Analysis of Physical and Thermodynamic Properties of Poly(2-Phenyl-1,3-Dioxolane-4-Yl-Methyl-Methacrylate-Co-Styrene) Polymer with Inverse Gas Chromatography

In this study, physical and thermodynamic properties of poly(2-phenyl-1,3-dioxolane-4-yl-methyl-methacrylate-co-styrene) (PDMMA-ST) were investigated by using inverse gas chromatography. Two groups of solvents with different chemical natures and polarities were used to obtain information about PDMMA-ST-solvent interactions: alcohols and alkanes. The specific retention volume (V_g ⁰), the sorption enthalpy (ΔH₁ ^S), sorption free energy (ΔG₁ ^S), sorption entropy (ΔS₁ ^S), the weight fraction activity coefficients of solute probes at infinite dilution (Ω ₁ ^∞), and Flory-Huggins interaction parameters (χ ₁₂ ^∞) between polymer and solvents were determined for the interactions of PDMMA-ST with alcohols and alkanes by inverse gas chromatography in the temperature range of 333–473 K. Also, the solubility parameters of PDMMA-ST at infinite dilution were found by plotting the graph of [(δ ₁ ²/RT) - χ ₁₂ ^∞/V₁] versus solubility parameters, δ ₁, of probes.     

Synthesis and characterization of novel poly(dimethylsiloxane)/polyindole composites

A series of composites of polyindole (PIN) and poly(dimethylsiloxane) (PDMS) were synthesized chemically using FeCl₃ as an oxidant agent in anhydrous media. The composites were characterized by FTIR and UV‐visible spectroscopies, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X‐ray diffraction (XRD), elemental analysis, inductively coupled plasma‐optic emission spectroscopy (ICP‐OES), magnetic susceptibility, stress–strain experiments, and conductivity measurements. The conductivities of PIN at different temperatures were also measured and it was revealed that their conductivities were slightly increased with increasing temperature. Moreover, the freestanding films of PDMS/PIN composites were prepared by casting on glass Petri dishes to examine their stress–strain properties. From thermogravimetric analysis results it was found that PDMS/PIN composites were thermally more stable than PIN. Thermal stabilities of PDMS/PIN composites increased with increasing PIN content. It was found that the conductivities of PDMS/PIN composites depend on the indole content in the composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

An investigation of some Schiff bases as corrosion inhibitors for austenitic chromium–nickel steel in H2SO4

The corrosion inhibition of austenitic chromium–nickel steel by two Schiff bases, N-(1-toluidine)salicylaldimine and N-(2-hydroxyphenyl)salicylaldimine, was investigated in sulphuric acid medium. The effect of concentration and temperature on inhibition properties was determined. It was found that when the concentrations of inhibitor were increased the inhibition efficiencies () and surface coverage () increased. Some thermodynamic parameters such as free energy of adsorption, G _ads, and enthalpy, H, were determined for the Schiff bases. Experimental results agree with the Temkin isotherm for N-(1-toluidine)salicylaldimine, but the Langmuir isotherm is more appropriate for N-(2-hydroxyphenyl)salicylaldimine.     

Comparison of melt extrusion and thermokinetic mixing methods in poly(ethylene terephthalate)/montmorillonite nanocomposites

The scope of this study consists in studying the effects of processing type on thermal stability of poly(ethylene terephthalate) (PET) and its nanocomposites prepared with organically modified clays. To achieve this goal, an intercalating agent was synthesized and montmorillonite type of clay modified with this intercalating agent was mixed with the PET by using melt extrusion and high‐shear thermokinetic mixing method. According to the results, manganese in the raw clay—though chemically bound—was found to be responsible for the decreased intrinsic viscosity (IV) values, i.e. decreased molecular weight in PET/organoclay nanocomposites. Besides, it was revealed that working on the thermokinetic mixer provided substantial contributions such as shorter processing times in comparison to the melt extrusion method, elimination of drying step before melt processing, which has been accepted as an inevitable process for PET so far, less thermal degradation because of short processing times, and more homogeneous and better dispersion of the clay particles in PET matrix phase. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Poly(azomethine-imide)s containing siloxane moities: Optical,thermal, mechanical,and morphological properties

A new series of poly(azomethine-imide)s having siloxane moities in backbone was prepared using different dianhydrides.Thermal, optical, and morphological properties of these polymers were clarified. Also, bulky  CO and  CF₃ group effects and meta or para-substituted aldeyhde effects on the mentioned properties were evaluated. The structural characterization of poly(azomethine-imide)s was carried out using a FT-IR spectroscopy. The optical properties of the polymers were performed via an UV–Vis spectrophotometer. Optical band gap of the poly(imide)s containing azomethine was calculated between 2.20 and 2.33 eV. Thermal behavior of poly(azomethine-imide)s was also studied using TG-DTA, DSC, and DMA techniques. The onset degradation temperature and percentage char values of the polyimides were found in the range from 429 to 545 °C and 22 to 35%, respectively. Thermal stability results demonstrated that benzophenone bearing poly(azomethine-imide)s have higher onset temperature, percentage char, and the glass transition temperature than poly(azomethine-imide)s derived from hexafluoroisopropylidene. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48364.     

