EP0797631A1 - Artificial patina - Google Patents

Artificial patina

Info

Publication number
EP0797631A1
EP0797631A1 EP95916502A EP95916502A EP0797631A1 EP 0797631 A1 EP0797631 A1 EP 0797631A1 EP 95916502 A EP95916502 A EP 95916502A EP 95916502 A EP95916502 A EP 95916502A EP 0797631 A1 EP0797631 A1 EP 0797631A1
Authority
EP
European Patent Office
Prior art keywords
copper
formulation
acid
substrate
patina
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.)
Withdrawn
Application number
EP95916502A
Other languages
German (de)
French (fr)
Other versions
EP0797631A4 (en
Inventor
Andrej Atrens
Jason Nairn
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.)
University of Queensland UQ
Copper Refineries Pty Ltd
Original Assignee
University of Queensland UQ
Copper Refineries Pty Ltd
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 University of Queensland UQ, Copper Refineries Pty Ltd filed Critical University of Queensland UQ
Publication of EP0797631A1 publication Critical patent/EP0797631A1/en
Publication of EP0797631A4 publication Critical patent/EP0797631A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B22/00—Use of inorganic materials as active ingredients for mortars, concrete or artificial stone, e.g. accelerators, shrinkage compensating agents
    • C04B22/08—Acids or salts thereof
    • C04B22/14—Acids or salts thereof containing sulfur in the anion, e.g. sulfides
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/24—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing alkyl, ammonium or metal silicates; containing silica sols
    • C04B28/26—Silicates of the alkali metals
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
    • C—CHEMISTRY; METALLURGY
    • C23—COATING 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
    • C23C—COATING 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
    • C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/40—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00482—Coating or impregnation materials
    • C04B2111/00525—Coating or impregnation materials for metallic surfaces

