• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    a process for providing water repellent properties to a fibrous material and to the hydrophobic materials and articles thus obtained process for treating a fibrous material, for taking said hydrophobic and / or water-repellent material, which comprises the operation of impregnating said material with a suspension comprising nanoparticles of a hydrophobic material or a cyanoacrylate in an organic solvent to cause cross-linking of said cyanoacrylate; the process uses an amount of cyanoacrylate and a weight ratio with the nanoparticles, in order to produce a complete or partial coating of the fibrous material, with a cross-linked cyanoacrylate matrix where such nanoparticles are dispersed.
    公开号:BR112013015921B1
    申请号:R112013015921-9
    申请日:2011-12-22
    公开日:2020-08-11
    发明作者:Roberto Cingolani；Athanasia Athanasiou；Ilker Bayer
    申请人:Fondazione Istituto Italiano Di Tecnologia；
    IPC主号:
    专利说明:

    [001] The present invention relates to a process for imparting water-resistant, hydrophobic and water-repellent properties to fibrous materials and also to the process for producing fibrous materials from finished articles, having the above mentioned properties together with other properties, such as, in particular, better fireproof properties.
    [002] Recently, there has been considerable interest in processes for the treatment of fibrous materials to obtain functional and environmentally sustainable products.
    [003] In many applications, especially packaging, materials that are hydrophobic and self-cleaning are required. Traditional techniques employed to increase these properties, as well as flame resistance, provide for costly and time-consuming processes for surface modification, for example, the reaction of cellulose with organic components (eg maleic or succinic anhydride) and the application of barrier coatings on the surface, which often involve the use of inorganic substances (for example, metals) and polymerization processes.
    [004] Generally, all of these treatments involve the use of non-biodegradable components, such as metallic or ceramic materials, or require long manufacturing steps that are not suitable for large-scale industrial production.
    [005] In the papermaking industry, the most used technique for the manufacture of hydrophobic paper is the use of alkyl ketene dimers (AKT) in the paper sizing phase.
    [006] The work carried out by Werner et al.in "Cellulose" (2010) 17: 187 - 198, reports the recent developments regarding the techniques for obtaining super hydrophobic paper with the use of ketene dimers and, namely, the techniques of a) crystallization of particles of ketene dimers from organic solvents; b) air jet with cold sprayed cetene dimer particles (cryopowdered) -, and c) spraying using the RESS {Rapid Expansion of Supercritical Solutions} technique.
    [007] GB 2469181 A1 describes the natural cellulose fibers made hydrophobic as a result of the cellulose reaction of the fibers with an aliphatic or aromatic anhydride.
    [008] Biongiovanni et al.in "Cellulose" (DOI 10.1007 / s 10570-010-9451-5, published online on September 18, 2010) describes a process for obtaining sheets of paper made hydrophobic, oleophobic and non-stick by the graft, induced by UV radiation, of fluorinated acrylic monomers on cellulose substrates. The paper sample is immersed in an acetone solution containing fluorinated acrylic monomers and a photoinitiator. After impregnation, the paper is treated with UV radiation and the solvent is extracted in a Soxhlet extractor.
    [009] WO 2007/040493 also describes a process for treating fibrous substrates, in particular paper, to make them hydrophobic with a composition comprising nanocharges of silica or alumina, a photoinitiator comprising an a-hydroxy ketone, at least , a monofunctional acrylate monomer, a diluent for oligomers and a surfactant based on crosslinkable silicone acrylate. The composition is applied to the paper, for example, by spraying or dipping the paper, and the impregnated paper is cured by exposure to heat or actinic radiation.
    [0010] One of the objectives of the present invention is to provide a process for the treatment of fibrous materials that is simple and economical, and makes it possible to obtain fibrous materials that have been made waterproof.
    [0011] A particular objective of the invention is to provide a process that allows to achieve the results described above, using nanocomposites that are biodegradable and biocompatible.
