Enhancement in the visible light induced photocatalytic and antibacterial properties of titanium dioxide codoped with cobalt and sulfur.

In this study, the sol-gel technique was used to develop Cobalt Sulfur codoped Titanium Dioxide (Co-S codoped TiO2) photocatalysts. For structural analysis of the prepared resultant TiO2 samples, XRD, FTIR, UV-Vis DRS, SEM, HR-TEM and EDX measurements were used to describe the produced photocatalysts. The characterization findings indicate that the synthesized nanoparticles possessed great crystallinity, high purity, and superior optical characteristics. For the methylene blue (MB) degradation process, Co-S codoped TiO2 nanoparticles were tested for their photocatalytic degradation performance. The Co-S codoped TiO2 nanoparticles had improved catalytic activity when compared with pure, Co-doped, S-doped TiO2 and decomposed 93% of MB in 120 min. When compared to pure and doped TiO2, the catalysts of Co-S codoped TiO2 showed a synergistic effect and improved the performance of the catalysts. Furthermore, the antibacterial applications of synthesized Co-S codoped TiO2 nanoparticles was studied against E. coli (Gram negative) and S. aureus (Gram positive) bacteria and exhibited strong antibacterial activity against the selected strains.

Constructing Z-scheme g-C3N4/TiO2 heterostructure for promoting degradation of the hazardous dye pollutants.

The use of dyes and segments has increased widely in recent years, but it poses a serious health risk to ecosystems. In this work, TiO2 and two-dimensional g-C3N4 nanosheets (g-CN) were fabricated through co-precipitation and thermal polymerization technique, respectively. The g-CN-TiO2 photocatalyst (1: 3, 2: 2, 3: 1) in various weight percentages was prepared using a simple impregnation process. The photocatalytic behaviour of the g-CN, TiO2 NPs, and different weight percentages of g-CN-TiO2 photocatalyst was evaluated against methylene blue (MB) dye under UV-visible light illumination. Compared to pristine and other weight percentages of the g-CN-TiO2 nanocomposite, the optimized g-CN-TiO2 nanocomposite (3:1) showed promoted performance against MB dye. The enriched catalytic efficiency can be accredited to the low amount of TiO2 nanoparticles deposited on gCN nanosheets, possibly due to the boosted transport properties of the electron-hole pairs. The enriched photocatalytic behaviour can be attributed to the development of the Z-scheme system between TiO2 and g-CN. The current study is an outstanding demonstration of the development of maximum catalytic efficiency for destroying hazardous chemical dyes.

Bioremediations analysis using multifactorial porous materials derived from tea residue.

Titanium dioxide nanoparticles (TiO2 NPs) are becoming more and more renowned as biocompatible nanomaterials with diverse biological functions. In the present study, the aqueous extract of tea residue (tea filtered waste powder) was used to synthesize the TiO2 NPs and treated for effluent bioremediations. Maximum absorption in the UV-Vis spectrum of the TiO2 NPs was seen at 358 nm, and the XRD pattern reveals peaks at 2 h values of 25.78, 38.24, 47.98, 54.76, 55.32, 62.64, 69.05, 70.15, 75.24, and 83.59 that may be indexed to the (101), (004), (200), (105), (211), (204), (116), (220), (215) and (303). The FT-IR spectra of TiO2 NPs showed a peak at 3420, 2925, 1621, 1382, 1098, and 687 cm-1. The spherical form and size were disclosed by FE-SEM analyses, and the EDAX pattern verified the purity of the TiO2 NPs. The average particles size of the TiO2 NPs was 32 nm. The photodegradation of paper mill waste water is significantly deteriorated up to 99.08% for 600 min, but textile waste water is degraded up to 98.06% for the same duration. Furthermore, we reported that TiO2 NPs may rapidly breakdown industrially hazardous effluents when exposed to sunshine. Overall, this new, straightforward, and environmentally beneficial strategy may be of interest to the management of efficient degradation of dye solutions in the polluted regions.

Facile construction of cost-effective zinc-aluminium polymeric framework for efficient removal of selective both drug and dye from an aqueous medium.

A novel aluminium (Al) and its active alloys are extensively been used in nearly all areas owing to their cost-effectiveness. But when it is subjected to an aqueous medium, gets corroded through a chemical response. In this paper, a novel framework was fabricated by copolymer coating over on Al and loaded with zinc via electro polymerization and electrodeposition method ([EDA- OPDA]Al@Zn). The as-fabricated composite has emerged for the sorption of Methylene Blue (MB) aqueous dye and Paracetomal drug (PAR). The as-fabricated composite framework has been categorized via IR spectra, FE-SEM images, and EDX spectra. The sorption progression was optimized for numerous prompting features like pH, contact time and impact of dosage. Based on kinetics data, the growth in QE value by an enhancement in temperature for adsorption and the higher r values shows the adsorption progression is a pseudo-second-order model. The thermodynamic constraints specify that the field of adsorbate is impulsive and typical endothermic process. Instead, the corrosion resistance of a composite in the 3.5% of NaCl. Solution was explored via EIS spectra and potentio-dynamic polarization. Depending on the observed features, it indicates that the [EDA-OPDA]Al@Zn framework provided fantastic corrosion resistance. So it is obvious that the as-synthesized framework is of multitasking, that it could be successfully performed for the exclusion of MB aqueous dye and PAR drug from the aqueous medium and it also withstands effectively in this corrosive medium.

Synthesizing Ag2Ox(3 wt%)-loaded ZnFe2O4 photocatalysts for efficiently saving polluted aquatic ecosystems.

