• 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:
    METHOD FOR TREATMENT OF A SURFACE OF A MATERIAL CONTAINING CELLULOSE; AND PRODUCTS RESULTING FROM THE PROCESS. The present invention describes methods of treating cellulosic materials with a composition that provides increased hydrophobicity to these materials without sacrificing their biodegradable character. The methods, as disclosed, provide for the esterification of hydroxyl groups available in cellulosic materials, where those hydroxyl groups are "masked" by bulky organic chains, including the products that the disclosure provides, made by these methods. The materials thus treated exhibit enhanced hydrophobicity, barrier function and mechanical properties, and can be used in any application where these aspects are desired.
    公开号:BR112014032259B1
    申请号:R112014032259-7
    申请日:2013-06-25
    公开日:2021-06-08
    发明作者:Giussepe Trigiante
    申请人:Humanitarian Scientific Llc；
    IPC主号:
    专利说明:

    FIELD OF THE INVENTION
    [001] The present invention relates, in general, to methods of treating materials containing cellulosic compound and, more specifically, to methods to make material based on celluloses more hydrophobic using a composition that esterifies available hydroxyl groups, in which such composition it is useful in surface modification/coating of cellulose based material, including packaging products. HISTORY INFORMATION
    [002] Cellulosic materials have a wide range of applications in industry, such as bulking agents, absorbents, and printing components. Its use is preferred over other material sources because of its high thermal stability, good oxygen barrier function and chemical/mechanical resilience (see, for example, Aulin et al., Cellulose (2010) 17:559-574). It is also of great importance that these materials are completely biodegradable once dispersed in the environment, and that they are totally non-toxic. Cellulose and its derivatives are the material of choice for environmentally friendly solutions in applications such as food product packaging and disposable products.
    [003] The many advantages of cellulose are, however, counteracted by the hydrophobic capacity of the material, which has a high affinity for water and is easily hydrated (see, for example, Aulin et al., Langmuir (2009) 25(13): 7675-7685). While this is a benefit for applications such as absorbents and fabrics, it becomes an issue when secure packaging of aqueous material (eg, food products) is required. Long-term food storage, especially ready-to-use meals that contain a significant amount of water, becomes problematic in cellulose trays as they would first become soggy and then eventually break under. the hydration of your fibers.
    [004] This problem is commonly addressed, in industry, by coating the cellulose fiber with some type of hydrophobic organic material, for example, a resin or a polymer, which would physically protect the water-based hydrophilic cellulose in the contents. Materials such as PVC are routinely used for this purpose and are physically affixed (ie, spray coated) to the surfaces to be treated.
    [005] A similar problem is encountered when sealing food product in its container by means of a film. This film needs even more rigid properties than the container itself. In addition to resistance to mechanical stress, the film must be thin enough to be peelable, ideally transparent, resistant to heat and impermeable to gases such as CO2 and oxygen, non-toxic, and hydrophobic. Again, plastic in the form of polymers and resin is the industry's current solution.
    [006] The need to come up with environmentally friendly as well as renewable packaging solutions has cast a shadow over the use of plastic. New materials have been designed that are derived from natural or semi-synthetic sources and therefore are renewable and/or biodegradable. Materials such as polylactic acid (PLA) and polyhydroxyalkanoate (PHA) are the current gold standards for biodegradable “plastics”. However, they suffer from the disadvantage of heat instability and water sensitivity, which severely limits their use in the packaging industry. It would be desirable to design a coating that is both heat resistant and hydrophobic, without sacrificing the biodegradable characteristic. SUMMARY OF THE INVENTION
    [007] The present disclosure relates to methods of treating cellulosic materials, including treating cellulose-containing materials with a composition that provides increased hydrophobicity, while maintaining the biodegradable characteristic of the cellulosic components. The methods, as disclosed, provide esterification of available hydroxyl groups in cellulose and do not require the use of Lewis acids or separate catalysts to convert said hydroxyl groups to esters, where these hydroxyl groups are "masked" by the bulky organic chains. The coating can be applied to preformed materials.
    [008] In embodiments, a method for treating a surface of a material containing cellulose (or cellulosic) is disclosed, including applying to the surface a composition containing an alkanoic acid derivative having formula (I) or (II ):R-CO-X Formula (I)X-CO-R-CO-X1 Formula (II), where R is a straight-chain, branched-chain or cyclic aliphatic hydrocarbon radical having from 6 to 50 carbon atoms, and wherein X and X1 are independently Cl, Br, or O(CO)OR, wherein, when the alkanoic acid derivative comprises formula (II) X or X1 is the same or different; a base, and a first solvent, heating the surface-applied composition; rinsing the surface with a second solvent; and drying the rinsed surface; wherein the composition esterifies at least a portion of the available hydroxyl groups via the cellulose of the material.
    [009] In one aspect, the material containing cellulose has greater hydrophobicity compared to the material containing cellulose without treatment.
    [010] In one aspect, the base is organic. In a related aspect, the organic base includes aziridines, azetidines, piperazines, piperidines, pyridines, bipyridines, terpyridines, dihydropyridines, morpholines, N-alkylmorpholines, 1,4-diazabicoclo[2.2.2]octanes, 1,8-diazabicycloundecanes, 1 ,8-diazabicycloundecenes, dimethyl pentylamines, trimethyl pentylamines, pyrimidines, pyrroles, pyrrolidines, pyrrolidinones, indoles, indolines, indanones, benzindazoles, imidazoles, benzimidazoles, imidazolones, imidazolines, oxazoles, diaxazoles, isoxazoles, carbazoles, oxazoles, isoxazoles, isoxazoles, , naphthyridines, triazines, triazoles, tetrazoles, triethylamines, pyrazoles, pyrasolines, and combinations thereof.
    [011] In another aspect, the first and second solvents include pentane, hexane, heptane, octane, petroleum ether, naphtha, kerosene, petroleum, paraffin oil, benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, methylene chloride , chloroform, 1,2-dichloroethane, chlorobenzene, carbon tetrachloride, tetrabromoethylene, cyclopentane, cyclohexane, methylcyclohexane, anisole (methyl phenyl ether), methyl tert-butyl ether, dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, triisopropyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether (diglyme), diethylene glycol monobutyl ether, diethylene glycol monomethyl ether, 1,2-dimethoxyethane (DME, monoglyme), ethylene glycol monobutyl ether, triethylene glycol dimethyl ether (triglyme), triethylene glycol monomethyl ether, acetone, diisobutyl ketone, methyl-n-propyl ketone, methyl ethyl ketone, methyl isobutyl ketone, methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, and combinations of these.
    [012] In one aspect, the cellulose-based material comprises a cellulose selected from the group consisting of nanocellulose, cellulose nanofibers, hair crystals or microfibril, microfibrillated cellulose or nanofibril, cotton or cotton blends, sugarcane bagasse cellulose, and combinations of these. In a related aspect, the cellulose-based material includes a food storage box, a shopping bag, eating utensil, container for holding hot or cold beverages, cup, plate, a food storage bag, a bottle for carbonated liquid storage, a non-carbonated liquid storage bottle, food wrapping film, a waste disposal container, a food handling implement, a fabric fiber (eg cotton or cotton blends), an implement of water storage and transportation, a storage and transportation implement for alcoholic or non-alcoholic beverages, an external enclosure or screen for electronic products, an internal or external piece of furniture, a curtain, upholstery, and combinations thereof.
