Field

This invention relates to an epoxy resin composition and its application in marine maintenance and repair coating with improved overcoatability.

Background

Epoxy resin is considered as the most cost-effective binder for anti-corrosion coating due to its excellent adhesion to metal, mechanical rigidity and chemical resistance properties. Epoxy primers are usually overcoated by a variety of topcoats, including solvent or water based epoxy, acrylate, polyurethane, polysiloxanes or other functional finishes.

There is an optimum time for epoxy to be overcoated, within this period no additional surface preparation is required. After the "overcoat window" has passed, the primer will need to be abraded before it can be topcoated, which is an expensive and labor-consuming process.

Overcoat window varies in each system according to the specific material and conditions applied. Temperature has significant influence on the overcoat window. 7 to 14 days are the typical overcoat window in most cases. Overcoating beyond the overcoat window will lead to weak intercoat adhesion and even paint failure, which causes significant scheduling issues or rework in the industry hampering throughput.

It is therefore, still interesting in the art to develop a coating having balanced overcoat window time and anti-corrosion properties.

Summary

The present invention provides a curable composition comprising, based on the total weight of the curable composition: a) from 1 wt.% to 20 wt.% an epoxy compound I selecting from aromatic epoxy compounds, alicyclic epoxy compounds, or a mixture thereof; b) from 1 wt.% to 20 wt.% a chlorinated polyolefin based terpolymer; and c) from 1 wt.% to 40 wt.% a curing agent. It may further comprises from 0.4 wt.% to 10 wt.% an epoxy compound II selecting from acyclic aliphatic epoxy compounds.

1

CORRECTED SHEET(RULE 91) Preferably, the epoxy compound I is bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, or a mixture thereof.

Preferably, the chlorinated polyolefin based terpolymer comprises from 5 to 20 mole percent structural units of vinyl chloride, from 4 to 10 mole percent structural units of vinyl acetate, and from 60 to 90 mole percent structural units of vinyl alcohol.

Optionally, the chlorinated polyolefin based terpolymer comprises from 5 to 20 mole percent structural units of vinyl chloride, from 70 to 90 mole percent structural units of vinyl acetate, and from 1 to 10 mole percent structural units of maleic acid.

Preferably, the epoxy compound II is glycerol diglycidyl ether, poly(propylene glycol) diglycidyl ether with an average molecular weight (Mw) from 300 to 1000, or the mixture thereof.

The present invention further provides a coating composition comprising, based on the total weight of the coating composition: a) from 25 wt.% to 45 wt.% a cured epoxy compound I selecting from aromatic epoxy compounds, alicyclic epoxy compounds, or a mixture thereof; b) from 1 wt.% to 20 wt.% a chlorinated polyolefin based terpolymer; and c) from 35 wt.% to 65 wt.% a filler. The coating composition may further comprises from 0.4 wt.%) to 25 wt.%) based on the total weight of the coating composition, a cured epoxy compound II selecting from acyclic aliphatic epoxy compounds. Detailed Description

As used herein, "a," "an," "the," "at least one," and "one or more" are used interchangeably. The term "and/or" means one, one or more, or all of the listed items. The recitations of numerical ranges by endpoints include all numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, 5, etc.).

For one or more embodiments, the curable compositions include an epoxy composition comprising an epoxy compound I and optionally, an epoxy compound II. A compound is a substance composed of atoms or ions of two or more elements in chemical combination and an epoxy compound is a compound in which an oxygen atom is directly attached to two adjacent or non-adjacent carbon atoms of a carbon chain or ring system. The epoxy compound I can be from 1 weight percent to 20 weight percent of the curable composition; for example the epoxy compound can be from 3 weight percent to 16 weight percent or from 5 weight percent to 15 weight percent of the curable composition. In some embodiments that comprises epoxy compound II, it can be from 0.4 weight percent to 10 weight percent of the curable composition; for example the epoxy compound II can be from 1 weight percent to 8 weight percent or from 4 weight percent to 8 weight percent of the curable composition.

The epoxy compound I can be selected from the group consisting of aromatic epoxy compounds, alicyclic epoxy compounds, and combinations thereof.

