氧化亚氮双组元发动机热力性能计算分析

对绿色推进剂N2O,H2,CH3OH,C2H5OH,CH4,C2H6,C2H4,C2H2,C3H8及C3H6的物性进行了全面比较,并采用吉布斯最小自由能法对9种氧化亚氮双组元推进剂组合的热力性能展开全面计算及分析。N2O/H2组合由于其最低的燃气平均摩尔质量而具有最高的比冲;N2O/C2H2组合由于C2H2很高的标准生成焓其燃烧温度可高达3823 K;碳氢燃料在余氧系数α<0.4富燃工况下燃气中含有固碳颗粒,且摩尔含量随着α的降低而急剧升高,喷管出口处可高达35%～40%;N2O/C3H8和N2O/C3H6组合拥有很好的空间应用物性和较高的热力性能,在压比pc:pe=70 atm:1 atm工况下平衡流比冲分别为2 639 m/s和2 656 m/s,具有很好的应用前景。     

Energy, chemical disequilibrium, and geological constraints on Europa

Europa is a prime target for astrobiology. The presence of a global subsurface liquid water ocean and a composition likely to contain a suite of biogenic elements make it a compelling world in the search for a second origin of life. Critical to these factors, however, may be the availability of energy for biological processes on Europa. We have examined the production and availability of oxidants and carbon-containing reductants on Europa to better understand the habitability of the subsurface ocean. Data from the Galileo Near-Infrared Mapping Spectrometer were used to constrain the surface abundance of CO(2) to 0.036% by number relative to water. Laboratory results indicate that radiolytically processed CO(2)-rich ices yield CO and H(2)CO(3); the reductants H(2)CO, CH(3)OH, and CH(4) are at most minor species. We analyzed chemical sources and sinks and concluded that the radiolytically processed surface of Europa could serve to maintain an oxidized ocean even if the surface oxidants (O(2), H(2)O(2), CO(2), SO(2), and SO(4) (2)) are delivered only once every approximately 0.5 Gyr. If delivery periods are comparable to the observed surface age (30-70 Myr), then Europa's ocean could reach O(2) concentrations comparable to those found in terrestrial surface waters, even if approximately 10(9) moles yr(1) of hydrothermally delivered reductants consume most of the oxidant flux. Such an ocean would be energetically hospitable for terrestrial marine macrofauna. The availability of reductants could be the limiting factor for biologically useful chemical energy on Europa.     

Infrared spectra and radiation stability of H2O2 ices relevant to Europa

In this paper we present spectra of H2O2-containing ices in the near- and mid-infrared (IR) regions. Spectral changes on warming are shown, as is a comparison of near-IR bands of H2O and H2O2-containing ices. An estimate of the A-value (absolute intensity) for the largest near- IR feature of H2O2 is given. Radiation-decay half-lives are reported for 19 K and 80 K, and are related to the surface radiation doses on Europa. The radiation data show that H2O2 destruction is slower at 80 K than 19 K, and are consistent with the claim that icy material in the outermost micrometer of Europa's surface has been heavily processed by radiation.     

Clathrate hydrates of oxidants in the ice shell of Europa

Europa's icy surface is radiolytically modified by high-energy electrons and ions, and photolytically modified by solar ultraviolet photons. Observations from the Galileo Near Infrared Mapping Spectrometer, ground-based telescopes, the International Ultraviolet Explorer, and the Hubble Space Telescope, along with laboratory experiment results, indicate that the production of oxidants, such as H2O2, O2, CO2, and SO2, is a consequence of the surface radiolytic chemistry. Once created, some of the products may be entrained deeper into the ice shell through impact gardening or other resurfacing processes. The temperature and pressure environments of regions within the europan hydrosphere are expected to permit the formation of mixed clathrate compounds. The formation of carbon dioxide and sulfur dioxide clathrates has been examined in some detail. Here we add to this analysis by considering oxidants produced radiolytically on the surface of Europa. Our results indicate that the bulk ice shell could have a approximately 1.7-7.6% by number contamination of oxidants resulting from radiolysis at the surface. Oxidant-hosting clathrates would consequently make up approximately 12-53% of the ice shell by number relative to ice, if oxidants were entrained throughout. We examine, in brief, the consequences of such contamination on bulk ice shell thickness and find that clathrate formation could lead to substantially thinner ice shells on Europa than otherwise expected. Finally, we propose that double occupancy of clathrate cages by O2 molecules could serve as an explanation for the observation of condensed-phase O2 on Europa. Clathrate-sealed, gas-filled bubbles in the near surface ice could also provide an effective trapping mechanism, though they cannot explain the 5771 A (O2)2 absorption.     

