共查询到20条相似文献，搜索用时 93 毫秒
1.
本文简单介绍了沈阳外环高速公路监控电缆非开挖铺设工程施工工艺的确定,施工设备的研制和施工过程,探讨了气动潜孔冲击器在砂卵石地层施工的优势,介绍在砂卵石地层中用非开挖铺设小于２００ｍｍ直径管道的新型施工工具和配备机具。 相似文献
2.
U型渠在土地整理项目的农田水利工程中较常见，使用范围较广。就U型渠工程施工步骤、施工测量控制、土方开挖与回填、垫层铺设、U型槽铺设等施工过程及其技术要求进行初步探讨。 相似文献
3.
4.
非开挖技术在市政管道铺设中的应用越来越广泛,从直径50mm通讯光缆-直径3000mm混凝土管道,采用非开挖安装各种管道都变得很普遍。同时,鉴于非开挖技术综合效益优越性、环境友好型施工特点,也逐渐被工程建设方、社会所接受和认可。泥水平衡顶管技术是非开挖最为成熟的技术之一,在城市市政设施建设中也起着举足轻重的作用。采用泥水平衡顶管技术进行城市雨污分流改造已经在国内大量城市取得应用,但是,采用泥水平衡顶管在岩层中铺设直径达2000mm埋深在5m电力管道,在国内为数不多,在福建厦门地区也是尚属首次。通过在工程施工中对设备、施工工艺的摸索和改进,最后采用泥水平衡顶管施工技术成功铺设建设方所要求的电力管道。本工程将为在福建地区采用预管技术铺设大口径长距离、曲线管道提供了指导和借鉴。 相似文献
5.
用非开挖导向钻进管线铺设技术,在河北省廊坊市广阳区陈桑园村完成了一浅层水平水井的施工,详尽介绍了该水平井施工方法及施工工艺。 相似文献
6.
非开挖技术在市政管道铺设中的应用越来越广泛,从直径50mm通讯光缆到直径3000mm混凝土管道,采用非开挖安装各种管道都变得很普遍。同时,鉴于非开挖技术综合效益优越性、环境友好型施工特点,也逐渐被工程建设方、社会所接受和认可。泥水平衡顶管技术是非开挖最为成熟的技术之一,在城市市政设施建设中也起着举足轻重的作用。采用泥水平衡顶管技术进行城市雨污分流改造已经在国内大量城市取得应用,但是,采用泥水平衡顶管在岩层中铺设直径迭2000mm埋深在5m电力管道,在国内为数不多,在福建厦门地区也是尚属首次。通过在工程施工中对设备、施工工艺的摸索和改进,最后采用泥水平衡顶管施工技术成功铺设建设方所要求的电力管道。本工程将为在福建地区采用顶管技术铺设大口径长距离、曲线管道提供了指导和借鉴。 相似文献
7.
8.
9.
10.
11.
The watershed in the southern Jiangxi Province (Jiangxi Province is called simply Gan) (SGW) and the watershed in the central Guizhou Province (Guizhou Province is called simply Qian) (CQW) are two subtropical watersheds of the Yangtze River in China. Both watersheds have similar latitudes and climate, but distinct differences in basin lithology. These similarities and differences provide a good natural laboratory in which to investigate weathering processes and Sr end-members in river waters. This work aims to identify and contrast the sources, fluxes and controls on Sr isotopic composition in the river waters of these two areas. Results showed that the 87Sr/86Sr in the SGW waters ranged from 0.716501 to 0.724931, with dissolved Sr averaging 27 μg l− 1. Rhyolites and granites are two major sources for the dissolved Sr. The SGW waters receive 42% of their Sr from silicates weathering, 32% from carbonates and 3.2% from evaporites. 87Sr/86Sr in the CQW waters has a lesser variation from 0.707694 to 0.710039, but higher Sr contents (average of 208 μg l− 1). Dolomite, limestone and dolomitic limestone are major sources of Sr in the waters. The CQW waters receive 69% of their Sr from carbonates, 1.7% from silicates and 0.9% from evaporites. The chemical erosion rate and Sr flux in the CQW are 122 t km− 2 a− 1 and 0.079 t km− 2 a− 1, respectively, which are higher than those of the SGW (56 t km− 2 a− 1 and 0.021 t km− 2 a− 1, respectively). These data suggest that the intensive carbonates weathering occurred in the karstic area in the upper-reach of the Yangtze River exert great influence on the high Sr concentration and low Sr isotopic ratios in the River. 相似文献
12.