The epoxy compound II can be selected from the group consisting of acyclic aliphatic epoxy compounds.

Examples of aromatic epoxy compounds include, but are not limited to, glycidyl ether compounds of polyphenols, such as hydroquinone, resorcinol, bisphenol A, bisphenol F, 4, 4'- dihydroxybiphenyl, phenol novolac, cresol novolac, trisphenol (tris-(4- hydroxyphenyl)methane), 1, 1, 2, 2-tetra(4- hydroxyphenyl)ethane, tetrabromobisphenol A, 2, 2-bis(4-hydroxyphenyl)-l, 1, 1, 3, 3, 3- hexafluoropropane, 1 , 6-dihydroxynaphthalene, and combinations thereof.

Examples of alicyclic epoxy compounds include, but are not limited to, polyglycidyl ethers of polyols having at least one alicyclic ring, or compounds including cyclohexene oxide or cyclopentene oxide obtained by epoxidizing compounds including a cyclohexene ring or cyclopentene ring with an oxidizer. Some particular examples include, but are not limited to, hydrogenated bisphenol A diglycidyl ether; 3, 4-epoxycyclohexylmethyl-3, 4- epoxycyclohexyl carboxylate; 3, 4-epoxy-l-methylcyclohexyl-3, 4-epoxy-l-methylhexane carb xylate; 6-methyl-3, 4-epoxycyclohexylmethyl-6-methyl-3, 4-epoxycyclohexane carboxylate; 3, 4-epoxy-3-methylcyclohexylmethyl-3, 4-epoxy-3-methylcyclohexane carboxylate; 3, 4-epoxy-5-methylcyclohexylmethyl-3, 4-epoxy-5-methylcyclohexane carboxylate; bis(3, 4-epoxycyclohexylmethyl)adipate; methylene-bis(3, 4- epoxycyclohexane); 2, 2- bis(3, 4-epoxycyclohexyl)propane; dicyclopentadiene diepoxide; ethylene-bis(3, 4- epoxycyclohexane carboxylate); dioctyl epoxyhexahydrophthalate; di-2- ethylhexyl epoxyhexahydrophthalate; and combinations thereof.

The term "acyclic aliphatic epoxy compound" refers to a hydrocarbon compound having linear structure (straight or branched) onto which epoxides are attached. Besides hydrogen, other elements can be bound to the carbon chain; the most common examples are oxygen, nitrogen, sulphur, and chlorine. The acyclic aliphatic epoxy resin may be a monoepoxide compound or a compound containing two or more epoxy groups. Preferably, the acyclic aliphatic epoxy resin has two or more epoxy groups. The acyclic aliphatic epoxy resin may include acyclic aliphatic epoxides modified with glycols.

Acyclic aliphatic epoxy compounds include three identified types, epoxidized diene polymers, epoxidized oils and derivatives, and polyglycol diepoxides. Epoxidized diene polymers are epoxidation of polymers containing ethylenic unsaturation which can by prepared by copolymerizing one or more olefins, particularly diolefins, by themselves or with one or more alkenyl aromatic hydrocarbon monomers. The copolymers may, of course, be random, tapered, block or a combination of these, as well as linear, star of radial. Diene polymers can be epoxidized include, but are not limited to, polymers of butadiene alone, random copolymers of butadiene and styrene, random copolymers of butadiene and (meta)acrylonitrile, block copolymers of butadiene and styrene, random copolymers of isoprene and styrene, random copolymers of isoprene and (meta)acrylonitrile, block copolymers of isoprene and styrene, and copolymers of butadiene and isoprene. In some cases, the copolymers of butadiene and isoprene may include vinyl compounds such as styrene and (meta)acrylonitrile.

Epoxidized oils and derivatives are epoxidized fatty acid esters. The oils from which these products are derived are naturally occurring long chain fatty acid sources, and there is considerable overlap in the composition of the fatty acid portion of these products. They are primarily the C ₁₈ acids: oleic, linoleic, and linolenic acid. The alcohols are primary alcohols, diols or triols. This category consists of related fatty acid esters. Fatty acids, tall-oil, epoxidized, 2-ethylhexyl esters (ETP) 9-Octadecanoic acid (Z)-, epoxidized, ester w/propylene glycol (EODA) Epoxidized soybean oil (ESBO) Epoxidized linseed oil (ELSO or ELO). ETP is a monoester with 2-ethylhexanol. EODA is a diester with propylene glycol. ESBO and ELSO are triesters with glycerol (triglycerides).

