Embodiments of the presently disclosed technology relate to new and improved flooring planks, wall coverings, or other decorative panels, and more particularly flooring planks, wall coverings, or other decorative panels comprising a melamine-impregnated protective layer bonded to a composite core, such as a plastic composite core or a mineral composite core.
Ceramic or porcelain tiles and planks are widely used as floor coverings because of their waterproof properties and superior surface durability. However, one disadvantage of traditional ceramic or porcelain tiles and planks is installation often takes several days and can be a messy process due to the use of adhesive, mortar, and grout. Satisfactory installation often requires a competent professional installer and the removal process can be very disruptive and costly.
While there have been attempts to simplify the installation method for ceramic and porcelain tiles and planks, such as that described in U.S. Pat. No. 8,631,624, experience in the field has demonstrated that those products are not performing satisfactorily. Generally, such alternate methods require installing the ceramic tiles without the use of glue and often without grout as well; however, ceramic tiles produced using these methods tend to be brittle and crack over time over, especially if installed over an uneven subfloor.
The disadvantages described above are among the reasons why thermoplastic-based or polymer-based flooring, and particularly polyvinylchloride flooring, are greatly appreciated by the end user. Several types of thermoplastic flooring already exist on the market, such as products commonly known as vinyl flooring, LVP/LVT flooring, WPC, and the like. Such types of flooring bring additional features such as higher rigidity, sound reduction, and better footstep comfort when compared to ceramic or porcelain tiles in addition to waterproofing and ease of assembly.
The visual appeal of thermoplastic-based alternatives to ceramic and porcelain tiles has been improved by use of embossed-in-register technology, deeper beveling, the use of high-resolution printed images, and efforts to lower gloss, but almost all thermoplastic flooring products on the market continue to use a plastic-based protective layer. This protective layer is generally made of polyvinyl chloride, but some alternative protective layers are made utilizing polyethylene terephthalate, polyurethane, or polypropylene. The core, décor layer, and the protective layer are generally made of the same type of polymer and fused together through a thermo-bonding process.
Plastic protective layers can be unattractive. Indeed, when a plastic protective layer is employed, the surface of the finished product tends to have a slightly dull appearance and what is commonly called in the flooring industry a “plastic look.” In contrast, ceramic and porcelain tiles are said to have a much more aesthetically pleasing, “natural” appearance.
To improve the surface durability of those thermoplastic-based flooring products, a finish is generally applied on top of the plastic protective layer. This finish is, in most cases, a urethane coating which comprises corundum, silicone dioxide particles, ceramic beam, or diamond particles. However, the effects of such coatings are limited, and only serve to slightly improve the micro-scratch resistance of the surface.
Thus, there remains a need for an improved flooring product that is substantially waterproof, easy to install, has improved scratch resistance, yet presents a durable and pleasing “natural” look and feel. Likewise, there remains a need for a process by which such an improved flooring product may be easily and inexpensively manufactured. Embodiments of the presently disclosed technology are directed to these and other considerations.
Embodiments of the presently disclosed technology include a panel comprising a protective layer formed of a paper impregnated with a melamine resin, a décor layer comprising a thermoplastic film, the décor layer disposed below the protective layer, an adhesive layer bonding an upper surface of the décor layer to a lower surface of the protective layer, and a rigid core comprising a primary component and a secondary component and disposed below the décor layer.
In some embodiments, the protective layer can comprise abrasion-resistant particles (e.g., aluminum oxide, silicon dioxide, ceramic beam, diamond particles, or a combination thereof).
In some embodiments, the protective layer is substantially transparent. In some embodiments, the protective layer has a weight of from 30 g/m2 to about 150 g/m2.
In some embodiments, wherein the thermoplastic film of the décor layer is selected from the group consisting of poly-vinyl chloride, polyethylene, polypropylene, polyurethane, or a combination thereof. In some embodiments, the décor layer is laminated to an upper surface of the core.
