EP2898147A1 - Chlorofluoropolymer coated substrates and methods for producing the same - Google Patents
Chlorofluoropolymer coated substrates and methods for producing the sameInfo
- Publication number
- EP2898147A1 EP2898147A1 EP13839104.0A EP13839104A EP2898147A1 EP 2898147 A1 EP2898147 A1 EP 2898147A1 EP 13839104 A EP13839104 A EP 13839104A EP 2898147 A1 EP2898147 A1 EP 2898147A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- olefin
- coated substrate
- copolymer
- vinylester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
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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
- D21H19/10—Coatings without pigments
-
- 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
- D21H19/12—Coatings without pigments applied as a solution using water as the only solvent, e.g. in the presence of acid or alkaline compounds
-
- 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
- D21H19/20—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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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
- 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
- D21H21/14—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 function or properties in or on the paper
- D21H21/16—Sizing or water-repelling agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
Definitions
- the present disclosure relates to aqueous chlorofluoropolymer dispersions used in substrate coating applications.
- the present disclosure relates to aqueous chlorofluoropolymer dispersions applied to cellulosic fiber substrates.
- paper based products as packaging materials to pack, for example, food, alcoholic beverages, perfumes and cosmetics, medical and tobacco products, among others, is growing due to their bio-degradability and sustainability.
- Paper products lack chemical, solvent, oil, and stain resistance, moisture and aroma-barrier, and heat sealability properties.
- laminating paper products with PVC imparts barrier and heat sealability properties to paper, they do not have chemical, solvent, oil and stain resistance.
- a coated substrate which includes a substrate including a cellulosic fiber material and a copolymer coated in a thin film on at least one surface of the substrate.
- the copolymer has at least two comonomer units of the formula: CX 2 CYA, wherein C is carbon and wherein each X is independently selected from the group consisting of H, CI and F; Y is selected from the group consisting of H, CI, F, 0(CZ 2 ) n CZ 3 , (CZ 2 ) n CZ 3 , (OCZ 2 CZ 2 ) n CZ 3 and (0(CZ 2 ) n ) n CZ 3 , wherein each n is independently from about 1 to about 12 and each Z is independently selected from the group consisting of H, CI and F; and A is selected from the group consisting of H, CI and F; provided that for at least one comonomer unit, at least one of A, Y,
- a method of coating a substrate which includes the step of contacting at least one surface of a substrate including a cellulosic fiber material with an aqueous dispersion of a copolymer.
- the copolymer has at least two comonomer units of the formula: CX 2 CYA, wherein each X is independently selected from the group consisting of H, CI and F; Y is selected from the group consisting of H, CI, F, 0(CZ 2 ) n CZ 3 , (CZ 2 ) n CZ 3 , (OCZ 2 CZ 2 ) n CZ 3 and (0(CZ 2 ) n ) n CZ 3 , wherein each n is independently from about 1 to about 12 and each Z is independently selected from the group consisting of H, CI and F; and A is selected from the group consisting of H, CI and F; provided that for at least one comonomer unit, at least one of A,
- Embodiments of the present disclosure are broadly directed to the application of chlorofluoro-olefin/fluoro-olefin copolymers to cellulosic fiber substrates.
- cellulosic fiber substrates can include what will hereinafter be referred to as "paper” or “paper products.”
- paper and paper products are intended to broadly and inclusively refer to the class of substrates that is derived from cellulosic fiber pulp and is provided in the form of dried sheets, paper or card boards of cellulosic fibers.
- An exemplary method for producing "paper” or “paper products” as used herein is briefly set forth below, by way of a non-limiting example.
- coatings in accordance with the present disclosure may be applied to the wood product itself (i.e., a hard wood product that has not been processed into pulp).
- wood products serve as suitable substrates for the application coatings described herein as well.
- Cellulosic pulp is generally described in relation to cellulosic fibers derived from wood pulp. However, the embodiments described herein may be used in conjunction with any cellulosic fiber derived from any source.
- Exemplary cellulosic fibers include, but are not limited to, those derived from wood, such as wood pulp, as well as non-woody fibers from cotton, from straws and grasses, such as rice and esparto, from canes and reeds, such as bagasse, from bamboos, from stalks with bast fibers, such as jute, flax, kenaf, cannabis, linen and ramie, and from leaf fibers, such as abaca and sisal. It is also possible to use mixtures of one or more cellulosic fibers.
- Wood fibers suitable for use in the described embodiments may be derived from either a softwood pulp source or hardwood pulp source or mixtures thereof.
