Antimonial lead

Rotar Furnace. The rotary furnace, which has more flexibiUty than either the blast or reverberatory furnace, can produce either a single metal product or a high and a low antimonial alloy. The rotary furnace, like the reverberatory furnace, allows for the option of producing low antimony lead for further refinement. 

Automobile battery grids employ about 1—3 wt % antimony—lead alloys. Hybrid batteries use low (1.6—2.5 wt %) alloys for the positive grids and nonantimony alloys for the negative grids to give reduced or no water loss. The posts and straps of virtually all lead—acid batteries are made of alloys containing about 3 wt % antimony. 

Selenium acts as a grain refiner in lead antimony alloys (114,115). The addition of 0.02% Se to a 2.5% antimonial lead alloy yields a sound casting having a fine-grain stmcture. Battery grids produced from this alloy permit the manufacture of low maintenance and maintenance-free lead—acid batteries with an insignificant loss of electrolyte and good performance stability. 

By-Product and Secondary Antimony. Antimony is often found associated with lead ores. The smelting and refining of these ores yield antimony-hearing flue, baghouse, and CottreH dusts, drosses, and slags. These materials may be treated to recover elemental antimony or antimonial lead from which antimony oxide or sodium antimonate may be produced. 

Recycling of antimony provides a large proportion of the domestic supply of antimony. Secondary antimony is obtained from the treatment of antimony-hearing lead and tin scrap such as battery plates, type metal, beating metal, antimonial lead, etc. The scrap are charged iato blast furnaces, reverberatory furnaces, or rotary furnaces, and an impure lead bulHon or lead alloy is produced. Pure lead or antimony is then added to meet the specifications of the desired lead—antimony alloy. 

Industrial Consumption. The total consumption of primary antimony fell during the period from 1970 to 1986 (Table 3) because of the declining demand for antimony in most types of metallic uses. Since 1986, the demand for primary antimony in antimonial lead has increased, probably because of an increase in demand for starting—lighting—ignition (SLI) batteries. Total consumption in nonmetallic uses has remained stable. However, an increasing proportion of this is made up of flame retardant uses. Currendy, batteries and flame retardants are the two largest markets for antimony. 

Antimony Alloys. Approximately one-half of the total antimony demand is for metal used in antimony alloys. Antimonial lead is a term used to describe lead alloys containing antimony in proportions of up to 25%. Most commercial lead—antimony alloys have antimony contents less than 11%. The compositions of several important antimony alloys are given in Table 4. 

Demand for high performance SLI batteries has led to the development of smaller, lighter batteries that require less maintenance. The level of antimony is being decreased from the conventional 3—5% to 1.75—2.75% to minimise the detrimental effects. Lead alloys that contain no antimony have also been introduced. Hybrid batteries use a low antimony—lead alloy in the positive plate and a calcium—lead alloy in the negative plate. 

Type metal, another tin—antimony—lead alloy, is used primarily in reHef or letterpress printing. Antimony is added to increase hardness, minimize shrinkage, permit sharp definition, and reduce the melting point of the alloy. There has been a substantial decrease in the use of type metals as a result of the emergence of less expensive typesetting techniques. 

The washed slime is dried and melted to produce slag and metal. The slag is usually purified by selective reduction and smelted to produce antimonial lead. The metal is treated ia the molten state by selective oxidation for the removal of arsenic, antimony, and some of the lead. It is then transferred to a cupel furnace, where the oxidation is continued until only the silver—gold alloy (dorn) remains. The bismuth-rich cupel slags are cmshed, mixed with a small amount of sulfur, and reduced with carbon to a copper matte and impure bismuth metal the latter is transferred to the bismuth refining plant. 

In catalytic incineration, there are limitations concerning the effluent streams to be treated. Waste gases with organic compound contents higher than 20% of LET (lower explosion limit) are not suitable, as the heat content released in the oxidation process increases the catalyst bed temperature above 650 °C. This is normally the maximum permissible temperature to which a catalyst bed can be continuously exposed. The problem is solved by dilution-, this method increases the furnace volume and hence the investment and operation costs. Concentrations between 2% and 20% of LET are optimal, The catalytic incinerator is not recommended without prefiltration for waste gases containing particulate matter or liquids which cannot be vaporized. The waste gas must not contain catalyst poisons, such as phosphorus, arsenic, antimony, lead, zinc, mercury, tin, sulfur, or iron oxide.(see Table 1.3.111... 

