Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B23/00—Layered products comprising a layer of cellulosic plastic substances, i.e. substances obtained by chemical modification of cellulose, e.g. cellulose ethers, cellulose esters, viscose
  • B32B23/04—Layered products comprising a layer of cellulosic plastic substances, i.e. substances obtained by chemical modification of cellulose, e.g. cellulose ethers, cellulose esters, viscose comprising such cellulosic plastic substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B23/08—Layered products comprising a layer of cellulosic plastic substances, i.e. substances obtained by chemical modification of cellulose, e.g. cellulose ethers, cellulose esters, viscose comprising such cellulosic plastic substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B27/10—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
  • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
  • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B29/00—Layered products comprising a layer of paper or cardboard
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
  • B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B82—NANOTECHNOLOGY
  • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
  • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
  • C08L1/02—Cellulose; Modified cellulose
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
  • D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
  • D21H11/18—Highly hydrated, swollen or fibrillatable fibres
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • D21H19/00—Coated paper; Coating material
  • D21H19/10—Coatings without pigments
  • D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
  • D21H19/34—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising cellulose or derivatives thereof
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • D21H19/00—Coated paper; Coating material
  • D21H19/80—Paper comprising more than one coating
  • D21H19/82—Paper comprising more than one coating superposed
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
  • B32B2262/06—Vegetal fibres
  • B32B2262/062—Cellulose fibres, e.g. cotton
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2307/00—Properties of the layers or laminate
  • B32B2307/70—Other properties
  • B32B2307/724—Permeability to gases, adsorption
  • B32B2307/7242—Non-permeable
  • B32B2307/7244—Oxygen barrier
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2307/00—Properties of the layers or laminate
  • B32B2307/70—Other properties
  • B32B2307/724—Permeability to gases, adsorption
  • B32B2307/7242—Non-permeable
  • B32B2307/7246—Water vapor barrier
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2439/00—Containers; Receptacles
  • B32B2439/70—Food packaging
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
  • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
  • B65D5/00—Rigid or semi-rigid containers of polygonal cross-section, e.g. boxes, cartons or trays, formed by folding or erecting one or more blanks made of paper
  • B65D5/42—Details of containers or of foldable or erectable container blanks
  • B65D5/56—Linings or internal coatings, e.g. pre-formed trays provided with a blow- or thermoformed layer
  • B65D5/563—Laminated linings; Coatings

