WO2022229518A1 - Couche barrière pour substrat cellulosique - Google Patents
Couche barrière pour substrat cellulosique Download PDFInfo
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- WO2022229518A1 WO2022229518A1 PCT/FR2022/000030 FR2022000030W WO2022229518A1 WO 2022229518 A1 WO2022229518 A1 WO 2022229518A1 FR 2022000030 W FR2022000030 W FR 2022000030W WO 2022229518 A1 WO2022229518 A1 WO 2022229518A1
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- 229920000642 polymer Polymers 0.000 claims description 45
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- -1 alkaline earth metal carbonates Chemical class 0.000 claims description 42
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 7
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
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- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 4
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- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
- C08F220/286—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety and containing polyethylene oxide in the alcohol moiety, e.g. methoxy polyethylene glycol (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/10—Copolymers of styrene with conjugated dienes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/14—Copolymers of styrene with unsaturated esters
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- 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
- D21H19/36—Coatings with pigments
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
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- D21H19/00—Coated paper; Coating material
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- D21H19/38—Coatings with pigments characterised by the pigments
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- 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
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids 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
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/52—Additives of definite length or shape
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0081—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/02—Compounds of alkaline earth metals or magnesium
- C09C1/021—Calcium carbonates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/40—Compounds of aluminium
- C09C1/42—Clays
Definitions
- the invention relates to the field of the protection of sensitive substances by means of a barrier layer applied to a cellulosic substrate.
- the cellulosic substrate is usually paper or cardboard. It is coated by means of a barrier layer composition.
- the invention provides an aqueous mineral suspension and an aqueous composition for preparing a barrier layer which comprise a polymeric stabilizing agent and prepared from (meth)acrylic acid and a polyalkoxylated methacrylic derivative.
- the cellulosic substrate is generally made of paper or cardboard and is intended for the packaging of foodstuffs.
- the application of a barrier layer provides protection by reducing the migration of aqueous, organic or aromatic liquids as well as the migration of gases (e.g. oxygen, water vapor, aromas). Migration phenomena can occur from the external environment towards packaged foodstuffs or occur for packaged foodstuffs towards the external environment. Very often, the packaged goods are foodstuffs.
- barrier layers in particular for the coating of cellulosic substrates.
- Such barrier layers must be able to prevent or slow down the penetration of at least one substance through the cellulosic substrate.
- the barrier layer must be able to block at least one gaseous, liquid or solid substance.
- this barrier layer must be able to block water, alcohols, natural oils, mineral oils, gases such as water vapour, O 2 , CO 2 , fats, organic solvents, flavorings or perfumes.
- barrier properties are particularly sought after for preparing barrier layers for a cellulosic substrate, in particular for a cellulosic substrate of natural origin or of plant origin or else for a composite or mixed cellulosic substrate.
- the cellulosic substrates for which such barrier layers are particularly useful are new paper obtained from new cellulose fibers, new cardboard obtained from new cellulose fibers, recycled paper or recycled cardboard, mainly obtained from recycled paper or cardboard.
- cellulosic substrates coated by means of an effective barrier layer in particular for a cellulosic substrate in the form of a container, a packaging, in particular a container or a packaging food, a non-food container or packaging, a container or packaging for medicine, a container or packaging for an oxidisable substance, a container or packaging for hygroscopic substance.
- the barrier layer can protect the substance included in the packaging or in the container.
- the barrier layer can also make it possible to prevent the substance, or some of its liquid or gaseous, aqueous or organic components, packaged or contained in the packaging or in the container, from leaving it or migrating through the packaging. , and thus prevent this substance from coming into contact with the environment outside the coated cellulosic substrate.
- barrier layers based on plastic polymers are generally available, the use of which should be avoided or limited, in particular for environmental reasons.
- barrier layers based on mineral pigments combined with a binding agent it is now preferable to use barrier layers based on mineral pigments combined with a binding agent.
- barrier layer compositions combining mineral pigment and binding agent regularly lead to the appearance of defects on the barrier layer affixed to the cellulosic substrate. The most common defects take the form of scratches or uneven, incomplete or interrupted areas of the barrier layer.
- Barrier layer defects originate from the formation or growth of agglomerates of particles in the composition for preparing the barrier layer or in the mineral suspension for preparing this composition. Indeed, as soon as such agglomerates of particles form or have a size comparable to the thickness of the barrier layer, they can generate numerous defects during the application of the barrier layer to the surface of the cellulosic substrate.
- Document EP 2777934 describes barrier layer preparation compositions for multilayer packaging comprising a water vapor barrier layer covered with a gas barrier layer. These compositions can comprise a sodium polyacrylate. Furthermore, documents FR 2846978, FR 2917091 and US 20110305915 describe the preparation of paper coating slips comprising a pigment, a binder latex and various polymeric additives.
- compositions for preparing a barrier layer and the known mineral suspensions for preparing these compositions do not make it possible to provide an effective and satisfactory solution to these problems.
- the invention provides a barrier layer preparation composition and a mineral suspension for preparing this composition which make it possible to provide a solution to all or part of the problems of barrier layer preparation compositions and mineral suspensions for preparing these the state of the art.