In some embodiments, the primary component of the core comprises one of a thermoplastic or an inorganic compound and the secondary component comprises calcium carbonate, kaolin, wallasonite, calcium silicate, or a combination thereof. In some embodiments, the core further comprises wood fibers in the amount of 30% or less by weight of the core. In some embodiments, the core comprises about 25% to about 45% polyvinylchloride and from about 45% to about 65% calcium carbonate. In some embodiments, the core comprises about 40% to about 55% magnesium oxide and about 20% to about 25% magnesium salt, such as magnesium chloride or magnesium sulfate.
In some embodiments, the panel has a deep scratch resistance as measured by ISO 1518 of 20N to 30N.
In some embodiments, the panel further comprises an edge locking system.
Embodiments of the presently disclosed technology include a panel comprising a protective layer comprising a paper impregnated with a melamine resin and an adhesive, the melamine resin further comprising abrasion-resistant particles; a décor layer comprising a thermoplastic film, the décor layer disposed below and bonded to the protective layer; and a rigid core layer, the rigid core layer comprising a primary component and a secondary component and disposed below the décor layer.
In some embodiments, wherein the protective layer comprises a top surface of the panel, and has a top surface having a hardness of at least 70 shore D.
In some embodiments, the adhesive is selected from the group of polyurethane, polyester, polyethylene, ethyl vinyl acetate, nylon, polyolefin, polyvinyl acetate, acrylic, urethan. In some embodiments, the adhesive is a melted film.
In some embodiments, the core can be produced by extrusion, calendaring, continuous process or a combination of these.
Embodiments of the presently disclosed technology include a panel comprising a protective layer formed of a decor paper impregnated with a melamine resin, an adhesive layer bonding an upper surface of the core to a lower surface of the protective layer, and a rigid core layer comprising a primary component and a secondary component and disposed below the protective layer.
The particular features and advantages of the presently disclosed technology as well as other objects will become apparent from the following description taken in connection with the accompanying drawings in which:
Embodiments of the presently disclosed technology include new and improved flooring planks, wall coverings, or decorative panels comprising a melamine-impregnated protective layer bonded to a composite core.
As used throughout this disclosure, the term “panel” is intended to reference some or all of at least flooring planks, wall coverings, or other decorative panels and is not intended to limit the scope of this disclosure. Normal usage of the presently disclosed panels may occur in a variety of locations including, but not limited to, residences (e.g., living areas, bathrooms, kitchens, basements), commercial spaces, offices, gyms, studios, or stores. While reference throughout this disclosure is made expressly to panels, it is understood that the embodiments of the present disclosure may be useful in other applications.
As used herein, a “plastic composite core” may refer to a core having a plastic component and an inorganic component. In some embodiments, the composite core may comprise at least 20% by weight of a plastic (e.g., polyvinyl chloride (PVC), polyethylene (PE), polyethylene terephthalate (PET), polyurethane (PU), ethylene vinyl acetate (EVA), ABS, and polypropylene (PP)), and a filler (e.g. calcium carbonate, kaolin, wallasonite, calcium silicate, or a combination thereof). It is understood that the type of filler and plastic can vary greatly depending on design needs. The inorganic component may comprise fiber cement, gypsum, plaster, magnesium oxide, or other cements or concretes, such as magnesium oxychloride cements. As used herein, a “mineral composite core” includes an inorganic compound and a filler. In embodiments where the composite core is a mineral composite core, the composite core may contain about 0 to 30% by weight of wood fibers and in an example embodiment, about 8% by weight of wood fibers.
In the past, it has been challenging to use a protective layer including melamine resin on top of a non-wood-based core, such as a composite core (e.g., a primarily polymer-based or mineral-based core having less than about 20% by weight of wood fibers) because:
Some attempts have been made to use a melamine resin protective layer on top of a polymer-based core, such as described in U.S. Pat. Nos. 9,611,659 and 9,745,758. However, in those patents, the top layer comprises several layers of impregnated paper (commonly called “HPL” or “High Pressure Laminate”). The use of HPL makes the fabrication process slow and expensive. Additionally, both during the manufacturing process and as a finished product, HPLs are known to undergo significant structural changes in reaction to changes in the environment, such as changes in temperature and/or humidity, due to the relatively large quantity of resin and paper used in those processes.
