三维地震小面元采集技术在晋城矿区的应用

依托“西部煤炭资源高精度三维地震勘探技术”工程,对晋城矿区进行了旨在提高小断层,小陷落柱探测能力的高密度三维地震勘探。根据面元选择因素及该区地质任务,采用5m×5m网格进行野外数据采集;考虑炮检距、方位角、覆盖次数、排列片横纵比及煤层埋深（350～500m）等因素,采用中点放炮、60道接收,24次覆盖（横向4次,纵向6次）的8线16炮束状观测系统,基岩中激发。原始资料经同一处理流程后,获得5m×5m×1ms、5m×10m×1ms、10m×10m×1ms及2.5m×2.5m×1ms不同单元的三维数据体多个,通过对比可以发现小断层,小陷落柱在其小面元叠加时间剖面、顺层切片及相干切片都有清晰的反映。实例说明,小面元采集技术可以提高对小构造的纵、横向分辨能力,满足山区对三维地震精确勘探的要求。     

小面元三维地震勘探技术在西山屯兰矿南五采区的应用

屯兰矿南五采区地形复杂,最大高差达271m,地表大面积为第四系黄土覆盖,激发困难。为探索研究小面元三维地震勘探技术的应用效果。在常规三维地震勘区域内划出1km^2,采用5m×5m小面元进行采集。在地震数据采集过程中,采取了加大激发井深、提高覆盖次数、减小CMP面元网格和加大接收排列等技术措施,做到“四小三高、二中一深、两个等高面”。通过插值、抽线及扩大面元处理。获得2．5m×2．5m×1ms、5m×5m×1ms、5m×10m×1ms、10m×10m×1ms以及不同叠加次数的三维数据体。资料解释工作主要是在5m×5m×1ms、2．5m×2．5m×1ms两个数据体上进行,解释落差大于或等于5m的断层6条,落差3～5m的断层8条;查明长轴直径20～30m的陷落柱4个。30～100m的陷落柱1个,大于100m的陷落柱3个。与相邻区常规三维地震比较,小面元三维地震勘探有利于对小陷落柱、小断层的控制和解释。     

三维地震技术在煤层顶板稳定性研究中的应用

龙固井田为全隐蔽的华北型煤田,位于巨野煤田中部,其首采扩大区主采煤层为3号煤层。考虑3煤层顶板稳定性主要受其顶板的构造信息和岩性信息影响,因此首先依据三维地震勘探综合解释成果及波阻抗反演解释成果对二者进行定量化,然后对波阻抗数据进行归一化处理,使得波阻抗数据和量化后的构造数据具有相同的变化范围及等量贡献。在此距离范围内构造和岩性的权值各为0．5,依此生成综合因素煤层顶板稳定性隶属度。分析3煤层顶板以上10m、20m处的综合因素煤层顶板稳定性隶属度图可以发现,该区3煤层顶板稳定性比较好。且其稳定性主要是受构造因素控制,岩性因素相对影响较小。     

基于GIS组件与ANN耦合技术的矿井构造复杂程度评价

矿井构造是影响煤矿安全生产的主要因素,对瓦斯突出、矿井突水有着明显的控制作用。矿井构造具有空间性和非线性等特点,使矿井构造复杂程度评价的难度较大,据此利用MapObjects的空间分析功能和非线性人工神经网络（ANN）耦合技术,对矿井构造复杂程度进行评价。根据前人的研究成果,将突水系数、底板倾角变异系数、底板标高变异系数、断层强度指数、断层密度等5项指标引入评价体系,经过空间分析统计和模型识别,建立了矿井构造复杂程度评价模型。在开滦矿区东欢矿8煤层构造复杂程度的评价中,共训练及评价了研究区的226个评价单元．评价结果表明研究区西部及西北部构造复杂,中部及东南部构造相对简单。     

New basis for the constitutive modelling of aggregated soils

Natural and compacted soils are usually characterized by aggregation of particles. The mechanical behaviour of these materials depends on soil structure. The oedometric compression tests performed on aggregated samples presented here showed that these materials exhibit a yield limit depending not only on stress history and stress state but also on soil structure. Evidence is provided using the neutron tomography technique. These results revealed that soil structure modification occurs together with plastic deformations. The experimental results are used to propose a new state parameter to quantify the soil structure. Based on pore-scale experimental observations, an evolution law for this parameter is proposed as a function of associated plastic strains. Considering both soil fabric and inter-particle bonding effects, a new yield limit depending on stress state, stress history and soil structure is introduced for the aggregated soils. Accordingly, a new constitutive framework consistent with strain hardening plasticity is proposed to consider soil structure effects in the modelling of aggregated soils.     