Polyglycol diepoxides can be presented as formula I. The preferred compounds of formula I include those derived from ethylene and propylene glycols, in particular ethylene glycol and polyethylene glycol, with an average molecular weight of from 100 to 1500, preferably 200 to 800, in particular 600. In formula I, m preferably signifies 7 to 30, more preferably 7 to 14.

H— CH20(CHR'CH ₂ 0)mCH2—

R' signifies hydrogen or methyl, and m signifies an integer of from 1 to 40,

Examples of polyglycol diepoxides include, but are not limited to, 1, 4-butanediol diglycidyl ether, and 1, 6- hexanediol diglycidyl ether; glycerol diglycidyl ether; a triglycidyl ether of glycerin; a triglycidyl ether of trimethylol propane; a tetraglycidyl ether of sorbitol; a hexaglycidyl ether of dipentaerythritol; a diglycidyl ether of polyethylene glycol, such as ethylene glycol diglycidyl ether, and diethylene glycol diglycidyl ether; and a diglycidyl ether of polypropylene glycol, such as, propylene glycol diglycidyl ether; polyglycidyl ethers of polyether polyols obtained by adding one type, or two or more types, of alkylene oxide to aliphatic polyols such as propylene glycol, trimethylol propane, and glycerin, such as, tripropylene glycol diglycidyl ether, and propylene glycol diglycidyl ether; diglycidyl esters of aliphatic long-chain dibasic acids; and combinations thereof.

An extensive enumeration of epoxy compounds useful in the present invention is found in Lee, H. and Neville, K., "Handbook of Epoxy Resins," McGraw-Hill Book Company, New York, 1967, Chapter 2, pages 257-307.

Preferably, the epoxy compound I is aromatic epoxy compound obtained from the reaction of epichlorohydrin and a polyol, such as 4, 4'-isopropylidenediphenol (bisphenol- A). , more preferably, it is bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, or the mixture thereof. These epoxy resins are normally liquids or have a low molecular weight and are soluble in various aliphatic solvents such as ketones, esters, ether alcohols or any of the aromatic solvents such as xylene, ect.

Preferably, the epoxy compound I useful in the present invention for the preparation of the curable compositions, are selected from commercially available products. For example, D.E.R.™ 331, D.E.R.™ 332, D.E.R.™ 334, D.E.R.™ 337, D.E.R.™ 383, D.E.R.™ 580, D.E.R.™ 736, or D.E.R.™ 732 available from The Dow Chemical Company may be used. Most preferably, the epoxy compound I is a liquid epoxy resin, such as D.E.R.™ 331 having an average epoxide equivalent weight of 190 and D.E.R.™ 337 having an average epoxide equivalent weight of 240.

Preferably, the epoxy compound II is polyglycol diepoxides and polyglycol diepoxides modified with glycols , more preferably it is a diglycidyl ether of polypropylene glycol such as poly(propylene glycol) diglycidyl ether with an average molecular weight (Mw) from 300 to 1000 and glycerol diglycidyl ether.

For one or more embodiments, the curable compositions include a curing agent. The curing agent can be selected from the group consisting of novolacs, amines, anhydrides, carboxylic acids, phenols, thiols, and combinations thereof. The curing agent can be from 1 weight percent to 40 weight percent of the curable composition; for example the curing agent can be from 20 weight percent to 40 weight percent or from 25 weight percent to 35 weight percent of the curable composition.

