WO2009099574A1 - Mélanges polymères in situ à base de polysiloxane – matériaux d'amortissement pouvant être revêtus - Google Patents

Mélanges polymères in situ à base de polysiloxane – matériaux d'amortissement pouvant être revêtus Download PDF

Info

Publication number
WO2009099574A1
WO2009099574A1 PCT/US2009/000636 US2009000636W WO2009099574A1 WO 2009099574 A1 WO2009099574 A1 WO 2009099574A1 US 2009000636 W US2009000636 W US 2009000636W WO 2009099574 A1 WO2009099574 A1 WO 2009099574A1
Authority
WO
WIPO (PCT)
Prior art keywords
monomers
tie coat
polymer
coat
group
Prior art date
Application number
PCT/US2009/000636
Other languages
English (en)
Inventor
Joseph P. Morris
Atsuo Kondo
Original Assignee
Fujifilm Hunt Smart Surfaces, Llc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fujifilm Hunt Smart Surfaces, Llc filed Critical Fujifilm Hunt Smart Surfaces, Llc
Publication of WO2009099574A1 publication Critical patent/WO2009099574A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D151/085—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds on to polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
    • C08F283/122—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes on to saturated polysiloxanes containing hydrolysable groups, e.g. alkoxy-, thio-, hydroxy-
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/70—Siloxanes defined by use of the MDTQ nomenclature

