Comprehensive assessment of carbon-, biomaterial- and inorganic-based adsorbents for the removal of the most hazardous heavy metal ions from wastewater.

Owing to the high cost of recycling waste, underdeveloped countries discharge industrial, agricultural, and anthropogenic effluents without pretreatment. As a result, pollutant-loaded waste enters water bodies. Among the diverse toxic contaminants, heavy metal ions are the most detrimental because of their chronic toxicity, non-degradability, prevalence, and bioaccumulation. The growing shortage of water resources demands the removal of heavy metal ions from wastewater. Three SDGs of the sustainability agenda of the United Nations appeal for clean water to protect life beneath water and on land depending on the water sources. Therefore, efficient environmentally friendly approaches for wastewater treatment are urgently required. In this regard, several methods have been developed for the removal of heavy metal ions from wastewater, including adsorption as the most widely used method owing to its eco-friendly, cost-effective, and sustainable nature. The present review discusses the progress in the preparation and application of various adsorbents based on carbon, micro-organisms, agricultural waste and inorganic materials for the extraction of toxic metal ions such as Pb2+, Cr6+, As3+, As5+, Hg2+ and Cd2+. Herein, we provide information on the role of the homogeneity and heterogeneity of adsorbents, kinetics of the adsorption of an adsorbate on the surface of an adsorbent, insights into adsorption reaction pathways, the mechanism of the sorption process, and the uptake of solutes from solution. The present review will be useful for researchers working on environmental protection and clean environment.

Metal-Based Nanomaterials for the Sensing of NSAIDS.

Cadmium sulfide and zinc oxide nanoparticles were prepared, characterized and used as electrode modifiers for the sensing of two non-steroidal anti-inflammatory drugs (NSAIDs): naproxen and mobic. The structural and morphological characterization of the synthesized nanoparticles was carried out by XRD, UV-Vis spectroscopy, FTIR and scanning electron microscopy. The electrode's enhanced surface area facilitated the signal amplification of the selected NSAIDs. The CdS-modified glassy carbon electrode (GCE) enhanced the electro-oxidation signals of naproxen to four times that of the bare GCE, while the ZnO-modified GCE led to a two-fold enhancement in the electro-oxidation signals of mobic. The oxidation of both NSAIDs occurred in a pH-dependent manner, suggesting the involvement of protons in their electron transfer reactions. The experimental conditions for the sensing of naproxen and mobic were optimized and, under optimized conditions, the modified electrode surface demonstrated the qualities of sensitivity and selectivity, and a fast responsiveness to the target NSAIDs.

Nanostructured Design Cathode Materials for Magnesium-Ion Batteries.

Energy is undeniably one of the most fundamental requirements of the current generation. Solar and wind energy are sustainable and renewable energy sources; however, their unpredictability points to the development of energy storage systems (ESSs). There has been a substantial increase in the use of batteries, particularly lithium-ion batteries (LIBs), as ESSs. However, low rate capability and degradation due to electric load in long-range electric vehicles are pushing LIBs to their limits. As alternative ESSs, magnesium-ion batteries (MIBs) possess promising properties and advantages. Cathode materials play a crucial role in MIBs. In this regard, a variety of cathode materials, including Mn-based, Se-based, vanadium- and vanadium oxide-based, S-based, and Mg2+-containing cathodes, have been investigated by experimental and theoretical techniques. Results reveal that the discharge capacity, capacity retention, and cycle life of cathode materials need improvement. Nevertheless, maintaining the long-term stability of the electrode-electrolyte interface during high-voltage operation continues to be a hurdle in the execution of MIBs, despite the continuous research in this field. The current Review mainly focuses on the most recent nanostructured-design cathode materials in an attempt to draw attention to MIBs and promote the investigation of suitable cathode materials for this promising energy storage device.

Study on the association and phase separation behavior of surfactants and promethazine hydrochloride: impact of ammonium electrolytes.

