<p>Adsorption is one of the most widely methods due to inexpensive and eco-friendly nature. In this context a novel composite was produced through in situ chemical polymerization of aniline on the surfaces of NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> particles. The analytical techniques such as Fourier transform infrared spectroscopy, X-ray diffraction, BET and Scanning Electron Microscopy were used to analyze the structure of the investigated material. The BET analysis revealed that polyaniline@NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> exhibited a specific surface area of 16.17 m<sup>2</sup>/g and contained a pore volume measuring of 0.069 m<sup>3</sup>/g. FTIR analysis revealed characteristic bands of both polyaniline and NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub>, confirming the successful polymerization of polyaniline on the NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> surface. The experimental results demonstrated a remarkable performance in removing Orange G from aqueous medium, achieving an optimal removal efficiency of 94.39%. This result was obtained after 25&#xa0;min of agitation under precisely controlled conditions: a solution pH maintained at 5.45, adsorbent dose fixed at 0.5&#xa0;g·L<sup>−1</sup> and an initial OG concentration of 20&#xa0;ppm. Equilibrium isotherm modeling revealed that the adsorption of OG dye on the polyaniline@NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> adsorbents was well fitted with Langmuir model, showing a maximum adsorption capacity of 126&#xa0;mg/g. The adsorption kinetics of the system were effectively described by a pseudo-second-order model in comparison to other kinetic models. The process of OG being adsorbed onto polyaniline@NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> occurs spontaneously through an endothermic reaction. Demonstrating that the prepared composite has a high outstanding adsorption property. The main adsorption mechanisms facilitating the removal of this azo dye by polyaniline@NaPO<sub>3</sub>-Fe<sub>2</sub>O<sub>3</sub> include π—π interactions, hydrogen bonding, and electrostatic attraction.</p>

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Sustainable Removal of Orange G from Aqueous Solutions Using PANI@coacervate Composite: Adsorption and Performance

  • Amina Rguibi,
  • Driss Rair,
  • Abdelghani Hsini,
  • Abdelillah Shaim,
  • Touriya Jermoumi,
  • Abdelkrim Chahine

摘要

Adsorption is one of the most widely methods due to inexpensive and eco-friendly nature. In this context a novel composite was produced through in situ chemical polymerization of aniline on the surfaces of NaPO3-Fe2O3 particles. The analytical techniques such as Fourier transform infrared spectroscopy, X-ray diffraction, BET and Scanning Electron Microscopy were used to analyze the structure of the investigated material. The BET analysis revealed that polyaniline@NaPO3-Fe2O3 exhibited a specific surface area of 16.17 m2/g and contained a pore volume measuring of 0.069 m3/g. FTIR analysis revealed characteristic bands of both polyaniline and NaPO3-Fe2O3, confirming the successful polymerization of polyaniline on the NaPO3-Fe2O3 surface. The experimental results demonstrated a remarkable performance in removing Orange G from aqueous medium, achieving an optimal removal efficiency of 94.39%. This result was obtained after 25 min of agitation under precisely controlled conditions: a solution pH maintained at 5.45, adsorbent dose fixed at 0.5 g·L−1 and an initial OG concentration of 20 ppm. Equilibrium isotherm modeling revealed that the adsorption of OG dye on the polyaniline@NaPO3-Fe2O3 adsorbents was well fitted with Langmuir model, showing a maximum adsorption capacity of 126 mg/g. The adsorption kinetics of the system were effectively described by a pseudo-second-order model in comparison to other kinetic models. The process of OG being adsorbed onto polyaniline@NaPO3-Fe2O3 occurs spontaneously through an endothermic reaction. Demonstrating that the prepared composite has a high outstanding adsorption property. The main adsorption mechanisms facilitating the removal of this azo dye by polyaniline@NaPO3-Fe2O3 include π—π interactions, hydrogen bonding, and electrostatic attraction.