塔河油田2区三叠系油藏类型初步探讨     

康立功 《安徽地质》2008,18(1):20-26

塔河油田2区三叠系油藏是西北分公司开发较早的碎屑岩油藏之一,开发层系有上油组、中油组,油柱高度在15～20m,储层为辫状三角洲相辫状三角洲前缘亚相水下分流河道、河口坝、分流间湾微相沉积,非均质性严重。本区上油组砂体厚度40～0m,中油组25～35m,分布较稳定,物性为中孔、中高渗储层,原油属低粘度轻质油。但2区三叠系油藏实钻变化大,见水快、产量递减快、含水上升快、采出程度低,开发效果较差,经过多次调整虽有一定程度改善,仍存在一些问题。本文认为2区三叠系油藏开发效果较差的原因之一是对本区油藏类型的认识上存在问题即2区三叠系油藏是以断裂控制的断块油藏而非背斜油藏,并延伸分析正在投入开发评价的S96-T901井区、TK232-T453井区及T206-T208井区等都为断块（断背斜）油藏。应用断块油藏的观点对塔河地区三叠系油藏勘探开发有重要指导意义。  相似文献   

甘肃大泉水——白沙岘矿区含煤地层及煤层赋存特征     

李玉畅 《中国煤炭地质》2008,(11):9-11

大泉水-白沙岘矿区位于甘肃省景泰县境内,在大地构造位置上处于北祁连加里东褶皱带东段,区内含煤地层为下石炭统靖远组和上石炭统羊虎沟组,属海陆交互相含煤沉积,根据岩性、岩相特征可划分为两个沉积旋回。该矿区主要可采煤层煤．层组赋存于羊虎沟组,厚1．71～9．00m,沿走向由西向东厚度变小,在大泉水井田可采厚度主要分布在V线以西,其东区段只是零星分布且不可采;在白沙岘井田煤层总厚度为2．99～5．15m,厚度变化小,属稳定煤层。煤：层组赋存于靖远组,仅分布在大泉水井田,厚1．33～8．88m,沿走向由西向东呈长透镜体状,西段和中段煤层发育较好．V线以东区段煤层变薄并出现无煤区。  相似文献   

我国煤炭航测技术的最新发展     

赖百炼 《中国煤炭地质》2008,(11):81-83

中国煤炭地质总局航测遥感局作为我国煤炭航测技术的主要单位,承担着95％以上的煤炭矿区航测成图任务,并逐步发展成为我国集航空摄影、遥感地质、地图制印、地下管线探测、地理信息技术等全面发展的空间信息产业集团：伴随着计算机技术的发展,煤炭航测技术走过了从模拟测图到解析测图,最后发展到今天的全数字测图的历程。目前煤航已拥有和掌握了IMU／DGPS辅助航空摄影技术、SAR（合成孔径雷达）成图技术、LIDAR（机载激光扫描）技术等空间数据采集最新技术。  相似文献   

Actinic flux and photolysis frequency comparison computations using the model PHOTOGT     

Carsten Blindauer  Vladimir Rozanov  John Philip Burrows 《Journal of Atmospheric Chemistry》1996,24(1):1-21

The accurate radiative transfer model GOMETRAN, initially designed to yield radiances at TOA in the wavelength range 240–790 nm, has been extended to allow for the computation of actinic fluxes down to 175 nm and for the calculation of photolysis frequencies in the atmosphere. The capability of the extended model PHOTOGT (PHOTOGOMETRAN) is demonstrated in a number of successful comparison studies both with recent experiments (ground-based, balloonborne, airborne) and model calculations of radiances, actinic fluxes and photolysis frequencies in the stratosphere and troposphere. In an atmospheric case study, the impact of new quantum yield data for the O₃ » O₂+O(¹ d) photodissociation channel on the photolytic production of O(¹ d) atoms in the lower atmosphere has been quantified.  相似文献   

    

Daniel Y. Gezari  Dana E. Backman 《Astrophysics and Space Science》1995,224(1-2):463

Mid-infrared imaging photometry of the Orion BN/KL infrared cluster at eight wavelengths between 5 and 20µm using a 58 × 62 pixel imaging array camera has revealed new compact sources and the large-scale structure of the region in diffraction-limited (1 arcsec) detail. Several new objects have been detected within a few arcsec of IRc2, widely thought to be the principal luminosity source for the entire BN/KL complex. Detailed color temperature and emission opacity images are derived from the 7.8, 12.4 and 20.0µm observations, and the 9.8µm image is used to derive an image of silicate dust extinction for the region. The color temperature, opacity, and extinction images show that IRc2 may not be the single dominant luminosity source for the BN/KL region; substantial contributions to the luminosity could be made by IRc7, BN, KL, and five new compact 10µm sources detected within a few arcseconds of IRc2. We suggest that a luminous, early-type star near IRc2, which is associated with the compact radio source I and the Orion SiO maser, is the dominant luminosity source in the BN/KL region, hidden from view by cool dust material with at least Av 60 mag of visible extinction.  相似文献   

