Photocatalytic investigation of textile dyes and E. coli bacteria from wastewater using Fe3O4@MnO2 heterojunction and investigation for hydrogen generation on NaBH4 hydrolysis.

Various impurities found nowadays in water can be detrimental to human health. This work focused on utilizing Fe3O4@MnO2 nanocomposite for cleaning organic contaminants from water, including rhodamine B (RhB) and Escherichia coli (E. coli). Analysis methods such as XRD, UV-vis, TEM, and FTIR were used to describe the nanocomposite. The results showed that the developed nanocomposite has good photocatalytic activity against pollutants in wastewater. The E. coli was destroyed after 90 min, and the RhB photodegradation rate was 75%. Moreover, the Fe3O4@MnO2 efficiency as a catalyst for producing hydrogen as an alternative energy source was tested. According to the calculations, the nanomaterial's turnover frequency, activation energy, enthalpy, and entropy are 1061.3 h-1, 28.93 kJ/mol, 26.38 kJ/mol, and -128.41 J/mol.K, respectively. Four reusability tests were completed, and the average reusability was 78%. The obtained data indicated the excellent potential for the developed Fe3O4@MnO2 nanomaterial to act as an adsorbent, thus representing an alternative to the classical depollution methods. This study showed that nanoparticles have a photocatalytic effect against pathogenic bacteria and RhB azo dye in polluted waters and offer an effective catalytic activity to produce hydrogen as an alternative energy source.

One-step synthesized biogenic nanoparticles using Linum usitatissimum: Application of sun-light photocatalytic, biological activity and electrochemical H2O2 sensor.

This study aimed to synthesize Ag NPs as a green catalyst for photocatalytic activity and to examine their biological activities. It was determined that they have high activity in catalytic and biological activities. The green synthesis which is an environmentally friendly and inexpensive method was used to synthesize Ag-NPs using Linum usitatissimum as a reducing agent. Transmission electron microscopy (TEM), infrared to Fourier transform infrared (FTIR) spectroscopy, UV-Visible (UV-Vis) spectroscopy, and X-ray diffraction (XRD) were used to characterize the Ag NPs. In UV-Vis examination, Ag-NPs had intense peaks in the 435 nm region. The antibacterial activity of Ag NPs was investigated, and Ag NPs showed a high lethal effect against S. aureus, E. coli, B. subtilis, and MRSA. In addition, Ag NPs were tested for anticancer activity against the HT-29 colon cancer cell line, MDA-MB-231 breast cancer cell line, healthy cell line L929-Murine Fibroblast cell Lines, and MIA PaCa-2 human pancreatic cancer cell line at various concentrations (1-160 µg/mL) and showed a high anticancerogenic properties against MDA-MB-231 cells. Ag NPs showed the ability of DNA cleavage activity. Also, the antioxidant activity of Ag NPs against DPPH was found to be 80% approximately. Furthermore, the photocatalytic activity of Ag NPs against methylene blue (MB) was determined to be 67.13% at the 180th min. In addition, it was observed that biogenic Ag NPs have high electrocatalytic activity for hydrogen peroxide (H2O2) detection. In the sensor based on Ag NPs, linearity from 1 µM to 5 µM was observed with a detection limit (LOD) of 1.323 µM for H2O2. According to these results, we conclude that the biogenic Ag NPs synthesized using Linum usitatissimum extract can be developed as an efficient biological agent as an antibacterial and anticancer also can be used as a photocatalyst for industrial wastewater treatment to prevent wastewater pollution.

Facile bio-fabrication of ZnO@AC nanoparticles from chitosan: Characterization, hydrogen generation, and photocatalytic properties.

