Development of very high strength Mo2NiB2 complex boride base hard alloy

A previous investigation revealed that additions of Cr and V to the Mo₂NiB₂ complex boride base hard alloy changed the boride phase crystal structure from orthorhombic to tetragonal and resulted in a remarkable improvement of mechanical properties associated with microstructural refinement. Moreover, an addition of Mn turned out to be effective in further improvement of the mechanical properties in the V-containing alloy. In this investigation, Ni-5B-xMo-12.5V-2.5Mn (mass%) model alloys with four levels of Mo contents corresponding to Mo/B atomic ratio ranging from 1.0 to 1.3 were prepared to study the effect of the Mo/B atomic ratio on the mechanical properties and microstructure. The results indicated that transverses rupture strength (TRS) increased with increasing Mo/B atomic ratio and showed a maximum value of 3.2 GPa at Mo/B=1.2 and then decreased with increasing atomic ratio. Hardness increased linearly from 86.8 HRA to 90.8 HRA with increasing Mo/B atomic ratio.     

Portraits of some representatives of metal boride carbide and boride silicide compounds

Different ternary alkaline-earth and rare-earth metal boron carbide and silicide compounds are examined using the solid-state language of Zintl-Klemm concept, band structures, and density of states, in order to show that the topology of the non-metal sub-lattice is highly dependent on the electron count. It is also shown that the chemistry of rare-earth metal-boron-silicon does not parallel that of rare-earth metal-boron-carbon. B-C bonds are easily formed in the latter, leading to a large variety of different structural arrangements, whereas Si-B bonds are hardly observed in the former, except in insertion compounds.     

Mixed-ligand ternary complexes of potentially pentadentate but functionally tridentate Schiff base chelates

The potentially pentadentate chelate 2,6-diacetylpyridine-bis(N-methyl-S-methyldithiocarbazate) (Nmedapsme) has been synthesized and structurally characterized by X-ray diffraction. Its reactions with nickel(II) salts did not lead to pentadentate coordinated ligand complexes but ternary complexes of general formula, [Ni(Nmedapsme)(nmesme)L]X·H₂O (L = Br⁻, I⁻; X = I⁻, BF₄⁻) where Nmedapsme binds as a tridentate and nmesme = N-methyl-S-methyldithiocarbazate. The related ternary nickel(II) complexes of formula, Ni(Nmedapsme)(nmetsc)Br₂ has also been prepared and characterized. X-ray crystal structures of [Ni(Nmedapsme)(nmesme)I]I·H₂O and [Ni(Nmedapsme)(nmesme)Br]BF₄·H₂O revealed that, in these complexes, the Nmedapsme ligand acts as a tridentate NNN donor while the distal S-donors are not coordinated. The bidentate (NS) ligand, nmesme coordinates to the nickel(II) ion via the amino nitrogen and the thione sulfur atoms, the sixth coordination site is occupied by an anion. In both complexes, the nickel(II) ion adopts a distorted octahedral configuration. The complex [Cu(nmesme)₂(ONO₂)]NO₃ was obtained from an unsuccessful attempt to complex copper(II) with Nmedapsme. Hydrolysis of the parent Schiff base Nmedapsme occurred during complexation. An X-ray crystallographic structure analysis shows that the complex, [Cu(nmesme)₂(ONO₂)]NO₃ has an approximately square-pyramidal geometry with the two nmesme ligands coordinated to the copper(II) ion as NS bidentate chelating agents via the amino nitrogen and thione sulfur atoms and the fifth coordination position of copper(II) is occupied by a monodentate nitrate ligand.     

Synthesis and crystal structure of MgB12Si2—The first ternary compound in the system B/Mg/Si

We report on the synthesis of MgB₁₂Si₂ the first ternary compound in the system B/Mg/Si. Yellow transparent single crystals were yielded from the elements at 1600 °C in h-BN crucibles welded in Ta ampoules. MgB₁₂Si₂ crystallizes orthorhombic in the space group Pnma with , , and Z=4. The crystal structure is characterized by layers of B₁₂ icosahedra, connected by isolated Si atoms to a three-dimensional framework. Mg atoms are placed in voids of the framework. Each icosahedron forms 8 B-Si bonds and 4 exohedral B-B bonds. The Si atoms are tetrahedrally coordinated by B atoms of the B₁₂ icosahedra.     

