The catalytic activity of Pd/ZrO₂ was studied in terms of the degradation of rhodamine-B dye in the presence of hydrogen peroxide. Pd/ZrO₂ was prepared by impregnation method, calcined at 750 °C and characterized by XRD, SEM and EDX. The catalyst showed good catalytic activity for dye degradation at 333 K, using 0.05 g of the catalyst during 5 h. The reaction kinetics followed the pseudo-first order kinetics. The Freundlich, Langmuir and Temkin isotherms were applied to the data and the best fit was obtained with Freundlich isotherm. Thermodynamic parameters, like ΔH, ΔG and ΔS were also calculated. The negative values of ΔH (−291.406 KJ/mol) and Gibbs free energy (ΔG) showed the exothermic and spontaneous nature of the process. The positive ΔS (0.04832 KJ/mol K) value showed suitable affinity of catalyst for dye degradation. The catalyst was very stable, active and was easily separated from the reaction mixture by filtration. It can be concluded from the results that the prepared catalyst could be effectively used in dyes degradation/removal from water subjected to further validation and use for various dyes.

The current research focused on the super capacitive behavior of organic conducting polymer, i.e., polypyrrole (PPy) and its composites with gum arabic (GA) prepared via inverse emulsion polymerization. The synthesized composites material was analyzed by different analytical techniques, such as UV-visible, FTIR, TGA, XRD, and SEM. The UV-Vis and FTIR spectroscopy clearly show the successful insertion of GA into PPy matrix. The TGA analysis shows high thermal stability for composites than pure PPy. The XRD and SEM analysis show the crystalline and amorphous structures and overall morphology of the composites is more compact and mesoporous as compared to the pure PPy. The electrochemical properties of modified solid state supercapacitors established on pure polypyrrole (PPy), polypyrrole/gum arabic (PPy/GA) based composites were investigated through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge–discharge (GCD). The specific capacitance of the PPy modified gold electrode is impressive (~168 F/g). The specific capacitance of PPy/GA 1 electrode has been increased to 368 F/g with a high energy density and power density (~73 Wh/kg), and (~599 W/kg) respectively.

Methyl red (MR) dye, one of the azo dyes, is mutagenic and its persistence has negative effects on the environment and people’s health. The current work is the first to demonstrate that methyl red dye can be removed effectively and sustainably, utilizing biomass derived from the bark of the Dodonaea viscosa (Hopbush) plant. The Hopbush bark shows effective adsorption of MR, upto 73%, under optimized conditions in an aqueous medium. The experimental conditions were optimized by examining the effect of time, initial dye concentration, pH and ionic strength on the adsorption process in an aqueous medium. Maximum (i.e., 73%) adsorption of MR removal (500 ppm) was observed in highly acidic conditions (pH = 1) at a contact time of 75 min. The pseudo-second-order kinetic model and Freundlich adsorption isotherm appeared to be the most appropriate for characterizing the MR’s adsorption onto the bark of the D. viscosa plant. Furthermore, it was shown that bark powder outperformed animal charcoal, silica gel, and powdered flowers, as well as the leaves of the same species, in terms of adsorption capacity. Thus, a natural adsorbent that is inexpensive and readily available—the bark of the D. viscosa plant—can be used to effectively remove harmful dyes from contaminated water and protect water resources from harmful pollutants.

The presence of dyes in water stream is a major environmental problem that affects aquatic and human life negatively. Therefore, it is essential to remove dye from wastewater before its discharge into the water bodies. In this study, Banyan (Ficus benghalensis, F. benghalensis) tree leaves, a low-cost biosorbent, were used to remove brilliant green (BG), a cationic dye, from an aqueous solution. Batch model experiments were carried out by varying operational parameters, such as initial concentration of dye solution, contact time, adsorbent dose, and pH of the solution, to obtain optimum conditions for removing BG dye. Under optimum conditions, maximum percent removal of 97.3% and adsorption capacity (Qe) value of 19.5 mg/g were achieved (at pH 8, adsorbent dose 0.05 g, dye concentration 50 ppm, and 60 min contact time). The Langmuir and Freundlich adsorption isotherms were applied to the experimental data. The linear fit value, R² of Freundlich adsorption isotherm, was 0.93, indicating its best fit to our experimental data. A kinetic study was also carried out by implementing the pseudo-first-order and pseudo-second-order kinetic models. The adsorption of BG on the selected biosorbent follows pseudo-second-order kinetics (R² = 0.99), indicating that transfer of internal and external mass co-occurs. This study surfaces the excellent adsorption capacity of Banyan tree leaves to remove cationic BG dye from aqueous solutions, including tap water, river water, and filtered river water. Therefore, the selected biosorbent is a cost-effective and easily accessible approach for removing toxic dyes from industrial effluents and wastewater.

