Coupling effects of tungsten and molybdenum on microstructure and stressrupture properties of a nickel-base cast superalloy

In order to comprehensively understand the forming mechanism of abnormal phases solidified in a nickel-base cast superalloy with additives of tungsten and molybdenum, the coupling effects of W and Mo on the microstructure and stress-rupture properties were investigated in this paper. The results indicated that the precipitation of primary α-(W, Mo) phase depended tremendously on the amount of W and Mo addition. When the total amount of W and Mo was greater than 5.79 at%, α-(W, Mo) phase became easily precipitated in the alloy.With increasing of Mo/W ratio, the dendrite-like α-(W, Mo) phases were apt to convert into small bars or blockylike phases at the vicinities of γ′/γ eutectic. The morphological changes of α-(W, Mo) phase can be interpreted as the non-equilibrium solidification of W and Mo in the alloy. Since the large sized α-(W, Mo) phase has detrimental effects on stress-rupture properties in as-cast conditions, secondary cracks may mainly initiate at and then propagate along the interfaces of brittle phases and soft matrix. During exposing at 1100 ℃ for 1000 h, the α-(W, Mo) phases transformed gradually into bigger and harder M_6C carbide, which results in decreasing of stress-rupture properties of the alloy. Finally, the alloy with an addition of 14W-1Mo(wt%) maintained the longest stress lives at high temperatures and therefore it revealed the best microstructure stability after 1100 ℃/1000 h thermal exposure.     

Synthesis of polyethylene glycol (PEG) assisted tungsten oxide (WO3) nanoparticles for L-dopa bio-sensing applications

Nanocrystalline tungsten oxides (WO_3−δ) are currently receiving a lot of attention because of their interesting electrical, magnetic, optical and mechanical properties. In this report, we present the synthesis of PEG assisted tungsten oxide (WO₃) nanoparticles by simple household microwave irradiation (2.45 GHz) method. The samples were characterized using powder X-ray diffraction (XRD), thermal analysis (TG/DTA), transmission electron microscopy (TEM), UV-visible diffusion reflectance spectroscopy (UV-VIS-DRS), cyclic voltammetry and electrochemical impedance spectroscopy. Powder XRD results revealed that both the samples prepared with and without surfactant crystallize in the orthorhombic structure corresponding to WO₃·H₂O phase. Subsequent annealing under identical conditions (600 °C/air/6 h) led to significantly different products i.e. monoclinic W₁₇O₄₇ from surfactant free sample and orthorhombic WO₃ from PEG assisted sample. Blue emission was observed through UV-VIS-DRS with blue shift and the band gap energy was estimated as 2.7 and 3.28 eV for PEG assisted as prepared (WO₃·H₂O) and annealed samples (WO₃) respectively. Electrochemical measurements have been performed on all the samples deposited on the surface of glassy carbon (GC) electrode which showed high sensitivity and good selectivity for PEG assisted sample (WO₃·H₂O) for the direct detection of l-dopa.     

Synthesis and structures of silicon-, germanium- and tin-containing tungsten imido alkyl complexes (ArN)2W(CH2EMe3)2 (E = Si, Ge, Sn)

The novel silicon-, germanium- and tin-containing imido alkyl complexes of tungsten of the type (ArN)₂W(CH₂EMe₃)₂ (; E = Si (1), Ge (2), Sn (3)) have been prepared by the reactions of (ArN)₂WCl₂(dme) (dme = 1,2-dimethoxyethane) with heteroelement-containing alkyllithium or Grignard reagents Me₃ECH₂Li (E = Si, Ge), Me₃ECH₂MgCl (E = Ge, Sn). The title compounds were isolated in high yields as crystalline solids and characterized by elemental analysis, IR, ¹H, ¹³C, ²⁹Si and ¹¹⁹Sn NMR spectroscopy and X-ray diffraction studies. The geometry of the W atoms in the compounds can be described as a distorted tetrahedron.     

三山岛金矿采空区地应力测量及其结果分析

采空区上部预留矿柱的回采工作影响到整个矿山的安全生产、采矿方法及其实施.为正确评价上覆岩层和围岩的稳定性情况,采用实现完全温度补偿的空心包体应变技术的套孔应力解除法对三山岛金矿进行地应力测量.建立了矿区地应力场分布模型,获得了三山岛金矿地应力状态和矿区的地应力分布规律.结果表明,三山岛地区地应力场以水平应力为主,符合我国地壳运动的规律.     

N-heterocyclic carbenes as ligands in high-valent molybdenum and tungsten complexes

Oxometal complexes of molybdenum and tungsten in high oxidation states from stable adducts with 1,3-dimethylimidazoline-2-ylidene (L) 1. The first ‘carbene’ complexes of molybdenum(VI) [MoO₂Cl(L)₃]Cl (3a) and tungsten(VI) WO₂Cl₂(L)₂ (4b) are reported.     

