Anodizing

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These carabiners have an anodized aluminium surface that has been dyed; they are made in many colors.

Anodizing (also spelled anodising, particularly in the UK and Australia) is an electrolytic passivation process used to increase the thickness of the natural oxide layer on the surface of metal parts.

The process is called anodizing because the part to be treated forms the anode electrode of an electrical circuit. Anodizing increases corrosion resistance and wear resistance, and provides better adhesion for paint primers and glues than does bare metal. Anodic films can also be used for a number of cosmetic effects, either with thick porous coatings that can absorb dyes or with thin transparent coatings that add interference effects to reflected light.

Anodizing is also used to prevent galling of threaded components and to make dielectric films for electrolytic capacitors. Anodic films are most commonly applied to protect aluminium alloys, although processes also exist for titanium, zinc, magnesium, niobium, zirconium, hafnium, and tantalum. Iron or carbon steel metal exfoliates when oxidized under neutral or alkaline microelectrolytic conditions; i.e., the iron oxide (actually ferric hydroxide or hydrated iron oxide, also known as rust) forms by anoxic anodic pits and large cathodic surface, these pits concentrate anions such as sulfate and chloride accelerating the underlying metal to corrosion. Carbon flakes or nodules in iron or steel with high carbon content (high carbon steel, cast iron) may cause an electrolytic potential and interfere with coating or plating. Ferrous metals are commonly anodized electrolytically in nitric acid, or by treatment with red fuming nitric acid, to form hard black ferric oxide. This oxide remains conformal even when plated on wire and the wire is bent.

Anodization changes the microscopic texture of the surface and changes the crystal structure of the metal near the surface. Thick coatings are normally porous, so a sealing process is often needed to achieve corrosion resistance. Anodized aluminium surfaces, for example, are harder than aluminium but have low to moderate wear resistance that can be improved with increasing thickness or by applying suitable sealing substances. Anodic films are generally much stronger and more adherent than most types of paint and metal plating, but also more brittle. This makes them less likely to crack and peel from aging and wear, but more susceptible to cracking from thermal stress.

History[edit]

Anodizing was first used on an industrial scale in 1923 to protect Duralumin seaplane parts from corrosion. This early chromic acid–based process was called the Bengough-Stuart process and was documented in British defence specification DEF STAN 03-24/3. It is still used today despite its legacy requirements for a complicated voltage cycle now known to be unnecessary. Variations of this process soon evolved, and the first sulfuric acid anodizing process was patented by Gower and O'Brien in 1927. Sulfuric acid soon became and remains the most common anodizing electrolyte.[1]

Oxalic acid anodizing was first patented in Japan in 1923 and later widely used in Germany, particularly for architectural applications. Anodized aluminium extrusion was a popular architectural material in the 1960s and 1970s, but has since been displaced by cheaper plastics and powder coating.[2] The phosphoric acid processes are the most recent major development, so far only used as pretreatments for adhesives or organic paints.[1] A wide variety of proprietary and increasingly complex variations of all these anodizing processes continue to be developed by industry, so the growing trend in military and industrial standards is to classify by coating properties rather than by process chemistry.

Anodized aluminium[edit]

Aluminium alloys are anodized to increase corrosion resistance and to allow dyeing (coloring), improved lubrication, or improved adhesion.However, anodizing does not increase the strength of the aluminium object. The anodic layer is non-conductive.[3]

When exposed to air at room temperature, or any other gas containing oxygen, pure aluminium self-passivates by forming a surface layer of amorphous aluminium oxide 2 to 3 nm thick,[4] which provides very effective protection against corrosion. Aluminium alloys typically form a thicker oxide layer, 5-15 nm thick, but tend to be more susceptible to corrosion. Aluminium alloy parts are anodized to greatly increase the thickness of this layer for corrosion resistance. The corrosion resistance of aluminium alloys is significantly decreased by certain alloying elements or impurities: copper, iron, and silicon,[5] so 2000, 4000, and 6000-series Al alloys tend to be most susceptible.