In the current study, the association and phase separation of cationic tetradecyltrimethylammonium bromide (TTAB) and nonionic Triton X-100 (TX-100) surfactants with promethazine hydrochloride (PMH) were investigated in aqueous ammonium-based solutions. The micellization nature of the TTAB and PMH drug mixture was examined by evaluating critical micelle concentration (CMC) and counterion binding extent (ß) at different salt contents and temperatures (298.15-323.15 K). Micelle formation in the TTAB + PMH mixture was enhanced in the presence of ammonium salts, whereas the process was delayed with an increase in temperature in the respective salt solution. With an increase in salt content, the cloud point (CP) of the TX-100 + PMH mixture decreased, which revealed that the respective progression occurred through the salting out phenomenon. In micellization and clouding processes, the changes in free energies ΔG0m and ΔG0c were found to be negative and positive, respectively, demonstrating that the corresponding processes are spontaneous and non-spontaneous. Standard enthalpies (ΔH0m/ΔH0c) and standard entropies (ΔS0m/ΔS0c) for the association and clouding processes, respectively, were also calculated and discussed. The core forces amid TTAB/TX-100 and PMH in the manifestation of electrolytes are dipole-dipole and hydrophobic forces among the employed components according to the values for ΔH0m/ΔH0c and ΔS0m/ΔS0c, respectively.

Electrochemical detection and removal of brilliant blue dye via photocatalytic degradation and adsorption using phyto-synthesized nanoparticles.

Herein, we report a sensitive electrochemical platform prepared by modifying the electrode surface with copper-doped zinc oxide nanoparticles; these nanoparticles were prepared via a green synthetic approach using the extract of Cassia fistula leaves and multiwalled carbon nanotubes (MWCNTs). For the best response of the electrode modifier, a number of experimental conditions were optimized to obtain the most intense signal of the target analyte Coomassie brilliant blue using a rapid analysis technique square wave voltammetry. The designed sensor displayed remarkable sensitivity for Coomassie brilliant blue with a detection limit of 0.1 nM under the optimized conditions. Moreover, the repeatability, specificity and reproducibility of the designed sensor demonstrated its potential for practical applications. The sensing platform was also used for monitoring the degradation kinetics of the Coomassie brilliant blue dye. Catalytic degradation of the dye was performed using the synergistic effect of Cu-ZnO NPs together with Fenton reagent. The dye degraded by 96% in 60 minutes under neutral conditions, which is one of the main achievements of this work that has never been reported. The photocatalytic breakdown of Coomassie brilliant blue was also monitored using UV-visible spectroscopy. The degradation kinetics results of both techniques agreed well. The adsorption of Coomassie brilliant blue using ZnO NPs was monitored spectrophotometrically. The adsorption data were fitted in a pseudo-second order kinetic model by following the Langmuir isotherm at lower concentration and Freundlich isotherm at higher concentration.

Neem plant extract-assisted synthesis of CeO2 nanoparticles for photocatalytic degradation of piroxicam and naproxen.

Piroxicam and naproxen are well-known non-steroidal anti-inflammatory drugs that are frequently detected in aquatic environments due to their widespread usage and improper disposal practices. This research investigates the photocatalytic degradation of these drugs by using CeO2 nanoparticles. The nanoparticles were synthesized by using Azadirachta indica plant extract and were characterized through various characterization techniques such as UV-visible spectroscopy, FTIR spectroscopy, SEM, EDX, and XRD. The photocatalytic degradation of piroxicam and naproxen using CeO2 nanoparticles led to the efficient removal of these pharmaceutical drugs in a short time duration with photodegradation efficiencies of 89% and 97% for naproxen and piroxicam, respectively. The photodegradation reaction was found to follow pseudo-order first-order kinetics. The recyclability of the catalyst was also studied for up to six cycles where the degradation efficiency was maintained at 100% till the 2nd cycle and was decreased by 11 and 13% for piroxicam and naproxen respectively after the 6th cycle. The current work focused on the achievement of sustainable development goals (SDGs) for water purification via environmentally benign nanoparticles to remedy water pollution as it is the most prevalent issue in developed and underdeveloped countries throughout the world.

Photoelectrocatalytic Detection and Degradation Studies of a Hazardous Textile Dye Safranin T.

