厚煤层一次采全高煤壁失稳原因及控制技术

针对成庄煤矿四盘区层一次采全高煤壁失稳问题,对观测统计数据进行分析,发现片帮主要表现形式分五种:顶部、腰部、顶底部、底部以及斜切片帮,据此采用对顶板超前预爆破和煤壁超前预加固技术来控制大采高煤壁稳定性,不仅对煤壁失稳的控制取得了良好的效果,而且经济效益显著。可为相似条件下的厚煤层一次采全高煤壁失稳控制提供借鉴。     

AZ31镁合金薄板经不同累积应变的连续弯曲变形后的显微组织与成形性能

对AZ31镁合金板材进行不同累积应变的连续弯曲变形及退火处理,随后对显微组织与力学性能的变化进行了研究。结果表明:经不同累积应变的连续弯曲变形后,镁合金板材的显微组织中没有发现孪晶,退火后,板材表层的晶粒异常长大,粗晶层的厚度随着累积应变的增加而增加,并且镁合金板材的织构朝RD方向偏转,偏转角度随累积应变的增加而增大;与原始板材相比,连续弯曲变形及退火处理使镁合金板材呈现出较好的室温成形性能(杯突值由2.3 mm提高到4.9 mm,提高了~113%),这主要归因于基面织构的改善使镁合金板材的r值减小与n值增大。     

Preparation of near net size porous alumina-calcium aluminate ceramics by gelcasting-pore-forming agent processs

In the processing of porous ceramics, shrinkage from green body to sintered compact during drying and sintering is one of the key concerns which affect microstructure and properties of porous ceramics. Through releasing gases from the burning of the pore forming agents, and volume expansion from the formation of low density resultants during sintering, the sintering shrinkage can be effectively compensated and near net size preparation can be achieved. Herein, near net size porous alumina-calcium aluminate ceramics with controllable shrinkage have been prepared using a combination of gelcasting and pore-forming agent process by adjusting the amount of CaCO₃ and polymethyl methacrylate (PMMA) microspheres added. Al₂O₃ and CaCO₃ were used as raw materials, PMMA microspheres were used as pore-forming agent, isobutylene/maleic anhydride copolymer (Isobam104) was used as gelling agent and dispersing agent. The effects of the addition amounts of CaCO₃ and PMMA in the slurry on the phase composition, shrinkage, porosity, and strength of porous alumina-calcium aluminate ceramics were investigated. The results show that as the CaCO₃ addition amount increases from 0 to 20 wt%, the shrinkage of the samples gradually decreases from 7.3% to −1.4%, and the consequent porosity increases from 58% to 66%, while the compressive strength increases from 5.9 to 15.5 MPa. When PMMA content increases from 10 to 50 wt%, the shrinkage of the samples decreases first and then increases, the porosity increases from 51% to 74%, and the compressive strength decreases from 12.5 to 5.3 MPa. The mechanisms for controlling shrinkages during preparation of porous alumina-calcium aluminate ceramics can be attributed to the following aspects: on one hand, gas release from burning of PMMA and decomposition of CaCO₃ during sintering; on the other hand, volume expansion due to the formation of lower density calcium aluminates which come from the reactions between CaO and Al₂O₃. The near net size preparation technique is of great significance for the manufacture of porous ceramics since the subsequent machining cost can be effectively reduced.     

近距离煤层煤柱下应力分布和巷道支护技术

针对和尚嘴煤业近距离煤层煤柱下掘进巷道变形大的问题,在介绍地质力学特征的基础上,采用数值模拟分析上部煤层不同方式采动后,采空区和煤柱在下部煤层的应力分布情况。分析煤柱下巷道变形特点和支护要点,结合高预应力强力锚杆支护理论,提出合理的锚网与锚索联合支护设计,现场试验效果明显。     

Calorimetric study of ytterbium orthovanadate YbVO4 polycrystalline ceramics

The heat capacity of ytterbium orthovanadate was first measured by adiabatic calorimetry in the temperature range T?=?12.28–344.06?K. No obvious anomalies were observed on the curve obtained. The values of standard thermodynamic functions in the temperature range T?=?0–400 K were calculated. Based on low-temperature calorimetry data obtained, previously published data on the high-temperature heat capacity of ytterbium orthovanadate were corrected. The anomalous contribution to heat capacity for YbVO₄ was compared with the data known for YbPO₄.     

Synthesis and properties of (Hf1-xTax)C solid solution carbides

Thermodynamically stable (Hf_1–xTa_x)C (x?=?0.1–0.3) compositions were selected by First Principle Calculation and synthesized in nanopowders via high-energy ball milling and carbothermal reduction of commercial oxides at 1450?°C. The formation of a solid solution during powder synthesis was investigated. The solid solution carbide powders were sintered at 1900?°C by spark plasma sintering without a sintering aid. As a result, the (Hf_1–xTa_x)C solid solution carbides exhibited high densities, excellent hardness and fracture toughness (ρ: 98.7–100.0%, HVN: 19.69–19.98?GPa, K_IC: 5.09–5.15?MPa?m^1/2) compared with previously reported HfC and HfC–TaC solid solution carbides.     