For one or more of the embodiments, the curing agent can include a novolac. Examples of novolacs include phenol novolacs. Phenols can be reacted in excess, with formaldehyde in the presence of an acidic catalyst to produce phenol novolacs. For one or more of the embodiments, the curing agent can include an amine. The amine can be selected from the group consisting of aliphatic polyamines, arylaliphatic polyamines, cycloaliphatic polyamines, aromatic polyamines, heterocyclic polyamines, polyalkoxy polyamines, dicyandiamide and derivatives thereof, aminoamides, amidines, ketimines, and combinations thereof. The preferred amine curing agents are the C2-C10 polyamines that contain two or more reactive hydrogen groups and amine-terminated polyamide compositions, including those formed through the condensation of unsaturated fatty acids with C ₂ -Cio aliphatic polyamines having at least three amino groups per molecular. Sufficient amounts of the amine curing agent are employed to assure substantial crosslinking of the epoxide resin. Generally stoichiometric amounts or slight excess of the amine curing agent are employed. Amine curing agents are normally used in amounts varying from 20-75 wt. percent based upon the type of the epoxy resin.

Examples of aliphatic polyamines include, but are not limited to, ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), trimethyl hexane diamine (TMDA), hexamethylenediamine (HMD A), N-(2- aminoethyl)-l ,3-propanediamine (N3- Amine), N, N'-l , 2-ethanediyl- bis- 1 , 3- propanediamine ( 4-amine), dipropylenetriamine, and reaction products of an excess of these amines with an epoxy resin, such as bisphenol A diglycidyl ether.

Examples of arylaliphatic polyamines include, but are not limited to, m- xylylenediamine (mXDA), and p-xylylenediamine. Examples of cycloaliphatic polyamines include, but are not limited to, 1, 3-bisaminocyclohexylamine (1, 3-BAC), isophorone diamine (IPDA), 4, 4'-methylenebiscyclohexaneamine, and bis(secondary amine) like JEFFLINK 754 from Huntsman Chemical Company.

Examples of aromatic polyamines include, but are not limited to, m- phenylenediamine, diaminodiphenylmethane (DDM), and diaminodiphenylsulfone (DDS). Examples of heterocyclic polyamines include, but are not limited to, N-aminoethylpiperazine (NAEP), 3, 9-bis(3-aminopropyl) 2, 4, 8, 10-tetraoxaspiro(5, 5)undecane, and combinations thereof.

Examples of polyalkoxy polyamines include, but are not limited to, 4, 7-dioxadecane- 1 , 10-diamine; 1-propanamine; (2, l-ethanediyloxy)-bis-(diaminopropylated diethylene glycol) (ANC AMINE ^® 1922 A); poly(oxy(methyl-l, 2- ethanediyl)), alpha-(2- aminomethylethyl)omega-(2-aminomethylethoxy) (JEFF AMINE ^® SD-231, SD-401, SD- 2001); triethyleneglycoldiamine; and oligomers (JEFF AMINE ^® EDR-148, EDR-176); poly(oxy(methyl-l,2- ethanediyl)), alpha, alpha'-(oxydi-2, 1 -ethanediyl)bis(omega- (aminomethylethoxy)) (JEFF AMINE XTJ-511); bis(3-aminopropyl)polytetrahydrofuran 350; bis(3- aminopropyl)polytetrahydrofuran 750; poly(oxy(methyl-l, 2-ethanediyl)); a- hydro- (2-aminomethylethoxy) ether with 2-ethyl-2-(hydroxymethyl)- 1, 3 -propanediol (JEFF AMINE ^® T-403); diaminopropyl dipropylene glycol; and combinations thereof.

Examples of dicyandiamide derivatives include, but are not limited to, guanazole, phenyl guanazole, cyanoureas, and combinations thereof.

Examples of aminoamides include, but are not limited to, amides formed by reaction of the above aliphatic polyamines with a stoichiometric deficiency of anhydrides and carboxylic acids, as described in U.S. Patent 4,269,742.

Examples of amidines include, but are not limited to, carboxamidines, sulfinamidines, phosphinamidines, and combinations thereof.

Examples of ketimines include compounds having the structure (R ² ) ₂ C = NR ³ , where each R ² is an alkyl group and R ³ is an alkyl group or hydrogen, and combinations thereof.