    [013] In the embodiments, a method for treating a surface of a material containing cellulose (or cellulosic) is disclosed, including application to the surface of a composition containing a derivatizing agent that includes acid chloride, acid bromides, iodides of acid, anhydrides, ketenes, diketenes, chlorocarbonic acid esters, carbonic acid diesters, 2,5-diketo-oxazolidines, isatoic anhydride, isocyanates, carbamoyl chlorides, thiocyanates, thiocarbamoyl chlorides, sulfonyl chlorides, anhydrides sulfonic acid, N-chlorosulfonamides, sulfonic acid chloride, N-chlorosulfinamides, and combinations thereof; a base; and a first solvent, heating the surface-applied composition; rinsing the surface with a second solvent; and drying the rinsed surface; wherein the resulting surface of the cellulose-based material has a contact angle with water of about 100°.
    [014] In a related aspect, the composition esterifies at least a portion of the available hydroxyl groups via the cellulose of the material, and the esterified hydroxyl groups are stable to at least about 200°C. In one aspect, the esterified hydroxyl groups they are stable at temperatures between about -100°C to about 250°C. In a further related aspect, the surface of the cellulose-based material has a contact angle with water between about 60° to about 120° . In another related aspect, the surface treatment is chemically stable at temperatures between about 200°C to about 250°C. In one aspect, the esterified hydroxyl groups are stable at temperatures between about -100°C to about 250°C. In another related aspect, the water vapor permeability of the treated surface is between about 10 Barrer units to about of 20 Barrer units. In a further aspect, the oxygen permeability of the treated surface is between about 10 Barrer units to about 20 Barrer units. In another related aspect, the portion of the hydroxyl groups available on the cellulose surface that are esterified by the composition is between about 35 to about 40%, about 40% to about 50%, about 50% to about 60% , about 60 to about 70%, about 70% to about 80%, about 80% to about 90%, and about 90% to about 100%. In embodiments, the share of available hydroxyl groups is about 70%.
    [015] In the embodiments, the compositions esterify at least a part of the hydroxyl groups available through the cellulose of the material with the dicarboxylic acid derivative (see, for example, binder of Formula (I)) to increase mechanical and thermal stability. In one aspect, the esterified hydroxyl groups are stable at temperatures between about -100°C to about 300°C. In a related further aspect, the surface of the cellulose-based material has a contact angle with water between about from 60° to about 120°. In another related aspect, the surface treatment is chemically stable at temperatures between about 200°C to about 300°C.
    [016] In a related aspect, the composition crosslinks adjacent cellulose chains by esterification with both ends of a dicarboxylic acid derivative (Formula (II)) to enhance both mechanical and thermal stability. In one aspect, the esterified hydroxyl groups are stable at temperatures between about -100°C to about 300°C. In a further related aspect, the surface of the cellulose-based material has a contact angle with water between about and about from 60° to about 120°. In another related aspect, the surface treatment is chemically stable at temperatures between about 200°C to about 300°C.
    [017] In the realizations, the composition applied to the material based on cellulose (or cellulosic) is a biodegradable product. In a related aspect, the product includes a food storage box, a shopping bag, eating utensil, container for holding hot or cold beverages, cup, plate, a food storage bag, a carbonated liquid storage bottle. , a non-carbonated liquid storage bottle, food wrapping film, a garbage disposal container, a food handling implement, a fabric fiber, a water storage and transport implement, an alcoholic beverage storage and transport implement or non-alcoholic, an outdoor housing or screen for electronics, an indoor or outdoor piece of furniture, a curtain, and upholstery.
    [018] In the embodiments, a method for treating a surface of a material containing cellulose (or cellulosic) is disclosed, including application to the surface of a composition containing an alkanoic acid derivative having the formula (I) or (II): R-CO-X Formula (I)X-CO-R-CO-X1 Formula (II), where R is a straight-chain, branched-chain or cyclic aliphatic hydrocarbon radical having from 6 to 50 carbon atoms, and in that X and X1 are independently Cl, Br, or O(CO)OR; a base; and a first solvent, heating the composition applied to said surface; rinsing the surface with a second solvent; and drying the rinsed surface; wherein the resulting treated material containing cellulose has properties including a water contact angle of about 100°, is stable up to at least about 200°C, an oxygen permeability of less than about 10 Barrer units, a water vapor permeability of less than about 20 Barrer units, and combinations thereof. BRIEF DESCRIPTION OF THE DRAWINGS
    [019] Figure 1 shows an illustration of the surface of a cellulosic material before and after treatment, as revealed. DETAILED DESCRIPTION OF THE INVENTION
    [020] Before the present composition, methods, and methodologies are described, it is to be understood that this invention is not limited to the particular compositions, methods, and experimental conditions described, since compositions, methods, and conditions may vary. It is also to be understood that the terminology used herein is for the purpose of describing the particular embodiments only, and is not intended to be limiting, as the scope of the present invention will be limited only by the appended claims.
    [021] As used in this specification and the appended claims, the singular forms "a", "an", and "the" include plural references unless the context clearly indicates otherwise. Thus, for example, references to "a derivation agent" include one or more derivation agents and/or compositions of the type described herein that will become more apparent to those skilled in the art upon reading this disclosure, and so forth.
    [022] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Any methods and materials similar or equivalent to those described herein may be used in the practice or testing of the invention, as it will be understood that modifications and variations are encompassed within the spirit and scope of the subject disclosure.
    [023] It is well known that esters are organic molecules with a high biodegradable characteristic, since bacterial enzymes readily break them down. However, they are relatively stable to chemical agents such as heat.
    [024] In the embodiments, the present disclosure presents that, by treating the surface of cellulose fibers with long-chain alkanoic acid derivatives, the resulting surface becomes strongly hydrophobic, since the cellulosic hydroxyl groups are masked by bulky organic chains (See, for example, FIGURE 1). Furthermore, if the alkanoic acid chain is bifunctional having two carboxyl groups at both ends, the resulting diester can function as a crosslink between isolated cellulosic fibers and increases the thermal and mechanical strength of the cellulosic fiber itself. These organic chains, once removed by bacterial enzymes, are easily digested as such. The derived surface exhibits a great deal of heat resistance, being able to withstand temperatures as high as 250°C and is obviously more impermeable to gases than the filmless underside. The material is also transparent and resistant to mechanical damage as it binds by covalent bonding. In the realizations, the material is semi-transparent, non-transparent and of different colors. The material is therefore an ideal solution to the problem of hydrophilic cellulose surface derivation, in any embodiment in which cellulose materials can be employed.
    [025] As used herein, "cellulosic" means natural, synthetic or semi-synthetic materials that can be molded or extruded into objects or films or filaments, which can be used to make such objects or films or filaments, which are structurally or functionally similar to cellulose, eg coatings and adhesives (eg carboxymethyl cellulose). In another example, cellulose, a complex carbohydrate (C6H10O5)n that is composed of the glucose unit, which forms the main constituent of the cell wall in most plants, is cellulosic.
    [026] As used herein, "hydrophobicity" means the property of repelling water, tending to repel and not absorb water.
