An Eco-Friendly Synthesis Approach for Enhanced Photocatalytic and Antibacterial Properties of Copper Oxide Nanoparticles Using Coelastrella terrestris Algal Extract.

Background: In the current scenario, the synthesis of nanoparticles (NPs) using environmentally benign methods has gained significant attention due to their facile processes, cost-effectiveness, and eco-friendly nature. Methods: In the present study, copper oxide nanoparticles (CuO NPs) were synthesized using aqueous extract of Coelastrella terrestris algae as a reducing, stabilizing, and capping agent. The synthesized CuO NPs were characterized by X-ray diffraction (XRD), UV-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), and field emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray spectroscopy (EDS). Results: XRD investigation revealed that the biosynthesized CuO NPs were nanocrystalline with high-phase purity and size in the range of 4.26 nm to 28.51 nm. FTIR spectra confirmed the existence of secondary metabolites on the surface of the synthesized CuO NPs, with characteristic Cu-O vibrations being identified around 600 cm-1, 496 cm-1, and 440 cm-1. The FE-SEM images predicted that the enhancement of the algal extract amount converted the flattened rice-like structures of CuO NPs into flower petal-like structures. Furthermore, the degradation ability of biosynthesized CuO NPs was investigated against Amido black 10B (AB10B) dye. The results displayed that the optimal degradation efficacy of AB10B dye was 94.19%, obtained at 6 pH, 50 ppm concentration of dye, and 0.05 g dosage of CuO NPs in 90 min with a pseudo-first-order rate constant of 0.0296 min-1. The CuO-1 NPs synthesized through algae exhibited notable antibacterial efficacy against S. aureus with a zone of inhibition (ZOI) of 22 mm and against P. aeruginosa with a ZOI of 17 mm. Conclusion: Based on the findings of this study, it can be concluded that utilizing Coelastrella terrestris algae for the synthesis of CuO NPs presents a promising solution for addressing environmental contamination.

Phyco-synthesis of silver nanoparticles by environmentally safe approach and their applications.

In recent years, there has been an increasing interest in the green synthesis of metallic nanoparticles, mostly because of the evident limitations associated with chemical and physical methods. Green synthesis, commonly referred to as "biogenic synthesis," is seen as an alternative approach to produce AgNPs (silver nanoparticles). The current work focuses on the use of Asterarcys sp. (microalga) for biological reduction of AgNO3 to produce AgNPs. The optimal parameters for the reduction of AgNPs were determined as molarity of 3 mM for AgNO3 and an incubation duration of 24 h at pH 9, using a 20:80 ratio of algal extract to AgNO3. The biosynthesized Ast-AgNPs were characterised using ultraviolet-visible spectroscopy (UV-Vis), zeta potential, scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), and high-resolution transmission electron microscopy (HR-TEM) with selected area electron diffraction (SAED) patterns. The nanoparticles exhibited their highest absorption in the UV-visible spectra at 425 nm. The X-ray diffraction (XRD) investigation indicated the presence of characteristic peaks at certain angles: 38.30° (1 1 1), 44.40° (2 0 0), 64.64° (2 2 0), and 77.59° (3 1 1) according to the JCPDS file No. 04-0783. Based on SEM and TEM, the Ast-AgNPs had an average size of 35 nm and 52 nm, respectively. The zeta potential was determined to be - 20.8 mV, indicating their stability. The highest antibacterial effectiveness is shown against Staphylococcus aureus, with a zone of inhibition of 25.66 ± 1.52 mm at 250 µL/mL conc. of Ast-AgNPs. Likewise, Ast-AgNPs significantly suppressed the growth of Fusarium sp. and Curvularia sp. by 78.22% and 85.05%, respectively, at 150 µL/mL conc. of Ast-AgNPs. In addition, the Ast-AgNPs exhibited significant photocatalytic activity in degrading methylene blue (MB), achieving an 88.59% degradation in 120 min, revealing multiple downstream applications of Ast-AgNPs.

Asterarcys quadricellulare algae-mediated copper oxide nanoparticles as a robust and recyclable catalyst for the degradation of noxious dyes from wastewater.

The present article explores the synthesis of copper oxide nanoparticles (CuO NPs) utilizing Asterarcys quadricellulare algal extract and examines the effect of various reaction parameters on the size and morphology of the nanoparticles. The samples were thoroughly characterized using XRD, FTIR, UV-vis, FE-SEM, and EDS techniques. The XRD analysis disclosed that the size of the synthesized nanoparticles could be controlled by adjusting the reaction parameters, ranging from 4.76 nm to 13.70 nm along the highest intensity plane (111). FTIR spectroscopy provided evidence that the phytochemicals are present in the algal extract. We have compared the photocatalytic activity of biologically and chemically synthesized CuO NPs and observed that biologically synthesized CuO NPs showed better photocatalytic activity than chemically synthesized CuO NPs. The biosynthesized CuO NPs (S8) demonstrated outstanding photodegradation activity towards four different organic dyes, namely BBY, BG, EBT, and MG, with degradation percentages of 95.78%, 98.02%, 94.15%, and 96.04%, respectively. The maximum degradation efficacy of 98.02% was observed for the BG dye at optimized reaction conditions and 60 min of visible light exposure. The kinetics of the photodegradation reaction followed the pseudo-first-order kinetic model, and the rate constant (k) was calculated using the Langmuir-Hinshelwood model for each dye. This study provides an efficient and sustainable approach for synthesizing CuO NPs with superior photocatalytic degradation efficiency towards organic dyes.