Definitions

  • Cushioning material is useful to suppress vibration and noise as well as to absorb a shock for applications of automobile, building structure, house interior and exterior, roofing material, home electronics, electronics devise, sports equipment, sports facility, shoes and acoustical product.
  • existing cushioning materials such as rubber, resin and plastics etc. is mainly processed at factories to apply to objects.
  • users most likely have to cut desired shapes out of the sheet like commercial products. This procedure usually requires adhesives and detachment of the material is a common issue unless adhesion is sufficient. Slippage is another issue in case the material is placed under the heavy objects without adhesives. Also, it is difficult to apply materials to bent sites or narrow sites.
  • the present invention describes the preparation of stable polymer blend cushioning materials containing silicones. These blends may be used to form coatings that have good cushioning properties, vibration dampending and noise suppression
  • the invention encompasses a tie coat polymer blend cushioning material comprising at least one polysiloxane polymer and one organic polymer wherein said organic polymer is comprised of monomers that polymerize to single chain polymers and wherein said organic polymer is not comprised of crosslinking multifunctional monomers.
  • the tie coat polymer blend is comprised of polymers having typical weight-average molecular weights of from about 50,000 to about 500,000 and more preferably from about 120,000 to about 160,000.
  • the polysiloxane polymer of the tie coat polymer blend has the repeating unit formula
  • Ri and R 2 are independently substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted aryl, wherein said substituents, if present, are chosen from cyano, halogen or another group which does not provide another linking functionality.
  • At least one terminal end of the polysiloxane polymer has at a terminal reactive group; preferably the terminal reactive group is a hydroxyl group, an alkoxy group, an aryloxy group, an amino group, an amido group, a halogen, or a vinyl group; more preferably, the polysiloxane polymer is hydroxyl terminated dimethylsiloxane.
  • the tie coat polymer blend further comprises an organic monomer(s) capable of undergoing free radical polymerization in the presence of in- situ generated free radicals; preferably mono-olefinic monomers; more preferably ethylene monomers, propylene monomers, butene monomers, vinyl chloride monomers, vinyl fluoride monomers, fluoroacrylates, vinyl acetate monomers, styrene monomers, ring substituted styrene monomers, vinylpyrrolidine monomers, vinylnaphthalene monomers, N- vinylcabazole monomers, N-vinylpyrrolidone monomers, acrylic acid monomers, methacrylic acid monomers, acrylonitrile monomers, methacrylonitrile monomers, vinylidine fluoride monomers, vinylidine chloride monomers, acrolein monomers, methacrolein monomers, maleic anydride monomers, stilbene monomers, indene monomers, maleic acid monomers, or fumaric acid monomers.
  • the organic polymer is styrene, butylacrylate, other alkylacrylates or a mixture thereof.
  • the in-situ generated free radicals are initiated by the addition of benzoyl peroxide or di-t-butylperoxide, cumene hydroperoxide, and t-butyl hydroperoxide.
  • the tie coat polymer blend is comprised of further capable of being atomized and sprayed for application to a surface.
  • the tie coat polymer blend further comprises a silicone fluid capable of increasing the sprayability of the blend.
  • the tie coat polymer is further capable of forming an intimate covalent bond matrix with a surface to which it is applied.
  • the tie coat polymer blends have a viscosity of from about 40,000 to about 400,000 centipoise at about 25°C; preferably about 80,000 to about 250,000 centipoise at 25°C; and more preferably, about 95,000 to about 150,000 centipoise at 25 0 C.
  • the surface coat has a viscosity of about 8,000 to about 18,000 centipoise at 25°C; preferably about 9,000 to about 15,000 centipoise at 25°C; more preferably, about 10,000 to about 12,000 centipoise at 25 C C.
  • the curing agent of the tie coat polymer blend which further comprises a curing agent is not a tin-based catalyst, preferably N,N',N"- Tricyclohexyl-1 -methyl silanetriamine, platinum-based, or titanium-based catalysts, or other non-tin-based catalysts or organic-based catalysts, like crosslinker CA-40 (Wacker Chemie).
  • the invention encompasses a method for preparing a cushioning material composition comprising contacting an organopolysiloxane and one organic polymer wherein said organic polymer is comprised of monomers that polymerize to single chain polymers and wherein said organic polymer is not comprised of crosslinking multifunctional monomers.
  • the method further comprises contacting a free-radical initiator with the organopolysiloxane and/or organic monomer.
  • the free-radical initiator is an azo-bis-alkylnitrile; preferably AIBN. In other embodiments, the free-radical initiator is a peroxide; preferably benzoyl peroxide, di-t-butylperoxide, cumene hydrogenperoxide, or t-butyl hydrogen peroxide.
  • the polysiloxane polymer has the repeating unit formula
  • Ri and R 2 are independently substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted aryl, wherein said substituents, if present, are chosen from cyano, halogen or another group which does not provide another linking functionality.
  • At least one terminal end of the polysiloxane polymer has at a terminal reactive group; preferably the terminal reactive group is a hydroxyl group, an alkoxy group, an aryloxy group, an amino group, an amido group, a halogen, or a vinyl group; more preferably, the polysiloxane polymer is hydroxyl terminated polydimethylsiloxane.
  • the hydroxyl terminated polydimethylsiloxane has viscosity of less than 100 centistokes at 25 0 C.
  • the hydroxyl terminated polydimethylsiloxane has viscosity between 2000 to 8000 centistokes at 25 °C.
  • the hydroxyl terminated polydimethylsiloxane has viscosity between 10,000 to 50,000 centistokes at 25 0 C.
  • the tie coat polymer blend further comprises an organic monomer(s) capable of undergoing free radical polymerization in the presence of in- situ generated free radicals; preferably mono-olefinic monomers; more preferably ethylene monomers, propylene monomers, butene monomers, vinyl chloride monomers, vinyl fluoride monomers, fluoroacrylates, vinyl acetate monomers, styrene monomers, ring substituted styrene monomers, vinylpyrrolidine monomers, vinylnaphthalene monomers, N- vinylcabazole monomers, N-vinylpyrrolidone monomers, acrylic acid monomers, methacrylic acid monomers, acrylonitrile monomers, methacrylonitrile monomers, vinylidine fluoride monomers, vinylidine chloride monomers, acrolein monomers, methacrolein monomers, maleic anydride monomers, stilbene monomers, indene monomers, maleic acid monomers, or fumaric acid monomers.
  • the organic polymer is comprised of styrene, butyl acryl ate, other alkylacrylates or a mixture thereof.
  • the polymers of the method have typical weight- average molecular weights of from about 80,000 to about 250,000 and more preferably from about 120,000 to about 160,000.
  • the method is performed in a nitrogen sparged atmosphere.
  • the method further comprises contacting with a bifunctional tethering agent;
  • a bifunctional tethering agent comprises a primary and/or secondary amine functionality and a siloxane-like functionality.
  • the initiator of the method is introduced to the organopolysiloxane and/or organic monomer in a plurality of doses. In another embodiment, the initiator of the method is introduced to the organopolysiloxane and/or organic monomer in a single dose. In another embodiment, the method farther comprises contacting with a curing agent, wherein said curing agent is not a tin-based catalyst.
  • the shear rates contemplated during polymerization to form the tie coat polymer blend is typically in the range of from about 10 min "1 to about 1,500 min "1 , and more preferably from about 100 min "1 to about 1,000 min "1 .
  • the product produced by the method does not possess elongated microphase separated polymer morphology.
  • the method further comprising addition of water.
  • the invention encompasses a cushioning material product made by the process of contacting an organopolysiloxane and one organic polymer wherein said organic polymer is comprised of monomers that polymerize to single chain polymers and wherein said organic polymer is not comprised of crosslinking multifunctional monomers.
  • the product is made by a process that further comprises contacting a free-radical initiator with the organopolysiloxane and/or organic monomer. In another embodiment, the product is made by a process in which the contacting is performed in a nitrogen sparged atmosphere.
  • the product is made by a process which further comprises the addition of water.
  • the invention provides a method of cushioning a surface comprising the step of contacting a surface with the cushioning material composition of the invention.
  • the cushioning is vibration suppression or noise suppression.
  • vibration suppression refers to reducing the impact of vibration energy on surfaces or substrates coated with the invention. This impact includes damage to the substrate or structure, fatigue of the substrate or structure, and transmission of vibration through or from the substrate or structure.
  • noise suppression refers to reducing the transmission and/or the reflection of noise energy through or reflected from a surface or substrate coated with the invention.
  • crosslinking multifunctional monomers refers to monomers which are capable of forming a crosslinked polymer chain when homopolymerized.
  • halogen refers to fluorine, chlorine, bromine or iodine.
  • alkyl refers to a straight-chained or branched hydrocarbon group containing 1 to 50 carbon atoms.
  • alkyl groups include, but are not limited to methyl, ethyl, n-propyl, isopropyl, tert-butyl, and n-pentyl. Alkyl groups may be optionally substituted with one or more substituents.
  • C1-C3 alkyl refers to a straight or branched hydrocarbon chain radical, containing solely carbon and hydrogen atoms, having in the range from one up to three carbon atoms, and which is attached to the rest of the molecule by a single bond, such as illustratively, methyl, ethyl, n-propyl, and 1-methylethyl (iso-propyl).
  • aryl refers to a hydrocarbon monocyclic, bicyclic or tricyclic aromatic ring system.
  • Aryl groups may be optionally substituted with one or more substituents. In one embodiment, 0, 1, 2, 3, 4, 5 or 6 atoms of each ring of an aryl group may be substituted by a substituent. Examples of aryl groups include phenyl, naphthyl, anthracenyl, fluorenyl, indenyl, azulenyl, and the like. Additionally, the term “aryl” refers to a hydrocarbon monocyclic, bicyclic or tricyclic bridged ring systems wherein at least one rings is aromatic.
  • alkoxy refers to an -O-alkyl radical.
  • aryloxy refers to an -O-aryl radical.
  • An “amido” is an -C(O)NH 2 .
