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The study analyzed the structural characteristics of carbon nanomaterials obtained at different time parameters of the synthesis based on X-ray diffractometry, Raman spectroscopy, and scanning microscopy. According to the Raman spectroscopy and X-ray scattering data, the crystallite size of nanotubes is estimated to be in the range from 9 to 38 nm. With the synthesis time of 90 minutes, the nanotube crystallite size remains minimal in comparison with other samples, which is confirmed, among other things, by various diagnostic methods. Based on the X-ray diffraction data, the Lc and La crystallite sizes (longitudinal and perpendicular to the direction of the carbon layers) were calculated using the Selyakov-Scherrer formula. The sizes of nanotube crystallites as a result of increasing the synthesis time are in the range of 9-12 nm in the longitudinal direction and 22-38 nm in the perpendicular direction. The diffraction patterns of the samples do not reflect the presence of a significant amount of graphite; the intensity structure is predominantly in the (002) and (004) peaks, which are characteristic of nanotubes. As a result of the use of nanotubes as a modifier component with a synthesis duration from 40 to 90 minutes, an increase in the performance of the composite up to 20-25 % relative to the control sample is observed.

Clay minerals and sheet silicates are the main constituents of lutites and clays. These materials are relevant in earth science research as well as in economic geology because of the great variety of applications, based on their particular features at different levels of aggregation in mineral assemblages and on the microstructural and structural characteristics of the mineral constituents frequently characterized by micro- and nanocrystalline appearance. Thus, X-ray diffraction is a main tool for fundamental and applied research of these materials. The present review concerns their microstructural research from powder X-ray diffraction data.

This report investigates the effect of substrate and nitrogen (16 keV N+) ion implantation on the structural, morphological, compositional, and electrical properties of V2O5 thin films which are grown by thermal evaporation on various substrates, including glass, Si, and sapphire (termed V2O5:Gl, V2O5:Si, and V2O5:Sp, respectively). Structural analysis showed the formation of the mixed (α, and β-V2O5) phases on all substrates; however, the β-V2O5 phase is highly dominant in the V2O5:G and V2O5:Si samples. A deformation in the β-phase of V2O5 thin film under ion implantation-induced strain results in a change of crystallite size. Irradiation suppresses XRD peaks in relative intensities, indicating partial amorphization of the film with defect formation. Microstructural analysis confirmed the formation of uniform-sized nanorods for V2O5:Si, whereas isolated crystallites were formed for other types of substrates. Thermal conductivity may influence the size and shapes of V2O5 crystallite forms on different surfaces. Silicon absorbs heat more effectively than sapphire or glass, resulting in nanorod formation. A decrease in optical bandgap and electrical conduction has been observed due to increased oxygen vacancies, induced electron scattering, and trapping centres on N+ implantation. The present study thus offers the unique advantage of simultaneous reduction in optical band-gap and conductance of V2O5 thin films, which is important for optoelectronic applications.

MoO2 micro-powders with a mean pore size of 3.4 nm and specific surface area of 2.5 g/cm3 were compacted by dry pressing, then pressureless sintered at a temperature of 1000–1150 °C for 2 h or for a sintering time of 0.5–12 h at 1050 °C in an N2 atmosphere. Then, their microstructure evolution for morphology, crystallite, and grain growth were investigated. By sintering at a certain temperature and times, the irregular shape of the MoO2 powders transformed into an equiaxed structure, owing to the surface energy, which contributed to faster grain growth at the initial stage of sintering. The crystallite and grain sizes exponentially increased with the sintering time, and the growth exponent, n, was approximately 2.8 and 4, respectively. This indicates that the crystallite growth is governed by dislocation-mediated lattice diffusion, and the grain growth is determined by surface diffusion-controlled pore mobility. The increase in sintering temperature increased both crystallite and grain size, which obeyed the Arrhenius equation, and the activation energies were determined to be 95.65 and 76.95 kJmol−1 for crystallite and grain growths, respectively.

The stable EPR signal produced by ionizing radiation in crystalline D-mannose (C6H12O6) and separated from cranberries (Vaccinium oxycoccus) was studied. The isothermal heating of irradiated sample at 95°C for 10 minutes (melting point of D-mannose is 132°C) resulted in the modification and simplification of the EPR signal involved. The isotropic quartet has been recognized in the EPR signal of heat-treated sample. Molecular structure of the isotropic quartet identified in the complex EPR signal of D-mannose crystallite is proposed.

High-energy milling process on ceramic material was analyzed, it process generate modifications on morphology and particle size, the process showed the last one relation with the crystallite size, about of structural analysis Rietveld refinement let identify anisotropy with the variations on crystalline planes and deformations occasioned by milling process, the particle size decrease with the process, similar tendency was observed on the images obtained by Scanning Electronic Microscopy, an result in this study was the variation on magnetization without chemical reaction under non-stoichiometric conditions and the agglomerates sizes observed on samples it is by process.

The stable and complex EPR signals produced by the action of ionizing radiation on crystalline L-sorbose (C6H12O6) separated from rowan berries (Sorbus aucuparia) were studied. Isothermal heating of the samples at the temperature close to the melting point of L-sorbose (140°C) results in the modification and simplification of the EPR signal involved. In the EPR signal of heated L-sorbose, the isotropic quartet was distinguished. In the differential spectrum obtained by subtraction of normalized spectra of unheated and heated L-sorbose, the isotropic doublet was identified in addition. The DFT fitting offers the probable assignment of the EPR signals to specific radical structures.

