papermaking process.


Additional types of chemicals that can be added to the paper web include, but are not limited to, absorbency aids usually in the form of cationic, anionic, or non-ionic surfactants, humectants and plasticizers such as low molecular weight polyethylene glycols and polyhydroxy compounds such as glycerin and propylene glycol. Materials that supply skin health benefits such as mineral oil, aloe extract, vitamin E, silicone, lotions in general, and the like can also be incorporated into the finished products.


In general, the products of the present disclosure can be used in conjunction with any known materials and chemicals that are not antagonistic to its intended use. Examples of such materials include but are not limited to odor control agents, such as odor absorbents, activated carbon fibers and particles, baby powder, baking soda, chelating agents, zeolites, perfumes or other odor-masking agents, cyclodextrin compounds, oxidizers, and the like. Superabsorbent particles can also be employed. Additional options include cationic dyes, optical brighteners, humectants, emollients, and the like.


The basis weight of tissue webs made in accordance with the present disclosure can vary depending upon the final product. For example, the process can be used to produce bath tissues, facial tissues, paper towels, industrial wipers, and the like. In general, the basis weight of the tissue products can vary from about 6 gsm to about 120 gsm, or such as from about 10 gsm to about 90 gsm. For bath tissue and facial tissues, for instance, the basis weight can range from about 10 gsm to about 40 gsm. For paper towels, on the other hand, the basis weight can range from about 25 gsm to about 80 gsm.


The tissue web bulk can also vary from about 3 cc/g to about 30 cc/g, or such as from about 5 cc/g to 15 cc/g. The sheet “bulk” is calculated as the quotient of the caliper of a dry tissue sheet, expressed in microns, divided by the dry basis weight, expressed in grams per square meter. The resulting sheet bulk is expressed in cubic centimeters per gram. More specifically, the caliper is measured as the total thickness of a stack of ten representative sheets and dividing the total thickness of the stack by ten, where each sheet within the stack is placed with the same side up. Caliper is measured in accordance with TAPPI test method T411 om-89 “Thickness (caliper) of Paper, Paperboard, and Combined Board” with Note 3 for stacked sheets. The micrometer used for carrying out T411 om-89 is an Emveco 200-A Tissue Caliper Tester available from Emveco, Inc., Newberg, Oreg. The micrometer has a load of 2.00 kilo-Pascals (132 grams per square inch), a pressure foot area of 2500 square millimeters, a pressure foot diameter of 56.42 millimeters, a dwell time of 3 seconds and a lowering rate of 0.8 millimeters per second.


In multiple ply products, the basis weight of each tissue web present in the product can also vary. In general, the total basis weight of a multiple ply product will generally be the same as indicated above, such as from about 15 gsm to about 120 gsm. Thus, the basis weight of each ply can be from about 10 gsm to about 60 gsm, or such as from about 20 gsm to about 40 gsm.


EXAMPLES

For the present disclosure, basesheets were made using a standard three-layered headbox. This headbox structure allows both layered and homogeneous (all fibers types mixed together throughout the sheet) structures to be produced. Both sheet structures were made to support this disclosure.


Examples for the present disclosure include a layered sheet with 100% cellulose for the outer layers using conventional wet-laid process parameters (pulp slurry run from machine chests using standard pumps and settings). The center layer was foam formed, run from dump chests where the foam slurry of 100% T-255 synthetic binder fiber was generated by adding surfactant and mixed. A layer of up to 40% synthetic fiber was foam formed for the center layer.


The different tissue codes generated for this disclosure are described in Table 1, along with the properties each tissue code demonstrated.









TABLE 1







Tissue Compositions and Properties











Structure

Tissue Properties














Foam
Composition
Caliper
Density
Dry
Wet/dry















Code
Layered
formed
Outer layers
Middle layer
(mil)
(g/cc)
GMT
GMT Ratio


















1
Y
Middle layer
30% Euc
40% T-255 6 mm
TBD
TBD
1821
0.99


2
Y
Middle layer
40% Euc
20% T-255 6 mm
TBD
TBD
952
0.76


3
Y
Middle layer
45% Euc
10% T-255 6 mm
39.9
0.039
399
No reading














4
N
All layers
90% Euc, 10% T-255 6 mm
40.4
0.039
462
0.29


5
N
All layers
80% Euc, 20% T-255 6 mm
35.2
0.045
433
0.35









The basis weights were 40.5 gsm for Code 1, 42 gsm for Code 2, and 40 gsm for Codes 3-5. Euc is eucalyptus. Codes 2 and 5 show a direct comparison between layered and mixed substrates using the same overall fiber amounts.


GMT is geometric mean tensile strength that takes into account the machine direction (MD) tensile strength and the cross-machine direction (CD) tensile strength. For purposes herein, tensile strength can be measured using a SINTECH tensile tester using a 3-inch jaw width (sample width), a jaw span of 2 inches (gauge length), and a crosshead speed of 25.4 centimeters per minute after maintaining the sample under TAPPI conditions for 4 hours before testing. The “MD tensile strength” is the peak load per 3 inches of sample width when a sample is pulled to rupture in the machine direction. Similarly, the “CD tensile strength” represents the peak load per 3 inches of sample width when a sample is pulled to rupture in the cross-machine direction. The GMT is the square root of the product of the MD tensile strength and the CD tensile strength of the web. The “CD stretch” and the “MD stretch” are the amount of sample elongation in the cross-machine direction and the machine direction, respectively, at the point of rupture, expressed as a percent of the initial sample length.


More particularly, samples for tensile strength testing are prepared by cutting a 3 inch (76.2 mm) wide by at least 4 inches (101.6 mm) long strip in either the machine direction (MD) or cross-machine direction (CD) orientation using a JDC Precision Sample Cutter (Thwing-Albert Instrument Company, Philadelphia, Pa., Model No. JDC 3-10, Serial No. 37333). The instrument used for measuring tensile strength is an MTS Systems SINTECH Serial No. 1G/071896/116. The data acquisition software is MTS TestWorks® for Windows Ver. 4.0 (MTS Systems Corp., Eden Prairie, Minn.). The load cell is an MTS 25 Newton maximum load cell. The gauge length between jaws is 2±0.04 inches (76.2±1 mm). The jaws are operated using pneumatic action and are rubber coated. The minimum grip face width is 3 inches (76.2 mm), and the approximate height of a jaw is 0.5 inches (12.7 mm). The break sensitivity is set at 40 percent. The sample is placed in the jaws of the instrument, centered both vertically and horizontally. To adjust the initial slack, a pre-load of 1 gram (force) at the rate of 0.1 inch per minute is applied for each test run. The test is then started and ends when the force drops by 40 percent of peak. The peak load is recorded as either the “MD tensile strength” or the “CD tensile strength” of the specimen depending on the sample being tested. At least 3 representative specimens are tested for each product, taken “as is,” and the arithmetic average of all individual specimen tests is either the MD or CD tensile strength for the product.


Beside the significantly-enhanced wet/dry tensile ratio demonstrated in Table 1, data also indicated that the layered UCTAD tissues listed in Table 1 exhibit improved softness and absorbency, as shown in Table 2.


The two control codes described in Table 2 consist of a homogeneous mixed fiber sheet containing 100% cellulose pulp fiber (UCTAD Bath CHF controls from January 2015-September 2016). PBS stands for Premium Bath Score and is derived from the formulation below consisting of several Sensory Panel tests performed on the tissue basesheet.

