Patent Application
20180250707
A multilayer article comprising a fluoropolymer release coating, which minimizes sticking, is described along with methods of making such an article.
Fluorinated polymers such as polymers of tetrafluoroethylene (TFE) are well known for their superior heat resistance, chemical resistance, corrosion resistance, and anti-stick properties. Because of these properties, polymers of TFE have found a wide range of applications including use as release (also called non-stick) coatings on metal substrates such as cookware including cook, bake, and frying articles.
It is known that the adhesion of fluoropolymers to metal is rather low, so in the fabrication of such cookware it is customary to apply a primer composition to the metal before applying the fluoropolymer topcoat to improve adhesion of the topcoat fluorinated polymer layer to the metal substrate.
Often times the primer composition includes a fluorinated polymer to aid in the adhesion of the fluoropolymer topcoat to the underlying primer layer. Because fluorinated polymers are typically more expensive than their hydrogenated counterparts, it is desirable to use a thin layer of the primer composition (i.e., use less fluorinated polymer). Thin coating layers (e.g., less than 10 micrometers) can be achieved with dispersion coatings, however these dispersions comprise a solvent (such as water and/or organic compounds), which is removed to form the resulting coated layer.
There is a desire for an alternative method of making a primer layer for multilayer articles having a release surface, wherein the primer layer is a thin layer, formed without the use of solvents.
In one aspect, a release surface coated substrate is described made by a process comprising:
delivering particles from at least one fluid jet to a metal surface to impregnate the metal surface with the fluoropolymer to form a first fluoropolymer layer, wherein the particles comprise an abrasive particle, a binder, and a first fluoropolymer;
coating the first fluoropolymer layer with a second fluoropolymer to form a second fluoropolymer layer and thereby forming a multilayered article; and
sintering the multilayered article to form the release surface coated substrate.
In another aspect, a process for forming a release surface on a substrate is described the process comprising:
delivering particles from at least one fluid jet to a metal surface to impregnate the metal surface with a fluoropolymer to form a first fluoropolymer layer, wherein the particles comprise an abrasive particle, the fluoropolymer, and a binder;
coating the first fluoropolymer layer with a second fluoropolymer to form a second fluoropolymer layer and thereby forming a multilayered article; and
sintering the multilayered article to from the release surface coated substrate.
The above summary is not intended to describe each embodiment. The details of one or more embodiments of the invention are also set forth in the description below. Other features, objects, and advantages will be apparent from the description and from the claims.
As used herein, the term
“a”, “an”, and “the” are used interchangeably and mean one or more; and
“and/or” is used to indicate one or both stated cases may occur, for example A and/or B includes, (A and B) and (A or B).
Also herein, recitation of ranges by endpoints includes all numbers subsumed within that range (e.g., 1 to 10 includes 1.4, 1.9, 2.33, 5.75, 9.98, etc.).
Also herein, recitation of “at least one” includes all numbers of one and greater (e.g., at least 2, at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.).
Shown in
The metal substrates of the present disclosure include those substrates typically found useful in cookware articles such as metals selected from carbon steel (e.g., high-carbon steel, stainless steel, aluminized steel), stainless steel, aluminum, aluminum alloys, and combinations thereof.
First fluoropolymer layer 14 is positioned between the metal substrate and the second fluoropolymer layer and is used to attach the second fluoropolymer layer 16 to the metal substrate 12. To form strong adhesion between the metal substrate and the second fluoropolymer layer, it is advantageous for the first fluoropolymer layer to continuously contact both the metal substrate and the second fluoropolymer layer.