Embodiments of the presently disclosed technology include a panel with high surface durability with a natural look and feel, and a core suitable to be profiled with a locking system to make installation and disassembly easy, fast, and clean. For instance, the panels show increased durability through surface micro-scratch resistance, deep scratch resistance, and heat resistance. Due to the manufacturing processes discussed below, it is possible to manufacture a panel with a composite core and having a single layer of melamine-impregnated paper as a protective layer. As discussed in more detail below, in some embodiments, the protective layer may include embossing to provide texture to the plank and provide a natural look and feel.
As used herein, the term “protective layer” may refer to a layer providing protection against wear caused by normal usage of the planks, including but not limited to abrasion-resistance, scratch-resistance, and/or water-proofing. In some embodiments, the protective layer can comprise a paper impregnated with melamine resin. In other embodiments, the protective layer can be a combined décor layer and protective layer, in which a décor layer is impregnated with melamine resin. In some embodiments, the paper or décor layer can be impregnated with the melamine resin by the manufacturing processes described in
In some embodiments, the paper used in the protective layer can be a transparent paper. In some embodiments, the paper can have a weight of from 15 g/m2 to 70 g/m2, and more specifically from 45 g/m2 to 58 g/m2. In some embodiments, the paper can be impregnated with a melamine resin such that the final weight of the protective layer can be from 30 g/m2 to 150 g/m2 depending on the starting weight of the paper. After impregnation with the resin, the protective layer can be substantially transparent due to the transparency of the resin, the thinness and weight of the paper, and the amount of cellulose fibers contained in the paper.
In embodiments utilizing a combined décor layer and protective layer, the décor layer can comprise a décor paper having a weight of from 60 g/m2 to 80 g/m2 and in an example embodiment, a weight of around 75 g/m2. In some embodiments, the décor paper can be impregnated with a melamine resin in an amount of about 1 to 3 times the paper weight.
In some embodiments, the protective layer may additionally comprise abrasion-resistant particles (e.g., aluminum oxide, silicon dioxide, ceramic beam, and diamond particles) that may resist wear and tear during normal usage of the panels. In embodiments where abrasion-resistant particles are used, the protective layer can contain from about 15 g/m2 to about 100 g/m2 abrasion-resistant particles. In some embodiments, the protective layer can contain from about 20 g/m2 to about 50 g/m2 abrasion-resistant particles, about 25 g/m2 to about 50 g/m2 abrasion-resistant particles, about 30 g/m2 to about 50 g/m2 abrasion-resistant particles, about 40 g/m2 to about 50 g/m2 abrasion-resistant particles.
In embodiments incorporating a separate décor layer, to improve the clarity of the décor layer beneath, it may be preferable to use a lightweight paper having relatively less cellulosic fibers to be more transparent. However, lighter-weight papers contain less hard or abrasion-resistant particles diminishing the wear and scratch-resistance of the finished product. Thus, in an example embodiment incorporating a lighter-weight paper (e.g., a paper having a weight of about 25 g/m2), a polyurethane adhesive containing hard particles can be used to bond the décor layer to the core. Those skilled in the art would understand that the protective layer can be substantially transparent because it is made of a thin paper and the resin used is transparent.
The protective layer can be bonded either directly or indirectly to the core. In some embodiments, the protective layer may be bonded to an additional layer (e.g., a décor layer or an upper sublayer). For instance, the protective layer can be bonded using an adhesive (e.g., PU, polyester, PE, EVA, nylon, polyolefin, PVA, acrylic, urethane). In some embodiments, the protective layer can be bonded to the core via a lamination process, such as cold or hot pressing.
