Development of a ghatti gum/poly (acrylic acid)/TiO2 hydrogel nanocomposite for malachite green adsorption from aqueous media: Statistical optimization using response surface methodology.

The primary goal of this study is to prepare and characterize a ghatti gum/poly(acrylic acid)/TiO2 (GG/poly(AA)/TiO2) hydrogel nanocomposite for adsorption of the dye malachite green (MG) from the aqueous phase in a discontinuous system. A variety of approaches were used to investigate the structure, morphology, and thermomechanical characteristics of the synthesized hydrogel nanocomposite. Response surface methodology (RSM) was performed to analyze the impact of three processing parameters, namely adsorbent dosage, dye concentration, contact duration, and their interactions on MG dye adsorption capacity. Analysis of variance was used to assess the experimental findings, which revealed that the quadratic regression model was statistically acceptable. The integration of TiO2 nanoparticles into the hydrogel matrix improved its thermal stability, mechanical strength, and performance in adsorbing MG dye from water. The kinetics and isotherm were evaluated, and the adsorption process was well fitted with pseudo-second order and Temkin isotherm models, respectively. Using the Langmuir equation, the maximum adsorption capacity at 45 °C within 50 min was calculated to be 2145 mg/g. Thermodynamic analysis at 25-45 °C revealed that the MG dye was spontaneously absorbed by the hydrogel nanocomposite. The prepared hydrogel nanocomposite demonstrated excellent reusability without a noticeable loss in MG dye adsorption capability for 6 cycles.

Synthesis and characterization of magnetic clay-based carboxymethyl cellulose-acrylic acid hydrogel nanocomposite for methylene blue dye removal from aqueous solution.

Carboxymethyl cellulose/poly(acrylic acid) (CMC-cl-pAA) hydrogel and its magnetic hydrogel nanocomposite (CMC-cl-pAA/Fe3O4-C30B) were prepared via a free radical polymerization method and used as adsorbents for adsorption of methylene blue (MB) dye. The samples were characterized using Fourier transform infrared, X-ray diffraction, thermogravimetric analysis, scanning electron microscopy coupled with energy-dispersive X-ray spectrometer, high-resolution transmission electron microscope, and dynamic mechanical analysis. The adsorption performance of the prepared adsorbents was studied in a batch mode. Adsorption kinetics and isotherm models were applied in the experimental data to evaluate the nature as well as the mechanism of adsorption processes. It was deduced that the adsorption followed the pseudo-second-order rate equation and Langmuir isotherm models. The maximum adsorption capacities were found to be 1109.55 and 1081.60 mg/g for CMC-cl-pAA hydrogel and CMC-cl-pAA/Fe3O4-C30B hydrogel nanocomposite, respectively. The adsorption thermodynamic studies suggested that the adsorption process was spontaneous and endothermic for CMC-cl-pAA/Fe3O4-C30B hydrogel nanocomposite. The homogeneous dispersion of the Fe3O4-C30B nanocomposite in the CMC-cl-pAA hydrogel significantly improved the thermal stability, mechanical strength, and excellent regeneration stability. This study demonstrates the application potential of the fascinating properties of CMC-cl-pAA/Fe3O4-C30B hydrogel nanocomposite as a highly efficient adsorbent in the removal of organic dyes from aqueous solution.

Poly(3-aminobenzoic acid) Decorated with Cobalt Zeolitic Benzimidazolate Framework for Electrochemical Production of Clean Hydrogen.