The first fluoropolymer layer comprises a first fluoropolymer and a binder. The first fluoropolymer is perfluorinated (i.e., contains fluorine-carbon bonds and no hydrogen-carbon bonds along the polymer backbone) or partially fluorinated (i.e., contains both fluorine-carbon bonds and hydrogen-carbon bonds along the polymer backbone). In one embodiment, the first fluoropolymer layer comprises a melt-flowable fluoropolymer, wherein the fluoropolymer is a copolymer. In one embodiment, the first fluoropolymer is derived from copolymers of tetrafluoroethylene (TFE) and perfluoroolefins having 3 to 8 carbon atoms such as HFP (hexafluoropropylene); copolymers of TFE and PAVE (perfluoro(alkyl vinyl ethers)), wherein the PAVE are linear or branched having 1 to 5 carbon atoms (for example PMVE (perfluoro(methyl vinyl ether)), PEVE (perfluoro(ethylvinyl ether)), PPVE (perfluoro(propylvinyl ether))); and combinations thereof. In one embodiment the first fluoropolymer is derived from copolymers of TFE and CTFE (chlorotrifluoroethylene). In one embodiment, TFE copolymers include ETFE (ethylene-tetrafluoroethylene), PFA (TFE/PAVE copolymer), TFE/HFP/PAVE wherein PAVE is PEVE and/or PPVE, and MFA (TFE/PMVE/PAVE wherein the alkyl group of PAVE has at least 2 carbon atoms). In one embodiment, the first fluoropolymer is derived from monomers selected from vinylidene fluoride (VDF) such as polyvinylidene fluoride (PVDF), and THV (tetrafluoroethylene-hexafluoropropylene-vinylidene fluoride copolymer).
In one embodiment, the fluoropolymer of the first fluoropolymer layer of the present disclosure also comprises reactive groups. Such reactive groups include:
(A) —COX groups wherein X is OH, ONa, OK, NH2, F, or Cl;
(B) —S(═O)2X groups wherein X is OH, ONa, OK, NH2, F, or Cl;
(C) —CH2OSO2Y (sulfate) groups wherein Y═OH, ONa, or OK;
(D) —CH2OH groups; and
(E) phosphate groups such as —PO3− and —OPO3−.
The reactive groups (A)-(E) are terminal groups located at the ends of the fluoropolymer chains or on a side chain along the main carbon backbone of the first fluoropolymer. In one embodiment, the first fluoropolymer comprises at least 2, 3, 5, 10, 50, 100, 500, or even 1000; and at most 5000, 7000, or even 10000 of these groups per 1 million carbon atoms.
These reactive groups can be introduced into the fluoropolymer during its polymerization (e.g., aqueous emulsion polymerization) and/or through the use of particular monomers, initiators, chain transfer agents, etc. Exemplary introduction of these reactive groups is disclosed further below.
The terminal (A) groups can be formed through the use of a radical forming initiator such as persulfate, such as ammonium or potassium persulfate, or a permanganate such as potassium permanganate. Alternatively or additionally, the fluoropolymer may comprise the terminal (A) groups because it is polymerized with monomers comprising the —COX groups or groups that can be converted into the —COX groups (e.g., nitrile groups). Exemplary comonomers include functionalized vinyl ethers or maleic anhydride. Alternatively or additionally, the terminal (A) groups may be formed when a chain transfer agent comprising a —COX group is used during the polymerization. The fluoropolymers comprising the terminal (A) groups can be determined by FT-IR using the method as described in columns 4 and 5 of U.S. Pat. No. 4,743,658 (Imbalzano et al.).
The terminal (B) groups can be formed through the use of persulfate/sulfite initiator systems. For example —SO3− groups can be favored based on the ratio of persulfate/sulfite used. In one embodiment, —SO3− groups are present along with —COX groups. Alternatively or additionally, the fluoropolymer may comprise the terminal (B) groups because it is polymerized with monomers comprising —S(═O)2X groups. Alternatively or additionally, the terminal (B) groups may be formed when a chain transfer agent comprising a —S(═O)2X group is used during the polymerization.
The terminal (C) groups can be formed through the use of a persulfate initiator, such as ammonium or potassium persulfate.
The fluoropolymer may comprise the terminal (D) groups, when the fluoropolymer is polymerized with monomers containing these phosphate groups. The monomers may be non-fluorinated or fluorinated.
In one embodiment, the first fluoropolymer is a particle comprising a core-shell structure with respect to the reactive groups, wherein the particle comprises more reactive groups at the surface of the particle as compared to the center of the particle. Such constructions can occur in thermoplast materials and PTFE-type materials.
Exemplary types of fluoropolymers for use in the first fluoropolymer layer include:
(I) Non-melt processable, fluoropolymer material such as non-melt processable PTFE. Non-melt processable PTFE materials having a standard specific gravity (SSG) of around 2.20 to 2.14 g/cm3 as measured according to ASTM 4895-10. In one embodiment, these non-melt processable fluoropolymer comprise more than 5, 10, 20, 30, 50, or even 100 reactive groups per 1,000,000 carbon atoms. In one embodiment, the non-melt processable PTFE materials is part of a core-shell particle, wherein the outer shell is a non-melt processable PTFE having groups (A) or (B) present in their outer shell, wherein the shell comprises no more than about 10% or even 1% by weight of the particle.