    [027] As used herein, "cellulose-containing material" or "cellulose-based material" means a composition consisting essentially of cellulose. For example, such material may include, but are not limited to, a food storage box, a food storage bag, a shopping bag, an eating utensil, a container for holding hot or cold beverages, a cup, a plate, a storage bottle. of carbonated liquid, a bottle for storing non-carbonated liquid, food wrapping film, a waste disposal container, a food handling implement, a fabric fiber (eg, cotton or cotton blends), an implement. storage and transportation of water, alcoholic or non-alcoholic beverages, an external enclosure or screen for electronic products, an internal or external piece of furniture, a curtain and upholstery.
    [028] As used herein, “water contact angle” means the angle measured through a liquid, at which a liquid/vapour interface meets a solid surface. The wettability of the solid surface by the liquid is quantified. The contact angle is a reflection of how strongly liquid and solid molecules interact with each other, relative to how strongly each interacts with its own type. On many highly hydrophilic surfaces, water droplets will have contact angles of 0° to 30°. In general, if the contact angle with water is greater than 90°, the solid surface is considered hydrophobic.
    [029] As used herein, "water vapor permeability" means breathability or a textile ability to transfer moisture. There are at least two different measurement methods. One, the MVTR (Moisture Vapor Transmission Rate) test, according to ISO 15496, describes the water vapor permeability (WVP) of a fabric and therefore the degree of transport of perspiration to the outside air. Measurements determine how many grams of moisture (water vapor) pass through a square meter of fabric in 24 hours (the higher the level, the greater the breathability).
    [030] As used herein, "oxygen permeability" means the degree to which a polymer allows the passage of a gas or fluid. Oxygen permeability (Dk) of a material is a function of the diffusivity (D) (ie, the rate at which oxygen molecules pass through the material) and the solubility (k) (or the amount of oxygen molecules absorbed, per volume, in the material). Oxygen permeability (Dk) values typically fall within the range 10-150 x 10-11 (cm2 ml O2)/(s ml mmHg). A semi-logarithmic relationship was demonstrated between hydrogel water content and oxygen permeability (Unit: Barrer unit). The International Organization for Standardization (ISO) specified permeability using the hectopascal (hPa) SI unit for pressure. Hence, Dk = 10-11 (cm2 ml O2)/(s ml hPa). The Barrer unit can be converted to the hPa unit by multiplying it by the constant 0.75.
    [031] As used herein, “biodegradable,” including its grammatical variations, means capable of being broken down especially into innocuous products by the action of living things (eg, by microorganisms).
    [032] As used herein, "pure" means that there is substantially no other molecule present in the substance, including the absence of a solvent.
    [033] The process, as disclosed, includes a one-step reaction involving a solvent (eg toluene), an alkanoic acid derivative (eg acid halide) and a base such as pyridine to be placed in a surface containing cellulosic and heated, in the embodiments, for a period of minutes to hours (it should be readily apparent to one skilled in the art that the period of time and temperature used in the reaction may vary depending on the reactants and may be adjusted accordingly). In embodiments, any resulting gases are vented. The process, as disclosed, ensures that the hydroxyl groups on the surface are permanently affixed (covalently bonded) to the alkyl groups and can only be degraded by bacterial enzymatic intervention or very hard acid or extreme bases.
    [034] The acid derivatives suitable for the practice of the present invention are those having the general formula: R-CO-X Formula (I) or X-CO-R-CO-X1 Formula (II), wherein CO is the group carbonyl C=O, R is selected from straight-chain, branched-chain or cyclic aliphatic hydrocarbon radicals having from about 6 to 50 carbon atoms and X and X1 independently represent the specific acid derivative substituent such as Cl, Br or O(CO)OU, in the case of anhydrides. In one aspect, X and X1 can be the same or different.
    [035] In the embodiments, the ligands themselves can be attached in structures such as: where CO is the carbonyl group C=O, R is selected from straight chain, branched chain or cyclic aliphatic hydrocarbon radicals having from about 6 to 50 carbon atoms and X1 and X2 represent the substituent of a specific acid derivative such as Cl, Br or O(CO)OR in the case of anhydrides. In one aspect, X1 and X2 can be the same or different, wherein MFC is microfibrillated cellulose.
    [036] In other respects, other binders may include:
    where CO is the carbonyl group C=O, R is selected from straight-chain, branched-chain or cyclic aliphatic hydrocarbon radicals having from about 6 to 50 carbon atoms, and X, X1, X3, and X4 independently represent the specific acid derivative substituent such as Cl, Br or O(CO)OR in the case of anhydrides. In one aspect, X, X1, X3, and X4 can be the same or different.
    [037] In a related aspect, X3 and X4 represent derivatives that may allow cross-linking to others after the MFC has been modified by X and X1.
    [038] In the embodiments, the crosslinkers can be used to conjugate a mixture of different celluloses, including the introduction of binders that can allow the crosslinking of said difference of celluloses. In one aspect, the resulting mixture can provide more favorable physical or chemical properties to the surface. In another aspect, binders may include:
    wherein CO is the carbonyl group C=O, R1 and R2 are independently selected from straight-chain, branched-chain or cyclic aliphatic hydrocarbon radicals having from about 6 to 50 carbon atoms, and X1 and X2 independently represent the substituent of derived from a specific acid, such as Cl, Br or O(CO)OR, in the case of anhydrides. In one aspect, R1 and R2 can be the same or different. In another aspect, R1 and R2 can be the same or different, wherein R2 comprises reactive groups that allow cross-linking to other groups R2, R1 or to cellulose. In a related aspect, X1, and X2 can be the same or different.
    [039] In one aspect, the cellulose material is pretreated to add additional OH groups to the cellulose surface, which, in turn, are esterified by the alkanoic acid derivatives to increase mechanical and thermal stability as well as increase potency. tensile.
    [040] In the embodiments, the compositions esterify at least a part of the hydroxyl groups available through the cellulose of the material with the dicarboxylic acid derivative (see, for example, binder of Formula (I)) to increase both mechanical and thermal stability . In one aspect, the esterified hydroxyl groups are stable at temperatures between about -100°C to about 300°C. In a related further aspect, the surface of the cellulose-based material has a contact angle with water between about from 60° to about 120°. In another related aspect, the surface treatment is chemically stable at temperatures between about 200°C to about 300°C.
    [041] In the embodiments, the above compositions cross-link adjacent cellulose chains by esterification with both ends of a dicarboxylic acid derivative (see, for example, binder of Formula (II)) to increase both mechanical and thermal stability. In one aspect, the esterified hydroxyl groups are stable at temperatures between about -100°C to about 300°C. In a related further aspect, the surface of the cellulose-based material has a contact angle with water between about from 60° to about 120°. In another related aspect, the surface treatment is chemically stable at temperatures between about 200°C to about 300°C.
    [042] In the embodiments, the method, as disclosed, can be used on any surface based on cellulose, including, but not limited to, a film, a rigid container, a fabric or the like. In addition, the method may include the use of carboxylic acid halide or the like (eg, anhydride, ketenes and the like), a suitable non-nucleophilic, non-protic solvent, in which the reaction may proceed (eg, toluene, xylene, dioxane, aliphatic and aromatic esters and esters) and a non-nucleophilic base to neutralize any acidity involved (eg, among others, pyridine). In embodiments, the solvent can be placed between about 100°C to about 120°C under agitation. The non-nucleophilic base, which may be present at between about 5% to about 10% of the reaction volume, can be added to the acid halide, which acid halide may be present at between about 5% to about 10%, therewith the combined materials (ie modification mixture) above are ready to be applied to a cellulose-containing surface (ie the substrate). The substrate that can be dried before application (eg at about 100°C), can be treated with the modification mixture by dipping, for example, and allow the surface to be exposed to the mixture for about 2 minutes at about 5 minutes. The surface can then be removed from the mixture and rinsed with water or a hydro-polar organic solvent solution (eg 70% EtOH) to remove traces of reagents, such solutions will be apparent to the skilled person. The substrate can be air-dried or heated to dry the surface, after which the modified material is ready for use.