Indigofera melanadenia and Tephrosia longipes plant species, collected from Cu–Ni mining area, were evaluated for accumulation of Cu and Ni. The total and bioavailable concentrations of Cu and Ni in the host soils were also determined. Flame Atomic Absorption Spectrometry was used for all metal determinations. The total and bioavailable concentrations of Cu in the soils were in the range 900–9000 μg/g and 200–2000 μg/g respectively. For Ni, the total and bioavailable concentrations were in the range 900–2000 μg/g and ∼ 40–100 μg/g respectively. The concentrations of Cu and Ni in the leaves of I. melanadenia were higher than in the roots with a range 80–130 μg/g in the leaves and 20–80 μg/g in the roots for Cu and a range of 150–200 μg/g in the leaves and 20–60 μg/g in the roots for Ni. Concentration of Cu in T. longipes was in the range of 37–240 μg/g and 150–200 μg/g in the leaves and roots respectively while the concentration of Ni was 80–140 μg/g in the leaves and 25–100 μg/g in the roots. Results indicate that both species have a potential for accumulating Cu and Ni. Translocation factor, a ratio of shoots to roots metal concentration, was used to evaluate the translocation properties of the plants from roots to shoots. Translocation factors of the plants were ≥ 1 suggesting efficient translocation of metals from roots to shoots. 相似文献
13.
Thermodynamic study of the association and separation of copper and gold in the Shizishan ore field, Tongling, Anhui Province, China 总被引：1，自引：0，他引：1
Xiao-chun Xu Zan-zan Zhang Qi-neng Liu Jing-wei Lou Qiao-qin Xie Ping-li Chu Ray L. Frost 《Ore Geology Reviews》2011,43(1):347-358
The Shizishan ore field is the largest gold–copper ore field in the Tongling ore district of Anhui Province, China. Copper and gold deposits in the district are present as one-commodity deposits or as deposits with both commodities. Copper and gold mineralization are either cogenetic or are temporally and spatially distinct. We present the results of systematic geochemical analysis of fluid inclusions from typical Au–Cu deposits in the Shizishan ore field; these data are used to determine the solubility of Cu and Au in the ore-forming fluids and to ascertain the mechanisms and factors that controlled variations in the association and separation of copper and gold mineralization. Our results indicate that copper in the ore-forming fluids was transported as CuCl2− and CuCl0 complexes and that the solubility of copper was controlled by variations in Cl− concentration. In addition, the precipitation of copper was controlled by changes in temperature, pH, fO2, and fO2. In comparison, gold in the ore-forming fluids was transported as Au(HS)2− and Au2S(HS)22− complexes, and the solubility of gold was controlled by variations in total sulfur concentration; the precipitation of gold was controlled by temperature, pH, fO2, and fO2. These differences between the two elements meant that copper and gold in the ore-forming fluids responded in different ways to changes in physicochemical conditions. Copper precipitated under relatively acidic conditions at high temperatures, while gold precipitated under weakly alkaline conditions at relatively low temperatures; this dissociation resulted in the temporal and spatial separation and zonation of copper and gold mineralization in the Shizishan ore field. 相似文献
14.
S. Quartieri G. Antonioli C. A. Geiger G. Artioli P. P. Lottici 《Physics and Chemistry of Minerals》1999,26(3):251-256
The incorporation and site preference of minor amounts (about 1 wt%) of Yb3+ in synthetic pyrope (Mg3Al2Si3O12) and grossular (Ca3Al2Si3O12) garnet were studied by X-ray Absorption Fine-Structure (XAFS) Spectroscopy. The measurements, performed in the temperature
range 77–343 K at both Yb LI- and LIII-edges, demonstrate that Yb3+ enters the garnet structure and is located in the dodecahedral site in both samples. The coordination environment of Yb3+ in the two samples was compared to that of the X-site cation in end-member synthetic pyrope and grossular and in Yb3Al5O12 as determined by single-crystal X-ray diffraction. The local geometry around Yb3+ is different from that of Mg and Ca in the bulk of the garnet, and also from that of Yb3+ in Yb3Al5O12.
Τhe XAFS results indicate that, (1) structural relaxation occurs around Yb3+ in the garnet structure; (2) the host garnet matrix exerts a major structural control on the incorporation of Yb3+, and (3) minor amounts of Yb3+ in garnet are located in structural sites and not in ill-defined defects.
Received: 15 January 1998/ Revised, accepted: 21 July 1998 相似文献
15.
