Chain flexibility versus molecular entanglement response to rubbing deformation in designing poly(oxadiazole-naphthylimide)s as liquid crystal orientation layers

Four poly(oxadiazole-imide)s containing naphthalene rings, with different flexibility and molecular weight, are investigated with respect to their rheological properties to establish the optimal processing conditions from solution phase to film state for liquid crystal orientation purposes. The film uniformity and strength are determined by monitoring the flow behavior and chain entanglements. The solution rheological data are in agreement with film tensile testing, revealing that higher molecular weight favors chain entanglements and implicitly the film mechanical resistance. In order to analyze the suitability of these films as alignment layers their surface is patterned by rubbing with two types of velvet. Liquid crystal alignment of 4′-pentyl-4-biphenylcarbonitrile nematic is tested by polarized light microscopy. The resulting behavior is correlated with the polyimide malleability and characteristics of the textile fibers, namely their polarity, size, and mechanical features. The competitive effects between chain flexibility and entanglements, together with the interactions occurring between the polymer and velvet are analyzed in order to explain the surface regularity, which influences the uniformity of the liquid crystal alignment. The contrast between dark and bright states recorded on the liquid crystal cell indicates that some of these polynaphthalimides are promising candidates for liquid crystal display devices.     

Processing and properties of a new biodegradable Mg−Zn−Ca−Zr alloy

Magnesium alloys are used for degradable orthopaedic and cardiovascular implants due to their favourable mechanical and biological properties, degradation ability in physiological environment and stimulatory effect on the new bone formation. The research challenges are related to the increase of biological and mechanical compatibility. For the present study, a magnesium based alloy design was conducted to the following chemical composition: Mg?2.7Zn?1Ca?0.6Zr (wt.%). A complex thermomechanical processing route was applied: a plastic deformation by extrusion at various temperatures and deformation degrees (400 °C–480 °C, ? = 20 %–40 %), followed by various final heat treatments at 200 °C–400 °C for 10 min–60 min. Further, the influence of processing parameters upon the structure, mechanical properties and biological response was studied. Processed specimens were characterized by scanning electron microscopy (secondary electron imaging and energy dispersive spectroscopy) and mechanically by tensile tests. The most representative results were obtained for the samples extruded at 450 °C/? = 20 %, followed by a final heat treatment at 350 °C/15 min, air cooling. Further, for samples which revealed promising results, in‐vitro testing was developed. Biocompatibility testing of the Mg?2.7Zn?1Ca?0.6Zr (wt.%) alloy was realized by indirect contact studies using the Vero (ATCC® CCL‐81?, American Type Culture Collection) cell line. Cells morphologies, cell viability and proliferation were evaluated.     

Study of electronic transport properties of some new N-(p-R-phenacyl)-1,7-phenanthrolinium bromides in thin films

The electrical conductivity (σ) and thermoelectric power (S) of six newly synthesized high resistivity organic salts, N-(p-R-phenacyl)-1,7-phenanthrolinium bromides (T compounds), were investigated as a function of temperature.     

Studies on physico-chemical and antibacterial properties of grafted pullulans solutions

The physico-chemical properties of three grafted pullulans (P) having linked poly(3-acrylamidopropyl)trimethylammonium chloride (pAPTAC) as side chains (P-g-pAPTAC1, P-g-pAPTAC2 and P-g-pAPTAC3 with 22.53, 29.05, and 34.51 (wt.%) of pAPTAC content in polymer, respectively) and possessing polyelectrolyte character were determined by light scattering analysis. All grafted pullulan aqueous solutions were tested in the presence of 0.5 M NaCl, KCl, NaNO₃ or KNO₃. The biggest associations were recorded in 0.5 M NaCl aqueous solutions for P-g-pAPTAC1, P-g-pAPTAC2 and P-g-pAPTAC3 according to the maximum values for R_g extracted from MALLS (multiangle laser light scattering) measurements. Also, the dominant conformation in salted solution of these polyelectrolytes was random coil as Debye plot analysis revealed. Antibacterial activity was tested by Kirby–Bauer diffusion method and all grafted pullulans dissolved in aqueous solutions of 0.5 M NaCl have developed inhibition zone against Staphylococcus aureus (ATCC 25923).     