    [043] In general, it has been found that acyl groups containing less than about 6 carbon atoms in chain length do not produce satisfactory water repellency. Likewise, chain lengths greater than 6 carbon atoms can be used to practice the invention as disclosed. In embodiments, chain lengths can be 8-50, 10-40, and 10-30 carbon atoms. In embodiments, the carbon atom chain length can be 10-20 carbon atoms. Examples of compounds where R (including R1 and/or R2) is selected from aliphatic hydrocarbon radicals are caprylic chloride, decanoyl chloride, lauroyl chloride, palmitoyl chloride and myristoyl chloride. Examples of compounds of R selected from cyclic aliphatic hydrocarbon radicals are cyclohexanecarboxylic acid halide. However, generally speaking, straight-chain aliphatic acid halides or anhydrides can be used for this process, as they are commonly cheaper and more readily available, and also because branched-chain and cyclic hydrocarbon radicals are not. Easily biodegradable. In some embodiments, it may be desirable to employ a mixture of two or more acid anhydrides, and such embodiments are within the scope of the present disclosure. Also, acid bromides and acid iodides react in similar ways to acid chloride and can be substituted for this. However, because bromides and iodides are generally more expensive and less readily available, the equivalent acid chloride can be used. For the practice of the present methods, it has been found that common commercial grade acid chloride is completely adequate, the only precaution necessary being to prevent exposure of the easily hydrolysable acid anhydrides to moisture.
    [044] In embodiments, acid derivatives (or derivatizing agents) include acid chloride, acid bromides, acid iodides, anhydrides, ketenes, diketenes, chlorocarbonic acid esters, carbonic acid diesters, 2,5- diketooxazolidines, isatoic anhydride, isocyanates, carbamoyl chlorides, thiocyanates, thiocarbamoyl chlorides, sulfonyl chlorides, sulfonic acid anhydrides, N-chlorosulfonamides, sulfinic acid chloride, N-chlorosulfinamides, and combinations thereof. In embodiments, the amount of acid derivative (or derivatizing agent) present in the coating mixture is about 0.1M to about 1M, about 1M to about 2M, in embodiments about 2M to about 3M, in the realizations about 0.1M to about 3M.
    [045] Although not wishing to be bound by theory, the thickness of the coating, as revealed, is independent of the amount of reagent and, in contrast, it relies on the length of the alkyl chain R, since there is no physical absorption of the coating in the substrate, but a chemical bonding reaction, which can be variable, in the surface hydroxyl layer. Furthermore, this reaction (ie, esterification) may not be reiterated as the hydroxyl groups react with the acid derivative.
    [046] No special preparation of the material is required in the practice of this invention, including that no separate Lewis acids or catalysts are required, except that the surface to be treated must be clean and free from dirt and excess moisture. In embodiments, air-dried material normally that contains a small percentage of absorbed moisture can be used. In some embodiments, material can be dried prior to treatment (eg, at about 100°C to about 110°C, for a few minutes) to remove most of the absorbed moisture. The degree of water tightness can be controlled by selecting the thickness of the cellulose to be treated and also by varying the treatment conditions, in particular the acid derivative selected, the acid derivative concentration in the reaction chamber and the duration of exposure.
    [047] Depending on the origin, cellulose can be nanocellulose, cellulose nanofibers, hair crystals or microfibril, microfibrillated, cotton or cotton blends, or nanofibrillated cellulose.
    [048] In embodiments, the amount of coating applied is sufficient to completely cover at least one surface of a cellulose-containing material. For example, in the embodiments, the coating can be applied to the complete outer surface of a container, the complete inner surface of a container, or a combination thereof. In other embodiments, the complete upper surface of a film may be covered by the coating, or the complete lower surface of a film may be covered by the coating, or a combination thereof. In some embodiments, the lumen of a device/instrument may be covered by the coating or the outer surface of the device/instrument may be covered by the coating, or a combination thereof. In the embodiment, the amount of coating applied is sufficient to partially cover at least one surface of a cellulose-containing material. For example, only surfaces exposed to the ambient atmosphere are covered by the coating or only surfaces that are not exposed to the ambient atmosphere are covered by the coating. As will be apparent to one skilled in the art, the amount of coating applied will depend on the use of the material to be coated.
    [049] Any suitable coating process can be used to release any of the various coatings applied in the evolving practice of this aspect of the method. In the embodiments, coating processes include dipping, spraying, painting and any combination of these processes, alone or with other coating processes adapted to practice the methods as disclosed.
    [050] In general, longer chain acid derivatives give greater impermeability, other factors such as depth of treated cellulose being equal. By increasing the acid derivative concentration, for example, to about one molar or increasing the exposure time, an acid derivative can react more extensively with the cellulose being treated with the net result, again, in which these characteristics improved water repellents are featured.
    [051] The invention correspondingly provides a method to achieve such a coating by dissolving the modifying agent in a suitable solvent, such as a C4-C8 ether, ester, ketones, starches or nitriles, or aromatic compound, such as xylene or toluene, together with a non-nucleophilic base such as pyridine, to absorb the acid generated. The mixture is sprayed onto the material to be derived and heated at about 100°C to about 115°C, 120°C to about 210°C or about 120°C to about 150°C for a variable period ( for example, for about 10 minutes to about 30 minutes, about 30 minutes to about an hour, about 1 hour to about 1.5 hours, about 2 to about 2.5 hours, about 2.5 hours to about 3 hours or from about 2 hours to about 3 hours). The surface can then be rinsed with detergent (surfactant) and water or a solvent (eg acetone), or a mixture of these, and dried again. A surfactant can be an ionic surfactant (cationic and anionic), a non-ionic surfactant, or a combination of these.
    [052] Any suitable basic neutralizing reagent can be used, in accordance with the present disclosure, as long as the base is non-nucleophilic so as not to react with the acid derivative. In embodiments, suitable basic neutralizing agents can include basic organic agents. Suitable basic agents can include monocyclic compounds and polycyclic compounds having at least one nitrogen nitro such as, for example, secondary amines, which include aziridines, azetidines, piperazines, piperidines, pyridines, bipyridines, terpyridines, dihydropyridines, morpholines, N-alkylmorpholines, 1,4-diazabicoclo[2.2.2]octanes, 1,8-diazabicycloundecanes, 1,8-diazabicycloundecenes, dimethyl pentylamines, trimethyl pentylamines, pyrimidines, pyrroles, pyrrolidines, pyrrolidinones, indoles, indolines, indanones, benzindazoles, imidazoles, imidazoles imidazolones, imidazolines, oxazoles, isoxazoles, oxazolines, oxadiazoles, thiadiazoles, carbazoles, quinolines, isoquinolines, naphthyridines, triazines, triazoles, tetrazoles, triethylamine, pyrazoles, pyrasolines, and combinations thereof. In embodiments, monocyclic and polycyclic compounds can be unsubstituted or substituted at any carbon position in the ring. In embodiments, the amount of base present in the coating mixture can be from about 0.1M to about 1M, about 1M to about 2M, about 2M to about 4M, about 0.1M to about 3M , or about 0.1M to about 5M.
