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    Spectra

    Original: Michael Balogh, Univ. Waterloo

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    Stellar spectraStellar spectra show interesting trends as a function of temperature:

    Increasingtemperature

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    Review: spectral classesSpectral

    Type

    Colour Temperature

    (K)

    Main characteristics Example

    O Blue-white >25000 Strong HeII absorption (sometimesemission); strong UV continuum

    10 Lacertra

    B Blue-white 11000-25000 HeI absorption, weak Balmer lines Rigel

    A White 7500-11000 Strongest Balmer lines (A0) Sirius

    F Yellow-white 6000-7500 CaII lines strengthen Procyon

    G Yellow 5000-6000 Solar-type spectra Sun

    K Orange 3500-5000 Strong metal lines Arcturus

    M Red

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    The HR diagram revisited

    Henry Norris original diagram, showing stellar

    luminosity as a function of spectral class.

    The main sequence is clearly visible

    Spectral Class

    O B A F G K M

    Luminosity

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    Luminosity class

    The lumino s i ty c lassis assigned a roman numeral: I II III

    IV V or VI and is related to the width of the spectral linewhich we will see is related to the stellar luminosity

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    Spectroscopic parallax

    In principle, you can identify both

    the spectral class and theluminosity class from the spectrum.

    It is therefore possible to locate

    the stars position on the HR

    diagram and determine its

    absolute magnitude. This can be

    used to determine the distance to

    the star. This method is known as

    spectroscopic parallax

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    Example

    The star Rigel has a spectral type B8Ia and a magnitude

    V=0.14. What is its distance?

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    Kirchoffs laws

    1. A hot, dense gas or hot solid object

    produces a continuous spectrum with no

    dark spectral lines

    2. A hot, diffuse gas produces bright spectral

    emiss ion l ines

    3. A cool, diffuse gas in front of a source of acontinuous spectrum produces dark

    absorpt ion l inesin the continuous

    spectrum

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    Review: The hydrogen atom

    eV6.132n

    En

    where n is the principal quantumnumber.

    2

    1

    2

    2

    21

    116.13

    nn

    eVEEE

    2

    1

    2

    2

    11

    16.91

    11

    nnnm

    The change in energy is

    associated with the

    absorption or emission of aphoton. For Hydrogen:

    Thus the energy difference between twoorbitals n1 and n2 of Hydrogen is givenby:

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    The Boltzmann factor

    The probability that an electron is

    in a given energy level dependson the Boltzmann factor:

    kTEE

    kT

    E

    kT

    E

    a

    bab

    a

    b

    e

    e

    e

    sP

    sP

    )(

    )(

    kT

    E

    e

    Thus the ratio of the probability that an electron is in state sb to the probabilitythat it is in state sa is just:

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    1. n is the principal quantum

    number related to the

    energy of the orbital

    2. The angular momentum is

    quantized to have values of

    3. The z-component of angularmomentum can only have

    values of

    where mlis an integer

    betweenland l

    The quantum atom

    Electron probability distributions are described by orbitals that

    are specified by three quantum numbers:n l m

    l

    )1( llL

    lz mL

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    1. is the principal quantum

    number related to the

    energy of the orbital

    2. The angular momentum is

    quantized to have values of

    3. The z-component of angularmomentum can only have

    values of

    where mlis an integer

    betweenland l

    The quantum atom

    Electron probability distributions are described by orbitals that

    are specified by three quantum numbers:n l m

    l

    )1( llL

    lz mL

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    1. n is the principal quantum

    number related to the

    energy of the orbital

    2. The angular momentum is

    quantized to have values

    of

    3. The z-component of angular

    momentum can only have

    values of

    where mlis an integer

    betweenland l

    The quantum atom

    Electron probability distributions are described by orbitals that

    are specified by three quantum numbers:n l m

    l

    )1( llL

    lz mL

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    1. n is the principal quantum

    number related to the

    energy of the orbital

    2. The angular momentum is

    quantized to have values of

    3. The z-component ofangular momentum can

    only have values of

    where ml

    is an integer

    between

    l and l

    The quantum atom

    Electron probability distributions are described by orbitals that

    are specified by three quantum numbers:n l m

    l

    )1( llL

    lz mL

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    Degeneracies

    There may be more than one state with the same energyE. For example, for an isolated Hydrogen atom thequantum numbers associated with spin and angularmomentum do not affect the energy

    kT

    EE

    a

    bab

    esP

    sP

    )(

    )(

    n l ml

    ms

    E (eV)

