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    • 专利摘要:
    cellulose-based composite materials. a composite article based on cellulose mano-material and foam article is provided.
    公开号:BR112013005537B1
    申请号:R112013005537-5
    申请日:2011-09-07
    公开日:2021-04-13
    发明作者:Shoseyov Oded；Heyman Arnon；Lapidot Shaul；Nevo Yuval；Gustafsson Tord；Meirovitch Sigal
    申请人:Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd；
    IPC主号:
    专利说明:

    FIELD OF THE INVENTION
    The present invention is generally directed to cellulose foams and high strength composite materials comprising cellulose and a polymeric material. The invention is also directed to its applications as a core and / or structural materials. BACKGROUND OF THE INVENTION
    Cellulose is a polysaccharide with a linear chain of several hundred to more than ten thousand D-glucose units linked by β (1 ^ 4). Cellulose is a component of the primary cell wall structure of green plants, many forms of algae and oomycetes. Cellulose is also the main component of wood, and thus of paper, and is the organic compound on Earth. About 33% of all plant material is cellulose (the cellulose content of cotton is 90% and that of wood is 40-50%). Cellulose whiskers (CW) also known as nano crystalline cellulose (NCC) are fibers produced from cellulose; NCCs are typically single crystals of high purity. They constitute a generic class of materials with mechanical resistances equivalent to the binding forces of adjacent atoms. The resulting highly ordered structure produces not only unusual high resistances, but also significant changes in electrical, optical, magnetic, ferromagnetic, dielectric, conductive and even superconducting properties. The stress-resistant properties of NCC are far above those of today's high-volume reinforcements and allow the processing of the highest-strength composites obtainable. A review of the literature on NCC, its properties, and its possibility of use as a reinforcement phase in nano-composite applications as provided in [1-3].
    Another type of nano-cellulosic material are nano-fibers, known as Micro Fibrillated Cellulose (MFC) or Nano Fibrillated Cellulose (NFC), which are produced, for example, by enzymatic treatment of essentially bleached pulp followed by shearing and homogenization of essentially pulp bleached. In some cases, enzymatic pretreatments are applied in order to reduce the required production energy. Due to the relatively mild conditions employed, the amorphous cellulose remains intact, resulting in fibers of micrometric length with a nanometric diameter [4].
    Bacterial cellulose (BC) is a nano-structured extracellular product obtained from certain cellulose-producing bacteria such as Gluconobacter xilinus [5]. Cellulose fibrils, generally being of higher crystallinity and purity than those obtained from plant sources (insofar as no lignin or hemicellulose is present), are inherently of nano dimensions in their cross section.
    Polymeric foams are materials of high importance in the field of composite materials. Foams are used for many applications, for example, for insulation, structural parts such as car panels, as well as for core materials in the manufacture of sandwich composite panels for high strength, energy dissipation, insulation, and weight reduction . Conventional foams are produced from oil-based polymers such as polyvinyl chloride foam (PVC), polyethylene (PE), polyurethane (PU), polystyrene (PS), polymethacrylimide (PMI) and polypropylene (PP). Polymeric foams provide high insulation and weight reduction properties; however, some have low resistance and since they are all based on fossil oil, they represent a clear environmental disadvantage.
    Recently, it has been shown that NCC, as well as nano-fibers, can be processed into foams by simple methods. The preferred method for producing such foams is by molding NCC or nano-fiber suspension into molds followed by lyophilization. Foams can also be produced by any other foaming technique, such as extraction with supercritical fluid, microfluidics, etc. The resulting foams, also called aerogels, are highly porous and of low weight. However, these foams have low resistance to compression and, for this reason, their use as core materials is limited [3].
    NCCs have been shown to significantly increase the mechanical properties of polymeric composite materials. However, in order to obtain a homogeneous suspension of NCC in a polymeric resin, high energy and often expensive equipment is necessary [6]. Pranger and Tannenbaum [7] demonstrated that furan resin can be applied by cellulose nano-fibrils treated with dry sulfur and serves as a catalyst for furan polymerization. REFERENCES
    [1] De Souza Lima, M. and R. Borsali, Rodlike cellullose microcrystals: Structure, properties, and applications. Macromolecular Rapid Communications, 2004. 25 (7). [2] Samir, M., F. Alloin, and A. Dufresne, Review of recent research into cellulosic whiskers, their properties and their application in nanocomposite field. Biomacromolecules, 2005. 6 (2): pg. 612-626. [3] Eichhorn, S., et al., Review: current international research into cellullose nanofibers and nanocomposites. Journal of Materials Science. 45 (1): pg. 1-33. [4] Paakko, M., et al., Long and entangled native cellullose I nanofibers allow flexible aerogels and hierarchically porous templates for functionalities. Soft Matter, 2008. 4 (12): pg. 2492-2499. [5] Ross, P., et al., Celullose biosynthesis and function in bacteria. Microbiol. Rev., 1991. 55 (1): 35-58. [6] Oksman, K., D. Bondeson, and P. Syre, Nanocomposites Based On Celullose Whiskers and Celullose Plastics. 2006, US Patent Application No. 2008/0108772 [7] Pranger, L. and R. Tannenbaum, Biobased Nanocomposites Prepared by In Situ Polymerization of Furfurilic Alcohol with Celullose Whiskers or Montmorillonite Clay. Macromolecules, 2008. 41 (22): pg. 8682-8687. [8] Bondeson D, Mathew A, Oksman K: Optimization of the isolation of nanocrystals from microcrystalline cellullose by acid hydrolysis. Celullose 2006, 13 (2): 171-180. [9] Svagan AJ, Samir MAS, Berglund LA: Biomimetic foams of high mechanical performance based on nanostructured cell walls reinforced by native celullose nanofibrils. Advanced Materials 2008, 20 (7): 1263-1269. [10] Blaker JJ, Lee KY, Li X, Menner A, Bismarck A: Renewable nanocomposite polymer foams synthesized from Pickering emulsion templates. Green Chemistry 2009, 11 (9): 1321-1326. [11] Li Y, Ren H, Ragauskas AJ: Rigid polyurethane foam reinforced with celullose whiskers: Synthesis and characterization. Nano-Micro Letters 2010, 2 (2): 89-94. [12] Capadona J, Shanmuganathan K, Tyler D, Rowan S, Weder C: Stimuli-responsive polymer nanocomposites inspired by the sea cucumber dermis. Science 2008, 319 (5868): 1370. SUMMARY OF THE INVENTION
    The inventors of the present invention have developed a process for the preparation of foam materials from cellulose nanomaterials. Foam materials provide the opportunity to manufacture high-strength, high-quality composite materials and articles with thermosetting / thermoplastic polymers.
