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1.
Optimal deflection of NEOs en route of collision with the Earth 总被引:1,自引:0,他引:1
Recently, a method for the n-body analysis of the velocity change required to deflect a hazardous near-Earth object (NEO) was presented by Carusi et al. [Carusi, A., Valsecchi, G.B., D'Abramo, G., Boattini A., 2002. Icarus 159, 417-422]. We extent this method in order to optimize the velocity change vector instead of its along-track magnitude. From an application of both methods to a fictitious NEO we find Carusi's parallel approach to be reasonable for phases of unperturbed two-body motion. But, for orbit phases inhering third-body perturbations, i.e., for planetary close approaches or prior to a collision, the results obtained from the new method show the radial component of deflection impulse to play a major role. We show that a fivefold greater efficiency can be achieved by a deflection impulse being non-parallel to orbital velocity. The new method is applied to two possible 99942 Apophis impact trajectories in order to provide constraints for future Apophis deflection mission analysis. 相似文献
2.
Summary ?In the south-eastern Altenbergkar–Silbereck area in the eastern Tauern window (Lungau, Salzburg) structurally controlled
precious-metal (Au–Ag) mineralization is hosted in marbles of the Permo(?)-Mesozoic Silbereck Formation and in the underlying
Variscan Central gneiss. During the Alpine otogeny both lithologies were affected by ductile deformation (shearing, D1; folding,
D2/D3) and subsequent brittle deformation (tension gashes, D4; normal faulting, D5) related to the uplift and exhumation of
the Tauern window. Mineralization is controlled by brittle D4 structures. NE–SW trending steeply dipping tension gashes of
the “Tauerngoldgang” type occur within the Central gneiss. Three different marble-hosted ore types following fracture systems
as well as foliation and bedding planes can be distinguished: 1) metasomatic replacement ores, 2) ores in tension gashes and
3) ores in talc-bearing structures, often containing high-grade gold and silver mineralization (native gold in association
with Ag–Pb–Bi–sulfosalts). Four stages of mineralization can be distinguished which occur in all ore types: arsenopyrite–pyrite–pyrrhotite
(first stage), Au–(Ag–Pb–Bi–sulfosalts) (second stage), base-metal sulfides and tetrahedrite–tennantite (third stage) and
Ag-rich galena (fourth stage). Preliminary fluid inclusion data indicate temperatures of ore formation well above 300 °C (346 °C
mean) for the second stage within the Central gneiss and temperatures between 310 and 230 °C for the second and third stages
in the marble.
Received October 12, 2001; revised version accepted September 5, 2002
Published online March 10, 2003 相似文献
3.
4.
奥地利安东帕有限公司 《岩矿测试》2008,27(5):402
Ni、V、Al、Si是石油的天然组分。其中Ni和V来源于形成石油的原始物质,它们易形成大而复杂的分子,从而使沸点非常高。含Ni和V的化合物在提炼过程中无法蒸馏,不能很经济地从燃料中去除。Ni、V、Al、Si在燃烧时会生成不同的氧化物,沉积在化学反应器(如发动机)的冷却器表面,形成黏着物并引起腐蚀;另外这些元素可能灭活提炼过程中的催化剂。可见,测定Ni、V、Al、Si对于炼油工业非常重要。1仪器样品消解采用奥地利安东帕公司(Anton Paar GmbH)生产的Multiwave 3000微波消解系统,配有8位超高压转子。消解后的样品中痕量元素的分析用Optima 3000电感耦合等离子体发射光 相似文献
5.