- exemplary softwood pulp sources include trees such as various pines (Slash pine, Loblolly pine, White pine, Caribbean pine), Western hemlock, various spruces, (e.g., Sitka Spruce), Douglas fir and/or mixtures of same.
- exemplary hardwood pulp sources include trees such as sweet gum, black gum, maple, oak, eucalyptus, poplar, beech, and aspen or mixtures thereof.
- the term "pulp” simply refers to a mass or agglomeration of cellulose fibers.
- the pulp may be supplied in a dry form or as slurry.
- the term “fiber” or “fibrous” is meant to refer to a particulate material wherein the length to diameter ratio of such particulate material is greater than about 10.
- the cellulosic fibers are characterized by an average length, e.g., a WAFL length, between about 0.1 to 6 mm. In other embodiments, the average fiber length is between about 0.8 and 4 mm.
- Cellulose pulp is produced using a primary pulping process as known in the art.
- Exemplary wood pulping operations generally entail a series of steps, such as digestion, deknotting and the like, that separate the pulp into individual fibers and remove impurities from the pulp.
- An exemplary wood pulping operation is the Kraft pulping process, as is known in the art.
- chemical pulping operations such as, but not limited to, sulfite pulping operations, and organic solvent pulping operations, may also be used.
- paper based products as packaging materials to pack, for example, food, alcoholic beverages, perfumes and cosmetics, medical and tobacco products, among others, is growing due to their bio-degradability and sustainability.
- Paper products lack chemical, solvent and oil resistance, moisture and aroma-barrier, and heat sealability properties.
- laminating paper products with PVC imparts barrier and heat sealability properties to paper, they do not have chemical and solvent resistance.
- chlorofluoro-olefin/fluoro-olefin copolymers impart desirable chemical, and solvent and oil resistance when applied to paper based products, in addition to the moisture-barrier and heat sealability properties that were previously known with regard to PVC coatings.
- Chlorofluoro-olefin/fluoro-olefin copolymers are found to have many inherent advantages. Chlorofluoro-olefin/fluoro-olefin copolymers are abrasion resistant and when formed into a film have >90% solar light transmission. Chlorofluoro-olefin/fluoro-olefin copolymers have many fabricating advantages over PTFE, polytetrafluoroethylene- hexafluoropropylene copolymers (FEP) and polytetrafluoroethylene-hexafluoropropylene- vinylidenefluoride (THV, manufactured by Dyneon) terpolymers.
- FEP polytetrafluoroethylene- hexafluoropropylene copolymers
- TSV polytetrafluoroethylene-hexafluoropropylene- vinylidenefluoride
- Chlorofluoro-olefin/fluoro- olefin copolymers can be processed at mild, ambient temperatures and can be easily recoated by successive coatings of aqueous chlorofluoro-olefin/fluoro-olefm copolymer dispersions.
- chlorofluoro-olefin/fluoro-olefin copolymers have a relatively high surface tension, recoating with successive passes of these copolymers can be accomplished with very low levels of wetting agents, 0.1-2 weight % being typical depending on whether the wetting agent additive is fluorinated, perfluorinated, or non-fluorinated, or any mixture thereof.
- Chlorofluoro- olefin/fluoro-olefin copolymers are excellent film formers that facilitate the production of dispersion cast film for lamination onto fabric, or the direct coating/recoating of fabric to a desired thickness with low levels of wetting agents. Further, chlorofluoro-olefin/fluoro-olefin coatings resist solvents, acids, oils, stains, abrasion and UV and many other environmental impacts.
- chlorofluoro-olefm copolymers are capable of forming aqueous chlorofluoro-olefin copolymer dispersions, and as such are particularly suitable for use in the application thereof to paper and paper products as the paper and paper products can simply be immersed in the dispersion for a period time, and then dried.
- aqueous chlorofluoro- olefin copolymer dispersions can be prepared from ultrahigh molecular weight chlorofluoro- olefin copolymers that could not be otherwise formed by melt extrusion. When coalescing emulsion particles, entanglement of the chain ends between polymer particles is only needed, not a melt flow of the bulk.
- the minimum film formation temperature is the primary factor determining film formation.
- Coalescence is independent of polymer melt viscosity and polymer molecular weight.
