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Uranium and radon estimation in some water samples from Himalayas

1988, International Journal of Radiation Applications and Instrumentation. Part D. Nuclear Tracks and Radiation Measurements

The uranium content of water samples collected from Kumaun (Uttar Pradesh) and Stwaltk (Htmachal Pradesh) Himalayas has been estimated using the technique of fission track registration in lexan plastic. The uranium content has been found vary from 1.08 + 0.02 to 35.83 + 0.09 ppb. The radon estimation has also ~een made in the-same water samples using LR-115, type II plastic track detector. The radon content has been found to vary from 2.68 + 0.23 to 12.55 + 0.93 pCt/1. No direct correlation has ~een found betwee~ uranium and radon contents. However, the high values of uranium in the mineralized areas confirm that the fission track method can successfully be employed for uranium exploration.

Nucl. Tracks Radiat. Meas., Vol. 15, Nos. 1-4, pp. 791-793, 1988 Int. J. Radiat. Appl. lnstrum., PartD 0191-278X/89$3.00 + .00 (~) 1989Pergamon Press plc Printed in Great Britain URANIUM A N D R A D O N E S T I M A T I O N IN SOME WATER SAMPLES F R O M H I M A L A Y A S R.C. RAMOLA, SURINDER SINGH and H.S. VIRK Department of Physics, Guru A~ritlsr-143005, Nanak Dev University, India. A b s t r a c t - The u r a n i u m c o n t e n t o f w a t e r samples c o l l e c t e d from Kumaun ( U t t a r P r a d e s h ) and S t w a l t k ( H t m a c h a l P r a d e s h ) Himalayas has been e s t i m a t e d u s i n g t h e t e c h n i q u e o f f i s s i o n track registration in lexan plastic. The u r a n i u m c o n t e n t has been found v a r y f r o m 1 . 0 8 + 0 . 0 2 t o 3 5 . 8 3 + 0 . 0 9 ppb. The radon e s t i m a t i o n has a l s o ~een made i n the-same w a t e r samples u s i n g LR-115, t y p e I I p l a s t i c t r a c k d e t e c t o r . The radon c o n t e n t has been f o u n d t o v a r y from 2 . 6 8 + 0 . 2 3 t o 12.55 + 0.93 p C t / 1 . No d i r e c t c o r r e l a t i o n has ~een found betwee~ uranium and radon c o n t e n t s . However, t h e h i g h values of uranium in the mineralized areas confirm that the fission track method • can successfully be employed for uranium exploration. 1. INTRODUCTION Uranium can be measured by v a r i o u s t e c h n i q u e s v t z . a c t i v a t i o n enalTats, mass s p e c t r o m e t r y , f l o u r e s c e n c e and d e l a y e d n e u t r o n c o u n t i n g . Since the d i s c o v e r y o f s o l i d s t a t e n u c l e a r t r a c k d e t e c t o r s , an a d d i t i o n a l method i s a v a i l a b l e t o d e t e r m i n e t h e u r a n i u m c ° n c e n t r a t t ° n l i D o r o c k s and m i n e r a l s o f both the terrestrial and extra-terrestlal origin " . The track etch t e c h n i q u e w h i c h i s f i n d i n g many t e c h n o l o g i c a l applications6,7, can be e a s i l y used t o f t n d u r a n i u m c o n t e n t i n w a t e r . The r a d o n d e t e c t i o n i n w a t e r indicates the high potential f o r d e t e c t i o n of s t r u c t u r a l f e a t u r e s as w e l l as u r a n i u m o c c u r r e n c e 8. Rag e t a l . 9 c a r r i e d o u t t h e r a d o n measurements i n the hot springs for investigation of geothermal energy sources. In present s t u d y , a s i m p l e a p p a r a t u s e m p l o y i n g LR-115, t y p e I I p l a s t i c as a l p h a t r a c k r e c o r d e r i s used t o d e t e c t t h e a l p h a a c t i v i t y o f w a t e r samples c o l l e c t e d f r o m Kumaun ( U t t a r P r a d e s h ) and S t w a l t k (Htmachal P r a d e s h ) Himalayas due t o radon. Uranium e s t i m a t i o n i s made i n w a t e r u s i n g f i s s i o n track technique to study its correlation with radon. 2. EXPERIMENTS The e x p e r i m e n t a l p r o c e d u r e f o r u r a n i u m e s t i m a t i o n reported elsewherelO-13. The u r a n i u m c o n c e n t r a t i o n using the formula: TM i n w a t e r i s same as in water is determined (I) Cw = VGNA E~ o w h e r e symboles have t h e i r u s u a l m e a n i n g s . The method p r o v i d e s a d e t e c t i o n limit o f 0 . 0 1 ppb and a p r e c i s i o n i s s t a t e d t o be + 1 0 - 1 5 ~ and +5 ~ ( R e f . 1 4 and 1 5 ) . The a p p a r a t u s used t o d e t e c t a l p h a a c t i v i t y due t o r a d o n i s same as reported elsewherel3. 