WO2019146583A1 - Anti-rust treatment solution for end face of plated steel sheet, method for chemical conversion treatment of end face of plated steel sheet, chemical conversion treated steel sheet, and molded article - Google Patents

Anti-rust treatment solution for end face of plated steel sheet, method for chemical conversion treatment of end face of plated steel sheet, chemical conversion treated steel sheet, and molded article Download PDF

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Publication number
WO2019146583A1
WO2019146583A1 PCT/JP2019/001820 JP2019001820W WO2019146583A1 WO 2019146583 A1 WO2019146583 A1 WO 2019146583A1 JP 2019001820 W JP2019001820 W JP 2019001820W WO 2019146583 A1 WO2019146583 A1 WO 2019146583A1
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Prior art keywords
chemical conversion
plated steel
group
face
steel sheet
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PCT/JP2019/001820
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French (fr)
Japanese (ja)
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雅典 松野
晋 上野
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日新製鋼株式会社
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Priority to CN201980009627.4A priority Critical patent/CN111630207B/en
Priority to KR1020207021391A priority patent/KR20200110751A/en
Publication of WO2019146583A1 publication Critical patent/WO2019146583A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/14Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies
    • B05D7/16Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies using synthetic lacquers or varnishes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B32B15/082Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising vinyl resins; comprising acrylic resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08Anti-corrosive paints
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/60Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using alkaline aqueous solutions with pH greater than 8
    • C23C22/62Treatment of iron or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/68Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous solutions with pH between 6 and 8
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/16Acidic compositions
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/32Alkaline compositions
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2506/00Halogenated polymers
    • B05D2506/10Fluorinated polymers

Definitions

  • the present invention relates to an end face rustproofing solution for a plated steel plate, a method for forming a plated steel plate, a conversion-treated steel plate, and a shaped and processed product.
  • the said plated steel plate is used in many cases as a shaping
  • a chemical conversion treatment film is formed on the end face or exposed part Sometimes.
  • Patent Document 1 discloses, as a treatment liquid used for forming a chemical conversion film on an end face, a metal component selected from Ca, Mg, Mn and Zn which imparts corrosion resistance to the film, and phosphate ions and ethylene oxide which form the film.
  • a treatment liquid containing an organic compound having a group is described.
  • the ethylene oxide group of the organic compound is bonded to a phosphate ion to form a film of phosphoric acid ester, and the metal component in the film is an oxide or a hydroxide. It is supposed to be dispersed.
  • Patent Document 2 blocks water from the end face with magnesium dihydrogen phosphate, magnesium hydrogen phosphate or L-ascorbic acid as a rust inhibitor.
  • a processing solution containing silica fine particles as a binder component for the purpose is described.
  • Patent Document 3 discloses, as a corrosion inhibitor, unsaturated alcohols, saturated linear primary amines, saturated linear secondary amines, saturated straight chain An aqueous solution in which an organic corrosion inhibitor selected from chain tertiary amines, thioureas, phosphonic acids, morpholines and imidazolines is described.
  • Patent Document 4 is obtained by reacting esters of acrylic acid or methacrylic acid with a vinyl-based monomer such as styrene and vinyl acetate as another treatment liquid used for forming a chemical conversion treatment film on the end face.
  • An acrylic lacquer is described in which a copolymer resin or the like is incorporated therein.
  • the acrylic lacquer is applied so as to have a dry film thickness of 5 to 30 ⁇ m to form a film, whereby the end face is uniformly coated and a sufficient antirust action is exhibited. It is assumed.
  • Patent Document 5 describes an aqueous paint containing an aqueous urethane paint and a zinc powder for enhancing the coatability.
  • Patent Documents 6 to 10 disclose water resistance of organic resin film containing fluorine resin by crosslinking fluorine resin with a compound containing Group 4 metal. The chemical conversion solution is described, which can enhance the
  • Patent Documents 1 to 3 have a problem that the action of suppressing the occurrence of red rust (antirust action) is not so high, and the antirust effect can not be maintained for a long time.
  • Patent Documents 6 to 10 when a chemical conversion treatment film is formed using a chemical conversion solution containing a fluorine resin and a Group 4 metal, a transparent film having excellent weather resistance can be formed. In addition, since the water resistance of the chemical conversion film can be enhanced by crosslinking of the fluorine resin, it is very useful.
  • the present invention is formed by an end face rustproofing treatment liquid capable of forming a chemical conversion treated film with higher corrosion resistance, a chemical conversion treatment method using the endface rustproofing treatment liquid, and the chemical conversion treating method
  • An object of the present invention is to provide a chemically treated steel sheet having a chemical conversion film and a shaped and processed product.
  • one aspect of the present invention relates to an end face rustproofing solution for chemical conversion treatment of a plated steel plate.
  • the above-mentioned end face rustproofing treatment liquid is an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms.
  • one or more bonding promoters selected from the group consisting of n-methyl-2-pyrrolidone and a silane coupling agent.
  • the other aspect of this invention is related with the chemical conversion treatment method of a plated steel plate.
  • the chemical conversion treatment method includes the step of applying an end surface rustproofing solution for chemical conversion treatment of the plated steel sheet to the end surface of the plated steel sheet.
  • the above-mentioned end face rustproofing treatment liquid is an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms.
  • one or more bonding promoters selected from the group consisting of n-methyl-2-pyrrolidone.
  • the further another aspect of this invention is related with the chemical conversion treatment steel plate which has a plated steel plate and the chemical conversion treatment film formed in the end surface of the said plated steel plate.
  • the chemical conversion film is an ester compound of an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms, and at least one bond promoter selected from the group consisting of n-methyl-2-pyrrolidone and a silane coupling agent.
  • the further another aspect of this invention relates to the shaping
  • the molded product includes a chemical conversion film formed on an end face of the plated steel sheet, and the chemical conversion film includes an organic resin containing a fluorine resin, a compound containing a Group 4 element, or an ion of a Group 4 element.
  • one or more bond promoters selected from the group consisting of adipic acid or an ester compound of phthalic acid and an alcohol having 1 to 3 carbon atoms, and n-methyl-2-pyrrolidone, and a silane coupling agent Including.
  • an end face rustproofing treatment liquid capable of forming a chemical conversion treatment film having higher corrosion resistance, a chemical conversion treatment method using the endface rustproofing treatment liquid, and a chemical conversion treated film formed by the chemical conversion treatment method
  • molding processed article are provided.
  • the inventors of the present invention as a result of intensive studies, have identified specific compounds (hereinafter simply referred to as “bond promoters” in an aqueous resin containing an organic resin containing a fluorine resin and a compound containing a Group 4 element or an ion of a Group 4 element. Furthermore, it was found that the corrosion resistance of the chemical conversion film formed on the end face of the plated steel plate is further enhanced by further containing a silane coupling agent to obtain an end face rustproofing solution.
  • the inventors of the present invention have further studied the action and effect of improving the corrosion resistance, and as a result, an ester compound of adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms as the bond promoter, and n-methyl-2 It has been found that pyrrolidone can be used, thus completing the present invention.
  • the above-mentioned bond promoter can soften the fluorocarbon resin which is usually present in the aqueous treatment liquid as an emulsion.
  • the fluororesin softened by the bonding promoter is more likely to be fused and forms a chemical conversion treated film having higher water resistance, so that it is considered that the weather resistance of the chemical conversion treated film is further enhanced.
  • the aqueous treatment liquid contains an organic resin containing a fluorocarbon resin, a compound containing a Group 4 element or an ion of a Group 4 element, and the bond promoter.
  • the aqueous processing solution may further contain other components such as an etching agent.
  • Organic resin is an organic resin containing a fluorocarbon resin.
  • the fluorine resin can enhance the weather resistance (such as ultraviolet light resistance and light resistance) and corrosion resistance (such as prevention of rust) of the chemical conversion film.
  • the organic resin may contain a resin other than the fluorocarbon resin as long as the weatherability and corrosion resistance of the chemical conversion film are not significantly reduced.
  • Fluororesins are roughly classified into solvent-based fluorocarbon resins and aqueous fluorocarbon resins. Among these, it is preferable to use a water-based fluorine resin which is easy to use for a water-based treatment liquid in which recovery of the volatilized solvent is not a problem.
  • the water-based fluorine resin means a fluorine resin having a hydrophilic functional group.
  • hydrophilic functional groups include carboxyl and sulfonic acid groups, salts thereof and the like.
  • salts of carboxyl groups or sulfonic acid groups include ammonium salts, amine salts, alkali metal salts and the like.
  • the water-based fluorine resin preferably has an amount of hydrophilic functional groups of 0.05% by mass to 5% by mass.
  • the fluorine resin in which the amount of the hydrophilic functional group is 0.05% by mass or more and 5% by mass or less can be made into an aqueous emulsion without using any emulsifying agent.
  • the chemical conversion film containing substantially no emulsifier can be a chemical conversion film excellent in water resistance.
  • the content of the hydrophilic functional group in the water-based fluorine resin may be determined by dividing the total molar mass of the hydrophilic functional group contained in the water-based fluorine resin by the number average molecular weight of the water-based fluorine resin.
  • the molar mass of the carboxyl group is 45, and the molar mass of the sulfonic acid group is 81. Therefore, the number of each of the carboxyl group and the sulfonic acid group contained in the aqueous fluorocarbon resin is determined, and each is multiplied by the molar mass to obtain an aqueous system.
  • the total molar mass of hydrophilic functional groups contained in the fluorocarbon resin is determined.
  • the number average molecular weight of the aqueous fluororesin can be measured by GPC.
  • the carboxyl group in the water-based fluorine resin forms a hydrogen bond or the like with the surface of the steel plate or plating layer (or base chemical conversion treatment film), and the adhesion between the chemical conversion treatment film and the steel plate or plating layer (or base chemical conversion treatment film) surface
  • H + is difficult to dissociate, a cross-linking reaction with a compound containing a Group 4 element or an ion of a Group 4 element hardly occurs.
  • the sulfonic acid group in the aqueous fluorocarbon resin is likely to cause a cross-linking reaction with a compound containing a Group 4 element or an ion of a Group 4 element because H + is easily dissociated, but a compound containing a Group 4 element Alternatively, if it remains unreacted in the film without undergoing a crosslinking reaction with ions of a Group 4 element, the water molecule adsorption is strong, which may significantly reduce the water resistance of the chemical conversion film. Therefore, in order to take advantage of the respective features, it is preferable that the aqueous fluororesin contain both a carboxyl group and a sulfonic acid group. In this case, the ratio of carboxyl group to sulfonic acid group is preferably in the range of 5 or more and 60 or less in terms of the molar ratio of carboxyl group / sulfonic acid group.
  • the number average molecular weight of the aqueous fluororesin is preferably 1,000 or more, more preferably 10,000 or more, and particularly preferably 200,000 or more.
  • the water permeability and water resistance of a chemical conversion treatment film can fully be improved as the lower limit of the number average molecular weight of water-based fluorine resin is the above value, and a plated steel sheet by moisture, corrosive gas, etc. penetrating a chemical conversion treatment film Corrosion can be suppressed.
  • the lower limit of the number average molecular weight of the water-based fluorine resin is the above value, radicals generated by the action of light energy and the like are less likely to act on the end of the polymer chain. It is also possible to suppress the deterioration of the chemical conversion coating due to being done.
  • the intermolecular force becomes strong, and the cohesion of the chemical conversion treatment film is enhanced, whereby the water resistance of the chemical conversion treatment film can be further enhanced.
  • the bond between atoms in the main chain of the water-based fluorine resin is stabilized, and the deterioration of the chemical conversion treatment film due to the hydrolysis of the water-based fluorine resin also hardly occurs.
  • the number average molecular weight of the aqueous fluororesin is preferably 2,000,000 or less.
  • the upper limit of the number average molecular weight of the water-based fluororesin is 2,000,000 or less, gelation of the water-based treatment liquid is unlikely to occur, and the storage stability of the water-based treatment liquid is further enhanced.
  • the water-based fluorine resin preferably contains 6 mass% or more of fluorine (F) atoms with respect to the total mass of the fluorine resin, from the viewpoint of further improving the weather resistance and corrosion resistance of the chemical conversion film, 8 mass% or more It is more preferable to include the (F) atom, and it is further preferable to include the fluorine (F) atom of 13% by mass or more. Further, from the viewpoint of facilitating the formation of a coating and improving the adhesion and drying properties of the chemical conversion film, the water-based fluorine resin has a fluorine (F) atom of 20% by mass or less based on the total mass of the fluorine resin. It is preferable to include.
  • the content of fluorine (F) atoms in the water-based fluorine resin can be measured by using a fluorescent X-ray analyzer.
  • the water-based fluorine resin is preferably a fluorine-containing olefin resin.
  • fluorine-containing olefin resins include copolymers of fluoroolefins and hydrophilic functional group-containing monomers.
  • fluoroolefins examples include tetrafluoroethylene, trifluoroethylene, chlorotrifluoroethylene, hexafluoropropylene, vinyl fluoride, vinylidene fluoride, pentafluoropropylene, 2,2,3,3-tetrafluoropropylene, 3 And 3,3,3-trifluoropropylene, bromotrifluoroethylene, 1-chloro-1,2-difluoroethylene, 1,1-dichloro-2,2-difluoroethylene and the like. These fluoroolefins may be used alone or in combination of two or more.
  • perfluoroolefins including tetrafluoroethylene and hexafluoropropylene, and vinylidene fluoride are preferable from the viewpoint of further enhancing the UV resistance.
  • the content of the fluoroolefin containing chlorine such as chlorotrifluoroethylene is preferably small (for example, 0.1 mol% or less) from the viewpoint of suppressing the corrosion by the chlorine ion.
  • hydrophilic functional group-containing monomer examples include known carboxyl group-containing monomers and sulfonic acid group-containing monomers. These hydrophilic functional group-containing monomers may be used alone or in combination of two or more.
  • Examples of the carboxyl group-containing monomer include unsaturated carboxylic acids represented by the following formula (1), and unsaturated carboxylic acids including their esters or acid anhydrides.
  • R 1 , R 2 and R 3 independently represent a hydrogen atom, an alkyl group, a carboxyl group or an ester group.
  • N is an integer of 0 to 20.
  • unsaturated carboxylic acid represented by the above formula (1) examples include acrylic acid, methacrylic acid, vinylacetic acid, crotonic acid, cinnamic acid, itaconic acid, itaconic acid monoester, maleic acid, maleic acid monoester, fumar Acid, fumaric acid monoester, 5-hexenoic acid, 5-heptenoic acid, 6-heptenoic acid, 7-octenoic acid, 8-nonenoic acid, 9-decenoic acid, 10-undecylenic acid, 11-dodecylenic acid, 17-octadecyrene Acids and oleic acid are included.
  • R 4 and R 5 independently represent a saturated or unsaturated linear or cyclic alkyl group, n is 0 or 1, and m is 0 or 1.
  • carboxyl group-containing vinyl ether monomer represented by the above formula (2) examples include 3- (2-allyloxyethoxycarbonyl) propionic acid, 3- (2-allyloxybutoxycarbonyl) propionic acid, 3- (2- And vinyloxyethoxycarbonyl) propionic acid, 3- (2-vinyloxybutoxycarbonyl) propionic acid and the like.
  • sulfonic acid group-containing monomer examples include vinyl sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, styrene sulfonic acid, 2-acrylamido-2-methylpropane sulfonic acid, 2-methacryloyloxyethane sulfonic acid, 3- Methacryloyloxypropane sulfonic acid, 4-methacryloyloxybutane sulfonic acid, 3-methacryloyloxy-2-hydroxypropane sulfonic acid, 3-acryloyloxypropane sulfonic acid, allyloxy benzene sulfo inic acid, methalyloxy benzene sulfonic acid, isoprene sulfone And acids and 3-allyloxy-2-hydroxypropane sulfonic acid.
  • the copolymer of the fluoroolefin and the hydrophilic functional group-containing monomer may be further copolymerized with another copolymerizable monomer, if necessary.
  • the other copolymerizable monomer include carboxylic acid vinyl esters, alkyl vinyl ethers and non-fluorinated olefins.
  • the carboxylic acid vinyl esters can improve the compatibility of the water-based fluorine resin and the gloss of the chemical conversion film, and can increase the glass transition temperature.
  • Examples of the above-mentioned vinyl carboxylates include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl isobutyrate, vinyl pivalate, vinyl caproate, vinyl versatate, vinyl laurate, vinyl stearate, vinyl cyclohexylcarboxylate, Vinyl benzoate and vinyl para-t-butyl benzoate and the like are included.
  • the alkyl vinyl ethers can improve the gloss and the flexibility of the chemical conversion film.
  • Examples of the above alkyl vinyl ethers include methyl vinyl ether, ethyl vinyl ether, butyl vinyl ether and the like.
  • the non-fluorinated olefins can improve the flexibility of the chemical conversion film.
  • Examples of the non-fluorinated olefins include ethylene, propylene, n-butene, and isobutene.
