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Renseignements : POUR PLUS DE RENSEIGNEMENTS SUR VEUILLEZ VOUS ADRESSER À : la reproduction du contenu Services de publication du MDNM l'achat des publications du MDNM Vente de publications du MDNM les droits d'auteurs de la Couronne Imprimeur de la Reine PAR TÉLÉPHONE : Local : (705) 670-5691 Numéro sans frais : 1 888 415-9845, poste 5691 (au Canada et aux États-Unis) Local : (705) 670-5691 Numéro sans frais : 1 888 415-9845, poste 5691 (au Canada et aux États-Unis) Local : 416 326-2678 Numéro sans frais : 1 800 668-9938 (au Canada et aux États-Unis) PAR COURRIEL : [email protected] [email protected] [email protected] cjOMNR-OGS 1981 Ministry of Natural ^te^lan w- Pope W.T Foster Deputy Minister Ontario ONTARIO GEOLOGICAL SURVEY Open File Report 5368 Grant #38 Radon Decay Products - U Exploration by Keith Bell and J.W. Card 1981 Parts of this publication may be quoted if credit is given. It is recommended that reference to this report be made in the following form: Bell, Keith, and Card, J.W. 1981: Radon Decay Products - U Exploration, Ontario Geological Survey OFR 5368, 16 p. Ontario Geological Survey OPEN FILE REPORT Open file reports are made available to the public subject to the following conditions: This report is unedited. Discrepancies may occur for which the Ontario Geological Survey does not assume liability. Recommendations and statements of opinion expressed are those of the author or authors and are not to be construed as statements of government policy. Open file copies may be read at the following locations: Mines Library Ontario Ministy of Natural Resources 8th Floor, 77 Grenville Street, Toronto The office of the Regional or Resident Geologist in whose district the area covered by this report is located. Handwritten notes and sketches may be made from this report. Check with the Library or Region al or Resident Geologist's office as to whether there is a copy of this report that may be borrowed. The Library or Regional or Resident Geologist's office will also give you information on copying ar rangements. A copy of this report is available for Inter-Library Loan. This report is on file in the Regional or Resident Geologists' office(s) located at: All Regional and Resident Geologists The right to reproduce this report is reserved by the Ontario Ministry of Natural Resources. Permission for other reproductions must be obtained in writing from the Director, Ontario Geological Survey. E.G. Pye, Director Ontario Geological Survey ONTARIO GEOSCIENCE RESEARCH GRANT PROGRAM Final Research Reports, 1981 Preface This publication includes one final report on a research project that terminated March 31, 1981 and was funded under the Ontario Geoscience Research Grant Program. A requirement of the Program is that recipients of grants are to submit final reports within six months after termination of funding. Many of the research projects supported in 1978-79 (the first year of the Grant Program) were planned for three years. As a result, an unusually large number (19) of final reports were received this year. Unlike previous years, each report has been put on a separate Open File. A final report is defined as a comprehensive summary stating the findings obtained during the tenure of the grant, together with supporting data. It may consist, in part, of reprints or preprints of publications and copies of addresses given at scientific meetings. It is not the intent of the Ontario Geological Survey to formally publish the final reports for wide distribution but rather to encourage the recipients of grants to seek publication in appropriate scientific journals whenever possible. The Survey, however, also has an obligation to ensure that the results of the research are made available to the public at an early date. Although final reports are the property of the applicants and the sponsoring agencies, they may also be placed on an open file. This report is intended to meet this obligation. E.G. Pye Director Ontario Geological Survey December 1981 11 GRANT 38 RADON DECAY PRODUCTS - U EXPLORATION Keith Bell and J.W. Card Geology Department, Carleton University, Ottawa. ABSTRACT The spontaneous deposition of short-lived radon decay products onto solid surfaces ("collectors") provides the basis for a simple and efficient way of prospecting for uranium. The alpha-activity of two of the decay products, 218p o an(3 214p Of can fce measured by conventional counting techniques following the exposure of a collector to a radon source. Laboratory studies have shown: (i) radon decay products can be collected on a wide variety of materials, (ii) the number of radon decay products increases