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Zinc by immersion

Galvanizing—the method of coating iron or steel with zinc by immersion of the metal in a bath of molten zinc. [Pg.48]

The same method is given in BS 903 Part A3782 which also contains a national annex giving a second method for assessing the degree of corrosion when the rubber is not in contact with the metal. Zinc is used as the standard metal as this is fairly readily corroded. A strip of zinc and the rubber test piece are both suspended over distilled water in a stoppered container maintained at 50°C. After a period of three weeks, the corrosion products are removed from the zinc by immersion in chromium trioxide solution and the loss in weight used as the measure of degree of corrosion. This is a very sensitive method but even more care has to be taken than in the contact method to avoid contamination and to obtain reproducible results. [Pg.376]

Galvanize gal-v9- nlz (1802) v. To coat iron or steel with zinc by immersing in molten zinc to produce a coating of zinc-iron alloy. [Pg.448]

This conversion is normally accompHshed by immersion, but spraying, swabbing, bmshing, and electrolytic methods are also employed (178) (see Metal SURFACE treatments). The metals that benefit from chromium surface conversion are aluminum, cadmium, copper, magnesium, silver, and 2inc. Zinc is the largest consumer of chromium conversion baths, and more formulations are developed for 2inc than for any other metal. [Pg.143]

Experiments in which rolled high-grade zinc was immersed in distilled water for 15 days at various temperatures are described by Cox . The figures which he obtained are given in Table 4.36. [Pg.820]

Galvanising baths are generally constructed from special mild steel boiler plate having very small amounts of trace elements so that they are not rapidly attacked by molten zinc but they can be made of ceramic materials and heated from the top or by immersion heaters. [Pg.388]

Consequentiy, a zinc coating oxidizes preferentiaiiy and protects steel from corrosion. Zinc coatings are applied in severai ways by immersion in moiten zinc, by paint containing powdered zinc, or by electroplating. [Pg.1478]

For example, consider a system in which metallic zinc is immersed in a solution of copper(II) ions. Copper in the solution is replaced by zinc which is dissolved and metallic copper is deposited on the zinc. The entire change of enthalpy in this process is converted to heat. If, however, this reaction is carried out by immersing a zinc rod into a solution of zinc ions and a copper rod into a solution of copper ions and the solutions are brought into contact (e.g. across a porous diaphragm, to prevent mixing), then zinc will pass into the solution of zinc ions and copper will be deposited from the solution of copper ions only when both metals are connected externally by a conductor so that there is a closed circuit. The cell can then carry out work in the external part of the circuit. In the first arrangement, reversible reaction is impossible but it becomes possible in the second, provided that the other conditions for reversibility are fulfilled. [Pg.169]

Hot dip coating is the process of coating a metallic workpiece with another metal by immersion in a molten bath to provide a protective him. Galvanizing (hot dip zinc) is the most common hot dip coating. [Pg.347]

The amount of zinc in the soil was determined by immersing a rod of clean, pure zinc in the solution of zinc sulfate plus sulfuric acicf and measuring Ez 2+ z,i as —0.864 V. What is the concentration of the zinc solution formed by digesting in acid and what is the activity of the zinc salt In order to answer there questions, we will need to know the standard electrode potential, n —0.760 V. [Pg.51]