  • an emulsion of a fluoroolefin copolymer having a hydrophilic functional group can be obtained by copolymerizing the above-described monomers by an emulsion polymerization method. At this time, most of the emulsifier is used by adjusting the amount of fluoroolefin in the raw material monomer composition such that the fluoroolefin copolymer has a hydrophilic functional group in an amount of 0.05% by mass to 5% by mass.
  • An aqueous emulsion of a fluoroolefin copolymer can be produced without.
  • the fluorine resin produced by the method as described above is considered to exist in the form of particles in the aqueous treatment liquid.
  • the average particle size of the fluororesin emulsion is preferably 50 nm or more and 300 nm or less.
  • the storage stability of the aqueous treatment liquid can be enhanced by setting the average particle size of the emulsion to 50 nm or more.
  • the average particle diameter of the emulsion can be brought into the above range by optimizing the shear rate and the stirring time.
  • the content of the fluorine resin in the aqueous treatment liquid is preferably 10 parts by mass or more and 70 parts by mass or less with respect to 100 parts by mass of water.
  • the content of the fluorine resin is 10 parts by mass or more, the film formability and the compactness of the chemical conversion film are less likely to be lowered by evaporation of a large amount of water in the drying process.
  • the content of the fluorine resin is 70 parts by mass or less, the storage stability of the aqueous treatment liquid is further enhanced.
  • the content of the fluorine resin in the aqueous treatment liquid is preferably 70% by mass or more and 99% by mass or less with respect to the total amount of the solid content (component excluding water and other solvents).
  • Compound containing Group 4 element or ion of Group 4 element is a fluorine resin, in particular, a functional group such as a carboxyl group or a sulfonic acid group in a water-based fluorine resin It easily reacts with water, and promotes the curing or crosslinking reaction of the water-based fluorocarbon resin. Therefore, the compound of the Group 4 element or the ion of the Group 4 element can improve the adhesion of the fluorine resin, and improve the water resistance of the chemical conversion film even at low temperature drying.
  • Compounds containing Group 4 elements include oxyacids, fluorides, hydroxides, organic acid salts, carbonates, peroxides, ammonium salts, alkali metal salts, and alkaline earth metal salts of Group 4A metals. can do.
  • the oxy acid salt means a salt with an acid having carbon and another element (such as carbonic acid or sulfuric acid).
  • Examples of oxy acid salts include hydrogen salts, carbonates, sulfates and the like.
  • Examples of ions of the Group 4 element include ions of the Group 4 element derived from the above compounds.
  • Examples of the compound containing a Group 4 element or the ion of a Group 4 element include titanium (Ti) compounds, zirconium (Zr) compounds and hafnium (Hf) compounds.
  • Ti titanium
  • Zr zirconium
  • Hf hafnium
  • a zirconium compound is preferable from the viewpoint of suppressing a decrease in weatherability due to a photocatalyst described later.
  • a compound containing a Group 4 element or an ion of a Group 4 element is less likely to cause weathering deterioration of a chemical conversion treatment film due to oxidation or hydrolysis of an ester bond or a formal ether bond.
  • the compound containing a Group 4 element or the ion of a Group 4 element is a chemical conversion treated film in which the cross-linked structure is cut by an acidic substance such as sulfate ion or nitrate ion contained in acid rain. It is hard to produce the weathering deterioration of.
  • the compound of the Group 4 element or the ion of the Group 4 element crosslinks the fluorine resin with a stronger bonding force than the urethane bond formed in the cross-linked portion using the isocyanate resin, the weathering by cutting the cross-linked structure Progress of deterioration is less likely to occur.
  • the compound containing a Group 4 element or the ion of a Group 4 element also improves the film adhesion, the water resistance and the color fastness of the chemical conversion film.
  • a chemical conversion treatment film is formed on the surface of an Al-containing Zn-based alloy plated steel sheet with an aqueous treatment liquid containing a compound containing a Group 4 element or an ion of a Group 4 element, strong Al present on the surface of the plated steel sheet It is possible to suppress the decrease in the film adhesion due to the oxide.
  • the content of the compound containing a Group 4 element or the ion of a Group 4 element in the aqueous treatment liquid in terms of metal atom can be, for example, 0.5 g / L, but the aqueous fluororesin is sufficiently crosslinked. It is preferable that it is 2 g / L or more from a viewpoint of improving the adhesiveness of a chemical conversion treatment film more. From the above viewpoint, the content of the ion of the compound containing the Group 4 element or the Group 4 element is more preferably 1 g / L or more, and still more preferably 2 g / L or more.
  • the compound or element of the fourth group element in the aqueous treatment liquid is used.
  • the content of ions is preferably 30 g / L or less.
  • the content of the compound containing a Group 4 element or the ion of a Group 4 element in the aqueous treatment liquid in terms of metal atom can be measured using a fluorescent X-ray analyzer.
  • the bond promoter can soften the fluorine resin present in the aqueous treatment liquid.
  • the fluorinated resin softened by the above-mentioned bonding promoter makes it easier for the particles constituting the emulsion to be more closely fused to each other, and forms a chemical conversion film which is more difficult to permeate water. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter does not easily generate rust, and the corrosion resistance of the chemical conversion treatment film is further enhanced.
  • the bonding promoter softens the fluorocarbon resin to make the particles constituting the emulsion adhere more closely, thereby forming a chemical conversion film that is less likely to be decomposed by light such as ultraviolet light. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter further enhances the weather resistance.
  • the said bonding promoter can fuse
  • the bonding accelerator can be appropriately selected from adipic acid or an ester compound of phthalic acid and an alcohol having 1 to 3 carbon atoms, and n-methyl-2-pyrrolidone.
  • binding promoters include dimethyl adipate, diethyl adipate, di (iso) propyl adipate, di (iso) butyl adipate, dimethyl phthalate, diethyl phthalate, di (iso) propyl phthalate, di (iso) butyl phthalate And n-methyl-2-pyrrolidone.
  • dimethyl adipate, diethyl adipate, di (iso) propyl adipate and di (iso) butyl adipate are preferable from the viewpoint of corrosion resistance and appearance of processing.
  • (iso) propyl means propyl and isopropyl
  • (iso) butyl means butyl and isobutyl.
  • the content of the bonding promoter in the aqueous treatment liquid can be, for example, 0.1 g / L or more and 50 g / L or less, but the fluorine resin can be more easily fused by the above-described action, From the viewpoint of further enhancing the corrosion resistance, it is preferably 0.5 g / L to 50 g / L, more preferably 0.7 g / L to 30 g / L, and 1 g / L to 15 g / L. It is further preferred that
  • Etchant uniforms and activates the surface of the base steel sheet to further enhance the adhesion of the chemical conversion coating and suppress the penetration of water from the chemical conversion coating to the plated steel sheet. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter does not easily generate rust, and the corrosion resistance of the chemical conversion treatment film is further enhanced.
  • the etching agent dissolves metal components such as Zn and Al contained in the plating layer and Fe contained in the base steel plate, and incorporates the dissolved metal component into the chemical conversion treatment film to form a chemical conversion treatment film. Enhance the corrosion resistance of the plated steel sheet formed.
  • the metal component taken in is taken into the inside of the emulsion-like fluorine resin by the above-mentioned bond promoter, and as a result, the adhesion of the chemical conversion treatment film is further enhanced. It is believed that the corrosion resistance of the formed plated steel sheet is further enhanced.
  • the etchant is preferably phosphoric acid or phosphate, and ammonia or ammonium salt.
  • Phosphoric acid or phosphate homogenizes and activates iron (Fe) at the exposed portion of the base steel plate or zinc (Zn) contained in Zn-based plating. Therefore, phosphoric acid or phosphate is particularly useful for steel plates and Zn-based plated steel plates.
  • the phosphoric acid or phosphate may be a water-soluble compound having a phosphate anion (PO 4 3- ).
  • phosphates include sodium phosphate, ammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, magnesium phosphate, potassium phosphate, manganese phosphate, zinc phosphate, orthophosphoric acid, metaphosphoric acid, pyrroline Acids, triphosphates, tetraphosphates and the like are included. These phosphoric acids or phosphates may be used alone or in combination of two or more.
  • ammonia acid or ammonium salt homogenizes and activates iron (Fe) at the exposed portion of the base steel plate, or aluminum (Al) contained in Al-based plating or Zn—Al-based plating. Therefore, phosphoric acid or phosphate is particularly useful for steel plates and Zn-Al-based plated steel plates.
  • ammonium salts include phosphates, fluorides and metal salts of quaternary ammonium cations (NH 4 + ) and the like. Among these, it is preferable to contain the phosphate of a quaternary ammonium cation, and it is more preferable to contain ammonium phosphate, ammonium hydrogen phosphate and ammonium dihydrogen phosphate.
  • the aqueous processing liquid is It is preferred to include both phosphoric acid or phosphate and ammonia or ammonium salt.
  • the aqueous treatment liquid comprises phosphoric acid or phosphate and ammonia or ammonium salt. It is preferable to include both of.
  • the etchant is preferably a phosphate of quaternary ammonium cation, more preferably ammonium phosphate, ammonium hydrogen phosphate and ammonium dihydrogen phosphate.
  • the content of the phosphate anion (PO 4 3- ) is preferably 1 g / L or more, and 2 g / L or more in terms of phosphate anion. More preferable.
  • the content of the etching agent in the aqueous treatment liquid the content of the quaternary ammonium cation (NH 4 + ) is preferably 1 g / L or more in terms of the quaternary ammonium cation, and 2 g / L. It is more preferable that it is more than.
  • the content of the etching agent in the aqueous processing solution is such that, when the etching agent contains both phosphoric acid or phosphate and ammonia or ammonium salt, phosphate anion (PO 4 3- ) and quaternary ammonium cation (
  • the content of NH 4 + ) is preferably 1 g / L or more, and more preferably 2 g / L or more, in terms of phosphate anion and quaternary ammonium cation, respectively.
  • silane Coupling Agent The silane coupling agent further improves the adhesion of the chemical conversion film.
  • the content of the silane coupling agent in the aqueous treatment liquid is preferably 0.5 parts by mass to 5 parts by mass with respect to 100 parts by mass of the fluorocarbon resin.
  • the adhesiveness of a chemical conversion treatment film can be improved more as content of a silane coupling agent is 0.5 mass part or more.
  • the content of the silane coupling agent is 5 parts by mass or less, a decrease in the storage stability of the aqueous treatment liquid can be suppressed.
  • the aqueous treatment liquid may contain, as other components, inorganic compounds other than those described above, organic lubricants other than silane coupling agents, inorganic lubricants, inorganic pigments, organic pigments, dyes, etc., as necessary. It is also good. Inorganic compounds (oxides, phosphates, etc.) such as Mg, Ca, Sr, V, W, Mn, B, Si, Sn etc. densify the chemical conversion film to improve water resistance. Organic lubricants such as fluorine, polyethylene, and styrene, and inorganic lubricants such as molybdenum disulfide and talc improve the lubricity of the chemical conversion film. Moreover, a predetermined
  • content of vanadium (V) ion and titanium (Ti) ion is 500 ppm or less in conversion of a metal atom in a water-based process liquid.
  • Compounds containing V or Ti may be used as a rust inhibitor, but by reducing the content of these ions, the decrease in the weatherability of the chemical conversion treatment film due to the photocatalytic action of V or Ti is suppressed be able to.
  • the content of chromium (Cr), particularly hexavalent chromium is preferably 100 ppm or less in terms of metal atom.
  • the aqueous treatment liquid preferably contains substantially no inorganic pigment, organic pigment, dye, and the like. Since the aqueous treatment liquid contains a fluorine resin as a main component, a phosphate treatment (percuralizing) to form a phosphate film with a salt of phosphoric acid such as manganese or iron, or a large amount of zinc powder forms a sacrificial anticorrosive layer Unlike zinc-rich paint, it can form clear films.
  • the aqueous treatment liquid preferably has a solid content (solid content concentration) excluding a solvent such as water of 20% by mass or more based on the total mass of the aqueous treatment liquid.
  • a solid content solid content concentration
  • a solvent such as water of 20% by mass or more
  • a chemical conversion film having a sufficient film thickness and a sufficient weather resistance can be formed.
  • the upper limit of content of solid content is 40 mass% or less from the surface of process liquid stability.
  • the aqueous treatment liquid preferably has a pH of 7.0 or more and 9.5 or less.
  • the pH is 7.0 or more
  • the etching amount of Zn can be appropriately adjusted
  • the pH is 9.5 or less
  • the etching amount of Al can be appropriately adjusted. Therefore, when the pH is 7.0 or more and 9.5 or less, the appearance defect due to excessive etching or the deterioration of the corrosion resistance can be suppressed.
  • the aqueous treatment liquid may be a one-component type, or a two-component mixture type in which an emulsion of a fluorocarbon resin and a solution (or dispersion liquid) containing a bonding accelerator are mixed at the time of use.
  • the chemical conversion treatment method of a plated steel plate The above-mentioned aqueous treatment liquid can be used for the chemical conversion treatment of a plated steel plate. Specifically, the above-mentioned aqueous treatment liquid can be applied to the end face of the plated steel sheet and dried to form a chemical conversion treatment film.
  • the type of base steel plate to be plated is not particularly limited.
  • the steel plate may be a carbon steel including low carbon steel, medium carbon steel, high carbon steel and the like, or an alloy steel containing Mn, Cr, Si, Ni and the like.
  • the steel plate may be a killed steel including Al-killed steel or the like, or may be a rimmed steel.
  • deep drawing steel sheets including low carbon Ti-added steel and low carbon Nb-added steel are preferable as steel sheets.
  • a high strength steel plate in which the amounts of P, Si, Mn, etc. are adjusted to specific values may be used.
  • the plated steel plate may be made of any of the above steel plates as a base steel plate and subjected to known plating.
  • the plating may be hot-dip plating or vapor deposition plating.
  • the type of plating is not particularly limited, and Zn-based plating (Zn plating, Zn-Al plating, Zn-Al-Mg plating, etc.), Al-based plating, Ni-based plating, etc. can be used. Among these, Zn-based plating and Al-based plating are preferable, and Zn-based plating is more preferable.
  • the aqueous treatment liquid described above can form a chemical conversion film having high adhesion to both the various plating layers and the base steel plate, so among the plated steel plates, the base steel plate such as the end face or the end face generated by cutting is exposed
  • the chemical conversion treatment film can be formed by applying to the above-described site and drying.
  • the plated steel sheet may be subjected to a base chemical conversion treatment of a precoat by a known method.
  • the application method of the aqueous treatment liquid is not particularly limited, and may be appropriately selected according to the shape of the plated steel sheet and the like.
  • Examples of the coating method include roll coating, curtain flow, spin coating, spraying, immersion pulling, and dropping.
  • the thickness of the liquid film of the aqueous treatment liquid can be adjusted by a felt throttle, an air wiper, or the like.
  • the application amount of the aqueous treatment liquid is not particularly limited, it is preferable to adjust the film thickness of the chemical conversion treatment film to be 0.5 ⁇ m or more and 10 ⁇ m or less.
  • the film thickness of the chemical conversion film is 0.5 ⁇ m or more, the chemical conversion film can be sufficiently imparted with weather resistance, corrosion resistance, color fastness and the like.
  • the film thickness is more than 10 ⁇ m, it can not be expected to improve the performance accompanying the increase of the film thickness.
  • the applied aqueous treatment liquid can be dried at normal temperature to form a chemical conversion treatment film.
  • the applied aqueous treatment liquid may be dried by heating (for example, heating to 50 ° C. or higher), but from this point of view, drying is performed from the viewpoint of suppressing the performance deterioration of the chemical conversion treatment film due to the thermal decomposition of the organic component.
  • the temperature is preferably 300 ° C. or less.
  • a chemically-treated steel sheet having a chemical conversion film formed from the above-mentioned aqueous treatment liquid comprises the above-mentioned plated steel sheet and the base steel plate of the end face of the above-mentioned plated steel sheet, preferably the end face of the above-mentioned plated steel plate And the above-described chemical conversion treatment film formed to cover the exposed portion.
  • the chemical conversion treated steel sheet may be a molded processed product.
  • the method of forming is not particularly limited, and can be selected from known methods such as pressing, punching and drawing.
  • the above-mentioned chemical conversion film comprises an organic resin containing the above-mentioned fluororesin, a compound containing the above-mentioned Group 4 element or an ion of the Group 4 element, adipic acid or phthalic acid, and one or more carbon atoms. And at least one bond promoter selected from the group consisting of an ester compound with an alcohol of 3 or less and n-methyl-2-pyrrolidone, and a silane coupling agent.
  • the content ratio of these components is the same as the ratio described above for the aqueous treatment liquid.
  • the film thickness of a chemical conversion treatment film is 0.5 micrometer or more and 10 micrometers or less.
  • the chemical conversion film can be sufficiently provided with weather resistance, corrosion resistance, discoloration resistance, and the like.
