US20040211678A1 - Cathodic corrosion protection powder coating composition and method - Google Patents

Cathodic corrosion protection powder coating composition and method Download PDF

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Publication number
US20040211678A1
US20040211678A1 US10/424,891 US42489103A US2004211678A1 US 20040211678 A1 US20040211678 A1 US 20040211678A1 US 42489103 A US42489103 A US 42489103A US 2004211678 A1 US2004211678 A1 US 2004211678A1
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coating composition
weight
epoxy
curing
zinc borate
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US10/424,891
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English (en)
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Stephen Edmondson
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EIDP Inc
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Individual
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Priority to US10/424,891 priority Critical patent/US20040211678A1/en
Assigned to E. I. DU PONT DE NEMOURS AND COMPANY reassignment E. I. DU PONT DE NEMOURS AND COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: EDMONDSON, STEPHEN J.
Priority to PL378409A priority patent/PL378409A1/pl
Priority to PCT/US2004/013698 priority patent/WO2004096926A1/en
Priority to CNA2004800113324A priority patent/CN1780884A/zh
Priority to CA2522907A priority patent/CA2522907C/en
Priority to US10/546,487 priority patent/US7183346B2/en
Priority to EP04760468.1A priority patent/EP1618156B1/en
Priority to AU2004235402A priority patent/AU2004235402B2/en
Priority to MXPA05011528A priority patent/MXPA05011528A/es
Priority to RU2005136870/04A priority patent/RU2351623C2/ru
Priority to BRPI0410526-5A priority patent/BRPI0410526A/pt
Publication of US20040211678A1 publication Critical patent/US20040211678A1/en
Priority to NO20055567A priority patent/NO332830B1/no
Assigned to BARCLAYS BANK PLC, AS COLLATERAL AGENT reassignment BARCLAYS BANK PLC, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: U.S. COATINGS IP CO. LLC
Assigned to WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT reassignment WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: U.S. COATINGS IP CO. LLC (N/K/A AXALTA COATING SYSTEMS IP CO. LLC)
Assigned to AXALTA COATING SYSTEMS IP CO. LLC (FORMERLY KNOWN AS U.S. COATINGS IP CO. LLC) reassignment AXALTA COATING SYSTEMS IP CO. LLC (FORMERLY KNOWN AS U.S. COATINGS IP CO. LLC) RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/03—Powdery paints
    • C09D5/033—Powdery paints characterised by the additives
    • C09D5/038—Anticorrosion agents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08—Anti-corrosive paints
    • C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
    • C09D5/084—Inorganic compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/38—Boron-containing compounds

Definitions

  • the present invention is directed to a cathodic corrosion protection composition and method.
  • this invention is directed to a curable powder coating composition comprising zinc borate and a method for applying the coating composition, which when applied onto a steel, or other ferrous substrate, provides an anticorrosive coating, effective for improving resistance to cathodic disbandment.
  • cathodic protection prevents dissolution of steel by maintaining a steel material as a cathode and inhibiting ionization of iron.
  • the steel material is not generally used directly for a cathodic protection, but in most cases, a cathodic protection is effected in combination with an organic coating and/or lining.
  • 55-142063 discloses a composition consisting of a polyvinyl butyral resin, a liquid epoxide resin, a borate compound, an epoxy-silane coupling agent and phosphoric acid as a pre-treatment composition for baking type.
  • this coating composition is directed to a wash primer for pre-treating a metal and is different from the object of the present invention, and the resins used in this reference do not use a curing agent and are thermoplastic resins.
  • the present invention provides a curable cathodic corrosion protection coating, preferably a powder coating, in which the coating comprises:
  • thermosetting resin or mixture of thermosetting resins
  • the present invention further provides a method of cathodic corrosion protection which includes the steps of subjecting the substrate to a mechanical treatment, applying to said treated steel surface the cathodic protective coating, and polarizing the coated material as a cathode.
  • FIG. 1 is a graph illustrating the cathodic disbondment resistance correlation with zinc borate concentration.
