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Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
105
Indoor Radon Concentration Measurement in Selected Factories in
Northern and Central Iraq
Ammar A. Battawy1*
, Mohamad Suhaimi Jaafar1
, Nada F. Tawfiq2
, Iskandar Shahrim Mustafa1
, Ammir Hassan Ali3
and Zakariya Adel Hussein1
1. School of Physics, USM, Malaysia.
2. Department of Physics, College of Science, AL-Nahrain University, Iraq.
3. Department of Physics, College of Education, Mosul University, Iraq.
*
E-Mail: ammar_physics@yahoo.com
Abstract
In this work, the outdoor radon concentration level and lung cancer risks have been measured in selected locations in
northern and central Iraq during the summer season 2012 by using time integrated passive radon dosimeters
containing LR-115 Type II plastic track detectors. These measurements were carried out in the factories for an
exposure time of 60 day. The radon concentration in these factories ranges from (36.36 – 125.10) Bq.m-3
with an
average of (59.93Bq.m-3
), which within the acceptable radon levels (50-150) Bq.m-3
recommended by the
International Commission on Radiological Protection (ICRP). The average absorption effective dose equivalent for a
person living in factories for which the investigation were done was found to be (1.425mSv.y-1
). It is observed that
the average lung cancer per year per 106
person was found to be 25.654.
Keyword: LR-115 Type II nuclear track detectors; Radon concentration; AEDE; PAEC.
1. Introduction
The radon isotopes are produced from the decay of the natural radio nuclides (235
U), (232
Th) and (238
Rn) mainly
because of their short half-life are not as important as (222
Rn). (222
Rn) can be considered to be of the most dangerous
radioactive elements in the environment. Its character as a noble gas allows it to spread through the atmosphere [1].
The main natural sources of indoor are soil, building materials (sand, rocks, cement, etc), water born transport,
natural energy sources like (gas, coal, etc) which contains traces of( 238
U) [1, 2]. The indoor radon consecration
depends mainly on radon exhalation from surrounding materials. (222
Rn) and is airborne daughters can cause a
significant internal health hazard (for example lung cancer) especially when uranium or radium content in the soil is
high or when the radon and its daughters are concentrated in enclosed area and in particular in dwelling. Several
reports have appeared in literature demonstrating that residential radon may be responsible for 7% of lung cancer in
Germany, 4% in Netherlands, 20% in Sweden and (10-15%) in the united states [3].
Concentration of (222
Rn) gas in dwelling gas been reviewed and summarized by the UNSCEAR, data available for
over 20 European countries and these show that average radon concentration varies widely, from (<25 Bq.m-3
in) the
Netherlands, the united kingdom and Cyprus, to over 100 Bq.m-3
in Estonia, Finland, Sweden, Luxembourg, the
Czech republic, Hungary and Albania for many countries, the variation in indoor radon levels within the country is
enormous, and individual dwellings with radon gas concentrations above (10000 Bq.m-3
) have been found in
Finland, Norway, Sweden, Belgium, Germany, Switzerland, the united kingdom, the Czech republic and Spain
[4, 5].
Measurement of indoor radon is rather important because the radiation dose to human constitutes more than 60% of
the total dose, including that from the natural sources [6]. Several techniques have been used to measure radon and
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
106
is daughters concentration. Solid state unclear track detectors, such as LR-115 and CR-39, have been widely used
for the measurement of time integrated radon levels in dwellings under different conditions [7-12].
The present study aims to measure some important parameters such as the outdoor radon (222
Rn) concentration in
selected factories, the potential alpha energy concentration, the absorption effective dose exposure and the lung
cancer cases per year per 106
person. These evaluations can help in stabling a reference level of activity
concentrations from which any further increase in those levels for any reason could be detected.
2. Experimental procedure
This study assesses the indoor radon concentration in selected factories in northern and central Iraq. LR-115 Type II
nuclear track detector sheets of active layer 12 µm thick were used. These sheets were cut into small pieces of
1.5×1.5cm2
area each. The sheets were stored under normal laboratory conditions, and then suspended in ceilings for
two months in places under study (exposed in Bare mode). The track density so obtained was converted into the
units of Bq m-3
of radon concentration using the calibration factor determined by Subba Ramu et al. (1988) and
assuming an equilibrium factor of 0.4 between radon progeny and radon [13], the detectors were collected and
chemically etched using solution of 2.5 N of NaOH at temperature of (60 o
C) for 2 hours. After etching, the
detectors were rinsed in distilled water and cleaned. An optical microscope with a magnification of 400X was used
to count the number of tracks per cm2
in each detector.
Figure 1 shows the calibrations curve for radon standard samples and track density. Radon concentration in the
samples was measured by comparing between track density registered on the detectors and that of the standard
derived from equation 1 [14]. LR-115 detectors were positioned in direct contact with the outdoor air at several
specific locations in Iraq for 60 days as shown in (Figure 2). During exposure, alpha particles emitted by radon,
thoron and their progenies bombarded the detectors.