(II) Melt processable fluoropolymers as further described below. In one embodiment, these melt processable fluoropolymer materials comprise at least 10, 30, 50, 100, 150, 200, or even 250 reactive groups per 1,000,000 carbon atoms.
(IIA) Melt processable PTFE materials. Such melt processable PTFE materials include, for example, a micropowder having a melt flow index (MFI) at 372° C./5 kg of 0.001 to 1000 g/10 min and having more than 10, 50, preferably more than 200 of at least one of groups (A)-(D) per million carbon atoms.
(IIB) Perfluorinated thermoplasts such as PFA or FEP copolymers. PFA is a melt processable polymer comprising TFE and a perfluoroalkyl vinyl ether, which can be modified with HFP and/or perfluorinated vinyl ethers. These PFA polymers have a melting point from 270 to 315° C. and a MFI at 372° C./5 kg of 0.1 to 1000 g/10 min. FEP is a melt processable polymer comprising TFE and HFP. In some embodiments, the FEP polymer may be modified with up to 3 wt % of a vinyl ether. These FEP polymers have a melting point from 200 to 280° C. and a MFI at 372° C./5 kg of 0.1 to 100 g/10 min. In one embodiment, the perfluorinated thermoplasts is a PFA or FEP having more than 10, preferably more than 100 of at least one of groups (A)-(D) per million carbon atoms
(IIC) Partially fluorinated thermoplasts such as THV; ETFE; and ETFE polymers further modified with HFP, vinyl ethers and/or partially fluorinated olefins of the structure CH2═CH—Rf, wherein Rf is a partially or fully fluorinated alkyl group. Depending on the initiator system used for polymerization, these polymers may comprise —COX groups, —CH2OH, and/or CH2—O—SO2Y terminal groups. These ETFE and modified ETFE polymers have a melting point from 180 to 280° C. and a MFI at 297° C./5 kg of 0.01 to 1000 g/10 min. The THV polymers have a melting point of 100-250° C. and a MFI at 265° C./5 kg of 0.01-1000 g/10 min. Other partially fluorinated thermoplast materials include polychlorotrifluoroethylene, ethylyene-chlorotrifluoroethylene copolymer, and PVDF.
In addition to the first fluoropolymer described above, the first fluoropolymer layer further comprises a binder. The binder is a non-fluorinated polymer (i.e., a macromolecule derived from repeating monomeric units having a molecular weight greater than 1000 g/mol), which aids in the bonding of the first fluoropolymer layer to the metal substrate.
In one embodiment, the binder is selected from at least one of polyimides, polyamides, polybenzimidazoles, polyamide-imides, polysulfones, polybismaleimides, liquid crystal polymers, polyethersulfone, polyphenylene sulfide, polybenzoxazine, epoxy resin, polyarylene etherketone, and mixture thereof.
Typically the amount of binder to the first fluoropolymer is from 5:95 to 95:5.
In addition to the fluoropolymer and binder described above, the first fluoropolymer layer may further comprise inorganic materials such as carbon black; oxides such as titanium dioxide, silicon dioxide, and magnesium oxide; nitrides such as boron nitride, and silicon nitride; carbides such as silicium carbide; phosphate salts such as sodium, calcium, potassium, and magnesium salts; fluorides such as fluorspar and kryolith; tetralkyl ammonium salts; hydroxyl apatite; and combinations thereof.
As will be described below, a solventless process is used to make thin layers of the first fluoropolymer layer. In the present disclosure, the first fluoropolymer layer has a thickness of at least 0.5 micrometers and no more than 5, 6, 8, 9, or even 10 micrometers.
The second fluoropolymer layer 16 is a durable fluoropolymer layer used to provide an easy release coating to the underlying metal substrate. Such durable fluoropolymer layers comprise a second fluoropolymer such as: polytetrafluoroethylene, or copolymers of tetrafluoroethylene with a perfluorinated monomer. Exemplary perfluorinated monomers include: perfluorinated vinyl ether such PMVE, PEVE, and perfluoro n-propyl vinyl ether (PPVE-1), perfluoro-2-propoxypropylvinyl ether (PPVE-2), perfluoro-3-methoxy-n-propylvinyl ether and perfluoro-2-methoxy-ethylvinyl ether; or a perfluorinated C3 to C8 olefin, such as, for example, HFP. The term ‘perfluorinated monomer’ as used in connection with the present disclosure not only includes monomers consisting of carbon and fluorine atoms, but also includes monomers in which some of the fluorine atoms are replaced by chlorine or bromine such as for example in chlorotrifluoroethylene. Nevertheless, a perfluorinated monomer as used herein does not have carbon-hydrogen bonds in the molecule.