Nile blue (NB) dye is a highly toxic substance that when discharged into sewage presents a significant risk to the environment and human health. Carbon-based nanomaterials, such as graphene oxide (GO), reduced graphene oxide (rGO), and their nanocomposites, offer considerable potential for eliminating hazardous pollutants from aqueous systems. In this study, we have successfully fabricated bare GO and rGO, and then, the rGO was decorated with silver (Ag) nanoparticles to develop the Ag-rGO composite. The as-prepared materials were characterized by various techniques, such as UV-visible (UV-vis) and Fourier transform infrared (FTIR) spectroscopies, X-ray diffraction (XRD), energy-dispersive X-ray (EDX), and scanning electron microscopy (SEM) to elucidate their structure, morphology, and chemical composition. The pollutant removal performance of the as-prepared materials was evaluated through a batch approach under the effect of various experimental variables for removal of NB dye from wastewater. As obvious, the Ag-rGO composite revealed exceptional performance for NB dye removal from wastewater, with a maximum removal percentage of 94% within 60 min, which is remarkably higher than those of the rGO (i.e., 59%) and GO (i.e., 22%), under the same experimental conditions. The adsorption data was analyzed with thermodynamics, isotherms, and kinetics models to better understand the physicochemical mechanisms driving the effective removal of the NB dye. The results reveal that Ag-rGO nanocomposite exhibit excellent adsorption ability as well as favorable thermodynamic and kinetic parameters for NB dye removal. It was also found that the presence of light enhanced the adsorptive removal of NB while using Ag-rGO as an adsorbent. The present study noted significant reusability of the Ag-rGO nanocomposite, likely due to minimal Ag leaching and/or the robust stability of the Ag-rGO. It is suggested that Ag-rGO-based hybrid materials could serve as promising candidates for efficiently adsorbing and catalytically removing various toxic pollutants from wastewater.

Partially biodegradable polymer nanocomposites Poly(3-Hydroxybutyrate) (PHB)/MultiwalledCarbon Nanotubes (MWCNTs)/Poly(Methyl Methacrylate) (PMMA)and non-biodegradable nanocomposites (MWCNTs/PMMA) were synthesized, and their thermal, electrical, and ammonia-sensing properties were compared. MWCNTs were chemically modified to ensure effective dispersion in the polymeric matrix. Pristine MWCNTs (p-MWCNTs) were functionalized with –COOH (a-MWCNTs) and amine groups (f-MWCNTs). Then, PHB grafted multiwalled carbon nanotubes (g-MWNTs) were prepared by a ‘grafting to’ technique. The p-MWCNTs, a-MWCNTs, f-MWCNTs, and g-MWCNTs were incorporated into the PMMA matrix and PMMA/PHB blend system by solution mixing. The PHB/f-MWCNTs/PMMA blend system showed good thermal properties among all synthesized nanocomposites. Results from TGA and dTGA analysis for PHB/f-MWCNTs/PMMA showed delay in T₅ (about 127 °C), T₅₀ (up to 126 °C), and T_max (up to 65 °C) as compared to neat PMMA. Higher values of frequency capacitance were observed in nanocomposites containing f-MWCNTs and g-MWCNTs as compared to nanocomposites containing p-MWCNTs and a-MWCNTs. This may be attributed to their excellent interaction and good dispersion in the polymeric blend. Analysis of ammonia gas-sensing data showed that PHB/g-MWCNTs/PMMA nanocomposites exhibited good sensitivity (≈100%) and excellent repeatability with a constant response. The calculated limit of detection (LOD) is 0.129 ppm for PHB/g-MWCNTs/PMMA, while that of all other nanocomposites is above 40 ppm.