EP2081695A1 - Processus pour la production de revêtements multicouches - Google Patents

Processus pour la production de revêtements multicouches

Info

Publication number
EP2081695A1
EP2081695A1 EP07838833A EP07838833A EP2081695A1 EP 2081695 A1 EP2081695 A1 EP 2081695A1 EP 07838833 A EP07838833 A EP 07838833A EP 07838833 A EP07838833 A EP 07838833A EP 2081695 A1 EP2081695 A1 EP 2081695A1
Authority
EP
European Patent Office
Prior art keywords
base coat
borne base
unmodified water
water
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP07838833A
Other languages
German (de)
English (en)
Other versions
EP2081695B1 (fr
Inventor
Frank-Peter Tiegs
Michael Georgiadis
Marc Chilla
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Coatings Foreign IP Co LLC
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of EP2081695A1 publication Critical patent/EP2081695A1/fr
Application granted granted Critical
Publication of EP2081695B1 publication Critical patent/EP2081695B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50—Multilayers
    • B05D7/56—Three layers or more
    • B05D7/57—Three layers or more the last layer being a clear coat

Definitions

  • the invention relates to a process for the production of multi-layer coatings.
  • Automotive coatings generally comprise a separately baked electrodeposition coating (EDC) primer, a separately baked primer surfacer layer (filler layer) applied thereto and a top coat applied thereto comprising a wet-on-wet applied color- and/or special effect-imparting base coat layer and a protective, gloss-imparting clear coat layer.
  • EDC electrodeposition coating
  • the total primer surfacer plus base coat layer thickness is generally 30 to 60 ⁇ m, in case of metallic color shades (color tones) more in the lower range of 30 to 45 ⁇ m.
  • WO 97/47401 and U.S. 5,976,343 for the production of decorative multi-layer coatings, which processes allow for the elimination of the application and separate baking of a primer surfacer layer which, of course, reduces coating material consumption and total layer thickness.
  • a multi-layer coating structure comprising a first, modified water-borne base coat, a second, unmodified water-borne base coat and a clear coat is applied by a wet-on-wet-on-wet process comprising the joint curing of these three coating layers that are applied to a baked EDC primer.
  • these processes use two base coat layers that allow for markedly lower total layer thickness by approximately 15 to 25 ⁇ m, than that of a conventional primer surfacer and base coat.
  • the modified water-borne base coat is produced in these processes from an unmodified water-borne base coat by mixing with an admixture component.
  • the modified water-borne base coat replaces a conventional primer surfacer.
  • WO 97/47401 recommends as an admixture component, the addition of polyisocyanate crosslinking agent, while U.S. 5,976,343 describes the addition of pdlyurethane resin.
  • Bake-cured EDC primer coatings in particular are examples of problematic substrates which are nonuniform in color shade, because they often suffer from severe local discoloration as the result of localized differences in object temperature during bake curing.
  • the problematic color shades are to be found both among solid color shades (plain color shades, single-tone color shades; generally independent of observation angle; pigment content without special effect pigments) and special effect color shades.
  • the problem could be solved by applying the modified and/or the unmodified water-borne base coat in an overall higher, opaque layer thickness.
  • Raising the pigment content of the unmodified water-borne base coat is limited, on the one hand, by the critical pigment volume concentration, but is in general also not feasible with regard to the required technological properties of the finished coating.
  • the invention is directed to a process for the production of multi- layer coatings in A' color shades, comprising the successive steps:
  • the base coat layer is applied in a first layer and in a second layer;
  • the first layer comprises a modified water-borne base coat modAB produced by mixing an unmodified water-borne base coat AB with a pigment-free admixture component and
  • the second layer comprises an unmodified water-borne base coat A having a color shade A', wherein the unmodified water-borne base coat A has a black/white opacity (black/white hiding power) of >25 ⁇ m, wherein the unmodified water-borne base coat AB is a mixture of 100 pbv (parts by volume) of the unmodified water-borne base coat A and
  • the pigment-free admixture component is selected from the group consisting of a pigment-free admixture component I and a pigment- free admixture component II, wherein admixture component I comprises one or more binders C, and being mixed into the unmodified water-borne base coat AB in a ratio by weight of 0.1 to 1 parts of binder(s) C : 1 part of resin solids of the unmodified water-borne base coat AB; and wherein admixture component Il comprises one or more polyisocyanates, and being mixed into the unmodified water-borne base coat AB in a ratio by weight of 0.2 to 1 parts of polyisocyanate : 1 part of resin solids of the unmodified water-borne base coat AB, and wherein the pigment content of the unmodified water-borne base coat B is made such that the multi-layer coating achieved after step
  • film thicknesses indicated in the description and in the claims for coating layers refer in each case to dry film thicknesses.
  • process film thickness is used. The meaning of this term will be explained hereinbelow.
  • black/white opacity is used in the description and the claims. It refers to the dry coating thickness of a coating composition wherein the contrast between the black and white fields of a black and white chart coated with the coating composition is no longer visually discernible (mean coating thickness value determined on the basis of evaluation by 5 independent individuals).
  • the coating composition of which the black/white opacity is to be investigated may be applied in a wedge shape onto a black and white chart and dried or hardened.
  • the term "pigment content” used in the description and in the claims means the sum of all the pigments contained in a coating composition without fillers (extenders).