- the high molecular weight of the chlorofluoro-olefin copolymers restricts the polymer chain mobility and limits UV- induced crystallization that would otherwise cause the formation of large, brittle spherulites, and any other morphological changes. It is also believed that the high molecular weight decreases the copolymer's tendency to move or deform permanently under the influence of stresses. Other benefits of the high polymer molecular weight include improved solvent resistance and increased toughness. In particular, the copolymers have a higher modulus and tensile strength and are more abrasion resistant.
- CTFE is available from Honeywell International Inc. of Morristown, NJ
- VDF is available from Solvay S.A. of Brussels, Belgium
- vinyl esters are from The Dow Chemical Company of Midland, MI.
- At least one comonomer from which the copolymer composition is prepared is a chlorofiuoro-olefin.
- Suitable chlorofluoro-olefins include polychlorinated fluoroolefins such as CTFE,
- fluorotrichloroethylene 1,1-dichlorodifluoroethylene, cis and trans isomers of 1,2- dichlorodifluoroethylene, 1-chloro-l-fluoroethylene, perchlorofluoroethers and
- Copolymer compositions may be prepared from up to three different chlorofiuoro-olefin comonomers.
- one or two chlorofiuoro-olefin comonomers may be copolymerized with one or two fluoro-olefins.
- Suitable fluoro-olefin comonomers from which the copolymer composition may be prepared have the formula CX 2 CYA, wherein X, Y and A each do not include CI but otherwise are as defined above.
- Preferred fluoro-olefin comonomers include partially and perfluorinated olefins such as VDF, TFE, HFP, vinylfluoride and 1,2- difluoroethylene, fluorinated alpha-olefms such as 3,3,4,4,4-penta-fluoro-l-butene,
- perfluoroethers such as perfluoro(propylvinylether) and perfluoro-dioxoles such as
- Exemplary copolymers contain predominantly chlorotrifluoroethylene, and at least one fluoro-olefin selected from the group: VDF, hexafluoropropylene, tetrafluoroethylene, vinylfluoride, trifluoroethylene, and fluorinated or perfluorinated alkylvinylethers such as perfluoropropyl vinylether.
- the comonomers used to make the copolymer composition are selected from CTFE, VDF and a fluorinated vinyl ester.
- the comonomers may have the formula CX 2 CYA, wherein X, Y and A are as defined above, excluding olefins in which each X and A are hydrogen, provided that at least one comonomer unit contains a chlorine atom.
- the comonomers used to make the copolymer composition are CTFE and VDF.
- the copolymer compositions may optionally include a chloro-olefin comonomer.
- any chloro-olefin may be employed, and among the suitable chloro-olefins are vinylidene chloride, vinyl chloride and trichloroethylene.
- the copolymer compositions may also optionally include a non-halogenated vinyl ester or an acid as a comonomer in addition to the halogenated olefins, provided that at least two halogenated olefin comonomers are employed.
- the vinyl ester is preferably an alkyl vinylester, in which the alkyl group contains from about 1 to about 12 carbon atoms.
- the acid comonomers include acrylic acid, methacrylic acid, methyl methacrylate and other alkyl acrylates. Both vinyl ester and acid comonomers are all commercially available from, for instance, The Dow Chemical Company of Midland, MI.
- Preferred vinyl esters include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl isobutyrate, vinyl hexanoate, vinyl stearate, neononanoate ethenyl ester, vinyl esters of n-valeric, caproic, lauric, versatic, isovaleric, 2-ethyl hexanoic, 2,2-dimethyl octanoic, 2-methyl-2 -propyl pentanoic and 4-methyl-4-butyl hexanoic acids, as well as neoacid vinylesters.
- Preferred acids include acrylic and methacrylic acids.
- vinyl propionate and vinyl butyrate serve as suitable non-limiting examples.
- Vinyl propionate is a partially water- soluble olefin which accelerates the emulsion polymerization of chlorofluoro-olefins and fluoro- olefins. Because of the slightly branched nature of vinyl propionate, it also slows crystallization and the formation of large spherulites, while not preventing their formation.
- Non-halogenated olefins such as ethylene or propylene can also be incorporated into the polymer.
- each monomeric unit used to prepare the copolymer will mostly depend on the application in which the material will be used (e.g., a room temperature application generally requires a composition with a glass transition temperature close to room temperature).
- a room temperature application generally requires a composition with a glass transition temperature close to room temperature.
- increasing levels of comonomer leads to decreasing glass transition temperatures.
- One skilled in the art can readily and without undue experimentation optimize these ranges to obtain an essentially amorphous chlorofluoropolymer composition having the desired properties.