Herein, we report an electrochemical scaffold consisting of functionalized multiwalled carbon nanotubes (COOH-fMWCNTs) and iron-doped zinc oxide nanoparticles (Fe-ZnO) for the detection of a hazardous textile dye safranin T (ST) and monitoring of its photocatalytic degradation. Prior to the detection and degradation analysis, Fe-ZnO NPs were synthesized by the sol-gel method and characterized by a number of structural and morphological techniques. The carboxyl moiety of COOH-fMWCNTs possessing a strong affinity for the amino functionality of ST led to significant enhancement of the current response at the designed electrochemical platform, whereas the electrocatalytic role, surface area enhancement, and the provision of binding sites of Fe-ZnO led to a further increase in the peak current intensity of ST. Electrochemical impedance spectroscopy showed that the sensing scaffold made of the glassy carbon electrode modified with COOH-fMWCNTs and Fe-ZnO efficiently transfers charge between the transducer and the redox probe. Under optimized conditions, the developed sensor showed a 2.3 nM limit of detection for ST. Moreover, recovery experiments and anti-interference tests qualified the sensing platform for practical applications. The dye was photocatalytically degraded using Fe-ZnO NPs up to 99% in 60 min with a rate constant of 0.068 min-1. The designed sensor was used to probe the degradation kinetics of the target dye, and the results were found consistent with the findings obtained from electronic absorption method. To the best of our knowledge, the present work is the first approach for the efficient detection and almost absolute degradation of ST.

Eucalyptus globulus Mediated Green Synthesis of Environmentally Benign Metal Based Nanostructures: A Review.

The progress in nanotechnology has effectively tackled and overcome numerous global issues, including climate change, environmental contamination, and various lethal diseases. The nanostructures being a vital part of nanotechnology have been synthesized employing different physicochemical methods. However, these methods are expensive, polluting, eco-unfriendly, and produce toxic byproducts. Green chemistry having exceptional attributes, such as cost-effectiveness, non-toxicity, higher stability, environment friendliness, ability to control size and shape, and superior performance, has emerged as a promising alternative to address the drawbacks of conventional approaches. Plant extracts are recognized as the best option for the biosynthesis of nanoparticles due to adherence to the environmentally benign route and sustainability agenda 2030 of the United Nations. In recent decades, phytosynthesized nanoparticles have gained much attention for different scientific applications. Eucalyptus globulus (blue gum) is an evergreen plant belonging to the family Myrtaceae, which is the targeted point of this review article. Herein, we mainly focus on the fabrication of nanoparticles, such as zinc oxide, copper oxide, iron oxide, lanthanum oxide, titanium dioxide, magnesium oxide, lead oxide, nickel oxide, gold, silver, and zirconium oxide, by utilizing Eucalyptus globulus extract and its essential oils. This review article aims to provide an overview of the synthesis, characterization results, and biomedical applications of nanoparticles synthesized using Eucalyptus globulus. The present study will be a better contribution to the readers and the students of environmental research.

Photocatalytic Degradation of Food and Juices Dyes via Photocatalytic Nanomaterials Synthesized through Green Synthetic Route: A Systematic Review.

The unavailability of non-poisonous and hygienic food substances is the most challenging issue of the modern era. The uncontrolled usage of toxic colorant moieties in cosmetics and food manufacturing units leads to major threats to human life. The selection of environmentally benign approaches for the removal of these toxic dyes has gained the utmost attention from researchers in recent decades. This review article's main aim is the focus on the application of green-synthesized nanoparticles (NPs) for the photocatalytic degradation of toxic food dyes. The use of synthetic dyes in the food industry is a growing concern due to their harmful effects on human health and the environment. In recent years, photocatalytic degradation has emerged as an effective and eco-friendly method for the removal of these dyes from wastewater. This review discusses the various types of green-synthesized NPs that have been used for photocatalytic degradation (without the production of any secondary pollutant), including metal and metal oxide NPs. It also highlights the synthesis methods, characterization techniques, and photocatalytic efficiency of these NPs. Furthermore, the review explores the mechanisms involved in the photocatalytic degradation of toxic food dyes using green-synthesized NPs. Different factors that responsible for the photodegradation, are also highlighted. Advantages and disadvantages, as well as economic cost, are also discussed briefly. This review will be advantageous for the readers because it covers all aspects of dyes photodegradation. The future feature and limitations are also part of this review article. Overall, this review provides valuable insights into the potential of green-synthesized NPs as a promising alternative for the removal of toxic food dyes from wastewater.

