Nitrogen passive forms

Nitric acid reacts with all metals except gold, iridium, platinum, rhodium, tantalum, titanium, and certain alloys. It reacts violentiy with sodium and potassium to produce nitrogen. Most metals are converted iato nitrates arsenic, antimony, and tin form oxides. Chrome, iron, and aluminum readily dissolve ia dilute nitric acid but with concentrated acid form a metal oxide layer that passivates the metal, ie, prevents further reaction. 

Phosphorus oxynitride, PON, is a useful starting product, as a phosphorus and nitrogen source, to prepare various nitridooxophos-phates, in particular phosphorus oxynitride glass compositions (211). Moreover, it shows as a material excellent chemical stability with potential applications in several domains. In microelectronics, for example, PON has been used to form by evaporation insulating films for the passivation of III-V InP substrates and the elaboration of MIS (metal-insulator-semiconductor) structures (190, 212-215). PON could have also valuable properties in flame retardancy (176,191,216). 

Curing is first performed at 200 C in air and then at 350 C in a nitrogen atmosphere. Through-holes are etched using a negative photoresist as the etching mask and an etchant containing hydrazine hydrate and ethylenediamine. Next, the second level metallization is formed. PIQ film is then formed on the second level metallization. This acts as a passivation film. 

The purer forms of iron (wrought iron and steel) appear to be much more susceptible to this kind of reaction than cast iron.3 If the attacking acid is readily reducible by hydrogen, many secondary reactions may take place. Thus with nitric acid, oxides of nitrogen and ammonia may be evolved, whilst with selenic acid a deposit of elementary selenium is obtained (see below). When iron is exposed to the action of acids that are also powerful oxidisers—such as, for example, fairly concentrated solutions of nitric and chromic acids,—it is frequently rendered inert or passive.4 Its surface may remain perfectly bright, but the metal does not show any appreciable solution in the acid, and if removed and immersed in dilute solutions of such salts as copper and silver sulphates, no reaction takes place, although ordinary active iron would cause an immediate precipitation of the more electronegative metal. 

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