    [0012] Another objective of the invention is to provide a process that makes it possible for the treated material's water resistance to be controlled in a simple way, by regulating, according to the requirements, the concentration of the nanocomposite material applied on the fibrous substrate.
    [0013] Another objective of the invention is to provide a process that makes it possible to obtain, on a fibrous substrate, the insulating characteristics, including, in particular, the hydrophobic properties, those of flame resistance, the fireproof properties, of self- cleaning and water repellency properties, as well as obtaining the reinforcement of mechanical properties for certain substrates, such as, for example, paper.
    [0014] In view of these objectives, the invention refers to a process, as defined in the claims indicated below, the text of which must be considered as an integral part of the technical teaching of the present description.
    [0015] The invention also relates to the fibrous material obtained by the process, according to the invention, as well as to finished articles consisting of or comprising the fibrous material treated by the process of the invention.
    [0016] The process according to the invention is applicable to all fibrous and porous materials, preferably of a hydrophilic nature, whether natural or synthetic, or combinations of natural and synthetic fibers. In particular, the process is applicable to cellulose fibers and cellulose derivatives, for example, cellulose nitrate and cellulose acetate, as well as polyester fibers, including all types of synthetic and natural polyester fibers, including fibers polylactic acid, polyethylene terephthalate or polybutylene terephthalate fibers, for which it is desirable to increase the water repellency characteristics, including combinations of cellulose fibers or cellulose derivatives with polyester fibers.
    [0017] There are no special limitations on the diameter and length of the fibers, in particular, the diameter can vary between 5 pm and 100 pm, preferably between 5 pm and about 20 pm; the length can normally be between 500 pm and 10 cm, in particular between 1000 pm and 5 cm.
    [0018] The fibrous material can be in the form of wicks (roving), felts (felts) or cloths (mats) of cut fibers, non-woven fabric, optionally, needle felt. The process is also applicable to finished articles, such as fabrics, non-woven fabrics, paper, felts, filters and the like.
    [0019] The process according to the invention comprises the following steps: 1. preparation of a suspension comprising hydrophobic nanocharges and at least one cyanoacrylate monomer dispersed in an organic solvent; 2. application of the suspension to the fibrous material and 3. removal of the solvent from the fibrous material, thus treated, and cross-linking ("curing") of the cyanoacrylate monomer.
    [0020] The term "nanoparticles" means that the particles are generally smaller than 1 pm; preferably, particles smaller than 200 nm are used; and the materials used for the nanoparticles are hydrophobic materials, preferably selected from fluorinated polymers, in particular polytetrafluoroethylene, natural and synthetic waxes, for example, carnauba wax, paraffin wax, beeswax, beeswax. polyethylene, polypropylene waxes, Fischer-Tropsch waxes, as well as polymers and copolymers of alpha olefins or cycloolefins (including, in particular, COC) and heavy silicone oils, for example, polydimethylsiloxane polymers; and of course, combinations of nanoparticles of different chemical natures can be used.
    [0021] The cyanoacrylate monomer or monomers preferably comprise alkylcyanoacrylates, where the alkyl group preferably has from 1 to 8 carbon atoms, such as, in particular, methyl-, ethyl-, butyl- and octylcyanoacrylate. These monomers are able to polymerize quickly through nucleophilic polymerization mechanisms, as a result of exposure to even trace amounts of water, and, more specifically, as a result of exposure to hydroxyl ions, which are naturally present on many surfaces as adsorbed ions. The polymerization product maintains the biodegradability characteristics of the monomer.
    [0022] The functions of organic solvents as the suspension vehicle and their selection is not particularly critical. Any organic solvent that allows a stable colloidal dispersion of the hydrophobic material to be obtained can be used. In particular, solvents which have a low boiling point and which are non-aqueous, polar or non-polar, such as acetone, chloroform and mineral oils (Stoddard solvent) are preferred. Hydrocarbon-based solvents are preferred over wax-based nanoparticles.
    [0023] Preferably, the concentration of the cyanoacrylate monomer (or monomers) in the suspension is between 1 and 15% by weight, the concentrations on the order of 3 to 8% by weight, in particular, about 5% by weight is especially preferred.
