城市埋地管线的安全风险评估研究

在城市建设过程中,建筑物与构筑物的安全问题始终占据首位,城市埋地管线的安全问题日益严峻.重点探讨城市埋地管线第三方破坏因素对埋地管线的影响,利用模糊层次分析法,确定因素集,建立判断矩阵并进行各因素的权重求解,通过可拓学原理建立节域物元、关联度和等级评价体系,对计算结果进行等级评价,得出在第三方破坏因素影响下城市埋地管线的安全风险等级,所得到的结论对埋地管线施工的安全问题有一定的指导意义.     

A simple design approach to analyse the piled embankment including tensile reinforcement and subsoil contributions

There is not one generally accepted approach for the design of geogrid-reinforced pile-supported (GRPS) embankments. Relevant mechanisms include arching of the embankment material, but also the effect of geogrid reinforcement and potentially a contribution from the underlying subsoil. This paper presents a simple design approach to identify the contribution of all three mechanisms, in which the contribution of multi-layered geogrid reinforcement is also presented. To validate the theoretical predictions for the effect of geogrid reinforcement and the potential contribution of underlying subsoil, a series of three-dimensional finite element analyses are conducted. It is found that a point of ‘maximum arching’ is increased with the height of embankment. This study also presents that the reinforcement could reduce the ultimate stress on the subsoil. However, this requires significant sag of the reinforcement. It is found that the sag of reinforcement is very sensitive to the span of the reinforcement between piles, but relatively insensitive to the stiffness of the reinforcement. For a case with three layers of geogrid, the upper two grids carry relatively little tension compared to the bottom layer. This in turn leads to an approximate but simple equation of vertical equilibrium which may be of use in design.     

BIM技术在大型项目上的应用——以连云港民用机场迁建工程旅客过夜用房酒店为例

在国家政策和市场需求的双重推动下,BIM技术在国内建筑领域迎来快速发展阶段,从最初的概念普及,到能够局部应用,再到现在能够全过程应用,其趋势是十分明确的,但是在其发展的过程中仍然存在着不少问题,如传统技术与BIM技术深入融合问题,BIM技术如何解决工程施工现场实际问题等.本文主要研究BIM技术在连云港民用机场迁建工程旅客过夜用房酒店项目中的综合应用,从协同建模、碰撞检查、管线综合、施工图深化出图及漫游展示等方面着手,着重解决BIM技术在施工过程中应用的落地问题,从而达到提高效率,缩短工期,降低成本,提升质量的目标.     

High chemical stability anion exchange membrane based on poly(aryl piperidinium): Effect of monomer configuration on membrane properties

In recent years, ether-free polyaryl polymers prepared by superacid-catalyzed Friedel-Crafts polymerization have attracted great research interest in the development of anion exchange membranes(AEMs) due to their high alkali resistance and simple synthesis methods. However, the selection of monomers for high-performance polymer backbone and the relationship between polymer structure construction and properties need further investigated. Herein, a series of free-ether poly(aryl piperidinium) (PAP) with different polymer backbone steric construction were synthesized as stable anion exchange membranes. Meta-terphenyl, p-terphenyl and diphenyl-terphenyl copolymer were chosen as monomers to regulate the spatial arrangement of the polymer backbone, which tethered with stable piperidinium cation to improve the chemical stability. In addition, a multi-cation crosslinking strategy has been applied to improve ion conductivity and mechanical stability of AEMs, and further compared with the performance of uncrosslinked AEMs. The properties of the resulting AEMs were investigated and correlated with their polymer structure. In particular, m-terphenyl based AEMs exhibited better dimensional stability and the highest hydroxide conductivity of 144.2 mS/cm at 80 °C than other membranes, which can be attributed to their advantages of polymer backbone arrangement. Furthermore, the hydroxide conductivity of the prepared AEMs remains 80%–90% after treated by 2 M NaOH for 1600 h, exhibiting excellent alkaline stability. The single cell test of m-PTP-20Q4 exhibits a maximum power density of 239 mW/cm² at 80 °C. Hence, the results may guide the selection of polymer monomers to improve performance and alkaline durability for anion exchange membranes.     

Droplet dynamics in a proton exchange membrane fuel cell flow field design with 3D geometry

Water management is crucial to achieve both high-performance and durability of proton exchange membrane fuel cell (PEMFC). Therefore, it is necessary to investigate the dynamic behavior of droplets in PEMFC channel for water management. In this paper, we explore the kinetics of droplets in a 3D flow field by experimental and theoretical analysis. More specifically, we examine the following four perspectives: 1) the movement and falling of droplets, and their force and deformation, 2) the superiority of 3D flow field drainage, 3) the pressure and viscous force under different scenarios including varying droplet sizes and velocities, and 4) the expression describing the shape change of droplets. The results show that the 3D flow field has a greater driving force on droplets and that their deformation affects the discharge of liquid water. Throughout the study, we provide better understanding of droplet dynamic in PEMFC gas channels. It enables to optimize the design and working conditions of these channels.     

Mesoporous g-C3N4 decorated by Ni2P nanoparticles and CdS nanorods together for enhancing photocatalytic hydrogen evolution

Ni₂P nanoparticles and CdS nanorods were grew together on a mesoporous g-C₃N₄ through a facile in-situ solvothermal approach. Under visible light (λ > 400 nm), the as-prepared ternary PCN–CdS-5% Ni₂P composite displays a high H₂ evolution rate with 2905.86 μmol g^?1 h^?1, which is about 14, 18 and 279 times that of PCN–CdS, PCN–Ni₂P and PCN, respectively. The enhanced photocatalytic activity is mainly attributed to the improved separation efficiency of the photocarriers by the type II PCN–CdS heterojunction and the effective extraction of photogenerated electrons by Ni₂P. Meanwhile, Ni₂P acts as co-catalyst to provide the photocatalytic active site for hydrogen reduction. In addition, PCN–CdS-5% Ni₂P composite exerts good stability in 12-h cycles.     

