This report deals with converting the agriculture waste (rice straw) to environmental cleaner materials (biochar) using airless pyrolysis followed by eco-friendly activation. The biochar (p-Biochar) obtained after pyrolysis step (poorly active material) was activated using wet attrition method to give m-Biochar (highly active materials). The both p-Biochar and m-Biochar were characterized in detail and utilized for MB and CV dye removal from aqueous solution. Various parameters affecting the adsorption process such as dye concentration, adsorbent dose, contact time, temperature, NaCl dose and pH were investigated. The adsorption isotherm was well fitted using Langmuir isotherm, and the maximum adsorption capacity is 90.91 and 44.64 mg/g, for MB and CV dyes, respectively. The contact time data obtained showed that the two dyes were poorly adsorbed over p-Biochar. The equilibrium was reached quickly in 15 min for MB dye and 20 min for CV dye using the m-Biochar, and removal percent was 94.45 and 92.70% for MB and CV dyes, respectively. Moreover, the kinetic isotherm presented very well fitted by pseudo-second-order model. In addition, the adsorption percent increases with further increasing the pH value. Finally, we observed that m-Biochar highly adsorbs the MB dye compared with the CV dye over all experimental conditions.

Recently, nanofibers have come to be considered one of the sustainable routes with enormous applicability in different fields, such as wastewater treatment. Electrospun nanofibers can be fabricated from various materials, such as synthetic and natural polymers, and contribute to the synthesis of novel nanomaterials and nanocomposites. Therefore, they have promising properties, such as an interconnected porous structure, light weight, high porosity, and large surface area, and are easily modified with other polymeric materials or nanomaterials to enhance their suitability for specific applications. As such, this review surveys recent progress made in the use of electrospun nanofibers to purify polluted water, wherein the distinctive characteristics of this type of nanofiber are essential when using them to remove organic and inorganic pollutants from wastewater, as well as for oil/water (O/W) separation.

The main aim of this work is to treat sugarcane bagasse agricultural waste and prepare an efficient, promising, and eco-friendly adsorbent material. Biochar is an example of such a material, and it is an extremely versatile and eco-friendly biosorbent to treat wastewater. Crystal violet (CV)-dye and methylene blue (MB)-dye species are examples of serious organic pollutants. Herein, biochar was prepared firstly from sugarcane bagasse (SCB), and then a biochar biosorbent was synthesized through pyrolysis and surface activation with NaOH. SEM, TEM, FTIR, Raman, surface area, XRD, and EDX were used to characterize the investigated materials. The reuse of such waste materials is considered eco-friendly in nature. After that, the adsorption of MB and CV-species from synthetically prepared wastewater using treated biochar was investigated under various conditions. To demonstrate the study’s effectiveness, it was attempted to achieve optimum effectiveness at an optimum level by working with time, adsorbent dose, dye concentration, NaCl, pH, and temperature. The number of adsorbed dyes reduced as the dye concentrations increased and marginally decreased with NaCl but increased with the adsorbent dosage, pH, and temperature of the solution increased. Furthermore, it climbed for around 15 min before reaching equilibrium, indicating that all pores were almost full. Under the optimum condition, the removal perecentages of both MB and CV-dyes were ≥98%. The obtained equilibrium data was represented by Langmuir and Freundlich isotherm models. Additionally, the thermodynamic parameters were examined at various temperatures. The results illustrated that the Langmuir isotherm was utilized to explain the experimental adsorption processes with maximum adsorption capacities of MB and CV-dyes were 114.42 and 99.50 mgg⁻¹, respectively. The kinetic data were estimated by pseudo-first and pseudo-second-order equations. The best correlation coefficients of the investigated adsorption processes were described by the pseudo-second-order kinetic model. Finally, the data obtained were compared with some works published during the last four years.

In this study, the preparation of graphene oxide@chitosan (GO@CS) composite beads was investigated via continuous dropping techniques to remove methylene blue (MB)-dye from an aqueous media. The prepared beads were characterized using various techniques before and after the adsorption of MB. The experimental results showed that the adsorption processes fit the kinetic pseudo-second-order and Langmuir isotherm models. Moreover, the GO@CS beads achieve maximum adsorption capacities of 23.26 mg g⁻¹, which was comparable with other adsorbents in the literature. An important advantage of our adsorbent is that the GO@CS can remove 82.1% of the real sample color within 135 min.

This work addresses a simple method to functionalize graphene oxide with sodium carboxymethyl cellulose using tetraethyl orthosilicate as a linker for rapid and significant removal of Nd(III) and Ce(III) from aqueous solutions. The prepared composite (GO–CMC) was characterized by different techniques to confirm the modification and adsorption process. The sorption performance of the GO–CMC was evaluated using Nd(III) and Ce(III) as absorbent materials. The experimental results demonstrated that the sorption process was excellently fitted by the pseudo-second-order kinetic model. The adsorption results were also analyzed by different isotherm models. According to the Langmuir isotherm model, the experimental sorption capacities at pH 3.0 was 661.21 and 436.55 mg/g for Nd(III) and Ce(III), respectively. The thermodynamic results indicated that the sorption process of the two examined metal ions was endothermic and spontaneous. The regenerated GO–CMC composite has a similar removal percentage to the original composite. These results confirmed that the prepared composite (GO–CMC) could be used as an effective adsorbent for Nd(III) and Ce(III) from certain multielement solutions.

In this review, we focus on some interesting and recent examples of various applications of organic azides such as their intermolecular or intramolecular, under thermal, catalyzed, or noncatalyzed reaction conditions. The aforementioned reactions in the aim to prepare basic five-, six-, organometallic heterocyclic-membered systems and/or their fused analogs. This review article also provides a report on the developed methods describing the synthesis of various heterocycles from organic azides, especially those reported in recent papers (till 2020). At the outset, this review groups the synthetic methods of organic azides into different categories. Secondly, the review deals with the functionality of the azido group in chemical reactions. This is followed by a major section on the following: (1) the synthetic tools of various heterocycles from the corresponding organic azides by one-pot domino reaction; (2) the utility of the chosen catalysts in the chemoselectivity favoring C−H and C-N bonds; (3) one-pot procedures (i.e., Ugi four-component reaction); (4) nucleophilic addition, such as Aza-Michael addition; (5) cycloaddition reactions, such as [3+2] cycloaddition; (6) mixed addition/cyclization/oxygen; and (7) insertion reaction of C-H amination. The review also includes the synthetic procedures of fused heterocycles, such as quinazoline derivatives and organometal heterocycles (i.e., phosphorus-, boron- and aluminum-containing heterocycles). Due to many references that have dealt with the reactions of azides in heterocyclic synthesis (currently more than 32,000), we selected according to generality and timeliness. This is considered a recent review that focuses on selected interesting examples of various heterocycles from the mechanistic aspects of organic azides.