  • the term “pigments” is used here as in DIN 55944 and covers, in addition to special effect pigments, inorganic white, colored and black pigments and organic colored and black pigments. At the same time, therefore, DIN 55944 distinguishes between pigments and fillers.
  • binders C This serves to distinguish between the binder(s) of the unmodified water- borne base coats A, B and AB and the binder(s) C of the pigment-free admixture component I.
  • delta E values of ⁇ 0.4 determined at an illumination angle of 45° to the perpendicular and an observation angle of 45° relative to the specular reflection are sufficiently small and thus represent color shade consistency in the above sense.
  • delta E values are sufficiently small if the delta E values, when determined at an illumination angle of 45° to the perpendicular and at observation angles of 15, 25, 45, 75 and 110° relative to the specular reflection are in each case ⁇ 2.
  • the reflectance curves of visible light in the range from, for example, 380 to 800 nm of a coated surface are determined at one or more different observation angles.
  • the reflectance curves may, for example, be determined at 5 observation angles, for example at 15, 25, 45, 75 and 110° relative to the specular reflection.
  • the reflectance curves may be used as the basis for calculating the conventional CIELab system colohmetric parameters L * (lightness), a * (red-green value), b * (yellow-blue value) and further also C * (chroma) and h * (hue) (c.f. DIN 6174) or these values are directly output from the measuring instrument.
  • the reflectance curves may be determined using any conventional colorimeters known to the person skilled in the art, for example, the X-Rite MA 68 Il instrument sold by the company X-Rite.
  • step 1 the substrates having an EDC primer are provided, with a base coat layer in a total process film thickness in the range from 10 to 35 ⁇ m.
  • This base coat layer is applied in two layers, i.e., a first layer having an individual process film thickness in the range from, for example, 5 to 25 ⁇ m of a modified water- borne base coat modAB produced by mixing an unmodified water-borne base coat AB with a pigment-free admixture component is applied and a subsequent second layer in an individual process film thickness below black/white opacity, for example, in the range from 3 to 20 ⁇ m of the unmodified water-borne base coat A then is applied.
  • the total process film thickness of the base coat layer is dependent inter alia on color shade.
  • Car manufacturers' requirements for base coat film thickness are expressed in the so-called process film thickness (average film thickness which is desired over the entire body in the automotive original coating process), which depends on the individual color shade, on technological properties to be achieved (e.g., stone chip resistance) and on an economic application of the relevant water-borne base coat, i.e., in as thin a film as possible.
  • the total base coat process film thickness lies in the range from 10 to 35 ⁇ m and is the sum of, for example, 5 to 25 ⁇ m of the modified water-borne base coat modAB plus, for example, 3 to 20 ⁇ m of the unmodified water-borne base coat A.
  • Such film thicknesses for base coats meet the requirements for coating the relevant substrates, for example, automotive bodies.
  • Said specific total process film thickness is here composed of the sum of the specific individual process film thickness, lying within the range of, for example, 5 to 25 ⁇ m, of the corresponding modified water-borne base coat modAB and the specific individual process film thickness, lying within the range of, for example, 3 to 20 ⁇ m of the corresponding unmodified water-borne base coat A.
  • unmodified water-borne base coats A, B and AB are water-borne base coats with problematic color shades and having low hiding power
  • the unmodified water-borne base coats B are water-borne base coats with unproblematic color shades and having sufficient hiding power.
  • the color shades of a coating applied from an unmodified water- borne base coat A in opaque film thickness and of a corresponding multilayer coating prepared according to the process of the invention are so close to each other that an observer virtually cannot perceive a difference between the color shades.
  • the color shades of the unmodified water-borne base coats A and of coatings applied thereof in opaque film thickness are called color shades A'.
  • the color shades of the corresponding multi-layer coatings prepared according to the process of the invention are also called color shades A'.
  • the color shades of the unmodified water-borne base coats B and of coatings applied thereof in opaque film thickness are called color shades B'.
  • the unmodified water-borne base coats AB may be produced by mixing 100 pbv of unmodified water-borne base coat A with 1 to 400 pbv, for example, 1 to 50 pbv of an unmodified water-borne base coat B.
  • the unmodified water-borne base coat B to be mixed with the unmodified water-borne base coat A may be one individual water-borne base coat B or a mixture of two or more different unmodified water-borne base coats B; preferably it is one individual water-borne base coat B.
  • the mixing ratio will be 100 pbv of unmodified water-borne base coat A : 1 to 50 pbv of unmodified water-borne base coat B.
  • a mixing ratio of 100 pbv of unmodified water-borne base coat A : more than 50 to 400 pbv of unmodified water-borne base coat B applies in particular in case the unmodified water-borne base coat B is a light-colored or even a white unmodified water-borne base coat.
  • the modified water-borne base coats modAB may be produced by
  • a modified water-borne base coat modAB produced by mixing an unmodified water-borne base coat AB with a pigment-free admixture component shall not be understood to rule out another mixing sequence.
  • the unmodified water-borne base coats A and B must be chemically compatible with each other, i.e. miscible with each other without problems, for example, without formation of coagulate or precipitate. Whereas this is generally guaranteed in case unmodified water-borne base coats A and B are supplied by the same paint manufacturer, it is necessary to ensure such compatibility in case there is more than one supplier for the unmodified water-borne base coats A and B.