- the invention provides an aqueous mineral suspension S for preparing an aqueous barrier layer composition C for a cellulosic substrate, comprising water and, relative to the total quantity of dry active ingredients of the suspension, a . 5 to 34.9% by dry weight of at least one inorganic pigment (a) chosen from alkaline earth metal carbonates, magnesium carbonate, barium carbonate, dolomite, kaolin, titanium dioxide, talc, lime, sulphate calcium, barium sulphate, hexacalcium hexaoxotris-(sulphato-(2-)-dialuminate-(12-) (satin white), silica and combinations thereof; b.
- inorganic pigment chosen from alkaline earth metal carbonates, magnesium carbonate, barium carbonate, dolomite, kaolin, titanium dioxide, talc, lime, sulphate calcium, barium sulphate, hexacalcium hexaoxotris-(sulphato-(2-)
- At least one binding agent (b) chosen from a binding agent (b1) in the form of a latex prepared by emulsion-polymerization and a polymeric binding agent (b2) in the form of an aqueous dispersion and combinations thereof; c. 0.1 to 2 % by dry weight of at least one stabilizer (c) prepared by at least one polymerization reaction
- R 1 independently represents H or a C3 ⁇ 4 group
- - L 1 independently represents oxyethylene (OE) groups or a combination of OE groups and oxypropylene (OP) groups;
- - n independently represents an integer or decimal number between 20 and 200.
- the aqueous suspension S according to the invention comprises four essential components. Besides water, the suspension S includes three types of active ingredients: the pigment (a), the agent (bl) or the agent (b2) and the stabilizing agent (c). According to the invention and unless otherwise indicated, the quantities of active ingredients are expressed in quantities of dry ingredient.
- the suspension S is an aqueous suspension.
- the active ingredients are therefore mixed with water.
- this aqueous suspension S comprises an amount by weight of water of approximately 50% relative to the total weight of the aqueous suspension S. Nevertheless, depending on the conditions of preparation or implementation of this aqueous suspension S, the amount of water may vary.
- the aqueous suspension S can comprise 30% by weight or 40% by weight of water but also up to 60% by weight or up to 70% by weight of water. Most of the water in the S-suspension comes from the water used as the support medium.
- a fraction of the water in the aqueous suspension S comes from the water used to support or to shape one or the other of the active ingredients, in particular the water of the latex of the agent (bl), the water of the dispersion of the binding agent (b2) or the water which can be used as a support for the pigment (a) or the water which can be used as a support for the stabilizing agent (c).
- the stabilizing agent (c) makes it possible to control or reduce the size of the agglomerates of particles which may be present or which may form within the suspension S or else in a barrier layer composition for a cellulosic substrate prepared using this suspension S.
- agent (c) makes it possible to eliminate or reduce the size of the agglomerates of particles of mineral pigment (a) or of particles of binding agent (b). According to the invention the agent (c) therefore makes it possible to control or improve the homogeneity of a barrier layer on a cellulosic substrate.
- the suspension S comprises a pigment (a) chosen from natural calcium carbonate, precipitated calcium carbonate, kaolin, calcined kaolin, talc, titanium dioxide and combinations thereof.
- the preferred pigment (a) according to the invention is calcium carbonate, optionally combined with kaolin or talc.
- the suspension S comprises a pigment (a) in the form of particles, preferably particles whose size is less than 10 ⁇ m or else having a size ranging from 0.05 ⁇ m to 10 ⁇ m or else a size of less than 8 ⁇ m, preferably less than 5 ⁇ m or less than 2 ⁇ m, more preferably less than 1 ⁇ m or less than 0.5 ⁇ m.
- the suspension S comprises a pigment (a) in the form of particles whose equivalent spherical diameter, for a size ranging from 0.05 ⁇ m to 10 ⁇ m or less than 10 ⁇ m, preferably for a size of less than 8 ⁇ m, more preferably less than 5 ⁇ m or less than 2 ⁇ m or less than 0.3 ⁇ m, even more preferably less than 1 ⁇ m or less than 0.5 ⁇ m or even less than 0.3 ⁇ m, is equal to 60% by weight or equal to 70% by weight or even equal to 80% by weight or even equal to 90% by weight.
- the particle size measurement is carried out by laser diffraction measurement.
- the pigment (a) may be surface-treated or may not comprise any surface treatment.
- the pigment (a) can be surface-treated hydrophobically.
- Fatty acids for example stearic acid, ricinoleic acid, palmitic acid, can be used to treat the surface of the pigment (a).
- Other substances can be used for the surface treatment of the pigment (a), for example, surface-active compound, modified hydrophobic polymer, styrene-acrylic resin emulsion, styrene-butadiene latex emulsion, styrene-acrylic mixture and styrene latex, silane, siloxane, siloxane-silicone resin combination.
- the binding agent (b) is an essential active ingredient of the suspension S according to the invention.
- the suspension S according to the invention comprises a binding agent (b1) which is in the form of a binding latex prepared by emulsion-polymerization of at least one ethylenically unsaturated monomer.
- the binding agent (bl) is prepared from a monomer selected from styrene, ethylene, butadiene, vinyl acetate, carboxylic acids comprising ethylenic unsaturation (more preferably acrylic acid and methacrylic acid), acrylic acid ester, methacrylic acid ester, acrylamide, methacrylamide, acrylonitrile, methacrylonitrile, ester acrylonitrile, methacrylonitrile ester and combinations thereof.