- Exemplary polymers contain less than about 90 weight % of a chlorofluoro-olefin, up to about 30 weight % of a fluoro-olefin, and from about 0 to about 10 weight % of a vinylester and/or a non-fluorinated olefin.
- comonomers used to make the copolymer contain less than about 90 weight % of a chlorofluoro-olefin, up to about 30 weight % of a fluoro-olefin, and from about 0 to about 10 weight % of a vinylester and/or a non-fluorinated olefin.
- the CTFE is present in an amount of from about 70 to about 95 weight %, for example from about 75 to about 94 weight %, and such as from about 80 to about 90 weight %.
- the comonomers used to prepare the copolymer composition are CTFE, VDF and a vinylester
- the vinylester is present in an amount of from about 0.1 to about 5 weight %, for example from about 0.5 to about 3 weight %
- the VDF component is present in an amount of from about 5 to about 25 weight %, for example from about 10 to about 25 weight %
- the CTFE component is present in an amount less than about 88 weight %, for example less than about 85 weight %.
- copolymers of the invention have a crystallinity index from 0 to about 10%.
- Polymers having a crystallinity index of no greater than 5% are most preferred.
- weight-average molecular weights between about 2,000,000 and about 20,000,000 Daltons are suitable. Weight-average molecular weights less than 10,000,000 Daltons are typical, with a weight-average molecular weight of about 8,000,000 Daltons being particularly suitable.
- copolymers suitable for use in accordance with the present disclosure are:
- radical initiator Any commercially available radical initiator may be used in accordance with the embodiments described herein. Suitable candidates include thermal initiators and oxidation-reduction or "redox" initiator systems.
- Thermal initiators include: metal persulfates like potassium persulfate and ammonium persulfate; organic peroxides or hydroperoxides such as diacyl peroxides, ketone peroxides, peroxyesters, dialkyl peroxides and peroxy ketals; azo initiators such as 2,2'-azobisisobutyronitrile and water- soluble analogues thereof; and mixtures of any of the foregoing.
- Any redox initiator system known to be useful in the preparation of fluoropolymers such as PCTFE may be used in the present invention.
- Exemplary redox initiator systems include: 1) an organic or inorganic oxidizing agent or mixtures thereof; and 2) an organic or inorganic reducing agent or mixtures thereof.
- Suitable oxidizing agents include metal persulfates such as potassium persulfate and ammonium persulfate; peroxides such as hydrogen peroxide, potassium peroxide, ammonium peroxide, tertiary butyl hydroperoxide (“TBHP”) ((CH 3 ) 3 COOH), cumene hydroperoxide, and t-amyl hydroperoxide; manganese triacetate; potassium permanganate;
- Suitable reducing agents include sodium sulfites such as sodium bisulfite, sodium sulfite, sodium pyrosulfite, sodium-m-bisulfite ("MBS") (Na 2 S 2 0 5 ) and sodium thiosulfate; other sulfites such as ammonium bisulfite; hydroxylamine; hydrazine;
- ferrous irons organic acids such as oxalic acid, malonic acid, citric acid and mixtures thereof.
- a suitable free radical initiating system is one that serves to simultaneously emulsify the polymer while initiating the polymerization, thus eliminating the need for large quantities of surfactants.
- Redox initiator systems are suitable for this purpose.
- Exemplary redox initiator systems use an MBS reducing agent and a TBHP oxidizing agent.
- the redox initiator system is used in conjunction with a transition metal accelerator. Accelerators can greatly reduce the polymerization time.
- Any commercially available transition metal may be used as an accelerator in the invention.
- Exemplary transition metals include copper, silver, titanium, ferrous iron and mixtures thereof.
- the amount of radical initiator used in the process depends on the relative ease with which the various monomers copolymerize, the molecular weight of the polymer and the rate of reaction desired. Generally, from about 10 to about 100,000 ppm of initiator may be used, for example from about 100 to about 10,000 ppm.
- the redox initiator system may include additional peroxide-based compounds.
- the amount of additional peroxide-based compound used ranges from about 10 to about 10,000 ppm, for example from about 100 to about 5,000 ppm.
- the radical initiator may be added before, simultaneous with and/or shortly after the addition and/or consumption of the monomers used to make the copolymer.
- an additional peroxide-based compound when used it may be added at the same interval specified for the primary radical initiator.
- the chlorofluoropolymer compositions of the present disclosure may be made by a two-step polymerization reaction.