  • the unmodified water-borne base coats A and B to be mixed should not differ from each other too much in viscosity to allow for easy mixing. For example, the difference in viscosity should not exceed 50 mPa-s at a shear rate of 1000 s "1 at 20 0 C.
  • the unmodified water-borne base coats A, B and AB are aqueous coating compositions having a ratio by weight of pigment content to resin solids content of, for example, 0.05 : 1 to 1 : 1.
  • pigment(s), a resin solids content which comprises binder(s), optionally, paste resin(s) and optionally, cross-linking agent(s), optionally, filler(s) and optionally, organic solvent(s)
  • the unmodified water-borne base coats A, B and AB contain in general also conventional additive(s).
  • the unmodified water-borne base coats A, B and AB contain ionically and/or non-ionically stabilized binder systems.
  • anionic stabilization is preferred.
  • Anionic stabilization is preferably achieved by at least partially neutralized carboxyl groups in the binder, while non-ionic stabilization is preferably achieved by lateral or terminal polyethylene oxide units in the binder.
  • the unmodified water- borne base coats A, B and AB may be physically drying or crosslinkable by formation of covalent bonds.
  • the crosslinkable unmodified water-borne base coats A, B and AB forming covalent bonds may be self- or externally crosslinkable systems.
  • the unmodified water-borne base coats A, B and AB contain one or more conventional film-forming binders. They may optionally also contain crosslinking agents if the binders are not self-crosslinkable or physically drying.
  • film-forming binders which may be used, are conventional polyester, polyurethane, (meth)acrylic copolymer and/or hybrid resins derived from these classes of resin. Selection of the optionally contained crosslinking agents depends, in a manner familiar to the person skilled in the art, on the functionality of the binders, i.e., the crosslinking agents are selected in such a way that they exhibit a reactive functionality complementary to the functionality of the binders.
  • binder and crosslinking agent examples include carboxyl/epoxy, hydroxyl/methylol ether and/or methylol (methylol ether and/or methylol preferably, as crosslinkable groups of aminoplast resins, in particular, melamine resins).
  • polyurethane resin does not rule out that the polyurethane resin in question may also contain groups other than urethane groups in the polymer backbone, such as, in particular, ester groups and/or urea groups. Instead, the term
  • polyurethane resin of course, also in particular, includes polyurethane resins which contain polyester polyol building blocks and/or urea groups, wherein the latter may, for example, be formed by the reaction of isocyanate groups with water and/or polyamine. If the process according to the invention is performed with a pigment-free admixture component II, it is preferred to work with unmodified water-borne base coats AB which comprise a resin solids content comprising one or more hydroxyl-functional binders.
  • the hydroxyl value of the resin solids content of the unmodified water-borne base coat AB is, for example, in the range of from 10 to 150 mg KOH/g
  • the NCO/OH molar ratio in the modified water-borne base coat imodAB is, for example, 0.5 : 1 to 25 : 1.
  • higher NCO/OH molar ratios may also arise in the corresponding modified water-borne base coats modAB.
  • the NCO/OH molar ratios may even extend towards infinity.
  • the polyisocyanate in the modified water-borne base coat modAB is consumed by reaction with other constituents, which are reactive in relation to isocyanate groups, for example, with water, hydroxyl-functional solvents and/or with functional groups of binders which are reactive with isocyanate and are different from hydroxyl groups.
  • the unmodified water-borne base coats A, B and AB contain conventional pigments, for example, special effect pigments and/or pigments selected from among white, colored and black pigments.
  • special effect pigments are conventional pigments which impart to a coating color flop and/or lightness flop dependent on the observation angle, such as, non-leafing metal pigments, for example, of aluminum, copper or other metals, interference pigments, such as, for example, metal oxide-coated metal pigments, for example, iron oxide- coated aluminum, coated mica, such as, for example, titanium dioxide- coated mica, graphite effect-imparting pigments, iron oxide in flake form, liquid crystal pigments, coated aluminum oxide pigments, coated silicon dioxide pigments.
  • white, colored and black pigments are the conventional inorganic or organic pigments known to the person skilled in the art, such as, for example, titanium dioxide, iron oxide pigments, carbon black, azo pigments, phthalocyanine pigments, quinacridone pigments, pyrrolopyrrole pigments, perylene pigments.
  • the unmodified water-borne base coats A, B and AB may also contain fillers, for example, in proportions of 0 to 30 wt.% relative to the resin solids content.
  • the fillers do not constitute part of the pigment content of the unmodified water-borne base coats A, B and AB. Examples are barium sulfate, kaolin, talcum, silicon dioxide, layered silicates and any mixtures thereof.
  • the special effect pigments are generally initially introduced in the form of a conventional commercial aqueous or non-aqueous paste, optionally, combined with preferably water-dilutable organic solvents and additives and then mixed with aqueous binder. Pulverulent special-effect pigments may first be processed with preferably water-dilutable organic solvents and additives to yield a paste.
  • White, colored and black pigments and/or fillers may, for example, be ground in a proportion of the aqueous binder. Grinding may preferably also take place in a special aqueous paste resin. Grinding may be performed in conventional assemblies known to the person skilled in the art. The formulation is then completed with the remaining proportion of the aqueous binder or of the aqueous paste resin.