For one or more of the embodiments, the curing agent can include phenalkamine. Phenalkamine is the condensation product of an alkyl phenol, aldehyde and one more at least difunctional amines and are known by the skilled man as Mannich bases: the reaction product of an aldehyde, such as formaldehyde, amine and an alkyl phenol (see WO 2004/024792 Al, page 3, lines 16-18). Useful amines include ethylenediamine (EDA), diethyltriamine (DETA) (see WO 2004/024792 Al, page 3, lines 18-19), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), m-xylylendiamine (MXDA), isophorone diamine, and the mixture thereof. Most preferably, a mixture of TETA and TEPA is used as amine mixture; the alkyl phenol is a cardanol-containing extract derived from cashew nutshell liquid (see WO 2004/024792 Al, page 3, lines 19-20).

For one or more of the embodiments, the curing agent can include an anhydride. An anhydride is a compound having two acyl groups bonded to the same oxygen atom. The anhydride can be symmetric or mixed. Symmetric anhydrides have identical acyl groups. Mixed anhydrides have different acyl groups. The anhydride is selected from the group consisting of aromatic anhydrides, alicyclic anhydrides, aliphatic anhydride, polymeric anhydrides, and combinations thereof.

Examples of aromatic anhydrides include, but are not limited to, 3, 3', 4, 4'- benzophenonetetracarboxylic dianhydride, pyromellitic anhydride, and combinations thereof.

Examples of alicyclic anhydrides include, but are not limited to methyltetrahydrophthalic anhydride, tetrahydrophthalic anhydride, methyl nadic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, and combinations thereof. Examples of aliphatic anhydrides include, but are not limited to, propionic anhydride, acetic anhydride, and combinations thereof.

Example of a polymeric anhydrides include, but are not limited to, polymeric anhydrides produced from copolymerization of maleic anhydride such as poly(styrene-co- maleic anhydride) copolymer, and combinations thereof.

For one or more of the embodiments, the curing agent can include a carboxylic acid. Examples of carboxylic acids include oxoacids having the structure R ⁴ C(=0)OH, where R ⁴ is an alkyl group or hydrogen, and combinations thereof.

For one or more of the embodiments, the curing agent can include a phenol. Examples of phenols include, but are not limited to, bisphenols, novolacs, and resoles that can be derived from phenol and/or a phenol derivative, and combinations thereof.

For one or more of the embodiments, the curing agent can include a thiol. Examples of thiols include compounds having the structure R ⁵ SH, where R ⁵ is an alkyl group, and combinations thereof.

The curable composition of the present invention further comprises from 1 wt.% to 20 wt.% based on the total weight of the curable composition, a chlorinated polyolefin based terpolymer. Preferably, it is from 3 wt.% to 13 wt.%.

In one embodiment, the chlorinated polyolefin based terpolymer is a terpolymer of vinyl chloride, vinyl acetate, and vinyl alcohol. It contains vinyl chloride repeat units in an amount of from about 5% to about 20% mole percent, vinyl alcohol repeat units in an amount of from about 60% to about 90% mole percent, and vinyl acetate repeat units in an amount of from about 4% to about 10% mole percent. Preferably, the terpolymer contains vinyl chloride repeat unites in an amount of from about 14% to about 15% mole percent, vinyl alcohol repeat units in an amount of from about 70% to about 80% mole percent, and vinyl acetate repeat units in an amount of from 1% to about 5% mole percent, although the relative amounts of monomers can be outside of these ranges.

The terpolymer of vinyl chloride, vinyl acetate, and vinyl alcohol typically has a weight average molecular weight (Mn) of from about 25000 to about 40000 and more preferably from about 30000 to about 35000, although the weight average molecular weight can be outside of these ranges.

Suitable poly(vinyl chloride-vinyl alcohol-vinyl acetate) terpolymers can be prepared by, for example, high pressure free radical polymerization of vinyl chloride with vinyl acetate in a suitable solvent, such as water, benzene, toluene, cyclohexane, or the like, to from a poly(vinyl chloride-vinyl acetate) copolymer, followed by hydrolysis of the poly (vinyl chloride-vinyl acetate) copolymer to obtain a poly(vinyl chloride-vinyl alcohol- vinyl acetate) terpolymer.

One commercial product of such suitable poly(vinyl chloride-vinyl alcohol-vinyl acetate) terpolymers is CONVINYL ^® G-75 with Mn equaling to about 32000, Vac content being 4%, and hydroxyl value being 75 from Connell Bros. Company LTD.