In some embodiments, the panels can comprise a composite core such as a plastic composite core or a mineral composite core. For instance, the core can comprise a primary component and a secondary component. In embodiments comprising a plastic composite core, the primary component can be a thermoplastic material. Suitable thermoplastic materials can include PVC, PP, PE, EVA, PET, PU, or a combination thereof. In embodiments where the core is a mineral composite core, the primary component may be a mineral-based material. Suitable mineral-based materials can include calcium silicate, fiber cement, magnesium oxide, gypsum, fired or unfired clay, or a combination thereof. In some embodiments, the primary component can be present in an amount of from about 10 to about 30% by weight, about 10 to about 15% by weight, about 15 to about 20% by weight, about 20% to about 25% by weight, and about 25% to about 30% by weight.
In some embodiments, the secondary component can be a filler, such as calcium carbonate, kaolin, wallasonite, calcium silicate, fly ash, or a combination thereof. In some embodiments, the secondary component can be present in an amount of from about 30 to about 70% by weight, about 35% to about 65% by weight, about 40% to about 60% by weight, about 45% to about 55% by weight, and about 50% to about 65% by weight.
In some embodiments, the core can comprise a minimal amount of wood-based component in an amount of from about 0% to about 30%, about 5% to about 10%, about 10% to about 30%, about 15% to about 20%, or about 20% to about 30%. The wood-based material may comprise any type of wood or natural fibers known in the art. In accordance with the above, example raw material makeups (excluding additional additives) of the core compositions are shown in Table 1 below.
In an example embodiment, the plastic composite core can be a highly-filled, rigid PVC core. A highly-filled core can comprise a percent by weight of filler that is at least double that of the percent by weight of PVC. For instance, the amount of filler can be approximately 65% by weight of the core and the amount of thermoplastic can be 25% by weight of the core (e.g., 65% CaCo3 and 25% PVC). As used herein, “rigid” may refer to a core that is substantially free of a plasticizer or other flexibility-imparting material.
A core such as this may be produced by a variety of different techniques, such as extrusion, co-extrusion, hot press, calendaring, or continuous press.
The core of the present invention can be solid or foamed.
The thermoplastic composite core of the present invention may be made of one layer or a plurality of layers.
In some embodiments, the core may comprise other additives such as foaming agents, heat stabilizers, wax, and impact modifiers to adjust other properties of the core.
In other embodiments, the core may be a mineral composite core. A mineral composite core may be a core that includes a primary component comprised of an inorganic compound and a secondary component comprised of a filler. For instance, in some embodiments, the primary component may be magnesium oxide. In other embodiments, the primary component may be calcium silicate, fiber cement, magnesium oxide, gypsum, perlite, fired or unfired clay, magnesium chloride, or a combination thereof. In some embodiments, the composite mineral core may comprise one or more additional components comprised of one or more of a filler, an additive, a foaming agent, a binder, such as wood fibers, or a reinforcing component, such as a fiberglass board or fiberglass fibers. In some embodiments, the composite mineral core may comprise a secondary component comprising a magnesium salt, such as magnesium chloride or magnesium sulfate.
In some embodiments, the density of the core may be varied depending on the application. For example, for a flooring application, the density of the mineral composite core can be between about 1200 kg/m2 to about 1500 kg/m2. In contrast, for a wall application, a lighter density core is preferred, such as a mineral composite core having a density of about 800 kg/m2 to about 1200 kg/m2. As used herein, the density of the board may refer to the calculation of dividing the weight of the specimen by the volume of the specimen (width×thickness×length).
Various methods are known in the art to adjust the density of the mineral composite core. For instance, in some embodiments, a lightweight filler (e.g., perlite) or polystyrene may be added. In other embodiments, the fiber content may be increased (e.g., to 40% or less of wood fibers) or a foaming agent (e.g., sodium bicarbonate or azodicarbonamide) may be used. Additionally, in some embodiments, natural fibers, such as cellulose, wood fibers, or bamboo fibers, or cork particles may be incorporated to increase flexibility. Natural fibers within the core can also be incorporated to improve the strength of the locking system. In some embodiments, the mineral composite core can comprise from about 3% to about 15% by weight of natural fibers. Depending on the type of inorganic compound used, the mineral composite core may be too brittle for use, so a reinforcing material can be used to impart additional strength and flexibility to the board. In some embodiments, one or more fiberglass mesh layers may be used to strengthen the core.