    [0024] An advantageous feature of the process according to the invention is that the hydrophobicity characteristics obtained in the treated fibrous material can be controlled by adjusting the weight ratio between the cyanoacrylate monomer and the nanocharges. The weight ratios between the cyanoacrylate monomer and the hydrophobic material are 20: 1 and 1: 3, preferably 5: 1 to 2: 1, are generally used.
    [0025] In the case where the waxes are used, they can be previously emulsified in a different solution and then mixed in the cyanoacrylate dispersion in the desired concentration. In this way, the wax particles are encapsulated in the cyanoacrylate polymer resulting from in situ crosslinking, within the fibrous matrix. This is particularly important, as this can avoid washing (ouf) the nanoparticles of the fibrous material, for example, as a result of exposure to high temperatures, increasing the useful life of the final treated fibrous material. The formulation of the suspension does not require the use of surfactants or surface protection agents, however, it is to be understood that the use of said agents is within the scope of the process, according to the invention.
    [0026] The suspensions prepared in this way can be applied to the fibrous material using various conventional techniques, for example, by dipping, spraying, laminating, or by means of solution molding or spray molding techniques.
    [0027] The impregnation is followed by a solvent removal step, which can be carried out at room temperature, by heating, generally, to a temperature not exceeding 80 ° C.
    [0028] The monomer crosslinking, which begins after the solvent evaporation step, is catalyzed by exposure to atmospheric moisture. The crosslinking is thus carried out, preferably at room temperature in the presence of relative humidity above 30%. Temperature and relative humidity conditions of around 60% prove to be ideal for crosslinking and, under these conditions, the crosslinking time is generally 6 to 8 hours. The crosslinking time can, however, be accelerated by heating to elevated temperatures, preferably between 60 ° C and 85 ° C. In addition, crosslinking can be accelerated by immersing the fibrous material in water.
    [0029] The product resulting from the process consists of hydrophobic composite fibers comprising a core of natural or synthetic fiber, provided with a coating or a covering, total or partial, of cyanoacrylate esters, where the nanoparticles are incorporated or encapsulated in the matrix of cross-linked cyanoacrylate.
    [0030] The coating material is hereinafter referred to as biocomposite or nanobiocomposite and can be defined as a semi-interpenetrating system, in which nanoparticles (especially waxes and polytetrafluoroethylene) are efficiently dispersed in a cross-linked cyanoacrylate matrix.
    [0031] A specific application of the process, according to the invention, refers to the impregnation of paper or fabrics or false fabrics.
    [0032] In the attached drawings: - Figure 1 a is a photograph taken with an optical microscope that illustrates the morphology of the untreated fibers and water absorbents for paper; - Figure 1 b is a photograph obtained with an optical microscope of a paper impregnated with bionanocomposite material, where the biopolymer was cross-linked by immersion in water; the areas with dark contrast in the image illustrate the cyanoacrylate polymer globules after rapid cross-linking in water; - Figure 1c is a photograph obtained with an optical microscope, showing the polytetrafluoroethylene particles smaller than pm, connected to the fiber surface by crosslinking the biopolymer, in this case, the biopolymer was made so as to crosslink slowly under environmental conditions; - Figure 2a is a photograph of a pattern printed by laser jet on Xerox water-repellent paper through impregnation with the nanobiocomposite material; the bionanocomposite material is practically invisible and does not affect the laser jet printing process; - Figure 2b is a photograph of paper illustrated in Figure 2a immersed in a water bath at room temperature; the region impregnated with the nanobiocomposite material is visible as a white contrast in the center of the region indicated with the arrows; the untreated regions of the paper begin to disintegrate in water, after immersion, for about 5 minutes; - Figure 2c is a photograph of a paper napkin placed on the paper mentioned above after removing the water bath; the dry region in the center of the napkin corresponds to the paper impregnated with the underlying bionanocomposite material; - Figure 2d is a photograph of the back of the paper, where it can be seen that the treated area is the only area that has remained intact.
