FAST SCAN SUBMILLIMETER SPECTROSCOPIC TECHNIQUE FASSST' - PowerPoint PPT Presentation

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FAST SCAN SUBMILLIMETER SPECTROSCOPIC TECHNIQUE FASSST'

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IVAN R. MEDVEDEV, BRENDA P. WINNEWISSER, MANFRED WINNEWISSER, ... Freezes Source Frequency Drift. Freezes Chemistry Changes. 2. Frequency measurement accuracy ... – PowerPoint PPT presentation

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Title: FAST SCAN SUBMILLIMETER SPECTROSCOPIC TECHNIQUE FASSST'


1
FAST SCAN SUBMILLIMETER SPECTROSCOPIC TECHNIQUE
(FASSST). IVAN R. MEDVEDEV, BRENDA P.
WINNEWISSER, MANFRED WINNEWISSER, FRANK C. DE
LUCIA, DOUGLAS T. PETKIE, MARKUS BEHNKE, RYAN P.
A. BETTENS, and ZBIGNIEW KISIEL
2
Overview
  • TECHNIQUE
  • FAst Scan Submillimeter Spectroscopic Technique
    (FASSST).
  • Frequency measurements
  • CHALLENGES
  • Line intensity measurements
  • Spectral predictions without assignment or
    analysis

3
FAst Scan Submillimeter Spectroscopic Technique
(FASSST) spectrometer
Magnet
Mylar beam splitter 1
Glass rings used to suppress reflections
Lens
Reference gas cell
InSb detector 1
BWO
Lens
Aluminum cell length 6 m diameter 15 cm
Length 60 cm
Path of microwave radiation
Frequency roll-off preamplifier
Mylar beam splitter 2
Reference channel
InSb detector 2
Preamplifier
Interference fringes
Spectrum
Signal channel
Stepper motor
Data acquisition system Computer
Ring cavity L15 m
Stainless steel rails
Slow wave structure sweeper
Trigger channel /Triangular waveform channel
Filament voltage power supply
High voltage power supply
4
  • FASSST Attributes
  • 1. Can record 10000-100000 resolution
    elements/sec
  • Freezes Source Frequency Drift
  • Freezes Chemistry Changes
  • 2. Frequency measurement accuracy
  • Typically 30 kHz ( 1/107 at 300 GHz)
  • 3. Locally ( 1 GHz) intensity measurement
    is flat to 1
  • A basis for intensity measurement

5
Identification of the U lines in the
interstellar molecular spectra. Spectral
predictions without assignment or
analysis. Orion. IRAM 30-m telescope line survey
3 mm 79750-115750 MHz Lines with TAgt0.04 K
2152 504 are U 23 2 mm130000-178000 MHz
Lines with T gt 0.1 K 4031 1606 are U
40 1mm196750-281000 MHz Líneas con Tgt0.1 K
7676 lines 3281 are U 43
6
  • Large fraction of U lines most likely
    corresponds to isotopologues and vibrational
    excited states of well known molecules like
    CH3OCH3, CH3OH, methyl formate
  • To identify lines unambiguously we need to know
    their frequencies and intensities at the
    temperature of the observed interstellar region
  • To predict the intensity we need to know the
    lower state energy and the transition dipole
    moment matrix element
  • The proposed scheme allows us to make spectral
    predictions without assignment or analysis

7
Bootstrap Analysis of A and E Ground State
Lines of Methyl Formate
But this is only about 10 of lines
8
Prediction scheme
  • Measure spectrum of the molecule at two
    temperatures
  • Ratio the intensities of all spectral lines
  • Given the lower state energy of a single
    previously assigned transition we can calculate
    lower state energies and relative intensities at
    the desired sample temperature for the frequency
    region where power profile of the spectrometer is
    known

9
Absorption Coefficients What You Need to Know
to Simulate Spectra at an Arbitrary Temperature
T3 without Spectral Assignment
  • The total number density (chemistry and pressure
    issues).
  • But, for an unassigned line, one does not know
  • -The matrix element
  • -The lower state energy
  • -The partition function

10
Consider two lines, one assigned and one unknown
at two temperatures T1 and T2
Eqn. 1
  • Step 1 With Eqn. 1 for both the known and
    unknown line, we have two equations and two
    unknowns
  • 1. The number density and partition function
    ratio for the T1 and T2 lab measurements
  • 2. The lower state energy of the unassigned
    line
  • Step 2 Solve for the lower state energy of
    unassigned line

Eqn. 2
11
Comparison of Energy Levels Calculated from
Experimental and Quantum Calculations for SO2
12
Comparison of Energy Levels Calculated from
Experimental and Quantum Calculations for SO2
13
The Combined Equation
14
Comparison of Intensities Calculated from
Experimental and Quantum Calculations for SO2
15
Propagation of Uncertainty (T2 300 K)
Collisional cooling
T1 77 K
T1 77 K
16
Summary and Conclusions From experimental
measurements at two temperatures T1 and T2, it is
possible to calculate spectrum (with intensities)
at an arbitrary T3. For low T3, a relatively
low T2 improves the accuracy of the calculated
spectrum. Collisional cooling provides a
general method for achieving this low T2, with 77
K convenient and suitable for all but the lowest
temperatures. FASSST is a means of obtaining
the needed data rapidly and with chemical
concentrations constant over the data collection
period.
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