In one embodiment, the second fluoropolymer layer comprises a non-melt processable fluoropolymers. By the term ‘non-melt processable’ is meant that the melt viscosity of the homo- or copolymer of TFE is so high that conventional melt processing equipment cannot be used to process the polymer. This means in general that the melt viscosity is at least 1010 Pascal·seconds. In one embodiment, the second fluoropolymer layer comprises at least 1, 2, 4, 5, or even 10%; and at most 75, 80, 90, 95, 99, or even 100% by weight of a non melt-processable polymer based on the total weight of the polymer.
In one embodiment, the second fluoropolymer layer may comprise a perfluorinated melt-processable fluoropolymer such as e.g., a copolymer of TFE that is melt-processable. Examples of such copolymers include FEP or PFA polymers. In one embodiment, the second fluoropolymer layer comprises at least 1, 2, 4, 5, or even 10%; and at most 75, 80, 90, 95, 99, or even 100% by weight of a melt-processable polymer based on the total weight of the polymer.
Typically, the second fluoropolymer layer comprises additives to improve, for example, the durability, scratch resistance, and/or aesthetics of the layer. Exemplary additives include, colloidal silica, mica, fillers (such as carbon black, silicium nitride, boronitride, titanium carbonitride, etc.), coloring agents, levelling agents, adhesion promoters and tackifiers. The composition may further include in particular film hardeners as disclosed in WO 96/13556 (Tannenbaum). Examples of film hardeners include silicate compounds, such as metal silicates e.g. aluminium silicate, and metal oxides such as titanium dioxide, and aluminium oxide, and carbides e.g. silicium carbide. Typically, these additives are added in the second fluoropolymer layer in a weight % of no more than 1, 2, 5, 8 or even 10%.
Typically the second fluoropolymer layer has a thickness of at least 10, 20, 25, 50, 75, or even 100 micrometer; and at most 500, 600, 800, or even 1000 micrometers.
In one embodiment, second fluoropolymer layer is the topcoat layer. In another embodiment, second fluoropolymer layer 16 is an intermediate layer and thus, the multilayer article comprise additional layer 18. Additional layer 18 may include those layers known in the art, to enhance the properties and/or performance of the multilayer article, such as chemical resistance, smoothness, or gloss. For example, additional layer 18 may be a topcoat layer substantially comprising PTFE, in other words comprising no more than 5%, or even 1% by weight of a non-PTFE polymer. In another embodiment, additional layer 18 is a fluorothermoplast polymer layer substantially comprising PFA or FEP in other words comprising no more than 5%, or even 1% by weight of a non-PFA or non-FEP polymer.
Although
The present disclosure provides a method for making multilayered articles, wherein the primer layer is formed by bombarding a metal substrate with abrasive particles, a first fluoropolymer, and a binder so as to impregnate the metal surface with the fluoropolymer and binder to form the first fluoropolymer layer. This process can generate thin layers of the first fluoropolymer layer onto a metal substrate in the absence of solvents.
In the present disclosure, the metal substrate may be smooth or roughened. In one embodiment, the metal substrate is treated before use. The metal substrate may be chemically treated (e.g., chemical cleaning, etching, etc.) or abrasively treated (e.g., grit blasting, microblasting, water jet blasting, shot peening, ablation, or milling) to clean or roughen the surface prior to use. Because the presently disclosed method comprises abrasively treating the metal surface during the application of the fluoropolymer and binder, advantageously, in one embodiment, the metal substrate is not treated prior to use.
In one embodiment, the metal substrate's surface is treated with abrasive particles such that the substrate's surface becomes partially coated (for example less than 90, 80, 75, 50, or even 25%) with silicon dioxide. The silicon dioxide containing surface can be further modified, for example with silanes prior to the coating of the first fluoropolymer layer. Such treatment is described in U.S. Pat. No. 5,024,711 (Gasser et al.) and U.S. Pat. No. 5,185,184 (Koran et al.)). This pre-treatment method can provide a durable layer with strong adhesive strength.
