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・ Phosphoglycerate
・ Phosphoglycerate dehydrogenase
・ Phosphoglycerate kinase
・ Phosphoglycerate kinase (GTP)
・ Phosphoglycerate mutase
・ Phosphoglycerate phosphatase
・ Phosphoglyceric acid
・ Phosphoglycerol geranylgeranyltransferase
・ Phosphamidon
・ Phosphatase
・ Phosphate
・ Phosphate acetyltransferase
・ Phosphate Beds
・ Phosphate binder
・ Phosphate butyryltransferase
Phosphate conversion coating
・ Phosphate glass
・ Phosphate Hill Power Station
・ Phosphate minerals
・ Phosphate mining in Nauru
・ Phosphate nephropathy
・ Phosphate rich organic manure
・ Phosphate soda
・ Phosphate solubilizing bacteria
・ Phosphate test
・ Phosphate-buffered saline
・ Phosphate-selective porin
・ Phosphate-transporting ATPase
・ Phosphated distarch phosphate
・ Phosphatherium


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Phosphate conversion coating : ウィキペディア英語版
Phosphate conversion coating

Phosphate coatings are used on steel parts for corrosion resistance, lubricity, or as a foundation for subsequent coatings or painting. It serves as a conversion coating in which a dilute solution of phosphoric acid and phosphate salts is applied via spraying or immersion and chemically reacts with the surface of the part being coated to form a layer of insoluble, crystalline phosphates.
Phosphate conversion coatings can also be used on aluminium, zinc, cadmium, silver and tin.
The main types of phosphate coatings are manganese, iron and zinc. Manganese phosphates are used both for corrosion resistance and lubricity and are applied only by immersion. Iron phosphates are typically used as a base for further coatings or painting and are applied by immersion or by spraying. Zinc phosphates are used for corrosion resistance (phosphate and oil), a lubricant base layer, and as a paint/coating base and can also be applied by immersion or spraying.〔〔
==Process==
The application of phosphate coatings makes use of phosphoric acid and takes advantage of the low solubility of phosphates in medium or high pH solutions. Iron, zinc or manganese phosphate salts are dissolved in a solution of phosphoric acid. When steel or iron parts are placed in the phosphoric acid, a classic acid and metal reaction takes place which locally depletes the hydronium (H3O+) ions, raising the pH, and causing the dissolved salt to fall out of solution and be precipitated on the surface. The acid and metal reaction also creates iron phosphate locally which may also be deposited. In the case of depositing zinc phosphate or manganese phosphate the additional iron phosphate is frequently an undesirable addition to the coating.
The acid and metal reaction also generates hydrogen gas in the form of tiny bubbles that adhere to the surface of the metal. These prevent the acid from reaching the metal surface and slows down the reaction. To overcome this sodium nitrite is frequently added to act as an oxidizing agent that reacts with the hydrogen to form water. This chemistry is known as a nitrate accelerated solution. Hydrogen is prevented from forming a passivating layer on the surface by the oxidant additive.〔
The following is a typical phosphating procedure:〔
#cleaning the surface
#rinsing
#surface activation
#phosphating
#rinsing
#neutralizing rinse (optional)
#drying
#application of supplemental coatings: lubricants, sealers, oil, etc.
The performance of the phosphate coating is significantly dependent on the crystal structure as well as the weight. For example, a microcrystalline structure is usually optimal for corrosion resistance or subsequent painting. A coarse grain structure impregnated with oil, however, may be the most desirable for wear resistance. These factors are controlled by selecting the appropriate phosphate solution, using various additives, and controlling bath temperature, concentration, and phosphating time.〔 A widely used additive is to seed the metal surface with tiny particles of titanium salts by adding these to the rinse bath preceding the phosphating.〔 This is known as activation.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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