Influence Of Zro2 on The Physicochemical Properties of Phosphate-Based Glasses and Glass Ceramics

Abstract

Phosphate-based bioactive glasses and their glass ceramics for 47P₂O₅– (30.5)CaO–(22.5 ? x)Na₂O–xZrO₂ for different ZrO₂ contents (x = 0, 1.5, 3.0, 4.5, and 6.0 mol%) were prepared through melt quenching and controlled heat treatment procedures. The amorphous nature of glasses and the presence of crystalline phases in glass ceramics were studied by means of X-ray diffraction (XRD) studies. The density, molar volume, ultrasonic velocities, attenuation, elastic constants, and microhardness of glass and glass ceramics were used to study the structural changes. The formation of hydroxyapatite layer on the surface of glasses and glass ceramics after immersion in simulated body fluid (SBF) was explored through XRD, Fourier transform infrared (FTIR), and scanning electron microscopy (SEM) analyses. The results indicate that the added ZrO₂ increases the crosslink density of glasses, resulting in network stability, and also induces the formation of an apatite layer on the surface of glasses.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.     

Triazine interlinked covalent organic polymer as an efficient anti-bacterial agent

Herein, we report the synthesis of new covalent organic polymer comprising triazine and o-tolidine by solvothermal method. The formation of polymer was confirmed by Fourier transform infra red spectroscopy (FT-IR), cross polarization–magic angle spinning nuclear magnetic resonance (NMR), transmission electron microscopy, and scanning electron microscopy. Their antibacterial activity toward S. aureus (gram-positive) and P. aeruginosa (gram-negative) was assessed by the optical density measurements and direct contact method. These results have great significance toward the design of new porous polymers for antibacterial applications.     

Physicochemical properties of new cellulosic Artisdita hystrix leaf fiber

The characterization of new natural fiber is increasing due to its excellent properties. This drives investigators to create high performance composites. The present investigation was designed to study the physicochemical properties of fibers obtained from the leaf of the Artistida hystrix. The Artistida hystrix fibers (AHFs) had crystallinity index (44.85%), cellulose (59.54 wt%), hemicellulose (11.35 wt%), lignin (8.42 wt%), and density (540 kg m^?3). The tensile strength of AHFs was 440 ± 13.4 MPa with an average strain rate of 1.57 ± 0.04%. The calculated microfibril angle of AHFs was 12.64 ± 0.45°, which influenced the mechanical properties.     

Zinc-cobalt alloy: electrodeposition and characterization

Zinc-cobalt alloy electrodeposits offer enhanced corrosion protection to steel, compared to zinc deposits. A near neutral zinc-cobalt alloy sulfate bath was developed. In the absence of β-naphthol and sodium lauryl sulfate (SLS), only a light grey and non-uniform deposit was obtained. Addition of boric acid yielded a grey and uniform deposit. To obtain the grey uniform alloy deposit, the optimum bath composition was: 0.5 M ZnSO₄, 0.5 M CoSO₄, 40 g/L H₃BO₃, 0.865 g/L SLS and 0.345 g/L β-naphthol. The current efficiency for alloy deposition was 50% in the current density range 0.5–2.5 A/dm². X-ray fluorescence studies on the alloy deposit formed on steel revealed 58–75% zinc on the surface. Anodic stripping voltammetric studies were carried out on zinc-cobalt alloy films formed on glassy carbon to identify the phases formed in the alloy. Zn-Co alloy film dissolution peaks suggested the existence of β, β₁ and γ phases of the alloy. Electronic Publication     

An Overview of Metal-Organic Framework Based Electrocatalysts: Design and Synthesis for Electrochemical Hydrogen Evolution,Oxygen Evolution,and Carbon Dioxide Reduction Reactions

Due to the increasing global energy demands, scarce fossil fuel supplies, and environmental issues, the pursued goals of energy technologies are being sustainable, more efficient, accessible, and produce near zero greenhouse gas emissions. Electrochemical water splitting is considered as a highly viable and eco-friendly energy technology. Further, electrochemical carbon dioxide (CO₂) reduction reaction (CO₂RR) is a cleaner strategy for CO₂ utilization and conversion to stable energy (fuels). One of the critical issues in these cleaner technologies is the development of efficient and economical electrocatalyst. Among various materials, metal-organic frameworks (MOFs) are becoming increasingly popular because of their structural tunability, such as pre- and post- synthetic modifications, flexibility in ligand design and its functional groups, and incorporation of different metal nodes, that allows for the design of suitable MOFs with desired quality required for each process. In this review, the design of MOF was discussed for specific process together with different synthetic methods and their effects on the MOF properties. The MOFs as electrocatalysts were highlighted with their performances from the aspects of hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and electrochemical CO₂RR. Finally, the challenges and opportunities in this field are discussed.     