with the surface area of the collectors, (iii) the number of decay products collected is greater when the collectors are negatively charged, (iv) the shape of the collectors is relatively unimportant, and (v) reproducibility is about 5% of the measured values. Field tests, carried out on known uranium anomalies, involved the suspension of collectors into holes in the soil. After an overnight exposure, the collectors were removed and their alpha-activity counted. The data readily delineated radon anomalies at three different sites. In addition, some of the anomalies were outlined using activity measurements from collectors suspended above soil aliquots in sealed containers. The activity of the radon decay products deposited onto collectors provides an effective method for delineating radon anomalies in uranium exploration. The field techniques are simple to apply, and results are available after short exposure times (about 18 hours) and after short counting intervals (5 minutes). 1. INTRODUCTION Radon, because of its inert and gaseous nature, has already been used extensively as a geochemical tracer for buried uranium deposits. Among the methods available are soil-gas sampling (Dyck, 1969a; 1969b; Bowie et al., 1971; Morse, 1976), alpha-particle track counting (Gingrich, 1975; Gingrich and Fisher, 1976; Beck and Gingrich, 1976), solid-state alpha-particle detection (Gaucher, 1976; Warren, 1977), and the collection of radon on activated charcoal. 222 Rn (ti s 3.824 days), a member of the 238 U decay series, is produced by the decay of 22 ^Ra (ti s 1599 years), and in turn yields a series of four short-lived decay products, 218 Po (t! ^ 3.05 minutes, 214 Pb (ti = 26.8 minutes), 214 Bi (ti = 19.7 minutes), and 214 Po (ti - 1.64 x 10~4 seconds). Of these, 2 l 8 Po and 2 ^ 4 Po can be detected using alpha particle counting techniques. It has only recently been realized that the collection of these short-lived decay products may be useful in uranium exploration. Our earlier results have been published elsewhere (Card and Bell, 1979). Here our most recent findings are summarized. LABORATORY STUDIES The collection of radon decay products was initially studied under controlled laboratory conditions. Each test involved the exposure of a "collector" (any solid surface that collects radon decay products) to a radon-bearing 2. atmosphere, followed by the counting of the alpha activity from the collected decay products, 218p o an ^ 214p Of Each collector was inserted into a ZnS(Ag)-coated scintillation chamber and counted for a 5 minute interval. Our earlier work had shown that radon itself does not become attached to the collectors and that approximately steady-state activity is reached after an exposure of about 3 hours. Key problems that remained involved the determination of the optimum material and shape for the collectors, and an evaluation of the effect of surface area on collecting efficiency. The most significant findings are summarized below: (1) Metal, plastic, and cardboard plates of similar size and shape resulted in similar activities. (2) Collectors exposed in 226 mL containers with 10 g aliquots of CANMET Standard BL-3 (a crushed ore bearing 1.02^^ U) yielded excellent reproducibility with a standard deviation of iS'fc. (3) The amount of activity was substantially greater on those collectors with greater surface areas. (4) Collectors in the form of discs and open-ended hollow cylinders showed no advantages over simple rectangular plates. (5) Activity on the collectors showed an almost linear relationship with sample mass, although for a given soil aliquot the activity is greater for a smaller container. 3. (6) The activity on the collectors corresponds to the theoretical growth curve for 222^n . equilibrium conditions are approached after 15 days. (7) The radon decay products seem to be firmly attached to the collectors; attempts to remove them by rinsing in water were unsuccessful. (8) Activity on copper plates was significantly increased by negatively charging the collectors during the last few hours of the exposure. a factor of about 2.7. Sensitivity was enhanced by Surface area of the collector is less important for the charged plates; very small plates provided almost as much activity as the larger ones. Although the activity reached a plateau at about -60 V, sensitivity was greatly increased by applying a potential as low as -10 V. Tests with positively charged plates showed that only a small number of decay products were collected. On the basis of these laboratory observations a series of field tests were undertaken to evaluate the collector method for uranium exploration. FIELD TESTS Initial field tests were carried out