Definitions

• Multilayer film comprising microfibrillated cellulose
• the present invention relates to a method of manufacturing a fibrous-based oxygen barrier film.
• the invention further covers films made by the method and uses thereof.
• microfibrillated cellulose Today, films comprising microfibrillated cellulose (MFC), have proven to give excellent barrier properties, see e.g. Aulin et al., Oxygen and oil barrier properties of microfibrillated cellulose films and coatings, Cellulose (2010) 17:559-574, Lavoine et al., Microfibrillated cellulose - Its barrier properties and applications in cellulosic materials: A review, Carbohydrate polymers 90 (2012) 735-764, Kumar et al., Comparison of nano- and microfibrillated cellulose films, Cellulose (2014) 21 :3443-3456. However, the gas barrier properties are very dependent on the moisture or the relative humidity in the surrounding environment.
• a first layer (1 ) comprising at least 80 % by weight of microfibrillated cellulose (MFC) as calculated on the total solid content of said layer,
• MFC microfibrillated cellulose
• a third layer (3) comprising at least 40 %, preferably at least 50 %, by weight of chemically modified microfibrillated cellulose as calculated on the total solid content of said layer.
• the film of the invention has shown to provide excellent gas barrier properties, especially oxygen barrier properties, also at high humidity and also good strength properties.
• the second layer further comprises pigments.
• a second layer comprising a polymer and pigments decreases the moisture and oxygen transmission rate even further.
• the film may have a basis weight of less than 50 g/m 2 , such as 10 - 50 g/m 2 and an Oxygen Transmission Rate (OTR) value of below 10 ml/m 2 /per 24h, preferably below 5 ml/m 2 /per 24h, at 23 Q C, at 50% RH.
• OTR Oxygen Transmission Rate
• the film may exhibit an OTR value of below 20 ml/m 2 per 24h or preferably of below 10 ml/ m 2 per 24h, at 23 Q C.
• the film may exhibit an OTR value of below 100 ml/m 2 per 20h, at 38 Q C.
• the first layer made from a composition comprising a high amount of MFC, provides strength and strain to the structure.
• the second layer comprising a polymer and optionally pigments, provides protection of the third layer by decreasing the moisture and oxygen transmission rate through the film.
• the third layer including chemically modified MFC, provides oxygen barrier properties even at high or fluctuating humidity.
• the oxygen barrier properties of said third layer is rendered more stable with time when combined with said first and second layer.
• said chemically modified MFC is dialdehyde
• microfibrillated cellulose D-MFC
• Said third layer may further comprise at least 10 %, preferably at least 15 % by weight of unmodified microfibrillated cellulose.
• said third layer is made from a mixture of chemically modified microfibrillated cellulose and un modified microfibrillated cellulose. It has been shown that mixtures of chemically modified microfibrillated cellulose and un-modified microfibrillated cellulose give rise to a stable particle size distribution after storage and consequently better barrier properties when formed to a film.
• the oxygen barrier film further comprises
• a fourth layer (4) comprising a polymer and optionally pigments
• microfibrillated cellulose as calculated on the total solid content of said layer.
• the third layer forms a middle layer whereby the first and second layers are arranged on one side of said middle layer and said fourth and fifth layers are arranged on the opposite side of said middle layer.
• a film provides equal barrier properties on both sides and can thus also advantageously be used as a self-standing film.
• the polymer present in the second layer is chosen from the group consisting of polyvinyl alcohol (PVOH), latex, CMC, starch, guar gum and/or waxes.
• the pigments are preferably nanopigments.
• the nanopigments are platy and may have an aspect ratio of at least 90:1 or at least 100:1.
• the second layer comprising polymers and such platy pigments, provides an efficient mechanical barrier to moisture.
• nanopigments swell in contact with moisture and thereby improves the barrier properties of the film even further.
• a method of manufacturing a film as described above comprising the steps of a) forming a first layer comprising microfibrillated cellulose b) forming a second layer comprising a polymer and optinally pigments on one side of said first layer