In some embodiments, the mineral composite core can additionally include a binder. The type of binder can be important for providing adequate locking strength for the locking system mating protrusions and receptacles. In some embodiments, the binder may be magnesium sulfate, magnesium chloride, or a combination thereof. To provide a suitable substrate for a flooring material, the binder content used therein can be 50% by weight or less. Table 2 illustrates example embodiments of the core composition comprising magnesium oxide:
In some embodiments, the core can be waterproof. The core can be solid or foamed.
Embodiments of the presently disclosed panels exhibit improved scratch resistance as compared to currently-available thermoplastic core products (e.g., SPC, WPC and RCB).
For instance, panels as provided by the present disclosure (e.g., Table 1 and Table 2) were tested using the Laminate Floor Coverings—Test Method For The Determination of Micro-Scratch Resistance, EN 16094 (2012), procedure B, which requires a sample surface be checked for scratches after 160 revolutions of a Martindale test machine. As compared to SPC, WPC, and RCB products on the market, which exhibited notable scratching after 160 revolutions, panels of the present disclosure can endure between 200 and 10,000 revolutions before exhibiting noticeable scratches, as exhibited in Table 3.
Additionally, as exhibited in Table 3, panels of the present disclosure show improved deep scratch resistance when tested according to ISO 1518.
The presently disclosed panels also have improved heat resistance as demonstrated by the “cigarette burn test method” described in EN 438-2. When tested via EN 438-2, the described panels have no mark or slight marking due to a cigarette burn whereas traditional vinyl, SPC or WPC flooring show a moderate to severe mark.
In some embodiments, the core can be waterproof and structurally rigid enough to be profiled with a glueless locking system.
In some embodiments, the adhesive selected to be combined with the melamine resin has a high transparency when applied over the décor layer. Transparency of the adhesive can be measured by applying the adhesive on a uniform white film and then measuring the color difference (Δa, Δb, Δc, ΔE) between the areas with the adhesive and without the adhesive using, for instance a spectrophotometer. Ideally the ΔE is less than 1 after application of the adhesive. In some embodiments, the adhesive is heat-resistant from at least 130° C. and up to about 200° C.
In some embodiments, a polyurethane adhesive resin (resistant to temperature up to about) 200° C. can be used to reduce the pressing time. In some embodiments, the polyurethane adhesive resin is water-based to dry quickly to facilitate packaging of the panels at the end of the manufacturing process.
As discussed in more detail below with respect to
Turning now to the figures where various example embodiments of panels are illustrated and reference numerals are used to refer to certain components of the depicted panels, the embodiments illustrated in the figures are merely example embodiments and are not intended to limit this disclosure. The various components of the panels illustrated in the figures may have some or all of the features described above.
Adhesive layer 11 is positioned between protective layer 1 and décor layer 2 forming a bond between protective layer 1 and décor layer 2. An optional balancing layer 4 is shown in
In some embodiments, sublayers 7 and 8 shown in
As with previous embodiments, panel 40 may further comprise a balance layer 46.
Bonding a virtually transparent thermoplastic layer 77 between décor layer 72 and protective layer 71 allows the use of a lighter melamine-impregnated paper as protective layer 71 and balancing layer 74, which helps to improve the dimensional stability of the product. In this case, the melamine-impregnated paper used as protective layer 71 has a weight of between about 10 g/m2 to about 35 g/m2 and, in an example embodiment, of about 20 g/m2. The weight of the paper of the balancing layer 74 can be from about 10 g/m2 to about 140 g/m2, and in an example embodiment, about 90 g/m2. Incorporating a lightweight melamine impregnated paper as the protective layer provides superior scratch resistance. In some embodiments, a virtually transparent thermoplastic layer 77 may be included to improve wear resistance. In some embodiments, the virtually transparent thermoplastic layer 77 may comprise a transparent PVC wear layer. The thickness of the virtually transparent thermoplastic layer 77 can vary from about 0.1 mm to about 0.7 mm and in some embodiments is about 0.3 mm.
