WO2009099574A1

WO2009099574A1 - Polysiloxane based in situ polymer blends - coatable cushioning materials

Info

Publication number: WO2009099574A1
Application number: PCT/US2009/000636
Authority: WO
Inventors: Joseph P. Morris; Atsuo Kondo
Original assignee: Fujifilm Hunt Smart Surfaces, Llc
Priority date: 2008-02-08
Filing date: 2009-01-30
Publication date: 2009-08-13

Abstract

Stable blend compositions composed of mixtures of polysiloxane(s) and organic polymer(s) are claimed. These polymer blends are white and opaque indicating the presence of phase separation on the micron scale. Such blends can be stored for long periods of time (years) without exhibiting evidence of macroscopic phase separation. These stable blends are achieved without substantial crosslinking as evidenced by the fact that the polymer blend is readily dissolved in a suitable organic solvent for molecular weight characterization. The stable blends of the present invention have particular utility as cushioning materials, vibration dampeners, and noise suppressors.

Description

POLYSILOXANE BASED IN SITU POLYMER BLENDS - COATABLE

CUSHIONING MATERIALS

Related Applications

This application claims the benefit of U.S. provisional patent application Ser. No. 61/065,112, filed 08 February 2008 (Attorney Docket No. 81208P(301342)). The disclosure of the aforementioned patent application is incorporated herein in its entirety by this reference.

Incorporation Bv Reference

Each of the applications and patents cited in this text, as well as each document or reference cited in each of the applications and patents (including during the prosecution of each issued patent; "application cited documents"), and each of the PCT and foreign applications or patents corresponding to and/or paragraphing priority from any of these applications and patents, and each of the documents cited or referenced in each of the application cited documents, are hereby expressly incorporated herein by reference. More generally, documents or references are cited in this text, either in a Reference List, or in the text itself; and, each of these documents or references ("herein-cited references"), as well as each document or reference cited in each of the herein-cited references (including any manufacturer's specifications, instructions, etc.), is hereby expressly incorporated herein by reference.

Background

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. However, existing cushioning materials such as rubber, resin and plastics etc. is mainly processed at factories to apply to objects. For home use, 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

Summary of the Invention In one aspect, 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.

In another embodiment, 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.

In still another embodiment, the polysiloxane polymer of the tie coat polymer blend has the repeating unit formula

wherein Ri and R₂ 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.

In yet another embodiment, 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.

In another embodiment, 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.

In yet another embodiment, the organic polymer is styrene, butylacrylate, other alkylacrylates or a mixture thereof.

In still another embodiment, the in-situ generated free radicals are initiated by the addition of benzoyl peroxide or di-t-butylperoxide, cumene hydroperoxide, and t-butyl hydroperoxide. In another aspect of the invention, the tie coat polymer blend is comprised of further capable of being atomized and sprayed for application to a surface. In a further aspect, the tie coat polymer blend, further comprises a silicone fluid capable of increasing the sprayability of the blend.

In still yet another embodiment, the tie coat polymer is further capable of forming an intimate covalent bond matrix with a surface to which it is applied.

In another aspect of the invention, 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 25⁰C.

In another aspect of the invention, 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^CC.

In still another aspect of the invention, 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).

In another aspect, 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.

In one embodiment, the method further comprises contacting a free-radical initiator with the organopolysiloxane and/or organic monomer.

In some embodiments, 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.

In still another embodiment, the polysiloxane polymer has the repeating unit formula

In yet another embodiment, 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. In other embodiments, the hydroxyl terminated polydimethylsiloxane has viscosity of less than 100 centistokes at 25 ⁰C. In still other embodiments, the hydroxyl terminated polydimethylsiloxane has viscosity between 2000 to 8000 centistokes at 25 °C. In yet other embodiments, the hydroxyl terminated polydimethylsiloxane has viscosity between 10,000 to 50,000 centistokes at 25 ⁰C.

In yet another embodiment, the organic polymer is comprised of styrene, butyl acryl ate, other alkylacrylates or a mixture thereof.

In another embodiment, 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.

In still another embodiment, the method is performed in a nitrogen sparged atmosphere.

In another embodiment, the method further comprises contacting with a bifunctional tethering agent; preferrably the bifunctional tethering agent comprises a primary and/or secondary amine functionality and a siloxane-like functionality.

