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M. S. Boldin

Publications and source records attributed to M. S. Boldin.

9 recordsLinked to original sources

Effect of the parameters of bimodal microstructure on the mechanical properties of alumina: A case of sintering regime effects

The effect of sintering regimes on the density, microstructure parameters, and mechanical properties of Al2O3 and Al2O3 + 0.25%MgO ceramics has been investigated. The ceramics were sintered in three regimes: Regime I - heating at a constant rate (2.5, 5, 10, 20 C/min) up to the temperature T=1650C; Regime II - heating with a varied heating rate up to 1565C with the duration corresponding to sintering at the heating rate of 10 C/min in Regime I followed by a three-fold decrease in the shrinkage rate; Regime III - two-stage sintering: heating according to Regime II up to the temperature T1+1550C, then lowering the temperature down to T2 = 1300-1500C and holding for 3 h at the T2. The sintering regimes were chosen so that the ceramics had the relative density of 97-99% and a bimodal distribution of the microstructure parameters. The Al2O3 and Al2O3 + 0.25%MgO ceramics obtained in Regimes I-III had a microstructure with abnormally large grains in a fine-grained matrix. The sizes and volume fractions of the large grains depended on the sintering regime. Most abnormally large grains had elongated shapes that leads to deviations in the crack propagation trajectories from the straight line. The optimal parameters of the bimodal microstructure parameters distribution providing enhanced mechanical properties of the ceramics (hardness, indentation fracture toughness, ultimate strength) have been determined.

cond-mat.mtrl-sci

Low-temperature Spark Plasma Sintering of fine refractory composite powders core-shell: A case of the powders W@Ni

The mechanisms of fast low-temperature Spark Plasma Sintering (SPS) of W + 10% wt. Ni powders were investigated. The powder compositions were obtained in two methods: (i) by mixing W and Ni powders in a specified ratio (hereinafter referred to as W + Ni); (ii) by Ni deposition on the surface of submicron W particles allowing the formation of particles with a core W - shell Ni structure (hereinafter referred to as W@Ni). To reduce the concentrations of oxygen and oxides, the powders were annealed in hydrogen. The solid-phase sintering was performed at various temperatures (1000-1150°C), pressures (40-80 MPa), heating rates (50-500°C/min), and isothermal holding times (0-20 min). The sintering temperatures corresponded to the onset of intense dissolution of W in Ni. The samples had high relative density and small grain sizes. The activation energy of SPS of the mixed powders was close to the one of the grain boundary diffusion. The key mechanism for the compaction of W@Ni particles in the SPS process is Coble creep. The increasing of the sintering temperature was shown to lead to an increase in the solubility of W in Ni and, consequently, to an increase in the number of secondary Ni4W particles formed during cooling down. The grain growth has a minor effect on the mechanical properties of the W alloy compared to the changes in its phase composition.

cond-mat.mtrl-sci

Combined effect of SiC and carbon on sintering kinetics, microstructure and mechanical properties of fine-grained binderless tungsten carbide

The study investigates the density, phase composition, microstructure and mechanical properties (microhardness, fracture toughness) of binderless WC + SiC and WC + SiC + C ceramics obtained by Spark Plasma Sintering (SPS). Nanopowders of a-WC produced by DC arc plasma chemical synthesis were used as raw materials. Powder compositions for sintering contained graphite (0.3, 0.5% wt.) or b-SiC (1, 3, 5% wt.) with 0.3% wt. graphite. It was shown that WC + 1% wt. SiC + 0.3% wt.C ceramics have a homogeneous fine-grained microstructure, high relative density, increased microhardness and Palmquist fracture toughness (Indentation Fracture Resistance). The kinetics of the initial sintering stage of WC + C and WC + C + SiC powder compositions was also analyzed using high-temperature dilatometry at the conventional pressureless sintering (CPS) conditions. The CPS and SPS activation energies of WC + SiC powder at the intensive shrinkage stage were determined using the Young-Cutler model. The CPS activation energies of WC, WC + C and WC + C + SiC powder compositions are close to the activation energy of diffusion of the carbon C along the a-WC grain boundaries. The SPS activation energies of WC + C and WC+ C + SiC powder compositions turn out to be lower than the activation energy of the C of a-WC grain boundary.

