This investigation aimed at evaluating the efficiency of micro and nanoclays as a low-cost material for the removal of crystal violet (CV) dye from an aqueous solution. The impacts of various factors (contact time, pH, adsorbent dosage, temperature, initial dye concentration) on the adsorption process have been taken into consideration. Six micro and nanoclay samples were obtained by treating clay materials collected from different locations in the Albaha region, Saudi Arabia. Out of the six tested micro and nanoclays materials, two (NCQ1 and NCQ3) were selected based on the highest adsorption efficiency for complete experimentation. The morphology and structure of the selected micro and nanoclay adsorbents were characterized by various techniques: SEM-EDX, FTIR, XRF, XRD, and ICP-MS. The XRF showed that the main oxides of both nanoclays were SiO₂, Al₂O₃, Fe₂O₃, K₂O, CaO, and MgO, and the rest were impurities. All the parameters affecting the adsorption of CV dye were optimized in a batch system, and the optimized working conditions were an equilibrium time of 120 min, a dose of 30 mg, a temperature of 25 °C, and an initial CV concentration of 400 mg/L. The equilibrium data were tested using nonlinear isotherm and kinetic models, which showed that the Freundlich isotherm and pseudo-second-order kinetics gave the best fit with the experimental data, indicating a physico-chemical interaction occurred between the CV dye and both selected micro and nanoclay surfaces. The maximum adsorption capacities of NCQ1 and NCQ3 adsorbents were 206.73 and 203.66 mg/g, respectively, at 25 °C. The thermodynamic factors revealed that the CV dye adsorption of both micro and nanoclays was spontaneous and showed an exothermic process. Therefore, the examined natural micro and nanoclays adsorbents are promising effective adsorbents for the elimination of CV dye from an aqueous environment.

The current research intended to employ a facile and economical process, which is also ecofriendly to transform camel waste bones into novel heterostructure for cleansing of diverse waste waters. The bones of camel were utilized for preparation of hydroxyapatite by hydrothermal method. The prepared hydroxyapatite was applied to the synthesis of cerium oxide-hydroxyapatite coated with natural polymer chitosan (CS-HAP-CeO₂) heterostructure. Being abundant natural polymer polysaccharide, chitosan possesses exceptional assets such as accessibility, economic price, hydrophilicity, biocompatibility as well as biodegradability, therefore style it as an outstanding adsorbent for removing colorant and other waste molecules form water. This heterostructure was characterized by various physicochemical processes such as XRD, SEM-EDX, TEM, and FT-IR. The CS-HAP-CeO₂ was screened for adsorption of various industrially important dyes, viz., Brilliant blue (BB), Congo red (CR), Crystal violet (CV), Methylene blue (MB), Methyl orange (MO), and Rhodamine B (RB) which are collective pollutants of industrial waste waters. The CS-HAP-CeO₂ demonstrated exceptional adsorption against CR dye. The adsorption/or removal efficiency ranges are BB (11.22%), CR (96%), CV (28.22%), MB (47.74%), MO (2.43%), and RB (58.89%) dyes. Moreover, this heterostructure showed excellent bacteriostatic potential for E. coli, that is liable for serious waterborne diseases. Interestingly, this work revealed that the incorporation of cerium oxide and chitosan into hydroxyapatite substantially strengthened antimicrobial and adsorption capabilities than those observed in virgin hydroxyapatite. Herein, we recycled the unwanted camel bones into a novel heterostructure, which assists to reduce water pollution, mainly caused by the dye industries.

In this work, magnetized activated Juniperus procera leaves (Fe₃O₄@AJPL) were successfully prepared via chemical activation of JPL and in situ coprecipitation with Fe₃O₄. A Fe₃O₄@AJPL nanocomposite was successfully applied for the elimination of malachite green (MG) dye from aqueous media. The prepared Fe₃O₄@AJPL adsorbent was characterized by SEM, EDX, TEM, XRD, FTIR, TGA, and BET surface area analyses. The BET surface area and pore size of the Fe₃O₄@AJPL nanocomposite were found to be 38.44 m²/g and 10.6 nm, respectively. The XRD and FTIR results indicated the formation of a Fe₃O₄@AJPL nanocomposite. Different parameters, such as pH of the solution (3–8), adsorbent dosage (10–100 mg), temperature (25–45°C), contact time (5-240 min), and initial MG concentrations (20–350 mg/L), for the elimination of the MG dye using Fe₃O₄@AJPL were optimized and found to be 7, 50 mg, 45°C, 120 min, and 150 mg/L, respectively. The nonlinear isotherm and kinetic studies exhibited a better fitting to second-order kinetic and Langmuir isotherm models, with a maximum monolayer adsorption capacity of 318.3 mg/g at 45°C, which was highly superior to the previously reported magnetic nanocomposite adsorbents. EDX analyses confirmed the presence of nitrogen on the Fe₃O₄@AJPL surface after MG adsorption. The calculated thermodynamic factors indicated endothermic and spontaneous processes. The desorption of MG dye from Fe₃O₄@AJPL was performed using a solution of 90% ethanol. Finally, it could be concluded that the designed Fe₃O₄@AJPL magnetic nanocomposite will be a cost-effective and promising adsorbent for the elimination of MG from aqueous media.

Environmental pollution, especially water pollution caused by dyes, heavy metal ions and biological pathogens, is a root cause of various lethal diseases in human-beings and animals. Water purification materials and treatment methods are overpriced. Consequently, there is an imperative outlook observance for cheap materials for the purification of wastewaters. In order to fill up the projected demand for clean water, the present study aimed to make use of cost-effective and environmentally friendly methods to convert bone-waste from animals such as cows into novel composites for the decontamination of water. The bone-waste of slaughtered cows from the Najran region of Saudi Arabia was collected and used for the synthesis of hydroxyapatite based on the thermal method. The synthesized hydroxyapatite (Ca₁₀(PO₄)₆(OH)₂) was utilized to prepare a manganese ferrite/hydroxyapatite composite. The nanocomposite was categorized by diverse sophisticated procedures, for instance XRD, FE-SEM, EDX, TEM, UV, PL and FT-IR. This composite possesses outstanding photocatalytic activity against methylene blue dye, which is a common pollutant from industrial wastes. Moreover, the synthesised composite revealed exceptional bacteriostatic commotion towards E. coli and S. aureus bacteria, which are accountable for acute waterborne infections. The outcome of this study demonstrated that the integration of manganese ferrite into hydroxyapatite significantly intensified both antimicrobial and photocatalytic actions when compared to the virgin hydroxyapatite.

In this study, activated residual Dodonaea Viscosa (ARDV) was synthesized by the simple chemical activation process as a cost-effective and sustainable adsorbent for the efficient elimination of methyl green molecule (MG) from water. The prepared ARDV was characterized by TGA, SEM, EDX, FTIR, and BET surface area analysis. The adsorption properties and mechanisms toward MG were examined using the batch method. The optimal conditions for adsorption of Pb(II) were pH= 6.6, [ARDV] =0.1 g, time=180 min, and temperature= 65°C. The adsorption isotherms and kinetics study was conducted and the resulting data fitted well with Langmuir and PSO model. The maximum sorption capacity of 99 mg/g was obtained from Langmuir isotherm for MG at 60 °C. According to thermodynamic parameters, the adsorption of MG on ARDV was endothermic and spontaneous. Hence, it could be concluded that ARDV is an inexpensive and effective bio-adsorbent for the removal of MG from polluted water.