In yet another embodiment, 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.

In still another embodiment, 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. In yet another embodiment, the product produced by the method does not possess elongated microphase separated polymer morphology.

In still another embodiment, the method further comprising addition of water.

In another aspect, 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.

In one embodiment, 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.

In still another embodiment, the product is made by a process which further comprises the addition of water.

In one aspect, the invention provides a method of cushioning a surface comprising the step of contacting a surface with the cushioning material composition of the invention. In one embodiment, the cushioning is vibration suppression or noise suppression.

Detailed Description

Definitions

In order that the invention may be more readily understood, certain terms are first defined and collected here for convenience. Other definitions appear in context throughout the application.

In this disclosure, "comprises," "comprising," "containing" and "having" and the like can have the meaning ascribed to them in U.S. Patent law and can mean " includes," "including," and the like; "consisting essentially of or "consists essentially" likewise has the meaning ascribed in U.S. Patent law and the term is open-ended, allowing for the presence of more than that which is recited so long as basic or novel characteristics of that which is recited is not changed by the presence of more than that which is recited, but excludes prior art embodiments. As used herein, the term "cushioning" refers to the act of providing protection against or to absorb the shock of the force of an impact to a surface or substrate coated with the invention.

As used herein, the term "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.

As used herein, the term "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.

The term "crosslinking multifunctional monomers" refers to monomers which are capable of forming a crosslinked polymer chain when homopolymerized.

The term "halogen" refers to fluorine, chlorine, bromine or iodine.

As used herein, the term "alkyl" refers to a straight-chained or branched hydrocarbon group containing 1 to 50 carbon atoms. Examples of 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.

The term "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).

The term "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.

The term "alkoxy" refers to an -O-alkyl radical. The term "aryloxy" refers to an -O-aryl radical. An "amido" is an -C(O)NH₂.

As used herein the term "substituent" or "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. Examples of 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, mercapto, cyano, nitro, oxo (=0), thioxo (=S), or imino (=NR).

The term "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.

The term "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.

The term "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, indene monomers, maleic acid monomers, or fumaric acid monomers.

The term "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. In certain embodiments, the bifunctional tethering agent comprises a combination of primary and/or secondary amine functionality and a siloxane-like functionality. The term "siloxane-like functionality" refers to, typically, triethoxysilane and trimethoxysilane. The term "elongated morphology" refers to having morphological features in the phase separated or microphase separated material that are rod-like or needle-like.

The term "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.

The term "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.

The term "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.

The term "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).

The term "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.

It is also to be understood that the terminology used herein is for purposes of describing particular embodiments only, and is not intended to be limiting. As used in the specification and the appended claims, the singular forms "a", "an", and "the" include plural referents unless the context clearly indicates otherwise. Thus, for example, reference to "a peptide" includes multiple peptides, reference to "a spacer" includes two or more spacers.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the present application, including definitions will control. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference. Tie Coat Compositions

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.

In accordance with the present invention, the tie coat provides cushioning, vibration suppression and/or noise suppression properites via energy absorption. For example, 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. Or, 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. Also, 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.

Advantages of the 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. Example of Tie coat preparation:

1. A stainless mold form of 150 mm square is placed on a pan made of polypropylene or polyethylene.

2. Place 190 grams of the tie coat part A solution and 50 grams of tie coat part B solution into a wide mouthed poly plastic bottle.

3. Mix well with a spoon for 5 minutes till mixture becomes viscous. 4. Gently pour the mixed solution into the mold form.

5. Leave it for 5 to 7 days at well-ventilated place.

6. Slowly remove the mold form.

7. Cut the molded material out of the pan bottom.

2. 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.

3. It particularly excels for absorption of infrasonic frequency (below 20 Hz) that is widely believed to cause health problem by penetrating inside houses.

Anticorrosive Epoxy Coat containing a Tethering Agent to form Silicone-toSilicone Bonding In other aspects of the present invention, the anticorrosive epoxy layer further comprises a silane coupling agent having amines, such as primary and/or secondary amines. For example, 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.

Application to Surfaces

In certain embodiments, 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%.

In one embodiment, 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.

