Degradation of a polyester‐urethane coating: Physical properties

In this article we studied the evolution of thermomechanical properties of a polyester‐urethane coating during degradation under different degradation conditions, i.e., aerobic and anaerobic conditions with and without dry/wet cycling during degradation. Dynamic mechanical and thermal analyses show that under aerobic conditions the coatings become stiffer and more brittle in the glassy state. This stiffening is probably due to the increase in the amount of hydrogen bonding and the formation of oxidized groups which increase the polarity of the material and enhance the interactions of the polymer segments. However, oxidation reactions result in a considerable decrease in cross‐link density and stiffness in the rubbery state. Both changes, in the glassy and rubbery states, give rise to development of internal stresses. These stresses increase as the degradation process proceeds. Nevertheless, for samples exposed to anaerobic conditions, the stiffness remains constant in the glassy state and the cross‐link density slightly increases as a result of degradation. This reconfirms the dominance of the effect of oxidation reactions on the mechanical failure of the coatings. Oxygen permeation measurements show a more‐or‐less time‐independent diffusion coefficient and a gradual decrease in solubility of oxygen as a function of exposure time. This results in a slight decrease in oxygen permeation (mainly in the early stage of the degradation) as degradation proceeds. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 659–671     

Synthesis of thermally stable aromatic poly(spiroorthocarbonate)s having a Cardo or bent structure

Novel poly(spiroorthocarbonate)s [poly(SOC)]s having a Cardo or bent structure were synthesized by polycondensation of several bis‐catechols having fluorene (BCFL), spirobisindane (BCSPI), or spirobischromane (BCSPC) in the structure with 2,2,6,6‐tetrachlorobenzo[1,2‐d:4,5‐d’]bis[1,3]dioxole (4ClBD). Synthesis of poly(SOC)s was confirmed by NMR and IR spectrometry. The poly(SOC)s obtained from BCFL or BCSPC were soluble in common organic solvents. The glass transition temperature of the poly(SOC)s was not detected by differential scanning calorimetry (DSC) in the range of 50–300 °C. The 10 wt % decomposition temperature of the poly(SOC)s was found to be above 400 °C. These results indicated the high thermal stability of the poly(SOC)s. Soluble poly(SOC)s could be possessed to form a film on a glass plate by the spin coat method. The obtained polymer films were 0.2 μm in thickness with 95% light transmission in the optical wavelength range. These results suggested that the Cardo or bent structure may block the packing of the main‐chain of the structure, which improves the solubility of the polymers, increases transparency, and enhances the thermal stability of SOCs. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1409‐1416     

Application of acoustic methods for a non-destructive evaluation of the elastic properties of several typologies of materials

In solid phase materials, differently from what happens in the fluid phase, elastic waves propagate both through longitudinal and transverse waves. From the speed of propagation of longitudinal and transverse waves, it is possible to evaluate important elastic properties of the solids under study, namely the Young’s modulus, the Poisson’s coefficient, the bulk modulus and the shear modulus. This work suggests an accurate method for measuring wave propagation speeds in homogeneous and non-homogeneous materials with the purpose to evaluate their mechanical properties and the associated uncertainty.First of all, to assess the performance of the proposed methodology, based on the “pulse-echo” technique, in terms of accuracy and precision, measurements of wave propagation speeds have been carried out, in atmospheric conditions, in well-known homogeneous and isotropic materials, such as copper, aluminum, stainless steel and also polymethyl methacrylate (Plexiglas®), Teflon® and optical glass BK7. These results were compared with the values reported in literature (if present), showing how published speed of sound data are very disperse and not so reliable owing to the lack of a precise uncertainty evaluation and of the temperature value associated to the measurement. Then, the same experimental apparatus was used for measuring speed of sound as a function of temperature (from 274.15 to 313.15 K) for 304 stainless steel and oxygen free copper, showing a good accuracy of the results also for temperature conditions far from ambient. Finally, the same procedure was applied to a non-homogeneous solid, obtaining some very preliminary results in typical mediterranean building material, as Carrara marble.     