  • the present invention is based upon the discovery that incorporation of low levels (additive quantities) of a zinc borate compound into a thermosetting resin based coating system, preferably a powder coating system, and applying this finish to a steel substrate, provides a coating which has excellent resistance to cathodic disbanding, especially in long term high temperature and humidity conditions.
  • the coating, and method of use thereof, of the present invention is useful as a coating for steel substrates, including for example, but not limited to, the internal and external surfaces of steel pipes, structural steel used in concrete, storage tanks, structural steel in marine environments, and oil production tubing and casings.
  • thermosetting resin in the coating composition of the present invention, any thermosetting resin can be used so long as it can firmly adhere to a steel material or to a steel material subjected to a mechanical treatment such as blast cleaning or to a steel material subjected to a chemical treatment such as a chromate treatment or treatment with zinc phosphate.
  • resins include an epoxy resin with an epoxy resin curing agent, a polyol resin with isocyanates, an acryl modified epoxy resin with a polymerization initiator, an alkyd resin, a humidity curing urethane resin, and so forth.
  • the thermosetting resin is an epoxy resin. More preferably the thermosetting resin is an epoxy resin, or mixtures of epoxy resins, used in conjunction with an effective epoxy curing agent.
  • the coating composition of the present invention preferably contains about 25 to 90% by weight, based upon total solids weight, of a thermosetting resin, or any mixture of thermosetting resins. More preferably, the composition contains about 60 to 80% by weight, based upon total solids weight, thermosetting resin, or mixtures thereof.
  • Examples of epoxy thermosetting resins suitable for the present invention are di-glycidyl ethers of 4,4-(bishydroxyphenyl) alkanes prepared by reacting 4,4′-(bishydroxyphenyl) alkanes such as bisphenol A, bisphenol F, bisphenol AD, etc., with epihalohydrin.
  • 4,4′-(bishydroxyphenyl) alkanes such as bisphenol A, bisphenol F, bisphenol AD, etc.
  • Epoxy resins of this kind are commercially available on the market as “EPON” and “EPIKOTE” (both are products of Resolution Performance Products, LLC.), “EPOTOHTO” (a product of Tohto Kasei K.K.), “ARALDITE” (a product of Vantico), “EPICLON” (a product of Dainippon Ink & Chemicals, Inc.), “Dow Epoxy” (a product of Dow Chemical International, Ltd.), and so forth.
  • a particularly useful epoxy is “EPON” 2024 bisphenol A/epichlorohydrin thermosetting epoxy resin, available from of Resolution Performance Products, LLC.
  • the coating composition of the present invention also contains a curing agent, or mixture of curing agents, incorporated in an amount effective to cure the coating.
  • a curing agent or mixture of curing agents, incorporated in an amount effective to cure the coating.
  • the coating contains about 1 to 35% by weight, based upon total solids weight, of a curing agent, or any mixture of curing agents. More preferably, the composition contains about 2 to 20% by weight, based upon total solids weight of a curing agent, or mixtures thereof.
  • epoxy curing agents for epoxy resins containing a plurality of addition-polymerizable functional groups to the epoxy group of an epoxy resin in the molecules thereof can be used as the epoxy curing agent.
  • the epoxy curing agents of this kind include diamines such as aliphatic diamines, aromatic diamine and heterocyclic diamines, various modified products of these diamines, polyamide resins obtained by the reaction with aliphatic acids and their dimers, acid anhydrides, thiols, phenols, and so forth.
  • the curing agents may be accelerated dicyandiamides having addition reactivity and self-polyaddition catalytic activity between epoxy groups, the derivatives thereof, and imidazoles.
  • epoxy resin curing agents are appropriately selected and used in accordance with the types of the coating, the curing conditions (ordinary temperature curing, heat curing, etc.), and so forth.
  • a particularly useful epoxy curing agent is “EPIKURE” P104, an accelerated dicyandiamide, available from Resolution Performance Products, LLC.
  • thermosetting curing system comprises a polyol resin and an isocyanate curing agent
  • urethane bonds also known as carbamate bonds
  • the polyol resin are polyol resins obtained by conventional preparation methods, such as polyester polyols, acrylic polyols, polyether polyols, etc., and these polyol resins are used either alone or in mixture of two or more polyols.