PBS=5*(Average Fuzzy+Volume−Rigidity−Average Gritty)+25


The higher the PBS value, the softer the tissue is perceived to be. Table 2 demonstrates that layered structures, at the same strength, exhibit improved softness compared to homogeneous structures.









TABLE 2







Perceived Tissue Softness












Code
Basis Weight (gsm)
GMT (gf)
PBS
















1*
40.5
1272
64



2*
42
1054
64



Control Code A
40
1100
46



Control Code B
40
1300
41







Note:



*Codes 1 and 2 are the same materials as Codes 1 and 2 in Table 1, except that Codes 1 and 2 in Table 2 have been calendered.



GMT is geometric mean tensile strength and is described above in more detail.






Codes 1 and 2 were manufactured as bath tissue. As demonstrated in Table 3, the Codes 1 and 2 bath tissue with layered structures exhibited the same or slightly better absorbency than current commercial towel products. Towel products normally have higher absorbency than bath tissue. Absorption capacity is determined using a 4 inch by 4 inch specimen that is initially weighed. The weighed specimen is then soaked in a pan of test fluid (e.g. paraffin oil or water) for three minutes. The test fluid should be at least 2 inches (5.08 cm) deep in the pan. The specimen is removed from the test fluid and allowed to drain while hanging in a “diamond” shaped position (i.e., with one corner at the lowest point). The specimen is allowed to drain for three minutes for water and for five minutes for oil. After the allotted drain time the specimen is placed in a weighing dish and weighed. The absorbency of acids or bases having a viscosity more similar to water is tested in accordance with the procedure for testing the absorption capacity for water. Absorption Capacity (g)=wet weight (g)-dry weight (g); and Specific Absorption Capacity (g/g)=Absorption Capacity (g)/dry weight (g).









TABLE 3







Absorbency Data as Specific Absorption Capacity in g/g











Specific Absorption


Codes
Description
Capacity g/g












BOUNTY
Commercial
8.25


brand towels


BRAWNY
Commercial
9.06


brand towels


VIVA
Commercial
8.84


brand towels


Code 1*
CHF Layered eucalyptus 30%/
9.27



T-255 40%/eucalyptus 30%


Code 2*
CHF Layered eucalyptus 40%/
8.87



T-255 20%/eucalyptus 40%





Note:


*Codes 1 and 2 are the same materials as Codes 1 and 2 in Table 1, except that Codes 1 and 2 in Table 2 have been calendered.






It should be noted that while the examples in this disclosure were produced using a foam forming process, the disclosure should not be limited to such a process. The foam forming process is employed due to its capability of handling long fiber, such as 6 mm or 12 mm binder fiber. Conversely, if a short binder fiber (e.g., 2 mm or shorter) is used, the same layered structure can be produced using a standard water-forming process.


Results

As demonstrated in Tables 1-3, the layered structure with two cellulose fiber rich outer layers and one non-straight synthetic binder fiber rich middle layer exhibits a significant enhancement in wet/dry tensile ratio when compared to a substrate having the same fiber composition but homogenously mixed (i.e., a non-layered structure). This can be seen best in a comparison between Codes 2 and 5 in Table 1. Additional data is provided in FIG. 2, demonstrating the improvement in wet/dry tensile ratio in layered versus non-layered substrates having the same fiber compositions.


In a first particular aspect, a method for producing a foam-formed multilayered substrate includes producing an aqueous-based foam including at least 3% by weight non-straight synthetic binder fibers, wherein the non-straight synthetic binder fibers have an average length greater than 2 mm; forming together a wet sheet layer from the aqueous-based foam and a cellulosic fiber layer, wherein the cellulosic fiber layer includes at least 60 percent by weight cellulosic fibers; and drying the combined layers to obtain the foam-formed multilayer substrate.


A second particular aspect includes the first particular aspect, wherein the foam-formed layer has a dry density between 0.008 g/cc and 0.1 g/cc.


A third particular aspect includes the first and/or second aspect, wherein the non-straight synthetic binder fibers have an average length from 4 mm to 60 mm.


A fourth particular aspect includes one or more of aspects 1-3, wherein the non-straight synthetic binder fibers have an average length from 6 mm to 30 mm.


A fifth particular aspect includes one or more of aspects 1-4, wherein the non-straight synthetic binder fibers have a diameter of at least 1.5 dtex.


A sixth particular aspect includes one or more of aspects 1-5, wherein the non-straight synthetic binder fibers have a three-dimensional curly structure.


A seventh particular aspect includes one or more of aspects 1-6, wherein the non-straight synthetic binder fibers have a three-dimensional crimped structure.


An eighth particular aspect includes one or more of aspects 1-7, wherein the non-straight synthetic binder fibers are bi-component fibers.


A ninth particular aspect includes one or more of aspects 1-8, wherein the bi-component fibers are sheath-core bi-component fibers.


A tenth particular aspect includes one or more of aspects 1-9, wherein the sheath is polyethylene and the core is polyester.


An eleventh particular aspect includes one or more of aspects 1-10, wherein producing includes at least 10% by weight non-straight synthetic binder fibers.


A twelfth particular aspect includes one or more of aspects 1-11, wherein the multilayered substrate has a wet/dry tensile ratio of 60% or higher.


A thirteenth particular aspect includes one or more of aspects 1-12, wherein the cellulosic fibers are eucalyptus fibers.


In a fourteenth particular aspect, a multilayered substrate includes a first layer including at least 60 percent by weight non-straight synthetic binder fibers having an average length greater than 2 mm; and a second layer including at least 60 percent by weight cellulosic fiber, wherein the first layer is in a facing relationship with the second layer, and wherein the multilayered substrate has a wet/dry tensile ratio of at least 60%.


A fifteenth particular aspect includes the fourteenth particular aspect, wherein the multilayered substrate exhibits higher softness and absorbency than a homogeneous fibrous substrate with the same fiber composition.


A sixteenth particular aspect includes the fourteenth and/or fifteenth aspect, wherein the non-straight synthetic binder fibers have an average length from 6 mm to 30 mm and an average diameter of at least 1.5 dtex.


A seventeenth particular aspect includes one or more of aspects 14-16, wherein the non-straight synthetic binder fibers have a three-dimensional curly or crimped structure.


An eighteenth particular aspect includes one or more of aspects 14-17, wherein the non-straight synthetic binder fibers are sheath-core bi-component fibers.


A nineteenth particular aspect includes one or more of aspects 14-18, wherein the sheath is polyethylene and the core is polyester.


In a twentieth particular aspect, a multilayered substrate includes a first layer including at least 60 percent by weight non-straight synthetic binder fibers having an average length greater than 2 mm, wherein the non-straight synthetic binder fibers have a three-dimensional curly or crimped structure and are sheath-core bi-component fibers; and a second layer including at least 60 percent by weight cellulosic fiber, wherein the first layer is in a facing relationship with the second layer, wherein the multilayered substrate has a wet/dry tensile ratio of at least 60%, and wherein the multilayered substrate exhibits higher softness and absorbency than a homogeneous fibrous substrate with the same fiber composition.


These and other modifications and variations to the present disclosure can be practiced by those of ordinary skill in the art, without departing from the spirit and scope of the present disclosure, which is more particularly set forth in the appended claims. In addition, it should be understood that aspects of the various aspects of the present disclosure may be interchanged either in whole or in part. Furthermore, those of ordinary skill in the art will appreciate that the foregoing description is by way of example only, and is not intended to limit the disclosure so further described in such appended claims.