Cx = x. (Cs/s) (1)
Where and are the induced fission track densities for unknown sample and standard solution (in tracks/mm2
)
respectively, while Cx and Cs denote the uranium concentration for unknown sample and standard solution (in µg/l)
[15].
The following parameters were deduced from technique:
1- The Potential Alpha Energy Concentration (PAEC) in Working Level (WL) of radon daughters is estimated
using the following equation [1, 16].
Cd=F CRn/3700 (2).
Where F is the equilibrium factor and equal to 0.4 and CRn is the activity concentration of radon in Bq.m-3
.
2- The Absorption Effective Dose Equivalent (AEDE) is estimated by using the dose conversion factor
5.5 mSv/WLM [1, 17].
AEDE (mSv.y-1
) = (5.5mSv/WLM) × (WLM/y) (3)
3- The lung cancer per year/106
person is estimated by using the risk factor lung cancer induction 18×10-6
mSv-1
[1, 17].
Lung cancer per year par 106
person = AEDE (mSv.y-1
) × 18×10-6
(mSv-1
) (4)
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
107
3. Results and discussions
The results of the radon concentration in air samples of factories were given in Table (1) and it was observed that
they varied from 36.36 Bq/m3
in North Fertilizer Plant factory to 125.10 Bq/m3
in Phosphate factory, the result
shows that the average radon concentration in samples from the phosphate factories (highest) is a factor of 2.59
higher than that from the ceramic factory (lowest), similarly the average radon concentration in samples from the
MST (Ministry of Science and Technology) is a factor of 2.24 higher than the average radon concentration in
samples from the ceramic factory, and the average radon concentrations in samples from the glasses, ceramic,
detergent chemicals, North Oil, Mishraq Sulphur , and North Fertilizer Plant factories are similar to each other.
This illustrates that the phosphate factories and MST had radon levels higher than other factories in this study, but it
is acceptable because it lies within the radon levels recommended by the international commission on radiological
protection (ICRP), and the average radon concentration for all factories (except phosphate) also within the
acceptable radon levels (50 - 150) Bq/m3
recommended by the international commission on radiological protection
(ICRP) [18].
Table (2) is summarized the value of radon concentration CRn (Bq/m3
), the potential alpha energy concentration
PAEC (WL), the absorption effective dose exposure AEDE (mSv.y-1
) and the lung cancer per year per 106
person.
The values of radon concentration for all locations ranged from (36.31 to 125.10) Bq/m3
with the average value of
59.93 Bq/m3
, the highest value of potential alpha concentration (PAEC) levels in the phosphate factory 13.5 mWL
with average value of 12.2 mWL, likewise MST had an average value of potential alpha concentration (PAEC)
levels of more than 10 mWL. While most of the factories had average value of potential alpha concentration (PAEC)
levels less than 5 mWL, the lowest value 3.9 mWL and average value of 6.5 mWL was evident for all locations. The
absorption effective dose exposure equivalent ranged from (0.864 to 2.975) mSv.y-1
with an average value of
1.43 mSv.y-1
. The report (ICRP) recommended that action levels of radon should be within a range of (3-10 mSvy-1
)
[19, 12]. According to this study, the radon induced lung cancer risk ranged from (15.56 to 53.56) per million
persons, with an average of about 25.65 per million persons, the phosphate factory and MST had similar value of the
radon induced lung cancer risk per year at more than 40 per million persons, but all the other factories had  20 per
million persons.
4. Comparison with some other results
Table 3 shows a comparison of average values of the radon concentration in Bq/m3
for some countries. The results
in this study were in agreement with data available in another study for Jordan and less than other findings in
Pakistan, India, Spain and north Iraq but greater than findings in Hong Kong, Italy, Japan Canada and south Iraq.
5. Conclusion
The higher radon concentrations in air samples were 125.10 Bq/m3
from Phosphate factorie, and the minimum
concentrations 36.36 Bq/m3
from North Fertilizer Plant, the average radon concentration in samples from phosphate
factories (highest) and MST is a factor of (2.59 and 2.24) higher than from ceramic factory (lowest). These average
radon concentrations in samples from all factories except Phosphate factory are close to each other.
The radon induced lung cancer risk was measured ranges from (15.56 to 53.56) per million persons, with an average
of about 25.65 per million persons. Therefore the Phosphate factory is the most dangerous than all factories at this
study.
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
108
References:
1. H. H. Mansur, S. per Khdar, H.Y. Abdulla, N.Q. Muhamad, M.M. Othman and S. Qader, (2005). Measurement
of indoor radon levels in Erbil capital by using solid state nuclear track detector, Radiation Measurement, 40,
544-547.
2. A. Banman, D. J. Hervat, N. Lokobauer and K. J. In Vahra, (1982), Natural Radiation Environment. Willy
Rastern Ltd, New Delhi, p.401.