  • the film thickness is more than 10 ⁇ m, it can not be expected to improve the performance accompanying the increase of the film thickness.
  • the chemically treated steel sheet is excellent in weatherability, particularly long-term weatherability.
  • the chemically treated steel sheet having the above-mentioned chemical conversion treatment film on the end face or the like which is the exposed portion of the base steel plate produced by the forming process of the plated steel plate etc. Is preferable because it is excellent in long-term weather resistance.
  • the chemically treated steel sheet having the above-mentioned conversion treated film on the weld formed by melting and plating the plating layer has a remarkable effect of enhancing the corrosion resistance of the weld.
  • fluorine resin As the fluorine resin (FR), an aqueous emulsion of fluorine resin (Tg: -35 to 25 ° C., minimum film forming temperature (MFT): 10 ° C.) was used.
  • the solid content concentration of the fluororesin emulsion was 38% by mass, the content of fluorine atoms in the fluororesin was 25% by mass, and the average particle diameter of the emulsion was 150 nm.
  • Acrylic resin (AR) is an acrylic resin emulsion, "Patellacole” ("Patellacole” is a registered trademark of the company) manufactured by DIC Corporation.
  • the solid content concentration of "pateracol” was 40% by mass, and the average particle size of the emulsion appeared to be about 10 to 100 nm.
  • urethane resin "Hydran” manufactured by DIC Corporation, which is a urethane resin emulsion, was used.
  • the solid content concentration of "Hydran” was 35% by mass, and the average particle size of the emulsion appeared to be about 10 to 100 nm.
  • the amount of phosphoric acid is adjusted by the total amount of phosphoric acid, diammonium hydrogen phosphate and ammonium dihydrogen phosphate, and the amount of ammonium is ammonia (aqueous solution), zirconium ammonium carbonate, zirconium ammonium fluoride, phosphorus
  • the total amount of diammonium hydrogen oxide, ammonium dihydrogen phosphate and ammonium carbonate was adjusted.
  • silane coupling agent SCA
  • SilQUEST A-186 manufactured by Momentive Performance Materials Japan Ltd. was used.
  • the “F amount”, “Zr amount”, “addition amount”, “phosphoric acid amount”, “ammonium amount” and “SCA addition amount” in Table 1 are respectively the amount (% by mass) of fluorine atoms, Amount (g / L) of metal containing compound of Group 4 element or ion of Group 4 element in terms of metal atom, added amount of bonding accelerator (g / L), conversion to phosphate anion of phosphoric acid or phosphate Content (g / L), content of the ammonia or ammonium salt in terms of quaternary ammonium cation (g / L), and addition amount of the silane coupling agent (when the mass of the fluorine resin is 100% by mass) Added amount of
  • Aqueous treatment solution 1 to aqueous treatment solution 15 were stored at normal temperature for 180 days.
  • the amount of change in viscosity (the value obtained by subtracting the viscosity before storage from the viscosity after storage) before and after storage of each aqueous treatment liquid was measured using Ford Cup No. 4, and storage stability was evaluated based on the following criteria.
  • a The change in viscosity was less than 10 seconds.
  • the change in viscosity was 10 seconds or more, but there was no problem in use.
  • the change in viscosity was 30 seconds or more. Coating was difficult due to thickening.
  • Hot-dip Zn-6.0 mass% Al-3.0 mass% Mg plating layer (coating adhesion amount 90 g / m 2 ) was formed on the surface of ordinary steel with a thickness of 0.6 mm to make a plated steel sheet .
  • this plated steel sheet is cut into a width of 50 mm and a length of 100 mm, about 20% of the surface of the end face generated by cutting is covered with the plating layer, and the remaining about 80% of the surface is exposed to the base steel Was.
  • the test piece is exposed to the atmosphere for 2 years, and after 1 and 2 years, the area ratio of red rust generated on the end face of the test piece is measured, and the red rust generation area rate WR (red rust is generated
  • the end surface corrosion resistance was evaluated based on the following criteria.
  • a Red rusting area ratio WR was less than 10%
  • B Red rusting area ratio WR was more than 10% and 30% or less
  • D Red rusting area ratio WR was 50 It was over%
  • Table 2 shows the evaluation results of storage stability and corrosion resistance of the end face portion of the aqueous treatment liquid 1 to the aqueous treatment liquid 15.
  • the aqueous treatment liquid 1 to aqueous treatment liquid 10 containing an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, and a bonding accelerator The storage stability and the corrosion resistance of the formed chemical conversion film were all good.
  • the corrosion resistance is further enhanced.
  • the adhesion is low.
  • the chemical conversion film produced by the aqueous treatment liquid of the present invention can further enhance the corrosion resistance at the end face of the plated steel plate where the base steel plate is exposed by the forming process and the like.
  • the aqueous treatment liquid of the present invention is 1) steel pipes for steel or agricultural houses, shaped steels, columns, beams, conveying members, 2) sound insulation walls, sound insulation walls, sound absorption walls, snow protection walls, guard rails, balustrades, protection Rails, columns, 3) Rail vehicle members, wire members, members for electrical equipment, members for safety environment, members for construction, structural members, formation of a chemical conversion film by post coating on plated steel plates used for applications such as solar mounts Can be suitably used.

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Abstract

The objective of the present invention is to provide an anti-rust treatment solution capable of forming a chemical conversion treated film having higher corrosion resistance. The objective is achieved by an anti-rust treatment solution for an end face of a plated steel sheet, the anti-rust treatment solution including: an organic resin containing a fluorine resin; a Group 4 element-containing compound or ions of the Group 4 element; at least one bonding promoter selected from the group consisting of an n-methyl-2-pyrrolidone and an ester compound of an adipic acid or phthalic acid and a C1-C3 alcohol; and a silane coupling agent.

Description

めっき鋼板の端面防錆処理液、めっき鋼板の端面の化成処理方法、化成処理鋼板および成形加工品End surface rustproofing treatment solution for plated steel plate, method of chemical conversion treatment of end surface of plated steel plate, chemical conversion treated steel plate and molded processed product
 本発明は、めっき鋼板の端面防錆処理液、めっき鋼板の化成処理方法、化成処理鋼板および成形加工品に関する。 The present invention relates to an end face rustproofing solution for a plated steel plate, a method for forming a plated steel plate, a conversion-treated steel plate, and a shaped and processed product.
 従来、外装建材などの様々な用途において、鋼板や、鋼板の表面にZn系めっき処理などを施しためっき鋼板が使用されている。これらのめっき鋼板は、そのままでは耐食性や耐変色性などが不十分な場合があるため、有機樹脂を含む化成処理皮膜をその表面に形成されることがある。 BACKGROUND ART Conventionally, in various applications such as exterior building materials, a steel plate or a plated steel plate in which a surface of the steel plate is subjected to a Zn-based plating treatment or the like has been used. These plated steel sheets may be insufficient in corrosion resistance and color fastness as they are, and therefore, a chemical conversion coating containing an organic resin may be formed on the surface thereof.
 また、上記めっき鋼板は、成形加工品として使用されることも多い。めっき鋼板を成形加工するとき、成形により生じた端面や成形加工で生じた基材鋼板の露出部位などの耐食性などを高めるため、成形加工などの後に、端面または露出部位に化成処理皮膜を形成することがある。 Moreover, the said plated steel plate is used in many cases as a shaping | molding process goods. When forming a plated steel sheet, in order to enhance the corrosion resistance of the end face generated by forming or the exposed part of the base steel plate generated by forming, etc., after forming processing, a chemical conversion treatment film is formed on the end face or exposed part Sometimes.
 端面への化成処理皮膜の形成に用いる処理液として、特許文献1には、皮膜に耐食性を付与するCa、Mg、MnおよびZnから選ばれる金属成分、ならびに皮膜を形成するリン酸イオンおよびエチレンオキサイド基を有する有機化合物を含む処理液が記載されている。特許文献1によれば、上記処理液は、有機化合物のエチレンオキサイド基がリン酸イオンと結合してリン酸エステルによる皮膜が生成し、この皮膜中に上記金属成分が酸化物または水酸化物となって分散するとされている。 Patent Document 1 discloses, as a treatment liquid used for forming a chemical conversion film on an end face, a metal component selected from Ca, Mg, Mn and Zn which imparts corrosion resistance to the film, and phosphate ions and ethylene oxide which form the film. A treatment liquid containing an organic compound having a group is described. According to Patent Document 1, in the treatment liquid, the ethylene oxide group of the organic compound is bonded to a phosphate ion to form a film of phosphoric acid ester, and the metal component in the film is an oxide or a hydroxide. It is supposed to be dispersed.
 端面への化成処理皮膜の形成に用いる別の処理液として、特許文献2には、防錆剤としてのリン酸二水素マグネシウム、リン酸水素マグネシウムまたはL-アスコルビン酸と、端面から水を遮断するためのバインダー成分としてのシリカ微粒子と、を含む処理液が記載されている。 As another treatment liquid used for formation of a chemical conversion treatment film on the end face, Patent Document 2 blocks water from the end face with magnesium dihydrogen phosphate, magnesium hydrogen phosphate or L-ascorbic acid as a rust inhibitor. A processing solution containing silica fine particles as a binder component for the purpose is described.
 端面への化成処理皮膜の形成に用いるさらに別の処理液として、特許文献3には、腐食抑制材として不飽和アルコール類、飽和直鎖第一アミン類、飽和直鎖第二アミン類、飽和直鎖第三アミン類、チオ尿素類、ホスホン酸類、モルホリン類およびイミダゾリン類から選ばれる有機系腐食抑制剤を溶解させた水溶液が記載されている。 As another treatment liquid used for forming a chemical conversion treatment film on the end face, Patent Document 3 discloses, as a corrosion inhibitor, unsaturated alcohols, saturated linear primary amines, saturated linear secondary amines, saturated straight chain An aqueous solution in which an organic corrosion inhibitor selected from chain tertiary amines, thioureas, phosphonic acids, morpholines and imidazolines is described.
 端面への化成処理皮膜の形成に用いるさらに別の処理液として、特許文献4には、アクリル酸またはメタクリル酸のエステル類を主体とし、スチレンおよび酢酸ビニルなどのビニル系モノマーを反応させて得られる共重合体樹脂などをこれに配合したアクリルラッカーが記載されている。特許文献4によれば、当該アクリルラッカーを乾燥時の膜厚が5~30μmとなるように塗布して皮膜を形成することで、端面が均一に被覆されて防錆作用が十分に奏されるとされている。 Patent Document 4 is obtained by reacting esters of acrylic acid or methacrylic acid with a vinyl-based monomer such as styrene and vinyl acetate as another treatment liquid used for forming a chemical conversion treatment film on the end face. An acrylic lacquer is described in which a copolymer resin or the like is incorporated therein. According to Patent Document 4, the acrylic lacquer is applied so as to have a dry film thickness of 5 to 30 μm to form a film, whereby the end face is uniformly coated and a sufficient antirust action is exhibited. It is assumed.
 端面への化成処理皮膜の形成に用いるさらに別の処理液として、特許文献5には、水性ウレタン塗料と、塗布性を高めるための亜鉛粉末と、を含む水性塗料が記載されている。 As another processing solution used for formation of a chemical conversion treatment film on an end face, Patent Document 5 describes an aqueous paint containing an aqueous urethane paint and a zinc powder for enhancing the coatability.
 端面への化成処理皮膜の形成に用いるさらに別の処理液として、特許文献6~10には、第4族金属を含む化合物によってフッ素樹脂を架橋させて、フッ素樹脂を含む有機樹脂皮膜の耐水性を高めることができる、化成処理液が記載されている。 As another processing solution used for formation of a chemical conversion treatment film on the end face, Patent Documents 6 to 10 disclose water resistance of organic resin film containing fluorine resin by crosslinking fluorine resin with a compound containing Group 4 metal. The chemical conversion solution is described, which can enhance the
特開2005-248310号公報JP 2005-248310 A 特開2010-053404号公報JP, 2010-053404, A 特開2003-3280号公報JP 2003-3280 A 特開平7-224391号公報Unexamined-Japanese-Patent No. 7-224391 特開2013-010845号公報JP, 2013-010845, A 国際公開第2011/158513号WO 2011/158513 国際公開第2011/158516号WO 2011/158516 特開2012-21207号公報Unexamined-Japanese-Patent No. 2012-21207 特開2012-177146号公報JP 2012-177146 A 特開2012-177147号公報JP 2012-177147 A
 特許文献1~特許文献3に記載の処理液には、赤錆の発生を抑制する作用(防錆作用)がさほど高くなく、長期にわたって防錆効果が維持できないという問題がある。 The treatment solutions described in Patent Documents 1 to 3 have a problem that the action of suppressing the occurrence of red rust (antirust action) is not so high, and the antirust effect can not be maintained for a long time.
 また、特許文献4に記載のようにアクリルラッカーを用いた場合、膜厚が5μm以上である厚い皮膜の形成が必要となる。さらに、当該アクリルラッカーは有機溶剤を含むため、揮発した溶剤の回収工程が必要となる。これらの要因により、特許文献4に記載のアクリルラッカーを用いた防錆処理は高価になりやすい。また、アクリルラッカーから形成されるアクリル皮膜は、耐候性がさほど高くない。 Moreover, when an acrylic lacquer is used like patent document 4, formation of the thick film which is 5 micrometers or more in film thickness is needed. Furthermore, since the acrylic lacquer contains an organic solvent, a recovery step of the volatilized solvent is required. Due to these factors, the anticorrosion treatment using the acrylic lacquer described in Patent Document 4 tends to be expensive. Also, acrylic coatings formed from acrylic lacquers do not have very high weatherability.
 また、特許文献5に記載の水性ウレタン樹脂を用いた場合、塗布性を高めるために亜鉛粉末を含む処理液を用いるため、処理液が端部以外に付着したときに付着部位が亜鉛粉末によって着色され、外観が損なわれかねない。 Moreover, when using the aqueous | water-based urethane resin of patent document 5, since a process liquid containing zinc powder is used in order to improve coating property, when a process liquid adheres other than an edge part, an adhesion part is colored by zinc powder. And the appearance may be impaired.
 これに対し、特許文献6~10に記載のように、フッ素樹脂および第4族金属を含む化成処理液を用いて化成処理皮膜を形成すると、透明でありかつ耐候性に優れた皮膜を形成できるうえ、フッ素樹脂の架橋により化成処理皮膜の耐水性を高めることもできるため非常に有用である。 On the other hand, as described in Patent Documents 6 to 10, when a chemical conversion treatment film is formed using a chemical conversion solution containing a fluorine resin and a Group 4 metal, a transparent film having excellent weather resistance can be formed. In addition, since the water resistance of the chemical conversion film can be enhanced by crosslinking of the fluorine resin, it is very useful.
 しかし、上記めっき鋼板の成形加工品は、屋外の様々な環境で使用されるため、化成処理皮膜の耐候性を高めるのみならず、赤錆の発生をより抑制する(耐食性をより高める)ことに対する要望は依然として存在する。 However, since the molded and processed product of the above-described plated steel sheet is used in various environments outdoors, it is desired not only to improve the weatherability of the chemical conversion film but also to further suppress the occurrence of red rust (to improve the corrosion resistance) Still exist.
 上記の課題に鑑み、本発明は、耐食性がより高められた化成処理皮膜を形成可能な端面防錆処理液、上記端面防錆処理液を用いる化成処理方法、ならびに上記化成処理方法で形成される化成処理皮膜を有する化成処理鋼板および成形加工品を提供することを、その目的とする。 In view of the above problems, the present invention is formed by an end face rustproofing treatment liquid capable of forming a chemical conversion treated film with higher corrosion resistance, a chemical conversion treatment method using the endface rustproofing treatment liquid, and the chemical conversion treating method An object of the present invention is to provide a chemically treated steel sheet having a chemical conversion film and a shaped and processed product.
 上記の課題に鑑み、本発明の一態様は、めっき鋼板の化成処理用の端面防錆処理液に関する。上記端面防錆処理液は、フッ素樹脂を含む有機樹脂と、第4族元素を含む化合物または第4族元素のイオンと、エッチング剤と、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、シランカップリング剤と、を含む。 In view of the above problems, one aspect of the present invention relates to an end face rustproofing solution for chemical conversion treatment of a plated steel plate. The above-mentioned end face rustproofing treatment liquid is an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms. And one or more bonding promoters selected from the group consisting of n-methyl-2-pyrrolidone and a silane coupling agent.
 また、本発明の他の態様は、めっき鋼板の化成処理方法に関する。上記化成処理方法は、めっき鋼板の端面に、めっき鋼板の化成処理用の端面防錆処理液を付与する工程を含む。上記端面防錆処理液は、フッ素樹脂を含む有機樹脂と、第4族元素を含む化合物または第4族元素のイオンと、エッチング剤と、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、を含む。 Moreover, the other aspect of this invention is related with the chemical conversion treatment method of a plated steel plate. The chemical conversion treatment method includes the step of applying an end surface rustproofing solution for chemical conversion treatment of the plated steel sheet to the end surface of the plated steel sheet. The above-mentioned end face rustproofing treatment liquid is an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms. And one or more bonding promoters selected from the group consisting of n-methyl-2-pyrrolidone.