Definitions

  • This invention relates to an artificial patina for coating copper substrates.
  • a patina When exposed to the atmosphere over time copper substrates develop a stable greenish-blue film known as a patina.
  • the copper which is initially bright orange first forms a uniform thin layer of matt brown cuprite (Cu applying0) which is then, over time, coated by a green-blue patina layer of between 5 to 15 micrometre thickness .
  • the nature of the film varies according to the locality of the substrate.
  • the patina consists mainly of basic copper sulphate (brochantite CuSO..3Cu(OH)neig) and in marine localities, the patina consists mainly of basic copper chloride (atacamite) .
  • At least 4 years, more typically at least 10 years is necessary for the formation of a natural patina coating. In normal city atmospheres a patina will generally form after 8 to 12 years. In urban atmospheres, the time period is 16 to 20 years.
  • U.S. patent No. 3,152,927 discloses a formulation for an artificial patina which can be applied in the manufacturing plant to produce a pre-patinated copper sheet. These sheets can then be installed at the chosen site.
  • the patination process comprises producing a basic copper nitrate sludge (with excess Cu(OH)_) which is then applied to oxidised copper sheets and allowed to dry.
  • the artificial patina coating formed is, however, a basic copper nitrate and is unstable and will undergo competitive reaction to convert the patina to the natural form. This can result in peeling of the applied patina.
  • the Copper and Brass Research Association (“CABRA) ("Artificial Patination” from Copper Roofing CDA Publication No. 57, 1959) developed a spray method for the coating of large copper objects (eg. roofs) .
  • the spray solution comprises ammonium sulphate, copper sulphate, ammonia and water.
  • the solution is sprayed onto the surface and allowed to dry. This is repeated five to six times .
  • the development of colour depends on suitable weather conditions and rain within eight hours can wash away the solution before the reaction has started. Ideal conditions need fog or a relative humidity of at least 80%.
  • the sheets obtained a patina after about 4 days .
  • This patina is chemically identical to a natural patina but has a different microstructural morphology resulting in easy removal of most of the blue coating.
  • the patina is also a bright blue colour and not the natural blue-green.
  • Major difficulties were experienced in semi-commercial scale production due to the changing solution chemistry (eg. chloride content) of the bath resulting in poor control of the process .
  • the pre-patinated sheets performed well when installed on exposure racks or a roof.
  • Kobe Steel Ltd (Japan) (Toso Kogaku (Coatings Technology) volume 24 number 7 pages 271-275, 1989) developed a technology allowing the production of an artificial patina in a continuous fashion.
  • the method involves treating a clean plain copper sheet with a colouring agent based on basic copper chloride (atacamite) .
  • This coloured layer is applied with a roller and an upper layer of water based acrylic emulsion resin is sprayed over the top to ensure adhesion of the colour film. It is believed that this upper layer treatment will disappear with time and that the basic copper chloride coloured layer will react to form the naturally occurring patina.
  • the artificial patina formed has excellent adhesion properties and can withstand severe metalworking (bending, deep drawing) . In addition accelerated corrosion tests and atmospheric exposure tests have indicated that the artificial patina will react to form the naturally occurring compounds.
  • Natural patinas have a blue-green cast and a streaky, mottled appearance.
  • the coating is softer than a natural patina and can be abraded or peeled off due to the continuous acrylic layer.
  • an artificial patination formulation comprising:
  • a method of coating a copper substrate with an artificial patina comprises applying to the substrate a formulation according to the first aspect.
  • a method of coating a copper substrate with an artificial patina comprises contacting the copper substrate with a persulphate solution, and then allowing the contacted surface to oxidize in a high humidity atmosphere.
  • the copper substrate can be any copper or copper alloy.
  • the substrate will typically be in fabricated or sheet form which may or may not have been pickled and/or acid-cleaned.
  • copper sheeting roofing panels manufactured from copper electrosheet are suitable.
  • Copper "electrosheet” is copper cathode prepared by the electrolytic refining of copper anodes .
  • the substrate is oxidized.
  • an aged electrosheet eg. a four week old electrosheet exhibiting a 3 to 6 micrometer oxide film
  • a four week old electrosheet exhibiting a 3 to 6 micrometer oxide film
  • the substrate may be pretreated with an oxidizing procedure.
  • the formulation can be applied to the copper substrate after installation or can be applied before installation as part of an in-line manufacturing process of the substrate.
  • the formulation can be applied by any suitable application process, typically paintbrush, spray process or by rolling.
  • the hydroxide compound is an alkali metal hydroxide such as sodium hydroxide, potassium hydroxide, an alkaline earth metal hydroxide such as barium hydroxide, a transition metal hydroxide or an ammonium hydroxide.
  • the hydroxide is sodium hydroxide.
  • the iron sulphate is added in an amount to provide a patina containing up to 10 wt% iron.
  • the reaction product is formed by dissolving copper sulphate pentahydrate (eg. 500 g) with iron sulphate heptahydrate (eg. 25 g) in water (eg. 4L) , and then adding sodium hydroxide (eg. IM, 40 g/L, 3.132L) preferably quickly so as to form a fine precipitate.
  • the final reaction product has a composition:
  • a suitable binder includes inorganic silicates preferably water-borne, inorganic silicates such as
  • ZincanodeTM 215 available from ICI-Dulux.
  • ZincanodeTM 215 is a high ratio, high build water-borne self curing inorganic silicate.
  • lOOg to l,000g of the reaction product is used per 1 litre of binder, more preferably 350g to 450g per litre.
  • the formulation may further comprise a carboxylic acid.
  • Suitable carboxylic acids include oxalic acid, capric acid, citric acid, tartic acid, D.L. malic acid, sebacic acid, benzoic acid, succinic acid and stearic acid.
  • the carboxylic acid is present in an amount from 0 to 1000 ppm based on the total weight of the formulation.
  • a patina can also be formed by contacting the copper substrate with a strong oxidant such as a persulphate solution.
  • a strong oxidant such as a persulphate solution.
  • the solution of persulphate is a solution of sodium or ammonium persulphate (typically containing between 10 and 200 g/L in the pH range 3 to 8) .
  • the copper substrate can be contacted by spraying the solution onto the substrate.
  • the contacted surface is then allowed to oxidise in high humidity, typically 95% relative humidity by placing the substrate into a humidity cabinet or conducting the process in a natural high humidity environment.
  • An artificial patina on the substrate results.
  • the substrate can then be washed to remove any residual sodium sulphate.
  • EXAMPLE 1 Dissolve 500g CuSO 4 .5H 2 0 and 25g FeSO .7H_0 in 4 litres of water. Add 3.1 litres of IM NaOH (40g/litre) solution. Wash and dry precipitate to produce a "dry" powder. Add 350g of powder to 1 litre of water borne inorganic silicate (Zincanode 215), mix and apply to copper surface.
  • EXAMPLE 2 Dissolve 500g CuS0..5H 2 0 and 5g FeS0..7H 2 0 in 4 litres of water. Add 2.9 litres of IM NaOH (40g/litre) solution. Wash and dry precipitate to produce a "dry" powder. Add 650g of powder to 1 litre of water borne inorganic silicate (Zincanode 215), mix and apply to copper surface.
  • EXAMPLE 3 Dissolve 500g CuSO..H 2 0 and 15g FeS0..7H 2 0 in 4 litres of water. Add 3.0 litres of IM KOH solution. Wash and dry precipitate to produce a "dry" powder. Add 450g of powder and lOOmg oxalic acid to 1 litre of water borne inorganic silicate (Zincanode 215) , mix and apply to copper surface.
  • the processes and formulations of the present invention are suitable for forming a patina on any copper substrate.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