In another embodiment 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. Additionally, 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. Examples of bifunctional tethering agents contemplated by the present invention include SCM 501 C, aminopropyltriethoxysilane, aminopropyltrimethoxysilane, methylaminopropyltrimethoxysilane and cyclohexylaminopropyltrimethoxysilane. See Table 1 below.

Further contemplated by the invention is a 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.

Polvsiloxanes

The polysiloxanes used in this process are polymers that conform to the general repeating unit formula

where Riand R₂ 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 R₂ 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. These 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. 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 ⁰C.

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. In certain embodiments, 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.

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. 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 ⁰C. This liquid should have a low chain transfer constant, limiting its participation in the chemical reactions that are occurring. Preferentially, water may be used for this purpose even though it does not dissolve polysiloxanes or most vinyl monomers.

Generally it has been considered that crosslinking is required to generate stable polymer blends of the "interpenetrating polymer network" type. By 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. In our case, we are able to generate 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. During the reaction 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. However, 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. However, in the present case, 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. In one embodiment, the tie coat imparts mechanical strength and toughness to a top coat due to its chemical structure, physical properties and morphology. One example of a 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). 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. Additionally, 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 -150⁰C to about -60 ⁰C, preferably around -120⁰C, resulting in a soft surface coat. However, 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 0⁰C, preferably around -20⁰C. 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. Monolayer Systems

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.

In one aspect 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. In other aspects, the anticorrosive epoxy layer further comprises a silane coupling agent having amines, such as primary and secondaty amines. For example, a material known as 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.

In the monoplex single layer embodiment 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%. Conversly, 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%. In certain embodiments, 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. They may be present in the monoplex in amounts ranging from 0.1% to 40% based on the amount of mixed tie and surface coat mateials. In certain embodiments, a silicone fluid is added to aid the sprayability of the monoplex coating. In a further embodiment, the silicone fluid is selected from SF69 and SFl 147.

In other aspects, the tie coat polymer blend is modified to incorporate a perfluorinated acrylate or methacrylate (or some other fluorinated monomer). The incorporation of fluoropolymer into the tie coat improves its fouling release properties and may allow it to be used as the surface coat.

Duplex Systems

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.

Due to their bi-functional nature, 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.

Further, 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.). As such, Duplex System can, in some aspects, be applied directly to a substrate without the presence of an anticorrosive epoxy layer. In the aforementioned case of binding tie coat directly to fiberglass or vinyl ester, 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).

Articles and Coatings

Surface coat silicone viscosity contributes to the improved spray characteristics when the viscosity is reduced 10,000 to 12,000 centipose. At this range, the 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). 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.

Tablel: Examples of Tethering Agents Used in Second Epoxy Layer

Methods of Synthesis

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.

In one embodiment of manufacture, 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 100⁰C. We wished to maintain the temperature of the reactor at near 100⁰C 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 100⁰C to drive off the remaining water.

In another embodiment, a radial initiator, such as benzoyl peroxide, was utilized for grafting reactions. There are two methods for the addition of 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.

In other embodiments, it was determined that elongated morphologies and shear rates did not adversley affect the tie coats of the invention.

Bonding of Tie Coats to Surfaces

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. In one embodiment, 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.

In another embodiment, 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. In one embodiment, the surface coat surface tension is very low; about 20-25 dyne/cm. In another embodiment, the coat thickness ranges from about 8 to about 16 mil, preferably from about 10 to about 14 mil.

In certain embodiments, a silicone fluid is added to aid the sprayability of the tie coat. In a further embodiment, the silicone fluid is selected from SF69 and SFl 147.

In another embodiment the viscosity of the resin determines the extent of how well the paint will spray. We have discovered that 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.

Self-Assemblv - Silicone-to-Silicone Bonding While the inventors do not wish to be limited to any particular theory of chemical reaction or mechanism, it is believed that 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. When 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. These 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. This is again driven by the low surface energy of silicone surfaces and is facilitated by the lack of crosslinking in the tie coat polymer blend.Generally speaking, it is believed that the 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. As a result of this self-assembling feature, it is believed that 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.

It should be appreciated that the coatings or composites of the present invention, especially the Epoxy Coats containing Tethering Agents, Tie Coats and Surface Coats, 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.