  • substituted means that a hydrogen radical on a compound or group (such as, for example, alkyl, alkenyl, alkynyl, alkylene, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, cyclyl, heterocycloalkyl, or heterocyclyl group) is replaced with any desired group that does not substantially adversely affect the stability of the compound.
  • a hydrogen radical on a compound or group such as, for example, alkyl, alkenyl, alkynyl, alkylene, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, cyclyl, heterocycloalkyl, or heterocyclyl group
  • substituents include, but are not limited to, halogen (F, Cl, Br, or I), hydroxyl, amino, alkylamino, arylamino, dialkylamino, diarylamino, alkylarylamino, cyano, nitro, mercapto, thio, imino, formyl, carbamido, carbamyl, carboxyl, thioureido, thiocyanato, sulfoamido, sulfonylalkyl, sulfonylaryl, alkyl, alkenyl, alkoxy, mercaptoalkoxy, aryl, heteroaryl, cyclyl, heterocyclyl, wherein alkyl, alkenyl, alkyloxy, alkoxyalkyl, aryl, heteroaryl, cyclyl, and heterocyclyl are optionally substituted with alkyl, aryl, heteroaryl, halogen, hydroxyl, amino, mer
  • terminal reactive group refers to a group bound to the terminal end of a polysiloxane polymer which is further capable of undergoing a chemical reaction with another compound or nearby reactive group.
  • Terminal reactive groups include, but are not limited to, a hydroxyl group, an alkoxy group, an aryloxy group, an amino group, an amido group, a halogen, or a vinyl group.
  • organic monomer(s) capable of undergoing free radical polymerization in the presence of in-situ generated free radicals refers to a polymer made of organic monomers which are capable of forming a polymer through reaction with radicals generated by the monomers themselves rather than by reaction with external free radical generators.
  • Mono-olefinic refers to a monomoer having only one reactive carbon-carbon double bond. Regarding the inveniton, one reactive carbon-carbon double bond is actually difunctional since it can bond to two neighboring monomers.
  • Mono-olefinic monomers include, but are not limited to, ethylene monomers, propylene monomers, butylene monomers, vinyl chloride monomers, vinyl fluoride monomers, fluoroacrylates, vinyl acetate monomers, styrene monomers, ring substituted styrene monomers, vinylpyridine monomers, vinylnaphthalene monomers, N-vinylcabazole monomers, N-vinylpyrrolidone monomers, acrylic acid monomers, methacrylic acid monomers, acrylonitrile monomers, methacrylonitrile monomers, vinylidine fluoride monomers, vinylidine chloride monomers, acrolein monomers, methacrolein monomers, maleic anydride monomers, stilbene monomers
  • bifunctional tethering agent refers to a compound or compounds used to form a molecular bridge through covalent bonding, between a tie coat and an epoxy layer.
  • the bifunctional tethering agent comprises a combination of primary and/or secondary amine functionality and a siloxane-like functionality.
  • siloxane-like functionality refers to, typically, triethoxysilane and trimethoxysilane.
  • elongated morphology refers to having morphological features in the phase separated or microphase separated material that are rod-like or needle-like.
  • Silicone fluid refers to a silicone based liquid or flowable material which, when added to a polymer, reduces the viscosity and increases the ability of said polymer to be sprayed onto a surface by a forced spray nozzle, and also improves the fouling release properties. Silicone fluids include, but are not limited to SF69 and SFl 147.
  • curing agent refers to an organic or inorganic catalyst or other material which is capable of curing the tie coat resin by reaction with terminal Si-OH groups.
  • Curing agents include but are not limited to N,N',N" Tricyclohexyl-1 -methyl silanetriamine, tin based catalysts, platinum based catalyst, or other non-tin based catalysts.
  • anticorrosive epoxy layer refers to a thermosetting polymer, that cures by the reaction of epoxide and amine functionatilities, that provides corrosion protection for metal, concrete barriers, or water incursion barriers, and may be further used as a primer to improve the adhesion of marine paints especially on metal surfaces where corrosion (rusting) resistance is important.
  • substrate and “surface” are herein used interchangeably and refer to various surfaces, including but not limited to plastics, resin, wood, glass, concrete, and metals (iron, aluminum).
  • release oil refers to a material which, when incorporated into a polymer resin or silicone surface material slowly diffuses over time, or stays at the surface, thereby increasing fouling release properties for the material. Release oils include, but are not limited to low molecular weight silicone based oils, SFl 147, SFl 154, DMSC 15, and DBE 224.
  • the tie coat compositions of the invention contain monomers that polymerize to single chain polymers and do not contain crosslinking multifunctional monomers.
  • Such tie coats are stable graft polymers and copolymers which are comprised of a polymer blend (stabilized by graft copolymers) rather than a simple graft polymer.
  • the tie coats of the invention do not possess elongated morphologies that have been previously disclosed (see, e.g., US 5,449,553 and US 5,593,732).
  • the tie coats of the invention do not require high shear for high toughness morphologies and only require sufficient shear to achieve a homogenous mixture of starting materials for polymerization.
  • What is observed in the tie coat formulations are small spheroid particle morphologies (observed by electron micrographs) that achieve equivalent or better levels of toughness to absorb mechanical insult during ship operation and other abrasive environments, and imparts this toughness to surface coat by chemical bonding between surface and tie coat (silicon, butyl acrylate and polystyrene - block co-polymer).
  • the tie coat forms an intimate covalent matrix to impart a toughness to the silicon surface coat and increases the cushioning, vibration suppression and noise suppression properties of the silicon top coat.
  • the tie coat provides cushioning, vibration suppression and/or noise suppression properites via energy absorption.
  • the tie coat when the tie coat is applied to a substrate, the tie coat wll provide cushioning, vibration suppression and/or noise suppression properties to such substrate.
  • the tie coat when the tie coat is used adjacent a substrate or introduced into a compartment, it will provide cushioning, vibration suppression and/or noise suppression properites to the substrate or the compartment.
  • the tie coat when formed into an intimate covalent matrix, it imparts a toughness to the silicon surface coat and increases the cushioning, vibration suppression and/or noise suppression properties of the silicon top coat.
  • tie coats of the invention include the following: 1.
  • the samples for comparison example were cut out from the purchased product.
  • the sheet material of the tie coat can be easily prepared with the procedure described below.
  • a stainless mold form of 150 mm square is placed on a pan made of polypropylene or polyethylene.
  • Loss Coefficient value is 0.329 at 23 ⁇ 2°C at 15Hz and it exceeds 0.2, which the industrial standard stipulates as material with excellent vibration absorbing effect.
  • the anticorrosive epoxy layer further comprises a silane coupling agent having amines, such as primary and/or secondary amines.
  • a silane coupling agent having amines such as primary and/or secondary amines.
  • SCM 501C a compound known as SCM 501C is added to an epoxy layer (if more than one epoxy layer is used, then the SCM 501 C is added to the outermost or last applied layer). See U.S. Patent No. 6,391 ,464, entitled Epoxy Coatings and Surfaces Coated Therewith. We have subsequently discovered that several other reagents will improve this bond via silicone- to-silicone bonding while using substantially less material reagent.
  • These new reagents include but are not limited to: methylaminopropyltrimethoxysilane, N- phenylaminopropyltrimethoxysilane, and cyclohexylaminopropyltrimethoxysilane.
  • the tie coat has a silicone fluid incorporated into the final product that allows a much easier spray application.
  • This fluid can be incorporated at a volume of approximately 1% to about 30%, and in certain embodiments 15%.
  • the tie coat is bonded to a surface coat.
  • the tie coat of the invention bonds to a surface coat through silicone cross linking between the tie coat and surface coat. This bond is covalent in nature and very strong. The nature of this bond creates a "oneness" between the two layers. This "oneness" results in a transmission of toughness to the surface coat from the tie coat and allows the entire system to achieve a toughness that is not present in traditional silicone coatings.
  • the surface coat has this toughness which provides a much more resilient surface compared to standard silicone fouling release materials while maintaining the fouling release characteristics required. This results in a coating that is superior in damage resistance, debonding resistance, and longevity.
  • the invention provides a tie coat bonded to epoxy.
  • the tie coat bonds to the epoxy in both physical/mechanical as well as chemical means.
  • a bifunctional tethering agent is added that contains an amine functionality at one end of the molecule with a siloxane-like functionality at the other end. Since silicones form low energy surfaces, some of the siloxane functionality rises to the surface (herein referred to as "self-assembling") of the epoxy preparing to bond with the tie coat silicone functionalities.
  • the amine functionality bonds to the epoxide functionality in the epoxy layer while the silicone molecules that self-assemble at the air-surface side of the epoxy layer bind to silicone molecules in the Tie Coat.
  • bifunctional tethering agents contemplated by the present invention include SCM 501 C, aminopropyltriethoxysilane, aminopropyltrimethoxysilane, methylaminopropyltrimethoxysilane and cyclohexylaminopropyltrimethoxysilane. See Table 1 below.
  • tie coat bonded to epoxy which is bonded to a substrate and a top coat bonded to a tie coat bonded to epoxy bonded to a substrate.
  • the polysiloxanes used in this process are polymers that conform to the general repeating unit formula
  • Riand R 2 are organic groups, especially alkyl groups of 1-3 carbon atoms which may be substituted and which may be the same or different and in the simplest case they are methyl groups (poly(dimethylsiloxane), PDMS).
  • the Ri and R 2 groups may also be other monovalent alkyl or aryl radicals or they may be substituted, for example with halogen substitutents or with cyano groups.
  • the ends of the polysiloxane chains bear terminal reactive groups, such as hydroxyl, alkoxy, aryloxy, amino, amido, halo, and vinyl.
  • terminal groups are used in setting or curing of the polysiloxane blends and/or in bonding the layer containing these structures to a polysiloxane topcoat such as RTVl 1 or a tethering agent.
  • a polysiloxane topcoat such as RTVl 1 or a tethering agent.
  • An example of suitable end-functionalized polysiloxanes that are useful in forming the stable polymer blends of this invention are hydroxyl-terminated silicone fluids.
