Rapid and Efficient Microwave‐Assisted Synthesis of Some New Triazol‐3‐one Derivatives

A growing body of literature has shown the effectiveness of using microwaves in chemical reactions. The aim of this study is to demonstrate a rapid and highly efficient synthesis of some new triazol‐3‐ones via microwave heating using a monomode microwave. Compared with the thermal process, the microwave heating induces a dramatic reduction of the reaction time and improvement of the yields. In this study, rapid N‐benzylation and N‐acetylation of triazol‐3‐ones were achieved by microwave irradiation method for the first time. The newly synthesized compounds showed moderate antimicrobial activity against the standard bacterial and fungal organisms tested.     

Photophysical,Electrochemical, Thermal and Morphological Properties of Polyurethanes Containing Azomethine Bonding

In this paper, three new low band gap Schiff bases were prepared by using 3-etoxy-4-hydroxybenzaldehyde and different o-phylene diamines. Then, these Schiff bases were converted to low band gap polyurethane derivatives, and their photophysical, electrochemical, thermal, mechanical and morphological properties were investigated. Photophysical properties of the compounds were investigated by using UV-Vis and photoluminescence (PL) spectroscopy. Electrochemical properties of Schiff bases and polyurethanes containing azomethine were investigated by using cyclic voltammetry (CV). Thermal decomposition and transitions were determined by using TG-DTA, DMA and DSC techniques, respectively. Morphological properties of the compounds were also determined by using scanning electron microscopy (SEM). SEM images showed that polyurethanes containing azomethine consist of semi-crystalline particles.     

Simulation of crystallization evolution of polyoxymethylene during microinjection molding cycle

A mathematical model coupled with a numerical investigation of the evolving material properties due to thermal and flow effects and in particular the evolution of the crystallinity during the full microinjection molding cycle of poly (oxymethylene) POM is presented using a multi‐scale approach. A parametric analysis is performed, including all the steps of the process using an asymmetrical stepped contracting part. The velocity and temperature fields are discussed. A parabolic distribution of the velocity across the part thickness, and a temperature rise in the thin zone toward the wall have been obtained. It is attributed to the viscous energy dissipation during the filling phase, but also to the involved characteristic times for the thermal behavior of the material. Depending on the molding conditions and the locations within the micro‐part, different evolution of crystallization rates are obtained leading to at least three to five morphological layers, obtained in the same part configuration of a previously work, allowing a clear understanding of the process‐material interaction.     

Biodegradable and antibacterial poly(azomethine‐urethane)‐chitosan hydrogels for potential drug delivery application

In this study, biodegradable and antibacterial poly(azomethine‐urethane) (PAMU)‐ and chitosan (CS)‐based hydrogels have been prepared for controlled drug delivery applications. Structural and morphological characterizations of the hydrogels were performed via Fourier transform‐infrared and scanning electron microscopy analyses. Thermal stability, hydrophilicity, swelling, mechanical, biodegradation, protein absorption properties, and drug delivery application of PAMU‐ and CS‐based hydrogels were also investigated. The swelling performance of the hydrogels was studied in acidic, neutral, and alkaline media. Swelling results showed that the hydrogels have higher swelling capacity in acidic and alkaline media than neutral medium. Biodegradation experiments of the hydrogels were also studied via hydrolytic and enzymatic experiments. The drug release property of the hydrogel was carried out using 5‐fluoro uracil (5‐FU), and 5‐FU release capacity of the hydrogels was found in the range from 40.10% to 58.40% after 3 days.     

Electrochemical Investigation of Metal-Free and Nickel-Containing Porphyrazines Carrying Eight Tosylaminoethylthia Groups

 In this study, the electrochemical properties of metal-free and nickel-containing porphyrazines with eight tosylaminoethylthia groups were investigated using cyclic voltammetry, double potential step chronoamperometry, double potential step chronocoulometry, and controlled potential coulometry. Cyclic voltammetry measurements showed that both compounds exhibit two quasi-reversible and an irreversible reduction waves. The first electron transfer reaction was followed by an irreversible chemical reaction, the second one by a reversible chemical reaction for both species. The electrode processes of metal-free and nickel-containing porphyrazines are diffusion controlled, but the double potential step chronocoulometry measurements indicated that the nickel porphyrazine is adsorbed at the electrode. However, a small adsorption current has no significant effect on the mass transport mechanism of the system. Diffusion coefficients of both compounds were determined by both cyclic voltammetric and chronocoulometric measurements. The diffusion coefficients of the reduced forms of the porphyrazines were found to be smaller than those of the neutral forms.     