Computational exploration of magnesium-decorated carbon nitride (g-C3N4) monolayer as advanced energy storage materials

Density functional theory (DFT) computational studies were conducted to explore the hydrogen storage performance of a monolayer material that is built on the base of carbon nitride (g-C₃N₄, heptazine structure) with decoration by magnesium (Mg). We found that a 2 × 2 supercell can bind with four Mg atoms. The electronic charges of Mg atoms were transferred to the g-C₃N₄ monolayer, and thus a partial electropositivity on each adsorbed Mg atom was formed, indicating a potential improvement in conductivity. This subsequently causes the hydrogen molecules’ polarization, so that these hydrogen molecules can be efficiently adsorbed via both van der Waals and electrostatic interactions. To note, the configurations of the adsorbed hydrogen molecules were also elucidated, and we found that most adsorbed hydrogen molecules tend to be vertical to the sheet plane. Such a phenomenon is due to the electronic potential distribution. In average, each adsorbed Mg atom can adsorb 1–9 hydrogen molecules with adsorption energies that are ranged from ?0.25 eV to ?0.1 eV. Moreover, we realised that the nitrogen atom can also serve as an active site for hydrogen adsorption. The hydrogen storage capacity of this Mg-decorated g-C₃N₄ is close to 7.96 wt %, which is much higher than the target value of 5.5 wt % proposed by the U.S. department of energy (DOE) in 2020 [1]. The finding in this study indicates a promising carbon-based material for energy storage, and in the future, we hope to develop more advanced materials along this direction.     

A triple (e−/O2−/H+) conducting perovskite BaCo0.4Fe0.4Zr0.1Y0.1O3-δ for low temperature solid oxide fuel cell

Low-temperature solid oxide fuel cells (LT-SOFCs) have recently gained enormous attention worldwide with a new research trend focusing on single layer fuel cells (SLFC), which have better cell performance than traditional SOFCs at low operating temperatures. In this study, a triple (e^?/O^2?/H⁺) conducting perovskite BaCo_0.4Fe_0.4Zr_0.1Y_0.1O_3-δ (BCFZY) is used as the intermediate layer material for SLFC. A high current density of 994 mA/cm² at 0.6 V and a peak power density of 610 mW/cm² with an OCV of 1.01 V has been achieved with a cell operating temperature of 550 °C, confirming the application feasibility of BCFZY in SLFCs. Furthermore, a typical proton conductor BaZr_0.8Y_0.2O_3-δ (BZY) is introduced into BCFZY to enhance the cell performance. By adjusting the mass ratio of the BCFZY-BZY layer, an optimal power density is obtained, achieving 703 mW/cm² with an OCV of 1.03 V at 550 °C with an 8BCFZY:2BZY (wt%) ratio. These findings prove that the proposed BCFZY-BZY holds great promise for developing SLFCs to realize low-temperature operation.     

Hydrogen storage properties of Zr2Co crystalline and amorphous alloys

To further explore the application feasibility of Zr₂Co alloy in tritium-related fields, hydrogenation/dehydrogenation properties of this material of crystalline or amorphous structure, prepared by arc melting or melt spinning, were studied by pressure-composition temperature measurement, X-ray diffraction, differential scanning calorimeter, thermal desorption spectroscopy. It was found that the two kinds of Zr₂Co alloys can absorb hydrogen in a close full concentration of ~9 mmol/g, and may have similar equilibrium hydrogen pressure in the order of 10^?6 Pa at room temperature. In their hydrogenated samples various hydrides were observed to form, including ZrH₂, Zr₂CoH₅, ZrCoH₃ and an amorphous one with gradually decreasing general thermostability. The amorphous alloy exhibited easier hydrogen induced disproportionation caused by highly stable ZrH₂ and much slower hydrogen absorption kinetics. This disproportionation behavior of the crystalline alloy was found to be entirely suppressed by changing heating process. The results firmly indicate that crystalline Zr₂Co alloy could be more favorable for tritium treatment due to very low equilibrium pressure and the feasibility of eliminating the disproportionation.     

Synergistic enhancement of π-electron density in graphitic carbon nitride for significantly improved photocatalytic hydrogen evolution under visible-light irradiation

In this work, a synergistic strategy integrated elemental doping and defect engineering has been developed to modulate the electronic and bandgap structure of g-C₃N₄ by controlling its conjugated aromatic system. Experimental analysis and theoretical calculations con?rm that the generation of imbalanced spatial distributions of charge carriers not only greatly increases the π-electron availability, but also decreases the energy barrier for hydrogen adsorption due to the synergistic effect of the high valence electron of the W dopant and the decreased electronegativity by two-coordinated nitrogen defects, which strengthens the charge transfer efficiency and favors the light capturing capability. The combined bene?ts of the electronic, optical and textural modification lead to a signi?cant improvement of photocatalytic activity of 3.3 mmol h^?1 g^?1 for hydrogen evolution under λ ≥ 400 nm light irradiation, about twentyfold enhancement than that of pristine g-C₃N₄. Such proposed synergistic strategy provides a promising route to promote the performance of g-C₃N₄ for potential applications in solar energy conversion.