Tables For Evaluation Bateman Equation Coefficientes For Radioactivity Calculations
Tables For Evaluation Bateman Equation Coefficientes For Radioactivity Calculations
10, O C T O B E R 1 9 5 4 1595
coarse sintered-glass disk, heating the face of the disk a short of methanol, and adjust the pH to 3.0 to 3.5 with dilute mag-
time in the flame, and “sticking” the two together. The coarse nesium acetate or perchloric acid. Rapidly add about 90no
sintered-glass disk must fit the cation exchange tube closely. of the required barium chloride or perchlorat,e, then add 5 drops
The juncture between the disk and capillary tube need not be of Alizarin Red S and tit,rate to t’he first permanent pink. .411ow
tight and only strong enough to withstand the operations of in- a time lapse of 3 to 5 seconds between addition of the last few
w t i o n and removal. Gum rubber tubing ( 2 mm.) and a capil- increments of titrant.
lary tubing tip attached to the column outlet gave an adjustable For t,it.rations on a semimicro scale use a 0.2- to 0.8-millimole
head. If the head n a s maintained a t 35 cm the liquid level sample, 10 ml. of water, 10 ml. of methanol, and 1 drop of indi-
stopped automatically a t the top of the resin, thus requiring lem cator.
operator attention. Fourteen milliliters of resin in this column Ion Exchange Procedure. .\gitate the resin (H form) in a
quantitatively removed sodium from nine samples containing 1 beaker and decant the finer particles. Repeat this several times.
millimole each of sulfuric acid and sodium chloride. The re- With the column open pour in 14 ml. of resin, measured wet.
moval of metal ions is more efficient from less acid Pqlutions. Backwash with a slow stream of distilled water for a few minutes,
According to Samuelson ( 4 ) the removal of sodium ions is more then place the sintered-glass disk, with capillary tube attarhed,
difficult than all other common ions except lithium. on top of the resin column and run 50 ml. of 3 . 5 S hydrochloric
acid t,hrough from the bottom at. a flow rate of about 4 ml. per
REAGENTS .AND SOLUTIONS minute, washing it through with distilled n-ater. Continue the
washing until only a faint chloride test is obtained. This n-ill re-
Alizarin Red S. Prepare a 0.27?0 aqueous solution. quire about 150 ml. and 30 minutes.
iZmmonium Sulfate. Prepare a 0. lOOOM solution by dissolv- Introduce the 5-ml. sample containing 1 millimole of sulfate
ing 13.214 grams of ammonium sulfate in water and diluting to by pipet directly onto the resin column and !?ash through with
exactly 1liter. 20 ml. of distilled water in small portions, allon-ing the liquid level
Barium Chloride. Prepare a stock solution which is approsi- to come to rest a t t,he top of the resin column each time before
niately 0.1Jf. ..idjust t,he p H to 3 to 3.5. Standardize against a new rinse is added. Titxate the sulfate in the eluate by the
a standard solution of sulfuric acid using the procedure dexrihed standard macroprocedure.
helow.
Barium Perchlorate. Prepare a 0.1Jf stock sclution and ad-
just the pH to about, 3. Standardize against a standard solution LITERATURE CITED
of sulfuric acid using the procedure described below.
Cation Exchange Resin. Dowex 50, cross-linking 16, 50- to (1) Johnston, J., andddanis. L. H., J . A m . C h e m . Soc.. 33, 829 (1911).
100-mesh resin. (2) Kolthoff, I. M., and Stenger, V. A,, “Tolumetric Analysis,” 1-01,
Hydrochloric .4citi. Dilute reagent grade hydrochloric acid 11. pp. 30G14, New T o r k , Inter>cience Publishers, 1947.
to 3 m - . (3) I b i d . , Vol. I,p. 92.
Xagnesium .\cet,ate. approsimately 0.25M solution. (4) Samuelson, O., Snensk Kcm. T i d s k r . , 52, 115 (1940).
Methanol, .1.C.S. grade. (5) Schroeder, W. C., IND.Esc,.(:HEY., . ~ s . L L . ED..5, 403 (1933).
Sulfuric Acid. Prepare an approximately 0.01X stock solu- (6) Willard, H. H., and Furman, N. H., “Elementary Quantitative
tion and standardize by titration with a standard sodium h>-- .halysis,” 3rd ed., p. 171, Sew York, D. Van Xostrand Co.,
droside solution. 1940.
o-(2-H~droxy-~,R-tlisulfo-1-11aphthglazo)-benzenearsonicAcid
Disodium Salt (Thorin). Prepare a 0.025% solution of the so- RECEIVED for reT.iew October 12. 1‘133. .Iccepted .Jiily 14, 1954 Pi,esented
dium salt in water. before the Division of Analytical Clleuiistry a t the 123th AIeeting of the
PROCEDURE .‘ivERIcAs C H E M I C A L fiocrsTS. Kansas City. M o . Contribution f r o m the
Institute for Atomic Research a n d Department of Chemistry, Iowa State
General Procedure. For macrotitration dissolve a sample con- College, Ames, Iowa. Work Iierforined in the .IIIICS Lahoratory oi t h e
taining 2 to 4 millimoles of sulfate in 45 ml. of water, add 40 ml. Atomic Ehergy Commission.