火星探测用金属/CO2燃烧技术研究进展与展望

火星原位资源利用指利用火星当地资源生产火星探测所需原料和能源,减少任务载荷,降低发射成本,是火星探测不可或缺的关键技术。金属和二氧化碳是火星重要的原位资源,部分金属可以在二氧化碳气氛中燃烧,使得金属/CO_2燃烧体系在火星上扮演地球上化石燃料/空气燃烧体系的角色成为可能。从拓展金属/CO_2燃烧技术在火星探测中应用的角度出发,梳理了火星二氧化碳收集方式、火星矿物分布和冶炼、金属/CO_2燃烧技术的主要应用方式(Mg/CO_2火箭发动机和Mg/CO_2金属燃烧器)的研究进展,并对今后的研究进行了展望。     

Amino acids from ion-irradiated nitrile-containing ices

Solid CH(3)CN and solid H(2)O + CH(3)CN were ion irradiated near 10 K to initiate chemical reactions thought to occur in extraterrestrial ices. The infrared spectra of these samples after irradiation revealed the synthesis of new molecules. After the irradiated ices were warmed to remove volatiles, the resulting residual material was extracted and analyzed. Both unhydrolyzed and acid-hydrolyzed residues were examined by both liquid and gas chromatographic-mass spectral methods and found to contain a rich mixture of products. The unhydrolyzed samples showed HCN, NH(3), acetaldehyde (formed by reaction with background and atmospheric H(2)O), alkyamines, and numerous other compounds, but no amino acids. However, reaction products in hydrolyzed residues contained a suite of amino acids that included some found in carbonaceous chondrite meteorites. Equal amounts of D- and L-enantiomers were found for each chiral amino acid detected. Extensive use was made of (13)C-labeled CH(3)CN to confirm amino acid identifications and discriminate against possible terrestrial contaminants. The results reported here show that ices exposed to cosmic rays can yield products that, after hydrolysis, form a set of primary amino acids equal in richness to those made by other methods, such as photochemistry.     

Hydrogen emission in meteors as a potential marker for the exogenous delivery of organics and water

We detected hydrogen Balmer-alpha (H(alpha)) emission in the spectra of bright meteors and investigated its potential use as a tracer for exogenous delivery of organic matter. We found that it is critical to observe the meteors with high enough spatial resolution to distinguish the 656.46 nm H(alpha) emission from the 657.46 nm intercombination line of neutral calcium, which was bright in the meteor afterglow. The H(alpha) line peak stayed in constant ratio to the atmospheric emissions of nitrogen during descent of the meteoroid. If all of the hydrogen originates in the Earth's atmosphere, the hydrogen atoms are expected to have been excited at T = 4400 K. In that case, we measured an H(2)O abundance in excess of 150 +/- 20 ppm at 80-90 km altitude (assuming local thermodynamic equilibrium in the air plasma). This compares with an expected <20 ppm from H(2)O in the gas phase. Alternatively, meteoric refractory organic matter (and water bound in meteoroid minerals) could have caused the observed H(alpha) emission, but only if the line is excited in a hot T approximately 10000 K plasma component that is unique to meteoric ablation vapor emissions such as Si(+). Assuming that the Si(+) lines of the Leonid spectrum would need the same hot excitation conditions, and a typical [H]/[C] = 1 in cometary refractory organics, we calculated an abundance ratio [C]/[Si] = 3.9 +/- 1.4 for the dust of comet 55P/Tempel-Tuttle. This range agreed with the value of [C]/[Si] = 4.4 measured for comet 1P/Halley dust. Unless there is 10 times more water vapor in the upper atmosphere than expected, we conclude that a significant fraction of the hydrogen atoms in the observed meteor plasma originated in the meteoroid.     

