EP1919694A1 - Method and apparatus for continuously preparing crosslinked, solution-cast polymer film - Google Patents
Method and apparatus for continuously preparing crosslinked, solution-cast polymer filmInfo
- Publication number
- EP1919694A1 EP1919694A1 EP06836237A EP06836237A EP1919694A1 EP 1919694 A1 EP1919694 A1 EP 1919694A1 EP 06836237 A EP06836237 A EP 06836237A EP 06836237 A EP06836237 A EP 06836237A EP 1919694 A1 EP1919694 A1 EP 1919694A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polymer solution
- crosslinking agent
- continuously
- polymer
- casting
- 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.)
- Withdrawn
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/14—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor for making articles of indefinite length
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/205—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
- C08J3/21—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
- C08J3/215—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase at least one additive being also premixed with a liquid phase
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2029/00—Use of polyvinylalcohols, polyvinylethers, polyvinylaldehydes, polyvinylketones or polyvinylketals or derivatives thereof as moulding material
- B29K2029/04—PVOH, i.e. polyvinyl alcohol
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2329/00—Characterised by the use 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 alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
- C08J2329/02—Homopolymers or copolymers of unsaturated alcohols
- C08J2329/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
Definitions
- the disclosure relates generally to a method and apparatus for continuous solution casting of a polymer to create a film. More particularly, the disclosure relates to a method and apparatus for injecting a secondary agent, such as a cross.-linking agent, into a stream of polymer solution just upstream of a casting die, for continuously producing a polymer film, such as polyvinyl alcohol, that is crosslinked.
- a secondary agent such as a cross.-linking agent
- Typical solvent casting systems utilize an organic solvent such as acetone, aniline, dimethyl sulfoxide (DMSO), benzene, dimethyl formamide (DMF), methyl Atty. Docket No.30658/40658A PATENT APPLICATION
- Extrusion and calendering are processes which melt the polymer and shape the plastic prior to freezing.
- Plastisol and organosol casting processes involve the melting of the polymer in a plasticizer matrix, after which the solvent action of the plasticizer forms a film.
- the solution that is eventually cast onto a moving surface containing the base polymer and secondary components such as plasticizers, fillers, surfactants, actives, and colorants, is prepared by combining the base polymer and secondary components with water in a tank and then mixing.
- the homogeneous solution or suspension is then pumped through one or more operations including de-aeration and filtering and then fed to a solution casting die for casting onto the moving surface, such as a traveling belt.
- PVOH Polyvinyl alcohol
- One aspect of the disclosure provides a method for continuously preparing a solvent cast film having a secondary component, including continuously providing a pressurized stream of polymer solution, combining a fluid stream including a crosslinking agent with the pressurized stream of polymer solution, mixing the combination of polymer solution and fluid stream in-line, continuously applying the resulting homogeneous mixture of polymer solution and crosslinking agent to a moving surface, and then evaporating solvent from the mixture.
- Another aspect of the disclosure provides an improved method of casting a polymer solution including a crosslinking agent onto a substrate for evaporating off a solvent and forming a crosslinked film, the improvement including continuously injecting the crosslinking agent into a stream of polymer solution, mixing the resulting stream of polymer solution with the crosslinking agent in-line, and then casting the resulting polymer solution onto a moving substrate to continuously produce crosslinked film.
- Figure 1 shows and example of a system for solvent casting according to the disclosure
- Figure 2 shows an embodiment of an adjustable sheeting die for casting polymer solution
- Figure 3 shows an example of the relationship between drums and a band in a basic band casting machine
- Figures 4 (elevation view) and 5 (plan view) show an embodiment of an injection system and associated feed and in-line mixing components.
- the invention generally relates to a method and apparatus for solution casting to continuously form a polymer film that includes one or more secondary components.
- the solution cast process offers several unique features which conventional fusion processes lack.
- film formation depends upon solubility, not melting.
