Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D1/00—Processes for applying liquids or other fluent materials
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
  • B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
  • B05D3/061—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D2401/00—Form of the coating product, e.g. solution, water dispersion, powders or the like
  • B05D2401/90—Form of the coating product, e.g. solution, water dispersion, powders or the like at least one component of the composition being in supercritical state or close to supercritical state

Definitions

• This invention concerns the use of a process that permits chemical alteration of a fluid during continuous flow of that fluid to a final substrate.
• Multiple types of coating processes provide a means for delivering a fluid, particularly a liquid, from a dispenser to a final substrate. Once the fluid has arrived on the final substrate, the fluid can be altered physically or chemically. Examples of fluid alteration after arrival at the final substrate include continuous polymerization processes, evaporation of solvents, and the like.
• PCT Patent Publication WO 0 031 725 discloses a process for producing an ultra thin solid membrane for gas separation.
• U.S. Pat. No 4,132,824 discloses a method for casting ultra thin methylpentene polymer membranes.
• Japanese Patent Specification JP HEI 2(1990) - 207870 discloses production of an ultra thin film laminate.
• U.S. Pat. No. 5,067,797 discloses a process for casting liquid crystalline polymer solution on a bath.
• Japanese Patent Specification JP 83,035,723 discloses a composite porous and non-porous membrane manufacture by pouring polymer solution onto a water surface, rolling, and winding non-porous membrane obtained onto porous membrane.
• U.S. Pat. No. 5,324,359 discloses a process for depositing droplets and optionally dosing the droplets with radiation as they fall to a substrate.
• World Patent No. 96/23595 discloses a process for coating a two-layer curtain, also known as a carrier fluid process, that uses a carrier layer of fluid (such as water) to transport a functional layer (such as silicone or other polymeric material) to a web.
• a carrier layer of fluid such as water
• a functional layer such as silicone or other polymeric material
• One aspect of the present invention is a method for chemically altering the composition of a first fluid in continuous flow from a dispenser to a final substrate, comprising the steps of dispensing the fluid in a continuous flow from a source location into a second fluid, and imposing at least one condition on the first fluid to alter the chemical composition of the first fluid before that first fluid leaves the second fluid and contacts the final substrate during a coating or extrusion process.
• the first fluid can be a liquid, a gas, a combination of liquid and a gas, a combination of two or more gases, a combination of two or more liquids, a supercritical fluid, a combination of a supercritical fluid and a gas, a combination of a supercritical fluid and a liquid, or a combination of two or more supercritical fluids.
• the second fluid can be a liquid, a gas, a combination of liquid and a gas, a combination of two or more gases, or a combination of two or more liquids as a mixture or as a multilayer, a supercritical fluid, a combination of a supercritical fluid and a gas, a combination of a supercritical fluid and a liquid, or a combination of two or more supercritical fluids.
• the final substrate can be a solid, at least one liquid on a solid, or at least one gas on a liquid.
• the condition can be imposition of a single type of actinic radiation, more than one type of actinic radiation imposed concurrently, or more than one type of actinic radiation imposed sequentially.
• Another condition can be adsorption of a reactive gas into the first fluid.
• Another condition can be transfer of heat to the first fluid by conduction or radiation.
• Another condition can be capture of activating particles or catalysts by the first fluid.
• Another condition can be capture into the first fluid droplets from an activating fog.
• Another condition can be imposition of an electric discharge.
• Another condition can be imposition of an alternating or direct current of electric energy.
• Another condition can be imposition of corona fields.
• Another condition can be imposition of electric fields.
• Another condition can be imposition of magnetic fields.
• Another condition can be imposition of oscillating fields.
• Another condition can be imposition of sound waves.
• Another condition can be imposition of ultrasound.
• Another condition can be imposition of shock waves.
• Another condition can be imposition of pressure waves.
• the dispenser can be an extrusion die, a nozzle, slide die, or other orifice from a source of the first fluid.
• a feature of the present invention is the ability to alter chemical properties of a fluid between the time of its dispensing and the delivery to a final substrate.
• Another feature of the invention is the ability to alter chemical properties in more than one manner from the time of dispensing to delivery.
• An advantage of the present invention is the formation of a different chemical composition of a fluid on a final substrate from the time that the fluid is ejected from its source.
• the second fluid can be inert to, i.e., substantially insoluble in, the first fluid or interactive with the first fluid such that the first fluid is chemically altered during the time of flight through the second fluid and before the first fluid contacts any solid.
• the first fluid can operate within the principles of gravitational flow during imposition of the conditions that changes the chemical composition of that first fluid.
