Validation of the efficiency of arsenic mitigation strategies in southwestern region of Bangladesh and development of a cost-effective adsorbent to mitigate arsenic levels.

World's highest arsenic (As) contamination is well-documented for the groundwater system of southwestern region (mainly Jashore district) of Bangladesh, where the majority of inhabitants are underprivileged. To mitigate As poisoning in southwestern Bangladesh, numerous steps have been taken so far by the government and non-governmental organizations (NGOs). Among them, digging deep tube wells and As removal by naturally deposited Fe(OH)3 species are being widely practiced in the contaminated areas. However, these actions have been left unmonitored for decades, making people unaware of this naturally occurring deadly poison in their drinking water. Hence, water samples (n = 63, both treated and untreated) and soil samples (n = 4) were collected from different spots in Jashore district to assess the safety level of drinking water and to understand the probable reasons for high As(III) contamination. About 93.7% of samples were found to contain As(III) above 10 µg/L; among them, 38% contained above 50 µg/L. The study shows that current As(III) removal strategies in the study area are ineffective. In this connection, a simple low-cost As(III) removal adsorbent is proposed that can be prepared with very cheap and locally available materials like iron sludge and charcoal. The adsorbent was characterized in terms of SEM, EDX, and XPS. The optimal dosage of the adsorbent was investigated for real-life application concerning several vital water quality parameters. The Fe-C adsorbent exhibited a maximum As(III) removal efficiency of 92% in real groundwater samples. The study will allow policymakers for informed decision-making regarding water body management as well as enable the local people to avail As-safe water in a way that aligns with their economic factors.

Psidium guajava leaf extract mediated green synthesis of silver nanoparticles and its application in antibacterial coatings.

In this study, Psidium guajava (P. guajava) leaf extract-assisted silver nanoparticles (AgNPs) were synthesized and their antibacterial activities were investigated. The synthesized green AgNPs were characterized by various analytical techniques including UV-Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD), field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDX) spectroscopy, etc. From the UV-Vis spectroscopic analysis, the formation of nanoparticles has been confirmed by the color change from light yellow to reddish brown of the solution due to the excitation of the surface plasmon resonance peak at 430 nm. In addition, the FTIR study showed the reduction of Ag ions owing to the presence of biomolecules in the leaf extract, which acted as reducing as well as capping agents. Furthermore, XRD analysis reveals the identified 2θ peaks of AgNPs at ∼39° with cubic structure. The FE-SEM micrograph illustrated the material was formed in nano-dimensions, with an average particle size of ∼12 nm and almost spherical in shape. Moreover, P. guajava-mediated AgNPs demonstrated good antibacterial activity against both Gram-positive (S. aureus) and Gram-negative (E. coli) bacterial strains. The synthesis was performed by a bio-reduction process where a bioactive agent is responsible for reducing metallic ions to metallic nanoparticles as an eco-friendly, cost-effective, non-toxic, one-step, and sustainable method. Therefore, this study may create an imperative synthetic route for the fabrication of green-AgNPs and their application in antibacterial coatings in cotton textiles.

Influence of Y3+ and La3+ ions on the structural, magnetic, electrical, and optical properties of cobalt ferrite nanoparticles.

In the current study, nanocrystalline CoY0.5xLa0.5xFe2-xO4 (where x = 0.00, 0.02, 0.04, 0.06, 0.08, and 0.10) ferrites have been synthesized via a sol-gel auto combustion process. The synthesized powders were pressed into pellet forms and sintered at 900 °C for 4 h in the air. X-ray diffractometry (XRD) confirmed the single-phase cubic spinel structure of the synthesized samples having the mean crystallite domain sizes ranging from 122 and 54 nm. FTIR spectroscopic analyses revealed two strong bands within the range of 600 to 350 cm-1, further confirming the cubic inverse spinel structure of the prepared materials. The surface morphologies and composition were investigated by Field Emission Scanning Electron Microscopy (FE-SEM) and Energy Dispersive X-ray (EDX) Spectroscopy. The magnetic hysteresis curves recorded at room temperature exhibit ferrimagnetic behavior. The highest coercivity (Hc∼1276 Oe) was found at a high doping (x = 0.10) concentration of Y3+ and La3+ in cobalt ferrite. Dielectric constant increase with increased doping concentration whereas real-impedance and dielectric loss decrease with increased in doping concentration and applied frequency. The band gap energy increased from 1.48 to 1.53 eV with increasing Y3+ and La3+concentrations in the UV-Vis region. The elevated levels of magnetic and dielectric substances in the ferrite nanoparticles suggest that the material could be used for magnetic recording media and high-frequency devices.

Phytochemical-Assisted Synthesis of Fe3O4 Nanoparticles and Evaluation of Their Catalytic Activity.

In this study, magnetite nanoparticles (Fe3O4 NPs) were synthesized using Baccaurea ramiflora leaf extracts and characterized by visual observation, UV-Vis, FTIR, XRD, FESEM, and EDS. The UV-Vis spectrum showed continuous absorption at 300-500 nm, confirming the formation of Fe3O4 NPs. FTIR revealed that compounds containing the O-H group act as reducing agents during Fe3O4 NPs formation. Agglomerated spherical NPs were observed in the FESEM image. The prominent peak at ~6.4 keV in the EDS spectrum ascertained the existence of Fe, while the sharp peak at ~0.53 keV confirmed the presence of elemental oxygen. XRD patterns affirmed the crystalline nature. The size of as-synthesized NPs was observed to be 8.83 nm. The catalytic activity of Fe3O4 NPs for the reduction of methylene blue (MB) dye was monitored by UV-Vis. The maximum absorption peak of MB dye at 664 nm was almost diminished within 20 min, which revealed Fe3O4 NPs could be an excellent catalyst for wastewater treatment.

Effects of yttrium doping on structural, electrical and optical properties of barium titanate ceramics.

In this report, we study the Yttrium-doped Barium Titanate (Y-BT) Ba1 - xYxTiO3 (with x = 0.00, 0.01, 0.03, 0.05, 0.07 mmol) perovskite ceramics synthesized by sol-gel method. The as-made powder samples were pressed into a pellet shape and subsequently sintered at 1300 °C for 5 h in air. The structural, morphological, electrical, and optical properties of the synthesized samples were investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), impedance analyzer, and UV-Vis-NIR Spectroscopy respectively. The XRD study revealed the formations of single phase tetragonal structure of Barium Titanate (BT) with ∼23-33 nm mean crystallite size. The crystallite size increases initially with Y-doping, found at about 33 nm for x = 0.01, and reduces for increase in Y3+ concentration further. The microstructural study from FESEM depicts the uniform distribution of compact and well-faceted grain growth for Y-BT in contrast with undoped barium titanate. The average grain size (∼0.29-0.78 µm) of the Y-BT decreases with increasing doping concentration. Frequency-dependent impedance analyses show enhanced dielectric properties like dielectric constant, quality factor, and conductivity with low dielectric loss in the presence of Yttrium. The optical bandgap energy (∼2.63-3.72 eV) estimated from UV-Vis-NIR diffuse reflection data shows an increasing trend with a higher concentration of yttrium doping.