- a wide range of polymeric alloys can be produced by solvent casting. Because the flowability to form a film is provided by the solvent, a pure resin firm can be manufactured without adulteration by heat, stabilizers, plasticizers, or lubricants. Only additives which are beneficial to the finished product need to be incorporated with the polymer.
- Solvent casting can provide a firm which has excellent dimensional stability as well as reduction in or freedom from pinholes, gels and other imperfections. Due to the very low heat history which is inherent in a film produced by solvent casting processing, the process can also provide an extended service life to the film.
- the method generally involves the steps of continuously pumping a feed of polymer solution towards a casting surface, continuously combining one or more secondary components with the feed of polymer solution, mixing the combination, and then depositing the combined solution onto the casting surface.
- the secondary component includes a crosslinking agent.
- the method involves continuously providing a pressurized stream of polymer solution, continuously combining a fluid stream including a secondary component with the pressurized feed of polymer solution, homogeneously mixing the combination of polymer solution and fluid stream in-line, continuously applying the resulting homogeneous mixture of polymer solution and secondary component to a continuously moving surface, and then evaporating solvent from the mixture to form a polymeric film.
- the secondary component includes a crosslinking agent
- the crosslinking begins upon introduction of the crosslinking agent into the polymer solution, and may continue after film formation and even after the product film is removed from the casting surface and collected (e.g., wound onto a roll).
- the polymer solution is any substantially homogeneous mixture of a polymer in a suitable solvent.
- polymer solution is used herein to refer to such a solution prior to continuous injection of a secondary component as described herein, except when stated otherwise.
- the disclosed method and system is ideally suited for a water-soluble polymer, such as polyvinyl alcohol (PVOH), dissolved in water.
- PVOH polyvinyl alcohol
- the water content of the PVOH solution is preferably within the range of from about 60% by weight to about 85% by weight.
- Suitable water-soluble materials include, but are not limited to polymers, copolymers and derivatives thereof.
- the water-soluble material can include a polymer selected from the following group, including water-soluble copolymers and other derivatives thereof, and mixtures thereof: polyvinyl alcohols, polyethylene oxides, dextrans, starches, cellulose derivatives (eg., hydroxyethyl cellulose, hydroxypropyl cellulose, and other cellulose ethers), polyvinylpyrrolidone, polyacrylamide, polyacrylic acid, polyacrylates, pectin, alginates, proteins and derivatized proteins (e.g., gelatin, corn zein, whey protein).
- a polymer selected from the following group including water-soluble copolymers and other derivatives thereof, and mixtures thereof: polyvinyl alcohols, polyethylene oxides, dextrans, starches, cellulose derivatives (eg., hydroxyethyl cellulose, hydroxypropyl cellulose, and other cellulose ethers), polyvinylpyrrolidone, polyacrylamide, polyacrylic acid, polyacrylates, pe
- PVOH polyvinyl alcohol
- a copolymer thereof is used, then the PVOH can be partially or fully hydrolyzed.
- Polyvinyl alcohol (PVOH) is a synthetic resin generally prepared by the alcoholysis, usually termed hydrolysis or saponification, of polyvinyl acetate.
- PVOH polymer If a sufficient number of acetate groups, are allowed to remain after the hydrolysis of polyvinyl acetate, the PVOH polymer then being known as partially hydrolyzed, it is more weakly hydrogen-bonded and less crystalline and is soluble in cold water — e.g., rapid dissolution at temperatures of about 10 °C and greater.
- the polymer solutions must be formulated in different ways. That is, a PVOH resin, crosslinking agent, plasticizer system and other ingredients can vary and can provide a range of films with different product characteristics, from a highly water-swellable hydrogel-type film to a rigid membrane film.
- Water soluble refers to a film which, when exposed to water, begins to dissolve or disintegrate to its smallest components.