• Any coating and extrusion technique that relies on the transfer of a fluid from a source to a final substrate is suitable for use with the present invention.
• Nonlimiting examples of coating techniques are generally found in the technical literature within treatises such as any of the "Coating Processes” and “Coatings” articles in Kirk-Othmer, Encyclopedia of Chemical Technology, Third and Fourth Editions (Wiley-Interscience, 1979 and 1994, respectively.
• a number of coating techniques are desirable because of their ability to rely on the delivery of a fluid, particular one or more liquids, in precisely measured continuous fluid flows.
• Nonlimiting examples of these coating techniques are curtain coating, slide coating, extrusion die coating, and roll coating which are more completely described in Cohen and Gutoff (Modern Coating and Drying Technology, VCH Publishers, 1992) and in Satas, (Coatings Technology Handbook, Marcel Dekker, Inc. 1991). Additional preferred methods of coating include carrier fluid coating which is more completely described in International PCT Patent Publication No. WO 96/23595 (Melancon et al.). Melancon et al. discloses a process for coating a two-layer curtain, also known as a carrier fluid process, that uses a carrier layer of fluid (such as water) to transport a functional layer (such as silicone or other polymeric material) to a web. The advantage of this process is that it can be used to generate very thin coatings (i.e. less than 1000 A) without solvent dilution.
• carrier fluid process such as water
• a functional layer such as silicone or other polymeric material
• the first fluid can be a liquid, a gas, a combination of liquid and a gas, a combination of two or more gases, or a combination of two or more liquids either mixed or as a multilayer, a molten polymer, molten salts, liquid metals, or supercritical fluids contained in one or more sources and dispensed either concurrently or sequentially in order to undergo a chemical alteration while in continuous flow prior to reaching a final substrate.
• any one or more of the fluids can be destined for the final substrate or can be discarded during the delivery of at least one of the other fluids to the final substrate.
• These discarded fluids are also known as carrier fluids, such as described in Melancon et al. above.
• Nonlimiting examples of first fluids that can be used as carrier fluids include water, hydrophilic liquids, hydrophobic liquids, noble gases, inert gases, and air which are otherwise nonreactive to the condition(s) between dispensing and delivery of the first fluid through the second fluid to the final substrate.
• the composition of the first fluid intended to undergo chemical reaction is otherwise known as the functional fluid.
• functional fluids include monomers, oligomers, pre-polymers, polymers, crosslinking agents, initiators, modifiers, and any other chemical that can exist in fluid form at a single environment of a given temperature, a given pressure, and a given volume and is chemically reactive under any condition imposed during transport of that fluid in continuous flow through a second fluid.
• liquid pre-polymers that are apt to undergo increased polymerization during transport through ambient air with exposure to actinic radiation.
• pre-polymers are silicone pre-polymers either in neat or in solvent, either dispensed alone or with a carrier fluid.
• Functional fluids may be miscible or immiscible with the carrier fluid.
• Preferred functional layer formulations include silicone-urea release formulations (as disclosed in U.S. Pat. No. 5,045,391 (Brandt et al.)); and silicone or fluorosilicone polymers (such as ethylenically unsaturated-, hydroxy-, epoxy- terminated or pendant functional silicone and fluorosilicone pre-polymers); or other release polymers with suitable low surface energy (such as poly(organosiloxanes), fluoropolymers, and the like) as disclosed in PCT publication WO97/12282 as well as polymers useful for adhesives including but not limited to acrylates, silicone ureas, and methacrylates.
• the mole percent of crosslinkable groups is preferably 0 to 20 mole%, more preferably 0 - 15 mole%, and most preferably 0 - 10 mole%.
• both vinyl and alkenyl (number of carbons greater than 2 and less than 10) crosslinking groups may be used.
• the distribution of crosslinks may be unimodal or multimodal, as in the presence of higher molecular weight silicone gums and silicate resins as additives.
• functional layers are selected from the group consisting of prepolymers with terminal and/or pendant crosslinking functionalities including, but not limited to silicone pre-polymers, silicone-urea polymers, acrylate functional polymers, and epoxy functional polymers and fluoropolymers disclosed above.
• the silicone, fluorosilicone and fluoropolymer functional layer pre-polymers have a number average molecular weight ranging from 2,000 - 60,000 Da and 1 - 30,000 mPas, i.e. suitable for solventless coating. Additionally, solvent can be used to dissolve higher molecular weight silicone and fluorosilicone pre-polymers. More preferably, the functional layer pre-polymers have number average molecular weights of 10,000 - 30,000 Da with viscosities of 200 - 20,000 mPas.