In addition, it is contemplated by the present invention that the coatings or composites of the present invention, e.g., the free volume in the Surface Coats, 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. 5,259,701 entitled Antifouling Coating Composition Comprising Furan Compounds, Method for Protecting Aquatic Structures, and Articles Protected against Fouling Organisms, U.S. Patent No. 5,252,630 entitled Antifouling Coating and Method for Using Same, U.S. Patent No. 5,248,221 entitled Antifouling Coating Composition Comprising Lactone Compounds, Method for Protecting Aquatic Structures, and Articles Protected Against Fouling Organisms, U.S. Patent No. 4,788,302 entitled Anti-fouling Compound and Method of Use, U.S. Patent Publication Application No. 20060110456 entitled Method for Biocidal and/or Biostatic Treatment and Compositions therefore, U.S. Patent Publication Application No. 20050159454 entitled Materials and Methods for Inhibiting Fouling of Surfaces Exposed to Aquatic Environments, U.S. Patent Publication Application No. 20040235901 entitled Materials and Methods for Inhibiting Fouling of Surfaces Exposed to Aquatic Environments, 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. In: Recent Advances in Marine Biotechnology, Vol. II. M. Fingerman, R. Nagabhushanam, and M. -F. Thompson (eds), pp. xx. New Delhi: Oxford and IBH Publishing, and Rittschof, D. 1999, Natural product antifoulants: One perspective on the challenges related to coatings development. Biofouling (Special Issue).

Application Times

The 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. Thus, 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

The 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. Alternatively, 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.

Coat Thicknesses

The 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. In general 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. Furthermore, 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. Most preferably, 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. However, when the cushioning, vibration suppression and/or noise suppression properties of the tie coats are desired, 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).

Other Advantages

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

In order that the invention may be more fully understood, the following examples are provided. It should be understood that these examples are for illustrative purposes only and are not to be construed as limiting the invention in any way. Thus, the invention is further described by way of the following non-limiting examples.

Analytical Methods

The following methods may be used to characterize the structures of the various embodiments of this invention.

Size Exclusion Chromatography or Gel Permeation Chromatography

Molecular weights and polydispersities of the tie coat were determined by SEC/GPC in tetrahydrofuran at 30 ⁰C, using tetrahydrofuran as the mobile hase. Calibration wsw carried out using linear polystyrenes as standards.

Viscosity

Viscosity of the tie coat resin was measured using a Brookfield RTV viscometer and large spindles.

Physical Appearance

Polymers of the invention can be identified using 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

Elemental analysis was carried out by Galbraith Laboratories, Knoxville, TN.

Peel Test Analysis

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/m² for all the tests performed. For each set of samples, the average E/A value and the standard deviation were calculated.

Table: Tabulated Pull Test Results

Samples 1 and 2 with 30% and 15% SCM 501C respectively preformed very well and were statistically indistinguishable. Sample 3 with 5% SCM 501 C had a lower interfacial energy, i.e. performed less well by a statistically significant margin.

Of the alternative tethering additives sample 6 (1% aminopropyltriethoxysilane) and sample 9 (1% aminopropyltrimethoxysilane) produced the best results and to within the error of the experiments were the same as samples 1 and 2 (30% and 15% 501C). The alternative agents of samples 12 and 15 did not perform as well. The alternative tethering agent of Sample 18 produced the highest energy/area result but only three samples were successfully tested and the error for this set of data is very high. Thus it is difficult to draw conclusions for sample 18.

Visual Inspection Test areas can be coated with the materials of the invention and compared against untreated test areas using visual inspection.

Surface Roughness Analysis

Atomic Force Microscopy (AFM) 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. Two numbers are quoted, Z-range and RMS. 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 following examples are given by way of illustration only and are not to be considered limitations of this invention or many apparent variations of which are possible without departing from the spirit or scope thereof.

Example 1

Synthesis of a Polvsiloxane-Based In-Situ Polymer Blend

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. For example, 32 mL hydroxy terminated polydimethylsiloxane having a viscosity of 8,000 cSt at 25 ⁰C 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 ⁰C. The color changes to pale white within 10 minutes, and the color and viscosity increases continuously throughout the reaction. After 2-3 hours, the reaction is completed. 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.

