Towards the development of a reactive filter from green resource for groundwater defluoridation

Preparation of a reactive filter from green resource for groundwater defluoridation. [Display omitted] •Transformations of CaCO3 to CaO enhanced the defluoridation efficiency of TGS.•pH, organic load and ionic strength had no influence on the defluoridation efficiency.•Only carbonate impacted negati...

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Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2016-10, Vol.301, p.166-177
Hauptverfasser: Oladoja, N.A., Helmreich, B., Bello, H.A.
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Helmreich, B.
Bello, H.A.
description Preparation of a reactive filter from green resource for groundwater defluoridation. [Display omitted] •Transformations of CaCO3 to CaO enhanced the defluoridation efficiency of TGS.•pH, organic load and ionic strength had no influence on the defluoridation efficiency.•Only carbonate impacted negative on the defluoridation efficiency.•The underlying defluoridation mechanisms were diverse and not straitlaced.•GW defluoridation altered some physicochemical characteristics of the product water. In order to develop a low cost reactive filter from a green biogenic resource, the shell of a Gastropod (GS) was calcined at different temperatures and the defluoridation efficiencies of the raw and calcined GS were evaluated in a batch process. The highest defluoridation efficiency was obtained with the GS calcined at 1000°C (i.e. TGS1000). The time–concentration profiles of the defluoridation process were described by the pseudo-second order kinetic equation and the Temkin equilibrium isotherm equation gave the best description of the defluoridation process in synthetic feed water and groundwater (GW) system. The determination of the effects of hydrochemistry on the defluoridation efficiency of the TGS1000 showed that variations in pH value, organic load and ionic strength had no visible influence on the magnitude and trend. Amongst the array of interfering ionic species studied, only carbonate exhibited negative impact on the defluoridation efficiency. Experimental evidences revealed that the underlying mechanisms of the defluoridation process were diverse (ionic bond formation, electrostatic attraction, ion exchange and occlusion into Ca(OH)2 framework) and not straitlaced. Groundwater (GW) defluoridation, using TGS1000, showed that the residual F− in the defluoridated water increased with initial F− concentration. The value of the monolayer Langmuir sorption capacity was lower in the GW system (qm=6.17mg/g) than in the synthetic feed water system (qm=19.84mg/g). The values of pH, electrical conductivity, Ca2+ concentrations, total hardness values were higher in the defluoridated water relative to the raw GW samples. The Mg2+ concentrations were below the detection limit and nitrate concentrations were appreciably attenuated in the treated water samples.
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[Display omitted] •Transformations of CaCO3 to CaO enhanced the defluoridation efficiency of TGS.•pH, organic load and ionic strength had no influence on the defluoridation efficiency.•Only carbonate impacted negative on the defluoridation efficiency.•The underlying defluoridation mechanisms were diverse and not straitlaced.•GW defluoridation altered some physicochemical characteristics of the product water. In order to develop a low cost reactive filter from a green biogenic resource, the shell of a Gastropod (GS) was calcined at different temperatures and the defluoridation efficiencies of the raw and calcined GS were evaluated in a batch process. The highest defluoridation efficiency was obtained with the GS calcined at 1000°C (i.e. TGS1000). The time–concentration profiles of the defluoridation process were described by the pseudo-second order kinetic equation and the Temkin equilibrium isotherm equation gave the best description of the defluoridation process in synthetic feed water and groundwater (GW) system. The determination of the effects of hydrochemistry on the defluoridation efficiency of the TGS1000 showed that variations in pH value, organic load and ionic strength had no visible influence on the magnitude and trend. Amongst the array of interfering ionic species studied, only carbonate exhibited negative impact on the defluoridation efficiency. Experimental evidences revealed that the underlying mechanisms of the defluoridation process were diverse (ionic bond formation, electrostatic attraction, ion exchange and occlusion into Ca(OH)2 framework) and not straitlaced. Groundwater (GW) defluoridation, using TGS1000, showed that the residual F− in the defluoridated water increased with initial F− concentration. The value of the monolayer Langmuir sorption capacity was lower in the GW system (qm=6.17mg/g) than in the synthetic feed water system (qm=19.84mg/g). The values of pH, electrical conductivity, Ca2+ concentrations, total hardness values were higher in the defluoridated water relative to the raw GW samples. The Mg2+ concentrations were below the detection limit and nitrate concentrations were appreciably attenuated in the treated water samples.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cej.2016.04.150</doi><tpages>12</tpages></addata></record>
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subjects Arrays
Calcination
Calcium rich materials
Defluoridation
Fluoride
Gastropod shell
Gastropoda
Groundwater
Ion exchange
Mathematical analysis
Raw
Roasting
Synthetic feeds
title Towards the development of a reactive filter from green resource for groundwater defluoridation
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