含气软黏土的不排水抗剪强度计算模型     

郑威威  洪义  王立忠 《岩土力学》2022,43(8):2233-2240

含气软黏土广泛分布在世界五大洲,大量离散气泡的存在对软黏土的不排水抗剪强度具有强化或损伤作用,然而目前仍缺乏能综合考虑气相强化与气相损伤竞争机制的含气土不排水剪切强度解析表达式。结合临界状态土力学理论,基于笔者提出的含气土屈服函数,建立了v-lnp¢ 空间下临界状态线截距与土体含气特性(u_{w 0},y₀)的数学关系,进而推导了含气软黏土在三轴应力状态下不排水抗剪强度s_u的理论显式表达式。同时,采用所提出的含气软黏土不排水抗剪强度理论计算公式,分别对比了3种典型的含气软黏土在不同含气特性下的不排水抗剪强度理论预测与试验结果,包括马来西亚高岭土、Combwich 黏土和高岭黏土。另外,对比分析了4种不同的含气软黏土不排水抗剪强度理论计算模型的预测误差百分比,证明了提出的基于改进的含气软黏土本构模型的不排水抗剪强度理论计算式的合理性,能够更加准确地同时考虑含气软黏土的气相强化与气相损伤双重效应。  相似文献   

导航卫星天线相位中心误差标定方法研究现状及发展趋势   总被引：1，自引：0，他引：1  

刘伟平  郝金明  邓科 《测绘通报》2018,(3):1-8

卫星天线相位中心误差是影响GNSS高精度定位定轨的重要误差源,实用中需要对其精确标定。随着北斗卫星导航系统的建设发展,如何对卫星天线相位中心误差进行更为精确的标定应引起人们的重视。为此,本文首先简要介绍了各卫星导航系统的卫星天线情况,而后系统总结了导航卫星天线相位中心误差标定方法的发展历程和研究现状,指出了未来卫星天线相位中心误差标定方法的发展趋势,相关研究成果对我国北斗卫星天线相位中心误差的标定方法研究具有参考意义。  相似文献   

济南泉域地下水位动态及其对降水响应的交叉小波分析   总被引：8，自引：0，他引：8  

祁晓凡  杨丽芝  韩晔  尚浩  邢立亭 《地球科学进展》2012,27(9):969-978

利用1988—2009年济南泉域8个地下水位动态观测点不同时段观测资料及1998—2009年降水数据,采用连续小波变换、交叉小波变换方法对济南泉域地下水位动态的多时间尺度特征、相互关系及其对降水的响应进行了分析。结果表明:①济南泉域地下水位动态存在显著的0.82～1.16 a的主振荡周期,低频部分仅在部分年份存在1.95～3.09 a的振荡周期;②含水岩组富水性对地下水位动态存在影响,研究区主径流方向上弱富水性地段地下水位动态时滞较强富水性地段长,强富水性地段4个观测孔地下水位波动时序基本一致;③地下水位动态对降水的响应滞后明显,为73.06～134.42 d,总体表现为地下水径流路径越长,响应越滞后;④基于地下水位动态与基于降水—地下水位动态交叉小波变换得到的观测点对水位动态的滞后时间多数一致,同一径流路径上局部点对滞后时间之和与全局点对有很好的对应关系。交叉小波分析可定量评价泉域地下水位动态及其与降水的相关关系。  相似文献   

成庄矿区构造特征及应力场分析     

王彦军  赵学晶 《安徽地质》2012,(2):93-97,102

本文对成庄矿区褶皱、断层及3号煤层的构造特征进行了总结论述.通过对矿区节理的统计、配套和分期,对该区燕山期以来的主应力方位、期次进行了划分,将主应力划分为3期,同时将成庄矿区含煤地层形成以后的构造演化划分为三个阶段:早期应力阶段奠定成庄矿区煤田构造基本格架;中期应力阶段对成庄矿区造成的影响很小;晚期应力阶段完成了矿区内煤田构造基本格局.  相似文献   

一种基于相位的相对延迟变化测量方法     

王锦清  韦文仁 《中国科学院上海天文台年刊》2007,(1):119-127

详细地介绍了VLBI系统的地面单元中电缆延迟变化的测量方法，这种基于相位的测量方法，为相关领域的高精度延迟测量提供了借鉴。概要介绍了地面单元中电缆测量、反射调制以及相位比较器的工作原理，对各个环节作了数学上的推导分析。给出了一个电缆相对延迟值随温度变化的测试样本。  相似文献   

Chloritoid–glaucophane schist in the north Qilian orogen, NW China: phase equilibria and P–T path from garnet zonation     