Example 2 Synthesis of a Polysiloxane-Based In-Situ Polymer Blend

The reaction is carried out as above but 32 inL of a hydroxy-terminated polysiloxane having a viscosity of 20,000 CSt at 25 ⁰C 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 ⁰C, about 2000 to about 8000 cSt at 25 ⁰C, and about 10,000 to about 50,000 cSt at 25 °C. In certain embodiments, the viscosity of the polysiloxane is 3500 cSt. Additionally, 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.

Example 3

Exemplary Tie Coat & Top Coat Formulation

An exemplary formulation of Tie Coat and Top Coat as described herein 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)

Example 4

Application of a Duplex Tie Coat

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. Conditions for the sealer application: T = 60 ⁰C, 60% relative humidity. Eighteen hours after sealing the concrete surface, a coating of white, two part epoxy Amerlock 400 marine paint is applied to the surface with a ¹A inch nap roller. The anticorrosive epoxy marine paint is allowed to cure for 24 hours.

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 ¹A 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.

Example 5

Application of a Monoplex Tie Coat

This example describes the application of a monoplex fouling release system of the invention to a concrete surface.

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.

Example 6

Method of Coating a Surface with the Tie Coat of the Invention

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.

On Day 1 , check ambient conditions (temp, dew point, humidity, surface temp and forecast. Record data on application form. Check adjacent areas for potential overspray problems. Tape off surface areas not to be coated. Set-up equipment. Run airlines and layout paint lines. Stage paint and thinners for coat to be applied. Determine if repairs are complete (concrete may require sealer). Determine if surface is clean and ready to accept coating (solvent wipe, blow down). Be sure to have adequate solvents to clean pump, spray lines and gun. Mix epoxy coating 1 materials as recommended by manufacturer, check viscosity as needed. Stripe coat as needed (sharp edges, corners, tight areas). Apply coating, check wft (wet film thickness), apply even pattern and cross. Brush or roll out runs, sags. Touch-up holidays.

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. For 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. Check surface to be coated for cleanliness(visual). Clean as needed. Apply coating as on previous coat. Dry re- coat times may increase due to addition of tethering agent. Check wet film measurements. Brush out runs, sags as work progresses, touch-up holidays. Clean equipment. First and second coat of epoxy can generally be applied in the same day. If Tie coat can not be applied the next day, apply an additional epoxy coat with tethering agent.

On Day 2, check and record ambient conditions, check coating cure, check surface cleanliness(visual). Set-up equipment. Stage coating materials. For the Tie Coat, mix tie coat components, check viscosity of coating with viscosity cup and stopwatch (generally 20-25 seconds with #5 Zahn cup). Thinning not needed for this coat. Stripe coat sharp edges, corners and tight areas with spray as you go along. Check wet film thickness to gage how many passes are needed (10-14 dft). Check for and touch-up holidays as needed. Lightly brush out runs, sags as they occur. Clean-up spray pump, lines and spray gun immediately. Do not allow coating to set up in spray lines. Coating will cure faster at higher temperatures.

Allow 1 -2 hours dry time prior to Surface coat application. Coating should be dry to touch prior to Surface coat application. Check and record ambient conditions. Check surface cleanliness (visual). Check and record tie coat dry film thickness measurements, (use plastic shim method). Set-up equipment. Stage coating materials. For Surface coat, pre-mix part A surface coat. Add thinner as needed to achieve 40-45 seconds #5 Zahn cup. Approximately 15%. Add part B (hardener) after proper viscosity is achieved. Stripe coat sharp edges, corners and tight areas with spray as you go along. Lightly brush out sags, runs as they occur. High ambient temperatures will speed up cure times. Check wet film thickness to gage how many passes are needed (12-14dft). Clean spray pump, lines, spray gun immediately. Do not allow coating to set up in spray lines. Collect all paint waste for proper disposal.

Allow coating to cure 1 day minimum prior to removing masking materials. Lightly cut along tape line prior to removal. Do not cut into substrate. Allow adequate dry time (2 days) before moving jack stands. Touch-up jack stand locations using full four coat system. Solvent wipe substrate if needed. Surface coat by spray is preferred. It is preferred to step coatings around stands as they are applied. Epoxy, epoxy+ tethering agent, and tie coat should be applied up to existing coatings and not overlap. Surface coat should overlap existing surface coat slightly.

Example 7

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 70⁰F low 80⁰F 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 70⁰F low 80⁰F 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.