cond-mat.mtrl-sci

Combined Thermal Expansion and Hydrolytic Stability Study of Lanthanide Vanadates LnVO4 and CaLnZr(VO4)3 (Ln = La, Nd, Sm, Eu, Gd, Dy, Yb) with Zircon and Monazite Structures

The paper presents the investigation of ordinary and ternary vanadates with zircon and monazite structures. Vanadates LnVO4 and CaLnZr(VO4)3 , where (Ln = La, Nd, Sm, Eu, Gd, Dy, Yb) and solid solution La0.3Nd0.5Sm0.1Eu0.1VO4, were prepared by precipitation reaction. Bulk ceramic samples were obtained from powders by Spark Plasma Sintering (SPS). The powders and ceramics were examined with several physicochemical methods. The coefficients of thermal expansion at 900°C were determined. The hydrolytic stability of ceramic materials was studied. The peculiarities of high-rate SPS of powders of ordinary and ternary vanadates were analyzed.

cond-mat.mtrl-sci

Low-temperature creep of binderless tungsten carbide with different grain sizes

The creep mechanism in the compression testing of the tungsten carbide with different grain sizes has been studied. The WC samples with high density (96.1-99.2%) were obtained by SPS from nano-, submicron, and micron-grade WC powders. The samples had a coarse-grained (CG) surface layers of ~0.3 mm in thickness and ultrafine-grained (UFG) central parts consisting of WC with a small fraction of W2C. The creep tests were conducted in two regimes: (Mode #1) holding at different temperatures (1300-1375C) at 70 MPa; (Mode #2) tests at different stresses (50, 70, 90 MPa) at 1325C. Tests in Mode #1 were done to determine the effective creep activation energy Qcr while tests in Mode #2 - to determine the coefficient n in the power law creep equation. The increasing of the fraction of the W2C particles from 1.7 up to 4% was found to result in a decrease in the Qcr from 17.5 down to 13 kTm. The coefficient n equals to 3.1-3.7. The Qcr in the WC sintered from nanopowders was shown to be 31 kTm. This value is 1.5-2 times greater than the Qcr in the UFG samples obtained by SPS from commercial powders. The increased fraction of the W2C formed when sintering the nanopowders with increased adsorbed oxygen concentration was suggested to be one of the origins of the increase in the Qcr when testing the UFG samples. The mechanical removing of the CG layers from the surfaces of the tungsten carbide sample was shown to result in an accelerated creep, insufficient decrease in the Qcr and coefficient n to 2.5-2.6. The creep rate of the samples was suggested to be determined simultaneously by the creep process in the CG surface layers and the creep process in the UFG central parts of the samples. The creep rate in the surface CG layers is determined by intensity of carbon diffusion in the WC crystal lattice while the creep rate in the UFG central parts - by the intensity of grain boundary diffusion.

cond-mat.mtrl-sci

Investigation of the microstructure of the fine-grained YPO$_4$:Gd ceramics with xenotime structure after Xe irradiation

The paper reports on the preparation of xenotime-structured ceramics by the Spark Plasma Sintering (SPS) method. Phosphates Y$_{0.95}$Gd$_{0.05}$PO$_4$ (YPO$_4$:Gd) were obtained by the sol-gel method. The synthesized nanopowders are collected in large agglomerates 10-50 mkm in size. Ceramics has a fine-grained microstructure and a high relative density (98.67%). The total time of the SPS process was approximately 18 min. High-density sintered ceramics YPO$_4$:Gd with a xenotime structure were irradiated with Xe$^{+26}$ ions (E = 167 MeV) to fluences of $1\times10^{12}$-$3\times 10^{13}$ cm$^{-2}$. Complete amorphization at maximum fluence was not achieved. As the fluence increases, an insignificant increase in the depth of the amorphous layer is observed. According to the results of grazing incidence XRD (GIXRD), with an increase in fluence from $1\times10^{12}$-$3\times 10^{13}$ cm$^{-2}$, an increase in the volume fraction of the amorphous structure from 20 to 70% is observed. The intensity of XRD peak 200 YPO$_4$:Gd after recovery annealing (700$^\circ$C, 18 h) reached a value of ~80% of the initial intensity I0.