In some embodiments, the impregnated paper can be applied to the core using a hot press process. There are 3 types of hot press processes that may be used to apply the paper to the core: single daylight hot press, multilayer process, and continuous press. In embodiments incorporating a multilayer hot process, multiple layers (e.g., wear layer, protective layer, décor layer, and core layer) intended to be pressed together are sandwiched between two plates. Once all the layers are loaded on the plates, the press is closed and heat is added to each plate. A pressure of 8 MPa to 18 Mpa can be used during the heat phase at a temperature of around 40° C. for about 20 minutes.
In embodiments incorporating a single daylight press, layers are positioned between two plates and the press is closed. The plates are pressed together at a pressure of between 16 and 21 MPa at a temperature of around 190° C. for about one minute. In embodiments incorporating a continuous press, layers are positioned between two conveyer belts that are heated and caused to apply a continuous pressure on the layers.
Another example method 850, shown in
Another method of applying the polyurethane adhesive to create a panel according to the present invention is illustrated in
In some embodiments, when several layers are applied, it is possible to add urethane resin as well to improve the application process to reduce the tackiness of the surface and improve the adhesion of the various layers.
Another advantage of the present disclosure is that improved 3D texturing can be used to improve the appearance of the panels. Another pair of related prior patents, U.S. Pat. No. 7,763,345 (the “'345 Patent”) and European Patent No. 2248665 (the “'665 Patent”), describe an aminoplast resin top layer, but the aminoplast material is again an HPL layer. HPL was used by the owner of these patents several years ago to make a flooring product, but that product quickly disappeared from the market because of the complexity and high cost of the process. The product described in the '345 and '665 Patents has an HPL top layer and a thermoplastic core, the HPL top layer is produced separately first as a separate sheet and completely cured. Subsequently, the top layer is pressed on top of the core. The depth of 3D texturing of the surface of products produced according to the '345 and '665 Patents is limited to the thickness of the HPL itself. 3D texturing cannot extend into the core of products produced according to these prior art patents because the protective layer is separately produced and cured before being applied to the core. In the present invention, there is no need for this first separate process and therefore 3D texturing can extend into the core of the products.
A cross-sectional view of the prior art panel produced according to the '345 and '665 Patents, is illustrated in
In contrast,
As used herein, the term “décor layer” may refer to a layer providing a decorative effect to a plank but also providing protection against wear caused by normal usage of the planks, including but not limited to abrasion-resistance, scratch-resistance, and/or water-proofing. The decorative effect can comprise a printed motif illustrative of a type of flooring décor (e.g. hardwood, tile, stone etc.). The decorative effect may be provided by one or more processes including rotogravure or digital print technology.
Numerous alterations of the structure herein disclosed will suggest themselves to those skilled in the art. However, it is to be understood that the present disclosure relates to the preferred embodiment of the invention which is for purposes of illustration only and not to be construed as a limitation of the invention. All such modifications which do not depart from the spirit of the invention are intended to be included within the scope of the appended claims.
This application titled “Composite Panels Having a Melamine Impregnated Paper Wear Layer” is a non-provisional application claiming the benefit to Provisional Application No. 62/735,607 filed Sep. 24, 2018 and titled “Solid Polymer-Based or Mineral-Based Core Flooring and Wall Panel Having Melamine Impregnated Paper Wear layer,” which is hereby incorporated by reference in its entirety as if set forth below.