Mixed-metal cluster chemistry. 26 . Proclivity for “all-terminal” or “plane-of-bridging-carbonyls” ligand disposition in tungsten-triiridium clusters

Reaction of WH(CO)₃(η-C₅Me₅) with IrCl(CO)₂(4-H₂NC₆H₄Me) affords WIr₃(μ-CO)₃(CO)₈(η-C₅Me₅) in low yield. A structural study reveals a WIr₂-centred plane of bridging carbonyls, in contrast to the crystal structure of WIr₃(CO)₁₁(η-C₅H₅) (all-terminal carbonyl distribution). DFT calculations reveal an increasing proclivity to adopt an all-terminal CO disposition for clusters MIr₃(CO)₁₁(η-C₅H₅) in the gas phase on proceeding from M=Cr to Mo and then W, consistent with structural studies in the solid state for which the tungsten-containing cluster is the only all-terminal example. Increasing electron donation from the ligands in the tungsten system (either from phosphine substitution or cyclopentadienyl permethylation) suffices to impose a plane of bridging carbonyls in the ground state structure. ¹³C NMR fluxionality studies reveal that CO exchange mechanism(s) for WIr₃(CO)₁₁(η-C₅H₅) and the related tetrahedral cluster W₂Ir₂(CO)₁₀(η-C₅H₅)₂ are very fast and involve all carbonyls on the clusters. DFT calculations on MIr₃(CO)₁₁(η-C₅H₅) (M=Cr, Mo) substantiate a ‘merry-go-round’ mechanism for carbonyl scrambling in these systems, a result which is consistent with the scrambling behaviour seen in the NMR fluxionality studies on the W-containing congener.     

New heterodimetallic cyclopentadienyl carbonyl complexes: crystal structure of (C5Me4Et)(μ-CO)3Ru(C5Me5)

A series of heterodimetallic complexes of general formula (C₅R₅)M(μ-CO)₃RuC₅Me₅ (M = Cr, Mo, W; R = Me, Et) has been prepared in good yields by the reaction of [C₅R₅M(CO)₃]⁻ with [C₅Me₅Ru(CH₃CN)₃]⁺. (C₅Me₄Et)W(μ-CO)₃Ru(C₅Me₅) was characterized by a crystal structure determination. The W---Ru bond length of 2.41 Å is consistent with the formulation of a metal-metal triple bond, while the unsymmetrical bonding mode of the three bridging carbonyl groups reflects the inherent non-equivalence of the two different C₅R₅M-units. Using [CpRu(CH₃CN)₃]⁺ or [CpRu(CO)₂(CH₃CN)]⁺ as the cationic precursor leads to the formation of dimetallic species (C₅R₅)M(CO)₅RuC₅H₅ with both bridging and terminal carbonyl groups.     

Organotransition-Metal-Mediated Borane-Cage Expansion

Attempts were made to synthesize dinuclear Group 6 metal complexes of the arachno -octahydrotriborate anion. Specifically, the dimer [CpW(CO) 3 ] 2 (Cp = m 5 -C 5 H 5 ) was employed as the metal reagent. However, the formation of dinuclear metallaborane complexes did not ensue. Rather, clean, rapid, systematic borane-cage expansion was observed. The [B 3 H 8 ] m cluster was quantitatively converted to B 5 H 9 ,[B 9 H 14 ] m , or [B 11 H 14 ] m , or both, depending on reaction conditions. Refluxing a 1:1 mixture of [B 3 H 8 ] m and [CpW(CO) 3 ] 2 in toluene or dioxane lead to the rapid, quantitative conversion of [B 3 H 8 ] m to B 5 H 9 . However, refluxing a 2:1 mixture of [B 3 H 8 ] m and [CpW(CO) 3 ] 2 in the same solvents yielded [B 9 H 14 ] m and [B 11 H 14 ] m as the primary products; when glyme was the solvent, only [B 9 H 14 ] m was observed, even after prolonged heating.     

Analysis of powdered tungsten carbide hard-metal precursors and cemented compact tungsten carbides using laser-induced breakdown spectroscopy

Laser-induced breakdown spectroscopy (LIBS) has been applied to the direct analysis of powdered tungsten carbide hard-metal precursors and cemented tungsten carbides. The aim of this work was to examine the possibility of quantitative determination of the niobium, titanium, tantalum and cobalt. The investigated samples were in the form of pellets, pressed with and without binder (powdered silver) and in the form of cemented tungsten carbides. The pellets were prepared by pressing the powdered material in a hydraulic press. Cemented tungsten carbides were embedded in resin for easier manipulation.

Several lasers and detection systems were utilized. The Nd:YAG laser working at a basic wavelength of 1064 nm and fourth-harmonic frequency of 266 nm with a gated photomultiplier or ICCD detector HORIBA JY was used for the determination of niobium which was chosen as a model element. Different types of surrounding gases (air, He, Ar) were investigated for analysis. The ICCD detector DICAM PRO with Mechelle 7500 spectrometer with ArF laser (193 nm) and KrF laser (248 nm) were employed for the determination of niobium, titanium, tantalum and cobalt in samples under air atmosphere. Good calibration curves were obtained for Nb, Ti, and Ta (coefficients of determination r² > 0.96). Acceptable calibration curves were acquired for the determination of cobalt (coefficient of determination r² = 0.7994) but only for the cemented samples. In the case of powdered carbide precursors, the calibration for cobalt was found to be problematic.     

矿井提升机驱动系统双PWM变频器的应用研究

通过分析传统矿井提升机驱动系统性能上的不足,结合煤矿生产实际,介绍了双PWM变频器在矿井提升机变频驱动系统升级改造中的应用。着重分析了其中PWM整流器在功率因数控制,电能回馈,谐波抑制等方面的优良性能,提出了双PWM变频器在矿井提升机驱动系统上应用的优越性,在样机的基础上进行了实验分析,并创新性地提出了超级电容在PWM整流器直流侧母线的储能滤波应用。