C. N-Hydroxy-4-(p-chlorophenyl)thiazole-2(3H)-thione. O-Ethyl S-[2-oximino-2-(p-chlorophenyl)ethyl]dithiocarbonate (56.0 g, 0.19 mol) is placed in a 500-mL round-bottomed flask that is equipped with a magnetic stir bar. Diethyl ether (120 mL) is added and the slurry is treated at 0°C in small portions with solid anhydrous zinc chloride, ZnClj, 79.1 g, 0.58 mol) at such a rate that the solvent does not boil constantly (Note 8). After the addition is complete, the flask is stoppered with a drying tube (CaCl2) and stirring is continued for 48 hr at 20°C. The reaction mixture turns into a dear, dark brown solution that solidifies toward the end of the reaction. The flask is immersed in an ice bath and treated dropwise with 5.5 M hydrochloric add (140 mL, Note 9). The precipitate dissolves immediately. Stirring is continued for 30 min at 0°C whereupon a tan-colored solid separates. This material is collected by filtration. It is washed with small portions of diethyl ether (total of 110 mL) and dried to afford 39.8 g (86%) of N-hydroxy-4-(p-chlorophenyl)thiazole-2(3H)-thione (Note 10). The crude material is transferred to a 2-L, round-bottomed flask equipped with a reflux condenser. 2-Propanol (760 mL) is added and the reaction mixture is heated to reflux. Once a dear solution is obtained the heat source is immediately removed (Note 11). The solution is allowed to cool to room temperature. Precipitation of N-hydroxy-4-(p-chlorophenyl)thiazole-2(3H)-thione is completed by immersing the flask for 30 min in an acetone-dry ice bath (-78°C). The product is collected by filtration and dried to afford 21.9 g (53.5%) of N-hydroxy-4-(p-chlorophenyl)thiazole-2(3H)-thione as tan crystals (Notes 12,13). [Pg.116]

Preparation of Zinc.—To obtain perfectly pure zinc is a task of some difficulty, so much so that the commercial article is never met with in a puro state, hut rather with variable quantities of arsenic, cadmium, tin, lead, manganese, iron, cobalt, and nickel. In order to obtain perfectly pure metal, the purest commercial ziuo should be dissolved in dilute sulphuric acid, filtered from any residue, and the foreign metals thrown down by Immersing plates of zinc in the liquid till no further deposit takes place. After separating the precipitated metals, which may be tin, lead, copper, cadmium, antimony, and a trace of arsenic, the solution is treated with carbonate of soda, and the carbonate of zinc, which Falls after filtration and thorough washing, Is dried, heated to redness to expel carbonic acid, mixed with charcoal or lampblack, and introduced into a crucible as represented in Fig. 23, placed in a furnace,... [Pg.1154]

The historically important Daniell cell consists of a copper vessel containing a saturated solution of copper sulphate which forms one of the two electrode systems, and a central amalgamated zinc rod immersed in a zinc sulphate/sulphuric acid solution, which forms the other (Fig. 2.3). Gross mixing of the two solutions is prevented by a membrane or porous pot. It is assumed here that both electrodes are provided with copper terminals. [Pg.23]

In hoi galvanizing, zinc is applied to iron and steel parts by immersing the parts into u butli of triollen zinc Whereas in principle almost any metal could be coaled with molten zinc, this coating serves no worthwhile purpose on most metals. The combination of zinc and ferrous materials are almost uniquely suited to each other. Aluminum and cadmium are the only other similar combinations, Zinc provides iron parts with better corrosion protection by developing a coating of zinc and zinc compounds on the base metal surface. [Pg.983]

One may construct a Daniell cell quite simply by immersing a strip of zinc metal in an aqueous solution of zinc sulfate contained in a porous... [Pg.532]


See other pages where Zinc by immersion is mentioned: [Pg.152]    [Pg.288]    [Pg.195]    [Pg.152]    [Pg.288]    [Pg.195]    [Pg.335]    [Pg.130]    [Pg.223]    [Pg.285]    [Pg.100]    [Pg.234]    [Pg.85]    [Pg.818]    [Pg.351]    [Pg.501]    [Pg.706]    [Pg.717]    [Pg.742]    [Pg.118]    [Pg.210]    [Pg.335]    [Pg.699]    [Pg.506]    [Pg.140]    [Pg.99]    [Pg.699]    [Pg.230]    [Pg.292]    [Pg.364]    [Pg.435]    [Pg.181]    [Pg.317]    [Pg.80]   
See also in sourсe #XX -- [ Pg.133 ]




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