    As described here, the foam materials of the invention and the corresponding composites are based on cellulose nanomaterials, such as cellulose whiskers (CW), also known as nano crystalline cellulose (NCC), microfibrillary cellulose (MFC), and cellulose bacterial (BC). The processes of the invention require very low energy investment and produce bio-based cellulose nano-foams and composites that exhibit applications both as core materials, as well as insulation materials and structural industrial materials, for example, in the composites and packaging industries .
    Thus, in one aspect of the present invention, a composite article constructed of a structure of cellulose nanomaterial and at least one polymeric resin (of a thermoset polymer or thermoplastic polymer) is provided, the structure of cellulose nanomaterial being of a material selected from cellulose whiskers (CW, also known as nanocrystalline cellulose, NCC), microfibrillar cellulose (MFC) and bacterial cellulose (BC), where at least a polymeric resin at least partially occupying a plurality of pores in the structure.
    As is known in the art, NCC are elongated crystalline nanoparticles in the form of a rod and MFC are elongated ribbons consisting of alternating crystalline and amorphous segments. As used here, MFC also encompasses nanofibrilated cellulose (NFC). Bacterial cellulose (BC) is a nanostructured extracellular product obtained from certain cellulose-producing bacteria such as
    Gluconobacter xilinus. Cellulose fibrils, being generally more crystalline and purer than those obtained from plant sources, are inherently of nano dimensions.
    In some embodiments, cellulose nano-material is characterized by having at least 50% crystallinity. In additional embodiments, the cellulose nanomaterial is mono crystalline.
    In some embodiments, cellulose nanomaterial, produced as particles (for example, fibrils, or in other cases as crystalline material) from cellulose of various origins, as detailed below, is selected to have at least about 100 nm of lenght. In other embodiments, they are at most about 1000 μm in length. In other embodiments, nanoparticles are between about 100 nm and 1000 μm in length, between about 100 nm and 900 μm in length, between about 100 nm and 600 μm in length, or between about 100 nm and 500 μm in length. length.
    In some embodiments, nanoparticles are between about 100 nm and 1000 nm in length, between about 100 nm and 900 nm in length, between about 100 nm and 800 nm in length, between about 100 nm and 600 nm in length , between about 100 nm and 500 nm in length, between about 100 nm and 400 nm in length, between about 100 nm and 300 nm in length, or between about 100 nm and 200 nm in length.
    The thickness of the cellulose nanomaterial can vary between about 5 nm and 50 nm.
    The fibrils of the cellulose nanomaterial can be selected to have an aspect ratio (length-diameter ratio) of 10 and more. In some embodiments, the aspect ratio is 67-100.
    In some embodiments, in which the cellulose nanomaterial is NCC, it is selected to be between about 100 nm and 400 nm in length and between about 5nm and 30 nm in thickness.
    In some embodiments, the composite of the invention comprises at least two types of cellulose nanomaterial.
    As used herein, the term "polymeric resin" refers to a resin of at least one thermoset polymer and / or at least one thermoplastic polymer, which is subjected to curing by heating, a chemical reaction and / or irradiation. The resin can be synthetic, semi-synthetic or a chemically modified natural molecule. The resin can also be obtained from various natural sources, such as natural oils.
    In some embodiments, the polymeric resin is at least a thermoset polymeric resin, being synthetic, semi-synthetic or obtained from a natural source (or as a modified or unmodified resin material). Non-limiting examples of such thermoset resins include: thermoset silicone polymers such as cured silicone elastomers, silicone gels, and silicone resins; and thermoset organic polymers such as furan resins, epoxy resin, amino resins, polyurethanes (polyols and isothiocyanates), polyimides, phenolic resins, cyanate ester resins, bismaleimide resins, polyesters, acrylic resins, and others.
    In some embodiments, the at least one polymer is bio-based. Non-limiting examples of such bio-based resins include: UV-curable epoxylated soybean oil acrylate (UCB, Ebecryl 860), linseed triglycerides and polycarboxylic acid anhydrides (Biocomposites and more, PTP), triglyceride acrylate (Cogins, Tribest S531), epoxylated pine oil residue (Amroy, EPOBIOX ™), DSM Palapreg® ECO P55-01, Ashland Envirez®, unsaturated polyester resins from renewable and recycled sources, soy oil unsaturated polyester (Reichhold, POLILITE 31325-00), liquid epoxy resin based on glycerin (Huntsman) and others.
    In some embodiments, the at least one thermoset resin is a furan resin. In some embodiments, furan resin is selected from liquid furfuryl alcohol resin, furfuryl alcohol formaldehyde resin, furfuryl alcohol furfural formaldehyde resin, phenol furfuryl alcohol resin, furfuryl alcohol urea formaldehyde resin, furfuryl alcohol-urea-phenol and furfural phenol resin.
    In some embodiments, furan resin is furfuryl alcohol resin.
    In some embodiments, the bio-based thermoset furan resin produced from sugarcane bagasse (eg BioRez ™; a two-component resin produced by Transfuran Chemicals bvba, Geel, Belgium).
    According to the present invention, furan can be used in a concentration of about 85% (in water). In some embodiments, the furan resin is diluted with water, or in a water-soluble solvent such as ethanol, to a concentration of 10-65%. In other embodiments, a catalyst is added to the furan resin to catalyze the reaction.
    In other embodiments, the polymeric resin is at least a thermoplastic resin. Non-limiting examples of such thermoplastic resins include: polyolefins, polar thermoplastics, polystyrene, polyvinyl chloride (PVC), acrylonitrile-butadiene-styrene (ABS), styrene copolymers, polyacrylonitrile, polyacrylates, polyacrylamides, vinyl acetate polymers, vinyl acetate polymers vinyl alcohol, cellulose plastics, thermoplastic elastomers, thermoplastic polyurethanes, polyester based thermoplastic elastomers, thermoplastic polyesters, polyethylene terephthalate, polybutylene terephthalate, compatible thermoplastic mixes, polyacetal, polyethers, polyarylates, polycarbonates, polyamides, polyamides, polyamides, polyamides, polyamides, polyamides, polyamides and polyamides polyoxadiazoles, polyphenylquinoxaline, polyphenylene sulphide, polyphenylene vinylene, conductive thermoplastics, conductive thermoplastic composites, poly (aryl ether sulfone) s, poly (aryl ether ketone) s, poly (aryl ether ketones-co-sulfone), poly (aryl ether ether ketone amide) s, polytetrafluoroethylene and mix theirs.
    In other embodiments, at least one resin is selected from a standard polyester, epoxy, and natural rubber.
    In some embodiments, the cellulose nanomaterial is NCC and at least one polymeric resin is furfuryl alcohol resin.