Claims
  • 1. A method for producing a foam-formed multilayered substrate, the method comprising: producing an aqueous-based foam including at least 3% by weight non-straight synthetic binder fibers, wherein the non-straight synthetic binder fibers have an average length greater than 2 mm;forming combined layers by combining together a wet sheet layer from the aqueous-based foam and a cellulosic fiber layer, wherein the cellulosic fiber layer includes at least 60 percent by weight cellulosic fibers;exposing the combined layers to heat such that at least a portion of the non-straight synthetic binder fibers melt to form inter-fiber bonds; anddrying the combined layers to obtain the foam-formed multilayer substrate.
  • 2. The method of claim 1, wherein the wet sheet layer from the aqueous-based foam has a dry density between 0.008 g/cc and 0.1 g/cc.
  • 3. The method of claim 1, wherein the non-straight synthetic binder fibers have an average length from 4 mm to 60 mm.
  • 4. The method of claim 1, wherein the non-straight synthetic binder fibers have an average length from 6 mm to 30 mm.
  • 5. The method of claim 1, wherein the non-straight synthetic binder fibers have a diameter of at least 1.5 dtex.
  • 6. The method of claim 1, wherein the non-straight synthetic binder fibers have a three-dimensional curly structure.
  • 7. The method of claim 1, wherein the non-straight synthetic binder fibers have a three-dimensional crimped structure.
  • 8. The method of claim 1, wherein the non-straight synthetic binder fibers are bi-component fibers.
  • 9. The method of claim 8, wherein the bi-component fibers are sheath-core bi-component fibers.
  • 10. The method of claim 9, wherein the sheath is polyethylene and the core is polyester.
  • 11. The method of claim 1, wherein producing includes at least 10% by weight non-straight synthetic binder fibers.
  • 12. The method of claim 11, wherein the multilayered substrate has a wet/dry tensile ratio of 60% or higher.
  • 13. The method of claim 12, wherein the foam-formed multilayered substrate is produced in an un-creped through-air dried mode.
  • 14. The method of claim 1, wherein the cellulosic fibers are eucalyptus fibers.
PCT Information
Filing Document Filing Date Country Kind
PCT/US2017/063653 11/29/2017 WO 00
Publishing Document Publishing Date Country Kind
WO2019/108172 6/6/2019 WO A
US Referenced Citations (700)
Number Name Date Kind
2105711 Weathered Jan 1938 A
2791523 Schoen May 1957 A
3007840 Wilcox Nov 1961 A
3506538 Friedberg et al. Apr 1970 A
3542640 Friedberg et al. Nov 1970 A
3615975 Gillern et al. Oct 1971 A
3716449 Gatward et al. Feb 1973 A
3798122 Appel Mar 1974 A
3837999 Chung Sep 1974 A
3839142 Clarke et al. Oct 1974 A
3871952 Robertson Mar 1975 A
3929560 Holik et al. Dec 1975 A
3938782 Robertson Feb 1976 A
3966540 Selander et al. Jun 1976 A
4007083 Ring et al. Feb 1977 A
4049491 Brandon et al. Sep 1977 A
4062721 Guyer et al. Dec 1977 A
4123787 Leclerc du Sablon et al. Oct 1978 A
4200488 Brandon et al. Apr 1980 A
4285767 Page Aug 1981 A
4288475 Meeker Sep 1981 A
4299655 Skaugen Nov 1981 A
4394930 Korpman Jul 1983 A
4415388 Korpman Nov 1983 A
4443232 Kaiser Apr 1984 A
4443297 Cheshire et al. Apr 1984 A
4443299 Cheshire et al. Apr 1984 A
4464224 Matolcsy Aug 1984 A
4478615 Kaiser Oct 1984 A
4483976 Yamamoto Nov 1984 A
4498956 Cheshire et al. Feb 1985 A
4543156 Cheshire et al. Sep 1985 A
4613627 Sherman et al. Sep 1986 A
4655950 Michalek Apr 1987 A
4686006 Cheshire et al. Aug 1987 A
4734321 Radvan et al. Mar 1988 A
4764253 Cheshire et al. Aug 1988 A
4773408 Cilento et al. Sep 1988 A
4773409 Cilento et al. Sep 1988 A
4778477 Lauchenauer Oct 1988 A
4883478 Lerailler et al. Nov 1989 A
4939030 Tsuji et al. Jul 1990 A
4944843 Wallace et al. Jul 1990 A
4948007 Berg et al. Aug 1990 A
4952448 Bullock et al. Aug 1990 A
4969975 Biggs et al. Nov 1990 A
4973382 Kinn et al. Nov 1990 A
4985467 Kelly et al. Jan 1991 A
5006373 Woodmansee et al. Apr 1991 A
5008306 Goguelin Apr 1991 A
5013405 Izard May 1991 A
5064653 Sessions et al. Nov 1991 A
5065752 Sessions et al. Nov 1991 A
5073416 Avakian et al. Dec 1991 A
5098778 Minnick Mar 1992 A
5102501 Eber et al. Apr 1992 A
5134959 Woodmansee et al. Aug 1992 A
5137551 Ahrens et al. Aug 1992 A
5147345 Young et al. Sep 1992 A
5153058 Hall et al. Oct 1992 A
5164045 Awofeso et al. Nov 1992 A
5178729 Janda Jan 1993 A
5196090 Corbellini et al. Mar 1993 A
5200035 Bhat et al. Apr 1993 A
5227023 Pounder et al. Jul 1993 A
5238534 Manning et al. Aug 1993 A
5260017 Giles Nov 1993 A
5260345 DesMarais et al. Nov 1993 A
5268224 DesMarais et al. Dec 1993 A
5300565 Berg et al. Apr 1994 A
5308565 Weber et al. May 1994 A
5318554 Young et al. Jun 1994 A
5328935 Van Phan et al. Jul 1994 A
5330822 Berg et al. Jul 1994 A
5331015 DesMarais et al. Jul 1994 A
5338766 Phan et al. Aug 1994 A
5344866 Hall Sep 1994 A
5348453 Baran et al. Sep 1994 A
5369007 Kidwell Nov 1994 A
5372766 Roe Dec 1994 A
5384179 Roe et al. Jan 1995 A
5387207 Dyer et al. Feb 1995 A
5393379 Parrinello Feb 1995 A
5397316 LaVon et al. Mar 1995 A
5397626 Berg et al. Mar 1995 A
