Lead dross

Blei, n. lead, -abgang, m. lead dross, lead scoria, -ablagerung,/. lead deposit, -acetat, n. lead acetate, -ader, /. lead vein, -anti-monerz, n., -antimonglanz, m. zinkenite. -arbeit, /. lead smelting plumbing, -arse-nat, n. lead arsenate, -arsenglanz, m. sarto-rite. -arsenik, m. lead arsenate lead arsenide, -art, /. kind or variety of lead. 

Blei-asche, /. lead dross lead ash the gray film of oxide on lead exposed to air. -aus-kleidung, /. lead lining. -azetat, n. lead acetate, -bad, n. lead bath, -bauzn, m. lead tree, arbor aaturni. 

SYNS ANGLISLITE O BLEISULFAT (GERMAN) C.I. 77630 C.I. PIGMENT WHITE 3 O FAST WTIITE FREEMANS WHITE LEAD LEAD BOTTOMS LEAD DROSS (DOT) LEAD SULFATE, solid, containing more than 3% free acid (DOT) MILK WHITE MULHOUSE WHITE SULFATE de PLOMB (FRENCH) SULFURIC ACID, LEAD(2+) SALT (1 1)... 

ETHYLENEDINITRILOTETRACETATE see LDBOOO LEAD DROSS see LDCOOO LEAD DROSS (DOT) see LDYOOO LEAD (2-),... 

Lead dross from heating lead ore (principally lead sulphide) in an oxidizing environment is high in lead sulphate. In fact, this process is one of the methods used commercially to manufacture this acid. 

Similarly, finely divided mixed metals undergo electrochemical reactions in contact with one another, sometimes with sufficient heat to ignite surrounding combustible materials or with a dangerous depletion of surrounding oxygen in confined spaces, o Lead dross (mostly lead sulphate) is acidic, o Arsenical flue dust and other metal by-products are toxic, o Residues may be mixed with other compounds and metals such as lead, cadmium, mercury, and uranium. 

Slag and bullion are tapped from the furnace hearth into a forehearth where they are separated. Slag flows from the forehearth into a granulation launder and lead bullion flows to a lead kettle of around 100 tonnes capacity either directly or via batch ladles. The bullion is allowed to cool in the kettle to separate a copper-lead dross, reducing the copper content to around 0.2 per cent. The resulting lead bullion is then cast into blocks of up to four tonnes each for transfer or sale to a lead refinery. 

The bismuth dross formed is removed from the surface of the lead on completion of the batch. Drosses normally contain between three and ten per cent Bi, and commonly around six per cent Calcium plus magnesium total around two per cent and the remainder is lead. Drosses can be upgraded by pressing or centrifuging to remove entrained lead. 

The lead is supplied by the metallurgical works in the form of pigs of about 99.8 per cent purity from the melting kettle it is fed directly to the container. Scr ip lead is often added to the lead bath in order to reduce the price of the pipes. Pure lead gives aboud 2% lead dross, whereas about 8% residue have to be taken into account in scrap lead. The dross is collected and refined by chemical works. Larger quantities of scrap lead are refined in a simple manner by heating it to a temperature of about 450 to 500 °C and skimming off the dross from the surface of the metal. 

Lead is usually processed from ore to refined metal in four stages. These are ore dressing, smelting, drossing, and refining (see Mineral recovery and processing). 

The furnace charge consists of 2iac—lead siater, metallurgical coke, and recirculating metallic drosses and flux. The charge cycle is fully automatic. Hoist... 

The lead and 2inc are separated into two molten phases by progressive cooling. Following ammonium chloride treatment to remove dross, the lead is returned to the condenser. Zinc is cast into ingots after dissolved lead is removed by cooling. 

Dressing. The impure lead bulhon, produced from any of the smelting processes, is cooled to remove dissolved copper prior to the refining operation. The operation is referred to as copper drossing, and is performed in one or two 250 t cast-iron ketdes. The process consists of skimming off the dross, stirring the lead, and reskimming. 

Stirrer is then stopped, and the lead skimmed. The dross should contain from 0.004 to 0.04% copper. 

The dross from this operation contains considerable quantities of copper and lead as well as other valuable metals. Separation and recovery is economically imperative. The dross is treated to produce readily separated stratified layers of slag, speiss, matte, and lead. Two processes are primarily used. 

The success of the process results from the fact that nowhere inside the furnace is heat extracted from the copper-saturated blast furnace buUion through a soUd surface. The problem of accretion formation (metal buUd-up), which has plagued many other attempts to estabUsh a copper dtossing operation of this type, does not arise. In the cooling launder, lead-rich matte and slag accumulate on the water-cooled plates, but these ate designed so that when they ate lifted from the buUion stream, the dross cracks off and is swept into the furnace via the cooled lead pot. 