Ecofriendly new nanocomposites coating formulation of zinc reinforced with calcium oxide nanoparticles synthesis from oyster shell

The zinc coating of mild undergoes rapid corrosion for a short period of time in harsh environments. This affects the durable life and overall performance of the zinc coatings. The electrochemical, oxidation, and wear performance, as well as the surface morphological properties of new nanocomposites coating formulations of zinc reinforced with calcium oxide nanoparticles, were studied in order to improve the corrosion and wear performance of zinc coatings. A current density of 1.5–2.0 A/cm² was used for the electrodeposition. The wear, oxidation, hardness, corrosion rate, and morphological properties were evaluated. The characterization of these composite coatings showed low wear rates and higher corrosion and oxidation resistance. At 1.5A/cm² current density, a 65.53% enhancement in the hardness values and 57.14% oxidation protection were obtained. The smaller crystallite size of the deposited sample is the main reason for the lower corrosion and wear resistance and higher hardness values obtained. It was established that waste oyster can be used for the electrodeposition of mild steel to enhance corrosion resistance and hardness values. CaOnp made from oyster shells has been shown to make mild steel more resistant to corrosion, wear, and oxidation.     

Synthesis and characterization of novel ternary deep eutectic solvents简

A series of room-temperature ternary deep eutectic solvents(TDESs) were prepared from imidazolium halides, zinc halides and amides. The [BMIM]Cl–ZnCl2 –acetamide(1:1:1) system shows the lowest freezing point( 60 8C) and lowest density in the series. The viscosity and conductivity of TDESs have an exponential relationship with temperature and can be fitted by Arrhenius equation.     

Frontal photopolymerization synthesis of multilayer hydrogels with high mechanical strength

Multilayer hydrogels were prepared by frontal photopolymerization of acrylamide and 2-acrylamido-2-methylpropane sulfonic acid using hydrophilic reactive microgels (HRM) as crosslinkers instead of conventional crosslinkers. The hydrophilic microgels (HM) were prepared by inverse emulsion photopolymerization and then were chemical modified by N-methylolacrylamide (NMA) to obtain HRM with CC double bonds. The HM and HRM was characterized by dynamic light scattering measurements, SEM, TEM and FTIR, respectively. It was found that the resulting multilayer hydrogels showed high fracture strength and high tensile elongation along parallel direction. However their fracture strength and tensile elongation along perpendicular direction was very weak. The swollen multilayer hydrogels were about 1.0–2.0 mm in thickness, the maximal equilibrium swelling degree was only 30.45. The multilayer hydrogels were characterized by DSC, TEM and XRD, respectively. The swelling property and mechanical strength of some typical multilayer hydrogels were studied.     

Development and thermal behaviour of ternary PLA matrix composites

Biodegradable PLA composites were prepared using microcrystalline cellulose (MCC) and silver (Ag) nanoparticles. The main objective of the present study is to develop new biopolymer composites with good mechanical properties, thermal stability, maintaining the optical transparency and also providing antimicrobial properties through silver nanoparticle introduction. Composites were prepared with 1%wt of Ag nanoparticles and 5%wt of MCC using a twin-screw microextruder; film parameters were optimized in order to obtain a thickness range between 20 and 60 μm.PLA composites maintained optical transparency properties of the matrix, while MCC was able to reduce polymer permeability. Thermal analysis revealed that MCC increased PLA crystallinity and the mechanical properties of the composites demonstrated that tensile modulus was improved by microcrystalline cellulose.     

Effect of montmorillonite on structure and properties of nanocomposite with PA6/PS/elastomer matrix

Polyamide nanocomposites with fair balance of mechanical properties were recently obtained by addition of finely dispersed clay-compatibilized rubber or rigid PS phase. This work deals with combination of both components, which recently led also to enhanced mechanical behaviour in an analogous reactively compatibilized ternary system.Application of clay to PA6/PS/EPR matrix leads to a decrease in particle size analogously to corresponding binary blends, but the effect of clay on toughness is predominantly contradictory, i.e., a decrease with increasing clay content was found. Also the toughening effect of formed core-shell (elastomer/clay) particles is lower in comparison with binary PA6/EPR. At the same time, in contrast to the PA/PS system, the presence of core-shell particles formed by PS/C15 preblending leads to fair mechanical behaviour including enhanced toughness. This documents a complex affecting of the system behaviour by clay and the expected synergistic cooperation of numerous clay-induced changes in both component parameters and structure. The obtained results indicate that a proper combination of rigid and elastomeric inclusions can lead to nanocomposites with balanced and enhanced mechanical behaviour.     

