search
for
 About Bioline  All Journals  Testimonials  Membership  News


International Journal of Environment Science and Technology
Center for Environment and Energy Research and Studies (CEERS)
ISSN: 1735-1472 EISSN: 1735-2630
Vol. 3, Num. 4, 2006, pp. 447-453

International Journal of Enviornmental Science and Technology, Vol. 3, No. 4, Autumn 2006, pp.447-453

Slow arsenic poisoning of the contaminated groundwater users

1*M. M., Uddin, 2A. K. M., Harun-Ar-Rashid, 3S. M., Hossain, 3M. A., Hafiz, 3K. Nahar and 3S. H. Mubin

1Department of Physics, Chittagong University of Engineering and Technology, Chittagong, Bangladesh
2Department of Physics, University of Chittagong, Chittagong, Bangladesh
3Institute of Nuclear Science and Technology, Atomic Energy Research Establishment, Dhaka, Bangladesh
*Corresponding author, Email:mohi@cuet.ac.bd Tel.: +88031 714 947; Fax: +88031 714 910

Received 9 March 2006
Accepted 7 September 2006

Code Number: st06054

ABSTRACT: This paper gives impact of Arsenic contaminated water on human health as well as overview of the extent and severity of groundwater arsenic contamination in Bangladesh. Scalp hair is the most important part of the human body to monitor the accumulation of this type of poison. Therefore, an experiment has been carried out by Neutron Activation Analysis (NAA) at Atomic Energy Research Establishment (AERE), Savar, Dhaka, Bangladesh on human hair of corresponding tube well water users of these areas to determine the total accumulation of arsenic to their body. Hair samples collected from the region where the groundwater was found highly contaminated with arsenic. The obtained results of arsenic concentration in the lower age (Hb) categories of users (below 12 years of age users) is in the range of 0.33 to 3.29 µg/g (ppm) and that in the Hu categories (upper 12 years of age users) is 0.47 to 6.64 µg/g (ppm). Where as maximum permissible range is 1 ppm certified from WHO. Results show that the peoples are highly affected where the groundwater is highly contaminated with arsenic and acts as the primary source of arsenic poisoning among the peoples of those areas. The results indicate that human population is affected with arsenic locally using the contaminated water for a long time.

Key words: Arsenic, groundwater, Bangladesh, gamma ray activity, neutron activation analysis, trace elements

INTRODUCTION

Arsenic is one of the most commonly studies trace Toxic, naturally occurring arsenic species elements as it is both toxic and carcinogenic (Nriago,1994). It is reported that 40 % of arsenic in human body comes from food chain (BIAM, 2002). Arsenic has been taken into account as a dangerous environmental pollution and detected as a serious health risk in many countries of the world, reported from Argentina, Mexico, Chile, USA, Taiwan, Mongolia, Thailand, Philippines, China, Japan, India, as well as Bangladesh (Akram, 1997, BGS, 2001 and SOES-DCH, 2000). The arsenic contamination is not only a health hazard for the people; it also affects the environment Metabolic by products of arsenic V and creates social problems (Table 1). There are two main theories (Pyrite oxidation and oxyhydroxide reduction) as to how arsenic is released into the ground water.

Table 2

MATERIALS AND METHODS

Study area

Feni district of Bangladesh is selected for this experiment. It has six upazila. Each upazila comprises of several Unions. Each Union has some ‘blocks’ (wards). In each ‘blocks’ there are some ‘Villages’.

Fig. 1, Fig. 2

Sample collection

Hair samples were collected from the tube well water users. Hair samples of the water users of this district have been categorized into two: below 12 years of ages and upper 12 years and are coded as Hb and Hu, respectively. Before, collecting samples, scissor was cleaned by acetone to avoid the others contamination.