    [0033] The following examples illustrate the application of the process to paper and fabrics. Example 1 - Preparation of colloidal dispersions of cyanoacrylate / polytetrafluoroethylene monomer
    [0034] Polytetrafluoroethylene powder was used, with particle size less than 1 pm and, in particular, below 200 nm. The POLITETRAFLUORETHYLENE powder, as received, was lightly added in the form of anhydrous. In a typical procedure, the polytetrafluoroethylene particles were dispersed in chloroform or acetone, and sonicated for 30 minutes at room temperature, without the addition of surfactants or dispersants. After sonication, the polytetrafluoroethylene suspension was stable and there were no large aggregates present in the solution. The ethylcyanoacrylate monomer was added slowly, by dripping, to this solution, until the desired monomer concentration was reached, that is, a concentration of 5% by weight.
    [0035] The suspension was sonicated again for 30 minutes at room temperature; optionally, the final solution can be further diluted with solvents, such as acetone, chloroform and mineral oils (Stoddard solvent), depending on the application and the desired rate of evaporation. The degree of hydrophobicity of the monomer / polytetrafluoroethylene suspension depends on the proportion of monomer / polytetrafluoroethylene in the suspension. For the purpose of making fibrous materials highly water-repellent, it was found that a monomer / polytetrafluoroethylene ratio of 2: 1 was sufficient in dispersions where the total solids content was 10% by weight. Example 2 - Preparation of a colloidal monomer / cyanoacrylate wax dispersion
    [0036] Commercially available paraffin wax or Parafilms (Sigma-Aldrich) were dispersed in chloroform, toluene or Stoddard's solvent. The wax or parafilm does not immediately dissolve in the solvent and complete dissolution was not possible even after one week. In order to disperse the wax or Parafilm completely in the solvents, the solutions were heated to 90 ° C for 15 minutes, stirring continuously from the second day of preparation. After the solutions had cooled to room temperature, the wax or Parafilm dispersed completely in the aforementioned solvents.
    [0037] The ethylcyanoacrylate monomer (ECA) was dispersed separately in each of the aforementioned solvents. The dispersions of wax and ACE were mixed and the mixtures were sonicated for 30 minutes at room temperature. The final mixture was extremely stable and no phase separation was observed after a week of preparing the mixed solutions. The wax and ECA solutions can be mixed in any proportion, which makes it possible to control the hydrophobicity of the resulting composite. A 2: 1 ratio by weight of ACE / wax has proven to be sufficient to make fabrics, particularly those based on cotton, and super hydrophobic (water repellent).
    [0038] It is known that both the composite of ECA / paraffin wax and crosslinked ECA are relatively fragile compared to rubber-based resins. In order to induce greater flexibility, it is possible to use Parafilm, which is a mixture of paraffin wax and polyolefin resin, instead of paraffin wax, depending on the applications or the desired properties. Example 3 - Hydrophobic papermaking
    [0039] Hydrophobic and water-repellent paper was obtained by impregnating Xerox photocopy paper with ECA / wax mixtures as described above. The impregnation was carried out using a dispersion of solids at 5% with a ratio of ECA / wax or Parafilmigual 2: 1. The impregnation was carried out by means of immersion coating techniques, solution molding or spray molding. The solvent was allowed to evaporate at room temperature. After the solvent has evaporated, the ECA begins to crosslink in situ, encapsulating some of the waxes and, at the same time, coating the fibers.
    [0040] In environmental conditions, the cross-linking of the ECA took about 7 hours. At the end of the process, no change in the appearance, thickness and color of the paper can be seen. The contact angles measured in the treated region of the paper were, on average, 110 °, which indicates a good degree of hydrophobicity. The jobs could be printed using laser jet printers, without loss of print quality (see the tests in Figures 2a - 2d). Example 4 - Preparation of super water-repellent paper or fabrics
    [0041] Super hydrophobic papers or super hydrophobic fabrics were obtained by spray coating with a 2: 1 ECA / polytetrafluoroethylene dispersion, with a total solids concentration of 5% by weight.