  • the viscosities of useful fluids may range from about 500 to 50,000 cps and more preferably from 1,000 to 20,000 cps at 25 0 C.
  • the free radically polymerizable monomers may be any polymerizable mono-olefinic monomer such as ethylene, propylene, butene, vinyl chloride, vinyl fluoride, vinyl acetate, styrene, ring substituted styrenes, vinylpyridine, vinylnaphthalene, N-vinylcarbazole, N-vinylpyrrolidone, acrylic acid and methacrylic acid, their derivatives including salts, esters, and amides, acrylonitrile, methacrylonitrile, vinylidine fluoride, vinylidene chloride, acrolein, methacrolein, maleic anhydride, stilbene, indene, maleic and fumaric acids and their derivatives, and conjugated dienes such as butadiene and isoprene.
  • polymerizable mono-olefinic monomer such as ethylene, propylene, butene, vinyl chloride, vinyl fluoride, vinyl acetate, styren
  • the monomers may include fluoriated analogs of the monomers provided supra. These monomers may be polymerized singly, or in combinations of two or more, in the presence of the polysiloxane and a free radical source. While polyfunctional "crosslinking monomers" such as divinylbenzene, ethylene glycol dimethacrylate, trimethylolpropane trimethacrylate, pentaerythritol tetramethacrylate, etc., may be used in the present invention in very small amounts ( ⁇ about 5% and most preferable ⁇ 1 % based on the weight of the mono-olefinic monomer(s)), the use of only monomers containing a single polymerizable olefinic group is preferred in order to avoid gelation while allowing the free radical initiator to be added to the reactants in a single batch in a one-pot process.
  • polyfunctional "crosslinking monomers” such as divinylbenzene, ethylene glycol dimethacrylate, trimethylolpropan
  • the proportion of organopolysiloxane used may be varied within wide limits but is preferably 25 to 60% by weight of the reactants.
  • the free radical initiation process may involve common free radical initiators such as peroxides or azobisisobutyronitrile (AIBN), redox initiators, photoinitiators, or the creation of radicals through thermal treatment or use of ionizing radiation.
  • free radical initiators such as peroxides or azobisisobutyronitrile (AIBN), redox initiators, photoinitiators, or the creation of radicals through thermal treatment or use of ionizing radiation.
  • the preferred initiators are peroxides and hydroperoxides of the formula ROOR, ROOH, and RCOOOR, (wherein each R is independently alkyl or aryl) such as benzoyl peroxide, t-butyl hydroperoxide, dicumyl peroxide, t-butyl perbenzoate, and the like, as well as AIBN.
  • the amount of free radical initiator used will typically be in the range of 0.005% to 2% based on the combined weight of organopolysiloxane and monomer. Generally a single initiator will be used, although two or more initiators may be employed. Generally the initiator is added in a single batch at the start of the polymerization process, although it is possible to add the initiator in increments.
  • the temperature for the free radical polymerization is not critical but should be varied to generate a suitable temperature for decomposition of the initiator chosen. Generally this temperature is in the range of 50 - 150 °C.
  • the free radical polymerization is preferentially carried out with stirring under an inert atmosphere in the presence of a liquid that boils in the range of 50 - 150 0 C.
  • This liquid should have a low chain transfer constant, limiting its participation in the chemical reactions that are occurring.
  • water may be used for this purpose even though it does not dissolve polysiloxanes or most vinyl monomers.
  • crosslinking is required to generate stable polymer blends of the "interpenetrating polymer network” type.
  • stable we mean polymer blends that will not de-mix on storage.
  • This explains the use of a "polyfunctional (crosslinking) monomer” by Griffith (US Patent # 5,449,553, the contents of which are incorporated by reference) in the preparation of similar organopolysiloxane-based release layers.
  • non-crosslinked polymer blends that are stabilized by in-situ generated graft copolymers that serve as macromolecular surfactants for stabilizing the mixture of the pre-formed polysiloxane and the free radically produced polymer.
  • the free radicals that are generated may create graft copolymers composed of a polysiloxane backbone and side chains of the free radically polymerized monomer(s) by chain transfer to polysiloxane.
  • the product of the free radical process is clearly a polymer blend rather than phase separated graft copolymer as evidenced by the micrometer length scale of phase separation.
  • Graft copolymers microphase separate on the scale of a few to a hundred nanometers, while polymer blends, even when stabilized by copolymer surfactants, exhibit phase separation on the micron scale or larger.
  • the opaque (white) appearance of the products of the process reported herein provides strong evidence of creation of polymer blend on a micrometer length scale which is thus able to scatter light rather than a graft copolymer as the dominant product.
  • a surprising aspect of the present invention is the long term stability of the novel polymer blends in the absence of crosslinking.
  • Blends of incompatible polymers phase separate on storage and addition of block copolymers is usually rather inefficient in stabilizing them since most of the added block copolymer forms micelles.
  • the generated polymer blends are completely soluble in suitable solvents, indicating that no crosslinking is present, and they have been stored for periods of > 2 years without any indication of macroscopic phase separation.
  • the tie coat imparts mechanical strength and toughness to a top coat due to its chemical structure, physical properties and morphology.
  • tie coat includes a hydroxy-terminated poly(dimethylsiloxane) that is partially grafted with a random copolymer of n-butylacryate and styrene. Such a structure is shown below:
  • Exemplified components of the tie coat are graft copolymers with polydimethylsiloxane (PDMS) backbones and grafted chains of a poly(styrene-co-n-butyl acrylate).
  • PDMS polydimethylsiloxane
  • the chemical species provides covalent bonds between silicone functionalities and styrene/acrylic polymer groups, and the graft copolymer acts to stabilize and prevent different components in the tie coat from undergoing macroscopic phase separation.
  • the free hydroxyl groups allow bonding to both the silicone rubber top coat and to the the epoxy substrate, as well as the tethering agent.
  • the free hydroxyl groups are allowed to react with a silane coupling agent that is added into the epoxy protective coating, providing strong adhesion between the epoxy base coat and the tie coat. Further, the hydroxyl groups are capable of reacting and linking into a crosslinked network of the top coat. Such bonding allows for efficiency of stress transfer between the two layers and strengthens the material.
  • the glass transition temperature T g of the silicone rubber surface coat ranges from about -150 0 C to about -60 0 C, preferably around -120 0 C, resulting in a soft surface coat.
  • the tie coats of the invention contain styrene based polymers, such as poly(styrene-co-n-butylacrylate) copolymer, having about 75 wt% n-butylacrylate, which has a much higher Tg, ranging from about about -50 °C to about 0 0 C, preferably around -20 0 C.
  • the higher glass transition temperature provides a toughening of the material, which allows the material to absorb the mechanical energy of impacts and scrapes.
  • the silicone functionality which is bonded to the tie coat maximizes the transfer of mechanical energy from the weaker top coat into the tie coat where it is absorbed and dissipated.
  • Another aspect of the invention is a monoplex system that enhances the bonding of the cushioning material here to underlying substrates.
  • the monoplex system comprises a unique formulation of tie coat and surface coat chemistries that "self assembles.” This monoplex systems, when assembled and cured, provides a smooth polysiloxane RTV-like surface coat.
  • the mixed layer of the Monoplex system assembles itself to have the tie coat and top surface functionality that it needs within the single applied layer. Once applied to the surface the top coat components rise toward the surface and the tie coat components move down toward the underlying epoxy.
  • the Monoplex system does not have well defined layers even after this self assembly process has occurred during cure. The bottom is richer in the tie coat material and top is richer in the surface coat material and there is a gradual change in composition from layer bottom to layer top (self-assembly). This self-assembling release coating allows greater ease of application and maintenance.
  • the Monoplex system comprises an anticorrosive epoxy layer applied to a substrate, and a monoplex layer applied to said anticorrosive epoxy layer comprising a blend of silicone surface coat material and a tie coat material.
  • the anticorrosive epoxy layer further comprises a silane coupling agent having amines, such as primary and secondaty amines.
  • a silane coupling agent having amines such as primary and secondaty amines.
  • SCM 501 C is added to the epoxy layer (if more than one epoxy layer is used, then the 501C is added to the outermost or last applied layer). See U.S. Patent No. 6,391,464, entitled Epoxy Coatings and Surfaces Coated Therewith We have subsequently discovered that several other reagents will improve this bond while using substantially less material reagent.
  • These new reagents include but are not limited to: methylaminopropyltrimethoxysilane, N- phenylaminopropyltrimethoxysilane, and cyclohexylaminopropyltrimethoxysilane.
  • the amount of tie coat resin, incorporated in the blend with surface coat resin is between 5% and 99%, or preferably between 50% and 99%, and most preferably between 75% and 95%.
  • the amount of surface coat resin incorporated into the blended single layer is between 1% and 95%, or preferably between 1% and 50%, and most preferably between 5% and 25%.
  • the amount of tie coat resin is around 85%, and the amount of surface coat is around 15%.
  • Release oils may be incorporated into the monoplex system in a similar fashion to their incorporation in the surface coat of the duplex system. Release oils include SFl 147, SFl 154, DMSC 15 and DBE224.
  • a silicone fluid is added to aid the sprayability of the monoplex coating.
  • the silicone fluid is selected from SF69 and SFl 147.
  • the tie coat polymer blend is modified to incorporate a perfluorinated acrylate or methacrylate (or some other fluorinated monomer).
  • a perfluorinated acrylate or methacrylate or some other fluorinated monomer.
  • Another aspect of the invention is a duplex system that enhances the bonding of the cushioning material compositions to underlying substrates.
  • a compound known as SCM 501C is added to the second epoxy layer (if only one epoxy layer is used, then the 501C is added here). See U.S. Patent No. 6,391,464, entitled Epoxy Coatings and Surfaces Coated Therewith. We have subsequently discovered that several other reagents will improve this bond while using substantially less material reagent. These new reagents include but are not limited to methylaminopropyltrimethoxysilane, N-phenylaminopropyltrimethoxysilane, and cyclohexylaminopropyltrimethoxysilane.