- the suspension S according to the invention comprises a binding agent (bl) which is in the form of a binding latex prepared by emulsion-polymerization
- At least one additional monomer chosen from fumaric acid, itaconic acid, maleic acid, fumaric acid ester, itaconic acid ester, maleic acid ester, silanes, siloxanes and their combinations.
- the suspension S according to the invention comprises a binding agent (bl) chosen from acrylic latexes, carboxylated styrene-butadiene latexes, non-carboxylated styrene-butadiene latexes, styrene-acrylate latexes, styrene-butyl acrylate latexes, butadiene-methyl methacrylate latex, butadiene-acrylonitrile latex, polyvinyl acetate latex and combinations thereof.
- bl binding agent chosen from acrylic latexes, carboxylated styrene-butadiene latexes, non-carboxylated styrene-butadiene latexes, styrene-acrylate latexes, styrene-butyl acrylate latexes, butadiene-methyl methacrylate latex, butadiene-acrylonitrile latex, polyvin
- the suspension S according to the invention comprises a binder (b2) which is chosen from aqueous dispersions of binder polymers chosen from polyethylenes (PE), polypropylenes (PP), ethylenevinyl acetate polymers (EVA), ethylene polymers - acrylic acid (EAA), ethylene-methacrylic acid polymers (EMAA), ethylene-butyl acrylate polymers (EBA), ethylene-methyl acrylate polymers (EMA), styrene-isoprene block copolymers (SIS), styrene-butadiene block copolymers (SBS) ), styrene-ethylene-butylene (SEBS) block polymers, ethylene copolymers modified with acrylic acid, polyvinyl alcohols, modified polyvinyl alcohols, preferably EAA, EVA, SBS.
- binder polymers chosen from polyethylenes (PE), polypropylenes (PP), ethylenevinyl acetate polymers (EVA), ethylene polymers
- the suspension S comprises at least one binding agent (b). It can be used alone or can be combined with at least one other binding agent (b').
- the binding agent (b') is of natural origin. Preferably, it is a binding agent (b') chosen from carboxymethyl celluloses, starches, modified starches, proteins, caseins, alginates and their combinations.
- the stabilizing agent (c) is an essential active ingredient of the suspension S according to the invention.
- the suspension S according to the invention comprises an agent (c) which is a polymer prepared by a polymerization reaction of at least one monomer (cl) chosen from acrylic acid, methacrylic acid and combinations thereof.
- the suspension S according to the invention comprises an agent (c) which is a polymer prepared by a polymerization reaction of at least one monomer (c2) of formula I in which L 1 represents OE.
- the stabilizing agent (c) can be used in its acid form.
- the agent (c) is totally or partially neutralized.
- Agent (c) can be neutralized by means of a compound chosen from NaOH, KOH, LiOH, Mg(OH)2, Ca(OH)2, ZnO, CaO, MgO, ammonium derivatives, ammonia, amino bases, by example triethanolamine, aminomethylpropanol or 2-amino-2-methyl-propanol (AMP) and their combinations, in particular NaOH or KOH combined with Ca(OH)2 or with Mg(OH)2.
- NaOH and KOH are preferred.
- agent (c) has a weight-average molecular mass Mw measured by steric exclusion chromatography (SEC) of less than 40000000 g/mol, preferably less than 20000000 g/mol or less at 15,000,000 g/mol, more preferably less than 1,0000,000 g/mol or less than 5,000,000 g/mol. Also preferably according to the invention, agent (c) has a weight-average molecular mass Mw measured by steric exclusion chromatography (SEC) greater than 100,000 g/mol or greater than 300,000 g/mol or greater than 500,000 g/mol or even greater than 1,000,000 g/mol.
- SEC steric exclusion chromatography
- agent (c) has a weight-average molecular mass Mw measured by steric exclusion chromatography (SEC) ranging from 1,000,000 g/mol to 5,000,000 g/mol. Also preferably according to the invention, agent (c) has an IP polydispersity index measured by steric exclusion chromatography (SEC) of less than 2.8 or an IP polydispersity index ranging from 1.5 to 3, from 1.5 to 2.8 or ranging from 1.5 to 2.5.
- the agent (c) can be prepared by a polymerization reaction implementing other compounds.
- the agent (c) can be prepared by a polymerization reaction using at least one additional monomer (c3), different from the monomers (cl) and (c2), chosen from maleic acid, anhydride maleic acid, itaconic acid, 2-acrylamido-2-methylpropane sulfonic acid (AMPS), 2-acrylamido-2- methylpropane sulfonic acid, vinylsulfonic acid, 2-(methacryloyloxy)-ethanesulfonic acid, 2-(methacryloyloxy)-ethanesulfonic acid, methallyl sulfonate sodium, styrene sulfonate and their salts, preferably itaconic acid, 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and their salts.
- AMPS 2-acrylamido-2-methylpropane sulfonic acid
- the agent (c) can be prepared by a polymerization reaction using at least one additional monomer, different from the monomers (cl) and (c2), which is a compound (c4) of formula (II ): in which :
- - L 2 independently represents an OE group or a combination of OE and OP groups
- - m independently represents an integer or decimal number between 10 and 150, preferably between 20 and 75;
- - OE independently represents an oxyethylene group
- - OP independently represents an oxypropylene group.