    The composite article of the invention comprises a cellulose nanomaterial, such as NCC, and at least one polymer (originating from the corresponding resin, for example, a furan resin), at a cellulose: polymer weight ratio of about 1: 100 and 100: 1. In some embodiments, the weight ratio is 1:90, or 1:80, or 1:70, or 1:60, or 1:50, or 1:40, or 1:30, or 1:20, or 1:10 cellulose nano-material for polymer. In additional achievements, the ratio is 1:11, 1:12, 1:13, 1:14, 1:15, 1:16, 1:17, 1:18, 1:19, 1:20, 1: 21, 1:22, 1:23, 1:24, 1:25, 1:26, 1:27, 1:28, 1:29, 1:30, 1:31, 1:32, 1:33, 1:34, 1:35, 1:36, 1:37, 1:38, 1:39, 1:40, 1:41, 1:42, 1:43, 1:44, 1:45, 1: 46, 1:47, 1:48, 1:49, 1:50, 1:51, 1:52, 1:53, 1:54, 1:55, 1:56, 1:57, 1:58, 1:59, 1:60, 1:61, 1:62, 1:63, 1:64, 1:65, 1:66, 1:67, 1:68, 1:69, 1:70, 1: 71, 1:72, 1:73, 1:74, 1:75, 1:76, 1:77, 1:78, 1:79, 1:80, 1:81, 1:82, 1:83, 1:84, 1:85, 1:86, 1:87, 1:88, 1:89, 1:90, 1:91, 1:92, 1:93, 1:94, 1:95, 1: 96, 1:97, 1:98, 1:99, or 1: 100. It should be understood that, for example, "a ratio of 1:67" of cellulose nanomaterial to resin is equivalent to a ratio of 2: 134, 4: 268, 30: 2010, etc.
    As stated above, the composite article of the invention is constructed of a structure of a cellulose nanomaterial and at least one polymer, where the polymer forms a material continuity within the structure, i.e., in a plurality of pores in the structure. In some embodiments, the composite material has homogeneous porosity. In order to provide a composite article of the invention with increased mechanical stability, depending on the final intended application, the article can be laminated with a film of a natural or synthetic material. The lamination can be by one or more lamination films positioned on one or more sides of the article. For example, where the article is substantially flat, it can be laminated on both sides with one or more laminating materials. Where the article is constructed as a three-dimensional cube, it can be laminated on all six sides. The laminating film can be selected from natural fabrics, including linen, sisal, wood fibers, and cotton. Other lamination materials can be selected from mineral wool fiber, glass wool, glass fibers, synthetic fibers such as aramid, paper materials, plastic materials and carbon fibers.
    Without attaching to this, laminated articles, that is, laminates produced according to the invention, are suitable for use in internal friezes (for example, in cars, boats, airplanes, etc.), as a fire-resistant material and / or flame retardant article, as insulators for insulation purposes (for example, when rock wool fiber is used), as shock absorbing materials and others.
    In some typical embodiments, the invention provides a laminated composite based on NCC with flat sheets of paper. Generally, such a laminate, as is the case with any other laminate of the invention, can be constructed by connecting at least two flat sheets of the same or a different laminating material, on an external surface (face) of an article. The lamination can be carried out in the presence of pressure and / or heat. In some embodiments, the layers or sheets are composed of a homogeneous mixture of two or more materials. In other embodiments, the materials are not evenly distributed in each of the at least two layers or sheets. In this way, for example, an article of the invention can be laminated on one side with a paper material and on the other side with a natural fabric such as linen. The articles of the invention can be manipulated to a desired shape and size.
    And another of its aspects the present invention provides a process for producing a composite article according to the invention, the process comprising: (a) obtaining a structure of cellulose nano-material (foam, airgel), for example, compound NCC and / or MFC and / or BC; (b) infusing a liquid resin of at least one polymer into the structure in order to obtain continuity of the resin in the structure; (c) curing the product of step (b) to obtain partial or complete curing of the resin.
    In some embodiments, the process further comprising the step of crosslinking the cellulose nanomaterial forming the structure before the resin is infused. In some embodiments, the structure comprises a mixture of NCC and MFC or BC.
    Curing of the resin in the structure can occur at various temperatures between 1 ° C and about 80 ° C. In some embodiments, curing is achieved at room temperature, without the need for external heating. In other embodiments, however, curing is achieved by heating the structure infused with the resin to a temperature above room temperature, for example, to a temperature between about 50 ° C and about 200 ° C. In other embodiments, the curing temperature is between about 70 ° C and about 150 ° C.
    In some embodiments, the resinous material is infused together with at least one accelerator or a catalyst to enable efficient curing, fast curing and / or low temperature curing.
    In other embodiments, the resin contains cellulose nano-material, for example, NCC and / or MFC and / or BC. In other embodiments, the resin is diluted with an organic solvent, such as ethanol or acetone or with water. In some embodiments, the excess resin is drained, for example, by vacuum, or any other method for draining excess liquid, as is obvious to a person skilled in the art, before, during or after partial curing.
    Additional materials can be added to the composite at any stage of the production process. Some non-limiting examples of materials that can be added to the composite material include nanoparticles, which can be added in order to modify the composite's strength, shape and external appearance. The nanoparticles added to the composite material of the invention can, for example, be TiO2 nanoparticles. The addition of TiO2 nanoparticles is of great importance in obtaining, for example, different optical effects on the composite surface. In some embodiments, silver nanoparticles are added to the composite material of the invention, in order to improve the microbial properties of the composite. In other embodiments, nano-clays are added to the composite material in order to mechanically strengthen the composite and provide the composite with strength properties.
    In some additional embodiments, an additional cellulose nanomaterial is added to the composite material, during the preparation of the composite, as needed for the desired application.
    Typically, the curing process does not result in a chemical association (formation of chemical bonds) between the polymeric material and the nano-material composing the structure. Thus, in some embodiments, there is no chemical bond (no chemical bond) between the cured polymer and the structure's nano-material. In additional realizations, where some association exists, the association is a non-covalent bond.
    In some embodiments, the polymeric material and the nanomaterial of the structure are chemically associated by including at least one bonding radical that is capable of binding to both materials or by modifying the nanomaterial and / or the polymeric material of in order to make possible the chemical association between them. Such an association can be selected from covalent bonding, ionic interaction, electronic interaction, complexation (coordinated interaction), hydrogen bonding and so on. In some embodiments, the association is not covalent.
    The cellulose nanomaterial structure, which is employed in a process for the production of a composite material according to the invention, can be produced in a variety of ways, as described here. Once produced, the structure can be strengthened by infusing a polymeric resin, thus resulting in a composite material according to the invention, which is characterized by improved mechanical properties, including high compressive strength and resistance to wet environments.
    As used here, the term "structure" is used interchangeably with "foam" or "airgel" to describe a structure characterized by open cell structures containing pores that are connected together and form an interconnected network. According to the present invention, the structure is produced by trapping water in the pore domains within the solid cellulose nanomaterial and subsequently removing the water using a solvent exchange process by freezing.