Evaluation of uranium content and annual ingestion dose in the surface and ground water bodies of Chittorgarh, Rajasthan, India.

Uranium, naturally occurring radionuclide is chemotoxic and nephrotoxic beyond acceptable limit. The presence of uranium beyond acceptable limit in surface and ground water, adversely affecting people's health. In the present investigation, the uranium concentration in surface and ground water of Chittorgarh, Rajasthan was studied along with the physico-chemical parameters of water (n = 87). The ground water was further sub-categorised into well water, handpump water, and borewell water. The mean uranium concentration was observed at 2.5 ± 1.9 µgL-1 and 16.5 ± 1.4 µgL-1 in the surface and ground water samples, respectively. In sub-categories of ground water, the highest uranium concentration was found in borewell water (23.3 ± 17.0 µgL-1), followed by handpump water (13.5 ± 9.1 µgL-1) and well water (6.0 ± 5.5 µgL-1). The uranium concentration was correlated significantly with the depth of the ground water table. It also correlated significantly with electrical conductivity, total dissolved solids and nitrate concentration. 100% of surface water and 88.9% of ground water samples carried uranium concentration within the acceptable limit of WHO (30 µgL-1). The annual ingestion dose was found at 3.8 µSvy-1 (for males) and 2.8 µSvy-1 (for females) in surface water and 25.4 µSvy-1 (for males) and 18.5 µSvy-1 (for females) in ground water. In the sub-categories of the ground water sample, the annual ingestion dose followed the trend in males 35.8 µSvy-1 (borewell water) > 20.7 µSvy-1 (hand pump water) > 9.2 µSvy-1 (well water) and in females 26.1 µSvy-1 (borewell water) > 15.1 µSvy-1 (hand pump water) > 6.7 µSvy-1 (well water).

Recent Trends in Photocatalytic Enantioselective Reactions.

Enantioselective synthesis through photocatalysis is one of the highly preferred approaches towards preparation of optically active compounds. This review elaborates and critically analyzes the different strategies of photocatalytic enantioselective reactions through H-bonding, transition metal catalysis, phase-transfer catalysis (PTC), chiral Lewis acid catalysis, N-heterocyclic carbene catalysis, and amine catalysis, and also explores ion pairs. In addition, it explains the different catalysis modes with multifunctional approaches for enantioselective photocatalytic reactions.

COVID-19 lockdown: a boon in boosting the air quality of major Indian Metropolitan Cities.

ABSTRACT: The COVID-19 lockdown has not only helped in combating the community transmission of SARS-CoV-2 but also improved air quality in a very emphatic manner in most of the countries. In India, the first phase of COVID-19 lockdown came into force on March 25, 2020, which was later continued in the next phases. The purpose of this study was to investigate the result of lockdown on air quality of major metropolitan cities-Delhi, Mumbai, Kolkata, Chennai, Bengaluru, Hyderabad, Jaipur, and Lucknow-from March 25 to May 3, 2020. For this study, the concentration of six criteria air pollutants (PM2.5, PM10, CO, NO2, SO2, and O3) and air quality index during the COVID-19 lockdown period was compared with the same period of the previous year 2019. The results indicate a substantial improvement in air quality with a drastic decrease in the concentration of PM2.5, PM10, CO, and NO2, while there is a moderate reduction in SO2 and O3 concentration. During the lockdown period, the maximum reduction in the concentration of PM2.5, PM10, CO, NO2, SO2, and O3 was observed to be - 49% (Lucknow), - 57% (Delhi), - 75% (Mumbai), - 68% (Kolkata), - 48% (Mumbai), and - 29% (Hyderabad), respectively. The value of the air quality index (AQI) also dwindled significantly during the COVID-19 lockdown period. The maximum decline in AQI was observed - 52% in Bengaluru and Lucknow. The order of AQI was satisfactory > moderate > good > poor and the frequency order of prominent pollutants was O3 > PM10 > PM2.5 > CO > NO2 > SO2 during the lockdown period in all the aforementioned metropolitan cities.

Generating Stereodiversity: Diastereoselective Fluorination and Highly Diastereoselective Epimerization of α-Amino Acid Building Blocks.

Diastereoselective fluorination of N-Boc ( R)- and ( S)-2,2-dimethyl-4-((arylsulfonyl)methyl)oxazolidines and a previously unknown diastereoselective epimerization at the fluorine-bearing carbon atom α to the sulfone was realized. Diastereoselectivities of both reactions were excellent for benzothiazolyl sulfones, allowing access to two enantiomerically pure diastereomers from one chiral precursor. To demonstrate synthetic utility, the benzothiazolyl sulfones were converted to diastereomerically pure ( S, S)- and ( R, S)-benzyl sulfones via sulfinate salts and to amino acids. To understand the diastereoselectivities, DFT analysis was performed.