5409572 Kershaw et al. Apr 1995 A
5428076 Roe Jun 1995 A
5434194 Fujimoto et al. Jul 1995 A
5451452 Phan et al. Sep 1995 A
5468437 Hall Nov 1995 A
5506046 Andersen et al. Apr 1996 A
5506277 Griesbach Apr 1996 A
5508072 Andersen et al. Apr 1996 A
5533244 Wadzinski Jul 1996 A
5536264 Hsueh et al. Jul 1996 A
5545450 Andersen et al. Aug 1996 A
5549589 Homey et al. Aug 1996 A
5550167 DesMarais Aug 1996 A
5560878 Dragoo et al. Oct 1996 A
5563179 Stone et al. Oct 1996 A
D375633 Spanagel et al. Nov 1996 S
5571849 DesMarais Nov 1996 A
5580624 Andersen et al. Dec 1996 A
5582670 Andersen et al. Dec 1996 A
5585432 Lee et al. Dec 1996 A
5586842 Bae et al. Dec 1996 A
5599334 Johnston et al. Feb 1997 A
5612385 Ceaser et al. Mar 1997 A
D378876 Spanagel et al. Apr 1997 S
5618341 Andersen et al. Apr 1997 A
5624971 Wilson Apr 1997 A
5626857 Thimineur et al. May 1997 A
5631053 Andersen et al. May 1997 A
5632737 Stone et al. May 1997 A
5633291 Dyer et al. May 1997 A
5649409 Gujer et al. Jul 1997 A
5650222 DesMarais et al. Jul 1997 A
D381810 Schultz et al. Aug 1997 S
5658603 Andersen et al. Aug 1997 A
5660900 Andersen et al. Aug 1997 A
5660903 Andersen et al. Aug 1997 A
5660904 Andersen et al. Aug 1997 A
5662731 Andersen et al. Sep 1997 A
5665442 Andersen et al. Sep 1997 A
5674917 Wilson Oct 1997 A
5679145 Andersen et al. Oct 1997 A
5679218 Vinson et al. Oct 1997 A
5683772 Andersen et al. Nov 1997 A
5691014 Andersen et al. Nov 1997 A
5692939 DesMarais Dec 1997 A
5693403 Brown et al. Dec 1997 A
5695607 Oriaran et al. Dec 1997 A
5702571 Kamps et al. Dec 1997 A
5705203 Andersen et al. Jan 1998 A
5705238 Andersen et al. Jan 1998 A
5705239 Andersen et al. Jan 1998 A
5705242 Andersen et al. Jan 1998 A
5707474 Andersen et al. Jan 1998 A
5707579 Habelski et al. Jan 1998 A
5709827 Andersen et al. Jan 1998 A
5709913 Andersen et al. Jan 1998 A
D390363 Baum et al. Feb 1998 S
5713881 Rezai et al. Feb 1998 A
5716563 Winterowd et al. Feb 1998 A
5716675 Andersen et al. Feb 1998 A
5719201 Wilson Feb 1998 A
5720851 Reiner Feb 1998 A
5728743 Dyer et al. Mar 1998 A
5736209 Andersen et al. Apr 1998 A
5741581 DesMarais et al. Apr 1998 A
5744506 Goldman et al. Apr 1998 A
5744509 Wilson et al. Apr 1998 A
5753308 Andersen et al. May 1998 A
5753359 Dyer et al. May 1998 A
5763499 DesMarais Jun 1998 A
5770634 Dyer et al. Jun 1998 A
5776388 Andersen et al. Jul 1998 A
5783126 Andersen et al. Jul 1998 A
5795921 Dyer et al. Aug 1998 A
5800416 Seger et al. Sep 1998 A
5800647 Andersen et al. Sep 1998 A
5810961 Andersen et al. Sep 1998 A
5817703 Blair et al. Oct 1998 A
5830305 Andersen et al. Nov 1998 A
5843055 Seger Dec 1998 A
5843544 Andersen et al. Dec 1998 A
5849155 Gasland Dec 1998 A
5849805 Dyer Dec 1998 A
5851634 Andersen et al. Dec 1998 A
5851648 Stone et al. Dec 1998 A
5853402 Faulks et al. Dec 1998 A
5863958 Dyer et al. Jan 1999 A
5868724 Dierckes et al. Feb 1999 A
5876643 Biggs et al. Mar 1999 A
5879722 Andersen et al. Mar 1999 A
5882479 Oriaran et al. Mar 1999 A
5899893 Dyer et al. May 1999 A
5900114 Brown et al. May 1999 A
5904809 Rokman et al. May 1999 A
5904812 Salman et al. May 1999 A
5908533 Marinack et al. Jun 1999 A
5916503 Rettenbacher Jun 1999 A
5916928 Sessions et al. Jun 1999 A
5919411 Rezai et al. Jul 1999 A
5922780 Dyer et al. Jul 1999 A
5925299 Dierckes et al. Jul 1999 A
5928741 Andersen et al. Jul 1999 A
5948829 Wallajapet et al. Sep 1999 A
5958186 Holm et al. Sep 1999 A
5976235 Andersen et al. Nov 1999 A
5985434 Qin et al. Nov 1999 A
6001218 Hsu et al. Dec 1999 A
6013293 De Moor Jan 2000 A
6013589 DesMarais et al. Jan 2000 A
6017833 Reiner et al. Jan 2000 A
6019871 Rokman et al. Feb 2000 A
6022615 Rettenbacher Feb 2000 A
6027610 Back et al. Feb 2000 A
6028018 Amundson et al. Feb 2000 A
6030673 Andersen et al. Feb 2000 A
6037282 Milding et al. Mar 2000 A
D423232 Reid Apr 2000 S
6051104 Oriaran et al. Apr 2000 A
6054022 Helwig et al. Apr 2000 A
6074527 Hsu et al. Jun 2000 A
6077390 Salman et al. Jun 2000 A
6077590 Archer et al. Jun 2000 A
6083211 DesMarais Jul 2000 A
6083586 Andersen et al. Jul 2000 A
6086718 Carter et al. Jul 2000 A
6090195 Andersen et al. Jul 2000 A
6093359 Gauchel et al. Jul 2000 A
6096809 Lorcks et al. Aug 2000 A
6103060 Munerelle et al. Aug 2000 A
6103063 Oriaran et al. Aug 2000 A
D430406 Ingalls Sep 2000 S
D430407 Ingalls Sep 2000 S
D430734 Bredendick et al. Sep 2000 S
6113740 Oriaran et al. Sep 2000 A
D431371 Ingalls et al. Oct 2000 S
D431372 Ingalls et al. Oct 2000 S
6133193 Kajikawa et al. Oct 2000 A
6136153 Rokman et al. Oct 2000 A
6136873 Hahnle et al. Oct 2000 A
6153053 Harper et al. Nov 2000 A
6160028 Dyer Dec 2000 A
6162961 Tanner et al. Dec 2000 A
6163943 Johansson et al. Dec 2000 A
D436738 Bredendick et al. Jan 2001 S
6168857 Andersen et al. Jan 2001 B1
6174152 Rokman et al. Jan 2001 B1
6174929 Hnle et al. Jan 2001 B1
D437119 Jahner et al. Feb 2001 S
D437120 Jahner et al. Feb 2001 S
D437489 Jahner et al. Feb 2001 S
D438017 Reid Feb 2001 S
6193838 Oriaran et al. Feb 2001 B1
6200404 Andersen et al. Mar 2001 B1
6203663 Kamps et al. Mar 2001 B1
6207244 Hesch Mar 2001 B1
D440051 Bredendick et al. Apr 2001 S
6214907 Tomka Apr 2001 B1