  • polyol diisocyanate adducts prepared by adding an equimolar diisocyanate to the number of hydroxyl groups of polyhydric alcohol compound and diisocyanate polymers obtained through self-polyaddition by reacting water with diisocyanates.
  • thermosetting resin comprises an acryl modified epoxy resin
  • such resin is formed by introducing a polymerizable double bond into the epoxy group of the epoxy resin by the addition reaction of acrylic acid
  • the epoxy resins having various grades are commercially available.
  • These acryl modified epoxy resins can be polymerized by radical polymerization, and can be cured by the use of a catalyst such as an organic peroxide, a photo-polymerization initiator, etc., as the polymerization initiator.
  • polyhydric alcohols as the starting material of the alkyd resin includes dihydric alcohols such as ethylene glycol, propylene glycol, 1,3-butylene glycol, 1,6-hexane diol, diethylene glycol, dipropylene glycol, neopentyl glycol, triethylene glycol, hydrogenated bis-phenol A, bis-phenol dihydroxypropyl ether, etc.; trihydric alcohols such as glycerin, trimethylolpropane, tris-hydroxymethyl aminomethane, etc.; and tetrahydric alcohols such as pentaerythrit, dipentaerythrit, etc.
  • dihydric alcohols such as ethylene glycol, propylene glycol, 1,3-butylene glycol, 1,6-hexane diol, diethylene glycol, dipropylene glycol, neopentyl glycol, triethylene glycol, hydrogenated bis-phenol A, bis-phenol dihydroxypropyl ether, etc.
  • polyvalent carboxylic acids include dibasic acids such as phthalic anhydride, isophthalic acid, terephthalic acid, succinic anhydride, adipic acid, azelaic acid, sebacic acid, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, tetrabromophthalic anhydride, tetrachlorophthalic anhydride, endomethylene tetrahydrophthalic anhydride, maleic anhydride, fumaric anhydride, itaconic acid, etc.; tribasic acids such as trimellitic anhydride, methylcyclohexenetricarboxylic acid, etc.; and tetrabasic acids such as pyromellitic anhydride.
  • dibasic acids such as phthalic anhydride, isophthalic acid, terephthalic acid, succinic anhydride, adipic acid, azelaic acid, sebacic acid, tetra
  • aliphatic acids examples include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, ricinoleic acid, linolenic acid, eleostearic acid, and so forth.
  • the alkyd resins synthesized from the polyhydric alcohols, the polybasic acids and the aliphatic acids described above are used, but in many cases, they are used after being subjected to various modification treatments.
  • the modified resins include phenol-alkyd resins obtained by adding phenols to the alkyd resin and having improved chemical resistance and adhesion to the steel material, bisphenol type epoxy resins, epoxy-modified alkyd resins obtained by adding alicyclic or aliphatic epoxy compounds (the resin of this type are sometimes referred to as the “epoxypolyester resins”) and vinylalkyd resins obtained by adding styrene, vinyltoluene, acrylic acid esters or methacrylic acid esters.
  • Curing of these various kinds of alkyd resins can be made by a melamine resin or a urea resin. They can be cured by oxidation in air using organometallic salts such as an organic acid with lead, manganese, cobalt, etc. In the present invention, these alkyd resins can be selected optionally in order to satisfy performance other than the cathodic disbonding resistance, and the applicability of coating.
  • humidity curing urethane resin means those resins which are prepared by synthesizing a resin having an isocyanate group left at the terminal thereof by reacting an isocyanate in excess with a polyol resin and a polyhydric alcohol and reacting and curing the isocyanate groups between the resins by the moisture in air.
  • the present invention may use a phenoxy resin.
  • the phenoxy resin is an epoxy resin which is derived from bisphenol and has an extremely large molecular weight. The number average molecular weight thereof is at least 10,000 and the number of epoxy groups is extremely small. Examples of commercially available phenoxy resins are “DER684” (a product of Dow Chemical), “EPOTOHTO YD050” and “EPOTOHTO YD040” (products of Tohoto Kasei K.K.).