Although anodizing produces a very regular and uniform coating, microscopic fissures in the coating can lead to corrosion. Further, the coating is susceptible to chemical dissolution in the presence of high and low pH chemistry, which results in stripping the coating and corrosion of the substrate. To combat this, various techniques have been developed either to reduce the number of fissures or to insert more chemically stable compounds into the oxide, or both. For instance, sulfuric anodized articles are normally sealed, either through hydro-thermal sealing or precipitating sealing, to reduce porosity and interstitial pathways that allow for corrosive ion exchange between the surface and the substrate. Precipitating seals enhance chemical stability but are less effective in eliminating ion exchange pathways. Most recently, new techniques to partially convert the amorphous oxide coating into more stable micro-crystalline compounds have been developed that have shown significant improvement based on shorter bond lengths.

Some aluminium aircraft parts, architectural materials, and consumer products are anodized. Anodized aluminium can be found on mp3 players, smartphones, multi-tools, flashlights, cookware, cameras, sporting goods, window frames, roofs, in electrolytic capacitors, and on many other products both for corrosion resistance and the ability to retain dye. Although anodizing only has moderate wear resistance, the deeper pores can better retain a lubricating film than a smooth surface would.

Anodized coatings have a much lower thermal conductivity and coefficient of linear expansion than aluminium. As a result, the coating will crack from thermal stress if exposed to temperatures above 80 °C. The coating can crack, but it will not peel.[6] The melting point of aluminium oxide is 2050 °C, much higher than pure aluminium's 658 °C.[6] This and the non-conductivity of aluminum oxide can make welding more difficult.

In typical commercial aluminium anodization processes, the aluminium oxide is grown down into the surface and out from the surface by equal amounts.[7] So anodizing will increase the part dimensions on each surface by half the oxide thickness. For example, a coating that is 2 μm thick will increase the part dimensions by 1 μm per surface. If the part is anodized on all sides, then all linear dimensions will increase by the oxide thickness. Anodized aluminium surfaces are harder than aluminium but have low to moderate wear resistance, although this can be improved with thickness and sealing.

Process[edit]

The anodized aluminium layer is grown by passing a direct current through an electrolytic solution, with the aluminium object serving as the anode (the positive electrode). The current releases hydrogen at the cathode (the negative electrode) and oxygen at the surface of the aluminium anode, creating a build-up of aluminium oxide. Alternating current and pulsed current is also possible but rarely used. The voltage required by various solutions may range from 1 to 300 V DC, although most fall in the range of 15 to 21 V. Higher voltages are typically required for thicker coatings formed in sulfuric and organic acid. The anodizing current varies with the area of aluminium being anodized, and typically ranges from 30 to 300 amperes/meter² (2.8 to 28 ampere/ft²).

Aluminium anodizing is usually performed in an acid solution which slowly dissolves the aluminium oxide. The acid action is balanced with the oxidation rate to form a coating with nanopores, 10-150 nm in diameter.[6] These pores are what allow the electrolyte solution and current to reach the aluminium substrate and continue growing the coating to greater thickness beyond what is produced by autopassivation.[8] However, these same pores will later permit air or water to reach the substrate and initiate corrosion if not sealed. They are often filled with colored dyes and/or corrosion inhibitors before sealing. Because the dye is only superficial, the underlying oxide may continue to provide corrosion protection even if minor wear and scratches may break through the dyed layer.

Conditions such as electrolyte concentration, acidity, solution temperature, and current must be controlled to allow the formation of a consistent oxide layer. Harder, thicker films tend to be produced by more dilute solutions at lower temperatures with higher voltages and currents. The film thickness can range from under 0.5 micrometers for bright decorative work up to 150 micrometers for architectural applications.

Other widely used specifications[edit]

The most widely used anodizing specification is a U.S. military spec, MIL-A-8625, which defines three types of aluminium anodization. Type I is chromic acid anodization, Type II is sulfuric acid anodization, and Type III is sulfuric acid hardcoat anodization. Other anodizing specifications include more MIL-SPECs (e.g., MIL-A-63576), aerospace industry specs by organizations such as SAE, ASTM, and ISO (e.g., AMS 2469, AMS 2470, AMS 2471, AMS 2472, AMS 2482, ASTM B580, ASTM D3933, ISO 10074, and BS 5599), and corporation-specific specs (such as those of Boeing, Lockheed Martin, and other large contractors). AMS 2468 is obsolete. None of these specifications define a detailed process or chemistry, but rather a set of tests and quality assurance measures which the anodized product must meet. BS 1615 provides guidance in the selection of alloys for anodizing. For British defence work, a detailed chromic and sulfuric anodizing processes are described by STAN 03-24/3 and STAN 03-25/3 respectively.

