SEOS

Selenaies(VI) resemble sulphates but can be reduced more easily - to SeOs " -f-115 volts). Alums are formed. Pyroselenates, [OsSeOSeOs] " are known. 

Selenium dioxide, SeO, is ery poisonous (cf. p. I47), but is valuable particu larly for the oxidation of methylene ( CHs) groups to carbonyl ( CO) groups. 

Selenium trioxide, SeO, is white, crystalline, and hygroscopic. It can be prepared by the action of sulfur trioxide on potassium selenate or of phosphorous pentoxide on selenic acid. It forms selenic acid when dissolved in water. The pure trioxide is soluble in a number of organic solvents. A solution in Hquid sulfur dioxide is a selenonating agent. It is stable in very dry atmospheres at room temperature and on heating it decomposes first to selenium pentoxide [12293-89-9] and then to selenium dioxide. 

Other inorganic selenium compounds include sodium selenocyanate [4768-87-0], NaSeCN, which is prepared by melting together selenium and sodium cyanide selenocyanogen [27151 -67-3] (SeCN)2 sodium selenosulfate [25468-09-1], Na2SeS02, which is prepared by dissolving selenium in aqueous sodium sulfite (acidification decomposes this compound) and selenate alums, eg, Al2(Se0 2 I SeO [13530-59-1]. 

The possibility of preconcentration of selenium in form of SeO by evaporation of low alkali water solution (for 20-1000 J.g/L) has been investigated. Considerable losses of selenium have been observed during evaporation of acidic and neutral solutions owing to volatility of selenium compounds. During evaporation of low alkali solutions at ph 9-10 there are no losses of selenium. Relative error of selenium determination is 1-2% for 1000 P-g/L solution and 3-5% for 20-100 p.g/L. Concentration factor is 10. 

Geon and Seo [47] also determined the effect of vulcanization time on the adhesion of natural rubber to brass-plated steel. For relatively short times, there was a peak at the end of the copper profile that corresponded well with a peak in the sulfur profile. Similarly, peaks in the zinc and oxygen profiles corresponded well. These results showed that copper sulfide and zinc oxide mostly formed at short times but some evidence for formation of zinc sulfide was also obtained. For long times, the peak in the sulfur profile no longer corresponded with that in the copper profile. Instead, the peak in the sulfur profile corresponded to the peak in the zinc profile. It was concluded that the formation of zinc sulfide increased substantially at long times. An increase in vulcanization time correlated well with a decrease in the force required to pull brass-plated steel wires out of rubber blocks. 

---