  • the unmodified water-borne base coats A, B and AB may contain conventional additives in conventional quantities, for example, of 0.1 to 5 wt.%, relative to the solids content thereof. Examples are antifoaming agents, wetting agents, adhesion promoters, catalysts, levelling agents, anticratering agents, thickeners and light stabilizers.
  • the water content of the unmodified water-borne base coats A, B and AB is, for example, 60 to 90 wt.%.
  • the unmodified water-borne base coats A, B and AB may contain conventional organic solvents, for example, in a proportion of preferably less than 20 wt.%, particularly preferably, less than 15 wt.%.
  • solvents are mono- or polyhydric alcohols, for example, propanol, butanol, hexanol; glycol ethers or esters, for example, diethylene glycol di- C1 -C6-alkyl ether, dipropylene glycol di-C1 -C6-alkyl ether, ethoxypropanol, ethylene glycol monobutyl ether; glycols, for example, ethylene glycol and/or propylene glycol, and the di- or trimers thereof; N- alkylpyrrolidone, such as, for example, N-methylpyrrolidone; ketones, such as, methyl ethyl ketone, acetone, cyclohexanone; aromatic or aliphatic hydrocarbons, for example, toluene, xylene or linear or branched aliphatic C6-C12 hydrocarbons.
  • glycol ethers or esters for example, diethylene glycol di- C1 -C
  • the unmodified water-borne base coats A, B and AB have solids contents of, for example, 10 to 40 wt.%, preferably, of 15 to 30 wt.%.
  • the unmodified water-borne base coats A have a black/white opacity of >25 ⁇ m, i.e. they are water-borne base coats with problematic color shades and having low hiding power. They comprise pigments which according to the kind and/or quantity thereof allow only for a low hiding power. Examples are in particular unmodified water-borne base coats A with certain, in particular luminous blue, red, yellow or orange color shades which are especially distinguished by elevated brilliance and color purity. They may comprise solid color shades or special effect color shades, such as mica or metallic color shades.
  • the unmodified water-borne base coats A in particular comprise those which, despite their black/white opacity of >25 ⁇ m, are non-critical with regard to UV transmission, i.e., they comprise water-borne base coats which are distinguished in that UV light corresponding to a UV transmission of less than 0.1% in the wavelength range of from 280 to 380 nm, of less than 0.5% in the wavelength range of from 380 to 400 nm and of less than 1 % in the wavelength range of from 400 to 450 nm may penetrate through a base coat layer applied in the process film thickness and (i) consisting of a relevant unmodified water-borne base coat A mixed with the pigment-free admixture component I in a ratio by weight of 0.1 to 1 parts of binder(s) C : 1 part of resin solids of the unmodified water-borne base coat A and the corresponding unmodified water-borne base coat A or (ii) consisting of a relevant unmodified water-borne base coat A mixed with the pigment-free admi
  • those unmodified water-borne base coats A have levels of pigmentation (ratio by weight of pigment content to resin solids content) and/or such pigment contents that, by virtue of the type and proportion of the constituent pigments, UV light corresponding to a UV transmission of less than 0.1% in the wavelength range of from 280 to 380 nm, of less than 0.5% in the wavelength range of from 380 to 400 nm and of less than 1% in the wavelength range of from 400 to 450 nm may penetrate through a base coat layer applied in the process film thickness and (i) consisting of a relevant unmodified water-borne base coat A mixed with the pigment-free admixture component I in a ratio by weight of 0.1 to 1 parts of binder(s) C : 1 part of resin solids of the unmodified water-borne base coat A and the corresponding unmodified water-borne base coat A or (ii) consisting of a relevant unmodified water-borne base coat A mixed with the pigment-free admixture component Il in a ratio by weight
  • those unmodified water- borne base coats A have levels of pigmentation and/or pigment contents with or with sufficient proportions of pigments which effectively reduce UV transmission.
  • UV transmission may be measured by applying a corresponding coating structure of unmodified water-borne base coat A mixed with the pigment-free admixture component I or Il and unmodified water-borne base coat A to a UV light-transmitting support, for example, a silica glass plate, and measuring the UV transmission in the corresponding wavelength range using a corresponding uncoated UV light-transmitting support as reference.
  • the unmodified water-borne base coats B are water-borne base coats with unproblematic color shades and having sufficient hiding power, i.e.
  • the pigment content of the unmodified water-borne base coat B is made such that, with a given (particular) unmodified water-borne base coat A, a given specific total process film thickness (and in each case also specific individual process film thicknesses for the modified water-borne base coat modAB and for the unmodified water-borne base coat A), a given mixing ratio of unmodified water-borne base coat A and B in the corresponding aforementioned range, a given mixing ratio of pigment-free admixture component I or Il and unmodified water-borne base coat AB in the corresponding aforementioned range, the multi-layer coating produced from the modified water-borne base coat modAB applied to at least 80% of the specific individual process film thickness, from the corresponding unmodified water-borne base coat A applied to at least 80% of the specific individual process film thickness and the clear coat achieves color shade consistency.
  • the pigment content of the unmodified water- borne base coat B is selected by type (qualitative and quantitative composition of the pigments forming the pigment content) and quantity accordingly.
  • the pigment contents of unmodified water-borne base coats B in particular comprise hiding power imparting pigments. Pigments capable of providing hiding power are known to the skilled person developing color shades of coatings. Suitable pigment contents are, for example, those with elevated proportions of hiding power imparting pigments within the pigment composition, for example, with 30 or more wt.% of carbon black, 70 or more wt.% of titanium dioxide or 40 or more wt.% of phthalocyanine pigments.