In another embodiment, chlorinated polyolefin based terpolymer is a terpolymer of vinyl chloride, vinyl acetate, and maleic acid. It contains vinyl chloride repeat units in an amount of from about 5% to about 20% mole percent, vinyl acetate repeat units in an amount of from about 70% to about 90% mole percent, and maleic acid repeat units in an amount of from about 1% to about 10%> mole percent. Preferably, the terpolymer contains vinyl chloride repeat units in an amount of from about 10%> to about 15% mole percent, vinyl acetate repeat units in an amount of from about 80% to about 90% mole percent, and maleic acid repeat units in an amount of from 1% to about 5% mole percent, although the relative amounts of monomers can be outside of these ranges.

The terpolymer typically has a weight average molecular weight (Mn) of from about

20000 to about 40000 and more preferably from about 28000 to about 32000, although the weight average molecular weight can be outside of these ranges.

Suitable poly(vinyl chloride-vinyl acetate-maleic acid) terpolymers can be prepared by, for example, high pressure free radical polymerization of vinyl chloride with vinyl acetate and maleic acid in a suitable solvent, such as water, benzene, toluene, cyclohexane, or the like, to from a poly( vinyl chloride- vinyl acetate-maleic acid) terpolymer.

One commercial product of such suitable poly(vinyl chloride-vinyl alcohol-vinyl acetate) terpolymers is CONVINYL ^® C-47 with Mn equaling to 29000 and Vac: Vcm: Mai being 13 :86: 1 from Connell Bros. Company LTD.

For one or more embodiments, the curable compositions can include a catalyst.

Examples of the catalyst include, but are not limited to, 2-methyl imidazole, 2-phenyl imidazole, 2-ethyl-4-methyl imidazole, 1 -benzyl-2-phenylimidazole, boric acid, triphenylphosphine, tetraphenylphosphonium-tetraphenylborate, and combinations thereof. The catalyst can be used in an amount of from 0.01 to 5 parts per hundred parts of the epoxy compound; for example the catalyst can be used in an amount of from 0.05 to 4.5 parts per hundred parts of the epoxy compound or 0.1 to 4 parts per hundred parts of the epoxy compound.

For one or more embodiments, the curable compositions can include an inhibitor. The inhibitor can be a Lewis acid. Examples of the inhibitor include, but are not limited to, boric acid, halides, oxides, hydroxides and alkoxides of zinc, tin, titanium, cobalt, manganese, iron, silicon, boron, aluminum, and combinations thereof. Boric acid as used herein refers to boric acid or derivatives thereof, including metaboric acid and boric anhydride. The curable compositions can contain from 0.3 mole of inhibitor per mole of catalyst to 3 mole of inhibitor per mole of catalyst; for example the curable compositions can contain from 0.4 moles of inhibitor per mole of catalyst to 2.8 mole of inhibitor per mole of catalyst or 0.5 mole of inhibitor per mole of catalyst to 2.6 mole of inhibitor per mole of catalyst.

The curable composition may also include one or more optional additives conventionally found in epoxy resin systems to form the coating composition of the present invention. For example, the curable composition of the present invention may contain additives such as nonreactive and reactive diluents; catalyst; other curing agents; other resins; fibers; coloring agents; thixotropic agents, photo initiators; latent photo initiators, latent catalysts; inhibitors; flow modifiers; accelerators; desiccating additives; surfactants; adhesion promoters; fluidity control agents; stabilizers; ion scavengers; UV stabilizers; flexibilizers; fire retardants; diluents that aid processing; toughening agents; wetting agents; mold release agents; coupling agents; tackifying agents; and any other substances which are required for the manufacturing, application or proper performance of the composition.

Fillers are used to control the viscosity, rheology, shelf stability, specific gravity and cured performance properties, such as corrosion resistance, impact resistance and abrasion resistance. The fillers may be spherical or platy. As used herein platy means the particles have a high aspect ratio. High aspect ratio fillers include as talc, mica and graphite. Preferred high aspect ratio fillers include mica having a median particle size of 20 to 70 microns (micrometers) and most preferably 50 microns (micrometers). Examples of fillers include such as wollastonite, barites, mica, feldspar, talc, silica, crystalline silica, fused silica, fumed silica, glass, metal powders, carbon nanotubes, grapheme, calcium carbonate, and barium sulphate; aggregates such as glass beads, polytetrafluoroethylene, polyol resins, polyester resin, phenolic resins, graphite, molybdenum disulfide and abrasive pigments; viscosity reducing agents; boron nitride; nucleating agents; dyes; pigments such as titanium dioxide, carbon black, iron oxides, chrome oxide, and organic pigments.