6231960 Dyer et al. May 2001 B1
6231970 Andersen et al. May 2001 B1
6235816 Lorcks et al. May 2001 B1
6238518 Rokman et al. May 2001 B1
D443766 Bredendick et al. Jun 2001 S
6243934 Wadzinski Jun 2001 B1
6245410 Hähnle et al. Jun 2001 B1
6245697 Conrad et al. Jun 2001 B1
6248211 Jennings et al. Jun 2001 B1
6251207 Schultz et al. Jun 2001 B1
6258203 Rokman et al. Jul 2001 B1
6261679 Chen et al. Jul 2001 B1
6274077 Hur et al. Aug 2001 B1
6280570 Harper et al. Aug 2001 B1
6287417 Bhat Sep 2001 B1
6287422 Harper et al. Sep 2001 B1
6296736 Hsu et al. Oct 2001 B1
6296929 Gentile et al. Oct 2001 B1
6309661 Haynes et al. Oct 2001 B1
6328850 Phan et al. Dec 2001 B1
6355142 Ahrens Mar 2002 B1
6372087 Harper et al. Apr 2002 B2
6376032 Clarke et al. Apr 2002 B1
6387210 Hsu et al. May 2002 B1
D459897 Bredendick et al. Jul 2002 S
6413368 Dwiggins et al. Jul 2002 B1
6419790 Leege et al. Jul 2002 B1
6425983 Marinack et al. Jul 2002 B1
6432272 Hollenberg et al. Aug 2002 B1
6436234 Chen et al. Aug 2002 B1
6440266 George et al. Aug 2002 B1
6443258 Putt et al. Sep 2002 B1
6444088 Rökman et al. Sep 2002 B2
6447640 Watson et al. Sep 2002 B1
6451166 Marinack et al. Sep 2002 B1
6455600 Hähnle et al. Sep 2002 B1
6472497 Loercks et al. Oct 2002 B2
6500302 Dwiggins et al. Dec 2002 B2
6503372 Rokman et al. Jan 2003 B1
6518479 Graef et al. Feb 2003 B1
6525240 Graef et al. Feb 2003 B1
6527913 Johnson et al. Mar 2003 B1
6531078 Laine et al. Mar 2003 B2
6540879 Marinack et al. Apr 2003 B2
6544386 Krzysik et al. Apr 2003 B1
6548132 Clarke et al. Apr 2003 B1
6562193 Elonen et al. May 2003 B1
6589634 Schultz et al. Jul 2003 B2
6596389 Hallett et al. Jul 2003 B1
6600086 Mace et al. Jul 2003 B1
6603054 Chen et al. Aug 2003 B2
6613424 Putt et al. Sep 2003 B1
6616802 Kinsley, Jr. et al. Sep 2003 B1
6630054 Graef et al. Oct 2003 B1
6649025 Mills et al. Nov 2003 B2
6657101 Malmgren et al. Dec 2003 B1
6663611 Blaney et al. Dec 2003 B2
6670522 Graef et al. Dec 2003 B1
6673980 Varona et al. Jan 2004 B1
6673983 Graef et al. Jan 2004 B1
6682215 Kinsley, Jr. et al. Jan 2004 B2
6689934 Dodge, II et al. Feb 2004 B2
6703330 Marsh Mar 2004 B1
6706944 Qin et al. Mar 2004 B2
6709548 Marinack et al. Mar 2004 B2
6709550 Holz et al. Mar 2004 B2
6733631 Elonen et al. May 2004 B2
6734335 Graef et al. May 2004 B1
6746570 Burazin et al. Jun 2004 B2
6749719 Burazin et al. Jun 2004 B2
6750262 Hähnle et al. Jun 2004 B1
6752907 Edwards et al. Jun 2004 B2
6780356 Putt et al. Aug 2004 B1
6787000 Burazin et al. Sep 2004 B2
6790314 Burazin et al. Sep 2004 B2
6797114 Hu Sep 2004 B2
6808790 Chen et al. Oct 2004 B2
6821385 Burazin et al. Nov 2004 B2
6821387 Hu Nov 2004 B2
6821388 Marsh Nov 2004 B2
6824650 Lindsay et al. Nov 2004 B2
6830656 Kinsley, Jr. Dec 2004 B2
6837956 Cowell et al. Jan 2005 B2
6837972 Marsh Jan 2005 B2
6861380 Garnier et al. Mar 2005 B2
6861477 Wang et al. Mar 2005 B2
6867346 Dopps et al. Mar 2005 B1
6875315 Bakken et al. Apr 2005 B2
6878238 Bakken et al. Apr 2005 B2
6887348 Hermans et al. May 2005 B2
6887350 Garnier et al. May 2005 B2
6893535 Hermans et al. May 2005 B2
6921459 Kinsley, Jr. et al. Jul 2005 B2
6924030 Kamada Aug 2005 B2
6939914 Qin et al. Sep 2005 B2
6946058 Hu Sep 2005 B2
6951598 Flugge et al. Oct 2005 B2
6956009 Wang et al. Oct 2005 B2
6962645 Graef et al. Nov 2005 B2
6964725 Shannon et al. Nov 2005 B2
6969781 Graef et al. Nov 2005 B2
6983821 Putt et al. Jan 2006 B2
D517816 Dwiggins et al. Mar 2006 S
7029756 Moline et al. Apr 2006 B2
D519739 Schuh et al. May 2006 S
7041196 Lorenz et al. May 2006 B2
7045026 Lorenz et al. May 2006 B2
7052580 Trokhan et al. May 2006 B2
7066006 Minerath, III et al. Jun 2006 B2
7067038 Trokhan et al. Jun 2006 B2
7081559 Fujikawa et al. Jul 2006 B2
7125470 Graef et al. Oct 2006 B2
7141142 Burazin et al. Nov 2006 B2
7155991 Minerath, III et al. Jan 2007 B2
7156954 Farrington, Jr et al. Jan 2007 B2
7160418 Edwards et al. Jan 2007 B2
7166190 Graef et al. Jan 2007 B2
7169451 Clarke et al. Jan 2007 B2
7214293 Trokhan et al. May 2007 B2
7220821 Hähnle et al. May 2007 B2
7229528 Vinson et al. Jun 2007 B2
7235708 Guidotti et al. Jun 2007 B2
D551406 Caruso et al. Sep 2007 S
7285183 Kajander et al. Oct 2007 B2
7287650 Koslow Oct 2007 B2
7291382 Krueger et al. Nov 2007 B2
7294238 Bakken et al. Nov 2007 B2
7300547 Luu et al. Nov 2007 B2
7311800 Russell et al. Dec 2007 B2
7314663 Stelljes, Jr. et al. Jan 2008 B2
7314664 Stelljes, Jr. et al. Jan 2008 B2
7314665 Stelljes, Jr. et al. Jan 2008 B2
7322970 Schmidt et al. Jan 2008 B2
7354502 Polat et al. Apr 2008 B2
7364015 Englert et al. Apr 2008 B2
7374638 Horenziak et al. May 2008 B2
7390378 Carels et al. Jun 2008 B2
7396436 Trokhan et al. Jul 2008 B2
7407560 Hilbig et al. Aug 2008 B2
7413629 Fisher et al. Aug 2008 B2
7416636 Blomqvist Aug 2008 B2
7416637 Murray et al. Aug 2008 B2
7435266 Sun et al. Oct 2008 B2
7435313 Boatman et al. Oct 2008 B2
7435316 Boatman et al. Oct 2008 B2
7494563 Edwards et al. Feb 2009 B2
7497923 Ward et al. Mar 2009 B2
7497925 Hermans et al. Mar 2009 B2
7497926 Hermans et al. Mar 2009 B2
7503998 Murray et al. Mar 2009 B2
7524399 Hermans et al. Apr 2009 B2
