有限元法模拟开挖引起的基坑水平位移和邻近建筑物沉降   总被引：1，自引：1，他引：0  

王晓  韦俊山  李巨龙  翟守俊 《上海国土资源》2008,(1):29-31,52

以徐州某采用水泥土墙支护的基坑为例,采用有限元数值模拟的方法,对基坑开挖引起的水平位移量和邻近建筑物沉降量进行了计算,并与实际监测值进行了对比分析,得到了一些关于如何控制基坑水平位移和减少基坑周边建筑沉降的结论。  相似文献   

上海市长江口及邻近海域地质调查现状及展望   总被引：1，自引：1，他引：0  

谢建磊  王寒梅  何中发  李晓  黎兵 《上海国土资源》2008,(4)

海洋区域地质调查近年来逐渐得到重视,海洋地质调查技术的发展也为开展海洋区域地质调查奠定了基础。上海地区社会经济发展对地质工作的需求,为摸清上海市长江口及邻近海域的地质现状提出了必然要求。本文在系统整理长江口及邻近海域地质资料的基础上,重点分析了区内存在的重点地质问题和研究存在的问题,根据海洋地质调查的技术发展,结合国内相关地区的调查经验,对长江口及邻近海域内区域地质调查进行了展望,提出了采用综合物探技术、地质取样和测试分析进行综合地质环境调查的建议,并对具体采用的调查技术和调查内容进行了论述。  相似文献   

贵州省大方县五凤井田水文地质特征初探     

向国灿 《中国煤炭地质》2008,20(4):49-52

五风井田位于贵州省大方县城东侧,面积89.22km^2,含煤地层为二叠系上统龙潭组,主要可采煤层为6中、26、33号煤层,煤炭总资源量26 130万t。井田内主要含水层为三叠系茅草铺组岩溶溶洞含水层（T1m）,夜郎组玉龙山灰岩岩溶裂隙含水层T1y2）,二叠系中统长兴组岩溶裂隙含水层（P3c）、茅口组岩溶溶洞-暗河含水层（P2m）。矿床属于以岩溶充水为主,水文地质条件中等的矿床。井田的充水水源为地表水、地下水和小煤矿、采空区的老窑积水,充水通道为断裂破碎带及采矿冒落裂隙带。  相似文献   

Propagation of MHD body and surface waves in magnetically structured regions of the solar atmosphere     

S. T. Wu  Y. C. Xiao  Z. E. Musielak  S. T. Suess 《Solar physics》1996,163(2):291-307

The fact that magnetically structured regions exist in the solar atmosphere has been known for a number of years. It has been suggested that different kinds of magnetohydrodynamic (MHD) waves can be efficiently damped in these regions and that the dissipated wave energy may be responsible for the observed enhancement in radiative losses. From a theoretical point of view, an important task would be to investigate the propagation and dissipation of MHD waves in these highly structured regions of the solar atmosphere. In this paper, we study the behavior of MHD body and surface waves in a medium with either a single or double (slab) magnetic interface by use of a nonlinear, two-dimensional, time-dependent, ideal MHD numerical model constructed on the basis of a Lagrangean grid and semi-implicit scheme. The processes of wave confinement and wave energy leakage are discussed in detail. It is shown that the obtained results depend strongly on the type of perturbations imposed on the interface or slab and on the plasma parameter, . The relevance of the obtained results to the heating problem of the upper parts of the solar atmosphere is also discussed.  相似文献   