Schwefel-. of sulfur, sulfur, sulfuric, sulfide of, thio-. siilfo-. -abdruck, m. sulfiir print, -alkali, n. alkali siilfide. -alkohol, m. siilfur alcohol, thiol carbon disulfide (old name), -ammonium, -ammon, n. ammonium sulfide, -antlmon, n. antimony sulfide, -antimonblei, n, antimony lead sulfide (Min.) boulanger-ite. 

Prengaman, R. E., Structure Control of Non-Antimonial Lead Alloys via Alloy Additions, Heat Treatment and Cold Working, Pb80, Ed. Proc. 7lh Ini. Lead Conf., Madrid, Lead Development Association, London (1983)... 

Prominent among the heavy metals found in the wastewater generated in the copper sulfate industry are copper, arsenic, cadmium, nickel, antimony, lead, chromium, and zinc (Table 22.11). They are traced to the copper and acids sources used as raw materials. These pollutants are generally removed by precipitation, clarification, gravity separation, centrifugation, and filtration. Alkaline precipitation at pH values between 7 and 10 can eradicate copper, nickel, cadmium, and zinc in the wastewater, while the quantity of arsenic can be reduced through the same process at a higher pH value. 

Semimetal that occurs as a tin-type, brittle form and as a yellow, unstable, nonmetallic form. Its main use is in alloys to harden other metals. Without the addition of antimony, lead would have remained the "softy" of the Periodic Table. But with antimony, lead ruled the print world and later found use in the production of rechargeable batteries. It can be found in older ceramic glazing (yellow orange). Everyday encounters antimony sulfide in match heads and red rubber, antimony oxide is used as a flame retardant. Pure antimony is starting to become of interest in the electronics sector. 

Antimony (Sb), 3 41-56, 56. See also Group Ill-Sb system InAsSb alloy InSb photodiode detectors/arrays Lead-antimony alloys Low antimony lead alloys Stib- entries in babbitts, 24 797 catalyst poison, 5 257t chemical reactions, 3 42—44 in coal, 6 718 economic aspects, 3 47-48 effect of micro additions on silicon particles in Al-Si alloys, 2 311-312 effect on copper resistivity, 7 676t environmental concerns, 3 50 gallium compounds with, 12 360 health and safety factors, 3 51 in pewter, 24 798... 

Low-antimony lead alloys, 14 770 Low-birefringence polycarbonates, 19 822 Low-blush copolymers, 26 538 Low boiling node, in separating nonideal liquid mixtures, 22 303 Low-calorie beer, 3 577 Low calorie sweeteners, 12 38 Low calorific value (LCV) gas, 26 575—576... 

The word bismuth is derived from the German word Weissmuth, or white substance. It is the heaviest stable element of the periodic table. Even though it carries the status of heavy metal, this metal is rated as relatively nontoxic and noncarcinogenic, unlike its neighboring elements (in the periodic table) like arsenic, antimony, lead, and tin, which are highly toxic. This nontoxicity arises from the insolubility of its salts in neutral aqueous solutions such as biological fluids, which... 

Absorbent Earth Antimony Lead Acid of Sea-salt... 

The most active catalyst is platinum applied in finely divided form, for example platinised asbestos. Certain elements, especially arsenic and mercury, have a powerful effect in reducing the activity of the platinum, a quantity of arsenic equal to 0-2 per cent, of the weight of the platinum reducing the activity by 50 per cent.5 These poisons, as they are termed, also include less harmful substances such as antimony, lead, bismuth, etc. The presence of small quantities of rhodium, iridium or osmium in the platinum also causes diminished yields of trioxide, but the presence of palladium or ruthenium has the opposite effect.6... 

Sodium, potassium, mercury and silver do not alloy with tantalum even at high temperatures 5 attempts to prepare alloys with arsenic, antimony, lead, zinc and tellurium have also failed, but the formation of an alloy with silver, copper and tin for making a dental amalgam with mercury has recently been claimed.6... 

---