高落差粉尘扩散规律和分布特征

高溜井放矿过程中会形成强大的冲击气流引起粉尘扩散，造成严重的井下环境污染，对其进行有效治理一直是井下通风除尘的工作重心，本工作利用相似实验和数值模拟相结合的方式探究溜井放矿过程中粉尘的扩散规律和分布特征。通过改变放矿质量、矿石粒径、溜井密闭程度、含水率等因素测试不同条件下气流大小和粉尘浓度分布，并利用CFD-DPM耦合方法模拟卸矿过程中的气?固两相流，研究气流和粉尘浓度时空分布特征。结果表明，最大粉尘浓度和风速随放矿质量增加而上升，随颗粒粒径和溜井密闭程度增大而降低，且含水率越大，粉尘浓度越小，风速无明显变化，在放矿过程中矿石颗粒之间碰撞占主导作用，颗粒流呈横向分布。     

整体壁板离散填料滚弯成形有限元模拟

具有一定曲率外形的铝合金整体壁板属于典型的多筋零部件,传统弯曲成形工艺成形困难,容易产生多种缺陷。提出了离散填料辅助滚弯成形整体2A12T4铝合金壁板滚弯工艺,并通过实验与整体填料滚变成形进行了对比,同时采用有限元模拟技术,探究了离散填料辅助整体壁板滚弯成形中的影响因素。研究结果表明:填料数量、上下垫板厚度等因素对成形性能影响较大,填料在3~6块时成形稳定,可以有效地避免筋条屈曲与失稳;随垫板厚度增加,壁板表面圆弧更加光滑、连续,但是回弹性增强;上下垫板分别在10~20 mm厚度时,综合性能较好。通过离散填料辅助滚弯技术可以成形出质量较高的整体壁板。     

截点法测量金属平均晶粒度的不确定度评定及分析

分别利用金相显微镜目镜和金相分析软件手动计数测量的方式，采用截点法对均匀等轴晶粒的平均晶粒度结果测量不确定度进行评定研究，分析影响其测量不确定度的主要来源。结果表明:目镜测量平均晶粒度的平均截距值为35.7 μm，U=2.1 μm，k=2；金相分析软件测量平均晶粒度的平均截距值为35.5 μm，U=0.4 μm，k=2。金相显微镜放大倍率偏差致使试验线长度引入的不确定度分量是应用目镜测量平均晶粒度结果不确定度的主要来源；而使用金相分析软件手动测量平均晶粒度结果测量不确定度主要来源，却是由测量的晶界与试验线的交点数的不确定度分量引入的。在其他条件均相同的情况下，使用金相分析软件手动测量平均晶粒度比应用目镜直接测量平均晶粒度，更能缩小结果在相同包含概率下不确定性的范围，提高准确度。而对于均匀等轴晶粒的平均晶粒度测量，直线截点法和圆截点法对最终的不确定度的评定结果影响不大。     

山东栖霞—大柳行地区金矿找矿靶区地质评价及优选

栖霞—大柳行地区位于胶东中部栖霞—蓬莱金矿成矿带内，是胶东重要的金成矿区，成矿条件优越。为了对圈定靶区进行优选分类，通过对该区地质背景、找矿靶区评价、找矿靶区优选方面展开综合研究，并结合勘查工作程度和矿业权设置情况，划分出3类预测区，选定了5个靶区为今后优先部署勘查工作的方向。     

基于目标级联技术的含风电互联电网机组组合策略

针对含风电互联电网日前安全约束机组组合的规模大、约束复杂、求解困难等问题,提出基于目标级联分析技术的分散协调优化策略。将问题分解为负责区域间边界节点电压相角协调的上层优化问题和以并行方式独立优化各区域发电计划的下层优化问题。下层优化以弃风电量期望和电量不足期望,量化各区域内风电、负荷预测误差,以及常规机组强迫停运等系统运行不确定性所带来的风险,并以罚函数的形式引入目标函数,以综合优化系统可靠性与经济性。2区域12节点系统和IEEE RTS96三区域互联系统算例仿真验证所建模型和算法的有效性。     

Effects of stray AC on corrosion of 3-layer polyethylene coated X70 pipeline steel and cathodic delamination of coating with defects in 3.5 wt-% NaCl solution

In this work, the effects of stray alternating current (AC) on the corrosion of coated X70 pipeline steel and the delamination of 3-layer polyethylene (3PE) coatings with defects were investigated using COMSOL Multiphysics simulation, electrochemical impedance spectroscopy and three-dimensional (3D) digital microscope techniques. The results showed that under the same level of AC interference, pits with deeper maximum pit depth were observed at the smaller defect areas than those at larger defect areas. It was consistent with the simulation results that a greater corrosion current density was accompanied on samples with smaller defects. According to 3D digital images, the larger delamination of 3PE coatings was found on samples with smaller defects. With the increase of current density, the impedance of samples with small defects decreased, while that of samples with large defects increased. Additionally, with the same defect size, the maximum pit depth became deeper and the corrosion was more severe.     