3. J.H. Lubin, (2003), Studies of radon and lung cancer in North America and China, Radiation Protection
Dosimetry, 104, (4), 315- 319.
4. UNSCEAR "United Nations Scientific Committee on the Effect of Atomic Radiation. Sources and Effects of
Ionizing Radiation", (2000).Vol.1: Sources (New York: United Nations).
5. S. C. Darby and D. C. Hill, (2003), Health effects of residential radon: A European perspective at the end of
2002, Radiation Protection Dosimetry, 104, (4), 321-329.
6. UNSCEAR "United Nations Scientific Committee on the Effect of Atomic Radiation", (1998), United Nations
New York.
7. R. Barillon, D. Klein, A. Chambaudet, F. Membrey and M. Fromm, (1991), Additional uses of polymeric
nuclear track detectors (CR-39 and LR-115) for measuring radon emanation, Nuclear Tracks. Radiat.Meas.,
19, (1-4), 291-295.
8. K. M. Abumurad, M. K. Kullab, B. A. Al-Bataina, A. M. Ismail and A. D. Lehlooh, (1994), Estimation of
radon concentrations inside houses in some Jordanian regions, Mu'tah Journal for Research and Studies, 9, (5),
9-21.
9. M. S.Garawi, M. R. Baig and M. D. Al-anazy, (2004), Indoor radon distribution inside different rooms of
residential buildings in Riyadh, Saudi Arabia, Sci. Int. (lahore), 6, (1), 81- 82.
10. P. Tuccimei, M. Moroni and D. Norcia, (2006), Simultaneous determination of 222
Rn and 220
Rn exhalation rates
from building materials used in Central Italy with accumulation chambers and a continuous solid state alpha
detector: Influence of particle size , humidity and precursors concentration, Applied Radiation and Isotopes,
64, 254- 263.
11. R. M. Yousuf, M. M. Husain and L. A Najam, (2009), Measurement of 222
Rn concentration levels in Spring
Water in Iraq, Jordan Journal of Physics, 2, (2), 89-93.
12. Ammar A. Battawy and Hana I. Hussein, (2010), Study of Radon Concentration and Lung Cancer Risk in The
Right Area of Shirkatt District, J. of University of Anbar for pure science, 4, (1).
13. S. Singh, R. Malhotra, J. Kumar and L. Singh. (2001). Indoor radon measurements in dwellings of Kulu area,
Himachal Pradesh, using solid state nuclear track detectors, Radiation Measurements, 34, 505–508.
14. Zeena J. R. Abd Ali. (2009). Study The Effect of High Voltage Power Lines on Radon Concentrations in Air
Using Solid State Nuclear Track Detector CR-39, MSc. Thesis, College of Education, Baghdad University,
Iraq.
15. Ahmed F. Saleh Al –Jobouri, (2012). Determination of Uranium Concentration in Human Urine for Selected
Regions in Iraq Using Laser-Induced Kinetic Phosphorimetry and CR-39 Nuclear Track Detector, MSc Thesis,
College of Science, Al-Nahrain University, Iraq.
16. J.H. Lubin and 13 others, (1996), Lung cancer in radon-exposed miners and estimation of risk from indoor
exposure, J.Nati .cancer Inst, 87, 817-827.
17. C. Reto and B. Werner, (1989), The radon problem, Radiat. Phys., 34, (2), 251-259.
18. ICRP "Protection against 222
Rn at home and work", (1993), Publication 65, Ann of ICRP 25-3.
19. K. Skeppström and B. Olofsson, (2007), Uranium and radon in groundwater, European Water, 17/18, 51-62.
20. H. R. M. Al-Gaim, I. J. M. Al-Khalifa and M. A. A. Al-Helal, (2012), Indoor Radon Measurements in the
Dwellings and Multistory Buildings of Basrah Technical Institute (Iraq), Journal of Basrah Researches
((Sciences)), 38, (1.A), 8 – 13.
21. M. M. Al-Kofahi, B. R. Khader, A. D. Lehlooh, M. K. Kullab, K. M. Abumurad and B. A. Al-Bataina, (1992),
Measurement Of Radon 222 In Jordanian Dwellings, Nucl. Tracks Radiat. Meas. 20, (2). 371-382.
22. K. Abumurad, B. Al-Bataina, A. Ismail, M. Kullab and A. Al-Eloosy, (1997), A survey of radon levels in
Jordanian Dwellings during an autumn season, Radiation protection dosimetry, 69, (3), 221 – 226.
23. K. N. Yu, T. Cheung, Z.J. Guan, B.W.N. Mui and Y.T. Ng, (2000), 222
Rn, 220
Rn and their progeny
concentrations in offices in Hong Kong, Journal of Environmental Radioactivity, 48, 211-221,.
24. M. H. Magalhães, E.C.S. Amaral, I. Sachett and E.R.R. Rochedo, (2003), Radon-222 in Brazil: an outline of
indoor and outdoor measurements, Journal of Environmental Radioactivity, 67, 131–143.