- Polyvinyl alcohol (PVOH) is a hydrophilic polymer and the plasticizers typically used in its manufacture also have an affinity for water. PVOH will absorb moisture from a wet atmosphere and give up moisture to a dry atmosphere. As moisture content increases (even with humidity), a Atty. Docket No.30658/40658A PATENT APPLICATION
- PVOH film will tend to quickly become softer and more elastic, losing tensile properties and increasing in ultimate elongation. Also, the coefficient of friction of a PVOH film will increase with increased moisture content.
- the polymer solution can consist of or consist essentially of solvent(s) and base polymer resin(s), with one or more crosslinking agents and optional secondary agents injected into a stream of the polymer solution before application to the surface on which the film is formed.
- the polymer solution can include common processing aids that would find utility in a wide variety of formulations, such as plasticizers, lubricants, release agents, fillers, extenders, antiblocking agents, detackifying agents, antifoams and other functional or decorative ingredients, in amounts suitable for their intended purpose, and one or more crosslinking agents are injected into a polymer solution feed stream and then mixed, before application to the surface on which the film is formed.
- the crosslinking agent may be any chemical agent that can form chemical bonds with the hydroxyl groups of PVOH.
- Such crosslinking agents include, but are not limited to, monoaldehydes (e.g., formaldehydes, hydroxyacetaldehydes, and hydroxyadipaldehydes), dialdehydes (e.g., glyoxal, glutaraldehyde and succinic dialdehyde), aldehyde-containing resins (e.g., trimethylol melamine, melamine formaledehyde), polyfunctional carboxylic acids (e.g., dicarboxylic acids such as maleic, oxalic, malonic and succinic acids), citric acid, glycidyl and other difunctional methacrylates, N-lactam carboxylates, dithiols (e.g., m-benzodithiol), urea-formaldehyde and melamineformaldehyde, dimethyl urea, di-isocyanates, boric acid and borates, salts
- crosslinking agents undergo direct condensation reactions with hydroxyl groups to form covalent bonds (such as esterification and acetalization Atty. Docket No.30658/40658A PATENT APPLICATION
- crosslinking agents can have one or more of the following functionalities: those that form complexes via labile polar covalent interactions, those that crosslink via ionic interactions, those that crosslink via hydrogen bonding interactions, and combinations of such crosslinking agents. All such types of crosslinking agents are contemplated for use in the method described herein.
- An example of a water-soluble polyamide- epichlorohydrin is available under the trade name POLYCUP 172 by Hercules, Inc. of Wilmington, Delaware.
- crosslinking agents are particularly suitable for polyvinyl alcohol and many of the other water-soluble polymers described herein, but other crosslinking agents may be more appropriate or convenient for others of the described water-soluble polymers, and still other crosslinking agents may be more appropriate or convenient for other polymers which can be solution-cast and crosslinked.
- alginates are very conveniently crosslinked by simple calcium salts.
- various crosslinking agents are used with a catalyst, such as an acid catalyst with an aldehyde crosslinker.
- the crosslinking agent preferably is present in an amount up to about 10 % by weight, for example about 1 % to about 10 % by weight, or 5 % to about 10 % by weight, based on the weight of the water-soluble polymer.
- water- soluble polyamide-epichlorohydrin preferably is used in an amount of about 7 - 10 % by weight of a PVOH polymer.
- boric acid is preferably used in an amount of about 5 % by weight of a PVOH polymer.
- Other secondary components can be colorants, such as those soluble in the polymer solution (e.g., an acid dye, direct dye, basic dye, other water-soluble dye, or any combination thereof) and/or those insoluble in the polymer solution.
- colorants such as those soluble in the polymer solution (e.g., an acid dye, direct dye, basic dye, other water-soluble dye, or any combination thereof) and/or those insoluble in the polymer solution.
- the secondary component will be an insoluble particulate.
- a particulate can be used to impart a desired decorative appearance to the resulting film.
- particulates that have one or more properties such as coloration, reflectivity, fluorescence, Atty. Docket No.30658/40658A PATENT APPLICATION
- Insoluble pigments are one type of particulate matter contemplated.
- the particulates can have any morphology, including spherical, crystalline, irregular, and planar.
