Application of calcium alginate-PANI@sawdust wood hydrogel bio-beads for the removal of orange G dye from aqueous solution.

This work aims to investigate the adsorption performance of orange G (OG) dye from aqueous solutions employing PANI@sawdust biocomposite enrobed by calcium-alginate bio-beads (Alg-PANI@SD). The as-prepared adsorbent was characterized by scanning-electron-microscopy (SEM), X-ray energy-dispersive spectroscopy (EDS), and Fourier transforms infrared (FT-IR) spectroscopy and used to remove orange G dye from aqueous water. Batch tests were performed as a function of adsorbent dosage, pH, contact time, interfering ions, and initial OG dye concentration. Experimental results show that the kinetic model of pseudo-first-order (PFO) and Freundlich isotherm perfectly fit the entire experimental data. Additionally, the prepared composite exhibited an excellent regeneration capacity and reusability for OG dye removal. The results revealed that the as-prepared Alg-PANI@SD bio-beads have the potential to be applied as a low-cost adsorbent for the adsorption of OG dye from aqueous media.

Effectiveness of a novel polyaniline@Fe-ZSM-5 hybrid composite for Orange G dye removal from aqueous media: Experimental study and advanced statistical physics insights.

A polyaniline@Fe-ZSM-5 composite was synthesized via an in situ interfacial polymerization procedure. The morphology, crystallinity, and structural features of the as-developed PANI@Fe-ZSM-5 composite were assessed using scanning electron microscopy - energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). The composite was efficiently employed for the first time as an adsorbent Orange G (OG) dyestuff from water. The OG dye adsorption performance was investigated as a function of several operating conditions. The kinetic study demonstrated that a pseudo-second-order model was appropriate to anticipate the OG adsorption process. The maximum adsorption capacity was found to be 217 mg/g. The adsorption equilibrium data at different temperatures were calculated via advanced statistical physics formalism. The entropy function indicated that the disorder of OG molecules improved at low concentrations and lessened at high concentrations. The free enthalpy and internal energy functions suggested that the OG adsorption was a spontaneous process and physisorption in nature. Regeneration investigation showed that the PANI@Fe-ZSM-5 could be effectively reused up to five cycles. The main results of this work provided a deep insight on the experimental study supported by advanced statistical physics prediction for the adsorption of Orange G dye onto the novel polyaniline@Fe-ZSM-5 hybrid composite. Additionally, the experimental and advanced statistical physics findings stated in this study may arouse research interest in the field of wastewater treatment.

Efficient removal of crystal violet dye from aqueous solutions using sodium hydroxide-modified avocado shells: kinetics and isotherms modeling.

The main objective of this study is to optimize a new composite for the depollution of contaminated water. The sodium hydroxide-modified avocado shells (NaOH-AS) were firstly prepared, characterized by field-emission-scanning-electron-microscopy (FE-SEM), X-ray energy dispersive spectroscopy (EDS) and Fourier transforms infrared (FT-IR) spectroscopy, and applied for efficient removal of crystal violet dye (CV) in wastewater. In addition, the adsorption in a batch system of CV dye on the NaOH-AS material was studied. Therefore, we accomplished a parametric study of the adsorption by studying the effect of several important parameters on the decolorizing power of the used material, namely, initial pH, contact time, initial CV dye concentration, temperature, and the ionic strength effect on the CV dye adsorption process were systematically assessed. The highest adsorption efficiency of CV dye (>96.9%) by NaOH-AS was obtained at pH >8. The pseudo-second-order kinetic model gave the best description of the adsorption kinetic of CV dye on the AS and NaOH-AS adsorbents. In addition, the mass transfer of CV dye molecules from the solution to the adsorbent surface occurred in three sequential stages (boundary layer diffusion, intraparticle diffusion and adsorption equilibrium). The adsorption isotherm data were best fitted with the Freundlich model. The adsorption capacity of AS increased from 135.88 to 179.80 mg g-1 after treatment by 1 M NaOH. The thermodynamic study showed that CV dye adsorption onto NaOH-AS was an exothermic and feasible process. The electrostatic interactions acted as the only forces governing the CV adsorption mechanism. The NaOH-AS demonstrated a satisfactory reusability. Therefore, we can state that the as-developed NaOH-AS material has a potential application prospect as an efficient adsorbent for CV dye from wastewaters.

Efficient detoxification of Cr(VI)-containing effluents by sequential adsorption and reduction using a novel cysteine-doped PANi@faujasite composite: Experimental study supported by advanced statistical physics prediction.

Nowadays, the global spreading of hazardous heavy metals becomes a top-priority environmental challenge, owing to its serious detrimental health outcomes. Herein, a novel cysteine-doped polyaniline@faujasite hybrid composite (Cys-PANi@FAU-50) was synthesized via a facile in-situ polymerization route for the effective detoxification of Cr(VI)-bearing wastewaters. The Cys-PANi@FAU-50 composite displayed an open mesoporous structure richly decorated with nitrogen/oxygen-containing functional groups, which consequently boosted the diffusion, adsorption and reduction of Cr(VI) oxyanions. The Cr(VI) adsorption behavior was satisfactorily tailored via pseudo-second-order law and Langmuir model with a maximum uptake capacity of 384.6 mg/g. Based on the advanced statistical physics theory, the monolayer model with two distinct receptor sites provided a reliable microscopic and macroscopic prediction of the Cr(VI) adsorption process. Stereographically, the Cr(VI) ions were adsorbed through horizontal multi-anchorage and vertical multi-molecular mechanisms on the amine and hydroxyl groups of Cys-PANi@FAU-50, respectively. The thermodynamic functions evidenced that the Cr(VI) adsorption was an endothermic spontaneous process. XPS analysis proved that Cr(VI) ions were electrostatically adsorbed, and subsequently reduced to Cr(III), which were in turn immobilized by chelation with imine/sulfonate groups and electrostatic interactions with carboxylate groups. The Cys-PANi@FAU-50 featured an effortless regenerability and good reusability. Overall, the Cys-PANi@FAU-50 composite owns outstanding potentiality for detoxifying Cr(VI)-laden effluents.

Polyaniline coated tungsten trioxide as an effective adsorbent for the removal of orange G dye from aqueous media.

In this work, the core-shell PANI@WO3 composite was obtained from the reaction of aniline monomer polymerization with WO3 particles; sodium persulfate was used as an oxidant. Various analytical techniques such as scanning electron microscopy (SEM-EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS) were used to characterize the as-prepared PANI@WO3 adsorbent, which well confirmed that the WO3 particles were coated by polyaniline polymer. The PANI@WO3 composite was tested as an adsorbent to remove reactive orange G (OG) for the first time. pH, adsorbent dose, contact time, initial dye concentration, and temperature were systematically investigated in order to study their effect on the adsorption process. The experimental findings showed that the PANI@WO3 composite has considerable potential to remove an aqueous OG dye. Langmuir and Freundlich's models were used to analyze the equilibrium isotherms of OG dye adsorption on the PANI@WO3 composite. As a result, the best correlation of the experimental data was provided by the Langmuir model, and the maximum capacity of adsorption was 226.50 mg g-1. From a thermodynamic point of view, the OG dye adsorption process occurred spontaneously and endothermically. Importantly, PANI@WO3 still exhibited an excellent adsorption capability after four regeneration cycles, indicating the potential reusability of the PANI@WO3 composite. These results indicate that the as prepared PANI@WO3 composite could be employed as an efficient adsorbent and was much better than the parent material adsorption of OG dye.