11 research outputs found

    Decontamination of Uranium-Polluted Groundwater by Chemically-Enhanced, Sawdust-Activated Carbon

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    The preparation of highly efficient and low-cost activated carbon from sawdust was achieved for the treatment of uranium-contaminated groundwater. The adsorption properties of the synthesized activated carbon, as well as their ability to be reused, were assessed. The obtained results demonstrated that sawdust activated carbon (SDAC) and its amine form (SDACA) had high affinity towards uranium ions at pH values of 4.5 and 5 for SDAC and SDACA, respectively. The experimental results showed that the maximum adsorption capacity of uranium was 57.34 and 76.7 mg/g for SDAC and SDACA, respectively. A maximum removal efficiency of 89.72% by SDAC and 99.55% by SDACA were obtained at a solid/liquid ratio of 8 mg/mL. The removal mechanism of uranium by SDAC and SDACA was suggested due to interaction with the amine and carboxylic groups. The validation of the method was verified through uranium separation from synthetic as well as from groundwater collected from water wells in the Wadi Naseib area, Southwestern Sinai, Egypt

    Sorption of Uranium Ions from Their Aqueous Solution by Resins Containing Nanomagnetite Particles

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    Magnetic amine resins composed of nanomagnetite (Fe3O4) core and glycidyl methacrylate (GMA)/N,N′-methylenebisacrylamide (MBA) shell were prepared by suspension polymerization of glycidyl methacrylate with N,N′-methylenebisacrylamide in the presence of nanomagnetite particles and immobilized with different amine ligands. These resins showed good magnetic properties and could be easily retrieved from their suspensions using an external magnetic field. Adsorption behaviors of uranium ions on the prepared resins were studied. Maximum sorption capacities of uranium ions on R-1 and R-2 were found to be 92 and 158 mg/g. Uranium was extracted successfully from three granite samples collected from Gabal Gattar pluton, North Eastern Desert, Egypt. The studied resins showed good durability and regeneration using HNO3

    Decontamination of Uranium-Polluted Groundwater by Chemically-Enhanced, Sawdust-Activated Carbon

    No full text
    The preparation of highly efficient and low-cost activated carbon from sawdust was achieved for the treatment of uranium-contaminated groundwater. The adsorption properties of the synthesized activated carbon, as well as their ability to be reused, were assessed. The obtained results demonstrated that sawdust activated carbon (SDAC) and its amine form (SDACA) had high affinity towards uranium ions at pH values of 4.5 and 5 for SDAC and SDACA, respectively. The experimental results showed that the maximum adsorption capacity of uranium was 57.34 and 76.7 mg/g for SDAC and SDACA, respectively. A maximum removal efficiency of 89.72% by SDAC and 99.55% by SDACA were obtained at a solid/liquid ratio of 8 mg/mL. The removal mechanism of uranium by SDAC and SDACA was suggested due to interaction with the amine and carboxylic groups. The validation of the method was verified through uranium separation from synthetic as well as from groundwater collected from water wells in the Wadi Naseib area, Southwestern Sinai, Egypt

    Appreciatively Efficient Sorption Achievement to U(VI) from the El Sela Area by ZrO<sub>2</sub>/Chitosan

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    The need to get uranium out of leaching liquid is pushing scientists to come up with new sorbents. This study uses the wet technique to improve the U(VI) sorption properties of ZrO2/chitosan composite sorbent. To validate the synthesis of ZrO2/CS composite with Zirconyl-OH, -NH, and -NH2 for U(VI) binding, XRD, FTIR, SEM, EDX, and BET are used to describe the ZrO2/chitosan wholly formed. To get El Sela leaching liquid, it used 150 g/L H2SO4, 1:4 S:L ratio, 200 rpm agitation speed, four hours of leaching period, and particle size 149–100 µm. In a batch study, the sorption parameters are evaluated at pH 3.5, 50 min of sorbing time, 50 mL of leaching liquid (200 mg/L U(VI)), and 25 °C. The sorption capability is 175 mg/g. Reusing ZrO2/CS for seven cycles with a slight drop in performance is highly efficient, with U(VI) desorption using 0.8 M acid and 75 min of desorption time. The selective U(VI) recovery from El Sela leachate was made possible using ZrO2/CS. Sodium diuranate was precipitated and yielded a yellow cake with a purity level of 94.88%

    Cellulose and chitosan derivatives for enhanced sorption of erbium(III)

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    International audienceCellulose (Cell) was chemically modified by grafting thiourea (Thio-Cell) and glutaraldehyde cross-linked chitosan (GLA-Chit) was functionalized by poly(aminocarboxymethylation) (PCM-Chit); material was also prepared as a composite material that incorporates a magnetic core (Magn PCM-Chit). The sorption properties of these materials have been compared to non-modified cellulose and GLA-Chit for Er(III) uptake. Sorption increases with progressive deprotonation of reactive groups, such as R-OH, R-SH, amine and carboxylic acid groups. The chemical modification significantly increases sorption performance and more specifically the poly (aminocarboxymethylation): sorption capacities increase up to 117-145 mg Er(III) g(-1). Sorption capacities also increase with temperature: the sorption is endothermic and spontaneous. The spontaneity of the reaction significantly increases with chemical modification of chitosan-based sorbent. The entropy of the system is negative for GLA-Chit, Cell and Thio-Cell and positive for PCM-Chit materials. Acidic solutions of thiourea efficiently desorb Er(III) and allows the recycling of the sorbents for a minimum of 5 sorption/desorption cycles. FT-IR spectrometry, XRD, TGA, elemental analyses and SEM observations have been used for characterizing the materials. The magnetic properties of Magn PCM-Chit were also characterized by VSM

    Kinetics and Thermodynamics Studies on the Recovery of Thorium Ions Using Amino Resins with Magnetic Properties

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    Magnetic polymeric matrixces were synthesized from glycidyl methacrylate, <i>N</i>,<i>N</i>′-methylenebis­(acrylamide) (MBA), and nanomagnetite particles. The obtained polymers were modified by ethylenediamine (DA) and diethylenetriamine (TA) to produce two amino-magnetic resins named R-DA and R-TA. The recovery of Th­(IV) ions from their aqueous solutions by R-DA and R-TA were studied in the pH range 1–4. Maximum adsorption capacity values of 60 and 84 mg/g of Th­(IV) ions on R-DA and R-TA, respectively, were obtained at pH 3.5 and 293 K. At a solid/liquid ratio (S/L) of 2 g/L, recovery efficiency values of 86 and 95% were achieved from initial thorium ion concentration of 100 mg/L using R-DA and R-TA, respectively. Adsorption isotherms and kinetic and thermodynamic parameters of the adsorption process were obtained and analyzed. Regeneration of the resins was tested by eluting the loaded Th­(IV) ions on the spent resins using 0.2 M HNO<sub>3</sub> followed by washing with dilute NaOH
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