- monomers, water, and an initial charge of radical initiator are introduced into suitable polymerization vessel. Additional monomer is added throughout the reaction at a rate equal to the rate of consumption to maintain a constant pressure. Incremental additional charges of initiator are introduced into the vessel over the duration of the reaction to sustain the polymerization.
- the reaction mixture is maintained at a controlled temperature while all reactants are being charged to the vessel and throughout the polymerization reaction.
- reaction vessel used to prepare the composition described herein is that it be capable of being pressurized and agitated.
- Conventional commercial autoclaves which can be sealed and pressurized to the required reaction pressures (preferably in excess of 3.36 MPa (500 psig)) are preferred.
- Horizontally inclined autoclaves are preferred to vertically inclined autoclaves, although both geometries can be used.
- the aqueous medium in which the polymerization is conducted is deionized, nitrogen- purged water. Generally, an amount equivalent to approximately half the capacity of the vessel, such as an autoclave, is used.
- the ratio of polymer to water is chosen in such a way to obtain a dispersion of about 20 to about 60% polymer solids in water.
- the water is pre-charged to the autoclave.
- the process is a surfactant-free emulsion polymerization process that does not require a separate post-concentration step to obtain high levels of emulsified polymer in water.
- the monomers may be charged to the reactor vessel either in a semicontinuous or a continuous manner during the course of the polymerization.
- "Semicontinuous,” as used herein, means that a number of batches of the monomers are charged to the reactor during the course of the polymerization reaction.
- the batch size is determined by the desired operating pressure.
- the molar ratio of total monomer consumed to radical initiator will depend upon the overall particle size and molecular weight desired. In an embodiment, the overall mole ratio of monomer to initiator would be from about 10 to about 10,000, for example from about 50 to about 1,000, and such as from about 100 to about 500 moles of total monomer to one mole of initiator.
- the radical initiator is generally added incrementally over the course of the reaction.
- initial charge or “initial charging” of initiator refers to a rapid, large, single or incremental addition of initiator to effect the onset of polymerization.
- initial charge generally between about 10 ppm/min to about 1,000 ppm/min is added over a period of from about 3 to about 30 minutes, either before, after, or during the charging of the monomers.
- continuous charge or “continuous charging” means the slow, small, incremental addition of initiator over a period of from about 1 hour to about 6 hours, or until polymerization has concluded.
- in the continuous charge generally between about 0.1 ppm/min to about 30 ppm/min of initiator is added.
- the sealed reactor and its contents are maintained at the desired reaction temperature, or alternately to a varying temperature profile which varies the temperature during the course of the reaction.
- Control of the reaction temperature is a factor for establishing the final molecular weight of the chlorofluoropolymers produced.
- polymerization temperature is inversely proportional to product molecular weight.
- the reaction temperature should range between about 0°C to about 120°C, although temperatures above and below these values are also contemplated.
- the reaction pressure is between from about 172 KPa to about 5.5 MPa, and for example from about 345 KPa to about 4.2 MPa. Elevated pressures and temperatures will yield greater reaction rates.
- the polymerization is conducted under agitation to ensure proper mixing.
- An adjustment of the agitation rate during the polymerization may be desirable to prevent premature coagulation of the particles.
- the agitation rate and reaction time will typically depend upon the amount of chlorofluoropolymer product desired, one of ordinary skill in the art can readily optimize the conditions of the reaction without undue experimentation to get the claimed results.
- the agitation rate will generally be in the range of from about 5 to about 800 rpm and, for example from about 25 to about 700 rpm, depending on the geometry of the agitator and the size of the vessel.
- the reaction time will generally range from about 1 to about 24 hours, for example from about 1 to about 8 hours.
- the chlorofluoropolymers produced using the above surfactant- free process are self- emulsifiable chlorofluorinated macromolecules having inorganic, "surfactant-like" functional end groups that impart excellent latex stability to the polymer when present in very low concentration.
- the chlorofluoropolymers produced are thereby dispersed in the aqueous medium by the attachment of these inorganic fragments onto the end of the polymer repeating units, thus creating a surface active agent having both a hydrophobic component and a hydrophilic component. This attachment leads to micelle formation, or, if the concentration of functionalized end groups is high enough, to their complete dissolution in water.
- the type of "surfactant-like" end groups produced depends upon the type of initiator system selected and the optional addition of compounds that might be incorporated into the polymer through chain transfer reactions.
- emulsifying functional end groups include, but are not limited to, sulfonates, carboxylates, phosphonates, phosphates and salts and acids thereof, ammonium salts and any mixture thereof.