 また、本発明のさらに他の態様は、めっき鋼板と、前記めっき鋼板の端面に形成された化成処理皮膜と、を有する化成処理鋼板に関する。上記化成処理皮膜は、フッ素樹脂を含む有機樹脂と、第4族元素を含む化合物または第4族元素のイオンと、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、シランカップリング剤と、を含む。 Moreover, the further another aspect of this invention is related with the chemical conversion treatment steel plate which has a plated steel plate and the chemical conversion treatment film formed in the end surface of the said plated steel plate. The chemical conversion film is an ester compound of an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms, and at least one bond promoter selected from the group consisting of n-methyl-2-pyrrolidone and a silane coupling agent.
 また、本発明のさらに他の態様は、めっき鋼板の成形加工によって作製された成形加工品に関する。上記成形加工品は、前記めっき鋼板の端面に形成された化成処理皮膜を含み、上記化成処理皮膜は、フッ素樹脂を含む有機樹脂と、第4族元素を含む化合物または第4族元素のイオンと、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、シランカップリング剤と、を含む。 Moreover, the further another aspect of this invention relates to the shaping | molding processed article produced by the shaping | molding process of the plated steel plate. The molded product includes a chemical conversion film formed on an end face of the plated steel sheet, and the chemical conversion film includes an organic resin containing a fluorine resin, a compound containing a Group 4 element, or an ion of a Group 4 element. And one or more bond promoters selected from the group consisting of adipic acid or an ester compound of phthalic acid and an alcohol having 1 to 3 carbon atoms, and n-methyl-2-pyrrolidone, and a silane coupling agent Including.
 本発明によれば、耐食性がより高められた化成処理皮膜を形成可能な端面防錆処理液、上記端面防錆処理液を用いる化成処理方法、ならびに上記化成処理方法で形成される化成処理皮膜を有する化成処理鋼板および成形加工品が提供される。 According to the present invention, an end face rustproofing treatment liquid capable of forming a chemical conversion treatment film having higher corrosion resistance, a chemical conversion treatment method using the endface rustproofing treatment liquid, and a chemical conversion treated film formed by the chemical conversion treatment method The chemical conversion treatment steel plate which has it, and a shaping | molding processed article are provided.
 本発明者らは、鋭意検討の結果、フッ素樹脂を含む有機樹脂および第4族元素を含む化合物または第4族元素のイオンを含む水系処理液に、特定の化合物(以下、単に「結合促進剤」ともいう。)と、シランカップリング剤と、をさらに含有させて、端面防錆処理液とすることで、めっき鋼板の端面に形成される化成処理皮膜の耐食性がより高まることを見出した。本発明者らは、この耐食性の向上をもたらす作用効果についてさらに検討した結果、上記結合促進剤としてアジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンが使用できることを見出し、もって本発明を完成させた。 The inventors of the present invention, as a result of intensive studies, have identified specific compounds (hereinafter simply referred to as “bond promoters” in an aqueous resin containing an organic resin containing a fluorine resin and a compound containing a Group 4 element or an ion of a Group 4 element. Furthermore, it was found that the corrosion resistance of the chemical conversion film formed on the end face of the plated steel plate is further enhanced by further containing a silane coupling agent to obtain an end face rustproofing solution. The inventors of the present invention have further studied the action and effect of improving the corrosion resistance, and as a result, an ester compound of adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms as the bond promoter, and n-methyl-2 It has been found that pyrrolidone can be used, thus completing the present invention.
 つまり、上記結合促進剤は、通常はエマルションとして水系処理液中に存在するフッ素樹脂を、軟質化することができる。上記結合促進剤によって軟質化したフッ素樹脂は、より融着しやすくなり、耐水性がより高い化成処理皮膜を形成するため、化成処理皮膜の耐候性がより高まると考えられる。 That is, the above-mentioned bond promoter can soften the fluorocarbon resin which is usually present in the aqueous treatment liquid as an emulsion. The fluororesin softened by the bonding promoter is more likely to be fused and forms a chemical conversion treated film having higher water resistance, so that it is considered that the weather resistance of the chemical conversion treated film is further enhanced.
 1.水系処理液
 上記水系処理液は、フッ素樹脂を含む有機樹脂、第4族元素を含む化合物または第4族元素のイオン、および上記結合促進剤を含む。上記水系処理液は、エッチング剤などのその他の成分をさらに含んでもよい。
1. Aqueous Treatment Liquid The aqueous treatment liquid contains an organic resin containing a fluorocarbon resin, a compound containing a Group 4 element or an ion of a Group 4 element, and the bond promoter. The aqueous processing solution may further contain other components such as an etching agent.
 1-1.有機樹脂
 有機樹脂は、フッ素樹脂を含む有機樹脂である。フッ素樹脂は、化成処理皮膜の耐候性(耐紫外線性および耐光性など)および耐食性(赤錆の防止など)を高めることができる。なお、有機樹脂は、化成処理皮膜の耐候性および耐食性を顕著に低下させない限りにおいて、フッ素樹脂以外の樹脂を含んでもよい。
1-1. Organic resin The organic resin is an organic resin containing a fluorocarbon resin. The fluorine resin can enhance the weather resistance (such as ultraviolet light resistance and light resistance) and corrosion resistance (such as prevention of rust) of the chemical conversion film. The organic resin may contain a resin other than the fluorocarbon resin as long as the weatherability and corrosion resistance of the chemical conversion film are not significantly reduced.
 フッ素樹脂は、溶剤系フッ素樹脂と水系フッ素樹脂に大別される。これらのうち、揮発した溶剤の回収が問題とならない水系処理液に用いることが容易な、水系フッ素樹脂を用いることが好ましい。 Fluororesins are roughly classified into solvent-based fluorocarbon resins and aqueous fluorocarbon resins. Among these, it is preferable to use a water-based fluorine resin which is easy to use for a water-based treatment liquid in which recovery of the volatilized solvent is not a problem.
 水系フッ素樹脂とは、親水性官能基を有するフッ素樹脂を意味する。親水性官能基の好ましい例には、カルボキシル基およびスルホン酸基、ならびにこれらの塩などが含まれる。カルボキシル基またはスルホン酸基の塩の例には、アンモニウム塩、アミン塩、およびアルカリ金属塩などが含まれる。 The water-based fluorine resin means a fluorine resin having a hydrophilic functional group. Preferred examples of hydrophilic functional groups include carboxyl and sulfonic acid groups, salts thereof and the like. Examples of salts of carboxyl groups or sulfonic acid groups include ammonium salts, amine salts, alkali metal salts and the like.
 水系フッ素樹脂は、親水性官能基の量が0.05質量%以上5質量%以下の量であることが好ましい。親水性官能基の量が0.05質量%以上5質量%以下の量であるフッ素樹脂は、乳化剤をほとんど使用せずとも、水系エマルションとすることができる。乳化剤をほとんど含まない化成処理皮膜は、耐水性に優れた化成処理皮膜とすることができる。 The water-based fluorine resin preferably has an amount of hydrophilic functional groups of 0.05% by mass to 5% by mass. The fluorine resin in which the amount of the hydrophilic functional group is 0.05% by mass or more and 5% by mass or less can be made into an aqueous emulsion without using any emulsifying agent. The chemical conversion film containing substantially no emulsifier can be a chemical conversion film excellent in water resistance.
 水系フッ素樹脂中の親水性官能基の含有量は、水系フッ素樹脂に含まれる親水性官能基の総モル質量を、水系フッ素樹脂の数平均分子量で除して求めればよい。カルボキシル基のモル質量は45であり、スルホン酸基のモル質量は81であるので、水系フッ素樹脂に含まれるカルボキシル基およびスルホン酸基それぞれの数を求め、それぞれにモル質量を乗じることで、水系フッ素樹脂に含まれる親水性官能基の総モル質量が求まる。水系フッ素樹脂の数平均分子量はGPCで測定され得る。 The content of the hydrophilic functional group in the water-based fluorine resin may be determined by dividing the total molar mass of the hydrophilic functional group contained in the water-based fluorine resin by the number average molecular weight of the water-based fluorine resin. The molar mass of the carboxyl group is 45, and the molar mass of the sulfonic acid group is 81. Therefore, the number of each of the carboxyl group and the sulfonic acid group contained in the aqueous fluorocarbon resin is determined, and each is multiplied by the molar mass to obtain an aqueous system. The total molar mass of hydrophilic functional groups contained in the fluorocarbon resin is determined. The number average molecular weight of the aqueous fluororesin can be measured by GPC.
 水系フッ素樹脂におけるカルボキシル基は、鋼板またはめっき層(または下地化成処理皮膜)の表面と水素結合などを形成して、化成処理皮膜と鋼板またはめっき層(または下地化成処理皮膜)表面との密着性の向上に寄与するが、Hが解離しにくいため第4族元素を含む化合物または第4族元素のイオンとの架橋反応が生じにくい。一方、水系フッ素樹脂におけるスルホン酸基は、Hが解離しやすいため第4族元素を含む化合物または第4族元素のイオンとの架橋反応が生じやすいものの、一方で第4族元素を含む化合物または第4族元素のイオンと架橋反応せずに未反応のまま皮膜中に残存すると、水分子の吸着作用が強いため化成処理皮膜の耐水性を著しく低下させてしまうおそれがある。したがって、それぞれの特徴を活かすべく、水系フッ素樹脂には、カルボキシル基およびスルホン酸基の両方を含むことが好ましい。この場合、カルボキシル基とスルホン酸基との比率は、カルボキシル基/スルホン酸基のモル比で5以上60以下の範囲内が好ましい。 The carboxyl group in the water-based fluorine resin forms a hydrogen bond or the like with the surface of the steel plate or plating layer (or base chemical conversion treatment film), and the adhesion between the chemical conversion treatment film and the steel plate or plating layer (or base chemical conversion treatment film) surface However, since H + is difficult to dissociate, a cross-linking reaction with a compound containing a Group 4 element or an ion of a Group 4 element hardly occurs. On the other hand, the sulfonic acid group in the aqueous fluorocarbon resin is likely to cause a cross-linking reaction with a compound containing a Group 4 element or an ion of a Group 4 element because H + is easily dissociated, but a compound containing a Group 4 element Alternatively, if it remains unreacted in the film without undergoing a crosslinking reaction with ions of a Group 4 element, the water molecule adsorption is strong, which may significantly reduce the water resistance of the chemical conversion film. Therefore, in order to take advantage of the respective features, it is preferable that the aqueous fluororesin contain both a carboxyl group and a sulfonic acid group. In this case, the ratio of carboxyl group to sulfonic acid group is preferably in the range of 5 or more and 60 or less in terms of the molar ratio of carboxyl group / sulfonic acid group.
 水系フッ素樹脂の数平均分子量は、1000以上が好ましく、1万以上がより好ましく、20万以上が特に好ましい。 The number average molecular weight of the aqueous fluororesin is preferably 1,000 or more, more preferably 10,000 or more, and particularly preferably 200,000 or more.
 水系フッ素樹脂の数平均分子量の下限が上記値であると、化成処理皮膜の透水性および耐水性を十分に高めることができ、湿気や腐食性ガスなどが化成処理皮膜を貫通することによるめっき鋼板の腐食を抑制することができる。また、水系フッ素樹脂の数平均分子量の下限が上記値であると、光エネルギーなどの作用により発生したラジカルがポリマー鎖の末端に作用しにくいため、水などの相乗作用により水系フッ素樹脂が加水分解されてしまうことによる、化成処理皮膜の劣化を抑制することもできる。水系フッ素樹脂の分子量を大きくすることにより、分子間力が強くなり、化成処理皮膜の凝集力が高まるため、化成処理皮膜の耐水性をより高めることができる。また、水系フッ素樹脂の分子量を大きくすることにより、水系フッ素樹脂の主鎖における原子間の結合を安定化して、水系フッ素樹脂の加水分解による化成処理皮膜の劣化も生じにくくなる。 The water permeability and water resistance of a chemical conversion treatment film can fully be improved as the lower limit of the number average molecular weight of water-based fluorine resin is the above value, and a plated steel sheet by moisture, corrosive gas, etc. penetrating a chemical conversion treatment film Corrosion can be suppressed. In addition, when the lower limit of the number average molecular weight of the water-based fluorine resin is the above value, radicals generated by the action of light energy and the like are less likely to act on the end of the polymer chain. It is also possible to suppress the deterioration of the chemical conversion coating due to being done. By increasing the molecular weight of the water-based fluorine resin, the intermolecular force becomes strong, and the cohesion of the chemical conversion treatment film is enhanced, whereby the water resistance of the chemical conversion treatment film can be further enhanced. In addition, by increasing the molecular weight of the water-based fluorine resin, the bond between atoms in the main chain of the water-based fluorine resin is stabilized, and the deterioration of the chemical conversion treatment film due to the hydrolysis of the water-based fluorine resin also hardly occurs.
 一方で、水系フッ素樹脂の数平均分子量は、200万以下が好ましい。水系フッ素樹脂の数平均分子量の上限が200万以下であれば、水系処理液のゲル化などが生じにくく、水系処理液の保存安定性がより高まる。 On the other hand, the number average molecular weight of the aqueous fluororesin is preferably 2,000,000 or less. When the upper limit of the number average molecular weight of the water-based fluororesin is 2,000,000 or less, gelation of the water-based treatment liquid is unlikely to occur, and the storage stability of the water-based treatment liquid is further enhanced.
 水系フッ素樹脂は、化成処理皮膜の耐候性および耐食性をより高める観点から、上記フッ素樹脂の全質量に対して6質量%以上のフッ素(F)原子を含むことが好ましく、8質量%以上のフッ素(F)原子を含むことがより好ましく、13質量%以上のフッ素(F)原子を含むことがさらに好ましい。また、水系フッ素樹脂は、塗料化を容易にし、かつ、化成処理皮膜の密着性および乾燥性をより高める観点から、前記フッ素樹脂の全質量に対して20質量%以下のフッ素(F)原子を含むことが好ましい。水系フッ素樹脂中のフッ素(F)原子の含有量は、蛍光X線分析装置を用いることで測定することができる。 The water-based fluorine resin preferably contains 6 mass% or more of fluorine (F) atoms with respect to the total mass of the fluorine resin, from the viewpoint of further improving the weather resistance and corrosion resistance of the chemical conversion film, 8 mass% or more It is more preferable to include the (F) atom, and it is further preferable to include the fluorine (F) atom of 13% by mass or more. Further, from the viewpoint of facilitating the formation of a coating and improving the adhesion and drying properties of the chemical conversion film, the water-based fluorine resin has a fluorine (F) atom of 20% by mass or less based on the total mass of the fluorine resin. It is preferable to include. The content of fluorine (F) atoms in the water-based fluorine resin can be measured by using a fluorescent X-ray analyzer.
 水系フッ素樹脂としては、フッ素含有オレフィン樹脂であることが好ましい。フッ素含有オレフィン樹脂の例には、フルオロオレフィンと親水性官能基含有モノマーとの共重合体が含まれる。 The water-based fluorine resin is preferably a fluorine-containing olefin resin. Examples of fluorine-containing olefin resins include copolymers of fluoroolefins and hydrophilic functional group-containing monomers.
 上記フルオロオレフィンの例には、テトラフルオロエチレン、トリフルオロエチレン、クロロトリフルオロエチレン、ヘキサフルオロプロピレン、フッ化ビニル、フッ化ビニリデン、ペンタフルオロプロピレン、2,2,3,3-テトラフルオロプロピレン、3,3,3-トリフルオロプロピレン、ブロモトリフルオロエチレン、1-クロロ-1,2-ジフルオロエチレン、および1,1-ジクロロ-2,2-ジフルオロエチレンなどが含まれる。これらのフルオロオレフィンは、単独で使用されてもよいし、2種類以上を組み合わせて使用されてもよい。耐紫外線性をより高める観点からは、これらのフルオロオレフィンの中でも、テトラフルオロエチレンおよびヘキサフルオロプロピレンなどを含むパーフルオロオレフィン、ならびにフッ化ビニリデンなどが好ましい。なお、塩素イオンによる腐食を抑制する観点からは、クロロトリフルオロエチレンなどの塩素を含むフルオロオレフィンの含有量は少ない(たとえば0.1モル%以下)ことが好ましい。 Examples of the above fluoroolefins include tetrafluoroethylene, trifluoroethylene, chlorotrifluoroethylene, hexafluoropropylene, vinyl fluoride, vinylidene fluoride, pentafluoropropylene, 2,2,3,3-tetrafluoropropylene, 3 And 3,3,3-trifluoropropylene, bromotrifluoroethylene, 1-chloro-1,2-difluoroethylene, 1,1-dichloro-2,2-difluoroethylene and the like. These fluoroolefins may be used alone or in combination of two or more. Among these fluoroolefins, perfluoroolefins including tetrafluoroethylene and hexafluoropropylene, and vinylidene fluoride are preferable from the viewpoint of further enhancing the UV resistance. The content of the fluoroolefin containing chlorine such as chlorotrifluoroethylene is preferably small (for example, 0.1 mol% or less) from the viewpoint of suppressing the corrosion by the chlorine ion.
