Reports about presence and toxicity of Cd²⁺ in different chemical industrial effluents prompted the researchers to explore some economical, rapid, sensitive, and accurate methods for its determination and removal from aqueous systems. In continuation of series of investigations, adsorption of Cd²⁺ onto the stem of Saccharum arundinaceum is proposed in the present work. Optimization of parameters affecting sorption potential of Cd²⁺ including pH, contact time, temperature, sorbent dose, and concentration of sorbate was carried out to determine best suited conditions for maximum removal of sorbate. To understand the nature of sorption process, linear and nonlinear forms of five sorption isotherms including Freundlich and Langmuir models were employed. Feasibility and viability of sorption process were evaluated by calculating kinetics and thermodynamics of the process, while error analysis suggested best fitted sorption model on sorption data. Thermodynamic studies demonstrated exothermic nature of reaction, while kinetic studies suggested pseudo-second order of reaction.

Herein, we have presented a unique strategy for aqueous synthesis of semiconductor CuInS2 QDs which showed multiple fluorescence. These synthesized CuInS2 QDs were prepared in aqueous media with biocompatible glutathione (GSH), as capping ligand and stabilizer, while the fluorescence and crystallinity were controlled by varying the reaction time. The investigation of various other experimental parameters including precursor’s concentration, effect of pH, and stability of QDs has also been carried out. These QDs were characterized by XRD, TEM, and FT-IR. Meanwhile, optical properties of as synthesized QDs were also investigated by fluorescence spectroscopy. Furthermore, the synthesized QDs were also less cytotoxic and maintained remarkable cell viability up to 100μg/mL. When bioconjugated with Arginyl-glycyl-aspartic acid (RGD) moiety, the obtained CuInS2-RGD QDs have shown higher biocompatibility and good bioimaging performance

Biochar derived from plant biomass has great potential for the decontamination of aqueous media. It is the need of the hour to test biochar derived from economical, easily available, and novel materials. In this regard, the present study provides insight into the sorption of two heavy metals, i.e., cadmium (Cd) and nickel (Ni), using native Arachis hypogaea and its biochar prepared through pyrolysis. The effect of different factors, including interaction time, initial concentration of adsorbate, and temperature, as well as sorbent dosage, was studied on the sorption of Cd and Ni through a batch experiment. Characterization of the native biowaste and prepared biochar for its surface morphology and functional group identification was executed using Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). Results revealed the presence of different functional groups such as -OH on the surface of the adsorbent, which plays an important role in metal attachment. SEM reveals the irregular surface morphology of the adsorbent, which makes it easy for metal attachment. Thermogravimetric analysis shows the stability of A. hypogaea biochar up to 380 °C as compared with native adsorbent. The adsorption efficacy of A. hypogaea was found to be higher than that of native A. hypogaea for both metals. The best adsorption of Cd (94.5%) on biochar was observed at a concentration of 40 ppm, an adsorbent dosage of 2 g, a contact time of 100 min, and a temperature of 50 °C. While the optimum conditions for adsorption of Ni on biochar (97.2% adsorption) were reported at a contact time of 100 min, adsorbent dosage of 2.5 g, initial concentration of 60 ppm, and temperature of 50 °C. Results revealed that biochar offers better adsorption of metal ions as compared with raw samples at low concentrations. Isothermal studies show the adsorption mechanism as physical adsorption, and the negative value of Gibb's free energy confirms the spontaneous nature of the adsorption reaction. An increase in entropy value favors the adsorption process. Results revealed that the sorbent was a decent alternative to eliminate metal ions from the solution instead of costly adsorbents.

Green synthesis is one of the promising pathways for biologically active nanoscale materials. Herein, an eco-friendly synthesis of silver nanoparticles (SNPs) was carried out using an extract of Teucrium stocksianum. The biological reduction and size of NPS were optimized by controlling the physicochemical parameters such as concentration, temperature, and pH. A comparison of fresh and air-dried plant extracts was also undertaken to establish a reproducible methodology. The biosynthesized SNPs were characterized by UV–Vis spectroscopy, FT-IR, SEM, DLS, and XRD analyses. The prepared SNPs exhibited significant biological potential against multi-drug-resistant pathogenic strains. The results revealed that the biosynthesized SNPs exhibit high antimicrobial activity at low concentrations compared to the parent plant extract. Minimum inhibition concentration (MIC) values were found between 5.3 µg/mL to 9.7 µg/mL for the biosynthesized SNPs, whereas the aqueous extract of the plant showed many high values of MIC, i.e., between 69 and 98 µg/ML. Furthermore, the synthesized SNPs were found efficient in the photolytic degradation of methylene blue under sunlight.