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
109
25. L. Sesana, E. Caprioli and G.M. Marcazzan, (2003). Long period study of outdoor radon concentration in
Milan and correlation between its temporal variations and dispersion properties of atmosphere, Journal of
Environmental Radioactivity, 65, 147–160.
26. S. Oikawa, N. Kanno, T. Sanada, N. Ohashi, M. Uesugi, K. Sato, J. Abukawa and H. Higuchi, (2003). A
nationwide survey of outdoor radon concentration in Japan, Journal of Environmental Radioactivity, 65, 203–
213.
27. R. Kumar, A. K. Mahur, H. Singh, R. G. Sonkawade and R. Swarup, (2010), Radon levels in some dwellings
around the international monument Taj Mahal, Agra using SSNTDs, Indian journal of pure & applied physics,
48, 802 – 804.
28. K. Badhan, R. Mehra and R.G. Sonkawade, (2011). Studying the Variation of Indoor Radon Levels in
Different Dwellings in Hoshiarpur District of Punjab, India, Indoor Built Environ, 000, 1–6.
29. R. C. Ramola, (2011). Survey of radon and thoron in homes of indian himalaya, Radiation Protection
Dosimetry, 146, (1–3), 11–13.
30. S. Kansal, R. Mehra, N.P.Singh, (2012), Life time fatality risk assessment due to variation of indoor radon
concentration in dwellings in western Haryana, India, Applied Radiation and Isotopes, 70, 1110–1112.
31. A. M. Sánchez, J. d. T. Pérez, A.B. R. Sánchez and F.L. N. Correa, (2012). Radon in workplaces in
Extremadura (Spain), Journal of Environmental Radioactivity, 107, 86-91.
Table 1: Average, maximum and minimum radon concentration in samples (Bq/m3
)
Locations
No. of
Samples
Average radon
concentration
Maximum radon
concentration
Minimum radon
concentration
Phosphate factory 10 112.69 125.10 97.13
Glasses factory 10 44.67 46.59 42.25
Ceramic factory 10 43.51 46.39 39.93
Detergent Chemicals 4 45.04 49.48 37.52
North Oil 6 47.97 50.44 43.31
Mishraq Sulphur 6 43.68 49.19 38.48
North Fertilizer Plant 10 44.27 50.35 36.36
MST 5 97.53 103.49 91.53
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
110
Table 2: summarized the measurement of radon concentration, the potential alpha energy concentration, the
absorption effective dose exposure and the lung cancer cases per year per 106
person.
Sample Code CRn (Bq/m3
) PAEC (mWL)
AEDE (mSv.y-
1
)
Lung Cancer/106
person
Phosphate factory 112.69 12.2 2.68 48.244
Glasses factory 44.67 4.8 1.062 19.124
Ceramic factory 43.51 4.7 1.035 18.627
Detergent Chemicals 45.04 4.9 1.071 19.282
North Oil 47.97 5.2 1.141 20.536
Mishraq Sulphur 43.68 4.7 1.039 18.700
North Fertilizer Plant 44.27 4.8 1.053 18.952
MST 97.53 10.5 2.320 41.753
Table 3: A comparison of radon concentration in air in Bq/m3
for some countries
Country CRn (Bq/m3
)
PAEC
(mWL)
AEDE
(mSv/y)
Ref.
Iraq
103.98 17.2 2.47 Battawy and Hussein
13.53 - 51.176 -- -- Al-Gaim et al.
Jordan
33.28 -- -- AL-Kofahi et al.
29.3 to 99.7 -- -- Abumurad et al.
Hong Kong 48±32 5.2±5.1 -- Yu et al.
Brazil 5 - 200 -- -- Magalhaes et al.
Italy 5 - 15 -- 0.12 Magalhaes et al.
Japan 6.1 -- 0.45 Oikawa et al.
India
Taj Mahal 213 -- 1.3 - 4.4 Kumar et al.
Punjab 84.93 - 128.53 -- 1.45 - 2.19 Badhan et al.
Garhwal and Kumaun 11 - 191 -- -- Ramola
western Haryana 76 - 115.46 -- -- Kansal et al.
Spain above 400 -- -- Sánchez, et al.
Canada 41.9 -- -- Chen et al.
Iraq 59.93 6.5 1.43 Present study
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
111
Figure 1: The relation of radon concentration and track density in standard samples.
Figure 2: Arrangement of the LR-115 detector of (1.5×1.5) cm2
placed in the outdoor air. The distance between the
detectors and the ground level is 2.5 m.