  • the ratio of the curing agent/reactive resin component of the coating solution is preferably (0.6-1.1)/1.0, more preferably (0.8-1.0)/1.0, in terms of the equivalent ratio of the reactive group of the curing agent and the functional groups capable of reacting with the reactive group of the curing agent.
  • the coating composition of the present invention further comprises a zinc borate compound.
  • the zinc borate compound promotes disbondment resistance by reducing conversion of the steel substrate. The effect is most noticeable in long term severe exposure tests, such as 28 day cathodic disbandment tests at elevated temperatures (e.g. 80° C.), where the zinc borate compound can reduce disbonding by 50%.
  • the zinc borate compound is added at low levels below 5% by weight, based on total solids, preferably from about 0.5-4.75%, more preferably 0.5-4.0%, and even more preferably 1.5-2.5%. By using such amounts, the disbondment is significantly reduced. Further, use of these low levels of zinc borate compounds provides a significant decrease in cost, as it is commonly known that such zinc compounds are more expensive than thermosetting resin systems. Also, issues of zinc compound solubility, over long periods of time, are improved when low levels are used.
  • the zinc borate compound constituting the anticorrosive coating composition of the present invention may comprise an individual zinc borate compound, or a mixture of two or more zinc borate compounds.
  • Examples of such zinc borate compound include, but are not limited to, zinc methaborate [Zn(BO 2 ) 2 ], basic zinc borate [ZnB 4 O 7 .2ZnO] and zinc borate [2ZnO.3B 2 O 3 .3.5H 2 O].
  • Zinc borate is preferably used.
  • Zinc borate can be obtained by melting a mixed starting material of zinc oxide and boric acid or double-decomposing the aqueous solution of the mixed starting material.
  • a particularly useful zinc borate compound is “Borogard ZB fine,” [2ZnO.3B 2 O 3 .3.5H 2 O], available from U.S. Borax, Incorporated.
  • the coating compositions of the present invention may additionally comprise one or more components taken, for example, from the group consisting of pigments, dyes, fillers, flow control agents, dispersants, thixotropic agents, adhesion promoters, antioxidants, light stabilizers and curing catalysts. They may also include other known anticorrosion agents, for example anticorrosion pigments, such as phosphate- or containing pigments, metal oxide pigments, for example calcium oxide or combined calcium oxide/silica pigments, or other organic or inorganic corrosion inhibitors, for example salts of nitroisophthalic acid, phosphoric esters, technical-grade amines or substituted benzotriazoles.
  • anticorrosion pigments such as phosphate- or containing pigments
  • metal oxide pigments for example calcium oxide or combined calcium oxide/silica pigments
  • organic or inorganic corrosion inhibitors for example salts of nitroisophthalic acid, phosphoric esters, technical-grade amines or substituted benzotriazoles.
  • the pigments are, for example, titanium dioxide, iron oxide, aluminum bronze or phthalocyanine blue.
  • fillers are talc, alumina, aluminum silicate, barytes, mica, and silica.
  • the corrosion inhibitors can be applied to a support material. Pulverulent fillers or pigments are particularly suitable for this purpose.
  • the coating composition of the present invention contains from 0 to 55% by weight, more preferably 5 to 30% by weight, based upon total solids weight, of fill temperature to minimize any curing and gelation from taking place in the extruder.
  • the extruded composition usually in sheet form after cooling, is broken into chips and then ground in a mill to a powder and subsequently screened to achieve the desired powder particle size.
  • the aforesaid curable powder coating composition of the present invention exhibits superior adhesive properties, as demonstrated by having superior resistance to cathodic disbondment, over an extended period, together with very rapid cure speeds. These properties provide a powder coating that can be readily applied, by typical application means in the powder coating art, to rebars, pipelines and other metallic substrates, some of which may require cold working after being coated.
  • the superior adhesive properties of this invention provide the ability to adhere to even oily an scaly surfaces, such as those encountered on steel strappings and other marginally clean metallic substrates.
  • the cure time/temperature range of the aforementioned powder coating composition of this invention is found to be from about 60 seconds at about 470° F. to about 180 seconds at about 400° F.