  • the modified water-borne base coat modAB is produced from the unmodified water-borne base coat AB by mixing with the pigment-free admixture component I in a ratio by weight of 0.1 to 1 parts, preferably of 0.1 to 0.5 parts of binder(s) C : 1 part of resin solids of the unmodified water-borne base coat AB.
  • the addition of the pigment-free admixture component I to the unmodified water-borne base coat AB imparts to the resultant modified water-borne base coat modAB technological properties, such as, for example, stone chip resistance, which are important to the finished multilayer coating. It is moreover ensured in this manner that color-consistent multi-layer coatings in the desired color shade (color shade specified by a coated standard) are obtained.
  • the pigment-free admixture component I containing one or more binder(s) C is a composition with a solids content of, for example, 20 to 95 wt.%, in general, of 30 to 60 wt.%.
  • the volatile content is formed, in addition to possible volatile additives, by water and/or organic solvent.
  • the solids content itself consists of the resin solids content plus possible nonvolatile additives.
  • the resin solids content of the pigment-free admixture component I comprises one or more binders C and, optionally, one or more crosslinking agents, for example, blocked polyisocyanates, aminoplast resins, such as, for example, melamine resins.
  • the resin solids content consists to an extent of, for example, 70 to 100 wt.% of the at least one binder C plus 0 to 30 wt.% of at least one crosslinking agent, wherein the weight percentages add up to 100 wt.%.
  • the binder(s) C of the pigment-free admixture component I may comprise the same binders as in the unmodified water-borne base coats A, B or AB and/or binders which differ therefrom.
  • the binder(s) C are conventional water-dilutable, preferably anionically stabilized binders, for example, corresponding polyester, polyurethane, (meth)acrylic copolymer and/or hybrid resins derived from these classes of resin. Polyester and in particular polyurethane resins are preferred.
  • the binders C may comprise functional groups which may be involved in a crosslinking reaction which optionally proceeds during the subsequent thermal curing of the modified water-borne base coat modAB; such crosslinking reactions are in particular addition and/or condensation reactions.
  • the binders C may also be self-crosslinkable. Examples of binders' C functional groups are hydroxyl groups, blocked isocyanate groups and epoxy groups.
  • the pigment-free admixture component I generally comprises an aqueous composition; it then contains, for example, 20 to 70 wt.% water. Irrespective of whether it is an aqueous or non-aqueous composition, the pigment-free admixture component I may contain one or more organic solvents, for example, in a total quantity of 5 to 70 wt.%.
  • solvents are mono- or polyhydric alcohols, for example, propanol, butanol, hexanol; glycol ethers or esters, for example, diethylene glycol C1-C6 dialkyl ethers, dipropylene glycol C1-C6 dialkyl ethers, ethoxypropanol, butylglycol; glycols, for example, ethylene glycol and/or propylene glycol, and the di- or trimers thereof; N-alkylpyrrolidones, for example N-methylpyrrolidone and ketones, for example, methyl ethyl ketone, acetone, cyclohexanone; aromatic or aliphatic hydrocarbons, for example, toluene, xylene, or linear or branched aliphatic C6-C12 hydrocarbons.
  • glycol ethers or esters for example, diethylene glycol C1-C6 dialkyl ethers, dipropylene glycol C
  • the solvents are preferably water-dilutable.
  • the pigment-free admixture component I may contain additives in proportions of in each case, for example, 0.1 to 4 wt.%, corresponding to a total quantity of in general no more than 6 wt.%.
  • additives are defoamers, anticratehng agents, wetting agents, neutralizing agents, light stabilizers and rheology control agents.
  • the modified water-borne base coat modAB is produced from the unmodified water-borne base coat AB by mixing with the pigment-free admixture component Il in a ratio by weight of 0.2 to 1 parts, preferably of 0.2 to 0.8 parts of polyisocyanate : 1 part of resin solids of the unmodified water-borne base coat AB.
  • the addition of the pigment-free admixture component Il to the unmodified water-borne base coat AB imparts to the resultant modified water-borne base coat technological properties, such as, for example, stone chip resistance, which are important to the finished multi-layer coating. It is moreover ensured in this manner that color-consistent multilayer coatings in the desired color shade (color shade specified by a coated standard) are obtained.
  • the pigment-free admixture component Il containing one or more polyisocyanates is a composition with a solids content of, for example, 20 to 95 wt.%, in general, of 40 to 80 wt.%.
  • the volatile content is formed, in addition to possible volatile additives, by water and/or organic solvent.
  • the solids content itself consists of the resin solids content and, optionally, plus nonvolatile additives.
  • the resin solids content of the pigment-free admixture component Il comprises one or more polyisocyanates.
  • the resin solids content consists to an extent of 100 wt.% of polyisocyanate(s).
  • polyisocyanate(s) used in connection with the pigment- free admixture component Il is not restricted to the meaning free polyisocyanate or free polyisocyanates, but instead also includes blocked polyisocyanate or blocked polyisocyanates.
  • the polyisocyanates comprise di- and/or poly-isocyanates with aliphatically, cycloaliphatically, araliphatically and/or less preferably aromatically attached isocyanate groups.
  • the polyisocyanates are liquid at room temperature or are present as an organic solution; the polyisocyanates here exhibit at 23°C a viscosity of in general 0.5 to 2000 mPa-s.
  • the isocyanate content of the polyisocyanates present in the form of free or latent (blocked, thermally re- dissociable) isocyanate groups is in general in a range from 2 to 25 wt.%, preferably, from 5 to 25 wt.% (calculated as NCO).
