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      Excellent fluoride removal performance by electrospun La–Mn bimetal oxide nanofibers

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          Abstract

          A novel La–Mn bimetal oxide nanofiber adsorbent was fabricated by the combination of an electrospinning approach and heat treatment in a simple strategy to remove fluoride ions from water.

          Abstract

          La–Mn bimetal oxide nanofibers, used as an adsorbent for the defluoridation of water, were synthesized by an electrospinning and heat treatment technology. The La–Mn bimetal oxide nanofiber adsorbent with a specific surface area of 35.064 m 2 g −1 displayed a good defluoridation performance. Both the adsorption kinetics and equilibrium for fluoride (F ) uptake onto La–Mn bimetal oxide nanofibers were investigated. The kinetic studies established that the adsorption attained equilibrium at about 90 min, and the PSO kinetic model was ideal for the kinetic data under 20 and 50 mg L −1. The Langmuir maximum F uptake was computed to be 189.39 mg g −1 at 308 K and pH 3. A thermodynamic study affirmed a feasible, endothermic, spontaneous and entropy driven process of F adsorption towards La–Mn bimetal oxide nanofibers at the studied temperature range. Except for the competitive adsorption of PO 4 3− and F , the presence of NO 3 , CO 3 2−, Cl and SO 4 2− had little effect on fluoride removal. The La–Mn bimetal oxide adsorbent exhibited a good reusability.

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          Is Open Access

          Synthesis and application of Granular activated carbon from biomass waste materials for water treatment: A review

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            Removal of phosphate from water by a Fe-Mn binary oxide adsorbent.

            Phosphate removal is important in the control of eutrophication of water bodies and adsorption is one of the promising approaches for this purpose. A Fe-Mn binary oxide adsorbent with a Fe/Mn molar ratio of 6:1 for phosphate removal was synthesized by a simultaneous oxidation and coprecipitation process. Laboratory experiments were carried out to investigate adsorption kinetics and equilibrium, in batch mode. The effects of different experimental parameters, namely contact time, initial phosphate concentration, solution pH, and ionic strength on the phosphate adsorption were investigated. The adsorption data were analyzed by both Freundlich and Langmuir isotherm models and the data were well fit by the Freundlich isotherm model. Kinetic data correlated well with the pseudo-second-order kinetic model, suggesting that the adsorption process might be chemical sorption. The maximal adsorption capacity was 36 mg/g at pH 5.6. The phosphate adsorption was highly pH dependent. The effects of anions such as Cl(-),SO42-, and CO32- on phosphate removal were also investigated. The results suggest that the presence of these ions had no significant effect on phosphate removal. The phosphate removal was mainly achieved by the replacement of surface hydroxyl groups by the phosphate species and formation of inner-sphere surface complexes at the water/oxide interface. In addition, the adsorbed phosphate ions can be effectively desorbed by dilute NaOH solutions. This adsorbent, with large adsorption capacity and high selectivity, is therefore a very promising adsorbent for the removal of phosphate ions from aqueous solutions.
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              Synchronous phosphate and fluoride removal from water by 3D rice-like lanthanum-doped La@MgAl nanocomposites

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                Author and article information

                Contributors
                Journal
                NJCHE5
                New Journal of Chemistry
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                January 04 2022
                2022
                : 46
                : 2
                : 490-497
                Affiliations
                [1 ]Fujian Key Laboratory of Eco-Industrial Green Technology, College of Ecology and Resources Engineering, Wuyi University, Wuyishan 354300, China
                [2 ]Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Materials Science and Engineering, Nanjing Forestry University, Nanjing, 210037, China
                [3 ]College of Mechanical and Electrical Engineering, Wuyi University, Wuyishan 354300, China
                Article
                10.1039/D1NJ04976C
                2756a438-c7ff-4c38-8f05-2ed71295ea82
                © 2022

                http://rsc.li/journals-terms-of-use

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