The first fluoropolymer layer of the present disclosure is provided through treating the metal substrate by impacting the surface of the metal substrate simultaneously with abrasive particles, a binder, and a first fluoropolymer, and optionally in the presence of additives such as inorganic salts. Conventional surface bombardment techniques such as grit blasting, sand blasting, or shot peening can be used.
The abrasive impact should be conducted with sufficient energy (abrasive particle having sufficient size, and hardness) to either roughen the metal surface and/or breech the oxide layer, allowing a window of opportunity for the first fluoropolymer and/or binder to be taken up by or incorporated into the metal substrate before the oxide layer reforms around it.
In one embodiment, the abrasive particle has a particle size ranging from 0.1 μm to 10000 μm, such as a particle size ranging from 1 μm to 5000 μm, or a particle size ranging from 10 μm to 1000 μm.
In one embodiment, the abrasive particle has a Mohs hardness ranging from 3 to 10, such as a Mohs hardness ranging from 4 to 10, or a Mohs hardness ranging from 5 to 10.
Exemplary abrasive particles include, but are not limited to, shot or grit made from silica, alumina, zirconia, barium titanate, calcium titanate, sodium titanate, titanium oxide, glass, biocompatible glass, diamond, silicon carbide, calcium phosphate, calcium carbonate, metallic powders, titanium, stainless steel, hardened steel, carbon steel chromium alloys or any combination thereof.
The first fluoropolymer and binder are delivered simultaneously with the abrasive particles.
In one embodiment, the surface of the metal substrate is bombarded with abrasive particles, binder particles, and first fluoropolymer particles. Typically, the weight ratio of abrasive particles to fluoropolymer particles is from 1:1 to 100000:1.
In another embodiment, the surface of the metal substrate is bombarded with abrasive particles comprising a superficial layer of the first fluoropolymer and the binder. In this embodiment, an abrasive particle core comprises an outer layer that comprises both the first fluoropolymer and the binder. In one embodiment the outer surface of the abrasive particle is substantially covered with fluoropolymer and the binder, for example, at least 75, 80, 90, 95 or even 100% of the abrasive particles surface is covered with a fluoropolymer and binder. In another embodiment the outer surface of the abrasive particle is partially covered with the fluoropolymer and binder, e.g., less than 90, 80, 70 or even less than 30% covered.
In another embodiment, the surface of the metal substrate is bombarded with abrasive particles comprising a superficial layer of the first fluoropolymer and binder particles. In this embodiment, an abrasive particle core comprises an outer layer that comprises the first fluoropolymer. In one embodiment the outer surface of the abrasive particle is substantially covered with fluoropolymer, for example, at least 75, 80, 90, 95 or even 100% of the abrasive particles surface is covered with a fluoropolymer. In another embodiment the outer surface of the abrasive particle is partially covered with the fluoropolymer, e.g., less than 90, 80, 70 or even less than 30% covered.
In another embodiment, the surface of the metal substrate is bombarded with abrasive particles comprising a superficial layer of the binder and particles of the first fluoropolymer. In this embodiment, an abrasive particle core comprises an outer layer that comprises the binder. In one embodiment the outer surface of the abrasive particle is substantially covered with the binder, for example, at least 75, 80, 90, 95 or even 100% of the abrasive particles surface is covered with a binder. In another embodiment the outer surface of the abrasive particle is partially covered with the binder, e.g., less than 90, 80, 70 or even less than 30% covered.
The abrasive particles, binder, and first fluoropolymer are impacted onto the surface of the metal substrate using pressure from a fluid jet. Gaseous carrier fluids such as nitrogen, argon, carbon dioxide, helium, air, and combinations thereof, can be used to deliver the abrasive particles and the fluoropolymer. In the present disclosure, the process is conducted in the absence of liquids, which can be advantageous from a cost perspective. For example, there is no need for drying and venting steps required with liquid coatings and no volatile organic solvents are used.