Chromic acid anodizing (Type I)[edit]

The oldest anodizing process uses chromic acid. It is widely known as the Bengough-Stuart process. In North America it is known as Type I because it is so designated by the MIL-A-8625 standard, but it is also covered by AMS 2470 and MIL-A-8625 Type IB. In the UK it is normally specified as Def Stan 03/24 and used in areas that are prone to come into contact with propellants etc. There are also Boeing and Airbus standards. Chromic acid produces thinner, 0.5 μm to 18 μm (0.00002" to 0.0007")[9] more opaque films that are softer, ductile, and to a degree self-healing. They are harder to dye and may be applied as a pretreatment before painting. The method of film formation is different from using sulfuric acid in that the voltage is ramped up through the process cycle.

Sulfuric acid anodizing (Type II & III)[edit]

Sulfuric acid is the most widely used solution to produce anodized coating. Coatings of moderate thickness 1.8 μm to 25 μm (0.00007" to 0.001")[9] are known as Type II in North America, as named by MIL-A-8625, while coatings thicker than 25 μm (0.001") are known as Type III, hardcoat, hard anodizing, or engineered anodizing. Very thin coatings similar to those produced by chromic anodizing are known as Type IIB. Thick coatings require more process control,[6] and are produced in a refrigerated tank near the freezing point of water with higher voltages than the thinner coatings. Hard anodizing can be made between 13 and 150 μm (0.0005" to 0.006") thick. Anodizing thickness increases wear resistance, corrosion resistance, ability to retain lubricants and PTFE coatings, and electrical and thermal insulation. Standards for thin (Soft/Standard) sulfuric anodizing are given by MIL-A-8625 Types II and IIB, AMS 2471 (undyed), and AMS 2472 (dyed), BS EN ISO 12373/1 (decorative), BS EN 3987 (Architectural) . Standards for thick sulfuric anodizing are given by MIL-A-8625 Type III, AMS 2469, BS 5599, BS EN 2536 and the obsolete AMS 2468 and DEF STAN 03-26/1.

Organic acid anodizing[edit]

Anodizing can produce yellowish integral colors without dyes if it is carried out in weak acids with high voltages, high current densities, and strong refrigeration.[6] Shades of color are restricted to a range which includes pale yellow, gold, deep bronze, brown, grey, and black. Some advanced variations can produce a white coating with 80% reflectivity. The shade of color produced is sensitive to variations in the metallurgy of the underlying alloy and cannot be reproduced consistently.[2]

Anodization in some organic acids, for example malic acid, can enter a 'runaway' situation, in which the current drives the acid to attack the aluminum far more aggressively than normal, resulting in huge pits and scarring. Also, if the current or voltage are driven too high, 'burning' can set in; in this case the supplies act as if nearly shorted and large, uneven and amorphous black regions develop.

Integral color anodizing is generally done with organic acids, but the same effect has been produced in laboratory with very dilute sulfuric acid. Integral color anodizing was originally performed with oxalic acid, but sulfonated aromatic compounds containing oxygen, particularly sulfosalicylic acid, have been more common since the 1960s.[2] Thicknesses up to 50μm can be achieved. Organic acid anodizing is called Type IC by MIL-A-8625.

Phosphoric acid anodizing[edit]

Anodizing can be carried out in phosphoric acid, usually as a surface preparation for adhesives. This is described in standard ASTM D3933.

Borate and tartrate baths[edit]

Anodizing can also be performed in borate or tartrate baths in which aluminium oxide is insoluble. In these processes, the coating growth stops when the part is fully covered, and the thickness is linearly related to the voltage applied.[6] These coatings are free of pores, relative to the sulfuric and chromic acid processes.[6] This type of coating is widely used to make electrolytic capacitors, because the thin aluminium films (typically less than 0.5 μm) would risk being pierced by acidic processes.[1]

Plasma electrolytic oxidation[edit]

Plasma electrolytic oxidation is a similar process, but where higher voltages are applied. This causes sparks to occur, and results in more crystalline/ceramic type coatings.

Other metals[edit]

Anodized titanium[edit]

Selected colors achievable through anodization of titanium.

Anodized titanium is used in a recent generation of dental implants. An anodized oxide layer has a thickness in the range of 30 nanometers (1.2×10−6 in) to several micrometers.[10] Standards for titanium anodizing are given by AMS 2487 and AMS 2488.