Advancements in Nanofiber-Based Electrochemical Biosensors for Diagnostic Applications.

Biosensors are analytical tools that can be used as simple, real-time, and effective devices in clinical diagnosis, food analysis, and environmental monitoring. Nanoscale functional materials possess unique properties such as a large surface-to-volume ratio, making them useful for biomedical diagnostic purposes. Nanoengineering has resulted in the increased use of nanoscale functional materials in biosensors. Various types of nanostructures i.e., 0D, 1D, 2D, and 3D, have been intensively employed to enhance biosensor selectivity, limit of detection, sensitivity, and speed of response time to display results. In particular, carbon nanotubes and nanofibers have been extensively employed in electrochemical biosensors, which have become an interdisciplinary frontier between material science and viral disease detection. This review provides an overview of the current research activities in nanofiber-based electrochemical biosensors for diagnostic purposes. The clinical applications of these nanobiosensors are also highlighted, along with a discussion of the future directions for these materials in diagnostics. The aim of this review is to stimulate a broader interest in developing nanofiber-based electrochemical biosensors and improving their applications in disease diagnosis. In this review, we summarize some of the most recent advances achieved in point of care (PoC) electrochemical biosensor applications, focusing on new materials and modifiers enabling biorecognition that have led to improved sensitivity, specificity, stability, and response time.

Elucidating the interaction of antidepressant drug paroxetine with ct-dsDNA: A comparative study by electrochemical, spectroscopic, and molecular docking approaches.

This study is designed to investigate the interaction of phenylpiperidine derivative drug paroxetine, which is an effective serotonin reuptake inhibitor and biomolecules through electrochemical, fluorescence spectroscopy, and molecular docking methods. The interaction between paroxetine and biomolecules was investigated by differential pulse voltammetry according to the decrease in deoxyguanosine anodic oxidation signal of double-stranded calf thymus DNA. Fluorescence spectroscopy studies were performed by titrating paroxetine against double-stranded calf thymus DNA solution at four different temperatures. The fluorescent results showed that paroxetine had a great affinity to bind with double-stranded calf thymus DNA. Interaction studies demonstrate that paroxetine binds to double-stranded calf thymus DNA via intercalation binding mode, and the binding constant values ​​were calculated as 7.24 × 104 M-1 and 1.52 × 104 M-1 at 25 °C, based on voltammetric and spectroscopic results, respectively. Moreover, with the aim of elucidating the interaction mechanism between paroxetine and double-stranded calf thymus DNA, electrochemical and fluorescence spectroscopy studies along with molecular docking analysis were made.

Electrochemical Sensor for Detection and Degradation Studies of Ethyl Violet Dye.

In this work, a simple and sensitive electrochemical method was developed to determine ethyl violet (EV) dye in aqueous systems by using square wave anodic stripping voltammetry (SWASV) employing a glassy carbon electrode modified with acidic-functionalized carbon nanotubes (COOH-fCNTs). In square wave anodic stripping voltammetry, EV exhibited a well-defined oxidation peak at 0.86 V at the modified GCE. Impedance spectroscopy and cyclic voltammetry were used to examine the charge transduction and sensing capabilities of the modified electrode. The influence of pH, deposition potential, and accumulation time on the electro-oxidation of EV was optimized. Under the optimum experimental conditions, the limit of detection with a value of 0.36 nM demonstrates high sensitivity of COOH-fCNTs/GCE for EV. After detection, it was envisioned to devise a method for the efficient removal of EV from an aqueous system. In this regard a photocatalytic degradation method of EV using Ho/TiO2 nanoparticles was developed. The Ho/TiO2 nanoparticles synthesized by the sol-gel method were characterized by UV-vis, XRD, FTIR, SEM, and EDX. The photocatalytic degradation studies revealed that basic medium is more suitable for a higher degradation rate of EV than acidic and neutral media. The photodegradation kinetic parameters were evaluated using UV-vis spectroscopic and electrochemical methods. The results revealed that the degradation process of EV follows first-order kinetics.