    [053] Suitable solvents include non-nucleophilic aliphatic hydrocarbons such as pentane, hexane, heptane, octane, and petroleum ether, naphtha, kerosene, petroleum, paraffin oil, etc.; aromatic hydrocarbons such as benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, etc.; halogenated hydrocarbons such as methylene chloride, chloroform, 1,2-dichloroethane, chlorobenzene, carbon tetrachloride, tetrabromoethylene, etc.; alicyclic hydrocarbons such as cyclopentane, cyclohexane, e, methylcyclohexane etc.; ethers such as anisole (methyl phenyl ether), methyl tert-butyl ether, dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, triisopropyl ether etc.; ether glycols such as diethylene glycol diethyl ether, diethylene glycol dimethyl ether (diglyme), diethylene glycol monobutyl ether, diethylene glycol monomethyl ether, 1,2-dimethoxyethane (DME, monoglyme), ethylene glycol monobutyl ether, triethylene glycol dimethyl ether (triglyme), triethylene glycol monomethyl ether etc. ; ketones such as acetone, diisobutyl ketone, methyl-n-propyl ketone; methyl ethyl ketone, methyl isobutyl ketone etc.; esters such as methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, and n-butyl acetate, etc.; carboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid etc. One or more of these compounds can be used, alone or in combination. In embodiments, the amount of solvent present can be about 50% to about 99%, about 60% to about 95%, about 75% to about 90% (% by vol.).
    [054] It will be apparent to a person skilled in the art that the selection of cellulose to be treated, the acid derivative reagent, the reaction temperature (or vapor pressure) and the exposure time are process parameters that can be optimized by routine experimentation to tailor any particular application to the final product.
    [055] In the embodiments, among useful coating agents, these agents may include, among others, acid halide, acid anhydrides, esters, ketenes, diketenes, chlorocarbonic acid esters, carbonic acid diesters, 2,5- diketooxazolidines, isatoic anhydride, isocyanates, carbamoyl chlorides, thiocyanates, thiocarbamoyl chlorides, sulfonyl chlorides, sulfonic acid anhydrides, N-chlorosulfonamides, sulfinic acid chloride, N-chlorosulfinamides.
    [056] Derived materials have altered physical properties that can be defined and measured using suitable tests known in the art. For hydrophobicity the analytical protocol is the measurement of the contact angle, in which a drop of water is deposited on the surface and the interface angle measured using one of the many commercial instruments available for the purpose. A specific standardized protocol below is defined by the American Society for Testing and Materials (ASTM protocol D7334 - 08).
    [057] The permeability of a surface to various gases, such as water vapor and oxygen, can also be changed by the coating process as the material's barrier function is improved. The standard unit that measures permeability is Barrer and protocols for measuring these parameters are also available in the public domain (ASTM std F2476-05 for water vapor and ASTM std F2622-8 for oxygen).
    [058] In the embodiments, materials treated according to the currently disclosed procedure exhibits a complete biodegradable characteristic, as measured by degradation in the environment, under attack by microorganisms.
    [059] Several methods are available to define and test biodegradable characteristics including the shake flask method (ASTM E1279 - 89(2008)) and the Zahn-Wellens test (OECD TG 302 B).
    [060] In the embodiments, the derived surface can be characterized for several parameters pertinent to the newly formed water barrier function, as set out below: 1) Degree of substitution. By comparing the dry weight of the derived item and the dry weight of the untreated substrate, the degree of substitution of the hydroxyl groups on the surface can be determined using the equation: %S = (W2-W1)/(MW - 1 - MWx)/ DOH * 100, where W2 and W1 are the weight area per unit after and before treatment, respectively, MW is the molecular weight of the derivation agent, MWx is the weight of the portion affixed to the C=O group in the molecule and DOH is the density of hydroxyl groups on the cellulose surface. Typical results obtained by the methods described here are in the range of about 60% to about 80% replacement, with a minimum requirement of about 50%. 2) Contact angle. The contact angle between a drop of water and the surface is an indicator of the hydrophobicity of the surface itself. This can be measured by standard techniques as mentioned above. Typical results obtained by the methods as described herein are about 90°, with variations from about 70° to about 110°. 3) Water vapor transmission rate (see above), which can be used to determine the water barrier function. Derivation leads to an improvement of this parameter by at least two times compared to an underived surface. Typical results obtained by the method, as described here, are 670 g/m2 24h (compared to >1200 g/m2 24h for untreated surfaces).4) Heat stability of the barrier function. The barrier function is retained at temperatures up to about 200°C using the methods as described herein. This can be determined by heating triglycerides in a coated tray to said temperature and checking the amount of absorption of triglycerides in the tray itself.
    [061] Materials suitable for treatment by the process of this invention include various forms of cellulose, such as cotton fibers, vegetable fibers such as linen, wood fibers, regenerated cellulose (rayon and cellophane), partially alkylated cellulose (cellulose ethers), cellulose partially esterified (acetate rayon), and other modified cellulose materials that have a substantial portion of their hydroxyl groups available for reaction. As stated above, the term "cellulose" includes all such materials and others of similar polysaccharide structure and having similar properties. Among these, microfibrillated cellulose of relatively innovative material (nanocellulose) (as defined, for example, in U.S. Patent US4374702 and application 20090221812, incorporated herein by reference in their integrity) is particularly suitable for this application, as it can form transparent films with high specific strength. In other embodiments, celluloses may include, but are not limited to, cellulose triacetate, cellulose propionate, cellulose acetate propionate, cellulose acetate butyrate, nitrocellulose (cellulose nitrate), cellulose sulfate, celluloid, methylcellulose, ethylcellulose, ethyl methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl methyl cellulose, hydroxypropyl methyl cellulose, ethyl hydroxyethyl cellulose, carboxymethyl cellulose, and combinations thereof.
    [062] The modification/coating/covalent cross-linking of cellulose, as disclosed, in addition to increasing its hydrophobicity, can also increase its tensile strength and flexibility, thereby further expanding its spectrum of it. All biodegradable and partially biodegradable products made from or using the modified cellulose disclosed in this application are not within the scope of the disclosure.
    [063] Among the possible applications of coating technology, these items include, among others, containers for all purposes, such as boxes, trays, shopping bags, water tubes and conduits, cutlery, dishes and disposable food-grade bottles, TV screens and mobile devices, clothing (eg cotton or cotton blends) and medical devices to be used on or within the body as contraceptives. Also, the coating technology, as disclosed, can be used on furniture and upholstery, outdoor camping equipment and the like.
    [064] The following examples are intended to illustrate and not limit the invention.
    [065] Example 1. Coating of a thin transparent film, made of microfibrillated cellulose (MFC).
