A photo-chemical method for the production of olivine nanoparticles as cosmic dust analogues

被引:35
作者
Saunders, Russell W. [1 ]
Plane, John M. C. [1 ]
机构
[1] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
基金
英国自然环境研究理事会;
关键词
Meteors; Atmospheres; Chemistry; Earth; Mineralogy; INTERSTELLAR SILICATE MINERALOGY; OPTICAL-PROPERTIES; CHEMISTRY; CONDENSATION; MAGNESIUM; EVOLUTION; ABLATION; GRAINS; STEPS; VAPOR;
D O I
10.1016/j.icarus.2010.12.019
中图分类号
P1 [天文学];
学科分类号
0704 ;
摘要
This paper describes a new experimental method to synthesise metal silicate particles in the laboratory with compositions and structures which reflect those likely to form in planetary atmospheres and in relatively cool regions of oxygen-rich stellar outflows. Fe-Mg-silicate nanoparticles of olivine composition were produced by the photo-oxidation of a mixture of Fe(CO)(5), Mg(OC2H5)(2) and Si(OC2H5)(4) vapours in the presence of O-3 at room temperature and atmospheric pressure. Transmission electron microscope X-ray and electron energy loss analysis of the particles from a number of experiments run with different precursor vapour mixture ratios show that Mg2xFe2-2x SiO4 particles can be produced ranging from x = 0 to 1, where x is linearly proportional to the ratio of Mg(OC2H5)(2)/(Fe(CO)(5) + Mg(OC2H5)(2)). Electronic structure calculations with hybrid density functional/Hartree-Fock theory are then used to explore the pathways involved in producing olivine particles from the FeO3, MgO3 and SiO2 produced from the photolysis of the organometallic precursors in O-3. These calculations indicate that highly exothermic reactions lead to the formation of Mg2SiO4, MgFeSiO4 and Fe2SiO4 molecules, which then polymerize. An alternative pathway, also strongly favoured thermodynamically, is the polymerization of MgSiO3 and FeSiO3 to form pyroxenes, which then undergo structural rearrangement to olivine and silica phases. The implications for metal silicate formation in planetary atmosphere and stellar outflows are then discussed. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:373 / 382
页数:10
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