Journal of Environment and Earth Science www.iiste.org
ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online)
Vol. 3, No.3, 2013
112
Figure 3: shows the histogram of radon concentration in factories
0
20
40
60
80
100
120
Phosphate
factory
Glasses
factory
Ceramic
factory
Detergent
Chemicals
North Oil Mishraq
Sulphur
North
Fertilizer
Plant
MST
CRn(Bq/m3)
Factories

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Indoor radon

  • 1. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 105 Indoor Radon Concentration Measurement in Selected Factories in Northern and Central Iraq Ammar A. Battawy1* , Mohamad Suhaimi Jaafar1 , Nada F. Tawfiq2 , Iskandar Shahrim Mustafa1 , Ammir Hassan Ali3 and Zakariya Adel Hussein1 1. School of Physics, USM, Malaysia. 2. Department of Physics, College of Science, AL-Nahrain University, Iraq. 3. Department of Physics, College of Education, Mosul University, Iraq. * E-Mail: ammar_physics@yahoo.com Abstract In this work, the outdoor radon concentration level and lung cancer risks have been measured in selected locations in northern and central Iraq during the summer season 2012 by using time integrated passive radon dosimeters containing LR-115 Type II plastic track detectors. These measurements were carried out in the factories for an exposure time of 60 day. The radon concentration in these factories ranges from (36.36 – 125.10) Bq.m-3 with an average of (59.93Bq.m-3 ), which within the acceptable radon levels (50-150) Bq.m-3 recommended by the International Commission on Radiological Protection (ICRP). The average absorption effective dose equivalent for a person living in factories for which the investigation were done was found to be (1.425mSv.y-1 ). It is observed that the average lung cancer per year per 106 person was found to be 25.654. Keyword: LR-115 Type II nuclear track detectors; Radon concentration; AEDE; PAEC. 1. Introduction The radon isotopes are produced from the decay of the natural radio nuclides (235 U), (232 Th) and (238 Rn) mainly because of their short half-life are not as important as (222 Rn). (222 Rn) can be considered to be of the most dangerous radioactive elements in the environment. Its character as a noble gas allows it to spread through the atmosphere [1]. The main natural sources of indoor are soil, building materials (sand, rocks, cement, etc), water born transport, natural energy sources like (gas, coal, etc) which contains traces of( 238 U) [1, 2]. The indoor radon consecration depends mainly on radon exhalation from surrounding materials. (222 Rn) and is airborne daughters can cause a significant internal health hazard (for example lung cancer) especially when uranium or radium content in the soil is high or when the radon and its daughters are concentrated in enclosed area and in particular in dwelling. Several reports have appeared in literature demonstrating that residential radon may be responsible for 7% of lung cancer in Germany, 4% in Netherlands, 20% in Sweden and (10-15%) in the united states [3]. Concentration of (222 Rn) gas in dwelling gas been reviewed and summarized by the UNSCEAR, data available for over 20 European countries and these show that average radon concentration varies widely, from (<25 Bq.m-3 in) the Netherlands, the united kingdom and Cyprus, to over 100 Bq.m-3 in Estonia, Finland, Sweden, Luxembourg, the Czech republic, Hungary and Albania for many countries, the variation in indoor radon levels within the country is enormous, and individual dwellings with radon gas concentrations above (10000 Bq.m-3 ) have been found in Finland, Norway, Sweden, Belgium, Germany, Switzerland, the united kingdom, the Czech republic and Spain [4, 5]. Measurement of indoor radon is rather important because the radiation dose to human constitutes more than 60% of the total dose, including that from the natural sources [6]. Several techniques have been used to measure radon and
  • 2. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 106 is daughters concentration. Solid state unclear track detectors, such as LR-115 and CR-39, have been widely used for the measurement of time integrated radon levels in dwellings under different conditions [7-12]. The present study aims to measure some important parameters such as the outdoor radon (222 Rn) concentration in selected factories, the potential alpha energy concentration, the absorption effective dose exposure and the lung cancer cases per year per 106 person. These evaluations can help in stabling a reference level of activity concentrations from which any further increase in those levels for any reason could be detected. 