In this work, activated carbon-supported zinc oxide nanoparticles (ZnO@AC NPs) were studied using the thermal synthesis method. The activated carbon-supported zinc oxide catalyst was characterized by UV-Vis spectrometry techniques, Fourier Transform Infrared Spectrophotometer (FTIR), Transmissive electron microscopy (TEM), and X-ray diffraction (XRD) methods. XRD characterization measurements showed that the average size of the crystal NPs was 6.89 nm. According to the TEM analysis results, the nanoparticles' average size was 11.411 nm, and the particles had a spherical structure. The catalytic properties of the synthesized material were determined using the sodium borohydride methanolysis reaction. A kinetic study was performed regarding the effects of temperature, catalyst, and substrate concentration on the methanolysis reaction. Reusability experiments showed that the catalyst had excellent catalytic activity (85%), stability, and selectivity. As a result of the kinetic study, activation energy, enthalpy (ΔH), entropy (ΔS), and hydrogen production rate activation parameters were found to be 42.52 kJ/mol, 39.98 kJ/mol, -181.42 J/mol.K, 1257.69 mL/min. g, respectively. Also, the photocatalytic activity of ZnO@AC NPs was analyzed against Rhodamine B (RhB) dye, and the maximum degradation percentage was observed to be 76% at 120 min. This study aimed to develop the ZnO@AC NPs into an efficient photocatalyst to prevent industrial wastewater pollution and as a catalyst for hydrogen synthesis as an alternative energy source.

Biosynthesis of Ag-Pt bimetallic nanoparticles using propolis extract: Antibacterial effects and catalytic activity on NaBH4 hydrolysis.

The critical environmental issues of antibiotic resistance and renewable energies supply urge researching materials synthesis and catalyst activity on hydrogen production processes. Aiming to analyse the antibacterial effect of platinum-silver (Ag-Pt) nanoparticles (NPs) and the catalyst effect on NaBH4 hydrolysis that can be used for hydrogen generation technology, in this work, Ag-Pt NPs were prepared using aqueous propolis extract. Various methods were used for the characterization (Uv-vis Spectroscopy, Transmission Electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FTIR), Atomic Force Microscopy (AFM) and X-ray diffraction Spectroscopy (XRD)). The antimicrobial activity of Ag-Pt bimetallic nanoparticles was evaluated in vitro by the microdilution method against Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Staphylococcus epidermidis, and Serratia marcescens. The results confirmed the antimicrobial activity of bimetallic NPs Ag-Pt concentrations of (25, 50, and 100 µg/ml). A concentration of 100 µg/ml showed low bacterial viability varying between 22.58% and 29.67% for the six tested bacteria. For the catalyst activity on NaBH4 hydrolysis, the results showed high turnover factor (TOF) and low activation energy of 1208.57 h-1 and 25.61 kJ/mol, respectively, with high hydrogen yield under low temperature. Synthesized Ag-Pt NPs can have great potential for biological and hydrogen storage applications.

Enhanced photocatalytic performance of auto-combusted nanoparticles for photocatalytic degradation of azo dye under sunlight illumination and hydrogen fuel production.

In this study, an innovative nanomaterial was synthesized for hydrogen production from methanolysis on sodium borohydride (NaBH4) in order to be a solution for future energy problems. The nanocomposite containing FeCo, which does not contain noble metals, and whose support material is Polyvinylpyrrolidone (PVP), was synthesized by means of a thermal method. TEM, XRD and FTIR characterization methods were used for the analysis of the morphological and chemical structure of the nanocomposite. Nanocomposite particle size was found to be 2.59 nm according to XRD analysis, and 5.45 nm according to TEM analysis for scale of 50 nm. For catalytic properties of nanomaterial in the methanolysis reaction of NaBH4, temperature, catalyst, substrate, and reusability experiments were carried out and kinetic calculations were obtained. Among the activation parameters of FeCo@PVP nanoparticles, turnover frequency, enthalpy, entropy and activation energy were calculated as 3858.9 min-1, 29.39 kJ/mol, -139.7 J/mol.K, and 31.93 kJ/mol, respectively. As a result of the reusability test of the obtained FeCo@PVP nanoparticles catalysts, which was carried out for 4 cycles, the catalytic activity was 77%. Catalytic activity results are given in comparison with the literature. In addition, the photocatalytic activity of FeCo@PVP NPs was evaluated against MB azo dye under solar light irradiation for 75 min and was found to be as 94%.