C. J. WEI  S. G. SONG 《Journal of Metamorphic Geology》2008,26(3):301-316

Chloritoid–glaucophane‐bearing rocks are widespread in the high‐pressure belt of the north Qilian orogen, NW China. They are interbedded and cofacial with felsic schists originated from greywackes, mafic garnet blueschists and low‐T eclogites. Two representative chloritoid–glaucophane‐bearing assemblages are chloritoid + glaucophane + garnet + talc + quartz (sample Q5‐49) and chloritoid + glaucophane + garnet + phengite + epidote + quartz (sample Q5‐12). Garnet in sample Q5‐49 is coarse‐, medium‐ and fine‐grained and shows two types of zonation patterns. In pattern I, X_grs is constant as X_py rises, and in pattern II X_grs decreases as X_py rises. Phase equilibrium modelling in the NC(K)MnFMASH system with Thermocalc 3.25 indicates that pattern I can be formed during progressive metamorphism in lawsonite‐stable assemblages, while pattern II zonation can be formed with further heating after lawsonite has been consumed. Garnet growth in Q5‐49 is consistent with a continuous progressive metamorphic process from ～14.5 kbar at 470 °C to ～22.5 kbar at 560 °C. Garnet in sample Q5‐12 develops with pattern I zonation, which is consistent with a progressive metamorphic process from ～21 kbar at 540 °C to ～23.5 kbar at 580 °C with lawsonite present in the whole garnet growth. The latter sample shows the highest P–T conditions of the reported chloritoid–glaucophane‐bearing assemblages. Phase equilibrium calculation in the NCKFMASH system with a recent mixing model of amphibole indicates that chloritoid + glaucophane paragenesis does not have a low‐pressure limit of 18–19 kbar as previously suggested, but has a much larger pressure range from 7–8 to 27–30 kbar, with the low‐pressure part being within the stability field of albite.  相似文献   

Constraining peak P–T conditions in UHP eclogites: calculated phase equilibria in kyanite‐ and phengite‐bearing eclogite of the Tromsø Nappe,Norway     

M. JANÁK  E. J. K. RAVNA  K. KULLERUD 《Journal of Metamorphic Geology》2012,30(4):377-396

Kyanite‐ and phengite‐bearing eclogites have better potential to constrain the peak metamorphic P–T conditions from phase equilibria between garnet + omphacite + kyanite + phengite + quartz/coesite than common, mostly bimineralic (garnet + omphacite) eclogites, as exemplified by this study. Textural relationships, conventional geothermobarometry and thermodynamic modelling have been used to constrain the metamorphic evolution of the Tromsdalstind eclogite from the Tromsø Nappe, one of the biggest exposures of eclogite in the Scandinavian Caledonides. The phase relationships demonstrate that the rock progressively dehydrated, resulting in breakdown of amphibole and zoisite at increasing pressure. The peak‐pressure mineral assemblage was garnet + omphacite + kyanite + phengite + coesite, inferred from polycrystalline quartz included in radially fractured omphacite. This omphacite, with up to 37 mol.% of jadeite and 3% of the Ca‐Eskola component, contains oriented rods of silica composition. Garnet shows higher grossular (X_Grs = 0.25–0.29), but lower pyrope‐content (X_Prp = 0. 37–0.39) in the core than the rim, while phengite contains up to 3.5 Si pfu. The compositional isopleths for garnet core, phengite and omphacite constrain the P–T conditions to 3.2–3.5 GPa and 720–800 °C, in good agreement with the results obtained from conventional geothermobarometry (3.2–3.5 GPa & 730–780 °C). Peak‐pressure assemblage is variably overprinted by symplectites of diopside + plagioclase after omphacite, biotite and plagioclase after phengite, and sapphirine + spinel + corundum + plagioclase after kyanite. Exhumation from ultrahigh‐pressure (UHP) conditions to 1.3–1.5 GPa at 740–770 °C is constrained by the garnet rim (X_Ca^Grt = 0.18–0.21) and symplectite clinopyroxene (X_Na^Cpx = 0.13–0.21), and to 0.5–0.7 GPa at 700–800 °C by sapphirine (X_Mg = 0.86–0.87) and spinel (X_Mg = 0.60–0.62) compositional isopleths. UHP metamorphism in the Tromsø Nappe is more widespread than previously known. Available data suggest that UHP eclogites were uplifted to lower crustal levels rapidly, within a short time interval (452–449 Ma) prior to the Scandian collision between Laurentia and Baltica. The Tromsø Nappe as the highest tectonic unit of the North Norwegian Caledonides is considered to be of Laurentian origin and UHP metamorphism could have resulted from subduction along the Laurentian continental margin. An alternative is that the Tromsø Nappe belonged to a continental margin of Baltica, which had already been subducted before the terminal Scandian collision, and was emplaced as an out‐of‐sequence thrust during the Scandian lateral transport of nappes.  相似文献   

