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941.
水库滑坡位移与水动力耦合预测参数及其评价方法研究 总被引:2,自引:0,他引:2
针对库水涨落诱发滑坡致灾机理,在系统分析水库边坡位移与库水位变化规律及其相互作用关系的基础上,运用弹塑性力学基本原理,提出了以库水位下降引起的边坡下滑动力增量作为边坡的加载动力参数,以相应边坡位移变化量作为边坡位移响应参数,以此确定水库边坡库水动力增载位移响应比参数并建立预测模型。运用动力增载位移响应比预测模型对三峡库区典型水库滑坡-黄土坡滑坡关键部位监测点进行了动力增载位移响应比计算,并采用Geostudio软件对该滑坡稳定性进行了数值模拟分析。该滑坡的位移响应特征与稳定性演化规律表明,该滑坡关键变形部位的动力增载位移响应比参数变化规律与其实际位移与稳定性演化规律基本吻合。研究结果表明了动力增载位移响应比参数是水库滑坡有效的位移动力评价参数,可运用该参数及其评价方法对水库滑坡进行稳定性分析与评价。 相似文献
942.
By means of the molecular dynamics (MD) simulation, the crystallization mechanism of 22,8-polyurethane which contains hydrogen-bond units is investigated and the results show that the crystallization process at a fixed temperature can be characterized by three stages: (1) The extended chain collapses to a globular random coil; (2) The random coil reorganizes into an ordered lamellar structure; (3) Accompanied with the segments clustering due to the hydrogen-bond formation, the lamellar develops with local defects. Two kinds of hydrogen-bond, which are formed between NH group and CO group (N-H?OC), and between NH group and urethane alkoxy oxygen (N-H?O), respectively, are found to play an important role in the crystallization process of 22,8-polyurethane. Furthermore, the effect of temperature on the crystallization is also studied by selecting three temperatures 200, 300 and 400 K. The lower the crystal temperature is, the slower the crystallization rate is and the stronger the hydrogen-bonding interactions are presented. This is in harmony with the experimental results. 相似文献
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The morphology and mechanical properties of PVC/SMA‐g‐PA6 blends were investigated in this paper. Graft to polymer SMA‐g‐PA6 was prepared via a solution graft reaction between SMA and PA6. FTIR test evidences the occurrence of the graft reaction between SMA and PA6. DSC analysis shows that SMA‐g‐PA6 has a lower melting point of 187°C, which may result in a decrease in crystallinity of PA6 and thus enable efficient blending of SMA‐g‐PA6 and PVC. Compatibilization was evidenced by the dramatic increase in mechanical properties, the smaller particle size and finer dispersion of PA6 in PVC matrix, and, further, a cocontinuous morphology at 16 wt % SMA‐g‐PA6 content. SMA‐g‐PA6 from the solution graft reaction can toughen and reinforce PVC material. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 432–439, 2004 相似文献
947.
Boron-based metal-free catalysts for oxidative dehydrogenation of propane (ODHP) have drawn great attention in both academia and industry due to their impressive activity and olefin selectivity. Herein, the SiO2 and B2O3 sequentially coated honeycomb cordierite catalyst is designed by a two-step wash-coat method with different B2O3 loadings (0.1%–10%) and calcination temperatures (600, 700, 800 °C). SiO2 obtained by TEOS hydrolysis acts as a media layer to bridge the cordierite substrate and boron oxide via abundant SiOH groups. The well-developed straight channels of honeycomb cordierite make it possible to carry out the reactor under high gas hourly space velocity (GHSV) and the thin wash-coated B2O3 layer can effectively facilitate the pore diffusion on the catalyst. The prepared B2O3/SiO2@HC monolithic catalyst exhibits good catalytic performance at low boron oxide loading and achieves excellent propylene selectivity (86.0%), olefin selectivity (97.6%, propylene and ethylene) and negligible CO2 (0.1%) at 16.9% propane conversion under high GHSV of 345,600 ml·(g B2O3)−1·h−1, leading to a high propylene space time yield of 15.7 g C3H6·(g B2O3)−1·h−1 by suppressing the overoxidation. The obtained results strongly indicate that the boron-based monolithic catalyst can be properly fabricated to warrant the high activity and high throughput with its high gas/surface ratio and straight channels. 相似文献
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