以资源整合重组助推南山矿下属集体企业转型发展的新探索

为解决南山矿下属集体企业面临的人员老化严重、生产装备落后、职工就业压力大等发展难题，探索了以资产整合、业务整合、人员整合和管理整合四位一体的资源整合重组新模式，扭转了企业经营困局，维护了矿区和谐稳定，促进了企业转型发展，对同类矿山具有良好的借鉴作用。      

Excitonic Properties of Chemically Synthesized 2D Organic–Inorganic Hybrid Perovskite Nanosheets

2D organic–inorganic hybrid perovskites (OIHPs) represent a unique class of materials with a natural quantum‐well structure and quasi‐2D electronic properties. Here, a versatile direct solution‐based synthesis of mono‐ and few‐layer OIHP nanosheets and a systematic study of their electronic structure as a function of the number of monolayers by photoluminescence and absorption spectroscopy are reported. The monolayers of various OIHPs are found to exhibit high electronic quality as evidenced by high quantum yield and negligible Stokes shift. It is shown that the ground exciton peak blueshifts by ≈40 meV when the layer thickness reduces from bulk to monolayer. It is also shown that the exciton binding energy remains effectively unchanged for (C₆H₅(CH₂)₂NH₃)₂PbI₄ with the number of layers. Similar trends are observed for (C₄H₉NH₃)₂PbI₄ in contrast to the previous report. Further, the photoluminescence lifetime is found to decrease with the number of monolayers, indicating the dominant role of surface trap states in nonradiative recombination of the electron–hole pairs.     

Enhanced hydrogen storage performance of three-dimensional hierarchical porous graphene with nickel nanoparticles

Three-dimensional hierarchical porous graphene with nickel nanoparticles (3DHPG-Ni) was synthesized through electrostatic assembly method with the assistance of poly (methyl methacrylate) (PMMA) template and subsequent removal of PMMA template by calcination. The morphology, microstructure and hydrogen adsorption properties of 3DHPG-Ni nanocomposites were examined in detail. The obtained 3DHPG-Ni nanocomposite exhibited hierarchical porous structure composed of macro-, meso- and micropores, high specific surface area (925 m² g^?1), large pore volume (0.58 cm³ g^?1) and excellent hydrogen storage capacity. Under the pressure of 5 bar, 3DHPG-Ni nanocomposite showed a maximum hydrogen capacity of 4.22 wt% and 1.95 wt% at 77 K and 298 K, respectively, demonstrating that the as-prepared 3DHPG-Ni nanocomposite was supposed to be a promising material with outstanding properties for practical applications in the field of hydrogen storage. The three-dimensional hierarchical porous structure, evenly distributed Ni nanoparticles and hydrogen spillover effect were responsible for the enhanced hydrogen storage capacities.     

水电站大型竖井施工安全风险控制措施研究

竖井是大型水电工程中广泛采用的重要建筑物,但竖井的传统施工方法存在施工程序复杂、人工劳动强度大、施工效率不高等特点,同时还存在较大的安全风险。通过对杨房沟水电站大型竖井施工过程的研究,总结出精细化控制爆破、小溜渣井施工方式,同时也设计了一套用于运输的综合提升系统。采用上述创新方法不仅减少了繁琐的施工程序,降低了安全施工风险,而且大量采用机械化手段进一步提高了施工效率,确保了该工程竖井施工的安全风险可控。相关措施可为类似工程的竖井施工提供较好的借鉴作用。     

融合环境因素的有限空间毒气扩散危害程度分析

为探究环境因素对毒气扩散危害程度的影响,通过对比有限空间内外环境差异,了解气体在有限空间内受力情况,并以传统高斯烟羽模型为基础,考虑扩散气体与有限空间边界碰撞产生的反射作用,建立了适用于有限空间气体扩散的改进高斯烟羽模型。深度剖析有限空间气体扩散环境,挖掘气体扩散主要关联因子,构建风速、地表粗糙度对有限空间气体扩散的影响函数;参照有限空间环境特征,分别设置3种不同风速与2种不同地表粗糙度,推求6种不同环境条件下气体扩散面积,阐明风速与地表粗糙度对有限空间气体扩散的影响程度。结果表明:在单一风速条件下,风速越高,地表粗糙度越低,洞室内H2S气体滞留时间越短,洞室内气体的扩散面积越小;风速越低,地表粗糙度越高,洞室内气体的扩散面积越大。     