The invention relates to an artificial patination formulation and method of coating a copper substrate with an artificial patina. The formulation comprises the reaction product of copper sulfate and optionally iron sulphate, with an inorganic hydroxide compound; and a suitable binder. The invention also relates to a method of coating a copper substrate with an artificial patina comprising contacting the copper substrate with a persulphate solution and then allowing the contacted surface to oxidize in a high humidity atmosphere.

Description

Title: ARTIFICIAL PATINA
FIELD OF THE INVENTION
This invention relates to an artificial patina for coating copper substrates.
BACKGROUND OF THE INVENTION
When exposed to the atmosphere over time copper substrates develop a stable greenish-blue film known as a patina. Typically, the copper, which is initially bright orange first forms a uniform thin layer of matt brown cuprite (Cu„0) which is then, over time, coated by a green-blue patina layer of between 5 to 15 micrometre thickness . The nature of the film varies according to the locality of the substrate. Generally, in industrial and urban localities, the patina consists mainly of basic copper sulphate (brochantite CuSO..3Cu(OH) „) and in marine localities, the patina consists mainly of basic copper chloride (atacamite) . At least 4 years, more typically at least 10 years is necessary for the formation of a natural patina coating. In normal city atmospheres a patina will generally form after 8 to 12 years. In urban atmospheres, the time period is 16 to 20 years.
It is generally regarded that copper substrates coated with a patina are aesthetically pleasing and much use of copper is based on the knowledge that a patina will form. Because of the long period of time required to naturally form a patina, it would be desirable to develop a process and formulation which is capable of forming a patina coating on a copper substrate in a much shorter time.
Hitherto, a number of attempts have been made to develop an artificial patination formulation capable of forming a patina in a short amount of time. Broadly, these previous formulations can be divided into two groups:
(i) formulations which are applied to the copper substrate as a solution or paste that react with the copper metal to form a patina,- and
(ii) formulations which contain a pigment that is applied like a paint and bonds to the copper substrate.
Previous formulations, however, suffer from the disadvantage that none have been capable of producing an artificial patina which matches natural patina in composition and which is stable upon exposure to the atmosphere. The majority of previous artificial patinas peel off after a short time due to poor adhesion of the patina to the metal substrate and special conditions are sometimes required for successful formation and bonding of the patina to the metal. Further, in many cases it is necessary to apply a top coat to the patina to prevent loss of the patina.
More specifically, U.S. patent No. 3,152,927 discloses a formulation for an artificial patina which can be applied in the manufacturing plant to produce a pre-patinated copper sheet. These sheets can then be installed at the chosen site. The patination process comprises producing a basic copper nitrate sludge (with excess Cu(OH)_) which is then applied to oxidised copper sheets and allowed to dry.
The artificial patina coating formed is, however, a basic copper nitrate and is unstable and will undergo competitive reaction to convert the patina to the natural form. This can result in peeling of the applied patina.
Tests by the International Copper Research Association (INCRA project 47c, 1967) revealed that the nitrate patina is not 100% stable with some atmospherically exposed samples performing well in some areas and poorly in others. The initial strength or adhesion of the patina is only moderate with loss of patina occurring at scuff or bend marks due to the brittleness of the coating.
From 1963 to 1967 the International Copper Research Association (INCRA project 47c, 1967) funded a research program to produce an artificial patination process. As a result of this work INCRA Patine 60(b), a solution (paste) of chemicals capable of producing a patina-like coating on copper, was developed. The paste, contains a mixture of copper sulphate, ammonium sulphate, lithium chloride, sodium dichromate, Ben-A-Gel EW and water, and is mixed with hydrochloric acid and then applied to the copper surface with a brush. The patina develops over a few days (and is sensitive to rain or dew during this time) . The final patina developed is chemically different to a natural patina and contains various residual chemicals (eg. LiCl) in the coating from the patinating solution. A clear top-coat after application was shown to greatly improve the success rate of the patina.