90 keV电子辐照对Kapton H薄膜化学结构的影响

文章研究了能量为90 keV的电子辐照对Kapton H薄膜化学结构的影响。XPS分析表明,低能电子辐照导致Kapton H薄膜分子结构中C—N和C—O键的断裂,以及C＝O键的断裂和重组,并且有部分键断裂后交联。随着辐照剂量及辐照能量的增加,材料中的C—N、C＝O键含量减少,形成表面碳富集。辐照使柔性结构C—O键被破坏,产生的交联及以苯环为主的三维立体网状结构使其表面硬度增加。     

Nucleobases and prebiotic molecules in organic residues produced from the ultraviolet photo-irradiation of pyrimidine in NH(3) and H(2)O+NH(3) ices

Although not yet identified in the interstellar medium (ISM), N-heterocycles including nucleobases-the information subunits of DNA and RNA-are present in carbonaceous chondrites, which indicates that molecules of biological interest can be formed in non-terrestrial environments via abiotic pathways. Recent laboratory experiments and ab initio calculations have already shown that the irradiation of pyrimidine in pure H(2)O ices leads to the formation of a suite of oxidized pyrimidine derivatives, including the nucleobase uracil. In the present work, NH(3):pyrimidine and H(2)O:NH(3):pyrimidine ice mixtures with different relative proportions were irradiated with UV photons under astrophysically relevant conditions. Liquid- and gas-chromatography analysis of the resulting organic residues has led to the detection of the nucleobases uracil and cytosine, as well as other species of prebiotic interest such as urea and small amino acids. The presence of these molecules in organic residues formed under abiotic conditions supports scenarios in which extraterrestrial organics that formed in space and were subsequently delivered to telluric planets via comets and meteorites could have contributed to the inventory of molecules that triggered the first biological reactions on their surfaces.     

Oxidant enhancement in martian dust devils and storms: implications for life and habitability

We investigate a new mechanism for producing oxidants, especially hydrogen peroxide (H2O2), on Mars. Large-scale electrostatic fields generated by charged sand and dust in the martian dust devils and storms, as well as during normal saltation, can induce chemical changes near and above the surface of Mars. The most dramatic effect is found in the production of H2O2 whose atmospheric abundance in the "vapor" phase can exceed 200 times that produced by photochemistry alone. With large electric fields, H2O2 abundance gets large enough for condensation to occur, followed by precipitation out of the atmosphere. Large quantities of H2O2 would then be adsorbed into the regolith, either as solid H2O2 "dust" or as re-evaporated vapor if the solid does not survive as it diffuses from its production region close to the surface. We suggest that this H2O2, or another superoxide processed from it in the surface, may be responsible for scavenging organic material from Mars. The presence of H2O2 in the surface could also accelerate the loss of methane from the atmosphere, thus requiring a larger source for maintaining a steady-state abundance of methane on Mars. The surface oxidants, together with storm electric fields and the harmful ultraviolet radiation that readily passes through the thin martian atmosphere, are likely to render the surface of Mars inhospitable to life as we know it.     

The catalytic potential of cosmic dust: implications for prebiotic chemistry in the solar nebula and other protoplanetary systems

The synthesis of important prebiotic molecules is fundamentally reliant on basic starting ingredients: water, organic species [e.g., methane (CH(4))], and reduced nitrogen compounds [e.g., ammonia (NH(3)), methyl cyanide (CH(3)CN) etc.]. However, modern studies conclude that the primordial Earth's atmosphere was too rich in CO, CO(2), and water to permit efficient synthesis of such reduced molecules as envisioned by the classic Miller-Urey experiment. Other proposed sources of terrestrial nitrogen reduction, like those within submarine vent systems, also seem to be inadequate sources of chemically reduced C-H-O-N compounds. Here, we demonstrate that nebular dust analogs have impressive catalytic properties for synthesizing prebiotic molecules. Using a catalyst analogous to nebular iron silicate condensate, at temperatures ranging from 500K to 900K, we catalyzed both the Fischer-Tropsch conversion of CO and H(2) to methane and water, and the corresponding Haber-Bosch synthesis of ammonia from N(2) and H(2). Remarkably, when CO, N(2), and H(2) were allowed to react simultaneously, these syntheses also yielded nitrogen-containing organics such as methyl amine (CH(3)NH(2)), acetonitrile (CH(3)CN), and N-methyl methylene imine (H(3)CNCH(2)). A fundamental consequence of this work for astrobiology is the potential for a natural chemical pathway to produce complex chemical building blocks of life throughout our own Solar System and beyond.     

