In situ preparation of TiO2/f-MWCNT catalyst using Pluronic F127 assisted sol-gel process for sonocatalytic degradation of methylene blue.

In this study, titanium dioxide- Pluronics @F127/functionalized -multi walled carbon nanotubes (TiO2-F127f-/MWCNT) nanocatalysts were prepared, characterized, and used in methylene blue (MB) degradation under ultrasonic conditions. The characterization studies were performed using TEM, SEM, and XRD analyses to reveal the morphological and chemical properties of TiO2-F127/MWCNT nanocatalysts. To detect the optimum parameters for MB degradation using TiO2-F127/f-MWCNT nanocatalysts, several experimental parameters were conducted at various conditions such as different temperatures, pH, catalyst amount, hydrogen peroxide (H2O2) concentration, and various reaction contents. Transmission electron microscopy (TEM) analyses showed that TiO2-F127/f-MWCNT nanocatalysts consisted of a homogenous structure and have a 12.23 nm particle size. The crystalline particle size of TiO2-F127/MWCNT nanocatalysts was found to be 13.31 nm. Scanning electron microscope (SEM) analyses revealed the surface structure of TiO2-F127/f-MWCNT nanocatalysts turned to be modified after TiO2 loaded on MWCNT. Under the optimum conditions; pH: 4, MB concentration: 25 mg/L, H2O2 concentration: 30 mol/L, reaction time: and catalyst dose: 24 mg/L, chemical oxygen demand (COD) removal efficiency reached a maximum of 92%. To detect the radical effectiveness, three scavenger solvents were tested. Reuse experiments revealed that TiO2-F127/f-MWCNT nanocatalysts retained 84.2% catalytical activity after 5 cycles. Gas chromatography-mass spectrometry (GC-MS) was successfully used to identify the generated intermediates. Based on the experimental results, it has been suggested that •OH radicals are the main active species responsible for the degradation reaction in the presence of the TiO2-F127/f-MWCNT nanocatalysts.

Has PdCu@GO effect on oxidant/antioxidant balance? Using zebrafish embryos and larvae as a model.

Industrial products containing PdCu@GO can gain access to the aquaculture environment, causing dangerous effects on living biota. In this study, the developmental toxicity of zebrafish treated with different concentrations (50, 100, 250, 500 and 1000 µg/L) of PdCu@GO was investigated. The findings showed that PdCu@GO administration decreased the hatchability and survival rate, caused dose-dependent cardiac malformation. Reactive oxygen species (ROS) and apoptosis were also inhibited in a dose-dependent manner, with acetylcholinesterase (AChE) activity affected by nano-Pd exposure. As evidence for oxidative stress, malondialdehyde (MDA) level increased and superoxide dismutase (SOD), catalase (CAT) glutathione peroxidase (GPx) activities and glutathione (GSH) level decreased due to the increase in PdCu@GO concentration. Our research, it was determined that the oxidative stress stimulated by the increase in the concentration of PdCu@GO in zebrafish caused apoptosis (Caspase-3) and DNA damage (8-OHdG). Stimulation of ROS, inflammatory cytokines, tumor Necrosis Factor Alfa (TNF-α) and interleukin - 6 (IL-6), which act as signaling molecules to trigger proinflammatory cytokine production, induced zebrafish immunotoxicity. However, it was determined that the increase of ROS induced teratogenicity through the induction of nuclear factor erythroid 2 level (Nrf-2), NF-κB and apoptotic signaling pathways triggered by oxidative stress. Taken together with the research findings, the study contributed to a comprehensive assessment of the toxicological profile of PdCu@GO by investigating the effects on zebrafish embryonic development and potential molecular mechanisms.

Synthesis and application of AuNi@AC nano adsorbents for the removal of Maxilon Blue 5G azo dye from aquatic mediums.