Number | Name | Date | Kind |
---|---|---|---|
795399 | Laybrun | Jul 1905 | A |
2182291 | Andre | Dec 1939 | A |
3908725 | Koch | Sep 1975 | A |
4724187 | Ungar | Feb 1988 | A |
6146252 | Martensson | Nov 2000 | A |
6248812 | Symons | Jun 2001 | B1 |
6440538 | Ungar | Aug 2002 | B1 |
6617009 | Chen | Sep 2003 | B1 |
6986934 | Chen | Jan 2006 | B2 |
7155871 | Stone | Jan 2007 | B1 |
7169460 | Chen | Jan 2007 | B1 |
7211310 | Chen | May 2007 | B2 |
7220297 | Pipko | May 2007 | B2 |
7261947 | Reichwein | Aug 2007 | B2 |
7419717 | Chen | Sep 2008 | B2 |
7527856 | Thiers | May 2009 | B2 |
7544423 | Horton | Jun 2009 | B2 |
7678425 | Oldorff | Mar 2010 | B2 |
7763345 | Chen | Jul 2010 | B2 |
7770350 | Moriau | Aug 2010 | B2 |
7866115 | Pervan | Jan 2011 | B2 |
7877956 | Martensson | Feb 2011 | B2 |
7998547 | Feigin | Aug 2011 | B2 |
8021741 | Chen | Sep 2011 | B2 |
8099919 | Garcia | Jan 2012 | B2 |
8171691 | Stone | May 2012 | B1 |
8234829 | Thiers | Aug 2012 | B2 |
8431054 | Pervan | Apr 2013 | B2 |
8631624 | McIntosh | Jan 2014 | B2 |
8834992 | Chen | Sep 2014 | B2 |
8875465 | Martensson | Nov 2014 | B2 |
9745758 | Baert | Aug 2017 | B2 |
9783996 | Pervan | Oct 2017 | B2 |
9994010 | Pervan | Jun 2018 | B2 |
20010007710 | Liu | Jul 2001 | A1 |
20020025446 | Chen | Feb 2002 | A1 |
20020046527 | Nelson | Apr 2002 | A1 |
20030024199 | Pervan | Feb 2003 | A1 |
20040016196 | Pervan | Jan 2004 | A1 |
20040086678 | Chen | May 2004 | A1 |
20040200154 | Hunter | Oct 2004 | A1 |
20040248489 | Hutchison | Dec 2004 | A1 |
20040255538 | Ruhdorfer | Dec 2004 | A1 |
20050003160 | Chen | Jan 2005 | A1 |
20050136234 | Hak | Jun 2005 | A1 |
20050176321 | Crette | Aug 2005 | A1 |
20050281997 | Grah | Dec 2005 | A1 |
20060032175 | Chen | Feb 2006 | A1 |
20060070321 | Au | Apr 2006 | A1 |
20070130872 | Goodwin | Jun 2007 | A1 |
20080261019 | Xianfeng | Oct 2008 | A1 |
20090011670 | Wisenbaker | Jan 2009 | A1 |
20100247937 | Liu et al. | Sep 2010 | A1 |
20110167744 | Whispell | Jul 2011 | A1 |
20110247285 | Wybo | Oct 2011 | A1 |
20110300392 | Vermeulen | Dec 2011 | A1 |
20130171377 | Aravamudan | Jul 2013 | A1 |
20130192158 | Cappelle | Aug 2013 | A1 |
20140290158 | Meersseman | Oct 2014 | A1 |
20140356594 | Chen | Dec 2014 | A1 |
20150159379 | Meersseman | Jun 2015 | A1 |
20150167320 | Meersseman | Jun 2015 | A1 |
20150290968 | Hannig | Oct 2015 | A1 |
20160083965 | Baert | Mar 2016 | A1 |
20160369507 | Pervan | Dec 2016 | A1 |
20170298639 | Song | Oct 2017 | A1 |
20180171631 | Klug | Jun 2018 | A1 |
20180258650 | Meersseman | Sep 2018 | A1 |
20180291638 | Pervan | Oct 2018 | A1 |
20190010711 | Pervan | Jan 2019 | A1 |
Number | Date | Country |
---|---|---|
2852656 | Apr 2013 | CA |
1043279 | Dec 1989 | CN |
1052819 | Jul 1991 | CN |
2193915 | Apr 1995 | CN |
1113850 | Dec 1995 | CN |
1118771 | Mar 1996 | CN |
