In this study, polypyrrole-based activated carbon was prepared by the carbonization of polypyrrole at 650 °C for 2 h in the presence of four-times the mass of KOH as a chemical activator. The structural and morphological properties of the product (polypyrrole-based activated carbon (PPyAC4)), analyzed by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and thermogravimetric analysis, support its applicability as an adsorbent. The adsorption characteristics of PPyAC4 were examined through the adsorption of lead ions from aqueous solutions. The influence of various factors, including initial ion concentration, pH, contact time, and adsorbent dose, on the adsorption of Pb²⁺ was investigated to identify the optimum adsorption conditions. The experimental data fit well to the pseudo-second-order kinetic model (R² = 0.9997) and the Freundlich isotherm equation (R² = 0.9950), suggesting a chemisorption pathway. The adsorption capacity was found to increase with increases in time and initial concentration, while it decreased with an increase in adsorbent dose. Additionally, the highest adsorption was attained at pH 5.5. The calculated maximum capacity, q_m, determined from the Langmuir model was 50 mg/g.

In this study, we report the fabrication of graphitic carbon nitride doped zinc oxide nanocomposites, g-C₃N₄/ZnO, (Zn-Us) by using different amount of urea. They were further characterized by X-ray Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Raman, UV-vis, Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM) techniques. The prepared nanocomposites were used as photocatalysts for the mineralization of the light sensitive dyes Methylene Blue (MB) and Rose Bengal (RB) under UV light irradiation, and corresponding photo-mechanism was proposed. Benefiting from these photocatalytic characteristics, urea derived g-C₃N₄/ZnO photocatalysts have been found to have excellent photodegradation activity against the MB and RB for 6 h and 4 h, respectively. Under the given experimental conditions, the degradation percentage of fabricated Zn-Us were shown ~90% for both model dyes. Compared to cationic MB dye, anionic RB dye is more actively degraded on the surface of prepared photocatalysts. The results obtained can be effectively used for future practical applications in wastewater treatment

The adsorption of methyl orange (MO) from aqueous solutions onto a KOH-activated polypyrrole-based adsorbent (PACK) was investigated using batch and fixed-bed column techniques. The structural, thermal, and morphological properties of the PACK, analyzed by various methods, support its applicability as an adsorbent. An adsorption kinetic study revealed a preferably pseudo-second-order (R² = 0.9996) and rate-limiting step controlled by both film and intra-particle diffusions. The thermodynamic adsorption tests resulted in negative ΔG°, ΔH°, and ΔS° values, which decreased as the temperature and concentration increased, indicating the spontaneous and exothermic adsorption over 25–45 °C. The adsorption isotherms fit the experimental data in the order of Langmuir ≈ Freundlich > Temkin, with evidence of adsorption operating well via the monolayer physical adsorption process, and maximum monolayer adsorption ranging from 520.8 to 497.5 mg/g. The breakthrough curve of the fixed-bed column experiment was modeled using the Thomas, Yoon–Nelson, and Hill models, resulting in an equilibrium capacity of 57.21 mg/g. A 73% MO recovery was achieved, indicating the possibility of column regeneration. Compared to other adsorbents reported, PACK had comparable or even superior capacity toward MO. For cost-effectiveness, similar nitrogen-containing polymeric wastes could be exploited to obtain such excellent materials for various applications.

Various ZnO nanomaterials such as nanorods, nanoparticles, and nanosheets were synthesized using Salvadora persica leaf extract via the sol–gel method. The prepared nanomaterials possess a large number of nanocavities. The synthesized nanomaterials were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), UV-visible diffuse reflectance studies (UV-DRS), scanning electron microscopy (SEM), and high resolution transmission electron microscopy (HT-TEM), and these nanomaterials were used to test photocatalytic applications for the degradation of highly hazardous methylene blue dye. The degradation efficiency was higher for materials with nanorods and nanosheets with nanocavities; this was due to the presence of the nanocavities, which made the catalyst more sensitive to light absorption. This method offers a green synthesis of different nanomaterials in bulk quantity at low cost.

The dwindling of global petroleum deposits and worsening environmental issues have triggered researchers to find an alternative energy such as biodiesel. Biodiesel can be produced via transesterification of vegetable oil or animal fat with alcohol in the presence of a catalyst. A heterogeneous catalyst at an economical price has been studied widely for biodiesel production. It was noted that various types of natural waste shell are a potential calcium resource for generation of bio-based CaO, with comparable chemical characteristics, that greatly enhance the transesterification activity. However, CaO catalyzed transesterification is limited in its stability and studies have shown deterioration of catalytic reactivity when the catalyst is reused for several cycles. For this reason, different approaches are reviewed in the present study, which focuses on modification of waste-shell derived CaO based catalyst with the aim of better transesterification reactivity and high reusability of the catalyst for biodiesel production. The catalyst stability and leaching profile of the modified waste shell derived CaO is discussed. In addition, a critical discussion of the structure, composition of the waste shell, mechanism of CaO catalyzed reaction, recent progress in biodiesel reactor systems and challenges in the industrial sector are also included in this review.

The composite of ceria has been widely studied as an electrode material for supercapacitors applications due to its high energy density. Herein, we synthesize CeO₂/NiO nanocomposite via a hydrothermal route and explore its different aspects using various characterization techniques. The crystal structure is investigated using X-ray diffraction, Fourier transform infrared, and Raman spectroscopy. The formation of nanoflakes which combine to form flower-like morphology is observed from scanning electron microscope images. Selected area scans confirm the presence of all elements in accordance with their stoichiometric amount and thus authenticate the elemental purity. Polycrystalline nature with crystallite size 8–10 nm having truncated octahedron shape is confirmed from tunneling electron microscope images. Using X-ray photoelectron spectroscopy the different oxidation states of Ce and Ni are observed which play the role of active sites in the electrochemical performance of this nanocomposite material. Cyclic Voltammetry(CV) measurements at different scan rates and Galvanic Charge Discharge (GCD) measurements at different current densities are performed to probe the electrochemical response which revealed the potential of CeO₂/NiO nanocomposite as an electrode material for energy storage devices.