Influence of TiN dopant on microstructure of TiB2 ceramic sintered by spark plasma

In this study, the impact of TiN as a sintering aid on the relative density and microstructure of TiB₂ ceramic was investigated. Monolithic TiB₂ and TiB₂ doped with 5?wt% TiN were sintered at 1900?°C for 7?min dwell time under the pressure of 40?MPa by spark plasma. The addition of TiN affected the microstructure of TiB₂-based sample considerably depicting the finer grains in the as-sintered ceramic. X-ray diffraction evaluation indicated that no interaction occurred between the initial materials. However, detail investigation by the map analysis and energy dispersive spectroscopy results revealed the formation of in-situ nano-sized hBN secondary phase in the TiN-doped TiB₂. In addition, TiN played a remarkable role on increasing the relative density of TiN-doped TiB₂ ceramic producing a nearly fully dense ceramic with relative density of 99.9% in comparison with the monolithic ceramic having 96.7% relative density.     

Spark plasma sintering of Al-doped ZrB2–SiC composite

This research presents the influence of Al addition on microstructure and mechanical behavior of ZrB₂–SiC ultra-high temperature ceramic matrix composite (UHTCMC) fabricated by spark plasma sintering (SPS). A 2.5?wt% Al-doped ZrB₂–20?vol% SiC UHTCMC was produced by SPS method at 1900?°C under a pressure of 40?MPa for 7?min. The microstructural and phase analysis of the composite showed that aluminum-containing compounds were formed in-situ during the SPS as a result of chemical reactions between Al and surface oxide films of the raw materials (i.e. ZrO₂ and SiO₂ on the surfaces of ZrB₂ and SiC particles, respectively). The Al dopant was completely consumed and converted to the intermetallic Al₃Zr and Al₄Si compounds as well as Al₂O₃ and Al₂SiO₅. A relative density of 99.8%, a hardness (HV5) of 21.5?GPa and a fracture toughness (indentation method) of 6.3?MPa?m^1/2 were estimated for the Al-doped ZrB₂–SiC composite. Crack bridging, branching, and deflection were identified as the main toughening mechanisms.     

Dendritic macromolecules containing several types of functional groups

Dendritic macromolecules containing several types of functional groups were successfully synthesized through divergent method. Poly(ethylene glycol) was functionalized using cyanuric chloride and it was reacted with p‐toluidine at room temperature and a macromolecule containing chloride and methyl functional groups (PEG‐Cl₂‐Me₂) was obtained. Substitution of chloride functional groups of PEG‐Cl₂‐Me₂ by hydroxyl functional groups led to a macromolecule containing methyl and hydroxyl functional groups (PEG‐Me₂‐OH₄). Hydroxyl functional groups of PEG‐Me₂‐OH₄ were reacted with cyanuric chloride and PEG‐Me₂‐Cl₈ was obtained. Finally, PEG‐Me₂‐Cl₈ was reacted with p‐aminophenol at room temperature and a macromolecule containing methyl, hydroxyl, and chloride functional groups (PEG‐Me₂‐(PhOH)₄‐Cl₄) was obtained. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

RNA secondary structured logic gates for profiling the microRNA cancer biomarkers

Deregulation of microRNAs expression is symptomatic of cancer disease and occurs before the awareness of cancer signs. Early detection of cancer disease can improve or drop the disease entirely. DNA computing is an emerging field of detecting microRNAs based on toehold‐mediated strand displacement reactions, which is a more efficient method than the commonly used method like real‐time PCR. Accuracy and cost of diagnostic applications are essential criteria that are achieved by using the DNA logic gates based on the DNA computing method. In this study, the authors proposed the multi‐input liver cancer biosensor with the RNA secondary structure motifs as the computational module and two approaches are suggested.Inspec keywords: cancer, biocomputing, biochemistry, DNA, RNA, biosensors, logic gates, liver, macromolecules, genetics, molecular biophysics, diseasesOther keywords: RNA secondary structured logic gates, microRNA cancer biomarkers, microRNAs expression, cancer disease, cancer signs, detecting microRNAs, toehold‐mediated strand displacement reactions, DNA logic gates, DNA computing method, multiinput liver cancer biosensor, RNA secondary structure motifs     

Densification improvement of spark plasma sintered TiB2-based composites with micron-, submicron- and nano-sized SiC particulates

Taguchi design of experiments methodology was used to determine the most influential spark plasma sintering (SPS) parameters on densification of TiB₂–SiC ceramic composites. In this case, four processing factors (SPS temperature, soaking time, applied external pressure and SiC particle size) at three levels were examined in order to acquire the optimum conditions. The statistical analysis identified the sintering temperature as the most effective factor influencing the relative density of TiB₂–SiC ceramics. A relative density of 99.5% was achieved at the optimal SPS conditions; i.e. temperature of 1800?°C, soaking time of 15?min and pressure of 30?MPa by adding 200-nm SiC particulates to the TiB₂ matrix. The experimental measurements and predicted values for the relative density of composite fabricated at the optimum SPS conditions and reinforced with the proper SiC particle size were almost similar. The mechanisms of sintering and densification of spark plasma sintered TiB₂–SiC composites were discussed in details.     