Changing grading of soil: effect on critical states

Examples of situations are presented where the grading of a soil changes during its lifetime either by crushing of particles leading to an increase of fine material or by slow transport of fine particles with seepage leading to a decrease of fine material. Such grading changes influence the basic constitutive properties of the soil, in particular properties such as critical states which are dependent on the available range of densities of packing. Discrete element modelling is used to show the dependence of critical state conditions on grading and the way in which the particle assembly seeks out new critical state conditions as the grading changes.     

Rate constants for the reactions of the NO3 radical with HCOOH/HCOO− and CH3COOH/CH3COO− in aqueous solution between 278 and 328 K

The kinetics of the aqueous phase reactions of NO₃ radicals with HCOOH/HCOO^– and CH₃COOH/CH₃COO^– have been investigated using a laser photolysis/long-path laser absorption technique. NO₃ was produced via excimer laser photolysis of peroxodisulfate anions (S₂O ₈ ^2– ) at 351 nm followed by the reactions of sulfate radicals (SO ₄ ^– ) with excess nitrate. The time-resolved detection of NO₃ was achieved by long-path laser absorption at 632.8 nm. For the reactions of NO₃ with formic acid (1) and formate (2) rate coefficients ofk ₁=(3.3±1.0)×10⁵ l mol^–1 s^–1 andk ₂=(5.0±0.4)×10⁷ l mol^–1 s^–1 were found atT=298 K andI=0.19 mol/l. The following Arrhenius expressions were derived:k ₁(T)=(3.4±0.3)×10¹⁰ exp[–(3400±600)/T] l mol^–1 s^–1 andk ₂(T)=(8.2±0.8)×10¹⁰ exp[–(2200±700)/T] l mol^–1 s^–1. The rate coefficients for the reactions of NO₃ with acetic acid (3) and acetate (4) atT=298 K andI=0.19 mol/l were determined as:k ₃=(1.3±0.3)×10⁴ l mol^–1 s^–1 andk ₄=(2.3±0.4)×10⁶ l mol^–1 s^–1. The temperature dependences for these reactions are described by:k ₃(T)=(4.9±0.5)×10⁹ exp[–(3800±700)/T] l mol^–1 s^–1 andk ₄(T)=(1.0±0.2)×10¹² exp[–(3800±1200)/T] l mol^–1 s^–1. The differences in reactivity of the anions HCOO^– and CH₃COO^– compared to their corresponding acids HCOOH and CH₃COOH are explained by the higher reactivity of NO₃ in charge transfer processes compared to H atom abstraction. From a comparison of NO₃ reactions with various droplets constituents it is concluded that the reaction of NO₃ with HCOO^– may present a dominant loss reaction of NO₃ in atmospheric droplets.     

Modelling of the vertical fluxes of nitric acid,ammonia, and ammonium nitrate

Results from numerical investigations regarding the exchange of HNO₃, NH₃, and NH₄NO₃ between the atmosphere and the biosphere are presented. The investigations were performed with a modified inferential method which is based on the generally accepted micrometeorological ideas of the transfer of momentum, sensible heat and matter near the Earth's surface and the chemical reactions among these nitrogen compounds. This modified inferential method calculates the micrometeorological quantities (such as the friction velocity and the fluxes of sensible and latent heat), the height-invariant fluxes of the composed chemically conservative trace species with group concentrationsc ₁=[HNO₃]+[NH₄NO₃] (total nitrate),c ₂=[NH₃]+[NH₄NO₃] (total ammonia), andc ₃=[HNO₃]-[NH₃] as well as the fluxes of the individual nitrogen compounds. The parameterization of the fluxes is based on the flux-gradient relationships in the turbulent region of the atmospheric surface layer. The modified inferential method requires only the data of wind velocity, temperature, humidity and concentrations (HNO₃, NH₃, and NH₄NO₃) measured at a reference height by stations of a monitoring network.     

LonGSp: A near infra-red spectrometer

We present a new cooled grating near infra-red spectrometer designed to acquire spectra at the TIRGO telescope in the 0.9÷2.5m region with a resolving power of 300÷4000, equipped with a Rockwell NICMOS 3 detector.     

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

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.