Behaviour of 54.4SiO2-13.7Na2O-1.7K2O-5.0CaO-12.4MgO-0.6Y2O3-11.3Al2O3-0.9B2O3 HT-SOFC glass sealant under oxidising and reducing atmospheres

The behaviour of the promising glass sealant 54.4SiO₂-13.7Na₂O-1.7K₂O-5.0CaO-12.4MgO-0.6Y₂O₃-11.3Al₂O₃-0.9B₂O₃ for solid oxide fuel cells (SOFCs) under SOFC operating conditions was studied. First, the kinetics of the crystallisation processes at the operating temperature (850 °C) was discussed (maximum exposure time of 1000 h), and the effect of crystallisation on the coefficient of thermal expansion (CTE) of the sealant was studied. Furthermore, the degradation processes at the interface of the glass sealant and functional SOFC materials (Crofer 22 APU, YSZ, and NiO(Ni)-YSZ) during exposure to 850 °C in oxidising and reducing atmospheres for 500 h were studied. The tests demonstrated good performance of the sealant studied and possibility of its application in SOFCs.     

Improved biogas yield from organic fraction of municipal solid waste as preliminary step for fuel cell technology and hydrogen generation

Biogas utilization in fuel cell technology and hydrogen generation is a modern and economically viable approach. A pretreatment step prior to anaerobic digestion (AD) is obligatory to increase the hydrolysis, solubilize the complex matter present in organic fraction of municipal solid waste (OFMSW) and to achieve higher yield of biogas. This study was intended to find out the effects of thermal, chemical and thermochemical pretreatments on the properties and structure of OFMSW and also on biogas production. There was an increase in chemical oxygen demand of 6.87, 1.61 and 11.60% for thermal, chemical and thermochemical pretreatments, respectively. Also, the content of volatile solids was reduced by 2.36% by thermochemical pretreatment. FTIR, XRD and SEM analysis revealed that these pretreatments also caused chemical and morphological changes on the substrate, as a result reduced its crystallinity and enhanced the rate of hydrolysis. A significant increase of 54% in biogas yield was achieved after thermochemical pretreatment in comparison to untreated OFMSW sample.     

Effect of sintering temperature on the morphology,crystallinity and mechanical properties of carbonated hydroxyapatite (CHA)

Effect of sintering temperature on the physical and mechanical properties of synthesized B-type carbonated hydroxyapatite (CHA) over a range of temperature in CO₂ atmosphere has been investigated. The B-type CHA in nano size was synthesized at room temperature by using a direct pouring wet chemical precipitation method. The synthesized CHA powders were subsequently consolidated by sintering treatment from 800 to 1100 °C. The sintered CHA samples were evaluated using X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectrometry, X-ray fluorescence (XRF), carbon-hydrogen-nitrogen-sulfur-oxygen (CHNS/O) elemental analyzer, Field emission scanning electron microscopy (FESEM), and Vicker's indentation technique. The results obtained from XRD and FESEM indicated that the synthesized B-type CHA powders were nanometer in size. The crystallinity and crystallite size of the sintered CHA samples were increased due to increasing sintering temperature. The heat treatment between 800 °C and 1000 °C has resulted in coarsening and increased hardness of the sintered CHA samples. However, these properties began to deteriorate when sintering beyond 1100 °C due the formation of calcium oxide.     

Vacancy-engineered V2O5-x films for ultrastable electrochromic applications

In the present study, we prepared vacancy-engineered V₂O_5-x films for electrochromic (EC) applications. To investigate the vacancy effect of V₂O_5-x films with high EC performance capabilities, precursor concentrations of V-based sol solutions were varied at 1 wt%, 5 wt%, and 10 wt%. Among them, V₂O_5-x films with a precursor concentration of 5 wt% (V₂O₅-5wt%) showed superior EC performance outcomes due to the (001)-plane-oriented crystal structure, which provides high electrical conductivity with the oxygen vacancy (V_o). In addition, the gravel-like uniform surface morphology with the optimized film thickness provides a stable electrochemical reaction during the EC measurement. As a result, V₂O₅-5wt% exhibited fast switching speeds (2.1 s for coloration and 3.6 s for bleaching), high transmittance modulation (ΔT) (51.32%), high coloration efficiency (CE) (52.3 cm²/C), and excellent cycle stability (85.85% ΔT retention after 500 cycles). In addition, V₂O₅-5wt% showed energy storage capability of 443.7 F/g at a current density of 2 A/g, thus proving its potential for use in multi-functional applications. Therefore, these results provide valuable insight related to the engineering of vacancies in EC films to achieve high-performance EC devices and additional multi-functional applications.     

Corrosion resistance and lifetime of polyimide-b-polyurea novel copolymer coatings

A novel class of polyurea-b-polyimide (PUI) block copolymer coating containing environmentally friendly aromatic polyurea has been successfully synthesized for corrosion protection of aluminum alloy 2024-T3 (Al 2024-T3). The PUI copolymer is able to self-assemble into a supramacromolecule by means of intra and inter-hydrogen bonds (H-bonds). The formation of H-bonds and effect of the later on the crystallinity of the copolymer was studied by using Fourier transform infrared spectroscopy (FTIR) and wide angle X-ray diffraction (WAXD). It was shown that increasing polyurea mole fraction up to 50 mol%, enhanced occurrence of H-bonding induced self-assembly, and resulted in remarkable enhancement in the degree of crystallinity, and corrosion resistance. Corrosion resistance and diffusivity of the copolymer coatings were investigated by electrochemical impedance spectroscopy (EIS), in a 3.5 wt% NaCl solution. The coating lifetime determined by using time-based corrosion resistance, was shown to be about 8 years for the optimized PUI copolymer coating. PUI coating synthesized by using 50 mol% of polyurea has a high contact angle (110°) and remarkably low surface energy of about 25.5 mJ/m².     