Spectral and thermal study of the ternary complexes of nickel with sulfasalazine and some amino acids

The ternary complexes of Ni(II) with sulfasalazine (H(3)SS) as a primary ligand and alanine (ala), aspartic acid (asp), histidene (hist), methionine (meth) and serine (ser) amino acids as secondary ligands have been synthesized. Characterization of the complexes was based on elemental analyses, IR, UV-vis, mass spectra, magnetic moment and thermal analysis (TG). The isolated complexes were found to have the general formula [M(HSS)(AA)]4H(2)O (AA=ala, asp, hist, meth, or ser amino acid) where nickel is tetra-coordinated. The thermal stability of the complexes was studied and the weight losses for the decomposition of the complexes were calculated and correlated with the mass fragmentation pattern. In most cases, the amino acid moiety is removed along with the Schiff base moiety leaving NiO as a metallic residue. The metallic residue was confirmed by powder XRD measurements.     

Fabrication of exfoliated graphite nanoplatelets-reinforced aluminum composites and evaluating their mechanical properties and corrosion behavior

Aluminum composites with different amounts of exfoliated graphite nanoplatelets particles were fabricated by powder metallurgy method. The mixture powders were consolidated at 520 MPa for 5 min and followed by pressureless sintering at 600 °C for 6 h. The mechanical properties of composites were evaluated by compression and hardness tests. The corrosion behavior in 3.5% NaCl solution was investigated using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) measurements. The mechanical testing results showed that the maximum strength and Vickers hardness increase as a function of exfoliated graphite nanoplatelets content. Corrosion data indicated that the presence of exfoliated graphite nanoplatelets and the increase of its concentration raise the corrosion rate and reduce the polarization resistance of Al. SEM/EDX investigations revealed that the presence of exfoliated graphite nanoplatelets activates the corrosion of Al due to the occurrence of galvanic corrosion. SEM/EDX investigations confirmed the electrochemical measurements showing that the increase of exfoliated graphite nanoplatelets content increases the corrosion of Al.     

Mechanical properties and frictional resistance of Al composites reinforced with Ti_3C_2T_x MXene

Two-dimensional(2D) Ti_3C_2T_x MXene is an attractive additive not only used in base oil due to its low friction coefficient,but also used in composites due to its high aspect ratio and rich surface functional groups.So far there has been intense research into polymer matrix composites reinforced with Ti_3C_2T_x,Here we report on the use of 2D Ti_3C_2T_x to enhance the mechanical and frictional properties of Al matrix composites.Ti_3C_2T_x/Al composites were designed and prepared by pre s sureless sintering followed by hot extrusion technique.The prepared composites exhibit a homogeneous distribution of Ti_3C_2T_x.The Vickers hardness and the tensile strength continuously increase with increasing Ti_3C_2T_x content.A hardness of 0.52 GPa and a tensile strength of 148 MPa were achieved in the 3 wt% Ti_3C_2T_x/Al composite.The frictional properties of pure Al and the Ti_3C_2T_x/Al composite were comparably studied under dry sliding.A low friction coefficient of 0.2,twice lower than that of pure Al,was achieved in the 3 wt%Ti_3C_2T_x/Al composite.Ti_3C_2T_x acting as a solid lubricant reduces the abrasive wear in the composite,improving the frictional properties of Al matrix composites.     

Structures and Properties of Cast Irons Reinforced by Trace Addition of Modified SiC Nanopowders

"To improve the performance of traditional cast iron, trance amount of surface modified nanometer SiC powders were added into the melted iron. The microstructures, the mechanical properties, as well as the wear resistance were investigated. The trace addition of SiC nano-powders were active due to the presence of structural defects arising from the treatment, they were eoient in affecting not only the generation and growth of crystals but also change the morphology of graphite. On the other hand, the addition of SiC nanopowders as heterogeneous seedings in the crystallization of liquid metals lead to the changing of supercooling temperature, so the ratio of ferrite and pearlite was changed. The mechanical characteristics and wear resistance were enhanced as a result of the improved graphite shape and changed matrix composition caused by the trace addition of SiC nanopowders (in amounts of about 0.01% mass). The strengthening mechanism and the free gap between powders were also discussed. It is suggested that the tensile strength, toughness, as well as the wear resistance can be improved simultaneously, which indicates the novel strengthening technology by trace addition of nanopowders is promising to extend to large-scale industrial production."     