    [066] The upper and lower surfaces of a thin transparent film made of microfibrillated cellulose (MFC) were treated with a composition comprising 1 ml of lauroyl chloride (neat) and 1 ml of pyridine (neat) in 20 ml of toluene (neat) ). After coating the film surfaces with a composition, the film was heated to about 110°C for about 3 hours. The sample was subsequently rinsed with acetone and dried. After drying, the sample was evaluated for heat stability, water contact angle, and water vapor transmission rate test (WVTR) at 24 hours, 50°C and 50% RH.
    [067] The sample coating was chemically stable up to about 200°C, and had a contact angle with water of about 100°, which demonstrated that the material was now hydrophobic. Water vapor transmission test results showed superior barrier properties than uncoated film, dirty water permeability was out of scale of the instrument.
    [068] Example 2. Lining of a food tray made of sugarcane bagasse cellulose. .
    [069] A food tray 15 cm by 20 cm in size was treated with its (top) food contact surface with a composition comprising 10 ml of myristoyl bromide (neat) and 10 ml of triethylamine (neat) in 1000 ml of xylene (neat). After coating the surface(s) of the tray with the composition, the tray was heated to about 140°C for about 3 hours. the tray was subsequently rinsed with acetone and dried. After drying, the tray was evaluated for heat stability, water absorption, triglyceride permeability and biodegradable characteristic.
    [070] The tray coating was chemically stable up to about 250°C, and showed no water absorption 30 days after treatment, while remaining completely biodegradable. The tray did not show any permeability to a suspension of triglycerides, even after heating to temperatures above the smoke point for the fat (cocoa butter) itself.
    [071] Example 3. Degree of Tray Lining Replacement
    [072] Tray samples containing cellulose were cut into areas of 3 cm2, weighed, dried in an oven at about 100°C, then weighed again. The samples were coated in 20 ml of dioxane plus 1 ml of pyrimidine and 1 ml of myristoyl chloride, and refluxed for 10 minutes. Subsequently, samples were washed in water:acetone, then dried again and weighed. The results are shown in Table 1.
    * For myristoyl, replacement of about 0.03 (ie about 3%).
    [073] The average degree of substitution of OH with the hydrophobic coating was determined to be about 0.68 (ie, about 70%). See Table 2.


    [074] Although the invention has been described with reference to the above examples, it will be understood that modifications and variations are encompassed within the spirit and scope of the invention. Likewise, the invention is limited only by the following claims. All references disclosed herein are hereby incorporated by reference in their entirety.
    权利要求:
    Claims (17)
    [0001]
    1. Method for treating a solid surface of a cellulose-containing material, characterized in that it comprises: applying to said solid surface a composition comprising: an alkanoic acid derivative having the formula (I):R-CO-X Formula ( I), wherein R is a straight-chain, branched-chain, or cyclic aliphatic hydrocarbon radical having from 10 to 40 carbon atoms, and wherein X is Cl, Br, or O(CO)OR, a base, and a first solvent; heating the composition applied to said solid surface; rinsing said solid surface with a second solvent; drying said rinsed surface, wherein said composition esterifies at least a portion of the available hydroxyl groups through the cellulose of the material, and wherein the resulting treated surface of the cellulose-containing material exhibits a contact angle with water between 60° and 120° °.
    [0002]
    2. Method according to claim 1, characterized in that the material containing cellulose exhibits greater hydrophobicity in relation to the material containing cellulose without said treatment.
    [0003]
    3. Method according to claim 1, characterized by the fact that the base is non-nucleophilic.
    [0004]
    4. Method according to claim 3, characterized by the fact that the base is organic.
    [0005]
    5. Method according to claim 4, characterized in that the organic base is selected from the group consisting of aziridines, azetidines, piperazines, piperidines, pyridines, bipyridines, terpyridines, dihydropyridines, morpholines, N-alkylmorpholines, 1,4-diazabicoclo[2.2.2]octanes, 1,8-diazabicycloundecanes, 1,8-diazabicycloundecenes, dimethyl pentylamines, trimethyl pentylamines, pyrimidines, pyrroles, pyrrolidines, pyrrolidinones, indoles, indolines, indanones, benzindazoles, imidazoles, imidazoles imidazolones, imidazolines, oxazoles, isoxazoles, oxazolines, oxadiazoles, thiadiazoles, carbazoles, quinolines, isoquinolines, naphthyridines, triazines, triazoles, tetrazoles, triethylamines, pyrazoles, pyrasolines, and combinations thereof.
    [0006]
    6. Method according to claim 4, characterized in that the number of carbon atoms is 12 or 14.
    [0007]
    7. Method according to claim 1, characterized in that the first solvent is selected from the group consisting of pentane, hexane, heptane, octane, petroleum ether, naphtha, kerosene, petroleum, paraffin oil, benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, methylene chloride, chloroform, 1,2-dichloroethane, chlorobenzene, carbon tetrachloride, tetrabromoethylene, cyclopentane, cyclohexane, methylcyclohexane, anisole (methyl phenyl ether), methyl tert. - butyl, dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, diisopropyl ether, 1,2-dimethoxyethane (DME, monoglyme), acetone, diisobutyl ketone, methyl-n-propyl ketone; methyl ethyl ketone, methyl isobutyl ketone, methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, and combinations thereof and, wherein the second solvent is selected from the group consisting of pentane, hexane, heptane, octane, petroleum ether, naphtha, kerosene, petroleum, paraffin oil, benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, methylene chloride, chloroform, 1,2-dichloroethane, chlorobenzene, tetrachloride carbon, tetrabromoethylene, cyclopentane, cyclohexane, methylcyclohexane, anisole (methyl phenyl ether), methyl tert-butyl ether, dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, diisopropyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether (diglyme), diethylene glycol monobutyl ether, diethylene glycol monomethyl ether, 1,2-dimethoxyethane (DME, monoglyme), ethylene glycol monobutyl ether, triethylene glycol dimethyl ether (triglyme), triethylene glycol monomethyl ether, acetone, diisobutylketone, m ethyl-n-propyl ketone; methyl ethyl ketone, methyl isobutyl ketone, methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, and combinations thereof.
    [0008]
    8. Method according to claim 1, characterized in that the cellulose-based material comprises a cellulose selected from the group consisting of nanocellulose, cellulose nanofibers, hair crystals or microfibril, microfibrillated cellulose or nanofibril, cellulose of sugarcane bagasse, and combinations thereof.
    [0009]
    9. Method according to claim 1, characterized in that the cellulose-containing material is selected from the group consisting of a food storage box, a shopping bag, eating utensil, container for holding hot drinks or bottles, cup, plate, a food storage bag, a carbonated liquid storage bottle, a non-carbonated liquid storage bottle, food wrapping film, a garbage disposal container, a food handling implement, a fabric fiber, a water storage and transport implement, a storage and transport implement for alcoholic or non-alcoholic beverages, an outer casing or screen for electronic products, an inner or outer piece of furniture, a curtain, upholstery and combinations of same.
    [0010]
    10. Method for treating a solid surface of a cellulose-containing material, according to claim 1, characterized in that it comprises: applying to said solid surface a composition comprising: an alkanoic acid derivative having the formula (I): R -CO-X Formula (I), wherein R is a straight-chain, branched-chain, or cyclic aliphatic hydrocarbon radical having from 10 to 40 carbon atoms, and wherein X is Cl, Br, or O(CO)OR, a base, and a first solvent; heating the composition applied to said solid surface; rinsing said solid surface with a second solvent; drying said rinsed surface, wherein said composition esterifies at least a portion of the available hydroxyl groups via the cellulose of the material, and wherein the resulting treated surface of the cellulose-containing material exhibits a water contact angle of 100°.