Anodizing titanium generates an array of different colors without dyes, for which it is sometimes used in art, costume jewelry, body piercing jewelry and wedding rings. The color formed is dependent on the thickness of the oxide (which is determined by the anodizing voltage); it is caused by the interference of light reflecting off the oxide surface with light traveling through it and reflecting off the underlying metal surface.

Anodized magnesium[edit]

Magnesium is anodized primarily as a primer for paint. A thin (5μm) film is sufficient for this.[11] Thicker coatings of 25μm and up can provide mild corrosion resistance when sealed with oil, wax, or sodium silicate.[11] Standards for magnesium anodizing are given in AMS 2466, AMS 2478, AMS 2479, and ASTM B893.

Anodized zinc[edit]

Zinc is rarely anodized, but a process was developed by the International Lead Zinc Research Organization and covered by MIL-A-81801.[11] A solution of ammonium phosphate, chromate and fluoride with voltages of up to 200V can produce olive green coatings up to 80μm thick.[11] The coatings are hard and corrosion resistant.

Zinc or Galvanized steel can be anodized at lower voltages(20-30V)as well using direct currents from silicate baths containing varying concentration of sodium silicate, sodium hydroxide, borax, sodium nitrite and nickel sulphate.[12]

Anodized niobium[edit]

Niobium anodizes in a similar fashion to titanium with a range of attractive colors being formed by interference at different film thicknesses. Again the film thickness is dependent on the anodizing voltage.[13][14] Uses include jewelry and commemorative coins.

Anodized tantalum[edit]

Tantalum anodizes in a similar fashion to titanium and niobium with a range of attractive colors being formed by interference at different film thicknesses. Again the film thickness is dependent on the anodizing voltage and typically ranges from 18-23 Angstroms per volt depending on electrolyte and temperature. Uses include Tantalum capacitors.

Dyeing[edit]

Colored iPod Mini cases are dyed following anodization and before thermal sealing

The most common anodizing processes, for example sulfuric acid on aluminium, produce a porous surface which can accept dyes easily. The number of dye colors is almost endless; however, the colors produced tend to vary according to the base alloy. Though some may prefer lighter colors, in practice they may be difficult to produce on certain alloys such as high-silicon casting grades and 2000-series aluminium-copper alloys. Another concern is the "lightfastness" of organic dyestuffs—some colors (reds and blues) are particularly prone to fading. Black dyes and gold produced by inorganic means (ferric ammonium oxalate) are more lightfast. Dyed anodizing is usually sealed to reduce or eliminate dye bleed out.

Alternatively, metal (usually tin) can be electrolytically deposited in the pores of the anodic coating to provide colors that are more lightfast. Metal dye colors range from pale champagne to black. Bronze shades are commonly used for architectural use.

Alternatively the color may be produced integral to the film. This is done during the anodizing process using organic acids mixed with the sulfuric electrolyte and a pulsed current.

Splash effects are created by dying the unsealed porous surface in lighter colors and then splashing darker color dyes onto the surface. Aqueous and solvent based dye mixtures may also be alternately applied since the colored dyes will resist each other and leave spotted effects.

Printing[edit]

Photo quality images and graphics in vivid color may be printed into the unsealed porous oxide layer using color dyes via silkscreen, sublimation transfer or digital printer. Line art quality graphics can be achieved by use of a printer. Color graphics may also be directly applied by hand using an airbrush, sponge or paintbrush. Printed anodizing is sealed to prevent or reduce dye bleed out. Uses include baseball bats, signs, furniture, surgical trays, motorcycle components, and architectural moulding.

Sealing[edit]

Acidic anodizing solutions produce pores in the anodized coating. These pores can absorb dyes and retain lubricants, but are also an avenue for corrosion. When lubrication properties are not critical, they are usually sealed after dyeing to increase corrosion resistance and dye retention. Long immersion in boiling-hot deionized water or steam is the simplest sealing process, although it is not completely effective and reduces abrasion resistance by 20%.[6] The oxide is converted into its hydrated form, and the resulting swelling reduces the porosity of the surface. Cold sealing, where the pores are closed by impregnation of a sealant in a room-temperature bath, is more popular due to energy savings. Coatings sealed in this method are not suitable for adhesive bonding. Teflon, nickel acetate, cobalt acetate, and hot sodium or potassium dichromate seals are commonly used. MIL-A-8625 requires sealing for thin coatings (Types I and II) and allows it as an option for thick ones (Type III).