- the agent (c) can be prepared by a polymerization reaction using at least one additional monomer, different from the monomers (cl) and (c2), which is a monomer (c5) of formula (III ): in which : - L 3 independently represents an OE group or a combination of OE and OP groups;
- - u independently represents an integer or decimal number between 10 and 150, preferably between 20 and 75;
- - OE independently represents an oxyethylene group
- - OP independently represents an oxypropylene group
- - R 2 independently represents H or CH3.
- the agent (c) can be prepared by a polymerization reaction implementing at least one additional monomer, different from the monomers (cl) and (c2), which is a monomer (c6) of formula (IV ): in which :
- - L 4 independently represents an OE group
- - OE independently represents an oxyethylene group
- - v independently represents an integer or decimal number between 10 and 150, preferably between 20 and 75.
- the agent (c) can be prepared by a polymerization reaction using at least one additional monomer, different from the monomers (cl) and (c2), which is a monomer (c6a) of formula (V ): in which :
- - L 5 independently represents an OE group
- - OE independently represents an oxyethylene group
- - w independently represents an integer or decimal number between 10 and 150, preferably between 20 and 75.
- the agent (c) can be prepared by a polymerization reaction using at least one additional monomer, different from the monomers (cl) and (c2), which is a compound (c7) of formula (VI ): in which :
- - L 6 independently represents an OE group or a combination of OE and OP groups
- - t independently represents an integer or decimal number between 10 and 150, preferably between 20 and 75;
- - OE independently represents an oxyethylene group
- - OP independently represents an oxypropylene group.
- the stabilizing agent (c) according to the invention makes it possible to act on the stability of the suspension S according to the invention.
- agent (c) can act on the formation of agglomerates of particles or on the growth of agglomerates of particles which could form in the suspension S.
- the agglomerates of particles which can form in the suspension S according to the invention could be agglomerates of pigment particles (a), agglomerates of binder particles (b) or else agglomerates of composite particles of binder (b) and pigment (a).
- the suspension S has a concentration of agglomerates of size greater than 20 ⁇ m, measured by laser diffraction, which is less than 10% by volume.
- the suspension S has a concentration of agglomerates of size greater than 10 ⁇ m, measured by laser diffraction, which is less than 30% by volume.
- the suspension S does not comprise any agglomerate of a size greater than 100 ⁇ m, or even does not comprise any agglomerate of a size greater than 80 ⁇ m or of a size greater than 70 ⁇ m.
- the suspension S according to the invention has a pH greater than 5, preferably greater than 5.5, more preferably greater than 6 or 6.5. Also preferably, the suspension S has a pH lower than 13 or lower than 12. More preferably, the suspension S has a pH ranging from 5 to 13 or from 5 to 12 or from 5 to 11, preferably ranging from 5.5 to 13 or from 5.5 to 12 or from 5.5 to 11, more preferably ranging from 6 to 13 or from 6 to 12 or from 6 to 11, also more preferably from 7 to 13 or from 7 to 12 or 7 to 11, in particular 7.5 to 10.
- the amounts of ingredients may vary.
- the suspension S comprises, relative to the total quantity of dry active ingredients of the suspension, a.
- the suspension S comprises, relative to the total quantity of dry active ingredients of the suspension, a. 10 to 29.9% by dry weight or 15 to 29.9% by dry weight of mineral pigment (a); b. 70 to 88% by dry weight or 70 to 83% by dry weight of binding agent (b) and c. 0.1 to 2% by dry weight of agent (c).
- the suspension S comprises, relative to the total quantity of dry active ingredients of the suspension, a. 10 to 24.9% by dry weight or 15 to 24.9% by dry weight of mineral pigment (a); b. 75 to 88% by dry weight or 75 to 83% by dry weight of binding agent (b) and c. 0.1 to 2% by dry weight of agent (c).
- the suspension S according to the invention can be used to prepare an aqueous composition useful for preparing a barrier layer for a cellulosic substrate.
- the invention provides an aqueous composition C for preparing a barrier layer for a cellulosic substrate, comprising, relative to the total amount of composition,
- e chosen from ASE polymers, HASE polymers and combinations thereof.
- the ASE and HASE polymers used according to the invention are known as such.
- ASE polymers Alkali-Soluble Emulsions or Alkali-Swellable Emulsions
- HASE polymers Hydrophobically modified Alkali-Soluble Emulsions or Hydrophobically modified Alkali-Swellable Emulsions
- hydrophobically modified copolymers which are soluble or swellable in an alkaline medium.
- the aqueous composition C comprises a thickening agent (e) which is an ASE polymer prepared by at least one polymerization reaction
- At least one monomer (e2) chosen from Ci-Cs esters of a compound derived from an acid chosen from acrylic acid, methacrylic acid and combinations thereof.
- the aqueous composition C comprises a thickening agent (e) which is a HASE polymer prepared by at least one polymerization reaction
- - OE independently represents an oxyethylene group (CH2CH2O)
- - OP independently represents an oxypropylene group (CH(CH 3 )CH 2 0 or CH 2 CH(CH )0),
- R 3 represents a group comprising at least one polymerizable olefinic unsaturation, preferably chosen from acrylate, methacrylate, acrylurethane, methacrylurethane, vinyl, allyl, methallyl, isoprenyl, a-a'-dimethyl-isopropenyl-benzylurethane, allylurethane, ester of maleic acid, itaconic acid ester, crotonic acid ester, more preferably methacrylate,
- R 4 represents a C ô -C40-alkyl group, linear or branched, a phenyl group, a polyphenyl group, preferably a Cio-C30-alkyl group, linear or branched, more preferably a Ci2-C22-alkyl group, linear or branched, or a group comprising 2 to 5 phenyl groups or a tristyrylphenyl group or a pentastyrylcumylphenyl group.