200 ml of each sample i s t a k e n i n r a d o n t i g h t r e a g e n t b o t t l e o f one l t t r e capacity connected with a conical flask through a hand o p e r a t e d r u b b e r pump and t h e g l a s s b u l b c o n t a i n i n g CaCI2 t o a b s o r b moisture. LR-115, t y p e I I p l a s t i c t r a c k d e t e c t o r s each 1 cm2 i n area a r e suspended i n t h e c o n i c a l f l a s k f o r a p e r i o d o f 15 d a y s . The radon gas i s t r a n s f e r e d from t h e r e a g e n t b o t t l e t o t h e c o n i c a l f l a s k by b u b b l i n g w a t e r and s u c k i n g t h e gas w i t h t h e h e l p o f a hand o p e r a t e d r u b b e r pump. A l l t h e d e t e c t o r s a r e e t c h e d i n 2.5N NaOH s o l u t i o n a t 60oc f o r 2 h r s and a r e scanned u n d e r an o p t i c a l m i c r o s c o p e f o r t r a c k d e n s i t y m e a s u r e m e n t s . Track density is converted into radon activity i n p C t / 1 by u s t u g a c a l i b r a t i o n c o n s t a n t (1 p C i / 1 o f r a d o n c o r r e s p o n d s t o 16.8 t r a c k s / c m 2 f o r 15 days 791 792 R . C . R A M O L A et al. exposure p e r i o d ) determined by Stngh e t a l . 16 i n t h i s l a b o r a t o r y . Detect i o n l i m i t of radon d e t e r m i n a t i o n was found to be 0.5 p C i / 1 by t h i s t r a c k etch method, w i t h a p r e c i s i o n of 5 - 1 0 ~ . The d e t e c t i o n l i m i t can f u r t h e r be lowered by increasing the exposure p e r i o d . 3. RESULTS AND DISCUSSION The r e s u l t s f o r uranium and radon c o n t e n t i n water samples are given i n Table 1. The uranium c o n t e n t i n the w a t e r samples i s determined by using Table 1. Radon and Uranium c o n c e n t r a t i o n Sample location UTTAR PR~DESH Nanak Mats A1Dh~ T r a c k A n a l y s t s Track d e n s i t y Radon a c t i v i t y (tracks/cmi) (pCi/1) Kancht Mandir R a t i Ghat Kharana Panyali Kalarmal Guralt 83 146 45 143 211 45 50 158 144 45 HIMACHAL PRADESH Samur Kalan Rameda 166 181 Bhimtal Nainital Llnglot 4.94~0.36 8.69~0.48 2.68_+0.23 i n water samples F.T. A n a l y s i s T o t a l No. U c o n t e n t of t r a c k s (ppb) 5.46_+0.04 1.66~0.02 1.82+0.02 12.55~0.93 2,68+0.23 2.98+0.25 9.40~0.59 8.57_+0.55 2,68¢0.24 11616 3520 3872 2304 4928 5856 9312 6432 4992 20560 9.8820.89 10.77+0.86 38688 76164 18.20+_0.07 35,83_+0.09 8.51_+0.79 1.08+0,02 2.32_+0.02 2.75+0.03 4.38+0.03 3.03+0.03 2.35_+0.02 9,68+0.07 equation 1. The uranium values i n Samurkalan and Rameda areas of H.P. and G u r a l t area of U.P. are found c o m p a r a t i v e l y h i g h e r than i n other areas. Atomic Minerals D i v i s i o n , Department of Atomic Energy, I n d i a has a l r e a d y r e p o r t e d the presence of uranium i n Samur Kalan and Rameda areas. The presence of uranium i n w a t e r samples can be due to the f o l l o w i n g two possibilities: ( l ) U r a n t u m p r e s e n t i n suspended or c o l l o i d a l i m p u r i t i e s . (2) Uranium d e r i v e d by the l e a c h i n g of rocks through which the water traverses. The suspended i m p u r i t i e s , i f p r e s e n t i n large s i z e , are easy to f i l t e r , b u t when the s i z e i s v e r y s m a l l , they w i l l give r i s e to c l u s t e r of t r a c k s whereas they are deposited i n t h i n f i l m . The number of c l u s t e r s found i n our study was n e g l i g i b l e and i f any, the number of t r a c k s i n a c l u s t e r d i d not exceed 100. I t r u l e s out the c o n t r i b u t i o n of uranium due to suspended impurities. The radon values i n water samples are found to vary from 2.68_+0.23 to 12.55+0.93 p C i / 1 . The water samples from Kanchi Mandir, BhimtaI, L i n g l o t , PanyaTi and Kalarmal areas have y i e l d e d e x c e p t i o n a l l y high values of radon c o n t e n t i r r e s p e c t i v e of t h e i r low U c o n t e n t v a l u e s . The high values of radon i n these areas may be due t o radium separated from u r a n $ ~ and precipitating f o r a long time on the w a l l s of f r a c t u r e d rocks A . No d i r e c t c o r r e l a t i o n was found between radon a c t i v i t y and uranium c o n t e n t . However, both the radon and uranium values are found h i g h e r i n Samur Kalan and Rameda areas, which may be due t o the presence of uranium i n these areas. 4 . CONCLUSIONS The h i g h v a l u e s o f u r a n i u m i n m i n e r a l i z e d a r e a s c o n f i r m t h a t t h e f i s s i o n t r a c k method c o u l d be s u c c e s s f u l l y employed in the uranium exploration. Radon e s t i m a t i o n method c a n be u s e d a s an a d d i t i o n a l t e c h n i q u e . However, t h i s technique may g i v e some spurious anomalies due t o the presence of URANIUM AND R A D O N ESTIMATION 793 radium. 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