- the presence of sulfonic acid end groups has been discovered to most significantly affect the emulsification of the chlorofluoropolymers in water.
- the amount of these functional end groups in the dispersion can be determined by first purifying the dispersion by methods known to the art, such as by ion exchange or dialysis, titrating the dispersion with any known base such as aqueous sodium hydroxide or ammonium hydroxide, and then expressing the amount in terms of molar equivalents of titrated base.
- the amount of these functional end groups expressed in moles of equivalent NaOH may range between from about 0.0001 to about 0.5 moles of functional end groups per liter of chlorofluoropolymer dispersion obtained.
- the molar ratio of these functional end groups per fluoropolymer produced may range from about 1 : 10 to 10,000, for example from about 1 :10 to 1,000, such as from about 1 :50 to 500.
- An exemplary chlorofluoropolymer dispersion within the scope of this disclosure contains about 0.01 molar equivalents/kg of dry polymer.
- the resulting particle size distribution of the dispersion produced according to the process of the invention will be monodisperse and narrow.
- “Monodisperse distribution” as used herein means a single distribution of particle sizes.
- the particle distribution ranges between about 0.1 microns and about 0.4 microns, and for example from about 0.1 to about 0.3 microns.
- the dispersions as described herein are prepared using a surfactant- free emulsion process to obtain stable dispersions having up to 45 weight % solids in water, which are obtained without a concentration step.
- Low levels of surfactants are added if further particle size control is desired, or to obtain higher levels of emulsified polymer in water (i.e., 40-60 weight %).
- Any commercially available surfactant may optionally be pre-charged or added batch-wise during or subsequent to the onset of polymerization to further manipulate particle size, particle number and particle distribution. It is well known in the art that the addition of more surfactant during the course of polymerization to emulsions already containing surfactants sometimes creates new particles and thus produces a bimodal distribution of particles or a broad distribution of particles.
- Suitable surfactants will readily occur to those skilled in the art and include anionic, cationic and nonionic surfactants.
- An exemplary dispersion is an anionic surfactant stabilized latex emulsion having from 0 to 0.25 weight % of an anionic emulsifier.
- suitable perfluorinated anionic surfactants include perfluorinated ammonium octanoate, perfluorinated alkyl/aryl ammonium (metal) carboxylates and perfluorinated alkyl/aryl lithium (metal) sulfonates wherein the alkyl group has from about 1 to about 20 carbon atoms.
- Suitable surfactants also include fluorinated ionic or nonionic surfactants, hydrocarbon-based surfactants such as the alkylbenzenesulfonates or mixtures of any of the foregoing.
- the chlorofluoropolymers produced by the process of the invention may be isolated by conventional methods such as evaporating the water medium, freeze-drying the aqueous suspension, or adding a minor amount of an agglomerating or coagulating agent such as ammonium carbonate, followed by filtration or centrifuging. Alternatively and preferably the chlorofiuoropolymer dispersion produced is used as is.
- dispersions of chlorofluoro- olefin/fluoro-olefin copolymers as described in the present disclosure and the vinylester terpolymers thereof can be coated at temperatures lower than 120°C onto paper and paper products.
- Non-limiting examples of industrial uses for such paper and paper products include packaging food, alcoholic beverages, perfumes and cosmetics, medical and tobacco products, In particular, the coated paper imparted with moisture barrier property will be useful as a lid foil for blister packs in pharmaceutical packaging.
- chlorofluoro-olefin/fluoro-olefin copolymers are coated on a paper or paper product substrate in multi-pass processes, although a single-pass process may also be used.
- the paper product may be immersed in the above-described aqueous dispersions of chlorofluoro-olefin/fluoro-olefin copolymers for a period of time ranging between about 60 seconds to 1 hour.
- the application process is able to occur at ambient temperatures, for example from about 20 - 30°C. Thereafter, the paper product may be removed from the aqueous dispersion, and allowed to dry. Drying may be performed at an elevated temperature to increase the speed at which the paper product dries, for example from about 70 - 120 C in an oven. The drying process may also be expedited with air or nitrogen Thereafter, the application process can be repeated any number of times to produce the desired thickness of coating on the paper product, for example one, two, three, four, five, or more times.
- the resulting coated paper or paper product desirably is hydrophobic, and does not allow solvent such as isopropyl alcohol ("IPA"), toluene, or ethanol, for example, to penetrate through the paper.