Detectability of planetary characteristics in disk-averaged spectra. I: The Earth model

Over the next 2 decades, NASA and ESA are planning a series of space-based observatories to detect and characterize extrasolar planets. This first generation of observatories will not be able to spatially resolve the terrestrial planets detected. Instead, these planets will be characterized by disk-averaged spectroscopy. To assess the detectability of planetary characteristics in disk-averaged spectra, we have developed a spatially and spectrally resolved model of the Earth. This model uses atmospheric and surface properties from existing observations and modeling studies as input, and generates spatially resolved high-resolution synthetic spectra using the Spectral Mapping Atmospheric Radiative Transfer model. Synthetic spectra were generated for a variety of conditions, including cloud coverage, illumination fraction, and viewing angle geometry, over a wavelength range extending from the ultraviolet to the farinfrared. Here we describe the model and validate it against disk-averaged visible to infrared observations of the Earth taken by the Mars Global Surveyor Thermal Emission Spectrometer, the ESA Mars Express Omega instrument, and ground-based observations of earthshine reflected from the unilluminated portion of the Moon. The comparison between the data and model indicates that several atmospheric species can be identified in disk-averaged Earth spectra, and potentially detected depending on the wavelength range and resolving power of the instrument. At visible wavelengths (0.4-0.9 microm) O3, H2O, O2, and oxygen dimer [(O2)2] are clearly apparent. In the mid-infrared (5-20 microm) CO2, O3, and H2O are present. CH4, N2O, CO2, O3, and H2O are visible in the near-infrared (1-5 microm). A comprehensive three-dimensional model of the Earth is needed to produce a good fit with the observations.     

真空羽流气相沉积污染初步研究

从固体表面对气体分子的作用着手分析气相羽流沉积污染的内在机理,阐述了固体表面对气体分子的物理吸附、化学吸附特性,给出吸附速率方程、脱附速率方程以及沉积速率方程,并通过区分贴壁吸附层、物理吸附层,重点研究了物理吸附层的脱附速率。选取有代表性的CO₂、NH₃、H₂O以及N₂H₄等气体,确定其物理吸附层脱附模型的参数,得到了与经验脱附率曲线较为一致的理论脱附率曲线。分析了单组元肼催化分解姿控发动机对太阳能帆板的气相沉积污染。     

Cyanobacterial emergence at 2.8 gya and greenhouse feedbacks

Apparent cyanobacterial emergence at about 2.8 Gya coincides with the negative excursion in the organic carbon isotope record, which is the first strong evidence for the presence of atmospheric methane. The existence of weathering feedbacks in the carbonate-silicate cycle suggests that atmospheric and oceanic CO2 concentrations would have been high prior to the presence of a methane greenhouse (and thus the ocean would have had high bicarbonate concentrations). With the onset of a methane greenhouse, carbon dioxide concentrations would decrease. Bicarbonate has been proposed as the preferred reductant that preceded water for oxygenic photosynthesis in a bacterial photosynthetic precursor to cyanobacteria; with the drop of carbon dioxide level, Archean cyanobacteria emerged using water as a reductant instead of bicarbonate (Dismukes et al., 2001). Our thermodynamic calculations, with regard to this scenario, give at least a tenfold drop in aqueous CO2 levels with the onset of a methane-dominated greenhouse, assuming surface temperatures of about 60 degrees C and a drop in the level of atmospheric carbon dioxide from about 1 to 0.1 bars. The buildup of atmospheric methane could have been triggered by the boost in oceanic organic productivity that arose from the emergence of pre-cyanobacterial oxygenic phototrophy at about 2.8-3.0 Gya; high temperatures may have precluded an earlier emergence. A greenhouse transition timescale on the order of 50-100 million years is consistent with results from modeling the carbonate-silicate cycle. This is an alternative hypothesis to proposals of a tectonic driver for this apparent greenhouse transition.     

CVI沉积炭纤维束的组织结构

采用CVI工艺在常压下对单束炭纤维进行热解沉积,天然气为前驱体,N2为载气,沉积温度为1 020～1 100℃,沿纤维束轴向分布。对不同位置炭纤维束外和束内热解炭组织结构分别进行PLM表征。研究发现,束外热解炭在距离热电偶(0位置)上方40～80 mm处沉积厚度达到最大,在0～80 mm内组织结构良好,主体为高织构;束内沉积热解炭的厚度较均匀,组织结构的变化与束外一致。对气体裂解过程中的反应气体组分进行模拟并与实验对比,发现生成高织构时,热解反应中间产物中的C2H2/C6H6范围为15～35。     

Formaldehyde in the far outer galaxy: constraining the outer boundary of the galactic habitable zone