    [0011]
    11. Method according to claim 10, characterized in that said composition esterifies at least a portion of the hydroxyl groups available in the cellulose of the material and in that said esterified hydroxyl groups are stable up to at least 200 °C .
    [0012]
    12. Method according to claim 10, characterized in that the base is selected from the group consisting of ammonium hydroxide, potassium hydroxide, sodium hydroxide, sodium carbonate, sodium bicarbonate, hydroxide of lithium, potassium carbonate, aziridines, azetidines, piperazines, piperidines, pyridines, bipyridines, terpyridines, dihydropyridines, morpholiportins, N-alkylmorpholines, 1,4-diazabicyclo[2.2.2]octanes, 1,8-diazabicycloundecanes, 1 and , triazines, triazoles, tetrazoles, triethylamines, pyrazoles, pyrasolines, and combinations thereof.
    [0013]
    13. Method according to claim 10, characterized in that the first solvent is selected from the group consisting of pentane, hexane, heptane, octane, petroleum ether, naphtha, kerosene, petroleum, paraffin oil, benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, methylene chloride, chloroform, 1,2-dichloroethane, chlorobenzene, carbon tetrachloride, tetrabromoethylene, cyclopentane, cyclohexane, methylcyclohexane, anisole (methyl phenyl ether), methyl tert-butyl ether , dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, diisopropyl ether, 1,2-dimethoxyethane (DME, monoglyme), acetone, diisobutyl ketone, methyl-n-propyl ketone; methyl ethyl ketone, methyl isobutyl ketone, methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, and combinations thereof and, wherein the second solvent is selected from the group consisting of pentane, hexane, heptane, octane, petroleum ether, naphtha, kerosene, petroleum, paraffin oil, benzene, toluene, xylene, mesitylene, ethylbenzene, diethylbenzene, methylene chloride, chloroform, 1,2-dichloroethane, chlorobenzene, tetrachloride carbon, tetrabromoethylene, cyclopentane, cyclohexane, methylcyclohexane, anisole (methyl phenyl ether), methyl tert-butyl ether, dibenzyl ether, diethyl ether, dioxane, diphenyl ether, vinyl methyl ether, tetrahydrofuran, diisopropyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether (diglyme), diethylene glycol monobutyl ether, diethylene glycol monomethyl ether, 1,2-dimethoxyethane (DME, monoglyme), ethylene glycol monobutyl ether, triethylene glycol dimethyl ether (triglyme), triethylene glycol monomethyl ether, acetone, diisobutyl ketone, m ethyl-n-propyl ketone; methyl ethyl ketone, methyl isobutyl ketone, methyl formate, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, and combinations thereof.
    [0014]
    14. Method according to claim 13, characterized in that the number of carbon atoms is 12 or 14.
    [0015]
    15. Method according to claim 10, characterized in that the cellulose-based material comprises a cellulose selected from the group consisting of nanocellulose, cellulose nanofibers, hair crystals or microfibril, microfibrillated cellulose or nanofibril, bagasse cellulose of cane, and combinations thereof.
    [0016]
    16. Method for treating a solid surface of a cellulose-containing material, according to claim 10, characterized in that it comprises: applying to said solid surface a composition comprising: an alkanoic acid derivative having the formula (I): R-CO-X Formula (I), wherein R is a straight-chain, branched-chain, or cyclic aliphatic hydrocarbon radical having from 10 to 40 carbon atoms, and wherein X is Cl, Br, or O(CO)OR a base, and a first solvent; heating the composition applied to said solid surface; rinsing said solid surface with a second solvent; and drying said rinsed surface, wherein said composition esterifies at least a portion of the available hydroxyl groups via the cellulose of the material, and wherein the resulting treated surface of the cellulose-containing material exhibits a water contact angle of 100°, it is stable up to at least 200°C, an oxygen permeability of less than 10 Barrer units, a water vapor permeability of less than 20 Barrer units, and combinations thereof.
    [0017]
    17. Method according to claim 16, characterized in that the number of carbon atoms is 12 or 14.
    类似技术:
    公开号 | 公开日 | 专利标题
    BR112014032259B1|2021-06-08|method for treating a solid surface of a cellulose-containing material
    JP2015533858A5|2016-08-12|
    US11098134B2|2021-08-24|Methods for biobased derivatization of cellulosic surfaces
    AU2006253520B2|2010-09-23|Gas barrier laminate, method for producing same and package body using same
    Wu et al.2020|Water and humidity-induced shape memory cellulose nanopaper with quick response, excellent wet strength and folding resistance
    Vuoti et al.2013|Solvent impact on esterification and film formation ability of nanofibrillated cellulose
    Kim et al.2019|Crab-on-a-tree: all biorenewable, optical and radio frequency transparent barrier nanocoating for food packaging
    ES2436366T3|2013-12-30|Biologically degradable material of a polymer containing porous organometallic structural material
    CN109968755A|2019-07-05|Biodegradable composite package film and packaging bag
    Bedane et al.2014|Water vapor adsorption equilibria and mass transport in unmodified and modified cellulose fiber-based materials
    Habel et al.2018|High‐Barrier, Biodegradable Food Packaging
    BR0108620B1|2010-11-30|process for the preparation of a barrier coating, treated substrate and barrier coating composition.