Anti-Alzheimer and Antioxidant Effects of Nelumbo nucifera L. Alkaloids, Nuciferine and Norcoclaurine in Alloxan-Induced Diabetic Albino Rats.

The present study is aimed to determine the efficacy and dose response of the nuciferine (1), norcoclaurine (2) and crude extract of Nelumbo nucifera in managements of diabetes, Alzheimer disease and related allergies. Experimentally, alloxan (100 mg/kg body weight (b.w.))-induced diabetic rats (200−250 g) were divided into seven groups (n = 6). Group I: normal control, Group II: diabetic control, Group III: standard treated with glibenclamide and Group lV-VII: treated with methanolic crude extracts (100, 200 mg/kg), nuciferine and norcoclaurine (10 mg/kg b.w.) for 15 days. Different tests were performed, including blood glucose, body weights and antioxidant enzyme assays, i.e., superoxide dismutase (SOD), catalase test (CAT), lipid peroxidation assay (TBARS), glutathione assay (GSH) and acetylcholinesterase (AChE) assay. Nuciferine and norcoclaurine significantly reduced blood glucose (p < 0.05) and restored body weight in diabetic rats. Moreover, nuciferine and norcoclaurine (10 mg/kg) significantly recovered the antioxidant enzymes (SOD, CAT, GPx and GSH) which decreased during induced diabetes. Significant increase in TBARS was also observed in the diabetic group and nuciferine as well as norcoclaurine (10 mg/kg) inhibited the increase in TBARS in diabetic animals (p < 0.05), as compared to glibenclamide. AChE activity was significantly recovered by nuciferine and norcoclaurine (10 mg/kg) both in the blood and brain of the diabetic group (p < 0.05). Nuciferine and norcoclaurine showed potent inhibitory effects against α-glucosidase and α-amylase with IC50, 19.06 ± 0.03, 15.03 ± 0.09 µM and 24.07 ± 0.05, 18.04 ± 0.021 µM, as confirmed by molecular docking studies. This study concludes that nuciferine and norcoclaurine significantly improve memory and could be considered as an effective phytomedicine for diabetes, Alzheimer's disease (AD) and oxidative stress.

Electrochemical Sensing Platform Based on Functionalized Multi-Walled Carbon Nanotubes and Metal Oxide for the Detection and Degradation Studies of Orange II Dye.

Textile industry effluents are heavily contaminated with dyes. The discharge of these toxic dyes into waterbodies poses a serious threat to aquatic flora and fauna. The ultimate entrance of these toxins from thereon into the food chain affects the primary and secondary consumers. Therefore, the adoption of a sustainable solution for protection against the detrimental effects associated with adulterated water is an immediate need of the hour. To address the severity of the issue, the present work aims to design an electrochemical sensing platform by modifying the glassy carbon electrode (GCE) with zinc oxide nanoparticles and amino group-functionalized multi-walled carbon nanotubes (NH2-fMWCNTs) for the detection of Orange II, which is a toxic azo dye. Zinc oxide nanoparticles facilitate electron transfer between the transducer and the analyte. While, the positively charged NH2-fMWCNTs in acidic medium help in preconcentration of negatively charged analyte molecules at the electrode/electrolyte interface. The modification of the GCE catalyzed the oxidation of Orange II, as evidenced by the negative shift of the oxidation potential and enhancement in peak current intensity. Square wave voltammetry was used to optimize various experimental conditions, such as the supporting electrolyte, pH of the electrolyte, deposition potential, and deposition time for the best performance of the designed sensor. Under the optimized conditions, the detection limit and quantification of the designed sensor were found to be 0.57 and 1.92 nM, respectively. The catalytic degradation studies of Orange II was shown to be facilitated by titanium dioxide, which acted as a photocatalyst. The addition of hydrogen peroxide further promoted the extent and rate of degradation of dye. The breakdown of Orange II was probed by the designed sensing platform electrochemically and also by UV-visible spectroscopy. The dye degraded up to 92% by following pseudo-first-order kinetics.