  • diisocyanates examples include hexamethylene diisocyanate, tetramethylxylylene diisocyanate, isophorone diisocyanate, dicyclohexylmethane diisocyanate, and cyclohexane diisocyanate.
  • polyisocyanates are those which contain heteroatoms in the residue linking the isocyanate groups. Examples of these are polyisocyanates which contain carbodiimide groups, allophanate groups, isocyanurate groups, uretidione groups, urethane groups, acylated urea groups or biuret groups.
  • the polyisocyanates preferably have an isocyanate functionality higher than 2, such as, for example, polyisocyanates of the uretidione or isocyanurate type produced by di- or trimerization of the above-mentioned diisocyanates.
  • Further examples are polyisocyanates produced by reaction of the above-mentioned diisocyanates with water and containing biuret groups or polyisocyanates produced by reaction with polyols and containing urethane groups.
  • coating polyisocyanates based on hexamethylene diisocyanate, isophorone diisocyanate or dicyclohexylmethane diisocyanate.
  • Coating polyisocyanates based on these diisocyanates means the per se known biuret, urethane, uretidione and/or isocyanurate group-containing derivatives of these diisocyanates.
  • the polyisocyanates may be used in blocked form, though this is not preferred. They may be blocked with conventional blocking agents that can be de-blocked under the action of heat, for example, with alcohols, oximes, amines and/or CH-acidic compounds.
  • the blocked or preferably free polyisocyanates may be used in the pigment-free admixture component Il as such or as a preparation containing water and/or organic solvent, wherein in the case of free polyisocyanate no water and no organic solvent with active hydrogen is used. It may be desirable, for example, for the polyisocyanates to be pre- diluted with a water-miscible organic solvent or solvent mixture. In this case, it is preferable to use solvents, which are inert relative to isocyanate groups, especially where the preferred free polyisocyanates are used.
  • solvents which do not contain any active hydrogen for example, ethers, such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether; glycol ether esters, such as, ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, methoxypropyl acetate; and N-methylpyrrolidone.
  • ethers such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether
  • glycol ether esters such as, ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, methoxypropyl acetate
  • N-methylpyrrolidone for example, ethers, such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether
  • glycol ether esters such as, ethylene glycol monobutyl ether acetate, diethylene glyco
  • hydrophilic polyisocyanates which may be stabilized in the aqueous phase by a sufficient number of ionic groups and/or by terminal or lateral polyether chains.
  • Hydrophilic polyisocyanates are sold as commercial products, for example, by Bayer under the name Bayhydur®.
  • a preferred pigment-free admixture component Il containing free polyisocyanate it is expedient not only to avoid the deliberate addition of water, but also to perform processing with the most extensive possible, preferably complete, exclusion of water and in general also with the most extensive possible, preferably complete, exclusion of other substances reactive towards isocyanate groups, such as, for example, alcohols.
  • water-binding auxiliaries For example, water scavengers, such as, orthoesters may be added during production and storage of the pigment-free admixture component Il containing free polyisocyanate.
  • the pigment-free admixture component Il may, if it contains no free polyisocyanate, contain, for example, 20 to 70 wt.% water.
  • the pigment-free admixture component Il may contain one or more organic solvents, for example, in a total quantity of 5 to 70 wt.%.
  • the solvents are preferably water-dilutable.
  • the solvents are those which are inert towards isocyanate groups.
  • Suitable solvents are ethers, such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether; glycol ether esters, such as, ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, methoxypropyl acetate; and N-methylpyrrolidone.
  • ethers such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether
  • glycol ether esters such as, ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, methoxypropyl acetate
  • N-methylpyrrolidone such as, for example, diethylene glycol diethyl ether, dipropylene glycol dimethyl ether
  • glycol ether esters such as, ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, methoxy
  • the pigment-free admixture component Il may contain additives in proportions of in each case, for example, 0.1 to 2 wt.%, corresponding a total quantity of in general no more than 5 wt.%. Examples of additives are the same as those already mentioned for the pigment-free admixture component I.
  • the substrates are provided with multi-layer coatings in A' color shades.
  • the multi-layer coating process according to the invention is performed in an industrial coating facility, i.e. within a mass-production coating line.
  • the B' color shade program comprises two or more differently colored unmodified water-borne base coats B. This allows for the selection of an appropriate unmodified water-borne base coat B (one individual water-borne base coat B or a mixture of two or more different unmodified water-borne base coats B). In particular such selection may happen dependent on the color shade of the relevant unmodified water-borne base coat A to be mixed with.
  • the unmodified water-borne base coats B comprise unmodified water-borne base coats with unproblematic color shades and having sufficient hiding power. Therefore, the process for the production of multi-layer coatings on substrates in B' color shades is different from the process according to the invention.
  • the process for the production of multi-layer coatings in B' color shades comprises the successive steps:
  • the base coat layer is applied in a first layer and, optionally, in a second layer;