Green processes for synthesizing nanocomposites are a hot area of research today as traditional processes are expensive, inefficient, harmful for synthesizing organic and inorganic molecules, and unsuitable for large-scale operations. The present study investigates the capacity of green synthesized Calcium oxide nanoparticles (CaO NPs) for efficiently removing Rhodamine B. Chemical reduction was replaced with Mulberry (Morus nigera) leaf extract as an environmentally friendly reaction mechanism. CaO NPs are characterized by various analytical techniques including EDX, BET, SEM, FTIR, TGA, Zeta Potential, Point of Zero Charge (PZC), and XRD. Maximum adsorption of Rhodamine B by CaO NPs is revealed at an initial concentration of Rhodamine B of 80 ppm, a temperature of 343 K, and contact time of 60 min, 0.4 g of adsorbent at a pH value of 7. Maximum removal of Rhodamine B by CaO NPs was found to be 98.2% which is promising with this small amount of adsorbent (0.4 g). Diverse Kinetic and adsorption isotherms are employed in this study to determine the requirement and significance of the adsorption process. Various adsorption isotherms such as Freundlich, Temkin, Dubinin–Radushkevich (D–R), and Langmuir models have been employed. Among the kinetic adsorption isotherms Elovich, Intraparticle kinetic model, pseudo 1st order, and pseudo 2nd order models were applied. The current study investigates the thorough understanding of the Rhodamine B adsorption process including the mechanism of adsorption using condition optimization, characterization, and model applications. The proposed adsorbent can be employed for the green removal of Rhodamine B from wastewater of industry with maximum efficiency and favorable regeneration properties.

This study reports for the first time the adsorption capacity of a novel adsorbent Croton bonplandianus Baill. biochar. Its adsorption capacity was further enhanced by loading magnetic composites on it, which makes it an efficient medium for the adsorption of dyes. Two azo dyes, Basic Brown 1 (BB₁) and Basic Orange 2 (BO₂), were studied for their effective adsorption from aqueous media. A comprehensive characterization was performed by using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) to study the properties of Fe₂O₃-loaded C. bonplandianus Baill. biochar (FO-CBPBB). A series of batch experiments were conducted to optimize various parameters (pH, contact time, adsorbent amount, initial BB₁ and BO₂ concentrations, and temperature) for the maximum adsorption of BB₁ and BO₂ on the FO-CBPBB adsorbent. The percentage of BB₁ and BO₂ dyes that adsorb to FO-CBPBB under the best experimental circumstances (pH of solution 7, contact time 80 min, temperature of solution 40 °C, initial BB₁ and BO₂ dye concentrations 80 mg L^-1, and adsorbent dose 1 g L^-1) was 93 and 95%, respectively. The best adsorption of BB₁ and BO₂ was accomplished by optimizing the effects of several factors, including the starting dye concentration, contact time, and temperature, based on the central composite design. The Freundlich and Langmuir isotherm models were used to examine the equilibrium data. The Langmuir isotherm with the greatest adsorption capacity and R² value effectively captured the experimental results. When kinetic parameters were investigated, it was found that pseudo-second-order was appropriate, reflecting the fact that the dye-adsorbent interaction was the rate-controlling factor in this study. The sorption process was endothermic and spontaneous, as shown by the thermodynamic variables. Based on the interaction between the adsorbent and azo dyes, it was concluded that the adsorption process was electrostatic in nature. Adsorbents that have been synthesized can effectively remove azo dyes from wastewater. Excellent regeneration efficiency was exhibited by FO-CBPBB, which makes it an eco-friendly and cost-effective alternative to other costly techniques applied for water purification.