  • the metal substrate is preheated to a temperature from about 400° F. to 490° F. Then, the powder coating is applied by standard means, such as fluidized bed immersion, electrostatic spray application, and the like. The residual heat in the preheated metal substrate provides enables the powder coating finish to melt, flow and begin to cure to a continuous, anticorrosive, dry film.
  • the aforesaid powder coated metal substrate may then be introduced into high temperature ovens, such as convection, infrared, or combination ovens, to melt, flow out and further cure into a smooth hardened film.
  • high temperature ovens such as convection, infrared, or combination ovens
  • the melt flow and cure time usually ranges between about 40 and 140 seconds at a peak substrate temperature ranging between about 400° F. and 490° F.
  • the coated substrate is conveyed to a water quench to lower the temperature to between about 100° F. and 200° F.
  • Steel substrates are usually coated with an effective amount of powder coating to produce a dry film thickness of between about 5 and 20 mils thick or greater.
  • the anticorrosive coating composition having the composition described above can be produced by the same method as the production methods of ordinary coating compositions.
  • a predetermined amount of the zinc borate compound is added to the thermosetting resin, and the mixture is subjected to dispersion treatment using a roll mill, a dissolver, etc.
  • an organic solvent type coating composition the mixture is subjected to dispersion treatment using a roll mill, a dissolver, an SG mill, a pot mill, etc.
  • a predetermined amount of the zinc borate compound is added to the thermosetting resin, and the mixture is premixed, then heat-kneaded, cooled, and thereafter pulverized and classified.
  • the present invention likewise relates to a process for preparing a corrosion-resistant surface coating on a corrodable metal surface, which comprises treating this surface with the coating composition of the present invention.
  • the coating of the anticorrosive coating method according to the present invention is applied by the use of a brush, a roller, an airless spray, an air spray, a powder coating mechanism, etc., which is selected suitably in accordance with the form of the composition, in a customary manner.
  • a heavy duty protective film such as polyethylene lining, heavy duty protective urethane coating composition, epoxy resin coating composition, and the like, and/or a finishing layer such as a coloring layer may be applied to the surface of the coating film after it is coated.
  • a voltage of 1.5V was applied across the Platinum wire and the test panel. After 28 days in the oven, the panels were tested for disbandment by removing the solution and cylinder then making 8 radial cuts in the coating away from the holiday. The panel was left for one hour to cool to room temperature then the coating was removed with a knife by working away from the holiday edge using a levering action. The disbandment from the center of the holiday to edge of the disbanded area was measured, then averaged. This method follows TransCanada Pipeline spec. TESCOAT FBE Rev.0, which is based on CSA Z245.20-98.
  • Table 1 illustrates the preparation of cathodic disbondment resistant thermosetting epoxy powder coating compositions, of the present invention, having zinc borate levels varied progressively from 4.9% down to 0%, that are suitable for fusion coating on rebars, pipelines, and other metallic substrates.
  • the epoxy curing agent is an accelerated dicyandiamide type curing agent. All amounts are given in percent by weight of total formulation weight.
  • Table 3 illustrates the preparation of a cathodic disbandment resistant thermosetting epoxy powder coating composition, of the present invention having zinc borate level of 3% and a phenolic type curing agent. All amounts are given in percent by weight of total formulation weight.
  • TABLE 3 Ingredient Example 6 Epon TM 2024 epoxy resin (Resolution 55 Performance Products, LLC.) Epikure TM P202 phenolic epoxy curing agent 11 (Resolution Performance Products, LLC.) Zinc Borate (Borogard TM ZB, US Borax, Inc.) 3 Nyad TM M400 filler (NYCO Minerals, Inc.) 29.7 Bayferrox TM 140 iron oxide pigment (Bayer 1 Corp.) Cabosil TM M5 (Cabot, Inc.) 0.3
  • Example 6 listed in Table 3, was then coated on steel panels, cured, and subjected to long term performance tests, as described above.
  • the resultant coating yielded a 20.8 mm disbandment measurement, over the 28 day, 80° C., long term disbandment test.