Synthesis and characterization of cobalt(II), nickel(II), copper(II) and zinc(II) complexes of 2-nitrobenzoic acid with methyl carbazate as ancillary ligand. Crystal structure of the copper(II) complex

Divalent metal complexes of general formula [M(2-nb)₂(mc)₂].2(2-nbH), where M = Co(II), Ni(II), Cu(II) or Zn(II), 2-nbH = 2-nitrobenzoic acid and mc = methyl carbazate (NH₂NHCOOCH₃), have been prepared and characterized by physicochemical and spectroscopic methods. Single-crystal X-ray study of the Cu(II) complex revealed that the molecule is centrosymmetric, with two N,O-chelating mc ligands in equatorial positions and a pair of monodentate 2-nb anions in the axial positions. The lattice 2-nbH molecules help to establish the packing of monomers through hydrogen-bonding interactions. Thermal stability and reactivity of the complexes were studied by TG–DTA. Emission studies show that these complexes are fluorescent.     

Tilianin: A Potential Natural Lead Molecule for New Drug Design and Development for the Treatment of Cardiovascular Disorders

Cardiovascular disorders (CVDs) are the leading risk factor for death worldwide, and research into the processes and treatment regimens has received a lot of attention. Tilianin is a flavonoid glycoside that can be found in a wide range of medicinal plants and is most commonly obtained from Dracocephalum moldavica. Due to its extensive range of biological actions, it has become a well-known molecule in recent years. In particular, numerous studies have shown that tilianin has cardioprotective properties against CVDs. Hence, this review summarises tilianin’s preclinical research in CVDs, as well as its mechanism of action and opportunities in future drug development. The physicochemical and drug-likeness properties, as well as the toxicity profile, were also highlighted. Tilianin can be a natural lead molecule in the therapy of CVDs such as coronary heart disease, angina pectoris, hypertension, and myocardial ischemia, according to scientific evidence. Free radical scavenging, inflammation control, mitochondrial function regulation, and related signalling pathways are all thought to play a role in tilianin’s cardioprotective actions. Finally, we discuss tilianin-derived compounds, as well as the limitations and opportunities of using tilianin as a lead molecule in drug development for CVDs. Overall, the scientific evidence presented in this review supports that tilianin and its derivatives could be used as a lead molecule in CVD drug development initiatives.     

Preparation and characterization of biodegradable sugarcane bagasse nano reinforcement for polymer composites using ball milling operation

The present work includes the processing and characterization of nano-based natural reinforcement for polymer composite materials. Sugarcane bagasse has been collected and the fibers were extracted using manual striping process. Undesirable materials present in the extracted fibers were removed by 1% NaOH-based chemical treatment. The macrofibers were reduced to nano scale by using high-energy ball milling process. Nanoparticles from bagasse fibers were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The degree of crystallinity of nano bagasse is 55.2% and it was reported by using XRD. A FTIR spectrum confirms the presence of cellulose functional groups in nano bagasse. The nano bagasse dimensions and morphology were investigated using SEM. The average length and diameter of the nano bagasse is 51.2 and 46.1 nm, respectively. Thermal stability of the nano bagasse was revealed by TGA analysis. The chemical composition of cellulose, lignin, and hemicellulose contents was also investigated.     

Quantum chemical calculation,topological analysis,biological evaluation and molecular docking of allo-ocimenol against breast cancer

The main aim of this study is to identify the structural stability of allo-ocimenol and its molecular reactivity against breast cancer-associated proteins to confirm its anti-cancer capability using density function theory and molecular docking analysis. The structural optimization was carried out via the DFT/B3LYP technique with a 6-311++G (d,p) basis set. The molecular geometry and vibrational assignments of the Allo-Ocimenol molecule were analyzed through density functional theory (DFT). Through optimized molecular structure, the vibrational frequencies (FT-IR and FT-Raman) were assigned and related with experimentally observed vibrational frequencies and the UV spectrum was computed and experimentally confirmed. The allo-ocimenol's reactive activity was further analyzed through a computed molecular electrostatic potential surface. Utilizing the HOMO-LUMO energies and molecular electrostatic potential energy gap, the reactivity and molecular stability of the allo-ocimenol molecule was calculated. Mulliken and natural population analyses were used to determine the charge distribution across the allo-ocimenol atoms. The natural bond orbitals were used to demonstrate the bioactivity of the titled molecule. RDG evaluation was used to examine the weak interactions of the allo-ocimenol molecule. ELF and LOL analyses were utilized to investigate the topology of the allo-ocimenol molecule. Thermodynamic evaluation has been utilized to acquire values and asses the thermodynamic parameters that reveal the thermal stability of the title molecule. Allo-Ocimenol's anti-microbial activity was assessed through an in-vitro disc diffusion method, and its tumor inhibitory and pharmacokinetic properties were evaluated through an in-silico approach using molecular docking and ADMET investigation. Zones of clearance were seen in anti-microbial analyses at various concentrations, and the breast cancer target protein NAMPT established the greatest binding potential, with a docking value of −7.4 Kcal mol⁻¹.     

Reactions of co-ordinated ligands: Kinetics and mechanisms in the charge transfer interaction between dichloro or diaquo triethylene tetramine Co(III) and ferrocyanide

The cherry red-coloured solid state product obtained by the reaction ofcis-σ diaquo Co (III) triethylene tetramine with ferrocyanide was examined by thermogravimetric, infrared and M?ssbauer techniques. Its electronic spectrum in aqueous medium was interpreted to consist of charge transfer IT transition at 440 nm and a ligand field transition around 330 nm. The kinetics of formation of this 1:1 product in solution was also studied.