Passivation (chemistry)
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Passivation Chemistry

Passivation, in physical chemistry and engineering, refers to a material becoming "passive," that is, less affected or corroded by the environment of future use. Passivation involves creation of an outer layer of shield material that is applied as a microcoating, created by chemical reaction with the base material, or allowed to build from spontaneous oxidation in the air. As a technique, passivation is the use of a light coat of a protective material, such as metal oxide, to create a shell against corrosion.[1] Passivation can occur only in certain conditions, and is used in microelectronics to enhance silicon.[2] The technique of passivation strengthens and preserves the appearance of metallics. In electrochemical treatment of water, passivation reduces the effectiveness of the treatment by increasing the circuit resistance, and active measures are typically used to overcome this effect, the most common being polarity reversal, which results in limited rejection of the fouling layer. Other proprietary systems to avoid electrode passivation, several discussed below, are the subject of ongoing research and development.

When exposed to air, many metals naturally form a hard, relatively inert surface, as in the tarnish of silver. In the case of other metals, such as iron, a somewhat rough porous coating is formed from loosely adherent corrosion products. In this case, a substantial amount of metal is removed, which is either deposited or dissolved in the environment. Corrosion coating reduces the rate of corrosion by varying degrees, depending on the kind of base metal and its environment, and is notably slower in room-temperature air for aluminium, chromium, zinc, titanium, and silicon (a metalloid); the shell of corrosion inhibits deeper corrosion, and operates as one form of passivation. The inert surface layer, termed the "native oxide layer", is usually an oxide or a nitride, with a thickness of a monolayer of 0.1-0.3 nm (1-3 Å) for a noble metal such as platinum, about 1.5 nm (15 Å) for silicon, and nearer to 5 nm (50 Å) for aluminium after several years.[3][4][5]


There has been much interest in determining the mechanisms that govern the increase of thickness of the oxide layer over time. Some of the important factors are the volume of oxide relative to the volume of the parent metal, the mechanism of oxygen diffusion through the metal oxide to the parent metal, and the relative chemical potential of the oxide. Boundaries between micro grains, if the oxide layer is crystalline, form an important pathway for oxygen to reach the unoxidized metal below. For this reason, vitreous oxide coatings - which lack grain boundaries - can retard oxidation.[7] The conditions necessary (but not sufficient) for passivation are recorded in Pourbaix diagrams. Some corrosion inhibitors help the formation of a passivation layer on the surface of the metals to which they are applied. Some compounds, dissolving in solutions (chromates, molybdates) form non-reactive and low solubility films on metal surfaces.


In the mid 1800s, Christian Friedrich Schönbein discovered that when a piece of iron is placed in dilute nitric acid, it will dissolve and produce hydrogen, but if the iron is placed in concentrated nitric acid and then returned to the dilute nitric acid, little or no reaction will take place. Schönbein named the first state the active condition and the second the passive condition. If passive iron is touched by active iron, it becomes active again. In 1920, Ralph S. Lillie measured the effect of an active piece of iron touching a passive iron wire and found that "a wave of activation sweeps rapidly (at some hundred centimeters a second) over its whole length".[8][9]

Specific materials



In the area of microelectronics, the formation of a strongly adhering passivating oxide is important to the performance of silicon. Moreover, such thermal oxidation processes are often employed in the fabrication of silicon nanowires and other Si nanostructures.

The method of silicon surface passivation was developed by Mohamed Atalla in 1957. While researching the surface properties of silicon semiconductors at Bell Labs, he proposed a new method of semiconductor device fabrication, coating a silicon wafer with an insulating layer of silicon oxide so that electricity could reliably penetrate to the conducting silicon below. He researched the use of silica as a protective layer of silicon semiconductor devices. By adopting a method of growing a layer of silicon dioxide on top of a silicon wafer, Atalla was able to overcome the surface states that prevented electricity from reaching the semiconducting layer. This is known as surface passivation, a critical step that made possible the ubiquity of silicon integrated circuits, and later became critical to the semiconductor industry.[10][11][11] He published his findings in 1957, and presented it at a 1958 Electrochemical Society meeting.[12][13]