微裂隙中水泥浆液渗滤效应的可视化试验研究

在微裂隙岩体注浆过程中,水泥浆液的渗滤效应对注浆效果的影响显著。自主研制了一套微裂隙注浆可视化试验系统,该系统由注浆系统、微裂隙模型以及监测系统3个部分组成,监测系统又分为显微监测系统和压力流量监测系统。当水泥浆液进入微裂隙模型后,利用显微监测系统对裂隙入口处的渗滤效应进行实时观测。利用压力流量监测系统对注浆试验过程中的注浆压力以及累计流量进行自动记录。运用自主设计的微裂隙注浆可视化试验系统,对微裂隙中的水泥浆液渗滤过程进行试验研究。采用3种水泥浆材(超细水泥Ⅰ、超细水泥Ⅱ和普通水泥),研究在注浆压力2.0 MPa、水灰比1.0的条件下,不同水泥颗粒粒径大小在不同裂隙开度下的浆液渗滤效应。通过试验发现,当裂隙开度较小时,在裂隙入口处形成了完整的半圆拱形滤饼;随着裂隙开度的增加,在裂隙入口处形成断续分布状滤饼;当裂隙开度增加到无渗滤发生时,裂隙入口处仅残留少量水泥颗粒附着物。通过试验获得了3种水泥的最小可注入裂隙开度大小b min和最小无渗滤裂隙开度大小b crit:超细水泥Ⅰ的b min和b crit分别为80和280μm;超细水泥Ⅱ的b min和b crit分别为100和300μm;普通水泥的b min和b crit分别为140和310μm。研究结果发现水泥粒径的减小对最小可注入裂隙开度大小的影响较大,但对最小无渗滤裂隙开度大小的影响较小。结合渗滤趋势k值,发现随着水泥粒径的减小,相应的k min和k crit值会随之增加,水泥浆液更容易在裂隙入口处发生渗滤,这是因为超细水泥比表面积更大,水泥颗粒间易发生团聚。     

Effect of Mo on corrosion behavior of Ni20Cr–xMo alloys in air with NaCl–KCl–CaCl2 vapor at 570°C

The effect of Mo on the corrosion behavior of Ni20Cr–xMo alloys in an oxidizing chlorine-containing atmosphere using air mixed with the salt-vapor mixture of NaCl–KCl–CaCl₂ at 570°C was investigated. The results revealed that the corrosion performance of the Ni20Cr alloys in the oxidizing chlorine atmosphere was improved by Mo addition of up to 3 wt%. The Mo-free alloy formed a potassium chromate during corrosion as a result of the reaction between the Cr₂O₃ scale and KCl vapor. The chromate formation increased the chlorine potential at the scale surface and induced the breakdown of the protective Cr₂O₃ scale, resulting in internal chromium chloride precipitates and a Cr-depleted zone. In contrast, the presence of Mo resulted in the formation of a NiO scale, which did not react with the salt vapors and, therefore, prevented the formation of chromates. The beneficial effect of Mo on the high-temperature chlorination of Ni–Cr alloys in salt-vapor-containing atmospheres was ascribed to the suppression of chlorine generation due to NiO scale formation.     

Study of the Antioxidative Properties of Several Amino Acid-Type Surfactants and their Synergistic Effect in Mixed Micelle

Cysteine and methionine, two sulfur-containing amino acids (AA), were introduced in their surfactant forms as potential antioxidants. The antioxidative (AOX) properties of lauroyl methionine (C12-Met) and lauroyl cysteine (C12-Cys) was investigated by means of the oxygen radical absorbance capacity assay. Both the surfactants exhibited excellent AOX behavior at the premicellar state and micellar medium. The AOX behavior was found to be comparable for both the surfactants at their premicellar states. However, in micellar medium, C12-Met showed better AOX property than C12-Cys. The AOX power of the surfactants was compared with other previously developed AA-type surfactants. The order of the AOX power was found to be: C12-tryptophan > C12-tyrosine ≈ C12-methionine ≈ C12-cysteine > C12-histidine at the premicellar state and C12-tryptophan > C12-tyrosine > C12-methionine > C12-cysteine > C12-histidine at the micellar state. C12-Cys displayed lower AOX property in micellar medium due to its dimer formation tendency. Based on the HPLC and UPLC-Q-TOF-MS analysis, the dimer formation of C12-Cys was found to be accelerated due to the micellar environment and results into negative synergistic effect on other aromatic AA-type surfactants. However, the presence of C12-His in the micellar solution of C12-Cys resulted no synergistic effect due to stronger H-bonding between the surfactants and resulting less dimer formation.     

Phase-transition induced optimization of electrostrain,electrocaloric refrigeration and energy storage of LiNbO3 doped BNT-BT ceramics

((Bi_0.5Na_0.5TiO₃)_0.88-(BaTiO₃)_0.12)_(1-x)-(LiNbO₃)_x (x = 0.0, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, and 0.07; abbreviated as LiNbO₃-doped BNT-BT) ceramics possessing many excellent performances (large electrostrain, negative electrocaloric effect and energy storage density with high efficiency) was fabricated by the conventional solid-state reaction method. A large electrostrain (maximum ~ 0.34% at 100 kV/cm and room temperature) with high thermal stability over a broad temperature range (~80 K) is obtained at x = 0.03. A large energy storage density (maximum W_energy ~ 0.665 J/cm³ at 100 kV/cm and room temperature) with a high efficiency (η ~ 49.3%) is achieved at x = 0.06. Moreover, a large negative electrocaloric (EC) effect (maximum ΔT ~ 1.71 K with ΔS ~ - 0.22 J/(K kg) at 70 kV/cm)) is also obtained at x = 0.04. Phase transition (from ferroelectric to antiferroelectric and then to relaxor) induced by increasing the doping amount of LiNbO₃ plays a very key role on the optimization of these performances. These findings and breakthroughs make the LiNbO₃-doped BNT-BT ceramics very promising candidates as multifunctional materials.