    In some embodiments, the foam of cellulose nanomaterial is prepared by: 1. providing a suspension (sludge) of a cellulose nanomaterial in an aqueous medium (water or solvent / solution containing water); 2. freezing of said suspension (to allow the cellulose nano-material to settle); 3. treatment of the frozen suspension under solvent exchange in order to substantially allow the formation of a foam free of water moistened with solvent; and 4. removing the solvent to produce a cellulose foam substantially free of water and solvent.
    In some embodiments, the cellulose nanomaterial is NCC, as defined. The suspension or sludge, for some applications, is a suspension in water, with a concentration of nano-material being below about 50% (w / v). In some embodiments, the concentration is below about 25%. In additional achievements, the concentration is below about 10%. In additional achievements, the concentration is below about 5%.
    In some embodiments, the concentration in the aqueous suspension is at least about 10% (w / v). In additional projects, the concentration is at most about 10%. In additional embodiments, the concentration is between about 10% and about 50%, or between about 10% and 40% or between about 10% and 30%.
    In some embodiments, the concentration in the aqueous suspension is at least about 1% (w / v). In additional projects, the concentration is at most about 10%. In additional embodiments, the concentration is between about 1% and about 10%, or between about 1% and 5% or between about 1% and 2.5%. In additional embodiments, the concentration is below about 2.5% (w / v).
    The freezing step is typically conducted in a mold of a predetermined shape. The mold in which the nano-material suspension is molded can have a shape of any desired architecture. This makes it possible to produce structural parts and core materials of predetermined shapes. Different mold formats and textures are possible, according to the present invention, making it possible to produce parts with various surface textures, such as smooth and nano-patterned surfaces for self-cleaning materials. Some non-limiting examples of mold materials are aluminum, silicone, polystyrene and carbon fiber / epoxy molds.
    Without wishing to be bound by theory, freezing is achieved at any temperature in which cryo-concentration effects occur, where the formation of ice crystals pushes the cellulose nano particles against each other, forcing self-conformation and local disposition of the NCC in macro-structures that are held together by hydrogen bonds. In some embodiments, the temperature at which freezing occurs is below 0 ° C. In other embodiments, said temperature is between about -50 ° C (minus 50 ° C) and about -90 ° C (minus 90 ° C). In additional embodiments, the temperature is between about -60C ° (minus 60C °) and about -80C ° (minus 80C °) and in additional embodiments it is about -70C ° (minus 70C °).
    Next, the frozen foam material is treated to remove substantially all of the water contained therein. This can be achieved first by treating the foam with a water-soluble solvent, for example, ethanol, methanol, acetone, isopropanol, etc., or with an aqueous saline solution (NaCl, NaBr, KCl, KBr and others), under conditions that allow the exchange of the water contained in the cavities of the structure for the solvent soluble in water or with the salt. This can be achieved, for example, by soaking the foam material in a water-soluble solvent bath or in saline. In order to minimize structural damage to the foam, the solvent or saline solution is typically cooled to 4 ° C or less.
    Once the water has been replaced by the water-soluble solvent or saline solution and has been substantially removed from the pore domains of the cellulose nanomaterial foam, the water-soluble solvent or saline solution can be replaced or diluted with a lower water solubility, for example, hexane, t-butanol, or mixtures of these with an alcohol, etc., in order to ensure complete removal of water from said domains and produce a spun material moistened with solvent (saturated with solvent), substantially free of water. The foam can be released from the saturation solvent, for example, by evaporation of the solvent; such evaporation may occur at room temperature or may require vacuum evaporation. The evaporated solvent can be reused. After evaporation of the solvent, water-free foam is obtained which can later be used as described here.
    As stated above, in order to increase or change the mechanical properties of the foam material, the cellulose nano-material used in the preparation of the foam can be cross-linked by means of one or more binding molecules. Cross-linking can be achieved while still in suspension before freezing or in any previous stage or solvent exchange procedure.
    Crosslinking can be obtained as described here. In some embodiments, citric acid is used for the crosslinking of the cellulose nanomaterial (with or without the addition of a catalyst such as TiO2). In other embodiments, 1,2,3,4-butane tetracarboxylic acid (BCTA) is used for the crosslinking of cellulose nano-material.
    Similarly, in some embodiments, the binding molecules are selected from starch, polyethyleneimines (PEI), epoxy-like materials that form ester bonds or ether bonds at alkaline pH and isocyanate / iso-nitrile bi-functional molecules. In other embodiments, crosslinking involves cellulose-modifying proteins (for example, materials containing free amines such as Cellulose Binding Domains (CBD). The foam can be prepared with or without a foaming agent. In some embodiments, the at least one agent foaming is selected from gaseous material such as carbon dioxide, oxygen, nitrogen, and air or a gas-producing material such as sodium bicarbonate, titanium hydride, and others known in the art.
    Alternatively to the above, the composite can be manufactured by direct extrusion of an aqueous suspension of a cellulose nanomaterial, and at least one polymeric resin, with or without a foaming agent, under conditions that allow the cellulose to continue, formation and foam curing. In such embodiments, the conditions may, for example, involve extrusion through a hot spray nozzle at a temperature above 70 ° C, foaming and activating the polymerization of the furan resin. In another aspect of the present invention, a cellulose nanomaterial foam (structure, airgel) having the characteristics mentioned above is provided. In some embodiments, the foam is obtained by a process comprising: 1. preparation of a suspension (sludge) of cellulose nanomaterial in an aqueous medium; 2. freezing said suspension (to produce a frozen aqueous suspension of the cellulose nanomaterial); 3. treatment of the frozen suspension under solvent exchange to produce a foam substantially saturated in a water-free solvent, and 4. removal of the solvent to produce a foam of cellulose nano-material substantially free of solvent and water (characterized by cell structures open pores that are connected to each other and form an interconnected network).
    In some embodiments, the cellulose nanomaterial is NCC, as defined. The suspension or sludge, for some applications, is an aqueous suspension, with the concentration of nanomaterial being below about 50% (w / v). In some embodiments, the concentration is below about 25%. In additional achievements, the concentration is below about 10%. Even in additional projects, the concentration is below about 5%.
    In some embodiments, the concentration in the aqueous suspension is at least about 10% (w / v). In additional projects, the concentration is at most about 10%. In additional embodiments, the concentration is between about 10% and about 50%, or between about 10% and 40% or between about 10% and 30%.
    In some embodiments, the concentration in the aqueous suspension is at least about 1% (w / v). In additional projects, the concentration is at most about 10%. In additional embodiments, the concentration is between about 1% and about 10%, or between about 1% and 5% or between about 1% and 2.5%. In additional embodiments, the concentration is below about 2.5% (w / v).