Disadvantages of this patination process is the expensive chemicals involved and the high labour costs. In addition the reaction time (a few days) is long and can be easily interrupted by natural weather cycles. Results are fairly variable and somewhat unreliable.
The Copper and Brass Research Association (CABRA) ("Artificial Patination" from Copper Roofing CDA Publication No. 57, 1959) developed a spray method for the coating of large copper objects (eg. roofs) . The spray solution comprises ammonium sulphate, copper sulphate, ammonia and water. The solution is sprayed onto the surface and allowed to dry. This is repeated five to six times . The development of colour depends on suitable weather conditions and rain within eight hours can wash away the solution before the reaction has started. Ideal conditions need fog or a relative humidity of at least 80%.
Disadvantages of this process is that the results of the patination reaction are unreliable and subject to strict atmospheric conditions . In addition the patina formed has a low adhesion and poor weathering qualities.
U.S. Patent No. 3,497,401 describes immersion of copper sheets in an acidic solution (pH = 3.0) containing potassium chlorate (oxidising agent) and copper sulphate. The sheets obtained a patina after about 4 days . This patina is chemically identical to a natural patina but has a different microstructural morphology resulting in easy removal of most of the blue coating. The patina is also a bright blue colour and not the natural blue-green. Major difficulties were experienced in semi-commercial scale production due to the changing solution chemistry (eg. chloride content) of the bath resulting in poor control of the process . The pre-patinated sheets performed well when installed on exposure racks or a roof.
Kobe Steel Ltd (Japan) (Toso Kogaku (Coatings Technology) volume 24 number 7 pages 271-275, 1989) developed a technology allowing the production of an artificial patina in a continuous fashion. The method involves treating a clean plain copper sheet with a colouring agent based on basic copper chloride (atacamite) . This coloured layer is applied with a roller and an upper layer of water based acrylic emulsion resin is sprayed over the top to ensure adhesion of the colour film. It is believed that this upper layer treatment will disappear with time and that the basic copper chloride coloured layer will react to form the naturally occurring patina.
The artificial patina formed has excellent adhesion properties and can withstand severe metalworking (bending, deep drawing) . In addition accelerated corrosion tests and atmospheric exposure tests have indicated that the artificial patina will react to form the naturally occurring compounds.
Disadvantages of this process is the artificial and uniform colour produced. Natural patinas have a blue-green cast and a streaky, mottled appearance. In addition the coating is softer than a natural patina and can be abraded or peeled off due to the continuous acrylic layer.
It is therefore an object of this invention to provide a process and formulation capable of producing a patina which resembles natural patina as closely as possible with regard to composition, morphology and appearance and which has sufficient strength and adhesion over time.
DISCLOSURE OF THE INVENTION
According to a first aspect of the present invention, there is provided an artificial patination formulation comprising:
(a) the reaction product of copper sulphate and optionally iron sulphate, with an inorganic hydroxide compound; and
(b) a suitable binder.
According to a second aspect of the present invention, there is provided a method of coating a copper substrate with an artificial patina, which method comprises applying to the substrate a formulation according to the first aspect.
According to a third aspect of the invention, there is provided a method of coating a copper substrate with an artificial patina, which method comprises contacting the copper substrate with a persulphate solution, and then allowing the contacted surface to oxidize in a high humidity atmosphere.
PREFERRED EMBODIMENT OF THE INVENTION
The copper substrate can be any copper or copper alloy. The substrate will typically be in fabricated or sheet form which may or may not have been pickled and/or acid-cleaned. In particular, copper sheeting roofing panels manufactured from copper electrosheet are suitable. Copper "electrosheet" is copper cathode prepared by the electrolytic refining of copper anodes .
Preferably, the substrate is oxidized. Typically an aged electrosheet (eg. a four week old electrosheet exhibiting a 3 to 6 micrometer oxide film) will be used .
However, if preferred the substrate may be pretreated with an oxidizing procedure.
