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Zinc Phosphating—Immersion

Granodixing Process, developed by the American Chemical Paint Co, Waterbury, Conn for rust prevention of iron, steel, zinc or cadmium consists in immersing the material in a hot soln of acid zinc phosphate. This operation forms an acid resistant coating. The resulting material may be painted... [Pg.766]

All of the coating was carried out on 3 inch X 5 inch, 24-gage zinc-phosphated (Bonderite EP-2), cold rolled steel panels with a deionized rinse. Each panel was immersed in the electrodeposition bath to a constant depth of 10 cm so that a current density or 2.0 ma/cm2 could be used for all coating experiments. [Pg.172]

Phosphating A steel object is immersed in a bath containing zinc phosphate and phosphoric acid to precipitate zinc phosphate on the surface. [Pg.436]

The tissue blocks were immersed in 0.1 M phosphate buffer containing 2% glutaraldehyde and 5% sucrose (pH 7.4). The tissue blocks were immersed in ZIO solution. The ZIO solution was prepared as follows 3 g of zinc (powder) was dissolved ultrasonically in 20 mL distilled water and 1 g of iodine crystals was slowly added to the zinc suspension with stirring. After cooling, 4 mL of the filtered solution was mixed with 2 mL of Tris-HCl buffer (pH 7.5) and 2 mL of 2% Os04 solution. Treatment with this ZIO mixture was carried out for 16-20 h at 4°C in the dark. [Pg.241]

One of the best finishes for firearm steel is phosphatizing (Parkerizing) but few manufacturers offer this finish other than if required for military or police markets. The process deposits a crystalline layer of phosphates on the metal surface by immersion in a bath of iron, zinc, or manganese dioxide and phosphoric acid. Of these, a manganese phosphate finish is preferred for military use. [Pg.100]

Phosphating provides a corrosion-resistant undercoat for paint finishes on steel (particularly automotive bodies), and to a lesser extent on zinc and aluminium. The usual process consists of immersion in a bath containing phosphoric acid, a metal phosphate (usually iron or zinc), and an accelerator, the pH varying between 1.8 and 3.2, at 60-90°C. [Pg.364]

It is also used for the manufacture of soluble phosphate fertilizers (Chap. 21), of ammonium sulfate for use as a fertilizer, of other sulfates, and in the manufacture of many chemicals and drugs. Steel is usually cleaned of iron rust (is pickled ) by immersion in a bath of sulfuric acid before it is coated with zinc, tin, or enamel. The use of sulfuric acid as the electrolyte in ordinary storage cells has been mentioned (Chap. 14). [Pg.372]

Addition of compounds with appropriate functionality to serve as nucleation sites for calcium phosphate growth to polymers can potentially improve the biocompatibility of the latter and thus the long-term stability of implant devices (Drelich and Field, 2007). Zinc stearate was added to poly(ethylene) to form poly(ethylene)-stearate blends with increased surface porosity potentially able to improve mechanical stability of the implant through enhanced osseointegration, improved rates and quality of bone-implant fusion and enhanced soft tissue wound healing via stimulation of angiogenesis. While immersion of these blends in supersaturated calcium phosphate solutions triggered deposition of a porous layer, the deposition rate was very slow, around 100 nm/day. [Pg.130]

Figure 10a. SEM photomicrograph of copper-2% zinc alloy exposed for 4 h in 11.6 g/L y-globulin phosphated saline solution at 25°, pH 7.4, by immersion only. Figure 10a. SEM photomicrograph of copper-2% zinc alloy exposed for 4 h in 11.6 g/L y-globulin phosphated saline solution at 25°, pH 7.4, by immersion only.
Figures 12a-d present the surface appearances of copper-2% zinc alloy exposed to the phosphated-saline albumin-globulin-fibrinogen solution. The as-immersed surface (Figures 12a-b) exhibited a protein layer, protein accumulation, and copper chloride phosphates as corrosion products. Polarization at —0.3 V eliminated the outer surfaces of protein accumulation and of corrosion products. Only the underlying protein layer was observed (Figure 11c). Polarization at -0.5 V desorbed most of the protein (Figure lid). Figures 12a-d present the surface appearances of copper-2% zinc alloy exposed to the phosphated-saline albumin-globulin-fibrinogen solution. The as-immersed surface (Figures 12a-b) exhibited a protein layer, protein accumulation, and copper chloride phosphates as corrosion products. Polarization at —0.3 V eliminated the outer surfaces of protein accumulation and of corrosion products. Only the underlying protein layer was observed (Figure 11c). Polarization at -0.5 V desorbed most of the protein (Figure lid).

See other pages where Zinc Phosphating—Immersion is mentioned: [Pg.223]    [Pg.520]    [Pg.717]    [Pg.335]    [Pg.263]    [Pg.151]    [Pg.182]    [Pg.187]    [Pg.435]    [Pg.583]    [Pg.284]    [Pg.520]    [Pg.408]    [Pg.746]    [Pg.461]    [Pg.417]    [Pg.144]    [Pg.96]    [Pg.471]    [Pg.389]    [Pg.376]    [Pg.126]    [Pg.456]    [Pg.706]    [Pg.252]    [Pg.699]    [Pg.187]    [Pg.699]    [Pg.435]    [Pg.326]    [Pg.302]    [Pg.413]    [Pg.413]    [Pg.421]    [Pg.426]    [Pg.126]   


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