Major and trace elements in groundwater from basaltic aquifers in pristine conditions were investigated in a volcanic island to evaluate sources, sinks, and mobility of elements over a wide range of mineralization conditions with total dissolved solids from 50 mg/L to 3400 mg/L. Groundwater was highly undersaturated with respect to primary silicate minerals, indicating that dissolution of basaltic rocks may continue under conditions with precipitation of calcite and secondary silicates. Evolution of B/Cl ratio in groundwater from marine aerosols to basaltic rocks showed that the ratio could be used as a conservative tracer for interactions between water and basaltic rocks. Relative mobility (RM) of elements calculated using the concentrations of elements in the local basaltic rocks and those in groundwater showed that mobility decreased in the order of B > Rb > Na > K > Mg > Ca > Mo > V > Si > Sr > Sc > P > U > Zn > Pb > Cr > Cu > Ba > Ni > Ti > (Mn, Al, Fe, Co, Th) indicating that oxyanion-forming elements and alkali metals had the highest mobility. Compared to average RM, V had decreased mobility, and Fe and Mn had increased mobility in anoxic groundwater while V, Mo, and U had higher mobility in oxic-alkaline water. The sources of V, Cr, Cu, and Zn in rocks were estimated using the partition coefficients between minerals and basaltic melt, and the disparity between sources and mobility indicated that sinks are more important for controlling the concentrations of these elements in groundwater than the contents in the rocks. Principal component analysis (PCA) of hydrogeochemical parameters in groundwater produced three principal components (PC) which represent dissolution of basaltic rocks without significant attenuation of released solutes, higher degree of water–rock interactions resulting in oxic-alkaline conditions, and attenuation of Zn and Cu in higher pH, respectively. Spatial distribution of PCs revealed that groundwater with elevated concentrations of mobile elements was concentrated in the southwestern area and that concentrations of V and Cr were more scattered, which is likely to be controlled by pH and redox states of groundwater as well as degree of water–rock interactions. 相似文献
16.
V. P. Solntsev R. I. Mashkovtsev A. V. Davydov E. G. Tsvetkov 《Physics and Chemistry of Minerals》2008,35(6):311-320
It is shown the possibility to determine the coordination of paramagnetic ions in disordered solid structures, e.g., in barium
borate glasses. For this purpose the electron paramagnetic resonance (EPR) method was used to study α-and β-BaB2O4 crystals and glasses of 45·BaO × 55·B2O3 and 40·BaO × 60·B2O3 (mol%) composition activated by Ag+ and Pb2+ ions. After the samples were exposed to X-rays at 77 K, different EPR centers were observed in them. In α-and β-BaB2O4 crystals and glasses the EPR centers Ag2+, Ag0, Pb+, Pb3+, and hole centers of O− type were studied. The EPR parameters of these centers and their arrangement in crystal structure were determined. It is
shown that Pb3+ ions in β-BaB2O4 crystals occupy Ba2+ position in an irregular polyhedron from the eight oxygen, whereas in α-BaB2O4 crystals they occupy Bа2 position in a sixfold coordination. Pb+ ions in α-BaB2O4 crystals occupy Bа1 position in a ninefold coordination from oxygen. In barium borate glasses, Pb3+ ions were studied in coordination polyhedron from six oxygen atoms and in a polyhedron from nine to ten oxygen atoms. It
is assumed that the established difference in the structural position of Pb3+ ions in glasses is due to their previous incorporation in associative cation–anion complexes (AC) and “free” structure-forming
cations (FC). Computer simulations have been performed to analyze the stability of specific associative complexes and to compare
their bond lengths with experimental data. 相似文献
17.
Heidy M. E. Van Kaam-Peters Stefan Schouten Jan W. De Leeuw Jaap S. Sinninghe Damst 《Organic Geochemistry》1997,27(7-8)
Structures and carbon isotopic compositions of biomarkers and kerogen pyrolysis products of a dolomite, a bituminous shale and an oil shale of the Kimmeridge Clay Formation (KCF) in Dorset were studied in order to gain insight into (i) the type and extent of water column anoxia and (ii) changes in the concentration and isotopic composition of dissolved inorganic carbon (DIC) in the palaeowater column. The samples studied fit into the curve of increasing δ13C of the kerogen (δ13CTOC) with increasing TOC, reported by Huc et al. (1992). Their hypothesis, that the positive correlation between TOC and δ13CTOC is the result of differing degrees of organic matter (OM) mineralisation in the water column, was tested by measuring the δ13C values of primary production markers. These δ13C values were found to differ on average by only 1‰ among the samples, implying that differences in the extent of OM mineralisation cannot fully account for the 3‰ difference in δ13CTOC. The extractable OM in the oil shale differs from that in the other sediments due to both differences in maturity, and differences in the planktonic community. These differences, however, are not likely to have significantly influenced δ13CTOC either. All three sediments contain abundant derivatives of isorenieratene, indicating that periodically euxinia was extending into the photic zone. The sediments are rich in organic sulfur, as revealed by the abundant sulfur compounds in the pyrolysates. The prominence of C1-C3 alkylated thiophenes over n-alkanes and n-alkenes is most pronounced in the pyrolysate of the sediment richest in TOC. This suggests that sulfurisation of OM may have played an important role in determining the TOC-δ13CTOC relationship reported by Huc et al. (1992). 相似文献
18.