Cleaning[edit]

Anodized aluminium surfaces are susceptible to Panel Edge Staining, a unique type of surface staining that can affect the structural integrity of the metal.

Environmental impact[edit]

Anodizing is one of the more environmentally friendly metal finishing processes. With the exception of organic (aka integral color) anodizing, the by-products contain only small amounts of heavy metals, halogens, or volatile organic compounds. Integral color anodizing produces no VOCs, Heavy Metals, or Halogens as all of the byproducts found in the effluent streams of other processes come from their dyes or plating materials.[15] The most common anodizing effluents, aluminium hydroxide and aluminium sulfate, are recycled for the manufacturing of alum, baking powder, cosmetics, newsprint and fertilizer or used by industrial wastewater treatment systems.

Mechanical considerations[edit]

Anodizing will raise the surface, since the oxide created occupies more space than the base metal converted. This will generally not be of consequence except where there are small tolerances. If so, the thickness of the anodizing has to be taken into account when choosing the machining dimension. Also in the case of small holes threaded to accept screws,[citation needed] anodizing may cause the screws to bind, thus the threaded holes may need to be chased with a tap to restore the original dimensions. Alternatively, special oversize taps may be used to precompensate for this growth. In the case of unthreaded holes that accept fixed diameter pins or rods, a slightly oversized hole to allow for the dimension change may be appropriate.

References[edit]

  1. ^ a b c Sheasby & Pinner 2001, pp. 427–596.
  2. ^ a b c Sheasby & Pinner 2001, pp. 597–742.
  3. ^ Davis 1993, p. 376.
  4. ^ Sheasby & Pinner 2001, p. 5.
  5. ^ Sheasby & Pinner 2001, p. 9.
  6. ^ a b c d e f g h Edwards, Joseph (1997). Coating and Surface Treatment Systems for Metals. Finishing Publications Ltd. and ASM International. pp. 34–38. ISBN 0-904477-16-9. 
  7. ^ Kutz, Myer. "Protective coatings for aluminum alloys". Handbook of Environmental Degradation of Materials. Norwich, NY: William Andrew. p. 353. ISBN 978-0-8155-1749-8. 
  8. ^ Sheasby & Pinner 2001, pp. 327–425.
  9. ^ a b US Military Specification MIL-A-8625, ASSIST database
  10. ^ http://www.ecmjournal.org/journal/supplements/vol005supp01/pdf/vol005supp01a18.pdf
  11. ^ a b c d Edwards, Joseph (1997). Coating and Surface Treatment Systems for Metals. Finishing Publications Ltd. and ASM International. pp. 39–40. ISBN 0-904477-16-9. 
  12. ^ ANODIZING OF ZINC FOR IMPROVED SURFACE PROPERTIES M. A. Imam1, M. Moniruzzaman2 & M. A. Mamun3 1Centre for Environmental Safety and Risk Engineering, Victoria University, Australia 2Department of Materials & Metallurgical Engineering, Bangladesh University of Engineering & Technology (BUET), Dhaka-1000, 3Bangladesh 3Materials Science Division, Bangladesh Atomic Energy Commission, Dhaka-1000, Bangladesh, 18th International Corrosion Congress ,Perth, November 2011,ISSN 1326 1932 Anodizing of Zinc
  13. ^ Biason Gomes, M. A.; S. Onofre, S. Juanto, L. O. de S. Bulhões (1991). "Anodization of niobium in sulphuric acid media". Journal of Applied Electrochemistry 21 (11): 1023–1026. doi:10.1007/BF01077589. 
  14. ^ Chiou, Y. L. (1971). "A note on the thicknesses of anodized niobium oxide films". Thin Solid Films 8 (4): R37–R39. Bibcode:1971TSF.....8R..37C. doi:10.1016/0040-6090(71)90027-7. 
  15. ^ "Anodizing and the environment". Archived from the original on 8 September 2008. Retrieved 2008-09-08. 

Bibliography[edit]

  • Davis, Joseph R. (1993). Aluminum and Aluminum Alloys (4th ed.). ASM International. ISBN 978-0-87170-496-2. OCLC 246875365. 
  • Sheasby, P. G.; Pinner, R. (2001). The Surface Treatment and Finishing of Aluminum and its Alloys 2 (sixth ed.). Materials Park, Ohio & Stevenage, UK: ASM International & Finishing Publications. ISBN 0-904477-23-1. 

External links[edit]