Evaluation of structural properties of AZO conductive films modification using low-temperature ultraviolet laser annealing

In this study, an ultraviolet (355 nm) laser processing system was developed to anneal aluminum-doped zinc oxide (AZO) thin films at room temperature in an air atmosphere; in this system, two key parameters, laser fluence and annealing speed, were varied. The structural properties of the films were thoroughly examined using field emission scanning electron microscopy, atomic force microscopy, and X-ray diffraction (XRD). The results showed that the laser fluence not only influenced the structural properties of the films, but also improved the crystallinity of the films after the laser annealing process, with minimal changes in the thickness of the films and the concentration of the elements in the films. The root mean square surface roughness (R_rms) of the films gradually increased as the laser fluence increased. Moreover, according to the XRD pattern of the films, the intensity of the main peak corresponding to the (002) direction increased as the laser fluence increased. The average crystallite size (20 nm) of the annealed films, determined using the Scherrer equation, was smaller than that of the as-deposited thin film (22 nm) due to the low temperature effect in the laser annealing process.     

Insights into the development of crystallinity in liquid urea-formaldehyde resins

Differently from most thermoset materials, urea-formaldehyde (UF) resins display the appearance of crystalline domains. In the effort of understanding the mechanism of formation of such crystals, wide angle X-ray diffraction (WAXD), infrared spectroscopy and transmission electron microscopy (TEM) were applied. Liquid UF resins with two different F/U mole ratios (i.e. 1.6 and 1.0) were investigated as a function of hardener level and curing times at room temperature. The WAXD results showed that the liquid UF resin with a low F/U mole ratio had a greater crystallinity than the one with a high F/U mole ratio. An advance in crystal formation in the low F/U mole UF resins was visible, especially in the first phases of curing. However, there were no significant differences in the degree of crystallinity as a function of hardener level. IR spectroscopy highlighted the important role of methylolated species in the formation of crystals. TEM results also confirmed the presence of crystals in all the considered liquid UF resins. The concentration of the hardener and the curing time were critical in shaping morphology and particle dispersion. As a function of the curing conditions, the globular structures present in the samples can aggregate into different morphologies, which can be fibrillar and also lamellar. The obtained results stress the importance of controlling the subtle interplay between crosslinking and formulation for the obtainment and control of the size, quantity and morphology of crystals in UF resins, and therefore for an effective tuning of their properties.     

Comparison of steam-alkali-chemical and microwave-alkali pretreatment for enhancing the enzymatic saccharification of oil palm trunk

This paper demonstrates two different pretreatment protocols for oil palm trunks (OPT); steam-alkali-chemical (SAC) and microwave-alkali (Mw-A) method. The composition, morphology, structure and crystallinity of OPT before and after pretreatment were analyzed. The effectiveness of the pretreated methods was investigated by performing enzymatic saccharification on the OPT. The physiochemical factors namely: enzyme ratio (cellulase to β-glucosidase), pH, temperature and substrate loading (w/v) on enzymatic saccharification were also investigated. The pre-determined optimal conditions were then used for further enzymatic hydrolysis of raw and pretreated OPT substrates. The results revealed a huge degree of reduction in lignin, up to 89% for SAC treated OPT and at least 15% for Mw-A treated OPT sample as compared to untreated ones. High glucose accumulation (79.4%) was obtained after 72 h saccharification for both pretreated OPT samples.     

The Effect of Drying Temperature on Physical Properties of Thin Gelatin Films

The molecular morphology of thin gelatin films, controlled through the casting temperature, was monitored by wide angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). Gelatin films dried at lower temperatures had a markedly higher crystalline or helical structure with a slightly higher T_g and lower ΔC_p compared with hot dried films, which had a more coiled structure. The relationship between molecular morphology and gelatin-water interaction in terms of hydration behavior and water diffusivity was assessed using dynamic vapor sorption (DVS). The sorption capacity increased and the level of hysteresis decreased with increasing the degree of crystallinity. The difference in the aging behavior of the films was explained in terms of the difference between the glass transition and aging temperatures, (Tg – Ta).     

Effects of second-phase particles and elemental distributions of ITO targets on the properties of deposited ITO films

As the key material of transparent electrodes in various optoelectronic devices, ITO targets with uniform microstructure and homogeneous elemental distributions are vital to obtain high-quality ITO films in industrial production. In this paper, the differences in the crystalline structure, sheet resistance and transmittance of ITO films with 40 nm, 70 nm and 100 nm thickness were studied between two ITO targets that were respectively sintered at 1580 °C for 10 h (target A) and 1600 °C for 5 h (target B). Surface morphology, surface roughness and thickness uniformity of ITO films with 100 nm thickness and etching property of ITO films with 40 nm and 70 nm thickness in mixed acids were further focused in the paper. The results indicate that target A, which owns homogeneous distributions of second-phase particles and elements, could be conductive to obtain the ITO films with low crystallinity that are easy to be etched leaving less and smaller residual particles. Based on the analysis, the change of sintering process has a great influence on the electrical and etching properties, but it has only a little influence on the optical property.