7524404 Boatman et al. Apr 2009 B2
7585388 Yeh et al. Sep 2009 B2
7585389 Yeh et al. Sep 2009 B2
7597777 Wilke, II Oct 2009 B2
7601374 Clarke Oct 2009 B2
7629043 Lindsay et al. Dec 2009 B2
7645359 Lorenz et al. Jan 2010 B2
7662257 Edwards et al. Feb 2010 B2
7670457 Murray et al. Mar 2010 B2
7678229 Wilke, II Mar 2010 B2
7678231 Dyer et al. Mar 2010 B2
7682697 Raghavendran et al. Mar 2010 B2
7691228 Edwards et al. Apr 2010 B2
7699959 Ward et al. Apr 2010 B2
7744576 Busam et al. Jun 2010 B2
7750203 Becker et al. Jul 2010 B2
7775958 Mukai et al. Aug 2010 B2
7785696 Boatman et al. Aug 2010 B2
7794565 Shannon et al. Sep 2010 B2
7799161 Schuh et al. Sep 2010 B2
7799968 Chen et al. Sep 2010 B2
7820008 Edwards et al. Oct 2010 B2
7828932 Hermans et al. Nov 2010 B2
7846296 Luu et al. Dec 2010 B2
7850823 Chou et al. Dec 2010 B2
7851057 Englert et al. Dec 2010 B2
7851667 Becker et al. Dec 2010 B2
7857941 Ruthven et al. Dec 2010 B2
7862686 Ward et al. Jan 2011 B2
7887676 Boatman et al. Feb 2011 B2
7918951 Lorenz et al. Apr 2011 B2
7918964 Edwards et al. Apr 2011 B2
7918972 Boatman et al. Apr 2011 B2
7927456 Murray et al. Apr 2011 B2
7972476 Scherb et al. Jul 2011 B2
7994079 Chen et al. Aug 2011 B2
8007640 Boatman et al. Aug 2011 B2
8017827 Hundorf et al. Sep 2011 B2
8056733 Koslow Nov 2011 B2
8083893 Boatman et al. Dec 2011 B2
8092848 Clarke Jan 2012 B2
8102275 McGuire et al. Jan 2012 B2
8110232 Clarke Feb 2012 B2
8123905 Luu et al. Feb 2012 B2
8142612 Murray et al. Mar 2012 B2
8142617 Ruthven et al. Mar 2012 B2
8143472 Bragd et al. Mar 2012 B1
8152957 Edwards et al. Apr 2012 B2
8152958 Super et al. Apr 2012 B2
8158689 Baker et al. Apr 2012 B2
8178025 Awofeso et al. May 2012 B2
8187240 Busam et al. May 2012 B2
8187427 Schuh et al. May 2012 B2
8211078 Noel Jul 2012 B2
8226797 Murray et al. Jul 2012 B2
8257552 Edwards et al. Sep 2012 B2
8293072 Super et al. Oct 2012 B2
8319005 Becker et al. Nov 2012 B2
8324446 Wang et al. Dec 2012 B2
8328985 Edwards et al. Dec 2012 B2
8361278 Fike et al. Jan 2013 B2
8378000 Hintz et al. Feb 2013 B2
8388803 Super et al. Mar 2013 B2
8388804 Super et al. Mar 2013 B2
8394236 Edwards et al. Mar 2013 B2
8398818 Edwards et al. Mar 2013 B2
8398820 Edwards et al. Mar 2013 B2
8425721 Tynkkynen et al. Apr 2013 B2
8435381 Murray et al. May 2013 B2
8461412 Febo et al. Jun 2013 B2
8496637 Hundorf et al. Jul 2013 B2
8512516 Murray et al. Aug 2013 B2
8524040 Edwards et al. Sep 2013 B2
8540846 Miller et al. Sep 2013 B2
8545676 Super et al. Oct 2013 B2
8552252 Hundorf et al. Oct 2013 B2
8562786 Murray et al. Oct 2013 B2
8568559 Murray et al. Oct 2013 B2
8568560 Murray et al. Oct 2013 B2
8603296 Edwards et al. Dec 2013 B2
8632658 Miller et al. Jan 2014 B2
8636874 Super et al. Jan 2014 B2
8647105 Awofeso et al. Feb 2014 B2
8652300 Super et al. Feb 2014 B2
8662344 Gispert Mar 2014 B2
8673115 Edwards et al. Mar 2014 B2
8674170 Busam et al. Mar 2014 B2
8702668 Noel Apr 2014 B2
8741105 Beaupre et al. Jun 2014 B2
8766031 Becker et al. Jul 2014 B2
8778138 Super et al. Jul 2014 B2
8791318 Becker et al. Jul 2014 B2
8815056 Araki et al. Aug 2014 B2
8829263 Haggstrom et al. Sep 2014 B2
8841506 Febo et al. Sep 2014 B2
8852397 Super et al. Oct 2014 B2
8864944 Miller et al. Oct 2014 B2
8864945 Miller et al. Oct 2014 B2
8911592 Edwards et al. Dec 2014 B2
8968516 Super et al. Mar 2015 B2
8979815 Roe et al. Mar 2015 B2
8980052 Super et al. Mar 2015 B2
9017517 Super et al. Apr 2015 B2
9044359 Wciorka et al. Jun 2015 B2
9051691 Miller et al. Jun 2015 B2
9057158 Miller et al. Jun 2015 B2
9138360 Febo et al. Sep 2015 B1
9144524 Febo et al. Sep 2015 B2
9216116 Roe et al. Dec 2015 B2
9216118 Roe et al. Dec 2015 B2
9228048 Wibaux et al. Jan 2016 B2
9241845 Hundorf et al. Jan 2016 B2
9243367 Rekoske et al. Jan 2016 B2
9267240 Lee et al. Feb 2016 B2
9279219 Edwards et al. Mar 2016 B2
9309627 Miller et al. Apr 2016 B2
9326896 Schafer et al. May 2016 B2
9333120 Lavon et al. May 2016 B2
9334610 Kinnunen et al. May 2016 B2
9340363 Jackels et al. May 2016 B2
9365977 Beaupre et al. Jun 2016 B2
9371614 Schuh et al. Jun 2016 B2
9371615 Super et al. Jun 2016 B2
9375358 Ehmsperger et al. Jun 2016 B2
9382665 Miller et al. Jul 2016 B2
9388534 Super et al. Jul 2016 B2
9447543 Matula Sep 2016 B2
9468566 Rosati et al. Oct 2016 B2
9476162 Lee et al. Oct 2016 B2
9492328 Jackels et al. Nov 2016 B2
9493911 Miller et al. Nov 2016 B2
9532910 Rosati et al. Jan 2017 B2
9572728 Ashton et al. Feb 2017 B2
9579238 Noel Feb 2017 B2
9603755 Tanaka Mar 2017 B2
9649232 Hippe et al. May 2017 B2
9649830 Rasch May 2017 B2
9657443 Rekoske et al. May 2017 B2
9662246 Collinson et al. May 2017 B2
9668926 Jackels et al. Jun 2017 B2
9708774 Lee et al. Jul 2017 B2
9713556 Arizti et al. Jul 2017 B2
9713557 Arizti et al. Jul 2017 B2
9739015 Miller et al. Aug 2017 B2
9744755 Thompson, Jr. et al. Aug 2017 B2
9752280 Matula Sep 2017 B2
9763835 Becker et al. Sep 2017 B2
9789009 Joseph Oct 2017 B2
9789011 Roe et al. Oct 2017 B2
9808554 Swaniker Nov 2017 B2
9822487 Ahoniemi et al. Nov 2017 B2
9877872 Mumby et al. Jan 2018 B2
9879382 Miller et al. Jan 2018 B2
9950309 Lee et al. Apr 2018 B2