• silyl hydride crosslinkers include Dow Corning as homopolymers (Syl-OffTM 7048), copolymers (Syl-Off TM7678) and mixtures (Syl-Off TM7488) used in the amounts corresponding to 1 :1 to 10:1 silyl hydride:vinyl ratio.
• an appropriate amount of an inhibitor can be used to achieve good cure and an adequate pot life.
• a non-limiting example of an inhibitor is a 70:30 ratio of fumarate in benzyl alcohol to achieve good cure and adequate pot life.
• an inhibitor may not be needed for low percent solids dispersions.
• both thermal and ultraviolet (“UV") initiated platinum catalysts can be used in the first fluid.
• platinum thermal catalysts are Dow Corning (Midland, MI) Syl-Off 4000 and Gelest (Tullytown, PA) platinum- divinyltetramethyldisiloxane complex (SIP6830.0 and SIP6831.0).
• a nonlimiting example of a platinum UV catalyst is disclosed in U.S. Pat. No. 4,510,094 (Drahnak). Unlike the thermal catalyst, the UV catalyst does not require an additional inhibitor since the complex is effectively inhibited until exposure to UV.
• Chemical additives or modifiers can be added to the functional layer composition. These chemical additives may include higher molecular weight gums, silicate resins, surface active agents, particulate fillers, etc.
• Nonlimiting examples of silicone gums include vinyl functional gums ranging in number average molecular weights from 60,000 to 800,000 Da available from Gelest (DMS-41, DMS-46, DMS-52) and ethylenically unsaturated organopolysiloxane gums prepared according to U.S. Pat. No. 5,468,815 and 5,520,978 (Boardman) and in European Patent Publication 0 559 575 Al.
• the alkenyl-functional silicones had 2 to 10 carbon atoms with a molecular weight of approximately 440,000 Da.
• silicone gums When silicone gums were used as additives to low viscosity silicone pre-polymers in 100% solids formulations, their molecular weight was preferably less than 800,000 Da, more preferably less than 600,000 Da, and most preferably less than 500,000 Da. Their concentration was preferably less than 20% (w/w) in the silicone pre-polymer, more preferably less than 10% (w/w) and most preferably less than 5% w/w.
• silicate resins include Syl-Off (Dow Corning) 7615, Gelest vinyl Q resin VQM- 135 and VQM- 146 which are provided as dispersions of silicate in silicone.
• the silicate resin is present at 5 to 100% w/w in the silicone pre-polymer, more preferably 0 to 75%, most preferably 0 to 50% (w/w).
• a nonlimiting list of surface active agents include low molecular weight acrylate based surfactants such as Modaflow (Monsanto, St. Louis, MO) and BYK-358 ( BYK-Chemie, Owens Hill, MD), silicone surfactants such as SilwetTM (OSI, Danbury, CT), and fluorochemical surfactants such as Fluorads (3M, St. Paul, MN) and Zonyl (Dupont, Willimington, DE) leveling agents.
• low molecular weight acrylate based surfactants such as Modaflow (Monsanto, St. Louis, MO) and BYK-358 ( BYK-Chemie, Owens Hill, MD)
• silicone surfactants such as SilwetTM (OSI, Danbury, CT)
• fluorochemical surfactants such as Fluorads (3M, St. Paul, MN) and Zonyl (Dupont, Willimington, DE) leveling agents.
• first fluid requires at least one gas or at least one liquid
• particulate solids therein if not disruptive to any of dispensing, transport, or delivery of the first fluid.
• a nonlimiting list of particulate fillers include hydrophobic fumed silica such as CAB-O-SILTM TS-530, TS-5610, and TS-720 (both from Cabot Corp. of Billerica, MA) and AER-O-SILTM R812, R812S, R972, R202 (from Degussa Corp. of Ridgefield Park, NJ).
• the preferred inorganic particles include fumed, precipitated or finely divided silicas.
• a non- limiting list of low surface energy fillers includes hydrophobically treated fumed silica, polymethylmethacrylate beads, polystyrene beads, silicone rubber particles, teflon particles, and acrylic particles.
• Other particulate fillers which can be used but which are of higher surface energy include but are not limited to silica (not hydrophobically modified), titanium dioxide, zinc oxide, iron oxide, alumina, vanadium pentoxide, indium oxide, tin oxide, and antimony doped tin oxide.
• High surface energy particles that have been treated to lower the surface energy are also useful.
• More preferred inorganic particles include colloidal silicas known under the tradenames of CAB-O-SILTM (available from Cabot) and AEROSILTM (available from Degussa).
• CAB-O-SILTM TS-530 is a high purity fumed silica which has been treated with hexame hyldisilazane (HMDZ).