2. Experimental procedure This study assesses the indoor radon concentration in selected factories in northern and central Iraq. LR-115 Type II nuclear track detector sheets of active layer 12 µm thick were used. These sheets were cut into small pieces of 1.5×1.5cm2 area each. The sheets were stored under normal laboratory conditions, and then suspended in ceilings for two months in places under study (exposed in Bare mode). The track density so obtained was converted into the units of Bq m-3 of radon concentration using the calibration factor determined by Subba Ramu et al. (1988) and assuming an equilibrium factor of 0.4 between radon progeny and radon [13], the detectors were collected and chemically etched using solution of 2.5 N of NaOH at temperature of (60 o C) for 2 hours. After etching, the detectors were rinsed in distilled water and cleaned. An optical microscope with a magnification of 400X was used to count the number of tracks per cm2 in each detector. Figure 1 shows the calibrations curve for radon standard samples and track density. Radon concentration in the samples was measured by comparing between track density registered on the detectors and that of the standard derived from equation 1 [14]. LR-115 detectors were positioned in direct contact with the outdoor air at several specific locations in Iraq for 60 days as shown in (Figure 2). During exposure, alpha particles emitted by radon, thoron and their progenies bombarded the detectors. Cx = x. (Cs/s) (1) Where and are the induced fission track densities for unknown sample and standard solution (in tracks/mm2 ) respectively, while Cx and Cs denote the uranium concentration for unknown sample and standard solution (in µg/l) [15]. The following parameters were deduced from technique: 1- The Potential Alpha Energy Concentration (PAEC) in Working Level (WL) of radon daughters is estimated using the following equation [1, 16]. Cd=F CRn/3700 (2). Where F is the equilibrium factor and equal to 0.4 and CRn is the activity concentration of radon in Bq.m-3 . 2- The Absorption Effective Dose Equivalent (AEDE) is estimated by using the dose conversion factor 5.5 mSv/WLM [1, 17]. AEDE (mSv.y-1 ) = (5.5mSv/WLM) × (WLM/y) (3) 3- The lung cancer per year/106 person is estimated by using the risk factor lung cancer induction 18×10-6 mSv-1 [1, 17]. Lung cancer per year par 106 person = AEDE (mSv.y-1 ) × 18×10-6 (mSv-1 ) (4)
  • 3. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 107 3. Results and discussions The results of the radon concentration in air samples of factories were given in Table (1) and it was observed that they varied from 36.36 Bq/m3 in North Fertilizer Plant factory to 125.10 Bq/m3 in Phosphate factory, the result shows that the average radon concentration in samples from the phosphate factories (highest) is a factor of 2.59 higher than that from the ceramic factory (lowest), similarly the average radon concentration in samples from the MST (Ministry of Science and Technology) is a factor of 2.24 higher than the average radon concentration in samples from the ceramic factory, and the average radon concentrations in samples from the glasses, ceramic, detergent chemicals, North Oil, Mishraq Sulphur , and North Fertilizer Plant factories are similar to each other. This illustrates that the phosphate factories and MST had radon levels higher than other factories in this study, but it is acceptable because it lies within the radon levels recommended by the international commission on radiological protection (ICRP), and the average radon concentration for all factories (except phosphate) also within the acceptable radon levels (50 - 150) Bq/m3 recommended by the international commission on radiological protection (ICRP) [18]. Table (2) is summarized the value of radon concentration CRn (Bq/m3 ), the potential alpha energy concentration PAEC (WL), the absorption effective dose exposure AEDE (mSv.y-1 ) and the lung cancer per year per 106 person. The values of radon concentration for all locations ranged from (36.31 to 125.10) Bq/m3 with the average value of 59.93 Bq/m3 , the highest value of potential alpha concentration (PAEC) levels in the phosphate factory 13.5 mWL with average value of 12.2 mWL, likewise MST had an average value of potential alpha concentration (PAEC) levels of more than 10 mWL. While most of the factories had average value of potential alpha concentration (PAEC) levels less than 5 mWL, the lowest value 3.9 mWL and average value of 6.5 mWL was evident for all locations. The absorption effective dose exposure equivalent ranged from (0.864 to 2.975) mSv.y-1 with an average value of 1.43 mSv.y-1 . The report (ICRP) recommended that action levels of radon should be within a range of (3-10 mSvy-1 ) [19, 12]. According to this study, the radon induced lung cancer risk ranged from (15.56 to 53.56) per million persons, with an average of about 25.65 per million persons, the phosphate factory and MST had similar value of the radon induced lung cancer risk per year at more than 40 per million persons, but all the other factories had  20 per million persons. 4. Comparison with some other results Table 3 shows a comparison of average values of the radon concentration in Bq/m3 for some countries. The results in this study were in agreement with data available in another study for Jordan and less than other findings in Pakistan, India, Spain and north Iraq but greater than findings in Hong Kong, Italy, Japan Canada and south Iraq. 5. Conclusion The higher radon concentrations in air samples were 125.10 Bq/m3 from Phosphate factorie, and the minimum concentrations 36.36 Bq/m3 from North Fertilizer Plant, the average radon concentration in samples from phosphate factories (highest) and MST is a factor of (2.59 and 2.24) higher than from ceramic factory (lowest). These average radon concentrations in samples from all factories except Phosphate factory are close to each other. The radon induced lung cancer risk was measured ranges from (15.56 to 53.56) per million persons, with an average of about 25.65 per million persons. Therefore the Phosphate factory is the most dangerous than all factories at this study.