Microstructure and mechanical properties of TiC0.7N0.3-HfC cermet tool materials

TiC_0.7N_0.3-HfC cermet tool materials were fabricated by hot-press sintering. Effects of different metal additives (Ni, Co, Ni-Co and Ni-Mo), sintering temperature and holding time on the microstructures and mechanical properties of TiC_0.7N_0.3-HfC cermets were investigated. Results showed that Ni-Mo or Ni-Co as metal additives was better for the mechanical properties of TiC_0.7N_0.3-HfC cermets than only Ni or only Co as the metal additives and Ni-Mo better than Ni-Co. HfC particle dispersion existed in these four cermets and only in the TiC_0.7N_0.3-HfC-Ni-Mo cermet the core-rim structure obviously existed. TiC_0.7N_0.3-HfC-Ni-Mo cermet had significantly smaller grains than the other three cermets because Ni-Mo can significantly refine the grain. With the sintering temperature increasing from 1450?°C to 1650?°C, grains grew gradually; Vickers hardness and flexural strength decreased gradually and the fracture toughness increased firstly and then decreased. With the holding time increasing from 15?min to 60?min, grains grew gradually; Vickers hardness, flexural strength and the fracture toughness increased firstly and then decreased. TiC_0.7N_0.3-HfC-Ni-Mo cermets sintered at 1450?°C with 30?min holding time had the better comprehensive mechanical properties with flexural strength of 1346.41?±?31?MPa, fracture toughness of 8.46?±?0.23?MPa?m^1/2 and Vickers hardness of 22.91?±?0.22?GPa.     

Embedding Ag or Au nanoparticles within the nano-sized wall of YbPO4:Er3+ inverse opals and resulting enhanced upconversion luminescence

Metal nanoparticles preparation in the interior of nanoscale skeleton of inverse opals made up of crystallized matrix is more difficult than the preparation of pure inverse opals. In the present work, the Ag or Au nanoparticles embedded YbPO₄:Er³⁺ inverse opals were prepared by a simple approach, which involved the infiltration of opal template by using the transparent YbPO₄:Er³⁺ sol including silver nitrate or chloroauric acid and the sintering at high temperature. The 20–30?nm Au or 5–10?nm Ag nanoparticles were formed in the interior of nanoscale skeleton in the YbPO₄:Er³⁺ inverse opals, and the Ag or Au nanoparticles embedded YbPO₄:Er³⁺ inverse opals were prepared. The influence of Ag or Au nanoparticles on the upconversion photoluminescence of YbPO₄:Er³⁺ inverse opal was studied, and the upconversion luminescence enhancement induced by the Ag or Au nanoparticles was observed. The mechanisms of upconversion luminescence enhancement of YbPO₄:Er³⁺ inverse opals induced by Ag or Au nanoparticles were discussed. The enhancement of upconversion luminescence induced by Ag nanoparticles was attributed to the enhancement of the excitation field, and the enhancement of upconversion emission induced by Au nanoparticles was related to the increasing of the radiation decay rate of Er³⁺.     

Control of aluminum phosphate coating on mullite fibers by surface modification with polyethylenimine

Aluminum phosphate (AlPO₄) is a promising oxidation-resistant and weak interface for ceramic-matrix composites. In this research, AlPO₄ coating was deposited on mullite fibers by an improved liquid-phase method based on electrostatic attraction. A cationic polyelectrolyte, polyethylenimine (PEI), was used for surface modification of mullite fibers. The formation process, phase evolution and microstructure of the coating were studied. The zeta potential of AlPO₄ particles, PEI-adsorbed AlPO₄ particles, and PEI-adsorbed mullite particles was characterized to find the proper pH value for improving electrostatic attraction. The obtained AlPO₄ coating was porous and continuous, whose thickness could be controlled by multiple coating cycles. The relatively low calcination temperature (600 or 1000 °C) was a useful heat treatment method to develop bonding between coating and fiber as well as reduce the fiber strength degradation. The phase transformations of AlPO₄ have little volume change, and cristobalite AlPO₄ is thermal compatible with mullite. Therefore, the coating structure was preserved after calcining at 1200 °C. The technique is also applicable for other fibers contained mullite phase to fabricate high-performance AlPO₄ coated mullite/mullite composites.     

In-situ preparation of cross-linked hybrid anion exchange membrane of quaternized poly (styrene-b-isobutylene-b-styrene) covalently bonded with graphene

Introducing graphene into polymer matrix is an effective way to enhance performances of anion exchange membrane (AEM). However, utilizing the advantages of graphene by physical approach is limited due to the weak interface interaction between graphene and polymer matrix. Herein, we report an effective strategy to covalently bond graphene with polymer matrix to improve the interface interaction and further to improve the properties of AEM. A series of cross-linked quaternized graphene-based hybrid AEM were fabricated by covalently bonding poly (vinylbenzyl chloride) grafted graphene (GN-g-PVBC) copolymer with chloromethyl functionalized poly (styrene-b-isobutylene-b-styrene) (SIBS) through the cross-linker (N,N,N′,N′-tetramethyl-1,6-hexanediamine) by in-situ synthetic approach. The interface interaction between graphene and QSIBS is greatly enhanced according to micromorphology characterization of the hybrid membrane. The cross-linked quaternized hybrid AEM containing 0.55 wt% of GN-g-PVBC exhibits obviously improved dynamical mechanical properties (storage modulus: 418 MPa), ion conductivity (1.81 × 10² S cm^?1), methanol barrier property (5.19 × 10^?7 cm² s^?1), selectivity (3.49 × 10⁴ S s cm^?3) at 60 °C and especially a comparably excellent chemical stability to that of Nafion 115 due to the enhanced interface interaction between graphene and the polymer matrix.