    1 0 0 +1/2 -13.6

    1 0 0 -1/2 -13.6

    2 0 0 +1/2 -3.4

    2 0 0 -1/2 -3.4

    2 1 0 +1/2 -3.42 1 0 -1/2 -3.4

    2 1 1 +1/2 -3.4

    2 1 1 -1/2 -3.4

    2 1 -1 +1/2 -3.4

    2 1 -1 -1/2 -3.4

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    Degeneracies

    Therefore the probability that a system will be found in any state with energy Eb,

    relative to the probability that it will be found in any state with energy Ea is:

    kT

    EE

    a

    b

    kT

    E

    a

    kT

    E

    b

    a

    bab

    a

    b

    eg

    g

    eg

    eg

    EP

    EP

    )(

    )( n l ml ms E(eV)

    1 0 0 +1/2 -13.6

    1 0 0 -1/2 -13.6

    2 0 0 +1/2 -3.4

    2 0 0 -1/2 -3.4

    2 1 0 +1/2 -3.4

    2 1 0 -1/2 -3.4

    2 1 1 +1/2 -3.4

    2 1 1 -1/2 -3.4

    2 1 -1 +1/2 -3.4

    2 1 -1 -1/2 -3.4

    For the Hydrogen atom only, the degeneracy

    depends on the energy level n like:

    22)( nng

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    The Boltzmann equation

    Since the number of atoms in stellar atmospheres is so large, the ratio ofprobabilities is essentially equal to the ratio of atoms in each state. This is the

    Bol tzmann equat ion:

    kT

    EE

    a

    b

    a

    bab

    eg

    g

    N

    N

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    Example

    For a gas of neutral Hydrogen atoms at room temperature,

    what is the ratio of the number of electrons in the n=2state to the number in the n=1 state?

    What temperature do you need to get a significant number

    (say 10%) of electrons into the n=2 state (for a neutral

    Hydrogen gas)?

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    Puzzling

    The Balmer sequence of absorption lines is due to the transition from n=2 ton>2.

    The strength of the Balmer lines is largest for A0 stars, which havetemperatures ~9520 K

    But we just found you need temperatures ~3 times larger than this to get even10% of electrons into the n=2 state; and this n=2 population will increasefurther with increasing temperature.

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    Break

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    Ionization

    So far we have just dealt with neutralatoms. However, if

    the temperature gets high enough, electrons can beentirely removed from the atom.

    Lets define ci to be the energy required to remove an electron from an

    atom. This increases its ionization state from i to i+1

    Eg. It takes 13.6 eV of energy to remove an electron in the ground stateof Hydrogen. So cI=13.6 eV.

    Ionization states are usually denoted by Roman numerals. So the

    neutral hydrogen atom is HI and the first ionization state is HII and so

    on.

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    Partition functions

    We want to compute the number of atoms in ionization state i+1 relative to the

    number in ionization state i.

    To do this we need to sum over all possible orbital distributions of each state.

    i.e. how could the electrons be distributed in each ionization state?

    The sum of the number of configurations, weighted by the probability of each

    configuration, is thepartition function:

    kT

    EE

    j

    j

    j

    eggZ1

    2

    1

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    The Saha Equation

    In 1920, Meghnad Saha derived an equation for the relative number of

    atoms in each ionization state. Well just present the result:

    kTe

    ie

    i

    i

    ii

    eh

    kTm

    Zn

    Z

    N

    N c

    2/3

    2

    11 22

    Note:

    This depends on the number density of electrons, ne. This is because

    as the number of free electrons increases, it is more likely that they can

    recombine with an atom and lower the ionization state.

    The Boltzmann factor exp(-ci/kT) means it is more difficult to ionize

    atoms with high ionization potentials

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    Example: typical Hydrogen atmospheres

    4

    16.1

    2/3

    4

    1

    320

    171

    m101083.4 Te

    i

    i

    i

    i

    i

    eT

    n

    Z

    Z

    N

    N c

    32010

    eV6.13

    mne

    Ic

    Evaluate the partition functions

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    Example: typical Hydrogen atmospheres

    4

    16.1

    2/3

    4

    1

    320

    171

    m101083.4 Te

    i

    i

    i

    i

    i

    eT

    n

    Z

    Z

    N

    N c

    32010

    eV6.13

    mne

    Ic

    Evaluate the partition functions

    Hydrogen has only one electron, so there is only HI (neutral) and HII (ionized).