  • 4. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 108 References: 1. H. H. Mansur, S. per Khdar, H.Y. Abdulla, N.Q. Muhamad, M.M. Othman and S. Qader, (2005). Measurement of indoor radon levels in Erbil capital by using solid state nuclear track detector, Radiation Measurement, 40, 544-547. 2. A. Banman, D. J. Hervat, N. Lokobauer and K. J. In Vahra, (1982), Natural Radiation Environment. Willy Rastern Ltd, New Delhi, p.401. 3. J.H. Lubin, (2003), Studies of radon and lung cancer in North America and China, Radiation Protection Dosimetry, 104, (4), 315- 319. 4. UNSCEAR "United Nations Scientific Committee on the Effect of Atomic Radiation. Sources and Effects of Ionizing Radiation", (2000).Vol.1: Sources (New York: United Nations). 5. S. C. Darby and D. C. Hill, (2003), Health effects of residential radon: A European perspective at the end of 2002, Radiation Protection Dosimetry, 104, (4), 321-329. 6. UNSCEAR "United Nations Scientific Committee on the Effect of Atomic Radiation", (1998), United Nations New York. 7. R. Barillon, D. Klein, A. Chambaudet, F. Membrey and M. Fromm, (1991), Additional uses of polymeric nuclear track detectors (CR-39 and LR-115) for measuring radon emanation, Nuclear Tracks. Radiat.Meas., 19, (1-4), 291-295. 8. K. M. Abumurad, M. K. Kullab, B. A. Al-Bataina, A. M. Ismail and A. D. Lehlooh, (1994), Estimation of radon concentrations inside houses in some Jordanian regions, Mu'tah Journal for Research and Studies, 9, (5), 9-21. 9. M. S.Garawi, M. R. Baig and M. D. Al-anazy, (2004), Indoor radon distribution inside different rooms of residential buildings in Riyadh, Saudi Arabia, Sci. Int. (lahore), 6, (1), 81- 82. 10. P. Tuccimei, M. Moroni and D. Norcia, (2006), Simultaneous determination of 222 Rn and 220 Rn exhalation rates from building materials used in Central Italy with accumulation chambers and a continuous solid state alpha detector: Influence of particle size , humidity and precursors concentration, Applied Radiation and Isotopes, 64, 254- 263. 11. R. M. Yousuf, M. M. Husain and L. A Najam, (2009), Measurement of 222 Rn concentration levels in Spring Water in Iraq, Jordan Journal of Physics, 2, (2), 89-93. 12. Ammar A. Battawy and Hana I. Hussein, (2010), Study of Radon Concentration and Lung Cancer Risk in The Right Area of Shirkatt District, J. of University of Anbar for pure science, 4, (1). 13. S. Singh, R. Malhotra, J. Kumar and L. Singh. (2001). Indoor radon measurements in dwellings of Kulu area, Himachal Pradesh, using solid state nuclear track detectors, Radiation Measurements, 34, 505–508. 14. Zeena J. R. Abd Ali. (2009). Study The Effect of High Voltage Power Lines on Radon Concentrations in Air Using Solid State Nuclear Track Detector CR-39, MSc. Thesis, College of Education, Baghdad University, Iraq. 15. Ahmed F. Saleh Al –Jobouri, (2012). Determination of Uranium Concentration in Human Urine for Selected Regions in Iraq Using Laser-Induced Kinetic Phosphorimetry and CR-39 Nuclear Track Detector, MSc Thesis, College of Science, Al-Nahrain University, Iraq. 16. J.H. Lubin and 13 others, (1996), Lung cancer in radon-exposed miners and estimation of risk from indoor exposure, J.Nati .cancer Inst, 87, 817-827. 17. C. Reto and B. Werner, (1989), The radon problem, Radiat. Phys., 34, (2), 251-259. 18. ICRP "Protection against 222 Rn at home and work", (1993), Publication 65, Ann of ICRP 25-3. 19. K. Skeppström and B. Olofsson, (2007), Uranium and radon in groundwater, European Water, 17/18, 51-62. 20. H. R. M. Al-Gaim, I. J. M. Al-Khalifa and M. A. A. Al-Helal, (2012), Indoor Radon Measurements in the Dwellings and Multistory Buildings of Basrah Technical Institute (Iraq), Journal of Basrah Researches ((Sciences)), 38, (1.A), 8 – 13. 21. M. M. Al-Kofahi, B. R. Khader, A. D. Lehlooh, M. K. Kullab, K. M. Abumurad and B. A. Al-Bataina, (1992), Measurement Of Radon 222 In Jordanian Dwellings, Nucl. Tracks Radiat. Meas. 20, (2). 371-382. 22. K. Abumurad, B. Al-Bataina, A. Ismail, M. Kullab and A. Al-Eloosy, (1997), A survey of radon levels in Jordanian Dwellings during an autumn season, Radiation protection dosimetry, 69, (3), 221 – 226. 23. K. N. Yu, T. Cheung, Z.J. Guan, B.W.N. Mui and Y.T. Ng, (2000), 222 Rn, 220 Rn and their progeny concentrations in offices in Hong Kong, Journal of Environmental Radioactivity, 48, 211-221,. 24. M. H. Magalhães, E.C.S. Amaral, I. Sachett and E.R.R. Rochedo, (2003), Radon-222 in Brazil: an outline of indoor and outdoor measurements, Journal of Environmental Radioactivity, 67, 131–143.