- the ASE polymer is prepared by at least one polymerization reaction which implements:
- the HASE polymer is prepared by at least one polymerization reaction which implements:
- the ASE polymer or the HASE polymer can be prepared by at least one polymerization reaction which also implements at least a different additional monomer (e4).
- the monomer (e4) is chosen from 2-acrylamido-2-methylpropane sulphonic acid, ethoxymethacrylate sulphonic acid, sodium methallyl sulphonate, styrene sulphonate phosphated hydroxyethyl-acrylate, phosphated hydroxypropyl-acrylate , phosphated hydroxyethyl methacrylate, phosphated hydroxypropyl methacrylate, their salts and their combinations; preferably less than 20 mol%, preferably 0.2 to 20 mol%, in particular 0.5 to 10 mol%, of monomer (e4) relative to the total molar quantity of monomers.
- the ASE polymer or the HASE polymer can also be prepared by at least one polymerization reaction which also uses at least one different additional monomer (e5) chosen from hydroxyethyl-acrylate, hydroxypropyl-acrylate, hydroxyethylhexyl-acrylate, hydroxyethyl-methacrylate, hydroxypropyl-methacrylate; preferably less than 20% molar, preferably from 0.2 to 20 molar %, in particular from 0.5 to 10 molar %, of monomer (e5) relative to the total molar quantity of monomers.
- additional monomer e5 chosen from hydroxyethyl-acrylate, hydroxypropyl-acrylate, hydroxyethylhexyl-acrylate, hydroxyethyl-methacrylate, hydroxypropyl-methacrylate; preferably less than 20% molar, preferably from 0.2 to 20 molar %, in particular from 0.5 to 10 molar %, of monomer (e5)
- the ASE polymer or the HASE polymer can also be prepared by at least one polymerization reaction which also uses at least one different additional crosslinking monomer (e6) or at least one monomer (e6) comprising at least two olefinic unsaturations; preferably less than 5% molar, preferably from 0.01 to 4% molar, in particular from 0.02 to 4% molar or from 0.02 to 2% molar, in particular from 0.02 to 1% molar, of monomer (e6) relative to the total molar quantity of monomers.
- at least one polymerization reaction which also uses at least one different additional crosslinking monomer (e6) or at least one monomer (e6) comprising at least two olefinic unsaturations; preferably less than 5% molar, preferably from 0.01 to 4% molar, in particular from 0.02 to 4% molar or from 0.02 to 2% molar, in particular from 0.02 to 1% molar, of monomer (e6) relative to the total molar quantity
- agent (e) can be used directly or it can be used in a neutralized form.
- agent (e) can be totally or partially neutralized, preferably by means of at least one compound chosen from NaOH, KOH, LiOH, Mg(OH)2, Ca(OH)2, ZnO, CaO , MgO, ammonium derivatives, ammonia, amino bases, for example triethanolamine, aminomethylpropanol or 2-amino-2-methyl-propanol (AMP) and their combinations, in particular NaOH or KOH combined with Ca(OH)2 or Mg(OH) 2.
- NaOH and KOH are preferred
- agent (e) according to the invention can also be coacervated. It can be totally or partially coacerbated.
- agent (e) can be coacervated by reducing the pH, for example by reducing the pH to a value below 6.5.
- the pH reduction can be carried out by means of an acid compound, in particular by means of at least one organic or mineral acid compound, in particular an acid compound chosen from phosphoric acid, citric acid, glucono-lactone, lactic acid, acid salicylic acid, glycolic acid, ascorbic acid, glutamic acid, hydrochloric acid, acetic acid, D-gluconic acid, sulfonic acid, methane-sulfonic acid, benzimidazole-sulfonic acid, tartaric acid, 4-aminobenzoic acid, benzoic acid, sorbic acid, acid phenylbenzimidazole sulfonic, benzylidene camphor sulfonic acid, terephthalylidene dicamphor sulfonic acid, kojic acid, hyaluronic acid.
- an acid compound chosen from phosphoric acid, citric acid, glucono-lactone, lactic acid, acid salicylic acid, glycolic acid, ascorbic acid
- Agent (e) can also be coacervated by increasing the ionic strength, for example by adding at least one ionized compound or at least one salt, in particular NaCl, KC1, MgCl 2 , CaCl 2 , MgS0 4 , CaS0 4 .
- the stabilizing agent (c) and the ASE or HASE polymers used according to the invention are known as such. They can be prepared by known methods, in particular a radical polymerization reaction, for example a polymerization reaction in emulsion, in dispersion or in solution.
- the polymerization can be carried out in a solvent, in the presence of at least one initiator compound.
- initiator compounds use may be made of at least one compound chosen from azo initiator compounds (for example azo-bis-isobutyronitrile), a peroxide compound, preferably hydrogen peroxide, benzoyl peroxide, benzoyl hydroperoxide and mixtures thereof. .