The formulation can be applied to the copper substrate after installation or can be applied before installation as part of an in-line manufacturing process of the substrate. The formulation can be applied by any suitable application process, typically paintbrush, spray process or by rolling.
Preferably the hydroxide compound is an alkali metal hydroxide such as sodium hydroxide, potassium hydroxide, an alkaline earth metal hydroxide such as barium hydroxide, a transition metal hydroxide or an ammonium hydroxide. Most preferably the hydroxide is sodium hydroxide.
Preferably, the iron sulphate is added in an amount to provide a patina containing up to 10 wt% iron.
Typically, the reaction product is formed by dissolving copper sulphate pentahydrate (eg. 500 g) with iron sulphate heptahydrate (eg. 25 g) in water (eg. 4L) , and then adding sodium hydroxide (eg. IM, 40 g/L, 3.132L) preferably quickly so as to form a fine precipitate. Preferably, the final reaction product has a composition:
( (CU0.957 Fe0.043)SO4)3 ( (Cu0.957 Fe0.043} (0H) 2) which corresponds to a material containing 53.8 wt% Cu, 2.1 wt% Fe, 21.2 wt% S04 and 22.6 wt% OH. The composition however, can preferably be varied between (CuS04)3(Cu(0H)2) to
A suitable binder includes inorganic silicates preferably water-borne, inorganic silicates such as
Zincanode™ 215 available from ICI-Dulux.
Zincanode™ 215 is a high ratio, high build water-borne self curing inorganic silicate.
Typically, lOOg to l,000g of the reaction product is used per 1 litre of binder, more preferably 350g to 450g per litre.
To further assist in adhesion of the formulation to the copper substrate the formulation may further comprise a carboxylic acid. Suitable carboxylic acids include oxalic acid, capric acid, citric acid, tartic acid, D.L. malic acid, sebacic acid, benzoic acid, succinic acid and stearic acid. Preferably the carboxylic acid is present in an amount from 0 to 1000 ppm based on the total weight of the formulation.
A patina can also be formed by contacting the copper substrate with a strong oxidant such as a persulphate solution. Preferably the solution of persulphate is a solution of sodium or ammonium persulphate (typically containing between 10 and 200 g/L in the pH range 3 to 8) . The copper substrate can be contacted by spraying the solution onto the substrate. The contacted surface is then allowed to oxidise in high humidity, typically 95% relative humidity by placing the substrate into a humidity cabinet or conducting the process in a natural high humidity environment. An artificial patina on the substrate results. The substrate can then be washed to remove any residual sodium sulphate.
The invention will now be described by way of example only with reference to the following Examples.
EXAMPLE 1 Dissolve 500g CuSO4.5H20 and 25g FeSO .7H_0 in 4 litres of water. Add 3.1 litres of IM NaOH (40g/litre) solution. Wash and dry precipitate to produce a "dry" powder. Add 350g of powder to 1 litre of water borne inorganic silicate (Zincanode 215), mix and apply to copper surface.
EXAMPLE 2 Dissolve 500g CuS0..5H20 and 5g FeS0..7H20 in 4 litres of water. Add 2.9 litres of IM NaOH (40g/litre) solution. Wash and dry precipitate to produce a "dry" powder. Add 650g of powder to 1 litre of water borne inorganic silicate (Zincanode 215), mix and apply to copper surface.
EXAMPLE 3 Dissolve 500g CuSO..H20 and 15g FeS0..7H20 in 4 litres of water. Add 3.0 litres of IM KOH solution. Wash and dry precipitate to produce a "dry" powder. Add 450g of powder and lOOmg oxalic acid to 1 litre of water borne inorganic silicate (Zincanode 215) , mix and apply to copper surface.
EXAMPLE 4
Dissolve 500g CuS0..5H20 and 7.5g FeS04.7H20 in 4 litres of water. Add 2.9 litres of IM NH OH solution. Wash and dry precipitate to produce a "dry" powder. Add 500g of powder and 100 mg D.L. malic acid to 1 litre of organic silicate (Zincanode 304), mix and apply to copper surface.
EXAMPLE 5
Dissolve 500g CuS04.5H20 in 4 litres of water. Add 3.1 litres of IM NaOH (40g/litre) solution. Wash and dry (spray dry) precipitate to produce a "dry" powder. Add 350g of powder and 25mg D.L. malic acid to 1 litre of water borne inorganic silicate (Zincanode 215) , mix and apply to copper surface.
EXAMPLE 6
Dissolve 50g sodium persulfate in 1 litre of water. Adjust pH to 8 with NaOH. Spray solution onto copper surface. Age for 2 hours in high humidity environment (>95%RH) . Allow to dry slowly, then wash surface. Repeated twice,- gave desired surface patination.
EXAMPLE 7
Dissolve lOg sodium persulfate in 1 litre of water. Adjust pH to 7 with NaOH. Spray solution onto copper surface. Age for 2 hours in high humidity environment (>95%RH) . Allow to dry slowly, then wash surface. Repeated ten times,- gave desired surface patination.
The processes and formulations of the present invention are suitable for forming a patina on any copper substrate.