Production of nano zinc borate (4ZnO·B2O3·H2O) and its effect on PVC

In this study, nano sized zinc borate powder with a formula of 4ZnO·B₂O₃·H₂O was synthesized using 2ZnO·3B₂O₃·3.0–3.5H₂O as a starting chemical which was produced using a wet chemical method. After dissolving 2ZnO·3B₂O₃·3.0–3.5H₂O in an ammonia solution, the clear solution was boiled until a white powder formed. The resultant powder was characterized with XRD, FTIR, TGA and TEM. XRD, FTIR and TGA results proved that the powder was belonged to the 4ZnO·B₂O₃·H₂O. Nano composites of 4ZnO·B₂O₃·H₂O–polyvinylchloride (PVC) were produced by injection moulding by adding 1 and 5 wt% zinc borate powders into PVC to enhance its flame retardancy. Limiting oxygen index (LOI) of virgin PVC increased from 41% to 47% and 54% for the 1 and 5 wt% zinc borate added PVC, respectively. Nano zinc borate addition into the PVC does not have considerable negative effect on the mechanical properties of zinc borate–PVC composites even at high amounts of 5 wt%.     

Properties of pumice aggregate concretes at elevated temperatures and comparison with ANN models

The mechanical properties and thermal conductivity of concretes including pumice aggregate (PA) exposed to elevated temperature were analyzed by thermal conductivity, compressive strength, flexure strength, dynamic elasticity modulus (DEM) and dry unit weight tests. PA concrete specimens were cast by replacing a varying part of the normal aggregate (0–2 mm) with the PA. All concrete samples were prepared and cured at 23 ± 10C lime saturated water for 28 days. Compressive strength of concretes including PA decreased that reductions were 14, 19, 25 and 34% for 25, 50, 75 and 100% PA, respectively. The maximum thermal conductivity of 1.9382 W/mK was observed with the control samples containing normal aggregate. The tests were carried out by subjecting the samples to a temperature of 0, 100, 200, 300, 400 500, 600 and 700 °C for 3 h, then cooling by air cooling or in water method. The results indicated that all concretes exposed to a temperature of 500 and 700 °C occurred a significant decrease in thermal conductivity, compressive strength, flexure strength and DEM. An artificial neural network (ANN) approach was used to model the thermal and mechanical properties of PA concretes. The predicted values of the ANN were in accordance with the experimental data. The results indicate that the model can predict the concrete properties after elevated temperatures with adequate accuracy. Copyright © 2016 John Wiley & Sons, Ltd.     

Photoluminescence characterization and heat treatment effect on luminescence behavior of BaTa2O6:Dy3+ phosphor

Undoped and Dy³⁺‐doped barium tantalate phosphors were synthesized by the solid‐state reaction method at 1425°C. Also, 10 mol% Dy³⁺‐doped BaTa₂O₆ was sintered between 1150 and 1425°C in order to determine temperature effect on structural and luminescence properties. Afterwards, they were characterized by XRD, SEM‐EDS and photoluminescence (PL) analyses. PL spectra exhibited the excitation peaks between 300 and 440 nm. Two typical emissions were observed at 486.2 nm (blue) and 577.7 nm (yellow) due to the ⁴F_9/2→⁶H_15/2 and ⁴F_9/2→⁶H_13/2 transitions, respectively. Emission intensities increased with increasing doping concentration of Dy³⁺ up to 10 mol% and then decreased due to the concentration quenching effect. Moreover, depending on the increase in heat treatment temperature, the intensity of emission reached maximum at 1425°C. The calculated CIE chromaticity coordinates of phosphors located in the white light region.     

Synthesis and characterization of imine‐coupled polyphenols containing carbazole units

Imine coupled phenolic monomers containing carbazole unit were synthesized in four steps. The monomers were polymerized via oxidative polycondensation by air as oxidant in an aqueous alkaline medium at 50°C. The structures of compounds were confirmed by ultraviolet–visible (UV–vis), Fourier transform infrared, and ¹H‐ and ¹³C‐NMR techniques. The conductivity measurements of these polymers were made by the four‐point probe technique and iodine was used as doping agent. The highest occupied molecular orbital, the lowest unoccupied molecular orbital, and electrochemical and optical band gap values were calculated by the results of the UV–vis and the cyclic voltammetry measurement, respectively. The number‐average molecular weight, weight‐average molecular weight, and polydispersity index values were determined by the size exclusion chromatography technique. Also, thermal behavior of these polymers was determined by thermogravimetric/differential thermal analysis measurements in a N₂ atmosphere between 20 and 1000°C. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009