Carbon supported Pd based catalysts for the hydrolytic dehydrogeneration of morpholine borane.

Although the reducing property of morpholine borane is frequently used, there are few studies on its use as a chemical hydrogen storage material. This study presents the catalyst efficiency for hydrogen production in the dehydrogenation reaction of morpholine borane as efficient and cost-effective hydrogen storage material, which can be used as an alternative to depleting fossil fuels. It was studied with four different catalysts as activated Carbon-supported Pd, PdAg, PdNi, and PdCo. Bimetallic palladium based catalysts were used for the dehydrogenation of morpholine borane for the first time. Nanoparticles were synthesized using the chemical reduction method. The catalytic effects of different metal ratios of PdNi/C nanoparticles, which were concluded to have the best catalyst effect, were investigated and it was observed that the ratio of Pd50Ni50/C nanoparticles exhibited better catalytic behavior, and optimization studies were carried out with Pd50Ni50/C nanoparticles. Transmission Electron Microscopy, X-Ray Diffraction, and X-Ray Photoelectron Spectroscopy analyzes were performed for the characterization of nanoparticles. According to the characterization analyzes of Pd50Ni50/C nanoparticles, the mean particle size was determined as 2.0 ± 1.0 nm. Catalyst efficiency was determined by performing the substrate, catalyst, and temperature experiments separately in the dehydrogenation reaction of Morpholine Borane. These parameters are respectively; Ea and ΔH were calculated as 93.2 kJ/mol, and 90.6 kJ/mol. The reusability experiments were carried out in 4 cycles. In other words, with this study, it was concluded that the reusability of Pd50Ni50/C nanoparticles synthesized by the chemical method is high and their catalytic activity is excellent.

Phyto-mediated synthesis of nanoparticles and their applications on hydrogen generation on NaBH4, biological activities and photodegradation on azo dyes: Development of machine learning model.

This work reports the synthesis of the silver-platinum bimetallic nanoparticles (N@Pt-Ag BNPs) reduced by an ethanolic extract of black seed (Nigella sativa, N) using the green synthesis method, these nanoparticles show a great antibacterial, anticancer, and catalytic activity. The characterization of physicochemical properties of Ag-Pt BNP was carried out using UV-visible spectroscopy (Uv-vis), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Transmission electron microscope (TEM) analysis. The structural morphology shows that the N@Pt-Ag BNPs are spherical particles with a diameter of 5.6 nm. The cytotoxic effects of N@Pt-Ag BNPs were examined by MTT test in human breast cancer, human colon cancer, human pancreatic cancer, L929-Murine fibroblast cells. N@Pt-Ag BNPs have been observed to be much more effective in breast cancer cell lines. The cytotoxic effect of N@Pt-Ag BNPs against healthy L929-murine fibroblast cell lines was not observed. Also, high antibacterial activity on each of the bacteria Escherichia coli (E. coli), Bacillus subtilis (B. subtilis), Methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus aureus (S. aureus), where we note that most strains of E. coli and S. aureus were damaged with a 73% percentage, 67% bacterial inhibition respectively. The results of the catalytic activities of N@Pt-Ag BNPs were obtained by performing the hydrolysis experiments of sodium borohydride (NaBH4). According to the results obtained, TOF, enthalpy, entropy, and activation energy, values were found to be 2497.14 h-1, 13.52 kJ/mol, -137.47 J/mol.K, 16.02 kJ/mol, respectively. N@Pt-Ag BNPs were found to be highly effective catalysts for hydrogen production which this was also confirmed by the machine learning model. The photocatalytic activity of N@Pt-Ag BNPs was tested against methylene blue (MB) dye and the highest activity was found as 80%.

An ultra-sensitive rifampicin electrochemical sensor based on Fe3O4 nanoparticles anchored Multiwalled Carbon nanotube modified glassy carbon electrode.

