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Figure 1:
Sketch of the surface chemical processes involved in the
growth and evaporation of an island of solid material s at the
surface of a dirty dust grain. The total surface area
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Figure 2:
Local hydro- and thermodynamical processes in a dust-forming gas
as affected by expansion waves (dashed : 0.01 s, solid: 0.15 s, dotted: 5 s).
1st row: l.h.s. density |
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Figure 3:
Local details of the dust formation process and the
evolution of the chemical abundances in the gas phase. The
colours/line-styles indicate the dust species (and assigned elements) as
follows. Dark blue/full: TiO2[s] (Ti); brown/short
dash-dot: SiO2[s] (Si); green/long dash-dot: Fe[s] (Fe);
orange/long dashed: Mg2SiO4[s] (Mg), light blue/dotted:
Al2O3[s] (Al); red/dashed: [no assigned dust species] (O).
1st row: supersaturation ratios S (*), 2nd row: inverse surface
area non-equilibrium factors
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Figure 4:
Dust volume fractions, expressed by
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Figure 5:
Gas phase chemistry: particle densities |
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Figure 6:
Evolution of temperature, dust, and chemistry at the centre
of wave interaction (x=0.25, l.h.s.: short-term - r.h.s.: long-term).
Left panels on l.h.s.:
1st row: temperature T [1900 K],
2nd row: nucleation rate per hydrogen nuclei
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Figure 7:
Same as l.h.s of Figs. 6 and 4, but for
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Figure 8:
Influence of reaction kinetics on the cumulative volume fraction
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Figure B.1:
Thought experiment to obtain the reference state |