The pressure of the fluid jet will also be a factor in determining the impact energy of the abrasive particles. If using abrasive particles, binder particles, and fluoropolymer particles comprising the first fluoropolymer, the particles do not have to be delivered to the surface of the metal substrate through the same jet. More than one fluid jet could be used as long as the abrasive particles, binder particles, and the fluoropolymer particles are delivered to the surface at the substantially the same time. In one embodiment, the fluoropolymer particles, binder particles, and abrasive particles are contained in the same reservoir and are delivered to the metal surface from the same jet (nozzle). In another embodiment, the fluoropolymer particles, binder particles, and abrasive particles are contained in separate reservoirs, and multiple nozzles deliver the fluoropolymer, binder, and abrasive particles. The multiple nozzles can take the form of a jet within a jet, i.e., the particles from each jet bombard the surface at the same incident angle. In another embodiment, the multiple nozzles are spatially separated so as to bombard the surface at different incident angles yet hit the same spot on the surface simultaneously.
In one embodiment, the at least one fluid jet is selected from dry shot peening machines, dry blasters, wheel abraders, grit blaster(s), sand blasters(s), and micro-blasters. In one embodiment, the at least one fluid jet operates at a pressure ranging from 0.5 to 100 bar, such as a pressure ranging from 1 to 30 bar, or a pressure ranging from 3 to 10 bar.
In other embodiments, blasting equipment can be used in conjunction with controlled motion such as CNC or robotic control.
One of ordinary skill in the art can appreciate the effect of the size, shape, and hardness of the abrasive material used on the extent of impregnation of the fluoropolymer in the surface using these mixed media.
One of ordinary skill in the art can appreciate the effect of the fluid stream itself, the blasting equipment using a gas medium (typically air) and the effects of using inert gases as a carrier fluid e.g. N2 or noble gases such as Ar and He on the extent of impregnation of the fluoropolymer in the surface.
After bombarding the surface with the abrasive particles, binder, and fluoropolymer to form the first fluoropolymer layer, the first fluoropolymer layer optionally can be sintered and/or baked prior to the application of the second fluoropolymer layer. In one embodiment, it is believed that the blasting of the metal surface with the abrasive particles may cause sufficient localized heating to melt a melt-processable fluoropolymer and/or the binder.
In the present disclosure, the first fluoropolymer layer is in direct contact with the metal substrate, meaning that the first fluoropolymer layer contacts at least 10, 20, 50, 75, 80, 90, 95, or even 100% of the surface of the metal substrate.
In one embodiment, the surface of the metal substrate is treated for a sufficient time to produce a continuous first fluoropolymer layer over the metal substrate surface having a thickness of at least 0.5 micrometers and no more than 5, 6, 8, 9, or even 10 micrometers.
Although not wanting to be bound by theory, it is believed that the abrasion of the particles on the metal substrate provides some roughening of the substrate surface, which may result in the fluoropolymer coating being bound mechanically to the substrate. Alternatively or additionally, is also believed that the reactive or polar groups of the fluoropolymer in the first fluoropolymer layer interact with the metal substrate, forming a chemical bonding to the substrate. However, as the binder is used to assist in the adhesion of the first fluoropolymer layer to the metal, in one embodiment, there is no need for the first fluoropolymer to comprise reactive groups, which may be of particular value when the first fluoropolymer is a non-melt processable PTFE.
After forming the first fluoropolymer layer, the second fluoropolymer layer can be applied directly onto the first fluoropolymer layer using techniques known in the art, for example, using a powder coating or as an dispersion. For example, the second fluoropolymer layer can be applied in the form of an aqueous dispersion, wherein the fluoropolymer latex and optional additives are blended together and then coated onto the first fluoropolymer layer. Alternatively, the fluoropolymer particles and optional additive are dry blended together and coated onto the first fluoropolymer layer.
The second fluoropolymer layer composition may be applied by any of the known techniques to apply coatings to substrates including for example spray coating, roller coating, curtain coating or coil coating the composition.
Following application of the second fluoropolymer layer composition, the multilayer article is generally dried by subjecting the article to elevated temperature of 100 to 300° C. One or more additional layers of non-melt processable PTFE may be then be provided in a similar way. Such one or more layers of PTFE may or may not comprise melt-processable fluoropolymers such as melt-processable copolymers of TFE. When such melt-processable TFE copolymers are used, the ratio thereof may be varied in a multilayer coating so as to create a gradient of increasing amount of PTFE towards the top coating. Like-wise, the ratio of the non-fluorinated polymer to the PTFE particles may be varied to create a gradient of decreasing amount of non-fluorinated polymer towards the top coating.