• CAB-O-SILTM TS- 610 is a high purity fumed silica treated with dichlorodimethyl silane. The treatment replaces many of the hydroxyl groups on the fumed silica with trimethylsilyl groups.
• CAB-O-SILTM TS-720 is a high purity fumed silica which has been treated with a dimethyl silicone fluid. As a result the silica is a low surface energy particle.
• the filler is a hydrophobically modified fumed silica treated in situ with HMDZ to chemically bind the silica to the pre-polymer, available from Nusil Corporation (Carpinteria, CA).
• the composition of the hydrophobic filler is preferably 0.1 to 20%, more preferably 0.5 to 10% most preferably 1 to 5% w/w.
• Nonlimiting examples of second fluids include water, hydrophilic liquids, hydrophobic liquids, noble gases, inert gases, and air which are otherwise nonreactive to the condition(s) between dispensing and delivery of the first fluid to the final substrate.
• the second fluid should not interrupt the continuous flow of at least one composition in the first fluid. Desirably, the second fluid does not impede or interrupt the continuous flow of all components of the first fluid until at least one component of the first fluid reaches the final substrate.
• the second fluid is ambient air, nitrogen, or helium if a gas, and water if a liquid.
• Conditions Imposed Conditions imposed that are nonreactive with the second fluid but chemically reactive with the first fluid can be imposition of a single type of actinic radiation, more than one type of actinic radiation imposed concurrently, or more than one type of actinic radiation imposed sequentially.
• the dosage of actinic radiation(s) can vary considerably according to needs of the practitioner of this invention.
• Nonlimiting examples of the types of actinic radiation range across the entire electromagnetic spectrum of wavelengths that deliver energy at different frequencies through the second fluid to the first fluid.
• the actinic radiation can be infra-red, near infra-red, visible, or ultraviolet light, heat waves, electron-beam radiation, microwave radiation, excimer laser, excimer lamps, corona-treatment, x-rays, or gamma radiation conventionally used in polymerization processes.
• the dosage of actinic radiation imposed on the first fluid can range from energy fluxes, expressed in energy per unit exposed area, ranging from about 1 mJ/cm 2 to about 100 mJ/cm 2 in the case of light, to energy fluxes, expressed in mRads per unit exposed area, ranging from about 1 mRad/cm 2 to about 000 mRad/cm 2 in the case of other types of radiation.
• the source of actinic radiation can be any locus or combination of loci that generates radiation of the particular wavelength(s) desired, ranging from the sun to "black lights” to medium pressure mercury lamps to cobalt radiation sources, all known to those skilled in the art for providing energy for chemical reaction of a fluid on a solid or in another liquid.
• the amount of radiation dosage depends on the amount of chemical reaction desired for the first fluid while in transport from the dispenser through the second fluid to the final substrate.
• amounts of chemical reaction include full polymerization of the pre-polymer before it reaches the final substrate; partial polymerization of the pre-polymer that provides "green strength," useful rheological properties, or other temporary handling advantages between dispensing of the first fluid as a liquid and delivery of the pre-polymer to the final substrate for further processing; or some combination of types of chemical reaction either operating concurrently or sequentially before the first fluid reaches the final substrate.
• a staged chemical reaction of two liquid monomers emerging from a dispenser can form a pre-polymer followed by merging of that first fluid with a flow of crosslinking agent that then completes the polymerization before the first fluid reaches the final substrate.
• a flow of crosslinking agent that then completes the polymerization before the first fluid reaches the final substrate.
• the condition(s) imposed on that fluid have chemically transformed that object into a solid for landing on the final substrate.
• the final substrate can be merely a landing spot for the chemically altered first fluid or can be a major surface of a final product that is improved by the coating of the chemically altered first fluid on that major surface.
• Nonlimiting examples of final substrates can be continuous belts, discrete sheets or parts, cylindrical rolls, spheres, particles, frames, and the like.
• the surfaces which the chemically altered first fluid contact can have a variety of surface properties that can alter the physical appearance of the chemically altered first fluid upon contact with the substrate.
• Nonlimiting examples of the surface properties include porous, microporous, and nonporous surfaces; textured, microreplicated, embossed, or other patterned surfaces; particulate loaded or smooth surfaces; high surface energy or low surface energy surfaces; opaque, clear, translucent, or optically colored surfaces; and radiation sensitive or radiation tolerant surfaces.
• the final substrate In the event that it is preferred that the final substrate not be exposed to the actinic radiation that imposes the conditions that chemically alter the first fluid while in the second fluid, then optionally but preferably, the final substrate can be shielded from the source of actinic radiation without otherwise shielding the first fluid while moving through the second fluid.