Efficacy and Safety of a Long-Term Multidisciplinary Weight Loss Intervention under Hospitalization in Aging Patients with Obesity: An Open Label Study.

The effects of the hypocaloric diet under hospitalization on blood biochemical parameters (lipid, glycaemic, thyroid and liver profiles) were not reported in literature. This study aims to evaluate the efficacy and safety of a hypocaloric diet under hospitalisation in obese patients. A total of 151 obese subjects (49 males and 102 females, aged 69.38 ± 14.1 years, BMI 41.78 ± 7.1) were enrolled in this study. Participants were treated with an hypocaloric diet for a maximum period of 3 months. Outcomes were assessed at the beginning and at the end of the recovery period. The average duration of the hospitalisation was 47.5 days ± 1.3. The effect of the diet on all the outcomes was evaluated using the Analysis of Covariance (ANCOVA) and the predictors of weight loss were identified using linear regression. The diet induced a reduction in the anthropometric (BMI decrease of -2.713 points) and DXA body measurements in addition to serum lipids, glucose, Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) and C-reactive protein (CRP) levels without affecting the muscle mass, liver and thyroid profiles. During the intervention, there was a positive shift in body composition favouring fat free mass (FFM). Lower insulin but higher serum calcium and potassium levels were predictors of weight loss.

Development of Electrolyzer Using NiCo(OH)2 Layered Double Hydroxide Catalyst for Efficient Water Oxidation Reaction.

Over the past decade, layered double hydroxides (LDH) have been the subject of extensive investigations owing to their remarkable water splitting catalytic activity. Stability and porosity are several of the features of LDH which help them to serve as efficient oxygen evolution reaction (OER) catalysts. Based on these considerations, we synthesized NiCo(OH)2 LDH and probed its OER electrocatalytic performance. The synthesized catalyst was subjected to X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy for structural analysis and investigation of its surface morphology, surface composition, and oxidation states. The LDH-NiCo(OH)2 was anchored over the FTO surface and the fabricated electrode was found to exhibit a much lower OER onset potential of 265 mV, a much higher current density of 300 mAcm-2 and a smaller Tafel slope of 41 mVdec-1. Moreover, the designed catalyst was found to be stable up to 2500 repeated voltametric scans. These figures of merit regarding the structure and performance of the designed LDH are expected to provide useful insights into the fundamental understanding of the OER catalysts and their mechanisms of action, thus enabling the more rational design of cost effective and highly efficient electrocatalysts for use in water splitting.

A designed miniature sensor for the trace level detection and degradation studies of the toxic dye Rhodamine B.

The presence of organic pollutants in water and food samples is a risk for the environment. To avoid this hazard a variety of analytical tools are used for the detection of toxic organic contaminants. Herein we present a selective and sensitive electrochemical sensor based on amino group functionalized multi walled carbon nanotubes and carboxylic group functionalized multi walled carbon nanotubes (HOOC-fMWCNTs/NH2-fMWCNTs) as modifiers of the glassy carbon electrode for the detection of a toxic dye, Rhodamine B. The sensing ability of the designed sensor was examined by electrochemical impedance spectroscopy, cyclic voltammetry and square wave voltammetry. The synergistic effect of HOOC-fMWCNTs and NH2-fMWCNTs (layer by layer) led to enhanced electrocatalytic activity of the modified electrode surface for Rhodamine B detection. Under optimized conditions, the graph between concentration and peak current followed a linear trend in the concentration range of 0.1 nM to 0.05 µM. The limits of detection and quantification were found to be 57.4 pM and 191.3 pM respectively. The designed sensor was also used for probing the degradation of Rhodamine B. Sodium borohydride was found to degrade Rhodamine B in neutral media under ambient conditions. The kinetics of degradation followed first order kinetics. Rhodamine B degraded to the extent of more than 80% as revealed by electrochemical and spectrophotometric techniques. The developed method is promising for the treatment of dye contaminated wastewater. Moreover, it uses only a microliter volume of the sample for analysis.