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US10/424,891 2003-04-28 2003-04-28 Cathodic corrosion protection powder coating composition and method Abandoned US20040211678A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
US10/424,891 US20040211678A1 (en) 2003-04-28 2003-04-28 Cathodic corrosion protection powder coating composition and method
BRPI0410526-5A BRPI0410526A (pt) 2003-04-28 2004-04-28 composição de revestimento curável, composição de revestimento de epóxi em pó e método de proteção de cátodo
EP04760468.1A EP1618156B1 (en) 2003-04-28 2004-04-28 Cathodic corrosion protection powder coating composition and method
MXPA05011528A MXPA05011528A (es) 2003-04-28 2004-04-28 Metodo y composicion de recubrimiento de polvo de proteccion contra la corrosion catodica.
CNA2004800113324A CN1780884A (zh) 2003-04-28 2004-04-28 阴极腐蚀防护粉末涂料组合物和方法
CA2522907A CA2522907C (en) 2003-04-28 2004-04-28 Cathodic corrosion protection powder coating composition and method
US10/546,487 US7183346B2 (en) 2003-04-28 2004-04-28 Cathodic corrosion protection powder coating composition and method
PL378409A PL378409A1 (pl) 2003-04-28 2004-04-28 Proszkowa kompozycja powłokowa i sposób ochrony przed korozją katodową
AU2004235402A AU2004235402B2 (en) 2003-04-28 2004-04-28 Method of cathode protection
PCT/US2004/013698 WO2004096926A1 (en) 2003-04-28 2004-04-28 Cathodic corrosion protection powder coating composition and method
RU2005136870/04A RU2351623C2 (ru) 2003-04-28 2004-04-28 Состав порошкового покрытия для катодной защиты от коррозии и способ
NO20055567A NO332830B1 (no) 2003-04-28 2005-11-24 Fremgangsmate for katodebeskyttelse av et stalmateriale

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EP (1) EP1618156B1 (es)
CN (1) CN1780884A (es)
AU (1) AU2004235402B2 (es)
BR (1) BRPI0410526A (es)
CA (1) CA2522907C (es)
MX (1) MXPA05011528A (es)
NO (1) NO332830B1 (es)
PL (1) PL378409A1 (es)
RU (1) RU2351623C2 (es)
WO (1) WO2004096926A1 (es)

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US20050075430A1 (en) * 2003-09-05 2005-04-07 Edmondson Stephen J. Curable alkanolamine containing epoxy powder coating composition
US20060272909A1 (en) * 2005-06-02 2006-12-07 Fuller Brian K Brake assembly and coating
US20070293614A1 (en) * 2006-06-15 2007-12-20 Zhou Wenjing J Powder coating composition for pipe coating
US20080001240A1 (en) * 2006-06-30 2008-01-03 Masanori Minamio Solid state image pickup device, method for manufacturing the same, semiconductor device and method for manufacturing the same
EP2199314A1 (en) * 2008-12-19 2010-06-23 Hexion Specialty Chemicals Research Belgium S.A. Powder coating compositions for low temperature curing and high flow
US20100175354A1 (en) * 2008-02-22 2010-07-15 Yoshikatsu Mizukami Polymer composition and molded products formed thereof
US20110244211A1 (en) * 2008-12-09 2011-10-06 Societe Civile De Brevets Matiere Method for producing a reinforced concrete part, and thus-produced part
CN106193466A (zh) * 2016-08-10 2016-12-07 江苏溧阳建设集团有限公司 一种建筑屋顶防水层
CN110713774A (zh) * 2019-09-27 2020-01-21 洛阳双瑞防腐工程技术有限公司 一种高韧性低温快速固化重防腐环氧粉末涂料及其制备方法
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CN110713774A (zh) * 2019-09-27 2020-01-21 洛阳双瑞防腐工程技术有限公司 一种高韧性低温快速固化重防腐环氧粉末涂料及其制备方法
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NO332830B1 (no) 2013-01-21
US7183346B2 (en) 2007-02-27
CN1780884A (zh) 2006-05-31
PL378409A1 (pl) 2006-04-03
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US20060167155A1 (en) 2006-07-27
EP1618156A1 (en) 2006-01-25
CA2522907A1 (en) 2004-11-11
EP1618156B1 (en) 2013-11-27
AU2004235402B2 (en) 2008-08-21
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BRPI0410526A (pt) 2006-06-20
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