二氧化锆和三氧化二铝的微波消解 总被引:1,自引:0,他引:1
奥地利安东帕有限公司上海代表处 《岩矿测试》2008,27(6):482
A l2O3和ZrO2具有很高的热稳定性和化学稳定性,可用于高温绝缘,制作挡热板或保护涂层。在纤维状态时,A l2O3和ZrO2可被用作过滤材料或催化剂的载体。通常对A l2O3和ZrO2的纯度要求很高,其中材料的杂质元素如K或Na的含量对最终产品的性能有非常重大的影响。在分析A l2O3和ZrO2中的痕量元素时,最困难的一步是样品的消解,这类氧化物属于最难溶解的材料。传统的熔融分解方法会将杂质带入样品中,湿法消解则是一个理想的选择。湿法消解方法是否可行,取决于样品的晶体结构、杂质元素的含量和样品颗粒的大小。利用适当的酸体系和高性能的微波消解系统,可以在较短的时间内获得理想的分解效果。对于大多 相似文献
6.
Geobarometry for Peridotites: Experiments in Simple and Natural Systems from 6 to 10 GPa 总被引:3,自引:0,他引:3
Experiments with peridotite minerals in simple (MgO–Al2O3–SiO2,CaO–MgO–SiO2 and CaO–MgO–Al2O3–SiO2)and natural systems were conducted at 1300–1500°Cand 6–10 GPa using a multi-anvil apparatus. The experimentsin simple systems demonstrated consistency with previous lowerpressure experiments in belt and piston–cylinder set-ups.The analysis of spatial variations in pyroxene compositionswithin experimental samples was used to demonstrate that pressureand temperature variations within the samples were less than0·4 GPa and 50°C. Olivine capsules were used in natural-systemexperiments with two mineral mixtures: SC1 (olivine + high-Alorthopyroxene + high-Al clinopyroxene + spinel) and J4 (olivine+ low-Al orthopyroxene + low-Al clinopyroxene + garnet). Theexperiments produced olivine + orthopyroxene + garnet ±clinopyroxene assemblages, occasionally with magnesite and carbonate-richmelt. Equilibrium compositions were derived by the analysisof grain rims and evaluation of mineral zoning. They were comparedwith our previous experiments with the same starting mixturesat 2·8–6·0 GPa and the results from simplesystems. The compositions of minerals from experiments withnatural mixtures show smooth pressure and temperature dependencesup to a pressure of 8 GPa. The experiments at 9 and 10 GPa producedandradite-rich garnets and pyroxene compositions deviating fromthe trends defined by the lower pressure experiments (e.g. higherAl in orthopyroxene and Ca in clinopyroxene). This discrepancyis attributed to a higher degree of oxidation in the high-pressureexperiments and an orthopyroxene–high-P clinopyroxenephase transition at 9 GPa. Based on new and previous resultsin simple and natural systems, a new version of the Al-in-orthopyroxenebarometer is presented. The new barometer adequately reproducesexperimental pressures up to 8 GPa. KEY WORDS: garnet; mineral equilibrium; multi-anvil apparatus; orthopyroxene; geobarometry 相似文献
7.
Gerhard Ludwig 《Mineralium Deposita》1966,1(3):193-200
Zusammenfassung Mikroskopische Anschliffe feinkörniger Aufbereitungsprodukte können nur dann quantitativ ausgewertet werden, wenn ihre Schliffqualität so hoch ist, daß auch feinste Partien sicher zu bestimmen sind. Daneben muß gewährleistet sein, daß die an der Schliffoberfläche erfaßten Körner die tatsächliche Verteilung der Mineralien der Probe repräsentieren. Diese Forderung kann nur durch zweckentsprechende Präparation, die dem eigentlichen Schleif- und Polierprozeß vorausgeht, erfüllt werden. Als günstigste Lösung erscheint es, das Korngemisch exakt als Einkornschicht zu präparieren und anschließend wie Stückproben anzuschleifen. Die Schliffe können dann nach den gleichen statistischen Gesetzmäßigkeiten ausgewertet werden, wie sie bei praktisch zweidimensionalen Dünnschliffen oder bei Streupräparaten nichtopaker Korngemische vorliegen.