    [0042] ECA / polytetrafluoroethylene dispersions were also used to spray the coating onto paper and fabrics with a Paasche airbrush. After crosslinking under environmental conditions, the contact angle of the treated paper or fabrics exceeded a value of 160 °. The coated surfaces were extremely stable, even after two weeks of exposure to room temperature. The process was also applied to low density filter papers, for example, lens cleaning papers, which are super hydrophobic.
    [0043] In order to further increase the degree of water repellency, it has also proved possible to apply nanosuspensions in several successive stages, for example, by carrying out a first application stage, by impregnating the paper using immersion in the suspension and, after cross-linking is completed, there is a second stage of application of the nanosuspensions, for example, through spray molding.
    [0044] The invention therefore provides a simple and economical process for the manufacture of commercially available fibrous materials and finished water-repellent articles, avoiding complex methods of producing water-repellent non-woven fabrics or packaging materials.
    [0045] In the process according to the invention, the bionanocomposite coating material is formed within the fibrous matrix, through cross-linking in situ, using atmospheric moisture as a catalyst; therefore, the process does not require expensive technology for thermal crosslinking or crosslinking with ultraviolet radiation.
    [0046] The process can be easily transferred from the laboratory scale to the industrial scale, since the water-repellent nanocomposite material is introduced and impregnated in the fibrous matrix in liquid form.
    [0047] In addition, no pretreatment steps are required for the substrate to which the process is applied, since the process uses a low-viscosity liquid dispersion or suspension as a starting material, it is possible to achieve an effective coating of the fiber surface by simply moistening the fiber surfaces with said dispersion or suspension.
    [0048] Depending on the choice of hydrophobic material, the nanocomposite coating material can be completely biodegradable.
    [0049] Since the nanocomposite coating can be formed by cross-linking catalyzed in situ moisture, nanocomposites have excellent adhesion to fibrous materials, especially cellulose, polyester, cotton, but also to synthetic materials, such as polyamide fibers , which are naturally exposed to humidity in the environment or atmosphere.
    权利要求:
    Claims (14)
    [0001]
    1. Process of treatment of a fibrous material to make the material hydrophobic and / or water-repellent, CHARACTERIZED by the fact that it includes the operation of impregnating said material with a suspension comprising nanoparticles of a hydrophobic material and a cyanoacrylate in an organic solvent in a weight ratio between the cyanoacrylate monomer and the hydrophobic material between 5: 1 and 2: 1 and causing the cyanoacrylate to crosslink, the concentration of the cyanoacrylate in said suspension and its weight ratio to said nanoparticles being such to produce a complete or partial coating of the fibrous material with a cross-linked cyanoacrylate matrix, where said nanoparticles are dispersed.
    [0002]
    2. Process according to claim 1, CHARACTERIZED by the fact that said cyanoacrylate is an alkylcyanoacrylate, where the alkyl has 1 to 8 carbon atoms, or a mixture of said alkylcyanoacrylates.
    [0003]
    3. Process according to claim 1 or 2, CHARACTERIZED by the fact that said hydrophobic material is selected from fluorinated polymers, natural or synthetic waxes, polymers or copolymers of a-olefins or cycloolefins and polymers of polymethylsiloxane.
    [0004]
    4. Process according to any one of claims 1 to 3, CHARACTERIZED by the fact that said hydrophobic material is a wax, selected from carnauba wax, paraffin wax, beeswax, polyethylene waxes, waxes from polypropylene and Fischer-Tropsch waxes.
    [0005]
    Process according to any one of claims 1 to 3, CHARACTERIZED by the fact that said hydrophobic material is polytetrafluoroethylene.
    [0006]
    Process according to any one of claims 1 to 5, CHARACTERIZED by the fact that said fibrous material includes cellulose fibers or fibers derived from cellulose, natural or synthetic polyester fibers and mixtures thereof.