- alkali metal persulfates in particular sodium persulfate and potassium persulfate, ammonium persulfate, partially water-soluble peroxides, in particular succinic peracid, t-butyl hydroperoxide, t-butyl hydroperoxide, cumyl, persulphates associated with a cuprous ion, a ferrous ion, a sulphite ion or a bisulphite ion and mixtures thereof.
- the method for preparing these polymers generally uses at least one chain transfer agent, preferably chosen from mercaptan compounds, in particular mercaptan compounds comprising at least four carbon atoms such as butyl mercaptan, n-octylmercaptan, n-dodecylmercaptan, tert-dodecylmercaptan, isooctyl 3-mercaptopropionate.
- the reaction is a free radical emulsion polymerization reaction.
- the compound initiator or generator of radicals can therefore be combined with at least one transfer agent for controlled radical polymerization, in particular a transfer agent of the RAFT type (reversible addition-fragmentation chain transfer or radical polymerization controlled by transfer of reversible chain by addition-fragmentation).
- RAFT reversible addition-fragmentation chain transfer or radical polymerization controlled by transfer of reversible chain by addition-fragmentation
- the aqueous composition C has a pH greater than 5, preferably greater than 5.5, more preferably greater than 6 or 6.5.
- composition C has a pH below 11 or below 10.5. More preferably, composition C has a pH ranging from 4 to 13 or from 4 to 12 or from 4 to 11, preferably ranging from 5 to 13 or from 5 to 12 or from 5 to 11, more preferably ranging from 6 to 13 or from 6 to 12 or from 6 to 11, also more preferably ranging from 6.5 to 13 or from 6.5 to 12 or from 6.5 to 11, in particular from 7.5 to 9.5.
- the thickening agent (e) is an essential ingredient of the aqueous composition C according to the invention. It is effective in thickening this composition by modifying its rheology. This results in an increase in the viscosity of the aqueous composition C according to the invention.
- the aqueous composition C according to the invention has a Brookfield viscosity measured at 25° C. at a speed of 100 revolutions/min greater than 100 mPa.s.
- composition C has a Brookfield viscosity measured at 25° C. at a speed of 100 rpm ranging from 100 to 3000 mPa.s or from 100 to 2500 mPa.s or from 200 to 3000 mPa.s or from 200 to 2500 mPa. s.
- the composition C generally has a concentration of agglomerates of size greater than 20 ⁇ m , measured by laser diffraction, which is less than 10% by volume. Also preferably according to the invention, composition C has a concentration of agglomerates of size greater than 10 ⁇ m, measured by laser diffraction, which is less than 30% by volume. Particularly preferably according to the invention, composition C does not comprise an agglomerate of a size greater than 100 ⁇ m, or even does not comprise an agglomerate of a size greater than 80 ⁇ m or of a size greater than 70 ⁇ m.
- a first preparation method according to the invention makes it possible to prepare a suspension S by mixing the active ingredients (a), (b) and (c) in water.
- the suspension S is prepared by mixing in water, relative to the total quantity of dry active ingredients of the suspension,
- the invention also provides a method for preparing composition C by mixing the suspension S and the thickening agent (e) and optionally water.
- the method for preparing the aqueous barrier layer composition C for a cellulosic substrate comprises: a. the preparation of an aqueous mineral suspension S according to the invention by mixing in water, relative to the total quantity of dry active ingredients of the suspension,
- the method for preparing the aqueous barrier layer composition C for a cellulosic substrate comprises: has. the preparation of an aqueous mineral suspension S according to the invention by mixing in water, relative to the total quantity of dry active ingredients of the suspension,
- composition C of at least one thickening agent (e) according to the invention.
- the aqueous composition C according to the invention makes it possible to prepare a barrier layer on a cellulosic substrate.
- the invention therefore provides a method for preparing a barrier layer for a cellulosic substrate comprising the application of at least one aqueous composition C according to the invention on at least one surface of a cellulosic substrate.
- this method according to the invention is implemented by application of the aqueous composition C of barrier layer produced by coating.
- the coating is carried out by means of coating rollers (for example Size Press, Metering Size Press) or scraping metering systems (for example by pencil or by blade) or non-contact metering systems (for example with blade air or by curtain).
- the coating may also be applied in several successive steps using one or more of the coating means. We will then apply a pre-coat preceding one or more top coats whose compositions may be different.
- this method according to the invention is such that the barrier layer is resistant to at least one substance chosen from water, alcohols, natural oils, mineral oils, gases (water vapour, O2, CO2), greases, organic solvents, aromas, perfumes.
- this method makes it possible to control, slow down or stop the migration through the cellulosic substrate of at least one substance chosen from water, alcohols, natural oils, mineral oils, gases (water vapour, O2, CO2), fats, organic solvents, aromas, perfumes.
- the barrier prepared by means of composition C according to the invention makes it possible to act on the exchange kinetics between the interior and exterior environments of the cellulosic substrate covered by means of this layer.
- the transfer kinetics of a particular substance is sufficiently slowed down, or even significantly stopped, to constitute a barrier to this substance between the internal medium and the external medium of the barrier layer.
- the cellulosic substrate is of natural origin or of vegetable origin or is a composite or mixed cellulosic substrate. More preferably, the cellulosic substrate is chosen from new paper, new cardboard, recycled paper, recycled cardboard and combinations thereof. Also preferably, the coated cellulosic substrate is in the form of a container, a wrapper.