1189566 | Aug 1998 | CN |
1194202 | Sep 1998 | CN |
1245855 | Mar 2000 | CN |
1446993 | Oct 2003 | CN |
1482166 | Mar 2004 | CN |
2642917 | Sep 2004 | CN |
1656291 | Aug 2005 | CN |
2765969 | Mar 2006 | CN |
1792986 | Jun 2006 | CN |
1850712 | Oct 2006 | CN |
1911997 | Feb 2007 | CN |
2880871 | Mar 2007 | CN |
101003990 | Jul 2007 | CN |
101042014 | Sep 2007 | CN |
101115616 | Jan 2008 | CN |
200720034739.X | Jan 2008 | CN |
ZL 200620075187.2 | Feb 2008 | CN |
101173554 | May 2008 | CN |
201071580 | Jun 2008 | CN |
201128262 | Oct 2008 | CN |
101323188 | Dec 2008 | CN |
101367977 | Feb 2009 | CN |
1004623981 | Feb 2009 | CN |
101386516 | Mar 2009 | CN |
201209309 | Mar 2009 | CN |
101423349 | May 2009 | CN |
101446128 | Jun 2009 | CN |
1101487336 | Jul 2009 | CN |
101545309 | Sep 2009 | CN |
101564922 | Oct 2009 | CN |
201339298 | Nov 2009 | CN |
101614068 | Dec 2009 | CN |
101767362 | Jul 2010 | CN |
201539080 | Aug 2010 | CN |
101487336 | Oct 2010 | CN |
201679203 | Dec 2010 | CN |
202023326 | Dec 2010 | CN |
202023326 | Dec 2010 | CN |
101955614 | Jan 2011 | CN |
101613503 | May 2011 | CN |
101698749 | Oct 2011 | CN |
102245690 | Nov 2011 | CN |
102287038 | Dec 2011 | CN |
202265980 | Jun 2012 | CN |
20232451 | Jul 2012 | CN |
201120467334 | Jul 2012 | CN |
201120467683 | Jul 2012 | CN |
202483139 | Oct 2012 | CN |
102803177 | Nov 2012 | CN |
107165376 | Sep 2017 | CN |
207144220 | Mar 2018 | CN |
202017100592 | May 2017 | DE |
2060389 | May 2009 | EP |
2202056 | Jun 2010 | EP |
2263867 | Mar 2012 | EP |
2248665 | Sep 2016 | EP |
2268547 | Mar 2007 | ES |
114462 | Oct 2004 | FI |
518239 | Feb 1940 | GB |
671731 | Oct 1994 | JP |
7223856 | Aug 1995 | JP |
2000054528 | Feb 2000 | JP |
2000297496 | Oct 2000 | JP |
2000303394 | Oct 2000 | JP |
2001140401 | May 2001 | JP |
2002274928 | Sep 2002 | JP |
2009132078 | Jun 2009 | JP |
5839097 | Jan 2016 | JP |
100710919 | Apr 2007 | KR |
20110045402 | May 2011 | KR |
20130077823 | Jul 2013 | KR |
2081135 | Jun 1997 | RU |
2329362 | Jul 2008 | RU |
2379249 | Jan 2010 | RU |
2001083888 | Nov 2001 | WO |
2001085642 | Nov 2001 | WO |
2001094716 | Dec 2001 | WO |
2006084513 | Aug 2006 | WO |
2010081860 | Jul 2010 | WO |
2012061300 | May 2012 | WO |
2017072657 | May 2017 | WO |
2018034614 | Feb 2018 | WO |
WO-2018068197 | Apr 2018 | WO |
2018234561 | Dec 2018 | WO |
Entry |
---|
Lauefenberg, Theodore L. et al., Phosphate-Bonded Ceramic-Wood Composites: R&D Project Overview and Invitation to Participate (Oct. 2004). |
Suzhou Mango New Building Materials Co., Ltd, Water Resistant HPL Veneer Laminated Mgo Board for Exterior Wall (2008). |
Aqua-Step; Promotional Website, Internet, Allegedly Nov. 24, 2009. |
Machine Translation of CN 201539080 U (Year: 2015). |
Number | Date | Country | |
---|---|---|---|
62735607 | Sep 2018 | US |