- the secondary component will be a soluble particulate.
- a shaving or flake of colored water-soluble material e.g., PVOH or gum arabic
- microcapsules can be used as a secondary component.
- a microcapsule with a relatively soft shell e.g., gelatin
- another agent e.g., scent, crosslinking agent
- the degree and timing of shear before casting can be used to control the characteristics of the resulting film.
- a color-containing microcapsule with a relatively rigid shell e.g., gelatin with a degree of crosslinking
- Water-soluble microcapsules or microspheres are preferably slurried in a non- aqueous carrier (e.g., a glycol) prior to injection into an aqueous polymer solution.
- the particulates will have an average particle size of 1 micron to 100 microns. In another embodiment, the particulates will have an average particle size of 4 microns to 25 microns.
- the solids content of the insoluble particulate secondary component in a fluid injected into the polymer solution preferably is in a range of about 3 % by weight, based on the total weight of the polymer solution (wt.%) to about 10 wt.%.
- Other secondary agents can be selected from among plasticizers, lubricants, release agents, fillers, extenders, antiblocking agents, detackifying agents, antifoams and other functional or decorative ingredients, and combinations of any of the foregoing.
- the fluid stream which includes the secondary component can take any desired form, such as, but not limited to, a solution, a suspension, an emulsion, a sol, and a gel.
- a solution such as, but not limited to, a solution, a suspension, an emulsion, a sol, and a gel.
- the secondary component will typically be present in the fluid in a much greater concentration than will be desired in the ultimate film product, resulting in a relatively low flow rate of fluid injection. Accordingly, the fluid including the secondary component will typically be injected into the polymer solution stream in a relatively low ratio of secondary component to polymer solution.
- the ratio can be about 1 : 10 to about 1 : 100 by volume of secondary component to polymer solution, such as with a water-soluble dye.
- the ratio of crosslmking agent to polymer solution can be about 0.3:10 to about 0.3:100, for example.
- the flow rate of fluid containing the secondary component will be on the order of liters or tens of liters per hour whereas the flow rate of polymer solution is on the order of hundreds of liters per hour.
- the flow rate of fluid containing a soluble dye as a secondary component can be in a range of about 0.5 gal./hr (2 1/hr) to about 5 gal./hr (19 1/hr) when the flow rate of polymer solution is about 100 gal/hr (379 1/hr).
- the fluid stream preferably has a sufficient viscosity such that its volumetric flow rate can be accurately measured, hi one embodiment, it is contemplated that the viscosity of the fluid stream containing the secondary component will be at least 30 cps at 185 0 F (85 0 C), for example about 70 cps to about 80 cps at 185 °F (85 0 C). It is contemplated that the fluid can include a glycol, such as propylene glycol, to adjust the viscosity to the desired range, for example when the secondary component is water-soluble, such as a water-soluble dye.
- a glycol such as propylene glycol
- the polymer solution will typically have a relatively high viscosity and solids content.
- the polymer solution can have a solids content of at least about 20 wt.%, or about 25 wt.% to about 40 wt.%.
- the viscosity can be, for example, at least 30,000 cps at 185 0 F (85 0 C), for example about 40,000 cps to about 50,000 cps at 185 °F (85 0 C).
- the pressure of the supplied polymer solution will typically be relatively high, such as at least 100 psi (0.7 MPa), or about 100 psi to about 200 psi (about 0.7 MPa to about 1.4 MPa).
- the fluid containing the secondary component is pressurized to exceed the polymer solution stream pressure at the point of injection, in order to accurately and reliably inject the secondary component into such a pressurized polymer solution stream.
- the degree of overpressure is preferably at least 120% (e.g., 120 psi (0.8 MPa) for a polymer solution pressure of 100 psi (0.7 MPa)).
- a preferred embodiment of a band casting system includes a mixing system, a band casting machine comprising at least first and second rotating drums about which a continuous metal band is tensioned and travels with the rotation of the drums, a polymer applicator such as an adjustable sheeting die or other device used for applying the polymer solution from the tank to the metal band, and a drying chamber enclosing a least a portion of the metal band downline of the sheeting die.