In this research, gold-nicel supported on activated carbon (AC) nanoadsorbent (AuNi@AC) synthesized by following a series of physicochemical procedures was prepared for the removal of Maxilon Blue 5G (MB) which is a cationic textile dye. Experimental studies based on parameters specifically pH, contact time, nano catalytic adsorbent particle, initial MB dye concentration and temperature effect were conducted in aqueous solutions in a batch system. AuNi@AC nanoadsorbents (NAs) reached the equilibrium in 30 min under optimum conditions in adsorption of the dye. The pseudo-first, second-order, and intra-particle diffusion models were tested to evaluate a the experimental results. Adsorption kinetics were found to be represented by the pseudo-second-order model, and the maximum adsorption capacity (qmax.) was calculated to be 542.90 mg/g (or 2.041 mmol/g). The synthesized magnetic AuNi@AC nanoadsorbent showed a high-efficiency reusability effect of about 64% after five reuse runs. Also, thermodynamic function parameters such as activation energy (Ea), Gibbs free energy (ΔG *), and entropy (ΔS *) were investigated in the sorption study. After all evaluation of data, it was concluded that the novel AuNi@AC nanoadsorbent could be considered as an effective support material for the removal of various organic pollutants in aquation solution especially for the removal of MB.

Fabrication of activated carbon supported modified with bimetallic-platin ruthenium nano sorbent for removal of azo dye from aqueous media using enhanced ultrasonic wave.

Herein, activated carbon supported modified with bimetallic-platin ruthenium nano sorbent (PtRu@AC) was synthesized by a thermal decomposition process and used in the removal of methylene blue (MB) from aqueous solutions. The synthesized nano sorbents were characterized by X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM), and X-ray Photoelectron Spectroscopy (XPS) spectroscopic techniques. The data obtained from characterization studies showed that PtRu@AC nano sorbent was highly crystalline and in a form of PtRu alloy with a monodispersed composition. The results indicated that the maximum adsorption capacity (qemax) for the removal of MB with PtRu@AC under optimum conditions was detected to be 1.788 mmol/g (569.4 mg/g). The experimental kinetic results of the study revealed that the adsorption of methylene blue was found to be more compatible with the false second-order model compared to some tested models. Calculations for thermodynamic functions including enthalpy change (ΔHo), entropy change (ΔSo), and Gibbs free energy change (ΔGo) values were performed to get an idea about the adsorption mechanism. As a result, the synthesized PtRu@AC nano adsorbent was detected as a highly effective adsorbent material in the removal of MB from aquatic mediums.

Investigation of the Oxidative Stress Response of a Green Synthesis Nanoparticle (RP-Ag/ACNPs) in Zebrafish.

Silver nanoparticles (AgNPs) are prominent nanomaterials that are efficiently used in different industries including medical products, water treatment, and cosmetics. However, AgNPs are known to cause adverse effects on the ecosystem and human health. In this study, aqueous extract of Rumex patientia (RP) was used as a reducing and stabilizing agent in AgNP biosynthesis. The obtained activated carbon (AC) from Chenopodium album (CA) plant was combined with RP-AgNPs to synthesize RP-Ag/AC NPs. Next, the effects of these green synthesis RP-Ag/AC NPs on zebrafish (Danio rerio) embryos and larvae were investigated. First, we characterized the RP-Ag/AC NPs by using X-ray diffraction (XRD) and transmission electron microscopy (TEM) and determined LC50 value as 217.23 mg/L at 96 h. Next, the alterations in survival rate, hatching rate, and morphology of the larvae at 96 h were monitored. The survival rates decreased in a dose-dependent manner. Morphological defects such as yolk sac edema, pericardial edema, spinal curvature, and tail malformation in the NP-treated larvae were observed. RP-Ag/AC NPs stimulated the production of neuronal NOS (nNOS) and 8-OHdG in zebrafish brain tissues in a dose-dependent manner and enhanced neutrophil degeneration and necrosis at concentrations of 50 and 100 mg/L. Thus, the obtained data suggest that the green synthesis process is not sufficient to reduce the effect of oxidative stress caused by AgNPs on oxidative signaling.

Ecotoxicological Effects of Bimetallic PdNi/MWCNT and PdCu/MWCNT Nanoparticles onto DNA Damage and Oxidative Stress in Earthworms.

