Dynamic Response Solution of Multi-Layered Pavement Structure Under FWD Load Appling the Precise Integration Algorithm

The pavement layered structures are composed of surface layer, road base and multi-layered soil foundation. They can be undermined over time by repeated vehicle loads. In this study, a hybrid numerical method which can evaluate the displacement responses of pavement structures under dynamic falling weight deflectometer (FWD) loads. The proposed method consists of two parts: (a) the dynamic stiffness matrices of the points at the surface in the frequency domain which is based on the domain-transformation and dual vector form equation, and (b) interpolates the dynamic stiffness matrices by a continues rational function of frequency. The mixed variables formulation (MVF) can treat multiple degree of freedom systems with considering the coupling term between degree of freedoms. The accuracy of the developed method has been demonstrated by comparison between the proposed method and published results from the other method. Then the proposed method can be applied as a forward calculation technique to emulate the falling weight deflectometer test for multi-layered pavement structures.     

A study of microstructure and performance of cast Fe–8Cr–2B alloy

The effects of quenching temperature on microstructure and hardness of cast Fe–8Cr–2B alloy containing 0.3 wt% C, 2.0 wt% B, 8.0 wt% Cr, 0.6 wt% Si, and 0.8 wt% Mn were investigated by optical microscopy (OM), scanning electron microscopy (SEM), X‐ray diffraction (XRD), Rockwell hardness and Vickers microhardness testers. The experimental results indicate that the as‐cast microstructure of cast Fe–8Cr–2B alloy consists of M₂B (M = Fe, Cr), M₇(C, B)₃, α‐Fe, and γ‐Fe. The dendritic matrix composed of lath martensite mixed with a small amount of retained austenite, and the netlike boride M₂B distribute in the grain boundary. After quenching between 950 °C and 1100 °C, the netlike eutectic boride are broken up and a new phase‐M₂₃(C, B)₆ which is distributed in the shape of sphere or short rod‐like are precipitated from the matrix. Both the macrohardness and microhardness of specimens increase with the increasing quenching temperature. At about 1050 °C, the hardness reaches the maximum value. However, when the temperature exceeds 1050 °C, the hardness will decrease slightly. With the increase of tempering temperature, the hardness of cast Fe–8Cr–2B alloy quenching from 1050 °C decreases gradually and its impact toughness increases slightly. Crusher hammer made of cast Fe–8Cr–2B alloy quenching from 1050 °C and tempering from 300 °C has good application effect, and its service life improves by 150–180% than that of high manganese steel hammer.     

One‐Step Transfer and Integration of Multifunctionality in CVD Graphene by TiO2/Graphene Oxide Hybrid Layer

We present a straightforward method for simultaneously enhancing the electrical conductivity, environmental stability, and photocatalytic properties of graphene films through one‐step transfer of CVD graphene and integration by introducing TiO₂/graphene oxide layer. A highly durable and flexible TiO₂ layer is successfully used as a supporting layer for graphene transfer instead of the commonly used PMMA. Transferred graphene/TiO₂ film is directly used for measuring the carrier transport and optoelectronic properties without an extra TiO₂ removal and following deposition steps for multifunctional integration into devices because the thin TiO₂ layer is optically transparent and electrically semiconducting. Moreover, the TiO₂ layer induces charge screening by electrostatically interacting with the residual oxygen moieties on graphene, which are charge scattering centers, resulting in a reduced current hysteresis. Adsorption of water and other chemical molecules onto the graphene surface is also prevented by the passivating TiO₂ layer, resulting in the long term environmental stability of the graphene under high temperature and humidity. In addition, the graphene/TiO₂ film shows effectively enhanced photocatalytic properties because of the increase in the transport efficiency of the photogenerated electrons due to the decrease in the injection barrier formed at the interface between the F‐doped tin oxide and TiO₂ layers.     

Effect of lead on formation and dielectric tunability of (Pbx,Sr1? x )0.85Bi0.1TiO3 thin films