- the overall solvent casting system is generally referenced by the number "10.”
- Other components are similarly and consistently numbered throughout the specification and drawings. While some embodiments disclosed herein are described for use with a particular continuous band casting machine, such as, for example, those designed and manufactured by Berndorf Belt Systems, Inc. of Carpentersville, Illinois, other such band casting machines are be capable of adaptation for implementation of the described method and apparatus.
- a solvent band casting system 10 begins with a mixing system 12 for mixing and storing a polymer solution.
- the mixing system 12 can be a single tank, or in a preferred embodiment may comprise a plurality of tanks and attendant piping, pumps, and valves to control the flow of the polymer solution among the tanks.
- a band casting machine 14 is shown including first and second rotating drums 16 and 18, respectively, about which a continuous loop of metal band 20 is tensioned and travels with the rotation of the drums 16, 18.
- an injection system 82 (shown schematically) coupled to a polymer solution feed line 13 by a conduit junction 84. Downstream of the junction 84 is an in-line mixer 86 (shown schematically in Fig. 1 and in cut-away view as a static mixer in Fig. 4), disposed just prior to the casting die 22.
- the conduit junction 84 can be a manifold, with a plurality of associated injection systems 82 for a plurality of secondary components or component mixtures, each of such components or component mixtures independently added to the polymer solution feed.
- a plurality of secondary components can also be injected at various points along the polymer solution feed system (e.g., as measured by distance from the applicator such as a casting die), due to potential effects on viscosity, component interactions, and targeted characteristics of the product film desired.
- a coating device such as a casting die 22 (e.g. > a sheeting die) is used to apply the polymer solution to the metal band 20 of the casting machine 14.
- a feed line 13 connects the mixing system 12 and injection system 82 to the die 22 and is used to feed the polymer solution from the mixing system 12, through the various optional components and operations, and to the die 22.
- the die 22 (see Fig. 2) comprises an internal chamber (not shown) and a slot-shaped orifice 11 extending across the width of the die 22.
- the gap e.g., determined by an adjustable vertical dimension
- the gap is variable across the width of the die 22 and is used to assist in controlling the thickness of the film produced by the casting system 10. The gap can be monitored and/or adjusted.
- a drying chamber 24 is shown enclosing a portion of the loop of metal band 20 downline of the sheeting die 22.
- the drying chamber 24 of the embodiment shown comprises an upline zone 26 and a downline zone 28.
- Each zone 26, 28 includes a heater (burner) 30 located near an air inlet 32 and an exhaust blower 34 located near an air outlet 38.
- the portion of the metal band 20 within the drying chamber 24 at any given time travels over and is supported by a series of support rollers or idlers 40.
- the embodiment shown in Figure 1 includes a series of idlers 40 representing the combination of idlers and associated sensors for monitoring rotation of the idlers.
- the base polymer solution is first mixed in a batch operation.
- the mixing takes place in the mixing system 12 (see Fig. 1).
- the mixing system 12 includes a bulk handling station 44, a mixer 46 having a mix tank 72, a hold tank 48 and a run tank 50.
- the bulk handling station 44 (shown schematically in Fig. 1) is used for holding at least the polymer raw ingredient for the desired solution, and may include other, secondary components. These ingredients can include various resins, polymers, plasticizers, and other additives.
- the bulk handling station 44 can include a number of vessels or tanks, each corresponding to one or more different ingredients. Each of the tanks or vessels is in flow communication with the mixer 46 for transporting the desired ingredients into the mix tank 72. Additionally, the various ingredients may be manually fed into the mix tank 72.
- the mixer 46 includes a jacketed mix tank 72.
- the mixer 46 also includes a mix motor 78, a mixer shaft 74 and a plurality of mixing blades 76.
- the various mixing blades 76 on the mix shaft 74 provide a combination of high shear mixing and vertical movement of the solution to promote mixing.