at a radon anomaly associated with a small uranium occurrence in Palaeozoic sedimentary rocks at South March, 20 km west of Ottawa, Ontario (see Card and Bell, 1979). Collectors suspended in covered holes (20 cm in diameter and roughly 35 cm deep) 4. collected a sufficient number of decay products to readily delineate the anomaly. Related tests, involving the suspension of collectors above soil aliquots in sealed containers, showed also that there was sufficient radium in the soil to allow a successful delineation of the anomaly. In-situ measurements were obtained from soil-covered areas overlying uranium-bearing pegmatites in Grenville Province rocks; the pegmatites take the form of concordant, tabular bodies in gneisses and marbles. At one of the test sites, in Palmerston Township, Ontario (Lat. 44 0 54' 15" N, Long. 76 0 44' 45" W), the suspension of collectors in inverted flower pots resulted in a higher activity than recorded using the covered holes. Readings taken at regular intervals across the strike of the regional structural trend are shown in Figure l(b), along with a cross-section of the geology (Figure l(a)). anomalous zones. The radon profile indicates three The most significant occurs immediately to the west of the main pegmatite, and probably reflects either the extension of the pegmatite under the overburden, or radium-bearing detritus from the pegmatitic source. Four stations yielded anomalous values; one, at over 1300 cpm, represents the highest number of counts yet documented by the collector method. Analyses of the soils from the Palmerston occurrence also clearly delineated the main anomaly (Figure l(c)). At another test site, in Blithfield Township, Ontario (Lat. 45 0 16' 25" N, Long. 76 0 48' 20" W), a pegmatite in 5. high grade Grenville gneisses and marbles is exposed in cross section at a road cut. Although only about l m wide the pegmatite produced a radon anomaly that was readily detected. Assessment of the overall reproducibility of the activity measurements under in-situ conditions involved monitoring a single hole at the Palmerston site eight times during a 30 day period. The reproducibility was of the order of ±15* of the mean number of the counts. At South March three holes were monitored every hour for a period of six hours and the reproducibility was better than 2(^. Data from one of these holes yielded a reproducibility of 5%. These measurements are in surprisingly good agreement with one another, in spite of the fact that many workers (i.e., Kraner et al., 1964) have reported large secular variations in radon concentrations in soil gas. THE THORON PROBLEM In thorium-enriched terrains decay products from 22 ^Rn (radon produced from the 232-pn d ecay series, normally referred to as thoron) may be collected and counted along with the 2 38u-produced radon decay products. Such results could well produce anomalously high readings that bear no relationship to the distribution of 238|j series nuclides. Although the half-life of thoron is only 55.6 seconds, the half-lives of two of the thoron decay products, 2 ^ 2 Pb (ti 10.64 hours) and 212 Bi (ti - 60.60 minutes), are much longer 6. than those of the ^n d ec ay products and this feature can be used to apply a correction to the collector readings. Tests using 2 g of Th(C03)2 show that the thoron decay products, like those of radon, can be collected but their subsequent behaviour differs in the following ways: (1) The decay curve for an assemblage of collected thoron decay products is quite different from that for the radon decay products. The thoron decay products decay much more slowly than those of radon. (2) Exposures longer than 48 hours are required before equilibrium is reached between thoron and its decay products. In contrast an exposure of only 3 hours produces a steady-state radon decay product activity. (3) Removal of the collector after a short exposure (up to a few hours) results in an increase in activity for the first few hours. This is probably due to the collection of 212pjDf a beta emitter. The subsequent decay of 212pb to 212gi an ^ 212p Of both alpha emitters, increases the amount of activity observed on the collectors. The observed thoron decay product curves are consistent with the shapes expected from the equations for successive transformations. Thoron decay product activity can thus be simply checked by counting the collector a second time, about 5 to 6 hours after the initial reading. During this time the activity of the radon (222^n ) decay products decays to 7. negligible levels. The decay rate of the thoron decay products is, however, dominated by the longer half-lives of 212pb an(3 212gi^ an(3 the count rate after 5 