An enlarged and updated internally consistent thermodynamic dataset with uncertainties and correlations: the system K2O–Na2O–CaO–MgO–MnO–FeO–Fe2O3–Al2O3–TiO2–SiO2–C–H2–O2     

T. J. B. HOLLAND  R. POWELL 《Journal of Metamorphic Geology》1990,8(1):89-124

We present, as a progress report, a revised and much enlarged version of the thermodynamic dataset given earlier (Holland & Powell, 1985). This new set includes data for 123 mineral and fluid end-members made consistent with over 200 P–T–X_CO2–f_O2 phase equilibrium experiments. Several improvements and advances have been made, in addition to the increased coverage of mineral phases: the data are now presented in three groups ranked according to reliability; a large number of iron-bearing phases has been included through experimental and, in some cases, natural Fe:Mg partitioning data; H₂O and CO₂ contents of cordierites are accounted for with the solution model of Kurepin (1985); simple Landau theory is used to model lambda anomalies in heat capacity and the Al/Si order–disorder behaviour in some silicates, and Tschermak-substituted end-members have been derived for iron and magnesium end-members of chlorite, talc, muscovite, biotite, pyroxene and amphibole. For the subset of data which overlap those of Berman (1988), it is encouraging to find both (1) very substantial agreement between the two sets of thermodynamic data and (2) that the two sets reproduce the phase equilibrium experimental brackets to a very similar degree of accuracy. The main differences in the two datasets involve size (123 as compared to 67 end-members), the methods used in data reduction (least squares as compared to linear programming), and the provision for estimation of uncertainties with this dataset. For calculations on mineral assemblages in rocks, we aim to maximize the information available from the dataset, by combining the equilibria from all the reactions which can be written between the end-members in the minerals. For phase diagram calculations, we calculate the compositions of complex solid solutions (together with P and T) involved in invariant, univariant and divariant assemblages. Moreover we strongly believe in attempting to assess the probable uncertainties in calculated equilibria and hence provide a framework for performing simple error propagation in all calculations in thermocalc, the computer program we offer for an effective use of the dataset and the calculation methods we advocate.  相似文献   

基于小波变换的周跳探测与修复   总被引：2，自引：1，他引：1  

张金华  胡伍生 《测绘工程》2009,18(4):24-27

探测和修复周跳一直是GPS定位中的关键问题。利用小波变换对相位减伪距观测量进行周跳探测。首先介绍小波变换周跳探测的一般方法，然后在此基础上提出改进。改进方法可以对周跳进行探测和直接修复，进而探测和修复多次周跳，同时有效地克服一般方法可能出现探测失误的缺点。这种改进方法的效果在实验中得到验证。  相似文献   

A new method for the quantification of different redox-species of molybdenum (V and VI) in seawater   总被引：1，自引：0，他引：1  

Deli Wang  Robert C. Aller  Sergio A. Saudo-Wilhelmy 《Marine Chemistry》2009,113(3-4):250-256

A new method for the direct determination of reduced and oxidized Mo species (Mo (V) and Mo (VI)) in seawater was developed and used for the first time. The method includes the complexation of Mo (V) with tartrate, solid phase extraction of the Mo (V)–tartrate complex by a XAD 7HP resin, followed by elution with acidic acetone. In this study, the eluted Mo (V) was quantified by graphite furnace atomic absorption spectrometry. The detection limit of this protocol was on the order of 0.2 nM. The analytical precision was 10% of ~ 10 nM. This method was successfully applied to the determination of Mo (V) and Mo (VI) in surface and bottom waters at the head of Peconic River Estuary. Total Mo (Mo (V) + Mo (VI)) ranged from 100–120 nM in most bottom saline waters, and 2.5–15 nM for surface fresher waters. Concentrations of Mo (V) in these environments ranged from 0 nM to ~ 15 nM, accounting for 0%–15% of the total dissolved Mo pool. The time series experiments showed that the Mo speciation changed within 1 h after the water collection, and therefore it is strongly suggested that speciation analysis be carried out within the first 15 min. However, since these are the first Mo speciation data in concentration ranges typical of normal marine and coastal waters, additional research may be required to optimize the methodology and further explore Mo cycling mechanisms.  相似文献