The coating composition of the present invention is made by batch mixing the necessary components under high speed, high shear agitation. The process includes three steps: all liquid resins, curatives and platy fillers are mixed first for 20 minutes and degassed at 30mHg; spherical fillers and glass spheres are added and the mixture is mixed for 20 minutes and degassed at 30mmHg; fumed silica is then added and the mixture is mixed for 10 minutes and degassed at 30 mmHg.

Other information related with the coating preparation is listed in patent: US20100048827(A1).

The coating composition of the present invention comprises based on the total weight of the coating composition a) from 25 wt.% to 45 wt.%, preferable from 30 wt.% to 45 wt.%, most preferably from 30 wt.% to 40 wt.%, a cured epoxy compound I; b) from 1 wt.% to 20 wt.%), preferably from 3 wt.% to 13 wt.%, a chlorinated polyolefin based terpolymer; and c) from 35 wt.% to 65 wt.%, preferably from 40 wt.% to 60 wt.%, most preferably from 45 wt.% to 60 wt.%, a filler.

In some embodiments, the coating composition of the present invention further comprises from 0.1 wt.% to 25 wt.%, preferably from 5 wt.% to 20 wt.%, most preferably from 10 wt.%) to 15 wt.%, a cured epoxy compound II;

Examples

I. Raw materials

TABLE 1

II. Test procedures

Overcoat window was determined by cross hatch tape test according to ASTM D3359-02 following the assessment protocol as:

a)Apply coatings onto Q-panels at a wet film thickness of 200um;

b) Allow each coating to achieve a tack free state;

c) Age coatings under natural light for a set period (lday to 6 months);

d) Top coat with acrylic surface coat at a wet film thickness of 200um;

e) Cure at room temperature for at least 5 days;

f) Subj ect to the cross hatch tape test;

The definition of the overcoat window:

The overcoat window was determined by the adhesion test result by cross hatch tape test. The different classifications of cross hatch tape test were listed in Table 2. Overcoat window was determined when the adhesion between top coat and primer begin to decrease from 5B to 4B.

TABLE 2 Cross Hatch Tape Test (ASTM D3359-02)

Chemical resistance test and salt spray resistance test were also conducted to evaluate anti- corrosion performance.

Chemical resistance test:

Tampons were stained with 10 wt. % sodium hydroxide solution or 10 wt. % sulfuric acid solution and put onto coating surface for different days. Plastic bottles were used to cover up the health cottons with chemicals to restrict water evaporation. Four rate scales were used: E: Excellent G: Good F: Fair P: Poor

TABLE 3 Standard test method for evaluating degree of blistering of paints (ASTM D714-

02), 5% NaCl salt spray test.

Rust Percent of surface rusted Visual Examples

Grade Spot(s) General(G) Pinpoint(P)

10 Less than or equal to 0.01 percent

9 Greater than 0.01 percent and up to 0.03 9-S 9-G 9-P percent

8 Greater than 0.03 percent and up to 0.1 8-S 8-G 8-P percent

7 Greater than 0.1 percent and up to 0.3 7-S 7-G 7-P percent

6 Greater than 0.3 percent and up to 1.0 6-S 6-G 6-P percent

5 Greater than 0.01 percent and up to 0.03 5-S 5-G 5-P percent

4 Greater than 3.0 percent and up to 10.0 4-S 4-G 4-P percent

3 Greater than 10.0 percent and up to 16.0 3-S 3-G 3-P percent

2 Greater than 16.0 percent and up to 33.0 2-S 2-G 2-P percent

1 Greater than 33.0 percent and up to 50.0 1-S 1-G 1-P percent

0 Greater than 50.0 percent None

III. Examples Primers were prepared according to the formulation listed in Table 4. Solid content is 77%, the epoxide group content is 1.145mmol/g.

