略论煤的变质问题

我国煤的变质作用根据受热的主要热源及其作用方式和煤质特征，可归纳为三种基本类型。即：深成变质作用、岩浆热变质作用和动力变质作用。此外，1988年中国地质大学潘治贵等，通过对青海热水矿区研究发现而命名为一种新变质作用类型-热水变质作用。在前人研究的基础上，笔者拟就影响变变质的主要因素谈谈看法，供讨论。     

The use of GPS arrays in detecting shock-acoustic waves generated during rocket launchings

This paper is concerned with the parameters of shock-acoustic waves (SAW) generated during rocket launchings. We have developed the interferometric method for determining SAW parameters (including angular characteristics of the wave vector, and the SAW phase velocity, as well as the direction towards the source) using GPS-arrays. Contrary to the conventional radio-probing techniques, the proposed method provides an estimate of SAW parameters without a priori information about the site and time of a rocket launching. The application of the method is illustrated by a case study of ionospheric effects from launchings of rockets PROTON, SOYUZ and SPACE SHUTTLE from Baikonur and Kennedy Space Center cosmodromes in 1998–2000. In spite of a difference of rocket characteristics, the ionospheric response for all launchings had the character of an N-wave corresponding to the form of a shock wave. The SAW period T is 270–360 s, and the amplitude exceeds the standard deviation of total electron content background fluctuations in this range of periods under quiet and moderate geomagnetic conditions by factors of 2–5 as a minimum. The angle of elevation of the SAW wave vector varies from 30° to 60°, and the SAW phase velocity (900–1200 m/s) approaches the sound velocity at heights of the ionospheric F-region maximum. The position of the SAW source, inferred by neglecting refraction corrections, corresponds to the segment of the rockets path at a distance no less than 200–900 km from the launch pad, and to the rocket flying altitude no less than 100 km. Our data are consistent with the existing view that SAW are generated during a nearly horizontal flight of the rocket with its engine in operation in the acceleration segment of the path at 100–130 km altitudes in the lower atmosphere.     

Quantitative description of electron precipitation during auroral absorption events in the morning/noon local-time sector

Flux-energy spectra of precipitating electrons are derived from electron density profiles measured by the EISCAT radar during auroral absorption events in the morning/noon local-time sector. The inversion technique uses effective recombination coefficient profiles computed on the basis of a previously validated theoretical model of the lower ionosphere. It is shown that flux-energy spectra for the energy range 30–200 keV are in reasonable agreement with those derived for the same events using trapped flux-energy spectra from geosynchronous satellite data and a model for diffusion of trapped electrons into the loss cone by scattering on whistler waves. During individual events, strongly varying precipitating fluxes are found to be due primarily to varying pitch-angle diffusion.     

Location and quantitative analysis of OH in coesite

 The incorporation of hydrogen (deuterium) into the coesite structure was investigated at pressures from 3.1 to 7.5 GPa and temperatures of 700, 800, and 1100 °C. Hydrogen could only be incorporated into the coesite structure at pressures greater 5.0 GPa and 1100 °C . No correlation between the concentration of trace elements such as Al and B and the hydrogen content was observed based on ion probe analysis (1335 ± 16 H ppm and 17 ± 1 Al ppm at 7.5 GPa, 1100 °C). The FTIR spectra show three relatively intense bands at 3575, 3516, and 3459 cm⁻¹ (ν₁ to ν₃, respectively) and two very weak bands at 3296 and 3210 cm⁻¹ (ν₄ and ν₅, respectively). The band at 3516 cm⁻¹ is strongly asymmetric and can be resolved into two bands, 3528 (ν_2a) and 3508 (ν_2b) cm⁻¹, with nearly identical areas. Polarized infrared absorption spectra of coesite single-crystal slabs, cut parallel to (0 1 0) and (1 0 0), were collected to locate the OH dipoles in the structure and to calibrate the IR spectroscopy for quantitative analysis of OH in coesite (ɛ _{i ,tot}=190 000 ± 30 000 l mol⁻¹ _H2O cm⁻²). The polarized spectra revealed a strong pleochroism of the OH bands. High-pressure FTIR spectra at pressures up to 8 GPa were performed in a diamond-anvil cell to gain further insight into incorporation mechanism of OH in coesite. The peak positions of the ν₁, ν₂, and ν₃ bands decrease linearly with pressure. The mode Grüneisen parameters for ν₁, ν₂, and ν₃ are −0.074, −0.144 and −0.398, respectively. There is a linear increase of the pressure derivatives with band position which follows the trend proposed by Hofmeister et al. (1999). The full widths at half maximum (FWHM) of the ν₁, ν₂, and ν₃ bands increase from 35, 21, and 28 cm⁻¹ in the spectra at ambient conditions to 71, 68, and 105 in the 8 GPa spectra, respectively. On the basis of these results, a model for the incorporation of hydrogen in coesite was developed: the OH defects are introduced into the structure by the substitution Si^4+(Si2)+4O²⁻= ^[4]□^(Si2) + 4OH⁻, which gives rise to four vibrations, ν₁, ν_2a, ν_2b, and ν₃. Because the OH(D)-bearing samples do contain traces of Al and B, the bands ν₄ and ν₅ may be coupled to Al and/or B substitution. Received: 19 December 2000 / Accepted: 23 April 2001     

低地球轨道（LEO）的大型航天器充电

本文根据ＬＥＯ中等离子体温度低，密度高，德拜长度小的特点，采用薄鞘层近似，计算了离子收集电流；根据电流平衡方程，考虑表面二次电子发射，计算了大型航天器表面在沉降电子流辐照下的充电特性。     