    CA3136320A1|2020-10-22|Method of modifying polymer barrier films
    Jha et al.2020|Effect of Amylose–Amylopectin Ratios on Physical, Mechanical, and Thermal Properties of Starch‐Based Bionanocomposite Films Incorporated with CMC and Nanoclay
    WO2016040228A1|2016-03-17|Enhanced cellulosic materials
    OA16693A|2015-12-07|
    JP2008049606A|2008-03-06|Biodegradable gas-barrier material
    Kaldéus et al.2018|One-pot preparation of bi-functional cellulose nanofibrils
    Khouri2019|Chitosan Edible Films Crosslinked by Citric Acid
    JP2022500550A|2022-01-04|Bio-based barrier coating
    JP2015004029A|2015-01-08|Functional film
    JPH09194667A|1997-07-29|Polyvinyl alcohol composition and its production
    JP2001300306A|2001-10-30|Carbon dioxide adsorbent
    JP3713964B2|2005-11-09|Bag for bag in box
    WO2021019468A1|2021-02-04|Hemicellulose-containing coatings
    同族专利:
    公开号 | 公开日
    EP2864544B1|2020-01-01|
    NI201400154A|2015-07-16|
    ZA201500024B|2016-10-26|
    CO7180205A2|2015-02-09|
    CL2014003520A1|2015-06-12|
    MX2015000117A|2015-09-21|
    CU20140147A7|2015-04-29|
    US20130345415A1|2013-12-26|
    CA2877201A1|2014-01-03|
    US20150148532A1|2015-05-28|
    CN104540995B|2017-08-29|
    US20160083546A1|2016-03-24|
    EP3628775B1|2021-12-15|
    EA201492254A1|2015-07-30|
    UA115446C2|2017-11-10|
    JP2015533858A|2015-11-26|
    IN2014DN11084A|2015-09-25|
    CR20150017A|2016-02-29|
    AU2013282930A1|2015-01-22|
    US9139661B2|2015-09-22|
    EP2864544A1|2015-04-29|
    WO2014001874A1|2014-01-03|
    PH12014502885A1|2015-02-23|
    KR20150034202A|2015-04-02|
    US20150368364A1|2015-12-24|
    NZ703331A|2017-07-28|
    AP2015008196A0|2015-01-31|
    US20160355609A1|2016-12-08|
    DOP2014000296A|2015-03-31|
    IL236382D0|2015-02-26|
    EP3628775A1|2020-04-01|
    SG11201408605UA|2015-01-29|
    PE20150899A1|2015-06-27|
    AU2013282930B2|2016-11-24|
    CU24268B1|2017-07-04|
    BR112014032259A2|2017-06-27|
    ECSP15002496A|2016-01-29|
    CN104540995A|2015-04-22|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3894839A|1972-09-21|1975-07-15|Us Of Amercia As Represented B|Process for acylating functional groups bearing active hydrogen with isopropenyl esters of long chain fatty acids|
    US4107426A|1976-07-06|1978-08-15|Roy Gerald Gordon|Process for treating cellulose|
    JPS623272B2|1979-02-16|1987-01-23|Kyodo Printing Co Ltd|
    US4374702A|1979-12-26|1983-02-22|International Telephone And Telegraph Corporation|Microfibrillated cellulose|
    JPH0470047B2|1988-06-04|1992-11-09|Asahi Chemical Ind|
    EP0706766B1|1994-09-22|2002-08-14|Daicel Chemical Industries, Ltd.|A tobacco filter material and a method for producing the same|
    JP3454584B2|1994-10-18|2003-10-06|ダイセル化学工業株式会社|Filter for tobacco smoke and method for producing the same|
    FR2767270B1|1997-08-14|2000-02-11|Daniel Gamain|GAS PHASE TREATMENT PROCESS OF A SOLID MATERIAL TO MAKE IT HYDROPHOBIC, MATERIAL OBTAINED AND APPLICATIONS|
    KR100626129B1|1999-06-22|2006-09-20|데이진 가부시키가이샤|Magnetic recording medium and base film therefor|
    JP4149676B2|2001-02-05|2008-09-10|株式会社東芝|Photomask correction method|
    EP1696972B1|2003-12-19|2016-10-26|Buckeye Technologies Inc.|Fibers of variable wettability and materials containing the fibers|
    US20080265222A1|2004-11-03|2008-10-30|Alex Ozersky|Cellulose-Containing Filling Material for Paper, Tissue, or Cardboard Products, Method for the Production Thereof, Paper, Tissue, or Carboard Product Containing Such a Filling Material, or Dry Mixture Used Therefor|
    US20090135345A1|2005-12-12|2009-05-28|Takatoshi Yajima|Polarizing Plate Protective Film, Film Producing Method, Polarizing Plate, and Liquid Crystal Display|
    DE07709298T1|2006-02-08|2014-01-30|Stfi-Packforsk Ab|Process for the preparation of microfibrillated cellulose|
    WO2008090795A1|2007-01-26|2008-07-31|Konica Minolta Holdings, Inc.|Organic electroluminescent device, display device and illuminating device|
    WO2010039865A2|2008-10-01|2010-04-08|Cornell University|Biodegradable chemical delivery system|
    US9371616B2|2009-01-05|2016-06-21|Konica Minolta Holdings, Inc.|Laminate and production method thereof|
    US9139661B2|2012-06-25|2015-09-22|Yagna Limited|Methods for biocompatible derivitization of cellulosic surfaces|US9139661B2|2012-06-25|2015-09-22|Yagna Limited|Methods for biocompatible derivitization of cellulosic surfaces|
    JP6120590B2|2013-02-01|2017-04-26|国立大学法人京都大学|Modified nanocellulose and resin composition containing modified nanocellulose|
    WO2016020866A1|2014-08-06|2016-02-11|Basf Se|Method for the continuous coating of a cellulose-based fibrous substrate web with fatty acid chloride|
    WO2016040228A1|2014-09-08|2016-03-17|Humanitarian Scientific Llc|Enhanced cellulosic materials|
    RU2690278C2|2014-10-20|2019-05-31|Филип Моррис Продактс С.А.|Hydrophobic tipping paper|
    TWI682727B|2014-12-23|2020-01-21|瑞士商菲利浦莫里斯製品股份有限公司|Hydrophobic rolling paper|
    WO2016131790A1|2015-02-18|2016-08-25|Basf Se|Method for manufacturing of a hydrophobic cellulosic material|
    JP6640623B2|2016-03-18|2020-02-05|国立大学法人京都大学|Masterbatch containing acylated modified microfibrillated plant fibers|
    JP2017190541A|2016-04-14|2017-10-19|凸版印刷株式会社|Barrier paper, manufacturing method thereof and paper cup|
    SG11201901751QA|2016-09-01|2019-03-28|Hs Mfg Group Llc|Methods for biobased derivatization of cellulosic surfaces|
    EP3594301A4|2017-03-07|2020-12-23|Kao Corporation|Film comprising hydrophobized cellulose fibers and oil|
    KR101975977B1|2017-10-20|2019-05-09|전자부품연구원|Method of hydrophobic treatment of cellulose fiber and hydrophobic cellulose fiber produced by the treatment method|
    FR3075071B1|2017-12-20|2020-09-18|Centre Technique Du Papier|PROCESS FOR CONFERRING A HYDROPHOBIC CHARACTER ON A SOLID SUBSTRATE CONTAINING REACTIVE HYDROPHILIC FUNCTIONS|
    CN108951285A|2018-08-02|2018-12-07|宁波高新区诠宝绶新材料科技有限公司|A kind of preparation method of Neutral Papermaking polymeric material|
    KR20200071504A|2018-12-11|2020-06-19|전자부품연구원|A surface modification method of cellulose and a surface modified cellulose|
    WO2020178798A1|2019-03-06|2020-09-10|Greentech Global Pte. Ltd.|Liquid dispersions for acyl halides|
    SE1950871A1|2019-07-08|2021-01-09|Stora Enso Oyj|Paper or paperboard material comprising one or more plies|
    SE543479C2|2019-07-09|2021-03-02|Stora Enso Oyj|Bio-barrier coated paperboard and laminates thereof|
    CN111206317B|2020-03-17|2021-01-29|阜阳恒泰纺织有限公司|Modified flax/viscose blended yarn and preparation method thereof|
    CN112321729A|2020-12-03|2021-02-05|安徽森淼实业有限公司|Preparation method of hydroxypropyl methyl cellulose|
    法律状态:
    2018-03-27| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-04-10| B25A| Requested transfer of rights approved|Owner name: HUMANITARIAN SCIENTIFIC LLC. (US) |
    2019-04-24| B08F| Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]|Free format text: REFERENTE A 6A ANUIDADE. |
    2019-12-31| B08G| Application fees: restoration [chapter 8.7 patent gazette]|
    2020-02-27| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2021-04-06| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-06-08| 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 25/06/2013, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    US13/531,939|US9139661B2|2012-06-25|2012-06-25|Methods for biocompatible derivitization of cellulosic surfaces|
    US13/531,939|2012-06-25|
    PCT/IB2013/001342|WO2014001874A1|2012-06-25|2013-06-25|Methods for biodegradable derivatization of cellulosic surfaces|
    [返回顶部]