 上記親水性官能基含有モノマーの例には、公知のカルボキシル基含有モノマーおよびスルホン酸基含有モノマーが含まれる。これらの親水性官能基含有モノマーは、単独で使用されてもよいし、2種類以上を組み合わせて使用されてもよい。 Examples of the hydrophilic functional group-containing monomer include known carboxyl group-containing monomers and sulfonic acid group-containing monomers. These hydrophilic functional group-containing monomers may be used alone or in combination of two or more.
 上記カルボキシル基含有モノマーの一例としては、以下の式(1)に示される不飽和カルボン酸、およびこれらのエステルまたは酸無水物などを含む不飽和カルボン酸類が挙げられる。 Examples of the carboxyl group-containing monomer include unsaturated carboxylic acids represented by the following formula (1), and unsaturated carboxylic acids including their esters or acid anhydrides.
Figure JPOXMLDOC01-appb-C000001
 (式中、R、RおよびRは、独立に、水素原子、アルキル基、カルボキシル基またはエステル基を示す。nは0~20の整数である。)
Figure JPOXMLDOC01-appb-C000001
(Wherein, R 1 , R 2 and R 3 independently represent a hydrogen atom, an alkyl group, a carboxyl group or an ester group. N is an integer of 0 to 20.)
 上記式(1)に示される不飽和カルボン酸の具体例には、アクリル酸、メタクリル酸、ビニル酢酸、クロトン酸、桂皮酸、イタコン酸、イタコン酸モノエステル、マレイン酸、マレイン酸モノエステル、フマル酸、フマル酸モノエステル、5-ヘキセン酸、5-ヘプテン酸、6-ヘプテン酸、7-オクテン酸、8-ノネン酸、9-デセン酸、10-ウンデシレン酸、11-ドデシレン酸、17-オクタデシレン酸、およびオレイン酸などが含まれる。 Specific examples of the unsaturated carboxylic acid represented by the above formula (1) include acrylic acid, methacrylic acid, vinylacetic acid, crotonic acid, cinnamic acid, itaconic acid, itaconic acid monoester, maleic acid, maleic acid monoester, fumar Acid, fumaric acid monoester, 5-hexenoic acid, 5-heptenoic acid, 6-heptenoic acid, 7-octenoic acid, 8-nonenoic acid, 9-decenoic acid, 10-undecylenic acid, 11-dodecylenic acid, 17-octadecyrene Acids and oleic acid are included.
 上記カルボキシル基含有モノマーの別の例としては、以下の式(2)に示されるカルボキシル基含有ビニルエーテルモノマーが挙げられる。 As another example of the said carboxyl group-containing monomer, the carboxyl group-containing vinyl ether monomer shown by following formula (2) is mentioned.
Figure JPOXMLDOC01-appb-C000002
 (式中、RおよびRは、独立に、飽和または不飽和の直鎖または環状アルキル基を示す。nは0または1である。mは0または1である。)
Figure JPOXMLDOC01-appb-C000002
(Wherein, R 4 and R 5 independently represent a saturated or unsaturated linear or cyclic alkyl group, n is 0 or 1, and m is 0 or 1.)
 上記式(2)に示されるカルボキシル基含有ビニルエーテルモノマーの具体例には、3-(2-アリロキシエトキシカルボニル)プロピオン酸、3-(2-アリロキシブトキシカルボニル)プロピオン酸、3-(2-ビニロキシエトキシカルボニル)プロピオン酸、および3-(2-ビニロキシブトキシカルボニル)プロピオン酸などが含まれる。 Specific examples of the carboxyl group-containing vinyl ether monomer represented by the above formula (2) include 3- (2-allyloxyethoxycarbonyl) propionic acid, 3- (2-allyloxybutoxycarbonyl) propionic acid, 3- (2- And vinyloxyethoxycarbonyl) propionic acid, 3- (2-vinyloxybutoxycarbonyl) propionic acid and the like.
 上記スルホン酸基含有モノマーの具体例としては、ビニルスルホン酸、アリルスルホン酸、メタリルスルホン酸、スチレンスルホン酸、2-アクリルアミド-2-メチルプロパンスルホン酸、2-メタクリロイルオキシエタンスルホン酸、3-メタクリロイルオキシプロパンスルホン酸、4-メタクリロイルオキシブタンスルホン酸、3-メタクリロイルオキシ-2-ヒドロキシプロパンスルホン酸、3-アクリロイルオキシプロパンスルホン酸、アリルオキシベンゼンスルホイン酸、メタリルオキシベンゼンスルホン酸、イソプレンスルホン酸、および3-アリロキシ-2-ヒドロキシプロパンスルホン酸などが挙げられる。 Specific examples of the sulfonic acid group-containing monomer include vinyl sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, styrene sulfonic acid, 2-acrylamido-2-methylpropane sulfonic acid, 2-methacryloyloxyethane sulfonic acid, 3- Methacryloyloxypropane sulfonic acid, 4-methacryloyloxybutane sulfonic acid, 3-methacryloyloxy-2-hydroxypropane sulfonic acid, 3-acryloyloxypropane sulfonic acid, allyloxy benzene sulfo inic acid, methalyloxy benzene sulfonic acid, isoprene sulfone And acids and 3-allyloxy-2-hydroxypropane sulfonic acid.
 上記フルオロオレフィンと親水性官能基含有モノマーとの共重合体には、必要に応じて、共重合可能な他のモノマーがさらに共重合されていてもよい。上記共重合可能な他のモノマーとしては、カルボン酸ビニルエステル類、アルキルビニルエーテル類、および非フッ素系オレフィン類などが挙げられる。 The copolymer of the fluoroolefin and the hydrophilic functional group-containing monomer may be further copolymerized with another copolymerizable monomer, if necessary. Examples of the other copolymerizable monomer include carboxylic acid vinyl esters, alkyl vinyl ethers and non-fluorinated olefins.
 上記カルボン酸ビニルエステル類は、上記水系フッ素樹脂の相溶性および化成処理皮膜の光沢を向上させたり、ガラス転移温度を上昇させたりすることができる。上記カルボン酸ビニルエステル類の例には、酢酸ビニル、プロピオン酸ビニル、酪酸ビニル、イソ酪酸ビニル、ピバリン酸ビニル、カプロン酸ビニル、バーサチック酸ビニル、ラウリン酸ビニル、ステアリン酸ビニル、シクロヘキシルカルボン酸ビニル、安息香酸ビニル、およびパラ-t-ブチル安息香酸ビニルなどが含まれる。 The carboxylic acid vinyl esters can improve the compatibility of the water-based fluorine resin and the gloss of the chemical conversion film, and can increase the glass transition temperature. Examples of the above-mentioned vinyl carboxylates include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl isobutyrate, vinyl pivalate, vinyl caproate, vinyl versatate, vinyl laurate, vinyl stearate, vinyl cyclohexylcarboxylate, Vinyl benzoate and vinyl para-t-butyl benzoate and the like are included.
 上記アルキルビニルエーテル類は、化成処理皮膜の光沢および柔軟性を向上させることができる。上記アルキルビニルエーテル類の例には、メチルビニルエーテル、エチルビニルエーテル、およびブチルビニルエーテルなどが含まれる。 The alkyl vinyl ethers can improve the gloss and the flexibility of the chemical conversion film. Examples of the above alkyl vinyl ethers include methyl vinyl ether, ethyl vinyl ether, butyl vinyl ether and the like.
 上記非フッ素系オレフィン類は、化成処理皮膜の可撓性を向上させることができる。上記非フッ素系オレフィン類の例には、エチレン、プロピレン、n-ブテン、およびイソブテンなどが含まれる。 The non-fluorinated olefins can improve the flexibility of the chemical conversion film. Examples of the non-fluorinated olefins include ethylene, propylene, n-butene, and isobutene.
 たとえば、上記モノマーを乳化重合法で共重合させることで、親水性官能基を有するフルオロオレフィン共重合体のエマルションを得ることができる。このとき、フルオロオレフィン共重合体が0.05質量%以上5質量%以下の量の親水性官能基を有するように、原料モノマー組成物におけるフルオロオレフィンの量を調整することで、乳化剤をほとんど使用せずにフルオロオレフィン共重合体の水系エマルションを製造することができる。乳化剤をほとんど含有しない(1質量%以下)フルオロオレフィン共重合体のエマルションを用いて形成された化成処理皮膜は、乳化剤がほとんど含まれないため、乳化剤の残留による耐水性の劣化がほとんど見られず、優れた耐水性を発揮する。 For example, an emulsion of a fluoroolefin copolymer having a hydrophilic functional group can be obtained by copolymerizing the above-described monomers by an emulsion polymerization method. At this time, most of the emulsifier is used by adjusting the amount of fluoroolefin in the raw material monomer composition such that the fluoroolefin copolymer has a hydrophilic functional group in an amount of 0.05% by mass to 5% by mass. An aqueous emulsion of a fluoroolefin copolymer can be produced without. A chemical conversion film formed using an emulsion of a fluoroolefin copolymer containing hardly any emulsifier (less than 1% by mass) hardly contains any emulsifier, and therefore almost no deterioration in water resistance due to the residual emulsifier is observed Demonstrates excellent water resistance.
 上述のような方法で作製したフッ素樹脂は、水系処理液中でも粒子状で存在すると考えられる。フッ素樹脂のエマルションの平均粒径は、50nm以上300nm以下であることが好ましい。エマルションの平均粒径を50nm以上とすることで、水系処理液の保存安定性を高めることができる。また、エマルションの平均粒径を300nm以下とすることで、エマルションの表面積を増やして互いに融着しやすくさせ、低温(例えば55℃)で焼き付けたときの造膜をより容易にできる。たとえば、乳化重合法でエマルションを調製する際に、せん断速度や攪拌時間を最適化することで、エマルションの平均粒径を上記範囲内とすることができる。 The fluorine resin produced by the method as described above is considered to exist in the form of particles in the aqueous treatment liquid. The average particle size of the fluororesin emulsion is preferably 50 nm or more and 300 nm or less. The storage stability of the aqueous treatment liquid can be enhanced by setting the average particle size of the emulsion to 50 nm or more. In addition, by setting the average particle diameter of the emulsion to 300 nm or less, the surface area of the emulsion is increased to easily fuse them together, and film formation when baked at a low temperature (for example, 55 ° C.) can be made easier. For example, when preparing an emulsion by an emulsion polymerization method, the average particle diameter of the emulsion can be brought into the above range by optimizing the shear rate and the stirring time.
 水系処理液中のフッ素樹脂の含有量は、水100質量部に対して、10質量部以上70質量部以下であることが好ましい。フッ素樹脂の含有量が10質量部以上であると、乾燥過程において多量の水の蒸発することによる、化成処理皮膜の成膜性および緻密性の低下がより生じにくい。一方、フッ素樹脂の含有量が70質量部以下であると、水系処理液の保存安定性がより高まる。 The content of the fluorine resin in the aqueous treatment liquid is preferably 10 parts by mass or more and 70 parts by mass or less with respect to 100 parts by mass of water. When the content of the fluorine resin is 10 parts by mass or more, the film formability and the compactness of the chemical conversion film are less likely to be lowered by evaporation of a large amount of water in the drying process. On the other hand, when the content of the fluorine resin is 70 parts by mass or less, the storage stability of the aqueous treatment liquid is further enhanced.
 また、水系処理液中のフッ素樹脂の含有量は、固形分(水その他の溶媒を除いた成分)の合計量に対して、70質量%以上99質量%以下であることが好ましい。 In addition, the content of the fluorine resin in the aqueous treatment liquid is preferably 70% by mass or more and 99% by mass or less with respect to the total amount of the solid content (component excluding water and other solvents).
 1-2.第4族元素を含む化合物または第4族元素のイオン
 第4族元素を含む化合物または第4族元素のイオンは、フッ素樹脂、特には水系フッ素樹脂中のカルボキシル基やスルホン酸基などの官能基と反応しやすく、水系フッ素樹脂の硬化または架橋反応を促進する。そのため、第4族元素を含む化合物または第4族元素のイオンは、フッ素樹脂の密着性を高め、かつ、低温乾燥でも化成処理皮膜の耐水性を向上させることができる。
1-2. Compound containing Group 4 element or ion of Group 4 element Compound containing group 4 element or ion of Group 4 element is a fluorine resin, in particular, a functional group such as a carboxyl group or a sulfonic acid group in a water-based fluorine resin It easily reacts with water, and promotes the curing or crosslinking reaction of the water-based fluorocarbon resin. Therefore, the compound of the Group 4 element or the ion of the Group 4 element can improve the adhesion of the fluorine resin, and improve the water resistance of the chemical conversion film even at low temperature drying.
 第4族元素を含む化合物は、4A族金属の酸素酸塩、フッ化物、水酸化物、有機酸塩、炭酸塩、過酸化塩、アンモニウム塩、アルカリ金属塩、およびアルカリ土類金属塩などとすることができる。なお、酸素酸塩は、酸素と別の元素とを有する酸(炭酸や硫酸など)との塩を意味する。酸素酸塩の例には、水素酸塩、炭酸塩、硫酸塩などが含まれる。第4族元素のイオンの例には、上記化合物に由来する、第4族元素のイオンが含まれる。 Compounds containing Group 4 elements include oxyacids, fluorides, hydroxides, organic acid salts, carbonates, peroxides, ammonium salts, alkali metal salts, and alkaline earth metal salts of Group 4A metals. can do. Note that the oxy acid salt means a salt with an acid having carbon and another element (such as carbonic acid or sulfuric acid). Examples of oxy acid salts include hydrogen salts, carbonates, sulfates and the like. Examples of ions of the Group 4 element include ions of the Group 4 element derived from the above compounds.
 上記第4族元素を含む化合物または第4族元素のイオンの例には、チタン(Ti)化合物、ジルコニウム(Zr)化合物およびハフニウム(Hf)化合物が含まれる。これらのうち、後述する光触媒による耐候性の低下を抑制する観点からは、ジルコニウム化合物が好ましい。 Examples of the compound containing a Group 4 element or the ion of a Group 4 element include titanium (Ti) compounds, zirconium (Zr) compounds and hafnium (Hf) compounds. Among these, a zirconium compound is preferable from the viewpoint of suppressing a decrease in weatherability due to a photocatalyst described later.
 第4族元素を含む化合物または第4族元素のイオンは、メラミン樹脂とは異なり、エステル結合やホルムエーテル結合などが酸化および加水分解などすることによる化成処理皮膜の耐候劣化を生じにくい。また、第4族元素を含む化合物または第4族元素のイオンは、メラミン樹脂とは異なり、酸性雨に含まれる硫酸イオンや硝酸イオンなどの酸性物質によって架橋構造が切断されることによる化成処理皮膜の耐候劣化も生じにくい。 Unlike a melamine resin, a compound containing a Group 4 element or an ion of a Group 4 element is less likely to cause weathering deterioration of a chemical conversion treatment film due to oxidation or hydrolysis of an ester bond or a formal ether bond. In addition, unlike the melamine resin, the compound containing a Group 4 element or the ion of a Group 4 element is a chemical conversion treated film in which the cross-linked structure is cut by an acidic substance such as sulfate ion or nitrate ion contained in acid rain. It is hard to produce the weathering deterioration of.
 また、第4族元素を含む化合物または第4族元素のイオンは、イソシアネート樹脂を用いた架橋部分に形成されるウレタン結合よりも強い結合力でフッ素樹脂を架橋させるため、架橋構造の切断による耐候劣化の進行もより生じにくい。 In addition, since the compound of the Group 4 element or the ion of the Group 4 element crosslinks the fluorine resin with a stronger bonding force than the urethane bond formed in the cross-linked portion using the isocyanate resin, the weathering by cutting the cross-linked structure Progress of deterioration is less likely to occur.