秦皇岛市断裂断层泥的SEM特征与断裂活动性

在野外地质调查的基础上，通过研究秦皇岛市Ｆ１、Ｆ２、Ｆ３断裂断层泥中石英颗粒表面的ＳＥＭ特征，认为Ｆ１断裂最末一次活动时间在早更新世至中更新世；Ｆ２断裂最末一次活动时间在晚更新世中晚期；Ｆ３断裂最末一次活动时间在晚更新世末或全新世初。     

肇东陨石低钙辉石超微结构的研究

在肇东陨石低钙辉石中观察到各种堆垛缺陷,包括斜方-单斜辉石相转变、畴结构、2.7nm长周期结构以及自然界极为罕见的奇数倍八面体层堆垛缺陷——1.35nm等。高分辨像所揭示的1.35nm的新特征是可以重复两次。文中提出1.35nm的结构是“A+B+A-”型。1.35nm片晶仅见于3,4型球粒陨石,因而它可作为由原顽火辉石淬冷形成的、末遭受后期热变质的典型结构。奇数倍0.9nm宽度单斜辉石片晶在吉林陨石(H5)、安龙陨石(H5)及东台陨石(LL6)中均有出现,它表明这些陨石的辉石都曾由原顽火辉石转变而成。 肇东陨石低钙辉石中相当频繁的相变以及高能量的奇数倍0.45nm层堆垛缺陷的存在,可能表明该陨石形成于退变质过程。     

Lower palaeozoic and precambrian petroleum source rocks and the coalification path of alginite

Organic-rich samples derived from a Middle Cambrian Formation in the Georgina Basin, and from the Middle Proterozoic of the McArthur Basin in northern and central Australia, yielded alginite ranging from immature oil shale material to overmature residue. A maturation scale has been developed based on the thermal evolution of alginite as determined from reflectance and fluorescence. The coalification path of alginite is marked by jumps in contrast to the linear path of wood-derived vitrinite. Six zones have been recognised, ranging from undermature (zone I), through the mature (zones II/III), followed by a stable stage of no change (zone IV) to the overmature (zones V and VI). The onset of oil generation in alginite as evident from the present study is at 0.3% R_{o Alg.} and is expressed in a change of fluorescence from yellow to brown, and a coalification jump from 0.3 to 0.6% R_o of Alg. In many boreholes zone III can be distinguished between 0.6 and 0.8% R_o of Alg. where subsequent oil generation occurs. Zones II and III represent the oil window.A zone of little or no change designated zone IV, at of alginite follows zones II/III. A marked coalification jump characterises zone V, where a pronounced change in reflectance occurs to >1.0% R_{o Alg.}, signifying peak gas generation. The border of oil preservation lies at the transition of zone V and VI, at 1.6% R_{o Alg.} In zone VI gas generation only occurs.Comparison of reflectance results with experimental and geochemical pyrolysis data supports high activation energies for hydrocarbon generation from alginite, and therefore a later onset of oil generation than other liptinite macerals (i.e. cutinite, exinite, resinite) as well as a narrow oil window.Transmission electron microscopy (TEM) confirms that alginite does not go through a distinct intermediate stage but that the percentage of unreacted organic matter decreases as maturation proceeds. A clear distinction can be made in TEM between immature alginite, alginite after oil generation, and alginite residue following gas generation. Alginite beyond 1.6% R_o acquires very high densities and the appearance of inertinite in TEM.Bitumens/pyrobitumens make a pronounced contribution to the organic matter throughout the basins and have been shown to effect pyrolysis results by suppressing T_max. The bitumens/pyrobitumens have been divided into four groups, based on their reflectance and morphology, which in turn appears to be an expression of their genetic history. Their significance is in aiding the understanding of the basins' thermal history, and the timing of oil and gas generation.     

Electron Microscopic Study of Manganese Minerals in the Polymetallic Nodules from the Central Pacific Ocean

Manganese minerals in the polymetallic nodules from the Central Pacific Ocean were studied using electron microscopy. The principal Mn minerals, being vernadite and todorokite, exhibit different electron diffraction patterns and morphological features. According to its morphological feature, todorokite shows three phases: fibrous, lamellar and lath-shaped. Both vernadite and todorokite are authigenic minerals. While vernadite was mainly precipitated directly from the relevant solution by microbiological oxidation, todorokite was separated from the solution chemically without the help of microbe. Hence, these two minerals show a close genetic relation.     

拜城县黑英山霞石正长岩矿物学特征研究

霞石正长岩是重要的炼铝资源和陶瓷、玻璃原料。文中利用扫描电镜、X衍射、红外线、电子探针等,综合分析方法对黑英山霞石正长岩的矿物学特征作了详细研究。着重描述了岩石的矿物组合、矿物生成及变化特征。对主要矿物进行了化学成分及X衍射分析,测得霞石成分:SiO_243.66％,Al_2O_330.97％,K_2O4.23％,Na_2O18.46％(Na_2O高于其它地区的霞石)。根据霞石单矿物实测成分计算出其晶体化学分子式为:(K_(0.525)Na_(3.528)Ca_(0.012))_(4.065)[Cr_(0.010)Al-(3.559)Mg_(0.009)Fe_(0.054)Mn_(0.012)Ti_(0.008)Si_(4.258)O_(16)];测得霞石的主要X衍射d值为:0.302～0.303,0.386～0.389,0.1388～0.1391(nm)。测得微斜长石的成分:SiO_264.82％,Al_2O_319.68％,K_2O11.77％,Na_2O2.30％,求得其三斜度△=0.83～1.00,属低微斜长石。通过霞石正长岩中钾长石与霞石矿物中对K原子分配值计算和作图,解得矿物生成温度为400～500℃。测得岩石中的钠长石主要为低钠长石,属后期交代矿物。