Claims

CLAIMS : -
1. An artificial patination formulation comprising:
(a) the reaction product of copper sulfate and optionally iron sulphate, with an inorganic hydroxide compound; and
(b) a suitable binder.
2. A formulation according to claim 1, wherein the hydroxide compound is an alkali metal hydroxide, an alkaline earth metal hydroxide, a transition metal hydroxide or ammonium hydroxide.
3. A formulation according to claim 2 wherein the hydroxide compound is sodium hydroxide.
4. A formulation according to any one of claims 1 to 3 wherein the binder is an inorganic silicate.
5. A formulation according to claim 4 wherein the silicate is a water borne, inorganic silicate.
6. A formulation according to any one of claims 1 to 5 further comprising a carboxylic acid.
7. A formulation according to claim 6 wherein the carboxylic acid is oxalic acid, capric acid, citric acid, tartic acid, D.L malic acid, sebacic acid, benzoic acid, succinic acid or stearic acid.
8. A formulation according to claim 6 or 7 wherein the carboxylic acid is present in an amount of from 0 to 1000 ppm based on the total weight of the formulation.
9. A formulation according to any one of claims 1 to 8 wherein the reaction product has a composition varied between (CuSO.)3Cu(OH) and
( (Cu0.8Fe0.2,SO43( (Cu0.8Pe0.2, (OH)2)-
10. A formulation according to any one of claims 1 to
9 containing 100 to 1,000 g of reaction product per litre of binder.
11. A method of coating a copper substrate with an artificial patina, comprising applying to the substrate a formulation according to any one of claims 1 to 10.
12. A method according to claim 11 wherein the copper substrate is copper or a copper alloy.
13. A method according to claim 11 or 12 wherein the substrate is in fabricated or sheet form which has optionally been pickled and/or acid cleaned.
14. A method according to any one of claims 11 to 13 where the substrate is copper electrosheet.
15. A method according to any one of claims 11 to 14 wherein the substrate is oxidized prior to application of the formulation.
16. A method according to any one of claims 11 to 15 wherein the formulation is applied by paintbrush, spraying or by rolling.
17. A method according to any one of claims 11 to 16 wherein the formulation is applied after installation or before installation as part of an in-line manufacturing process of the substrate.
18. A method of coating a copper substrate with an artificial patina comprising contacting the copper substrate with a persulphate solution and then allowing the contacted surface to oxidize in a high humidity atmosphere.
19. A method according to claim 18 wherein the persulphate solution contains sodium or ammonium persulphate.
20. A method of claim 18 or 19 wherein the persulphate solution contains between 10 g/L to 200 g/L of the persulphate.
21. A method according to any one of claims 18 to 20 wherein the persulphate solution has a pH from 3 to 8
22. A method according to any one of claims 18 to 21 wherein the persulphate solution is applied by spraying.
23. A method according to any one of claims 18 to 22 wherein the relative humidity of the atmosphere is 95'
EP95916502A 1994-04-26 1995-04-21 Artificial patina Withdrawn EP0797631A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPM5294A AUPM529494A0 (en) 1994-04-26 1994-04-26 Artificial patina
AUPM0529/49 1994-04-26
PCT/AU1995/000236 WO1995029207A1 (en) 1994-04-26 1995-04-21 Artificial patina