Effect of sintering temperature on mechanical and microstructural properties of bovine hydroxyapatite (BHA)

The influence of sintering temperature on densification, microstructure and the mechanical properties of bovine hydroxyapatite (BHA), produced by a calcination method, was investigated. Densification and mechanical properties improved with increasing sintering temperature in the range between 1000°C and 1300°C, with optimum properties being obtained at a sintering temperature of 1200°C. The measured mechanical properties indicate that sintered BHA bodies are interesting biomaterials for further investigation in biomedical applications.     

稀土对TiC基金属陶瓷耐磨堆焊材料组织性能的影响

应用扫描电镜、透射电镜等测试手段和冲击试验,磨损试验,研究了TiC基金属陶瓷堆焊材料中加入稀土氧化物,对堆焊材料的组织,界面相结合,显微硬度,冲击韧性和磨损性能的影响,初步探讨了稀土氧化物改善界面显微结构,提高的胎体金属韧性的作用机制,研究结果表明,稀土氧化物能细化堆焊层胎体金属组织,消除胎体金属的缺陷,细化胎体金属断口韧窝并使撕裂棱数量增加,提高堆焊层冲击韧性和塑性,促使金属基陶瓷与胎体金属界面成多晶过渡区和局部非晶态物相,提高界面的结合强度,稀土氧化物的加入对胎体金属显微硬度的影响不大,但能显著提高堆焊层干摩擦磨损状态下的耐磨性,具有一定的减摩作用。     

Development of a sustained-release matrix tablet formulation of DHEA as ternary complex with α-cyclodextrin and glycine

Sustained-release matrix-tablets of dehydroepiandrosterone (DHEA) as ternary complex with α-cyclodextrin and glycine (c-DHEA) were prepared by direct compression with suitable excipients. The influence of the swelling properties of hydroxypropylmethylcellulose (HPMC) and the disintegrating power of Explotab^® used in combination, as well as the effect of the presence, type and amount of suitable channelling agents (Emcocel^® and spray-dried lactose, alone or in combination) on drug release behaviour from matrix-tablets has been evaluated. The best performances in terms of drug release was obtained from formulations containing a 75:25 w/w spray-dried lactose:Emcocel^® combination in the presence of HPMC as matrix-forming polymer, leading to a more than 65% DHEA released at the end of the test, a value which was, respectively, 1.9 and 2.7 times higher than those achieved with the corresponding formulations containing spray-dried lactose or Emcocel^® alone. The drug release profile from the most effective matrix-tablet formulation of c-DHEA allowed achievement of a more than 6-fold increase in the drug amount released within 24 h in comparison with the same formulation containing the simple physical mixtures of DHEA, α-cyclodextrin and glycine. Therefore the advantage of using DHEA as ternary complex, prepared by mechano-chemical treatment, was clearly demonstrated, thus allowing the development of an effective sustained-release formulation of the drug.     

Microstructure and properties of polyacrylonitrile based carbon fibers

The microstructure of polyacrylonitrile (PAN)-based carbon fibers with different mechanical properties was investigated. It was found that the tensile strength of the PAN-based carbon fibers generally decrease with the increase in the modulus. The properties of PAN-based carbon fiber are mainly controlled by the microstructure and microvoids. The increase in size and orientation of graphite crystallites follows the decrease in interlayer space of graphite sheets, which accompanies the increase in modulus and decrease in tensile strength of the carbon fibers. Simultaneously, the increase in the modulus of the carbon fibers accompanies the merging of the elliptical microvoids along the fiber axis and the turbostratic graphite in the carbon fibers transforms into 3D ordered graphite lamellar structure. This work provides useful information on tailoring the mechanical properties of carbon fibers by adjusting the microstructure.     