• the method may further comprise the steps of forming a fourth layer comprising a polymer and optionally pigments on the third layer and forming a fifth layer comprising MFC on said fourth layer.
• Said layers may be formed by cast forming and/or by spraying.
• Microfibrillated cellulose shall in the context of the patent application mean a nano scale cellulose particle fiber or fibril with at least one dimension less than 100 nm.
• MFC comprises partly or totally fibrillated cellulose or lignocellulose fibers.
• the liberated fibrils have a diameter less than 100 nm, whereas the actual fibril diameter or particle size distribution and/or aspect ratio (length/width) depends on the source and the manufacturing methods.
• the smallest fibril is called elementary fibril and has a diameter of approximately 2- 4 nm (see e.g.
• Chinga-Carrasco G., Cellulose fibres, nanofibrils and microfibrils,: The morphological sequence of MFC components from a plant physiology and fibre technology point of view, Nanoscale research letters 201 1, 6:417), while it is common that the aggregated form of the elementary fibrils, also defined as microfibril ( Fengel , D., Ultrastructural behavior of cell wall polysaccharides, Tappi J., March 1970, Vol 53, No. 3.), is the main product that is obtained when making MFC e.g. by using an extended refining process or pressure-drop disintegration process. Depending on the source and the manufacturing process, the length of the fibrils can vary from around 1 to more than 10 micrometers. A coarse MFC grade might contain a substantial fraction of fibrillated fibers, i.e. protruding fibrils from the tracheid (cellulose fiber), and with a certain amount of fibrils liberated from the tracheid (cellulose fiber).
• MFC cellulose microfibrils, fibrillated cellulose, nanofibrillated cellulose, fibril aggregates, nanoscale cellulose fibrils, cellulose nanofibers, cellulose nanofibrils, cellulose microfibers, cellulose fibrils, microfibrillar cellulose, microfibril aggregrates and cellulose microfibril aggregates.
• MFC can also be characterized by various physical or physical- chemical properties such as large surface area or its ability to form a gel-like material at low solids (1 -5 wt%) when dispersed in water.
• the cellulose fiber is preferably fibrillated to such an extent that the final specific surface area of the formed MFC is from about 1 to about 300 m 2 /g, such as from 1 to 200 m 2 /g or more preferably 50-200 m 2 /g when determined for a freeze- dried material with the BET method.
• MFC multi-pass refining
• pre-hydrolysis followed by refining or high shear disintegration or liberation of fibrils.
• One or several pre-treatment step is usually required in order to make MFC manufacturing both energy efficient and sustainable.
• the cellulose fibers of the pulp to be supplied may thus be pre-treated enzymatically or chemically.
• the nanofibrillar cellulose may contain some hemicelluloses; the amount is dependent on the plant source.
• Mechanical disintegration of the pre-treated fibers, e.g. hydrolysed, pre-swelled, or oxidized cellulose raw material is carried out with suitable equipment such as a refiner, grinder, homogenizer, colloider, friction grinder, ultrasound sonicator, fluidizer such as microfluidizer, macrofluidizer or fluidizer-type homogenizer.
• suitable equipment such as a refiner, grinder, homogenizer, colloider, friction grinder, ultrasound sonicator, fluidizer such as microfluidizer, macrofluidizer or fluidizer-type homogenizer.
• the product might also contain fines, or nanocrystalline cellulose or e.g. other chemicals present in wood fibers or in papermaking process.
• the product might also contain various amounts of micron size fiber particles that have not been efficiently fibrillated.
• MFC is produced from wood cellulose fibers, both from hardwood or softwood fibers. It can also be made from microbial sources, agricultural fibers such as wheat straw pulp, bamboo, bagasse, or other non-wood fiber sources. It is preferably made from pulp including pulp from virgin fiber, e.g. mechanical, chemical and/or thermomechanical pulps. It can also be made from broke or recycled paper.
• MFC includes, but is not limited to, the new proposed TAPPI standard W13021 on cellulose nanofbril (CNF) defining a cellolose nanofbire material containing multiple elementary fibrils with both crystalline and amorphous regions, having a high aspect ratio with width of 5- 30nm and aspect ratio usually greater than 50.
• CNF cellulose nanofbril