- it is a food container, a food packaging, a non-food container, a non-food packaging, a medicine container, a medicine packaging , container for oxidizable substance, packaging for oxidizable substance, container for hygroscopic substance, packaging for hygroscopic substance.
- paper and cardboard are mainly made up of virgin cellulose fibers from paper pulp, possibly mixed with recovered fibers from recycled paper or recycled cardboard.
- the cellulosic substrate can also comprise mineral pigments, process adjuvants or functional adjuvants giving it the optical properties, printability or the desired mechanical properties.
- aqueous compositions C according to the invention make it possible to define aqueous compositions C according to the invention which are also advantageous, particular or preferred.
- the invention provides various advantageous, particular or preferred methods which are defined by the advantageous, particular or preferred characteristics of the aqueous suspension S according to the invention.
- the molecular weight of the copolymers is determined by Steric Exclusion Chromatography (SEC).
- SEC Steric Exclusion Chromatography
- This technique uses a Waters brand liquid chromatography apparatus equipped with two detectors. One combines light scattering at a 90° angle with viscometry measured by a Viscotek Malvem detector viscometer. The other is a Waters refractometric concentration detector.
- This liquid chromatography apparatus is equipped with steric exclusion columns chosen to separate the different molecular weights of the polymers studied.
- the liquid elution phase is an aqueous phase containing 1% KNO3.
- the polymerization solution is diluted to 0.9% dryness in the eluent of the CES, which is a 1% KNO3 solution.
- the liquid chromatography apparatus contains an isocratic pump (Waters 515) whose flow rate is set at 0.8mL/min.
- the chromatography apparatus also comprises an oven comprising the following column system in series: a guard column of the Guard Column Ultrahydrogel Waters type (6 cm in length and 40 mm in internal diameter), a linear column of the Ultrahydrogel Waters type (30 cm in length and 7.8 mm internal diameter) and two Ultrahydrogel 120 A columns (30 cm long and 7.8 mm internal diameter).
- the detection system consists of a refractometric detector of the RI Waters 410 type and a double viscometer and light scattering detector at an angle of 90° of the 270 Dual Detector Malvem type.
- the oven is brought to a temperature of 55°C and the refractometer is brought to a temperature of 45°C.
- the chromatography device is calibrated by a single poly-ethoxylate standard (19000 g/mol) of the PolyCal Malvem type.
- the pH is measured at 25° C. with a WTW brand pH meter equipped with a conventional electrode coupled to a temperature probe.
- the Brookfield viscosity of the compositions prepared is measured at 100 revolutions/min and at 25°C.
- the mobile is chosen according to the viscosity of the composition considered in order to be in the optimal range of use of the rheometer.
- the particle sizes are measured using a Malvem Mastersizer 3000 laser particle sizer.
- the method and the instrument are known as such and are commonly used to determine the grain size of mineral fillers, pigments or polymers.
- the measurements are carried out in an aqueous solution comprising 0.1% by weight of Na 4 P20 7 . Samples are dispersed using a high speed stirrer and optionally ultrasound.
- a stirred reactor Into a stirred reactor are introduced 490 g of deionized water, 21.45 of acrylic acid, 4.91 g of methacrylic acid and 217.40 g of a monomer c2 of formula I in which RI represents H, L1 represents a combination of 46 oxyethylene (EO) groups and 15 oxypropylene (OP) groups with a molecular weight of 3000 g/mol and the mixture is heated to 64 ⁇ 1°C. Then, a mixture of 10 g of water, 0.66 g of DMDO (2,2′-(ethylenedioxy)diethanethiol) and 2.84 g of monomer c2 as well as a mixture of 15 g of water and 1.03 g of ammonium persulfate.
- RI represents H
- L1 represents a combination of 46 oxyethylene (EO) groups and 15 oxypropylene (OP) groups with a molecular weight of 3000 g/mol
- EO oxyethylene
- the reactor is maintained at a temperature of 65 ⁇ 2° C. for 1 hour 30 minutes. Then, 0.61 g of ammonium persulfate dissolved in 20 g of deionized water are introduced into the reactor. Finally, it is cooked for 1 hour before allowing the medium to cool to room temperature.
- the stabilizing agent cA according to the invention is neutralized by adding an aqueous solution of sodium hydroxide at 50% by mass (16.17 g). Its molecular mass measured by CES is 1,800,000 g/mol.
- a first container of the glass beaker type, 160.77 g of ethyl acrylate, 116.42 g of methacrylic acid, 5.66 g of a compound e3 of formula VII in which q represents 36 , r represents 0, OE independently represents an oxyethylene group (CH2CH2O), R 3 represents a methacrylate group and R 4 represents a branched alkyl group comprising 20 carbon atoms, 1.50 g of sodium dodecyl sulfate and 112 g of deionized water .
- a second container of the glass beaker type, 0.871 g of ammonium persulfate is weighed and dissolved in 10 g of deionized water.
- a third container of the glass beaker type, 0.087 g of sodium metabisulphite is weighed and dissolved in 10 g of deionized water.