9963568 Nakatsuji et al. May 2018 B2
9974697 Lavon et al. May 2018 B2
9974699 Kreuzer et al. May 2018 B2
9987176 Roe et al. Jun 2018 B2
9988763 Ramaratnam et al. Jun 2018 B2
9994712 Cai et al. Jun 2018 B2
9995005 Ramaratnam et al. Jun 2018 B2
10004647 Jackels et al. Jun 2018 B2
10022280 Ehrnsperger et al. Jul 2018 B2
10034800 Febo et al. Jul 2018 B2
10039673 Mumby et al. Aug 2018 B2
10039676 LaVon Aug 2018 B2
10052242 Bianchi et al. Aug 2018 B2
10065175 Lee et al. Sep 2018 B2
10071002 Bianchi et al. Sep 2018 B2
10076449 Allen et al. Sep 2018 B2
10099425 Miller, IV et al. Oct 2018 B2
10130519 Mumby et al. Nov 2018 B2
10130525 Rosati et al. Nov 2018 B2
10130527 Peri et al. Nov 2018 B2
10137039 Stelzig et al. Nov 2018 B2
10138600 Jannari et al. Nov 2018 B2
10149788 Kreuzer et al. Dec 2018 B2
10190263 Ramaratnam et al. Jan 2019 B2
10196780 Lee et al. Feb 2019 B2
10201644 Haggstrom et al. Feb 2019 B2
10208426 Sealey et al. Feb 2019 B2
10221350 Shalagina et al. Mar 2019 B2
10231874 Mumby et al. Mar 2019 B2
10245188 Jackels et al. Apr 2019 B2
10247195 Manninen et al. Apr 2019 B2
10253434 Nakamura Apr 2019 B2
10259151 Kiiskinen et al. Apr 2019 B2
10273635 Miller, IV et al. Apr 2019 B2
10292875 Tapp et al. May 2019 B2
10301775 Nordström et al. May 2019 B2
10301779 Sealey, II et al. May 2019 B2
10322040 Stiehl et al. Jun 2019 B2
10335324 Roe et al. Jul 2019 B2
10619303 Thole et al. Apr 2020 B2
11015292 Venema et al. May 2021 B2
11136700 Venema et al. Oct 2021 B2
20010013389 Fingal et al. Aug 2001 A1
20020007169 Graef et al. Jan 2002 A1
20020013560 Erspamer et al. Jan 2002 A1
20020055310 Falk et al. May 2002 A1
20020088581 Graef et al. Jul 2002 A1
20020092634 Rokman et al. Jul 2002 A1
20020132121 Palacio et al. Sep 2002 A1
20030106656 Johnson et al. Jun 2003 A1
20030134094 Zafiroglu et al. Jul 2003 A1
20030139715 Dodge et al. Jul 2003 A1
20030167045 Graef et al. Sep 2003 A1
20030171727 Graef et al. Sep 2003 A1
20030220039 Chen et al. Nov 2003 A1
20040045685 Horner et al. Mar 2004 A1
20040063367 Dodge et al. Apr 2004 A1
20040065420 Graef et al. Apr 2004 A1
20040084162 Shannon et al. May 2004 A1
20040084164 Shannon et al. May 2004 A1
20040096642 Maruyama et al. May 2004 A1
20040110017 Lonsky et al. Jun 2004 A1
20040111817 Chen et al. Jun 2004 A1
20040112783 Mukai et al. Jun 2004 A1
20040115419 Qin et al. Jun 2004 A1
20040115451 Lonsky et al. Jun 2004 A1
20040118530 Kressner et al. Jun 2004 A1
20040121680 Yahiaoui et al. Jun 2004 A1
20040127873 Varona et al. Jul 2004 A1
20040142620 Kinsley Jul 2004 A1
20040157524 Polat et al. Aug 2004 A1
20040254551 Carnes et al. Dec 2004 A1
20040256066 Lindsay et al. Dec 2004 A1
20050034826 Hu Feb 2005 A1
20050039870 Blomqvist Feb 2005 A1
20050060933 Henson Mar 2005 A1
20050090789 Graef et al. Apr 2005 A1
20050095980 Chang May 2005 A1
20050106223 Kelly May 2005 A1
20050124709 Krueger et al. Jun 2005 A1
20050136772 Chen et al. Jun 2005 A1
20050142348 Kajander et al. Jun 2005 A1
20050152954 Farrell et al. Jul 2005 A1
20050230069 Hilbig et al. Oct 2005 A1
20050244627 Travelute et al. Nov 2005 A1
20050247397 Kraus et al. Nov 2005 A1
20050247416 Forry et al. Nov 2005 A1
20050267226 Wehr et al. Dec 2005 A1
20060005916 Stelljes et al. Jan 2006 A1
20060011315 Kinsley et al. Jan 2006 A1
20060030632 Krueger et al. Feb 2006 A1
20060081348 Graef et al. Apr 2006 A1
20060135026 Arendt et al. Jun 2006 A1
20060141880 Bascom et al. Jun 2006 A1
20060142719 Vogt et al. Jun 2006 A1
20060191357 Minerath et al. Aug 2006 A1
20060266485 Knox et al. Nov 2006 A1
20060266487 Scherb et al. Nov 2006 A1
20070148433 Mallory et al. Jun 2007 A1
20070179210 Swaniker Aug 2007 A1
20070218485 Davis et al. Sep 2007 A1
20070269644 Harper et al. Nov 2007 A1
20080052859 Orlandi Mar 2008 A1
20080179775 Palm et al. Jul 2008 A1
20080312617 Hundorf et al. Dec 2008 A1
20080312618 Hundorf et al. Dec 2008 A1
20080312619 Ashton et al. Dec 2008 A1
20080312620 Ashton et al. Dec 2008 A1
20080312621 Hundorf et al. Dec 2008 A1
20080312622 Hundorf et al. Dec 2008 A1
20080312625 Hundorf et al. Dec 2008 A1
20080312628 Hundorf et al. Dec 2008 A1
20090000753 Vestola et al. Jan 2009 A1
20090001635 Newson et al. Jan 2009 A1
20090008275 Ferrari et al. Jan 2009 A1
20090117365 Mallory et al. May 2009 A1
20090131898 Malmgren et al. May 2009 A1
20090205794 Scherb et al. Aug 2009 A1
20090270005 Takahashi et al. Oct 2009 A1
20100006498 Duello Jan 2010 A1
20100075858 Davis et al. Mar 2010 A1
20100132144 Rautray Jun 2010 A1
20100136294 Manifold et al. Jun 2010 A1
20100251611 Henson Oct 2010 A1
20100273716 Harris Oct 2010 A1
20100327484 Schuh et al. Dec 2010 A1
20110045261 Sellars Feb 2011 A1
20120121674 Pedoja May 2012 A1
20120177888 Escafere et al. Jul 2012 A1
20130268062 Puckett et al. Oct 2013 A1
20140102650 Qin et al. Apr 2014 A1
20140189970 Fingal et al. Jul 2014 A1
20140231037 Beaupre et al. Aug 2014 A1
20140324007 Hundorf et al. Oct 2014 A1
20150080823 Thompson et al. Mar 2015 A1
20150144829 Grünbauer May 2015 A1
20150284911 Juvonen et al. Oct 2015 A1
20150330029 Ramaratnam Nov 2015 A1
20160160448 Miller, IV et al. Jun 2016 A1
20160219810 Erkkilä et al. Aug 2016 A1
