Selenium deposition

Moksnes, K. 1983. Selenium deposition in tissues and eggs of laying hens given surplus of selenium as selenomethionine. Acta Vet. Scand. 24 34-44. 

Hiraka S, Hahashi M. The influence of selenium deposits on silver plating on adhesive strength. In Proc. 29th An. Int. Reliability Physics Symp. Apr. 1991 8-11. 

Hiraka, S., and Habashi, M., The Influence of Selenium Deposits on Silver Plating on Adhesive Strength, Proc. 29 An. Inti. Reliability Physics Symp., pp. 8-11 (Apr. 1991)... 

These data were derived from values for the influence of cadmium on selenium deposition in tissues, assuming a 1 1... 

This chapter is an attempt to present the important results of studies of the synthesis, reactivity, and physicochemical properties of this series of compounds. The subject was surveyed by Bulka (3) in 1963 and by Klayman and Gunther (4) in 1973. Unlike the oxazoles and thiazoles. there are few convenient preparative routes to the selenazoles. Furthermore, the selenium intermediates are difficult to synthesize and are often extremely toxic selenoamides tend to decompose rapidly depositing metallic selenium. This inconvenience can be alleviated by choice of suitable reaction conditions. Finally, the use of selenium compounds in preparative reactions is often complicated by the fragility of the cycle and the deposition of metallic selenium. 

Deposits. Selenium forms natural compounds with 16 other elements. It is a main constituent of 39 mineral species and a minor component of 37 others, chiefly sulfides. The minerals are finely disseminated and do not form a selenium ore. Because there are no deposits that can be worked for selenium recovery alone, there are no mine reserves. Nevertheless, the 1995 world reserves, chiefly in nonferrous metals sulfide deposits, are ca 70,000 metric tons and total resources are ca 130,000 t (24). The principal resources of the world are in the base metal sulfide deposits that are mined primarily for copper, zinc, nickel, and silver, and to a lesser extent, lead and mercury, where selenium recovery is secondary. 

Tellurium and many other impurities remain undissolved. The solution is filtered and cooled to reverse the reaction and to deposit soHd selenium. Oeselenized liquor is recycled to the dissolution step. 

N. D. Sindeeva, Mineralogy andTypes of Deposits of Selenium and Tellurium, Interscience Pubhshers, a division of John Wiley Sons, Inc., New York, 1964. 

Like selenium, tellurium minerals, although widely disseminated, do not form ore bodies. Hence, there are no deposits that can be mined for tellurium alone, and there are no formally stated reserves. Large resources however, are present in the base-metal sulfide deposits mined for copper, nickel, gold, silver, and lead, where the recovery of tellurium, like that of selenium, is incidental. 

Dilution with water reverses the reaction, and heating the solution Hberates sulfur dioxide. Upon being added to a solution of teUurides, teUurium forms colored polyteUurides. Unlike selenium, teUurium is not soluble in aqueous sodium sulfite. This difference offers a method of separating the two elements. Like selenium, teUurium is soluble in hot alkaline solutions except for ammonium hydroxide solutions. Cooling reverses the reaction. Because teUurium forms solutions of anions, Te , and cations, Te" ", teUurium films can be deposited on inert electrodes of either sign. 

Production and Economic Aspects. Thallium is obtained commercially as a by-product in the roasting of zinc, copper, and lead ores. The thallium is collected in the flue dust in the form of oxide or sulfate with other by-product metals, eg, cadmium, indium, germanium, selenium, and tellurium. The thallium content of the flue dust is low and further enrichment steps are required. If the thallium compounds present are soluble, ie, as oxides or sulfates, direct leaching with water or dilute acid separates them from the other insoluble metals. Otherwise, the thallium compound is solubilized with oxidizing roasts, by sulfatization, or by treatment with alkaU. The thallium precipitates from these solutions as thaUium(I) chloride [7791 -12-0]. Electrolysis of the thaUium(I) sulfate [7446-18-6] solution affords thallium metal in high purity (5,6). The sulfate solution must be acidified with sulfuric acid to avoid cathodic separation of zinc and anodic deposition of thaUium(III) oxide [1314-32-5]. The metal deposited on the cathode is removed, kneaded into lumps, and dried. It is then compressed into blocks, melted under hydrogen, and cast into sticks. 

Amorphous (vitreous) selenium, vacuum-deposited on an aluminum substrate such as a dmm or a plate, was the first photoconductor commercially used in xerography (6). It is highly photosensitive, but only to blue light (2). Its light absorption falls off rather rapidly above 550 nm. Because of the lack of photoresponse in the red or near infrared regions, selenium photoreceptors caimot be used in laser printers having He—Ne lasers (632.8 nm), or soHd-state lasers (680—830 nm). 

Selenium 0.05 0.05 Hair or fingernail loss numbness in fingers or toes circulatory problems Discharge from petroleum refineries erosion of natural deposits discharge from mines... 

Selenium was isolated some 35 y after tellurium and, since the new element resembled tellurium, it was named from the Greek askrivr], selene, the moon. The discovery was made in 1817 by the Swedish chemist J. J. Berzelius (discoverer of Si, Ce and Th) and J. G. Gahn (discoverer of Mn) they observed a reddish-brown deposit during the burning of sulfur obtained from Fahlun copper pyrites, and showed it to be volatile and readily reducible to the new element. 

The dyestuffs in which a 4-aIkyl group was present were obtained amorphous—in spite of variation of the reaction conditions, they could not be brought to crystallization. No deposition of selenium which might have resulted from a ring fission could be observed. 

Applications Although a wide range of metals can be sputtered, the method is often commercially restricted by the low rate of deposition. Applications include the coating of insulating surfaces, e.g. of crystal vibrators, to render them electrically conducting, and the manufacture of some selenium rectifiers. The micro-electronics industry now makes considerable use of sputtering in the production of thin-film resistors and capacitors . ... 

The solution should be free from the following, which either interfere or lead to an unsatisfactory deposit silver, mercury, bismuth, selenium, tellurium, arsenic, antimony, tin, molybdenum, gold and the platinum metals, thiocyanate, chloride, oxidising agents such as oxides of nitrogen, or excessive amounts of iron(III), nitrate or nitric acid. Chloride ion is avoided because Cu( I) is stabilised as a chloro-complex and remains in solution to be re-oxidised at the anode unless hydrazinium chloride is added as depolariser. 

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