- a fourth container of the syringe type, 9.31 g of sodium salt of 2-acrylamido-2-methylpropanesulfonic acid at 50% by weight in water are weighed. The contents of the reactor are heated to a temperature of 76°C ⁇ 2°C. In two hours, the reagents of the 4 containers are introduced into the polymerization reactor at a temperature of 76°C ⁇ 2°C. Then, 0.098 g of ammonium persulfate dissolved in 12 g of deionized water are introduced. Finally, it is cooked for 1 hour before allowing the medium to cool.
- a thickening agent eA according to the invention is obtained at 30.0% by weight of dry extract.
- An aqueous composition Cl according to the invention is prepared by mixing in deionized water:
- binding agent styrene-butadiene latex (Trinseo DL1066 product at ph 7 and 55% by weight of dry extract),
- stabilizing agent c-A in water at 25% by weight of dry extract
- composition C1 - 0.3 part by dry weight of thickening agent eA (in water at 30% by weight of dry extract). The amount of water is adjusted to obtain a dry extract of 49.8% by weight of composition C1.
- a comparative aqueous composition CCI is prepared by mixing in deionized water:
- binding agent styrene-butadiene latex (Trinseo DL1066 product at ph 7 and 55% by weight of dry extract),
- the amount of water is adjusted to obtain a dry extract of 49.8% by weight of the composition CCI.
- a sample of composition C1 and a sample of composition CCI are prepared in order to measure their Brookfield viscosity at 100 revolutions/min at 25° C. Furthermore, a sample of 250 g of composition C1 is prepared and then filtered to separate therefrom the agglomerates whose size is greater than 45 ⁇ m. The quantity of agglomerates separated by the filter is weighed. Similarly, the agglomerates larger than 45 ⁇ m are separated from a sample of 250 g of composition CCI. The measurements are carried out twice for each sample. The results are shown in Table 1.
- the composition C1 according to the invention comprises an extremely small quantity of agglomerates whose size is greater than 45 ⁇ m.
- the comparative composition includes nearly 14 times more agglomerates larger than 45 pm.
- composition Cl and composition CCI are prepared to perform particle size measurements. These measurements are taken in water using a laser particle sizer (Malvem Mastersizer 3000 equipped with a hydro-LV tank) and processed with the Mastersizer 3000 software (refractive index 1.590, adsorption index 0.005, mixer speed : 3000 rpm). The measurements are carried out under red and blue lights. One measurement per aliquot is performed. Three washing cycles are carried out between each series. For each composition and at similar obscuration rates, the particle size is measured and the results of the volume average particle size measurements are presented in Table 2.
- the composition Cl according to the invention comprises a very small fraction (measured by volume) of agglomerates whose size is greater than 18 .50 p.m. Furthermore, the stabilizing agent c-A according to the invention allows a strong limitation of the maximum size of the agglomerates compared to the agglomerates of the comparative composition whose maximum size reaches 211 ⁇ m.
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EP22719966.8A EP4330300A1 (fr) | 2021-04-29 | 2022-04-12 | Couche barrière pour substrat cellulosique |
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FR2104526A FR3122431B1 (fr) | 2021-04-29 | 2021-04-29 | Couche barrière pour substrat cellulosique |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2846978A1 (fr) | 2002-11-08 | 2004-05-14 | Coatex Sas | Utilisation d'un copolymere disposant d'au moins une fonction greffee alkoxy ou hydroxy polyalkylene glycol, comme agent ameliorant l'activation de l'azurage optique et produits obtenus |
FR2917091A1 (fr) | 2007-06-08 | 2008-12-12 | Coatex S A S Soc Par Actions S | Procede de fabrication d'une formulation aqueuse a base de solution d'un polymere peigne acrylique et d'emulsion epaississante acrylique, formulation obtenue et ses utilisations dans le couchage papetier |
US20110305915A1 (en) | 2010-06-10 | 2011-12-15 | Coatex S.A.S. | Hydroxy polyalkylene glycol function (meth) acrylic comb polymers, their use as shear-thinning agents in coating dispersions and dispersions containing them |
EP2777934A1 (fr) | 2011-11-10 | 2014-09-17 | Nippon Paper Industries Co., Ltd | Matériau d'emballage à papier barrière |
-
2021
- 2021-04-29 FR FR2104526A patent/FR3122431B1/fr active Active
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2022
- 2022-04-12 WO PCT/FR2022/000030 patent/WO2022229518A1/fr active Application Filing
- 2022-04-12 EP EP22719966.8A patent/EP4330300A1/fr active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2846978A1 (fr) | 2002-11-08 | 2004-05-14 | Coatex Sas | Utilisation d'un copolymere disposant d'au moins une fonction greffee alkoxy ou hydroxy polyalkylene glycol, comme agent ameliorant l'activation de l'azurage optique et produits obtenus |
FR2917091A1 (fr) | 2007-06-08 | 2008-12-12 | Coatex S A S Soc Par Actions S | Procede de fabrication d'une formulation aqueuse a base de solution d'un polymere peigne acrylique et d'emulsion epaississante acrylique, formulation obtenue et ses utilisations dans le couchage papetier |
US20110305915A1 (en) | 2010-06-10 | 2011-12-15 | Coatex S.A.S. | Hydroxy polyalkylene glycol function (meth) acrylic comb polymers, their use as shear-thinning agents in coating dispersions and dispersions containing them |
EP2777934A1 (fr) | 2011-11-10 | 2014-09-17 | Nippon Paper Industries Co., Ltd | Matériau d'emballage à papier barrière |
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