- the mix shaft 74 and blades 76 are centrally located within the housing and are operably connected to the mix motor 78.
- the motor 78 is a powerful one of at least about 150 horsepower.
- a suitable motor can be obtained from Morehouse-Cowles of Fullerton, California.
- the means of delivering the ingredients to the mix tank 72 and means of delivery of the solution can include conduits such as piping 80 and 13, respectively, between source and destination in combination with various pumps, as will be apparent to those of ordinary skill in the art.
- the batch mixing process begins by filling or charging the mix tank 72 with water and a variety of components that can include plasticizers, flatting agents, surfactants, and the like. These ingredients may need to be added at different moments of the mixing process due to their potential affect on viscosity, interactions, and targeted characteristic of the product desired.
- the quantity of water can affect both the mixing process as well as the quality of the product produced. Temperature of the solution or suspension is maintained within a controlled range to promote Atty. Docket No.30658/40658A PATENT APPLICATION
- the polymer resin is then added under rapid agitation effected by the mixing blades 76. Varying amounts of water may be added throughout the resin addition to assist in the mixing process.
- the tank temperature set point is adjusted to accelerate dissolution of the resin. As the resin dissolves, viscosity will typically increase, making it necessary to increase the speed of the mix motor 78 to maintain adequate solution movement without causing damage to the solution or mix tank 72.
- the amount of time required to produce a batch of mixed solution depends on the size of the batch and the type of resin.
- the mixed batch of polymer solution is then pumped out of the mix tank 72 to a hold tank 48 or a run tank 50, but typically to a hold tank 48.
- the hold tank 48 is typically used to hold the solution to allow bubbles (e.g., air bubbles) and other imperfections (such as gels or affects due to temperature variation) to rise to the top and be separated from the solution. This preferably occurs while the solution is undergoing mild agitation to maintain the solution. Typically, the hold tank 48 is maintained at a temperature of 185 °F (85 °C) through use of a water or steam jacket to prevent coagulation. Other heating methods are acceptable. An agitator or stirrer (not shown) may also help minimize coagulation of the solution and maintain uniform temperature throughout the tank. Both the temperature and the agitation preferably are monitored and controlled by the controller 36.
- bubbles e.g., air bubbles
- other imperfections such as gels or affects due to temperature variation
- a feed line 13 runs from the hold tank 48 to the run tank 50, from where solution is continuously pumped to the die 22 for casting onto the band 20.
- One or more filters 47 may be placed between the hold tank 48 and the run tank 50, between the run tank 50 and the junction 84, between the junction 84 and the die 22 ,or in a plurality of such locations.
- the secondary component includes an insoluble particulate, then preferably a filter is not disposed between the junction 84 and the die 22.
- FIG. 4 Elevation view
- FIG. 5 plan view
- the injection system includes a reservoir tank 90 for holding a supply of fluid containing secondary Atty. Docket No.30658/40658A PATENT APPLICATION
- the tank can include an associated agitator or mixer (e.g., a stirrer, in-tank eductor, or any other suitable mixer; not illustrated).
- an associated agitator or mixer e.g., a stirrer, in-tank eductor, or any other suitable mixer; not illustrated.
- a positive displacement gear pump 92 and associated AJC motor 94 with a variable frequency drive feed the fluid from the tank 90 via feed line conduit 96.
- a variable frequency drive (not illustrated) feed the fluid from the tank 90 via feed line conduit 96.
- other types of pumps can be used, such as a peristaltic pump.
- a needle valve 98 is disposed in the fluid path between the pump 92 and the junction 84 with the polymer solution feed line conduit 13 to control the fluid pressure.
- the illustrated injection system 82 also includes various optional components. Fluid pressure is monitored with gauge 100.
- the embodiment of the system shown includes a volumetric gear flow meter 102 and a check valve 104 disposed between the needle valve 98 and the junction 84.