    [0007]
    7. Process according to claim 6, CHARACTERIZED by the fact that said fibrous material comprises fibers selected from cellulose, cellulose nitrate, cellulose acetate, polylactic acid, polyethylene terephthalate, polybutylene terephthalate fibers and mixtures thereof .
    [0008]
    Process according to any one of claims 1 to 7, CHARACTERIZED by the fact that said suspension comprises an alkylcyanoacrylate monomer or a mixture of said monomers, in a concentration of 1% to 15%, by weight, preferably 3% to 8% by weight, based on the weight of the suspension.
    [0009]
    9. Process according to any one of claims 1 to 8, CHARACTERIZED by the fact that said organic solvent is selected from the group consisting of acetone, chloroform and mineral oils.
    [0010]
    10. Process according to any one of claims 1 to 9, CHARACTERIZED by the fact that said suspension is applied to the fibrous material by immersing the material in said suspension, by spraying, by rolling or by molding techniques in solution or molding by spraying.
    [0011]
    11. Process according to any one of claims 1 to 10, CHARACTERIZED by the fact that it includes the operations of removing the solvent from the fibrous material treated with this suspension, by evaporating the solvent, at a temperature not exceeding 85 ° Ç.
    [0012]
    12. Process according to any one of claims 1 to 11, CHARACTERIZED by the fact that the crosslinking of said cyanoacrylate occurs by exposing the fibrous material, treated with such suspension after removal of the solvent, to an environment with a higher relative humidity at 30%, and preferably not less than 60%, optionally with heat treatment at a temperature not exceeding 85 ° C.
    [0013]
    13. Fibrous material CHARACTERIZED by the fact that it comprises natural or synthetic fibers, with a partial or total coating or wrapper, comprising a cross-linked cyanoacrylate matrix, including hydrophobic nanoparticles obtainable by a process, as defined in any of claims 1 to 12 .
    [0014]
    14. Fibrous material according to claim 13, CHARACTERIZED by the fact that said hydrophobic material is selected from the group consisting of polytetrafluoroethylene, natural and synthetic waxes, polymers or copolymers of a-olefins or cycloolefins and polymers polydimethylsiloxane.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3017290A|1957-12-12|1962-01-16|Rohm & Haas|Modified papers and methods for preparing them|
    JP2700149B2|1987-12-30|1998-01-19|株式会社アルファ技研|Waterproof fabric|
    US5653730A|1993-09-28|1997-08-05|Hemodynamics, Inc.|Surface opening adhesive sealer|
    US6495624B1|1997-02-03|2002-12-17|Cytonix Corporation|Hydrophobic coating compositions, articles coated with said compositions, and processes for manufacturing same|
    US20050196431A1|1998-04-30|2005-09-08|Upvan Narang|Adhesive applicator tip with a polymerization initiator, polymerization rate modifier, and/or bioactive material|
    US6183593B1|1999-12-23|2001-02-06|Closure Medical Corporation|1,1-disubstituted ethylene adhesive compositions containing polydimethylsiloxane|
    EP1201220A1|2000-10-27|2002-05-02|L'oreal|Cosmetic or pharmaceutical compositions containing thermostabilising microcapsules|
    US6821631B2|2001-10-29|2004-11-23|Wood Treatment Products, Inc.|Method and composition for treating substrates|
    US20100233146A1|2002-09-09|2010-09-16|Reactive Surfaces, Ltd.|Coatings and Surface Treatments Having Active Enzymes and Peptides|
    JP4635217B2|2003-09-17|2011-02-23|学校法人慶應義塾|Surface treatment agent and material, and surface treatment method|
    CN100359090C|2004-06-11|2008-01-02|财团法人纺织产业综合研究所|Surface treatment method of fabric|
    WO2006002365A2|2004-06-24|2006-01-05|Angiotech International Ag|Microparticles with high loadings of a bioactive agent|