    The freezing step is typically conducted in a predetermined mold. The mold in which the nano-material suspension is molded can be formatted for any desired architecture. This makes it possible to produce structural parts and core materials of predetermined formats. Different mold shapes and textures are possible according to the present invention, making it possible to produce parts with various surface textures, such as smooth and nano-patterned surfaces for self-cleaning materials. Some non-limiting examples of mold materials are aluminum, silicone, polystyrene and carbon fiber / epoxy composite molds.
    Without wishing to be bound by theory, freezing is achieved at any temperature in which cryo-concentration effects occur, where the formation of ice crystals pushes the cellulose nano particles against each other, forcing a self-arrangement and disposition of the nano- material in macro-structures that are held together by hydrogen bonds. In some embodiments, the temperature at which freezing occurs is below 0 ° C. In other embodiments, said temperature is between about -50 ° C (minus 50 ° C) and about -90 ° C (minus 90 ° C). In additional embodiments, the temperature is between about -60C ° (minus 60C °) and about -80C ° (minus 80C °) and in additional embodiments, the freezing temperature is about -70C ° (minus 70C ° ).
    Next, the frozen foam material is treated to remove substantially all of the water contained therein. This can be achieved by first treating the foam with a water-soluble solvent, for example, ethanol, methanol, acetone, isopropanol, etc., or with an aqueous saline solution, under conditions that allow the exchange of the water contained in the cavities of the structure by water-soluble solvent or salt. This can be achieved, for example, by soaking the foam material in a bath containing the water-soluble solvent or the saline solution. In order to minimize structural damage to the foam, the solvent or saline solution is typically cooled to 4 ° C or less.
    Once water has been replaced by the water-soluble solvent or saline and has been substantially removed from the pore domains of the cellulose nanomaterial foam, the water-soluble solvent or saline solution can be replaced or diluted with a solubility solvent in lower water, for example, hexane, t-butanol, or mixtures of these with an alcohol, etc., in order to ensure the complete removal of water from said domains and to produce a foam material moistened in solvent (saturated in solvent ), substantially free of water. The foam can be dried from the saturation solvent, for example, by evaporation of the solvent; such evaporation may occur at room temperature or may require vacuum evaporation. Evaporated solvents can be reused. After evaporation of the solvent, water-free foam is obtained which can be used as described here.
    In order to increase, or change the mechanical properties of the foam material, the cellulose nano-material used in the preparation of the foam can be cross-linked by means of one or more binding molecules. Cross-linking can be obtained while still in suspension before freezing or at any stage prior to the solvent exchange procedure.
    Crosslinking can be obtained as described here. In some embodiments, citric acid is used for the crosslinking of the cellulose nanomaterial (with or without the addition of a catalyst such as TiO2). In other embodiments, 1,2,3,4-butane tetracarboxylic acid (BCTA) is used for the crosslinking of cellulose nano-material.
    Similarly, in some embodiments, the binding molecules are selected from starch, polyethyleneimines (PEI), epoxy-like materials that form ester or ether bonds at alkaline pH and isocyanate / iso-nitrile bi-functional molecules. In other embodiments, crosslinking involves cellulose-modifying proteins (for example, materials containing free amines such as Cellulose Binding Domains (CBD).
    The foam can be prepared with or without a foaming agent. In some embodiments, the at least one foaming agent is selected from a gaseous material such as carbon dioxide, oxygen, nitrogen and air or a material that produces gas such as sodium bicarbonate, titanium hydride, and others known in the art.
    The inventive cellulose nano-foam (the so-called virgin foam) can serve as a structure into which and / or into which at least one additional component can be introduced in order to impart additional characteristics to the foam material. In some embodiments, the foam of the invention can be infused with a polymeric resin selected from thermoset polymeric resins and natural or synthetic polymeric thermoplastic resins, as defined above. For some applications, the foam of the invention can be manipulated as described above for the production of a composite material according to the invention.
    The cellulose foam nanomaterials of the invention can be coated with a cellulose nanomaterial film by applying a wet suspension of cellulose nanomaterial to the foam walls, followed by immediate drying. This produces a foam reinforcing coating and protects it from external effects such as moisture.
    In order to provide the foam of the invention with increased mechanical stability, depending on the intended final application, the foam can be laminated with a film of a natural or synthetic material. The lamination can be by one or more lamination films positioned on one or more sides of the foam. For example, where the foam is substantially flat, it can be laminated on both sides with one or more laminating materials. Where the foam is constructed as a three-dimensional element, for example, a cube, it can be laminated on all its faces. The laminating film may be of a material selected from fabrics, including linen, sisal, hemp wood fibers, and cotton. Other lamination materials can be selected from mineral wool fiber, glass wool, glass fibers, synthetic fibers such as aramid, paper materials, plastic materials and carbon fibers.
    Without being attached to this, laminated foams are suitable for use in internal moldings (for example, in cars, boats, airplanes, etc.), as a fire resistant material and / or flame retardant composites, as insulators for insulation purposes (for example, when rock wool fiber is used), as shock-absorbing materials and others.
    In some typical embodiments, the invention provides NCC-based foam laminate with sheets of flat paper. Generally, such an NCC-based foam laminate, as is the case with any other laminates of the invention, can be constructed by bonding at least two sheets of the same or different laminating materials on an external surface (face) of the foam. The lamination can be carried out in the presence of pressure and / or heat. In some embodiments, the layers or sheets are composed of a homogeneous mixture of two or more materials. In other embodiments, the materials are distributed inhomogeneously in each of the at least two layers or sheets. In this way, for example, a foam material of the invention can be laminated on one side with a paper material and on the other side with a natural fabric such as linen.
    In this way, the invention provides: 1. Composite articles constructed of a cellulose nanomaterial structure and at least one polymeric resin, the cellulose nanomaterial structure featuring a plurality of open cell structures containing pores that are connected between themselves and form an interconnected network, said pores being at least partially filled with said at least one polymeric resin. 2. Composite articles constructed of a cellulose nanomaterial structure and at least one cured polymer, the cellulose nanomaterial structure featuring a plurality of open cell structures containing pores that are connected together and form an interconnected network, said pores being at least partially filled with said at least one cured polymer. 3. Laminates of composite articles as above. 4. Foam materials of a cellulose nanomaterial having a plurality of open cell structures containing pores that are connected together and form an interconnected network. 5. Laminates of foam materials with the above.