- the injection system 82 is shown with a heater 106 disposed between the pressure gauge 100 and the needle valve 98.
- Polymer solution pressure at the point of inj ection is monitored by gauge 110, and downstream pressure after the in-line mixer 86 is monitored by gauge 112.
- the in-line mixer 86 preferably is a static mixer, and can be of any desired length to provide homogeneous mixing of the polymer solution and secondary component.
- the pressure of the fluid supply is adjusted by manually adjusting the needle valve 98 to an amount of approximately 120% of the polymer solution pressure, and then a controller (e.g., a proportional, integral, derivative controller) is used to regulate the fluid flow rate to a desired setpoint.
- a controller e.g., a proportional, integral, derivative controller
- a PID feedback loop can be established by monitoring fluid volumetric flow rate with the gear flow meter 102 and controlling the speed of the pump motor 94 to achieve a desired fluid volumetric flow rate setpoint.
- the volumetric flow rate of the polymer stream can be measured upstream and downstream of the junction 84, and the pump motor 94 speed can be adjusted to achieve the desired difference between the flow rates.
- the band casting machine 14 is further understood with reference to Fig. 3.
- the casting machine 14 is comprised of a first or lead drum 16 and a second or end drum 18. Extending about lead drum 16 and end drum 18 is a continuous loop of metal band 20.
- the drums 16 and 18 travel in the direction indicated by the arrows ⁇ imposing a similar revolution of the band 20.
- the drums are approximately 65 inches wide and 48 inches in diameter, and the band 20 is approximately 61 inches wide with a circumference of approximately 325 feet.
- a suitable band casting machine is available from Berndorf Belt Systems, Inc. of Carpentersville, Illinois.
- the first or lead drum 16 is preferably hollow to allow for pre-heating the band 20 prior to coating with or casting the polymer solution.
- the second or end drum 18 is preferably cooled to assist removal of the final film product.
- the loop of metal band 20 has a production or upper portion 21 and a return or under portion 23.
- the outer surface 25 of the band is used to support the applied polymer solution during drying.
- a plurality of idlers 40 may be spaced along the underside of upper portion of the band 20 to provide support of the band 20.
- the idlers 40 may also be monitored (e.g. , by position sensors for monitoring rotation), to determine movement of the band 20.
- the band 20 can be a very expensive piece of equipment, any complications of production which might tend to damage the band 20, such as an idler that stops rotating (e.g., resulting in the band being dragged across the idler or guiding the band off the edge of the drums 16, 18) can be avoided by monitoring and taking appropriate control action.
- the band 20 will typically travel from a temperature of about 125 °F (52 0 C) at the lead drum 16 to a temperature of about 215 °F (102 °C) at the end drum 18. These temperature changes can affect the tracking of Atty. Docket No.30658/40658A PATENT APPLICATION
- the band 20 on drums 16 and 18.
- the band 20 preferably is made of stainless steel to address the varying thermal gradient of the system existing between the lead drum 16 and the end drum 18.
- Other metals, alloys, plastics, or rubbers, having desired thermal expansion parameters may also be suitable for construction of a casting band 20.
- the process of solvent casting occurs with application of a layer of polymer solution onto the band surface 25.
- polymer solution applicator such as a sheeting die 22 or other coating device.
- a suitable die 22 is commercially available from Extrusion Dies Inc. of Chippewa, Falls, Wisconsin or Cloeren Incorporated of Orange, Texas.
- the sheeting die 22 coats (deposits) a continuous curtain of polymer solution across the width of the band 20.
- the die 22 (see Fig. 2) includes an internal channel (not shown) through which the solution flows. At the end of the channel is a slot-shaped orifice 11 which extends across the width of the die 22.
- An upper surface of the slot is formed by a lip 53 and is deformable with respect to a lower surface 55 of the slot to allow for changes to be made to the dimensions of the slot opening 11.
- a series of threaded bolts 52 across the width of the die are used to vary the dimensions of the slot opening depending upon the direction of rotation of the bolts. Additionally, the bolts 52 may be heated or cooled to control the thickness of the slot 11. The controlled expansion and contraction of the bolts can vary the dimensions of the slot 11.