Mitteilung Nr. 141 aus dem Forschungsinstitut für Aufbereitung der Deutschen Akademie der Wissenschaften zu Berlin, Freiberg (Sachsen). Direktor: Prof. Dr.-Ing. habil. H. Kirchberg. 相似文献
Quantitative examination of fine-grained ore dressing products depends on good quality of the sections and on whether very small particles and areas of grains can be determined. Besides, it must absolutely be guaranteed that the grains at the section surface represent the actual distribution of the minerals in the sample. This condition can only be realized by suitable grain mounting prior to grinding and polishing. The best method for this purpose appears to be the preparation of a mono-grain layer. The polished sections can then be examined according to the same statistical laws as two-dimensional thin sections or immersion-liquid slides of non-opaque mixtures of grains.
Mitteilung Nr. 141 aus dem Forschungsinstitut für Aufbereitung der Deutschen Akademie der Wissenschaften zu Berlin, Freiberg (Sachsen). Direktor: Prof. Dr.-Ing. habil. H. Kirchberg. 相似文献
8.
Stable carbon isotope ratios of plankton carbon and sinking organic matter from the Atlantic sector of the Southern Ocean 总被引:3,自引:0,他引:3
Gerhard Fischer 《Marine Chemistry》1991,35(1-4)
The stable carbon isotope composition of particulate organic carbon (POC) from plankton, sediment trap material and surface sediments from the Atlantic sector of the Southern Ocean were determined. Despite low and constant water temperatures, large variations in the δ13C values of plankton were measured. 13C enrichments of up to 10‰ coincided with a change in the diatom assemblage and a two-fold increase in primary production. Increased CO2 consumption as a result of rapid carbon fixation may result in diffusion limitation reducing the magnitude of the isotope fractionation. The δ13C values of plankton from sea-ice cores display a relationship with the chlorophyll a content. High ‘ice-algae’ biomass, in combination with a limited exchange with the surrounding seawater, results in values of about − 18 to − 20‰. It is assumed that these values are related to a reduced CO2 availability in the sea-ice system. In comparison with plankton, sinking krill faeces sampled by traps can be enriched by 2–5‰ in 13C (e.g. central Bransfield Strait). In contrast, the transport of particles in other faeces, diatom aggregates or chains results in minor isotope changes (e.g. Drake Passage, Powell Basin, NW Weddell Sea). A comparison between the δ13C values of sinking matter and those of surface sediments reveals that 13C enrichments of up to 3–4‰ may occur at the sediment-water boundary layer. These isotopic changes are attributed to high benthic respiration rates. 相似文献
9.
Microbial Biomass Dynamics Along a Trophic Gradient at the Atlantic Barrier Reef off Belize (Central America) 总被引:2,自引:0,他引:2
Abstract. Recent findings indicate that heterotrophic bacteria and not phytoplankton are the most numerous biomass components even in the euphotic zone of oligotrophic, open oceans. In this study it was hypothesized that the microbial biomass components change within a few hundred meters as oligotrophic water flows across the reef and becomes enriched with nutrients. Along a trophic gradient, four stations at the Atlantic Barrier Reef off Belize (Central America) were sampled for microbial biomass components. Phytoplankton biomass (measured as chlorophyll a) ranged from the most oligotrophic station (St. 1) to the most eutrophic station (St. 4) from 6.9–415.5 μg CI"' (assuming a C:chl a ratio of 30): heterotrophic bacterial biomass increased 4-fold (from 10.1–46.4μg C 1-1 ), heterotrophic nanoflagellate (HNAN) biomass increased from 4.6-19ug C 1-1 , and cyanobacteria from 0.9-4.5 μg C-1-1 . Production estimates derived from seawater cultures revealed a 5-fold increase in bacterial production from the oligotrophic station (3.7 ug C 1-1 d-1 ) to the eutrophic St. 4 (17.8ug C-1-d1-1 )- Cyanobacterial production rose from 1.1–3.5ug C-1–d-1 and HNAN production from 0.65-1.13 μg C-1-1 -d-1 . While cyanobacteria contributed between 13 and 20% to the autotrophic plankton component in the oligotrophic waters, their contribution dropped to about 1 % at the eutrophic stations. 相似文献
10.