    The products of the invention, including foams, composites and laminates, exhibit physical characteristics that increase the structural and mechanical properties of the articles / devices of which they are part. In this way, the foams and composites of the invention can be used as core materials, acoustic and / or thermal insulation materials, structural support elements, protective layers, elements to increase abrasion resistance, elements to increase shock resistance or impact elements, damping elements, floating devices, filters and others. BRIEF DESCRIPTION OF THE DRAWINGS
    In order to understand the invention and see how it can be carried out in practice, realizations in which at least one cellulose nanomaterial is CW (NCC) will now be described, by way of non-limiting examples only. As a person skilled in the art knows, MFC or BC can be used identically, separately or in combination with NCC. The achievements described here are demonstrated with reference to the accompanying drawings, in which:
    Figs. 1A-1B demonstrate: Fig. 1A clear crystal liquid suspension of 2.5% NCC in water, and Fig. 1B Electron Transmission Microscopy (TEM) image of NCC rods with dimensions 10-20 nm wide, 100-300 nm in length. Figs. 2A-2B demonstrate how self-assembling NCC prepared according to the invention (Fig. 2A foam on the right) differs from a foam not demonstrating self-assembly (Fig. 2A foam on the left). Fig. 2B provides a SEM image of the foam showing its nano-sheet arrangement. Fig. 3 shows a photograph of a virgin solvent-free and water-free NCC foam according to the present invention. Figs. 4A-4C demonstrate the production of NCC foams using paper mill waste as a source of raw material. Fig. 4A - waste from the production of dry tissue paper; Fig. 4B - NCC suspension produced from waste, and Fig. 4C - NCC foam produced from paper mill waste. Figs. 5A-5C show virgin foam compression test curves of NCC (Fig. 5A), NCC reinforced with 50% furan resin (Fig. 5B) diluted in ethanol, and NCC reinforced with 85% (undiluted) resin furan (Fig. 5C). Fig. 6 presents a summary of the results of the compression tests of NCC / furan composite foams reinforced with 50% and 85% furan resin. Fig. 7 shows a ligno-cellulosic composite panel. NCC foam laminated with cardboard used for the production of undulated paper. DETAILED DESCRIPTION OF THE INVENTION
    The NCC foaming mechanism is based on the self-assembly mechanism. The methods for the production of NCC, for example, from MCC, were adopted with some modifications from [8]. The method included the controlled hydrolysis of cellulose fibers with H2SO4 (MCC in this example) followed by washing cycles in water and sonication, resulting in a suspension of cellulose particles similar to optically clear liquid crystalline honey (Fig. 1A). The particle dimensions were measured to be 10-20 nm wide and 100-200 nm long as observed by TEM (Fig. 1B).
    NCC has been shown to form ordered chiral nematic phases shown by birefringence of polarized light, which is typical for cholesteric liquid crystals in similarity to other biomolecules such as chitin, collagen and DNA [1]. The birefringence of typical liquid crital (LC) is demonstrated here when the NCC produced was observed under polarized light microscopy.
    LC suspensions are stable and will not aggregate or flocculate over time. This is explained by the grafting of sulfate groups on the cellulose surface during the acid hydrolysis process. Once the particles are charged with sulfate, they form an electrostatic repulsion that prevents the crystals from forming hydrogen bonds again, for this reason the suspensions are stable "forever". Gelation of suspensions occurs when water-soluble salts or solvents that mask the sulphate repulsion are added to the NCC. In some cases, gelation occurs when NCC suspensions are brought to high concentration (usually above 2.5% to 5%). In both cases, the gelation effect was attributed to the alteration of balance in the direction of formation of hydrogen bonds between the NCC fibers resulting in the formation of a solid 3D network.
    As discussed above, NCC tends to self-assemble on nematic planes. In addition, it has been shown before that the structure is maintained also when water is removed [1], which under normal conditions leads to the formation of a film.
    However, when the suspension is frozen there is the effect of cryo-concentration, where the formation of ice crystals pushes the cellulose nano-particles towards each other, forcing local self-assembly and the disposition of the NCC in macro-structures. nematictics that are held together by hydrogen bonds (similarly to the gelation process in liquid suspensions) while ice prevents the formation of film. In this way, a 3D porous network is formed. In addition, it was discovered that the freezing kinetics was crucial for the formation of ordered nematic planes, as shown by the resistance of the foams and the Scanning Electron Microscopy (SEM) images (Fig. 2A and 2B).
    The nanostructured cellulose foams were produced by others using Cellulose or Microfibrillar or Nanofibrillar, as well as bacterial cellulose (BC). Some have shown the effect of the cooling process on Micro / Nanofibrillar Cellulose (MFC / NFC) foams [9, 10] and their effect on the structure and morphology of the foams. In addition, NCC was applied as a polyurethane foam reinforcement [11]. In comparison with the other cellulosic foams, the NCC foams were unique due to the self-assembly process of the liquid crystals that is described above.
    The direct production of NCC airgel (foam) by gelation of NCC suspension using acetone (without freezing involvement), followed by extraction of supercritical fluid with CO2 resulted in a translucent airgel. However, this method was not feasible for industrial production for several reasons. Extraction of supercritical fluid is a relatively expensive method in cost and the time required from 5 to 7 days for the solvent exchange process is extremely long. In addition, for a production of a volume of 150 ml of airgel, about 850 ml of acetone is required, which is replaced twice a day, for a total of 10 liters of acetone for the entire process [12]. Thus, this process is unlikely to meet the demands of industrial production. It is also expected that the different production method will result in a more random airgel structure, which is expected to be inferior in its mechanical performance. As the process developers indicate, the production process results in random orientation of the NCC crystals. Support for this random arrangement also comes from the high translucency of its aerogels, which attests to the very thin foam walls. Example 1: Production of NCC from micro-crystalline cellulose:
    Suspensions of cellulose nano-whiskers (NCC) were prepared either by acid hydrolysis or by chemical disruption of cellulose fibers. The source of cellulose that was used varied. In all cases, NCC production followed mutatis mutandis the process described below. It should be understood that, although the present example specifically describes the production of NCC from micro-crystalline cellulose, NCC was similarly obtained from other sources such as pulp residue and paper mill. 1. 10 grams of micro-crystalline cellulose with a particle size of 200 μm (MCC, Avicel) were suspended in 200 ml of DDW in a glass vial. 2. The flask was placed in an ice water bath under agitation. 3. H2SO4 was gradually added to a final concentration of 47% while the temperature was kept below 40oC. 4. The suspension was transferred to a water bath at 60oC and incubated under agitation for 30 min, after which it was centrifuged at 8000 rpm for 10 min. 5. The acid was removed and the pellet was resuspended in DDW. The washing and resuspension cycles were repeated 4 to 5 times until the supernatant from the centrifuge was turbid. 6. After the final wash, the NCC was suspended in about 90 ml of DDW (to produce a concentration of about 5% NCC). 7. A sample of the precipitate was weighed before and after drying in order to determine the concentration in whiskers. 8. The suspension was brought to 2.5% and afterwards it was sonicated by a sonicator until the solution became optically clear. The final honey-like viscosity of the liquid crystal suspension was obtained after cooling (cooling takes a few hours). Example 2: Airgel production
    1. A liquid suspension of NCC at a concentration of about 2.5% or less was molded into a mold. 2. The mold containing NCC was directly lyophilized or alternatively frozen at temperatures of -20oC to -178oC (liquid nitrogen) before lyophilization. 3. The NCC was lyophilized for a period of 12 to 24 hours. 4. The resulting product was a highly porous airgel that was released from the mold. Example 3: Production of NCC-furan composites
    1. Liquid furan resin with 1% sulfonide acid catalyst was applied to the NCC foam until the foam was saturated with the resin. 2. The excess furan was drained (for example, under vacuum) and the composite foam was cured at a temperature between 70oC and 150oC until the furan was completely cured. 3. Optionally, the liquid suspension of NCC was mixed in the furan resin before its addition to the NCC foam which allowed a better bonding and and interfaces between the components of the composite. 4. Optionally, sodium bicarbonate was added to the furan to increase the final pore size of the cured airgel. Example 4: Foam production of cellulose nanomaterial of the invention
    A suspension of NCC usually 2.5% in H2O was sonicated with a sonicator for clarification. Immediately after the suspension was molded into a mold. The suspensions were then transferred to a vacuum chamber to remove gas after which it was frozen at -70oC. Subsequently, the "ice cube" formed was transferred to a cold water-soluble solvent, such as acetone and ethanol.