 また、第4族元素を含む化合物または第4族元素のイオンは、化成処理皮膜の皮膜密着性、耐水性および耐変色性も向上させる。たとえば、Al含有Zn系合金めっき鋼板の表面に第4族元素を含む化合物または第4族元素のイオンを含む水系処理液で化成処理皮膜を形成させると、めっき鋼板の表面に存在する強固なAl酸化物による皮膜密着性の低下を抑制することができる。また、Al含有Zn系合金めっき鋼板の表面に第4族元素を含む化合物または第4族元素のイオンを含む水系処理液で化成処理皮膜を形成させると、エッチング反応などにより溶出したAlイオンと第4族元素を含む化合物または第4族元素のイオンとが反応して生成した反応生成物が、めっき層と化成処理皮膜の界面に濃化して、めっき鋼板の初期の耐食性および耐変色性を向上させる。 Further, the compound containing a Group 4 element or the ion of a Group 4 element also improves the film adhesion, the water resistance and the color fastness of the chemical conversion film. For example, when a chemical conversion treatment film is formed on the surface of an Al-containing Zn-based alloy plated steel sheet with an aqueous treatment liquid containing a compound containing a Group 4 element or an ion of a Group 4 element, strong Al present on the surface of the plated steel sheet It is possible to suppress the decrease in the film adhesion due to the oxide. In addition, when a chemical conversion film is formed on the surface of an Al-containing Zn-based alloy plated steel sheet with an aqueous treatment liquid containing a compound containing a Group 4 element or an ion of a Group 4 element, Al ions and The reaction product formed by the reaction of the compound containing Group 4 element or the ion of Group 4 element is concentrated at the interface between the plating layer and the chemical conversion film, thereby improving the initial corrosion resistance and color fastness of the plated steel sheet. Let
 水系処理液中の第4族元素を含む化合物または第4族元素のイオンの金属原子換算での含有量は、たとえば0.5g/Lとすることができるが、水系フッ素樹脂を十分に架橋させて化成処理皮膜の密着性をより高める観点からは、2g/L以上であることが好ましい。上記観点からは、第4族元素を含む化合物または第4族元素のイオンの含有量は、1g/L以上であることがより好ましく、2g/L以上であることがさらに好ましい。なお、化成処理皮膜が多孔質状となることによる、化成処理皮膜の加工性および耐候性の低下を抑制する観点からは、水系処理液中の第4族元素を含む化合物または第4族元素のイオンの含有量は、30g/L以下であることが好ましい。水系処理液中の第4族元素を含む化合物または第4族元素のイオンの金属原子換算での含有量は、蛍光X線分析装置を用いて測定することができる。 The content of the compound containing a Group 4 element or the ion of a Group 4 element in the aqueous treatment liquid in terms of metal atom can be, for example, 0.5 g / L, but the aqueous fluororesin is sufficiently crosslinked. It is preferable that it is 2 g / L or more from a viewpoint of improving the adhesiveness of a chemical conversion treatment film more. From the above viewpoint, the content of the ion of the compound containing the Group 4 element or the Group 4 element is more preferably 1 g / L or more, and still more preferably 2 g / L or more. From the viewpoint of suppressing the deterioration of the processability and the weatherability of the chemical conversion film due to the porous state of the chemical conversion film, the compound or element of the fourth group element in the aqueous treatment liquid is used. The content of ions is preferably 30 g / L or less. The content of the compound containing a Group 4 element or the ion of a Group 4 element in the aqueous treatment liquid in terms of metal atom can be measured using a fluorescent X-ray analyzer.
 1-3.結合促進剤
 結合促進剤は、水系処理液中に存在するフッ素樹脂を軟質化することができる。上記結合促進剤によって軟質化したフッ素樹脂は、エマルションを構成する粒子同士がより密に融着しやすくなり、より水を浸透しにくい化成処理皮膜を形成する。そのため、結合促進剤を含む上記水系処理液から形成された化成処理皮膜は赤錆を発生させにくくなり、化成処理皮膜の耐食性がより高まると考えられる。また、結合促進剤は、フッ素樹脂を軟質化してエマルションを構成する粒子同士をより密に融着しやすくすることにより、より紫外線などの光によって分解しにくい化成処理皮膜を形成する。そのため、結合促進剤を含む上記水系処理液から形成された化成処理皮膜は、耐候性もより高まると考えられる。
1-3. Bond promoter The bond promoter can soften the fluorine resin present in the aqueous treatment liquid. The fluorinated resin softened by the above-mentioned bonding promoter makes it easier for the particles constituting the emulsion to be more closely fused to each other, and forms a chemical conversion film which is more difficult to permeate water. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter does not easily generate rust, and the corrosion resistance of the chemical conversion treatment film is further enhanced. In addition, the bonding promoter softens the fluorocarbon resin to make the particles constituting the emulsion adhere more closely, thereby forming a chemical conversion film that is less likely to be decomposed by light such as ultraviolet light. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter further enhances the weather resistance.
 また、上記結合促進剤は、上述した作用により、常温程度でもフッ素樹脂をよく融着させることができる。そのため、上記結合促進剤を含む水系処理液は、加工現場などにおけるめっき鋼板の切断により生じる端面や、めっき鋼板の端面などの露出部位に、加工現場で加熱せずにより容易に化成処理皮膜を形成することができる。 Moreover, the said bonding promoter can fuse | melt a fluororesin well well also at about normal temperature by the effect | action mentioned above. Therefore, the aqueous treatment liquid containing the above-mentioned bond promoter easily forms a chemical conversion treatment film on the exposed surface such as the end face or the end face of the plated steel sheet caused by cutting of the plated steel sheet at the processing site etc. without heating at the processing site. can do.
 結合促進剤は、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンから適宜選択して用いることができる。このような結合促進剤の例には、ジメチルアジペート、ジエチルアジペート、ジ(イソ)プロピルアジペート、ジ(イソ)ブチルアジペート、ジメチルフタレート、ジエチルフタレート、ジ(イソ)プロピルフタレート、ジ(イソ)ブチルフタレート、およびn-メチル-2-ピロリドンが含まれる。これらの結合促進剤のうち、耐食性、処理外観の観点からは、ジメチルアジペート、ジエチルアジペート、ジ(イソ)プロピルアジペートおよびジ(イソ)ブチルアジペートが好ましい。なお、本発明において、(イソ)プロピルとは、プロピルおよびイソプロピルを意味し、(イソ)ブチルとは、ブチルおよびイソブチルを意味する。 The bonding accelerator can be appropriately selected from adipic acid or an ester compound of phthalic acid and an alcohol having 1 to 3 carbon atoms, and n-methyl-2-pyrrolidone. Examples of such binding promoters include dimethyl adipate, diethyl adipate, di (iso) propyl adipate, di (iso) butyl adipate, dimethyl phthalate, diethyl phthalate, di (iso) propyl phthalate, di (iso) butyl phthalate And n-methyl-2-pyrrolidone. Among these bonding promoters, dimethyl adipate, diethyl adipate, di (iso) propyl adipate and di (iso) butyl adipate are preferable from the viewpoint of corrosion resistance and appearance of processing. In the present invention, (iso) propyl means propyl and isopropyl, and (iso) butyl means butyl and isobutyl.
 水系処理液中の結合促進剤の含有量は、たとえば0.1g/L以上50g/L以下とすることができるが、上述した作用によりフッ素樹脂をより融着しやすくして、化成処理皮膜の耐食性をより高める観点からは、0.5g/L以上50g/L以下であることが好ましく、0.7g/L以上30g/L以下であることがより好ましく、1g/L以上15g/L以下であることがさらに好ましい。 The content of the bonding promoter in the aqueous treatment liquid can be, for example, 0.1 g / L or more and 50 g / L or less, but the fluorine resin can be more easily fused by the above-described action, From the viewpoint of further enhancing the corrosion resistance, it is preferably 0.5 g / L to 50 g / L, more preferably 0.7 g / L to 30 g / L, and 1 g / L to 15 g / L. It is further preferred that
 1-4.エッチング剤
 エッチング剤は、基材鋼板の表面を均一化および活性化して、化成処理皮膜の密着性をより高め、化成処理皮膜からめっき鋼板への水の浸透を抑制する。そのため、結合促進剤を含む上記水系処理液から形成された化成処理皮膜は赤錆を発生させにくくなり、化成処理皮膜の耐食性がより高まると考えられる。
1-4. Etchant The etchant uniforms and activates the surface of the base steel sheet to further enhance the adhesion of the chemical conversion coating and suppress the penetration of water from the chemical conversion coating to the plated steel sheet. Therefore, it is thought that the chemical conversion treatment film formed from the above-mentioned water-based processing solution containing a binding promoter does not easily generate rust, and the corrosion resistance of the chemical conversion treatment film is further enhanced.
 具体的には、エッチング剤は、めっき層に含まれるZnおよびAlおよび基材鋼板に含まれるFeなどの金属成分を溶解し、溶解した金属成分を化成処理皮膜中に取り込むことによって、化成処理皮膜が形成されためっき鋼板の耐食性を高める。このとき、本発明では、上記取り込まれた金属成分が、上述した結合促進剤によってエマルション状のフッ素樹脂のより内部にまで取り込まれて、化成処理皮膜の密着性もより高める結果、化成処理皮膜が形成されためっき鋼板の耐食性をより高めると考えられる。 Specifically, the etching agent dissolves metal components such as Zn and Al contained in the plating layer and Fe contained in the base steel plate, and incorporates the dissolved metal component into the chemical conversion treatment film to form a chemical conversion treatment film. Enhance the corrosion resistance of the plated steel sheet formed. At this time, in the present invention, the metal component taken in is taken into the inside of the emulsion-like fluorine resin by the above-mentioned bond promoter, and as a result, the adhesion of the chemical conversion treatment film is further enhanced. It is believed that the corrosion resistance of the formed plated steel sheet is further enhanced.
 特に、エッチング剤は、基材鋼板の露出部位を活性化する観点からは、リン酸またはリン酸塩、およびアンモニアまたはアンモニウム塩が好ましい。 In particular, from the viewpoint of activating the exposed site of the base steel plate, the etchant is preferably phosphoric acid or phosphate, and ammonia or ammonium salt.
 リン酸またはリン酸塩は、基材鋼板の露出部位における鉄(Fe)や、Zn系めっきに含まれる亜鉛(Zn)を均一化および活性化する。そのため、リン酸またはリン酸塩は、鋼板およびZn系めっき鋼板に特に有用である。 Phosphoric acid or phosphate homogenizes and activates iron (Fe) at the exposed portion of the base steel plate or zinc (Zn) contained in Zn-based plating. Therefore, phosphoric acid or phosphate is particularly useful for steel plates and Zn-based plated steel plates.
 リン酸またはリン酸塩は、リン酸アニオン(PO 3-)を有する水溶性の化合物であればよい。リン酸塩の例には、リン酸ナトリウム、リン酸アンモニウム、リン酸水素アンモニウム、リン酸二水素アンモニウム、リン酸マグネシウム、リン酸カリウム、リン酸マンガン、リン酸亜鉛、オルトリン酸、メタリン酸、ピロリン酸、三リン酸、および四リン酸などが含まれる。これらのリン酸またはリン酸塩は、単独で使用されてもよいし、2種類以上を組み合わせて使用されてもよい。 The phosphoric acid or phosphate may be a water-soluble compound having a phosphate anion (PO 4 3- ). Examples of phosphates include sodium phosphate, ammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, magnesium phosphate, potassium phosphate, manganese phosphate, zinc phosphate, orthophosphoric acid, metaphosphoric acid, pyrroline Acids, triphosphates, tetraphosphates and the like are included. These phosphoric acids or phosphates may be used alone or in combination of two or more.
 アンモニア酸またはアンモニウム塩は、基材鋼板の露出部位における鉄(Fe)や、Al系めっきやZn-Al系めっきに含まれるアルミニウム(Al)を均一化および活性化する。そのため、リン酸またはリン酸塩は、鋼板およびZn-Al系めっき鋼板に特に有用である。 The ammonia acid or ammonium salt homogenizes and activates iron (Fe) at the exposed portion of the base steel plate, or aluminum (Al) contained in Al-based plating or Zn—Al-based plating. Therefore, phosphoric acid or phosphate is particularly useful for steel plates and Zn-Al-based plated steel plates.
 アンモニウム塩の例には、第四級アンモニウムカチオン(NH )のリン酸塩、フッ化物および金属塩などが含まれる。これらのうち、第四級アンモニウムカチオンのリン酸塩を含むことが好ましく、リン酸アンモニウム、リン酸水素アンモニウムおよびリン酸二水素アンモニウムを含むことがより好ましい。 Examples of ammonium salts include phosphates, fluorides and metal salts of quaternary ammonium cations (NH 4 + ) and the like. Among these, it is preferable to contain the phosphate of a quaternary ammonium cation, and it is more preferable to contain ammonium phosphate, ammonium hydrogen phosphate and ammonium dihydrogen phosphate.
 なお、単一の水系処理液で様々な鋼板やめっき鋼板(Zn系、Al系、Zn-Al系、およびZn-Al-Mg系など)に適用可能にする観点からは、水系処理液は、リン酸またはリン酸塩と、アンモニアまたはアンモニウム塩と、の双方を含むことが好ましい。また、基材鋼板の表面を均一化および活性化する効果をより高め、化成処理皮膜の耐候性をより高める観点からも、水系処理液は、リン酸またはリン酸塩と、アンモニアまたはアンモニウム塩と、の双方を含むことが好ましい。これらの観点からは、エッチング剤は、第四級アンモニウムカチオンのリン酸塩が好ましく、リン酸アンモニウム、リン酸水素アンモニウムおよびリン酸二水素アンモニウムがより好ましい。 From the viewpoint of making it applicable to various steel plates and plated steel plates (such as Zn-based, Al-based, Zn-Al-based, and Zn-Al-Mg-based) with a single aqueous processing liquid, the aqueous processing liquid is It is preferred to include both phosphoric acid or phosphate and ammonia or ammonium salt. In addition, from the viewpoint of further enhancing the effect of homogenizing and activating the surface of the base steel plate and further improving the weather resistance of the chemical conversion film, the aqueous treatment liquid comprises phosphoric acid or phosphate and ammonia or ammonium salt. It is preferable to include both of. From these viewpoints, the etchant is preferably a phosphate of quaternary ammonium cation, more preferably ammonium phosphate, ammonium hydrogen phosphate and ammonium dihydrogen phosphate.
 水系処理液中のエッチング剤の含有量は、リン酸アニオン(PO 3-)の含有量が、リン酸アニオン換算で、1g/L以上であることが好ましく、2g/L以上であることがさらに好ましい。あるいは、水系処理液中のエッチング剤の含有量は、第四級アンモニウムカチオン(NH )の含有量が、第四級アンモニウムカチオン換算で、1g/L以上であることが好ましく、2g/L以上であることがさらに好ましい。 Regarding the content of the etching agent in the aqueous treatment liquid, the content of the phosphate anion (PO 4 3- ) is preferably 1 g / L or more, and 2 g / L or more in terms of phosphate anion. More preferable. Alternatively, regarding the content of the etching agent in the aqueous treatment liquid, the content of the quaternary ammonium cation (NH 4 + ) is preferably 1 g / L or more in terms of the quaternary ammonium cation, and 2 g / L. It is more preferable that it is more than.
 水系処理液中のエッチング剤の含有量は、エッチング剤がリン酸またはリン酸塩とアンモニアまたはアンモニウム塩との双方を含むときは、リン酸アニオン(PO 3-)および第四級アンモニウムカチオン(NH )の含有量が、それぞれリン酸アニオン換算および第四級アンモニウムカチオン換算で、いずれも1g/L以上であることが好ましく、2g/L以上であることがさらに好ましい。 The content of the etching agent in the aqueous processing solution is such that, when the etching agent contains both phosphoric acid or phosphate and ammonia or ammonium salt, phosphate anion (PO 4 3- ) and quaternary ammonium cation ( The content of NH 4 + ) is preferably 1 g / L or more, and more preferably 2 g / L or more, in terms of phosphate anion and quaternary ammonium cation, respectively.
 1-5.シランカップリング剤
 シランカップリング剤は、化成処理皮膜の密着性をより高める。
1-5. Silane Coupling Agent The silane coupling agent further improves the adhesion of the chemical conversion film.
 水系処理液中のシランカップリング剤の含有量は、フッ素樹脂100質量部に対して、0.5質量部以上5質量部以下であることが好ましい。シランカップリング剤の含有量が0.5質量部以上であると、化成処理皮膜の密着性をより高めることができる。一方、シランカップリング剤の含有量が5質量部以下であると、水系処理液の保存安定性の低下を抑制できる。 The content of the silane coupling agent in the aqueous treatment liquid is preferably 0.5 parts by mass to 5 parts by mass with respect to 100 parts by mass of the fluorocarbon resin. The adhesiveness of a chemical conversion treatment film can be improved more as content of a silane coupling agent is 0.5 mass part or more. On the other hand, when the content of the silane coupling agent is 5 parts by mass or less, a decrease in the storage stability of the aqueous treatment liquid can be suppressed.