Newly synthesized fused heterocyclic compounds in thin films with semiconductor properties

Temperature-dependent electrical conductivity and thermoelectric power of some recently synthesized fused heterocyclic compounds (nonsymmetrical bisindolizines), are studied. Thin-film samples (d = 0.10–0.20 μm) deposited from dichloromethane solutions onto glass substrates were used. Organic films with reproducible electronic transport properties can be obtained if, after deposition, they are submitted to a heat treatment within temperature range 300–600 K.The studied compounds show typical p-type semiconductor behavior. The activation energy of the electrical conduction ranges between 0.90 and 1.17 eV, while the ratio of charge carrier mobilities was found in the range 0.94–0.97.Some correlations between semiconducting parameters and molecular structure of the organic compounds have been discussed.In the higher temperature range (373–601 K), the electronic transport in examined compounds can be interpreted in terms of the band gap representation model, while in the lower temperature range, the Mott's variable-range hopping conduction model was found to be appropriate.     

Towards understanding of the photosensitive properties in lead-vanadate-tellurate unconventional glasses

This paper describes photosensitive properties and spectroscopic studies on the xPbO(100 − x)[6TeO₂·4V₂O₅] (where x = 0-100 mol%) glass system. Our FTIR, UV-vis spectroscopic data and density measurements exhibit compositional dependent trends and the existence of characteristic vanadate (orthovanadate, pyrovanadate) structural units in these glasses. By laser exposures of the samples, variations observed in the FTIR and UV-vis spectra show that the existence a redox couple between lead ions and vanadate network.     

Inulin mixed esters crosslinked with 2-ethyl-hexyl-acrylate and their promotion as bio-based materials

New inulin-based materials were obtained by graft-copolymerization of inulin (poly-β(1 → 2)-fructoside) with 2-ethyl-hexyl acrylate. Inulin mixed esters were first synthesized by acylation using methacryloyl and palmitoyl chlorides. Further, these esters were copolymerized with 2-ethyl-hexyl acrylate in order to obtain bio-based crosslinked materials that could be used as commodity plastics and that would have biodegradable properties. The obtained products were characterized using FT-IR and ¹H NMR spectroscopies, thermogravimetry; differential scanning calorimetry, and activation energy for the degradation processes (using Kissinger method) was calculated. These biomaterials were also subjected to density measurement, tensile and torsion tests to evaluate their mechanical properties.     

Organosoluble asymmetric aromatic polyamides bearing pendent phenoxy groups

This study focuses on the synthesis and characterization of new polyamides based on an aromatic asymmetric diamine‐containing phenoxy‐substituted benzophenone segment. Low‐temperature solution polycondensation reactions of this diamine with various aromatic diacid chlorides containing ether, hexafluoroisopropylidene or diphenylsilane groups resulted in polyamides with molecular weights in the range 102 900–113 200 g mol^?1. The structures of these monomers and the corresponding polymers were fully confirmed using elemental analysis and infrared and NMR spectroscopy. All polyamides were easily soluble at room temperature in polar aprotic solvents and even in less polar solvents such as tetrahydrofuran. The polymers showed excellent thermal stability, up to 385 °C, and displayed glass transition temperatures in the range 225–256 °C. All the polymers presented blue florescence upon irradiation with UV light and thus show promise for applications in electroluminescent devices. Copyright © 2011 Society of Chemical Industry     

Structural investigation of xFe2O3 · (100 − x)[P2O5 · TeO2] glass system by FT-IR study and EPR spectroscopy

Glasses from xFe₂O₃ · (100 − x)[P₂O₅ · TeO₂] system, with 0 ≤ x ≤ 50 mol%, were investigated by X-ray diffraction, FT-IR and EPR spectroscopies. The XRD patterns show a vitreous state of studied samples for x ≤ 35 mol% Fe₂O₃. The FT-IR spectrum of the P₂O₅ · TeO₂ glass matrix reveals a structure formed from PO₄, TeO₄ and TeO₃ units. The addition and the increasing of Fe₂O₃ content modify progressively the structure of the glass matrix. The local structure in the investigated glasses was revealed by means of EPR using Fe³⁺ (3d⁵; ⁶S_5/2) ions as paramagnetic probes. The EPR spectra present two resonance absorption lines characteristic to Fe³⁺ ions centred at g_eff ≈ 2.0, for 0.5 ≤ x ≤ 35 mol% and g_eff ≈ 4.3, for 0.5 ≤ x ≤ 5 mol%. The variation of the EPR parameters, the intensity and line-width of these absorption lines, with iron ions composition has been followed.