- compositions are described as including components or materials, it is contemplated that the compositions can also consist essentially of, or consist of, any combination of the recited components or materials, unless described otherwise.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Moulding By Coating Moulds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72813905P | 2005-10-19 | 2005-10-19 | |
PCT/US2006/039470 WO2007047231A1 (en) | 2005-10-19 | 2006-10-11 | Method and apparatus for continuously preparing crosslinked, solution-cast polymer film |
Publications (1)
Publication Number | Publication Date |
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EP1919694A1 true EP1919694A1 (en) | 2008-05-14 |
Family
ID=37845391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP06836237A Withdrawn EP1919694A1 (en) | 2005-10-19 | 2006-10-11 | Method and apparatus for continuously preparing crosslinked, solution-cast polymer film |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1919694A1 (ja) |
JP (1) | JP2009512577A (ja) |
CN (1) | CN101267936A (ja) |
AU (1) | AU2006304040A1 (ja) |
CA (1) | CA2621457A1 (ja) |
WO (1) | WO2007047231A1 (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070085234A1 (en) * | 2005-10-19 | 2007-04-19 | Boyle Timothy J | Method and apparatus for solution casting film with secondary component |
US8282954B2 (en) * | 2008-12-15 | 2012-10-09 | Monosol Rx, Llc | Method for manufacturing edible film |
RU2640589C2 (ru) * | 2012-07-06 | 2018-01-10 | Райн Хеми Райнау ГмбХ | Катализаторы для получения литьевого полиамида, способ их получения и их применение |
CN104738139A (zh) * | 2013-12-30 | 2015-07-01 | 德夫罗有限公司 | 计量泵系统 |
CN106832362B (zh) * | 2016-12-30 | 2023-03-21 | 中国工程物理研究院激光聚变研究中心 | 聚合物薄膜浇铸法制备装置 |
CN108219165B (zh) | 2018-01-15 | 2019-01-25 | 思必康(厦门)新材料有限公司 | 一种聚乙烯醇组合物及制备方法及用途 |
CN109278227B (zh) * | 2018-11-09 | 2024-04-16 | 江苏科润膜材料有限公司 | 增强型全氟离子交换膜的二次流延机构 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4584231A (en) * | 1983-12-02 | 1986-04-22 | Vcf Packaging Films, Inc. | Solvent cast acrylic film |
JPS62214912A (ja) * | 1986-03-14 | 1987-09-21 | Hitachi Chem Co Ltd | ポリイミドフイルムの製造法 |
US5308425A (en) * | 1992-10-22 | 1994-05-03 | Aristech Chemical Corporation | Method of making crosslinked acrylic sheet with enhanced vacuum molding attributes |
PL199269B1 (pl) * | 1999-10-12 | 2008-09-30 | Nippon Catalytic Chem Ind | Sposób wytwarzania porowatego usieciowanego polimeru |
-
2006
- 2006-10-11 WO PCT/US2006/039470 patent/WO2007047231A1/en active Application Filing
- 2006-10-11 CA CA002621457A patent/CA2621457A1/en not_active Abandoned
- 2006-10-11 CN CNA2006800342464A patent/CN101267936A/zh active Pending
- 2006-10-11 AU AU2006304040A patent/AU2006304040A1/en not_active Abandoned
- 2006-10-11 JP JP2008536678A patent/JP2009512577A/ja active Pending
- 2006-10-11 EP EP06836237A patent/EP1919694A1/en not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
See references of WO2007047231A1 * |
Also Published As
Publication number | Publication date |
---|---|
JP2009512577A (ja) | 2009-03-26 |
CN101267936A (zh) | 2008-09-17 |
AU2006304040A1 (en) | 2007-04-26 |
WO2007047231A1 (en) | 2007-04-26 |
CA2621457A1 (en) | 2007-04-26 |
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