    HII is just a proton: there is only one state, so Z II=1

    We saw that, for T

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    Example: typical Hydrogen atmospheres

    4/11777.152/344.3

    T

    I

    II eT

    N

    N

    T(K) T4 NII/NI NII/(NI+NII)

    5500 0.55 3.410-6 3.410-6

    8000 0.8 0.047 0.0459000 0.9 0.50 0.33

    10000 1 3.4 0.77

    15000 1.5 1201 0.9992

    20000 2 25640 0.99996

    where T4 =T/(10,000K)

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    Example: typical Hydrogen atmospheres

    In the interior of stars, temperature decreases from the core to the surface. The narrowregion inside a star where Hydrogen is partially ionized is called the hydrogen part ial

    ionizat ion zone

    Ionization fraction as a

    function of temperaturefor 3 different electron

    densities:

    ne=1021 m-3

    ne=1020 m-3

    ne=1019 m-3

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    Balmer line formation

    Calculate the relative strength of the Balmer absorption

    lines as a function of temperature

    IIItotal NNNNNN

    /1)1/(

    1

    21

    2

    T N1/N2 NII/NI N2/Ntotal

    4000 1.6x1012 4.3x10-11 6.2x10-13

    5000 4.4x10

    9

    1.6x10

    -7

    2.3x10

    -10

    9000 1.2x105 0.50 5.5x10-6

    15000 652 1203 1.3x10-6

    20000 91 2.6x104 4.2x10-7

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    Balmer line formation

    This shows why Balmer lines are strongest at ~9000 K.

    They quickly get weaker at higher temperatures becausethe ionization fraction increases.

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    Boltzmann and Saha equations: applicability

    Saha equation depends on electron density

    10% of the atoms in a real star are Helium. Ionized Heliumincreases ne, and therefore decreases the ionization fraction of

    H at a fixed temperature

    These equations only apply if the gas is in thermal

    equilibrium

    The energy levels of H were calculated for an isolated

    atom. If the gas density gets too large (~1 kg/m3) this is

    no longer a good approximation, and the ionization

    energy becomes lower than 13.6 eV.

    (recall the average density in the Sun is ~1410 kg/m3)

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    Example: Calcium lines in the Sun

    The Calcium absorption lines are ~400 times stronger than theHydrogen lines. How much Calcium is there, relative to Hydrogen?

    Assume ne=1.88x1019 m-3 and T=5770 K

    First, lets look at hydrogen. The Balmer lines arise due to transitionsfrom the n=2 level of neutral H.

    Ca H+K

    5

    777.15

    2/3

    4

    1

    320

    7

    1051.7

    m101083.4 4

    Te

    I

    II

    I

    II eTn

    Z

    Z

    N

    N

    So almost all the Hydrogen is

    neutral.

    Ha

    9

    1

    1

    2

    1

    577.0

    777.152

    11777.152

    1

    2

    1096.4

    1

    2 22

    21

    224

    1

    2

    e

    en

    n

    N

    NnnT

    n

    n

    So only 1 of every ~200 million H atoms is in the

    first excited state (and capable of creating aBalmer absorption line).

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    Example: Calcium lines in the Sun

    The Calcium absorption lines are ~400 times stronger than the Hydrogen lines.

    How much Calcium is there, relative to Hydrogen? Assume ne=1.88x1019 m-3

    and T=5770 K

    For Hydrogen:

    The partition functions are more complicated to compute, so Ill just give them to

    you: ZI=1.32 and ZII=2.3

    The =393.3 nm Calcium line in the sun come from the n=12

    transition of singly-ionized calcium.

    51051.7 I

    II

    N

    N 91096.4

    1

    2 n

    n

    N

    N

    Now consider Calcium, for which cI=6.11 eV

    For the Boltzmann equation, I tell you that for singly ionized Calcium 4and2 21 gg

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    Example: Calcium lines in the Sun

    The Calcium absorption lines are ~400 times stronger than the Hydrogen lines. How

    much Calcium is there, relative to Hydrogen? Assume ne=1.88x1013 and T=5770 K

    There is only one Ca atom for every 520,000 H atoms.

    The difference: Ca is easier to ionize than H (cI=6.11 instead of 13.6), and

    Ca has more than 1 electron, so is able to emit radiation in the singly-

    ionized state!

    We have found that only 4.8x10-9 of H atoms are in the first excited state (to produce

    Balmer lines), whereas 99.5% of Ca atoms are in the ground, singly-ionized state (to

    produce the solar absorption lines).

    Since the Ca lines are ~400 times stronger, this means:

    HCa

    H

    Ca

    NN

    N

    N

    6

    9

    100.2

    4001096.4

    995.0


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