Herein, we report an Ag2Ox (3 wt%)-loaded ZnFe2O4 photocatalysts synthesized by co-precipitation and incipient wet impregnation approach for acetamiprid degradation, antibacterial, antioxidant, and toxicity assay. Initially, bare ZnFe2O4 nanostructures were made through a simple co-precipitation method. In the second step, 3 wt% of various transition metal oxides (CuOx, ZrOx, and Ag2Ox) were embedded on the surface of ZnFe2O4 photocatalysts via a wet impregnation method. Further, the prepared photocatalysts were systematically characterized using XRD, FTIR, FE-SEM, BET, HRTEM, and XPS analysis. The optimum Ag2Ox (3 wt%)-loaded ZnFe2O4 photocatalysts revealed higher degradation efficiencies for acetamiprid under sunlight irradiation. Additionally, the Ag2Ox (3 wt%)-loaded ZnFe2O4 photocatalysts showed more effective antioxidant and antibacterial activity than blank and bare ZnFe2O4 nanomaterials. The enriched catalytic efficiency can be accredited to the 3 wt% of Ag2Ox NPs loaded on ZnFe2O4 nanomaterials, possibly due to the boosted transport properties of the electron-hole pairs. This study will provide a new avenue for the development of simple and effective photocatalysts for efficiently saving polluted aquatic ecosystems.

Visible light active hybrid silver decorated g-C3N4-CeO2 nanocomposite for ultrafast photocatalytic activity and toxicity evaluation.

Development of hybrid graphitic carbon nitride (GCN) nanocomposite is an emerging research area in wastewater treatment. Herein, hybrid visible light active photocatalyst of silver decorated polymeric graphitic carbon nitride and (Ag-GCN) with cerium oxide (CeO2) nanocomposite was prepared and characterized in detail. The Ag-GCN/CeO2 photocatalyst has successfully prepared by an electrostatic self-assembly approach. The synthesized Ag-GCN/CeO2 NCs photocatalysts are characterized by various physio-chemical techniques. Using the Ag-GCN/CeO2 catalyst, the excellent photodegradation efficiency of Acid yellow-36 (AY-36) and Direct yellow-12 (DY-12) dye solution were achieved 100% within 150 min sun light irradiation. The Ag-GCN/CeO2 rate constant values of 0.048 and 0.046/min has been determined for AY-36 and DR-12 dyes, respectively. The extraordinary photocatalytic activity is due to incorporation of CeO2 with Ag-GCN which play a significant role in visible light absorption, superior reactive oxygen generation (ROS) and excellent pollutant catalyst interaction. The toxicity of the photocatalytically degraded AY-36 and DR-12 dyes were measured using the soil nematode Caenorhabditis elegans, a well-established in vivo model in biology, by analyzing survival, physiological functions, intracellular ROS levels, and stress-protective gene expressions.

Design of 1,4-Dihydropyridine Hybrid Benzamide Derivatives: Synthesis and Evaluation of Analgesic Activity and Their Molecular Docking Studies.

Purpose: This study aims to determine the analgesic activity of 1,4-dihydropyridine hybrid benzamide derivatives. These hybrid derivatives were synthesized, and their analgesic activity was studied. The synthesis method applied was a one-step reaction involving a green chemistry approach. Methods: The compounds were prepared via the amination method with a yield ranging between 82% and 93%. The title compounds were confirmed by means of IR, 1H and 13C NMR, and mass spectral analyses. The pharmacological activity of all the synthesized compounds was evaluated, and the analgesic activities were monitored in vivo (by tail immersion methods), with a digital analgesiometer. The drug response and damage of tail ata concentration of 10 mg/kg were measured by tail-flicking latency. Results: The activity of compound 2c (81.35% activity at 5mg/kg) can be correlated with its salicylamidemoiety (13.99% activity at 5mg/kg), and diclofenac showed comparable activity (79.21% activity at 5mg/kg reference drugs). Compound 2c has a higher potential to inhibit COX proteins compared to diclofenac. The drug-like nature of the molecule 2c corresponds to its ADME properties. Conclusion: In this study, all the synthesized compounds were found to possess significant analgesic activities; particularly, the performance of compound 2c is excellent. Thus, the preparative method described is an apt route for developing novel therapeutic formulations.

Pollutant removal from cheese processing effluent using effective indigenous natural scavengers.

The goal of this study was to come up with an efficient method for treating cheese production wastewater. Because the effluent has a higher concentration of organic and inorganic materials, the indigenous microbial treatment process was used to effectively remove total dissolved solids (TDS), chemical oxygen demand (COD), and color without the addition of any nutrients. The indigenous microorganisms were tested for color, TDS, and COD elimination by growing them in "nutrient broth medium" loaded with different amounts of cheese effluent. The isolates were identified by 16S rRNA sequencing, and the results revealed that strain 1 was Enterobacter cloacae, strain 2 was Lactococcus garvieae, and strains 3 and 4 were Bacillus cereus and Bacillus mycoides, respectively. After 36 h of incubation, the data were evaluated. Among all the microbes, E. cloacae reduced TDS and COD from the effluent the most (80 ± 0.2% and 87 ± 0.4% COD, respectively). When compared to individual species, consortia were more efficient (86 ± 0.2% TDS and 90 ± 0.3% COD). On treatment, the correlation coefficient "r" for TDS and COD elimination was found to be 1, resulting in a positive linear connection. The current study suggests that microbial therapies are both effective and environmentally beneficial.