This study aimed to guide future sensor studies against other pharmaceutical drugs by synthesizing Fe3O4NPs@MWCNT metallic nanoparticles (NPs). Side damage caused by excessive accumulation of tuberculosis drugs in the body can cause clots in the organs, and cause serious damage such as heart attack and respiratory failure, and threaten human life. Therefore, the development of sensors sensitive to various antibiotics in this study is important for human health. In this study, the sensitivity of Fe3O4 NPs to tuberculosis drug (rifampicin) was evaluated by catalytic reaction using bare/GCE, MWCNT/GCE, and Fe3O4NPs@MWCNT/GCE electrodes. First of all, Fe3O4 NPs were successfully synthesized for the study and MWCNT/GCE and Fe3O4 NPs@MWCNT/GCE electrodes were formed with the modification of the MWCNT support material. It was observed that the Fe3O4 NPs@MWCNT/GCE electrode gave the highest signal against the other electrodes. The morphological structure of Fe3O4 NPs was determined by various characterization techniques such as Transmission Electron Microscopy (TEM), Fourier Transmission Infrared Spectroscopy (FTIR), ultraviolet-visible (UV-Vis), and X-ray differential (XRD) and the obtained NPs were used for sensor studies, and it was observed that the current intensity increased as the scanning speed of each electrode increased in CV and DPV measurements. The average size of Fe3O4 NPs was found to be 7.32 ± 3.2 nm. Anodic current peaks occurred in the linear range of 2-25 µM. According to the results obtained from the measurements, the limit of detection (LOD) value was calculated as 0.64 µM limit of quantification (LOQ) 1.92 µM.

Toxicological effects of some antiparasitic drugs on equine liver glutathione S-Transferase enzyme activity.

Benzimidazoles are antiparasitic drugs having an extensive application field like agriculture, medicine, and especially in veterinary medicine. In this study, we report the effect of some benzimidazole drugs such as ricobendazole (RBZ), thiabendazole (TBZ), albendazole (ALBA) and oxfendazole (OFZ) on glutathione s-transferase (GST) enzyme activity. The kinetics studies, IC50 and Ki values of the tested drugs on GSTs enzyme activity were investigated. The obtained ranking of IC50 values were found to be approximately RBZ (53.31 µM, r2: 0.9778) < OFZ (57.75 µM, r2: 0.9630) < ALBA (63.00 µM, r2: 0.9443) < TBZ (69.30 µM, r2: 0.9491). And the obtained ranking of Ki values of the tested drugs (RBZ, TBZ, ALBA, and OFZ) for GSTs enzyme activity was found to be approximately 26.37 ±â€¯2.96, 44.01 ±â€¯5.74, 39.82 ±â€¯3.98 and 30.14 ±â€¯3.03 µM, respectively. Experimental results showed that tested the benzimidazoles drugs have some significant inhibitory effect on GSTs enzyme activity. And also, it was determined that RBZ, ALBA, OFZ are competitive inhibition, but TBZ is non-competitive inhibitors on GSTs enzyme activity. RBZ drug showed the best inhibitory effect with the lowest Ki value.

Biological synthesis of silver nanoparticles using Rheum ribes and evaluation of their anticarcinogenic and antimicrobial potential: A novel approach in phytonanotechnology.

This paper reports the anticarcinogenic and antimicrobial properties of silver nanoparticles (Ag NPs) obtained by green synthesis using the extract of Rheum ribes (R. ribes), a medicinal plant. For the synthesis of Ag NPs, the ethanolic extracts of R. ribes were used as a reducing as well as the stabilizing agent. For the characterization of Ag NPs, advanced analytical methods such as transmission electron microscopy (TEM), X-Ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and UV-vis spectrophotometry were performed. The synthesized Ag NPs obtained from R. ribes were evaluated as a cytotoxic agent against MDA-MB-231 breast carcinoma cell line. The IC50 values of the nanoparticles were ranged from 165 to 99 µg/mL against MDA-MB 231 cell line for 24 h and 48 h, respectively. The results show that the use of Ag NPs at low concentrations show the toxic effect in the cancer cells. In addition, the results of experiments on gram-positive (Staphylococcus aureus (S. aureus), Methicillin-resistant Staphylococcus aureus (MRSA) and Bacillus subtilis (B. subtilis)) and gram-negative (Escherichia coli (E. coli)) bacteria showed that the Ag NPs had high antimicrobial activity. The results suggest that Ag NPs can be developed as potential anticancer and antibacterial agents.

