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Kinetic, isotherm and thermodynamic investigations of Cu2+ adsorption onto magnesium hydroxyapatite/ferroferric oxide nano-composites with easy magnetic separation assistance

✍ Scribed by Cui, Limei; Hu, Lihua; Guo, Xiaoyao; Zhang, Yakun; Wang, Yaoguang; Wei, Qin; Du, Bin


Book ID
126491084
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
780 KB
Volume
198
Category
Article
ISSN
0167-7322

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✦ Synopsis


A novel magnetic nano-composite was synthesized by a simple method of coprecipitation through embedding ferroferric oxide into magnesium hydroxyapatite (MgHAp/Fe3O4) to remove Cu2+ from aqueous solution. The obtained adsorbent was characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), Brunauer–Emmett–Teller (BET) surface area measurement and Fourier transform infrared spectroscopy (FTIR). Mg2+ and Cu2+ possess the same electrical charge and similar ionic radius, which is especially beneficial to their exchange in hydroxyapatites. Static adsorption experiments indicated that the maximal immobilization capacity of Cu2+ reached to 305mg/g on the optimum adsorption conditions (dosage of 0.32mg/mL, contact time for 90min, pH at 5.9 and temperature at 25°C). Adsorption kinetics including the pseudo-first order and pseudo-second order kinetic models were researched and the data fitted better with the pseudo-second order kinetic model (R
2
=0.99). For adsorption isotherms, Freundlich isotherm was proved to be the best correlation (R
2

0.99) compared with the Henry and Langmuir isotherms. The thermodynamic parameters (ΔG
<0, ΔS
=43.38J/mol/K, ΔH
=7.006kJ/mol) indicated that it was a spontaneously endothermic reaction. Furthermore, the well anti-interference and stability properties of the MgHAp/Fe3O4 adsorbent were confirmed through the interference experiment of coexistent metal cations and desorption experiment, respectively.


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