Nowadays, improvement of the surface finish of parts manufactured by fused deposition modelling is a well-studied topic. Chemical post-treatments have proven to be the best technique in terms of time consumption and smoothness improvement. However, these treatments modify the structure of the material and, consequently, its mechanical properties. This relationship was studied in this work. In this case, on the basis of a previous study on crystallisation, polylactic acid pieces were subjected to different post-treatments to evaluate their effects on the sample’s mechanical properties, i.e., tensile strength and hardness. Models were obtained according to their percentage of crystallisation, which was related to the different treatments, as well as immersion time. Dramatic changes were obtained within a wide range of material behaviour with some treatments. Specifically, changes were obtained in the maximum stress (from 55 to 20 MPa), in elongation (from 3% to 260%), and in the hardness scale (Shore D to A).

In this study, TiO2⁻ZnFe2O4 (ZFO) core-shell nanorods with various ZFO crystallite thicknesses were synthesized through sputtering-deposited ZFO thin films onto the surfaces of TiO2 nanorods. By coupling the ZFO narrow bandgap oxide with TiO2, an enhanced photodegradation efficiency of methylene orange under irradiation was achieved. Structural analyses revealed that ZFO crystallites fully covered the surfaces of the TiO2 nanorods. The sputtering-deposited ZFO crystallites on the head region of the composite nanorods were markedly thicker than those covering the lateral region of the composite nanorods. The coverage of ZFO crystallites on the TiO2 nanorods led to an improved light harvesting, a decrease in the hole⁻electron recombination rate, as well as the enhanced photodegradation activity of the TiO2⁻ZFO heterostructures under irradiation. The optimized ZFO thickness on the head region of the composite nanorods was approximately 43 nm on average and that at the lateral region of the composite nanorods was 15 nm, which exhibited superior photodegradation ability to methylene orange and retained a stable photodegradation efficiency of approximately 97% after cycling tests. The results herein demonstrate that sputtering deposition of ZFO crystallite with tunable thickness is a promising approach to designing TiO2⁻ZFO composite nanorods with various ZFO coverage sizes and to adjust their photodegradation ability toward organic dyes.

In this work, untreated bovine cortical bones (BCBs) were exposed to a range of heat treatments in order to determine at which temperature the apatite develops an optimum morphology comprising porous nano hydroxyapatite (nanoHAp) crystals. Rectangular specimens (10 mm × 10 mm × 3–5 mm) of BCB were prepared, being excised in normal to longitudinal and transverse directions. Specimens were sintered at up to 900 °C under ambient pressure in order to produce apatites by two steps sintering. The samples were characterized by thermogravimetric analysis, X-ray diffraction (XRD), and scanning electron microscopy (SEM) attached to an energy-dispersive X-ray spectroscopy detector. For the first time, morphology of the HAp particles was predicted by XRD, and it was verified by SEM. The results show that an equiaxed polycrystalline HAp particle with uniform porosity was produced at 900 °C. It indicates that a porous nanoHAp achieved by sintering at 900 °C can be an ideal candidate as an in situ scaffold for load-bearing tissue applications.

Zirconia (ZrO2) nanopowder was synthesized using sucrose and fructose as a chelating agent from zirconium hydroxide. The synthesized powders were characterized by X-ray diffraction (XRD), simultaneously thermal analysis (STA), BET surface area, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The above-experimental results showed that the synthesized powders had particle sizes in the range 40-60 nm and mean crystallite sizes of 7-8 nm. Finally, in this research, chelating agents of sucrose and fructose were compared and the obtained results demonstrated that using fructose, nanopowder of zirconia with tetragonal phase was obtained.

The development of limes obtained by firing of a ground calcium carbonate (GCC) from Clariana (Tarragona), at constant maximum temperature (960 ºC) and at different permanence times was studied. Reflections 111, 200, 220, 311, corresponding to structural planes of higher morphological appearance (and, as a result, of slower cristallite growing rate), are analized using a single line simplified XRD method. Values of cristallite size obtained by this way are significative different for the different studied directions, and range from 334 Å to 3796 Å. The order of cristallite growing rates is 1 1 1 < 1 0 0 < 1 1 0 < 3 1 1 which agrees the order of morphological prevalence, according to the Donay & Harker’s law.Se estudia el desarrollo crstalino de CaO obtenido por calcinación (a temperatura máxima constante de 960ºC y distintos tiempos de permanencia) de un carbonato cálcico molido (CCM) proveniente de Clariana (Tarragona). Aplicando un método de análisis microestructural simplificado, de una sola línea, se analizan las reflexiones 111, 200, 220 y 311, asociadas a planos estructurales de mayor expresión morfológica y por ende de menor velocidad de crecimiento cristalino, obtienendose valores de tamaño de cristalito, con diferencias significativas para las distintas direcciones registradas y situados entre 334 y 3796 Å. El orden de las correspondientes velocidades de crecimiento de cristalito analizadas es 111 < 100 < 110 < 311, coincidente con el de preferencia morfológica establecida por la ley de Donay y Harker.

Spin-crossover (SCO) triazole-based coordination polymers can be synthesized by micelle techniques, which almost always lead to rod-shaped nanoparticles. In order to notably reach new morphologies, we explore here the potentiality of the spray-drying (SD) method to get SCO materials. Three SCO coordination polymers and a mononuclear complex are investigated. In all cases, the SD method obtains particles definitely showing SCO. The features of the latter are yet always different from those of the referenced materials, in the sense that SCO is more gradual and incomplete, in adequacy with the poor crystallinity of the powders obtained by SD. In the case of coordination polymers, the particles are preferentially spherical. Indications of possible polymorphism and/or new materials induced by the use of the SD method are evidenced. In the case of the mononuclear complex, the SD method has allowed reproducing, in a quick and easy way, the well-known bulk compound. This exploratory work demonstrates the relevance of the concept and opens the way to a systematic scrutiny of all the experimental parameters to tune the size, morphology, and properties of the SD-synthesized SCO particles.