New Energetic Copper(II) Complexes With Pyrazolyl Type Ligands

Nine Cu^II complexes ( I – IX ) containing the azide ion and bis‐2,6‐(pyrazol‐1‐yl)pyridine (pp), bis‐2,6‐(pyrazol‐1‐yl)pyridine (dmpp), and 2‐(pyrazol‐1‐yl)‐6‐(3,5‐dimethylpyrazol‐1‐yl)pyridine (mpp), which are derivatives of pyrazolylpyridine, were prepared in nonaqueous medium. These complexes were characterized by elemental analyses and IR spectroscopy. Crystals of one of these complexes [CumppClN₃ ( VII )] were prepared in suitable size, and a molecular structure of this complex was obtained with X‐ray diffraction method. Complexes were examined by thermogravimetry and differential scanning calorimetry methods. Thermal decomposition was observed in complexes including two azide groups similar to that seen in explosives. In the complexes containing one azide group, formation of the Cu^I complexes was observed after thermal decomposition of the azide group.     

Thermally degradable thermosetting materials

Thermosetting materials have been widely used in a variety of applications but they generally display poor tractability after curing, which limits their use in applications where degradable or re-workable polymers are advantageous. Moreover, recyclability and biodegradability of thermosetting polymer also limit their use in applications where recycling and biodegradation are important. A variety of thermally degradable linkages within thermosetting materials have been studied both in academia and industry to develop re-workable adhesives. This review reports the recent development in thermosetting materials containing thermally breakable linkages that exhibit re-workability as well as potential for recyclability and biodegradability.     

Optimization of a quarter-car suspension model coupled with the driver biomechanical effects

In this paper a Human-Vehicle-Road (HVR) model, comprising a quarter-car and a biomechanical representation of the driver, is employed for the analysis. Differential equations are provided to describe the motions of various masses under the influence of a harmonic road excitation. These equations are, subsequently, solved to obtain a closed form mathematical expression for the steady-state vertical acceleration measurable at the vehicle-human interface. The solution makes it possible to find optimal parameters for the vehicle suspension system with respect to a specified ride comfort level. The quantitative definition given in the ISO 2631 standard for the ride comfort level is adopted in this paper for the optimization procedure. Numerical examples, based on actually measured road profiles, are presented to prove the validity of the proposed approach and its suitability for the problem at hand.     

Line-laser-based yarn shadow sensing break sensor

In this paper, a line-laser-based yarn break sensor is proposed. In the proposed sensor, yarns are illuminated by a line laser placed on one side of the yarn plane. A screen is placed on the other side and the image formed on the screen is detected by a camera. The total number of yarns is compared with the total number of shadows formed by the yarns or the total number of light spots formed due to the distances between yarns. If the total number of yarns to be detected is greater than the total number of shadows or light spots formed due to the distances between the yarns, the sensor warns of breaking. In the proposed method, evaluation is made using only light spots or shadows formed by the yarns. Consequently, the yarn type, structure, color, or dimensions do not affect the results.Design principles of the line-laser-based yarn break sensor, which consists of a screen and a Charged Coupled Device (CCD) camera, are presented. The screen displays the shadows formed by the yarns and the light spots formed due to the distances between them. The CCD camera detects the image on the screen. Formation of the shadows by the yarns is explained and an analytical formula that expresses the dimensions of the shadows is obtained. The detection area of the sensor is expressed relative to the total number of yarns, yarn thickness, and distances between the yarns. Line laser radiation angle and light spot intensity equations are obtained relative to the width of the detection area and the height of the line laser placement. The screen length is obtained relative to the number of yarns and the placement of the laser, the yarn plane, and the screen.Different placement situations of the line laser (transmitter), the screen, and the CCD camera (receiver) relative to the yarn plane are discussed. An experimental setup is developed to test the system. The image formed on the screen is studied.