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Phosphate coatings corrosion resistance

Pure lead has low creep and fatigue resistance, but its physical properties can be improved by the addition of small amounts of silver, copper, antimony, or tellurium. Lead-clad equipment is in common use in many chemical plants. The excellent corrosion-resistance properties of lead are caused by the formation of protective surface coatings. If the coating is one of the highly insoluble lead salts, such as sulfate, carbonate, or phosphate, good corrosion resistance is obtained. Little protection is offered, however, if the coating is a soluble salt, such as nitrate, acetate, or chloride. As a result, lead shows good resistance to sufuric acid and phosphoric acid, but it is susceptible to attack by acetic acid and nitric acid. [Pg.432]

Dichromates and chromic acid are used as sealers or after-dips to improve the corrosion resistance of various coatings on metals. Eor example, phosphate coatings on galvani2ed iron or steel as well as sulfuric acid anodic coatings on aluminum can be sealed by hexavalent chromium baths. [Pg.143]

This is the final neutralizing rinse after the pre-treatment to obtain a better corrosion resistance. The phosphated surfaces are treated with chromic acid-based or acidified sodium dichromate solutions which are not affected by moisture and thus protect the phosphate coating. [Pg.404]

Chlorinated rubber is extensively employed in industrial corrosion-resistant surface coatings, for which purpose it is marketed by ICI under the trade name Alloprene. Although thermoplastic moulding compositions have been made by plasticising with the common ester plasticisers such as tritolyl phosphate they are of no commercial importance. [Pg.865]

The majority of phosphate processes in use today are accelerated to obtain shorter treatment times and lower processing temperatures. The most common mode of acceleration is by the addition of oxidising agents such as nitrate, nitrite, chlorate and hydrogen peroxide. By this means, a processing time of 1 to 5 min can be obtained at temperatures of 43-71 °C. The resultant coatings are much smoother and thinner than those from unaccelerated processes, and, while the corrosion resistance is lower, they cause less reduction of paint gloss and are more suited to mass-production requirements. [Pg.709]

Znj(P04)2 4H2 0 appears in three crystal forms, a-hopeite (rhombic plates), 3-hopeite (rhombic crystals), and p-hopeite (triclinic crystals). Their transition points are at 105, 140 and 163°C respectively. It has been observed that zinc phosphate coatings heated in the absence of air lose their corrosion resistance at between 150 and 163°C. [Pg.711]

Manganese phosphate coatings heated in the absence of air lose their corrosion resistance at between 200 and 218°C. At these temperatures, between 75 and 80% of the water of hydration is lost and it is assumed that this results in a volume decrease of the coating which causes voids and thereby lowers the corrosion resistance. Fig. 15.4 shows the loss of water of hydration from zinc, iron and iron-manganese phosphate coatings. [Pg.711]

Heavy phosphate coatings do not necessarily have better corrosion resistance than lighter coatings. Even with a single process, e.g. zinc/iron/ phosphate/nitrate, no consistent relationship has been found between corrosion resistance and either coating weight or weight of metal dissolved. [Pg.715]

Conversion coating Conversion coatings are chemical solutions which react with the metal surface to create a corrosion-resistant layer onto which the coating can bond. For mild steel iron phosphate is used to attain good adhesion, but it does not give the underfilm corrosion resistance which can be obtained using zinc phosphate. Zinc coatings can be treated with either zinc phosphate or chromate. Aluminium is usually treated with chromate... [Pg.746]

Our electrochemical work differed drastically from the Groseclose work in that polymer coated metal samples were employed. Furthermore, we found that coatings can have corrosion resistance when their rest potentials are either more noble (B210/NVP) or less noble (B210/GBL) than the uncoated substrate. Leidheiser (22,23) examin zinc phosphate pretreated panels with automotive primer after 10 days exposure to the salt spray. The start and finish rest potentials of the samples with good paint performance were consistently more negative than those samples with poor paint performance ... [Pg.55]

The "Mannich" adduct synthesized from the condensation of formaldehyde, 2-(methylamino)ethanol and poly-4-vinylphenol as shown in Structure I, has been evaluated as a function of molecular weight versus corrosion resistance as measured by salt spray and humidity tests on Bonderite 1000, an iron phosphate conversion coating. The molecular weight of the polymer was varied from approximately = 2,900 to 60,000. The corrosion resistance results were essentially equivalent over the molecular weight range evaluated. [Pg.209]


See other pages where Phosphate coatings corrosion resistance is mentioned: [Pg.528]    [Pg.222]    [Pg.223]    [Pg.462]    [Pg.330]    [Pg.353]    [Pg.403]    [Pg.199]    [Pg.989]    [Pg.520]    [Pg.52]    [Pg.456]    [Pg.623]    [Pg.706]    [Pg.708]    [Pg.710]    [Pg.710]    [Pg.710]    [Pg.711]    [Pg.714]    [Pg.715]    [Pg.716]    [Pg.716]    [Pg.716]    [Pg.718]    [Pg.719]    [Pg.719]    [Pg.720]    [Pg.13]    [Pg.263]    [Pg.84]    [Pg.227]    [Pg.205]    [Pg.205]    [Pg.47]    [Pg.435]   
See also in sourсe #XX -- [ Pg.15 , Pg.30 ]

See also in sourсe #XX -- [ Pg.15 , Pg.30 ]




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Coating, resist

Coatings corrosion resistance

Coatings corrosion-resistant

Coatings resistant

Corrosion resistance

Phosphatic coatings

Phosphating coatings

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