生物炭对磷石膏中磷的固化作用     

敖翔  徐冠立  李珎  柏涵 《岩石矿物学杂志》2024,43(1):100-108

磷石膏中的磷在雨水淋滤作用下浸出,将污染堆场附近水体。本研究采用生物炭固化磷石膏中的磷,以减少其对周遭水体的污染。主要通过模拟固化实验和对照浸出实验,分析生物炭用量、反应时间和温度、初始pH值对固化效果的影响,通过XRD、SEM-EDS分析固化后的生成物。实验结果显示,在生物炭用量为25 mg时,单位固化量达到最大值13.20 mg/g;在反应温度T=293 K、初始pH=7条件下,反应平衡时间72 h时浸出液的磷平衡浓度C_e= 1.40 mg/L;温度提升有助于提高生物炭的固化效果,当T=308 K时,浸出液的磷平衡浓度C_e=0.167 mg/L;碱性条件有利于固化反应持续进行,在pH=11条件下,浸出液的磷平衡浓度C_e=0.153 mg/L。实验结果表明生物炭对磷石膏中的磷具有明显的固化效果。磷石膏中的二水硫酸钙溶解后,Ca²⁺与表面带负电的生物炭结合,在生物炭显微结构的凹陷处,化学吸附溶液中的磷酸根生成了絮状、团簇状的羟基磷灰石(HAP)沉淀,从而使浸出磷得到有效控制。  相似文献   

流体在岩浆型铬铁矿和铂族元素成矿过程中的作用及意义     

苏本勋  刘霞  袁庆晗  罗扬  潘旗旗  白洋  崔梦萌  肖燕  唐冬梅 《地质学报》2022,96(12):4091-4100

镁铁- 超镁铁岩是揭示地幔物质组成和壳幔相互作用的重要窗口，也是Ni- Cu- PGE- Cr等金属矿产资源的重要载体。不同的镁铁- 超镁铁岩体赋矿特征明显不同：蛇绿岩以产出铬铁矿床为特征，阿拉斯加型岩体主要赋含铂族元素(PGE)矿床，大型层状岩体则可同时产出铬铁矿床、PGE矿床和Cu- Ni硫化物矿床。这种成矿差异显然与赋矿岩体形成的构造背景、母岩浆经历的岩浆演化过程有关，但缺少关键控制因素的研究。前人对上述不同种类矿床的研究工作主要集中于地幔源区的部分熔融、上升过程中或岩浆房内的围岩混染和结晶分异等岩浆过程，而极少关注流体作用。近年来，实验岩石学和岩石地球化学的研究均表明幔源岩浆演化过程中的流体活动可能对成矿元素的富集迁移起到至关重要的作用，同时这些成矿元素的赋存状态和分配系数也在不断更新。厘清Cr和PGE在熔体演化——尤其是流体出溶过程中的地球化学行为，刻画并揭示其迁移富集、分离和再富集的成矿过程及控制因素，已成为当前岩浆矿床研究的热点。本文围绕富水流体与铬铁矿和PGE成矿关系的科学问题，总结了不同镁铁- 超镁铁岩体的成矿差异以及铬铁矿和PGE矿床成矿过程中的流体活动记录，提出流体性质和组分对铬铁矿和PGE迁移富集的控制作用，强调有必要开展蛇绿岩、大型层状镁铁- 超镁铁岩体和阿拉斯加型岩体的对比研究。  相似文献   

基于GIS城市洪水淹没模拟分析   总被引：10，自引：0，他引：10       下载免费PDF全文

向素玉  陈军 《地球科学》1995,20(5):575-580

城市洪水淹没范围动态模拟分析是城市防洪规划与防治决策的一个重要基础工作。本文主要研究洪水从翻堤口出发在地理空间蔓延、扩散、动态行进及确定淹没范围的数字模拟方法。为此,根据数学形态学及测地圆概念,研究设计了洪水扩散范围的“膨胀”模拟算法和淹没范围搜索算法,用于查询淹没通块中从翻堤处到任一点之间的淹没路径和ｔ时刻洪水扩散范围。  相似文献   

福州古桥文化资源特征、保护及开发利用初探     

郭唯  袁书琪  李晓 《亚热带资源与环境学报》2006,21(2):55-58

福州古桥素以技术精湛、构造独特、规模宏大以及雕刻细腻而闻名中外.古桥既凝聚了工匠们的劳动创造精神,又积淀了深厚的历史文化,极具学术、文物和旅游价值.目前福州古桥状况堪忧,本文在考察古桥现状特色的基础上,分析面临的问题,提出一些保护及开发利用的建议.  相似文献   

Na depletion in modern adakites via melt / rock reaction within the sub-arc mantle     