Following application of the one or more coatings, the obtained multi-layered article (comprising the first fluoropolymer layer and the second fluoropolymer layer) is sintered (i.e., processed above the melting temperature of the highest melting component, such as the binder, first fluoropolymer, or second fluoropolymer). Generally, sintering is carried out in an oven at a temperature of 350° C. to 450° C., typically from 370° C. to 420° C. The sintering time may vary from 1 to 10 min. and the oven may have a constant temperature or an increasing temperature profile may be used, i.e. the temperature may be increased from an initial lower temperature to a higher temperature later in the baking cycle. Generally, processing of the multilayered article is carried out by conveying the coated article through an oven with an increasing temperature profile from entrance to exit.
Exemplary embodiments which are useful for understanding the present disclosure include:
A release surface coated substrate made by a process comprising:
delivering particles from at least one fluid jet to a metal surface to impregnate the metal surface with the fluoropolymer to form a first fluoropolymer layer, wherein the particles comprise an abrasive particle, a binder, and a first fluoropolymer; coating the first fluoropolymer layer with a second fluoropolymer to form a second fluoropolymer layer and thereby forming a multilayered article; and
sintering the multilayered article to form the release surface coated substrate.
The release surface coated substrate of embodiment 1, wherein the binder is selected from at least one of polyimides, polyamides, polybenzimidazoles, polyamide-imides, polysulfones, polybismaleimides, liquid crystal polymers, polyethersulfone, polyphenylene sulfide, polybenzoxazine, epoxy resin, polyarylene etherketone, and combinations thereof.
The release surface coated substrate of any one of the previous embodiments, wherein the particles comprise an abrasive particle, a binder particle, and a fluoropolymer particle wherein the fluoropolymer particle comprises the first fluoropolymer.
The release surface coated substrate of any one of the embodiments 1-2, wherein the particles comprise an abrasive particle having an outer surface comprising the first fluoropolymer.
The release surface coated substrate of any one of the embodiments 1-2, wherein the particles comprise an abrasive particle having an outer surface comprising the binder.
The release surface coated substrate of any one of the embodiments 1-2, wherein the particles comprise an abrasive particle having an outer surface comprising the first fluoropolymer and the binder.
The release surface coated substrate of any one of the previous embodiments, wherein the abrasive particle is selected from silica, alumina, zirconia, barium titanate, calcium titanate, sodium titanate, titanium oxide, glass, biocompatible glass, diamond, silicon carbide, calcium phosphate, calcium carbonate, metallic powders, carbon fiber composites, polymeric composites, titanium, stainless steel, hardened steel, carbon steel chromium alloys, or any combination thereof.
The release surface coated substrate of any one of the previous embodiments, wherein the particles are delivered to the metal surface with a gas.
The release surface coated substrate of any one of the previous embodiments, wherein the first fluoropolymer has reactive groups selected from at least one of (a) —COX groups, wherein X is OH, ONa, OK, NH2, F, or Cl; (b) —S(═O)2X where X is OH, ONa, OK, NH2, F, or Cl; (c) —CH2OSO2Y where Y═OH, ONa, or OK; (d) —CH2OH; (e) phosphate group; and combinations thereof.
The release surface coated substrate of embodiment 9, wherein when the first fluoropolymer is a melt-processable fluoropolymer it comprises at least 30 reactive groups per 1,000,000 carbon atoms and when the first fluoropolymer is a non-melt processable fluoropolymer it comprises more than 5 reactive groups per 1,000,000 carbon atoms.
The release coated substrate of any one of the previous embodiments, wherein the first fluoropolymer is a PTFE homopolymer.
The release coated substrate of any one of the previous embodiments, wherein the metal substrate includes at least one of steel, high-carbon steel, stainless steel, aluminized steel, aluminum, and aluminum alloys.
The release coated substrate of any one of the previous embodiments, wherein the second fluoropolymer is a powder coating or a dispersion coating.
Advantages and embodiments of this disclosure are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. In these examples, all percentages, proportions and ratios are by weight unless otherwise indicated.
All materials are commercially available, for example from Sigma-Aldrich Chemical Company; Milwaukee, Wis., or known to those skilled in the art unless otherwise stated or apparent.
These abbreviations are used in the following examples: g=gram, min=minute, mm=millimeter, and wt=weight.