  • these reagents act by a unique mechanism whereby: 1. Due to the silane function, the reagents will bloom to the surface of the epoxy thereby exposing the silane functionality for covalent bonding to the tie coat. In certain embodiments, the blooming occurs in the epoxy later, wherein the need for polyfunctional reagents has been eliminated. Epoxies are crosslinked. 2. The amine function binds covalently to the epoxide functionality of the epoxy layer. 3. These reagents can be present at as low a concentration as 1 % or less and achieve a tight bond. We have tested them at concentrations as high as 30% with good results however, the lower concentration of 1% provides a significant cost advantage.
  • the tie coat bonds very strongly when applied to glass-filled fiberglass or vinyl ester. No coupling agent, epoxy layer, or surface treatment is required. This could be extended to other surfaces, e.g. polyurethanes or acrylics, etc.).
  • Duplex System can, in some aspects, be applied directly to a substrate without the presence of an anticorrosive epoxy layer.
  • the adhesion of the tie coat is at least as good as its adhesion to the second epoxy later with the tethering agent in it, in the standard duplex system.
  • the duplex system is particularly well suited for application to small pipes such as pipes used in irrigation, fire suppression, water transport in buildings, and other similar uses; roofing; wind Turbines/windmills; aircraft; wiring (high tension electrical wires, telephone wires, electrical conduit wires); buildings and foundations (salt erosion inhibitor); power Plant Efficiency; dock surfaces; oil Rigs ( Fouling induced requirement to "overbuild” the strength of the pilings); "anti-ice” applications including, roofs, windmills, aircraft wings, ship and oil rig railings and non-step surfaces (wherever deice or de-snow is used).
  • compositions herein posses desirable spray characteristics that balance sprayability with achieving coating thickness. Viscosities in the region of 18,000 centipoise are more difficult to spray and require the addition of large amounts of solvent to achieve sprayability. When large quantities of solvent are used, it is difficult to achieve the required coating thickness (build) and the additional solvent creates a regulatory compliance problem due to the level of volatile organic solvent (VOC).
  • VOC volatile organic solvent
  • the compositions herein provide enhanced ability to apply the surface coat to large installations and to achieve the required thickness. This makes the Duplex System and Monoplex System very user friendly and results in a much more consistent application process.
  • Suitable combinations of tethering agent used in the second epoxy layer include, but are not limited to, those listed in Table 1 below.
  • Tie coats previously disclosed are manufactured having an elongated morphology which is produced using high shear rates in a reaction vessel. It is found that elongated morphologies of tie coats are not required to achieve a tie coat which provides comparable or equivalent levels of strength and durability. The resulting method of manufacture is simpler than that previously disclosed and results in a reduction in cost and manufacturing burdens. The resulting morphology is not elongated and provides for greater stability.
  • water is used to remove heat during tie coat synthesis.
  • the process for the production of the tie coat results in an exotherm as heat is developed in the reaction.
  • There are several ways to control the evolving heat including the presence of a solvent or the presence of a non-miscible fluid.
  • Two properties of water are ideal for this process. The first is water's boiling point of 100 0 C. We wished to maintain the temperature of the reactor at near 100 0 C for the purpose of achieving full reaction without overheating the developing polymer. Additionally, we wished to use a coolant fluid that would be environmentally benign as well as inexpensive. We found that water worked extremely well in controlling the reaction and the reactor. Following the completion of the reaction, the majority of the water is decanted and then the material is heated to 100 0 C to drive off the remaining water.
  • a radial initiator such as benzoyl peroxide
  • a radial initiator was utilized for grafting reactions.
  • an initiator to a reaction mixture: (i) gradual addition of initiator - Typically this method is used to achieve close control of the reaction, but this requires careful monitoring and equipment to meter in the exact amount of initiator over time during the progress of the reaction; and (ii) initiator added all at once - this method of initiator addition can result in a less well controlled reaction with less well controlled polymer chain length and consistence. However this is an easier method for large scale manufacturing.
  • the tie coats of the invention may be bonded to a surface wherein the covalent bonding between silicone polymer backbones and hydrocarbon polymer grafts in the tie coat is key to the reactive compatibilization of the polymer blend.
  • a silane coupling agent is used to bond the epoxy layer to the tie coat.
  • An example of a silane coupling agent is SCM 501 C (Momentive Performance Materials), which has primary amine groups that bond to epoxide groups in the epoxy coat and which has silicone functionalities that bond to silicone end groups (hydroxyls) in the tie coat. Additionally, the Si-OH groups in the tie coat bond to silicone end groups in the surface coat to affect bonding between the layers.
  • a release oil is physically mixed into the surface coat, and slowly diffuses out over time.
  • Release oils include SFl 147, SFl 154, DMSC 15 and DBE224.
  • the surface coat surface tension is very low; about 20-25 dyne/cm.
  • the coat thickness ranges from about 8 to about 16 mil, preferably from about 10 to about 14 mil.
  • a silicone fluid is added to aid the sprayability of the tie coat.
  • the silicone fluid is selected from SF69 and SFl 147.
  • the viscosity of the resin determines the extent of how well the paint will spray.
  • the viscosity of the surface coat silicone significantly improved spray characteristics when the viscosity was reduced to 10,000 to 12,000 centipoise. Viscosities in the region of 18,000 centipoise were more difficult to spray and required the addition of large amounts of solvent to achieve sprayability. When large quantities of solvent were used, it was difficult to achieve the required coating thickness (build) and the additional solvent creates a regulatory compliance problem due to the level of volatile organic solvent (VOC). This discovery provided the enhanced ability to apply the surface coat to large installations and to achieve the required thickness.
  • the coatings of the present invention provide for self-assembly of the silicone moieties when free of cross linkers in the tie coat.
  • the epoxy layer that serves as the substrate for the tie coat contains a coupling agent such as SCM 501 C, which contains both amine and siloxane functionality, as discussed above.
  • SCM 501 C is mixed with the epoxy and coated on a substrate, there is a tendency, due to the low energy of silicone surfaces, for some of the silicone moieties in the mixture to migrate to the surface, while the amine groups bond to epoxy functionality in the mixture.
  • silicone groups at the surface of this epoxy layer can then form chemical bonds with some of the -Si-OH groups present in the tie coat formulation. This provides for strong interfacial bonding between the epoxy layer and the tie coat layer. While some of the silicone functionality in the tie coat layer reacts with the tethering agent on the surface of the epoxy layer, we have evidence (XPS experiments reveal that the tie coat surface is rich in silicones) that there is also a tendency for self-assembly (migration of silicone to the surface) during curing of the tie coat layer.
  • silicone moieties in the Tie Coats and the Epoxy Coats formulated with Tethering Agents in accordance with the present invention have a tendency to self-assemble to the air-surface side of the coats to (a) decrease surface energy and interfacial tension between the layers as they are applied and (b) form chemical bonds between silicone functionality of the tethering agents and of the tie coat.
  • the Epoxy Coat binding to the Tie Coat is no-longer limited to simply overt assembly in which hydrocarbon bonding and Van der Waals intermolecular attractions occur, but also uniquely includes silicone-to-silicone bonding between the Epoxy Coats containing Tethering Agents and the Tie Coats and between the Tie Coats and the Surface Coats due to this self-assembling feature in accordance with the present invention.
  • the coatings or composites of the present invention are low surface energy coatings and include a silicone polymer matrix having natural free volume therein in which silicone oil is present and will very slowly diffuse out therefrom due to the slight gradient at the air-surface side of the Surface Coat.
  • the coatings or composites of the present invention can be infused with effective amounts of antifouling, antialgae, antibacterial (bacterialcidal and bacteriostatic), antibiofilm-forming, biocidal, biostatic and other like agents (antifoulants), such as those disclosed in U.S. Patent No. 7,087,106 entitled Materials and Methods for Inhibiting Fouling of Surfaces Exposed to Aquatic Environments, U.S. Patent No. 5,314,932 entitled Antifouling Coating and Method for Using Same, U.S. Patent No.
  • Poseidon Ocean Sciences Inc's Natural Bioproducts (NB) including Poseidon's NBl 7 and NB 16 compounds as reported in Life on the Ocean, Life on the Ocean Wave, Dr. Jonathan R. Matias, CEO, Poseidon Ocean Sciences Inc., http://www.poseidonsciences.com/oceanwave_ppcj.html, Rittschof, D. 1999, Fouling and natural product antifoulants.
  • compositions of the invention possess superior ease of application properties.
  • the compositions can be applied by spray methods as they spray as easily as traditional epoxy paints.
  • the compositions of the invention more easily atomizes during the spraying process resulting in a more uniform spray application and an improved ability to achieve the required build thickness.
  • Tether agents give an expanded time window for subsequent application of tie coat, ranging from 24 hrs to longer, thus providing application options.
  • An additional advantage includes not requiring a reactivation by spraying an "activating" coat of epoxy or other epoxy mist coats. Cure times
  • compositions of the invention are capable of being layered upon each layer achieving a "dry tack" stage, assessed, for example, by pressing the back of a finger onto the epoxy and removing the finger with no epoxy paint adhering to the finger.
  • each layer may be cured for up to several days prior to application of a second layer. In most cases, composion layers are allowed to cure within 24 hours of application.