Hydrogen production through dry reforming of biogas using a porous electrochemical cell: Effects of a cobalt catalyst in the electrode and mixing of air with biogas

This paper reports the performance of porous Gd-doped ceria (GDC) electrochemical cells with Co metal in both electrodes (cell No. 1) and with Ni metal in the cathode and Co metal in the anode (cell No. 2) for CO₂ decomposition, CH₄ decomposition, and the dry reforming reaction of a biogas with CO₂ gas (CH₄ + CO₂ → 2H₂ + 2CO) or with O₂ gas in air (3CH₄ +?1.875CO₂ +?1.314O₂ → 6H₂ +?4.875CO +?0.7515O₂). GDC cell No. 1 produced H₂ gas at formation rates of 0.055 and 0.33?mL-H₂/(min?m²-electrode) per 1?mL-supplied gas/(min?m²-electrode) at 600?°C and 800?°C, respectively, by the reforming of the biogas with CO₂ gas. Similarly, cell No. 2 produced H₂ gas at formation rates of 0.40?mL-H₂/(min?m²) per 1?mL-supplied gas/(min?m²) at 800?°C from a mixture of biogas and CO₂ gas. The dry reforming of a real biogas with CO₂ or O₂ gas at 800?°C proceeded thermodynamically over the Co or Ni metal catalyst in the cathode of the porous GDC cell. Faraday's law controlled the dry reforming rate of the biogas at 600?°C in cell No. 2. This paper also clarifies the influence of carbon deposition, which originates from CH₄ pyrolysis (CH₄ → C + 2H₂) and disproportionation of CO gas (2CO → C + CO₂), on the cell performance during dry reforming. The dry reforming of a biogas with O₂ molecules from air exhibits high durability because of the oxidation of the deposited carbon by supplied air.     

Preparation of nanocrystalline MoSi2 with enhanced lithium storage by sol–gel and carbonthermal reduction method

Herein nanocrystalline MoSi₂ with enhanced lithium storage was successfully synthesized via a sol-gel and carbonthermal reduction method. Reduction of the gel mixture of Mo precursor and Si precursor by carbon at a desired temperature resulted in the formation of MoSi₂ nanoparticles. The gel mixture was obtained through the hydrolysis of TEOS and ammonium molybdate and the polymerization of hydrolysis products of TEOS. The reducing agent carbon was produced via decarburition of sucrose's hydrolysis products, which have been wrapped in the gel during its formation process. Addition of HCl to the mixed solution controlled the hydrolysis and polymerization rate, and enabled the formation of a gel mixture with homogeneously distributed hydrolysis products of ammonium molybdate, TEOS and sucrose. This achievement likely generates a novel route to synthesize non-oxide compounds such as silicide, carbide through the sol–gel and carbonthermal reduction process. In addition, the as-received MoSi₂ nanoparticles showed considerable activities in the reversible lithiation and delithiation process. When using as an anode for Li-ion batteries, MoSi₂ nanoparticles delivered a specific capacity of 325 mAh g^?1 at C/12 and showed an increasing capacity with cycling.     

CO2 laser-assisted preparation of transparent Eu2Ti2O7 thin films

We present a laser-assisted preparation of transparent europium-titanate Eu₂Ti₂O₇ thin films with tailored structural and optical properties. We have evaluated the effects of the irradiation time on the structural and the optical properties of the films. This approach allows the preparation of nanocrystalline crack-free films and micro patterns. The amorphous thin films were prepared by a sol-gel method. The films were annealed by a CO₂ laser beam for various time intervals. The laser irradiation induced a crystallization process that resulted in the formation of Eu₂Ti₂O₇ nanocrystals. The nanocrystals regularly grew with increasing irradiation time reaching the size from 25?nm to 45?nm. A film of a thickness 480?nm exhibited an optical transmission of 91.9% that is close to the maximal theoretical limit. The film's refractive index at 632?nm was 2.26. A micrometric pattern was prepared by a direct laser writing followed by a wet chemical etching. Feasibility of the demonstrated approach, together with the high film's quality, and europium-titanate chemical resistivity open up many opportunities for advanced applications. The approach can be used for a preparation of protective coatings and integrated photonic devices such as planar optical waveguides and couplers.     

Green preparation of in situ Cr3C2 nano-coatings on graphite surface and their water-wettability and rheological properties

Cr₃C₂ coatings were successfully prepared on the surface of graphite flakes via a molten salt route by mixing Cr powders with natural graphite flakes in a binary LiCl-KCl salt at 450–950?°C for 4–12?h. The phases and microstructures of the coatings were verified by its XRD/XPS spectra and SEM/AFM observations, respectively. Together with the dissolution/dispersion evidence of chromium powders after interaction with the salt, and the slightly increased particle sizes due to the formation of Cr₃C₂ coatings on graphite flakes, a ‘template-growth’ kinetic process was therefore proposed on the formation of such coatings in the molten salt. The resultant coatings decreased the contact angle between water and graphite from 101° to ~ 75° and lowered the apparent viscosities of graphite water slurry by two orders of magnitude accordingly, suggesting that the coatings will afford graphite with good processing abilities for carbon-water based materials.