Ijraset Journal For Research in Applied Science and Engineering Technology
Authors: Prashant P. Mungle, Priyadarshani N. Deshmukh, Pravin K. Gaidhane
DOI Link: https://doi.org/10.22214/ijraset.2026.78100
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The investigation of instantaneous removal of multiple organic pollutants from using nanomaterials flags an innovative opportunity that is permitted from subordinate pollution and economical. In the aquatic atmosphere, river water contains large amount of organic effluent releases from the textile industries, which can stimulus the process of adsorption hence, the removal of toxic organic pollutant from the water bodies becomes a true challenge. Owing to this, we try to synthesize of Bi2MoO6 NPs using Euphorbia leaf extracts as green reducing and capping agents, leaf extracts play a dual role to reduce both bismuth and molybdenum into corresponding metal oxide. As synthesized material were characterized various spectroscopic and microscopic techniques for the structural and morphological authentication. X-ray diffraction (XRD) confirmed the orthorhombic phase with crystalline size 10-12 nm. Elemental composition and purity of the NPs (Bi, Mo, C, and O elements) were confirmed via energy-dispersive X-ray spectroscopy (EDS). UV-DRS exposes band gap about 2.44 eV, which exhibited excellent semiconducting property for the removal of toxic compound. Surface area and pore size were assessed by Brunauer–Emmett–Teller (BET) analysis, obtained surface area found to be 82. 66 m2/g and pore size was 9.9 nm. Morphological studies and particle size distribution were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), TEM revealed nearly spherical NPs with average particle size 30-35 nm. However, the adsorption studies revealed that Bi2MoO6 NPs exhibit an outstanding removal e?ciency for different dyes found to be 60.3, 79.5 and 66.8 mg g?¹ for Erichrome black T (EBT), Malachite green (MG) and Eosin yellow (EY) respectively. However, the kinetic studies follows pseudo-second order kinetics, and the equilibrium data authenticate for Freundlich and Langmuir isotherm. Furthermore, Bi2MoO6 NPs showed excellent activity against E. coli, S. aureus followed by B. subtilis and K. pneumoniae. DPPH scavenging activity, in methanolic solvent showed higher radical inhibition than ethanolic solvent.
This study addresses the growing problem of water pollution, particularly contamination caused by industrial organic dyes, heavy metals, pesticides, and pharmaceutical residues. Traditional wastewater treatment methods such as adsorption, coagulation, and photodegradation are commonly used, but they face limitations. Although nanomaterials offer high efficiency, many are difficult to separate, recover, and may pose environmental risks.
To overcome these challenges, the study develops a green synthesis approach for preparing bismuth molybdate (Bi?MoO?) nanoparticles using Euphorbia leaf extract as a natural reducing and stabilizing agent. This eco-friendly method avoids toxic chemicals and high energy consumption associated with conventional synthesis techniques. The synthesized nanoparticles were characterized using techniques such as XRD, FTIR, SEM, TEM, EDX, UV–DRS, and BET analysis, confirming their crystalline, nanoscale, and phase-pure structure.
The prepared Bi?MoO? nanoparticles were tested for:
Dye removal (adsorption studies) using EBT, Methylene Green, and Eosin Yellow.
Maximum adsorption capacities were 60.3, 79.5, and 66.8 mg/g, respectively.
Adsorption followed pseudo-second-order kinetics and fit both Langmuir and Freundlich isotherm models.
Antibacterial activity against E. coli, S. aureus, K. pneumoniae, and B. subtilis, showing effective inhibition.
Antioxidant activity using the DPPH assay, with stronger radical scavenging in methanol than ethanol.
Overall, the study demonstrates that plant-mediated green-synthesized Bi?MoO? nanoparticles are effective, eco-friendly materials for wastewater treatment, antimicrobial applications, and antioxidant activity, making them promising for environmental remediation.
In conclusion, the existing work fruitfully exposed the green synthesis of Bi2MoO6 NPs using Euphorbia leaf extract, which performed a dual role as both the reducing and capping agent. As synthesized material were authenticate for their structural and morphological explorations techniques recognised the operative formation of the NPs. The TEM analysis exposed that of Bi2MoO6 NPs having a size of nearly 30-35 nm. The result explored a single-phase orthorhombic phase. Furthermore, the NPs exhibited a large surface area of 82. 66 m2/g, confirming their mesoporous nature. The Bi2MoO6 adsorbent revealed a remarkable removal efficiency for MG, EY and EBT even at small doses, under environmentally conditions. The mechanistic methodology of adsorption kinetically scrutinized the pseudo-second-order kinetic model, while the equilibrium data were fitted for both Langmuir and Freundlich isotherms reinforced the surface interaction mechanisms between the NPs and organic toxic dyes. The maximum removal e?ciency was found to be 60.3, 79.5 and 66.8 mg g?¹ for EBT, MG and EY dyes respectively. Moreover, Bi2MoO6 NPs showed exceptional activity at a concentration of 0.1mg/100µL against E. coli (23 mm), S. aureus (22 mm) followed by K. pneumonia (17 mm) and B. subtilis (13 mm). The DPPH scavenging activity, in methanolic solvent showed higher radical inhibition activity than ethanolic solvent. The compared result with standard ascorbic acid in all concentration of assay, Euphorbia extract, Bi2MoO6 NPs showed maximum inhibition at a concentration of 500 ?g/mL in both solvents. In Complete, synthesized Bi2MoO6 NPs offer an encouraging, workable solution for an effective elimination of toxic heavy metal ions from the aqua sphere as well as good sustainability against microbial pathogens.
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Copyright © 2026 Prashant P. Mungle, Priyadarshani N. Deshmukh, Pravin K. Gaidhane. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Paper Id : IJRASET78100
Publish Date : 2026-03-10
ISSN : 2321-9653
Publisher Name : IJRASET
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