A novel composite of poly(3-aminobenzoic acid) (PABA) and a cobalt zeolitic benzimidazolate framework (CoZIF) has been studied for the production of hydrogen through the hydrogen evolution reaction (HER). The structural characteristics and successful synthesis of PABA, CoZIF and the PABA/CoZIF composite were confirmed and investigated using different techniques. Probing-ray diffraction for phase analysis revealed that the composite showed a decrease and shift in peak intensities, confirming the incorporation of CoZIF on the PABA backbone via in situ polymerization, with an improvement in the crystalline phase of the polymer. The thermal stability of PABA was enhanced upon composite formation. Both scanning electron microscopy and transmission electron microscopy showed that the composite had a rough surface, owing to an interaction between the CoZIF and the external surface of the PABA. The electrochemical hydrogen evolution reaction (HER) performance of the synthesized samples was evaluated using cyclic voltammetry and Tafel analysis. The composite possessed a Tafel slope value of 156 mV/dec and an α of 0.38, suggesting that the Volmer reaction coupled with either the Heyrovsky or Tafel reaction as the rate determining step. The fabricated composite showed high thermal stability and excellent tolerance as well as high electroactivity towards the HER, showing it to be a promising non-noble electrocatalyst to replace Pt-based catalysts for hydrogen generation.

Sequestration of methylene blue dye using sodium alginate poly(acrylic acid)@ZnO hydrogel nanocomposite: Kinetic, Isotherm, and Thermodynamic Investigations.

In this study, a sodium alginate poly(acrylic acid) (SA-poly(AA)) hydrogel and sodium alginate poly(acrylic acid)/zinc oxide (SA-poly(AA)/ZnO) hydrogel nanocomposite (HNC) was synthesized by in situ free-radical polymerization for the sequestration of toxic methylene blue (MB) dye from aqueous solution. The structural properties were analyzed using FTIR, XRD, SEM, TEM, TGA, and DMA The swelling analysis revealed that SA-poly(AA)/ZnO HNC exhibited high water uptake capacity. The kinetics, isotherms, and thermodynamics of adsorption were examined, and results showed that equilibrium data fitted the Langmuir isotherm model, and the adsorption kinetics of MB followed pseudo-second-order model. The maximum adsorption capacity was found to be 1129 mg/g for the SA-poly(AA) hydrogel and 1529.6 mg/g for the SA-poly(AA)/ZnO HNC in 0.25 g/L MB solution at pH 6.0 within 40 min. Thermodynamic parameters for SA-poly(AA) hydrogel and SA-poly(AA)/ZnO HNC substantiated the exothermic and endothermic nature of the adsorption processes, respectively. Moreover, SA-poly(AA)/ZnO HNC presented outstanding reusability with relatively better adsorption efficiencies as compared to SA-poly(AA) hydrogel.

Influence of Magnetic Nanoparticles on Modified Polypyrrole/m-Phenylediamine for Adsorption of Cr(VI) from Aqueous Solution.

A novel, modified polypyrrole/m-phenylediamine (PPy-mPD) composite, decorated with magnetite (Fe3O4) nanoparticles, and prepared via an in-situ oxidative polymerisation, was investigated. The PPy-mPD/Fe3O4 nanocomposite was employed for the removal of highly toxic oxyanion hexavalent chromium Cr(VI) from an aqueous solution. The structure and successful formation of the PPy-mPD/Fe3O4 nanocomposite was confirmed and investigated using various techniques. The presence of Fe3O4 was confirmed by high resolution transmission electron microscopy, with an appearance of Fe lattice fringes. The estimation of the saturation magnetisation of the nanocomposite, using a vibrating sample magnetometer, was observed to be 6.6 emu/g. In batch adsorption experiments, PPy-mPD/Fe3O4 nanocomposite (25 mg) was able to remove 99.6% of 100 mg/L of Cr(VI) at pH 2 and 25 °C. Adsorption isotherms were investigated at different Cr(VI) concentration (100-600 mg/L) and temperature (15-45 °C). It was deduced that adsorption follows the Langmuir model, with a maximum adsorption capacity of 555.6 mg/g for Cr(VI) removal. Furthermore, isotherm data were used to calculate thermodynamic values for Gibbs free energy, enthalpy change and entropy change, which indicated that Cr(VI) adsorption was spontaneous and endothermic in nature. Adsorption-desorption experiments revealed that the nanocomposite was usable for two consecutive cycles with no significant loss of adsorption capacity. This research demonstrates the application potential for the fascinating properties of PPy-mPD/Fe3O4 nanocomposite as a highly efficient adsorbent for the removal of heavy metal ions from industrial wastewater.