(Pb_x,Sr_1−x )_0.85Bi_0.1TiO₃ thin films with the perovskite phase structure were prepared on an ITO glass substrate by sol-gel method. X-ray diffraction (XRD), scanning electron microscopy (SEM) and an impedance analyzer were respectively used in order to characterize the phase status, morphology and dielectric properties of the thin films. The results show that during the formation process of (Pb_x,Sr_1−x )_0.85Bi_0.1TiO₃ thin films, the nucleus of the perovskite phase are initially formed and then congregated. These aggregated nucleus are then transformed as the perovskite-phase crystalline in the thin film. Finally, the crystalline phase grows and separates gradually to form the perfect crystalline-phase structure. The content of the perovskite phase formed in the thin film under rapid thermal process (RTP) is more than that formed under traditional heat treatment with kinetic equilibrium. This is due to the high active decomposed ions that form the perovskite phase directly when heat-treated by RTP. The formation of the perovskite phase therefore overcomes a much lower barrier under RTP than that under traditional calcinations. The structure of the perovskite phase has a close relation to the ratio of Pb/Sr in the system because of the radius difference between Pb²⁺ and Sr²⁺. The transformation temperature between the cubic and the tetragonal structures of the perovskite phase increases with increasing Pb²⁺ content because the radius of Pb²⁺ is larger than that of Sr²⁺. It appears at room temperature when the content of Pb²⁺/Sr²⁺ is about 40/60 in the thin film. Meanwhile, the tetragonality of the perovskite phase is increased when Pb²⁺ ions increase due to its high polarization. The higher tunability of the (Pb_x,Sr_1−x )_0.85Bi_0.1TiO₃ thin film is exhibited when the film composition is close to the transformation point between the paraelectric and ferroelectric phases. Pb²⁺ ions show a dominant factor to affect the Curie point of the system and then changing tunability. Translated from Journal of Inorganic Materials, 2006, 21(2): 466–472 [译自: 无机材料学报]     

Pressure-driven reverse-phase liquid chromatography separations in ordered nonporous pillar array columns

Building upon the micromachined column idea proposed by the group of Regnier in 1998, we report on the first high-resolution reversed-phase separations in micromachined pillar array columns under pressure-driven LC conditions. A three component mixture could be separated in 3 s using arrays of nonporous silicon pillars with a diameter of approximately 4.3 microm and an external porosity of 55%. Under slightly retained component conditions (retention factor k' = 0.65-1.2), plate heights of about H = 4 microm were obtained at a mobile phase velocity around u = 0.5 mm/s. In reduced terms, such plate heights are as low as hmin = 1. Also, since the flow resistance of the column is much smaller than in a packed column (mainly because of the higher external porosity of the pillar array), the separation impedance of the array was as small as E = 150, i.e., of the same order as the best currently existing monolithic columns. At pH = 3, yielding very low retention factors (k' = 0.13 and 0.23), plate heights as low as H = 2 microm were realized, yielding a separation of the three component mixture with an efficiency of N = 4000-5000 plates over a column length of 1 cm. At higher retention factors, significantly larger plate heights were obtained. More experimental work is needed to investigate this more in depth. The study is completed with a discussion of the performance limits of the pillar array column concept in the frame of the current state-of-the-art in microfabrication precision.     

土-结构相互作用对储液结构动力反应的影响研究

在对大型工程结构进行地震反应分析时土-结构相互作用通常不可忽略,然而,结构本身巨大的体量及考虑土-结构相互作用后引入的大范围土域模型导致计算规模通常十分庞大,由此引起的计算效率低下问题已成为制约此类结构性能分析的关键因素。该文提出一种新型土-结相互作用分析方法,并基于此实现了大型结构考虑土-结构相互作用的高效地震反应分析,建立不同接触状态下的单元法向和剪切相对位移分解方法;采用三维无厚度Goodman接触面单元格式对土与结构的接触行为进行描述,并通过插值方法对单元非线性变形进行描述,推导出隔离非线性的接触面单元控制方程;在此基础上,建立了大型工程结构考虑土-结构相互作用的整体式计算模型和高效地震反应分析方法。由于该文方法在每次迭代求解过程采用Woodbury公式计算结构响应,其仅需对一个规模极小的局部非线性矩阵进行迭代更新,避免了传统方法所需的结构大规模整体刚度矩阵实时更新分解,因而能够大幅度提高结构地震反应分析效率,数值算例验证了该文方法的有效性及高效性。

     

Growth and spectral properties of Cr:KAl(MoO4)2 crystal

The Cr³⁺:KAl(MoO₄)₂ single crystal was grown by top seeding solution growth method (TSSG). Based on the absorption and emission spectra, the crystal field strength Dq, the Racah parameters B and C, the effective phonon energy ?ω and the Huang-Rhys factor S were calculated: Dq = 1494.8 cm^− 1, B = 585.5 cm^− 1 and C = 3049 cm^− 1, ?ω = 373.8 cm^− 1 and the Huang-Rhys factor S = 3.74, respectively. The value Dq/B = 2.55 indicates that Cr³⁺ ion occupies the strong crystal field site in KAl(MoO₄)₂ crystal. A comparison of crystal field parameters for Cr³⁺:KAl(MoO₄)₂ with other Cr³⁺-doped crystals was presented. The results of spectral measurement show that Cr³⁺:KAl(MoO₄)₂ may be a potential candidate for broadband laser applications.