Biogenic platinum nanoparticles using black cumin seed and their potential usage as antimicrobial and anticancer agent.

Herein, the biogenic platinum nanoparticles (Pt NPs) were synthesized by using black cumin seed (Nigella sativa L.) extract as a reducing agent. The biogenic platinum nanoparticles synthesized by black cumin seed extract was characterized in detail by Transmission Electron Microscopy (TEM), UV-vis spectrophotometer, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS). According to TEM analysis, Pt nanoparticles have spherical shapes and sizes between 1-6 nm. Moreover, the biogenic Pt NPs was assessed for its cytotoxicity effect on MDA-MB-231 breast and HeLa cervical cancer lines and their antibacterial effect against selected strains of gram-positive and negative bacteria. The cytotoxicity and bacterial tests showed the effectiveness of biogenic Pt nanoparticles. Dose-dependent toxicity effects were shown in the MDA-MB-231 breast and HeLa cervical cancer lines (IC50: 36.86 µg/mL and 19.83 µg/mL, respectively). In addition, Pt NPs showed high zone diameters against gram-positive and gram-negative bacteria at concentrations of 100 and 500 µg/ml. These results contribute to the development of the pharmaceutical industry as a potential antibacterial and anticancer agent.

Synthesis and characterization of Rosa canina-mediated biogenic silver nanoparticles for anti-oxidant, antibacterial, antifungal, and DNA cleavage activities.

In biomedical applications, silver nanoparticles (Ag NPs) are of great interest due to their cost-effective and environmentally friendly properties. Green synthesis of nanoparticles for biological research is a preferred choice since it does not require additional reducing agent. For this purpose, in this study, we aimed to synthesize the biogenic silver nanoparticles with the help of Rosa canina plant (Rc-Ag NPs) and then they have been tried for their antioxidant and antibacterial properties. UV-Vis spectrophotometer, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analyses were performed for characterization of Rc-Ag NPs. Antioxidant properties of silver nanoparticles synthesized with Rosa canina plant were investigated against 2,2'-diphenyl-1-picrylhydrazyl radical (DPPH). DNA dissociation activity of synthesized Rc-Ag NPs was studied, and DNA dissociation activity was shown. The antimicrobial activity of Rc-Ag NPs was also tested using micro-dilution. According to the results, Rc-Ag NPs synthesized were found to be highly effective for anti-oxidant, antibacterial, antifungal, and DNA cleavage activities.

Composites of Bimetallic Platinum-Cobalt Alloy Nanoparticles and Reduced Graphene Oxide for Electrochemical Determination of Ascorbic Acid, Dopamine, and Uric Acid.

The ultimate aim of this study is to produce a composite of bimetallic platinum-cobalt nanoparticles and reduced graphene oxide (Pt-Co@rGO) based biosensor for the detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA). Those are biologically important molecules with the key functions for the human body. Pt-Co@rGO was synthesized using a microwave-assisted technique and utilized for the production of a highly sensitive and stable electrochemical biosensor. Detailed spectral XPS and Raman analysis, XRD, and TEM/HR-TEM characterization were also studied. Due to the superior activity and excellent conductivity of rGO, well-separated oxidation peaks of these biomolecules is proven by DPV (differential pulse voltammetry) and CV (cyclic voltammetry) measurements. The prepared Pt-Co@rGO-based biosensor showed high electrochemical activity, a broad linear response, high sensitivity, and acceptable limit of detection values for individual and simultaneous determination of AA, DA, and UA, under optimized conditions. The linear range of Pt-Co@rGO was found to be 170-200; 35-1500 and 5-800 µM for AA, DA, and UA, respectively. Moreover, the detection limit of the prepared composite was calculated as 0.345; 0.051; 0.172 µM for AA, DA, and UA, respectively. In the field of electrochemical biosensors, Pt-Co@rGO based sensor is highly promising due to its superior sensitivity and good selectivity properties.