  • 5. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 109 25. L. Sesana, E. Caprioli and G.M. Marcazzan, (2003). Long period study of outdoor radon concentration in Milan and correlation between its temporal variations and dispersion properties of atmosphere, Journal of Environmental Radioactivity, 65, 147–160. 26. S. Oikawa, N. Kanno, T. Sanada, N. Ohashi, M. Uesugi, K. Sato, J. Abukawa and H. Higuchi, (2003). A nationwide survey of outdoor radon concentration in Japan, Journal of Environmental Radioactivity, 65, 203– 213. 27. R. Kumar, A. K. Mahur, H. Singh, R. G. Sonkawade and R. Swarup, (2010), Radon levels in some dwellings around the international monument Taj Mahal, Agra using SSNTDs, Indian journal of pure & applied physics, 48, 802 – 804. 28. K. Badhan, R. Mehra and R.G. Sonkawade, (2011). Studying the Variation of Indoor Radon Levels in Different Dwellings in Hoshiarpur District of Punjab, India, Indoor Built Environ, 000, 1–6. 29. R. C. Ramola, (2011). Survey of radon and thoron in homes of indian himalaya, Radiation Protection Dosimetry, 146, (1–3), 11–13. 30. S. Kansal, R. Mehra, N.P.Singh, (2012), Life time fatality risk assessment due to variation of indoor radon concentration in dwellings in western Haryana, India, Applied Radiation and Isotopes, 70, 1110–1112. 31. A. M. Sánchez, J. d. T. Pérez, A.B. R. Sánchez and F.L. N. Correa, (2012). Radon in workplaces in Extremadura (Spain), Journal of Environmental Radioactivity, 107, 86-91. Table 1: Average, maximum and minimum radon concentration in samples (Bq/m3 ) Locations No. of Samples Average radon concentration Maximum radon concentration Minimum radon concentration Phosphate factory 10 112.69 125.10 97.13 Glasses factory 10 44.67 46.59 42.25 Ceramic factory 10 43.51 46.39 39.93 Detergent Chemicals 4 45.04 49.48 37.52 North Oil 6 47.97 50.44 43.31 Mishraq Sulphur 6 43.68 49.19 38.48 North Fertilizer Plant 10 44.27 50.35 36.36 MST 5 97.53 103.49 91.53
  • 6. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 110 Table 2: summarized the measurement of radon concentration, the potential alpha energy concentration, the absorption effective dose exposure and the lung cancer cases per year per 106 person. Sample Code CRn (Bq/m3 ) PAEC (mWL) AEDE (mSv.y- 1 ) Lung Cancer/106 person Phosphate factory 112.69 12.2 2.68 48.244 Glasses factory 44.67 4.8 1.062 19.124 Ceramic factory 43.51 4.7 1.035 18.627 Detergent Chemicals 45.04 4.9 1.071 19.282 North Oil 47.97 5.2 1.141 20.536 Mishraq Sulphur 43.68 4.7 1.039 18.700 North Fertilizer Plant 44.27 4.8 1.053 18.952 MST 97.53 10.5 2.320 41.753 Table 3: A comparison of radon concentration in air in Bq/m3 for some countries Country CRn (Bq/m3 ) PAEC (mWL) AEDE (mSv/y) Ref. Iraq 103.98 17.2 2.47 Battawy and Hussein 13.53 - 51.176 -- -- Al-Gaim et al. Jordan 33.28 -- -- AL-Kofahi et al. 29.3 to 99.7 -- -- Abumurad et al. Hong Kong 48±32 5.2±5.1 -- Yu et al. Brazil 5 - 200 -- -- Magalhaes et al. Italy 5 - 15 -- 0.12 Magalhaes et al. Japan 6.1 -- 0.45 Oikawa et al. India Taj Mahal 213 -- 1.3 - 4.4 Kumar et al. Punjab 84.93 - 128.53 -- 1.45 - 2.19 Badhan et al. Garhwal and Kumaun 11 - 191 -- -- Ramola western Haryana 76 - 115.46 -- -- Kansal et al. Spain above 400 -- -- Sánchez, et al. Canada 41.9 -- -- Chen et al. Iraq 59.93 6.5 1.43 Present study
  • 7. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 111 Figure 1: The relation of radon concentration and track density in standard samples. Figure 2: Arrangement of the LR-115 detector of (1.5×1.5) cm2 placed in the outdoor air. The distance between the detectors and the ground level is 2.5 m.
  • 8. Journal of Environment and Earth Science www.iiste.org ISSN 2224-3216 (Paper) ISSN 2225-0948 (Online) Vol. 3, No.3, 2013 112 Figure 3: shows the histogram of radon concentration in factories 0 20 40 60 80 100 120 Phosphate factory Glasses factory Ceramic factory Detergent Chemicals North Oil Mishraq Sulphur North Fertilizer Plant MST CRn(Bq/m3) Factories