cond-mat.mtrl-sci

Effect of grain boundary state and grain size on the microstructure and mechanical properties of alumina obtained by SPS: A case of the amorphous layer on particle surface

The effect of temperature modes and heating rates (Vh) on the shrinkage kinetics of submicron and fine aluminum oxide powders has been studied. The objects of research comprised (i) submicron alfa-Al2O3 powder, (ii) submicron alfa-Al2O3 powder with an amorphous layer on particle surface, (iii) fine alfa-Al2O3 powder. The alumina ceramic specimens were produced by Spark Plasma Sintering (SPS). Equally fine powders (i) and (ii) were used to analyze the effect of an amorphous layer on sintering kinetics. Powders (i) and (iii) were used to analyze the effect of the initial particle size on shrinkage kinetics. Shrinkage curves were analyzed using the Young-Cutler and Coble models. It has been shown that sintering kinetics is determined by the intensity of grain boundary diffusion for submicron powders and by simultaneous lattice and grain boundary diffusion for fine powders. It has been determined that an amorphous layer on the surface of submicron alfa-Al2O3 powder affects grain boundary migration rate and the Coble equation parameters at SPS final stages. It has been suggested that abnormal characteristics of the alumina ceramics sintered from a submicron powder with an amorphous layer on the particle surface are associated with an increased concentration of defects at grain boundaries that were formed during crystallization of the amorphous layer.

cond-mat.mtrl-sci

Synthesis and study of (Na, Zr) and (Ca, Zr) phosphate-molybdates and phosphate-tungstates: Thermal expansion behavior, radiation test and hydrolytic stability

Thermal expansion behavior at high temperatures of synthesized Na$_{1-x}$Zr$_2$(PO$_4$)$_{3-x}$(XO$_4$)$_x$, and Ca$_{1-x}$Zr$_2$(PO$_4$)$_{3-x}$(XO$_4$)$_x$, X = Mo, W compounds has been investigated. Ceramics with relatively high density (more than 97.5%) were produced by Spark Plasma Sintering (SPS) of submicron powders obtained by sol-gel synthesis. The study of strength characteristics has revealed that hardness the ceramics are greater than 5 GPa, and minimum fracture toughness factor was 1 MPa*m$^{1/2}$. It was found that ceramics have a high hydrolytic resistance in the static regime -- the minimum leaching rates for the Mo- and W-containing specimens were $31\times10^{-6}$ and $3.36\times 10^{-6}$ g/(cm$^2$*day), respectively. The ceramics had a high resistance to the irradiation by Xe$^{+26}$ multiple-charged ions with the energy 167 MeV up to the fluences in the range 1*10$^{12}$ - 6*10$^{13}$ cm$^{-2}$. The Mo-containing Na$_{0.5}$Zr$_2$(PO$_4$)$_{2.5}$(XO$_4$)$_{0.5}$ ceramics were shown to have a higher radiation resistance that the phosphate-tungstates.

cond-mat.mtrl-sci

Immobilization of the rare earth fraction in lanthanide phosphates LnPO4. Radiation and hydrolytic resistance of the matrix

Radiation and hydrolytic resistance of Eu0.054Gd0.014Y0.05La0.111Ce0.2515Pr0.094Nd0.3665Sm0.059PO4 with monazite structure has been studied. The powders were obtained by deposition from solutions. Ceramic specimens with relative density ~97% were obtained by Spark Plasma Sintering (heating rate Vh = 50 °C/min, sintering temperature Ts = 1070 °C, sintering time ts = 18 min). Irradiation by accelerated electrons up to dose of 10^9 Ge was found not to result in a destruction of the target phase. After the irradiation, an increasing of the leaching rate by an order of magnitude (up to ~10^{-8} g/(cm2*day)) and a reduction of the mechanical properties by 32% as compared to the non-irradiated ceramic specimen were observed.

cond-mat.mtrl-sci