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Mitigation and Remedy of Groundwater Arsenic Menace in India

Mitigation and Remedy of Groundwater Arsenic Menace in India

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<strong>Mitigation</strong> <strong>and</strong> <strong>Remedy</strong> <strong>of</strong> <strong>Groundwater</strong> <strong>Arsenic</strong> <strong>Menace</strong> <strong>in</strong> <strong>India</strong> : A Vision Documentat the benefits <strong>of</strong> water wells that pump from depths where the water is less contam<strong>in</strong>ated. Theauthors showed that by <strong>in</strong>stall<strong>in</strong>g wells to depths >150 m <strong>and</strong> us<strong>in</strong>g that water only forhouseholds could provide 90% <strong>of</strong> the region with low-arsenic water for 1,000 years. Water forirrigation would cont<strong>in</strong>ue to be taken from near the surface because us<strong>in</strong>g the deep aquifers forboth purposes could stress the resource, potentially draw<strong>in</strong>g surface arsenic <strong>in</strong>to the deeperreservoirs. Simulations provided two explanations: deep domestic pump<strong>in</strong>g would slightly perturbthe deep groundwater flow system, while substantial shallow pump<strong>in</strong>g for irrigation would forma hydraulic barrier for protect<strong>in</strong>g deeper resources from shallow arsenic sources. The analysis,further, <strong>in</strong>dicated that this simple management approach could provide arsenic-free dr<strong>in</strong>k<strong>in</strong>gwater to >90% <strong>of</strong> the arsenic-impacted region for a period over 1,000-year.Paul <strong>and</strong> Sikdar (2008) carried out numerical model<strong>in</strong>g <strong>of</strong> groundwater arseniccontam<strong>in</strong>ation movement for the English Bazar Block, Malda District, West Bengal. The study<strong>in</strong>dicated that high abstraction <strong>of</strong> groundwater because <strong>of</strong> irrigation requirement has led to bothhorizontal <strong>and</strong> downward vertical movement <strong>of</strong> arsenious water with<strong>in</strong> the aquifer towards thefresh water zones. The pattern <strong>of</strong> path-l<strong>in</strong>es <strong>of</strong> groundwater flow was del<strong>in</strong>eated quite differentfrom the pre-development case. It was recommended from the above studies that if theabstraction rate is <strong>in</strong>creased to 100m3/hr then with<strong>in</strong> 50 years, there is a possibility <strong>of</strong> the aquifergett<strong>in</strong>g contam<strong>in</strong>ated but if the rate is decreased to 30m3/hr then the aquifer may rema<strong>in</strong>uncontam<strong>in</strong>ated at least for the next 50 years.There are several other groundwater arsenic model<strong>in</strong>g studies. The po<strong>in</strong>ts primarilyadvocated <strong>in</strong> most <strong>of</strong> the model<strong>in</strong>g studies are: (i) sources <strong>of</strong> arsenic <strong>in</strong> groundwater system are<strong>in</strong>-situ <strong>and</strong> <strong>in</strong> localized patches, <strong>and</strong> their mobilization is governed by exploitation <strong>of</strong> the groundwaterregime, (ii) by adopt<strong>in</strong>g judicious aquifer management, arsenic free groundwater can betapped for a long period with no risk <strong>of</strong> perturb<strong>in</strong>g arsenic contam<strong>in</strong>ated zones, <strong>and</strong> (iii) tapp<strong>in</strong>g <strong>of</strong>deep uncontam<strong>in</strong>ated aquifer <strong>and</strong> freshwater zones <strong>in</strong> conjunction with surface water sourcemay ensure supply <strong>of</strong> arsenic free water both for dr<strong>in</strong>k<strong>in</strong>g <strong>and</strong> agricultural requirement.3.6 Chemical processes <strong>of</strong> arsenic contam<strong>in</strong>ationAlthough there are number <strong>of</strong> hypotheses expla<strong>in</strong><strong>in</strong>g chemical processes groundwaterarsenic contam<strong>in</strong>ation, however, the most commonly believed chemical processes are dissolution.Iron arsenate (FeAsO 4) may be tentatively regarded as the direct <strong>and</strong> immediate source<strong>of</strong> arsenic, because it is easily formed from scorolite [FeAs 4, 2H 2O] <strong>and</strong> pitticite (hydratedmixture <strong>of</strong> arsenate <strong>and</strong> sulphate), that are common alternation products <strong>of</strong> arsenopyrite. S<strong>in</strong>cearsenopyrite can conta<strong>in</strong> As (III) ions <strong>in</strong> small proportion with ions <strong>of</strong> As (V), which is thedom<strong>in</strong>ant constituent, it is quite likely that arsenic <strong>in</strong> the alluvium occurs as ferric arsenate (FeAsO 4),with ferric arsenite (FeAsO 3) <strong>in</strong> m<strong>in</strong>or proportion. Due to hydrolysis under conditions <strong>of</strong> low pH<strong>and</strong> high Eh, ferric arsenate is dissociated <strong>in</strong>to the strongly poisonous arsenic acid (H 3AsO 4)NIH & CGWB 49

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