    TWI322208B|2004-07-20|2010-03-21|Schoeller Textil Ag|
    DE102004062742A1|2004-12-27|2006-07-06|Degussa Ag|Textile substrates with self-cleaning properties |
    GB2421727B|2004-12-30|2007-11-14|Ind Tech Res Inst|Method for forming coating material and the material formed thereby|
    CN101137500B|2005-03-09|2011-12-14|美商艾斯登强生股份有限公司|Papermaking fabrics with contaminant resistant nanoparticle coating and method of in situ application|
    CN101171108A|2005-05-02|2008-04-30|巴斯福股份公司|Method for waterproofing lignocellulosic materials|
    US20080247987A1|2005-08-04|2008-10-09|Angiotech International Ag|Block Copolymer Compositions and Uses Thereof|
    JP2009509023A|2005-09-23|2009-03-05|エコロジーコーティングス，インコーポレイテッド|Compositions for impregnating paper products and natural fibers, methods, processes and assembly therefor|
    US20070245500A1|2006-04-13|2007-10-25|Gaelle Brun|Cosmetic composition comprising at least one cyanoacrylate monomer, at least one uncolored heat-stable organic particle and at least one liquid organic solvent and process for using it|
    JP5275583B2|2006-05-30|2013-08-28|株式会社ハイレックスコーポレーション|Medical materials and manufacturing method thereof|
    US20080026662A1|2006-07-25|2008-01-31|Ecology Coatings, Inc.|Flexible Surface Having a UV Curable Waterproofing Composition|
    US8193406B2|2007-05-17|2012-06-05|Ut-Battelle, Llc|Super-hydrophobic bandages and method of making the same|
    US20080286556A1|2007-05-17|2008-11-20|D Urso Brian R|Super-hydrophobic water repellant powder|
    WO2009158046A1|2008-06-27|2009-12-30|The Board Of Trustees Of The University Of Illinois|Polymer composite formulations from poly and cyanoacrylates and methods for use in large-area applications|
    GB2469181A|2009-03-31|2010-10-06|Acetylated Fibres Ltd|Treatment of a natural cellulosic fibre with an anhydride|
    EP2322710B1|2009-11-09|2014-12-17|W.L.Gore & Associates Gmbh|Textile composite article|EP2948299A4|2013-01-25|2016-08-31|Xanofi Inc|Improved hydrophobicity with nanofiber and fluoropolymer coating|
    ITTO20130396A1|2013-05-16|2014-11-17|Fond Istituto Italiano Di Tecnologia|PROCEDURE FOR THE PRODUCTION OF POLICIANO ACRYLATE FIBERS|
    FR3008904B1|2013-07-26|2015-07-31|Inst Polytechnique Grenoble|PROCESS FOR FORMING A HYDROPHOBIC LAYER|
    KR101606770B1|2014-05-12|2016-03-30|사단법인 코티티시험연구원|Water and oil repellent cellulosic textile products and it's manufacturing method|
    EP3362599A4|2015-10-14|2019-05-29|HeiQ Pty Ltd|Process for providing water repellency|
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    KR101912605B1|2017-03-10|2018-10-30|경기대학교 산학협력단|Super-Hydrophobic Particle and Composite having the Same|
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    CN112898629A|2021-02-01|2021-06-04|四川大学|Preparation method of super-hydrophobic full-biomass-based oil-water separation material|
    法律状态:
    2018-06-19| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2019-07-09| B06T| Formal requirements before examination [chapter 6.20 patent gazette]|
    2020-06-16| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2020-08-11| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 22/12/2011, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    ITTO2010A001040|2010-12-22|
    ITTO2010A001040A|IT1403783B1|2010-12-22|2010-12-22|PROCEDURE FOR THE TREATMENT OF FIBROUS MATERIALS TO OBTAIN WATER-REPELLENT PROPERTIES, HYDROPHOBIC FIBROUS MATERIALS AND ITEMS THAT INCLUDE THEM OBTAINED|
    PCT/IB2011/055904|WO2012085879A1|2010-12-22|2011-12-22|A process for providing hydrorepellent properties to a fibrous material and thereby obtained hydrophobic materials|
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