We present results from an initial survey of the 2(12)-1(11) transition of formaldehyde (H2CO) at 140.8 GHz in giant molecular clouds in the far outer Galaxy (RG >or= 16 kpc). Formaldehyde is a key prebiotic molecule that likely plays an important role in the development of amino acids. Determining the outermost extent of the H2CO distribution can constrain the outer limit of the Galactic Habitable Zone, the region where conditions for the formation of life are thought to be most favorable. We surveyed 69 molecular clouds in the outer Galaxy, ranging from 12 to 23.5 kpc in galactocentric radius. Formaldehyde emission at 140.8 GHz was detected in 65% of the clouds. The H2CO spectral line was detected in 26 of the clouds with RG > 16 kpc (detection rate of 59%), including 6 clouds with RG > 20 kpc (detection rate of 55%). Formaldehyde is readily found in the far outer Galaxy-even beyond the edge of the old stellar disk. Determining the relatively widespread distribution of H2CO in the far outer Galaxy is a first step in establishing how favorable an environment this vast region of the Galaxy may be toward the formation of life.     

Oxidant enhancement in martian dust devils and storms: storm electric fields and electron dissociative attachment

Laboratory studies, numerical simulations, and desert field tests indicate that aeolian dust transport can generate atmospheric electricity via contact electrification or "triboelectricity." In convective structures such as dust devils and dust storms, grain stratification leads to macroscopic charge separations and gives rise to an overall electric dipole moment in the aeolian feature, similar in nature to the dipolar electric field generated in terrestrial thunderstorms. Previous numerical simulations indicate that these storm electric fields on Mars can approach the ambient breakdown field strength of approximately 25 kV/m. In terrestrial dust phenomena, potentials ranging from approximately 20 to 160 kV/m have been directly measured. The large electrostatic fields predicted in martian dust devils and storms can energize electrons in the low pressure martian atmosphere to values exceeding the electron dissociative attachment energy of both CO2 and H2O, which results in the formation of the new chemical products CO/O- and OH/H-, respectively. Using a collisional plasma physics model, we present calculations of the CO/O- and OH/H- reaction and production rates. We demonstrate that these rates vary geometrically with the ambient electric field, with substantial production of dissociative products when fields approach the breakdown value of approximately 25 kV/m. The dissociation of H2O into OH/H- provides a key ingredient for the generation of oxidants; thus electrically charged dust may significantly impact the habitability of Mars.     

Analysis of an algae-based CELSS. Part 1: model development

A steady state chemical model and computer program have been developed for a life support system and applied to trade-off studies. The model is based on human demand for food and oxygen determined from crew metabolic needs. The model includes modules for water recycle, waste treatment, CO2 removal and treatment, and food production. The computer program calculates rates of use and material balance for food. O2, the recycle of human waste and trash, H2O, N2, and food production supply. A simple non-iterative solution for the model has been developed using the steady state rate equations for the chemical reactions. The model and program have been used in system sizing and subsystem trade-off studies of a partially closed life support system.     

硅橡胶基绝热材料高温热行为研究

采用高温管式炉在惰性气氛下研究了硅橡胶基绝热材料在1 073～1 873 K的热行为,利用X射线衍射和红外光谱等手段探索了高温固相残余物的产生历程和碳化硅的生成机制,采用热重-差热联用表征了高温固相残余物的热氧化性能。研究结果表明,随着处理温度升高,硅橡胶基绝热材料的固相残余物逐渐向高温陶瓷转化,其热稳定性和耐氧化性相应提高;硅橡胶基体在1 073 K已分解完毕,其固相残余物为碳、硅氧碳化物和SiO2等;随温度上升,有机碳向更加耐氧化的无机碳转变;硅氧碳化物随温度升高向碳化硅转化;气相SiO2高温下由无定型转化为方石英晶体,并与碳发生碳热反应生成碳化硅。     

质子和离子辐照对镁稀土合金 力学性能的影响

文章研究了质子和离子（氮离子）辐照对镁稀土（Mg-Zn-Y-Zr）合金拉伸性能、表面硬度及拉伸变形断裂行为的影响。经能量为170 keV,注量分别为5×1015 /cm2、1×1016 /cm2、2×1016 /cm2、1×1017 /cm2的质子或离子辐照后,合金的拉伸性能和拉伸断口形貌没有发生显著变化,表明质子和离子辐照对Mg-Zn-Y-Zr合金宏观力学性能的影响有限,这与辐照粒子（质子或离子）对合金的穿透深度浅有关。纳米显微硬度测试和扫描分析结果显示,经氮离子辐照后,Mg-Zn-Y-Zr合金被辐照面表层发生了一定程度的硬化,纳米显微硬度随着辐照注量的增加而逐渐增加,而质子辐照的硬化效果不明显。