TABLE 4 Primer formulations

N-butanol (solvent) 1.42

Titanium Dioxide Universal (filler) 2.30

D.E.R. 337-X-80 (epoxy) 5.83

Mica (filler) 5.38

D.E.R. 331 (epoxy) 11.57

Barium sulphate (filler) 14.17

Silica powder (filler) 21.47

Example 1

Primers were prepared according to the formulation listed in Table 1. Solid content is 77%. Charged 15g primer (77% solid) and 0.75g CONVINYL ^® G-75 (vinyl chloride/ vinyl acetate/ vinyl alcohol copolymer, 50% solid, Mn=32000, Vac content 4%, Hydroxyl value 75, Connell Bros. Company LTD.) and 6.67g phenalkamine curing agent, stirred for lOminutes. The thoroughly mixed solution was removed from the mixer and allowed to stay static for 2-5 minutes to remove gas bubbles. The above formulation was coated using blade coater on a Q- panel. A wet coating with a thickness of 200μπι was applied to clean Q-panels (H. J. Unkel LTD. Company). The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance.

Example 2 15g Primer (77% solid) and 1.5g CONVINYL ^® G-75 (vinyl chloride/ vinyl acetate/ vinyl alcohol copolymer, 50% solid, Mn=32000, Vac content 4%, Hydroxyl value 75, Connell Bros. Company LTD.) and 6.67g phenalkamine curing agent were charged. The preparing process is the same as in Example 1. The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance.

Example 3 15g Primer (77% solid) and 3g CONVINYL* G-75 (vinyl chloride/ vinyl acetate/ vinyl alcohol copolymer, 50% solid, Mn=32000, Vac content 4%, Hydroxyl value 75, Connell Bros. Company LTD.) and 6.67g phenalkamine curing agent were charged. The preparing process is the same as in Example 1. The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance.

Example 4

15g Primer (77% solid) and 1.5g CONVINYL ^® C-47 (chloride/ vinyl acetate/ maleic acid terpolymer, 50% solid, Mn=29000, Vac: Vcm: Mai = 13 : 86: 1, Connell Bros. Company LTD.) and 6.67g phenalkamine curing agent were charged. The preparing process is the same as in Example 1. The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance.

Example 5

15g Primer (77% solid) and 3g CONVINYL ^® C-47 (chloride/ vinyl acetate/ maleic acid terpolymer, 50% solid, Mn=29000, Vac: Vcm: Mai = 13 : 86: 1, Connell Bros. Company LTD.) and 6.67g phenalkamine curing agent were charged. The preparing process is the same as in Example 1. The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance.

Comparative Example 1 15g Primer (77% solid) and 6.67g phenalkamine curing agent were charged. The preparing process is the same as in Example 1. The coated panels were allowed to dry at room temperature for a set period prior to coating with top coat. Cross hatch tape test was conducted when top coat was completely dried. Salt spray test and chemical resistance test were also conducted to evaluate the anti-corrosion performance. Comparative Example 2

15g Primer (77% solid) and 0.75g poly( vinyl chloride) (average Mn=30000) and 6.67g phenalkamine curing agent, mixed and stirred for 30minutes. However, vinyl chloride was difficult to be completely dissolved with xylene, even after adding some methyl ethyl ketone into the primer system. So it has solubility issue for directly mixing poly(vinyl chloride) powder mixed into epoxy system.

IV. Results

TABLE 4 Coating properties from the examples

Table 4 summarizes the properties of various coatings used in this research. With the blending of vinyl chloride/ vinyl acetate/ vinyl alcohol copolymer CONVINYL ^® G-75 or vinyl chloride/ vinyl acetate/ maleic acid terpolymer CONVINYL ^® C-47, all the coatings have improved overcoatability windows and slightly improved anti-corrosion properties and chemical resistance ability. Glass transition temperature (Tg) of vinyl chloride polymer modified primers decreased a little comparing to that of comparative example 1. The impact resistance, Pendulum hardness and contact angles of the coatings cured for 30 days at room temperature were tested. These parameters vary with different dosages and are acceptable.