摘要

The magnetic, nanocrystalline Fe-0.2(Co20Ni80)(0.8) alloy porous microfibers were prepared by the citrate gel thermal decomposition and reduction process. The morphology, chemical composition, microstructure, and magnetic properties of the microfibers were investigated by X-ray diffraction, field emission scanning electron microscopy, energy-dispersive X-ray, Brunauere-Emmette-Teller, and vibration sample magnetometer. The as-prepared magnetic, nanocrystalline Fe-0.2(Co20Ni80)(0.8) porous microfibers consisting of about 48 nm grains are characterized by diameters of 1-4 mu m, specific surface area of 17.73 m(2)/g, and specific magnetization of 196.7 Am-2/kg. The arsenic(V) absorption on these magnetic Fe-0.2(Co20Ni80)(0.8) porous microfibers at room temperature was determined by the ICP-AES measurement of arsenic(V) in aqueous solution. The results show that the pseudo-first-order kinetic model is consistent with the arsenic(V) adsorption process and a good correlation coefficient (R (2) = 0.9862). By comparing among the Langmuir, Freundlich, Temkin, and Redlich-Peterson models for adsorption isotherms of arsenic(V) onto the magnetic Fe-0.2(Co20Ni80)(0.8) porous microfibers at room temperature, the Freundlich model and Redlich-Peterson model can be used to evaluate the arsenic(V) adsorption isotherm at room temperature. The arsenic(V) equilibrium absorbance of the magnetic Fe-0.2(Co20Ni80)(0.8) porous microfibers is up to 1.9 mg/g when the initial arsenic(V) concentration is 1.0 mg/L in aqueous solution.

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