Conversion of Polypropylene Waste into Value-Added Products: A Greener Approach.

Plastic has made our lives comfortable as a result of its widespread use in today's world due to its low cost, longevity, adaptability, light weight and hardness; however, at the same time, it has made our lives miserable due to its non-biodegradable nature, which has resulted in environmental pollution. Therefore, the focus of this research work was on an environmentally friendly process. This research work investigated the decomposition of polypropylene waste using florisil as the catalyst in a salt bath over a temperature range of 350-430 °C. A maximum oil yield of 57.41% was recovered at 410 °C and a 40 min reaction time. The oil collected from the decomposition of polypropylene waste was examined using gas chromatography-mass spectrometry (GC-MS). The kinetic parameters of the reaction process were calculated from thermogravimetric data at temperature program rates of 3, 12, 20 and 30 °C·min-1 using the Ozawa-Flynn-Wall (OFW) and Kissinger-Akahira-Sunnose (KAS) equations. The activation energy (Ea) and pre-exponential factor (A) for the thermo-catalytic degradation of polypropylene waste were observed in the range of 102.74-173.08 kJ·mol-1 and 7.1 × 108-9.3 × 1011 min-1 for the OFW method and 99.77-166.28 kJ·mol-1 and 1.1 × 108-5.3 × 1011 min-1 for the KAS method at a percent conversion (α) of 0.1 to 0.9, respectively. Moreover, the fuel properties of the oil were assessed and matched with the ASTM values of diesel, gasoline and kerosene oil. The oil was found to have a close resemblance to the commercial fuel. Therefore, it was concluded that utilizing florisil as the catalyst for the decomposition of waste polypropylene not only lowered the activation energy of the pyrolysis reaction but also upgraded the quantity and quality of the oil.

Development of the electrochemical, spectroscopic and molecular docking approaches toward the investigation of interaction between DNA and anti-leukemic drug azacytidine.

This study examines the interaction between pyrimidine nucleoside analogue azacytidine, an anti-leukemic drug, and DNA by employing electrochemical, UV-vis spectroscopy, fluorescence spectroscopy and molecular docking techniques. In the electrochemical technique, azacytidine and dsDNA interaction was investigated in two different ways: (1) in solution and (2) with a biosensor using differential pulse voltammetry (DPV) at a glassy carbon electrode. The interaction between azacytidine and dsDNA at increasing interaction times was investigated in line with the changes in adenine and guanine oxidation signals. In addition, interaction studies of polyguanine-azacytidine and polyadenine-azacytidine were performed with DPV. The binding constant values were calculated as 2.420 × 104 M-1 and 3.266 × 104 M-1 at 25 °C using UV and fluorescence spectroscopy, respectively. In conclusion, based on electrochemical and spectroscopic methods as well as molecular docking studies, it was predicted that azacytidine can bind to dsDNA via groove binding.

Oxide Derived Copper for Electrochemical Reduction of CO2 to C2+ Products.

The electrochemical reduction of carbon dioxide (CO2) on copper electrode derived from cupric oxide (CuO), named oxide derived copper (ODCu), was studied thoroughly in the potential range of -1.0 V to -1.5 V versus RHE. The CuO nanoparticles were prepared by the hydrothermal method. The ODCu electrode was used for carbon dioxide reduction and the results revealed that this electrode is highly selective for C2+ products with enhanced current density at significantly less overpotential. This catalyst shifts the selectivity towards C2+ products with the highest Faradaic efficiency up to 58% at -0.95 V. In addition, C2 product formation at the lowest onset potential of -0.1 V is achieved with the proposed catalyst. X-ray diffraction and scanning electron microscopy revealed the reduction of CuO to Cu (111) nanoparticles during the CO2 RR. The intrinsic property of the synthesized catalyst and its surface reduction are suggested to induce sites or edges for facilitating the dimerization and coupling of intermediates to ethanol and ethylene.