• the final substrates that are intended for temporary landing spots for the chemically altered first fluid can have any of the above surface properties but preferably have major surfaces with suitable surface energy for providing desired wetting properties of the altered first fluid or facilitated subsequent release.
• Nonlimiting examples of temporary landing spots include webs that have silicone- containing release surfaces for removal of a liquid that has been polymerized during transport through air, such as the polymerization of liquid monomers to form an adhesive sheet before such sheet contacts a release liner, and a polymeric web with or without a primer to promote wetting and adhesion by a silicone release on a liner.
• the final substrates that are intended for permanent sites for the chemically altered first fluid can be any of the final substrates intended for temporary landing spots or can be any other substrate that has any of the above surface properties.
• the composition of the final substrate can be metallic, ceramic, or polymeric; naturally occurring or synthetically derived; and crystalline or non- crystalline.
• nonlimiting examples of the products that can employ the process of the present invention include electrographic imaging equipment (such as electrophotographic webs or electrostatic transfer agents); bandages, abrasives, adhesives on release liners, optical and reflective laminates, fabrics, membranes, films, and the like.
• a particularly suitable use of the present invention is the delivery of a functional fluid to a low energy surface substrate where an increase in viscosity of the fluid is needed between the time of dispensing and the time of delivery to the substrate. This use minimizes the need for use of primers on the low energy substrate in order to accept coating of the first fluid in a chemically unaltered state.
• Another particularly suitable use of the present invention is the delivery of a functional fluid that generates a considerable exotherm during chemical alteration that would otherwise damage the final substrate.
• Use of the second fluid as a heat sink can minimize thermal damage to the final substate while providing a coating process and combination of functional layer and substrate previously unavailable.
• Another particularly suitable use of the present invention is the delivery of a functional fluid to a radiation sensitive substrate, such that irradiation of the first fluid prior to contact with a shielded substrate prevents damage to the substrate.
• the substrate may include polyester terephthalate, polycarbonate, polystyrene, and inverted dual layer photoreceptor as described in Example 6 of PCT Patent Publication WO 96/34318. Most preferably, the substrate is clear polyester.
• Shield A shield may optionally be used to protect the final substrate from actinic radiation or results of the chemical alteration process (e.g., an exotherm) while not adversely affecting the flow of the first fluid through the second fluid.
• shields include metal plates, ceramics plates, foam boards, and the like.
• the delivery of the first fluid in a chemically altered state to the final substrate does not end the possibilities of usefulness of the present invention. Any conventional coating or processing technique of a fluid on a substrate can then be employed to further alter either the physical or chemical properties or both of the first fluid, the substrate, or both.
• Nonlimiting examples of post-delivery treatment include embossing, patterning, smoothing, stirring, polymerization, heating, solvent evaporation, calendaring, and the like.
• a particular utility of the present invention is the partially or fully curing of a polymeric material in combination with a carrier fluid coating (as described in Melancon et al. WO 96/23595) or curtain coating which has the advantage of changing the material properties of the formulation in-situ for the purpose of controlling the coating properties.
• a low viscosity, curable formulation can flow freely out of a coating die and then be partially (or fully) cured on a fluid curtain, thereby increasing the viscosity of the formulation that is to be deposited on the substrate.
• Another utility of the present invention is the use of this curing method for in-process polymerization of pre-polymers before they contact a heat or light sensitive substrate or multilayer coating, since the substrate itself would receive minimal exposure. Both thermal and radiation cure processes are envisioned in this invention.

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• Physics & Mathematics (AREA)
• Engineering & Computer Science (AREA)
• Plasma & Fusion (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Chemically Coating (AREA)

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• 1997
  • 1997-12-23 CN CN97182093A patent/CN1095700C/zh not_active Expired - Fee Related
  • 1997-12-23 AU AU57100/98A patent/AU5710098A/en not_active Abandoned
  • 1997-12-23 BR BR9714656-0A patent/BR9714656A/pt not_active Application Discontinuation
  • 1997-12-23 EP EP97953329A patent/EP0971798A1/en not_active Withdrawn
  • 1997-12-23 WO PCT/US1997/023509 patent/WO1998045054A1/en not_active Application Discontinuation
  • 1997-12-23 JP JP54274498A patent/JP2001524869A/ja active Pending
  • 1997-12-23 KR KR1019997009073A patent/KR20010005995A/ko not_active Application Discontinuation
• 1998
  • 1998-03-10 TW TW087103505A patent/TW464666B/zh not_active IP Right Cessation
  • 1998-04-02 ZA ZA9802820A patent/ZA982820B/xx unknown

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