  • the first layer comprises a modified water-borne base coat modB produced by mixing an unmodified water-borne base coat B having a color shade B' with a pigment-free admixture component and the optionally applied second layer comprises the unmodified water-borne base coat B, wherein the pigment-free admixture component is selected from the group consisting of a pigment-free admixture component I and a pigment- free admixture component II, wherein admixture component I comprises one or more binders C, and being mixed into the unmodified water-borne base coat B in a ratio by weight of 0.1 to 1 parts of binder(s) C : 1 part of resin solids of the unmodified water-borne base coat B; and wherein admixture component Il comprises one or more polyisocyanates, and being mixed into the unmodified water
  • the unmodified water- borne base coats A, B and the pigment-free admixture component I or Il are mixed preferably on the user's premises, in particular shortly or immediately before application of the resultant modified water-borne base coat modAB.
  • the mixing sequence there are various possibilities for the mixing sequence.
  • the unmodified water- borne base coats A and B in each case of a different color shade are each conveyed in their own circulating line.
  • the pigment-free admixture component I or Il to be added is preferably used in the form of a single general purpose admixture component, the one pigment-free admixture component I or Il likewise being guided in its own circulating line and automatically mixed with the respective unmodified water-borne base coats A and B using mixing technology conventional in industrial coating facilities, for example, a static mixer like a Kenics mixer.
  • the EDC-primed substrates are initially spray-coated with the modified water-borne base coat modAB, preferably by electrostatically-assisted high-speed rotary atomization.
  • the corresponding unmodified water-borne base coat A is spray-applied, preferably by pneumatic spray application.
  • a brief flash-off phase of, for example, 30 seconds to 10 minutes at an air temperature of 20 to 100 0 C, after which the clear coat is applied in a dry film thickness of, for example, 20 to 60 ⁇ m.
  • All known clear coats are in principle suitable as the clear coat.
  • Usable clear coats are both solvent-containing one-component (1 pack) or two-component (2 pack) clear coats, water-dilutable 1 pack or 2 pack clear coats, powder clear coats or aqueous powder clear coat slurries.
  • the applied water-borne base coat layer consisting of modified water-borne base coat modAB and unmodified water-borne base coat A and the clear coat layer are jointly cured, for example, by baking, for example, at 80 to 160 0 C object temperature. It is advantageous that repair coating of multi-layer coatings produced by the process according to the invention can be carried out with the unmodified water-borne base coat A of the relevant problematic color shade without there being any visually perceptible deviation in color shade in the area of the repair. In other words, consistency in color shade of the kind already mentioned above is ensured, even if the repair coating is performed using only the corresponding unmodified water-borne base coat A and not also the modified water-borne base coat modAB. Examples
  • Example 1 (Production of a white unmodified water-borne base coat):
  • a white unmodified water-borne base coat of the following composition was produced:
  • TiPure® R 706 from DuPont
  • Example 2 (Production of a polvisocvanate admixture component): A mixture of
  • Example 3 (Production of water-borne base coats): a) A yellow unmodified water-borne base coat of the following composition was produced:
  • the yellow unmodified water-borne base coat had a black/white opacity of 52 ⁇ m and a specific individual process film thickness of 15 ⁇ m.
  • a modified water-borne base coat was produced by mixing 100 pbw of the yellow unmodified water-borne base coat from a) with 400 pbw of the white unmodified water-borne base coat from Example 1 and with 50 pbw of the polyisocyanate admixture component from Example 2.
  • the modified water-borne base coat had a specific individual process film thickness of 15 ⁇ m.
  • a water-borne coating composition was produced by mixing 100 pbw of the unmodified water-borne base coat from a) with 10 pbw of the polyisocyanate admixture component from Example 2.
  • a multi-layer coating 4a was obtained by the following procedure:
  • the yellow unmodified water-borne base coat 3a was spray applied in a wedge- shaped gradient (wedge in longitudinal direction) to a dry film thickness range from 0 to 20 ⁇ m and allowed to flash-off for 5 minutes at 80°C.
  • test panels provided in this way with a flashed off base coat layer were then spray coated with a commercial two-component polyurethane clear coat in a dry film thickness of 40 ⁇ m and after flashing- off for 5 minutes at 20 0 C baked for 20 minutes at 140°C object temperature.
  • a multi-layer coating 4b was obtained by repeating Example 4a with the difference that the water-borne coating composition 3c was used instead of water-borne base coat 3b.
  • the yellow unmodified water-borne base coat 3a was spray applied in a dry film thickness of 60 ⁇ m to an automotive steel test panel provided with the dark-grey EDC primer. To this end 3 spray passes in each case followed by a forced drying step of 5 minutes at 7O 0 C were performed.
  • the two-component polyurethane clear coat was spray applied in a dry film thickness of 40 ⁇ m and after flashing- off for 5 minutes at 20°C baked for 20 minutes at 140°C object temperature.
  • the multi-layer coatings 4a and 4b so obtained were in each case colorimetrically assessed at an illumination angle of 45° to the perpendicular and an observation angle of 45° relative to the specular reflection in accordance with the method known from US 5,991 ,042 using the X-Rite MA 68 Il instrument sold by the company X-Rite.
  • Multi-layer coating 4c was colorimetrically measured using the same equipment.
  • Table 1 shows the delta E values calculated from the colorimetric data as a function of the dry film thickness of the unmodified water-borne base coat 3a
  • delta E 4a square root of (L * 4c 2 - L * 4a 2 + c * 4c 2 - c * 4a 2 + h * 4c 2 - h * 4a 2 );
  • delta E 4b square root of (L * 4c 2 - L * 4b 2 + c * 4c 2 - c * 4 b 2 + h * 4c 2 - h * 4b 2 )].