Bimetallic nanoparticles are synthesized using two different metal elements and used recently in many fields. However, limited studies related to the ecotoxic effects of nanoparticles available in the literature. The purpose of this study is to synthesize and characterize bimetallic PdCu/MWCNT and PdNi/MWCNT NPs and investigate their ecotoxic effects on earthworms. For this purpose, we injected approximately 20 µL of various concentrations of bimetallic PdCu/MWCNT and PdNi/MWCNT NPs (1, 10, 100, 1000, and 2000 mg/L) into the coelomic space of earthworms. We evaluated survival rate, malformations, reactive oxygen species (ROS) level, 8-OHdG content, and histopathological changes in earthworms at the 48th hour after exposure. PdCu/MWCNT and PdNi/MWCNT NPs were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD) pattern, and Raman-scattering spectroscopy. Toxicological examinations showed that PdCu/MWCNT NPs reduced the survival rate of earthworms (2000 mg/L, 84%) and caused various malformations (various lesions, thinning, swelling, and rupture), but nonsignificant effects of survival rate and malformations were observed in earthworms using PdNi/MWCNT NPs. The histopathological examinations of earthworm tissues exposed with PdNi/MWCNT determined that tissues in all treatment groups had a normal histological appearance. However, at a concentration of 2000 mg/L of PdCu/MWCNT NPs, atrophy in the longitudinal muscle layer and less degenerative cells in the epidermis layer were observed in earthworm tissues. It was determined that PdNi/MWCNT and PdCu/MWCNT NPs caused significant increases in ROS levels and 8-OHdG activity in earthworm tissues after 48 h. Finally, our results demonstrated that the toxicity of PdNi/MWCNT NPs was detected to be lower than PdCu/MWCNT NPs. However, both nanoparticles may pose a toxicological risk at high concentrations (1000 and 2000 mg/L). These findings will provide valuable information to studies on the use of PdNi/MWCNT NPs in wastewater treatment systems, industrial and medical fields, which have been determined to have less ecotoxicological risk.

Textile dyes Maxilon blue 5G and Reactive blue 203 induce acute toxicity and DNA damage during embryonic development of Danio rerio.

Common textile dyes used in various industrial sectors are organic compounds and considered for the aquatic environment as pollutants. The textile dye industry is one of the main sectors that have serious impacts on the environment due to a large amount of wastewater released into the ecosystem. Maxilon blue 5G (MB-5G) and Reactive Blue 203 (RB-203) are widely used textile dyes. However, their potential toxicity on living organisms remains to be elucidated. Here, we investigate the acute toxicity and genotoxicity of MB-5G and RB-203 dyes using the zebrafish embryos/larvae. Embryos treated with each dye for 96 h revealed LC50 values of acute toxicity as 166.04 mg L-1 and 278.32 mg L-1 for MB-5G and RB 203, respectively. When exposed to MB-5G and RB-203 at different concentrations (1, 10, and 100 mg L-1) for 96 h, the expression of 8-hydroxy-2'-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage, significantly increased in brain tissues as compared to control. MB-5G and RB-203 resulted in common developmental abnormalities including tail malformation, microphthalmia, pericardial edema, curved body axis, and yolk sac/pericardial edemas. Moreover, at its highest dose (100 mg L-1), RB-203 caused premature hatching after 48 h, while MG-5G did not. Our results collectively reveal that the textile dyes MB-5G and RB-203 cause genotoxicity and teratogenicity during embryonic and larval development of zebrafish. Thus, it is necessary to eliminate these compounds from wastewater or reduce their concentrations to safe levels before discharging the textile industry wastewater into the environment.

Palladium supported on polypyrrole/reduced graphene oxide nanoparticles for simultaneous biosensing application of ascorbic acid, dopamine, and uric acid.