20160353820 Baychar Dec 2016 A1
20170016149 Nakamura Jan 2017 A1
20170335521 Lee Nov 2017 A1
20170335522 Heiskanen et al. Nov 2017 A1
20170362775 Juvonen et al. Dec 2017 A1
20180119353 Tolfsson et al. May 2018 A1
20180140529 Miller, IV May 2018 A1
20180162107 Xu Jun 2018 A1
20180327973 Siitonen et al. Nov 2018 A1
20180355527 Strandqvist et al. Dec 2018 A1
20190161915 Swails et al. May 2019 A1
20200190739 Qin Jun 2020 A1
20200370246 Calewarts Nov 2020 A1
Foreign Referenced Citations (194)
Number Date Country
517303 Dec 2016 AT
519414 Jun 2018 AT
519423 Aug 2018 AT
281485 Feb 1965 AU
1973057198 Jan 1975 AU
700394 Jan 1999 AU
721197 Jun 2000 AU
2002300959 Jun 2003 AU
2001285005 Feb 2006 AU
2007272602 Jan 2008 AU
2012298266 Jun 2016 AU
436451 Sep 1939 BE
949706 Jun 1974 CA
979699 Dec 1975 CA
2194176 Dec 1996 CA
2868935 Sep 2014 CA
2998561 Mar 2018 CA
3044228 May 2018 CA
1173122 Feb 1998 CN
1260977 Jul 2000 CN
1270648 Oct 2000 CN
1364182 Aug 2002 CN
1094542 Nov 2002 CN
1518423 Aug 2004 CN
1529651 Sep 2004 CN
101300383 Nov 2008 CN
101443240 May 2009 CN
101453972 Jun 2009 CN
103068567 Apr 2013 CN
101410078 Feb 2014 CN
205000573 Jan 2016 CN
103993498 Mar 2016 CN
105828763 Aug 2016 CN
105828764 Aug 2016 CN
105899173 Aug 2016 CN
104302834 Nov 2016 CN
106456416 Feb 2017 CN
106988022 Jul 2017 CN
107460764 Dec 2017 CN
107988838 May 2018 CN
109937027 Jun 2019 CN
2041406 Apr 1971 DE
2438587 Mar 1975 DE
2902255 Jul 1980 DE
3307736 Sep 1984 DE
3420195 Jun 1987 DE
4207233 Nov 1993 DE
0101319 Mar 1984 EP
3049944 Nov 1984 EP
0264676 Apr 1988 EP
0136329 Jan 1989 EP
0158938 Dec 1989 EP
0296242 Jul 1991 EP
0443082 Aug 1991 EP
0242361 Sep 1991 EP
0512819 Nov 1992 EP
0150777 Nov 1994 EP
0481745 Jul 1996 EP
0537005 Jul 1997 EP
0671504 Aug 1997 EP
0742858 Jun 1999 EP
0951603 Aug 2002 EP
1007784 Feb 2003 EP
1145695 Jan 2004 EP
1194644 Mar 2004 EP
1457590 Sep 2004 EP
1400224 Mar 2006 EP
1384457 May 2006 EP
1808116 Jul 2007 EP
1649094 Sep 2007 EP
1442173 Mar 2008 EP
1583865 May 2008 EP
1463432 Aug 2008 EP
1576233 Oct 2008 EP
1813237 Dec 2008 EP
1932968 Sep 2009 EP
1967626 Sep 2009 EP
1666240 Mar 2011 EP
1440195 Aug 2011 EP
1812637 Jan 2012 EP
1950343 Apr 2012 EP
1456472 May 2012 EP
1497489 Aug 2012 EP
1808152 Aug 2012 EP
1567718 Apr 2013 EP
2599915 Jun 2013 EP
1268937 Feb 2014 EP
2540892 Apr 2014 EP
1876291 Sep 2014 EP
2843130 Mar 2015 EP
2952164 Dec 2015 EP
2952165 Dec 2015 EP
2737131 Jan 2016 EP
1916333 Jun 2016 EP
2001662 Jun 2016 EP
1380401 Jul 2016 EP
2807212 Apr 2017 EP
2940210 Aug 2017 EP
2622132 Apr 2018 EP
3327395 May 2018 EP
3162956 Mar 2019 EP
3108060 Apr 2021 EP
385106 Mar 1973 ES
8606100 Apr 1986 ES
2362723 Jul 2011 ES
812601 Feb 1982 FI
843904 Oct 1984 FI
83741 Dec 1992 FI
112812 Jan 2004 FI
127377 Apr 2018 FI
128917 Mar 2021 FI
873763 Jul 1942 FR
1449737 Aug 1966 FR
1528992 Jun 1968 FR
2206398 Sep 1976 FR
1145484 Mar 1969 GB
2109023 May 1983 GB
2136813 Sep 1984 GB
2116882 Oct 1985 GB
2582508 Sep 2020 GB
1182DEL2005 Jan 2007 IN
231170 Mar 2009 IN
2957KOLNP2014 May 2015 IN
3108MUM2014 Apr 2016 IN
283291 May 2017 IN
201717030330 Dec 2017 IN
201837033267 Oct 2018 IN
1983115199 Jul 1983 JP
1989501859 Jun 1989 JP
1993140886 Jun 1993 JP
4817935 Nov 2011 JP
1020040088545 Oct 2004 KR
100450272 Dec 2005 KR
100637646 Oct 2006 KR
100685522 Feb 2007 KR
100725240 Jun 2007 KR
1020100112299 Oct 2010 KR
1020130077856 Jul 2013 KR
101386319 Apr 2014 KR
1020180007337 Jan 2018 KR
2393093 Jun 2010 RU
7304825 Nov 1977 SE
7304888 Nov 1977 SE
412881 Mar 1980 SE
1651412 Apr 2018 SE
540719 Oct 2018 SE
1986003505 Jun 1986 WO
1991010416 Jul 1991 WO
1992003283 Mar 1992 WO
9314267 Jul 1993 WO
1996031652 Oct 1996 WO
2000001882 Jan 2000 WO
0025716 May 2000 WO
2000050694 Aug 2000 WO
0112902 Feb 2001 WO
2001068793 Sep 2001 WO
2001083866 Nov 2001 WO
2002055788 Jul 2002 WO
2003069038 Aug 2003 WO
2004025009 Mar 2004 WO
2004112956 Dec 2004 WO
2005060712 Jul 2005 WO
2006052967 May 2006 WO
2006094077 Sep 2006 WO
2007074625 Jul 2007 WO
2009006371 Jan 2009 WO
2009060118 May 2009 WO
2011104427 Sep 2011 WO
2014068196 May 2014 WO
2014080084 May 2014 WO
2014205048 Dec 2014 WO
2015083092 Jun 2015 WO
2015112155 Jul 2015 WO
2015173474 Nov 2015 WO
2016050901 Apr 2016 WO
2016051350 Apr 2016 WO
16122477 Aug 2016 WO
2016185398 Nov 2016 WO
2016200299 Dec 2016 WO
2017006216 Jan 2017 WO
2017006241 Jan 2017 WO
2017046751 Mar 2017 WO
2017079169 May 2017 WO
2017137879 Aug 2017 WO
2018002815 Jan 2018 WO
2018011667 Jan 2018 WO
2018041355 Mar 2018 WO
2018065668 Apr 2018 WO
2018116223 Jun 2018 WO
2018152082 Aug 2018 WO
2018171913 Sep 2018 WO
2018171914 Sep 2018 WO
WO-2018199975 Nov 2018 WO
WO-2019108172 Jun 2019 WO
Non-Patent Literature Citations (2)
Entry
Hubbe et al., in “Wet-Laid Nonwovens Manufacture Chemical Approaches Using Synthetic and Cellulosic Fibers” BioResources 11(2) pp. 5500-5552. (Year: 2016).
Vinda Paper (China) Co., Ltd, “Unbreakable in Water 3-layer Thickness Facial Tissue Paper”, Jun. 16, 2017, http://vinda.gmc.globalmarket.com/products/details/unbreakable-in-water-3-layer-thickness-facial-tissue-paper-10750223.html.
Related Publications (1)
Number Date Country
20200370246 A1 Nov 2020 US