Sample preparation

Hair samples were transferred from polyethylene bag to the Petri dish. In order to clean hair samples properly, samples were washed and dried in the following ways;

i) Acetone and dried naturally
ii) Deionized water and then dried
iii) Again by acetone and dried

The dried clean hairs were cut into small pieces. Four types of standard reference materials were used for the analysis of two sets of hair samples (a total of 30 samples) supplied by National Institute of Standard and Technology (NIST). Whereas the first set was analyzed using the International Atomic Energy Agency (IAEA) certified reference materials Soil-7 and SL-1, the second set was analyzed using coal fly ash and pond sediment. About 100 mg hair was taken into the bullet type irradiation vial. The identification of the sample was put at the outer surface of the vial and heat-sealed.

Irradiation and data counting

Al-Au Flux monitors were used between the two set of samples to determine neutron flux gradients. The samples and standards were irradiated in the 3 MW TRIGA MARK-II research reactors at the Atomic Energy Research Establishment (AERE), Savar, and Dhaka, Bangladesh. The irradiation was performed with neutron flux of 1.52 × 1013 n/cm2/sec at a power level of 500 kW for 20 min. using Dry Central Thimble (DCT) facility, counting time for hair was 3600 sec. Below Fig. 3 show the irradiation capsule, get ready for irradiation.

After irradiation completes the samples, standards and flux monitors were counted with a high purity germanium detector coupled with a personal computer based S-100 Multi Channel Analyzer (MCA) master board packages. The energy spread in multichannel analyzer was adjusted to 0-1500 keV over 4096 channels.

Gammaraycounting wereperformed for samples and standards after a decay time of1-2 day, with a measuring time of 500-3600s for the determination of As [75As(n,γ)76As→76Se (t½ = 26.3 h; Eγ = 559.1 keV)]. Countings for flux monitors were performed with a measuring time of 60s for the determination of Au [197Au(n,γ)198Au(t½ = 2.35 d; Eγ = 411.6 keV)]. The dead time was kept below 7% during counting for both samples and standard.

Calculation of arsenic concentration

For the calculation of concentrations, the peakgr10 software package was used. Concentratrions calculation were also performed manually by the following activation equation

Where, ‘a’ and ‘b’ are the weight of the element in the sample and standard respectively. Ax* is the activityin sample and standard (Laul 1979).Both the program and manual calculations gave the consistent results.

Accuracy of the analysis and the total uncertainty

Quality Assurance (QA) test is performed to investigate the reliability of the analysis by measuring arsenic concentration level in standard reference materialsAs (NIST, USA), coal fly ash, SL-1and Soil-7 (IAEA) relative to primary standard of arsenic. The analytical results for certified reference materials are given in the table below. The experimental results are within 10% deviation, which is a good agreement with the certified value. This deviation was achieved due to poor counting statistics. Uncertainties of the samples were calculated according to the 1993 ISO guide and were added to the uncertainty in the measurement (Kuèera, et al., 1999). Table 3 Shows that Comparison of arsenic concentration determined in the standard reference material As (NIST, USA), Coal FlyAsh, Pond Sediment (NIST, USA), and SL-1, Soil-7, (IAEA) with the certified value.

RESULTS

The obtained results of arsenic concentration in the lower age Hb (below 12 years of age users) categories of users is in the range of 0.33 to 3.29 µg/g and that in the Hu (upper 12 years of age users) categories is in the range of 0.47 to 6.64 µg/g . Arsenic detected in the samples Hb-1 to Hb-6 is in the range of 0.13 to 3.29 µg/ g , where as arsenic in corresponding upper age users samples Hu-1 to Hu-6 is in the range of 1.48 to 6.64 µg/ g . Arsenic in the samples Hb-7 to Hb-14 is in the range of 0.33 to 1.2 µg/g , where as in corresponding upper age users samples Hu-7 to Hu-14 is in the range of 0.24 to 5.75 µg/g. Maximum permissible range of arsenic in the human scalp hair is 1 µg/g certified by WHO.