hours changes only slightly. Counting a second time thus yields data which can be used to estimate the thoron contribution to the initial measurements. Thoron corrections applied at the Palmerston Township test site showed that only negligible amounts of thoron decay products were present on the collectors. The extent to which thoron migrates is limited by its short half-life (55.6 seconds) and it may well be that only relatively small amounts were able to migrate to the collector. COMPARATIVE STUDIES We have also used the South March site for evaluating different uranium exploration techniques, and these results will form the basis of a future paper. Included are data for in-situ radon surveys using alphameters (Gratton, 1980) and the soil-gas suction method (Christie, 1980). Analyses of soils for radium, both by total digestion, (Wilson, 1979) and immersion methods, (Bradley, 1979), and uranium by fluorimetry and delayed neutron analysis were also obtained. The results from the collector method for in-situ measurements and soil sample analyses compared favourably with the results obtained from these conventional techniques. 8. CONCLUSIONS The field and laboratory results reported here provide some interesting insights into the application of the collector method to radon measurement. The successful testing at three different sites shows that the collectors can be used to locate radon anomalies in a variety of geological environments. A commercially-available instrument package (the Alphacard system) based on the collector method has recently been designed by Alpha Nuclear Company of Mississauga, Ontario. The simplicity of the collector method and its ease of use are factors that are much in its favour as a uranium exploration tool. ACKNOWLEDGEMENTS The geology of the Palmerston area was kindly shown by K.L. Ford of the Geological Survey of Canada, and A.J.M. Limited allowed access to the property. REFERENCES Beck, L.S. and Gingrich, J.E. 1976: Track-Etch Orientation Survey in the Cluff Lake Area, Northern Saskatchewan; Canadian Inst. Min. and Met. Bull., 69, No. 769, p 104-109. Bowie, S.H.U., Ball, T.K. and Ostle, D. 1971: Geochemical Methods in the Detection of Hidden Uranium Deposits; p. 103-111 in Canadian Inst. Min. and Met., Spec. Vol. 11. Bradley, C.J. 1979: Delineation of a Soil Radium Anomaly; An Evaluation of a Soil-Immersion Technique; unpubl. B. Se. Thesis, Carleton University, Ottawa, Ontario, 43 p. Card, J.W., and Bell, K. 1979: Radon Decay Products and their Application to Uranium Exploration; Canadian Inst. Min. and Met. Bull., 72, No. 812, p 81-87. Christie, D.S. 1980: Radon-Thoron Survey of a Known Uranium-Copper Occurrence: An Evaluation of a Soil-Gas-Suction Emanometry Technique; unpubl. B.Se. Thesis, Carleton University, Ottawa, Ontario, 37 p. Dyck, W. 1969a: Field and Laboratory Methods Used by The Geological Survey of Canada in Geological Surveys, No. 10; Radon Determination Apparatus for Geochemical Prospecting for Uranium; Geol. Surv. Canada, Pap. No. 68-21, 30 p. 1969b: Development of Uranium Exploration Methods Using Radon; Geol. Surv. Canada, Pap. No. 69-46, 25 p. Gaucher, E. 1976: Alphameters: Uranium Prospecting by Radon Detection; Canadian Min. J., 97, April, 1976, p. 28-34. Gingrich, J.E. 1975; Results from a new Uranium Exploration Method; Soc. of Min. Eng. of AIME, Trans., 258, p 61-64. Gingrich, J.E. and Fisher, J.C. 1976: Uranium Exploration Using the Track-Etch Method; p. 213-227 in Exploration for Uranium Ore Deposits, I.A.E.A. Proc. Gratton, F.J. 1980: Radon Variations in Soil Gas at the South March Uranium-Copper Occurrence; unpubl. B.Se. Thesis, Carleton University, Ottawa, Ontario, 45 p. lo. Kraner, H.W., Schroeder, G.L., and Evans, R.D. 1964: Measurements of the Effects of Atmospheric Variables on Radon-222 Flux and Soil-Gas Concentrations; p. 191-215 in The Natural Radiation Environment, University of Chicago Press. Morse, R.H. 1976: Radon Counters in Uranium Exploration; p. 229-239 in Exploration for Uranium Ore Deposits, I.A.E.A. Proc. Warren, R.K. 1977: Recent Advances in Uranium Exploration with Electronic Alpha Cups; Geophysics, 42, p. 982-989. Wilson, J.S. 1979: Soil-Radium Geochemistry of a Uranium-Copper Occurrence, South March, Ontario; unpubl. B.Se. Thesis, Carleton University, Ottawa, Ontario, 26 p. UJ 'o o CN •o - o "c o O "S O —— l/) c 3 ULJ O O c o 0) J o o. 0) u CO E -C a ok. D) S JD *-fc- a k. a M! o o ok. a k. o u c o x 0 u U O 0) O) 0) JD o *- "O c o E o k. D) O C c o o u o Q. X o O) JO Q. J^ "o o -C u o u •n -f •o l o T o o •o o o CM o o 00 o o (ajnujuj jed S4unoD) o o CN CO o o CM o U (94nujai jsd (D "O UO kD O)
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