  • compositions of the invention can be applied at varying thicknesses.
  • Each coat may be applied by hand or or by using airless or other appropriate spraying equipment and applied according to the preference of the applicator.
  • each coat will be applied at a wet-film thickness of about 2 to about 30 mils, preferrably about 4 to about 25 mils, more preferably about 6 to about 20 mils.
  • the epoxy layers are generally applied at a well-film thickness of about 2 to about 12 mils, preferably about 4 to about 10 mils, more preferably about 6 to about 9 mils.
  • Fouling release tie coat and surface coat layers are generally applied at a wet-film thickness of about 10 to about 30 mils, preferably about 13 to about 25 mils, more preferably about 16 to about 20 mils.
  • the tie coat will be applied at a wet-film thickness of from about 12 to about 14 mils and the surface coat will be applied at a wet-film thickness of from about 16 to about 20 mils.
  • the tie coat can have thickness of about 2 to about 6000 or more mils depending upon the application (e.g., shoe paddings, door insulations, roof coatings, boat or ship hulls, airplane fuselages, automobile bodies, motor houses, athletic equipment, namely football, hockey and lacrosse equipment, submarine hulls, and sound isolation or quiet chambers, to name a few).
  • the invention enables either industries or home users to easily and safely prepare excellent cushioning material, the tie coat by mixing two parts solution.
  • Mixed solution can be applied to various substrates such as plastics, resin, wood, glass, concrete, iron and aluminum etc. for any thickness either by hand or spray.
  • the tie coat cures at room temperature and imparts excellent vibration and noise suppression or shock absorption to anywhere it is applied. Desired shape is available in case mixed solution is cured using mold forms. Examples
  • Molecular weights and polydispersities of the tie coat were determined by SEC/GPC in tetrahydrofuran at 30 0 C, using tetrahydrofuran as the mobile hase. Calibration wsw carried out using linear polystyrenes as standards.
  • Viscosity of the tie coat resin was measured using a Brookfield RTV viscometer and large spindles.
  • Polymers of the invention can be identified using physical appearance such as color and transparency.
  • physical appearance such as color and transparency.
  • One of skill in the art will readily be able to recognize differences in physical appearance between samples and standards and will be able to apply this information for identification purposes.
  • Elemental analysis was carried out by Galbraith Laboratories, Knoxville, TN.
  • Peel tests provide a measure of the strength (energy) of adhesion between the various layers in the system. They are described here for measuring the strength of adhesion between different layers.
  • a five inch wide strip of nylon mesh (type used for dry wall) was imbedded at the interface between a second layer and the tie coat, by placing the mesh on the tacky layer and then painting the tie coat over top of it. An eight inch length of the mesh strip was left protruding from the interface and over the edge of the tile form gripping in the pull tests.
  • the tile is clamped to the base of an Instron tensile testing machine and the strip of mesh, reinforced with duct tape and clamps, is pulled upward by an Instron.
  • the Instron simultaneously measures the force exerted and the distance pulled. Integration of the area under the force vs. displacement curve divided by the area of the mesh strip gives the interfacial energy per unit area, which is the figure of merit determined by the test.
  • the table below shows the Energy/ Area (E/ A) results in units of J/m 2 for all the tests performed. For each set of samples, the average E/A value and the standard deviation were calculated.
  • sample 6 1% aminopropyltriethoxysilane
  • sample 9 1% aminopropyltrimethoxysilane
  • Visual Inspection Test areas can be coated with the materials of the invention and compared against untreated test areas using visual inspection.
  • Atomic Force Microscopy is a technique in which a very fine stylus tip is passed over a sample surface to measure its topography. This technique can make topographic images of surface roughness and can provide average measurements of surface roughness.
  • Z-range is the verticle distance from the highest to lowest point on the surface in the region scanned.
  • RMS is the root-mean-square average roughness over the whole image.
  • AFM testing shows the materials of the invention to have a Z-range of from about 0.5 microns to about 70 microns, and more preferably about 1.2 microns and an rms roughness range of from about 40 nm to about 1 micron and more preferably about 80 nm.
  • the blend reactions are carried out in a fume hood using a 3 neck round bottom flask equipped with a condenser and a mechanical stirrer and is purged continuously with nitrogen.
  • 32 mL hydroxy terminated polydimethylsiloxane having a viscosity of 8,000 cSt at 25 0 C and 0.386 g of benzoyl peroxide are added to the reactor and the mixture is stirred vigorously for 20 minutes.
  • 12.3 mL styrene and 35.4 mL n butyl acrylate are added to the reactor and the mixture is stirred continuously for 20 minutes.
  • 20 mL deionized water is added and the system is stirred for 20 minutes.
  • the reactor is then immersed in a water bath having a temperature of 100 0 C.
  • the color changes to pale white within 10 minutes, and the color and viscosity increases continuously throughout the reaction.
  • the condenser ias removed during the last 15 minutes in order to strip off most of the water.
  • the white viscous polymer is collected and further dried in a vacuum oven.
  • reaction is carried out as above but 32 inL of a hydroxy-terminated polysiloxane having a viscosity of 20,000 CSt at 25 0 C is used with 18.5 mL of styrene, 52.6 mL of n-butyl acrylate, 0.836 g benzoyl peroxide, and 20 mL of deionized water.
  • Examples 1 and 2 can be carried out in variou solvents including, but not limited to toluene, ether, tetrahydrofuran (THF), benzene, dichloromethane, and hexanes.
  • the viscosities of polysiloxanes can range from between about 10 to about 100 cSt at 25 0 C, about 2000 to about 8000 cSt at 25 0 C, and about 10,000 to about 50,000 cSt at 25 °C. In certain embodiments, the viscosity of the polysiloxane is 3500 cSt.
  • initiators include but are not limited to benzoyl peroxide, di-t-butylperoxide, cumene hydroperoxide, t-butyl hydroperoxide, AIBN, azo-bis-alkylnitrile and di-tert-butyl peroxide.
  • Tie Coat and Top Coat are shown, without limitation, in Table 2 below. In each coat, the materials are divided into two parts (A & B) prior to mixing. Table 2: Tie Coat & Top coat formulations (A and B formulations in Metric Units)
  • This example describes the application of a duplex fouling release system of the invention to a concrete surface.
  • the concrete is sealed with Americoat Amerlock two part epoxy concrete sealer.
  • the sealer is rolled on with a 1/4 inch nap roller.
  • the toughening tie layer resin is prepared as follows. 2 liters of the reactively stabilized organopolysiloxane blend prepared according to Example 1 and 1.5 liters of hexane are mixed until the viscosity of the organopolysiloxane is reduced considerably. After 10 minutes, 500 ml of Wacker CA40, a curing agent, is added and the material is mixed. The tie coat is applied to the surface with a 1 A inch nap roller. The release layer is applied over the tie layer about two hours after the tie layer application is complete. Four liters of Momomentive Performance Materials RTV-11 silicone release layer material is mixed with a tin based catalyst, and is applied immediately.
  • the application is allowed to cure for two days and the coating is in excellent physical condition at each inspection at year two and year three.
  • This example describes the application of a monoplex fouling release system of the invention to a concrete surface.
  • the concrete is sealed with Americoat Amerlock two part epoxy concrete sealer.
  • the sealer is rolled on with a 1/4 inch nap roller.
  • the mixed toughening tie layer / surface coat resin is prepared as follows. 4 liters of the reactively stabilized organopolysiloxane blend prepared according to Example 1 and 1.5 liters of hexane are mixed until the viscosity of the organopolysiloxane is reduced considerably. One liter of Momentive Performance Materials RTV-11 silicone release layer material is further added and is stirred for 10 minutes. After 10 minutes, 500 ml of Wacker CA40, a curing agent, is added and the material is mixed. CA40 can be used to cure both components of the monoplex. Alternatively DBT (a surface coat curing agent) also works to cure both components of the monoplex. In certain embodiments, the system is a somewhat better when cured with DBT.
  • the tie layer / surface coat resin is applied to the surface with a pressurized spray dispenser.
  • the application is allowed to cure for two days.
  • test patch or full coating system Prior to coating a surface, the following preparations should be made: test patch or full coating system; visit site, check condition of item to be painted, verify substrate is wood, steel, fiberglass or if surface prep is complete or if any repairs are required; review containment or ventilation requirements; review if pressure wash, abrasive blast, or soda blast is required; verify square footage and estimate quantity of paint needed; determine wehther special access requirements are needed; record equipment and materials needed; list test equipment required and check operation, will test panels be coated also; paint pumps epoxy, tie coat, surface coat; determine sufficient spray line, spray guns, tips and spare parts; check schedule to be sure sufficient dry and recoat times; check weather forecast; check if paint is on site, check quantities and batch numbers; discuss application schedule with applicator; and separate dedicated spray pumps and lines used for epoxy, tie and surface coats.
  • Clean spray equipment immediately. Check coating at recommended dry/re- coat times. Take and record dry film thickness measurements. (5-7 mils) Use plastic shim if coating is somewhat soft (be sure to subtract shim thickness from measurement. If coating is dry to touch proceed with next coat if ambient conditions are acceptable.
  • Coat 2 epoxy- tethering agent
  • mix proper amount of tethering agent with epoxy Completely mix components and allow 10-15 minutes sweat in time prior to application.
  • Duplex System Full Hull Application, Spray Application Vessel: Hinckley Picnic Boat - Length: 36 Feet, Beam: 12 Feet
  • the Duplex System is applied to a Hinckley 36 foot Picnic Boat. This is a pleasure yacht powered by a Water Jet engine.
  • the hull is composed of carbon fiber/kevlar/epoxy/e-glass composite.
  • the Duplex System is applied using standard spray application techniques well know by those practiced in the art of marine paint application.
  • the application is as follows:
  • the vessel is hauled and positioned in an outdoor protected shipyard space and is supported on the keel and is held upright by three jack stands each port and starboard. All layers of the Duplex System are applied with airless spray equipment using a cross-hatched application spray technique as described herein.
  • the copper ablative bottom paint is removed using a grit blast of baking soda.
  • the bottom up to the waterline is clean down to the composite surface.
  • the first layer of epoxy is applied on day 1 of Duplex System installation.
  • the weather is clear and dry, temperature is in the high 70 0 F low 80 0 F range and humidity is approximately 50%.
  • the first layer of epoxy is comprised of Sea Guard 5000 from Sherwin Williams. This layer is applied with a 36:1 airless sprayer (Graco) operating at 60 psi.
  • the first coat of epoxy is applied (8 to 9 mil wet film thickness) in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 4 hours to reach the reapplication state.
  • the second layer of epoxy is comprised of Sea Guard 5000 from Sherwin Williams and contains about 15% by volume of SCM501C from Momentive Performance Materials, Inc. This layer is applied with the same 36:1 airless sprayer (Graco) operating at the same pressure. This layer of epoxy is applied in approximately 15 minutes (8 to 9 mil wet film thickness) and is left overnight before the application of the Duplex System Tie Coat the following morning. Note: This second layer of epoxy may be allowed to reach a dry tack state, approximately 4 hours before the application of the Tie Coat. In this application, the Tie Coat is applied the following day for applicators convenience.
  • the Tie Coat is applied on day 2 of the Duplex System installation.
  • the weather is clear and dry, temperature was in the high 70 0 F low 80 0 F range and humidity is approximately 50%.
  • This layer is applied with a 54:1 airless sprayer (Graco) operating at approximately 60 psi.
  • the Tie Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 1.5 hours to reach the reapplication state.
  • the Surface Coat is applied on day 2 of the Duplex System installation once the Tie Coat achieves the dry tack state. This layer is applied with a 54: 1 airless sprayer (Graco) operating at approximately 75 psi. The Surface Coat is applied in approximately 15 minutes.
  • the repair system was applied as follows: a. Sea Guard 5000 marine epoxy is hand applied to the clean sections of the hull using a brush application. This first coat of epoxy is applied to a wet film thickness of approximately 9 mils and is allowed to proceed to a dryness of a dry tack. Drying time is approximately 3 hours. b. Sea Guard 5000 containing 15% SCM501C is hand applied to the first coat of epoxy (described in section (a) above). This second coat of epoxy is applied to a wet film thickness of approximately 9 mils and is allowed to proceed to a dryness of a dry tack.
  • Drying time is approximately 3 hours.
  • the Duplex System Tie Coat is hand applied to the second coat of epoxy using a brush application. This Tie Coat is applied to a wet film thickness of approximately 16 mils and is allowed to proceed to a dryness of a dry tack. Drying time is approximately 1.5 hours.
  • the Duplex System Surface Coat is hand applied to the surface of the Tie Coat using a brush application. This Surface Coat is applied to a wet film thickness of approximately 18 mils and is allowed to proceed to dryness.
  • the Hinckley Picnic Boat with the Duplex System installed is launched two days following the application of the Repair Kit.
  • the Duplex System is applied to the port bow section, at the water line, of a 700 ft barge that travels at approximately 8 knots. This is a vessel that plies the trade route between Jacksonville, Florida, USA to San Juan, Puerto Rico. The hull is steel. This application is chosen to evaluate the performance of the Duplex System on vessels traveling below 12 knots.
  • the Duplex System is applied using standard hand application techniques well know by those practiced in the art of marine paint application.
  • the application is as follows:
  • the vessel is placed in dry dock prior to extensive repairs including a an application of a standard copper ablative coating on the entire hull, with the exception of the DFRS Trial Patch, from the water line to the keel. All layers of the Duplex System are applied with roller painting technique.
  • the hull is prepared with grit blast to a standard white finish.
  • the entire Duplex System system is applied in a single day.
  • the first layer of epoxy is applied at approximately 1 PM.
  • the weather is clear and dry, temperature is in the mid 90° F range and humidity is approximately 85 to 90%.
  • the first layer of epoxy is comprised of Ameron 235 (Ameron Corporation). This first coat of epoxy is applied (8 to 9 mil wet film thickness) in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 2 hours to reach the reapplication state.
  • the second layer of epoxy is comprised of Ameron 235 (Ameron
  • This layer of epoxy is applied in approximately 15 minutes (8 to 9 mil wet film thickness) and is allowed to dry to a dry tack, taking approximately 2 hours to reach the reapplication state.
  • the Mist Coat is applied once the second epoxy coat achieves a dry tack state.
  • the Mist Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 30 minutes to reach the reapplication state.
  • the Tie Coat is applied once the Mist Coat achieves the dry tack state.
  • the Tie Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 1 hour to reach the reapplication state.
  • the Surface coat is applied once the Tie Coat achieves the dry tack state.
  • the Surface Coat is applied in approximately 15 minutes.
  • the vessel is launched once additional repairs to the hull are completed (more than one week following installation of the Duplex System Trial Patch).
  • the San Juan Jax Bridge with the Duplex System Trial Patch that is installed is inspected several times in the year following the application. Initially following the launch, the vessel spends approximately one month pier side while undergoing additional repairs in Veracruz, Mexico. During this time, the vessel encounteres a violent storm while pier side and sufferes severe abrasion of the starboard side including the area of the Duplex System Trial Patch. Upon inspection one month later in Jacksonville, FL, it is seen that the Duplex System Trial Patch suffered only minor scratching damage while the copper ablative coating on either side of the Duplex System Trial Patch is removed down to the steel hull. This demonstrates the extreme resilience of the Duplex System to impact damage.
  • the Duplex System is applied to an ocean cargo carrier.
  • the hull is composed steel.
  • the vessel is positioned in an outdoor dry dock.
  • the copper ablative bottom paint is removed using a grit blast.
  • the bottom up to the waterline is clean down to the steel surface.
  • the first layer of epoxy is applied on day 1 of Duplex System installation. The weather is overcast and dry, temperature is in the 80 0 F to 90 0 F range and humidity is approximately 70% to 80%.
  • the first layer of epoxy is comprised of Ameron 235 (Ameron Corporation, now PPG, Inc). The first coat of epoxy is applied (8 to 9 mil wet film thickness) in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 4 hours to reach the reapplication state.
  • the second layer of epoxy (applied on day 1 once the first epoxy reached the dry tack state) is comprised of Ameron 235 (Ameron Corporation) and contained 15% by volume of SCM501C from Momentive Performance Materials, Inc. This layer of epoxy is applied in approximately 15 minutes (8 to 9 mil wet film thickness) and is left overnight before the application of the DFRS Tie Coat the following morning. Note: This second layer of epoxy may be allowed to reach a dry tack state, approximately 4 hours before the application of the Tie Coat. In this application, the Tie Coat is applied the following day for applicators convenience.
  • the Tie Coat is applied on the day 2 of the Duplex System installation.
  • the weather is clear and dry, temperature is in the 80 0 F low 90 0 F range and humidity is approximately 80%.
  • the Tie Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 1.5 hours to reach the reapplication state.
  • the Surface coat is applied on day 2 of the Duplex System installation once the Tie Coat reaches the dry tack state.
  • the Surface Coat is applied in approximately 15 minutes. This vessel is launched several days after the application.
  • the Duplex System is applied to a section of tunnel 6 at the Electrabel Power Generating Station in Eemshaven, Netherlands.
  • the Duplex System is applied using standard hand application techniques well know by those practiced in the art of marine paint application.
  • the application is as follows:
  • the tunnel is dewatered and existing fouling organisms are removed by high pressure water wash. All layers of the Duplex System are applied with roller painting technique.
  • the tunnel walls are subjected to a wire brush treatment to remove any loose debris.
  • a first layer, epoxy concrete sealer, NuKlad 105 (Ameron Corporation) is applied.
  • the environmental conditions in the tunnel at the time of application has a temperature of approximately 60 0 F and humidity of approximately 50%.
  • the tunnel walls are dry but there is some residual water on the floor of the tunnel.
  • This first coat of epoxy is applied (8 to 9 mil wet film thickness) in approximately 15 minutes and is allowed to dry overnight.
  • a layer of epoxy is applied comprised of Ameron 235 (Ameron Corporation). This layer of epoxy is applied in approximately 15 minutes (8 to 9 mil wet film thickness) and is allowed to dry to a dry tack, taking approximately 3 hours to reach the reapplication state.
  • the Mist Coat is applied once the second epoxy coat reaches the dry tack state.
  • the Mist Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 30 minutes to reach the reapplication state.
  • the Tie Coat is applied once the Mist Coat reaches the dry tack state.
  • the Tie Coat is applied in approximately 15 minutes and is allowed to dry to a dry tack, taking approximately 1 hour to reach the reapplication state.
  • the Surface coat is applied once the Tie Coat had reached the dry tack state.
  • the Surface Coat was applied in approximately 15 minutes.
  • the Tunnel is placed back in service approximately one week following the installation of the Duplex System.
  • the Duplex System Trial Patch is inspected twice in the three years following installation. The Duplex System remains intact during this three year period demonstrating no detectable wear and extremely robust protection. Additionally, routine treatment with hot water does not diminished the longevity of the coating.
  • Loss coefficient (tan ⁇ ) was analyzed with full-automatic analyzer, VR-7120, Ueshima Seisakusho Co., Ltd.
  • the strip sample size is 2 mm (Thickness) x 5 mm (Width) x 40 mm (Length).
  • Measurement temperature was varied from minus 50-Celsius degree to plus 200-Celsius degree. Frequency was set at 1, 5,10,15,30,50,75,100Hz.
  • Loss coefficient (tan ⁇ ) was calculated by the following scheme.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)