• “Chemically modified microfibrillated cellulose” as used throughout the description and in the claims shall in this context mean microfibrillated cellulose fibers that are chemically modified before or after fibrillation so that they contain functional groups other (or more) than found in the original cellulose. Such groups include, among others, carboxymethyl (CMC), aldehyde and/or carboxyl groups (cellulose obtained by N-oxyl mediated oxydation, for example "TEMPO”), or quaternary ammonium (cationic cellulose).
• “Un-modified microfibrillated cellulose” shall in this context mean microfibrillated cellulose fibers that have not been chemically modified to contain functional groups other (or more) than found in the original cellulose.
• OTR oxygen transmission rate
• Figure 1 discloses a film according to one embodiment of the invention.
• the multilayer film (10) disclosed in fig. 1 comprises a first layer (1 ) comprising microfibrillated cellulose, a second layer (2) comprising a polymer and optionally pigments and a third layer (3) comprising chemically modified microfibrillated cellulose.
• the second layer is arranged on (and preferably in direct contact with) the first layer and the third layer is arranged on (and preferably in direct contact with) the second layer.
• the first layer (1 ) has a thickness of between 5 - 25 pm, preferably 15 - 25 pm
• the second layer (2) has a thickness of between 0.1 - 15 pm, most preferably of between 2 - 10 pm
• the third layer (3) has a thickness of between of between 5 - 25 pm, most preferably of between 5 - 15 pm.
• the first layer (1 ) comprises microfibri Hated cellulose in an amount of at least 80 % by weight, preferably in an amount of at least 90 % by weight or even at least 95 % by weight, as calculated on the total solid content of said layer.
• said MFC is unmodified MFC. Further additives may be e.g.
• fillers pigments, wet strength chemicals, retention chemicals, cross-linkers, softeners or plasticizers, adhesion primers, wetting agents, biocides, optical dyes, fluorescent whitening agents, defoaming chemicals, hydrophobizing chemicals such as AKD, ASA, waxes, resins etc.
• the second layer (2) comprises a polymer and optionally pigments.
• Said polymer may be chosen from the group consisting of polyvinylalcohol (PVOFI), latex, starch, guar gum and/or wax.
• PVOFI polyvinylalcohol
• the second layer is preferably formed from a dispersion comprising pigments and the polymer.
• the said layer may preferably comprise 0 - 30 wt% pigments, or 5 - 30 wt%, more preferably 10 - 20 wt% pigments as calculated on the total dry weight of said second layer, the remains being polymer such as PVOFI.
• the pigments are preferably nanopigments.
• nanopigment is defined as inorganic pigments having a weigh median diameter (d50) of less than 100 nm.
• the pigment may e.g. be clay such as kaolin clay, calcium carbonate, talc.
• the pigment is montmorillonite clay, kaolinite
• Said third layer may comprise at least 75 wt% or at least 80 wt%, or at least 95 wt% of microfibrillated cellulose, whereof at least a part is chemically modified microfibrillated cellulose.
• the third layer comprises at least 40 wt%, or at least 50 wt%, at least 60 or even at least 75 wt% of chemically modified cellulose.
• the third layer further comprises unmodified microfibrillated cellulose in an amount of at least 10wt% or at least 20 wt%.
• the third layer comprises between 40 - 80 wt% chemically modified microfibrillated cellulose and between 30 - 10 wt% unmodified microfibrillated cellulose and between 30 - 10 wt% of an additive. All percentages calculated based on the total solid content of said layer.
• Said additive may e.g. be any one of a starch, carboxymethyl cellulose, a filler, retention chemicals, flocculation additives, deflocculating additives, dry strength additives, softeners or mixture thereof.
• the chemically modified microfibrillated cellulose used in the invention is preferably dialdehyde microfibrillated cellulose (DA-MFC).
• D-MFC dialdehyde microfibrillated cellulose
• the microfibrillated dialdehyde cellulose should in this context mean a dialdehyde cellulose treated in such way that it is microfibrillated.
• the microfibrillated dialdehyde cellulose may be produced by treating dialdehyde cellulose for example by a homogenizer or in any other way such that fibrillation occurs to produce microfibrillated dialdehyde cellulose.
• the microfibrillated dialdehyde cellulose has an oxidation degree between 20-75%, preferably between 30-65%, even more preferably between 30-50% or most preferred between 35-45%.