Seasonal variations of atmospheric sulfur dioxide and dimethylsulfide concentrations at Amsterdam Island in the southern Indian Ocean     

J. P. Putaud  N. Mihalopoulos  B. C. Nguyen  J. M. Campin  S. Belviso 《Journal of Atmospheric Chemistry》1992,15(2):117-131

Daily measurements of atmospheric sulfur dioxide (SO₂) concentrations were performed from March 1989 to January 1991 at Amsterdam Island (37°50 S–77°30 E), a remote site located in the southern Indian Ocean. Long-range transport of continental air masses was studied using Radon (²²²Rn) as continental tracer. Average monthly SO₂ concentrations range from less than 0.2 to 3.9 nmol m^-3 (annual average = 0.7 nmol m^-3) and present a seasonal cycle with a minimum in winter and a maximum in summer, similar to that described for atmospheric DMS concentrations measured during the same period. Clear diel correlation between atmospheric DMS and SO₂ concentrations is also observed during summer. A photochemical box model using measured atmospheric DMS concentrations as input data reproduces the seasonal variations in the measured atmospheric SO₂ concentrations within ±30%. Comparing between computed and measured SO₂ concentrations allowed us to estimate a yield of SO₂ from DMS oxidation of about 70%.  相似文献   

Latitudinal variation of measured O3 photolysis frequencies J(O1D) and primary OH production rates over the Atlantic Ocean between 50° N and 30° S     

A. Hofzumahaus  T. Brauers  U. Platt  J. Callies 《Journal of Atmospheric Chemistry》1992,15(3-4):283-298

The latitudinal variation of the photolysis frequency of ozone to O(¹D) atoms, J(O¹D), was measured using a filter radiometer during the cruise ANT VII/1 of the research vessel Polarstern in September/October 1988. The J(O¹D) noon values exhibited a maximum of 3.6×10^-5 s^-1 (2 sr) at the equator and decreased strongly towards higher latitudes. J(O¹D) reached highest values for clean marine background air with low aerosol load and almost cloudless sky. The J(O¹D) data, measured under these conditions and a temperature of 295 K, can be expressed by: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamOsaiaacI% cacaqGpbWaaWbaaSqabeaaiiaacqWF8baFaaGccaqGebGaaeykaiaa% bccacqWF9aqpcaqGGaGaaeyzaiaabIhacaqGWbGaaeiiaiaabUhacq% GHsislcaaI4aGaaiOlaiaaicdacaaIYaGaeyOeI0IaaGioaiaac6ca% caaI4aGaaiiEaiaaigdacaaIWaWaaWbaaSqabeaacqGHsislcaaIZa% aaaOGaaeiiaiaabIhacaqGGaGaam4uaiabgUcaRiaaiodacaGGUaGa% aGinaiaacIhacaaIXaGaaGimamaaCaaaleqabaGaeyOeI0IaaGOnaa% aakiaadofadaahaaWcbeqaaiaaikdaaaGccaGG9bGaaeikaiaaboha% daahaaWcbeqaaiabgkHiTiaaigdaaaGccaGGPaaaaa!5EE9!\[J({\text{O}}^| {\text{D) }} = {\text{ exp \{ }} - 8.02 - 8.8x10^{ - 3} {\text{ x }}S + 3.4x10^{ - 6} S^2 \} {\text{(s}}^{ - 1} )\] where S represents the product of the overhead ozone column (DU) and the secant of the solar zenith angle. The meridional profile of the primary OH radical production rate P(OH) was calculated from the J(O¹D) measurements and simultaneously recorded O₃ and H₂O mixing ratios. While the latitudinal distribution of J(O¹D) and water vapour was nearly symmetric to the equator, high tropospheric ozone levels up to 40 ppb were observed in the Southern Hemisphere, SH, resulting in higher P(OH) in the SH.  相似文献   

Trace gas exchange at the air/water interface: Measurements of mass accommodation coefficients     

W. Kirchner  F. Welter  A. Bongartz  J. Kames  S. Schweighoefer  U. Schurath 《Journal of Atmospheric Chemistry》1990,10(4):427-449

A liquid jet of 90 m diameter and variable length has been utilized to determine absorption rates and, hence, mass accommodation coefficients , of atmospheric trace gases. The compounds investigated are HCl (0.01), HNO₃ (0.01), N₂O₅ (0.005), peroxyacetyl nitrate (>0.001), and HONO (0.005). It is concluded that the absorption of these trace gases by liquid atmospheric water is not significantly retarded by interfacial mass transport. The strengths and limitations of the liquid jet technique for measuring mass accommodation coefficients are explored.  相似文献   