Two days following the application of the Surface Coat, the jack stands are moved so that untreated areas covered by the original placement of the jack stands are coated using the Duplex System Repair System. 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. c. 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. d. 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.

Example 8

Application: Duplex System with Mist Coat, Trial Patch, Hand Application Vessel: San Juan Jax Bridge Trial: 150 Square Foot Patch (approximately)

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

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 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.

Example 9

Application: Duplex System, Trial Patch (200 sq ft approximate), Roller Application by hand

Vessel: El Moro - Length: 700 Feet. Beam: 60 feet

The Duplex System is applied to an ocean cargo carrier. The hull is composed steel.

All layers of the Duplex System are applied using standard hand roller application techniques well know by those practiced in the art of marine paint application. The application is as follows:

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 80⁰F to 90⁰F 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 80⁰F low 90⁰F 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.

It is recommended that the Duplex System once applied is given 3 days to cure prior to launching the vessel.

Example 10

Power Utility Cooling Water Intake Tunnel: Eemshaven, Netherlands Application: Duplex System with Mist Coat, Trial Patch, Hand Application

The Duplex System is applied to a section of tunnel 6 at the Electrabel Power Generating Station in Eemshaven, Netherlands.

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 60⁰F 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.

On the second day of application of the Duplex System, 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.

Example 11

Loss coefficient (tan δ) 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 (tanδ) was calculated by the following scheme.

Storage Elastic Modulus E' = | σ/ε | cosδ Loss Elastic Modulus E"= | σ/ε | sinδ

Loss Coefficient tanδ = E' 7 E'

Loss Coefficient tanδ at 23±2°C

*Note: Commercialized product made of Polyurethane Equivalents

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents of the specific embodiments of the invention described herein. Such equivalents are intended with be encompassed by the following claims. Thus, while the present invention has been described in the context of embodiments and examples, it will be readily apparent to those skilled in the art that other modifications and variations can be made therein without departing from the spirit or scope of the present invention. Accordingly, it is not intended that the present invention be limited to the specifics of the foregoing description of the embodiments and examples, but rather as being limited only by the scope of the invention as defined in the claims appended hereto.

Claims

Having described our invention, we claim:

1. A tie coat polymer blend material having cushioning, vibration suppression and/or noise suppression properties, 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.

2. The tie coat polymer blend material of claim 1 wherein the polymer has a weight- average molecular weight of about 50,000 to 500,000.

3. The tie coat polymer blend material of claim 1 , wherein the polysiloxane polymer has the repeating unit formula

wherein Ri and R₂ are independently substituted or unsubstituted Ci-C₃ alkyl, or substituted or unsubstituted aryl, each of which may be substituted with cyano, halogen or another group which does not provide another linking functionality.

4. The tie coat polymer blend material of claim 3, wherein at least one terminal end of the polysiloxane polymer has at a terminal reactive group.

5. The tie coat polymer blend material of claim 4, wherein 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.

6. The tie coat polymer material of claim 5, wherein the polysiloxane polymer is hydroxyl terminated polydimethylsiloxane.

7. The tie coat polymer blend material of claim 1 further comprising an organic monomer or monomers capable of undergoing free radical polymerization in the presence of in-situ generated free radicals.

8. The tie coat polymer blend material of claim 7, wherein the organic polymer is comprised of mono-olefinic monomers.

9. The tie coat polymer blend material of claim 8, wherein the mono-olefinic monomers are 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.

10. The tie coat polymer blend material of claim 9, wherein the organic polymer is comprised of styrene, butylacrylate, other alkylacrylates or a mixture thereof.

11. The tie coat polymer blend material of claim 7, wherein the in-situ generated free radicals are initiated by the addition of benzoyl peroxide or di-t-butylperoxide, cumene hydroperoxide, and t-butyl hydroperoxide.

12. The tie coat polymer blend material of claim 1, further capable of being atomized and sprayed for application to a surface.

13. The tie coat polymer blend material of claim 12, further comprising a silicone fluid capable of increasing the sprayability of the blend.

14. The tie coat polymer blend material of claim 1 further capable of forming an intimate covalent bond matrix with a surface to which it is applied.

15. The tie coat polymer blend material of claim 1 having a viscosity of about 40,000 to about 400,000 centipoise at 25°C.