E. Molinaroli S. Guerzoni G. De Falco A. Sarretta A. Cucco S. Como S. Simeone A. Perilli P. Magni 《Sedimentary Geology》2009,219(1-4):196-207
A comparison was made of shallow water sediments from the Lagoon of Venice (LV) and the Lagoon of Cabras (LC), comparing depositional environments and exploring the relationships between hydrodynamics and sedimentological parameters. The two water bodies are very different in size (LV: 360 km2; LC: 22 km2), and the sediments predominantly consist of silty-clay (LV: Mz ≈ 26 μm; LC: Mz ≈ 6 μm). However, there are large differences between the two lagoons with respect to sand (LV: mean 19%; LC: mean ~ 3%) and clay (LV: mean 20%; LC: mean 45%) contents. The Lagoon of Venice (mean depth ~ 1 m) can be considered a tidal basin, whereas the Lagoon of Cabras (mean depth ~ 2 m) has the character of a coastal lake in which wind is the main hydrodynamic forcing factor. A comparison of sediment grain-size distributions with water circulation patterns in different parts of the lagoons highlighted some interesting differences. Grain-size analyses of samples reveal a deficiency of particles around 8 μm in the LC, which is interpreted as reflecting the transition between cohesive flocs/aggregates and non-cohesive coarser silt particles, while the transition limit in the LV is ~ 20 μm. Thus, particles are cohesive below 8 μm in the LC and below ~ 20 μm in the LV. This is probably because of the differences in the clay/silt ratio, which is much lower in the LV (~ 0.3) than in LC (~ 1), conferring a “silt-dominated network structure” on most of the LV sediments.The hydrographical data used were root mean square velocity (RMSV) and water residence time (WRT), computed under the main forcing conditions. The results show a general correlation between RMSV and sortable silt in the LC, and between RMSV and coarser sediments (63–105 μm) in the LV. Some significant differences between the lagoons were detected in the degree of correlation between WRT and grain size. Root mean square velocity (~ 7 cm s− 1 in the LV and ~ 3 cm s− 1 in the LC) was a greater forcing factor in the LC than in the LV. Conversely, WRT, which is on average ~ 16 days in the LV and ~ 19 days in the LC, has more influence in the LV. This study highlights the usefulness of comparing environments with different hydrodynamic energies, e.g., tidal and/or wind-driven currents, to elucidate and thereby improve our understanding of the processes governing the spatial distribution of sedimentological features, the transport mechanisms of sediments, and the relationship between them. The results demonstrate that the approach outlined in this study has the potential to provide a universal hydro-sedimentological classification scheme. 相似文献
19.