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Paints Or Removers (AREA)

Abstract

Les étapes du processus selon l'invention pour la production de revêtements multicouches en nuances de couleurs A' consistent : 1) à appliquer une couche de revêtement de base d'épaisseur de pellicule de processus totale comprise entre 10 et 35 µm sur un substrat comportant un primaire EDC ; 2) à appliquer une couche de revêtement clair sur la couche de revêtement de base ; 3) à cuire conjointement les couches de revêtement de base et de revêtement clair. La couche de revêtement de base est appliquée en une première couche d'un revêtement aqueux modAB modifié préparé en mélangeant un revêtement de base de base aqueux A non modifié d'opacité noir/blanc >25 µm à un revêtement de base aqueux B non modifié et à un adjuvant non pigmenté et en une seconde couche du revêtement de base aqueux A non modifié.
EP07838833.7A 2006-10-25 2007-09-25 Processus pour la production de revêtements multicouches Active EP2081695B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85426906P 2006-10-25 2006-10-25
PCT/US2007/020704 WO2008051346A1 (fr) 2006-10-25 2007-09-25 Processus pour la production de revêtements multicouches

Publications (2)

Publication Number Publication Date
EP2081695A1 true EP2081695A1 (fr) 2009-07-29
EP2081695B1 EP2081695B1 (fr) 2015-12-02

Family

ID=39133690

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07838833.7A Active EP2081695B1 (fr) 2006-10-25 2007-09-25 Processus pour la production de revêtements multicouches

Country Status (5)

Country Link
EP (1) EP2081695B1 (fr)
JP (1) JP2010507478A (fr)
BR (1) BRPI0716280A2 (fr)
MX (1) MX2009004278A (fr)
WO (1) WO2008051346A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2204239A1 (fr) 2008-12-23 2010-07-07 E. I. du Pont de Nemours and Company Procédé pour la production de revêtements multicouches
JP5227881B2 (ja) * 2009-04-24 2013-07-03 マツダ株式会社 積層塗膜構造
JP5625434B2 (ja) 2010-03-29 2014-11-19 マツダ株式会社 積層塗膜形成方法
US11980912B2 (en) 2018-06-11 2024-05-14 Ppg Industries Ohio, Inc. Multi-layer coatings and methods of preparing the same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060008588A1 (en) * 2004-07-12 2006-01-12 Marc Chilla Process for the production of multi-layer coatings
US20060068116A1 (en) * 2004-09-27 2006-03-30 Marc Chilla Process for the production of multi-layer coatings in light metallic color shades
US20060134334A1 (en) * 2004-12-22 2006-06-22 Marc Chilla Process for the production of primer surfacer-free multi-layer coatings
US20070071901A1 (en) * 2005-09-29 2007-03-29 Giannoula Avgenaki Process for the production of multi-layer coatings
ES2387921T3 (es) * 2006-06-14 2012-10-04 E.I. Du Pont De Nemours And Company Procedimiento para la producción de revestimientos multicapas

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2008051346A1 *

Also Published As

Publication number Publication date
EP2081695B1 (fr) 2015-12-02
WO2008051346A1 (fr) 2008-05-02
BRPI0716280A2 (pt) 2013-12-24
JP2010507478A (ja) 2010-03-11
MX2009004278A (es) 2009-05-05

Similar Documents

Publication Publication Date Title
EP2035154B1 (fr) Procédé de fabrication de revêtements multi-couches
EP1893352B1 (fr) Procede de production de revetements multicouches
EP1937417B1 (fr) Procede de production de revetements multicouche
EP1765523B1 (fr) Procédé de production de revêtements multicouches
EP1843862B1 (fr) Procede d'obtention de revetements multicouches sans appret d'impression
EP1682285B1 (fr) Procede de production de revetements multicouches de teintes metalliques claires
US8877295B2 (en) Process for the production of multi-layer coatings
EP1838459B1 (fr) Procede de production de revetements multicouche depourvus d'appret surfaçant
EP2081695B1 (fr) Processus pour la production de revêtements multicouches
US8147919B2 (en) Process for the production of multi-layer coatings
US8865262B2 (en) Process for producing multi-layer coatings in light metallic color shades
US7968151B2 (en) Process for the production of multi-layer coatings

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20090513

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20100810

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COATINGS FOREIGN IP CO. LLC

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20150624

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 763385

Country of ref document: AT

Kind code of ref document: T

Effective date: 20151215

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602007044114

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20160302

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 763385

Country of ref document: AT

Kind code of ref document: T

Effective date: 20151202

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602007044114

Country of ref document: DE

Representative=s name: LKGLOBAL | LORENZ & KOPF PARTG MBB PATENTANWAE, DE

Ref country code: DE

Ref legal event code: R082

Ref document number: 602007044114

Country of ref document: DE

Representative=s name: KOPF WESTENBERGER WACHENHAUSEN PATENTANWAELTE , DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20160303

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20160402

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20160404

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602007044114

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

26N No opposition filed

Effective date: 20160905

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20160925

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20170531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160925

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160930

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160930

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160930

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160925

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160925

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20070925

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151202

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602007044114

Country of ref document: DE

Owner name: AXALTA COATING SYSTEMS GMBH, CH

Free format text: FORMER OWNER: COATINGS FOREIGN IP CO. LLC, WILMINGTON, DEL., US

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230510

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230927

Year of fee payment: 17