Fluid sources for the La Guitarra epithermal deposit (Temascaltepec district, Mexico): Volatile and helium isotope analyses in fluid inclusions   总被引：1，自引：0，他引：1  

Antoni Camprubí  Beverly A. Chomiak  Ruth E. Villanueva-Estrada  David I. Norman  Martin Stute 《Chemical Geology》2006,231(3):252-284

The La Guitarra deposit (Temascaltepec district, South-Central Mexico), belongs to the low/intermediate sulfidation epithermal type, has a polymetallic character although it is currently being mined for Ag and Au. The mineralization shows a polyphasic character and formed through several stages and sub-stages (named I, IIA, IIB, IIC, IID, and III). The previous structural, mineralogical, fluid inclusion and stable isotope studies were used to constrain the selection of samples for volatile and helium isotope analyses portrayed in this study. The N₂/Ar overall range obtained from analytical runs on fluid inclusion volatiles, by means of Quadrupole Mass Spectrometry (QMS), is 0 to 2526, and it ranges 0 to 2526 for stage I, 0 to 1264 for stage IIA, 0 to 1369 for stage IIB, 11 to 2401 for stage IIC, 19 to 324 for stage IID, and 0 to 2526 for stage III. These values, combined with the CO₂/CH₄ ratios, and N₂-He-Ar and N₂-CH₄-Ar relationships, suggest the occurrence of fluids from magmatic, crustal, and shallow meteoric sources in the forming epithermal vein deposit. The helium isotope analyses, obtained by means of Noble Gas Mass Spectrometry, display R/Ra average values between 0.5 and 2, pointing to the occurrence of mantle-derived helium that was relatively diluted or “contaminated” by crustal helium. These volatile analyses, when correlated with the stable isotope data from previous works and He isotope data, show the same distribution of data concerning sources for mineralizing fluids, especially those corresponding to magmatic and crustal sources. Thus, the overall geochemical data from mineralizing fluids are revealed as intrinsically consistent when compared to each other.The three main sources for mineralizing fluids (magmatic, and both deep and shallow meteoric fluids) are accountable at any scale, from stages of mineralization down to specific mineral associations. The volatile and helium isotope data obtained in this paper suggest that the precious metal-bearing mineral associations formed after hydrothermal pulses of predominantly oxidized magmatic fluids, and thus it is likely that precious metals were carried by fluids with such origin. Minerals from base-metal sulfide associations record both crustal and magmatic sources for mineralizing fluids, thus suggesting that base metals could be derived from deep leaching of crustal rocks. At the La Guitarra epithermal deposit there is no evidence for an evolution of mineralizing fluids towards any dominant source. Rather than that, volatile analyses in fluid inclusions suggest that this deposit formed as a pulsing hydrothermal system where each pulse or set of pulses accounts for different compositions of mineralizing fluids.The positive correlation between the relative content of magmatic fluids (high N₂/Ar ratios) and H₂S suggests that the necessary sulfur to carry mostly gold as bisulfide complexes came essentially from magmatic sources. Chlorine necessary to carry silver and base metals was found to be abundant in inclusion fluids and although there is no evidence about its source, it is plausible that it may come from magmatic sources as well.  相似文献   

Hydrometallurgical processing and recovery of molybdenum trioxide from spent catalyst   总被引：5，自引：0，他引：5  

Kyung Ho Park  B. Ramachandra Reddy  D. Mohapatra  Chul-Woo Nam 《International Journal of Mineral Processing》2006,80(2-4):261-265

Hydrometallurgical processing of spent hydrodesulphurisation (HDS) catalyst for the recovery of molybdenum using sodium carbonate and hydrogen peroxide mixtures was investigated. The results indicated that the recovery of molybdenum was largely dependent on the concentrations of Na₂CO₃ and H₂O₂ in the reaction medium, which controls the acidity of the leach liquor and carry over of impurities such as Al, Ni, P, Si and V. Leaching process was exothermic and leaching efficiency of molybdenum decreased with increasing solid to liquid ratio. Large scale leaching of spent catalyst, under optimum conditions: 20% pulp density, 85 g/L Na₂CO₃, 10 vol.% H₂O₂ and 1 h reaction, resulted a leaching efficiency of 84% Mo. The obtained leach liquor contained (g/L): Mo — 22.0, Ni — 0.015 and Al — 0.82, P — 1.1, Si — 0.094 and minor quantities of V — 8 mg/L, As and Co — < 1 mg/L. Recovery of Mo from leach solution as MoO₃ of 97.30% purity was achieved by ammonium molybdate precipitation method.  相似文献