Functional Properties of Donor (Al) and Acceptor (Cu) Codoped High Dielectric Constant ZnO Nanoparticles

In this work, we have synthesized donor-acceptor (Al-Cu) codoped ZnO nanoparticles with a doping concentration of 0%, 0.25%, 0.5%, and 0.75% by coprecipitation method. The synthesized samples were then annealed at 350°C and 600°C. All the samples showed wurtzite structure of ZnO with no secondary phase. The increase in doping concentration led to deterioration of crystalline quality, while improved crystallinity was observed at higher annealing temperature. The morphological study of these samples showed good grain-to-grain contact with less isolated pores. These samples were further characterized by impedance spectroscopy for analyzing dielectric properties. The values of the real part of dielectric constant and tangent loss showed decreasing trend with frequency. The appearance of semicircular arcs in the impedance complex plane plots indicates contribution of grains and grain boundaries and presence of different relaxation processes. 0.5% Al and Cu codoped ZnO showed the best dielectric response with a high value of dielectric constant and low tangent loss.

Electrochemical Surface Biofunctionalization of Titanium through Growth of TiO2 Nanotubes and Deposition of Zn Doped Hydroxyapatite

The current research aim is to biofunctionalize pure titanium (Ti, grade IV) substrate with titania nanotubes and Zn doped hydroxyapatite-based coatings by applying a duplex electrochemical treatment, and to evaluate the influence of Zn content on the physico-chemical properties of hydroxyapatite (HAp). The obtained nanostructured surfaces were covered with HAp-based coatings doped with Zn in different concentrations by electrochemical deposition in pulsed galvanostatic mode. The obtained surfaces were characterized in terms of morphology, elemental and phasic composition, chemical bonds, roughness, and adhesion. The nanostructured surface consisted of titania nanotubes (NT), aligned, vertically oriented, and hollow, with an inner diameter of ~70 nm. X-Ray Diffraction (XRD) analysis showed that the nanostructured surface consists of an anatase phase and some rutile peaks as a secondary phase. The morphology of all coatings consisted of ribbon like-crystals, and by increasing the Zn content the coating became denser due to the decrement of the crystals’ dimensions. The elemental and phase compositions evidenced that HAp was successfully doped with Zn through the pulsed galvanostatic method on the Ti nanostructured surfaces. Fourier Transform Infrared spectroscopy (FTIR) and XRD analysis confirmed the presence of HAp in all coatings, while the adhesion test showed that the addition of a high quantity leads to some delamination. Based on the obtained results, it can be said that the addition of Zn enhances the properties of HAp, and through proper experimental design, the concentration of Zn can be modulated to achieve coatings with tunable features.

Improving the Performance of Mortars Made from Recycled Aggregates by the Addition of Zeolitised Cineritic Tuff

Metropolitan construction and demolition waste (CDW) is currently an important source of recycled materials that, despite having completed their useful life cycle, can be reincorporated into the circular economy process (CEP); however, the recycling process is very selective, and waste material is not always fully satisfactory due to the intrinsic nature of the waste. This work aims to demonstrate and establish how to increase the effectiveness of the construction and demolition waste in more resistant mortars, by mixing it with zeolitised cinerite tuff (ZCT) at varying normalised proportions. To attain the objectives of this research, a series of tests were done: First, a chemical, physical and mineralogical characterisation of the CDW and the ZCT through XRF, XRD, SEM and granulometric methods. Second, a technological test was made to determine the mechanical strength at 7, 28 and 90 days of specimens made with Portland cement (PC) and mixtures of PC/CDW, PC/ZCT, and PC/CDW-ZCT. The results obtained through the characterisation methods showed that the sample of construction and demolition waste consisted of the main phase made of portlandite and tobermorite, and by a secondary phase consisting of quartz, ettringite and calcite; whereas the ZCT has a main phase of mordenite and a secondary phase of smectite (montmorillonite), amorphous materials consisting of devitrified volcanic glass, quartz and plagioclase. Mechanical strength tests established that specimens made with PC/CDW mixtures have very discreet compressive strength values up to 44 MPa at 90 days, whereas specimens made with PC/ZCT mixtures achieved a remarkably high mechanical strength consisting of 68.5 MPa. However, the most interesting conclusion in this research is the good result obtained in mechanical strength of the specimens made up of mixtures of PC/CDW-ZCT, which increased from 52.5 to 62 MPa at 90 days of curing; this fact establishes the positive influence of ZCT on waste in the mortar mixtures, which permits the authors to establish that the objective of the work has been fulfilled. Finally, it can be argued that the results obtained in this research could contribute to more effective use of construction and demolition waste in metropolitan areas.