• the degree of oxidation was determined according to the following description: after the dialdehyde cellulose reaction, the amount of C2-C3 bonds in the cellulose that are converted to dialdehydes are measured. The degree of oxidation is the amount of C2-C3 bonds that are converted compared to all C2-C3 bonds. This is measured with a method by H. Zhao and N.D. Heindel,“Determination of Degree of Substitution of Formyl Groups in Polyaldehyde Dexran by the Hydroxylamine Hydrochloride Method”, Pharmaceutical Research, vol. 8, pp. 400-402, 1991 , where the available aldehyde groups reacts with hydroxylamine hydrochloride. This forms oxime groups and releases hydrochloric acid.
• the hydrochloric acid is titrated with sodium hydroxide until pH 4 is reached, and the degree of oxidation is thereafter calculated from according to the formula below.
• the received aldehyde content is divided by two to get the value of the degree of oxidation, since an oxidized anhydroglucose unit has two aldehyde groups.
• ITIsample dry weight of the analysed DAC sample (g)
• M w 160 g/mol, which is the molecular weight of the dialdehyde cellulose unit
• a suspension comprising microfibrillated cellulose
• a porous surface is e.g. a wire in a paper machine.
• the fibrous web can then be dried in a drying section in a paper machine to form the MFC film.
• the suspension comprising MFC
• the non-porous surface may e.g. be a plastic or metal belt on which the suspension is evenly distributed through a slot or sprayed and the MFC film is formed during drying.
• the MFC film is then peeled off from the supporting medium in order to form a stand-alone film.
• the multilayer film of the invention can be manufactured by use of cast forming, wire forming and/or spraying.
• the first layer is formed by cast forming a suspension comprising microfibrillated cellulose and possible additives at a consistency of between 3 - 30 %, preferably between 5 - 20 %, onto a non-porous surface to form a web. Said web is thereafter at least partly dried to form a first film layer having a first and a second side.
• a dispersion comprising a polymer and optionally pigments is casted or sprayed onto the first side of said first film to form a second film having a first and a second side.
• the third layer is formed by casting or spraying a suspension comprising chemically modified microfibrillated cellulose onto the first side of said second film, which is finally dried to form a multilayer film.
• the multilayer film formed by the method described has preferably a basis weight of less than 50 g/m2, such as between 10 - 50 g/m2, more preferably of 20 - 40 g/m2, or 20 - 30 g/m 2 and a thickness preferably of below 70 pm or below 50 pm, preferably in the range of 20 - 40 pm.
• the density of the film may be in the range of from 750 kg/m 3 to 1550 kg/m 3 .
• the density is higher than 750 kg/m 3
• the density is higher than 950 kg/m 3
• the density is higher than 1050 kg/m 3 .
• the film may thus be a so called dense film.
• a final paper- or board product comprising the film according to the present invention may comprise several layers.
• the product has the following structure: board or paper/third layer/second layer/first layer, i.e. the layers are the following: a layer of a conventional board or paper material, a layer comprising DA-MFC, a layer comprising polymers and pigments and a layer comprising MFC.
• the film may be used as a layer on a paperboard to provide a barrier layer on a liquid packaging board (instead of the al layer).
• Figure 2 shows another embodiment of the invention, wherein the reference numbers (1 ), (2) and (3) correspond to the reference numbers described in connection with Figure 1.
• the multilayer film (20) further comprises a forth layer (4) comprising a polymer and optionally pigments and a fifth layer (5) comprising microfibrillated cellulose.
• the forth layer (4) may be identical to the second layer (2) and said fifth layer (5) may be identical to the first layer (1 ).
• the forth layer can be formed by spraying or casting a dispersion comprising a polymer and pigments onto the formed third layer (3) with subsequent drying to form a fourth layer. Thereafter a suspension comprising microfibrillated fibers may be casted or sprayed onto the forth layer, which is subsequently dried to form the multilayer film.