DISCUSSION AND CONCLUSION

In this study, arsenic is detected to the human scalp hair samples for both the Hb and Hu categories. It is shown in Fig. 4 that arsenic is detected in human scalp hair for both the Hb (below 12 years users) and Hu (Upper 12 years users) categories, but from the above Figs it is shown that the under 12 years old peoples (Hb) are less affected compared to the more than 12 years old peoples (Hu). From Fig. 4, it is shown that the samples Hb-1 to Hb-6, which were collected from the areas of the Sonagazi, Dagon bhuiyan Upazilas of the district, show and lower accumulation of arsenic where as from Fig. 4, the samples Hu-1 to Hu-11 show the higher accumulations. Hair samples Hb-7 to Hb-12 show very high accumulation of arsenic and the groundwater in the corresponding areas were found highly contaminated by arsenic and is in the range (110-190) mg/L (Uddin, et al., 2005). Hair samples Hb13 to Hb-14 in the under 12 years category show the lower accumulations of arsenic (0.45-0.63)µg/g which is justified to the corresponding lower arsenic found in the groundwater in the respective areas and is in the range (5-43) µg/g (Uddin, et al., 2005). Results were obtained from the experiment that the human hair samples, the fewer than 12 years old users (Hb) are less affected compared to the more than 12 year old users (Hu).

Therefore, it is concluded that higher values of arsenic in hair samples were due to the longtime accumulation of arsenic through the uses of contaminated groundwater. Results show that the ground water is contaminated with arsenic and acts as the primary source of arsenic poisoning among the peoples of those areas. The results indicate that human population is affected with arsenic locally using the contaminated water for a long time.

ACKNOWLEDGEMENT

This work was partly supported by National Institute of Standard and Technology (NIST), USA and International Atomic Energy Agency (IAEA).

REFERENCE

  • Akram, S., (1997). Arsenic problem. The daily sangbad of Bangladesh.
  • BGS, (1999). Ground water Studies for Arsenic Contamination in Bangladesh. Main Report and Supplemental, Dhaka, British Geological Survey, Bangladesh and Mott MacDonald International Ltd., United Kingdom: Government of the Peoples Republic of angladesh, Ministry of Local Government, Rural Development and Cooperatives, Department of Public Health Engineering. 1-3.
  • BGS (British Geological Survey), (2001). Ground water studies of arsenic contamination in Bangladesh. Phase 2, Nottingham, Britain.(British Geological Survey)
  • BIAM, (2002). 4th inernational conference on Arsenic contamination of underground water in Bangladesh cause, Effect and Remedy, Dhaka.
  • Karim, M. A., Komori, Y. and Alam, M., (1997). Subsurface Arsenic Occurrence and Depth of Contamination in Bangladesh. J. Environ. Chem., 7 (4), 783–792.
  • Kucera, J., Bode, P., and Stepanek, V., (1999). The 1993 ISO guide to the expression of uncertainty in measurement applied to NAA. J. Rad. Ana. Nuc. Chem., 245 (1), 15.
  • Laul, J. C., (1979). Atomic Energy Review. 17, 3. Nriago, J. O., (1994). Arsenic in the environment. 1, 52.
  • SOES-DCH. (2000). Groundwater Arsenic Contamination in Bangladesh. A. Summary of 239 days field survey from August 1995 to February 2000, B. Twenty-seven days detailed field survey information from April 1999 to February 2000. School of Environmental Studies, Jadavpur University, Calcutta 700 032, India and Dhaka Community Hospital, Dhaka 1217, Bangladesh.
  • Uddin, M. M., Harun-Ar-Rashid, A. K. M., and Hossain, S. M., (2005). Precise measurement of Arsenic in the Contaminated Groundwater of Bangladesh. Res. J. Mech. Eng., 5, 15-19.

© 2006 Center for Environment and Energy Research and Studies (CEERS)


The following images related to this document are available:

Photo images

[st06054f2.jpg] [st06054f3.jpg] [st06054f4.jpg] [st06054t1.jpg] [st06054t2.jpg] [st06054t3.jpg] [st06054f1.jpg]
Home Faq Resources Email Bioline
© Bioline International, 1989 - 2024, Site last up-dated on 01-Sep-2022.
Site created and maintained by the Reference Center on Environmental Information, CRIA, Brazil
System hosted by the Google Cloud Platform, GCP, Brazil