V O L U M E 21, NO. 6, J U N E 1 9 4 9 Table 1.
Effect of Treatment with Perchloric and Hydrofluoric Acids 1-0
Loss
Aodiom, potassium
Copper. silver, gold Beryllium, magnesium Calcium strontium barium z i n c , oahrnium, meicury Lanthanum, cerium Titaniurn, thorium Tin, lead Vanadium Risiiiuth .\lolybdenuin, tungsten, uranium I r o n , cobalt, nickel
Apparent Lo.. Boron. 100%
Selenium, varies greatly Manganese, up t o 3% Rhenium, varies greatly
for aluminum was gravimetric, and the appareiit loss was due to the inability of fuming perchloric acid t o remove all fluoride associated with the aluminum as a complex ion. This complex prevents the precipitation of hydrous aluminum oxide in the usual manner (3). XOattempt is made to explain the loss of niaiigaiiese; but Hoffman and Lundell (4)observed that mang:inese conipounds ivere slightly volntile from mixed perchloric and hydrochloric acid solutions. Tlie eight other elements which shon-ed loes on treatment with the acid mixture were expected to do so. Boron and silicon fluorides are very volatile (8). Selenium forms at least two volatile fluorides (14). iintimony and arsenic form volatile fluorides ( l l ) ,as do chromium ( I O ) , germanium ( I ) , and rhenium (12). According to Ruff (II), molybdenum and tungsten form volatile fluoi,ides and oxyfluorides. T o such fluorides are formed, however, when salts of these elements are fumed with the acid mixture, despite the vigorous dehydrating action of concentrated perchloric acid. I n contrast chromium is easily volatilized as the osyfluoride from the acid mixture. This indicates that it is virtuslly impossible t o predict the volatility of many elements from mixed acid solutions. Selenium and rhenium are appreciably volatile from fuming perchloric acid solutions alone, as might be expected from the physical properties of the oxides of these acid-forming elements (9, 15). The volatilit,y of rhenium, under these conditions, has been suggested (6).
701 The results of this investigation show that nine clcments, if present in a material that is subjected to routine analyticnl treatment ri-ith perchloric and hydrofluoric acids, will t i c lost in varying amounts. Consequently, determination of any of thebe elements in the resulting solution would give low v:ilucs bnsed on the original material. -\CKSOI’LEDGhlENT
Tlie authors are iridehted to the CLinadian (’rili!)c’i’ Il(jfirir.rs Limited of >fontreal for generosity in supplying high-purity elementary selenium, to The Eagle-Pic1ir.r Compn~iyRcsearch Laboratories for generosity in supplying high-purit y gcmiariiuni dioxide, and to A , D. Jfelaven, University of Triincwv, for promptly supplying high-purity potwsium rhcn:itc (\-I1 ). LITERATURE CITED
Fischer, W., and Weidemann, W., 2.anorg. allgt,rri. L’hern., 213, 106-14 (1933). Hillebrand, W.F., and Lundell, G. E. F., “Apj)licd Inoi.g:tiiic .4nalysis,” New York, John Wiley R: Sons. 1929. Ibid., p. 390, line 5 ; p. 730, footnote 89. Hoffman, J. I., and Lundell, G . E. F., J . Research .Vutl. B u r . Standards, 22, 465-70 (1939). Lundell, G . E. F., and Hoffman, J. I., “Outlines of LMetliodj of Chemical Analysis,” pp. 24-9, New York, John Wiley & Sons, 1929. Ibid., pp. 46-7. Marvin, G . G.. and Woolaver, L. B., I s n . ENG.CHEM.,ASAL. ED.,17, 474 (1945). Noyes, A. A , and Bray, W. C . , “System of Qualitative Analysis for the Rare Elements,” pp. 35-7, New York, Jlacmillan Co., 1927. Ogawa, E., Bull. Chem. SOC.J a p a n , 7, 265-73 (19323. Oliveri, diV., Gazz. chim. ital., 16, 218 (1886). Ruff, O., 2 . angcw. Chem., 20,1217 (1907). Ruff, O., and Kwasnik, W., Ibid., 47, 480 (1934). Smith, G. F., “Perchloric Acid,” pamphlet, 4th ed., p. 15, Columbus, Ohio, G. Frederick Smith Chemical Co., 1940. Yost, D. M., and Russell, H. J., “Systematic Inorganic Chemistry,” p. 299, New York, Prentice-Hall, 1944. Ibid., p. 318. Zernicke, J., Chem. Weekblad, 36, 748-50 (1939). RECEIVED August 7, 1948.
Determination of Alumina in Steel A Spectrochemical Method R. H. COLIS k Y D D. A. GARDNER Carnegie-Illinois Steel Corporation, G a r y Steel Works, Gary, I n d .
T
H E extensive use of aluminum in the steel-making industry as a deoxidizer, for control of grain size, etc., has created H need for an accurate ant1 rapid means of determining aluminum iii steel. The aluminum may be present in steel in solid solution and as compounds such as alumina, *112Os, and aluminum nitride, Al2N2. Aluminum present in solid solution is soluble in hydrochloric acid. The aluminum compounds are insoluble. Khen alumina is determined in steel, the insoluble rpsidue is Fashed with a solution of sodium carbonate to ensure the renioval of any nitrides left undissolved by washing with dilute acid (1). In this paper the term “alumina” designates the combined aluminum that remains in the residue after the sodium rnrhonate wash. Gravimetric and volumetric methods of analysis for alunlina, because of the many separations and reprecipitations involved, have proved t,oo tedious and time-consuming when a relLttively
large number of samples are to be analyzed. Coloriiiictric arid photometric procedures also are too involved, because they require the complete removal of iron and other int,erfering elements before comparison can be made. S o particular problems were encountered in the spectrographic determination of the total aluminum which is carried out in this laboratory by means of pressed pellets made from drillings or millings of the steel using a high voltage condensed spark for excitation. Total aluminum results obtained in this manner are, for practical purposes, independent of the concentration of alumina. Results on several samples analyzed spectrogr~bphically for total aluminum containing alumina in concentrations as high as 0.06% were in good agreement with the chemical results obtained on the same samples. Because spectrographic analysis does not provide a direct meaiis for distinguishing between acid-insoluble and acid-
ANALYTICAL CHEMISTRY
202
A chemical separation of the acid-soluble and acid-insoluble c o m p o n e n t s of the steel is made. The a l u m i n u m present in the acid-insoluble portion, a f t e r removal of aluminum nitride, is oonsidered as being the a l u m i n u m oxide in the steel. The acid-insoluble portion is fused a n d t a k e n u p in a weal