Tables of decay constants and functions thereof are ford et al., 5 ) . The solution of the general case of n products is
presented to simplify the problem of calculating the given by
constants involved in the Bateman equation. These
tables make it possible to calculate any constant in- 2 V = S‘ (Cle-X11 + C?e-X21 . . , C,,e-hrd)
XU238
11 10 x (hPo9" - y) 9 182360493
(-57)
8.623519937
(-40)
-2.00871355S
( - 13)
-6.173709113
(-57)
1 883679420
(-562
-6.726321355
( - 53)
- 1.34857064A
(-36)
12 11 X (XPb2Io - y) 9.167742877 -2.862033615 1.974941841 -6.163333169 1.8801h3568 -6.624526361 2.827139233
(-66) (-46) (-17) -
( 66) ( -6.5) ( - 62) (-42)
13 12 X (XBi2lo- Y) 1.465110651 -3 621129523 -1,941422493 -9.849714035 3,00471689cl -1.058666459 1.411535043
(-71) (-52) ( - 19) (-72) (-71) (-67) (-48)
14 13 X (hPoZiO - I/) 8.493318974 9.950022789
(-59)
1.908771053
(-21)
-5.709919245
(-79)
1.74184l,011
(-78)
-6.135708236
(-75)
-2.878719301
(-54)
(-79
15 14 X (XPbZo6- 4.147022513 - 3 313881194 -1 876679820 5 067404016 -4.782437390 8.308920780 6.037812590
(-96) (-65) ( - 23) (-92) (-91) (-86) (-60)
XPo2'3 APbZ" AB,! ' AP0214 XTIz 0 XPb"' XBI"~ XPo?'@ APb2'fi
2.076881753
( - 15)
- 5.995996591
(5)
4.519312361
(-32)
7.038077303
(-27)
2.989975992
(-57)
-2.641439872
(-17) .
2.630448184
(6)
-8.208984851
( - 37)
-1.343918303
( - 30)
1.371642965
(-21)
1600 ANALYTICAL CHEMISTRY
4CKNOWLEDGMENT (3) Ginninrrs, D. C.. Bell. -\. F..and Tier. D. '1.. J . Research .Vat,?.
Bztr.%tandards, 50, i5-9 (1953).
This study was made by t'ie u. S. Geological SutTel- 011 h- (4) Hollander, j. hi., Perimarl, I., and Seaborg. G T., Rets. Mod.
half of the U. S. Atonlie Energy Commission. Phys., 25,469-651 (1953).
(5) Rutherford, E., Chadwicak, J., arid Ellis, E. C . , "Radiations from
Radioactive Substances.' London, Cambridge University Preas,
LITER4TURE CITED 1930. 0
(1) Baternan. H.. Cambridge Phil. SOC.Proc., 15, 423-T (1910). (6) Way, K., Fano, L., Scott, 11.It., and Thew, K..Satl. Bur. Stand-
(2) Fleming, E. H., Jr., "The Specific Alpha Activities and Half Lives ards, Circ. 499 (19.50).
of Uranium-234. Uranium-235, and Uranium-238," u. s. 1 I w w m for review January 4, 1954. .4ccep,ted .July 12. 1954. Publi-
Atomic Energy Commission, AECD 3395 (1952). cation authorized by the Director. U. S.Geological Surrey.
In an acidimetric method for the determination of the fact that zinc sulfitltx, particularly fired (crystallized) zinc
surface zinc oxide on zinc sulfide phosphors the zinc sulfide, is not attacked hy weak hydrochloric acid. Zinc sulfide
oxide is determined directly by titration with weak will not dissolve above a pH of about 2.4 ( 5 ) . Any reaction is
hydrochloric acid, under which condition the zinc still further slowed because the zinc sulfide is in a fired state. No
sulfide is not dissolved. The limit of detection of zinc hydrogen sulfide was detectable during the titration.
oxide is approximately 0.027~. The zinc oxide is determined acidimet,rically by direct titration
with 0.1-V hydrochloric acid. -1weighed sample is slurried with
water, and is titrated to the nirthj-1 orange end point. Per cent
tions concerning the effects of oxygen on luminescence, it became where n is milliliters of wid, .Y is the normality of the acid, and S
necessary to determine the amount of zinc oxide surface layer. is the weight of sample taken, in grams.
Two-step digestion methods have been reported for zinc
oxide-zinc sulfide mixtures, wherein the zinc oxide is digested, PROCEDURE
and zinc is then determined by a standard method ( 2 ) . Shakhov To 10 ml. of distilled water, add 1 drop of methyl orange
( 4 ) used a polarographic method t o determine zinc oxide in zinc indicator (0.1%) and enough acid to develop fully the pink acid
sulfide, and Rooksby ( 3 ) has reported detecting as little as 0.2% color of the indicator (about 1 drop of 0.LV hydrochloric acid).
Add the weighed sample, 0.5 to 1.0 gram, and stir to break u p
zinc oxide in zinc sulfide by x-ray diffraction methods. The the aggregates. If there is no change in the indicator color, zinc
method evolved in the present investigation takes advantage oi oxide is absent.