 1-6.その他の成分
 水系処理液は、その他の成分として、上述以外の無機化合物、シランカップリング剤以外の有機潤滑剤、無機潤滑剤、無機顔料、有機顔料、および染料などを必要に応じて添加してもよい。Mg、Ca、Sr、V、W、Mn、B、Si、Snなどの無機化合物(酸化物、リン酸塩など)は、化成処理皮膜を緻密化して耐水性を向上させる。フッ素系、ポリエチレン系、およびスチレン系などの有機潤滑剤、ならびに二硫化モリブデンおよびタルクなどの無機潤滑剤は、化成処理皮膜の潤滑性を向上させる。また、無機顔料、有機顔料、および染料などを配合することで、化成処理皮膜に所定の色調を付与することができる。
1-6. Other Components The aqueous treatment liquid may contain, as other components, inorganic compounds other than those described above, organic lubricants other than silane coupling agents, inorganic lubricants, inorganic pigments, organic pigments, dyes, etc., as necessary. It is also good. Inorganic compounds (oxides, phosphates, etc.) such as Mg, Ca, Sr, V, W, Mn, B, Si, Sn etc. densify the chemical conversion film to improve water resistance. Organic lubricants such as fluorine, polyethylene, and styrene, and inorganic lubricants such as molybdenum disulfide and talc improve the lubricity of the chemical conversion film. Moreover, a predetermined | prescribed color tone can be provided to a chemical conversion treatment film by mix | blending an inorganic pigment, an organic pigment, and dye.
 なお、水系処理液は、バナジウム(V)イオンおよびチタン(Ti)イオンの含有量が、金属原子換算で500ppm以下であることが好ましい。VやTiを含む化合物は、防錆剤として用いられることがあるが、これらのイオンの含有量をより少なくすることで、VやTiの光触媒作用による化成処理皮膜の耐候性の低下を抑制することができる。 In addition, it is preferable that content of vanadium (V) ion and titanium (Ti) ion is 500 ppm or less in conversion of a metal atom in a water-based process liquid. Compounds containing V or Ti may be used as a rust inhibitor, but by reducing the content of these ions, the decrease in the weatherability of the chemical conversion treatment film due to the photocatalytic action of V or Ti is suppressed be able to.
 また、水系処理液は、クロム(Cr)、特には6価クロム、の含有量が、金属原子換算で100ppm以下であることが好ましい。Cr(6価クロム)の含有量をより少なくすることで、人体への影響が少なく、安全性の高い化成処理皮膜を形成することができる。 Further, in the aqueous treatment liquid, the content of chromium (Cr), particularly hexavalent chromium, is preferably 100 ppm or less in terms of metal atom. By further reducing the content of Cr (hexavalent chromium), it is possible to form a highly safe chemical conversion film with less influence on the human body.
 また、水系処理液は、クリアな皮膜を形成する観点から、無機顔料、有機顔料、および染料などを実質的に含まないことが好ましい。水系処理液は、フッ素樹脂を主成分とするため、リン酸のマンガンまたは鉄などの塩によりリン酸塩皮膜を形成するリン酸塩処理(パーカライジング)や、多量の亜鉛粉末により犠牲防食層を形成するジンクリッチペイントとは異なり、クリアな皮膜を形成することができる。 In addition, from the viewpoint of forming a clear film, the aqueous treatment liquid preferably contains substantially no inorganic pigment, organic pigment, dye, and the like. Since the aqueous treatment liquid contains a fluorine resin as a main component, a phosphate treatment (percuralizing) to form a phosphate film with a salt of phosphoric acid such as manganese or iron, or a large amount of zinc powder forms a sacrificial anticorrosive layer Unlike zinc-rich paint, it can form clear films.
 1-7.水系処理液の性状
 水系処理液は、水などの溶媒を除く固形分の含有量(固形分濃度)が、水系処理液の全質量に対して20質量%以上であることが好ましい。固形分の含有量が20質量%以上であると、十分な膜厚を有し、十分な耐候性を有する化成処理皮膜を形成できる。なお、固形分の含有量の上限は処理液安定性の面から、40質量%以下であることが好ましい。
1-7. Properties of Aqueous Treatment Liquid The aqueous treatment liquid preferably has a solid content (solid content concentration) excluding a solvent such as water of 20% by mass or more based on the total mass of the aqueous treatment liquid. When the solid content is 20% by mass or more, a chemical conversion film having a sufficient film thickness and a sufficient weather resistance can be formed. In addition, it is preferable that the upper limit of content of solid content is 40 mass% or less from the surface of process liquid stability.
 水系処理液は、pHが7.0以上9.5以下であることが好ましい。pHが7.0以上であると、Znのエッチング量を適度に調整でき、pHが9.5以下であると、Alのエッチング量を適度に調整できる。そのため、pHが7.0以上9.5以下であると、過剰なエッチングによる外観不良または耐食性の低下を抑制できる。 The aqueous treatment liquid preferably has a pH of 7.0 or more and 9.5 or less. When the pH is 7.0 or more, the etching amount of Zn can be appropriately adjusted, and when the pH is 9.5 or less, the etching amount of Al can be appropriately adjusted. Therefore, when the pH is 7.0 or more and 9.5 or less, the appearance defect due to excessive etching or the deterioration of the corrosion resistance can be suppressed.
 水系処理液は、1液型でもよいし、フッ素樹脂のエマルションと結合促進剤を含む溶液(または分散液)とを使用時に混合する2液混合型でもよい。 The aqueous treatment liquid may be a one-component type, or a two-component mixture type in which an emulsion of a fluorocarbon resin and a solution (or dispersion liquid) containing a bonding accelerator are mixed at the time of use.
 2.めっき鋼板の化成処理方法
 上述した水系処理液は、めっき鋼板の化成処理に用いることができる。具体的には、上述した水系処理液を、めっき鋼板の端面に付与し、乾燥させて、化成処理皮膜を形成することができる。
2. The chemical conversion treatment method of a plated steel plate The above-mentioned aqueous treatment liquid can be used for the chemical conversion treatment of a plated steel plate. Specifically, the above-mentioned aqueous treatment liquid can be applied to the end face of the plated steel sheet and dried to form a chemical conversion treatment film.
 めっきが施される基材鋼板の種類は、特に限定されない。たとえば、鋼板は、低炭素鋼、中炭素鋼および高炭素鋼などを含む炭素鋼でもよいし、Mn、Cr、Si、Niなどを含有する合金鋼でもよい。また、鋼板は、Alキルド鋼などを含むキルド鋼でもよいし、リムド鋼でもよい。良好なプレス成形性が必要とされる場合は、低炭素Ti添加鋼および低炭素Nb添加鋼などを含む深絞り用鋼板が鋼板として好ましい。また、P、Si、Mnなどの量を特定の値に調整した高強度鋼板を用いてもよい。 The type of base steel plate to be plated is not particularly limited. For example, the steel plate may be a carbon steel including low carbon steel, medium carbon steel, high carbon steel and the like, or an alloy steel containing Mn, Cr, Si, Ni and the like. The steel plate may be a killed steel including Al-killed steel or the like, or may be a rimmed steel. When good press formability is required, deep drawing steel sheets including low carbon Ti-added steel and low carbon Nb-added steel are preferable as steel sheets. Further, a high strength steel plate in which the amounts of P, Si, Mn, etc. are adjusted to specific values may be used.
 めっき鋼板は、上記鋼板を基材鋼板とし、公知のめっきを施したものであればよい。めっきは、溶融めっきでも蒸着めっきでもよい。めっきの種類は、特に限定されず、Zn系めっき(Znめっき、Zn-Alめっき、およびZn-Al-Mgめっきなど)、Al系めっき、ならびにNi系めっきなどを使用することができる。これらのうち、Zn系めっきおよびAl系めっきが好ましく、Zn系めっきがより好ましい。 The plated steel plate may be made of any of the above steel plates as a base steel plate and subjected to known plating. The plating may be hot-dip plating or vapor deposition plating. The type of plating is not particularly limited, and Zn-based plating (Zn plating, Zn-Al plating, Zn-Al-Mg plating, etc.), Al-based plating, Ni-based plating, etc. can be used. Among these, Zn-based plating and Al-based plating are preferable, and Zn-based plating is more preferable.
 上述した水系処理液は、各種めっき層および基材鋼板の双方に密着性が高い化成処理皮膜を形成できるため、めっき鋼板のうち、その端面や、切断により生じる端面などの、基材鋼板が露出した部位に付与し、乾燥させて、化成処理皮膜を形成することができる。 The aqueous treatment liquid described above can form a chemical conversion film having high adhesion to both the various plating layers and the base steel plate, so among the plated steel plates, the base steel plate such as the end face or the end face generated by cutting is exposed The chemical conversion treatment film can be formed by applying to the above-described site and drying.
 また、めっき鋼板には、公知の方法でプレコートの下地化成処理が施されていてもよい。 In addition, the plated steel sheet may be subjected to a base chemical conversion treatment of a precoat by a known method.
 水系処理液の塗布方法は、特に限定されず、めっき鋼板の形状などに応じて適宜選択すればよい。塗布方法の例には、ロールコート法、カーテンフロー法、スピンコート法、スプレー法、浸漬引き上げ法、および滴下法などが含まれる。水系処理液の液膜の厚さは、フェルト絞りやエアワイパーなどにより調整することができる。 The application method of the aqueous treatment liquid is not particularly limited, and may be appropriately selected according to the shape of the plated steel sheet and the like. Examples of the coating method include roll coating, curtain flow, spin coating, spraying, immersion pulling, and dropping. The thickness of the liquid film of the aqueous treatment liquid can be adjusted by a felt throttle, an air wiper, or the like.
 水系処理液の塗布量は、特に限定されないが、化成処理皮膜の膜厚が0.5μm以上10μm以下となるように調整されることが好ましい。化成処理皮膜の膜厚が0.5μm以上であると、化成処理皮膜に耐候性、耐食性および耐変色性などを十分に付与することができる。一方、膜厚を10μm超としても、膜厚の増加に伴う性能向上を期待することはできない。 Although the application amount of the aqueous treatment liquid is not particularly limited, it is preferable to adjust the film thickness of the chemical conversion treatment film to be 0.5 μm or more and 10 μm or less. When the film thickness of the chemical conversion film is 0.5 μm or more, the chemical conversion film can be sufficiently imparted with weather resistance, corrosion resistance, color fastness and the like. On the other hand, even if the film thickness is more than 10 μm, it can not be expected to improve the performance accompanying the increase of the film thickness.
 付与された水系処理液は、常温で乾燥させて、化成処理皮膜とすることができる。なお、付与された水系処理液を加熱(たとえば50℃以上に加熱)して乾燥させてもよいが、このとき、有機成分の熱分解による化成処理皮膜の性能低下を抑制する観点からは、乾燥温度は300℃以下であることが好ましい。なお、加工現場などにおいて、めっき鋼板の切断により生じる端面や、めっき鋼板の端面などの基材鋼板の露出部位に、より容易に化成処理皮膜を形成する観点からは、常温で乾燥させることが好ましい。 The applied aqueous treatment liquid can be dried at normal temperature to form a chemical conversion treatment film. The applied aqueous treatment liquid may be dried by heating (for example, heating to 50 ° C. or higher), but from this point of view, drying is performed from the viewpoint of suppressing the performance deterioration of the chemical conversion treatment film due to the thermal decomposition of the organic component. The temperature is preferably 300 ° C. or less. In addition, it is preferable to dry at normal temperature from the viewpoint of forming a chemical conversion treatment film more easily on exposed portions of the base steel plate such as an end face generated by cutting a plated steel plate and an end face of a plated steel plate .
 3.化成処理鋼板および成形加工品
 上述の水系処理液から形成された化成処理皮膜を有する化成処理鋼板は、上述のめっき鋼板と、上記めっき鋼板の端面、好ましくは上記めっき鋼板の端面の基材鋼板が露出した部位、を被覆するように形成された上記化成処理皮膜と、を有する。上記化成処理鋼板は、成形加工品であってもよい。成形加工の方法は特に限定されず、プレス加工、抜き加工および絞り加工などの公知の方法から選択することができる。
3. Chemically-treated steel sheet and molded processed product A chemically-treated steel sheet having a chemical conversion film formed from the above-mentioned aqueous treatment liquid comprises the above-mentioned plated steel sheet and the base steel plate of the end face of the above-mentioned plated steel sheet, preferably the end face of the above-mentioned plated steel plate And the above-described chemical conversion treatment film formed to cover the exposed portion. The chemical conversion treated steel sheet may be a molded processed product. The method of forming is not particularly limited, and can be selected from known methods such as pressing, punching and drawing.
 より具体的には、上記化成処理皮膜は、上述のフッ素樹脂を含む有機樹脂と、上述の第4族元素を含む化合物または第4族元素のイオンと、アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、シランカップリング剤と、を含む。 More specifically, the above-mentioned chemical conversion film comprises an organic resin containing the above-mentioned fluororesin, a compound containing the above-mentioned Group 4 element or an ion of the Group 4 element, adipic acid or phthalic acid, and one or more carbon atoms. And at least one bond promoter selected from the group consisting of an ester compound with an alcohol of 3 or less and n-methyl-2-pyrrolidone, and a silane coupling agent.
 これらの成分の含有量比は、水系処理液について上述した比率と同様である。 The content ratio of these components is the same as the ratio described above for the aqueous treatment liquid.
 化成処理皮膜の膜厚は、0.5μm以上10μm以下であることが好ましい。膜厚が0.5μm以上であると、化成処理皮膜に耐候性、耐食性および耐変色性などを十分に付与することができる。一方、膜厚を10μm超としても、膜厚の増加に伴う性能向上を期待することはできない。 It is preferable that the film thickness of a chemical conversion treatment film is 0.5 micrometer or more and 10 micrometers or less. When the film thickness is 0.5 μm or more, the chemical conversion film can be sufficiently provided with weather resistance, corrosion resistance, discoloration resistance, and the like. On the other hand, even if the film thickness is more than 10 μm, it can not be expected to improve the performance accompanying the increase of the film thickness.
 この化成処理鋼板は、耐候性、特には長期の耐候性に優れる。また、めっき鋼板の成形加工などにより生じる基材鋼板の露出部位である端面などに、上記化成処理皮膜を有する化成処理鋼板は、上記基材鋼板の露出部位などにおける化成処理皮膜の耐候性、特には長期の耐候性に優れるため好ましい。また、上述したように、めっき層を溶かして溶接加工した溶接部に上記化成処理皮膜を有する化成処理鋼板は、溶接部の耐食性が高まる効果が顕著にみられる。 The chemically treated steel sheet is excellent in weatherability, particularly long-term weatherability. In addition, the chemically treated steel sheet having the above-mentioned chemical conversion treatment film on the end face or the like which is the exposed portion of the base steel plate produced by the forming process of the plated steel plate etc. Is preferable because it is excellent in long-term weather resistance. In addition, as described above, the chemically treated steel sheet having the above-mentioned conversion treated film on the weld formed by melting and plating the plating layer has a remarkable effect of enhancing the corrosion resistance of the weld.
 以下、実施例を参照して本発明を詳細に説明するが、本発明はこれらの実施例により限定されない。 Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not limited by these examples.
 1.水系処理液の調製
 各成分を混合して、表1に示す水系処理液1~水系処理液15を調製した。
1. Preparation of Aqueous Treatment Solution The components were mixed to prepare aqueous treatment solution 1 to aqueous treatment solution 15 shown in Table 1.
 なお、フッ素樹脂(FR)は、フッ素系樹脂(Tg:-35~25℃、最低成膜温度(MFT):10℃)の水系エマルションを使用した。上記フッ素樹脂エマルションの固形分濃度は38質量%であり、フッ素樹脂中のフッ素原子の含有量は25質量%であり、エマルションの平均粒径は150nmであった。 As the fluorine resin (FR), an aqueous emulsion of fluorine resin (Tg: -35 to 25 ° C., minimum film forming temperature (MFT): 10 ° C.) was used. The solid content concentration of the fluororesin emulsion was 38% by mass, the content of fluorine atoms in the fluororesin was 25% by mass, and the average particle diameter of the emulsion was 150 nm.
 アクリル樹脂(AR)は、アクリル樹脂エマルションである、DIC株式会社製の「パテラコール」(「パテラコール」は同社の登録商標)を用意した。「パテラコール」の固形分濃度は40質量%であり、エマルションの平均粒径は10~100nm程度と思われた。 Acrylic resin (AR) is an acrylic resin emulsion, "Patellacole" ("Patellacole" is a registered trademark of the company) manufactured by DIC Corporation. The solid content concentration of "pateracol" was 40% by mass, and the average particle size of the emulsion appeared to be about 10 to 100 nm.
 ウレタン樹脂(PU)は、ウレタン樹脂エマルションである、DIC株式会社製の「ハイドラン」を使用した。「ハイドラン」の固形分濃度は35質量%であり、エマルションの平均粒径は10~100nm程度と思われた。 As a urethane resin (PU), "Hydran" manufactured by DIC Corporation, which is a urethane resin emulsion, was used. The solid content concentration of "Hydran" was 35% by mass, and the average particle size of the emulsion appeared to be about 10 to 100 nm.