Blue TiO2 nanotube arrays as semimetallic materials with enhanced photoelectrochemical activity towards water splitting

In the past years there has been a great interest in self-doped TiO₂ nanotubes (blue TiO₂ nanotubes) compared to undoped ones owing to their high carrier density and conductivity. In this study, blue TiO₂ nanotubes are investigated as photoanode materials for photoelectrochemical water splitting. Blue TiO₂ nanotubes were fabricated with enhanced photoresponse behavior through electrochemical cathodic polarization on undoped and annealed TiO₂ nanotubes. The annealing temperature of undoped TiO₂ nanotubes was tuned before cathodic polarization, revealing that annealing at 500 °C improved the photoresponse of the nanotubes significantly. Further optimization of the blue TiO₂ nanotubes was achieved by adjusting the cathodic polarization parameters. Blue TiO₂ nanotubes obtained at the potential of –1.4 V (vs. SCE) with a duration of 10 min exhibited twice more photocurrent response (0.39 mA cm^-2) compared to the undoped TiO₂ nanotube arrays (0.19 mA cm^-2). Oxygen vacancies formed through the cathodic polarization decreased charge recombination and enhanced charge transfer rate; therefore, a high photoelectrochemical activity under visible light irradiation could be achieved.     

Effects of lanthanides doping on the optical properties of graphene/WSe2 heterostructure based on ab-initio calculations

Based on the density functional theory, we discussed the electronic and optical properties of graphene/ WSe₂ (GW) heterostructure after lanthanides doping. Red shift appears and the optical parameter values are improved in the low energy region after the lanthanides are doped. Different doping types are also discussed. In the case of single doping, substitute Yb atom on W site will improve the peak values of the optical parameters greatly. In the case of co-doping, it is found that the effect will be more obvious when the two doped lanthanide atoms are located in the second neighboring positons. These results suggest that lanthanides doping does adjust the electronic structure and improve the optical properties of GW heterostructures, which providing useful guidance for the design of novel optical nanodevices based on two-dimensional materials.     

Biobased vinyl levulinate as styrene replacement for unsaturated polyester resins

Vinyl levulinate (VL) is used as a biobased reactive diluent in styrene (St)‐free unsaturated polyester resins (UPR). The reactivity ratios for the radical copolymerization of VL with diethyl fumarate (DEF) are determined by the Jaacks method (r_VL = 0.01 and r_DEF = 0.81 at 60 °C in DMSO‐d₆). The properties of UPRs having a stoichiometric ratio between unsaturated groups from the UPR and either St or VL are compared. Defect‐free, slightly yellow, transparent, and rigid thermosets are obtained after a mild curing cycle. Due to unfavorable reactivity ratios about 5.5 wt % of unpolymerized VL remains inside the network and acts as plasticizer. Consequently, compared with St‐based ones, VL‐based UPRs exhibit lower α relaxation (T_α = 180 and 100 °C, respectively), lower elastic moduli at the rubbery plateau (G′ = 10⁸ and 10⁷ Pa) and lower mechanical properties as measured by three points bending tests. Strain at break (ε_f = 1.8 ± 0.2%) and Charpy impact strength (～2.7 ± 0.3 kJ m^?2) are comparable independently of the RD chemical nature. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3356–3364     

Thermo and mechanoluminescence studies of BZT phosphor

Mechanoluminescence (ML) and thermoluminescence (TL) in barium zirconium titanate (BZT) is reported for the first time. The BZT powder sample, belonging to perovskite category is synthesized using solid state reaction technique. The sample is prepared at a temperature of 1200 °C. The obtained specimen is thoroughly characterized paying particular attention to their structure, composition, morphology and optical properties. The surface morphology and structural properties are analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD patterns confirm the formation of crystalline perovskite type cubic structure. Also, highly agglomerated, porous and regular shaped particles are seen by SEM. The optical properties of as prepared sample is presented and discussed in terms of ML and TL. The ML intensity is found to be maximum for the sample irradiated for 10 min. More than one maxima in TL glow curve reveals that the traps are distributed in separate groups at different depths and corresponding values are calculated using initial rise method.     

Effect of tensile load on the actuation performance of pH‐sensitive hydrogels

pH‐responsive hydrogels are capable of converting chemical energy to mechanical work. To optimize their use as actuators, their response when operating against an external load must be fully characterized. Here, the actuation strain of a model pH‐sensitive hydrogel as a function of different constant loads is studied. The experimental actuation strain, produced by switching the pH from 2 to 12, decreases significantly and monotonically with increasing initial tensile load. Two models are developed to predict the actuation strain as a function of applied stress. Simple mechanical models based on the change in hydrogel modulus and cross sectional area due to the change in pH are unsatisfactory as they predict only a small change in actuation strain with increasing external stress. However, the model based on the elastic and mixing free energy functions derived from the Flory–Huggins theory is found to accurately account for the actuation strain as a function of stress. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 218–225