Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Corrosion protective oxide coating

Aluminum containers are recommended for many appHcations because of the very hard, corrosion-resistant oxide coating. They are deficient in only one respect once the protective skin has been penetrated, aluminum corrosion accelerates. [Pg.349]

Hafnium is a ductile metal that looks and feels much hke stainless steel, but it is significantly heavier than steel. When freshly cut, metallic hafnium has a bright silvery shine. When the fresh surface is exposed to air, it rapidly forms a protective oxidized coating on its surface. Therefore, once oxidized, hafnium resists corrosion, as do most transition metals, when exposed to the air. Chemically and physically, hafnium is very similar to zirconium, which is located just above it in group 4 on the periodic table. In fact, they are so similar that it is almost impossible to secure a pure sample of either one without a small percentage of the other. Each will contain a small amount of the other metal after final refining. [Pg.149]

The chemical resistance of aluminum is fair, but any chemical which destroys the protective oxide coating will lead to rapid corrosion therefore, strong acids, alkalies, and mercury must be kept out of contact with aluminum. [Pg.311]

Iron can also form a protective oxide coating. This coating is not an infallible shield against corrosion, however when steel is exposed to oxygen in moist air, the oxide that forms tends to scale off, exposing new metal surfaces to corrosion. [Pg.486]

Currently, tin is used mainly as a protective coating for steel, especially for cans used as food containers. The thin layer of tin, applied electrolytically, forms a protective oxide coating that prevents further corrosion. [Pg.882]

The controlled grain structure allows forming an adherent protective oxide coating within days when placed in an electrowinning cell without the necessity of being preconditioned [13]. In sulfuric acid electrolytes, the introduction of cobalt ions into the solution reduces the anode overvoltage and the corrosion rate of lead. [Pg.186]

Vomiting Agents are generally slow to decompose in water. Some agents are self-protecting and form a protective oxide coating that delays further hydrolysis. Agents may be corrosive to some metals. [Pg.102]

CORROSION, FRETTING - A type of corrosion which occurs where metals slide over each other. Long tubes in heat exchangers often vibrate, causing metal to metal contact, tube supports etc.. The metal to metal rubbing causes mechanical damage to the protective oxide coating. [Pg.49]

Corrosion involves the oxidation of metals to form mainly oxides and sulfides. Some metals, such as aluminum, form a thin protective oxide coating that inhibits their further corrosion. Corrosion of iron can be prevented by a coating (such as paint), by alloying, and by cathodic protection. [Pg.607]

The corrosion of aluminium alloys in high purity water is complex and many of the factors responsible for this corrosion are interrelated. In high purity, deionized water, general thinning of the cladding caused by uniform corrosion is very low. The fuel enters the basin with, in some cases, several millimetres of protective oxide coating formed at high temperatures. When corrosion by water... [Pg.40]

Finally, the stainless-steel bipolar plate consists of a separator and current collectors. The plate is exposed to the anodic environment on one side and the cathodic environment on the other. The low oxygen partial pressure on the anodic side of the bipolar plate prevents the formation of a protective oxide coating and, on the cathode side, the contact electrical resistance increases as an oxide scale builds up. Active research is focused on finding alloys for bipolar current-collector materials that function well in both anodic and cathodic environments, have a low cost and ohmic resistance, and have good corrosion resistance [15]. [Pg.71]

Dust and other pollutants may collect in rain sheltered positions and accelerate corrosion by disturbing the formation of a protective oxide coating. These rain-sheltered areas will often show staining as a result of the corrosion. When possible, such rain sheltered areas should be eliminated during the design stage. [Pg.60]

To prevent compromising the integrity of the protective oxide coating on stainless steel, only soft-bristle brushes should be used in cases where scrubbing is required. Once stainless steel surfaces are scratched, these rapidly become susceptible to oxidation and corrosion. As such, fiber or metal scratch pads or brushes should never be used for removal of tenacious deposits. [Pg.142]


See other pages where Corrosion protective oxide coating is mentioned: [Pg.184]    [Pg.436]    [Pg.791]    [Pg.696]    [Pg.183]    [Pg.488]    [Pg.193]    [Pg.290]    [Pg.59]    [Pg.175]    [Pg.498]    [Pg.589]    [Pg.384]    [Pg.160]    [Pg.41]    [Pg.56]    [Pg.86]    [Pg.165]    [Pg.600]   
See also in sourсe #XX -- [ Pg.486 ]




SEARCH



Coating corrosion protection coatings

Coating protection

Corrosion protection coatings

Corrosion, Protective Coatings

Oxide coating

Oxides Corrosion

Oxidic coatings

Protective coatings

Protective oxidation

Protective oxides

© 2024 chempedia.info