16. The tie coat polymer blend material of claim 15, having a viscosity of about 80,000 to about 250,000centipoise at 25°C.

17. The tie coat polymer blend material of claim 16, having a viscosity of about 95,000 to about 150,000 centipoise at 25°C.

18. The tie coat polymer blend material of claim 1, which further comprises a curing agent, wherein said curing agent is not a tin-based catalyst.

19. The tie coat polymer blend material of claim 18, wherein the curing agent is N,N',N" -Ttricyclohexyl-1 -methyl silanetriamine, tin-based, platinum-based, or titanium-based catalysts or other non-tin-based catalysts or an organic-based catalyst.

20. A method for preparing a material of claim 1 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.

21. The method of claim 20, further comprising contacting a free-radical initiator with the organopolysiloxane and/or organic polymer.

22. The method of claim 21, wherein the free-radical initiator is an azo-bis-alkylnitrile.

23. The method of claim 22, wherein the free-radical initiator is AIBN.

24. The method of claim 21, wherein the free-radical initiator is a peroxide.

25. The method of claim 24, wherein the free-radical initiator is benzoyl peroxide, di-t- butylperoxide, cumene hydroperoxide, and t-butyl hydroperoxide.

26. The method of claim 20, wherein the polysiloxane polymer has the repeating unit formula

wherein R| and R₂ 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.

27. The method of claim 20, wherein at least one terminal end of the polysiloxane polymer has a terminal reactive group.

28. The method of claim 27, wherein wherein 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.

29. The method of claim 27, wherein the polysiloxane polymer is hydroxyl terminated polydimethylsiloxane.

30. The method of claim 29, wherein the hydroxyl terminated polydimethylsiloxane is less than 100 centistoke at 25 ⁰C.

31. The method of claim 29, wherein the hydroxyl terminated polydimethylsiloxane is between 2000 to 8000 centistoke at 25 ⁰C.

31. The method of claim 29, wherein the hydroxyl terminated polydimethylsiloxane is between 10,000 to 50,000 centistoke at 25 ⁰C.

32. The method of claim 20, further comprising organic monomer(s) capable of undergoing free radical polymerization in the presence of in-situ generated free radicals.

33. The method of claim 20, wherein the organic polymer is comprised of mono-olefinic monomers.

34. The method of claim 33, wherein the mono-olefinic monomers are 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- vinylcarbazole 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.

35. The method of claim 20, wherein the organic polymer is styrene, butyl acryl ate, other alkylacrylates or a mixture thereof.

36. The method of claim 20, wherein the polymer has a weight-average molecular weight of about 50,000 to 500,000.

37. The method of claim 20 or 21 wherein the contacting is performed in a nitrogen sparged atmosphere.

38. The method of claim 20, further comprising contacting with a bifunctional tethering agent.

39. The method of claim 38, wherein the bifunctional tethering agent comprises an amine functionality and a siloxane-like functionality.

40. The method of claim 21 , wherein the initiator is introduced to the organopolysiloxane and/or organic polymer in a plurality of doses.

41. The method of claim 21 , wherein the initiator is introduced to the organopolysiloxane and/or organic polymer in a single dose.

42. The method of claim 20, further comprising contacting with a curing agent, wherein said curing agent is not a tin-based catalyst.

43. The method of claim 20, wherein the shear rate used during polymerization is from about 10 min^"1 to about 1500 min^"1.

44. The method of claim 20, wherein the product produced does not possess elongated phase separated or microphase separated polymer morphology.

45. The method of claim 20, further comprising addition of water.

46. A material product having cushioning, vibration suppression and/or noise suppression properties, said material product is 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 and where said organic polymer is prepared by exposure to in-situ generated free radicals in the presence of the polydimethylsiloxane.

47. The product of claim 46, further comprising contacting a free-radical initiator with the organopolysiloxane and organic monomers.

48. The product of claim 46, wherein the contacting is performed in a nitrogen sparged atmosphere.

49. The product of claim 461, wherein the process further comprises the addition of water.

50. A method of imparting cushioning, vibration suppression and/or noise suppression properties to a surface comprising the step of contacting a surface with the material composition of claim 1.

51. A method of imparting cushioning, vibration suppression and/or noise suppression properties to a surface comprising the step of positioning the material composition of claim 1 adjacent to a surface.