U. Burenjargal A. Okamoto T. Kuwatani S. Sakata T. Hirata N. Tsuchiya 《Journal of Metamorphic Geology》2014,32(7):765-790
The timing and thermal effects of granitoid intrusions into accreted sedimentary rocks are important for understanding the growth process of continental crust. In this study, the petrology and geochronology of pelitic gneisses in the Tseel area of the Tseel terrane, SW Mongolia, are examined to understand the relationship between igneous activity and metamorphism during crustal evolution in the Central Asian Orogenic Belt (CAOB). Four mineral zones are recognized on the basis of progressive changes in the mineral assemblages in the pelitic gneisses, namely: the garnet, staurolite, sillimanite and cordierite zones. The gneisses with high metamorphic grades (i.e. sillimanite and cordierite zones) occur in the central part of the Tseel area, where granitoids are abundant. To the north and south of these granitoids, the metamorphic grade shows a gradual decrease. The composition of garnet in the pelitic gneisses varies systematically across the mineral zones, from grossular‐rich garnet in the garnet zone to zoned garnet with grossular‐rich cores and pyrope‐rich rims in the staurolite zone, and pyrope‐rich garnet in the sillimanite and cordierite zones. Thermobarometric analyses of individual garnet crystals reveal two main stages of metamorphism: (i) a high‐P and low‐T stage (as recorded by garnet in the garnet zone and garnet cores in the staurolite zone) at 520–580 °C and 4.5–7 kbar in the kyanite stability field and (ii) a low‐P and high‐T stage (garnet rims in the staurolite zone and garnet in the sillimanite and cordierite zones) at 570–680 °C and 3.0–6.0 kbar in the sillimanite stability field. The earlier high‐P metamorphism resulted in the growth of kyanite in quartz veins within the staurolite and sillimanite zones. The U–Pb zircon ages of pelitic gneisses and granitoids reveal that (i) the protolith (igneous) age of the pelitic gneisses is c. 510 Ma; (ii) the low‐P and high‐T metamorphism occurred at 377 ± 30 Ma; and (iii) this metamorphic stage was coeval with granitoid intrusion at 385 ± 7 Ma. The age of the earlier low‐T and high‐P metamorphism is not clearly recorded in the zircon, but probably corresponds to small age peaks at 450–400 Ma. The low‐P and high‐T metamorphism continued for c. 100 Ma, which is longer than the active period of a single granitoid body. These findings indicate that an elevation of geotherm and a transition from high‐P and low‐T to low‐P and high‐T metamorphism occurred, associated with continuous emplacement of several granitoids, during the crustal evolution in the Devonian CAOB. 相似文献
20.
Yong–Joo JWA 《Resource Geology》1998,48(4):273-284
Abstract: Five groups of the Phanerozoic granitoids in South Korea can be deduced from their temporal and spatial distributions: (1) Jurassic granitoids in the Gyeonggi massif, (2) Permo-Jurassic granitoids in the Ogcheon belt, (3) Permo-Jurassic granitoids in the Yeongnam massif, (4) Cretaceous granitoids in the Ogcheon belt, and (5) Cretaceous granitoids in the Gyeongsang basin. Though the granitoids of each group generally show calc-alkaline and orogenic natures, the petrological, geochemical and genetical features are different with each other. The Permo-Jurassic granitoids in the Ogcheon belt have lower contents of Al2O3, Fe2O3, CaO, P2O5, but higher of FeO, FeOT, MgO, K2O than those in the Yeongnam massif. From higher feature of K2O, Na2O+K2O and K2O/Na2O, the Ogcheon belt seems to have been located at closer continent side relative to the Yeongnam massif during Permo-Jurassic time. From lower values of Fe2O3/FeO and magnetic susceptibility the granitoids of the Ogcheon belt had been solidified under more reducing environment than those of the Yeongnam massif. The Cretaceous granitoids in the Ogcheon belt have lower contents of TiO2, Fe2O3, FeO, FeOT, CaO and P2O5, but higher of MgO, K2O, Na2O+K2O and K2O/Na2O than those in the Gyeongsang basin. This feature indicates that the Ogcheon belt would correspond to the continental environment of magma genesis during Cretaceous time. Higher values of Fe2O3/FeO and magnetic susceptibility in the Cretaceous granitoids in the Gyeongsang basin suggest that the granitoids had been solidified under highly oxidizing environment. From the particular chemical features of K2O, Na2O+K2O and K2O/Na2O, the Permo-Jurassic granitoids in the Ogcheon belt, the Yeongnam massif as well as the Cretaceous ones in the Gyeongsang basin can be categorized to the continental margin type granite. The Jurassic granitoids in the Gyeonggi massif are possibly of collision type, and the Cretaceous granitoids in the Ogcheon belt of post–orogenic, intra–conti–nent type. The Jurassic granitoids in the Gyeonggi massif had been possibly generated by crustal melting during the collision of Gyeonggi massif to the northern Pyeongnam basin block. The Cretaceous granitoids in the Ogcheon belt had been emplaced at the hinterland of the continental margin during post-orogenic stage of the Honam Shear Zone. The Cretaceous granitoids in the Gyeongsang basin are often compared with Japanese Cretaceous?Paleogene granitoids in their geochemical and genetical natures. For the granitoid composition, the granitoids in the Gyeongsang basin are higher in Fe2O3, Fe2O3/FeO, Na2O, K2O, Na2O+K2O and K2O/Na2O, but lower in Al2O3, FeO, MnO, CaO and P2O5 than the Japanese granitoids. The contents of TiO2, FeOT and MgO are similar in both granitoids. This geochemical contrast would imply that the Cretaceous granitoid magmas in the Gyeongsang basin had been originated at closer place to the continent side under more tensional field, and solidified under more oxidizing environment than the coeval Japanese granitoid magmas. 相似文献