Abstract

L'invention porte sur des compositions de mélanges stables, composées de mélanges de polysiloxane(s) et de polymère(s) organique(s). Ces mélanges polymères sont blancs et opaques, indiquant la présence d'une séparation de phase à l'échelle du micron. De tels mélanges peuvent être stockés à long terme (années) sans présenter de séparation de phases macroscopique. Ces mélanges stables sont obtenus sans réticulation substantielle, comme le prouve la dissolution facile du mélange polymère dans un solvant organique pour une caractérisation de masse moléculaire. Les mélanges stables de la présente invention sont particulièrement utiles comme matériaux de rembourrage, comme amortisseurs de vibration et suppresseurs de bruit.
PCT/US2009/000636 2008-02-08 2009-01-30 Mélanges polymères in situ à base de polysiloxane – matériaux d'amortissement pouvant être revêtus WO2009099574A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6511208P 2008-02-08 2008-02-08
US61/065,112 2008-02-08

Publications (1)

Publication Number Publication Date
WO2009099574A1 true WO2009099574A1 (fr) 2009-08-13

Family

ID=40952388

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/000636 WO2009099574A1 (fr) 2008-02-08 2009-01-30 Mélanges polymères in situ à base de polysiloxane – matériaux d'amortissement pouvant être revêtus

Country Status (1)

Country Link
WO (1) WO2009099574A1 (fr)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6265475B1 (en) * 1998-07-30 2001-07-24 Tokai Rubber Industries, Ltd. High damping material composition
WO2008013825A2 (fr) * 2006-07-25 2008-01-31 Fujifilm Hunt Smart Surfaces, Llc Compositions de mélanges polymères in-situ à base de polysiloxane articles et procédés d'élaboration correspondants

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6265475B1 (en) * 1998-07-30 2001-07-24 Tokai Rubber Industries, Ltd. High damping material composition
WO2008013825A2 (fr) * 2006-07-25 2008-01-31 Fujifilm Hunt Smart Surfaces, Llc Compositions de mélanges polymères in-situ à base de polysiloxane articles et procédés d'élaboration correspondants

Similar Documents

Publication Publication Date Title
US20080138634A1 (en) Polysiloxane based in situ polymer blends-compositions, articles and methods of preparation thereof
AU2008244254B2 (en) Anti-fouling coating compositions containing a carboxyl-functional organosilicone
TWI500718B (zh) 防污之塗料組合物及物理性防止積垢之方法
KR101656912B1 (ko) 수성 도료 조성물 및 도막 형성 방법
JP4647624B2 (ja) エポキシ防食塗料組成物、防食塗膜、およびオルガノポリシロキサン系防汚性複合塗膜、並びに該複合塗膜で被覆された船舶または水中構造物
JP4380960B2 (ja) 環境温度で硬化するコーティング組成物
US20090042042A1 (en) Tei Coat for Organopolysiloxane Antifouling Coat, Composite Coats, and Ships and Underwater Structures Covered with the Composite Coats
JP2007247290A (ja) コンクリート剥落防止表面被覆工法
JP2010504408A (ja) 低温で湿気硬化性の被覆用組成物および関連する方法
JP2006299132A (ja) 防汚塗料組成物
EP1526150A1 (fr) Composition de revêtement antidérapante
JP6866488B2 (ja) 汚損剥離コーティング組成物、該コーティング組成物でコーティングされた基材、および該コーティング組成物の使用
EP1646695B1 (fr) Composition de revetement protecteur de caoutchouc de silicone exempte de solvants
JP4093794B2 (ja) 船舶用プライマー防汚塗料組成物、船舶用複合防汚塗膜、該複合防汚塗膜の形成方法、該複合防汚塗膜で被覆された船舶および船舶外板の防汚方法
WO2021154501A1 (fr) Compositions de revêtement hydrophobe à base de liants organiques
US20110308424A1 (en) Single-Coat Self-Priming Anticorrosion Composition
JP4060701B2 (ja) プライマー防汚塗膜または複合防汚塗膜で被覆された水中構築構造物塗装体、および水中構築構造物の防汚方法
WO2009099574A1 (fr) Mélanges polymères in situ à base de polysiloxane – matériaux d'amortissement pouvant être revêtus
US11920052B2 (en) Waterborne, UV curable coating composition for easy-clean coatings
JP2004250517A (ja) コーティング組成物および被コーティング材
JP4430144B2 (ja) 塗料組成物
CN117203289A (zh) 防污涂料组合物
JP4750433B2 (ja) 共重合体およびその用途
JP2001240805A (ja) 塗料組成物
TW202122437A (zh) 用於容易清潔的塗層之水基性uv可固化塗料組合物

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09708299

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 09708299

Country of ref document: EP

Kind code of ref document: A1