Publications (2)

Publication Number Publication Date
EP0797631A1 true EP0797631A1 (en) 1997-10-01
EP0797631A4 EP0797631A4 (en) 1998-05-06

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EP95916502A Withdrawn EP0797631A4 (en) 1994-04-26 1995-04-21 Artificial patina

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EP (1) EP0797631A4 (en)
JP (1) JPH10503224A (en)
AU (1) AUPM529494A0 (en)
CA (1) CA2188661A1 (en)
WO (1) WO1995029207A1 (en)

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ITMI20020307A1 (en) * 2002-02-15 2003-08-18 Beretta Armi Spa PROCEDURE FOR CONFERRING A TURTLE CHROMATIC EFFECT TO METAL SUBSTRATES
FI20020669A (en) 2002-04-09 2003-10-10 Outokumpu Oy Procedure for preparing artificial patina and a patina paste
KR20030088550A (en) * 2002-05-13 2003-11-20 김부현 manufacturing method of oxidized copper plate for construction materials
KR100467939B1 (en) * 2002-05-13 2005-01-24 김부현 oxidation preparation of manucturing for oxidized copper plate of construction materials
DE10243139A1 (en) * 2002-09-17 2004-03-25 Omg Galvanotechnik Gmbh Alloy for decorative or functional purposes e.g. as a coating material for buttons and sliding clasp fasteners and absorbing layers in solar cells contains tin, copper, bismuth and oxidic oxygen
DE102006053192A1 (en) 2006-11-09 2008-05-15 Kme Germany Ag Process for protecting patinated surfaces of copper products and patinated copper product
KR101678135B1 (en) * 2015-09-15 2016-11-21 포항공과대학교 산학협력단 patina forming method
CN109988477A (en) * 2019-04-23 2019-07-09 广东金涂宝新材料股份有限公司 The aqueous imitative iron rust coating of one kind and its construction method
CN111549336A (en) * 2020-04-02 2020-08-18 福建捷思金属科技发展有限公司 Pre-oxidation thermal coloring method for verdigris

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JPS5935937B2 (en) * 1974-07-16 1984-08-31 関西ペイント株式会社 water-based paint composition
JPS52131236A (en) * 1976-04-26 1977-11-04 Sekisui Chem Co Ltd Solar energy absorber
AU532049B2 (en) * 1980-02-01 1983-09-15 Cook Paint & Varnish Co. Zinc rich paints having silicate and titanate ester copoly- mer binder

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Title
No further relevant documents disclosed *
See also references of WO9529207A1 *

Also Published As

Publication number Publication date
JPH10503224A (en) 1998-03-24
EP0797631A4 (en) 1998-05-06
AUPM529494A0 (en) 1994-05-19
WO1995029207A1 (en) 1995-11-02
CA2188661A1 (en) 1995-11-02

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