- IPA isopropyl alcohol
- the coated paper also does not allow oil or grease to penetrate through the paper and resistant to stain.
- the coated paper seals itself upon heating and the sealed paper maintains its properties.
- the coated paper further provides a barrier to moisture and aroma, and the moisture and aroma-barrier property can be tailored by adjusting the thickness and kind (for example, one-sided or two-sided) of coating.
- CTFE/VDF/Vinyl propionate terpolymer dispersion was prepared having 80.1 weight % chlorotrifluoroethylene, 16.5 weight % vinylidenefluoride and 3.4 weight % vinyl propionate.
- a 3 Gallon glass-lined autoclave was first filled with 1.57 gallons of deionized water and then nitrogen sparged to remove oxygen. The autoclave was then filled with 585 g of CTFE and 116 grams of VDF and heated to 19 ° C (66.2 ° F). 5.7 G of 70% solution of tertiary butyl hydroperoxide (TBHP) in water was further diluted to 35.7 mL with deionized water.
- TBHP tertiary butyl hydroperoxide
- Example 2 To the dispersion obtained in Example 1 was added 2.0 weight % (based on the weight of dispersion) of Capstone FS-32 fluorosurfactant (from Du Pont) and mixed thoroughly. The mixture was then coated onto a laminated paper (from Coldenhove, Netherlands) at room temperature using multiple passes to achieve a thickness of 1.5 mils coating on each side of the paper. Total thickness of the coated paper corresponds to 4.9 mils. The coated paper was dried in an air oven at 80 °C between coats. The coated paper was then subjected to MOCON testing at 40 °C and 70% relative humidity to give a water vapor transmission rate of 0.0929 grams/ lOOin 2 -day. Upon heating the coated paper to 175 °C ( ⁇ 350 °F), it heat seals itself and the attempts to break the seal results the paper getting ripped indicating the seal is intact
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201261704956P | 2012-09-24 | 2012-09-24 | |
US13/834,800 US20140087195A1 (en) | 2012-09-24 | 2013-03-15 | Chlorofluoropolymer coated substrates and methods for producing the same |
PCT/US2013/059383 WO2014046954A1 (en) | 2012-09-24 | 2013-09-12 | Chlorofluoropolymer coated substrates and methods for producing the same |
Publications (3)
Publication Number | Publication Date |
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EP2898147A1 true EP2898147A1 (en) | 2015-07-29 |
EP2898147A4 EP2898147A4 (en) | 2016-05-04 |
EP2898147B1 EP2898147B1 (en) | 2020-06-10 |
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EP13839104.0A Active EP2898147B1 (en) | 2012-09-24 | 2013-09-12 | Chlorofluoropolymer coated substrates and methods for producing the same |
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US (1) | US20140087195A1 (en) |
EP (1) | EP2898147B1 (en) |
JP (1) | JP6348496B2 (en) |
KR (1) | KR102257643B1 (en) |
CN (1) | CN104641040A (en) |
BR (1) | BR112015006244A2 (en) |
CA (1) | CA2884590C (en) |
MX (1) | MX2015003521A (en) |
WO (1) | WO2014046954A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN105829367A (en) | 2013-10-22 | 2016-08-03 | 霍尼韦尔国际公司 | Curable fluorocopolymer formed from tetrafluoropropene |
US10435580B2 (en) | 2015-11-20 | 2019-10-08 | Honeywell International Inc. | Gloss retentive fluorocopolymers for coating applications |
US20190002656A1 (en) * | 2015-08-26 | 2019-01-03 | Bemis Company, Inc. | Anti-Scalping Pharmaceutical Packaging Film |
US11015005B2 (en) | 2015-11-20 | 2021-05-25 | Honeywell International Inc. | Fluorocopolymers for coating applications |
JP6683884B2 (en) * | 2016-07-27 | 2020-04-22 | ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. | Film layer and method of forming the same |
CN110869400A (en) * | 2017-05-12 | 2020-03-06 | 霍尼韦尔国际公司 | Copolymers and terpolymers based on chlorotrifluoroethylene and vinyl chloride and use thereof |