• the multilayer film disclosed in this embodiment may be used as a self standing film, e.g. in packaging of food, but may also be applied on a paper or board substrate. Further layers, e.g. polymer layer such as polyethylene (PE), may be applied in-between the paper- or board substrate and said film comprising said three or five layers, as well as on the outer, opposite surface of the film.
• PE polymer layer
• PE polyethylene
• the product has the following structure: Board or paper substrate/PE/third layer/second layer/first layer/PE, or
• the product has the following structure: Board- or paper substrate/PE/fifth layer/forth layer/third layer/second layer/first layer/PE, or PE/board- or paper substrate/PE/fifth layer/forth layer/third layer/second layer/first layer/PE.
• the paperboard may first be provided with a PE layer on both a first side and on a second side, preferably by extrusion coating. Thereafter, the film according to the first embodiment (including the first, second and third layer) or the second embodiment (including the first, second, third, fourth and fifth layer) may be applied, e.g.
• the paperboard may be provided with an additional PE layer ontop of the laminated film.
• This structure is particularly suitable for use in liquid packaging.
• the film of the invention may thus replace an aluminum foil layer normally applied as liquid barrier on the inner side of the packaging board.
• Example - Making an MFC film with protecting layer to improve oxygen transmission rate
• a film (Sample 1 ) and a reference film (Reference 1 ) were prepared.
• Sample 1 was a three layered film containing 100 wt% native MFC in the carrying layer, 91 wt% PVOH and 9 wt% bentonite in the protecting middle layer and 80 wt% DA-MFC with a degree of oxidation of 40% and 20 wt% native MFC in the barrier layer.
• Reference 1 was a two layered film were the protecting middle layer in Sample 1 was left out.
• the carrier layer had 100% native MFC and the barrier layer consisted of 80 wt% DA-MFC with a degree of oxidation of 40% and 20 wt% native MFC.
• the PVOFI grade used in the example had a viscosity of 12.5-17.5 mPa * s of a 4% aqueous solution at 20 °C, DIN 53015 / JIS K 6726 and a hydrolysis degree of 99%.
• the bentonite was Na-Cloisite.
• Polyvinyl alcohol was jet cooked for 2 h at a solid content of 14 wt%. It was thereafter diluted to 7%.
• the bentonite clay was mixed with high shear rate for
• a mixture of MFC and DA-MFC was prepared by mixing 80% of a dialdehyde cellulose (DAC) which had a degree of oxidation of 40% with 20 wt% of native MFC. The mixing time was 1 h. Afterwards, the mixture was run 3 passages in a Microfluidizer M-1 10EH, resulting in a DA-MFC-MFC suspension. The solids content was 2,7 wt%. The suspension was deaerated for one hour in a vacuum assisted mixing. . This mix was used for both Sample 1 and Reference 1 as the barrier layer.
• DAC dialdehyde cellulose
• the film according to the invention (Sample 1 ) was produced by rod coating the DA-MFC/MFC mixture on a substrate held at a temperature of 60 Q C, whereupon the PVOFI/bentonite mixture was applied as a thin layer by use of a brush. Thereafter the Native MFC mixture was rod-coated onto the
• the reference film (Reference 1 ) was produced by rod coating Native MFC mixture on a substrate held at a temperature 80 Q C, followed by rod-coating of the DA-MFC/MFC mixture.
• Reference 1 and Sample 1 were tested with respect to the OTR at a relative humidity of 50 % and 80% at 23 °C according to ASTM F- 1927. The results are shown in Table 1 below.
• the oxygen barrier properties of the film of the invention were improved at 50% humidity.
• the OTR of the inventive film was initially slightly higher, but the increase of OTR with time at the end of the measurement (24h) was remarkably lower.

Landscapes

• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Manufacturing & Machinery (AREA)
• Health & Medical Sciences (AREA)
• Nanotechnology (AREA)
• Composite Materials (AREA)
• General Physics & Mathematics (AREA)
• Crystallography & Structural Chemistry (AREA)
• Condensed Matter Physics & Semiconductors (AREA)
• Physics & Mathematics (AREA)
• Laminated Bodies (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=65409114

Family Applications (1)

Country Status (4)

Families Citing this family (8)

Family Cites Families (10)

• 2017
  • 2017-12-22 SE SE1751637A patent/SE542054C2/en not_active IP Right Cessation
• 2018
  • 2018-12-21 EP EP18847151.0A patent/EP3727849A1/en not_active Withdrawn
  • 2018-12-21 WO PCT/IB2018/060496 patent/WO2019123405A1/en unknown
  • 2018-12-21 JP JP2020533700A patent/JP2021507830A/ja not_active Abandoned

Also Published As

Similar Documents

Legal Events