Coupled particle swarm optimization method with genetic algorithm for the static–dynamic performance of the magneto-electro-elastic nanosystem

As a first attempt, Fourier series expansion (FSE), particle swarm optimization (PSO), and genetic algorithm (GA) methods are coupled for analysis of the static–dynamic performance and propagated waves in the magneto-electro-elastic (MEE) nanoplate. The FSE method is presented for solving the motion equations of the MEE nanoplate. For increasing the performance of genetic algorithms for solving the problem, the particle swarm optimization technique is added as an operator of the GA. Accuracy, convergence, and applicability of the proposed mixed approach are shown in the results section. Also, we prove that for obtaining the convergence results of the PSO and GA, we should consider more than 16 iterations. Finally, it is shown that if designers consider the presented algorithm in their model, the results of phase velocity of the nanosystem will be increased by 27%. A useful suggestion is that there is a region the same as a trapezium in which there are no effects from magnetic and electric potential of the MEE face sheet on the phase velocity of the smart nanoplate, and the region will be bigger by increasing the wavenumber.

     

Investigating the effect of SPS‎ parameters on densification ‎and fracture toughness of ZrB2-SiC nanocomposite‎

In this study, the effect of sintering parameters on densification and fracture toughness of spark plasma sintering ZrB₂-SiC nanocomposites was evaluated. For this purpose, ZrB₂-??30?vol% SiC nanocomposites in the conditions of ?1600?°C-4?min, 1700?°C-4?min, 1800?°C-4?min, 1800?°C-8?min, 1800?°C-12?min? were sintered.? Scanning Electron Microscopy (SEM) was used in order to investigate the ?microstructural variations. The bulk density was measured accoring to ASTM C 373–88. Single edge notch beam (SENB) method was used to ?determine the fracture toughness of samples. Microstructural observations showed that ?an increase in sintering temperature led to slight ?increase in SiC grains size but no sensitive variation in ZrB₂. However, increasing the sintering time resulted to increase both ZrB₂ and SiC grain size. Also, it was found, temperature and time ascent always increases the relative density. In addition, it was concluded that optimal temperature and time to reach the highest fracture toughness are 1800?°C and 8?min, respectively. Investigation of SEM images of the Vickers indent and their path propagation showed that the deviation and branching of crack are the most important toughening ?mechanisms in ZrB₂-SiC nanocomposites.?     

Combined role of SiC whiskers and graphene nano-platelets on the microstructure of spark plasma sintered ZrB2 ceramics

This research explores the sintering behavior and microstructure of ZrB₂-based materials containing graphene nano-platelets (GNPs) and SiC whiskers (SiC_w). Spark plasma sintering (SPS) process at 1900 °C was implemented to sinter the specimen, leading to a composite with 100% relative density. High-resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), field emission-electron probe microanalyzer (FE-EPMA), and high-resolution X-ray diffractometry (HRXRD) were employed to study the SPSed sample, along with the thermodynamics predictions. According to the HRXRD result and microstructural observations, the sintering process was non-reactive, which was endorsed with the XPS analysis. Furthermore, graphene presented a beneficial role for eradicating the oxide impurities in the sample during the sintering. Such oxide impurities were reduced to the original phases of SiC and ZrB₂, contributing to porosity removal. Nanostructural investigations revealed the formation of ultrathin amorphous interfaces (~10 nm) between ZrB₂/graphene phases, disordered atomic planes in graphene platelets, and dislocations in ZrB₂ grains. One reason for generating crystalline defects in the microstructure was found out to be the mismatches amongst the elastic properties of the available compounds in the system.     

Synthesis and microstructural characterization of low to high molecular weight poly(vinylphosphonic acid)s: effect of molecular weight and temperature on acidity and polyelectrolyte behavior

Poly(vinylphosphonic acid) (PVPA) was synthesized by free radical polymerization of vinylphosphonic acid (VPA) in different solvents. Bromotrichloromethane as a chain transfer agent (CTA) was used in some experiments to control molecular weight of the PVPA. The effects of solvent type and initiator and CTA concentrations on the microstructure, molecular weight and stereoregularity of the resulting PVPA was extensively investigated by FTIR, ¹HNMR, ³¹PNMR and elemental analysis. Polymers with a number-average molecular weight (M_n) in the range of 1550 to 42,190 gmol^?1 were prepared. High molecular weight PVPA with M_n of 42,190 gmol^?1 was obtained from aqueous solution polymerization of VPA with initiator/monomer molar ratio of 0.16/100 at 80°C. Molecular weight decreased with increasing the concentration of initiator and CTA. ¹HNMR spectra were used to investigate tetrad sequences for the methylene protons of PVPA, from which stereochemical information of the polymer chain was obtained. Tetrad sequences were also calculated by Bernoullian probabilities. Moreover, the percent of head-to-head and tail-to-tail irregularities of the resulting PVPA were obtained to be in the range of 16.6–58% depending on the reaction conditions. The PVPA synthesized in acetic anhydride as a solvent had highest amount of the irregularities due to the high reaction rate, which does not allow controlling the structure. Furthermore, due to the importance of PVPA in the proton exchange membranes (PEMs), the effects of molecular weight and temperature on the acidity and titration behavior of PVPA polyelectrolyte were investigated. It was found that molecular weight has no significant effect on the acidity and dissociation of protons at operational conditions of degree of dissociation lower than 0.5. It was also found that by increasing the temperature, pH values were decreased, meaning that dissociation of protons and consequently the proton conductivity of PVPA membranes can be affected by temperature. Titration behavior of PVPA also showed that the PVPA has a behavior similar to a monoprotic acid.