    The foam was kept in the water-soluble solvent, such as ethanol, until it floated, namely, until all the water had been removed and exchanged for ethanol.
    The ethanol was then exchanged with a 70/30 v / v ethanol / hexane mixture or a 70/30 v / v ethanol / tert-butanol mixture. This process was repeated as many times as necessary.
    The resulting foam was of high quality, exhibiting good structural maintenance during the drying process.
    Finally, the solvent-saturated foam was transferred either to a vacuum evaporator or to a chemical evaporator or to a drying oven. The solvents were evaporated to form a dry nano structured airgel (Fig. 3).
    The molds were made of different types of material, for example, aluminum, silicone, polystyrene and carbon fiber / epoxy composite molds were used. In all cases, freezing at a temperature of around -70 ° C led to the required results.
    As stated above, NCC was produced from various sources of raw material such as Micro Crystalline Cellulose (Avicel® PH), bleached softwood pulp, and bleached hardwood pulp, as well as from paper mill sludge. (Figs. 4A-C). In all cases, a successful conversion of NCC suspensions to foam was achieved by employing the same process as the invention. Example 5: Foam reinforcement
    NCC foams that were produced in this way were airgel with a density of 25 kg / m3. Although they are extremely light, they are soft, and can be easily disintegrated. In addition, they exhibit low tensile strengths particularly in wet environments. The foams are strengthened by infusion with polymeric resin resulting in high resistance to compression and resistance to the wet environment.
    The typical resin that was used was a biobased thermoset bio-based thermoset furan resin produced from sugarcane bagasse. BioRez ™, a two-component resin produced by Transfuran Chemicals bvba, Geel, Belgium, was also employed.
    The commercially available furan resin at a concentration of 85% was either used directly or was diluted in water to a concentration between 65% -10%. 1% sulfonic acid was used as a catalyst.
    The resin was infused into the foam followed by vacuum in order to uniformly distribute the resin in the foam and in order to remove excess resin. The foam was cured at 80 ° C for 2 to 12 hrs. The resulting foams were rigid with a compressive strength of up to 10 MPa and a compression module of up to 250 MPa. The density of the foams was 350 to 500 kg / m3 (Figs. 5A-C and 6).
    An additional value of the foams, for example, NCC / furan foams, mechanical resistance, was in terms of their fire resistance properties. When placed in a Bunsen flame, the composite foams self-extinguished when they were removed from the flame and did not burn. Standard polymeric foams are highly flammable and emit toxic gases when they burn. Flame resistant foams exist; they are mainly produced from phenolic foams that are extremely expensive or by the addition of fire retardants (eg, bromide material) to standard polymeric foams.
    The composite foam of NCC / furan has a potential as a low cost flame resistant foam, which makes it possible to use it in applications that are currently banned for standard foams due to the above reasons, such as in the maritime transport market.
    Since the virgin NCC foam serves as a structure, it can be infused with any other natural or synthetic thermo-rigid / permoplastic resins. We have successfully infused other resins such as standard polyester, epoxy, and natural rubber. The polyester and epoxy ones resulted in rigid foams, while the natural rubbers resulted in a flexible foam with high elasticity.
    These examples demonstrate how the NCC foam system is a platform for the production of many potential products. Example 6: Crosslinking
    If cellulose fibers are cross-linked, the technical properties of virgin NCC foam increase to such an extent that it requires little, if any, polymeric resin to obtain the required strength without impairing density. Since the NCC has numerous OH groups on the surface, it can be cross-linked by means of ester bonds and even more preferably the formation of ether bonds.
    The crosslinkers that were chosen are those that were used in the textile industry as a substitute for urea-formaldehyde and in the food and pharmaceutical industries.
    Citric acid containing 3 carboxylic groups with or without the addition of TiO2 was tested as a catalyst. A 2.25% suspension of NCC was mixed with 0.1 M citric acid with or without 0.06% THO2. The suspension was then heated to 80 ° C for 60 minutes resulting in an increase in the viscosity of the suspension indicating crosslinking of the cellulose fibers. The addition of TiO2 appeared to further increase the viscosity. When salt was added to the NCC suspensions, gels were formed. Citric acid does not cause gel formation and the suspension has become viscous as a result of heat treatment. The reaction also took place at room temperature at a lower rate.
    The foams that were produced from these suspensions showed the highest shear strength tested by compression of the foam and a sheet and manual tension at both ends. Non-cross-linked foams were easily broken, while cross-linked foams were difficult to break.
    Another carboxylic acid was 1,2,3,4-butane tetracarboxylic acid (BCTA) which contains 5 carboxylic groups. The catalyst used with BCTA is sodium hypophosphite, NaPO2H2. Example 7: Paper composites
    Composite panels of NCC foam laminated with linerboard paper were produced. The linerboard paper was glued to the NCC with normal “student” paper glue, compressed and cured at 60 ° C overnight. The resulting composite showed high strength and can be suitable for packaging, as well as in construction applications (Fig. 7).
    权利要求:
    Claims (18)
    [0001]
    1. Composite article constructed from a structure of cellulose nano-material and at least one polymeric resin, characterized by the fact that the structure of cellulose nano-material is a material selected from nanocrystalline cellulose (NCC) and microfibrillary cellulose (MFC ), said at least one polymeric resin occupying at least partially a plurality of pores in the structure, and the structure being arranged in nano-sheets.
    [0002]
    2. Article according to claim 1, characterized by the fact that said cellulose nanomaterial is NCC.
    [0003]
    3. Article according to claim 2, characterized in that the NCC is between 100 nm and 400 nm in length and between 5 nm and 30 nm in thickness.
