Approach to Nucleation in Astronomical Environments

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Presentation transcript:

Approach to Nucleation in Astronomical Environments 2012/01/16 Approach to Nucleation in Astronomical Environments Takaya Nozawa (野沢 貴也) Institute for the Physics and Mathematics of the Universe (IPMU), University of Tokyo

1-1. Introduction Cosmic dust universally exits in space when, where, and how is dust formed? Properties of dust evolves through the processing in the ISM (sputtering, shattering, coagulation, growth ..) composition, size, and amount of newly formed dust extinction curve IR spectral feature depletion of elements

1-2. Formation sites of dust when, where, and how is dust formed? in cooling gas outflows ・ abundant metals (metal: atomic number > 5) ・ low gas temperature (T < ~2000 K) ・ high gas density (n > ~106 cm-3) possible formation sites of dust - expanding ejecta of supernovae - mass-loss winds of AGB stars - molecular clouds (grain growth only) what kinds of, what size of, how much dust is formed

1-3. Missing-dust problem in CCSNe Matsuura, ..., TN, et al. 2011, Science by courtesy of M. Tanaka cool dust in SN1987A theory cold dust ?? young SNRs young SNe Herschel detects cool (20K) dust of 0.4-0.7 Msun toward SN 1987A! There is a big difference in the mass of dust between observational estimates and theoretical predictions!!

2-1. How do dust grains form? gaseous atoms chemical approach nucleation approach molecules formation of seed nuclei ??? large molecules dust grains

2-2. Supersaturation ratio Tdust is assumed to equal to T=Tgas ① ・ supersaturation ratio, S ➔ ratio of real partial pressure to equilibrium partial pressure gaseous atom c1 Pe,1 P1 For condensation of dust, S = P1 / Pe,1 > 1 ➔ lnS = ln(P1 / Pe,1) > 0 solid (bulk) material lnS = A / T – B + ln(c1kT / P0) where –ΔG0/kT = A/T – B (A=8.64x104, B=19 for C grains) lnS is higher for lower T and higher c1

2-3. Behavior of supersaturation ratio increasing lnS lnS = A / T – B + ln(c1kT / P0) lnS is higher for lower T and higher c1 ・ number density of carbon atom to be lnS > 0 - c1 >~ 108 cm-3 at 2000 K - c1 >~ 106 cm-3 at 1800 K - c1 >~ 3x103 cm-3 at 1600 K

3-1. Concept of nucleation αnc1cn cn+1 J1 J2 Jn βncn+1 ・ Master equations dcn/dt = Jn-1 – Jn (n ≥ 2) Jn = αn c1 cn – βn cn+1 (unit of Jn : cm-3 s-1) αn = sn Sn <v> = sn 4πa02 n2/3 <v> βn = αn ce,1 (ce,n / ce,n+1) sn=1 is assumed for every n ③ coagulation between clusters is neglected small clusters are assumed to be spheres ② ④

3-2. Steady-state nucleation rate αnc1cn cn+1 J1 J2 Jn βncn+1 Jn = αnc1cn[1 – (ce,1/c1)(ce,n/cn)(cn+1/ce,n+1)] “steady” ➔ Js = J1 = J2 = ・・・ = Jn Js = {1/(α1c1) + ∑ (ce,1/c1)n 1/(αnc1ce,n+1)}-1 (ce,1/c1)n (1/ce,n+1) = (1/c1) exp [g(n)] where g(n) = μ(n-1)2/3 – (n-1)lnS ➔ Js = {1/(α1c1) + ∑ 1/(αnc12) exp[g(n)]}-1 ⑤

3-3. Critical radius Js = {1/(α1c1) + ∑ 1/(αnc12) exp[g(n)] }-1 g(n) = μ(n-1)2/3 –(n-1)lnS μ = 4πa02σ / kT (σ = 1400 erg cm-3 for C grains) The surface energy of small clusters is assumed to be the same as that of bulk ⑥ critical radius

3-4. Critical radius of nucleation ⑦ n* = 2 n* = n* – 1 assuming n* >> 1 Js = {1/(α1c1) + ∑ 1/(αnc12) exp[g(n)] }-1

3-5. Comparison of steady-state nucleation n* = n* – 1 assuming n* >> 1 reasonable !! ⑦ small n* ・ solid line : approximation formula for nucleation rate ・ dashed line : summation form for nucleation rate Js = {1/(α1c1) + ∑ 1/(αnc12) exp[g(n)] }-1

4-1. Non-steady nucleation rate Js = {1/(α1c1) + ∑ 1/(αnc12) exp[g(n)] }-1 “steady” ➔ Js = J1 = J2 = ・・・ = Jn Jn = αnc1cn[1 – (ce,1/c1)(ce,n/cn)(cn+1/ce,n+1)] ➔ Jn = αnc1 {cn – cn+1 exp[g’(n)]} g’(n) = μ [(n-1)2/3 – (n-2)2/3] – lnS ・ Master equations dcn/dt = Jn-1 – Jn (2 ≤ n ≤ 100) ⑤ T = T0 (t / t0)-3/4 (T0 = 3000 K, t0 = 150 day) c1 = c10 (t / t0)-3 (c10 = 105 – 108 cm-3)

4-2. Basic equations of dust formation Equation of conservation for atoms Equation of grain growth

4-3. Steady vs. Non-steady (1) c10 = 108 cm-3 c10 = 107 cm-3 ・ dashed line : steady-state nucleation rate ・ dotted line : non-steady-state nucleation rate The difference between steady and non-steady nucleation is small for higher initial densities

4-4. Steady vs. Non-steady (2) c10 = 106 cm-3 c10 = 105 cm-3 ・ dotted line : steady-state nucleation rate ・ dashed line : non-steady-state nucleation rate The difference between steady and non-steady nucleation is significant for lower densities

5-1. Relaxation time τcoll = [ sn 4πa02 <v> c1 ]-1 ・ relaxation time, τrelax ➔ τrelax = τcoll [ (lnS)2 / μ ] τcoll = [ sn 4πa02 <v> c1 ]-1 τrelax / τcoll = [ (lnS)2 / μ ] < 1 ➔ steady τrelax / τcoll = [ (lnS)2 / μ ] > 1 ➔ non-steady

5-2. Trajectories on T-c1 plot for dust formation ・ higher c1 ➔ dust condenses at lower lnS ➔ steady ・ lower c1 ➔ dust condenses at higher lnS ➔ non-steady

6. Current problems in dust formation theory ① Dust temperature is assumed to be equivalent to gas temperature ② The coagulation between clusters is neglected ③ The sticking probability is assumed to be one ④ Small clusters are assumed to be spherical ⑤ Js = J1 = J2 = ・・・ = Jn* for steady-state nucleation ⑥ The surface energy of bulk material is used as that of small clusters ⑦ n* >> 1 is assumed for classical nucleation rate ➔ this assumption is valid