X.L. Xiong  B. Xia  J.F. Xu  H.C. Niu  W.S. Xiao 《Chemical Geology》2006,229(4):273-292

Interaction between slab-derived melt and mantle peridotite and the role of slab melt as a metasomatizing agent in the sub-arc mantle is being increasingly recognized. Adakite, the slab melt erupted on the surface, usually exhibits anomalously high MgO, CaO, Cr and Ni contents that indicate interaction with mantle peridotitite. Here we note that Cenozoic adakites have Na₂O contents below 5.8 wt.% with ∼95% samples lower than 5.0 wt.%, and are generally depleted in this component relative to experimental basalt partial melts (mostly beyond 5.0 wt.% and up to 9.0 wt.% Na₂O) produced under 1.5-3.0 GPa conditions that are most relevant to adakite production. We interpret the adakite Na depletion to be also a consequence of the melt / rock reaction that takes place within the hot mantle wedge. During ascent and reaction with mantle peridotite, primary adakite melts gain mantle components MgO, CaO, Cr and Ni but lose Na₂O, SiO₂ and perhaps K₂O to the mantle, leading to Na-rich mantle metasomatism. Selective assimilation of predominately mantle clinopyroxene, some spinel and minor olivine at high T/P has been considered to be an important process in producing high-Mg adakites from primary low-Mg slab melts [Killian, R., Stern, C. R., 2002. Constraints on the interaction between slab melts and the mantle wedge from adakitic glass in peridotite xenoliths. Eur. J. Mineral. 14, 25-36]. In such a process, Na depletion in the assimilated melt is the result of dilution due to the increase in melt mass. Phase relationships in the reaction system siliceous melt + peridotite and quantitative calculation suggest that assimilation of mantle clinopyroxene, olivine and spinel and fractional crystallization of sodic amphibole and orthopyroxene, under conditions of moderate T/P and increasing melt mass, is also an important process that modifies the composition of adakites and causes the Na depletion.  相似文献   

Cs and Cl NMR spectroscopy and molecular dynamics modeling of Cs and Cl complexation with natural organic matter     

Xiang Xu 《Geochimica et cosmochimica acta》2006,70(17):4319-4331

Interaction of dissolved aqueous species with natural organic matter (NOM) is thought to be important in sequestering some species and enhancing the transport of others, but little is known about these interactions on a molecular scale. This paper describes a combined experimental ¹³³Cs and ³⁵Cl nuclear magnetic resonance (NMR) and computational molecular dynamics (MD) modeling study of the interaction of Cs⁺ and Cl⁻ with Suwannee River NOM. The results provide a detailed picture of the molecular-scale structure and dynamics of these interactions. Individual NOM molecules are typically hundreds to thousands of Daltons in weight, and on the molecular scale their interaction with small dissolved species can be investigated in ways similar to those used to study the interaction of dissolved aqueous species with mineral surfaces. As for such surface interactions, understanding both the structural environments and the dynamics over a wide range of frequencies is essential. The NMR results show that Cs⁺ is associated with NOM at pH values from 3.4 ± 0.5 (unbuffered Suwannee River NOM solution) to 9.0 ± 0.5. The extent of interaction increases with decreasing CsCl concentration at constant pH. It also decreases with increasing pH at constant CsCl concentration due to pH-dependent negative structural charge development on the NOM caused by progressive deprotonation of carboxylic and phenolic groups. The presence of NOM has little effect on the ¹³³Cs chemical shifts, demonstrating that its local coordination environment does not change significantly due to interaction with the NOM. Narrow, solution-like line widths indicate rapid exchange of Cs⁺ between the NOM and bulk solution at frequencies of >10² Hz. The MD simulations support these results and show that Cs⁺ is associated with the NOM principally as outer sphere complexes and that this interaction does not reduce the Cs⁺ diffusion coefficient sufficiently to cause NMR line broadening. The ³⁵Cl NMR data and the MD results are consistent in demonstrating that there is no significant complexation between Cl⁻ and NOM in the pH range investigated, consistent with negative structural charge on the NOM.  相似文献