KR102328470B1 (en) * | 2017-05-12 | 2021-11-18 | 허니웰 인터내셔날 인코포레이티드 | Copolymers and trimers based on chlorotrifluoroethylene and vinyl chloride and their uses |
KR102512161B1 (en) * | 2022-05-02 | 2023-03-22 | (주)미지건설 | Construction method for repairing concrete structure using quick-hardening cement mortar composition and surface protection coating agent for self-healing and crack-reducing type repairs |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3531441A (en) * | 1966-03-01 | 1970-09-29 | Du Pont | Interpolymers of vinyl fluoride |
US3449305A (en) * | 1966-03-01 | 1969-06-10 | Du Pont | Interpolymers of vinylidene fluoride |
US3839144A (en) * | 1970-09-21 | 1974-10-01 | W Lounden | Paper having 60{14 97 percent hydrated cellulosic fibers and 3{14 40 percent unhydrated cellulosic fibers |
JPS6067517A (en) * | 1983-09-21 | 1985-04-17 | Daikin Ind Ltd | Fluorine-contained copolymer |
US4581412A (en) * | 1983-09-21 | 1986-04-08 | Daikin Kogyo Co., Ltd. | Coating composition of vinylidene fluoride copolymer and acrylic polymer |
JPS61261367A (en) * | 1985-05-15 | 1986-11-19 | Dainippon Ink & Chem Inc | Emulsion paint composition |
DE3688000T2 (en) * | 1985-05-16 | 1993-10-21 | Chemfab Corp | Flexible composite laminates containing a fluoropolymer. |
GB8713362D0 (en) * | 1987-06-08 | 1987-07-15 | Ici Plc | Fluorocopolymer compositions |
US4808467A (en) * | 1987-09-15 | 1989-02-28 | James River Corporation Of Virginia | High strength hydroentangled nonwoven fabric |
JP3087286B2 (en) * | 1990-05-22 | 2000-09-11 | ダイキン工業株式会社 | Vinylidene fluoride copolymer and curing composition containing it |
US5776842A (en) * | 1994-06-23 | 1998-07-07 | Cellresin Technologies, Llc | Cellulosic web with a contaminant barrier or trap |
FR2737228B1 (en) * | 1995-07-24 | 1997-09-05 | Sibille Dalle | COATED SULFURIZED PAPER AND MANUFACTURING METHOD THEREOF |
US5612416A (en) * | 1995-10-10 | 1997-03-18 | Ppg Industries, Inc. | Unsaturated hydroxy diester copolymers and their use in coating compositions |
US6369178B1 (en) | 1998-12-23 | 2002-04-09 | Alliedsignal Inc. | Poly (chlorotrifluoroethylene/vinylidenefluoride/vinylester) copolymers with excellent long-term ultraviolet light resistance |
US6494328B1 (en) * | 2000-08-23 | 2002-12-17 | L&P Property Management Company | Modular gravity feed dispenser unit |
AU2003235863A1 (en) * | 2002-05-10 | 2003-11-11 | Daikin Industries, Ltd. | Surfactant and dispersion aid each comprising graft fluoropolymer |
CA2703595A1 (en) * | 2010-05-12 | 2011-11-12 | Rajan Ahluwalia | Process for producing recycled paper |
-
2013
- 2013-03-15 US US13/834,800 patent/US20140087195A1/en not_active Abandoned
- 2013-09-12 EP EP13839104.0A patent/EP2898147B1/en active Active
- 2013-09-12 MX MX2015003521A patent/MX2015003521A/en active IP Right Grant
- 2013-09-12 JP JP2015533113A patent/JP6348496B2/en active Active
- 2013-09-12 CN CN201380049396.2A patent/CN104641040A/en active Pending
- 2013-09-12 BR BR112015006244A patent/BR112015006244A2/en not_active IP Right Cessation
- 2013-09-12 KR KR1020157006947A patent/KR102257643B1/en active IP Right Grant
- 2013-09-12 WO PCT/US2013/059383 patent/WO2014046954A1/en active Application Filing
- 2013-09-12 CA CA2884590A patent/CA2884590C/en active Active
Also Published As
Publication number | Publication date |
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EP2898147B1 (en) | 2020-06-10 |
US20140087195A1 (en) | 2014-03-27 |
CA2884590C (en) | 2021-08-24 |
JP2015530495A (en) | 2015-10-15 |
KR20150058235A (en) | 2015-05-28 |
JP6348496B2 (en) | 2018-06-27 |
WO2014046954A1 (en) | 2014-03-27 |
CA2884590A1 (en) | 2014-03-27 |
EP2898147A4 (en) | 2016-05-04 |
MX2015003521A (en) | 2015-07-17 |
KR102257643B1 (en) | 2021-06-01 |
CN104641040A (en) | 2015-05-20 |
BR112015006244A2 (en) | 2017-07-04 |
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