Structural and Transport Properties of La0.85Te0.15MnO3 Manganite and its Composite with Al2O3

The manganite systems investigated during the present work are pure La0.85Te0.15MnO3 (LTMO) and its composite with 12% concentration of Al2O3 nano powder (LTMO + Al2O3). The materials were prepared by the modified auto combustion technique. The samples were characterized by X-ray diffraction. The powder X-ray diffraction pattern of pure LTMO at room temperature shows that sample is in single phase with no detectable secondary phases and the sample have a rhombohedral structure in hexagonal with the space group R3c. The XRD pattern of LTMO + 12% Al2O3 indicates the clear presence of Al2O3 nano phase in the composite. In the present study, the FTIR Spectroscopy of both samples was carried out. It is clear from the Vibrational assignment for the value of corresponding peak position of FTIR spectra that no extra unwanted impurity is present in samples. A quantitative analysis of the energy dispersive spectroscopy (EDS) data indicates that the observed concentration of elements are very close to the calculated values from its chemical formula. R-T measurements reveals that the addition of secondary phase in manganite strongly influenced on electronic and magnetoresistance behaviour. We summarise some of the salient features of the results.

Spectroscopic evaluation of UVI–cement mineral interactions: ettringite and hydrotalcite

Portland cement based grouts used for radioactive waste immobilization contain high replacement levels of supplementary cementitious materials, including blast-furnace slag and fly ash. The minerals formed upon hydration of these cements may have capacity for binding actinide elements present in radioactive waste. In this work, the minerals ettringite (Ca6Al2(SO4)3(OH)12·26H2O) and hydrotalcite (Mg6Al2(OH)16CO3·4H2O) were selected to investigate the importance of minor cement hydrate phases in sequestering and immobilizing UVI from radioactive waste streams. U L III-edge X-ray absorption spectroscopy (XAS) was used to probe the UVI coordination environment in contact with these minerals. For the first time, solid-state 27Al magic angle spinning nuclear magnetic resonance (MAS-NMR) spectroscopy was applied to probe the Al coordination environment in these UVI-contacted minerals and make inferences on the UVI coordination, in conjunction with the X-ray spectroscopy analyses. The U L III-edge XAS analysis of the UVI-contacted ettringite phases found them to be similar (>∼70%) to the uranyl oxyhydroxides present in a mixed becquerelite/metaschoepite mineral. Fitting of the EXAFS region, in combination with 27Al NMR analysis, indicated that a disordered Ca- or Al-bearing UVI secondary phase also formed. For the UVI-contacted hydrotalcite phases, the XAS and 27Al NMR data were interpreted as being similar to uranyl carbonate, that was likely Mg-containing.

Effects of Cu substitution on microstructures and microwave dielectric properties of Li2ZnSiO4 ceramics

Herein, the influence of Cu2+ substitution on the phase composition, bulk density, microstructures, and microwave dielectric properties of Li2CuxZn1−xSiO4 (0 ≤ x ≤ 0.06) ceramics prepared by a solid-state reaction were investigated. The results of XRD and mapping showed that Cu2+ substitution can avoid the influence of secondary phase on the properties of samples. According to the analysis of bulk density, microstructure and microwave dielectric properties, a proper amount of Cu substitution not only improved the sintering characteristics of Li2CuxZn1−xSiO4 ceramics, reduced the densification temperature from 1250 °C to 950 °C, but also increased the Q×f value. Furthermore, Cu2+ substitution also improved the temperature stability of the samples. Particularly, the Li2Cu0.04Zn0.96SiO4 ceramics sintered at 950 °C for 5 h possessed excellent microwave dielectric properties: εr = 5.624, Q×f = 12,764 GHz, and τf = −77 ppm/°C, exhibiting a potential for the low temperature co-fired ceramic applications.

Flash Light Sintered Lanthanum Strontium Cobalt Ferrite(LSCF) Electrode for High Performance IT-SOFCs

The high temperature(900oC~) thermal sintering process is necessary to fabricate the Solid oxide fuel cells(SOFCs). However, the chemical reaction has occurred between solid oxide material components, electrode and electrolyte. In the case of lanthanum strontium cobalt ferrite (La0.6Sr0.4Co0.2Fe0.8O3-δ, LSCF) electrode, the SrZrO3(SZO) secondary phase is produced at the electrolyte interface even when using the gadolinium doped ceria(GDC) buffer layer for blocking the strontium and zirconium diffusion. The SZO layer hinders the oxygen ion transfer and deteriorates fuel cell performance. By using a novel flash light sintering(FLS) method, we have successfully solved the problem of secondary phase formation in the conventional high temperature thermal sintering process. The microstructure and thickness of the LSCF electrode are analyzed using a field emission scanning electron microscope(FE-SEM). The strontium diffusion and secondary phase are confirmed by X-ray diffraction (XRD), energy dispersive spectrometer method of SEM, TEM (SEM-, TEM-EDS). The NiO-YSZ anode supported LSCF cathode cells are adopted for electro chemical analysis which is measured at 750oC. The maximum power density of the thermal sintered LSCF cathode at 1050oC is 699.6mW/cm2, while that of the flash light sintered LSCF cathode is 711.6mW/cm2. This result proves that the electrode was successfully sintered without a secondary phase using flash light sintering.