 エッチング剤については、リン酸量は、リン酸、リン酸水素二アンモニウムおよびリン酸二水素アンモニウムの合計量で調整し、アンモニウム量は、アンモニア(水溶液)、炭酸ジルコニウムアンモニウム、フッ化ジルコニウムアンモニウム、リン酸水素二アンモニウム、リン酸二水素アンモニウムおよび炭酸アンモニウムの合計量で調整した。 For the etching agent, the amount of phosphoric acid is adjusted by the total amount of phosphoric acid, diammonium hydrogen phosphate and ammonium dihydrogen phosphate, and the amount of ammonium is ammonia (aqueous solution), zirconium ammonium carbonate, zirconium ammonium fluoride, phosphorus The total amount of diammonium hydrogen oxide, ammonium dihydrogen phosphate and ammonium carbonate was adjusted.
 シランカップリング剤(SCA)は、モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社製の「SILQUEST  A-186」を使用した。 As the silane coupling agent (SCA), “SILQUEST A-186” manufactured by Momentive Performance Materials Japan Ltd. was used.
 なお、表1の「F量」、「Zr量」、「添加量」、「リン酸量」、「アンモニウム量」および「SCA添加量」は、それぞれ、フッ素原子の量(質量%)、第4族元素を含む化合物または第4族元素のイオンの金属原子換算での量(g/L)、結合促進剤の添加量(g/L)、リン酸またはリン酸塩のリン酸アニオン換算での含有量(g/L)、アンモニアまたはアンモニウム塩の第四級アンモニウムカチオン換算での含有量(g/L)、およびシランカップリング剤の添加量(フッ素樹脂の質量を100質量%としたときの添加量)を示す。 The “F amount”, “Zr amount”, “addition amount”, “phosphoric acid amount”, “ammonium amount” and “SCA addition amount” in Table 1 are respectively the amount (% by mass) of fluorine atoms, Amount (g / L) of metal containing compound of Group 4 element or ion of Group 4 element in terms of metal atom, added amount of bonding accelerator (g / L), conversion to phosphate anion of phosphoric acid or phosphate Content (g / L), content of the ammonia or ammonium salt in terms of quaternary ammonium cation (g / L), and addition amount of the silane coupling agent (when the mass of the fluorine resin is 100% by mass) Added amount of
 また、表1の「有機樹脂」の「種類」に「FR/AR」と記載されているときは、上記フッ素樹脂と上記アクリル樹脂とをブレンドして、他の化合物とあわせた水系処理液中の固形分量が「固形分量」に記載の数値になり、かつ、フッ素原子の量が「F量」に記載の数値になるように調整したことを示す。 In addition, when “FR / AR” is described in “Type” of “organic resin” in Table 1, the above-mentioned fluororesin and the above-mentioned acrylic resin are blended, and it is in the aqueous treatment liquid combined with other compounds. The solid content of the solid content is the numerical value described in “solid content”, and the amount of fluorine atoms is adjusted to be the numerical value described in the “F amount”.
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
 2.評価
 水系処理液1~水系処理液15の保存安定性および水系処理液1~水系処理液15から形成した皮膜の端面部耐食性を、以下の基準で評価した。
2. Evaluation The storage stability of the aqueous treatment liquid 1 to the aqueous treatment liquid 15 and the corrosion resistance of the end face of the film formed from the aqueous treatment liquid 1 to the aqueous treatment liquid 15 were evaluated based on the following criteria.
 2-1.保存安定性
 水系処理液1~水系処理液15を常温で180日間保管した。各水系処理液の保管前後の粘度変化量(保管後粘度から保管前粘度を差し引いた値)をフォードカップNo.4により測定し、以下の基準で保存安定性を評価した。
 A 粘度変化量は10秒未満だった
 B 粘度変化量は10秒以上だったが、使用に問題はなかった
 C 粘度変化量は30秒以上であり、増粘により塗布が困難だった
2-1. Storage stability Aqueous treatment solution 1 to aqueous treatment solution 15 were stored at normal temperature for 180 days. The amount of change in viscosity (the value obtained by subtracting the viscosity before storage from the viscosity after storage) before and after storage of each aqueous treatment liquid was measured using Ford Cup No. 4, and storage stability was evaluated based on the following criteria.
A The change in viscosity was less than 10 seconds. The change in viscosity was 10 seconds or more, but there was no problem in use. The change in viscosity was 30 seconds or more. Coating was difficult due to thickening.
 2-2.端面部耐食性
 板厚0.6mmの普通鋼の表面に溶融Zn-6.0質量%Al-3.0質量%Mgめっき層(めっき付着量90g/m)を形成して、めっき鋼板とした。このめっき鋼板を幅50mm、長さ100mmに切り出したところ、切断により生じた端面の表面のうち約20%の面積がめっき層で覆われており、残りの約80%の面積は下地鋼が露出していた。
2-2. End surface corrosion resistance Hot-dip Zn-6.0 mass% Al-3.0 mass% Mg plating layer (coating adhesion amount 90 g / m 2 ) was formed on the surface of ordinary steel with a thickness of 0.6 mm to make a plated steel sheet . When this plated steel sheet is cut into a width of 50 mm and a length of 100 mm, about 20% of the surface of the end face generated by cutting is covered with the plating layer, and the remaining about 80% of the surface is exposed to the base steel Was.
 上記めっき鋼板の上記端面に、10ml/mの水系処理液1~水系処理液15を塗布し、常温で乾燥させて、試験片とした。 10 ml / m 2 of aqueous treatment solution 1 to aqueous treatment solution 15 were applied to the end face of the plated steel plate, and dried at normal temperature to obtain test pieces.
 試験片を大気に2年間暴露して、1年経過後および2年経過後に、試験片端面に発生した赤錆の面積率を測定し、端面の全面積のうち赤錆発生面積率WR(赤錆が発生した面積/端面全面積)を求めて、以下の基準で端面部耐食性を評価した。
 A  赤錆発生面積率WRは10%以下だった
 B  赤錆発生面積率WRは10%超30%以下だった
 C  赤錆発生面積率WRは30%超50%以下だった
 D  赤錆発生面積率WRは50%超だった
The test piece is exposed to the atmosphere for 2 years, and after 1 and 2 years, the area ratio of red rust generated on the end face of the test piece is measured, and the red rust generation area rate WR (red rust is generated The end surface corrosion resistance was evaluated based on the following criteria.
A Red rusting area ratio WR was less than 10% B Red rusting area ratio WR was more than 10% and 30% or less C Red rusting area ratio WR was more than 30% and 50% or less D Red rusting area ratio WR was 50 It was over%
 水系処理液1~水系処理液15の保存安定性および端面部耐食性の評価結果を、表2に示す。 Table 2 shows the evaluation results of storage stability and corrosion resistance of the end face portion of the aqueous treatment liquid 1 to the aqueous treatment liquid 15.
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
 フッ素樹脂を含む有機樹脂と、第4族元素を含む化合物または第4族元素のイオンと、エッチング剤と、結合促進剤と、を含む水系処理液1~水系処理液10は、水系処理液の保存安定性および形成された化成処理皮膜の耐食性がいずれも良好であった。 The aqueous treatment liquid 1 to aqueous treatment liquid 10 containing an organic resin containing a fluorine resin, a compound containing a Group 4 element or an ion of a Group 4 element, an etching agent, and a bonding accelerator The storage stability and the corrosion resistance of the formed chemical conversion film were all good.
 また、エッチング剤として、リン酸またはリン酸塩と、アンモニアまたはアンモニウム塩と、をいずれも含む水系処理液4~水系処理液10を用いて化成処理皮膜を形成すると、耐食性がさらに高くなった。 Further, when the chemical conversion treatment film is formed using the aqueous treatment solutions 4 to 10 containing any of phosphoric acid or phosphate and ammonia or ammonium salt as an etching agent, the corrosion resistance is further enhanced.
 一方で、フッ素樹脂以外の樹脂を含む水系処理液11~水系処理液13を用いて化成処理皮膜を形成すると、耐候性および耐食性が低かった。 On the other hand, when the chemical conversion treatment film was formed using the aqueous treatment solution 11 to the aqueous treatment solution 13 containing a resin other than the fluorine resin, the weather resistance and the corrosion resistance were low.
 また、第4族元素を含む化合物または第4族元素のイオンを含まない水系処理液14を用いて化成処理皮膜を形成すると、密着性が低かった。 In addition, when a chemical conversion treatment film is formed using the aqueous treatment liquid 14 which does not contain a compound containing a Group 4 element or an ion of a Group 4 element, the adhesion is low.
 また、結合促進剤を含まない水系処理液15を用いて化成処理皮膜を形成すると、耐食性が低かった。 Moreover, when a chemical conversion treatment film was formed using the aqueous | water-based processing liquid 15 which does not contain a binding promoter, corrosion resistance was low.
 本出願は、2018年1月24日出願の日本国出願番号2018-009507号に基づく優先権を主張する出願であり、当該出願の特許請求の範囲、および明細書に記載された内容は本出願に援用される。 This application is an application claiming priority based on Japanese Patent Application No. 2018-009507 filed on Jan. 24, 2018, the claims of the application, and the contents described in the specification are the present application. Incorporated by reference.
 本発明の水系処理液により製造される化成処理皮膜は、めっき鋼板のうち、成形加工等により基材鋼板が露出した端面における耐食性をより高めることができる。たとえば、本発明の水系処理液は、1)ビニールハウスまたは農業ハウス用の鋼管、形鋼、支柱、梁、搬送用部材、2)遮音壁、防音壁、吸音壁、防雪壁、ガードレール、高欄、防護柵、支柱、3)鉄道車両用部材、架線用部材、電気設備用部材、安全環境用部材、構造用部材、太陽光架台などの用途に使用するめっき鋼板へのポストコートによる化成処理皮膜の形成に好適に使用されうる。
 
The chemical conversion film produced by the aqueous treatment liquid of the present invention can further enhance the corrosion resistance at the end face of the plated steel plate where the base steel plate is exposed by the forming process and the like. For example, the aqueous treatment liquid of the present invention is 1) steel pipes for steel or agricultural houses, shaped steels, columns, beams, conveying members, 2) sound insulation walls, sound insulation walls, sound absorption walls, snow protection walls, guard rails, balustrades, protection Rails, columns, 3) Rail vehicle members, wire members, members for electrical equipment, members for safety environment, members for construction, structural members, formation of a chemical conversion film by post coating on plated steel plates used for applications such as solar mounts Can be suitably used.

Claims (14)

  1.  フッ素樹脂を含む有機樹脂と、
     第4族元素を含む化合物または第4族元素のイオンと、
     エッチング剤と、
     アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、
     シランカップリング剤と、
     を含む、めっき鋼板の端面防錆処理液。
    An organic resin containing a fluorine resin,
    A compound containing a Group 4 element or an ion of a Group 4 element;
    An etchant,
    An ester compound of adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms, and at least one bond promoter selected from the group consisting of n-methyl-2-pyrrolidone,
    With a silane coupling agent,
    End surface rustproofing solution for plated steel sheet, including
  2.  前記フッ素樹脂は、前記フッ素樹脂の全質量に対して6質量%以上のフッ素原子を含む、請求項1に記載のめっき鋼板の端面防錆処理液。 The end surface rustproofing solution for a plated steel plate according to claim 1, wherein the fluorine resin contains 6% by mass or more of fluorine atoms with respect to the total mass of the fluorine resin.
  3.  前記第4族元素を含む化合物または第4族元素のイオンの含有量は、金属原子換算で2g/L以上である、請求項1または2に記載のめっき鋼板の端面防錆処理液。 The end surface rustproofing solution for a plated steel plate according to claim 1 or 2, wherein the content of the compound containing a Group 4 element or the ion of a Group 4 element is 2 g / L or more in terms of metal atom.
  4.  前記結合促進剤の含有量は、0.5g/L以上50g/L以下である、請求項1~3のいずれか1項に記載のめっき鋼板の端面防錆処理液。 The end face rustproofing solution for a plated steel plate according to any one of claims 1 to 3, wherein a content of the bonding promoter is 0.5 g / L to 50 g / L.
  5.  リン酸およびリン酸塩、ならびにアンモニアおよびアンモニウム塩、からなる群から選択されるエッチング剤をさらに含む、請求項1~4のいずれか1項に記載のめっき鋼板の端面防錆処理液。 The end face rustproofing solution for a plated steel sheet according to any one of claims 1 to 4, further comprising an etching agent selected from the group consisting of phosphoric acid and phosphate, and ammonia and ammonium salt.
  6.  前記エッチング剤は、リン酸またはリン酸塩と、アンモニアまたはアンモニウム塩と、をいずれも含む、請求項5に記載のめっき鋼板の端面防錆処理液。 The end face rustproofing solution for a plated steel sheet according to claim 5, wherein the etching agent contains any of phosphoric acid or phosphate and ammonia or ammonium salt.
  7.  前記リン酸またはリン酸塩の含有量は、リン酸アニオン(PO 3-)換算で1g/L以上であり、かつ、前記アンモニアまたはアンモニウム塩の含有量は、第四級アンモニウムカチオン(NH )換算で1g/L以上である、請求項6に記載のめっき鋼板の端面防錆処理液。 The content of the phosphoric acid or phosphate is 1 g / L or more in terms of phosphate anion (PO 4 3- ), and the content of the ammonia or ammonium salt is a quaternary ammonium cation (NH 4 The end face rustproofing solution of the plated steel plate according to claim 6, which is 1 g / L or more in terms of + ) conversion.
  8.  固形分の含有量は20%以上である、請求項1~7のいずれか1項に記載のめっき鋼板の端面防錆処理液。 The end face rustproofing solution for a plated steel sheet according to any one of claims 1 to 7, wherein the solid content is 20% or more.
  9.  pHは7.0以上9.5以下である、請求項1~8のいずれか1項に記載のめっき鋼板の端面防錆処理液。 The end face rustproofing solution for a plated steel sheet according to any one of claims 1 to 8, wherein the pH is 7.0 or more and 9.5 or less.
  10.  めっき鋼板の端面に、請求項1~9のいずれか1項に記載の端面防錆処理液を付与する工程を含む、
     めっき鋼板の端面の化成処理方法。
    A step of applying the end face antirust treatment liquid according to any one of claims 1 to 9 to the end face of the plated steel sheet
    Chemical conversion treatment method of end face of plated steel sheet.
  11.  前記端面防錆処理液は、めっき鋼板の端面の、基材鋼板が露出した部位に付与される、請求項10に記載のめっき鋼板の端面の化成処理方法。 The method for chemical conversion treatment of an end face of a plated steel plate according to claim 10, wherein the end face antirust treatment liquid is applied to a portion of the end face of the plated steel plate where the base steel plate is exposed.
  12.  めっき鋼板と、
     前記めっき鋼板の端面に形成された化成処理皮膜と、を有する化成処理鋼板であって、
     前記化成処理皮膜は、
     フッ素樹脂を含む有機樹脂と、
     第4族元素を含む化合物または第4族元素のイオンと、
     アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、
     シランカップリング剤と、
     を含む、化成処理鋼板。
    Plated steel plate,
    It is a chemical conversion treatment steel plate which has the chemical conversion treatment film formed in the end face of the above-mentioned plating steel plate,
    The chemical conversion film is
    An organic resin containing a fluorine resin,
    A compound containing a Group 4 element or an ion of a Group 4 element;
    An ester compound of adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms, and at least one bond promoter selected from the group consisting of n-methyl-2-pyrrolidone,
    With a silane coupling agent,
    Containing chemically treated steel sheet.
  13.  前記化成処理皮膜は、めっき鋼板の端面の、基材鋼板が露出した部位を被覆するように形成された、請求項12に記載の化成処理鋼板。 The chemical conversion treatment steel plate according to claim 12, wherein the chemical conversion treatment film is formed to cover a portion of the end surface of the plated steel plate where the base steel plate is exposed.
  14.  めっき鋼板の成形加工によって作製された成形加工品であって、
     前記成形加工品は前記めっき鋼板の端面に形成された化成処理皮膜を含み、
     前記化成処理皮膜は、
     フッ素樹脂を含む有機樹脂と、
     第4族元素を含む化合物または第4族元素のイオンと、
     アジピン酸またはフタル酸と炭素数1以上3以下のアルコールとのエステル化合物、およびn-メチル-2-ピロリドンからなる群から選択される1以上の結合促進剤と、
     シランカップリング剤と、
     を含む、成形加工品。
     
    It is a formed product manufactured by forming a plated steel sheet, and
    The molded product includes a chemical conversion coating formed on the end face of the plated steel sheet,
    The chemical conversion film is
    An organic resin containing a fluorine resin,
    A compound containing a Group 4 element or an ion of a Group 4 element;
    An ester compound of adipic acid or phthalic acid and an alcohol having 1 to 3 carbon atoms, and at least one bond promoter selected from the group consisting of n-methyl-2-pyrrolidone,
    With a silane coupling agent,
    Molded and processed products.
PCT/JP2019/001820 2018-01-24 2019-01-22 Anti-rust treatment solution for end face of plated steel sheet, method for chemical conversion treatment of end face of plated steel sheet, chemical conversion treated steel sheet, and molded article WO2019146583A1 (en)

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