In this study, we report a facile and effective production process of palladium nanoparticles supported on polypyrrole/reduced graphene oxide (rGO/Pd@PPy NPs). A novel electrochemical sensor was fabricated by incorporation of the prepared NPs onto glassy carbon electrode (GCE) for the simultaneous detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA). The electrodes modified with rGO/Pd@PPy NPs were well decorated on the GCE and exhibited superior catalytic activity and conductivity for the detection of these molecules with higher current and oxidation peak intensities. Simultaneous detection of these molecules was achieved due to the high selectivity and sensitivity of rGO/Pd@PPy NPs. For each biomolecule, well-separated voltammetric peaks were obtained at the modified electrode in cyclic voltammetry (CV) and differential pulse voltammetry (DPV) measurements. Additionally, the detection of these molecules was performed in blood serum samples with satisfying results. The detection limits and calibration curves for AA, DA, and UA were found to be 4.9 × 10-8, 5.6 × 10-8, 4.7 × 10-8 M (S/N = 3) and ranging from 1 × 10-3 to 1.5 × 10-2 M (in 0.1 M PBS, pH 3.0), respectively. Hereby, the fabricated rGO/Pd@PPy NPs can be used with high reproducibility, selectivity, and catalytic activity for the development of electrochemical applications for the simultaneous detection of these biomolecules.

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.

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.

Magnetic nanocomposites decorated on multiwalled carbon nanotube for removal of Maxilon Blue 5G using the sono-Fenton method.

Herein, multiwalled carbon nanotube-based Fe3O4 nano-adsorbents (Fe3O4@MWCNT) were synthesized by ultrasonic reduction method. The synthesized nano-adsorbent (Fe3O4@MWCNT) exhibited efficient sonocatalytic activity to remove Maxilon Blue 5G, a textile dye, and present in a cationic form, in aqueous solution under ultrasonic irradiation. The magnetic nano-adsorbent particles were characterized by high-resolution transmission electron microscopy (HR-TEM), transmission electron microscopy (TEM), Raman spectroscopy and X-ray diffraction (XRD). Some important parameters such as nano-adsorbent dosage, solution pH, initial dye and H2O2 concentration, reaction time, ultrasonic power and temperature were tested to determine the optimum conditions for the elimination of Maxilon Blue 5G dye. The reusability results showed that Fe3O4@MWCNT nano-adsorbent has a decrease of about 32.15% in the removal efficiency of Maxilon Blue 5G under ultrasonic irradiation after six times reuse. Additionally, in order to reveal the sufficient kinetic explanation, various experiments were performed at different temperatures and testing three kinetic models like the pseudo-first-order, pseudo-second-order and intraparticle diffusion for removal adsorption process of Maxilon Blue 5G using Fe3O4@MWCNT nano-adsorbent. The experimental kinetic results revealed that the adsorption process of Maxilon Blue 5G in the aquatic mediums using sono-Fenton method was found to be compatible with the intraparticle diffusion. Using kinetic models and studies, some activation parameters like enthalpy, entropy and Gibbs free energy for the adsorption process were calculated. The activation parameters indicated that Fe3O4@MWCNT nano-adsorbent could be used as an effective adsorbent for the removal of Maxilon Blue 5G as a textile dye and the adsorption process of Maxilon Blue 5G with Fe3O4@MWCNT nano-adsorbent is spontaneous.

Multiwalled carbon nanotube-based nanosensor for ultrasensitive detection of uric acid, dopamine, and ascorbic acid.

A novel multiwalled carbon nanotube (MWCNT) based sensor was fabricated as a highly precise and stable electrochemical sensor. The synthesized sensor which consists of ZnNi bimetallic nanoalloy called the ZnNi NPs@f-MWCNT sensor, have been used for the simultaneous detection of uric acid (UA), dopamine (DA) and ascorbic acid (AA). The ZnNi NPs@f-MWCNT sensor obtained based on the microwave irradiation process, and its characterization was performed by using several physical techniques such as XRD, XPS, TEM, Raman, etc. The characterization showed that this sensor has excellent properties such as rich pore channels, excellent structural durability, and large surface area. These properties facilitated mass transfer and electron conductions. It was observed that the obtained sensor gave high electrochemical activity and wide linear responses (0.3-1.1 mM AA, 0.2-1.2 mM DA, 0.2-1.1 mM UA) in the detection of uric acid (UA), dopamine (DA) and ascorbic acid (AA). In addition to these properties, it has been found that the sensor has excellent anti-interferents properties towards AlCl3, KCl3, glucose, etc. and ZnNi NPs@f-MWCNT sensor was further applied to determine uric acid (UA), dopamine (DA) and ascorbic acid (AA) in real samples.