Atalla's surface passivation method was later the basis for two inventions in 1959: the MOSFET (MOS transistor) by Atalla and Dawon Kahng at Bell Labs, and the planar process by Jean Hoerni at Fairchild Semiconductor. The planar process was in turn the basis for Robert Noyce's monolithic integrated circuit (IC) chip, also invented in 1959, at Fairchild.[13]


In the area of photovoltaics, a passivating surface layer such as silicon nitride, silicon dioxide or titanium dioxide can reduce surface recombination - a significant loss mechanism in solar cells. The passivation of silicon, whether desirable or not, by a Silicon dioxide layer is commonly described by the Deal-Grove model.


Pure aluminium naturally forms a thin surface layer of aluminium oxide on contact with oxygen in the atmosphere through a process called oxidation, which creates a physical barrier to corrosion or further oxidation in many environments. Some aluminium alloys, however, do not form the oxide layer well, and thus are not protected against corrosion. There are methods to enhance the formation of the oxide layer for certain alloys. For example, prior to storing hydrogen peroxide in an aluminium container, the container can be passivated by rinsing it with a dilute solution of nitric acid and peroxide alternating with deionized water. The nitric acid and peroxide mixture oxidizes and dissolves any impurities on the inner surface of the container, and the deionized water rinses away the acid and oxidized impurities.[14]

Generally, there are two main ways to passivate aluminium alloys (not counting plating, painting, and other barrier coatings): chromate conversion coating and anodizing. Alclading, which metallurgically bonds thin layers of pure aluminium or alloy to different base aluminium alloy, is not strictly passivation of the base alloy. However, the aluminium layer clad on is designed to spontaneously develop the oxide layer and thus protect the base alloy.

Chromate conversion coating converts the surface aluminium to an aluminium chromate coating in the range of 0.00001-0.00004 inches (250-1,000 nm) in thickness. Aluminium chromate conversion coatings are amorphous in structure with a gel-like composition hydrated with water.[15] Chromate conversion is a common way of passivating not only aluminium, but also zinc, cadmium, copper, silver, magnesium, and tin alloys.

Anodizing is an electrolytic process that forms a thicker oxide layer. The anodic coating consists of hydrated aluminium oxide and is considered resistant to corrosion and abrasion.[16] This finish is more robust than the other processes and also provides electrical insulation, which the other two processes may not.

Ferrous materials

Ferrous materials, including steel, may be somewhat protected by promoting oxidation ("rust") and then converting the oxidation to a metalophosphate by using phosphoric acid and further protected by surface coating. As the uncoated surface is water-soluble, a preferred method is to form manganese or zinc compounds by a process commonly known as parkerizing or phosphate conversion. Older, less-effective but chemically-similar electrochemical conversion coatings included black oxidizing, historically known as bluing or browning. Ordinary steel forms a passivating layer in alkali environments, as reinforcing bar does in concrete.

Stainless steel

The fitting on the left has not been passivated, the fitting on the right has been passivated.

Stainless steels are corrosion-resistant, but they are not completely impervious to rusting. One common mode of corrosion in corrosion-resistant steels is when small spots on the surface begin to rust because grain boundaries or embedded bits of foreign matter (such as grinding swarf) allow water molecules to oxidize some of the iron in those spots despite the alloying chromium. This is called rouging. Some grades of stainless steel are especially resistant to rouging; parts made from them may therefore forgo any passivation step, depending on engineering decisions.[17]

Common among all of the different specifications and types are the following steps: Prior to passivation, the object must be cleaned of any contaminants and generally must undergo a validating test to prove that the surface is 'clean.' The object is then placed in an acidic passivating bath that meets the temperature and chemical requirements of the method and type specified between customer and vendor. (Temperatures can range from ambient to 60 degrees C, or 140 degrees F, while minimum passivation times are usually 20 to 30 minutes). The parts are neutralized using a bath of aqueous sodium hydroxide, then rinsed with clean water and dried. The passive surface is validated using humidity, elevated temperature, a rusting agent (salt spray), or some combination of the three. However, proprietary passivation processes exist[18] for martensitic stainless steel, which is difficult to passivate, as microscopic discontinuities can form in the surface of a machined part during passivation in a typical nitric acid bath.[19] The passivation process removes exogenous iron,[20] creates/restores a passive oxide layer that prevents further oxidation (rust), and cleans the parts of dirt, scale, or other welding-generated compounds (e.g. oxides).[20][21]