Annealing induced microstructure and mechanical property changes of impact resistant polypropylene copolymer

The effects of annealing on microstructure and mechanical properties of an impact resistant polypropylene copolymer(IPC) were investigated. Different annealing temperatures ranging from 80 °C to 160 °C were selected. The phase reorganization of IPC during annealing process was studied through morphological characterization technologies, including scanning electron microscopy(SEM) and transmission electron microscopy(TEM). The crystalline structure changes in the IPC sample, including the i PP matrix and PE component, were investigated using wide angle X-ray diffraction(WAXD) and differential scanning calorimetry(DSC). Dynamic mechanical analysis(DMA) was used to analyze the relaxation extent of IPC before and after annealing. The results showed that annealing induced phase reorganization in IPC and the degree of phase reorganization depended on annealing temperature. The annealed IPC samples exhibited largely increased crystallinity compared with the unannealed one. Intensified damping peak with increased molecular chain mobility was achieved for the annealed IPC samples. At an appropriate annealing temperature(140 °C), largely enhanced impact strength was achieved for the annealed IPC sample. The toughening mechanisms were analyzed based on the phase reorganization and relaxation behavior.     

Structural arrangements of the ternary metal boride carbide compounds MB2C4 (M=Mg, Ca, La and Ce) from first-principles theory

The structural arrangements of the ternary metal borocarbides MB₂C₄ (M=Mg, Ca; La and Ce) are investigated using density-functional theory (DFT) calculations within the generalized gradient approximation (GGA). Results indicate that these compounds adopt a layered structure consisting of graphite-like B₂C₄ layers alternating with metal sheets. Within the hexagonal layers, the coloring with the -C-C-C-B-C-B- sequence is energetically more stable than that with the -C-C-C-C-B-B- one. The electronic structures of these compounds, mainly determined by the B₂C₄ sheets, can be rationalized with the simple valence electron distribution M²⁺[B₂C₄]²⁻xe⁻, with the metals essentially acting as two-electron donors with respect to the boron-carbon network, the other x electrons remaining in the relatively narrow d and/or f bands of the metals. Accordingly, MB₂C₄ are narrow band-gap semiconductors (ΔE≈0.2-0.4 eV) with M=Mg and Ca. On the other hand, with M=La and Ce, the compounds are conducting with a relatively high density of states at the Fermi level predominantly metal in character with substantial B/Cπ* antibonding state admixture.     

New examples of ternary rare-earth metal boride carbides containing finite boron-carbon chains: The crystal and electronic structure of RE15B6C20 (RE=Pr, Nd)

The ternary rare-earth metal boride carbides RE₁₅B₆C₂₀ (RE=Pr, Nd) were synthesized by co-melting the elements. They exist above 1270 K. Their crystal structures were determined from single-crystal X-ray diffraction data. Both crystallize in the space group P1¯, Z=1, a=8.3431(8) Å, b=9.2492(9) Å, c=8.3581(8) Å, α=84.72(1)°, β=89.68(1)°, γ =84.23(1)° (R1=0.041 (wR2=0.10) for 3291 reflections with I_o>2σ(I_o)) for Pr₁₅B₆C₂₀, and a=8.284(1) Å, b=9.228(1) Å, c=8.309(1) Å, α=84.74(1)°, β=89.68(1)°, γ=84.17(2)° (R1=0.033 (wR2=0.049) for 2970 reflections with I_o>2σ(I_o)) for Nd₁₅B₆C₂₀. Their structure consists of a three-dimensional framework of rare-earth metal atoms resulting from the stacking of slightly corrugated and distorted square nets, leading to cavities filled with unprecedented B₂C₄ finite chains, disordered C₃ entities and isolated carbon atoms, respectively. Structural and theoretical analyses suggest the ionic formulation (RE³⁺)₁₅([B₂C₄]⁶⁻)₃([C₃]⁴⁻)₂(C⁴⁻)₂·11ē. Accordingly, density functional theory calculations indicate that the compounds are metallic. Both structural arguments as well as energy calculations on different boron vs. carbon distributions in the B₂C₄ chains support the presence of a CBCCBC unit. Pr₁₅B₆C₁₈ exhibits antiferromagnetic order at T_N=7.9 K, followed by a meta-magnetic transition above a critical external field B>0.03 T. On the other hand, Nd₁₅B₆C₁₈ is a ferromagnet below T_C≈40 K.