    [0004]
    4. Article according to claim 1, characterized by the fact that the nanomaterial is at least two types of cellulose nanomaterial.
    [0005]
    5. Article according to claim 1, characterized in that the polymeric resin is at least one thermosetting polymer and / or at least one thermoplastic polymer.
    [0006]
    6. Article according to claim 1, characterized by the fact that the polymeric resin is at least a thermoset polymeric resin, being selected from thermoset silicone polymers, silicone gels, and silicone resins; thermoset organic polymers, amino epoxy resin resins, polyurethanes, polyimides, phenolic resins, cyanate ester resins, bismaleimide resins, polyesters, acrylic resins and mixtures thereof, or in which said polymeric resin is at least one thermoplastic resin being selected from polyolefins, polar thermoplastics, polystyrene, polyvinyl chloride (PVC), acrylonitrile-butadiene-styrene (ABS), styrene copolymers, polyacrylonitrile, polyacrylates, polyacrylamides, vinyl acetate polymers, vinyl alcohol polymers, cellulose plastics, cellulose plastics , thermoplastic polyurethanes, polyester-based thermoplastic elastomers, thermoplastic polyesters, polyethylene terephthalate, polybutylene terephthalate, compatible thermoplastic mixtures, polyacetal, polyethers, polyarylates, polycarbonates, polyamides, polyimides, polybenzimidazoles, polyhydrazides, polyhydrazides and polyhydrazides nylene, polyphenylene vinylene, conductive thermoplastics, conductive thermoplastic composites, poly (aryl ether sulfone) s, poly (aryl ether ketones) s, poly (aryl ether ketones-co-sulfones), poly (aryl ether ketone amide) s, polytetrafluoroethylene and mixtures of these.
    [0007]
    7. Article according to claim 5, characterized in that the at least one thermoset resin is a furan resin, optionally selected from liquid furfuryl alcohol resin, furfuryl alcohol-formaldehyde resin, furfuryl alcohol-furfural-formaldehyde resin, furfuryl alcohol resin phenol, furfuryl alcohol urea-formaldehyde resin, furfuryl alcohol urea-phenol resin and furfural phenol resin.
    [0008]
    8. Article according to claim 1, characterized in that the at least one polymeric resin is at least one thermoplastic resin.
    [0009]
    9. Article according to claim 8, characterized in that the thermoplastic resin is selected from polyolefins, polar thermoplastics, polystyrene, polyvinyl chloride (PVC), acrylonitrile-butadiene-styrene (ABS), styrene, polyacrylonitrile, polyacrylates copolymers, polyacrylamides, vinyl acetate polymers, vinyl alcohol polymers, cellulose plastics, thermoplastic elastomers, thermoplastic polyurethanes, polyester-based thermoplastic elastomers, thermoplastic polyesters, polyethylene terephthalate, polybutylene terephthalate, compatible thermoplastic mixtures, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacrylates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates, polyacetates. , polyamides, polyimides, polybenzimidazoles, polyhydrazides and aromatic polyoxadiazoles, polyphenylquinoxalins, polyphenylene sulfide, polyphenylene vinylene, conductive thermoplastics, conductive thermoplastic composites, poly (aryl ether sulfone) s, poly (aryl ether ketone) s, poly (aryl ether ether) s, ketones-co-sulfones), poly ( aryl ether ketone amide) s, polytetrafluoroethylene and mixtures thereof.
    [0010]
    10. Article according to claim 1, characterized in that the cellulose: polymer weight ratio in the article is between 1: 100 and 100: 1.
    [0011]
    11. Article according to claim 1, characterized by the fact that it is in the form of laminate.
    [0012]
    12. Article according to claim 1, manufactured by a process characterized by comprising the steps of: (a) obtaining a cellulose nano-material structure; (b) infusing a liquid resin of at least one polymer into the structure; (c) curing the product of step (b) to achieve partial or complete curing of the resin in the structure.
    [0013]
    13. Article according to claim 12, characterized in that the cellulose nanomaterial structure is prepared by: (a) providing a suspension of a cellulose nanomaterial in an aqueous medium; (b) freezing said suspension; (c) treating the frozen suspension under solvent exchange to produce a wet solvent-free structure, free of water; and (d) removing the solvent to produce a cellulose structure free of solvent and water.
    [0014]
    14. Article according to any one of claims 1 to 13, characterized in that the cellulose nanomaterial is NCC.
    [0015]
    15. Composite article according to claim 1, characterized in that said article is constructed from an NCC structure and at least one polymeric resin, the cellulose nano-material structure has a plurality of open cell structures containing pores which are connected to each other and form an interconnected network, said pores being at least partially filled with said at least one polymeric resin, in which said polymeric resin is optionally cured.
    [0016]
    16. Foam of cellulose nanomaterial, as defined in claim 1, obtained by a process characterized by comprising the steps of: (a) obtaining a suspension of cellulose nanomaterial in an aqueous medium; (b) freezing said suspension to produce a suspension of frozen aqueous cellulose nanomaterial; (c) treating the frozen suspension under solvent exchange to produce a solvent-free, water-saturated foam, and (d) removing the solvent to produce a solvent-free cellulose nano-foam and water.
    [0017]
    17. Foam according to claim 16, characterized in that the cellulose nanomaterial is NCC.
    [0018]
    18. Foam according to claim 16 or 17, characterized in that said foam is infused with a polymeric resin, said foam is coated with a cellulose nano-material film, or said foam is laminated with a film of a natural or synthetic material.
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    同族专利:
    公开号 | 公开日
    CA2810627A1|2012-03-15|
    EP2613935A1|2013-07-17|
    AU2011300350B2|2015-01-15|
    CN103370190A|2013-10-23|
    IL225083A|2017-07-31|
    ES2617986T3|2017-06-20|
    KR20130141475A|2013-12-26|
    JP5930321B2|2016-06-08|
    US9376503B2|2016-06-28|
    JP2013536896A|2013-09-26|
    WO2012032514A1|2012-03-15|
    AU2011300350A1|2013-03-21|
    BR112013005537A2|2018-06-19|
    CN103370190B|2016-05-04|
    EP2613935B1|2016-12-07|
    US20130171439A1|2013-07-04|
    WO2012032514A8|2013-10-10|
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    法律状态:
    2018-06-26| B08F| Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]|
    2018-08-07| B08G| Application fees: restoration [chapter 8.7 patent gazette]|
    2018-08-14| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2019-08-13| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-03-31| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2020-09-24| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2021-02-02| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-04-13| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 07/09/2011, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    US38053810P| true| 2010-09-07|2010-09-07|
    US61/380,538|2010-09-07|
    PCT/IL2011/000714|WO2012032514A1|2010-09-07|2011-09-07|Cellulose-based composite materials|
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