Cross Hatch Test
The adhesion of the coatings to the substrate was evaluated using the crosshatch test, in accordance with DIN EN ISO 2409. A crosshatch pattern of 1 mm was made in the coated substrates by using a knife. Adhesive tape (50 mm, available under the trade designation “TESA 4104” from Tesa SE, Hamburg, Germany) was applied as firmly as possible onto the cut lines. The adhesive tape was pulled vertically. After the tape was applied and pulled for 10 times, the appearance of the cut lines was evaluated according to DIN EN ISO 2409 (0=superior; 5=bad coating).
Endgroup Analysis
The number of carboxylic acid end groups per million carbon atoms of the fluoropolymers used was measured similar to the method described in U.S. Pat. No. 4,743,658 (Imbalzano et al.). The carboxylic acid end groups analyzed include carbonyl groups including carboxylic acid (COOH), carboxylate (COO−), carboxylic acid fluoride (COF), and carboxamides (CONH2). Sample material, which were thin films of fluoropolymer approximately 0.10 mm, were scanned on a Fourier-transform infrared spectrometer (available under the trade designation “NICOLET 510 FT-IR SPECTROPHOTOMER” from Thermo Electron Corp., Madison, Wis.). 16 scans were collected before the transform was performed, all other operational settings used were those provided as default settings in the system software. Similarly, a film of a reference material known to have none of the end groups to be analyzed was scanned. The reference absorbance spectrum was subtracted from the sample absorbance spectrum using the interactive subtraction mode of the software to obtain a difference spectrum. The CF2 overtone band at 2365 cm−1 was used to compensate for thickness differences between sample and reference films during the interactive subtraction. The difference spectrum represents the absorbances due to non-perfluorinated polymer end groups. The calibration factor (CF) used to calculate the numbers of carboxylic acid end groups per million carbon atoms was 440 for the absorbance at 3560 cm−1. The number of end groups per million carbon atoms was determined using the equation: carboxylic acid end groups per 1 million carbon atoms=absorbance×CF/film thickness of the sample material (in mm).
Cross-sectional Thickness Measurement
The cross-section thickness of the primer layer was tested using a coating thickness gauge (Mini Test 3100 available as from ElektroPhysik, Köln, Germany) with a non-ferrous sensor. The gauge was calibrated with a non-coated aluminum plate to establish zero thickness. About 5 points from the middle portion of the coated aluminum plates (Comparative Example and Example 1) were measured and the average was reported as the thickness of the primer layer.
600 g of abrasive particle was combined with 12 g of Fluoropolymer 1 and mixed in a tumbling mixer for 6 hours to coat the abrasive particles with the fluoropolymer.
The surface of an aluminum plate, used as received, was treated with the abrasive particles coated with Fluoropolymer 1 (from above) to form a coated plate. The coated abrasive particles were sprayed through a single nozzle at the surface of the aluminum plate using a pressure of 3.0 bar. The distance from the nozzle tip to the surface of the aluminum plate was 1.75 mm. The aluminum plate was moved so that the nozzle rastered the surface over 4.5-5 mm. The cross-sectional thickness of the primer layer (first fluoropolymer layer) was less than 5 micrometers.
The coated plate was air brushed for a few seconds with about 2 bar of air pressure to remove any abrasive particles, dust, and/or unattached fluoropolymer. The Topcoat was applied to the fluoropolymer coated surface of the aluminum plate by spray application at a pressure of 2 bar, using a spray gun (model 96 spray gun, Binks, Glendale Heights, Ill.), so as to obtain a dry coating thickness of about 20 micrometers. The coated multilayer article was then heated in an oven at 280° C. for 10 min to dry and then at 380° C. for 10 min to sinter.
The multilayer article was then tested on the exposed fluoropolymer layer following the Cross Hatch Test and received an appearance of a 4.
The same process as described in Comparative Example above was followed to make the multilayer article, except that Fluoropolymer 1 was blended with PES at a weight ratio of 1:1 and 12 g of this blend was combined with the abrasive particles. The amount of fluoropolymer on the abrasive particles was calculated to be 0.51 weight % and the cross-sectional thickness of the primer layer was less than 5 micrometers.
The multilayer article was tested on the exposed fluoropolymer layer following the Cross Hatch Test and received an appearance of a 0.
Foreseeable modifications and alterations of this invention will be apparent to those skilled in the art without departing from the scope and spirit of this invention. This invention should not be restricted to the embodiments that are set forth in this application for illustrative purposes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2016/025523 | 4/1/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62141344 | Apr 2015 | US |