Soda. Process. Use of a soda smelting process for treating copper drosses in the reverberatory furnace increases the copper to lead ratios in the matte and speiss, and aUows lower operating temperatures. A flow sheet describing this process is shown in Figure 11. 

In the fumace/ketde batch process, a charge of drossed blast furnace buUion is treated in a reverberatory furnace or a kettie (see Fig. 12). Oxygen is supphed in the form of compressed air or as lead oxide blown into the bath through submerged pipes. The formation of lead oxide serves by mass action to assure the removal of the impurities to the desired low concentrations. The softening reactions are... 

The continuous softening process used by The Broken Hill Associated Smelters Pty., Ltd. is particularly suitable for lead buUion of fairly uniform impurity content. The copper-drossed blast furnace buUion continuously flows in the feed end of a reverberatory furnace at 420°C, and the softened lead leaves the opposite end at 750°C. Oxidation and agitation is provided by compressed air blown through pipes extending down through the arch of the furnace into the bath. 

The dezincing chamber is set first in the drossed lead bath, then water connections are immediately made in order to prevent the formation of steam within the water jacket. While the temperature is being raised, the vacuum pump is placed in operation and the agitator started. The temperature is then raised to 600°C and held throughout the operation. 

In the Betterton-KroU process the dezinced lead is pumped to the debismuthizing kettie, in which special care is taken to remove drosses that wastefuUy consume the calcium and magnesium. The skimmed blocks from the previous debismuthizing kettie are added to the bath at 420°C and stirred for a short time to enrich the dross with the bismuth being extracted from the new charge. This enriched dross is skimmed to blocks and sent to the bismuth recovery plant. 

FoUowing the removal of the enriched dross, the required quantities of calcium, as a lead—calcium alloy and magnesium in the form of metal ingots, are added. The bath is stirred about 30 min to incorporate the reagents and hasten the reaction. The molten lead is cooled gradually to 380°C to permit the precipitate to grow and soHdify. The dross is skimmed for use with the next lot of lead to be treated. 

The lead contains residual calcium and magnesium that must be removed by chlorination or treatment with caustic and niter. The molten lead is pumped or laundered to the casting kettles in which it is again treated with caustic and niter prior to mol ding, After a final drossing, the refined lead is cast into 45-kg pigs or 1- and 2-t blocks. 

Lead and its alloys are generally melted, handled, and refined in cast-iron, cast-steel, welded-steel, or spun-steel melting ketdes without fear of contamination by iron (qv). Normal melting procedures require no dux cover for lead. Special reactive metal alloys require special alloying elements, duxes, or covers to prevent dross formation and loss of the alloying elements. 

Lead alloys containing 0.09—0.15 wt % calcium and 0.015—0.03 wt % aluminum are used for the negative battery grids of virtually all lead—acid batteries in the United States and are also used in Japan, Canada, and Europe. If the molten alloy is held at too low a temperature, the aluminum precipitates from solution, rises to the surface of the molten alloy as finely divided aluminum particles, and enters the dross layer atop the melt. 

Lead—antimony or lead—arsenic ahoys must not be mixed with lead—calcium (aluminum) ahoys in the molten state. Addition of lead—calcium—aluminum ahoys to lead—antimony ahoys results in reaction of calcium or aluminum with the antimony and arsenic to form arsenides and antimonides. The dross containing the arsenides and antimonides floats to the surface of the molten lead ahoy and may generate poisonous arsine or stibine if it becomes wet. Care must be taken to prevent mixing of calcium and antimony ahoys and to ensure proper handling of drosses. 

If the temperature of a molten lead—calcium (tin)—aluminum ahoy is not kept sufficiently high, finely divided aluminum particles may precipitate and float to the top of the melt. These may become mixed with oxides of lead in the dross. The finely divided aluminum particles can react violently with the oxides in the dross if ignited. Ignition can occur if attempts are made to melt or bum the dross away from areas of buildup with a torch. The oxides in the dross can supply oxygen for the combustion of aluminum once ignited. 

Precipita.tlon, In the simplest case, the solubihty of an impurity in the Hquid metal changes with temperature. Thus the impurity may precipitate as a sohd phase upon cooling. For instance, the removal of iron from tin and of copper from lead are achieved by precipitation. When the soHd is lighter than the Hquid, it floats as a dross on the surface of the melt where it is easily removed by scraping. The process is called dressing. 

Precipitation can also occur upon chemical reaction between the impurity and a precipitating agent to form a compound insoluble in the molten metal. The refining of cmde lead is an example of this process. Most copper is removed as a copper dross upon cooling of the molten metal, but the removal of the residual copper is achieved by adding sulfur to precipitate copper sulfide. The precious metals are separated by adding zinc to Hquid lead to form soHd intermetaHic compounds of zinc with gold and silver (Parkes process). The precious metals can then be recovered by further treatment (see Lead). 

---