Passivation processes are generally controlled by industry standards, the most prevalent among them today being ASTM A 967 and AMS 2700. These industry standards generally list several passivation processes that can be used, with the choice of specific method left to the customer and vendor. The "method" is either a nitric acid-based passivating bath, or a citric acid-based bath, these acids remove surface iron and rust, while sparing the chromium. The various 'types' listed under each method refer to differences in acid bath temperature and concentration. Sodium dichromate is often required as an additive to oxidise the chromium in certain 'types' of nitric-based acid baths, however this chemical is highly toxic. With citric acid, simply rinsing and drying the part and allowing the air to oxidise it, or in some cases the application of other chemicals, is used to perform the passivation of the surface.

It is not uncommon for some aerospace manufacturers to have additional guidelines and regulations when passivating their products that exceed the national standard. Often, these requirements will be cascaded down using Nadcap or some other accreditation system. Various testing methods are available to determine the passivation (or passive state) of stainless steel. The most common methods for validating the passivity of a part is some combination of high humidity and heat for a period of time, intended to induce rusting. Electro-chemical testers can also be utilized to commercially verify passivation.


Nickel can be used for handling elemental fluorine, owing to the formation of a passivation layer of nickel fluoride. This fact is useful in water treatment and sewage treatment applications

See also


  1. ^ "Passivation vs Electropolishing - What are the differences?".
  2. ^ IUPAC Goldbook
  3. ^
  4. ^ O'M. Bockris 1977, p. 1325
  5. ^ Fehlner, Francis P, Low-Temperature Oxidation:The Role of Vitreous Oxides, A Wiley-Interscience Publication, John Wiley & Sons, New York , 1986 ISBN 0471-87448-5
  6. ^ University of Bath Archived 3 March 2009 at the Wayback Machine & Western Oregon University
  7. ^ Fehlner, Francis P, ref.3.
  8. ^ Lillie, Ralph S. (20 June 1920). "The Recovery of Transmissivity in Passive Iron Wires as a Model of Recovery Processes in Irritable Living Systems". The Journal of General Physiology. Physiological Laboratory, Clark University, Worcester. 3 (2): 129-43. doi:10.1085/jgp.3.2.129. PMC 2140424. Retrieved 2015.
  9. ^ Macinnes, Duncan A. (1939). The principles of electrochemistry. Reinnhold Publishing Corporation. pp. 447-451.
  10. ^ "Martin (John) M. Atalla". National Inventors Hall of Fame. 2009. Retrieved 2013.
  11. ^ a b "Dawon Kahng". National Inventors Hall of Fame. Retrieved 2019.
  12. ^ Lojek, Bo (2007). History of Semiconductor Engineering. Springer Science & Business Media. pp. 120 & 321-323. ISBN 9783540342588.
  13. ^ a b Bassett, Ross Knox (2007). To the Digital Age: Research Labs, Start-up Companies, and the Rise of MOS Technology. Johns Hopkins University Press. p. 46. ISBN 9780801886393.
  14. ^ Aluminum Passivation [1]
  15. ^ Chemical Conversion Coating on Aluminum [2]
  16. ^ Aluminum Anodizing Process [3]
  17. ^ "Stainless Steel Passivation". Arrow Cryogenics. Retrieved 2014.
  18. ^
  19. ^
  20. ^ a b
  21. ^ "Archived copy" (PDF). Archived from the original (PDF) on 12 September 2012. Retrieved 2013.CS1 maint: Archived copy as title (link)

Further reading

  This article uses material from the Wikipedia page available here. It is released under the Creative Commons Attribution-Share-Alike License 3.0.



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